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高温合金AMS-5663M-N07718

高温合金AMS-5663M-N07718

SAE Technical Standards Board Rules provide that: “This report is published by SAE to advance the state of technical and engineering sciences. The use of this report is entirely voluntary, and its applicability and suitability for any particular use, including any patent infringement arising therefrom, is the sole responsibility of the user.”SAE reviews each technical report at least every five years at which time it may be reaffirmed, revised, or cancelled. SAE invites your written comments and suggestions.Copyright © 2004 SAE InternationalAll rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted, in any form or by any means, electronic, mechanical, photocopying,recording, or otherwise, without the prior written permission of SAE.TO PLACE A DOCUMENT ORDER:Tel: 877-606-7323 (inside USA and Canada)T el: 724-776-4970 (outside USA)Nickel Alloy, Corrosion and Heat-Resistant, Bars, Forgings, and Rings52.5Ni - 19Cr - 3.0Mo - 5.1Cb (Nb) - 0.90Ti - 0.50Al - 18FeConsumable Electrode or Vacuum Induction Melted 1775 °F (968 °C) Solution and Precipitation Heat Treated(Composition similar to UNS N07718)1.SCOPE:1.1Form:This specification covers a corrosion and heat-resistant nickel alloy in the form of bars, forgings, flash welded rings, and stock for forging or flash welded rings.1.2Application:These products have been used typically for parts requiring high resistance to creep andstress-rupture up to 1300 °F (704 °C) and oxidation resistance up to 1800 °F (982 °C), but usage is not limited to such applications.2.APPLICABLE DOCUMENTS:The issue of the following documents in effect on the date of the purchase order forms a part of this specification to the extent specified herein. The supplier may work to a subsequent revision of a document unless a specific document issue is specified. When the referenced document has been cancelled and no superseding document has been specified, the last published issue of that document shall apply.2.1 SAE Publications:Available from SAE, 400 Commonwealth Drive, Warrendale, PA 15096-0001 or .AMS 2261Tolerances, Nickel, Nickel Alloy, and Cobalt Alloy Bars, Rods, and Wire AMS 2269Chemical Check Analysis Limits, Nickel, Nickel Alloys, and Cobalt AlloysAEROSPACE MATERIALSPECIFICATIONAMS 5663MIssued SEP 1965RevisedJUL 2004Superseding AMS 5663L2.1 (Continued):AMS 2371 Quality Assurance Sampling and Testing, Corrosion and Heat-Resistant Steels and Alloys, Wrought Products and Forging StockAMS 2374 Quality Assurance Sampling and Testing, Corrosion and Heat-Resistant Steel and Alloy ForgingsAMS 2750 PyrometryAMS 2806Identification, Bars, Wire, Mechanical Tubing, and Extrusions, Carbon and Alloy Steels and Corrosion and Heat-Resistant Steels and AlloysAMS 2808Identification, ForgingsAMS 7490Rings, Flash Welded, Corrosion and Heat-Resistant Austenitic Steels,Austenitic-Type Iron, Nickel, or Cobalt Alloys or Precipitation-Hardenable Alloys ARP1313 Determination of Trace Elements in High-Temperature Alloys2.2 ASTM Publications:Available from ASTM, 100 Barr Harbor Drive, P.O. Box C700, West Conshohocken, PA 19428-2959 or .ASTM E 8 Tension Testing of Metallic MaterialsASTM E 8M Tension Testing of Metallic Materials (Metric)ASTM E 10 Brinell Hardness of Metallic MaterialsASTM E 21 Elevated Temperature Tension Tests of Metallic MaterialsASTM E 103Rapid Indentation Hardness Testing of Metallic MaterialsASTM E 112Determining Average Grain SizeASTM E 139Conducting Creep, Creep-Rupture, and Stress-Rupture Tests of Metallic Materials ASTM E 292Conducting Time-for-Rupture Notch Tension Tests of MaterialsASTM E 354Chemical Analysis of High-Temperature, Electrical, Magnetic, and Other Similar Iron, Nickel, and Cobalt Alloys3.TECHNICAL REQUIREMENTS:3.1Composition:Shall conform to the percentages by weight shown in Table 1, determined by wet chemical methods in accordance with ASTM E 354, by spectrochemical methods, by the methods of ARP1313 for lead, bismuth, and selenium, or by other analytical methods acceptable to purchaser.3.1.1Determination not required for routine analysis.3.1.2Check Analysis: Composition variations shall meet the applicable requirements of AMS 2269.3.2Melting Practice:Alloy shall be multiple melted using consumable electrode practice in the remelt cycle or shall be induction melted under vacuum. If consumable electrode remelting is not performed in vacuum, electrodes which have been produced by vacuum induction melting shall be used for remelting.3.3Condition:The product shall be supplied in the following condition.3.3.1Bars: Hot or cold finished, solution and precipitation heat treated, and descaled except as specified in 3.3.1.1 and 3.3.1.2.TABLE 1 - CompositionElementmin maxCarbon -- 0.08Manganese -- 0.35Silicon-- 0.35Phosphorus -- 0.015Sulfur-- 0.015Chromium 17.0021.00Nickel50.0055.00Molybdenum2.803.30Columbium (Niobium)4.755.50Titanium 0.65 1.15Aluminum 0.200.80Cobalt-- 1.00Tantalum (3.1.1)-- 0.05Boron -- 0.006Copper -- 0.30Lead -- 0.0005 (5 ppm)Bismuth -- 0.00003 (0.3 ppm)Selenium -- 0.0003 (3 ppm)Ironremainder--`,,,```,,,,,`,,`,`,,`,,````-`-`,,`,,`,`,,`---3.3.1.1Hot finished round bars shall be ground or turned; all other hot finished bars shall be as hotfinished.3.3.1.2Cold finished round bars shall be ground or as cold finished; all other cold finished bars shall beas cold finished.3.3.2Forgings and Flash Welded Rings: Solution and precipitation heat treated and descaled.3.3.2.1Flash welded rings shall not be supplied unless specified or permitted on purchaser's partdrawing. When supplied, rings shall be manufactured in accordance with AMS 7490.3.3.3Stock for Forging or Flash Welded Rings: As ordered by the forging or flash welded ringmanufacturer.3.4Heat Treatment:Bars, forgings, and flash welded rings shall be solution and precipitation heat treated in accordance with 3.4.1 and 3.4.2; pyrometry shall be in accordance with AMS 2750.3.4.1Solution Heat Treatment: Heat to a temperature within the range 1725 to 1850 °F (941 to 1010 °C),hold at the selected temperature within ±25 °F (±14 °C) for a time commensurate withcross-sectional thickness, and cool at a rate equivalent to an air cool or faster.3.4.1.1If forgings are not to be machined all over, heat treatment shall be performed in a suitableprotective atmosphere or, when permitted by purchaser, a suitable protective coating may beapplied to the forgings in lieu of using a protective atmosphere.3.4.2Precipitation Heat Treatment: Heat to a temperature within the range 1325 to 1400 °F(718 to 760 °C), hold at the selected temperature within ±15 °F (±8 °C) for approximately 8 hours, cool at 100 °F ± 15 (56 °C ± 8) degrees per hour to a temperature within the range 1150 to 1200 °F (621 to 649 °C), hold at the selected temperature within ±15 °F (±8 °C) for approximately 8 hours, and air cool. Instead of the 100 °F (56 °C) degrees per hour cooling rate to 1150 to 1200 °F(621 to 649 °C), the product may be furnace cooled at any rate provided the time at1150 to 1200 °F (621 to 649 °C) is adjusted to give a total precipitation heat treatment time ofapproximately 18 hours.3.5Properties:The product shall conform to the following requirements:3.5.1Bars, Forgings, and Flash Welded Rings:3.5.1.1Average Grain Size: Shall be as follows, determined in accordance with ASTM E 112. In case ofdisagreement, the intercept (Heyn) procedure shall be used.--` , , , ` ` ` , , , , , ` , , ` , ` , , ` , , ` ` ` ` -` -` , , ` , , ` , ` , , ` ---3.5.1.1.1Bars and flash welded rings under 9 square inches (58 cm2) in cross-sectional area shallexhibit an average grain size of ASTM No. 5 or finer. Due to the presence of nonrecrystallizedgrains, up to 20% of the cross section of the product may have an average grain size of ASTMNo. 3 to 5, determined by the intercept method of ASTM E 112.3.5.1.1.2Bars and flash welded rings 9 to 50 square inches (58 to 323 cm2), inclusive, in cross-sectionalarea and all forgings shall exhibit an average grain size of ASTM No. 4 or finer. Due to thepresence of nonrecrystallized grains, up to 20% of the cross section of the product may havean average grain size of ASTM No. 2 to 4, determined by the intercept method of ASTM E 112.3.5.1.2Microstructure: Product shall be free of Laves phase. Banding of acicular phase and amount ofacicular phase shall conform to standards acceptable to purchaser.3.5.1.3Tensile Properties: Product, 5.0 inches (127 mm) and under in least nominal cross-sectionaldimension, shall have the following properties:3.5.1.3.1At Room Temperature: Shall be as shown in Table 2, determined in accordance withASTM E 8 or ASTM E 8M.TABLE 2A - Minimum Room Temperature Tensile Properties, Inch/Pound UnitsSpecimen OrientationTensileStrengthksiYield Strengthat 0.2% OffsetksiElongationin 4D%Reduction ofArea%Longitudinal1851501215 Long-Transverse(Forgings)1801501012Transverse(Bars)180150 6 8 TABLE 2B - Minimum Room Temperature Tensile Properties, SI UnitsSpecimen OrientationTensileStrengthMPaYield Strengthat 0.2% OffsetMPaElongationin 4D%Reduction ofArea%Longitudinal127610341215 Long-Transverse(Forgings)124110341012Transverse(Bars)12411034 6 83.5.1.3.2At 1200 °F (649 °C): Shall be as shown in Table 3, determined in accordance withASTM E 21 on specimens heated to 1200 °F ± 5 (649 °C ± 3), held at heat for not less than 20 minutes before testing, and tested at 1200 °F ± 5 (649 °C ± 3).3.5.1.3.3Longitudinal requirements of 3.5.1.3.1 and 3.5.1.3.2 apply to specimens taken with the axis approximately parallel to the grain flow, to specimens taken in the radial direction and in the tangential direction at the rim of disc forgings, and to specimens taken in the circumferential direction from flash welded rings. All other specimens shall be considered to be in the transverse direction.3.5.1.3.4Transverse tensile properties apply only to product from which a test specimen not less than 2.50 inches (63.5 mm) long can be taken.3.5.1.3.5Specific locations of specimens from forgings and flash welded rings shall be as agreed upon by purchaser and vendor.TABLE 3A - Minimum Tensile Properties at 1200 °F, Inch/Pound Units Specimen Orientation Tensile Strength ksi Yield Strength at 0.2% OffsetksiElongation in 4D %Reduction ofArea %Longitudinal 1451251215Long-Transverse (Forgings)1401251012Transverse (Bars)140125 6 8TABLE 3B - Minimum Tensile Properties at 649 °C, SI UnitsSpecimen Orientation Tensile Strength MPa Yield Strength at 0.2% OffsetMPaElongation in 4D %Reduction ofArea %Longitudinal 10008621215Long-Transverse (Forgings)9658621012Transverse (Bars)965862 6 8--`,,,```,,,,,`,,`,`,,`,,````-`-`,,`,,`,`,,`---3.5.1.4Hardness: Shall be not lower than 331 HB, or equivalent (See 8.2), determined in accordancewith ASTM E 10 or ASTM E 103. Product shall not be rejected on the basis of hardness if thetensile property requirements of 3.5.1.3.1 are acceptable, determined on specimens taken from the same sample as that with nonconforming hardness or from another sample with similarnonconforming hardness.3.5.1.5Stress-Rupture Properties at 1200 °F (649 °C): Shall be as follows; testing of notched specimensand of combination smooth-and-notched specimens shall be performed in accordance withASTM E 292 and of smooth specimens in accordance with ASTM E 139:3.5.1.5.1 A standard cylindrical combination smooth-and-notched specimen conforming to ASTM E 292,maintained at 1200 °F ± 3 (649 °C ± 2) while a load sufficient to produce an initial axial stress of100 ksi (689 MPa) or higher is applied continuously, shall not rupture in less than 23 hours. Thetest shall be continued to rupture without change of load. Rupture shall occur in the smoothsection and elongation of this section after rupture, measured at room temperature, shall be notless than 4% in 4D for product 5.0 inches (127 mm) and under in nominal diameter or leastdistance between parallel sides.3.5.1.5.2As an alternate procedure, separate smooth and notched specimens, machined from adjacentsections of the same piece, with gage sections conforming to the respective dimensions shownin ASTM E 292 may be tested individually under the conditions of 3.5.1.5.1. The smoothspecimen shall not rupture in less than 23 hours and elongation after rupture, measured atroom temperature, shall be as specified in 3.5.1.5.1. The notched specimen shall not rupture inless time than the companion smooth specimen but need not be tested to rupture.3.5.1.5.3The tests of 3.5.1.5.1 and 3.5.1.5.2 may be conducted using incremental loading. In such case,the load required to produce an initial axial stress of 100 ksi (689 MPa) or higher shall be usedto rupture or for 23 hours, whichever occurs first. After the 23 hours and at intervals of8 hours minimum, thereafter, the stress shall be increased in increments of 5.0 ksi (34.5 MPa).Time to rupture, rupture location, and elongation requirements shall be as specified in3.5.1.5.1.3.5.2Forging Stock: When a sample of stock is forged to a test coupon and solution and precipitationheat treated as in 3.4, specimens taken from the heat treated coupon shall conform to therequirements of 3.5.1.1, 3.5.1.2, 3.5.1.3, 3.5.1.4, and 3.5.1.5. If specimens taken from the stock after solution and precipitation heat treatment as in 3.4 conform to the requirements of 3.5.1.1,3.5.1.2, 3.5.1.3, 3.5.1.4, and 3.5.1.5, the tests shall be accepted as equivalent to tests of a forgedcoupon.3.5.3Stock for Flash Welded Rings: Specimens taken from the stock after heat treatment as in 3.4 shallconform to the requirements of 3.5.1.1, 3.5.1.2, 3.5.1.3, 3.5.1.4, and 3.5.1.5.3.6Quality:The product, as received by purchaser, shall be uniform in quality and condition, sound, and free from foreign materials and from imperfections detrimental to usage of the product.--` , , , ` ` ` , , , , , ` , , ` , ` , , ` , , ` ` ` ` -` -` , , ` , , ` , ` , , ` ---3.6.1Grain flow of die forgings, except in areas which contain flash-line end grain, shall follow thegeneral contour of the forging showing no evidence of reentrant grain flow.3.7Tolerances:Bars shall conform to all applicable requirements of AMS 2261.4.QUALITY ASSURANCE PROVISIONS:4.1Responsibility for Inspection:The vendor of the product shall supply all samples for vendor's tests and shall be responsible for the performance of all required tests. Purchaser reserves the right to sample and to perform anyconfirmatory testing deemed necessary to ensure that the product conforms to specifiedrequirements.4.2Classification of Tests:4.2.1Acceptance Tests: The following requirements are acceptance tests and shall be performed oneach heat or lot as applicable:4.2.1.1Composition (3.1) of each heat.4.2.1.2Average grain size (3.5.1.1), tensile properties (3.5.1.3), hardness (3.5.1.4), and stress-ruptureproperties (3.5.1.5) of each lot of bars, forgings, and flash welded rings.4.2.1.3Microstructure (3.5.1.2) of each lot.4.2.1.4Tolerances (3.7) of bars.4.2.2Periodic Tests: Tests of forging stock (3.5.2) and of stock for flash welded rings (3.5.3) to --`,,,```,,,,,`,,`,`,,`,,````-`-`,,`,,`,`,,`---demonstrate ability to develop required properties and of grain flow of die forgings (3.6.1) areperiodic tests and shall be performed at a frequency selected by the vendor unless frequency of testing is specified by purchaser.4.3Sampling and Testing:Shall be as follows:4.3.1Bars, Flash Welded Rings, and Stock for Forging or Flash Welded Rings: In accordance withAMS 2371.4.3.2Forgings: In accordance with AMS 2374.4.4Reports:4.4.1The vendor of bars, forgings, and flash welded rings shall furnish with each shipment a reportshowing the results of tests and relevant information:4.4.1.1For each heat:Composition4.4.1.2For each lot:Average grain sizeMicrostructure resultsRoom temperature tensile properties1200 °F (649 °C) tensile propertiesHardnessStress-rupture properties.4.4.1.3 A statement that the product conforms to the other technical requirements.4.4.1.4Purchase order numberHeat and lot numbersAMS 5663MSizeQuantity.4.4.1.5If forgings are supplied, the size and melt source of stock used to make the forgings.4.4.2The vendor of stock for forging or flash welded rings shall furnish with each shipment a reportshowing the results of tests for the composition of each heat. This report shall include the purchase order number, heat and lot number, AMS 5663M, size, and quantity.4.5Resampling and Retesting:Shall be as follows:4.5.1Bars, Flash Welded Rings, and Stock for Forging or Flash Welded Rings: In accordance withAMS 2371.4.5.2Forgings: In accordance with AMS 2374.5.PREPARATION FOR DELIVERY:5.1Sizes:Except when exact lengths or multiples of exact lengths are ordered, straight bars will be acceptable in mill lengths of 6 to 24 feet (1.8 to 7.3 m) but not more than 25% of any shipment shall be supplied in lengths of 6 to 9 feet (1.8 to 2.7 m) except that for bars weighing over 25 pounds per foot(37 kg/m), short lengths down to 2 feet (610 mm) may be supplied.5.2Identification:Shall be as follows:5.2.1Bars: In accordance with AMS 2806.5.2.2Forgings: In accordance with AMS 2808.5.2.3Flash Welded Rings and Stock for Forging or Flash Welded Rings: As agreed upon by purchaserand vendor.5.3Packaging:The product shall be prepared for shipment in accordance with commercial practice and incompliance with applicable rules and regulations pertaining to the handling, packaging, andtransportation of the product to ensure carrier acceptance and safe delivery.6.ACKNOWLEDGMENT:A vendor shall mention this specification number and its revision letter in all quotations and whenacknowledging purchase orders.7.REJECTIONS:Product not conforming to this specification, or to modifications authorized by purchaser, will be subject to rejection.8.NOTES:8.1 A change bar (|) located in the left margin is for the convenience of the user in locating areas wheretechnical revisions, not editorial changes, have been made to the previous issue of a specification.An (R) symbol to the left of the document title indicates a complete revision of the specification, including technical revisions. Change bars and (R) are not used in original publications, nor inspecifications that contain editorial changes only.8.2Hardness conversion tables for metals are presented in ASTM E 140.8.3Terms used in AMS are clarified in ARP1917.--` , , , ` ` ` , , , , , ` , , ` , ` , , ` , , ` ` ` ` -` -` , , ` , , ` , ` , , ` ---AMS 5663M SAE AMS 5663M- 11 -8.4Dimensions and properties in inch/pound units and the Fahrenheit temperatures are primary;dimensions and properties in SI units and the Celsius temperatures are shown as the approximate equivalents of the primary units and are presented only for information.8.5Purchase documents should specify not less than the following:AMS 5663MForm and size or part number of product desiredQuantity of product desiredIf applicable, specific location of tensile specimens from forgings and flash welded rings (See 3.5.1.3.5).8.6Key Words:UNS N07718, solution heat treated, precipitation heat treated, bars, forgings, rings, stress-rupture, grain size, microstructure, 1200 °F tensilePREPARED UNDER THE JURISDICTION OF AMS COMMITTEE “F”Copyright SAE InternationalProvided by IHS under license with SAELicensee=Parker Hannifin - Categories/5936628103 Not for Resale, 08/31/2006 16:59:08 MDT No reproduction or networking permitted without license from IHS --`,,,```,,,,,`,,`,`,,`,,````-`-`,,`,,`,`,,`---。

AMS A-8625

AMS A-8625

SAE Technical Standards Board Rules provide that: “This report is published by SAE to advance the state of technical and engineering sciences. The use of this report is entirely voluntary, and its applicability and suitability for any particular use, including any patent infringement arising therefrom, is the sole responsibility of the user.”SAE reviews each technical report at least every five years at which time it may be reaffirmed, revised, or cancelled. SAE invites your written comments and suggestions.Copyright © 2003 SAE InternationalAll rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted, in any form or by any means, electronic, mechanical, photocopying,recording, or otherwise, without the prior written permission of SAE.TO PLACE A DOCUMENT ORDER:Tel: 877-606-7323 (inside USA and Canada)Tel: 724-776-4970 (outside USA)Anodic Coatings for Aluminum and Aluminum AlloysCANCELLATION NOTICEThis specification has been declared “CANCELLED” by the Aerospace Materials Division, SAE, as of July, 2003, and has been superseded by MIL-A-8625. The requirements of the latest issue of MIL-A-8625 shall be fulfilled whenever reference is made to the cancelled AMS-A-8625. By this action, this document will remain listed in the Numerical Section of the index of Aerospace Materials Specifications noting that it is superseded by MIL-A-8625. Cancelled specifications are available from SAE upon request.AEROSPACE MATERIALSPECIFICATIONAMS-A-8625AIssued JUL 2000CancelledJUL 2003Superseding AMS-A-8625NOTICEThis document has been taken directly from U.S. Military Specification MIL-A-8625F and contains only minor editorial and format changes required to bring it into conformance with the publishingrequirements of SAE technical standards. The initial release of this document is intended to replace MIL-A-8625F. Any part numbers established by the original specification remain unchanged.The original Military Specification was adopted as an SAE standard under the provisions of the SAE Technical Standards Board (TSB) Rules and Regulations (TSB 001) pertaining to accelerated adoption of government specifications and standards. TSB rules provide for (a) the publication of portions of unrevised government specifications and standards without consensus voting at the SAE Committee level, and (b) the use of the existing government specification or standard format.Under Department of Defense policies and procedures, any qualification requirements and associated qualified products lists are mandatory for DOD contracts. Any requirement relating to qualified products lists (QPL’s) has not been adopted by SAE and is not part of this SAE technical document.--``,,``,`,`,,,,,`,`,,``,,,``,,-`-`,,`,,`,`,,`---1.SCOPE:1.1Scope:This specification covers the requirements for six types and two classes of electrolytically formed anodic coatings on aluminum and aluminum alloys for non-architectural applications (see 6.1).1.2Classification:The anodic coating Types and Classes covered by this specification are as specified herein (see 6.2 and 6.21).1.2.1Types:Type I -Chromic acid anodizing, conventional coatings produced from chromic acid bath (see3.4.1)Type IB - Chromic acid anodizing, low voltage process, 22 ± 2V, (see 3.4.1)Type IC -Non-chromic acid anodizing, for use as a non-chromate alternative for type I and IBcoatings (see 3.4.1 and 6.1.2)Type II -Sulfuric acid anodizing, conventional coatings produced from sulfuric acid bath (see3.4.2)Type IIB -Thin sulfuric acid anodizing, for use as a non-chromate alternative for Type I and IB coatings (see 3.4.2 and 6.1.2)Type III -Hard Anodic Coatings (see 3.4.3)1.2.2Classes:Class 1 - Non-dyed (see 3.5.)Class 2 - Dyed (see 3.6.)2.APPLICABLE DOCUMENTS:The following specifications and standards form a part of this document to the extent specified herein.2.1U.S. Government Publications:Available from DODSSP, Subscription Services Desk, Building 4D, 700 Robbins Avenue,Philadelphia, PA 19111-5094.MIL-P-23377Primer Coating, Epoxy-Polyamide, Chemical and Solvent ResistantMIL-C-81706Chemical Conversion Materials for Coating Aluminum and Aluminum Alloys MIL-P-85582Primer Coatings: Epoxy, WaterborneQQ-A-250/4Aluminum Alloy 2024, Plate and Sheet --` ` , , ` ` , ` , ` , , , , , ` , ` , , ` ` , , , ` ` , , -` -` , , ` , , ` , ` , , ` ---2.1 (Continued):FED-STD-141Paint, Varnish, Lacquer, and Related Materials: Methods for Sampling andTestingFED-STD-151Metals; Test MethodsMIL-STD-105Sampling Procedures and Tables for Inspection by Attribute2.2ASTM Publications:Available from ASTM, 100 Barr Harbor Drive, West Conshohocken, PA 19428-2959.ASTM B 117Method of Salt Spray (Fog) TestingANSI/ASTM B 137Weight of Coating on Anodically Coated Aluminum, Measurement ofASTM B 244Thickness of Anodic Coatings on Aluminum and of Other NonconductiveCoatings on Nonmagnetic Basis Metals with Eddy Current Instruments,Measurement ofASTM D 822Light and Water Exposure Apparatus (Carbon-Arc Type) for Testing Paint,Varnish, Lacquer and Related Products, Standard Practice for Operating ASTM D 2244Color Differences of Opaque Materials, Instrumental Evaluation ofASTM G 23Standard Practice for Operating Light Exposure Apparatus (Carbon-Arc Type)With and Without Water for Exposure of Non-metallic Materials ASTM G 26Operating Light-Exposure Apparatus (Xenon-Arc Type) With and WithoutWater for Exposure of Non-metallic materials3.REQUIREMENTS:3.1Materials:The materials used shall be such as to produce coatings which meet the requirements of thisspecification.3.1.1Base metal: The base metal shall be free from surface defects, caused by machining, cutting,scratching, polishing, buffing, roughening, bending, stretching, deforming, rolling, sandblasting, vaporblasting, etching, heat treatment condition, alloy chemistry imbalance and inclusions, that will cause coated test panels or parts to fail any of the requirements of this specification. The base metal shall be subjected to cleaning, etching, anodizing and sealing procedures as necessary to yield coatings meeting all requirements of this specification.3.2Equipment and processes:The equipment and processes employed shall be such as to produce coatings which meet therequirements of this specification. Unless otherwise specified in the contract, purchase order or applicable drawing (see 6.2), process operating conditions shall be at the option of the supplier.--` ` , , ` ` , ` , ` , , , , , ` , ` , , ` ` , , , ` ` , , -` -` , , ` , , ` , ` , , ` -----``,,``,`,`,,,,,`,`,,``,,,``,,-`-`,,`,,`,`,,`---AMS-A-8625A SAE AMS-A-8625A3.3General:3.3.1Anodizing of parts and assemblies:3.3.1.1Anodizing of parts: Unless otherwise specified in the contract, purchase order or applicabledrawing (see 6.2), parts shall be anodized after all heat treatment, machining, welding, forming and perforating have been completed.3.3.1.2Anodizing of assemblies: Unless otherwise specified in the contract, purchase order orapplicable drawing, anodic coatings shall not be applied to assemblies which will entrap theelectrolyte in joints or recesses (components shall be anodized separately prior to assembly).When anodizing of assemblies is authorized by the contract, purchase order or applicabledrawing, the processing method used shall not result in subsequent damage to the assemblyfrom electrolyte entrapment (Type I or IA coatings shall be used unless another coating Type is specified). Assemblies which contain non-aluminum parts such as steel, brass or organicsubstances, which would be attacked by pretreatment or anodizing solutions or would preventuniform formation of the anodic coating, shall not be anodized as assemblies, unless the non-aluminum surfaces are masked or electrically insulated in a manner which produces anodiccoatings meeting the requirements of this specification.3.3.1.2Anodizing of complex shapes: When anodizing complex shapes which will entrap the electrolytein recesses, the processing method used shall not result in subsequent damage to the part from electrolyte entrapment (Type I or IA coatings shall be used unless another coating Type isspecified).3.3.2Handling and cleaning: Parts shall be so handled during all pretreatments, anodizing and posttreatments that mechanical damage or contamination will be avoided. Parts shall be free of allforeign substances, oxides and soils, such as greases, oil, paint and welding flux. Parts shall have oxide and other interfering films removed by the use of proper cleaning procedures so as to beclean and have water break free surfaces. Abrasives containing iron, such as steel wool, ironoxide rouge and steel wire, which may become embedded in the metal and accelerate corrosion of aluminum and aluminum alloys, are prohibited as a means of mechanical cleaning, prior toanodizing. If special cleaning requirements are required they shall be specified in the contract or purchase order (see 6.2).3.3.3Reflective surfaces: When specified in the contract or purchase order (see 6.2), parts fabricated toproduce a highly reflective surface shall be chemically or electrochemically brightened, prior toanodic coating (see 6.9).3.3.4Touch up (mechanical damage and contact marks): Unless otherwise specified (see 6.2),mechanically damaged areas from which the anodic coating has been removed without damage to the part may be touched up using chemical conversion materials approved on QPL-81706 forClass 1A coatings and the applicable method of application. Touch up shall apply only toinadvertent mechanical damage such as scratch marks. For Type III coatings, touch up shall only be allowed in areas which will not be subjected to abrasion (see 6.1.1). The mechanicallydamaged area(s) shall not exceed 5 percent of the total anodized area of the item or touch up shall not be permitted. When specified in the contract or purchase order (see 6.2), contact marks shall be touched up using the above method required for mechanical damage.3.4Coatings:Conventional anodic coatings as specified in the contract, purchase order or applicable drawings (see 6.2), shall be prepared by any process or operation to produce the specified coating onaluminum and aluminum alloys.3.4.1Type I, IB, and IC coatings: Type I and IB coatings shall be the result of treating aluminum andaluminum alloys electrolytically in a bath containing chromic acid to produce a uniform anodiccoating on the metal surface. Type IC coatings shall be the result of treating aluminum andaluminum alloys electrolytically in a bath containing mineral or mixed mineral/organic acids (non-chromic acid) to produce a uniform anodic coating on the metal surface. Unless otherwise --``,,``,`,`,,,,,`,`,,``,,,``,,-`-`,,`,,`,`,,`---specified in the contract, purchase order or applicable drawing, Type I coatings shall not be applied to aluminum alloys with a nominal copper content in excess of 5.0 percent; nominal siliconcontents in excess of 7.0 percent; or when the total allowable contents of nominal alloyingelements exceed 7.5 percent. Heat treatable alloys which are to receive a Type I, IB, or IC coating shall be in the required temper to receive a Type I, IB, or IC coating shall be in the required temper obtained by heat treatment, such as -T4, -T6, or T73, prior to anodizing.3.4.1.1Type IC coatings: Type IC coatings provide a non-chromate alternative to Type I and IB coatings.Unless approved by the procuring activity, substitution of a Type IC coating where Type I or IB is specified shall be prohibited.3.4.2Type II and IIB coatings: Type II and IIB coatings shall be the result of treating aluminum andaluminum alloys electrolytically in a bath containing sulfuric acid to produce a uniform anodiccoating on the metal surface. Heat treatable alloys shall be in the required temper obtained byheat treatment, such as -T4, -T6, or T73, prior to anodizing.3.4.2.1Type IIB coatings: Type IIB coatings provide a non-chromate alternative to Type I and IBcoatings. Unless approved by the procuring activity, substitution of a Type IIB coating whereType I or IB is specified shall be prohibited.3.4.3Type III coatings: Type III coatings shall be the result of treating aluminum and aluminum alloyselectrolytically to produce a uniform anodic coating on the metal surface. Type III coatings shall be prepared by any process operation to produce a heavy dense coating of specified thickness on aluminum alloys (see 3.7.2.1). Unless otherwise specified in the contract, purchase order orapplicable drawing, Type III coatings shall not be applied to aluminum alloys with a nominal copper content in excess of 5 percent or a nominal silicon content in excess of 8.0 percent. Alloys with a nominal silicon content higher than 8.0 percent may be anodized subject to approval of theprocuring activity. Heat treatable alloys shall be in a temper obtained by heat treatment, such as -T4, -T6, or T73, prior to anodizing.3.5Class 1:When class 1 is specified in the contract or purchase order, (see 6.2), the anodic coating shall not be dyed or pigmented. Any natural coloration resulting from anodic treatment with the various alloy compositions shall not be considered coloration. The characteristic color imparted by the sealing process shall also be considered as non-dyed.3.6Class 2:When class 2 is specified in the contract or purchase order, (see 6.2), the anodic coating shall be uniformly dyed or pigmented by exposure to a solution of a suitable type dye or stain. The color on wrought alloys shall be uniform. Cast alloys may exhibit dye bleed-out or lack of color (or color uniformity) associated with the inherent porosity of the casting. The dyes and pigments used shall not be damaging to the anodic coatings.3.6.1Dye color: When dyed or pigmented coatings are required, the color and color uniformityrequirements shall be as specified on the contract, purchase order or applicable drawing (see 6.2).3.6.1.1Casting alloys: Dyed casting alloys may show a slight lack of color uniformity. The degree ofnon-uniformity that is acceptable shall be established by the procuring activity (see 6.2).3.7Detail requirements:3.7.1Types I, IB, IC, II, and IIB coatings:3.7.1.1Weight of coating: Prior to dyeing or sealing, Type I, IB, IC, II, and IIB coatings shall meet thecoating weight requirements of Table I when tested in accordance with 4.5.2 (see 6.10.6).TABLE I. Types I, IB, IC, II, and IIB unsealed anodic coating weights3.7.1.2Corrosion resistance: After exposure to the salt spray test specified in4.5.3, specimens shall bevisually examined to determine that all of the following conditions are met:a.Test specimens shall show no more than a total of 15 isolated pits (see 6.19), none largerthan 0.031 inch in diameter, in a total of 150 square inches of test area grouped from five ormore test pieces. Areas within 0.062 inch from identification markings, edges and electrodecontact marks remaining after processing shall be excluded.b.Test specimens shall show no more than 5 isolated pits, none larger than 0.031 inch indiameter, in a total of 30 square inches from one or more test pieces. Areas within 0.062 inchfrom identification markings, edges and electrode contact marks remaining after processingshall be excluded.c.In addition to the requirements in (a) and (b) above, Type I and IB test specimens shall notexhibit patchy dark gray areas (spots, streaks, or marks).3.7.1.3Light fastness resistance: Class 2, dyed anodic coatings, shall show no more fading ordiscoloration than would be equivalent to a Delta (E) value of 3 when subjected to the lightfastness resistance test (see 4.5.4), unless otherwise specified in the contract or purchase order (see 6.2). Light fastness resistance shall be determined only when specified in the contract,purchase order or applicable drawing (see 6.2).3.7.1.4Paint adhesion: When tested in accordance with4.5.6, no intercoat separation shall occurbetween the paint system and the anodic coating or between the anodic coating and the basemetal. Paint adhesion shall be determined only when specified in the contract, purchase order or applicable drawing (see 6.2).3.7.2Type III coatings:3.7.2.1Thickness of coating: Unless otherwise specified in the contract, purchase order, or applicabledrawing (see 6.2), the nominal thickness of the coating shall be 0.002 inch (2 mils) (see 6.16,6.17 and 6.10 through 6.10.5). Unless otherwise specified, the thickness of the coating shall notvary by more than ± 20 percent for coatings up to 0.002 inches thick (2 mils) when tested inaccordance with 4.5.1. Coatings over 0.002 inches (2 mils) shall not vary by more than ± 0.0004 inches (0.4 mils) in thickness. A typical Type III coating thickness range is shown in Table IV.3.7.2.1.1Weight of coating: The coating weight may be determined in lieu of the coating thickness (see 3.7.2.1), at the option of the procuring activity. Unsealed Type III coatings shall have a minimum coating weight of 4320 milligrams per square foot for every 0.001 inch of coating when tested in accordance with 4.5.2 (see 6.2).3.7.2.2Abrasion resistance: When tested in accordance with 4.5.5, unsealed Type III coatings shall provide a hard abrasion resistant finish as specified herein (see 6.17). The anodic coating shall have a maximum wear index of 3.5 mg/1000 cycles on aluminum alloys having a copper content of 2 percent or higher (see 6.13). The wear index for all other alloys shall not exceed 1.5 mg/1000 cycles.3.8Sealing:3.8.1Types I, IB, IC, II, and IIB: All Types I, IB, IC, II, and IIB anodic coatings shall be completely sealed, unless otherwise specified in the contract, purchase order or applicable drawing (see 6.2). They shall be sealed in accordance with 3.8.1.1 or 3.8.1.2 as applicable. If wetting agents are used they shall be of the non-ionic type.3.8.1.1Class 1: When class 1 is specified, sealing shall be accomplished by immersion in a sealing medium such as a 5 percent aqueous solution of sodium or potassium dichromate (pH 5.0 to 6.0) for 15 minutes at 90°C to 100°C (194°F to 212°F), in boiling deionized water, cobalt or nickel acetate, or other suitable chemical solutions (see 6.15).3.8.1.2Class 2: When class 2 is specified, sealing shall be accomplished after dyeing by immersion in a sealing medium, such as a hot aqueous solution containing 0.5 percent nickel or cobalt acetate (pH 5.5 to 5.8), boiling deionized water, duplex sealing with hot aqueous solutions of nickel acetate and sodium dichromate (see 6.11), or other suitable chemical solutions.3.8.2Type III: Type III coatings shall not be sealed where the main function of application is to obtain the maximum degree of abrasion or wear resistance. Where Type III coatings are used for exterior non-maintained applications requiring corrosion resistance but permitting reduced abrasionresistance, the contract or purchase order shall specify that sealing is required. Sealing for such Type III coatings shall be accomplished by immersion in a medium, such as boiling deionizedwater, in a hot aqueous 5 percent sodium dichromate solution, in a hot aqueous solution containing nickel or cobalt acetate or other suitable chemical solutions (see 6.2). When Type III coatings are provided unsealed, parts shall be thoroughly rinsed in cold, clean water and dried after anodizing.3.9Dimensions of coated articles:Articles or parts shall comply with the dimensional requirements of the applicable drawings after application of the anodic coating (see 6.10.1). (For interference in close fits of parts or assemblies see 6.10.5).--``,,``,`,`,,,,,`,`,,``,,,``,,-`-`,,`,,`,`,,`---3.10Toxicity:The coatings and electrical/chemical processes used to develop these anodic coatings shall have no adverse effect on the health of personnel when used for their intended purposes. Questionspertinent to this effect shall be referred by the contracting activity to the appropriate departmental medical service who will act as an advisor to the contracting agency.3.11Painting/coating:Painting/coating operations shall be performed as soon as practical after the anodizing process on clean coatings. If parts require storage prior to painting/coating, they shall be stored in a manner that will avoid contamination. If the parts become contaminated, they shall be cleaned in a manner that will not be detrimental to the anodic coating or the base metal (see 6.3).3.12Dyeing or coloring:Anodic coatings shall not be allowed to dry before dyeing or coloring. Items to be dyed or colored should be preferably coated by the Type II anodizing treatment (see 6.12). Dyed or colored coatings shall not be allowed to remain in rinse waters for more than 5 minutes before sealing.3.13Workmanship:Except for touch up areas in accordance with 3.3.4 and as noted below, the applied anodic coating shall be continuous, smooth, adherent, uniform in appearance, free from powdery areas, loose films, breaks, scratches and other defects which will reduce the serviceability of anodized parts orassemblies. Differences in anodic coating appearance resulting from inherent base metaldifferences in a component such as the presence of welds, components containing cast andmachined surfaces, and differences in grain size within a forging shall not be cause to reject the anodic coating unless otherwise specified in the contract or purchase order (see 6.2). Slightdiscoloration from dripping or rundown of the sealing solution from designed crevices in acomponent shall be allowed.3.13.1Contact marks: The size and number of contact marks shall be at a minimum consistent with goodpractice (see 6.14). If a specific location for contact marks is desired, the location shall bespecified on the contract or purchase order (see 6.2).4.QUALITY ASSURANCE PROVISIONS:4.1Responsibility for inspection:Unless otherwise specified in the contract or purchase order, the contractor is responsible for the performance of all inspection requirements (examinations and tests) as specified herein. Except as otherwise specified in the contract or purchase order, the contractor may use his own or any other facilities suitable for the performance of the inspection requirements specified herein, unlessdisapproved by the Government. The Government reserves the right to perform any of theinspections set forth in the specification where such inspections are deemed necessary to ensure supplies and services conform to prescribed requirements.--``,,``,`,`,,,,,`,`,,``,,,``,,-`-`,,`,,`,`,,`---4.1.1Responsibility for compliance: All items must meet all requirements of Section 3. The inspectionset forth in this specification shall become a part of the contractor’s overall inspection system or quality program. The absence of any inspection requirements in the specification shall not relieve the contractor of the responsibility of ensuring that all products or supplies submitted to theGovernment for acceptance comply with all requirements of the contract. Sampling inspection, as part of manufacturing operations, is an acceptable practice to ascertain conformance torequirements, however, this does not authorize submission of known defective material, eitherindicated or actual, nor does it commit the Government to acceptance of defective material.4.2Classification of inspection:The inspection requirements specified herein are classified as follows:a.Process control inspection (see 4.3).b.Quality conformance inspection (see 4.4).4.3Process control inspection:--``,,``,`,`,,,,,`,`,,``,,,``,,-`-`,,`,,`,`,,`---4.3.1Process control document (PCD): The anodizer shall develop, maintain, and adhere to a PCDdescribing the anodizing process and procedures used to meet the requirements of thisspecification. As a minimum, the PCD shall describe the following:-All steps in the processing sequence.-Ranges for immersion time and temperature for each step in the process.-Chemical constituents used and allowable solution control ranges to be used for solution analysis (see 4.3.2) for each step in the process.-Ranges for temperature, current density and anodizing time (or voltage ramps and hold times) as applied to individual alloys or alloy series.4.3.2Solution analysis: Solution analysis shall be performed on all the processing solutions in theanodizing line to determine if the solution controls are within the acceptable ranges established in the PCD (see 4.3.1). Solution analysis shall be performed at least once every two weeks unless otherwise specified by the procuring activity. The processor shall maintain a record of the history of each processing bath, showing all chemicals or treatment solutions added to the baths and the results of all chemical analysis performed. Upon request of the procuring activity, such records, as well as reports of the test results, shall be made available. These records shall be maintained for not less than one year after completion of the contract or purchase order.4.3.3Process control tests: To assure continuous control of the process, specimens shall be tested inaccordance with Table II. Process control tests are conducted to determine conformance of the anodic coatings with the requirements of this specification and are acceptable as evidence of the properties being obtained with the equipment and procedures employed.4.3.3.1Frequency of the process control tests: Process control tests shall be conducted at least onceevery month. In addition, the intervals between each monthly test shall not exceed 35 days. Ifproduction in accordance with this specification is not performed for a periodic of one month or longer, process control tests shall be conducted at the start of production.TABLE II. Process control tests4.3.3.2Process control test specimens: Production parts shall be used for process control inspectionprovided they can be adapted to the applicable test. If the production parts can not be adapted toa particular test, test panels shall be used. At the option of the supplier, test panels shall becomposed of either 2024-T3 per QQ-A-250/4 or the alloy representing the largest percent of work anodized during the monthly process control period. Whenever possible, the specimen panelsshall be anodized with an actual production run. Additional details for the specimen panels shall be as specified in 4.3.3.2.1 through 4.3.3.2.4.4.3.3.2.1Test specimens for coating weight: Coating weight shall be determined on undyed andunsealed production parts or specimen panels (see 4.3.3.2). When specimen panels are used,they shall have a minimum width of 3 inches, a minimum length of 3 inches, and a minimumnominal thickness of 0.032 inches.4.3.3.2.2Test specimens for coating thickness: Coating thickness shall be determined on Type IIIproduction parts or specimen panels (see 4.3.3.2). When specimen panels are used, they shallhave a minimum width of 3 inches, a minimum length of 3 inches, and a minimum nominalthickness of 0.032 inches.4.3.3.2.3Test specimens for corrosion and light fastness resistance: Corrosion resistance shall bedetermined on dyed (Class 2 only) and sealed production parts or specimen panels (see4.3.3.2). Light fastness testing is performed only on dyed (Class 2) coatings and only whenspecified (see 6.2). When specimen panels are used, they shall have a minimum width of 3inches, a minimum length of 10 inches, and a minimum nominal thickness of 0.032 inches. 4.3.3.2.4Test specimens for abrasion resistance: Abrasion resistance shall be determined on Type IIIproduction parts or specimen panels (see 4.3.3.2). When specimen panels are used, they shallhave a width of 4 inches, a length of 4 inches, and a minimum nominal thickness of 0.063inches.。

国外访学心得体会

国外访学心得体会

国外访学心得体会范文一在美国的游学历程中,我用以下五个部分来简述归纳我的体会。

我的选择是华盛顿大学,在西雅图。

选学校的时候还是一二月份的事情,后来因为《北京遇上西雅图》的走红,本来并不算特别的一个选择,倒成了颇具意境的一个行程,于是我们上演了一次《北大遇上西雅图》,我也便用这个作为感想的题目。

一、学习体会我们在华盛顿大学的Foster商学院进行交换访学,老实说,短期的访学要学到太多东西是不现实的,更多的是体验不同的文化、方式、感受。

与北大光华相比较,其实国外的商学院从教授、教授内容等方面不一定有质的差别。

但是从西方的沟通习惯,教室直接是U字形排布,教授走到学生中间;鼓励思考鼓励对话;即时互动积极探讨没有正确答案等等方面,确实是一种不同的文化和方式,很好的鼓励了大家独立思考。

我们就是在这样的氛围中,体会了国外的MBA教学。

课堂中,教授们随时可能发起互动游戏,让同学的在参与中体验和分享,并鼓励同学们非常独立的思维,不受束缚,这可能是最深刻的一个感受。

同时,大家用极短的时间,分组完成了美国一个著名服装品牌A&F (就是那个著名的肌肉男赤裸上身招揽顾客的牌子)进军亚洲市场的案例。

这些案例的分析,没有对错,只讲逻辑和方法,美国的孩子从很小的时候就经历这样的思维锻炼,因此确实更加思维活跃和开放。

二、企业参观访学安排中另一重要内容是企业参观。

西雅图虽然并非美国最繁华的的城市,但是是美国最宜居的城市,同样集中了不少美国著名企业,其中最有名的四大企业总部是波音、星巴克、亚马逊、微软。

访学的正式安排我们走进了波音、星巴克,还跟随同学驱车到了微软的总部。

还是那句话,更多的体验教给你更多的生活。

在波音,我们主要体会了大工业时代,人类挑战极限的恢弘,而在星巴克,则是一个咖啡文化和星巴克文化之旅,用各种方式让你体验其文化内涵。

三、美式生活既然在美国居住,自然有机会体验美国人的生活。

除了体验吃、环境、购物外,我最大的收获周三意外发现的一个在UniversityVillage 举办的社区Party,比如美国人那种对生活的积极参与的态度,沉浸在音乐中欢快的起舞,非常自由的享受生活。

航空复合材料螺旋桨叶片制造工艺研究进展

航空复合材料螺旋桨叶片制造工艺研究进展

引用格式:武珈羽,杨金水,陈丁丁,等. 航空复合材料螺旋桨叶片制造工艺研究进展[J]. 航空材料学报,2024,44(2):104-116.WU Jiayu,YANG Jinshui,CHEN Dingding,et al. Research progress in manufacturing technology of aviation composite propeller blade[J]. Journal of Aeronautical Materials,2024,44(2):104-116.航空复合材料螺旋桨叶片制造工艺研究进展武珈羽, 杨金水*, 陈丁丁, 郭书君, 尹昌平(国防科技大学 空天科学学院 材料科学与工程系,长沙 410073)摘要:螺旋桨推进方式在航空领域占有重要地位。

复合材料具有高比强度、高比模量、高阻尼、可设计性等特性,复合材料螺旋桨叶片能够提升螺旋桨减重效率、推进效率、耐蚀性、降噪等方面性能,已成为大势所趋。

本文对国内外航空复合材料螺旋桨叶片的研究成果进行回顾和总结,基于传统飞机螺旋桨叶片和旋翼桨叶,对航空螺旋桨叶片材料体系、结构设计和制造工艺进行分类阐述,重点总结复合材料螺旋桨制造工艺中的关键技术问题,概述桨叶制造工艺方面的仿真模拟研究,最后从健全材料体系、优化结构设计、深入工艺研究和加强数值模拟技术的工程化应用几个方面提出了国产化复合材料航空螺旋桨的未来发展方向。

关键词:复合材料;螺旋桨叶片;复合材料螺旋桨;成型工艺doi:10.11868/j.issn.1005-5053.2023.000042中图分类号:V258 文献标识码:A 文章编号:1005-5053(2024)02-0104-13Research progress in manufacturing technology of aviationcomposite propeller bladeWU Jiayu, YANG Jinshui*, CHEN Dingding, GUO Shujun, YIN Changping (Department of Material Science and Engineering,College of Aerospace Science and Engineering,National University of Defense Technology,Changsha 410073,China)Abstract: Propeller propulsion technology plays an important role in aviation field. Composite materials have the characteristics of high specific strength,high specific modulus,high damping,designability and so on. The use of composite material propeller blades can further improve the performance of propeller in terms of mass reduction efficiency,propulsion efficiency,corrosion resistance,noise reduction. Composite material propeller blades have become the general trend. Based on aircraft propeller blades and rotor blades,this paper aims to perform a brief review of the research achievements of aviation composite propeller blades at home and abroad,classifies and expounds the material systems,structural design and molding processes of aviation propellers. The key technical problems and the simulation research on manufacturing process of propeller at home and abroad are summarized. Finally,the future development direction of domestic composite propellers from the aspects of improving the material system,optimizing the structure design,deepening the process research and strengthening the engineering application of numerical simulation technology are concluded.Key words: composite material;propeller blade;composite propeller;molding process螺旋桨是一种通过把流动介质向后推去而使桨叶产生反方向力的推进装置。

天宇航天新材料产品手册

天宇航天新材料产品手册

天宇航天新材料产品手册As I started flipping through the pages of the Tianyu Aerospace New Materials Product Catalog, I couldn't help but feel a sense of awe at the innovative products and advanced technologies presented within. 这个产品手册呈现了许多创新产品和先进技术,让我不禁感到惊叹。

From cutting-edge composites to revolutionary coatings, Tianyu Aerospace is leading the way in developing materials that are essential for the future of space exploration. 天宇航天领先开发的复合材料和革命性涂料等产品,为未来太空探索提供了必不可少的材料。

One aspect of the product catalog that particularly caught my attention was the section on thermal protection materials. 这个产品手册中一个特别吸引我的地方是关于热防护材料的部分。

The innovative solutions offered by Tianyu Aerospace in this area are crucial for ensuring the safety of spacecraft as they re-enter the Earth's atmosphere. 天宇航天在这一领域提供的创新解决方案对于确保太空飞船在重新进入地球大气层时的安全至关重要。

航天航空材料在羽绒服上的应用

航天航空材料在羽绒服上的应用

航天航空材料在羽绒服上的应用1.羽绒服使用航天航空材料制成,可以有效保暖和防水。

Down jackets made with aerospace materials can effectively insulate and resist water.2.轻质的航天材料使羽绒服更加舒适,不会给穿着者带来压力。

The lightweight aerospace materials make the down jacket more comfortable and do not put pressure on the wearer.3.航天航空材料在羽绒服上的运用使得服装更具有耐磨性和耐用性。

The application of aerospace materials on down jackets makes the clothing more abrasion-resistant and durable.4.羽绒服的外层材料采用航天航空材料,可以有效抵御风雨,保持穿着者干燥。

The outer layer of the down jacket is made of aerospace materials, which can effectively resist wind and rain, keeping the wearer dry.5.航天航空材料具有较好的透气性能,在羽绒服上可以增加穿着的舒适感。

Aerospace materials have good breathability and can increase the comfort of wearing down jackets.6.航天航空材料可以在极端环境下保持稳定性,为羽绒服的使用提供了更多可能。

Aerospace materials can maintain stability in extreme environments, providing more possibilities for the use of down jackets.7.羽绒服的内胆采用航天航空材料填充,可以轻盈保暖,不易形变。

关于陶瓷的英语单词

关于陶瓷的英语单词

关于陶瓷的英语单词英文回答:Ceramics is a broad term that encompasses a wide range of materials and objects made from inorganic, non-metallic compounds, most commonly oxides, carbides, nitrides, and borides. Ceramics are typically hard, brittle, and heat-resistant, and they are used in a variety of applications, including pottery, tiles, bricks, and refractories.The word "ceramics" is derived from the Greek word "keramos," which means "burnt earth." This is because many ceramics are made by heating clay or other natural materials to a high temperature. The heat causes the materials to undergo a series of chemical reactions that result in the formation of a hard, durable material.Ceramics can be divided into two main categories: traditional ceramics and advanced ceramics. Traditional ceramics are made from natural materials, such as clay,feldspar, and quartz. Advanced ceramics are made from synthetic materials, such as alumina, zirconia, and silicon carbide.Traditional ceramics are typically used in low-temperature applications, such as pottery, tiles, and bricks. Advanced ceramics are typically used in high-temperature applications, such as aerospace components and cutting tools.Ceramics have a number of unique properties that make them useful for a wide variety of applications. These properties include:Hardness and strength.Brittleness and low toughness.High melting point.Resistance to heat and chemicals.Electrical and thermal insulation.Low coefficient of thermal expansion.Chemical inertness.Ceramics are used in a wide variety of applications, including:Pottery and tableware.Tiles for floors and walls.Bricks for building construction.Refractories for lining furnaces and kilns.Aerospace components.Cutting tools.Medical devices.Electrical insulators.Thermal barriers.Ceramics are a versatile and important class of materials that have a wide range of applications. They are used in everything from everyday household items to high-tech aerospace components.中文回答:陶瓷。

介绍航材的书籍

介绍航材的书籍

介绍航材的书籍以下是一些关于航空材料的书籍推荐:1.《航空材料学导论》(Introduction to Aerospace Materials) - 作者:Admiralty这本书是航空材料学的经典教材,涵盖了航空材料的性能、制备、失效、使用和性能提高等方面的内容。

2.《航空航天材料、工艺与应用》(Aerospace Materials, Processes and Applications) - 作者:Brian Cantor、Patrick Grant等该书是一本全面介绍航空航天领域材料和工艺的教材,涵盖了航空航天材料的种类、特性、应用等方面的内容。

3.《航空材料和工艺》(Aerospace Materials and Processes) - 作者:George Titterton本书对航空材料的性能和使用进行了详细介绍,并重点关注了航空材料的加工和制备工艺。

4.《航空材料与工艺》(Aircraft Materials and Processes) - 作者:George F. Titterton该书全面地介绍了航空材料的种类、特性、加工和应用等内容,特别关注了航空工业中的材料选用和工艺技术。

5.《航空航天材料与制造技术》(Aerospace Materials and Manufacturing Technologies) - 作者:Victor A. Anderle、Rose L. Aggarwal等这本书以航空航天材料和制造技术为中心,讲述了航空航天材料的种类、性能和应用,同时介绍了制造航空航天零部件的工艺。

这些书籍在航空航天材料领域具有一定的权威性和专业性,能够为读者提供全面的航材知识和相关技术。

无论是对航空航天专业学生还是从业人员都是有价值的参考工具。

SAE AMS 2759-7B-2010

SAE AMS 2759-7B-2010

__________________________________________________________________________________________________________________________________________ SAE Technical Standards Board Rules provide that: “This report is published by SAE to advance the state of technical and engineering sciences. The use of this report is entirely voluntary, and its applicability and suitability for any particular use, including any patent infringement arising therefrom, is the sole responsibility of the user.”SAE reviews each technical report at least every five years at which time it may be reaffirmed, revised, or cancelled. SAE invites your written comments and suggestions. Copyright © 2010 SAE InternationalAll rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted, in any form or by any means, electronic, mechanical,photocopying, recording, or otherwise, without the prior written permission of SAE.TO PLACE A DOCUMENT ORDER: Tel: 877-606-7323 (inside USA and Canada)Tel: +1 724-776-4970 (outside USA)Fax: 724-776-0790Email: CustomerService@SAE WEB ADDRESS: AMS2759/7Issued 1991-10RATIONALEAMS2759/7B is an update of this specification to include Low Pressure Vacuum Carburizing (LPC) and positive pressure gas quenching, (PPGQ), typically referred to as high pressure gas quenching, (HPGQ).1. SCOPEThis specification, in conjunction with the general requirements for steel heat treatment covered in AMS2759, establishes the requirements and procedures for three classes of gas, vacuum, liquid, and low pressure (LPC) carburizing and related heat treatment of parts fabricated from carburizing grade steels. It does not cover pack carburizing.1.1 ClassificationParts to be carburized shall be processed to meet the requirements of one of the following classes:Class 1: Case depth and case hardness shall be as specified. Subsurface case hardness shall be in accordance with Table 1. Surface carbon shall be 0.70 to 1.00% (weight %). Retained austenite shall not exceed 10%.Intergranular carbides shall be scattered and discontinuous and shall not be evident in more than 40% of thegrain boundaries.Class 2: Case depth and case hardness shall be as specified. Subsurface case hardness shall be in accordance with Table 1. Surface carbon shall be 0.75 to 1.10% (weight %). Retained austenite shall not exceed 20%.Continuous carbide network shall not be evident in more than 80% of the grain boundaries.Class 3: Case depth and case hardness shall be as specified.1.1.1 If class is not specified, parts shall be processed to meet the requirements of Class2.1.2 TypesType 1: Gas and vacuum carburizingType 2: Liquid (salt bath) carburizingType 3: Low Pressure (vacuum) carburizing (0.5 to 35 mbar)1.2.1 If the type is not specified, Type 1 shall be used.1.3 Safety - Hazardous Materials While the materials, methods, applications, and processes described or referenced in this specification may involve theuse of hazardous materials, this specification does not address the hazards that may be involved in such use. It is the sole responsibility of the user to ensure familiarity with the safe and proper use of any hazardous materials and to take necessary precautionary measures to ensure the health and safety of all personnel involved.2. APPL ICABLE DOCUMENTSThe issue of the following documents in effect on the date of the purchase order forms a part of this specification to the extent specified herein. The supplier may work to a subsequent revision of a document unless a specific document issue is specified. When the referenced document has been cancelled and no superseding document has been specified, the last published issue of that document shall apply.2.1 SAE PublicationsAvailable from SAE International, 400 Commonwealth Drive, Warrendale, PA 15096-0001, Tel: 877-606-7323 (inside USA and Canada) or 724-776-4970 (outside USA), .AMS2418 Plating, CopperAMS2750 PyrometryAMS2759 Heat Treatment of Steel Parts, General RequirementsAMS2759/1 Heat Treatment of Carbon and Low-Alloy Steel Parts Minimum Tensile Strength Below 220 ksi(1517 MPa)AMS2759/2 Heat Treatment of Low-Alloy Steel Parts Minimum Tensile Strength 220 ksi (1517 MPa) andHigherAMS2759/11 Stress Relief of Steel PartsAMS2769 Heat Treatment of Parts in Vacuum ARP1820Chord Method of Evaluating Surface Microstructural Characteristics J423 Methods of Measuring Case Depth2.2 ASTM PublicationsAvailable from ASTM I nternational, 100 Barr Harbor Drive, P.O. Box C700, West Conshohocken, PA 19428-2959, Tel: 610-832-9585, .ASTM E 3Preparation of Metallographic Specimens ASTM E 18Rockwell Hardness and Rockwell Superficial Hardness of Metallic Materials ASTM E 384Microindentation Hardness of Materials ASTM E 415Optical Emission Vacuum Spectrometric Analysis of Carbon and Low Alloy Steel ASTM E 1019 Determination of Carbon, Sulfur, Nitrogen, Oxygen, and Hydrogen in Steel and in I ron, Nickel,and Cobalt Alloys2.3 ASM PublicationsAvailable from ASM I nternational, 9639 Kinsman Road, Materials Park, OH 44073-0002, Tel: 440-338-5151, .ASM Handbook Volume 09 – Metallography and Microstructures (1985 Edition), ISBN 10: 0-87170-015-83. TECHNI CAL REQUIREMENTS3.1 EquipmentShall conform to the requirements of AMS2759.3.1.1 QuenchingEquipmentShall be in accordance with AMS2759 and AMS2769 section on inert gas quenching.3.1.2 AuxiliaryEquipmentShall be in accordance with AMS2759.3.1.3 Thermal Processing EquipmentPyrometry shall conform to AMS2750.3.1.4 CleaningEquipmentShall be in accordance with AMS2759.3.1.5 CarburizingEquipmentThe carburizing atmosphere shall be generated with mixtures of hydrocarbon compounds and gases reacting to supply the carbon. Circulation of the atmosphere shall be sufficient to provide uniform carburizing.3.1.5.1 For Classes 1 and 2 gaseous carburizing, the process (time, temperature, gas flows (Type 1 vacuum only),carbon potential,) shall be automatically controlled, maintained and recorded. Manual equipment may be used to verify the automatic equipment.3.1.5.2 For Types 1 and 3 vacuum carburizing, precision gas flow meters (±3.5%) or mass flow sensors shall record theadditions of carburizing medium. The process (time, temperature, gas flows, vacuum levels, pressure, etc.) shall be automatically controlled, maintained and recorded. The carbon potential shall be determined by correlation of the additions with the results from carbon gradient test specimens.3.1.5.3 Other carburizing media, such as molten salt bath or fluidized beds, may be used when appropriate, exceptpack carburizing shall not be used. The carbon potential shall be determined by correlation with the results from carbon gradient test specimens. When molten salt baths are used, the medium shall be analyzed periodically for chemical composition.3.1.5.4 Carbon potential shall be determined in accordance with 3.11.8 for Type 1 gas carburizing.3.1.5.5 Accuracy of Atmosphere Control InstrumentsThe accuracy of instruments used for measuring and controlling carbon potential of Type 1 gas carburizing furnace atmospheres and the accuracy of instruments used for measuring and controlling pressure of Type 1 vacuum carburizing and Type 3 Low Pressure carburizing furnaces shall be checked as often as necessary to ensure that the equipment is operating properly and shall be calibrated. These activities shall be performed per manufacturers' recommendations.3.2 Sequence of OperationsShall be (1) preparation for carburizing, (2) carburizing, (3) cooling after carburizing, (4) hardening, and (5) tempering. The hardening operation may be omitted when cooling after carburizing has incorporated a quench in accordance with3.6.4, and when the conditions of 3.2.1, 3.2.2, or 3.2.3 are satisfied.--```,,`,,`,,`,3.2.1Parts were quenched from the carburizing temperature and both of the following apply: 3.2.1.1Case depth is 0.020 inch (0.51 mm) or less. 3.2.1.2 Carburizing temperature was not higher than 1600 °F (871 °C). 3.2.2 Parts were furnace cooled to the austenitizing temperature, stabilized, and quenched in accordance with 3.6.4and either of the following apply:3.2.2.1Parts were made from a low hardenability steel (e.g., 1020, 4615, 4620, 8615, or 8620). 3.2.2.2 Parts were made from a high hardenability steel (e.g., 4320, 4820, or 9310), and were carburized to meet Class3 requirements, or parts made to meet Class 1 or 2 requirements that have been approved by the cognizant engineering organization.3.2.3 Parts made from a low hardenability steel were quenched from the carburizing temperature and either of thefollowing applies:3.2.3.1Parts were carburized to meet Class 2 or Class 3 requirements. 3.2.3.2Parts were carburized to meet Class 1 requirements and quenching from the carburizing temperature was approved by the cognizant engineering organization. 3.3 Preparation for CarburizingAll metallurgical operations, such as brazing or welding, or stress inducing operations, such as forming or bending, should be completed prior to carburizing. Parts shall be free from visible defects, contamination, and corrosion that may retard carburizing or be detrimental to the appearance or performance of the finished parts.3.3.1 Stress Relief/NormalizingParts may be stress relieved per AMS2759/11 or normalized prior to carburizing. Normalizing times and temperatures for commonly carburized steels are given in Tables 2 and 3.3.3.2 CleaningAll parts shall have scale, oxides, residual oil film, and any other surface contamination removed prior to carburizing or heat treatment. Parts shall be cleaned as necessary for the process to be performed. Cautionary note: Pre-oxidation following washing has proven useful in Type 3 processing providing the temperature does not exceed 500 °F (260 °C)3.3.3 MaskingMasking shall be copper plate, not less than 0.0008 inches (20 μm) in thickness, applied in accordance with AMS2418. Other masking may be used if acceptable to the cognizant engineering organization.3.3.4 Visual I nspectionMasked or plated parts shall be visually inspected prior to and after carburizing. Parts exhibiting blistering, peeling, or porosity in the masking after carburizing shall be rejected.3.3.5 Loading of PartsLoad parts to minimize distortion at temperature and assure free circulation of atmosphere and quench fluid.--```,,`,,`,,`,,,````,``,,``,-`-`,,`,,`,`,,`---3.4 CarburizationTemperature3.4.1 CarburizingShall be at a selected temperature ±25 °F (±14 °C) consistent with the material to be carburized and the depth of case required. Carburizing ranges are as follows:Type 1 - Gas Carburizing: 1450 to 1750 °F (788 to 954 °C)Type 1 - Vacuum Carburizing:1550 to 1900 °F (843 to 1038 °C)Type 2 - Liquid Carburizing: 1500 to 1750 °F (815 to 954 °C)Type 3 – Low Pressure Carburizing: 1450 to 2100 °F (788 to 1149 °C)Potential3.4.2 CarburizingThe carbon potential, however controlled, shall be such as to provide the required case carbon content and case depth.3.4.2.1 For Types 1 and 3 vacuum carburizing, the carbon potential shall be determined by correlation of the additionswith the results from carbon gradient test specimens. Cautionary note: Consideration must be given to the production operating conditions when developing a qualification/periodic testing plan for multiple chamber furnaces when evaluating carbon potential. Cautionary note: The surface area needs to be taken into consideration when establishing process control parameters.Carburizing3.5 Cooling afterShall be in accordance with one of the following:3.5.1 Quenching from the Carburizing Temperature3.5.1.1 Cooling in a protective atmosphere or vacuum to 900 °F (482 °C) or lower, followed by cooling at a rate notfaster than that provided by fan circulated air or atmosphere. Fan cooling from the carburizing temperature is permitted.3.5.1.2 Furnace cooling from the carburizing temperature to the austenitizing temperature in Table 2, stabilizing, andquenching, including press quenching. The press quenching procedure will require cognizant engineering approval.3.6 HardeningShall consist of austenitizing and quenching. It may be preceded by subcritical annealing in accordance with Tables 2 and 3, and cooling to ambient temperature.3.6.1 AtmosphereProtective atmosphere or masking or both shall be used to protect part surfaces from decarburization, carburization, intergranular oxidation, and other surface damage during sub- critical annealing or austenitizing. Parts exhibiting blistering or peeling of the masking in the prior masked areas after exposure to elevated temperature shall be subject to rejection.3.6.2 Rate of HeatingHard parts (>35 HRC) shall be preheated or stress relieved in accordance with AMS2929/11 prior to hardening. Preheating in air is permitted.--```,,`,,`,,`,,,````,``,,``,-`-`,,`,,`,`,,`---3.6.3 AustenitizingTemperature shall be as specified in Table 2. For steels not listed in Table 2, austenitizing temperatures shall be specified by purchaser. The charge shall be held within the specified temperature range for sufficient time for necessary diffusion and transformation to take place. The soak times shown in Table 3 are recommended times. Soaking time shall commence when all control, thermocouple(s) reach a temperature 5 °F (3 °C) below the austenitizing temperature or, and when the last of any other monitoring and recording thermocouples (excluding load thermocouples and thermocouples used only to monitor over-temperature) reach the minimum of the required temperature range. When soaking time is based on one or more load thermocouples, it shall start when all load thermocouples have reached the minimum of the required temperature range.. The proper time interval will vary with the type of steel, power input to furnace and size of charge, as well as the nominal thickness and configuration of the individual parts.3.6.4 QuenchingFollowing austenitizing, parts shall be quenched in the media specified in Table 2 and as follows:Quenching3.6.4.1 OilType 1 – Gas Carburizing: Quench in circulating oil at a temperature between 60 to 160 °F (16 to 71 °C) at the start of the quenching operation. The circulation of the oil shall be controlled so that the oil temperature does not exceed 200 °F (93 °C) at any time during the quenching operation. Parts may be quenched in a die or in an open basket, but in either case, the oil shall circulate around every part.Type 1 and Type 3 – Vacuum and Low Pressure Carburizing: Oil Quenching shall be performed by transferring the parts from a heating chamber to a separate chamber that has been backfilled with an inert gas or under vacuum/partial pressure and immersing the parts in circulating oil. Quench oil shall be compatible with the vacuum level used during initial evacuation/transfer and shall be capable of quenching the parts at a rate sufficient to meet specified property requirements. The oil temperature should be consistent with the manufactures recommendation.3.6.4.2 Molten salt or synthetic quenchants are permitted.3.6.4.3 MarquenchingParts shall be marquenched in a nitrate salt bath, oil bath, or alternate quenchant operated between 300 to 450 °F (149 to 232 °C). The parts shall be in the marquenching bath only for sufficient time to stabilize the parts at the bath temperature, but not less than two minutes, followed by cooling in still air.3.6.4.4 Positive Pressure Gas Quenching (PPGQ, > 1 bar)When gas quenching is specified, it shall be accomplished by transferring the parts from a heating chamber to a separate chamber or backfilling the heating chamber with a gas that has no detrimental metallurgical effect on the material being processed or on the furnace equipment. The system and the pressure of the backfilling gas selected shall be capable of cooling the parts at a rate sufficient to meet the material property requirements specified. The use of hydrogen as a quenching gas must be approved by the cognizant engineering organization.3.6.4.5 For steels other than those listed in Table 2, quench media shall be as specified by the purchaser.Treatment3.6.5 Sub-ZeroSub-zero treatment is required for parts carburized to Class 1 and Class 2 requirements and for steels containing 2.5% (total) or more of alloying elements when carburized to Class 3 requirements. Other parts shall be sub-zero treated when specified. Parts shall be held at -100 °F (-73 °C) or lower, for 1 hour per inch (25 mm) of thickness, but not less than 1 hour, and warmed in air to room temperature. The sub-zero treatment shall be initiated within 2 to 4 hours after start of quench or completion of a snap temper. Parts less than 2.5 inches thick shall follow the 2 hour time and parts 2.5 inches and thicker shall meet the 4 hour time.3.6.5.1 When authorized by the cognizant engineering organization, a snap temper between 250 and 300 °F (121 and149 °C) may be used after quenching and prior to the sub-zero treatment when part design and thermal stresses may result in part cracking. The snap temper treatment shall be initiated within 2 hours after start of quench.3.6.6 CleaningParts may be cleaned before tempering. Marquenching salts shall be removed, before tempering in air, by a hot water rinse.3.7 TemperingTempering shall be started within 2 hours after start of quench or sub-zero treatment except as permitted in 3.7.1.3.7.1 I f hardened parts cannot be tempered within 2 hours after removal from sub-zero cooling, they shall be snaptempered for not less than 2 hours at a temperature between 250 °F and 300 °F (121 °C and 149 °C).3.7.2 Unless otherwise specified, parts shall be tempered for not less than 2 hours at a temperature consistent with thecase hardness requirements but within the range of 275 to 475 °F (135 to 246 °C). Soak time shall be per AMS2759/1 or AMS2759/2.3.8 Cleaning Carburized SurfacesShall be by one of the following methods; blast cleaning, detergent cleaning, vapor blast cleaning, degreasing, abrasive honing, or anodic electrolytic cleaning. Acid pickling or cathodic electrolytic cleaning is not permitted.Masking3.9 Removal ofMasking shall be removed from parts after the carburizing operation. If plating is used, it shall be removed by a method that is controlled to prevent etching, pitting or hydrogen embrittlement of the part.3.10 StraighteningStraightening carburized areas of parts is permitted only if done prior to sub-zero treatment and/or tempering and if approved by the cognizant engineering organization.3.10.1 Warm straightening is permitted in uncarburized areas of the parts. Part temperature shall not exceed 275 °F(135 °C) during the straightening operation.3.11 Properties3.11.1 Case Depth3.11.1.1 Case Depth MeasurementShall be determined in accordance with 3.11.1.1.1, 3.11.1.1.2, or 3.11.1.1.3.3.11.1.1.1 Case Depth Determination by Microhardness MethodShall be by microhardness traverse of a test specimen sectioned perpendicular to the carburized surface and prepared in accordance with ASTM E 3. Hardness shall be determined in accordance with ASTM E 384 or SAE J423, starting 0.002 inch (0.05 mm) from the carburized edge and traversing inward in increments of 0.004 inch (0.10 mm) to the depth where a hardness of 542 HK500 or 513 HV500 or less is reached. The case depth shall be the distance from the surface to the location where the hardness is equivalent to 50 HRC.--```,,`,,`,,`,,,````,``,,``,-`-`,,`,,`,`,,`---3.11.1.1.2 Case Depth Determination by Metallographic MethodShall be by examination of a test specimen sectioned perpendicular to the carburized surface and prepared in accordance with ASTM E 3. Etch the sectioned surface with a suitable reagent to get maximum contrast between phases and constituents, then examine at 40X to 60X magnification. The case depth shall be the distance from the surface to the location where the contrast is greatest. In case of dispute, the method of 3.11.1.1.1 shall apply.3.11.1.1.3 The method of ARP1820 may be used to determine depth of thin cases.3.11.1.2 Case Depth Requirements and Allowances3.11.1.2.1 The depth of the applied case on the as-carburized and hardened part shall be sufficient to assure thatengineering drawing required finished case depth and surface hardness requirements are met. The casedepth is defined as the depth below the surface of the finished part where the hardness is the equivalent of 50HRC. (See also 3.11.3.) This is often referred to as the “effective case depth”.3.11.1.2.2 The drawing case depth applies to the finish machined surfaces. The effective case depth at externalcorners, internal corners, boundaries, internal bores and gears and splines shall be as follows:3.11.1.2.2.1 For external edges with a radius less than two times the maximum specified case depth, the case depthmay be exceeded for a distance from the corner equal to three times the minimum specified case depth.3.11.1.2.2.2 For internal corners with a radius less than two times the maximum specified case depth, the case depthmay be less than the minimum specified for a distance from the theoretical corner equal to two times theminimum specified case depth but not less than one half of the minimum specified case depth.3.11.1.2.2.3 For boundaries between carburized and uncarburized areas, the case depth may be less than the minimumspecified case depth for a distance from the boundary equal to two times the minimum specified case depthbut not less than one half the minimum specified case depth at the boundary. The carburized case mayextend by normal diffusion beyond the boundary by not more than twice the minimum specified case depth.3.11.1.2.2.4 For gears and splines, the specified case depth applies to the tooth surface at the pitch diameter. Casedepth at the root radius shall be not less than 0.75 times the minimum specified case depth.3.11.1.2.2.5 For internal bores, the case depth is applicable at the entrance and midpoint depth of bores open at bothends, and at the entrance and closed end of bores open at only one end.3.11.2 Case Surface HardnessShall be determined in accordance with 3.11.2.2.3.11.2.1 The roots of splines or gear teeth may exhibit a hardness not more than 2 HRC or equivalent numbers lowerthan that required at the pitch line. When approved by the cognizant engineering organization, a reduction of4 HRC or equivalent is acceptable.3.11.2.1.1 If a suitable surface is not accessible for hardness testing, the hardness at 0.002 inch (0.05 mm) obtained as --```,,`,,`,,`,,,````,``,,``,-`-`,,`,,`,`,,`---in 3.11.1.1 shall be the case hardness.3.11.2.2 Case Hardness DeterminationShall be in accordance with ASTM E 18 on the carburized and hardened surface, of the finished part using a superficial hardness test appropriate for the depth of case specified.3.11.3 Sub-Surface Case HardnessFor parts carburized to Class 1 and Class 2 requirements, the subsurface hardness shall meet the requirements of Table 1, determined in accordance with 3.11.3.2. Where a different hardness is specified, the subsurface hardness shall be as specified, when applicable.3.11.3.1 Sub-surface hardness requirements do not apply to roots of splines or gear teeth.3.11.3.2 Sub-surface Case Hardness DeterminationThe hardness traverse or 3.11.1.1 shall be used to determine the sub-surface case hardness. The microhardness conversion for 58 HRC shall be 690 HK500 or 653 HV500 and for 60 HRC shall be 732 HK500 or 697 HV500.3.11.4 Core HardnessShall be as specified, determined in accordance with 3.11.4.1.3.11.4.1 Core hardness shall be determined in accordance with ASTM E 18 on a noncarburized surface of the part, or ata location not less than five times the case depth from the surface, or at the approximate center of themicrostructure specimen (See 3.11.6.6). As an alternate method the core hardness can be established in accordance with ASTM E 384 at a location not less than five times the case depth from the surface.3.11.5 The hardness of non-carburized surfaces shall be in accordance with specified core hardness.3.11.6 Case MicrostructureShall be predominantly tempered martensite, determined in accordance with 3.11.6.6.3.11.6.1 Intergranular oxidation shall not exceed 0.0005 inch (0.013 mm) in depth from the unmachined surface.3.11.6.2 For Class 1 parts, any intergranular carbides on a finish machined working surface shall be scattered anddiscontinuous and shall not be evident in more than 40% of the grain boundaries. Only dispersed intergranular spheroidal (secondary) carbides are permitted more than two grains below the finish machined working surface.Massive or blocky carbides are unacceptable.3.11.6.3 For Class 2 parts, a continuous carbide network shall not be evident in more than 80% of the grain boundaries.Photomicrograph 13 on page 220 of ASM Handbook, Volume 09, 1985 Edition, is an illustration of the maximum acceptable continuous carbide microstructure. Photomicrographs 12 and 14 on page 220 of ASM Handbook, Volume 09, 1985 Edition, are illustrations of non-acceptable microstructures containing excessive carbides around the grain boundaries and massive carbides.3.11.6.4 The microstructure of a finished Class 1 part shall not show evidence of retained austenite in excess of Figure16 on page 220 of ASM Handbook, Volume 09, 1985 Edition. f interpretation of the microstructure isquestionable, or if it appears to represent retained austenite in excess of this figure, x-ray diffraction shall be performed to determine the acceptability. When inspected by x-ray diffraction, retained austenite greater than 10% is unacceptable.3.11.6.5 The microstructure of a finished Class 2 part shall not show evidence of retained austenite in excess of Figure17 on page 221 of ASM Handbook, Volume 09, 1985 Edition. f interpretation of the microstructure isquestionable, or if it appears to represent retained austenite in excess of this figure, x-ray diffraction shall be performed to determine the acceptability. When inspected by x-ray diffraction, retained austenite greater than 20% is unacceptable.3.11.6.6 Case Microstructure DeterminationShall be by examination of a test specimen sectioned perpendicular to the carburized surface and prepared in accordance with ASTM E 3. Examine at 900X to 1100X magnification for retained austenite, 400X to 600X for intergranular oxidation and carbides, and 200X to 300X for core structure. For part surfaces that are to be subsequently machined, the stock to be removed in finish machining need not be evaluated.3.11.7 Core MicrostructureThe transformed microstructure of the core shall be consistent with the steel composition and the thickness of the part at the time of quenching.3.11.8 Carbon Content of Case (Carbon Potential or surface carbon)Shall be 0.70 to 1.00% for parts carburized to Class 1 requirements and 0.75 to 1.10% for parts carburized to Class 2 requirements, determined in accordance with 3.11.8.1, 3.11.8.2, or 3.11.8.33.11.8.1 A machined specimen, not less than 0.50 inch (12.7 mm) in diameter and 6 inches (152 mm) in length shall becarburized, preferably with a furnace load, for each alloy processed. The specimen shall be carburized to a depth not less than the maximum depth normally carburized or 0.020 inch (0.51 mm), whichever is greater.The specimen shall not be hardened after carburizing. 0.005 inch (0.13 mm) shall be machined from the diameter of the carburized specimen and the chips discarded. Chips for analysis shall be taken from the next0.005 inch (0.13 mm) machined from the diameter. The chips shall be free of oil, grease, dirt, scale, or otherforeign substances. Carbon determination may be by any method acceptable to purchaser, but in case of dispute, the combustion analysis method of ASTM E 1019 shall govern.3.11.8.2 A second method requires a specimen, not thicker than 0.01 inch (0.25 mm), of the same material as isrequired to be carburized, may be tested. I n this case, the entire thickness of the specimen is analyzed for carbon content using the combustion analysis method of ASTM E 1019.3.11.8.3 A final alternative method requires a specimen, not less than 0.5 inches (12.5 mm) thick of the same materialas is to be carburized, to be tested using Optical Emission Spectroscopy (OES) to ASTM E 415 or similar methods acceptable to the purchaser.4. QUALITY ASSURANCE PROVISIONS4.1 Responsibility for InspectionShall be in accordance with AMS2759. Where test specimens are required, except for specimens for case carbon determination, these shall be supplied by purchaser.4.2 Classification of TestsTests4.2.1 AcceptanceTests for case depth (3.11.1), case surface hardness (3.11.2), sub-surface case hardness (3.11.3), core hardness (3.11.4), hardness of noncarburized surfaces (3.11.5), case microstructure (3.11.6), and core microstructure (3.11.7) are acceptance tests and shall be performed on each lot.Tests4.2.2 PeriodicTests for carbon content of the case (3.11.8) are periodic tests and shall be performed every six months unless frequency of testing is specified by purchaser.。

SAE AMS-C-5541A-2003 铝和铝合金的化学转化膜

SAE AMS-C-5541A-2003    铝和铝合金的化学转化膜

SAE Technical Standards Board Rules provide that: “This report is published by SAE to advance the state of technical and engineering sciences. The use of this report is entirely voluntary, and its applicability and suitability for any particular use, including any patent infringement arising therefrom, is the sole responsibility of the user.”SAE reviews each technical report at least every five years at which time it may be reaffirmed, revised, or cancelled. SAE invites your written comments and suggestions.Copyright © 2003 SAE InternationalAll rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted, in any form or by any means, electronic, mechanical, photocopying,recording, or otherwise, without the prior written permission of SAE.TO PLACE A DOCUMENT ORDER:Tel: 877-606-7323 (inside USA and Canada)Tel: 724-776-4970 (outside USA)Chemical Conversion Coatings on Aluminum and Aluminum AlloysAREA MFFP CANCELLATION NOTICEThis specification has been declared “CANCELLED” by the Aerospace Materials Division, SAE, as of July, 2003, and has been superseded by MIL-C-5541. The requirements of the latest issue of MIL-C-5541 shall be fulfilled whenever reference is made to the cancelled AMS-C-5541. By this action, this document will remain listed in the Numerical Section of the index of Aerospace Materials Specifications noting that it is superseded by MIL-C-5541. Cancelled specifications are available from SAE upon request.AEROSPACEMATERIALSPECIFICATION AMS-C-5541A IssuedJUN 1999Cancelled JUL 2003Superseding AMS-C-5541--``,,``,`````,```,,,`,```,,,``-`-`,,`,,`,`,,`---NOTICEThis document has been taken directly from U.S. Military Specification MIL-C-5541E and contains only minor editorial and format changes required to bring it into conformance with the publishing requirements of SAE technical standards. The initial release of this document is intended to replace MIL-C-5541E. Any part numbers established by the original specification remain unchanged.The original Military Specification was adopted as an SAE standard under the provisions of the SAE Technical Standards Board (TSB) Rules and Regulations (TSB 001) pertaining to accelerated adoption of government specifications and standards. TSB rules provide for (a) the publication of portions of --``,,``,`````,```,,,`,```,,,``-`-`,,`,,`,`,,`---unrevised government specifications and standards without consensus voting at the SAE Committee level, and (b) the use of the existing government specification or standard format.Under Department of Defense policies and procedures, any qualification requirements and associated qualified products lists are mandatory for DOD contracts. Any requirement relating to qualified products lists (QPL’s) has not been adopted by SAE and is not part of this SAE technical document.1.SCOPE:1.1Scope:This specification covers the requirements for two classes of chemical conversion coatings formed by the reaction of chemical conversion materials and the surfaces of aluminum and aluminum alloys.This specification is intended specifically to provide components of military weapon systems with maximum corrosion resistance. The coating also provides a surface having better paint adhesion than uncoated aluminum. It is not intended as a general purpose coating for commercial anddecorative applications, (see 6.1).1.2Classification:The chemical conversion coatings shall be of the following classes, as specified (see 6.2).1.2.1Classes:Class 1 A - For maximum protection against corrosion, for surfaces to be painted or left unpainted, (see 6.1.1).Class 3 - For protection against corrosion where lower electrical resistance is required, (see 6.1.2).2.APPLICABLE DOCUMENTS:The following publications, of the issue in effect on date of invitation for bids or request for proposal, form a part of this specification to the extent specified herein.2.1U.S. Government Publications:Available from DODSSP, Subscription Services Desk, Building 4D, 700 Robbins Avenue,Philadelphia, PA 19111-5094.QQ-A-250/4Aluminum Alloy 2024, Plate and SheetQQ-A-250/11Aluminum Alloy 6061, Plate and SheetMIL-P-23377Primer Coating, Epoxy Polyamide, Chemical and Solvent ResistantMIL-C-81706Chemical Conversion Materials For Coating Aluminum and Aluminum AlloysMIL-P-85582Primer Coatings: Epoxy, WaterborneFED-STD-141Paint, Varnish, Lacquer and Related Materials, Methods of Inspection, Sampling and TestingMIL-STD-105Sampling Procedures and Tables for Inspection by Attributes2.2ASTM Publications:Available from ASTM, 100 Barr Harbor Drive, West Conshohocken, PA 19428-2959.ASTM B 117Salt Spray (Fog) Testing2.3Order of precedence:In the event of a conflict between the text of this document and the references cited herein, the text of this document takes precedence. Nothing in this document, however, supersedes applicable lawsand regulations unless a specific exemption has been obtained.3.REQUIREMENTS:3.1Chemical conversion materials:The materials used to produce a chemical conversion coating shall be approved for the selected class, form and application method in accordance with the qualification requirements ofMIL-C-81706 and been accepted for listing on the applicable Qualified Products List (see 6.3).Replenishing chemicals, such as fluorides, added to a bath to maintain its efficiency, shall in no way degrade the performance of the coating being applied.3.2Cleaning:Prior to coating, the base metal shall be mechanically and/or chemically cleaned such that a water break-free surface is obtained after rinsing (see 6.4). Abrasives containing iron such as steel wool, iron oxide, rouge or steel wire are prohibited for all cleaning operations as particles from them may become embedded in the metal and accelerate corrosion of the aluminum and aluminum alloys.Treated parts which have become soiled shall be cleaned with materials which will remove the soil without damaging the base metal, the part, or the conversion coating. If the coating is damaged, the damaged area shall be recleaned and recoated or the part shall be rejected.3.3Application:Unless an application method is specified, the chemical conversion materials shall be appliednonelectrolytically by spray, brush or immersion after all heat treatments and mechanical operations such as forming, perforating, machining, brazing and welding have been completed. Assemblies containing non-aluminum parts which may be attacked, embrittled, or damaged in any way by the conversion coating process shall not be coated as assemblies unless the non-aluminum parts are suitably masked.--` ` , , ` ` , ` ` ` ` ` , ` ` ` , , , ` , ` ` ` , , , ` ` -` -` , , ` , , ` , ` , , ` ---3.4Rework:Unless otherwise specified by the procuring activity, mechanically damaged areas from which the coating has been removed may be reworked. The damaged areas shall be touched up withMIL-C-81706 material approved on the QPL for the applicable class and method of application. The rework area shall not exceed 5 percent of total item surface area. If the area exceeds 5 percent, specific approval must be obtained from the procuring activity before the area can be reworked.3.5Appearance:The conversion coating shall be as uniform in appearance as practical (see 6.6). It shall becontinuous and free from areas of powdery or loose coating, voids, scratches, flaws and otherdefects or damages which will reduce the serviceability of parts or be detrimental to the protective value and paint bonding characteristics. The size and number of contact marks shall be at aminimum, consistent with good practice. If specified, contact marks shall be touched up withMIL-C-81706 material approved on the QPL for the applicable class and method of application to prevent localized corrosion. Clear (colorless) coating shall only be used when specifically authorized by the procuring activity, (see 6.2 and 6.6).3.6Corrosion resistance properties:At the end of 168 hours exposure to the 5 percent salt spray test specified in 4.5.1, specimen panels (see 4.3.3) treated with the applicable class of coating shall meet all of the following corrosionresistance requirements:a.No more than 5 isolated spots or pits (see 6.7), none larger than 0.031 inches in diameter, perspecimen panel. Areas within 0.25 inches from the edges, identification markings, and holding points during processing or salt spray exposure shall be excluded. Loss of color shall not because for rejection.b.No more than 15 isolated spots or pits, none larger than .031 inches in diameter, on thecombined surface area of all five specimen panels, subjected to the salt spray test.3.7Paint adhesion properties:When the production paint system or the paint system specified in 4.3.3.1.1 is applied to theapplicable specimen panels (see 4.3.3), no intercoat separation shall occur between the paintsystem and the conversion coating or between the conversion coating and the base metal when tested in accordance with 4.5.2, (see 6.10). If the conversion coated parts do not require painting for end use, the paint adhesion test may be omitted if specifically authorized by the procuring activity (see 6.2).--` ` , , ` ` , ` ` ` ` ` , ` ` ` , , , ` , ` ` ` , , , ` ` -` -` , , ` , , ` , ` , , ` ---3.8Electrical contact resistance of Class 3 coatings:If specified (see 6.2), electrical contact resistance testing shall be performed. The test method, frequency of testing, and required resistance values shall be specified by the procuring activity to suit the needs of a particular application.3.9Workmanship:The chemical coatings covered by this specification shall be produced by suitable treatments and processes to give uniformly coated products as specified herein.4.QUALITY ASSURANCE PROVISIONS:4.1Responsibility for inspection:Unless otherwise specified in the contract or purchase order, the contractor is responsible for the performance of all inspection requirements (examinations and tests) as specified herein. Except as otherwise specified in the contract or purchase order, the contractor may use his own or any other facilities suitable for the performance of the inspection requirements specified herein, unlessdisapproved by the Government. The Government reserves the right to perform any of theinspections set forth in the specification where such inspections are deemed necessary to ensure supplies and services conform to prescribed requirements.4.1.1Responsibility for compliance: All items must meet all requirements of Section 3. The inspectionset forth in this specification shall become a part of the contractor’s overall inspection system or quality program. The absence of any inspection requirements in the specification shall not relieve the contractor of the responsibility of ensuring that all products or supplies submitted to theGovernment for acceptance comply with all requirements of the contract. Sampling inspection, as part of manufacturing operations, is an acceptable practice to ascertain conformance torequirements, however, this does not authorize submission of known defective material, eitherindicated or actual, nor does it commit the Government to acceptance of defective material.4.2Classification of inspection:--``,,``,`````,```,,,`,```,,,``-`-`,,`,,`,`,,`---The inspection requirements specified herein are classified as follows:a.Process control inspection (see 4.3).b.Quality conformance inspection (see 4.4).4.3Process control inspection:4.3.1Process control tests and solution analysis: To assure continuous control of the process, testspecimens (see 4.3.3) shall be tested in accordance with Table I (see 4.3.1.1). In addition to the tests in Table I, solution analysis shall be performed on all the processing solutions in theconversion coating line (see 6.9) to verify that the chemical concentrations are within rangesestablished for optimum performance (see 4.3.1.1 and 4.3.2). Process control tests are conducted to determine compliance of the chemical conversion coatings with the requirements of thisspecification and are acceptable as evidence of the properties being obtained with the equipment and procedures employed.Table I. Process control tests.4.3.1.1Frequency of process control testing and solution analysis: Solution analysis shall be performedonce every week. The process control tests specified in Table I shall be conducted on a monthly basis. In addition, the interval between each monthly test shall not exceed 35 days. If production in accordance with this specification is not performed for a period of 35 days or longer, process control tests and solution analysis shall be conducted at the restart of production.4.3.2Solution analysis records: The processor shall maintain a record of the history of each processingbath, showing additions of replenishing chemicals to the bath and the results of all solutionanalyses performed. Upon request of the procuring activity, such records, as well as reports of the test results, shall be made available. These records shall be maintained for not less than one year after completion of the contract or purchase order.--` ` , , ` ` , ` ` ` ` ` , ` ` ` , , , ` , ` ` ` , , , ` ` -` -` , , ` , , ` , ` , , ` ---4.3.3Process control specimen panels: Specimen panels used for process control testing shall be3inches in width, 10 inches in length, with a minimum 0.020 inch nominal thickness. Thespecimen panels shall be processed with the hardware during an actual production run, including all pre- and post-treatment processes such as cleaning and rinsing, except as specified below.Unless otherwise specified in the contract or order (see 6.2), either of the following alloy options for the process control specimen panels may be utilized:Option 1 - A set of specimen panels shall be used for each alloy and temper treated during themonthly process control period.Option 2 - The specimen panels shall be 2024-T3 aluminum alloy panels per QQ-A-250/4 for class 1A coatings and 6061-T6 aluminum alloy panels per QQ-A-250/11 for class 3 coatings. If desired, 2024-T3 panels may be used in lieu of 6061-T6 panels for testing class 3 coatings (see 6.8). When castings are being processed and the cleaning procedures used are detrimental to the wrought --``,,``,`````,```,,,`,```,,,``-`-`,,`,,`,`,,`---specimen panels, the panels shall be cleaned in an appropriate manner (see 3.2) and conversion coated with the castings.4.3.3.1Preparation of paint adhesion specimens: Unless otherwise specified (see 6.2), the paint systemto be used on the specimen panels for adhesion testing (see 4.5.2) shall be that used for theproduction work (applied and cured in the same manner as the production work) or the paintsystem specified in 4.3.3.1.1.4.3.3.1.1Epoxy primer coatings: Specimen panels shall be finished with one coat of a (VOC) compliantepoxy-polyamide primer conforming to either MIL-P-23377 or MIL-P-85582. In either case theprimer shall be applied to a dry film thickness of 0.0006 to 0.0009 inch (0.6 to 0.9 mil) and driedin accordance with the applicable primer specification before testing in accordance with 4.5.2.4.3.4Failure: Failure to conform to any of the process control requirements specified in Table I shallresult in immediate halt of production. The reason for failure shall be determined and corrected before production resumes. All traceable and retrievable work from the time the failed processcontrol specimens were conversion coated to the time when the failure was determined shall be rejected, unless the contractor can demonstrate that the items under review can meet therequirements of this specification. Unless otherwise specified, parts which have been painted or incorporated into an assembly shall not be considered retrievable.4.4Quality conformance (lot acceptance) inspection:4.4.1Lot: A lot shall consist of all conversion coated items of the same class, treated under the sameconditions, and submitted for acceptance at one time. Unless otherwise specified, the lot size shall not exceed the number of parts, articles, items or components resulting from a one day’sproduction (see 6.2).4.4.2Sampling plan and acceptance criteria: Samples for visual examinations shall be selected fromeach lot of treated articles, items, parts or components. Unless otherwise specified in the contract or order (see 6.2), the sampling plan and acceptance criteria shall be as specified in inspection level II of MIL-STD-105 with an AQL of 1.5 percent defective.4.4.3Visual lot examination: Samples selected in accordance with 4.4.2 shall be visually inspected forcompliance with the requirements of 3.5 and 3.9.4.4.4Failure: Failure to conform to any of the quality conformance requirements shall result in rejectionof the represented lot.4.5Test methods:4.5.1Corrosion resistance test: Five specimen panels prepared in accordance with paragraph 4.3.3shall be used for corrosion resistance testing. After the coating application, the specimen panels shall be dried at 60-100°F for 24 hours. The panels shall then be subjected to a 5 percent saltspray test in accordance with ASTM B117 for 168 hours, except that the significant surface shall be inclined 6 degrees from the vertical. After exposure, test pieces shall be cleaned in running water, not warmer than 38°C (100°F), blown with clean, dry unheated air, and visually examined forconformance with paragraph 3.6.4.5.2Wet tape adhesion test: Two specimen panels prepared in accordance with 4.3.3 and 4.3.3.1 shall --``,,``,`````,```,,,`,```,,,``-`-`,,`,,`,`,,`---be tested for wet tape adhesion. The test shall be conducted as described in method 6301 ofFED-STD-141 to determine conformance with paragraph 3.7.5.PACKAGING:5.1The requirements of Section 5 are not applicable.6.NOTES:(This section contains information of a general or explanatory nature that may be helpful, but is not mandatory.)6.1Intended use:6.1.1Class 1A: Class 1A chemical conversion coatings are intended to provide corrosion preventionwhen left unpainted as well as to improve adhesion of paint finish systems on aluminum andaluminum alloys. Coatings of this type may be used, for example, on tanks, tubing, andcomponent structures where paint finishes are not required for the interior surfaces but arerequired for the exterior surfaces.6.1.2Class 3: Class 3 chemical conversion coatings are intended for use as a corrosion preventive filmfor electrical and electronic applications where lower resistant contacts, relative to Class 1Acoatings, and anodic coatings in accordance with MIL-A-8625, are required (see 6.1.2.1). Theprimary difference between a Class 1A and Class 3 coating is thickness, since current passesmore readily through a thinner current resistant barrier (coating). Coating thickness is varied by immersion time, and as a result, the same conversion material can be listed on QPL-81706 for both classes. Because Class 3 coatings are thinner, they are more susceptible to corrosion than Class 1A coatings. If it is required to paint areas surrounding electrical contacts, Class 3 coatings will improve adhesion of paint systems on aluminum and aluminum alloys.6.1.2.1Electrical resistance testing: When under a nominal electrode pressure of 200 psi, Class 3coatings are qualified per MIL-C-81706 to have a resistance no greater than 5,000 microhms per square inch as supplied and 10,000 microhms per square inch after 168 hours of salt sprayexposure. In addition to the coating or coating thickness (see 6.1.2), other variables heavilyinfluence resistance values when using the test method specified in MIL-C-81706 or other similar methods. The following two variables may have a greater effect on electrical resistance values than the conversion coating thickness.6.1.2.1.1Surface roughness of the specimen panel: Panels having rough surfaces will yield lowerresistance values when subjected to a contact electrode pressure due to coating fracture. Thisreasoning can also be applied to the contact electrode.6.1.2.1.2Flatness of the contact electrode: If an electrode with a given surface area is not flat, the actualcontact area will be lower than the theoretical value. Smaller contact area will result in a higherresistance value. The same reasoning can be applied to the specimen panel.6.2Ordering data:Acquisition documents should specify the following:a.Title, number and date of this specification.b.Class of coating (see 1.2.1).c.Method of application, if restricted (see 3.3).d.Clear coatings, if desired (see 3.5).--``,,``,`````,```,,,`,```,,,``-`-`,,`,,`,`,,`---e.Omit the paint adhesion test, if permitted (see 3.7)f.If electrical resistance testing is required for Class 3 coatings, (see 3.8 and 6.1.2).g.When electrical resistance testing is required, specify the required resistance values, frequencyof testing, and test method (see 3.8 and 6.1.2).h.Alloy and temper of the process control specimen panels, if different than that specified in 4.3.3.i.Paint finish system for treated parts, if applicable (see 4.3.3.1)j.Lot size, if different from that specified (see 4.4.1).k.Sampling plan, if different from that specified (see 4.4.2).6.3Interchangeability:The various products approved in accordance with MIL-C-81706 and listed on QPL-81706 willprovide equivalent coatings within each class insofar as performance of the chemical conversion coating is concerned to the provisions of the document, but are not interchangeable from a chemical standpoint; that is, different materials can not be mixed. The materials from one supplier shall not be mixed or used to strengthen an existing solution from another material supplier. As the chemical coating materials are proprietary products, the ingredients, processes, the method of application (spray, brush, or immersion), and the equipment required for application of coating may vary.Coating contractors and military activities should take this into account in acquisition, in the design of parts and the establishment of facilities. Detail drawing of parts requiring treatment in accordance with this specification should specify the Class 1A or 3 and any paint finishing systems required to meet the performance desired. If the coating class is not specified, Class 1A is recommended.6.4Cleaners:Use of a non-etch cleaner is preferred, particularly on wrought alloys. If an etch is used, caution should be taken to prevent pitting or intergranular attack. This is particularly important when using an alkaline etch because the aluminum tends to be more soluble than its alloying elements and existing intermetallics, such as copper, may be further exposed. As a result, alkaline etching should be avoided (particularly when cleaning assembled structures). If an alkaline etch is used, it should always be followed by an acid neutralization step.6.5Abrasion resistance:The abrasion resistance of chemical coatings is relatively low. Coatings are reasonably durable when subjected only to moderate handling, but are readily removed by severe wear or erosion.However, cold forming operations, when performed with care, can generally be performed on treated metals without appreciable damage to the coatings.6.6Visual appearance:--``,,``,`````,```,,,`,```,,,``-`-`,,`,,`,`,,`---The simplest way to evaluate a conversion coating is to observe color, uniformity of appearance, smoothness and adhesion to the base metal (see 3.5). Visual examination is performed to assure that proper cleaning and coating procedures were used such that a coating with sufficient protection exists over the entire part. Materials qualified under MIL-C-81706 produce coatings that range in color from clear to iridescent yellow or brown. It may be possible to develop acceptable color levels for a particular coating system by use of color chips. The following circumstances may exist which relate to color uniformity:6.6 (Continued):a.When several alloys are processed with the same conversion chemical, color may vary fromalloy to alloy.b.Due to the high level of impurities and oxidation on the surfaces of aluminum welds and castings,color may not be as uniform as that obtained by treating wrought alloys.c.Dark spots may result from dripping or rundown of the conversion chemicals when the parts arelifted out of the treatment tank. A small amount of spotting will not result in coating degradation but should be minimized by quickly rinsing the parts after treatment, and use of proper racking --``,,``,`````,```,,,`,```,,,``-`-`,,`,,`,`,,`---techniques.Visual examination will not reveal if the protective value of the coating has been impaired bycontamination or by overheating during drying. If a clear coating is required, inspection difficulties may arise because visual inspection does not reveal the presence of a coating. The existence of a coating can be verified by using a simple spot test specified in ASTM B 449.6.7Determination of a corrosion spot or pit:As a general rule, a corrosion spot or pit usually displays a characteristic tail or line (see 3.6).6.8Specimen panels (2024-T3):Due to high copper content, 2024-T3 aluminum alloy panels are more susceptible to salt sprayfailure than 6061-T6 aluminum alloy panels (see 4.3.3).6.9Chemical analysis of the conversion solution:As a minimum, chemical analysis of the conversion solution should consist of concentration, pH, and temperature evaluations to determine that the bath is within the ranges specified by the chemical manufacturer. It should be noted that many conversion materials do not react sufficiently withaluminum surfaces at low temperatures. Conversion coating parts in an unheated facility (ie. a hangar) during colder periods of the year would not be recommended.6.10Paint adhesion:Coated parts should be allowed to dry in accordance with the chemical manufacturer’srecommendation before they are subsequently painted or adhesion failures may occur. Whencoated parts are stored for extensive periods before painting, they should be cleaned in accordance with 3.2 to reactivate the surface by removing dust particles. Excessively thick coatings may result in paint adhesion problems (blistering) due to higher amounts of soluble material under the paint.6.10.1Paint compatibility: Compatibility problems between conversion coatings and certain ChemicalAgent Resistant Coatings (CARC) have been reported.6.11Temperature effects on corrosion protection:Unpainted conversion coatings will commence losing corrosion resistance properties if exposed to temperatures of 60°C (140°F) or above, during drying, subsequent fabrication, or service. Ingeneral, as temperature and exposure times increase, the corrosion protection of unpaintedconversion coated parts decreases. The reduction is believed to result from the coating dehydrating and the resulting insolubility of the chromates within the coating.6.12This paragraph was deleted as it did not pertain to the converted SAE document.6.13Subject term (key word) listing:AluminumAluminum AlloysChemical Conversion CoatingsChromate Conversion CoatingsPREPARED UNDER THE JURISDICTION OF AMS COMMITTEE “B”--``,,``,`````,```,,,`,```,,,``-`-`,,`,,`,`,,`---。

material

material

materialMaterial is a diverse and essential component in various industries and applications. It can refer to various substances, whether natural or synthetic, that provide the raw materials for manufacturing processes. From construction to manufacturing, materials play a crucial role in shaping our built environment and everyday products. This document will explore the significance of materials, their types, and their applications in different sectors.Firstly, materials are of immense importance in the construction industry. They serve as the foundation for creating structures that are safe, durable, and aesthetically pleasing. In this sector, materials such as concrete, steel, and wood are commonly used. Concrete is a versatile material that is used for building foundations, walls, and floors. It is favored for its strength and durability. Steel, on the other hand, is known for its high strength-to-weight ratio, making it suitable for constructing robust structures like bridges and skyscrapers. Wood is another common material used in construction, renowned for its versatility and natural beauty. It is used for framing, flooring, and finishing touches.In addition to construction, materials are fundamental in manufacturing industries. They are used to create anextensive range of products, from consumer goods to industrial machinery. Examples of materials used in manufacturing include metals, plastics, and ceramics. Metals are utilized for their excellent mechanical properties, electrical conductivity, and heat resistance. They are widely used in the production of automobiles, aircraft, and appliances. Plastics are valued for their versatility, lightweight nature, and resistance to corrosion. They are employed in the manufacturing of packaging materials, household items, and electronic devices. Ceramics, known for their high strength and thermal resistance, are used in the production of cutting tools, electrical insulators, and heat shields.Materials also have critical applications in the energy sector. Renewable energy sources such as solar, wind, and hydroelectric power require specific materials for their infrastructure. For example, solar panels rely on thin film materials such as silicon to convert sunlight into electricity. Wind turbines utilize advanced composite materials such as fiberglass and carbon fiber to withstand extreme weather conditions. Hydroelectric power plants use materials like concrete and steel for dam construction. Additionally, materials like lithium-ion batteries are crucial for energy storage in electric vehicles and portable electronic devices.Moreover, materials are indispensable in the medical field. They are widely used in medical equipment, implants, and prosthetics. For instance, titanium and stainless steel alloys are commonly used in the production of surgical instruments, dental implants, and joint replacements due to their biocompatibility and corrosion resistance. Plastics and polymers are utilized in various medical applications, including catheters, prosthetic limbs, and drug delivery systems, thanks to their high durability and design flexibility.Lastly, materials are essential in the aerospace industry. Aerospace materials must meet rigorous standards for weight reduction, strength, and resistance to high temperatures. Lightweight and strong materials like aluminum, titanium, and composites are used in aircraft manufacturing to enhance fuel efficiency and performance. Composite materials, composed of distinct components like carbon fiber and epoxy resin, are particularly favored for their high strength-to-weight ratio and resistance to fatigue.In conclusion, materials are a fundamental element in various industries and applications. Construction, manufacturing, energy, medical, and aerospace sectors all rely heavily on materials to create functional, safe, and innovative products and structures. The versatility and performance of materials have significantly contributed to technological advancementsand the improvement of our everyday lives. Therefore, the study and development of materials continue to be of great importance in several industries, as they drive progress and innovation in various fields.。

有关航天的材料作文英语

有关航天的材料作文英语

有关航天的材料作文英语Title: Advancements in Aerospace Materials。

In the vast expanse of the aerospace industry, materials play a pivotal role in shaping the trajectory of exploration and innovation. From the earliest days offlight to the cutting-edge technologies of today, the evolution of aerospace materials has been nothing short of remarkable. This essay delves into the fascinating realm of aerospace materials, exploring their significance, advancements, and future prospects.### Significance of Aerospace Materials。

Aerospace materials serve as the backbone of every aircraft and spacecraft, dictating their performance, durability, and safety. The demands placed upon these materials are immense—they must withstand extreme temperatures, pressures, and forces encountered during flight, all while remaining lightweight to maximize fuelefficiency. Consequently, the selection and development of aerospace materials are critical tasks that directly impact the success of missions and the safety of crew and passengers.### Advancements in Aerospace Materials。

aerospace的用法总结大全

aerospace的用法总结大全

aerospace的用法总结大全(学习版)编制人:__________________审核人:__________________审批人:__________________编制学校:__________________编制时间:____年____月____日序言下载提示:该文档是本店铺精心编制而成的,希望大家下载后,能够帮助大家解决实际问题。

文档下载后可定制修改,请根据实际需要进行调整和使用,谢谢!并且,本店铺为大家提供各种类型的经典范文,如英语单词、英语语法、英语听力、英语知识点、语文知识点、文言文、数学公式、数学知识点、作文大全、其他资料等等,想了解不同范文格式和写法,敬请关注!Download tips: This document is carefully compiled by this editor.I hope that after you download it, it can help you solve practical problems. The document can be customized and modified after downloading, please adjust and use it according to actual needs, thank you!In addition, this shop provides various types of classic sample essays, such as English words, English grammar, English listening, English knowledge points, Chinese knowledge points, classical Chinese, mathematical formulas, mathematics knowledge points, composition books, other materials, etc. Learn about the different formats and writing styles of sample essays, so stay tuned!aerospace的用法总结大全aerospace的意思aerospace的简明意思n. 宇宙空间;航空航天学;航空航天工业adj. 航天的;太空的英式发音 ['eərəʊspeɪs] 美式发音 ['eroʊspeɪs]aerospace的具体用法如:D laser cutting has been widely used in automobile and aerospace industry.三维激光切割在汽车、航空航天工业等领域得到越来越广泛的应用.在此句中aerospace表示航空航天工业的意思aerospace的用法例句Titanium alloys are widely used in aerospace industry due to their excellent mechanical properties.钛合金是航空航天工业中应用广泛的一种难加工材料.在此句中aerospace表示航空航天工业的意思France is also more than, say, Airbus, matches, and Aerospace Industries Association.法国的公司也多, 比如说空客, 赛风,航空航天工业协会.在此句中aerospace表示航空航天工业的意思Its applications in aerospace, industry and national defense fields are also briefly introduced.简要介绍了其在航空航天、工业及国防等领域的应用情况.在此句中aerospace表示航空航天工业的意思AIR FLEET is distributed through direct mail to all potential markets of the Russian aerospace industry.航空机队以直接邮寄的方式发行到俄罗斯航空航天工业的所有潜在市场.在此句中aerospace表示航空航天工业的意思the aerospace industry航空航天工业在此句中aerospace表示航空航天工业的意思。

有关航天的材料作文英语

有关航天的材料作文英语

有关航天的材料作文英语英文回答:Materials play a critical role in aerospace engineering, enabling the design and construction of spacecraft that can withstand the extreme conditions of space. These materials must be lightweight, strong, and resistant to high temperatures, radiation, and micrometeoroids.One of the most important materials used in aerospaceis aluminum. Aluminum alloys are lightweight and strong, making them ideal for use in aircraft structures. They are also resistant to corrosion and can be easily welded and formed. Carbon fiber composites are another important material used in aerospace. Carbon fiber composites are lightweight and extremely strong, making them suitable for use in high-performance aircraft and spacecraft. They are also resistant to heat and radiation.In addition to aluminum and carbon fiber composites, avariety of other materials are used in aerospace. These include titanium, steel, ceramics, and polymers. Each material has its own unique properties that make it suitable for specific applications. For example, titanium is used in high-temperature applications, while ceramics are used in applications where resistance to wear and tear is important.The selection of materials for aerospace applications is a critical decision that must be made carefully. The materials used must meet the specific requirements of the application, while also being cost-effective. By carefully selecting the right materials, aerospace engineers can design and build spacecraft that are safe, reliable, and efficient.中文回答:太空材料在航空航天工程中至关重要,它可以设计并制造能够承受太空极端条件的航天器。

复合材料英文文献

复合材料英文文献

复合材料英文文献Composite materials are engineered to combine the best properties of different materials, creating a new material that is stronger, lighter, and more durable than its individual components.These innovative materials are widely used in various industries, from aerospace where they reduce weight and increase fuel efficiency, to construction where they enhance structural integrity and longevity.The versatility of composite materials lies in their ability to be tailored to specific applications. By varying the composition and arrangement of the constituent materials, engineers can optimize the material for strength, stiffness, or resistance to environmental factors.Recent advancements in nanotechnology have further expanded the capabilities of composites. The incorporation of nanomaterials into composite structures can significantly improve their mechanical and thermal properties.One of the key challenges in composite material research is the development of effective recycling strategies. As these materials become more prevalent, finding sustainable ways to reuse or recycle them will be crucial to minimize environmental impact.Educational institutions and industries alike are investing in research to explore new composite material applications. This includes everything from improving sports equipment to developing next-generation energy storage systems.In conclusion, composite materials represent asignificant leap forward in material science. Their unique properties and potential for customization make them indispensable in a wide range of applications, driving innovation and enhancing performance across multiple sectors.。

ams6931标准 -回复

ams6931标准 -回复

ams6931标准-回复AMS 6931 Standard: A Complete Guide to Aerospace Material SpecificationsIntroductionAMS 6931 is a key standard in the aerospace industry and plays an essential role in ensuring the quality and reliability of materials used in aircraft manufacturing. In this article, we will delve into the details of AMS 6931 and provide a step-by-step explanation of its core components and their significance.Step 1: Understanding AMS 6931AMS 6931 is a material specification standard established by the Society of Automotive Engineers (SAE). It specifically pertains to the requirements for titanium and titanium alloy bars, forgings, and rings used in aerospace applications. This standard outlines the minimum mechanical properties, chemical composition, and testing procedures that these materials must meet to ensure their suitability for aerospace use.Step 2: Material IdentificationThe first aspect covered in AMS 6931 is the identification and labeling of the material. Each bar, forging, or ring made from titanium or titanium alloy should be clearly marked with relevant information, including the manufacturer's name or trademark, the specification number (AMS 6931), the material type, and the heat or lot number. This identification process is crucial for traceability and quality control purposes.Step 3: Chemical CompositionThe chemical composition of titanium and titanium alloys is critical for determining their mechanical properties and suitability for aerospace applications. AMS 6931 specifies the maximum and minimum limits for various elements, such as carbon, oxygen, iron, and hydrogen, in these materials. These limits ensure that the material possesses the desired strength, corrosion resistance, and other key properties.Step 4: Mechanical PropertiesThe mechanical properties of titanium and titanium alloys, including tensile strength, yield strength, and elongation, play a vital role in aerospace applications as they determine the material's load-bearing capacity, durability, and ability to withstand extreme conditions. AMS 6931 defines the minimum requirements for these properties based on the material's heat treatment condition, size, and form. The standard also provides guidelines for conducting the necessary mechanical tests to verify compliance.Step 5: Metallurgical Structure and Heat TreatmentThe metallurgical structure of titanium and titanium alloys is influenced by the heat treatment processes they undergo. AMS 6931 outlines various heat treatment conditions, such as annealing, solution treatment, and aging, along with the corresponding temperature ranges and cooling procedures. These processes are crucial in optimizing the material's mechanical properties, improving its microstructure, and reducing the risk of defects or failures.Step 6: Nondestructive TestingTo ensure the integrity and reliability of titanium and titanium alloy products, AMS 6931 mandates specific nondestructive testing methods, such as ultrasonic inspection, magnetic particle inspection, and liquid penetrant inspection. These tests help identify any flaws, cracks, or defects that may compromise the material's performance or safety. The standard further details the acceptance criteria for these tests, ensuring consistent quality across all aerospace applications.Step 7: Quality AssuranceAMS 6931 includes provisions for quality assurance, emphasizing the need for manufacturers to establish and maintain an effective quality management system. This system should comprise procedures for material selection, process control, inspection, and documentation to ensure the produced materials meet the standard requirements consistently. The standard also highlights the importance of record keeping for traceability and provides guidelines for supplier qualification and audits.ConclusionAMS 6931 is a comprehensive standard that covers all essential aspects related to titanium and titanium alloy materials used in aerospace applications. Understanding this standard is crucial for manufacturers, suppliers, and engineers involved in the aerospace industry to ensure the highest level of quality, reliability, and performance in aircraft components. By following the step-by-step guidelines outlined in AMS 6931, the aerospace industry can continue to innovate and uphold stringent safety standards in aircraft manufacturing.。

TinuvinCarboProtect-BASFAerospace

TinuvinCarboProtect-BASFAerospace

BASF Aerospace MaterialsTinuvin® CarboProtect®Advanced UV absorber technologyTinuvin CarboProtect is a red-shifted UV-absorber designed for solvent-based clear or semi-transparent coatings over carbon fiber reinforced materials (CFRM) where fibers are embedded in an epoxy matrix or other UV-sensitive substrates. It provides unmatched blocking from destructive UV radiation and protects the composite materials.Performance requirements of aerospace coatings Aerospace coatings must perform in demanding environmental conditions, protect the substrates underneath and provide a beautiful appearance, all at increasingly demanding durability requirements and at coating weights as low as possible. BASF’s Tinuvin CarboProtect advanced UV absorber blocks destructive UV radiation and provides advanced substrates, such as CFRM with protection unmatched by conventional UV absorbers. With this novel technology, it is possible to engineer thinner coatings with increased durability and a maximum in photo-oxidative stability without sacrificing optical quality of the aircraft coatings. Thinner coatings cut down weight and require less drying time, thus reducing fuel consumption and maintenance costs. Furthermore, CFRM substrates are better protected even with pigment-free coatings, allowing the carbon fiber weave to be displayed and utilized as a design element, for example, in parts in the cabin interior.Features and Benefitsn Red-shifted UV absorbern Affords unmatched photo-oxidative stabilityn Protects composites and otherUV-sensitive materialsn Enables thinner, more durable coatings n Enables fuel and maintenance costsavingsFor more information on BASF Aerospace Materials:****************************0.000.250.500.751.001.25290310330350370390410430450Wavelength (nm)A b s o r b a n c eHPT-1BZT-1HPT-2BZT-2020406080100290310330350370390410430450Wavelength (nm)% T r a n s m i t t a n c eTinuvin ® CarboProtect ®369384387391426Figure 1. Absorbance and transmittance of UV absorbers. Solutions of 20 mg/l (absorbance, left) and 80 mg/l (transmittance, right) in chloroform. Method: Perkin Elmer UV/VIS/NIR spectrophotometer Lambda 650. HPT = high performance triazine; BZT = benzo-triazole; the numbers in the graph on the right-hand side indicate the wavelengths where 50% transmittance is observed.Protection of epoxy-based compositesComposites based on aromatic polymers, e.g. carbon fibers in a thermoset aromatic epoxy matrix are inherently lightsensitive. Fundamental studies reveal that critical wavelengths comprise both the UV range (280–380 nm) and the visual range (400–420 nm). No traditional UV absorber technologyprotects as far out as 420 nm to prevent degradation of epoxy-based CFRM. Tinuvin CarboProtect was designed to do just that: based on a very red-shifted, benzotriazole-based technology, its spectral coverage comprises UV-A and UV-B as well as the near visible wavelength range, with a distinct absorption in the UV/Vis area (380–420 nm) as shown in Figure1. It features a high extinction coefficient and excellent photo-permanence.For more information on BASF Aerospace Materials:****************************Weathering experiments illustrate the level of protectionthat Tinuvin CarboProtect provides to CFRM. After 2 yearsof natural weathering in Florida followed by 24 hours of humidity exposure, a CFRM protected by a solvent-based2K PUR coating containing hindered amine light stabilizer (HALS) and a conventional benzotriazole (BZT-3) UV absorber fails a cross-hatch/tape adhesion test catastrophically as illustrated by the whitening and film delamination (Figure 2, top left). Adding a high performance triazine (HPT-1) in addition to BZT-3 improves the UV protection but does not eliminate deterioration as illustrated by strong whitening of the CFRM plaque (Figure 2, top right). The corresponding experiments with Tinuvin CarboProtect instead of the conventional UV absorber do not show any compromised adhesion of the coating nor whitening (Figure 2, bottom left and right), illustrating the superior performance of the advanced,red-shifted UV absorber.Highlight carbon fiber weave in design elements in the cabin interiorThe protection that Tinuvin CarboProtect provides to epoxy-based substrates is so effective that it enables pigment-free, transparent coatings with UV blocking strong enough for exterior applications. In addition, carbon fiber applications used in the cabin interior also require protection from UV radiation and can take advantage of Tinuvin CarboProtect. The option to use transparent coatings over CFRM allows for the carbon fiber weaves to be displayed and utilized as design elements in the cabin interior, for example in wall panels, decorative stripping, and laminating as well as furniture in business jets. For enhanced styling, low levels of pigments can be added to introduce color and metallic or pearlescent effects.Figure 2.Whitening after humidity exposure.Weathering experiments (24 months Floridaexposure) on epoxy-based CFRM, followed by24 h humidity exposure and a cross-hatch/tapeadhesion test. The CFRM were coated withsolvent-based 2K PUR, containing 1% of HALSand the specified types and amounts of UVabsorbers. HPT = high performance triazine;BZT = benzo-triazole.2% BZT-31% HPT-1 2% BZT-3 2% HPT-1 2% Tinuvin® CarboProtect®2.0% Tinuvin®CarboProtect®For more information on BASF Aerospace Materials:****************************BASF Corporation Aerospace Team 100 Campus DriveFlorham Park, NJ 07932E‐mail:****************************Application guidelinesTinuvin CarboProtect is a solid UV absorber, designed for solventborne coatings. While it was originally developed to stabilize carbon fiber reinforced epoxy, it is also suitable for coatings, laminates and plastic substrates as well as base coatings requiring strong protection both in the UV-A range and near visible spectral range.Recommended applications are:n Coatings over carbon or glass fiber reinforced composites (CFRM, GFRM) based on epoxy resin n General coatings or substrates needing protection up to 420 nm n General coatings over substrates very sensitive to UV-A energyFor outdoor applications, Tinuvin CarboProtect should becombined with a hindered amine light stabilizer such as Tinuvin 123 (for acid catalyzed systems) or Tinuvin 292 (for 2K PUR). HALS/UV absorber combinations are synergistic and impart superior coating protection against gloss reduction, cracking, blistering, delamination, and color change. In basecoat/clearcoat systems, Tinuvin CarboProtect UV absorber should be added to the clear coat for maximum efficiency, and the HALS to both the base and the clear coats. For optimum spectral coverage, it can be combined with a triazine-based UV absorber such as Tinuvin 400 (in liquid paints) and Tinuvin 405 (in powder coatings).Binder systemsTinuvin CarboProtect is recommended in binder systems, such as:n 1K and 2K PUR (acrylic/isocyanate, polyester/isocyanate, …)n Thermosetting (acrylic/melamine, polyester/melamine, …)n Thermoplastic (acrylic, vinylic, …)ConcentrationThe concentration of Tinuvin CarboProtect depends on dry film thickness and desired degree of protection. The amount required for optimum performance should be determined in trials covering a concentration range.10–20 μm 10–5%20–40 μm 5–2.5%40–60 μm2.5–1.25%CarboProtect and Tinuvin are trademarks of BASF .Although all statements and information in thispublication are believed to be accurate and reliable, they are presented gratis and for guidance only, and risks and liability for results obtained by use of the products or application of the suggestions described are assumed by the user. NO WARRANTIES OF ANY KIND, EITHER EXPRESSED OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE, ARE MADE REGARDING PRODUCTS DESCRIBED ORDESIGNS, DATA OR INFORMATION SET FORTH. Statements or suggestions concerning possible use of the products are made without representation or warranty that any such use is free of patentinfringement and are not recommendations to infringe any patent. The user should not assume that toxicity data and safety measures are indicated or that other measures may not be required. © 2012 BASF。

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3
Metal Alloys for Aerospace Application
An alloy is a mixture or solid solution of two or more metals. The atoms of one replace the atoms of the other or occupy interstitial positions between the atoms. • • • • • • Aluminum alloys Titanium alloys Steels Magnesium alloys Nickel alloys Beryllium alloys
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Aluminum Alloy Characteristics
• Aluminum alloys are the most widely used materials in aircraft structures. • Al alloys are easily formed and machined. • Al alloys are relatively inexpensive. • Al alloys experience a significant reduction in strength at higher temperatures, limiting their application in supersonic aircraft.
7
Aluminum Alloys
Aluminum alloys are identified by a four-digit numbering system that signifies the primary alloying element. • • • • • • • 1000 2000 3000 4000 5000 6000 7000 99% elemental Al Copper Manganese Silicon Magnesium Magnesium and Silicon Zinc
Shear:
σsu = Ultimate Stress G = Modulus of Rigidity
4
Material Forms for Metals
• Sheet and plate – a rolled, flat product
– Sheet thickness less than 0.250 in. – Plate thickness 0.250 in. or greater
• Extrusion – uniform cross section created by forcing metal through a series of dies • Forging – shape created by plastically deforming metal by compression, usually in closed dies. Forging creates high-strength, tough part with efficient use of material. • Casting – created by solidification of liquid material in a mold
5
Applications for Material Forms
• Sheet and plate
– Sheets are used in skin of fuselage, wings, control surfaces, etc. – Plates are machined to varying thickness create optimum shapes in high-cost parts
Aerospace Materials
• Selection of materials for a given application • Aerospace metal alloys – Properties – Relative costs • Composite materials – Material properties – Analysis methods – Manufacturing
• Group 7000: Compression applications or where static strength is more important than fatigue or damage tolerance
– – – – Upper wing surfaces Wing ribs Floor beams 7075-T6, especially in military jets
11
Steel Alloys
Steel alloys are identified by a four-digit numbering system. The first two digits identify the primary alloying elements, while the last two signify the carbon content. • 4130 • 4340 Cr-Mo with 0.3% C Ni-Cr-Mo with 0.4% C
8
Aluminum Alloys for Airframe Structures
• Group 2000: Primarily in tension applications where fatigue and damage-tolerant design are critical
– Lower wing skins – Pressurized fuselage skins – Standard material has been 2024-T3
9
Titanium Alloys
• Titanium alloys offer, with their higher strength, offer higher structural efficiencies than Al alloys. • Ti alloys are offer selected due to high temperature endurance. • Ti alloys are significantly more expensive than Al (high material cost, more difficult to form and machine). • Galvanic corrosion resistance for fastening composite structures. • The most common alloy is Ti-6Al-4V.
1
Material Selection
The first factor to be considered in selection of a material for a given component is the application. • Operational features – principal function of the component; description of principal loads and environment • Design Criteria – most important design properties for satisfying the operational features • Manufacturing Processes – Material form and fabrication processes.
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Mechanical Properties
Most common metallic materials used for aerospace design are Aluminum, Steel, and Titanium. The properties for these materials are contained in MIL-HDBK-5. Typical data includes:
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Steel Alloys
• Steel contains iron with a small percentage of carbon (0.02 to 1.7%). Other alloying elements are added to achieve specific properties such as strength, toughness, or corrosion resistance. • The mechanical properties of steels can be varied significantly by heat treating. • Some steels offer very high strength. • Steel alloys are not widely used in airframe structures except where very high strength is needed.
Processing used to produce specific properties (such as heat treatment) are designated by a dashed suffix following the four-digit alloy, e.g., 2024-T3.
• Extrusion – used for uniform cross section parts (e.g., stiffeners on spars, ribs) where higher strength is needed • Forging – nonuniform cross section parts where highstrength is needed. • Casting – lower cost parts in noncritical areas
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