ASTM D1003 雾度,透光率

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塑料测试标准实验报告(3篇)

塑料测试标准实验报告(3篇)

第1篇一、实验目的本次实验旨在通过对塑料材料进行一系列标准测试,验证材料的物理、化学及耐久性能,为后续产品设计和应用提供依据。

实验遵循国家及国际相关塑料测试标准,包括但不限于GB/T 16422.3、GB/T 2406-1993、GB/T 2408-1980等。

二、实验材料与设备1. 实验材料:选用某品牌塑料样品,具体型号为PVC(聚氯乙烯)。

2. 实验设备:- 紫外光老化试验箱(符合GB/T 16422.3标准)- 氧指数测定仪(符合GB/T 2406-1993标准)- 水平燃烧法测试仪(符合GB/T 2408-1980标准)- 热变形温度测定仪(符合GB/T 5169.16标准)- 线膨胀系数测定仪(符合GB/T 5169.17标准)三、实验方法与步骤1. UV老化试验:- 将塑料样品放置于紫外光老化试验箱中,分别进行UVA-340和UVB-313EL光照试验。

- 试验周期为1周、2周、4周,观察样品表面变化,记录数据。

2. 氧指数测定:- 按照GB/T 2406-1993标准,对塑料样品进行氧指数测定。

- 将样品置于氧指数测定仪中,设定氧气流量和压力,记录氧指数值。

3. 水平燃烧试验:- 按照GB/T 2408-1980标准,对塑料样品进行水平燃烧试验。

- 将样品放置于水平燃烧法测试仪上,点燃火焰,记录燃烧时间、火焰高度和炭化程度。

4. 热变形温度测定:- 按照GB/T 5169.16标准,对塑料样品进行热变形温度测定。

- 将样品放置于热变形温度测定仪中,设定温度和压力,记录热变形温度。

5. 线膨胀系数测定:- 按照GB/T 5169.17标准,对塑料样品进行线膨胀系数测定。

- 将样品放置于线膨胀系数测定仪中,设定温度和压力,记录线膨胀系数。

四、实验结果与分析1. UV老化试验:- 经过4周UV老化试验后,塑料样品表面出现轻微裂纹和变色,表明该材料具有一定的耐光老化性能。

2. 氧指数测定:- 塑料样品的氧指数为23.5%,符合国家标准要求。

仪电物理 WGW 光电雾度仪 使用说明书

仪电物理  WGW 光电雾度仪 使用说明书

上海仪电物理光学仪器有限公司Shanghai INESA Physico optiacal instrument Co.,LtdWGW 光电雾度仪使用说明书目次1.仪器的用途及特点 (2)2.仪器的使用环境 (2)3.仪器的主要技术指标和规格 (2)4.仪器的结构及原理 (3)5.仪器的操作方法 (3)6.仪器的维护和保养 (4)7.常见故障及其处理方法 (5)8.仪器成套性 (5)9.售后服务事项和生产者责任 (5)本产品根据上海仪电物理光学仪器有限公司企业标准Q310104000005C039《WGW光电雾度仪》生产。

1.仪器的用途及特点WGW光电雾度仪是根据GB/T2410-2008《透明塑料透光率和雾度试验方法》及ASTM D1003-61(1997)设计的小型雾度仪。

适用于平行平板或塑膜样品的测试,能广泛应用于透明、半透明材料雾度、透光率的光学性能检验。

仪器具有结构小巧,使用操作方便的特点。

2.仪器的使用环境A)室温:10℃~30℃b)相对湿度不大于85%;c)无腐蚀性气体;d)无强烈电磁场干扰;e)无直接照射的阳光;f)仪器不应受到影响使用的振动;g)电源:电压220V3.仪器的主要技术指标和规格a)闭式样品舱,样品尺寸50mm×50mm;b)C光源c)测定范围:透光率0%~100%;雾度0%~30%;d)显示方式:LCD312位;e)最小读数:0.1%;f)准确度:透光率±1.5%雾度±0.5%;g)重复性:透光率0.5%雾度0.2%;h)电源:AC220V±22V,频率50Hz±1Hzi)仪器尺寸:L×B×H:470mm×270mm×150mmj)仪器质量(净重):7kg4、仪器的结构及原理仪器的光学系统及电气原理如下:由光源(卤素灯)发出的光经聚光镜会聚在物镜的焦点上。

因此出射的光线为一束平行光。

塑胶测试标准

塑胶测试标准
塑料材料性能测试
检测项目 检测标准
ASTM D2240-05 用硬度计测定橡胶硬度的试验方法 GB/T 2411-1980 塑料邵氏硬度试验方法 ISO 868:2003 塑料 塑料和硬橡胶 用硬度计测定压痕硬度(肖氏硬 度) DIN 53505 橡胶、弹性体和塑料检验 邵氏A和邵氏D硬度试验 ASTM D785-03 塑料与电绝缘材料的洛氏硬度的试验方法
压缩试验中试 样所承受的最 大压缩应力 线性范围内压 缩应力与压缩 应变的比值
性 能
撕裂强度
ASTM D1004-03 塑料薄膜和片材抗初始撕裂试验方法 GB/T 1130-1991 塑料直角撕裂性能试验方法 GB/T 16578-1996 塑料薄膜和薄片耐撕裂性能试验方法 裤形撕 裂法 ISO 6383-1:2004 塑料 薄膜和薄板 耐撕裂性的测定 第1部分:裤 型撕裂法 DIN 53356 人造革和类似的平面织物的检验.连续撕裂试验 ASTM D751-2000 涂层织物的测试方法 GB/T 2792-1998 压敏胶粘带180° 剥离强度试验方法 DIN 53357-1982 塑料布和塑料薄膜的检验.层间分离试验
击 试 验
落锤冲击 落球冲击 验方法:落球法 (/) PV 3905:1972 大众标准 有机材料 落球试验
GB/T 14485-1993 工程塑料硬质塑料板材及塑料件耐冲击性能试
落镖冲击
ASTM D1709-03 自由落镖法测定塑料薄膜抗冲击性能的试验方 法 GB 9639-1988 塑料薄膜和薄片抗冲击性能试验方法 自由落镖 法 SAE J400
在规定的受力 及变形条件 下,测出其显 示脆性破坏时 的温度
燃烧特性 (mm/min)
ASTM D5132-04 机动车宿营舱中用的柔性泡沫和橡胶材料的横 向燃烧速率的测试方法 GB/T 2408-1996 塑料燃烧性能试验方法 水平法和垂直法

塑胶测试标准 (3)

塑胶测试标准 (3)

巴氏硬度 GB/T 3854-1983 纤维增强塑料巴氏(巴柯尔)硬度试验方法
适用各种塑料
适用于回弹性小的 硬质塑料 适用于各种硬质和 软质塑料尤其是纤 维塑料
GB/T 3398-1982 塑料球压痕硬度试验方法
球压痕硬度 ISO 2039-1:2001 塑料 硬度的测定 第一部分:球压痕法
(N/mm2) DIN 53456 塑料检验 球压痕硬度试验
载荷下挠曲温 度
ASTM D648-06 弯曲载荷下塑料变形温度的测定 GB/T 1634.2-2004 塑料 载荷下挠曲温度的测定 第2部分:塑料和 硬橡胶 ISO 75-2:2004 塑料 载荷下挠曲温度的测定 第2部分:塑料和硬橡 胶 DIN 53461 塑料检验 热变形温度的测定 DIN EN ISO 75-2:2004 塑料 载荷下挠曲温度的测定 第2部分:塑 料和硬橡胶塑料
气味试验 (等级)
SAE J1351 GM 9130P GME 60276 通用标准 气味测试 PV 3900-2000 大众标准 气味测试 TSM0505G-2005 丰田标准 FLTM BO 131-01 ES-X 60250 MS 300-34 EDS-T-7603
甲醛含量 (mg/kg)
GME 60271 通用标准 甲醛含量 PV3925 大众标准 甲醛含量 SQR.04.096
ASTM D256-06a 测定塑料悬臂梁试样抗摆锤冲击性能方法
冲 击
悬臂梁冲击 GB/T 1843-1996 塑料悬臂梁冲击试验方法
ISO 180:2001 塑料 悬臂梁冲击性能的测定

验 落锤冲击
落球冲击 (/)
GB/T 14485-1993 工程塑料硬质塑料板材及塑料件耐冲击性能试 验方法:落球法 PV 3905:1972 大众标准 有机材料 落球试验

玻璃和玻璃制品透射雾度测定方法

玻璃和玻璃制品透射雾度测定方法

玻璃和玻璃制品透射雾度测定方法玻璃和玻璃制品透射雾度是指光线通过材料时受到散射的程度。

雾度测定是评估玻璃和玻璃制品透明度的重要方法之一。

下面是50条关于玻璃和玻璃制品透射雾度测定方法的详细描述:1. 根据ASTM D1003-13a标准,使用透射雾度计来测量玻璃和玻璃制品的透射雾度。

2. 准备需要测量的玻璃或玻璃制品样品。

3. 将样品放置在透射雾度计的透射通道中。

4. 调整透射雾度计的参数,如光线强度和测量时间。

5. 开始测量,记录透射雾度计显示的数值。

6. 对于较大的样品,可以使用可移动式透射雾度计进行测量。

7. 确保测量环境的稳定性,避免外部光线影响测量结果。

8. 对于长时间测量,注意保持透射雾度计的稳定性和准确性。

9. 在进行测量之前,清洁透射雾度计的透射通道,以确保测量结果的准确性。

10. 对于有色玻璃或玻璃制品的测量,可以考虑调整透射雾度计的参数或使用滤光片进行校正。

11. 对于不同类型的玻璃或玻璃制品,可以根据需要选择适当的测量方法。

12. 使用合适的测量单位来记录和报告透射雾度测量结果,如百分比或其他符合标准的单位。

13. 对于大批量的玻璃或玻璃制品,可以考虑使用自动化仪器进行透射雾度测量。

14. 确保透射雾度计的标定和校准工作得到定期进行,以确保测量结果的准确性。

15. 在进行测量前,对于不透明或含有颗粒物的样品,需事先处理或准备合适的样品形式。

16. 在测量过程中,确保样品和透射雾度计之间的接触良好,以避免干扰测量结果。

17. 对于较薄的玻璃或玻璃制品,可以考虑使用反射雾度测量方法来评估透射雾度。

18. 选择合适的光源和探测器来保证测量的准确性和重复性。

19. 对于曲面或不规则形状的玻璃或玻璃制品,可以考虑使用透射雾度测量系统进行测量。

20. 在进行测量前,注意样品表面的净化和处理,以避免因表面缺陷或杂质而影响测量结果。

21. 根据需要调整测量时的环境条件,如温度和湿度,以达到准确的测量结果。

透明塑料光穿透率及雾度的标准检测方法

透明塑料光穿透率及雾度的标准检测方法

标识:D 1003– 07Ε透明塑料光穿透率及雾度的标准检测方法本标准以固定标识D1003发放;紧跟在标识后的数字表明初次采用的年代,或最新一次变更年代。

在圆括号内的数字表明了最新一次的批准年代。

上标(ε)表示从上一次批准至今版本上的变动。

本标准已通过美国国防部的批准使用并已取代(实验方法3022-联邦试验方法标准406)1. 范围1.1 本标准涵盖了部分平面材料如透明塑料的穿透率及广角散射的评价方法。

两种方法可用来测量光穿透率和雾度。

方法A使用雾度计中所描述的第5条,方法B使用分光光度计所描述的第8条。

材料的雾度大于30%时即被认为是光散射,此时测试标准就应该依据E167。

1.2 SI单元里出现的数值都将被认作为标准。

标注1-由于一些材料存在小角度高分散率的巨大差别(如磨损的透明塑料),这些材料的雾度校准及测量依据D 1044的测试标准。

1.3 该标准不足以解决所有的安全问题,如果有的话,要结合它的使用。

标准的使用者有责任在使用该标准之前建立适当的安全和健康的管理方法及规定标注2-该测试方法并不等同于ISO 13468-1 和ISO/DIS 147822. 参考文献2.1 ASTM标准:条件作用塑料和电绝缘材料测试的D 618 标准有关塑料专门性的D 883标准电阻式的透明塑料表面磨损测试D1044标准塑料抽样D1898标准物品和材料角度计E 167标准E259半球形和双向定向几何形状白色压粉反射系数转移标准外观标准规范E284实验室内部测试精度标准E 6912.2 ISO 标准:ISO 13468-1 塑料-透明材料透光度总标准ISO/DIS 14782 塑料-透明材料雾度总标准3.专有名词3.1 定义- D883和E284定义的词组适用本测试标准。

3.2 该标准专用的名词:3.2.1 雾度:光传输过程中,透过试样的散射光通量与透射光通量之比。

透射光的百分率是散射光,它在直线方向的偏离角度比入射光的指定角度大。

塑料雾度 标准

塑料雾度 标准

塑料雾度标准一、定义与概念塑料雾度是指塑料制品表面或内部存在的微小凹凸不平或纹理,使光线发生散射,造成制品表面或内部呈现云雾状的模糊现象。

这种雾度不仅影响塑料制品的外观质量,还可能导致其透明度降低,影响使用性能。

因此,对塑料雾度的控制对于提高产品质量和满足客户需求具有重要意义。

二、产生原因塑料雾度的产生原因有多种,主要包括以下几个方面:1.塑料加工过程中的热处理、冷却、结晶等因素可能导致塑料制品表面或内部出现微小的变化,形成雾度。

2.塑料材料的不均匀性,如不同批次材料性能的差异、混合不均匀等,也可能导致雾度的产生。

3.塑料制品的成型工艺参数设置不当,如注射压力、注射速度、模具温度等,也可能影响雾度的形成。

4.塑料制品在使用过程中受到环境因素的影响,如温度变化、光照等,也可能导致雾度的变化。

三、检测方法为了准确测量塑料雾度,可以采用以下几种检测方法:1.目视法:通过肉眼观察塑料制品表面或内部是否存在云雾状的模糊现象,这种方法简单直观,但主观性强,精度不高。

2.光学仪器法:利用光学仪器对塑料制品进行测量,如散射仪、光泽度计等,可以获得较为准确的测量结果。

3.计算机图像处理法:通过计算机对塑料制品的图像进行处理和分析,可以实现对雾度的定量测量。

这种方法具有高精度、高效率等优点,但需要专业的图像处理技术和设备支持。

四、控制方法为了降低塑料雾度,可以采用以下几种控制方法:1.优化加工工艺:通过调整塑料加工过程中的热处理、冷却、结晶等工艺参数,可以降低塑料制品表面或内部的微小变化,从而减少雾度的产生。

同时,优化成型工艺参数设置,如注射压力、注射速度、模具温度等,也可以改善雾度的形成。

2.控制材料质量:加强材料质量控制,确保不同批次材料性能的稳定性和混合均匀性,可以减少因材料不均匀性导致的雾度产生。

3.加强环境控制:在塑料制品使用过程中,加强环境因素的监测和控制,如温度变化、光照等,可以减少环境因素对雾度的影响。

astmd 1003标准

astmd 1003标准

astmd 1003标准
摘要:
1.ASTM D 1003 标准的概述
2.ASTM D 1003 标准的内容
3.ASTM D 1003 标准的应用
4.ASTM D 1003 标准的意义
正文:
ASTM D 1003 标准是由美国材料和试验协会(ASTM)制定的一种标准,主要涉及碳素结构钢的板材、型材和管材的尺寸、形状、重量和允许偏差。

这个标准在全球范围内被广泛采用,是碳素结构钢生产、加工和使用的重要参考依据。

ASTM D 1003 标准的内容非常详细,涵盖了碳素结构钢的各种规格和要求。

例如,标准中规定了板材的厚度、宽度、长度和允许的偏差;型材的截面形状、尺寸和允许的偏差;管材的外径、壁厚、长度和允许的偏差等。

这些规定对于保证碳素结构钢的产品质量、加工和使用具有重要的意义。

ASTM D 1003 标准在碳素结构钢的生产、加工和使用中发挥着重要的作用。

生产厂家可以根据标准规定生产出符合要求的产品,加工企业可以根据标准规定进行加工,使用单位可以根据标准规定选择和使用合适的材料。

同时,标准也可以作为仲裁和解决纠纷的依据。

总的来说,ASTM D 1003 标准对于碳素结构钢的生产、加工和使用具有重要的意义。

WGT-S使用说明书(2010)

WGT-S使用说明书(2010)
1、 仪器的作用
WGT-S 透光率/雾度测定仪是根据中华人民共和国国家标准 GB2410-80“透明塑料 透光率和雾度试验方法”及美国材料试验协会标准 ASTM D1003-61(1997)Standard Test Method for Haze and Luminous Transmittance of Transparent Plastice” 设计的微机化全自 动测量仪器,适用于一切透明、半透明平行平面样器(塑料板材、片材、塑料薄膜、 平板玻璃)的透光率、透射雾度、反射率的测试,也适用于液体样品(水、饮料、药 剂、着色液、油脂)浊度的测量,在国防科研及工农为生产中具有广泛的应用领域。
6、更换样品批号时,应先按测试钮测空白,指示灯转红光,然后仪器将显示“P100.0” 及“H0.00”结果,指示灯显示绿色。一般每测完一组样品应测空白一次,注意测空白 后,应再按测试钮,等到准备灯发绿光、仪器发出呼叫后,再测下一组样品。
7、测试塑膜样品方法不变,只要将薄膜夹于磁性夹具之间稍加拉平,然后即可装 置于样品台上测试,放置夹具时应注意薄膜一面贴紧积分球。
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6、仪器成套性(详见装箱单)
7、售后服务事项和生产者责任
1、本厂产品实行三包,即“包修、包换、包退”。 2、三厂三包期限为一年,以购货发票上时间为准。 3、未按使用说明书操作而操成的仪器损坏,不属于免费服务范围。
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用 WGT-S 透光率/雾度测定仪直接进行质量检测的有: ·光学玻率透光率的测定 ·感光胶片清晰程度的检测 ·人造偏振片偏振度的中间控制 ·航天玻璃、汽车玻璃、防毒面罩玻璃能见度的测定 ·包装塑料薄膜光学综合质量的评定 ·农用塑料薄膜透率的检验 ·建筑、装潢玻璃透光率特性的检查 ·光学投影屏漫射质量的考核 ·电影银幕、投影电视屏幕漫射能力的测定 ·广告灯箱屏幕质量的检验 ·工程描图纸质量的检验 用 WGT-S 透光率/雾度测定仪还可间接应用于: ·毛玻璃洗涤剂质量的评定 ·塑料抛光材料抛光效率的评价 ·凡立斯絮物的测定 ·塑料玻璃罩面抗划伤能力的评价 ·漫射涂料漫无边际射特性的控制及检测 WGT-S 透光率/雾度测定仪用作液体样品浊度测定有: ·纺织厂、热电厂、钢铁厂、灯泡厂、半导体厂、造纸厂、合成纤维厂、工业用 水的检测 ·自来水厂、汽水厂、啤酒厂、糖厂、味精厂、调味品厂食用水、饮料质量检测 ·制药及临床应用于结晶母液中微量固态、物质浓度测定、防疫站对细菌浓度的 测定、血液临床化验、药物透明度的测定等 ·环保部门污水处理质量的检验,海水淡化质量的控制 ·化学工业中着色液浊度之测定,油脂、浊剂浊度之测定 WGT-S 透光率/雾度测定仪具有下列特点: ·技术参数符合 GB2410-80 ASTM D1003-61(1997) JIS K7105-81 等测试标准,

国内聚丙烯牌号(1-3)

国内聚丙烯牌号(1-3)

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附表2:国内外一些大型石化企业聚丙烯牌号一览表
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实用文档
国内外一些大型石化企业聚丙烯牌号一览表(4)
(见Excel表)
说明:
1.由于本书篇幅所限,附表所列只是国内外一些有代表性的大型石化企业所生产的聚丙烯牌号,读者如需更详尽资料可查阅国内近期内出版的一些专著和手册,特别是利用Internet网上各生产企业的网址和从事电子商务公司网址来查询。

2.Montell公司已并入Basell公司,但目前牌号尚未更换。

3.BP Amoco已改名BP Chemicals。

ASTM.塑料标准.D1003

ASTM.塑料标准.D1003

Designation:D1003–00Standard Test Method forHaze and Luminous Transmittance of Transparent Plastics1 This standard is issued under thefixed designation D1003;the number immediately following the designation indicates the year of original adoption or,in the case of revision,the year of last revision.A number in parentheses indicates the year of last reapproval.A superscript epsilon(e)indicates an editorial change since the last revision or reapproval.This test method has been approved for use by agencies of the Department of Defense to replace Method3022of Federal Test Method Standard406.1.Scope1.1This test method covers the evaluation of specific light-transmitting and wide-angle-light-scattering properties of planar sections of materials such as essentially transparent plastic.Two procedures are provided for the measurement of luminous transmittance and haze.Procedure A uses a hazeme-ter as described in Section5and Procedure B uses a spectro-photometer as described in Section8.Material having a haze value greater than30%is considered diffusing and should be tested in accordance with Practice E167.1.2The values stated in SI units are to be regarded as the standard.N OTE1—For greater discrimination among materials that scatter a high percent of light within a narrow forward angle,such as is the case with abraded transparent plastics,adjust the hazemeter and perform measure-ments in accordance with Test Method D1044.1.3This standard does not purport to address all of the safety concerns,if any,associated with its use.It is the responsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.N OTE2—This test method is not equivalent to ISO13468–1and ISO/DIS14782.2.Referenced Documents2.1ASTM Standards:D618Practice for Conditioning Plastics and Electrical Insulating Materials for Testing2D883Terminology Relating to Plastics2D1044Test Method for Resistance of Transparent Plastics to Surface Abrasion2D1898Practice for Sampling of Plastics2E167Practice for Goniophotometry of Objects and Mate-rials3E259Practice for Preparation of Reference White Reflec-tance Standards3E284Terminology of Appearance3E691Practice for Conducting an Interlaboratory Test Pro-gram to Determine the Precision of a Test Method42.2ISO Standards:5ISO13468–1Plastics—Determination of the Total Lumi-nous Transmittance of Transparent MaterialsISO/DIS14782Plastics—Determination of Haze of Trans-parent Materials3.Terminology3.1Definitions—Terms applicable to this test method are defined in Terminologies D883and E284.3.2Definitions of Terms Specific to This Standard:3.2.1haze,n—in transmission,the scattering of light by a specimen responsible for the reduction in contrast of objects viewed through it.The percent of transmitted light that is scattered so that its direction deviates more than a specified angle from the direction of the incident beam.3.2.1.1Discussion—In this test method,the specified angle is0.044rad(2.5°).3.2.2luminous,adj—weighted according to the spectral luminous efficiency function V()of the CIE(1987).3.2.3luminous transmittance,n—the ratio of the luminous flux transmitted by a body to theflux incident upon it.4.Significance and Use4.1Light that is scattered upon passing through afilm or sheet of a material can produce a hazy or smokyfield when objects are viewed through the material.Another effect can be veiling glare,as occurs in an automobile windshield when driving into the sun.4.2Although haze measurements are made most commonly by the use of a hazemeter,a spectrophotometer may be used, provided that it meets the geometric and spectral requirements of Section5.The use of a spectrophotometer for haze mea-surement of plastics can provide valuable diagnostic data on1This test method is under the jurisdiction of ASTM Committee D20on Plastics and is the direct responsibility of Subcommittee D20.40on Optical Properties.Current edition approved June10,2000.Published July2000.Originallypublished as D1003–st previous edition D1003–97e1.2Annual Book of ASTM Standards,V ol08.01.3Annual Book of ASTM Standards,V ol06.01.4Annual Book of ASTM Standards,V ol14.02.5Available from American National Standards Institute,11W.42nd St.,13th Floor,New York,NY10036.1Copyright©ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959,United States.the origin of the haze,6and Procedure B is devoted to the use of a spectrophotometer.4.2.1Procedure A(hazemeter)test values are normally slightly higher and less variable than Procedure B(spectropho-tometer)test values.4.3Regular luminous transmittance is obtained by placing a clear specimen at some distance from the entrance port of the integrating sphere.However,when the specimen is hazy,the total hemispherical luminous transmittance must be measured by placing the specimen at the entrance port of the sphere.The measured total hemispherical luminous transmittance will be greater than the regular luminous transmittance,depending on the optical properties of the sample.With this test method,the specimen is necessarily placed at the entrance port of the sphere in order to measure haze and total hemispherical luminous transmittance.4.4Haze data representative of the material may be ob-tained by avoiding heterogeneous surface or internal defects not characteristic of the material.4.5Haze and luminous-transmittance data are especially useful for quality control and specification purposes.4.6Before proceeding with this test method,reference should be made to the specification of the material being tested. Any test specimen preparation,conditioning,dimensions,or testing parameters,or combination thereof,covered in the materials specification shall take precedence over those men-tioned in this test method.If there are no material specifica-tions,then the default conditions apply.5.Test Specimens5.1Sample the material in accordance with Practice D1898.Obtain specimens that are free of defects not charac-teristic of the material unless such defects constitute variables under study.5.2Cut each test specimen to a size large enough to cover the entrance port of the sphere.A disk50mm(2in.)in diameter,or a square with sides of the same dimensions,is suggested.The specimen shall have substantially plane-parallel surfaces free of dust,grease,scratches,and blemishes,and it shall be free of visibly distinct internal voids and particles, unless it is specifically desired to measure the contribution to haze due to these imperfections.5.3Prepare three specimens to test each sample of a given material unless specified otherwise in the applicable material specification.6.Conditioning6.1Conditioning—Unless otherwise required in the appro-priate materials specification or agreed between customer/ supplier,condition the test specimens at2362°C(73.46 3.6°F)and5065%relative humidity for not less than40h prior to test,in accordance with Procedure A of Practice D618. In case of disagreements,the tolerances shall be61°C(1.8°F) and62%relative humidity.6.2Test Conditions—Set up the test apparatus in an atmo-sphere maintained at2362°C(73.463.6°F)and5065% relative humidity.7.Procedure A—Hazemeter7.1Apparatus:7.1.1The instrument used for measurement shall meet the geometric and spectral requirements of this section.77.1.2A light source and a photodetector shall be supplied, and the combination shall befiltered to provide an output corresponding to the luminosity response of the1931CIE Standard Colorimetric Observer with CIE Standard Illuminant C or,alternatively,Illuminant A.The output shall be propor-tional to within1%to the incidentflux over the range offlux used.The photometric stability for source and detector must be constant throughout the test of each specimen.7.1.3Use an integrating sphere to collect transmittedflux; the sphere may be of any diameter as long as the total port areas do not exceed4.0%of the internal reflecting area of the sphere.The entrance and exit ports shall be centered on the same great circle of the sphere,and there shall be at least2.97 rad(170°)of arc between centers.The exit port shall subtend an angle of0.14rad(8°)at the center of the entrance port.With the light trap in position,without the specimen,the axis of the irradiating beam shall pass through the centers of the entrance and exit ports.For a hazemeter,position the photocell or photocells on the sphere1.5760.17rad(90610°)from the entrance port and baffle it from direct exposure to the entrance port.In the pivotable modification where the interior wall adjacent to the exit port is used as the reflectance reference,the angle of rotation of the sphere shall be0.14060.008rad(8.0 60.5°).7.1.4Illuminate the specimen by a substantially unidirec-tional beam;the maximum angle that any ray of this beam may make with the beam axis shall not exceed0.05rad(3°).This beam shall not be vignetted at either port of the sphere.7.1.5When the specimen is placed against the entrance port of the integrating sphere,the angle between the perpendicular to the specimen and a line connecting the centers of entrance and exit ports shall not exceed0.14rad(8°).7.1.6When the beam is unobstructed by a specimen,its cross section at the exit port shall be approximately circular, sharply defined,and concentric within the exit port,leaving an annulus of0.02360.002rad(1.360.1°)subtended at the entrance port.N OTE3—It is important to verify whether the unobstructed-beam diameter and centering at the exit port are maintained,especially if the source aperture and focus are changed.N OTE4—The tolerance stated on the annulus of0.002rad(0.1°) corresponds to an uncertainty of60.6%in a haze reading.8This is relevant for assessing the precision and bias of this test method.6Billmeyer,F.W.,Jr.,and Chen,Y.,“On the Measurement of Haze,”Color Research and Application,V ol10,1985,pp.219–224.7Hazemeters made by BYK-Gardner,Inc.,2435Linden Lane,Silver Spring, MD20910,meet these requirements.Other manufacturers of this equipment,which meet the requirements,may exist but have not been identified.8Weidner,V.R.,and Hsia,J.J.,“NBS Reference Hazemeter:Its Development and Testing,”Applied Optics,V ol18,1979,pp.1619–1626.7.1.7The surfaces of the interior of the integrating sphere,baffles,and reflectance standard,if used,shall be of equal reflectance,matte,and highly reflecting throughout the visible spectrum.97.1.8A light trap shall be provided that will absorb the beam completely when no specimen is present,or the instrument design shall obviate the need for a light trap.7.1.9A schematic drawing of the optics of a hazemeter with unidirectional illumination and diffuse viewing is shown in Fig.1.7.1.10A series of calibrated haze standards is required for periodic verification of the accuracy of instrumental response.Ideally,if the haze of narrow-angle-scattering specimens (such as plastic films)is to be measured,narrow-angle-scattering glass standards should be used;7,8however,these are not known to be commercially available.In their absence,wide-angle-plastic standards 10may be used,but these are less sensitive to the size and centering of the annulus described by Billmeyer and Chen 6and Weidner and Hsia,9and particular attention should be paid to Note 1when only plastic haze standards are used.7.2Procedure :7.2.1Determine the following four readings:Reading DesignationSpecimen in PositionLight Trap in PositionReflectance Standard in PositionQuantity Represented T 1no no yes incident lightT 2yes no yes total light transmitted by specimenT 3no yes no light scattered by instru-mentT 4yesyesnolight scattered by instru-ment and specimen7.2.2Repeat readings for T 1,T 2,T 3,and T 4with additional specified positions of the specimen to determine uniformity.7.3Calculation 11:7.3.1Calculate total transmittance,T t (Note 5),equal to T 2/T 1.7.3.2Calculate diffuse transmittance,T d (Note 5),as fol-lows:T d 5@T 42T 3~T 2/T 1!#/T 1(1)7.3.3Calculate percent haze as follows:haze 5T d /T t 3100(2)N OTE 5—To obtain the greatest accuracy in luminous transmittance measurement when using a single-beam instrument,it is necessary to use a standard,calibrated with a double-beam instrument,because insertion of the sample in the single-beam instrument changes the efficiency of the sphere.This change may result in spuriously high readings for clear,colorless samples and significant errors for dark or highly saturated colors.In these cases,the photometer should be used as a comparison instrument with a standard of known transmittance similar to that of the specimen.For greatest accuracy of luminous transmittance measurement,compare the transmittance of the specimen with that of a calibrated standard of similar luminous transmittance.7.4Report :7.4.1Report the following data:7.4.1.1Source and identity of specimen,7.4.1.2Nominal thickness of specimen to the nearest 0.025mm,7.4.1.3Total luminous transmittance,T t ,to the nearest 0.1%(indicate the average when reporting average values and specify whether CIE Illuminant C or A is used),7.4.1.4Diffuse luminous transmittance,T d ,to the nearest 0.1%(indicate the average when reporting average values),and7.4.1.5Percent haze,to the nearest 0.1%(indicate the average when reporting average values).7.5Precision and Bias—Hazemeter :7.5.1Precision :7.5.1.1Table 1and Table 2are based on a round robin conducted in 1985,in accordance with Practice E 691,involv-ing six film materials tested by 11laboratories.In the round robin,each laboratory that measured a property made eight replicate measurements of the property for each of the six materials listed as 1to 6in Table 1and Table 2.7.5.1.2Table 3is based on a round robin conducted in 1991involving eight materials and six laboratories.This table can be directly compared to Table 4(Spectrophotometer).N OTE 6—Caution:The following explanations of r and R (7.5.1.3-7.5.1.7)are intended to present only a meaningful way of considering the approximate precision of this test method.The data in Tables 1-3should not be applied rigorously to acceptance or rejection of material,as those data are specific to the round robin and may not be representative of other9Highly reflective matte barium sulfate paint or pressed polytetrafluoroethylene powder are excellent for this purpose.See Practice E 259.10Calibrated plastic haze standards are available from BYK-Gardner,Inc.,2435Linden Lane,Silver Spring,MD 20910.11See Appendix X1for derivation offormulas.FIG.1Schematic of HazemeterTABLE 1Summary of 1985Procedure A (Hazemeter)Total HazeRound Robin Involving Eleven LaboratoriesMaterial Average S(r)S(R)r R 3 3.80.100.330.280.9418.70.180.420.50 1.18213.50.080.400.23 1.12418.00.270.610.76 1.72521.00.41 1.68 1.16 4.74626.50.351.130.983.19lots,conditions,materials,or ers of this test method should apply the principles outlined in Practice E 691to generate data specific to their laboratory and materials,or between specific laboratories.The principles of 7.5.1.3-7.5.1.7would then be valid for such data.7.5.1.3For the purpose of compiling summary statistics,a test result has been defined to be the average of three replicate measurements of a property for a material in a laboratory,as specified in this test method.Summary statistics are given in Tables 1-3.In each table,for the material indicated,S(r)is the pooled within-laboratory standard deviation of a test result,S(R)is the between-laboratory standard deviation of a test result,r =2.833S(r)(see 7.5.1.4),and R =2.833S(R)(see 7.5.1.5).7.5.1.4Repeatability —Two test results obtained within one laboratory shall be judged not equivalent if they differ by morethan the “r ”value for that material.“r ”is the interval representing the critical difference between two test results for the same material,obtained by the same operator using the same equipment on the same day in the same laboratory.7.5.1.5Reproducibility —Two test results obtained by dif-ferent laboratories shall be judged not equivalent if they differ by more than the “R ”value for that material.“R ”is the interval representing the critical difference between two test results for the same material,obtained by different operators using differ-ent equipment in different laboratories.7.5.1.6Judgments made as described in 7.5.1.3and 7.5.1.4will be correct in approximately 95%of such comparisons.7.5.1.7For further information,see Practice E 691.7.5.2Bias —Measurement biases cannot be determined since there are no accepted referee methods for determining these properties.8.Procedure B (Spectrophotometer)8.1Apparatus :8.1.1The instruments used for measurement shall meet the geometric and spectral requirement of this section.8.1.2The instrument shall be capable of computing from the spectral data the 1931CIE tristimulus values and related color coordinates for CIE standard Illuminant C or alterna-tively Illuminant A.8.1.3The instrument shall utilize a hemispherical optical measuring system,with an integrating sphere,in which the specimen can be placed flush against the sphere port.The surfaces of the interior of the integrating sphere,baffles,and reflectance standards shall be matte,of substantially equal reflectance and highly reflecting throughout the visible wave-lengths.8.1.4Two geometries can be used:unidirectional illumina-tion with diffuse viewing and diffuse illumination with unidi-rectional ing Geometry B the following apply:8.1.4.1Use an integrating sphere to illuminate the specimen diffusely;the sphere may be of any diameter as long as the total port areas do not exceed 4.0%of the internal reflecting area of the sphere.The specimen and light trap ports of the sphere shall be centered on the same great circle of the sphere,and there shall be at least 2.97rad (170°)of arc between their centers.The light trap port shall subtend an angle of 0.14rad (8°)at the center of the specimen port along the wowing beam.With the light trap in position,without specimen the axis of the viewing beam shall pass through the centers of the specimen and light trap ports.8.1.4.2View the specimen along an axis defined by a substantially unidirectional beam;the maximum angle that any ray of this beam may make with the beam axis shall not exceed 0.05rad (3°).This beam shall not be vignetted at either port of the sphere.8.1.4.3When the specimen is in place,the angle between the specimen normal and the line connecting the centers of the specimen and the light trap ports shall not exceed 0.14rad (8°).8.1.4.4With no specimen in place,the viewed area at the exit port shall be approximately circular,sharply defined concentric within the light trap port,leaving an annulus of 0.02360.002rad (1.360.01°)subtended at the specimen port.TABLE 2Summary of 1985Procedure A (Hazemeter)Luminous Transmittance Round Robin Involving Eleven LaboratoriesMaterial Average S(r)S(R)r R 283.60.25 1.210.69 3.42484.80.15 1.060.42 3.02186.40.08 1.080.22 3.06387.50.20 1.070.57 3.02688.50.14 2.100.38 5.93588.60.352.230.996.32TABLE 3Summary of 1991Procedure A (Hazemeter)Total HazeRound Robin Involving Six LaboratoriesMaterial Average S(r)S(R)r R LDPE A 0.580.0310.1330.0860.372B 1.890.0290.2160.0800.604C 2.080.0210.2000.0580.568PET D 2.690.0420.3130.1170.075E 5.740.0310.3950.086 1.106F 8.060.0490.5660.137 1.584G 12.680.0500.4900.140 1.372H28.570.0911.0420.2562.9918TABLE 4Summary of 1991Procedure B (Spectrophotometer)Total Haze Round Robin Involving Seven LaboratoriesMaterial Average S(r)A S(R)B r C R D LDPE A 0.550.0760.1860.2130.522B 1.770.0870.6580.244 1.019C 1.010.0420.3970.175 1.112PET D 2.510.1150.3310.3230.927E 5.050.0810.5960.227 1.669F 6.550.189 1.1380.305 3.186G 11.350.137 1.2890.385 3.610H25.450.1583.0200.4438.455AS r is the within laboratory standard deviation for the indicated material.It is obtained by pooling the within-laboratory standard deviations of the test results from all of the participating laboratories:S r 5@@~s 1!21~s 2!2...1~s n !2#/n #½BS R is the between laboratories reproducibility,expressed as standard devia-tion:S R 5@s r 21s L 2#½where:s L =standard deviation of laboratory means.Cr is the within-laboratory critical interval between two test results =2.83S r .DR is the between-laboratories critical interval between two test results =2.83S R.N OTE 7—Note 3and Note 4apply.It should be noted that it may be difficult,but is critical,to meet this requirement.8.1.5A light trap shall be provided that will completely absorb the beam when no specimen is present,or the instru-ment design shall obviate the need for a light trap.8.1.6A schematic drawing of a spectrophotometer with unidirectional illumination and diffuse viewing is shown in Fig.2.N OTE 8—It is strongly recommended that conformance to the intent of this test method be confirmed through use of properly calibrated haze standards due to the difficulty of confirming conformance to this test method when using a drill spectrophotometer.8.2Procedure —Follow the manufacturer’s instructions for the measurement of haze,and if none available,use Section 8.8.3Calculation —Most spectrophotometers are computer driven and values for luminous transmission and haze are automatically calculated.If values are not computed use calculation method in Section 9.8.4Report :8.4.1Report the following data:8.4.1.1Source and identity of specimen,8.4.1.2Nominal thickness of specimen,8.4.1.3Percent haze,to the nearest 0.1%(indicate the average when reporting average values),8.4.1.4Total luminous transmittance,T t ,to the nearest 0.1%(indicate the average when reporting average values and specify whether CIE Illuminant C or A is used)when specifi-cally requested,and8.4.1.5Diffuse luminous transmittance,T d ,to the nearest 0.1%(indicate the average when reporting average values)when specifically requested.8.5Precision and Bias :8.5.1Precision :8.5.1.1Precision data in Table 4is based on a round robin conducted in 1991involving eight materials and seven labo-ratories.For comparison purposes the same materials were measured on six regular hazemeters during the same round robin.The data from the regular hazemeter round robin is included in Table 3.N OTE 9—Caution:The following explanations of r and R (8.5.1.2-8.5.1.6)are intended to present only a meaningful way of considering the approximate precision of this test method.The data in Tables 1-4should not be applied rigorously to acceptance or rejection of material,as those data are specific to the round robin and may not be representative of other lots,conditions,materials,or ers of this test method should apply the principles outlined in Practice E 691to generate data specific to their laboratory and materials,or between specific laboratories.The principles of 8.5.1.2-8.5.1.6would then be valid for such data.8.5.1.2For the purpose of compiling summary statistics,a test result has been defined to be the average of three replicate measurements of a property for a material in a laboratory,as specified in this test method.Summary statistics are given in Table 4.In each table,for the material indicated,S(r)is the pooled within-laboratory standard deviation of a test result,S(R)is the between-laboratory standard deviation of a test result,r =2.833S(r)(see 8.5.1.3),and R =2.833S(R)(see 8.5.1.4).8.5.1.3Repeatability —In comparing two mean values of the same material,obtained by the same operator using the same equipment on the same day,the means should be judged not equivalent if they differ by more than the r value for that material.8.5.1.4Reproducibility —In comparing two mean values for the same material obtained by different operators using differ-ent equipment on different days,either in the same laboratory or in different laboratories,the means should be judged not equivalent if they differ by more than the R value for that material.8.5.1.5Judgments made as described in 8.5.1.3and 8.5.1.4will be correct in approximately 95%of such comparisons.8.5.1.6For further information,see Practice E 691.8.5.2Bias —Measurement biases cannot be determined since there are no accepted referee methods for determining these properties.9.Referee Procedure9.1In case of dispute,Procedure A—Hazemeter will be the referee procedure measured with a standard hazemeter.10.Keywords10.1haze;luminous transmittance;regular transmittance;transparentplasticsFIG.2Spectrophotometer With DiffuseIlluminationAPPENDIXES(Nonmandatory Information)X1.DERIV ATION OF FORMULAS FOR HAZEX1.1The derivation of the formula for haze for both procedures is as follows:X1.1.1Total luminous transmittance,T t,is calculated as follows:T t5T2/T1(X1.1)where:T2=total light transmitted by the specimen,andT1=incident light.X1.1.2If T3,the light scattered by the instrument,is zero, the diffuse luminous transmittance,T d,is calculated as follows:T d5T4/T1(X1.2)where:T4=light scattered by the instrument and specimen.X1.1.3If T3is greater than zero due to light scattered by the instrument,the total scattered light,T4,will be greater than the light scattered by the specimen by an amount proportional to T3 and equal to T3times T2/T1.The corrected amount of light scattered by the specimen will then be the following:T42T3~T2/T1!(X1.3) X1.1.4The diffuse luminous transmittance,T d,is then calculated as follows:T d5@T42T3~T2/T1!#/T1(X1.4) X1.1.5Percent haze is then calculated from the ratio of diffuse,T d,to total luminous transmittance,T t,as follows:haze,%5~T d/T t!3100(X1.5) 5@~T42T3~T2/T1!#/T14~T2/T1!#31005@~T42T3~T2/T1!#/T2!31005@~T4/T2!2~T3/T1!#3100X2.ALTERNATIVE HAZE(SHORTCUT)PROCEDUREX2.1Many commercial hazemeters have indicating sys-tems and a means of adjusting the light scattered by the instrument to zero and the total light transmitted by the specimen to100.For these instruments,the following is a shortcut method that can be used for determining haze.N OTE X2.1—This shortcut procedure may produce erroneous values for highly absorbing samples,or those measured in a stopped-down beam mode(as for Tabor abrasion haze).With such samples,instrument stray light may not be properly accounted for.It is recommended that in such situations a comparison be made of the standard procedure and the shortcut procedure using typical samples.In case of any disagreement,the standard procedure shall be considered to produce the correct values.X2.1.1With the hazemeter set to measure total transmit-tance,adjust the instrument output to read100.0.X2.1.2With the hazemeter set to measure light scattered by the instrument,adjust the instrument output to read0.0.X2.1.3With the hazemeter set to measure total transmit-tance,place the test specimen against the entrance port of the integrating sphere.X2.1.4Adjust the instrument output to read100.0.X2.1.5Set the instrument to measure light scattered by the specimen and record the reading as percent haze.ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentioned in this ers of this standard are expressly advised that determination of the validity of any such patent rights,and the risk of infringement of such rights,are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed everyfive years and if not revised,either reapproved or withdrawn.Your comments are invited either for revision of this standard or for additional standards and should be addressed to ASTM International Headquarters.Your comments will receive careful consideration at a meeting of the responsible technical committee,which you may attend.If you feel that your comments have not received a fair hearing you should make your views known to the ASTM Committee on Standards,at the address shown below.This standard is copyrighted by ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959, United States.Individual reprints(single or multiple copies)of this standard may be obtained by contacting ASTM at the above address or at610-832-9585(phone),610-832-9555(fax),or service@(e-mail);or through the ASTM website().。

透明塑料光穿透率及雾度的标准检测方法.

透明塑料光穿透率及雾度的标准检测方法.

标识:D 1003–07Ε透明塑料光穿透率及雾度的标准检测方法本标准以固定标识 D1003发放;紧跟在标识后的数字表明初次采用的年代,或最新一次变更年代。

在圆括号内的数字表明了最新一次的批准年代。

上标(ε 表示从上一次批准至今版本上的变动。

本标准已通过美国国防部的批准使用并已取代(实验方法 3022-联邦试验方法标准 4061. 范围1.1 本标准涵盖了部分平面材料如透明塑料的穿透率及广角散射的评价方法。

两种方法可用来测量光穿透率和雾度。

方法 A 使用雾度计中所描述的第 5条 ,方法 B 使用分光光度计所描述的第 8条。

材料的雾度大于 30%时即被认为是光散射,此时测试标准就应该依据 E167。

1.2 SI 单元里出现的数值都将被认作为标准。

标注 1-由于一些材料存在小角度高分散率的巨大差别(如磨损的透明塑料 ,这些材料的雾度校准及测量依据 D 1044的测试标准。

1.3 该标准不足以解决所有的安全问题,如果有的话,要结合它的使用。

标准的使用者有责任在使用该标准之前建立适当的安全和健康的管理方法及规定标注 2-该测试方法并不等同于 ISO 13468-1 和 ISO/DIS 147822. 参考文献2.1 ASTM 标准:条件作用塑料和电绝缘材料测试的 D 618 标准有关塑料专门性的 D 883标准电阻式的透明塑料表面磨损测试 D1044标准塑料抽样 D1898标准物品和材料角度计 E 167标准E259半球形和双向定向几何形状白色压粉反射系数转移标准外观标准规范 E284实验室内部测试精度标准 E 6912.2 ISO 标准:ISO 13468-1 塑料 -透明材料透光度总标准ISO/DIS 14782 塑料 -透明材料雾度总标准3.专有名词3.1 定义 - D883和 E284定义的词组适用本测试标准。

3.2 该标准专用的名词:3.2.1 雾度:光传输过程中,透过试样的散射光通量与透射光通量之比。

导光级PC,高流动导光PC

导光级PC,高流动导光PC

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体积流动速率(MVR ) 力学性能
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ISO 1133 (JIS K7210)
300℃ 1.20kg 4
拉伸(屈服)强度 *1 拉伸断裂应变*2 弯弯曲曲强弹度性率
简支梁冲击强 度
洛氏硬度 热性能
MPa % MPa GPa kJ/m2

ISO 527-1,2 (JIS K7161, 7162)ISO 178
LC2200 >PC<
1.2 0.23
300℃ 1.20kg 12
Y65 tB95 90 2.3 80
R120/M50
- 129 6.5 0.5~0.7
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280~320℃ (上限320℃) 80~120℃ 120℃、5~8时 间
耐光性 高耐水蒸汽
LEV1700 >PC< 1.2 0.23
Y50 tB70 80 2.2 30

136 125 6.5 0.5~0.6
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Y60 tB60 90 2.6 15
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UL94 UL746A
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astmd 1003标准

astmd 1003标准

astmd 1003标准ASTM D1003标准是用于测试透明或透光材料的透光度的标准。

这个标准适用于任何透明或透光材料,包括塑料、玻璃、涂料、薄膜等。

透光度是一个描述材料光透过能力的物理特性,它是通过测量光线通过材料时的亮度来确定的。

这个标准通过使用特定的光波长、光源和光探测器来测量透光度,以确保结果的准确性和可重复性。

ASTM D1003标准主要包含了三种测量透光度的方法:透光度测试、透光度差测试和透光度变化测试。

透光度测试是最常用的方法,它通过测量光线通过材料时的透射亮度来计算透光度。

透光度差测试是测量不同区域或不同材料的透光度差异,用于评估产品的均匀性。

透光度变化测试是测量材料在不同光照条件下的透光度变化,用于评估材料的稳定性和耐久性。

在ASTM D1003标准中,还规定了测试所需的设备和样品准备方法。

样品应该是充分代表材料特性的代表性样品,并且在测试前应该进行必要的处理,如切割、磨光、清洁等。

测试设备应满足一定的规范要求,包括使用合适的光源、光波长和光探测器等。

为了保证测试结果的准确性和可重复性,ASTM D1003标准还规定了测试的环境条件和操作要求。

测试应该在恒定的温度和湿度条件下进行,并且操作人员应该经过培训并熟悉测试方法和操作步骤。

ASTM D1003标准的应用非常广泛,它可以用于质量控制、产品开发、研究和比较不同材料的透光性能等方面。

例如,在塑料制品行业,透光度是一个重要的性能指标,它可以影响产品的质量和外观。

通过使用ASTM D1003标准,可以对不同材料进行透光度测试,并选择适合的材料用于生产。

另外,ASTM D1003标准还可以用于研究透光材料的性能特点,如光透过机制、光散射等,以指导新材料的设计和开发。

总之,ASTM D1003标准是一个用于测试透明或透光材料透光度的标准,它提供了测量方法和规范,以确保测试结果的准确性和可重复性。

这个标准在质量控制、产品开发和研究等领域都有广泛的应用,对于评估材料的透光性能具有重要的意义。

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Designation:D1003–00Standard Test Method forHaze and Luminous Transmittance of Transparent Plastics1 This standard is issued under thefixed designation D1003;the number immediately following the designation indicates the year of original adoption or,in the case of revision,the year of last revision.A number in parentheses indicates the year of last reapproval.A superscript epsilon(e)indicates an editorial change since the last revision or reapproval.This test method has been approved for use by agencies of the Department of Defense to replace Method3022of Federal Test Method Standard406.1.Scope1.1This test method covers the evaluation of specific light-transmitting and wide-angle-light-scattering properties of planar sections of materials such as essentially transparent plastic.Two procedures are provided for the measurement of luminous transmittance and haze.Procedure A uses a hazeme-ter as described in Section5and Procedure B uses a spectro-photometer as described in Section8.Material having a haze value greater than30%is considered diffusing and should be tested in accordance with Practice E167.1.2The values stated in SI units are to be regarded as the standard.N OTE1—For greater discrimination among materials that scatter a high percent of light within a narrow forward angle,such as is the case with abraded transparent plastics,adjust the hazemeter and perform measure-ments in accordance with Test Method D1044.1.3This standard does not purport to address all of the safety concerns,if any,associated with its use.It is the responsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.N OTE2—This test method is not equivalent to ISO13468–1and ISO/DIS14782.2.Referenced Documents2.1ASTM Standards:D618Practice for Conditioning Plastics and Electrical Insulating Materials for Testing2D883Terminology Relating to Plastics2D1044Test Method for Resistance of Transparent Plastics to Surface Abrasion2D1898Practice for Sampling of Plastics2E167Practice for Goniophotometry of Objects and Mate-rials3E259Practice for Preparation of Reference White Reflec-tance Standards3E284Terminology of Appearance3E691Practice for Conducting an Interlaboratory Test Pro-gram to Determine the Precision of a Test Method42.2ISO Standards:5ISO13468–1Plastics—Determination of the Total Lumi-nous Transmittance of Transparent MaterialsISO/DIS14782Plastics—Determination of Haze of Trans-parent Materials3.Terminology3.1Definitions—Terms applicable to this test method are defined in Terminologies D883and E284.3.2Definitions of Terms Specific to This Standard:3.2.1haze,n—in transmission,the scattering of light by a specimen responsible for the reduction in contrast of objects viewed through it.The percent of transmitted light that is scattered so that its direction deviates more than a specified angle from the direction of the incident beam.3.2.1.1Discussion—In this test method,the specified angle is0.044rad(2.5°).3.2.2luminous,adj—weighted according to the spectral luminous efficiency function V()of the CIE(1987).3.2.3luminous transmittance,n—the ratio of the luminous flux transmitted by a body to theflux incident upon it.4.Significance and Use4.1Light that is scattered upon passing through afilm or sheet of a material can produce a hazy or smokyfield when objects are viewed through the material.Another effect can be veiling glare,as occurs in an automobile windshield when driving into the sun.4.2Although haze measurements are made most commonly by the use of a hazemeter,a spectrophotometer may be used, provided that it meets the geometric and spectral requirements of Section5.The use of a spectrophotometer for haze mea-surement of plastics can provide valuable diagnostic data on1This test method is under the jurisdiction of ASTM Committee D20on Plastics and is the direct responsibility of Subcommittee D20.40on Optical Properties.Current edition approved June10,2000.Published July2000.Originallypublished as D1003–st previous edition D1003–97e1.2Annual Book of ASTM Standards,V ol08.01.3Annual Book of ASTM Standards,V ol06.01.4Annual Book of ASTM Standards,V ol14.02.5Available from American National Standards Institute,11W.42nd St.,13th Floor,New York,NY10036.1Copyright©ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959,United States.the origin of the haze,6and Procedure B is devoted to the use of a spectrophotometer.4.2.1Procedure A(hazemeter)test values are normally slightly higher and less variable than Procedure B(spectropho-tometer)test values.4.3Regular luminous transmittance is obtained by placing a clear specimen at some distance from the entrance port of the integrating sphere.However,when the specimen is hazy,the total hemispherical luminous transmittance must be measured by placing the specimen at the entrance port of the sphere.The measured total hemispherical luminous transmittance will be greater than the regular luminous transmittance,depending on the optical properties of the sample.With this test method,the specimen is necessarily placed at the entrance port of the sphere in order to measure haze and total hemispherical luminous transmittance.4.4Haze data representative of the material may be ob-tained by avoiding heterogeneous surface or internal defects not characteristic of the material.4.5Haze and luminous-transmittance data are especially useful for quality control and specification purposes.4.6Before proceeding with this test method,reference should be made to the specification of the material being tested. Any test specimen preparation,conditioning,dimensions,or testing parameters,or combination thereof,covered in the materials specification shall take precedence over those men-tioned in this test method.If there are no material specifica-tions,then the default conditions apply.5.Test Specimens5.1Sample the material in accordance with Practice D1898.Obtain specimens that are free of defects not charac-teristic of the material unless such defects constitute variables under study.5.2Cut each test specimen to a size large enough to cover the entrance port of the sphere.A disk50mm(2in.)in diameter,or a square with sides of the same dimensions,is suggested.The specimen shall have substantially plane-parallel surfaces free of dust,grease,scratches,and blemishes,and it shall be free of visibly distinct internal voids and particles, unless it is specifically desired to measure the contribution to haze due to these imperfections.5.3Prepare three specimens to test each sample of a given material unless specified otherwise in the applicable material specification.6.Conditioning6.1Conditioning—Unless otherwise required in the appro-priate materials specification or agreed between customer/ supplier,condition the test specimens at2362°C(73.46 3.6°F)and5065%relative humidity for not less than40h prior to test,in accordance with Procedure A of Practice D618. In case of disagreements,the tolerances shall be61°C(1.8°F) and62%relative humidity.6.2Test Conditions—Set up the test apparatus in an atmo-sphere maintained at2362°C(73.463.6°F)and5065% relative humidity.7.Procedure A—Hazemeter7.1Apparatus:7.1.1The instrument used for measurement shall meet the geometric and spectral requirements of this section.77.1.2A light source and a photodetector shall be supplied, and the combination shall befiltered to provide an output corresponding to the luminosity response of the1931CIE Standard Colorimetric Observer with CIE Standard Illuminant C or,alternatively,Illuminant A.The output shall be propor-tional to within1%to the incidentflux over the range offlux used.The photometric stability for source and detector must be constant throughout the test of each specimen.7.1.3Use an integrating sphere to collect transmittedflux; the sphere may be of any diameter as long as the total port areas do not exceed4.0%of the internal reflecting area of the sphere.The entrance and exit ports shall be centered on the same great circle of the sphere,and there shall be at least2.97 rad(170°)of arc between centers.The exit port shall subtend an angle of0.14rad(8°)at the center of the entrance port.With the light trap in position,without the specimen,the axis of the irradiating beam shall pass through the centers of the entrance and exit ports.For a hazemeter,position the photocell or photocells on the sphere1.5760.17rad(90610°)from the entrance port and baffle it from direct exposure to the entrance port.In the pivotable modification where the interior wall adjacent to the exit port is used as the reflectance reference,the angle of rotation of the sphere shall be0.14060.008rad(8.0 60.5°).7.1.4Illuminate the specimen by a substantially unidirec-tional beam;the maximum angle that any ray of this beam may make with the beam axis shall not exceed0.05rad(3°).This beam shall not be vignetted at either port of the sphere.7.1.5When the specimen is placed against the entrance port of the integrating sphere,the angle between the perpendicular to the specimen and a line connecting the centers of entrance and exit ports shall not exceed0.14rad(8°).7.1.6When the beam is unobstructed by a specimen,its cross section at the exit port shall be approximately circular, sharply defined,and concentric within the exit port,leaving an annulus of0.02360.002rad(1.360.1°)subtended at the entrance port.N OTE3—It is important to verify whether the unobstructed-beam diameter and centering at the exit port are maintained,especially if the source aperture and focus are changed.N OTE4—The tolerance stated on the annulus of0.002rad(0.1°) corresponds to an uncertainty of60.6%in a haze reading.8This is relevant for assessing the precision and bias of this test method.6Billmeyer,F.W.,Jr.,and Chen,Y.,“On the Measurement of Haze,”Color Research and Application,V ol10,1985,pp.219–224.7Hazemeters made by BYK-Gardner,Inc.,2435Linden Lane,Silver Spring, MD20910,meet these requirements.Other manufacturers of this equipment,which meet the requirements,may exist but have not been identified.8Weidner,V.R.,and Hsia,J.J.,“NBS Reference Hazemeter:Its Development and Testing,”Applied Optics,V ol18,1979,pp.1619–1626.7.1.7The surfaces of the interior of the integrating sphere,baffles,and reflectance standard,if used,shall be of equal reflectance,matte,and highly reflecting throughout the visible spectrum.97.1.8A light trap shall be provided that will absorb the beam completely when no specimen is present,or the instrument design shall obviate the need for a light trap.7.1.9A schematic drawing of the optics of a hazemeter with unidirectional illumination and diffuse viewing is shown in Fig.1.7.1.10A series of calibrated haze standards is required for periodic verification of the accuracy of instrumental response.Ideally,if the haze of narrow-angle-scattering specimens (such as plastic films)is to be measured,narrow-angle-scattering glass standards should be used;7,8however,these are not known to be commercially available.In their absence,wide-angle-plastic standards 10may be used,but these are less sensitive to the size and centering of the annulus described by Billmeyer and Chen 6and Weidner and Hsia,9and particular attention should be paid to Note 1when only plastic haze standards are used.7.2Procedure :7.2.1Determine the following four readings:Reading DesignationSpecimen in PositionLight Trap in PositionReflectance Standard in PositionQuantity Represented T 1no no yes incident lightT 2yes no yes total light transmitted by specimenT 3no yes no light scattered by instru-mentT 4yesyesnolight scattered by instru-ment and specimen7.2.2Repeat readings for T 1,T 2,T 3,and T 4with additional specified positions of the specimen to determine uniformity.7.3Calculation 11:7.3.1Calculate total transmittance,T t (Note 5),equal to T 2/T 1.7.3.2Calculate diffuse transmittance,T d (Note 5),as fol-lows:T d 5@T 42T 3~T 2/T 1!#/T 1(1)7.3.3Calculate percent haze as follows:haze 5T d /T t 3100(2)N OTE 5—To obtain the greatest accuracy in luminous transmittance measurement when using a single-beam instrument,it is necessary to use a standard,calibrated with a double-beam instrument,because insertion of the sample in the single-beam instrument changes the efficiency of the sphere.This change may result in spuriously high readings for clear,colorless samples and significant errors for dark or highly saturated colors.In these cases,the photometer should be used as a comparison instrument with a standard of known transmittance similar to that of the specimen.For greatest accuracy of luminous transmittance measurement,compare the transmittance of the specimen with that of a calibrated standard of similar luminous transmittance.7.4Report :7.4.1Report the following data:7.4.1.1Source and identity of specimen,7.4.1.2Nominal thickness of specimen to the nearest 0.025mm,7.4.1.3Total luminous transmittance,T t ,to the nearest 0.1%(indicate the average when reporting average values and specify whether CIE Illuminant C or A is used),7.4.1.4Diffuse luminous transmittance,T d ,to the nearest 0.1%(indicate the average when reporting average values),and7.4.1.5Percent haze,to the nearest 0.1%(indicate the average when reporting average values).7.5Precision and Bias—Hazemeter :7.5.1Precision :7.5.1.1Table 1and Table 2are based on a round robin conducted in 1985,in accordance with Practice E 691,involv-ing six film materials tested by 11laboratories.In the round robin,each laboratory that measured a property made eight replicate measurements of the property for each of the six materials listed as 1to 6in Table 1and Table 2.7.5.1.2Table 3is based on a round robin conducted in 1991involving eight materials and six laboratories.This table can be directly compared to Table 4(Spectrophotometer).N OTE 6—Caution:The following explanations of r and R (7.5.1.3-7.5.1.7)are intended to present only a meaningful way of considering the approximate precision of this test method.The data in Tables 1-3should not be applied rigorously to acceptance or rejection of material,as those data are specific to the round robin and may not be representative of other9Highly reflective matte barium sulfate paint or pressed polytetrafluoroethylene powder are excellent for this purpose.See Practice E 259.10Calibrated plastic haze standards are available from BYK-Gardner,Inc.,2435Linden Lane,Silver Spring,MD 20910.11See Appendix X1for derivation offormulas.FIG.1Schematic of HazemeterTABLE 1Summary of 1985Procedure A (Hazemeter)Total HazeRound Robin Involving Eleven LaboratoriesMaterial Average S(r)S(R)r R 3 3.80.100.330.280.9418.70.180.420.50 1.18213.50.080.400.23 1.12418.00.270.610.76 1.72521.00.41 1.68 1.16 4.74626.50.351.130.983.19lots,conditions,materials,or ers of this test method should apply the principles outlined in Practice E 691to generate data specific to their laboratory and materials,or between specific laboratories.The principles of 7.5.1.3-7.5.1.7would then be valid for such data.7.5.1.3For the purpose of compiling summary statistics,a test result has been defined to be the average of three replicate measurements of a property for a material in a laboratory,as specified in this test method.Summary statistics are given in Tables 1-3.In each table,for the material indicated,S(r)is the pooled within-laboratory standard deviation of a test result,S(R)is the between-laboratory standard deviation of a test result,r =2.833S(r)(see 7.5.1.4),and R =2.833S(R)(see 7.5.1.5).7.5.1.4Repeatability —Two test results obtained within one laboratory shall be judged not equivalent if they differ by morethan the “r ”value for that material.“r ”is the interval representing the critical difference between two test results for the same material,obtained by the same operator using the same equipment on the same day in the same laboratory.7.5.1.5Reproducibility —Two test results obtained by dif-ferent laboratories shall be judged not equivalent if they differ by more than the “R ”value for that material.“R ”is the interval representing the critical difference between two test results for the same material,obtained by different operators using differ-ent equipment in different laboratories.7.5.1.6Judgments made as described in 7.5.1.3and 7.5.1.4will be correct in approximately 95%of such comparisons.7.5.1.7For further information,see Practice E 691.7.5.2Bias —Measurement biases cannot be determined since there are no accepted referee methods for determining these properties.8.Procedure B (Spectrophotometer)8.1Apparatus :8.1.1The instruments used for measurement shall meet the geometric and spectral requirement of this section.8.1.2The instrument shall be capable of computing from the spectral data the 1931CIE tristimulus values and related color coordinates for CIE standard Illuminant C or alterna-tively Illuminant A.8.1.3The instrument shall utilize a hemispherical optical measuring system,with an integrating sphere,in which the specimen can be placed flush against the sphere port.The surfaces of the interior of the integrating sphere,baffles,and reflectance standards shall be matte,of substantially equal reflectance and highly reflecting throughout the visible wave-lengths.8.1.4Two geometries can be used:unidirectional illumina-tion with diffuse viewing and diffuse illumination with unidi-rectional ing Geometry B the following apply:8.1.4.1Use an integrating sphere to illuminate the specimen diffusely;the sphere may be of any diameter as long as the total port areas do not exceed 4.0%of the internal reflecting area of the sphere.The specimen and light trap ports of the sphere shall be centered on the same great circle of the sphere,and there shall be at least 2.97rad (170°)of arc between their centers.The light trap port shall subtend an angle of 0.14rad (8°)at the center of the specimen port along the wowing beam.With the light trap in position,without specimen the axis of the viewing beam shall pass through the centers of the specimen and light trap ports.8.1.4.2View the specimen along an axis defined by a substantially unidirectional beam;the maximum angle that any ray of this beam may make with the beam axis shall not exceed 0.05rad (3°).This beam shall not be vignetted at either port of the sphere.8.1.4.3When the specimen is in place,the angle between the specimen normal and the line connecting the centers of the specimen and the light trap ports shall not exceed 0.14rad (8°).8.1.4.4With no specimen in place,the viewed area at the exit port shall be approximately circular,sharply defined concentric within the light trap port,leaving an annulus of 0.02360.002rad (1.360.01°)subtended at the specimen port.TABLE 2Summary of 1985Procedure A (Hazemeter)Luminous Transmittance Round Robin Involving Eleven LaboratoriesMaterial Average S(r)S(R)r R 283.60.25 1.210.69 3.42484.80.15 1.060.42 3.02186.40.08 1.080.22 3.06387.50.20 1.070.57 3.02688.50.14 2.100.38 5.93588.60.352.230.996.32TABLE 3Summary of 1991Procedure A (Hazemeter)Total HazeRound Robin Involving Six LaboratoriesMaterial Average S(r)S(R)r R LDPE A 0.580.0310.1330.0860.372B 1.890.0290.2160.0800.604C 2.080.0210.2000.0580.568PET D 2.690.0420.3130.1170.075E 5.740.0310.3950.086 1.106F 8.060.0490.5660.137 1.584G 12.680.0500.4900.140 1.372H28.570.0911.0420.2562.9918TABLE 4Summary of 1991Procedure B (Spectrophotometer)Total Haze Round Robin Involving Seven LaboratoriesMaterial Average S(r)A S(R)B r C R D LDPE A 0.550.0760.1860.2130.522B 1.770.0870.6580.244 1.019C 1.010.0420.3970.175 1.112PET D 2.510.1150.3310.3230.927E 5.050.0810.5960.227 1.669F 6.550.189 1.1380.305 3.186G 11.350.137 1.2890.385 3.610H25.450.1583.0200.4438.455AS r is the within laboratory standard deviation for the indicated material.It is obtained by pooling the within-laboratory standard deviations of the test results from all of the participating laboratories:S r 5@@~s 1!21~s 2!2...1~s n !2#/n #½BS R is the between laboratories reproducibility,expressed as standard devia-tion:S R 5@s r 21s L 2#½where:s L =standard deviation of laboratory means.Cr is the within-laboratory critical interval between two test results =2.83S r .DR is the between-laboratories critical interval between two test results =2.83S R.N OTE 7—Note 3and Note 4apply.It should be noted that it may be difficult,but is critical,to meet this requirement.8.1.5A light trap shall be provided that will completely absorb the beam when no specimen is present,or the instru-ment design shall obviate the need for a light trap.8.1.6A schematic drawing of a spectrophotometer with unidirectional illumination and diffuse viewing is shown in Fig.2.N OTE 8—It is strongly recommended that conformance to the intent of this test method be confirmed through use of properly calibrated haze standards due to the difficulty of confirming conformance to this test method when using a drill spectrophotometer.8.2Procedure —Follow the manufacturer’s instructions for the measurement of haze,and if none available,use Section 8.8.3Calculation —Most spectrophotometers are computer driven and values for luminous transmission and haze are automatically calculated.If values are not computed use calculation method in Section 9.8.4Report :8.4.1Report the following data:8.4.1.1Source and identity of specimen,8.4.1.2Nominal thickness of specimen,8.4.1.3Percent haze,to the nearest 0.1%(indicate the average when reporting average values),8.4.1.4Total luminous transmittance,T t ,to the nearest 0.1%(indicate the average when reporting average values and specify whether CIE Illuminant C or A is used)when specifi-cally requested,and8.4.1.5Diffuse luminous transmittance,T d ,to the nearest 0.1%(indicate the average when reporting average values)when specifically requested.8.5Precision and Bias :8.5.1Precision :8.5.1.1Precision data in Table 4is based on a round robin conducted in 1991involving eight materials and seven labo-ratories.For comparison purposes the same materials were measured on six regular hazemeters during the same round robin.The data from the regular hazemeter round robin is included in Table 3.N OTE 9—Caution:The following explanations of r and R (8.5.1.2-8.5.1.6)are intended to present only a meaningful way of considering the approximate precision of this test method.The data in Tables 1-4should not be applied rigorously to acceptance or rejection of material,as those data are specific to the round robin and may not be representative of other lots,conditions,materials,or ers of this test method should apply the principles outlined in Practice E 691to generate data specific to their laboratory and materials,or between specific laboratories.The principles of 8.5.1.2-8.5.1.6would then be valid for such data.8.5.1.2For the purpose of compiling summary statistics,a test result has been defined to be the average of three replicate measurements of a property for a material in a laboratory,as specified in this test method.Summary statistics are given in Table 4.In each table,for the material indicated,S(r)is the pooled within-laboratory standard deviation of a test result,S(R)is the between-laboratory standard deviation of a test result,r =2.833S(r)(see 8.5.1.3),and R =2.833S(R)(see 8.5.1.4).8.5.1.3Repeatability —In comparing two mean values of the same material,obtained by the same operator using the same equipment on the same day,the means should be judged not equivalent if they differ by more than the r value for that material.8.5.1.4Reproducibility —In comparing two mean values for the same material obtained by different operators using differ-ent equipment on different days,either in the same laboratory or in different laboratories,the means should be judged not equivalent if they differ by more than the R value for that material.8.5.1.5Judgments made as described in 8.5.1.3and 8.5.1.4will be correct in approximately 95%of such comparisons.8.5.1.6For further information,see Practice E 691.8.5.2Bias —Measurement biases cannot be determined since there are no accepted referee methods for determining these properties.9.Referee Procedure9.1In case of dispute,Procedure A—Hazemeter will be the referee procedure measured with a standard hazemeter.10.Keywords10.1haze;luminous transmittance;regular transmittance;transparentplasticsFIG.2Spectrophotometer With DiffuseIlluminationAPPENDIXES(Nonmandatory Information)X1.DERIV ATION OF FORMULAS FOR HAZEX1.1The derivation of the formula for haze for both procedures is as follows:X1.1.1Total luminous transmittance,T t,is calculated as follows:T t5T2/T1(X1.1)where:T2=total light transmitted by the specimen,andT1=incident light.X1.1.2If T3,the light scattered by the instrument,is zero, the diffuse luminous transmittance,T d,is calculated as follows:T d5T4/T1(X1.2)where:T4=light scattered by the instrument and specimen.X1.1.3If T3is greater than zero due to light scattered by the instrument,the total scattered light,T4,will be greater than the light scattered by the specimen by an amount proportional to T3 and equal to T3times T2/T1.The corrected amount of light scattered by the specimen will then be the following:T42T3~T2/T1!(X1.3) X1.1.4The diffuse luminous transmittance,T d,is then calculated as follows:T d5@T42T3~T2/T1!#/T1(X1.4) X1.1.5Percent haze is then calculated from the ratio of diffuse,T d,to total luminous transmittance,T t,as follows:haze,%5~T d/T t!3100(X1.5) 5@~T42T3~T2/T1!#/T14~T2/T1!#31005@~T42T3~T2/T1!#/T2!31005@~T4/T2!2~T3/T1!#3100X2.ALTERNATIVE HAZE(SHORTCUT)PROCEDUREX2.1Many commercial hazemeters have indicating sys-tems and a means of adjusting the light scattered by the instrument to zero and the total light transmitted by the specimen to100.For these instruments,the following is a shortcut method that can be used for determining haze.N OTE X2.1—This shortcut procedure may produce erroneous values for highly absorbing samples,or those measured in a stopped-down beam mode(as for Tabor abrasion haze).With such samples,instrument stray light may not be properly accounted for.It is recommended that in such situations a comparison be made of the standard procedure and the shortcut procedure using typical samples.In case of any disagreement,the standard procedure shall be considered to produce the correct values.X2.1.1With the hazemeter set to measure total transmit-tance,adjust the instrument output to read100.0.X2.1.2With the hazemeter set to measure light scattered by the instrument,adjust the instrument output to read0.0.X2.1.3With the hazemeter set to measure total transmit-tance,place the test specimen against the entrance port of the integrating sphere.X2.1.4Adjust the instrument output to read100.0.X2.1.5Set the instrument to measure light scattered by the specimen and record the reading as percent haze.ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentioned in this ers of this standard are expressly advised that determination of the validity of any such patent rights,and the risk of infringement of such rights,are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed everyfive years and if not revised,either reapproved or withdrawn.Your comments are invited either for revision of this standard or for additional standards and should be addressed to ASTM International Headquarters.Your comments will receive careful consideration at a meeting of the responsible technical committee,which you may attend.If you feel that your comments have not received a fair hearing you should make your views known to the ASTM Committee on Standards,at the address shown below.This standard is copyrighted by ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959, United States.Individual reprints(single or multiple copies)of this standard may be obtained by contacting ASTM at the above address or at610-832-9585(phone),610-832-9555(fax),or service@(e-mail);or through the ASTM website().。

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