洁净室服装检测

GB/T 24249-2009防静电洁净织物

本标准规定了防静电洁净织物的技术要求、试验方法、检验规则、标志、包装、运输及贮存。本标准适用于在电子、半导体、医药、食品等行业的洁净室及相关受控环境使用的，用以制成洁净室服装、帽子、手套、鞋套等产品的织物。

GB/T 24579-2009酸浸取.原子吸收光谱法测定多晶硅表面金属污染物

1. 1本标准规定了用酸从多晶硅块表面浸取金属杂质，并用石墨炉原子吸收定量检测多晶硅块表面上的痕量金属杂质分析方法。1.2本标准适用于碱金属、碱土金属和第一系列过渡元素如钠、铝、铁、铬、镍、锌的检测。1.3本标准适用于各种棒、块、粒、片形多晶或单晶硅表面金属污染物的检测。由于块、片或粒形状不规则，面积很难准确测定，根据样品重量计算结果。使用的样品重量为50 g～300 g，检测限为0.01 ng/g。1.4酸的强度、组成、温度和浸取时间决定着表面腐蚀深度和表面污染物的浸取效率。在这个试验方法中腐蚀掉的样品重量小于样品重量的1%。1.5该试验方法提出了一种特定的样品尺寸、酸组成、腐蚀周期、试验环境和仪器方案，这些参数可以调整，但可能影响金属的回收效率及滞留量。该方法适用于重量为25 g～5 000 g的样品的测定，为达到仲裁的目的，该试验方法规定样品重量为300 g。该试验方法在干扰和结果的偏差方面做了详细说明。1.6该试验方法详细说明了用于分析酸提取痕量金属含量的石墨炉原子吸收光谱法的使用。也可使用灵敏度相当的其他仪器如电感耦合等离子体/质谱仪。1.7方法的检测限和偏差取决于酸提取过程的效率、样品尺寸、方法干扰、每个元素的吸收谱及仪器灵敏度、背景和空白值。1.8该方法是用热酸来腐蚀掉硅表面，腐蚀剂是有害的，操作必须在通风橱中进行，整个过程中必须非常小心。氢氟酸溶液非常危险，不熟悉专门防护措施的人不能使用。

GB/T 25915.5-2010洁净室及相关受控环境 第5部分：运行

GB/T 25915的本部分规定了洁净室运行的基本要求，供准备使用并运行洁净室的人员使用。本部分内容未涉及与污染控制有直接关联的安全问题，相关问题应遵守和地方的安全法规。本部分涉及生产各类产品的各个级别的洁净室。应用范围广泛，但未涉及各个行业的特定要求。本部分未包括洁净室的常规监测方法和规划的细节，关于粒子的监测参见GB/T 25915.2和GB/T 25915.3，微生物的监测参见GB/T 25916.1和GB/T 25916.2。

FZ/T 80012-2012洁净室服装.点对点电阻检测方法

本标准规定了洁净室服装点对点电阻的检测方法。其中包括术语和定义、检测原理、检测装置、检测环境、检测程序、结果报告。本标准适用于洁净室服装的检测。在电子、医药、航空航天、精密仪器等行业使用的无洁净性能要求的防静电服装也可按照本标准规定的方法检测点对点电阻。

FZ/T 80013-2012洁净室服装.易脱落大微粒检测方法

本标准规定了洁净室服装易脱落大微粒的检测方法，其中包括：术语和定义、检测项目、检测原理、检测条件、检测操作、数据处理、结果报告等。本标准适用于纺织机织物制作而成的洁净室服装，非织造布制作的洁净室服装也可参照进行。本标准不适用于非透气性材料在座的洁净室服装。

FZ/T 80014-2012洁净室服装.通用技术规范

本标准规定了洁净室服装的通用技术要求、试验方法、检验规则和包装、标识、运输及贮存等全部技术特征。本标准适用于在电子、航空、航天、精密仪器、医药等行业的洁净室及相关受控环境使用的工作服装。特定行业对于洁净室服装的特殊要求，如微生物性能、硅油含量、离子含量等，应参照相关行业的专门规定。本标准不适用于不透气型材料制作的洁净室服装。

ASTM F51/F51M-2020洁净室服装内外颗粒污染物尺寸测定及计数的试验方法

1.1 This test method covers the determination of detachable particulate contaminant 5 μm or larger, in and on the fabric of clean room garments. 1.2 This test method does not apply to nonporous fabrics such as Tyvek (trademarked) or Gortex (trademarked). It only applies to fabrics that are porous such as cotton or polyester. 1.3 This test method provides not only the traditional optical microscopic analysis but also a size distribution and surface obscuration analysis for particles on a fine-textured membrane filter or in a tape lift sample. It utilizes transmitted illumination to render all particles darker than the background for gray level detection. Particles collected on opaque plates must be transferred to a suitable membrane filter. 1.4 Units—The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined. 1.5 This standard may involve hazardous materials, operations, and equipment. This 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 appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

EN ISO 14644-4-2001洁净室和相关控制环境.第4部分:设计,建造和启用 ISO 14644-4-2001

This part of ISO 14644 specifies requirements for the design and construction of cleanroom installations but does not prescribe specific technological or contractual means to meet these requirements. It is intended for use by purchasers, suppliers and designers of cleanroom installations and provides a checklist of important parameters of performance. Construction guidance is provided, including requirements for start-up and qualification. Basic elements of design and construction needed to ensure continued satisfactory operation are identified through the consideration of relevant aspects of operation and maintenance.NOTE Further guidance in respect of the

DIN EN 16602-70-58-2015航天产品保证. 洁净室的生物负荷控制; 英文版本EN 16602-70-58-2015

This standard establishes the principles and basic methodology for microbiological control of cleanrooms and associated controlled environments with planetary protection constraints. This standard does not address: the microbiological contamination control of spaceflight hardware; molecular contamination control. Reference is made to other documents; fire and safety regulations; for these, see regulatory requirements and other national or local documentation. This standard does not lay down the methods for determining the microbiological and particulate cleanliness levels. Reference is made to other documents. This standard may be tailored for the specific characteristic and constrains of a space project in conformance with ECSS-S-ST-00.

DIN EN ISO 13408-1-2015保健品无菌加工.第1部分:通用要求(ISO 13408-1-2008,包含Amd 1-2013).德文版本EN ISO 13408-1-2015

ISO 13408-1:2008 specifies the general requirements for, and offers guidance on, processes, programmes and procedures for development, validation and routine control of the manufacturing process for aseptically-processed health care products.ISO 13408-1:2008 includes requirements and guidance relative to the overall topic of aseptic processing. Specific requirements and guidance on various specialized processes and methods related to filtration, lyophilization, clean-in place (CIP) technologies, sterilization in place (SIP) and isolator systems are given in other parts of ISO 13408.

BS EN ISO 14644-4-2001洁净室和相关控制环境.设计,建造和启动

This part of ISO 14644 specifies requirements for the design and construction of cleanroom installations but does not prescribe specific technological or contractual means to meet these requirements. It is intended for use by purchasers, suppliers and designers of cleanroom installations and provides a checklist of important parameters of performance. Construction guidance is provided, including requirements for start-up and qualification. Basic elements of design and construction needed to ensure continued satisfactory operation are identified through the consideration of relevant aspects of operation and maintenance.\nNOTE Further guidance in respect of the above requirements is given in annexes A to H. Other parts of ISO 14644 may provide complementary information.\nApplication of this part of ISO 14644 is restricted in the following:\n— user requirements are represented by purchaser or specifier;\n— specific processes to be accommodated in the cleanroom installation are not specified;\n— fire and safety regulations are not considered specifically; the appropriate national and local requirements should be respected;\n— process media and utility services are only considered with respect to their routing between and in the different zones of cleanliness;\n— regarding initial operation and maintenance, only cleanroom construction-specific requirements are considered.