车辆内部零件和材料检测

GB/T 3883.1-2014手持式、可移式电动工具和园林工具的安全 第1部分:通用要求

GB 3883的本部分涉及电动机或电磁铁驱动的:--手持式电动工具(第2部分);--可移式电动工具(第3部分);--园林工具(第4部分)。以下简称“工具”。交流单相或直流工具的额定电压不大于250 V,交流三相工具的额定电压不大于440 V。大额定输入功率不超过3 700 W。本部分涉及人们在正常操作以及合理可预见的使用工具时遇到的由工具引发的危险。带电加热元件的工具属本部分范围。这些加热元件的要求在GB 4706的相关部分中规定。对于不与电网隔离、且基本绝缘由不按工具额定电压设计的电动机,其要求在附录B中规定。对于由可充电电池供电的电动机驱动或电磁铁驱动的工具以及用于这些工具的电池包,其要求在附录K中规定。对于能直接接在市电或非隔离电源上操作和/或充电的这类工具,其要求在附录L中规定。不用对工具自身作任何改造便能够安装到一个支架或工作台当作固定式工具使用的手持式电动工具属于本部分范围,由第3部分来规定。本部分不适用于:--在爆炸性环境(尘埃、蒸汽或气体)中使用的工具;--制备和加工食品用工具;--医疗用工具;--与化妆品和药品一起使用的工具;--加热工具;--电动机驱动的家用或类似用途电器;--工业机床用电气设备;--用来制作模型的由低压变压器驱动的小型台式工具,如制作遥控飞机模型或汽车模型等。

GB/T 19678.1-2018使用说明的编制 构成、内容和表示方法 第1部分:通则和详细要求

GB/T 19678的本部分规定了设计和编写各类使用说明的一般原则和详细要求。使用说明对于产品的用户来说非常有必要或有用。产品范围小到一罐油漆，大到大型或非常复杂的产品，比如大型工业成套设备或建筑。本部分适用于参与使用说明编制工作的各方，例如：供方、技术文档写作者、插图作者、软件设计者、译者或从事构思和起草说明书工作的其他人员。GB/T 19678的本部分未规定需要与产品共同交付的文件的固定数量，因为本部分适用于所有类型的产品，所需文件数量将取决于产品的性质、其复杂性和预期用户的技能。

GB/T 29334-2012用于非石油基液压制动液的汽车液压制动缸用的弹性体皮碗和密封圈

本标准规定了用于非石油基液压制动液的汽车液压制动缸用弹性体皮碗和双唇密封圈(以下统称为密封件)的术语和定义、一般要求、成品的要求、试验程序、检验规则、标志、包装、运输和贮存。本标准适用于鼓式制动器制动缸用直径不大于60 mm的橡胶模制密封件。本标准不适用于盘式制动器用弹性体密封件。

GB 51062-2014煤矿设备安装工程施工规范

本规范适用于煤矿建设及生产系统设备安装工程的施工。

MT 5010-1995煤矿安装工程质量检验评定标准

本标准适用于煤矿矿井及选煤厂的工业设备、钢结构井架、井筒装备、工作压力小于和等于10MPa的工业管道、小于和等于110kV的电气装置、通信、集控和架空索道等安装工程的质量检验评定。本标准主要是根据颁发的有关技术标准和施工验收规范并参照行业有关规范、标准等编制的。本标准未包括的工程项目及设备,建设单位可组织设计、施工单位按照本标准的制定原则,根据设计文件及设备出厂技术文件的要求自行补充临时标准,经省、市、自治区煤炭主管部门批准后执行,并报煤炭工业部备案。

ISO 12219-3-2012公路车辆内空气.第3部分:来自车辆内装品和材料的挥发性有机化合物释放测定筛选法.微尺度室法

This part of ISO 12219 specifies a fast, qualitative and\nsemiquantitative screening method for vapour-phase organic\ncompounds (volatile and some semi-volatile) released from vehicle\ntrim materials under simulated realuse conditions using micro-scale\ntest chambers. This method is intended for evaluating new car\ninterior trim components but can, in principle, also be applied to\nused car components.\nTarget analytes include VOCs (conventionally defined as organic\ncompounds in the volatility range of n-hexane to n-hexadecane) and\nvolatile carbonyl compounds such as formaldehyde. The specified\nanalytical procedure for VOCs is ISO 16000-6 and for formaldehyde\nand some other light carbonyl compounds is ISO 16000-3.\nNOTE 1 Some compounds more volatile than n-hexane and less\nvolatile than n-hexadecane can also be analysed (for more\ninformation, see: ISO 16000-6:2011, Annex D; ISO 16017-1;[11] and\nAnnex E).\nNOTE 2 For dry, homogeneous materials, results from tests of\nvolatile organic emissions ca

ISO 12219-4-2013道路车辆内空气.第4部分:来自车辆内装品和材料的挥发性有机化合物释放的测定方法.小室法

This part of ISO 12219 specifies a qualitative and quantitative\nanalytical method for vapour-phase organic compounds (volatile and\nsome semi-volatile) released from car trim materials under\nsimulated real use conditions using small emission test chambers\n(small chamber). Small chambers are intended to provide a transfer\nfunction to vehicle level emissions. This method is intended for\nevaluating new car interior trim components but can, in principle,\nbe applied to used car components.\nTarget compounds include VOCs (conventionally defined as organic\ncompounds in the volatility range n-hexane to\nn-hexadecane) and volatile carbonyl compounds such as formaldehyde.\nThe specified analytical procedure for VOCs is ISO 16000 6 and for\nformaldehyde and some other light carbonyl compounds is ISO 16000\n3.\nNOTE Compounds more volatile than n-hexane and less\nvolatile than n-hexadecane can also be analysed (see ISO\n16000-6:2011, Annex D, and ISO 16017-1^[8]for more\ninformat

EN 1991-1-6-2005欧洲法规1:对建筑物的作用.一般作用.实行中的作用.合并勘误表2008年7月［代替:CEN ENV 1991-2-6］

(1) EN 1991-1-6 provides principles and general rules for the determination of actions which should be taken into

DIN 3386-2012大工作压力小于或等于5 bar的空气过滤器.试验和要求

The available standard regulates requirements and examinations for gasfilters up to a nominal size of including DN 250, which operat with gases of DVGW-Arbeitsblatt G 260 (without LPG at liquid phase) at a maximum working pressure of 5 bar.

DIN EN 9102-2016航空航天系列.质量体系.重要部件的检验要求.德文和英文版本EN 9102-2015

This European Standard establishes the baseline requirements for performing and documenting FAI. Should there be a conflict between the requirements of this European Standard and applicable statutory or regulatory requirements, the applicable statutory or regulatory requirements shall take precedence. The primary purpose of FAI is to validate that product realization processes are capable of producing parts and assemblies that meet engineering and design requirements. A well-planned and executed FAI will provide objective evidence the manufacturer's processes can produce compliant product and that they have understood and incorporated associated requirements. FAI will: - Provide confidence that the product realization processes are capable of producing conforming product. - Demonstrate that the manufacturers and processors of the product have an understanding of the associated requirements. - Provide objective evidence of process capability. - Reduce potential risks associated with production start-up and/or process changes. - Provide assurance of product conformance at the start of production and after changes outlined in this European Standard. An FAI is intended to: - Reduce future escapes, risks, and total costs. - Help ensure safety of flight. - Improve quality, delivery, and customer satisfaction. - Reduce costs and production delays associated with product nonconformances. - Identify product realization processes that are not capable of producing conforming product, and initiate and/or validate corrective actions. This European Standard applies to organizations that are responsible for producing the design characteristics of the product (i.e., product realization). The organization shall flow down the requirements of this European Standard to suppliers or processors who produce design characteristics. This European Standard applies to assemblies, sub-assemblies, and detail parts including castings, forgings, and modifications to standard catalogue or Commerci

DIN EN ISO 16000-19-2014室内空气. 第19部分:霉菌取样策略 (ISO 16000-19-2012);德文版本EN ISO 16000-19-2014

Mould spores and metabolites can be inhaled via the air and cause allergic and irritating reactions and/or complex symptoms in humans. Increased concentrations of these compounds are considered a potential health risk. Moreover, mould growth may be associated with severe odour nuisances. This part of EN ISO 16000 provides assistance for the sampling strategy for suitable sampling and analysis methods together with a description of the applicability and the interpretation of the measurement results to maximize the comparability of the measured data obtained for a given measurement objective. Details on field inspections by qualified professionals which have to take place prior to any microbiological measurement are described. Depending on the analysis method mould spores are determined individually or as spore aggregate. Materials, indoor air and house dust will not only contain culturable but also non-culturable mould spores, some of which may have the same allergenic and toxic effects as culturable spores. For this reason, techniques have been developed which allow the microscopic determination of both culturable and non-culturable moulds. The sampling methods employed for detection of moulds are determined by the objective of the investigation (DIN ISO 16000-16 \"Filtration\" or DIN ISO 16000-18 \"Impaction\"). Depending on the sampling method, the moulds will suffer a sampling stress during sample collection and preparation, which may lead to their drying-out or dying. Mould detection and differentiation are performed either after cultivation based on morphological criteria, biochemical reactions and/or molecular techniques or by direct microscopic examination (DIN ISO 16000-17).

DIN EN ISO 16000-26-2012室内空气.第26部分:二氧化碳取样策略(CO2)(ISO 16000-26-2012).德文版本EN ISO 16000-26-2012

This part of ISO 16000 specifies the planning of carbon dioxide indoor pollution measurements. In the case of indoor air measurements, the careful planning of sampling and the entire measurement strategy are of particular significance since the result of the measurement may have far-reaching consequences, for example, with regard to ascertaining the need for remedial action or the success of such an action. An inappropriate measurement strategy may lead to misrepresentation of the true conditions or, worse, to erroneous results. This part of ISO 16000 is intended to be a link between Part 1 of ISO 16000, \"General Aspects of Sampling Strategy\", and the analytical procedures. Before indoor air measurements are carried out, the purpose of the measurement shall be clearly defined. In the case of determination of carbon dioxide, the following objectives are chiefly of interest and are dealt with in detail: - Investigating compliance with a guide value - Investigating the ventilation situation in a room By means of the measured value the ventilation rate needed can be used as a criterion of good air quality indoors and for calculating the design of room conditioning systems for ventilating indoor areas. Examples for calculations are presented.

DIN EN ISO 16000-32-2014室内空气. 第32部分: 对出现污染物建筑物的调查 (ISO 16000-32-2014); 德文版本EN ISO 16000-32-2014

This part of ISO 16000 specifies the requirements for investigating buildings for the presence of pollutants or other harmful factors, as basis for a subsequent sampling of suspect areas and determining the quantity and type of pollutant, which are described in other parts of ISO 16000. The results of the investigation provide the basis for assessing the building with regard to utilisation, remediation or demolition. An assessment with regard to utilisation may include hygiene and comfort parameters (e. g. for \"Building Passports\"). In specific circumstances it may be expedient to to assess the indoor air quality in order to undertake an investigation. The following objectives can be achieved: - to provide instructions for a structured approach, - to gather data and information as the basis for a more detailed assessment, - to assist in the compilation of a pollutant register, - to provide legal certainty for the client and the provider.