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    BS EN ISO 13137-2013 Workplace atmospheres Pumps for personal sampling of chemical and biological agents Requirements and test methods《工作场所空气 化学和生物制剂个人采样泵 试验方法和要求》.pdf

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    BS EN ISO 13137-2013 Workplace atmospheres Pumps for personal sampling of chemical and biological agents Requirements and test methods《工作场所空气 化学和生物制剂个人采样泵 试验方法和要求》.pdf

    1、BSI Standards PublicationBS EN ISO 13137:2013Workplace atmospheres Pumps for personal samplingof chemical and biologicalagents Requirements andtest methodsBS EN ISO 13137:2013 BRITISH STANDARDNational forewordThis British Standard is the UK implementation of EN ISO 13137:2013. It supersedes BS EN 12

    2、32:1997 and BS EN 12919:1999 which are withdrawn.The UK participation in its preparation was entrusted to Technical Committee EH/2/2, Work place atmospheres.A list of organizations represented on this committee can be obtained on request to its secretary.This publication does not purport to include

    3、all the necessary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2013. Published by BSI Standards Limited 2013ISBN 978 0 580 69771 5 ICS 13.040.30; 23.080 Compliance with a British Standard cannot confer immunity from legal obligations.

    4、This British Standard was published under the authority of the Standards Policy and Strategy Committee on 31 October 2013.Amendments issued since publicationDate T e x t a f f e c t e dEUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN ISO 13137 October 2013 ICS 13.040.30 Supersedes EN 1232:1997,

    5、EN 12919:1999English Version Workplace atmospheres - Pumps for personal sampling of chemical and biological agents - Requirements and test methods (ISO 13137:2013) Air des lieux de travail - Pompes pour le prlvement individuel des agents chimiques et biologiques - Exigences et mthodes dessai (ISO 13

    6、137:2013) Arbeitsplatzatmosphre - Pumpen fr die personenbezogene Probenahme von chemischen und biologischen Arbeitsstoffen - Anforderungen und Prfverfahren (ISO 13137:2013) This European Standard was approved by CEN on 28 September 2013. CEN members are bound to comply with the CEN/CENELEC Internal

    7、Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN

    8、member. This European Standard exists in three official versions (English, French, German). A version in any other language made by translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the official version

    9、s. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Pol

    10、and, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2013 CEN All rights of exploitation

    11、 in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN ISO 13137:2013: EBS EN ISO 13137:2013EN ISO 13137:2013 (E) 3 Foreword This document (EN ISO 13137:2013) has been prepared by Technical Committee ISO/TC 146 “Air quality“ in collaboration with Technical Committee C

    12、EN/TC 137 “Assessment of workplace exposure to chemical and biological agents” the secretariat of which is held by DIN. This European Standard shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by April 2014, and conflicting

    13、national standards shall be withdrawn at the latest by April 2014. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document super

    14、sedes EN 1232:1997, EN 12919:1999. According to the CEN-CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav

    15、 Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. Endorsement notice The text of ISO 13137:2013 has be

    16、en approved by CEN as EN ISO 13137:2013 without any modification. BS EN ISO 13137:2013ISO 13137:2013(E) ISO 2013 All rights reserved iiiContents PageForeword vIntroduction vi1 Scope . 12 Normative references 13 Terms and definitions . 14 Types of pump . 35 Requirements 35.1 Features . 35.2 Mass 35.3

    17、 Design safety . 45.4 Operating time. 45.5 Start-up and long-term performance 45.6 Short-term interruption of air flow . 45.7 Temperature dependence 45.8 Mechanical strength . 55.9 Pulsation of flow rate (for type P pumps only) . 55.10 Flow rate stability under increasing pressure drop . 55.11 Timer

    18、 accuracy 55.12 Electromagnetic compatibility 55.13 Explosion hazard . 66 Test conditions . 66.1 Number of test objects . 66.2 Test instruments 66.3 Preconditioning and sequence of tests 76.4 Adjustment of volume flow rate and pressure drop . 76.5 Test set-up and performance 77 Test methods . 87.1 F

    19、eatures . 87.2 Mass 87.3 Design safety . 87.4 Operating time. 87.5 Start-up and long-term performance 87.6 Short-term interruption of air flow . 97.7 Temperature dependence. 107.8 Mechanical strength 117.9 Pulsation of flow rate (for type P pumps only) 127.10 Flow rate stability under increasing pre

    20、ssure drop 147.11 Timer accuracy. 157.12 Electromagnetic compatibility . 157.13 Explosion hazard 158 Test report 159 Instructions for use 1610 Charger 1610.1 Requirements 1610.2 Testing .1611 Marking .17Annex A (informative) Types of pump mechanism and control system .18Annex B (informative) Interna

    21、l sensors of sampling pumps .21BS EN ISO 13137:2013ISO 13137:2013(E)iv ISO 2013 All rights reservedAnnex C (informative) User tests for pumps and flow meters 23Annex D (informative) Pressure drop due to collection substrates 26Annex E (informative) Test instruments .30Bibliography .31BS EN ISO 13137

    22、:2013ISO 13137:2013(E)ForewordISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees. Each member body interested in a

    23、subject for which a technical committee has been established has the right to be represented on that committee. International organizations, governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the International Electrotechnical Commission

    24、 (IEC) on all matters of electrotechnical standardization.The procedures used to develop this document and those intended for its further maintenance are described in the ISO/IEC Directives, Part 1. In particular the different approval criteria needed for the different types of ISO documents should

    25、be noted. This document was drafted in accordance with the editorial rules of the ISO/IEC Directives, Part 2, www.iso.org/directives.Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. ISO shall not be held responsible for identifying

    26、 any or all such patent rights. Details of any patent rights identified during the development of the document will be in the Introduction and/or on the ISO list of patent declarations received, www.iso.org/patents.Any trade name used in this document is information given for the convenience of user

    27、s and does not constitute an endorsement.The committee responsible for this document is ISO/TC 146, Air quality, Subcommittee SC 2, Workplace atmospheres. ISO 2013 All rights reserved vBS EN ISO 13137:2013ISO 13137:2013(E)IntroductionMany different methods are used to determine the concentration of

    28、chemical and biological agents in workplace air. Many of these methods involve the use of a pump and sampler connected by a flexible tube. Air is drawn through the sampler and chemical and biological agents are trapped, e.g. on a filter, sorbent tube or long-term detector tube, or in a gas washing b

    29、ottle. In personal sampling, the pump and sampler are attached to the worker so as to collect chemical and biological agents in the breathing zone.The volume of air drawn by the pump during the sampling period is one of the quantities in the calculation of the concentration of the chemical and biolo

    30、gical agents in air. Therefore, the volume of air sampled should be determined accurately and, in order to facilitate this, the flow rate should be maintained within acceptable limits throughout the sampling period. For particle size selective sampling, the short-term fluctuation of the flow rate sh

    31、ould also be maintained within acceptable limits in order to ensure that the sampler exhibits the required collection characteristics.EN 4821specifies general performance criteria for methods for measuring the concentration of chemical and biological agents in workplace air. These performance criter

    32、ia include maximum values of expanded uncertainty that are not to be exceeded under prescribed laboratory conditions. In addition, the performance criteria should also be met under a wider variety of environmental influences, representative of workplace conditions. The contribution of the sampling p

    33、ump to measurement uncertainty should be kept to a minimum.This International Standard is intended to enable manufacturers and users of personal sampling pumps to adopt a consistent approach to, and provide a framework for, the assessment of the specified performance criteria. Manufacturers are urge

    34、d to ensure that pumps meet the requirements laid down in this International Standard, including environmental influences which can be expected to affect performance.vi ISO 2013 All rights reservedBS EN ISO 13137:2013Workplace atmospheres Pumps for personal sampling of chemical and biological agents

    35、 Requirements and test methods1 ScopeThis International Standard specifies performance requirements for battery powered pumps used for personal sampling of chemical and biological agents in workplace air. It also specifies test methods in order to determine the performance characteristics of such pu

    36、mps under prescribed laboratory conditions.This International Standard is applicable to battery powered pumps having a nominal volume flow rate above 10 ml min1, as used with combinations of sampler and collection substrate for sampling of gases, vapours, dusts, fumes, mists and fibres.This Internat

    37、ional Standard is primarily intended for flow-controlled pumps.2 Normative referencesThe following referenced documents, in whole or in part, are normatively referenced in this document and are indispensable for its application. For dated references, only the edition cited applies. For undated refer

    38、ences, the latest edition of the referenced document (including any amendments) applies.IEC 60079-0, Explosive atmospheres Part 0: Equipment General requirementsIEC 61000-6-1, Electromagnetic compatibility (EMC) Part 6-1: Generic standards Immunity for residential, commercial and light-industrial en

    39、vironmentsIEC 61000-6-3, Electromagnetic compatibility (EMC) Part 6-3: Generic standards Emission standard for residential, commercial and light-industrial environments3 Terms and definitionsFor the purposes of this document, the following terms and definitions apply.3.1biological agentbacteria, vir

    40、uses, fungi and other micro-organisms or parts of them and their associated toxins, including those which have been genetically modified, cell cultures or endoparasites which are potentially hazardous to human healthNote 1 to entry: Dusts of organic origin, e.g. pollen, flour dust and wood dust, are

    41、 not considered to be biological agents and are therefore not covered by this definition.SOURCE: EN 1540:2011,2definition 2.1.13.2chemical agentany chemical element or compound on its own or admixed as it occurs in the natural state or as produced, used, or released, including release as waste, by a

    42、ny work activity, whether or not produced intentionally and whether or not placed on the marketSOURCE: EN 1540:2011,2definition 2.1.2INTERNATIONAL STANDARD ISO 13137:2013(E) ISO 2013 All rights reserved 1BS EN ISO 13137:2013ISO 13137:2013(E)3.3airborne particlesfine matter, in solid or liquid form,

    43、dispersed in airNote 1 to entry: Smoke, fume, mist and fog consist of airborne particles.SOURCE: EN 1540:2011,2definition 2.2.33.4air samplersamplerdevice for separating chemical and/or biological agents from the surrounding airNote 1 to entry: Air samplers are generally designed for a particular pu

    44、rpose, e.g. for sampling gases and vapours or for sampling airborne particles.SOURCE: EN 1540:2011,2definition 3.2.1, modified synonyms placed on separate lines3.5personal samplersampler, attached to a person, that collects gases, vapours or airborne particles in the breathing zone to determine expo

    45、sure to chemical and/or biological agentsSOURCE: EN 1540:2011,2definition 3.2.23.6personal samplingprocess of (air) sampling carried out using a personal samplerSOURCE: EN 1540:2011,2definition 3.3.33.7breathing zonespace around the nose and mouth from which breath is takenNote 1 to entry: Technical

    46、ly the breathing zone corresponds to a hemisphere (generally accepted to be 30 cm in radius) extending in front of the human face, centred on the midpoint of a line joining the ears. The base of the hemisphere is a plane through this line, the top of the head and the larynx. This technical descripti

    47、on is not applicable when respiratory protective equipment is used.SOURCE: EN 1540:2011,2definition 2.4.53.8sorbent tubedevice, usually made of metal or glass, containing a collection substrate such as a sorbent or a support impregnated with reagentNote 1 to entry: Some sorbent tubes are intended fo

    48、r use as active samplers and some as passive samplers.SOURCE: EN 1540:2011,2definition 3.2.53.9pressure dropdifference between ambient pressure and the pressure at the inlet of the pump, for a constant volume flow rate settingNote 1 to entry: The pressure drop, sometimes referred to as back pressure

    49、, is measured across the sampler, the collection substrate and the tubing.3.10flow-controlled pumppump with nominally constant flow rate provided by an automatic flow control system2 ISO 2013 All rights reservedBS EN ISO 13137:2013ISO 13137:2013(E)3.11nominal flow rate rangerange of volume flow rate values, adjustable at the pump, at which the manufacturer claims that the pump can operate at a constant flow rate up to the maximum value of the required pressure drop range for the operating time3.12operating timeper


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