BS ISO 22241-2-2006 Diesel engines - NOx reduction agent AUS 32 - Test methods《柴油发动机 NOx还原剂AUS 32 试验方法》.pdf

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1、BRITISH STANDARDBS ISO 22241-2:2006Incorporating corrigendum January 2008Diesel engines NOx reduction agent AUS 32 Part 2: Test methodsICS 43.060.40g49g50g3g38g50g51g60g44g49g42g3g58g44g55g43g50g56g55g3g37g54g44g3g51g40g53g48g44g54g54g44g50g49g3g40g59g38g40g51g55g3g36g54g3g51g40g53g48g44g55g55g40g39

2、g3g37g60g3g38g50g51g60g53g44g42g43g55g3g47g36g58BS ISO 22241-2:2006This British Standard was published under the authority of the Standards Policy and Strategy Committee on 30 November 2006 BSI 2008ISBN 978 0 580 61747 8National forewordThis British Standard is the UK implementation of ISO 22241-2:2

3、006, incorporating corrigendum January 2008. It supersedes DD ISO/PAS 22241-2:2005 which is withdrawn.The UK participation in its preparation was entrusted to Technical Committee MCE/22, Engines for road vehicles.A list of organizations represented on this committee can be obtained on request to its

4、 secretary.This publication does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application.Compliance with a British Standard cannot confer immunity from legal obligations.Amendments/corrigenda issued since publicationDate Comments30 April 2

5、008 Implementation of ISO corrigendum January 2008 (correcting paragraph 2 of D.5.4)Reference numberISO 22241-2:2006(E)INTERNATIONAL STANDARD ISO22241-2First edition2006-10-15Diesel engines NOx reduction agent AUS 32 Part 2: Test methods Moteurs diesel Agent AUS 32 de rduction des NOx Partie 2: Mtho

6、des dessai BS ISO 22241-2:2006ii iiiContents Page Foreword iv 1 Scope . 1 2 Normative references . 1 3 Specifications 1 4 Sampling 1 5 Precision and dispute. 2 Annex A (normative) Sampling. 3 Annex B (normative) Determination of urea content by total nitrogen 5 Annex C (normative) Refractive index a

7、nd determination of urea content by refractive index. 9 Annex D (normative) Determination of alkalinity 13 Annex E (normative) Determination of biuret content . 16 Annex F (normative) Determination of aldehyde content 21 Annex G (normative) Determination of insoluble matter content by gravimetric me

8、thod . 25 Annex H (normative) Determination of phosphate content by photometric method 28 Annex I (normative) Determination of trace element content (Al, Ca, Cr, Cu, Fe, K, Mg, Na, Ni, Zn) by ICP-OES method 34 Annex J (normative) Determination of identity by FTIR spectrometry method. 40 Annex K (inf

9、ormative) Precision of test methods . 42 Bibliography . 43 BS ISO 22241-2:2006iv Foreword ISO (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

10、 ISO technical committees. Each member body interested in a 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 collaborate

11、s closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization. International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2. The main task of technical committees is to prepare International Standards

12、. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publication as an International Standard requires approval by at least 75 % of the member bodies casting a vote. Attention is drawn to the possibility that some of the elements of this

13、 document may be the subject of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. ISO 22241-2 was prepared by Technical Committee ISO/TC 22, Road vehicles, Subcommittee SC 5, Engine tests. This first edition cancels and replaces ISO/PAS 22241-2:2005, whi

14、ch has been technically revised. ISO 22241 consists of the following parts, under the general title Diesel engines NOx reduction agent AUS 32: Part 1: Quality requirements Part 2: Test methods The following parts are under preparation: Part 3: Packaging, transportation and storage Part 4: Refilling

15、interface Annexes A to J form a normative part of this International Standard. Annex K is for information only. BS ISO 22241-2:20061Diesel engines NOx reduction agent AUS 32 Part 2: Test methods 1 Scope This part of ISO 22241 specifies test methods required for determination of the quality character

16、istics of the NOx reduction agent AUS 32 (aqueous urea solution) specified in ISO 22241-1. In the remaining parts of ISO 22241, the term “NOx reduction agent AUS 32” will be abbreviated to “AUS 32”. 2 Normative references The following referenced documents are indispensable for the application of th

17、is document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. ISO 22241-1, Diesel engines NOx reduction agent AUS 32 Part 1: Quality requirements ISO 3675, Crude petroleum and liquid petrol

18、eum products Laboratory determination of density Hydrometer method ISO 3696, Water for analytical laboratory use Specification and test methods ISO 4259, Petroleum products Determination and application of precision data in relation to methods of test ISO 12185, Crude petroleum and petroleum product

19、s Determination of density Oscillating U-tube method 3 Specifications Compliance with the limits specified in Table 1 of ISO 22241-1 shall be determined by the test methods specified in Annexes B through J of this part of ISO 22241. Determination of the density shall be conducted in accordance with

20、ISO 3675 or ISO 12185. NOTE For the purposes of this International Standard, the terms “% (m/m)” and “% (V/V)” are used to represent the mass fraction and the volume fraction of a material respectively. 4 Sampling Samples shall be taken in accordance with Annex A. BS ISO 22241-2:20062 5 Precision an

21、d dispute 5.1 General All test methods referred to in this part of ISO 22241 include a precision statement according to ISO 4259. In cases of dispute, the procedures described in ISO 4259 shall be used for resolving the dispute, and interpretation of the results based on the test method precision sh

22、all be used. The precision of the test method, as determined by statistical examination in accordance with ISO 4259, is specified in each annex. Additionally, this information is summarized in Annex K for all test methods for the convenience of the user of this part of ISO 22241. The statistical sig

23、nificance of the precision quoted in this part of ISO 22241 is generically defined in 5.2 and 5.3, in which the “xx (unit)” stands for the repeatability and reproducibility in question. 5.2 Repeatability, r The difference between two test results obtained by the same operator with the same apparatus

24、 under constant operating conditions on identical test material would, in the long run, in the normal and correct operation of the test method, exceed xx (unit) in only one case in 20. 5.3 Reproducibility, R The difference between two single and independent test results obtained by different operato

25、rs working in different laboratories on identical test material would, in the long run, in the normal and correct operation of the test method, exceed xx (unit) in only one case in 20. BS ISO 22241-2:20063Annex A (normative) Sampling A.1 General The sampling method specified in this annex is valid f

26、or each sampling of AUS 32 throughout the supply chain after the shipment from the manufacturers site to the AUS 32 containers of the vehicles. A.2 Principle The limits for the quality characteristics of AUS 32, which are specified in ISO 22241-1, are the representative analytical results that can o

27、nly be obtained when the sample is protected from any contamination before the analysis. Therefore, suitable bottles shall be used for sampling, which do not contaminate the sample, especially regarding the trace elements, and which minimize the risk of algae or bacteria growth. NOTE The sampling me

28、thod specified in this annex is based on ISO 5667-2 and ISO 5667-3. A.3 Possible contaminants During the sampling process, foreign matter may lead to contamination of the sample. Under realistic conditions, the following sources of contamination will pose a major hazard: residues of process aids use

29、d for the production of the sampling bottles; contaminants which have been deposited in the empty bottles during the time they are stored empty; contaminants from the air, i.e. dust or any foreign matter from the surrounding, during the sampling; residues of cleaning agents, which have been used for

30、 cleaning the sampling equipment and the bottles as well; fuel. A.4 Apparatus A.4.1 Sampling bottles 1000-ml wide neck bottles shall be used. Suited materials for these bottles are HD-polyethylene, HD-polypropylene, polyfluorethylene, polyvinylidenedifluoride and tetrafluoroethylene-perfluoroalky vi

31、nyl ether copolymer (PFA). In case of dispute, PFA bottles should be used. Prior to the first use with AUS 32, the bottles shall be cleaned and finally rinsed with de-ionized water followed by AUS 32. BS ISO 22241-2:20064 A.4.2 Labels Each bottle shall be labelled using labels of approximately 10 cm

32、 5 cm. The labels and the writing on these labels shall be resistant to water and to AUS 32. A.5 Sampling The locked wide-neck bottle shall be opened, the cap shall be put down on a clean surface with the opening turned downward. After flushing the sampling pipe, the bottle shall be filled completel

33、y with AUS 32 from the container. The first filling shall be discarded, and the bottle shall immediately be re-filled with AUS 32 and closed tightly. The label shall be attached to the bottle (see A.4.2). During the filling of the sample, maximum care shall be taken that neither dust nor liquid poll

34、utants get into the bottle. The filled bottle should reach the laboratory as soon as possible. During transportation and storage, the sample should be kept at the lowest possible temperature, preferably between 0 C and 15 C, and kept away from daylight to prevent growth of algae. It is recommended t

35、o conduct the analysis within three weeks in order to take into account possible changes in the ammonia content. A.6 Sample quantity The minimum quantity of sample material depends on the type of analysis conducted. Whenever possible, make sure that a sufficient volume of sample material is availabl

36、e (recommendation: 1 litre), and at least double that which is required for complete verification of AUS 32 specifications. In case of dispute, a sufficient number of samples shall be taken according to ISO 4259. A.7 Labelling The label should contain the following information: product name; name of

37、 the company which owns the sample product 1); address where the sample was taken from 1); manufacturer of the sample product 1); batch or lot number; container from which the sample was taken 1); part of the container where the sample was taken from (sampling point) 1); date and time of sampling 1)

38、; sample shipment date 1); name and signature of the person who took the sample 1). 1) Mandatory only in cases of dispute. BS ISO 22241-2:20065Annex B (normative) Determination of urea content by total nitrogen B.1 General This annex specifies the procedure for determining the urea content of AUS 32

39、. The method is applicable for the determination of the urea content in the range from 30 % to 35 % (m/m). B.2 Principle The sample is combusted at high temperatures in a stream of oxygen. Following the reduction of formed nitrogen oxides to elemental nitrogen and removal of any interfering products

40、 of combustion, nitrogen is measured with a thermal-conductivity detector. The urea content is calculated from the determined total nitrogen minus the nitrogen content of biuret. B.3 Apparatus B.3.1 Automatic nitrogen analyser, based on combustion methods. B.3.2 Analytical balance. The accuracy of t

41、he balance is a function of the analyser used and the required weighed portions. Resolution should be 0,1 % or better of the weighed portion. B.3.3 Auxiliary devices for sample preparation, for example: tweezers with a blunt tip; micro-spatula with a flattened tip; pipette. The pipette is recommende

42、d for weighing in and thus does not need to be calibrated. It is important, however, to obtain a good droplet size (small droplets). Fixed-volume pipettes or pipettes with an adjustable volume in the range from 10 l to 1 000 l or single-trip Pasteur pipettes with a fine tip may also be used. B.3.4 C

43、ustomary chemically resistant glass. B.4 Chemicals B.4.1 De-ionized water, conductivity less than 0,1 mS/m, according to ISO 3696 grade 2. B.4.2 Auxiliary combustion agent and other equipments, appropriate for use with the selected nitrogen analyser. BS ISO 22241-2:20066 The following materials are

44、merely examples. Other or similar materials may be used as required, depending on the system that is available: tin capsule or similar sample containers; auxiliary combustion agent, non-nitrogenous, such as saccharose, cellulose; absorbing agent for liquids, non-nitrogenous, such as magnesium oxide.

45、 B.4.3 Standard substances for nitrogen determination, preferably with certified nitrogen content. EXAMPLE Suitable standard substances include: ethylenediamine tetraacetic acid (EDTA), nicotinic acid amide. Low-biuret urea of adequate purity (for example crystalline ultra pure or analytical) or oth

46、er such standard substances recommended by and available from the equipment manufacturer may also be used. Certified standard substances should be preferred. NOTE Liquid standard substances (e.g. urea solutions) are not suited for calibration purposes. B.4.4 Oxygen, min. 99,995 % O2. B.4.5 Other ult

47、rapure gases, if required to operate the nitrogen analyser, such as helium, min. 99,996 % He. B.4.6 Other reagents or auxiliary agents, as required by the equipment. B.5 Procedure B.5.1 General The sample should be fully dissolved and free from urea crystals. It may be heated to max. 40 C as require

48、d prior to further processing. NOTE Different types of apparatus are available on the market. The resulting various resources and modes of operation are not an object of this part of ISO 22241. Rather, operation should be based on the respective operation manuals. B.5.2 Reference curve Perform calib

49、ration as required for the specific type of analyser and according to the respective operation manuals (for example, after replacement of the combustion tube, reagent or similar) by performing measurements as described in B.5.4. Weigh in an appropriate amount of standard substances repeatedly as appropriate for the respective types of apparatus to obtain a reference curve. B.5.3 Inspecting the apparatus for good working order, and the reference curve Use an appropriate standard substance to review th