ISO-24369-2005.pdf

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1、 Reference number ISO 24369:2005(E) ISO 2005 INTERNATIONAL STANDARD ISO 24369 First edition 2005-10-01 Fine ceramics (advanced ceramics, advanced technical ceramics) Determination of content of coarse particles in ceramic powders by wet sieving method Cramiques techniques Dtermination du contenu en

2、particules grossires des poudres de cramique par la mthode de tamisage humide Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=NASA Technical Standards 1/9972545001 Not for Resale, 04/24/2007 19:34:00 MDTNo reproduction or networking permitted

3、without license from IHS -,-,- ISO 24369:2005(E) PDF disclaimer This PDF file may contain embedded typefaces. In accordance with Adobes licensing policy, this file may be printed or viewed but shall not be edited unless the typefaces which are embedded are licensed to and installed on the computer p

4、erforming the editing. In downloading this file, parties accept therein the responsibility of not infringing Adobes licensing policy. The ISO Central Secretariat accepts no liability in this area. Adobe is a trademark of Adobe Systems Incorporated. Details of the software products used to create thi

5、s PDF file can be found in the General Info relative to the file; the PDF-creation parameters were optimized for printing. Every care has been taken to ensure that the file is suitable for use by ISO member bodies. In the unlikely event that a problem relating to it is found, please inform the Centr

6、al Secretariat at the address given below. ISO 2005 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying and microfilm, without permission in writing from either ISO at

7、 the address below or ISOs member body in the country of the requester. ISO copyright office Case postale 56 CH-1211 Geneva 20 Tel. + 41 22 749 01 11 Fax + 41 22 749 09 47 E-mail copyrightiso.org Web www.iso.org Published in Switzerland ii ISO 2005 All rights reserved Copyright International Organiz

8、ation for Standardization Provided by IHS under license with ISO Licensee=NASA Technical Standards 1/9972545001 Not for Resale, 04/24/2007 19:34:00 MDTNo reproduction or networking permitted without license from IHS -,-,- ISO 24369:2005(E) ISO 2005 All rights reserved iii Contents Page Foreword iv 1

9、 Scope . 1 2 Terms and definitions. 1 3 Apparatus 1 4 Sampling 2 5 Measuring procedures . 2 6 Calculation. 4 7 Report 5 Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=NASA Technical Standards 1/9972545001 Not for Resale, 04/24/2007 19:34:00 M

10、DTNo reproduction or networking permitted without license from IHS -,-,- ISO 24369:2005(E) iv ISO 2005 All rights reserved Foreword ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International

11、 Standards is normally carried out through 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, a

12、lso take part in the work. ISO collaborates 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 commit

13、tees is to prepare International Standards. 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 pos

14、sibility that some of the elements of this document may be the subject of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. ISO 24369 was prepared by Technical Committee ISO/TC 206, Fine ceramics. Copyright International Organization for Standardization

15、Provided by IHS under license with ISO Licensee=NASA Technical Standards 1/9972545001 Not for Resale, 04/24/2007 19:34:00 MDTNo reproduction or networking permitted without license from IHS -,-,- INTERNATIONAL STANDARD ISO 24369:2005(E) ISO 2005 All rights reserved 1 Fine ceramics (advanced ceramics

16、, advanced technical ceramics) Determination of content of coarse particles in ceramic powders by wet sieving method 1 Scope This International Standard specifies the procedure to determine the content of coarse particles in a fine ceramic powder and/or in a fine ceramic suspension using an aqueous-

17、based wet sieving method. The procedure is applicable to fine ceramic powders of both micrometre and submicrometre size ranges. It is valid when there are greater than 10 mg/kg coarse particles in the powders. NOTE It is recommended that new operators of this test method become familiar with the pro

18、cedure, using a reference powder on slurry with a known quantity of coarse particles present. 2 Terms and definitions For the purposes of this document, the following terms and definitions apply. 2.1 coarse particles particles and/or aggregates that cannot pass a 500 mesh sieve with 25 m mesh size 2

19、.2 percentage of coarse particles ratio of the mass of the coarse particles (remaining on the sieve) to the total mass of the powder sample analysed 2.3 suspension ceramic powder suspended in an aqueous medium 2.4 solid content amount of powder in a suspension, ratio of the mass of powder to the tot

20、al mass of the suspension (powder + medium) 3 Apparatus 3.1 Sieve: 500 mesh (the aperture size is 25 m). A stainless-steel rimmed sieve is recommended. 3.2 Analytical balance, having a readability of at least 0,1 mg. 3.3 Bottle: a glass weighing bottle with known mass ma. 3.4 Glass beaker, with a kn

21、own mass me and a volume of at least 250 cm3. Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=NASA Technical Standards 1/9972545001 Not for Resale, 04/24/2007 19:34:00 MDTNo reproduction or networking permitted without license from IHS -,-,- I

22、SO 24369:2005(E) 2 ISO 2005 All rights reserved 3.5 Pipette, 10 ml. 3.6 Oven: capable of controlling a temperature of 105 C 5 C. 3.7 Stirring apparatus: magnetic stirrer and polytetrafluoroethylene (PTFE)-coated stir bar. 3.8 Ultrasonic bath. 3.9 Desiccator or vacuum chamber. 4 Sampling A sample of

23、suspension is required. The amount of powder needed for the measurement is about 30 g 2 g. The solid content of the suspension may vary but must be known (in weight percent). 5 Measuring procedures In the following measuring procedures, humidity is easily adsorbed either from hands or from the air.

24、Therefore, be careful not to touch the sieve and glass weighing bottle with bare hands; use clean tongs or powder-free latex gloves. 5.1 Washing and drying of sieve Submerse the entire sieve in a clean ultrasonic bath filled with distilled water, and ultrasonicate for 10 min. It is recommended that

25、the sieve is upright in the ultrasonic bath to avoid the re-adhesion of undesirable particles. Remove the sieve and drain bath, refill with fresh distilled water, and repeat the treatment. After washing, place the sieve in an oven, and dry it at 105 C for 2 h. After drying, cool the sieve down to ro

26、om temperature in either a desiccator or a vacuum chamber and let it equilibrate there at room temperature for at least 10 min. 5.2 Weighing of sieve After equilibration, determine the mass ms of the sieve, to within 0,1 mg, with a balance directly from the desiccator or vacuum chamber. Calculate th

27、e sieve mass ms* by averaging the values of three measurements, each obtained after equilibration of the balance. 5.3 Determination of solid content The following is the procedure for the determination of solid content. a) Preliminary treatment of the suspension for sampling: mildly agitate the susp

28、ension by shaking or magnetic stirring long enough, so that any sedimentation is compensated for and homogeneity is attained. For a well-dispersed suspension, this might be in the range of 2 to 3 min; for a suspension that is partly deposited, the required time may be up to several hours. Do not use

29、 ultrasonic treatment, as this could influence the coarse particle fraction by rupturing existing agglomerates. b) Take an amount of about 1 to 2 ml of suspension, by means of a pipette, and place it in a glass weighing bottle of known mass ma (to within 0,1 mg). Determine the mass of suspension wit

30、h a glass weighing bottle mb to within 0,1 mg. Calculate the suspension plus bottle mass mb* by averaging the values of three measurements, each obtained after equilibration of the balance. c) Place the weighing bottle with the suspension sample in an oven to dry at 105 C for at least 2 h. After dry

31、ing, transfer the weighing bottle with the dried suspension to either a desiccator or a vacuum chamber for cooling to room temperature, and let it equilibrate there at room temperature for at least 10 min. Copyright International Organization for Standardization Provided by IHS under license with IS

32、O Licensee=NASA Technical Standards 1/9972545001 Not for Resale, 04/24/2007 19:34:00 MDTNo reproduction or networking permitted without license from IHS -,-,- ISO 24369:2005(E) ISO 2005 All rights reserved 3 d) After equilibrating, determine the mass of the glass weighing bottle with the dried suspe

33、nsion mc, to within 0,1 mg, directly from the desiccator or vacuum chamber. Calculate the sample plus bottle mass mc* by averaging the values of three measurements, each obtained after equilibration of the balance. e) Calculation of the solid content SC as a ratio of masses of powder and suspension:

34、 msuspension = mb* ma, in grams (1) mpowder = mc* ma, in grams (2) powder suspension SC m m = (3) 5.4 Sampling and determination of mass of suspended powder The following is the procedure for sampling and determination of mass of suspended powder. a) Preliminary treatment of the suspension for sampl

35、ing: mildly agitate the suspension by shaking or magnetic stirring, for long enough so that any sedimentation is compensated for and homogeneity is attained. For a well-dispersed suspension, this might be in the range of 2 3 min; for a suspension that is partly deposited, the required time may be up

36、 to several hours. Do not use ultrasonic treatment, as this could influence the coarse particle fraction by rupturing existing agglomerates. b) The absolute amount of powder needed is about 30 g. Therefore, the sample for measurement is obtained from the suspension with a now known SC by weighing. T

37、he amount used depends on the solid content, so that the amount of powder is about 30 g 2 g. The required mass of suspension can be calculated by msuspension = powder SC m (4) EXAMPLE When SC in a suspension is 0.3, 100 g of a suspension is required. Also, 37,5 g of a suspension is required when SC

38、is 0,8. c) Place the required amount of suspension into a beaker of known mass me (to within 0,1 mg). Determine the mass mf of beaker with suspension to within 0,1 mg. Determine the suspension plus beaker mass mf* by averaging the values of three measurements, each obtained after equilibration of th

39、e balance. The mass mg of the suspension is given by Equation (5) mg = mf* me (5) According to Equation (4), the mass mp of the powder in the suspension is given by mp = mg SC (6) 5.5 Separation of coarse particles The following is the procedure for separation of coarse particles. a) Wet the sieve a

40、nd place it in the shallow washing bath. Adjust the level of the mesh so that it is just below the water surface of the bath. In this way, the mesh of the sieve will be covered with water. Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=NASA T

41、echnical Standards 1/9972545001 Not for Resale, 04/24/2007 19:34:00 MDTNo reproduction or networking permitted without license from IHS -,-,- ISO 24369:2005(E) 4 ISO 2005 All rights reserved b) Pour the sample suspension slowly, and little by little, into the sieve so that nothing of the suspension

42、is lost. In case the sieve becomes clogged with material, dilute and disperse the clogged material by pouring distilled water into the sieve. Take care that the suspension is quantitatively transferred to the sieve by rinsing the beaker with distilled water at the end. NOTE 1 Coarse particles tend t

43、o sediment during slow pouring, and therefore concentrate in the last 5 10 % of the slurry. Coarse particles may adhere to a glass beaker. It is recommended to dry the beaker and inspect retained coarse particles. If these are found, they should be removed with water and the resultant suspension sho

44、uld be wet-sieved. c) Rinse away any suspension that is attached to the sieve frame with distilled water, then pour a sufficient amount or volume of distilled water into the sieve. NOTE 2 About 10 L might be a sufficient volume. d) Take care that all particles are on the mesh of the sieve and nothin

45、g is left on the sieve frame. e) If the slurry viscosity is excessively high, dilute the slurry with a proper liquid, for which the chemistry is the same as that of the supernatant of the slurry. Alternatively, take care that the mesh of the sieve be covered with water, with no air bubbles between t

46、he mesh and water surface, during sieving. 5.6 Drying and weighing of sieve with coarse particles Follow the same procedures as detailed in 5.1 and 5.2 to measure the mass mscp* of the sieve with coarse particles. 5.7 Washing the sieve Wash the sieve upside down for 10 min in clean water in an ultra

47、sonic bath. Remove the sieve and turn it over, so that the mesh is upright, and wash for an additional 10 min. Drain the bath and refill with fresh water. Repeat the washing treatment. Dry the sieve as in 5.1. 6 Calculation The percentage X of coarse particles in the powder, in milligrams per kilogr

48、am, can now be determined according to Equation (7). scp*s* 6 p 10 mm X m = (7) where mscp* is the mass, in grams, of sieve plus coarse particle (5.5); ms* is the sieve mass, in grams, before the experiments (5.1); mp is the determined mass, in grams, of powder. The values of mscp* and ms* are the average ones. Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=NASA Technical Standards 1/9972545001 Not for Resale, 04/24/2007 19:34:00 MDTNo reproduction or networking permitted without license

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