PIA-TEST METHOD-2611D-2014 NONFIBROUS MATERIALS IN COTTON ENZYME METHOD.pdf
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1、 The following commercial specification is adopted from the military document. Revision A includes all known accepted revisions, amendments, notices, and Department of Defense (DoD) engineering changes previously developed for this item. Revisions B and forward include changes adopted to reflect tec
2、hnology and design evolution. NONFIBROUS MATERIALS IN COTTON, ENZYME METHOD The Parachute Industry Association makes this document available for use by Industry and Government organizations that wish to apply this specification to their products. 1. SCOPE 1.1 This method is intended for determining,
3、 in cotton or cellulosic mixture yarns or cloths, the amount of sizing, finishing, and other nonfibrous materials, such as oils, fats, waxes, minerals, and other materials which will be removed or determined by chloroform and/or water extraction, hydrolized by enzyme action, or remain as inorganic m
4、aterial after exposure to high temperatures. Although this method is intended for the determination of nonfibrous materials in cellulosic textiles, it may be used for determining the extractable and nonfibrous materials content of certain noncellulosic textiles, as specified in the applicable end it
5、em specification or procurement document. 1.2 This method is not applicable to the determination of the amount of permanent types of finishes, such as urea condensates, melamine condensates, and substantive or organic finished, or to finishes that are volatile at 230F (110C). 2. TEST SPECIMEN 2.1 Th
6、e specimen shall be approximately 10 g of the material undergoing test. Care should be taken in the preparation and subsequent handling of the specimen, so that loss of material will not occur during test. If the material undergoing test is woven or knitted cloth, the specimen should be cut on the b
7、ias and have loose fibers and yarns removed. 2.1.1 When total ash is required, an additional 10 g specimen is required for evaluation. 3. NUMBER OF DETERMINATIONS 3.1 Unless otherwise specified in the procurement document, two specimens shall be tested from each sample unit. 4. APPARATUS AND REAGENT
8、S DISTRIBUTION STATEMENT: All Rights Reserved. No Part of this publication may be reproduced without prior written permission from Parachute Industry Association. Additional copies may be purchased on-line from PIA Specifications and Products: . PIA-TEST METHOD-2611D 04 June 2014 Superseding PIA-TES
9、T METHOD-2611C 24 May 2010 Copyright Protected: Do Not Copy!PIA-TEST METHOD-2611D 4.1 Apparatus. 4.1.1 Analytical balance. Analytical balance capable of weighing accurately to 0.001 g. 4.1.2 Weighing bottle with ground glass cover. 4.1.3 Soxhlet extraction apparatus. 4.1.4 Muffle furnace. 4.1.5 Stai
10、nless steel sieve. 80 to 100 mesh or equivalent. 4.1.6 Desiccator with suitable desiccant. Anhydrous calcium sulfate or anhydrous calcium chloride have been found suitable. 4.2 Reagents. 4.2.1 Chloroform, U.S.P. 4.2.2 Iodine solution. An approximate 0.01N stock solution of iodine (0.13 g of iodine a
11、nd 2.6 g of KI in 100 ml of water) may be prepared, and a portion of this diluted to a pale yellow color (about 0.001N) each time a test for starch is made. 4.2.3 Amylolytic and proteolytic enzyme mixture (see 7.1). 4.2.4 Millons reagent. Millons reagent shall be prepared by adding 25 g (17.6 ml) co
12、ncentrated nitric acid (sp. gr. 1.42) to 25 g (1.84 ml) of mercury under a hood. Upon completion of the reaction, the solution shall be diluted by adding in equal volumes of distilled water. 5. PROCEDURE 5.1 Weight of dry specimen. The specimen shall be placed in a weighing bottle and dried in an ov
13、en at a temperature of 221 to 230 F (105 to 110C), cooled in a desiccator, and weighed to the nearest 0.001 g. This is the “Weight of the dry specimen” and in the calculation of results is indicated as “0”. 5.2 Chloroform-soluble material. The dried specimen from 5.1 shall be extracted with chlorofo
14、rm for a minimum of 20 extractions in Soxhlet extractor. If the weight of the chloroform-extractable matter is required, the extract shall be dried to constant weight in a tared container at a temperature of 174 to 178F (79 to 81C), cooled in a desiccator, and weighed to the nearest 0.001 g. This is
15、 the “Weight of chloroform-soluble material” and in the calculation of results is indicated as “C”. 5.3 Water-soluble material. The specimen from 5.2 shall be placed in a Soxhlet extractor with distilled water and subjected to a minimum of 10 extractions. If the weight of the material is required, t
16、he extract shall be dried to constant weight in a tared container at a temperature of 212 to 215F (100 to 102C), cooled in a desiccator, and weighed to the nearest 0.001 g. This is the “Weight of the water soluble material”, and in the calculation of results is indicated as “W”. Page 2 of 5 Copyrigh
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