Textile chemistry

R. H. Peters, Textile Chemistry Wolume III, Elsevier Pubhshers, New York, 1975. 

Chemical compounds that contain methylol groups (-CH2 OH) form stable, covalent bonds with cellulose fibers. Those compounds are well known and widely used in textile chemistry. Hydrogen bonds with cellulose can be formed in this reaction as well. The treatment of cellulose with methylolmelamine compounds before forming cellulose unsaturated polyesters (UP) composites decreases the moisture pickup and increases the wet strength of reinforced plastic [48,49]. 

Working first with Polanyi, Weissenberg, and Brill, and later as the leader of the Textile Chemistry Section, Mark successively published papers on the crystal structures of hexamethylenetetramine, pentaerythritol, zinc salts, tin, urea, tin salts, triphenylmethane, bismuth, graphite, sulfur, oxalic acid, acetaldehyde, ammonia, ethane, diborane, carbon dioxide, and some aluminum silicates. Each paper showed his and the laboratory s increasing sophistication in the technique of X-ray diffraction. Their work over the period broadened to include contributions to the theories of atomic and molecular structure and X-ray scattering theory. A number of his papers were particularly notable including his work with Polanyi on the structure of white tin ( 3, 4 ), E. Wigner on the structure of rhombic sulfur (5), and E. Pohland on the low temperature crystal structure of ammonia and carbon dioxide (6, 7). The Mark-Szilard effect, a classical component of X-ray physics, was a result of his collaboration with Leo Szilard (8). And his work with E. A. Hauser (9, 10, 11) on rubber and J. R. 

North Carolina State University, School of Textiles, Department of Textile Chemistry, Raleigh, NC 27650... 

Developed from a symposium sponsored by the ACS Divisions of Carbohydrate Chemistry Cellulose, Paper, and Textile Chemistry and Computers in Chemistry at the 197th National Meeting Dallas, Texas,... 

Bechtold, T. Burtscher, E. Bobleter, O. Application of electrochemical processes and electro-analytical methods in textile chemistry. Curr. Topics Electrochem. 1998, 6, 97-110. 

Peters, R. H. The Physical Chemistry of Dyeing, Textile Chemistry, Vol. 3, New York Elsevier 1975... 

Illingworth, J. W. Post-advanced course in textile chemistry, Manchester College of Technology, 1942—43 cf. G. Landells and C. S. Whewell J. Soc. Dyers Colorists 67, 338 (1951). 

Based on a symposium jointly sponsored by the Divisions of Industrial and Engineering Chemistry, Colloid and Surface Chemistry, Petroleum Chemistry, and Paper and Textile Chemistry at the 182nd Meeting of the American Chemical Society, New York, New York, August 23-28, 1981. ... 

Hartsuch, B. E. Introduction to Textile Chemistry. Wiley New York. 1950. 139. 

Alfred D. French and John W. Brady, Computer Modeling of Carbohydrate Molecules. Developed from a symposium by the ACS Divisions of Carbohydrate Chemistry, Cellulose, Paper, and Textile Chemistry and Computers in Chemistry, at the 197th National Meeting, Dallas, Texas, April 9-14, 1989, in ACS Symposium Series 430, American Chemical Society, Washington, DC, 1990. 

Dresden Polymer Discussions have been organized by the Leibniz Institute of Polymer Research Dresden and the Institute of Macromolecular and Textile Chemistry of the Technische Universitat Dresden now since 1986. Every two years, interested scientists, researchers and students from polymer research centres, universities and industry from all over the world discuss latest results, trends and new demands on research and development in different fields of polymer science. 

Bell, J. W., Practical Textile Chemistry, p. 27, Chemical Publishing, New... 

Traore, M. K., and Buschle-Diller, G. 1999. Influence of wetting agents and agitation on enzymatic hydrolysis of cotton. Textile Chemistry Colorist American Dyestuff... 

Peters, R. H., Textile Chemistry The Chemistry of Fibers, Vol. I and Impurities in Fibers Purification of Fibers, Vol. II, Elsevier, New York, 1963 and 1967. 

Matthews, J. M. Laboratory Manual of Dyeing and Textile Chemistry, ... 

Microwave heating techniques have been widely used in textile chemistry. This paper presents a state-of-the-art review of microwave technologies and industrial applications. The characteristics of microwave interactions with textile materials are outlined together with microwave fundamentals in the heat-setting process. Further more, the limitations in current imderstanding are included as a guide for potential users and for future research and development activities. 

Thibodeaux, D.P. and Copeland, H.R., Corona treating cotton its relationship to processing performance and quality. Proceedings of the 15th Textile Chemistry and Processing Conference, New Orleans, 1975, 36. 

Pseudo-stilbenes may emit fluorescence that is, contrary to true stilbenes, generally weak at room temperature and often weak even at low temperatures. Protonated azobenzene-type molecules and many protonated azo dye molecules emit strong fluorescence in sulfuric acid at 77 K with quantum yields of about 0.1. Inclusion of azobenzene in the channels of AIPO4-5 crystals provides complexation of the n-electrons and space confinement. This leads to emission by protonated azobenzene at room temperature. For their cyclopalladated azobenzenes, Ghedini et al. " report quantum yields of ca. 1T0 and lifetimes of ca. 1 ns. In contrast, donor/acceptor pseudo-stilbenes, if emitting at low temperatures or when adsorbed to surfaces, are weak emitters. In textile chemistry, it has long been known that azo dyes adsorbed to fibers may show fluorescence. ... 

Institute for Textile Chemistry and Textile Physics, Dornbirn, Austria (vat dyes recycling)... 

Professor of Textile Chemistry College of Textile Technology Serampore, Hooghly, West Bengal India... 

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