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Studies in dyeing and cleaning ...Lake, Dyer Barker, January 1900 (has links)
Thesis (Ph. D.)--Cornell University, 1916. / "Reprinted from the Journal of physical chemistry, 20, 761 (1916)."
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Methyl isopropyl indigoid dyes from cymene ...Cauwenberg, Winfred Joseph, January 1930 (has links)
Thesis (Ph. D.)--Columbia University, 1930. / Vita. "Literature cited": p. [44].
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The applicability of selected methods of dye identification to natural and synthetic fibersGilligan, Helen T. January 1959 (has links)
Thesis (M.S.)--University of Wisconsin--Madison, 1959. / Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 39-40).
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T bouck vā wondre, 1513 ...Frencken, Herman Gerard Theodoor, January 1934 (has links)
Proefschrift--Leiden. / The work was originally published in Brussels in 1513.
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The effect of sulfur on the color of triphenyl methane dyes and certain phthaleinsHolt, Harold Stephens. January 1924 (has links)
Thesis (Ph. D.)--Johns Hopkins University, 1924. / Description based on print version record. Includes bibliographical references.
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Constitution and color in the thioflavine groupTaylor, William S. January 1931 (has links)
Thesis--Columbia University, 1932. / Vita. Bibliography: p. [35].
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The Stieglitz theory of color production ...Cole, Robert MacFarlan, January 1940 (has links)
Thesis (Ph. D.)--University of Chicago, 1937. / Lithoprinted. "Private edition, distributed by the University of Chicago libraries, Chicago, Illinois."
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Columbia yellow, its structure and related intermediates ...Bergeim, Frank Herbert, January 1924 (has links)
Thesis (Ph. D.)--Columbia University, 1924. / Biographical. Bibliography: p. 26.
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The introduction of colored radicals into organic molecules.Gentry, Willard Max January 1951 (has links)
Thesis (Ph.D.)--Boston University / The principal purpose of this investigation was to devise a means whereby natural or synthetic fibers might be dyed by the formation of ether, ester, or amide linkages. By so doing, the dyeing process would result in a very fast coloration unaffected by washing.
For the purposes of preparing a colored ether of natural fibers, reactions wit h cellulose were tried with p-bromonitrosobenzene . It was hoped that this would give a p-nitrosophenyl ether of cellulose. This compound might itself be colored; but more important, it could be coupled with a variety of amines to give azo compounds. The compound p- br omonitrosobenzene, was chosen as the reagent for accomplishing this etherification, because it was the simplest, readily available nitrosocompound with a halogen group that could react fairly easily with cellulose.
Attempts to prepare such a cellulose ether failed. The use of soda cellulose, or cellulose dissolved in benzyltrimethylammonium hydroxide, in a manner analogous to normal cellulose etherification reactions, resulted in failures. Rather than reacting with the cellulose, the nitroso compound decomposed rapidly to give p,p 1-dlbromoazoxybenzene in high yield. [TRUNCATED]
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The mode of action of vital dyesGregory, Jennifer M. January 1964 (has links)
No description available.
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