1953
DOI: 10.1007/bf02165821
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Darstellung von Polyasparaginsäuren (Polyaspartsäuren) aus dem thermischen Autokondensationsprodukt der Asparaginsäure

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Cited by 48 publications
(11 citation statements)
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“…(Kovacs et al, 1953;Kovacs et a1., 1961). They prepared polyaspartic acid anhydride by heating DL-aspartic acid at about 180-Z00°C.…”
Section: Polyglycinementioning
confidence: 99%
“…(Kovacs et al, 1953;Kovacs et a1., 1961). They prepared polyaspartic acid anhydride by heating DL-aspartic acid at about 180-Z00°C.…”
Section: Polyglycinementioning
confidence: 99%
“…A number of polyacrylates such as poly(sodium acrylate) [2], sodium salt of maleic anhydride-isobutylene copolymer and maleic anhydride-vinyl acetate copolymer have been reported to give excellent builder performances in detergent formulations as compared with sodium tripolyphosphate (STPP). However, they are hardly biodegradable except for their oligomers [3][4][5], which will possibly produce much damage to the environment. Therefore, the biodegradable substitutes for non-biodegradable polymers having carboxylic acid groups are really desirable with a view to protecting the environment.…”
Section: Introductionmentioning
confidence: 99%
“…Excessive heating of amino acids usually results in the formation of carbonized tar. However, aspartic acid (Kovacs et al 1953 ;Vegotsky et al 1958), glutamic acids , lysine (Harada 1959a) and their ammonium salts and amides (Harada 1959b) were found to undergo selfcondensation and copolymerization with other amino acids by simple heating, because heating of aspartic acid or glutamic acids as well as lysine produces polymerizable intermediates, such as intramolecular anhydrides, imides or amides. The lactams of glutamic acid or lysine in the molten state also served as polar reaction media, facilitating thermal polycondensation.…”
Section: Introductionmentioning
confidence: 99%