1977
DOI: 10.1021/i360061a021
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Nylon-1313 from Brassylic Acid

Abstract: The mention of firm names or trade products does not imply that they are endorsed or recommended by the Department of Agriculture over other firms or similar products not mentioned.

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Cited by 35 publications
(24 citation statements)
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References 9 publications
(12 reference statements)
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“…Besides, T g and mechanical properties of the copolyamides were higher than that of PA11 and PA12. In addition, compared to PA12, 14, PA10, 10, PA 10, 12, PA13, 13, PA10, 13, PA12, 13, and PA 10, 13, the PA6‐BABA/SA copolyamides have similar thermal properties and high mechanical properties, which indicate that the as synthesized PA6‐BABA/SA have excellent thermal and mechanical properties.…”
Section: Resultsmentioning
confidence: 97%
“…Besides, T g and mechanical properties of the copolyamides were higher than that of PA11 and PA12. In addition, compared to PA12, 14, PA10, 10, PA 10, 12, PA13, 13, PA10, 13, PA12, 13, and PA 10, 13, the PA6‐BABA/SA copolyamides have similar thermal properties and high mechanical properties, which indicate that the as synthesized PA6‐BABA/SA have excellent thermal and mechanical properties.…”
Section: Resultsmentioning
confidence: 97%
“…Similarly, PA 11 is being promoted from the same natural source. Nieschlag et al [40] prepared PA 1313 based entirely on components derived from erucic acid oils, derived from various seed plants. Evonik Industries [41] manufacture PA 610 polymer (Vestamide 1 Terra HS) of partially natural source and also a PA 1010 polymer (Vestamid 1 Terra DS) with both monomers derived from castor oil.…”
Section: Polyamides From Straight-chain Aliphatic Monomersmentioning
confidence: 99%
“…9‐hydroxynonanoic acid, prepared from oleic acid, can be considered as a potential starting precursor for aliphatic polynonanolactone via a 10‐membered nonanolactone cyclic monomer. The synthetic route for producing nonanolactone from oleic acid is similar to that used in the preparation of various Nylon monomers from renewable resources 22–24. Previous studies show that dilactone (1,11‐dioxacycloicosane‐2,12‐dione) was exclusively formed with a very low yield of monolactone;25, 26 however, there are a few reports which explains the synthesis of monolactone with comparatively high yield 27.…”
Section: Introductionmentioning
confidence: 99%