Nucleating agent for poly(L-lactic acid)-An optimization of chemical structure of hydrazide compound for advanced nucleation ability

A series of compounds having hydrazide groups was prepared and evaluated as nucleating agent for poly(L‐lactic acid) by differential scanning calorimetry. Hydrazide compounds derived from benzoic acid, 2‐hydroxybenzoic acid, 3‐tert‐butylbenzoic acid, and 2‐aminobenzoic acid, where two of hydrazide c...

Full description

Saved in:
Bibliographic Details
Published inJournal of applied polymer science Vol. 103; no. 1; pp. 198 - 203
Main Authors Kawamoto, N., Sakai, A., Horikoshi, T., Urushihara, T., Tobita, E.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 05.01.2007
Wiley
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:A series of compounds having hydrazide groups was prepared and evaluated as nucleating agent for poly(L‐lactic acid) by differential scanning calorimetry. Hydrazide compounds derived from benzoic acid, 2‐hydroxybenzoic acid, 3‐tert‐butylbenzoic acid, and 2‐aminobenzoic acid, where two of hydrazide compounds connected by four methylene chain were evaluated in series. Benzoylhydrazide type was found to be more effective on the enhancement of crystallization of poly(L‐lactic acid). Effects of connecting length of methylene chain numbers between two of benzoylhydrazide on the nucleation ability were also evaluated. Benzoylhydrazide‐type compound having 10 methylenes, that is, decamethylenedicarboxylic dibenzoylhydrazide demonstrated excellent nucleation ability, and the resulted crystallization temperature and enthalpy of PLA with the compound of 1 wt % loading were 131°C and 46 J g−1. The achieved crystallization temperature and enthalpy were over 10°C and over 10 J g−1 higher than PLA with conventional nucleating agents, such as talc and ethylenebis (12‐hydroxystearylamide). Thus, the improvement in processability, productivity, and heat resistance of PLA is suggested to be achieved by using decamethylenedicarboxylic dibenzoylhydrazide as a nucleating agent. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 198–203, 2007
Bibliography:ArticleID:APP25109
istex:15DD82A6176EAF138274FEF126DB963A79DC7815
ark:/67375/WNG-5Z78CQCR-8
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0021-8995
1097-4628
DOI:10.1002/app.25109