Surface Modification of Poly(<span style="font-variant: small-caps">l</span>-lactic acid) through Stereocomplexation with Enantiomeric Poly(<span style="font-variant: small-caps">d</span>-lactic acid) and Its Copolymer

Poly(<span style="font-variant: small-caps;">l</span>-lactic acid) with high molecular weight was used to prepare PLLA films by means of the solvent casting technique. Poly(<span style="font-variant: small-caps;">d</span>-lactic acid) (PDLA) and poly(<s...

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Main Authors: Qianjin Zhu, Kaixin Chang, Liyan Qi, Xinyi Li, Woming Gao, Qinwei Gao
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Polymers
Subjects:
Online Access:https://www.mdpi.com/2073-4360/13/11/1757
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spelling doaj-24571282fe6e4634a9e2d34c24bd8ba62021-06-01T01:20:14ZengMDPI AGPolymers2073-43602021-05-01131757175710.3390/polym13111757Surface Modification of Poly(<span style="font-variant: small-caps">l</span>-lactic acid) through Stereocomplexation with Enantiomeric Poly(<span style="font-variant: small-caps">d</span>-lactic acid) and Its CopolymerQianjin Zhu0Kaixin Chang1Liyan Qi2Xinyi Li3Woming Gao4Qinwei Gao5College of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, ChinaCollege of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, ChinaCollege of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, ChinaCollege of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, ChinaCollege of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, ChinaCollege of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, ChinaPoly(<span style="font-variant: small-caps;">l</span>-lactic acid) with high molecular weight was used to prepare PLLA films by means of the solvent casting technique. Poly(<span style="font-variant: small-caps;">d</span>-lactic acid) (PDLA) and poly(<span style="font-variant: small-caps;">d</span>-lactic acid-<i>co</i>-glucose) copolymer (PDLAG) with a low molecular weight were synthesized from <span style="font-variant: small-caps;">d</span>-lactic acid and glucose through melt polycondensation. PLLA films were immersed in PDLA or PDLAG solution to prepare surface-modified PLLA films. The modified PLLA film presented stereocomplex crystal (SC) on its surface and homogeneous crystals (HC) in its bulk. The HC structure and surface morphology of modified PLLA films were obviously damaged by PDLA or PDLAG solution. With increasing immersion time, the PLLA films modified by PDLA decreased both the HC and SC structure, while the PLLA films modified by PDLAG increased the SC structure and decreased the HC structure. Hydrophilic glucose residues of PDLAG on the surface would improve the hydrophilicity of surface-modified PLLA films. Moreover, the hydrophilicity of glucose residues and the interaction of glucose residues with lactic acid units could retard HC destruction and SC crystallization, so that PLLA films modified by PDLAG possessed lower melting temperatures of HC and SC, the crystallinity of SC and the water contact angle, compared with PDLAG-modified PLLA films. The SC structure could improve the heat resistance of modified PLLA film, but glucose residues could block crystallization to promote the thermal degradation of PLA materials. The surface modification of PLLA films will improve the thermal stability, hydrophilicity and crystallization properties of PLA materials, which is essential in order to obtain PLA-based biomaterials.https://www.mdpi.com/2073-4360/13/11/1757poly(<span style="font-variant: small-caps">l</span>-lactic acid)poly(<span style="font-variant: small-caps">d</span>-lactic acid)poly(<span style="font-variant: small-caps">d</span>-lactic acid-<i>co</i>-glucose)stereocomplexsurface modification
collection DOAJ
language English
format Article
sources DOAJ
author Qianjin Zhu
Kaixin Chang
Liyan Qi
Xinyi Li
Woming Gao
Qinwei Gao
spellingShingle Qianjin Zhu
Kaixin Chang
Liyan Qi
Xinyi Li
Woming Gao
Qinwei Gao
Surface Modification of Poly(<span style="font-variant: small-caps">l</span>-lactic acid) through Stereocomplexation with Enantiomeric Poly(<span style="font-variant: small-caps">d</span>-lactic acid) and Its Copolymer
Polymers
poly(<span style="font-variant: small-caps">l</span>-lactic acid)
poly(<span style="font-variant: small-caps">d</span>-lactic acid)
poly(<span style="font-variant: small-caps">d</span>-lactic acid-<i>co</i>-glucose)
stereocomplex
surface modification
author_facet Qianjin Zhu
Kaixin Chang
Liyan Qi
Xinyi Li
Woming Gao
Qinwei Gao
author_sort Qianjin Zhu
title Surface Modification of Poly(<span style="font-variant: small-caps">l</span>-lactic acid) through Stereocomplexation with Enantiomeric Poly(<span style="font-variant: small-caps">d</span>-lactic acid) and Its Copolymer
title_short Surface Modification of Poly(<span style="font-variant: small-caps">l</span>-lactic acid) through Stereocomplexation with Enantiomeric Poly(<span style="font-variant: small-caps">d</span>-lactic acid) and Its Copolymer
title_full Surface Modification of Poly(<span style="font-variant: small-caps">l</span>-lactic acid) through Stereocomplexation with Enantiomeric Poly(<span style="font-variant: small-caps">d</span>-lactic acid) and Its Copolymer
title_fullStr Surface Modification of Poly(<span style="font-variant: small-caps">l</span>-lactic acid) through Stereocomplexation with Enantiomeric Poly(<span style="font-variant: small-caps">d</span>-lactic acid) and Its Copolymer
title_full_unstemmed Surface Modification of Poly(<span style="font-variant: small-caps">l</span>-lactic acid) through Stereocomplexation with Enantiomeric Poly(<span style="font-variant: small-caps">d</span>-lactic acid) and Its Copolymer
title_sort surface modification of poly(<span style="font-variant: small-caps">l</span>-lactic acid) through stereocomplexation with enantiomeric poly(<span style="font-variant: small-caps">d</span>-lactic acid) and its copolymer
publisher MDPI AG
series Polymers
issn 2073-4360
publishDate 2021-05-01
description Poly(<span style="font-variant: small-caps;">l</span>-lactic acid) with high molecular weight was used to prepare PLLA films by means of the solvent casting technique. Poly(<span style="font-variant: small-caps;">d</span>-lactic acid) (PDLA) and poly(<span style="font-variant: small-caps;">d</span>-lactic acid-<i>co</i>-glucose) copolymer (PDLAG) with a low molecular weight were synthesized from <span style="font-variant: small-caps;">d</span>-lactic acid and glucose through melt polycondensation. PLLA films were immersed in PDLA or PDLAG solution to prepare surface-modified PLLA films. The modified PLLA film presented stereocomplex crystal (SC) on its surface and homogeneous crystals (HC) in its bulk. The HC structure and surface morphology of modified PLLA films were obviously damaged by PDLA or PDLAG solution. With increasing immersion time, the PLLA films modified by PDLA decreased both the HC and SC structure, while the PLLA films modified by PDLAG increased the SC structure and decreased the HC structure. Hydrophilic glucose residues of PDLAG on the surface would improve the hydrophilicity of surface-modified PLLA films. Moreover, the hydrophilicity of glucose residues and the interaction of glucose residues with lactic acid units could retard HC destruction and SC crystallization, so that PLLA films modified by PDLAG possessed lower melting temperatures of HC and SC, the crystallinity of SC and the water contact angle, compared with PDLAG-modified PLLA films. The SC structure could improve the heat resistance of modified PLLA film, but glucose residues could block crystallization to promote the thermal degradation of PLA materials. The surface modification of PLLA films will improve the thermal stability, hydrophilicity and crystallization properties of PLA materials, which is essential in order to obtain PLA-based biomaterials.
topic poly(<span style="font-variant: small-caps">l</span>-lactic acid)
poly(<span style="font-variant: small-caps">d</span>-lactic acid)
poly(<span style="font-variant: small-caps">d</span>-lactic acid-<i>co</i>-glucose)
stereocomplex
surface modification
url https://www.mdpi.com/2073-4360/13/11/1757
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