Miscibility and hydrolytic degradation in alkaline solution of poly( l-lactide) and poly( p-vinyl phenol) blends
Poly( l-lactide) (PLLA) was melt-blended with poly( p-vinyl phenol) (PVPh) using a two-roll mill, and the miscibility between PLLA and PVPh and degradation of the blend films were investigated. It was found that PLLA/PVPh blend has miscibility in the amorphous state because only single T g was obser...
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| Published in | Polymer Degradation and Stability Vol. 92; no. 8; pp. 1626 - 1631 |
|---|---|
| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Oxford
Elsevier Ltd
01.08.2007
Elsevier BV Elsevier Science |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0141-3910 1873-2321 |
| DOI | 10.1016/j.polymdegradstab.2007.04.003 |
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| Abstract | Poly(
l-lactide) (PLLA) was melt-blended with poly(
p-vinyl phenol) (PVPh) using a two-roll mill, and the miscibility between PLLA and PVPh and degradation of the blend films were investigated. It was found that PLLA/PVPh blend has miscibility in the amorphous state because only single
T
g was observed in the DSC and DMA measurements. The
T
g of the PLLA/PVPh blend could be controlled in the temperature range from 55
°C to 117
°C by changing the PVPh weight fraction. In alkaline solution, degradation rate of PLLA/PVPh blends was faster than that of neat PLLA because PVPh could dissolve in alkaline solution. The surface morphology of degraded PLLA and PLLA/PVPh blend were observed by SEM. The surface morphology of degraded PLLA/PVPh blend was finer than that of PLLA. Young's modulus of PLLA/PVPh blend increased with increasing PVPh content. Yield stress of PLLA/PVPh blends whose PVPh content was less than 30
wt% kept the level of about 55
MPa and that of PLLA/PVPh blend whose PVPh content was 40
wt% is much lower than that of neat PLLA. |
|---|---|
| AbstractList | Poly(
l-lactide) (PLLA) was melt-blended with poly(
p-vinyl phenol) (PVPh) using a two-roll mill, and the miscibility between PLLA and PVPh and degradation of the blend films were investigated. It was found that PLLA/PVPh blend has miscibility in the amorphous state because only single
T
g was observed in the DSC and DMA measurements. The
T
g of the PLLA/PVPh blend could be controlled in the temperature range from 55
°C to 117
°C by changing the PVPh weight fraction. In alkaline solution, degradation rate of PLLA/PVPh blends was faster than that of neat PLLA because PVPh could dissolve in alkaline solution. The surface morphology of degraded PLLA and PLLA/PVPh blend were observed by SEM. The surface morphology of degraded PLLA/PVPh blend was finer than that of PLLA. Young's modulus of PLLA/PVPh blend increased with increasing PVPh content. Yield stress of PLLA/PVPh blends whose PVPh content was less than 30
wt% kept the level of about 55
MPa and that of PLLA/PVPh blend whose PVPh content was 40
wt% is much lower than that of neat PLLA. Poly(l-lactide) (PLLA) was melt-blended with poly(p-vinyl phenol) (PVPh) using a two-roll mill, and the miscibility between PLLA and PVPh and degradation of the blend films were investigated. It was found that PLLA/PVPh blend has miscibility in the amorphous state because only single Tg was observed in the DSC and DMA measurements. The Tg of the PLLA/PVPh blend could be controlled in the temperature range from 55 deg C to 117 deg C by changing the PVPh weight fraction. In alkaline solution, degradation rate of PLLA/PVPh blends was faster than that of neat PLLA because PVPh could dissolve in alkaline solution. The surface morphology of degraded PLLA and PLLA/PVPh blend were observed by SEM. The surface morphology of degraded PLLA/PVPh blend was finer than that of PLLA. Young's modulus of PLLA/PVPh blend increased with increasing PVPh content. Yield stress of PLLA/PVPh blends whose PVPh content was less than 30wt% kept the level of about 55MPa and that of PLLA/PVPh blend whose PVPh content was 40wt% is much lower than that of neat PLLA. |
| Author | Sumita, Masao Tominaga, Yoichi Komatsu, Yoichi Shirahase, Tomoko Marubayashi, Hironori Asai, Shigeo |
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| Cites_doi | 10.1002/(SICI)1097-4628(19980118)67:3<405::AID-APP3>3.0.CO;2-Q 10.1016/S0032-3861(97)10167-7 10.1021/ma047818f 10.1016/S0141-3910(00)00192-0 10.1016/S0141-8130(01)00158-1 10.1002/polb.10353 10.1016/S0032-3861(96)00455-7 10.1016/S0014-3057(99)00068-3 10.1002/(SICI)1097-4636(199602)30:2<201::AID-JBM10>3.0.CO;2-P 10.1016/j.biomaterials.2003.08.060 10.1016/S0142-9612(02)00365-4 10.1016/S0032-3861(98)00182-7 10.1016/S0032-3861(98)00463-7 10.1016/0032-3861(95)90987-D 10.1016/0032-3861(96)82913-2 10.1016/j.polymer.2006.04.012 |
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| Keywords | Degradation Poly( l-lactide) Heat resistance improvement Polymer blend Miscible blend Elastic modulus Polymer blends Property composition relationship Mechanical properties Chemical degradation Poly(L-lactide) Experimental study Lactone polymer Styrene(hydroxy) polymer Hydrolysis Hydrolysis resistance Lactic acid polymer Morphology Aliphatic polymer Miscibility Basic medium Chemical properties Thermodynamic properties |
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| Snippet | Poly(
l-lactide) (PLLA) was melt-blended with poly(
p-vinyl phenol) (PVPh) using a two-roll mill, and the miscibility between PLLA and PVPh and degradation of... Poly(l-lactide) (PLLA) was melt-blended with poly(p-vinyl phenol) (PVPh) using a two-roll mill, and the miscibility between PLLA and PVPh and degradation of... |
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| SubjectTerms | Applied sciences Chemical reactions and properties Degradation Exact sciences and technology Heat resistance improvement Miscible blend Organic polymers Physicochemistry of polymers Poly( l-lactide) Polymer blend |
| Title | Miscibility and hydrolytic degradation in alkaline solution of poly( l-lactide) and poly( p-vinyl phenol) blends |
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