中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Thermoresponsive behavior of an LCST-type polymer based on a pyrrolidone structure in aqueous solution

文献类型:期刊论文

作者Lai, Hengjie1,2; Chen, Guangtao3; Wu, Peiyi1,2; Li, Zichen3
刊名SOFT MATTER
出版日期2012
卷号8期号:9页码:2662-2670
ISSN号1744-683X
DOI10.1039/c2sm06779j
英文摘要Poly(3-ethyl-N-vinyl-2-pyrrolidone) (C2PVP) is a new type of thermoresponsive polymer which exhibits phase separation in water above the lower critical solution temperature (LCST) at about 26 degrees C. The thermoresponsive mechanism of C2PVP during the heating-cooling cycle has been investigated by means of temperature-dependent FTIR in combination with a two-dimensional correlation (2Dcos) technique and density functional theory (DFT) calculations. Compared with a secondary-amide thermoresponsive polymer such as poly(N-isopropyl acrylamide) (PNIPAM), the unusual phenomenon of an asymmetrical-to-symmetrical transition of the C=O peak shape is observed in the conventional IR spectra of tertiary-amide polymer C2PVP. 2Dcos results confirmed that two species of C=O groups (C=O center dot center dot center dot 2D(2)O and C=O center dot center dot center dot D2O) mainly coexist at the initial heating, and they change to the other two C=O groups involving the free C=O and C=O center dot center dot center dot DOD center dot center dot center dot O=C after heating, with the latter predominant above the LCST. A slight hysteresis is observed in the cooling process attributed to the existence of a weak "crosslinking'' point originating from the structure of C=O center dot center dot center dot DOD center dot center dot center dot O=C. Based on 2Dcos results, the dehydration process of different groups could be described in the following order: ethyl groups > C=O groups > CH2 groups in ring (">'' means prior to), and the reversible sequence is observed during hydration process. In PNIPAM system, CH2 groups usually change prior to C=O groups, while for C2PVP the dehydrated rate of CH2 groups (in ring) lags behind that of C=O groups because of the steric hindrance of pyrrolidone structures. It is worth noting that cononsolvency of C2PVP can be found in water/methanol mixed solvents. The LCST of C2PVP in water/methanol mixture shifts from 29.5 to 16 degrees C as the methanol volume fraction reaches 50% and the phase separation totally disappears when the content of methanol is higher than 60%.
语种英语
WOS记录号WOS:000300048300013
出版者ROYAL SOC CHEMISTRY
源URL[http://ir.iccas.ac.cn/handle/121111/48089]  
专题中国科学院化学研究所
通讯作者Wu, Peiyi
作者单位1.Fudan Univ, Dept Macromol Sci, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
2.Fudan Univ, Adv Mat Lab, Shanghai 200433, Peoples R China
3.Peking Univ, Coll Chem & Mol Engn, Dept Polymer Sci & Engn, Key Lab Polymer Chem & Phys,Minist Educ,BNLMS, Beijing 100871, Peoples R China
推荐引用方式
GB/T 7714
Lai, Hengjie,Chen, Guangtao,Wu, Peiyi,et al. Thermoresponsive behavior of an LCST-type polymer based on a pyrrolidone structure in aqueous solution[J]. SOFT MATTER,2012,8(9):2662-2670.
APA Lai, Hengjie,Chen, Guangtao,Wu, Peiyi,&Li, Zichen.(2012).Thermoresponsive behavior of an LCST-type polymer based on a pyrrolidone structure in aqueous solution.SOFT MATTER,8(9),2662-2670.
MLA Lai, Hengjie,et al."Thermoresponsive behavior of an LCST-type polymer based on a pyrrolidone structure in aqueous solution".SOFT MATTER 8.9(2012):2662-2670.

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来源:化学研究所

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