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胶束态下聚环氧乙烷、聚丁烯氧化物、聚环氧丙烷和十八烷基链的表观比容随温度的变化测量

Apparent Specific Volume Measurements of Poly(ethylene oxide), Poly(butylene oxide), Poly(propylene oxide), and Octadecyl Chains in the Micellar State as a Function of Temperature.

作者信息

Sommer Cornelia, Pedersen Jan Skov, Stein Paul C

机构信息

Department of Chemistry, University of Aarhus, Langelandsgade 140, DK-8000 Aarhus C, Denmark.

出版信息

J Phys Chem B. 2004 May 20;108(20):6242-9. doi: 10.1021/jp036963c.

DOI:10.1021/jp036963c
PMID:18950107
Abstract

Apparent specific densities of aqueous solutions of the diblock copolymers C18(EO)100, C18(EO)20, and (EO)92(BO)18 and the triblock copolymers (EO)25(PO)40(EO)25 and (EO)21(PO)47(EO)21 in the micellar state have been measured over a temperature range from 10 to 90 degrees C at concentrations between 1% and 5%, using an oscillating tube densitometer. From these measurements, apparent specific volumes of poly(ethylene oxide) (PEO), poly(propylene oxide) (PPO), poly(butylene oxide) (PBO), and octadecane in the micellar state have been determined. The composition of the block copolymers was checked by NMR spectroscopy. Results were compared with published data for the polymers and bulk values for octadecane, respectively. The apparent specific density of PEO chains in the dissolved state was also measured for PEG4600 solutions at different concentrations and compared with results in the micellar state. The results presented in the paper are crucial in connection with analysis and modeling of small-angle X-ray scattering (SAXS) data from polymer and block copolymer micellar systems. PEO and PPO have a relatively low apparent partial specific volume in water at low temperatures. It is associated with water molecules making strong hydrogen bonds with the oxygen atoms on the polymer backbone. These water molecules gradually become disordered when the temperature is increased and the polymer apparent specific volume increases. For PBO in the micellar cores of PBO-PEO block copolymer micelles and in PNiPAM microgels, pronounced temperature dependence with the same origin is also found. The application of the derived results for the apparent specific volume of PEO for deriving contrast factors is demonstrated and the results are used in the analysis of SAXS data for semidilute solutions of PEG4600 in a broad temperature range.

摘要

使用振荡管密度计,在10至90摄氏度的温度范围内,对浓度在1%至5%之间的二嵌段共聚物C18(EO)100、C18(EO)20和(EO)92(BO)18以及三嵌段共聚物(EO)25(PO)40(EO)25和(EO)21(PO)47(EO)21的胶束态水溶液的表观比密度进行了测量。通过这些测量,确定了胶束态下聚环氧乙烷(PEO)、聚环氧丙烷(PPO)、聚环氧丁烷(PBO)和十八烷的表观比容。通过核磁共振光谱法检查了嵌段共聚物的组成。分别将结果与聚合物的已发表数据和十八烷的本体值进行了比较。还测量了不同浓度的PEG4600溶液中溶解态PEO链的表观比密度,并与胶束态的结果进行了比较。本文给出的结果对于分析和模拟来自聚合物和嵌段共聚物胶束体系的小角X射线散射(SAXS)数据至关重要。在低温下,PEO和PPO在水中的表观偏比容相对较低。这与水分子与聚合物主链上的氧原子形成强氢键有关。当温度升高且聚合物表观比容增加时,这些水分子逐渐变得无序。对于PBO-PEO嵌段共聚物胶束的胶束核中的PBO以及聚N-异丙基丙烯酰胺(PNiPAM)微凝胶中的PBO,也发现了具有相同起源的明显温度依赖性。展示了将PEO表观比容的推导结果应用于推导对比度因子,并将结果用于分析宽温度范围内PEG4600半稀溶液的SAXS数据。

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