物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2013年
2期
341-345
,共5页
吴旭*%蔡晓新%王金本%杨惠%史学峰
吳旭*%蔡曉新%王金本%楊惠%史學峰
오욱*%채효신%왕금본%양혜%사학봉
聚集行为%NaCl%聚集体%刷型聚合物%调控
聚集行為%NaCl%聚集體%刷型聚閤物%調控
취집행위%NaCl%취집체%쇄형취합물%조공
Aggregation behavior%NaCl%Aggregate%Brush-like polymer%Control
两亲聚合物奇异的功能特性源于分子独特的骨架结构和在溶液中的自组装聚集行为.本文向以2-丙烯酰胺基-十二烷基磺酸(AMC12S)与2-丙烯酰胺基-2-甲基丙磺酸(AMPS)进行无规共聚所制备的AMPS-AMC12S刷型两亲聚合物溶液体系中引入不同用量的NaCl,采用稳态荧光、动态光散射(DLS)和透射电子显微镜(TEM)系统考察NaCl对聚合物聚集行为的调控作用.研究发现,聚合物结构中疏水侧链含量越低, NaCl对聚集行为的调控作用越强; NaCl浓度增加会明显降低聚合物的临界聚集浓度;与此同时,聚合物分子链自组装由分子间的聚集方式向分子内的聚集方式转变,形成的聚集形态由大型多分子聚集体变化为尺寸数百分之一的单聚体.
兩親聚閤物奇異的功能特性源于分子獨特的骨架結構和在溶液中的自組裝聚集行為.本文嚮以2-丙烯酰胺基-十二烷基磺痠(AMC12S)與2-丙烯酰胺基-2-甲基丙磺痠(AMPS)進行無規共聚所製備的AMPS-AMC12S刷型兩親聚閤物溶液體繫中引入不同用量的NaCl,採用穩態熒光、動態光散射(DLS)和透射電子顯微鏡(TEM)繫統攷察NaCl對聚閤物聚集行為的調控作用.研究髮現,聚閤物結構中疏水側鏈含量越低, NaCl對聚集行為的調控作用越彊; NaCl濃度增加會明顯降低聚閤物的臨界聚集濃度;與此同時,聚閤物分子鏈自組裝由分子間的聚集方式嚮分子內的聚集方式轉變,形成的聚集形態由大型多分子聚集體變化為呎吋數百分之一的單聚體.
량친취합물기이적공능특성원우분자독특적골가결구화재용액중적자조장취집행위.본문향이2-병희선알기-십이완기광산(AMC12S)여2-병희선알기-2-갑기병광산(AMPS)진행무규공취소제비적AMPS-AMC12S쇄형량친취합물용액체계중인입불동용량적NaCl,채용은태형광、동태광산사(DLS)화투사전자현미경(TEM)계통고찰NaCl대취합물취집행위적조공작용.연구발현,취합물결구중소수측련함량월저, NaCl대취집행위적조공작용월강; NaCl농도증가회명현강저취합물적림계취집농도;여차동시,취합물분자련자조장유분자간적취집방식향분자내적취집방식전변,형성적취집형태유대형다분자취집체변화위척촌수백분지일적단취체.
The extraordinary properties of amphiphilic polymers originate from their unique skeleton structures and the aggregation behavior of the polymer chains. In the present work, we introduced different amounts of NaCl into AMPS-AMC12S brush-like amphiphilic polymers synthesized via the statistical polymerization of 2-(acrylamido)-dodecanesulfonic acid (AMC12S) with 2-(acrylamido)-2-methylpropanesulfonic acid (AMPS), and investigated the effects of the NaCl on the aggregation behavior of the polymers, using steady-state fluorescence, dynamic light scattering, and transmission electron microscopy. The results showed that the effects of the salt were more intense for polymers with fewer side chains. As the NaCl concentration increased, the polymer chains associated at a lower critical concentration. The polymers tended to aggregate in an intrapolymer configuration, in preference to an interpolymer configuration; this resulted in the formation of smal er unimers, rather than giant multipolymer aggregates. The results described here provide an efficient approach for control ing the aggregation behavior of amphiphilic polymers, and have significance in advancing the design and control of functional aqueous systems, as wel as in promoting the development and application of novel polymers.