功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2014年
15期
15031-15035,15040
,共6页
毛扬帆%辛梅华%李明春%邢宇
毛颺帆%辛梅華%李明春%邢宇
모양범%신매화%리명춘%형우
壳聚糖%磺化%聚己内酯%胆固醇%单分子膜
殼聚糖%磺化%聚己內酯%膽固醇%單分子膜
각취당%광화%취기내지%담고순%단분자막
chitosan%sulfonated%poly(ε-caprolactone)%cholesterol%monolayer
制备聚己内酯改性 O-磺化壳聚糖(HSCS-g-PCL),用 FT-IR、EA 和1 H NMR 对产物进行表征,并研究其与胆固醇的混合单分子膜性质.结果表明,单组份 HSCS-g-PCL 单分子膜π-A 曲线为膨胀型,而混合单分子膜则转变为凝聚型并均具有明显 LE-LC相转变;随着胆固醇含量的增加,混合单分子膜的崩溃压和极限分子面积降低,最大压缩模量增大;胆固醇摩尔分数为0.6时两组份分子间作用力从相互排斥转为相互吸引,为0.8时,体系超额自由能Δ exc 最小,两组份间相容性最好,体系最稳定.
製備聚己內酯改性 O-磺化殼聚糖(HSCS-g-PCL),用 FT-IR、EA 和1 H NMR 對產物進行錶徵,併研究其與膽固醇的混閤單分子膜性質.結果錶明,單組份 HSCS-g-PCL 單分子膜π-A 麯線為膨脹型,而混閤單分子膜則轉變為凝聚型併均具有明顯 LE-LC相轉變;隨著膽固醇含量的增加,混閤單分子膜的崩潰壓和極限分子麵積降低,最大壓縮模量增大;膽固醇摩爾分數為0.6時兩組份分子間作用力從相互排斥轉為相互吸引,為0.8時,體繫超額自由能Δ exc 最小,兩組份間相容性最好,體繫最穩定.
제비취기내지개성 O-광화각취당(HSCS-g-PCL),용 FT-IR、EA 화1 H NMR 대산물진행표정,병연구기여담고순적혼합단분자막성질.결과표명,단조빈 HSCS-g-PCL 단분자막π-A 곡선위팽창형,이혼합단분자막칙전변위응취형병균구유명현 LE-LC상전변;수착담고순함량적증가,혼합단분자막적붕궤압화겁한분자면적강저,최대압축모량증대;담고순마이분수위0.6시량조빈분자간작용력종상호배척전위상호흡인,위0.8시,체계초액자유능Δ exc 최소,량조빈간상용성최호,체계최은정.
O-sulfonated chitosan-graft-poly(ε-caprolactone)(HSCS-g-PCL)was synthesiz- ed and the structure of it was characterized by FT-IR,1 H NMR and EA.The properties of mixed monolayers of HSCS-g-PCL and cho-lesterol were studied.Experimental results indicated that when cholesterol was added,the π-A isotherms of the HSCS-g-PCL monolayer turned from expand type into condensation type and had obvious LE-LC phase transi-tion.As the cholesterol molar ratio increased,collapse pressure and the limiting molecular area of mixed mono-layers decreased,meanwhile maximum compression modulus increased.The value of Δ exc changed from an re-pulsive interaction to an attractive interaction between HSCS-g-PCL and cholesterol with a critical point when cholesterol molar ration was 0.6.When molar ratio of cholesterol was 0.8,Δ exc of mixed monolayers was mini-mum and the mixed monolayer was the most stable.