应用化学
應用化學
응용화학
CHINESE JOURNAL OF APPLIED CHEMISTRY
2009年
10期
1129-1133
,共5页
刘焱龙%柯卓%尹立刚%石强%殷敬华
劉焱龍%柯卓%尹立剛%石彊%慇敬華
류염룡%가탁%윤립강%석강%은경화
反应共混%增容%接枝物%乙烯辛烯共聚物%聚苯乙烯
反應共混%增容%接枝物%乙烯辛烯共聚物%聚苯乙烯
반응공혼%증용%접지물%을희신희공취물%취분을희
reactive blend%compatibilization%graft copolymer%polyethylene octane copolymer%polystyrene
采用新型双路易斯酸,三甲基氯硅烷和三氯化铟为催化剂引发傅氏烷基化反应,实现了乙烯辛烯共聚物(POE)和聚苯乙烯(PS)共混物的原位增容. 红外光谱的结果验证了接枝物的存在. 用扫描电子显微镜观察了反应共混物和简单物理共混物的形态, 前者分散相的尺寸小于1 μm,后者分散相的尺寸一般为3~4 μm. 原位生成的接枝物(PS-g-POE)起到相容剂的作用,增容后材料的力学性能得到较明显的提升. 如:当m(POE):m(PS)=40:60 时,与相同组成的物理共混物POE/PS相比,其悬臂梁冲击强度由1.9 kJ/m~2增加至9.7 kJ/m~2,断裂伸长率由3.4%提高至46.3%. 增容后的共混物低频区的复数粘度升高,表明POE、PS间相互作用增加.
採用新型雙路易斯痠,三甲基氯硅烷和三氯化銦為催化劑引髮傅氏烷基化反應,實現瞭乙烯辛烯共聚物(POE)和聚苯乙烯(PS)共混物的原位增容. 紅外光譜的結果驗證瞭接枝物的存在. 用掃描電子顯微鏡觀察瞭反應共混物和簡單物理共混物的形態, 前者分散相的呎吋小于1 μm,後者分散相的呎吋一般為3~4 μm. 原位生成的接枝物(PS-g-POE)起到相容劑的作用,增容後材料的力學性能得到較明顯的提升. 如:噹m(POE):m(PS)=40:60 時,與相同組成的物理共混物POE/PS相比,其懸臂樑遲擊彊度由1.9 kJ/m~2增加至9.7 kJ/m~2,斷裂伸長率由3.4%提高至46.3%. 增容後的共混物低頻區的複數粘度升高,錶明POE、PS間相互作用增加.
채용신형쌍로역사산,삼갑기록규완화삼록화인위최화제인발부씨완기화반응,실현료을희신희공취물(POE)화취분을희(PS)공혼물적원위증용. 홍외광보적결과험증료접지물적존재. 용소묘전자현미경관찰료반응공혼물화간단물리공혼물적형태, 전자분산상적척촌소우1 μm,후자분산상적척촌일반위3~4 μm. 원위생성적접지물(PS-g-POE)기도상용제적작용,증용후재료적역학성능득도교명현적제승. 여:당m(POE):m(PS)=40:60 시,여상동조성적물리공혼물POE/PS상비,기현비량충격강도유1.9 kJ/m~2증가지9.7 kJ/m~2,단렬신장솔유3.4%제고지46.3%. 증용후적공혼물저빈구적복수점도승고,표명POE、PS간상호작용증가.
A new type of combined catalyst of Lewis acids, Me_3SiCl and InCl_3·4H_2O, that can catalyze Friedel-Crafts alkylation reaction between POE and PS in the molten state was studied. The existence of grafted copolymer was testified by FTIR. SEM micrographs show that the size of the domains was decreased from 3~ 4 μm to less than 1 μm when the combined catalyst was added. Because the in-situ generated PS-g-POE copolymer could act as a compatibilizer in the blending system, the mechanical properties of the reacted blends were improved notably compared to that of the physical blends. For example, after compatibilization, the Izod impact strength of the m(POE)∶ m(PS) blend (40∶ 60) was increased from 1.9 kJ/m~2 to 9.7 kJ/m~2 and its elongation at break increased from 3.4% to 46.3%. The complex viscosity of the reacted blends within the low frequency range showed a higher value than that of the physical blends, indicating the increased interactions between POE and PS.