化工进展
化工進展
화공진전
CHEMICAL INDUSTRY AND ENGINEERING PROGRESS
2014年
11期
2882-2887
,共6页
许冰文%王红%何艳萍%肖小琴%孙彦琳
許冰文%王紅%何豔萍%肖小琴%孫彥琳
허빙문%왕홍%하염평%초소금%손언림
乳液%成核机理%乳化剂浓度%粒度分布
乳液%成覈機理%乳化劑濃度%粒度分佈
유액%성핵궤리%유화제농도%립도분포
emulsions%nucleation mechanism%surfactant concentration%particle size distribution
以苯乙烯(St)为单体、十二烷基硫酸钠(SDS)为乳化剂、过硫酸钾(KPS)为引发剂,重点研究了该乳液聚合体系中乳化剂浓度([S])对胶束成核和沉淀成核的影响规律。结果表明,当 SDS 浓度高于 CMC 时([S]≥8mmol/L),体系的成核以胶束成核为主;当[S]=2mmol/L 时,体系的成核以沉淀成核为主;当2mmol/L<[S]<8mmol/L时,体系同时以沉淀成核和胶束成核两种方式成核,且胶束成核所占的比例随着SDS浓度的增加而增大。研究了聚合反应过程中SDS浓度对单位体积水中乳胶粒个数(Np)的影响规律:当[S]≥8mmol/L时,Np∝[S]0.9;当[S]<8mmol/L时,Np∝[S]0.8。
以苯乙烯(St)為單體、十二烷基硫痠鈉(SDS)為乳化劑、過硫痠鉀(KPS)為引髮劑,重點研究瞭該乳液聚閤體繫中乳化劑濃度([S])對膠束成覈和沉澱成覈的影響規律。結果錶明,噹 SDS 濃度高于 CMC 時([S]≥8mmol/L),體繫的成覈以膠束成覈為主;噹[S]=2mmol/L 時,體繫的成覈以沉澱成覈為主;噹2mmol/L<[S]<8mmol/L時,體繫同時以沉澱成覈和膠束成覈兩種方式成覈,且膠束成覈所佔的比例隨著SDS濃度的增加而增大。研究瞭聚閤反應過程中SDS濃度對單位體積水中乳膠粒箇數(Np)的影響規律:噹[S]≥8mmol/L時,Np∝[S]0.9;噹[S]<8mmol/L時,Np∝[S]0.8。
이분을희(St)위단체、십이완기류산납(SDS)위유화제、과류산갑(KPS)위인발제,중점연구료해유액취합체계중유화제농도([S])대효속성핵화침정성핵적영향규률。결과표명,당 SDS 농도고우 CMC 시([S]≥8mmol/L),체계적성핵이효속성핵위주;당[S]=2mmol/L 시,체계적성핵이침정성핵위주;당2mmol/L<[S]<8mmol/L시,체계동시이침정성핵화효속성핵량충방식성핵,차효속성핵소점적비례수착SDS농도적증가이증대。연구료취합반응과정중SDS농도대단위체적수중유효립개수(Np)적영향규률:당[S]≥8mmol/L시,Np∝[S]0.9;당[S]<8mmol/L시,Np∝[S]0.8。
Formulation of latex with styrene (St),potassium persulfate (KPS) and sodium dodecyl sulfate (SDS) was investigated as a function of SDS surfactant concentration [S] to explore its nucleation mechanism. The results showed that micellar nucleation dominated the nucleation process when the concentration of SDS was ≥ 8 mmol/L; while,precipitation nucleation dominated the process at 2mmol/L. From 2mmol/L to 8mmol/L,both micellar nucleation and precipitation worked;and the contribution of micellar nucleation increased with the increase of the concentration of SDS. Additionally,the particle number of latex was calculated:Np∝[S]0.9 when [S] was≥8mmol/L;Np∝[S]0.8 when 8mmol/L≥[S]≥2mmol/L.