采用大单体法合成梳型表面活性剂聚(苯乙烯-co-马来酸酐)-g-(聚乙二醇单甲醚)(St—MAMPEG).首先以N,N-二甲基甲酰胺(DMF)为溶剂,对甲基苯磺酸(PTSA)为催化剂,马来酸酐(MA)与聚乙二醇单甲醚(MPEG)酯化反应制备马来酸单聚乙二醇单甲醚酯大分子单体(MAMPEG);采用正交试验方法考察了溶剂用星、催化剂用量和温度对酯化反应的影响.结果表明,最佳合成工艺为:m(DMF):m(MA+MPEG)=1:1,w(PTSA)=2%(对单体质量),反应温度120℃.然后利用MAMPEG大分子单体与苯乙烯(St)自由基共聚制备St—MAMPEG梳型表面活性剂.利用红外光谱(IR)和氢核磁共振(^1 HNMR)分析MAMPEG及St—MAMPEG的结构.测定了St—MAMPEG的水溶液表面张力、浊点和浓溶液流变行为l吉果表明:St—MAMPEG具有降低表面张力的能力,其临界聚集质量浓度(cac)为0.20g/L,表面张力(γcac)为43.57mN/m.当St—MAMPEG水溶液pH为3.4时,浊点为63.7℃;pH为7.0时,在100℃以下无混浊现象.
Comb-shaped surfactant poly(styrene-co-maleic anhydride)-g-(poly(ethylene glycol) monomethyl ether) (St-MAMPEG) was prepared by macromonomer approach. First, the poly(ethylene glycol) mono- methyl ether maleate macromonomer (MAMPEG) was obtained by esterification of MPEG with MA using N, N-dimethylformamide (DMF) as solvent and p-toluene sulfonic acid (PTSA) as catalyst. The effects of solvent dosage, catalyst amount and temperature on the esterification were investigated through orthogonal experiments. The results showed the optimal synthesis technology: m(DMF): m(MA+MPEG)=1: 1, w(PTSA)=2% (on the mass of monomer), reaction temperature was 120 ℃. Then, the comb-shaped surfactant St-MAMPEG was prepared by radical copotymerization of MAMPEG and styrene (St). The structures of MAMPEG and St-MAMPEG were analyzed by infrared spectroscopy (IR) and 'H nuclear magnetic resonance(^1H NMR). The surface tension, cloud point and the rheological properties of the aqueous surfactant solutions were investigated. The results indicated that St-MAMPEG could decrease the surface tension, and its critical aggregation concentration (cac) and surface tension at cac (yooo) were 0.20 g/L and 43.57 mN/m, respectively. The cloud point of the aqueous solution in pH of 3.4 was 63.7 %. There was no appearance of cloud point below 100 % when the pH of solution was 7.0.