甲基丙烯酸

The polymethyl methacrylate material with super-hydrophobic surface of the invention is prepared in the following steps: 1 the polymethyl methacrylate material is first put into diamine solution, so that the ester group on the surface of the material has ammonolysis reaction with diamine molecules; 2 and then, the product of the step 1 is put into long chain fatty acid solution to be treated and the solvent is volatilized, so as to obtain the polymethyl methacrylate material with super-hydrophobic surface.

本发明具有超疏水表面的聚甲基丙烯酸甲酯材料，是按照如下步骤进行制备的：1将聚丙烯酸甲酯材料先置于二胺溶液中使聚丙烯酸甲酯材料表面的酯基与二胺分子发生氨解反应；2然后，将其置于长链脂肪酸溶液中进行处理，挥发掉溶剂，得到具有超疏水表面的聚甲基丙烯酸甲酯材料。

Results indicate that as the molecular mass of polyethylene glycol increases, the conductance is increased obviously, and the surface tension is decreased from 36.28 mN/m to 31.30 mN/m, while the cloud point is increased from 39.6 ℃ to 58.9 ℃. Their emulsifying abilities to BA, MMA and BMA are superior to that of OP-10, and the surfactants is homopolymerize or copolymerize with acrylate at 70 ℃ under the initiation of AIBN.

结果表明，随聚乙烯醇分子量的增加，非离子表面活性剂的电导率显著增加、表面张力由36.28 mN/m降低至31.30 mN/m、浊点由39.6 ℃增加至58.9 ℃，对丙烯酸丁酯、甲基丙烯酸甲酯和甲基丙烯酸丁酯的乳化能力均优于常用乳化剂OP-10，以AIBN作引发剂在70 ℃下既能均聚又可与丙烯酸酯进行共聚反应。

The title nano-sized polymeric microgels were synthesized by emulsion polymerization method,using divinyl benzene as crosslinking agent and methyl methacrylate,hydroxyl ethyl methacrylate,butyl acrylate as monomers.

通过乳液聚合的方法，以二乙烯基苯为交联剂，用甲基丙烯酸甲酯、甲基丙烯酸-β-羟乙酯、丙烯酸丁酯等丙烯酸酯类单体合成纳米尺寸的聚合物微凝胶粒子。

The article adopted the method of orthogonal design using Polyethylene Glycol and Methacrylic Acid to esterify Polythylene-glycol-mono Methacrylate, then using PMA, MAA and Methacrylic Acid Sulfonic Sodium as raw material to synthesize Polycarboxylic type water-reducer.

用正交实验法研究了聚乙二醇和甲基丙烯酸酯化合成聚乙二醇单甲基丙烯酸酯的合成工艺，以该酯化物与MAA和甲基丙烯酸磺酸钠为原料，在引发剂的作用下合成聚羧酸系减水剂。

The amphiphilic copolymer poly (MAA-SMA-PEGMA) was synthesized by the conventional free-radical copolymerization of methacrylic acid, stearyl acryate and poly methacrylate monomers.

利用功能性单体甲基丙烯酸、甲基丙烯酸十八烷基酯和聚乙二醇甲基丙烯酸酯通过常规自由基无规共聚反应，合成了两亲性共聚物Poly(MAA-SMA-PEGMA)。

In chapter four, molecular imprinting polymers against amino acid derivatives utilizing 2-VP+AM as combined functional monomer and trimethylolpropane trimethacrylate as tribasic cross-linker were prepared and result was compared with those with the same amino acid derivative as the imprinted molecules utilizing ethyleneglycol dimethacrylate as dibasic cross-linker. It was found that cross-link intensity of the molecular imprinting polymer is higher when TRIM was utilized and baseline separation for the imprinted molecule could be achieved. When TRIM was utilized as cross-linker more molecule is imprinted during the polymerization.

第四章采用2-乙烯基吡啶+丙烯酰胺复合功能单体，考察了三元交联剂三甲氧基丙烷三甲基丙烯酸酯烙印氨基酸衍生物的情况，并与二元交联剂乙二醇二甲基丙烯酸酯烙印相同氨基酸衍生物的情况进行了对比，发现三甲氧基丙烷三甲基丙烯酸酯交联剂在较小的用量下就可使分子烙印聚合物达到足够的交联度，实现烙印分子的基线分离。

A novel method combining a conventional free-radical solution polymerization with a chemical saponification was used to synthesize a, cu-dicarboxyl terminated oligo s with molecular weight below 1500. Here, cn-carboxyl terminated oligo s were firstly synthesized by the free-radical polymerization in THF, where 4,4'-azobis(4-cyanovaleric acid) was used as initiator, thioglycolic acid as chain transfer agent, then CTBMA were transformed into di-CTBMA via saponifying CTBMA in dioxane/H_2O/KOH solution.

利用传统自由基聚合法，在四氢呋喃溶液中自由基引发聚合甲基丙烯酸丁酯单体而得到w-羧基-甲基丙烯酸丁酯低聚物(分子量在1500左右)；利用CTBMA 末端酯基的反应特性，在二氧六环／水／KOH混合溶液中皂化CTBMA，使之转化为a ，w-羧基甲基丙烯酸丁酯低聚物；研究了溶剂的类别、反应时间等反应条件对皂化产物结构的影响；利用MALDI-TOF-MS及LSIMS对皂化各阶段产物进行了分析监测。

objective: to prepare the molecularly imprinted composite membranes with propofol as template.methods: with the ultraviolet light and initiator, template molecular propofol, functional monomer methacrylate and crosslinking agent ethylenegly-coldimethacrylate formed molecularly imprinted composite membrane through polymerization on the surface of polyvinyli-dene fluoride microporous membrane.inspection of the combination of template molecule and functional monomer, characterization of the membrane surface morphology with scanning electron microscopy.results: the morphology of composite membranes was well.propofol bonded to methylacrylic acid with hydrogen bond.conclusion: the method of ultraviolet light-struck is feasible for preparation of molecularly imprinted composite membranes with propofol as template.

目的：制备异丙酚分子印迹复合膜。方法：在紫外光照和引发剂的作用下，模板分子异丙酚、功能单体甲基丙烯酸和交联剂乙二醇二甲基丙烯酸酯在聚偏氟乙烯微孔滤膜表面聚合形成分子印迹复合膜，考察模板分子和功能单体的结合特性，用扫描电镜表征膜的表面形态。结果：复合膜形态良好，异丙酚和甲基丙烯酸以氢键的方式缔合。结论：用紫外光照射法可以制得异丙酚分子印迹复合膜。

The result indicated that MgO and α- methacrylic acid can together thicken epoxy, and the speed of thickening epoxy become quickly with the increasing content of MgO; when the ratio of MgO and α- methacrylic acid is 3:1, thickening epoxy have a better effect; the thickening mechanism: the terminal corboxyl group of α- methacrylic acid react with MgO, and it accompany with large numbers of heat, the heat can accelerate the reaction between the terminal corboxyl group with the secondary hydroxyl groups of epoxy, intermolecular hydrogen bonding which the water of above-mentioned formation result in and complex compound which format the metal atoms and carbonyl group complexing collective increase the viscosity of epoxy resin.

结果表明：MgO和α－甲基丙烯酸配合可增稠环氧树脂，随着MgO加入量的增加，环氧树脂增稠的速度加快；MgO与α－甲基丙烯酸为3：1时，增稠环氧树脂的效果较好；推测环氧树脂的增稠机理是α－甲基丙烯酸中的端羧基与氧化镁反应，放出热量促使其端羧基与环氧树脂中的仲羟基反应，上述反应生成水产生的氢键和羰基与氧化镁中的金属原子形成络合物共同导致环氧树脂的粘度增加。

MaterialsMethylmethacrylate, ethyl acrylate, acrylic acid and methacrylic acid (all A.R. grades, FirstChemical Reagent Factory, Tianjin, China) were puried bydistillation under reduced pressure and kept in therefrigerator.

物料甲基丙烯酸甲酯，丙烯酸乙酯，丙烯酸和甲基丙烯酸（所有机场铁路等级，第一化工试剂厂，天津，中国）的纯化减压蒸馏和留在refrigerator。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。