聚合物乳液的稳定性

简要讨论了乳液稳定性的原理,综述了乳液配方、乳胶粒组成和结构对聚合物乳液电解质稳定性、机械稳定性、冻融稳定性和贮存稳定性的影响。     

Soap‐free emulsion copolymerization of perfluoroalkyl acrylates in the presence of a reactive surfactant

Soap‐free emulsion copolymerization of perfluoroalkyl acrylate (FA)/methyl methacrylate (MMA)/n‐butyl acrylate (n‐BA) was carried out in the presence of sodium 2‐acrylamide‐2‐methyl propanesulfonate (AMPSNa) as a reactive surfactant and potassium persulfate (KPS) as an initiator. An analysis of the effects of concentration of AMPSNa, KPS, FA as well as polymerization temperature on the kinetic features (rate of polymerization) and colloidal characteristics (mean particle diameter, particle disperse index, particle numbers, and surface charge density) was followed. NMR, FTIR, AFM, and fluorine‐selective electrode analysis were used to characterize the composition and morphology of the FA copolymers. Both AFM analysis and contact angle measurements strongly implied that the fluorinated segments migrated to the outmost surface and created films with lower surface energy. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 2438–2444, 2007     

20%单氰乳剂剂型研究

本文所叙述的单氰乳剂，是一种新的复配农药制剂。它不仅增效作用显著，对为害农作物的蚜虫和红蜘蛛有很强的杀灭作用；而且其剂型独特，为国内尚不多见的水包油型的复配农药新制剂－微乳剂。该制剂生产工艺简单，产品性能稳定，常温贮存一年，有效成分分解率低于１．５％；在６０℃至－５℃范围内，其产品均为均相透明的液体，且乳化性能十分优良。目前该品种已取得农药登记，正式投产。     

水性聚氨酯的合成及其改性的研究

研究了 n NCO/n OH、扩链剂 ( BD)及二羟甲基丙酸 ( DMPA)的含量对水性聚氨酯合成及涂膜性能的影响 ,确定了较佳的配方。并利用甲基丙烯酸酯类单体合成聚氨酯 -丙烯酸酯共聚复合乳液来改善水性聚氨酯的性能     

保护胶体稳定的丙烯酸酯乳液流变性

分别采用常规乳化剂和羟乙基纤维素为保护胶体制备丙烯酸酯乳液。通过TEM分别观察乳胶粒的形态。利用流变仪测定剪切速率（Ds）-剪切应力（τ）关系、剪切速率（Ds）-黏度（η）关系。结果表明：采用羟乙基纤维素为保护胶体制备的乳液与常规乳液具有不同结构，该结构使其乳液体系流变性能不同。在相同剪切速率下，保护胶体制备的丙烯酸酯乳液的剪切力明显大于常规乳液的剪切力，该乳液在一定剪切速率范围内有剪切稀化现象。     

丙烯酸酯无皂乳液的研究

在甲基丙烯酸甲酯和丙烯酸丁酯的无皂乳液体系中，加入适量的自制聚氨酯型反应性乳化剂(URE)，考察单体配比和有机溶剂对乳胶膜性能的影响，并研究了聚合物乳液的稳定性。结果表明：与传统乳液聚合体系相比，所合成的胶乳耐电解质、耐酸碱、耐有机溶剂的性能均好。     

Grafting poly(t‐butyl acrylate) to poly(allylamine) by inverse microemulsion radical polymerization: From comb‐polymer to amphiphilic shell crosslinked polymer nanocapsule

An interfacial grafting radical polymerization method for amphiphilic comb copolymer and shell crosslinked polymer nanocapsules was reported. Macropolyradicals on a water soluble long chain polyamine were generated with hydrogen peroxide in the water phase and subsequent grafting radical polymerization of a vinylic monomer at the water/oil interface proceeded at 65°C. In the presence of a crosslinker, the resulting graft copolymer formed a defined core‐shell structure with hydrophilic aqueous core functionalized by the polyamine and a hydrophobic crosslinked polymer shell. The structure of the core‐shell material was characterized by NMR, FTIR, DSC, TGA, SEM, TEM, and the mechanism of the graft polymerization is proposed. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1905–1911, 2007     

Does morphology stick? Tailored particle morphologies by swelling polymerization process

Structured dispersion particles suitable for pressure sensitive adhesives (PSA) were synthesized via swelling polymerization technique (EP 359562). Particles consisting of poly(n‐butyl acrylate) copolymerized with different types of carboxylic acids were used as seeds. The final particles were synthesized by swelling polymerization process, using 6 wt % styrene or 6 wt % methyl methacylate. The resulting particle morphology was analyzed by atomic force microscopy (AFM) and transmission electron microscopy (TEM). From previous works (Coll Surf A 2001, 183–185, 725–737; J Appl Polym Sci 2004, 91, 2610–2623) where two‐step emulsion polymerization was used on similar particles, it is expected that the particle morphology is affected by the polarity of the monomer used for swelling polymerization because of the phase compatibility (thermodynamic parameter). In this work, the seed particles used were always of a glass transition temperature (T_g) below polymerization temperature. The diffusion of the growing polymer chains from the swelling polymerization is therefore mainly affected by their own T_g and the influence of the carboxy groups on the chain length of the entering radicals (kinetic parameter). The different morphologies of the single particles are discussed qualitatively. The effects of reaction parameters are compared with the results given in the previous work. The structure of the corresponding dispersion films was characterized using AFM. Correlations to macroscopic properties such as the cohesive strength and peel adhesion to different substrates are discussed. The results are also compared with the application properties of the corresponding unmodified particles, statistical copolymers, and to blends with small sized PMMA or PS particles. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1444–1455, 2006     

肠溶型药物包衣用丙烯酸树脂的制备工艺

采用乳液聚合法制备肠溶型药物包衣用丙烯酸树脂,采用甲基丙烯酸与甲基丙烯酸甲酯作为共聚单体、过硫酸钾作为引发剂、十二烷基硫酸钠及OP-10复配作为乳化剂、苯乙烯的二聚体作为分子量调节剂、碳酸氢钠作为pH值调节剂,考察了乳化剂配比及用量、引发剂及分子量调节剂的用量、反应温度、加料方式、相比等因素的影响,最终确定了实验制备药物包衣用丙烯酸树脂的最佳条件。利用乌氏粘度计测定其相对分子量,并作了红外光谱测试,结果表明,乳液符合国家药典要求。该制备过程避免了有机溶剂的使用,有明显的经济和环保效益。     

冠醚化合物做为晶体生长的物理成熟剂

本文在制备AgBr八面体乳剂初液中,加入一系列不同量的1,7,10,16-四氧-4,13-二硫代杂环十八烷(2S-18-C-6),结果由于(2S-18-C-6)与银离子产生了络合,降低了乳剂成核的过饱和度,所得乳剂的颗粒大小与加入2S-18-C-6的量成正比。由于所得乳剂颗粒大小分布产生了变化,而使乳剂的光化学性质以及介电损耗也产生了规律性的变化。同时还发现,在乳剂成熟过程中,加入含杂质原子不同的冠醚化合物1,4,7,10,13,16-六氧环十八烷(18-C-6),1,7,10,16-四氧-4,13-二氮代杂环十八烷(2N-18-C-6),N-对甲苯磺酰基-7-氮杂-1,4,10,13-四氧硫杂环十六烷(NTsTTH)对晶体的物理成熟作用有很大差异,2S-18-C-6是很好的物理成熟剂,2N-18-C-6、NTsTTH是AgBr的溶剂,18-C-6的成熟作用很弱,说明冠醚化合物对AgBr的溶解成熟作用与其环上所含杂原子有关。