首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Synthesis, Characterization, and Pickering Emulsifier Performance of Anisotropic Cross-Linked Block Copolymer Worms: Effect of Aspect Ratio on Emulsion Stability in the Presence of Surfactant
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Synthesis, Characterization, and Pickering Emulsifier Performance of Anisotropic Cross-Linked Block Copolymer Worms: Effect of Aspect Ratio on Emulsion Stability in the Presence of Surfactant

机译:各向异性交联嵌段共聚物蠕虫的合成,表征和皮克林乳化剂性能:纵横比在表面活性剂存在下对乳液稳定性的影响

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Reversible addition-fragmentation chain transfer (RAFT) aqueous dispersion polymerization is used to prepare epoxy-functional PGMA-P(HPMA-stat-GlyMA) diblock copolymer worms, where GMA, HPMA, and GlyMA denote glycerol monomethacrylate, 2-hydroxypropyl methacrylate, and glycidyl methacrylate, respectively. The epoxy groups on the GlyMA residues were ring-opened using 3-amino-propyltriethoxysilane (APTES) in order to cross-link the worm cores via a series of hydrolysis-condensation reactions. Importantly, the worm aspect ratio can be adjusted depending on the precise conditions selected for covalent stabilization. Relatively long cross-linked worms are obtained by reaction with APTES at 20 degrees C, whereas much shorter worms with essentially the same copolymer composition are formed by cooling the linear worms from 20 to 4 degrees C prior to APTES addition. Small-angle X-ray scattering (SAXS) studies confirmed that the mean aspect ratio for the long worms is approximately eight times greater than that for the short worms. Aqueous electrophoresis studies indicated that both types of cross-linked worms acquired weak cationic surface charge at low pH as a result of protonation of APTES-derived secondary amine groups within the nanoparticle cores. These cross-linked worms were evaluated as emulsifiers for the stabilization of n-dodecane-in-water emulsions via high-shear homogenization at 20 degrees C and pH 8. Increasing the copolymer concentration led to a reduction in mean droplet diameter, indicating that APTES cross-linking was sufficient to allow the nanoparticles to adsorb intact at the oil/water interface and hence produce genuine Pickering emulsions, rather than undergo in situ dissociation to form surface-active diblock copolymer chains. In surfactant challenge studies, the relatively long worms required a thirty-fold higher concentration of a nonionic surfactant (Tween 80) to be displaced from the n-dodecane-water interface compared to the short worms. This su
机译:可逆添加 - 碎片链转移(筏)水分散聚合用于制备环氧官能的PGMA-P(HPMA-Stat-Glyma)二嵌段共聚物蠕虫,其中GMA,HPMA和Glyma表示甘油单甲基丙烯酸酯,2-羟丙基丙烯酸酯,和甲基丙烯酸缩水甘油酯。使用3-氨基 - 丙基三乙氧基硅烷(Aptes)进行甘氨酸残基上的环氧基团,以通过一系列水解 - 缩合反应将蠕虫核心交联。重要的是,蠕虫纵横比可以根据选择的精确条件来调节,以便共价稳定化。通过在20℃下的脂肪反应获得比较长的交联蠕虫,而通过在APTES添加之前通过将线性蠕虫从20至4℃冷却直接蠕虫来形成具有基本相同的共聚物组合物的更短的蠕虫。小角度X射线散射(萨克斯)研究证实,长蠕虫的平均纵横比大约比短蠕虫大约八倍。含水电泳研究表明,由于纳米颗粒内的Aptes衍生的仲胺基团质量,两种类型的交联蠕虫在低pH下获得弱阳离子表面电荷。将这些交联蠕虫评价为乳化剂,用于通过高剪切均质化在20℃和pH 8中稳定N-十二烷 - 水乳液。增加共聚物浓度导致平均液滴直径的减少,表明易于交联足以使纳米颗粒在油/水界面上的完整性,因此产生真正的皮克林乳液,而不是原位离解形成表面活性二嵌段共聚物链。在表面活性剂攻击性研究中,相对长的蠕虫需要与短蠕虫相比,从N-十二烷 - 水界面移位的非离子表面活性剂(TWEEN 80)所需的3倍浓度。这个su

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