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排序方式: 共有467条查询结果,搜索用时 31 毫秒
1.
H.-J. Sue E. I. Garcia-Meitin N. A. Orchard 《Journal of Polymer Science.Polymer Physics》1993,31(5):595-608
The fracture behavior of a core-shell rubber (CSR) modified epoxy is investigated using both fracture mechanics and microscopy tools. The CSR-modified epoxy is found to be toughened via numerous line-array cavitations of the CSR particles, followed by plastic flow of the epoxy matrix. The toughening effect via the above craze-like damage process is found to be as effective as that of the well-known widespread rubber cavitation/matrix shear yielding mechanisms. The conditions for triggering the craze-like damage appear to be both stress state and rubber concentration dependent. The type of rubber tougheners utilized also plays a critical role in triggering this rather unusual craze-like damage in epoxy systems. © 1993 John Wiley & Sons, Inc. 相似文献
2.
Rachel K. O'Reilly Maisie J. Joralemon Craig J. Hawker Karen L. Wooley 《Journal of polymer science. Part A, Polymer chemistry》2006,44(17):5203-5217
Block copolymer micelles and shell cross-linked nanoparticles (SCKs) presenting Click-reactive functional groups on their surfaces were prepared using two separate synthetic strategies, each employing functionalized initiators for the controlled radical polymerization of acrylate and styrenic monomers to afford amphiphilic block copolymers bearing an alkynyl or azido group at the α-terminus. The first route for the synthesis of the azide-functionalized nanostructures was achieved via sequential nitroxide-mediated radical polymerization (NMP) of tert-butyl acrylate and styrene, originating from a benzylic chloride-functionalized initiator, followed by deprotection of the acrylic acids, supramolecular assembly of the block copolymer in water and conversion of the benzylic chloride to a benzylic azide. In contrast, the second strategy utilized an alkynyl-functionalized reversible addition fragmentation transfer (RAFT) agent directly for the RAFT-based sequential polymerization of tetrahydropyran acrylate and styrene, followed by selective cleavage of the tetrahydropyran esters to give the α-alkynyl-functionalized block copolymers. These Click-functionalized polymers, with the functionality located at the hydrophilic polymer termini, were then self-assembled using a mixed-micelle methodology to afford surface-functionalized “Clickable” micelles in aqueous solutions. The optimum degree of incorporation of the Click-functionalized polymers was investigated and determined to be ca. 25%, which allowed for the synthesis of well-defined surface-functionalized nanoparticles after cross-linking selectively throughout the shell layer using established amidation chemistry. Functionalization of the chain ends was shown to be an efficient process under standard Click conditions and the resulting functional groups revealed a more “solution-like” environment when compared to the functional group randomly inserted into the hydrophilic shell layer. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5203–5217, 2006 相似文献
3.
采用氧化铝模板结合交流电沉积技术制备纯银纳米线, 然后通过化学还原方法, 并控制加入的金盐的量, 在已制备好的银线表面包裹不同厚度的金壳层, 得到具有核壳结构的Ag核Au壳复合纳米线. 采用电子显微镜(SEM, TEM)和表面增强拉曼光谱对该复合结构纳米线进行相关表征, 纳米线的表面形貌与加入的金盐的量有关. 以苯硫酚(TP)和对巯基苯胺(PATP)为探针分子, 研究了此类复合纳米线的表面增强拉曼散射效应. 并以PATP在金银纳米线表面吸附的表面增强拉曼光谱的差别为探针, 表征了复合纳米线表面金的包裹程度, 结果表明一定厚度的包裹程度可制备无针孔效应的核壳结构金银复合纳米线. 相似文献
4.
According to the new method of preparing core-shell nanospheres developed by our group, by using two monomers, 2-hydroxypropyl
methacrylate(HPMA) and vinyl acetate(VAc), two kinds of core-shell nanospheres with poly(ɛ-caprolactone) (PCL) as the core
and crosslinked poly(2-hydroxypropyl methacrylate) (PHPMA) or poly(vinyl acetate) (PVAc) as the shell were successfully prepared
under similar conditions. After degrading the PCL cores of the two kinds of nanospheres by lipase, the corresponding crosslinked
poly(methyl acrylic acid) hollow spheres and crosslinked poly(vinyl alcohol) hollow spheres were obtained. Results indicate
that the new method we proposed for preparing core-shell polymeric nanospheres via in-situ polymerization can be generalized to a certain extent, and it is suitable for many systems provided the monomer used is soluble
in water, while its corresponding polymer is insoluble in water.
Translated from Chemical Journal of Chinese University, 2006, 27(9): 1762–1766 [译自: 高等学校化学学报] 相似文献
5.
6.
H. -J. Sue E. I. Garcia Meitin D. M. Pickelman C. J. Bott 《Colloid and polymer science》1996,274(4):342-349
The fracture mechanisms of a high performance epoxy system modified with two types of preformed rigid core-shell particles (RCSP) were investigated. The use of the preformed RCSP anables the control of the dispersion of the toughener phase in the epoxy, which, in turn, allows the mechanical properties of the modified epoxy to be optimized. The toughening effect via the RCSP modification is found to be as good as that via the core-shell rubber modification. The moduli andT
g of these RCSP-modified epoxies are virtually unaltered via the RCSP modification, when compared with the neat epoxy resin equivalent. The toughening mechanisms in these toughened systems appear to be predominantly crack deflection, crack bifurcation, and microcracking. Approaches for effective toughening of high performance polymers via rigid polymers are discussed. 相似文献
7.
The preparation of polymer microcapsules of well defined size in the range of 10–50 μm with different shell thickness to
core diameter ratios is described. An aerosol of monodisperse droplets of a homogeneous ternary liquid system which contained
a hydrophobic component and a hydrophilic component dissolved in a high-volatile mutual solvent, was produced by dispersing
with a vibrating-orifice aerosol generator. After the evaporation of the solvent in a nitrogen atmosphere the particles demix
and form a two-phase droplet of core-shell type. These droplets were illuminated with UV light and polymerized to highly monodisperse
microcapsules with a solid polymer shell and a liquid core. The properties of the resulting particles (size, size distribution,
shell thickness, shape and surface characteristics) were investigated by scanning electron microscopy, Raman spectroscopy
on single optically levitated particles, and confocal Raman micro spectroscopy. The microcapsules were highly monodisperse
and have spherical shape.
Received: 24 July 1996 Accepted: 29 August 1996 相似文献
8.
Oi-lian Song Guang-zhao Zhang Chi Wu 《高分子科学》2007,(5):441-445
Using a core(142 nm)made of linear polystyrene(PS)chains as a seed,we further polymerized a thin layer of cross-linked PS shell(7 nm)on it in water to form a core-shell particle.Such a particle swells in toluene,which enables linear PS chains inside the core to gradually diffuse out through the porous shell.Using a combination of static and dynamic laser light scattering,we examined the chain diffusion process by following the change of the scattering intensity(i.e.the average molar mass of the particles).For the first time,we have revealed that the diffusion exhibits three stages.In the first stage,the chain diffusion through the shell is even faster than their translational diffusion in a dilute solution.The three stages respectively correspond to the change of the solution in the core from concentrated to semidilute and then from semidilute to dilute. 相似文献
9.
A triangular lattice model for pattern formation by core-shell particles at fluid interfaces is introduced and studied for the particle to core diameter ratio equal to 3. Repulsion for overlapping shells and attraction at larger distances due to capillary forces are assumed. Ground states and thermodynamic properties are determined analytically and by Monte Carlo simulations for soft outer- and stiffer inner shells, with different decay rates of the interparticle repulsion. We find that thermodynamic properties are qualitatively the same for slow and for fast decay of the repulsive potential, but the ordered phases are stable for temperature ranges, depending strongly on the shape of the repulsive potential. More importantly, there are two types of patterns formed for fixed chemical potential—one for a slow and another one for a fast decay of the repulsion at small distances. In the first case, two different patterns—for example clusters or stripes—occur with the same probability for some range of the chemical potential. For a fixed concentration, an interface is formed between two ordered phases with the closest concentration, and the surface tension takes the same value for all stable interfaces. In the case of degeneracy, a stable interface cannot be formed for one out of four combinations of the coexisting phases, because of a larger surface tension. Our results show that by tuning the architecture of a thick polymeric shell, many different patterns can be obtained for a sufficiently low temperature. 相似文献
10.
Mahboubeh Ghasemian Dazmiri Heshmatollah Alinezhad Zinatossadat Hossaini Ahmad R. Bekhradnia 《应用有机金属化学》2020,34(9):e5731
In this research, Fe3O4/ZnO magnetic core-shell nanoparticles (Fe3O4/ZnO MCNPs) were synthesized through a green method using Petasites hybridus rhizome water extract as a reducing and stabilizing agent. The morphology and size of the Fe3O4/ZnO MCNPs was identified by X-ray diffraction, scanning electron microscopy, and Energy-dispersive X-ray spectroscopy (EDX) analysis. The catalytic activity of the Fe3O4/ZnO MCNPs was evaluated in the efficient and green preparation of pyran derivatives in excellent yield using three-component reactions of dimedone, aldehydes, and malononitrile in ethanol at room temperature. The ability of some synthesized compounds to scavenge the 2,2-diphenyl-1-picrylhydrazyl radical was measured and the results proved this observation. Moreover, the antimicrobial activity of some synthesized compounds was proved by employing the disk diffusion test on Gram-positive and Gram-negative bacteria. The results for the disk diffusion test showed that compounds ( 4c, 4d, 4f and 4g ) prevented bacterial growth. 相似文献