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11.
A series of novel block polymers of polyurethane (PU) and chitosan have been prepared in two steps. The first step is the preparation of PU prepolymer, obtained from polytetramethylene oxide glycol (PTMO, Mn = 1000), isophrone diisocyanate (IPDI), and 2,2′-dimethylol propionic acid (DMPA), followed by ionizing PU prepolymer with triethylamine (TEA). The second step involves PU chain-extended by water-soluble chitosan of low molecular weight (Mn = 5000) by self-emulsion polymerization method. The sizes of the latex particles, morphology, and copolymer architecture have been characterized by dynamic light scattering (DLS), general tensile test, infrared spectroscopy (IR), surface contact angle measurement, and transmission electron microscopy (TEM). Furthermore, it shows that the addition of chitosan remarkably increases anticoagulative property of PU elastomers confirmed by the recalcification time. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
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Kai Stürken 《真空研究与实践》1996,8(2):78-82
The production of the polymer polyvinylchloride (PVC) emits a high amount of waste gas. The recovery of the evaporated base product vinylchoridemonomer (VC) is an important aspect for the economics of the whole process. Membrane and vacuum technology improve the efficiency and the economics of the recovery process considerably. 相似文献
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The kinetics of the methanation of carbon dioxide was investigated using an alumina supported Ni-La2O2 catalyst in a differential and integral reactor. In the differential reactor the molar ratio of H2 to CO2 was varied from 0.6 to 30. In the integral reactor the rates were measured with up to 90% conversion. Both reactor tests were carried out at temperatures between 513 and 593 K. The experimental results were described by a Langmuir-Hinshelwood type equation. The kinetics can be explained by assuming equilibrium of dissociative carbon dioxide and hydrogen adsorption, and assuming hydrogenation of surface carbon as the rate determining step. 相似文献
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This investigation focuses on slow, isothermal, two-phase flow of gas bubble suspensions in Separan solutions, prepared with the help of a sodium borohydride blowing agent at room temperature. The total residence time in these experiments is much smaller than characteristic times for growth or rise of bubbles. The variation of bubble volume fraction across a narrow gap between two planes, is recorded at two locations along the flow direction. This is done with a Cesium gamma-radiation source focused on a region of area.012 cm2 in the flow plane, and a Sodium iodide detector across the channel yielding a resolution of.01 over the range of void fractions investigated from.02 to.08. This measurement allows us to identify conditions under which the two-phase flow may be described by a two fluid model with a uniform bubbly core and a bubble free wall layer. With this two phase flow structure, a relative viscosity equation for the suspension is used to compute an apparent viscosity. Such calculations indicate that the observed reduction in apparent viscosity for the two phase flow may be attributed to a bubbly core which is more shear thinning than the medium. The additional shear thinning factor for the suspension is related to the elasticity of the medium. 相似文献
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