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581.
To develop an efficient CO2 reduction catalyst, hybridizing a molecular catalyst and a porous coordination polymer (PCP) is a promising strategy because it can combine both advantages of the precise reactivity control of the former and the CO2 adsorption property of the latter. Although several PCP hybrid catalysts have been reported to date, the CO2 sorption behavior and the CO2 reduction reactivity have been investigated separately, and the CO2 enrichment during the catalysis is still unclear. We report CO2 photoreduction under different temperatures and pressures using a PCP-RuII complex hybrid catalyst. The product selectivity (CO or HCOOH) varied depending on the reaction conditions. The altered selectivity could be interpreted in terms of the CO2 capture in the micropores of a PCP.  相似文献   
582.
The γ-ray-induced copolymerization of ethylene and vinyl chloride with the use of liquid carbon dioxide as a solvent was studied under a total pressure of 400 kg/cm2, with a dose rate of 2.5 × 104 rad/hr at 30°C. A rubberlike, sticky polymer is obtained when the molar concentration of vinyl chloride is less than 30% in the monomer mixture, and the polymer is a white powder at higher concentrations of vinyl chloride. Infrared, x-ray, and differential thermal analyses confirm that the polymerization products are noncrystalline, true random copolymers. The rate of copolymerization decreases markedly when a small amount of vinyl chloride is added to ethylene monomer. In the range of vinyl chloride concentration higher than 5%, however, the rate and the molecular weight of copolymer increase with increasing concentration of vinyl chloride. It has been concluded from kinetic considerations based on these results that the rate of initiation increases proportionally with the concentration of vinyl chloride. Further, the growing chain radicals are shown to be deactivated by the cross-termination reaction between the radicals with terminal unit of ethylene and vinyl chloride, and no transfer reaction occurs.  相似文献   
583.
Summary: A novel quantitative method using isothermal titration calorimeter (ITC) for the estimation of the distribution of carboxyl groups within polymer particles has been proposed. The method has been employed to clarify the difference in the distribution between the particles prepared by batch emulsion copolymerization of styrene and methacrylic acid under inefficient and efficient stirring conditions. At inefficient stirring, monomer was floating as a layer on the aqueous medium, whereas at efficient stirring, the monomer phase was dispersed as droplets. Under inefficient stirring, methacrylic acid (MAA) polymerized faster than styrene (S) due to a slower diffusion rate of S than MAA into the aqueous medium, while under efficient stirring, S and MAA copolymerized at similar rates. ITC measurement showed that under inefficient stirring, the carboxyl groups were distributed mainly in the center of the particles, and their number decreased toward the surface. On the other hand, under efficient stirring, carboxyl groups were distributed homogeneously inside the particle.  相似文献   
584.
A main goal for manufacturing systems is to shorten lead‐time for the development of new products. An important challenge is to make sound decisions at early stages of product development where committed costs are low which leads us to obtain a lower total cost. This could mean that incurred costs are higher in the beginning where more work has to be done in terms of learning the market, developing the product and the production system. An important feature is to avoid changes at later stages where the incurred costs are high. The stereolithography using photo curable liquid resin is important for the manufacturing. The technology based on the stereolithography has been widely accepted due to the phenomena of spreading “Information Technology (IT)” and three‐dimensional computer aided design (3D CAD) system. The stereolithography technique has become very popular in the field of automotive, home‐electronics industries. In this paper the photo curable liquid resins for the stereolithography system are reviewed.  相似文献   
585.
InxGa1-xAs (x = 0.045) ternary bulk crystals were grown on GaAs seeds from an In–Ga–As solution by the temperature-difference method modified to rotate a growth ampoule. The effect of ampoule rotation on the profiles of the composition and the growth rate were investigated. The In compositional profiles were uniform irrespective of the ampoule rotation. On the other hand, the growth rate at the center of the crystal increased from 40 μm/h at 0 rpm to 55 μm/h at 100 rpm. The profile of growth rate changed from concave to convex toward the seed due to the ampoule rotation. Flow patterns and compositional profiles in the solution were simulated by solving four equations: Navier-Stokes, continuity, energy, and solute diffusion. The ampoule rotation enhanced the transportation of As component from the GaAs feed toward the seed at the central region in the solution. This led to the increase of the growth rate.  相似文献   
586.
587.
An enantiopure 1,2-diamine having two phenolic hydroxy groups was synthesized, and attached to chloromethylated poly(styrene) through a benzyl ether linkage. The polymer-supported Ru precatalysts were prepared from the polymeric chiral 1,2-diamine and RuCl2/BINAP complex. In the presence of t-BuOK the polymeric catalyst system worked well in asymmetric hydrogenation of aromatic ketones in a mixed solvent of 2-propanol and DMF. The insoluble polymeric catalyst was readily separated from the reaction mixture and reused at least several times without loss of the catalytic activity.  相似文献   
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