Complete hydrogenation of d-galactose and l-arabinose mixtures on a Ru/C catalyst was achieved with excellent selectivities exceeding 95?%. No unexpected effects of temperature and pressure were observed. A detailed kinetic model was derived to describe the simultaneous hydrogenation of the monomeric sugars. 相似文献
The vacuum pressure swing adsorption (VPSA) method, as an alternative way to separate the CH4/N2 mixture, was adopted to purify methane from coal mine methane. The performance of the VPSA process was investigated experimentally and theoretically with a reactivated carbon molecule sieve as the adsorbent. The computer calculations were compared to the experimental data. The concentrated methane with 79% purity could be collected directly during the high-pressure adsorption step with 93% recovery and 0.0720 mL·g–1·min–1 productivity, when the composition of raw gas was 10/90 vol% CH4/N2, which is of great significance for the utility of low quality energy gas. 相似文献
We have investigated 4‐halopyridines as selective, tunable, and switchable covalent protein modifiers for use in the development of chemical probes. Nonenzymatic reactivity of 4‐chloropyridine with amino acids and thiols was ranked with respect to common covalent protein‐modifying reagents and found to have reactivity similar to that of acrylamide, but could be switched to a reactivity similar to that of iodoacetamide upon stabilization of the positively charged pyridinium. Diverse, fragment‐sized 4‐halopyridines inactivated human dimethylarginine dimethylaminohydrolase‐1 (DDAH1) through covalent modification of the active site cysteine, acting as quiescent affinity labels that required off‐pathway catalysis through stabilization of the protonated pyridinium by a neighboring aspartate residue. A series of 2‐fluoromethyl‐substituted 4‐chloropyridines demonstrated that the pKa and kinact/KI values could be predictably varied over several orders of magnitude. Covalent labeling of proteins in an Escherichia coli lysate was shown to require folded proteins, indicating that alternative proteins can be targeted, and modification is likely to be catalysisdependent. 4‐Halopyridines, and quiescent affinity labels in general, represent an attractive strategy to develop reagents with switchable electrophilicity as selective covalent protein modifiers. 相似文献
Micro-mesoporous aluminosilicates based on ZSM-5 zeolite, obtained by a dual template method, as well as in the presence of a dual-functional template (i.e. a Gemini-type surfactant), were tested in the oxidation of furfural with hydrogen peroxide. Even substantial changes in acidity and porosity of the catalysts result in minor variations of selectivity towards the desired products. Application of the synthesized zeolite-based materials in the oxidation of furfural with hydrogen peroxide leads to formation of 2(5H)-furanone (yield up to 28.5%) and succinic acid (up to 19.5%) as the main C4 reaction products. The kinetic model developed previously to treat the results for oxidation of furfural over sulfated zirconia was able to describe the data also for micro-mesoporous aluminosilicates.
A catalytic after treatment system for lean HC-SCR was constructed of two different catalyst beds, e.g. of a Ag/alumina and
Cu-ZSM-5 catalyst (cascade concept). The improved activity especially at low temperature range was found to be due to the
synergetic effect of the two catalysts, which combines the transformation of the feed gas over Ag/alumina to such compounds
that are highly reactive towards N2 over Cu-ZSM-5. The effluent coming from the Ag/alumina bed was analysed by GC–MS along with the NO to N2 conversion over the whole system by GC. The results obtained from the GC–MS measurements revealed that hydrocarbon used as
a reducing agent is oxidised and that besides oxygenates also various N-containing hydrocarbons are formed over the Ag/Al2O3. 相似文献
The reduction of NO with octane under lean conditions was examined over gold supported on alumina and titania and over alumina supported bimetallic gold–silver catalysts. The silver loading was either 1.2 or 1.9 wt% whereas 0.3, 1 or 5 wt% gold was used. The catalysts were characterized by means of EDXS, N2-adsortion, UV–Vis and TEM to correlate recorded results with different preparation methods. UV–Vis measurements indicated that gold was present in the form of fine Au particles, single Au ions and small (Au)nδ+ clusters on the catalysts and silver was mainly present in the form of single Ag ions. The highest NO to N2 reduction activity was recorded over the 0.3Au–Al2O3 catalyst. The Au–TiO2 catalysts did not result in significant NO to N2 reduction. 相似文献
A novel series of diarylpyrimidine analogues (DAPYs) featuring a naphthyl moiety at the C4 position were designed, with all compounds exhibiting strong activity against wild‐type HIV‐1.