共查询到10条相似文献,搜索用时 265 毫秒
1.
The study of CCl4 adsorption shows that the increase of dispersion potential can increase the specific adsorption in pores up to 3 nm in size.
CCl4 , 3 .相似文献
2.
V. N. Romannikov N. V. Klueva N. N. Bobrov K. G. Ione 《Reaction Kinetics and Catalysis Letters》1976,5(2):217-222
The dependence of palladium distribution in zeolites on the temperature of thermal treatment has been established from the data on oxygen chemisorption and the statistical processing of electron micrographs. The influence of palladium distribution in zeolites on their catalytic activity towards the complete oxidation of benzene has been shown.
- . .相似文献
3.
Radical intermediates formed at 25°C in the presence and absence of oxygen during the photolysis of anthraquinone in aromatic, cyclic and aliphatic hydrocarbon solvents were trapped by 2,6-dichloronitrosobenzene, 2,6-dibromonitrosobenzene and 2,4,6-tribromonitrosobenzene. The resulting nitroxide radicals have been characterized in situ by ESR spectra.
: 2,6-, 2,6- 2,4,6-— , , 25°C. .相似文献
4.
P. V. Srinivasulu M. Adinarayana B. Sethuram T. Navaneeth Rao 《Reaction Kinetics and Catalysis Letters》1985,27(1):167-172
Kinetics of OsO4 catalyzed oxidation of chalcones by Ce4+ has been studied in aqueous acetic-sulfuric acid medium in the temperature range 313 to 338 K. The order in [oxidant] is zero while the order with respect to [substrate] and [catalyst] are each fractional. The rate of the reaction decreased with increase in percentage of acetic acid while [H+] had practically no effect on the rate The rates of various substituted chalcones (with substituents in the phenyl. ring attached to the moiety) are in the orderp-CH3>m-CH3>H>p-Cl>m-Cl>m-NO2>p-NO2. A mechanism in which formation of a cyclic ester between chalcone and OsO4 in a fast step followed by its decomposition in a rate-determining step is envisaged.
Ce4+, OsO4, - 313–338 . —, —. , [H+] . ( , : -CH3>-CH3>H>-Cl>-NO2>-NO2. , OsO4 , , .相似文献
5.
The effect of substituted hydroxybenzophenone, benzotriazole and organic metal complexes on the photooxidation of PP films has been studied. It has been established that NiDBTC added in 1.0 wt. % is the most effective photostabilizer.While in the case of other stabilizers there is a slight increase in the Co content even during the induction period, with the application of NiDBTC practically no oxidation can be observed before the stabilizer completely disappears. This means that NiDBTC inhibits the photooxidation of the polymer even in low concentration.
, - . , Ni, 1,0 . %. . , Ni , . , Ni .相似文献
6.
The oxidation of methane on supported chromia was studied at temperatures varying between 423 and 743 K and CH4/O2 ratios between 1 and 9 in a differential reactor. The main reaction products observed were carbon monoxide and formaldehyde. The rates of reaction obey a power law expression.
, 423 743 CH4/O2 1 9, . . .相似文献
7.
IR spectra of propylene adsorbed in CoO-MgO and CoO-MgO-MoO3 solid solutions show that a surface -complex with Co2+ ions is formed, strongly bonded in the former case and weakly in the latter. Thus, introduction of Mo strongly modifies the catalytic properties of Co2+ active centers. In the presence of oxygen, allylic species, aldehyde and carboxylate complexes appear.
, CoO-MgO CoO-MgO-MoO3 - Co2+, . , Mo Co2+. - .相似文献
8.
T. Borowiecki 《Reaction Kinetics and Catalysis Letters》1987,33(2):429-434
Experiments on the coking rates of variously prepared nickel catalysts on TiO2, Al2O3 and MgO in n-butane steam reforming show that changes in the relative coking rate at a rising steam excess in the gas phase depend mainly on the kind of support. The results obtained are accounted for by changes in the electron density at the site of nickel crystallite contact with the surface of various supports.
, TiO2, Al2O3 MgO, - , , , , , . .相似文献
9.
The hydrodesulfurization (HDS) of thiophene by nickel-molybdenum catalysts supported on alumina-zirconia has been investigated. The effect of varying the ratios of oxides in the support is to produce a minimum in the activity for HDS, and the coimpregnated catalysts are shown to be more active than the analogous co-precipitated catalysts.
(HDS) -, . HDS. , .相似文献
10.
The reactions of phenyl glycidyl ether (PGE) with phosphoric acid in three molar ratios have been studied by means of DSC alone. The results obtained from isothermal measurements are as follows:H=–91.0 kJ/mole PGE(1:1 molar ratio);H=–100.5 kj/mole PGE (1:2/3 molar ratio).The DSC curves obtained from dynamic experiments are multipeaked and giveHvalues higher than those obtained from isothermal measurements. These results can be explained by taking into account the acid concentration, the different reactivities of the hydrogens of the phosphoric acid and the possibility that secondary reactions occur.
Zusammenfassung Die Reaktion von Phenylglycidyläther (PGE) mit Phosphorsäure wurde bei drei verschiedenen molaren Verhältnissen allein mittels DSC untersucht. Isotherme Messungen ergaben folgende Werte:H=–91.0kJ/mol PGE (molares Verhältnis 1:1);H=–100.5 kJ/mol PGE (molares Verhältnis 3:2). Die bei dynamischen Experimenten erhaltenen DSC-Kurven weisen viele Peaks auf und ergebenH-Werte, die größer als die durch isotherme Messungen erhaltenen sind. Diese Ergebnisse können erklärt werden, wenn die Säurekonzentration, die unterschiedliche Reaktivität der Wasserstoffatome der Phosphorsäure und die Möglichkeit des Verlaufs sekundärer Reaktionen in Rechnung gestellt werden.
() () . 11 12/3, H, –91.0 –100.5 ·–1. , , H . , , .相似文献