A method for producing at least one oxidation product selected from the group consisting of acrolein and acrylic acid is provided. This method can alleviate concerns about deterioration of a gas-phase oxidation catalyst and reaction runaway in a restart period after a shutdown, and can allow the reaction to proceed in a stable state. Using a fixed-bed reactor filled with a gas-phase oxidation catalyst, at least one source gas selected from the group consisting of propylene and acrolein is subjected to a gas-phase contact oxidation reaction while a heating medium is caused to contact with or circulate through the fixed-bed reactor and thereby to heat the fixed-bed reactor. The temperature of the heating medium when the load is maximum in the restart period after the shutdown is controlled to be lower than the temperature of the heating medium when the load is maximum in an initial start-up period.

The present invention provides a method for increasing the UV transmittance of ethylene glycol. The method uses an ethylene glycol solution and hydrogen as raw materials, and uses an alloy catalyst comprising nickel, one or more rare-earth elements, tin, and aluminum, the contents thereof in parts by weight being 10-90, 1-5, 1-60, and 5-9, respectively. The method of the present invention uses an inexpensive, stable-in-aqueous-phase, carrier-free alloy as a catalyst, and continuously adds hydrogen to reduce unsaturated impurities in ethylene glycol. In application of the method of the present invention in continuous industrial-scale production, the use of this type of alloy catalyst could be especially significant for the achievement of long-term system stability and control of production costs.

The present specification provides a ferrite catalyst, a method for preparing the same and a method for preparing butadiene using the same.

Methods and compositions related to a selective catalytic reduction catalyst comprising iron and vanadium, wherein the vanadium is present as (1) one or more vanadium oxides, and (2) metal vanadate of the form Fe.sub.xM.sub.yVO.sub.4 where x=0.2 to 1 and y=1x, and where M comprises one or more non-Fe metals when y>0.

An object of the present invention is to provide a catalyst with high selectivity for an ,-unsaturated aldehyde, an ,-unsaturated carboxylic acid, and the like. Problems are solved by a catalyst containing at least molybdenum and bismuth and having a B/A of 1.3 to 5 when a ratio of the amount of bismuth atoms to the amount of molybdenum atoms, calculated from ICP (inductively coupled plasma) atomic emission spectrometry is A, and a ratio of a peak area of bismuth atoms to a peak area of molybdenum atoms, measured by X-ray photoelectron spectrometry is B.

A catalytic composition useful for the conversion of an olefin selected from the group consisting of propylene, isobutylene or mixtures thereof, to acrylonitrile, methacrylonitrile, and mixtures thereof. The catalytic composition comprises a complex of metal oxides comprising bismuth, molybdenum, iron, cerium and other promoters, with a desirable composition.

A catalytic composition useful for the conversion of an olefin selected from the group consisting of propylene, isobutylene or mixtures thereof, to acrylonitrile, methacrylonitrile, and mixtures thereof. The catalytic composition comprises a complex of metal oxides comprising bismuth, molybdenum, iron, cerium and other promoters, with a desirable composition.

Catalysts for hydrodesulfurization (HDS), e.g., of fuel such DBT in a batch reactor, may include Ce-modified SBA CoMo-sulfided catalysts. The dispersion and catalytic activity of the active species (CoMoS.sub.2) may be influenced by the CeSi network in the support. The physico-chemical properties of such catalyststextural properties, crystallinity, metal oxide reducibility, and Mo phaseswere established, and BET surface area, X-ray diffraction (XRD), and Raman spectroscopy analysis showed up to 2.5 wt. % Ce incorporation into the Si-network in SBA-15. Up to 2.5 wt. % Ce loading on the SBA-15 support can provide large BET surface area and total pore volume. The metal oxide reducibility and MoS.sub.2 phase in the sulfided 2.5CeSCoMo catalyst indicate moderate metal-support interaction at 2.5Ce wt. %. Improved HDS activity was shown with Ce loading up to 2.5 wt. %, possibly due to Ce's facilitation of metal oxide reduction and dispersion of the MoS.sub.2 active phase via metal-support interaction.

The present invention relates to a supported catalyst that can be used to produce a carbon nanotube aggregate with high bulk density, a method for preparing the supported catalyst, a carbon nanotube aggregate produced using the supported catalyst, and a method for producing the carbon nanotube aggregate. According to the present invention, the bulk density of the carbon nanotube aggregate is easily controllable. Therefore, the carbon nanotube aggregate is suitable for use in various fields.

A photocatalytic member comprises a base and a photocatalytic layer fixed on the base. The photocatalytic layer comprises first photocatalyst particles being visible light responsive photocatalyst particles for hydrogen generation, second photocatalyst particles being visible light responsive photocatalyst particles for oxygen generation, and conductive particles which are provided between the first photocatalyst particle and the second photocatalyst particle, have Fermi level at a negative position relative to an electronic energy level at the upper end of the valence band of the first photocatalyst particle and at a positive position relative to an electronic energy level at the bottom end of the conduction band of the second photocatalyst particle, and are able to store an electron and a hole. In the photocatalytic layer, the conductive particles are located to be coupled to both the first photocatalyst particles and the second photocatalyst particles.