Provided is a method for decomposing a plastic composite with which it is possible to sufficiently decompose the matrix resins of the plastic composite in a short time even when the heating temperature of the plastic composite is low. In this method for decomposing a plastic composite, the plastic composite is brought into contact with an inorganic oxide catalyst having a band gap of 4 eV or less in a reactor, and the atmospheric temperature in the reactor is set at 380 to 530° C. in the presence of oxygen, and the surface temperature of the plastic composite is 480 to 650° C., which is at least 50° C. higher than the atmospheric temperature.

According to this invention, a Ni—Mo—W trimetallic catalyst supported on porous alumina is obtained that shows very high activity for hydrotreating (HDT) of gasoils, particularly deep hydrodesulfurization (HDS) and hydrodesnitrogenation (HDN) of straight run gasoil in conditions of moderate pressure. When the catalyst is applied to HDT of diesel, the NiMoW catalyst exhibits high catalytic activity. The content of sulfur and nitrogen in the resulting diesel can be reduced from 13,200 to 10 ppm and nitrogen from 360 ppm to less than 1 ppm, under moderate pressure, temperature and space-velocity (LHSV) similar to those of an industrial unit. The catalytic composition, of trimetallic type, is prepared from an alumina support of high surface area to which a solution containing a metal precursor of an element of group VIB is added, followed by other solution that contains one of the precursors of the active metallic phase, a solution containing another of the precursors of the active metallic phase from group VIB, a metal promoter of group VIII and an additive promoter of acidity from group VB, and finally another solution containing a metal of group VIB, a metal of Group VIII and an organic compound, the used route promotes the preferential formation of well dispersed structures of the used metals on the support of porous alumina, less refractory to sulfidation, with high stacking and short lengths of metal sulfides formed in the resulting hydrodesulfurization catalyst. In the formulation, at least a percentage, but not all the Mo is replaced by W, in a Mo/W molar ratio of 0.6 to 2.0.

According to this invention, a Ni—Mo—W trimetallic catalyst supported on porous alumina is obtained that shows very high activity for hydrotreating (HDT) of gasoils, particularly deep hydrodesulfurization (HDS) and hydrodesnitrogenation (HDN) of straight run gasoil in conditions of moderate pressure. When the catalyst is applied to HDT of diesel, the NiMoW catalyst exhibits high catalytic activity. The content of sulfur and nitrogen in the resulting diesel can be reduced from 13,200 to 10 ppm and nitrogen from 360 ppm to less than 1 ppm, under moderate pressure, temperature and space-velocity (LHSV) similar to those of an industrial unit. The catalytic composition, of trimetallic type, is prepared from an alumina support of high surface area to which a solution containing a metal precursor of an element of group VIB is added, followed by other solution that contains one of the precursors of the active metallic phase, a solution containing another of the precursors of the active metallic phase from group VIB, a metal promoter of group VIII and an additive promoter of acidity from group VB, and finally another solution containing a metal of group VIB, a metal of Group VIII and an organic compound, the used route promotes the preferential formation of well dispersed structures of the used metals on the support of porous alumina, less refractory to sulfidation, with high stacking and short lengths of metal sulfides formed in the resulting hydrodesulfurization catalyst. In the formulation, at least a percentage, but not all the Mo is replaced by W, in a Mo/W molar ratio of 0.6 to 2.0.

A catalyst system has been designed that disrupts the sedimentation process. The catalyst system achieves this by saturating key feed components before the feed components are stripped into their incompatible aromatic cores. The efficacy of this disruptive catalyst system is particularly evident in a hydrocracker configuration that runs in two-stage-recycle operation. The catalyst is a self-supported multi-metallic catalyst prepared from a precursor in the hydroxide form, and the catalyst must be toward the top level of the second stage of the two-stage system.

A catalyst system has been designed that disrupts the sedimentation process. The catalyst system achieves this by saturating key feed components before the feed components are stripped into their incompatible aromatic cores. The efficacy of this disruptive catalyst system is particularly evident in a hydrocracker configuration that runs in two-stage-recycle operation. The catalyst is a self-supported multi-metallic catalyst prepared from a precursor in the hydroxide form, and the catalyst must be toward the top level of the second stage of the two-stage system.

The present disclosure belongs to the technical field of catalysis, and particularly relates to a metal oxide coated ceramic corrugated plate catalyst, its preparation method and application thereof in preparation of key intermediates of citral. The catalyst consists of a ceramic corrugated plate carrier and a metal oxide active layer coated on a surface of the carrier, wherein the metal oxide active layer is a metal oxide formed by active ingredient titanium and at least four other metal elements selected from vanadium, chromium, manganese, iron, zirconium, niobium and molybdenum.

The present disclosure belongs to the technical field of catalysis, and particularly relates to a metal oxide coated ceramic corrugated plate catalyst, its preparation method and application thereof in preparation of key intermediates of citral. The catalyst consists of a ceramic corrugated plate carrier and a metal oxide active layer coated on a surface of the carrier, wherein the metal oxide active layer is a metal oxide formed by active ingredient titanium and at least four other metal elements selected from vanadium, chromium, manganese, iron, zirconium, niobium and molybdenum.

Provided is a method for preparing a diol. In the method, a saccharide and hydrogen as raw materials are contacted with a catalyst in water to prepare the diol. The employed catalyst is a composite catalyst comprised of a main catalyst and a cocatalyst, wherein the main catalyst is a water-insoluble acid-resistant alloy; and the cocatalyst is a soluble tungstate and/or soluble tungsten compound. The method uses an acid-resistant, inexpensive and stable alloy needless of a support as a main catalyst, and can guarantee a high yield of the diol in the case where the production cost is relatively low.

Provided is a method for preparing a diol. In the method, a saccharide and hydrogen as raw materials are contacted with a catalyst in water to prepare the diol. The employed catalyst is a composite catalyst comprised of a main catalyst and a cocatalyst, wherein the main catalyst is a water-insoluble acid-resistant alloy; and the cocatalyst is a soluble tungstate and/or soluble tungsten compound. The method uses an acid-resistant, inexpensive and stable alloy needless of a support as a main catalyst, and can guarantee a high yield of the diol in the case where the production cost is relatively low.

Oxidative dehydrogenation catalysts for converting lower paraffins to alkenes such as ethane to ethylene when prepared as an agglomeration, for example extruded with supports comprising slurries of Nb.sub.2O.sub.5.