Abstract: Oxidative dehydrogenation catalysts comprising MoVNbTeO having improved consistency of composition and a 25% conversion of ethylene at less than 420° C. and a selectivity to ethylene above 95% are prepared by treating the catalyst precursor with H2O2 in an amount equivalent to 0.30-2.8 mL H2O2 of a 30% solution per gram of catalyst precursor prior to calcining.

Abstract: In the operation of an oxidative dehydrogenation (ODH) process, it is desirable to remove oxygen in the product stream for a number of reasons, including to reduce oxidation of the product. This may be achieved by having several pre-reactors upstream of the main reactor having a catalyst system containing labile oxygen. The feed passes through one or more reactors saturated with labile oxygen. When the labile oxygen is consumed through a valve system, the pre-reactor accepts product from the main reactor and complexes reactive oxygen in the product stream until the catalyst system is saturated with labile oxygen. Then the reactor becomes a pre-reactor and another pre-reactor becomes a scavenger.

Abstract: Oxidative dehydrogenation of paraffins to olefins provides a lower energy route to produce olefins. Oxidative dehydrogenation processes may be integrated with a number of processes in a chemical plant such as polymerization processes, manufacture of glycols, and carboxylic acids and esters. Additionally, oxidative dehydrogenation processes can be integrated with the back end separation process of a conventional steam cracker to increase capacity at reduced cost.

Abstract: In the operation of an oxidative dehydrogenation (ODH) process, it is desirable to remove oxygen in the product stream for a number of reasons, including to reduce oxidation of the product. This may be achieved by having several pre-reactors upstream of the main reactor having a catalyst system containing labile oxygen. The feed passes through one or more reactors saturated with labile oxygen. When the labile oxygen is consumed through a valve system, the pre-reactor accepts product from the main reactor and complexes reactive oxygen in the product stream until the catalyst system is saturated with labile oxygen. Then the reactor becomes a pre-reactor and another pre-reactor becomes a scavenger.

Abstract: The present invention provides a process for the manufacture of an efficient and robust catalyst for the oxidative dehydrogenation of paraffins to olefins, preferably lower C2-4 paraffins. The present invention provides a process for the preparation of an oxidative dehydrogenation catalyst of C2-4 paraffins to olefins comprising comminuting: from 10 to 99 weight % of a mixed oxide catalyst of the formula VxMoyNbzTemMenOp, wherein Me is a metal selected from the group consisting of Ta, Ti, W, Hf, Zr, Sb and mixtures thereof; with from 90 to 1 weight % of an inert matrix selected from oxides of titanium, zirconia, aluminum, magnesium, yttria, lantana, silica and their mixed compositions or a carbon matrix to produce particles having a size from 1 to 100 microns and forming the resulting particles into pellets having a size from 0.1 to 2 mm.

Abstract: Oxidative dehydrogenation of paraffins to olefins provides a lower energy route to produce olefins. Oxidative dehydrogenation processes may be integrated with a number of processes in a chemical plant such as polymerization processes, manufacture of glycols, and carboxylic acids and esters. Additionally, oxidative dehydrogenation processes can be integrated with the back end separation process of a conventional steam cracker to increase capacity at reduced cost.

Abstract: The present invention provides a continuous process for the oxidative dehydrogenation of ethane to ethylene using a mixed oxide catalyst supported onto a ceramic membrane by supplying an oxygen containing gas (air or pure oxygen) and pure ethane to the opposite sides of the membrane, so that the paraffin and the oxygen do not directly mix in the reactor.

Abstract: The present invention provides a continuous process for the oxidative dehydrogenation of ethane to ethylene using a mixed oxide catalyst supported onto a ceramic membrane by supplying an oxygen containing gas (air or pure oxygen) and pure ethane to the opposite sides of the membrane, so that the paraffin and the oxygen do not directly mix in the reactor.

Abstract: The present invention provides a process for the manufacture of an efficient and robust catalyst for the oxidative dehydrogenation of paraffins to olefins, preferably lower C2-4 paraffins. The present invention provides a process for the preparation of an oxidative dehydrogenation catalyst of C2-4 paraffins to olefins comprising comminuting: from 10 to 99 weight % of a mixed oxide catalyst of the formula VxMoyNbzTemMenOp, wherein Me is a metal selected from the group consisting of Ta, Ti, W, Hf, Zr, Sb and mixtures thereof; with from 90 to 1 weight % of an inert matrix selected from oxides of titanium, zirconia, aluminum, magnesium, yttria, lantana, silica and their mixed compositions or a carbon matrix to produce particles having a size from 1 to 100 microns and forming the resulting particles into pellets having a size from 0.1 to 2 mm.

Abstract: The present invention provides a continuous process for the oxidative dehydrogenation of a lower paraffin to a lower olefin, preferably alpha olefin by sequentially providing pulses of an oxygen containing gas, an inert gas, the paraffin, and inert gas in the presence of a catalyst that preferably has the ability to hold and release oxygen, so that the paraffin and the oxygen do not directly mix in the reactor.

Abstract: The present invention provides a process for the oxidative dehydrogenation of a paraffin such as ethane to the corresponding alkene such as ethylene in which the alkane is contacted with a bed of oxidative dehydrogenation catalyst having an enhanced labile oxygen content in the crystal structure on an inert support optionally with a regenerable metallic oxidant composition in the absence of a gaseous feed containing oxygen.

Abstract: A process for the conversion of paraffin hydrocarbon feed stock via skeletal isomerisation by contacting this feed with a catalyst comprised of an ionic liquid formed from an N-containing heterocyclic and/or N-containing aliphatic organic cation and an inorganic anion derived from metal halides.

Abstract: A method and a catalyst are described for selective oxidation of aromatic compounds (e.g., benzene and its derivatives) into hydroxylated aromatic compounds (e.g., corresponding phenols). For example, benzene can be converted into phenol with a yield of at least 30-40%, and a selectivity on the basis of benzene of at least 95-97%. The selectivity for this reaction based on N2O is at least 90-95%. Therefore, no substantial N2O decomposition or consumption for complete benzene oxidation to CO+CO2 or other side products occurs. Similar results are obtained with benzene derivatives (e.g., fluorobenzene, difluorobenzene, phenol), although the selectivity is somewhat lower in the case of derivatives (e.g., about 80-85% in the case of fluorosubstituted benzenes). A preferred catalyst for this process is a composition containing a high-silica pentasil-type zeolite (e.g, an HZSM-5 type zeolite) which contains no purposefully introduced additives such as transition or noble metals.

Abstract: The invention relates to the field of organic synthesis, more specifically to a method for the production of phenol and cresol by the direct selective oxidation of benzene and toluene with nitrous oxide in the presence of a heterogeneous catalyst. Commercial high-silica zeolites are first calcined at a temperature of 500-950° C. sufficient to dehydroxylate it. It is then modified by the addition of modifying agents—zinc ions or zinc oxide—by applying a zinc compound to it. The catalyst is then activated in air or an inert gas at 300-850° C. The mixture of benzene or toluene with the nitrous oxide is brought into contact with the modified catalyst at 225 to 500° C.

Abstract: The invention relates to the field of organic synthesis, more specifically to a method for the production of phenol and cresol by the direct selective oxidation of benzene and toluene with nitrous oxide in the presence of a heterogeneous catalyst. Commercial high-silica zeolites are first calcined at a temperature of 500-950° C. sufficient to dehydroxylate it. It is then modified by the addition of modifying agents—zinc ions or zinc oxide—by applying a zinc compound to it. The catalyst is then activated in air or an inert gas at 300-850° C. The mixture of benzene or toluene with the nitrous oxide is brought into contact with the modified catalyst at 225 to 500° C.

Abstract: A method and a catalyst are described for selective oxidation of aromatic compounds (e.g., benzene and its derivatives) into hydroxylated aromatic compounds (e.g., corresponding phenols). For example, benzene can be converted into phenol with a yield of at least 30-40%, and a selectivity on the basis of benzene of at least 95-97%. The selectivity for this reaction based on N2O is at least 90-95%. Therefore, no substantial N2O decomposition or consumption for complete benzene oxidation to CO+CO2 or other side products occurs. Similar results are obtained with benzene derivatives (e.g., fluorobenzene, difluorobenzene, phenol), although the selectivity is somewhat lower in the case of derivatives (e.g., about 80-85% in the case of fluorosubstituted benzenes). A preferred catalyst for this process is a composition containing a high-silica pentasil-type zeolite (e.g, an HZSM-5 type zeolite) which contains no purposefully introduced additives such as transition or noble metals.

Abstract: A method and a catalyst are described for selective oxidation of aromatic compounds (e.g., benzene and its derivatives) into hydroxylated aromatic compounds (e.g., corresponding phenols). For example, benzene can be converted into phenol with a yield of at least 30-40%, and a selectivity on the basis of benzene of at least 95-97%. The selectivity for this reaction based on N2O is at least 90-95%. Therefore, no substantial N2O decomposition or consumption for complete benzene oxidation to CO+CO2 or other side products occurs. Similar results are obtained with benzene derivatives (e.g., fluorobenzene, difluorobenzene, phenol), although the selectivity is somewhat lower in the case of derivatives (e.g., about 80-85% in the case of fluorosubstituted benzenes). A preferred catalyst for this process is a composition containing a high-silica pentasil-type zeolite (e.g., an HZSM-5 type zeolite) which contains no purposefully introduced additives such as transition or noble metals.