Patent classifications
B01J23/26
Olefin production method using circulating fluidized bed process
Disclosed is an olefin production method which includes: (a) providing the regenerated catalyst and the hydrocarbon including not less than 90 wt % of LPG into Riser of Fast Fluidization Regime, and dehydrogenating in the presence of an alumina type catalyst; (b) separating an effluent from the dehydrogenation reaction into the catalyst and propylene mixture; (c) stripping to remove the hydrocarbon compound included in the catalyst separated at stage (b); (d) mixing the catalyst stripped at stage (c) with the gas including oxygen, and continuously regenerating it; (e) recycling the catalyst regenerated at stage (d) to stage (a), and providing it again into Riser; and (f) producing propylene product by cooling, compressing and separating propylene mixture of the reaction product separated at stage (b).
PROCESS FOR THE PREPARATION OF 1,1,1,2,2-PENTAFLUOROPROPANE
The present invention provides a process for preparing 1,1,1,2,2-pentafluoropropane (245cb), the process comprising gas phase catalytic dehydrochlorination of a composition comprising 1,1,1-trifluoro-2,3-dichloropropane (243db) to produce an intermediate composition comprising 3,3,3-trifluoro-2-chloro-prop-1-ene (CF.sub.3CCICH.sub.2, 1233xf), hydrogen chloride (HCl) and, optionally, air; and gas phase catalytic fluorination with hydrogen fluoride (HF) of the intermediate composition to produce a reactor product composition comprising 245c, HF, HCl and air; wherein the process is carried out with a co-feed of air.
PROCESS FOR THE PREPARATION OF 1,1,1,2,2-PENTAFLUOROPROPANE
The present invention provides a process for preparing 1,1,1,2,2-pentafluoropropane (245cb), the process comprising gas phase catalytic dehydrochlorination of a composition comprising 1,1,1-trifluoro-2,3-dichloropropane (243db) to produce an intermediate composition comprising 3,3,3-trifluoro-2-chloro-prop-1-ene (CF.sub.3CCICH.sub.2, 1233xf), hydrogen chloride (HCl) and, optionally, air; and gas phase catalytic fluorination with hydrogen fluoride (HF) of the intermediate composition to produce a reactor product composition comprising 245c, HF, HCl and air; wherein the process is carried out with a co-feed of air.
METAL HYDROXIDE BASED IONIC LIQUID COMPOSITION
The present disclosure relates to an ionic liquid composition and a process for its preparation. The process of the present disclosure is simple, single pot and efficient process for preparing the ionic liquid composition which is effective in a Friedel Craft reaction like, alkylation reaction, trans-alkylation, and acylation.
The present disclosure envisages an ionic liquid composition comprising at least one metal hydroxide; at least one metal halide; and at least one solvent. Also envisaged is a process for preparing an ionic liquid composition. The process comprises mixing in a reaction vessel, at least one metal hydroxide and at least one metal halide in the presence of at least one solvent under a nitrogen atmosphere and continuous stirring followed by cooling under continuous stirring to obtain the ionic liquid composition.
Methods for Improving Color Stability in Polyethylene Resins
Polymer compositions containing a titanated chromium-based ethylene polymer, 150-350 ppm of zinc stearate and/or calcium stearate, 50-5000 ppm of a phenolic antioxidant, 200-3000 ppm of a diphosphite antioxidant, and optionally, 200-3000 ppm of a monophosphite antioxidant, are described. These polymer compositions have improved long-term color stability, as well as lower levels of color formation after aging.
Methods for Improving Color Stability in Polyethylene Resins
Polymer compositions containing a titanated chromium-based ethylene polymer, 150-350 ppm of zinc stearate and/or calcium stearate, 50-5000 ppm of a phenolic antioxidant, 200-3000 ppm of a diphosphite antioxidant, and optionally, 200-3000 ppm of a monophosphite antioxidant, are described. These polymer compositions have improved long-term color stability, as well as lower levels of color formation after aging.
Methods for improving color stability in polyethylene resins
Polymer compositions containing a titanated chromium-based ethylene polymer, 150-350 ppm of zinc stearate and/or calcium stearate, 50-5000 ppm of a phenolic antioxidant, 200-3000 ppm of a diphosphite antioxidant, and optionally, 200-3000 ppm of a monophosphite antioxidant, are described. These polymer compositions have improved long-term color stability, as well as lower levels of color formation after aging.
Methods for improving color stability in polyethylene resins
Polymer compositions containing a titanated chromium-based ethylene polymer, 150-350 ppm of zinc stearate and/or calcium stearate, 50-5000 ppm of a phenolic antioxidant, 200-3000 ppm of a diphosphite antioxidant, and optionally, 200-3000 ppm of a monophosphite antioxidant, are described. These polymer compositions have improved long-term color stability, as well as lower levels of color formation after aging.
Oxygen-free direct conversion of methane and catalysts therefor
A process of methane catalytic conversion produces olefins, aromatics, and hydrogen under oxygen-free, continuous flowing conditions. Such a process has little coke deposition and realizes atom-economic conversion. Under the conditions encountered in a fixed bed reactor (i.e. reaction temperature: 750-1200 C.; reaction pressure: atmospheric pressure; the weight hourly space velocity of feed gas: 1000-30000 ml/g/h; and fixed bed), conversion of methane is 8-50%. The selectivity of olefins is 30-90%. And selectivity of aromatics is 10-70%. The catalyst for this methane conversion has a SiO.sub.2-based matrix having active species that are formed by confining dopant metal atoms in the lattice of the matrix.
Oxygen-free direct conversion of methane and catalysts therefor
A process of methane catalytic conversion produces olefins, aromatics, and hydrogen under oxygen-free, continuous flowing conditions. Such a process has little coke deposition and realizes atom-economic conversion. Under the conditions encountered in a fixed bed reactor (i.e. reaction temperature: 750-1200 C.; reaction pressure: atmospheric pressure; the weight hourly space velocity of feed gas: 1000-30000 ml/g/h; and fixed bed), conversion of methane is 8-50%. The selectivity of olefins is 30-90%. And selectivity of aromatics is 10-70%. The catalyst for this methane conversion has a SiO.sub.2-based matrix having active species that are formed by confining dopant metal atoms in the lattice of the matrix.