Patent classifications
C07C31/205
PROCESS FOR THE DIRECT CONVERSION OF CELLULOSE TO GLYCOLS USING NON-NOBLE METAL LOADED ZEOLITE CATALYSTS
The present invention relates to a process for the direct conversion of cellulose into glycols by using a non noble metal supported zeolite catalyst selected from Al—Ni—W/HY, Al—Ni—W/NaY and Al—Ni—W/Na-ZSM-5, wherein the ratio of the metal in the catalyst is in the range of 15%-12%-30% to 0%-3%-5%.
PROCESS FOR THE DIRECT CONVERSION OF CELLULOSE TO GLYCOLS USING NON-NOBLE METAL LOADED ZEOLITE CATALYSTS
The present invention relates to a process for the direct conversion of cellulose into glycols by using a non noble metal supported zeolite catalyst selected from Al—Ni—W/HY, Al—Ni—W/NaY and Al—Ni—W/Na-ZSM-5, wherein the ratio of the metal in the catalyst is in the range of 15%-12%-30% to 0%-3%-5%.
COMPOSITE CATALYST AND USE THEREOF IN PREPARING PROPYLENE GLYCOL
The present application provides a composite catalyst and use thereof in preparing propylene glycol, where the composite catalyst includes: a main catalyst; and an assistant catalyst, forming on the main catalyst; the assistant catalyst is a magnesium hydroxide shell with a cage-like shape forming on the surface of the main catalyst, and the main catalyst is located inside the magnesium hydroxide shell.
COMPOSITE CATALYST AND USE THEREOF IN PREPARING PROPYLENE GLYCOL
The present application provides a composite catalyst and use thereof in preparing propylene glycol, where the composite catalyst includes: a main catalyst; and an assistant catalyst, forming on the main catalyst; the assistant catalyst is a magnesium hydroxide shell with a cage-like shape forming on the surface of the main catalyst, and the main catalyst is located inside the magnesium hydroxide shell.
Methods for preparing diol
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.
Methods for preparing diol
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.
Method for Refining Bio-Based Propylene Glycol
The invention provides a process for refining bio-based propylene glycol, wherein impurities having boiling points close to that of propylene glycol are separated. In this process, C.sub.5-C.sub.20 oleophilic alcohol compounds, C.sub.5-C.sub.20 alkanes and/or C.sub.4-C.sub.20 oleophilic ketone compounds are subjected to azeotropism as an azeotropic solvent together with the bio-based propylene glycol to obtain an azeotrope containing propylene glycol. Then the azeotropic solvent in the azeotrope is separated to obtain a crude propylene glycol which is further purified to obtain propylene glycol.
Method for Refining Bio-Based Propylene Glycol
The invention provides a process for refining bio-based propylene glycol, wherein impurities having boiling points close to that of propylene glycol are separated. In this process, C.sub.5-C.sub.20 oleophilic alcohol compounds, C.sub.5-C.sub.20 alkanes and/or C.sub.4-C.sub.20 oleophilic ketone compounds are subjected to azeotropism as an azeotropic solvent together with the bio-based propylene glycol to obtain an azeotrope containing propylene glycol. Then the azeotropic solvent in the azeotrope is separated to obtain a crude propylene glycol which is further purified to obtain propylene glycol.
Oxidizing liquid media for chemical transformations
Provided is an oxidizing composition, in which a liquid medium is substantially inert in the presence of an oxidizing electrophile contained in the liquid medium. The composition comprises (a) an oxidizing electrophile comprising a main group element in oxidized form and at least one conjugate anion of an oxygen acid; (b) a non-oxidizable liquid selected from a fluorinated hydrocarbon, a sulfone, a deactivated arene, a deactivated aliphatic, a deactivated heteroarene, a deactivated heteroaliphatic, and a combination thereof; and (c) optionally one or more salt additives. Further provided are a method of using the oxidizing composition to oxidize a substrate and a method of generating and/or regenerating an oxidizing electrophile comprising a main group element.
PRE-TREATMENT OF LIGNOCELLULOSIC FEEDS FOR THE PRODUCTION OF GLYCOLS
A process for the preparing glycols from a lignocellulosic solid biomass involves contacting the biomass with an organic solvent comprising a low boiling point alcohol and a pre-treatment acid at a temperature in a range from 80 to 220° C. and a pressure in a range from 1 to 50 bara. The resulting mixture, having >20 wt. % water, is separated into a pre-treated solid residue comprising cellulose and a liquid stream comprising dissolved lignin and hemicellulose. The pre-treated solid residue is subjected to a hydrogenolysis reaction, generating a glycols stream, a lights stream, comprising a first portion of organic solvent, and a heavies stream. At least of part of the liquid stream is separated to produce a second portion of organic solvent and a solid residue of lignin and hemicellulose. At least part of the first and second portion of organic solvent is recycled to the contacting step.