C07C1/2076

Method for producing methacrylic acid ester

Production of methacrylic acid ester comprising a step of having acetone undergo a dehydration reaction in the presence of a dehydration reaction catalyst to obtain a reaction mixture; a step of separating a mixture containing propyne and propadiene as main components from the obtained reaction mixture; a step of separating the separated mixture containing propyne and propadiene as main components into a liquid, gas, or gas-liquid mixture containing propyne as a main component, and a liquid, gas, or gas-liquid mixture containing propadiene as a main component; and a step of bringing the obtained liquid, gas, or gas-liquid mixture containing propyne as a main component into contact with carbon monoxide and an alcohol having 1 to 3 carbon atoms in the presence of a catalyst containing at least one selected from the group consisting of Group 8 metal elements, Group 9 metal elements, and Group 10 metal elements.

Preparation of pentanol with ethanol derived from fermentation

In one embodiment, the present application discloses methods to selectively synthesize higher alcohols and hydrocarbons useful as fuels and industrial chemicals from syngas and biomass. Ketene and ketonization chemistry along with hydrogenation reactions are used to synthesize fuels and chemicals. In another embodiment, ketene used to form fuels and chemicals may be manufactured from acetic acid which in turn can be synthesized from synthesis gas which is produced from coal, biomass, natural gas, etc.

Synthesis of high caloric fuels and chemicals via ketene and diketene intermediates

In one embodiment, the present application discloses methods to selectively synthesize higher alcohols and hydrocarbons useful as fuels and industrial chemicals from syngas and biomass. Ketene and ketonization chemistry along with hydrogenation reactions are used to synthesize fuels and chemicals. In another embodiment, ketene used to form fuels and chemicals may be manufactured from acetic acid which in turn can be synthesized from synthesis gas which is produced from coal, biomass, natural gas, etc.

Method and system embodiments for converting ethanol to para-xylene and ortho-xylene

Disclosed herein are embodiments of a method and system for converting ethanol to para-xylene. The method also provides a pathway to produce terephthalic acid from biomass-based feedstocks. In some embodiments, the disclosed method produces p-xylene with high selectivity over other aromatics typically produced in the conversion of ethanol to xylenes, such as m-xylene, ethyl benzene, benzene, toluene, and the like. And, in some embodiments, the method facilitates the ability to use ortho/para mixtures of methylbenzyaldehyde for preparing ortho/para xylene product mixtures that are amendable to fractionation to separate the para- and ortho-xylene products thereby providing a pure feedstock of para-xylene that can be used to form terephthalic anhydride and a pure feedstock of ortho-xylene that can be used for other purposes, such as phthalic anhydride.

Preparation method and production device for propylene

A process for producing propylene involves dehydration of isopropanol. The dehydration process includes a step of subjecting a starting material containing isopropanol to a dehydration reaction in the presence of a dehydration catalyst comprising alumina to produce a product containing propylene. The starting material has a water content of 0.1 to 10.0 wt % (relative to 100 wt % of the total mass of the starting material), and the product has a total content of C2 unsaturated impurities and C3-C4 unsaturated impurities of 80 ppm or less (relative to 100 wt % of the total mass of the product).

Process for producing diesel fuel and aviation fuel from renewable feedstocks having improving yields
09567264 · 2017-02-14 · ·

A process for producing aviation fuel and diesel from renewable feedstock is described. This process involves introducing the renewable feedstock into a hydrogenation and deoxygenation zone, and separating the hydrocarbon effluent from the hydrogenation and deoxygenation zone into an aviation boiling range fraction and a diesel boiling range fraction. The aviation boiling range fraction and diesel boiling range fraction are alternately sent to the isomerization and selective hydrocracking zone. This allows for lower severity isomerization and selective hydrocracking zone operating conditions when processing oils that naturally contain medium and long carbon chains (C.sub.8-C.sub.18), such as coconut or palm kernel oil. The lower severity operation results in decreased cracking, increasing the yield of aviation fuel product.

CONVERSION OF OLIGOMERIC STARCH, CELLULOSE, HYDROLYSATES OR SUGARS TO HYDROCARBONS

Embodiments of the present invention are directed to the conversion of a source material (e.g., a depolymerized oligosaccharide mixture, a monomeric sugar, a hydrolysate, or a mixture of monomeric sugars) to intermediate molecules containing 7 to 26 contiguous carbon atoms. These intermediates may also be converted to saturated hydrocarbons. Such saturated hydrocarbons are useful as, for example, fuels.

BUTADIENE PRODUCTION FROM USED TIRES
20250257187 · 2025-08-14 ·

A process comprising (a) providing a feedstock that includes carbonaceous materials; (b) gasifying the feedstock to produce a gaseous stream including carbon monoxide, hydrogen, and carbon dioxide; (c) converting at least a portion of the carbon monoxide, hydrogen, and carbon dioxide to ethanol; and (d) converting at least a portion of the ethanol to butadiene monomer.

CATALYST FOR THE PRODUCTION OF 1,3-BUTADIENE COMPRISING AN ALUMINIUM-CONTAINING SUPPORT WITH HIGH FAVORABLE WEIGHT HOURLY SPACE VELOCITY

The present invention relates to a supported catalyst comprising a support and 0.1 to 10 wt. % of tantalum, calculated as Ta.sub.2O.sub.5 and based on the total weight of the catalyst, wherein the supported catalyst further comprises from 50 to 350 ppm of aluminium and from 1 to 50 ppm of sodium, based on the total weight of the catalyst, respectively. Moreover, the invention relates to a catalyst reaction tube for the production of 1,3-butadiene comprising at least one packing of the supported catalyst as defined herein, to a reactor for the production of 1,3-butadiene comprising one or more of the catalyst reaction tubes as defined herein, and to a plant for the production of 1,3-butadiene comprising one or more of the reactors as defined herein. The invention also relates to a process for the production of 1,3-butadiene as defined herein and to a process for the production of the supported catalyst as defined herein. Finally, the present invention relates to the use of the supported catalyst as defined herein for the production of 1,3-butadiene from a feed comprising ethanol and acetaldehyde and to the use of aluminium in an amount in a range of from 50 to 350 ppm in a supported catalyst for the production of 1,3-butadiene from a feed comprising ethanol and acetaldehyde for increasing the 1,3-butadiene productivity of the catalyst.

Process for the dehydrogenation of ethanol in a multitubular reactor

The invention relates to a process for the dehydrogenation of a feedstock comprising ethanol, using at least one multitubular reactor advantageously comprising a plurality of tubes comprising at least one dehydrogenation catalyst, and a calender, said feedstock being introduced into the tubes in gas form, at an inlet temperature of greater than or equal to 240 C., a pressure between 0.1 and 1.0 MPa, and a WWH between 2 and 15 h.sup.1, wherein a heat-transfer fluid circulates in said calender at a flow rate such that the weight ratio of said heat-transfer fluid relative to said feedstock is greater than or equal to 1.0, and such that said heat-transfer fluid is introduced into said calender in gas form at an inlet temperature of greater than or equal to 260 C. and at an inlet pressure of greater than or equal to 0.10 MPa, and less than or equal to 1.10 MPa, and leaves the calender at least partly in liquid form.