B01J31/0285

Ultrafast catalytic CO.SUB.2 .capture catalyzed by a novel ultrasound-treated ionic liquid

A transformational energy efficient technology using ionic liquid (IL) to couple with monoethanolamine (MEA) for catalytic CO.sub.2 capture is disclosed. [EMmim.sup.+][NTF.sub.2.sup.−] based catalysts are rationally synthesized and used for CO.sub.2 capture with MEA. A catalytic CO.sub.2 capture mechanism is disclosed according to experimental and computational studies on the [EMmim.sup.+][NTF.sub.2.sup.−] for the reversible CO.sub.2 sorption and desorption.

Electrocatalytic Process For Carbon Dioxide Conversion
20170259206 · 2017-09-14 ·

An electrocatalytic process for carbon dioxide conversion includes combining a Catalytically Active Element and a Helper Polymer in the presence of carbon dioxide, allowing a reaction to proceed to produce a reaction product, and applying electrical energy to said reaction to achieve electrochemical conversion of said carbon dioxide reactant to said reaction product. The Catalytically Active Element can be a metal in the form of supported or unsupported particles or flakes with an average size between 0.6 nm and 100 nm. The reaction products comprise at least one of CO, HCO.sup.−, H.sub.2CO, (HCO.sub.2).sup.−, H.sub.2CO.sub.2, CH.sub.3OH, CH.sub.4, C.sub.2H.sub.4, CH.sub.3CH.sub.2OH, CH.sub.3COO.sup.−, CH.sub.3COOH, C.sub.2H.sub.6, (COOH).sub.2, (COO.sup.−).sub.2, and CF.sub.3COOH.

ULTRAFAST CATALYTIC CO2 CAPTURE CATALYZED BY A NOVEL ULTRASOUND-TREATED IONIC LIQUID

A transformational energy efficient technology using ionic liquid (IL) to couple with monoethanolamine (MEA) for catalytic CO.sub.2 capture is disclosed. [EMmim.sup.+][NTF.sub.2.sup.−] based catalysts are rationally synthesized and used for CO.sub.2 capture with MEA. A catalytic CO.sub.2 capture mechanism is disclosed according to experimental and computational studies on the [EMmim.sup.+][NTF.sub.2.sup.−] for the reversible CO.sub.2 sorption and desorption.

METHOD CAPABLE OF REALIZING PREPARATION AND IN-SITU SEPARATION OF OLIGOMERIC RICINOLEATE

The disclosure is about a method capable of realizing the preparation and in-situ separation of the oligomeric ricinoleate, which uses the ricinoleic acid as raw material, and uses a protonic acid-type ionic liquid as a catalyst to cause the dehydration and esterification reactions between ricinoleic acid molecules. By continuously distilling out the generated water under a reduced pressure, the oligomeric ricinoleate with a polymerization degree of 2 to 10 is obtained. After the reaction, a method of washing with water or static stratification is selected to recover the catalyst according to the miscibility of the catalyst and reaction system. In his disclosure, renewable raw materials are used, the process is clean and pollution-free, and the operation is simple.

Catalyst bound alpha radical and synthesis of OXO compounds using the same

The present invention discloses in situ generated catalyst bound alpha radical compound represented by formula (I) or (II) and a single pot process for the preparation of oxo compounds by using in situ generated catalyst bound alpha radical compound of formula (I) or (II).

OXYGEN GENERATOR AND METHOD OF DECELERATING OR STOPPING THE OXYGEN PRODUCTION OF AN OXYGEN GENERATING COMPOSITION
20210253423 · 2021-08-19 ·

An oxygen generator uses a composition for generating oxygen and an acidic compound, with the composition for generating oxygen including an oxygen source, an ionic liquid, a metal oxide compound and optionally a basic compound. The oxygen source is a peroxide compound, the ionic liquid is in the liquid state at least in a temperature range from −10° C. to +50° C., the metal oxide compound is an oxide of a single metal or of two or more different metals which are from groups 2 to 14 of the periodic table of the elements. There is also described a method for decelerating or stopping the oxygen production from an oxygen generating composition, and a device for generating oxygen in a controlled manner.

A CATALYST BOUND ALPHA RADICAL AND SYNTHESIS OF OXO COMPOUNDS USING THE SAME
20210147364 · 2021-05-20 ·

The present invention discloses in situ generated catalyst bound alpha radical compound represented by formula (I) or (II) and a single pot process for the preparation of oxo compounds by using in situ generated catalyst bound alpha radical compound of formula (I) or (II).

OXYGEN GENERATOR AND METHOD FOR STARTING OR ACCELERATING THE OXYGEN PRODUCTION OF AN OXYGEN GENERATING COMPOSITION
20210147232 · 2021-05-20 ·

An oxygen generator has a composition for generating oxygen and a basic compound. The composition for generating oxygen includes an oxygen source, an ionic liquid, a metal salt, and an optional basic compound. The oxygen source is a peroxide compound, the ionic liquid is in the liquid state at least in a temperature range from −10° C. to +50° C., the metal salt has one single metal or two or more different metals, and an organic and/or an inorganic anion. There is also described a method for starting or accelerating the oxygen production of an oxygen generating composition, and a device for generating oxygen in a controlled manner.

Oxygen generator and method of controlling the oxygen production rate of an oxygen generator

An oxygen generator has a composition for generating oxygen and an acidic compound and/or a basic compound. The composition for generating oxygen includes an oxygen source, an ionic liquid, a metal oxide compound and/or a metal salt, and optionally a basic compound. The oxygen source is a peroxide compound, the ionic liquid is in the liquid state at least in a temperature range from 10 C. to +50 C., the metal oxide compound is an oxide of a single metal or of two or more different metals selected from the metals of groups 2 to 14 of the periodic table of the elements. The metal salt has a single metal or two or more different metals, and an organic and/or an inorganic anion. There is also described a method for controlling the oxygen production rate of the oxygen generator, and a device for generating oxygen in a controlled manner.

Method for preparing maleate by selective catalytic oxidation of lignin

The invention discloses a method for preparing maleate by selective catalytic oxidation of lignin. The method uses a heteropolyacid functionalized ionic liquid as a catalyst, and an aqueous alcohol solution as a reaction medium to achieve high-efficiency selective catalytic conversion and ring opening oxidation of biomass lignin at a reaction temperature of 110-160 C. and an oxygen pressure of 0.5-1.0 MPa for 1-6 h. The selectivity of maleate is higher than 47.83%. The yield and selectivity of a single chemical derived from the depolymerization of lignin in the present invention are much higher than the prior art, and the ionic liquid catalyst exhibits outstanding advantages such as availability of recovery and recycling through simple temperature adjustment; the reaction conditions of the present invention are mild, and the process is green and safe, easy to operate, and available for batch and continuous production. The invention provides a new green way for preparing bulk chemicals like maleate from reproducible raw materials such as lignin.