The electrochemical energy conversion system of the present disclosure includes an anode, a cathode, and an ion exchange membrane including a polymer having an aromatic polymer chain and an alkylated substrate including an alkyl chain, and at least one ionic group. The alkylated substrate is bound to at least one aromatic group in the polymer chain via Friedel-Crafts alkylation of the at least one aromatic group. The alkylation reaction utilizes a haloalkylated tertiary alcohol or a haloalkylated alkene as a precursor. In the presence of an acid catalyst, a carbocation is generated in the precursor which reacts with the aromatic rings of the polymer chain. The at least one ionic group is then replaced with a desired cationic or anionic group using a substitution reaction. The membranes exhibit advantageous stability achieved through a simplified and scalable reaction scheme.

An ion exchange membrane having a structure that an ion exchange resin is filled in spaces of a porous base film, the porous base film has a structure that at least two porous olefin resin layers are laminated with a bonding strength of 100 gf/cm or more to less than 700 gf/cm and a Gurley air permeance of 500 sec/100 ml or less in terms of a 100 μm thick film. In this ion exchange membrane, base film has high air permeability though it has a multi-layer structure that a plurality of porous resin films are bonded together, and therefore a rise in electric resistance caused by the lamination of the base sheets is effectively suppressed.

An ion exchange membrane having a structure that an ion exchange resin is filled in spaces of a porous base film, the porous base film has a structure that at least two porous olefin resin layers are laminated with a bonding strength of 100 gf/cm or more to less than 700 gf/cm and a Gurley air permeance of 500 sec/100 ml or less in terms of a 100 μm thick film. In this ion exchange membrane, base film has high air permeability though it has a multi-layer structure that a plurality of porous resin films are bonded together, and therefore a rise in electric resistance caused by the lamination of the base sheets is effectively suppressed.

To provide an ion exchange membrane for alkali chloride electrolysis which has high membrane strength and low membrane resistance, thereby capable of reducing the electrolysis voltage during alkali chloride electrolysis. In this ion exchange membrane (1) for alkali chloride electrolysis, a reinforcing material 20 formed by weaving reinforcing yarns 22 and sacrificial yarns 24 is disposed in a layer (S) 14, and layer (S) 14 has elution portions 28 formed by elution of at least portions of the sacrificial yarns 24. In a cross section perpendicular to reinforcing yarns of the warp, the average distance (d1) from the center of a reinforcing yarn 22 to the center of the adjacent reinforcing yarn 22, the total area (P) obtained by adding the cross-sectional area of an elution portion 28 and the cross-sectional area of a sacrificial yarn 24 remaining in the elution portion 28, the number (n) of elution portions between adjacent reinforcing yarns 22, and the ion exchange capacity of a layer (Sa) located on the most anode side in the layer (S) 14 during alkali chloride electrolysis, are controlled to be within specific ranges, respectively.

To provide an ion exchange membrane for alkali chloride electrolysis which has high membrane strength and low membrane resistance, thereby capable of reducing the electrolysis voltage during alkali chloride electrolysis. In this ion exchange membrane (1) for alkali chloride electrolysis, a reinforcing material 20 formed by weaving reinforcing yarns 22 and sacrificial yarns 24 is disposed in a layer (S) 14, and layer (S) 14 has elution portions 28 formed by elution of at least portions of the sacrificial yarns 24. In a cross section perpendicular to reinforcing yarns of the warp, the average distance (d1) from the center of a reinforcing yarn 22 to the center of the adjacent reinforcing yarn 22, the total area (P) obtained by adding the cross-sectional area of an elution portion 28 and the cross-sectional area of a sacrificial yarn 24 remaining in the elution portion 28, the number (n) of elution portions between adjacent reinforcing yarns 22, and the ion exchange capacity of a layer (Sa) located on the most anode side in the layer (S) 14 during alkali chloride electrolysis, are controlled to be within specific ranges, respectively.

This invention relates to a process for the recovery of cobalt ions and tungstic acid and/or its derivatives from aqueous solutions, such as in particular the spent catalytic waters deriving from processes for the oxidative cleavage of vegetable oils. In particular this invention relates to a process for the recovery of cobalt ions and tungstic acid and/or its derivatives which provides for the use of cation-exchange resins.

This invention relates to a process for the recovery of cobalt ions and tungstic acid and/or its derivatives from aqueous solutions, such as in particular the spent catalytic waters deriving from processes for the oxidative cleavage of vegetable oils. In particular this invention relates to a process for the recovery of cobalt ions and tungstic acid and/or its derivatives which provides for the use of cation-exchange resins.

Method for preparing methyl formate and coproducing dimethyl ether by reacting a formaldehyde and methanol raw material (molar ratio range of 1:4 to 1:0.05) in a First Reaction Region at ranges from 50° C. to 100° C. with Catalyst A resulting in post-reaction material separated into Constituent I. Reacting Constituent I in a Second Reaction Region at ranges from 50° C. to 200° C. and from 0.1 MPa to 10 MPa with Catalyst B resulting in post-reaction material, which is separated into methyl formate, dimethyl ether and Constituent II. At least 1% of dimethyl ether is product, and recycling the rest to the First Reaction Region. Constituent II is recycled to the Second Reaction Region. Each component is gaseous phase and/or liquid phase, independently. The method shows long catalyst life, mild reaction condition, high utilization ratio of raw materials, continuous production and large scale industrial application potential.

Method for preparing methyl formate and coproducing dimethyl ether by reacting a formaldehyde and methanol raw material (molar ratio range of 1:4 to 1:0.05) in a First Reaction Region at ranges from 50° C. to 100° C. with Catalyst A resulting in post-reaction material separated into Constituent I. Reacting Constituent I in a Second Reaction Region at ranges from 50° C. to 200° C. and from 0.1 MPa to 10 MPa with Catalyst B resulting in post-reaction material, which is separated into methyl formate, dimethyl ether and Constituent II. At least 1% of dimethyl ether is product, and recycling the rest to the First Reaction Region. Constituent II is recycled to the Second Reaction Region. Each component is gaseous phase and/or liquid phase, independently. The method shows long catalyst life, mild reaction condition, high utilization ratio of raw materials, continuous production and large scale industrial application potential.

This invention is in the field of micro-organism and algal cell processing. The invention relates to a method of maximizing migration of micro-organism and/or algal cells to a solvent fraction while simultaneously displacing water in a separate fraction and subsequent extraction of hydrophobic products from the organisms. The invention further relates to a method of sequestration of protein from an aqueous phase to an organic solvent.