A method for producing bifunctional furan epoxy (BFFE) according to various embodiments of the present disclosure uses a bio-based monofunctional furan raw material to produce BFFE, and may include synthesizing BFFE raw material by reacting furfuryl alcohol, formaldehyde, and an acid-base mixture catalyst, and polymerizing BFFE by adding epichlorohydrin (ECH), a base catalyst, and a solvent to the BFFE raw material.

Draw compounds and draw solutions comprising said draw compounds for use in forward osmosis solvent purification systems. The draw compound may be a linear random, sequential, or block molecular chain consisting of at least one oxide monomer or diol monomer and have a temperature-dependent affinity with a feed solvent. The draw compound may further include a first terminal group and a second terminal group, at least one of the first terminal group and the second terminal group selected from the group consisting of a hydroxyl group, an amine group, a carboxylic group, an allyl group, and a C1 to C14 substituted and unsubstituted alkyl group. The draw compound may also be a branched random, sequential, or block molecular chain consisting of at least one oxide monomer or diol monomer.

A process can be used for preparing polyether-modified polybutadienes. The process involves reacting at least one polybutadiene (A) with at least one epoxidizing reagent (B) to give at least one epoxy-functional polybutadiene (C). The at least one epoxy-functional polybutadiene (C) is then reacted with at least one hydroxy-functional compound (D) to give at least one hydroxy-functional polybutadiene (E). The at least one hydroxy-functional polybutadiene (E) is finally reacted with at least one epoxy-functional compound (F) to give at least one polyether-modified polybutadiene (G).

A surfactant comprising the reaction product of: (a) an epoxidised carboxylic acid ester; and (b) a compound including at least one reactive alcohol and/or amino functional group.

Provided is a resin composition from which a three-dimensional molding can be produced at an appropriate speed and with high dimensional accuracy, wherein the obtained three-dimensional molding has high strength. This resin composition is used in a method for producing a three-dimensional molding composed of a cured product of a liquid resin composition by selectively irradiating the liquid resin composition with active energy rays. The resin composition includes at least: a first polymerizable compound, in a liquid state at room temperature, having radical polymerizability; a second polymerizable compound, in a liquid state at room temperature, having no radical polymerizability; and a filler, wherein the surface of the filler is covered with the second polymerizable compound.

Provided is a resin composition from which a three-dimensional molding can be produced at an appropriate speed and with high dimensional accuracy, wherein the obtained three-dimensional molding has high strength. This resin composition is used in a method for producing a three-dimensional molding composed of a cured product of a liquid resin composition by selectively irradiating the liquid resin composition with active energy rays. The resin composition includes at least: a first polymerizable compound, in a liquid state at room temperature, having radical polymerizability; a second polymerizable compound, in a liquid state at room temperature, having no radical polymerizability; and a filler, wherein the surface of the filler is covered with the second polymerizable compound.

Draw compounds and draw solutions comprising said draw compounds for use in forward osmosis solvent purification systems. The draw compound may be a linear random, sequential, or block molecular chain consisting of at least one oxide monomer or diol monomer and have a temperature-dependent affinity with a feed solvent. The draw compound may further include a first terminal group and a second terminal group, at least one of the first terminal group and the second terminal group selected from the group consisting of a hydroxyl group, an amine group, a carboxylic group, an allyl group, and a C1 to C14 substituted and unsubstituted alky group. The draw compound may also be a branched random, sequential, or block molecular chain consisting of at least one oxide monomer or diol monomer.

Draw compounds and draw solutions comprising said draw compounds for use in forward osmosis solvent purification systems. The draw compound may be a linear random, sequential, or block molecular chain consisting of at least one oxide monomer or diol monomer and have a temperature-dependent affinity with a feed solvent. The draw compound may further include a first terminal group and a second terminal group, at least one of the first terminal group and the second terminal group selected from the group consisting of a hydroxyl group, an amine group, a carboxylic group, an allyl group, and a C1 to C14 substituted and unsubstituted alky group. The draw compound may also be a branched random, sequential, or block molecular chain consisting of at least one oxide monomer or diol monomer.

A solid polymer electrolyte precursor composition includes (i) one or more organic solvents; (ii) one or more cellulosic polymers dissolved in the organic solvent(s); (iii) one or more polymerizable components dissolved or dispersed in the organic solvent(s); (iv) one or more photo-initiators dissolved or dispersed in the organic solvent(s), where at least one of the one or more photo-initiators, following irradiation with light, promotes polymerization of at least one of the one or more polymerizable components; (v) one or more lithium ion sources dissolved or dispersed in the organic solvent(s); (vi) one or more plasticizers dissolved or dispersed in the organic solvent(s); and (vii) one or more ceramic particles dissolved or dispersed in the organic solvent(s).

A solid polymer electrolyte precursor composition includes (i) one or more organic solvents; (ii) one or more cellulosic polymers dissolved in the organic solvent(s); (iii) one or more polymerizable components dissolved or dispersed in the organic solvent(s); (iv) one or more photo-initiators dissolved or dispersed in the organic solvent(s), where at least one of the one or more photo-initiators, following irradiation with light, promotes polymerization of at least one of the one or more polymerizable components; (v) one or more lithium ion sources dissolved or dispersed in the organic solvent(s); (vi) one or more plasticizers dissolved or dispersed in the organic solvent(s); and (vii) one or more ceramic particles dissolved or dispersed in the organic solvent(s).