A polymer, includes a first structural unit represented by formula (1), a second structural unit represented by formula (2-1), formula (2-2), or both, and a third structural unit represented by formula (3-1), formula (3-2), or both. The polymer preferably has a weight-average molecular weight in terms of polystyrene of 500 or more and 400,000 or less. A composition includes the polymer and an organic solvent. A molded body includes the polymer.

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A polymer, includes a first structural unit represented by formula (1), a second structural unit represented by formula (2-1), formula (2-2), or both, and a third structural unit represented by formula (3-1), formula (3-2), or both. The polymer preferably has a weight-average molecular weight in terms of polystyrene of 500 or more and 400,000 or less. A composition includes the polymer and an organic solvent. A molded body includes the polymer.

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An interfacial process for preparing a poly(aliphatic ester-carbonate) includes providing an initial polymerization reaction mixture comprising an aliphatic C6-20 dicarboxylic acid, a bisphenol, an alkali hydroxide, and optionally a catalyst in a solvent system comprising water and an immiscible organic solvent, adding an initial portion of a carbonyl dihalide over a first time period while maintaining the reaction at a first pH from 7 to 8; and adding a second portion of the carbonyl dihalide over a second, subsequent time period while maintaining the reaction pH at a second pH from 9 to 12, to provide a product polymerization mixture, wherein the amount of alkali hydroxide in the initial polymerization reaction mixture is effective to increase the fraction of the first time period at a measured pH of 7 to 8 compared to the same reaction mixture with a higher amount of alkali hydroxide in the initial polymerization mixture.

An interfacial process for preparing a poly(aliphatic ester-carbonate) includes providing an initial polymerization reaction mixture comprising an aliphatic C6-20 dicarboxylic acid, a bisphenol, an alkali hydroxide, and optionally a catalyst in a solvent system comprising water and an immiscible organic solvent, adding an initial portion of a carbonyl dihalide over a first time period while maintaining the reaction at a first pH from 7 to 8; and adding a second portion of the carbonyl dihalide over a second, subsequent time period while maintaining the reaction pH at a second pH from 9 to 12, to provide a product polymerization mixture, wherein the amount of alkali hydroxide in the initial polymerization reaction mixture is effective to increase the fraction of the first time period at a measured pH of 7 to 8 compared to the same reaction mixture with a higher amount of alkali hydroxide in the initial polymerization mixture.

A magnetic resonance system may include a magnetic resonance magnet and a storage container configured to accommodate the magnetic resonance magnet. The storage container may also contain an endothermic liquid. The magnetic resonance system may further include a ramping-down device configured to trigger releasing electric energy by the magnetic resonance magnet. The first ramping-down device may include an electric energy consumption device configured to consume at least a portion of the released electric energy by the magnetic resonance magnet.

A magnetic resonance system may include a magnetic resonance magnet and a storage container configured to accommodate the magnetic resonance magnet. The storage container may also contain an endothermic liquid. The magnetic resonance system may further include a ramping-down device configured to trigger releasing electric energy by the magnetic resonance magnet. The first ramping-down device may include an electric energy consumption device configured to consume at least a portion of the released electric energy by the magnetic resonance magnet.

A method of forming a crosslinked polyphenol, the method comprising: reacting a bio-based phenolic compound comprising at least one phenolic hydroxyl group, with a crosslinking agent comprising at least two functional groups reactive with the phenolic hydroxyl group, wherein the at least two functional groups are each independently a halogen group, acid halide group, sulfonyl halide group, glycidyl group, anhydride group, or a combination comprising at least one of the foregoing, to provide the crosslinked polyphenol.

A method of forming a crosslinked polyphenol, the method comprising: reacting a bio-based phenolic compound comprising at least one phenolic hydroxyl group, with a crosslinking agent comprising at least two functional groups reactive with the phenolic hydroxyl group, wherein the at least two functional groups are each independently a halogen group, acid halide group, sulfonyl halide group, glycidyl group, anhydride group, or a combination comprising at least one of the foregoing, to provide the crosslinked polyphenol.

A magnetic resonance system may include a magnetic resonance magnet and a storage container configured to accommodate the magnetic resonance magnet. The storage container may also contain an endothermic liquid. The magnetic resonance system may further include a ramping-down device configured to trigger releasing electric energy by the magnetic resonance magnet. The first ramping-down device may include an electric energy consumption device configured to consume at least a portion of the released electric energy by the magnetic resonance magnet.

A magnetic resonance system may include a magnetic resonance magnet and a storage container configured to accommodate the magnetic resonance magnet. The storage container may also contain an endothermic liquid. The magnetic resonance system may further include a ramping-down device configured to trigger releasing electric energy by the magnetic resonance magnet. The first ramping-down device may include an electric energy consumption device configured to consume at least a portion of the released electric energy by the magnetic resonance magnet.