Abstract:
A polyester elastomer is provided, which includes a product of reacting (a) amide oligomer, (b) polyalkylene glycol, and (c) poly(alkylene arylate). (a) Amide oligomer has a chemical structure of or a combination thereof, wherein R1 is C4-8 alkylene group, R2 is C4-8 alkylene group, and each of x is independently an integer of 10 to 20. (b) Polyalkylene glycol has a chemical structure of wherein R3 is C2-10 alkylene group, and y is an integer of 20 to 30. (c) Poly(alkylene arylate) has a chemical structure of or a combination thereof, wherein Ar is R4 is C2-6 alkylene group, and z is an integer of 1 to 10.
Abstract:
A polyester film is provided. The polyester film is produced from a composition that includes the following monomers: terephthalic acid, ethylene glycol, and a branched monomer having a structure represented by formula (I), formula (II) or formula (III): , wherein X is independently hydroxyl, carboxyl or —COOR, and R is C1-6 alkyl. The molar ratio between terephthalic acid and ethylene glycol ranges is between about 50:50 and 30:70. The molar percentage of the branched monomer is from about 1 mol % to 3 mol %, based on the total mole of terephthalic acid and ethylene glycol.
Abstract:
The disclosure provides a masterbatch, a method for fabricating the same and a film formed from the masterbatch. The masterbatch includes a product prepared from a composition via polymerization and granulation. The composition includes: terephthalic acid; and a silicon dioxide dispersion, wherein the silicon dioxide dispersion includes surface-modified silicon dioxide particles disposed within ethylene glycol, and the surface-modified silicon dioxide particle has first functional groups and second functional groups bonded on the surface of the silicon dioxide particles, wherein the first functional groups have a structure represented by and the second functional groups include a C1-8 haloalkyl functional group, C1-8 alkoxy functional group, C1-8 aminoalkyl functional group, C2-8 alkenyl group, or epoxy group, R1 is hydrogen or a C1-3 alkyl functional group, and n is 1-4.
Abstract:
A liquid crystal polymer, composition, liquid crystal polymer film, laminated material and method of forming liquid crystal polymer film are provided. The liquid crystal polymer includes a first repeating unit, a second repeating unit, a third repeating unit, a fourth repeating unit, and a fifth repeating unit. The first repeating unit has a structure of Formula (I), the second repeating unit has a structure of Formula (II), the third repeating unit has a structure of Formula (III), the fourth repeating unit has a structure of Formula (IV), and the fifth repeating unit has a structure of Formula (V), a structure of Formula (VI), or a structure of Formula (VII)
wherein A1, A2, A3, A4, X1, Z1, R1, R2, R3 and Q are as defined in the specification.
Abstract:
A liquid-crystal polymer includes at least one repeating unit having a spiro structure, and the repeating unit occupies 1 mol % to 20 mol % of the liquid-crystal polymer. The liquid-crystal polymer is composed of the following repeating units: 1 mol % to 20 mol % of 10 mol % to 35 mol % of 10 mol % to 35 mol % of 10 mol % to 50 mol % of and 10 mol % to 40 mol % of AR1 is wherein each of ring R and ring S is independently a C3-20 ring, ring R and ring S share a carbon atom, and each of K1 and K2 is independently a C5-20 conjugated system. Each of AR2, AR3, AR4, and AR5 is independently AR6 or AR6—Z—AR7.
Abstract:
A method for preparing an aromatic sulfide or a salt thereof is provided. The method for preparing an aromatic sulfide or a salt thereof includes reacting a compound having a structure represented by Formula (I) to a compound having a structure represented by Formula (III) in the presence of a compound having a structure represented by Formula (II) to obtain a compound having a structure represented by Formula (IV) wherein R1 and R2 are independently C1-6 alkyl group, or C5-7 cycloalkyl group; R3 is independently C1-6 alkyl group, C5-7 cycloalkyl group, C1-6 haloalkyl group, or aryl group; R4 is independently H, or C1-6 alkyl group; Y is H, aryl group, or —X—R5; X is —O—, —NH—, —PH—, or —S—, or Y and an adjacent R4 are optionally combined with the carbon atoms to which they are attached, to form an aryl group; and R5 is H, C1-6 alkyl group, C5-7 cycloalkyl group, or aryl group; and Z− is R3SO3−.
Abstract:
A liquid crystal polymer, composition, liquid crystal polymer film, laminated material and method of forming liquid crystal polymer film are provided. The liquid crystal polymer includes a first repeating unit, a second repeating unit, a third repeating unit, and a fourth repeating unit. The first repeating unit has a structure of Formula (I), the second repeating unit has a structure of Formula (II), the third repeating unit has a structure of Formula (III), and the fourth repeating unit has a structure of Formula (IV), a structure of Formula (V) or a structure of Formula (VI)
wherein A1, A2, A3, Z1, R1, R2, R3 and Q are as defined in the specification.
Abstract:
A method for preparing a polymer is provided. The method for preparing a polymer includes subjecting at least one monomer having a structure represented by Formula (I) to a reaction in the presence of sulfonic acid, diphenyl amine, and oxygen-containing phosphide, obtaining a sulfonium salt polymer wherein x is 0, 1, or 2; R1 is C1-6 alkyl group; and R2 is independently hydrogen, or C1-6 alkyl group. In particular, the molar ratio of the diphenyl amine to the oxygen-containing phosphide is from 4:1 to 1:1.
Abstract:
A method for preparing a polymer is provided. The method for preparing a polymer includes subjecting at least one monomer having a structure represented by Formula (I) to a reaction in the presence of sulfonic acid, diphenyl amine, and oxygen-containing phosphide, obtaining a sulfonium salt polymer wherein x is 0, 1, or 2, R1 is C1-6 alkyl group; and R2 is independently hydrogen, or C1-6 alkyl group.
Abstract:
A polymer is provided. The polymer has a repeating unit having a structure represented by Formula (I) or Formula (II) wherein Ar1 and Ar2 can be substituted or unsubstituted aryl diradical; Y− can be R2SO3− or ClO4−; R1 can be C1-6 alkyl; Ar1 and Ar2 are different; and, R2 can be C1-6 alkyl, substituted or unsubstituted aromatic ring, or C1-6 haloalkyl.