Abstract:
A poly(phenylene ether) resin composition includes a modified poly(phenylene ether) copolymer, a polymer substance having a weight-average molecular weight larger than that of the modified poly(phenylene ether) copolymer, and a compound compatible with the modified poly(phenylene ether) copolymer. The modified poly(phenylene ether) copolymer is produced by modifying the phenolic hydroxyl group in a molecular terminal of a poly(phenylene ether) copolymer with a compound having a carbon-carbon unsaturated double bond. The polymer substance has a structure of at least one selected from a polystyrene framework, a polybutadiene framework, and a methacrylate framework. The polymer substance has a softening temperature not higher than 110° C. The compound compatible with the modified poly(phenylene ether) copolymer includes two or more carbon-carbon unsaturated double-bonds per molecule, and has a melting point not higher than 30° C.
Abstract:
A prepreg includes a resin composition including: (A) at least one of an epoxy resin having a naphthalene skeleton and a phenolic hardener having a naphthalene skeleton; (B) a polymer having at least the structures of formulae (2) and (3) among formulae (1), (2) and (3) and having a weight-average molecular weight of from 200,000 to 850,000 inclusive; and (C) an inorganic filler: wherein x:y:z (molar fraction)=0:0.95:0.05 to 0.2:0.6:0.2 (where x+y+z≦1, 0≦x≦0.2, 0.6≦y≦0.95, 0.05≦z≦0.2); R1 represents a hydrogen atom or a methyl group and R2 includes at least one of a glycidyl group and an epoxidized alkyl group among a hydrogen atom, an alkyl group, a glycidyl group and an epoxidized alkyl group in formula (2); and R3 represents a hydrogen atom or a methyl group and R4 represents Ph (phenyl group), —COOCH2Ph or —COO(CH2)2Ph in formula (3).
Abstract:
A polyphenylene ether resin composition contains a modified polyphenylene ether copolymer and a high-molecular-weight compound. The modified polyphenylene ether copolymer is obtained by modifying a polyphenylene ether copolymer at a phenolic hydroxy group of a molecular chain end with a substituent having a carbon-carbon unsaturated double bond. The high-molecular-weight compound has a glass transition temperature (Tg) measured by differential scanning calorimetry of 20° C. or lower and has a number-average molecular weight Mn ranging from 1000 to 10000, inclusive. In a cured state of the polyphenylene ether resin composition, the modified polyphenylene ether copolymer is phase separated from the high-molecular-weight compound.
Abstract:
A metal foil with resin is a metal foil with resin including a metal foil and a resin layer disposed on the metal foil, resin layer being obtained by half-curing a resin composition. The resin composition contains a first component that is a polymer, a second component that is a polyarylene ether copolymer, and a third component that is an epoxy resin. The first component has structures represented by formulae (1) and (2) below, with no unsaturated bond between carbon atoms. The third component has two or more epoxy groups per molecule. The second component is compatible with the first component, and the third component is incompatible with the first component.In the formulae (1) and (2), a ratio between x and y is x:y=0:1 to 0.35:0.65, R1 represents hydrogen atom or methyl group, and R2 represents hydrogen atom or an alkyl group.
Abstract:
A prepreg includes a resin layer constituted by a half-cured product of a thermosetting resin composition, and a fibrous substrate provided in the resin layer. A prepreg test piece that is a cured product obtained by heat curing the thermosetting resin composition has a maximum value of 400 kPa or less for thermal shrinkage stress measured by a predetermined thermal stress test.
Abstract:
A prepreg satisfies the following properties (A) and (B).(A) The resin flow of the prepreg measured under conditions of 170° C. and 30 kgf/cm2 according to IEC 60249-3-1, 1981, is 0% or more and 5% or less.(B) In a dynamic viscoelasticity test under conditions of a temperature of 30° C. or higher and 200° C. or lower, a temperature rising rate of 3° C./min, and a frequency of 0.5 Hz, a relation of 1≦Vb/Va≦15 is established, where Va is a minimum melt viscosity of the resin composition collected from the prepreg, and Vb is a melt viscosity of the collected resin composition at a temperature Tb, Tb=Ta+20° C., and Ta is a temperature when the melt viscosity is the minimum melt viscosity Va.
Abstract translation:预浸料满足以下性能(A)和(B)。 (A)根据IEC60249-3-1,1981,在170℃,30kgf / cm 2的条件下测定的预浸料的树脂流量为0%以上且5%以下。 (B)在温度为30℃以上且200℃以下的动态粘弹性试验中,升温速度为3℃/分钟,频率为0.5Hz,关系为 1≦̸ Vb / Va≦̸ 15,其中Va是从预浸料收集的树脂组合物的最小熔融粘度,Vb是在Tb,Tb = Ta + 20℃的温度下收集的树脂组合物的熔体粘度。 ,Ta是当熔体粘度为最小熔融粘度Va时的温度。