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71.
Physical ageing rates of poly(ethylene terephthalate) have been measured, and ageing is interpreted to be associated with the conventional glass formation process, which occurs at a more rapid rate at higher temperatures. Ageing is accompanied by a marked change in mechanical properties, increased tensile yield stress and drawing stress, more localized yielding of the polymer and a marked decrease in impact strength. The fracture results have been attributed to the increased yield stress and a change in contribution of plane stress and plane strain conditions in the samples. Fracture surfaces show evidence of mixed modes of fracture. 相似文献
72.
Transport in ternary polymer1, polymer2, solvent systems has been investigated using an n.m.r. spin-echo technique. The dependence of the self-diffusion coefficient of poly(ethylene oxide) polymers on the concentration and molecular size of dextran in aqueous solution has been measured. Monodisperse poly(ethylene oxide) fractions (, 2.8·105 and 1.2·106) and dextrans (, 1·105 and 5·105) have been employed over a range of concentration up to the miscibility limit in each system. It is found that when the molecular size of the diffusant is commensurate with or exceeds that of the matrix polymer, a relationship of the form: is applicable, where C[η] refers to the dextran component and is considered to describe the extent of coil overlap in concentrated solution. () is independent of the molecular size of the poly(ethylene oxide), at least in the range studied (Mw<300 000). 相似文献
73.
The complexation between poly(ethylene oxide) (PEO) and poly(acrylic acid) (PAA) was made by using double the molar quantity of either polymer component at pH 2 where the resulting complex completely precipitates. After the removal of the precipitate, PEO or PAA remaining in the supernatant was subjected to gel permeation chromatography to investigate the change in the molecular weight distribution (MWD) caused by the complexation. No remarkable difference is observed in the MWD curves for PEO[1] (Mw=1.37 × 104) before and after the complexation with PAA[1] (Mw=1.10 × 103) and PAA[2] (Mw=4.16 × 105). However, the MWD curves of PEO[2] (Mw=1.26 × 105) and PAA[2] become shortened and shift to the low molecular weight side after the complexation with PAA[1] or [2] and PEO[2], respectively. This tendency is enhanced by increasing the complexation temperature. From these results, it is indicated that the complexation between PEO and PAA deals with an equilibrium reaction, and the equilibrium constant is dependent on the chain length of both polymer components and also on the complexation temperature. 相似文献
74.
This study was undertaken to elucidate the state of a polymer in the amorphous state through a change of motion of the molecular chain caused by heat treatment below the glass transition temperature. From dielectric measurements of amorphous poly(ethylene terephthalate) heat-treated below Tg, it was found that the average relaxation time, the distribution of relaxation time and the dielectric strength increase with increase of heat treatment. From these results, it was concluded that the amorphous state becomes more random by heat treatment. 相似文献
75.
76.
利用碳酸乙烯酯(EC)为液化剂在常压条件下对油菜秸秆进行了液化试验。选择甲烷磺酸(MSA)作为最优催化剂,探讨了反应温度、反应时间、物料量、催化剂量4个因素对液化得率及黏度的影响。采用二次回归正交旋转组合设计对其液化工艺进行了优化。结果表明:最佳液化条件为反应温度165℃,反应时间70 min,物料量15.5%,催化剂量3.2%。在此条件下,液化得率可达到92.89%。 相似文献
77.
78.
79.
预处理对增加红富士苹果细胞壁物质降解和出汁率的影响 总被引:1,自引:1,他引:1
为了通过简便易行的预处理增强果实细胞壁物质降解,提高苹果果实出汁率。文中测定了500mg/L乙烯利(E_1)和100mg/L乙烯利配合60℃热水(E_2)处理,对红富士果实堆放期细胞壁酶活性、细胞壁物质含量和出汁率的影响。结果表明:E_1使其果胶甲酯酶(PME)、纤维素酶(CS)活性高峰分别比对照提前6、3d,多聚半乳糖醛酸酶(PG)活性在前15d持续高于对照,木聚糖酶(Xyl)活性基本不变;处理12d后,果实细胞壁多糖中果胶类多糖、半纤维素类多糖和细胞壁残渣多糖含量分别下降到对照的80.1%、70.4%和75.7%;处理后9~18d,红富士苹果的出汁率较对照提高2.3%~4.0%;E_2抑制了果实PME活性,却普遍增强了0~6d内PG、Xyl、CS活性,亦促进了各类细胞壁物质的降解,0~9d内果实出汁率较对照高3.2%~7.1%。 相似文献
80.