层析法分离提取葡萄籽原花青素的进一步研究

以吸附量和解吸率为指标,比较了7种大孔吸附树脂对原花青素的静态吸附解吸性能并考查了AB—8树脂对原花青素的吸附特性及机理。实验结果表明:AB—8树脂是较理想的吸附剂;在溶液中AB—8树脂对原花青素的吸附达到平衡的时间为240 min,吸附行为符合Langmuir等温方程;最佳动态吸附参数原花青素提取液浓度4.0 mg/mL,吸附流速2 BV/h(1BV=13.03 mL)用40%乙醇溶液洗脱。AB—8树脂适合于柱层析操作分离原花青素。     

超声波提取-吸附分离-气相色谱法测定茶叶中农药残留

将超声提取-吸附分离的预处理技术用于气相色谱法检测茶叶中的农药残留。对超声波提取条件和吸附分离柱（自制）的结构进行了优化。建立了茶叶中有机磷类和菊酯类农药残留的气相色谱法定量测定的方法。进行了3个质量分数的标准添加，甲胺磷、乐果、联苯菊酯、氯氟氰菊酯、溴氰菊酯的回收率相应为75％～95％、87％～110％、89％-102％、88％-105％、80％-93％，相对标准偏差为2．6％．4．8％，检出限为0．005-0．02mg／kg。该方法速度快、灵敏度高、重现性好。     

(Ag)_核·(Au)_壳复合纳米粒子的制备

以银原子团簇作晶种,采用微波高压液相合成法制备了分散性好、规则球形的(Ag)核·(Au)壳复合纳米粒子。研究了(Ag)核·(Au)壳复合纳米粒子的紫外可见吸收光谱和共振散射光谱特性。结果表明,液相(Ag)核·(Au)壳复合纳米粒子和高压微波合成的液相金纳米粒子的最强共振散射峰均在580nm处,它们的吸收光谱图相似,最大吸收分别在518.5nm和524.8nm。     

The Estimation of the Molecular Weight of Polytetrafluoroethylene Based on the Heat of Crystallisation. A Comment on Suwa's Equation

Summary: The influence of number‐average molecular weight ranging from 1.4 · 10⁴ to 1.2 · 10⁶ g/mol on the thermal behaviour of polytetrafluoroethylene (PTFE) has been studied. Samples have been prepared by radiation‐induced degradation of commercial PTFE. The molecular weight has been calculated using end‐group concentration determined by infrared (IR) spectroscopy and ¹⁹F solid‐state nuclear magnetic resonance (NMR) spectroscopy. Melting and crystallisation heats were investigated by differential scanning calorimetry (DSC). The results have been discussed with respect to quantitative relationships between number‐average molecular weight and heat of crystallisation of PTFE described in the literature. The molecular weight calculated from Suwa's equation, which is often used in the literature, has been found to be too low.

Concentration of end‐groups and the molecular weight of PTFE versus the irradiation dose.     

微波辐射下一步合成2-甲氧基-3-氰基-4-芳基吡啶和2-氨基-3-氰基-4-芳基吡喃衍生物

2，5－双亚苄基环戊酮与丙二腈在氢氧化钠－甲醇或哌啶－乙醇中，经微波辐射一步合成了2－甲氧基－3－氰基－4－芳基吡啶和2－氨基－3－氰基－4－芳基吡喃衍生物，反应在3－9mi内完成，产率56％－78％。     

聚偏氟乙烯/聚丙烯酸酯复合乳液的合成与性能

在含氟表面活性剂存在下，将聚偏氟乙烯超声分散于甲基丙烯酸甲酯和丙烯酸丁酯的混合单体中进行乳液聚合，制备了聚偏氟乙烯／聚丙烯酸酯复合乳液。采用动态光散射DLS、透射电镜TEM和红外光谱FT—IR对乳液组成及乳胶粒子的形态进行了表征，并对聚合物胶膜的性能进行了测试分析。结果表明：聚偏氟乙烯的加入，使复合乳液膜的拉伸强度显著增大，吸水率减小。     

微波辐射下HPA快速催化合成丁酸异戊酯

在微波辐射下，以杂多酸HPA为催化剂，快速合成丁酸异戊酯，确定了酯化的优化条件。实验结果表明，醇酸物质的量比为1．9，催化剂用量为反应物料的1．O％，微波功率为800w，反应时间为20min，酯收率超过96％。     

超声波消除泡沫的研究

研究了超声波消除泡沫的原理，通过实验得出消泡时间、起泡剂浓度与频率之间的关系，从而为工业应用提供了重要的工艺参数。     

Electron beam irradiation of ethylene‐propylene terpolymer: Evaluation of trimethylol propane trimethacrylate as a crosslink promoter

The effect of electron beam irradiation on ethylene‐propylene terpolymer (EPDM) was investigated. A 50‐part oil‐extended EPDM with high termonomer (ENB) content (iodine number of base polymer) 19, was selected for this study. An increase in irradiation dose from 0 to 200 kGy resulted in increased crosslinking, measured by an increase in gel contents and better swelling resistance. The effect of the multifunctional monomer trimethylol propane trimethacrylate (TMPTMA) as a crosslink promoter was studied using IR spectroscopy. The IR studies revealed enhanced peak absorbances at 1725, 1257, and 1023 cm^?1 as a result of the increased concentration of C = O and C‐O‐C groups and reduced absorbance at 1630 cm^?1 due decreased concentration of C = C groups with TMPTMA level in the irradiated samples. The presence of TMPTMA increased the level of crosslinking at a given irradiation dose, which was manifested by improvement in tensile properties. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 968–975, 2005     

Photoinduced Polymerization in the Wall of Hollow Capsules

Summary: Novel light‐sensitive hollow capsules were fabricated from the small molecule 3‐sulfopropylacrylate potassium (SPA) and poly(allylamine hydrochloride) (PAH). With UV irradiation, SPA could be photopolymerized in the wall of hollow capsules. After photopolymerization the capsule size and surfaces showed pronounced differences. The capsules became much more rigid as indicated by an increase in the modulus of more than a factor of 5.

CLSM image of SPA/PAH hollow capsule emission at 554 nm, from rhodamine B after photopolymerization.