新型聚丙烯酸(934P、980)树脂的制备

详细研究了以乙酸乙酯和环己烷为溶剂，丙烯酸为单体，BPO，LPO，AIBN为引发剂，聚烯基多醚为交联剂，合成增稠能力强、透明度高的聚丙烯酸树脂。于混和溶剂存在下制得的聚合物，消除了以往由二氯甲烷为溶剂的反应介质中所得产品的毒性，可广泛应用于医药及日用化工等行业。     

水溶性聚偶氮酯的研究

用Ｐｉｎｎｅｒ合成方法制备了用ＰＥＧ４００封端的水溶性聚偶氮酯，并表征了其结构；研究了热分解反应动力学及用于乳液聚合的动力学。结果表明，该种引发剂具有引发速度快、热分解机理简单和具有辅助乳化作用等优点。     

水溶液中硅酸溶解和胶结的实验研究

本研究了几种不酸ＰＨ值对硅酸胶结的影响。结果表明，草酸浓度增大时，硅酸胶结速度变缓，至ＰＨ３－４时，硅酸不再胶结；而ＨＣＬ浓度增大，虽然胶结速度变缓，但最终仍胶结。     

Radiation polymerization of acrylonitrile in a viscous system with styrene

Radiation polymerization of acrylonitrile in a viscous system with styrene was performed at ambient temperature by using γ‐rays. It is found that the overall rate of polymerization was accelerated after critical conversion due to the gel effect. As the molar fraction of styrene in monomer feed (f_St) is increased, both the total polymer conversion and molar fraction of acrylonitrile in the copolymer feed (F_AN) were decreased. The monomer reactivity ratios for acrylonitrile and styerne were determined to be r₁ (AN) = 0.25 and r₂ (St) = 2.0, respectively. The copolymers obtained were characterized by Fourier transformed infrared spectra (FTIR), X‐ray diffraction (XRD), scanning electron microscopy (SEM), ¹H‐NMR, and pyrolysis mass spectrometry (PMS). It was found that the slight addition of styrene to acrylonitrile strongly changes crystallinity, morphology, and thermal decomposition of the resulting polymer. ¹H‐NMR measurment of AN/St copolymer showed the appearance of aromatic proton signals and shifted the resonance of the methylene proton to lower chemical shifts. The mass spectra of AN/St copolymers showed fragments of pyrolysates corresponding to oligonitriles with styrene end groups. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 268–275, 2002; DOI 10.1002/app.10324     

高分子量阴离子型聚丙烯酰胺的制备

介绍了聚丙烯酰胺的品种、性能及用途；研究了以丙烯酸为共聚单体，采用反相乳液聚合制备高分子量阴离子型聚丙烯酰胺胶乳的原理和方法；分析讨论了原料纯度、乳化剂和引发剂种类及操作条件等因素对产品性能的影响．     

离子液体催化C_5馏分中二烯烃的聚合反应

合成了多种基于1-丁基-3-甲基咪唑阳离子的离子液体,并作为裂解C5馏分中混合二烯烃聚合反应的介质。考察了离子液体种类、反应温度、反应时间和添加Lew is酸对混合二烯烃聚合反应的影响。实验结果表明,以硝酸根为阴离子的离子液体对混合二烯烃的聚合反应具有一定的阻聚作用;以六氟磷酸根为阴离子的离子液体能明显促进混合二烯烃的聚合反应,提高二聚物的含量;添加Lew is酸(质量分数为1%的ZnCl2)的离子液体对混合二烯烃的聚合反应具有更明显的促进作用,其效果仅次于酸性氯铝酸类离子液体,反应温度以30℃以下为宜,温度过高将促使二聚物进一步聚合,形成三聚物乃至多聚物,降低二聚物的含量。     

Photoinitiated cationic polymerization using a novel phenacyl anilinium salt

A novel phenacyl anilinium salt, N-phenacyl, N,N-dimethylanilinium hexafluoroantimonate, (PDA), has been synthesized and used as photoinitiator for cationic polymerization of cyclohexene oxide (CHO), butyl vinyl ether (BVE) and N-vinyl carbazol (NVC). Plausible mechanism of the photoinitiation involves the decay of the excited PDA with both heterolytic and homolytic cleavages of carbon-nitrogen bond. Thus, phenacylium cations formed directly or subsequent intermolecular electron transfer, respectively, initiate the polymerization.     

γ 射线引发 VAc 乳液聚合以制备白乳胶的动力学及工艺条件研究

研究了ＶＡｃ的辐射乳液聚合动力学，并对其聚合工艺条件作了初步探索。得出ＶＡｃ乳液在进行辐射聚合时，成核期结束较早（转化率在１０％以下），有相当长的恒速期存在。乳胶粒子直径在０．５～３μｍ之间，比一般的乳液聚合乳胶粒子要大。同时从动力学数据还可以看出几种成核机理（胶束成核，水相成核和液滴成核）同时存在，由此对试验条件提出了相应的要求。     

背包问题最优解的结构

讨论背包问题的最优解,引入背包问题的阶的概念,并对背包问题的阶作出深入的讨论,在此基础上得到背包问题的最优解的一般形式。     

FTIR investigation of ethylene coordination and polymerization on reduced Cr/SiO2 catalyst

FTIR spectroscopy was applied to study the initial steps of ethylene polymerization on reduced chromia-silica (0.5 wt% Cr/SiO₂). To decrease the speed of the reaction small doses of gas were introduced to the catalyst in each run and C₂D₄ was used to confirm band assignments. At the initial steps of the reaction only ethylene molecules coordinated to probably Cr _A ²⁺ cations were observed. The concentration of such complexes was estimated to be about 50% of the total amount of Cr atoms in the sample. The FTIR spectrum of the polymer formed at the initial doses of C₂H₄ (when [C₂H₄] [Cr]) was found to be slightly different from that formed after excess ethylene was introduced onto the catalyst ([C₂H₄] > [Cr]).