氯丁橡胶的溶液接枝反应研究

本文研究了引发剂过氧化苯甲酰的用量对ＣＲ接技ＭＭＡ－ＡＡ反应的单体转化率、接枝率及接枝胶的粘度、剥离强度等的影响，并用红外光谱和元素和元素分析对反应产物进行了表征．结果表明，体系中存在接枝、降解、交联三种反应，在不同的配方和工艺条件下，三种反应的反应程度不同．     

In Situ FTIR Study of the Formation of an Organosilane Layer at the Silica/Solution Interface

An FTIR experiment especially designed to study the growth of an organosilane layer at the interface between a solution and a flat silica surface is presented. High sensitivity is achieved by using the attenuated total reflection (ATR) technique in a liquid flow cell. The ATR crystal, either silicon or germanium, is covered with a very thin silica layer. Chemical reactions of a mono-and a di-hydrolyzable silane with the silica substrate have been investigated. The grafting of a submonolayer of the first reagent has been monitored by following the C-H and SiO-H vibrations. The density of grafted molecules has been estimated and information on the nature of the chemical bonding has been achieved. Evidence for the chain-polymerization of the dihydrolyzable silane at the substrate/solution interface has been inferred from the appearance of a Si-O-Si absorption band.     

VAc／MMA半连续乳液共聚合的研究：Ⅱ分子量及其分布

以过硫酸铵为引发剂，十二烷基硫酸钠为乳化剂，于７０℃下进行了ＶＡｃ／ＭＭＡ乳液共聚合试验。试验确定了不同组成ＶＡｃ／ＭＭＡ共聚物的Ｍａｒｋ－Ｈｏｕｗｉｎｋ方程参数Ｋ和α值。对ＧＰＣ测试数据处理给出了加料速率，乳化剂量，单体比例及种子与非种子法对分子是及其分布的影响。     

Fluorinated Polyphosphazenes: A Survey

A general survey of fluorinated phosphazene polymers starting from their synthesis in 1965 to recent times is presented. Various types of fluorinated phosphazenes are described depending on the way fluorine atoms are connected to the polyphosphazene skeleton. The characterization, properties and practical utilization of these compounds in different domains are critically discussed.     

血液过滤用熔喷PBT非织造布紫外辐照接枝改性研究

研究了血液过滤用熔喷PBT非织造布的紫外辐照气相接枝改性方法。通过实验选择了丙烯酸(AAc)为接枝单体 ,探讨光照时间、预辐照时间、单体温度、引发剂浓度、氮气压力对接枝率和表面润湿张力的影响 ,结果得到最佳的紫外辐照接枝条件为 :室温下 ,光距 2 0cm ,预浸 10min ,二苯甲酮 (BP) 0 .0 37mol/L ,冲入单体的氮气流量 87.5h/L ,反应时间 30min。PBT非织造布AAc紫外辐照接枝后表面润湿张力可以达到 85mN/m左右 ,且表面润湿张力随接枝率的提高而增加     

Copolymerization in UF/pMDI adhesives networks

Kinetic evidence in thermomechanical analysis experiments and carbon‐13 nuclear magnetic resonance spectroscopy (¹³C NMR) evidence indicates that the strength of a joint bonded with UF (urea–formaldehyde)/polymeric 4,4'‐diphenylmethane diisocyanate (pMDI) glue mixes is improved by coreaction of the methylol groups of UF resins with pMDI to form a certain number of methylene cross‐links. The formation of these methylene cross‐links is predominant, rather than formation of urethane bridges which still appear to form but which are in great minority. This reaction occurs in presence of water and under the predominantly acid hardening conditions, which is characteristic of aminoplastic resins (thus, in presence of a hardener). Coreaction occurs to a much lesser extent under alkaline conditions (hence, without UF resins hardeners). The predominant reaction is then different in UF/pMDI adhesive systems than that observed in phenol‐formaldehyde (PF)/pMDI adhesive systems. The same reaction observed for UF/pMDI system at higher temperatures has also been observed in PF/pMDI systems, but only at lower temperatures. The water introduced in the UF/pMDI mix by addition of the UF resin solution has been shown not to react with pMDI to an extent such as to contribute much, if at all, to the increase in strength of the hardened adhesive. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 3681–3688, 2002     

拟活性阳离子聚合——异丁烯与苯乙烯嵌段共聚物的合成与表征

以丙烯酸正丁酯-四氯化钛-二甲基亚砜为引发体系,于二氯甲烷中、-45℃下进行异丁烯与苯乙烯的拟活性阳离子嵌段共聚反应。结果表明,选择适当的反应条件,可得到两单体的共聚效率为50％,共聚物中平均苯乙烯结合量为31.7％(质量),分子量为3万,分子量分散指数约为1.8的嵌段共聚物。     

聚丙烯固相法接枝改性

聚丙烯固相法接枝不饱和单体是一种简便易行的本体法技术。与其它接枝方法相比，具有成本低、接枝率高、时间短、无溶剂回收、不妨害接枝物的进一步应用等优点。本文介绍了聚丙烯固相法接枝不饱和单体的进展，并较详细地讨论了影响接枝反应的各种因素。     

Miniemulsion and conventional emulsion copolymerization of styrene and butadiene: Effect of process on gel content

The properties of styrene/butadiene copolymers obtained by conventional emulsion and miniemulsion polymerizations were studied. Thin layer chromatography with flame ionization detection was used to determine the gel fraction of the copolymer in the latex particles as a function of conversion. It was found that the gel formation began at a higher conversion in the miniemulsion polymerization when compared with that in the conventional process. Also, a lower glass transition temperature was noted at the lowest conversion sampled (～25%), implying a higher initial butadiene monomer concentration within the nucleated miniemulsion monomer droplets when compared with particles formed conventionally. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4616–4622, 2006     

超细纤维素胶体和丙烯酰胺的接枝共聚

本文用纤维素材料经酸分解制备具有平衡聚合度（LODP）的微晶纤维素，再分散成超细纤维素胶体（准均相纤维素体系）。用扫描电镜（SEM）观察处理前后的纤维素颗粒尺寸，并比较它们和丙烯酰胺接枝共聚的反应速率、聚合转化率、接枝率、接技效率、聚丙烯酰胺支链的分子量及其分布的情况。