DJG-1阳离子絮凝剂合成的影响因素

DJG-1阳离子絮凝剂的合成步骤为：玉米淀粉与丙烯酰胺在硝酸铈铵引发下接枝，得A；A与醇在酸催化下发生酯化反应得B；甲醛与二甲胺反应得N-羟甲基胺（C）；在C中加入酸使pH值为4左右。得酸性范围内的N-羟甲基胺（C′）。B与C′发生曼尼希反应得D（叔胺盐）；D发生烷基化反应E（季铵盐）；E与四苯硼钠反应生成白色沉淀。室内试验分析了DJG-1阳离子絮凝剂合成的影响因素。评价了DJG-1的水处理效果并与硫酸铝进行了对比。实验结果表明，DJG-1阳离子絮凝剂合成的影响因素包括引发剂的选用，活化时间，投料比，反应时间与温度及溶液pH值等。用DJG-1絮凝剂混凝处理钻井废水时，絮凝沉淀的速度比用硫酸铝处理时大得多，废水处理效率高，但DJG-1絮凝剂与硫酸铝复合使用经济效益更好，且硫酸铝用量为300mg/L时，DJG-1的最佳用量为3-4mg/L。     

Methacrylic acid–acrylamide-g-poly(ethyleneterephthalate) fibres for urea hydrolysis

This paper presents the results of urease immobilization onto methacrylic acid–acrylamide grafted poly(ethyleneterephthalate) fibres. The graft yield strongly affected the maximum activity of the immobilized enzyme up to a value of 70·2%. Higher grafting caused a decline in urease activity and led to the degradation of the fibres. The minor changes observed in K_m and V_max demonstrated that the conformational changes existed during immobilization were not extensive. However, 70·2% methacrylic acid–acrylamide-g-fibres containing urease were more stable towards acidic and alkaline pH, high temperature and storage conditions compared with free enzyme. Apart from the increase in stability to heat inactivation, the initial enzymatic activity of the urease–fibre system remained almost unchanged even after 40 repeated assays corresponding to 10 h of operation in 4 months, indicating the excellent durability of the system.     

聚烯烃塑料改性的研究进展

聚乙烯、聚丙烯以优良的力学性能、热性能、加工性能等成为最主要的聚烯烃塑料品种,大量用于生产薄膜、管材和板材。通过改性可获得高刚性、高强度、高耐热、低成本的聚烯烃塑料。综述了近年来聚乙烯和聚丙烯在接枝、交联、填充、共混等方面的改性进展,并指出了研究方向和发展趋势。     

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.     

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     

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。     

MAH接枝EPDM增韧PA66的研究

研究了MAH(马来酸酐)接枝三元乙丙橡胶(EPDM—g-MAH)对尼龙66(PA66)的增韧作用。利用SEM(扫描电镜)观察了共混体系的微观形貌(形态结构)，并运用小角激光散射(SALS)方法研究了EPDM的加入对PA66结晶性能的影响。结果表明，未接枝的EPDM与PA66的相容性很差，而EPDM—g—MAH与PA66相容性明显增加，EPDM-g—MAH粒子均匀分散在PA66中，共混体系力学性能有很大提高。随着EPDM—g—MAH用量的增加，PA66球晶尺寸变小，共混体系界面结合更加紧密。     

硅疏水改性聚胺阻垢剂的制备及其性能

用γ-缩水甘油醚氧丙基三甲氧基硅烷(KH560)、1-氯辛烷对低相对分子质量聚乙烯亚胺(PEI)进行疏水接枝改性,得到了含硅疏水改性聚胺阻垢剂。通过FTIR、TG、粒径分析、Zeta电位测试等分析改性后聚胺阻垢剂的结构与性能。结果表明,改性后产物热稳定性提高、黏度增大、表面张力降低、溶液粒径增大。将改性聚胺阻垢剂用于分散铝硅酸钠颗粒,对处理前后的颗粒进行红外光谱表征,并通过对悬浮分散液进行稳定性、颗粒沉降等测试,评价聚胺阻垢剂的阻垢分散性能并初步讨论其分散机理。当m(PEI, M_w=10000)∶m(KH560)∶m(1-氯辛烷)=10∶2∶0.5,反应时间6 h,反应温度75℃时,合成的阻垢剂分散性能最佳。当结疤的质量浓度为30 g/L时,悬浮液颗粒沉降速度达到最低值0.047 cm/d,沉降速率减小程度达到94.8%,分散性显著提高。经过改性后的PEI在氧化铝工业生产中具有高效的阻垢作用,可通过在工厂进行条件优化,进一步替代传统的强酸型阻垢剂,减小管道腐蚀程度,降低能耗。