改性淀粉与丙烯酸接枝共聚物的合成及应用性能

研究经过热处理的改性淀粉与丙烯酸的接枝共聚反应。接枝共聚产物在 790cm-1、85 0cm-1(物理改性淀粉的特征吸收峰 )和 172 0cm-1(聚丙烯酸的特征吸收峰 )处的红外光谱验证了接枝共聚反应的发生。探讨了引发剂过硫酸铵浓度、丙烯酸浓度、反应温度和反应时间等因素对接枝率和接枝效率的影响。当 ρ(淀粉 ) =70 g/L、t =6 0℃、反应时间为 3h、c〔(NH4) 2 S2 O8〕 =3 0× 10 -3 mol/L、c(丙烯酸 ) =0 4 2mol/L时 ,合成胶粘剂的初粘力为 10 0 % ,吸水率为 15 0 14 % ,吸油率为 2 0 6 % ,其压制的纸板冲击强度为 3 2 5kN/m ,拉伸强度为 3 75MPa ,与纯淀粉粘接剂相比较 ,所压制纸板的应用性能得到较大的改善。     

氧气法合成乙醛酸的中试研究

中试结果表明 ,在复合催化剂作用下 ,用低压氧气氧化乙二醛水溶液 ,可成功合成乙醛酸。电位滴定跟踪反应过程 ,可满意监控乙二醛反应程度。此反应乙二醛转化率 99% ,乙醛酸收率(以乙二醛为基准 ) 94 %。优化工艺为 :介质 pH <1,釜内氧气、水气等混合气体总压 0 12～ 0 13MPa ,w(乙二醛 ) =15 5 6 % ,反应温度 4 5～ 6 0℃ ,时间 4h。     

Studies on the semirigid chain polyamide—poly(1,4-phenyleneterephthalamide)

In this article, the polycondensation of terephthaloyl chloride and p-phenylenediamine was systematically studied, including the liquid–crystalline state of the solution and the spinning of poly(1,4-phenyleneterephthalamide) (PPTA). High-molecular-weight PPTA with ε_inh = 5–7 was prepared and the main factors influencing the solution polycondensation of 1,4-phenylenediamine with terephthaloyl chloride were studied in detail. Experimental results showed that the water content of the reaction system, reactant concentration, and volume ratio of mix solvents have a great influence on the inherent viscosity of the poly(1,4-phenyleneterephthalamide) obtained. The highest ε_inh was obtained at 0.3M/liter reactant concentration in a mixed solvent ratio HMPA/DMAC of 4/1 (by volume), at 0.35M/liter reactant concentration in a mixed solvent of HMPA/NMP = 7/3, and at 0.5M/liter of reactant concentration in a mixed solvent of HMPA/THF = 9/1. The water content must be controlled to less than 100 ppm in the polymerization system. In the early stage of the polycondensation process, the ε_inh of the polymer obtained increased rapidly with time. The system gelled within 2 or 3 min, while the monomer conversion reached about 100%. However, the reaction of polycondensation continued after gelation and the ε_inh of the polymer increased appreciably. We have studied the viscosity behavior at 20–155°C for the anisotropic solution of PPTA in 100% sulfuric acid (ε_inh of PPTA 2.5–4.9). Experimental results showed that, at low concentrations the viscosity of isotropic solution increases with the increase of polymer concentration to reach a maxium near the critical polymer concentration, beyond which the solution changes to an anisotropic liquid–crystalline solution. The appropriate spinning region was obtained as shown in the phase diagram determined by viscosity, degree of depolarization anisotropy, and region of thermal depolymerization. Fibers of PPTA with high modulus and high tenacity were obtained by dry-jet wet spinning. The fibers obtained have a tenacity of ～22 g/denier, a modulus of ～600 g/denier, and elongation at break ～3.5%.     

Effect of molecular weight on two smectic polyesters

The liquid crystalline transitions of two kinds of smectic polyesters with different molecular weights were investigated by DSC, polarized microscopy and X-ray diffraction. The molecular weight affects the transitions significantly for these two kinds of polyesters. With a high enough molecular weight, both poly (pentamethylenep,p-bibenzoate) and poly(hexamethylenep,p-bibenzoate) exhibit an enantiotropic smectic phase, but the two endothermic transition peaks of the DSC heating curve seem to overlap. The polyesters tend to exhibit a monotropic smectic phase as the molecular weight decreases. From the DSC cooling curve, the isotropic-smectic transition can be seen more clearly. As the molecular weight decreases, the smectic order decrease significantly. The molecular weight affects the transitions in a different way for these two different kinds of polyesters.     

浸渍增重率和反渗率研究

对浸溃过程中浸渍剂沥青的浸入率和反渗率进行了分析与探讨。提出了理想增重率、理论增重率与实际增重率的概念和计算方法。并比较了实际增重率与操作增重率的差别。同时分析了抽真空的绝对压力与施压的绝对压力对各项增重率和反渗率的影响。     

硫化机网络群控系统

对硫化机群采用分散控制-集中管理式中央监控系统.系统分底层网络和上层网络两部分.底层网络分二级控制,采集现场硫化机温度、压力等参数.上层网络用于对生产数据进行处理显示、打印报表等.各层控制系统实现相对独立,该系统运行多年,未发生异常现象.     

Preparation and characterization of high-surface-area titanium dioxide by sol-gel process

One of the important ways to improve photocatalytic efficiency is to prepare catalyst with enhanced surface area. In this work, titanium dioxide (TiO₂) nanoparticles having enhanced surface area were synthesized under the interference of SiO₂. The mixed oxide, SiO₂-TiO₂ (10% mol% Si), was prepared by a sol-gel procedure using titanium tetra-n-butoxide as Ti-precursor. The commercial SiO₂ nanoparticles were added into the TiO₂ sols after hydrolysis. After condensation and calcination heat treatment, the SiO₂-TiO₂ nanoparticles were obtained. To achieve the purpose of obtaining the high-surface-area TiO₂, the SiO₂ was removed subsequently by aqueous NaOH solution. The TiO₂ products were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), electron spectroscopy for chemical analysis (ESCA), and by N₂ adsorption-desorption isotherm. A fine mesoporous structure was formed for as-prepared TiO₂ after calcination at 400^∘C and the average pore diameter was about 7 nm. The porous TiO₂ products possess mixing phases of anatase and rutile. Phase transformation from anatase to rutile occurred when the samples were calcined. The phase transition temperature is sensitive to the silicon content. The particle size of ∼43 nm remained constant upon calcinations from 500 to 700^∘C. The specific surface area was increased up to 66% compared to regular TiO₂ samples that were prepared by the similar sol-gel procedure. The porous TiO₂ nanostructures exhibited enhanced photocatalytic performance to decompose methylene blue under UV irradiation.     

Effect of Cr3C2 on Valence-Electron Structure and Plasticity of Rim Phase in Ti(C,N)-Based Cermets

Based on the empirical electron theory of solids and molecules, the valence-electron structure (VES) of the rim phase in Ti(C,N)-based cermets was calculated, and the relationship between the VES and plasticity was determined. The results indicated that the plasticity of the rim phase in a Ti(C,N)-based cermet could be defined using the sum of the n _a values for the covalent bonds, and that chromium dissolution in the rim phase improved the plasticity of the rim phase. Moreover, a series of experiments showed that adding Cr₂C₃ to a typical Ti(C,N)-based cermet strengthened the interface. Based on those results, a Ti(C,N)-based cermet with added Cr₃C₂ was manufactured; the new cermet had more than twice the transverse rupture strength of a typical cermet.     

力化学法制备金属－NR硫化粘合用CSM－NR接枝聚合物

用开炼机，通过力化学方法，将ＮＲ／ＣＳＭ（质量比为１０／９０）制成４５￣＃钢－ＮＲ硫化粘合剂用接枝聚合物。当橡胶本体１００％破坏时，１８０°剥离强度为２３．６～２４．６ｋＮ／ｍ。     

废水处理中的复极性固定床电解槽技术

复极性固定床电解槽（bipolar packed bed cell,BPBC)是在三维电极原理基础上发展起来的新型电化学工程技术，其在治理含氰及重金属废水、有机废水和印染废水方面具有良好的处理效果。介绍了BPBC的电化学特性，综述了国内外BPBC废水处理技术应用现状及其机理研究的概况。同时，提出了该技术目前存在的问题，并对其进一步的深入研究作了展望。