Tertiary amine-mediated synthesis of microporous carbon membranes

Microporous carbon membranes were prepared on an -alumina support by a pyrolysis of cationic tertiary amine/anionic polymer composites. The precursor solutions contain a thermosetting resorcinol/formaldehyde (RF) polymer and a cationic tertiary amine. Three types of cationic tertiary amines with different chain lengths were used, such as tetramethlammonium bromide (TMAB), tetrapropylammonium bromide (TPAB) and cetyltrimethylammonium bromide (CTAB). A porous structure was produced by a decomposition of the amine and the resulting pores assisted the further gasification of the RF polymer at high temperature. The carbon/alumina membranes have thin and continuous carbon top layers with a thickness of 1 μm. Gas permeation tests were performed using single gases of CO₂, O₂, N₂, CF₄, n-C₄H₁₀ and i-C₄H₁₀, as well as binary mixtures of CH₄/n-C₄H₁₀ and N₂/CF₄ at different temperatures between 23 and 150 °C. The carbon membrane prepared using TMAB showed separation factors higher than 650 for the CH₄/n-C₄H₁₀ mixtures and higher than 8100 for the N₂/CF₄ mixture. From the permeation of pure gases with different molecular sizes, the pore sizes of the carbon membrane prepared using TMAB, TPAB and CTAB are estimated to be 4.0, 5.0 and larger than 5.5 Å, respectively, indicating that the micropore size of the carbon membranes is controllable by using different amines.     

Self-ordering process of phenanthrene polyesters observed by the simultaneous DSC-XRD method

Phase transition behavior of polyesters derived from 2,7-phenanthrene dicarbonic acid diethylester and alkanediols with even methylene carbon number was investigated by the simultaneous DSC-XRD method. The smectic A phase was observed on cooling from the molten state. The transition entropy from the isotropic state to the smectic A phase was about 9.0 J mol^-1 K^-1, which depended on the methylene carbon number. The linear expansion coefficients, based on the (001) spacing of the crystalline phase at room temperature, were 1.3·10^-4 K^-1 (crystalline phase), 5.7·10^-4 K^-1 (crystallization region), 1.7·10^-3 K^-1 (smectic A phase) during cooling, and 1.5·10^-4 K^-1 (crystalline phase), and 1.0·10^-3K^-1(melting region) on heating. This revised version was published online in July 2006 with corrections to the Cover Date.     

活性酚醛树脂中羟甲基含量的测定

本文提出一种酚醛树脂中羟甲基含量的化学分析法，分别以＾１３ＣＮＭＲ和化学分析法测定酚醛树脂的羟甲基含量。将两种测试结果与已知的投料量进行比较，证明所建立的化学分析法可行。     

强酸阳离子交换树脂催化性能的研究

通过叔丁醇脱水生成异丁烯的反应研究对比了国内外常见种类的凝胶型和大孔型强酸阳离子交换树脂的催化性能，并对树脂的性质，预处理方法，以及其用量和再生程度等因素对树脂催化活性的影响进行了研究。在此基础上，合成了具有较高催化活性的新型大孔强酸阳离子交换树脂。     

纤维素基磁性聚偕胺肟树脂的研究——循环吸溴中吸附与还原能力的变化

研究了酸式纤维素基磁性聚偕胺肟树脂（ＡＭＡＯ）在循环吸溴过程中吸附容量和还原能力的变化，发现原树脂的吸溴初速和溴的还原率比再生树脂高一倍以上，但第一次和第二次再生树脂的吸附速度和还原效率几乎相同，暗示着树脂吸溴后基本结构已发生了彻底的变化．树脂在循环使用时吸溴容量变化不大而溴的还原量却显著降低，表明ＡＭＡＯ作为吸溴剂有较高的实用价值．     

Solubilities,thermostabilities and flame retardance behaviour of phosphorus-containing flame retardants and copolymers

Thirteen phosphorus-containing flame retardants were synthesized in this work. The solubilities of flame retardant [(6-oxide-6H-dibenz[c,e][1,2]oxaphosphorin-6-yl)-methyl]-butanedioic acid (DDP) in selected solvents are measured. TGA measurements of the 13 phosphorus-containing flame retardants were carried out and thermal stabilities of three flame-resistant PET (FRPET) resins were investigated. A FRPET incorporated by DDP with terephthalic acid and ethylene glycol reported in literature was also discussed and compared. The thermal stability of the FRPET is improved by the incorporation of phosphorus-containing flame retardants. The LOI values of all phosphorus-containing polyesters are higher than 27%. The improvement of the flame-resistant ability is due to the formation of the char that is not only caused by the existence of phosphorus elements in the resin but also by the relative large number of carbon atoms of the phenyl group in the flame retardants.     

离子交换树脂纯化酪蛋白磷酸肽研究

通过单因素实验和正交试验确定了使用D-201型大孔强碱性阴离子交换树脂纯化酪蛋白磷酸肽(CPPs)的操作条件为：洗脱温度40℃、洗脱酸(HCI)浓度0．2mol／L、洗脱速度2．3ml／min、进样浓度2％(w／v)，进一步应用HPSEC技术分析考察了离子交换树脂纯化后含磷洗脱峰分子量分布情况，并计算了产品氮磷比与纯化收率．     

D072型树脂脱除过氧化氢中金属阳离子的工艺研究

实验考察D072型阳离子交换树脂在交换柱中脱除过氧化氢中微量金属阳离子的动态行为．通过改变料液流速、高径比、料液中交换离子浓度及料液组成等参数，绘制不同条件下的透过曲线，以此考察D072型树脂对过氧化氢中金属阳离子的动态交换性能，从而确定适宜的工艺条件，为工业化生产提供科学依据．     

高折光指数光学树脂的合成——相转移法合成不饱和硫醇酯单体的条件控制

采用正常的低温相转移催化（ＰＴＣ）和反滴碱溶液ＰＴＣ法分别合成了含硫双烯ＭＥＳＤＭＡ和单烯ＭＥＰＳＭＡ．１Ｈ ＮＭＲ分析证明ＭＥＳ中的杂质主要是由原料ＴＤＧ引入的．对含单个巯基的ＭＥＰＳ的正常ＰＴＣ酯化接枝双键，因存在巯基和不饱和双键的加成反应而导致失败．作者最终得到了折光指数在１６２５以上的ＭＥＳＤＭＡ／ＭＥＰＳＭＡ共聚物．     

不饱和链烃沸点的拓扑研究

基于邻接矩阵与边价 (fi)定义边价连接性指数 ( mF) ,其中的0 F ,1 F与 2 94种不饱和链烃 (包括烯烃、炔烃及烯炔烃 )的沸点 (Tb)关联 ,得到良好的数学模型 :ln( 70 0 -Tb) =6 5 2 3 3 1-0 0 0 4880 F2 -0 3 46771 F0 5(n =2 94,R =0 9979,R2 =0 995 8,F =3 490 4,S =5 12 ) ,该回归模型经Jackknife法检验具有总体稳健性 .可以预示 ,该指数将在定量构效关系研究中成为重要参数 .