Ca_(0.6)Mg_(0.4)Zr_4(PO_4)_6低膨胀陶瓷的制备与烧结

采用分步沉淀法合成了Ca_(0.6)Mg_(o.4)Zr_4(PO_4)_6单相粉体。CMZP陶瓷的烧结主要取决于温度和烧结助剂,最大密度达到理论值的98％,借助SEM观察了表面及断口形貌,EDX作元素的半定量分析在1300℃试样表面发生了分解。     

Coloring effect of the organic hybrid of polyamide 6 and N,N′‐ethylene‐bis(tetrabromophthalimide)

Coloring study in organic hybrid of polyamide (PA6) and N,N′‐ethylene‐bis(tetrabromophthalimide) (EPT), where the chromophore was self‐assembled by hydrogen bonding formed between PA6 molecular chains and EPT compound, have been characterized by several techniques. CS930 double wavelength lamella scanner was employed to measure the change of color. The existence of hydrogen bonding in PA6/N‐N′‐ethylene‐bis (tetrabromophthalimide) (PA6EPT) was investigated with Fourier transform infrared (FTIR), the results of which were compared with that of PA6 with the same thermal history. FTIR spectra at room temperature revealed that there is essentially hydrogen bonding between PA6 and EPT. The crystallization behavior of PA6EPT affected by hydrogen bonding was studied by using FTIR. The temperature‐dependent behavior of both PA6 and PA6EPT was studied by temperature‐FTIR spectroscopy and differential scanning calorimetry (DSC). With temperature increasing, changes in sensitive, high‐resolution absorbance spectra are observed as dissolve‐volatilizing thin film. Temperature‐FTIR results showed that the hydrogen bonding in PA6EPT attenuated and dissociated considerably at a smaller rate than PA6, that is to say, hydrogen bonding in PA6EPT is more stable than that in PA6. DSC showed that the melting temperature of PA6EPT and PA6 are similar. However, the crystalline degree and crystalline temperature and melting enthalpy of PA6 and PA6EPT are different. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 594–600, 2007     

链霉亲和素-蛋白A融合蛋白基因在大肠杆菌中的表达

将合链霉亲和亲-蛋白A（Streptavidin－proteinA）融合蛋白基因的表达质粒pTSAPA导入大肠杆菌BL21（DE3），成功地表达了该融合蛋白，经SIJS－PAGE及免疫印迹等方法证实该蛋白既具有IgG的结合活性，又具生物素结合活性。     

Study of stability of high‐temperature polyimides using TG/MS technique

The oxidative stability of the carbon fiber‐reinforced composite of polyimide was examined, in real time, using the evolved gas analysis techniques. Off‐gas degradation products suggested the onset temperature for chain scissions to be fairly low at about 190–220°C. Based on the off‐gas products present and the trend of their release, the composite degradation mechanism appeared to be similar between 190 and 371°C, thereby marking 371°C to be the highest accelerated aging temperature for its long‐term lifetime prediction. Beyond 371°C, different degradation mechanisms would apply. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1219–1227, 2002     

聚乙烯转光棚膜的加工及应用研究

本文对聚乙烯转光棚膜的加工和光转换剂的作用、配比关系及物理性能进行了讨论。     

明胶中过氧化物的控制

在用药用明胶为主要原料生产药用空心胶囊的生产中,由于明胶中的过氧化物对胶囊中各种色素的颜色具有氧化褪色作用,胶囊产品放置时间过长,其颜色就会发生变化,加上药品自身安全性的要求等原因,故国内引进的外国胶囊生产线对明胶原料中的过氧化物含量的要求特别严格,要求明胶中不得检出过氧化物成分.尽管目前我国药典和轻工行业对药用明胶标准未作过氧化物含量的规定,相信很多生产药用空心胶囊的厂家对此项目都有内控标准,如本胶囊公司就规定,凡对购进的明胶均不得检出过氧化物成分,否则一律退货.笔者相信,不久的将业,药用明胶的标准修订肯定会增加过氧化物含量的规定.为此,明胶生产企业就必须在明胶生产中严格控制过氧化物的含量,使其达到客户的要求.     

三石─堇青石匣钵的研制

引入“三石”改善堇青石质匣钵性能,提高匣钵使用寿命。     

淤浆法HDPE装置低聚物不能结片原因探析

分析了淤浆法HDPE装置低聚物不能结片的原因,并提出了相应的工艺处理措施。     

Surface photografting polymerization of vinyl acetate,maleic anhydride,and their charge‐transfer complex. VI. Charge‐transfer complex (2)

The photografting copolymerization of a low‐density polyethylene/vinyl acetate (VAC)–maleic anhydride (MAH) binary monomer system was studied from the perspective of dynamics. The total conversion percentage (CP) and grafting conversion percentage (CG) were measured by gravimetry. On the basis of plots of CP and CG as functions of the polymerization time, the total polymerization rate (RP) and grafting polymerization rate (RG) were calculated. In addition, the apparent activation energy (E_a) and the reaction orders of the photografting polymerization under different reaction conditions, such as the total monomer concentration and the concentration of benzophenone (BP), were determined also. The results showed that, in comparison with the photografting polymerization of the two single monomers (VAC and MAH), RP and RG noticeably increased for the VAC–MAH binary monomer system. When the total monomer concentration was kept at 4M, the apparent E_a's of the three photografting polymerization systems were as follows: for VAC ([MAH]/[VAC] = 0/4), E_a's for the total polymerization and grafting polymerization were 41.00 and 43.90 kJ/mol, respectively; for MAH ([MAH]/[VAC] = 4/0, E_a's were 39.65 and 43.23 kJ/mol, respectively; and for the VAC–MAH binary monomer system, E_a's were 34.35 and 40.32 kJ/mol, respectively. These results suggested that the polymerization of the binary system occurred more readily than the other two. The reaction orders of RP with respect to the total monomer concentration of the monomers and the concentration of BP were 1.34 and 0.81, respectively. According to these investigations, it could be inferred that in the binary monomer system, both the free monomers and charge‐transfer complex took part in the polymerization; to the termination of the propagating chains, two possible pathways, unimolecular termination and bimolecular termination, coexisted in this binary monomer system. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 95: 910–915, 2005     

Al2O3／TiB2／SiCW陶瓷刀具加工镍基合金时的磨损机理研究

研究了Ａｌ２Ｏ３／ＴｉＢ２／ＳｉＣＷ陶瓷刀具加工Ｉｎｃｏｎｅｌ７１８镍基合金时的切削性能和磨损机理。结果表明；在低速切削条件下，Ａｌ２Ｏ３／ＴｉＢ２／ＳｉＣＷ和硬质合金刀具的抗后刀面磨损的能力相差不大；而在高速切削条件下，前者的抗后刀面磨能力远高于后者。