Synthesis of Titanate Derivatives Using Ion-Exchange Reaction

Two types of titanate derivatives, layered hydrous titanium dioxide (H₂Ti₄O₉· n H₂O) and potassium octatitanate (K₂Ti₈O₁₇) with a tunnellike structure, were synthesized using an ion-exchange reaction. Fibrous potassium tetratitanate (K₂Ti₄O₉· n H₂O) was prepared by calcination of a mixture of K₂CO₃ and TiO₂ with a molar ratio of 2.8 at 1050°C for 3 h, followed by boiling-water treatment of the calcined products for 10 h. The material then was transformed to layered H₂Ti₄O₉· n H₂O through an exchange of K⁺ ions with H⁺ ions using HCl. K₂Ti₈O₁₇ was formed by a thermal treatment of KHTi₄O₉· n H₂O. Pure KHTi₄O₉· n H₂O phase was effectively produced by a treatment of K₂Ti₄O₉ with 0.005 M HCl solution for 30 min. Thermal treatment at 250°–500°C for 3 h resulted in formation of only K₂Ti₈O₁₇.     

离子交换法提取井冈霉素的研究

本文就不同树脂对井冈霉素的吸附性能及其影响因素作了研究，得到了离子交换法提取井冈霉素较佳工艺条件，从而获得了高单位效价的井冈霉素粉剂。     

Correlation between Grain Size and Thermal Expansion for Aluminum Titanate Materials

Al₂TiO₅ materials were sintered under different conditions to produce different grain sizes. The resultant microcracked materials exhibited a range of bulk thermal expansions which showed a strong correlation with average grain size. An Al₂TiO₅ average grain size of 3 to 4 μm was the minimum at which the size and population of microcracks effectively reduced the apparent thermal expansion of the polycrystalline material. Further increases in grain size resulted in a rapid drop in the bulk thermal expansion, followed by diminishing decreases with further increases in grain size. Small amounts of phase stabilizers (<2.1 wt% MgO or Fe₂O₃) or limited mullite additions in mullite—aluminum titanate composites had no significant effect on this correlation.     

硼吸附用聚丙纤维接枝苯乙烯离子交换纤维

研制了一种应用于硼吸附的苯乙烯系离子交换纤维,该离子交换纤维是采用市售聚丙烯纤维接枝苯乙烯的复合纤维产品为骨架,通过氯甲基化,然后导入N-甲基葡萄糖胺基进行氨化反应,从而得到具有硼选择性吸附的离子交换纤维。这种选择性离子交换纤维不受大量共存盐类的影响,能只对硼酸选择捕捉,同时具有较高的比表面积,可代替颗粒状离子交换树脂用于硼的吸附,因此具有很高的实用价值。     

Flextensional Barium Strontium Titanate Actuators

This paper describes the performance of the cymbal flextensional transducer using Dy-doped barium strontium titanate (BST) as the driver material. BST was first characterized for its dielectric and loss behavior as a function of temperature and electrical bias field. With no electrical bias, the transition temperature was measured to be near 20°C and have a dielectric constant >20 000. The strain of a BST disk was then measured and compared with other ceramics. At room temperature the strain and average effective piezoelectric d ₃₃ of this non-lead composition was slightly larger than Navy type I lead zirconate titanate (PZT-4) ceramic. The strain/field behavior was also measured as a function of temperature. Cymbal capped BST ceramic was found to have an amplified displacement of 28×, also very similar to type I ceramic. The stiffness of BST was found to be tunable by dc voltage and 2 to 3 times larger than that of PZT. This material has promise for applications in actuators and transducers with large generative force.     

离子交换树脂在有机溶剂中的脱盐行为研究

The desalting property of ion-exchange resins in organic solvent is reported by using potassium acetate as a model compound. The experimental results show that the solvability of the solvent, stirring speed, and temperature are the factors which influence the ion-exchange rate. The increase of solvability, stirring speed and temperature will speed up the ion-exchange process.     

The Desalting Property of Ion-Exchange Resins in Organic Solvent

The desalting property of ion-exchange resins in organic solvent is reported by using potassium acetate as a model compound. The experimental results show that the solvability of the solvent stirring speed, and temperature are the factors which influence the ion-exchange rate. The increase of solvability, stirring speed and temperature will speed up the ion-exchange process.     

离子交换法回收锰矿废水中锰的研究

选用XPD850树脂对湖北蒙特锰业有限公司的锰矿废水所含锰进行回收,研究了温度、时间及pH对吸附性能的影响,解吸剂种类及解吸条件,并对其经济性进行了评价。研究表明:以吸附流出液的Mn2+浓度小于2mg/L为穿漏标准,XPD850树脂对锰矿废水的吸附能力可达到25倍以上的树脂体积,动态饱和交换容量约87mg/mL。     

Properties of Aqueous Bismuth Titanate Suspensions Stabilized by Acrylic Acid/Acrylic Ester Copolymer

The properties of an aqueous Bi₄Ti₃O₁₂ suspension stabilized by an acrylic acid/acrylic ester copolymer have been investigated. The adsorption of a copolymer on Bi₄Ti₃O₁₂ surface resulted in a dramatic increase in the absolute zeta potential at pH 3–11. Coincidentally, the rheological property of the suspension was significantly improved. The adsorption quantity increased with increasing copolymer concentration at first, then decreased as the copolymer concentration was beyond 1.5 wt%. The viscosity varied in a complicated manner with copolymer concentration, due to the variations in the adsorption quantity and adsorption configuration of the copolymer molecules on Bi₄Ti₃O₁₂ particle surface. High-quality tapes were prepared through tape casting.     

超凝胶离子交换树脂研究初探

介绍了超凝胶离子交换树脂研究概况及实验方案,并分析了与各种因素的关系,提供了研究的思路.     

Generalized Titanate Ceramic Waste Form for Advanced Purex Reprocessing

Alternative dissolution processes for spent nuclear fuel lead to highly active waste streams rich in zirconium, iron, chromium, and nickel at levels that vary with fuel assembly design. A titanate ceramic phase assemblage has been developed with the flexibility to accommodate these variations in waste stream composition. Waste loadings range from 42 to 50 wt%. Leach rates are comparable to those from Synroc C.     

Electric-Field Effects on Sintering and Reaction to Form Aluminum Titanate from Binary Alumina–Titania Sol–Gel Powders

The field-activated sintering technique (FAST) was applied to simultaneously sinter and react sol–gel amorphous powders to form Al₂TiO₅. Densities close to theoretical and conversion to Al₂TiO₅ (to 92.5%) have been achieved using FAST at 1050°–1200°C for 10 min. Conventional sintering of the same powders at 1300°C for 2 h resulted in 88.9% Al₂TiO₅ and ∼75% of theoretical density. The enhanced sintering and compound formation using FAST have been explained by the synergistic effects of precursor reactivity, nanosized powders, and electric-field effects.     

离子交换树脂对咖啡因溶液提浓性能的研究

选用不同型号阳离子交换树脂和洗脱剂,对1%咖啡因溶液交换、洗脱过程进行研究。结果表明:相比于724、D-113、D-151树脂,732树脂交换处理量达10BV,洗脱速度快,单次洗脱浓度可达3.82%;80℃水更适合作为洗脱剂;经过3次叠加交换、洗脱后,1%咖啡因溶液提浓到7.39%,可为工业生产中结晶母液回收咖啡因过程提供参考。     

蛋白质在离子交换吸附剂颗粒中的扩散系数

采用以化学势梯度作为扩散推动力的Maxwell-Stephan扩散方程（MS方程）,结合平行扩散模型,对阴离子吸附剂Q-SepharoseFF吸附牛血清白蛋白（BSA）的动态试验数据进行了模拟,拟舍得到了BSA的表面扩散和孔扩散系数。研究表明表面扩散系数随pH降低、盐浓度增加而增大;孔扩散系数随pH增加、盐浓度降低而增加,随蛋白质初始浓度增加而减小。在表面扩散不容忽视且为非线性吸附的条件下采用Fick定律时得到的表面扩散系数是蛋白质浓度的函数,且大于根据MS方程得到的表面扩散系数。     

Nonepitaxial Orientation in Sol–Gel Bismuth Titanate Films

Control over crystallographic orientation in ceramic thin films is important for highly anisotropic structures. Layered perovskites, like Bi₄Ti₃O₁₂, have interesting properties associated with their ferroelectric nature, which may be fully exploited only when films are highly textured. Textured films of this titanate were fabricated via a sol–gel technique without using epitaxial growth. Orientation in the film is confirmed by XRD and SEM, and supported by refractive index and dielectric measurements. In an attempt to explain the orienting effect, light scattering experiments were conducted to yield information about the molecular size, shape, and conformation of macromolecules as the sol–gel solution ages and condensation reactions proceed. These experiments clearly show an increase in the size of molecular clusters with time. We believe that it is the organization of these large clusters during spin coating, and the relationship of the backbone chemistry to the crystal structure of Bi₄Ti₃O₁₂, that are responsible for the observed orientation.     

Bismuth Titanate from Mechanical Activation of a Chemically Coprecipitated Precursor

Most of the chemistry-based preparation routes for bismuth titanate (BIT) involve calcination at elevated temperatures in order to realize precursor-to-ceramic conversion. In a completely different approach using an amorphous BIT hydroxide precursor, nanocrystalline particles of layered perovskite BIT are synthesized by mechanical activation, skipping the detrimental crystallite coarsening and particle aggregation encountered at high temperatures. Mechanical activation leads to nucleation and steady growth of BIT crystallites in the amorphous precursor matrix, while Bi₂O₃ is involved as an intermediate transitional phase. The activation-derived BIT particles demonstrate a rounded morphology of ∼50 nm in size. This is in contrast to the BIT derived from calcination of the coprecipitated precursor at 600°C that is dominated by coarsened platelike particles. The former is sintered to a density of >95% theoretical at 875°C for 2 h, leading to a dielectric constant of ∼1260 when measured at 1 MHz and the Curie temperature of 646°C.     

Crystallographic Texture Development in Bismuth Sodium Titanate Prepared by Reactive-Templated Grain Growth Method

Bi_0.5Na_0.5TiO₃ (BNT) and 0.94Bi_0.5Na_0.5TiO₃·0.06BaTiO₃ (BNT–BT) bulk ceramics with extensive 〈100〉 texture were prepared by the reactive-templated grain growth method, using platelike Bi₄Ti₃O₁₂ (BIT) particles as templates for BNT. Calcined compacts were composed of matrix grains with random orientation and 〈100〉-oriented grains transformed from aligned BIT particles, and the texture developed by the growth of oriented grains during sintering. Ceramics with extensive texture were obtained by using the starting mixture containing the maximum concentration of platelike BIT to form the maximum volume fraction of oriented grains.     

固相法烧结温度对钛酸钡陶瓷介电性能的影响

研究了固相法烧结温度对钛酸钡陶瓷介电性能的影响.采用固相法在不同温度下烧结钛酸钡陶瓷.结果表明,不同烧结温度对钛酸钡陶瓷晶体结构、微观形貌、介电常数、介电损耗、居里温度等都会产生不同的作用效果.钛酸钡陶瓷只有在最佳烧结温度附近才具有最好的结构和性能,烧结温度过低会使烧结过程不充分,引起过多的点缺陷;而过高的烧结温度也会由于过烧现象的存在而使晶粒与晶界间相互作用出现异常,两种情况都会导致钛酸钡陶瓷介电性能的劣化.     

Hydrothermal Synthesis of Bismuth Titanate Powders

Bismuth titanate was synthesized under hydrothermal conditions from an amorphous bismuth–titanium precursor gel. The gel was formed by mixing a bismuth acetate complex with titanium butoxide and then adding the solution dropwise into 6 M NaOH. The resulting gel suspension was reacted under hydrothermal conditions at temperatures ranging from 160° to 200°C to form crystalline bismuth titanate. The gel crystallization kinetics increased with temperature, which resulted in 100% crystalline bismuth titanate in 5 h at 200°C. Wavelength-dispersive spectroscopy data indicated that sodium was incorporated into bismuth titanate during processing, and X-ray diffractometry suggested that the powder was composed of the Bi₅Ti₄O₁₅ phase. Transmission electron microscopy micrographs showed that the gel particles decomposed to 100–200 nm crystalline bismuth titanate particles during hydrothermal processing.