萃取预分离法分离富铕中钇矿新工艺

采用一种新的串级萃取方式--萃取预分离法分离富铕中钇矿的新工艺.原料首先流入十几的三出口预先粗分离工艺,其萃余液La～Gd(TbDy)直接流入Nd/Sm工艺;中间出口流入(Gd)Tb～HoY(Er)Gd～Dy/Ho～LuY细分离工艺;出口负载有机相(Ho)Er～LuY流入Gd～Dy/Ho～LuY的洗涤段.结果表明,新工艺的粗分离工艺将占原料约70%的La～Gd(TbDy)预分离掉,使流入Gd～Dy/Ho～LuY工艺的稀土量减少约70%;由于Gd～Dy/Ho～LuY分组的萃余液GdTbDy含Ho2O3小于0.03%,省去原工艺的GdTbDy/HoY分离;新工艺的处理能力提高30%,酸碱消耗减少20%以上,贵重稀土元素Eu和Tb的存槽量大大减少.     

An improved light attenuation technique for measuring large interfacial areas

A laser-based light attenuation technique was successfully used to measure interfacial areas as high as 5832 m²/m³ and Sauter mean bubble diameter varying between 50 and 5600 μm. Good agreement between this approach and the photographic technique was obtained particularly at low gas holdups.     

高效液相色谱法测定卷柏中的穗花杉双黄酮

用反相高效液相色谱法测定卷柏提取物中的穗花杉双黄酮。结果表明：穗花杉双黄酮在质量浓度为41.2mg／L～206mg／L时，峰面积Y与其质量浓度X的线性关系良好，回归方程为Y=547．028X 15．4895(r=0.9999)，最低检测限为2．0μg/L；穗花杉双黄酮的平均回收率为99．42％(n=3)，相对标准偏差RSD为0．79％；连续进样、日内进样和日间进样所得检测结果的RSD分别为0．12％、0．11％和0．11％。     

内陆核电厂放射性废液中硼酸的反渗透分离实验研究

建设内陆核电是我国经济社会发展的必然需求,但由于内陆核电自然环境和社会环境的特殊性,必须更进一步考虑排放对环境和公众的安全影响,对放射性废液进行深化处理,在解控排放的基础上进一步降低排放水平。本文在内陆AP1000机组已实施的放射性废液处理系统改进的基础上,开展了放射性废液深化处理研究,通过大量实验考察了不同进水pH值、硼浓度、含盐量、水温等水质条件和不同工作压力、回收率等运行条件下反渗透装置对硼酸的去除性能和对模拟放射性核素的截留能力。结果表明,通过控制适当的工艺条件,可以去除废液中80%以上的硼酸,同时保持很好的核素去除效果,达到进一步降低排放水平的目的。研究成果可为内陆核电厂放射性废液处理系统深化处理工程应用提供有力的技术支撑,并为后续内陆核电放射性废液深化处理提供参考。     

纤维素衍生物液晶相转变和织态结构

本文综述了纤维素衍生物液晶态相转变和织态结构。描述了纤维素衍生物从各向同性态向液晶态的转变过程和液晶态的织构特征。讨论了溶液浓度和温度对液晶相织构的影响。探讨了各种因素,如溶剂、取代基含量、外加力场和外加磁场等对液晶相的形成及织态结构的影响。     

Gas hold-up in non-newtonian solutions in a bubble column with internals

Bubble characteristics and gas hold-up were studied in a two phase (air-aqueous CMC solution) bubble column provided with helical coils and straight tubes as internals. The effects of superficial gas velocity, rheological properties, and volume fraction covered by the internals, on gas hold-up were studied. Hold-up values determined directly and by simultaneous pressure drop measurements matched well. Enhancement of gas hold-up values up to 55 per cent was achieved in systems using internals. The gas hold-up results were also compared with the values obtained from correlations reported in the literature.     

反相高效液相色谱法测定meso-四苯基卟啉钴的纯度

采用反相高效液相色谱法测定合成meso-四苯基卟啉钴的纯度;以甲醇乙腈二氯甲烷(体积比为55∶35∶10)为流动相,ShimpackCLCODS柱(150mm×6.0mmi.d,5μm)为分离柱,流速为1.5mL/min,检测波长420nm;meso四苯基卟啉钴的测定在1.0～10μg/mL时线性关系良好(相关系数r=0.9993),加标回收率为97.03%～101.42%,重复进样的相对标准偏差RSD为0.64%～2.92%(n=5)。方法的准确度高,精密度好,实际应用效果好。     

莫达非尼的绿色化学合成

采用[bm im]BF4离子液体作为反应溶剂,以二苯甲硫醇为原料,经醚化、氨解、氧化得到新型提神醒脑药物莫达非尼。讨论了不同的氯乙酸酯和反应温度对醚化反应收率的影响,讨论了不同的二苯甲硫乙酸酯对氨解反应收率的影响,及离子液体的回收使用。研究表明,采用氯乙酸甲酯作为醚化试剂,反应时间4 h,反应温度100℃,二苯甲硫醇∶氯乙酸甲酯=1∶1.5(摩尔比),室温下氨解反应20 h,二苯甲硫乙酰胺收率76%;采用过氧化氢作为氧化试剂,反应时间3 h,反应温度60℃,过氧化氢∶二苯甲硫乙酰胺=1∶1(摩尔比),莫达非尼收率79%,反应总收率可达48%。     

SEPARATION AND ENRICHMENT OF WEAK ORGANIC ACIDS OR BASES BY IMMOBILIZED LIQUID MEMBRANES

A new and effective liquid membrane process to achieve both separation and enrichment simultaneously of weak organic acids or bases was developed. The process utilizes effectively the difference in the apparent partition coefficient of the constituent species between the aqueous and organic phases, and uses the change of the apparent partition coefficients with the hydrogen ion concentration of the aqueous phase. For such a fundamental model apparatus as a diaphragm diffusion cell being operated batch wise, the effects of pK value of solutes, permeability of solutes through the membrane, volume ratio of liquids in two aqueous phases, and pH value of aqueous phase on enrichment factor and selectivity for the solute to be concentrated were discussed analytically. Separation and enrichment were demonstrated using aqueous mixed solutions of fumaric acid and L-malic acid. The results were in good agreement with the theoretical predictions.