双波长吸光光度法测定磷矿中氧化镁

以EGTA－Ba和SO4^2-为联合掩蔽体系，有效地消除因大量钙存在而产生的干扰。在PH10．2硼砂缓溶液中，镁与偶氮氯磷Ⅰ形成稳定络合物，用自制的双波长分光光度仪，在组合波长570nm和500nm下，用于磷矿中镁的测定。不需分离，方法简单，快速，结构满意。     

树脂对茶多酚与咖啡因的吸附分离

从低档绿茶末的水提取液中，利用离子交换，吸附树脂成功地分离出茶多酚与咖啡因，并详细考察了其交换与吸附性能。与其它方法相比，该树脂法具有产品收率高，成本低廉等特点。     

全氟辛基磺酸酸度函数H0的测定

It is reported in this paper that the acidity function H_0 of perfluorooctanesulfonic acid (POSA) is -12.11±0.03, which was measured first time by ~1H NMR method, in term of the α-H chemical shifts of the acid-ether systems, using 98% to 100% H_2SO_4 as reference standards. This method provides a new procedure for measuring the H_0 value of solid perfluoroalkanesulfonie acid C_nH_(2n+1)SO_3H(n>7).     

奋乃静和氟奋乃静的毛细管电泳柱端喷壁式安培检测

应用自组装毛细管电泳．安培检测装置，建立了同时分离检测抗精神病药奋乃静与氟奋乃静的新方法。在1050mV(vs．Ag／AgCl)检测电位下，奋乃静与氟奋乃静的检出限分别达0．060mg／L与0．075mg／L。在最佳检测条件下，两组分的响应电流与浓度之间有着良好的线性关系，线性范围为0．75～75mg／L。将方法用于药物片剂以及模拟尿样和血清样品中奋乃静和氟奋乃静的测定，结果令人满意。     

Indirect laser photoacoustic detection for trace samples on membranes

An indirect laser photoacoustic technique is described. The basic principle, the experimental set-up and the influencing factors are discussed in detail. This method was used to quantify phenylamine, arginine and methylene blue on membranes. The linear ranges of the calibration curve are up to two orders of magnitude. With 1 microliter of sample solution, the detection limits are 0.25, 1.52 and 0.14 pmol for phenylamine, arginine and methylene blue, respectively.     

可溶性聚硅酸铝铁的制备及其在废水处理中的应用

以赤泥为原料,制备了高效无机高分子絮凝剂——聚硅酸铝铁(PSAF),并将该絮凝剂用于处理工业废水．研究絮凝剂的使用效果与投加量、投加方式、pH值、搅拌条件及水样本身性能间的关系．     

Synthesis, crystal structure and spectroscopic properties of an unsymmetrical compound with carbazole and benzothiadiazole units

An unsymmetrical organic compound with carbazole (Cz) as donor and benzothiadiazole (BTD) as acceptor (D-π-A-π∗-D∗) was designed and synthesized via simple Heck reaction. The unique crystal structure of Cz-BTD-Cz∗ shows a ladder-like packing mode. A two molecule pair stacks parallelly with each other in each packing unit. In each cell, one Cz moiety is connected with BTD by vinylene bond in same plane. However, the other Cz group is connected to BTD by a one-end vinyl bond in almost perpendicular position to the coplanar part of the molecule. The shortest intermolecular plane distance is 3.48 ± 0.1 Å. The photophysical properties of Cz-BTD-Cz∗ in solution and in bulky crystalline powder state were studied. In bulk crystalline powder state, it has a red-shifted emission band peaked at 609 nm relative to that in solution, and the FWHM was reduced to only 58 nm. Electrochemical properties were also investigated.     

Heterogeneous catalytic aerobic oxidation behavior of Co–Na heterodinuclear polymeric complex of Salen-crown ether

A new kind of Co–Na heterodinuclear polymer complex based on Salen Schiff base and crown ether has been successfully prepared by condensation polymerization. Its catalytic behavior for aerobic oxidation of cyclohexene, alkylbenzenes and linear aliphatic olefins was studied in the absence of any solvents or reducing agents under mild conditions. The oxidation of cyclohexene catalyzed by the above catalyst proved to be a simple and efficient method for obtaining 2-cyclohexen-1-one (CO) and 2-cyclohexen-ol (OH) in a high selectivity. Kinetics of the oxidation was also investigated. The results showed that the aerobic oxidation of cyclohexene catalyzed by Salen-crown ether heterodinuclear polymer complex follows a radical chain aerobic oxidation mechanism. This oxidation system is also efficient in the oxidation of alkylbenzenes and linear aliphatic olefins, which afforded corresponding benzylic oxidation products and epoxides, respectively.     

MODIFICATION OF TRANSITION METAL CATIONS TO POLYMER-STABILIZED PLATINUM COLLOIDAL CLUSTERS IN ENANTIOSELECTIVE HYDROGENATION OF METHYL PYRUVATE

Modification of transition metal cations to polymer-stabilized Pt colloidal clusters modified with cinchonidine was studied in enantioselective hydrogenation of methyl pyruvate. Compared to the enantiomeric excess (e.e.) value (71.4%) obtained without the presence of metal cations, obvious e.e. enhancement (up to 82.5%) was resulted from the addition of Zn^2 but with a certain decrease in activity. The reaction parameters in the presence of Zn^2 were also studied. It was found that the Pt colloidal catalysts in the presence of metal cations performed very differently from that in the absence of metal cations.