溶剂对反胶束法合成CdS纳米粒子粒径的影响

以磺基琥珀酸二辛酯钠盐(AOT)为保护剂,利用反胶束法在不同烷烃溶液中合成了CdS纳米粒子.采用紫外-可见光谱、透射电子显微镜、荧光光谱法对其进行表征.研究表明:在不同烷烃溶液中合成的CdS纳米粒子,其粒子大小和荧光强度都随溶剂而改变.     

碳酸盐前驱物制备Y2O3超细粉及透明陶瓷

以Y(NO3)3和NH4HCO3为原料,通过向Y(NO3)3溶液中滴加NH4HCO3的方式制备了化学组成为Y2(CO3)3·2H2O的先驱沉淀物。研究了先驱沉淀物煅烧过程中的物相变化。先驱沉淀物1100℃煅烧4h后得到了平均粒径为60nm的无团聚Y2O3超细粉体。所得粉体不添加任何添加剂,在1700℃下真空烧结4h得到了透明Y2O3陶瓷。     

Kinetic spectrophotometric determination of trace manganese (II) with dahlia violet in nonionic microemulsion medium

A new catalytic kinetic spectrophotometric method has been developed for the determination of trace amount of manganese (II) in nonionic microemulsion medium. The method is based on the catalytic effect of manganese (II) on the oxidation of dahlia violet by potassium periodate with nitrilotriacetic acid as an activitor in the presence of nonionic microemulsion. Under the optimum conditions, the calibration graph is linear in the range of 0.0004-0.0056 μg ml⁻¹ of manganese (II) at 580 nm. The detection limit achieved is 3.75×10⁻⁵ μg ml⁻¹. Manganese (II) in foodstuff samples was determined with satisfactory results.     

离子交换-双氧水氧化法制备纳米CeO2晶体

以99.995% Ce(NO₃)₃和强碱性阴离子交换树脂为原料，采用离子交换-双氧水氧化法合成制备出纳米CeO₂晶体。并就离子交换反应中的Ce³⁺浓度、树脂加入速度和离子交换温度及H₂O₂加入速度等条件对CeO₂粒径的影响进行了探讨，得出了离子交换-双氧水氧化法制备纳米CeO₂晶体的最佳工艺条件。FTIR、TEM分析表明，离子交换法无需对合成的Ce(OH)₃溶胶进行洗涤即可去除NO₃^-、CO₃^2-等阴离子杂质，并用H₂O₂将该溶胶氧化，经真空干燥可制得粒径分布均匀，平均晶粒尺寸约3 nm，高纯度的CeO₂粉体。     

食用菌中Cu、Mn、Fe、Zn含量的测定

采用火焰原子吸收法测定洛阳地区11种栽培食用菌中Cu、Mn、Fe、Zn的含量,旨在指导人们调节膳食结构,同时也为食用菌产品的开发利用和深加工提供科学依据。测定结果表明,食用菌中含有丰富的微量元素,是不可多得的营养补品,也是值得开发的保健食品,大量种植将会有更加广阔的市场前景。     

Synthesis and Cytotoxic Activity of 4-Substituted 3-Cyano-6,6-dimethyl-5,6-dihydro-2-pyranones

The respective 4-(arylvinyl)lactones and compounds of the Michael adduct type were synthesized by the condensation of substituted benzaldehydes with 3-cyano-4,6,6-trimethyl-5,6-dihydro-2-pyranone in the presence of catalytic amounts of sodium hydroxide. It was shown by the semiempirical AM1 method that the indicated products can be formed through one and the same intermediate compound. Some of the synthesized phenylvinyl-5,6-dihydro-2-pyranones have a cytotoxic effect, and this corresponds to the prognosis of the OREX expert system.     

Et2NH2[Nd(S2CNEt2)4]的晶体结构和生成反应焓变

在干燥氮气气氛下,以无水乙醇为溶剂,制备了低水合氯化钕与二乙氨基荒酸二乙铵(D-DDC)配合物,确定其组成为Et2NH2[Nd(S2CNEt2)4].单晶结构分析表明,配合物中4个二乙氨基荒酸根各通过2个硫原子与钕离子成键形成八配位十二面体阴离子,并与二乙铵阳离子形成缔合型分子.晶体属单斜晶系,空间群P21/n,a=1.37517(14)nm,b=2.1146(2)nm,c=1.44641(15)nm,β=102.028(2)°,Z=4.用微量热法测定了298.15K下水合氯化钕和D-DDC在无水乙醇中的溶解焓及二乙氨基荒酸钕液相生成反应焓变分别为(-17.89±0.096),(50.280±0.151)和(-10.116±0.065)kJ/mol,求得固相生成反应焓变.     

Thermal transformations in systems based on zeolites Y,X, and A containing zinc and sodium nitrates

Thermal transformations in systems formed by interaction of Zn and Na nitrates with Y, X, and A zeolites were studied by TG—DTA technique. Temperature regions of existence of adsorbed water, water of crystallization, and decomposition of NO₃ ^– anion were determined. These intervals depend on the composition, structure, method of preparation, and pre-treatment conditions of zeolite systems. The extent of NO₃ ^– decomposition depends not only on the zinc and sodium content but also on the presence of ammonia involved in NO₃ ^– reduction. The zeolite matrix strongly stabilizes the occluded NO₃ ^– anions. A portion of zinc oxide formed by zinc nitrate decomposition is probably localized inside the zeolite cavities as the [Zn—O—(ZnO) _n —Zn]²⁺ particles. The latter compensate charges of the isolated [AlO₄]^– tetrahedra.     

头孢类抗生素定量结构-活性关系的密度泛函研究

用量子化学密度泛函方法B3LYP对9种头孢类抗生素的电子结构进行了理论计算, 并对它们进行了定量构效关系研究. 建立了头孢类抗生素分子的结构-活性数学模型: 头孢类抗生素的抑菌活性与QC8, QC7以及偶极距(Dipole)呈正相关关系.     

Theoretical Study on the Reaction Mechanism of Ketene CH2CO with Isocyanate NCO Radical

The bimolecular single collision reaction potential energy surface of an isocyanate NCO radical with a ketene CH2CO molecule was investigated by means of B3LYP and QCISD（T） methods. The computed results indicate that two possible reaction channels exist on the surface. One is an addition-elimination reaction process, in which the CH2CO molecule is attacked by the nitrogen atom at its methylene carbon atom to lead to the formation of the intermediate OCNCH2CO followed by a C-C rupture channel to the products CH2NCO＋CO. The other is a direct hydrogen abstraction channel from CHzCO by the NCO radical to afford the products HCCO＋HNCO. Because of a higher barrier in the hydrogen abstraction reaction than in the addition-elimination reaction, the direct hydrogen abstraction pathway can only be considered as a secondary reaction channel in the reaction kinetics of NCO＋ CH2CO. The predicted results are in good agreement with previous experimental and theoretical investigations.