液膜法处理含氟废水

为了防止含氟废水的污染,人们研究了多种除氟方法,液膜技术是一项新的分离工艺,它操作简单,试剂用量少,有机相可重复利用。本文利用伯胺作迁移载体处理高含量的含氟废水,分离效率较好。 伯胺N_(1923)(简写RNH_2)为流动载体,上胺N_(205)(上海石油化工厂)为表面活性剂,煤油为溶剂。将内相CaCl_2,溶液与油相(含N_(1923)、N_(205)和煤油)按一定体积比例混合,高速搅拌,制成W/O     

KZnF3：Eu^3＋单晶生长及光谱特性

利用Ｂｒｉｄｇｍａｎ－Ｓｔｏｃｋｂａｒｇｅｒ方法在氩气气氛下生长出ＫＺｎＦ３：Ｅｕ＾３＋单晶，测定了晶体的激发光谱、荧光发射光谱和ＥＳＲ谱，讨论了Ｅｕ离子的取代格位。     

AN INVESTIGATION ON THE ab initio CALCULATION OF INTERMOLECULAR INTERACTION——NON-BONDED INTERACTION IN THE HYDROGEN BOND COMPLEX (HF)_2

An ab initio calculation of the hydrogen bond complex (HF)_2 is given with the 6-311 G~(**) basis set, according to which the potential surface around the balance point of the distancès and the orientations between two HF molecules is obtained. The atomic charges in the system are calculated with the PD/LSF method (potential-derived/least-square-fitting method) and then an analysis of the hydrogen bond interaction between two HF molecules is given with the (exp-6-1) potential function, by means of which it is shown that the main interaction between them is not an electro-static but a charge transfer one. The potential curve between two HF molecules is like a Morse function.     

合成CFC-12替代物HFC-134a的CrF3/AlF3催化剂的研究

考察了不同反应条件下ＨＣＦＣ－１３３ａ与ＨＦ在ＣｒＦ３／ＡｌＦ３催化剂作用下生成ＨＦＣ－１３４ａ的反应性能。需用ＧＣ－ＦＴＩＲ方法鉴定了产物的组成，探讨了副产物形成的原因，并进行了催化剂的稳定性试验。结果表明在ＨＦ／ＨＣＦＣ－１３３ａ流量比为１０和３５０℃和条件下，得到了较高的转化率和选择性。     

Novelties of solid-liquid phase transfer catalysed synthesis of p-toluenesulfonyl fluoride from p-toluenesulfonyl chloride

Organic sulfonyl fluorides are of interest owing to their insecticidal, germicidal and enzyme inhibitory properties. In the current work, synthesis of p-toluenesufonyl fluoride was accomplished by reacting p-toluenesulfonyl chloride with solid potassium fluoride using PEG-400 as a catalyst under solid-liquid phase transfer catalysis (S-L PTC) at 30 °C. p-Toluenesulfonyl fluoride is used as peroxygen bleach activator. It also finds use in the treatment of Alzheimer's disease. The mechanism is based on homogeneous solubilization of solid. PEG forms a complex with metal cation which associates with the nucleophile and it participates in SN₂ type reactions. The reaction is intrinsically kinetically controlled. A complete theoretical analysis is done to determine both the rate constant and equilibrium constant from the same set of data. The activation energy and Gibbs free energy are also calculated.     

Die Kristallstruktur von Na2NiAlF7—ein Beitrag zum Problem der wahren Raumgruppe orthorhombischer Weberite

The Crystal Structure of Na₂NiAlF₇ — a Contribution to the Problem of the True Space Group of Orthorhombic Weberites The X-ray single crystal structure determination of the orthorhombic weberite Na₂NiAlF₇ (a = 707.4(2), b = 1003.8(2), c = 731.5(1) pm; Z = 4) was performed in space group Imma, after all reflections hk0 with h(k) = 2n + 1 could be eliminated, as they proved simulated by Renninger effect and/or λ/2 reflections. The alternative space groups Imm2 resp. I2₁2₁2₁ of former weberite structure determinations thus became obsolete. The refinement using 880 independent reflections ended at wR = 0.0232. The resulting average distances within the framework of octahedra are Ni? F = 197.3, Al? F = 180.4 pm.     

Organic Reactions in Ionic Liquids： An Efficient Method for the Synthesis of Phenacyl Esters by Reaction of Carboxylic Acids with α-Bromoacetophenone Promoted by Potassium Fluoride

An efficient method is reported for the synthesis of phenacyl esters by reaction of carboxylic acids with a-bromoacetophenone promoted by potassium fluoride in ionic liquid [Bmim]PF6, the yield of the reaction is almost quantitative and the products are essentially pure.     

Tetrabutylammonium cyanide catalyzed diasteroselective cyanosilylation of chiral α-hydroxyketones

Tetrabutylammonium cyanide has been used as non-metallic catalyst for the diastereoselective cyanosilylation of α-hydroxyketones derived from the chiral pool. This affords α-substituted-α,β-dihydroxynitriles with high levels of asymmetric induction.     

PIXE法分析共聚物中痕量氯

四氟乙烯和全氟4-甲基-3,6-二氧杂-△~7辛基磺酰氟在溶剂氟里昂-113(F-113)中进行自由基引发聚合反应时,共聚物(T-O)是否有链转移,可以通过测定所得共聚物中的含氯量来得以证实。我们首次应用质子X萤光分析法(PIXE)进行分析。结果表明,共聚物中含氯量小于1ppm,F-113溶剂并未发生链转移。同时,我们测定了已证明有F-113参与链转移反应的F_(40)试样,含氯量高达700ppm。