废水中铜银的分离和银的回收研究

废水中铜银的分离和银的回收研究黄秀山（四川三峡学院化学系万县６３４０００）关键词分解电压，还原电势，回收一、引言本实验采用电解还原的方法回收贵金属银。目前此法主要用于回收废水中的铬、汞等，对银的研究很少。曾有人进行过自然渗析还原法回收银的研究。用自然...     

Flaw-to-grain echo enhancement by split-spectrum processing

A split-spectrum processing technique for an ultrasonic flaw detection system has been developed which improves the flaw-to-grain echo ratio in large-grained materials. The enhancement is achieved by partitioning a wide-band received spectrum to obtain frequency shifted bands, which are then processed to suppress the grain echoes with respect to the flaw echo, using a novel signal minimization algorithm. Experimental data for titanium and stainless steel samples are presented which show superior flaw detection capabilities for the minimization algorithm with respect to frequency averaging techniques.     

相对论性核碰撞中φ介子增强

用强子和弦级联模型LUCIAE系统地研究了相对论性p+p和Pb+Pb碰撞中φ介子产生.在模型框架内实验测得的158AGeV/cPb+Pb碰撞中φ介子产额相对于同能量p+p碰撞的增强现象,依赖于弦发射胶子的集体效应和奇异夸克压低约化两机制,在一定程度内能得到解释.     

On the Integrability of Geodesic Flows of Submersion Metrics

Letters in Mathematical Physics - Suppose we are given a compact Riemannian manifold (Q,g) with a completely integrable geodesic flow. Let G be a compact connected Lie group acting freely on Q by...     

Cathodic synthesis of 2-amino-2-propene-1-ones electrolytical studies on vinylazides,VII

The cathodic preparation of enamino ketones from enazidoketones has been generalised to include heteroaromatic and aliphatic derivatives. Mechanistically the role of different sites of protonation, either on N¹ of the N₃-group or on carbonyl depending on electrolysis potential and acid strength, apparent by product distribution, is clarified. Aldehydic groups are preferentially reduced compared to the vinylazide part. Purely aliphatic azidoketones yield conjugated dienes under reductive acetylation, which might be useful for cycloaddition reactions.Die kathodische Synthese von Enaminoketonen aus ungesättigten Azidoketonen wurde auf heteroaromatisch substituierte und auf rein aliphatische Derivate übertragen. Zum Reduktionsmechanismus wurde der Einfluß verschiedener Stellen der Protonierung (am N¹ der N₃-Gruppe bzw. an der Carbonylgruppe), abhängig von Potential und Säurestärke, untersucht. Aldehydische Gruppen als weitere funktionelle Gruppen im Enazid werden leichter als die Vinylazide reduziert. Die rein aliphatischen Enazidoketone ergeben bei reduktiver Acylierung konjugierte Diene.

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Elektrolytische Untersuchungen an Vinylaziden, 7. Mitt.: Kathodische Synthese von 2-Amino-2-propen-1-onen

     

Determination of Metal Ions by High Performance Liquid Chromatography

The mixture of metal ions [Bi(III), Fe(III), Fe(II), Cu(II), Zn(II), Ni(II), Co(II), Pb(II), Cd(II), Mn(II)] were separated in the bonded-phase strong cation exchange column (Vydac-401 SA) and monitored at 540 nm after a postcolumn reaction with 4-(2-pyridylazo)-resorcinol (PAR). Citrate, tartrate, lactate and α-hydroxyisobutyrate buffer were used as eluent and it has been found that the elution order of some metal ions were changed with different eluents. The detection limits and the calibration curves of metal ions were also studied.     

Simulation methodology — An introduction for queueing theorists

Simulation is a widely used methodology for queueing systems. Its superficial simplicity hides a number of pitfalls which are not all as well known as they should be. In particular simulation experiments need careful design and analysis as well as good presentations of the results. Even the elements of simulation such as the generation of arrival and service times have a chequered history with major problems lying undiscovered for 20 years. On the other hand, good simulation practice can offer much more than is commonly realized.     

β-芳亚胺基醚还原裂解研究

刘铸晋等在测定钩吻素子1结构的工作中,发现1能被钠-醇还原裂解,亚胺基β位的醚键发生断裂,得到还原裂解产物——双氢钩吻醇2~([1])。其反应机理可能是一种自由基-阴离子反应,类似于苄基醚的还原断裂。如图式1所示: 反应的关键一步是一个单电子在化合物1中的碳氮双键上的加成,生成一个自由基-阴离子,接着发生β键的断裂及质子化。这种过程连续进行三次以后,就能获得还原裂解产物2。很明显,反应的决速一步是自由基的生成~([2])。为了进一步探讨这一反应的应用范围,我们合成了一系列具有各种亚胺体系的模型化合物,研究他们在钠-醇溶液中的反应情况。这些模型化合物是一系列的Schiff碱(见表1)。     

High-performance liquid chromatographic method for the simultaneous estimation of the key intermediates of duloxetine

A simple reversed-phase high-performance liquid chromatographic method employing C-18 column has been developed for simultaneous analysis of three intermediates in the synthesis of S-duloxetine, the antidepressant drug, viz., 2-acetyl thiophene (AT), N,N-dimethyl-3-keto-(2-thienyl)-propanamine (DKTP) and (S)-N,N-dimethyl-3-hydroxy-(2-thienyl)-propanamine (DHTP). Good separations were achieved by employing an isocratic system using acetonitrile and 0.05 M phosphate buffer (pH 7.0) containing 0.02% diethylamine. The detection was carried out at 241 nm. The method was validated for linearity, range, accuracy and precision. The developed method was applied for monitoring the progress of chemical synthesis of DKTP from AT followed by the biocatalytic reduction of DKTP to DHTP as the disappearance of the substrate and formation of the product can be monitored simultaneously by the present method.