Chen’ s theorem in arithmetical progressions

LetN be a sufficiently large even integer and

顶空气相色谱法测定延生护宝液中甲醇残留量

本文用顶空气相色谱法，以ＧＤＸ－１０１为固定相，测定了延生护宝液中甲醇残留量，方法的回收率在８５．９％－１０１．６％之间，变异系数０．３％，最小检出量１．０ｍｇ／Ｌ。     

REDUCTION OF C=C DOUBLE BOND WITH BOROHYDRIDE EXCHANGE RESIN-TRANSITION METAL COMPOUND SYSTEMS

Borohydride exchange resin-transition metal(Co,Ni,Cu,)compoundsystems reduced C=C double to C-C single bond in ethanol.     

亲和标记-基质辅助激光解吸电离飞行时间质谱用于蛋白质相对定量方法的研究

将亲和标记技术和基质辅助激光解吸电离飞行时间串联质谱联用,建立了蛋白质相对定量方法,以牛血清白蛋白为实验对象,考察了该方法的准确度、重现性等指标;又以数种标准蛋白混合物为研究对象,考察了该方法的动态范围及相应的标准偏差,为实际生物样品中差异蛋白质分析奠定了基础。     

自动化流动注射停流动力学分析仪的研制及其性能测试

本文研制了一套自动化流动注射停流动力学分析仪，该仪器由苹果Ⅱ型微机通过１２位ＡＤ／ＤＡ卡，流动注射停流控制仪及用ＢＡＳＩＣ语言编制的软件控制泵的起动和停止，试样的输送和混合，数据采集和处理，结果显示和打印，通过以铁（Ⅲ）与硫氰酸盐的反应体系采用固定时间法和以钒（Ｖ）的胶束催化反庆体系采用安始速法的现场测试证明，该仪器具有结构简单，操作方便，恒温性能好，通用性强等特点。     

Amperometric biosensor for ethanol based on immobilization of alcohol dehydrogenase on a nickel hexacyanoferrate modified microband gold electrode

Alcohol dehydrogenase (ADH) has been immobilized on a nickel hexacyanoferrate modified microband gold electrode surface by a glutaraldehyde/bovine serum albumin (BSA) cross-linking procedure to provide a new amperometric sensor for the assay of ethanol. The resulting enzyme electrode exhibits excellent electrocatalysis for the oxidation of reduced nicotinamide-adenine dinucleotide (NADH). The amperometric determination is based on the electrochemical detection of NADH which is generated in the enzymatic reaction of ethanol with NAD(+) under catalysis of ADH. The influence of various experimental conditions was examined for the determination of the optimum analytical performance. The sensor responds rapidly to ethanol with a detection limit of (5.0 +/- 0.3) x 10(-7) mol 1(-1). The response current increases linearly with ethanol concentration up to 5 mmol 1(-1). The sensor remains relatively stable for about 1 week.     

ADSORPTION OF 2,4-DICHLOROBENZOXYACETIC ACID ONTO HYPERCROSSLINKED RESIN MODIFIED BY PHENOLIC HYDROXYL GROUP (AM-1)

INTRODUCTIONAdsorption has been considered to be the best available technology for removing organics from water in the USSafe Drinking Water Act[1]. Due to many drawbacks of activated carbon[2-7], the most widely used adsorbent,hypercrosslinked polymeric adsorbents developed by Tsyurupa and Davankov[8] have been increasingly viewedas an alternative to activated carbon for selective removal of specific organic substances from contaminatedwater[9-12], and series of researches have been do…     

共沉淀CuO-ZrO2复合氧化物分散态结构研究

用XRD、EXAFS、XPS表征了共沉淀法制备的CuO-ZrO2复合氧化物的分散态结构. 500 ℃焙烧的样品在一定组成范围内形成大体均匀的无定形态固溶体. CuO含量超过其在ZrO2中溶解度时，多余的CuO以CuO晶体形式存在；当ZrO2含量超过其在CuO中溶解度时，多余的ZrO2以四方相ZrO2晶体形式存在.焙烧温度达到800 ℃时，样品由单斜相ZrO2和CuO晶体组成.     

Determination of Organophosphorus Pesticides in Soil by MMSPD-GC-NPD and Confirmation by GC-MS

A novel method, modified matrix solid-phase dispersion (MMSPD), has been developed for quantitative analysis of organophosphorus pesticide residues in soil. It was based on matrix solid-phase dispersion (MSPD) and continuous liquid-solid extraction (continuous LSE), using Florisil as sorbent and dichloromethane as the recycling solvent. Two soils with different texture and physicochemical properties were studied to validate the method. The effect of residence time of pesticides in soil was also studied. MMSPD was compared with MSPD and continuous LSE respectively. Determination was carried out by gas chromatography with nitrogen-phosphorus detection (GC-NPD). The method gave recoveries ranging from 72–105% with relative standard deviations (RSDs) lower than 15% for the pesticides studied. The limits of detection (LODs) ranged from 0.1 to 0.6 ng g⁻¹. Two pesticide residues have been detected in real soil samples from Fujian, China, using MMSPD. The pesticides were confirmed by gas chromatography-mass spectrometry (GC-MS) in a selected-ion monitoring (SIM) mode. Revised: 4 and 9 April 2006