高效液相色谱-电感耦合等离子体发射光谱联用的瞬时信号采集和处理软件及实际应用

本文对高效液相色谱-电感耦合等离子体原子发射光谱联用技术进行了研究.对所用ICAP-9000型等离子体原子发射光谱仪的控制采样程序进行了部分修改,采集的数据通过异步串行通讯方式由AppleⅡ微机传送至IBM PC286机进行处理。发展的瞬时信号采集程序能满足HPLC的检测要求,并将这一联用技术成功的用于砷的形态分析.     

Visual recognition of melamine in milk via selective metallo-hydrogel formation

A novel protocol allowing convenient and highly selective visual recognition of melamine in raw milk via selective metallo-hydrogel formation at a concentration as low as 10 ppm without any tedious pretreatment has been developed.     

改进型甲醇合成催化剂NC208的催化特性

采用ＴＰＤ、ＸＲＤ、ＢＥＴ和Ｈ２Ｓ中毒试验等方法，对比研究三组份（Ｃｕ－Ｚｎ－Ａｌ）甲醇合成催化剂Ｃ２０７和添加少量金属氧化物的改进型催化剂ＮＣ２０８．结果表明，工作态ＮＣ２０８催化剂表面Ｃｕ＋／Ｃｕ０的比值和价态稳定性大于Ｃ２０７．     

Optical detection of triggered atherosclerotic plaque disruption by fluorescence emission analysis

Fluorescence emission analysis (FEA) has proven to be very sensitive for the detection of elastin, collagen and lipids, which are recognized as the major sources of autofluorescence in vascular tissues. FEA has also been reported to detect venous thromboemboli. In this paper we have tested the hypothesis that FEA can reproducibly detect in vivo and in vitro triggered plaque disruption and thrombosis in a rabbit model. Fluorescence emission (FE) spectra, recorded in vivo, detected Russell's viper venom (RVV)-induced transformation of atherosclerotic plaque. FE intensity at 410-490 nm 4 weeks after angioplasty was significantly lower (P < 0.0033 by analysis of variance) in RVV-treated rabbits when compared to control animals with stable plaque. FE spectral profile analyses also demonstrated a significant change in curve shape as demonstrated by polynomial regression analysis (R2 from 0.980 to 0.997). We have also demonstrated an excellent correlation between changes in FE intensity and the structural characteristics detected at different stages of "unstable atherosclerotic plaque" development using multiple regression analysis (R2 = 0.989). Thus, FEA applied in vivo is a sensitive and highly informative diagnostic technique for detection of triggered atherosclerotic plaque disruption and related structural changes, associated with plaque transformation, in a rabbit model.     

Surface functionalization of ordered mesoporous carbons--a comparative study

Hexagonally structured mesoporous carbons C15 and CMK-5 and cubically structured carbon C48 were synthesized using ordered silica SBA-15 and MCM-48 as templates and carbon precursors of different structures. The surfaces of these ordered carbons were chemically functionalized by employing an approach, in which the selected diazonium compounds were in situ generated and reacted with the carbon frameworks of the mesoporous carbons. The aromatic organic molecules containing chlorine, ester, and alkyl groups were covalently attached to the surface of these ordered mesoporous carbons. The presence of functional groups on the modified carbons was confirmed with Fourier transform infrared spectroscopy, thermogravimetric analysis, and nitrogen adsorption. The BET-specific surface area and the pore width of ordered carbons were significantly reduced, whereas the primary structure of these ordered carbons and their unit cells were intact. Basically, the density of grafted functional groups is related to the specific surface area of the sample, particularly the surface area of mesopores. The surface functionalization reaction takes place only on the external surface of carbon C15, while it occurs on both of the internal and external surface of CMK-5 carbon with the nanopipe structure. The presence of the micropores in CMK-5 carbon should be responsible for its lower grafting density because the small micropores are inaccessible in the reaction. It was also proposed that the preferred adsorption/reaction in C48 may be related to the observed unsymmetrical degradation of the XRD patterns for the functionalized C48 samples. The chemical modification process considerably reduced the primary mesopores in these ordered carbons by approximately 1-1.5 nm, affording carbons with micropores in the cases of C15 and C48, and mixed micropores and small mesopores in the case of CMK-5. A grafting density of approximately 0.9-1.5 micromol/m(2) was achieved under current research.     

基于双波测量的催化动力学极诸法测定钒

在 ｐＨ ４．５ ＨＡｃ－ＮａＡｃ缓冲溶液中，钍试剂分别于－ ０．３６ Ｖ、－ ０．６０ Ｖ产生两个灵敏的极谱波。基于钒对溴酸钾氧化钍试剂的催化作用，建立了双极谱波测量的催化动力学极谱法。钒浓度在０．７～１５μｇ／Ｌ与△Ｉ（△Ｉ１＋ Ｉ２）呈线性关系，检测限为０．５μｇ／Ｌ。研究了极谱波性质及电极反应机理。本法简便、灵敏、准确，已用于直接测定水中痕量钒。     

硅酸及其盐的研究 ⅩⅩⅠ.三甲基硅烷化-气相色谱法测定单硅酸的离解常数

单硅酸的离解常数是表征其基本性质的重要数据,前人已有不少工作,但由于测定的方法和实验条件不同,所得数据很不一致。     

DNA-modified electrodes; part 4: optimization of covalent immobilization of DNA on self-assembled monolayers

The covalent immobilization of DNA onto self-assembled monolayer (SAM) modified gold electrodes (SAM/Au) was studied by X-ray photoelectron spectrometry and electrochemical method so as to optimize its covalent immobilization on SAMs. Three types of SAMs with hydroxyl, amino, and carboxyl terminal groups, respectively, were examined. Results obtained by both X-ray photoelectron spectrometry and cyclic voltammetry show that the largest covalent immobilization amount of dsDNA could be gained on hydroxyl-terminated SAM/Au. The ratio of amount of dsDNA immobilized on hydroxyl-terminated SAMs to that on carboxyl-terminated SAMs and to that on amino-terminated SAMs is (3-3.5): (1-1.5): 1. The dsDNA immobilized covalently on hydroxyl-terminated SAMs accounts for 82.8-87.6% of its total surface amount (including small amount of dsDNA adsorbed). So the hydroxyl-terminated SAM is a good substrate for the covalent immobilization of dsDNA on gold surfaces.     

Synthesis and Magnetism of 2-Hydroxy-1,3-propylene-bis(oxamato)-bridged Co~ⅡCu~ⅡCo~Ⅱ Complexes

ＳｙｎｔｈｅｓｉｓａｎｄＭａｇｎｅｔｉｓｍｏｆ２┐Ｈｙｄｒｏｘｙ┐１，３┐ｐｒｏｐｙｌｅｎｅ┐ｂｉｓ（ｏｘａｍａｔｏ）┐ｂｒｉｄｇｅｄＣｏⅡＣｕⅡＣｏⅡＣｏｍｐｌｅｘｅｓＭＩＡＯＭｉｎｇ－ｍｉｎｇ，ＣＨＥＮＧＰｅｎｇ，ＬＩＡＯＤａｉ－ｚｈｅｎｇＪＩＡ...     

取代基效应与乙烯-α-烯烃共聚物的序列结构——5.乙烯-乙烯醇共聚物

本文应用取代基效应(SCS)方法研究了乙烯-乙烯醇(EVA)共聚物,得到了羟基(-OH)在两种不同溶剂中的SCS参数:在苯酚+重水(80/20W/W)中参数为S_1=42.77±0.08ppm,S_2=7.155±0.06ppm,S_3(s)=-4.08±0.02ppm,S_3(t)=-3.09±0.02ppm,S_4=0.48±0.03ppm,S_5=0.26±0.05ppm,在以邻二氯苯为溶剂时参数为S_1=44.97±0.61ppm,S_2=7.40±0.00ppm,S_3(s)=-4.51±0.17ppm,S_3(t)=-3.13±0.00ppm,S_4=0.63±0.04ppm,S_5=0.36±0.00ppm,同时利用所得到的SCS参数对该共聚物的~(13)C NMR谱进行了归属。