微波消化-连续流动进样冷原子吸收法测定中成药中痕量汞

本实验室建立了用微波消化系统，消化中成药样品，用连续流动进样冷原子吸收法测定了中成药中痕量汞的方法。研究了硝酸－过氧化氢和硝酸－硫酸－高氯酸两种不同混合酸的消化体系及消化时间和压力对测定结果的影响。方法的相对标准偏差为４．９％，回收率在９１％—１１６％之间，检出限为０．１５ｎｇ／ｍＬ。     

Investigation on Interaction between Cold Plasma with Catalysts

The characteristic parameters were measured with floating double probe method when cold plasma was interacting with catalysts,such as MoO3/Al2O3,NiY,Pd/Al2O3,which were used in the conversion of natural gas to C2 hydrocabons through electrical field enhanced plasma catalysis.These parameters were compared in different input voltage,different atmosphere,before and after reaction in plasma field.The interaction between catalysts and cold plasma was also investigated.This confirm that cold plasma can enhanced catalysis effect.     

Determination of mercury in saliva with a flow-injection system

A simple, fast and reliable method, with a low detection limit, has been developed for the determination of total mercury in saliva samples. The method uses a brominating reagent, followed by on-line addition of KMnO₄ at room temperature to convert organically bound mercury to inorganic mercury ions, and determines mercury by flow-injection cold-vapour atomic absorption spectrometry. Using the method described, complete recoveries of five mercury compounds from saliva were attained. Results obtained on real samples using the new method were comparable to that obtained using the established method with batch system. The detection limit of this method, based on three standard deviations of the blank, is 0.05 μg l⁻¹ Hg in a saliva sample of 500 μl. A sample throughput of 80 measurements per hour is possible with the method. The calibration curves are linear up to 20 μg l⁻¹ and the dynamic range extends to 40 μg l⁻¹ Hg. At a concentration of 1μg l⁻¹ mercury in saliva, the relative standard deviation is about 2% for 11 replicates; a total volume of 0.5 ml saliva is required for three replicates.     

Evaluation of 3,5-stigmastadiene content of edible oils: Comparison between the traditional capillary gas chromatographic method and the on-line high performance liquid chromatography-capillary gas chromatographic analysis

Summary The quantitation of 3,5-stigmastadiene and other steroidal hydrocarbons, commonly known as steradienes, is a valid tool for the recognition of refining (in particular bleaching) of edible oils; the evidence of this process is nowadays of a great interest due to growing market for virgin, cold-pressed, natural oils. Due to the long time required (about 4 hours) and the amount of solvents employed (about 650 mL) to perform the official analysis, other methods have been recently proposed, the most important of which involves high performance liquid chromatography coupled with capillary gas chromatography (HPLC-GC). In this study the results of ten oil samples, analysed by both the official method and HPLC-GC, are reported and the two methods compared and discussed, for routine use, in terms of sample preparation, time of analysis and setting up, difficulty and reproducibility.     

Determination of amino acids in the hepatic and brain tissue of the rat by gas chromatography

A procedure is described for the quantitative determination of amino acids in hepatic and brain tissue samples from the rat. Because the presence of certain matrix components in the tissue material led to interference with chromatographic analysis they were removed by a prechromatographic “clean-up” step. Quantitative analysis of amino acids, as their N-heptafluorobutyryl iso-butyl ester derivatives, was achieved by high resolution gas chromatography on an apolar fused silica open tubular column. Reproducibility data from the complete procedure are presented; coefficients of variation for arginine and histidine in hepatic tissue varied between 7.1 and 10.1% whereas those for most other amino acids were better than 5%, with a mean recovery of 90%.     

Comparison of batchstirred and electrospray reactors for biodesulfurization of dibenzothiophene in crude oil and hydrocarbon feedstocks

Biological removal of organic sulfur from petroleum feedstocks offers an attractive alternative to conventional thermochemical treatment, because of the mild operating conditions afforded by the biocatalyst. In order for biodesulfurization to realize commercial success, reactors must be designed that allow for sufficient liquid-liquid and gas-liquid mass transfer, while simultaneously reducing operating costs. Electro-spray bioreactors were investigated for use as desulfurization reactors because of their reported operational cost savings relative to mechanically agitated reactors. Unlike batch-stirred reactors, which mix the biocatalystcontaining aqueous phase with the organic feedstock by imparting momentum to the entire bulk solution, electro-spray reactors have the potential for tremendous cost savings, creating an emulsion <5 (μm in diameter, at a cost of only 3 W/L. Power law relationships indicate that mechanically stirred reactors would require 100-1000-fold more energy to create such a fine emulsion, but these relationships generally do not account for the effect of endogenously produced surfactant in the system. Here, the rates dibenzothiophene (DBT) oxidation to 2-hydroxybiphenyl (2-HBP) in hexadecane, byRhodococcus sp IGTS8 are compared in the two reactor systems. Desulfurization rates ranged from 1.0 to 5.0 mg 2-HBP/(dry g cells · h), independent of the reactor employed. The batch-stirred reactor was capable of forming a very fine emulsion in the presence of the biocatalyst IGTS8, similar to that formed in the emulsion phase contactor (EP^TM), presumably because the biocatalyst produces its own surfactant. Although EPC did not prove to be advantageous for the IGTS8 desulfurization system, it may prove advantageous for systems that do not produce surface-active bioagents, in addition to being mass-transport limited.     

Spectroscopic study of the reaction of tetramethyldisiloxane with a cold remote nitrogen plasma. Effect of dioxygen addition in the reactive mixture

The interaction of 1,1,3,3-tetramethyldisiloxane with a cold remote nitrogen plasma is studied by visible ultraviolet emission spectroscopy. Evolutions of emissions when dioxygen is added in the remote plasma region are correlated with the previously studied main characteristics of the polymeric deposition. The role of the energy vectors is discussed. New emissions are attributed to the triatomic Si O Si molecule.     

Melting and glass transitions in paraffinic and naphthenic oils

Naphthenic and paraffinic oils were analyzed by modulated differential scanning calorimetry (MDSC). The results showed several improvements in the analysis of thermal properties when compared with standard DSC. The glass transition temperature (T_g), the enthalpy relaxation at T_g, and the melting endotherms could be deconvoluted, and reversible melting could be identified. This allowed for an easier interpretation of the thermal properties of the oils. With MDSC, the T_gs in mineral oils were found to coincide with endothermic enthalpy relaxation, which is generally regarded as a melting endotherm with standard DSC. A decrease in heat capacity after T_g was attributed to the existence of rigid amorphous material. From Δc_p at T_g and the oil molecular weight, the number of repeat units in the oil chains was estimated at less than 20. The T_g of a hypothetical pure aromatic oil was found to be similar to that for petroleum asphaltenes, and that for a naphthenic oil of infinite molecular weight to be similar to that of petroleum resins.     

Determination of mercury in biological samples by cold vapor atomic absorption spectrometry following cloud point extraction with salt-induced phase separation

Method development for the pre-concentration of mercury in human hair, dogfish liver and dogfish muscle samples using cloud-point extraction and cold vapor atomic absorption spectrometry is demonstrated. Before the extraction, the samples were submitted to microwave-assisted digestion in a mixture of H₂O₂ and HNO₃. Cloud point extraction was carried out using 0.5% (m/v) ammonium O,O-diethyldithiophosphate (DDTP) as the chelating agent and 0.3% (m/v) Triton X-114 as the non-ionic surfactant. Phase separation was induced after the addition of Na₂SO₄ to a final concentration of 0.2 mol L⁻¹. Aliquots of the final extract were transferred to PTFE tubes and NaBH₄ and HCl were added. The mercury vapor was driven to a non-heated quartz tube for measuring the absorbance. The results obtained with salt-induced phase separation were in good agreement with the certified values at a 95% confidence level. An enrichment factor of 10 allowed a detection limit of 0.4 ng g⁻¹ to be obtained, which demonstrates the high sensitivity of the proposed procedure for the determination of mercury at trace levels.     

冷原子荧光法间接测定水中氰化物

本文详细研究了氰化物蒸馏条件及其稳定性问题，建立了一个冷原子荧光法间接测定水中氰化物的方法，并用于海水及氰化液中痕量ＣＮ－的测定，结果令人满意。ＣＮ－检出限为０．０２μｇ／ｍＬ，回收率９５％～９８％，变异系数７．３％～８．９％。