Anti-ulcer activity of Smithia conferta in various animal

Smithia conferta Sm. (Leguminasae), is a commonly used plant in Indian traditional medicine. In the current study anti-ulcer activity of its petroleum ether, alcohol and aqueous extracts of leaves were investigated using different animal models. All extracts were also subjected to phytochemical analysis and their toxic potential. Petroleum ether extract was found to contain steroids; alcohol extract revealed the presence of isoflavonoids, alkaloids and carbohydrates; while aqueous extract was found to contain amino acids, carbohydrates and flavonoids. S. conferta aqueous and alcoholic extracts were found to be non-toxic up to 5000 mg/kg dose level while petroleum ether extract was safe only up to a dose of 2000 mg/kg after single dose administration of the extracts.During confirmation of the claimed anti-ulcer activity, treatment with aqueous and alcoholic extracts showed significant reduction in ulcer index, free acidity as well as total acidity in pylorus ligated rats. However, petroleum ether extract showed relatively less profound reduction in all these indices. The anti-ulcer activity observed in aqueous extract treatment group was nearly equivalent to the standard group.     

基于云理论的我国光伏产业产能过剩评估研究

基于云理论的评价方法,构建指标体系,利用云重心理论求出各指标的云模型,计算与理想状态向量的加权偏离度,以此衡量我国光伏产业产能过剩程度.该评价理论提高了评价结果的准确性,评价结果与实际情况吻合,表明该评价指标与评价方法具有较强的可操作性和科学性,并就此对光伏产业产能过剩的治理,提出了政策建议.     

基于信息显著性差异的绿色产业评价指标筛选模型及实证

依据广义的绿色产业内涵,通过信息显著性差异与信息冗余分析定量筛选指标,建立了包括绿色生产指标层、绿色生态环境指标层、绿色消费方式指标层的大连市绿色产业评价指标体系。本文的创新与特色一是通过负载系数大小差异进行信息显著性分析,删除负载系数小、对综合评价结果影响弱的指标。克服了现有研究先进行相关分析剔除冗余指标,再利用负载系数大小差异筛选出反映信息显著性大的指标的弊端。事实上,指标间较高的相关性是计算负载系数的必要前提。因此,利用负载系数筛选指标前是不可进行指标的相关分析降低指标间的相关性的。二是通过结合专家知识经验辨析指标的实际含义,仅对反映信息可能重复的指标使用相关分析,剔除同指标层内相关系数较大的两个指标中反映指标层信息能力相对较弱的指标。克服了仅仅通过相关系数不能准确衡量指标间信息重复程度的弊端。研究结果表明,最终建立的指标体系通过25．68％的指标反映了97．09％的原始信息。通过与同类的指标体系进行对比,对大连市绿色产业评价指标体系的合理性做了进一步的分析。     

Aggregate production planning for process industries under oligopolistic competition

We consider a competitive version of the traditional aggregate production planning model with capacity constraints. In the general case, multiple products are produced by a few competing producers (oligopoly) with limited capacities. Production quantities, prices and consequently profits depend on production and allocation decisions of each producer. In addition, there is competition for the raw material whose supplies are limited, and where prices reflect these limitations. Such situations have recently occurred in several process industry settings including petro-refining, petrochemicals, basic chemicals, cement, fertilizers, pharmaceuticals, rubber, paper, food processing and metals. We use a successive “Bertrand–Cournot” framework to address this problem and to determine optimal production quantities, prices and profits at the producers and at the raw material supplier. Our analysis allows a new way to understand and evaluate the marginal value of additional capacity when there is competition for the market and raw materials.     

Preparation of mesophase pitch doped with TiO2 or TiC particles

The co-pyrolysis of a petroleum residue with two different sources of titanium (tetrabutyl-ortotitanate (TBO) or titanium carbide nano-powder) was carried out to obtain mesophase pitches containing TiO₂ or TiC nanoparticles. Co-pyrolysis is an appropriate technique to achieve a good dispersion and low particle size. In the case of TBO, TiO₂ nanoparticles (5–20 nm) are observed, which are forming aggregates, the largest of them being 1–2 μm. In the case of TiC nano-particles, they are more difficult to disperse and larger aggregates are formed, although the final material is rather homogenous. The chemistry of pyrolysis for the production of doped and undoped mesophase pitches has been followed by means of solvent insolubility, XRD, XPS, FTIR and elemental analysis. They show evidences of promotion of the formation of mesophase in the presence of the titanium-containing particles, especially in the presence of TiO₂. The final materials can be of great value as precursors to produce high density titanium doped graphites for nuclear and space applications.     

Industrial Applications of Mössbauer Spectroscopy

Hyperfine Interactions - The historical development of the use of Mössbauer spectroscopy in industrial applications is briefly outlined. The power of the technique for the study of...     

Feasibility of high-resolution continuum source molecular absorption spectrometry in flame and furnace for sulphur determination in petroleum products

For the first time, high-resolution molecular absorption spectrometry with a high-intensity xenon lamp as radiation source has been applied for the determination of sulphur in crude oil and petroleum products. The samples were analysed as xylene solutions using vaporisation in acetylene-air flame or in an electrothermally heated graphite furnace. The sensitive rotational lines of the CS molecule, belonging to the ?ν = 0 vibrational sequence within the electronic transition X¹∑⁺ → A¹П, were applied. For graphite furnace molecular absorption spectrometry, the Pd + Mg organic modifier was selected. Strong interactions with Pd atoms enable easier decomposition of sulphur-containing compounds, likely through the temporal formation of Pd_xS_y molecules. At the 258.056 nm line, with the wavelength range covering central pixel ± 5 pixels and with application of interactive background correction, the detection limit was 14 ng in graphite furnace molecular absorption spectrometry and 18 mg kg⁻¹ in flame molecular absorption spectrometry. Meanwhile, application of 2-points background correction found a characteristic mass of 12 ng in graphite furnace molecular absorption spectrometry and a characteristic concentration of 104 mg kg⁻¹ in flame molecular absorption spectrometry.The range of application of the proposed methods turned out to be significantly limited by the properties of the sulphur compounds of interest. In the case of volatile sulphur compounds, which can be present in light petroleum products, severe difficulties were encountered. On the contrary, heavy oils and residues from distillation as well as crude oil could be analysed using both flame and graphite furnace vaporisation. The good accuracy of the proposed methods for these samples was confirmed by their mutual consistency and the results from analysis of reference samples (certified reference materials and home reference materials with sulphur content determined by X-ray fluorescence spectrometry).     

Direct determination of arsenic in petroleum derivatives by graphite furnace atomic absorption spectrometry: A comparison between filter and platform atomizers

In the present work a direct method for the determination of arsenic in petroleum derivatives has been developed, comparing the performance of a commercial transversely heated platform atomizer (THPA) with that of a transversely heated filter atomizer (THFA). The THFA results in a reduction of background absorption and an improved sensitivity as has been reported earlier for this atomizer. The mixture of 0.1% (m/v) Pd + 0.03% (m/v) Mg + 0.05% (v/v) Triton X-100 was used as the chemical modifier for both atomizers. The samples (naphtha, gasoline and petroleum condensate) were stabilized in the form of a three-component solution (detergentless microemulsion) with the sample, propan-1-ol and 0.1% (v/v) HNO₃ in a ratio of 3.0:6.4:0.6. The characteristic mass of 13 pg found in the THFA was about a factor of two better than that of 28 pg obtained with the THPA; however, the limits of detection (LOD) and quantification (LOQ) were essentially the same for both atomizers (1.9 and 6.2 μg L⁻¹, respectively, for THPA, and 1.8 and 5.9 μg L⁻¹, respectively, for THFA) due to the increased noise observed with the THFA. A possible explanation for that is a partial blockage of the radiation from the hollow cathode lamp by the narrow inner diameter of this tube and the associated loss of radiation energy. Due to the lack of an appropriate certified reference material, recovery tests were carried out with inorganic and organic arsenic standards and the results were between 89% and 111%. The only advantage of the THFA found in this work was a reduction of the total analysis time by about 20% due to the ‘hot injection’ that could be realized with this furnace. The arsenic concentrations varied from < LOQ to 43.3 μg L⁻¹ in the samples analyzed in this work.     

A near-infrared spectroscopy method to determine aminoglycosides in pharmaceutical formulations

The analytical determination of aminoglycosides in pharmaceutical formulations is very difficult due to the lack of chromophores or fluorophores. Several analytical methods have been developed along the years mainly based on derivatization reactions. The European Pharmacopeia (EP) and the United States Pharmacopeia (USP) describe a microbiological assay to the quantification of aminoglycosides. Near infrared spectroscopy (NIRS) can be used alternatively to analyse aminoglycosides without the need of derivatization reactions or other type of sample processing. A new NIRS based method was developed for the analysis of the aminoglycoside antibiotic neomycin. The method was developed with samples based on a commercial formulation containing neomycin sulphate and three excipients: lactose, talc and magnesium stearate. Synthetic and doped samples were manufactured for this purpose. Three lots of a commercial solid formulation were also used to assess the validity of the method to quantify neomycin sulphate in the industrial pharmaceutical product. The method proposes measurements in reflectance mode using a Fourier-transform near infrared (FT-NIR) spectrometer. Partial least squares regression was the multivariate method adopted to calibrate the NIR spectra with the neomycin sulphate mass fraction. The concentration of neomycin sulphate present in the commercial samples was confirmed by HPLC with pre-column derivatization with phenylisocyanate. Results show that neomycin sulphate was determined successfully in the commercial samples using the method calibrated with the doped samples (mass fraction error of 6.6%). Moreover, the synthetic samples were found to be unqualified to develop the method, producing a biased calibration.