气相色谱-三重四级杆质谱测定环境样品中17种二 英

研究了基于Agilent气相色谱-三重四级杆质谱测定环境样品中17种二 英的分析方法.结果表明,在浓度范围0.5~2000ng/mL之间具有良好的线性,17种二 英的相对响应因子在0.96~1.21之间,相对标准偏差< 14%,定量限范围在0.080~2.83pg/μL之间,适合环境样品中超痕量二 英的分析.利用该方法对第15轮二 英国际实验室比对的沉积物样品进行了测试,总I-TEQ值落在Intercal给定的中位值±标准偏差范围内.研究选取污染源烟道气、飞灰、土壤和沉积物等40多个环境样品进行测试,并与高分辨质谱测定结果比较表明,当环境样品中二 英浓度在0~60ng I-TEQ范围,两者数据具有较好的线性相关性,R2=0.997.就17种单体而言,利用三重四级杆质谱测定的2,3,7,8-TCDF和1,2,3,7,8,9-HxCDF结果会高于高分辨质谱,而1,2,3,7,8,9-HxCDD的结果低于高分辨质谱的测定值.鉴于三重四级杆质谱在购置、维护和能耗等方面的低成本优势,本方法可作为简易经济的环境中超痕量二 英的分析方法.     

Limiting explosible concentration of hydrogen–oxygen–helium mixtures related to the practical operational case

This paper presents data on the limiting (minimum) concentrations of hydrogen in oxygen, in the presence of added helium, at elevated temperature and pressure related to the practical operational case. A 5 L explosion vessel, an ignition sub-system and a transient pressure measurement sub-system were used. Through a series of experiments carried out using this system, the limiting concentrations of hydrogen in oxygen and helium at different initial pressures and temperatures for the practical operational case were studied, and the influence of ignition energy and initial temperature on the limiting concentration of hydrogen in oxygen and helium was analyzed and discussed. The variation of ignition energy within the studied range is found to have a significant effect on the limiting concentration of hydrogen in oxygen and helium at lower initial temperature. However, when the ignition energy is higher than 32 mJ, the limiting hydrogen concentration remains almost changeless as the initial temperature increases from 21 °C to 90 °C. The limiting explosible concentration of hydrogen–oxygen–helium mixture decreases as the ignition energy increases when the initial temperature is lower. When the initial temperature is higher, the ignition energy has little effect on the limiting hydrogen concentration of hydrogen–oxygen–helium mixtures. When the initial temperature reaches 90 °C, the limiting hydrogen concentration remains almost changeless with an increase in ignition energy. The limiting explosible concentration of hydrogen in the mixtures, at the initial temperature of 21 °C and the ignition energy of 0.5 mJ, is 8.5% and that of oxygen is 11.25%.     

Dynamic behavior of direct spring loaded pressure relief valves in gas service: Model development,measurements and instability mechanisms

A synthesis of previous literature is used to derive a model of an in-service direct-spring pressure relief valve. The model couples low-order rigid body mechanics for the valve to one-dimensional gas dynamics within the pipe. Detailed laboratory experiments are also presented for three different commercially available values, for varying mass flow rates and length of inlet pipe. In each case, violent oscillation is found to occur beyond a critical pipe length, which may be triggered either on valve opening or closing. The test results compare favorably to the simulations using the model. In particular, the model reveals that the mechanism of instability is a Hopf bifurcation (flutter instability) involving the fundamental, quarter-wave pipe mode. Furthermore, the concept of the effective area of the valve as a function of valve lift is shown to be useful in explaining sudden jumps observed in the test data. It is argued that these instabilities are not alleviated by the 3% inlet line loss criterion that has recently been proposed as an industry standard.     

Optimization of HSE in maintenance activities by integration of continuous improvement cycle and fuzzy multivariate approach: A gas refinery

Gas refineries have been continuously focusing on Health, Safety and Environment programs to improve maintenance activities. Several researches have studied on this area with different analysis methods. This study presents an integrated approach for optimization of factors contributing to the implementation of Health, Safety and Environment (HSE) in maintenance activities. HSE managers in each sector answered standard questionnaire whit respect to HES. The methodology is based on fuzzy data envelopment analysis (FDEA) and Deming's continuous improvement cycle. Also, this method is used to rank the relevant performance efficiencies in certain and uncertain conditions of each HSE sectors whit considering HSE in maintenance activities. It corresponds and integrates its registered HSE-MS with OHSAS 18001:2007 and ISO 14001:2004 to evaluate multiple inputs and outputs of over 36 subsidiary HSE divisions with parallel mission and objectives simultaneously. Also, it determines efficient target indices and could assure continuous improvement in the organization. This is the first study that introduces an integrated approach to improve HSE management programs in a gas refinery by a robust and continuous improvement approach.     

Thermodynamic investigation and hydrate inhibition of real gas flow through orifice during depressurization

A thermodynamic procedure has been proposed which can be used to predict the gas pressure, temperature and flow rate through orifice upon chock flow condition, using equation of state (EOS). The procedure applied for emergency depressurization operation incorporating the Peng-Robinson EOS and validated by comparing flow rates of a multi-component hydrocarbon gas mixture for thirteen experimental cases. The average absolute deviations of the predicted flow rates for orifice discharge coefficients of 0.85 and 0.9, are 7.36% and 2.03%, respectively. The corresponding error for API 520 (American Petroleum Institute Recommendation Practice 520) method is 6.91%. In this work, the hydrate formation temperature and hydrate inhibitor type and its required weight fraction for preventing the hydrate formation upon orifice and its upstream conditions are evaluated by the EZ-Thermo software using the Moshfeghian–Maddox method. The results qualitatively show that the hydrate prevention is essential for the safety of the operation due to low temperature condition.     

加强发证检验工作确保海上石油生产安全

针对国家关于海上石油天然气生产设施检验和石油作业安全管理的相关规定,结合胜利油田开展发证检验工作的实际情况。对当前海上石油生产设施发证检验过程中存在的问题进行了探究,并提出了相应的对策建议。     

Automated indirect fluoride determination by ICP-OES using discontinuous-flow analysis

An automated method for the indirect determination of fluoride by inductively coupled plasma atomic emission spectrometry using discontinuous-flow analysis has been developed. A modified flow injection analysis system was used for sample preparation. The method is based on the determination of excess cerium(III) ion after precipitation of CeF₃. Separation of the precipitate is performed online on a syringe membrane filter that is cleaned each analysis cycle by 1 M nitric acid, ensuring a long life-time for the filter. As a result of the short reaction time, a detection limit of 9.5 mg L^?1 was obtained. The precision (RSD) of the proposed method is 1.02% at fluoride concentration of 28 mg L^?1. The applicability of the technique for groundwater monitoring of fluoride-contaminated area is demonstrated.     

Determination of mercury and arsenic levels in fish caught in the Beheshtabad River,Chaharmahal and Bakhtiari Province,Iran

Mercury and arsenic pollution has been recognized as a potential environmental and public health problem for over 40 years. The major source of exposure to mercury for humans is the ingestion of fish. This study was conducted with the aim of determining the levels of mercury and arsenic in the muscles of four fish species caught in the Beheshtabad River and comparing the results with the maximum tolerance levels for mercury and arsenic. The samples of 90 fish were used for the determination of both the metals by graphite furnace atomic absorption spectrometry. The results showed that the concentrations ranged from 1.5 to 3.8 µg kg^?1 for mercury and from 35 to 70 µg kg^?1 for arsenic, with means of 2.7 ± 0.5 and 57 ± 12 µg kg^?1, respectively. Both mean levels were lower than the threshold limits acceptable by WHO standards.     

Oxidized multiwalled carbon nanotubes modified with 2-(2-hydroxy-5-nitrophenyl)-4,5-diphenyl imidazole for solid phase extraction and preconcentration of some metal ions

In this work, a new procedure for the enrichment of the trace amount of Cu²⁺, Ni²⁺, Co²⁺, Pb²⁺, Fe²⁺, and Zn²⁺ ions based on the utilization of multiwalled carbon nanotubes (MWCNT) modified with 2-(2-hydroxy-5-nitrophenyl)-4,5-diphenyl imidazole as chelating agent prior to their determination by flame atomic absorption spectrometry has been described. The influence of effective parameters including pH, amount of ligand and MWCNT, composition of eluent, and coexisting ions on recoveries of understudy metal ions was examined. At the optimum pH of 5.0, all metal ions were quantitatively sorbed onto the proposed solid phase and completely desorbed with 8?mL of 5.0?mol?L^?1 HNO₃. The detection limit of Cu²⁺, Co²⁺, Ni²⁺, Pb²⁺, Fe²⁺, and Zn²⁺ ions was 1.7, 2.4, 2.3, 2.9, 2.8, and 1.4?µg?L^?1, while the preconcentration factor was 63 for Cu²⁺ and 94 for the other metal ions and relative standard deviations between 1.8 less than 3.0%. The proposed procedure was applied for the analysis of various samples.     

Assessment of potentially toxic elements in Swiss chard and sediments of Akaki River,Ethiopia

For the determination of 15 potentially toxic elements (V, Cr, Fe, Mn, Co, Ni, Cu, Zn, As, Se, Ag, Cd, Sn, Hg, and Pb) in plant and sediment samples of the Akaki River, Ethiopia, inductively coupled plasma–mass spectrometry, inductively coupled plasma–optical emission spectrometry, and a RA-915+ mercury analyzer were applied. Sediment and plant samples were mineralized using a closed-vessel microwave-assisted digestion system. The elemental concentrations varied considerably in plant and sediment samples. The minimum concentration was observed for known toxic elements (As, Hg, and Cd) while the highest concentration was observed for the elements of relatively low toxicity Zn, Mn, and Fe. The concentration of Cr, Fe, Pb, Zn, and As in Swiss chard surpassed the maximum permissible levels at specific sites. At some of the sites, the sediment quality guidelines are surpassed for Cu, Zn, and Pb.