高速非达西流动时元素硫沉积模型研究

元素硫沉积是含硫气藏开发过程中广泛存在而又必须解决的难题之一。高含硫气藏一旦投入开发，地层压力会逐步下降，使得元素硫溶解度下降而沉积下来，沉积的元素硫会堵塞地层孔隙，降低渗流通道，影响气井产能。考虑了高含硫气体在近井地带作高速非达西流动，建立了硫的沉积模型，并利用该模型对实际气藏进行预测和对比研究，再通过实例计算发现，硫非瞬时平衡沉积比瞬时平衡沉积对地层的伤害更严重，高速非达西流动沉积比达西流动时对地层伤害更严重，认为在开发高含硫气藏时，必须合理选择开发速度，有效防止元素硫沉积。     

超低硫燃料柴油的润滑性研究与性能研究

研究提出了超低硫燃料暂定战术技术指标，并规定了其润滑性要求。通过对基础油生产工艺研究、柴油润滑性添加剂研究及配方性能评定，成功研制了一种环保型超低硫燃料，满足外燃发动机（燃烧室高温高压）的使用要求。研制产品具有馏分窄、闪点高、氧化安定性好、低温性能优异、硫含量超低、润滑性能好等特点。燃料的低硫化是燃料发展的必然趋势。在我国开展低硫或超低硫环保型燃料研制，同时开展燃料润滑性添加剂的研制，具有重要意义。     

Interfacial activity and rate of palladium(II) extraction with decyl pyridine monocarboxylates

Decyl isonicotiniate and decyl nicotiniate permit a rapid extraction of palladium(II) from its hydrochloride solutions. Decyl picoliniate is not a suitable extractant. 4-Octylphenylamine can act as a phase transfer catalyst when its concentration in the organic phase is at least 2·5 × 10^?4 M . It seems that the interfacial adsorption of pyridine carboxylates and of 4-octylphenylamine is not the decisive phenomenon in palladium(II) extraction. The negligible protonation of the pyridine-type extractants and the phase transfer catalysis explains well the quick extraction of palladium(II) with the commercial and highly hydrophobic extractant ACORGA CLX-50.     

我国车用无铅汽油的质量状况及分析

对1998－2001年间生产领域和流通领域的近500批次汽油产品检验数据进行了总结和分析，表明我国汽油的实物质量正在不断提高，但从环保要求出发还需不断向国际水平靠扰，尤其应进一步降低烯烃含量，硫含量。     

制备低硫可膨胀石墨的研究

研究了以过二硫酸铵作氧化剂低硫可膨胀石墨的制备，找到了在较低温度下，制备低硫可膨胀石墨的最佳条件。即过二硫酸铵和石墨的重量比为１５％；反应温度为５５℃；反应时间为４０ｍｉｎ；硫酸浓度为９８％；硫酸与石墨的重量比为４∶１，草酸和硝酸（浓度为６５％）的重量比为７．５％时，所制得的可膨胀石墨含硫量为０．６５％，膨胀容积为２００ｍＬ／ｇ可膨胀石墨。并且，其终端产品柔性石墨具有优良的力学性能和抗氧化性能。     

A ctivation measurement of neutron distribution in intermediate energy heavy ion target area

The distribution of neutrons produced by the reaction of 50MeV/u ^12C-ion on a thick Cu target are studied.The neutrons are measured with threshold activation detectors.Al.F,C,Al and In activation samples were used to measure neutrons with energy greater than 7,11,20,50MeV and thermal neutrons,respectively,The fluence rate,energy and angular distributions of neutrons,total neutron yield of 12C-ion and the emission rate in the forward direction of neutrons over 11 and 20MeV were obtained.     

有机磷灭蚊剂投放浓度和时间对水体总磷的影响

为分析新型低毒有机磷杀虫剂“1%双硫磷颗粒”投放对河道水质的影响,设置不同药剂投放浓度和不同反应时间的室内试验,以TP、NH₃-N及S^2-为目标因子,分析该药剂投放后水体污染物浓度。结果表明:不同试验组水样中S^2-质量浓度均小于0.02 mg/L,NH₃-N质量浓度处于0.029~0.036 mg/L之间,均达到地表水Ⅰ类标准;不同浓度药剂投放1 h后,水体TP质量浓度已达到稳定状态,且在60 h内均保持稳定,药剂投加量与水体TP质量浓度呈显著正相关(R²=0.85);不同处理组的药剂在水体中的TP释放量无明显差异,均在1.06~1.30 mg/g之间。“1%双硫磷颗粒”推荐适宜投放量不会使河道水质恶化到劣Ⅴ类,但增加药剂投放量会增加水体TP污染及富营养化风险。     

Thermal diffusivity of fluids in a broad region around the critical point

Dynamic light scattering is a suitable method for the investigation of transport properties such as the thermal diffusivity of optically transparent fluids. The main advantages of the method are its quickness, the fact of the thermodynamic state of equilibrium of the sample (gradients are not required), and the relatively simple evaluation of data without the necessity of calibration. However, an insufficient production of intensity of scattered light may be a limiting effect. For that reason the vicinity of the gas-liquid critical point represents the classical range of application. In this paper, it is shown that by means of an appropriate choice of experimental apparatus, measurements are also feasible in an extended range of states. Broad regions around critical points of three pure fluids (sulfur hexafluoride, SF₆; ethane, C₂H₆; nitrous oxide, N₂O) over temperature ranges ¦T-T _c¦ of 0.02 to 50 K and density ranges (/_c) of 0.2 to 2 were investigated. In this region the thermal diffusivity shows great variations with temperature and density and cannot be described by means of ideal-gas behavior or relations for liquids. The measurements were carried out along the coexistence curve for both phases, along the critical isochore and along some isotherms with TT _c. The measured or calculated density, pressure, and thermal diffusivity data as well as some correlations are presented.     

硫掺杂ZnFe2O4/蒙脱石复合材料的铀酰吸附研究

为获得铀酰(UO2²⁺)吸附性能高的吸附剂,以蒙脱石(Montmorillonite,MMT)和铁酸盐(ZnFe₂O₄)为原材料与L-半胱氨酸通过水热反应制备了硫掺杂ZnFe₂O₄(S-ZnFe₂O₄)和ZnFe₂O₄/MMT(S-ZnFe₂O₄/MMT),采用XRD、FTIR和SEM对S-ZnFe₂O₄和S-ZnFe₂O₄/MMT进行了结构表征,研究了pH、接触时间和UO2²⁺初始质量浓度对UO2²⁺吸附效果的影响,结果表明:S-ZnFe₂O₄呈高分散的纳米颗粒状,并且均匀分布于蒙脱石片层结构表面;S-ZnFe₂O₄与蒙脱石复合后能明显提高其UO2²⁺吸附性能,最佳吸附pH为6.0;S-ZnFe₂O₄和S-ZnFe₂O₄/MMT复合材料对UO2²⁺的最大吸附量分别为51.44 mg/g和68.45 mg/g;吸附符合Langmuir等温吸附模型和伪二阶动力学模型,说明吸附过程属于表面单分子层化学吸附。     

Oxidation of Hydrogen Sulfide by Quinones: How Polyphenols Initiate Their Cytoprotective Effects

We have shown that autoxidized polyphenolic nutraceuticals oxidize H₂S to polysulfides and thiosulfate and this may convey their cytoprotective effects. Polyphenol reactivity is largely attributed to the B ring, which is usually a form of hydroxyquinone (HQ). Here, we examine the effects of HQs on sulfur metabolism using H₂S- and polysulfide-specific fluorophores (AzMC and SSP4, respectively) and thiosulfate sensitive silver nanoparticles (AgNP). In buffer, 1,4-dihydroxybenzene (1,4-DB), 1,4-benzoquinone (1,4-BQ), pyrogallol (PG) and gallic acid (GA) oxidized H₂S to polysulfides and thiosulfate, whereas 1,2-DB, 1,3-DB, 1,2-dihydroxy,3,4-benzoquinone and shikimic acid did not. In addition, 1,4-DB, 1,4-BQ, PG and GA also increased polysulfide production in HEK293 cells. In buffer, H₂S oxidation by 1,4-DB was oxygen-dependent, partially inhibited by tempol and trolox, and absorbance spectra were consistent with redox cycling between HQ autoxidation and H₂S-mediated reduction. Neither 1,2-DB, 1,3-DB, 1,4-DB nor 1,4-BQ reduced polysulfides to H₂S in either 21% or 0% oxygen. Epinephrine and norepinephrine also oxidized H₂S to polysulfides and thiosulfate; dopamine and tyrosine were ineffective. Polyphenones were also examined, but only 2,5-dihydroxy- and 2,3,4-trihydroxybenzophenones oxidized H₂S. These results show that H₂S is readily oxidized by specific hydroxyquinones and quinones, most likely through the formation of a semiquinone radical intermediate derived from either reaction of oxygen with the reduced quinones, or from direct reaction between H₂S and quinones. We propose that polysulfide production by these reactions contributes to the health-promoting benefits of polyphenolic nutraceuticals.