银-二乙基二硫代氨基甲酸钠法测定铁矿石中砷溶样方式的改进

改进了铁矿石样品溶解方法，尝试用硫-磷混酸溶解铁矿石样品，缩短了分析时间，提高了分析精度。溶解后的样品以银-二乙基二硫代氨基甲酸钠法（Ag—DDTC）用于部级标准物质测定，砷的测定结果与标准值相符；用于碱性矿石如球团样品中砷的分析，多名操作者的测定结果吻合。     

高效液相色谱-紫外光谱法建立3,5-二硝基苯甲酸工业品的色谱指纹图谱

建立了3，5-二硝基苯甲酸工业品的高效液相色谱-紫外光谱的指纹图谱。首先，在Kromasil C18色谱柱上，以水-甲醇-0．10％高氯酸水溶液（体积比为25：45：30）为流动相，流动相流速1．0mL／min，检测波长254nm，对3，5-二硝基苯甲酸及其相关杂质进行了分离分析。在此基础上，通过运行大量样品，筛选共有组分，绘制具有共同特性的指纹图谱。根据待测样品色谱峰的保留时间、紫外光谱及其色谱峰面积，与色谱指纹图谱进行分析对比，建立了控制3，5-二硝基苯甲酸产品质量的新方法。该方法在产品含量测定方面结果准确、可靠，在产品质量控制方面直观、方便。阐述了“整体性”和“明确性”是精细化工中间体指纹图谱的基本属性和发展方向。     

火焰原子发射光谱法测定碳化钛中微量钠

对火焰原子发射光谱法测定碳化钛中微量钠的条件进行了试验。样品用硝酸-氢氟酸溶解，在0．30mol／L硝酸介质中，以硝酸钾作消电离剂消除钠的电离干扰，饱和硼酸溶液络合试液中过量的氟离子。方法检出限为0．015μg／mL，样品加标回收率为97．6％-105．6％，方法的精密度（RSD，n=6）小于2．5％。     

Spreading of a NAPL lens in a double-porosity medium

Spreading of a non-aqueous phase liquid (NAPL) denser than water (DNAPL) lens (mound) in the unsaturated zone of double-porosity aquifer above an impervious plane boundary is investigated. The double-porosity aquifer is conceptualized as a fracture network surrounding pervious blocks. Vertical gravity equilibrium is assumed to prevail in each one of the two media, fractures and blocks. Through vertical integration, two coupled partial differential equations for the DNAPL content in each medium are obtained. The mass exchange rate between high- and low-permeability media is considered as a function of NAPL content. The dominant effect is gravity, whereas capillary forces are negligible. Analytical solutions for one-dimensional and axisymmetric problems of mound spreading are obtained.     

Stratigraphy and geochemistry of a sequence of Quaternary palaeosols in the Lower Teleki Valley,Mount Kenya,East Africa — Implications for interregional correlations

The relative weathering of a sequence of five palaesols formed in different parent materials, including bedrock of phonolitic composition, is described and assessed. The three lower palaeosols (units 3–5) are considered to be of interglacial origin. The saprolite (unit 5), in phonolite, formed prior to deposition of the lower Brunhes-age till, is considered to be as old as the Brunhes Matuyama boundary (0.73 myr). The other two palaeosols in this group (units 3 and 4), derived from loess and till, respectively, formed over middle to late Brunhes time under palaeoclimates that were wetter (and presumably warmer), and of sufficient leaching power to move clay, as well as organically complexed extractable Fe and Al. The palaeosols in unit 3 are more complex than the lower ones. Their upper and lower horizons have about the same chemical composition as the lowest two palaeosols, while the middle horizons are similar to the upper two palaeosols (units 1 and 2). Radiocarbon dates for unit 3 are considered to be too young to account for the strong weathering in the upper and lower horizons. This interpretation is supported by high D/L ratios of aspartic acid. Overlying sediments, emplaced by episodic colluvial (unit 2) and slope wash (unit 1) processes, are less weathered; the lower colluvial unit in this group was emplaced during the late stade of the last glaciation. The surface sediments were emplaced more recently during the same interval and weathered mainly during the post-glacial period. Tentative correlations with core 82PCS18 from the Canary Basin show that upper unit 3 is probably equivalent to Isotope Stage 5e, lower unit 3 to Isotope Stage 7, unit 4 to Isotope Stage 8, and unit 5 to Isotope Stage 9. Units 1 and 2 are firmly correlated with Isotope Stage 2.     

SnCl2还原冷原子吸收测定化探样品中的汞

样品经低温稀王水溶解 ,在选定的仪器条件下 ,用氯化亚锡还原 ,测定汞的吸收峰值。方法简便、快速、价廉 ,适用于大批化探样品的测定。     

Rainwater Chemistry and Wet Deposition over the Wet Savanna Ecosystem of Lamto (Côte d'Ivoire)

From the IGAC-DEBITS Africa network (IDAF), data sets on precipitation chemistry collected from the ‘wet savanna ecosystem’ site of Lamto (Côte d'Ivoire), are analyzed (1995–2002). Inorganic (Ca^{2 +}, Mg^{2 +}, Na⁺, K⁺, NH₄ ⁺, Cl^?, SO₄ ^{2 ?}, NO₃ ^?) and organic (HCOO^?, CH₃COO^?) ions content were determined using Ion Chromatography. The analyzed 631 rainfall events represent 8420.9 mm of rainfall from a 9631.1 mm total. The precipitation chemistry at Lamto is influenced by four main sources: natural biogenic emissions from savanna soils (NO _x and NH₃), biomass burning (savanna and domestic fires), terrigeneous particles emissions from dry savanna soils, and marine compounds embedded in the summer monsoon. The inter-annual variability of the weighted volume mean concentration of chemical species linked with wet deposition fluctuates by ～ 20% over the period. Ammonium concentration is found to be the highest (17.6 μ eq.l^{? 1}) from all IDAF sites belonging to the West Africa ecosystems. Ammonia sources are from domestic animals, fertilizers and biomass burning. In spite of the high potential acidity of 30.5 μ eq.l^{? 1} from NO₃ ^?, SO₄ ^{2 ?}, HCOO^? and CH₃COO^?, a relatively weak acidity is measured: 6.9 μ eq.l^{? 1}. The 40% acid neutralization is explained by the acid gas – alkaline soil particles interaction. The remaining neutralization is from inclusion of gaseous ammonia. When results from Lamto, are compared with those from Banizoumbou (dry savanna) and Zoetele (equatorial forest), a regional view for wet tropospheric chemistry processes is obtained. The high concentration of the particulate phase in precipitation emphasizes the importance of multiphases processes between gases and particles in the atmospheric chemistry of the West Africa ecosystems. For example, the nss Ca^{2 +} precipitation content, main indicator of terrigeneous particles, goes from 30.8 μ eq.l^{? 1} in dry savanna to 9.2 μ eq.l^{? 1} at Lamto and 8.9 μ eq.l^{? 1} in the Cameroon forest. A similar gradient is obtained for rainfall mineral particles precipitation content with contribution of 80% in dry savanna, 40% in wet savanna, and 20% in the equatorial forest.     

Atmospheric Measurements of HONO by Tunable Diode Laser Absorption Spectroscopy

Ambient gas phase nitrous acid (HONO) has been measured by Tunable Diode Laser Absorption Spectroscopy with sub-ppbv detection limits. An R-branch line in the 1263.4 cm^–1 ₃ band was found tobe free of interference and suitable for ambient HONO measurements. Nitrous acid was measured during the night and early morning at an urban site in Toronto, Canada, during the summer of 1998. Average mixing ratios, integrated over 30 minutes, ranged from below the minimum detection limit of 300 pptv to 1.9 ppbv, with the highest concentrations observed during the early morning hours. During the night of 19 June 1998, the concentration of HONO increased by as much as 0.5 ppbv/hr. The usual decrease in HONO after sunrise was delayed by a few hours, possibly due to a combination of an increase in the production rate of HONO with rush hour, and attenuation of the early morning light by high NO₂ within the aerosol fog/haze.     

Short-Term Variability of Atmospheric DMS and Its Oxidation Products at Amsterdam Island during Summer Time

A one-month experiment was performed at Amsterdam Island in January 1998, to investigate the factors controlling the short-term variations of atmospheric dimethylsulfide (DMS) and its oxidation products in the mid-latitudes remote marine atmosphere. High mixing ratios of DMS, sulfur dioxide (SO₂) and dimethylsulfoxide (DMSO) have been observed during this experiment, with mean concentrations of 395 parts per trillion by volume (pptv) (standard deviation, = 285, n = 500), 114 pptv ( = 125, n = 12) and 3 pptv ( = 1.2, n = 167), respectively. Wind speed and direction were identified as the major factors controlling atmospheric DMS levels. Changes in air temperature/air masses origin were found to strongly influence the dimethylsulfoxide (DMSO)/DMS and SO₂/DMS molar ratios, in line with recent laboratory data. Methanesulfonic acid (MSA) and non-sea-salt sulfate (nss-SO₄ ^2–) mean concentrations in aerosols during this experiment were 12.2± 6.5 pptv (1, n=47) and 59 ± 33 pptv (1, n=47), respectively. Evidence of vertical entrainment was reported following frontal passages, with injection of moisture-poor, ozone-rich air. High MSA/ nss-SO₄ ^2– molar ratios (mean 0.44) were calculated during these events. Finally following frontal passages, few spots in condensation nuclei (CN) concentration were also observed.     

The role of pore water in the mechanical behavior of unsaturated soils

Deformation and failure of soils are governed by the stresses acting on the soil skeleton. The isotropic stress acting on the soil skeleton can be divided into two components. One is the stress component which is transmitted through the soil skeleton. This skeleton stress is influenced by the pore water (bulk water) in the soil. The other is the internal stress component which does not contribute to equilibrium with a given external force. The internal stress is induced by the capillary tension of meniscus water clinging to the contact point of soil particles and acts so as to connect the soil particles tightly. Therefore, in modeling the stress and strain relations for unsaturated soils, it is of much importance to quantitatively evaluate how the pore water exists in the soil. This paper discusses the role of pore water on the mechanical behaviour of the soil. In particular, the significance of the water retention curve is emphasized from a mechanical viewpoint. Essential features required in modeling of the constitutive relations for unsaturated soils are discussed and presented.