注入CO2提高煤层气产能的可行性研究

根据煤储层吸附一解吸机理,首次采用“解吸一注气一解吸”的实验方法,分别进行CH4,CO2的吸附一解吸和CO2注入置换煤层CH4实验,模拟了煤层气井“排采一注气一排采”的增产途径和效果。结果表明：在CH4和CO2二元体系的竞争吸附中,CO2组分的吸附速率是先快后慢,而CH4组分的吸附速率先慢后快,解吸时则相反,反映出CO2在竞争吸附中占据优势;注入CO2气体的数量越大和相对浓度越高,单位压降CH4解吸率和CO2吸附率就越高。实验结论对工业规模的煤层气开发试验具有指导意义。     

近地层O3和CO2浓度变化对冬小麦影响的数值模拟：Ⅱ模拟结果和分析

针对CO2和O3浓度变化对冬小麦影响,改进了农田生态系统碳氮生物化学模型(DNDC),并利用模型模拟了O3和CO2浓度变化对冬小麦生长发育和产量的影响,检验了模型的模拟效果.通过对原DNDC模型适用性的调整,使之适用于固城站,为进一步改进作物模型打下了可靠的基础.通过试验资料验证表明,模型较好地反映了O3和CO2浓度变化对冬小麦生长发育和产量形成的影响.通过敏感性分析得出,模型对温度变化反映灵敏;在CO2浓度倍增情况下,O3浓度变化对冬小麦的复合影响分析看出,一定浓度范围内,CO2可缓解O3对作物影响的负效应,O3对CO2带来的正效应有削弱作用.     

The effect of gas-phase chemistry on aqueous-phase sulfur dioxide oxidation rates

The rates and mechanisms of both gas and liquid phase reactions for the oxidation of sulfur dioxide play an important role in the production of atmospheric acids and aerosol particles. Rhodeet al. (1981) concluded that sulfate production rates were highly non-linear functions of sulfur dioxide emission rates. Their modelling study used an HO _x termination mechanism for the HO—SO₂ reaction in the gas-phase. Stockwell and Calvert (1983) determined that one of the products of the overall reaction of HO with sulfur dioxide was an HO₂ radical. The National Research Council (1983) using a version of the Rhodeet al. (1981) model modified to include HO₂ production from the HO—SO₂ reaction concluded that sulfate production becomes much more linear with respect to reductions in sulfur dioxide emissions. However, the cause of this increased linearity was not explained by the National Research Council report. It is demonstrated that the increased linearity is due to the coupling of gas-phases and aqueous phase chemistry. The gas-phase sulfur dioxide oxidation mechanism has a very significant effect on hydrogen perodide production rates.     

Covariations in oceanic dimethyl sulfide,its oxidation products and rain acidity at Amsterdam Island in the Southern Indian Ocean

Simultaneous measurements of rain acidity and dimethyl sulfide (DMS) at the ocean surface and in the atmosphere were performed at Amsterdam Island over a 4 year period. During the last 2 years, measurements of sulfur dioxide (SO₂) in the atmosphere and of methane sulfonic acid (MSA) and non-sea-salt-sulfate (nss-SO₄ ^2-) in rainwater were also performed. Covariations are observed between the oceanic and atmospheric DMS concentrations, atmospheric SO₂ concentrations, wet deposition of MSA, nss-SO₄ ^2-, and rain acidity. A comparable summer to winter ratio of DMS and SO₂ in the atmosphere and MSA in precipitation were also observed. From the chemical composition of precipitation we estimate that DMS oxidation products contribute approximately 40% of the rain acidity. If we consider the acidity in excess, then DMS oxidation products contribute about 55%.     

中国东部橄榄岩包体和榴辉岩中CO_2流体包裹体的碳同位素组成

应用阶段加热技术 ,对中国东部新生代玄武岩中的橄榄岩包体和大别造山带超高压榴辉岩进行了包裹体 CO2 的碳同位素组成测定。结果表明 ,橄榄岩的δ1 3C值变化较大 ,从 - 2 2 .8‰到 0 .7‰ ,明显不同于前人报道的低δ1 3C值 (- 2 8‰～- 2 0‰ )特征 ,指示中国东部地幔流体中 CO2 的碳同位素组成是不均一的 ,反映了地壳有机碳与原生地幔碳的混合特征。大别造山带榴辉岩的 δ1 3C变化从 - 18.5‰到 4 .6‰ ,同样明显不同于前人报道的低 δ1 3C值 (- 30‰～ - 2 0‰ )特征。榴辉岩的低δ1 3C值指示了板块俯冲前其玄武岩原岩受到地表含有机碳流体蚀变后的碳同位素特点 ,而较高的δ1 3C值反映了板块折返过程中榴辉岩受淋滤大理岩的富 CO2 流体叠加的退变质效应。橄榄岩包体和超高压榴辉岩的轻碳同位素共同特点反映了板块俯冲引起的壳—幔物质相互作用和碳同位素地球化学再循环 ,指示中国东部岩石圈地幔含有丰富的地壳有机碳组分     

碳糊电极循环伏安法测定γ－和β－二氧化锰物相

利用碳糊电极循环伏安法对γ－ＭｎＯ＿２和β－ＭｎＯ＿２进行了定量分析，相对于２００．０ｍｇ碳粉的线性范围分别为γ－ＭｎＯ＿２９．１３～４５，６ｍｇ；β－ＭｎＯ＿２４．５６～３６．５ｍｇ，在线性范围内测量７次，其ＲＳＤ分别为０．５９％～５．２８％和Ｏ％～５．７２％。同时对γ－ＭｎＯ＿２和β－ＭｎＯ＿２的混合试样及湘潭电解二氧化锰也进行了定量测定，其平均相对误差分别为２．０１％～１２．４％和１．９６％～７．５２％。该方法进行物相分析，具有简便、快速、灵敏、经济和不经化学分离等特点。     

库伦滴定法测定岩矿试样中氯

本文提出用电生Ag~ 库伦滴定岩矿样品中痕量氯的方法。经对电解液组成、不同电解电流下的电流效率、干扰元素的分离等进行了实验研究,确定了最佳分析条件。实验结果表明:当测定氯量≥100μg时,回收率达99.5～99.9％,相对标准偏差0.33～0.03％;测定氯量≥10μg,回收率为98.6～98.9％;相对标准偏差2.5～0.58%;方法准确,重现性好,操作简便。用岩石和土壤一级标准物质检验及参加建材一级标准物质协作定值,结果满意。     

Inter-annual and seasonal variations in the air–sea CO2 balance in the central Baltic Sea and the Kattegat

We estimated the net annual air–sea exchange of carbon dioxide (CO₂) using monitoring data from the East Gotland Sea, Bornholm Sea, and Kattegat for the 1993–2009 period. Wind speed and the sea surface partial pressure of CO₂ (pCO₂^w), calculated from pH, total alkalinity, temperature, and salinity, were used for the flux calculations. We demonstrate that regions in the central Baltic Sea and the Kattegat alternate between being sinks (−) and sources (+) of CO₂ within the −4.2 to +5.2 mol m⁻² yr⁻¹ range. On average, for the 1994–2008 period, the East Gotland Sea was a source of CO₂ (1.64 mol m⁻² yr⁻¹), the Bornholm Sea was a source (2.34 mol m⁻² yr⁻¹), and the Kattegat was a sink (−1.16 mol m⁻² yr⁻¹). Large inter-annual and regional variations in the air–sea balance were observed. We used two parameterizations for the gas transfer velocity (k) and the choice varied the air–sea exchange by a factor of two. Inter-annual variations in pCO₂^w between summers were controlled by the maximum concentration of phosphate in winter. Inter-annual variations in the CO₂ flux and gas transfer velocity were larger between winters than between summers. This indicates that the inter-annual variability in the total flux was controlled by winter conditions. The large differences between the central Baltic Sea and Kattegat were considered to depend partly on the differences in the mixed layer depth.     

1994-2006年长江三角洲和东北平原酸性气体浓度变化

 利用长江三角洲和东北平原地区大气本底站的二氧化硫（SO2）和氮氧化物（NOx）历史资料和近期取得的观测数据,探讨两个地区人为排放对这些气候相关酸性气体的不同贡献。从两种酸性气体过去和现在的浓度水平,估算了它们在两个地区的增长率,比较了NOx与SO2比值的不同变化趋势。结果表明,早在20世纪90年代中期,长江三角洲酸性气体污染水平已经较高,其后主要是NOx浓度显著升高,从而使该地区成为硫和氮污染并重的地区;东北平原酸性气体过去浓度很低,但这些气体以很高的速率增长,虽然目前浓度水平仍然比较低,但未来形势不容乐观。     

气态SO_2转化及其数值模型研究

本文基于对室外烟雾箱实验,探讨了SO_2的转化机制及影响SO_2转化的因素,由此并借助于烟团模型,建立了SO_2转化和硫酸盐气溶胶细粒子生成的数值模型,用于估算从排放源排入大气的SO_2浓度及其转化成硫酸盐细粒子的浓度以及它们的空间分布,与实测结果相比,两者有较好的一致性.同时指出,由于大气中细粒子(粒径小于1μm)可通过人体呼吸进入并沉积在肺泡中而对健康有不利影响,从而说明研究大气中细粒子污染的迫切性.