国内外钼资源供需形势分析

全面、系统地建立钼矿石、钼矿粉分析方法,对钼元素研究开发和保障钼矿工业发展具有重要意义。目前多采用酸溶或碱熔样品后进行分析,其不足是测定钼含量的范围窄,消耗样品量大,还需使用大量酸碱,且受仪器限制,分析高含量钼时多需对样品溶液进行数次稀释,使分析步骤更加繁琐。发射光谱法则可避免上述问题,但用之准确分析高含量钼矿石钼矿粉尚有测试方法的瓶颈需要突破。本文研究通过内标元素、分析线对、缓冲剂配比、电流程序等环节的实验分析,建立了固体进样-交流电弧发射光谱法测定钼矿石中高含量钼的分析方法：优化样品与光谱缓冲剂质量比至1∶2,优化分析线对,截取曝光时间35s,采用以国家一级合成硅酸盐光谱分析标准物质和国家一级矿石标准物质组成的自研标准系列制作标准曲线,由全谱交直流电弧发射光谱仪自动扣除分析线和内标线背景后以对数坐标二次曲线拟合计算,使测定范围扩展为500～500800μg/g,检出限为27.38μg/g,相对标准偏差（RSD）为3.28%～8.30%,相对误差为-0.43%～0.73%。结果表明,本文方法在实现绿色分析的同时,在检出限相当、精密度合格的条件下,一次性分析高含量钼的上限从5%提高至50%。

     

兰州不同时期黄土有机质碳同位素与气候的关系

基于兰州九州台黄土剖面的土壤有机质δ13C分析,讨论了兰州地区末次间冰期和全新世2个时期气候以及地表植被的变化特征.结果表明,该地区末次间冰期δ13C变化范围为-29.97‰～-25.52‰,平均值为-27.79‰;全新世δ13C变化范围在-20.82～-34.40‰之间,平均值为-28.99‰.从δ13C平均值来看,该地区在以上两个时期地表植被主要为C3植物.末次间冰期九州台剖面δ13C表现出3峰夹2谷的特征与同一时期深海SPECMAP曲线有着良好的对应,表明了该时期兰州地区的气候变化与全球是一致的,全新世土壤有机质δ13C所反映出的3个不同的变化阶段对应于早、中、晚全新世阶段.结合黄土高原其他剖面相应时期的土壤有机质δ13C的研究结果,我们观察到陕西关中地区的黄土剖面末次间冰期和全新世土壤有机质δ13C要大于黄土高原西部的兰州等地区,气候差异引起的地表植被中C3、C4植物比例不同是造成两地区土壤有机质δ13C差异的主要因素.研究结果表明,黄土高原土壤有机质δ13C是揭示该地区气候变化的一个良好代用指标.     

大气中一氧化碳浓度变化的模拟研究

应用全球二维大气化学模式,模拟了CO、CH4和OH自由基等成分自工业革命到2020年的长期变化.模拟的全球CO平均体积分数在1840年、1991年和2020年分别为27×10-6、76×10-6和105×10-6.从1840到1991年,OH自由基数浓度从7.17×105个分子/cm3下降到5.79×105个分子/cm3,降低了19%.模拟的CH4长期变化与冰芯资料相符.模拟的20世纪80年代CO体积分数年增长率为1.03%～1.06%.大气中CO在20世纪90年代前是增长的,而到90年代初观测到CO体积分数突然下降.应用二维大气化学模式对此原因进行了模拟研究,结果表明,CO排放源的减少是CO体积分数下降的主要因子,平流层臭氧减少是另一个重要因子.尽管CO排放源的减少对大气CH4增长率的变化有较大影响,而CH4排放源减少对CO体积分数变化却几乎没有影响.     

风蚀作用下的土壤碳库变化及在中国的初步估算

土壤有机碳库储量巨大且在表层富集 ,而风力侵蚀具有巨大的卷挟起沙、搬移输运和空间再分配能力 ,对土壤有机碳库的演变具有重要影响。在风力侵蚀作用下 ,风蚀发生地、风蚀土壤输运途中以及风蚀土壤沉降地的土壤有机碳库有着不同的变化过程。基于质量平衡原理 ,可以建立土壤有机碳流失及各路径碳输移量估算的模型。依据第二次全国遥感侵蚀调查以及第二次全国土壤普查数据 ,在GIS支持下 ,分析了中国土壤有机碳库以及风力侵蚀的空间格局 ,并计算得到风力侵蚀作用下中国土壤有机碳库储量变化以及各路径碳输移量。研究表明 ,我国因风力侵蚀造成的土壤有机碳流失量约为 5 9 76× 10 6 tC/yr,风蚀所致CO2 排放约为 2 9 88× 10 6 tC/yr;风蚀所致的土壤有机碳流失主要发生在中国西北部的干旱半干旱的农区和牧区     

河流-河口-近海连续体碳循环研究进展

河流-河口-近海连续体(简称连续体)是连接陆地和大洋的过渡地带,也是目前全球碳收支估算的薄弱环节.这个复杂的海陆交互生态系统不仅可以通过光合作用、溶解作用吸收大气中的CO2,陆地和流域光合作用或化学风化作用固定的碳也可以被横向输送到陆架和大洋中.本文以国际上著名的切萨皮克湾以及长江-长江口-东海等为例,综述了连续体碳循...     

高压密闭消解-电感耦合等离子体光谱和质谱联合测定海洋地质样品中52种元素

An improved analytical method to determine the content of 52 major, minor and trace elements in marine geological samples, using a HF-HCl-HNO_3 acid system with a high-pressure closed digestion method(HPCD), is studied by an inductively coupled plasma optical emission spectrometry(ICP-OES) and an inductively coupled plasma mass spectrometry(ICP-MS). The operating parameters of the instruments are optimized, and the optimal analytical parameters are determined. The influences of optical spectrum and mass spectrum interferences, digestion methods and acid systems on the analytical results are investigated. The optimal spectral lines and isotopes are chosen, and internal standard element of rhodium is selected to compensate for matrix effects and analytical signals drifting. Compared with the methods of an electric heating plate digestion and a microwave digestion, a high-pressure closed digestion method is optimized with less acid, complete digestion,less damage for digestion process. The marine geological samples are dissolved completely by a HF-HCl-HNO_3 system, the relative error(RE) for the analytical results are all less than 6.0%. The method detection limits are 2–40μg/g by the ICP-OES, and 6–80 ng/g by ICP-MS. The methods are used to determine the marine sediment reference materials(GBW07309, GBW07311, GBW07313), rock reference materials(GBW07103, GBW07104,GBW07105), and cobalt-rich crust reference materials(GBW07337, GBW07338, GBW07339), the obtained analytical results are in agreement with the certified values, and both of the relative standard deviation(RSD) and the relative error(RE) are less than 6.0%. The analytical method meets the requirements for determining 52 elements contents of bulk marine geological samples.     

Geomechanical modelling to assess fault integrity at the CO2CRC Otway Project,Australia

This paper presents the first published 3D geomechanical modelling study of the CO2CRC Otway Project, located in the state of Victoria, Australia. The results of this work contribute to one of the main objectives of the CO2CRC, which is to demonstrate the feasibility of CO₂ storage in a depleted gas reservoir. With this aim in mind, a one-way coupled flow and geomechanics model is presented, with the capability of predicting changes to the in situ stress field caused by changes in reservoir pressure owing to CO₂ production and injection. A parametric study investigating the pore pressures required to reactivate key, reservoir-bounding faults has been conducted, and the results from the numerical simulation and analytical analysis are compared. The numerical simulation indicates that the critical pore fluid pressure to cause fault reactivation is 1.15 times the original pressure as opposed to 1.5 times for the comparable analytical model. Possible reasons for the differences between the numerical and analytical models can be ascribed to the higher degree of complexity incorporated in the numerical model. Heterogeneity in terms of lateral variations of hydrological and mechanical parameters, effect of topography, presence of faults and interaction between cells are considered to be the main sources for the different estimation of critical pore pressure. The numerical model, which incorporates this greater complexity, is able then to better describe the state of stress that acts in the subsurface compared with a simple 1D analytical model. Moreover, the reactivation pressures depend mainly on the state of stress described; therefore we suggest that numerical models be performed when possible.     

Experimental study on soil CO2 emission in the alpine grassland ecosystem on Tibetan Plateau

The Tibetan Plateau, the Roof of the World, is the highest plateau with a mean elevation of 4000 m. It is characterized by high levels of solar radiation, low air temperature and low air pressure compared to other regions around the world. The alpine grassland, a typical ecosystem in the Tibetan Plateau, is distributed across regions over the elevation of 4500 m. Few studies for carbon flux in alpine grassland on the Tibetan Plateau were conducted due to rigorous natural conditions. A study of soil respiration under alpine grassland ecosystem on the Tibetan Plateau from October 1999 to October 2001 was conducted at Pangkog County, Tibetan Plateau (31.23°N, 90.01°E, elevation 4800 m). The measurements were taken using a static closed chamber technique, usually every two weeks during the summer and at other times at monthly intervals. The obvious diurnal variation of CO2 emissions from soil with higher emission during daytime and lower emission during nighttime was discovered. Diurnal CO2 flux fluctuated from minimum at 05:00 to maximum at 14:00 in local time. Seasonal CO2 fluxes increased in summer and decreased in winter, representing a great variation of seasonal soil respiration. The mean soil CO2 fluxes in the alpine grassland ecosystem were 21.39 mgCO2 · m-2 · h-1, with an average annual amount of soil respiration of 187.46 gCO2 · m-2 · a-1. Net ecosystem productivity is also estimated, which indicated that the alpine grassland ecosystem is a carbon sink.     

贵州百花湖分层晚期有机质降解过程与溶解N2O循环

百花湖是一个具有季节性分层的富营养小型湖泊,在秋季湖水倒转期经常发生水质恶化事件,碳氮循环出现异常。文章研究特选择在秋初,湖泊分层开始消失时,测定了湖水中不同深度的N₂O,CH₄,CO₂,有机和无机碳同位素以及其他化学参数变化。结果发现:采样时百花湖在约6m和16m深度附近出现了两个温度不连续层(SDL和PDL),并影响到有机颗粒的沉降和分解。相对而言,有较多的有机质在这两个层内发生降解,但降解的途径有所不同,上部主要是有氧降解,下部则主要是无氧降解过程。N₂O的产生和消耗与有机质的降解过程完全对应:PDL层以上,ΔN₂O与AOU的线性关系反映了N₂O主要形成于硝化作用;PDL层以下反硝化作用导致N₂O严重不饱和;PDL内位于硝化作用和反硝化作用过渡带的N₂O峰,显然是硝化与反硝化联合作用的结果。PDL层内较大的CH₄浓度变化梯度,说明嗜甲烷细菌可能通过氧化NH+4贡献了部分N₂O。百花湖秋、冬季表层湖水N₂O都是过饱和的,都是大气N₂O的源,依据分子扩散模型计算湖泊N₂O的释放通量在12～14μmol/m·day之间,秋、冬季没有明显的差别。秋季底层湖水的反硝化作用是湖泊N₂O的汇,其消耗通量与表层的释放通量基本相当。     

有机化学物质碳氮稳定同位素系列标准物质研制

实验室和研究人员所使用的碳、氮同位素标准物质一般由国际原子能机构(IAEA)获得,然而近年来,随着碳氮同位素在实验室质量监控、方法评价、仪器校准等方面的广泛应用,市场需求量不断增加, IAEA研制的碳、氮同位素标准物质的种类与数量逐渐不能满足科学研究快速发展的需求。我国急需研制适应当今分析技术水平的有机质碳氮同位素国家标准物质用以进行质量监控、方法评价、仪器校准。为保证量值传递精度,本文研制了4个有机化学物质的碳氮稳定同位素标准物质,其中3个为尿素样品,1个为L-谷氨酸。经检验4种标准物质的均匀性通过F值检验,标准物质的δ~(13)C和δ~(15)N值经过一年的稳定性检验,特征量值变化在测量方法允许的不确定度范围内,由此判定δ~(13)C和δ~(15)N值稳定性良好。由包括研制单位实验室在内的12家实验室协同定值,采用高温燃烧-气体同位素质谱法测定了δ~(13)C和δ~(15)N值,系列标准物质δ~(13)C和δ~(15)N认定值区间呈梯度分布,δ~(13)C值为-40‰～0‰,δ~(15)N值为-10‰～30‰,涵盖了我国天然样品中有机质碳氮稳定同位素组成范围;研制的系列标准物质δ~(13)C的定值扩展不确定度不大于0.08‰,δ~(15)N的定值扩展不确定度不大于0.09‰,定值水平与国际标准物质相当。该系列标准物质已被国家质检总局批准为国家一级标准物质,批准号为GBW04494～GBW04497。可被用于地质、生态、环境等多种样品δ~(13)C和δ~(15)N比值测定时的分析监控、仪器校准、方法评价、质量保证和质量监控。