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1.
刘道飞  陈圣波  路鹏 《地球学报》2015,36(2):245-249
为了研究利用Clementine热红外数据反演月球表面岩石的氧化钙(Ca O)含量,论文选取了两景覆盖Apollo17登月点的Clementine热红外影像,将其覆盖的区域选为研究区。利用月球表面温度物理模型模拟月表温度,结合普朗克函数,完成发射率反演。在此基础上,对LPI中35个除Apollo17登月计划外所采集的样品Ca O含量与其热红外发射率特征做回归统计分析,发现存在很好的线性关系(R2=0.661)。由此,基于Clementine热红外发射率实现了研究区Ca O含量反演。通过利用LPI Apollo17月岩(壤)样品实际Ca O含量分析数据对反演结果进行精度评价,发现8组反演值与实际值的相对误差最小为1.77%,最大为9.29%,均方根误差为0.767。研究结果表明,使用发射率进行Ca O含量反演方法可行,为利用Clementine热红外数据对月表矿物成分含量定量反演提供一种新的思路。  相似文献   
2.
张维萍  赫英  董振信 《地球化学》2007,36(4):419-424
采集中国北方玄武岩中橄榄岩包体样品21件。测定了其中的主元素、微量元素、稀土元素(REE)和Au等的含量。橄榄岩包体中的Au含量与CaO含量的相关性表明,其中的Au可能主要赋存于单斜辉石中,反映Au含量可能与地幔演化及熔融程度有关;橄榄岩包体后期受地幔流体交代作用的影响,Au转而以硫化物形式存在,这一过程是在橄榄岩包体原有Au的物质基础上进行的。  相似文献   
3.
The Xining Basin,located on northeastern Qinghai-Xizang Plateau,is adjacent to the Qaidam Bsim and Gobi-desert.Therefore,thick,integrated deposits of loess or paleo-sol sequence were well developed.As is well known,there is much paleo-environmental information recorded in loess and plaeo-sol.So if we deal with paleo-environmental index from different an gles ,especially from loess geochemistry,some important and detailed paleo-environmental evolutional information will be acquired.Based on this,the authors determined the contents of Sr and Ca contained in acid-soluble fraction from the bottom to the top of the Panzishan section.This section was obtained through making a well about 17 m in depth,including S1 paleo-sol that was developed during the last interglacial period.According to the results,it is found that variations in contents of Sr and Ca are well correlated with conversion of loess and paleo-sol.In loess deposits,the contents of Sr and Ca are higher than those in paleo-sol deposits.It is known that loess was deposited under cold-dry climate conditions and paleo-sol was developed during warm-humid climate episodes.It is concluded that due to their mobile behaviors,under cold-dry climate conditions,Sr and Ca are stagnant during weak weathering,but under warm-humid climate conditions,Sr and Ca are easily leached and transported in aqueous solution.Therefore,they can be utilized as indicatiors of climate changes.Moreover,variations in contents of Sr and Ca are more sensitive than susceptibility.The mobile behaviors of Sr and Ca contained in acid-soluble fraction can serve as a new quantitative index to evaluate paleo-environmental changes on the plateau.  相似文献   
4.
Using density functional simulations, within the generalized gradient approximation and projector-augmented wave method, we study structures and energetics of CaSiO3 perovskite in the pressure range of the Earths lower mantle (0–150 GPa). At zero Kelvin temperature the cubic CaSiO3 perovskite structure is unstable in the whole pressure range, at low pressures the orthorhombic (Pnam) structure is preferred. At 14.2 GPa there is a phase transition to the tetragonal (I4/mcm) phase. The CaIrO3-type structure is not stable for CaSiO3. Our results also rule out the possibility of decomposition into oxides.
Daniel Y. JungEmail: Phone: +41-44-6323744Fax: +41-44-6321133
  相似文献   
5.
以盐湖副产水氯镁石为原料,与一定比例的石灰反应得到氢氧化镁和氢氧化钙的混合沉淀物,该混合物经过滤、洗涤、烘干后在一定温度下煅烧得到符合皮江法炼镁用的合成煅白。实验结果表明,该工艺是可行的,在石灰/氯化镁摩尔比2.05~2.10:1,反应时间1.5,煅烧温度为800℃,煅烧时间为60min时,合成的煅白中钙镁摩尔比: 0.95~1.07:1,煅白的平均水活度达34%,符合硅热法炼镁用中间原料煅白的参数条件。该技术可为利用盐湖氯化镁制备金属镁新工艺开发提供了数据参考。  相似文献   
6.
针对温州某钻孔灌注桩废弃泥浆进行了沉降柱试验和颗粒分析实验,研究有机絮凝剂APAM以及无机絮凝剂CaO对泥浆沉降性能和颗粒粒径的影响,着重探究了无机絮凝剂CaO的不同添加顺序对有机絮凝剂APAM絮凝效果的影响。结果表明:在较少APAM添加量(10 mL)下后添加CaO能增大泥浆的初始沉降量;先添加CaO再添加APAM,不利于APAM絮凝作用的发挥;后添加CaO的情况下,CaO对于最终的絮体粒径的影响主要取决于絮体本身的强度及搅拌强度。  相似文献   
7.
田建平  戈润滔  华磊 《云南地质》2011,30(2):204-207
采用2.5次微分催化极谱法,在硫酸—硫酸羟胺—硫酸钠—抗坏血酸—碲(Ⅳ)混合底液中,在国产JP3-1型极谱仪上,于起始电位-0.700伏,终止电位-1.200伏,测定矿石中微量铼。铼浓度在0—15μg/25m l可保持线性关系,且灵敏度高,重现性好,完全满足钼矿、辉钼矿中,以及其他矿物中微量铼的测定。  相似文献   
8.
The Boteti palaeo‐estuary in northern Botswana is located where the endoreic Boteti river, an overflow from the regional Okavango river system, enters the Makgadikgadi pans. The present work considers diagenetic silica and calcium carbonate dominated transformations. The aims are to help identify precursor conditions for the origin of microcrystalline silcrete–calcrete intergrade deposits while developing insight into pene‐contemporaneous silica and calcite matrix formation. General precursor conditions require the presence of cyclical endoreic freshwater inflow into a saline pan. The pan should be deep enough to sustain a permanent watertable under climatic conditions sufficient to cause carbonate fractionation within the groundwater. Freshwater inflow into a saline pan drives the geochemistry of the system (from freshwater to saline, from neutral to high pH). The geochemistry is controlled by the periodicity of inflow relative to salinity levels of phreatic groundwater in the receptor saline pan. The source of most silica and localized CaCO3 is derived from the dissolution and precipitation of micro‐fossils, while more general CaCO3 enrichment stems from saline pan based carbonate fractionation. Diagenetic change leads to colloidal then more consolidated bSiO2/CaO aggregate formation (amorphous silica) followed by transformations into opaline silica over time. Irregular zones of siliceous sediment forming in otherwise calcareous deposits may relate to the irregular occurrence of biogenic silica in the source sediments, inferring a source for local silica mobilization in intergrade deposits. The distribution of calcareous micro‐fossils may have a similar converse effect. Diagenetic evidence from an intergrade deposit with a low SiO2/CaO ratio suggests that transformation occurred more into the pan, while an intergrade deposit with a high SiO2/CaO ratio more likely formed closer to a land margin and was frequently inundated by freshwater. Pene‐contemporaneous silcrete–calcrete intergrade formation under the above conditions may take place where dissolved silica crystallizes out in the vicinity of calcite crystals due to local decreases in pH. The continuing consolidation of bSiO2/CaO aggregates may be facilitated by the presence of increasing amounts of calcite. It appears that CaCO3 may act as a catalyst leading to pene‐contemporaneous bSiO2/CaO aggregate formation. However the processes involved require further work. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   
9.
本实验采用湿法消解碳酸盐岩矿石样品,利用电感耦合等离子体发射光谱仪(ICP-AES),采用内标法和基体匹配法相结合测定了碳酸盐岩标准物质(GBW10035a)中高达54%的氧化钙主量元素含量及其它常微量元素的含量;对实际样品中微量元素进行样品加标回收率实验,对主量和常量元素采用稀释法验证。实验结果表明,样品加标回收率在94%~108%之间,稀释比率在99.4%~100.2%,标准物质测定值与标准值吻合,6次平行样测定的稳定性4%;该方法一次溶样,径向测定主量和常量元素,轴向测定微量元素含量,操作简单,快速,该方法适用于盐湖碳酸盐样品,以及其他含有碳酸盐的各类样品的分析测试。  相似文献   
10.
地球早期生命起源的第一步是合成简单的有机化合物,但合成有机物所需能量来源问题长期困扰着学术界。早期地球上丰富的硫化物半导体矿物可将太阳光子转化为光电子,提供持续的能量来源。也正是由于矿物光电子能量较高,在非生物途径合成小分子有机物方面具有优势。其中半导体矿物自然硫转化太阳能产生的光电子能量,是目前所发现的最高的矿物光电子能量,不仅能直接还原CO2分子为甲酸物质,还可催化其他生命基础物质的合成。在全球陆地系统中暴露在阳光下的岩石/土壤表面普遍被一层铁锰氧化物“矿物膜”所覆盖,光照下含半导体矿物水钠锰矿的“矿物膜”产生原位、灵敏、长效的光电流,显示出优异的光电效应。生物光合作用中心Mn4CaO5在裂解水产氧过程中产生成分和结构类似水钠锰矿的结构中间体,地球早期“矿物膜”中水钠锰矿可能促进了锰簇Mn4CaO5与生物光合作用的起源与进化。早期地球半导体矿物为生命起源基本物质的合成提供直接能量来源,矿物光电子能量在地球早期生命起源与进化中起到了重要作用。  相似文献   
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