首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   621篇
  免费   169篇
  国内免费   330篇
测绘学   11篇
大气科学   44篇
地球物理   123篇
地质学   689篇
海洋学   109篇
天文学   17篇
综合类   27篇
自然地理   100篇
  2024年   18篇
  2023年   30篇
  2022年   37篇
  2021年   54篇
  2020年   33篇
  2019年   62篇
  2018年   25篇
  2017年   22篇
  2016年   24篇
  2015年   32篇
  2014年   64篇
  2013年   32篇
  2012年   31篇
  2011年   40篇
  2010年   42篇
  2009年   37篇
  2008年   40篇
  2007年   32篇
  2006年   63篇
  2005年   55篇
  2004年   41篇
  2003年   33篇
  2002年   24篇
  2001年   21篇
  2000年   32篇
  1999年   29篇
  1998年   35篇
  1997年   25篇
  1996年   17篇
  1995年   9篇
  1994年   19篇
  1993年   11篇
  1992年   9篇
  1991年   12篇
  1990年   5篇
  1989年   5篇
  1988年   8篇
  1987年   4篇
  1986年   1篇
  1985年   1篇
  1984年   2篇
  1982年   1篇
  1980年   1篇
  1978年   2篇
排序方式: 共有1120条查询结果,搜索用时 668 毫秒
161.
为了深入认识库米什盆地硝酸盐矿床成矿离子的空间分布特征、表层沉积物中硝酸盐含量较高的原因,以盆地硝酸盐矿床为研究对象,开展研究区内各类补给水样和沉积物样可溶性盐类物质化学组成的定量分析研究;结合野外地质踏勘工作,探讨研究区硝酸盐矿床成矿离子的迁移规律,初步建立盆地硝酸盐矿床沉积成矿作用模型.结果表明,K+、Na+、NO...  相似文献   
162.
中国华南吉泰盆地在白垩纪?古近纪发育大量蒸发岩,其中含富锂卤水矿床,由于盆地深部构造特征认识不清,导致富锂卤水矿勘查评价明显滞后.基于盆地东北部泰和坳陷二维地震数据和钻孔资料,经过精细保幅处理和综合构造解释,总结了含富锂卤水矿断陷盆地的深部构造特征.地震剖面和构造属性表明,盆地深部发育错断白垩系的NE-SW走向、NW倾...  相似文献   
163.
离子色谱法检测土壤样品水溶态中的七种阴离子   总被引:3,自引:0,他引:3  
采用离子色谱法测定土壤样品水溶态中的F^-、Cl^-、NO2^-、SO4^2-、Br^-、NO3^-、PO4^3-。通过优化提取条件,得出最优条件下7种阴离子的加标回收率为94.4%~102.5%,精密度为3.1%~4.6%。对实际样品进行测试,结果表明,该方法适用于土壤样品水溶态中7种阴离子的定性、定量分析。  相似文献   
164.
阐述了全站仪在日常工作中使用、保管以及全站仪电池充放电的注意事项。  相似文献   
165.
复方化学消毒剂中苯扎氯铵的高效液相色谱测定   总被引:1,自引:0,他引:1  
建立了一种测定复方化学消毒剂中苯扎氯铵成分十二烷基二甲基苄基氯化铵、十四烷基二甲基苄基氯化铵和十六烷基二甲基苄基氯化铵的反相离子对高效液相色谱法。色谱柱为Platisil ODS(5μm,250 mm×4.6mm),流动相为甲醇-0.2 mol/L己烷磺酸钠(含1%三乙胺,V/V,用高氯酸调节至pH=6.0,体积比85∶15),紫外220 nm检测。用己烷磺酸钠作为离子对试剂,增强了苯扎氯铵成分的保留,三乙胺作为扫尾剂,通过抑制固定相表面残存的硅羟基对苯扎氯铵成分的吸附,减少了色谱峰拖尾。3种苯扎氯铵成分分离良好,标准曲线的线性范围分别为0.002~5 mg/mL、0.005~10 mg/mL和0.005~10 mg/mL,检测限分别为0.0005 mg/mL、0.001mg/mL和0.001 mg/mL。方法具有良好的准确度和精密度,在测定低浓度样品时优势明显。实际用于测定苯扎氯铵消毒液和医用消毒纸巾中3种苯扎氯铵成分的含量,回收率为99.3%~104.1%,日内和日间测定相对标准偏差(RSD)均小于2.0%。  相似文献   
166.
In order to discuss the role and influence of water during the generation of natural gas, the participation mechanism of water during the evolution of organic matter and its influences were summarized. In addition, we carried out an anhydrous cracking experiment of oil extracted from the Feixianguan Formation source rock in a closed system, which led to the establishment of the kinetic models for describing carbon and hydrogen isotopic fractionation during gas generation from organic matter. The models were calibrated and then applied to the northeastern Sichuan Basin. By combining a series of gas generation experiments from octadecane pyrolysis without water or with distilled water in varying mass proportions, several results were proved: (1) the hydrogen isotopic composition of natural gas becomes lighter with the participation of formation water; (2) we can quantitatively study the hydrogen isotopic fractionation with the kinetic model for describing carbon isotopic fractionation; (3) more abundant and reliable geological information can be obtained through the combined application of carbon and hydrogen isotopic indices.  相似文献   
167.
摘 要:利用连续一年旌德县负氧离子监测数据,分别以兔儿山公园、路西村茶园代表城市公园、高山茶园这两种生态环境,对城市公园和高山茶园负氧离子浓度特征以及气象要素对负氧离子浓度影响进行比较分析。结果表明:①高山茶园负氧离子浓度显著高于城市公园;②负氧离子浓度夏季最高,冬季最低,春秋季次之,6月负氧离子浓度达全年最高;③负氧离子浓度日变化整体呈“一峰一谷”变化趋势,峰值出现在上午,谷值出现在正午前后,夜间至上午负氧离子浓度较高,城市公园负氧离子浓度日较差较高山茶园偏小;④负氧离子浓度日变化与气温、风速呈显著负相关;⑤负氧离子浓度雨天最高,晴天次之,阴天和多云相对较低,暴雨天气条件下大气负氧离子浓度显著提高。  相似文献   
168.
A petrographic investigation revealed polyphase quartz cementation in the Finefrau Sandstone (Upper Carboniferous, Western Germany) and the Solling Sandstone (Lower Triassic, Central Germany). Three different cements could be distinguished in each sandstone based on their cathodoluminescence and trace element composition. The first quartz generation is suggested to have been formed during eogenesis due to dissolution and replacement of feldspar. The mesogenetic paragenesis comprises two generations of quartz and illite, which are accompanied by albite in the Solling Sandstone. Sharp luminescence zoning in quartz overgrowths points to distinct episodes of cementation in both sandstones. Significant amounts of Al, Li and H and traces of Ge and B have been detected in the quartz overgrowths. The Al‐content of the quartz cements in the Finefrau Sandstones exceeds that in the quartz cements in the Solling Sandstone by a factor of five. It is suggested that this compositional variation reflects the conditions in the pore‐water, such as temperature and pH. The Al‐concentration is generally correlated to the Li‐content with the exception of the latest quartz generation in the Finefrau Sandstones which is also most enriched in trace elements. The ratio of Li/Al varies between 0·11 and 0·25 in the two sandstones. The Li/H‐ratio, which ranges from 0·12 to 0·3, is controlled by the activity ratio of Li and H in the pore fluid. Clay minerals are the most important source for Li and high salinities favour the mobilization of Li during diagenesis. Thus, a relatively low salinity and low pH are responsible for the low Li/H‐ratio in the Finefrau Sandstone, while high salinity and neutral to alkaline pH results in a high Li/H‐ratio for the Solling Sandstone. The Ge‐contents are generally near the average of detrital quartz and indicate that pressure dissolution is a major source for quartz cementation. Different chemical compositions of distinct quartz generations indicate changes in the physico‐chemical conditions and point to mobilization of silica from different sources (for example, pressure solution and clay mineral transformations).  相似文献   
169.
传统的Fenton均相亚铁盐催化剂处理染料废水,具有难以避免的二次污染和亚铁离子流失问题。分子筛催化剂相比传统催化剂具有高效环保的特点,在催化氧化染料废水领域有着良好的前景。本文通过液相离子交换法制备了Fe-ZSM-5非均相分子筛催化剂,替代传统的亚铁盐催化剂,应用X射线衍射对制备的Fe-ZSM-5分子筛催化剂进行表征,表明随离子交换次数的增加,Fe-ZSM-5催化剂负载的铁量上升,且较好地保持了分子筛结构,有利于提高亚铁离子的催化能力。通过实验确定了Fe-ZSM-5催化剂催化反应的最佳温度、pH值、Fe-ZSM-5的用量、反应时间等工艺参数,比较了Fe-ZSM-5催化剂和传统Fenton均相催化剂降解染料废水的脱色率和废水中铁离子的残留量,结果表明Fe-ZSM-5的脱色率达到98.5%,相比于Fenton均相催化剂的脱色率提升约3%;两种催化剂的铁离子残留量差别显著,Fe-ZSM-5催化剂处理的废水中只产生微量的Fe离子,可以认为Fe-ZSM-5非均相分子筛催化剂有效地解决了催化剂损耗和二次污染问题。  相似文献   
170.
A new method for the simultaneous recovery of U, Th and Pb from ca. 0.5 g calcium carbonate samples for the purpose of U‐(Th)‐Pb geochronometry is presented. The protocol employs ion‐exchange chromatography. Standard anion exchange resin (AG 1‐X8 100–200 mesh) was used as the static phase, and 90% acetic acid was used as the mobile phase to elute the unwanted matrix components; dilute nitric acid was used to elute the U, Th and Pb. Blanks of 1.8 pg Th, 6.4 pg Pb and 8.4 pg U were obtained. The protocol was evaluated by determining the isotopic composition of U‐Th‐Pb separates obtained from an in‐house reference material (prepared from a natural speleothem) by MC‐ICP‐MS. An independently dated speleothem was also reanalysed. Based on these tests, the extraction protocol had an acceptable blank and produced a Pb separate sufficiently free of matrix‐induced instrumental biases to be appropriate for U‐Th‐Pb chronology.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号