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11.
王瑞敏 《岩矿测试》2011,30(3):295-298
样品采用王水溶解,二氯化锡还原,泡沫塑料富集,用Re作内标,电感耦合等离子体质谱法同时测定土壤中超痕量金、铂、钯。在盐酸-二氯化锡体系中,盐酸酸度为15%,二氯化锡浓度为45 g/L,吸附时间30 min时吸附效果明显,吸附温度为25℃时吸附率相对稳定。方法检出限Au为0.21 ng/g,Pt为0.18 ng/g,Pd为0.16ng/g,方法加标回收率Au为91.3%~97.8%,Pt为92.0%~96.7%,Pd为96.0%~101.6%。该方法用于测定国家一级标准物质,线性范围宽、重现性好,结果准确可靠,样品处理简便、快速。  相似文献   
12.
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   
13.
杭健  高若柳 《岩矿测试》2011,30(2):226-229
硫氰酸盐比色法测定钨是基于W5+与硫氰酸盐形成黄色络合物。为使钨完全还原为5价,通常单独使用三氯化钛或氯化亚锡作还原剂。此方法在应用过程中,由于Ti3+本身呈紫色,加多会掩盖络合物的黄色,加少则出现硫氰酸铁之红色丝状物影响比色的情况。通过大量的试验,采用氯化亚锡-三氯化钛作双还原剂,控制最佳酸度、温度和时间,从而获得稳定的络合物,提高了分析结果的稳定性。通过对国家一级标准物质进行分析验证,从而证实方法可行,能够保证样品的测试精密度和准确度。本方法尤其适用于低含量、大批量钨矿样品的测定。  相似文献   
14.
载炭泡塑吸附法对金有良好的吸附性能,但只能用于抽滤吸附不能振荡吸附,分析手续繁杂。本文以载炭泡塑振荡吸附-电感耦合等离子体发射光谱法测定金矿石的金量。样品在650℃高温灼烧2 h,用50%王水和10%氯化铁加热溶解,溶液冷却后加入5%高锰酸钾氧化,用中密度规格的载炭泡塑两次振荡吸附溶液中的金,然后于580℃高温灼烧后以50%王水溶解灰分,直接用ICP-OES测定金量。方法检出限(3σ)为0.002μg/g,精密度(RSD,n=11)小于3.7%。本方法对金的吸附率大于99.9%,测定范围为0.01~90μg/g,对不同类型金矿石的适应性强,解决了以往泡塑吸附法吸附率较低、标准系列与样品需同时预处理的问题,对低含量和高含量样品均有较高的准确度。  相似文献   
15.
珠江三角洲滨海小流域离子化学特征及来源分析   总被引:1,自引:0,他引:1  
在分析中山大学滨海小流域水循环综合试验基地内雨水、河水和地下水离子组分的基础上,讨论了该小流域内水体离子化学组分的特征及来源。结果显示:①河水中TDS变化范围为28.97~44.64 mg/l,平均值为33.90 mg/l;在离子化学组成中,阳离子以Na++K+为主,阴离子以Cl-和HCO3-为主;雨水中TDS的变化范围为0.88~26.07 mg/l,平均值为8.42 mg/l,离子含量变化幅度较大;地下水TDS变化范围为39.49~113.16 mg/l,均值为58.11 mg/l,约为流域河水的2倍,雨水的7倍;②海盐沉降中Ca2+、Mg2+、Na+、K+、SO42-的贡献率:雨季分别为6%、60%、47%、2%和15%,旱季分别为3%、41%、54%、2%、9%;③硅酸盐风化中,雨季:(Ca/Na)sil=0.31,(Mg/K)sil=0.21;旱季:(Ca/Na)sil=0.36,(Mg/K)sil=0.27;CO2消耗率为12.4 t/(km2.a);④河水中的NO3-和(SO42-)res主要来源于大气酸沉降,且具有旱季含量低、雨季含量高的特点;⑤R1潜水井受到一定程度的NO3-污染,NO3-的...  相似文献   
16.
Although Lanzhou is one of the most heavily polluted cities in China, the composition of its air pollutants have not yet been studied in detail. The data of four months on the concentrations and compositions of ions from daily air-filter samples in the winter and spring during 2007–2008 were analyzed to investigate temporal trends and their possible causes. The results indicate that mean concentrations of almost all the aerosol components are greater in winter than in spring due to stronger emissions in winter and weaker localized dispersion. Spring dust storms are the major cause of the highest peak PM10 concentrations recorded during the study period; however, these elevated levels were transient. Ion concentrations related to coal combustion show the greatest reduction from winter to spring, while the concentrations of strong crustal components show a less-pronounced reduction. Strong cycles in the levels of particulate matter (PM) and all ions are also observed during the winter months due to meteorological conditions. Depending on the season, nine different ions accounted for 20%–50% of the PM concentration. The particle size of polluting ions was constant at times of increasing PM concentrations (particularly during winter), whereas the particle size of crustal ions increased dramatically during spring dust storms. Local meteorological conditions (especially wind speed) have a strong influence on the levels of pollutants. Four dust storms were noted, including one during winter. In summary, the regional transport of desert dust from the Gobi can significantly affect air quality and the chemical composition of aerosols in Lanzhou. The dust storms can strongly increase concentration of crustal ions, which are characteristics of deserts in northwestern China. This observation is in agreement with back-trajectories, which show reduced levels of pollutant ions during dust storms. Data on nitrate:sulfate ratios indicate that stationary point sources are the main source of ions rather than mobile sources.  相似文献   
17.
Unlike temperate and polythermal proglacial streams, the proglacial streams in Taylor Valley (TV), Antarctica, are derived primarily from glacier surface melt with no subglacial or groundwater additions. Solute responses to flow reflect only the interaction of glacial meltwater with the valley floor surrounding the stream channel. We have investigated the major, minor and trace element 24‐h variations of two proglacial melt streams, Andersen Creek and Canada Stream, originating from the Canada Glacier in TV, Antarctica. Both streams exhibited diel mid‐austral summer diurnal flow variation, with maximum flow being more than 50 times the minimum flow. Dissolved (< 0.4 µm) major, minor and trace solute behaviors through diel periods were strongly controlled by the availability of readily solubilized material on the valley floor and hyporheic‐biological exchanges. Anderson Creek had generally greater solute concentrations than Canada Stream because of its greater receipt of eolian sediment. Andersen Creek also acquired greater solute concentrations in the rising limb of the hydrograph than the falling limb because of dissolution of eolian material at the surface of the stream channel coupled with minimal hyporheic‐biological exchange. Conversely, Canada Stream had less available eolian sediment, but a greater hyporheic‐biological exchange, which preferentially removed trace and major solutes in the rising limb and released them in the falling limb. Given the dynamic nature of discharge, eolian, and hyporheic‐biological processes, solute loads in TV streams are difficult to predict. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   
18.
Quantifying of direct recharge derived from precipitation is crucial for assessing sustainability of well‐irrigated agriculture. In the North China Plain, the land use is dominated by groundwater‐irrigated farmland where the direct recharge derived from precipitation and irrigation. To characterize the mean rate and historical variance of direct recharge derived from precipitation, unsaturated zone profiles of chloride and δ18O in the dry river bed of the Beiyishui River were employed. The results show that archival time scale of the profile covers the duration from 1980 to 2002 (corresponding to depths from 5 to 2 m) which is indicated by matching the δ18O peaks in the isotope profile with the aridity indexes gained by instrumental records of annual precipitation and annual potential evaporation. Using the chloride mass balance method, the mean rate of the direct recharge corresponding to the archival time scale is estimated to be 3·8 ± 0·8 mm year?1, which accounts for about 0·7% of the long‐term average annual precipitation. Further, the direct recharge rates vary from 2·1 to 6·8 mm year?1 since 1980. Despite the subhumid climate, the estimate of recharge rates is in line with other findings in semiarid regions. The low rate of direct recharge is considered as a result of the relative dry climate in recent decades. In dry river bed, unsaturated zone profiles of chloride and δ18O combined with instrumental records could offer valuable information about the direct recharge derived from precipitation during droughts. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   
19.
Exchange of groundwater and lake water with typically quite different chemical composition is an important driver for biogeochemical processes at the groundwater‐lake interface, which can affect the water quality of lakes. This is of particular relevance in mine lakes where anoxic and slightly acidic groundwater mixes with oxic and acidic lake water (pH < 3). To identify links between groundwater‐lake exchange rates and acid neutralization processes in the sediments, exchange rates were quantified and related to pore‐water pH, sulfate and iron concentrations as well as sulfate reduction rates within the sediment. Seepage rates measured with seepage meters (?2.5 to 5.8 L m‐2 d‐1) were in reasonable agreement with rates inverted from modeled chloride profiles (?1.8 to 8.1 L m‐2 d‐1). Large‐scale exchange patterns were defined by the (hydro)geologic setting but superimposed by smaller scale variations caused by variability in sediment texture. Sites characterized by groundwater upwelling (flow into the lake) and sites where flow alternated between upwelling and downwelling were identified. Observed chloride profiles at the alternating sites reflected the transient flow regime. Seepage direction, as well as seepage rate, were found to influence pH, sulfate and iron profiles and the associated sulfate reduction rates. Under alternating conditions proton‐consuming processes, for example, sulfate reduction, were slowed. In the uppermost layer of the sediment (max. 5 cm), sulfate reduction rates were significantly higher at upwelling (>330 nmol g‐1 d‐1) compared to alternating sites (<220 nmol g‐1 d‐1). Although differences in sulfate reduction rates could not be explained solely by different flux rates, they were clearly related to the prevailing groundwater‐lake exchange patterns and the associated pH conditions. Our findings strongly suggest that groundwater‐lake exchange has significant effects on the biogeochemical processes that are coupled to sulfate reduction such as acidity retention and precipitation of iron sulfides. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   
20.
Influence of core property on multi-electron process in the collisions of q=6-9 and 11 isocharged sequence ions with Ne is investigated in the keV/u region. The cross-section ratios of double-, triple-, quadruple- and total multi-electron processes to the single electron capture process as well as the partial ratios of different reaction channels to the relevant multi-electron process are measured by using position-sensitive and time-of-flight techniques. The experimental data are compared with the theoretical predictions including the extended classical over-barrier model, the molecular Columbic barrier model and the semi-empirical scaling law. Results show a core effect on multi-electron process of isocharge ions colliding with Neon, which is consistent with the results of Helium we obtained previously.  相似文献   
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