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51.
52.
A two-dimensional equation governing the steady state spatial concentration distribution of a reactive constituent within a heterogeneous advective–dispersive flow field is solved analytically. The solution which is developed for the case of a single point source can be generalized to represent analogous situations with any number of separate point sources. A limiting case of special interest has a line source of constant concentration spanning the domain’s upstream boundary. The work has relevance for improving understanding of reactive transport within various kinds of advection-dominated natural or engineered environments including rivers and streams, and bioreactors such as treatment wetlands. Simulations are used to examine quantitatively the impact that transverse dispersion (deviations from purely stochastic-convective flow) can have on mean concentration decline in the direction of flow. Results support the contention that transverse mixing serves to enhance the overall rate of reaction in such systems.  相似文献   
53.
Hydrothermal systems are characterised by complex interactions between heat transfer, fluid flow, deformation, species transport and chemical reactions. Numerical models can provide quantitatively constrained information in regions where acquisition of new data is difficult or expensive thus providing a means for reducing risks, costs, and effort during targeting, production, and management of resources linked to hydrothermal systems. Here we show how numerical simulations of hydrothermal processes can be used to better understand coupled reactive transport in modern geothermal systems and in ancient hydrothermal ore deposits. We give examples based on the Enhanced Geothermal System at Soultz-sous-Forêts in France, hydrothermal mineralisation at Mount Isa in Australia, and the geothermal resource at Hamburg-Allermöhe in Germany.  相似文献   
54.
Nymphaea rubra stem was used as a low cost and easily available biosorbent for the removal of Reactive Red 2 dye from an aqueous solution. Initially, the effects of biosorbent dosage (0.2–1.0 g L–1), pH (1–6), and dye concentration (30–110 mg L–1) on dye removal were studied. Batch experiments were carried out for biosorption kinetics and isotherm studies. The results showed that dye uptake capacity was found to increase with a decrease in biosorbent dosage. Equilibrium uptake capacity was found to be greatest at a pH value of 2.0, when compared to all other pH values studied. The equilibrium biosorption isotherms were analyzed by the Freundlich and Langmuir models. The equilibrium data was found to fit very well with the Freundlich isotherm model when compared to the Langmuir isotherm model. The kinetic data was analyzed using pseudo-first order and pseudo-second order kinetic models. From the results, it was observed that the kinetic data was found to fit the pseudo-second order kinetic model very well. The surface morphology of the stem of the N. rubra biosorbent was exemplified by scanning electron microscopy. Fourier transform infrared analysis was employed to confirm the existence of an amine group in the stem of N. rubra.  相似文献   
55.
Halogen contents for the widely distributed reference glasses BHVO‐2G, BIR‐1G, BCR‐2G, GSD‐1G, GSE‐1G, NIST SRM 610 and NIST SRM 612 were investigated by pyrohydrolysis combined with ion chromatography, total reflection X‐ray fluorescence analysis, instrumental neutron activation analysis, the noble gas method, electron probe microanalysis and laser ablation‐inductively coupled plasma‐mass spectrometry. Glasses BHVO‐2G, GSD‐1G and GSE‐1G have halogen contents that can be reproduced at the 15% level by all bulk techniques and cover a significant range in halogen mass fractions for F (~ 20–300 μg g?1), Cl (~ 70–1220 μg g?1) and Br (~ 0.2–285 μg g?1) and I (~ 9–3560 ng g?1). The BIR‐1G glass has low F (< 15 μg g?1), Cl (~ 20 μg g?1), Br (15 ng g?1) and I (3 ng g?1). The halogen contents for the silica‐rich NIST SRM 610 and 612 glasses were poorly reproduced by the different techniques. The relatively high Cl, Br and I abundances in glasses GSD‐1G and GSE‐1G mean that these glasses are well suited for calibrating spatially resolved micro‐analytical studies on silicate glasses, melt and fluid inclusions. Combined EPMA and laser ablation‐inductively coupled plasma‐mass spectrometry data for glass GSE‐1G demonstrate homogeneity at the 10% level for Cl and Br.  相似文献   
56.
中国含盐盆地赋存丰富的盐湖卤水和深部卤水资源,卤水中富集溴(Br)元素,具有潜在的开发利用价值。Br作为盐湖卤水中重要的资源元素,目前对其分布规律和物质来源的系统对比研究鲜有报道。本文以柴达木盆地察尔汗盐湖四个区段晶间卤水为研究对象,分析整个湖区Br元素分布规律和物质来源,对比中国不同含盐盆地卤水Br资源变化和物源联系,并总结不同卤水开发利用价值。结果表明:① 察尔汗盐湖Br含量呈东高西低特征且不同区段差异明显;② 别勒滩和达布逊区段卤水低Br受河流补给并经蒸发富集,而察尔汗和霍布逊区段高Br受北部断裂带上涌富Ca泉水补给;③ 中国含盐盆地(柴达木盆地、库车盆地、江汉盆地、吉泰盆地)大部分深部卤水高Br值主要受水- 岩反应、沉积物及有机质中Br的解吸获得;④ 盐湖晶间卤水虽远不及深部卤水Br含量高,但其优点在于便于开发、综合利用率高,尤其浓缩卤水及老卤中的Br含量可预见性的高于工业开采品位,是当下和今后值得关注的资源。  相似文献   
57.
薄膜吸附制样-波长色散X射线荧光光谱法测定卤水中的溴   总被引:2,自引:2,他引:0  
溴主要以离子形式分布在地壳水圈的溴化物型卤水、卤化物硫酸盐型卤水中,目前应用波长色散X射线荧光光谱(WDXRF)测定卤水中的溴,主要采用粉末载体压片法前处理待检样品,制样工作量大,制样均匀性和制样过程中的污染都会影响准确度,方法实用性不强。本文借助薄膜吸附前处理卤水样品,通过优化筛选薄膜材料及卤水取样量,确定移取50μL卤水样品滴于Ф=40 mm的3#层析滤纸的圆心位置,自然晾干后高压压平来前处理待检样品,采用人工配制标准样品校正溴的标准曲线,用WDXRF测定溴的含量。钾钠钙镁氯和硫酸根等共存离子的影响可以忽略,方法检出限(3σ)为0.95 mg/L,精密度(RSD,n=11)不大于0.8%,加标回收率为99.4%~101.2%。本方法操作简便,不需要使用化学试剂,解决了现行卤水中溴的分析方法流程复杂、分析成本高的问题。  相似文献   
58.
建立了利用GasBenchⅡ联用同位素比值质谱仪(GasBench Ⅱ-IRMS)用于测定地下水中溴稳定同位素的方法。基于溴比氯更容易被重铬酸钾氧化的性质,将Br-氧化成Br2,而氯残留在原溶液中,从而把溴与氯分离开;再利用AgNO3将溴以AgBr的形式沉淀下来,然后将AgBr转化成CH。Br进行溴稳定同位素质谱测定。反应中,CHsI用量为20μL,AgBr用量为0.5mg。本测试流程需溴4~10mg,质谱测试时问由1.5h缩短为800s,测试精度优于±0.1‰(2σ)。该方法可以用于地下水中溴同位素测定,在水文地质研究中具有广阔的应用前景。  相似文献   
59.
Adsorption of reactive black 5 (RB5) from aqueous solution onto chitosan was investigated in a batch system. The effects of solution pH, initial dye concentration, and temperature were studied. Adsorption data obtained from different batch experiments were modeled using both pseudo first‐ and second‐order kinetic equations. The equilibrium adsorption data were fitted to the Freundlich, Tempkin, and Langmuir isotherms over a dye concentration range of 45–100 µmol/L. The best results were achieved with the pseudo second‐order kinetic and Langmuir isotherm equilibrium models, respectively. The equilibrium adsorption capacity (qe) was increased with increasing the initial dye concentration and solution temperature, and decreasing solution pH. The chitosan flakes for the adsorption of the dye was regenerated efficiently through the alkaline solution and was then reused for dye removal. The activation energy (Ea) of sorption kinetics was estimated to be 13.88 kJ/mol. Thermodynamic parameters such as changes in free energy (ΔG), enthalpy (ΔH), and entropy (ΔS) were evaluated by applying the van't Hoff equation. The thermodynamics of reactive dye adsorption by chitosan indicates its spontaneous and endothermic nature.  相似文献   
60.
Understanding absorbance photobleaching of marine dissolved organic matter (DOM) is important because DOM chromophores impact oceanic primary productivity by affecting the depth of the photic zone, absorb UV radiation and affect ocean color used in remote sensing. However, the fundamental mechanisms which account for this bleaching are largely unknown. Controlled laboratory studies demonstrated that the presence of seawater concentrations of chloride and bromide ions enhanced absorbance photobleaching reaction rates by ~ 40%, regardless of DOM source or the presence or absence of carbonate ions. In contrast, halide ions generally did not affect fluorescence bleaching rates. Variations in ionic strength did not alter the enhancement in absorbance photobleaching by halide ions. Accordingly, the enhancement in absorbance photobleaching was specific to halide ions, rather than a generalized salinity effect. We confirmed the formation of hydroxyl radical (HO) in illuminated samples, and its significant scavenging in the presence of halide salts. Gamma-radiolysis experiments and associated modeling indicated that a small component (~ 12%) of the photobleaching enhancement by halides was consistent with the hypothesis that halide scavenging of HO will form reactive halogen radicals that target electron-rich chromophores within DOM more selectively than HO. The mechanism responsible for the major component of absorbance photobleaching rate enhancement by halides remains unresolved.  相似文献   
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