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991.
该文制备了一种可在pH 5.0~9.0范围内选择性吸附As(Ⅲ)的巯基(—SH)修饰的环氧基改性磁性纳米材料(Fe3O4@SiO2@GMA—S—SH MNPs),将其与新型MSPE-ICP-MS联用实现了水中As(Ⅲ)和As(Ⅴ)的分离分析,As(Ⅴ)经Na2S2O3/KI还原后,采用MSPE-ICP-MS测得总砷含量,然后通过差减法计算。结果显示,方法对As(Ⅲ)的检出限(LOD)为1.5 ng·L-1,富集倍数为150倍,线性范围为5~3 000 ng·L-1,相对标准偏差(RSD)(c=10 ng·L-1,n=7)为9.6%。将该方法用于水质标准样品(GSB07-3171-2014)中无机砷形态分析,测定结果与参考值一致。采用该方法测定自来水As(Ⅲ)和As(Ⅴ)的含量分别为0.036、0.043 μg·L-1,湖水中含量分别为0.24、0.43 μg·L-1,加标回收率为80.9%~101%,RSD为1.5%~10%。该方法具有检出限低、富集倍数大、吸附/解吸动力学快、抗干扰能力强等优点,可用于实际水样中无机砷的形态分析。 相似文献
992.
993.
Dr. Marwa Abdelmouleh Dr. Mathieu Lalande Edith Nicol Dr. Gilles Frison Prof. Dr. Guillaume van der Rest Dr. Jean-Christophe Poully 《Chemphyschem》2021,22(12):1243-1250
These last decades, it has been widely assumed that 18-crown-6-ether (CE) plays a spectator role during the chemical processes occurring in isolated host-guest complexes between peptides or proteins and CE after activation in mass spectrometers. Our present experimental and theoretical results challenge this hypothesis by showing that CE can abstract a proton or a protonated molecule from protonated peptides after activation by collisions in argon or electron capture/transfer. Furthermore, thanks to comparison between experimental and calculated values of collision cross-sections, we demonstrate that CE can change binding site after electron transfer. We also propose detailed mechanisms for these processes. 相似文献
994.
Moment analysis method using partial filling CE was developed for the kinetic study on solute permeation at the interface of spherical molecular aggregates. Moment equations for partial filling CE were developed by classifying CE systems into five categories according to the migration velocities of solute and molecular aggregate. The method was applied to the study on the dissolution of electrically neutral solutes into SDS micelles. Elution peaks were measured by partial filling CE while changing the concentration of SDS and the filling ratio of SDS micellar zone to the capillary (ϕM). Partition equilibrium constants (Kp) and rate constants of interfacial solute permeation of SDS micelles (kin and kout) were determined from the first absolute and second central moments of the elution peaks by using the moment equations. Their values were comparable irrespective of ϕM and were almost the same as those previously measured by complete filling CE. The positive correlation of Kp with the hydrophobicity of the solutes was explained in terms of the change in kin and kout. It was demonstrated that the moment analysis method using partial filling CE is effective for studying solute permeation kinetics at the interface of spherical molecular aggregates. 相似文献
995.
Microplastics (MPs) have gained significant attention in the last two decades and have been widely researched in the marine environment. There are, however, less studies on their presence, routes of entry, and impacts on the biota in the soil environment. One of the main issues in the study of MPs is a lack of standardized methods for their identification in environmental samples. Currently the most commonly used techniques are thermal desorption gas chromatography–mass spectrometry (GC–MS) methods and pyrolysis followed by GC–MS. In this study, headspace-solid phase microextraction followed by GC–MS is proposed as a simple and widely applicable method for the determination of commonly present polymer MPs (polyethylene terephthalate, polystyrene, polyvinyl chloride, polyethylene, and polypropylene) in environmental samples, for analytical laboratories with basic equipment worldwide. The proposed method is based on the identification of compounds, which are formed during the well-controlled melting process of specific coarse (1–5 mm) and fine fraction (1 mm–100 μm) MPs. The method was upgraded for the identification of individual polymer type in blends and in complex environmental matrices (soil and algae biomass). The successful application of the method in complex matrices makes it especially suitable for widescale use. 相似文献
996.
该研究利用超高效液相色谱-串联四极杆静电场轨道阱高分辨质谱(UHPLC/ESI-Q-Orbitrap)技术,对硒代蛋氨酸(SeMet)的色谱信息、分子离子质荷比和碎裂片段的质荷比进行采集,并对特征离子碎裂途径进行解析,建立了豆类中硒代蛋氨酸的检测方法。样品用三羟甲基氨基甲烷-盐酸(Tris-HCl)缓冲溶液溶解后,涡旋混匀,超声提取,在恒温水浴条件下酶解,离心后取上清液过0.22μm滤膜后上机检测。采用Hypersil GOLD HILIC(50 mm×2.1 mm,1.9μm)色谱柱进行分离,以0.2%(体积分数,下同)甲酸6 mmol/L甲酸铵水溶液和0.2%甲酸6 mmol/L甲酸铵乙腈溶液为流动相梯度洗脱,采用电喷雾正离子模式电离,在全扫描/数据依赖扫描模式(Full MS/dd-MS2)下进行检测,基质匹配标准校正法定量。结果表明,硒代蛋氨酸的基质效应为15.75%,在0.05~0.5 mg/L范围内线性关系良好,相关系数(r2)为0.9976,方法检出限(LOD)为0.015 mg/kg,定量下限(LOQ)为0.05 mg/kg;空白样品在0.1、0.2、0.4 mg/kg 3个加标水平下的平均回收率为77.6%~83.2%,日内相对标准偏差(RSDr)为2.8%~4.8%,日间相对标准偏差(RSDR)为4.1%~6.5%。将方法应用于实际样品的检测,得富硒黑豆、富硒红豆、富硒绿豆中硒代蛋氨酸的含量分别为0.252、0.163、0.184 mg/kg。该方法具有前处理操作简单、结果准确、重复性好等优点,适用于豆类中硒代蛋氨酸的检测。 相似文献
997.
任梦阳 《中国无机分析化学》2022,12(2):52-55
建立了氟化氢铵消解地球化学样品,电感耦合等离子体质谱(IC P-M S)法测定样品中钨、锡和钼的方法.方法经过国家土壤和水系沉积物标准参考物质验证,方法的检出限钨为0.048μg/g、锡为0.079μg/g、钼为0.063μg/g,准确度(相对误差)钨为0.64% ~6.28%、锡为0.29% ~3.74%、钼为2.1... 相似文献
998.
超高效液相色谱-四极杆/静电场轨道阱高分辨质谱法非靶向筛查苹果中苯脲类农药 总被引:1,自引:0,他引:1
建立了超高效液相色谱-四极杆/静电场轨道阱高分辨质谱(UPLC-Q/Orbitrap HRMS)非靶向筛查苹果中苯脲类农药的方法。样品采用QuEChERS法提取净化,Acquity BEH C18色谱柱(100 mm × 2.1 mm,1.7 μm)分离,以甲醇和含0.1%甲酸的水溶液为流动相进行梯度洗脱,在电喷雾正离子模式下采用四极杆/静电场轨道阱高分辨质谱进行检测。将13种苯脲类除草剂和9种苯甲酰脲类杀虫剂按化学结构分为4类。首先通过对4类22种典型苯脲类农药标准品的准分子离子和二级质谱碎片进行分析,总结苯脲类农药的质谱裂解规律如下:绿麦隆等9种苯脲类除草剂的主要特征离子碎片为m/z 72.044 59,可通过特征丢失中性分子二甲胺(m/z 45.058 03)产生特征离子碎片;绿谷隆等4种苯脲类除草剂可通过特征丢失中性分子甲醇[CH3OH]或卤化氢[HR1](R=Cl,Br,F)产生离子碎片;除虫脲等7种含氟苯甲酰脲杀虫剂的主要特征离子碎片为 m/z 158.040 47、141.015 00,也可发生特征中性丢失2,6-氟苯甲酰胺结构[C8H3F2O2NH2](m/z 183.013 21);杀铃脲等2种含氯苯甲酰脲类杀虫剂的主要特征离子碎片为m/z 156.020 25、138.993 76、113.015 28。利用该方法对北京12份市售苹果进行非靶向筛查,在1份样品中筛查出绿麦隆。该方法可为快速筛查农产品中相似结构特征的苯脲类化合物提供参考。 相似文献
999.
The molecular species of phosphatidylcholine from freshwater sources (Macrobranchium nipponense and Macrobranchium rosenbergii) and marine sources (Euphausia superba and Penaeus chinesis) were characterized by high-resolution mass spectrometry. The tandem secondary mass spectrometry (MS/MS) fragmentation allowed for the identification of fatty acyl residues of phosphatidylcholine molecular species. (16:0–18:1)Phosphatidylcholine was the main phosphatidylcholine molecular species determined in all shrimp samples, especially in E. superba. Macrobranchium rosenbergii phosphatidylcholine was particularly rich in (16:0–20:5)phosphatidylcholine and (16:0–22:6)phosphatidylcholine. The proportion of the two molecular species was next to the phosphatidylcholine of E. superba. Therefore, M. rosenbergii appears to be a potential freshwater source for the supplementation of polyunsaturated fatty acids, particularly eicosapentaenoic acid (20:5) and docosahexaenoic acid (22:6). This approach may be used as an efficient method for the identification of natural phosphatidylcholine sources from the broad range of plant, animal, and marine origins. 相似文献
1000.
仪器设备的期间核查是实验室管理及实验室认证认可的一项基本要求,辉光放电质谱仪主要应用于高纯金属材料的分析,标样研制较为困难,使用高纯标准物质进行质量控制及期间核查的方法难以实现。对用液氮低温冷却离子源型的辉光放电质谱仪,使用纯钽片在进行日常仪器调试信号时得到的钨元素含量数据,用于绘制平均值-极差控制图作为实验室质量控制及期间核查的判定依据,以此评价仪器日常工作的性能状态,以保证检测结果的正确性和可靠性。 相似文献