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本文采用氢化物-非色散原子荧光光谱法研究了十几种饲料矿物添加剂中金属离子对砷测定的干扰,采用加入硫脲-抗坏血酸混合溶液、碘化钾分离、加热蒸干等方法消除干扰。同时本文还对测定砷的酸度、硼氢化钾浓度和仪器工作参数进行了研究和优化。方法相对标准偏差(RSD)为0.54%,检出限(D.L)为54.5ng/L,样品国.加标回收率为102.9%。实际样品测定结果与胂斑法相比具有很好的一致性。 相似文献
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本文对镍氢动力电池用AB5型纳米晶贮氢合金热处理工艺进行了研究.分别采用X射线衍射、金相、PCI测试手段分析热处理后贮氢合金的微观结构与吸放氢动力学性能.贮氢合金的电性能测试结果表明,经过950℃×6 h热处理的贮氢合金,10C放电比容量可以达到241mAh/g,循环寿命大于500次,分别以7C,10C放电,高倍率放电率(HRD)为92.5%,85.2%.将贮氢合金粉组装成电池进行测试,2min后,放电平台电压为1.143V,以10C放电,300次循环后,电池容量衰减率较小. 相似文献
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膜渗透与离子色谱联用技术测定蔬菜中亚硝酸盐和硝酸盐 总被引:1,自引:0,他引:1
建立了膜渗析与离子色谱联用技术分析蔬菜等复杂基体中亚硝酸盐和硝酸盐的方法。蔬菜样品经沸水浴后,试样液通过膜渗析除去水溶性大分子杂质和颗粒,直接进入离子色谱分析。渗析池采用0.20μm的醋酸纤维为渗析膜,以水为接收液,分析柱为Metrosep A Supp4-250阴离子交换柱,以1.8mmol/L Na2CO3 1.7mmol/L NaHCO3为流动相,采用化学抑制电导检测。以20g称样计量,方法中NO2-、NO3-的检出限分别为0.075mg/kg和0.105mg/kg;实际样品的加标回收率分别为80.6%~98.7%和90.5%~114%;相对标准偏差(RSD)≤10%。本方法前处理简单,重现性好,准确度高。 相似文献
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This paper presents a mathematical model to describe a two-fluid electroosmotic pumping technique, in which an electrically non-conducting fluid is delivered by the interfacial viscous force of a conducting fluid; the latter is driven by electroosmosis. The electrical potential in the conducting fluid and the analytical solution of the steady two-fluid electroosmotic stratified flow in a rectangular microchannel was presented by assuming a planar interface between the two immiscible fluids. The effects of viscosity ratio, hold-up, concentration, and interfacial zeta potential are analyzed to show the potential feasibility of this technique. 相似文献
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Yulu Yang Mingguang Wu Xingwang Zhu Hui Xu Si Ma Yongfeng Zhi Hong Xia Xiaoming Liu Jun Pan Jie-Yinn Tang Siang-Piao Chai Leonardo Palmisano Francesco Parrino Junli Liu Jianzhong Ma Ze-Lin Wang Ling Tan Yu-Fei Zhao Yu-Fei Song Pardeep Singh Pankaj Raizada Deli Jiang Di Li R. A. Geioushy Jizhen Ma Jintao Zhang Song Hu Rongjuan Feng Gang Liu Minghua Liu Zhenhua Li Mingfei Shao Neng Li Jiahe Peng Wee-Jun Ong Nikolay Kornienko Zhenyu Xing Xiujun Fan Jianmin Ma 《中国化学快报》1990,30(12):2065-2088
This roadmap demonstrates a series of two-dimensional nanomaterials, such as graphene, black phosphorus, oxides, layered double hydroxides, chalcogenides, bismuth-based layered compounds, MXenes, metal organic frameworks, covalent organic frameworks, and others, for environmental catalysis. 相似文献
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Ping Wang Yi-Zeng Liang Ben-Mei Chen Neng Zhou Lun-Zhao Yi Yan Yu Zhi-Biao Yi 《Chromatographia》2007,65(3-4):209-215
A rapid, simple and specific liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) method has been developed
and validated for the simultaneous determination of enalapril and its major active metabolite enalaprilat in human plasma.
Benazepril hydrochloride was used as the internal standard. Plasma was deproteinized with acetone and centrifuged. The supernatant
was transferred and evaporated to dryness and the residue dissolved in mobile phase. Samples were separated on a C18 column
with a mobile phase of methanol–20 mM ammonium acetate (53:47, v/v) containing 0.15% trifluoracetic acid (v/v) with a pH of 3.0. Enalapril, enalaprilat and the internal standard were measured by electrospray positive selective ion
monitoring mode. The method was validated over a linear range of 1.56–400 ng mL−1 and the limits of quantification were 1.56 ng mL−1 for both enalapril and enalaprilat using 0.1 mL plasma. Extraction efficiency was more than 84% and recoveries were in range
of 93.65–101.17%. The intra-day relative standard deviations (RSD) were less than 8.16 and 7.05% and inter-day RSDs were within
8.42 and 5.72% for enalapril and enalaprilat, respectively. The storage stability of QC samples was investigated under various
conditions. The method was successfully applied for the evaluation of the pharmacokinetics and bioequivalence of enalapril
and enalaprilat in 20 healthy volunteers after an oral dose of 20 mg enalapril maleate. 相似文献
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通过4,4’-一氧二(异氰酸苯酯)与异丙醇加成反应,合成标题化合物 4,4’-一氧二(苯胺灵)(Ⅰ) (C20H24N2O5, Mr=372.41),并用X射线衍射、红外光谱、13C核磁共振、电子轰击质谱和元素分析对标题化合物进行表征. 晶体属于三斜晶系,空间群为P1晶体学参数为: a=0.85107(17), b=0.91164(18), c=1.45701(3) nm, α=80.44(3)°, β=85.25(3)°, γ=62.88(3)°, V=0.9922(3) nm3, Z=2, Dc=1.247 g•cm-3, μ(Mo Kα)=0.90 cm-1, F(000)=396.两个苯环平面之间的夹角为62.06° (0.06°). 晶体结构经全矩阵最小二乘法修正,最终偏离因子R=0.0520, wR=0.1434(对可观察点).此化合物应具有广谱的生物活性. 相似文献