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71.
72.
A Urey-Bradley force field, determined from vibrational frequencies of furan and six of its deuterated derivatives, has been used to compute the normal vibrations of α substituted compounds which possess a furan ring. Theoretical results give good interpretations of the vibrational spectra. 相似文献
73.
为研究摩天岭花岗岩体的地质及地球化学特征,分别测定了该岩体的主量元素,微量元素和稀土元素含量,并作了图解分析。结果表明,摩天岭花岗岩体在主量元素特征上表现为富钾,低钠、较低的/7,(Na2O)/n(K2O),贫钙镁,富铁,w(A)/w(CNK)〉1.1,为强过铝质,具有华南产铀花岗岩的基本特征。微量元素特征表现为:富集强不相容元素,尤其是Rb、Th元素;而贫弱不相容元素zr、Hf、Sm、Y和Yb。Sr元素呈强烈亏损。稀土总含量较低,具有较低的轻重稀土分异,略富集LREE,亏损HREE,具有较低的埘(La)/w(Yb)。岩体具有强烈的负8Eu异常。摩天岭花岗岩体的岩石类型及地球化学特征表明其是S型花岗岩,其形成的构造环境判别图解显示摩天岭岩体具有火山弧花岗岩和同碰撞花岗岩的双重属性。 相似文献
74.
对北黄海中部DLC70-2孔166个沉积物样品进行了稀土元素测定,结合粒度参数研究,以探讨北黄海中部DLC70-2孔稀土元素地球化学特征和物质来源。结果表明:DLC70-2孔岩心稀土元素分布特征分别反映了末次间冰期(暖期)晚期以来北黄海海面波动以及沉积物物源的变化。判别函数和稀土元素配分模式表明北黄海DLC70-2孔沉积物物源主要为黄河源和鸭绿江源。La/Yb判别图解揭示DLC70-2孔上部0~32.10 m和下部37.60~60.72 m沉积物以黄河源为主,中部32.10~37.60 m和底部60.72~70.45 m沉积物以鸭绿江源为主。研究表明晚更新世以来黄河对北黄海中部沉积起着重要作用,而鸭绿江物质对北黄海中部沉积作用也有明显影响。 相似文献
75.
WANG Ying WANG Kun BAO Yong-li WU Yin MENG Xiang-ying LI Yu-xin 《高等学校化学研究》2007,23(3):310-313
The root of Panax ginseng plant undergoes a specific developmental process to become a biosynthesis and accumulation tissue for ginsenosides. To identify and analyze genes involved in the biosynthesis of ginsenoside, we constructed and characterized a full-length cDNA library for 6-year-old North American ginseng. The titer of primary cDNA library is 1.2 × 10^6 pfu/mL, the titer of amplified library is 2. 6 × 10^10 pfu/mL and the rate of recombinant is above 86%. The insert size ranges from 0. 3 to 2.0 kb. Sequencing results show that 18 of 58 genes are high homologous to the genes (GBRS, GBR3 and GBR1 ) known in GenBank, which are involved in biosynthesis of ginsenoside in North American ginseng plant; 16 of 58 genes are novel genes. The full-length cDNA library of North American ginseng root tissues is essential for the cloning of genes known and it is also an initial key for the screening and cloning of new genes. 相似文献
76.
K. Wille J. Vanden Bussche H. Noppe E. De Wulf P. Van Caeter C.R. Janssen H.F. De Brabander L. Vanhaecke 《Journal of chromatography. A》2010,1217(43):6616-6622
Perfluorinated compounds (PFCs), which are extensively used in a wide variety of applications because of their specific surfactant properties, have recently appeared as an important new class of global environmental pollutants. Quantitative analysis of PFCs in aqueous matrices remains, however, a challenging task. During this study, a new analytical method for the determination of 14 PFCs in surface-, sewage- and seawater was developed and validated. The target analytes were extracted using solid-phase extraction followed by liquid chromatography coupled to a time-of-flight mass spectrometer (LC–ToF-MS). The use of very narrow mass tolerance windows (<10 ppm) resulted in a highly selective MS-technique for the detection of PFCs in complex aqueous matrices. Validation of this analytical method in surface-, sewage- and seawater resulted in limits of quantification (LOQs) varying from 2 to 200 ng L−1, satisfying recoveries (92–134%), and good linearity (R2 = 0.99 for most analytes). Analysis of samples of the North Sea, the Scheldt estuary, and three harbours of the Belgian coastal region led to the detection of four different PFCs. Perfluorooctane sulfonate (PFOS) was found to be the most abundant PFC in levels up to 38.9 ng L−1. 相似文献
77.
Variability of SO2 in an intensive fog in North China Plain:Evidence of high solubility of SO2 总被引:1,自引:0,他引:1
Qiang Zhang Xuexi Tie Weili Lin Junji Cao Jiannong Quan Liang Ran Wanyun Xu 《中国颗粒学报》2013,11(1):41-47
A field experiment was conducted in an intensive fog event between November 5 and November 8,2009, in a heavily SO2-polluted area in North China Plain(NCP),to measure SO2 and other air pollutants,liquid water content(LWC) of fog droplets,and other basic meteorological parameters.During the fog period, the concentrations of SO2 showed large variability,which was closely related to the LWC in the fog droplets.The averaged concentration of SO2 during non-fog periods was about 25 ppbv,while during the fog period,it rapidly reduced to about 4-7 ppbv.Such large reduction of SO2 suggested that a majority of SO2(about 70%-80%) had reverted from gas to aqueous phase on account of the high solubility of SO2 in water in the fog droplets.However,the calculated gas to aqueous phase conversion was largely underestimated by merely using the Henry’s Law constant of SO2,thus suggesting that aqueous reaction of SO2 in fog droplets might play some important role in enhancing the solubility of SO2.To simplify the phenomenon,an effective solubility coefficient is proposed in this study.This variability of SO2 measurement during the extensive fog event provides direct evidence of oxidation of SO2 in fog droplets, thus providing important implications for better understanding of the acidity in clouds,precipitation,and fogs in NCP,now a central environmental focus in China due to its rapid economic development. 相似文献
78.
Chloroacetyl chloride is studied by gas-phase electron diffraction at nozzle-tip tempera- tures of 18, 110 and 215°C. The molecules exist as a mixture of anti and gauche confor- mers with the anti form the more stable. The composition (mole fraction) of the vapor with uncertainties estimated at 2σ is found to be 0.770 (0.070), 0.673 (0.086) and 0.572 (0.086) at 18, 110 and 215°C, respectively. These values correspond to an energy difference with estimated standard deviation ΔEo = Eog -Eoa = 1.3 ± 0.4 kcal mol?1 and an entropy difference ΔSo = Sog -Soa = 0.7 ± 1.1 cal mol?1 K?1. Certain of the diffraction results permit the evaluation of an approximate torsional potential function of the form 2V = V1(1 - cos φ) + V2(1 - cos 2φ) + V3(1 - cos 3φ); the results are V1 = 1.19 ± 0.33, V2 = 0.56 ± 0.20 and V3 = 0.94 ± 0.12, all in kcal mol?1. The results for the distance (ra), angle (∠α) and r.m.s. amplitude parameters obtained at the three temperatures are entirely consistent. At 18°C the more important parameters are, with estimated uncertainties of 2σ, r(C-H) = 1.062(0.030) Å, r(CO) = 1.182(0.004) Å, r(C-C) = 1.521(0.009) Å. r(CO-Cl) = 1.772(0.016) Å, r(CH2-Cl) = 1.782(0.018) Å, ∠C-C-0 = 126.9(0.9)°, ∠CH2-CO-C1 = 110.0(0.7)°,∠CO-CH2-C1 = 112.9(1–7)°, ∠H-C-H = 109.5° (assumed), ∠φ (gauche torsion angle relative to 0° for the anti form) = 116.4(7.7)°, δ (r.m.s. amplitude of torsional vibration in the anti conformer) == 17.5(4.2)°. 相似文献
79.
80.
广西车田红辉沸石对不同离子吸附性的初步研究 总被引:6,自引:0,他引:6
研究表明,不同粒度的红辉沸石在不同的温度条件下对K^ 、Na^ 、Ca^2 、Mg^2 、NH4^ 等离子具有不同的吸附容量。在30℃时,8μm的红辉沸石对K^ 、Na^ 、Ca^2 、Mg^2 、NH4^ 的吸附量分别为:10.90mg/g、10.01mg/g、7.64mg/g、5.50mg/g、108.70mmol/100g;45μm的红辉沸石对K^ 、Na^ 、Ca^2 、Mg^2 、NH4^ 的吸附量分别为:10.10mg/g、9.80mg/g、6.90mg/g、5.08mg/g、101.10mmol/100g;246μm的红辉沸石对K^ 、Na^ 、Ca^2 、Mg^2 、NH4^ 的吸附量分别为:2.66mg/g、2.20mg/g、1.86mg/g、1.26mg/g、28.00mmol/100g;在2℃时,8μm的红辉沸石对K^ 、Na^ 、Ca^2 、Mg^2 、NH4^ 的吸附量分别为:10.60mg/g、9.82mg/g、6.90mg/g、5.07mg/g、99.60mmol/100g。在常温25-30℃,湿度82%条件下,246μm、45μm、8μm的红辉沸石含水率为7.06%、7.25%、7.78%。 相似文献