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41.
G. Wu R. M. Izatt M. L. Bruening W. Jiang H. Azab K. E. Krakowiak J. S. Bradshaw 《Journal of inclusion phenomena and macrocyclic chemistry》1992,13(2):121-127
The aqueous protonation and anion-binding SeO
2
–/4
SO
2–
4
, and NO
–
3
) constants of the macrocyclic polyamine ligand, dipyridino-hexaaza-28-crown-8(L), were measured in 0.1M KCl using a potentiometric titration technique. The protonation sequence of the aza groups of L was studied in D2O from the chemical shifts of the nonlabile protons so as to find the charge distribution geometry as a function of pD. The study indicates that in 0.1M KC1 fully protonated L forms stable l: 1 complexes with SeO
2–
4
(logK=3.68) and SO
2–
4
(logK=3.55), but not with NO
–
3
(logK < l.5). All of the amine pK values were above 6.3, thus allowing the use of the protonated form of this ligand over a wide pH range. 相似文献
42.
无机材料的微观结构决定了材料的许多特性,如传输行为、催化活性、分离效率、粘附、储存和释放动力学。具有管状结构纳米尺度的材料由于其特殊的结构及由此带来的特殊性能正成为一个令人兴奋的化学研究领域。文章综述了近年来无机纳米管材料的合成途径和进展。 相似文献
43.
Ramasamy、Osuka等用NaHTe/EtOH研究了二卤代物的脱邻二溴、偕二溴反应和α-溴代羰基化合物的脱卤还原反应,我们选择结构不同的卤代物以NaHTe还原,发现在水介质和催化量碲代替计算量碲时也能顺利地进行这类反应,其反应条件温和,产率高,是有机官能团转化的好方法。 相似文献
44.
以Ce ZrO2为基体,通过复合不同加入量的第二相CePO4颗粒,研究了陶瓷材料力学性能的变化,并借助加载能谱仪(EDS)的扫描电子显微镜(SEM)对材料弯曲断口及压痕裂纹扩展方式进行分析。当CePO4加入量为25%时,虽然材料力学性能有一定下降,但已经能用WC刀具进行加工。材料的弯曲断口显示,CePO4在两相体系中的断裂呈层片状形式;加入CePO4后,由于两相之间弱结合界面的存在,压痕裂纹扩展形式发生明显变化,由连续扩展机制过渡为不连续扩展。由这两种机制形成的材料断裂过程是阶段性的,在实际中可以用作材料最终破坏前的预报。 相似文献
45.
Y2O3, La2O3, Sm2O3对氧化铝瓷烧结及力学性能的影响 总被引:16,自引:3,他引:16
研究了3种稀土氧化物对氧化铝陶瓷烧结性能和力学性能的影响.结果表明 含Y2O3,La2O3,Sm2O3的添加剂促进了氧化铝瓷的烧结,提高了氧化铝瓷的力学性能.Y2O3和Sm2O3掺量为0.50%,La2O3掺量为0.75%时氧化铝瓷在1600或1620 ℃保温2 h烧结,相对密度达98.9%以上,强度超过439 MPa,断裂韧性达5.15 MPa·m1/2以上.微观结构分析表明,Y2O3,La2O3,Sm2O3抑止氧化铝晶粒生长,细化晶粒,使晶粒尺寸较均匀形成致密化结构. 相似文献
46.
A composite film of ethylenediamine tetraacetic acid (EDTA)‐ZrO2 organic‐inorganic hybrid was prepared based on the chelation between Zr(IV) and EDTA. The direct electrochemical behavior of cytochrome c (cyt. c) at the hybrid film modified glassy carbon electrodes was investigated. The immobilized EDTA can promote the redox of heme in horse heart cyt. c which gives rise to a pair of reversible redox peaks with a formal potential of 40 mV (vs. SCE). The peak current increased linearly with the increase of cyt. c concentration in the range of 1.6 × 10?6—8.0 × 10?5 mol·L?1 with the correlation coefficient of 0.996. Further investigation shows that metal ions can impede the electron transfer of cyt. c. The impediment capability of metal ions depends on their coordination capability with EDTA and their valence number. 相似文献
47.
Sm2O3掺杂CeO2纳米粉体的烧结动力学 总被引:2,自引:0,他引:2
对Sm2O3掺杂CeO2纳米粉体的烧结性能进行了研究, 得出等速烧结过程中试样的线收缩率、密度、气孔率随烧结温度的变化规律, 它们随烧结温度的变化均呈"S"型曲线关系, 利用非线性回归了等速烧结过程动力学方程. 结果表明, Sm2O3掺杂CeO2纳米粉体的烧结过程分为3个阶段, 当烧结温度低于1000 ℃时, 线收缩率与密度变化较小, 处于烧结的初期; 在1000~1400 ℃时, 随着烧结温度的升高, 线收缩率与体积密度急剧增大, 材料开始烧结并致密化; 当烧结温度高于1400 ℃时, 线收缩率与体积密度趋于一恒定值, 材料已经致密化. 由归一化速率方程可知, 在T=1225 ℃时, 材料的烧结致密化速率最大. 相似文献
48.
Sodium phosphate tellurite glasses in the system (NaPO(3))(x)(TeO(2))(1-) (x) were prepared and structurally characterized by thermal analysis, vibrational spectroscopy, X-ray photoelectron spectroscopy (XPS) and a variety of complementary solid-state nuclear magnetic resonance (NMR) techniques. Unlike the situation in other mixed-network-former glasses, the interaction between the two network formers tellurium oxide and phosphorus oxide produces no new structural units, and no sharing of the network modifier Na(2)O takes place. The glass structure can be regarded as a network of interlinked metaphosphate-type P(2) tetrahedral and TeO(4/2) antiprismatic units. The combined interpretation of the O 1s XPS data and the (31)P solid-state NMR spectra presents clear quantitative evidence for a nonstatistical connectivity distribution. Rather, the formation of homoatomic P--O--P and Te--O--Te linkages is favored over mixed P--O--Te connectivities. As a consequence of this chemical segregation effect, the spatial sodium distribution is not random, as also indicated by a detailed analysis of (31)P/(23)Na rotational echo double-resonance (REDOR) experiments. 相似文献
49.
混合溶剂火焰原子吸收法直接测定原油中的镍刘广东袁存光张丙华刘文钦(石油大学(华东),山东东营257062)彭力(中国石油天然气总公司环保处,北京100724)关键词原油,混合溶剂,无机盐标准,原子吸收法,镍测定原油中,微量元素镍、钒、铁、铜的存在对... 相似文献
50.
A rapid, robust, sensitive and selective time-based flow injection (FI) on-line solvent extraction system interfaced with electrothermal atomic absorption spectrometry (ETAAS) is described for analyzing ultra-trace amounts of Cr(VI). The sample is initially mixed on-line with isobutyl methyl ketone (IBMK). The Cr(VI) is complexed by reaction with ammonium pyrrolidine dithiocarbamate (APDC), and the non-charged Cr(VI)–PDC chelate formed is extracted into IBMK in a knotted reactor made from PTFE tubing. The organic extractant is separated from the aqueous phase by a gravity phase separator with a small conical cavity and delivered into a collector tube, from which 55 μl organic concentrate is subsequently introduced via an air flow into the graphite tube of the ETAAS instrument. The operations of the FI-system and the ETAAS detector are synchronously coupled. A significant advantage of the approach is that matrix constituents, such as high salt contents, effectively are eliminated. The extraction procedure was optimized by a simplex approach. A central composite design was subsequently employed to verify the estimated operational optimum. An 18-fold enhancement in sensitivity of Cr(VI) was achieved after preconcentration for 99 s at a sample flow rate of 5.5 ml min−1, as compared to direct introduction of 55 μl of sample, yielding a detection limit (3σ) of 3.3 ng l−1. The sampling frequency was 24.2 samples h−1. The proposed method was successfully evaluated by analyzing a NIST Cr(VI)-reference material, synthetic seawater and waste waters, and waste water samples from an incineration plant and a desulphurization plant, respectively. 相似文献