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811.
We have analyzed the modifications of interaction energy between a molecule of hydrogen and graphene layers partially substituted
by boron. We show that the presence of boron modifies the symmetry of the energy landscape. It is due to both the larger boron
size (with respect to carbon) and its stronger interaction with hydrogen molecules. The changes of energy surface are not
confined to the neighborhood of substituted sites but extend over several graphene carbon sites, making the surface more heterogeneous.
We show that the average increase of adsorption energy could meet DOE targets for hydrogen storage if a partial charge transfer
between boron and hydrogen occurs during adsorption. 相似文献
812.
813.
The oil industry has been facing the challenges of separation of xylene isomers, o-xylene, m-xylene and p-xylene or removing them from the environment. In our present work, we investigated the adsorption of the three isomers on
two mesoporous materials, FDU-15-350 polymer and FDU-15-900 carbon materials. The isomer adsorption capacities are well correlated
with their physical pore properties. It is found that the micropores are very crucial for the adsorption of these three isomers.
The more micropore volume the adsorbent has, the better the adsorption capacity is. Henry’s constants were also calculated
for the three isomers on the two adsorbents. Both on FDU-15-350 polymer and FDU-15-900, the Henry’s constants for the three
isomers show the same trend o>m>p xylene which is coincidently in accordance with their polarity trend, indicating more polar adsorbate is preferred for adsorption
on the two adsorbents. The isosteric heats of adsorption are correlated with the microporosity and the size of the adsorbate
molecule. More microporosity and smaller molecules give higher heats of adsorption. Extracted information on pore properties
of adsorbents by using the three isomers has very similar results as that resolved from nitrogen adsorption, indicating the
feasibility of using the three isomers as adsorbates to extract pore information.
This work is devoted to commemorating the 60th birthday of Professor Mieczyslaw (Mietek) Jaroniec. 相似文献
814.
E. Giménez-Martín M. López-Andrade A. Ontiveros-Ortega M. Espinosa-Jiménez 《Cellulose (London, England)》2009,16(3):467-479
Comparative investigations of adsorption properties of chlorhexidine (CHX) on two cellulose fibers, bleached cotton and viscose,
were studied in order to obtain dry gauzes covered with known amount of this antiseptic. Adsorption isotherm results carried
out at 293 and 323 K can be described by Langmuir isotherm model, nevertheless, at high concentration correlation is better
to Freundlich isotherm. Electrokinetic potential evolution with CHX concentration, shows that initial negative zeta potential
of cotton and viscose diminish its absolute value as the concentration of the treatment increases; both fibers present an
isoelectric point at high concentration of CHX that is 0.3 mM for viscose and 0.8 mM for cotton. Electrostatic interactions
between cationic groups of CHX and carboxylic acid groups of the fibers could explain adsorption at low concentration, but
when it is higher than these values, possible hydrogen bonding between the amine groups of CHX and hydroxyl groups of cellulose
could explain increasing adsorption when it is hindered by electrostatic repulsion as it is predicted by Freundlich model,
that describes heterogeneous surface and multilayer adsorption. Adsorption kinetics isotherms reveal that the process is quick
with t
1/2 values of 5.4 min for cotton and 2.8 min for viscose. Differences in adsorption behaviour between the two fibers could be
attributed to structural differences as we have observed from estimation of CI index based on FTIR spectra. Values obtained
1.6 for viscose and 2.2 for cotton could explain that the amount of CHX adsorbed on viscose is higher than it is on cotton.
Finally desorption experiments performed with 0.01 M of NaCl solution at room temperature and pH 6 reveals the possibility
of therapeutical application of these fibers although further investigations must be done to optimize the process. 相似文献
815.
工业二乙烯苯悬浮聚合制备的大孔树脂,在二氯乙烷溶剂中以无水三氯化铁为催化剂进行悬挂双键后交联反应,得到的后交联树脂的比表面积和孔容都有显著增加.低温氮气吸附/脱附等温线得到的孔径分布曲线证明初始共聚物PDT-55(polydivinylbenzene,toluene as porogen)和PDH-55(polydivinylbenzene,heptane andtoluene as porogen)经后交联反应,所形成的新孔以微孔为主.树脂对水溶液中苯酚和维生素B12(VB12)的静态吸附研究发现树脂经后交联后,对苯酚的吸附量有显著提高,但对VB12的吸附量增加不大,原因是分子尺寸较大的VB12无法进入由悬挂双键后交联反应所形成的微孔.树脂PDT-55pc对苯酚的吸附量大于商品树脂XAD-4;后交联前后树脂PDT-55、PDT-55pc(post-crosslinking of PDT-55)、PDH-55、PDH-55pc(post-crosslinking ofPDH-55)对VB12的吸附量均大于树脂XAD-4.在本研究的实验条件下,Langmiur和Freundlich吸附等温线方程能很好地拟合树脂对水溶液中苯酚和VB12的吸附,相关系数在0.99以上.静态吸附动力学实验结果表明后交联前后树脂对苯酚的吸附较VB12更容易达到吸附平衡.吸附动力学数据的拟合结果显示,McKay二级吸附动力学模型符合树脂对苯酚的吸附,而对VB12的吸附更符合Lagergren一级吸附动力学模型. 相似文献
816.
合成了3种不对称结构的季铵盐Gemini表面活性剂a4-6-m, 分子的一根疏水链是偶氮苯为端基的4个亚甲基链, 另一根是不同长度的脂肪链(m=12, 14, 16). 研究结果表明, 反式偶氮苯封端的a4-6-m在气/液界面上以直立方式排列, 偶氮苯端基间的π-π相互作用导致吸附分子较为紧密地排列, 但吸附层外表面含有偶氮苯成分使临界胶束浓度(cmc)时的表面张力(γcmc)较大. 紫外光激发使反式结构偶氮苯变为顺式结构, 这些极性较强的顺式偶氮苯夹杂在直立的烷烃链间, 增强的偶极-偶极相互作用促进了分子紧密排列, 使分子占据面积(Amin)略微减小. 增长脂肪链长度有助于降低临界胶团浓度和C20(使水的表面张力降低20 mN·m-1时所需的表面活性剂浓度), 但对γcmc影响不大. 相似文献
817.
N是金刚石中的主要杂质之一, 为了研究金刚石生长过程中杂质N对C电子结构转化的影响, 用密度泛函理论研究了Ni(111)表面上C与N共吸附的三个不等价模型, 同时建立了三个C吸附模型作为比较. 计算结果表明, N原子的出现使得吸附体系相对不稳定, 吸附原子之间的相互作用不能忽略; 通过比较相互作用能可以看出, 相同的吸附位下C-C相互作用比C-N 相互作用强. 通过比较不同模型中C原子分波态密度可以看出, N-C相互作用一定程度上增加了Ni的催化活性, 但是与C-C自身的相互作用比较起来效果并不明显. 吸附几何结构和分波态密度还表明, 当吸附的原子过于紧密以致占有同一个Ni(111)-(1×1)晶胞表面时, 就会形成CN化合物或者类石墨杂质. 相似文献
818.
吸附树脂和活性炭对气体中苯的吸附研究 总被引:2,自引:0,他引:2
采用了动态吸附实验方法研究了吸附树脂NDA-201和椰壳型活性炭C1对苯蒸汽的吸附行为.对吸附平衡数据采用Dubinill-Astakov方程进行了拟合分析,并根据吸附剂孔结构特征探讨了吸附机理.实验结果表明,两种吸附剂的苯吸附等温线存在交叉现象,对高浓度苯蒸汽吸附治理可采用NDA-201树脂,低浓度则采用椰壳型活性炭C1;Dubinin-Astakov方程能用来对两种吸附剂的等温线进行拟合,表明吸附剂的微孔区域对吸附起着重要作用.微孔体积计算值的比较和特征曲线叠合的程度说明了.Polanyi吸附势理论更适合于描述椰壳型活性炭C1对苯的吸附,这可能是由于椰壳型活性炭C1的孔分布集中于微孔区,而NDA-201树脂除了微孔外还有一定量的中孔和大孔. 相似文献
819.
C. Nobre M.J. Santos D. Torres O. Rocha I. Rocha E.C. Ferreira L.R. Rodrigues 《Analytica chimica acta》2009,654(1):71-78
Adsorption equilibrium of fructose, glucose and sucrose was evaluated on sulfonated poly(styrene-co-divinylbenzene) cation-exchange resins. Two types of resins were used: potassium (K+) gel-type and sodium (Na+) macroporous resins. Influence of the cation and effect of the resin structure on adsorption were studied. The adsorption isotherms were determined by the static method in batch mode for mono-component and multi-component sugar mixtures, at 25 and 40 °C, in a range of concentrations between 5 and 250 g L−1. All adsorption isotherms were fitted by a linear model in this range of concentrations. Sugars were adsorbed in both resins by the following order: fructose > glucose > sucrose. Sucrose was more adsorbed in the Na+ macroporous resin, glucose was identically adsorbed, and fructose was more adsorbed in the K+ gel-type resin. Data obtained from the adsorption of multi-component mixtures as compared to the mono-component ones showed a competitive effect on the adsorption at 25 °C, and a synergetic effect at 40 °C. The temperature increase conducted to a decrease on the adsorption capacity for mono-component sugar mixtures, and to an increase for the multi-component mixtures. Based on the selectivity results, K+ gel-type resin seems to be the best choice for the separation of fructose, glucose and sucrose, at 25 °C. 相似文献
820.
Cs. Kotsmar V.S. Alahverdjieva E.V. Aksenenko V.I. Kovalchuk M.E. Leser R. Miller 《Advances in colloid and interface science》2009,150(1):41-54
Depending on the bulk composition, adsorption layers formed from mixed protein/surfactant solutions contain different amounts of protein. Clearly, increasing amounts of surfactant should decrease the amount of adsorbed proteins successively. However, due to the much larger adsorption energy, proteins are rather strongly bound to the interface and via competitive adsorption surfactants cannot easily displace proteins. A thermodynamic theory was developed recently which describes the composition of mixed protein/surfactant adsorption layers. This theory is based on models for the single compounds and allows a prognosis of the resulting mixed layers by using the characteristic parameters of the involved components. This thermodynamic theory serves also as the respective boundary condition for the dynamics of adsorption layers formed from mixed solutions and their dilational rheological behaviour. Based on experimental studies with milk proteins (β-casein and β-lactoglobulin) mixed with non-ionic (decyl and dodecyl dimethyl phosphine oxide) and ionic (sodium dodecyl sulphate and dodecyl trimethyl ammonium bromide) surfactants at the water/air and water/hexane interfaces, the potential of the theoretical tools is demonstrated.The displacement of pre-adsorbed proteins by subsequently added surfactant can be successfully studied by a special experimental technique based on a drop volume exchange. In this way the drop profile analysis can provide tensiometry and dilational rheology data (via drop oscillation experiments) for two adsorption routes — sequential adsorption of the single compounds in addition to the traditional simultaneous adsorption from a mixed solution. Complementary measurements of the surface shear rheology and the adsorption layer thickness via ellipsometry are added in order to support the proposed mechanisms drawn from tensiometry and dilational rheology, i.e. to show that the formation of mixed adsorption layer is based on a modification of the protein molecules via electrostatic (ionic) and/or hydrophobic interactions by the surfactant molecules and a competitive adsorption of the resulting complexes with the free, unbound surfactant. Under certain conditions, the properties of the sequentially formed layers differ from those formed simultaneously, which can be explained by the different locations of complex formation. 相似文献