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81.
Novel adsorbents which can concentrate Th(IV) in aqueous solution were prepared by immobilizingMyrica rubra tannin and larch tannin onto collagen fibre matrices. The adsorption capacities of the immobilized tannins to Th(IV) are
related to temperature and pH value of the adsorption process. For example, when the initial concentration of Th(IV) was 116.0
mg·l-1 and the immobilized tannin was 100 mg, the adsorption capacities of immobilized Myrica rubra tannin and larch tannin were 55.98 mg Th(IV)·g-1 and 13.19 mg Th(IV)·g-1, respectively at 303 K, and 73.67 mg Th(IV)·g-1 and 18.19 mg Th(IV)·g-1 at 323 K. It was also found that the higher adsorption capacity was obtained at higher pH value. The adsorption equilibrium
data of the immobilized tannins for Th(IV) can be well fitted by the Langmuir model and the mechanism of the adsorption was
found to be a chemical adsorption. In general, the adsorption capacity of immobilized Myrica rubra tannin to Th(IV) is significantly higher than that of immobilized larch tannin, probably due to the fact that the B ring
of Myrica rubra tannin has a pyrogallol structure which has higher reaction activity with metal ions. The breakthrough point of the adsorption
column of immobilized Myrica rubra tannin was at 33 bed volumes for the experimental system. The mass transfer coefficient of adsorption column determined by
Adams-Bohart equation was 1.61·10-4 l·mg-1.min-1. The adsorption column can be easily regenerated by 0.1 mol·l-1 HNO3 solution, showing outstanding ability of concentrating Th(IV).
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
82.
The hydrothermal reactions of AgNO(3), 4,4'-bipy, and carboxylate ligands gave rise to three supramolecular architectures, namely [Ag(bipy)].H(2)SIPA.1/2bipy.H(2)O (1), [Ag(bipy)].1/2H(2)btec.H(2)O (2), and [Ag(bipy)](2).H(2)dpstc.2H(2)O (3) (H(3)SIPA = 5-sulfoisophthalic acid, bipy = 4,4'-bipyridine, H(4)btec = 1,2,4,5-benzenetetracarboxylic acid, H(4)dpstc = 3,3',4,4'-tetracarboxydiphenyl sulfone). All complexes are extended from Ag-bipy linear chains by the combination of coordination bonds and supramolecular interactions in two different approaches. Complexes 1 and 3 comprise two-dimensional frameworks. In the two complexes, a one-dimensional ladderlike structure is first formed by the connection of a Ag-bipy chain through hydrogen bonding between a free carboxylate/bipy ligand and weak coordinative interactions between a free carboxylate ligand and silver ion. The ladderlike structure is then extended to a two-dimensional layer architecture by pi...pi interactions between bipy ligands of the Ag-bipy chains. Complex 2 possesses a three-dimensional framework. The free H(2)btec(2)(-) ligands form a two-dimensional layer network by hydrogen-bonding interactions between protonated and deprotonated carboxylate groups; meanwhile, pi.pi interactions between bipy ligands of Ag-bipy chains also result in a two-dimensional layer. The two layers are further connected by weak Ag-O interactions to generate a three-dimensional supramolecular structure. 相似文献
83.
Jianxing Bi 《数学学报(英文版)》1995,11(3):300-306
LetG be a finite group. If
for every primer, whereR
1 Syl
r
G andR
2 Syl
r
(L
n
(q)), thenG L
n
(q). 相似文献
84.
J. N. Spencer Jarusha DeGarmo I. M. Paul Qing He Xiaoming Ke Zhenqing Wu C. H. Yoder Shuyun Chen J. E. Mihalick 《Journal of solution chemistry》1995,24(6):601-609
Calorimetric studies of the inclusion complexes of straight and branched alcohols and of diols with alpha-cyclodextrin (-CD) have been carried out in water solvent. The data suggest that straight and branched chain alcohols enter the cavity of -CD alkyl end first. The hydroxyl group hydrogen bonds to the outer oxygen ring of the cyclodextrin. For branched chain alcohols the longer alkyl part of the molecule penetrates the -CD cavity up to the hydroxyl group. Diols form two hydrogen bonds to the outer oxygen ring of the cyclodextrin with some penetration into its interior. 相似文献
85.
86.
相转移催化氧化合成苯甲酸 总被引:1,自引:0,他引:1
苯甲酸一般由甲苯氧化而成 ,工业上采用液相空气氧化生产苯甲酸[1 ] 。KMnO4氧化甲苯制备苯甲酸的方法是在实验室中最常见的一种方法[2 ] ,该法的优点是反应条件温和 ,操作简便 ;其缺点是反应时间长 ,产率低 (低于 40 % ) [3] 。为了提高KMnO4氧化法的产率 ,本文采用十六烷基三丁基溴化磷 (HDTBP)和苄基三乙基氯化铵(BTEA)作相转移催化剂氧化甲苯制备苯甲酸 ,具有时间短 ,收率高等优点。同时又考虑到HDTBP的催化效果虽然好 ,但价格昂贵 ,因此本文采用价廉易得的苄基三乙基氯化铵 (BTEA)作相转移催化剂氧化甲苯制… 相似文献
87.
Eu(Ⅲ)、Tb(Ⅲ)、Ho(Ⅲ)、Tm(Ⅲ)和Lu(Ⅲ)与N,N′-二(邻羟基亚甲基)乙二胺配合物的研究 总被引:1,自引:0,他引:1
Dutt曾合成稀土离子与N,N′-二(邻羟基亚甲基)乙二胺的稀土双希夫碱配合物。但未见报道Eu(Ⅲ),Tb(Ⅲ),Ho(Ⅲ),Tm(Ⅲ),Lu(Ⅲ)与双希夫碱N,N′-二(邻羟基亚甲基)乙二胺的配合物。本工作合成了这5种双希夫碱配合物。 所用稀土氧化物纯度大于99.9%(上海跃龙化工厂)。水杨醛(CP,用前经减压蒸馏提纯)。稀土硝酸盐Ln(NO_3)_3·xH_2_由稀土氧化物与硝酸反应制得。其余试剂均为分析纯。 仪器为Perkin-Elmer 240-C元素分析仪;Nicolet-5DX型红外光谱仪,KBr压片;岛津UV- 相似文献
88.
汞电极表面电荷的快速估算 总被引:1,自引:0,他引:1
本文报导了用交流示波极谱快速估算电极表面电荷的方法。该方法使用仪器简单,测量快速,操作简便,在吸附研究中很有用处。 相似文献
89.
Ren Xiaoming Wu Peiheng Zhang Wenwei Meng Qingjin Chen Xiaoyuan 《Transition Metal Chemistry》2002,27(4):394-397
Ion-pair complexes consisting of the [Fe(mnt)2]– anion and [RBzPy]+ cations [R = NO2
(1) or Cl (2)] have been prepared and characterized by elemental analysis and i.r. spectroscopy. The single crystal structure of (1) shows that the [Fe(mnt)2]– anions are dimeric, and that the coordination geometry of each Fe atom is square pyramidal. The most significant structural feature of (1) is that anions and cations form completely separate columns and – interactions occur within the cation columns. Thermal variations of
m
T for the complexes indicated antiferromagnetic coupling within the dimer. 相似文献
90.
在理学3064X荧光仪上采用十八烷基马来酸(OHM)晶体作为色散单元,通过改造电路,调整晶体倾角,获得对碳分析的良好线性,在流气正比计数器(FPC)窗膜分别为5μm和0.6μm条件下,碳元素的峰背比分别达到38.91和54.04。作者分析了白口铸铁和碳化硅中的碳,结果表明在理学3064X荧光仪上定量分析碳是可行了,具有快速、简便、准确、多元素同时分析的特点,可用于日常分析 相似文献