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51.
We prove a new Bailey-type transformation relating WP-Bailey pairs. We then use this transformation to derive a number of new 3- and 4-term transformation formulae between basic hypergeometric series.  相似文献   
52.
   Abstract. We give an r -dimensional generalization of H. S. Shukla's very-well-poised 8 ψ 8 summation formula. We work in the setting of multiple basic hypergeometric series very-well-poised over the root system A r-1 or, equivalently, the unitary group U(r) . Our proof, which is already new in the one-dimensional case, utilizes an A r-1 nonterminating very-well-poised 6 φ 5 summation by S. C. Milne, a partial fraction decomposition, and analytic continuation.  相似文献   
53.
We give some necessary and sufficient conditions which completely characterize the strong and total Lagrange duality, respectively, for convex optimization problems in separated locally convex spaces. We also prove similar statements for the problems obtained by perturbing the objective functions of the primal problems by arbitrary linear functionals. In the particular case when we deal with convex optimization problems having infinitely many convex inequalities as constraints the conditions we work with turn into the so-called Farkas-Minkowski and locally Farkas-Minkowski conditions for systems of convex inequalities, recently used in the literature. Moreover, we show that our new results extend some existing ones in the literature.  相似文献   
54.
丙二醇醚类化合物是性能优良的精细化学品,也是环保型高级溶剂.该类化合物具有两个强溶解性功能基团—醚键和羟基,前者具有亲油性,可溶解疏水性物质,后者具有亲水性,可溶解亲水性物质,因而丙二醇醚具有很强的溶解能力,素有"万能溶剂"之称,可广泛应用于涂料、油墨、油漆、印刷、电子化学品、染料、净洗和纺织等行业.丙二醇醚类化合物目前主要由环氧丙烷和低级脂肪醇反应合成,然而,由于环氧丙烷的位阻效应,使其在酸或碱的条件下开环的位置会不同,从而得到不同的醇醚产物.由于碱催化的醇醚产物更加环境友好,因而越来越被人们所关注.工业上丙二醇醚合成多采用传统的强碱性催化剂醇钠以及氢氧化钠,腐蚀性强,产生的废液量大.本文采用环境友好的非卤素离子液体作为催化剂,研究了其催化环氧丙烷醚化合成丙二醇醚的反应特性.本文采用两步法合成了一系列环境友好的醋酸类碱性功能化离子液体,并在温和的条件下将其用于催化环氧丙烷与醇反应合成丙二醇醚.结果表明,该类离子液体可以高效催化该反应的进行.利用紫外-可见光谱测定Hammett指数来表征实验中所用离子液体的碱强度,并构建了离子液体碱性与催化活性之间的关系.结果表明,离子液体的催化性能和其碱性密切相关,随着离子液体碱性的增加,催化活性增强,其中咪唑醋酸类离子液体碱性强于季胺类,表现出优异的催化性能.离子液体的碱性明显弱于NaOH,但却呈现出更优异的催化性能.相同反应条件下,EmimOAc离子液体作为催化剂,PO的转化率分别较NaOH高出20%–30%,选择性略高于NaOH,这可能是由于二者催化机理不同造成的.传统NaOH催化机理的关键步骤是醇在碱性催化剂的作用下去质子化形成电子供体烷氧根离子,促进环氧丙烷的开环加成.而本文提出了离子液体亲电亲核双活化作用机理,即离子液体在阴阳离子之间的氢键和电荷相互作用的共同作用下,促进环氧丙烷开环和醇的去质子化,形成相应的反应中间体.通过电喷雾质谱分析手段检测到了阴阳离子通过协同作用亲电亲核催化过程中的反应中间体,证明了该假设机理的可行性.此外,还考察了催化剂浓度、醇比、反应温度以及醇的空间位阻效应对反应的影响.以EmimOAc催化合成丙二醇丁醚为例,反应的转化率随催化剂浓度的增加而增大,在催化剂添加量1%(催化剂与PO的摩尔比)时,PO转化率达到最大值为98.2%,1-丁氧基-2-丙醇的选择性为86.4%.当正丁醇与环氧丙烷的摩尔比为3时,转化率最高为88.6%,选择性高达94%.该反应为放热反应,最适反应温度约为140 oC,此时转化率高达96.5%.在环氧丙烷和不同的低碳醇合成丙二醇醚的反应中,反应物醇的碳链越短,支链越少,催化反应效率越高.  相似文献   
55.
The effectiveness of several basic compounds for testing silica‐based stationary phases was reviewed by applying them to recent columns for reversed‐phase HPLC. Most octadecylsilylated (C18) stationary phases, prepared as a base‐deactivated material from high‐purity silica gel with endcapping, provided excellent peak shape and column efficiency for the bases including benzylamine and amitriptyline that once caused problems and were subsequently employed for testing silanol activities. However, a cyclic tertiary amine, dextrometorphan, was eluted as an acceptable peak from only a few columns at neutral pH. Such a more sensitive probe is expected to contribute to further improvement of the stationary phase for reversed‐phase HPLC.  相似文献   
56.
Spermine-graft-dextran (Spe-g-Dex) copolymer was synthesized and used as a non-covalent coating for the separation of proteins and neurotransmitters by capillary electrophoresis. The coating was obtained via flushing the capillary with 1.0% Spe-g-Dex copolymer solution for 2 min. Electroosmotic flow (EOF) was strongly suppressed, ranging from −1.60 × 10−9 to 3.65 × 10−9 m2 V−1 s−1. Effect of experimental conditions, such as the copolymer concentration, the concentration and pH of the background electrolyte (BGE), on the Spe-g-Dex coating was investigated. Separation of lysozyme, cytochrome c, ribonuclease A and α-chymotrypsinogen yielded high separation efficiencies ranging from 141 000 to 303 000 plates/m and recoveries from 85.4% to 98.3% at pH 4.0 (284.0 mM sodium acetate–acetic acid buffer, I = 50 mM). Run-to-run repeatabilities and day-to-day, and capillary-to-capillary reproducibilities were all below 1.7%. In addition, Spe-g-Dex coating allowed the successful separation of five neurotransmitters, 5-hydroxytryptamine, dopamine, epinephrine, isoprenaline, dobuamine at pH 4.0 with high separation efficiencies of 290 000–449 000 plates/m.  相似文献   
57.
Zhou S  Tan J  Chen Q  Lin X  Lü H  Xie Z 《Journal of chromatography. A》2010,1217(52):8346-8351
A novel open tubular (OT) column covalently modified with hydrophilic polysaccharide, carboxymethylchitosan (CMC) as stationary phase has been developed, and employed for the separations of basic proteins and opium alkaloids by capillary electrochromatography (CEC). With the procedures including the silanization of 3-aminopropyltrimethoxysilane (APTS) and the combination of glutaraldehyde with amino-silylated silica surface and CMC, CMC was covalently bonded on the capillary inner wall and exhibited a remarkable tolerance and chemical stability against 0.1 mol/L HCl, 0.1 mol/L NaOH or some organic solvents. By varying the pH values of running buffer, a cathodic or anodic EOF could be gained in CMC modified column. With anodic EOF mode (pH<4.3), favorable separations of basic proteins (trypsin, ribonuclease A, lysozyme and cytochrome C) were successfully achieved with high column efficiencies ranging from 97,000 to 182,000 plates/m, and the undesired adsorptions of basic proteins on the inter-wall of capillary could be avoided. Good repeatability was gained with RSD of the migration time less than 1.3% for run-to-run (n=5) and less than 3.2% for day-to-day (n=3), RSD of peak area was less than 5.6% for run-to-run (n=5) and less than 8.8% for day-to-day (n=3). With cathodic EOF mode (pH>4.3), four opium alkaloids were also baseline separated in phosphate buffer (50 mmol/L, pH 6.0) with column efficiencies ranging from 92,000 to 132,000 plates/m. CMC-bonded OT capillary column might be used as an alternative medium for the further analysis of basic proteins and alkaline analytes.  相似文献   
58.
采用反相悬浮聚合法制备了甲基丙烯酸羟乙酯(HEMA)与N-乙烯基吡咯烷酮(NVP)的交联共聚微球HEMA/NVP,然后采用"接出"法,实施了甲基丙烯酸(MAA)在交联微球表面的接枝聚合,制得了接枝微球PMAA-HEMA/NVP.以溶菌酶(LYZ)为模型碱性蛋白,深入研究了接枝微球PMAA-HEMA/NVP对碱性蛋白的吸附性能与吸附机理.测定了微球PMAA-HEMA/NVP的zeta电位,考察了PMAA接枝度、介质pH值及离子强度等因素对体系吸附性能的影响.结果表明,在较大的pH范围内,接枝微球PMAA-HEMA/NVP的zeta电位为绝对值较大的负值,即其表面携带有高密度的负电荷.在强静电相互作用的驱动下,接枝微球PMAA-HEMA/NVP对溶菌酶表现出很强的吸附能力.随介质pH值的增高,接枝微球对溶菌酶的吸附容量呈现先增大后减小的变化趋势,在与溶菌酶等电点接近的pH值处(pH=9),具有最大的吸附容量(90mg.g-1);离子强度对接枝微球的吸附能力也有较大的影响,当pH9时,溶菌酶吸附容量随NaCl浓度的增高而减小;当pH9时,吸附容量随NaCl浓度的增高而增大.  相似文献   
59.
掺Fe3+A-TiO2粉末的制备及其可见光催化降解碱性品红   总被引:1,自引:0,他引:1  
张一兵  肖朵朵  江雷 《光谱实验室》2011,28(4):1667-1671
以硫酸钛为原料用水热法制备了掺Fe3+TiO2粉末,用SEM测定了样品的形貌和晶型,研究了以自制的掺Fe3+ A-TiO2对碱性品红溶液的光催化降解作用.结果表明:所制备的TiO2为锐铁矿型TiO2(A-TiO2).可见光照射下,用自制的掺Fe3+A-TiO2降解碱性品红溶液的最佳条件是:2mg·L-1的碱性品红溶液中...  相似文献   
60.
The visual secret sharing for multiple secrets (VSSM) allows for the encryption of a greater number of secret images into a given image area. Previous researches on VSSM schemes incur a very serious pixel expansion that will damage capable of increasing the capacity of secret image encryption. Moreover, the most of VSSM schemes will decrease the contrast of recover images while the amount of secret image encryption increases. These drawbacks limit applicability of the existing VSSM schemes. In this paper, we propose a highly efficient encryption algorithm to cope with this problem. The proposed algorithm adopts a novel hybrid encryption approach that includes a VC-based encryption and a camouflaging process. The experimental results demonstrate that the proposed approach not only can increase the capacity efficient for VSSM schemes, but also maintains an excellent level of contrast in the recovered secret images.  相似文献   
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