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481.
Baozhen Wang 《Talanta》2007,72(2):415-418
Multilayer thin films composed of poly(allylamine hydrochloride) (PAH) and carboxymethyl cellulose (CMC) have been prepared on the surface of a gold (Au) disk electrode by a layer-by-layer deposition of PAH and CMC and ferricyanide ions ([Fe(CN)6]3−) were confined in the film. [Fe(CN)6]3− ions can be successfully confined in the films from weakly acidic or neutral [Fe(CN)6]3− solutions, while, in basic solution, [Fe(CN)6]3− ion was not confined. The [Fe(CN)6]3− ion-confined Au electrode showed clear redox peaks in the cyclic voltammogram around 0.35 V versus Ag/AgCl. The amounts of [Fe(CN)6]3− ions confined in the films depended on the thickness of the films or the number of layers in the LbL films. The [Fe(CN)6]3− ion-confined Au electrode was used for electrocatalytic determination of ascorbic acid in the concentration range of 1-50 mM. 相似文献
482.
A glassy carbon electrode (GCE) was modified with electropolymerized films of isonicotinic acid in pH 5.6 phosphate buffer solution (PBS) by cyclic voltammetry (CV). The modified electrode showed an excellent electrocatalytical effect on the oxidation of norepinephrine (NE). In PBS of pH 7.4, the oxidation current increased linearly with two concentration intervals of NE, one is 4.0×10−7 to 1.0×10−5 M, the other is 1.0×10−5 to 2.0×10−4 M. The detection limit (S/N=3) obtained by DPV was 6.0×10−9 M. Then the modified electrode was used to determine NE in an excess of ascorbic acid (AA) by difference pulse voltammetry. The peak potentials recorded in a PBS of pH 7.4 were −68 and +111 mV versus SCE for AA and NE, respectively. The high selectivity and sensitivity for NE was found to be due to the very distinct attracting interaction between NE cations and the negtively charged poly(isonicotinic acid) film in pH 7.4 PBS. The proposed method exhibited good recovery and reproducibility. 相似文献
483.
Lei Qian Xiurong Yang 《Colloids and surfaces. A, Physicochemical and engineering aspects》2005,260(1-3):79-85
Ag(Au) bimetallic core–shell nanoparticles were prepared by a new seed growth method. Ascorbic acid was used to reduce the complex of HAuCl4 and hexadecyltrimethylammoniumbromide (CTAB). This resulted in the forming of colorless Au(I) (AuCl2−). It was used as the growth solution to prepare these bimetallic core–shell nanoparticles. These nanoparticles were characterized by UV–vis spectroscopy, transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The results showed these nanoparticles exhibited core–shell shape and there was large amount of Ag in the shell. These nanoparticles could be produced in a few minutes without violent stirring and the method was easy and convenient compared with others. The effect of amount of AuCl2− on the shape of nanoparticles was also studied. Many small gold nanoparticles were formed on the surface of bimetallic core–shell nanoparticles in the presence of excess AuCl2−. The mechanisms were also proposed to explain the process of colloidal preparation. 相似文献
484.
聚苯胺薄膜修饰电极对抗坏血酸的电催化氧化 总被引:12,自引:0,他引:12
本文表明聚苯胺(PAn)薄膜修饰电极对水溶液中的抗坏血酸(AH_2)在较宽的pH范围和较宽的浓度范围内均有良好的电催化氧化作用, 为EC平行催化过程。利用旋转圆盘电极(RDE)进行了催化过程动力学分析, 求出了催化反应动力学参数。在抗坏血酸浓度10~(-2)~10~(-6) mol·L~(-1)范围内, 催化峰电流与AH_2浓度均成良好的线性关系, 且PAn薄膜修饰电极具有很好的稳定性, 有应用分析抗坏血酸的意义。 相似文献
485.
Cadmium in polyethylene was determined by both inductively coupled plasma atomic emission spectrometry (ICP-AES) and atomic absorption spectrometry (AAS) with continuous-flow gas-phase sample introduction in a reaction medium of ascorbic acid. In the presence of mixture of cobalt and thiourea in the ascorbic acid solution, the sensitivities by both ICP-AES and AAS for cadmium were greatly enhanced. The gaseous cadmium species was phase-separated in a gas–liquid separator and directed via a stream of argon carrier gas to an inductively coupled plasma and an electrically heated quartz tube atomizer (QTA) for atomic spectrometry. Under the optimized experimental conditions, the best attainable detection limits at Cd I 228.802 nm line were 1.3 and 0.017 ng/ml with linear dynamic ranges of 10–500 ng/ml and 0.1–1 ng/ml in concentrations by ICP-AES and QTA-AAS, respectively. The instrumental precisions expressed as the relative standard deviation (R.S.D.) from ten replicate measurements of 50 and 1 ng/ml cadmium by ICP-AES and QTA-AAS were 5.6% and 3.2%, respectively. With the use of ICP-AES and QTA-AAS with gas-phase sample introduction method, six- and 200-fold improvements in detection limits for cadmium were obtained in comparison with their conventional solution nebulization methods, respectively. After the effects of several diverse elements on the determination of cadmium by ICP-AES and QTA-AAS with the present gas-phase sample introduction systems were examined, these methods were applied to the determination of low concentrations of cadmium in polyethylene. The results obtained by the present method were in good agreement with the certified values. 相似文献
486.
New methylene blue (NMB) dye incorporated into AlMCM‐41 surfactant‐free and hybrid surfactant‐AlMCM‐41 mesophase. UV‐vis evidence shows that new methylene blue dye protonated in both cases of zeolites. New methylene blue is electroactive in zeolites and their electrochemical activity has been studied by cyclic voltammetry and compared to that of NMB in aqueous solutions. New methylene blue molecules are not released to the solution during CV measurements and are accessible to H3O+ ions. The presence of surfactant affects the kinetics of the redox process through proton ions diffusion. The midpoint potentials (Em) values show that new methylene blue dye incorporated into AlMCM‐41 can be reduced easily with respect to solution new methylene blue. New methylene blue interacting with surfactant polar heads and residual Br? ions as a results, it shows a couple of peaks in high potential with respect to new methylene blue solution. The electrode made with methylene blue‐AlMCM‐41 without surfactant was used for the mediated oxidation of ascorbic acid. The anodic peak current observed in cyclic voltammetry was linearly dependent on the ascorbic acid concentration. The calibration plot was linear over the ascorbic acid concentration range 1.0×10?5 to 5.0×10?4 M. The detection limit of the method is 1.0×10?5 M, low enough for trace ascorbic acid determination in various real samples. 相似文献
487.
P. Ortega Barrales M. L. Fernndez de Crdova A. Molina Díaz 《Analytica chimica acta》1998,360(1-3):143-152
Solid-phase spectrophotometry (SPS) technique, in the visible region, was used for the spectrophotometric determination of ascorbic acid based on the reducing effect on iron(III) ion, followed by formation of the iron(II)-ferrozine chelate. The chelate is easily sorbed on a dextran-type anion-exchange gel and the absorbance of the resin at 567 and 800 nm, packed in a 1 mm cell, is measured directly. The apparent molar absorptivity using 100 ml of sample was 2.1×107 l mol−1 cm−1 and it allowed the determination of ascorbic acid in the range 5–90 ng ml−1; the detection limit was 0.91 ng ml−1 and the RSD 0.91% for a concentration of 50 ng ml−1 of ascorbic acid (n=10). The proposed method permits a highly sensitive and selective determination of ascorbic acid without any preconcentration and it has been satisfactorily applied for its determination in fruit juices, pharmaceuticals, urine and conservative liquids. 相似文献
488.
489.
制备了聚乙烯亚胺(PEI)功能化的石墨烯(G)修饰电极以实现抗坏血酸(AA)、 多巴胺(DA)、 尿酸(UA)和色氨酸(Trp)的分离及同时测定. 采用红外光谱(FTIR)、 紫外-可见吸收光谱(UV-Vis)、 X射线粉末衍射仪(XRD)和透射电子显微镜(TEM)对电极修饰材料进行了表征, 并优化了该修饰电极同时测定AA, DA, UA和Trp的实验条件. 在聚乙烯亚胺功能化石墨烯修饰的玻碳电极(PEI-G/GCE)上实现了AA, DA, UA 和Trp氧化峰的分离, AA-DA, DA-UA和UA-Trp的氧化峰电位差分别为298, 130和350 mV. 该修饰电极对AA, DA, UA和Trp的检测线性范围分别为50~5800, 30~2570, 0.05~400和6~1000 μmol/L; 检出限分别为16.67, 10, 0.017和2 μmol/L. 相似文献
490.