首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   48篇
  免费   3篇
  国内免费   2篇
化学   28篇
数学   12篇
物理学   13篇
  2022年   1篇
  2021年   1篇
  2020年   2篇
  2018年   1篇
  2016年   1篇
  2015年   1篇
  2014年   10篇
  2013年   3篇
  2012年   6篇
  2011年   5篇
  2010年   1篇
  2009年   2篇
  2008年   2篇
  2006年   1篇
  2005年   2篇
  2004年   1篇
  2002年   2篇
  2001年   2篇
  1999年   5篇
  1998年   1篇
  1996年   1篇
  1994年   1篇
  1993年   1篇
排序方式: 共有53条查询结果,搜索用时 31 毫秒
41.
For the first time, the electrochemical synthesis of gold nanostructures was done at the surface of carbon paste electrode. This device was used as a simple and sensitive electrochemical sensor for measurement of pyridoxine (Vitamin B6, VB6). The diffusion coefficient (D) and the kinetic parameters such as electron transfer coefficient (α) and catalytic rate constant (k) for VB6 were also determined using electrochemical approaches. The cyclic voltammetry method showed VB6 oxidation reaction with irreversible characteristics was diffusion-controlled at low scan rates. Using differential pulse voltammetry (DPV), the peak current was linearly dependent on VB6 concentration in the ranges of 1.9–110.8 and 110.8–257.0 μM, with detection limit of 74.0 nM, respectively. Results showed there is no interference of other vitamins in oxidation of VB6. DPV was used to quantify of VB6 in some real samples by the standard addition method. The modified electrode showed good sensitivity and stability.  相似文献   
42.
In this study inclusion of hexadecyltrimethylammonium bromide (HTAB) with α-, and β-cyclodextrin (CD) in the presence and the absence of bromhexine (BH) was investigated using ion-selective electrode method. The association constants of HTAB with CDs were determined by potentiometry and were close to literature values. The obtained results indicated that α-CD formed 1:1 and 1:2 inclusion complexes, but β-CD formed only a 1:1 inclusion complex. In the presence of drug, the interaction between CDs and HTAB decreased, because both drug and HTAB could interact with CDs. The results showed that the interaction between drug and CDs are greater than HTAB and CDs. The stoichiometry of the inclusion complexes, the critical aggregation concentration (CAC), the monomer surfactant concentration of HTAB, [HTAB]f, and also the effect of the inclusion complex on the micellization process of the HTAB were determined by conductivity measurements.  相似文献   
43.
A new preconditioning method is investigated to reduce the roundoff error in computing derivatives using Chebyshev collocation methods(CCM). Using this preconditioning causes ratio of roundoff error of preconditioning method and CCM becomes small when N gets large. Also for accuracy enhancement of differentiation we use a domain decomposition approach. Error analysis shows that for this domain decomposition method error reduces proportional to the length of subintervals. Numerical results show that using domain decomposition and preconditioning simultaneously, gives super accurate approximate values for first derivative of the function and good approximate values for moderately high derivatives.  相似文献   
44.
A method based on ESI ion mobility spectrometry as a detection technique after treatment with a molecularly imprinted polymer is described for the analysis of pioglitazone. In addition to the molecularly imprinted polymer separation methodology, the positive ion mobility spectrum and the reduced mobility values for pioglitazone are reported for the first time. The method was exhaustively validated in terms of sensitivity, imprinting factor, enrichment factor, and sorption capacity. A linear dynamic range of 0.10–20.00 μg/mL and an RSD below 6% were obtained for the analysis of this compound. The average recovery for the analysis of spiked samples was calculated to be about 91%. The method was also used to determine pioglitazone in cow plasma, and the results were compared with those obtained using HPLC. The satisfactory results evidence a convenient method for the analysis of the target compound in real samples without using any additional derivatization methods.  相似文献   
45.
46.
47.
Two new 2 : 1 co‐crystals based on [4,4′‐bithiazole]‐2,2′‐diamine (=2,2′‐diamino‐4,4′‐bithiazole (DABTZ)) with 2,2′‐bipyridine (bipy) and benzo‐18‐crown‐6 (bk) were synthesized by slow‐evaporation method in MeOH. These co‐crystals were characterized by means of elemental analysis, and IR, and 1H‐ and 13C‐NMR spectroscopy. Also, thermal analyses under air atmosphere and X‐ray crystallography have been performed on these structures. X‐Ray single‐crystal analyses revealed that these networks contain large vacant voids. These structures, [(DABTZ)2(bipy)] and [(DABTZ)2(bk)(MeOH)], crystallized in monoclinic and triclinic forms with space groups of P21/c and P , respectively. The self‐assembly of these compounds in the solid state is likely caused by both H‐bonding and π? π stacking.  相似文献   
48.
To avoid an enormous energy crisis in the not-too-distant future, it be emergent to establish high-performance energy storage devices such as supercapacitors. For this purpose, a three-dimensional (3D) heterostructure of Co3O4 and Co3S4 on nickel foam (NF) that is covered by reduced graphene oxide (rGO) has been prepared by following a facile multistep method. At first, rGO nanosheets are deposited on NF under mild hydrothermal conditions to increase the surface area. Subsequently, nanowalls of cobalt oxide are electro-deposited on rGO/Ni foam by applying cyclic-voltammetry (CV) under optimized conditions. Finally, for the synthesis of Co3O4@Co3S4 nanocomposite, the nanostructure of Co3S4 was fabricated from Co3O4 nanowalls on rGO/NF by following an ordinary hydrothermal process through the sulfurization for the electrochemical application. The samples are characterized by using X-ray diffraction (XRD) and scanning electron microscopy (SEM). The obtained sample delivers a high capacitance of 13.34 F cm−2 (5651.24 F g−1) at a current density of 6 mA cm−2 compared to the Co3O4/rGO/NF electrode with a capacitance of 3.06 F cm−2 (1230.77 F g−1) at the same current density. The proposed electrode illustrates the superior electrochemical performance such as excellent specific energy density of 85.68 W h Kg−1, specific power density of 6048.03 W kg−1 and a superior cycling performance (86% after 1000 charge/discharge cycles at a scan rate of 5 mV s−1). Finally, by using Co3O4 @Co3S4/rGO/NF and the activated carbon-based electrode as positive and negative electrodes, respectively, an asymmetric supercapacitor (ASC) device was assembled. The fabricated ASC provides an appropriate specific capacitance of 79.15 mF cm−2 at the applied current density of 1 mA cm−2, and delivered an energy density of 0.143 Wh kg−1 at the power density of 5.42 W kg−1.  相似文献   
49.
In this work, we investigate the electrochemical activity of dopamine (DA) and uric acid (UA) using both a bare and a modified carbon paste electrode as the working electrode, with a platinum wire as the counter electrode and a silver/silver chloride (Ag/AgCl) as the reference electrode. The modified carbon paste electrode consists of multi-walled carbon nanotubes (>95%) treated with α-cyclodextrine, resulting in an electrode that exhibits a significant catalytic effect toward the electro-chemical oxidation of DA in a 0.2-M Britton–Robinson buffer solution (pH 5.0). The peak current increases linearly with the DA concentration within the molar concentration ranges of 2.0 × 10−6 to 5.0 × 10−5 M and 5.0 × 10−5 to 1.9 × 10−4 M. The detection limit (signal to noise >3) for DA was found to be 1.34 × 10−7 M, respectively. In this work, voltammetric methods such as cyclic voltammetry, chronoamperometry, chronocuolometry, differential pulse and square wave voltammetry, and linear sweep and hydrodynamic voltammetry were used. Cyclic voltammetry was used to investigate the redox properties of the modified electrode at various scan rates. The diffusion coefficient (D, cm2 s−1 = 3.05 × 10−5) and the kinetic parameters such as the electron transfer coefficient (α = 0.51) and the rate constant (k, cm3 mol−1 s−1 = 1.8 × 103) for DA were determined using electrochemical approaches. By using differential pulse voltammetry for simultaneous measurements, we obtained two peaks for DA and UA in the same solution, with the peak separation approximately 136 mV. The average recovery was measured at 102.45% for DA injection.  相似文献   
50.
Maximizing nonlinear light-matter interactions is a primary motive for compressing laser pulses to achieve ultrashort transform limited pulses. Here we show how, by appropriately shaping the pulses, resonant multiphoton transitions can be enhanced significantly beyond the level achieved by maximizing the pulse's peak intensity. We demonstrate the counterintuitive nature of this effect with an experiment in a resonant two-photon absorption, in which, by selectively removing certain spectral bands, the peak intensity of the pulse is reduced by a factor of 40, yet the absorption rate is doubled. Furthermore, by suitably designing the spectral phase of the pulse, we increase the absorption rate by a factor of 7.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号