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91.
本文阐述了Flash cs3 AcdonScript课件的优势及如何利用Flashcs3中具有的强大编程功能的AetionScript脚本语言制作大学物理CAI课件。 相似文献
92.
Wang Zhenya Chen Hui Yao Ligang Chen Xu Qi Xiaoli Zhang Jun 《Nonlinear dynamics》2021,106(3):2107-2130
Nonlinear Dynamics - Fault diagnosis of critical rotating machinery components is necessary to ensure safe operation. However, the commonly used rotating machinery fault diagnosis methods are... 相似文献
93.
The Soreq Applied Research Accelerator Facility (SARAF): Overview,research programs and future plans
Israel Mardor Ofer Aviv Marilena Avrigeanu Dan Berkovits Adi Dahan Timo Dickel Ilan Eliyahu Moshe Gai Inbal Gavish-Segev Shlomi Halfon Michael Hass Tsviki Hirsh Boaz Kaiser Daniel Kijel Arik Kreisel Yonatan Mishnayot Ish Mukul Ben Ohayon Michael Paul Amichay Perry Hitesh Rahangdale Jacob Rodnizki Guy Ron Revital Sasson-Zukran Asher Shor Ido Silverman Moshe Tessler Sergey Vaintraub Leo Weissman 《The European Physical Journal A - Hadrons and Nuclei》2018,54(5):91
94.
本文提出了对于手性药物普萘洛尔手性识别和手性分析的新方法。 该方法引用基于氧化石墨烯的指数富集配体系统进化筛选技术(GO-SELEX),经过10轮优化筛选出对心血管药物普萘洛尔有高度亲和力的特效适配体。 然后通过共振瑞利散射光谱法(RRS)对反应体系进行特效性检测,实验表明S-普萘洛尔和R-普萘洛尔有迥然不同的光谱差异,S-普萘洛尔与特效适配体结合后的RRS显著增强,而R-普萘洛尔与适配体结合后的RRS几乎没有变化。 据此可以对心血管药物手性普萘洛尔进行有效的手性识别。 在考察反应体系和实验条件的基础上,可对S-普萘洛尔进行实验检测,同时对外消旋体中的R-普萘洛尔进行计算分析。 实验对S-普萘洛尔的线性范围为5~275 nmol/L,检测限为0.5 nmol/L。 方法应用于外消旋药片的分析检测,结果令人满意。 实验表明,RRS检测特效适配体结合的手性靶标体系会彰显不同的光谱差异,从而可对手性对映体进行手性识别,尤其是可利用其光谱差异实现同时测定的手性分析,方法可在特殊情形下不经分离而同时测定手性对映体,具有推广应用价值。 相似文献
95.
Fabricating nitrogen-doped carbon layers over the conductive substrate is a cost-effective and efficient approach to develop practical oxygen reduction reaction (ORR) catalyst. In the current work, relying on the commercially available carbon nanotube (CNT), nitrogen-doped carbon layers over CNT is constructed by annealing the in situ formed complex over the CNT surface derived from iron ion inducing diaminonaphthalene (DAN) polymerization and DAN self-polymerization. Physical and electrochemical characterizations are carefully conducted to comparatively analyze the structure and activity relationship. The significance of iron in constructing nitrogen-doped carbon layers and tuning active sites of N types over multiwall carbon nanotube for ORR is demonstrated by X-ray photoelectron spectroscopy and Raman scattering spectrum. The excellent performance of nitrogen-doped carbon layers over CNT (catalyzed by iron) towards ORR is displayed by rotating ring-disk electrode. Specifically, the onset potential, half-wave potential, and limiting current density are 0.961 V, 0.831 V, and 5.20 mA cm?2 respectively, very close to the state-of-the-art commercial Pt/C catalyst. Both high surface area and efficient N active sites should be considered in the nitrogen-doped carbon materials design and fabrication for ORR. Considering the large-scale availability, it has significant value in fuel cells commercial applications. 相似文献
96.
Man Yan Ren Junan Li Bingru Jin Xinxin Pan Ligang 《Analytical and bioanalytical chemistry》2018,410(28):7511-7521
Analytical and Bioanalytical Chemistry - Alternariol monomethyl ether (AME) is one of the major Alternaria mycotoxins present in a wide range of fruits, vegetables, grains, and their products, and... 相似文献
97.
Qingqing Gai Qiuye Liu Wenyou Li Xiwen He Langxing Chen Yukui Zhang 《Frontiers of Chemistry in China》2008,3(4):370-377
Molecularly imprinted polymers (MIPs), based on photografting surface-modified polystyrene beads as matrices, were prepared
with acrylamide as the functional monomer, bovine hemoglobin as the template molecule and N, N′-methylene bisacrylamide as the crosslinker in a phosphate buffer. The results of IR, scanning electron microscope (SEM)
and elemental analyses demonstrated the formation of a grafting polymer layer on the polystyrene-bead surface. Subsequent
removal of the template left behind cavities on the surface of the polymer matrix with a shape and an arrangement of functional
groups having complementary binding sites with the original template molecule. The adsorption studies showed that the imprinted
polymers have a good adsorption capacity and specific recognition for bovine hemoglobin as the template molecule. Our results
demonstrated that the polymer prepared via the photografting surface-modified method exhibited better selectivity for the
template. Attempts to employ the new method in molecular imprinting techniques may introduce new applications for MIPs and
facilitate probable protein separation and purification.
__________
Translated from Chemical Journal of Chinese Universities, 2008, 29(1): 64–70 相似文献
98.
Gaião Eda N dos Santos SR dos Santos VB do Nascimento EC Lima RS de Araújo MC 《Talanta》2008,75(3):792-796
A microcontrolled, portable and inexpensive photometer is proposed. It uses a near infrared light emitting diode (NIR LED) as radiation source, a PbSe photoresistor as infrared detector and a programmable interrupt controller (PIC) microcontroller as control unit. The detector system presents a thermoresistor and a thermoelectric cooling to control the detector temperature and keep the noise at low levels. The microcontroller incorporated total autonomy on the proposed photometer. As its components are inexpensive and of easy acquisition, the proposed NIR LED-photometer is an economical alternative for chemical analyses in small routine, research and/or teaching laboratories. By being portable and microcontrolled, it also allows carrying out field chemical analyses. The instrument was successfully applied on the screening analysis to verify adulteration in gasoline samples. 相似文献
99.
Determination of tetracyclines residues in honey by on-line solid-phase extraction high-performance liquid chromatography 总被引:3,自引:0,他引:3
An automated system using on-line solid-phase extraction (SPE) high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection was developed for the determination of tetracyclines (TCs), such as tetracycline (TC), oxytetracycline (OTC), chlortetracycline (CTC), metacycline (MC), and doxycycline (DC) in honey. One milliliter diluted honey sample was injected into a conditioned C18 SPE column and the matrix was washed out with water for 3 min. By rotation of the switching valve, TCs were eluted and transferred to the analytical column by the chromatographic mobile phase. Chromatographic conditions were optimized. TCs were separated in less than 8 min with a gradient elution using a mixture of 0.8% formic acid and acetonitrile. The UV detection was performed at 365 nm. The conditions for on-line SPE, including solvent and total time for loading sample and washing matrix were also optimized. Time for extraction and separation decreased greatly. For the five kinds of TCs, the limits of detection (LODs) at a signal-to-noise of 3 ranged from 5 to 12 ng g−1. The relative standard deviations (R.S.D.) for the determination of TCs ranged from 3.4 to 7.1% within a day and ranged from 3.2 to 8.9% in 3 days, respectively. 相似文献
100.
An on-line method was developed for the extraction, derivatization and determination of formaldehyde in textile samples. Formaldehyde was first extracted with water by ultrasound assisted, and directly introduced into a derivatization column which was packed with a moderately sulfonated cation-exchange resin. The resin used as solid support for the derivatization was charged with 2,4-dinitrophenylhydrazine (DNPH) previously. The formaldehyde DNPH derivative was eluted with the chromatographic mobile phase into an analytical column for the separation, and then monitored by UV detector. The maximum extraction yield was achieved when the extraction vessel was located at 10mm from the ultrasonic source and 10mg textile sample was extracted with 5mL pure water at a flow rate of 1.0mLmin(-1) at 50 degrees C. The detection limit of the proposed method was 0.06mgkg(-1). This method was applied to the determination of formaldehyde in different textile samples, and compared with the state standard method (off-line spectrophotometry) used in China. The similar contents of formaldehyde were obtained for most samples by the two methods, but little higher for some samples obtained by the proposed method. The average relative standard deviation (RSD) obtained by the on-line method was 3.2% which is lower than 29.5% obtained by the standard method. 相似文献