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991.
Lei Zhang Wei Zhang Nianchen Zhou Jian Zhu Zhengbiao Zhang Zhenping Cheng 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(9):876-885
One linear and two miktoarm star side-chain liquid crystalline (LC) block copolymers with p-methoxyazobenzene moieties were prepared by a combination of ring-opening polymerization (ROP) and atom transfer radical polymerization (ATRP) techniques. First, ROPs of ε -caprolactone (ε -CL) were carried out catalyzed by Sn(Oct)2 using three multifunctional initiators, hydroxyethyl 2-bromoisobutyrate (AB type), 3-hydroxy-2-(hydroxymethyl)-2-methylpropyl 2-bromo-2-methylpropanoate (A2B type) and 2,2-bis(hydroxymethyl)propane-1,3-diyl bis(2-bromo-2-methylpropanoate) (A2B2 type), at 110°C in toluene, respectively. Second, the previously obtained poly(ε -caprolactone)s (PCLs) with bromines functionalities were used as the macroinitiators to conduct ATRP of 6-(4-methoxy-4-oxy-azobenzene) hexyl methacrylate (MMAZO) with CuBr/PMDETA as the catalyst systems at 85°C in anisole to prepare the linear and miktoarm side-chain LC block copolymers (PCL-b-PMMAZO, (PCL)2-(PMMAZO) and (PCL)2-(PMMAZO)2). The produced polymers were well-controlled with the controlled molecular weights and the relatively narrow molecular weight distributions (M w/M n ≤ 1.35). The structures of the obtained polymers were all characterized by NMR, FT-IR and GPC analysis. Furthermore, the LC properties of the linear and miktoarm star block copolymers were also investigated by differential scanning calorimetry (DSC) and thermal polarized optical microscopy (POM). 相似文献
992.
In this paper, the diffusion mechanism of as‐spun PAN fiber was investigated in dimethyl sulfoxide‐water by determining the dynamic compositions of the fibers and the diffusion coefficients of solvent and nonsolvent during coagulation. The diffusion process could be divided into two stages. Results showed that the first stage of the diffusion process was the most important during the whole process, which was fundamental to further study on the formation mechanism. Also, compared with wet spinning, the dry‐jet wet spinning method had the advantage of mild coagulating at a high jet‐stretch. At high concentrations, the diffusion coefficients increased and the ratio of solvent diffusion coefficient to nonsolvent diffusion coefficient decreased; an increasing temperature resulted in the increase of both diffusion coefficients with a decrease in their ratios. To some extent, for the PAN‐DMSO‐water system, the more the ratios Ds*/Dn* tended to 1, the more the cross‐section shapes of as‐spun PAN fiber tended to be circular. 相似文献
993.
A water-soluble monomer N1-(4-vinylbenzyl)-pentane-1,5-diamine dihydrochloride (VBPDA) with cadaverine (1,5-pentanediamine) group was synthesized. pH-responsive polymer with cadaverine group was obtained by free radical polymerization of VBPDA using 4,4-azobis(4-cyanovaleric acid) (ACVA) as the initiator. The structure and molecular weight of the polymer were characterized by FTIR, 1H-NMR and GPC-MALLS. Aggregation behavior of the polymer in aqueous solution was investigated by dynamic light scattering (DLS), UV-Vis and fluorescence measurements. The experimental results show that the fluorescence intensity of the aggregates decreases and the size of the aggregates increases with increasing pH due to the continuous dehydration of the cadaverine side groups. 相似文献
994.
Ming Zeng Huina Gao Yaoqing Wu Liren Fan Tihe Zheng Dongfang Zhou 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(10):1042-1049
In order to prepare the advanced cellulosic super-absorbent polymer with high grafting level, we tried the novel ultrasound wave assisting polyethylene glycol (PEG) pre-treatment method to decrease the crystallinity and increase the accessibility of cellulose fiber. The effects of ultrasonification assisting PEG method on the crystallinity and swelling capacity of cellulose fiber were investigated. To optimize the experimental condition, the Taguchi method was employed in the treatment process. The influence factors such as ultrasonic wave power, ultrasonic wave time and PEG molecular weight relative to the crystallinity of cellulose fiber were studied systematically. The degree of crystallinity of cellulose fiber was measured by wide-angle X-ray diffraction (WAXD). The morphology of cellulose fiber was observed by environment scanning electron microscopy (ESEM). The effects of pre-treatment variables on the water absorbency and water retention values of cellulose fiber were also investigated. The research results revealed that, under the optimal experimental condition (ultrasonic powder, 500 W; ultrasonic time, 150 s; PEG molecular weight, 600 g/mol), the crystallinity of cellulose fiber decreased from 72.16 to 42.95%. Accordingly, the absorbency of cellulose fiber increased from 1.436 to 2.063 g/g, and the water retention value increased from 47.21 to 113.4%. However, the morphology of cellulose fiber did not change thoroughly compared with the original cellulose fiber. It can be hypothesized that the original inter- and intra-macromolecular hydrogen bonds in cellulose network were weakened, resulting from the high level dispersion of PEG within cellulose network without breaking the surface morphology of fiber. 相似文献
995.
Chao Luo Qianxiong Zhou Wanhua Lei Jianguang Wang Baowen Zhang 《Supramolecular chemistry》2013,25(9):657-662
A new unsymmetrical aniline-based squaraine (SQ2) bearing binding unit of Hg2+ ion was designed and synthesised. SQ2 can form 1:2 inclusion complex with β-cyclodextrin, and the resulting complex, which undergoes absorption and fluorescence bleaching upon binding Hg2+, can serve as a turn-on colorimetric or fluorescent chemosensor in organic solvent-free aqueous solution for thiol-containing amino acids with high selectivity and tunable measuring range. 相似文献
996.
We provide a highly sensitive and selective assay to detect Hg2+ in aqueous solutions using a novel β-functionalised porphyrin-based chemosensor 5 at room temperature. The binding properties of the chemosensor 5 for cations were examined by UV–vis spectroscopy and 1H NMR. The results indicate that a 1:1 stoichiometric complex is formed between chemosensor 5 and mercury (II) ion. The recognition mechanism between chemosensor 5 and metal ion was discussed based on their absorbance changes and the chemical shift changes when they interact with each other. Control experiments revealed that chemosensor 5 has a selective response to mercury (II) ion compared with other metal ions. 相似文献
997.
998.
Highlights? The complete gougerotin biosynthetic gene cluster is cloned ? Heterologous production of gougerotin is accomplished in S. coelicolor M1146 ? Biosynthetic pathway is proposed based on bioinformatics, genetic, and chemical analyses ? Preliminary data support an uncommon enzymatic reaction for peptide bond formation 相似文献
999.
Functionalized multiwall carbon nanotubes (f-MWCNTs) with varying functionalization degrees were prepared by chemical methods. The effect of f-MWCNTs on the cure kinetics of bismaleimide–triazine (BT) resin was studied through nonisothermal differential scanning calorimetry (DSC) methods. The reaction activation energy (E α ) was determined by Flynn–Wall–Ozawa method. The results show that f-MWCNTs have more acceleration ability than pristine MWCNTs, due to more groups on the surface of f-MWCNTs than that of pristine MWCNTs. The activation energy was decreased from a value of 91.3 kJ mol?1 for the neat BT resin to 74.2 kJ mol?1 at the small mass loading (1.0 %) of f7-MWCNTs. The effect of f-MWCNTs on the reaction mechanism has been investigated. It shows that the f-MWCNTs accelerate the cure reaction of BT resin by providing the Lewis acids (H+) to make the “Diels–Alder” reaction and “ENE” reaction of BT resins more efficient. These findings offer useful insights into the cure technology of thermosetting resin filled with f-MWCNTs, without negative effect on the cure reaction. 相似文献
1000.
Yu Mo Lei Zhao Chia-Lung Chen Giin Yu Amy Tan Jing-Yuan Wang 《Journal of Thermal Analysis and Calorimetry》2013,111(1):781-788
Pyrolysis is one important way to treat polystyrene waste and upcycle it into useful materials. A comparative pyrolysis study of virgin polystyrene (VPS) and two types of commonly used polystyrene products, expanded polystyrene (EPS) and polystyrene container (CPS) was carried out. Various values were found in the thermodynamic study and kinetic study of VPS, EPS, and CPS pyrolysis, suggesting distinct thermal degradation characteristics of these materials. The energy barrier order of the pyrolysis processes was EPS, CPS, VPS, showing activation energy of 230, 219, and 145 kJ mol?1, respectively. The order of amount of heat absorbed was EPS, CPS, VPS, with enthalpy of 224, 213, and 139 kJ mol?1, respectively. The reaction favorability order was EPS, CPS, and VPS with Gibbs free energy of 118, 132, and 210 kJ mol?1, respectively. Thermogravimetric analysis indicated the use of high heating rate would increase the reaction rate and shorten the reaction time. Product evolution profiles showed that VPS and CPS pyrolysis produced mainly aromatics, while EPS pyrolysis produced aromatics at the initial phase of the reaction and aliphatic hydrocarbon at the latter phase. The diverse pyrolysis behaviors of VPS, EPS, and CPS demonstrated that an examination on different polystyrene materials was desired to optimize the pyrolysis conditions and product distribution, and thus benefit the process of valuable materials recovery. 相似文献