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11.
细菌纤维素(BC)因其独特性能被广泛应用于医药、食品等领域,目前其高产量菌株筛选、合成成本降低及合成途径改良等成为研究热点。本文依据国内外文献并结合团队研究成果对BC合成与鉴定的相关研究进行综述。首先对BC合成菌筛选及碳源利用的研究进行了分析,总结了降低BC合成成本的研究思路。其次对鉴定菌株合成产物的方法进行了归纳,总结了不同方法的特点。然后结合本团队筛选出的BC生产菌XJL-06-4 BC合成酶基因分析结果,综述了BC合成途径、合成酶存在形式以及基因水平调控作用,为BC在分子水平上通过改变合成途径提高产量提供新思路。最后,总结BC微生物发酵生产存在的问题,多角度提出解决方案。  相似文献   
12.
采用乙二胺基乙磺酸钠(AAS)作为亲水剂,在二月桂酸二丁基锡(DBTDL)的催化下,通过异佛尔酮二异氰酸酯(IPDI)将亲水基引入二醋酸纤维(CA)分子中,制得了一种氨基磺酸盐型水性醋酸纤维乳液(SWCA)。利用FTIR、DLS、黏度计、TEM、SEM、接触角测量仪、XRD、TGA,对SWCA结构及涂膜性能进行表征。考察了IPDI与AAS物质的量比对SWCA乳液粒径、黏度、涂膜表观形貌及耐水性的影响。结果表明:当n(IPDI)∶n(AAS)=1.1∶1时,乳液最稳定,微观形态呈水包油型(O/W)核壳结构,乳液粒径和分散系数(PDI)最小,分别为128nm和0.112,此时乳液表观黏度最大,为73.5m Pa·s,所成涂膜致密平整,接触角可达110.2°±2°,表现出明显的疏水性;此外,与二醋酸纤维相比,SWCA涂膜结晶性减弱,呈微晶态或次晶态结构,且具有较好的耐热性。  相似文献   
13.
Reinforcement of PEEK by nanoparticles such as multiwalled carbon nanotubes (MWCNTs), is a promising technique to prepare PEEK nanocomposites with improved properties for promising biomedical applications. However, proper dispersion of MWCNTs in the polymer matrices is a primary processing challenge. The present study reports a novel and environmentally beneficial approach for homogeneous dispersion of MWCNT in PEEK by using ionic liquid (IL) 1-ethyl-3-methylimidazolium hydrogen sulfate ([EMIM][HSO4]). Neat PEEK, PEEK-MWCNTs (using conventional organic solvent dimethylformamide), and PEEK-MWCNTs-IL (using [EMIM][HSO4]) nanocomposites were fabricated via melt-compounding and compression molding techniques. The fabricated composites were characterized for morphological, thermal, and mechanical properties and compared to those of neat PEEK and PEEK-MWCNTs. Ionic liquid provoked proficient dispersion of the MWCNTs in PEEK, as confirmed by FESEM and optical micrographs. The thermal stability of PEEK-MWCNTs-IL composite was significantly superior to that of the neat PEEK and PEEK-MWCNTs. Analysis of tensile strength and nanoindentation depicted that the modulus of elasticity of PEEK-MWNCTs-IL was significantly increased by 76% as compared to that of neat PEEK. We believe that the present work could provide a new and green platform for the manufacturing of PEEK nanocomposites with enhanced dispersion of nanofillers for biomedical applications.  相似文献   
14.
There is currently considerable interest in developing stiff, strong, tough, and heat resistant poly(lactide) (PLA) based materials with improved melt elasticity in response to the increasing demand for sustainable plastics. However, simultaneous optimization of stiffness, strength, and toughness is a challenge for any material, and commercial PLA is well-known to be inherently brittle and temperature-sensitive and to show poor melt elasticity. In this study, we report that high-shear mixing with cellulose nanocrystals (CNC) leads to significant improvements in the toughness, heat resistance, and melt elasticity of PLA while further enhancing its already outstanding room temperature stiffness and strength. This is evidenced by (i) one-fold increase in the elastic modulus (6.48 GPa), (ii) 43% increase in the tensile strength (87.1 MPa), (iii) one-fold increase in the strain at break (∼6%), (iv) two-fold increase in the impact strength (44.2 kJ/m2), (v) 113-fold increase in the storage modulus at 90°C (787.8 MPa), and (vi) 103-fold increase in the melt elasticity at 190°C and 1 rad/s (∼105 Pa) via the addition of 30 wt% CNC. It is hence possible to produce industrially viable, stiff, strong, tough, and heat resistant green materials with improved melt elasticity through high-shear mixing.  相似文献   
15.
A novel process for the production of superabsorbent materials (hydrogels) from bacterial cellulose (BC) was developed. Prior to crosslinking with a water‐soluble polyethylene glycol diacrylate (PEGDA), BC was first carboxymethylated and functionalized with glycidyl methacrylate. The degree of crosslinking influenced the swelling properties of the hydrogels. The use of greater amounts of PEGDA enhanced the formation of a thicker macromolecular network containing fewer capillary spaces in the crosslinked gel. The maximum water retention value of the hydrogels containing 2.5–3.5 mmol of carboxyl groups per gram of gel reached 125 g g?1 in distilled water, and 29 g g?1 in saline (0.9% NaCl solution). The highly porous hydrogel architecture with a pore size of 350–600 µm created a high specific surface area. This enables rapid mass penetration in superabsorbent applications. The superabsorbent hydrogels reached 80% of their maximum water absorption capacity in 30 min. © 2018 Society of Chemical Industry  相似文献   
16.
Cellulose dissolved in ionic liquid (1‐(carboxymethyl)pyridinium chloride)/water (60/40 w/w) mixture is regenerated in various non‐solvents, namely water, ethanol, methanol and acetone, to gain more insight into the contribution of non‐solvent medium to the morphology of regenerated cellulose. To this end, the initial and regenerated celluloses were characterized with respect to crystallinity, thermal stability, chemical structure and surface morphology using wide‐angle X‐ray diffraction, thermogravimetric analysis, Fourier transform infrared spectroscopy and scanning electron microscopy. According to the results, regardless of non‐solvent type, all regenerated samples have the same chemical structure and lower crystallinity in comparison to the initial cellulose, making them a promising candidate for efficient biofuel production based on enzymatic hydrolysis of cellulose. The reduction in crystallinity of regenerated samples is explained based on the potential of the non‐solvent to break the hydrogen bonds between cellulose chains and ionic liquid molecules as well as the affinity of water and non‐solvent which can be evaluated based on Hansen solubility parameter. The latter also determines the phase‐separation mechanism during the regeneration process, which in turn affects surface morphology of the regenerated cellulose. The pivotal effect of regenerated cellulose crystallinity on its thermal stability is also demonstrated. Regenerated cellulose with lower crystallinity is more susceptible to molecular rearrangement during heating and hence exhibits enhanced thermal stability. © 2019 Society of Chemical Industry  相似文献   
17.
The issues related to renewable energy sources is a matter of great worldwide appeal due to the increasing energy demand, instability in oil prices and environmental problems. In this context, the purpose of this study was to prepare self-assembled films of polyallylamine hydrochloride and poly (acrylic acid) supported onto bacterial cellulose membranes by a layer-by-layer approach with titanium dioxide (TiO2) nanoparticles and different concentrations of gold for application in hydrogen gas (H2) production by photocatalysis. The influence of the gold concentration and the presence and size of the gold nanoparticles (Au NPs), as well as the surface and thickness of the films on H2 production was investigated. The results showed that the film, prepared with a lower concentration of gold, presented the smallest Au NPs and, therefore, greater contact with the TiO2 nanoparticle surfaces, producing more H2. By analyzing the variation in all the experimental parameters used in the preparation of the films, it can be concluded that the best H2 production achieved was 29.12 μmol h?1 cm2.  相似文献   
18.
陆佳  刘伟  王欣  苏小红  范超 《化工进展》2020,39(9):3635-3642
以玉米秸秆为原料,通过碳化-磺化法制备了碳基固体酸(CSA),采用XRD、FTIR、XPS、SEM、阳离子交换与返滴定法等手段对其结构形貌进行表征,并考察了制备条件对固体酸表面活性基团含量与催化活性的影响。以NaOH/尿素冻融预处理后的纤维素为底物,研究了CSA催化纤维素水解糖化的效果与条件。结果表明:NaOH/尿素冻融预处理能够有效辅助固体酸催化纤维素水解,在350℃碳化2h、100℃磺化5h条件下制备的CSA催化性能最好,其酸量达3.94mmol/g,其中磺酸基、羧基、酚羟基含量分别为1.09mmol/g、1.36mmol/g、1.49mmol/g。在m(CSA)∶m(纤维素)=3∶1、水解温度200℃、水解时间为0.5h的条件下,纤维素水解还原糖得率与转化率分别为47.1%和63%。CSA循环利用3次催化活性下降不大。本研究可为废弃生物质原料制备的固体酸催化纤维素水解转化利用提供科学参考。  相似文献   
19.
In the present work blends of polystyrene (PS) with sepiolites have been produced using a melt extrusion process. The dispersion degree of the sepiolites in the PS has been analyzed by dynamic shear rheology and X-ray micro-computed tomography. Sepiolites treated with quaternary ammonium salts (O-QASEP) are better dispersed in the PS matrix than natural sepiolites (N-SEP) or sepiolites organo-modified with silane groups (O-SGSEP). A percolated network is obtained when using 6.0 wt% of O-QASEP, 8.0 wt% of N-SEP and 10.0 wt% of O-SGSEP. It has been shown that multiple extrusion processes have a negative effect on the polymer architecture. They produce a reduction in the length of the polymeric chains, and they do not lead to a better dispersion of the particles in the polymer matrix. Foams have been produced using a gas dissolution foaming process, where a strong effect of the dispersion degree on the cellular structure of the different foams was found. The effects on the cellular structure obtained by using different types of sepiolites, different contents of sepiolites and different extrusion conditions have been analyzed. The foams produced with the formulations containing O-QASEP present the lowest cell size and the most homogeneous cellular structures.  相似文献   
20.
Contamination of water resources by toxic heavy metals has significant impacts on environmental and human health. Their removal from aqueous media is essential to ensure water sustainability and to provide safe freshwater availability to population. Electrospun chitosan (CS) nonwoven mats are efficient at removing heavy metals from aqueous media. However, they suffer from low permeability and low-mechanical strength. They are also unable to remove contaminants in a nonselective way. A bilayer sorbent media made of a porous phosphorylated cellulose substrate covered by electrospun CS nanofibers was developed to overcome those weaknesses. The hydrophilic composite shows good water permeability and mechanical strength with appropriate thermal and chemical characteristics. Adsorption tests with Cd(II) indicate that pseudo-second order and Langmuir models best fitted experimental data, with a maximum adsorption capacity of 591 mg/g at 25°C. Adsorption with multielement samples containing Cr(VI), Cu(II), Cd(II), and Pb(II) also reveal their capability to remove them in a selective way. This mechanically resistant, hydrophilic, and permeable adsorbent media was able to capture both cationic and anionic metallic contaminants.  相似文献   
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