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21.
22.
Protein encapsulation is a growing area of interest, particularly in the fields of food science and medicine. The sequestration of protein cargoes is achieved using a variety of methods, each with benefits and drawbacks. One of the most significant challenges associated with protein encapsulation is achieving high loading while maintaining protein viability. This difficulty is exacerbated because many encapsulant systems require the use of organic solvents. By contrast, nature has optimized strategies to compartmentalize and protect proteins inside the cell—a purely aqueous environment. Although the mechanisms whereby aspects of the cytosol is able to stabilize proteins are unknown, the crowded nature of many newly discovered, liquid phase separated “membraneless organelles” that achieve protein compartmentalization suggests that the material environment surrounding the protein may be critical in determining stability. Here, encapsulation strategies based on liquid–liquid phase separation, and complex coacervation in particular, which has many of the key features of the cytoplasm as a material, are reviewed. The literature on protein encapsulation via coacervation is also reviewed and the parameters relevant to creating protein‐containing coacervate formulations are discussed. Additionally, potential opportunities associated with the creation of tailored materials to better facilitate protein encapsulation and stabilization are highlighted. 相似文献
23.
Mani Balamurugan Hui‐Yun Jeong Venkata Surya Kumar Choutipalli Jung Sug Hong Hongmin Seo Natarajan Saravanan Jun Ho Jang Kang‐Gyu Lee Yoon Ho Lee Sang Won Im Venkatesan Subramanian Sun Hee Kim Ki Tae Nam 《Small (Weinheim an der Bergstrasse, Germany)》2020,16(25)
The electrochemical reduction of carbon dioxide (CO2) to hydrocarbons is a challenging task because of the issues in controlling the efficiency and selectivity of the products. Among the various transition metals, copper has attracted attention as it yields more reduced and C2 products even while using mononuclear copper center as catalysts. In addition, it is found that reversible formation of copper nanoparticle acts as the real catalytically active site for the conversion of CO2 to reduced products. Here, it is demonstrated that the dinuclear molecular copper complex immobilized over graphitized mesoporous carbon can act as catalysts for the conversion of CO2 to hydrocarbons (methane and ethylene) up to 60%. Interestingly, high selectivity toward C2 product (40% faradaic efficiency) is achieved by a molecular complex based hybrid material from CO2 in 0.1 m KCl. In addition, the role of local pH, porous structure, and carbon support in limiting the mass transport to achieve the highly reduced products is demonstrated. Although the spectroscopic analysis of the catalysts exhibits molecular nature of the complex after 2 h bulk electrolysis, morphological study reveals that the newly generated copper cluster is the real active site during the catalytic reactions. 相似文献
24.
Irina Terekhova Iliya Kritskiy Mikhail Agafonov Roman Kumeev Carlos Martínez-Corts Horacio Prez-Snchez 《International journal of molecular sciences》2020,21(23)
The selectivity of encapsulation of leflunomide and teriflunomide by native α-, β- and γ-cyclodextrins was investigated through 1H NMR and molecular modeling. Thermodynamic analysis revealed the main driving forces involved in the binding. For α-cyclodextrin, the partial encapsulation was obtained while deep penetration was characterized for the other two cyclodextrins, where the remaining polar fragment of the molecule is located outside the macrocyclic cavity. The interactions via hydrogen bonding are responsible for high negative enthalpy and entropy changes accompanying the complexation of cyclodextrins with teriflunomide. These results were in agreement with the molecular modeling calculations, which provide a clearer picture of the involved interactions at the atomic level. 相似文献
25.
Purushottam B. Tiwari Prem P. Chapagain Ahmed Seddek Thirunavukkarasu Annamalai Aykut Üren Yuk-Ching Tse-Dinh 《ChemMedChem》2020,15(7):623-631
A topoisomerase-DNA transient covalent complex can be a druggable target for novel topoisomerase poison inhibitors that represent a new class of antibacterial or anticancer drugs. Herein, we have investigated molecular features of the functionally important Escherichia coli topoisomerase I (EctopoI)-DNA covalent complex (EctopoIcc) for molecular simulations, which is very useful in the development of new antibacterial drugs. To demonstrate the usefulness of our approach, we used a model small molecule (SM), NSC76027, obtained from virtual screening. We examined the direct binding of NSC76027 to EctopoI as well as inhibition of EctopoI relaxation activity of this SM via experimental techniques. We then performed molecular dynamics (MD) simulations to investigate the dynamics and stability of EctopoIcc and EctopoI-NSC76027-DNA ternary complex. Our simulation results show that NSC76027 forms a stable ternary complex with EctopoIcc. EctopoI investigated here also serves as a model system for investigating a complex of topoisomerase and DNA in which DNA is covalently attached to the protein. 相似文献
26.
An effective electron-injection layer (EIL) is crucial to the development of highly efficient polymer light-emitting diodes (PLEDs) using stable, high work-function aluminium as the cathode. This work presents the first investigation using hydroxyethyl cellulose (HEC), filled with chelate complexes [(CH3COO)2-M, EDTA-M; M: Ca2+, Mg2+], as an electron-injection layer (EIL) to fabricate multilayer polymer light-emitting diodes (ITO/PEDO:PSS/HY-PPV/EIL/Al) by spin-coating processes. Devices based on HEC doped with EDTA-M provided the best performance. The maximum luminance and maximum current efficiency of polymer light-emitting diodes with EDTA-Ca in an HEC layer were 7502 cd/m2 and 2.85 cd/A, respectively, whereas those with EDTA-Mg were 8443 cd/m2 and 3.12 cd/A, which was approximately seven- to eight-fold of that without EIL. This performance enhancement was attributed to electron donation from the chelator that reduces metal cations to a “pseudo-metallic state”, enabling it to act as an intermediate step to facilitate electron injection. The results demonstrate that chelates of bivalent cations with EDTA can potentially serve as electron-injection materials for optoelectronic applications. 相似文献
27.
Chenjie Wang Yanting Chen Yanru Cui Tianqi Zhang Dongliang Zhang Chengye Ma Shanfeng Chen Hongjun Li 《International Journal of Food Science & Technology》2021,56(9):4780-4788
Camellia oil (CO) microcapsules were developed using chitosan–soybean protein isolate (CS-SPI) complexes as wall materials and transglutaminase (TGase) as the cross-linking agent. Results indicated that CO/SPI under the ratio of 1:2 exhibited the highest microencapsulation efficiency and yield, possessing the best encapsulation effect. Morphology observation showed that CO microcapsules were intact, compact and nearly spherical. The microencapsulated CO exhibited the improved thermal resistance and significantly lower peroxide values after 3 days storage, demonstrating that the produced microcapsule was a promising way to maintain the thermal and oxidative stability of camellia oil. It could be found evidence from FTIR, which indicated that covalent cross-linking and hydrogen bonding might be involved among wall materials, and physical interactions between the core and wall materials. Therefore, the produced CO microcapsules could be an effective way to protect camellia oil, which was helpful for improving the processing and storage qualities of camellia oil. 相似文献
28.
Conventional thermally activated delayed fluorescence (TADF) molecules achieve small energy differences between the lowest singlet and triplet excited states (ΔEST) by enhancing the intramolecular charge transfer, which inevitably leads to a wide emission spectrum and low fluorescence rate. Here, we prepared a deep blue TADF molecule via a small ΔEST pyridine-phenol fluoroboron complex as the acceptor. The small ΔEST is maintained when carbazole donors are attached to the 4-position of the phenyl rings in the fluoroboron complex. Benefiting from the strong electron coupling between the donor (D) and acceptor (A) moieties, the compound Cz-4-BF exhibits a high fluorescence rate of 4.8 × 108 s−1 and a small D-A dihedral angle change in the excited state. Consequently, a photoluminescence (PL) quantum yield of nearly 100% and a PL spectrum with full-width at half-maximum (FWHM) < 60 nm were obtained in solution and low-concentration doped films. A TADF-sensitized fluorescence (TSF) device containing Cz-4-BF achieves an external quantum efficiency of 21%, which is higher than the devices employing classical fluorescent emitters and multiple resonance-type TADF emitters. The Cz-4-BF-based TSF device shows significantly improved color coordinates of (0.14, 0.10) versus a control device without Cz-4-BF. 相似文献
29.
This article proposes a complex network methodology for the process of Environmental Impact Assessment (EIA) that limits subjectivity and reduces uncertainty by incorporating elements of complex systems theory in the stages of identification and assessment of the significance of environmental impacts. The proposed methodology reduces the sources of uncertainty, which emerge from the use of simplified models that analyse the environment-activity interactions in a unidirectional fashion. This proposal determines the significance of environmental impacts through multidirectional or complex causal relationships. Likewise, it limits the subjectivity of the evaluator by using these causality relationships instead of criteria based on the impacts’ attributes. The application of the proposed methodology demonstrates the advantages of (i) prioritizing the impacts according to their capacity to interact with other impacts, and (ii) the possibility to redirect the environmental management plans towards the prevention of impacts of higher complexity and to reduce the importance of derived impacts.
The application of the proposed methodology reveals that the percentage of irrelevant and moderate impacts is reduced, whereas the percentage of severe and critical impacts increase, in comparison to the conventional methodologies. 相似文献
30.
为实现亮度不均的复杂纹理背景下表面划痕的鲁棒、精确、实时识别,提出一种基于深度神经网络的表面划痕识别方法。用于表面划痕识别的深度神经网络由风格迁移网络和聚焦卷积神经网络(CNN)构成,其中风格迁移网络针对亮度不均的复杂背景下的表面划痕进行预处理,风格迁移网络包括前馈转换网络和损失网络,首先通过损失网络提取亮度均匀模板的风格特征和检测图像的知觉特征,对前馈转换网络进行离线训练,获取网络最优参数值,最终使风格迁移网络生成亮度均匀且风格一致的图像,然后,利用所提出的基于聚焦结构的聚焦卷积神经网络对生成图像中的划痕特征进行提取并识别。以光照变化的金属表面为例,进行划痕识别实验,实验结果表明:与需要人工设计特征的传统图像处理方法及传统深度卷积神经网络相比,划痕漏报率低至8.54%,并且收敛速度更快,收敛曲线更加平滑,在不同的深度模型下均可取得较好的检测效果,准确率提升2%左右。风格迁移网络能够保留完整划痕特征的同时有效解决亮度不均的问题,从而提高划痕识别精度;同时聚焦卷积神经网络能够实现对划痕的鲁棒、精确、实时识别,大幅度降低划痕漏报率和误报率。 相似文献