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排序方式: 共有493条查询结果,搜索用时 15 毫秒
1.
Dealloyed nanoporous gold (np-Au) has applications as oxygen reduction catalysis in Li-air batteries and fuel cells, or as actuators to convert electricity into mechanical energy. However, it faces the challenges of coarsening-induced structure instability, mechanical weakness due to low relative densities, and slow dealloying rates. Here, monolithic np-Au is dealloyed from a single-phase Au25Ni75 solid-solution at a one-order faster dealloying rate, ultra-low residual Ni content, and importantly, one-third more relative density than np-Au dealloyed from conventional Au25Ag75. The small atomic radius and low dealloying potential of the sacrificing element Ni are intrinsically beneficial to fast produce high relative density np-Au, as predicted by a general model for dealloying of binary alloys and validated by experiments. Stable, durable, and reversible actuation of np-Au takes place under cyclic potential triggering in alkaline and acidic electrolytes with negligible coarsening-induced strain-shift. The thermal and mechanical robustness of bulk np-Au is confirmed by two-order slower ligament coarsening rates during annealing at 300 °C and 45 MPa macroscopic yielding strength distinctive from the typical early onset of plastic yielding. This article opens a rich direction to achieve high relative density np-Au which is essential for porous network connectivity, mechanical strength, and nanostructure robustness for electrochemical functionality. 相似文献
2.
Alec T. Salminen Jingkai Zhang Gregory R. Madejski Tejas S. Khire Richard E. Waugh James L. McGrath Thomas R. Gaborski 《Small (Weinheim an der Bergstrasse, Germany)》2019,15(6)
Selective cellular transmigration across the microvascular endothelium regulates innate and adaptive immune responses, stem cell localization, and cancer cell metastasis. Integration of traditional microporous membranes into microfluidic vascular models permits the rapid assay of transmigration events but suffers from poor reproduction of the cell permeable basement membrane. Current microporous membranes in these systems have large nonporous regions between micropores that inhibit cell communication and nutrient exchange on the basolateral surface reducing their physiological relevance. Here, the use of 100 nm thick continuously nanoporous silicon nitride membranes as a base substrate for lithographic fabrication of 3 µm pores is presented, resulting in a highly porous (≈30%), dual‐scale nano‐ and microporous membrane for use in an improved vascular transmigration model. Ultrathin membranes are patterned using a precision laser writer for cost‐effective, rapid micropore design iterations. The optically transparent dual‐scale membranes enable complete observation of leukocyte egress across a variety of pore densities. A maximal density of ≈14 micropores per cell is discovered beyond which cell–substrate interactions are compromised giving rise to endothelial cell losses under flow. Addition of a subluminal extracellular matrix rescues cell adhesion, allowing for the creation of shear‐primed endothelial barrier models on nearly 30% continuously porous substrates. 相似文献
3.
4.
Haixia Qian Xiaobo Mu Kaiyang Li Shenghui Xie Xinbo Xiong Xierong Zeng 《Materials Science & Technology》2020,36(10):1083-1091
ABSTRACT Nanoporous copper (NPC) with a controllable ligament width was prepared by chemically dealloying Cu45Al45Ti10 amorphous ribbons in dilute HCl solution. X-ray diffraction and scanning electron microscopy analysis confirmed the 3D, bicontinuous, nanoporous structure constituting fcc-Cu ligaments of 39–79?nm thickness. The coarsening of NPC ligaments increased significantly with an increase of HCl concentration, reaction temperature or time. The surface diffusivity and activation energy of NPC were also calculated. Finally, the catalytic activity of NPC was validated with the ultrasound and H2O2-assisted degradation of methyl orange (MO), where 99% MO was degraded within 15?min. 相似文献
5.
Formation of capillary vessel structures in scaffolds is critical for engineering various tissues and organs. Various biofabrication techniques are developed in recent years to create scaffolds integrated with perfusion channels. However, rapid fabrication of artificial capillary vessels (<10 µm) still remains challenging. In this study, a novel electrospinning approach is developed to fabricate nanoporous polycaprolactone microtubes as potential functional capillaries. The results show that ambient environment parameters and solution properties affect the pore formation and tube morphology. Porous microbeads, helical fibers, and microtubes were fabricated under different processing conditions. The optimal tubular structure is obtained with consistent viscosities between the core and the sheath solutions. The biomimetic nanoporous microtubes hold great potential for vascularization in tissue engineering. 相似文献
6.
Rui-Qi Yao Yi-Tong Zhou Hang Shi Wu-Bin Wan Qing-Hua Zhang Lin Gu Yong-Fu Zhu Zi Wen Xing-You Lang Qing Jiang 《Advanced functional materials》2021,31(10):2009613
Electrocatalytic hydrogen evolution in alkaline and neutral media offers the possibility of adopting platinum-free electrocatalysts for large-scale electrochemical production of pure hydrogen fuel, but most state-of-the-art electrocatalytic materials based on nonprecious transition metals operate at high overpotentials. Here, a monolithic nanoporous multielemental CuAlNiMoFe electrode with electroactive high-entropy CuNiMoFe surface is reported to hold great promise as cost-effective electrocatalyst for hydrogen evolution reaction (HER) in alkaline and neutral media. By virtue of a surface high-entropy alloy composed of dissimilar Cu, Ni, Mo, and Fe metals offering bifunctional electrocatalytic sites with enhanced kinetics for water dissociation and adsorption/desorption of reactive hydrogen intermediates, and hierarchical nanoporous Cu scaffold facilitating electron transfer/mass transport, the nanoporous CuAlNiMoFe electrode exhibits superior nonacidic HER electrocatalysis. It only takes overpotentials as low as ≈240 and ≈183 mV to reach current densities of ≈1840 and ≈100 mA cm−2 in 1 m KOH and pH 7 buffer electrolytes, respectively; ≈46- and ≈14-fold higher than those of ternary CuAlNi electrode with bimetallic Cu–Ni surface alloy. The outstanding electrocatalytic properties make nonprecious multielemental alloys attractive candidates as high-performance nonacidic HER electrocatalytic electrodes in water electrolysis. 相似文献
7.
Geoffrey Lawrence Arun V Baskar Mohammed H El-Newehy Wang Soo Cha Salem S Al-Deyab Ajayan Vinu 《Science and Technology of Advanced Materials》2015,16(2)
Three-dimensional cage-like mesoporous FDU-12 materials with large tuneable pore sizes ranging from 9.9 to 15.6 nm were prepared by varying the synthesis temperature from 100 to 200 °C for the aging time of just 2 h using a tri-block copolymer F-127(EO106PO70EO106) as the surfactant and 1,3,5-trimethyl benzene as the swelling agent in an acidic condition. The mesoporous structure and textural features of FDU-12-HX (where H denotes the hydrothermal method and X denotes the synthesis temperature) samples were elucidated and probed using x-ray diffraction, N2 adsorption, 29Si magic angle spinning nuclear magnetic resonance, scanning electron microscopy and transmission electron microscopy. It has been demonstrated that the aging time can be significantly reduced from 72 to 2 h without affecting the structural order of the FDU-12 materials with a simple adjustment of the synthesis temperature from 100 to 200 °C. Among the materials prepared, the samples prepared at 200 °C had the highest pore volume and the largest pore diameter. Lysozyme adsorption experiments were conducted over FDU-12 samples prepared at different temperatures in order to understand their biomolecule adsorption capacity, where the FDU-12-HX samples displayed high adsorption performance of 29 μmol g−1 in spite of shortening the actual synthesis time from 72 to 2 h. Further, the influence of surface area, pore volume and pore diameter on the adsorption capacity of FDU-12-HX samples has been investigated and results are discussed in correlation with the textural parameters of the FDU-12-HX and other mesoporous adsorbents including SBA-15, MCM-41, KIT-5, KIT-6 and CMK-3. 相似文献
8.
目的通过正交实验优化不锈钢表面纳米孔制备工艺。方法通过田口实验方法设计正交试验优化工艺。采用含有氯化钠和硫脲的硝酸溶液阳极氧化制备纳米孔,在含有氯化钠、盐酸和硫酸的水溶液中进行扩孔处理。通过扫描电子显微镜、能谱仪对表面处理后的试样表面形貌和元素进行分析,应用软件统计SEM图片孔隙率,并将孔隙率作为响应指标,利用极差分析和方差分析研究阳极氧化工艺和扩孔时间对表面形貌及孔隙率的影响,并优化工艺参数。结果 SEM照片和5个水平的均值表明,硝酸浓度的提高有利于提高孔隙率,较高的硫脲浓度有利于形成均匀有序的纳米孔结构,氯化钠浓度、氧化时间、氧化电压和扩孔时间对表面形貌和孔隙率影响不明显。元素分析表明,纳米孔的材料仍然是不锈钢,而不是金属氧化物。正交实验优化的工艺参数是:硝酸的体积浓度为90 mL/L,硫脲的质量浓度为3.5 g/L,氯化钠的质量浓度为20 g/L,氧化时间为120 s,氧化电压为5.0 V,扩孔时间为50 s。结论通过实验验证,优化后的工艺能够制备出表面较平整、孔隙率较高的纳米孔结构。 相似文献
9.
Saharnaz Ahmadi Maryam Farokhi Parisa Padidar Mojtaba Falahati 《International journal of molecular sciences》2015,16(8):17289-17302
In this study the effect of surface modification of mesoporous silica nanoparticles (MSNs) on its adsorption capacities and protein stability after immobilization of beta-lactoglobulin B (BLG-B) was investigated. For this purpose, non-functionalized (KIT-6) and aminopropyl-functionalized cubic Ia3d mesoporous silica ([n-PrNH2-KIT-6]) nanoparticles were used as nanoporous supports. Aminopropyl-functionalized mesoporous nanoparticles exhibited more potential candidates for BLG-B adsorption and minimum BLG leaching than non-functionalized nanoparticles. It was observed that the amount of adsorbed BLG is dependent on the initial BLG concentration for both KIT-6 and [n-PrNH2-KIT-6] mesoporous nanoparticles. Also larger amounts of BLG-B on KIT-6 was immobilized upon raising the temperature of the medium from 4 to 55 °C while such increase was undetectable in the case of immobilization of BLG-B on the [n-PrNH2-KIT-6]. At temperatures above 55 °C the amounts of adsorbed BLG on both studied nanomaterials decreased significantly. By Differential scanning calorimetry or DSC analysis the heterogeneity of the protein solution and increase in Tm may indicate that immobilization of BLG-B onto the modified KIT-6 results in higher thermal stability compared to unmodified one. The obtained results provide several crucial factors in determining the mechanism(s) of protein adsorption and stability on the nanostructured solid supports and the development of engineered nano-biomaterials for controlled drug-delivery systems and biomimetic interfaces for the immobilization of living cells. 相似文献
10.
Sergei V. Voitekhovich Vladimir Lesnyak Nikolai Gaponik Alexander Eychmüller 《Small (Weinheim an der Bergstrasse, Germany)》2015,11(43):5728-5739
Capping agents play an important role in the colloidal synthesis of nanomaterials because they control the nucleation and growth of particles, as well as their chemical and colloidal stability. During recent years tetrazole derivatives have proven to be advanced capping ligands for the stabilization of semiconductor and metal nanoparticles. Tetrazole‐capped nanoparticles can be prepared by solution‐phase or solventless single precursor approaches using metal derivatives of tetrazoles. The solventless thermolysis of metal tetrazolates can produce both individual semiconductor nanocrystals and nanostructured metal monolithic foams displaying low densities and high surface areas. Alternatively, highly porous nanoparticle 3D assemblies are achieved through the controllable aggregation of tetrazole‐capped particles in solutions. This approach allows for the preparation of non‐ordered hybrid structures consisting of different building blocks, such as mixed semiconductor and metal nanoparticle‐based (aero)gels with tunable compositions. Another unique property of tetrazoles is their complete thermal decomposition, forming only gaseous products, which is employed in the fabrication of organic‐free semiconductor films from tetrazole‐capped nanoparticles. After deposition and subsequent thermal treatment these films exhibit significantly improved electrical transport. The synthetic availability and advances in the functionalization of tetrazoles necessitate further design and study of tetrazole‐capped nanoparticles for various applications. 相似文献