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Intercalated nanocomposites with poly(butylene terephthalate) (PBT) incorporated between the montmorillonite layers were synthesized from dimethyl terephthalate and 1,4-butane diol by using an in situ interlayer polymerization. The PBT nanocomposites were melt-spun at different organoclay contents to produce monofilaments. The samples were characterized by using wide angle X-ray diffraction, electron microscopy, thermal analysis, and tensile testing. The extent of the clay layer in the PBT was confirmed by using X-ray diffraction and electron microscopy, and the clay layer was found to be highly dispersed on a nanometer scale. The addition of only a small amount of organoclay was enough to improve the thermo-mechanical properties of the PBT hybrid fibers. The hybrids were extruded with various draw ratios (DRs) to examine the tensile mechanical property of the fibers. At DR=1, the ultimate tensile strength of the hybrid fibers increased with the addition of clay up to a critical content and then decreased. However, the initial modulus monotonically increased with increasing amount of organoclay in the PBT matrix. When the DR was increased from 1 to 6, for example, the strength and the initial modulus values of the hybrids containing 3 wt% organoclay decreased linearly. 相似文献
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Sridhar Komarneni Bharat L. Newalkar Dongsheng Li Tarun Gheyi Christina L. Lopano Peter J. Heaney Jeffrey E. Post 《Journal of Porous Materials》2003,10(4):243-248
Several nitrate containing anionic clays were synthesized at different temperatures and the kinetics of NO3
– release were determined to test their suitability as slow-release N fertilizers. A sample (Mg:Al = 2:1) synthesized at 60°C with smaller particle size released 75, 86 and 100% of its NO3
– in 1, 3 and 7 days, respectively when equilibrated with a simulated soil solution. On the other hand, the 175°C/2 hrs sample with larger particle size released 65, 77 and 84% of its nitrate in 1, 3 and 7 days, respectively. Another anionic clay (synthesized at 175°C/24 hrs) of higher charge density (Mg:Al = 2:1) containing NO3
– was equilibrated with a 0.012 N NaCl or Na2CO3 to test the role of different anions in releasing the NO3
– anion from the interlayers. The results showed that Cl– released more NO3
– than did CO3
2– from this anionic clay after all the treatment times probably as a result of the CO3
2– anion blocking the release of NO3
– from the interior of the crystals. When a lower charge density (Mg:Al = 3:1) sample (synthesized at 175°C/48 hrs) was equilibrated with 0.02N solution of anions the release of nitrate was as follows: Cl– < F– < SO4
= CO3
2–. These results suggest that the divalent SO4
= and CO3
2– anions are more effective in the release of NO3
– from this lower charge density anionic clay. Time-resolved structural analysis of NO3
– exchange with CO3
2– in the above anionic clay using synchrotron x-ray diffraction showed that ion exchange is rapid because of small crystal size and lower charge density. Thus the release of NO3
– from anionic clays is an interplay among the type of anions present in soil solution, their concentration, pH of soil solution, the charge density and crystal size of anionic clay etc. 相似文献
26.
D301树脂分离衣康酸的工艺研究 总被引:1,自引:0,他引:1
采用弱碱性阴离子交换树脂D301对发酵法生产的衣康酸进行了分离研究。通过静态交换实验,研究了D301树脂对衣康酸的静态交换动力学,确定了传质机制和影响因素;通过动态交换实验,研究了以硫酸为洗脱剂,以氨水为再生剂的工艺过程,确定了主要工艺参数。 相似文献
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扩散渗析法从钛白废酸中回收硫酸 总被引:20,自引:0,他引:20
针对钛白废酸的回收,在静态扩散条件下测定了硫酸、硫酸亚铁在阴离子交换膜中的渗析系数以考察膜的分离性能。进一步考察动态扩散操作参数如流量、流量比、停留时间等对回收率及回收酸浓度的影响。研究表明,使用的阴离子交换膜具有良好的分离性能,酸盐分离系数达23.6,在水酸流量比维持在1~1.1,废酸流量维持在0.6L·h-1左右的条件下,硫酸回收率大于85%,硫酸亚铁透过率小于7%。 相似文献
29.
以等摩尔的γ-氨丙基三乙氧基硅烷与γ-氯丙基三乙氧基硅烷于140℃反应12 h,脱盐后再与1.2倍摩尔的γ-氯丙基三乙氧基硅烷150℃反应16 h,得叔胺硅氧烷预聚物,该预聚物在甲苯-甲醇-水混合溶剂中进一步聚合成含N高度交联的有机硅聚硅氧烷树脂骨架.骨架与溴乙烷在120℃的封管反应20 h,生成强碱性阴离子交换树脂(PNC树脂),交换量可达1.55 mmol·g-1.该树脂用碳酸氢根转型后于固定床反应器中在95℃、1.2 MPa、环氧乙烷与水摩尔比18、空速1.0h-1下催化环氧乙烷水合反应,连续运行72 h,环氧乙烷转化率可达96.9%,乙二醇选择性可达97.1%;交换容量损失率小于2%,溶胀率为零. 相似文献
30.
Yu.V. Maksimov M.V. Tsodikov E.A. Trusova I.P. Suzdalev J.A. Navío 《Catalysis Letters》2001,72(1-2):11-15
Peculiarities in catalytic activity in carbon monoxide oxidation as well as some structure, electronic and magnetic properties of the three oxide catalysts, Mn3+–O/Al2O3 (1), Mn3+–O–Fe/Al2O3 (Mn-substituted spinel, 2) and -Fe2O3/Al2O3 (3), were studied by kinetic measurements and by Mössbauer spectroscopy. The catalysts 1 and 2 showed a kinetic bistability with a sharp transition towards more reactive state at 200°C (ignition point). In contrast, for catalyst 3, at 200–250°C, the behavior of reaction rate against temperature did not display noticeable hysteresis. On cooling the catalysts 1 and 2, extinction was observed at about 170 and 120°C, respectively, i.e., at 30–80°C lower than the corresponding ignition points. Proximity of activation energy for the high and low activity (15–19 kJ/mol) for both Mn-containing catalysts suggests an increase in the number of active sites at high temperature with no changes in the reaction mechanism. The considerable difference between Mn-containing catalysts 1, 2 and Fe-containing catalyst 3 may be caused by Jahn–Teller (JT) type distortions of the oxygen polyhedron around Mn3+. A significant spontaneous axial bond stretching within the local polyhedron seems to diminish Mn–O binding energy, facilitate the participation of surface oxygen species, OS, in the oxidation of CO by a redox mechanism and promote oxygen vacancies at the surface that would cause considerable effect on the activity. An increase in the width of the counterclockwise hysteresis loop for the catalyst 2 compared to the catalyst 1 indicates that clusters of mixed spinel provide more active sites and more labile OS species than clusters of the binary Mn oxide. 相似文献