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排序方式: 共有177条查询结果,搜索用时 15 毫秒
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Soodabeh Davaran Davoud Asgari Mohammad Reza Rashidi Roya Salehi Yadolah Omidi 《应用聚合物科学杂志》2011,119(5):2635-2643
To develop a novel pH‐sensitive PEGylated carrier for protein‐based anticancer agents, we modified bovine serum albumin (BSA) with poly(ethylene glycol) citrate ester (PEG–CA) through amidation with its amino groups. Increasing the mixing ratio of albumin from 3 to 6 with respect to PEG–CA resulted in a 2‐fold increase in the degree of albumin modification. Adriamycin (ADR)‐loaded PEG–CA–BSA hydrogels and microparticles were prepared, and the cumulative amounts of ADR released from the PEG–CA–BSA hydrogels (phosphate‐buffered saline, pH 7.4) showed that all the PEG‐CA‐BSA(x) (x represents degree of substitution of PEG to amino group of albumin, i.e. 26%, 28%, 31% and 49%) hydrogels had lower ADR release rates with a slight initial burst release. During the first 24 h, the cumulative releases were 15.5% for PEG–CA–BSA(49), 24% for PEG–CA–BSA(31), 31% for PEG–CA–BSA(28), and 38% for PEG–CA–BSA(26). Afterward, all the release rates slowed, and they were almost in the following order: PEG–CA–BSA(26) > PEG–CA–BSA(28) > PEG–CA–BSA(31) > PEG–CA–BSA(49). The release rates of ADR from the microparticles were dependent on the amount of glutaraldehyde. According to our findings, a higher PEG–CA/BSA molar ratio led to a reduced cumulative amount of ADR released from the hydrogels, whereas higher release rates were observed for microparticles with a lower amount of BSA in the conjugates in a pH‐dependent manner. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
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Huimin Lian Roya Momen Yudong Xiao Bai Song Xinyu Hu Fangjun Zhu Huaxin Liu Laiqiang Xu Wentao Deng Hongshuai Hou Guoqiang Zou Xiaobo Ji 《Advanced functional materials》2023,33(49):2306060
Metal-organic frameworks (MOFs) have been proposed as novel fillers for constructing polymer solid electrolytes based composite electrolytes. However, MOFs are generally used as passive fillers, in-depth revealing the binding mode between MOFs and polyethylene oxide (PEO), the critical role of MOFs in facilitating Li+ transport in solid electrolytes is full of challenges. Herein, inspired by density functional theory (DFT) the 2D-MOF with rich unsaturated metal coordination sites that can bind the O atom in PEO through the metal–oxygen bond, anchor TFSI− to release Li+, resulting in a remarkable Li+ transference number of 0.58, is reported according well with the experimental results and molecular dynamics (MD) simulation. Impressively, after the introduction of the 2D-MOF, the Li+ can rapidly hop along the benzene ring center within the 2D-MOF plane, and the interface between the benzene ring and PEO can also serve as a fast Li+ migration pathway, delivering multiple ion-transport channels, which present a high ion conductivity of 4.6 × 10−5 S cm−1 (25 °C). The lithium symmetric battery is stable for 1300 h at 60 °C, 0.1 mA cm−2. The assembled lithium metal solid state battery maintains high capacity of 162.8 mAh g−1 after 500 cycles at 60 °C and 0.5 C. This multiple ion-transport channels approach brings new ideas for designing advanced solid electrolytes. 相似文献
176.
Roya Karimi Alavijeh Kamran Akhbari 《Chembiochem : a European journal of chemical biology》2023,24(20):e202300415
One of the strategies for improved therapeutic effects in cancer therapy is combination chemotherapy. In this study, a flexible nano-MOF (Fe-MIL-88B-NH2) was synthesized in a sonochemical process, then co-loaded with α-tocopheryl succinate (TOS) and curcumin (CCM). The anticancer activity of co-loaded Fe-MIL-88B-NH2 (Fe-MIL-88B-NH2/TOS@CCM) against the HeLa cells was compared with that of the single-loaded counterpart (Fe-MIL-88B-NH2@CCM). MTT analysis indicates improved cytotoxicity of Fe-MIL-88B-NH2/TOS@CCM. The data from the cell apoptosis assay indicated more apoptosis in the case of the co-loaded nano-MOF. This study indicates the positive effect of the presence of TOS on enhancing the anticancer effect of Fe-MIL-88B-NH2@CCM to prepare a more efficient drug delivery nanosystem. 相似文献
177.
Shusheng Tao Roya Momen Zheng Luo Yirong Zhu Xuhuan Xiao Ziwei Cao Dengyi Xiong Wentao Deng Youcai Liu Hongshuai Hou Guoqiang Zou Xiaobo Ji 《Small (Weinheim an der Bergstrasse, Germany)》2023,19(15):2207975
Transition metal selenides anodes with fast reaction kinetics and high theoretical specific capacity are expected to solve mismatched kinetics between cathode and anode in Li-ion capacitors. However, transition metal selenides face great challenges in the dissolution and shuttle problem of lithium selenides, which is the same as Li-Se batteries. Herein, inspired by the density functional theory calculations, heterogeneous can enhance the adsorption of Li2Se relative to single component selenide electrodes, thus inhibiting the dissolution and shuttle effect of Li2Se. A heterostructure material (denoted as CoSe2/SnSe) with the ability to evolve continuously (CoSe2/SnSe→Co/Sn→Co/Li13Sn5) is successfully designed by employing CoSnO3-MOF as a precursor. Impressively, CoSe2/SnSe heterostructure material delivers the ultrahigh reversible specific capacity of 510 mAh g−1 after 1000 cycles at the high current density of 4 A g−1. In situ XRD reveals the continuous evolution of the interface based on the transformation and alloying reactions during the charging and discharging process. Visualizations of in situ disassembly experiments demonstrate that the continuously evolving interface inhibits the shuttle of Li2Se. This research proposes an innovative approach to inhibit the dissolution and shuttling of discharge intermediates (Li2Se) of metal selenides, which is expected to be applied to metal sulfides or Li-Se and Li-S energy storage systems. 相似文献