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991.
Burning rate measurements were carried out for ammonium perchlorate/hydroxyl‐terminated polybutadiene (AP/HTPB) composite propellants with iron (Fe) nanoparticles as additives. Experiments were performed in a strand burner at pressures from 0.2 to 10 MPa for propellants containing approximately 80 % AP and Fe nanoparticles (60–80 nm) at concentration from 0 to 3 % by weight. It was found that the addition of 1 % Fe nanoparticles increased burning rate by factors of 1.2–1.6. Because Fe nanoparticles are oxidized on the surface and have high surface‐to‐volume ratio, they provide a large surface area of Fe2O3 for AP thermal decomposition catalysis at the burning propellant surface, while also providing added energy release due to the oxidation of nanoparticle sub‐shell Fe. The increase in burning rate due to Fe nanoparticle content is similar to the increase in burning rate caused by the addition of iron oxide (Fe2O3) particles observed in prior literature.  相似文献   
992.
Brittle failure is often influenced by difficult to measure and variable microstructure‐scale stresses. Recent advances in photoluminescence spectroscopy (PLS), including improved confocal laser measurement and rapid spectroscopic data collection have established the potential to map stresses with microscale spatial resolution (< 2 μm). Advanced PLS was successfully used to investigate both residual and externally applied stresses in polycrystalline alumina at the microstructure scale. The measured average stresses matched those estimated from beam theory to within one standard deviation, validating the technique. Modeling the residual stresses within the microstructure produced qualitative agreement in comparison with the experimentally measured results. Microstructure scale modeling is primed to take advantage of advanced PLS to enable its refinement and validation, eventually enabling microstructure modeling to become a predictive tool for brittle materials.  相似文献   
993.
Fully conjugated donor–acceptor block copolymers are established as model systems to elucidate fundamental mechanisms of photocurrent generation in organic photovoltaics. Using analysis of steady‐state photoluminescence quenching, exciton dissociation to a charge transfer state within individual block copolymer chains is quantified. By making a small adjustment to the conjugated backbone, the electronic properties are altered enough to disrupt charge transfer almost entirely. Strong intermolecular coupling of the electron donor is introduced by synthesizing block copolymer nanoparticles. Transient absorption spectroscopy is used to monitor charge generation in block copolymer isolated chains and nanoparticles. While efficient charge transfer is observed in isolated chains, there is no indication of complete charge separation. In the nanoparticles, long‐lived polarons are observed as early as ≈15 ns. Thus, aggregation of electron donors can facilitate efficient charge generation.  相似文献   
994.
Kinetic models have been developed to understand the manufacturing of polymeric foams, which evolve from low viscosity Newtonian liquids, to bubbly liquids, finally producing solid foam. Closed‐form kinetics are formulated and parameterized for PMDI‐10, a fast curing polyurethane, including polymerization and foaming. PMDI‐10 is chemically blown, where water and isocyanate react to form carbon dioxide. The isocyanate reacts with polyol in a competing reaction, producing polymer. Our approach is unique, although it builds on our previous work and the polymerization literature. This kinetic model follows a simplified mathematical formalism that decouples foaming and curing, including an evolving glass transition temperature to represent vitrification. This approach is based on IR, DSC, and volume evolution data, where we observed that the isocyanate is always in excess and does not affect the kinetics. The kinetics are suitable for implementation into a computational fluid dynamics framework, which will be explored in subsequent articles. © 2017 American Institute of Chemical Engineers AIChE J, 63: 2945–2957, 2017  相似文献   
995.
996.
In recent years, much research effort has been driven to develop alternative plasticizers for medical and commodity plastic materials. In this study, a modified natural plasticizer, synthesized by esterification of rice fatty acids, was modified by epoxidation with peroxy acid generated in situ. Two natural epoxidized plasticizers were obtained, using peracetic acid (NP‐Ac) and peroctanoic acid (NP‐Oc) as reagent. PVC films after addition of these natural epoxidized plasticizers presented fairly good incorporation and plasticizing performance, as demonstrated by results of mechanical properties, Tg values (as shown by DSC), optical microscopy, exudation, and migration tests, FTIR and X‐ray diffraction obtained for plasticized PVC films. NP‐Ac plasticizer presented enhanced plasticizing performance compared with NP‐Oc, probably due to a higher epoxidation degree obtained in the reaction with peracetic acid. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   
997.
1H‐15N‐13C correlation NMR spectroscopy techniques developed to identify and characterize co‐polymer fragments in melamine‐urea‐formaldehyde (MUF) and phenol‐urea‐formaldehyde (PUF) model systems have been applied to industrially prepared MUF, PUF, and phenol‐melamine‐formaldehyde (PMF) resins. The NMR data confirm that co‐polymers form in a commercially prepared MUF resin manufactured by Momentive Specialty Chemicals Pty. Ltd. Spectra from PUF model reactions were compared with those from a PUF resin and it was determined that PUF co‐polymers did not form in the resin prepared using typical temperature and pH. Finally, NMR spectroscopy was used to identify and characterize PMF co‐polymer bonds in a phenol‐melamine‐urea‐formaldehyde (PMUF) resin prepared using a procedure from Momentive Specialty Chemicals Pty. Ltd. With these NMR techniques in hand, it is now possible to relate co‐polymer structures to properties of commercial thermosets. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   
998.
In this study, we compared a high performance liquid chromatography coupled to inductively coupled plasma mass spectrometry (HPLC-ICP-MS) method and an isotope dilution gas chromatography mass spectrometry (ID-GC-MS) method for the analysis of methylmercury (MeHg) in fish samples. Using HPLC-ICP-MS, the limit of detection (LOD) was 2.0 ngHg?·?g?1 for inorganic Hg and was 5.0 ngHg?·?g?1 for MeHg. In comparison, the LOD for MeHg was 3.4 ngHg?·?g?1 for using ID-GC-MS. Certified reference material (CRM) results agreed well with certified values for both methods. The mean recovery for analysis of CRM BCR 463 by HPLC-ICP-MS was 99?±?2.1 % for MeHg and was 103?±?2.1 % for total Hg. Two CRMs, BCR 463 and CRM DORM2, were analyzed by ID-GC-MS, the mean recovery of MeHg was 87?±?1.9 % for BCR 463, and the mean recovery of MeHg was 102?±?2.9 % for CRM DORM2. Matrix samples spiked with Hg or MeHg at various concentrations were analyzed by two methods. For HPLC-ICP-MS method, the mean recovery for MeHg spiked samples was 93?±?4.2 %. For ID-GC-MS method, the mean recovery for MeHg spiked samples was 91?±?5.2 %. A total of 19 predatory fish and 54 tuna fish samples were analyzed using both methods. No significant difference was observed between the MeHg data generated from both methods. The average relative standard deviation (RSD) between the two datasets for 19 predatory fish samples was 8.8 %. The average RSD between two datasets for 54 tuna fish samples was 4.4 %.The HPLC-ICP-MS method offers substantial advantages over the method of ID-GC-MS because the former method can determine the total mercury (Hg) and MeHg in a single chromatographic run and the analysis time is much shorter. The latter method is time consuming due to overnight digestion and having to conduct presample analysis for signal-matched isotope dilution spiking and requires more expensive isotope labeled reagents.  相似文献   
999.
This study examined associations between changes in sibling relationships and changes in parental differential treatment and corresponding changes in children's adjustment. One hundred thirty-three families were assessed at 3 time points. Parents rated children's externalizing problems, and children reported on sibling relationship quality, parental differential treatment, and depressive symptoms. On average, older siblings were 10, 12, and 16 years old, and younger siblings were 8, 10, and 14 years old at Waves 1, 2, and 3, respectively. Results from hierarchical linear modeling indicated that as sibling relationships improved over time, children's depressive symptoms decreased over time. In addition, as children were less favored over their siblings over time, children's externalizing problems increased over time. Findings highlight the developmental interplay between the sibling context and children's adjustment. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   
1000.
Researchers know relatively little about how family relationships influence work involvement, although individuals are concerned about how family life interferes with or enhances work experiences. This study examined change in parents' work involvement as a function of relationship quality with offspring (mean age = 15 years) with data from 191 families participating in a longitudinal study. Results suggested a compensatory association between parents' feelings of acceptance and warmth toward offspring and work involvement. Less positive acceptance predicted (a) increasing emotional job involvement for mothers with sons and fathers with daughters and (b) increasing work hours for fathers with daughters. Results highlight how parents may compensate for less positive relationships with adolescents and are discussed in terms of research and applied implications. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   
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