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81.
Marco W.M. van Goethem Simon Barendregt Johan Grievink Peter J.T. Verheijen Mario Dente Eliseo Ranzi 《Chemical Engineering Research and Design》2013
Current generation steam cracking plants are considered to be mature. As a consequence it is becoming more and more important to know whether the underlying mechanistic cracking process offers still scope for further improvements. The fundamental kinetic limits to cracking yields have recently been researched in detail for different feed stocks with a new synthesis reactor model, d-RMix, incorporating a large scale mechanistic reaction scheme, SPYRO® [M.W.M. van Goethem, S. Barendregt, J. Grievink, J.A. Moulijn, P.T.J. Verheijen “Model-based, thermo-physical optimisation for high olefin yield in steam cracking reactors”, Chemical Research and Engineering Developments 88 (2010) 1305–1319]. Mathematical optimization revealed for ethane cracking a maximum ethylene yield of about 67 wt%. with a linear-concave optimal temperature profile along the reaction coordinate with a maximum temperature between 1200 and 1300 K. Further mechanistic analysis of these results showed that the linear-concave shape not only suppresses the successive dehydrogenation and condensation reactions of ethylene, but mainly reduces the role of the ethane initiation reaction to form two methyl radicals. 相似文献
82.
Lan Ma Robert Landsiedel A. Kuhlow W. Engst Albrecht Seidel Hansruedi Glatt 《Polycyclic Aromatic Compounds》2013,33(1-4):135-149
The carcinogen 1-methylpyrene (MP) is metabolized via 1-hydroxymethylpyrene (HMP) to a sulfuric acid ester (SMP), which can covalently bind to nucleophiles such as glutathione and DNA. These primary reaction products may be processed to 1-methylpyrenyl mercapturic acid (MPMA) and free nucleoside adducts [e.g. N 2?(1-methylpyrenyl)-deoxyguanosine, MPdG], and then be excreted. MPMA may be considered as a marker for the amount of SMP which was detoxified, whereas MPdG represents that part which underwent uncontrolled reactions with tissue constituents. We have designed sensitive HPLC-MS/MS methods to determine levels of MPMA and MPdG in biological samples. Shortly after administration of HMP to rats, MPMA was detected in blood and was then excreted in urine (> 70 %) and feces (> 30 %), chiefly within 24 h. The level of urinary MPMA was higher in females than in males. MPdG was detected in urine of rat treated with SMP. Future investigations will focus on factors which modify the ratio of the excreted amounts of MPdG and MPMA in animals treated with MP or its metabolites. 相似文献
83.
William M. Baird Louisa A. Hooven Brinda Mahadevan Andreas Luch Albrecht Seidel Patrick L. Iversen 《Polycyclic Aromatic Compounds》2013,33(3-4):771-780
Benzo[ a ]pyrene (B[ a ]P) and dibenzo[ a,l ]pyrene (DB[ a,l ]P) induce cytochrome P450 (CYP) CYP1A1 and CYP1B1, which metabolize these polycyclic aromatic hydrocarbons (PAHs) into DNA-binding species. In order to detail roles of CYP1A1 and CYP1B1 in activation of DB[ a,l ]P to the diol epoxide, we here report the inhibition of CYP1A1 in human MCF-7 cells with phosphorodiamidate morpholino antisense oligomers (morpholinos). PAH-DNA adduct formation was also determined after treatment with morpholinos and B[ a ]P or DB[ a,l ]P. p53 is involved in DNA repair, cell cycle arrest, and apoptosis. Cells with normal p53 protein arrest in the G1 phase of the cell cycle on exposure to DNA-damaging agents (presumably allowing the cell sufficient time to repair damaged DNA prior to replication). Previous studies in human MCF-7 cells indicate that cells with PAH-DNA adducts escape cell cycle arrest and accumulate in the S phase. In the present study the effect of PAH-DNA adducts on the cell cycle were observed in human diploid fibroblasts (HDF). We found that treatment of HDF with the diol epoxide of DB[ a,l ]P causes cell cycle arrest in G 1 . An increase in DNA adduct formation with increase in concentration of dibenzo[ a,l ]pyrene diol epoxide {( m )- anti -DB[ a,l ]PDE} was also observed. 相似文献
84.
Andreas Luch Albrecht Seidel Hansruedi Glatt Franz Oesch Karl L. Platt 《Polycyclic Aromatic Compounds》2013,33(1-4):101-108
In vitro studies on the hepatic biotransformation of the enantiomeric trans-11,12-dihydrodiols of dibenzo[a,l]pyrene (DB[a,l]P) using microsomal fractions of animals pretreated with Aroclor 1254 revealed that the formation of fjord-region dihydrodiol epoxides strongly depends on the absolute configuration of the substrate. Both the (-)-11R,12R- and the (+)-11S,12S-enantiomer are converted diastereoselectively to the (-)- and (+)-anti-dihydrodiol epoxide, respectively, by either rat or mouse liver microsomes. Fjord-region oxidation occurs to greatest extent on incubation of the (-)-11R,12R-dihydrodiol with preparations from rats. This finding is in line with the differences seen for the two enantiomers on the total DNA binding under identical activation conditions as well as on the mutagenic activity in Chinese hamster V79 cells using the postmitochondrial hepatic fraction of Aroclor 1254-treated rats as metabolizing system. 相似文献
85.
Valeri?NaydenovEmail author Lubomira?Tosheva Johan?Sterte 《Journal of Porous Materials》2005,12(3):193-199
Self-bonded zeolite Beta/MCM-41 composite spheres were prepared using a two-step synthesis procedure. In the first step, mesoporous zeolite Beta spheres were obtained using anion exchange resin as macrotemplate. In the second step, the MCM-41 or Al-MCM-41 was grown both on sphere surfaces and in the pore structure of the pre-formed zeolite Beta spheres. Finally, the templating agents used in the synthesis of mesophase were removed by calcination leaving behind self-bonded Beta/MCM-41 composite spheres. Beta/MCM-41 composites were characterized by XRD, SEM and nitrogen adsorption measurements. Materials with controlled macroshape, composition and complex porosity were prepared by the approach. 相似文献
86.
Per Johan Råsmark Čestmír Koňák Petr Štěpánek Christer Elvingson 《Polymer Bulletin》2005,54(4-5):335-342
Summary Dynamic light scattering was used to investigate the dynamics of sodium poly(styrene sulfonate) and fully neutralized poly(acrylic acid) gels as a function of the degree of swelling and weight ratio of cross-linking agent. It was shown that the collective diffusion coefficient increases with increasing degree of swelling and that the diffusion coefficient shows stronger concentration dependence than predicted by scaling arguments. For gel samples measured at the swelling equilibrium, the diffusion coefficient increases with increasing gel concentration for both gel systems. 相似文献
87.
88.
Andrea Snchez-Navarro Miguel ngel Martínez-Rojas Adrin Albarrn-Godinez Rosalba Prez-Villalva Johan Auwerx Abigail de la Cruz Lilia G. Noriega Florencia Rosetti Norma A. Bobadilla 《International journal of molecular sciences》2022,23(5)
Acute kidney injury (AKI) is a public health problem worldwide. Sirtuins are a family of seven NAD+-dependent deacylases, Overexpression of Sirtuin 1, 3, and 5 protect against AKI. However, the role of Sirtuin 7 (Sirt7) in AKI is not known. Here, we analyzed how Sirt7 deficient mice (KO-Sirt7) were affected by AKI. As expected, wild-type and Sirt7 heterozygotes mice that underwent renal ischemia/reperfusion (IR) exhibited the characteristic hallmarks of AKI: renal dysfunction, tubular damage, albuminuria, increased oxidative stress, and renal inflammation. In contrast, the KO-Sirt7+IR mice were protected from AKI, exhibiting lesser albuminuria and reduction in urinary biomarkers of tubular damage, despite similar renal dysfunction. The renoprotection in the Sirt7-KO+IR group was associated with reduced kidney weight, minor expression of inflammatory cytokines and less renal infiltration of inflammatory cells. This anti-inflammatory effect was related to diminished p65 expression and in its active phosphorylation, as well as by a reduction in p65 nuclear translocation. Sirt7 deficient mice are protected from AKI, suggesting that this histone deacetylase promotes tubular damage and renal inflammation. Therefore, our findings indicate that Sirt7 inhibitors may be an attractive therapeutic target to reduce NFκB signaling. 相似文献
89.
Mun Fai Loke Indresh Yadav Teck Kwang Lim Johan R. C. van der Maarel Lok-To Sham Vincent T. Chow 《International journal of molecular sciences》2022,23(6)
The presence of co-infections or superinfections with bacterial pathogens in COVID-19 patients is associated with poor outcomes, including increased morbidity and mortality. We hypothesized that SARS-CoV-2 and its components interact with the biofilms generated by commensal bacteria, which may contribute to co-infections. This study employed crystal violet staining and particle-tracking microrheology to characterize the formation of biofilms by Streptococcus pneumoniae and Staphylococcus aureus that commonly cause secondary bacterial pneumonia. Microrheology analyses suggested that these biofilms were inhomogeneous soft solids, consistent with their dynamic characteristics. Biofilm formation by both bacteria was significantly inhibited by co-incubation with recombinant SARS-CoV-2 spike S1 subunit and both S1 + S2 subunits, but not with S2 extracellular domain nor nucleocapsid protein. Addition of spike S1 and S2 antibodies to spike protein could partially restore bacterial biofilm production. Furthermore, biofilm formation in vitro was also compromised by live murine hepatitis virus, a related beta-coronavirus. Supporting data from LC-MS-based proteomics of spike–biofilm interactions revealed differential expression of proteins involved in quorum sensing and biofilm maturation, such as the AI-2E family transporter and LuxS, a key enzyme for AI-2 biosynthesis. Our findings suggest that these opportunistic pathogens may egress from biofilms to resume a more virulent planktonic lifestyle during coronavirus infections. The dispersion of pathogens from biofilms may culminate in potentially severe secondary infections with poor prognosis. Further detailed investigations are warranted to establish bacterial biofilms as risk factors for secondary pneumonia in COVID-19 patients. 相似文献
90.