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101.
The apparent reduction of β-glucan (BG) molecular weight in rice-based gluten-free (GF) breads fortified with cereal BG concentrates reveals the presence of β-glucanase activity in rice flour. Inactivation of endogenous β-glucanase in rice flour thus seems to be a necessary step when developing GF breads enriched with BG of high molecular weight. The aim of this work was to study the thermal inactivation of endogenous β-glucanase in rice flour by means of microwave (MW) processing; rice flours preconditioned at four different moisture levels (13, 16, 19, 25 %) were treated by MW radiation at 900 W and five MW treatment times (ranging from 40 s to 8 min, applied stepwise at 20-s intervals). The effects of microwaves on starch crystallinity, pasting, and thermal properties of MW-treated rice flours were also explored. The β-glucanase activity in rice flours was assessed by the rate of decrease in specific viscosity of a dilute solution of a purified β-glucan preparation, upon addition of flour extracts. MW proved to be a useful alternative for thermal inactivation of endogenous β-glucanase in rice flours when applied to moistened samples. The inactivation process followed a first-order kinetic response and the apparent rate constant of thermal inactivation increased exponentially with the moisture content of the flour, M, according to the equation 0.0146·exp (0.212·M) (R 2?=?0.97). The MW time required for complete β-glucanase inactivation was only 4 min when the initial flour moisture increased to 25 %. Following MW treatment, the starch crystallinity was unaffected (p?>?0.05) and the side effects of the treatment on flour pasting and thermal properties were rather negligible.  相似文献   
102.
The selective catalytic reduction of NO by H2 under strongly oxidizing conditions (H2-SCR) in the low-temperature range of 100–200 °C has been studied over Pt supported on a series of metal oxides (e.g., La2O3, MgO, Y2O3, CaO, CeO2, TiO2, SiO2 and MgO-CeO2). The Pt/MgO and Pt/CeO2 solids showed the best catalytic behavior with respect to N2 yield and the widest temperature window of operation compared with the other single metal oxide-supported Pt solids. An optimum 50 wt% MgO-50wt% CeO2 support composition and 0.3 wt% Pt loading (in the 0.1–2.0 wt% range) were found in terms of specific reaction rate of N2 production (mols N2/gcat s). High NO conversions (70–95%) and N2 selectivities (80–85%) were also obtained in the 100–200 °C range at a GHSV of 80,000 h−1 with the lowest 0.1 wt% Pt loading and using a feed stream of 0.25 vol% NO, 1 vol% H2, 5 vol% O2 and He as balance gas. Addition of 5 vol% H2O in the latter feed stream had a positive influence on the catalytic performance and practically no effect on the stability of the 0.1 wt% Pt/MgO-CeO2 during 24 h on reaction stream. Moreover, the latter catalytic system exhibited a high stability in the presence of 25–40 ppm SO2 in the feed stream following a given support pretreatment. N2 selectivity values in the 80–85% range were obtained over the 0.1 wt% Pt/MgO-CeO2 catalyst in the 100–200 °C range in the presence of water and SO2 in the feed stream. The above-mentioned results led to the obtainment of patents for the commercial exploitation of Pt/MgO-CeO2 catalyst towards a new NOx control technology in the low-temperature range of 100–200 °C using H2 as reducing agent. Temperature-programmed desorption (TPD) of NO, and transient titration of the adsorbed surface intermediate NOx species with H2 experiments, following reaction, have revealed important information towards the understanding of basic mechanistic issues of the present catalytic system (e.g., surface coverage, number and location of active NOx intermediate species, NOx spillover).  相似文献   
103.
This paper presents a new practical bit-vector algorithm for solving the well-known Longest Common Subsequence (LCS) problem. Given two strings of length m and n, nm, we present an algorithm which determines the length p of an LCS in O(nm/w) time and O(m/w) space, where w is the number of bits in a machine word. This algorithm can be thought of as column-wise “parallelization” of the classical dynamic programming approach. Our algorithm is very efficient in practice, where computing the length of an LCS of two strings can be done in linear time and constant (additional/working) space by assuming that mw.  相似文献   
104.
This paper considers the synthesis of refrigeration systems with refrigerant mixtures as working fluids. The employed refrigeration topology encompasses features from industrial liquefaction of natural gas (LNG) systems. This configuration consists of a combination of horizontal and vertical cascades generalizing the vertical cascade of pure refrigerant systems. The key features of mixtures exploited here are their ability to evaporate/condense over a temperature range and their potential to generate streams with different compositions through partial condensation. The synthesis problem is formulated and solved as a nonlinear program. The proposed methodology is illustrated using an example of cooling a methane-rich stream.  相似文献   
105.
Mixing during melt-melt blending of segregated polypropylene melt streams in a co-rotating twin screw extruder was experimentally investigated. The mixing limited reaction between two polymer reactive tracers, which are terminally functionalized polyolefin oligomers, was used to determine the mixing performance of a kneading block section. The selected functional groups were succinic anhydride and a primary amine, and Fourier-Transform Infrared Spectrometry (FT-IR) was used to determine the anhydride conversion. In the absence of interfacial tension, the reaction conversion was directly related to the amount of interfacial area generated. Experiments were completed to study the effects of operating conditions, kneading block design, and polymer material properties. The screw speed effect was observed to be non-linear because of competing contributions from shear rate, residence time, channel fill, and viscous heating. The mixing performance of kneading blocks backed by a reverse conveying element was observed to follow the trend of: forward > reverse > neutral. For each kneading block design, the mixing performance decreased with an increase in polymer viscosity.  相似文献   
106.
The mechanism of electrostatic spraying of insulating fluids, such as air or organic solvents, into relatively conductive fluids, such as water, is investigated in this work. Experiments with air sprayed into water through an electrified capillary showed that the pressure inside the capillary increases, reaches a maximum, and then decreases as the applied voltage is increased. The initial pressure increase is due to the electric stress on the fluid interface, while the decrease is due to the Coulombic electrohydrodynamic flow generated near the end of the capillary. It is shown that electric fields can cause simultaneous pumping, spraying, and mixing of fluids. This phenomenon is demonstrated for air and kerosene in water.  相似文献   
107.
This study presents the development of novel submicron super absorbent polymers (SAPs) used as admixtures in cement‐based matrices with significant advantages over conventional products. The produced SAPs were characterized in respect of their morphology and composition, while their water absorption capacity was determined in different electrolyte solutions. The hybrid core‐shell spherical structure of the fabricated materials offered significant compatibility enhancement with cement while the workability of the mixture was maintained. The assessment of the cement‐based composites including SAPs revealed that their flexural strength increased by 78%. Self‐healing/sealing behavior was assessed by monitoring the crack sealing via SEM, elemental analysis of the healing products, and determination of the water absorbance coefficient for different times of treatment. The cement/SAPs composites with a concentration of SAPs 2% by weight of cement exhibited self‐healing/sealing responsive capability when an artificial crack was induced. According to the SEM characterization, the crack demonstrated complete healing for the better part of its length after 28 days of treatment.  相似文献   
108.
This brief perspective overviews amphiphilic polymer co‐networks (APCNs), polymeric chemically crosslinked hydrogels also covalently hosting a hydrophobic segment, conferring upon these materials the important property of internal self‐organization in aqueous environments. APCN synthesis is most conveniently accomplished via the random crosslinking copolymerization of a hydrophilic monomer with a hydrophobic macro‐crosslinker, whereas better structures are attained via the end‐linking of amphiphilic linear ABA triblock copolymers or amphiphilic star diblock copolymers. Microphase‐separated morphologies, translucency‐to‐transparency, biocompatibility, low to moderate aqueous swelling, fair mechanical strength and possible stimulus‐responsiveness constitute the main physicochemical properties of APCNs, with their major commercial application being in silicone hydrogel soft contact lenses. Modeling the swelling, morphological and mechanical behavior of these intriguing materials is an area where more progress is necessary in order to improve our understanding of these networks and facilitate the design of next‐generation APCNs. © 2020 Society of Industrial Chemistry  相似文献   
109.
CpdB is a 3′-nucleotidase/2′3′-cyclic nucleotide phosphodiesterase, active also with reasonable efficiency on cyclic dinucleotides like c-di-AMP (3′,5′-cyclic diadenosine monophosphate) and c-di-GMP (3′,5′-cyclic diadenosine monophosphate). These are regulators of bacterial physiology, but are also pathogen-associated molecular patterns recognized by STING to induce IFN-β response in infected hosts. The cpdB gene of Gram-negative and its homologs of gram-positive bacteria are virulence factors. Their protein products are extracytoplasmic enzymes (either periplasmic or cell–wall anchored) and can hydrolyze extracellular cyclic dinucleotides, thus reducing the innate immune responses of infected hosts. This makes CpdB(-like) enzymes potential targets for novel therapeutic strategies in infectious diseases, bringing about the necessity to gain insight into the molecular bases of their catalytic behavior. We have dissected the two-domain structure of Escherichia coli CpdB to study the role of its N-terminal and C-terminal domains (CpdB_Ndom and CpdB_Cdom). The specificity, kinetics and inhibitor sensitivity of point mutants of CpdB, and truncated proteins CpdB_Ndom and CpdB_Cdom were investigated. CpdB_Ndom contains the catalytic site, is inhibited by phosphate but not by adenosine, while CpdB_Cdom is inactive but contains a substrate-binding site that determines substrate specificity and adenosine inhibition of CpdB. Among CpdB substrates, 3′-AMP, cyclic dinucleotides and linear dinucleotides are strongly dependent on the CpdB_Cdom binding site for activity, as the isolated CpdB_Ndom showed much-diminished activity on them. In contrast, 2′,3′-cyclic mononucleotides and bis-4-nitrophenylphosphate were actively hydrolyzed by CpdB_Ndom, indicating that they are rather independent of the CpdB_Cdom binding site.  相似文献   
110.
When a fault occurs in a process, it slowly propagates within the system and affects the measurements triggering a sequence of alarms in the control room. The operators are required to diagnose the cause of alarms and take necessary corrective measures. The idea of representing the alarm sequence as the fault propagation path and using the propagation path to diagnose the fault is explored. A diagnoser based on hidden Markov model is built to identify the cause of the alarm signals. The proposed approach is applied to an industrial case study: Tennessee Eastman process. The results show that the proposed approach is successful in determining the probable cause of alarms generated with high accuracy. The model was able to identify the cause accurately, even when tested with short alarm sub-sequences. This allows for early identification of faults, providing more time to the operator to restore the system to normal operation.  相似文献   
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