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111.
Abstract

A computational algorithm is proposed for catalyst pellets or reactors experiencing concentration‐dependent deactivation. In the integration of the deactivation equation in each time interval, the concentration of poison, reactant or/and product is considered to be a constant. The value of concentration is recalculated from the mass balance equation before integrating the deactivation equation. By such an approach, the number of equations is reduced; thus a two‐dimensional problem can be converted to a single‐dimensional one.  相似文献   
112.
In construction scheduling, problems can arise when each activity could start at different time points and the resources needed by the activities are limited. Moreover, activities have required conditions to be met, such as precedence relationships, resource requirements, etc. To resolve these problems, a two-phase GA (genetic algorithm) model is proposed in this paper, in which both the effects of time-cost trade-off and resource scheduling are taken into account. A GA-based time-cost trade-off analysis is adopted to select the execution mode of each activity through the balance of time and cost, followed by utilization of a GA-based resource scheduling method to generate a feasible schedule which may satisfy all the project constraints. Finally, the model is demonstrated using an example project and a real project.  相似文献   
113.
根据CTL发布的DSH 0743决议,归纳了LED节能灯测试标准中的要求,主要包含对灯头、防触电、灯头温升、绝缘材料、异常状态、结构的考核,以及灯的光生物学安全考核。  相似文献   
114.
Abstract

The feasibility analysis of integrating methanol to olefins (MTO) with fluidized catalytic cracking (FCC) process is based on their similarities and compatibility. Feeding methanol in FCC is proposed to produce more light olefins. According to the characters of FCC, the effects of reaction temperature, water co-feed, and the coke content of catalyst in methanol conversion were studied systematically. It is concluded that high light olefins yields from methanol conversion were obtained on the FCC condition. Feeding methanol in FCC at the bottom of riser as the proper position was suggested on the ground of comparison with MGD process of FCC. The research proved the feasibility of feeding methanol in FCC and provided important reference for its commercial application in a certain degree.  相似文献   
115.
As part of continuous efforts to understand the surprising synergetic effect between β‐nucleating agent and pre‐ordered structures of isotactic polypropylene (iPP) in significant enhancement of β‐crystallization (Ordered Structure Effect, OSE), two β‐nucleated iPP with different uniformities of stereo‐defect distribution (WPP‐A and WPP‐B) were prepared, their crystallization behaviors with variation of melt structures were studied in detail. The results revealed that β‐phase can hardly form in WPP‐A (whose stereo‐defect distribution is less uniform) because of its strong tendency of α‐nucleation caused by its less uniform stereo‐defect distribution, while WPP‐B is more favorable for β‐crystallization; As fusion temperature decreases, similar variation trends of crystallization temperature and β‐phase proportion can be observed from WPP‐A and WPP‐B, indicating the occurrence of OSE behavior, which provides unsurpassed β‐nucleation efficiency and induces β‐crystallization even in WPP‐A which is less favorable for β‐crystallization; moreover, the upper and lower limiting temperatures of Region II of WPP‐A and WPP‐B are identical, suggesting the uniformity of stereo‐defect distribution has little influence on temperature window for OSE (denoted as Region II). To explore the physical nature of Region II, self‐nucleation behavior and equilibrium melting temperature of PP‐A and PP‐B were studied. The lower limiting temperatures of exclusive self‐nucleation domain of both PP‐A and PP‐B are identical with the lower limiting temperatures of Region II in OSE (168°C); moreover, the Tm0 of both PP‐A and PP‐B are close to their upper limiting temperatures of Region II in OSE behavior (189°C). The possible explanation was proposed. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42632.  相似文献   
116.
117.
Phase‐change heat‐storage UV curable polyurethane acrylate (PUA) coating was prepared by applying microencapsulated phase change materials (microPCMs) to PUA coating. MicroPCMs containing paraffin core with melamine‐formaldehyde shell were synthesized by in situ polymerization. The effect of stirring speed, emulsification time, emulsifier amount, and core/shell mass ratio on particle size, morphology, and phase change properties of the microPCMs was studied by using laser particle size analyzer, Fourier transform infrared spectroscopy, X‐ray photoelectron spectroscopic analysis, scanning electron microscopy, and differential scanning calorimetry. The results showed that the diameter of the microcapsules decreased with the increase of stirring speed, emulsification time, and emulsifier amount. When the mass ratio of emulsifier to paraffin is 6%, microcapsules fabricated with a core/shell ratio of 75/25 have a compact surface and a mean particle size of 30 μm. The sample made under the above conditions has a higher efficiency of microencapsulation than other samples and was applied to PUA coating. The dispersion of microPCMs in coating and heat‐storage properties of the coating were investigated. The results illustrated that the phase‐change heat‐storage UV curable PUA coating can store energy and insulate heat. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41266.  相似文献   
118.
This study investigates the drivers’ merging behavior and the rear-end crash risk in work zone merging areas during the entire merging implementation period from the time of starting a merging maneuver to that of completing the maneuver. With the merging traffic data from a work zone site in Singapore, a mixed probit model is developed to describe the merging behavior, and two surrogate safety measures including the time to collision (TTC) and deceleration rate to avoid the crash (DRAC) are adopted to compute the rear-end crash risk between the merging vehicle and its neighboring vehicles. Results show that the merging vehicle has a bigger probability of completing a merging maneuver quickly under one of the following situations: (i) the merging vehicle moves relatively fast; (ii) the merging lead vehicle is a heavy vehicle; and (iii) there is a sizable gap in the adjacent through lane. Results indicate that the rear-end crash risk does not monotonically increase as the merging vehicle speed increases. The merging vehicle's rear-end crash risk is also affected by the vehicle type. There is a biggest increment of rear-end crash risk if the merging lead vehicle belongs to a heavy vehicle. Although the reduced remaining distance to work zone could urge the merging vehicle to complete a merging maneuver quickly, it might lead to an increased rear-end crash risk. Interestingly, it is found that the rear-end crash risk could be generally increased over the elapsed time after the merging maneuver being triggered.  相似文献   
119.
120.
The Hansen solubility parameters (HSPs) are useful for predicting solvent–solute affinity. In this study, the HSPs and the sphere radii (Ro's) of poly(ether sulfone), bitumen, and lignin were determined by a novel optimization method. A hybrid algorithm, which could locate multiple optima, was developed and used to solve optimization problems for maximizing the fitness (F) and minimizing both Ro and the numbers of good solvent and total outliers. For most selected samples, improved results with higher F and reduced Ro and number of outliers were obtained. The results clarify the correlations among three criteria for an optimal solubility sphere, namely, the smallest Ro, highest F, and lowest number of outliers. They can be satisfied simultaneously only when outliers are avoided; otherwise, a reduction in Ro decreases F but can retain the same outliers. Thereby, defining the solubility sphere as the one having the smallest Ro and the lowest number of outliers is more reasonable according to the physical significance in both cases. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43328.  相似文献   
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