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101.
ANSYS在低温压力容器应力分析与优化设计中的应用   总被引:7,自引:0,他引:7  
丁昌  汪荣顺 《低温与超导》2007,35(6):455-457
介绍了大型有限元软件ANSYS在低温压力容器典型应力分析(不连续区局部应力分析、热应力分析、接触应力分析、复合材料应力分析)与优化设计中的应用,论证了ANSYS作为低温压力容器应力分析与优化设计有效手段的实用性和可靠性,为低温压力容器的应力分析和优化设计找到了一条新途径。  相似文献   
102.
为了对部分流低温流体(液氮)循环泵空化特性进行预测.基于软件ANSYS-FLUENT,计算选用Stardard k-ε湍流模型,Simplec压力耦合方式,进行空化前MRF模型定常计算,添加两相流参数,选取Singhal-et-al空化模型,添加两相参数,考虑液-气密度比对低温流体液氮泵内能量的传递和交换的影响,得到气液动量、质量和能量守恒方程,利用RNG k-ε湍流模型,Simplec压力耦合方式,对不同进液压力条件下,部分流低温流体(液氮)循环泵空化特性进行全流域空化数值计算.进行泵空化特性试验,在额定转速下,随着泵前流体压力的降低呈现的空化性能,数值计算与试验测得的泵头数值最大偏差在10%以内,曲线吻合性较好,泵内流场空化发生伴有显著的压头下降,空化过程增强,空化区变大,液相和汽相相互拖拽能力增强,空化核心区由叶顶背压部分扩散到整个流道,汽液界面不清晰,直至断流.本文采用的计算方法和研究结果为低温流体循环泵内部流体空化的诊断和性能优化提供了一定依据.  相似文献   
103.
Summary When headspace gas chromatography utilizing capillary columns is used for trace analysis, sample enrichment is often needed. This involves splitless sample injection of fairly large gas volumes and relatively long sampling times. As a result of this, the band of the sample vapor may be too large causing peak distortion and poor resolution. This problem can be easily overcome by the use of cryogenic trapping. While this can be accomplished by cooling the whole column to subambient temperature during sample introduction, a more convenient way is to utilize part of the first coil of the capillary column as a cryogenic trap.The paper discusses the theoretical background and instrumentation of cryogenic trapping and demonstrates the possibilities through a number of examples.Enlarged text of a paper presented at the 37th Pittsburgh Conference on Analytical Chemistry and Applied Spectroscopy, Atlantic City, NJ, March 10–14, 1986.  相似文献   
104.
Data are presented to illustrate putative water effects on the retention times and peak shapes for seven sulfur-containing compounds when determined by sub-ambient FSOT capillary GC/FPD. The observations are consistent with explanations based upon reported “phase soaking” and “reverse solvent effect” phenomena.  相似文献   
105.
106.
Over the last decade, stimuli-responsive microemulsions, that is, those that switch between stable and unstable states in response to certain stimuli, have attracted considerable attention because of their unique properties and potential for diverse applications. Herein, we highlight the recent advances in the development of microemulsions responsive to external triggers such as pH, redox reactions, light, CO2 gas, magnetic field and temperature; discuss the corresponding responses; and reveal important composition–microstructure–macroscopic property relationships to suggest future research directions and potential applications.  相似文献   
107.
Summary A convenient procedure has been described for enhancing the sensitivity of equilibrium headspace gas chromatography. The technique involves the cryogenic focusing of headspace vapors at the head of a 0.32 mm fusedsilica capillary column which has been coupled to a packed column injection port. Cryofocusing is accomplished automatically by cooling the GC oven and results in enhanced sensitivity with improved resolution. With this simple focusing technique no sample splitting is required which gives at least a 10-fold increase in sensitivity. A Multiple Headspace Injection (MHI) technique has been described which allows several rapid headspace injections to be made at the start of a single chromatographic run. Cryofocusing causes the injections to be superimposed, thus increasing the sensitivity even further. These procedures have been demonstrated for flavor and aroma analyses of toothpaste and soft drink samples. Presented at the Symposium on Headspace GC, National American Chemical Society Meeting, Chicago, Ill., September 8–13, 1985  相似文献   
108.
A new configuration for coupling a purge-and-trap unit to a capillary column gas chromatograph via a cryogenic focusing interface has been developed. In this configuration, the precolumn of the cryogenic focusing interface was inserted through the septum of a split/splitless injection port where it served as both sample transfer and carrier gas supply lines. The injection port of the gas chromatograph was modified by plugging the carrier gas and the septum purge lines. This configuration allowed for the desorption of analytes at high flow rates while maintaining low, analytical-column flow rates which are necessary for optimum capillary column operation. The capillary column flow rate is still controlled by the column backpressure regulator. Chromatograms of purgeable aromatics exhibited improved resolution, especially for early eluting components compared to those obtained by direct liquid injection using the normal splitless injection mode. Quantitative sample transfer to the analytical column afforded excellent linearity and reproducibility of compounds studied.  相似文献   
109.
In this work several pre-treatment methods were studied for metal (Na, K, Mg, Cu and Ca) determination in Orujo spirit samples using inductively coupled plasma atomic emission spectrometry (ICP-AES). Dilution, digestion, evaporation, and cryogenic desolvatation techniques were comparatively evaluated. Because of their analytical characteristics, digestion and evaporation with nitrogen current were found to be appropriate procedures for the determination of metals in alcoholic spirit samples. Yet, if simplicity and application time are to be considered, the latter—evaporation in a water bath with a nitrogen current—stands out as the optimum procedure for any further determinations in Orujo samples by ICP-AES. Low detection levels and wide linear ranges (sufficient to determine these metals in the samples studied) were achieved for each metal. The recoveries (in the 97.5-100.5% range) and the precision (R.S.D. lower than 5.6%) obtained were also satisfactory. The selected procedure was applied to determine the content of metals in 80 representative Galician Orujo spirit samples with and without a Certified Brand of Origin (CBO) which had been produced using different distillation systems. The metal concentrations ranged between 0.37 and 79.7 mg L−1 for Na, <LOD to 12.4 mg L−1 for K, 0.02-4.83 mg L−1 for Mg content, <LOD to 37.3 mg L−1 for Cu and 0.03-13.10 mg L−1 for Ca.  相似文献   
110.
Summary A simple and sensitive method is presented for determination of styrene, toluene, ethylbenzene, isopropylbenzene andn-propylbenzene in human body fluids by capillary gas chromatography (GC) with cryogenic oven trapping. After heating a blood or urine sample containing each compound andp-diethylbenzene (internal standard, IS) in a 7.0-mL vial at 60°C for 20 min, 5 mL of headspace vapor was drawn into a glass syringe and injected into a GC. All vapor was introduced into an Rtx-Volatile middle bore capillary column in splitless mode at oven temperature of 20°C to trap entire analytes, and the oven temperature then programmed to 280°C for GC measurements by flame ionization detection. The present conditions gave sharp peaks of each compound and IS, and low background noises for whole blood or urine samples.  相似文献   
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