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1.
According to the Food and Agriculture Organization of the United Nations, approximately 1.3 billion tons of food is wasted each year, equivalent to approximately one-third of world production. Agri-food wastes are the source of proteins, carbohydrates, lipids, and other essential minerals that have been exploited for value-added products by the development of biorefineries and sustainable business as important elements of circular economies. The innovation and materialization of these types of processes, including the use of disruptive technologies on microbial bioconversion and enzyme technology, such as nanotechnology, metabolic engineering, and multi-omics platforms, increase the perspectives on the waste valorization process. Lignocellulolytic enzymes, pectinases, and proteases are mainly used as catalyzers on agri-food waste treatment, and their production in house might be the trend in near future for agro-industrial countries. Another way to transform the agri-food wastes is via aerobic or anaerobic microbial process from fungal or bacterial cultures; these processes are the key to produce waste enzymes.  相似文献   
2.
This study aimed to investigate the impact of multi-mode S-type ultrasound treatment on the protein extraction level of walnut dregs. The structural properties of the walnut protein (WP) were characterized, and the correlation between protein structure and extraction level was analyzed. The in situ real-time monitoring model for the ultrasound-assisted WP extraction process was established by a miniature fiber near-infrared (NIR) spectrometer. Results showed that the protein yield, purity, and comprehensive extraction index (CEI) of extracted WP were 71.07 %, 72.69 %, and 71.72, respectively, under optimal conditions (dual-frequency 20/28 kHz, ultrasonic treatment duration 30 min, and ultrasound power density 120 W/L). The secondary structure of extracted WP displayed that the proportion of α-helix and β-sheet reduced, while the contents of β-turn and random coil increased after ultrasonic treatment. Besides, sonication decreased the disulfide bond content and increased free sulfhydryl (-SH) and surface hydrophobicity compared to the control. The microstructures of WP confirmed that appropriate sonication could unfold the protein aggregates and reduce the particle size. The extraction level of WP is positively correlated with the -SH content (p < 0.01). The quantitative prediction model of Si-PLS for -SH content in the ultrasound-assisted WP extraction process was established and performed a good correction and prediction performance (Rc = 0.9736; RMSECV = 0.446 μmol/L; Rp = 0.9342; RMSEP = 0.807 μmol/L). This study exploited a high-efficiency way for the WP extraction industry, and provided theoretical support for the development of the intelligent system in industrial protein extraction process.  相似文献   
3.
Carotenoids are an essential component of cashew and can be used in pharmaceuticals, cosmetics, natural pigment, food additives, among other applications. The present work focuses on optimizing and comparing conventional and ultrasound-assisted extraction methods. Every optimization step took place with a 1:1 (w:w) mixture of yellow and red cashew apples lyophilized and ground in a cryogenic mill. A Simplex-centroid design was applied for both methods, and the solvents acetone, methanol, ethanol, and petroleum ether were evaluated. After choosing the extractor solvent, a central composite design was applied to optimize the sample mass (59–201 mg) and extraction time (6–34 min). The optimum conditions for the extractor solvent were 38% acetone, 30% ethanol, and 32% petroleum ether for CE and a mixture of 44% acetone and 56% methanol for UAE. The best experimental conditions for UAE were a sonication time of 19 min and a sample mass of 153 mg, while the CE was 23 min and 136 mg. Comparing red and yellow cashews, red cashews showed a higher carotenoid content in both methodologies. The UAE methodology was ca. 21% faster, presented a more straightforward composition of extracting solution, showed an average yield of superior carotenoid content in all samples compared to CE. Therefore, UAE has demonstrated a simple, efficient, fast, low-cost adjustment methodology and a reliable alternative for other applications involving these bioactive compounds in the studied or similar matrix.  相似文献   
4.
The present study firstly aimed at developing a multi-residue method to identify and quantify 38 veterinary antibiotics (belonging to five different classes) not only for raw swine wastewater but also for wastewater differently treated by different units. The proposed method is based on a solid-phase extraction procedure and ultra high performance liquid chromatography with mass spectrometry. For sample preparation, the optimal loading sample volume was selected as 50 mL, the pH of which was adjusted to approximately 3.0 using formic acid. Then 0.1 g/L ethylenediaminetetraacetic acid disodium salt was added. The recovery rates for different types of wastewaters were in the range of 35.94–124.51% and the relative standard deviations were in the range of 0.36–14.62%. All the matrix standard curves exhibited high linearity (0.9956–0.9999). The matrix effects for the target antibiotics ranged from –61.73 to +148.75%. To ensure the practicality of the method, we performed the detection of the actually added concentration to determine method detection limits and quantitation limits. The quantitation limits of most of the target antibiotics were 0.04 μg/L, except for spiramycin (0.1 μg/L) and roxithromycin (0.2 μg/L). This optimized and validated method was applied to analyze antibiotic residues in swine water samples from four swine farms.  相似文献   
5.
Recently, pharmaceuticals and personal care products in the water environment exhibited potential risks to both human and aquatic organisms. In order to improve the sensitivity and accuracy of pharmaceutical detection, the polyimidazolyl acetate ionic liquid was synthesized by Radziszewski reaction and coated on cellulose filter papers as a thin-film extraction phase for extraction of non-steroidal anti-inflammatory drugs from water. The attenuated total reflection-infrared spectrometry, thermogravimetric analysis, and scanning electron microscope analyses demonstrated that the polyimidazolyl acetate ionic liquid was successfully prepared and attached to the surface of the cellulose filter paper through chemical bonding. The adsorption capacity of the homemade thin-film extraction material for the four non-steroidal anti-inflammatory drugs was greater than 8898 ng/cm2 under the optimum conditions, and the desorption rate was over 90%. Then, a paper-based thin-film extraction phase-high-performance liquid chromatography-tandem mass spectrometry method was established for the extraction of non-steroidal anti-inflammatory drugs in water. This method provided limits of detection and limits of quantification were in the range of 0.02–0.15 and 0.17–0.50 μg/L, respectively. Hence, the obtained thin-film extraction phase showed excellent recovery and reproducibility for the target non-steroidal anti-inflammatory drugs with carboxyl groups from water.  相似文献   
6.
In this study, we used the Span 80 to enhance solvent extraction process, and we explored the mechanism. The results indicated different solvents would obtain different oil recovery, and toluene showed the optimal oil recovery, and the n-heptane showed the lowest oil recovery. The complex solvents could improve oil recovery. Toluene could make the heavy oil show the lowest viscosity (89.6 Pa.S), and n-heptane make the heavy oil show the highest viscosity (176.3 Pa.S). Complex solvents could decrease the heavy oil viscosities. The higher C/H was, the higher heavy oil recovery was, and when the asphaltene and resins content increase, the C/H would increase. The C/H showed the highest value (9.09, by toluene) and the lowest value (8.15). In this study, Span 80 could increase heavy oil C/H ratio, decrease heavy oil viscosity. Span 80 could make the sands surface more hydrophilic, and then the solvent loss would decrease. The oil recovery was high after 10 times recycle use.  相似文献   
7.
甲氧基多溴联苯醚(methoxypolybrominated diphenyl ethers, MeO-PBDEs)广泛存在于生物体和海洋环境。以象山海域的生物体和沉积物为样本,采用固相萃取净化-气相色谱-负化学源质谱法,检测了6种MeO-PBDEs,结果显示,当目标分析物浓度为0.1~20.0 μg?L-1时,线性关系良好(R2>0.999),检出限为0.13~0.22 μg?kg-1,定量限为0.42~0.72 μg?kg-1,实际样品的平均回收率为71.2%~116.2%。MeO-PBDEs的分布状况调查结果显示,藻类样品中仅检出6-MeO-BDE-47,且浓度较低,其他生物体中检出3种MeO-PBDEs,检出率为31.3%,浓度为0.21~2.72 μg?kg-1。沉积物中无MeO-PBDEs被检出。  相似文献   
8.
水稻分蘖期无人机高光谱影像混合像元特征分析与分解   总被引:1,自引:0,他引:1  
开展水稻无人机高光谱解混,获取水稻植株的高光谱反射率信息,对于提高水稻理化参量的反演模型精度具有重要意义。目前大多基于高光谱遥感影像自身数据进行解混,运用算法模型进行高光谱数据解混,将高光谱图像和可见光图像进行优势互补,提出一种基于无人机高清影像与高光谱遥感影像融合的稻田无人机高光谱解混方法,解决单一数据局限性问题,增强光谱数据对地物的描述能力。为了更好的计算端元丰度,将同一目标区的高清数码正射影像与无人机高光谱遥感影像利用经纬度信息进行空间配准,使得不同传感器获得的图片在几何位置上对齐,通过SVM分类器的监督分类方法对可见光的数码正射影像进行地物分类,利用地物分类的结果对应高光谱的一个像元,从而得到一个像元内的端元丰度。设相邻区域内的水体端元是相同的,利用线性解混模型(LSMM)对相邻区域的混合像元进行解混,最终获取水稻高光谱反射率信息。结果表明对两种图片进行空间配准丰富了数据源信息,有利于像元的端元丰度计算,其中水稻端元丰度在70%以上解混效果最好,丰度在50%以上解混效果一般,丰度在30%以下解混效果较差;选择监督分类方法进行地物分类,精度达到99.5%,面向对象方法分类精度为98.2%,监督分类方法优于面向对象分类方法;最终得到的混合像元分解反射率高于原混合像元反射率,减少了水体混合部分对光谱数据的影响,使得分解后水稻的光谱反射率更加准确,为水稻理化参量无人机成像高光谱遥感反演提供更加准确的科学依据。  相似文献   
9.
This study investigates the potential of using small amounts of ionic liquids (IL) to enhance ultrasound-assisted extraction of lipids content from green microalgae. Three imidazolium-based ILs (butyl, octyl and dodecyl), each of them with two anions (bromide and acetate) were tested as additives. Viscosity and surface tension of the ILs aqueous mixtures were analyzed to determine the influence of ILs’ anions and alkyl chain length, whereas KI dosimetry experiments were used as an indicator of radicals formation. A key finding suggests that the small addition of ILs improves the ultrasonication either by enhancing the viscosity and reducing the water surface tension, leading to a more powerful acoustic cavitation process or by increasing HO° production likely to oxidize the microalgae cells membranes, and consequently disrupting them on a more efficient manner. KI dosimetry also revealed that long ILs alkyl chain is detrimental. This experimental observation is confirmed thus strengthened as the yield of extracted lipids from green microalgae has shown an incremental trend when the IL concentration also increased. These hypotheses are currently under investigation to spot detailed impact of ILs on cavitation process.  相似文献   
10.
From the recent market trend, there is a huge demand for the bioactive compounds from various food matrices that could be capable enough to combat the emerging health effects in day-to-day life. Fenugreek is a well-known spice from ancient times for its medicinal and health benefits. In the present study, two methods of green extraction microwave (MAE) and ultrasound (UAE) assisted were studied in regard of extraction of fenugreek diosgenin. In this study, solvent type (acetone, ethanol, hexane and petroleum ether), solvent concentration (40, 60, 80 and 100%) and treatment time (1.5, 3.0, 4.5 and 6.0 min and 30, 40, 50 and 60 min for MAE and UAE method respectively) was varied to observe the effect of these parameters over extract yield and diosgenin content. The results of this study revealed that treatment time, type of solvent and its concentration and method adopted for extraction of diosgenin has significant effect. In relation with better yield extract and diosgenin content, the yield of fenugreek seed extract was 7.83% with MAE and 21.48% with UAE of fenugreek seed powder at 80% ethanol concentration at 6 and 60 min respectively. The content of diosgenin was observed in fenugreek seed powder extract was 35.50 mg/100 g in MAE and 40.37 mg/100 g in UAE with 80% ethanol concentration at 6 and 60 min respectively. The overall range of yield of fenugreek extract was varied from 1.04% to 32.48% and diosgenin content was 15.82 mg/100 g to 40.37 mg/100 g of fenugreek seed powder including both extraction methods. This study revealed that UAE would impose better ways for preparing fenugreek extract and observing diosgenin content from fenugreek seeds.  相似文献   
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