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1.
The ultrasound-assisted extraction (UAE) was conducted using the stainless steel (SS) and polyether ether ketone (PEEK) columns and analyzed with high-performance liquid chromatography (HPLC) to understand the mechanism of ultrasound-assisted chromatography (UAC). Empty SS and PEEK columns were used to extract dyes from a fabric under identical conditions with several parameters including the initial ultrasonic bath temperatures (30 °C and 40 °C), ultrasound power intensities (0, 20, 40, 60, 80, and 100 %), ultrasound operation modes (normal and sweep), and ultrasound frequencies (25 kHz, 40 kHz, and 132 kHz) to compare their extraction capabilities. After 30 min of extraction, the amount of extract was determined by HPLC. The PEEK material was significantly affected by ultrasonic radiation compared to the SS material, especially at a higher temperature (40 °C), power intensity (100 %), and frequency (132 kHz) with sweep mode. At a maximum power density of 45 W/L, the extraction effectiveness ratio of PEEK to SS was in the range of 1.8 - 3.9 depending on the specific frequency, initial temperature, and with or without temperature control. The most optimal ultrasound frequencies, in terms of enhancing extraction effectiveness, are in the order of 132 kHz, 40 kHz, and 25 kHz. Unlike the SS material, the PEEK material was more affected by temperature and acoustic effects under identical conditions, especially at 132 kHz ultrasound frequency. In contrast, at lower frequencies of 40 kHz and 25 kHz, no significant differences in the acoustic effects were observed between the PEEK and SS materials. The findings of this study contribute to elucidating the roles of column materials in UAE and UAC.  相似文献   
2.
Cereals (CE) and pseudocereals (PSCE) play a pivotal role in nourishing the human population. Low-frequency ultrasound (LFUS) modifies the structure of CE and PSCE macromolecules such as starch and proteins, often improving their technological, functional and bioactive properties. Hence, it is employed for enhancing the traditional processes utilized for the preparation of CE- and PSCE-based foods as well as for the upcycling of their by-products. We report recent advances in LFUS treatments for hydration, germination, extraction of bioactive compounds from by-products, and fortification of CEs and PSCE, including kinetic modelling and underlying action mechanisms. Meta-analyses of LFUS influence on compounds extraction and starch gelatinization are also presented. LFUS enhances hydration rate and time lag phase of CE and PSCE, essential for germination, extraction, fermentation and cooking. The germination is improved by increasing hydration, releasing promoters and eliminating inhibitors. Furthermore, LFUS boosts the extraction of phenolic compounds, polysaccharides and other food components; modifies starch structure, affecting pasting properties; causes partial denaturation of proteins, improving their interfacial properties and their peptides availability. Overall, LFUS has an outstanding potential to improve transformation processes and functionalities of CE and PSCE.  相似文献   
3.
Natural deep eutectic solvents (NADESs) are defined as mixtures of certain molar ratios of natural compounds such as sugars, organic acids, amino acids, and organic bases that are abundant in organisms. The melting points of these mixtures are considerably lower than those of their individual ingredients and far below ambient temperature. The first publications on the NADES concept in 2011 created a great expectation regarding their potential as green solvents that could replace conventional organic solvents in a wide range of applications. This was largely because many of the drawbacks of conventional synthetic ionic liquids (ILs) and deep eutectic solvents (DESs), particularly their toxicity and environmental hazards, could be solved using NADESs. Throughout the last 7 years, the interest in NADESs has increased enormously as reflected by the exponential growth of the number of related publications. The research on NADESs has rapidly expanded particularly into the evaluation of the feasibility of their application in diverse fields such as the extraction of (targeted) bioactive compounds from natural sources, as media for enzymatic or chemical reactions, preservatives of labile compounds, or as vehicles of non–water-soluble compounds for pharmaceutical purposes. Along with the exploration of these potential applications, there have been a large number of other studies related to their physicochemical features, the search for new NADESs, the research into the interactions between NADES components or with solutes, the recovery of solutes from NADES solutions, and the ways of circumventing inherent problems of NADESs such as their high viscosity and the consequent difficulties in handling them. This article contains a review of the applications of NADESs as extraction solvents, reaction media, and preservative, providing also a perspective of their future.  相似文献   
4.
建立了稻米中4种砷元素形态的液相色谱-原子荧光光谱联用法(LC-AFS),样品用0.15mol/L的硝酸溶液微波提取50min,提取液经离心分离后,采用Hamilton PRP-X100色谱柱,45mmol/L KH2PO4-5mmol/L Na2HPO4缓冲液为流动相,砷形态4个组分能够在7min内达到基线分离,且无需调pH。优化了氢化物发生条件,使用了更低浓度的载流和还原剂。方法学实验结果表明,各组分在2~10ng/mL范围内线性关系良好,相关系数为0.9988~0.9998,各组分的检出限分别为0.29 ng/mL、0.47 ng/mL、0.62 ng/mL和1.16 ng/mL;各组分峰面积的相对标准偏差均低于3.11%;加标回收率为85.3%~112.8%;对稻米标准物质的分析测定结果表明该方法定值准确。最后,与GB 5009.11-2014中使用的提取及测量条件进行对比,表明该方具备法快速、环保、高效的特点。  相似文献   
5.
Neomangiferin (NMF) is an extremely special xanthone that could be simultaneously attributed to C-glycoside and O-glycoside with a variety of biological activities, such as anti-inflammatory, antitumor, antipyretic, and so on. So far as we know, the metabolism profiling has been insufficient until now. Herein, Drug Metabolite Cluster Centers (DMCCs)-based Strategy has been developed to profile the NMF metabolites in vivo and in vitro. Firstly, the DMCCs was proposed depending on literature-related and preliminary analysis results. Secondly, the specific metabolic rule was implemented to screen the metabolites of candidate DMCCs from the acquired Ultra High Performance Liquid Chromatography Quadrupole Exactive Orbitrap Mass Spectrometry (UHPLC-Q-Exactive Orbitrap MS) data by extracted ion chromatography (EIC) method. Thirdly, candidate metabolites were accurately and tentatively identified according to the pyrolysis law of mass spectrometry, literature reports, comparison of reference substances, and especially the diagnostic product ions (DPIs) deduced preliminarily. Finally, network pharmacology was adopted to elucidate the anti-inflammatory action mechanism of NMF on the basis of DMCCs. As a result, 3 critical metabolites including NMF, Mangiferin (MF) and Norathyriol (NA) were proposed as DMCCs, and a total of 61 NMF metabolites (NMF included) were finally screened and characterized coupled with 3 different biological sample preparation methods including solid phase extraction (SPE), acetonitrile precipitation and methanol precipitation. Among them, 32 metabolites were discovered in rat urine, 30 in rat plasma, 12 in rat liver, 9 metabolites in liver microsomes and 8 in rat faeces, respectively. Our results also illustrated that NMF primarily underwent deglucosylation, glucuronidation, methylation, sulfation, dihydroxylation and their composite reactions in vivo and in vitro. Additionally, network pharmacology analysis based on DMCCs revealed 85 common targets of disease-metabolites, and the key targets were TNF, EGFR, ESR1, PTGS2, HIF1A, IL-2, PRKCA and PRKCB. They exerted anti-inflammatory effects mainly through the pathways of inflammatory response, calcium-dependent protein kinase C activity, nitrogen metabolism, pathways in cancer and so on. In general, our study constructed a novel strategy to comprehensive elucidate the biotransformation pathways of NMF in vivo and in vitro, and provided vital reference for further understanding its anti-inflammatory action mechanism. Moreover, the established strategy could be generalized to the metabolism and action mechanism study of other natural products.  相似文献   
6.
环境类雌激素作为食品中一类典型的污染物,严重影响人体内分泌系统的功能与代谢。磁性固相萃取因其简洁高效、富集倍数高、适用范围广等优点,已被广泛应用于食品中环境类雌激素的富集检测。Fe_(3)O_(4)纳米粒子作为经典的磁固相萃取材料,易于形成大分子团聚物,影响其选择吸附性能,限制了磁固相萃取技术在食品中环境类雌激素的痕量分析。新兴的磁性复合材料可有效地解决上述问题,已成为磁固相萃取技术的研究热点之一。本文综述了近5年来新兴的磁性聚合物复合材料、磁性碳基复合材料和磁性金属-有机骨架复合材料在食品中环境类雌激素富集检测的应用进展。  相似文献   
7.
The extraction of UO2(NO3)2 from aqueous solution was investigated using trioctylphosphine oxide (TOPO) and tributylphosphine oxide (TBPO) in ionic liquids (ILs) (CnmimNTf2, n=2, 4, 6, 8). A third phase was formed in the TOPO-C2mimNTf2 and TOPO-C4mimNTf2 extraction systems, whereas the extracted species of TBPO-CnmimNTf2 (n=2, 4, 6, 8) were well soluble in all ILs. The influence of the concentrations of the extractant, nitric acid, and salt on the extraction efficiency was also investigated. Adding HNO3 to the aqueous phase decreased the extraction efficiency. The effect of salt indicates the presence of a cation-exchange mechanism in the extraction. The addition of NO3 - in the aqueous phase increased the extraction efficiency of U, which indicates that NO3 - participates in the extraction. Selective extraction research indicates that TBPO-C4mimNTf2 exhibits good selectivity for U at low acid concentration despite the significant extraction efficiency on Zr at high acid concentration. After removing U, TBPO-C4mimNTf2 still showed high selectivity for Nd at low acid concentration. We also confirmed the difference of the extraction mechanisms among TBPO-CnmimNTf2 by quantitative measurement of NNO3 - in ILs, electrospray ionization mass spectroscopy (ESI- MS), and UV spectroscopy. There are two extraction species (UO2(TBPO)3(NO3)+ and UO2(TBPO)32+) and the proportion of UO2(TBPO)3(NO3)+ increases from C2mimNTf2 to C8mimNTf2.  相似文献   
8.
《Arabian Journal of Chemistry》2020,13(10):7289-7301
Black pepper oils have been investigated frequently in the recent years. However, there is a significant variation in physicochemical properties and bioactivity of oils depended on extraction techniques. In this study, the systemic investigation of four various extraction methods was performed to evaluate the physicochemical characterizations, antioxidant and antibacterial activity. The investigation of 1H NMR, FTIR and UV–Vis spectra confirmed presence of non-volatile components in oils extracted through supercritical CO2 and hexane-soaking extractions which induced their typical thermal properties. The isothermal behaviour of extracted oils related to evaporation was within range of 3.2–7.3% (w/w) at 27 °C. The SEM images of the black pepper confirmed different operation manners of mechanism between extractions using the solvents and heating process. The lowest MIC for both essential oils from conventional hidrodistillation and microwave-assisted hidrodistillation against two bacteria including E. coli and B. subtilis were found to be 137 µg mL−1. The non-isothermal decomposition kinetics were investigated on the essential oil of microwave-assisted hydrodistillation extraction. The activation energies and pre-exponent factors of non-isothermal decomposition were found to be in range of 36.5–73.7 KJ mol−1 and 4.98 × 103–1.97 × 108 s−1, respectively, dependent on conversional fractions of the oil. The results revealed that chemical components, physicochemical properties and bioactivity of black pepper essential oils depended on the extraction techniques.  相似文献   
9.
随着生活水平的不断提高,城市植被已成为衡量城市宜居性的重要标准之一,对城市生物多样性评估和保护起到非常重要的作用。因此,合理规划城市植被是解决环境问题和提高生活质量的重要手段。因此,城市植被的提取和监测成为重中之重的任务。目前,城市植被提取一方面受到地域和物种的影响,另一方面也受到地形和建筑物阴影的影响。为解决上述问题,提出了一种结合数字高程模型(DEM)的红边-近红外植被指数模型(RENVI)。首先选取了3景经过辐射定标和大气校正的具有红边波段、且光谱和空间分辨率较高的Worldview-3遥感影像;然后,根据红边波段对于植被具有较高的敏感性,且红边范围内的光谱数据与反映植被生长状况的参数有较好的相关关系原理,采用DEM模型和红边波段光谱差异,有效去除地形和建筑物阴影;最后,在可见光波段范围内建立红边光谱-近红外光谱构建特征空间,构建了红边-近红外植被指数模型,同时与归一化植被指数(NDVI)和增强型植被指数(EVI)进行城市植被提取的定性和定量对比分析。定性分析是利用真实植被影像参考图与模型提取植被影像进行视觉分析;后者是采用用户精度、生产者精度、总体精度和Kappa系数进行量化分析。定性分析表明:NDVI和EVI提取城市植被,由于建筑和道路像元混淆在植被中,产生了错分和漏分的问题。RENVI较好地消除了阴影像元与植被像元混淆问题,能准确的提取城市植被,减少了冗余度,增加了植被指数的信息量。定量分析表明:RENVI模型较NDVI和RVI能够准确提取城市植被,3景影像总体精度分别为89%,81.4%和91.8%,Kappa系数分别为0.852 8,0.791 3和0.905 2。综上所述,该方法有效提高了城市植被提取精度,并取得了较好的提取视觉效果。  相似文献   
10.
(Liquid + liquid) equilibrium (LLE) studies for the extraction of aromatics from alkanes present in the petroleum fractions are important to develop theoretical/semiempirical (liquid + liquid) equilibrium models, which are used in the design of extraction processes. In this work, the ionic liquid 1-ethyl-3-methylimidazolium methylsulfate, [EMim][MSO4], was evaluated as potential solvent for the separation of toluene from heptane and cyclohexane. The LLE data for the quaternary system {heptane (1) + cyclohexane (2) + toluene (3) + [EMim][MSO4] (4)} were experimentally determined at T = 298.15 K and atmospheric pressure. Moreover, the LLE data for the ternary systems {heptane or cyclohexane (1) + toluene (2) + [EMim][MSO4] (3)} were also determined. Solute distribution ratios and selectivities were calculated and analysed in order to evaluate the capability of the ionic liquid to accomplish the separation target. A comparison between the solute distribution ratios and selectivities for the quaternary and the ternary systems was also made. Finally, the experimental tie-line data were correlated with the NRTL model.  相似文献   
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