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11.
A. Preiss A. Bauer H.-M. Berstermann S. Gerling R. Haas A. Joos A. Lehmann L. Schmalz K. Steinbach 《Journal of chromatography. A》2009,1216(25):4968-4975
An advanced HPLC-photodiode array detection method for the determination of 12 selected highly polar nitroaromatic compounds in ground water samples of ammunition waste sites has been developed and validated. After solid-phase extraction the limits of detection were in the range 0.1–0.5 μg/l. To prove the applicability of the method to other polar nitroaromatic compounds the retention time of another 32 polar compounds under the specified chromatographic conditions were determined and their UV spectra recorded. To review the method, interlaboratory comparisons were performed with a spiked and a real ground water sample. 相似文献
12.
顶空固相微萃取-气相色谱-质谱法同时测定饮用水源水中24种VOCs 总被引:1,自引:0,他引:1
建立了同时测定饮用水源水中24种挥发性有机物(VOCs)的顶空固相微萃取-气相色谱-质谱法.用75 μm CarboxenTM-Polydimethylsiloxane(CAR-PDMS)固相微萃取柱顶空萃取水样中的VOCs,VOCs用气相色谱-质谱联用仪检测,采用内标法定量.对萃取柱涂层、样品盐度、萃取温度和萃取时间等样品前处理条件进行了优化,VOCs的检出限在0.03~0.31 μg/L之间,线性相关系数r>0.996(二氯甲烷和三氯甲烷除外).对饮用水源水实际水样0.50μg/L和1.00 μg/L两个加标浓度水平的回收率进行了测定,三氯甲烷回收率均值分别为104%和142%,其余VOCs回收率分别为90.0%~120%和88.0%~110%,除二氯甲烷和三氯甲烷外,其余VOCs测定结果的相对标准偏差均小于15.0%(n=6).该方法适用于饮用水源水中挥发性有机物的监测分析. 相似文献
13.
Electrospray ionization mass spectrometric detection of low polar compounds by adding NaAuCl4
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Hiroshi Moriwaki 《Journal of mass spectrometry : JMS》2016,51(11):1096-1102
Liquid chromatography electrospray ionization mass spectrometry (LC/ESI/MS) has been widely used for various analyses. However, it is difficult to use LC/ESI/MS for the analysis of low polar compounds, such as polycyclic aromatic hydrocarbons. It is well known that AuCl4? ion decomposes to AuCl3 by heating, and AuCl3 is a strong π‐electrophilic Lewis acid. Low polar compounds (pyrene, benzo[a]pyrene, perylene, benzo[ghi]perylene, dibenzothiophene and p‐dimethoxybenzene) were detected by ESI/MS in the positive ion mode by adding NaAuCl4. The low polar compound interacts with AuCl3 formed at the ESI interface, and undergoes electron transfer to AuCl3. The radical cation of the low polar compound was then detected by MS. In addition, the LC/ESI/MS determination of polycyclic aromatic hydrocarbons by the post‐column addition of NaAuCl4 was studied. © 2016 The Authors Journal of Mass Spectrometry Published by John Wiley & Sons Ltd 相似文献
14.
Humberto Hinojosa-GómezAuthor Vitae J. Fernando Barragán-ArocheEnrique R. Bazúa-RuedaAuthor Vitae 《Fluid Phase Equilibria》2010
In this work we present two modifications to the Peng–Robinson-Fitted equation of state where pure component parameters are regressed to vapor pressure and saturated liquid density data. The first modification (PR-f-mod) is a method that enhances the equation of state pure component property predictions through simple temperature dependent pure component parameters. In the second modification (PR-f-prop) we propose a temperature dependency for co-volume b in the repulsive parameter of the EoS, and revise the temperature function in the attractive term. The agreement with experimental data for 72 pure substances, including highly polar compounds, is remarkably good. We obtain average absolute deviations in saturated liquid density of less than 1% for all substances studied. 相似文献
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16.
Maja Karaman Ljiljana Janjušević Dragica Jakovljević Filip Šibul 《Natural product research》2019,33(10):1522-1526
This study outlines antioxidant and anti-AChE activities of the polysaccharide (PSH) extract from the mushroom species Amanita strobiliformis. Both the presence of α and ß glucans within the aforementioned extract was recorded. PSH extract displayed a profound scavenging activity of OH radicals (IC50 value, 11.86 ± 0.59 μg/mL) and high potential for reduction of Fe3+ ions (174.11 ± 8.70 mg eq. AA/g d.w.) being almost 48- and 5-fold more effective than mannitol and butylated hydroxytoluene used as a positive control, respectively. Compared with galanthamine (0.001 μg), the same extract exhibited a moderate anti-AChE activity (10 μg) in solid. Since purified PSH extract exhibited higher bioactivity (IC50 value 7.27 ± 0.31 μg/mL, 197.68 ± 9.47 mg eq. AA/g d.w. and 0.1 μg, respectively), it can be predominantly ascribed to the polysaccharide compounds. A. strobiliformis PSH extract may be considered as a promising resource of potent bioactive polysaccharides of natural origin successfully addressing both oxidative stress and lack of acetylcholine. 相似文献
17.
Emrah Gormez Ozgur Golge Miguel ngel Gonzlez-Curbelo Bulent Kabak 《Molecules (Basel, Switzerland)》2023,28(1)
Cherries are popular fruits due to their health benefits, organoleptic quality, and attractive appearance. Since highly polar pesticides are of low mass and amphoteric character, and are not amenable to traditional multi-residue extraction methods, they are more commonly not included in the pesticide monitoring program. This study aims to determine twelve highly polar pesticide residues in cherry samples intended for export from Turkey. A total of 16,022 cherry samples from 2018–2020 harvests in four production areas of Turkey were analyzed using a modification of the Quick Polar Pesticides method and liquid chromatography-tandem mass spectrometry. The method was validated at two fortification levels (0.01 and 0.05 mg kg−1), and good recoveries (87.4–111.4%) and relative standard deviations (<6%) were achieved for all analytes. The limits of quantification were in the range of 1.08–2.55 μg kg−1. Overall, 28.4% of the analyzed cherry samples were detected with phosphonic acid, calculated as fosetyl aluminium (fosetyl-Al) in amounts up to 77.7 mg kg−1. For 2304 samples (14.4%), the residues exceeded the European Union maximum residue level of 2 mg kg−1. There is no reason to be concerned about long-term exposure to phosphonic acid/fosetyl-Al, and the other highly polar pesticides through the consumption of sweet cherry. 相似文献
18.
为了分析半球谐振陀螺仪非敏感轴X、Y轴存在比力输入时,对输出角速率解算精度的影响,首先,利用环形谐振子的动力学方程,得到了径向振动方程。然后,分析了存在比力输入时,谐振子唇沿中心将偏移激励器和位移传感器所确定的圆心,并根据闭环检测原理,推导了陀螺仪解算角速率误差的表达式,仿真计算了相对偏移量对输出结果的影响程度。最后,利用分度头进行了非敏感轴的多位置翻滚试验,验证了输出中存在与非敏感轴比力输入有关的误差。 相似文献
19.
Computer simulations have been carried out to test the recently proposed model for the nanodomain structure of relaxor ferroelectrics such as lead zinc niobate (PZN). In this recent model it was supposed that the polar nanodomains are three‐dimensional, that the observed diffuse rods of scattering originate from the boundaries between domains and that the Pb displacements may be directed along , or . This is in marked contrast to a previously published model, which described the polar domains as thin plates with Pb displacements confined to the directions within the essentially two‐dimensional domains. The present results confirm that and types of Pb displacement are viable possibilities, but the number of domain boundaries required to produce sufficiently strong diffuse rods of scattering means that individual domains cannot be described as three‐dimensional and must still be relatively thin. The current work has been carried out with no direct involvement of the B‐site cation ordering, which many workers assume is necessary to understand the formation of the polar nanodomains. While it may be true that the B‐site cation distribution could provide an underlying perturbation field that might ultimately limit the extent of any polar domain, it is certainly not necessary to produce the observed scattering effects. 相似文献
20.