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241.
应用红外光谱法,研究了不同pH值和Cu2+浓度条件下,合成赤铁矿和三羟铝石吸附Cu2+后表面羟基结构及其特征吸收峰的变化。结果表明:(1)随Cu2+浓度增加,赤铁矿表面H—O—H和OH的变形振动参与了吸附反应,Cu2+强烈地缔结在Fe—O上,形成了Fe—O—(Cu)结构。(2)酸性条件下,H+破坏了赤铁矿表面的O—H结构,NO3-促使弱峰1 131 cm-1的产生。随pH值增大,赤铁矿表面OH-逐渐由伸缩振动转变为变形振动,Fe—OH和Fe3+—O2-结构不断发生改变。(3)三羟铝石对Cu2+的吸附发生在高波位,随Cu2+浓度增大,其表面游离羟基的O—H弯曲振动、水分子的OH-伸缩振动和H—O—H弯曲振动均参与了吸附反应,Al—O基中的Al3+渐被Cu2+取代从而加强了较低波位的振动强度。(4)随pH值增加,三羟铝石Al—OH的弯曲振动和Al—O的伸缩振动逐渐发生着改变,表明吸附Cu2+后,在其表面形成了AlOCu+与AlOCuOH结构。 相似文献
242.
Jiaqing ZhuangZhiguo Xia Haikun LiuZepeng Zhang Libing Liao 《Applied Surface Science》2011,257(9):4350-4353
Green-emitting phosphors Ca3SiO4Cl2:Eu2+ were prepared by the high temperature solid-state method. Sol-gel process was adopted to encapsulate the as-prepared phosphors with tetraethylorthosilicate (TEOS) as silicon coating reagent. Fluorescence spectrometer, scanning electron microscopy (SEM) and powder X-ray diffraction (XRD) patterns were employed to characterize the emission spectra, the surface morphologies and the phase structures, respectively. The chemical stability testing was operated by the method of soaking the phosphors in deionized water and roasting them at different temperatures. The results indicated that the surfaces of the green phosphors were evenly coated by SiO2 and the phase structure of the coated phosphors remained the same as the uncoated samples. The luminance centre of Eu2+ did not shift after surface treatment and the luminance intensity of coated phosphors was lower than that of the uncoated samples. The results demonstrated that the water-resistance stability of the coated phosphor was improved to some degree because the pH value and the luminance intensity variation were both smaller than the uncoated phosphor after steeping within the same time. Moreover, the thermal stability of coated phosphors was enhanced obviously compared to the original samples based on the temperature dependent emission spectra measurement. 相似文献
243.
244.
S.M. Masoudpanah S.A. Seyyed Ebrahimi 《Journal of magnetism and magnetic materials》2011,323(21):2643-2647
Strontium hexaferrite SrFe12O19 thin films have been synthesized at different pH, adjusted by NH4OH, on the Si (1 0 0) substrate using a spin coating sol-gel process. Fourier transform infrared spectroscopy analysis and theoretical calculations were conducted for determination and controlling metal citrates in solution precursors. X-ray diffraction, scanning electron microscopy and vibrating sample magnetometer were applied to evaluate the composition, microstructure, crystallite size and magnetic properties of the SrFe12O19 thin films. Using the solution with pH 7, the approximately single phase strontium hexaferrite thin films with optimum physical properties can be obtained at calcination temperature of 800 °C. The SrFe12O19 thin films derived from the solution with pH 7 after calcination at 800 °C exhibited crystallite size of 42 nm and magnetic properties of Ms=267 emu/cm3 (at 10 kOe), Mr=134 emu/cm3 and Hc=4290 Oe. 相似文献
245.
《Analytical letters》2012,45(15):2305-2318
The A21978C family of compounds includes precursors of daptomycin, an important antibiotic for the treatment of diseases infected by Gram-positive resistant bacteria. Focusing on these valuable compounds, the differences in metabolites obtained with or without pH control in their producing strain Streptomyces parvus HCCB10043 were investigated by comparative metabolomics analysis based on UPLC-TOF-MS technology. According to principal component analysis, there were fourteen biomarker compounds selected under the two pH culture conditions. The ten known compounds were divided into two types: a glycoside family participating in the primary metabolism (daidzein, glycitein, genistein, and soyasaponin Bb) and a peptide family of secondary metabolites (valistatin, bestatin, 3-amino-2-hydroxy-4-phenylbutanoylvalylisoleucine, and arylomycins A2, A4, and A5). Through orthogonal partial least squares-discriminant analysis, three compounds, soyasaponin Bb and arylomycins A2 and A4 were identified as the most relevant compounds to A21978C1-3 production, the glycolytic pathway, and the NRPS synthesis pathway. The competitive relationship between arylomycin and A21978C was verified. These results have demonstrated the usefulness of the metabolomic strategy based on UPLC-MS in studying significant metabolic changes in actinomycetes. Moreover, this metabolomic strategy can provide new ideas and guidance for the regulation and improvement of secondary metabolites production. 相似文献
246.
Yukari Oda Shokyoku Kanaoka Sadahito Aoshima 《Journal of polymer science. Part A, Polymer chemistry》2010,48(5):1207-1213
For the precision synthesis of primary amino functional polymers, cationic polymerization of a phthalimide‐containing vinyl ether monomer precursor, 2‐vinyloxyethyl phthalimide (PIVE), was examined using a base‐assisting initiating system. Living polymerization of PIVE in CH2Cl2 in the presence of 1,4‐dioxane as an added base yielded nearly monodispersed polymers (Mw/Mn < 1.1) and higher molecular weight polymers, which have never been obtained using other initiating systems. Furthermore, block copolymers with hydrophobic or hydrophilic groups could be prepared. The deprotection of the pendant phthalimide groups gave well‐defined pH‐responsive polymers with pendant primary amino groups. Dual‐stimuli–responsive block copolymers having a pH‐responsive polyamine segment and a thermosensitive segment self‐assembled in water in response to both pH and temperature. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1207–1213, 2010 相似文献
247.
A proposed structure for the diffusible extracellular factor (DF) of Xanthomonas campestris pv. campestris (Xcc) has been synthesized. Its MS spectrum and biological activity, however, contradict those of the natural product previously reported, suggesting that the structure for DF of Xcc must be reexamined. 相似文献
248.
Jie Chen Jin‐Jin Li Zheng‐Hong Luo 《Journal of polymer science. Part A, Polymer chemistry》2013,51(5):1107-1117
In this work, fluorinated nonamphiphilic gradient copolymers of tert‐butyl acrylate (tBA) and 2,2,3,3,4,4,4‐heptafluorobutyl methacrylate (HFBMA) [poly(tBA‐grad‐HFBMA)] were first synthesized by semibatch atom transfer radical copolymerization of tBA and HFBMA. Their hydrolysis at acidic conditions led to amphiphilic poly(acrylic acid‐grad‐HFBMA). The chemical compositions and structures of these copolymers were characterized by proton nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy, and gel permeation chromatography. Their surface properties were evaluated with water contact angle measurement and x‐ray photoelectron spectroscopy. The micellization behaviors of amphiphilic copolymer were also studied by transmission electron microscopy and dynamic light scattering. The results showed that the fluorinated and amphiphilic gradient copolymers could self‐assemble in a dilute solution to form aggregates of morphologies. Furthermore, the effect of pH on the aggregates was investigated to verify that the resulting gradient copolymers were to some extent pH sensitive. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
249.
Y. K. Leong 《Colloid and polymer science》1999,277(4):299-305
Adsorbed polystyrene sulphonate (PSS) shifts the pH of the zero zeta potential, pHς = 0, of ZrO2 to a lower pH. The positive charge density of ZrO2 at pH = pHς=0 determined from the amount of PSS adsorbed was in excellent agreement with that obtained from charge titration. Polystyrene
sulphonic acid shifts pHς=0 to a greater degree compared with polyacrylic acid because it is a much stronger acid. A patch is likely to just consist of
one adsorbed molecule. The patch is negative when the charges of the molecule exceed the underlying positive surface charge.
Attraction between the negative patch and the bare positive surface of a second particle is responsible for increasing the
yield stress of concentrated ZrO2 dispersions at pHς=0. Its magnitude is only of the order of the van der Waals attraction. Increasing ionic strength and patch misalignment diminish
the attraction. The upper limit of the patch area was estimated from the radius of gyration of the molecule in solution. With
a known patch area, the patch charged density can be calculated. With the selection of an appropriate patch area, the yield
stress due to charged patch attraction increases linearly with the product of the negative and positive patch densities.
Received: 30 March 1998 Accepted: 18 September 1998 相似文献
250.