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101.
Silane grafted montmorillonites were synthesized by using 3-aminopropyltriethoxysilane and trimethylchlorosilane via two different grafting reaction systems: (a) ethanol-water mixture and (b) vapor of silane. The resulting products were investigated using Fourier transform infrared (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA). XRD patterns demonstrate that silane was intercalated into the montmorillonite gallery, as indicated by the increase of the basal spacing. The product prepared by vapor deposition has a larger basal spacing than that obtained from solution, due to the different extent of silane hydrolysis in various grafting systems. TGA curves indicate that the methyl groups penetrate into the siloxane clay are the primary reason for the decrease of the dehydroxylation temperature of the grafted products. 3-Aminopropyltriethoxysilane in the grafted montmorillonite adopts a bilayer arrangement while trimethylchlorosilane adopts a monolayer arrangement within the clay gallery. 相似文献
102.
Water purification is of extreme importance worldwide. p-Nitrophenol was used as a test chemical to design and test an organoclay for the removal of p-nitrophenol from an aqueous solution. Synthesis of the organoclay with methyltrioctadecylammonium bromide [CH(3)(CH(2))(17)](3)NBr(CH(3)) labeled as MTOAB results in multiple expansions of the montmorillonite clay from 1.24 nm to a maximum of 5.20 nm as is evidenced by the XRD patterns. Thermal analysis shows strong bonding of the surfactant to the clay siloxane layers and the interaction of the p-nitrophenol with the clay surfaces. It is proposed that the p-nitrophenol penetrates the siloxane layer of the clay and bonds through the ditrigonal space of the siloxane hexagonal units to the inner OH units. Such a concept is supported by the observation of an additional infrared band at 3652 cm(-1) for the organoclay. Shifts in the p-nitrophenol OH stretching vibrations mean a strong interaction of the p-nitrophenol molecule. Significant changes in the siloxane stretching bands are also observed. 相似文献
103.
Surfaces of a Wyoming SWy-2 sodium montmorillonite were modified using microwave radiation through intercalation with the cationic surfactants octadecyl-trimethyl ammonium bromide, dimethyldioctadecylammonium bromide, and methyl-tri-octadecyl ammonium bromide by an ion exchange mechanism. Changes in the surfaces and structure were characterized using X-ray diffraction (XRD), thermal analysis (TG) and infrared (IR) spectroscopy. Different configurations of surfactants within montmorillonite interlayer are proposed based on d(001) basal spacings. A range of surfactant molecular environments within the surface-modified montmorillonite are proposed based upon their thermal decomposition. IR spectroscopy using a smart endurance single bounce diamond attenuated total reflection (ATR) cell has been used to study the changes in the spectra of CH asymmetric and symmetric stretching modes of the surfactants to provide more information of the surfactant molecular configurations. 相似文献
104.
105.
Nanomaterials based upon silylated layered double hydroxides 总被引:1,自引:0,他引:1
A class of nanomaterials based upon the surface modification of layered double hydroxides (LDHs) have been synthesized by grafting silanes onto the surfaces of the LDH. By in situ coprecipitation, the surfaces of a LDH have been modified through grafting of 3-aminopropyltriethoxysilane (APTS) using the anionic surfactant Na-dodecylsulfonate (SDS). The synthesized nanomaterials were characterized by X-ray diffraction (XRD), attenuated total reflection Fourier-transform infrared spectroscopy (ATR FTIR), thermogravimetry (TG) and transmission electron microscopy (TEM). The grafted LDH (LDH-G) displays distinct XRD patterns proving the obtained materials are a new and different phase. The FTIR spectra of the silylated hydrotalcite show bands attributed to Si-O-M (M = Mg and Al) vibration at 996 cm−1, suggesting that APTS has successfully been grafted onto the LDH layers. The TG curves prove the grafted sample has less M-OH concentration and less interlayer water molecules, as indicated by the M-OH consumption during the condensation reaction between Si-OH and M-OH on the LDH surface. The grafted sample displays a ribbon-like thin sheet in the TEM images, with the lateral thickness estimated as 2.5 nm. 相似文献
106.
The uranyl tellurite mineral moctezumite, Pb(UO2)(TeO3)2, was studied by Raman spectroscopy and complemented with infrared spectroscopy. The presence of the stretching and bending vibrations of uranyl (UO2)2+ and tellurite (TeO3)2− ions was inferred, and the observed bands were assigned to uranyl and tellurite units vibrations. U O bond lengths calculated from the spectra with two empirical relations are close to those inferred from the X‐ray single‐crystal structure of moctezumite. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
107.
Tellurites may be subdivided according to formula and structure. There are five groups based upon the formulae (a) A(XO3), (b) A(XO3)·xH2O, (c) A2(XO3)3·xH2O, (d) A2(X2O5) and (e) A(X3O8). Raman spectroscopy has been used to study the tellurite minerals teineite and graemite; both contain water as an essential element of their stability. The tellurite ion should show a maximum of six bands. The free tellurite ion will have C3v symmetry and four modes, 2A1 and 2 E. Raman bands for teineite at 739 and 778 cm−1 and for graemite at 768 and 793 cm−1 are assigned to the ν1 (TeO3)2− symmetric stretching mode while bands at 667 and 701 cm−1 for teineite and 676 and 708 cm−1 for graemite are attributed to the ν3 (TeO3)2− antisymmetric stretching mode. The intense Raman band at 509 cm−1 for both teineite and graemite is assigned to the water librational mode. Raman bands for teineite at 318 and 347 cm−1 are assigned to the (TeO3)2−ν2(A1) bending mode and the two bands for teineite at 384 and 458 cm−1 may be assigned to the (TeO3)2−ν4(E) bending mode. Prominent Raman bands, observed at 2286, 2854, 3040 and 3495 cm−1, are attributed to OH stretching vibrations. The values for these OH stretching vibrations provide hydrogen bond distances of 2.550(6) Å (2341 cm−1), 2.610(3) Å (2796 cm−1) and 2.623(2) Å (2870 cm−1) which are comparatively short for secondary minerals. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
108.
Two hydrated hydroxy magnesium carbonate minerals brugnatellite and coalingite with a hydrotalcite‐like structure were studied by Raman spectroscopy. Intense bands are observed at 1094 cm−1 for brugnatellite and at 1093 cm−1 for coalingite attributed to the CO32−ν1 symmetric stretching mode. Additional low intensity bands are observed at 1064 cm−1. The existence of two symmetric stretching modes is accounted for in terms of different anion structural arrangements. Very low intensity bands at 1377 and 1451 cm−1 are observed for brugnatellite, and the Raman spectrum of coalingite displays two bands at 1420 and 1465 cm−1 attributed to the (CO3)2−ν3 antisymmetric stretching modes. Very low intensity bands at 792 cm−1 for brugnatellite and 797 cm−1 for coalingite are assigned to the CO32− out‐of‐plane bend (ν2). X‐ray diffraction studies by other researchers have shown that these minerals are disordered. This is reflected in the difficulty of obtaining Raman spectra of reasonable quality and explains why the Raman spectra of these minerals have not been previously or sufficiently described. A comparison is made with the Raman spectra of other hydrated magnesium carbonate minerals. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
109.
The mineral xocomecatlite is a hydroxy metatellurate mineral with Te6+ O4 units. Tellurates may be subdivided according to their formula into three types of tellurate minerals: type (a) (AB)m (TeO4)pZq, type (b) (AB)m(TeO6)·xH2O and (c) compound tellurates in which a second anion including the tellurite anion, is involved. The mineral xocomecatlite is an example of the first type. Raman bands for xocomecatlite at 710, 763 and 796 cm−1, and 600 and 680 cm−1 are attributed to the ν1(TeO4)2− symmetric and ν3 antisymmetric stretching mode. Raman bands observed at 2867 and 2926 cm−1 are assigned to TeOH stretching vibrations and enable estimation of the hydrogen bond distances of 2.622 Å (2867 cm−1), 2.634 Å (2926 cm−1) involving these OH units. The hydrogen bond distances are very short implying that they are necessary for the stability of the mineral. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
110.
Sara J. Palmer Ray L. Frost Henry J. Spratt 《Journal of Raman spectroscopy : JRS》2009,40(9):1138-1143
Hydrotalcites of formula Mg6(Al,Fe)2(OH)16(CO3)·4H2O formed by intercalation with the carbonate anion as a function of divalent/trivalent cationic ratio have been successfully synthesised. The XRD patterns show variation in the d‐spacing attributed to the size of the cation. Raman and infrared bands in the OH stretching region are assigned to (1) brucite layer OH stretching vibrations, (2) water stretching bands and (3) water strongly hydrogen bonded to the carbonate anion. Multiple (CO3)2− symmetric stretching bands suggest that different types of (CO3)2− exist in the hydrotalcite interlayer. Increasing the cation ratio (Mg/Al,Fe) resulted in an increase in the combined intensity of the two Raman bands at around 3600 cm−1, attributed to Mg OH stretching modes, and a shift of the overall band profile to higher wavenumbers. These observations are believed to be a result of the increase in magnesium in the structure. Raman spectroscopy shows a reduction in the symmetry of the carbonate, leading to the conclusion that the anions are bonded to the brucite‐like hydroxyl surface and to the water in the interlayer. Water bending modes are identified in the infrared spectra at positions greater than 1630 cm−1, indicating that water is strongly hydrogen bonded to both interlayer anions and the brucite‐like surface. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献