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1.
吐哈盆地侏罗纪煤中主要组分结构特征与生烃性分析 总被引:10,自引:0,他引:10
在高纯度煤岩显微组分分离富集的基础上,应用透射式显微傅里叶红外光谱技术 (Micro FTIR),对吐哈盆地侏罗纪煤中的主要组分-镜质体、丝质体、角质体、藻类体的结构组成进行了测定。结果表明 :藻类体主要由长链脂族结构组成,芳香结构含量相对较少;角质体和基质镜质体中含有较丰富的芳香结构以及长链脂族结构;而丝质体则主要由芳香结构组成,脂族结构含量很少。显微组分的这种结构特征决定了藻类体具有很高的生烃潜力、角质体和镜质体的生烃潜力中等、而丝质体的生烃潜力则很低。对于吐哈盆地煤成油来说,由于藻类体主要由长链脂族结构组成,并且生烃潜力也高,因此其具有高的液态烃产率、丝质体的产油率最小、角质体和镜质体的液态烃产率中等。由于镜质体是本区煤中含量最高的组分。因此,对于吐哈盆地所形成的具有工业规模的油田来说,镜质体应该是主要的贡献组分之一。但对于富含藻类体的厚层状烛藻煤,由于它类型好,品质高、生烃潜力大、以中长链脂族结构为主,是煤成油最理想的源岩。 相似文献
2.
Annealing at 400?T?600 °C (40?P?60 MPa and HM buffer-controlled f(O2)) of tourmalines synthesised at the same T and P with NNO buffer induces an oxidation of Fe2+ into Fe3+ in some Y sites only (Mössbauer Spectroscopy data). Annealing in the same conditions of natural tourmalines is consistent with these results. FTIR spectroscopy shows that oxidation of Fe2+ into Fe3+ is charge-balanced by deprotonation of the external OH(3) groups. To cite this article: Y. Fuchs et al., C. R. Geoscience 334 (2002) 245–249. 相似文献
3.
用显微荧光和显微傅立叶红外光谱研究显微组分的热演化规律 总被引:4,自引:0,他引:4
镜质体反射率是确定油源岩成熟度最广泛使用的参数,显微荧光强度及其变化也已成为检测烃源岩有机质生烃尤其是生油的标志之一,而红外光谱在研究生油母质干酪根的结构、类型和生烃潜力等方面均取得了大量的研究成果,特别是傅立叶红外显微镜的问世,给单显微组分提供了一种有效的研究手段。本文应用上述方法对一套人工熟化样品进行了检测和分析,探讨了显微组分的光性演变特征和化学成分的变化规律,并建立了显微组分的生油模式。 相似文献
4.
铜在坡缕石中的吸附位置和吸附机理研究 总被引:4,自引:0,他引:4
对四个吸附铜的坡缕石的解吸附实验研究表明,被解吸附的铜来自于坡缕石的表面和纤维状晶体的网状空隙。吸附铜的坡缕石的X射线光电子能谱(XPS)上出现了932.5eV和933.7eV的光电子峰,表明坡缕石表面的铜以Cu^+和Cu^2+的形式存在;傅立叶变换红外吸收光谱(FTIR)上八面体离子的吸收峰出现规律性偏移,其中Mg3OH和Al2□OH吸收峰向高频方向移动了3~5cm^-1,部分铜离子进入到坡缕石的晶体结构的通道中;电子顺磁共振谱上(ESR)出现了g=2.34、2.12、2.08和2.05等4个信号:表明铜离子位于H^+难以到达的位置。吸附铜的坡缕石的矿物学研究及其解吸附实验的结果均表明铜在坡缕石中以3种形式存在:①以Cu^+和Cu^2+的形式吸附在坡缕石纤维的表面,与坡缕石表面的悬空氧成键;②以ECu(H2O)4]^2+的形式存在于坡缕石的晶体结构的微空腔中(通道);③以Cu^2+的形式存在于坡缕石晶体结构中的硅氧四面体六元环的底部或八面体位。 相似文献
5.
Products and mechanisms for the gas-phase reactions of NO3 radicals with CH2=CHCl, CH2=CCl2, CHCl=CCl2,cis-CHCl=CHCl andtrans-CHCl=CHCl in air have been studied. The experiments were carried out at 295±2 K and 740±5 Torr in a 480-L Teflon-coated reaction chamber and at 295±2 K and 760±5 Torr in a 250-L stainless steel reactor. NO3 was generated by the thermal dissociation of N2O5. Experiments with15NO3 and CD2CDCl have also been performed. The initially formed nitrate peroxynitrates decay into carbonyl compounds, nitrates, HCl and ClNO2. In adidtion, there are indications of nitrooxy acid chlorides being produced. The reactions with CH2=CCl2 and CHCl=CCl2 are more complex due to release of chlorine atoms which eventually lead to formation of chloroacid chlorides.A general reaction mechanism is proposed and the observed concentration-time profiles of reactants and products are simulated for each compound. The rate constants for the initial step of NO3 addition to the chloroethenes are determined as: (2.6±0.5, 9.4±0.9, 2.0±0.4 and 1.4±0.4) × 10–16 cm3 molecule–1 s–1 for CH2=CHCl, CH2=CCl2, CHCl=CCl2 andcis-CHCl=CHCl, respectively. 相似文献
6.
The incorporation of hydrogen (deuterium) into the coesite structure was investigated at pressures from 3.1 to 7.5 GPa and
temperatures of 700, 800, and 1100 °C. Hydrogen could only be incorporated into the coesite structure at pressures greater
5.0 GPa and 1100 °C . No correlation between the concentration of trace elements such as Al and B and the hydrogen content
was observed based on ion probe analysis (1335 ± 16 H ppm and 17 ± 1 Al ppm at 7.5 GPa, 1100 °C). The FTIR spectra show three
relatively intense bands at 3575, 3516, and 3459 cm−1 (ν1 to ν3, respectively) and two very weak bands at 3296 and 3210 cm−1 (ν4 and ν5, respectively). The band at 3516 cm−1 is strongly asymmetric and can be resolved into two bands, 3528 (ν2a) and 3508 (ν2b) cm−1, with nearly identical areas. Polarized infrared absorption spectra of coesite single-crystal slabs, cut parallel to (0 1
0) and (1 0 0), were collected to locate the OH dipoles in the structure and to calibrate the IR spectroscopy for quantitative
analysis of OH in coesite (ɛ
i
,tot=190 000 ± 30 000 l mol−1
H2O cm−2). The polarized spectra revealed a strong pleochroism of the OH bands. High-pressure FTIR spectra at pressures up to 8 GPa
were performed in a diamond-anvil cell to gain further insight into incorporation mechanism of OH in coesite. The peak positions
of the ν1, ν2, and ν3 bands decrease linearly with pressure. The mode Grüneisen parameters for ν1, ν2, and ν3 are −0.074, −0.144 and −0.398, respectively. There is a linear increase of the pressure derivatives with band position which
follows the trend proposed by Hofmeister et al. (1999). The full widths at half maximum (FWHM) of the ν1, ν2, and ν3 bands increase from 35, 21, and 28 cm−1 in the spectra at ambient conditions to 71, 68, and 105 in the 8 GPa spectra, respectively. On the basis of these results,
a model for the incorporation of hydrogen in coesite was developed: the OH defects are introduced into the structure by the
substitution Si4+(Si2)+4O2−= [4]□(Si2) + 4OH−, which gives rise to four vibrations, ν1, ν2a, ν2b, and ν3. Because the OH(D)-bearing samples do contain traces of Al and B, the bands ν4 and ν5 may be coupled to Al and/or B substitution.
Received: 19 December 2000 / Accepted: 23 April 2001 相似文献
7.
傅立叶变换红外光谱联用技术在化石燃料分析中的应用 总被引:2,自引:0,他引:2
对傅立叶变换红外光谱联用技术在化石燃料分析中的应用进行了较全面的总结评述,重点介绍了气相色谱/红外光谱联机、高压液相色谱/红外光谱联机、薄层色谱/红外光谱联机、超临界流体色谱/红外光谱联机、裂解色谱/红外光谱联机、热重分析/红外光谱联机、气相色谱/红外光谱/质谱三机联用技术等在化石燃料的结构组分分析、成因机理研究及其勘探等诸方面的重要应用,尤其是在芳香族化合物和几何异构体的分离鉴定方面发挥出的突出功效。引用文献59篇。 相似文献
8.
W. Bell C. Paton Walsh P.T. Woods T.D. Gardiner M.P. Chipperfield A.M. Lee 《Journal of Atmospheric Chemistry》1998,30(1):131-140
We outline how ground-based Fourier transform infrared (FTIR) measurements of stratospheric trace species, obtained with high temporal resolution, could be used to detect filaments of polar vortex air at mid-latitudes and therefore test high spatial resolution chemical transport models (CTMs). Vertical column abundances of HCl, ClONO2, HNO3, N2O and HF have been obtained from FTIR solar absorption measurements made throughout the day from Aberdeen, UK (57°N, 2°W) on several days during winter/spring 1993/94 and 1994/95. The short-timescale ( 2 hours) variability observed in the columns is attributed to real atmospheric variations and is often associated with the passage of high latitude air over Aberdeen. This is confirmed by 3D modelling studies which qualitatively reproduce and rationalise the observed changes in the column data on January 19 1994, January 20 1995 and February 26 1995. We describe the viewing geometry of ground-based FTIR measurements and we suggest a measurement strategy which should maximise the information retrieved on horizontal gradients in stratospheric trace species columns from FTIR measurements. 相似文献
9.
10.
我国玉器市场的繁荣发展,使得玉器优劣并存,导致大量墨绿色“石材”充斥市场,充当翡翠销售.在广东玉器加工批发集散市场上收集了多种墨绿色仿翡翠原料,挑选具有代表性的4件原料进行测试分析.通过宝石显微镜观察、折射率、密度以及红外光谱、X射线粉末衍射、偏光显微镜薄片鉴定等测试方法进行对比研究.该4件样品的密度、折射率与翡翠一致,红外反射光谱与绿辉石非常相似,但其结构特征、矿物组成明显区别于翡翠.综合国标判定,该4件样品均为仿翡翠品.笔者提醒,常规宝石学测试和红外光谱测试不易区分此类制品,而加强基础性研究、提高镜下鉴定能力是防范检测风险的有效途径. 相似文献