THE STRUCTURE OF ARTIFICIAL GRAPHITES AS REVEALED BY X-RAY, ELECTRON MICROSCOPE, AND ADSORPTION STUDIES

1957 ◽  
Vol 35 (1) ◽  
pp. 15-22 ◽  
Author(s):  
L. G. Wilson ◽  
H. L. McDermot

Three artificial graphites have been studied by X-ray, electron microscope, and adsorption techniques. Surface areas were calculated from the adsorption isotherms and from the X-ray spectra. The two sets of areas were of the same order of magnitude and varied from 18 m.2/g. for the graphite of smallest surface area to 385 m.2/g. for the graphite of largest surface area. The appearance of the graphites under the electron microscope was in qualitative agreement with the adsorption and X-ray data.

1968 ◽  
Vol 46 (10) ◽  
pp. 1695-1701 ◽  
Author(s):  
D. J. C. Yates

The determination of the surface areas of zeolites is discussed. It is shown that it is incorrect to use the multilayer isotherm method of Brunauer, Emmett, and Teller for solids where only little more than one monolayer can be adsorbed, in cavities little larger than the adsorbed molecules. The areas of such materials can, however, be determined from the beginning of the linear portion of their isotherms (point B). In addition, X-ray spectra can provide an independent method of measuring changes in the surface areas of zeolites.


Nanomaterials ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2527
Author(s):  
Tingting Niu ◽  
Bin Zhou ◽  
Zehui Zhang ◽  
Xiujie Ji ◽  
Jianming Yang ◽  
...  

Resorcinol-formaldehyde/titanium dioxide composite (RF/TiO2) gel was prepared simultaneously by acid catalysis and then dried to aerogel with supercritical fluid CO2. The carbon/titanium dioxide aerogel was obtained by carbonization and then converted to nanoporous titanium carbide/carbon composite aerogel via 800 °C magnesiothermic catalysis. Meanwhile, the evolution of the samples in different stages was characterized by X-ray diffraction (XRD), an energy-dispersive X-ray (EDX) spectrometer, a scanning electron microscope (SEM), a transmission electron microscope (TEM) and specific surface area analysis (BET). The results showed that the final product was nanoporous TiC/C composite aerogel with a low apparent density of 339.5 mg/cm3 and a high specific surface area of 459.5 m2/g. Comparing to C aerogel, it could also be considered as one type of highly potential material with efficient photothermal conversion. The idea of converting oxide–carbon composite into titanium carbide via the confining template and low-temperature magnesiothermic catalysis may provide new sight to the synthesis of novel nanoscale carbide materials.


2017 ◽  
Vol 17 (2) ◽  
pp. 129-134 ◽  
Author(s):  
Dawei Gao ◽  
Lili Wang ◽  
Chunxia Wang ◽  
Yuping Chang ◽  
Pibo Ma

Abstract Polyacrylonitrile (PAN)/Co(OAc)2/carbon nanotubes (CNTs) composite nanofibers were fabricated via electrospinning with N,N-dimethylformamide (DMF) as solvent, and by carbonization and activation of the above precursor nanofibers, porous carbon composite nanofibers were successfully obtained. Scanning electron microscope, X-ray diffraction, ASAP 2020, and Solartron 1470 were used to characterize the surface morphology, the phase composition, specific surface area, and electrochemical property of the nanofibers, respectively. The result showed that some of the fibers were broken after sintering, and the surface area and pore volume of the porous C/Cu/CNTs were 771 m2/g and 0.347 cm3/g, respectively. The specific capacitance of the composite nanofibers reached up to 210 F/g at the current density of 1.0 A/g. Its energy density and power density were 3.1 Wh/Kg and 2,337 W/Kg, respectively, at the current of 0.5 and 5 mA.


2021 ◽  
Author(s):  
Xiaodong Zhu ◽  
Qin Zhou ◽  
Yangwen Xia ◽  
Juan Wang ◽  
Hongjin Chen ◽  
...  

Abstract Pure TiO2 and different concentrations of Cu–doped TiO2 with anatase/rutile/brookite triphasic structure were successfully synthesized through a simple hydrothermal process and characterized by X–ray diffraction (XRD), Raman, scanning electron microscope (SEM), transmission electron microscope (TEM), X–ray photoelectron spectra (XPS), diffuse reflectance spectra (DRS), photoluminescence spectra (PL) and Brunauer-Emmett-Teller surface area (BET). Both pure and Cu–doped TiO2 show relatively high photocatalytic activity owing to their considerable surface areas. Moreover, the three–phase coexisting structure and the conversion between Cu2+ and Cu+ ions facilitate the separation of photogenerated electrons and holes, which is favorable for photocatalytic performance. 1%Cu–TiO2 exhibits the highest photocatalytic activity and the degradation degree of rhodamine B (RhB) reaches 93.5% after 30 min, which is higher than that of monophasic/biphasic 1%Cu–TiO2. ·O2− radical is the main active specie, and h+ and ·OH are subsidiary in the degradation process.


2011 ◽  
Vol 399-401 ◽  
pp. 1915-1918
Author(s):  
Rui Jie Guo ◽  
Xiao Juan Sha ◽  
Lei Lei Cao

The lamellar nanostructured yttrium films on α-Al2O3 substrates were successfully synthesized by electroless deposition using the lyotropic liquid crystalline templating strategy. The reaction of hydrazine hydrate and Y3+ dissolved within the aqueous domains of the lyotropic liquid crystalline phase produced the nanostructured yttrium films. The low-angle X-ray diffraction (XRD), transmission electron microscope (TEM) and scanning electron microscope (SEM) indicated that the as-resulted films possessed lamellar regular array of nanochannels with periodicity of 6 nm. With well-defined nanochannels and higher surface areas, the nanostructured films may find applications in the field of electronic materials.


2012 ◽  
Vol 616-618 ◽  
pp. 1797-1800
Author(s):  
Yu Mei Gong ◽  
Qing Liang ◽  
Jing Chuan Song ◽  
Ling Ming Xia

This paper presents the preparation of bimodal crystalline macro-/mesoporous titania powders by using a pluronic polymer (EO20PO70EO20, P123) as a template through a hydrothermal treatment. The as-prepared powders were characterized by X-ray diffraction (XRD), nitrogen adsorption-desorption, scanning electron microscope (SEM) and transmission electron microscope (TEM). The results reveal that the amount of P123 has a significant effect on the surface area of the mesoporous titania. When the mass ratio of P123:TBOT is 1:14, the crystalline macro-/mesoporous titania has the largest surface area (120.96 m2/g), the average pore diameter of this sample reaches a minimum of 6.67 nm.


1948 ◽  
Vol 26a (4) ◽  
pp. 236-242 ◽  
Author(s):  
J. C. Arnell ◽  
W. M. Barss

The surface areas, as determined from X-ray diffraction and low temperature nitrogen adsorption data, were compared for a number of carbon blacks and activated charcoals. Comparative data were also obtained on samples of charcoal at various stages of activation and after calcination. The X-ray diffraction data indicated that all the samples examined were composed of small graphitelike crystallites of the same order of magnitude, which had specific surfaces of about 2500 to 3000 sq. m. per cc. The nitrogen adsorption surface of a highly activated charcoal was found to be about equal to the X-ray surface. It is suggested that the crystallite surface represents the potential adsorption surface of a carbonaceous material and, providing that crystal growth does not occur during activation, the activation process makes these surfaces available to external adsorbate.


Geochronology ◽  
2019 ◽  
Vol 1 (1) ◽  
pp. 17-41 ◽  
Author(s):  
Emily H. G. Cooperdock ◽  
Richard A. Ketcham ◽  
Daniel F. Stockli

Abstract. (U–Th) ∕ He thermochronometry relies on the accurate and precise quantification of individual grain volume and surface area, which are used to calculate mass, alpha ejection (FT) correction, equivalent sphere radius (ESR), and ultimately isotope concentrations and age. The vast majority of studies use 2-D or 3-D microscope dimension measurements and an idealized grain shape to calculate these parameters, and a long-standing question is how much uncertainty these assumptions contribute to observed intra-sample age dispersion and accuracy. Here we compare the results for volume, surface area, grain mass, ESR, and FT correction derived from 2-D microscope and 3-D X-ray computed tomography (CT) length and width data for > 100 apatite grains. We analyzed apatite grains from two samples that exhibited a variety of crystal habits, some with inclusions. We also present 83 new apatite (U–Th) ∕ He ages to assess the influence of 2-D versus 3-D FT correction on sample age precision and effective uranium (eU). The data illustrate that the 2-D approach systematically overestimates grain volumes and surface areas by 20 %–25 %, impacting the estimates for mass, eU, and ESR – important parameters with implications for interpreting age scatter and inverse modeling. FT factors calculated from 2-D and 3-D measurements differ by ∼2 %. This variation, however, has effectively no impact on reducing intra-sample age reproducibility, even on small aliquot samples (e.g., four grains). We also present a grain-mounting procedure for X-ray CT scanning that can allow hundreds of grains to be scanned in a single session and new software capabilities for 3-D FT and FT-based ESR calculations that are robust for relatively low-resolution CT data, which together enable efficient and cost-effective CT-based characterization.


Clay Minerals ◽  
1978 ◽  
Vol 13 (4) ◽  
pp. 375-385 ◽  
Author(s):  
A. Jiménez-López ◽  
J. de D. López-González ◽  
A. Ramīrez-Sāenz ◽  
F. Rodrīguez-Reinoso ◽  
C. Valenzuela-Calahorro ◽  
...  

AbstractThe variations in surface area of a sepiolite (Toledo, Spain) after acid and heat treatments (1 n to 5 n, HNO3, 110°C to 900°C for 100 h) have been studied. Surface areas have been determined from N2 adsorption isotherms at 77 K using B.E.T., Langmuir and Dubinin-Radushkevich equations. SBET values range from 65 up to 391 m2 g−1, the maximum value corresponding to the sample activated with 1 n HNO3 solution and treated at 300°C. SL and SD-R values are similar, but slightly larger than the corresponding SBET values.A correlated study has been carried out with samples activated with 1 n and 2 n HNO3 solutions and heat treated at 110, 200, 300, 400 and 500°C for 10 h. SBET values of these samples are rather similar to those of the corresponding samples treated during 100 h.


2019 ◽  
Author(s):  
Emily H. G. Cooperdock ◽  
Richard A. Ketcham ◽  
Daniel F. Stockli

Abstract. (U-Th)/He thermochronometry relies on accurate and precise quantification of individual grain volume and surface area, which are used to calculate mass, alpha ejection (FT) correction, isotope concentrations, equivalent sphere radius (ESR), and ultimately age. The vast majority of studies use 2D or 3D microscope dimension measurements and an idealized grain shape to calculate these parameters, and a long-standing question is how much uncertainty these assumptions contribute to observed intra-sample age dispersion and accuracy. Here we compare the results for volume, surface area, grain mass, ESR, effective uranium (eU) and FT correction derived from 2D microscope and 3D x-ray computed tomography (CT) length and width data for > 100 apatite grains. We analyzed apatite grains from two samples that exhibited a variety of crystal habits, some with inclusions. We also present 83 new apatite (U-Th)/He ages to assess the influence of 2D versus 3D FT correction on sample age precision. The data illustrate that the 2D approach systematically overestimates grain volumes and surface areas by 20–25 %, impacting the estimates for mass, eU, and ESR – all important parameters used for interpreting age scatter and inverse modeling. FT factors calculated from 2D and 3D measurements differ by ~ 2 %. This variation, however, has effectively no impact on reducing intra-sample age reproducibility. We also present a grain mounting procedure for x-ray CT scanning that can allow 100's of grains to be scanned in a single session, and new software capabilities for 3D FT and FT-based ESR calculations that are robust for relatively low-resolution CT data, that together enable efficient and cost-effective CT-based characterization.


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