PERMEABILITY STUDIES: II. SURFACE AREA MEASUREMENTS OF INORGANIC PIGMENT POWDERS

1947 ◽  
Vol 25a (4) ◽  
pp. 191-209 ◽  
Author(s):  
J. C. Arnell
Keyword(s):  
Experimental Data ◽  
Electron Microscope ◽  
Specific Surface ◽  
Surface Area ◽  
Satisfactory Agreement ◽  
Surface Measurement ◽  
Inorganic Pigments ◽  
Inorganic Pigment ◽  
Permeability Studies

The modified Kozeny equation has been found to be satisfactory for the measurement of the specific surface of inorganic pigments having particle diameters of the order of 0.1 to 0.2 µ to within ±10%. These powders were too fine for visual microscope counting or standard sedimentation methods of specific surface measurement. The results obtained from experimental data were checked against those calculated from electron microscope counting for two of the powders studied and found to be in satisfactory agreement.

PERMEABILITY STUDIES: III. SURFACE AREA MEASUREMENTS OF CARBON BLACKS

1948 ◽  
Vol 26a (2) ◽  
pp. 29-38 ◽  
Author(s):  
J. C. Arnell ◽  
G. O. Henneberry
Keyword(s):  
Electron Microscope ◽  
Low Temperature ◽  
Carbon Black ◽  
Surface Area ◽  
Satisfactory Agreement ◽  
Nitrogen Adsorption ◽  
Average Particle ◽  
Carbon Blacks ◽  
Permeability Studies ◽  
Nitrogen Adsorption Isotherms

The modified Kozeny equation has been found to be satisfactory for the measurement of the specific surfaces of carbon blacks having average particle diameters ranging from 0.01 to 0.1 μ to within ±10%. Comparative data were obtained from electron microscope counting and from low temperature nitrogen adsorption isotherms. The three methods examined gave results that were in satisfactory agreement, except when the carbon black was porous, and then the adsorption value was extremely large.

scholarly journals Activated Carbons from Thermoplastic Precursors and Their Energy Storage Applications

Nanomaterials ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 896 ◽  
Author(s):  
Hye-Min Lee ◽  
Kwan-Woo Kim ◽  
Young-Kwon Park ◽  
Kay-Hyeok An ◽  
Soo-Jin Park ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Specific Surface ◽  
Surface Area ◽  
Field Emission ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Activated Carbons ◽  
Total Pore Volume ◽  
Cross Linking ◽  
Mesopore Volume

In this study, low-density polyethylene (LDPE)-derived activated carbons (PE-AC) were prepared as electrode materials for an electric double-layer capacitor (EDLC) by techniques of cross-linking, carbonization, and subsequent activation under various conditions. The surface morphologies and structural characteristics of the PE-AC were observed by field-emission scanning electron microscope, Cs-corrected field-emission transmission electron microscope, and X-ray diffraction analysis, respectively. The nitrogen adsorption isotherm-desorption characteristics were confirmed by Brunauer–Emmett–Teller, nonlocal density functional theory, and Barrett–Joyner–Halenda equations at 77 K. The results showed that the specific surface area and total pore volume of the activated samples increased with increasing the activation time. The specific surface area, the total pore volume, and mesopore volume of the PE-AC were found to be increased finally to 1600 m2/g, 0.86 cm3/g, and 0.3 cm3/g, respectively. The PE-AC also exhibited a high mesopore volume ratio of 35%. This mesopore-rich characteristic of the activated carbon from the LDPE is considered to be originated from the cross-linking density and crystallinity of precursor polymer. The high specific surface area and mesopore volume of the PE-AC led to their excellent performance as EDLC electrodes, including a specific capacitance of 112 F/g.

scholarly journals Low-Temperature Synthesis of Monolithic Titanium Carbide/Carbon Composite Aerogel

Nanomaterials ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2527
Author(s):  
Tingting Niu ◽  
Bin Zhou ◽  
Zehui Zhang ◽  
Xiujie Ji ◽  
Jianming Yang ◽  
...  
Keyword(s):  
Titanium Dioxide ◽  
Electron Microscope ◽  
Low Temperature ◽  
Titanium Carbide ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Composite ◽  
Composite Aerogel ◽  
X Ray

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.

Mineralogy of the <2 μm fraction of three mixed-layer clays from southern and central Tunisia

Clay Minerals ◽  
2000 ◽  
Vol 35 (2) ◽  
pp. 375-381 ◽  
Author(s):  
H. Ben Rhaiem ◽  
D. Tessier ◽  
A. Ben Haj Amara
Keyword(s):  
Quantitative Analysis ◽  
Specific Surface ◽  
Surface Area ◽  
Clay Minerals ◽  
Chemical Method ◽  
Surface Measurement ◽  
Chemical Characteristics ◽  
Central Tunisia ◽  
Physico Chemical ◽  
Dominant Phase

AbstractThree clay minerals from southern and central Tunisia were characterized. Both XRD quantitative analysis and a chemical method were used to determine the mineralogical and physico-chemical characteristics of the <2 μm clay fractions. The XRD, CEC and specific surface measurement analyses showed that the dominant phase in all samples is illite-smectite with kaolinite and traces of quartz also present. From quantitative XRD, the abundances of the minerals identified are consistent with the measured CEC, specific surface area and TG/DTA properties. Analysis by XRD also showed that the illite-smectite phases are composed of thin stacks (two to a maximum of ten layers per stack) of random illite-smectite and ordered (R1) illite-smectite. There is also some discrete illite.

scholarly journals A Type of MOF-Derived Porous Carbon with Low Cost as an Efficient Catalyst for Phenol Hydroxylation

2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Renjie Zhou ◽  
Gui Chen ◽  
Yuejun Ouyang ◽  
Hairui Ni ◽  
Nonglin Zhou ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Porous Carbon ◽  
Physical Adsorption ◽  
Low Cost ◽  
High Specific Surface Area ◽  
Phenol Hydroxylation ◽  
Efficient Catalyst

Using MOF-5 as a template, the porous carbon (MDPC-600) possessing high specific surface area was obtained after carbonization and acid washing. After MDPC-600 was loaded with Cu ions, the catalyst Cu/MDPC-600 was acquired by heat treatment under nitrogen atmosphere. The catalyst was characterized by X-ray powder diffraction (XRD), N2 physical adsorption (BET), field emission electron microscope (SEM), energy spectrum, and transmission electron microscope (TEM). The results show that the Cu/MDPC-600 catalyst prepared by using MOF-5 as the template has a very high specific surface area, and Cu is uniformly supported on the carrier. The catalytic hydrogen peroxide oxidation reaction of phenol hydroxylation was investigated and exhibits better catalytic activity and stability in the phenol hydroxylation reaction. The catalytic effect was best when the reaction temperature was 80°C, the reaction time was 2 h, and the amount of catalyst was 0.05 g. The conversion rate of phenol was 47.6%; the yield and selectivity of catechol were 37.8% and 79.4%, respectively. The activity of the catalyst changes little after three cycles of use.

Fabrication of Activated Carbon Fibers from Stabilized PAN-Based Fibers by KOH

2004 ◽  
Vol 449-452 ◽  
pp. 217-220 ◽  
Author(s):  
Young Jae Lee ◽  
Jae Hyung Kim ◽  
Jang Soon Kim ◽  
Dong Bok Lee ◽  
Jae Chun Lee ◽  
...  
Keyword(s):  
Experimental Data ◽  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Fibers ◽  
Potassium Hydroxide ◽  
Chemical Activation ◽  
Activated Carbon Fibers ◽  
High Concentration

Activated carbon fibers were prepared from stabilized PAN-based fibers by chemical activation using potassium hydroxide at different concentration. The experimental data showed variations in specific surface area, microstructure by the activated carbon fibers. Specific surface area of about 2545 m2/g was obtained in the KOH/stabilized PAN-based fiber ratio of 1:1 at 800°. An abrupt reduction of specific surface area was observed in the experiments with the ratio of 3:1 of OH/stabilized PAN-based fiber, being dissimilar with the result of KOH/fiber ratios of 1:1 and 2:1 in the similar experiments. The high concentration of KOH led to the destruction of micropore walls instead of forming mesopores.

scholarly journals The Effect of Fly Ash on Some Surface Characteristics and Microstructure of β-C2S

1997 ◽  
Vol 15 (6) ◽  
pp. 407-417
Author(s):  
Kh.A. Khalil ◽  
A.A. Amer
Keyword(s):  
Electron Microscope ◽  
Fly Ash ◽  
Scanning Electron Microscope ◽  
Specific Surface ◽  
Surface Area ◽  
Nitrogen Adsorption ◽  
Surface Characteristics ◽  
Ash Content ◽  
Sem Investigation ◽  
Scanning Electron

The effect of the addition of fly ash (0–15 wt. %) on the surface characteristics of β-C2S and its microstructure was investigated using nitrogen adsorption at −196°C together with scanning electron microscope (SEM) techniques. The results obtained revealed that the addition of fly ash up to 5 wt. % increased the specific surface area by 32% followed by a decrease of 34% when the fly ash content was increased up to 15 wt. %. SEM investigation showed that the hydrates produced form an outer shell which coats the fly ash particles.

Mechanisms on formation of hierarchically porous carbon and its adsorption behaviors

2016 ◽  
Vol 74 (1) ◽  
pp. 266-275 ◽  
Author(s):  
Jie Liu ◽  
Lingxia Hao ◽  
Wenzhen Qian ◽  
Yu-Feng He ◽  
Rong-Min Wang
Keyword(s):  
Activated Carbon ◽  
Electron Microscope ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Photoelectron Spectroscopy ◽  
Thermo Gravimetric Analysis ◽  
Gravimetric Analysis ◽  
Hierarchically Porous ◽  
Adsorption Behaviors

Using simple one-step carbonization-activation, the residues of paulownia flowers are employed as a precursor to prepare hierarchically porous activated carbon. After investigating the optimum conditions, the obtained paulownia flowers based activated carbon (PFAC) is characterized by Fourier transform infrared spectroscopy, scanning electron microscope, transmission electron microscope, Brunauer–Emmett–Teller specific surface area analysis (SBET), thermo gravimetric analysis, and X-ray photoelectron spectroscopy. The PFAC owns a high specific surface area of 1,053 m2/g as well as a hierarchically porous structure with a combination of micro-, meso- and macropores. The pore-forming mechanism is discussed according to results of characterization. Using methylene blue as model dye, the adsorption behaviors of PFAC were investigated. We found that the dye could be rapidly adsorbed by hierarchically porous PFAC, and the adsorption capacity of PFAC reached 300 mg/g.

scholarly journals Measuring the specific surface area of mesoporous silica using x-ray scattering

2014 ◽  
Vol 70 (a1) ◽  
pp. C599-C599
Author(s):  
Julien Cambedouzou ◽  
Olivier Diat
Keyword(s):  
Experimental Data ◽  
Specific Surface ◽  
Surface Area ◽  
Mesoporous Materials ◽  
Specific Surface Area ◽  
Small Angle ◽  
X Ray ◽  
X Ray Scattering ◽  
Mcm 41 ◽  
Ray Scattering

The development of porous silica or carbon material with high specific surface area raises a high interest in the field of materials science given their potential interest in a wide range of applications including catalysis, water treatment or drug delivery. Among these mesoporous structures, those consisting of one-dimensional pores aligned along a compact hexagonal packing are of prime importance and can be referred to as "hexagonal mesoporous materials" (HMPM). The most famous silica structures of this kind are MCM-41 and SBA-15. The same symmetry can be found in carbon mesoporous materials, for example in FDU-15 structures. The precise characterization of HMPM is necessary for most of the applications envisioned for these materials (pore size, pore density, specific surface and sometimes thickness of the functionalization layer). Small angle X-ray scattering techniques offer the opportunity to determine the mean structural parameters of HMPM. Although different approaches can be found in the literature in order to numerically reproduce the experimental data obtained on HMPM or hexagonal liquid crystals, when the sample is a powder, fitting the experimental data in absolute scale with numerical models becomes necessary. However, with a large scattering contribution of grain at low q vector as well as short range correlation contribution at large q, the analysis is not so simple. In this paper, we propose a comprehensive study [1] devoted to the quantitative interpretation of small-angle scattering patterns of HMPM in terms of structure and specific surface estimation based on the formalism proposed by Spalla et al. [2]. In the case of two real samples, namely a SBA-15 and a MCM-41 powder, the specific surface area of the mesopores is estimated and is discussed in the light of gas adsorption measurements.

Changes in the Structure of Steel during Quenching in a Magnetic Field

2020 ◽  
Vol 989 ◽  
pp. 79-84 ◽  
Author(s):  
Viktor N. Pustovoit ◽  
Yuri V. Dolgachev ◽  
L.P. Aref'eva
Keyword(s):  
Magnetic Field ◽  
Experimental Data ◽  
Martensitic Transformation ◽  
Specific Surface ◽  
Surface Area ◽  
Constant Magnetic Field ◽  
Surface Relief ◽  
Volumetric Strain ◽  
Transformation Products ◽  
Electron Microscopes

The structure of martensite obtained by quenching steel under the action of a constant magnetic field was studied. The kinetic changes of the martensitic transformation, caused by the action of a magnetic field, are expressed in the structure by an increase in the dispersity of the transformation products. Samples of steels C45, 100CrMn6 and 30HGSA were investigated. Dispersity was evaluated statistically in images obtained on light and electron microscopes. The specific surface area was measured and the parameters of the surface relief caused by martensitic transformation were studied. Experimental data show that after quenching in a magnetic field, a decrease in the volumetric strain of the transformation, an increase in the dispersity of packets of martensitic crystals and components of the packets are observed. It is concluded that an increase in dispersion and a fragmentation of the structure of martensite are mainly the result of multiplicative nucleation.

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