scholarly journals Comparison of the Biological and Chemical Synthesis of Schwertmannite at a Consistent Fe2+ Oxidation Efficiency and the Effect of Extracellular Polymeric Substances of Acidithiobacillus ferrooxidans on Biomineralization

Materials ◽  
2018 ◽  
Vol 11 (9) ◽  
pp. 1739 ◽  
Author(s):  
Yongwei Song ◽  
Yelin Liu ◽  
Heru Wang
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Acidithiobacillus Ferrooxidans ◽  
Extracellular Polymeric Substances ◽  
Shell Shape ◽  
X Ray ◽  
Removal Capacity ◽  
The Difference ◽  
Oxidation Efficiency

Schwertmannite is an environmental mineral material that can promote the natural passivation of heavy metal elements, thereby reducing environmental pollution from toxic elements. However, the fundamental reason for the difference between the chemically (H2O2-FeSO4) and biologically (Acidithiobacillus ferrooxidans-FeSO4) synthesized schwertmannite is still unclear. In this study, X-ray diffraction, scanning electron microscopy, the Brunauer–Emmett–Teller method, and X-ray fluorescence spectrometry were used to compare the structure, specific surface area, and elemental composition of schwertmannite synthesized by biological and chemical methods. The removal capacity of As(III) by the two kinds of schwertmannite and the effects of extracellular polymeric substances (EPS) on biogenetic schwertmannite were also investigated. At a consistent Fe2+ oxidation efficiency, the chemical method synthesized more schwertmannite than the biological method over a 60-h period. The biosynthesized schwertmannite had a “chestnut shell” shape, with a larger particle size and specific surface than the chemically synthesized schwertmannite, which was relatively smooth. The saturated adsorption capacities of the biologically and chemically synthesized schwertmannite were 117.0 and 87.0 mg·g−1, respectively. After exfoliation of the EPS from A. ferrooxidans, the biosynthesized schwertmannite displayed a “wool ball” shape, with rough particle surfaces, many microporous structures, and a larger specific surface area. The schwertmannite yield also increased by about 45% compared with that before exfoliation, suggesting that the secretion of EPS by A. ferrooxidans can inhibit the formation of schwertmannite.

Adsorbents obtained from black liquor residues: synthesis, characterization, and evaluation in the removal of textile dyes

2021 ◽  
Vol 16 (12) ◽  
Author(s):  
Mayara Oliveira ◽  
Vinícius Gonçalves Santos ◽  
Luciene Santos Carvalho ◽  
Doris Ruiz ◽  
Igor Antunes Silva Barbosa ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Paper Industry ◽  
Black Liquor ◽  
Nitrogen Atmosphere ◽  
Blue Dye ◽  
X Ray ◽  
Removal Capacity ◽  
Different Temperatures

In this work, charcoal-type adsorbents were prepared from black liquor, a cellulose and paper industry residue rich in lignin and containing inorganic salts. During the preparation of adsorbent materials, black liquor was dried at 120 °C and then pyrolyzed at different temperatures (600 °C, 700 °C, and 800 °C) under a nitrogen atmosphere. The samples were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TG), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), measurement of specific surface area (BET), point of zero charges (PZC) determination, and evaluating of removal capacity of methylene blue dye. DRX results indicated the presence of crystalline phases of different salts, mainly sodium carbonate, on the surface of the produced carbonaceous materials from black liquor waste. Besides, a significant effect of the pyrolysis temperature on the charcoal crystallinity was observed. Materials presented low values of porosity and specific surface area, and similar morphologies. Solids' surface character was predominantly alkaline, according to PZC curves. All solids were efficient in removing 70 to 85% of the methylene blue's color.

scholarly journals Effects of Hydraulic Gradient and Clay Type on Permeability of Clay Mineral Materials

Minerals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1064
Author(s):  
Masanori Kohno
Keyword(s):  
Hydraulic Conductivity ◽  
Specific Surface ◽  
Surface Area ◽  
Clay Mineral ◽  
Specific Surface Area ◽  
Hydraulic Gradient ◽  
Consistency Index ◽  
Hydrogen Energy ◽  
The Difference ◽  
Mineral Type

Considering the relevance of clay mineral-bearing geomaterials in landslide/mass movement hazard assessment, various engineering projects for resource development, and stability evaluation of underground space utilization, it is important to understand the permeability of these clay mineral-based geomaterials. However, only a few quantitative data have been reported to date regarding the effects of the clay mineral type and hydraulic gradient on the permeability of clay mineral materials. This study was conducted to investigate the permeability of clay mineral materials based on the clay mineral type, under different hydraulic gradient conditions, through a constant-pressure permeability test. Comparative tests have revealed that the difference in the types of clay mineral influences the swelling pressure and hydraulic conductivity. In addition, it has been found that the difference in water pressure (hydraulic gradient) affects the hydraulic conductivity of clay mineral materials. The hydraulic conductivity has been found to be closely associated with the specific surface area of the clay mineral material. Furthermore, the hydraulic conductivity value measured is almost consistent with the value calculated theoretically using the Kozeny–Carman equation. Moreover, the hydraulic conductivity is also found to be closely associated with the hydrogen energy, calculated from the consistency index of clay. This result suggests that the hydraulic conductivity of clay mineral materials can be estimated based on the specific surface area and void ratio, or consistency index of clay.

scholarly journals Structural and Morphological Quantitative 3D Characterisation of Ammonium Nitrate Prills by X-Ray Computed Tomography

Materials ◽  
2020 ◽  
Vol 13 (5) ◽  
pp. 1230
Author(s):  
Fabien Léonard ◽  
Zhen Zhang ◽  
Holger Krebs ◽  
Giovanni Bruno
Keyword(s):  
Computed Tomography ◽  
Specific Surface ◽  
Ammonium Nitrate ◽  
Surface Area ◽  
Specific Surface Area ◽  
Volume Fraction ◽  
Fuel Oil ◽  
X Ray ◽  
Oil Retention ◽  
X Ray Computed

The mixture of ammonium nitrate (AN) prills and fuel oil (FO), usually referred to as ANFO, is extensively used in the mining industry as a bulk explosive. One of the major performance predictors of ANFO mixtures is the fuel oil retention, which is itself governed by the complex pore structure of the AN prills. In this study, we present how X-ray computed tomography (XCT), and the associated advanced data processing workflow, can be used to fully characterise the structure and morphology of AN prills. We show that structural parameters such as volume fraction of the different phases and morphological parameters such as specific surface area and shape factor can be reliably extracted from the XCT data, and that there is a good agreement with the measured oil retention values. Importantly, oil retention measurements (qualifying the efficiency of ANFO as explosives) correlate well with the specific surface area determined by XCT. XCT can therefore be employed non-destructively; it can accurately evaluate and characterise porosity in ammonium nitrate prills, and even predict their efficiency.

scholarly journals Preparation of Zirconia Nanofibers by Electrospinning and Calcination with Zirconium Acetylacetonate as Precursor

Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 1067 ◽  
Author(s):  
Vyacheslav V. Rodaev ◽  
Svetlana S. Razlivalova ◽  
Andrey O. Zhigachev ◽  
Vladimir M. Vasyukov ◽  
Yuri I. Golovin
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Heterogeneous Catalysts ◽  
Tetragonal Zirconia ◽  
Nitrogen Adsorption ◽  
Average Diameter ◽  
High Specific Surface Area ◽  
X Ray ◽  
Adsorption Analysis

For the first time, zirconia nanofibers with an average diameter of about 75 nm have been fabricated by calcination of electrospun zirconium acetylacetonate/polyacrylonitrile fibers in the range of 500–1100 °C. Composite and ceramic filaments have been characterized by scanning electron microscopy, thermogravimetric analysis, nitrogen adsorption analysis, energy-dispersive X-ray spectroscopy, and X-ray diffractometry. The stages of the transition of zirconium acetylacetonate to zirconia have been revealed. It has been found out that a rise in calcination temperature from 500 to 1100 °C induces transformation of mesoporous tetragonal zirconia nanofibers with a high specific surface area (102.3 m2/g) to non-porous monoclinic zirconia nanofibers of almost the same diameter with a low value of specific surface area (8.3 m2/g). The tetragonal zirconia nanofibers with high specific surface area prepared at 500 °C can be considered, for instance, as promising supports for heterogeneous catalysts, enhancing their activity.

Effects of Carbonation on the Specific Surface BET of Cement Mortar Measured by Two Different Methods: Nitrogen Adsorption and Water Adsorption

2014 ◽  
Vol 931-932 ◽  
pp. 421-425 ◽  
Author(s):  
Son Tung Pham ◽  
William Prince
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Water Adsorption ◽  
Cement Mortar ◽  
Nitrogen Adsorption ◽  
Accelerated Carbonation ◽  
Molecular Sizes ◽  
The Difference ◽  
Adsorption Desorption

The objective of this work was to examine the microstructural changes caused by the carbonation of normal mortar. Samples were prepared and subjected to accelerated carbonation at 20°C, 65% relative humidity and 20% CO2concentration. The evolutions of the pore size distribution and the specific surface area during carbonation were calculated from the adsorption - desorption isotherms of water vapour and nitrogen. Conflicts observed in the results showed that the porous domains explored by these two methods are not the same due to the difference in molecular sizes of nitrogen and water. These two techniques therefore help to complementarily evaluate the effects of carbonation. The study also helped to explain why results in the literature diverge greatly on the influence of carbonation on specific surface area.

Study of Heating Effect on Specific Surface Area, and Changing Optical Properties of ZnO Nanocrystals

2011 ◽  
Vol 403-408 ◽  
pp. 1205-1210
Author(s):  
Jaleh Babak ◽  
Ashrafi Ghazaleh ◽  
Gholami Nasim ◽  
Azizian Saeid ◽  
Golbedaghi Reza ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Energy Gap ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Zno Nanocrystals ◽  
Transmission Electron ◽  
Zno Nanocrystal

In this work ZnO nanocrystal powders have been synthesized by using Zinc acetate dehydrate as a precursor and sol-gel method. Then the products have been annealed at temperature of 200-1050°C, for 2 hours. The powders were characterized using X-ray diffraction (XRD), UV-vis absorption and photoluminescence (PL) spectroscopy. The morphology of refrence ZnO nanoparticles have been studied using Transmission Electron Microscope (TEM). During the annealing process, increase in nanocrystal size, defects and energy gap quantitative, and decrease in specific surface area have been observed.

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.

Preparation of Nitrogen-Deficient Graphitic Carbon Nitride with a Large Specific Surface Area by Melt Pretreatment and Its Photocatalytic Performance

NANO ◽  
2020 ◽  
Vol 15 (06) ◽  
pp. 2050079
Author(s):  
Xuelei Li ◽  
Jinfeng Bai ◽  
Jiaqi Li ◽  
Chao Li ◽  
Junru Zhang ◽  
...  
Keyword(s):  
Visible Light ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Nitride ◽  
Mesoporous Structure ◽  
Graphitic Carbon ◽  
Graphitic Carbon Nitride ◽  
Large Specific Surface Area ◽  
X Ray

In this study, nitrogen-deficient graphitic carbon nitride (M-LS-g-C3N4) with a mesoporous structure and a large specific surface area was obtained by calcination after melt pretreatment using urea as a precursor. X-ray diffraction (XRD), transmission electron microscopy (TEM), N2 adsorption, X-ray photoelectron spectroscopy (XPS), UV-Vis, ESR and photoluminescence (PL) were used to characterize the structure, morphology and optical performance of the samples. The TEM results showed the formation of a mesoporous structure on the 0.1[Formula: see text]M-LS-g-C3N4 surface. The porous structure led to an increase in the specific surface area from 41.5[Formula: see text]m2/g to 124.3[Formula: see text]m2/g. The UV-Vis results showed that nitrogen vacancies generated during the modification process reduced the band gap of g-C3N4 and improved the visible light absorption. The PL spectra showed that the nitrogen defects promoted the separation of photogenerated electron–hole pairs. In the visible light degradation of methyl orange (MO), the reaction rate constant of 0.1[Formula: see text]M-LS-g-C3N4 reached 0.0086[Formula: see text][Formula: see text], which was 5.05 times that of pure g-C3N4. Superoxide radicals and photogenerated holes were found to be the main active species in the reaction system. This study provides an efficient, green and convenient means of preparing graphitic carbon nitride with a large specific surface area.

Electrochemical Properties of Supercapacitors Using Boron Nitrogen Double-Doped Carbon Nanotubes as Conductive Additive

NANO ◽  
2019 ◽  
Vol 14 (07) ◽  
pp. 1950080
Author(s):  
Hao Hu ◽  
Xiaogang Sun ◽  
Wei Chen ◽  
Jie Wang ◽  
Xu Li ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Double Layer ◽  
Specific Surface Area ◽  
Electric Double Layer ◽  
X Ray ◽  
Nitrogen Doped ◽  
Conductive Additive ◽  
Double Layer Capacitors ◽  
Boron Nitrogen

Carbon nanotubes (CNTs) were doped by ammonium borate as the sources of nitrogen and boron. Under the protection of Ar gas, boron-nitrogen doped CNTs were prepared through nitriding and boronization at high temperature. It is a conductive additive. Then, the obtained CNTs were mixed with activated carbon (AC), SP, sodium dodecyl sulfate (SDS), and cellulose fiber to prepare electrodes. With all the materials, a symmetric electric double-layer supercapacitor (EDLC) was assembled. Next, the materials and electrodes were also characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The factors, chemical connections, and specific surface area of the CNTs were analyzed by X-ray energy spectrum analysis (EDS), X-ray photoelectron spectroscopy (XPS), as well as a specific surface area and porosimetry analyzer (BET). In addition, the electrochemical performances of electric double-layer capacitors were tested with the help of cyclic voltammetry, constant-current charging and discharging, and so on. From the results, we can make a conclusion, that is, both B and N atoms were added into the CNTs and formed bonds successfully with carbon atoms mutually. Besides, the specific surface area is about 1.5 times than that of the CNT. When the charge/discharge current density reaches 50[Formula: see text]mA/g, we can find that the mass specific capacitance of the capacitor can run up to 32.19[Formula: see text]F/g. Also, we observe that the maximum power density is close to 220[Formula: see text]W/kg (700[Formula: see text]mA/g), and the energy density can arrive 9.31[Formula: see text]Wh/kg (50[Formula: see text]mA/g). Based on the impedance test, the electrodes are characterized with low impedance. After 2000 cycles, the boron-nitrogen doped double-layer capacitors maintain a capacitance retention ratio of above 95%. Its power density can still achieve 220[Formula: see text]W/kg when the energy density keeps at 3.46[Formula: see text]Wh/kg. In other words, the electrochemical performance functions of the electric double-layer capacitors are enhanced while the CNTs serve as the electrodes.

The Carbon Deposition during Iron Ore Reduction in Carbon Monoxide

2012 ◽  
Vol 625 ◽  
pp. 243-246
Author(s):  
Shu Hua Geng ◽  
Wei Zhong Ding ◽  
Shu Qiang Guo ◽  
Xiong Gang Lu
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Iron Ore ◽  
Iron Reduction ◽  
Carbon Deposition ◽  
Reduction Process ◽  
Ore Reduction ◽  
X Ray ◽  
Iron Ore Reduction

Iron ore reduction and carbon deposition in pure CO was investigated by using thermogravimetric (TG) method over the temperature range of 0-1200°C. The results of the work may be summarized as follows: in CO stream, carbon deposition occurred below 900°C, no carbon deposition was found above 1000°C. X-Ray analysis of the reacted sample indicated that the carbon deposition occurred with the iron was reduced. The iron reduction process and carbon deposition occurred simultaneously. The rate of carbon deposition changed with the transformation of iron oxides. The specific surface area and pore structure of reduced samples were analyzed. The specific surface area changed with the amount of carbon deposition.

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