scholarly journals Preparation of a Highly Porous Clay-Based Absorbent for Hazard Spillage Mitigation via Two-Step Expansion of Vermiculite

Minerals ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1371
Author(s):  
Duc Cuong Nguyen ◽  
Trung Tuyen Bui ◽  
Yeong Beom Cho ◽  
Yong Shin Kim

Expanded vermiculite (eVMT) has been studied as a risk-free, general-purpose absorbent for liquid hazards due to its excellent thermal and chemical stability. Here, vermiculite was expanded by two steps: exfoliation by 30 wt% H2O2 treatment at 60 °C and subsequent expansion by microwave heating. This two-step expansion produced more homogenously separated concertina-like eVMTs with a higher total pore volume of 7.75 cm3 g−1 than the conventional thermal method. The two-step eVMT was found to be greatly superior to the thermal and commercial silver counterparts in hazardous liquid-uptake performance. The uptake was simply interpreted as a physical infilling process of a liquid into the eVMT pores, and the spontaneous hazard removal with a great capacity was discussed with the large pore volume of two-step eVMT and its suitable pore dimensions for capillary action. As a practical device, a prototype absorbent assembly made of these eVMTs demonstrated the successful mitigation of liquid hazards on an impermeable surface.

2006 ◽  
Vol 49 ◽  
pp. 142-147 ◽  
Author(s):  
H. Ivankovic ◽  
G. Gallego Ferrer ◽  
E. Tkalcec ◽  
M. Ivankovic

Scaffold of hydroxyapatite for further tissue-engineering application was produced by hydrothermal treatment of cuttlefish bone originated aragonite at 200°C. Aragonite (CaCO3) monoliths were completely transformed into hydroxyapatite after 48 hours of HT treatment. The substitution of CO3- groups predominantly into the PO4 3- sites of the Ca10(PO4)6(OH)2 structure was suggested by FTIR spectroscopy. SEM micrographs have shown that the interconnected hollow structure with pillars connecting parallel lamellae in cuttlefish bone is maintained after conversion. Specific surface area (SBET) and total pore volume increased and mean pore size decreased by HT treatment.


2017 ◽  
Vol 54 (2) ◽  
pp. 341-344
Author(s):  
Anda Ionelia Mihai (Voicu) ◽  
Sorina Alexandra Garea ◽  
Eugeniu Vasile ◽  
Cristina Lavinia Nistor ◽  
Horia Iovu

The goal of this paper was to study the modification of porous clay heterostructures (PCHs) with various silane coupling agents. Two commercial coupling agents (3-aminopropyl-triethoxysilane (APTES) and 3-glycidoxypropyl-trimethoxysilane (GPTMS)) with different functional groups (amine and epoxy groups) were used as modifying agents for the PCHs functionalization. The functionalization of PCH with APTES and GPTMS was evaluated by Fourier transform infrared (FTIR) spectrometry, thermogravimetric analysis (TGA), X-Ray Diffractions (XRD) and BET Analysis. FTIR spectra of modified PCHs confirmed the presence of characteristic peaks of silane coupling agents. TGA results highlighted an increase of weight loss for the modified PCHs that was assigned to the degradation of silane coupling agents (APTES and GPTMS) attached to the PCHs. The XRD results showed that the structure of modified PCHs was influenced by the type of the silane coupling agent. The functionalization of PCHs with silane coupling agents was also confirmed by BET analysis. Textural parameters (specific surface area (SBET), total pore volume (Vt )) suggested that the modified PCHs exhibit lower values of SBET and a significant decrease of total pore volume than unmodified PCHs.


Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 298
Author(s):  
Chenlong Ding ◽  
Jinxian He ◽  
Hongchen Wu ◽  
Xiaoli Zhang

Ordos Basin is an important continental shale gas exploration site in China. The micropore structure of the shale reservoir is of great importance for shale gas evaluation. The Taiyuan Formation of the lower Permian is the main exploration interval for this area. To examine the nanometer pore structures in the Taiyuan Formation shale reservoirs in the Lin-Xing area, Northern Shaanxi, the microscopic pore structure characteristics were analyzed via nitrogen adsorption experiments. The pore structure parameters, such as specific surface area, pore volume, and aperture distribution, of shale were calculated; the significance of the pore structure for shale gas storage was analyzed; and the main controlling factors of pore development were assessed. The results indicated the surface area and hole volume of the shale sample to be 0.141–2.188 m2/g and 0.001398–0.008718 cm3/g, respectively. According to the IUPAC (International Union of Pure and Applied Chemistry) classification, mesopores and macropores were dominant in the pore structure, with the presence of a certain number of micropores. The adsorption curves were similar to the standard IV (a)-type isotherm line, and the hysteresis loop type was mainly similar to H3 and H4 types, indicating that most pores are dominated by open type pores, such as parallel plate-shaped pores and wedge-shaped slit pores. The micropores and mesopores provide the vast majority of the specific surface area, functioning as the main area for the adsorption of gas in the shale. The mesopores and macropores provide the vast majority of the pore volume, functioning as the main storage areas for the gas in the shale. Total organic carbon had no notable linear correlation with the total pore volume and the specific surface area. Vitrinite reflectance (Ro) had no notable correlation with the specific surface area, but did have a low “U” curve correlation with the total pore volume. There was no relationship between the quartz content and specific surface area and total pore volume. In addition, there was no notable correlation between the clay mineral content and total specific surface area and total pore volume.


Polymers ◽  
2018 ◽  
Vol 10 (12) ◽  
pp. 1382 ◽  
Author(s):  
Dmitry Alentiev ◽  
Dariya Dzhaparidze ◽  
Natalia Gavrilova ◽  
Victor Shantarovich ◽  
Elena Kiseleva ◽  
...  

New microporous homopolymers were readily prepared from norbornadiene-2,5, its dimer and trimer by addition (vinyl) polymerization of the corresponding monomers with 60–98% yields. As a catalyst Pd-N-heterocyclic carbene complex or Ni(II) 2-ethylhexanoate activated with Na+[B(3,5-(CF3)2C6H3)4]− or methylaluminoxane was used. The synthesized polynorbornenes are cross-linked and insoluble. They are glassy and amorphous polymers. Depending on the nature of the catalyst applied, BET surface areas were in the range of 420–970 m2/g. The polymers with the highest surface area were obtained in the presence of Pd-catalysts from the trimer of norbornadiene-2,5. The total pore volume of the polymers varies from 0.39 to 0.79 cm3/g, while the true volume of micropores was 0.14–0.16 cm3/g according to t-plot. These polymers gave CO2 uptake from 1.2 to 1.9 mmol/g at 273 K and 1 atm. The porous structure of new polymers was also studied by means of wide-angle X-ray diffraction and positron annihilation lifetime spectroscopy.


2018 ◽  
Vol 8 (11) ◽  
pp. 2302 ◽  
Author(s):  
Abdelfattah Amari ◽  
Hatem Gannouni ◽  
Mohammad Khan ◽  
Mohammed Almesfer ◽  
Abubakr Elkhaleefa ◽  
...  

In this study, natural clay minerals with green appearance were treated with sulfuric acid. Mass percentage of acid (wt%), temperature (T), contact time (t) and liquid-to-solid mass ratio (R) are used as the prevailing factors that determine the extent of acid-activation. The values of these factors range from 15–50%, 60–90 °C, 1.5–6 h and 4–7, respectively. The study has focused on the structural changes as well as textural characteristics of the clay. Three activated clay samples were prepared under different treatment conditions. The samples were characterized using X-ray powder diffraction (XRD), fourier transform infrared (FTIR), scanning electron microscope (SEM), chemical analysis and N2 adsorption techniques. Characterization of the treated clay minerals exhibited significant structural changes to a greater extent of acid-activation, from being partially crystalline to being amorphous silica. The surface area and total pore volume of clay increased proportionally with the level of acid treatment. The average pore diameter behaved differently. During the strong acid treatment, a large increase in pore volume and the enlargement of the pore size distribution were observed. This suggests that considerable structural changes and partial destruction may have occurred in this condition. The removal of methylene blue, used as cationic dye, from aqueous solution by the batch adsorption technique on three prepared acid-activated clay samples was studied. The Langmuir model was found to agree well with the experimental data.


2017 ◽  
Vol 11 (5) ◽  
pp. 47 ◽  
Author(s):  
Heman A. Smail ◽  
Kafia M. Shareef ◽  
Zainab H. Ramli

The adsorption of lead (Pb II) ion on different types of synthesized zeolite was investigated. The BET surface area, total pore volume & average pore size distribution of these synthesized zeolites were determined by adsorption isotherms for N2, the surface area & total pore volume of their sources were found by adsorption isothermN2.The adsorption equilibrium was measured after 24h at room temperature (RT) & concentration 10mg.L-1 of Pb (II) was used. The adsorption of heavy metal Pb (II) on four different prepared zeolites (LTA from Montmorillonite clay, FAU(Y)-B.H (G2) from Barley husk, Mordenite (G1) from Chert rock, FAU(X)-S.C (G3) from shale clay & modified Shale clay by oxalic acid (N1) & sodium hydroxide (N2)), were compared with the adsorption of their sources by using static batch experimental method. The major factors affecting the heavy metal ion sorption on different synthesized zeolites & their sources were investigated. The adsorption equilibrium capacity (Qm) of Pb (II) ion for different synthesized zeolites ordered from (N1>N2>LTA>G3>G2>G1&for their sources ordered Shale clay >Montmorilonite> Barley husk>Chert rock. The atomic absorption spectrometry was used for analysis of lead heavy metal ion, the obtained results in this study showed that the different synthesized zeolites were efficient ion exchanges for removing heavy metal, in particular, the modified zeolite from shale clay by oxalic acid.


2018 ◽  
Vol 37 (1) ◽  
pp. 251-272 ◽  
Author(s):  
Junjian Zhang ◽  
Chongtao Wei ◽  
Gaoyuan Yan ◽  
Guanwen Lu

To better understand the structural characteristic of adsorption pores (pore diameter < 100 nm) of coal reservoirs around the coalbed methane production areas of western Yunnan and eastern Guizhou, we analyzed the structural and fractal characteristics of pore size range of 0.40–2.0 nm and 2–100 nm in middle–high rank coals ( Ro,max = 0.93–3.20%) by combining low-temperature N2/CO2 adsorption tests and surface/volume fractal theory. The results show that the coal reservoirs can be divided into three categories: type A ( Ro,max < 2.15%), type B (2.15% <  Ro,max <2.50%), and type C ( Ro,max > 2.15%). The structural parameters of pores in the range from 2 to 100 nm are influenced by the degree of coal metamorphism and the compositional parameters (e.g., ash and volatile matter). The dominant diameters of the specific surface areas are 10–50 nm, 2–50 nm, and 2–10 nm, respectively. The pores in the range from <2 nm provide the largest proportion of total specific surface area (97.22%–99.96%) of the coal reservoir, and the CO2-specific surface area and CO2-total pore volume relationships show a positive linear correlation. The metamorphic degree has a much greater control on the pores (pore diameter less than 2 nm) structural parameters than those of the pore diameter ranges from 2 to 100 nm. Dv1 and Dv2 can characterize the structure of 2–100 nm adsorption pores, and Dv1 (volume heterogeneity) has a positive correlation with the pore structural parameters such as N2-specific surface area and N2-total pore volume. This parameter can be used to characterize volume heterogeneity of 2–10 nm pores. Dv2 (surface heterogeneity) showed type A > type B > type C and was mainly affected by the metamorphism degree. Ds2 can be used to characterize the pore surface heterogeneity of micropores in the range of 0.62–1.50 nm. This parameter has a good correlation with the pore parameters (CO2-total pore volume, CO2-specific surface area, and average pore size) and is expressed as type C < type B < type A. In conclusion, the heterogeneity of the micropores is less than that of the meso- and macropores (2–100 nm). Dv1, Dv2, and Ds2 can be used as effective parameters to characterize the pore structure of adsorption pores. This result can provide a theoretical basis for studying the pore structure compatibility of coal reservoirs in the region.


2020 ◽  
Vol 55 (3) ◽  
pp. 221-228
Author(s):  
HA Simol ◽  
R Sultana ◽  
M Y A Mollah ◽  
MS Miran

Nanocrystalline Fe3O4 and Fe2O3 particles were successfully synthesized by an innovative hybrid electrochemical-thermal method. The as-prepared compound was calcined for an hour from 100 to 600oC temperatures. The crystallinity, morphology and chemical state of the synthesized powders were characterized by XRD, TG-DTA, SEM/EDS, FT-IR, and UV–Vis spectral techniques after calcinations. The Brunauer–Emmett–Teller (BET) plots confirmed that iron oxide nanoparticles (NPs) calcined at 400oC has a surface area of 18.28 m2 g-1 with a total pore volume of 0.2064 cc g-1. From XRD pattern it is revealed that the precursor calcined at lower temperature (100-400oC) correspond to Fe3O4,while the ones calcined at higher temperature follow Fe2O3 pattern. The morphology of iron oxide NPs calcined at different temperatures were studied with scanning electron microscope (SEM) and exhibits spherical shaped geometries with average diameters of 80-150nm. Bangladesh J. Sci. Ind. Res.55(3), 221-228, 2020


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