Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption

2020 ◽  
Vol 56 (49) ◽  
pp. 6715-6718 ◽  
Author(s):  
Zi-Jian Li ◽  
Yu Ju ◽  
Bowen Yu ◽  
Xiaoling Wu ◽  
Huangjie Lu ◽  
...  
Keyword(s):  
Single Crystals ◽  
Surface Area ◽  
Pore Volume ◽  
Bet Surface Area ◽  
Void Space ◽  
Adsorption Capacities ◽  
Iodine Adsorption

Isoreticular expansion of Th-MOFs via modulated synthesis yielded seven hierarchical complexes with superior quality single crystals, record high void space and BET surface area among Th materials, and exceptional iodine adsorption capacities.

scholarly journals An Eco-Friendly Process for Removal of Lead from Aqueous Solution

2017 ◽  
Vol 11 (5) ◽  
pp. 47 ◽  
Author(s):  
Heman A. Smail ◽  
Kafia M. Shareef ◽  
Zainab H. Ramli
Keyword(s):  
Heavy Metal ◽  
Oxalic Acid ◽  
Surface Area ◽  
Pore Volume ◽  
Metal Ion ◽  
Adsorption Equilibrium ◽  
Total Pore Volume ◽  
Heavy Metal Ion ◽  
Bet Surface Area ◽  
Barley Husk

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.

scholarly journals Surface and Catalytic Properties of γ-Irradiated Cr2O3/Al2O3 Solids

1997 ◽  
Vol 15 (6) ◽  
pp. 465-476 ◽  
Author(s):  
G.A. El-Shobaky ◽  
A.M. Ghozza ◽  
G.M. Mohamed
Keyword(s):  
Catalytic Activity ◽  
Co Oxidation ◽  
Surface Area ◽  
Pore Volume ◽  
Active Sites ◽  
Catalytic Properties ◽  
Total Pore Volume ◽  
Bet Surface Area ◽  
Two Samples ◽  
Γ Rays

Two samples of Cr2O3/Al2O3 were prepared by mixing a known mass of finely powdered Al(OH)3 with a calculated amount of CrO3 solid followed by drying at 120°C and calcination at 400°C. The amounts of chromium oxide employed were 5.66 and 20 mol% Cr2O3, respectively. The calcined solid specimens were then treated with different doses of γ-rays (20–160 Mrad). The surface and catalytic properties of the different irradiated solids were investigated using nitrogen adsorption at −196°C and the catalysis of CO oxidation by O2 at 300–400°C. The results revealed that γ-rays brought about a slight decrease in the BET surface area, SBET (15%), and in the total pore volume, Vp (20%), of the adsorbent containing 5.66 mol% Cr2O3. The same treatment increased the total pore volume, Vp (36%), and the mean pore radius, r̄ (43%), of the other adsorbent sample without changing its BET surface area. The catalytic activities of both catalyst samples were found to increase as a function of dose, reaching a maximum value at 80–160 Mrad and 40 Mrad for the solids containing 5.66 and 20 mol% Cr2O3, respectively. The maximum increase in the catalytic activity measured at 300°C was 59% and 100% for the first and second catalyst samples, respectively. The induced effect of γ-irradiation on the catalytic activity was an increase in the concentration of catalytically active sites taking part in chemisorption and in the catalysis of CO oxidation by O2 without changing their energetic nature. This was achieved by a progressive removal of surface hydroxy groups during the irradiation process.

Synthesis and Preparation of Al-MCM-41 Mesoporous Materials Using Oil Shale Residue

2019 ◽  
Vol 944 ◽  
pp. 1192-1198
Author(s):  
Rong Wang ◽  
Zhi Xiang Lin ◽  
Yang Zhao ◽  
Xiao Dong Xu ◽  
Yan Xi Deng
Keyword(s):  
Surface Area ◽  
Mesoporous Materials ◽  
Pore Volume ◽  
Oil Shale ◽  
Bet Surface Area ◽  
Ammonium Bromide ◽  
Scale Production ◽  
Scanning Electron Micrographs ◽  
One Step ◽  
Mcm 41

An Al-supported cage-like mesoporous silica type MCM-41 has been prepared using a simple one-step synthetic procedure using oil shale residue and CTAB(Hexadecyl trimethyl Ammonium Bromide) as the template. The effects of temperature on the porosity, structure and surface area of Al-MCM-41 mesoporous materials were characterized by X-ray powder diffraction, N2adsorption desorption, scanning electron micrographs (SEM), transmission electron microscopy (TEM) techniques and Fourier transform infrared spectroscopy (FT-IR). The results indicated that temperature was a key to the characteristics of Al-MCM-41 materials, and when the temperature up to 333 K, Al-MCM-41 exhibited excellent characteristics with high degree of order, high surface area and pore volume. The one-step hydrothermal synthesized MCM-41 mesoporous material possessed high BET surface area, high pore size and high pore volume. They are respectively 835.1 m2/g, 32.6 Å and 1.22 cm3/g under the condition of the Si : Al =78:1, pH =10, crystallization temperature was 333K, crystallization time was 48h and calcination at 823 K for 5 h in air. All the results indicated the possibility of using oil shale residue as silicon and aluminum source to produce Al-MCM-41, and gave us a new way to recycle a solid waste. As well as this made it impossible to large-scale production of Al-MCM-41. Keywords: Al-MCM-41 mesoporous materials, oil shale residue, one-step synthesis

scholarly journals Carbonization Temperature Effect over Activated Carbon Porosity Derived from Industrial Processing Waste

2019 ◽  
Vol 2 (3) ◽  
pp. 1205-1209
Author(s):  
Hasan Sayğılı
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Pore Volume ◽  
Activated Carbons ◽  
Waste Product ◽  
Total Pore Volume ◽  
Carbonization Temperature ◽  
Bet Surface Area ◽  
Processing Waste ◽  
Industrial Processing

The influence of carbonization temperature (CT) on pore properties of the prepared activated carbon using lentil processing waste product (LWP) impregnated with potassium carbonate was studied. Activated carbons (ACs) were obtained by impregnation with 3:1 ratio (w/w) K2CO3/LWP under different carbonization temperatures at 600, 700, 800 and 900 oC for 1h. Activation at low temperature represented that micropores were developed first and then mesoporosity developed, enhanced up to 800 oC and then started to decrease due to possible shrinking of pores. The optimum temperature for LWP was found to be around 800 oC on the basis of total pore volume and the Brunauer-Emmett-Teller (BET) surface area. The optimum LWPAC sample was found with a CT of 800 oC, which gives the highest BET surface area and pore volume of 1875 m2/g and 0.995 cm3/g, respectively.

scholarly journals Porous Lactose as a Novel Ingredient Carrier for the Improvement of Quercetin Solubility In Vitro

2021 ◽  
Vol 2021 ◽  
pp. 1-6
Author(s):  
Wen Liu ◽  
Tong-Tong Wang ◽  
Xiao-Luan Tang ◽  
Fei-Ya Jiang ◽  
Xiao Yan ◽  
...  
Keyword(s):  
Surface Area ◽  
Pore Volume ◽  
Reduction Rate ◽  
Xrd Analysis ◽  
Bet Surface Area ◽  
Pore Width ◽  
Release Rates ◽  
Loading Efficiency ◽  
Highly Porous

In this work, quercetin was loaded in the highly-porous lactose via the adsorption of quercetin molecules in ethanol. The method aims to improve the quercetin solubility and the loading capacity of lactose. The method relates to the synthesis of the highly-porous lactose with a particle size of ∼35 μm, a mean pore width of ∼30 nm, a BET surface area of 35.0561 ± 0.4613 m2/g, and a BJH pore volume of ∼0.075346 cc/g. After the quercetin loading in ethanol, BET surface area and BJH pore volume of porous lactose were reduced to 28.8735 ± 0.3526 m2/g and 0.073315 cc/g, respectively. The reduction rate was based on the quercetin loading efficiency of highly-porous lactose. DSC analysis and XRD analysis suggest that the sediments of quercetin in the nanopores of porous lactose are crystalline. FTIR spectroscopy results suggest that there is no significant interaction between quercetin and lactose. The highly-porous lactose had a higher loading efficiency of 20.3% (w/w) compared to the α-lactose (with 5.2% w/w). The release rates of quercetin from the highly-porous lactose tablets were faster compared to the conventional α-lactose carrier.

scholarly journals The Synthesis of a Novel Tröger Base Polymer of 2,6(7)-Diamino-9,9,10,10-Tetramethyl-9,10-Dihydroanthracene

2018 ◽  
Vol 34 (5) ◽  
pp. 2661-2666
Author(s):  
Sadiq A. Karim
Keyword(s):  
Thermal Stability ◽  
Surface Area ◽  
Pore Volume ◽  
Total Pore Volume ◽  
Bet Surface Area ◽  
Synthesis Process ◽  
Good Thermal Stability ◽  
Good Solubility ◽  
Base Polymer

Condensation polymerisation technique has been employed to synthesise a Novel Tröger base polymer with thermal stability and microporosity. The synthesis process starts with alkylating anthracene, then nitrating and reducing this to produce the monomer. A Tröger base polymer is obtained by polymerising the monomer to afford a white polymer with good solubility into dichloromethane and chloroform, good thermal stability to ~377oC and a good BET surface area of 368.6 m2/g with a total pore volume of 0.4166 ml/g.

A Novel Zeolite-Containing Composite Material Synthesized via In Situ Crystallization

2014 ◽  
Vol 926-930 ◽  
pp. 32-35
Author(s):  
Shu Qin Zheng ◽  
Shao Ren ◽  
Jian Ce Zhang ◽  
Wei Zhu
Keyword(s):  
Composite Material ◽  
Surface Area ◽  
Pore Volume ◽  
Reaction Medium ◽  
Pronounced Effect ◽  
Bet Surface Area ◽  
Y Zeolite ◽  
Relative Crystallinity

A novel Y zeolite-containing composite material was prepared via in situ crystallization with sepiolite and catalyst residue as starting materials, of which the BET surface area is up to 582 m2/g, the pore volume is 0.43 cm3/g, the relative crystallinity is as high as 55.7 %, the surface is smooth and regular, and Y zeolite particles are in the range of 0.4-1.0 mirons, the composite contains large number Y zeolite with more meso-macro porous structure.The alkalinity in reaction medium has a pronounced effect on the relative crystallinity of Y zeolite.

CuO/CeO2 and CuO/PrO2-CeO2 Catalysts for Preferential Oxidation of CO

2013 ◽  
Vol 773 ◽  
pp. 601-605 ◽  
Author(s):  
Zhi Jun Zhao ◽  
Ruo Yu Wang ◽  
Qian Long Zhao ◽  
En Peng Wang ◽  
Hai Quan Su ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Hydrothermal Method ◽  
Surface Area ◽  
Pore Volume ◽  
Crucial Role ◽  
Textural Properties ◽  
Bet Surface Area ◽  
Oxidation Of Co ◽  
Preferential Oxidation Of Co ◽  
Adsorption Desorption

The CuO/CeO2and CuO/PrO2-CeO2catalysts were prepared by the hydrothermal method, and characterized via XRD, SEM and N2adsorption-desorption techniques. The study shows that the BET surface area and pore volume of the CuO/PrO2-CeO2catalysts increase with the increase of praseodymium content. The CuO/CeO2catalyst presents higher catalytic activity in compare with the CuO/PrO2-CeO2catalysts although the addition of praseodymium promotes textural properties of the CuO/CeO2catalysts, and it proves that the interaction of CuO and CeO2has a crucial role in CO-PROX.

scholarly journals On the Gas Storage Properties of 3D Porous Carbons Derived from Hyper-Crosslinked Polymers

Polymers ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 588 ◽  
Author(s):  
Giorgio Gatti ◽  
Mina Errahali ◽  
Lorenzo Tei ◽  
Maurizio Cossi ◽  
Leonardo Marchese
Keyword(s):  
Thermal Treatment ◽  
Surface Area ◽  
Pore Volume ◽  
Chemical Activation ◽  
Chemical Characterization ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Gas Storage ◽  
Bet Surface Area ◽  
Porous Carbons

The preparation of porous carbons by post-synthesis treatment of hypercrosslinked polymers is described, with a careful physico-chemical characterization, to obtain new materials for gas storage and separation. Different procedures, based on chemical and thermal activations, are considered; they include thermal treatment at 380 °C, and chemical activation with KOH followed by thermal treatment at 750 or 800 °C; the resulting materials are carefully characterized in their structural and textural properties. The thermal treatment at temperature below decomposition (380 °C) maintains the polymer structure, removing the side-products of the polymerization entrapped in the pores and improving the textural properties. On the other hand, the carbonization leads to a different material, enhancing both surface area and total pore volume—the textural properties of the final porous carbons are affected by the activation procedure and by the starting polymer. Different chemical activation methods and temperatures lead to different carbons with BET surface area ranging between 2318 and 2975 m2/g and pore volume up to 1.30 cc/g. The wise choice of the carbonization treatment allows the final textural properties to be finely tuned by increasing either the narrow pore fraction or the micro- and mesoporous volume. High pressure gas adsorption measurements of methane, hydrogen, and carbon dioxide of the most promising material are investigated, and the storage capacity for methane is measured and discussed.

Sign in / Sign up

Export Citation Format

Share Document