scholarly journals Quaternary functionalized mesoporous adsorbents for ultra-high kinetics of CO2 capture from air

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Tao Wang ◽  
Xinru Wang ◽  
Chenglong Hou ◽  
Jun Liu
Keyword(s):  
Pore Structure ◽  
Carbon Capture ◽  
Large Scale ◽  
Functional Group ◽  
Capillary Condensation ◽  
High Surface ◽  
High Surface Area ◽  
Atmospheric Environment ◽  
Cylindrical Pore ◽  
Cyclic Adsorption

AbstractObstacles to widespread deployments of direct air capture of CO2 (DAC) lie in high material and energy costs. By grafting quaternary ammonium (QA) functional group to mesoporous polymers with high surface area, a unique DAC adsorbent with moisture swing adsorption (MSA) ability and ultra-high kinetics was developed in this work. Functionalization is designed for efficient delivery of QA group through mesopores to active substitution sites. This achieved ultra-high kinetics adsorbent with half time of 2.9 min under atmospheric environment, is the highest kinetics value reported among DAC adsorbents. A cyclic adsorption capacity of 0.26 mmol g−1 is obtained during MSA process. Through adsorption thermodynamics, it is revealed that adsorbent with uniform cylindrical pore structure has higher functional group efficiency and CO2 capacity. Pore structure can also tune the MSA ability of adsorbent through capillary condensation of water inside its mesopores. The successful functionalization of mesoporous polymers with superb CO2 adsorption kinetics opens the door to facilitate DAC adsorbents for large-scale carbon capture deployments.

High Cr(VI) Adsorption Performance of Coal-Based Activated Carbon in Aqueous Solution

2013 ◽  
Vol 798-799 ◽  
pp. 1123-1127
Author(s):  
Hua Lei Zhou ◽  
Qiong Qiong Zhu ◽  
Dong Hua Huang
Keyword(s):  
Aqueous Solution ◽  
Activated Carbon ◽  
Pore Structure ◽  
Ph Value ◽  
High Surface ◽  
High Surface Area ◽  
Koh Activation ◽  
Transmission Electron ◽  
Mesoporous Adsorbent ◽  
Initial Ph

The activated carbon with high surface area was prepared by KOH activation from anthracite and used as adsorbent for removal of Cr (VI) from aqueous solution. The pore structure and surface properties were characterized by N2 adsorption at 77K, transmission electron microscope (TEM) and Fourier transform infrared spectroscopy ( FTIR). Effect of pH and isotherms at different temperature were investigated. Results show that the prepared carbon is a microporous-and mesoporous-adsorbent with developed pore structure and abundant surface oxygen-containing groups. PH value of the solution plays key function on the adsorption. The chemical adsorption dominates the adsorption process. The activated carbon exhibits much higher Cr adsorption capacity than the commercial activated carbon at initial pH of ~3. The equilibrium adsorption data are fitted by both Freundlich model and Langmuir model well.

Carbon Dioxide Sequestration Using Activated Carbon From Agro Waste-Waste Bamboo

2021 ◽  
Author(s):  
Emmanuel Ayodele ◽  
Victoria Ezeagwula ◽  
Precious Igbokwubiri
Keyword(s):  
Activated Carbon ◽  
Fly Ash ◽  
Greenhouse Gases ◽  
Surface Area ◽  
Carbon Capture ◽  
Agricultural Waste ◽  
High Surface ◽  
Research Work ◽  
High Surface Area ◽  
Bet Surface Area

Abstract Bamboo trees are one of the fastest growing trees in tropical rainforests around the world, they have various uses ranging from construction to fly ash generation used in oil and gas cementing, to development of activated carbon which is one of the latest uses of bamboo trees. This paper focuses on development of activated carbon from bamboo trees for carbon capture and sequestration. The need for improved air quality becomes imperative as the SDG Goal 12 and SDG Goal13 implies. One of the major greenhouse gases is CO2 which accounts for over 80% of greenhouse gases in the environment. Eliminating the greenhouse gases without adding another pollutant to the environment is highly sought after in the 21st century. Bamboo trees are mostly seen as agricultural waste with the advent of scaffolding and other support systems being in the construction industry. Instead of burning bamboo trees or using them for cooking in the local communities which in turn generates CO2 and fly ash, an alternative was considered in this research work, which is the usage of bamboo trees to generate activated, moderately porous and high surface area carbon for extracting CO2 from various CO2 discharge sources atmosphere and for water purification. This paper focuses on the quality testing of activated carbon that can effectively absorb CO2. The porosity, pore volume, bulk volume, and BET surface area were measured. The porosity of the activated carbon is 27%, BET surface area as 1260m²/g. Fixed carbon was 11.7%, Volatility 73%, ash content 1.7%.

Facile and large-scale synthesis of poly(m-phenylenediamine) nanobelts with high surface area and superior dye adsorption ability

RSC Advances ◽  
2014 ◽  
Vol 4 (85) ◽  
pp. 45244-45250 ◽  
Author(s):  
Yun Meng ◽  
Liyuan Zhang ◽  
Liyuan Chai ◽  
Wanting Yu ◽  
Ting Wang ◽  
...  
Keyword(s):  
Surface Area ◽  
Large Scale ◽  
High Surface ◽  
High Surface Area ◽  
Dye Adsorption ◽  
High Adsorption ◽  
Adsorption Ability ◽  
Adsorption Performance ◽  
Large Scale Synthesis

PmPD nanobelts with high adsorption performance have been synthesized by using CTAP as oxidants.

scholarly journals Green and facile synthesis of cerium doped Ni3Fe electrocatalyst for efficient oxygen evolution reaction

2020 ◽  
Vol 34 (2) ◽  
pp. 353-363
Author(s):  
F. Kanwal ◽  
A. Batool ◽  
R. Akbar ◽  
S. Asim ◽  
M. Saleem
Keyword(s):  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Large Scale ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Three Dimensional ◽  
Alkaline Electrolyte ◽  
Hydrogen Electrode ◽  
Molar Ratios

Electrochemical water splitting is the most promising pathway to produce high-purity hydrogen to alleviate global energy crisis. This reaction demands inexpensive, efficient and robust electrocatalyst for its commercial use. Herein, we demonstrate an effective, facile and scalable method for the synthesis of cerium doped Ni3Fe nanostructures as an electrocatalyst for oxygen evolution reaction (OER) by following simple chemical bath deposition route. The different molar ratios (3, 6 and 12 mM) of cerium in the chemical bath were used to study its effect on the structural and the electrochemical properties of the Ni3Fe nanostructured films. Doping of cerium contents induced variations in the morphology of deposited Ni3Fe nanostructures. The optimized electrocatalyst Ni3Fe/Ce-6 yielded high surface area catalyst nanosheets uniformly deposited on three-dimensional conductive scaffold to ensure increase in the exposure of doped Ni3Fe catalytic sites with high electrical conductivity. As a result, this earth-abundant electrocatalyst affords high OER performance with a small overpotential of 310 mV versus reversible hydrogen electrode (RHE) at 10 mA cm-2 and retains good stability up to ~ 10 h in alkaline electrolyte. This scalable strategy has great potential in future advancement of efficient and low-cost electrocatalysts for their large-scale application in energy conversion systems.                     KEY WORDS: Oxygen evolution, Electrocatalyst, Ni3Fe nanostructures, Cerium, Alkaline electrolyte   Bull. Chem. Soc. Ethiop. 2020, 34(2), 353-363 DOI: https://dx.doi.org/10.4314/bcse.v34i2.12

Large-scale and facile synthesis of a porous high-entropy alloy CrMnFeCoNi as an efficient catalyst

2020 ◽  
Vol 8 (35) ◽  
pp. 18318-18326 ◽  
Author(s):  
Hailong Peng ◽  
Yangcenzi Xie ◽  
Zicheng Xie ◽  
Yunfeng Wu ◽  
Wenkun Zhu ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Surface Area ◽  
Large Scale ◽  
High Surface ◽  
High Surface Area ◽  
Catalytic Performance ◽  
High Entropy Alloy ◽  
Facile Synthesis ◽  
Efficient Catalyst ◽  
High Entropy

Porous high entropy alloy CrMnFeCoNi exhibited remarkable catalytic activity and stability toward p-nitrophenol hydrogenation. The enhanced catalytic performance not only resulted from the high surface area, but also from exposed high-index facets with terraces.

Preparation of Highly Crystalline Mesoporous TiO2 by Using Carbon to Protect the Pore Structure at Elevated Temperature

2010 ◽  
Vol 654-656 ◽  
pp. 2406-2409
Author(s):  
Yu Dan Zhu ◽  
Yu Lan Ding ◽  
Xiao Hua Lu ◽  
Wei Zhuang ◽  
Ling Hong Lu
Keyword(s):  
Elevated Temperature ◽  
Pore Structure ◽  
Anatase Phase ◽  
High Surface ◽  
Catalyst Support ◽  
High Surface Area ◽  
Pore Wall ◽  
Mesoporous Tio2 ◽  
Mesopore Structure ◽  
Novel Strategy

Mesoporous TiO2 with highly crystalline pore wall has an enormous potential for applications in photocatalysis, catalyst support, drug delivery, etc. However, with the sintering temperature increasing, the crystallinity of the pore wall increases while the mesopore structure tends to collapse. In this work, we presented a novel strategy for creating highly crystalline mesoporous TiO2 (MT800) by using carbon to protect the pore structure at elevated temperature. The structural characterization indicates that MT800 has highly crystalline anatase phase and processes high surface area. The photocatalysis performance was evaluated by organic degradation and the results show that MT800 has superior photocatalysis activity to the TiO2 (T800) calcined at 800°C without carbon, because of the synergies of crystallinity and mesostructure.

scholarly journals Synthesis and characterization of porous silica and polyaniline-porous silica composite materials with high surface area

2014 ◽  
Vol 49 (1) ◽  
pp. 1-8
Author(s):  
US Akhtar ◽  
MK Hossain ◽  
MS Miran ◽  
MYA Mollah
Keyword(s):  
Electron Microscopy ◽  
Pore Size ◽  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Porous Silica ◽  
Nitrogen Adsorption ◽  
High Specific Surface Area ◽  
Molar Ratio ◽  
Cylindrical Pore

Porous silica materials were synthesized from tetraethyl orthosilicate (TEOS) using Pluronic P123 (non-ionic triblock copolymer, EO20PO70O20) as template under acidic conditions which was then used to prepare polyaniline (PAni) and porous silica composites (PAnisilica) at a fixed molar ratio. These materials were characterized by nitrogen adsorption-desorption isotherm measured by Barrett-Joyner- Halenda (BJH) method and pore size distribution from desorption branch and surface area measured by the Brunauer-Emmett-Teller (BET) method, scanning electron microscopy (SEM), transmission electron microscopy (TEM), TEM-energy dispersive X-ray (EDX) and Fourier transform infrared (FT-IR) spectroscopy. The composite maintains its structure even after the polymerization and the polymer is dispersed on the inorganic matrix. The rod-like porous silica was about 1?m to 1.5 ?m long and on an average the diameter was in the range of 300- 500 nm. The SEM and TEM images show well ordered 2d hexagonal pore, high specific surface area (850 m2g-1) and uniform pore size of ca. 6.5 nm in diameter. After incorporation of PAni inside the silica pore, framework of porous silica did not collapse and the surface area of the composite was as high as 434 m2g-1 which was 5.5 time higher than our previous report of 78.3 m2g-1. Due to shrinkage of the framework during the incorporation of aniline inside the silica, the pore diameter slightly increase to 7.5 nm but still showing Type IV isotherm and typical hysteresis loop H1 implying a uniform cylindrical pore geometry. DOI: http://dx.doi.org/10.3329/bjsir.v49i1.18847 Bangladesh J. Sci. Ind. Res. 49(1), 1-8, 2014

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