scholarly journals Activated Carbon Produced by Pyrolysis of Waste Wood and Straw for Potential Wastewater Adsorption

Materials ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2047 ◽  
Author(s):  
Katarzyna Januszewicz ◽  
Paweł Kazimierski ◽  
Maciej Klein ◽  
Dariusz Kardaś ◽  
Justyna Łuczak

Pyrolysis of straw pellets and wood strips was performed in a fixed bed reactor. The chars, solid products of thermal degradation, were used as potential materials for activated carbon production. Chemical and physical activation processes were used to compare properties of the products. The chemical activation agent KOH was chosen and the physical activation was conducted with steam and carbon dioxide as oxidising gases. The effect of the activation process on the surface area, pore volume, structure and composition of the biochar was examined. The samples with the highest surface area (1349.6 and 1194.4 m2/g for straw and wood activated carbons, respectively) were obtained when the chemical activation with KOH solution was applied. The sample with the highest surface area was used as an adsorbent for model wastewater contamination removal.

2010 ◽  
Vol 658 ◽  
pp. 113-116 ◽  
Author(s):  
Chiravoot Pechyen ◽  
Duangdao Aht-Ong ◽  
Viboon Sricharoenchaikul ◽  
Duangduen Atong

Pyrolysis is one form of energy recovery process which has the potential to generate oil, gas and char products. The char becomes an attractive by-product, with applications including production of activated carbons that is useful as a sorbent for wastewater treatment and air pollution control. In this work, activated carbon was prepared from Coffee (Coffea Arabica L.) bean waste collected from local coffee houses. Char from pyrolysis of coffee bean waste at 900 °C contained high fixed carbon and low volatile content that was favorable for subsequent activation process. The char was activated via chemical treatment with sodium hydroxide (NaOH) at five different NaOH : char ratios (1:1, 2:1, 3:1, 4:1 and 5:1) and heat treated at 400°C for 15 minutes using a fixed bed reactor under nitrogen atmosphere with a flow rate of 100 mL/min. Result shows that NaOH works effectively as dehydration reagent around 400°C. Under the experimental conditions investigated, impregnation ratio of 1.0 was found to be suitable for producing high-surface area activated carbon. The surface area and total pore volume of activated carbons, which were determined by application of the Brunauer–Emmett–Teller (BET) and t-plot methods, were achieved as high as 802 m2/g and 0.80 cm3/g, respectively. The chemically activated carbons were found to be mainly type I carbons and had high adsorption property (Methylene blue adsorption = 284 mg/g and Iodine number = 1070 mg/g).


2020 ◽  
Vol 15 (2) ◽  
pp. 79-89
Author(s):  
Sriatun Sriatun ◽  
Shabrina Herawati ◽  
Icha Aisyah

The starting material for activated carbon was biomass from teak woodcutting, which consists of 47.5% cellulose, 14.4% hemicellulose, and 29.9% lignin. The surface area and iodine number of activated carbons are the factors determining the adsorption ability. This study aims to determine the effect of the activator type on activated carbon characters and test the absorption ability for waste cooking oil. The synthesis stages include carbonization, chemical activation, and then physics activation. The activation process consists of two steps. Firstly, the chemical activation via adding H2SO4, and H3PO4 at room temperature for 24 hours, the second, physical activation by heating at various temperatures of 300, 400, and 500 °C for two hours. The characterizations of activated carbon include water content, ash content, iodine number, functional groups, and surface area. Furthermore, the activated carbon was used as an adsorbent for waste cooking oil for 60 minutes at 100 °C with a stirring of 500 rpm. The results were analyzed using UV-Vis spectrophotometry at a maximum wavelength of 403 nm. The iodine numbers of activated carbon ranged 481.1-1211.4 mg/g and 494.8-1204 mg/g for H3PO4 and H2SO4, respectively.Activated carbon with H3PO4 of 15% and an activation temperature of 400 °C has the highest surface area of 445.30 m2/g.  The H2SO4 dan H3PO4 activators can be used to improve the quality of activated carbon in absorbing dyes in waste cooking oil, where the optimum concentration is 10-15% (v/v). The H3PO4 activator tends to produce a higher bleaching percentage than H2SO4. 


Processes ◽  
2019 ◽  
Vol 7 (9) ◽  
pp. 592 ◽  
Author(s):  
Chao Ge ◽  
Dandan Lian ◽  
Shaopeng Cui ◽  
Jie Gao ◽  
Jianjun Lu

Low-cost activated carbons were prepared from waste polyurethane foam by physical activation with CO2 for the first time and chemical activation with Ca(OH)2, NaOH, or KOH. The activation conditions were optimized to produce microporous carbons with high CO2 adsorption capacity and CO2/N2 selectivity. The sample prepared by physical activation showed CO2/N2 selectivity of up to 24, much higher than that of chemical activation. This is mainly due to the narrower microporosity and the rich N content produced during the physical activation process. However, physical activation samples showed inferior textural properties compared to chemical activation samples and led to a lower CO2 uptake of 3.37 mmol·g−1 at 273 K. Porous carbons obtained by chemical activation showed a high CO2 uptake of 5.85 mmol·g−1 at 273 K, comparable to the optimum activated carbon materials prepared from other wastes. This is mainly attributed to large volumes of ultra-micropores (<1 nm) up to 0.212 cm3·g−1 and a high surface area of 1360 m2·g−1. Furthermore, in consideration of the presence of fewer contaminants, lower weight losses of physical activation samples, and the excellent recyclability of both physical- and chemical-activated samples, the waste polyurethane foam-based carbon materials exhibited potential application prospects in CO2 capture.


Materials ◽  
2020 ◽  
Vol 13 (20) ◽  
pp. 4658 ◽  
Author(s):  
Katarzyna Januszewicz ◽  
Anita Cymann-Sachajdak ◽  
Paweł Kazimierski ◽  
Marek Klein ◽  
Justyna Łuczak ◽  
...  

In this work, we present the preparation and characterization of biomass-derived activated carbon (AC) in view of its application as electrode material for electrochemical capacitors. Porous carbons are prepared by pyrolysis of chestnut seeds and subsequent activation of the obtained biochar. We investigate here two activation methods, namely, physical by CO2 and chemical using KOH. Morphology, structure and specific surface area (SSA) of synthesized activated carbons are investigated by Brunauer-Emmett-Teller (BET) technique and scanning electron microscopy (SEM). Electrochemical studies show a clear dependence between the activation method (influencing porosity and SSA of AC) and electric capacitance values as well as rate capability of investigated electrodes. It is shown that well-developed porosity and high surface area, achieved by the chemical activation process, result in outstanding electrochemical performance of the chestnut-derived porous carbons.


2012 ◽  
Vol 506 ◽  
pp. 214-217 ◽  
Author(s):  
Athiwat Sirimuangjinda ◽  
Khanthima Hemra ◽  
Duangduen Atong ◽  
Chiravoot Pechyen

Pyrolysis is one form of energy recovery process which has the potential to generate oil, gas and char products. The char becomes an attractive by-product, with applications including production of activated carbons, which is useful as a ethylene sorbent for climacteric fruit packaging. In this work, activated carbon prepared from waste tire, produced as a by product of the bio-diesel extraction industry was prepared via chemical treatment with phosphoric acid (H3PO4) at three different char:H3PO4 ratios (1:1, 1:2 and 1:3) under fixed bed pyrolysis at 400, 500 and 600°C for 30 minutes in nitrogen (N2) flow rate of 1000 mL/min and heating rate of 20°C/min. Result shows that char pyrolyzed at 800°C contained high fixed carbon and low volatile content favorable for subsequent activation process compared to other cases.(data not show here) Under the experimental conditions investigated, impregnation ratio of 1:2 were found to be suitable for producing high-surface area activated carbon. It was shown that H3PO4 did work effectively as dehydration reagent at approximately 600°C. The obtained carbons were characterized by nitrogen adsorptiondesorption isotherms at-196 °C. The surface area of activated carbons, which were determined by application of the BrunauerEmmettTeller (BET) and t-plot methods, were achieved as high as 833.50 m2/g. The chemically activated carbons were found to be mainly type II carbons and high adsorption property (Methylene blue adsorption = 622 mg/g and Iodine number = 899 mg/g).


2021 ◽  
Vol 2117 (1) ◽  
pp. 012040
Author(s):  
A Budianto ◽  
E Kusdarini ◽  
W Mangkurat ◽  
E Nurdiana ◽  
N P Asri

Abstract Young Coconut products have many benefits for society as for drinks and medicine, and it produces young Coconut shells and coir waste. The contents of cellulose and carbon elements are interesting to be utilized to be activated carbon. This research aimed to know the activator concentration of hydroxide potassium chemical and heating physical with microwave electrical power to produce activated carbon products. This research was conducted in laboratory experiments with chemical and physical activation methods, measuring proximate and iodine product numbers. The result showed that activated carbon from young Coconuts shells and coir with activation process used chemical activation and produced activated carbon products that met SNI standard number 06-3730-1995. Iodine number of activated carbons was in the range of 1776.60 mg/g – 2220.75 mg/g, iodine number as more than 23.5% of SNI Standard.


Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2951
Author(s):  
Mirosław Kwiatkowski ◽  
Jarosław Serafin ◽  
Andy M. Booth ◽  
Beata Michalkiewicz

This paper presents the results of a computer analysis of the effect of activation process temperature on the development of the microporous structure of activated carbon derived from the leaves of common polypody (Polypodium vulgare) via chemical activation with phosphoric acid (H3PO4) at activation temperatures of 700, 800, and 900 °C. An unconventional approach to porous structure analysis, using the new numerical clustering-based adsorption analysis (LBET) method together with the implemented unique gas state equation, was used in this study. The LBET method is based on unique mathematical models that take into account, in addition to surface heterogeneity, the possibility of molecule clusters branching and the geometric and energy limitations of adsorbate cluster formation. It enabled us to determine a set of parameters comprehensively and reliably describing the porous structure of carbon material on the basis of the determined adsorption isotherm. Porous structure analyses using the LBET method were based on nitrogen (N2), carbon dioxide (CO2), and methane (CH4) adsorption isotherms determined for individual activated carbon. The analyses carried out showed the highest CO2 adsorption capacity for activated carbon obtained was at an activation temperature of 900 °C, a value only slightly higher than that obtained for activated carbon prepared at 700 °C, but the values of geometrical parameters determined for these activated carbons showed significant differences. The results of the analyses obtained with the LBET method were also compared with the results of iodine number analysis and the results obtained with the Brunauer–Emmett–Teller (BET), Dubinin–Radushkevich (DR), and quenched solid density functional theory (QSDFT) methods, demonstrating their complementarity.


2013 ◽  
Vol 16 (1) ◽  
pp. 22-31
Author(s):  
Phung Thi Kim Le ◽  
Kien Anh Le

Agricultural wastes are considered to be a very important feedstock for activated carbon production as they are renewable sources and low cost materials. This study present the optimize conditions for preparation of durian peel activated carbon (DPAC) for removal of methylene blue (MB) from synthetic effluents. The effects of carbonization temperature (from 673K to 923K) and impregnation ratio (from 0.2 to 1.0) with potassium hydroxide KOH on the yield, surface area and the dye adsorbed capacity of the activated carbons were investigated. The dye removal capacity was evaluated with methylene blue. In comparison with the commercial grade carbons, the activated carbons from durian peel showed considerably higher surface area especially in the suitable temperate and impregnation ratio of activated carbon production. Methylene blue removal capacity appeared to be comparable to commercial products; it shows the potential of durian peel as a biomass source to produce adsorbents for waste water treatment and other application. Optimize condition for preparation of DPAC determined by using response surface methodology was at temperature 760 K and IR 1.0 which resulted the yield (51%), surface area (786 m2/g), and MB removal (172 mg/g).


Energies ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2237
Author(s):  
Sara Stelitano ◽  
Giuseppe Conte ◽  
Alfonso Policicchio ◽  
Alfredo Aloise ◽  
Giovanni Desiderio ◽  
...  

Pinecones, a common biomass waste, has an interesting composition in terms of cellulose and lignine content that makes them excellent precursors in various activated carbon production processes. The synthesized, nanostructured, activated carbon materials show textural properties, a high specific surface area, and a large volume of micropores, which are all features that make them suitable for various applications ranging from the purification of water to energy storage. Amongst them, a very interesting application is hydrogen storage. For this purpose, activated carbon from pinecones were prepared using chemical activation with different KOH/precursor ratios, and their hydrogen adsorption capacity was evaluated at liquid nitrogen temperatures (77 K) at pressures of up to 80 bar using a Sievert’s type volumetric apparatus. Regarding the comprehensive characterization of the samples’ textural properties, the measurement of the surface area was carried out using the Brunauer–Emmett–Teller method, the chemical composition was investigated using wavelength-dispersive spectrometry, and the topography and long-range order was estimated using scanning electron microscopy and X-ray diffraction, respectively. The hydrogen adsorption properties of the activated carbon samples were measured and then fitted using the Langmuir/ Töth isotherm model to estimate the adsorption capacity at higher pressures. The results showed that chemical activation induced the formation of an optimal pore size distribution for hydrogen adsorption centered at about 0.5 nm and the proportion of micropore volume was higher than 50%, which resulted in an adsorption capacity of 5.5 wt% at 77 K and 80 bar; this was an increase of as much as 150% relative to the one predicted by the Chahine rule.


2019 ◽  
Vol 9 (7) ◽  
pp. 1371 ◽  
Author(s):  
Stefano Cimino ◽  
Jessica Apuzzo ◽  
Luciana Lisi

MgO supported on activated carbon (AC) with a load ranging from 10% to 30% has been investigated as catalyst for the conversion of ethanol into butanol at 400 °C in a fixed bed reactor at different GHSV. Catalysts have been characterized by XRD, SEM/EDX, and N2 physisorption at 77 K. The high dispersion of MgO into the pores of the support provides strongly enhanced performance with respect to bulk MgO. MgO/AC catalysts have been also tested under wet feed conditions showing high water tolerance and significantly larger butanol yield with respect to an alumina supported Ru/MgO catalyst. After wet operation, the increased surface area of the catalyst leads to better performance once dry feed conditions are restored.


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