scholarly journals Highly Selective CO2 Capture on Waste Polyurethane Foam-Based Activated Carbon

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 (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.


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. 


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.


Author(s):  
Nawwarah Mokti ◽  
Azry Borhan ◽  
Siti Nur Azella Zaine ◽  
Hayyiratul Fatimah Mohd Zaid

The use of an activating agent in chemical activation of activated carbon (AC) production is very important as it will help to open the pore structure of AC as adsorbents and could enhance its performance for adsorption capacity. In this study, a pyridinium-based ionic liquid (IL), 1-butylpyridinium bis(trifluoromethylsulfonyl) imide, [C4Py][Tf2N] has been synthesized by using anion exchange reaction and was characterized using few analyses such as 1H-NMR, 13C-NMR and FTIR. Low-cost AC was synthesized by chemical activation process in which rubber seed shell (RSS) and ionic liquid [C4Py][Tf2N] were employed as the precursor and activating agent, respectively. AC has been prepared with different IL concentration (1% and 10%) at 500°C and 800°C for 2 hours. Sample AC2 shows the highest SBET and VT which are 392.8927 m2/g and 0.2059 cm3/g respectively. The surface morphology of synthesized AC can be clearly seen through FESEM analysis. A high concentration of IL in sample AC10 contributed to blockage of pores by the IL. On the other hand, the performance of synthesized AC for CO2 adsorption capacity also studied by using static volumetric technique at 1 bar and 25°C. Sample AC2 contributed the highest CO2 uptakes which is 50.783 cm3/g. This current work shows that the use of low concentration IL as an activating agent has the potential to produce porous AC, which offers low-cost, green technology as well as promising application towards CO2 capture.


2015 ◽  
Vol 1107 ◽  
pp. 347-352 ◽  
Author(s):  
Collin Glen Joseph ◽  
Duduku Krishniah ◽  
Yun Hin Taufiq-Yap ◽  
Masnah Massuanna ◽  
Jessica William

Abstract. Waste tires, which are an abundant waste product of the automobile industry, were used to prepare activated carbon by means of physical and chemical activation. A two-stage process was used, with a semi-carbonization stage as the first stage, followed by an activation stage as the second stage.All experiments were conducted in a laboratory-scale muffle furnace under static conditions in a self-generated atmosphere. During this process, the effects of the parametric variables of semi-carbonization time (for the physical activation process), activation time and temperature and impregnation ratios (for the chemical activation process) on the percentage yield were studied and compared. Varying these parametric variables yielded interesting results, which in turn affected the adsorption process of 2,4-DCP, which was the simulated pollutant in aqueous form. The optimized percentage yields of activated carbon that were obtained were 41.55% and 44.88% ofthe physical and chemical activation treatment processes respectively.Keywords: Physical activation, chemical activation, waste rubber tires, 2,4-dichlorophenol, activated carbon.


2014 ◽  
Vol 896 ◽  
pp. 179-182 ◽  
Author(s):  
Erman Taer ◽  
Iwantono ◽  
Saidul Tua Manik ◽  
R. Taslim ◽  
D. Dahlan ◽  
...  

Binderless activated carbon monoliths (ACMs) for supercapacitor electrodes were prepared from sugarcane bagasse by two different methods of physical and combination of physical-chemical activation process. The CO2 gas was used as physical activation agent and 0.3 M KOH was chosen as chemical activation agent. The ACMs were tested as electrodes in two-electrode systems of the coin tape cell supercapacitor that consists of stainless steel as current collectors and 1 M H2SO4 as an electrolyte. The improving of resistive, capacitive and energy properties of combination of physical-chemical ACMs electrodes were shown by an impedance spectroscopy, a cyclic voltammetry and a galvanostatic charge-discharge method. The improving of resistive, capacitive and energy properties as high as 1 to 0.6 Ω, 146 to 178 F g-1, 3.83 to 4.72 W h kg-1, respectively. The X-ray diffraction analysis and field emission scanning electron microscope were performed to characterize the crystallite and morphology characteristics. The results showed that the combination of physical-chemical activation process have given a good improving in performance of the bagasse based ACMs electrodes in supercapacitor application.


2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Nurgul Ozbay ◽  
Adife Seyda Yargic

Activated carbons were prepared by carbonization of tomato paste processing industry waste at 500°C followed by chemical activation with KOH, K2CO3, and HCl in N2 atmosphere at low temperature (500°C). The effects of different activating agents and impregnation ratios (25, 50, and 100 wt.%) on the materials’ characteristics were examined. Precursor, carbonized tomato waste (CTW), and activated carbons were characterized by using ultimate and proximate analysis, thermogravimetric analysis (TG/DTG), Fourier transform-infrared (FT-IR) spectroscopy, X-ray fluorescence (XRF) spectroscopy, point of zero charge measurements (pHPZC), particle size analyzer, scanning electron microscopy (SEM), energy dispersive X-ray (EDX) spectroscopy, nitrogen adsorption/desorption isotherms, and X-ray diffraction (XRD) analysis. Activation process improved pore formation and changed activated carbons’ surface characteristics. Activated carbon with the highest surface area (283 m3/g) was prepared by using 50 wt.% KOH as an activator. According to the experimental results, tomato paste waste could be used as an alternative precursor to produce low-cost activated carbon.


Author(s):  
Muhammad S. Muzarpar ◽  
A. M. Leman

Activated carbon (AC) was recognized by many researchers as useful substance in adsorption of impurities. Several processes involved in the production of AC which were carbonization, crushing, and activation process. Carbonization of carbon required high temperature up to 900oC. Then the carbon will be crush to a desired size for activation process. Activation of carbon can be either chemical activation, physical activation or combination of chemical and physical activation which called physiochemical activation. The mechanism adsorption of AC commonly due to its micropore present in the carbon or the weak vander waals forces which can attract the impurities. Activated carbon have multiple function in human daily life. This study will be discuss the function of AC in the production face mask, water filtration and air filtration.


METANA ◽  
2021 ◽  
Vol 17 (2) ◽  
pp. 61-68
Author(s):  
Syarifuddin Oko ◽  
Mustafa Mustafa ◽  
Andri Kurniawan ◽  
Lintang Norfitria

 Pengunaan plastik setiap hari mengakibatkan terjadinya penumpukan sampah plastik yang dapat mencemari lingkungan dan menjadi salah satu masalah serius yang harus ditangani karena plastik tidak dapat terdegradasi. Plastik merupakan senyawa yang unsur penyusun utamanya adalah karbon dan hidrogen. Sehingga limbah plastik berpotensi sebagai pembuatan karbon aktif dan akan membuat limbah plastik menjadi lebih bermanfaat. Penelitian ini bertujuan untuk mengetahui pengaruh konsentrasi aktivator dan waktu aktivasi terhadap proses aktivasi fisika kimia sehingga menghasilkan produk karbon aktif yang sesuai dengan SNI 06-3730-1995. Plastik PET terlebih dahulu dikarbonasi pada temperatur 480oC selama 2 jam menggunakan furnace hingga membentuk arang. Lalu, direndam dalam aseton selama 24 jam. Setelah itu disaring dan dikeringkan menggunakan oven pada temperatur 110oC selama 3 jam dan dilanjutkan dengan proses aktivasi fisika pada temperatur 750oC selama 2 jam. Karbon yang telah teraktivasi fisika selanjutnya diaktivasi secara kimia dengan menggunakan KOH konsentrasi 1 M, 2 M, 3 M, dan 4M dengan variasi waktu  2 jam dan 4 jam. Diperoleh hasil terbaik yaitu pada karbon aktif dengan konsentrasi KOH 4 M dan waktu aktivasi 2 jam dengan nilai daya serap iod sebesar 980,17 mg/g, kadar abu 0,28%, kadar air 7,55%, dan kadar volatile matter 3,47%. Karbon aktif yang diperoleh telah memenuhi SNI 06-3730-1995.The use of plastic every day results in the accumulation of plastic waste that can pollute the environment and was a serious problem that must be addressed because plastic cannot be degraded. Plastic was a compound whose main constituent elements were carbon and hydrogen. So that plastic waste has the potential to produce activated carbon and will make plastic waste more useful. This study aims to determine the effect of activator concentration and activation time on the physical-chemical activation process so as to produce activated carbon products in accordance with SNI 06-3730-1995. PET plastik was first carbonated at a temperature of 480oC for 2 hours using a furnace to form charcoal. Then, soaked in acetone for 24 hours. After that it was filtered and dried using an oven at a temperature of 110oC for 3 hours and continued with the physical activation process at a temperature of 750oC for 2 hours. The physically activated carbon was then chemically activated using KOH concentrations of 1 M, 2 M, 3 M, and 4 M with time variations of 2 hours and 4 hours. The best results were obtained on activated carbon with a concentration of KOH 4 M and an activation time of 2 hours with an iodine absorption value of 980.17 mg/g, 0.28% ash content, 7.55% water content, and volatile matter levels 3,47%. Activated carbon obtained has complied with SNI 06-3730-1995.


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