Characteristics of Potassium Acetate - Activated Coconut Shell Carbon

2014 ◽  
Vol 1043 ◽  
pp. 193-197
Author(s):  
Noor Shawal Nasri ◽  
Jibril Mohammed ◽  
Muhammad Abbas Ahmad Zaini ◽  
Usman Dadum Hamza ◽  
Husna Mohd. Zain ◽  
...  

There is significant portion of agricultural wastes in the world posing environmental challenge; however, they could be converted into useful products like activated carbon. In this study, coconut shell based carbons were synthesized using chemical activation with potassium acetate (PAAC), potassium hydroxide (PHAC) and physical activation by CO2 (CSAC). The properties of potassium acetate-activated carbon were characterized and the results were compared with the other activation methods. The pyrolysis temperature of 700°C for 2h yielded 32% of char. The BET surface area and pore volume of PAAC are 622m2/g and 0.31cm3/g; while 369m2/g and 0.19cm3/g, and 1354m2/g and 0.61cm3/g were recorded for CSAC and PHAC, respectively. CSAC yielded lower surface area with approximately 88% micropores. On the other hand, PAAC yielded higher surface area with approximately 50% of both micropores and mesopores, whereby this heteroporous property would suffice for a wider range of application. From the Fourier Transform Infrared Spectroscopy analysis, hydroxyls, alkenes, carbonyls and aromatics functional groups were identified with more prominent peaks on the chemically activated porous carbons. From thermogravimetric analysis (TGA), lignin decomposition occurred in a wider temperature range (390-650°C). The properties of PAAC could offer a sustainable means for treatment of toxic waste streams.

2014 ◽  
Vol 554 ◽  
pp. 22-26 ◽  
Author(s):  
Jibril Mohammed ◽  
Noor Shawal Nasri ◽  
Muhammad Abbas Ahmad Zaini ◽  
Usman Hamza Dadum ◽  
Murtala Musa Ahmed

There is significantly abundant portion of waste agricultural materials in the world serving as environmental challenge, however, they could be converted into useful value added products like activated carbon. Coconut shell based carbons were synthesized using physical activation by CO2 and chemical activation with potassium hydroxide and potassium acetate. The BET surface areas and pore volumes are 361m2/g and 0.19cm3/g for physical activation, 1353m2/g and 0.61cm3/g for activation with KOH and 622m2/g and 0.31cm3/g for potassium acetate activated carbon. From the Fourier Transform Infrared Spectroscopy analysis, hydroxyls, alkenes and carbonyl functional groups were identified with more prominence on the chemically activated porous carbons. Thermogravimetric analysis (TGA) results showed occurrence of moisture pyrolysis at 105°C, the pyrolysis of hemicellulose and cellulose occurred at 160–390°C and lignin at (390-650°C). Carbonization at 700°C and 2hrs had highest yield of 32%. Physical activation yielded lower surface area with approximately 88% micropores. On the other hand, chemically activation yielded higher surface area with elevated mesopores. The porous carbons can be applied to salvage pollution challenges.


2014 ◽  
Vol 875-877 ◽  
pp. 1585-1589
Author(s):  
Arenst Andreas Arie ◽  
Joong Kee Lee

Activated carbons were prepared from coconut shell by chemical activation method and utilized as electrode materials for electrochemical double layer capacitor (EDLC). A preliminary characteristic of activated carbon from coconut shell includes the Brunnaeur Emmett Teller (BET) analysis and cyclic voltammetry measurements. The BET surface area is not affected by the variation of activation temperature as both of the samples showed BET surface area of about 850-870 m2g-1. The N2 adsorption–desorption isotherms showed that the sample exhibited type I characteristics according to IUPAC classification, which confirms its micro-porosity. Compared with the un-activated carbon samples, the activated ones exhibited the better electrochemical properties with a specific capacitance of 150 F g−1 at a scan rate of 2 mV s−1. The good performance of activated carbon is attributed to the enhancement of surface area due to the KOH pretreatment which can open new pores accessible for the ionic transport


2014 ◽  
Vol 14 (1) ◽  
pp. 82-98
Author(s):  
Andy Mizwar

Limbah rotan dari industri kerajinan dan mebel berpotensi untuk dijadikan sebagai bahan baku pembuatan karbon aktif karena memiliki kandungan holoselulosa dan kadar karbon yang tinggi. Penelitian ini bertujuan untuk menganalisis efektifitas dari aktivasi kimia menggunakan larutan natrium klorida (NaCl) yang dilanjutkan dengan aktivasi fisik dalam pembuatan karbon aktif berbahan dasar  limbah serutan rotan. Pembuatan karbon aktif diawali dengan proses karbonisasi pada suhu 250°C selama 1 jam. Selanjutnya aktivasi kimia menggunakan larutan NaCl dengan variasi konsentrasi 10%, 15% dan 20% serta waktu perendaman selama 10, 15 dan 20 jam. Aktivasi fisik dilakukan dengan pembakaran pada suhu 700°C selama 30 menit. Analisis karakteristik fisik-kimia karbon aktif mengacu pada SNI 06-3730-95, meliputi kadar air, fixed carbon, dan iodine number, sedangkan perhitungan luas permukaan spesifik karbon aktif dilakukan dengan Metode Sears. Hasil penelitian ini menunjukkan bahwa kondisi optimum aktivasi kimia terjadi pada konsentrasi NaCl 10% dan lama perendaman 10 jam dengan hasil analisis kadar air 2.90%, fixed carbon 72.70%, iodine number 994.59 mg/g dan luas permukaan 1587.67 m²/g. Peningkatan fixed carbon, iodine number dan luas permukaan karbon aktif berbanding terbalik dengan peningkatan konsentrasi NaCl dan lama waktu perendaman, sedangkan peningkatan kadar air pada karbon aktif berlaku sebaliknya. Rattan waste from handicraft and furniture industry could potentially be used as raw material of activated carbon due to high content of holoselulosa and carbon. This paper investigates the effectiveness of chemical activation using sodium chloride (NaCl) followed by physical activation in the making of activated carbon-based on rattan shavings waste. Preparation of the activated carbon began with the carbonization process at 250°C for 1 hour. Furthermore chemical activation using a variation of NaCl concentrations 10%, 15% and 20% as well as the time of immersion 10, 15 and 20 hours. Physical activation was done by burning at 700°C for 30 minutes. Analysis of the physical and chemical characteristics of the activated carbon was referred to the SNI 06-3730-95, including of moisture content, fixed carbon and iodine number, while the calculation of the specific surface area was done by the Sears’s method. The results of this study showed that the optimum conditions of chemical activation occurred in impregnation by NaCl 10% for 10 hours. The water content, fixed carbon, iodine number and surface area of activated carbon was 2.90%, 72.70%, 994.59 mg/g and 1587.67 m²/g  respectively. The increase values of fixed carbon, iodine number, and surface area was inversely proportional to the increase of NaCl concentration and the length of impregnation time, while the increase of water content applied vice versa.


2014 ◽  
Vol 699 ◽  
pp. 87-92 ◽  
Author(s):  
Abdul Rahim Yacob ◽  
Adlina Azmi ◽  
Mohd Khairul Asyraf Amat Mustajab

The characteristics and quality of activated carbons prepared depending on the chemical and physical properties of the starting materials and the activation method used. In this study, activated carbon prepared using pineapple waste. Three parts of pineapple waste which comprises of peel, crown and leaf were studied. For comparison activated carbon were prepared by both physical and chemical activation respectively. Three types of chemicals were used, phosphoric acid (H3PO4), sulphuric acid (H2SO4), and potassium hydroxide (KOH). The preparation includes carbonization at 200°C and activation at the 400°C using muffle furnace. The chemical characterization of the activated carbon was carried out using Thermogravimetric analysis (TGA), Nitrogen gas adsorption analysis and Fourier transform infrared (FTIR). The highest BET surface area was achieved when the pineapple peel soaked in 20% phosphoric acid with a surface area of 1115 m2g-1. FTIR analysis indicates that the reacted pineapple waste successfully converted into activated carbons.


2018 ◽  
Vol 10 (3) ◽  
pp. 149
Author(s):  
Mahmud Sudibandriyo ◽  
L Lydia

Surface area characterization of activated carbon from sugarcane baggase by chemical activationAdsorption is one the process with many applications in the industries such as in a separation or in gas storage. In this adsorption, adsorbent selection is the most important thing. One of the adsorbent most suitable for this process is activated carbon. Previous studies show that high surface area of activated carbon can be produced from sugarcane bagasse using activator ZnCl2. The research’s goal is to produce activated carbon from sugarcane bagasse and determine the effects of activator on the surface area of activated carbon produced. Activators used in this research are KOH and ZnCl2 with the mass ratio of activator/carbon are 1/1, 2/1 and 3/1. The results show that The highest surface area, 938,2 m2/g, is obtained by activation using KOH with mass ratio of activator/carbon 3/1, whereas the highest surface area by activation using ZnCl2 is 632 m2/g with mass ratio of activator/carbon 2/1. For comparison, preparation of activated carbon by physical activation is also done and the surface area is 293 m2/g.Keywords: Activated carbon, chemical activation, sugarcane bagasse, KOH, ZnCl2 Abstrak Adsorpsi merupakan salah satu proses yang banyak digunakan dalam industri baik dalam pemisahan maupun untuk penyimpanan gas. Pada proses adsorpsi ini, pemilihan adsorben merupakan hal yang sangat penting. Salah satu jenis adsorben yang sangat cocok untuk proses ini adalah karbon aktif. Penelusuran studi sebelumnya menunjukkan bahwa karbon aktif dengan luas permukaan yang cukup tinggi dapat dibuat dari ampas tebu dengan menggunakan aktivator ZnCl2. Penelitian ini bertujuan untuk menghasilkan karbon aktif dari ampas tebu dengan aktivasi kimia serta mengetahui pengaruh aktivator terhadap luas permukaan karbon aktif yang dihasilkan. Aktivator yang digunakan dalam penelitian ini adalah KOH dan ZnCl2 dengan rasio massa aktivator/massa karbon 1/1, 2/1, dan 3/1. Aktivasi dilakukan pada temperatur 700 oC selama 1 jam. Hasil penelitian menunjukkan bahwa luas permukaan tertinggi sebesar 938,2 m2/g diperoleh dengan aktivasi menggunakan KOH dengan rasio massa aktivator/massa arang 3/1, sedangkan aktivasi dengan menggunakan ZnCl2 diperoleh luas permukaan tertinggi sebesar 632 m2/g dengan rasio massa aktivator/massa arang 2/1. Sebagai pembanding, pada penelitian ini juga dilakukan pembuatan karbon aktif dengan metode aktivasi fisika dan diperoleh luas permukaan karbon aktif sebesar 293 m2/g.Kata kunci: Aktivasi kimia, ampas tebu, karbon aktif, KOH, ZnCl2


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.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
S. G. Herawan ◽  
M. S. Hadi ◽  
Md. R. Ayob ◽  
A. Putra

Activated carbons can be produced from different precursors, including coals of different ranks, and lignocellulosic materials, by physical or chemical activation processes. The objective of this paper is to characterize oil-palm shells, as a biomass byproduct from palm-oil mills which were converted into activated carbons by nitrogen pyrolysis followed by CO2activation. The effects of no holding peak pyrolysis temperature on the physical characteristics of the activated carbons are studied. The BET surface area of the activated carbon is investigated using N2adsorption at 77 K with selected temperatures of 500, 600, and 700°C. These pyrolysis conditions for preparing the activated carbons are found to yield higher BET surface area at a pyrolysis temperature of 700°C compared to selected commercial activated carbon. The activated carbons thus result in well-developed porosities and predominantly microporosities. By using this activation method, significant improvement can be obtained in the surface characteristics of the activated carbons. Thus this study shows that the preparation time can be shortened while better results of activated carbon can be produced.


2011 ◽  
Vol 704-705 ◽  
pp. 517-522 ◽  
Author(s):  
Xiao Juan Jin ◽  
Zhi Ming Yu ◽  
Gao Jiang Yan ◽  
Wu Yu

Activated carbons were prepared through chemical activation of lignin from straw pulping precursor using potassium carbonate as the chemical agent. Effects of activated temperature, K2CO3/lignin ratio and the activated time on the yield, Iodine number of activated carbon were investigated. Experimental results indicated that the optimum conditions were as follow: activated temperature 800°C, K3CO3(40% concentration) /lignin ratio 5: l, activated time 50min. These conditions allowed us to obtain a BET surface area of 1104 m2/g, including the external or non-microporous surface of 417 m2/g,Amount of methylene blue adsorption, Iodine number and the yield of activated carbon prepared under optimum conditions were 10.6mL/0.lg,1310 mg/g and 19.75%, respectively.


2015 ◽  
Vol 1113 ◽  
pp. 422-427
Author(s):  
Sethupathi Sumathi ◽  
Wei Liang Chong ◽  
Mohamed J.K. Bashir ◽  
Choon Aun Ng ◽  
Kanthasamy Ramesh

The conversion of sea mango oil into non-edible feedstock for biodiesel will lead to the production of abundant sea mango biomass as waste. Thus in this study, the potential of converting sea mango fiber waste into a value added product was analyzed. Sea mango fiber was utilized to produce activated carbon and was tested on dye removal. The sea mango activated carbon (SMAC) was prepared using physical activation by carbon dioxide. The preparation was carried out by varying the activation temperature (600-900 °C), gas flow rate (50–300 ml/min) and activation time (1.0-2.5 h). The parameters are manipulated using Design of Experiment. The prepared activated carbon was tested on methylene blue dye. SMAC was characterized by SEM, FTIR and BET surface area. Results showed that activation temperature and time have significant effect on the characteristic of SMAC and removal of dye. The optimum conditions for preparing the SMAC having the highest dye removal were found to be activation temperature of 810 °C, 178 ml/min of carbon dioxide flow and 1.9 h of activation time. The results showed that the BET surface area and dye removal efficiency of the SMAC are 540 m2/g and 95.6 % respectively.


2017 ◽  
Vol 4 (2) ◽  
pp. 186-194 ◽  
Author(s):  
Tan I. A. W. ◽  
Abdullah M. O. ◽  
Lim L. L. P. ◽  
Yeo T. H. C.

Activated carbon derived from agricultural biomass has been increasingly recognized as a multifunctional material for various applications according to its physicochemical characteristics. The application of activated carbon in adsorption process mainly depends on the surface chemistry and pore structure which is greatly influenced by the treatment method. This study aims to compare the textural characteristics, surface chemistry and surface morphology of coconut shell-based activated carbon modified using chemical surface treatments with hydrochloric acid (HCl) and sodium hydroxide (NaOH). The untreated and treated activated carbons were characterized for their physical and chemical properties including the Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and textural characterization. The FTIR spectra displayed bands confirming the presence of carboxyl, hydroxyl and carbonyl functional groups. The Brunauer–Emmett–Teller (BET) surface area of the untreated activated carbon was 436 m2/g whereas the surface area of the activated carbon modified using 1M NaOH, 1M HCl and 2M HCl was 346, 525 and 372 m2/g, respectively. SEM micrographs showed that many large pores in a honeycomb shape were clearly found on the surface of 1M HCl sample. The pore structure of the activated carbon treated with 2M HCl and NaOH was partially destroyed or enlarged, which decreased the BET surface area. The modification of the coconut shell-based activated carbon with acidic and alkaline treatments has successfully altered the surface functional groups, surface morphology and textural properties of the activated carbon which could improve its adsorptive selectivity on a certain adsorbate.


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