Synthesis and Characterization of Mg(OH)2-Impregnated Activated Carbon Adsorbent from Coconut Shell

2019 ◽  
Vol 948 ◽  
pp. 49-53
Author(s):  
Andri Saputra ◽  
Hary Sulistyo ◽  
Deni Swantomo

Introducing or impregnating Mg(OH)2onto activated carbon is a promising path for wastewater treatment of uptake (removal) uranium from aqueous solution. The present study aims to synthesize and characterize Mg(OH)­2-impregnated activated carbon from coconut shell. The introducing or impregnating Mg(OH)2into treated biochar by activation method using various impregnation ratio (IR) of MgCl2(IR = 0.5; 1.0; 2.0). Characterization of functional groups in produced activated carbon was conducted with the aid of FTIR spectroscopy. The presence of O-H or Mg(hydroxyl) bond was confirmed by FTIR analysis at 3343.50 cm-1with the highest intensity of the obtained peak at impregnation ratio (IR) 2.0. Due to the surface area is one of the important factors that control a material’s ability to adsorb contaminations, the surface area of activated carbon was measured about 353-358 m2/g by BET method. To indicate that introducing or impregnating Mg(OH)2or Mg(hydroxyl) into treated carbon is successfully work, the presence of Mg (%w) in activated carbon was performed using X-Ray Fluorescence Analysis with the highest Mg presence about 28.587 (%w) at impregnation ratio (IR) 2.0.

2016 ◽  
Vol 835 ◽  
pp. 289-298 ◽  
Author(s):  
M.I.M. Nayai ◽  
Khudzir Ismail ◽  
Mohd Azlan Mohd Ishak ◽  
N. Zaharudin ◽  
Wan Izhan Nawawi

Coconut shell-based activated carbon (CSAc) was prepared by chemical activation method using microwave-induced KOH technique. The activation process was successfully carried out with varying microwave power ranging from 100 to 1000 W and impregnation ratio of 1.0 to 3.0. The surface area, pore sizes, surface morphology and specific capacitance of the produced activated carbon were analyzed by using an automatic quantachrome instrument (Autosorb1C) volumetric sorption analyzer, scanning electron microscope (SEM) and automatic battery cycler. The optimum activation power and impregnation ratio were found at 600 W and 1.5, respectively. The resulted product, C3 has maximum surface area and specific capacitance value of 1768.8 m2 g-1 and 156.33 F g-1 respectively, with carbon yield of 58 %.


2015 ◽  
Vol 11 (1) ◽  
pp. 47
Author(s):  
Hartini Hartini ◽  
Yuniawan Hidayat ◽  
Mudjijono Mudjijono

<p>A composite of γ-alumina and activated carbon made of cassava peels was studied in terms of its pore structures and its properties. The objective of this study was to determine the interaction and structure, as well as the character and pore size of γ-alumina – activated carbon composite.</p><p>Carbon made of cassava peels was activated by H<sub>2</sub>SO<sub>4</sub> and its activities were tested according to the Indonesian Industrial Standards (SII). The addition of activated carbon into γ-alumina made in variations of 10, 20, 30, 40 and 50 % w/w, of the total weight of 10 grams. The composite of γ-alumina - activated carbon was characterized by FTIR, SAA (Surface Area Analyzer), XRD, and determination of Hysteresis Loop composites.</p>The greater addition of activated carbon to γ-alumina causes intermolecular interactions between –O-H groups form rehydrated hydrogen bonds in the composite is greater. The structure of γ-alumina in the composites remain intact although the percentage of activated carbon in composite is large. The total pore volume and surface area using the BET method of the composite decreases with increasing activated carbon percentage. The greater addition of activated carbon to γ-alumina causes size of mesoporous composites decreased with the characteristic of a composite formed is closer to the activated carbon.


2016 ◽  
Vol 11 (1) ◽  
pp. 47
Author(s):  
Hartini Hartini ◽  
Yuniawan Hidayat ◽  
Mudjijono Mudjijono

<p>A composite of γ-alumina and activated carbon made of cassava peels was studied in terms of its pore structures and its properties. The objective of this study was to determine the interaction and structure, as well as the character and pore size of γ-alumina – activated carbon composite.</p><p>Carbon made of cassava peels was activated by H<sub>2</sub>SO<sub>4</sub> and its activities were tested according to the Indonesian Industrial Standards (SII). The addition of activated carbon into γ-alumina made in variations of 10, 20, 30, 40 and 50 % w/w, of the total weight of 10 grams. The composite of γ-alumina - activated carbon was characterized by FTIR, SAA (Surface Area Analyzer), XRD, and determination of Hysteresis Loop composites.</p>The greater addition of activated carbon to γ-alumina causes intermolecular interactions between –O-H groups form rehydrated hydrogen bonds in the composite is greater. The structure of γ-alumina in the composites remain intact although the percentage of activated carbon in composite is large. The total pore volume and surface area using the BET method of the composite decreases with increasing activated carbon percentage. The greater addition of activated carbon to γ-alumina causes size of mesoporous composites decreased with the characteristic of a composite formed is closer to the activated carbon.


2020 ◽  
Vol 20 (1) ◽  
pp. 44-50
Author(s):  
Cucun Alep Riyanto ◽  
Muhamad Syaiful Ampri ◽  
Yohanes Martono

Nano activated carbon is activated carbon with nano-sized carbon particles and can be synthesized from cellulose-containing materials such as the Annatto peels. In this study, the synthesis of nano activated carbon of the Annatto peels was carried out in terms of activation temperature variations and the carbon impregnation ratio of 50% H3PO4 acid and determining the characteristics of nano activated carbon from Annatto peels (NAPAC). The activation method used is the impregnation of carbon in 50% H3PO4 with a ratio of 1: 3; 1: 4; 1: 5; 1: 6; and 1: 7 (w/w) for 24 hours and heating at 400; 500; 600; 700; and 800 °C for one hour. Nano activated carbon from Annatto peels (NAPAC) was characterized by Infrared Spectrophotometer (FTIR), X-ray Diffractometer (XRD), and Transmission Electron Microscope (TEM). The results of the study showed that the NAPAC can be synthesized from Annatto peels with activation by 50% H3PO4 at the temperature of 500°C and the impregnation ratio of 1:5 (w/w). 


2016 ◽  
Vol 1133 ◽  
pp. 547-551 ◽  
Author(s):  
Ali E.I. Elkhalifah ◽  
Mohammad Azmi Bustam ◽  
Azmi Mohd Shariff ◽  
Sami Ullah ◽  
Nadia Riaz ◽  
...  

The present work aims at a better understanding of the influences of the intercalated mono-, di- and triethanolamines on the characteristics and CO2 adsorption ability of sodium form of bentonite (Na-bentonite). The results revealed that the molar mass of intercalated amines significantly influenced the structural and surface properties as well as the CO2 adsorption capacity of Na-bentonite. In this respect, a stepwise increase in the d-spacing of Na-bentonite with the molar mass of amine was recorded by XRD technique. However, an inverse effect of the molar mass of amine on the surface area was confirmed by BET method. CO2 adsorption experiments on amine-bentonite hybrid adsorbents showed that the CO2 adsorption capacity inversly related to the molar mass of amine at 25 ͦC and 101 kPa. Accordingly, Na-bentonite modified by monoethanolammonium cations adsorbed as high as 0.475 mmol CO2/g compared to 0.148 and 0.087 mmol CO2/g for that one treated with di- and triethanolammonium cations, respectively.


Processes ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 217
Author(s):  
Marin Ugrina ◽  
Martin Gaberšek ◽  
Aleksandra Daković ◽  
Ivona Nuić

Sulfur-impregnated zeolite has been obtained from the natural zeolite clinoptilolite by chemical modification with Na2S at 150 °C. The purpose of zeolite impregnation was to enhance the sorption of Hg(II) from aqueous solutions. Chemical analysis, acid and basic properties determined by Bohem’s method, chemical behavior at different pHo values, zeta potential, cation-exchange capacity (CEC), specific surface area, X-ray powder diffraction (XRPD), scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), as well as thermogravimetry with derivative thermogravimetry (TG-DTG) were used for detailed comparative mineralogical and physico-chemical characterization of natural and sulfur-impregnated zeolites. Results revealed that the surface of the natural zeolite was successfully impregnated with sulfur species in the form of FeS and CaS. Chemical modification caused an increase in basicity and the net negative surface charge due to an increase in oxygen-containing functional groups as well as a decrease in specific surface area and crystallinity due to the formation of sulfur-containing clusters at the zeolite surface. The sorption of Hg(II) species onto the sulfur-impregnated zeolite was affected by the pH, solid/liquid ratio, initial Hg(II) concentration, and contact time. The optimal sorption conditions were determined as pH 2, a solid/liquid ratio of 10 g/L, and a contact time of 800 min. The maximum obtained sorption capacity of the sulfur-impregnated zeolite toward Hg(II) was 1.02 mmol/g. The sorption mechanism of Hg(II) onto the sulfur-impregnated zeolite involves electrostatic attraction, ion exchange, and surface complexation, accompanied by co-precipitation of Hg(II) in the form of HgS. It was found that sulfur-impregnation enhanced the sorption of Hg(II) by 3.6 times compared to the natural zeolite. The leaching test indicated the retention of Hg(II) in the zeolite structure over a wide pH range, making this sulfur-impregnated sorbent a promising material for the remediation of a mercury-polluted environment.


2015 ◽  
Vol 212 (3) ◽  
pp. 523-528 ◽  
Author(s):  
Philipp Hönicke ◽  
Blanka Detlefs ◽  
Matthias Müller ◽  
Erik Darlatt ◽  
Emmanuel Nolot ◽  
...  

2013 ◽  
Vol 594-595 ◽  
pp. 73-77 ◽  
Author(s):  
Sze Mei Chin ◽  
Suriati Sufian ◽  
Jeefferie Abd Razak

This paper highlights on the hydrogen production through photocatalytic activity by using hematite nanoparticles synthesized from self-combustion method based on different stirring period. The morphologies and microstructures of the nanostructures were determined using Field-Emission Scanning Electron Microscope (FESEM), X-Ray Diffractometer (XRD) and Particle Size Analyser (PSA). Besides that, surface area analyser was used to determine the BET surface area of the hematite samples. The hematite nanocatalyst as-synthesized are proven to be rhombohedral crystalline hematite (α-Fe2O3) with particle diameters ranging from 60-140 nm. The BET specific surface area of hematite samples increased from 5.437 to 7.6425 m2/g with increasing stirring period from 1 to 4 weeks. This caused the amount of hydrogen gas produced from photocatalytic water splitting to increase as well.


2007 ◽  
Vol 336-338 ◽  
pp. 1914-1917
Author(s):  
Lei Yang ◽  
Zhen Yi Zhang ◽  
Xiao Shan Ning ◽  
Guang He Li

In this paper, a novel and highly efficient hydroxyapatite (HA) carrier for cultivating hydrocarbon degradation bacteria (HDB) is introduced. The HA particles synthesized through a sol-gel method and different heat treatments were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and BET method. The microbial amount and activities of HDB cultivated on HA carriers were quantitatively investigated in order to assess their enriching capabilities. The results showed that HA synthesized at 550°C and the one without calcination could enrich HDB 3 and 2 magnitude orders more than the activated carbon, respectively. Mechanisms of bacterial enrichment on HA and activated carbon were also studied, and it is believed that the high bioactivity and the surface morphology of HA were responsible for the efficient reproduction of HDB. It is concluded that HA is a potential candidate to replace the conventionally used activated carbon as a novel carrier applied in the filed of bioremediation for oil contaminated soil.


2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Esmael Salimi ◽  
Jafar Javadpour

Wormhole-like mesostructured monetite was successfully synthesized using cetyltrimethylammonium bromide (C19H42BrN, CTAB), as a porosity agent. X-ray techniques and FTIR reveal that the crystalline grains consist of highly crystalline pure monetite phase. Monetite rods with diameter around 20–40 nm and length in the range of 50–200 nm were confirmed by FESEM and TEM. Based on N2adsorption-desorption isotherms investigation, surface area increased up to 31.5 m2/g due to the removal of surfactant after calcinations at 400°C. The results indicate that CTAB can not only affect monetite crystallization but also change particles morphology from plate shape to rod-like.


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