scholarly journals Potential Use of Waste Activated Sludge Hydrothermally Treated as a Renewable Fuel or Activated Carbon Precursor

Molecules ◽  
2020 ◽  
Vol 25 (15) ◽  
pp. 3534
Author(s):  
J. A. Villamil ◽  
E. Diaz ◽  
M. A. de la Rubia ◽  
A. F. Mohedano

In this work, dewatered waste activated sludge (DWAS) was subjected to hydrothermal carbonization to obtain hydrochars that can be used as renewable solid fuels or activated carbon precursors. A central composite rotatable design was used to analyze the effect of temperature (140–220 °C) and reaction time (0.5–4 h) on the physicochemical properties of the products. The hydrochars exhibited increased heating values (up to 22.3 MJ/kg) and their air-activation provided carbons with a low BET area (100 m2/g). By contrast, chemical activation with K2CO3, KOH, FeCl3 and ZnCl2 gave carbons with a well-developed porous network (BET areas of 410–1030 m2/g) and substantial contents in mesopores (0.079–0.271 cm3/g) and micropores (0.136–0.398 cm3/g). The chemically activated carbons had a fairly good potential to adsorb emerging pollutants such as sulfamethoxazole, antipyrine and desipramine from the liquid phase. This was especially the case with KOH-activated hydrochars, which exhibited a maximum adsorption capacity of 412, 198 and 146 mg/g, respectively, for the previous pollutants.

2019 ◽  
Author(s):  
Chem Int

Activated carbon was prepared from molasses, which are natural precursors of vegetable origin resulting from the sugar industry. A simple elaboration process, based on chemical activation with phosphoric acid, was proposed. The final product, prepared by activation of molasses/phosphoric acid mixture in air at 500°C, presented high surface area (more than 1400 m2/g) and important maximum adsorption capacity for methylene blue (625 mg/g) and iodine (1660 mg/g). The activated carbon (MP2(500)) showed a good potential for the adsorption of Cr(VI), Cu(II) and Pb(II) from aqueous solutions. The affinity for the three ions was observed in the following order Cu2+ Cr6+ Pb2+. The process is governed by monolayer adsorption following the Langmuir model, with a correlation coefficient close to unity.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
N. Mojoudi ◽  
N. Mirghaffari ◽  
M. Soleimani ◽  
H. Shariatmadari ◽  
C. Belver ◽  
...  

AbstractThe purpose of this study was the preparation, characterization and application of high-performance activated carbons (ACs) derived from oily sludge through chemical activation by KOH. The produced ACs were characterized using iodine number, N2 adsorption-desorption, Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The activated carbon prepared under optimum conditions showed a predominantly microporous structure with a BET surface area of 2263 m2 g−1, a total pore volume of 1.37 cm3 g−1 and a micro pore volume of 1.004 cm3 g−1. The kinetics and equilibrium adsorption data of phenol fitted well to the pseudo second order model (R2 = 0.99) and Freundlich isotherm (R2 = 0.99), respectively. The maximum adsorption capacity based on the Langmuir model (434 mg g−1) with a relatively fast adsorption rate (equilibrium time of 30 min) was achieved under an optimum pH value of 6.0. Thermodynamic parameters were negative and showed that adsorption of phenol onto the activated carbon was feasible, spontaneous and exothermic. Desorption of phenol from the adsorbent using 0.1 M NaOH was about 87.8% in the first adsorption/desorption cycle and did not decrease significantly after three cycles. Overall, the synthesized activated carbon from oily sludge could be a promising adsorbent for the removal of phenol from polluted water.


2009 ◽  
Vol 59 (12) ◽  
pp. 2387-2394 ◽  
Author(s):  
X. Wang ◽  
N. Zhu ◽  
J. Xu ◽  
B. Yin

An improved method for preparing activated carbons from wet waste activated sludge (WAS) by direct chemical activation was studied in this paper. The effects of processing parameters on iodine adsorption capacity of the product were investigated. Results show that sludge-based activated carbon prepared with KOH had a larger iodine value than those activated with ZnCl2 and KCl. The maximum iodine value was observed at the KOH concentration of 0.50 M. Increasing the impregnation time from 10 to 20 h resulted in a 20% increase in the iodine value. The highest iodine value was obtained at the activation temperature of 600°C and holding time of 1 h. Sludge water content had insignificant effects on the iodine value of products. Raw WAS with a water content of 93.2% can be converted into an activated carbon with a high specific surface area of 737.6 m2 g−1 and iodine value of 864.8 mgg−1 under optimum experimental conditions. Other physical properties such as total pore volume, micropore volume and mean pore diameter of the product were also reported and compared with those of commercial activated carbon.


Metalurgi ◽  
2021 ◽  
Vol 36 (2) ◽  
Author(s):  
Yohana Fransiska Ferawati ◽  
Ratna Frida Susanti

This work studied the effect of nitrogen functional group modification on activated carbon synthesized from vetiver root waste on pores development. Synthesis of activated carbon was carried out by hydrothermal carbonization of vetiver root waste at a temperature of 225 ⁰C for 18 hours followed by chemical activation using K2FeO4as activated agent in a furnace at temperature of 800 ⁰C for 2 hours with nitrogen atmosphere flowed at a rate of 100 mL/minute. Urea was used as a nitrogen source. The variation of urea concentration was 1:0 (AC0–800), 1:3 (AC3–800) and 1:5 (AC5–800). The results showed that these activated carbons have mesoporous characteristics with the largest Brunauer Emmett Teller (SBET) surface area of 552.90 m2g-1 and average pore width 3,43 nm. The presence of nitrogen functional group was observed in the Fourier Transform Infrared Spectrometer analysis. Synthesis of activated carbon from vetiver root waste with an addition of urea is the newest method to produce mesoporous activated carbon for electrode and  support catalyst purposes.


2020 ◽  
Vol 38 (5-6) ◽  
pp. 191-204
Author(s):  
AL Paredes-Doig ◽  
A Pinedo-Flores ◽  
J Aylas-Orejón ◽  
D Obregón-Valencia ◽  
MR Sun Kou

Activated carbon was prepared from the seeds of aguaje palm ( Mauritia flexuosa L.f.) by a chemical activation with phosphoric acid. This activated carbon was used for adsorbing metal ions: Pb(II), Cd(II), and Cr(III). To understand the mechanism of adsorption of these heavy metals (Cr, Cd, and Pb), the activated carbon surface was oxidized with nitric acid (1 M) increasing the oxygenated surface groups showing an increasing in their adsorption capacities of these metals. The oxidized activated carbon slightly increased the maximum adsorption capacity to 5–7%. The order of adsorption for unoxidized and oxidized activated carbons was Pb> Cd> Cr. This experimental information was corroborated by molecular modeling program Hyperchem 8 based adsorption mainly on two factors: the electron density and orbitals—highest occupied molecular orbital and lowest unoccupied molecular orbital.Activated carbons were characterized by adsorption/desorption of N2, obtaining an increase of microporous surface area for oxidized activated carbon. An increase of surface acidity and a reduction of isoelectric points were observed in oxidized activated carbon. According to these results, the adsorption of metal ions is favored in contact with an oxidized activated carbon, which has more amount of phenolic and carboxylic functional groups. Similarly, decreasing the isoelectric point indicates that the surface has a higher negative charge. The surface information was corroborated by Hyperchem, which indicates that the surface of the oxidized activated carbon has a higher electron density, indicating a larger amount of electrons on its surface, which means the surface of oxidized activated carbon charges negatively and thereby attracts metal ions.


Water ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 1164 ◽  
Author(s):  
Anh Tuan Vo ◽  
Van Phuong Nguyen ◽  
Abdelkader Ouakouak ◽  
Aileen Nieva ◽  
Bonifacio T. Doma ◽  
...  

Three carbonaceous porous materials (biochar and activated carbon) were developed from the Tectona grandis tree sawdust. The applied process of two-stage preparation included pre-treatment through hydrothermal carbonization at 190 °C and subsequent pyrolysis at 800 °C. Two chemical activating agents (K2CO3 and ZnCl2) were used to prepared activated carbons (K2CO3-AC and ZnCl2-AC), respectively. They were characterized by textural property, morphology, and surface element components and applied to remove Cr(VI) from solution at various solution pH values and initial Cr(VI) concentrations. Results showed that the textural parameters (SBET and VTotal) of the prepared material were 1757 m2/g and 1.027 cm3/g for Zn-Cl2-AC, 1013 m2/g and 0.418 cm3/g for K2CO3-AC, and 792 m2/g and 0.345 cm3/g for biochar. The adsorption process reached the highest efficiency at pH 3.0. The Langmuir maximum adsorption capacity indicated the decreasing order: ZnCl2-AC (127 mg/g) > K2CO3-AC (103 mg/g) > biochar (83.5 mg/g). The removal mechanism of Cr(V) from solution was regarded as an adsorption-coupled reduction, namely (1) partial reduction of Cr(VI) into Cr(III) during the adsorption process and (2) adsorption of the Cr(VI) anions through electrostatic attraction and pore filling and the reduced Cr(III) cations through complexation, Cπ–cation interaction, cation exchange, and pore filing. Therefore, the prepared biochar and activated carbon can server as promising adsorbents to efficiently remove both Cr(VI) and Cr(III) from water.


2021 ◽  
Vol 22 (2) ◽  
pp. 31-49
Author(s):  
Radhia Nedjai ◽  
Ma’an Fahmi Rashid Alkhatib ◽  
Md Zahangir Alam ◽  
Nassereldeen Ahmed Kabbashi

This article provides results of the usability of baobab fruit shell to produce activated carbons by chemical activation using ZnCl2, H3PO4, and KOH. This study indicated that activated carbon produced from baobab fruit shell fruit can be used as a promising adsorbent for the removal of methylene blue from aqueous solutions. Significant changes on the material surface following the activation process were observed through SEM and FTIR analyses. Scanning electron micrographs of BFS-ACs showed that porous structures were formed during activation, while the FTIR results indicated that the carbons have abundant functional groups on the surface. KOH activation led an activated carbon with a high methylene blue adsorption of 95.54% and maximum adsorption capacity of 113.63 mg/g, which is directly related to the specific surface area of activated carbons. The adsorption isotherm data were fitted to Langmuir and Freundlich adsorption models. The Langmuir isotherm model showed better fit to the equilibrium data than the Freundlich model. The adsorption process was well described by the pseudo-second-order kinetics. The BFS-ACs is an effective and low-cost adsorbent for the removal of MB from an aqueous solution. ABSTRAK: Kajian ini memberi input tentang kebolehgunaan kulit buah baobab bagi menghasilkan karbon teraktifan melalui aktiviti kimia menggunakan ZnCl2, H3PO4, dan KOH. Karbon aktif daripada kulit buah Baobab ini berpotensi sebagai penyerap bagi menyingkir larutan akueus metilin biru. Perubahan ketara pada permukaan bahan diikuti dengan proses pengaktifan dipantau melalui analisis SEM dan FTIR. Imbasan elektron mikrograf BFS-AC menunjukkan struktur porus terhasil semasa proses pengaktifan. Sementara dapatan FTIR menunjukkan karbon mempunyai banyak kumpulan berfungsi pada permukaan. Pengaktifan KOH menghasilkan karbon aktif menggunakan larutan biru metilin yang tinggi sebanyak 95.54% dan kapasiti maksimum penyerapan 113.63 mg/g, iaitu berkadar langsung dengan tumpuan kawasan permukaan karbon aktif berkaitan. Data isoterma penyerapan dibina pada model penyerapan Langmuir dan Freundlich. Model isoterma Langmuir lebih padan pada data keseimbangan berbanding model Freundlich. Proses penyerapan menunjukkan lebih kinetik order-kedua-pseudo. BFS-AC sangat efektif dan penyerap murah bagi membuang MB daripada larutan akues.


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.


2012 ◽  
Vol 1 (3) ◽  
pp. 75 ◽  
Author(s):  
W.D.P Rengga ◽  
M. Sudibandriyo ◽  
M Nasikin

Gas storage is a technology developed with an adsorptive storage method, in which gases are stored as adsorbed components on the certain adsorbent. Formaldehyde is one of the major indoor gaseous pollutants. Depending on its concentration, formaldehyde may cause minor disorder symptoms to a serious injury. Some of the successful applications of technology for the removal of formaldehyde have been reported. However, this paper presents an overview of several studies on the elimination of formaldehyde that has been done by adsorption method because of its simplicity. The adsorption method does not require high energy and the adsorbent used can be obtained from inexpensive materials. Most researchers used activated carbon as an adsorbent for removal of formaldehyde because of its high adsorption capacity. Activated carbons can be produced from many materials such as coals, woods, or agricultural waste. Some of them were prepared by specific activation methods to improve the surface area. Some researchers also used modified activated carbon by adding specific additive to improve its performance in attracting formaldehyde molecules. Proposed modification methods on activation and additive impregnated carbon are thus discussed in this paper for future development and improvement of formaldehyde adsorption on activated carbon. Specifically, a waste agricultural product is chosen for activated carbon raw material because it is renewable and gives an added value to the materials. The study indicates that the performance of the adsorption of formaldehyde might be improved by using modified activated carbon. Bamboo seems to be the most appropriate raw materials to produce activated carbon combined with applying chemical activation method and addition of metal oxidative catalysts such as Cu or Ag in nano size particles. Bamboo activated carbon can be developed in addition to the capture of formaldehyde as well as the storage of adsorptive hydrogen gas that supports renewable energy. Keywords: adsorption; bamboo; formaldehyde; modified activated carbon; nano size particles


2015 ◽  
Vol 74 (11) ◽  
Author(s):  
Riry Wirasnita ◽  
Tony Hadibarata ◽  
Abdull Rahim Mohd Yusoff ◽  
Zainab Mat Lazim

An oil palm empty fruit bunch-derived activated carbon has been successfully produced by chemical activation with zinc chloride and without chemical activation. The preparation was conducted in the tube furnace at 500oC for 1 h. The surface structure and active sites of activated carbons were characterized by means of Fourier transform infrared spectrometry and field emission scanning electron microscopy. The proximate analysis including moisture content, ash content, bulk density, pH, and pH at zero charge was conducted to identify the psychochemical properties of the adsorbent. The results showed that the zinc chloride-activated carbon has better characteristics compared to the carbon without chemical activation.  


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