scholarly journals Mercury removal from modified activated carbon of peat soil and coal in simulated landfill leachate

Author(s):  
Mochammad Arief Budihardjo ◽  
Yudha Gusti Wibowo ◽  
Bimastyaji Surya Ramadan ◽  
Muhamad Allan Serunting ◽  
Eflita Yohana ◽  
...  
Author(s):  
Cong Chen ◽  
Yufeng Duan ◽  
Tianfang Huang ◽  
Mingqing Zhu ◽  
Xiaoshuo Liu ◽  
...  

2018 ◽  
Vol 54 (4) ◽  
pp. 2836-2852 ◽  
Author(s):  
Changming Zhang ◽  
Wen Song ◽  
Xiaochao Zhang ◽  
Rui Li ◽  
Songjian Zhao ◽  
...  

2019 ◽  
Vol 58 (29) ◽  
pp. 13190-13197 ◽  
Author(s):  
Cong Chen ◽  
Yufeng Duan ◽  
Shilin Zhao ◽  
Bin Hu ◽  
Na Li ◽  
...  

Author(s):  
Long Wu ◽  
Zhongsheng Shang ◽  
Hailu Zhu ◽  
Zhanyong Li ◽  
Guangqian Luo ◽  
...  

Abstract During the plasma modification process on activated carbon surface, reactive gas of O2 in the plasma field dominates the formation of oxygen-containing groups on activated carbon surface, which is a key factor that affects the mercury adsorption. Previous studies showed that change the O2 concentration would influence the generation of oxygen-containing groups and thus affect the mercury adsorption. It is important to investigate the effects of O2 concentration in the non-thermal plasma field on the mercury adsorption characteristic of modified activated carbon. This work presents the results of the novel use of non-thermal plasma in Ar-O2 gas to increase surface oxygen functionality on the surface of a commercially available biomass carbon. The volume fraction of O2 in the Ar-O2 mixture was varied from 10 % to 100 %. The surface physical and chemistry properties of modified activated carbon were analyzed by using BET, FT-IR and XPS techniques. Results showed that activated carbon modified by Ar-O2 non-thermal plasma showed significantly better mercury removal performance compared with the original activated carbon. Moreover, increase O2 concentration in the plasma field can further increase the mercury removal efficiency of modified activated carbon. Higher O2 concentration can produce more O radicals during plasma system and facilitated the formation of carbonyl and ester groups on activated carbon surface and thus enhanced the mercury removal. Temperature programmed desorption (TPD) results indicated that mercury reacted with ester groups were prior to carbonyl groups. When O2 concentration increased to 100 %, the ester groups of modified activated carbon dominated the mercury adsorption process.


2017 ◽  
Vol 1 (1) ◽  
pp. 28-30 ◽  
Author(s):  
Azhar Abdul Halim ◽  
Siti Fairuz Abu Sidi ◽  
Marlia M. Hanafiah

2012 ◽  
Vol 11 (8) ◽  
pp. 1433-1438 ◽  
Author(s):  
Jinren Ni ◽  
Guangzhi Zhang ◽  
Hao Hu ◽  
Weiling Sun ◽  
Bin Zhao ◽  
...  

Author(s):  
Zhirui Li ◽  
Yuqi Jin ◽  
Tong Chen ◽  
Feng Tang ◽  
Jie Cai ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 337
Author(s):  
Sara Mesa Medina ◽  
Ana Rey ◽  
Carlos Durán-Valle ◽  
Ana Bahamonde ◽  
Marisol Faraldos

Two commercial activated carbon were functionalized with nitric acid, sulfuric acid, and ethylenediamine to induce the modification of their surface functional groups and facilitate the stability of corresponding AC-supported iron catalysts (Fe/AC-f). Synthetized Fe/AC-f catalysts were characterized to determine bulk and surface composition (elemental analysis, emission spectroscopy, XPS), textural (N2 isotherms), and structural characteristics (XRD). All the Fe/AC-f catalysts were evaluated in the degradation of phenol in ultrapure water matrix by catalytic wet peroxide oxidation (CWPO). Complete pollutant removal at short reaction times (30–60 min) and high TOC reduction (XTOC = 80 % at ≤ 120 min) were always achieved at the conditions tested (500 mg·L−1 catalyst loading, 100 mg·L−1 phenol concentration, stoichiometric H2O2 dose, pH 3, 50 °C and 200 rpm), improving the results found with bare activated carbon supports. The lability of the interactions of iron with functionalized carbon support jeopardizes the stability of some catalysts. This fact could be associated to modifications of the induced surface chemistry after functionalization as a consequence of the iron immobilization procedure. The reusability was demonstrated by four consecutive CWPO cycles where the activity decreased from 1st to 3rd, to become recovered in the 4th run. Fe/AC-f catalysts were applied to treat two real water matrices: the effluent of a wastewater treatment plant with a membrane biological reactor (WWTP-MBR) and a landfill leachate, opening the opportunity to extend the use of these Fe/AC-f catalysts for complex wastewater matrices remediation. The degradation of phenol spiked WWTP-MBR effluent by CWPO using Fe/AC-f catalysts revealed pH of the reaction medium as a critical parameter to obtain complete elimination of the pollutant, only reached at pH 3. On the contrary, significant TOC removal, naturally found in complex landfill leachate, was obtained at natural pH 9 and half stoichiometric H2O2 dose. This highlights the importance of the water matrix in the optimization of the CWPO operating conditions.


Heliyon ◽  
2021 ◽  
pp. e07191
Author(s):  
Fateme Barjasteh-Askari ◽  
Mojtaba Davoudi ◽  
Maryam Dolatabadi ◽  
Saeid Ahmadzadeh

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