scholarly journals Adsorption behaviour and mechanism of the PFOS substitute OBS (sodium p -perfluorous nonenoxybenzene sulfonate) on activated carbon

2019 ◽  
Vol 6 (9) ◽  
pp. 191069 ◽  
Author(s):  
Wei Wang ◽  
Xin Mi ◽  
Huilan Shi ◽  
Xue Zhang ◽  
Ziming Zhou ◽  
...  

Perfluorooctane sulfonate (PFOS) was listed as a persistent organic pollutant by the Stockholm Convention. As a typical alternative to PFOS, sodium p -perfluorous nonenoxybenzene sulfonate (OBS) has recently been detected in the aquatic environment which has caused great concern. For the first time, the adsorption behaviour and mechanism of OBS on activated carbon (AC) with different physical and chemical properties were investigated. Decreasing the particle size of AC can accelerate its adsorption for OBS, while AC with too small particle size was not conducive to its adsorption capacity due to the destruction of its pore structure during the mechanical crushing process. Intra-particle diffusion had a lesser effect on the adsorption rate of AC with smaller particle size, higher hydrophilicity and larger pore size. Reactivation of AC by KOH can greatly enlarge their pore size and surface area, greatly increasing their adsorption capacities. The adsorption capacity of two kinds of R-GAC exceeded 0.35 mmol g −1 , significantly higher than that of other ACs. However, increasing the hydrophilicity of AC would decrease their adsorption capacities. Further investigation indicated that a larger pore size and smaller particle size can greatly enhance the adsorptive removal of OBS on AC in systems with other coexisting PFASs and organic matter due to the reduction of the pore-blocking effect. The spent AC can be successfully regenerated by methanol, and it can be partly regenerated by hot water and NaOH solution. The percentage of regeneration for the spent AC was 70.4% with 90°C water temperature and up to 95% when 5% NaOH was added into the regeneration solution. These findings are very important for developing efficient adsorbents for the removal of these newly emerging PFASs from wastewater and understanding their interfacial behaviour.

2013 ◽  
Vol 726-731 ◽  
pp. 1687-1690
Author(s):  
Jing Zhang ◽  
Jian Song Liu ◽  
Chun Liu ◽  
Jing Liang Yang ◽  
Lei Zhang

The structure and surface chemical properties of activated carbon after nitric acid modification and their influences on adsorption and catalytic ozonation of acid red 3R were investigated. The results showed that both specific surface area and micropore volume of activated carbon decreased, but mesopore volume increased after nitric acid modification. The adsorption capacity and catalytic ozonation performance of modified activated carbon were influenced due to the increased surface acidic functional groups. The adsorption capacity of modified activated carbon was enhanced under acidic condition due to dispersion interaction between increased surface acidic functional groups and acid red 3R. The increase in surface acidic functional groups of activated carbon was also considered to be responsible for improvement of the catalytic ozonation of acid red 3R under alkaline condition, because of their participation in the ozone decomposition and OH generation.


2012 ◽  
Vol 12 (3) ◽  
pp. 398-405 ◽  
Author(s):  
Tongmian Liu ◽  
Fuyi Cui ◽  
Dongmei Liu ◽  
Zhiwei Zhao ◽  
Zhiquan Liu ◽  
...  

Coal-based activated carbon (AC) was treated chemically with nitric acid, sodium hydroxide and ammonia, and its ability to adsorb bromate was investigated. Several techniques were used to characterize the physicochemical properties of these materials, including surface area, pHpzc, and Boehm titration. Results indicated that surface physical and chemical properties can influence the adsorption uptake of bromate on ACs simultaneously. Surface basicity and pHpzc were both found to influence the electrostatic interactions between the bromate ions and the surface of the carbon. A correlation was found between basic groups and the adsorption capacity for bromate. The adsorption capacity of the carbon was found to be linearly proportional to the amount of basic groups on the surface. The bromate adsorption data collected from all the samples were found to fit the Toth isotherm model, indicating that the bromate adsorption process could occur on heterogeneous surfaces.


2016 ◽  
Vol 57 (60) ◽  
pp. 29137-29142 ◽  
Author(s):  
Su-Huan Kow ◽  
Muhammad Ridwan Fahmi ◽  
Che Zulzikrami Azner Abidin ◽  
Soon-An Ong ◽  
Naimah Ibrahim

2013 ◽  
Vol 726-731 ◽  
pp. 1883-1889
Author(s):  
Brim Stevy Ondon ◽  
Bing Sun ◽  
Zhi Yu Yan ◽  
Xiao Mei Zhu ◽  
Hui Liu

Microwave energy was used to prepare modified activated carbons (GAC, GAC/MW, GAC/Ni, and GAC/Cu). The modified activated carbons were used for phenol adsorption in aqueous solution. The adsorption conditions were optimized. Adsorption capacities of the different modified activated carbons were evaluated. The effect of microwave pretreatment of activated carbons was investigated. A comparative study on the activated carbons adsorption capacities was also investigated. Under optimal conditions the results showed that there was no obvious effect on activated carbons adsorption when rising temperature and pH during the adsorption process. Stirring has a very high effect on the activated carbons adsorption capacity. The adsorption capacity of the modified activated carbons reaches 95%. MW/GAC, GAC/Ni and GAC/Cu adsorptive capacity was higher compared to the Granulated Activated Carbon (GAC) used as received. GAC treated with microwave energy has highest adsorption capacity. The adsorption capacity of GAC loaded with ion Ni2+ is higher than the activated carbon loaded with Cu2+. The untreated GAC has the lowest adsorption capacity. These results can be explained by the effect of microwave irradiation on GAC.The activated carbon loaded with Ni2+ adsorbs more microwave energy than the GAC loaded with Cu2+.


Materials ◽  
2019 ◽  
Vol 12 (8) ◽  
pp. 1253 ◽  
Author(s):  
Julien Kiener ◽  
Lionel Limousy ◽  
Mejdi Jeguirim ◽  
Jean-Marc Le Meins ◽  
Samar Hajjar-Garreau ◽  
...  

Transition metal hexacyanoferrate/microporous activated carbon composites were obtained using a simple successive impregnation approach. The effect of metal type (nickel, indium, or copper), and the carbon oxidation on the composite characteristics (porosity, metal structure, and particle size), as well as on the removal efficiency of cesium from aqueous solution was investigated. Successful formation of the desired metal hexacyanoferrate phase was achieved and the size of the metallic nanoparticles and their dispersion in the carbon network was found to depend on the metal type, with the indium and nickel-based materials exhibiting the smallest particle size distribution (< 10 nm). Adsorption tests performed under batch conditions demonstrate that the copper hexacyanoferrate/activated carbon composite present the highest cesium removal capacity from aqueous solution (74.7 mg·g−1) among the three studied metal-based nanocomposites. The carbon oxidation treatment leads to the increase in the number of functional groups to the detriment of the porosity but allows for an improvement in the Cs adsorption capacity. This indicates that the Cs adsorption process is governed by the carbon surface chemistry and not its porosity. Moreover, combining oxidized carbon support with copper hexacyanoferrate induces the highest cesium adsorption capacity (101.5 mg·g−1). This could be related to synergistic effects through two absorption mechanisms, i.e., a cation exchange mechanism of Cs with the metallic hexacyanoferrate phase and Cs adsorption via carbon oxygen surface groups, as demonstrated using X-ray photoelectron spectroscopy (XPS) analyses.


2018 ◽  
Vol 55 (4C) ◽  
pp. 245
Author(s):  
Pham Thi Hai Thinh

Ion exchange capacity of oxidized activated carbon (OAC) by HNO3 and surface treatment by NaOH solution was investigated. The HNO3oxidizedfunctional groups on the activated carbon surface, such as ketone, carboxylic acid and its derivatives, to maximum oxidation state. The OAC surface played the role as cation exchanger for adsorption of inorganic compounds, especially metallic cations. The adsorption capacity of OAC was investigated in batch mode with three representative ions with different valence from +1 to +3 (NH4+, Ca2+, Cr3+). The adsorption process was demonstrated by Langmuir and Freundlich isothermal model, and the maximum adsorption capacity according to Langmuir isothrermal equation was 20.4 mg/g for NH4+, 43.5 mg/g for Ca2+ and 38.5 mg/g for Cr3+. The results showed the OAC modified by HNO3 and surface treatment by NaOH solution improved adsorption capacity of AC for cations in solution to a higher level. 


2019 ◽  
Vol 358 ◽  
pp. 160-169 ◽  
Author(s):  
Prashanth Suresh Kumar ◽  
Leon Korving ◽  
Karel J. Keesman ◽  
Mark C.M. van Loosdrecht ◽  
Geert-Jan Witkamp

Sign in / Sign up

Export Citation Format

Share Document