Adsorption of Selected Pharmaceuticals and an Endocrine Disrupting Compound by Granular Activated Carbon. 1. Adsorption Capacity and Kinetics

2009 ◽  
Vol 43 (5) ◽  
pp. 1467-1473 ◽  
Author(s):  
Zirui Yu ◽  
Sigrid Peldszus ◽  
Peter M. Huck
Keyword(s):  
Activated Carbon ◽  
Adsorption Capacity ◽  
Granular Activated Carbon ◽  
Endocrine Disrupting Compound ◽  
Endocrine Disrupting

scholarly journals Electroadsorption of Bromide from Natural Water in Granular Activated Carbon

Water ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 598
Author(s):  
David Ribes ◽  
Emilia Morallón ◽  
Diego Cazorla-Amorós ◽  
Francisco Osorio ◽  
María J. García-Ruiz
Keyword(s):  
Activated Carbon ◽  
Electric Field ◽  
Adsorption Capacity ◽  
Natural Water ◽  
Granular Activated Carbon ◽  
Open Circuit ◽  
Filter Press ◽  
Anodic Treatment ◽  
Positive Polarization ◽  
Two Stages

The adsorption and electroadsorption of bromide from natural water has been studied in a filter-press electrochemical cell using a commercial granular activated carbon as the adsorbent. During electroadsorption experiments, different voltages were applied (2 V, 3 V and 4 V) under anodic conditions. The presence of the electric field improves the adsorption capacity of the activated carbon. The decrease in bromide concentration observed at high potentials (3 V or 4 V) may be due to the electrochemical transformation of bromide to Br2. The anodic treatment produces a higher decrease in the concentration of bromide in the case of cathodic electroadsorption. Moreover, in this anodic electroadsorption, if the system is again put under open circuit conditions, no desorption of the bromide is produced. In the case of anodic treatment in the following adsorption process after 24 h of treatment at 3 V, a new decrease in the bromide concentration is observed as a consequence of the decrease in bromide concentration after the electrochemical stage. It can be concluded that the electroadsorption process is effective against the elimination of bromide and total bromine in water, with a content of 345 and 470 µg L−1, respectively, reaching elimination values of 46% in a single-stage electroadsorption process in bromide and total bromine. The application of the electric field to the activated carbon with a positive polarization (anodic electroadsorption) increases the adsorption capacity of the activated carbon significantly, achieving a reduction of up to 220 µg L−1 after 1 h of contact with water. The two stage process in which a previous electrochemical oxidation is incorporated before the electroadsorption stage significantly increased the efficiency from 46% in a single electroadsorption step at 3 V, to 59% in two stages.

Application of Carbonaceous Materials to Phenol Removal from Aqueous Solution by Adsorption

2012 ◽  
Vol 164 ◽  
pp. 297-301 ◽  
Author(s):  
Wei Fang Dong ◽  
Li Hua Zang ◽  
Qing Chao Gong ◽  
Cun Cun Chen ◽  
Cai Hong Zheng ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Adsorption Capacity ◽  
Petroleum Coke ◽  
Granular Activated Carbon ◽  
Powdered Activated Carbon ◽  
Maximum Adsorption Capacity ◽  
Phenol Removal ◽  
Carbonaceous Materials ◽  
Solution Ph ◽  
Equilibrium Studies

Low cost carbonaceous materials were evaluated for their ability to remove phenol from wastewater. The effects of adsorbents dosage, contact time and maximum adsorption capacity were investigated for granular activated carbon, powdered activated carbon, petroleum coke and multi-walled carbon nanotube (MWNT). Equilibrium studies were conducted in 50mg/L initial phenol concentration, solution pH of 5 and at temperature of 23°C. The results showed the adsorption process was fast and it reached equilibrium in 3 h. Petroleum coke and MWNT had poor adsorption which could reach the removal efficiency of phenol with 43.18% and 36.64% respectively. The granular activated carbon possessed good adsorption ability to phenol with 96.40% at the optimum dosage 5g and optimum time 90min.The powdered activated carbon was an effective adsorbent with a maximum adsorption capacity of 42.32 mg/g.

Experimental validation of a test to estimate the remaining adsorption capacity of granular activated carbon for taste and odour compounds

2019 ◽  
Vol 5 (3) ◽  
pp. 609-617 ◽  
Author(s):  
Yifeng Huang ◽  
Zhijie Nie ◽  
Jie Yuan ◽  
Audrey Murray ◽  
Yi Li ◽  
...  
Keyword(s):  
Drinking Water ◽  
Activated Carbon ◽  
Water Treatment ◽  
Adsorption Capacity ◽  
Experimental Validation ◽  
Drinking Water Treatment ◽  
Granular Activated Carbon ◽  
Adsorptive Capacity

A test was developed to measure the present-day adsorptive capacity of granular activated to help drinking water treatment professionals to determine when the GAC needs replacement.

Effects of molecular oxygen on GAC adsorption of energetics

1997 ◽  
Vol 35 (7) ◽  
pp. 197-204 ◽  
Author(s):  
Sarah L. VanderLoop ◽  
Makram T. Suidan ◽  
Sandra R. Berchtold ◽  
Moustafa A. Moteleb ◽  
Stephen W. Maloney
Keyword(s):  
Catalytic Activity ◽  
Activated Carbon ◽  
Adsorption Capacity ◽  
Molecular Oxygen ◽  
Waste Treatment ◽  
Granular Activated Carbon ◽  
Adsorption Properties ◽  
Chemical Degradation ◽  
Degradation Reactions ◽  
Gac Adsorption

Munitions wastewaters are commonly treated by granular activated carbon (GAC) adsorption followed by incineration of the spent carbon. The design of effective GAC unit processes hinges on the knowledge of GAC adsorption capacity for the compounds of interest as well as the types of chemical interactions to expect. GAC can often catalyze polymerization or chemical degradation of the adsorbate in the presence of molecular oxygen. Some adsorbates, though less common, may be subject to catalytic activity even when no molecular oxygen is present. The products of these interactions may enhance or interfere with effective waste treatment. This study individually evaluated the adsorption properties of a variety of energetics compounds. A number of surface catalyzed polymerization and degradation reactions were noted.

scholarly journals Adsorption by Granular Activated Carbon and Nano Zerovalent Iron from Wastewater: A Study on Removal of Selenomethionine and Selenocysteine

Water ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 23
Author(s):  
Stanley Onyinye Okonji ◽  
Linlong Yu ◽  
John Albino Dominic ◽  
David Pernitsky ◽  
Gopal Achari
Keyword(s):  
Experimental Data ◽  
Activated Carbon ◽  
Adsorption Capacity ◽  
Inductively Coupled Plasma ◽  
Granular Activated Carbon ◽  
Inhibitory Effect ◽  
Zerovalent Iron ◽  
Driving Mechanism ◽  
Organic Selenium ◽  
Nano Zerovalent Iron

Selenomethionine (SeMet) and selenocysteine (SeCys) are the most common forms of organic selenium, which is often found in the effluent of industrial wastewater. These organic selenium compounds are toxic, bioavailable and most likely to bioaccumulate in aquatic organisms. This study investigated the use of two adsorbent candidates (granular activated carbon (GAC) and nano zerovalent iron (nZVI)) as treatment technologies for SeMet and SeCys removal. Batch experiments were performed and inductively coupled plasma optical emission spectrometer (ICP-OES) was used for sample analysis. Experimental data showed GAC demonstrated a higher affinity towards the removal of SeMet and SeCys compared to nZVI. The removal efficiency of SeCys and SeMet by GAC was 96.1% and 86.7%, respectively. NZVI adsorption capacity for SeCys was 39.4% and SeMet < 1.1%. Irrespective of the adsorbent, SeMet is more refractory to be adsorbed compared to SeCys. Kinetics data of GAC and nZVI agreed well with the pseudo-second-order model (R2 > 0.990). The experimental data of SeCys was characterized by Langmuir model, indicating monolayer adsorption. The adsorption capacity of nZVI for SeCys increased significantly by about 35%, with a decrease in pH from 9.0 to 4.0, indicating that SeCy removal by nZVI is pH dependent. While electrostatic attraction is considered the driving mechanism for nZVI adsorption, GAC uptake capacity is controlled by weak van der Waal forces. The adsorption of binary adsorbates (SeMet and SeCys) exhibited an inhibitory effect due to the competitive interaction between contaminant molecules.

Sign in / Sign up

Export Citation Format

Share Document