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Effect of Pore Size Distribution on Competitive Adsorption of Trace Organic Micropollutants on Activated Carbon in Natural Water

Effect of Pore Size Distribution on Competitive Adsorption of Trace Organic Micropollutants on Activated Carbon in Natural Water PDF Author: Costas Pelekani
Publisher:
ISBN:
Category :
Languages : en
Pages : 208

Book Description


Effect of Pore Size Distribution on Competitive Adsorption of Trace Organic Micropollutants on Activated Carbon in Natural Water

Effect of Pore Size Distribution on Competitive Adsorption of Trace Organic Micropollutants on Activated Carbon in Natural Water PDF Author: Costas Pelekani
Publisher:
ISBN:
Category :
Languages : en
Pages : 208

Book Description


Mechanisms of Competitive Adsorption Between Trace Organic Contaminants and Natural Organic Matter on Activated Carbon

Mechanisms of Competitive Adsorption Between Trace Organic Contaminants and Natural Organic Matter on Activated Carbon PDF Author: Li Ding
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description
Activated carbon adsorption is widely used in water treatment for removal of various organic micropollutants; nonetheless, the presence of natural organic matter (NOM) in source water can reduce its efficiency for micropollutant removal. NOM has been shown to compete with target contaminant via different mechanisms: direct competition for available adsorption sites which reduces equilibrium capacity for target compounds, blocking of pore entrance which reduces diffusion rate of the target compounds, and covering of surface sites which may actually enhances diffusion rate of the target compounds. The objective of this dissertation study was to further elucidate the individual competitive effects, to investigate how pore sizes of adsorbents and molecular structure of competing compounds affect competition and to gain a comprehensive understanding of the competitive adsorption. Atrazine, a widely used herbicide in the United States, was used as the trace-level target contaminant and NOM from different source waters as well as NOM surrogates were used as the competing compounds. Powdered activated carbons (PACs) with different pore size distribution (PSD) were used. The PSD was found to have great influence on the pore blockage (PB) effect caused by NOM. The equilibrium capacity of the NOM used in this study was best correlated to the amount of pores of diameter 15-50 ©5, which was also inversely related to the magnitude of the pore blockage effect. Activated carbon that has more surface area in this pore size range had a smaller PB effect on atrazine adsorption kinetics at the same NOM loading. This finding indicated that mesopores are important in realizing adsorption capacity for trace compounds by alleviating the adverse PB effect. The site covering effect was confirmed with additional types of PACs and various competing compounds. More important, the correlation equation that describes the enhanced surface diffusion coefficient for atrazine as a function of the loading of the site-covering compounds was found to be independent of either the PAC type or the competing compound type. The key component was to quantify the competing compound as the equivalent background compound (EBC), which reflected the extent of active sites being covered. iii The site competing effect, the site covering effect and the pore blocking effect were evaluated for five NOM surrogates with different sizes. The smaller molecules were generally more effective in reducing the equilibrium capacity of the target compound. However, for molecules of similar molecular weight, elongated molecules tended to have more equilibrium effect than round molecules. From a kinetic perspective, the enhancement in diffusivity was within one order of magnitude for all five surrogates, while the extent of the PB effect was greatly relying on molecular size that large-sized surrogates caused a much stronger PB effect. Therefore, the overall kinetic effect was dependent on molecular size and the PB effect was usually dominant except for very small molecules. Consistent with the enhanced kinetics associated with pre-adsorbed site-covering competing compounds, atrazine preloading was found to also increase the diffusion coefficient of atrazine, and the extent of enhancement caused by atrazine was greater than that caused by competing compounds. Several explanations were proposed for the difference, which include the micropore filling hypothesis and the artifact associated with the EBC method that was used for site-covering loading quantification.

Effects of Activated Carbon Characteristics on Organic Contaminant Removal

Effects of Activated Carbon Characteristics on Organic Contaminant Removal PDF Author: Detlef R. U. Knappe
Publisher: IWA Publishing
ISBN: 1843398419
Category : Science
Languages : en
Pages : 100

Book Description
Many water treatment plants need to remove objectionable trace organic compounds, and activated carbon adsorption is often the best available technology. Utilities face the challenge of having to choose from a large variety of activated carbons, and iodine number or BET surface area values are often utilized in the selection process. Although neither parameter correlates well with adsorption capacities, alternative activated carbon selection criteria based on fundamental adsorbent and adsorbate properties are lacking to date. The first objective of this research was to systematically evaluate the effects of activated carbon pore structure and surface chemistry on the adsorption of two common drinking water contaminants: the relatively polar fuel oxygenate methyl tertiary-butyl ether (MTBE) and the relatively nonpolar solvent trichloroethene (TCE). The second objective was to develop simple descriptors of activated carbon characteristics that facilitate the selection of suitable adsorbents for the removal of organic contaminants from drinking water.Originally published by AwwaRF for its subscribers in 2003 This publication can also be purchased and downloaded via Pay Per View on Water Intelligence Online - click on the Pay Per View icon below

Effects of Activated Carbon Surface Chemistry and Pore Structure on the Adsorption of Trace Organic Contaminants from Aqueous Solution

Effects of Activated Carbon Surface Chemistry and Pore Structure on the Adsorption of Trace Organic Contaminants from Aqueous Solution PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description
The principal objectives of this research were (1) to identify activated pore structure and surface chemistry characteristics that assure the effective removal of trace organic contaminants from aqueous solution, and (2) to develop a procedure to predict the adsorption capacity of activated carbons from fundamental adsorbent and adsorbate properties. To systematically evaluate pore structure and surface chemistry effects on the adsorption of organic micropollutants from aqueous solution, a matrix of activated carbon fibers (ACFs) with three activation levels and four surface chemistry levels was prepared and characterized. In addition, three commercially available granular activated carbons (GACs) were studied to verify whether correlations developed for the ACF matrix are valid for adsorbents that are typically used for water treatment. BET surface area, pore size distribution, elemental composition, point of zero charge and infrared spectroscopy data were obtained to characterize the adsorbents. The results showed that the ACF matrix prepared in this study permits a fairly independent evaluation of surface chemistry and pore structure effects on organic contaminant adsorption from aqueous solution. Methyl tertiary-butyl ether (MTBE), a relatively hydrophilic adsorbate, and trichloroethene (TCE), a relatively hydrophobic adsorbate, served as adsorbate probes. To evaluate the effects of natural organic matter (NOM) on MTBE and TCE adsorption capacities, isotherm experiments were conducted in ultrapure water and Sacramento-San Joaquin Delta water. With respect to surface chemistry, both single-solute isotherms and isotherms in the presence of NOM indicated that hydrophobic adsorbents more effectively removed TCE and MTBE from aqueous solution than hydrophilic adsorbents. Enhanced water adsorption on polar surface sites explained the poorer performance of the hydrophilic adsorbents. Based on the elemental composition of the low-ash carbons evaluated in this study, act.

Activated Carbon Adsorption of Trace Organic Compounds

Activated Carbon Adsorption of Trace Organic Compounds PDF Author: Vernon L. Snoeyink
Publisher:
ISBN:
Category : Carbon, Activated
Languages : en
Pages : 130

Book Description


Adsorption Technology in Water Treatment

Adsorption Technology in Water Treatment PDF Author: Eckhard Worch
Publisher: Walter de Gruyter
ISBN: 3110240238
Category : Science
Languages : en
Pages : 344

Book Description
Adsorption processes have played a central role in water treatment for many years but their importance is on the rise with the continuous discoveries of new micropollutants in the water cycle (pharmaceuticals for example). In addition to the classical application in drinking water treatment, other application fields are attracting increasing interest, such as wastewater treatment, groundwater remediation, treatment of landfill leachate, and so on. Based on the author's long-term experience in adsorption research, the scientific monograph treats the theoretical fundamentals of adsorption technology for water treatment from a practical perspective. It presents all the basics needed for experimental adsorption studies as well as for process modelling and adsorber design. Topics discussed in the monograph include: introduction into basic concepts and practical applications of adsorption processes; adsorbents and their characterisation, single and multi-solute adsorption equilibria, adsorption kinetics, adsorption dynamics in fixed-bed adsorbers and fixed-bed adsorber design, regeneration and reactivation of adsorbents, introduction into geosorption processes in bank filtration and groundwater recharge. According to the increasing importance of micropollutants in the water cycle, particular attention is paid to their competitive adsorption in presence of background organic matter. Clear illustrations, extensive literature references and a useful index make this work indispensible for both scientists and technicians involved in water treatment.

The Role of Pore Size Distribution in Competitive Adsorption on Activated Carbon

The Role of Pore Size Distribution in Competitive Adsorption on Activated Carbon PDF Author: Costas Pelekani
Publisher:
ISBN:
Category :
Languages : en
Pages : 588

Book Description


Effects of Activated Carbon Surface Chemistry and Pore Structure on the Absorption of Methyl Tertiary-Butyl Ether and Trichloroethene from Natural Water

Effects of Activated Carbon Surface Chemistry and Pore Structure on the Absorption of Methyl Tertiary-Butyl Ether and Trichloroethene from Natural Water PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

Book Description
Activated carbon adsorption is the best available treatment technology for thecontrol of many objectionable trace organic compounds. Activated carbons are frequentlycharacterized by the iodine number and BET surface area, but these parameters do notcorrelate well with trace organic compound removal from natural water. Therefore, theobjective of this research was to develop activated carbon selection criteria that assure theeffective removal of trace organic contaminants from natural water and to base theselection criteria on the adsorbent's pore structure and surface chemistry. Tosystematically evaluate pore structure and surface chemistry effects, a matrix of activatedcarbon fibers (ACFs) with three activation levels and four surface chemistry levels wasstudied. To evaluate whether adsorption trends established for ACFs were also valid forgranular activated carbon (GAC), ACF results were compared with those obtained forthree commercially available GACs. Adsorption capacities were determined for naturalorganic matter (NOM), for relatively hydrophilic methyl tertiary-butyl ether (MTBE) andrelatively hydrophobic trichloroethene (TCE) in organic-free water, and for MTBE andTCE in the presence of NOM. NOM isotherms showed that DOC adsorption occurredprimarily in pores with diameters in the 11 to 500 Å range and that electrostaticinteractions between NOM and the carbon surface played a role in NOM adsorption. According to both single-solute isotherms and micropollutant isotherms in the presence of NOM, hydrophobic adsorbents more effectively removed TCE and MTBE thanhydrophilic adsorbents. Effective adsorbents for drinking water treatment shouldtherefore contain little oxygen and nitrogen whose presence increases the polarity of theadsorbent surface. Based on the elemental composition of the low-ash carbons evaluatedin this study, activated carbons should have oxygen and nitrogen contents that sum to nomore than 2 to 3 mmol/g to assure sufficient hydrophobicity. In a.

Effect of Surface Groups on Adsorption of Pollutants

Effect of Surface Groups on Adsorption of Pollutants PDF Author: Robert W. Coughlin
Publisher:
ISBN:
Category : Adsorption
Languages : en
Pages : 44

Book Description


Tailoring of the Activation Process of Carbonaceous Adsorbents for Improving Their Adsorption Effectiveness

Tailoring of the Activation Process of Carbonaceous Adsorbents for Improving Their Adsorption Effectiveness PDF Author: Liang Yan
Publisher:
ISBN:
Category :
Languages : en
Pages : 230

Book Description
Activated carbon adsorption is widely used to remove organic matters (both micropollutants and dissolved natural organic matter (DOM)) in water treatment systems. However, economic use and adsorption effectiveness have been major concerns due to not ideal physicochemical characteristics of most current activated carbons. Meanwhile, due to the competitive adsorption effect from DOM, it has been a great challenge to achieve effective micropollutants removal. Therefore, the main objective of this study was to develop activated carbon with specific selectivity for the removal of DOM and another type for effective removal of micropollutants. This will eventually lead to their application in water treatment facility as a sequence of two adsorber beds in series. Chemical activation of bituminous coal by KOH was applied to develop activated carbons. A total of 24 activated carbons with different porous structure and BET surface area were created under different activation conditions. The effect of the different variables of the activation process on critical carbon parameters was analyzed. In this study, phenolic compounds were selected as model compounds to represent micropollutants. In case of phenolic compounds, the oligomerization phenomenon that occurs in the presence of molecular oxygen, must be controlled by limiting the pore size of activated carbon. Therefore, BC-21 with highest microporosity was selected for phenolic compounds removal. In order to understand the impact of BC-21 on oligomerization of phenolics, single solute, binary solute and ternary solute isotherm adsorption were conducted. Meanwhile, commercial activated carbon F400 was used for comparison. These isotherms were collected under anoxic (absence of molecular oxygen) and oxic (presence of molecular oxygen) conditions. All isotherms demonstrated BC-21 has not only better adsorption capacity but also higher regeneration efficiency. BC-41 with highest mesoporosity was used as carbon precursor for DOM removal. Two novel tailoring methods (outgassing and manganese impregnation) were employed to modify the surface chemical characteristics of BC-41. The developed tailored activated carbons (BC-41-OG -argon outgassed and BC-41-MnN - manganese dioxide impregnated) showed much better DOM adsorption rate and equilibrium capacity than F400 and virgin carbon BC-41. The enhanced DOM removal by BC-41-MnN was attributed to the presence of manganese species on the carbon surface. The higher removal of BC-41-OG was due to the higher surface basicity created during the outgassing treatment. It is very common to have micropollutants such as phenolics in the treatment environment. Therefore, the role of phenolic compounds in determining the adsorption effectiveness of DOM using BC-41-OG and BC-41-MnN was further investigated. The results of the kinetic study indicated phenolic compounds have a significant positive effect on the removal rate of DOM. However, the effect on adsorptive capacity of DOM is highly dependent on the surface chemical characteristics of activated carbon. In addition, DOM with different molecular weight distribution demonstrated different extent of influence from oligomerization. The adsorption performance of BC-41-OG and BC-41-MnN was also examined by conducting small column study. The enhanced selectivity in the removal of DOM rather than phenolics was observed for both novel tailored activated carbon as compared to F400.