Fast and efficient adsorptive removal of organic dyes and active pharmaceutical ingredient by microporous carbon: Effect of molecular size and charge

2019 ◽  
Vol 378 ◽  
pp. 122218 ◽  
Author(s):  
Kanika Gupta ◽  
Om P. Khatri
2020 ◽  
Vol 32 (9) ◽  
pp. 2381-2388
Author(s):  
LAM VAN TAN ◽  
HONG THAM NGUYEN THI ◽  
TO UYEN DAO THI ◽  
VAN THUAN TRAN

The use of inorganic layer compounds as adsorbents for organic dyes in water treatment is of increasing interest. In this study, an attempt is made for the synthesis of Mg/Al LDHs by the hydrothermal method. The synthesis temperature was found to significantly affect to the structure of layered double hydroxides (LDHs), as pointed out by FT-IR analysis. In addition, an adsorption capacity of the synthesized LDHs against Congo red in aqueous solutions was investigated and also compared the adsorption results with other dyes such as methylene blue and methyl orange.


Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1431
Author(s):  
Rui Guo ◽  
Lalita Bharadwaj ◽  
Lee D. Wilson

The adsorptive removal of trihalomethanes (THMs) from spiked water samples was evaluated with a series of modified polysaccharide adsorbents that contain β-cylodextrin or chitosan. The uptake properties of these biodegradable polymer adsorbents were evaluated with a mixture of THMs in aqueous solution. Gas chromatography employing a direct aqueous injection (DAI) method with electrolytic conductivity detection enabled quantification of THMs in water at 295 K and at pH 6.5. The adsorption isotherms for the polymer-THMs was evaluated using the Sips model, where the monolayer adsorption capacities ranged between 0.04 and 1.07 mmol THMs/g for respective component THMs. Unique adsorption characteristics were observed that vary according to the polymer structure, composition, and surface chemical properties. The modified polysaccharide adsorbents display variable molecular recognition and selectivity toward component THMs in the mixed systems according to the molecular size and polarizability of the adsorbates.


Gels ◽  
2021 ◽  
Vol 7 (3) ◽  
pp. 112
Author(s):  
Kayee Chan ◽  
Kohki Morikawa ◽  
Nobuyuki Shibata ◽  
Anatoly Zinchenko

DNA–chitosan (DNA–CS) hydrogel was prepared by in situ complexation between oppositely charged DNA and chitosan polyelectrolytes via electrostatic cross-linking to study its adsorption characteristics. The DNA–chitosan hydrogel matrix contains (i) cationic (NH3+) and anionic (PO4–) sites for electrostatic binding with ionic species, (ii) -OH and -NH2 groups and heteroaromatic DNA nucleobases for chelation of heavy metal ions, and (iii) DNA double-helix for recognition and binding to small organic molecules of various structures and polarities. DNA–CS hydrogels efficiently bind with Hg2+, Pb2+, Cd2+, and Cu2+ metal cations of significant environmental concern. Adsorption capacities of DNA–CS hydrogels for studied metal ions depend on hydrogel composition and pH of solution and reach ca. 50 mg/g at neutral pHs. Hydrogels with higher DNA contents show better adsorption characteristics and notably higher adsorption capacity to Hg2+ ions. Because of the co-existence of cationic and anionic macromolecules in the DNA–CS hydrogel, it demonstrates an affinity to both anionic (Congo Red) and cationic (Methylene Blue) dyes with moderate adsorption capacities of 12.6 mg/g and 29.0 mg/g, respectively. DNA–CS hydrogel can also be used for adsorptive removal of pharmaceuticals on conditions that their molecules are sufficiently hydrophobic and have ionogenic group(s). Facile preparation and multitarget adsorption characteristics of DNA–CS hydrogel coupled with sustainable and environmentally friendly characteristics render this system promising for environmental cleaning applications.


2020 ◽  
Vol 16 (1) ◽  
pp. 14-40 ◽  
Author(s):  
Nusrat Tara ◽  
Sharf Ilahi Siddiqui ◽  
Geetanjali Rathi ◽  
Saif Ali Chaudhry ◽  
Inamuddin ◽  
...  

Background: The huge quantity of wastewater, containing poisonous and hazardous dyes, is released by various industries which pollute water in direct and indirect ways. Most of the dyes are a dangerous class of water contaminants which have affected the environment drastically. Some dyes such as congo red, rhodamine B, methylene blue, methyl violet, and crystal violet are a serious threat to human beings. Remediation Method: Numerous methods are available for the removal of dyes from water. Adsorption, being a superior and eco-friendly technique, has advantage of eliminating organic dyes because of the availability of materials as adsorbents. The inexpensive nanomaterials are a more attractive choice for remediation of various dyes due to their unique properties and offer an adequate pathway to adsorb any organic dye from water to overcome its hazardous effects on human health. Results: In this review, we have discussed the latest literature related to various types of synthesis, characterization and uses as adsorbent for highly adsorptive removal capacity of nanoparticles for organic dyes. Conclusion: Adsorption technology provides an attractive pathway for further research and improvement in more efficient nanoparticles, with higher adsorption capacity, for numerous dyes to eliminate the dyes discharged from various industries and thus reduce the contamination of water. Therefore, nanocomposites may contribute to future prospective water treatment process.


2015 ◽  
Author(s):  
◽  
A.K.M. Nazmul Hussain

[ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] The main objective of this research was to develop an improved understanding of natural organic matter (NOM) and heavy metals removal from two water sources: the City of Columbia McBaine Water Treatment Plant and synthetic water samples prepared in the laboratory. Batch experiments were conducted to evaluate the feasibility of utilizing the adsorption process with magnetite, magnetic ion exchange resin (MIEX), and powdered activated carbon (PAC) as adsorbents to reduce the NOM found in natural groundwater. Control and treated samples were studied to determine the removal degree of dissolved organic matter (DOC) and to verify the impact to the formation potential of disinfection by-products (DBPs). There was no clear correlation found between DOC and disinfection byproducts formation potential (THMFP) over the range of DOC values examined in this study. For MIEX applications, this lack of correlation between DOC removal and DBP could be due to partial dissolution of organic components from MIEX itself. The research provides a framework for using adsorption for the removal of NOM and control of DBP. The presence of common groundwater constituents, such as iron, was found to adversely impact the adsorption capacity of NOM onto MIEX. Possible reasons may include- blocking of the ion-exchange sites on MIEX, and the formation of NOM-Fe complexes that may possess different sorption characteristics from pure NOM. The effects of iron in both Fe2+ and Fe3+ states on the adsorption of NOM onto MIEX were evaluated. The removals of TOCs were found to be higher in oxic conditions whereas the removals of UV254s were found to be higher in anoxic conditions. In oxic conditions, MIEX was capable of removing both NOM and iron effectively when coexisting in raw water. Iron could compete with NOM for exchange sites on MIEX at high dosages (>4 ml/L), which in turn could decrease the NOM removal rate. In anoxic conditions, similar removal patterns were observed as those in oxic conditions, except that MIEX adsorbed less iron with increasing iron content in the water samples. The extent of competitive adsorption was dependent on the initial concentration of trace compounds, the initial concentration of NOM, the molecular size of trace compounds, the molecular size distribution of NOM molecules, and the type and dosage of adsorbents. Experiments were also conducted to study the effects of pH, ionic strength and hematite nanoparticles dosage on the adsorptive removal of Co2+ from aqueous solution. It was observed that adsorption was enhanced in neutral pH conditions, comparing to acidic condition and irrespective of ionic strength. Freundlich models were capable of representing the data more satisfactorily than the Langmuir models. The co-ions removed Co in the order Pb2+> Cu2+ >HA. Hematite nanoparticles derived from ferroxane-AA were deposited on porous alumina tubes to develop tubular ceramic membrane for the removal of Co2+. Ferroane-AA loading on ceramic tube was found to be very low; 0.5 g of ferroxane-AA loaded only 1% and 2.0 g of ferroxane-AA loaded 0.7%. The regeneration process was tested for 4 washing cycles without membrane damage. The results of this study indicate that, with the adsorptive removal of cobalt ions from natural groundwater and the ability to adsorb multiple metal ions simultaneously, hematite nanoparticles may offer a potential and suitable remediation method for the removal of cobalt ions. The ferroxane-AA fabrication process takes place in an aqueous environment, does not involve the use of hazardous substances, and has low energy consumption due to the low firing temperature of the ceramic tube. Furthermore, the generation of liquid wastes on site can be avoided during operation. The membranes can be re-used after washing with a basic solution. The materials can be processed for regeneration in a centralized treatment facility for improved liquid waste management. Its compact and user-friendly design allows it to be deployed at the point of use, while it is also flexible to adapt to a larger scale, suitable for water treatment plants.


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