Use of Biomass for Removal of Arsenic Compounds

2012 ◽  
Vol 51 (4) ◽  
pp. 324-335 ◽  
Author(s):  
L. Ansone ◽  
M. Klavins ◽  
A. Robalds ◽  
A. Viksna
Keyword(s):  
Sorption Capacity ◽  
Water Contamination ◽  
Environmentally Friendly ◽  
Kinetic Studies ◽  
Cost Effective ◽  
Arsenic Compounds ◽  
Natural Materials ◽  
Rate Law ◽  
Pseudo Second Order ◽  
Removal Of Arsenic

Water contamination with arsenic compounds is a serious problem. One of the solutions is to develop new sorbents based on natural materials that would be cost-effective and environmentally friendly. New sorbents based on biomaterial impregnation with iron oxyhydroxides have been developed. Raw peat material, iron modified-peat, sand, iron modifiedbiomass (shingles, straw) were used for removal of arsenic compounds. The highest sorption capacity was observed for iron modified-peat. Kinetic studies indicated that most of arsenates were removed within 2 hours, and arsenate sorption on iron modified-peat was characterized by the pseudo-second order rate law.

Adsorption and Desorption Potential of Cadmium Using Green Algae: Equilibrium and Kinetic Studies

2015 ◽  
Vol 1130 ◽  
pp. 693-696 ◽  
Author(s):  
Z.S. Birungi ◽  
E.M.N. Chirwa
Keyword(s):  
Sorption Capacity ◽  
Regression Coefficient ◽  
Kinetic Studies ◽  
Adsorption And Desorption ◽  
First Order ◽  
Rate Of Reaction ◽  
Freshwater Bodies ◽  
Pseudo Second Order ◽  
Better Than ◽  
Stichococcus Bacillaris

Microalgae has a diversity of species found in freshwater bodies but only a few have been explored for their biosorption potential as compared to macro algae (sea weed). Equilibrium and kinetic experiments were used to estimate sorption capacity and rate of reaction respectively. Chloroidium saccharophilum had the highest sorption capacity (qmax) of 200 mg/g and lower affinity (b) of 0.0095 L/g for removal of Cd. However, Stichococcus bacillaris was the best adsorbent for Cd as it had both a higher qmaxand higher b of 125 and 0.049 L/g. The Langmuir and Pseudo-second order models performed better than the Freundlich and First-order models with a regression coefficient (R2) > 0.9. Adsorption and desorption efficiency was achieved highest for Stichococcus bacillaris at 95.8% and 73.49% respectively.

scholarly journals Sorption of Arsenic(III) from wastewater using Prosopis spicigera L. wood (PsLw) carbon-polyaniline composite

2021 ◽  
Vol 13 (4) ◽  
pp. 1283-1293
Author(s):  
Ramasubbu Dhana Ramalakshmi ◽  
Mahalingam Murugan ◽  
Vincent Jeyabal
Keyword(s):  
Public Health Problem ◽  
Kinetic Studies ◽  
Maximum Adsorption Capacity ◽  
Direct Oxidation ◽  
Toxic Heavy Metal ◽  
Pseudo Second Order ◽  
Equilibrium Process ◽  
Removal Of Arsenic ◽  
Efficient Adsorbent ◽  
Good Agreement

Water contamination by toxic heavy metal ions causes a serious public health problem for humans. The present work reports the development of a new adsorbent of PsLw carbon-polyaniline composite by direct oxidation polymerisation of aniline with PsLw carbon for the removal of arsenic (As).  The structure and morphologies of the adsorbent were characterised by Fourier transform infrared spectroscopy (FTIR) and Scanning electron microscopy (SEM). The ability of the adsorbent for the removal of As(III) was estimated by batch and kinetic studies. The optimum adsorption behaviour of the adsorbent was measured at pH=6.0. The equilibrium process was found to be in good agreement with Langmuir adsorption isotherm and the maximum adsorption capacity was 98.8 mg/g for an initial concentration of 60 mg/L at 30 °C. The kinetic study followed pseudo-second-order kinetics. Thermodynamic parameters predict the spontaneous, feasible and exothermic nature of adsorption. Column operation was carried out to remove As(III) bulk and column data obeys the Thomas model. The results indicated that PsLw carbon-polyaniline composite can be employed as an efficient adsorbent than polyaniline for removal of As(III) from wastewater.

scholarly journals Removal of arsenic compounds with peat, peat-based and synthetic sorbents / Usuwania związków arsenu za pomocą torfu, sorbentów na bazie torfu i sorbentów syntetycznych

2012 ◽  
Vol 19 (4) ◽  
pp. 513-531
Author(s):  
Linda Ansone ◽  
Linda Eglite ◽  
Maris Klavins
Keyword(s):  
Thermodynamic Parameters ◽  
Sorption Capacity ◽  
Arsenic Speciation ◽  
Sorption Process ◽  
Iron Compounds ◽  
Arsenic Compounds ◽  
Global Problem ◽  
New Approaches ◽  
Cation Exchangers ◽  
Removal Of Arsenic

Abstract Arsenic contamination of waters is a global problem; therefore, new approaches for its removal are needed. Peat, peat modified with iron compounds, iron humates and polymeric cation exchangers modified with iron were prepared and tested for sorption of arsenic compounds in comparison with weakly basic anionites. The highest sorption capacity was observed when peat sorbents modified with iron compounds were used. Sorption of different arsenic speciation forms onto iron-modified peat sorbents was investigated as a function of pH and temperature. It was established that sorption capacity increases with a rise in temperature, and the calculation of sorption process thermodynamic parameters indicates the spontaneity of sorption process and its endothermic nature.

scholarly journals Use of peat-based sorbents for removal of arsenic compounds

2013 ◽  
Vol 11 (6) ◽  
pp. 988-1000 ◽  
Author(s):  
Linda Ansone ◽  
Maris Klavins ◽  
Linda Eglite
Keyword(s):  
Arsenic Speciation ◽  
Sorption Process ◽  
Sorption Kinetics ◽  
Iron Compounds ◽  
Arsenic Compounds ◽  
Solution Ph ◽  
Pseudo Second Order ◽  
Sorbent Materials ◽  
Removal Of Arsenic ◽  
First Time

AbstractIt is important to apply sorbent materials for purification of water from arsenic contamination due to serious arsenic pollution worldwide. We have developed new sorbents based on natural materials that provide a cheap and environmentally friendly alternative. For the first time, peat modified with iron compounds and iron humates were tested for sorption of arsenic compounds. The highest sorption capacity was found in peat modified with iron compounds. We have found that sorption of different arsenic speciation forms was strongly dependent on solution pH, reaction time and temperature. Calculations of the sorption process using thermodynamic parameters indicate the spontaneity of sorption process and its endothermic nature. Sorption kinetics showed that most arsenates are removed within 2 hours, and the kinetics of arsenate sorption on modified peat can be described by the pseudo-second order mechanism.

Kinetic Behaviour of Amylase According to pH: A New Perspective for Starch Hydrolysis Process

2020 ◽  
Vol 16 (2) ◽  
pp. 135-144
Author(s):  
Ravneet K. Grewal ◽  
Baldeep Kaur ◽  
Gagandeep Kaur
Keyword(s):  
Metal Ions ◽  
Competitive Inhibition ◽  
Deae Cellulose ◽  
Kinetic Studies ◽  
Cost Effective ◽  
Starch Hydrolysis ◽  
Divalent Metal Ions ◽  
Activity Data ◽  
Time Saving ◽  
Alkaline Conditions

Background: Amylases are the most widely used biocatalysts in starch saccharification and detergent industries. However, commercially available amylases have few limitations viz. limited activity at low or high pH and Ca2+ dependency. Objective: The quest for exploiting amylase for diverse applications to improve the industrial processes in terms of efficiency and feasibility led us to investigate the kinetics of amylase in the presence of metal ions as a function of pH. Methods: The crude extract from soil fungal isolate cultures is subjected to salt precipitation, dialysis and DEAE cellulose chromatography followed by amylase extraction and is incubated with divalent metal ions (i.e., Ca2+, Fe2+, Cu2+, and Hg2+); Michaelis-Menton constant (Km), and maximum reaction velocity (Vmax) are calculated by plotting the activity data obtained in the absence and presence of ions, as a function of substrate concentration in Lineweaver-Burk Plot. Results: Kinetic studies reveal that amylase is inhibited un-competitively at 5mM Cu2+ at pH 4.5 and 7.5, but non-competitively at pH 9.5. Non-competitive inhibition of amylase catalyzed starch hydrolysis is observed with 5mM Hg2+ at pH 9.5, which changes to mixed inhibition at pH 4.5 and 7.5. At pH 4.5, Ca2+ induces K- and V-type activation of amylase catalyzed starch hydrolysis; however, the enzyme has V-type activation at 7mM Ca2+ under alkaline conditions. Also, K- and V-type of activation of amylase is observed in the presence of 7mM Fe2+ at pH 4.5 and 9.5. Conclusion: These findings suggest that divalent ions modulation of amylase is pH dependent. Furthermore, a time-saving and cost-effective solution is proposed to overcome the challenges of the existing methodology of starch hydrolysis in starch and detergent industries.

scholarly journals Kinetics and isotherm modeling of Pb(II) and Cd(II) sequestration from polluted water onto tropical ultisol obtained from Enugu Nigeria

2021 ◽  
Vol 11 (4) ◽  
Author(s):  
Theresa C. Umeh ◽  
John K. Nduka ◽  
Kovo G. Akpomie
Keyword(s):  
Metal Ions ◽  
Low Cost ◽  
Water Environment ◽  
Standard Technique ◽  
Soil Surface ◽  
Cost Effective ◽  
Polluted Water ◽  
Batch Adsorption ◽  
Lead And Cadmium ◽  
Pseudo Second Order

AbstractDeterioration in soil–water environment severely contributed by heavy metal bioavailability and mobility on soil surface and sub-surface due to irrational increase in wastewater discharge and agrochemical activities. Therefore, the feasibility of adsorption characteristics of the soil is paramount in curbing the problem of micropollutant contamination in the farming vicinity. Soil from a farming site in a populated area in Enugu, Nigeria was collected and tested to measure the lead and cadmium contents using atomic absorption spectrophotometer (AAS). The adsorption potency of the ultisol soil was estimated for identifiable physicochemical properties by standard technique. The mean activity concentration of Pb2+ and Cd2+ was 15.68 mg/kg and 3.01 mg/kg. The pH, temperature, metal concentration and contact time adsorptive effect on the Pb2+ and Cd2+ uptake was evaluated by batch adsorption technique. The Langmuir, Freundlich and Temkin models were fitted into equilibrium adsorption data and the calculated results depict a better and satisfactory correlation for Langmuir with higher linear regression coefficients (Pb2+, 0.935 and Cd2+, 0.971). On the basis of sorption capacity mechanism of the soil, pseudo-second-order model best described the kinetics of both metal ions retention process. The results of the present study indicated that the soil being a low cost-effective adsorbent can be utilized to minimize the environmental risk impact of these metal ions.

scholarly journals Development of Biochars Derived from Water Bamboo (Zizania latifolia) Shoot Husks Using Pyrolysis and Ultrasound-Assisted Pyrolysis for the Treatment of Reactive Black 5 (RB5) in Wastewater

Water ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 1615
Author(s):  
Thanh Tam Nguyen ◽  
Hung-Hsiang Chen ◽  
Thi Hien To ◽  
Yu-Chen Chang ◽  
Cheng-Kuo Tsai ◽  
...  
Keyword(s):  
Cost Effective ◽  
Reactive Black 5 ◽  
Order Kinetic ◽  
Sem Images ◽  
Zizania Latifolia ◽  
Surface Areas ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ultrasound Assisted ◽  
Green Technique

Adsorbent made by carbonization of biomass under oxygen-limited conditions has become a promising material for wastewater treatment owing to its cost-effective, simple, and eco-friendly processing method. Ultrasound is considered a green technique to modify carbon materials because it uses water as the solvent. In this study, a comparison of Reactive Black 5 (RB5) adsorption capacity between biochar (BC) generated by pyrolysis of water bamboo (Zizania latifolia) husks at 600 °C and ultrasound-assisted biochar (UBC) produced by pyrolysis at 600 °C assisted by ultrasonic irradiation was performed. UBC showed a greater reaction rate and reached about 80% removal efficiency after 4 h, while it took 24 h for BC to reach that level. Scanning electron microscope (SEM) images indicated that the UBC morphology surface was more porous, with the structure of the combination of denser mesopores enhancing physiochemical properties of UBC. By Brunauer, Emmett, and Teller (BET), the specific surface areas of adsorbent materials were analyzed, and the surface areas of BC and UBC were 56.296 m2/g and 141.213 m2/g, respectively. Moreover, the pore volume of UBC was 0.039 cm3/g, which was higher than that of BC at 0.013 cm3/g. The adsorption isotherms and kinetics revealed the better fits of reactions to Langmuir isotherm and pseudo-second-order kinetic model, indicating the inclination towards monolayer adsorption and chemisorption of RB5 on water bamboo husk-based UBC.

scholarly journals The sorption of inorganic arsenic on modified sepiolite: Effect of hydrated iron(III)-oxide

2014 ◽  
Vol 79 (7) ◽  
pp. 815-828 ◽  
Author(s):  
Nikola Ilic ◽  
Slavica Lazarevic ◽  
Vladana Rajakovic-Ognjanovic ◽  
Ljubinka Rajakovic ◽  
Djordje Janackovic ◽  
...  
Keyword(s):  
Sorption Capacity ◽  
Arsenic Removal ◽  
Ph Value ◽  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Deionized Water ◽  
Order Kinetic ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The sorption of inorganic arsenic species, As(III) and As(V), from water by sepiolite modified with hydrated iron(III) oxide was investigated at 25 ?C through batch studies. The influence of the initial pH value, the initial As concentrations, the contact time and types of water on the sorption capacity was investigated. Two types of water were used, deionized and groundwater. The maximal sorption capacity for As(III) from deionized water was observed at initial and final pH value 7.0, while the bonding of As(V) was observed to be almost pH independent for pH value in the range from 2.0 to 7.0, and the significant decrease in the sorption capacity was observed at pH values above 7.0. The sorption capacity at initial pH 7.0 was about 10 mg g?1 for As(III) and 4.2 mg g?1 for As(V) in deionized water. The capacity in groundwater was decreased by 40 % for As(III) and by 20 % for As(V). The Langmuir model and pseudo-second order kinetic model revealed good agreement with the experimental results. The results show that Fe(III)-modified sepiolite exhibits significant affinity for arsenic removal and it has a potential for the application in water purification processes.

Removal of Mg from spring water using natural clinoptilolite

Clay Minerals ◽  
2012 ◽  
Vol 47 (1) ◽  
pp. 81-92 ◽  
Author(s):  
S. Tomić ◽  
N. Rajić ◽  
J. Hrenović ◽  
D. Povrenović
Keyword(s):  
Ion Exchange ◽  
Kinetic Studies ◽  
Spring Water ◽  
Zeolite A ◽  
Zeolitic Tuff ◽  
Rate Limiting Step ◽  
Intra Particle Diffusion ◽  
Pseudo Second Order ◽  
Natural Clinoptilolite ◽  
Rate Limiting

AbstractNatural zeolitic tuff from Brus (Serbia) consisting mostly of clinoptilolite (about 90%) has been investigated for the reduction of the Mg concentration in spring water. The sorption capacity of the zeolite is relatively low (about 2.5 mg Mg g-1for the initial concentration of 100 mg Mg dm-3). The zeolitic tuff removes Mg from water solutions by ion exchange, which has been demonstrated by energy dispersive X-ray analysis (EDS). The extent of ion exchange was influenced by the pH and the initial Mg concentration. Kinetic studies revealed that Lagergen's pseudo-second order model was followed. Intra-particle diffusion of Mg2+influenced the ion exchange, but it is not the rate-limiting step. Rather than having to dispose of the Mg-loaded (waste) zeolite, a possible application was tested. Addition to a wastewater with a low concentration of Mg showed that it could successfully make up for the lack of Mg micronutrient and, accordingly, enabled the growth of phosphate-accumulating bacteriaA. Junii, increasing the amount of phosphate removed from the wastewater.

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