Introduction For remediation of soils and purification of polluted waters, wastewaters, biosorbents might be considered as prospective groups of materials.

Slides:



Advertisements
Similar presentations
Particle size Ions  molecular clusters  nanocrystals  colloids  bulk minerals Small particles can have a significant % of molecules at their surface.
Advertisements

Complexes Complex – Association of a cation and an anion or neutral molecule All associated species are dissolved None remain electrostatically effective.
LEACHATE MANAGEMENT AND TREATMENT
ADSORPTION OF BASIC DYES ONTO LOW- COST ADSORBENTS: ANALYSIS OF THE EQUILIBRIUM STATE NATIONAL WORKSHOP ON “NEW TRENDS IN BIOTECHNOLOGY: THEORY AND APPLICATIONS.
Removal of Cu(II) ions from aqueous solution effluent using Melamine-Formaldehyde-DTPA resin in a fixed-bed up-flow column By Ahmad Baraka Supervisors.
The Kinetics of Sorption of Lead Ion onto Palm Kernel Fiber Yu-Ting Feng 1#, Ming-Huang Wang 1, Wen-Ta Chiu 2,3 and Yuh-Shan Ho 4 * 1 School of Public.
6.i. Modelling environmental processes: kinetic and equilibrium (quasi-thermodynamic) modelling 6(i)
A modified Lagrangian-volumes method to simulate nonlinearly and kinetically adsorbing solute transport in heterogeneous media J.-R. de Dreuzy, Ph. Davy,
Lecture 3. Adsorption on the interphase of liquid-gas Prepared by PhD Falfushynska Halina.
Sorption of Anions Important because: Several nutrients and agricultural chemicals are negatively charged. –Nitrate, phosphate, sulfate, selenate,… Tropical,
ARSENIC REMOVAL Case History Milos Markovic. Arsenic removal m3/day Plant in Subotica-SERBIA.
Enter your fluid composition on the Basis pane. SpecE8 figures concentrations of aqueous and sorbed species, mineral saturation, and gas fugacity. Go to.
Juris Burlakovs, Maris Klavins, Zane Vincevica-Gaile, and Mara Stapkevica University of Latvia MODIFIED CLAY SORBENTS FOR WASTEWATER TREATMENT AND IMMOBILIZATION.
E NVIRONMENTAL CHEMISTRY E 12. water and soil. W ATER AND SOIL Solve problems relating to the removal of heavy- metal ions, phosphates and nitrates from.
Soil Colloids, the final frontier Measuring CEC; sorption concepts; environmental implications.
Characterization of Al-Humic Complexation and Coagulation Mechanism Removal of natural organic matter (NOM) by coagulation using metal coagulants (aluminium.
Conservative and Reactive Solutes Conservative do not react with soil / groundwater Chloride is a good example Sorbed onto mineral grains as well as organic.
Sorption processes in soil general term referring to the retention of material on solid surfaces - can include adsorption, surface precipitation, and polymerization.
IS SOLUBILITY THE ONLY CONTROL ON SOLUTE CONCENTRATIONS? The answer is NO! Solubility often controls the concentrations of major solutes such as Si, Ca,
Caveats – don’t give K d more power than it deserves Kp and Kd are partitioning and distribution coefficients that vary with soil properties, solution.
CE 510 Hazardous Waste Engineering
CE 510 Hazardous Waste Engineering Department of Civil Engineering Southern Illinois University Carbondale Instructor: Dr. L.R. Chevalier Lecture Series.
Environmental chemistry
Adsorption Equilibrium Adsorption vs. Absorption –Adsorption is accumulation of molecules on a surface (a surface layer of molecules) in contact with an.
Complexes Complex – Association of a cation and an anion or neutral molecule Complex – Association of a cation and an anion or neutral molecule All associated.
8/16/20151 BIOSORPTION OF COBALT AND COPPER FROM HYDROMETALLURGICAL SOLUTIONS MEDIATED BY Pseudomonas spp PRESENTATION BY: NONJABULO PRUDENCE DLAMINI.
ADSORPTION ION EXCHANGE RESINS BIOCHEMISTRY Dr. Nasim A P Biochem.
Talal Almeelbi Surface Complexations of Phosphate Adsorption by Iron Oxide.
Cation Exchange Definition: substitution of ions in solution for those held by a mineral grain. Associated with many different types of materials found.
Environmental Processes Partitioning of pollutants 3.i Sorption involving organic matter (between air/soil and water/soil)
STRUCTURAL EVALUATION OF MATERIALS BASED ON XANTHAN GUM AND LIGNIN Irina Elena Raschip, Maria-Cristina Popescu “Petru Poni” Institute of Macromolecular.
1 The Turtle by Ogden Nash Ogden Nash The turtle lives 'twixt plated decks Which practically conceal its sex. I think it clever of the turtle In such a.
Partitioning of pollutants
A unifying model of cation binding by humic substances Class: Advanced Environmental Chemistry (II) Presented by: Chun-Pao Su (Robert) Date: 2/9/1999.
Inorganic Materials Lab. SKKU Sorption Reaction of Aquatic TcO 4 - or CrO 4 2- on Calcined Mg/Al Layered Double Hydroxide: Reaction Equilibria and Characterization.
Phase Interactions Objective –to understand the chemical principles, significance and application of Phase changes in Environmental Engineering. Phase.
EXTRACTION OF COPPER, ZINC AND IRON FROM HYDROCHLORIC ACID SOLUTIONS BY MEANS OF BIFUNCTIONAL EXTRACTANT KELEX 100 Svetlana Zhivkova and George Kyuchoukov.
Entrapment of fungus Rhizomucor tauricus, removal of Zn (II) from aqueous solution and spectroscopic characterization PROF A V N SWAMY, JNTUA College of.
Phosphorus Retention Capacity of a Pilot Stormwater Treatment Area in the Lake Okeechobee Basin Y. Wang 1, K.R. Reddy 1, V. Nair 1, O. Villapando 2, and.
Environmental Processes Partitioning of pollutants 3.ii Sorption involving inorganic matter (between air/soil and water/soil)
An efficient biosorption of direct dyes from industrial wastewaters using pretreated sugarcane bagasse.
Effectiveness and mechanisms of mercury sorption by biochars from invasive Brazilian pepper at different temperatures Xiaoling Dong 1, Lena Q Ma 1*, Yingjia.
Soils and Environmental Pollution Chapter 18. Of these 5 fates, inorganics are subject to 4 –all but degradation. The notion is that the inorganic contaminant.
Nguyen Thi Kim Phuong Institute of Chemical Technology
Solubility (cont.); Mineral Surfaces & Reactions Lecture 22.
Ion Exchange Isotherms Models Thermodynamic Exchange Constant Only ions adsorbed as outer-sphere complexes or in the diffuse ion swarm are exchangeable.
INTRODUCTION Cd Usually it combined with other elements such: oxygen, chlorine, or sulfur. Cd 2+ activities in soils is about M. levels of Cd in.
4 th International Congress of the European Confederation of Soil Science Societies (ECSSS). 2-6 July 2012, Bari – Italy. Removal of Cr (VI) from industrial.
Development of new materials to concentrate nutrients from digestate Ph.D. Student: Antonis Karachalios Principal Investigators: Dr. Mahmoud Wazne Dr.
Introduction : Phosphorus (P) is one of the critical nutrient elements after nitrogen for increasing crop growth and yield. The Phosphatic fertilizers.
7th International YWP conference, Taipei Chinese Taiwan
Adsorption Equilibrium and Kinetic Study for the Removal of Nitrate from Drinking Water Supplies By Chitosan Composite Wondalem Misganaw Golie Dr. Sreedevi.
SIMULTANEOUS ADSORPTION OF 11 VOLATILE ORGANIC COMPOUNDS BY AN ACTIVATED CARBON MADE FROM POLYSTYRENE SULFONIC ACID-BASED ORGANIC SALT.
Phosphate removal from aqueous solution with Fly Ash and Natural Zeolite S. Safari1, D.F.E. Galarza1, Dr. E. Katsou1, Dr. S. Malamis2  1Department of.
Enter your fluid composition on the Basis pane
Materials-palygorskite, tetracycline 1.
Prof. Sergiy Lavrynenko National Technical University “Kh. P. I
Solubility (cont.); Mineral Surfaces & Reactions
Fe-Al binary Oxide Nano-Sorbent: Synthesis, Characterization and Phosphate Sorption Behavior Tofik Ahmed, Abi.M.Taddesse, Tesfahun Kebede, Girma Goro.
Application of Iron Oxide Nanoparticles/silica Composites on the Removal of Uranium(VI) for Drinking Water Treatment and the Impact of Water Chemistry.
Shiue-Chang Lee#, Wen-Ta Chiu and Yuh-Shan Ho*
Chi-Hao Hsiao#, Wen-Ta Chiu and Yuh-Shan Ho*
Adsorption of Basic Dye From Water by Tree Fern
Pseudo-Second Order Model for Lead Ions Removal from Water
Fang-Ching Lee#, Wen-Ta Chiu and Yuh-Shan Ho*
Comparison of Linear and Non-linear Methods on Sorption Isotherm
The 49th International October Conference on Mining and Metallurgy
Teng-Chin Tsai#, Wen-Ta Chiu and Yuh-Shan Ho*
Pei-Yu Lin1#, Ming-Huang Wang1, Wen-Ta Chiu2,3 and Yuh-Shan Ho4*
Sing-On Teng#, Wen-Ta Chiu and Yuh-Shan Ho*
Presentation transcript:

Introduction For remediation of soils and purification of polluted waters, wastewaters, biosorbents might be considered as prospective groups of materials. Amongst them peat have a special role due to low cost, biodegradability, high number of functional groups, well developed surface area and combination of hydrophilic/hydrophobic structural elements. Hybrid biosorbent - natural, biomass based modified material, covered with another sorbent material, thus combining properties of both such as sorbent functionalities and surface properties. As the “covering layer” both inorganic substances, mineral phases (iron oxohydroxides, oxyappatite) and organic polymers (using graft polymerization) were used. Environmental pollution with V and VI group metalloids (As, Sb, Te) – significant environmental problem. Polluted drinking water can cause important threats to the human health. Arsenic contamination of waters is a global problem. More than 40 million people are suffering from As contamination worldwide. Antimony and its compounds were considered as pollutants by USEPA as well as the EU. Antimony like arsenic is toxic and trivalent species are reported to be more toxic than pentavalent. Toxicity of tellurium may induce local environmental problems. Sb as well as As is present in the environment as a result of natural and human activities. Predominant forms of As and Sb in natural waters are As (III), As (V) and Sb (III), Sb (V) accordingly, while tellurium mainly exists as Te (IV) or Te (VI). Inorganic forms of As and Sb in natural waters and soils are intimately related to the presence of iron oxo(hydroxides) being metalloids strongly sorbed onto the surfaces of Fe oxides, forming inner- or outer-sphere surface complexes. Therefore Fe containing sorbents based on different natural materials have found widespread application in water treatment. The aim of this study is to investigate and compare Fe-modified biomaterial application possibilities for metalloid and phosphate sorption, thus reducing their concentration and obtain new effective and perspective sorbents. Juris Burlakovs, Maris Klavins, Artis Robalds, Linda Ansone Department of Environmental Science, University of Latvia, Raina blvd. 19, LV – 1586, Riga, Latvia  The present work investigates the sorption of metalloids (As, Sb, and Te) and phosphates – on Fe-modified biomaterials: peat, shingles, moss and straw using batch tests. Sorption was studied as a function of initial metalloid (or phosphate) concentration, pH, and temperature.  FT-IR spectra, SEM images, nitrogen adsorption isotherm measurements, as well as moisture content, organic substances content, and Fe 2 O 3 analyses were used to characterize the obtained sorbents. Results and Discussion Obtained sorption data have been correlated using Langmuir as well as Freundlich isotherm models. Based on correlation coefficients, metalloid sorption as sorbent using Fe-modified biomaterials better fitted to the Langmuir model with exception of Sb (V) as a sorbent using Fe-modified moss that fitted to Freundlich model. Sorption capacity increases with a rise in temperature. Possible reason could be diffusion rate increase of adsorbate molecules as the temperature raise, as well as changes of sorbent pore size. Linear Langmuir equation form was used to determine Langmuir isotherm constant (K) and thermodynamic parameters. Calculated thermodynamic parameters (ΔG°, ΔH˚, ∆S˚) suggest that sorption process has spontaneous nature and it is endothermic. The positive values of standard entropy show increasing randomness at the solid/liquid interface during the sorption of metalloid ions onto modified peat. Decrease in ∆G˚ with increasing temperature implies stronger sorption at higher temperatures. Materials and Methods Hybrid biosorbents for removal of pollutants and remediation Sorbent modification with Fe compounds and product after graftpolymerization allow to enhance sorption capacity. The reason could be formation of metalloid-O-Fe bond for Fe-modified biosorbents. The highest sorption capacity has Fe-modified peat sorbing As (V), Sb (V) as well as Te (VI). Fe-modified moss and Fe-modified shingles could also be used in severely polluted waters, while Fe-modified straw and Fe-modified canes may be used in areas with low metalloid concentration. Sorbent: Fe-modified peat Material modification with Fe compounds significantly enhanced sorption capacity, possibly due to metalloid-O-Fe bond forming. Fe-modified peat - the best sorbent for As (V), Sb (V) and Te (VI). The best sorption conditions are in the pH interval 3-6 for As (V) and Sb (V), while pH 3 – 9 is the most appropriate interval for Te (VI) removal. The sorption capacity increases with increase in temperature for all studied metalloids and calculated thermodynamic parameters suggest that sorption process has spontaneous nature and it is endothermic. Conclusions Different metalloid concentrations ( mg/L ) ETAAS or FAAS 0.5 g Fe-modified sorbent Stirred for 24 h, filtered Analysis and calculations Results Sorbent: Fe-modified peat It could be supposed that As (V) and Sb (V) as well as Te (VI) sorption onto Fe-modified biosorbents mainly occur considering electrostatic interaction between the ionic species of respective element and the charged surface groups of sorbent. pH zpc values of studied sorbents varies from 3.2 to 5.5. pH zpc of Fe-modified peat is 4.7, the surface of the sorbent is positively charged if pH 4.7, surface of the sorbents become negatively charged and interaction between active sorption sites on the sorbent and negatively charged ions decreases. The decrease of sorption capacity in basic solution could be due to the competition for sorption sites between metalloid anions and hydroxide ions. Speciation of metalloids in aqueous media is suggested to be one of the main factors that cause differences in metalloid removal. The best sorption conditions are in the pH interval 3 – 6 for As (V) and Sb (V), when negatively charged H 2 AsO 4 - and HAsO 4 2- and Sb(OH) 6 - are predominant forms in solution. pH has not significant impact Te (VI) removal at the studied conditions. The maximum sorption capacity reached mg P/g at initial P concentration of 500 mg/L. The sorption capacity of modified peat increased with the increase of the initial phosphate concentration for all temperatures studied (Figure 1). The steep rise of the isotherm curve close to its origin indicates high uptake values at low concentrations. 99 % of phosphate ions had been sorbed at initial concentration range mg P/L, which is a range typical for wastewaters. The positive values of standard entropy show increasing randomness at the solid/liquid interface during the sorption of metalloid ions onto modified peat Taking into account the low cost and availability, the use of peat based sorbents may be considered as alternative to conventional wastewater treatment methods Supplementary experiments should be carried out to evaluate the performance of developed sorbents in field scale systems – in constructed wetlands or in bed systems. Characterization of Sorbents SEM of iron modified peat REMOVAL of PHOSPHATES ACKNOWLEDGEMENTS - This work has been supported by the Latvia State Research Program within the project “Sustainable Use of Local Resources – New Products and Technologies” (NatRes).