PREPARATION OF SYNTHETIC ZEOLITES FROM COAL FLY ASH. Shamsul Kamal Sulaiman

Similar documents
Recycling of Municipal Solid Waste Ash through an Innovative Technology to Produce Commercial Zeolite material of High Cation Exchange Capacity

Effective Synthesis of Artificial Zeolite from Coal Fly Ash

SYNTHESIS OF ZEOLITE FROM

Reactivity of Cesium and Fly Ash under Hydrothermal Conditions with NaOH Solution

SYNTHESIS OF FAUJASITE WITH HIGH THERMAL STABILITY FROM FLY ASH

SYNTHESIS AND CHARACTERIZATION OF NA-P ZEOLITE FROM COAL FLY ASH

Science & Technologies SYNTHESIS AND SPECTROSCOPIC STUDY OF ZEOLITE A TYPE AND X TYPE

Synthesis of ZSM-5 zeolite from lignite fly ash and rice husk ash

Aachen, Germany Mine Water Managing the Challenges. Nicholas M. Musyoka¹, Leslie F. Petrik¹, Eric Hums²

Equilibrium ion exchange studies of Zn 2+, Cr 3+ and Mn 2+ on natural bentonite

Synthesis and Testing of Zeolite from Industrial- Waste Coal Fly Ash as Sorbent For Water Adsorption from Ethanol Solution

Characterization of CFB-Coal Fly Ash Zeolitic Materials and Their Potential Use In Wastewater Treatment

Effect of different molarities of Sodium Hydroxide solution on the Strength of Geopolymer concrete

Alkaline Hydrothermal Conversion of Fly Ash Filtrates Into Zeolites 2: Utilization in Wastewater Treatment

A simple thermogravimetric method for the evaluation of the degree of fly ash conversion into zeolite material

Zeolite from fly ash: synthesis and characterization

SNRU Jou r n al of Sc ien ce an d T ech n olo gy 8 ( 3 ) S ep tem ber D ec em be r ( ) SNRU Journal of Science and Technology

INSTRUMENTAL TECHNIQUES

Controlled Release Zeolite Fertilisers: A Value Added Product Produced from Fly Ash

Zeolites: Absorbents, Adsorbents. Prepared for the. Congress April 6 th 9 th, 2003 Montreal, Quebec. LuVerne E.W. Hogg

CHEMICAL REACTION OF FLY ASH

National Technical University of Athens, 9 Iroon Polytechniou Street, Zografou Campus, GR , Athens, Greece

AB3. Nanoscience Advances in CBRN Agents Detection, Information and Energy Security

FORMATION OF CRYSTAL STRUCTURES DURING ACTIVATED CARBON PRODUCTION FROM TURKISH ELBISTAN LIGNITE

SO 2 Removal by Using Jordanian Oil Shale Ash

PETROGRAPHIC MINERALOGICAL ANALYSIS OF AGGREGATES FROM DEVOLL HYDROPOWER PROJECT

Preparation of Iron Oxide Nanoparticles Mixed with Calcinated Laterite for Arsenic Removal

HYDROTHERMAL TECHNOLOGY OF ZEOLITE MATERIALS SYNTHESIS FROM FLY ASH

Multi-stage synthesis of nanopore NaA zeolite membranes for separation of water/ethanol mixtures

SYNTHESIS OF NaA ZEOLITE

Waste Minimization Protocols for the Process of Synthesizing Zeolites from South African Coal Fly Ash

IRUNGU PETER WACHIRA I13/3135/2008

Acid Soil. Soil Acidity and ph

Synthesis of Zeolite A Membrane from Rice Husk Ash

organisms CaCO 3 + H 2 O + CO 2 shallow water

Zeolite synthesis from municipal solid waste ash using fusion and hydrothermal treatment

THE VITREOUS MATRIX PROCESSING OF A WASTE RESULTING FROM ELECTROCHEMICAL DEPOSITION PROCESSES

STUDY ON SORPTION OF SOME TOXIC AND HEAVY IONS IN DILUTE SOLUTIONS BY CLINOPTILOLITE

Direct synthesis of mordenite from kaolin and rice husk ash

Available online at ScienceDirect. Procedia Engineering 121 (2015 )

Malaysian Feldspar: Evaluation and Processing of Selected Deposits

ALPHA OMEGA ZEOLITES FOR THE OILFIELD BRIEF

Dissolution Study of Bottom Ash in Wet Flue Gas Desulphurization

Synthesis of Zeolite X from Waste Sandstone Cake Using Alkali Fusion Method

Hydrothermal Synthesis of Zeolites from Polish Coal Fly Ash

EFFECT OF COMPETING CATIONS (Cu, Zn, Mn, Pb) ADSORBED BY NATURAL ZEOLITE

Removal of Cu 2+ from Aqueous Solution using Fly Ash

Properties of Compounds

Synthesis of Zeolite Composite Membranes for CO2 Separation

Alkali concentrations of pore solution in hydrating OPC

ALKALINE HYDROTHERMAL ZEOLITES SYNTHESIZED FROM FLY ASH SIO 2 AND AL 2 O 3

Microspheres of ly Ash as a Source for Catalytic Supports, Adsorbents and Catalysts

for free revision past papers visit:

APPLICATION OF METAKAOLIN GEOPOLYMER FOR AMMONIUM REMOVAL IN SMALL-SCALE WASTEWATER TREATMENT SYSTEMS

Pozzolanic reactions between natural and artificial aggregate and the concrete matrix

MODULE 4.3 Atmospheric analysis of particulates

Slake Durability of a Deep Red Stratum Sandstone under Different Environments

Current State of Extraction Don t Be Deceived! Sharon F. Webb, Ph.D. Director of Quality Program

TECHNICAL NOTE. ph of Potassium Acetate Deicing Solution

Research on Bipolar Membrane Electrodialysis for Ion Exchange of Molecular Sieves

Sarutt Sripetchr 1* and Surachai Thachepan 2

S. Choudhury* et al. / (IJITR) INTERNATIONAL JOURNAL OF INNOVATIVE TECHNOLOGY AND RESEARCH Volume No. 1, Issue No. 1, December-January 2013,

Quantitative measurement of a mixture of mesophases cubic MCM-48 and hexagonal MCM-41 by 13C CP/MAS NMR

CH 221 Chapter Four Part II Concept Guide

Cation Exchange Capacity, CEC

Supporting Information Appendix

SYNTHESIS OF ZEOLITE FROM FLY ASH AND THE ADSORPTION OF Cu 2+ ION IN WATER SOLUTION

Prajapati et al, International Journal of Advanced Engineering Research and Studies E-ISSN

STUDIES ON THE REMOVAL OF CATIONIC DYES FROM AQUEOUS SOLUTION BY MIXED ADSORBENTS

Modification of surface properties of South African coal fly ash for industrial filler applications

CERAMIC GLAZING as an IGNEOUS PROCESS

Preparation & Characterization of Activated Kaolinite

Elements, Compounds Mixtures Physical and Chemical Changes

LlkJ-/ rpdf Pollution Prevention - Source Reduction with Electrodialytic Processes

Removal of suspended and dissolved organic solids

Geos 306, Mineralogy Final Exam, Dec 12, pts

Geology 560, Prof. Thomas Johnson, Fall 2003 Unit II: Chemical reactions: Guide Questions

Synthesis of zeolites from South African coal fly ash: Investigation of scale-up conditions

Chapter 5. Chemical reactions

EXECUTIVE SUMMARY. especially in last 50 years. Industries, especially power industry, are the large anthropogenic

Adsorption of Free Fatty Acid from Crude Palm Oil on Magnesium Silicate Derived From Rice Husk

DETERMINATION OF BETA EMITTERS IN MATERIALS FROM RESEARCH REACTOR DECOMISSIONING

Molecular Sieves Principles of Synthesis and Identification

Sintering behavior of feldspar rocks

Quantitative Phase Analysis of Ceramic Raw Materials Using a Nonnegative Least Squares Routine

Topsøe Catalysis Forum 2009

Adsorption of Methylene Blue on Mesoporous SBA 15 in Ethanol water Solution with Different Proportions

Synthesis and Characterization Of Bismuth (Iii) Iodotungstate, an Exchanger

Growth and characterization of hydrothermally-grown zeolite crystals

THE MULTI-TECHNIQUE APPROACH

Preparation of Iron Oxide Nanoparticles Mixed with Calcinated Laterite for Arsenic Removal

MOLECULAR SIEVES UOP MOLECULAR SIEVES*

Conducting Polymer /TiO 2 Photocatalytic Nanocomposite for Wastewater Treatment

"PHYSICOCHEMICAL STUDIES OF BASALT-LIKE MATERIALS INTENDED FOR USE AS RADIOACTIVE WASTE IMMOBILIZATION MATRICES "

Lecture 6 Flotation 1. Chapter 8_Flotation of Non-Sulphide Minerals

Sintering of feldspar rocks from czech quarries

SULFUR DIOXIDE REMOVAL

Field Trips. Field Trips

Copyright SOIL STRUCTURE and CLAY MINERALS

Synthesis of Faujasite from Fly Ash and its Applications for Hydrocracking of Petroleum Distillates

Transcription:

Solid State Science and Technology, Vol. 16, No 1 (28) 17-113 ISSN 128-7389 PREPARATION OF SYNTHETIC ZEOLITES FROM COAL FLY ASH Shamsul Kamal Sulaiman Mineral Research Centre, Minerals and Geoscience Department, Jalan Sultan Azlan Shah 314, Ipoh, Perak, Malaysia ABSTRACT Coal Fly ash from Sultan Abdul Aziz Power Station in Kapar, Malaysia was characterized and used for the synthesis of zeolites. Coal Fly ash was pretreated with Wet High Intensity Separation (WHIMS) to remove undesirable iron components prior to the formation of synthetic zeolites. The synthesis method used was a hydrothermal treatment with NaOH activation at low temperature. The hydrothermal reaction produced stable zeolite P which increased in crystallinity as temperature and reaction time increased. Mineral transformation during hydrothermal treatment involved the dissolution of aluminosilicate glass and formation of synthetic zeolite P with a high Cation Exchange Capacity (). INTRODUCTION At present, power stations are facing a serious problem associated with the use of coal for generating electricity. The high temperature burning of coal produces gases such as SOX, NOX and COX together with solid wastes, fly ash being the primary constituent. Due to nature of coal use, which is low in sulphur, and the advanced combustion technology used, the flue gas emmisions can be kept at a level below the maximum limit for air pollution legislation. However, the waste fly ash needs more careful handling due to its solid and lightweight nature. At present, most of the fly ash is dumped in disposal sites. Such sites require a large area and special construction and maintenance, which are quite expensive. Therefore, applications for the utilisation of the waste fly ash are desirable, to reduce the environmental and disposal cost. Hence, the synthesis of zeolites represents a possible use of this material. EXPERIMENTAL METHODS Raw Material The sample of coal fly ash used in this study was obtained from Sultan Abdul Aziz Power Station in Kapar, Selangor. After drying, a representative head sample was prepared by riffling for subsequent chemical, mineralogical and particle size characterisation. Chemical analysis was undertaken by atomic absorption and UV spectrometry; major mineral phases were determined by X-ray diffraction (XRD). All results are listed in Table 1. Magnetic Pre-Treatment of Raw Material Before the hydrothermal process could be used to synthesize zeolite, fly ash samples had to go through a magnetic pre-treatment. Many researchers[1-2] stated that the removal of undesireable iron components prior to the formation of synthetic zeolites improves zeolite crystallization and cation exchange capacity () values of zeolite. The process involved a series of tests using Eriez Wet High Intensity Magnetic Separation (WHIMS). 17

Solid State Science and Technology, Vol. 16, No 1 (28) 17-113 ISSN 128-7389 Table 1: Characterisation of Kapar Coal Fly Ash Raw Fly Ash + 53µm Size Fraction - 53µm Size Fraction %SiO 2 52.11 5.11 53.1 %Al 2 O 3 23.59 21.86 2. %Fe 2 O 3 7.39 8.81 6.98 %TiO 2.88.72.92 %CaO 2.61 1.68 2.4 %MgO.78 1.32 1.8 %Na 2 O.42.41.41 %K 2 O.8.49.78 %P 2 O 5 1.31.6 1.77 %SO 3.49.95.29 %MnO.3.3.2 %Loss on Ignition 5.59 11.28 4.85 Mineral Phases (by XRD) Magnetite Spinel Ferrian Magnetite Spinel Ferrian Magnetite Spinel Ferrian Zeolite Synthesis In each hydrothermal test, a known weight 1g pre-treated raw material was reacted with a solution of sodium hydroxide (NaOH) using various solid-liquid ratios and alkali concentrations. The reaction mixture was heated at various temperatures and reaction times for the formation of zeolite Magnetic Pre-Treatment RESULT AND DISCUSSION Effects of Feed Pulp Density The results of effects of pulp density on Kapar fly ash iron removal tests are shown in Figure 1. As seen from the figure, WHIMS was able to remove maximum of 61.6% of the iron content when the pulp density of the feed was around 2%. The experiments indicated that using Eriez WHIMS with 2% pulp density and 8, Gauss (.8 Tesla) magnetic field intensity, the iron content in Kapar fly ash was reduced from 7.39% to 3.12%. Effects of Magnetic Field Intensity The next series of experiments determined the optimum conditions for magnetic field intensity. In these experiments, the magnetic field intensity was varied from 2, to 11, Gauss (.2 to 1.1 Tesla) and 2% feed pulp density was used throughout. The results of these tests are shown in Figure 2. As seen from the figure, the WHIMS was able to remove more than 6% of the iron content when the magnetic field intensity reached more than 8, Gauss (.8 Tesla). The efficiency of iron removal decreased as the field intensity reached about 9, Gauss (.9 Tesla). The highest iron separation was achieved at a field intensity of 8,7 Gauss (.87 Tesla), whereby 61.69% of the iron component was removed. The remaining iron was probably distributed in the glassy constituent in low concentrations and was difficult to remove by magnetic separation [3]. These results suggest that it is adequate for the fly ash samples to be 18

Solid State Science and Technology, Vol. 16, No 1 (28) 17-113 ISSN 128-7389 pre-treated with WHIMS using conditions of 2% feed pulp density and 8,7 Gauss (.87 Tesla) magnetic field intensity. 7 6 Iron Recovery (%) 5 4 3 2 1 5 1 15 2 25 3 Pulp Density of the Feed (%) Figure 1 : Graph of Iron Recovery against Pulp Density of the Feed of Kapar Fly Ash Using WHIMS with Magnetic Field Intensity Constant at 8, Gauss 7 6 Iron Recovery (%) 5 4 3 2 1 2, 4, 6, 8, 1, 12, Magnetic Field Intensity (Gauss) Figure 2 : Graph of Iron Recovery of Kapar Fly Ash Samples as a Function of Magnetic Field Intensity Using WHIMS with Pulp Density Constant at 2% Mineral Transformation During Hydrothermal Treatment Mineral transformation during hydrothermal treatment was studied by means of the XRD diffraction patterns. The relative intensities of the diffraction patterns of the two major fly ash crystalline phases, quartz and mullite, and synthetic zeolite formed (zeolite P), were measured at various reaction temperatures and reaction times. The results are presented in Figures 3 to 7. 19

Solid State Science and Technology, Vol. 16, No 1 (28) 17-113 ISSN 128-7389 1 9 8 7 6 5 4 3 2 1 36 32 28 24 2 16 12 8 4 Cation Exchange Capacity (meq/1g) Figure 3 : Relative Intensities of XRD Reflections of Major Crystalline Phases and Values against Reaction Time for Hydrothermal Treatment at 7 C 1 9 8 7 6 5 4 3 2 1 36 32 28 24 2 16 12 8 4 Cation Exchange Capacity (meq/1g) Figure 4 : Relative Intensities of XRD Reflections of Major Crystalline Phases and Values against Reaction Time for Hydrothermal Treatment at 8C 11

Solid State Science and Technology, Vol. 16, No 1 (28) 17-113 ISSN 128-7389 1 9 8 7 6 5 4 3 2 1 36 32 28 24 2 16 12 8 4 Cation Exchange Capacity (meq/1g) Figure 5 : Relative Intensities of XRD Reflections of Major Crystalline Phases and Values against Reaction Time for Hydrothermal Treatment at 9C 1 9 8 7 6 5 4 3 2 1 36 32 28 24 2 16 12 8 4 Cation Exchange Capacity (meq/1g) Figure 6 : Relative Intensities of XRD Reflections of Major Crystalline Phases and Values against Reaction Time for Hydrothermal Treatment at 1C 111

Solid State Science and Technology, Vol. 16, No 1 (28) 63-74 ISSN 128-7389 The mineral transformation phenomena observed in this study were consistent with the result of previous studies [4-5]. Alkali medium was always found to dissolve the aluminosilicate glass and the dissolution rate of silica was accelerated more than that of alumina by increasing temperature and reaction time. This is because mullite was more stable and more difficult to dissolve in comparison to quartz. The subsequent formation of synthetic zeolites rapidly consumed the dissolved species to feed the crystal growth crystallization of zeolite P which produce the highest value, as when Kapar fly ash was treated with NaOH at 7 C at a reaction time of 48 hours. In this stage, almost all the zeolite P produced is from the dissolution of aluminosilicate glass. The dissolution of impurities from fly ash is also a minimum in this stage and, therefore, the zeolite produced is almost purely from aluminosilicate material. The prolonged reaction time of 48 hours at 7 C and increasing hydrothermal reaction temperature to more than 7 C produced synthetic zeolite P from the dissolution of aluminosilicate glass, quartz, mullite and impurities in Kapar fly ash. The lower value in this stage was probably due to a desilication process, in which the silica and alumina dissolved by the alkali reaction were reprecipitated and formed a sodiumaluminum silicate desilication product [6]. In this stage also, a lot of impurities from fly ash dissolved in the solution because of increase of reaction time and temperature. The results agree with findings by many researchers [7-8] which show that prolonged reaction time and increasing temperature frequently result in contamination of zeolite product with undesirable elements such as Fe, Ti and Mn. These elements were thought to be present as soluble oxides in the coal fly ash and were expected to form oxy-anions upon dissolution under alkaline conditions. Jansen [9] has shown that the presence of impurities may affect the crystal form and chemical properties of the zeolite formed. While Inglezakis et al. [1] showed that the decreased of in zeolite was due to surface dust such as precipitated salts and other impurities clogging part of the pore openings in the zeolite structure. Therefore, it is probably that incorporation of these impurities during crystallization of zeolite may in some way affect the values of zeolite P. Chang and Shih [11] also explain that with increasing temperature and reaction time, there is a possibility of ion exchange of impurities occurring in the samples with Na+ ions in the zeolites. CONCLUSION The following main conclusions are obtained from the results of this study: Magnetic separation was successful in removing iron from Kapar fly ash, considered to be deleterious to the zeolite formation process. Optimum separation conditions were achieved with 2% pulp density and 8,7 Gauss (.87 Tesla) magnetic field intensity, with the removal efficiency of iron around 62%. Mineral transformation during hydrothermal treatment was studied by means of the XRD diffraction patterns with values. The initial mineral 112

Solid State Science and Technology, Vol. 16, No 1 (28) 63-74 ISSN 128-7389 transformation phenomenon was the dissolution of aluminosilicate glass in the sample and subsequent formation of synthetic zeolite P. Prolonged reaction time greater than 48 hours at 7 C and hydrothermal temperature greater than 7 C dissolved aluminosilicate glass, quartz, mullite and impurities from Kapar fly ash. The dissolution of these minerals consequently produced contamination in the synthetic zeolite P product with undesirable elements such as Fe, Ti and Mn. The presence of these impurities resulted in lowering the value of synthetic zeolite P. REFERENCES [1]. M. Murat, (1992); Clays Minerals, 27, 119-13. [2]. W. J. Ball, (1986); Proceeding of Seventh International Zeolite Conference, Tokyo, Japan, 137-144. [3]. R. T. Hemmings, E. E. Berry, B. J. Cornelius and B. E. Scheetz, (1986); Fly Ash and Coal Conversion By-Products: Characterization, Utilization and Disposal III, Material Research Society, Boston, USA. [4]. A. Singer and V. Bergaut, (1995); Journal of Environmental Science and Technology, 29, 1748-1753. [5]. X. Querol, N. Moreno, J. C. Umana, A. Alastuey and E. Hernandez,(22); International Journal of Coal Geology, 5, 413-423. [6]. N. M. Rice and J. M. Noone, (1984); Proceeding of ASHTEC 84 Second International Conference on Ash Technology and Market, London, UK, 253-261 [7]. M. Tassopoulos and R. W. Thompson, (1987); Zeolites, 7,243-248. [8]. K. S. Hui and C. Y. H. Chao. (25); Microporous Mesoporous Materials, 88, 145-151. [9]. J. C. Jansen, (21); Introduction to Zeolite Science and Practice, Elsevier, Amsterdam, Netherlands [1]. V. J. Inglezakis, K. J. Hadjiandreou, M. D. Loizidou and H. P. Grigoropoulou, (21); Water Research, 35, 2161-2166. [11]. H. L. Chang and W. H. Shih, (1995); Ceramic Translation, 61, 81-88, 113