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Excessive supply of phosphorus (P), a vital macronutrient for all organisms, can cause unwanted environmental consequences such as eutrophication. An increase in agricultural and industrial activities has created a considerable imbalance in the P cycle with continuing adverse effects on sustainability and ecosystem health, thereby stipulating/postulating the significance of P removal. However, it is challenging for conventional P removal technologies to remove both high and low concentration of P efficiently and economically from aqueous solution. Therefore, in the present study a unique and sustainable concept for the removal of P through the utilization of waste bivalve seashells was proposed.
Continuous dumping of seashells in open fields has been a global issue, causing serious problems in the water and human health. The conversion of those wastes into value-added products is highly desirable. Here, nano-calcium hydroxide (N-CH) were first synthesized from waste seashells by a chemical precipitation method in an aqueous medium at 90 °C without using any additives. The crystal structure with a hexagonal portlandite [Ca(OH)2], crystal size of around 100?400 nm, and specific surface area with 4.96 m2 g-1 were confirmed. In addition, a schematically organized new qualitative model for a mechanism was proposed to explain the genesis and evolution of N-CH from raw seashells. Furthermore, experimental results revealed successful removal of high concentration of P (> 20 mg L-1) from aqueous solution from N-CH synthesized from various type of seashell with similar P removal efficiencies of ~ 97 %. An optimization study has been conducted using the Box?Behnken design of response surface methodology, which highlights that with a calcium/phosphorus mass ratio, pH, and temperature of 2.16, 10.2, and ~ 25 °C respectively, a P removal efficiency of 99.33% can be achieved in a residence time of 10 min. Also, under the same conditions, diluted human urine was analyzed and P removal efficiency of ∼ 95 % was observed. Through experimental results, semiquantitative phase analysis, and transmission electron microscopy, it has been found that the reaction was diffusion-controlled, which was further confirmed through shrinking core diffusion modeling. The present study manifests the promising potential of waste seashell-derived nano-calcium hydroxide for phosphorus treatment and its precipitation in the form of value-added hydroxyapatite.
Even in low P concentration (≤ 1 mg L-1), P can be detrimental for ecosystem’s health, but this aspect has not been thoroughly investigated. The elimination of low P content is rather expensive or complex. Therefore, a sustainable method has been proposed in which valorized bivalve seashells can be used for the removal of low P content. Initially, acicular shaped aragonite particles (~ 21 μm) with an aspect ratio of around 21 have been synthesized through the wet carbonation process. Also, a schematic crystal growth mechanism was proposed to demonstrate the genesis and progression of aragonite crystal. Green aragonite can bridge the void for numerous applications and holds the potential for the commercial-scale synthesis with bivalve seashells as low-cost precursors. Green aragonite were then subsequently used to treat aqueous solutions containing P in low concentration (P ≤ 1 mg L-1). Response surface methodology-based Box-Behnken design has been employed for optimization study which revealed that with aragonite dosage (140 mg), equilibrium pH (~ 10.15), and temperature (45 ℃), a phosphorus removal efficiency of ~ 97 % can be obtained in 10 h. The kinetics and isotherm studies have also been carried out (within the range P ≤ 1 mg L-1) to investigate a probable removal mechanism. Also, aragonite demonstrates higher selectivity (> 70 %) towards phosphate with coexisting anions such as nitrate, chloride, sulfate, and carbonate. Through experimental data, elemental mapping, and molecular dynamic simulation, it has been observed that the removal mechanism involved a combination of electrostatic adsorption of Ca2+ ions on aragonite surface and chemical interaction between the calcium and phosphate ions. The present work demonstrates a sustainable and propitious potential of seashell derived aragonite for the removal of low P content in aqueous solution along with its unconventional mechanistic approach.
Continuous dumping of seashells in open fields has been a global issue, causing serious problems in the water and human health. The conversion of those wastes into value-added products is highly desirable. Here, nano-calcium hydroxide (N-CH) were first synthesized from waste seashells by a chemical precipitation method in an aqueous medium at 90 °C without using any additives. The crystal structure with a hexagonal portlandite [Ca(OH)2], crystal size of around 100?400 nm, and specific surface area with 4.96 m2 g-1 were confirmed. In addition, a schematically organized new qualitative model for a mechanism was proposed to explain the genesis and evolution of N-CH from raw seashells. Furthermore, experimental results revealed successful removal of high concentration of P (> 20 mg L-1) from aqueous solution from N-CH synthesized from various type of seashell with similar P removal efficiencies of ~ 97 %. An optimization study has been conducted using the Box?Behnken design of response surface methodology, which highlights that with a calcium/phosphorus mass ratio, pH, and temperature of 2.16, 10.2, and ~ 25 °C respectively, a P removal efficiency of 99.33% can be achieved in a residence time of 10 min. Also, under the same conditions, diluted human urine was analyzed and P removal efficiency of ∼ 95 % was observed. Through experimental results, semiquantitative phase analysis, and transmission electron microscopy, it has been found that the reaction was diffusion-controlled, which was further confirmed through shrinking core diffusion modeling. The present study manifests the promising potential of waste seashell-derived nano-calcium hydroxide for phosphorus treatment and its precipitation in the form of value-added hydroxyapatite.
Even in low P concentration (≤ 1 mg L-1), P can be detrimental for ecosystem’s health, but this aspect has not been thoroughly investigated. The elimination of low P content is rather expensive or complex. Therefore, a sustainable method has been proposed in which valorized bivalve seashells can be used for the removal of low P content. Initially, acicular shaped aragonite particles (~ 21 μm) with an aspect ratio of around 21 have been synthesized through the wet carbonation process. Also, a schematic crystal growth mechanism was proposed to demonstrate the genesis and progression of aragonite crystal. Green aragonite can bridge the void for numerous applications and holds the potential for the commercial-scale synthesis with bivalve seashells as low-cost precursors. Green aragonite were then subsequently used to treat aqueous solutions containing P in low concentration (P ≤ 1 mg L-1). Response surface methodology-based Box-Behnken design has been employed for optimization study which revealed that with aragonite dosage (140 mg), equilibrium pH (~ 10.15), and temperature (45 ℃), a phosphorus removal efficiency of ~ 97 % can be obtained in 10 h. The kinetics and isotherm studies have also been carried out (within the range P ≤ 1 mg L-1) to investigate a probable removal mechanism. Also, aragonite demonstrates higher selectivity (> 70 %) towards phosphate with coexisting anions such as nitrate, chloride, sulfate, and carbonate. Through experimental data, elemental mapping, and molecular dynamic simulation, it has been observed that the removal mechanism involved a combination of electrostatic adsorption of Ca2+ ions on aragonite surface and chemical interaction between the calcium and phosphate ions. The present work demonstrates a sustainable and propitious potential of seashell derived aragonite for the removal of low P content in aqueous solution along with its unconventional mechanistic approach.
목차
- ACKNOWLEDGEMENT iABSTRACT iv국문 초록 viiiABBREVIATIONS xiList of Tables xviiiList of Figures xxChapter 1. Introduction 1-241.1. Problem Description 11.1.1. Phosphorus: An Exhaustible Resource 11.1.2. Environmental Concerns 21.1.3. Current Phosphorus Removal Technologies 21.1.4. Environmental Concerns Regarding Waste Bivalve Seashells 41.2. Research Gap 41.3. Research Hypothesis 51.4. Research Aim and Objectives 61.5. Research Significance 71.6. Thesis Outline 81.7. Literature Review 91.7.1. Phosphorus Life Cycle 91.7.1.1. Primary Source 91.7.1.2. Land-ocean-biota Transfer 101.7.1.3. Human Alteration in the Phosphorus Cycle 111.7.2. Eutrophication 121.7.3. Phosphorus Removal Technologies 141.7.4. Waste Bivalve Seashells: A Potential Calcium Supplement 171.7.4.1. Environmental Concerns Regarding Bivalve Seashells 171.7.4.2. Valorization of Bivalve Seashells 181.7.4.3. Eco-friendly Calcium-based Nanoparticles 181.7.4.4. Bivalve seashell derived nano-calcium hydroxide particles 191.7.4.5. Bivalve Seashell Derived Green Aragonite Particles 201.7.5. Potential of calcium-based nanoparticles for Phosphorus treatment 211.7.6. Strategic Utilization of Carbon Dioxide 23Chapter 2. Research Methodology 25-352.1. Materials 252.2. Synthesis of Calcium Based Particle 262.2.1. Nano-calcium Hydroxide 262.2.2. Synthesis of Green Aragonite Particles 272.3. Test Method 292.3.1. High Concentration Phosphorus Removal Batch Experiments: Chemical Precipitation 292.3.2. Low Concentration Phosphorus Removal Batch Experiments: Sorption 302.4. Chemical Analysis 312.5. Optimization Through Response Surface Methodology 322.6. Crystalline Characteristics 332.6.1. X-ray Diffraction 332.6.2. Fourier Transform Infrared Spectroscopy 332.6.3. Brunauer?Emmett?Teller 342.6.4. Field Emission Scanning Electron Microscopy 342.6.5. Transmission Electron Microscopy 34Chapter 3. Removal of Phosphorus in Aqueous Solution by Nano-calcium Hydroxide Derived from Waste Bivalve Seashells: Mechanism and Kinetics 36-753.1. Result and Discussion 363.1.1. Physicochemical Characterization of Synthesized Nano-calcium Hydroxide 363.1.2. Mechanism Study 473.1.3. Precipitation Performance of Phosphorus 503.1.3.1. Optimization Through the Box-Behnken Methodology 553.1.3.2. Mechanism and Kinetic Studies 683.2. Conclusion 75Chapter 4. Low Concentrated Phosphorus Sorption in Aqueous Medium on Aragonite Derived by Carbonation of Seashells Optimization, Kinetics, and Mechanism Study 76-1124.1. Result and Discussion 764.1.1. Physicochemical Characterization of Aragonite 764.1.1.1. X-ray Diffraction 764.1.1.2. Fourier Transform Infrared Spectroscopy 774.1.1.3. Scanning Electron Microscopy 794.1.1.4. Brunauer-Emmett-Teller 814.1.2. Performance of Phosphorus Sorption 834.1.2.1. Optimization Study 844.1.2.2. Kinetics and Isotherm Studies 974.1.2.3. Effect of Competing Ions 1054.1.2.4. Mechanism Study 1064.2. Conclusion 112Chapter 5. Conclusion 113-116Chapter 6. Future Prospects 117-1216.1 Future Research on Nano-calcium Hydroxide 1176.2. Exploration of N-CH Applications 1186.3. Role of N-CH in Marine Phosphorus Burial 1186.4. Future Research on Green Aragonite 1196.5. Exploration of Green Aragonite Applications 1206.6. Synthesis of Green Aragonite from Seawater 120REFERENCES 122ACHIEVEMENTS 146