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보고서 요약서
요약문
SUMMARY
Contents
목차
제1장 연구개발과제의 개요 25
제1절 기술의 개요 25
제2절 연구개발의 필요성 28
제2장 국내외 기술개발 현황 34
제1절 선광/분체 기술 조사 및 현황 34
제2절 구리광의 일반현황 42
제3절 중저품위 비금속광물 분체화 기술 58
제4절 사용 후 연료 정제 및 기능성 재료개발 59
제3장 연구개발수행 내용 및 결과 61
제1절 금속광의 선별기술 개발 61
제2절 저에너지 탈수/건조 및 고도 해쇄 Mechanism 개발 79
제3절 중저품위 비금속광물 분체화 (백색도 향상포함) 96
제4절 사용 후 연료 정제 및 기능성 재료개발 109
제4장 목표달성도 및 관련분야에의 기여도 140
제5장 연구개발결과의 활용계획 141
제1절 연구성과 141
제2절 연구 성과의 활용방안 144
제6장 연구개발과정에서 수집한 해외과학기술정보 146
제1절 산업광물의 선진선광기술 146
제7장 참고문헌 177
Table 2-1. Special quality of copper 43
Table 2-2. Main form of copper mine 45
Table 2-3. Purpose of copper 46
Table 2-4. Purpose of copper concentrate 47
Table 2-5. Reserve and grade of Copper ore in domestic 48
Table 2-6. Demand and supply results of copper ore in domestic 49
Table 2-7. Import status of iron ore by nations 49
Table 2-8. Reserve & reserve base of iron ore in the world 50
Table 3-1. Chemical analysis(ICP) of jambi mine copper minerals used in this study 62
Table 3-2. Chemical analysis(XRF) of jambi mine copper minerals used in this study 62
Table 3-3. Size distribution and chemical analysis of various size fraction for copper minerals from Jambi mine 63
Table 3-4. Major chemical composition of Jindo porelain stone ore (wt%) 99
Table 3-5. Wet sieving results of ore crushed by a cone crusher with dry sieving 100
Table 3-6. Wet sieving results of ore ground by a ball mill for 5 min 101
Table 3-7. Wet sieving results of ore ground by a ball mill for 10 min 101
Table 3-8. Wet sieving results of ore ground by a ball mill for 15 min 102
Table 3-9. Wet sieving results of ore ground by a ball mill for 20 min 102
Table 3-10. Fe content of the fractions with various intensity of magnetic field 104
Table 3-11. Fe content of the fractions magnetically separated with various number of stages 105
Table 3-12. Comparison Between Pulverized Coal Combustion (PCC) and Fluidized Bed Combustion (FBC) (Botha, 2004) 111
Table 3-13. Comparison of coal combustion conditions in the Donghae and Seochun power station 111
Table 3-14. Experimental parameters of the NaOH concentration, the curing time, and the temperature for manufacturing geopolymers 116
Table 3-15. Weight percentage of Donghae bottom ash separated on sieves and proximate analysis results of each fraction 118
Table 3-16. Weight percentage of Donghae bottom ash separated on sieves after rod milling for 5 min 120
Table 3-17. Weight percentage of Donghae bottom ash separated on sieves after rod milling for 10 min 121
Table 3-18. Weight percentage of Donghae bottom ash separated on sieves after rod milling for 15min 121
Table 3-19. Weight percentage of Donghae bottom ash separated on sieves after rod milling for 20 min 122
Table 3-20. Proximate analysis results of flotation products after rod milling 123
Table 3-21. Proximate analysis results for bottom ashes (wt%) 125
Table 3-22. Proximate analysis results of flotation products from Donghae bottom ash. After two stages of scavenger, the carbon content was reduced to 0.00wt% in the cleaned ash 129
Table 3-23. Chemical composition of the cleamed bottom ash sample from the Donghae power station 132
Table 3-24. Compressive strength of the compression bodies from the cleaned Donghae bottom ash cured at ambient temperature 133
Table 3-25. Compressive strength of the compression bodies from the cleaned Donghae bottom ash cured at 60℃ 135
Table 3-26. Compressive strength of the compression bodies from the cleaned Donghae bottom ash cured at 80℃ 136
Table 3-27. BET-specific surface area of carbon separated from Donghae bottom ash and activated by KOH 138
Fig. 1-1. A diagram presenting the research structure. 26
Fig. 1-2. Suggested research strategies. 27
Fig. 1-3. Secure ratio of metal minerals by year in Korea. 29
Fig. 1-4. Import amount of metal minerals by year of Korea. 30
Fig. 1-5. Import money of metal minerals by year of Korea. 30
Fig. 1-6. Contribution of the research project to KIGAM's mission and national policies. 33
Fig. 2-1. Patent analysis result of mineral processing technologies in chronological order and nationality of the patent holder. 34
Fig. 2-2. Share of the patented mineral processing technologies. 35
Fig. 2-3. Mineral processing technologies in various countries. 36
Fig. 2-4. Patent analysis result of powder technologies in chronological order and nationality of the patent holder. 37
Fig. 2-5. Number of patents on powder technologies in various countries. 37
Fig. 2-6. Share of the patented powder technologies. 38
Fig. 2-7. Number of research papers on mineral processing technologies. 39
Fig. 2-8. Number of research papers on each core technology in mineral processing. 39
Fig. 2-9. Number of research papers on each core technology in mineral processing in chronological order. 41
Fig. 2-10. International price of copper ore by year. 51
Fig. 2-11. Magnetic separator for separation of fine ferruginous minerals. 53
Fig. 2-12. Contact angle between bubble and particle. 54
Fig. 2-13. Flotator used in this test for froth flotation of copper ore. 55
Fig. 2-14. Principle and schematic view of froth flotation. 56
Fig. 2-15. Principle and schematic view of column flotation. 57
Fig. 3-1. XRD analysis of raw copper sample from Indonesia Zambi. 61
Fig. 3-2. Mapping of raw copper minerals by SEM-EDAX 63
Fig. 3-3. Flowsheet for froth flotation of copper minerals 64
Fig. 3-4. Effect of magnet intensity on grade & recovery of Cu in wet-magnetic separation 66
Fig. 3-5. Effect of dosage of collector on grade and recovery of copper in froth flotation. 67
Fig. 3-6. Effect of pH on grade & recovery of copper in froth flotation 68
Fig. 3-7. Effect of kinds of collector on grade & recovery of copper in froth flotation 69
Fig. 3-8. Grade and recovery of Ag and copper sulfide in froth flotation 70
Fig. 3-9. Effect of dosage of collector on grade and recovery of copper in froth flotation 71
Fig. 3-10. Effect of pH on grade & recovery of copper in froth flotation 72
Fig. 3-11. Effect of cleaning time on grade & recovery of copper in froth flotation. 73
Fig. 3-12. Effect of dosage of frother on grade & recovery of copper in froth flotation. 74
Fig. 3-13. Grade and recovery of final concentrates separated from froth flotation. 75
Fig. 3-14. Photo of all products separated from froth flotation. 76
Fig. 3-15. SEM/EDAX(×500) on raw copper minerals (-150mesh). 77
Fig. 3-16. SEM/EDAX(×500) on final concentrate (-150mesh). 77
Fig. 3-17. Attraction and repulsive forces between stabilized colloidal particles. 80
Fig. 3-18. Attraction and repulsive forces between unstable colloidal particles. 81
Fig. 3-19. Basic principles of zeta potential. 82
Fig. 3-20. Electric double layer model. 83
Fig. 3-21. Fundamental principle of micro bubbled slurry. 83
Fig. 3-22. Schematic diagram for the economical disagglomeration process in the study. 84
Fig. 3-23. Compressive strength machine. 85
Fig. 3-24. Kaolin clay slurry by the addition of a surfactant. 86
Fig. 3-25. Micro bubbled cream made by aeration. 87
Fig. 3-26. Slurry samples consisting of two different clays. 87
Fig. 3-27. Facilities for wet disagglomeration. 88
Fig. 3-28. Particle size distribution of raw sample. 88
Fig. 3-29. Drying efficiency of slurries. 89
Fig. 3-30. Drying with Improved efficiency. 90
Fig. 3-31. Pore size in the surface of completely dried slurries. 91
Fig. 3-32. Pore size controlled by the amount of additives. 92
Fig. 3-33. Compressive strength variation in terms of the amount of additives. 92
Fig. 3-34. Efficiency of disagglomeration in D50 particle size.(이미지참조) 93
Fig. 3-35. Efficiency of disagglomeration in D90 particle size.(이미지참조) 94
Fig. 3-36. Particle size distribution curves of disagglomerated particles treated with different surfactants. 95
Fig. 3-37. Cumulative size distribution of disagglomerated particles treated with different surfactants. 95
Fig. 3-38. Experimental condition for Fe removal process from a porcelain stone. 98
Fig. 3-39. X-ray diffraction pattern of porcelain stone produced in Jin Island. 99
Fig. 3-40. Fe₂O₃ content of the non-magnetic fraction with various top particle size. 103
Fig. 3-41. Fe₂O₃ content of the non-magnetic fraction with various top particle size. 104
Fig. 3-42. Fe₂O₃ content of the non-magnetic fraction with various number of stages. 106
Fig. 3-43. Fe₂O₃ content of a porcelain stone produced by selective leaching of Fe with HCl. 106
Fig. 3-44. Fe₂O₃ content of a porcelain stone produced by selective leaching of Fe with H₂SO₄. 107
Fig. 3-45. Whiteness of a purified porcelain stone with HCl. 108
Fig. 3-46. Whiteness of a purified porcelain stone with H₂SO₄. 108
Fig. 3-47. Location map of some domestic power stations. 110
Fig. 3-48. Ash storage pond in Seochun power station. 114
Fig. 3-49. Ash storage pond in Donghae power station. 114
Fig. 3-50. Schematic process flow sheet for the synthesis of geopolymer from FBC bottom ash. 115
Fig. 3-51. Froth flotation circuit for the unburned carbon separation. 115
Fig. 3-52. A tailor-made furnace used for activation of unburned carbon. 116
Fig. 3-53. Compression body prepared for measuring compressive strength. 117
Fig. 3-54. Weight percentage in the size fractions with accumulated bar plot. 119
Fig. 3-55. X-ray diffraction pattern of bottom ash sample from the Donghae power plant. 124
Fig. 3-56. X-ray diffraction pattern of bottom ash sample from the Seochun power station. 125
Fig. 3-57. Heat values in size fractions of Donghae bottom ash. 126
Fig. 3-58. Flotation performance of Donghae bottom ash with varying dosage of kerosene. 127
Fig. 3-59. Flotation performance with varying dosage of pine oil. 127
Fig. 3-60. (a) Cleaned ash and (b) the carbon concentrate prepared from Donghae bottom ash. 128
Fig. 3-61. SEM micrographs of a carbon particle separated from Donghae bottom ash: (a) secondary electron image and (b) back-scattered electron image. 128
Fig. 3-62. Carbon contents of the bottom ash size factions. 130
Fig. 3-63. Carbon contents of the carbon concentrates at various dosages of a collector, kerosene. 131
Fig. 3-64. Carbon contents of the carbon concentrates at various dosages of a frother, pine oil. 131
Fig. 3-65. Scanning electron micrographs of carbon particles separated from the (a) Donghae and (b) Seochun bottom ashes. 132
Fig. 3-66. Compressive strength of the compression bodies from the cleaned Donghae bottom ash cured at ambient temperature. 134
Fig. 3-67. Compressive strength of the compression bodies from the cleaned Donghae bottom ash cured at 60℃. 135
Fig. 3-68. Compressive strength of the compression bodies from the cleaned Donghae bottom ash cured at 80℃. 136
Fig. 3-69. X-ray diffraction pattern of the geopolymer reacted with 8M NaOH solution and cured at 60℃ for 14 days. 137
Fig. 3-70. SEM micrographs of an unburned carbon sample (DBM-F-C-8) activated with (a) 10㎖ and (b) 20㎖ of 45wt% KOH solution. 139
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