TW201245102A - Method of fabricating aluminum-dross imitation stone composite - Google Patents
Method of fabricating aluminum-dross imitation stone composite Download PDFInfo
- Publication number
- TW201245102A TW201245102A TW100116924A TW100116924A TW201245102A TW 201245102 A TW201245102 A TW 201245102A TW 100116924 A TW100116924 A TW 100116924A TW 100116924 A TW100116924 A TW 100116924A TW 201245102 A TW201245102 A TW 201245102A
- Authority
- TW
- Taiwan
- Prior art keywords
- artificial stone
- slag
- aluminum
- composite material
- stone composite
- Prior art date
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 136
- 238000004519 manufacturing process Methods 0.000 title claims description 30
- 239000004575 stone Substances 0.000 title abstract description 18
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 77
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 77
- 238000003723 Smelting Methods 0.000 claims abstract description 41
- 239000002699 waste material Substances 0.000 claims abstract description 38
- 239000000463 material Substances 0.000 claims abstract description 27
- 239000002969 artificial stone Substances 0.000 claims description 119
- 239000002893 slag Substances 0.000 claims description 91
- 239000002518 antifoaming agent Substances 0.000 claims description 29
- 238000007670 refining Methods 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 28
- 239000002994 raw material Substances 0.000 claims description 26
- 239000011347 resin Substances 0.000 claims description 21
- 229920005989 resin Polymers 0.000 claims description 21
- 238000004064 recycling Methods 0.000 claims description 14
- 239000004848 polyfunctional curative Substances 0.000 claims description 10
- 238000000465 moulding Methods 0.000 claims description 8
- 239000011268 mixed slurry Substances 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 5
- 238000012545 processing Methods 0.000 claims description 5
- 229920001187 thermosetting polymer Polymers 0.000 claims description 5
- 238000005266 casting Methods 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 238000005192 partition Methods 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 3
- 229920006337 unsaturated polyester resin Polymers 0.000 claims description 3
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical group OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 claims description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical group CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 claims 1
- 230000005484 gravity Effects 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- 239000000428 dust Substances 0.000 abstract description 21
- 230000007613 environmental effect Effects 0.000 abstract description 7
- 238000011084 recovery Methods 0.000 abstract description 3
- 238000005299 abrasion Methods 0.000 abstract 1
- 239000003963 antioxidant agent Substances 0.000 abstract 1
- 230000003078 antioxidant effect Effects 0.000 abstract 1
- 235000006708 antioxidants Nutrition 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 52
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 238000010586 diagram Methods 0.000 description 17
- 239000000047 product Substances 0.000 description 17
- 230000008569 process Effects 0.000 description 15
- 238000010521 absorption reaction Methods 0.000 description 11
- 238000005452 bending Methods 0.000 description 11
- 239000000284 extract Substances 0.000 description 10
- 239000000843 powder Substances 0.000 description 9
- 239000013530 defoamer Substances 0.000 description 7
- 229910001385 heavy metal Inorganic materials 0.000 description 7
- 239000002002 slurry Substances 0.000 description 7
- 238000009933 burial Methods 0.000 description 6
- 230000008929 regeneration Effects 0.000 description 6
- 238000011069 regeneration method Methods 0.000 description 6
- 239000004566 building material Substances 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000013461 design Methods 0.000 description 4
- 238000001514 detection method Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000005065 mining Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000007790 solid phase Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000002860 competitive effect Effects 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000012779 reinforcing material Substances 0.000 description 2
- 239000011435 rock Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000011669 selenium Substances 0.000 description 2
- 238000005728 strengthening Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 230000003313 weakening effect Effects 0.000 description 2
- 241000272525 Anas platyrhynchos Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- -1 Ketone Peroxide Chemical class 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000000809 air pollutant Substances 0.000 description 1
- 231100001243 air pollutant Toxicity 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003064 anti-oxidating effect Effects 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- MMCOUVMKNAHQOY-UHFFFAOYSA-N carbonoperoxoic acid Chemical compound OOC(O)=O MMCOUVMKNAHQOY-UHFFFAOYSA-N 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical compound [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000010438 granite Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000010982 man-made stone Substances 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 238000010309 melting process Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 230000003716 rejuvenation Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 230000022676 rumination Effects 0.000 description 1
- 208000015212 rumination disease Diseases 0.000 description 1
- 229910001925 ruthenium oxide Inorganic materials 0.000 description 1
- WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 description 1
- 239000000366 soil substitute Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- 238000009849 vacuum degassing Methods 0.000 description 1
Landscapes
- Processing Of Solid Wastes (AREA)
Abstract
Description
201245102 六、發明說明: 【發明所屬之技術領域】 本發明係有關於一種煉鋁爐渣人造石複合材料之製造方 法’尤指涉及一種可以製造出具有高附加價值之人造石複合材 料’特別係指採用廢鋁再生冶煉過程所產生之煉鋁浮渣與集塵 灰為原料,於常溫下達成廢棄物資源再利用之目的。 【先則技術】 廢铭再生冶煉之技術,在國内大部份之廠商最常使用小型 反射爐(1.5〜7.5嘴/天),將所收集到之廢料,先依其合金種 類成份加以區分,再加以炫煉後而製作鋁贫(林偉凯、蔡潔娃 ’『金屬資源再生產業技術發展概況分析』,金屬中心,2〇〇9) 。而廢鋁再生原料通常可分為新廢料及舊廢料兩種,新廢料為 煉鋁製造程序中所產生之邊材、鋁渣及不合格產品’其數量佔 再生鋁70 wt%左右,舊廢料則為使用過之鋁製產品如鋁電線 電纜、汽車車身組件與鑄品、鋁罐、及家電製品。 廢紹再生冶煉之公害污染較少,溶煉再生過程產生之副產 物主要為煉銘爐渣,煉銘爐渣包括煉銘浮渣(Dross)與煉鋁 集塵灰。在紹鱗邊業之溶煉製程’包含溶化紹製程、回收銘液 製程或冷卻製程等所產生之廢氣中,含有懸浮微粒之空氣污染 物,這些污染物可藉由袋濾式集塵器之空氣污染防制設備加以 收集,其所收集之煉鋁集塵灰,通常稱為白灰(whitedust)( Murayama, N., Shibata, J., Sakai, K., Nakajima, S. and201245102 VI. Description of the Invention: [Technical Field of the Invention] The present invention relates to a method for manufacturing an aluminum slag slag artificial stone composite material, particularly to an artificial stone composite material capable of producing high added value. The aluminum scum and dust ash produced by the waste aluminum refining process are used as raw materials to achieve the purpose of recycling waste resources at room temperature. [First-class technology] The technology of waste re-smelting and smelting, most of the domestic manufacturers often use small reverberatory furnaces (1.5~7.5 mouths/day), and the collected wastes are first distinguished according to their alloy components. After further tempering, the production of aluminum is poor (Lin Weikai, Cai Jiewa's "Analysis of the development of metal resources recycling industry technology", Metal Center, 2〇〇9). The waste aluminum recycling raw materials can be generally divided into new waste and old waste. The new waste is the sapwood, aluminum slag and unqualified products produced in the aluminum smelting manufacturing process. The quantity accounts for about 70 wt% of recycled aluminum, and the old waste It is used aluminum products such as aluminum wire and cable, automotive body components and castings, aluminum cans, and home appliances. The waste pollution of waste smelting and refining is less, and the by-products produced by the refining and refining process are mainly smelting slag, and the refining slag includes Dross and aluminum ash. In the smelting process of the Shaobianbian industry, the exhaust gas generated by the melting process, the recovery process or the cooling process contains air pollutants of suspended particles, which can be filtered by a bag filter. The air pollution control equipment is collected and collected from the aluminum dust collection ash, usually called whitedust (Murayama, N., Shibata, J., Sakai, K., Nakajima, S. and
Yamamoto, H., Synthesis of hydrotalcite-like materials from - ' . . various wastes in aluminum regeneration prQcess”,Resource 201245102Yamamoto, H., Synthesis of hydrotalcite-like materials from - ' . . various wastes in aluminum regeneration prQcess", Resource 201245102
Processing 53, pp.6-11,2006)或銘二級冶煉程序集塵灰(即煉 鋁集塵灰)。煉鋁集塵灰之產量約為原廢鋁再生冶煉量之1 wt% ’主要成份為氧化鋁(Al2〇3)與氧化鎂(MgO)及碳( .碳之來源為熔煉時使用之重油燃料)。另外’熗煉製程中亦產 生煉鋁浮渣,煉鋁浮渣大部份漂浮於熔融鋁湯上面,主要由金 屬銘與IS之氧化物及氮化物所組成,其產生量視原料而定,約 為原廢铭溶煉量之15 wt%。煉銘爐渣副產物無論係煉銘浮渣 或煉銘集塵灰,因其都含有銘之氮化物,當曝露在空氣中遇潮 或吸濕則會水解(Hydrolysis)產生氨氣,具有強烈之刺鼻味 。目前,煉鋁爐渣若需拋棄或掩埋,必須先加以中和固化等處 理程序(Hermsmeyer,D.,Diekmann,R.,Ploeg R. R. and Horton R” “Physical properties of a soil substitute derived from an aluminum recycling by-product”,Journal of Hazardous Materials B95, pp. 107-124,2002 ; Shinzato, M. C. and Hypolito, R., <4Solid waste from aluminum recycling process: characterization and reuse of its economically valuable eonstituents”,Waste Management 25, ΡΡ·37_46, 2005 ;以及 Murayama,N.,Arimura, K.,Okajima,N. and Shibata,J” “Effect of structure-directing agent on AlP04-n synthesis from aluminum dross", International Journal of Mineral Processing 93, pp.l 10-114, 2009 ) 〇 在國内煉鋁浮渣與集塵灰之處理方式,通常仍以廠内堆置 及掩埋為主,若處理不當仍會對環境造成衝擊,並危害人體健 康。而煉鋁爐渣無論從質與量觀之,都具有相當之經濟價值, 因此從零廢棄與魏翻峨點,應發展纽漏化再生技術 與方法’以達回收再利用煉鋁浮渣與集塵灰之目的。對此,本 201245102 請中華民國第327561號之「水祕岩人造 H方法」發明專利,其係湖廢棄物製成之水泮嫁岩 顆粒為原料而製造出具有高附加價值之水淬絲人造石,雖可 達成廢棄物資源再利用之目的,惟其製程需要在高溫下進行處 理’不僅設備費用高、消耗能源大,且起爐停爐耗時,因而導 ^廢棄物處理成本偏高。故,—般㈣者係無法符合使用者於 實際使用時之所需。 先則中華民國專利當中,人造石複合材料之製造原料如 中華民國第025924號之「具有各種花紋之人造石板」專利係 使,=以及石粉作為人造石原料;而中華民國第號 ,:密度人造石以及其製法」以及中華民國第115373號之 人&石材及其製法」所使用之成份為碳酸氧化紹等I 質細粒。中華民國第1242543號之「人造石壁材」製作喃添 加無機質細粒成分,其來源由制岩献理石等㈣石材壁 磚等成型^所粉碎,並齡級,以及海沙或河沙等砂經分級者 之-種以上。中華民國第娜5744號之「人造石結構改良」 可:獲得高硬度及耐火效果之人造石,需添加石粉作為原料。 如前述人造石複合材料專利所提及之人造石添加物:碎石石粉 氧化紹、無機質細粒、花崗岩或大理石粉碎石粉等,皆為天 然原料。大量使用會增加原物料之開採、對環境造成衝擊與開 採過程之碳排放,.且人造石製造商須負擔原料之成本而練銘 爐渣若有效再利用材料化為人造石複合材料之添加物,則可減 少煉鋁爐渣掩埋處理費用、掩埋後對環境之衝擊、原物料之開 採與製作成本之費用。' 有鑑於台灣因資源有限,更應從煉鋁浮渣與集塵灰之回收s • · 201245102 再利用上,充分發揮資源再生功能,不僅可以解決其可能污染 裱境之問題,亦可替代一般人造石製程上所耗費之原料。因此 發展一套可解決相關環境問題與前案技術缺點之發明實有必 要 〇 ... 【發明内容】 本發明之主要目的係在於,克服習知技藝所遭遇之上述問 題並&供讎用廢I呂再生冶煉過程所產生之煉紹浮潰與集 塵灰為原料,於常溫下製造出具有高附加價值之人造石複& 料,俾以達成廢棄物資源再利用之方法。 本發明之次要目的係在於,提供—歡煉贿麟集塵灰 為顆粒狀強化材料,在複合材料中扮演機械性質之加強者,以 促進人造錢合材权賊強度、硬度及耐舰之方法。 ^發明之另—目的係在於,提供—種以煉銘浮渣與集塵灰 之…、魏化域氧切等辦錯,明加 耐燃與抗氧雛之綠。 I材枓之 資_在於,提^H舰料输煉 料化耥’將之製作成人造石複合 ==產品,並實驗此類人造石複合材料之基本物理化學 “此之又—目的係在於,提供—種降低成本,1能利用 =再生貝源’進一步減少消耗自然資源與破壞 相 备大之環境效益,可推動綠色材料、綠色營建^有相 色資源再生利用之益處之方法。 、、’a產業及綠 201245102 . - .... ...... . ... · . -:. <本發明之又再一目的係在於,提供一種煉鋁浮渣與集塵灰 ’可娜代或齡原來人造石複合材料生產過程, 所需添加之原物料’為以煉鋁浮渣與集塵灰材料化與資源化產 品之方法9 為達以上之目的,本發明係一種煉鋁爐渣人造石複合材料 之製造方法’將廢鋁再生原料經廢鋁再生冶煉處理後所得之煉 =第塵灰,在添加量介於42.5〜64.〇 wt%之範園内與樹脂進行 此拌’同時添加硬化劑、消泡劑與促進劑而攪拌成一混合漿 料’再將該混合漿料洗鑄於成型模具中,於常溫下待其交聯固 化’形成一本體,並進行脫膜,即製得煉鋁爐渣人造石複合材 料。 • .· 【實施方式】 凊參閱『第1圖及第2圖』所示,係分別為本發明之架構 及本發明之製作流程示意圖。如圖所示:本發明係一種 ^罐紅造石複合材料之製造方法’係__再生冶煉過 程所產生之煉紹爐渣為原料,以達成廢棄物資源再利用之目的 ,俾以製造A具有高附加健之人造;5複合觀。該人造石複 合材料1包括-本體’其組成成分包含煉_渣i i、樹脂1 2、靖泡劑13、硬化劑i 4及促進劑!5,係將廢紹再生原 齡雜再生雜處理麟得之聽触,在添加量介於42 5 〜64.0 wt%之範_與樹脂進行混拌,_添加硬化劑、消泡 雜錢綱游成—混合麟,縣魏合倾絲於成型 模具中’於常溫下待其交聯固化成一柄後,進行脫膜,即製 201245102 得-喊型、常溫硬化而呈—縱大小之人造複合材料。其製 .作流知如第2圖所示,係至少包含下列步驟: ⑷製備步驟2 1 :回收廢鋁再生原料,並將該廢鋁再 .生原_廢_生冶煉處理,於絲再生顧產生綠屬冶煉 爐漬(下稱煉紹爐逢)’包括浮渣(Dr〇ss)與煉紹集塵灰,盆 中該浮驗粉销駿,雜粗雛經由猶爐_回收; 細顆粒則與該煉紹集塵灰一同以一粉磨過篩處理進行粉碎、研 磨及過料’柄均—雜ΑλΙ、之触浮轉塵灰粉體,再 將此煉财渣/集塵灰粉體進行粉_存處理作乾_存;以 及 (Β )反應成型步驟2 2 :將上述煉料轉塵灰粉體 加=33J〜61.5 wt%之樹脂與〇〜3 5加%之消泡劑進行配比 汁篁處理後’再添加W5罐之硬化劑與促進劑作掉合處理 成-齡轉’籍歧合祕鱗於—成魏具中進行 鋪裝處理’以作人造石複合材料初纟之成型處理,隨後放置於 ^常溫環境下作最後細之常溫養護處理,使其硬化成型以產 W出人造石複合材料,並待脫膜分離後,再藉由裁切修邊處理 與堆叠儲放處理及研磨拋光等加工程序,獲得一煉輝清人造 石複合材料,並可進—步作為翻性樹脂裝飾板、鱗型板、積 層板、活動隔牆及樹脂板等成品。 上述步驟更包料人抽真空脫料元铸,以介於卜如 分鐘之處理_進—步絲該混合漿射存在之錄。 上述步驟(A)廢銘再生原料係為舊廢紹料,並可為使用 躲魏、汽車車雜件赠品、_絲魏品之銘 201245102 • - . . .... -...... .· . - · · - - - _ :. .- 上述步驟(B )樹脂係為不飽和聚醋樹脂’其密度係介於 U1〜1 · 13 g/cm3之間;硬化劑係為過氧化甲乙裥(Methyl EthylProcessing 53, pp. 6-11, 2006) or Ming secondary smelting process dust ash (ie, aluminum dust collection ash). The output of aluminum ash collection dust is about 1 wt% of the original scrap aluminum smelting amount. The main components are alumina (Al2〇3) and magnesia (MgO) and carbon. The source of carbon is the heavy oil fuel used in smelting. ). In addition, aluminum scum is also produced in the 'smelting process. Most of the aluminum scum floats on the molten aluminum soup. It is mainly composed of metal oxides and oxides and nitrides of IS. The amount of production depends on the raw materials. It is about 15 wt% of the original waste. The by-products of the refining slag slag, whether it is refining the scum or refining the dust, it contains the nitride of Ming, and when exposed to the air, it will hydrolyze to produce ammonia when exposed to moisture or moisture. A pungent smell. At present, if the aluminum slag is to be discarded or buried, it must be neutralized and cured (Hermsmeyer, D., Diekmann, R., Ploeg RR and Horton R) “Physical properties of a soil substitute derived from an aluminum recycling by -product", Journal of Hazardous Materials B95, pp. 107-124, 2002; Shinzato, MC and Hypolito, R., <4Solid waste from aluminum recycling process: characterization and reuse of its economically valuable eonstituents", Waste Management 25, ΡΡ·37_46, 2005; and Murayama, N., Arimura, K., Okajima, N. and Shibata, J” “Effect of structure-directing agent on AlP04-n synthesis from aluminum dross”, International Journal of Mineral Processing 93, Pp.l 10-114, 2009 ) The treatment of aluminum scum and dust ash in China is usually based on stacking and burial in the factory. If it is not handled properly, it will still impact the environment and harm the human body. health. The aluminum slag slag has considerable economic value in terms of both quality and quantity. Therefore, from zero waste and Wei turnaround point, the new leaking regeneration technology and method should be developed to achieve recycling and reuse of aluminum scum and set. The purpose of dust. In this regard, this 201245102 invites the invention patent of the "Water Secret Rock Artificial H Method" of the Republic of China No. 327561, which is made of water-stained rock particles made from lake waste as raw materials to produce water-cured silk with high added value. Stone, although it can achieve the purpose of recycling waste resources, but its process needs to be treated at high temperature. 'Not only equipment costs are high, energy consumption is large, and it takes time to start the furnace, so the waste disposal cost is high. Therefore, the general (4) system cannot meet the needs of the user in actual use. First, among the patents of the Republic of China, the raw materials for the manufacture of artificial stone composite materials such as the "artificial stone slabs with various patterns" of the Republic of China No. 025924, = and stone powder as raw materials for artificial stone; and the Republic of China No.: density artificial The ingredients used in the stone and its preparation method, as well as the people of the Republic of China No. 115373 & stone and its preparation method are I fine particles such as carbonic acid oxide. The "artificial stone wall material" of the Republic of China No. 1242543 is made of inorganic fine-grained components, and its source is crushed by the formation of rock and stone, etc. (4) stone wall bricks, etc., and age-grade, as well as sands such as sea sand or river sand. More than one species of the grader. "Man-made stone structure improvement" of the Republic of China No. 5744: It is possible to obtain artificial stone with high hardness and fire resistance, and it is necessary to add stone powder as a raw material. The artificial stone additives mentioned in the above-mentioned artificial stone composite material patent: crushed stone powder, oxidized soda, inorganic fine particles, granite or marble crushed stone powder, etc., are all natural raw materials. Large-scale use will increase the mining of raw materials, impact on the environment and carbon emissions from the mining process. And the artificial stone manufacturer must bear the cost of the raw materials and train the slag if it is effectively reused as an additive to the artificial stone composite. It can reduce the cost of smelting slag burial treatment, the impact on the environment after burial, and the cost of mining and manufacturing of raw materials. In view of Taiwan's limited resources, it should be recycled from aluminum scum and dust collection s • · 201245102 Reuse, to fully utilize the resource regeneration function, not only can solve the problem of its possible pollution, but also replace the general man-made The raw materials consumed in the stone process. Therefore, it is necessary to develop a set of inventions that can solve the related environmental problems and the shortcomings of the prior art. [ SUMMARY OF THE INVENTION The main object of the present invention is to overcome the above problems encountered in the prior art and to provide for use. The refining and flotation ash produced by the waste I rumination process is used as a raw material to produce artificial stone complexes and materials with high added value at room temperature to achieve waste resource reuse. The secondary objective of the present invention is to provide a granule-reinforced material which is a granulated reinforcing material, and plays a mechanical strengthening role in the composite material, so as to promote the strength, hardness and resistance of the artificial money. method. ^ Another part of the invention - the purpose is to provide - the kind of refining scum and dust ash..., Weihua domain oxygen cutting, etc., to add fuel and anti-oxidation green. I material 枓 _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ To provide a way to reduce costs, 1 can use = regenerate Beiyuan' to further reduce the environmental benefits of consuming natural resources and destroying the environment, and promote the benefits of green materials and green construction to reproduce the benefits of color resources. 'a industry and green 201245102 . - .... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . The production process of Kanadai or the original artificial stone composite material, the raw material to be added is the method of materializing and recycling the product with aluminum scum and dust ash. The present invention is a refinery. The manufacturing method of the aluminum slag artificial stone composite material 'the smelting ash which is obtained after the waste aluminum regeneration raw material is regenerated by the waste aluminum smelting treatment, and the mixing is carried out with the resin in the range of 42.5~64. 'Adding hardener, defoamer and accelerator together The mixed slurry is further washed and cast into a molding die, and is subjected to cross-linking and solidification at a normal temperature to form a body, and the film is removed, thereby preparing an aluminum-smelting slag artificial stone composite material. [Embodiment] 凊 Refer to "Fig. 1 and Fig. 2" for the structure of the present invention and a schematic diagram of the manufacturing process of the present invention. As shown in the figure: the present invention is a can of red stone composite material. The manufacturing method ' is __ refining smelting process produced by the refining slag as raw materials, in order to achieve the purpose of recycling waste resources, to manufacture A with a high additional man-made; 5 composite view. The artificial stone composite 1 includes - The body's composition consists of refining _ slag ii, resin 1-2, jingbu agent 13, hardener i 4 and accelerator! 5, which will be used to add waste to the regenerative rejuvenation of the original age. The amount is between 42 5 ~ 64.0 wt% _ mixed with the resin, _ add hardener, defoaming money, swim into a mixed lining, county Weihe slanting silk in the molding mold 'waiting at its normal temperature After the joint is solidified into a handle, the film is released, that is, 201245102 is obtained - The type of artificial composite material which is hardened at room temperature and has a vertical length. The flow and the flow are as shown in Fig. 2, which includes at least the following steps: (4) Preparation step 2: Recycling waste aluminum recycling raw material, and the waste aluminum Then. Shengyuan _ waste _ smelting treatment, in the silk regeneration, produce green smelting furnace stains (hereinafter referred to as "smelting Shao furnace") including scum (Dr〇ss) and refining dust collection ash, the float in the basin The powder is sold, the coarse chopped chicks are recycled through the shovel; the fine granules are pulverized, ground and passed through a sifting treatment with the sifting ash, and the stalks are mixed with the ash. Powder, and then the slag/dust ash powder is subjected to powder_storage treatment for dry_storage; and (Β) reaction molding step 2 2: adding the above-mentioned refinery to dust ash powder plus = 33J~61.5 wt % of the resin and 〇~3 5 plus% of the defoamer after the ratio of the juice treatment, then add the W5 can hardener and the accelerator for the combined treatment to become the age-turned The paving treatment is carried out in the form of a preliminary treatment of the artificial stone composite material, and then placed in a normal temperature environment for the final fine temperature curing treatment. It is hardened to produce an artificial stone composite material, and after being separated from the film, a refining artificial stone composite material is obtained by cutting and trimming processing, stacking storage processing, grinding and polishing, and the like. It can be used as a finished product such as a reversible resin decorative board, a scale board, a laminated board, a movable partition wall and a resin board. The above steps are further enrolled by a vacuum-removing element casting, which is recorded in the presence of a mixed slurry. The above steps (A) waste Ming renewable raw materials are used for old waste materials, and can be used to hide Wei, car car miscellaneous gifts, _ silk Wei Pin Ming 201245102 • - . . . . -. · · · · - - - _ :. .- The above step (B) resin is unsaturated polyester resin' density is between U1~1 · 13 g/cm3; hardener is peroxide Methyl Ethyl
Ketone Peroxide,ΜΕΚΡΟ),屬於常溫硬化劑;以及促進劑係 為辛酸鈷(Cobalt Octoate) ’内含6 wt%鈷金屬,其為紫紅色 液體’用以促進聚合反應。 本發明針對煉鋁爐渣人造石複合材料之組成成份,如煉鋁 爐渣與不飽合聚酯樹脂,進行多組配比實驗,並藉由加入消泡 瓶導碌真级解域序,以改善人造錢錄料試體之 敏您程度。其整體架構如第1圖所示。當操作時,本發明係以 控制鋁爐渣混合比例及其它製程因子,進行一系列複合材料 餅’並㈣其基本雛,包含酿、吸轉、硬度、抗壓強 度及抗彎強度等;於-較佳實施例中,煉铭爐潰人造石複合材 料之配比’如下表-絲。本實酬之配比原縣使驗多之 煉罐潰,分職行添加量為44.4 Wt%、5〇.〇 wt%、53 3罐 、57Λ wt%及6L5赠%等5種試驗,藉以增加其再利用數量^ 檢測。 44.4 抽真空(分鐘) 500Ketone Peroxide, 常), is a room temperature hardener; and the accelerator is Cobalt Octoate, which contains 6 wt% cobalt metal, which is a purplish red liquid to promote polymerization. The invention aims at improving the composition components of the aluminum-smelting slag artificial stone composite material, such as aluminum slag slag and unsaturated polyester resin, and performing multi-group matching experiments, and improving the domain order by adding a defoaming bottle to improve the domain order The amount of artificial money recorded in the test is sensitive to your degree. The overall structure is shown in Figure 1. When operating, the present invention performs a series of composite cakes by controlling the mixing ratio of aluminum slag and other process factors, and (4) its basic chicks, including brewing, suction, hardness, compressive strength and flexural strength; In a preferred embodiment, the ratio of the smelting furnace to the artificial stone composite material is as follows: The ratio of the actual remuneration is the same as that of the original county. The amount of the sub-sector is 44.4 Wt%, 5〇.〇wt%, 53 3 cans, 57Λ wt% and 6L5%. Increase the number of reuses ^ detection. 44.4 Vacuum (minutes) 500
533_ _533_ 53.3 0.25 0.54 0.71 煉减_樹_ 消泡劑⑽) 400 400 400 3 400 350 4 400 5 400 6 400 350 7 400 350 8 400 350533_ _533_ 53.3 0.25 0.54 0.71 Refining _tree _ defoamer (10)) 400 400 400 3 400 350 4 400 5 400 6 400 350 7 400 350 8 400 350
S 201245102 9 400 350 53.3 0.89 10 400 350 53.3.. 1.25 11 400 350 53.3 3.43 益 12 400 350 53.3 0.54 15 請參閱『第3圖』所示,係本發明煉鋁爐渣添加量與混合 槳料黏度之關係示意圖。如圖所示:為固相含量對混合漿料黏 度之影響。在成型過程中,為了能夠具有良好之漿體流動性, 並順利於模具内成型’以達到較高之煉鋁爐渣再利用添加量, 因此’漿料中需以固相含量較高而黏度低者為佳。在分散性良 好之條件下’混合漿料黏度隨固相含量之增加而增大。當煉鋁 爐渣再利用添加量從44.4 wt%上升到53.3 wt%時,黏度急劇 上升,而固相添加量從53.3 wt%上升到61.5 wt%時,黏度則 緩慢上升。當固相添加量超過615wt%之漿料由於黏度過大, 漿體流動性不佳’已不適於進行澆鑄成型。因此本發明較佳之 煉銘爐渣再利用添加量係介於44.4〜61.5 wt%之間。 良好之煉鋁爐渣人造石複合材料物性,係以密度低、硬度 n及吸水率低者為較佳特性,本發明煉鋁爐渣人造石複合材料 即具備有此-般建材之基本物性,適合作為綠色建材使用。以 下將分別進行密度、硬度、吸轉、抗㈣度及抗彎強度試驗 .· • , · ,請參閱『第4圖及第5圖』所示’係分別為本發明煉叙爐 邊添加量與人造;5複合材料之密度隱*意目、及本發明消泡 劑添加量與人造石複合材料之密賴赫賴。如騎示:將 煉銘爐紅造石複合材料裁切為佩)χ 2()(w) χ 2()(τ)酿之 尺寸進行式如第4圖所示,隨著煉銘爐逢含量之增加 ,會增加試鮮赠叙質量,因此,人造石複合材料之密度 201245102 . - .. -- *· - ... . ..... .. .. . .、 ·. 呈現升高之趨勢,當煉鋁爐渣添加量為44.4〜61.5wt%時,入 :造石複合材料之密度介於之間。 ^為了增加人造石複合材料試體之緻密性,本發明在製作程 加人/肖摘鱗低漿料之黏度’進而減少試射之氣海。 ^第5圖所τ 隨華消泡劑添加量之增如,人造石複合材料之· 选度呈現升间之麟’當消泡劑添加量為〇〜〇 % Μ。,。時複 合材料之密度介於㈣〜⑽加3之間。然而,當消泡劑添 加量大於0.54wt/〇時’漿體黏度過低,反而容易起泡’使得成 型後之人造石複合材料試體密度降低。因此在製作程序中本 發明消泡劑之添加量將固定為〇54wt%,俾以製得較緻密之人 造石複合材料試體。 . . . · · • , 請參閲『第6圖及第7圖』所示,係分別為本發明煉鋁爐 渣添加量與人造石複合材料之吸水率關係示意圖、及本發明消 泡劑添加量與人造石複合材料之吸水率關係示意圖。如圖所示 :本實施例根據中國國家標準〇^9715,將人造石複合材料 試體裁切成長方體,大小為長度75 mm、寬度25胃及厚度3 mm之尺寸進行吸水率測試。本實施例係將試體於5〇〇c烘箱 中加熱處理24小時,再將之浸於去離子水中24小時,依據含 浸前與含浸後之重量變化來計算人造石複合材料試體之吸水 . . · 率。如第6圖及第7圖所示,人造石複合材料試體之吸水率與 • . . ,. 煉铭爐產及消泡劑之添加量,並未呈現線性之關係。在煉铭爐 • ·S 201245102 9 400 350 53.3 0.89 10 400 350 53.3.. 1.25 11 400 350 53.3 3.43 益12 400 350 53.3 0.54 15 Please refer to the figure “3” for the addition of aluminum slag and the viscosity of the mixed slag of the present invention. Diagram of the relationship. As shown in the figure: the effect of solid content on the viscosity of the mixed slurry. In the molding process, in order to be able to have good slurry fluidity and smoothly form in the mold to achieve a higher amount of aluminum slag reuse, the slurry needs to have a higher solid content and a lower viscosity. It is better. Under the condition of good dispersibility, the viscosity of the mixed slurry increases with the increase of the solid phase content. When the amount of aluminum slag reuse increased from 44.4 wt% to 53.3 wt%, the viscosity increased sharply, and when the solid phase addition increased from 53.3 wt% to 61.5 wt%, the viscosity increased slowly. When the slurry having a solid phase addition amount exceeding 615 wt% is too large in viscosity, the slurry fluidity is poor, which is not suitable for casting molding. Therefore, the preferred amount of refining slag reuse in the present invention is between 44.4 and 61.5 wt%. The physical properties of the good aluminum slag artificial stone composite material are characterized by low density, hardness n and low water absorption. The aluminum slag slag artificial stone composite material of the invention has the basic physical properties of the general building material, and is suitable as Use of green building materials. The following tests will be carried out for density, hardness, suction, resistance (four) and bending strength. · · · · Please refer to the "Figure 4 and Figure 5" for the addition of the refining furnace side of the present invention. And the artificial; 5 density of the composite material, and the amount of defoamer added by the invention and the artificial stone composite material. Such as riding: the smelting furnace red stone composite material is cut into χ) χ 2 () (w) χ 2 () (τ) brewing size as shown in Figure 4, with the refining furnace The increase in the content will increase the quality of the test-free gift. Therefore, the density of the artificial stone composite material 201245102 . - .. -- *· - ... . . . . . . . . . . . The high trend, when the amount of aluminum slag added is 44.4~61.5wt%, the density of the in-stone composite is between. In order to increase the compactness of the artificial stone composite sample, the present invention adds the viscosity of the low-slurry to the manuscript in the production process, thereby reducing the sea of test firing. ^ Figure 5 τ With the increase of the amount of antifoaming agent added, the selection of artificial stone composite material shows the rise of Lin's when the amount of defoamer added is 〇~〇 % Μ. ,. The density of the composite material is between (4) and (10) plus 3. However, when the amount of the antifoaming agent added is more than 0.54 wt/〇, the slurry viscosity is too low, and it is easy to foam, so that the density of the artificial stone composite sample after molding is lowered. Therefore, the amount of the antifoaming agent of the present invention to be added in the preparation process is fixed at 54 wt% to prepare a denser man-made composite sample. . . . · · · , Please refer to the "Figure 6 and Figure 7", which are respectively a schematic diagram showing the relationship between the amount of aluminum slag added and the water absorption of the artificial stone composite material of the present invention, and the addition of the defoaming agent of the present invention. Schematic diagram of the relationship between the amount and the water absorption of artificial stone composites. As shown in the figure: According to the Chinese national standard 〇^9715, the artificial stone composite sample body is cut into a rectangular shape, and the water absorption rate is tested by a size of 75 mm in length, 25 in width and 3 mm in thickness. In this embodiment, the test body is heat-treated in a 5 〇〇 oven for 24 hours, and then immersed in deionized water for 24 hours, and the water absorption of the artificial stone composite sample is calculated according to the change in weight before impregnation and after impregnation. · Rate. As shown in Fig. 6 and Fig. 7, the water absorption rate of the artificial stone composite sample does not exhibit a linear relationship with the addition amount of the refining furnace and the defoaming agent. In the furnace of refining •
渣介於44.4〜61.5 wt%與消泡劑介於〇〜3.43 wt%之添加量範 圍内’試體吸水率係分別介於0.8〜1.3%與0.8〜1.1〇/0。由於 吸水率小者較不易發生因滲水,與受到熱賬冷縮所導致之材料 表面龜裂、整塊建材剝落、材料機械強度變弱及使用安全性等S 201245102 • ..: · - , . · .., · .The slag is between 44.4 and 61.5 wt% and the defoaming agent is in the range of 〇~3.43 wt%. The water absorption of the sample is between 0.8 and 1.3% and 0.8 to 1.1 〇/0, respectively. Because of the small water absorption rate, it is less prone to water seepage, cracking of the surface of the material caused by shrinkage of the heat account, peeling of the whole building material, weakening of the mechanical strength of the material, and safety of use, etc. S 201245102 • ..: . · .., · .
1題依CNS 9715規疋鑄型板吸水率需小於〇.5%,_而cNS 11366熱固性树脂裝飾板則未規範此試驗項目,雖然本實施例 使用細t简製作之試體,獻於⑽9715規範標準· #仍可藉製作程序與配比設計來作調整,以符合⑽㈣之 規定。 . j · · · ,. - · 未請參閲『第8圖及第9圖』所示’係分別為本發明煉鋁爐 渣添加量與人造石複合材料之含水率關係示意圖、及本發明消 棚添加量與人拉複合㈣之含轉關細細。如圖所示 .將人造石複合材料裁切成長度75酿、寬度25醜及厚度3 麵之試體進行含水率測試。試體於室溫下靜置3天達到平衡 ^將試體放置於加熱裝置中加熱烘乾至怪重,再根據供乾前 f試體之重里變化’計算人造石複合材料試體之含水率◊如第 8圖及第9圖所示’兩相鄰長細,其中左側分別表示為煉銘 爐〉查及消泡劑添加量’右側則表示為人造石複合材料含水率。 由圖中可知,人造石複合材料試體之含水率與煉銘爐渣及消泡 劑添加量’並未呈現練性之關係。在煉铭爐渣介於444〜& 5 wt%與消鋪介於0〜3:43 wt%之添加量範圍内,試體含水率 係/7別〃於G.5〜1.8%與G.8〜丨1% ^雖然⑽9715鳞型板與 CNS 11366細性樹脂裝飾板未規範此試驗項目,惟建築用材 料之含水率同樣為顯示材料特性之參考指標,含水率,丨、者亦較 不易文到熱脹冷縮所導致材料表面龜裂、整塊建材剝落、材料 機械強度變弱及使用安全性等問題。 請參閱『第1 〇圖〜第1 3圖』所示.,係分別為本發明煉 銘驗添加量與人造石複合材料試體細之巴柯爾 (Barcol)1) According to CNS 9715, the water absorption rate of the cast plate should be less than 5%.5%, while the cNS 11366 thermosetting resin decorative board does not standardize this test item. Although this example uses the sample produced by the thin t simple, it is presented at (10) 9715. Normative Standards # # can still be adjusted by the production process and the proportioning design to meet the requirements of (10) (4). j · · · ,. - · Please refer to the "Figures 8 and 9" for the relationship between the amount of aluminum slag added and the moisture content of the artificial stone composite material of the present invention, and the present invention The amount of shed added and the compounding of the person (4) are fine. As shown in the figure, the artificial stone composite was cut into a length of 75, a width of 25 ug, and a thickness of 3 to test the moisture content. The test body is allowed to stand at room temperature for 3 days to reach equilibrium. The test piece is placed in a heating device to be heated and dried to a strange weight, and then the water content of the artificial stone composite sample is calculated according to the change in the weight of the sample before the drying. For example, in Figure 8 and Figure 9, the two adjacent lengths, where the left side is indicated as the refining furnace and the amount of defoaming agent added, the right side is expressed as the moisture content of the artificial stone composite. As can be seen from the figure, the moisture content of the artificial stone composite sample and the addition amount of the smelting furnace slag and the defoaming agent are not practicable. In the range of the addition amount of smelting slag between 444~& 5 wt% and hopping between 0~3:43 wt%, the test water content is /7 not to G.5~1.8% and G. 8~丨1% ^Although the (10)9715 scale board and CNS 11366 fine resin decorative board are not standardized for this test item, the moisture content of the building materials is also a reference indicator for the characteristics of the displayed materials. The moisture content is not easy. The problem is that the surface of the material is cracked, the whole building material is peeled off, the mechanical strength of the material is weakened, and the safety of use is caused by the thermal expansion and contraction. Please refer to the "Picture 1 to Figure 1 3". This is the barcol of the invention and the artificial stone composite material.
硬度關係示意圖、本發爾銘軸添加量與人造石複合材料試S 201245102 • · · . • ... " ., ........... , . '.. . • . 1 · . , · . - . - . . 體剖面^巴柯爾硬度關係示意圖、本發明消泡劑添加量與人造 石複合材料試體表面之巴柯爾硬度關係示意圖、及本發明消泡 劑添加量與人造石複合材料試體剖面之巴柯爾硬度關係示意 圖。如圖所示:本實施例板據ASTM D2583標準’將人造石 複合材料裁切成大小為50 8胃(D) x 3 2 _ (H)之圓盤尺寸 試體’進行人造石複合材料試體巴柯爾硬度測試。利用巴柯爾 硬度計’並引用ASTM D2583與町丨5測試硬質強化塑料 之壓痕硬度標準試驗方法,可測試煉鋁爐渣人造石複合材料之 硬度。如第1 0圖所示,人造石複合材料之硬度隨煉鋁爐渣含 量增加而增大’當含量超過50 wt%時,表面硬度值增加幅度 較;^,在煉銘爐渣添加量為61 5㈣時,硬度平均值為4〇乃 ’右與不飽和聚轉脂未添加填充料(煉銘爐渣)硬化後之硬 度35相比’貞I丨添加;對人造^複合材料之表面硬度係 明顯有助益。如圖所示,人造石複合材料試體剖面硬度 之增加趨勢與表面硬度係為一致,惟在同一練銘爐潰添加量之 情況下,人造石複合材料試體剖面硬度較試體表面硬度較高, 此係試體剖面單位體積之固體含量增加所致。 另外’本發明除了試驗煉叙爐渣添加量與人造石複合材料 賴硬度之_之外,_試添加消_對人造石複合材料試 體硬度影響。如第11圖及料2騎示,姻中可知,消泡. 娜加量之多寡,不會對人造石複合材料試體之硬度產生變化 ’但對試體之麵強度财日聰之影響(如後述第Η圖、 1 8圖所示)。 。.二 201245102 . . -...· ' . -. . - - . · _ • . . . · - -• · . . - ·. - CNS 9715規定鑄型板巴柯爾硬度需大於35,而CNS 11366熱 固性樹脂裝飾板則未規範此試驗項目觀々,且前建議使用煉銘 爐’/查配比所製作之人造石複合材料試體,係大於CNS 9715所 規範之數值’符合CNS 9715之規定。 請參閱『第14圖〜第16圖』所示’係分別為本發明煉 鋁爐渣添加量與人造石複合材料之抗壓強度關係示意圖、本發 明消泡劑添加量與人造石複合材料之抗壓強度關係示意周、及 本發明人造石複合材料抽真空脫泡後之抗壓強度與有無添加 消泡劑試體之比較示意圖。如圖所示:煉鋁爐渣人造石複合材 料抗壓強度之測試’依據測試標準ASTM Μ%,每一配比設 計測試試體數目為5個,試體大小為5 em (D) x 1G em (H)。如 第1 4圖所示,人造石複合材料試體隨著煉鋁爐渣添加量之增 加’其抗縫度有增蚊聰,在雜驗添加量為叫〜位 wt%下’其抗壓強度值介於74〜9〇廳之間。上述實驗結果 符合本發明⑽金屬雜產生之煉麟雜煉轉塵灰為顆 粒狀強化材料’在人造石複合材料中扮演機械性質之加強者, 可促進人造石複合材料之機械強度之設計原則— 第15圖顯示消泡劑之添加對試體之緻密程度有明顯之 改善;相對而言’也使得抗壓強度有_之提升。由圖中可見 ,當舰劑添加量介於〇〜〇.54㈣時,人造叾複合材料試體 隨著消泡劑添加量之增加,其抗壓強度亦有增加之趨勢,旅介 =77〜85 MPa之間。然而,若添加量超過〇 54糾%後,試體 抗壓強度則開始減弱,最後約為71 Mpa。 14 201245102 -· · · · · ·· · . · • · ·-. . .- .... ........ · - ^ . . ..' .., -.· . ' · 以上藉由消泡劑之添加,雖可使試體中氣泡存在之數量滅 少’惟改善情形仍有極限。因此,在製作過程中,乃導入抽真 空脫泡單元,以進一步去除漿體中存在之氣泡。 本發明以抽真空後人造石複合材料試體,其尺寸為30 X 3〇 X 3 cm ’與尺寸為10 x 10 x 6〇 cm之木级人造石複合材料試體 作比較。實驗結果如第丄6圖所示,顯示消泡劑之添加,再加 • · . 上抽真空脫泡單元之協助’試體外觀與内部剖面皆呈現相當緻 猞’孔洞已幾乎不存在’相對地,也使得抗壓強度有明顯之提 升,因此,人造石複合材料試體隨著消泡劑之添加與抽真空脫 泡,係可使抗壓強度有增加之趨勢,其抗壓強度可提高而達 101 MPa。雖然CNS 9715鑄型板與CNS 11366熱固性樹脂襄 飾板未規範此試驗項目,惟商業化產品,如美俐家御石,其試 體抗壓強度測試值為840 kg分cm2 (約84.7碰&),本發明所 創作之人造石複合材料之抗壓強度,明顯優於市面上之產品, _具有競爭力。. 請參閱『第1 7圖友第1 8圖』所示,係分別為本發明煉 雜潰添加量與人造石複合材料之抗弯強度關係示意圖、及本 發㈣輔添加量與人造石複合材料之抗㈣度關係示意圖 。㈣所示:煉銘爐渣人造石複合材料抗彎強度之測試,依據 測試標準ASTM D790,每-配比設計測試試體數目為5個, 試體大小為l5〇(L) X 38(W) χ 9(τ)咖之長方型尺寸。如第工 7圖所示,人造石複合材料試體隨著煉鋁爐渣添加量之增加, 其抗彎.強度有增加之趨勢,在煉祕轉加量為44〜53祕 下’其抗彎做值介於4〜5 kgf/mm2之間;然而當煉祕 逢添加量大於53 wt%時,抗彎強度_始變弱,在煉銘爐渣s 15 201245102 - . . . ^ ’ --添加量為57與62 wt%時,人造石複合材料試體抗彎強度值分 別為4.8與41^伽血2。由前述實施例第11圖及第12圖之 煉鉉爐渣添加量與人造石複合材料之巴柯爾硬度關係所示,可 去後#又曲線斜率大於前段,因此,人造石複合材料抗彎強度之 減弱可能係因為:當煉鋁爐渣添加量大於53糾%時,人造石 複合材料試體特性變得更硬且脆,由於硬而脆之材料具有高彈 性模數’小之伸長率’因此可能在破壞以前就發生降服現象。 故,煉鋁爐渣添加量小於53別%之人造石複合材料係屬於 硬而軔之材料,具有高彈性模數與高應力,可增加材料強度測 試時之應變,使得斷裂強度發生在降服強度之後,因此使得人 造石複合材料試體之抗彎強度測試值增加。 如第18圖所示,消泡劑之添加對試體之緻密程度有明顯 地改善’相對而言,也使得抗彎強度有明顯地提升。由圖中可 知,當消泡劑添加量為0〜0.89加%時,其抗彎強度值介於4 9 〜5.9 kg分mm2之間,顯示人造石複合材料試體之抗彎強度係 隨著消泡劑添加量之增加而有增加之趨勢^然而,當添加量超 過0.89 wt%後’試體抗彎強度則開始減弱,其最後抗彎強度值 約為4.8 kgfton^若由增加抗彎強度之觀點來決定消泡劑最 佳添加星,則消泡劑添加量在〇 89將得本發明之選擇;然 練據前述試體抗顧度所_選出之最佳消細添加量(〇54 wt%)係撕差異,gj此,本拥分簡由比雛彎強度、抗 壓強度之增加比例與經濟成本,選擇消泡劑添加量〇54祕 為本發明之最佳添加量◊雖然CNS97U鑄型板(如普通、次 級垂直板與襯裡板)與CNS 11366 _性樹脂裝飾板未規範 此試驗項目,比較台灣已商業化產品,如美倒家御石,其抗壓s 16 201245102 - . . . .:. ' 強度為84 MPa ’抗彎強度為4.6 kgf/mm2,品本發明所創作之 人造石複合材料之抗壓強度為85·5 MPa,抗彎強度為5.0 kgf/mm2 ’與市面上之產品相當,具有競爭力。 此外’本發明尚對煉鋁爐渣人造石複合材料之毒性特性溶 出(TCLP )作試驗。在TCLP試驗中分析重金屬項自,包括 硒、汞、鉛、鎘、鉻(總鉻)、六價鉻、鋇及砷等有毒重金屬 。其中’煉鋁爐渣人造石複合材料卩只值及溶出之重金屬濃度 如下表二所示,PH值為6.16,可見毒性溶出重金屬濃度遠低 於法規標準值。因此’以煉鋁爐渣為原料之人造石複合材料試 體’經由TCLP之測試後並無重金屬溶出之疑慮,可以取代原 製程之原料天然石粉,如此,則能減少天然資源之耗用,避免 原料開採對環境造成衝擊。 表二Schematic diagram of hardness relationship, Benfair Ming axis addition amount and artificial stone composite material test S 201245102 • · · . • ... " ., ........... , . '.. . 1 · . , · · - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Schematic diagram of the relationship between the amount of addition and the Barcol hardness of the cross section of the artificial stone composite. As shown in the figure: the plate of this embodiment is cut according to the ASTM D2583 standard 'the artificial stone composite material into a disk size test piece of size 50 8 stomach (D) x 3 2 _ (H) for artificial stone composite material test Body Bachel hardness test. The hardness of the aluminum-smelting slag artificial stone composite can be tested by using a Bakr hardness tester and citing the ASTM D2583 and 丨5 test hard-hardening plastics for the indentation hardness standard test method. As shown in Figure 10, the hardness of the artificial stone composite increases with the increase of the content of the aluminum slag. 'When the content exceeds 50 wt%, the surface hardness value increases by a larger amount; ^, the amount of the slag added in the slag is 61 5 (four) When the hardness average value is 4〇, the hardness of the right and unsaturated polycondensed grease without adding filler (refinement slag) is 35 compared with '贞I丨; the surface hardness of the artificial composite is obviously Help. As shown in the figure, the increase in the hardness of the cross-section of the artificial stone composite is consistent with the surface hardness. However, in the case of the same amount of the furnace, the cross-section hardness of the artificial stone composite is higher than that of the test surface. High, the solid content of the unit volume of this test body is increased. In addition, the present invention has the effect of testing the hardness of the artificial stone composite sample in addition to the amount of the slag slag added and the hardness of the artificial stone composite. As shown in Figure 11 and material 2, it is known in the marriage that defoaming. The amount of Na added does not change the hardness of the artificial stone composite test piece, but the effect on the surface strength of the test piece is As shown in the figure below, Figure 18 shows). . .2012.102102 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . CNS 11366 thermosetting resin decorative board does not standardize this test project, and it is recommended to use the artificial stone composite material produced by the smelting furnace '/check ratio, which is greater than the value specified by CNS 9715' in accordance with CNS 9715. Provisions. Please refer to the figure "Fig. 14 to Figure 16" as a schematic diagram showing the relationship between the amount of aluminum slag added and the compressive strength of the artificial stone composite material, the amount of the defoaming agent added in the present invention and the resistance of the artificial stone composite material. The relationship between the compressive strength and the comparison between the compressive strength after vacuum defoaming of the artificial stone composite of the present invention and the presence or absence of the added defoaming agent are shown. As shown in the figure: The test of compressive strength of aluminum slag artificial stone composite material is based on the test standard ASTM Μ%. The number of test samples for each ratio design is 5, and the sample size is 5 em (D) x 1G em. (H). As shown in Figure 14, the artificial stone composite material with the increase in the amount of aluminum slag added, its anti-seam degree has increased Mosquito, the amount of addition in the miscellaneous test is called ~ bit wt% 'the compressive strength The value is between 74~9〇. The above experimental results are in accordance with the invention (10) The metal-mixed smelting ash-to-dust granule-reinforced granules are a reinforcing material of the mechanical properties of the artificial stone composite material, and can promote the design principle of the mechanical strength of the artificial stone composite material - Figure 15 shows that the addition of the defoamer has a significant improvement in the densification of the test piece; relatively speaking, 'there is also an increase in the compressive strength. It can be seen from the figure that when the addition amount of the agent is between 〇~〇.54(4), the compressive strength of the artificial enamel composite test material increases with the increase of the amount of defoaming agent. Traveling = 77~ Between 85 MPa. However, if the amount added exceeds 〇 54%, the compressive strength of the test piece begins to decrease, and finally it is about 71 Mpa. 14 201245102 -········ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . The above is added by the defoaming agent, although the amount of bubbles present in the test body can be reduced. However, there is still a limit to improvement. Therefore, during the production process, a vacuum degassing unit is introduced to further remove the bubbles present in the slurry. The present invention compares the artificial stone composite material after vacuuming, having a size of 30 X 3 〇 X 3 cm ' with a wood-scale artificial stone composite sample having a size of 10 x 10 x 6 〇 cm. The experimental results are shown in Figure 6, showing the addition of antifoaming agent, plus • · · The assistance of the upper vacuum defoaming unit's appearance and internal profile are quite convincing 'the hole is almost non-existent' relative The ground also makes the compressive strength significantly improved. Therefore, the artificial stone composite material with the addition of defoaming agent and vacuum defoaming can increase the compressive strength and increase the compressive strength. And up to 101 MPa. Although CNS 9715 mold plate and CNS 11366 thermosetting resin enamel trim board are not standardized in this test project, commercial products such as Meijiajia Yushi have a test value of 840 kg min cm2 (about 84.7 hit &;), the compressive strength of the artificial stone composite material created by the invention is obviously superior to the products on the market, and _ is competitive. Please refer to the "Picture of Figure 1 7th Figure 8", which is a schematic diagram showing the relationship between the amount of blending and mixing of the present invention and the flexural strength of the artificial stone composite material, and the compounding amount of the artificial hair (4). Schematic diagram of the resistance of the material to the (four) degree. (4) As shown in the test: The bending strength test of the slag slag artificial stone composite material, according to the test standard ASTM D790, the number of test pieces per design ratio is 5, the sample size is l5 〇 (L) X 38 (W) χ 9 (τ) coffee rectangular size. As shown in Figure 7, the artificial stone composite material with the increase in the amount of aluminum slag added, its bending strength has an increasing trend, in the refining secret of the amount of 44~53 secrets under its 'bending resistance The value is between 4~5 kgf/mm2; however, when the addition amount is more than 53 wt%, the bending strength _ begins to weaken, and it is added in the smelting slag s 15 201245102 - . . . ^ ' -- When the amount is 57 and 62 wt%, the flexural strength values of the artificial stone composite specimens are 4.8 and 41 gamma blood, respectively. According to the relationship between the amount of the slag slag added in the eleventh and twelfth embodiments of the foregoing embodiment and the Bakker hardness of the artificial stone composite material, the slope of the curve can be changed to be larger than the anterior segment, and therefore, the flexural strength of the artificial stone composite material is obtained. The weakening may be due to the fact that when the amount of aluminum slag added is more than 53%, the properties of the artificial stone composite become harder and brittle, since the hard and brittle material has a high elastic modulus 'small elongation'. Probability may occur before the damage. Therefore, the artificial stone composite material with less than 53% of the aluminum slag addition is a hard and sturdy material with high elastic modulus and high stress, which can increase the strain during the material strength test, so that the fracture strength occurs after the drop strength. Therefore, the test value of the flexural strength of the artificial stone composite sample is increased. As shown in Fig. 18, the addition of the defoaming agent significantly improved the density of the test piece. In contrast, the bending strength was also significantly improved. It can be seen from the figure that when the defoaming agent is added in an amount of 0 to 0.89%, the flexural strength value is between 4 9 and 5.9 kg min 2 , which indicates that the flexural strength of the artificial stone composite specimen is There is an increasing trend of the addition of defoamer. However, when the added amount exceeds 0.89 wt%, the flexural strength of the test body begins to weaken, and the final flexural strength value is about 4.8 kgfton^if the bending strength is increased. From the viewpoint of determining the best addition star of the defoaming agent, the addition amount of the defoaming agent in the 〇89 will be the choice of the present invention; however, the optimum amount of the fine addition added according to the above-mentioned test object resistance (〇54) Wt%) is the difference between the tears, gj, the percentage of the support is simplified by the ratio of the strength of the bending strength, the strength of the compressive strength and the economic cost. The amount of defoaming agent added is the best addition amount of the invention, although CNS97U casts Models (such as ordinary, secondary vertical and lining panels) and CNS 11366 _ resin decorative panels are not standardized for this test project, comparing Taiwan's commercial products, such as the United States, the pressure resistance s 16 201245102 - . . . .:. 'Strength is 84 MPa' and the bending strength is 4.6 kgf/mm2. Compressive strength as the artificial stone of the composite is 85 · 5 MPa, a bending strength of 5.0 kgf / mm2 'market and the products of comparable competitive. Further, the present invention is also tested on the toxic characteristic dissolution (TCLP) of an aluminum slag slag artificial stone composite. Heavy metals were analyzed in the TCLP test, including toxic heavy metals such as selenium, mercury, lead, cadmium, chromium (total chromium), hexavalent chromium, antimony and arsenic. The concentration of heavy metal in the aluminum slag composite stone composite and the dissolved heavy metal concentration are shown in Table 2 below. The PH value is 6.16. It can be seen that the concentration of toxic dissolved heavy metals is much lower than the regulatory standard value. Therefore, the 'artificial stone composite sample with aluminum slag as raw material' has no doubt about heavy metal dissolution after testing by TCLP, which can replace the natural stone powder of the original process, thus reducing the consumption of natural resources and avoiding raw materials. Mining has an impact on the environment. Table II
檢驗項目 檢驗值 方法偵測極限(MDL) 法規標準 單位c 氫離子濃度指數 6.16 ' 萃取液中六價鉻 ΝΕ)“ 0.0065 2.5 me/L 萃取液中總汞 ND 0.000037 0.2 me/T 萃取液中總砷 ND 0.0078 5 mcr/T 萃取液中總銅 ND --· 0.0062 15 ----- me/L 萃取液中總鉻 0.032 0.0061 5 me/T 萃取液中總鎘 ND 0.0059 1 rncv/T 萃取液中總鉛 ND 0.0065 5 me/T 萃取液牛總硒 ND 0.0085 1 萃取液中總鋇 ND 0.0060 100 — mg/L 其中’上表a表示檢驗值低於方法偵測極限之測定以NB表 不’亚註明其方法偵測極限值(MDL)及單位;b表示檢驗項 201245102 * · 二萃取液六祕稀釋1()倍後驗證之回收率符合方法管制範圍 ^檢驗值為10倍稀釋液之量離;e表示氫離子濃度指 為夏測時溶液體積與溫度。 _由上述各實射知,本發明人造錢合#料之試驗結_ 不’根據人造石複合材㈣雜度與工舰, 53 3 ^/〇> 石複合材狀紐與吸轉分職W g/^與 Μ% ;人造 石複合材料試體巴柯_硬度平均為37;缝缝與抗彎強^ 分別可達IGlMPa與5kg£W ;人造石複合概_耐化$ 腐蝕性與TCXP測微,人虹複合㈣物無·變化,春 性溶出重金屬濃度遠低於法規標準值。依據目前之試驗社果與 中國國家產品鮮,本發明之複合材料產品可^義為:^ 樹脂裝飾板(CNS 11366)、鑄型板(CNS 9715)及活^隔牆 (CNS 8072 )〇 回 本發明雜舰再_频化為人造石複合材料之邊際 效益,包括減少煉__埋處理對環境所造成之衝擊與負^ 。煉銘爐祕_所衍生之前化產品,可以增加再_廠^ 之營運收入’減少因掩埋處理所需付出之處置費用(16〇〇〜 2800元/嘴)。在原物料不斷漲價之時代,練峨潰資源再利用 ,可以取代或減少原來人造石複合材料生產過程,所需添加之 原物料,如氧化鋁、氫氣化鋁與氧化矽等。因此,煉銘爐渣之 材料化不失為一種降低成本之方法,且又能利用這些再生資源 ’進一步減少消耗自然資源與破壞環境,為具有相當大之環境 效盈之方法者。Test item test value method detection limit (MDL) regulatory standard unit c hydrogen ion concentration index 6.16 'hexavalent chrome in extract ΝΕ) " 0.0065 2.5 me / L total mercury in extract ND 0.000037 0.2 me / T total extract Arsenic ND 0.0078 5 mcr/T Total copper in the extract ND --· 0.0062 15 ----- me/L Total chromium in the extract 0.032 0.0061 5 me/T Total cadmium in the extract ND 0.0059 1 rncv/T Extract Total lead ND 0.0065 5 me/T Extract total selenium ND 0.0085 1 Total 钡ND 0.0060 100 — mg/L in the extract. 'The above table a indicates that the test value is lower than the method detection limit. Indicates the method detection limit value (MDL) and unit; b indicates the test item 201245102 * · The two extracts are diluted 1 () times and the recovery rate is verified according to the method control range ^ the test value is 10 times the amount of the diluent E; the hydrogen ion concentration refers to the solution volume and temperature during the summer test. _ From the above-mentioned actual shots, the experimental knot of the artificial money of the present invention _ not 'according to the artificial stone composite (four) heterogeneity and the ship, 53 3 ^/〇> Stone composites New and Absorbed W g/^ and Μ%; artificial stone complex The material test body Bacco _ hardness average is 37; seam and bending strength ^ can reach IGlMPa and 5kg£W respectively; artificial stone composite _ 耐化 $ Corrosive and TCXP micro, human rainbow composite (four) no change The concentration of heavy metals in spring dissolution is far lower than the standard value of the regulations. According to the current test results and the national products of China, the composite products of the present invention can be: ^ resin decorative board (CNS 11366), cast board (CNS) 9715) and the live partition wall (CNS 8072) to return the marginal benefits of the invention of the miscellaneous ship to the artificial stone composite material, including reducing the impact on the environment caused by the refining __ burial treatment. Secret _ derived from the previous product, can increase the operating income of _ factory ^ 'reduced the disposal costs for the burial treatment (16 〇〇 ~ 2800 yuan / mouth). In the era of rising prices of raw materials, training Reuse of resources can replace or reduce the original artificial stone composite production process, the raw materials to be added, such as alumina, aluminum hydride and ruthenium oxide. Therefore, the materialization of smelting slag is a way to reduce costs. And can use these regenerations Resources' further reduce the consumption of natural resources and environmental damage, and are the means to have considerable environmental benefits.
S 18 201245102 ' - - - · · 由此可知’本發明以舊廢鋁料為其熔煉資源再生之原料, 針對廢鋁再生冶煉產生之煉鋁浮渣與集塵灰等廢棄物利用已 建立之材料化技術’將之製作成複合材料資源化產品,並實驗 此類人造石複合材料之基本物理化學性質。由上述試驗可1, 該人造石複合材料乃兩種以上性質互補,且會產生加成性質並 具有更佳特性之材料。本發明以煉鋁浮渣與集塵灰為顆粒狀強 化材料’在人造石複合材料中扮演機械性質之加強者,促進人 造石複合材料之機械強度、硬度及耐磨性。另一方面由於練 料渣與集歡之主要化學成份,為無魏化轉氧化梦,、具 #耐高溫與耐燃之特性’以此特性為基礎,藉以增加複合材& 之=燃與抗氧化性。因此’本發佩煉料潰及集塵灰材料化 與資源化產品之創新,不僅創造廢棄物資源再利用之價值同 時,也完成實賊之廢棄崎贼理I作,可提高產品附加價 值’增加營運收入’並避免掩埋而對環境造成衝擊。另外,藉 此也可推動綠色材料、綠色營S、綠色產業及綠色資源再生利 用之益處。 ' ..... ·. - 綜上所述’本發明係一種煉鋁爐渣人造石複合材料之製造 方法可有效改善習用之種種缺點,係以煉銘爐渣為原料再 利用材料化為複合材料產品,可提高其附加價值,增加廠商資 源化產品收入’並減少掩埋費用之支出,延長掩埋場使用年 限’以避免對環境造成衝擊,並解決相關之環境問題,進而使 本發明之赶能更進步、更實用、更符合使用者之聊,確已 符合發明專利申請之要件,爰依法提出專利申請。 ,以上所述者,僅為本發明之較佳實施例而已,當不能以 此限疋本發明實施之範圍;故,凡依本發明申請專利範圍及發s 19 201245102 . ·' ' '. • · ; . · - · - · · · . :明說明書内容所作之簡單的等效變化與修飾,皆應仍屬明 專利涵蓋之範圍内。 • ·. . · · • . - · . -· ·. . · · - 【圖式簡單說明】 第1圖’係本發明之架構示意圖。 .第2圖,係本發明之製作流程示意圖。 Μ圖’烏發晴_絲加4無合漿_度之關係 示意圖。 _ · · · · 14« ’解發鴨織齡加量與人缸複合材料之麥 度關係示意圖。 第5圖,係本發明消泡劑添加量與人造石複合材料之密度 關係示意圖。 第δ圖,係本發明煉鋁爐渣添加量與人造石複合材料之吸 水率關係示意圖。 .. · . · 第7圖,係本發明消泡劑添加量與人造石複合材料孓吸水 率關係示意圖。+ .. 第8圖,係本發明煉鋁爐渣添加量與人造石複合材料之含 水率關係示意圖。 第9圖’係本發明消泡劑添加量與人造石複合材料之含水 率關係示意圖。 第10圖,係本發明煉鋁爐渣添加量與人造石複合材料試 體表面之巴柯爾硬度關係示意圖。 第11圖,係本發明煉鋁爐渣添加量與人造石複合材料試 體剖面之巴柯爾硬度關係示意圖。 第2圖,係本發明诮泡劑添加量與人造石複合材料試體 • · · · . 20 201245102 . ' · • . -· - - . 表®之巴柯爾硬度關係示意圖。.:S 18 201245102 ' - - - · · It can be seen that 'the invention uses the old waste aluminum material as the raw material for the refining of the smelting resources, and has established the waste utilization of the aluminum scum and the dust ash generated by the scrap aluminum refining and smelting. Materialization technology 'made it into a composite material resource product and tested the basic physicochemical properties of such artificial stone composite material. According to the above test, the artificial stone composite material is a material which is complementary to two or more kinds of properties and which has an addition property and a better property. The invention uses the aluminum scum and the dust collecting ash as the granular strengthening material' to strengthen the mechanical properties in the artificial stone composite material, and promotes the mechanical strength, hardness and wear resistance of the artificial stone composite material. On the other hand, due to the main chemical composition of the slag and Jihuan, it is a non-weihua oxidative dream, and has the characteristics of high temperature and flame resistance, so as to increase the composite material & Oxidizing properties. Therefore, 'the innovation of this product and the materialization of the dust and ash material and the innovation of the resource-based products not only create the value of recycling the waste resources, but also complete the thief's disposal of the thief, which can increase the added value of the product' Increase operating income' and avoid burial and impact on the environment. In addition, the benefits of green materials, green camp S, green industries and green resources recycling can be promoted. ' ..... ·. - In summary, the invention is a method for manufacturing an aluminum-smelting slag artificial stone composite material, which can effectively improve various disadvantages of the conventional use, and uses the refining slag as a raw material to re-use the material into a composite material. Products can increase their added value, increase the revenue of manufacturers' resource-based products and reduce the cost of landfill fees, extend the life of the landfills to avoid environmental impacts, and solve related environmental problems, thereby making the invention more efficient. Progress, more practical, and more in line with the user's chat, it has indeed met the requirements of the invention patent application, and filed a patent application according to law. The above is only the preferred embodiment of the present invention, and should not be limited to the scope of the present invention; therefore, the scope of the patent application and the s 19 201245102. · ' ' '. · · · · · · · · . : The simple equivalent changes and modifications made in the contents of the manual shall remain within the scope of the patent. • ····· • • - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Fig. 2 is a schematic view showing the production process of the present invention. Μ图 '乌发晴_丝加4无合浆_degree relationship diagram. _ · · · · 14« ′ Schematic diagram of the relationship between the amount of duck aging and the wheat composite. Fig. 5 is a schematic view showing the relationship between the amount of the antifoaming agent added in the present invention and the density of the artificial stone composite material. The δth diagram is a schematic diagram showing the relationship between the amount of aluminum slag added and the water absorption rate of the artificial stone composite material of the present invention. Fig. 7 is a schematic diagram showing the relationship between the amount of defoaming agent added in the present invention and the water absorption rate of the artificial stone composite material. Fig. 8 is a schematic view showing the relationship between the amount of aluminum slag added and the water content of the artificial stone composite material of the present invention. Fig. 9 is a schematic view showing the relationship between the amount of the antifoaming agent of the present invention and the water content of the artificial stone composite material. Fig. 10 is a view showing the relationship between the amount of the aluminum slag added in the present invention and the Bakr hardness of the surface of the artificial stone composite sample. Fig. 11 is a view showing the relationship between the amount of aluminum slag added in the present invention and the Barcol hardness of the artificial stone composite sample section. Fig. 2 is a diagram showing the relationship between the amount of the foaming agent added to the artificial stone composite material of the present invention and the artificial stone composite material. 2. 2012 · 2012. .:
第1請’縣發㈣細⑹量與人紅私材科體 剖面之巴柯爾硬度關係示意圖。V 胃1 4圖’ #本發明煉IS爐逢添加量與人造石複合材料之 抗壓強度關係示意圖' 第15圖,係本發明消泡劑添加量與人造石複合材料之抗 壓強度關係示意圖。 几 第16圖,係本發明人造石複合材料抽真空脱泡後之抗壓 強度與有無添加消泡劑試體之比較示意圖。 . · · · 第17圖’係本發明煉鋁爐渣添加量與人造石複合材料之 抗彎強度關係示意圖。 第18圖’係本發明消泡劑添加量與人造石複合材料之抗 彎強度關係示意圖。 【主要元件符號說明】 人造石複合材料1 煉鋁爐渣11 樹脂1 2 消泡劑13 硬化劑14 促進劑1 5 步驟(A)製備步驟21 步驟(B)反應成型步驟2 2 21The first is the relationship between the county (four) fine (6) volume and the human red private material body profile of the Barker hardness relationship. V 胃1 4图' # Schematic diagram of the relationship between the amount of the addition of the IS furnace and the compressive strength of the artificial stone composite material. Figure 15 is a schematic diagram showing the relationship between the amount of the defoaming agent added and the compressive strength of the artificial stone composite material of the present invention. . Fig. 16 is a schematic view showing the comparison between the compressive strength of the artificial stone composite material of the present invention after vacuum defoaming and the presence or absence of the added defoaming agent. Fig. 17 is a schematic view showing the relationship between the amount of addition of the aluminum slag of the present invention and the flexural strength of the artificial stone composite. Fig. 18 is a schematic view showing the relationship between the amount of the antifoaming agent of the present invention and the flexural strength of the artificial stone composite. [Explanation of main component symbols] Artificial stone composite material 1 Aluminum smelting slag 11 Resin 1 2 Defoaming agent 13 Hardener 14 Accelerator 1 5 Step (A) Preparation step 21 Step (B) Reaction molding step 2 2 21
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW100116924A TW201245102A (en) | 2011-05-13 | 2011-05-13 | Method of fabricating aluminum-dross imitation stone composite |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW100116924A TW201245102A (en) | 2011-05-13 | 2011-05-13 | Method of fabricating aluminum-dross imitation stone composite |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW201245102A true TW201245102A (en) | 2012-11-16 |
Family
ID=48094237
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW100116924A TW201245102A (en) | 2011-05-13 | 2011-05-13 | Method of fabricating aluminum-dross imitation stone composite |
Country Status (1)
| Country | Link |
|---|---|
| TW (1) | TW201245102A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI740141B (en) * | 2019-05-09 | 2021-09-21 | 中國鋼鐵股份有限公司 | Man-made building materials |
-
2011
- 2011-05-13 TW TW100116924A patent/TW201245102A/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI740141B (en) * | 2019-05-09 | 2021-09-21 | 中國鋼鐵股份有限公司 | Man-made building materials |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR102313251B1 (en) | Thermoset ceramic compositions and a method of preparation therefor | |
| CN101219902A (en) | Environment-protection dry type vibrating material and production method thereof | |
| RU2170716C1 (en) | Sand-polymer material | |
| CN113072314A (en) | Treatment method of household garbage incineration fly ash | |
| CN103771894B (en) | A kind of aerated bricks with antifreeze function and preparation method thereof | |
| CN119263700B (en) | Quick early-strength high-performance asphalt cold patch material at normal temperature and preparation method thereof | |
| CN100404239C (en) | A method of making glass fiber reinforced plastic products by using non-metallic powder of waste circuit boards | |
| CN109332576A (en) | A kind of casting high silicon precoated sand of high temperature resistant and preparation method thereof | |
| TW201245102A (en) | Method of fabricating aluminum-dross imitation stone composite | |
| US20080006383A1 (en) | Pulp Sludge Ash Composition for Producing Building Materials | |
| JP5587794B2 (en) | Composition containing specific metallocene and use thereof | |
| CN105271985A (en) | Special mortar for antibiotic and environmentally-friendly aerated bricks | |
| JP2017100888A (en) | Decorative flat plate and manufacturing method therefor | |
| CN114956794B (en) | Erosion-resistant rock wool furnace lining material and preparation method thereof | |
| CN107473710A (en) | A kind of electroplating sludge that blends prepares the method that clay brick process improves heavy metals immobilization effect | |
| CN110092610A (en) | The method for preparing artificial stone using the high alumina salt slurry that aluminium foil corrosion is formed | |
| CN105236899B (en) | A kind of electrolytic zinc acid leaching slag recycling innoxious use method | |
| CN109851279B (en) | A kind of artificial stone and preparation method thereof | |
| CN102505058B (en) | Metallurgical slag ladle bottom protecting material as well as preparation method and spray repairing method thereof | |
| JP2013513540A (en) | Manufacturing method of lightweight construction materials using asbestos waste | |
| CN102285782A (en) | Artificial jade based on building rubbish and manufacturing method thereof | |
| CN117383901A (en) | A kind of uranium tailings solidifying agent and solidifying method thereof | |
| CN108947239A (en) | A kind of preparation method of mobile phone tempered glass film | |
| CN109825195A (en) | A kind of preparation method being easily coated with vapor-permeable type lost foam paint | |
| CN104291745B (en) | A kind of method utilizing waste acid slag to prepare geo-polymer |