CN105503193A - 一种利用蓝晶石选矿尾矿转型转相制备Sialon/Si3N4-SiC复相耐高温材料的制备方法 - Google Patents
一种利用蓝晶石选矿尾矿转型转相制备Sialon/Si3N4-SiC复相耐高温材料的制备方法 Download PDFInfo
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- 239000000463 material Substances 0.000 title claims abstract description 45
- INJRKJPEYSAMPD-UHFFFAOYSA-N aluminum;silicic acid;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O INJRKJPEYSAMPD-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 229910052850 kyanite Inorganic materials 0.000 title claims abstract description 28
- 239000010443 kyanite Substances 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- 230000009466 transformation Effects 0.000 title abstract 4
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 75
- 239000000843 powder Substances 0.000 claims abstract description 69
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000002994 raw material Substances 0.000 claims abstract description 28
- 238000000034 method Methods 0.000 claims abstract description 24
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 18
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 11
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- 238000002156 mixing Methods 0.000 claims abstract description 7
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- 238000005516 engineering process Methods 0.000 claims abstract description 5
- 229910052581 Si3N4 Inorganic materials 0.000 claims abstract description 4
- 239000000919 ceramic Substances 0.000 claims abstract description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 20
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 11
- 238000005245 sintering Methods 0.000 claims description 11
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- 239000002699 waste material Substances 0.000 claims description 7
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- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 239000005864 Sulphur Substances 0.000 claims description 5
- 230000001681 protective effect Effects 0.000 claims description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 4
- 239000003245 coal Substances 0.000 claims description 4
- 230000006835 compression Effects 0.000 claims description 4
- 238000007906 compression Methods 0.000 claims description 4
- 230000035484 reaction time Effects 0.000 claims description 4
- 229910052786 argon Inorganic materials 0.000 claims description 2
- 239000006229 carbon black Substances 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000007789 gas Substances 0.000 claims description 2
- 238000005121 nitriding Methods 0.000 claims description 2
- 238000007493 shaping process Methods 0.000 claims description 2
- 238000002791 soaking Methods 0.000 claims description 2
- 229910000831 Steel Inorganic materials 0.000 abstract description 3
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- 239000010959 steel Substances 0.000 abstract description 3
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 abstract description 2
- 206010009691 Clubbing Diseases 0.000 abstract 1
- 238000005265 energy consumption Methods 0.000 abstract 1
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- 229910052710 silicon Inorganic materials 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- 239000002910 solid waste Substances 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
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- 239000003963 antioxidant agent Substances 0.000 description 1
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- 239000004566 building material Substances 0.000 description 1
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Abstract
本发明涉及一种利用蓝晶石选矿尾矿转型转相制备Sialon/Si3N4-SiC复相耐高温材料的方法,属于耐火材料制备技术领域。其特征是采用以蓝晶石选矿尾矿、碳质材料和高纯氮气为主要原料,经配料、球磨混料、高温碳热氮化还原反应以及除碳等工艺制备得到一种纯度较高的片状或棒状Sialon-SiC复相粉体;采用碳热还原氮化制得的Sialon-SiC复相粉体、氮化硅粉体和碳化硅粉体为主要原料,经配料、球磨混料后在非氧化气氛下烧结得到Sialon/Si3N4-SiC复相耐高温材料。采用蓝晶石选矿尾矿转型转相制备得到的Sialon/Si3N4-SiC复相材料具有良好的抗折强度与抗压强度,该工艺具有较高的转化率,可用于耐高温材料、陶瓷部件以及钢铁行业等。本发明所涉及的原材料成本及能耗低,蓝晶石选矿尾矿利用率高,不仅为蓝晶石选矿尾矿的利用开辟了新的途径,而且也减轻了对环境的污染,具有深远的环保意义和经济价值。
Description
技术领域:
本发明涉及一种利用蓝晶石选矿尾矿转型转相制备Sialon/Si3N4-SiC复相耐高温材料的制备方法,属于耐火材料制备技术领域。
背景技术:
蓝晶石选矿尾矿是蓝晶石矿开采过程中排放的工业废弃物,固体废弃物的堆积不仅造成资源的浪费,还会大面积侵占耕地,带来严重的环境污染和生态破坏。蓝晶石选矿尾矿储量以每年数万吨的速率增长,但是对于蓝晶石选矿尾矿仍未得到有效的解决途径。
耐火材料是高温设备内使用的结构材料,是实现高温的技术工艺和保护炉体结构的长期稳定工作的基础材料。其中,氮化硅结合碳化硅是一种新型的高级耐火材料,它具有硬度高、强度高、热稳定性好以及热震稳定性好、使用寿命长、高温抗蠕能力强、耐腐蚀、耐极冷极热、抗氧化等优势,广泛应用于钢铁、有色金属、化工建材等多种行业。此外,SiC结合Sialon是在高炉内衬的SiC材料的基础上发展起来的,也具有高的抗氧化性、抗侵蚀性能等优点,也具有广泛的应用前景。但是这类复相耐高温材料存在制备工艺复杂以及成本高等缺点,其技术工艺亟需改进提升。本发明专利结合上述突出问题,提出采用蓝晶石选矿尾矿作为原料,通过碳热还原氮化实现低成本转型转相制备Sialon-SiC复相粉体,并利用它替代Si3N4-SiC复相材料中的部分Si3N4,获得新型Sialon/Si3N4-SiC复相耐高温材料,具有较好的力学性能,能够满足钢铁冶炼行业耐高温材料、陶瓷部件等使用要求,也为实现蓝晶石选矿尾矿等固体废弃物的综合利用提供了新途径。
发明内容:
本发明的目的是针对目前钢铁冶金新技术新工艺对高性能耐火材料苛刻性能的迫切要求以及铝硅质复相耐高温材料制备成本高等突出问题,结合蓝晶石选矿尾矿利用程度低的突出瓶颈问题,提出一种以蓝晶石选矿尾矿转型转相得到的Sialon-SiC复相粉体和Si3N4、SiC等为原料制备新型Sialon/Si3N4-SiC复相耐高温材料的新工艺。
为实现上述目的,本发明的技术方案如下:
本发明是一种利用蓝晶石选矿尾矿转型转相制备Sialon/Si3N4-SiC复相耐高温材料的方法,其特征在于:采用蓝晶石选矿尾矿、碳质材料和高纯氮气为主要原料,经配料、球磨混料、高温碳热还原氮化反应、磨细、除碳等工艺进行处理,制备得到纯度较高Sialon-SiC复相粉体;采用制得的Sialon-SiC复相粉体以及商用Si3N4粉体和SiC粉体为主要原料,经配料、混料、成型、高温非氧化保护气氛烧结等工艺,制备得到Sialon/Si3N4-SiC复相耐高温材料。
本发明提出的一种利用蓝晶石选矿尾矿转型转相制备Sialon/Si3N4-SiC复相耐高温材料的方法,其特征在于:其中蓝晶石选矿尾矿为工业废弃物,其主要成分为氧化铝含量20-50%,二氧化硅含量50-80%,少量K2O、Fe2O3等杂质;Si3N4材料为市售工业原料,其质量要求为Si3N4的含量大于85%,氧化铁含量小于1.5%,其他杂质总含量小于8%,粒度小于20mm;SiC材料为市售工业原料,其质量要求SiC含量大于95.0%,氧化铁含量小于1.5%,粒度小于5.0mm。碳质材料为市售工业原料,其质量要求为含碳量80%,灰分不大于8%,挥发分不大于7%,含硫量小于2%,水分不大于5%,粒度小于20mm。发明所用碳源为焦炭、炭黑或无烟煤等,其理论配碳量按照原料中氧化物完全反应计算得到;氮化气氛由氮气提供,气氛的压力为1Pa-10Pa;碳热还原氮化的反应温度为1000℃-1800℃,反应时间2-20h;除碳温度为600℃-700℃,反应时间为1-3h;反应得到的Sialon-SiC复相粉体主要成分为Sialon和SiC,其含量高于90wt%。发明制备Sialon/Si3N4-SiC复相耐高温材料的配方为碳热还原氮化制得的Sialon-SiC复相粉体占总配料的质量比为0-30%,碳化硅粉体占总配料的质量比为70%,氮化硅粉体占总配料的质量比为0-30%;经配料、混料、干压成型、冷等静压处理、保护气氛烧结等工艺制备得到该复相耐高温材料;非氧化保护气氛由高纯氮气或氩气实现,烧结温度为1200℃-1700℃、保温时间2-20小时。
具体实施方式:
下面以具体实施例进一步阐述本发明的技术方案,但并非仅仅局限于下述实施案例。
实施例1
原料:
蓝晶石选矿尾矿为工业废弃物,其主要成分为氧化铝含量20-50%,二氧化硅含量50-80%,少量K2O,Fe2O3等杂质。
Si3N4材料为市售工业原料,其质量要求为Si3N4的含量大于85%,氧化铁含量小于1.5%,其他杂质总含量小于8%,粒度小于20mm;
SiC材料为市售工业原料,其质量要求SiC含量大于95.0%,氧化铁含量小于1.5%,粒度小于5.0mm。
碳质材料为焦炭颗粒,市售工业原料,其质量要求为含碳量80%,灰分不大于8%,挥发分不大于7%,含硫量小于2%,水分不大于5%,粒度小于20mm。
将上述材料中的蓝晶石选矿尾矿和焦炭分别研磨后过100目筛,按照比例称量后放入球磨罐中,干混12小时,将球磨后的粉体倒入钢模中,利用粉末压片机,进行干压成型。
采用碳热还原氮化法,将干压成型的粉体放入高纯氧化铝坩埚中,采用焦炭颗粒埋碳,并在氮气气氛下于1550℃下保温4小时。
将烧结后的试样破碎,放入研钵中研磨成细粉,为Sialon-SiC复相粉体。
将Sialon-SiC复相粉体、Si3N4粉体、不同粒级的SiC粉体按照比例称量后倒入钢模中,利用粉末压片机压成4×4×3mm的条状试样,进行冷等静压处理。
Sialon-SiC复相粉体占总质量分数的25%,Si3N4325目粉体占总质量分数的5%,325目SiC粉体占总质量分数的28%,240目SiC粉体占总质量分数的21%,21目SiC粉体占总质量分数的21%。
将上述条状试样放入氧化铝坩埚中,在氮气气氛、压力为0.04MPa下于1550℃下保温4小时进行低压烧结。保温结束后,随炉膛冷却至室温,得到Sialon/Si3N4-SiC复相粉体。
所得的Sialon/Si3N4-SiC复相粉体其抗折强度为40.59MPa,抗压强度为63.06MPa。
实施例2
原料:
蓝晶石选矿尾矿为工业废弃物,其主要成分为氧化铝含量20-50%,二氧化硅含量50-80%,少量K2O,Fe2O3等杂质。
Si3N4材料为市售工业原料,其质量要求为Si3N4的含量大于85%,氧化铁含量小于1.5%,其他杂质总含量小于8%,粒度小于20mm
SiC材料为市售工业原料,其质量要求SiC含量大于95.0%,氧化铁含量小于1.5%,粒度小于5.0mm。
碳质材料为无烟煤,市售工业原料,其质量要求为含碳量90%,灰分不大于4%,挥发分不大于3%,含硫量小于2%,水分不大于1%,粒度小于20mm。
将上述材料中的蓝晶石选矿尾矿和无烟煤分别研磨后过100目筛,按照比例称量后放入球磨罐中,干混12小时,将球磨后的粉体倒入钢模中,利用粉末压片机,进行干压成型。
采用碳热还原氮化法,将干压成型的粉体放入高纯氧化铝坩埚中,采用焦炭颗粒埋碳,并在氮气气氛下于1550℃下保温4小时。
将烧结后的试样破碎,放入研钵中研磨成细粉,为Sialon-SiC复相粉体。
将Sialon-SiC复相粉体、Si3N4粉体、不同粒级的SiC粉体按照比例称量后倒入钢模中,利用粉末压片机压成4×4×3mm的条状试样,进行冷等静压处理。Sialon-SiC复相粉体占总质量分数的20%,Si3N4325目粉体占总质量分数的10%,325目SiC粉体占总质量分数的28%,240目SiC粉体占总质量分数的21%,21目SiC粉体占总质量分数的21%。
将上述条状试样放入氧化铝坩埚中,在氮气气氛、压力为0.04MPa下于1550℃下保温4小时进行低压烧结。保温结束后,随炉膛冷却至室温,得到Sialon/Si3N4-SiC复相粉体。
所得的Sialon/Si3N4-SiC复相粉体其抗折强度为37.43MPa,抗压强度为50.02MPa。
实施例3
原料:
蓝晶石选矿尾矿为工业废弃物,其主要成分为氧化铝含量20-50%,二氧化硅含量50-80%,少量K2O,Fe2O3等杂质。
Si3N4材料为市售工业原料,其质量要求为Si3N4的含量大于85%,氧化铁含量小于1.5%,其他杂质总含量小于8%,粒度小于20mm;
SiC材料为市售工业原料,其质量要求SiC含量大于95.0%,氧化铁含量小于1.5%,粒度小于5.0mm。
焦炭材料为市售工业原料,其质量要求为含碳量80%,灰分不大于8%,挥发分不大于7%,含硫量小于2%,水分不大于5%,粒度小于20mm。
将上述材料中的蓝晶石选矿尾矿和焦炭分别研磨后过100目筛,按照比例称量后放入球磨罐中,干混12小时,将球磨后的粉体倒入钢模中,利用粉末压片机,进行干压成型。
采用碳热还原氮化法,将干压成型的粉体放入高纯氧化铝坩埚中,采用焦炭颗粒埋碳,并在氮气气氛下于1400℃下保温6小时。
将烧结后的试样破碎,放入研钵中研磨成细粉,为Sialon-SiC复相粉体。
将Sialon-SiC复相粉体、Si3N4粉体、不同粒级的SiC粉体按照比例称量后倒入钢模中,利用粉末压片机压成4×4×3mm的条状试样,进行冷等静压处理。Sialon-SiC复相粉体占总质量分数的15%,Si3N4325目粉体占总质量分数的15%,325目SiC粉体占总质量分数的28%,240目SiC粉体占总质量分数的21%,21目SiC粉体占总质量分数的21%。
将上述条状试样放入氧化铝坩埚中,在氮气气氛、压力为0.04MPa下于1600℃下保温3小时进行低压烧结。保温结束后,随炉膛冷却至室温,得到Sialon/Si3N4-SiC复相粉体。
所得的Sialon/Si3N4-SiC复相粉体其抗折强度为34.59MPa,抗压强度为47.86MPa。
Claims (7)
1.一种利用蓝晶石选矿尾矿转型转相制备Sialon/Si3N4-SiC复相耐高温材料的方法,其特征是采用蓝晶石选矿尾矿、碳质材料和高纯氮气为主要原料,经配料、球磨混料、高温碳热还原氮化反应、磨细、除碳等工艺进行处理,制备得到纯度较高Sialon-SiC复相粉体;采用制得的Sialon-SiC复相粉体以及商用Si3N4粉体和SiC粉体为主要原料,经配料、混料、成型、高温非氧化保护气氛烧结等工艺,制备得到Sialon/Si3N4-SiC复相耐高温材料。
2.根据权利要求1所述的主要原料,其特征在于:其中蓝晶石选矿尾矿为工业废弃物,其主要成分为氧化铝含量20-50%,二氧化硅含量50-80%,少量K2O、Fe2O3等杂质;Si3N4材料为市售工业原料,其质量要求为Si3N4的含量大于85%,氧化铁含量小于1.5%,其他杂质总含量小于8%,粒度小于20mm;SiC材料为市售工业原料,其质量要求SiC含量大于95.0%,氧化铁含量小于1.5%,粒度小于5.0mm。碳质材料为市售工业原料,其质量要求为含碳量80%,灰分不大于8%,挥发分不大于7%,含硫量小于2%,水分不大于5%,粒度小于20mm。
3.根据权利要求1所述的Sialon-SiC复相粉体制备工艺,其特征在于:所用碳源为焦炭、炭黑或无烟煤等,其理论配碳量按照原料中氧化物完全反应计算得到;氮化气氛由氮气提供,气氛的压力为1Pa-10Pa;碳热还原氮化的反应温度为1000℃-1800℃,反应时间2-20h;除碳温度为600℃-700℃,反应时间为1-3h。
4.根据权利要求1所述制备方法制得的Sialon-SiC复相粉体,其特征在于:Sialon-SiC复相粉体的主要成分为Sialon和SiC,其含量高于90wt%。
5.根据权利要求1所述的Sialon/Si3N4-SiC复相耐高温材料的原料比例,其特征在于:碳热还原氮化制得的Sialon-SiC复相粉体占总配料的质量比为0-30%,碳化硅粉体占总配料的质量比为70%,氮化硅粉体占总配料的质量比为0-30%。
6.根据权利要求1所述的Sialon/Si3N4-SiC复相耐高温材料的制备工艺,其特征在于:非氧化保护气氛由高纯氮气或氩气实现,烧结温度为1200℃-1700℃、保温时间2-20小时。
7.根据权利要求1所述的Sialon/Si3N4-SiC复相耐高温材料,其特征在于:制备得到的Sialon/Si3N4-SiC复相耐高温材料抗折强度高于30MPa,抗压强度高于40MPa,可用于耐高温材料、陶瓷部件等领域。
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