JP2009298633A - Casting monolithic refractory - Google Patents
Casting monolithic refractory Download PDFInfo
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- JP2009298633A JP2009298633A JP2008153863A JP2008153863A JP2009298633A JP 2009298633 A JP2009298633 A JP 2009298633A JP 2008153863 A JP2008153863 A JP 2008153863A JP 2008153863 A JP2008153863 A JP 2008153863A JP 2009298633 A JP2009298633 A JP 2009298633A
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- 238000005266 casting Methods 0.000 title abstract description 5
- 239000011823 monolithic refractory Substances 0.000 title abstract 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000004115 Sodium Silicate Substances 0.000 claims abstract description 19
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229910052911 sodium silicate Inorganic materials 0.000 claims abstract description 19
- 229910000318 alkali metal phosphate Inorganic materials 0.000 claims abstract description 17
- 239000011230 binding agent Substances 0.000 claims abstract description 17
- 239000011787 zinc oxide Substances 0.000 claims abstract description 13
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 238000002156 mixing Methods 0.000 abstract description 6
- 238000010276 construction Methods 0.000 description 23
- 230000000052 comparative effect Effects 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 238000000926 separation method Methods 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 239000002994 raw material Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 7
- 238000004898 kneading Methods 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000011819 refractory material Substances 0.000 description 5
- 239000004568 cement Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- -1 alkali metal carboxylates Chemical class 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052596 spinel Inorganic materials 0.000 description 3
- 239000011029 spinel Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 229910052582 BN Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229910026551 ZrC Inorganic materials 0.000 description 1
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- CAVCGVPGBKGDTG-UHFFFAOYSA-N alumanylidynemethyl(alumanylidynemethylalumanylidenemethylidene)alumane Chemical compound [Al]#C[Al]=C=[Al]C#[Al] CAVCGVPGBKGDTG-UHFFFAOYSA-N 0.000 description 1
- INJRKJPEYSAMPD-UHFFFAOYSA-N aluminum;silicic acid;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O INJRKJPEYSAMPD-UHFFFAOYSA-N 0.000 description 1
- 229910052849 andalusite Inorganic materials 0.000 description 1
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 description 1
- 239000003830 anthracite Substances 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052839 forsterite Inorganic materials 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 239000010443 kyanite Substances 0.000 description 1
- 229910052850 kyanite Inorganic materials 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 229910021382 natural graphite Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- OQZCJRJRGMMSGK-UHFFFAOYSA-M potassium metaphosphate Chemical compound [K+].[O-]P(=O)=O OQZCJRJRGMMSGK-UHFFFAOYSA-M 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 235000019828 potassium polyphosphate Nutrition 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052851 sillimanite Inorganic materials 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- ZVWKZXLXHLZXLS-UHFFFAOYSA-N zirconium nitride Chemical compound [Zr]#N ZVWKZXLXHLZXLS-UHFFFAOYSA-N 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
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- Ceramic Products (AREA)
- Furnace Housings, Linings, Walls, And Ceilings (AREA)
Abstract
Description
本発明は、流し込み不定形耐火物に関する。 The present invention relates to a cast amorphous refractory.
炉本体、樋、取鍋などにおいては、各種の高温溶融物と接触したり高温雰囲気に曝されるため、流し込み不定形耐火物により内張りすることが従来から行われている。不定形耐火物としては、アルミナセメントを使用するのが一般的であるが、混練後に短時間で硬化してしまうため、施工現場にミキサー等を持ち込んで、施工者が硬化しないように少量ずつ加水混練を行う必要があり、作業面やコスト面での問題がある。 In the furnace main body, the ladle, the ladle, etc., since it is in contact with various high-temperature melts or exposed to a high-temperature atmosphere, it has been conventionally performed to line with a cast amorphous refractory. Alumina cement is generally used as an amorphous refractory. However, since it hardens in a short time after kneading, bring a mixer etc. to the construction site and add water little by little to prevent the installer from hardening. It is necessary to perform kneading, and there are problems in terms of work and cost.
このため、特許文献1には、粉末珪酸塩とアルカリ金属リン酸塩とを所定の混合比で混合し、これを耐火性骨材に所定の割合で添加した後、水を加えて混練してなる熱硬化性流し込み耐火物が開示されている。この流し込み耐火物は、常温では硬化の進行が遅いため、予め工場で混練してから現場に運んで施工することができる。
ところが、特許文献1に開示された熱硬化性流し込み耐火物は、長期間の保管やトラック等での輸送中に、材料中の骨材が沈んで水が浮くという分離現象を生じることがあり、施工性の面で更に改良の余地があった。 However, the thermosetting cast refractory disclosed in Patent Document 1 may cause a separation phenomenon that the aggregate in the material sinks and the water floats during long-term storage or transportation by truck, There was room for further improvement in terms of workability.
そこで、本発明は、現場での施工性に優れる流し込み不定形耐火物の提供を目的とする。 Then, an object of this invention is to provide the casting unshaped refractory excellent in the construction property on the spot.
本発明者らは、鋭意研究の結果、珪酸ナトリウム及びアルカリ金属リン酸塩を含む結合剤を、耐火性骨材に添加した流し込み不定形耐火物において、結合剤として酸化亜鉛を更に加えることにより、加水混練の後に一旦硬化しても、振動を与えることで再び流動性を発現することを見出し、本願発明を完成するに至った。 As a result of diligent research, the present inventors have further added zinc oxide as a binder in a cast amorphous refractory in which a binder containing sodium silicate and an alkali metal phosphate is added to a refractory aggregate. Even after curing once after the hydro-kneading, it was found that the fluidity was developed again by applying vibration, and the present invention was completed.
すなわち、本発明の前記目的は、耐火性骨材100重量部に対する結合剤の添加割合が0.1〜10重量部であり、前記結合剤は、珪酸ナトリウム及びアルカリ金属リン酸塩を重量比で6:4〜2:8の割合で混合した混合物100重量部に対し、酸化亜鉛を0.05〜30重量部添加したことを特徴とする流し込み不定形耐火物により達成される。 That is, the object of the present invention is that the binder is added in an amount of 0.1 to 10 parts by weight with respect to 100 parts by weight of the refractory aggregate, and the binder includes sodium silicate and alkali metal phosphate in a weight ratio. This is achieved by a cast amorphous refractory characterized by adding 0.05 to 30 parts by weight of zinc oxide to 100 parts by weight of the mixture mixed at a ratio of 6: 4 to 2: 8.
本発明によれば、現場での施工性に優れる流し込み不定形耐火物を提供することができる。 According to the present invention, it is possible to provide a cast amorphous refractory having excellent workability on site.
本発明の流し込み不定形耐火物は、耐火性骨材に結合材を添加して生成される。 The cast amorphous refractory of the present invention is produced by adding a binder to a refractory aggregate.
(a)耐火性骨材
本発明に使用する耐火性骨材としては、(1) 電融アルミナ、焼結アルミナ、化焼アルミナなどの高アルミナ原料(2) 焼成ボーキサイト、ムライト、シリマナイト、カイヤナイト、アンダルサイトなどのアルミナ−シリカ原料(3) ロー石、シャモット、粘土質鉱物などのシリカ−アルミナ原料(4) 珪砂、珪石、溶融石英などの珪酸質原料(5) クロム鉄鉱、焼結スピネル、電融スピネルなどのスピネル原料(6) マグネシアクリンカー、フォルステライト、ドロマイトクリンカー、カルシアなどの塩基性原料(7) ジルコン質原料(8) ジルコニア質原料(9) 炭化珪素、炭化ジルコニウム、炭化アルミニウム、炭化硼素などの炭化物質原料(10)窒化珪素、窒化ジルコニウム、窒化硼素、窒化アルミニウムなどの窒化物質原料(11)コークス、天然黒鉛、人造黒鉛、無煙炭、カーボンブラック、カーボン煉瓦屑、電極屑などの炭素質原料(12)珪酸ソーダ塊、珪素、酸化クロムなどの耐火性粉末を使用可能である。また、耐火性骨材として、これら各群から1種または2種以上選択して利用することもでき、或いは、異なる群から1種又は2種以上選択して利用することもできる。耐火性骨材は、約5mm以下に粒度調整されていることが好ましい。
(A) Refractory Aggregate The refractory aggregate used in the present invention includes (1) high alumina raw materials such as fused alumina, sintered alumina, and calcined alumina (2) calcined bauxite, mullite, sillimanite, kyanite Alumina-silica raw materials such as andalusite (3) Silica-alumina raw materials such as rholite, chamotte and clay minerals (4) Silicic raw materials such as silica sand, silica and fused silica (5) Chromium iron ore, sintered spinel, Spinel raw materials such as fused spinel (6) Basic raw materials such as magnesia clinker, forsterite, dolomite clinker, calcia (7) Zircon material (8) Zirconia material (9) Silicon carbide, zirconium carbide, aluminum carbide, carbonized Boron and other carbide materials (10) Silicon nitride, zirconium nitride, boron nitride, aluminum nitride and other nitride materials (11) Coke, natural graphite, Concrete graphite, anthracite, carbon black, carbon brick scrap, carbonaceous feedstock (12) sodium silicate mass, such as an electrode scrap, silicon can be used for refractory powder such as chromium oxide. Further, as the refractory aggregate, one or more types can be selected and used from each of these groups, or one or more types can be selected and used from different groups. The refractory aggregate is preferably adjusted in particle size to about 5 mm or less.
(b)結合剤
結合剤としては、難溶性の粉末珪酸ナトリウムと、アルカリ金属リン酸塩とを含む混合物に、酸化亜鉛を添加したものを使用する。
(B) Binder As the binder, a mixture obtained by adding zinc oxide to a mixture containing hardly soluble powdered sodium silicate and alkali metal phosphate is used.
粉末珪酸ナトリウムは、SiO2を50〜80%、Na2Oを15〜40%含有するものを使用することが好ましい。SiO2とNa2Oのモル比は、特に限定されるものではないが、溶解度が小さすぎると硬化がし難くなる一方、溶解度が大きすぎると早く硬化して施工時の流動性が確保しにくいことから、20℃における溶解度が0.1〜5%程度となるように、適宜調整することが好ましい。 It is preferable to use a powdered sodium silicate containing 50 to 80% SiO 2 and 15 to 40% Na 2 O. The molar ratio of SiO 2 and Na 2 O is not particularly limited. However, if the solubility is too small, it is difficult to cure, whereas if the solubility is too large, the composition is cured quickly and it is difficult to ensure the fluidity during construction. Therefore, it is preferable to adjust appropriately so that the solubility at 20 ° C. is about 0.1 to 5%.
また、アルカリ金属リン酸塩は、リン酸ナトリウム、トリポリリン酸ナトリウム、テトラポリリン酸ナトリウム、リン酸カリウム、ポリリン酸カリウムなどを例示することができ、特に、トリポリリン酸二水素アルミニウムの水和物(AlH2P3O10・2H2O)を好ましく使用することができる。 Examples of the alkali metal phosphate include sodium phosphate, sodium tripolyphosphate, sodium tetrapolyphosphate, potassium phosphate, and potassium polyphosphate. In particular, hydrate of aluminum dihydrogen tripolyphosphate (AlH 2 P 3 O 10 · 2H 2 O) can be preferably used.
酸化亜鉛(ZnO)は、微粉末状であることが好ましく、珪酸ナトリウム及びアルカリ金属リン酸塩の混合物に、均一に分散される。また、使用する酸化亜鉛の純度は、90%以上であることが好ましい。 Zinc oxide (ZnO) is preferably in the form of fine powder, and is uniformly dispersed in a mixture of sodium silicate and alkali metal phosphate. Moreover, it is preferable that the purity of the zinc oxide to be used is 90% or more.
(c)混合割合
i)結合剤(珪酸ナトリウム、アルカリ金属リン酸塩、酸化亜鉛)
結合剤に含まれる珪酸ナトリウム及びアルカリ金属リン酸塩の混合比は、アルカリ金属リン酸塩の割合が大きすぎると、施工後に硬化し難く十分な強度が得られない一方、珪酸ナトリウムの割合が大きすぎると、流動性が悪化すると共に硬化が早く生じて施工が困難になる傾向になる。したがって、珪酸ナトリウム及びアルカリ金属リン酸塩を、重量比で6:4〜2:8の割合で混合することが好ましく、4:6〜2.5:7.5の割合で混合することがより好ましい。また、スラリーを構成する耐火性骨材等の粉体の粒度分布、粉体嵩等のばらつきは、加水混錬後のスラリーの性質にもばらつきを与え、施工性に悪影響を生ずる場合がある。このような原料粉体のばらつきにも影響されにくいという観点から、実用的に最も好ましい珪酸ナトリウム及びアルカリ金属リン酸塩の重量比は、1:約2.8である。
(C) Mixing ratio i) Binder (sodium silicate, alkali metal phosphate, zinc oxide)
As for the mixing ratio of sodium silicate and alkali metal phosphate contained in the binder, if the proportion of alkali metal phosphate is too large, it is difficult to cure after construction and sufficient strength cannot be obtained, while the proportion of sodium silicate is large. When too much, fluidity | liquidity will deteriorate, and it will become hard to produce early, and it will become the tendency for construction to become difficult. Therefore, it is preferable to mix sodium silicate and alkali metal phosphate in a weight ratio of 6: 4 to 2: 8, and more preferably in a ratio of 4: 6 to 2.5: 7.5. preferable. Moreover, the dispersion | distribution of the particle size distribution, powder bulk, etc. of powders, such as a refractory aggregate which comprises a slurry, will also have dispersion | variation also in the property of the slurry after hydromixing, and may have a bad influence on workability | operativity. From the viewpoint of being hardly affected by such variations in raw material powder, the most practically preferred weight ratio of sodium silicate and alkali metal phosphate is 1: about 2.8.
また、上記の混合物に添加する酸化亜鉛は、多すぎると、振動を与えても再び流動性を発現し難くなる一方、少なすぎると、生成される流し込み不定形耐火物に従来と同様の分離現象を生じるおそれがある。したがって、上記混合物100重量部に対し、酸化亜鉛を0.05〜30重量部添加することが好ましく、1〜25重量部添加することがより好ましい。 In addition, if too much zinc oxide is added to the above mixture, it will be difficult to develop fluidity again even if vibration is applied, while if too little, the generated separation-type refractory material will have the same separation phenomenon as before. May occur. Therefore, it is preferable to add 0.05-30 weight part of zinc oxide with respect to 100 weight part of the said mixture, and it is more preferable to add 1-25 weight part.
ii)耐火性骨材と結合剤
耐火性骨材に対する結合剤の割合は、小さすぎると、施工後に十分な強度が得られない一方、大きすぎると、施工後に十分な耐食性が得られない。したがって、耐火性骨材100重量部に対し、結合剤の添加割合を0.1〜10重量部とすることが好ましい。
ii) Refractory aggregate and binder If the ratio of the binder to the refractory aggregate is too small, sufficient strength cannot be obtained after construction, while if too large, sufficient corrosion resistance cannot be obtained after construction. Therefore, it is preferable that the addition ratio of the binder is 0.1 to 10 parts by weight with respect to 100 parts by weight of the refractory aggregate.
iii)その他
本発明の流し込み不定形耐火物は、本発明の効果を阻害しない範囲で、従来の流し込み不定形耐火物に使用されるものを添加してもよい。例えば、アルカリ金属カルボン酸塩、ポリカルボン酸系重合体、アルキルスルホン酸塩などの分散剤を使用することができる。
iii) Others The cast amorphous refractories of the present invention may be added to those used for conventional cast amorphous refractories as long as the effects of the present invention are not impaired. For example, dispersants such as alkali metal carboxylates, polycarboxylic acid polymers, and alkyl sulfonates can be used.
(d)使用方法
上記の流し込み不定形耐火物粉体は、予め工場などで適量の水を加えて混練することにより、1〜3日程度で自然硬化する。これにより、保存中や運搬中における水の分離現象を防止することができる。流し込み不定形耐火物に対する水の添加量は、例えば、流し込み不定形耐火物粉体100重量部に対して、5〜7重量部とすることができる。
(D) Method of use The above-mentioned cast amorphous refractory powder is naturally cured in about 1 to 3 days by adding an appropriate amount of water and kneading in advance at a factory or the like. Thereby, the separation phenomenon of water during storage or transportation can be prevented. The amount of water added to the cast amorphous refractory can be, for example, 5 to 7 parts by weight with respect to 100 parts by weight of the cast amorphous refractory powder.
ついで、加水混練後に硬化した流し込み不定形耐火物を、現場まで搬送し、施工直前にバイブレータ等で振動を与える。本発明の流し込み不定形耐火物は、結合剤中に酸化亜鉛が適量添加されているため、振動の付与によって、流動性を容易に発現させることができ、流し込み施工を行うことができる。 Next, the cast amorphous refractory cured after the hydro-kneading is transported to the site, and vibration is applied with a vibrator or the like immediately before construction. In the cast amorphous refractory according to the present invention, since an appropriate amount of zinc oxide is added to the binder, fluidity can be easily expressed by applying vibration, and casting can be performed.
流し込み施工の終了後、流し込み不定形耐火物の表面をバーナー等で加熱する。加熱条件は、例えば80〜100℃で3〜5時間程度である。このような強制加熱によって、難溶性の粉末珪酸ナトリウムは、溶解度が高まり、アルカリ金属リン酸塩と反応する。この結果、施工された流し込み不定形耐火物は、耐火材としての機能を十分発揮できる程度に硬化する。 After the pouring work is completed, the surface of the cast amorphous refractory is heated with a burner or the like. The heating conditions are, for example, about 80 to 100 ° C. and about 3 to 5 hours. By such forced heating, the poorly soluble powdered sodium silicate has increased solubility and reacts with the alkali metal phosphate. As a result, the poured cast refractory thus constructed is cured to such an extent that it can sufficiently function as a refractory material.
このように、本発明の流し込み不定形耐火物によれば、保存・運搬時には擬似的な硬化状態により水分離を抑制することができると共に、施工時には振動の付与により流動性を容易に発現させることができるので、施工性を良好にすることができる。 Thus, according to the cast amorphous refractory of the present invention, water separation can be suppressed by a pseudo-cured state during storage and transportation, and fluidity can be easily expressed by applying vibration during construction. Therefore, workability can be improved.
本発明の流し込み不定形耐火物は、各種金属、ガラス、セメント、スラグ、産業廃棄物等を溶解または処理するための高炉、キュポラ、アルミ、銅等およびその他の非鉄金属の溶解・保持炉、各種均熱炉、加熱炉、溝型または坩堝型等の電気誘導加熱炉、各種焼却炉、セメントキルン、ガラス溶解炉等の炉本体を初め、それらに付随した樋、取鍋、蓋、煙道、ダクト、ボイラー等の高温で用いる器具・装置において、各種の高温溶融物に接したり、高温雰囲気にさらされる部位を覆うために流し込み硬化させる目的で、好適に使用することができる。 The cast amorphous refractories of the present invention are blast furnaces for melting or treating various metals, glass, cement, slag, industrial waste, etc., melting / holding furnaces for various non-ferrous metals such as cupola, aluminum, copper, etc. Soaking furnace, heating furnace, grooved or crucible type electric induction heating furnace, various incinerators, cement kiln, glass melting furnace, etc. It can be suitably used for the purpose of pouring and curing in a device such as a duct or a boiler, which is used at a high temperature, so as to come into contact with various high-temperature melts or to cover a portion exposed to a high-temperature atmosphere.
以下に本発明の実施例及び比較例を挙げて、本発明を更に詳細に説明する。但し、本発明が以下の実施例に限定されるものではない。 Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples of the present invention. However, the present invention is not limited to the following examples.
流し込み不定形耐火物として、珪酸ナトリウム及びアルカリ金属リン酸塩の重量混合比をパラメータとして、各材料を表1に示す重量割合で混合したものを使用し、加水混練して混練直後のフロー値を測定すると共に、この混練物を長期保存し、7日後、14日後、21日後、28日後のフロー値をそれぞれ測定した。フロー値の測定は、JIS R2521(アルミナセメントのフロー試験)に準じて行い、流動性を発現させるため、測定直前にバイブレータによる振動を与えた。 As a cast amorphous refractory, using a weight mixing ratio of sodium silicate and alkali metal phosphate as a parameter, a mixture of each material in the weight ratio shown in Table 1, using water kneading, the flow value immediately after kneading While measuring, this kneaded material was stored for a long time, and the flow values after 7 days, 14 days, 21 days, and 28 days were measured. The flow value was measured according to JIS R2521 (alumina cement flow test), and vibration was applied by a vibrator immediately before the measurement in order to develop fluidity.
表1に示すように、比較例1及び実施例1〜4については、アルカリ金属リン酸塩に対して珪酸ナトリウムの割合が大きくなるにつれ、フロー値(すなわち流動性)が徐々に低下しているが、実施例4においても、28日後のフロー値は120以上を確保しており、長期保存後も振動の付与により良好な流動性を発現可能であった。一方、比較例2については、珪酸ナトリウムの割合が大きくなり過ぎて、保存期間が長期化すると流動性が急激に低下した、また、比較例3については、珪酸ナトリウムの割合が更に大きくなり、14日後には振動を与えても流動性を発現することはなく、施工が不可能な状態になった。 As shown in Table 1, in Comparative Example 1 and Examples 1 to 4, the flow value (ie, fluidity) gradually decreases as the proportion of sodium silicate with respect to the alkali metal phosphate increases. However, in Example 4, the flow value after 28 days was 120 or more, and good fluidity could be expressed by applying vibration even after long-term storage. On the other hand, for Comparative Example 2, the proportion of sodium silicate became too large, and the fluidity decreased sharply when the storage period was prolonged, and for Comparative Example 3, the proportion of sodium silicate was further increased. After the day, even if vibration was applied, fluidity did not appear and construction was impossible.
混練物の保存中は、耐火物原料に対して水が分離していないかを定期的に目視確認したが、実施例1〜4及び比較例1〜3のいずれも、分離現象は生じなかった。 During storage of the kneaded product, whether or not water was separated from the refractory raw material was regularly checked visually, but no separation phenomenon occurred in any of Examples 1-4 and Comparative Examples 1-3. .
混練物の保存開始から28日後に、バイブレータにより混練物に振動を与えて流動性を発現させてから、40×40×160(mm)の型枠に流し込み、60℃で3時間養生した後に脱枠して、施工性(流動性及び保形性)を評価した。 After 28 days from the start of storage of the kneaded product, the kneaded product was vibrated with a vibrator to develop fluidity, poured into a 40 × 40 × 160 (mm) mold, cured at 60 ° C. for 3 hours, and then removed. Frameability was evaluated for workability (fluidity and shape retention).
表1に示すように、実施例2〜3については、施工中の十分な流動性が確保されていると共に、施工後は硬化して十分な保形性が維持され、施工性は良好であった。また、実施例1は保形性が若干低下し、実施例4は流動性が若干低下しているものの、いずれも施工作業は可能であった。これに対し、比較例1は、施工後の十分な硬化強度が得られず、脱枠が困難であった。また、比較例2は、施工中の流動性が十分でなく、型枠への充填が困難であった。比較例3は、上記のとおり保存中に硬化してしまい、施工作業は不可能であった。 As shown in Table 1, in Examples 2 to 3, sufficient fluidity during construction was secured, and after construction, sufficient shape retention was maintained, and the workability was good. It was. Moreover, although the shape retention property of Example 1 was slightly lowered and the fluidity of Example 4 was slightly lowered, construction work was possible in all cases. On the other hand, in Comparative Example 1, sufficient curing strength after construction was not obtained, and it was difficult to remove the frame. In Comparative Example 2, the fluidity during the construction was not sufficient, and it was difficult to fill the mold. Comparative Example 3 was cured during storage as described above, and construction work was impossible.
次に、珪酸ナトリウム及びアルカリ金属リン酸塩の混合物に対する酸化亜鉛の重量混合比をパラメータとして、表1の場合と同様に、フロー値の測定、分離現象の目視、及び施工性の評価を行った。
Next, using the weight mixing ratio of zinc oxide to the mixture of sodium silicate and alkali metal phosphate as a parameter, the flow value was measured, the separation phenomenon was visually observed, and the workability was evaluated in the same manner as in Table 1. .
表2に示すように、比較例4及び実施例5〜9については、酸化亜鉛の割合が大きくなるにつれ、フロー値(すなわち流動性)が徐々に低下しているが、実施例9においても、28日後のフロー値は120以上を確保しており、長期保存後も振動の付与により良好な流動性を発現可能であった。一方、比較例5については、酸化亜鉛の割合が大きくなり過ぎたために、21日後には振動を与えても流動性を発現することはなく、施工が不可能な状態になった。 As shown in Table 2, for Comparative Example 4 and Examples 5 to 9, the flow value (ie, fluidity) gradually decreased as the proportion of zinc oxide increased, but also in Example 9, The flow value after 28 days secured 120 or more, and even after long-term storage, good fluidity could be expressed by applying vibration. On the other hand, in Comparative Example 5, since the ratio of zinc oxide became too large, fluidity was not expressed even after vibration was applied after 21 days, and the construction became impossible.
混練物の保存中は、実施例6〜9及び比較例5については、分離現象は生じなかった。実施例5は、若干の水浮きが生じるものの、施工作業は可能であった。一方、比較例4は、水の分離現象が生じやすく、十分撹拌しないと施工作業が行えない状態であった。 During the storage of the kneaded material, no separation phenomenon occurred in Examples 6 to 9 and Comparative Example 5. In Example 5, although some water floating occurred, construction work was possible. On the other hand, in Comparative Example 4, the water separation phenomenon was likely to occur, and the construction work could not be performed without sufficient stirring.
施工性については、実施例5〜8は、施工中の十分な流動性が確保されていると共に、施工後は硬化して十分な保形性が維持され、施工性は良好であった。実施例9は、流動性が若干低下しているものの、施工作業は可能であった。これに対し、比較例4は、上記のとおり水の分離現象が生じるために、十分な撹拌を行えば施工性は確保されるが、ミキサーなどを用いた煩雑な撹拌作業が必要であった。また、比較例5は、上記のとおり保存中に硬化してしまい、施工作業は不可能であった。 Regarding workability, Examples 5 to 8 ensured sufficient fluidity during construction, cured after construction, maintained sufficient shape retention, and had good workability. In Example 9, although the fluidity was slightly lowered, construction work was possible. On the other hand, in Comparative Example 4, since the water separation phenomenon occurs as described above, workability is ensured if sufficient stirring is performed, but complicated stirring work using a mixer or the like is necessary. Moreover, the comparative example 5 hardened | cured during storage as mentioned above, and construction work was impossible.
Claims (1)
前記結合剤は、珪酸ナトリウム及びアルカリ金属リン酸塩を重量比で6:4〜2:8の割合で混合した混合物100重量部に対し、酸化亜鉛を0.05〜30重量部添加したことを特徴とする流し込み不定形耐火物。
The addition ratio of the binder to 100 parts by weight of the refractory aggregate is 0.1 to 10 parts by weight,
In the binder, 0.05 to 30 parts by weight of zinc oxide is added to 100 parts by weight of a mixture in which sodium silicate and alkali metal phosphate are mixed at a weight ratio of 6: 4 to 2: 8. A pour-shaped amorphous refractory.
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JP2011213521A (en) * | 2010-03-31 | 2011-10-27 | Kurosaki Harima Corp | Castable refractory and method for manufacturing the same |
CN112010658A (en) * | 2019-05-28 | 2020-12-01 | 宝山钢铁股份有限公司 | Slag adhesion preventing material for refining ladle opening and preparation method thereof |
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