JPS6213082B2 - - Google Patents
Info
- Publication number
- JPS6213082B2 JPS6213082B2 JP9297778A JP9297778A JPS6213082B2 JP S6213082 B2 JPS6213082 B2 JP S6213082B2 JP 9297778 A JP9297778 A JP 9297778A JP 9297778 A JP9297778 A JP 9297778A JP S6213082 B2 JPS6213082 B2 JP S6213082B2
- Authority
- JP
- Japan
- Prior art keywords
- rolling
- oil
- emulsion
- water
- cold
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000005096 rolling process Methods 0.000 claims description 64
- 229910000831 Steel Inorganic materials 0.000 claims description 41
- 239000010959 steel Substances 0.000 claims description 41
- 239000000839 emulsion Substances 0.000 claims description 27
- 150000001875 compounds Chemical class 0.000 claims description 22
- 238000005097 cold rolling Methods 0.000 claims description 16
- 239000003995 emulsifying agent Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 239000010960 cold rolled steel Substances 0.000 claims description 5
- 239000000314 lubricant Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 description 25
- 235000014113 dietary fatty acids Nutrition 0.000 description 22
- 239000000194 fatty acid Substances 0.000 description 22
- 229930195729 fatty acid Natural products 0.000 description 22
- -1 amino fatty acids Chemical class 0.000 description 19
- 239000010731 rolling oil Substances 0.000 description 16
- 150000004665 fatty acids Chemical class 0.000 description 14
- 239000003921 oil Substances 0.000 description 14
- 235000019198 oils Nutrition 0.000 description 14
- 150000002148 esters Chemical class 0.000 description 8
- 238000005461 lubrication Methods 0.000 description 7
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000005554 pickling Methods 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000010775 animal oil Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 description 4
- 239000008158 vegetable oil Substances 0.000 description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 239000005639 Lauric acid Substances 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 230000001804 emulsifying effect Effects 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 235000015278 beef Nutrition 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 239000008235 industrial water Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 230000003134 recirculating effect Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- CFQZKFWQLAHGSL-FNTYJUCDSA-N (3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acid Chemical compound OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C CFQZKFWQLAHGSL-FNTYJUCDSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 241000316887 Saissetia oleae Species 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 125000005472 straight-chain saturated fatty acid group Chemical group 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Metal Rolling (AREA)
- Heat Treatment Of Sheet Steel (AREA)
Description
本発明は従来の冷延鋼板の製造における熱延鋼
板を酸洗後に冷間圧延する方式の酸洗過程を省略
して、熱延鋼板をスケールがついたまま直接冷間
圧延する新方式を実用可能にならしめるための冷
延鋼板の製造方法に関するものである。
従来の冷延鋼板の製造においてはそのほとんど
が熱延鋼板を硫酸や塩酸で酸洗を行い、熱間仕上
げ及び巻取り時に発生したスケールをほぼ完全に
除去した後に冷間圧延が行なわれる。この方式は
鉄鋼製造における永い歴史を持ち、冷間圧延前に
熱延鋼板の黒皮スケールを除去する事は常識とな
つていた。
しかるに最近に至りスケールがついたままの熱
延鋼板を直接冷間圧延する新方式が提案され研究
されている。例えば特開昭52―21245号、特開昭
52―21246号、特開昭52―52157号、特開昭52―
52158号公報等において提案された方法がこれに
相当するものである。
この無酸洗でスケールがついたまま直接冷間圧
延する新方式(以後直接冷延法と呼ぶ)は、酸洗
を省略する事によつて鋼板の製造設備の短縮化、
省力、省エネルギー、作業環境の向上をはかれる
と共に、廃酸設備が不要になる、等大きな利点が
ある。
一方直接冷延法については圧延時の圧延油の汚
染が著しい事、冷間圧延中あるいは圧延以後の過
程でいかにしてスケールを簡易に除去するかとい
う事、スケールを酸洗除去した場合に比べて圧延
時の荷重が増大する事及び圧延用ロールの摩耗量
が増大してしかも疵が発生しやすい事、などの問
題点が残されている。
本発明は上述の問題点において圧延荷重の軽
減、ロール摩耗量及びロール疵の軽減を計る事を
目的にしている。
前記した如く直接冷延法ではスケールが付着し
たままで冷間圧延するのであるが、このスケール
層は鋼板の地鉄より摩耗係数が大きいため酸洗鋼
板を圧延する場合に比べて圧延荷重が増大する。
さらにスケールの硬度が鋼板地鉄より高いためロ
ールの摩耗量が増大し、ロール疵も発生しやす
い。
これらの問題を解決するために本発明者等は圧
延潤滑方法について研究したところ、これらの問
題を一挙に解決する方法を見い出した。
圧延潤滑法について説明する。
従来、酸洗鋼板を冷間圧延する場合には一般に
高度の潤滑性が要求される極薄鋼板の圧延では動
植物油等の油脂を熱水と強制撹拌して乳化した10
〜20%の高濃度エマルジヨン油をスプレーするダ
イレクト適用法が多い。一方それほど高度の潤滑
性が要求されない板厚が比較的厚い場合の圧延に
は鉱物油と油脂の混合物を主成分としてこれに乳
化剤を配合したものを熱水で乳化した5%以下の
低濃度のエマルジヨン圧延油をリサーキユレート
適用する方式が多い。
そこで直接冷延法についても従来方式による潤
滑法で圧延を行つたところ以下の問題点がある事
がわかつた。即ち乳化剤を配合した低濃度エマル
ジヨン圧延油によるリサーキユレート圧延を行つ
たところ、酸洗鋼板の圧延の場合に比べて圧延荷
重が大巾に上昇する事、又圧延ロールの表面が荒
れて摩耗が大きい事、ロール表面に疵が発生しや
すい事、などが明らかになつた。又動植物油の高
濃度エマルジヨン圧延油によるダイレクト圧延を
行つた場合でも、乳化剤を含む低濃度エマルジヨ
ン油ほどではないが圧延荷重の上昇が認められ又
ロール表面の荒れ及び疵も発生する事が明らかに
なつた。
これらの問題点を解決するために圧延潤滑方法
を研究した結果、冷間圧延前又は冷間圧延中の熱
延鋼板の表面に有機極性化合物を主成分としか
つ、乳化剤を含有しない組成物を供給しておい
て、従来のエマルジヨン圧延油を用いて圧延する
とエマルジヨン圧延油だけで圧延した場合に比べ
て圧延潤滑性が大巾に向上し、しかもロール摩耗
の軽減とロール疵の軽減にも有効である事がわか
つた。さらに有機極性化合物を上述したように供
給する事によつて水単独及び水に溶解若しくは分
散する潤滑液を使用しても圧延が可能である事が
判つた。
これらの効果の1例を圧延荷重測定結果につい
て第1図に示した。第1図の結果から有機極性化
合物を塗布する事によつて圧延潤滑性が向上する
事が明らかである。
乳化剤を含有しない有機極性化合物を適用する
事によつて潤滑性が向上する理由は次の様に考え
られる。先ず有機極性化合物自体が鋼板表面に対
する吸着力が強く潤滑性が良い事と、乳化剤が含
まれていないので圧延時に乳化除去される心配が
ない事があげられる。従つて鋼板表面に圧延潤滑
に必要な量が存在すれば従来のエマルジヨン油に
比べて潤滑性が劣る水単独又は水に溶解若しくは
分散する潤滑液を用いても圧延する事が出来る。
而して、有機極性化合物を含む組成物は、圧延用
潤滑剤、例えばエマルジヨン圧延油を適用する以
前に鋼ストリツプ表面に適用されていなければな
らない。
次にエマルジヨン油による圧延の場合には次の
ように考えられる。乳化剤を含む低濃度エマルジ
ヨン圧延油を使用する場合には圧延油濃度が低い
事と、エマルジヨンが比較的安定なため圧延時の
スプレーによつて鋼板表面にぶつかつても破壊さ
れ難い事、によつて鋼板への圧延油の付着量が少
ないので潤滑性がやや劣る。そこで本発明による
極性化合物が存在する表面に対しては安定なエマ
ルジヨンでも吸着しやすいので圧延油の付着量が
多くなる事と極性化合物自体の潤滑性が良い事の
相乗効果により圧延潤滑性が向上するものと考え
られる。一方乳化剤を含まない動植物油等のの高
濃度エマルジヨン圧延油を使用する場合には圧延
油濃度が高い事とエマルジヨンが比較的不安定な
ためスプレーによつて鋼板にぶつかつた場合に破
壊されやすいので圧延油の付着量は多くなり潤滑
性は比較的優れている。しかしこの場合には鋼板
に対するスプレーパタンによる不均一塗布、及び
原料油脂成分の変動により乳化性が微秒に変化す
る事によつて付着量が変化するので潤滑性が不安
定になりやすくしかも潤滑性も十分とはいえな
い。そこで本発明による極性化合物が存在すると
潤滑性が向上するので、乳化性の変動による影響
も少なくなるものと考えられる。
以上説明したように本発明ではいずれも圧延前
又は、圧延中に乳化剤を含有しない非水溶性の有
機極性化合物を主成分とする組成物を供給する事
を主な要件としている。
本発明で使用する有機極性化合物について具体
的に説明する。
(イ) 脂肪酸:
牛脂、ナタネ油、等の動植物油の脂肪酸及びこ
れらの水素添加脂肪酸;ラウリン酸、その他の直
鎖飽和脂肪酸;オレイン酸、その他の不飽和脂肪
酸、ダイマー酸及びトリマー酸のような多塩基脂
肪酸;オキシ脂肪酸;アミノ脂肪酸;イソ脂肪
酸;合成脂肪酸;等が適当である。
(ロ) アミン:
ラウリルアミン、オレイルアミン、その他の飽
和又は不飽和の脂肪族アミン;この他ベンジルア
ミン、ジシクロヘキシルアミン等の芳香族アミ
ン、環状アミンも使用できる。さらにこれらのア
ミンと脂肪酸の反応で生成するアミンの脂肪酸塩
も使用できる。
(ハ) アルコール:
ラウリルアルコール、オレイルアルコール、そ
の他の飽和又は不飽和の脂肪族アルコール;及び
ベンジルアルコールのような芳香族のアルコール
も使用できる。この他脂肪族又は環状の多価アル
コールも使用できる。
(ニ) モノオールの脂肪酸エステル:
密ロウ、その他の天然ワツクスが適当である。
又高級一級アルコールと脂肪酸により合成したワ
ツクスも使用できる。
(ホ) ポリアルキレングリコールの脂肪酸エステ
ル:
ポリエチレングリコール脂肪酸エステル及びポ
リプロピレングリコール脂肪酸エステルが適当で
ある。
(ヘ) ネオペンチル核を有するポリオールの脂肪酸
エステル:
ペンタエリスリトール、ジペンタエリスリトー
ル、ネオペンチルグリコール、トリメチロールエ
タン、トリメチロールプロパン等の脂肪酸部分エ
ステル又は脂肪酸飽和エステルの単味及び2種以
上の混合物が適当である。エステル化に使用する
脂肪酸としては(イ)で説明したものが適当である。
(ト) 1分子中にOH基を3ケ以上有し且つネオペ
ンチル核を有しないポリオールの脂肪酸エステ
ル:
グリセリン、ポリグリセリン、マンニトール、
アンヒドロソルビトール、などの脂肪酸部分エス
テル又は脂肪酸飽和エステルの単味及び2種以上
の混合物が適当である。エステル化に使用する脂
肪酸としては(イ)で説明したものが適当である。
(チ) 燐酸エステル:
アルキル燐酸エステル、アルキルアリル燐酸エ
ステル、ポリオキシエチレンアルキルアリルエー
テルの燐酸エステル、ポリオキシエチレンアルキ
ルエーテルの燐酸エステル、ポリオキシエチレン
脂肪酸の燐酸エステル等が適当である。
(リ) 硼酸エステル:
硼酸とモノアルコール又は多価アルコールより
生成される硼酸部分エステル、飽和エステル、及
びこれらの混合物が適当である。以上9種に大別
したがこれら以外の有機極性化合物でも潤滑性が
優れた化合物であれば同様に使用する事ができ
る。
極性化合物は100%に近い純度で使用する場合
に潤滑性は最も良いが、コストを下げるために、
他の非極性化合物で希釈することもできる。希釈
剤としてはたとえば鉱物油が最も実用的である。
塗布量は、極性化合物として、0.05g/m2以上で
あれば潤滑性の向上に効果が認められ、塗布量が
多いほど好ましいが経済的には0.05g〜3g/m2
が適当である。
又極性化合物を供給する方法としては圧延前に
供給する場合にはスプレー塗布、静電スプレー塗
布、ロールコーター塗布、圧延前にスキンパスを
行う際に塗布する等のような方法でも良く冷間圧
延前の鋼板に塗布されておれば良い。
一方冷間圧延中に供給する場合には圧延ロール
にスプレー又はその他の方法で塗布する事によつ
て鋼板へ転写する方法、圧延中にスタンド間で直
接鋼板にスプレー又はその他の方法で塗布する事
もできる。圧延中に供給する場合には全パスでの
適用、又は特定のパスで適用しても良いが潤滑性
と作業性の点では第1パス前面でロールに供給す
るか第1パス後に鋼板表面に供給するのが最も好
ましい。
本発明を実施例について説明する。
試験条件を以下に説明する。
(イ) 供試鋼板
JISに規定するSPCC冷延鋼板製造用の熱延鋼
板を生産工場で採取して圧延試験用に2.3mm(板
厚)×50mm(巾)×100mm(長さ)の寸法で剪断し
たものを使用した。酸洗鋼板は工場採取材を実験
室で酸洗してスケールを除去した。
(ロ) 圧延条件
1 圧延機 ;11スタンド、レバーシングミル
2 ロール寸法;460mm(直径)
×100mm(胴長)
3 圧延速度 ;250m/分
4 極性化合物の供給法
圧延前に供給する方法としては塗装用のスプレ
ーガンを用いて鋼板表面に直接スプレー塗布し
た。一方圧延中に供給する方法としては第1パス
の前面でロール面にスプレーガンを用いて塗布し
て圧延する事によつて鋼板面に転写させた。なお
極性化合物の中で常温で固形のものについては加
熱溶融しておいてスプレーした。
5 圧延潤滑剤
(a) 水単独
工業用水を20〜25℃で使用して圧延ロールの材
料吸込み口にスプレーした。
(b) 水溶性、水分散性の潤滑剤
工業用水に溶解又は分散させて20〜25℃で使用
して圧延ロールの材料吸込み口にスプレーした。
(c) 低濃度エマルジヨン油
鉱物油を60%含有し、乳化剤を配合した市販の
乳化タイプの圧延油を3%エマルジヨンにして50
℃で使用。エマルジヨン油を循環させながら圧延
ロールの材料吸込み口にスプレーした。
(d) 高濃度エマルジヨン
市販の牛脂を強力に撹拌して20%エマルジヨン
油にして80℃で使用。エマルジヨン油を圧延前面
で鋼板にスプレーして非循環使用した。
(ハ) 圧延荷重の測定
各々の潤滑条件に応じて1パスでの圧下率が30
%になるようにロール間隙を設定しておいて圧延
時の全荷重をロードセルで測定した。次いでこの
荷重を圧延試験片巾50mmで除したKg/mmで表示し
た。
(ニ) ロール摩耗の測定
次の第1表の圧延スケジユールで各々の潤滑条
件ごとに100枚の試験片を圧延した後ロールの表
面レプリカを採取し、顕微鏡観察して表面の肌荒
れおよび摩耗状況を判定した。
The present invention has put into practical use a new method of directly cold rolling hot rolled steel sheets with scales attached, by omitting the pickling process of the conventional method of manufacturing cold rolled steel sheets, in which hot rolled steel sheets are pickled and then cold rolled. The present invention relates to a method for manufacturing cold-rolled steel sheets. In most conventional production of cold-rolled steel sheets, hot-rolled steel sheets are pickled with sulfuric acid or hydrochloric acid to almost completely remove scale generated during hot finishing and coiling, and then cold rolling is performed. This method has a long history in steel manufacturing, and it has become common knowledge to remove black scale from hot-rolled steel sheets before cold rolling. However, recently, a new method of directly cold rolling hot-rolled steel sheets with scales still attached has been proposed and researched. For example, JP-A-52-21245, JP-A-Sho.
No. 52-21246, JP-A No. 52-52157, JP-A No. 52-
The method proposed in Publication No. 52158 and the like corresponds to this. This new method (hereinafter referred to as the direct cold rolling method), in which the scale is directly cold rolled with no pickling, shortens the manufacturing equipment for steel sheets by omitting pickling.
It has great advantages such as saving labor and energy, improving the working environment, and eliminating the need for waste acid equipment. On the other hand, regarding the direct cold rolling method, there are problems such as the contamination of the rolling oil during rolling is significant, how to easily remove scale during cold rolling or in the process after rolling, and compared to the case where scale is removed by pickling. However, there remain problems such as an increase in the load during rolling, an increase in the amount of wear on the rolling rolls, and the tendency for flaws to occur. The present invention aims to solve the above-mentioned problems by reducing rolling load, roll wear, and roll flaws. As mentioned above, in the direct cold rolling method, cold rolling is performed with scale still attached, but since this scale layer has a higher wear coefficient than the base steel of the steel sheet, the rolling load is higher than when rolling a pickled steel sheet. do.
Furthermore, since the hardness of the scale is higher than that of the steel sheet base, the amount of roll wear increases and roll flaws are likely to occur. In order to solve these problems, the present inventors conducted research on rolling lubrication methods and found a method to solve these problems all at once. The rolling lubrication method will be explained. Conventionally, in the case of cold rolling pickled steel sheets, when rolling ultra-thin steel sheets that generally require a high degree of lubricity, oils such as animal and vegetable oils were forcibly stirred with hot water and emulsified10.
Direct application is often done by spraying a high concentration emulsion oil of ~20%. On the other hand, for rolling when the plate thickness is relatively thick and does not require a very high level of lubricity, a low concentration of 5% or less is made by emulsifying a mixture of mineral oil and oil as the main component with an emulsifier in hot water. Many methods use recirculating emulsion rolling oil. Therefore, when rolling was carried out using the conventional lubrication method for the direct cold rolling method, the following problems were found. That is, when recirculating rolling is performed using a low-concentration emulsion rolling oil containing an emulsifier, the rolling load increases significantly compared to the rolling of pickled steel sheets, and the surface of the rolling rolls becomes rough and wear increases. It became clear that the rolls were large and that scratches were likely to occur on the roll surface. Furthermore, even when direct rolling is performed using high-concentration emulsion rolling oil containing animal and vegetable oils, it is clear that the rolling load increases, although not as much as with low-concentration emulsion oil containing emulsifiers, and that roughness and flaws occur on the roll surface. Summer. As a result of research into rolling lubrication methods to solve these problems, we supplied a composition containing an organic polar compound as a main component and no emulsifier to the surface of hot rolled steel sheets before or during cold rolling. However, rolling with conventional emulsion rolling oil greatly improves rolling lubricity compared to rolling with emulsion rolling oil alone, and is also effective in reducing roll wear and roll flaws. I realized something. Furthermore, it has been found that by supplying the organic polar compound as described above, rolling is possible using water alone or a lubricating liquid dissolved or dispersed in water. An example of these effects is shown in FIG. 1 with respect to rolling load measurement results. From the results shown in FIG. 1, it is clear that rolling lubricity is improved by applying an organic polar compound. The reason why the lubricity is improved by applying an organic polar compound that does not contain an emulsifier is considered to be as follows. First, the organic polar compound itself has a strong adsorption force on the surface of the steel sheet and has good lubricity, and since it does not contain an emulsifier, there is no need to worry about the emulsification being removed during rolling. Therefore, as long as the amount necessary for rolling lubrication is present on the steel plate surface, rolling can be carried out using water alone or a lubricating liquid dissolved or dispersed in water, which has inferior lubricity compared to conventional emulsion oil.
Thus, the composition containing the organic polar compound must be applied to the steel strip surface prior to applying the rolling lubricant, such as emulsion rolling oil. Next, in the case of rolling using emulsion oil, the following can be considered. When using a low-concentration emulsion rolling oil containing an emulsifier, the rolling oil concentration is low and the emulsion is relatively stable, so it is difficult to be destroyed even if it hits the steel plate surface by spray during rolling. Since the amount of rolling oil attached to the steel plate is small, the lubricity is slightly inferior. Therefore, even a stable emulsion is easily adsorbed to the surface where the polar compound according to the present invention is present, so the rolling lubricity is improved due to the synergistic effect of increasing the amount of rolling oil attached and the good lubricity of the polar compound itself. It is considered that On the other hand, when using a high-concentration emulsion rolling oil such as animal or vegetable oil that does not contain an emulsifier, the concentration of the rolling oil is high and the emulsion is relatively unstable, so it is easily destroyed when it hits a steel plate by spraying. Therefore, the amount of rolling oil attached is large and the lubricity is relatively excellent. However, in this case, the lubricity tends to become unstable because the amount of adhesion changes due to non-uniform application due to the spray pattern on the steel plate, and the emulsifying property changes in a fraction of a second due to fluctuations in the raw material oil and fat components. is also not sufficient. Therefore, since the presence of the polar compound according to the present invention improves lubricity, it is thought that the influence of fluctuations in emulsifying property will be reduced. As explained above, the main requirement of the present invention is to supply a composition containing a water-insoluble organic polar compound as a main component that does not contain an emulsifier before or during rolling. The organic polar compound used in the present invention will be specifically explained. (b) Fatty acids: fatty acids of animal and vegetable oils such as beef tallow, rapeseed oil, etc. and their hydrogenated fatty acids; lauric acid and other straight chain saturated fatty acids; oleic acid and other unsaturated fatty acids, such as dimer acid and trimer acid. Polybasic fatty acids; oxyfatty acids; amino fatty acids; isofatty acids; synthetic fatty acids; etc. are suitable. (b) Amine: laurylamine, oleylamine, and other saturated or unsaturated aliphatic amines; aromatic amines and cyclic amines such as benzylamine and dicyclohexylamine can also be used. Furthermore, fatty acid salts of amines produced by the reaction of these amines and fatty acids can also be used. (c) Alcohol: Lauryl alcohol, oleyl alcohol, and other saturated or unsaturated aliphatic alcohols; and aromatic alcohols such as benzyl alcohol can also be used. In addition, aliphatic or cyclic polyhydric alcohols can also be used. (d) Monool fatty acid ester: Beeswax and other natural waxes are suitable.
Waxes synthesized from higher primary alcohols and fatty acids can also be used. (e) Fatty acid ester of polyalkylene glycol: Polyethylene glycol fatty acid ester and polypropylene glycol fatty acid ester are suitable. (f) Fatty acid esters of polyols having a neopentyl nucleus: Suitable are single fatty acid partial esters or fatty acid saturated esters such as pentaerythritol, dipentaerythritol, neopentyl glycol, trimethylolethane, trimethylolpropane, and mixtures of two or more. It is. As the fatty acid used for esterification, those explained in (a) are suitable. (g) Fatty acid esters of polyols having three or more OH groups in one molecule and not having a neopentyl nucleus: glycerin, polyglycerin, mannitol,
Single or mixtures of two or more fatty acid partial esters or fatty acid saturated esters such as anhydrosorbitol are suitable. As the fatty acid used for esterification, those explained in (a) are suitable. (H) Phosphate esters: Alkyl phosphates, alkylaryl phosphates, polyoxyethylene alkyl allyl ether phosphates, polyoxyethylene alkyl ether phosphoric esters, polyoxyethylene fatty acid phosphoric esters, and the like are suitable. (li) Boric acid ester: Boric acid partial esters produced from boric acid and monoalcohols or polyhydric alcohols, saturated esters, and mixtures thereof are suitable. Although the organic polar compounds are broadly classified into the above nine types, organic polar compounds other than these can be used in the same manner as long as they have excellent lubricity. Polar compounds have the best lubricity when used at a purity close to 100%, but to reduce costs,
It can also be diluted with other non-polar compounds. For example, mineral oil is the most practical diluent.
As for the coating amount, as a polar compound, if it is 0.05 g/m 2 or more, it is effective in improving lubricity, and the larger the coating amount is, the more preferable it is, but economically, it is 0.05 g/m 2 to 3 g/m 2
is appropriate. In addition, when supplying the polar compound before rolling, spray coating, electrostatic spray coating, roll coater coating, coating during skin pass before rolling, etc. may be used. It is sufficient if the coating is applied to the steel plate. On the other hand, when supplying during cold rolling, there are two methods: transfer to the steel plate by spraying or other methods on the rolling rolls, and directly applying the material to the steel sheet between stands during rolling. You can also do it. When feeding during rolling, it may be applied in all passes or in a specific pass, but in terms of lubricity and workability, it is best to feed it to the rolls in front of the first pass or to the surface of the steel plate after the first pass. Most preferably, it is supplied. The present invention will be described with reference to examples. The test conditions are explained below. (b) Test steel plate A hot-rolled steel plate for manufacturing SPCC cold-rolled steel plates specified in JIS was sampled at a production factory, and dimensions of 2.3 mm (thickness) x 50 mm (width) x 100 mm (length) were used for rolling tests. I used it after shearing it. The pickled steel plates were made from factory-collected material and were pickled in the laboratory to remove scale. (b) Rolling conditions 1 Rolling machine: 11 stands, levering mill 2 Roll dimensions: 460 mm (diameter) x 100 mm (body length) 3. Rolling speed: 250 m/min 4. Method of supplying polar compounds The method of supplying polar compounds before rolling is It was sprayed directly onto the surface of the steel plate using a paint spray gun. On the other hand, as a method of supplying it during rolling, it was applied to the roll surface using a spray gun on the front side of the first pass and was transferred to the steel plate surface by rolling. Among the polar compounds, those that are solid at room temperature were heated and melted before being sprayed. 5 Rolling Lubricant (a) Water alone Industrial water was used at 20-25°C and sprayed onto the material suction port of the rolling roll. (b) Water-soluble or water-dispersible lubricant The lubricant was dissolved or dispersed in industrial water and used at 20 to 25°C, and then sprayed onto the material suction port of a rolling roll. (c) Low concentration emulsion oil A commercially available emulsion type rolling oil containing 60% mineral oil and an emulsifier is made into a 3% emulsion.
Used at ℃. The emulsion oil was sprayed onto the material suction port of the rolling roll while being circulated. (d) Highly concentrated emulsion Commercially available beef tallow is vigorously stirred to make a 20% emulsion oil and used at 80℃. Emulsion oil was sprayed onto the steel plate at the front of the rolling mill and used in a non-circulating manner. (c) Measurement of rolling load The rolling reduction rate in one pass is 30 depending on each lubrication condition.
%, and the total load during rolling was measured using a load cell. Next, this load was divided by the width of the rolled test piece of 50 mm and expressed as Kg/mm. (d) Measurement of roll wear After rolling 100 test pieces under each lubrication condition according to the rolling schedule shown in Table 1 below, a replica of the roll surface was taken and observed under a microscope to determine the surface roughness and wear conditions. I judged it.
【表】
(ホ) ロール表面の疵発生度測定
前述の摩耗測定法で圧延した後のロール面につ
いて疵の発生程度を肉眼で観察して判定した。
以上の条件で実験した結果を第2表に実施例と
して示した。第2表からわかるように本発明によ
りスケール付きの熱延鋼板のまま直接圧延しても
酸洗鋼板と同様に圧延できロール摩耗及びロール
疵もほとんど問題ない。[Table] (e) Measurement of the degree of flaw occurrence on the roll surface The degree of flaw occurrence on the roll surface after rolling by the above-mentioned abrasion measuring method was determined by observing with the naked eye. The results of experiments conducted under the above conditions are shown in Table 2 as examples. As can be seen from Table 2, according to the present invention, even if the scaled hot-rolled steel sheet is directly rolled, it can be rolled in the same way as a pickled steel sheet, and there are almost no problems with roll wear and roll flaws.
【表】【table】
第1図は、本発明による極性化合物をスケール
付きの熱延鋼板(2.3mm(厚)×50mm(巾)×100mm
(長))にプレコートしておいて、水またはエマル
ジヨン圧延油を用いて冷間圧延を行ない、その際
の圧延荷重を測定した1例を、従来の酸洗工程を
経た鋼板の場合と比較図示したものである。
圧延条件
ロール寸法:460φ×100mm(胴長)
圧延速度 :250m/分
スケール付き熱延鋼板:3%エマルジヨン油によ
る圧延 …図中の符号1
醸洗熱延鋼板:3%エマルジヨン油による圧延
…図中の符号2
スケール付き熱延鋼板:ラウリン酸0.5g/m2塗
布後に水による圧延 …図中の符号3
スケール付き熱延鋼板:ラウリン酸0.5g/m2塗
布後3%エマルジヨン油による圧延
…図中の符号4
Figure 1 shows a scaled hot-rolled steel plate (2.3 mm (thickness) x 50 mm (width) x 100 mm) coated with the polar compound according to the present invention.
(Long)) is pre-coated and then cold-rolled using water or emulsion rolling oil, and the rolling load at that time was measured. This is compared with the case of a steel plate that has undergone a conventional pickling process. This is what I did. Rolling conditions Roll dimensions: 460φ x 100mm (body length) Rolling speed: 250 m/min Scaled hot-rolled steel sheet: Rolling with 3% emulsion oil...Reference number 1 in the diagram Brewing hot-rolled steel sheet: Rolling with 3% emulsion oil
...Number 2 in the figure Hot rolled steel sheet with scales: Rolled with water after applying lauric acid 0.5g/ m2 ...Number 3 in the figure Hot rolled steel sheet with scales: Rolling with 3% emulsion oil after applying lauric acid 0.5g/ m2 rolling
...Number 4 in the diagram
Claims (1)
延するに際し、有機極性化合物を主成分とし、且
つ乳化剤を含有しない非水溶性の組成物を冷間圧
延に先立つて塗布し、次いで、エマルジヨン圧延
油、水溶性若しくは水分散性潤滑剤および水のう
ちの少なくとも1種以上を供給して冷間圧延する
ことを特徴とする冷延鋼板の製造法。1. When cold rolling a hot rolled steel sheet with scale still attached, a water-insoluble composition containing an organic polar compound as a main component and containing no emulsifier is applied prior to cold rolling, and then emulsion rolling is performed. A method for producing a cold-rolled steel sheet, which comprises cold rolling by supplying at least one of oil, a water-soluble or water-dispersible lubricant, and water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9297778A JPS5519483A (en) | 1978-07-29 | 1978-07-29 | Production of cold rolled steel plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9297778A JPS5519483A (en) | 1978-07-29 | 1978-07-29 | Production of cold rolled steel plate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5519483A JPS5519483A (en) | 1980-02-12 |
JPS6213082B2 true JPS6213082B2 (en) | 1987-03-24 |
Family
ID=14069445
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9297778A Granted JPS5519483A (en) | 1978-07-29 | 1978-07-29 | Production of cold rolled steel plate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5519483A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105414179B (en) * | 2015-12-09 | 2017-06-16 | 安徽工业大学 | Improve cold rolling process of the ferrite stainless steel with structure property and its analysis method |
JP7316883B2 (en) * | 2019-08-30 | 2023-07-28 | 日本パーカライジング株式会社 | Cold rolling oil composition and method for producing rolled steel sheet using the same |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5221245A (en) * | 1975-08-13 | 1977-02-17 | Nippon Steel Corp | Method for colddrolling of steel |
-
1978
- 1978-07-29 JP JP9297778A patent/JPS5519483A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5519483A (en) | 1980-02-12 |
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