JPS6362824A - Heat treatment of rolled wire rod - Google Patents
Heat treatment of rolled wire rodInfo
- Publication number
- JPS6362824A JPS6362824A JP20671686A JP20671686A JPS6362824A JP S6362824 A JPS6362824 A JP S6362824A JP 20671686 A JP20671686 A JP 20671686A JP 20671686 A JP20671686 A JP 20671686A JP S6362824 A JPS6362824 A JP S6362824A
- Authority
- JP
- Japan
- Prior art keywords
- cooling
- bubbles
- water
- wire rod
- foam
- 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.)
- Granted
Links
- 238000010438 heat treatment Methods 0.000 title claims description 6
- 238000001816 cooling Methods 0.000 claims abstract description 82
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
- 239000004094 surface-active agent Substances 0.000 claims abstract description 19
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 16
- 238000000034 method Methods 0.000 claims description 23
- 239000004088 foaming agent Substances 0.000 claims description 11
- 239000004604 Blowing Agent Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 abstract description 7
- 229910000831 Steel Inorganic materials 0.000 abstract description 3
- 239000010959 steel Substances 0.000 abstract description 3
- 239000006185 dispersion Substances 0.000 abstract 1
- 239000006260 foam Substances 0.000 description 26
- 239000007864 aqueous solution Substances 0.000 description 11
- -1 fatty acid salts Chemical class 0.000 description 11
- 238000007654 immersion Methods 0.000 description 11
- 239000007789 gas Substances 0.000 description 8
- 239000003507 refrigerant Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- 239000012298 atmosphere Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000007664 blowing Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229910000639 Spring steel Inorganic materials 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 238000005098 hot rolling Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- AEQDJSLRWYMAQI-UHFFFAOYSA-N 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline Chemical compound C1CN2CC(C(=C(OC)C=C3)OC)=C3CC2C2=C1C=C(OC)C(OC)=C2 AEQDJSLRWYMAQI-UHFFFAOYSA-N 0.000 description 1
- URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 description 1
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 244000247812 Amorphophallus rivieri Species 0.000 description 1
- 235000001206 Amorphophallus rivieri Nutrition 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 102000004506 Blood Proteins Human genes 0.000 description 1
- 108010017384 Blood Proteins Proteins 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 108010076119 Caseins Proteins 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920002085 Dialdehyde starch Polymers 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229910000677 High-carbon steel Inorganic materials 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
- 229920002752 Konjac Polymers 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- FSVCELGFZIQNCK-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)glycine Chemical compound OCCN(CCO)CC(O)=O FSVCELGFZIQNCK-UHFFFAOYSA-N 0.000 description 1
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
- JYXGIOKAKDAARW-UHFFFAOYSA-N N-(2-hydroxyethyl)iminodiacetic acid Chemical compound OCCN(CC(O)=O)CC(O)=O JYXGIOKAKDAARW-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000004373 Pullulan Substances 0.000 description 1
- 229920001218 Pullulan Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005261 decarburization Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 229960004585 etidronic acid Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000000252 konjac Substances 0.000 description 1
- 235000010485 konjac Nutrition 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 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
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001444 polymaleic acid Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000000075 primary alcohol group Chemical group 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229960001790 sodium citrate Drugs 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- 239000000176 sodium gluconate Substances 0.000 description 1
- 235000012207 sodium gluconate Nutrition 0.000 description 1
- 229940005574 sodium gluconate Drugs 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000001433 sodium tartrate Substances 0.000 description 1
- 229960002167 sodium tartrate Drugs 0.000 description 1
- 235000011004 sodium tartrates Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 238000010301 surface-oxidation reaction Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/52—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
- C21D9/54—Furnaces for treating strips or wire
- C21D9/56—Continuous furnaces for strip or wire
- C21D9/573—Continuous furnaces for strip or wire with cooling
- C21D9/5732—Continuous furnaces for strip or wire with cooling of wires; of rods
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/56—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering characterised by the quenching agents
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/56—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering characterised by the quenching agents
- C21D1/60—Aqueous agents
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Heat Treatments In General, Especially Conveying And Cooling (AREA)
- Heat Treatment Of Strip Materials And Filament Materials (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は熱間圧延直後の高温線材を界面活性剤や水溶性
ポリマーでつくられる泡の中に浸漬する線材の熱処理方
法に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a wire heat treatment method in which a high-temperature wire immediately after hot rolling is immersed in a foam made of a surfactant or a water-soluble polymer.
(従来の技術)
熱間圧延直後の高温線材を急冷あるいは徐冷して熱処理
する方法として、空気、ミスト、水などを吹伺ける方法
、ソルトや鉛などの金属浴への浸るいは特開昭57−9
8213号に示されるような流動攪拌状態の温液体中へ
の浸漬法等、それぞれ用途に応じて用いられている。こ
れらの冷却技術はその大部分が単一機能ながら秀れた特
徴を持っているが、近年の鉄鋼製造技術の一傾向である
多品種小ロツト生産に対応するには、複数の冷却装置を
設置しなければならず、製造プロセスの複雑化や設備コ
ストの上昇を招く、この対策として1日本金属学会会報
第25巻第6号(198B) P、559に紹介されて
いるような多Jlj!、俺熱処理システムを生むに至っ
た。(Prior technology) As a heat treatment method by rapidly cooling or slowly cooling a high-temperature wire rod immediately after hot rolling, a method of blowing air, mist, water, etc., and a method of immersion in a metal bath of salt, lead, etc. are disclosed in Japanese Patent Publication No. Showa 57-9
Methods such as immersion in a hot liquid in a fluidized agitation state as shown in No. 8213 are used depending on the purpose. Most of these cooling technologies have excellent features despite having a single function, but in order to support the high-mix, small-lot production, which is a trend in recent steel manufacturing technology, it is necessary to install multiple cooling devices. As a countermeasure to this problem, a multi-Jlj! method is introduced in 1 Bulletin of the Japan Institute of Metals, Vol. 25, No. 6 (198B), p. 559. This led to the creation of the heat treatment system.
このシステムの特徴は10℃/S以下の冷却速度に対し
ては空冷方式、それ以上には浸漬方式を採用するもので
、その設備は上下2ライン構造とし、浸漬ラインには流
動攪拌状態で冷却するための冷媒循環装置等を持ってい
る。また、空冷ラインには保温カバー、ブロワ−を附設
し、所望の冷却速度2〜100℃/Sが得られるように
設計されている。The feature of this system is that it uses an air cooling method for cooling rates below 10℃/S, and an immersion method for cooling rates higher than that.The equipment has a two-line structure (upper and lower), and the immersion line uses fluidized stirring for cooling. It has a refrigerant circulation system etc. for this purpose. Furthermore, the air cooling line is equipped with a heat insulating cover and a blower, and is designed to obtain a desired cooling rate of 2 to 100°C/S.
tΔI酊講tagコh+ ←ユしネ1■晶ノ;1しか
し、ばね鋼や高炭素鋼線材の調整冷却とりわけばね鋼に
おいては、沸点近傍の熱水で浸漬冷却すれば、冷却速度
が速すぎて適冷組織を発生するし、単なる大気の自然放
冷であれば冷却速度の不均一を生じ、冷却速度の遅くな
る部位でフェライト脱炭を発生する問題を生じる。この
ことから、熱水での浸漬冷却と大気での自然放冷の中間
の冷却速度を得る手段として一般的に風をかける冷却方
式がとられている。しかし、レーイングヘッドでコイリ
ングされ、連続的に非同心円状の線材リングが、コンベ
アに乗せられて冷却される時の各リングの重なり程度は
、リング中心から両側部にわたって変化するので、衝風
量をリングの重なり程度に応じて変化させる等の対策を
講じている。しかし、リングの重なり部は下方から風を
かける従来法では不十分で均一冷却は難しく、lリング
内の冷却速度バラツキは熱水での浸漬冷却処理材に比べ
て大きくなる。従って、引張り強さ等の機械的性質のバ
ラツキが大きくなり、二次加工蒔の工具摩耗1寸法精度
に悪″#饗をおよぼすほか矯直時の曲り発生の原因にも
なる等の問題がある。tΔI Drunk Course tag koh+ ←Yushine 1 ■ Crystal; 1 However, the cooling rate is too fast for adjusting cooling of spring steel and high carbon steel wire, especially for spring steel, if immersed in hot water near the boiling point. However, if the material is simply allowed to cool naturally in the atmosphere, the cooling rate will be non-uniform, causing the problem of ferrite decarburization occurring in areas where the cooling rate is slow. For this reason, a cooling method in which air is applied is generally used as a means of achieving a cooling rate intermediate between immersion cooling in hot water and natural cooling in the atmosphere. However, when the continuous non-concentric wire rings are coiled in a laying head and cooled on a conveyor, the degree of overlapping of each ring changes from the center of the ring to both sides, so the amount of air blast is Measures are taken such as changing the amount depending on the degree of ring overlap. However, the conventional method of applying air from below to the overlapping portions of the rings is insufficient and uniform cooling is difficult, and the variation in the cooling rate within the ring is greater than in materials immersed in hot water. Therefore, variations in mechanical properties such as tensile strength become large, causing problems such as tool wear during secondary machining, which impairs dimensional accuracy and also causes bending during straightening. .
また、均質パテンティングのための冷却方法として、気
体と温水との強攪拌状態の流体冷媒中での浸漬冷却法が
あるが、冷媒が強攪拌状態にあるので5.51■φ付近
の細径線材はコンベアに乗せられて過材されろ過程で揺
動を起し、搬送時のトラブルを引起したり、部分的にス
ケール剥離を起し、二次加工前のメカニカルデスケーリ
ングや酸洗時の肌荒れの原因となるほか、多量の空気を
吹込むため、ブロワ−等のランニングコストおよびそれ
らの冷媒循環装置を必要とし、設備の大型化、複雑化に
つながるほか、設備コストも非常に高くなる問題があっ
た。In addition, as a cooling method for homogeneous patenting, there is an immersion cooling method in a strongly agitated fluid refrigerant of gas and hot water. Wire rods are placed on a conveyor and shake during the overloading process, causing trouble during conveyance, partial peeling of scale, and mechanical descaling before secondary processing and during pickling. In addition to causing rough skin, blowing in a large amount of air requires running costs such as blowers and refrigerant circulation equipment, which leads to larger and more complex equipment, and extremely high equipment costs. was there.
(問題点を解決するための手段)
本発明は上記欠点を改善するための全く新しい冷却方法
を提供するものである。すなわち、風冷の範囲と冷媒を
強撹拌状態で浸漬冷却する範囲の冷却状態を、水に発泡
剤を添加して得られる含水量0.01 g〜80 g
/10h+の泡に浸漬することにより得るもので、これ
によって安定な状態で鋼材冷却を行う方法を提供するも
のであり、更にその泡を界面活性剤や水溶性ポリマーか
ら作ることで、所望の冷却速度はもとより、冷却速度の
バラツキも他冷却方法に比べ改善するものである。(Means for Solving the Problems) The present invention provides a completely new cooling method for improving the above-mentioned drawbacks. In other words, the cooling state is between the range of air cooling and the range of immersion cooling with strong stirring of the refrigerant, and the water content obtained by adding a foaming agent to water is 0.01 g to 80 g.
/10h+ foam, which provides a method for cooling steel in a stable state.Furthermore, by making the foam from a surfactant or water-soluble polymer, the desired cooling can be achieved. This method improves not only the speed but also the variation in cooling rate compared to other cooling methods.
以下、本発明について図面にもとづいて詳細に説明する
。Hereinafter, the present invention will be explained in detail based on the drawings.
第1図に示す設備においては、冷却槽lの底部側内部に
、細孔3を多数設けた床板4を設置し、該床板4と冷却
槽1の底板2との間に、界面活性剤や水溶性ポリマーを
含む水溶液5を貯留し、その中にフィルター6を浸漬し
ている。In the equipment shown in FIG. 1, a floor plate 4 with a large number of pores 3 is installed inside the bottom side of the cooling tank l, and between the floor plate 4 and the bottom plate 2 of the cooling tank 1, a surfactant or a An aqueous solution 5 containing a water-soluble polymer is stored, and a filter 6 is immersed therein.
このフィルター6に気体(空気)を吹き込むことにより
、水溶液5は発泡し、床板4の細孔3から冷却槽1内に
泡8が吹出し、槽内は泡で充満する。この泡中に線材7
を浸漬して冷却することで次の結果を得た。By blowing gas (air) into this filter 6, the aqueous solution 5 is foamed, and bubbles 8 are blown out from the pores 3 of the floor plate 4 into the cooling tank 1, and the tank is filled with bubbles. In this bubble, wire rod 7
The following results were obtained by immersing and cooling.
すなわち、常温の水lfLに陰イオン界面活性剤0.5
wtlと高級アルコール0.OEi wt$を添加し
た水込んで発生させた泡に、0.4zのCを含有する直
径9.5 amφの線材を800℃に加熱して浸漬冷却
し、その冷却速度を測定した。その結果、第2図に示す
とおり泡中の水分量が増すにしたがって冷却速度は増加
する。また1発泡剤(界面活性剤や水溶性ポリマー)を
含む水溶液温度の低い程、冷却速度は増加することがわ
かる(図中、・印の実線は40℃、Δ印の破線は95℃
の水溶液温度)、このような効果は、泡中水分の蒸発潜
熱による冷却と沸凰伝熱さらには放射伝熱の組合せによ
るものと考えられる。That is, 0.5 liters of anionic surfactant is added to 1fL of water at room temperature.
wtl and higher alcohol 0. A wire rod with a diameter of 9.5 amφ containing 0.4z C was heated to 800° C. and cooled by immersion in foam generated by pouring water into which OEi wt$ was added, and the cooling rate was measured. As a result, as shown in FIG. 2, as the amount of water in the bubbles increases, the cooling rate increases. It can also be seen that the lower the temperature of the aqueous solution containing the blowing agent (surfactant or water-soluble polymer), the higher the cooling rate (in the figure, the solid line marked with . is 40°C, and the dashed line marked with Δ is 95°C).
(aqueous solution temperature), such an effect is thought to be due to a combination of cooling due to the latent heat of vaporization of water in the bubbles, boiling heat transfer, and further radiation heat transfer.
したがって、泡中の水分量や発泡剤を含む水溶液の温度
を調整することで、冷却速度を自在に制御することがで
き、線材の抗張力等の機械的性質のコントロールが可能
となる。Therefore, by adjusting the water content in the foam and the temperature of the aqueous solution containing the foaming agent, the cooling rate can be freely controlled, and the mechanical properties such as the tensile strength of the wire can be controlled.
本発明において、泡中の下限含水量0.01g /10
0■Iとしたのは、泡の中に高温線材を浸漬して連続冷
却できる限界の水分量である。いいかえれば、泡中水分
量が0.01 g /100m1未満になると、冷却速
1fI:ご互斗スゼiし1イ小力11清(L苓シlνか
/かス査分量である。また、発泡剤を含む水溶液の温度
を常温以下まで低下せしめて泡を生成させ、その泡で冷
却した時に得られる冷却速度が丁度従来の風で冷却して
得られる冷却速度をクリアーする水分量である。また、
上限80g/100m1は従来の多機能システムにおい
て、強撹拌状態の冷媒に浸漬して得られる冷却速度lθ
〜30℃/secをクリアーするのに必要な含水量に若
干の余裕をもって選んだ水分量である。ここで、泡中の
水分量は、発泡剤の種類や濃度1発泡剤を含む水溶液表
面から被冷却材までの距離、更には泡高や送気量、フィ
ルターの種類等によってコントロールされる。In the present invention, the lower limit water content in foam is 0.01g/10
0■I is the limit water content that allows continuous cooling of a high-temperature wire rod by immersing it in foam. In other words, when the water content in the foam is less than 0.01 g/100ml, the cooling rate is 1fI: 100g/100ml. , the temperature of an aqueous solution containing a blowing agent is lowered to below room temperature to generate bubbles, and the cooling rate obtained when cooling with the bubbles is exactly the amount of water that exceeds the cooling rate obtained by cooling with conventional wind. .Also,
The upper limit of 80 g/100 m1 is the cooling rate lθ obtained by immersion in a strongly agitated refrigerant in a conventional multifunctional system.
The water content was selected with a slight margin to the water content required to clear the temperature of ~30°C/sec. Here, the amount of water in the foam is controlled by the type of foaming agent, the distance from the surface of the aqueous solution containing the foaming agent at a concentration of 1 to the material to be cooled, the height of the foam, the amount of air supplied, the type of filter, etc.
線材冷却に使用する泡は界面活性剤や水溶性ポリマーか
らつくることで、安定的に連続冷却が可能である。すな
わち、泡の耐熱性9粒子径、含水量等のコントロールが
容易にできるほか、冷却速度のバラツキは熱水での浸漬
冷却より改良される。これは発泡剤として、界面活性剤
や水溶性ポリマーでつくられる泡は、線材リング重なり
密度の高い部位でも、泡がコイル周囲を完全に包囲して
いるので、線材の放散熱量に対応して泡中水分の蒸発速
度が変化するためである。すなわち、線材リングの重な
り密度の高い所は、泡中水分の蒸発速度が早くなり抜熱
量が多くなる。それでも泡が消滅しないのは、泡生成速
度が十分それを補っているためと考えられる。The foam used to cool the wire is made from surfactants and water-soluble polymers, allowing stable and continuous cooling. That is, it is possible to easily control the particle size, water content, etc. of the foam, and the variation in cooling rate is improved compared to immersion cooling in hot water. As a foaming agent, the foam made from surfactants and water-soluble polymers completely surrounds the coil even in areas where wire rings overlap and have a high density, so the foam responds to the amount of heat dissipated by the wire. This is because the evaporation rate of water inside changes. That is, in areas where the wire rings have a high overlap density, the evaporation rate of water in the bubbles becomes faster and the amount of heat removed increases. The reason why the bubbles still did not disappear is thought to be because the bubble generation rate sufficiently compensated for this.
次に、界面活性剤及び水溶性ポリマーの必要性について
説明する。Next, the necessity of surfactants and water-soluble polymers will be explained.
これは、発泡剤として界面活性剤を使用すると、界面活
性剤が気液表面に吸着し1表面張力を低下させると共に
表面粘度を増加させ、泡形成時の発泡性、泡径の大小あ
るいは均一性、安定性等を改善し、又、水溶性ポリマー
を使用すると、これらが主に気液表面の表面粘性あるい
は表面粘弾性を向上させ、安定な泡を形成することによ
るものである。This is because when a surfactant is used as a foaming agent, the surfactant adsorbs onto the surface of the gas and liquid, lowering the surface tension and increasing the surface viscosity. , stability, etc., and when water-soluble polymers are used, they mainly improve the surface viscosity or surface viscoelasticity of the gas-liquid surface and form stable bubbles.
このように、界面活性剤や水溶性ポリマーを起泡剤とし
て使用すると、生成した泡が均一化、安定化し、含水量
が0.01〜80g/100m1の均一な泡の層を任意
に作ることが出来る。この泡を高温線材の冷却に用いる
と、冷却雰囲気が制御しやすくなり、品質振れ、ロフト
振れの少ない、目標とする品質の線材を安定に製造する
ことが出来る。In this way, when a surfactant or a water-soluble polymer is used as a foaming agent, the generated foam becomes uniform and stabilized, and a uniform layer of foam with a water content of 0.01 to 80 g/100 m1 can be arbitrarily created. I can do it. When this foam is used to cool high-temperature wire rods, the cooling atmosphere can be easily controlled, making it possible to stably produce wire rods of targeted quality with less quality fluctuations and loft fluctuations.
一方、これら発泡剤を使用せず強制攬はん等の機械力の
みにより泡を形成させる方法も考えられるが、このよう
にして形成された泡は表面エネルギーが高く、表面粘性
も低い為、泡も不均一で、安定性が悪い、このため、線
材の冷却雰囲気は一定せず、ロフト振れ、品質の振れが
生じ、目標とする品質の線材を安定に製造することは困
難である。On the other hand, it is also possible to form foam using only mechanical force such as forced extraction without using these foaming agents, but the foam formed in this way has high surface energy and low surface viscosity. As a result, the cooling atmosphere for the wire is not constant, resulting in loft fluctuations and quality fluctuations, making it difficult to stably produce wire rods of the desired quality.
本発明に於いて用いられる発泡剤は界面活性剤及び水溶
性ポリマーであるが、それらについて以下に詳しく述べ
る。The blowing agents used in the present invention are surfactants and water-soluble polymers, which will be described in detail below.
ここに言う界面活性剤とは、気液表面に吸着して表面活
性を低下させる水可溶性の有機系化合物のことであり、
より具体的には、脂肋酩塩類、高級アルコール硫酸エス
テル塩類、液体脂肪油硫酸エステル塩類、脂肪族アミン
および脂肪族アマイ類、二塩基性脂肪酸エステルのスル
ホン塩類、脂肪酸アミドスルホン酸塩類、アルキルアリ
ルスルホン醜塩類、ホルマリン縮合のナフタリンスルポ
ン酸塩類9等の7ニオン活性剤、又脂肪族アミン塩類、
第4級アンモニウム塩類、アルキルピリジニウム塩類等
のカチオン系活性剤、又、ポリオキシエチレンアルキル
エーテル類、ポリオキシエチレンアルキルフェノールエ
ーテル類、ポリオキシエチレンアルキルエステル類、ソ
ルビタンアキルエステル類ポリオキシソルビタンアルキ
ルエステル類1等の非イオン系活性剤、あるいはアルキ
ルベタイン、アルキルジメチルアミンオキサイド。The surfactant referred to here is a water-soluble organic compound that adsorbs to the surface of gas and liquid and reduces surface activity.
More specifically, fatty acid salts, higher alcohol sulfate ester salts, liquid fatty oil sulfate ester salts, aliphatic amines and aliphatic flaxes, sulfone salts of dibasic fatty acid esters, fatty acid amide sulfonates, and alkylaryls. 7-ion activators such as sulfone ugly salts, formalin-condensed naphthalene sulfonic acid salts 9, and aliphatic amine salts,
Cationic activators such as quaternary ammonium salts, alkylpyridinium salts, polyoxyethylene alkyl ethers, polyoxyethylene alkylphenol ethers, polyoxyethylene alkyl esters, sorbitan alkyl esters, polyoxysorbitan alkyl esters 1 nonionic surfactants such as alkyl betaines, alkyl dimethylamine oxides, etc.
アルキルアラニン等の両性活性剤等が主だった物として
上げられるがこれに限定されるものではない。Main examples include amphoteric active agents such as alkylalanine, but are not limited thereto.
泡生成に際しては、これら界面活性剤の1種あるいは2
種以上の混合物を木に対しo、oot〜40%になるよ
う加え使用することが好ましい。When generating foam, one or both of these surfactants are used.
It is preferable to use a mixture of more than one species by adding it to the tree in an amount of o, oot to 40%.
又、水溶性ポリマーとしては天然9合成、半合スターチ
、デンプン類、ふのり、寒天、アルギン酸ソーダ、アラ
ビアゴム、トラガントゴム、トロロアロイ、こんに◆く
、にかわ、カゼイン、ゼラチン、卵白、血しょうタンパ
ク、プルラン、デキストリン、カルボキシデンプン、プ
リテシュゴム、ヂアルデヒドデンプン、カチオンデンプ
ン。In addition, water-soluble polymers include natural 9 synthetics, half-combined starch, starches, funori, agar, sodium alginate, gum arabic, gum tragacanth, trolo alloy, konjac, glue, casein, gelatin, egg white, plasma protein, pullulan. , dextrin, carboxy starch, pritesh gum, dialdehyde starch, cationic starch.
ビスコース、メチルセルロース、エチルセルロース、カ
ルボキシメチルセルロース
チルセルロース、ポリビニルアルコール、ポリエチレン
グリコール、ポリアルキレングリコール。Viscose, methylcellulose, ethylcellulose, carboxymethylcellulose, methylcellulose, polyvinyl alcohol, polyethylene glycol, polyalkylene glycol.
ポリアクリルアミド、ポリアクリル酸,ポリビニルピロ
リドン、水よう性アルキッドポリビニルエーテル、ポリ
マレイン酸共重合体,ポリエチレンイミン、サポニン等
が主だった物として上げられるがこれに限定されるもの
ではない。Main examples include polyacrylamide, polyacrylic acid, polyvinylpyrrolidone, aqueous alkyd polyvinyl ether, polymaleic acid copolymer, polyethyleneimine, saponin, etc., but are not limited thereto.
泡生成に際しては、これら水溶性ポリマーの1種あるい
は2種以上を水に対し0.01〜3ozに成るよう加え
使用することが好ましい。When generating foam, it is preferable to use one or more of these water-soluble polymers in an amount of 0.01 to 3 oz to water.
以」二述べた界面活性剤と水溶性ポリマーは任意の割合
で混合して使用してもよい.又泡の性状や安定性を改善
するため、界面活性剤水溶液あるいは界面活性剤と水溶
性ポリマーの混合液に適量のキレート剤,ビルダー、高
級アルコール等を加えてもよい。The surfactants and water-soluble polymers mentioned below may be mixed in any proportion. Further, in order to improve the properties and stability of the foam, an appropriate amount of a chelating agent, builder, higher alcohol, etc. may be added to the aqueous surfactant solution or the mixture of the surfactant and water-soluble polymer.
キレート剤としては例えばジヒドロキシエチルグリシン
、ヒドロキシエチルイミノ2酢酸,ニトリロ3酢酸,ヒ
ドロキシエチルエチレンジアミン3酢酸,エチレンジア
ミンテトラ酢酸,ジエチレントリアミン5酢酸,等のア
ミノカルボン酸塩。Examples of chelating agents include aminocarboxylate salts such as dihydroxyethylglycine, hydroxyethyliminodiacetic acid, nitrilotriacetic acid, hydroxyethylethylenediaminetriacetic acid, ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, and the like.
クエン酸ソーダ、グルコン酸ソーダ、酒石酸ソーダ、等
のオキシカルボン酸,ポリカルボン酸,ヒドロキシエタ
ンジホスホン酸,ニトリロトリスメチレンホスホン酸,
エチレンジアミンテトラメチレンホン酸,等のホスホン
酸類あるいはトリポリリン酸ソーダ、ビロリン酸ソーダ
等の縮合リン酸塩等が有り、1種又は2種以上を0.0
01〜20%使用するのが好ましい。Oxycarboxylic acids such as sodium citrate, sodium gluconate, and sodium tartrate, polycarboxylic acids, hydroxyethane diphosphonic acid, nitrilotrismethylenephosphonic acid,
There are phosphonic acids such as ethylenediaminetetramethylenephonic acid, condensed phosphates such as sodium tripolyphosphate, sodium birophosphate, etc., and one or more of them can be used at 0.0
It is preferable to use 0.01 to 20%.
又、高級アルコールは炭素数が6〜36の1級及び2級
のアルコールが好ましく、ヘキサノール。Further, the higher alcohol is preferably a primary or secondary alcohol having 6 to 36 carbon atoms, and hexanol.
オクタツール、ラウリルアルコール、ミリスチルアルコ
ール、セチルアルコール、ステアリルアルコール、オレ
イルアルコール、炭素数が18.24.38等のゲルベ
アルコール等の1種又は2種以−Lを界面活性剤に対し
0.5〜30%加えてもよい。One or more types of octatool, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, Guerbet alcohol with a carbon number of 18,24,38, etc., are added to the surfactant in an amount of 0.5 to 100%. You may add 30%.
その他、ビルダー例えば珪酸ソーダ、硫酸ソーダ、炭酸
ソーダ等を上記配合物に対し0.1〜30%加えてもよ
い。In addition, builders such as sodium silicate, sodium sulfate, and soda carbonate may be added in an amount of 0.1 to 30% to the above formulation.
(実施例)
次に第1図の冷却装置で冷却した時の実施例について詳
しく説明する。(Example) Next, an example in which cooling is performed using the cooling device shown in FIG. 1 will be described in detail.
冷却槽1の床板4と底板2との間に陰イオン界面剤0.
5 wt$と高級アルコール0.06 wt$添加した
約95℃の水溶液5を貯留し、その中に約1〜5pLの
フィルター6が浸漬しである.このフィルター6に7
fl /winの空気を送り、冷却槽内を粒径1〜3■
程度の泡8で高さ約250■まで充満させる。Between the floor plate 4 and the bottom plate 2 of the cooling tank 1, an anionic surfactant 0.
An aqueous solution 5 at about 95° C. to which $5 wt. This filter 6 to 7
Send fl/win air to reduce particle size from 1 to 3cm inside the cooling tank.
Fill to a height of about 250cm with bubbles of 8 degrees.
かかる準備が整った後、約900℃に加熱した9.5■
φの線材の束7を浸漬冷却した.ここで、冷却速度のバ
ラツキを小さくするため、線材の東が常うに、発泡剤を
含む水溶液の表面から線材までの距離を約50i+st
に調整すると共に、泡が完全に高温線材を浸漬した状態
に保つためにフィルターに送る空気も一定量連続的に送
った。After this preparation was completed, 9.5■ heated to about 900℃
A bundle 7 of φ wire rods was immersed and cooled. Here, in order to reduce the variation in cooling rate, the distance from the surface of the aqueous solution containing the foaming agent to the wire is approximately 50i + st.
At the same time, a certain amount of air was continuously sent to the filter to keep the high-temperature wire completely immersed in the bubbles.
その結果、本発明の泡で冷却することにより第3図に示
す■の冷却曲線となり、熱水での浸漬冷却で得る■の冷
却曲線と大気での自然放冷で得る■の冷却曲線の中間に
容易にコントロールできる。As a result, cooling with the foam of the present invention results in a cooling curve (■) shown in Figure 3, which is between the cooling curve (■) obtained by immersion cooling in hot water and the cooling curve (■) obtained by natural cooling in the atmosphere. can be easily controlled.
また、以上の説明において、吹き込む気体は一般に空気
を使用するが、冷却線材の表面酸化防止の観点からN2
ガス等の不活性ガスあるいは還元性ガスも使用できる.
また、本実験では一定の径の穴を有するフィルターに空
気を送入するいわゆる送気法により泡を生成させたが、
他に攪拌法。In the above explanation, air is generally used as the gas to be blown in, but from the viewpoint of preventing surface oxidation of the cooling wire, N2
Inert gases such as gases or reducing gases can also be used.
In addition, in this experiment, bubbles were generated using the so-called air supply method, in which air is introduced into a filter with holes of a certain diameter.
Another method is stirring.
振とう法.沸騰法,減圧法,溶解度減少法あるいはそれ
らを組合せた方法があり、本発明は泡の生成方法を限定
するものでない。又、冷却槽の外で所望の泡を生成した
後、冷却槽に送入することも通常1発泡剤を含む水溶液
の温度はO℃〜100℃の間までで使用されるが、常温
で使用して泡中の水分量をコントロールして所望の冷却
速度を得る方法が省エネルギー上望ましい、また、吹込
気体の温度も予熱して使用することも可能である。Shaking method. There are boiling methods, depressurization methods, solubility reduction methods, or a combination thereof, and the present invention does not limit the foam generation method. In addition, it is also possible to generate the desired foam outside the cooling tank and then feed it into the cooling tank.1 Usually, the temperature of the aqueous solution containing the foaming agent is between 0°C and 100°C, but it can be used at room temperature. A method of controlling the amount of water in the foam to obtain a desired cooling rate is desirable from the viewpoint of energy saving, and it is also possible to preheat the temperature of the blown gas before use.
(発明の効果)
以−ヒ、詳しく説明したように1本発明は線材を冷却す
るための泡の水分量や温度を制御して冷却速度をコント
ロールする冷却方法で、従来の風をかけて冷却する方法
に比べて均一冷却が可能である。また、強攪拌状態の温
液体に浸漬して冷却する方法に比べて、適材抵抗が小さ
く5.5■厘φのような細径線材であっても適材性は良
好であり、さらにスケールの剥離もなく、酸洗による肌
荒れ等の問題もない、更に、本発明は冷媒処理や排蒸設
備、冷媒循環装置等を必要とせず、構造筒中で設備費も
非常に安価である。(Effects of the Invention) As explained in detail below, the present invention is a cooling method that controls the cooling rate by controlling the moisture content and temperature of bubbles for cooling the wire, which is different from the conventional method of cooling by blowing air. Uniform cooling is possible compared to other methods. In addition, compared to the method of cooling by immersing in hot liquid under strong agitation, the suitable material resistance is smaller, and the material properties are good even with a small diameter wire material such as 5.5 cmφ, and the peeling of scale is also possible. Furthermore, the present invention does not require refrigerant treatment, evaporation equipment, refrigerant circulation equipment, etc., and the equipment cost in the structural cylinder is very low.
第1図は本発明を実施するための設備例を示す断面図で
あり、第2図、第3図は本発明方法によって熱処理した
時の冷却速度と冷却曲線を示すグラフである・
1・・・冷却槽、2・・・底板、3・・・細孔、4・・
・床板、5・・・水溶液、6・・・フィルター、7・・
・線材の束、8・・・泡。Figure 1 is a sectional view showing an example of equipment for carrying out the present invention, and Figures 2 and 3 are graphs showing the cooling rate and cooling curve when heat treated by the method of the present invention.・Cooling tank, 2...bottom plate, 3...pores, 4...
・Floor plate, 5...aqueous solution, 6...filter, 7...
・Bundle of wire rod, 8... bubble.
Claims (2)
g〜80g/100mlの泡の中に高温線材を浸漬し冷
却することを特徴とする圧延線材の熱処理方法。(1) Water content 0.01 obtained by adding a foaming agent to water
A heat treatment method for a rolled wire rod, which comprises immersing a high-temperature wire rod in bubbles of g to 80 g/100 ml and cooling it.
くられることを特徴とする特許請求の範囲第1項記載の
圧延線材の熱処理方法。(2) The method for heat treatment of rolled wire rod according to claim 1, characterized in that the blowing agent is made from a surfactant or a water-soluble polymer.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20671686A JPS6362824A (en) | 1986-09-04 | 1986-09-04 | Heat treatment of rolled wire rod |
US07/210,581 US4931108A (en) | 1986-09-04 | 1987-09-04 | Method of heat treatment of rolled steel material using foams impregnated with water soluble polymers |
PCT/JP1987/000660 WO1988001652A1 (en) | 1986-09-04 | 1987-09-04 | Process for heat-treating rolled steel product |
DE19873790510 DE3790510T (en) | 1986-09-04 | 1987-09-04 | |
DE3790510A DE3790510C2 (en) | 1986-09-04 | 1987-09-04 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20671686A JPS6362824A (en) | 1986-09-04 | 1986-09-04 | Heat treatment of rolled wire rod |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6362824A true JPS6362824A (en) | 1988-03-19 |
JPH0450370B2 JPH0450370B2 (en) | 1992-08-14 |
Family
ID=16527925
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20671686A Granted JPS6362824A (en) | 1986-09-04 | 1986-09-04 | Heat treatment of rolled wire rod |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6362824A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6442520A (en) * | 1987-08-07 | 1989-02-14 | Sumitomo Metal Ind | Method for cooling metal |
JPH01123031A (en) * | 1987-11-06 | 1989-05-16 | Nippon Steel Corp | Method for heat-treatment of machine structural members |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50104718A (en) * | 1974-01-28 | 1975-08-19 | ||
JPS57140834A (en) * | 1981-02-25 | 1982-08-31 | Sumitomo Electric Ind Ltd | Method and device for direct heat treatment of steel wire rod |
JPS57143440A (en) * | 1981-02-28 | 1982-09-04 | Sumitomo Electric Ind Ltd | Heat treatment of steel wire rod |
JPS60248824A (en) * | 1984-05-24 | 1985-12-09 | Sumitomo Electric Ind Ltd | Method and device for direct heat treatment of middle and high carbon steel wire rod |
JPS61526A (en) * | 1984-06-13 | 1986-01-06 | Sumitomo Electric Ind Ltd | Method and apparatus for heat treating metal or the like |
-
1986
- 1986-09-04 JP JP20671686A patent/JPS6362824A/en active Granted
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50104718A (en) * | 1974-01-28 | 1975-08-19 | ||
JPS57140834A (en) * | 1981-02-25 | 1982-08-31 | Sumitomo Electric Ind Ltd | Method and device for direct heat treatment of steel wire rod |
JPS57143440A (en) * | 1981-02-28 | 1982-09-04 | Sumitomo Electric Ind Ltd | Heat treatment of steel wire rod |
JPS60248824A (en) * | 1984-05-24 | 1985-12-09 | Sumitomo Electric Ind Ltd | Method and device for direct heat treatment of middle and high carbon steel wire rod |
JPS61526A (en) * | 1984-06-13 | 1986-01-06 | Sumitomo Electric Ind Ltd | Method and apparatus for heat treating metal or the like |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6442520A (en) * | 1987-08-07 | 1989-02-14 | Sumitomo Metal Ind | Method for cooling metal |
JPH01123031A (en) * | 1987-11-06 | 1989-05-16 | Nippon Steel Corp | Method for heat-treatment of machine structural members |
Also Published As
Publication number | Publication date |
---|---|
JPH0450370B2 (en) | 1992-08-14 |
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