JPH0192388A - Corrosion inhibitor - Google Patents
Corrosion inhibitorInfo
- Publication number
- JPH0192388A JPH0192388A JP25050287A JP25050287A JPH0192388A JP H0192388 A JPH0192388 A JP H0192388A JP 25050287 A JP25050287 A JP 25050287A JP 25050287 A JP25050287 A JP 25050287A JP H0192388 A JPH0192388 A JP H0192388A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- corrosion inhibitor
- iron
- corrosion
- inhibitor
- 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
- 239000003112 inhibitor Substances 0.000 title claims abstract description 21
- 238000005260 corrosion Methods 0.000 title claims abstract description 15
- 230000007797 corrosion Effects 0.000 title claims abstract description 15
- 239000002184 metal Substances 0.000 claims abstract description 9
- 229910052751 metal Inorganic materials 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- -1 ferrous metals Chemical class 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 23
- 229910052742 iron Inorganic materials 0.000 abstract description 9
- 238000004090 dissolution Methods 0.000 abstract description 6
- 150000002739 metals Chemical class 0.000 abstract description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 3
- 230000002378 acidificating effect Effects 0.000 abstract description 2
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 abstract 1
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 abstract 1
- JWZXKXIUSSIAMR-UHFFFAOYSA-N methylene bis(thiocyanate) Chemical compound N#CSCSC#N JWZXKXIUSSIAMR-UHFFFAOYSA-N 0.000 abstract 1
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000010953 base metal Substances 0.000 description 4
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- VYHVQEYOFIYNJP-UHFFFAOYSA-N methyl thiocyanate Chemical compound CSC#N VYHVQEYOFIYNJP-UHFFFAOYSA-N 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- KFFQABQEJATQAT-UHFFFAOYSA-N N,N'-dibutylthiourea Chemical compound CCCCNC(=S)NCCCC KFFQABQEJATQAT-UHFFFAOYSA-N 0.000 description 2
- FLVIGYVXZHLUHP-UHFFFAOYSA-N N,N'-diethylthiourea Chemical compound CCNC(=S)NCC FLVIGYVXZHLUHP-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 2
- 235000011054 acetic acid Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- ABNDFSOIUFLJAH-UHFFFAOYSA-N benzyl thiocyanate Chemical compound N#CSCC1=CC=CC=C1 ABNDFSOIUFLJAH-UHFFFAOYSA-N 0.000 description 2
- UCGFRIAOVLXVKL-UHFFFAOYSA-N benzylthiourea Chemical compound NC(=S)NCC1=CC=CC=C1 UCGFRIAOVLXVKL-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000005554 pickling Methods 0.000 description 2
- 229910052717 sulfur Chemical group 0.000 description 2
- 239000011593 sulfur Chemical group 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- GAWAYYRQGQZKCR-REOHCLBHSA-N (S)-2-chloropropanoic acid Chemical compound C[C@H](Cl)C(O)=O GAWAYYRQGQZKCR-REOHCLBHSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- LILPOSVDSDEBCD-UHFFFAOYSA-N 2-thiocyanatoethyl thiocyanate Chemical compound N#CSCCSC#N LILPOSVDSDEBCD-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- SDOXAONWZOPJRB-UHFFFAOYSA-N 4-thiocyanatobutyl thiocyanate Chemical compound N#CSCCCCSC#N SDOXAONWZOPJRB-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 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
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
- FCSHMCFRCYZTRQ-UHFFFAOYSA-N N,N'-diphenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1=CC=CC=C1 FCSHMCFRCYZTRQ-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229960004275 glycolic acid Drugs 0.000 description 1
- 229910052595 hematite Inorganic materials 0.000 description 1
- 239000011019 hematite Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
- C23G1/02—Cleaning or pickling metallic material with solutions or molten salts with acid solutions
- C23G1/04—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors
- C23G1/06—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors
- C23G1/065—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors sulfur-containing compounds
Abstract
Description
【発明の詳細な説明】
イ)産業上の利用分野
本発明は鉄系金属の腐食抑制剤に関するものであり、更
に詳しくは一般式
[式中mは0〜5.nは2〜3である]で示される化合
物による、酸性下における鉄系金属の腐食抑制剤に関す
るものである。DETAILED DESCRIPTION OF THE INVENTION A) Industrial Application Field The present invention relates to a corrosion inhibitor for iron-based metals. The present invention relates to a corrosion inhibitor for iron-based metals under acidic conditions using a compound represented by the following formula: n is 2 to 3.
口)従来技術
従来、鉄系金属の酸処理には、鉄やステンレス鋼の製造
時に行われる酸洗いや化学プラント、火力発電用大型ボ
イラー、各種熱交換器等の化学洗浄などが挙げられ、い
ずれも金属に付着したスケールを除去することを目的と
して行われている。使用される酸も、使用場面によって
各種各様で、例えば無機酸としては、塩酸、硫酸、燐酸
、弗酸、スルファミン酸等があり、有機酸としては、酢
酸、クエン酸、乳酸、シュウ酸、コハク酸、酒石酸、ギ
酸、ヒドロキシ酢酸、モノクロル酢酸、リンゴ酸、チオ
リンゴ酸、プロピオン酸、チオグリコール酸、クロルプ
ロピオン酸、エチレンジアミン四酢酸等が挙げられる。Conventional technology Conventionally, acid treatment of ferrous metals includes pickling during the production of iron and stainless steel, chemical cleaning of chemical plants, large boilers for thermal power generation, various heat exchangers, etc. It is also used for the purpose of removing scale attached to metal. The acids used vary depending on the usage situation; for example, inorganic acids include hydrochloric acid, sulfuric acid, phosphoric acid, hydrofluoric acid, sulfamic acid, etc., and organic acids include acetic acid, citric acid, lactic acid, oxalic acid, Examples include succinic acid, tartaric acid, formic acid, hydroxyacetic acid, monochloroacetic acid, malic acid, thiomalic acid, propionic acid, thioglycolic acid, chloropropionic acid, and ethylenediaminetetraacetic acid.
これらの酸による脱スケールは、スケールのみを溶解さ
せるかまたは、スケールを剥離させ、素地金属の溶解を
最小限にすることが理想でこのために通常、腐食抑制剤
(以下インヒビターと称す)・が添加されている。熱処
理した鉄の表面には、a Fe2O3<へマタイト)
やFe5C)s(マグネタイト)やFed(ビスタイト
)といった鉄酸化物が形成されるため、通常10〜15
%塩酸下40〜50℃でスケールの溶解除去が行われて
いる。In descaling using these acids, it is ideal to dissolve only the scale or peel off the scale and minimize the dissolution of the base metal, and for this purpose, corrosion inhibitors (hereinafter referred to as inhibitors) are usually used. has been added. On the surface of heat-treated iron, a Fe2O3<hematite)
Since iron oxides such as , Fe5C)s (magnetite) and Fed (bistite) are formed, it is usually 10 to 15
Dissolution and removal of scale is carried out at 40-50°C under % hydrochloric acid.
この際、素地金属の溶解を阻止するためにインヒビター
を酸液に対して0.1〜3%程度添加している。インヒ
ビターの抑制機構としては、有機化合物の窒素、酸素、
リン、イオウなどのへテロ原子が素地金属のみに吸着し
、スケールには、はとんど吸着しないことから、脱スケ
ールの速度に影響することなく素地金属の溶解を抑制す
ると考えられている。At this time, an inhibitor is added in an amount of about 0.1 to 3% to the acid solution in order to prevent dissolution of the base metal. The inhibition mechanism of the inhibitor is that of organic compounds such as nitrogen, oxygen,
Since heteroatoms such as phosphorus and sulfur are adsorbed only to the base metal, and are hardly adsorbed to scale, it is thought that they suppress the dissolution of the base metal without affecting the rate of descaling.
ハ)発明が解決しようとする問題点
現在使用されているインヒビターとしては、牛脂アミン
、ステアリルアミン、ラウリルアミン等のアルキルアミ
ン、ジエチルチオウレア、ジブチルチオウレア、ジフェ
ニルチオウレア、エチレンチオウレア等のチオウレア系
化合物、ベンゾチアゾール、2−メルカプトベンゾチア
ゾール等のチアゾール系化合物、エチレンオキサイドを
付加させたポリエチレングリコール型の界面活性剤など
が挙げられる。C) Problems to be Solved by the Invention Currently used inhibitors include alkyl amines such as tallow amine, stearyl amine and lauryl amine, thiourea compounds such as diethyl thiourea, dibutyl thiourea, diphenyl thiourea and ethylene thiourea, and benzyl thiourea. Examples include thiazole compounds such as thiazole and 2-mercaptobenzothiazole, and polyethylene glycol type surfactants to which ethylene oxide is added.
これら脱スケールの全体的な問題として、工程のスピー
ド化が挙げられ、この酸洗いにおいても80〜100℃
と高温処理が望まれており、インヒビター性能も、より
高度なものが要求されている。The overall problem with descaling is speeding up the process, and even in this pickling process, the temperature is 80 to 100°C.
High-temperature treatment is desired, and higher inhibitor performance is also required.
二)発明の構成
本発明者らは、鋭意研究の結果、ベンゼン環にチオシア
ナートを2〜3残基導入された化合物、またはアルキレ
ンチオシアナートを2〜3残基導入された化合物が、従
来のインヒビターでは、予想され得ない抑制効果を発揮
することを見出し、本発明に至った。本発明の化合物を
例示すると、0−フェニレンビス(メチルチオシアナー
ト)、m−フェニレンビス(メチルチオシアナート)、
p−フェニレンビス(メチルチオシアナート)、p−フ
ェニレンビス(1,2−エタンジイルチオシアナート)
、p−フェニレンビス(1,4−ブタンジイルチオシア
ナート)等があげられる。2) Structure of the Invention As a result of intensive research, the present inventors have discovered that a compound in which 2 to 3 residues of thiocyanate are introduced into the benzene ring, or a compound in which 2 to 3 residues of alkylene thiocyanate are introduced, is different from the conventional one. It was discovered that an inhibitor exhibits an unexpected suppressive effect, leading to the present invention. Examples of the compounds of the present invention include 0-phenylenebis(methylthiocyanate), m-phenylenebis(methylthiocyanate),
p-Phenylenebis(methylthiocyanate), p-phenylenebis(1,2-ethanediylthiocyanate)
, p-phenylenebis(1,4-butanediylthiocyanate), and the like.
ホ)作用
本発明の化合物は、酸液に対し、0.01〜50重量パ
ーセン1へ、好ましくは、0.05〜し重量パーセント
添加することにより、低温ではもちろんのこと、高温に
おいても安定に鉄系金属の素地溶解を抑制することがで
きるものである。e) Effect The compound of the present invention can be added stably not only at low temperatures but also at high temperatures by adding 0.01 to 50 weight percent, preferably 0.05 to 50 weight percent, to the acid solution. It is possible to suppress the dissolution of iron-based metals.
本発明のインヒビターは公知のインヒビターと併用して
も差し支えなく、可溶化または製剤化するための必要な
薬剤と混合して使用されることも、なんら差し支えない
。The inhibitor of the present invention may be used in combination with known inhibitors, or may be mixed with necessary drugs for solubilization or formulation.
へ)実施例 以下、実施例を挙げて、本発明の詳細な説明する。f) Example Hereinafter, the present invention will be explained in detail with reference to Examples.
テストピースとして鉄(SPCC)50X10X1mm
を使用し、耐水研磨紙#320で研磨後、アセトンで脱
脂、乾燥して使用する。Iron (SPCC) 50X10X1mm as test piece
After polishing with waterproof abrasive paper #320, degrease with acetone and dry before use.
試yl!、Wi、とじては最も広範に使用されている1
0%塩酸、10%硫酸、10%酢酸を使用し、80℃に
おいて所定濃度のインヒビター添加量で実施する。Try it! , Wi, is the most widely used 1
The test is carried out using 0% hydrochloric acid, 10% sulfuric acid, and 10% acetic acid at 80° C. with a predetermined concentration of inhibitor added.
なお、腐食を促進させるため、各酸液には、Fe”50
g/lを添加しておく。In addition, in order to accelerate corrosion, each acid solution contains Fe"50
Add g/l.
比較例としては、無添加、ジエチルチオウレア、ジブチ
ルチオウレア、ベンジルチオシアナート、市販のインヒ
ビター(イビット#700 :住友化学工業株式会社製
)を使用した。As a comparative example, additive-free, diethylthiourea, dibutylthiourea, benzylthiocyanate, and a commercially available inhibitor (IBIT #700, manufactured by Sumitomo Chemical Co., Ltd.) were used.
腐食抑制率(%)は下記式にて算出しな。Calculate the corrosion inhibition rate (%) using the formula below.
腐食抑制率(%)= (A−B)/AXI00A:イン
ヒビター無添加の際の腐食減量B:インヒビター添加時
の際の腐食減量1)10%塩f!!(Fe”50g/1
)2)10%硫a(Fe”50g/I)
3)10%酢1it(Fe”50g/I)ト)発明の効
果
以上の実施例、比較例からベンゼン環にチオシアナート
またはアルキレンチオシアナートを2ないし3残基導入
した化合物は、鉄系金属の腐食抑制剤として有用である
ことが判明した。Corrosion inhibition rate (%) = (A-B)/AXI00A: Corrosion loss when no inhibitor is added B: Corrosion loss when inhibitor is added 1) 10% salt f! ! (Fe”50g/1
) 2) 10% sulfur a (Fe"50g/I) 3) 10% vinegar 1it (Fe"50g/I) g) Effect of the invention From the above examples and comparative examples, thiocyanate or alkylene thiocyanate was added to the benzene ring. It has been found that compounds into which two or three residues have been introduced are useful as corrosion inhibitors for iron-based metals.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25050287A JPH0637709B2 (en) | 1987-10-02 | 1987-10-02 | Corrosion inhibitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25050287A JPH0637709B2 (en) | 1987-10-02 | 1987-10-02 | Corrosion inhibitor |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0192388A true JPH0192388A (en) | 1989-04-11 |
JPH0637709B2 JPH0637709B2 (en) | 1994-05-18 |
Family
ID=17208834
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25050287A Expired - Lifetime JPH0637709B2 (en) | 1987-10-02 | 1987-10-02 | Corrosion inhibitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0637709B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6050113B2 (en) * | 2010-06-30 | 2016-12-21 | Ykk株式会社 | Slide fastener and manufacturing method of slide fastener |
-
1987
- 1987-10-02 JP JP25050287A patent/JPH0637709B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0637709B2 (en) | 1994-05-18 |
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