KR20230125449A - Manufacturing Method of Eco-friendly Rust remover which has Volatile Corrosion Inhibiting function - Google Patents
Manufacturing Method of Eco-friendly Rust remover which has Volatile Corrosion Inhibiting function Download PDFInfo
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- KR20230125449A KR20230125449A KR1020220022086A KR20220022086A KR20230125449A KR 20230125449 A KR20230125449 A KR 20230125449A KR 1020220022086 A KR1020220022086 A KR 1020220022086A KR 20220022086 A KR20220022086 A KR 20220022086A KR 20230125449 A KR20230125449 A KR 20230125449A
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 title claims abstract description 91
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 238000005260 corrosion Methods 0.000 title description 10
- 230000007797 corrosion Effects 0.000 title description 7
- 230000002401 inhibitory effect Effects 0.000 title 1
- 229910052751 metal Inorganic materials 0.000 claims abstract description 33
- 239000002184 metal Substances 0.000 claims abstract description 33
- 238000002156 mixing Methods 0.000 claims abstract description 25
- 238000000034 method Methods 0.000 claims abstract description 23
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 39
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 20
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 15
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 15
- 229920000053 polysorbate 80 Polymers 0.000 claims description 13
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 12
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 12
- 239000001630 malic acid Substances 0.000 claims description 12
- 235000011090 malic acid Nutrition 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 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 claims description 11
- 239000000176 sodium gluconate Substances 0.000 claims description 11
- 229940005574 sodium gluconate Drugs 0.000 claims description 11
- 235000012207 sodium gluconate Nutrition 0.000 claims description 11
- BYKRNSHANADUFY-UHFFFAOYSA-M sodium octanoate Chemical compound [Na+].CCCCCCCC([O-])=O BYKRNSHANADUFY-UHFFFAOYSA-M 0.000 claims description 11
- 239000012153 distilled water Substances 0.000 claims description 10
- 229960005480 sodium caprylate Drugs 0.000 claims description 10
- 230000000694 effects Effects 0.000 claims description 6
- 239000003814 drug Substances 0.000 claims description 4
- 230000002265 prevention Effects 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 230000008569 process Effects 0.000 abstract description 7
- 239000000126 substance Substances 0.000 abstract description 6
- 230000008859 change Effects 0.000 abstract description 4
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- 239000000356 contaminant Substances 0.000 abstract description 4
- 235000013373 food additive Nutrition 0.000 abstract description 4
- 239000002778 food additive Substances 0.000 abstract description 4
- 150000007524 organic acids Chemical class 0.000 abstract description 4
- 239000003638 chemical reducing agent Substances 0.000 abstract description 3
- 238000002845 discoloration Methods 0.000 abstract description 3
- 235000021107 fermented food Nutrition 0.000 abstract description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- 239000004615 ingredient Substances 0.000 abstract 2
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 238000003756 stirring Methods 0.000 description 14
- 239000011259 mixed solution Substances 0.000 description 13
- 238000012360 testing method Methods 0.000 description 12
- 239000000203 mixture Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 7
- 239000000523 sample Substances 0.000 description 7
- 239000012488 sample solution Substances 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 6
- -1 ferrous metals Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 150000007522 mineralic acids Chemical class 0.000 description 3
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 3
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 3
- 229940068968 polysorbate 80 Drugs 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 229910000975 Carbon steel Inorganic materials 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 150000001565 benzotriazoles Chemical class 0.000 description 2
- 239000010962 carbon steel Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000013527 degreasing agent Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- IRGKJPHTQIWQTD-UHFFFAOYSA-N 2,7-dibromopyrene-1,3,6,8-tetrone Chemical compound O=C1C(Br)C(=O)C2=CC=C3C(=O)C(Br)C(=O)C4=CC=C1C2=C43 IRGKJPHTQIWQTD-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-N Gluconic acid Natural products OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 1
- 229920005479 Lucite® Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000013475 authorization Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Detergent Compositions (AREA)
Abstract
Description
본 발명은 생분해성 물질을 이용하여 금속표면의 오염물질이나 녹을 제거하는 녹제거제 제조방법에 관한 것으로 녹제거후 금속표면에 친수성 방청막을 형성시켜 일정기간 방청성을 유지하는 동시에 생분해도가 높은 약품류의 사용으로 사용후 별도의 폐수처리 절차없이 폐기가 가능하며 무기산류로 제조된 녹제거제의 사용상의 불편함이나 냄새발생에 의한 인체에 대한 유해성을 없앤 친환경 녹제거제 제조 방법이다.The present invention relates to a method for manufacturing a rust remover that removes contaminants or rust from a metal surface by using a biodegradable material. It can be disposed of without a separate wastewater treatment process after use, and it is an eco-friendly rust remover manufacturing method that eliminates the inconvenience of using rust removers made of inorganic acids or the harmfulness to the human body due to odor generation.
금속 관련 산업이 발달함에 따라 철및 비철금속류를 사용한 다양한 금속제품의 생산이 증가하고 있으나 생산이 이루어지는 만큼 이들 제품의 운송 보관시 발생하는 부식으로 인한 산업적 손실이 증대되고 있다.As the metal-related industry develops, the production of various metal products using ferrous and non-ferrous metals is increasing, but industrial losses due to corrosion occurring during transportation and storage of these products are increasing as much as production is being made.
미국의 경우 GNP의 3% 정도가 부식에 의한 산업적 손실이며 차동차 산업의 경우 부식에 의한 차량 결함도 심각한 상황이다.In the case of the United States, about 3% of GNP is industrial loss due to corrosion, and vehicle defects due to corrosion are also a serious situation in the automobile industry.
이러한 부식에 의해 생성된 금속 제품류의 녹을 제거하기 위해 대부분 환원제로 무기산으로 녹제거제를 제조하거나 유기산, 유기염에 킬레이트제,침전제,냄새제거제등을 사용하여 녹제거제를 제조하나 여기에 사용되는 침전제나 냄새 제거제등은 대부분 유해화합물질이 대부분이다.In order to remove the rust of metal products generated by such corrosion, rust removers are mostly manufactured with inorganic acids as reducing agents, or by using chelating agents, precipitants, odor eliminators, etc. with organic acids and organic salts. Odor removers are mostly composed of harmful chemicals.
특히 황화수소의 경우 독성이 강해 OSHA,TSCA등에 유해물질로 등록되어 있어 그 사용을 제한하고 있으며 특히 방청제로 사용되는 약품들은 아질산염이나 2가 아민류등을 사용하는데 이들 약품은 유럽연합의 TRGS 615에 사용상에 규제된 유해약품들이다. 또한 벤조 트리아졸등을 사용하고 있으나 벤조 트리아졸류의 경우 생분해가 일어나지 않는 물질로 유럽연합의 REACH(Registration,Evaluation,Authorisation & Restriction of Chemicals)규제 예비물질로 등록되어있어 친 환경적이지 못하다. 또한 종래의 대부분의 녹제거제는 방청기능이 없어 녹제거후 별도의 방청처리를 하여야만 했고 녹제어 기능이 있는 제품들의 경우 금속표면에 피막형성을 시키므로 자동차 부품류나 기계부품류등 대부분 녹제거후 표면 상태의 변화를 요하지 않는 제품에는 사용하지 못하는 단점이 있다. 이러한 녹제거제의 선행기술로는 대한민국 등록특허 제 102280544호 "은 나노 입자를 이용한 페인트 박리제, 녹제거제,탈지제 제조방법" (등록일자 : 2021.7.16)과, 대한민국 등록특허 제102155545호 "친환경 녹제어제 및 그 사용방법(등록일자: 2020.9.8) 대한민국 등록특허 제101801002호"녹제거 조성물 및 이를 이용한 녹제거 방법"(등록일자: 2017.11.17)등이 개시 되어 있다.In particular, hydrogen sulfide is highly toxic and is registered as a hazardous substance in OSHA, TSCA, etc., so its use is limited. They are regulated hazardous drugs. In addition, benzotriazoles are used, but benzotriazoles are non-biodegradable substances and are not environmentally friendly as they are registered as REACH (Registration, Evaluation, Authorization & Restriction of Chemicals) regulatory preliminary substances in the European Union. In addition, most conventional rust removers do not have a rust prevention function, so they had to be treated separately after rust removal. In the case of products with a rust control function, a film is formed on the metal surface, so most of the surface state after rust removal, such as automobile parts and machine parts Products that do not require change have the disadvantage of not being usable. Prior art of such a rust remover includes Republic of Korea Patent No. 102280544 "Method of manufacturing paint stripper, rust remover, and degreaser using silver nanoparticles" (Registration date: July 16, 2021) and Republic of Korea Patent No. 102155545 "Eco-friendly rust control agent" And how to use it (registration date: 2020.9.8) Korean Patent Registration No. 101801002 "Rust removal composition and rust removal method using the same" (registration date: 2017.11.17), etc. are disclosed.
본 발명의 목적은 무기산등의 사용에 따른 녹제거제 사용시 발생되는 환경오염 및 사용상의 단점을 보완하고, 녹제거후 금속표면에 녹전이 물질을 생성치 않아 금속의 표면 상태를 색변화 없이 유지 시켜 사용 대상물의 범위를 넓히고 녹제거후 발생되는 2차 부식발생을 제거하여 별도의 방청처리없이 금속제품류를 사용할 수 있는 방청기능을 첨가하여 생산과정의 단순화에 따른 경제적효과를 증대하며 생분해도가 높은 약품류를 사용하여 사용후 폐기시 별도의 폐기 절차없이 페기할수 있는 환경 친화적인 녹제거제를 만드는데 발명의 목적이 있다.The purpose of the present invention is to supplement the environmental pollution and disadvantages in use that occur when using a rust remover due to the use of inorganic acid, etc., and to maintain the surface state of the metal without color change by not generating a rust transition material on the metal surface after rust removal. Chemicals with high biodegradability and increased economic effects due to simplification of the production process by adding anti-corrosion function that allows metal products to be used without separate anti-rust treatment by widening the range of objects and removing secondary corrosion that occurs after rust removal An object of the invention is to make an environmentally friendly rust remover that can be disposed of without a separate disposal procedure when discarded after use.
상기 목적을 달성하기 위해서 금속표면의 오염물질 및 녹제거 성분을 혼합하는 제 1 혼합 교반 단계, 방청성분을 혼합하는 제 2 혼합 교반 단계, 금속표면에 친수성 방청피막을 형성시키는 약품을 혼합 교반시키는 제 3 혼합 교반 단계로 구성된 것을 특징으로 한다.In order to achieve the above object, the first mixing and stirring step of mixing the contaminants and rust removal components on the metal surface, the second mixing and stirring step of mixing the rust preventive component, and the mixing and stirring agent for forming a hydrophilic rust preventive film on the metal surface It is characterized in that it consists of 3 mixing and stirring steps.
또한 상기 혼합약품은 증류수 1000중량부에 글리콘산 100내지 200중량부, 구연산 50내지 100중량부, 사과산 25내지 50중량부, 글루콘산 나트륨 30내지 50중량부, 카프릴산 나트륨 30내지 50중량부, 폴리비닐알코올 20내지 50중량부, 폴리솔베이트(80), 20내지 50중량부인 것을 특징으로 한다.In addition, the mixed medicine is 100 to 200 parts by weight of distilled water, 100 to 200 parts by weight of glycolic acid, 50 to 100 parts by weight of citric acid, 25 to 50 parts by weight of malic acid, 30 to 50 parts by weight of sodium gluconate, 30 to 50 parts by weight of sodium caprylate Part, polyvinyl alcohol 20 to 50 parts by weight, polysorbate 80, characterized in that 20 to 50 parts by weight.
본 발명의 방청기능이 있는 녹제거제는 생분해도가 높은 식품 발효물, 식품첨가물등을 사용하여 인체에 무해하며, 또한 별도의 폐기 과정없이 사용후 폐기할수 있는 생분해도가 높으며, 유기산을 주 환원제로 사용하여 사용상의 위험성이나 냄새등의 불편함이 없으며 금속표면의 녹 제거후 수용성 방청 피막을 형성시켜 녹제거후 별도의 방청공정 없이 사용할 수 있는 효과를 가지고 있으며, 녹제어제나 일반 인산이나 인산염으로 구성된 제품과 달리 사용후 금속표면의 변색이나 상태 변화를 야기 시키지 않아 정밀 기계부품, 자동차 부품류등의 녹제거에 공히 사용 될수 있는 장점을 가지고 있다.The rust remover with anti-rust function of the present invention is harmless to the human body by using fermented food and food additives with high biodegradability, and also has high biodegradability that can be discarded after use without a separate disposal process, and organic acid is used as the main reducing agent. There is no danger of use or inconvenience such as smell, and it has the effect of forming a water-soluble rust-preventive film after removing rust from the metal surface so that it can be used without a separate rust-prevention process after removing rust. Unlike other products, it does not cause discoloration or state change on the metal surface after use, so it has the advantage that it can be used for rust removal of precision machine parts and automobile parts.
도 1 은 방청기능이 있는 친환경 녹제거제 제조방법의 공정순서도이다.1 is a process flow chart of a method for manufacturing an eco-friendly rust remover having a rust-preventing function.
이하, 첨부된 도면을 참조하여 본 발명의 제조방법을 상세히 설명하고자 한다.Hereinafter, the manufacturing method of the present invention will be described in detail with reference to the accompanying drawings.
도 1에 도시된 바와 같이 본 발명의 증류수 1000중량부에 글리콘 산 100 내지 200 중량부, 구연산 50내지 100중량부, 사과산 25내지 50중량부를 혼합 교반기에 넣어 혼합 용해 시키는 제 1 혼합 교반단계(S10), 상기 혼합 용해된 용액에 글루콘산 나트륨 30내지 50중량부, 카프릴산 나트륨 30내지 50중량부를 넣고 혼합 용해 시키는 제 2 혼합 교반 단계(S20) 상기 혼합 용해된 용액에 폴리비닐알콜 20내지 50중량부, 폴리솔베이트(80) 20내지 50중량부를 넣고 혼합 용해시키는 제 3 혼합 교반 단계(S30)로 구성 된다.As shown in FIG. 1, 100 to 200 parts by weight of glycolic acid, 50 to 100 parts by weight of citric acid, and 25 to 50 parts by weight of malic acid are added to 1000 parts by weight of distilled water of the present invention in a mixing stirrer to mix and dissolve the first mixing and stirring step ( S10), a second mixing and stirring step (S20) of adding 30 to 50 parts by weight of sodium gluconate and 30 to 50 parts by weight of sodium caprylate to the mixed and dissolved solution and mixing and dissolving 20 to 50 parts by weight of polyvinyl alcohol in the mixed and dissolved solution It consists of a third mixing and stirring step (S30) of mixing and dissolving 50 parts by weight and 20 to 50 parts by weight of polysorbate (80).
상기 혼합약품은 증류수 1000중량부에 글리콘산 100내지 200중량부, 구연산 50내지 100중량부, 사과산 25내지 50중량부, 글루콘산 나트륨 30내지 50중량부, 카프릴산 나트륨 30내지 50중량부, 폴리비닐알코올 20내지 50중량부, 폴리솔베이트(80), 20내지 50중량부로 구성 되어 있다The mixed medicine is 100 to 200 parts by weight of distilled water, 100 to 200 parts by weight of glycolic acid, 50 to 100 parts by weight of citric acid, 25 to 50 parts by weight of malic acid, 30 to 50 parts by weight of sodium gluconate, 30 to 50 parts by weight of sodium caprylate , Polyvinyl alcohol 20 to 50 parts by weight, polysorbate 80, composed of 20 to 50 parts by weight
상기의 구성에 따른 방청기능이 있는 녹제거제 제조방법의 과정은 다음과 같다.The process of manufacturing a rust remover having an anti-rust function according to the above configuration is as follows.
도 1)에 도시된 바와 같이As shown in Figure 1)
제 1 혼합 교반 단계(S10)는 녹 및 오염물 제거기능이 있는 글리콘산,구연산,사과산을 증류수와 함계 교반기를 이용하여 실온 섭씨(23도)에서 25 RPM/min.의 속도로 20분간 교반시킨다. 글루콘산은 생분해율이 99%이상이 친환경물질로 금속류의 표면세척과 녹제거 기능이 있고 구연산은 생분해도가 높은 식품 첨가물로 녹제거 및 산세척 작용이 있다.In the first mixing and stirring step (S10), glycolic acid, citric acid, and malic acid, which have a function of removing rust and contaminants, are stirred for 20 minutes at a speed of 25 RPM/min. at room temperature (23 degrees Celsius) using a stirrer with distilled water. . Gluconic acid is an eco-friendly material with a biodegradability of more than 99% and has functions of cleaning the surface of metals and removing rust. Citric acid is a food additive with high biodegradability and has rust removal and pickling functions.
사과산은 사용된 유기산의 환원기능을 촉진시키는 기능이 있어 구연산과 2:1의 비율로 혼합 사용시 가장 효과가 좋다Malic acid has the function of promoting the reducing function of the organic acid used, so it is most effective when mixed with citric acid at a ratio of 2:1.
제 2 혼합 교반 단계는 상기 제 1 혼합 용해 단계 혼합액에 글루콘산 나트륨 50중량부, 카프릴산 나트륨 50 중량부를 넣고 25RPM/min의 속도로 다시 20분간 교반시켜 완전 용해 시킨다In the second mixing and stirring step, 50 parts by weight of sodium gluconate and 50 parts by weight of sodium caprylate are added to the mixed solution of the first mixing and dissolving step, and stirred at a speed of 25 RPM/min for 20 minutes to completely dissolve them.
글루콘산 나트륨은 생분해성이 높은 식품첨가물로 킬레이트작용이 있어 유리된 금속이온과 킬레이트를 형성시키며 철 및 비철금속류에 좋은 방청성을 가지고 있다. 제조시 사용량 미만을 사용하면 방청력이 약하고 이상을 사용시 녹제거능력을 저하시킨다.Sodium gluconate is a food additive with high biodegradability. It has a chelating action, forms a chelate with free metal ions, and has good anti-corrosion properties for ferrous and non-ferrous metals. If less than the amount used in manufacturing is used, rust prevention is weak, and if more is used, rust removal ability is lowered.
카프릴산 나트륨은 철금속류에 좋은 방청성을 지니며 특히 금속표면의 수용성 피막형성시 안정제 역할을 한다. 적정량이상 사용시 비 경제적이다.Sodium caprylate has good anti-corrosive properties for ferrous metals and acts as a stabilizer when forming a water-soluble film on the metal surface. It is uneconomical when used in an appropriate amount.
제 3 혼합 교반 단계(S30)는 제 2 혼합 교반 단계에서 생성된 혼합액에 폴리비닐알콜 20내지 50중량부 폴리솔베이트(80) 20내지 50중량부를 넣고 교반기의 온도를 섭씨 40도(+/-3)도로 하여 50RPM/min으로 40분간 교반시켜 혼합액을 만든다.In the third mixing and stirring step (S30), 20 to 50 parts by weight of polyvinyl alcohol and 20 to 50 parts by weight of polysorbate (80) are added to the mixed solution produced in the second mixing and stirring step, and the temperature of the stirrer is set to 40 degrees Celsius (+/- 3) Also, stir at 50 RPM/min for 40 minutes to make a mixed solution.
폴리비닐알콜은 수용성폴리머로 생분해성이 좋고 금속표면에 피막을 형성시키는 기반물질로 적정량이상 사용시 사용후 피막형성시 건조상의 문제를 야기 시킨다.Polyvinyl alcohol is a water-soluble polymer that has good biodegradability and is a base material that forms a film on a metal surface. When used in an appropriate amount, polyvinyl alcohol causes drying problems when forming a film after use.
폴리 솔베이트(80)은 폴리비닐과 함께 수용성 방청피막을 형성시키며 비철금속류의 방청에 좋은 효과를 가지고 있다. 적정량을 사용 하여야 폴리비닐 알코올과 수용성방청피막을 안정적으로 생성시킬수있다.Polysorbate 80 forms a water-soluble rust-preventive film together with polyvinyl and has a good effect on preventing non-ferrous metals from rusting. It is possible to stably create polyvinyl alcohol and a water-soluble rust-preventive film only when an appropriate amount is used.
폴리비닐알코올과 1:1의 비율로 사용시 최적의 방청피막을 형성 시킨다.When used in a ratio of 1:1 with polyvinyl alcohol, it forms an optimal anti-rust film.
본 발명에 의해 제조되는 기화성 방청제의 조성비에 따른 녹제거 능력과,방청실험,생분해도를 측정하기 위해 다음과 같이 각각의 샘플을 제조하였다.Each sample was prepared as follows to measure the rust removal ability, rust prevention test, and biodegradability according to the composition ratio of the vaporizable rust inhibitor prepared according to the present invention.
샘플 1sample 1
증류수 1000중량부에 글리콜산 200중량부, 구연산 50중량부, 사과산 25중량부를 넣고 교반기를 이용하여 실온에서 25RPM/min으로 20분간 혼합하여 제 1 혼합액을 만든후 여기에 글루콘산 나트륨 30중량부, 카프릴산 나트륨 30중량부를 넣고 다시 25RPM/min으로 20분간 혼합시켜 제2 혼합액을 만든다. 상기액에 폴리비닐알콜 20중량부 폴리 솔베이트(80) 20중량부를 넣고 50RPM/min으로 40분간 교반시켜 샘플 용액을 제조한다.200 parts by weight of glycolic acid, 50 parts by weight of citric acid, and 25 parts by weight of malic acid were added to 1000 parts by weight of distilled water and mixed for 20 minutes at 25 RPM/min at room temperature using an agitator to make a first mixed solution, followed by 30 parts by weight of sodium gluconate, Add 30 parts by weight of sodium caprylate and mix again at 25 RPM/min for 20 minutes to make a second mixed solution. A sample solution was prepared by adding 20 parts by weight of polyvinyl alcohol and 20 parts by weight of polysorbate (80) to the solution and stirring at 50 RPM/min for 40 minutes.
샘플 2sample 2
증류수 1000중량부에 글리콜산 200중량부, 구연산 100중량부, 사과산 50중량부를 넣고 교반기를 이용하여 실온에서 25RPM/min으로 20분간 혼합하여 제 1 혼합액을 만든후 여기에 글루콘산 나트륨 50중량부, 카프릴산 나트륨 50중량부를 넣고 다시 25RPM/min으로 20분간 혼합시켜 제2 혼합액을 만든다. 상기액에 폴리비닐알콜 50중량부 폴리 솔베이트(80) 50중량부를 넣고 50RPM/min으로 40분간 교반시켜 샘플 용액을 제조한다.200 parts by weight of glycolic acid, 100 parts by weight of citric acid, and 50 parts by weight of malic acid were added to 1000 parts by weight of distilled water and mixed at room temperature at 25 RPM/min for 20 minutes using an agitator to make a first mixed solution, and then 50 parts by weight of sodium gluconate, Add 50 parts by weight of sodium caprylate and mix again at 25 RPM/min for 20 minutes to make a second mixed solution. A sample solution was prepared by adding 50 parts by weight of polyvinyl alcohol and 50 parts by weight of polysorbate (80) to the solution and stirring at 50 RPM/min for 40 minutes.
샘플 3sample 3
증류수 1000중량부에 글리콜산 200중량부, 구연산100중량부, 사과산 50중량부를 넣고 교반기를 이용하여 실온에서 25RPM/min으로 20분간 혼합하여 제 1 혼합액을 만든후 여기에 글루콘산 나트륨 50중량부, 카프릴산 나트륨 50중량부를 넣고 다시 25RPM/min으로 20분간 혼합시켜 제2 혼합액을만든다. 상기액에 폴리비닐알콜 20중량부 폴리 솔베이트(80) 20중량부를 넣고 50RPM/min으로 40분간 교반시켜 샘플 용액을 제조한다Add 200 parts by weight of glycolic acid, 100 parts by weight of citric acid, and 50 parts by weight of malic acid to 1000 parts by weight of distilled water and mix for 20 minutes at 25 RPM/min at room temperature using an agitator to make a first mixed solution, 50 parts by weight of sodium gluconate, Add 50 parts by weight of sodium caprylate and mix again at 25 RPM/min for 20 minutes to prepare a second mixed solution. 20 parts by weight of polyvinyl alcohol and 20 parts by weight of polysorbate (80) were added to the solution and stirred at 50 RPM/min for 40 minutes to prepare a sample solution.
샘플 4sample 4
증류수 1000중량부에 글리콜산 200중량부, 구연산 100중량부, 사과산 50중량부를 넣고 교반기를 이용하여 실온에서 25RPM/min으로 20분간 혼합하여 제 1 혼합액을 만든후 여기에 글루콘산 나트륨 40중량부, 카프릴산 나트륨 40중량부를 넣고 다시 25RPM/min으로 20분간 혼합시켜 제2 혼합액을 만든다. 상기액에 폴리비닐알콜 30중량부 폴리 솔베이트(80) 30중량부를 넣고 50RPM/min으로 40분간 교반시켜 샘플 용액을 제조한다200 parts by weight of glycolic acid, 100 parts by weight of citric acid, and 50 parts by weight of malic acid were added to 1000 parts by weight of distilled water and mixed at room temperature at 25 RPM/min for 20 minutes using a stirrer to make a first mixed solution, followed by 40 parts by weight of sodium gluconate, Add 40 parts by weight of sodium caprylate and mix again at 25 RPM/min for 20 minutes to make a second mixed solution. 30 parts by weight of polyvinyl alcohol and 30 parts by weight of polysorbate (80) were added to the solution and stirred at 50 RPM/min for 40 minutes to prepare a sample solution.
샘플 5sample 5
증류수 1000중량부에 글리콜산 150중량부, 구연산 60중량부, 사과산 30중량부를 넣고 교반기를 이용하여 실온에서 25RPM/min으로 20분간 혼합하여 제 1 혼합액을 만든후 여기에 글루콘산 나트륨 30중량부, 카프릴산 나트륨 30중량부를 넣고 다시 25RPM/min으로 20분간 혼합시켜 제2 혼합액을 만든다. 상기액에 폴리비닐알콜 40중량부 폴리 솔베이트(80) 40중량부를 넣고 50RPM/min으로 40분간 교반시켜 샘플 용액을 제조한다Add 150 parts by weight of glycolic acid, 60 parts by weight of citric acid, and 30 parts by weight of malic acid to 1000 parts by weight of distilled water and mix for 20 minutes at 25 RPM/min at room temperature using an agitator to make a first mixed solution, then 30 parts by weight of sodium gluconate, Add 30 parts by weight of sodium caprylate and mix again at 25 RPM/min for 20 minutes to make a second mixed solution. 40 parts by weight of polyvinyl alcohol and 40 parts by weight of polysorbate (80) were added to the solution and stirred at 50 RPM/min for 40 minutes to prepare a sample solution.
녹제거후 금속표면 관찰실험Metal surface observation test after rust removal
위의 5 가지 혼합물 샘플을 이용하여 금속시편의 녹을 제거후 금속표면을 현미경 관찰 하였다..After removing the rust of the metal specimen using the above 5 mixture samples, the metal surface was observed under a microscope.
Test 금속시편: QQ-S-698탄소강(5X7.5cm)Test metal specimen: QQ-S-698 carbon steel (5X7.5cm)
녹발생절차: 상기시편을 소금물 5%용액에 담근후 항온조 온도 섭씨 40도에서 24시간 장치하여 녹을 발생 시킨다.Rust generation procedure: After immersing the specimen in a 5% salt water solution, it is placed in a constant temperature bath at 40 degrees Celsius for 24 hours to generate rust.
실험절차 1) 녹발생 절차에 의해 ,녹을 형성시킨 실험시편을 각기의 샘플용액에 20분 함침하여 녹제거후 상온에서 30분 건조후 금속표면을 현미경 관찰 하여 금속표면을 관찰 하였다.Experimental procedure 1) By the rust generation procedure, the test specimens in which rust was formed were immersed in each sample solution for 20 minutes to remove rust, and then dried at room temperature for 30 minutes, and then the metal surface was observed under a microscope.
표 1)Table 1)
실험결과 샘플1~5 모두 금속표면의 녹이 깨끗이 제거되고 금속표면에 변색등이 없는 것을 확인하였다.As a result of the experiment, it was confirmed that the rust on the metal surface was cleanly removed and there was no discoloration on the metal surface in all samples 1 to 5.
접촉성 방청실험(CONTACT TEST)CONTACT TEST
실험시편: QQ-S-698,T3 구리, LY12 알루미늄,Test specimen: QQ-S-698, T3 copper, LY12 aluminum,
실험시편 녹발생절차: 상기시편을 소금물 5%용액에 담근후 항온조 온도 섭씨 40도에서 24시간 장치하여 녹을발생 시킨다.Test specimen rust generation procedure: After immersing the specimen in a 5% salt water solution, rust is generated by placing the specimen in a constant temperature bath at 40 degrees Celsius for 24 hours.
실험절차 1) 녹발생 절차에 의해 ,녹을 형성시킨 실험시편을 각기의 샘플용액에 20분 함침하여 녹제거후 상온에서 30분 건조시킨다.Experimental procedure 1) By the rust generation procedure, the test specimens in which rust was formed were immersed in each sample solution for 20 minutes to remove rust, and then dried at room temperature for 30 minutes.
2) 500ml Test Jar에 Lucite를 넣고 그위에 준비된 금속 시편을 장착하고 글리세린 25% 용액을 30ml넣고 Test Jar를 CAP을 이용하여 밀봉한다.2) Put Lucite in a 500ml Test Jar, mount the prepared metal specimen on it, put 30ml of a 25% glycerin solution, and seal the Test Jar using a CAP.
3) 항온조 온도 섭씨 50도에 4)의 준비된 Jar를 넣고 72시간후 부식상태를 관찰한다.3) Put the jar prepared in 4) in a thermostat at a temperature of 50 degrees Celsius and observe the corrosion state after 72 hours.
- 평가 : 부식 방지 효과는 아래 요구 사항을 기반으로 한다.- Evaluation: The anti-corrosion effect is based on the requirements below.
0 ~ 2 등급은 이 시험에 합격한 것으로 간주한다.Grades 0 to 2 are considered to have passed this test.
3 ~ 6 등급은 시험 실패로 간주한다.Grades 3 to 6 are considered test failures.
도표 2)diagram 2)
실험결과 탄소강및 구리, 알루미늄의 비철금속류에도 좋은 방청효과가 있음을 알수 있다.As a result of the experiment, it can be seen that carbon steel and non-ferrous metals such as copper and aluminum have good anti-rust effects.
생분해성 실험biodegradability experiment
샘플로 제조된 녹제거제의 생화학분해성을 KS/ISO/7827:1994(2018 CONFIRMED) 방법에 의해 측정하였다.The biochemical degradability of the rust remover prepared as a sample was measured by the KS/ISO/7827:1994 (2018 CONFIRMED) method.
실험방법: KS/ISO/7827:1994(2018 CONFIRMED)Test method: KS/ISO/7827:1994 (2018 CONFIRMED)
배양온도: 섭씨(23+/-2)도Incubation temperature: (23+/-2) degrees Celsius
분석장비: TOC ANALYSER(총 유기탄소분석기)Analysis equipment: TOC ANALYSER (total organic carbon analyzer)
분석기간: 21 일Analysis period: 21 days
[표 3][Table 3]
상기 실험결과 샘플 1,2,3,4,5모두 93% 이상의 높은 생분해율을 확인 하였다.As a result of the above experiment, samples 1, 2, 3, 4, and 5 all confirmed a high biodegradation rate of 93% or more.
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KR101801002B1 (en) | 2017-06-01 | 2017-11-23 | 이원호 | Derusting Agent Composition and Derusting Method using it |
KR102155545B1 (en) | 2018-08-10 | 2020-09-14 | 현대정밀화학 주식회사 | Eco-friendly rust control composition and method for using the same |
KR102280544B1 (en) | 2019-03-05 | 2021-07-23 | 주식회사 조은기업 | Manufacturing method of Paint remover,Rust cleaner,Degreaser by use of Silver nanoparticles |
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