KR20230091379A - Method of manufacturing an eco-friendly anti-corrison release coating agent - Google Patents
Method of manufacturing an eco-friendly anti-corrison release coating agent Download PDFInfo
- Publication number
- KR20230091379A KR20230091379A KR1020210180442A KR20210180442A KR20230091379A KR 20230091379 A KR20230091379 A KR 20230091379A KR 1020210180442 A KR1020210180442 A KR 1020210180442A KR 20210180442 A KR20210180442 A KR 20210180442A KR 20230091379 A KR20230091379 A KR 20230091379A
- Authority
- KR
- South Korea
- Prior art keywords
- release agent
- binder
- synthetic oil
- manufacturing
- eco
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- 239000011248 coating agent Substances 0.000 title 1
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 39
- 239000003921 oil Substances 0.000 claims abstract description 23
- 235000019198 oils Nutrition 0.000 claims abstract description 23
- 238000005260 corrosion Methods 0.000 claims abstract description 22
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims abstract description 22
- 235000013311 vegetables Nutrition 0.000 claims abstract description 21
- 239000011230 binding agent Substances 0.000 claims abstract description 20
- 229920000642 polymer Polymers 0.000 claims abstract description 17
- 238000003756 stirring Methods 0.000 claims abstract description 16
- 238000000034 method Methods 0.000 claims abstract description 15
- 238000002156 mixing Methods 0.000 claims abstract description 13
- 239000000654 additive Substances 0.000 claims abstract description 12
- 230000000996 additive effect Effects 0.000 claims abstract description 12
- 239000012153 distilled water Substances 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000003054 catalyst Substances 0.000 claims abstract description 10
- 239000000725 suspension Substances 0.000 claims abstract description 10
- 239000003112 inhibitor Substances 0.000 claims abstract description 9
- 239000003822 epoxy resin Substances 0.000 claims abstract description 8
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 8
- 239000004094 surface-active agent Substances 0.000 claims abstract description 7
- 239000004593 Epoxy Substances 0.000 claims abstract description 6
- 235000021388 linseed oil Nutrition 0.000 claims abstract description 6
- 239000000944 linseed oil Substances 0.000 claims abstract description 6
- 150000002148 esters Chemical class 0.000 claims abstract description 5
- 230000001590 oxidative effect Effects 0.000 claims abstract description 5
- 238000001816 cooling Methods 0.000 claims abstract description 3
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 14
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 claims description 10
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 8
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims description 6
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical group [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 5
- 235000019333 sodium laurylsulphate Nutrition 0.000 claims description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 4
- 239000011787 zinc oxide Substances 0.000 claims description 4
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims description 3
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 230000032050 esterification Effects 0.000 claims 1
- 238000005886 esterification reaction Methods 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 239000012855 volatile organic compound Substances 0.000 abstract description 12
- 238000010276 construction Methods 0.000 abstract description 8
- 230000007797 corrosion Effects 0.000 abstract description 5
- 206010000372 Accident at work Diseases 0.000 abstract description 3
- 230000007547 defect Effects 0.000 abstract description 3
- 230000002194 synthesizing effect Effects 0.000 abstract description 2
- 238000009415 formwork Methods 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- SZKKRCSOSQAJDE-UHFFFAOYSA-N Schradan Chemical group CN(C)P(=O)(N(C)C)OP(=O)(N(C)C)N(C)C SZKKRCSOSQAJDE-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- BBFLWGXNVUURKR-UHFFFAOYSA-N C(C)C(CC(C(=O)O)=C)CCCC.C(C)C(CC(C(=O)O)=C)CCCC Chemical compound C(C)C(CC(C(=O)O)=C)CCCC.C(C)C(CC(C(=O)O)=C)CCCC BBFLWGXNVUURKR-UHFFFAOYSA-N 0.000 description 1
- HIBWGGKDGCBPTA-UHFFFAOYSA-N C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 HIBWGGKDGCBPTA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000013556 antirust agent Substances 0.000 description 1
- 238000009435 building construction Methods 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B28—WORKING CEMENT, CLAY, OR STONE
- B28B—SHAPING CLAY OR OTHER CERAMIC COMPOSITIONS; SHAPING SLAG; SHAPING MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
- B28B7/00—Moulds; Cores; Mandrels
- B28B7/38—Treating surfaces of moulds, cores, or mandrels to prevent sticking
- B28B7/388—Treating surfaces of moulds, cores, or mandrels to prevent sticking with liquid material, e.g. lubricating
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M177/00—Special methods of preparation of lubricating compositions; Chemical modification by after-treatment of components or of the whole of a lubricating composition, not covered by other classes
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/36—Release agents or mold release agents
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Ceramic Engineering (AREA)
- Mechanical Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
Abstract
본 발명은 친환경 부식방지용 이형제 제조방법에 관한 것으로서, 아마인유에 증류수와 계면활성제를 넣고 80℃에서 20분 동안 교반하여 현탁액을 수득하고, 수득한 80℃의 현탁액에 에폭시 수지를 넣고 20분 동안 교반하여 산화가교결합(Oxidative cross-link)을 통해 에폭시 에스테르화(Epoxy ester) 합성하여 식물성 합성오일을 수득하는 단계 및 방청제에 증류수로 희석된 촉매를 드랍하면서 3시간 동안 교반한 교반액에 고분자 첨가제를 첨가하여 80℃에서 1시간 교반 후 냉각하여 바인더를 수득하는 단계 및 수득한 상기 식물성 합성오일과 상기 바인더를 3 : 7의 비율로 배합하여 이형제를 수득하는 단계를 포함하여 이루어진다.
상기와 같은 본 발명에 의하면, 기존 휘발성 유기화합물(VOCs)을 대체하여 식물성 합성오일을 사용함에 따라 친환경적이면서 인체에 무해하여 작업장 환경을 개선할 수 있을 뿐 아니라 산업재해사고를 방지할 수 있다.
또한, 고분자를 첨가하여 방청성능이 향상된 바인더와 식물성 합성오일의 배합비를 최적화하여 이형성 및 내식성이 크게 향상됨에 따라 양생되는 콘크리트의 불량률이 크게 감소하여 공사비용을 현저하게 절감할 수 있다.The present invention relates to a method for manufacturing an eco-friendly anti-corrosive release agent, wherein distilled water and a surfactant are added to linseed oil and stirred at 80° C. for 20 minutes to obtain a suspension, and an epoxy resin is added to the obtained suspension at 80° C. and stirred for 20 minutes. To obtain a vegetable synthetic oil by synthesizing epoxy ester through oxidative cross-link and adding a polymer additive to a stirring solution stirred for 3 hours while dropping a catalyst diluted with distilled water on a rust inhibitor It comprises the steps of adding, stirring at 80 ° C. for 1 hour and then cooling to obtain a binder, and mixing the obtained vegetable synthetic oil and the binder in a ratio of 3: 7 to obtain a release agent.
According to the present invention as described above, as vegetable synthetic oil is used to replace existing volatile organic compounds (VOCs), it is environmentally friendly and harmless to the human body, thereby improving the workplace environment and preventing industrial accidents.
In addition, by optimizing the blending ratio of a binder with improved anti-rust performance by adding a polymer and vegetable synthetic oil, the release property and corrosion resistance are greatly improved, so the defect rate of cured concrete is greatly reduced, and construction costs can be significantly reduced.
Description
본 발명은 친환경 부식방지용 이형제 제조방법에 관한 것으로서, 보다 상세하게는 기존 휘발성 유기화합물(VOCs)을 대체하여 식물성 합성오일을 사용함에 따라 친환경적이면서 인체에 무해하고, 고분자를 첨가하여 방청성능이 향상된 바인더와 식물성 합성오일의 배합비를 최적화하여 이형성 및 내식성이 크게 향상된 친환경 부식방지용 이형제 제조방법에 관한 것이다.The present invention relates to a method for manufacturing an eco-friendly anti-corrosion release agent, and more particularly, to a binder that is environmentally friendly, harmless to the human body, and has improved anti-rust performance by adding a polymer by using vegetable synthetic oil in place of existing volatile organic compounds (VOCs). It relates to a method for manufacturing an eco-friendly anti-corrosion release agent with significantly improved release properties and corrosion resistance by optimizing the mixing ratio of and vegetable synthetic oil.
일반적으로 건축물 공사에서 거푸집은 전체 공사비면에서 약 10%, 그리고, 전체 공사기간면에서 25%를 차지할 정도로 비중이 크고, 그 밖에 품질, 안전 측면에서도 매우 중요한 공사 중 한 부분을 차지하고 있다.In general, in building construction, formwork accounts for about 10% of the total construction cost and 25% of the total construction period, and it is one of the very important constructions in terms of quality and safety.
건축물을 공사하는 경우, 제작하고자 하는 콘크리트 구조물의 형상에 맞도록 알루미늄과 같은 금속 거푸집을 만든 다음, 이 거푸집 속에 콘크리트를 주입한 후 콘크리트가 양생된 후에는 거푸집을 분리(탈형)하게 된다.In the case of constructing a building, a metal formwork such as aluminum is made to fit the shape of the concrete structure to be manufactured, concrete is injected into the formwork, and after the concrete is cured, the formwork is separated (demolded).
이와 같이, 거푸집을 분리하는 과정에서 콘크리트와 거푸집 간의 결합력에 의해 거푸집이 쉽게 분리되지 않거나 또는 콘크리트의 일부가 떨어져나가 매끄러운 표면마감이 어려우며, 그 떨어져 나간 부분을 수작업으로 일일이 메워야 하므로 공사기간과 공사비용을 상승시키는 요인이 된다.In this way, in the process of separating the formwork, the formwork is not easily separated due to the bonding force between the concrete and the formwork, or a part of the concrete falls off, making it difficult to finish the smooth surface, and the separated parts must be manually filled, which reduces the construction period and construction cost. becomes a factor that increases
이와 같은 문제점을 해결하기 위해, 거푸집의 내부 표면에 이형제(박리제)를 도포하는데, 이 때 박리제로서 폐유, 윤활유, 등유, 경유 등을 단독으로 사용하거나 이에 적당량의 점착제를 용해시킨 것을 사용하고 있다.In order to solve this problem, a release agent (release agent) is applied to the inner surface of the formwork. At this time, waste oil, lubricating oil, kerosene, light oil, etc. are used alone or an appropriate amount of adhesive is dissolved as the release agent.
그러나, 상기와 같은 석유 성분을 함유하는 이형제는 화재위험성이 있을 뿐 아니라, 석유 성분에 포함된 휘발성 유기화합물(Volatile Organic Compounds, VOCs)이 인체에 암을 유발하는 요인으로 작용한다.However, the release agent containing petroleum components as described above has a fire hazard, and volatile organic compounds (VOCs) contained in petroleum components act as a factor inducing cancer in the human body.
또한, 위와 같은 휘발성 유기화합물은 산화과정을 통해 오존과 같은 이차 생성 물질들을 만들어내기 때문에 질소산화물과 함께 광화학 스모그를 일으키는 주요원인으로 작용할 뿐 아니라, 기체상 반응을 최종적으로 거친 휘발성 유기화합물은 CO2와 같은 온실가스를 배출하는 문제점이 있다.In addition, since the above volatile organic compounds produce secondary substances such as ozone through an oxidation process, they act as a major cause of photochemical smog along with nitrogen oxides . There is a problem of emitting greenhouse gases such as
따라서, 최근 기후변화를 막기 위해 탄소중립 정책을 추진하는 국제사회의 노력에 부응하면서, 작업자의 건강을 해치지 않으면서 안전하게 사용할 수 있는 친환경 이형제의 개발이 절실하게 요구되고 있는 실정이다.Therefore, the development of an eco-friendly release agent that can be safely used without harming the health of workers is urgently required while responding to the efforts of the international community to promote carbon neutral policy to prevent recent climate change.
본 발명은 상기와 같은 문제점을 해결하기 위해 안출된 것으로서, 본 발명의 목적은 기존 휘발성 유기화합물(VOCs)을 대체하여 식물성 합성오일을 사용함에 따라 친환경적이면서 인체에 무해하고, 고분자를 첨가하여 방청성능이 향상된 바인더와 식물성 합성오일의 배합비를 최적화하여 이형성 및 내식성이 크게 향상된 친환경 부식방지용 이형제 제조방법을 제공함에 있다.The present invention has been made to solve the above problems, and an object of the present invention is to replace existing volatile organic compounds (VOCs) by using vegetable synthetic oil, which is environmentally friendly and harmless to the human body, and by adding a polymer to prevent rust An object of the present invention is to provide an eco-friendly anti-corrosion release agent manufacturing method with significantly improved release properties and corrosion resistance by optimizing the blending ratio of the improved binder and vegetable synthetic oil.
상기 목적을 달성하기 위한 본 발명에 따르면, 아마인유에 증류수와 계면활성제를 넣고 80℃에서 20분 동안 교반하여 현탁액을 생성하고, 생성한 80℃의 현탁액에 에폭시 수지를 넣고 20분 동안 교반하여 산화가교결합(Oxidative cross-link)을 통해 에폭시 에스테르화(Epoxy ester) 합성하여 식물성 합성오일을 수득하는 단계 및 방청제에 증류수로 희석된 촉매를 드랍하면서 3시간 동안 교반한 교반액을 생성하고, 생성한 교반액에 고분자 첨가제를 첨가하여 80℃에서 1시간 교반 후 냉각하여 바인더를 수득하는 단계 및 수득한 상기 식물성 합성오일과 상기 바인더를 3 : 7의 비율로 배합하여 이형제를 수득하는 단계를 포함하는 것을 특징으로 하는 친환경 부식방지용 이형제 제조방법이 제공된다.According to the present invention for achieving the above object, distilled water and a surfactant are added to linseed oil, stirred at 80 ° C. for 20 minutes to create a suspension, and an epoxy resin is added to the resulting suspension at 80 ° C. and stirred for 20 minutes to oxidize. Obtaining vegetable synthetic oil by synthesizing epoxy ester through oxidative cross-link and dropping a catalyst diluted with distilled water on a rust inhibitor to create an agitated solution stirred for 3 hours, Adding a polymer additive to the stirring solution, stirring at 80 ° C. for 1 hour and then cooling to obtain a binder, and mixing the obtained vegetable synthetic oil and the binder in a ratio of 3: 7 to obtain a release agent A method for manufacturing an environmentally friendly anti-corrosion release agent is provided.
여기서, 상기 방청제는 메타크릴산메틸(methyl methacrylate), N-뷰틸 아크릴레이트(butyl acrylate), 메타크릴산(methacrylic acid), 2-에틸헥실 아크릴산(2-Ethylhexyl acrylate), 트라이메틸올프로페인 트라이아크릴레이트(Trimethylolpropane triacrylate), 스티렌(styrene) 중 선택된 4종 이상이 혼합된 것을 특징으로 한다.Here, the rust inhibitor is methyl methacrylate, N-butyl acrylate, methacrylic acid, 2-ethylhexyl acrylate, trimethylolpropane tri It is characterized by a mixture of 4 or more selected from acrylate (Trimethylolpropane triacrylate) and styrene.
그리고, 상기 계면활성제는 로릴황산나트륨(Sodium Lauryl Sulfate)이고, 상기 에폭시 수지는 비스페놀 F(bisphenol F)인 것을 특징으로 한다.And, the surfactant is sodium lauryl sulfate (Sodium Lauryl Sulfate), and the epoxy resin is characterized in that bisphenol F (bisphenol F).
또한, 고분자 첨가제는 산화아연(zinc oxide), 에틸 실리케이트(ethyl silicate), 옥타메틸사이클로테트라실록산(Octamethyl Cyclotetrasiloxnae) 중 선택된 어느 하나인 것을 특징으로 한다.In addition, the polymer additive is characterized in that any one selected from zinc oxide, ethyl silicate, and octamethyl cyclotetrasiloxane.
아울러, 상기 촉매는 과황산암모늄(Ammonium Persulfate)인 것을 특징으로 한다.In addition, the catalyst is characterized in that ammonium persulfate (Ammonium Persulfate).
상기와 같은 본 발명에 의하면, 기존 휘발성 유기화합물(VOCs)을 대체하여 식물성 합성오일을 사용함에 따라 친환경적이면서 인체에 무해하여 작업장 환경을 개선할 수 있을 뿐 아니라 산업재해사고를 방지할 수 있다.According to the present invention as described above, as vegetable synthetic oil is used to replace existing volatile organic compounds (VOCs), it is environmentally friendly and harmless to the human body, thereby improving the workplace environment and preventing industrial accidents.
또한, 고분자를 첨가하여 방청성능이 향상된 바인더와 식물성 합성오일의 배합비를 최적화하여 이형성 및 내식성이 크게 향상됨에 따라 양생되는 콘크리트의 불량률이 크게 감소하여 공사비용을 현저하게 절감할 수 있다.In addition, by optimizing the blending ratio of a binder with improved anti-rust performance by adding a polymer and vegetable synthetic oil, the release property and corrosion resistance are greatly improved, so the defect rate of cured concrete is greatly reduced, and construction costs can be significantly reduced.
도 1은 본 발명의 일 실시예에 따른 친환경 부식방지용 이형제 제조방법의 공정흐름을 도시한 것.1 shows a process flow of a method for manufacturing an environmentally friendly anti-corrosion release agent according to an embodiment of the present invention.
이하에서는 도면을 참조하여 본 발명을 보다 상세하게 설명한다. 도면들 중 동일한 구성요소들은 가능한 어느 곳에서든지 동일한 부호들로 나타내고 있음에 유의해야 한다. 또한 발명의 요지를 불필요하게 흐릴 수 있는 공지기능 및 구성에 대한 상세한 설명은 생략한다.Hereinafter, the present invention will be described in more detail with reference to the drawings. It should be noted that like elements in the drawings are indicated by like reference numerals wherever possible. In addition, detailed descriptions of well-known functions and configurations that may unnecessarily obscure the subject matter of the invention will be omitted.
도 1은 본 발명의 일 실시예에 따른 친환경 부식방지용 이형제 제조방법의 공정흐름을 도시한 것이다.1 illustrates a process flow of a method for manufacturing an environmentally friendly anti-corrosion release agent according to an embodiment of the present invention.
도 1을 참조하면, 본 발명의 일 실시예에 따른 친환경 부식방지용 이형제 제조방법은 식물성 합성오일 수득 단계, 바인더 수득 단계 및 이형제 수득 단계를 포함한다.Referring to FIG. 1 , a method for manufacturing an eco-friendly anti-corrosion release agent according to an embodiment of the present invention includes a step of obtaining a vegetable synthetic oil, a step of obtaining a binder, and a step of obtaining a release agent.
식물성 합성오일 수득 단계에서는 아마인유에 증류수와 계면활성제를 넣고 80℃에서 20분 동안 교반하여 현탁액을 생성한다. 생성한 80℃의 현탁액에 에폭시 수지를 넣고 20분 동안 교반하여 산화가교결합(Oxidative cross-link)을 통해 에폭시 에스테르화(Epoxy ester) 합성하여 식물성 합성오일을 수득한다.In the step of obtaining vegetable synthetic oil, distilled water and a surfactant are added to linseed oil and stirred at 80 ° C. for 20 minutes to form a suspension. Epoxy ester was synthesized through oxidative cross-link by adding epoxy resin to the resulting suspension at 80° C. and stirring for 20 minutes to obtain vegetable synthetic oil.
여기서, 계면활성제는 로릴황산나트륨(Sodium Lauryl Sulfate)가 사용될 수 있고, 에폭시 수지는 비스페놀 F(bisphenol F)가 사용될 수 있다.Here, sodium lauryl sulfate may be used as the surfactant, and bisphenol F may be used as the epoxy resin.
위와 같이, 본 발명은 이형 기능을 갖는 물질로 종래 휘발성 유기화합물을 대체하여 식물성 오일인 아마인유를 사용함에 따라 친환경적이면서 인체에 무해하여 작업장 환경을 개선할 수 있을 뿐 아니라 산업재해사고를 방지할 수 있다.(S1)As described above, the present invention replaces the conventional volatile organic compound with a material having a release function and uses linseed oil, which is a vegetable oil, to be environmentally friendly and harmless to the human body, thereby improving the workplace environment and preventing industrial accidents. Yes (S1)
바인더 수득 단계에서는 메스실린더에 방청제를 넣고 증류수로 희석된 촉매를 스포이드로 드랍하면서 3시간 동안 교반하여 교반액을 생성한다. 생성한 교반액에 고분자 첨가제를 첨가하여 80℃에서 1시간 동안 교반 후 냉각하여 바인더를 수득한다.In the step of obtaining the binder, a rust preventive agent is put into a measuring cylinder, and the catalyst diluted with distilled water is dropped with a pipette and stirred for 3 hours to produce an agitated solution. A polymer additive is added to the resulting stirring solution, stirred at 80° C. for 1 hour, and then cooled to obtain a binder.
여기서, 방청제는 메타크릴산메틸(methyl methacrylate), N-뷰틸 아크릴레이트(butyl acrylate), 메타크릴산(methacrylic acid), 2-에틸헥실 아크릴산(2-Ethylhexyl acrylate), 트라이메틸올프로페인 트라이아크릴레이트(Trimethylolpropane triacrylate), 스티렌(styrene) 중 선택된 4종 이상을 혼합하여 사용할 수 있다.Here, the rust inhibitor is methyl methacrylate, N-butyl acrylate, methacrylic acid, 2-ethylhexyl acrylate, trimethylolpropane triacryl It can be used by mixing 4 or more types selected from trimethylolpropane triacrylate and styrene.
이러한 방청제는 교반액의 생성과정에서 선택된 4종 이상을 먼저 혼합한 후 증류수로 희석된 촉매를 드랍하면서 교반할 수도 있고, 선택된 4종 이상을 순차적으로 혼합하면서 증류수로 희석된 촉매를 드랍하면서 교반할 수도 있다.These rust inhibitors may be stirred while first mixing 4 or more selected types in the production process of the stirring solution and then drop the catalyst diluted with distilled water, or drop and stir the catalyst diluted with distilled water while mixing the selected 4 or more types sequentially. may be
촉매는 방청제와 고분자 첨가제의 반응성을 향상시키기 위해 주입되는 것으로서, 과황산암모늄(Ammonium Persulfate)가 사용될 수 있다.The catalyst is injected to improve the reactivity of the rust inhibitor and the polymer additive, and ammonium persulfate may be used.
고분자 첨가제는 방청제의 방청 성능을 향상시키기 위해 첨가되는 것으로서, 산화아연(zinc oxide), 에틸 실리케이트(ethyl silicate), 옥타메틸사이클로테트라실록산(Octamethyl Cyclotetrasiloxnae) 중 선택된 어느 하나가 사용될 수 있다.The polymer additive is added to improve the rust-preventive performance of the rust-preventive agent, and any one selected from zinc oxide, ethyl silicate, and octamethyl cyclotetrasiloxnae may be used.
위와 같이, 본 발명에 따라 수득한 바인더는 방청제에 고분자 첨가제가 첨가됨에 따라 방청 성능이 크게 향상된다.(S2)As described above, the binder obtained according to the present invention has greatly improved anti-rust performance as the polymer additive is added to the anti-rust agent. (S2)
이형제 수득 단계에서는 수득한 식물성 합성오일과 바인더를 3 : 7의 비율로 배합하여 이형제를 수득한다.(S3)In the step of obtaining a release agent, a release agent is obtained by mixing the obtained vegetable synthetic oil and binder in a ratio of 3:7. (S3)
전술한 바와 같이, 본 발명의 일 실시예에 따라 수득한 이형제는 식물성 합성오일과 고분자를 첨가하여 방청성능이 향상된 바인더를 최적화된 배합비로 배합하여 이형제를 제조함에 따라 제조되는 이형제의 이형성 및 내식성이 크게 향상된다.As described above, the release agent obtained according to one embodiment of the present invention has improved release properties and corrosion resistance of the release agent prepared by mixing a binder with improved anti-rust performance by adding vegetable synthetic oil and a polymer at an optimized mixing ratio. greatly improved
이에 따라 본 발명의 일 실시예에 따라 제조된 친환경 부식방지용 이형제를 사용하면 양생되는 콘크리트의 불량률이 크게 감소함에 따라 공사비용을 현저하게 절감할 수 있다.Accordingly, when the eco-friendly anti-corrosion release agent manufactured according to an embodiment of the present invention is used, construction costs can be remarkably reduced as the defect rate of cured concrete is greatly reduced.
이하에서는 본 발명의 일 실시예에 따라 제조된 실시예 1 내지 실시예 3과 비교예로 제시된 기존 방청이형제의 이형성 및 방청성을 확인하기 위한 항온항습시험을 실시하였다.Hereinafter, a constant temperature and humidity test was conducted to confirm the releasability and rust prevention of the existing rust-preventive release agent presented as Examples 1 to 3 and Comparative Examples prepared according to an embodiment of the present invention.
[비교예][Comparative Example]
기존 방청이형제Existing anti-corrosion agent
[실시예1][Example 1]
아마인유에 증류수와 계면활성제 성분으로 로릴황산나트륨(Sodium Lauryl Sulfate)을 넣고 80℃에서 20분 동안 교반하여 현탁액을 생성하였다.Distilled water and sodium lauryl sulfate were added to linseed oil and stirred at 80° C. for 20 minutes to form a suspension.
생성한 80℃의 현탁액에 에폭시 수지 성분으로 비스페놀 F(bisphenol F)를 넣고 20분 동안 교반하여 산화가교결합(Oxidative cross-link)을 통해 에폭시 에스테르화(Epoxy ester) 합성하여 이형제 전체 100중량% 대비 30중량%의 식물성 합성오일을 수득하였다.Add bisphenol F as an epoxy resin component to the suspension at 80 ° C and stir for 20 minutes to synthesize epoxy ester through oxidative cross-link, relative to 100% by weight of the total release agent A vegetable synthetic oil of 30% by weight was obtained.
메스 실린더에 메타크릴산메틸(methyl methacrylate) 20중량%와, N-뷰틸 아크릴레이트(butyl acrylate) 15중량%와, 메타크릴산(methacrylic acid) 10중량%와, 2-에틸헥실 아크릴산(2-Ethylhexyl acrylate) 5중량%와, 트라이메틸올프로페인 트라이아크릴레이트(Trimethylolpropane triacrylate) 5중량%와, 스티렌(styrene) 8중량%를 포함하는 방청제 63중량%를 넣고, 증류수로 희석된 촉매 과황산암모늄(Ammonium Persulfate) 5중량%를 스포이드로 드랍하면서 3시간 동안 교반하여 교반액을 생성하였다.In a measuring cylinder, 20% by weight of methyl methacrylate, 15% by weight of N-butyl acrylate, 10% by weight of methacrylic acid, and 2-ethylhexyl acrylic acid (2- Ethylhexyl acrylate) 5% by weight, trimethylolpropane triacrylate (Trimethylolpropane triacrylate) 5% by weight, styrene (styrene) 8% by weight of a rust inhibitor containing 63% by weight, Diluted catalyst ammonium persulfate with distilled water (Ammonium Persulfate) 5% by weight was dropped with a dropper and stirred for 3 hours to create a stirring solution.
생성된 교반액에 고분자 첨가제로 산화아연(zinc oxide) 2중량%를 첨가하여 80℃에서 1시간 동안 교반 후 냉각하여 이형제 전체 100중량% 대비 70중량%의 바인더를 수득하였다.2% by weight of zinc oxide as a polymer additive was added to the resulting stirring solution, stirred at 80° C. for 1 hour, and then cooled to obtain a binder of 70% by weight based on 100% by weight of the total release agent.
수득한 30중량%의 식물성 합성오일과, 70중량%의 바인더를 배합하여 친환경 부식방지용 이형제를 수득하였다.An eco-friendly anti-corrosion release agent was obtained by combining 30% by weight of the obtained vegetable synthetic oil and 70% by weight of a binder.
[실시예2][Example 2]
실시예 1과 비교하여 바인더 수득과정에서 첨가되는 고분자 첨가제가 에틸 실리케이트(ethyl silicate)로 대체되는 것이 차이가 있을 뿐, 나머지는 실시예 1과 동일하다.Compared to Example 1, the only difference is that the polymer additive added during the binder obtaining process is replaced with ethyl silicate, and the rest is the same as Example 1.
[실시예3][Example 3]
실시예 1과 비교하여 바인더 수득과정에서 첨가되는 고분자 첨가제가 옥타메틸사이클로테트라실록산(Octamethyl Cyclotetrasiloxnae)으로 대체되는 것이 차이가 있을 뿐, 나머지는 실시예 1과 동일하다.Compared to Example 1, the only difference is that the polymer additive added in the binder obtaining process is replaced with octamethyl cyclotetrasiloxane (Octamethyl Cyclotetrasiloxnae), and the rest is the same as Example 1.
비교예인 기존 방청 이형제와 본 발명의 일 실시예에 따라 제조된 실시예 1 내지 실시예 3의 친환경 부식방지용 이형제를 금속 거푸집 전면에 도포한 후, 이형제가 도포된 금속 거푸집 전면 일측에 양생 전 콘크리트 몰드를 부착하고, 온도 50℃, 습도 95%RH 환경조건에서 24시간 동안 양생한 후, 양생된 콘크리트 몰드가 제거된 금속 거푸집 전면 일측의 이형성 및 방청성을 확인하였으며, 그 결과는 하기 표1로 나타내었다.After applying the conventional rust-preventive release agent as a comparative example and the environmentally friendly anti-corrosion release agent of Examples 1 to 3 prepared according to an embodiment of the present invention on the front surface of the metal formwork, the concrete mold before curing on one side of the front surface of the metal formwork coated with the release agent was attached, and cured for 24 hours under environmental conditions of a temperature of 50 ° C and a humidity of 95% RH, and then the release property and rust prevention of one side of the front side of the metal formwork from which the cured concrete mold was removed was confirmed. The results are shown in Table 1 below. .
<표1><Table 1>
상기 표1에서 보는 바와 같이, 비교예인 기존 방청 이형제를 도포한 금속 거푸집의 경우, 일부 영역에 양생된 콘크리트 몰드 찌꺼기가 제거되지 않고 남아 있거나 녹이 발생된 것을 확인하였다.As shown in Table 1, in the case of a metal formwork coated with an existing rust-preventive mold release agent as a comparative example, it was confirmed that cured concrete mold residue was not removed or rust was generated in some areas.
반면, 본 발명의 일 실시예에 따라 제조된 친환경 부식방지 이형제를 도포한 금속 거푸집의 경우, 전체적으로 양생된 콘크리트 몰드가 깨끗하게 제거되고, 녹도 발생되지 않는 것을 확인하였다.On the other hand, in the case of a metal formwork manufactured according to an embodiment of the present invention coated with an environmentally friendly anti-corrosion release agent, it was confirmed that the cured concrete mold was removed cleanly and no rust was generated.
따라서, 본 발명의 일 실시예에 따라 제조된 친환경 부식방지 이형제가 비교예인 기존 방청 이형제에 비해 이형성 및 방청성이 우수함을 확인할 수 있었다.Therefore, it was confirmed that the anti-corrosion release agent prepared according to an embodiment of the present invention has excellent release properties and anti-rust properties compared to the conventional anti-rust release agent as a comparative example.
비록 본 발명이 상기 바람직한 실시 예들과 관련하여 설명되어졌지만, 발명의 요지와 범위로부터 벗어남이 없이 다양한 수정이나 변형을 하는 것이 가능하다. 따라서, 첨부된 특허 청구범위는 본 발명의 요지에 속하는 이러한 수정이나 변형을 포함할 것이다.Although the present invention has been described with respect to the above preferred embodiments, it is possible to make various modifications and variations without departing from the spirit and scope of the invention. Accordingly, the appended claims will cover such modifications and variations as fall within the subject matter of this invention.
Claims (5)
방청제에 증류수로 희석된 촉매를 드랍하면서 3시간 동안 교반한 교반액을 생성하고, 생성한 교반액에 고분자 첨가제를 첨가하여 80℃에서 1시간 교반 후 냉각하여 바인더를 수득하는 단계와;
수득한 상기 식물성 합성오일과 상기 바인더를 3 : 7의 비율로 배합하여 이형제를 수득하는 단계를 포함하는 것을 특징으로 하는 친환경 부식방지용 이형제 제조방법.
Add distilled water and a surfactant to linseed oil, stir at 80 ° C for 20 minutes to create a suspension, put an epoxy resin in the resulting suspension at 80 ° C and stir for 20 minutes to form an epoxy through oxidative cross-link. Obtaining vegetable synthetic oil by esterification (Epoxy ester) synthesis;
Generating a stirring solution stirred for 3 hours while dropping a catalyst diluted with distilled water on a rust inhibitor, adding a polymer additive to the resulting stirring solution, stirring at 80 ° C. for 1 hour and then cooling to obtain a binder;
An eco-friendly anti-corrosion release agent manufacturing method comprising the step of obtaining a release agent by mixing the obtained vegetable synthetic oil and the binder in a ratio of 3: 7.
상기 방청제는 메타크릴산메틸(methyl methacrylate), N-뷰틸 아크릴레이트(butyl acrylate), 메타크릴산(methacrylic acid), 2-에틸헥실 아크릴산(2-Ethylhexyl acrylate), 트라이메틸올프로페인 트라이아크릴레이트(Trimethylolpropane triacrylate), 스티렌(styrene) 중 선택된 4종 이상이 혼합된 것을 특징으로 하는 친환경 부식방지용 이형제 제조방법.
According to claim 1,
The rust inhibitor is methyl methacrylate, N-butyl acrylate, methacrylic acid, 2-ethylhexyl acrylate, trimethylolpropane triacrylate (Trimethylolpropane triacrylate), a method for manufacturing an environmentally friendly anti-corrosion release agent, characterized in that four or more selected from styrene are mixed.
상기 계면활성제는 로릴황산나트륨(Sodium Lauryl Sulfate)이고, 상기 에폭시 수지는 비스페놀 F(bisphenol F)인 것을 특징으로 하는 친환경 부식방지용 이형제 제조방법.
According to claim 1,
The surfactant is sodium lauryl sulfate, and the epoxy resin is bisphenol F.
고분자 첨가제는 산화아연(zinc oxide), 에틸 실리케이트(ethyl silicate), 옥타메틸사이클로테트라실록산(Octamethyl Cyclotetrasiloxnae) 중 선택된 어느 하나인 것을 특징으로 하는 친환경 부식방지용 이형제 제조방법.
According to claim 1,
A method for manufacturing an eco-friendly anti-corrosion release agent, characterized in that the polymer additive is any one selected from zinc oxide, ethyl silicate, and octamethyl cyclotetrasiloxane.
상기 촉매는 과황산암모늄(Ammonium Persulfate)인 것을 특징으로 하는 친환경 부식방지용 이형제 제조방법.According to claim 1,
The catalyst is an eco-friendly anti-corrosion release agent manufacturing method, characterized in that ammonium persulfate (Ammonium Persulfate).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020210180442A KR102650498B1 (en) | 2021-12-16 | 2021-12-16 | Method of manufacturing an eco-friendly anti-corrison release coating agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020210180442A KR102650498B1 (en) | 2021-12-16 | 2021-12-16 | Method of manufacturing an eco-friendly anti-corrison release coating agent |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20230091379A true KR20230091379A (en) | 2023-06-23 |
KR102650498B1 KR102650498B1 (en) | 2024-03-21 |
Family
ID=86993599
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020210180442A KR102650498B1 (en) | 2021-12-16 | 2021-12-16 | Method of manufacturing an eco-friendly anti-corrison release coating agent |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR102650498B1 (en) |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0890542A (en) * | 1994-09-28 | 1996-04-09 | Alpha Techno Co Ltd | Release agent for form |
JPH1119915A (en) * | 1997-07-07 | 1999-01-26 | Fuji Bussan Kk | Concrete releasant composition and its use method |
KR20000044421A (en) | 1998-12-30 | 2000-07-15 | 윤종용 | Method and device for minimizing battery current consumption of cellular phone |
KR20120029263A (en) * | 2010-09-16 | 2012-03-26 | 주식회사 패턴크리트 | Releasing material, manufacturing method of the same and road molding method of using the same |
KR20170060546A (en) * | 2015-11-24 | 2017-06-01 | (주)세라켐 | Aqueous separation property protective coating composition and method for manufacturing thereof and coating method by the composition and product applied by the composition |
KR102130624B1 (en) * | 2019-03-15 | 2020-07-07 | 이동희 | Preparation method of concrete release for eco-friendly water soluble agent having multiple functions |
KR102188084B1 (en) * | 2020-06-22 | 2020-12-07 | 이하민 | Composition for protecting aluminium mold with excellent adhesion and releasing property |
-
2021
- 2021-12-16 KR KR1020210180442A patent/KR102650498B1/en active IP Right Grant
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0890542A (en) * | 1994-09-28 | 1996-04-09 | Alpha Techno Co Ltd | Release agent for form |
JPH1119915A (en) * | 1997-07-07 | 1999-01-26 | Fuji Bussan Kk | Concrete releasant composition and its use method |
KR20000044421A (en) | 1998-12-30 | 2000-07-15 | 윤종용 | Method and device for minimizing battery current consumption of cellular phone |
KR20120029263A (en) * | 2010-09-16 | 2012-03-26 | 주식회사 패턴크리트 | Releasing material, manufacturing method of the same and road molding method of using the same |
KR20170060546A (en) * | 2015-11-24 | 2017-06-01 | (주)세라켐 | Aqueous separation property protective coating composition and method for manufacturing thereof and coating method by the composition and product applied by the composition |
KR102130624B1 (en) * | 2019-03-15 | 2020-07-07 | 이동희 | Preparation method of concrete release for eco-friendly water soluble agent having multiple functions |
KR102188084B1 (en) * | 2020-06-22 | 2020-12-07 | 이하민 | Composition for protecting aluminium mold with excellent adhesion and releasing property |
Also Published As
Publication number | Publication date |
---|---|
KR102650498B1 (en) | 2024-03-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2687323C (en) | Emulsion paint type damping coatings | |
CN100393828C (en) | Paint composition | |
KR100820408B1 (en) | The composition for anticorrosion Wax | |
JPH03243242A (en) | Powder die release agent for die casting | |
CN102676027B (en) | Construction method for acid-proof alkali-proof terrace | |
KR20110039734A (en) | Paint composition including nano-ceramic and polymer resin against pollution and rust of steel structure and method for surface-protection and anticorrosion using the same | |
RU2009128247A (en) | SILICA ACID AND DISPERSING AGENT FOR RETAINED CURING UNDER RADIATION, IMPROVING THE PROTECTION OF METAL SUBSTRATES FROM CORROSION | |
DE102004017221A1 (en) | O / W gel compositions with esters of pentaerythritol or its oligomers | |
KR20230091379A (en) | Method of manufacturing an eco-friendly anti-corrison release coating agent | |
KR101749306B1 (en) | The environment-friendly corrosion prevention compositions for concrete structures and constructing method using the same | |
WO2019037805A1 (en) | Joint sealant, use of the joint sealant, and method for joint sealing | |
FR2958285A1 (en) | USE OF ANTI-CORROSION AGENTS FOR THE PACKAGING OF MAGNESIUM METAL, PACKAGING MATERIAL THUS OBTAINED AND PROCESS FOR PREPARATION | |
CN1160426C (en) | Water-based metal paint | |
JP7112188B2 (en) | Anti-corrosion method for concrete structures | |
JP2018521155A (en) | Anaerobic curable composition | |
CN109789078B (en) | (meth) acrylate-based resin binder composition | |
DE102004017223A1 (en) | O / W gel compositions with waxes | |
CN108795543A (en) | A kind of engineering machinery dedicated hydraulic fluid composition | |
KR20190030913A (en) | Water-soluble stripper and anufacturing methodd thereof | |
DE3303217A1 (en) | Corrosion inhibitor based on calcined hydraulic lime | |
CN111750014A (en) | Friction lining, method for producing a friction lining and use of a friction lining | |
JP2016117040A (en) | Solidification material and solidification method of superfine powder inclusion | |
JP2021134319A (en) | Coated film-peeling agent and peeling method using coated film-peeling agent | |
JP4429687B2 (en) | Resin impregnating agent and method for producing porous body impregnated with resin impregnating agent | |
JP4545407B2 (en) | Heat resistant resin impregnating agent |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant |