KR101959815B1 - Insulating detergent composition for communication and electric equipment - Google Patents
Insulating detergent composition for communication and electric equipment Download PDFInfo
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- KR101959815B1 KR101959815B1 KR1020170151535A KR20170151535A KR101959815B1 KR 101959815 B1 KR101959815 B1 KR 101959815B1 KR 1020170151535 A KR1020170151535 A KR 1020170151535A KR 20170151535 A KR20170151535 A KR 20170151535A KR 101959815 B1 KR101959815 B1 KR 101959815B1
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- 239000000203 mixture Substances 0.000 title claims abstract description 38
- 239000003599 detergent Substances 0.000 title claims abstract description 28
- 238000004891 communication Methods 0.000 title description 4
- -1 haloalkane compound Chemical class 0.000 claims abstract description 19
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 9
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 4
- 238000009413 insulation Methods 0.000 claims description 12
- 239000003963 antioxidant agent Substances 0.000 claims description 9
- 230000003078 antioxidant effect Effects 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 238000012216 screening Methods 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 2
- 150000001348 alkyl chlorides Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 230000015556 catabolic process Effects 0.000 description 16
- 238000012360 testing method Methods 0.000 description 12
- 238000004140 cleaning Methods 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 7
- 239000012459 cleaning agent Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000000926 separation method Methods 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 238000013459 approach Methods 0.000 description 2
- 238000004925 denaturation Methods 0.000 description 2
- 230000036425 denaturation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000007257 malfunction Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000000475 sunscreen effect Effects 0.000 description 2
- 239000000516 sunscreening agent Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 1
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 241000662429 Fenerbahce Species 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- BNIXVQGCZULYKV-UHFFFAOYSA-N pentachloroethane Chemical compound ClC(Cl)C(Cl)(Cl)Cl BNIXVQGCZULYKV-UHFFFAOYSA-N 0.000 description 1
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C11D11/0047—
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/24—Hydrocarbons
- C11D7/242—Hydrocarbons branched
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/24—Hydrocarbons
- C11D7/247—Hydrocarbons aromatic
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
- C11D2111/22—Electronic devices, e.g. PCBs or semiconductors
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
Abstract
Description
본 발명은 통전기기 절연 세정제 조성물에 관한 것으로, 더 상세히는 절연성을 유지하면서도 통신전기장비 내부의 오염물을 신속하게 제거함과 동시에 세척인 및 주변 환경을 손상시키지 않는 조성물로서, 수첨 처리된 중질 나프타(hdrogen treated heavy naphtha)를 주재한 세정제 조성물에 관한 것이다.More particularly, the present invention relates to a composition for insulation detergent composition which rapidly removes contaminants in communication electric equipment while maintaining insulation, and does not deteriorate cleaning phosphorus and the surrounding environment, treated heavy naphtha.
종래 통전기기, 특히 옥외에 설치되며, 그의 내부에 회로 개폐기, 전압계, 전류계, 전력계, 적산 전력계 등이 포함되는 배전반의 내부가 먼지, 각종 이물질이 부착하여 통신, 전기의 고장, 오작동, 화재의 원인으로 되어 이를 제거하기 위한 세정제가 개발되어 판매되고 있다. 이들 절연 세정제 조성물 중, 불화암모늄, 수산화칼륨 등의 무기염류와 계면활성제를 함유하는 조성물은 먼지, 유분 등의 오염원에 대한 세정력이 떨어져 이를 사용하는 범위가 제한되고, 또한 여기에 정제유나 파라핀계 탄화수소를 배합하는 경우, 혼화성이 저하하여 장기간 보존하는 경우, 사용할 수 없는 경우에 이르게 되기도 한다. Conventional energizing devices, especially those which are installed outdoors and inside of the switchgear including circuit breakers, voltmeters, ammeters, electric power meters, integrated electric power meters, etc., are attached with dust and various foreign substances and cause communication, electric malfunction, malfunction, And a detergent for removing the detergent has been developed and sold. Among these insulating detergent compositions, inorganic salts such as ammonium fluoride, potassium hydroxide and the like and a composition containing a surfactant deteriorate the cleaning ability against pollution sources such as dust and oil, and the range of use thereof is limited. In addition, It is sometimes accompanied by a case where the compatibility is deteriorated and storage is not possible for a long period of time.
특히, 디클로로에탄, 트리클로로에탄, 펜타클로로에탄 등의 클로로알칸 화합물이 세정력이 우수하여 종래부터 세정제로 널리 이용되어 왔으나(참조, 특허문헌 1 내지 3), 최근에 이들 화합물은 피부, 목, 폐, 잔, 신장, 심지어는 암을 유발한다는 보고(Merck Index 10057, 7179, 4734 등)가 있고, 또한 각국 정부도 그의 사용을 극력 억제하고 있다. 그럼에도, 이러한 클로로알칸 화합물의 우수한 세정력 때문에 시판되는 대부분의 통전기기 절연세정제는 클로로알칸 화합물을 조성물에 대해 통상 약 20~45중량%를 배합하여 사용되고 있는 실정이다. Particularly, chloroalkane compounds such as dichloroethane, trichloroethane and pentachloroethane have been widely used as cleaners since they have excellent detergency (see
또한, 후기 특허문헌들에는 디플루오로에탄, 테트라플루오로에탄, 펜타플루오로에탄 등의 플루오로알칸 화합물을 35~90 중량부까지 배합하는 것을 제시하고 있으나, 이들 화합물은 오존층의 파괴, 주변 환경의 악화 때문에 최근 그의 사용이 제한되고 있다. 후기 특허문헌들에 이러한 기체에 액상의 파라핀계 탄화수소를 넣어 교반기를 이용하여 혼합한다고 기재되어 있으나, 이들 화합물은 플루오로알칸 화합물들은 주로 분무제(propellant)나 냉매(refrigerant)로서 사용하는 기체 화합물이며, 이러한 기체 화합물을 어떻게 배합하였는지 이해할 수 없다. 즉, 이러한 기체의 플루오로화합물의 1몰이 22.4리터인데, 이를 액화하여 사용하였다는 것인지, 또는 액상의 탄화수소에 기체의 플루오로알칸을 용해시키면서 넣었다는 것인지 이해할 수 없다. 만일 이들 플루오로알칸 화합물을 이용하여 절연세정제를 분무제로 제조하였다면, 특허문헌들에 기재된 배합비는 아마도 잘못된 것으로 보인다. Further, in the later patent documents, it has been proposed to incorporate 35 to 90 parts by weight of a fluoroalkane compound such as difluoroethane, tetrafluoroethane, pentafluoroethane or the like, but these compounds are not suitable for the destruction of the ozone layer, His use has been limited in recent years due to deterioration of his. In the later patent documents, liquid paraffinic hydrocarbons are added to these gases and mixed using a stirrer. However, these compounds are gaseous compounds which are mainly used as propellants or refrigerants, I can not understand how these gaseous compounds are compounded. That is, 22.4 liters of the fluorine compound of such a gas is 22.4 liters, and it can not be understood whether it is liquefied or used, or whether the fluoroalkane in the liquid is dissolved in the liquid hydrocarbon. If the insulating detergent is made of a spray agent using these fluoroalkane compounds, the compounding ratio disclosed in the patent literature probably seems to be wrong.
그리고, 파라핀계 탄화수소를 이용하는 경우, 파라핀계 탄화수소 단독으로 사용하는 경우, 인화점이 낮고, 절연파괴전압이 낮고, 세정력이 낮아, 할로겐화알칸 화합물을 배합하여 사용하는 것이 제시되고 있으나, 이와 같이 할로겐화알칸 화합물을 배합한 조성물은 전술한 바와 같이, 환경을 악화시키므로 바람직하지 못하다. In the case of using paraffinic hydrocarbons alone, it has been proposed to use halogenated alkane compounds in combination with low paraffinic hydrocarbons, low flash point, low dielectric breakdown voltage and low cleaning power. However, As described above, is undesirable because it deteriorates the environment.
또한, 수소 첨가 처리된 경질 정제유가 사용되기도 하나, 이러한 수소 첨가 처리 경질 정제유를 함유하는 세정제는 절연파괴전압과 인화점이 높아 세정제로서 적합하나, 세정 후 잔유물의 자연 증발 성능이 저하되는 문제점이 있는 것으로 알려져 있다. Further, although the hydrogenated refined hard refined oil is used, the refiner containing the hydrogenated refined hard refined oil is suitable as a detergent because of its high dielectric breakdown voltage and high flash point, but has a problem that the natural evaporation performance of the residue after cleaning is lowered It is known.
전술한 바와 같이, 종래의 절연 세정제 조성물은 건강 및 환경에 유해한 클로로알칸 화합물을 사용하거나, 무기염류와 계면활성제를 함유하는 조성물은 먼지, 유분 등의 오염원에 대한 세정력이 떨어지고, 또한 경질 나프타 등은 세정 후 잔유물의 자연 증발 성능이 저하되는 문제점이 있다. 본 발명은 해결하고자 하는 과제는 이러한 해결하기 위한 것이다. As described above, the conventional insulating detergent composition uses a chloroalkane compound harmful to health and environment, or a composition containing inorganic salts and a surfactant deteriorates detergency against pollution sources such as dust and oil, and hard naphtha There is a problem that the natural evaporation performance of the residue after washing is deteriorated. The problem to be solved by the present invention is to solve such a problem.
상기의 목적을 해결하기 위하여 본 발명자는 종래 사용해오던 인체 및 환경에 유해한 클로로알칸 및 환경에 유해한 플루오로알칸, 용해성이 떨어지는 무기염류, 환경을 오염시키는 계면활성제 등을 사용하지 않고, In order to solve the above-mentioned problems, the present inventors have found that the use of chloralkanes harmful to humans and the environment and fluoroalkanes harmful to the environment, inorganic salts having low solubility, surfactants that pollute the environment,
수첨 처리 중질 나프타와 이소파라핀 탄화수소; 및 수소 첨가 처리 경질 나프타로 이루어진 군에서 선택된 1종 이상을 배합하여 통전기기 절연세정제로 시험하여 본 결과, 의외로 우수한 절연파괴전압, 높은 인화점, 낮은 증기압을 나타내는 것을 발견하고, 본 발명을 완성하게 되었다. Hydrogenated heavy naphtha and isoparaffinic hydrocarbons; And hydrogenated naphtha, and found that the composition exhibits surprisingly excellent dielectric breakdown voltage, high flash point, and low vapor pressure as a result of testing with a current-carrying device insulating detergent. The present invention has been accomplished on the basis of this finding .
즉, 본 발명은 수첨 처리 중질 나프타와 이소파라핀 탄화수소 및 수첨 처리 경질 나프타로 이루어진 군에서 선택된 1종 이상을 배합하여 이루어진 통전기기 절연세정제 조성물을 제공하는 것이다. That is, the present invention is to provide an insulating composition for electrical insulating devices, comprising at least one selected from the group consisting of hydrogenated heavy naphtha, isoparaffinic hydrocarbon and hydrogenated naphtha.
또한, 본 발명은 상기 통전기기 절연세정제 조성물에 디메틸실록산을 추가로 함유하는 조성물을 제공하는 것이다. The present invention also provides a composition comprising dimethylsiloxane in the electrical insulator detergent composition.
또한, 본 발명은 상기 통전기기 절연세정제 조성물에 자외선 차단제 또는 항산화제를 추가로 함유하는 조성물을 제공하는 것이다. In addition, the present invention provides a composition containing the ultraviolet screening agent or the antioxidant in the insulating composition of the present invention.
본 발명에 의한 통전기기 절연세정제 조성물에 의하면, 통신, 전기 기기 특히 배전반 등의 외부 설치 기기의 세정력이 우수하고, 취급자 및 환경을 오염시키지 않고, 장기간 세정력을 발휘하므로 우수한 절연세정 효과를 나타낸다. INDUSTRIAL APPLICABILITY According to the insulated detergent composition for energizing device according to the present invention, excelling in the ability to clean externally installed equipment such as communication, electric equipment, especially an electric switchboard, and excellent detergent cleaning effect.
도 1은 실시예 3의 통전기기 절연 세정제 조성물의 한국전기연구원의 시험성적서 사본
도 2는 실시예 7의 통전기기 절연 세정제 조성물의 한국석유관리원의 시험성적서 사본1 is a copy of the test report of the Korea Electrotechnology Research Institute
2 is a copy of the test report of the Korean Petroleum Institute of the composition of the insulating varnish for electrification device of Example 7
본 발명은 다양한 변경을 가할 수 있고 여러 가지 실시예를 가질 수 있는바, 이하에서는 본 발명의 바람직한 형태의 실시예에서 본 발명을 상세하게 설명한다. 그러나 이는 본 발명을 예시된 실시에 의해 한정하는 것이 아니며, 본 발명의 사상 및 기술 범위는 예시된 형태의 통상적인 변경이나 균등물 내지 대체물까지 포함한다.The present invention can be variously modified and may have various embodiments. In the following, the present invention will be described in detail in the preferred embodiments of the present invention. It should be understood, however, that the invention is not to be limited by the exemplified embodiments, and that the spirit and scope of the invention encompass ordinary variations and equivalents of the illustrated forms.
본 발명 조성물에 배합되는 성분 중, 수첨 처리 중질 나프타(hydrotreated heavy naphtha, 이하, 성분 A라 한다.)란 나프타를 가압 수소 기류률 중에서 촉매 하에 수소 첨가된 나프타로서, 유기물질 등의 오염에 대한 세정제로서 알려진 Clean 420N(상품명, (주)한국하우톤제)를 사용한다. 이 Clean 420N은 인화점이 68℃로 상온에서 안전하게 배합할 수 있다. Of the components to be incorporated in the composition of the present invention, hydrotreated heavy naphtha (hereinafter referred to as component A) is a naphtha which is hydrogenated in the presence of a catalyst in a pressure hydrogen gas flow rate as a hydrogenated naphtha, Clean 420N (trade name, Korea Haiton Co., Ltd.) is used. This Clean 420N can be safely blended at room temperature with a flash point of 68 ° C.
또한, 상기 성분 A에 배합되는 성분으로서는, ISPOARAFFIN L(CAS No. 64742-48-9(상품명, 비점: 155~217℃, 밀도 0.76~0.79 kg/d㎥(15℃, 공급처: Adamas Reagent Ltd.) 및 Isopr G (상품명, Exxonmobil Chemical제, 인화점 41℃, 밀도 0.748 kg/d㎥(15℃), 비중 1.46㎟/s)으로 이루어진 군에서 선택된 1종(이하, "성분 B"라 한다.)을 배합할 수 있다. The component to be added to the component A was ISPOARAFFIN L (CAS No. 64742-48-9 (trade name, boiling point: 155 to 217 캜, density 0.76 to 0.79 kg / dm 3 (15 캜; supplied by Adamas Reagent Ltd. ) And Isopr G (trade name, manufactured by Exxonmobil Chemical, a flash point of 41 캜, a density of 0.748 kg / dm 3 (15 캜) and a specific gravity of 1.46
성분 A에 대한 성분 B의 배합비는 중량비로 60~80: 20~40의 비율로 배합하는 것이 바람직하다. 성분 A의 배합비가 60 중량부 이하이면 점도가 상승하여 취급성이 나빠지고, 세정력이 저하되며, 조성물의 혼화성이 저하하여 세정제의 균일성에 문제가 있다. 또한, A성분을 B성분에 대해 80 중량부 이상으로 배합하면, 취급성은 양호하나, 세정력이 떨어지고, 휘발성이 높아지고, 인화점이 낮아지는 등의 위험성이 있다. The blending ratio of the component B to the component A is preferably 60 to 80:20 to 40 by weight. When the blending ratio of the component A is 60 parts by weight or less, the viscosity increases and the handling property is deteriorated, the detergency is lowered, the miscibility of the composition is lowered, and the uniformity of the cleaning agent is deteriorated. If the component A is blended in an amount of 80 parts by weight or more based on the component B, the handling property is good, but the detergency is low, the volatility is high, and the flash point is low.
본 발명에서는 상기 A와 B성분에 추가로 디메틸실록산을 상기 조성물 중의 B성분에 대해 7~25중량%를 배합하면 좋다. 이러한 디메틸실록산으로서는 말단기가 히드록기로 형성(terminated)된 것으로 시판용으로는 XIAMETER(R) OHX-4010, OHX-4010, PMS-200F(한국다우코닝(주)제, CAS No. 70131-67-8), XIAMETER(R) OHX-4010(한국다우코닝(주)제XIAMETER(R) OHX-4010, (한국다우코닝(주)제), XIAMETER(R) PMS-200F(한국다우코닝(주)제) 등을 들 수 있다. 이러한 디메틸실록산을 첨가하여 관찰한 결과, 배합시, 또는 배합 후에 기포를 제거하고, 절연 세정제의 상기 성분 A와 성분 B의 혼화성, 안정성 및 내후성을 향상시키는 것을 발견하였다. 그러나 상기 범위를 초과하면 배합하면, 성분 A와 성분 B의 혼화성이 저하하고, 침전물이 생기는 것으로 보아 바람작하지 않다. In the present invention, dimethylsiloxane may be added in an amount of 7 to 25% by weight based on the B component in the composition, in addition to the components A and B described above. As such dimethylsiloxane, a terminal group is terminated by a hydroxyl group and XIAMETER (R) OHX-4010, OHX-4010, PMS-200F (CAS No. 70131-67-8 ), XIAMETER (R) OHX-4010 (XIAMETER (R) OHX-4010 manufactured by Dow Corning Incorporated (Korea), XIAMETER (R) PMS- As a result of observing the addition of dimethylsiloxane, it has been found that air bubbles are removed at the time of compounding or after compounding to improve the miscibility, stability and weatherability of the components A and B of the insulating detergent However, if it exceeds the above range, the miscibility of the component A and the component B decreases, and it is less likely to form a precipitate.
또한, 본 발명에서는 상기 A와 B성분 100 중량부에 대해 추가로 항산화제 및 자외선 차단제를 5 중량부 이하, 바람직하기로는 0.5~3.5 중량부를 첨가하여도 좋다.In the present invention, 5 parts by weight, preferably 0.5 to 3.5 parts by weight, of an antioxidant and an ultraviolet screening agent may be added to 100 parts by weight of the components A and B, respectively.
항산화제는 특히 한정되지 않으나, na-SUL BSN(KING INDUSTRIY 제) 등을 들 수 있고, 또한 자외선 차단제로서 특히 한정되지 않으나, cs123/5100(SONGSORB) 등을 들 수 있다. The antioxidant is not particularly limited, but may be exemplified by na-SUL BSN (manufactured by KING INDUSTRIY) and the like, and cs123 / 5100 (SONGSORB), although not particularly limited, as an ultraviolet screening agent.
상기 A와 B성분을 함유하는 절연세정제는 조제한 후, 즉시 사용하는 경우에는 이들 항산화제 및 자외선 차단제를 배합하지 않아도 무방하나, 장기간 보관 후에 사용하는 경우, 절연 세정제가 경시적으로 세정력이 저하할 우려가 있다. 이에 대비하여 이들 항산화제 및 자외선 차단제를 상기 범위로 첨가하여도 좋다. When the insulating detergent containing the components A and B is used, it is not necessary to blend the antioxidants and the ultraviolet screening agent when used immediately. However, when the insulating detergent is used after long-term storage, the detergent may deteriorate with time . These antioxidants and ultraviolet screening agents may be added in the above range.
이하 실시예 및 시험예를 들어 본 발명을 상세히 설명한다. Hereinafter, the present invention will be described in detail with reference to Examples and Test Examples.
우선 시험예에 대해서 설명한다. First, a test example will be described.
1. 절연과괴전압시험1. Insulation and Voltage Test
<시험방법><Test Method>
KS C IEC 60156에 따라, 시료를 용기에 채우고, 5분 후에 전압을 (2.0±0.2) kV/s의 비율로 0에서부터 일정하게 파괴가 일어날 때까지 높인다. 절연 파괴 후 최소 2분 이상, 일시 중지 간격을 두고 6회의 절연파괴를 실시한 후, 6회의 절연파괴 평균값을 kV 단위로 계산한다. According to KS C IEC 60156, the sample is filled into the vessel and after 5 minutes the voltage is raised from 0 at a rate of (2.0 ± 0.2) kV / s until constant breakdown occurs. After 6 insulation breakdowns at break intervals for at least 2 minutes after insulation breakdown, calculate the average of 6 breakdowns in kV.
<시험조건><Test Conditions>
-사용전극: 12.5mm의 황동구형 전극- Electrode used: 12.5mm brass spherical electrode
-전극의 간격: 2.50mm- Spacing of electrode: 2.50mm
-대기온도: 22.0℃- Ambient temperature: 22.0 ℃
-사료온도: 21.0℃- Feed temperature: 21.0 ℃
2. 인화점 시험2. Flash point test
<시험방법><Test Method>
KS C 2101의 12항에 따르며, 절연유의 증기에 불꽃을 가까이 대었을 때, 아래의 시험조건에서 절연유의 증기와 공기의 혼합기체가 5초 이상 연소하는 최저의 시료온도를 측정한다. According to Clause 12 of
<시험조건><Test Conditions>
-불꽃의 지름: (3~4)mm- Diameter of flame: (3 ~ 4) mm
-온도상승속도: (5~6) ℃/min- Temperature rise rate: (5 ~ 6) ℃ / min
-불꽃적용: 예상 인화점보다 (23±6)℃ 낮은 온도부터 불꽃을 접근시키고 2℃ 상승할 때마다 접근시킨다. - Flame application: approach the flame from a temperature lower than the expected flash point (23 ± 6) ℃ and approach every 2 ℃.
실시예 1Example 1
성분 A인 수첨 처리 중질 나프타(Clean 420N, (주)한국하우톤제) 60 중량부에 성분 B인 ISOPARAFFIN L(Cas No. 64742-48-9) 40 중량부를 반응기에 넣고, 상온(20℃)에서 500 rpm으로 15분간 교반하여 통전기기 절연 세정제를 얻었다. 40 parts by weight of ISOPARAFFIN L (Cas No. 64742-48-9) as component B was added to 60 parts by weight of a hydrogenated heavy naphtha (Clean 420N, Korea Hauson Co., Ltd.) as component A, and the mixture was stirred at room temperature And the mixture was stirred at 500 rpm for 15 minutes to obtain an insulated cleaner for electrification device.
얻어진 세정제의 절연파괴전압, 인화점, 증기압 (ASTM D5191-15), 수분(KS C 2101-2006)을 측정하고, 하기 표 1 및 표 2에 그 결과를 나타내었다. The breakdown voltage, flash point, vapor pressure (ASTM D5191-15) and moisture (KS C 2101-2006) of the obtained cleaning agent were measured, and the results are shown in Tables 1 and 2 below.
비교예 1Comparative Example 1
성분 A인 Clean 420N 30 중량부에 성분 B인 ISOPARAFFIN L(Cas No. 64742-48-9) L 70 중량부를 반응기에 넣고, 상온(20℃)에서 500 rpm으로 15분간 교반하여 통전기기 절연 세정제를 얻었다. 70 parts by weight of ISOPARAFFIN L (Cas No. 64742-48-9) L of Component B was added to 30 parts by weight of Clean 420N as Component A and stirred at 500 rpm for 15 minutes at room temperature (20 ° C) .
이 조성물을 24시간 보관한 후에 외관을 살펴본바, 층 분리가 일어났고, 인화점도 낮고, 또한 조성물의 점도가 높아 약간 끈적여 사용하기 불편하고, 세척력도 불량하였다. When the composition was stored for 24 hours, the appearance of the composition was observed. As a result, layer separation occurred, the flash point was low, and the viscosity of the composition was high.
실시예 2Example 2
성분 A인 Clean 420N 80 중량부에 성분 B인 Cas ISOPARAFFIN L(No. 64742-48-9) 20 중량부를 반응기에 넣고, 상온(20℃)에서 500 rpm으로 15분간 교반하여 통전기기 절연 세정제를 얻었다. 20 parts by weight of Cas ISOPARAFFIN L (No. 64742-48-9) as component B was added to 80 parts by weight of Clean 420N as Component A and stirred at 500 rpm for 15 minutes at room temperature (20 ° C) .
비교예 2Comparative Example 2
성분 A인 Clean 420N 50 중량부에 성분 B인 ISOPARAFFIN L(Cas No. 64742-48-9) L 50 중량부를 반응기에 넣고, 상온(20℃)에서 500 rpm으로 15분간 교반하여 통전기기 절연 세정제를 얻었다. 50 parts by weight of ISOPARAFFIN L (Cas No. 64742-48-9) L of Component B was added to 50 parts by weight of Clean 420N as Component A, stirred at 500 rpm at room temperature (20 ° C) for 15 minutes, .
이 조성물을 24시간 보관한 후에 외관을 살펴본바, 큰 변화는 없었으나, 세척력이 불량하고, 인화점이 낮았다. When the composition was stored for 24 hours, the appearance of the composition was not greatly changed, but the cleaning power was poor and the flash point was low.
실시예 1과 동일하게 비교예 1에서 얻어진 세정제의 절연파괴전압, 인화점, 증기압, 수분을 측정하고, 하기 표 1 및 표 2에 그 결과를 함께 나타내었다. The breakdown voltage, the flash point, the vapor pressure and the moisture of the detergent obtained in Comparative Example 1 were measured in the same manner as in Example 1, and the results are shown in Tables 1 and 2 below.
실시예 3 Example 3
실시예 1과 동일하게 하여 절연 세정제을 얻고, 이 세정제 조성물 100 중량부에 대해 na-SUL BSN 2.00 중량부를 첨가하였다. 얻어진 통전기기 절연 세정제를 60일간 보존한 후, 변성 여부와, 절연파괴전압, 인화점, 증기압, 수분을 측정하고, 이를 하기 표 1 및 표 2에 나타내었다. An insulating detergent was obtained in the same manner as in Example 1, and 2.00 parts by weight of na-SUL BSN was added to 100 parts by weight of this detergent composition. The obtained electrification device insulating detergent was stored for 60 days, and then the degree of denaturation, the breakdown voltage of the insulation, the flash point, the vapor pressure and the moisture were measured, and the results are shown in Tables 1 and 2 below.
실시예 4Example 4
실시예 1과 동일하게 하여 절연 세정제를 얻고, 이 세정제 조성물 100 중량부에 대해 cs123/5100(송원화학제) 1.5 중량부를 첨가하였다. 얻어진 통전기기 절연 세정제를 60일간 보존한 후, 변성 여부와, 절연파괴전압, 인화점, 증기압, 수분을 측정하고, 이를 하기 표 1 및 표 2에 나타내었다. An insulating detergent was obtained in the same manner as in Example 1, and 1.5 parts by weight of cs123 / 5100 (manufactured by Songwon Chemical Co., Ltd.) was added to 100 parts by weight of this detergent composition. The obtained electrification device insulating detergent was stored for 60 days, and then the degree of denaturation, the breakdown voltage of the insulation, the flash point, the vapor pressure and the moisture were measured, and the results are shown in Tables 1 and 2 below.
실시예 5Example 5
성분 A인 Clean 420N 60 중량부에 성분 B인 ISOPARAFFIN L(Cas No. 64742-48-9) 35 중량부 및 디메틸릴록산 OHX-4061(한국다우코닝제) 5중량부를 반응기에 넣고, 상온(20℃)에서 800 rpm으로 20분간 교반하여 통전기기 절연 세정제를 얻었다. 35 parts by weight of ISOPARAFFIN L (Cas No. 64742-48-9) as component B and 5 parts by weight of dimethyldiloxane OHX-4061 (manufactured by Dow Corning Toray Co., Ltd.) were added to 60 parts by weight of Clean 420N as component A, Lt; 0 > C) at 800 rpm for 20 minutes to obtain an insulated cleaning agent for electrification device.
얻어진 세정제의 절연파괴전압, 인화점, 증기압 (ASTM D5191-15), 수분(KS C 2101-2006)을 측정하고, 하기 표 1 및 표 2에 그 결과를 나타내었다. The breakdown voltage, flash point, vapor pressure (ASTM D5191-15) and moisture (KS C 2101-2006) of the obtained cleaning agent were measured, and the results are shown in Tables 1 and 2 below.
실시예 6∼10Examples 6 to 10
상기 실시예들에 준하여 하기 표 1 및 표 2에 기재된 양의 성분 A, 성분 B, 디메틸실록산, 항산화제, 자외선 차단제 등을 이용하여 통전기기 절연 세정제를 얻었다. In accordance with the above-described embodiments, an electrification device insulating cleaning agent was obtained by using the components A, B, dimethyl siloxane, antioxidant, ultraviolet ray blocking agent and the like described in the following Tables 1 and 2.
얻어진 세정제의 절연파괴전압, 인화점, 증기압 (ASTM D5191-15), 수분(KS C 2101-2006)을 측정하고, 하기 표 1 및 표 2에 그 결과를 나타내었다. The breakdown voltage, flash point, vapor pressure (ASTM D5191-15) and moisture (KS C 2101-2006) of the obtained cleaning agent were measured, and the results are shown in Tables 1 and 2 below.
상기 표 중, ○: 세척력 우수In the above table,?: Excellent cleaning power
△: 세척력 중간△: Middle washing force
×: 세척력 불량×: poor cleaning power
상기 실시예 3의 통전기기 절연 세정제 조성물을 한국전기연구원에 절연파괴시험 및 인화점 시험을 의뢰하여 측정한 바, 평균 전기절연파괴값(kV)는 79.2이었고, 인화점은 56.5℃이었다(참고: 도 1). The insulation breakdown test and the flash point test were conducted by the Korea Electrotechnology Research Institute (KEITI), and the average electrical insulation breakdown value (kV) was 79.2 and the flash point was 56.5 ° C ).
또, 실시예 7의 통전기기 절연 세정제 조성물을 한국석유관리원에 시험의뢰한 바, 인화점이 54.0℃, 수분 0.010, 증기압 7 kPa 미만이었고, 절연파괴전압은 38.8 kV이었다(참고: 도 2) In addition, when the composition of the insulated cleaning composition for electric apparatus of Example 7 was tested in Korea Petroleum Management Administration, the flash point was 54.0 ° C, the water content was 0.010, the vapor pressure was less than 7 kPa, and the insulation breakdown voltage was 38.8 kV.
Claims (6)
수첨 처리 중질 나프타 60 내지 80 중량부와
이소파라핀 탄화수소 및 수소 첨가 처리 경질 나프타로 이루어진 군에서 선택된 1종 이상 20 내지 40 중량부
를 배합함을 특징으로 하는 통전기기 절연세정제 조성물. 1. An energizing insulating detergent,
60 to 80 parts by weight of the hydrogenated heavy naphtha and
Isoparaffinic hydrocarbon and hydrogenated naphtha, 20 to 40 parts by weight of at least one member selected from the group consisting of
By weight based on the total weight of the composition.
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KR20220073218A (en) * | 2020-11-26 | 2022-06-03 | 김대환 | Detergent composition for electronic parts with good insulation properties and manufacturing method the same |
KR102474553B1 (en) * | 2022-08-26 | 2022-12-05 | 박희천 | Uninterruptible live wire cleaning agent composition for fire prevention of electrical equipment |
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KR20220073218A (en) * | 2020-11-26 | 2022-06-03 | 김대환 | Detergent composition for electronic parts with good insulation properties and manufacturing method the same |
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KR102474553B1 (en) * | 2022-08-26 | 2022-12-05 | 박희천 | Uninterruptible live wire cleaning agent composition for fire prevention of electrical equipment |
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