KR100362847B1 - Coating Material and Coating Method of Hot-Dip Galvanized Port Roll - Google Patents

Coating Material and Coating Method of Hot-Dip Galvanized Port Roll Download PDF

Info

Publication number
KR100362847B1
KR100362847B1 KR10-1998-0060097A KR19980060097A KR100362847B1 KR 100362847 B1 KR100362847 B1 KR 100362847B1 KR 19980060097 A KR19980060097 A KR 19980060097A KR 100362847 B1 KR100362847 B1 KR 100362847B1
Authority
KR
South Korea
Prior art keywords
coating layer
hot
post
dip galvanized
treatment
Prior art date
Application number
KR10-1998-0060097A
Other languages
Korean (ko)
Other versions
KR20000043692A (en
Inventor
조남웅
Original Assignee
주식회사 포스코
재단법인 포항산업과학연구원
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 주식회사 포스코, 재단법인 포항산업과학연구원 filed Critical 주식회사 포스코
Priority to KR10-1998-0060097A priority Critical patent/KR100362847B1/en
Publication of KR20000043692A publication Critical patent/KR20000043692A/en
Application granted granted Critical
Publication of KR100362847B1 publication Critical patent/KR100362847B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23DENAMELLING OF, OR APPLYING A VITREOUS LAYER TO, METALS
    • C23D5/00Coating with enamels or vitreous layers
    • C23D5/02Coating with enamels or vitreous layers by wet methods
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D143/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing boron, silicon, phosphorus, selenium, tellurium, or a metal; Coating compositions based on derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/003Apparatus
    • C23C2/0034Details related to elements immersed in bath
    • C23C2/00342Moving elements, e.g. pumps or mixers
    • C23C2/00344Means for moving substrates, e.g. immersed rollers or immersed bearings
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/18After-treatment

Abstract

본 발명은 세라믹 코팅층 내에 존재하는 개기공(開氣孔)을 충진하여 세라믹 코팅층의 조직을 치밀하게 하고 경도 및 내구성을 향상시키는 동시에 후처리 코팅층을 형성하여 포트 롤에 용융아연의 부착을 억제하고 스트립과의 윤활성을 향상시키는 용융아연도금 포트 롤의 코팅재 및 코팅방법을 제공하는 데 그 목적이 있다.The present invention fills the pores present in the ceramic coating layer to densify the structure of the ceramic coating layer, improve hardness and durability, and at the same time form a post-treatment coating layer to suppress the adhesion of molten zinc to the pot roll and An object of the present invention is to provide a coating material and a coating method of a hot-dip galvanized port roll which improves lubricity.

이를 실현하기 위한 본 발명은 용융아연도금 포트 롤의 세라믹 코팅층 상부를 80℃ 이상에서 건조시킨 후 상온으로 냉각하고, 이 세라믹 코팅층에, 중량 %가 Si-, Zr-, Ti-, Al-알콕사이드 : 콜로이달 실리카 : 알콜 : 물 : 촉매 : BN = 5∼30 : 0∼40 : 10∼50 : 5∼25 : 0.3∼5 : 5∼50의 비율로 조성되는 본 발명의 코팅재로 코팅하여 후처리 코팅층을 형성하고, 120∼300℃의 공기중 분위기에서 20∼60분 열처리함을 특징으로 한다.The present invention for realizing this is to dry the upper portion of the ceramic coating layer of the hot-dip galvanized pot roll at 80 ℃ or more and then cooled to room temperature, the weight percent of the ceramic coating layer, Si-, Zr-, Ti-, Al-alkoxide: Colloidal silica: alcohol: water: catalyst: BN = 5-30: 0-40: 10-50: 5-25: 0.3-5: 5-50 after coating with coating material of the present invention It is characterized in that the heat treatment for 20 to 60 minutes in an air atmosphere of 120 to 300 ℃.

Description

용융아연도금 포트 롤의 코팅재 및 코팅방법Coating Material and Coating Method of Hot-Dip Galvanized Port Roll

본 발명은 용융아연도금 포트 롤의 코팅 처리에 관한 것으로서, 보다 상세하게는 WC-Co, Al2O3를 용사 처리하여 1차로 생성된 세라믹 코팅층을 치밀하게 하고 스트립과의 윤활성을 부여하는 후처리 코팅에 사용되는 코팅재 및 코팅방법에 관한 것이다.The present invention relates to a coating treatment of a hot-dip galvanized pot roll, and more particularly, after-treatment of a ceramic coating layer formed by densely spraying WC-Co and Al 2 O 3 to give lubricity with a strip. It relates to a coating material and a coating method used for coating.

일반적으로 용융아연도금 포트는 소둔로가 있는 연속용융아연 도금 라인에서 소둔로와 쿨링 타워사이에 설치되는 것으로서, 포트 내에는 도금되는 스트립을 원활하게 지지하는 롤이 코팅액에 잠기어 있다. 이 포트 롤은 플라즈마 용사법과 후처리에 의하여 1, 2차로 코팅된다.In general, a hot dip galvanizing port is installed between an annealing furnace and a cooling tower in a continuous hot dip galvanizing line having an annealing furnace, and a roll for smoothly supporting a strip to be plated in the port is immersed in the coating liquid. This pot roll is coated first and second by plasma spraying and post-treatment.

이 플라즈마 용사법에 의한 WC-Co, Al2O3등의 세라믹 코팅층(1차 코팅)은 용사 시 프라즈마에 의해서 용융된 물질을 급냉 응고하기 때문에 조직에 기공이 발생되고, 입계 내의 균열과 같은 결함도 발생된다. 이러한 결함을 보강하기 위하여, 다공성 소결층을 크롬산 용액에 함침시켜 열처리하는 방법이 사용된다. 함침된 CrO3용액은 열처리 과정을 통하여 Cr2O3으로 상변화되면서 기공 내에 석출된다.The ceramic coating layer (primary coating) such as WC-Co and Al 2 O 3 by the plasma spray method rapidly forms and solidifies the molten material by the plasma during spraying, so that pores are generated in the structure and defects such as cracks in grain boundaries are also observed. Is generated. In order to reinforce this defect, a method of heat treatment by impregnating the porous sintered layer in the chromic acid solution is used. The impregnated CrO 3 solution is precipitated in the pores by phase change to Cr 2 O 3 through heat treatment.

또한 용융아연도금 포트 롤에 용융아연이 부착되는 것을 방지하기 위하여, 2차 코팅으로 BN 분말을 Cr2O3용액 내에 분산시켜 후처리한다. 따라서 일반적인 후처리 코팅재는 Cr2O3용액에 BN 분말을 분산한 것을 사용한다.In addition, in order to prevent hot-dip zinc from adhering to the hot-dip galvanized pot roll, BN powder is dispersed in a Cr 2 O 3 solution by a second coating and then treated. Therefore, a general post-treatment coating material uses a dispersion of BN powder in Cr 2 O 3 solution.

그러나 1차 코팅인 세라믹 코팅층의 미세 조직을 치밀하게 하기 위하여 사용되는 2차 코팅인 크롬산 용액은 강력한 산화제로 피부를 손상시켜 피부염을 일으키고, 호흡으로 흡입하면 폐암을 유발하는 등 작업자에게 직업 공해병을 발생시킬 우려가 있다.However, chromic acid solution, a secondary coating used to densify the microstructure of the ceramic coating layer, which is the primary coating, is a powerful oxidant, causing dermatitis by inhaling the skin and lung cancer when inhaled by inhalation. There is a risk of making.

따라서 본 발명은 상기와 같은 문제를 발생시키지 않으면서, 세라믹 코팅층 내에 존재하는 개기공을 충진하여 세라믹 코팅층의 조직을 치밀하게 하고 경도 및 내구성을 향상시킴과 동시에 후처리 코팅층을 형성하여 포트 롤에 용융아연의 부착을 억제하고 스트립과의 윤활성을 향상시키는 용융아연도금 포트 롤의 코팅재 및 코팅방법을 제공하는 데 그 목적이 있다.Therefore, the present invention fills the pores existing in the ceramic coating layer without causing the above problems, thereby densifying the structure of the ceramic coating layer, improving hardness and durability, and simultaneously forming a post-treatment coating layer to melt the pot roll. It is an object of the present invention to provide a coating material and a coating method of a hot dip galvanized port roll which suppresses adhesion of zinc and improves lubricity with a strip.

이를 위하여 본 발명에 따른 용융아연도금 포트 롤의 코팅재는 용융아연도금 포트 롤의 세라믹 코팅층을 후처리하는 코팅재로서, 중량 %가, 금속알콕사이드(Si-, Zr-, Ti-, Al-알콕사이드) : 콜로이달 실리카 : 알콜 : 물 : 촉매 : BN = 5∼30 : 0∼40 : 10∼50 : 5∼25 : 0.3∼5 : 5∼50의 비율로 조성됨을 특징으로 한다.To this end, the coating material of the hot-dip galvanized port roll according to the present invention is a coating material for post-treatment of the ceramic coating layer of the hot-dip galvanized port roll, and the weight% is metal alkoxide (Si-, Zr-, Ti-, Al-alkoxide): Colloidal silica: alcohol: water: catalyst: BN = 5-30: 0-40: 10-50: 5-25: 0.3-5: 5-50.

또 본 발명에 따른 용융아연도금 포트 롤의 코팅방법은 용융아연도금 포트 롤의 세라믹 코팅층 상부를 80℃ 이상에서 건조시킨 후 상온으로 냉각하여 상기 세라믹 코팅층 상부에 후처리 코팅층을 형성하는 코팅방법으로서, 중량 %가 Si-, Zr-, Ti-, Al-알콕사이드 : 콜로이달 실리카 : 알콜 : 물 : 촉매 : BN = 5∼30 : 0∼40 : 10∼50 : 5∼25 : 0.3∼5 : 5∼50의 비율로 조성되는 후처리 코팅재로 상기 후처리 코팅층을 형성할 때, 120∼300℃의 공기중 분위기에서 20∼60분 열처리함을 특징으로 한다.In addition, the coating method of the hot-dip galvanized port roll according to the present invention is a coating method of drying the upper portion of the ceramic coating layer of the hot-dip galvanizing port roll at 80 ℃ or more and cooling to room temperature to form a post-treatment coating layer on the ceramic coating layer. % By weight Si-, Zr-, Ti-, Al-alkoxide: colloidal silica: alcohol: water: catalyst: BN = 5-30: 0-40: 10-50: 5-25: 0.3-5: 5-5 When the post-treatment coating layer is formed of a post-treatment coating material formed at a ratio of 50, the heat treatment is performed for 20 to 60 minutes in an air atmosphere at 120 to 300 ° C.

이하, 본 발명을 상세히 설명한다.Hereinafter, the present invention will be described in detail.

후처리 코팅재는 금속알콕사이드(Si-, Zr-, Ti-, Al-알콕사이드), 콜로이달 실리카, 알콜, 물, 촉매, BN 분말, 분산제 등으로 제조되며, 이들은 일정 시간 교반 후 숙성하여 사용된다. 물론, 금속알콕사이드만으로도 세라믹 코팅층에 침투시켜 휘발분을 제외한 양 정도로 금속산화물을 충진할 수 있다. 그러나 이 경우 세라믹 코팅층 표면에 BN을 함유한 후처리 코팅층의 생성이 불가능하다. 기공의 충진 정도는 기공의 크기, 후처리 코팅재의 점도, 열처리 후 불휘발분의 양 등에 의하여 다르게 나타난다. 이러한 후처리 코팅재는, 먼저 금속알콕사이드(Si-, Zr-, Ti-, Al-알콕사이드), 콜로이달 실리카, 알콜, 물, 촉매 등을 원료로 하여 졸을 합성하고, 이 졸에 BN 미분말과 분산제를 사용하여 분산시킨 용액으로 제조된다.The post-treatment coating material is made of metal alkoxides (Si-, Zr-, Ti-, Al-alkoxides), colloidal silica, alcohols, water, catalysts, BN powders, dispersants and the like, which are used after aging for a certain period of time. Of course, only the metal alkoxide may penetrate the ceramic coating layer to fill the metal oxide to an amount excluding volatile matter. However, in this case, it is impossible to produce a post-treatment coating layer containing BN on the surface of the ceramic coating layer. The degree of filling of the pores is different depending on the size of the pores, the viscosity of the after-treatment coating material, the amount of nonvolatile matter after the heat treatment. This post-treatment coating material first synthesizes a sol from metal alkoxides (Si-, Zr-, Ti-, Al-alkoxides), colloidal silica, alcohols, water, catalysts, and the like, and the BN fine powder and dispersant are added to the sol. It is prepared as a solution dispersed using.

열처리는 120∼300℃의 공기중 분위기에서 20∼60분 건조한다.The heat treatment is dried for 20 to 60 minutes in an air atmosphere at 120 to 300 ℃.

후처리 코팅 및 열처리를 실시하면, 세라믹 코팅층 기공 속에 금속알콕사이드로 합성된 졸이 침투하여 기공을 충진시키고, 세라믹 코팅층 표면에는 졸을 결합제로 BN 분말이 분산되어 있는 후처리 코팅층을 형성한다. 세라믹 코팅층의 요구 경도와 후처리 코팅층의 두께에 따라 습식코팅 및 열처리를 반복적으로 실시한다.After the post-treatment coating and heat treatment, the sol synthesized with the metal alkoxide penetrates into the pores of the ceramic coating layer to fill the pores, and the post-treatment coating layer in which the BN powder is dispersed with the sol as a binder is formed on the surface of the ceramic coating layer. The wet coating and heat treatment are repeatedly performed according to the required hardness of the ceramic coating layer and the thickness of the aftertreatment coating layer.

이렇게 후처리된 코팅층은 금속알콕사이드 졸이 세라믹 코팅층의 경도를 향상시키는 동시에 후처리 코팅층 표면의 BN 분말이 스트립과의 윤활성을 증대시킨다. 또한 후처리 코팅층은 700℃ 이상의 내열성을 가지므로 도금 포트 내에서 열에 의한 손상을 적게 한다.In the post-treated coating layer, the metal alkoxide sol improves the hardness of the ceramic coating layer while the BN powder on the surface of the post-treatment coating layer increases the lubricity with the strip. In addition, the post-treatment coating layer has heat resistance of 700 ° C. or higher, thereby reducing heat damage in the plating port.

이하, 본 발명을 실시예를 통하여 구체적으로 설명한다.Hereinafter, the present invention will be described in detail through examples.

길이 90mm, 폭 40mm, 두께 3mm의 후판재를 사용하여 WC-Co를 플라즈마 용사법으로 세라믹 코팅한 시편을 제작한다. 또한 후처리 코팅재로 표 1과 같이 비교재 1∼11과 발명재 1∼11을 합성한다.Using a thick plate material having a length of 90 mm, a width of 40 mm, and a thickness of 3 mm, a specimen was prepared by ceramic coating of WC-Co by plasma spraying. In addition, Comparative Materials 1 to 11 and Inventive Materials 1 to 11 are synthesized as a post-treatment coating material.

[표 1] 후처리 코팅재의 조성 (단위 : 중량%)[Table 1] Composition of after-treatment coating material (unit: weight%)

시편Psalter 금속알콕사이드Metal alkoxide 콜로이달 실리카Colloidal silica 알콜Alcohol water 촉매catalyst BN 분말BN powder 비교재 1Comparative material 1 44 2020 3030 2020 33 2323 비교재 2Comparative material 2 3131 1010 2020 2020 33 1616 비교재 3Comparative material 3 1010 4141 1515 2020 33 1111 비교재 4Comparative material 4 1010 2020 99 2020 33 3838 비교재 5Comparative material 5 1010 1010 5151 1010 33 1616 비교재 6Comparative Material 6 1010 3030 3030 44 33 2323 비교재 7Comparative material 7 1010 3030 2020 2626 33 1111 비교재 8Comparative Material 8 1010 2020 2020 2020 0.20.2 29.0829.08 비교재 9Comparative material 9 1010 2020 2020 2020 66 2424 비교재 10Comparative Material 10 1010 3030 3030 2323 33 44 비교재 11Comparative Material 11 1010 1010 1010 1616 33 5151

시편Psalter 금속알콕사이드Metal alkoxide 콜로이달 실리카Colloidal silica 알콜Alcohol water 촉매catalyst BN 분말BN powder 발명재 1Invention 1 55 1919 3030 2020 33 2323 발명재 2Invention Material 2 3030 1111 2020 2020 33 1616 발명재 3Invention 3 1111 4040 1515 2020 33 1111 발명재 4Invention 4 1010 1919 1010 2020 33 3838 발명재 5Invention 5 1010 1111 5050 1010 33 1616 발명재 6Invention Material 6 1010 3030 2929 55 33 2323 발명재 7Invention Material 7 1010 3030 2121 2525 33 1111 발명재 8Invention Material 8 1010 2020 2020 2020 0.30.3 29.0729.07 발명재 9Invention Material 9 1010 2020 2020 2020 55 2525 발명재 10Invention Material 10 1010 3030 3030 2222 33 55 발명재 11Invention Material 11 1010 1010 1010 1717 33 5050

코팅방법은 한쪽 면에 세라믹 코팅층을 형성한 시편의 상부를 약 80℃ 이상에서 건조시킨 후 상온으로 냉각된 시편을 사용하여 표 1에 개시된 바와 같이 조성된 후처리 코팅재를 습식 코팅한다. 그리고 상온에서 후처리 코팅재를 일부 건조시킨 후, 120∼300℃ 정도의 공기중 분위기에서 20∼60분 건조시키는 열처리를 한다.In the coating method, the upper part of the specimen having the ceramic coating layer formed on one side thereof is dried at about 80 ° C. or more, and then wet coated with the post-treatment coating material as described in Table 1 using the specimen cooled to room temperature. After partially drying the post-treatment coating material at room temperature, heat treatment is performed for 20 to 60 minutes in an air atmosphere at about 120 to 300 ° C.

상온 공기중에 시편을 방치한 후, 시편의 온도가 상온 근처에서 유지되면, 재차 후처리 코팅재를 습식 코팅한 후, 상기 조건으로 열처리한다.After leaving the specimen in room temperature air, if the temperature of the specimen is maintained near room temperature, the post-treatment coating material is wet coated again, and then heat treated under the above conditions.

이러한 방법으로 후처리 코팅을 3회 실시한 결과는 표 2에 개시되어 있다.The results of three post-treatment coatings in this manner are shown in Table 2.

[표 2] 후처리 코팅층의 물성[Table 2] Physical properties of the post-treatment coating layer

시편Psalter 용액안정성Solution stability 도포성Applicability 세라믹 코팅층 경도Ceramic coating layer hardness 후처리 코팅층Post Treatment Coating Layer 윤활성Lubricity 밀착성Adhesion 비교재 1Comparative material 1 ×× ×× ×× 비교재 2Comparative material 2 ×× 비교재 3Comparative material 3 ×× ×× ×× ×× ×× 비교재 4Comparative material 4 ×× ×× 비교재 5Comparative material 5 ×× ×× ×× 비교재 6Comparative Material 6 ×× ×× ×× 비교재 7Comparative material 7 ×× ×× ×× ×× ×× 비교재 8Comparative Material 8 ×× ×× ×× 비교재 9Comparative material 9 ×× ×× ×× ×× 비교재 10Comparative Material 10 ×× 비교재 11Comparative Material 11 ×× 발명재1∼11Invention Materials 1-11

표 2에서 ○, △, ×는 각각 물성의 양호, 보통, 불량을 나타낸다.In Table 2, (circle), (triangle | delta), and (x) represent the good, normal, and poor physical property, respectively.

비교재 1, 2는 금속알콕사이드가 4, 31로, 비교재 3은 콜로이달 실리카가 41로, 비교재 4, 5는 알콜이 9, 51로, 비교재 6, 7은 물이 4, 26으로, 비교재 8, 9는 촉매가 0.2, 6으로, 그리고 비교재 10, 11은 BN 분말이 4, 51로, 각 비교재의 조성물 중 하나가 본 발명의 허용 범위를 벗어난다. 따라서 비교재 1∼11은 용액안정성과 도포성, 세라믹 코팅층 경도, 그리고 후처리 코팅층의 윤활성 및 밀착성 모두를 동시에 만족시키지는 못한다.Comparative materials 1 and 2 had metal alkoxides of 4 and 31, and comparative materials 3 had colloidal silica of 41, comparative materials 4 and 5 with alcohols 9 and 51, and comparative materials 6 and 7 with water 4 and 26. , Comparative materials 8 and 9 have catalysts of 0.2 and 6, and Comparative materials 10 and 11 have BN powders of 4 and 51, one of the compositions of each comparative material is outside the acceptable range of the present invention. Therefore, Comparative Materials 1 to 11 do not simultaneously satisfy both solution stability, applicability, ceramic coating layer hardness, and lubricity and adhesion of the aftertreatment coating layer.

그러나 발명재 1∼11은 금속알콕사이드(Si-, Zr-, Ti-, Al-알콕사이드)가 5∼30, 콜로이달 실리카가 0∼40, 알콜이 10∼50, 물이 5∼25, 촉매가 0.3∼5, 그리고 BN 분말이 5∼50으로 각각 본 발명의 허용 범위 내에 존재하기 때문에 상기와 같은 요구 물성을 모두 만족시킨다.However, the inventive materials 1 to 11 have 5 to 30 metal alkoxides (Si-, Zr-, Ti- and Al-alkoxides), 0 to 40 colloidal silica, 10 to 50 alcohols, 5 to 25 water, and 5 to 25 catalysts. Since 0.3-5 and BN powder are 5-50 each within the permissible range of this invention, all the said required physical properties are satisfy | filled.

한편, 발명재 1∼11이라 할지라도 120∼300℃ 공기중 분위기에서 20∼60분 건조시키는 열처리 이외의 조건에서는 후처리 코팅층을 형성하지 못하였다.On the other hand, even after the invention materials 1 to 11, the post-treatment coating layer could not be formed under conditions other than the heat treatment for drying for 20 to 60 minutes in an air atmosphere at 120 to 300 ° C.

상술한 바와 같이, 본 발명은 세라믹 코팅층의 기공을 금속알콕사이드로 충진하기 때문에 세라믹 코팅층의 경도 및 내구성을 향상시키는 동시에 세라믹 코팅층 표면에 BN 분말이 함유된 후처리 코팅층을 형성하기 때문에 포트 롤에 용융아연의 부착을 억제하고 스트립과의 윤활성을 향상시킬 수 있다.As described above, the present invention improves the hardness and durability of the ceramic coating layer because the pores of the ceramic coating layer are filled with metal alkoxides, and at the same time forms a post-treatment coating layer containing BN powder on the surface of the ceramic coating layer. It is possible to suppress the adhesion of and to improve the lubricity with the strip.

Claims (2)

용융아연도금 포트 롤의 세라믹 코팅층을 후처리하는 용융아연도금 포트 롤의 코팅재에 있어서,In the coating material of the hot-dip galvanized pot roll which post-processes the ceramic coating layer of the hot-dip galvanized pot roll, 중량 %가, 금속알콕사이드(Si-, Zr-, Ti-, Al-알콕사이드) : 콜로이달 실리카 : 알콜 : 물 : 촉매 : BN = 5∼30 : 0∼40 : 10∼50 : 5∼25 : 0.3∼5 : 5∼50의 비율로 조성됨을 특징으로 하는 용융아연도금 포트 롤의 코팅재.% By weight of metal alkoxide (Si-, Zr-, Ti-, Al-alkoxide): colloidal silica: alcohol: water: catalyst: BN = 5-30: 0-40: 10-50: 5-25: 0.3 -5: The coating material of the hot-dip galvanized pot roll characterized by being comprised by the ratio of 5-50. 용융아연도금 포트 롤의 세라믹 코팅층 상부를 80℃ 이상에서 건조시킨 후 상온으로 냉각하여 상기 세라믹 코팅층 상부에 후처리 코팅층을 형성하는 용융아연도금 포트 롤의 코팅방법에 있어서,In the coating method of the hot-dip galvanized port roll to dry the upper portion of the ceramic coating layer of the hot-dip galvanizing port roll after cooling to room temperature to form a post-treatment coating layer on the ceramic coating layer, 중량 %가 Si-, Zr-, Ti-, Al-알콕사이드 : 콜로이달 실리카 : 알콜 : 물 : 촉매 : BN = 5∼30 : 0∼40 : 10∼50 : 5∼25 : 0.3∼5 : 5∼50의 비율로 조성되는 후처리 코팅재로 상기 후처리 코팅층을 형성할 때, 120∼300℃의 공기중 분위기에서 20∼60분 열처리함을 특징으로 하는 용융아연도금 포트 롤의 코팅방법.% By weight Si-, Zr-, Ti-, Al-alkoxide: colloidal silica: alcohol: water: catalyst: BN = 5-30: 0-40: 10-50: 5-25: 0.3-5: 5-5 When the post-treatment coating layer is formed of a post-treatment coating material formed at a ratio of 50, the hot dip galvanized pot roll coating method, characterized in that the heat treatment for 20 to 60 minutes in an air atmosphere of 120 to 300 ℃.
KR10-1998-0060097A 1998-12-29 1998-12-29 Coating Material and Coating Method of Hot-Dip Galvanized Port Roll KR100362847B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR10-1998-0060097A KR100362847B1 (en) 1998-12-29 1998-12-29 Coating Material and Coating Method of Hot-Dip Galvanized Port Roll

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR10-1998-0060097A KR100362847B1 (en) 1998-12-29 1998-12-29 Coating Material and Coating Method of Hot-Dip Galvanized Port Roll

Publications (2)

Publication Number Publication Date
KR20000043692A KR20000043692A (en) 2000-07-15
KR100362847B1 true KR100362847B1 (en) 2003-01-24

Family

ID=19566948

Family Applications (1)

Application Number Title Priority Date Filing Date
KR10-1998-0060097A KR100362847B1 (en) 1998-12-29 1998-12-29 Coating Material and Coating Method of Hot-Dip Galvanized Port Roll

Country Status (1)

Country Link
KR (1) KR100362847B1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20010017224A (en) * 1999-08-09 2001-03-05 신현준 Sealing material and method for the thermal spray coating used in a molten metal

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101711852B1 (en) * 2009-12-29 2017-03-03 재단법인 포항산업과학연구원 Method for extending the life of ceramic roller

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6029457A (en) * 1983-07-29 1985-02-14 Nippon Steel Corp Member with high corrosion resistance immersed in hot galvanizing bath
JPH07268594A (en) * 1994-02-10 1995-10-17 Sumitomo Metal Ind Ltd Member for immersion in hot dip metal coating bath and its production
KR100273896B1 (en) * 1998-05-28 2000-12-15 박건서 Ceramic plasma spray coating method for sink roll and stabilizing roll

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6029457A (en) * 1983-07-29 1985-02-14 Nippon Steel Corp Member with high corrosion resistance immersed in hot galvanizing bath
JPH07268594A (en) * 1994-02-10 1995-10-17 Sumitomo Metal Ind Ltd Member for immersion in hot dip metal coating bath and its production
KR100273896B1 (en) * 1998-05-28 2000-12-15 박건서 Ceramic plasma spray coating method for sink roll and stabilizing roll

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20010017224A (en) * 1999-08-09 2001-03-05 신현준 Sealing material and method for the thermal spray coating used in a molten metal

Also Published As

Publication number Publication date
KR20000043692A (en) 2000-07-15

Similar Documents

Publication Publication Date Title
EP1951932B1 (en) Method of coating metal sheet
US20090297718A1 (en) Methods of fabricating environmental barrier coatings for silicon based substrates
JP2845144B2 (en) Hot-dip metal bath immersion member and method for producing the same
Conde et al. Protective properties of a sol-gel coating on zinc coated steel
US6559082B1 (en) Insulating refractory material
Jiang et al. Fabrication of barium-strontium aluminosilicate coatings on C/SiC composites via laser cladding
KR100362847B1 (en) Coating Material and Coating Method of Hot-Dip Galvanized Port Roll
JP4571250B2 (en) Roll for molten metal plating bath and method for producing the same
KR20010032153A (en) Method for Producing Member for Molten Metal Bath Having Coating Film Excellent in Resistance to Corrosion by Molten Metal
KR20000022307A (en) Member for molten metal bath provided with composite sprayed coating having excellent corrosion resistance and peeling resistance against molten metal
JP3818882B2 (en) Method for producing hydrophilic silica coating
EP0600471B1 (en) An aluminum phosphate/silicon dioxide-based sealing material
JPH0681115A (en) Member for immersion in molten metal bath subjected to pore sealing treatment with alcoholic solution of metal alkoxide
KR20110077366A (en) Method for treating surface of hearth roll and surface-treated hearth roll
JP5400194B2 (en) Molten zinc corrosion resistant metallic glass
KR20150135605A (en) Coated steel plate and mehtod for manufacturing the same
KR20150073034A (en) Anti-corrosion cold-rolled steel sheet having excellent anti-blackening property and manufacturing method thereof
JP2001131730A (en) Method for strengthening sprayed deposit, and member with strengthened sprayed deposit
JP3930653B2 (en) Roll member for aluminum-containing hot dip zinc alloy plating bath and manufacturing method thereof
JPH0610112A (en) Method for strengthening inorganic coating film
KR20010056280A (en) Galvannealing method for decreasing crater
KR20010017224A (en) Sealing material and method for the thermal spray coating used in a molten metal
JPS5819376B2 (en) Composite coating agent for centrifugal casting
KR100272298B1 (en) Pot roll for continuous hot-dip galvanizing
JPH06145936A (en) Immersion member for molten metal bath and its production

Legal Events

Date Code Title Description
A201 Request for examination
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20081028

Year of fee payment: 7

LAPS Lapse due to unpaid annual fee