[go: up one dir, main page]

KR920010097B1 - Transparent inorganic conductive coating composition - Google Patents

Transparent inorganic conductive coating composition Download PDF

Info

Publication number
KR920010097B1
KR920010097B1 KR1019890013822A KR890013822A KR920010097B1 KR 920010097 B1 KR920010097 B1 KR 920010097B1 KR 1019890013822 A KR1019890013822 A KR 1019890013822A KR 890013822 A KR890013822 A KR 890013822A KR 920010097 B1 KR920010097 B1 KR 920010097B1
Authority
KR
South Korea
Prior art keywords
coating composition
compound
conductive coating
inorganic conductive
transparent inorganic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
KR1019890013822A
Other languages
Korean (ko)
Other versions
KR910006433A (en
Inventor
손창민
Original Assignee
삼성전관 주식회사
김정배
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 삼성전관 주식회사, 김정배 filed Critical 삼성전관 주식회사
Priority to KR1019890013822A priority Critical patent/KR920010097B1/en
Publication of KR910006433A publication Critical patent/KR910006433A/en
Application granted granted Critical
Publication of KR920010097B1 publication Critical patent/KR920010097B1/en
Expired legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • H01B1/22Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
    • 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
    • C09D1/00Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/63Additives non-macromolecular organic

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Dispersion Chemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Paints Or Removers (AREA)

Abstract

내용 없음.No content.

Description

투명 무기 도전성 코팅 조성물Transparent inorganic conductive coating composition

본 발명은 투명한 무기 도전성 코팅 조성물에 관한 것이며, 특히 초미립 금속입자 및 안정제, 분산제를 사용하지 않는 투명 무기 도전성 코팅 조성물에 관한 것이다. 규소를 주원료로 하는 음극선관 및 그외 디스플레이장치는 표면에 발생하는 정전기로 인하여 인체에 악영향을 주며 먼지등이 부착되어 해상도를 저하시키게 되므로, 정전기를 제거 또는 감소시키기 위해 투명한 도전성 코팅막을 음극선관 및 디스플레이장치에 형성시켜 발생되는 정전기를 분산시키는 방식이 있는 바 도전성 조성물의 제조방법은 통상 은분등의 초미립 금속을 실리카용액에 분산시키는 방법을 채용하고 있다.The present invention relates to a transparent inorganic conductive coating composition, and more particularly, to a transparent inorganic conductive coating composition without using ultrafine metal particles, stabilizers and dispersants. Cathode ray tubes and other display devices, which are mainly made of silicon, adversely affect the human body due to static electricity generated on the surface and deteriorate the resolution by attaching dust or the like. Therefore, a transparent conductive coating film is used to remove or reduce static electricity. Since there is a method of dispersing static electricity generated by forming in the apparatus, the method for producing a conductive composition usually employs a method of dispersing ultrafine metal such as silver powder in a silica solution.

일본 공개특허공보 소화 54-110265호는 수요성규산염 화합물과 수용성 실리콘 화합불에 도전성 분말을 혼합하는 방식을 채용하고 있으며, 일본 공개특허공보 소화 63-277286호에서는 금속 알콕시드중에 금속분말을 분산시키는 방식을 취하고 있다. 또한 일본 공개특허공보 소화 63-195686호에서는 지르코늄의 옥시산염과 비침강성 실리카와 콜로이드입자를 물과 성장방지제 및 희석제에 균일하게 분산시키는 방식을 사용하고 있다.Japanese Patent Laid-Open No. 54-110265 employs a method in which conductive powder is mixed with a soluble silicate compound and a water-soluble silicone compound. Japanese Laid-Open Patent No. 63-277286 uses a method for dispersing a metal powder in a metal alkoxide. The way it is. In addition, Japanese Patent Laid-Open No. 63-195686 uses a method of uniformly dispersing zirconium oxate, non-precipitated silica, and colloidal particles in water, growth inhibitors, and diluents.

이러한 기존의 조성물의 제조는 금속분말 또는 산화물 입자를 직접 분산시키기 되어 안정제, 분산제등을 사용하여야 하므로 공정이 복잡해지고 따라서 장치 및 원료의 종류가 많아지는 단점이 있으며, 분산효과도 충분하지 않았다.In the production of such existing compositions, since the metal powder or oxide particles are directly dispersed, a stabilizer, a dispersant, or the like must be used, the process is complicated, and thus, a device and a variety of raw materials are disadvantageous, and the dispersion effect is not sufficient.

이러한 단점을 해결하기 위하여 안출해낸 본 발명의 요지는 다음과 같다. 옥시 염화 지르코늄 수화물(ZrOcl2·8H2O)등의 지르코늄 화합물에 알콜에 용해시킨 후 질산인듐(Ⅲ) 수화물(In(No3)3·xH2O) 또는 염화주석(Ⅳ) 수화물(Scnl4·xH2O)등의 인듐화합물 또는 주석화합물을 마찬가지로 알콜에 용해시켜 테트라에틸올소실리케이트(tetraethyl Orthosilicate, TEOS)와 각각 0.01~5% : 0.5~6% : 1.5~10%(부피비의 비율로 혼합한 후 수화반응을 일으켜 도전성 조성물을 만든다.The gist of the present invention devised to solve these disadvantages is as follows. Zirconium oxychloride hydrate (ZrOcl 2 · 8H 2 O) was dissolved in the alcohol to a zirconium compound such as indium nitrate (Ⅲ) hydrate (In (No 3) 3 · xH 2 O) or a tin (Ⅳ) hydrate chloride (Scnl 4 Indium or tin compounds such as xH 2 O) are dissolved in alcohol as well and mixed with tetraethyl orthosilicate (TEOS) in 0.01 ~ 5%: 0.5 ~ 6%: 1.5 ~ 10% (volume ratio) Then, a hydration reaction is performed to form a conductive composition.

이하 본 명세서에 사용되는 비율 %는 모두 부피비이다.The percentages used herein are all volume ratios.

본 발명은 기존 기술의 가진 분산 방식상의 문제를 해결하여 공정을 단순화하고 투명성과 도전성이 향상된 투명도전성 코팅조성물을 제공하는 것을 목적으로 한다.An object of the present invention is to provide a transparent conductive coating composition which simplifies the process and improves transparency and conductivity by solving the problem of the dispersion method with the existing technology.

본 발명을 실시예를 들어 상세히 설명하면 다음과 같다. 실리콘알콕시드에 알콜 및 물을 혼합하여 수화반응과 동시에 중축 반응을 일으켜 일종의 무기물 용액을 생성시킨다. 이러한 무기물 용액에 도전성 무기 코팅 조성물을 제조하는 것이다.Hereinafter, the present invention will be described in detail with reference to Examples. Alcohol and water are mixed with silicon alkoxide to cause a polycondensation reaction simultaneously with a hydration reaction to produce a kind of inorganic solution. It is to prepare a conductive inorganic coating composition in such an inorganic solution.

이러한 조성물을 얻기 위하여 본 발명은 테트라 에틸올소실리케이트(TEOS)를 약 1.5~10%를 정량한후 1차 알콜 20~50%, 2찰 알콜 0.1~8%, 3차 알콜 10~55%, 4차 알콜 15~25% 비율로 정량하여 상기 알콜 용액중에 지르코늄화합물 0.01~5%, 인듐화합물 또는 주석화합물 0.5~6%를 가한 후 혼합한다. 상기 혼합물용액에 물 5~17%를 가하여 혼합 후 상온에서 5시간 내지 30일간 동안 숙성시키면 투명 무기 도전성 코팅 조성물이 된다.In order to obtain such a composition, the present invention quantifies about 1.5 to 10% of tetraethylolsosilicate (TEOS), and then, 20 to 50% primary alcohol, 0.1 to 8% double alcohol, 10 to 55% tertiary alcohol, 4 Quantify the content of the primary alcohol at 15-25%, add 0.01-5% zirconium compound, 0.5-6% indium compound or tin compound to the alcohol solution, and mix. 5 to 17% of water is added to the mixture solution, followed by mixing at room temperature for 5 hours to 30 days to form a transparent inorganic conductive coating composition.

[실시예 1]Example 1

메탄올 100ml, 이소프로판올 60ml, 부탄올 55ml 및 t-부탄올 50ml와 테트라 에틸올소실리케이트 20ml를 혼합한 용액에 옥시 염화지르코늄 수화물 [ZrOcl2·8H2O] 0.5g과 질산인듐(Ⅲ) 수화물[In(NO3·xH2O] 10g을 가하여 혼합한 후 물 45ml를 가하여 상온에서 15일간 숙성시킨다. 이렇게 하여 생성된 본 실시예의 조성물은 기존에 비해 표면 조항이 크게 낮아져 대전방지효과가 향상되었다. (표 1참조)0.5 g of zirconium chloride hydrate [ZrOcl 2 · 8H 2 O] and indium (III) hydrate [In (NO 3) 10 g of xH 2 O] are mixed, and 45 ml of water is added thereto, followed by aging at room temperature for 15 days.The resulting composition of the present embodiment has significantly lowered the surface provisions compared with the existing ones, thereby improving the antistatic effect (see Table 1). )

[실시예 2]Example 2

테트라 에틸올소실리케이트 20ml, 메탄올 100ml 이소프로판올 60ml, 부탄올 55ml, t-부탄올 10ml을 혼합한 용액에 옥시염화 지르코늄 수화물 [ZrOcl2·8H2O] 0.5g과 염화주석(Ⅳ) 수화물[In(NO3·xH2O] 12g 가하여 혼합한 후 물 25ml를 가하여 상온에서 15일간 숙성시킨다.0.5 g of zirconium oxychloride hydrate [ZrOcl 2 · 8H 2 O] and tin (IV) hydrate [In (NO 3 ·) xH 2 O] 12g were mixed and 25ml of water were added and aged at room temperature for 15 days.

상기 각 실시예의 조성물을 음극선관의 전며에 코팅막을 형성시킨 후 표면저항을 측정하여 기존 상품과 비고하였다. 표면 저항의 특성은 측정기에 500V를 인가하여 측정한 수치이다.The composition of each example was formed on the top of the cathode ray tube and the surface resistance was measured and compared with the existing product. The surface resistance is measured by applying 500V to the measuring instrument.

[표 1]TABLE 1

Figure kpo00001
Figure kpo00001

상기 표에 도시된 바와 같이 기존제품에 비해 표면저항이 낮아져 대전방지효과가 향상 되었음을 알수 있다.As shown in the table, it can be seen that the surface resistance is lowered compared to the existing products, thereby improving the antistatic effect.

본 발명의 조성물을 사용하면 안정제, 분산제등의 참가제를 필요로 하지 않으므로 기존의 복잡한 공정을 단순화시킬 수 있음은 물론 생산원가를 낮출수 있으며, 기존의 입자 분산의 조성물에 비해 투명성이 양호하고 대전방지 또는 분산효과가 뛰어난 코팅막을 얻을 수 있는 효과가 있다.The composition of the present invention does not require a stabilizer, a dispersant, or the like, so that the existing complex process can be simplified, and the production cost can be reduced. There is an effect to obtain a coating film excellent in the prevention or dispersion effect.

Claims (4)

1차 알콜, 2차 알콜, 3차 알콜, 4차 알콜, 테트라에틸올소실리케이트의 혼합용액, 금속화합물 또는 전이금속 화합물과 물로 조성되는 것을 특징으로 하는 투명 무기 도저성 코팅 조성물.A transparent inorganic dozer coating composition comprising a primary alcohol, a secondary alcohol, a tertiary alcohol, a quaternary alcohol, a mixed solution of tetraethylolsosilicate, a metal compound or a transition metal compound and water. 제1항에 있어서, 조성물은 부피비로서 테트라에틸올소실리케이트 1.5~10%, 메탄올 20 내지 50%, 에탄올 0.1~8%, 이소프로판올 10 내지 55%, 부탄올 15 내지 25%, t-부탄올 1 내지 15%, 지르코늄화합물 0.01 내지 5%, 인듐화합물 또는 주석화합물 0.5 내지 6% 및 물 5 내지 17%로 조성되는 것을 특징으로 하는 투명 무기 도전성 코팅 조성물.The composition according to claim 1, wherein the composition has a volume ratio of tetraethylolsosilicate 1.5-10%, methanol 20-50%, ethanol 0.1-8%, isopropanol 10-55%, butanol 15-25%, t-butanol 1-15% , Zirconium compound 0.01 to 5%, indium compound or tin compound 0.5 to 6% and water transparent inorganic conductive coating composition, characterized in that 5 to 17%. 제3항에 있어서, 인듐화합물로 질산인듐(Ⅲ) 수화물 [In(NO3·xH2O] 또는 염화인듐(Ⅲ) 수화물 [In(CL3·nH2O]을 사용하는 것을 특징으로 하는 투명 무기 도전성 코팅 조성물.4. A transparent material according to claim 3, wherein an indium compound (III) hydrate [In (NO 3 · xH 2 O] or indium (III) chloride hydrate [In (CL 3 · nH 2 O]) is used as the indium compound. Inorganic conductive coating composition. 제4항에 있어서, 주석화합물로 염화주석(Ⅳ) 수화물[Sncl4·xH2O]을 사용하는 것을 특징으로 하는 투명 무기 도전성 코팅 조성물.The transparent inorganic conductive coating composition according to claim 4, wherein tin (IV) hydrate [Sncl 4 · xH 2 O] is used as the tin compound.
KR1019890013822A 1989-09-26 1989-09-26 Transparent inorganic conductive coating composition Expired KR920010097B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019890013822A KR920010097B1 (en) 1989-09-26 1989-09-26 Transparent inorganic conductive coating composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019890013822A KR920010097B1 (en) 1989-09-26 1989-09-26 Transparent inorganic conductive coating composition

Publications (2)

Publication Number Publication Date
KR910006433A KR910006433A (en) 1991-04-29
KR920010097B1 true KR920010097B1 (en) 1992-11-14

Family

ID=19290195

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019890013822A Expired KR920010097B1 (en) 1989-09-26 1989-09-26 Transparent inorganic conductive coating composition

Country Status (1)

Country Link
KR (1) KR920010097B1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100472496B1 (en) * 1997-07-23 2005-05-16 삼성에스디아이 주식회사 Transparent conductive composition, transparent conductive layer formed therefrom and manufacturing method of the transparent conductive layer

Also Published As

Publication number Publication date
KR910006433A (en) 1991-04-29

Similar Documents

Publication Publication Date Title
DE69304841T2 (en) Modified tin oxide-zirconium oxide composite sol and process for its production
Heo et al. Reaction of dehydrated Na12-A with cesium. Synthesis and crystal structure of fully dehydrated, fully cesium ion-exchanged zeolite A
DE69109222T2 (en) Body made of cerdoped quartz glass.
EP0654447B1 (en) Electro-conductive oxide particles and processes for their production
KR920010097B1 (en) Transparent inorganic conductive coating composition
Boyle et al. Synthesis and Characterization of Tris (trimethylsilyl) siloxide Derivatives of Early Transition Metal Alkoxides That Thermally Convert to Varied Ceramic–Silica Architecture Materials
JP4439876B2 (en) Chain antimony oxide fine particles, method for producing the fine particle dispersion and use thereof
US5273828A (en) Coating liquids for forming conductive coatings
US7192986B2 (en) Inorganic compound sol modified by organic compound
US7309457B2 (en) Chain inorganic oxide fine particle groups
KR0150944B1 (en) Antistatic coating composition for picture displaying screen
JPH05222562A (en) Preparation of metallic oxide sol by electrolysis
JP2014033036A (en) Paste composition for solar cell electrode
JPH0859240A (en) Titanium suboxide powder
KR100702648B1 (en) Visible light-responsive titanium dioxide colloidal solution, preparation method thereof and coating agent comprising the same
US5256484A (en) Substrate having a transparent coating thereon
JP5949395B2 (en) Production method of ITO powder
KR930003381B1 (en) Transparent antistatic coating composition
KR102841707B1 (en) Method for preparing High-transparent and High-hardness Antistatic Coating Solution and Antistatic Coating Solution prepared by the Same
JP3120663B2 (en) Conductive powder, method for producing the same, conductive dispersion and conductive paint
KR0183429B1 (en) Surface treatment liquid of glass and its manufacturing method
US5270072A (en) Coating liquids for forming conductive coatings
Kessler et al. Synthesis, crystal and molecular structure of a new heterometallic oxo-2-methoxyethoxide, BaMo2O5 (OC2H4OMe) 4 (HOC2H4OMe)
JP2628594B2 (en) Production method of glass by sol-gel method
JP2915224B2 (en) Method for producing inorganic oxide particles

Legal Events

Date Code Title Description
A201 Request for examination
PA0109 Patent application

Patent event code: PA01091R01D

Comment text: Patent Application

Patent event date: 19890926

PA0201 Request for examination

Patent event code: PA02012R01D

Patent event date: 19890926

Comment text: Request for Examination of Application

PG1501 Laying open of application
G160 Decision to publish patent application
PG1605 Publication of application before grant of patent

Comment text: Decision on Publication of Application

Patent event code: PG16051S01I

Patent event date: 19921017

E701 Decision to grant or registration of patent right
PE0701 Decision of registration

Patent event code: PE07011S01D

Comment text: Decision to Grant Registration

Patent event date: 19930130

GRNT Written decision to grant
PR0701 Registration of establishment

Comment text: Registration of Establishment

Patent event date: 19930311

Patent event code: PR07011E01D

PR1002 Payment of registration fee

Payment date: 19930311

End annual number: 3

Start annual number: 1

PR1001 Payment of annual fee

Payment date: 19951113

Start annual number: 4

End annual number: 4

PR1001 Payment of annual fee

Payment date: 19961026

Start annual number: 5

End annual number: 5

PR1001 Payment of annual fee

Payment date: 19970821

Start annual number: 6

End annual number: 6

PR1001 Payment of annual fee

Payment date: 19981028

Start annual number: 7

End annual number: 7

PR1001 Payment of annual fee

Payment date: 19991029

Start annual number: 8

End annual number: 8

PR1001 Payment of annual fee

Payment date: 20001031

Start annual number: 9

End annual number: 9

PR1001 Payment of annual fee

Payment date: 20011030

Start annual number: 10

End annual number: 10

PR1001 Payment of annual fee

Payment date: 20021030

Start annual number: 11

End annual number: 11

PR1001 Payment of annual fee

Payment date: 20031029

Start annual number: 12

End annual number: 12

PR1001 Payment of annual fee

Payment date: 20041029

Start annual number: 13

End annual number: 13

PR1001 Payment of annual fee

Payment date: 20051028

Start annual number: 14

End annual number: 14

PR1001 Payment of annual fee

Payment date: 20061027

Start annual number: 15

End annual number: 15

PR1001 Payment of annual fee

Payment date: 20071029

Start annual number: 16

End annual number: 16

FPAY Annual fee payment

Payment date: 20081029

Year of fee payment: 17

PR1001 Payment of annual fee

Payment date: 20081029

Start annual number: 17

End annual number: 17

EXPY Expiration of term
PC1801 Expiration of term