KR20030085271A - Electroconductive black-colored coating composition for shielding electromagnetic waves, method for forming coating film using the same and the coating film formed thereby - Google Patents

Electroconductive black-colored coating composition for shielding electromagnetic waves, method for forming coating film using the same and the coating film formed thereby Download PDF

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KR20030085271A
KR20030085271A KR1020020023621A KR20020023621A KR20030085271A KR 20030085271 A KR20030085271 A KR 20030085271A KR 1020020023621 A KR1020020023621 A KR 1020020023621A KR 20020023621 A KR20020023621 A KR 20020023621A KR 20030085271 A KR20030085271 A KR 20030085271A
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coating
conductive black
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electromagnetic wave
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KR100475549B1 (en
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손호석
김현돈
정민교
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제일모직주식회사
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    • HELECTRICITY
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Abstract

PURPOSE: A conductive black-coloring coating solution composition for screening the electromagnetic wave, a preparation method of a coating film using the composition, and a coating film prepared by the method are provided, to improve the screening efficiency for electromagnetic wave and to reduce the reflectivity and the transmittance. CONSTITUTION: The conductive black-coloring coating solution composition comprises 10-30 wt% of Ag-Au sol whose solid content is 0.9-1.4 wt%; 0.1-5 wt% of polyethylene dioxythiophene(whose solid content is 1.2-1.5 wt%) doped with polystyrene sulfonate; 0.1-0.3 wt% of an alkoxysilane; a carbon black dispersion solution whose solid content is 2-4 wt%; 5-8 wt% of an inorganic pigment mixture whose solid content is 2-4 wt%; and 60-85 wt% of an alcoholic solvent of C1-C7. Preferably the Ag-Au sol comprises the Ag microparticle coated with Au having a diameter of 10-50 nm; the alkoxysilane is tetraethoxysilane or tetramethoxysilane; and the alcoholic solvent is at least one selected from the group consisting of isopropyl alcohol, ethyl cellosolve, ethanol, propylene glycol monomethyl ether and diacetone alcohol.

Description

전자파 차폐용 도전성 블랙착색 코팅액 조성물, 그를 이용한 코팅필름의 제조방법 및 그 코팅필름{ELECTROCONDUCTIVE BLACK-COLORED COATING COMPOSITION FOR SHIELDING ELECTROMAGNETIC WAVES, METHOD FOR FORMING COATING FILM USING THE SAME AND THE COATING FILM FORMED THEREBY}ELECTROCONDUCTIVE BLACK-COLORED COATING COMPOSITION FOR SHIELDING ELECTROMAGNETIC WAVES, METHOD FOR FORMING COATING FILM USING THE SAME AND THE COATING FILM FORMED THEREBY}

본 발명은 전자파 차폐효율 및 저투과, 저반사 기능이 강화된 전자파 차폐용 도전성 블랙착색 코팅액 조성물에 관한 것으로, 보다 상세하게는 알코올 용매에 메탈졸, 전도성 고분자, 바인더 및 안료를 분산시켜 제조된 전자파 차폐용 도전성 블랙착색 코팅액 조성물, 그를 이용한 코팅필름의 제조방법 및 그 코팅필름에 관한 것이다.The present invention relates to an electroconductive black coloring coating liquid composition for electromagnetic shielding having enhanced electromagnetic shielding efficiency, low permeability, and low reflection function, and more particularly, electromagnetic waves prepared by dispersing a metal sol, a conductive polymer, a binder, and a pigment in an alcohol solvent. The conductive black coloring coating liquid composition for shielding, the manufacturing method of the coating film using the same, and its coating film are related.

전자산업의 급속한 발전과 정보소재 및 디스플레이 산업에 대한 시대적 요구에 따라 전자파간섭(EMI: electromagnetic interference)에 의한 피해가 심각한 문제로 대두되는 가운데, 이미 선진국을 중심으로 EMI에 대한 규제가 실시되기 시작하였으며 차츰 더 강화되는 추세이다.Due to the rapid development of the electronics industry and the demands of the information materials and display industries, the damage caused by electromagnetic interference (EMI) has become a serious problem, and EMI regulations have begun to be implemented mainly in developed countries. The trend is getting stronger.

음극선관(CRT: cathode ray tube)은 구동시 수많은 방사선을 발생시키는데,이러한 전자기 방사의 상당 부분은 음극선관 내의 금속 부품에 의해 차단될 수 있으나, 표시화면 밖으로 방사된 나머지 전자기장은 장시간 축적시 인체에 해로운 영향을 미치는 것으로 알려져 있다. 지금까지 이러한 문제는 표시화면의 표면에 전도성이 우수한 코팅막을 형성함으로써 해결되어 왔다.Cathode ray tubes (CRTs) generate numerous radiations when driven, and much of this electromagnetic radiation can be blocked by metal components in the cathode ray tubes, but the remaining electromagnetic fields radiated outside the display screen can cause It is known to have a harmful effect. Until now, this problem has been solved by forming a coating film having excellent conductivity on the surface of the display screen.

그러나, 기존의 곡면 모니터용으로 개발된 코팅액이 대부분 투명 도전성 용액인데 반하여, 최근 모니터의 평면화로 인해 유리 패널의 투과율이 높아지고 전자파 차폐효율 규격이 더욱 강화되면서 전도성이 우수함과 동시에 착색기능이 가미된 금속 착색 코팅액이 필요하게 되었다.However, the coating solution developed for the curved surface monitor is mostly a transparent conductive solution, whereas the recent flatness of the monitor increases the transmittance of the glass panel and further enhances the electromagnetic shielding efficiency standard, thereby providing excellent conductivity and coloring function. A coloring coating liquid was needed.

본 발명은 상기와 같은 종래기술의 문제점들을 해결하기 위한 것으로, 최근 디스플레이 시장의 변화로 더욱더 강화되고 있는 전자파차폐 규제에 대응할 수 있는 우수한 차폐효율 특성은 물론 저투과, 저반사 기능을 겸비한 도전성 블랙착색 코팅액 조성물을 제공함을 목적으로 한다.The present invention is to solve the problems of the prior art as described above, the conductive black coloration combined with excellent low-transmission, low-reflection function, as well as excellent shielding efficiency characteristics that can cope with the electromagnetic shielding regulations that are being tightened by the recent changes in the display market. It is an object to provide a coating liquid composition.

즉, 본 발명의 첫번째 측면은 다음을 포함하는 전자파 차폐용 도전성 블랙착색 코팅액 조성물을 제공한다:That is, the first aspect of the present invention provides a conductive black coloring coating liquid composition for electromagnetic wave shielding comprising:

(a) Ag-Au 졸;(a) Ag-Au sol;

(b) 폴리스티렌술포네이트(PSS)로 도프된 폴리에틸렌디옥시티오펜(PEDT);(b) polyethylenedioxythiophene (PEDT) doped with polystyrenesulfonate (PSS);

(c) 알콕시실란;(c) alkoxysilanes;

(d) 카본블랙;(d) carbon black;

(e) 무기안료; 및(e) inorganic pigments; And

(f) 탄소수 1~7개의 알코올 용매.(f) Alcohol solvents having 1 to 7 carbon atoms.

본 발명의 두번째 측면은 다음의 단계들을 포함하는 전자파 차폐용 도전성 블랙착색 코팅필름의 제조방법을 제공한다:A second aspect of the present invention provides a method of manufacturing a conductive black colored coating film for electromagnetic wave shielding, comprising the following steps:

(i) 본 발명의 전자파 차폐용 도전성 블랙착색 코팅액 조성물을 세척된 CRT 외면 유리 표면에 코팅 후 건조시켜 제 1 코팅층을 형성하는 단계;(i) coating the conductive black colored coating liquid composition for electromagnetic wave shielding of the present invention on the washed CRT outer glass surface and then drying to form a first coating layer;

(ii) 상기 제 1 코팅층 위에 2차 코팅액으로서 실리카졸을 코팅하고 건조시켜 제 2 코팅층을 형성하는 단계; 및(ii) coating and drying the silica sol as a secondary coating solution on the first coating layer to form a second coating layer; And

(iii) 상기 제 1 및 제 2 코팅층을 열소성하는 단계.(iii) thermally firing the first and second coating layers.

본 발명의 세번째 측면은 상기 방법에 의해 제조된 표면저항 102내지 103Ω/□, 투과도 60%~70%, 경도 6H~9H, 및 반사율 0.5% 이하의 특성을 갖는 전자파 차폐용 도전성 블랙착색 코팅필름을 제공한다.The third aspect of the present invention is a conductive black coloring for electromagnetic shielding having the characteristics of the surface resistance 10 2 to 10 3 Ω / □, transmittance 60% to 70%, hardness 6H to 9H, and reflectance 0.5% or less produced by the above method Provide a coating film.

이하, 본 발명의 전자파 차폐용 도전성 블랙착색 코팅액 조성물을 보다 상세하게 설명한다.Hereinafter, the electroconductive black coloring coating liquid composition for electromagnetic wave shield of this invention is demonstrated in detail.

본 발명에서는 우수한 도전성을 지닌 나노 메탈졸로서, 표면이 Au로 코팅된 Ag 미립자(입경 10~50nm)가 물과 에탄올의 혼합용매에 0.8~1.4중량%로 분산된 Ag-Au 졸을 사용한다. 이러한 Ag-Au 졸은 상업적으로 입수가능하며, 그 대표적인 예로는 스미토모 메탈 마이닝(Sumitomo Metal Mining)사의 CKR-102NH-CH1을 들 수 있다.In the present invention, as the nano-metal sol having excellent conductivity, Ag-Au sol is coated with Au particles (particle diameter 10 ~ 50nm) of 0.8 ~ 1.4% by weight in a mixed solvent of water and ethanol. Such Ag-Au sol is commercially available, and a representative example thereof is CKR-102NH-CH1 manufactured by Sumitomo Metal Mining.

본 발명의 코팅액 조성물 내 상기 Ag-Au 졸(고형분 함량 0.8~1.4중량%)의 함량은 10~30중량%이다. 본 발명의 코팅액 제조시 Ag-Au 졸을 10중량% 미만으로 사용하면 본 발명에서 목적하는 정도의 전도성(표면저항≤103Ω/□)을 얻을 수 없으며, 30중량%를 초과하여 사용하면 제조비용이 증가하여 경제성이 떨어지기 때문에 상업적으로 적합하지 않다.The content of the Ag-Au sol (solid content of 0.8 ~ 1.4% by weight) in the coating liquid composition of the present invention is 10 to 30% by weight. If the Ag-Au sol is used in less than 10% by weight in the preparation of the coating solution of the present invention, the desired degree of conductivity (surface resistance ≤ 10 3 Ω / □) cannot be obtained. It is not commercially suitable because of the increased cost and the low economic efficiency.

본 발명에서 도전성을 보완하기 위한 목적으로 사용되는 전도성 고분자는 폴리티오펜계 고분자의 일종인 수용성 폴리에틸렌디옥시티오펜(PEDT)으로, 본 발명에서는 바람직하게는 분자량이 150,000~200,000의 범위에 들고 도판트(dopant)로서 폴리스티렌술포네이트(PSS)로 도프된 PEDT를 사용하는데, 이러한 PEDT는 물에 잘 녹는 성질을 나타내며 내열성, 내습성 및 UV 안정성이 매우 우수하다는 장점을 가진다(이하, PEDT란 PSS로 도프된 PEDT를 의미함). 본 발명의 코팅액 제조시 상기 PEDT는 수용액의 형태로 첨가되는데, 이때 PEDT 수용액은 물에 대한 최적의 용해도를 유지하도록 고형분 농도가 1.2~1.5중량%로 조정되어 있다. 이러한 PEDT 수용액은 물 및/또는 알코올과 같은 유전상수가 큰 용매와 잘 혼합되기 때문에, 이러한 용매들로 희석하여 쉽게 코팅할 수 있다.The conductive polymer used for the purpose of supplementing the conductivity in the present invention is a water-soluble polyethylene dioxythiophene (PEDT) which is a kind of polythiophene-based polymer, in the present invention preferably has a molecular weight in the range of 150,000 ~ 200,000 dopant As a dopant, a PEDT doped with polystyrenesulfonate (PSS) is used, which has a property of being well soluble in water and having excellent heat resistance, moisture resistance, and UV stability (hereinafter referred to as PEDT as PSS). Mean PEDT). In preparing the coating solution of the present invention, the PEDT is added in the form of an aqueous solution, wherein the aqueous solution of the PEDT is adjusted to 1.2 to 1.5% by weight of solids so as to maintain an optimum solubility in water. Since these PEDT aqueous solutions mix well with solvents having a high dielectric constant such as water and / or alcohol, they can be easily diluted and coated with these solvents.

본 발명의 코팅액 조성물 내 상기 PEDT 수용액(고형분 함량 1.2~1.5중량%)의 함량은 0.1~5중량%이다. PEDT 수용액을 0.1중량% 미만으로 사용하면 도전성 박막 필름의 상업적으로 유용한 최소의 전도도값인 표면저항 108Ω/□를 넘게 되어 문제가 있으며, 5중량%를 초과하여 사용하는 경우에는 전도도는 우수하게 되나 PEDT와 상기 Ag-Au 졸이 코팅액 속에서 겔화를 일으키기 때문에 고균일 박막이 요구되는 음극선관 외면 유리 코팅에는 적합하지 않다.The content of the aqueous PEDT solution (solid content of 1.2 to 1.5% by weight) in the coating liquid composition of the present invention is 0.1 to 5% by weight. If the aqueous solution of PEDT is used at less than 0.1% by weight, there is a problem of exceeding the commercially available minimum conductivity value of the conductive thin film, the surface resistance of 10 8 Ω / □, when using more than 5% by weight excellent conductivity However, since the PEDT and the Ag-Au sol cause gelation in the coating solution, they are not suitable for the cathode ray tube outer glass coating requiring a high uniform thin film.

본 발명의 코팅액 조성물에는 코팅필름의 음극선관 외면 유리와의 접착성 및 막경도를 개선하기 위한 바인더로서 테트라에톡시실란(TEOS) 또는 테트라메톡시실란(TMOS)과 같은 알콕시 실란이 첨가된다. 이들은 본 발명의 코팅액 조성물 제조시 상기 PEDT 수용액에 함유된 물 또는 추가로 첨가된 물과 반응하여 가수분해반응 및 축합반응을 거쳐 실리카졸(-SiO2-SiO2-) 또는 알킬실리카졸(R-SiO2-SiO2-)을 형성한 후, PEDT와 유기-무기 하이브리드를 형성한다. 이러한 실리카졸은 그를 포함하는 코팅액 조성물을 유리 패널 위에 박막으로 코팅한 후 열경화시키면 폴리실리케이트 결정을 형성하는데, 이러한 폴리실리케이트 결정은 음극선관 외면 유리와의 접착성을 가지며, 코팅필름의 막경도를 증가시키는 역할을 하게 된다.An alkoxy silane such as tetraethoxysilane (TEOS) or tetramethoxysilane (TMOS) is added to the coating liquid composition of the present invention as a binder for improving the adhesion and film hardness of the cathode ray tube outer glass of the coating film. When the coating solution composition of the present invention is prepared, they are reacted with water or additionally added water in the aqueous solution of PEDT to undergo hydrolysis and condensation reactions, followed by silica sol (-SiO 2 -SiO 2- ) or alkylsilazole (R- After forming SiO 2 -SiO 2- ), an organic-inorganic hybrid with PEDT is formed. Such silica sol forms a polysilicate crystal when the coating liquid composition including the same is coated with a thin film on a glass panel and then thermally cured. The polysilicate crystal has adhesiveness to the outer surface of the cathode ray tube, and the film hardness of the coating film is increased. It will increase the role.

본 발명의 코팅액 조성물 내 상기 바인더의 함량은 0.1~0.3중량%이다. 바인더의 함량이 0.1중량% 미만인 경우에는 충분한 막경도(6H 이상)를 달성할 수 없는 반면, 0.3중량%를 초과하는 경우에는 막경도는 높아지나 전도성에 악영향을 주는폴리실리케이트의 양이 과다하게 되어, 별도의 전도도 향상제를 첨가하여도 본 발명의 목표인 전자파차폐 수준에 달하는 103Ω/□ 이하의 표면저항을 달성할 수 없다.The content of the binder in the coating liquid composition of the present invention is 0.1 to 0.3% by weight. When the content of the binder is less than 0.1% by weight, sufficient film hardness (more than 6H) cannot be achieved, whereas when the content of the binder is more than 0.3% by weight, the film hardness becomes high but the amount of polysilicate that adversely affects the conductivity becomes excessive. Even if a separate conductivity enhancer is added, it is not possible to achieve a surface resistance of 10 3 Ω / □ or less, which is the level of electromagnetic shielding, which is the object of the present invention.

본 발명에서는 코팅필름의 투과율 조절을 위한 안료로서 카본블랙(Carbon Black)과 아울러 질화티타늄(TiN), 코발트(Co) 및 주석(Sn) 중에서 선택되는 1종 이상의 무기안료를 병용한다. 코팅액 제조시 카본블랙과 무기안료는 각각 2~4중량%의 고형분을 포함하는 수분산액 또는 알코올 분산액 상태로 첨가되는데, 이때 상기 분산액내에 존재하는 무기안료의 입자크기는 50~150nm의 범위에 드는 것이 바람직하다.In the present invention, as a pigment for controlling the transmittance of the coating film, at least one inorganic pigment selected from carbon black (TiN), cobalt (Co), and tin (Sn) is used together. In preparing the coating solution, the carbon black and the inorganic pigment are added in the form of an aqueous dispersion or an alcohol dispersion containing 2 to 4% by weight of solids, respectively, wherein the particle size of the inorganic pigment in the dispersion falls within the range of 50 to 150 nm. desirable.

카본블랙 및 무기안료 분산액의 첨가량의 합은 전체 코팅액 조성물의 5~8중량%의 범위에 든다. 안료의 사용량이 상기 범위를 벗어나면 본 발명에서 목표로 하는 투과도(60~70%)를 달성할 수 없을 뿐만 아니라, 안료의 석출 및 얼룩 등이 발생하여 본 발명의 목적인 우수한 블랙 칼라특성을 얻을 수 없게 된다.The sum of the addition amounts of the carbon black and the inorganic pigment dispersion is in the range of 5 to 8% by weight of the total coating liquid composition. When the amount of the pigment used is out of the above range, not only the transmittance (60 to 70%) which is the target of the present invention can be achieved, but also the precipitation and staining of the pigment may occur, thereby obtaining the excellent black color characteristic of the present invention. There will be no.

본 발명에서는 상기에 열거한 성분들을 분산시키기 위한 용매로서 1종 이상의 C1~7알코올 용매를 사용하며, 바람직하게는 이소프로필 알코올(IPA), 에틸셀로솔브(EC), 에탄올(EtOH), 프로필렌 글리콜 모노메틸 에테르(PGM) 및 디아세톤 알코올(DAA)로 구성된 군에서 선택되는 1종 이상을 혼용한다.In the present invention, at least one C 1-7 alcohol solvent is used as a solvent for dispersing the above-mentioned components. Preferably, isopropyl alcohol (IPA), ethyl cellosolve (EC), ethanol (EtOH), At least one selected from the group consisting of propylene glycol monomethyl ether (PGM) and diacetone alcohol (DAA) is used in combination.

본 발명의 코팅액 조성물의 알코올 용매 함량은 전체 조성물의 60~85중량%이다. 용매 함량이 60중량% 미만이면 Ag-Au 졸 입자의 분산안정성이 저하되는 단점이 있는 반면, 85중량%를 초과하면 박막 형성시 코팅 얼룩이 발생하는 문제가 발생한다.The alcohol solvent content of the coating liquid composition of the present invention is 60 to 85% by weight of the total composition. If the solvent content is less than 60% by weight, there is a disadvantage in that the dispersion stability of the Ag-Au sol particles is lowered, whereas if the solvent content exceeds 85% by weight, a coating stain occurs when the thin film is formed.

본 발명의 코팅액 조성물을 제조하기 위해서는, 우선 소정용량의 용기에 PEDT 전도성 고분자 수용액을 첨가하고 격렬하게 교반하면서, 알코올 용매, 알콕시 실란, 및 술폰산 모노머 도판트를 순차적으로 첨가하고, 상온에서 3시간 정도 교반한다. 이렇게 제조된 중간용액에 수분산 카본블랙 및 무기안료를 첨가하고 약 4시간 정도 교반한다. 그런 다음, 최종적으로 Ag-Au 졸을 첨가하고 충분히 교반하면 코팅액이 완성된다. 코팅액 완성후에는 이물 제거를 위해 10.0 마이크론 필터를 이용하여 필터링을 실시하는 것이 좋다. 나노 메탈졸 코팅액의 필터링시 10.0 마이크론 이하의 세공을 가진 필터를 사용하면 순간적으로 필터 표면에서 응집(flocculation)이 발생할 수 있어 바람직하지 못하다. 또한, 가능한한 별도의 압력을 가하지 않고 자중으로 코팅액이 필터를 통과할 수 있도록 하는 것이 좋다.In order to prepare the coating liquid composition of the present invention, first, an aqueous solution of PEDT conductive polymer is added to a container having a predetermined capacity, followed by vigorous stirring, and then an alcohol solvent, an alkoxy silane, and a sulfonic acid monomer dopant are sequentially added, and about 3 hours at room temperature. Stir. The aqueous dispersion carbon black and the inorganic pigment are added to the intermediate solution thus prepared and stirred for about 4 hours. Then, Ag-Au sol is finally added and stirred sufficiently to complete the coating solution. After the coating solution is completed, it is recommended to filter using a 10.0 micron filter to remove foreign substances. 10.0 when filtering nano metal sol coating solution The use of filters with sub-micron pores is undesirable because it can cause flocculation on the filter surface in an instant. In addition, it is good to allow the coating liquid to pass through the filter at its own weight without applying additional pressure as much as possible.

이하, 본 발명의 전자파 차폐용 도전성 블랙착색 코팅액 조성물을 사용하여 음극선관(CRT) 외면 유리에 코팅필름을 형성하는 방법을 단계별로 나누어 설명하면 다음과 같다:Hereinafter, a method of forming a coating film on a cathode ray tube (CRT) outer surface glass using the conductive black coloring coating liquid composition for electromagnetic wave shielding according to the present invention will be described as follows.

i) CRT 외면 유리를 CeO2로 폴리싱(polishing)한 후, 에탄올로 세척하고 건조시킨다.i) The CRT outer glass is polished with CeO 2 , then washed with ethanol and dried.

ii) 상술한 바와 같이 제조된 본 발명의 코팅액 조성물을 상기 i) 단계에서 세척된 CRT 외면 유리 표면에 스핀 코팅 또는 스프레이 코팅하고 70~80초간 건조시켜 제 1 코팅층을 형성시킨다. 스핀 코팅시 회전속도는 80~150rpm이 적당하고, 시간은 50~80초가 적당하다.ii) spin coating or spray coating the coating liquid composition of the present invention prepared as described above on the CRT outer glass surface washed in step i) and dried for 70 to 80 seconds to form a first coating layer. When spin coating, the proper rotation speed is 80 ~ 150rpm and the time is 50 ~ 80 seconds.

iii) 상기 제 1 코팅층 위에 후술하는 2차 코팅액을 스핀 코팅 또는 스프레이 코팅하고 70~80초간 건조시켜 제 2 코팅층을 형성시킨다. 1차 코팅과 마찬가지로, 스핀 코팅시 회전속도는 80~150rpm이 적당하고, 시간은 50~80초가 적당하다.iii) spin coating or spray coating a secondary coating solution described later on the first coating layer and drying for 70 to 80 seconds to form a second coating layer. As in the primary coating, the spin speed is appropriately 80 to 150 rpm, and the time is 50 to 80 seconds.

iv) 마지막으로 180~200℃에서 60~90분 동안 소성하여 도전성 블랙착색 코팅필름을 수득한다.iv) Finally, firing at 180-200 ° C. for 60-90 minutes yields a conductive black colored coating film.

상기에서 2차 코팅액이라 함은 분자량(Mw)이 1200 내지 1500인 실리카졸로서, 코팅층의 저반사 특성과 막경도를 보완해주는 역할을 한다. 이러한 2차 코팅액을 얻기 위해서는 A, B, C 3가지 예비용액이 필요한데, A 용액은 에탄올과 메틸실리케이트를 약 10분간 교반 혼합하여 제조되고, B 용액은 에탄올과 증류수를 약 10분간 교반 혼합하여 제조되며, C 용액은 에탄올과 질산, 염산 또는 황산 촉매를 약 10분간 교반 혼합하여 제조된다. 이와 같이 3가지 예비용액이 모두 제조되면, 먼저 A 용액에 B 용액을 첨가한 뒤 10분간 교반하고, 여기에 C용액을 첨가하여 15분간 더 교반한다. 그런 다음, 이소프로필알코올, 증류수, 1-부탄올 및 에틸셀로솔브를 소정량 첨가하고 교반하면 2차 코팅액이 완성된다. 완성된 코팅액은 사용전에 1.0 마이크론 필터로 필터링한 후 GPC(gel permeation chromatography)를 이용하여 분자량을 측정한다. 기존의 ITO 또는 ATO 코팅의 경우 2차 코팅액의 중량평균분자량(Mw)은 약 3000~3500 정도이었지만, 1차 코팅액으로서 본 발명에 의한 코팅액 조성물을 사용하는 경우에는 낮은 표면저항과 반사율 특성을 고려하여 2차 코팅액의 분자량(Mw)이 1500 이하로 관리되어야 된다.The secondary coating solution is a silica sol having a molecular weight (Mw) of 1200 to 1500, and serves to complement the low reflection characteristics and film hardness of the coating layer. In order to obtain such a secondary coating solution, A, B, and C preliminary solutions are required. A solution is prepared by stirring and mixing ethanol and methyl silicate for about 10 minutes, and B solution is prepared by stirring and mixing ethanol and distilled water for about 10 minutes. C solution is prepared by stirring and mixing ethanol and nitric acid, hydrochloric acid or sulfuric acid catalyst for about 10 minutes. When all three preliminary solutions are prepared as described above, first, after adding the B solution to the A solution, the solution is stirred for 10 minutes, and the C solution is added thereto, followed by further stirring for 15 minutes. Then, a predetermined amount of isopropyl alcohol, distilled water, 1-butanol and ethyl cellosolve is added and stirred to complete the secondary coating solution. The finished coating solution is filtered with a 1.0 micron filter before use and then the molecular weight is measured by gel permeation chromatography (GPC). In the case of conventional ITO or ATO coating, the weight average molecular weight (Mw) of the secondary coating solution was about 3000 to 3500, but in the case of using the coating solution composition according to the present invention as the primary coating solution in consideration of low surface resistance and reflectance characteristics The molecular weight (Mw) of the secondary coating solution should be controlled to 1500 or less.

이상과 같이 제조된 본 발명의 코팅필름은 표면저항이 102내지 103Ω/□, 투과도가 60%~70%, 경도가 6H~9H, 그리고 반사율이 0.5% 이하인 특성을 갖는다.The coating film of the present invention prepared as described above has a surface resistance of 10 2 to 10 3 Ω / □, transmittance of 60% to 70%, hardness of 6H ~ 9H, and reflectance of 0.5% or less.

이하, 실시예를 통하여 본 발명을 보다 구체적으로 설명하고자 하나, 이러한 실시예들은 단지 설명의 목적을 위한 것으로 본 발명을 제한하는 것으로 해석되어서는 안된다.Hereinafter, the present invention will be described in more detail with reference to examples, but these examples are for illustrative purposes only and should not be construed as limiting the present invention.

제조예 1~4: 1차 코팅액의 제조Preparation Examples 1-4: Preparation of Primary Coating Liquid

하기 표 1에 기재된 조성에 따라, 소정용량의 용기에 먼저 PEDT 전도성 고분자 수용액(1.3중량%)을 첨가하고 격렬하게 교반하면서, 알코올 용매, 바인더로서 테트라에톡시실란, 및 도판트로서 술폰산을 순차적으로 첨가하고, 상온에서 3시간동안 교반하여 중간용액을 얻었다. 상기 중간용액에 수분산 카본블랙 및 무기안료로서 TiN(2중량%, aq.)을 첨가하고, 4시간 동안 교반하였다. 그런 다음, Ag-Au 졸(1.4중량%)을 첨가하고, 3시간 동안 교반한 후 10.0 마이크론 필터로 필터링하여 코팅액 조성물을 완성하였다.According to the composition shown in Table 1 below, an aqueous solution of PEDT conductive polymer (1.3% by weight) was first added to a container of a predetermined capacity, followed by vigorous stirring, followed by sequentially adding an alcohol solvent, tetraethoxysilane as a binder, and sulfonic acid as a dopant. The mixture was added and stirred at room temperature for 3 hours to obtain an intermediate solution. To the intermediate solution, TiN (2% by weight, aq.) Was added as a water-dispersible carbon black and an inorganic pigment, and stirred for 4 hours. Ag-Au sol (1.4 wt%) was then added, stirred for 3 hours and filtered with a 10.0 micron filter to complete the coating solution composition.

상기에서, Ag-Au 졸과 TiN으로는 각각 스미토모 메탈마이닝(SUMITOMO METAL MINING)사의 CKR-102NH-CH1(1.4중량%)과 TPD-N(2중량%, aq.)을 필터링하여 사용하였고, PEDT 전도성 고분자 수용액으로는 베이어(BAYER)사의 Baytron PH를 사용하였으며, 수분산 카본블랙으로는 미츠비시 머티리얼(Mitsubishi Materails)사의 평균입경 110nm인 카본블랙을 사용하였다.In the above, Ag-Au sol and TiN were used by filtering CKR-102NH-CH1 (1.4 wt%) and TPD-N (2 wt%, aq.) Of Sumitomo Metal Mining Co., Ltd., respectively, and PEDT. Baytron PH of BAYER was used as the conductive polymer solution, and carbon black having an average particle diameter of 110 nm was used as Mitsubishi Materails.

구분division 조성Furtherance 제조예 1Preparation Example 1 PEDT(1.3wt%, aq) 0.2wt%IPA 3wt%EC 3wt%EtOH 52.2wt%PGM 5wt%DAA 3wt%Ag-Au(1.4wt%) 27wt%TiN(2wt%, aq) 6wt%카본블랙 0.5wt%테트라에톡시실란 0.1wt%PEDT (1.3wt%, aq) 0.2wt% IPA 3wt% EC 3wt% EtOH 52.2wt% PGM 5wt% DAA 3wt% Ag-Au (1.4wt%) 27wt% TiN (2wt%, aq) 6wt% Carbon Black 0.5wt Tetraethoxysilane 0.1 wt% 제조예 2Preparation Example 2 PEDT(1.3wt%, aq) 0.5wt%IPA 3wt%EC 3wt%EtOH 51.9wt%PGM 5wt%DAA 3wt%Ag-Au(1.4wt%) 27wt%TiN(2wt%, aq) 6wt%카본블랙 0.5wt%테트라에톡시실란 0.1wt%PEDT (1.3wt%, aq) 0.5wt% IPA 3wt% EC 3wt% EtOH 51.9wt% PGM 5wt% DAA 3wt% Ag-Au (1.4wt%) 27wt% TiN (2wt%, aq) 6wt% Carbon Black 0.5wt Tetraethoxysilane 0.1 wt% 제조예 3Preparation Example 3 PEDT(1.3wt%, aq) 1.0wt%IPA 3wt%EC 3wt%EtOH 51.4wt%PGM 5wt%DAA 3wt%Ag-Au(1.4wt%) 27wt%TiN(2wt%, aq) 6wt%카본블랙 0.5wt%테트라에톡시실란 0.1wt%PEDT (1.3wt%, aq) 1.0wt% IPA 3wt% EC 3wt% EtOH 51.4wt% PGM 5wt% DAA 3wt% Ag-Au (1.4wt%) 27wt% TiN (2wt%, aq) 6wt% Carbon Black 0.5wt Tetraethoxysilane 0.1 wt% 제조예 4Preparation Example 4 PEDT(1.3wt%, aq) 1.5wt%IPA 3wt%EC 3wt%EtOH 50.9wt%PGM 5wt%DAA 3wt%Ag-Au(1.4wt%) 27wt%TiN(2wt%, aq) 6wt%카본블랙 0.5wt%테트라에톡시실란 0.1wt%PEDT (1.3wt%, aq) 1.5wt% IPA 3wt% EC 3wt% EtOH 50.9wt% PGM 5wt% DAA 3wt% Ag-Au (1.4wt%) 27wt% TiN (2wt%, aq) 6wt% Carbon Black 0.5wt Tetraethoxysilane 0.1 wt%

주) IPA : Isopropylalcohol(이소프로필알코올)IPA: Isopropylalcohol (isopropyl alcohol)

EC : Ethyl cellosolve(에틸셀로솔브)EC: Ethyl cellosolve

DAA : Diacetonealcohol(디아세톤알코올)DAA: Diacetone alcohol (diacetone alcohol)

PGM : Propyleneglycol monomethyl ether(프로필렌글리콜 모노메틸에테르)PGM: Propyleneglycol monomethyl ether

제조예 5-6: 2차 코팅액의 제조Preparation Example 5-6 Preparation of Secondary Coating Liquid

먼저 250g의 에탄올과 150g의 메틸실리케이트를 10분 정도 교반 혼합하여 용액 A를 제조하고, 150g의 에탄올과 115g의 증류수를 약 10분간 교반 혼합하여 용액 B를 제조하였으며, 46g의 에탄올과 소량의 질산촉매를 약 10분간 교반 혼합하여 용액 C를 제조하였다. 그런 다음, 상기 A 용액에 B 용액을 첨가한 뒤 10분간 교반하고, 여기에 C 용액을 첨가한 후 15분간 더 교반하여 농축 실리카졸을 얻었다. 이와 같이 제조된 농축 실리카졸에 하기 표 2의 조성에 따라 이소프로필알코올, 증류수, 1-부탄올 및 에틸셀로솔브를 첨가하여 희석한 후, 1.0 마이크론 필터로 필터링하여 2차 코팅액을 완성하였다. 완성된 2차 코팅액의 분자량을 워터(WATER)사의 Styragel(7.8mm diameter) 칼럼과 용제로서 테트라하이드로퓨란(THF)을 사용하여 측정하였으며, 그 결과는 하기 표 2와 같다.First, Solution A was prepared by stirring and mixing 250 g of ethanol and 150 g of methyl silicate for about 10 minutes. Then, Solution B was prepared by stirring and mixing 150 g of ethanol and 115 g of distilled water for about 10 minutes, and 46 g of ethanol and a small amount of nitric acid catalyst. The solution C was prepared by stirring and mixing for about 10 minutes. Then, the solution B was added to the solution A, followed by stirring for 10 minutes, and solution C was added thereto, followed by further stirring for 15 minutes to obtain a concentrated silica sol. Thus prepared isopropyl alcohol, distilled water, 1-butanol and ethyl cellosolve were diluted according to the composition shown in Table 2, and then diluted with a 1.0 micron filter to complete the secondary coating solution. The molecular weight of the finished secondary coating solution was measured using a Styragel (7.8 mm diameter) column of WATER company and tetrahydrofuran (THF) as a solvent, the results are shown in Table 2 below.

구분division 제조예 5Preparation Example 5 제조예 6Preparation Example 6 조성Furtherance 농축 실리카졸 9wt%IPA 58wt%증류수 3wt%1-부탄올 18wt%EC 12wt%Concentrated silica sol 9wt% IPA 58wt% distilled water 3wt% 1-butanol 18wt% EC 12wt% 농축 실리카졸 8.5wt%IPA 58.5wt%증류수 3wt%1-부탄올 18wt%EC 12wt%Concentrated silica sol 8.5wt% IPA 58.5wt% distilled water 3wt% 1-butanol 18wt% EC 12wt% 점도1)Viscosity1) 2.1cps2.1cps 2.0cps2.0cps 분자량(Mw)Molecular Weight (Mw) 12301230 12201220 pHpH 1.0~3.01.0-3.0 1.0~3.01.0-3.0 표면장력2)Surface tension2) 26dyne/cm26dyne / cm 25.5dyne/cm25.5 dyne / cm

1) 점도: BROOKFIELD VISCOMETER 모델 DV-II를 사용하여 Corn & Plate 방식으로1) Viscosity: Corn & Plate Method using BROOKFIELD VISCOMETER Model DV-II

25℃에서 spindle no. 1, 60rpm 조건에서 측정함Spindle no. Measured at 1, 60 rpm

2) 표면장력: KRUSS사(Germany)를 이용하여 25℃에서 측정함2) Surface tension: measured at 25 ℃ using KRUSS (Germany)

상기에서 농축 실리카졸 및 완성된 2차 코팅액은 저장안정성을 위해 0 내지 -10℃ 에서 냉동보관 하였다.The concentrated silica sol and the completed secondary coating solution was stored frozen at 0 to -10 ℃ for storage stability.

실시예 1~8Examples 1-8

상기 제조예 1~4에서 제조된 각각의 1차 코팅액을 산으로 깨끗이 세척 후 건조된 유리기판 표면위에 스핀 코팅하고 약 80초간 건조시켜 제 1 코팅층을 형성시켰다. 이때 회전속도는 130rpm, 코팅시간은 70초로 하였다. 이와 같이 형성된 제 1 코팅층 위에 상기 제조예 5 또는 6으로부터 수득한 2차 코팅액을 상기 1차 코팅시와 동일한 조건으로 스핀 코팅한 후 건조시켜 제 2 코팅층을 형성시켰다. 이어서, 185℃에서 약 80분 정도 소성하였다.Each primary coating solution prepared in Preparation Examples 1 to 4 was washed with acid, spin coated on the dried glass substrate, and dried for about 80 seconds to form a first coating layer. At this time, the rotation speed was 130rpm, the coating time was 70 seconds. The second coating solution obtained from Preparation Example 5 or 6 on the first coating layer thus formed was spin-coated under the same conditions as in the first coating and then dried to form a second coating layer. Subsequently, baking was carried out at 185 ° C. for about 80 minutes.

이와 같이 형성된 코팅필름의 물성평가는 전도도의 경우 미츠비시 케미칼(MITSUBISHI CHEMICAL)사의 Loresta(4-point probe)를 사용하여 단위 면적당 표면저항으로 평가하였고, 투과도는 UV-가시광선 스펙트로미터를 사용하여 550nm에서의 투과도로 평가하였으며, 반사율은 PSI사의 반사율 계측기(DARSA PRO-5000)를 사용하여 측정하였고, 막경도는 연필경도계를 이용하여 측정하였다. 평가결과는 하기 표 3과 같다.The physical properties of the coating film formed as described above were evaluated by surface resistance per unit area using Loresta (4-point probe) manufactured by Mitsubishi Chemical in the case of conductivity, and the transmittance was measured at 550 nm using a UV-visible spectrometer. The transmittance was measured by using a reflectance measuring device (DARSA PRO-5000) of PSI, and the film hardness was measured using a pencil hardness tester. Evaluation results are shown in Table 3 below.

구분division 코팅액의 종류Type of coating solution 코팅막의 물성Properties of Coating Film 1차 코팅액Primary coating solution 2차 코팅액Secondary coating solution 표면저항(Ω/□ )Surface resistance (Ω / □) 투과도(T%)Permeability (T%) 반사율(%)reflectivity(%) 막경도Film hardness 외관Exterior 실시예 1Example 1 제조예 1Preparation Example 1 제조예 5Preparation Example 5 6.0E026.0E02 6666 0.140.14 8H8H BluishBlurish 실시예 2Example 2 제조예 2Preparation Example 2 제조예 5Preparation Example 5 8.0E028.0E02 6565 0.150.15 8H8H BluishBlurish 실시예 3Example 3 제조예 3Preparation Example 3 제조예 5Preparation Example 5 8.5E028.5E02 6565 0.200.20 8H8H BluishBlurish 실시예 4Example 4 제조예 4Preparation Example 4 제조예 5Preparation Example 5 1.0E031.0E03 6565 0.210.21 8H8H BluishBlurish 실시예 5Example 5 제조예 1Preparation Example 1 제조예 6Preparation Example 6 2.5E032.5E03 6565 0.250.25 7H7H BluishBlurish 실시예 6Example 6 제조예 2Preparation Example 2 제조예 6Preparation Example 6 3.5E033.5E03 6565 0.240.24 7H7H BluishBlurish 실시예 7Example 7 제조예 3Preparation Example 3 제조예 6Preparation Example 6 5.0E035.0E03 6464 0.200.20 7H7H BluishBlurish 실시예 8Example 8 제조예 4Preparation Example 4 제조예 6Preparation Example 6 6.0E036.0E03 6565 0.240.24 7H7H BluishBlurish

이상에서 상세히 설명한 바와 같이, 본 발명의 코팅액 조성물은 도전성이 우수함과 동시에 저투과, 저반사 특성을 가지므로, 특히 평판디스플레이(flat display)용 CRT(cathode ray tube)의 외면 유리 코팅에 유용하다.As described in detail above, the coating liquid composition of the present invention is excellent in conductivity, and has low permeability and low reflection properties, and thus is particularly useful for outer glass coating of a cathode ray tube (CRT) for a flat display.

Claims (12)

다음을 포함하는 전자파 차폐용 도전성 블랙착색 코팅액 조성물:Conductive black coloring coating liquid composition for electromagnetic shielding comprising: (a) Ag-Au 졸;(a) Ag-Au sol; (b) 폴리스티렌술포네이트(PSS)로 도프된 폴리에틸렌디옥시티오펜(PEDT);(b) polyethylenedioxythiophene (PEDT) doped with polystyrenesulfonate (PSS); (c) 알콕시실란;(c) alkoxysilanes; (d) 카본블랙;(d) carbon black; (e) 무기안료; 및(e) inorganic pigments; And (f) 탄소수 1~7개의 알코올 용매.(f) Alcohol solvents having 1 to 7 carbon atoms. 제 1항에 있어서,The method of claim 1, (a) Ag-Au 졸(고형분 함량 0.8~1.4중량%) 10~30중량%;(a) 10-30% by weight of Ag-Au sol (solid content 0.8-1.4% by weight); (b) 폴리스티렌술포네이트(PSS)로 도프된 폴리에틸렌디옥시티오펜(PEDT) 수용액(고형분 함량 1.2~1.5중량%) 0.1~5중량%;(b) 0.1 to 5% by weight aqueous polyethylenedioxythiophene (PEDT) (solid content 1.2 to 1.5% by weight) doped with polystyrenesulfonate (PSS); (c) 알콕시실란 0.1~0.3중량%;(c) 0.1 to 0.3% by weight of alkoxysilane; (d) 카본블랙 분산액(고형분 함량 2~4중량%)과 (e)무기안료(고형분 함량 2~4중량%)의 혼합물 5~8중량%; 및(d) 5-8% by weight of a mixture of carbon black dispersion (2-4 wt% solids) and (e) inorganic pigment (2-4 wt% solids); And (f) 탄소수 1~7개의 알코올 용매 60~85중량%를 포함하는 것을 특징으로 하는 전자파 차폐용 도전성 블랙착색 코팅액 조성물.(f) A conductive black coloring coating liquid composition for electromagnetic shielding, comprising 60 to 85% by weight of an alcohol solvent having 1 to 7 carbon atoms. 제 1항 또는 제 2항에 있어서, 상기 Ag-Au 졸이 Au로 코팅된 입경 10~50nm의 Ag 미립자를 포함하는 것을 특징으로 하는 전자파 차폐용 도전성 블랙착색 코팅액 조성물.The conductive black coating composition for electromagnetic wave shielding according to claim 1 or 2, wherein the Ag-Au sol comprises Ag fine particles having a particle size of 10 to 50 nm coated with Au. 제 1항 또는 제 2항에 있어서, 상기 알콕시실란이 테트라에톡시실란(TEOS) 또는 테트라메톡시실란(TMOS)인 것을 특징으로 하는 전자파 차폐용 도전성 블랙착색 코팅액 조성물.The conductive black coloring coating liquid composition for electromagnetic wave shielding according to claim 1 or 2, wherein the alkoxysilane is tetraethoxysilane (TEOS) or tetramethoxysilane (TMOS). 제 1항 또는 제 2항에 있어서, 상기 무기안료가 질화티타늄(TiN), 코발트(Co) 및 주석(Sn)으로 구성된 군에서 선택되는 1종 이상인 것을 특징으로 하는 전자파 차폐용 도전성 블랙착색 코팅액 조성물.The conductive black coloring coating liquid composition according to claim 1 or 2, wherein the inorganic pigment is at least one selected from the group consisting of titanium nitride (TiN), cobalt (Co) and tin (Sn). . 제 1항 또는 제 2항에 있어서, 상기 알코올 용매가 이소프로필 알코올(IPA), 에틸셀로솔브(EC), 에탄올(EtOH), 프로필렌 글리콜 모노메틸 에테르(PGM) 및 디아세톤 알코올(DAA)로 구성된 군에서 선택되는 1종 이상인 것을 특징으로 하는 전자파 차폐용 도전성 블랙착색 코팅액 조성물.The method of claim 1 or 2, wherein the alcohol solvent is isopropyl alcohol (IPA), ethyl cellosolve (EC), ethanol (EtOH), propylene glycol monomethyl ether (PGM) and diacetone alcohol (DAA) Electroconductive shielding conductive black coloring coating liquid composition, characterized in that at least one selected from the group consisting of. 다음의 단계들을 포함하는 전자파 차폐용 도전성 블랙착색 코팅필름의 제조방법:Method for producing a conductive black colored coating film for electromagnetic shielding comprising the following steps: (i) 제 1항의 전자파 차폐용 도전성 블랙착색 코팅액 조성물을 세척된 CRT외면 유리 표면에 코팅 후 건조시켜 제 1 코팅층을 형성하는 단계;(i) coating and drying the conductive black colored coating liquid composition for shielding electromagnetic waves on the washed CRT outer glass surface to form a first coating layer; (ii) 상기 제 1 코팅층 위에 2차 코팅액으로서 실리카졸을 코팅하고 건조시켜 제 2 코팅층을 형성하는 단계; 및(ii) coating and drying the silica sol as a secondary coating solution on the first coating layer to form a second coating layer; And (iii) 상기 제 1 및 제 2 코팅층을 열소성하는 단계.(iii) thermally firing the first and second coating layers. 제 7항에 있어서, 상기 실리카졸의 분자량(Mw)이 1200~1500인 것을 특징으로 하는 전자파 차폐용 도전성 블랙착색 코팅필름의 제조방법.The method of manufacturing a conductive black colored coating film for electromagnetic wave shielding according to claim 7, wherein the silica sol has a molecular weight (Mw) of 1200 to 1500. 제 7항에 있어서, 상기 코팅이 스핀 코팅 또는 스프레이 코팅인 것을 특징으로 하는 전자파 차폐용 도전성 블랙착색 코팅필름의 제조방법.The method of manufacturing a conductive black colored coating film for electromagnetic wave shielding according to claim 7, wherein the coating is spin coating or spray coating. 제 9항에 있어서, 상기 스핀 코팅이 회전속도 80~150rpm으로 50~80초 동안 수행되는 것을 특징으로 하는 전자파 차폐용 도전성 블랙착색 코팅필름의 제조방법.10. The method of claim 9, wherein the spin coating is performed at a rotational speed of 80 to 150 rpm for 50 to 80 seconds. 제 7항에 있어서, 상기 열소성이 180~200℃에서 60~90분 동안 수행되는 것을 특징으로 하는 전자파 차폐용 도전성 블랙착색 코팅필름의 제조방법.The method of manufacturing a conductive black colored coating film for electromagnetic wave shielding according to claim 7, wherein the thermal firing is performed at 180 to 200 ° C. for 60 to 90 minutes. 제 7항의 방법에 의해 제조된 표면저항 102내지 103Ω/□, 투과도60%~70%, 경도 6H~9H, 및 반사율 0.5% 이하의 특성을 갖는 전자파 차폐용 도전성 블랙착색 코팅필름.A conductive black colored coating film for electromagnetic wave shielding having the properties of the surface resistance 10 2 to 10 3 Ω / □, transmittance 60% to 70%, hardness 6H to 9H, and reflectance 0.5% or less prepared by the method of claim 7.
KR10-2002-0023621A 2002-04-30 2002-04-30 Electroconductive black-colored coating composition for shielding electromagnetic waves, method for forming coating film using the same and the coating film formed thereby KR100475549B1 (en)

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KR100803256B1 (en) * 2007-06-05 2008-02-13 (주)하우켐 Coating composition for intercepting the light and shielding electric wave at the same time
KR20220096533A (en) * 2020-12-31 2022-07-07 주식회사 솔루에타 High Elasticity and high conductivity black film, and method of fabricating of the same

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DE19633311A1 (en) * 1996-08-19 1998-02-26 Bayer Ag Scratch-resistant conductive coatings
JP3399268B2 (en) * 1996-12-18 2003-04-21 三菱マテリアル株式会社 Transparent black conductive film
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KR100803256B1 (en) * 2007-06-05 2008-02-13 (주)하우켐 Coating composition for intercepting the light and shielding electric wave at the same time
KR20220096533A (en) * 2020-12-31 2022-07-07 주식회사 솔루에타 High Elasticity and high conductivity black film, and method of fabricating of the same

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