KR20020034040A - UV Curable Back Light Ink and Prepartion Thereof - Google Patents

UV Curable Back Light Ink and Prepartion Thereof Download PDF

Info

Publication number
KR20020034040A
KR20020034040A KR1020000064826A KR20000064826A KR20020034040A KR 20020034040 A KR20020034040 A KR 20020034040A KR 1020000064826 A KR1020000064826 A KR 1020000064826A KR 20000064826 A KR20000064826 A KR 20000064826A KR 20020034040 A KR20020034040 A KR 20020034040A
Authority
KR
South Korea
Prior art keywords
ink
backlight
silane
weight
curable
Prior art date
Application number
KR1020000064826A
Other languages
Korean (ko)
Other versions
KR100400238B1 (en
Inventor
이대성
김준범
류재명
Original Assignee
오주언
삼성화학페인트주식회사
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 오주언, 삼성화학페인트주식회사 filed Critical 오주언
Priority to KR10-2000-0064826A priority Critical patent/KR100400238B1/en
Publication of KR20020034040A publication Critical patent/KR20020034040A/en
Application granted granted Critical
Publication of KR100400238B1 publication Critical patent/KR100400238B1/en

Links

Classifications

    • 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
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/10Printing inks based on artificial resins
    • C09D11/101Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
    • 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
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/03Printing inks characterised by features other than the chemical nature of the binder
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nonlinear Science (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

PURPOSE: Provided is an ink for a UV curing type backlight of an LCD, which can prevent the change in quality compared to an ink for a thermosetting backlight and can improve the drying speed of the ink and the brightness of the backlight. CONSTITUTION: The ink for the UV curing type backlight is produced by a process comprising the steps of: mixing tetramethoxy silane and 0.1-1.0% HCl water solution in the weight ratio of 2:1-3:1; adding 20-50wt% of an acryloxy-functional silane to the mixture to obtain a colloidal silica solution of which the surface is treated by the acryloxy-functional silane, wherein the acryloxy-functional silane is at least one selected from the group consisting of acryloxypropyl trimethoxy silane, acryloxypropyl triethoxy silane, methacryloxypropyl methyl diethoxy silane, and etc.; adding 20-50wt% of hexanediol diacrylate to the silica solution; eliminating an alcohol solution and moisture; adding 5-15wt% of epoxy acrylate, 1-5wt% of isobutylbenzene ether, and 5-12wt% of a filler containing SiO2, TiO2, and BaSO4 having an average particle size of less than 10 micrometer.

Description

유브이 경화형 백라이트용 잉크 및 그 제조방법{UV Curable Back Light Ink and Prepartion Thereof}UV curable backlight ink and its manufacturing method {UV Curable Back Light Ink and Prepartion Thereof}

본 발명은 액정표시장치(Liquid Crystal Display :LCD)의 UV경화형 백라이트용 잉크 및 그 제조방법에 관한 것으로, 더욱 상세하게는 acryloxyfunctional silane으로 표면 처리한 콜로이달 실리카 바인더에 산란입자가 분산된 백라이트용 잉크 및 그 제조방법에 관한 것이다.The present invention relates to a UV-curable backlight ink of a liquid crystal display (LCD) and a manufacturing method thereof, and more particularly, to a backlight ink in which scattering particles are dispersed in a colloidal silica binder surface-treated with acryloxyfunctional silane. And to a method for producing the same.

전자 제품의 소형화, 경량화 추세에 들어선 시점에서, 텔레비전을 비롯해서 계측기기, 정보 단말기기 등의 모니터에 주로 사용되는 CRT(Cathode Ray Tube)는 자체의 큰 무게나 크기로 인하여 소형, 경량화 요구에 적극 대응할 수 없었다. 따라서, 이를 대체하기 위해 소형, 경량화의 장점을 갖고 있는 액정표시장치(LCD)의 개발이 활발히 진행되어 왔고, 근래에는 평판 표시장치로서의 역할을 충분히 수행할 수 있을 정도이며, 그 수요가 계속 증가하고 있다.With the trend toward miniaturization and lightening of electronic products, the CRT (Cathode Ray Tube), which is mainly used for monitors such as televisions, measuring devices, and information terminal devices, is able to respond to the demands for small size and light weight due to its large weight and size. Could not. Therefore, the development of liquid crystal display (LCD), which has the advantages of small size and light weight, has been actively progressed in order to replace it, and in recent years, it is enough to play a role as a flat panel display device, and the demand is continuously increasing. have.

그러나, 액정표시장치(LCD)는 자체 발광을 하지 못하고, 투과광의 양을 변조(modulation)시키는 역할만 하므로, 액정을 사용한 모니터 화면을 균일하게 조사하는 백라이트 어셈블리가 LCD패널의 후방에 설치되어져야한다. 이 면광원 형태의 백라이트에 요구되는 성능은 표시면 전체의 휘도가 균일해야 하며, 액정 패널의 투과율이 10% 미만인 것을 고려하여 충분한 휘도가 유지되어야한다.However, since the liquid crystal display (LCD) does not emit light by itself and only modulates the amount of transmitted light, a backlight assembly for uniformly irradiating a monitor screen using liquid crystal should be installed at the rear of the LCD panel. . The performance required for the backlight in the form of surface light source should be uniform in the luminance of the entire display surface, and sufficient luminance should be maintained in consideration that the transmittance of the liquid crystal panel is less than 10%.

도 1에 나타낸 것과 같이, 종래의 램프 어셈블리는 LCD패널의 전면으로 광을 전달하도록 LCD패널의 후면에 백라이트 어셈블리(Backlight Assembly)가 설치된다. 백라이트 어셈블리는 LCD패널의 후면 모서리에 발광램프(5)와 램프 반사판(4)으로 구성된 램프 어셈블리가 설치되고, 발광램프(5)로부터의 광선과 램프 반사판(4)으로부터의 광선을 LCD패널(1)의 전면으로 균일하게 유도하도록 도광판(6)이 설치되며, 도광판(6)의 후면에 반사판(8)이 부착되고, 도광판(6)으로부터 유도된 광선을 확산하고 집광하는 확산판(3)과 프리즘(2)과 같은 시트류가 도광판(6)과 LCD패널(1) 사이에 설치되도록 구성되어있다. 도광판(6) 하단부는 잉크가 도트 형태를 한 패턴으로 인쇄되고 램프에서 가까운 부분은 작게, 먼 부분은 더 큰 크기의 도트로 형성되어 반사량을 조절하며 백라이트 면 전체에 균일한 휘도 분포를 갖게 만든다.As shown in FIG. 1, the conventional lamp assembly includes a backlight assembly installed at the rear of the LCD panel to transmit light to the front of the LCD panel. The backlight assembly is provided with a lamp assembly composed of a light emitting lamp 5 and a lamp reflector 4 at the rear edge of the LCD panel, and the light beam from the light emitting lamp 5 and the light beam from the lamp reflector 4 are disposed on the LCD panel 1. A light guide plate 6 is installed to uniformly guide the front of the light guide plate, and a reflecting plate 8 is attached to a rear surface of the light guide plate 6, and a diffuser plate 3 for diffusing and condensing the light guided from the light guide plate 6; Sheets such as the prism 2 are configured to be installed between the light guide plate 6 and the LCD panel 1. The lower part of the light guide plate 6 is printed in a pattern in which the ink is dot-shaped, and the portion near the lamp is made small and the far portion is formed of dots of larger size to control the amount of reflection and to have a uniform luminance distribution over the entire backlight surface.

이와 같이 구성되는 종래의 백라이트 어셈블리는 제품의 기술 경쟁력 우위를 판단하는 척도인 고휘도화와 박형화를 위해 고휘도 시트, 고휘도 발광램프, 고휘도 기구 구조 등의 개발에 집중되어 왔다.The conventional backlight assembly configured as described above has been concentrated on the development of high brightness sheets, high brightness light emitting lamps, high brightness mechanism structures, etc., for high brightness and thinness, which are a measure for determining the technological competitiveness of a product.

그 중에서 도광판(6) 하단부에 인쇄되는 잉크는 열경화형으로 많은 연구가 되어왔다. 그러나 열경화시 발생하는 열에 의해 재질이 변질 될 가능성과 건조 속도가 늦다는 단점이 있다. 따라서, 이와 같은 단점을 극복하기 위해서는 건조 속도가 빠르며, 또한 열에 의한 재질의 변질 가능성이 없는 백라이트용 잉크가 요구 되어지고 있다.Among them, the ink printed on the lower part of the light guide plate 6 has been studied in a thermosetting type. However, there is a disadvantage that the material is deteriorated by the heat generated during thermal curing and the drying speed is low. Therefore, in order to overcome such drawbacks, there is a need for a backlight ink which has a high drying speed and no possibility of material deterioration due to heat.

본 발명은 상기한 바와 같은 제반 문제를 해결하기 위한 것으로, 백라이트용잉크의 제조시 잉크의 건조 속도를 빠르게 하여 작업 능률을 올리고, UV경화법을 사용하여 열경화로 인한 재질의 변질을 방지하는 UV 경화형 백라이트용 잉크의 제조방법을 제공하는 것을 목적으로 한다.The present invention is to solve the above-mentioned problems, to improve the work efficiency by increasing the drying speed of the ink during the manufacture of the backlight ink, UV to prevent the deterioration of the material due to thermal curing by using the UV curing method It is an object to provide a method for producing a curable backlight ink.

또한, 본 발명의 다른 목적은 종래의 백라이트용 잉크보다 산란 효과와 광투과성이 좋은 콜로이달 실리카를 사용하여 균일한 산란 입자의 배열로 LCD의 균일한 면광원을 유지하고 휘도를 증가시키는 UV 경화형 백라이트용 잉크를 제공하는 것이다.In addition, another object of the present invention is to use a colloidal silica with better scattering effect and light transmittance than the conventional backlight ink, UV-curable backlight to maintain a uniform surface light source of the LCD by increasing the brightness of the uniform scattering particles It is to provide ink for.

도 1은 종래기술의 LCD 백라이트 어셈블리의 개략도이다.1 is a schematic diagram of a prior art LCD backlight assembly.

도 2는 종래기술의 UV경화기구 개념도이다.2 is a conceptual view of the UV curing mechanism of the prior art.

도 3은 본 발명에 의한 UV경화형 백라이트 잉크층의 개략도이다.3 is a schematic diagram of a UV-curable backlight ink layer according to the present invention.

도 4는 LCD 패널의 휘도 측정 포인트에 대한 개략도이다4 is a schematic diagram of luminance measurement points of an LCD panel;

<도면의 주요부분에 대한 부호의 설명><Description of the symbols for the main parts of the drawings>

1 : LCD 패널 2 : 프리즘 3 : 확산판1 LCD Panel 2 Prism 3 Diffusion Plate

4 : 램프 반사판 5 : 발광램프 6 : 도광판4 lamp reflector 5 light emitting lamp 6 light guide plate

7 : 도트 인쇄층 8 : 반사판 9 : 콜로이달 실리카7 dot printed layer 8 reflector 9 colloidal silica

10 : 충전재10: filling material

본 발명의 UV경화형 백라이트용 잉크의 제조방법은 silane과 산성용액을 2:1 내지 3:1로 혼합하여 시간과 온도를 조절하여 반응한 후, 원하는 입자크기의 콜로이달 실리카 용액을 얻은 다음, 콜로이달 실리카를 acryloxyfunctional silane으로 표면처리하여 아크릴 관능기를 갖는 콜로이달 실리카를 얻은 후 광개시제와 충전재(filler)를 첨가하는 것이다.In the method of preparing the UV-curable backlight ink of the present invention, after mixing the silane and the acid solution at 2: 1 to 3: 1 and reacting by controlling the time and temperature, a colloidal silica solution having a desired particle size is obtained, and then This month, the surface of the silica is acryloxyfunctional silane to obtain a colloidal silica having an acrylic functional group, and then a photoinitiator and a filler are added.

본 발명의 백라이트 발생방법은 상기와 같이 제조된 UV경화형 백라이트용 잉크를 액정표시장치(LCD) 모듈의 백라이트 어셈블리의 도광판 하단면에 도트 인쇄하여, 도광판 내부로 유도된 광을 효율적으로 산란시켜 균일한 면광원이 전면으로 나아가게 한 것이다.In the backlight generation method of the present invention, the UV-curable backlight ink prepared as described above is dot-printed on the bottom surface of the light guide plate of the backlight assembly of the LCD module, thereby efficiently scattering the light guided into the light guide plate and The surface light source is brought to the front.

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

본 발명의 제조방법은, 먼저, silane이 든 용기를 40 ~ 60℃로 유지하며 0.1 내지 1.0% HCl 수용액을 서서히 적가한다. 이 때 silane과 HCl 수용액의 비율이 2:1 내지 3:1이 되도록 혼합하여 2 ~ 3시간 동안 반응시킨다. silane의 비율이 상기범위 이상일 경우에는 콜로이달 실리카가 형성되지 않고, 상기범위 미만일 경우에는 콜로이달 실리카의 입자 크기가 너무 커지는 문제점이 있다. 혼합될 수 있는 silane으로는 4관능기를 갖는 tetramethoxysilane과 tetraethoxysilane 또는 3관능기를 갖는 methyltrimethoxysilane 등이 있다. 또한 HCl 수용액의 농도가 상기범위 이상일 경우에는 혼합된 용액이 쉽게 겔화되고, 상기범위 미만일 경우에는 콜로이달 실리카가 형성되지 않는 문제점이 있다.In the production method of the present invention, first, the vessel containing silane is slowly added dropwise to 0.1-1.0% HCl aqueous solution while maintaining the temperature at 40-60 ° C. At this time, the mixture of silane and HCl aqueous solution is 2: 1 to 3: 1 and mixed for 2 to 3 hours. If the ratio of silane is greater than or equal to the above range, no colloidal silica is formed, and if it is less than the range, the particle size of the colloidal silica is too large. Silanes that can be mixed include tetramethoxysilane and tetraethoxysilane with tetrafunctional groups or methyltrimethoxysilane with trifunctional groups. In addition, when the concentration of the HCl aqueous solution is more than the above range, the mixed solution is easily gelled, if less than the above range there is a problem that the colloidal silica is not formed.

이어서, 콜로이달 입자 크기가 대략 20 ~ 100㎚로 형성된 상기 용액에 acryloxyfunctional silane을 20 내지 50 무게% 첨가하여 40 ~ 60℃에서 2 ~ 3시간 동안 반응시켜 표면이 acryloxyfunctional silane으로 처리된 콜로이달 실리카를 얻는다. acryloxyfunctional silane의 첨가비율이 상기범위 이상일 경우에는 인쇄된 잉크의 도막에 연성이 부여되지 않아 갈라짐 현상이 생기고, 상기범위 미만일 경우에는 도막의 부착성이 떨어지는 문제점이 있다. 첨가된 acryloxyfunctional silane으로는 acryloxypropyltrimethoxysilane, acryloxypropyltriethoxysilane, acryloxymethyldimethylacryloxysilane, N-(3-acryloxy-2-hydroxypropyl)- 3-aminopropyltriethoxysilane, acryloxypropyldimethylmethoxysilane, acryloxypropylmethyldimethoxysilane, methacryloxymethylphenyldimethylsilane, methacryloxyethoxytrimethylsilane, methacrylamidopropyltrimethoxysilane, methacryloxymethyltriethoxysilane, methacryloxyemthyltrimethoxysilane, methacryloxypropylmethyldiethoxysilane 중에서 선택된 적어도 1종 이상을 포함한다.Subsequently, 20 to 50% by weight of acryloxyfunctional silane was added to the solution having a colloidal particle size of about 20 to 100 nm and reacted at 40 to 60 ° C. for 2 to 3 hours to obtain a colloidal silica surface treated with acryloxyfunctional silane. Get When the addition ratio of acryloxyfunctional silane is more than the above range, ductility is not given to the coating film of the printed ink, so that a cracking phenomenon occurs, and when it is less than the above range, the adhesion of the coating film is inferior. Among the added acryloxyfunctional silanes, acryloxypropyltrimethoxysilane, acryloxypropyltriethoxysilane, acryloxymethyldimethylacryloxysilane, N- (3-acryloxy-2-hydroxypropyl)-3-aminopropyltriethoxysilane, acryloxypropylmethyldimethoxysilane, methacryloxymethylphenyl methoxy oxy dimethyl aryl, methyl methoxy dimethyl dimethyl methyl methoxy dimethyl methyl methoxy Include.

상기 용액에 acryl monomer를 20 내지 50무게% 첨가한 후, 알코올 용매와 수분을 제거하기 위해 40 ~ 50℃에서 회전증발(rotary evaporation)시킨다. acryl monomer의 첨가비율이 상기범위 이상일 경우에는 인쇄 후 도막의 물성이 떨어지고, 상기범위 미만일 경우에는 용매와 수분을 제거할 때 점도가 증가하게 된다. 여기에 사용되어질 수 있는 acryl monomer로는 hexanediol dicarylate, tripropyleneglycol diacrylate, polyethyleneglycol diacrylate, ethoxylated trimethylolpropane triacrylate, methyl methacrylate, 2-ethylhexyl acrylate, lauryl methacrylate, 2-hydroxyehtyl methacrylate, hydroxyethyl acrylate, glycidyl methacrylate, n-butyl acrylate, 2-ethylhexyl methacrylate 등이 있다.After adding 20 to 50% by weight of acryl monomer to the solution, rotary evaporation is carried out at 40 ~ 50 ℃ to remove the alcohol solvent and water. If the addition ratio of the acryl monomer is above the above range, the physical properties of the coating film after printing is lowered, and below the above range, the viscosity increases when the solvent and water are removed. Acryl monomers that can be used here are hexanediol dicarylate, tripropyleneglycol diacrylate, polyethyleneglycol diacrylate, ethoxylated trimethylolpropane triacrylate, methyl methacrylate, 2-ethylhexyl acrylate, lauryl methacrylate, 2-hydroxyehtyl methacrylate, hydroxyethyl acrylate, glycidyl methacrylate, n-butyl acrylate, ethylhexyl methacrylate.

위와 같은 방법으로 얻은 콜로이달 실리카 용액에 oligomer 5 내지 15무게%, 광개시제 1 내지 5무게%, 그리고 충전재 5 내지 12무게%를 첨가한 후 40℃ 이하에서 30분 동안 교반하게 되면 UV경화형 백라이트용 잉크가 얻어 진다. 여기에서 oligomer 첨가비율이 상기범위 이상일 경우에는 점도가 증가하여 스크린 인쇄 작업성이 떨어지고, 상기범위 미만일 경우에는 도막의 부착성이 떨어지는 문제점이 있다. 그리고 광개시제의 첨가비율이 상기범위 이상일 경우에는 광개시제에 의한 라디칼 반응이 계속 진행되어 경화된 도막을 분해하여 내구성을 떨어뜨리게 되고, 상기범위 미만일 경우에는 경화 속도가 느려지는 문제점이 있다. 또한 충전재의 첨가비율이 상기범위 이상일 경우에는 점도증가로 인해 인쇄 작업성이 떨어지며, 상기범위 미만일 경우에는 산란효율이 떨어진다.UV-curable backlight ink when 5 to 15% by weight of oligomer, 1 to 5% by weight of photoinitiator, and 5 to 12% by weight of filler were added to the colloidal silica solution obtained by the above method and then stirred at 40 ° C. or less for 30 minutes. Is obtained. If the oligomer addition ratio is greater than or equal to the above range, the viscosity is increased and screen printing workability is lowered. When the addition ratio of the photoinitiator is more than the above range, radical reaction by the photoinitiator continues to decompose the cured coating film, thereby lowering the durability, and when the photoinitiator is less than the above range, the curing rate is lowered. In addition, when the addition ratio of the filler is above the above range, the printability is inferior due to the increase in viscosity, and when it is below the above range, the scattering efficiency is lowered.

사용가능한 oligomer로는 urethane acrylate, epoxy acrylate, epoxy methacrylate, melamine acrylate 등이 있다. 광개시제로는 2-hydroxycyclohexylphenyl ketone, 2-hydroxy-2-methyl-1-phenyl propanone, isobutylbenzoin ether, 그리고 2,2-dimethyoxy-2-phenyl acetophenone 등이 있다. 충전재로는 SiO2, Al2O3, ZrO2, TiO2, 그리고 BaSO4등이 있다.Usable oligomers include urethane acrylate, epoxy acrylate, epoxy methacrylate and melamine acrylate. Photoinitiators include 2-hydroxycyclohexylphenyl ketone, 2-hydroxy-2-methyl-1-phenyl propanone, isobutylbenzoin ether, and 2,2-dimethyoxy-2-phenyl acetophenone. Fillers include SiO 2 , Al 2 O 3 , ZrO 2 , TiO 2 , and BaSO 4 .

첨가되는 충전재(filler)는 10㎛ 미만의 평균입자크기를 가진 것을 사용하는 것이 바람직하다. 충전재(filler)의 첨가에 의하여 도광판 내부로 도광된 광을 산란하여 난반사시키는 효과를 얻을 수 있다.The filler to be added is preferably used having an average particle size of less than 10㎛. By adding a filler, scattering of light guided into the light guide plate may be achieved.

본 발명의 실시예는 아래와 같다.An embodiment of the present invention is as follows.

<제조실시예><Production Example>

먼저, tetramethoxysilane이 든 용기를 50℃로 유지하며 0.5% HCl 수용액을 서서히 적가한다. 이 때 tetramethoxysilane과 HCl 수용액의 비율이 2:1 내지 3:1이 되도록 혼합하며 3시간 동안 반응하였다. 이어서, acryloxypropyltrimethoxysilane을 40 무게% 첨가하여 50℃에서 3시간 동안 반응시켜 표면이 acryloxypropyltrimethoxysilane으로 처리된 콜로이달 실리카를 얻었다. 얻어진 용액에 hexanediol diacrylate를 40무게% 첨가한 후, 알코올 용매와 수분을 제거하기 위해 45℃에서 회전증발(rotary evaporation)하였다.First, the vessel containing tetramethoxysilane is kept at 50 ° C. and 0.5% HCl aqueous solution is slowly added dropwise. At this time, the mixture of tetramethoxysilane and HCl aqueous solution was 2: 1 to 3: 1 and reacted for 3 hours. Subsequently, 40 wt% of acryloxypropyltrimethoxysilane was added and reacted at 50 ° C. for 3 hours to obtain colloidal silica whose surface was treated with acryloxypropyltrimethoxysilane. 40% by weight of hexanediol diacrylate was added to the resulting solution, followed by rotary evaporation at 45 ° C. to remove alcohol solvent and water.

상기의 방법으로 얻은 콜로이달 실리카 용액에 10무게%의 epoxy acrylate, 3무게%의 isobutylbenzoin ether , 그리고 평균입경 7㎛ 의 SiO2, TiO2, 그리고 BaSO4가 동일 비율로 혼합된 충전재(filler)를 투입한 후 40℃ 이하에서 Dispermat(독일, VMA-Getzmann 사)으로 30분 정도 분산하여 UV경화형 백라이트용 잉크를 제조하였다.In the colloidal silica solution obtained by the above method, a filler containing 10% by weight of epoxy acrylate, 3% by weight of isobutylbenzoin ether, and SiO 2 , TiO 2 , and BaSO 4 with an average particle diameter of 7 μm was mixed in the same ratio. After the addition, it was dispersed for about 30 minutes with Dispermat (Germany, VMA-Getzmann) at 40 ° C. or less to prepare a UV-curable backlight ink.

<비교제조예><Comparative Manufacturing Example>

본 발명자의 선행기술인 대한민국 특허출원 제 2000-58772호에 의거하여, 톨루엔, 크실렌 및 시크로헥사논(cyclohexanone)이 동일 비율 조성으로 혼합된 혼합용매에 30무게%의 분자량 100,000의 acrylic copolymer와 분자량 30,000의 vinyl copolymer를 용해시켰다. 이 용액을 ethylene oxide기와 propylene oxide기를 함유한 분자량 25,000의 polydimethylsiloxane과 혼합한 후, 130℃의 온도에서 300rpm의 속도로 2시간 동안 교반한 후, 온도를 60℃ 이하로 낮추고 tetraethoxysilane과 methyl tetramethoxysilane이 8무게% 함유된 메탄올용액을 2시간 동안 적가하였다. 동일 조건에서 1시간 동안 유지시킨 후 aminomethylpropanol과 메탄올이 1:1 무게비로 혼합된 용액을 30분 동안 적가하고 같은 조건으로 4시간 동안 유지시킨 다음, 평균입경 7㎛ 의 SiO2, TiO2, 그리고 BaSO4를 동일 비율로 혼합된 충전재를 투입한 후 Dispermat(독일, VMA-Getzmann 사)로 30분 정도 분산하여 열경화형 백라이트용 잉크를 제조하였다.According to the prior art of the Republic of Korea Patent Application No. 2000-58772 of the present inventors, an acrylic copolymer having a molecular weight of 30% by weight and a molecular weight of 30,000 in a mixed solvent in which toluene, xylene and cyclohexanone are mixed in the same ratio composition Vinyl copolymer was dissolved. The solution was mixed with polydimethylsiloxane having a molecular weight of 25,000 containing ethylene oxide and propylene oxide, and then stirred for 2 hours at a speed of 300 rpm at a temperature of 130 ° C., and then the temperature was lowered to 60 ° C. or less, and tetraethoxysilane and methyl tetramethoxysilane were 8 weights. Methanol solution containing% was added dropwise for 2 hours. After maintaining for 1 hour under the same conditions, a solution of aminomethylpropanol and methanol in a 1: 1 weight ratio was added dropwise for 30 minutes, and maintained for 4 hours under the same conditions. Then, SiO 2 , TiO 2 , and BaSO having an average particle diameter of 7 μm were added. 4 was added at the same ratio, and then mixed with Dispermat (VMA-Getzmann, Germany) for about 30 minutes to prepare a thermosetting backlight ink.

<실시예 및 비교예><Examples and Comparative Examples>

제조실시예에 의하여 얻어진 UV경화형 백라이트용 잉크를 액정표시장치(LCD)모듈의 백라이트 어셈블리의 도광판 하단면에 도트 인쇄하여 Fusion Systems사의 Fusion Lamp를 이용하여 UV경화하였다. 이때 경화조건은 line speed가 7.7m/min이었고, 광량은 128.8mJ/cm2이었다. 비교제조예에 의하여 얻어진 열경화형 백라이트용 잉크 또한 위와 같은 방법으로 인쇄하여 60℃ 오븐에서 10분간 건조하였다.UV-curable backlight ink obtained according to the manufacturing example was dot-printed on the bottom surface of the light guide plate of the backlight assembly of the liquid crystal display (LCD) module and UV-cured using Fusion Lamp of Fusion Systems. At this time, the curing conditions were line speed of 7.7m / min, light quantity was 128.8mJ / cm 2 . The thermosetting backlight ink obtained by the Comparative Production Example was also printed in the same manner as above and dried in an oven at 60 ° C. for 10 minutes.

LCD판넬상에서 휘도를 측정한 포인트와 결과를 표 1에 나타내었다. 표1에서 나타난 바와 같이 열경화형보다 UV경화형으로 인쇄한 것이 약 5%( 50 ~ 100 cd/m2) 정도의 휘도 증가율을 보이며 균일도가 향상된다는 것을 알 수 있다.Table 1 shows the points and the results of measuring the luminance on the LCD panel. As shown in Table 1, the printing by UV curing type than the thermosetting type shows about 5% (50-100 cd / m 2 ) of luminance increase and the uniformity is improved.

pointpoint 비교예(단위 cd/m2)Comparative Example (Unit cd / m 2 ) 실시예(단위 cd/m2)Example (Unit cd / m 2 ) 1One 19351935 19951995 22 19191919 20112011 33 19141914 19961996 44 19581958 20172017 55 19191919 19921992 66 17801780 19241924 77 17271727 18481848 88 18361836 18921892 99 18881888 19151915 1010 18921892 19521952 1111 18321832 19451945 1212 17481748 18931893 1313 18111811 19211921 평균값medium 5 points5 points 19291929 20022002 13 points13 points 18581858 19461946 균일도Uniformity 5 points5 points 1.021.02 1.011.01 13 points13 points 12.4312.43 8.778.77

이상의 실시예 및 비교예를 통하여 알 수 있는 바와 같이, 본 발명에 따른 UV경화형 백라이트용 잉크는 열경화형 백라이트용 잉크와 비교하여 재질의 변질을 방지할 뿐만 아니라, 잉크의 건조속도 및 백라이트의 휘도를 향상시키는 효과를 발휘한다.As can be seen through the above examples and comparative examples, the UV-curable backlight ink according to the present invention not only prevents the deterioration of materials as compared with the thermosetting backlight ink, but also improves the drying speed of the ink and the brightness of the backlight. It is effective to improve.

Claims (5)

Tetramethoxysilane과 0.1 내지 1.0% HCl 수용액의 무게비율이 2:1 내지 3:1이 되도록 혼합하고, 이 혼합물에 acryloxyfunctional silane을 20 내지 50 무게% 첨가하여 표면이 acryloxyfunctional silane으로 처리된 콜로이달 실리카용액을 얻은 후, 이 실리카용액에 hexanediol diacrylate를 20 내지 50무게% 첨가한 후, 알코올 용매와 수분을 제거하고 epoxy acrylate 5 내지 15무게%, isobutylbenzoin ether 1 내지 5무게%, 그리고 충전재(filler)를 5 내지 12 무게% 첨가하는 단계를 포함하는 것을 특징으로 하는 UV 경화형 백라이트용 잉크의 제조방법.Tetramethoxysilane and 0.1 to 1.0% HCl aqueous solution were mixed so that the weight ratio was 2: 1 to 3: 1, and 20 to 50% by weight of acryloxyfunctional silane was added to the mixture to obtain a colloidal silica solution treated with acryloxyfunctional silane. After the addition of 20 to 50% by weight of hexanediol diacrylate to the silica solution, the alcohol solvent and water were removed, 5 to 15% by weight of epoxy acrylate, 1 to 5% by weight of isobutylbenzoin ether, and 5 to 12 fillers. Method for producing a UV curable backlight ink comprising the step of adding a weight%. 제 1항에 있어서, 첨가하는 acryloxyfunctional silane은 acryloxypropylThe acryloxyfunctional silane to be added is acryloxypropyl. trimethoxysilane, acryloxypropyltriethoxysilane, acryloxymethyldimethyltrimethoxysilane, acryloxypropyltriethoxysilane, acryloxymethyldimethyl acryloxysilane, N-(3-acryloxy-2-hydroxypropyl)-3-aminopropyltriethoxysilane, acryloxypropyldimethylmethoxysilane, acryloxypropylmethyldimethoxysilane, methacryloxymethylphenyldimethylsilane, methacryloxyethoxytrimethylsilane, methacrylamidopropyltrimethoxysilane, methacryloxymethyltriethoxysilane, methacryloxyemthyltrimethoxysilane, methacryloxypropylmethyldiethoxysilane 중에서 선택된 적어도 1종 이상을 포함하는 것을 특징으로 하는 UV경화형 백라이트용 잉크의 제조방법.Acryloxysilane, N- (3-acryloxy-2-hydroxypropyl) -3-aminopropyltriethoxysilane, acryloxypropyldimethylmethoxysilane, acryloxypropylmethyldimethoxysilane, methacryloxymethylphenyldimethylsilane, methacryloxyethoxytrimethylsilane, methacrylamidopropyltrimethoxysilane, methacryloxyemthylsilicone or more, selected from a group of more than 1acryloxymethoxyoxymethyl-methoxysilanes that include at least 1 Method for preparing ink 제 1항에 있어서, 충전재(filler)는 10㎛ 미만의 SiO2, TiO2, 그리고 BaSO4를 함유한 것을 특징으로 하는 UV경화형 백라이트용 잉크의 제조방법.The method of claim 1, wherein the filler contains less than 10 μm of SiO 2 , TiO 2 , and BaSO 4 . 제1항 기재의 방법에 의하여 얻어진 UV경화형 백라이트용 잉크.UV-curable backlight ink obtained by the method of claim 1. 제 4항 기재의 UV경화형 백라이트용 잉크를 액정표시장치(LCD) 모듈의 백라이트 어셈블리의 도광판 하단면에 도트 인쇄하여 냉음극관(CCFL)에서 방출되는 가시광을 효과적으로 산란시켜 균일한 면광원을 유지하는 것을 특징으로 하는 고휘도 백라이트의 발생방법.The UV-curable backlight ink of claim 4 is dot-printed on the bottom surface of the light guide plate of the backlight assembly of the LCD module to effectively scatter visible light emitted from the cold cathode tube (CCFL) to maintain a uniform surface light source. A high brightness backlight generating method.
KR10-2000-0064826A 2000-11-02 2000-11-02 UV Curable Back Light Ink and Prepartion Thereof KR100400238B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR10-2000-0064826A KR100400238B1 (en) 2000-11-02 2000-11-02 UV Curable Back Light Ink and Prepartion Thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR10-2000-0064826A KR100400238B1 (en) 2000-11-02 2000-11-02 UV Curable Back Light Ink and Prepartion Thereof

Publications (2)

Publication Number Publication Date
KR20020034040A true KR20020034040A (en) 2002-05-08
KR100400238B1 KR100400238B1 (en) 2003-10-01

Family

ID=19696827

Family Applications (1)

Application Number Title Priority Date Filing Date
KR10-2000-0064826A KR100400238B1 (en) 2000-11-02 2000-11-02 UV Curable Back Light Ink and Prepartion Thereof

Country Status (1)

Country Link
KR (1) KR100400238B1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110205015A (en) * 2019-07-09 2019-09-06 河源轩朗光电科技有限公司 Reflective coating and its preparation method and application

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62256874A (en) * 1986-05-01 1987-11-09 Toshiba Silicone Co Ltd Production of ultraviolet curable composition
JP2664268B2 (en) * 1990-05-11 1997-10-15 東洋インキ製造株式会社 Polymerizable silica dispersion and curable coating composition using the same
JP3197918B2 (en) * 1991-10-02 2001-08-13 三菱レイヨン株式会社 Coating composition and surface modification method of synthetic resin molded article
JP3096862B2 (en) * 1991-12-02 2000-10-10 三菱レイヨン株式会社 Active energy radiation curable coating composition
JPH09183920A (en) * 1995-12-28 1997-07-15 Puresuteeji:Kk Ultraviolet-curing resin composition for formation of light-reflecting portion, light-reflecting portion made of cured coating film of said composition, and backlight unit made by using the same
JP4050370B2 (en) * 1998-01-07 2008-02-20 株式会社Kri Inorganic-containing photosensitive resin composition and inorganic pattern forming method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110205015A (en) * 2019-07-09 2019-09-06 河源轩朗光电科技有限公司 Reflective coating and its preparation method and application

Also Published As

Publication number Publication date
KR100400238B1 (en) 2003-10-01

Similar Documents

Publication Publication Date Title
KR101937665B1 (en) Composition for forming a quantum dot layer, Quantum dot film, Backlight unit, and Liquid crystal display
KR101686713B1 (en) Method for mamufactuing quantum dot-polymer complex, quantum dot-polymer complex, light conversion film, baclight unit and display devive comprising the same
KR101686736B1 (en) Method for manufactuing quantum dot-polymer complex, quantum dot-polymer complex, light conversion film, baclight unit and display devive comprising the same
CN107402416B (en) Quantum diffusion membrane and manufacturing method thereof
US20140153280A1 (en) Optical member, display device having the same and method for fabricating the same
TWI463216B (en) Multi-functional optic sheet
US20140313692A1 (en) Optical member, display device having the same and method of fabricating the same
WO2018117095A1 (en) Wavelength conversion film and backlight unit
JP2009522618A (en) Optical diffuser with frit base film containing inorganic light diffusing pigments of various particle sizes inside
JP5625281B2 (en) Curable resin composition, cured product thereof, and plastic lens
WO2019142719A1 (en) Dimming laminate and resin spacer for dimming laminate
CN112363260A (en) Integrated light conversion glass diffusion plate and preparation method thereof
JPWO2008090929A1 (en) Light diffusing plate, composition liquid for forming light diffusing layer, and method for producing light diffusing plate
WO2018116882A1 (en) Wavelength conversion film and method for producing wavelength conversion film
KR20110062521A (en) Ultraviolet cured organic-inorganic hybrid resin and the resin composition for optical film
JP4453161B2 (en) Photosensitive paste, display and plasma display member
US7309457B2 (en) Chain inorganic oxide fine particle groups
KR100400238B1 (en) UV Curable Back Light Ink and Prepartion Thereof
JP4639530B2 (en) Photosensitive paste and plasma display
JP5245190B2 (en) Liquid curable composition and cured film
CN110873921A (en) Quantum dot mesh point light guide plate and preparation method thereof
CN111752099B (en) Photosensitive resin composition, application thereof, color filter and image display device
JP2011116914A (en) Fluorescent solution, fluorescent film and use thereof
JP2020132745A (en) Light diffusing thermosetting type resin composition and light diffusing plate using the same
JPH08143776A (en) Silicone gel composition

Legal Events

Date Code Title Description
A201 Request for examination
N231 Notification of change of applicant
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
LAPS Lapse due to unpaid annual fee