EP1397393A1 - Compositions de photo-amorceur - Google Patents

Compositions de photo-amorceur

Info

Publication number
EP1397393A1
EP1397393A1 EP02730185A EP02730185A EP1397393A1 EP 1397393 A1 EP1397393 A1 EP 1397393A1 EP 02730185 A EP02730185 A EP 02730185A EP 02730185 A EP02730185 A EP 02730185A EP 1397393 A1 EP1397393 A1 EP 1397393A1
Authority
EP
European Patent Office
Prior art keywords
photo
initiator
formulation
mixture
ketone
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.)
Withdrawn
Application number
EP02730185A
Other languages
German (de)
English (en)
Inventor
Peter Weissman
Rosalyn Waldo
Larisa Kagansky
Udaykumar Ramanbhai Patel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Allnex Belgium NV SA
Original Assignee
UCB SA
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
Priority claimed from EP01110473A external-priority patent/EP1253155A1/fr
Application filed by UCB SA filed Critical UCB SA
Priority to EP02730185A priority Critical patent/EP1397393A1/fr
Publication of EP1397393A1 publication Critical patent/EP1397393A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00—Processes of polymerisation
    • C08F2/46—Polymerisation initiated by wave energy or particle radiation
    • C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
    • C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D11/00—Inks
    • C09D11/02—Printing inks
    • C09D11/10—Printing inks based on artificial resins
    • C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
    • G03F7/029—Inorganic compounds; Onium compounds; Organic compounds having hetero atoms other than oxygen, nitrogen or sulfur
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
    • G03F7/031—Organic compounds not covered by group G03F7/029

Definitions

  • the present invention relates to improved liquid compositions which have use for example as photo-initiators, such as in inks suitable for use with radiation cured polymers.
  • Inks for use in radiation cured polymers require a photo-initiator to aid the start of polymerisation. It is often necessary or desirable to blend different photo-initiators together in a mixture to improve the sensitive of the photo-initiator over a wide range of different wavelengths so the resultant ink can be more readily cured using incident radiation comprising many different wavelengths.
  • liquid photo-initiators and blends thereof are more convenient to use.
  • Prior art photo-initiator blends are prepared by blending at high temperatures in an oven to keep the mixture liquid. However this is difficult to do and can causes the resultant photo-initiator blends to be less stable (i.e. solid precipitates may form when the photo-initiator is left for extended periods). It would be desirable to provide photo-initiator compounds and/or blends with improved stability; which are substantially liquid at ambient temperatures or lower, which can be mixed together more readily that prior art blends; which are easier to use and/or which can be shipped more easily
  • a mixture of three or more photo-initiators said mixture being a liquid at a temperature at or below ambient; the mixture comprising:
  • a first photo-initiator comprising an optionally substituted hydroxyC ⁇ - ⁇ o alkylC ⁇ -i ⁇ aryl ketone which is liquid at ambient temperature;
  • a second photo-initiator comprising an optionally substituted hydroxy(cycloC3- ⁇ oalkyl)C6-i8aryl ketone which is solid at ambient temperature; and c) One or more of the following photo-initiators each of which may be optionally substituted: an alpha aminoacetophenone, a C6-i8aryl(((C ⁇ - ⁇ o alkyl) ⁇ - C6-i8arylcarbonyl)) ⁇ -3 phosphine oxide, a benzophenone; a benzophenone derivative and/or a hydrocarbo (optionally alkyl or aryl) amino benzoate; where, (i) the first photo-initiator (a) and the second photo-initiator (b) are present in the mixture in a weight ratio of from about 0.8 to about 1.2,
  • the first photo-initiator (a) and the second photo-initiator fb) together comprise from about 15 to about 85 percent by weight of the total mixture.
  • ambient temperature denotes a temperature of 20°C.
  • the first photo-initiator (a) comprises hydroxyC ⁇ -6alkylC6-i2aryl ketone, more preferably hydroxyC ⁇ - alkyl phenyl ketone; most preferably
  • the second photo-initiator (b) comprises hydroxy(cycloC3-6alkyl)C6-i2a ⁇ yl ketone; most preferably hydroxy(cycloC3-6alkyl)phenyl ketone; most preferably 1-hydroxycyclohexyl phenyl ketone (such as that available commercially from CIBA as a white solid under the trade name "Irgacure 184").
  • the third photo-initiator (c) comprises C6-i2aryl(((C ⁇ -6alkyl)2-3C6-i2arylcarbonyl)) ⁇ -2 phosphine oxide; more preferably phenyl((C ⁇ - alkyl)3benzoyl)2 phosphine oxide; most preferably phenyl bis(2,4,6-trimethyl benzoyl) phosphine oxide (such as that available commercially from CIBA as a solid under the trade name "Irgacure 819").
  • the third photo-initiator (c) is benzophenone or a benzophenone derivative.
  • benzophenone derivatives are EBECRYL P36 (an acrylated derivative of benzophenone) or EBECRYUL P37, (a solid benzophenone derivative) both available commercially from UCB chemicals.
  • the weight ratio of the first photo-initiator (a) to the second photo-initiator (b) is from about 0.9 to about 1; 1, more preferably is about 1.0.
  • the first photo-initiator (a) and the second photo-initiator (b) together comprise from about 60% to about 75% by weight of the total mixture.
  • the third photo-initiator (c) comprises from about 25% to about 40% by weight of the total mixture.
  • Optional substituent' and/or Optionally substituted' as used herein signifies the one or more of following groups (or substitution by these groups): carboxy, sulpho, formyl, hydroxy, amino, imino, nitrilo, mercapto, cyano, nitro, methyl, methoxy and/or combinations thereof.
  • These optional groups include all chemically possible combinations in the same moiety of a plurality (preferably two) of the aforementioned groups (e.g. amino and sulphonyl if directly attached to each other represent a sulphamoyl radical).
  • Preferred optional substituents comprise: carboxy, sulpho, hydroxy, amino, mercapto, cyano, methyl and/or methoxy.
  • hydrocarbo may also be used herein to replace other terms such as alkyl or aryl herein where the context allows.
  • a hydrocarbo group denotes any univalent or multivalent moiety (optionally attached to one or more other moieties) which consists of one or more hydrogen atoms and one or more carbon atoms and may comprise saturated, unsaturated and /or aromatic moieties.
  • Hydrocarbo groups may comprise one or more of the following groups.
  • Hydrocarbyl groups comprise univalent groups formed by removing a hydrogen atom from a hydrocarbon.
  • Hydrocarbylene groups comprise divalent groups formed by removing two hydrogen atoms from a hydrocarbon the free valencies of which are not engaged in a double bond.
  • Hydrocarbylidene groups comprise divalent groups (represented by formed by removing two hydrogen atoms from the same carbon atom of a hydrocarbon, the free valencies of which are engaged in a double bond. Hydrocarbylidyne groups comprise trivalent groups (represented by "RC ⁇ "), formed by removing three hydrogen atoms from the same carbon atom of a hydrocarbon the free valencies of which are engaged in a triple bond.
  • Hydrocarbo groups may also comprise saturated carbon to carbon single bonds; unsaturated double and/or triple carbon to carbon bonds (e.g. alkenyl, and/or alkynyl groups respectively) and/or aromatic groups (e.g. aryl) and where indicated may be substituted with other functional groups.
  • 'alkyl' or its equivalent e.g. 'alk'
  • any other hydrocarbo group such as those described herein (e.g. comprising double bonds, triple bonds, aromatic moieties (such as respectively alkenyl, alkynyl and/or aryl) and/or combinations thereof (e.g. aralkyl) as well as any multivalent hydrocarbo species linking two or more moieties (such as bivalent hydrocarbylene radicals e.g. alkylene).
  • Any radical group or moiety mentioned herein e.g. as a substituent
  • a group which comprises a chain of three or more atoms, signifies a group in which the chain wholly or in part may be linear, branched and/or form a ring (including spiro and/or fused rings).
  • the total number of certain atoms is specified for certain substituents for example Ci-Nhydrocarbo, signifies a hydrocarbo moiety comprising from 1 to N carbon atoms.
  • substituents for example Ci-Nhydrocarbo, signifies a hydrocarbo moiety comprising from 1 to N carbon atoms.
  • the substituent may replace any H and/or may be located at any available position on the moiety which is chemically suitable or effective.
  • Such utility may be direct where the material has the required properties for the aforementioned uses and/or indirect where the material has use as a synthetic intermediate and/or diagnostic tool in preparing materials of direct utility.
  • suitable also denotes that a functional group is compatible with producing an effective product.
  • the substituents on a repeating unit in any polymers herein may be selected to improve the compatibility of the materials with the polymers and /or resins in which they may be formulated and/or incorporated for the aforementioned uses.
  • the size and length of the substituents may be selected to optimise the physical entanglement or interlocation with the resin or they may or may not comprise other reactive entities capable of chemically reacting and/or cross-linking with such other resins.
  • moieties, species, groups, repeat units, compounds, oligomers, polymers, materials, mixtures, compositions and/or formulations which comprise and/or are used in some or all of the invention as described herein may exist as one or more different forms such as any of those in the following non exhaustive list: stereoisomers (such as enantiomers (e.g. E and/or Z forms), diastereoisomers and/or geometric isomers); tautomers (e.g.
  • .keto and/or enol forms conformers, salts, zwitterions, complexes (such as chelates, clathrates, interstitial compounds, ligand complexes, organometallic complexes, non-stoichiometric complexes, solvates and/or hydrates); isotopically substituted forms, polymeric configurations [such as homo or copolymers, random, graft or block polymers, linear or branched polymers (e.g. star and/or side branched), cross-linked and/or networked polymers, polymers obtainable from di and/or tri-valent repeat units, dendrimers, polymers of different tacticity (e.g.
  • the present invention comprises and/or uses all such forms, which are effective.
  • composition and/or formulation obtained and/or obtainable by any of the processes of the invention as described herein.
  • a further aspect of the invention comprises a method of preparing an ink comprising the steps of mixing a composition and/or formulation of the invention as described herein with a suitable carrier medium and/or grinder.
  • a still other aspect of the present invention provides an ink obtained and/or obtainable by the preceding method.
  • Preferred inks are those suitable for use in lithographic printing for example for graphic art applications.
  • a still further aspect of the invention provides use of a composition and/or formulation of the invention to make an ink, preferably a lithographic ink.
  • Another further aspect of the invention provides use of an ink of the invention (preferably a lithographic ink) to print an article and /or an article so printed.
  • an ink of the invention preferably a lithographic ink
  • 2-Isopropylthioxanthone (CAS no. 5495-84-1) which is a photo-initiator available commercially as a yellow solid under the trade name "Quanticure ITX'Y TMPEOTA which denotes trimethylolpropane ethoxy triacrylate (CAS no. 28961-43-5) also known as poly(oxy-l,2-ethanediyl), alpha. -hydro-omega. -[(l-oxo-2-propenyl)oxy], -ether with 2-ethyl-2-(hydroxymethyl)-l;3-propanediol (3: 1).
  • DPGDA which denotes dipropylene glycol diacrylate (CAS no. 57472-68-1) also known as 2- propenoic acid, oxybis(methyl-2, l-ethanediyl) ester.
  • BDK which denotes a benzil dimethyl ketal of formula , which is a solid photo-initiator suitable for UV-curable unsaturated polyester and acrylate, based coatings and is available commercially from, for example, ChemFirst Fine Chemicals.
  • Benzophenone (CAS no. 119-61-9) is a known photo-initiator available commercially from UCB Chemicals as a white solid under the trade name "Ebecryl BPO".
  • MEHQ which denotes methyl hydroquinone (CAS no. 150-76-5), an inhibitor also known as the monomethyl ether of hydroquinone, available commercially from Aldrich Chemicals.
  • Polyester acrylate oligomer grinding vehicle for flexographic ink which is available commercially from UCB Chemicals under the trade, mark Ebecryl 812.
  • Carbon black pigment available commercially from Columbian Chemicals under the trade name Raven 450.
  • Copper phthalocyanine colorant available commercially from Ciba, under the trade name
  • Examples 1 to 6 were prepared on Day 1 by blending the components together in the amounts given in Table 1, and each example was placed in a refrigerator on Day 2. The examples were then observed for stability i.e. for the presence of solid precipitates. The examples were transferred into a freezer at 11:00 am on day 14 (i.e. between observations 14(a) and 14(b)). The examples were removed from the freezer on day 23 when the experiment was ended. The observations made are given in Tables 2A and 2B for Examples 2 to 6 (Example 1 was not tested) and comparative examples Comp A and B.
  • the liquid Darocur 1173 is well known to be a good solvent previously it has only been possible to solubilize 20% by weight of other photo-initiators therein such as the Irgacure 819 phosphine oxide.
  • the solid Irgacure 184 leads to a mixture with synergistic and unexpected properties as the new mixture is capable of solubilizing 25% or more of other photo-initiators such as the Irgacure 819 (as shown in Tables 2A to 2B).
  • Tables 2A & 2B a check mark indicates no solid precipitates were observed i.e. the blend was stable.
  • Examples B to D Various conventional pigment concentrates (Examples B to D) were prepared as follows and with reference to Table 3. Ebecryl 812 was manually blended with pigment at a 30% level, then was continuously passed through a three-roll mill to make a pigment concentrate having a desired Hegman grind value.
  • the viscosities of the final inks were measured twenty-four hours after preparation using the Haake RSI 50 RheoStress rheometer. These inks were drawn down onto a polypropylene substrate (applied on outside & wiped with isopropyl) using a Cavanagh proofer and UV cured using the fusion unit equipped with one lamp (600 WPI) 75%, 100 RPM at 190.3 mJ/cm 2 . The ink coatings were shiny and were examined for colour, adhesion and other properties. The results indicate that inks containing the photo-initiator blends of the invention perform comparably to the prior art, with few major differences in the physical properties or the performance. The blends of the invention are easier to prepare and use.
  • Example 11 is a photo-initiator blend of the invention comprising Quantacure EPD, Ebecryl BPO, Irgacure 369, Irgacure 184, Quantacure ITX, and Darocur 1173; and
  • Example 12 is a photo-initiator blend of the invention comprising Quantacure EPD, Irgacure 369, Irgacure 184, Quantacure ITX, and Darocur 1173 (i.e. without the Ebecryl EPO).
  • Control formulations were made comprising the photo-initiator blends of Examples 11 or 12 with an acrylated polyester polymer having an average of 5 to 6 acrylate groups per molecule (available commercially from UCB Chemicals under the trade mark Ebecryl 870). These formulations were evaluated for reactivity and lithographic properties
  • Inks in various colors and black were prepared by adding the photo-initiator blends of Examples 11 and 12 in amounts of 10% and 12% by weight of the ink.
  • basic lithographic properties such as tack and water balance were also measured.
  • Tack was measured using a Thwing-Albert Electronic Inkometer for 3 minutes at 1200 rpm and at a temperature of 32°C
  • Inks using 10% of the photo-initiator blend of Example 11 exhibited reactivities comparable to the Comp M. Increasing the photo-initiator level to 12% caused a 71% increase (on average) in reactivity for the black and cyan inks. Inks using the photo-initiator blend of Example 12 exhibited significant reactivity increases with the black and magenta inks compared to Comp M, however the cyan ink exhibited very slow reactivity. An increase in the photo-initiator level (to 12%) caused a significant increase in the cyan ink's reactivity.
  • Ink tacks were similar regardless of photo-initiator. Inks tested with these photo-initiator blends (Ex 11 & 12) did not show adverse effects on fountain solution conductivity (and thus printability) or on water balance or pick-up. Regardless of photo-initiator colored inks tended to retain more water, while black inks tended to retain less. On the basis of reactivity responsiveness, inks made from Example 11 appear to be particularly suitable for lithographic applications.
  • the following Examples 13 to 15 and the data in Table 8 to 10 show with mixtures of Irgacure 184 and Darocur 1173 one obtains particularly stable liquid blends.
  • the standard letdown vehicle consists of TMPEOTA (59.9%), DPGDA (24%), ITX 4 (25%), BDK 4 (25%), EPD 4 (25%), Irg 369 4 (25%), and MEHQ (0.1%).
  • Example 13 demonstrates the synergistic affect on solubility of using both Irgacure 184 together with Darocur 1173 to form a ambient temperature stable system that contains EPD, Irgacure 369 and BPO.
  • the samples of Example 13 were made by weighing the individual ingredients into a glass container, and heating them in an oven at 60 C C. Then samples were mixed by hand until 100 percent of the components were in a liquid state and the mixture was homogeneous. The samples were then allowed to cool to room temperature, and subsequently transferred to a refrigerator set at 11°C.
  • the stability in days was the amount of time that elapsed in the refrigerator before any crystallization or other instability was noted in the mixture.
  • Table 8 clearly demonstrates the superior stability of the mixtures when Irgacure 184 and Darocur 1173 are used together.
  • Table 9
  • Example 14 demonstrates the synergistic affect on solubility of using both Irgacure 184 together with Darocur 1173 to form a ambient temperature stable system that contains EPD, Irgacure 369 and ITX.
  • the samples of Example 14 were made by weighing the individual ingredients into a glass container, and heating them in an oven at 60°C. Then samples were mixed by hand until 100 percent of the components were in a liquid state and the mixture was homogeneous. The samples were then allowed to cool to room temperature, and subsequently transferred to a refrigerator set at 11°C. The stability in days was the amount of time that elapsed in the refrigerator before any crystallization or other instability was noted in the mixture.
  • the data in Table 9 clearly demonstrate the superior stability of the mixtures when Irgacure 184 and Darocur 1173 are used together.
  • Example 15 demonstrates the synergistic affect on solubility of using both Irgacure 184 together with Darocur 1173 to form a ambient temperature stable system that contains EPD, Irgacure 369, ITX and BPO.
  • the samples of Example 15 were made by weighing the individual ingredients into a glass container, and heating them in an oven at 60°C. Then samples were mixed by hand until 100 percent of the components were in a liquid state and the mixture was homogeneous. The samples were then allowed to cool to room temperature, and subsequently transferred to a refrigerator set at 11°C. The stability in days was the amount of time that elapsed in the refrigerator before any crystallization or other instability was noted in the mixture.
  • the data in Table 10 clearly demonstrate the superior stability of the mixtures when Irgacure 184 and Darocur 1173 are used together.
  • the rheology data in Table 11 is for various inks made with formulations analogous to the ink in Example H of Table 6 herein but substituting each of the photo-initiator systems shown in Table 11 for the standard photo-initiator system used in the Comp G of Table 5.
  • the ink made with Example 16 photo-initiator blend exhibits less good rheology, with a moderate shortness index and high yield point.
  • the Darocur 1173 and Irgacure 184 are substituted at different levels and in each case the rheological performance of the ink improved by lowering the yield point, the shortness index, or both.
  • Example 19 where the shortness index is equal to 1 and there is no (zero) yield stress, indicating nearly Newtonian flow conditions which is the ideal rheological profile for an ink to be used in flexography.
  • This combination of photo-initiators also exhibits excellent stability. This improvement in rheology if completely unanticipated as it is commonly accepted that photo-initiators do not affect the rheology of pigmented systems.

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  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Organic Chemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Polymerisation Methods In General (AREA)
  • Paints Or Removers (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

L'invention porte sur des mélanges de photo-amorceurs pour encres durcissant sous l'effet du rayonnement, comportant trois constituants ou plus, et liquides à la température ambiante ou au-dessus. Lesdits mélanges comprennent: (a) un premier photo-amorceur consistant en un hydroxyC1-10 alkylC6-18aryl cétone facultativement substitué, liquide à la température ambiante; (b) un second photo-amorceur consistant en un hydroxy(cycloC3-10alkyl)C6-18aryl cétone facultativement substitué solide à la température ambiante; et (c) un ou plusieurs des photo-amorceurs suivants pouvant tous être facultativement substitués: un alpha aminoacetophénone, un oxyde de C6-18aryl(((C1-10 alkyl)1-4C6-18arylcarbonyl))1-3 phosphine, un benzophénone; un dérivé de benzophénone, et/ou un hydrocarbo (facultativement alkyle ou aryle) amino benzoate; (i) le premier photo-amorceur (a) et le second photo-amorceur (b) étant présents dans le mélange dans un rapport pondéral d'environ 0,8 à environ 1,2, et (ii) le premier photo-amorceur (a) et le second photo-amorceur (b) formant ensemble entre environ 15 et environ 85 % en poids de la totalité du mélange.
EP02730185A 2001-04-27 2002-04-22 Compositions de photo-amorceur Withdrawn EP1397393A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP02730185A EP1397393A1 (fr) 2001-04-27 2002-04-22 Compositions de photo-amorceur

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
EP01110473 2001-04-27
EP01110473A EP1253155A1 (fr) 2001-04-27 2001-04-27 Compositions de photoinitiateurs
EP01117278 2001-07-17
EP01117278 2001-07-17
PCT/EP2002/004403 WO2002088192A1 (fr) 2001-04-27 2002-04-22 Compositions de photo-amorceur
EP02730185A EP1397393A1 (fr) 2001-04-27 2002-04-22 Compositions de photo-amorceur

Publications (1)

Publication Number Publication Date
EP1397393A1 true EP1397393A1 (fr) 2004-03-17

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
EP02730185A Withdrawn EP1397393A1 (fr) 2001-04-27 2002-04-22 Compositions de photo-amorceur

Country Status (7)

Country Link
EP (1) EP1397393A1 (fr)
JP (1) JP2004534117A (fr)
KR (1) KR20040015181A (fr)
CN (1) CN1511166A (fr)
CA (1) CA2445268A1 (fr)
MX (1) MXPA03009796A (fr)
WO (1) WO2002088192A1 (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4559892B2 (ja) * 2005-03-28 2010-10-13 太陽インキ製造株式会社 着色感光性樹脂組成物及びその硬化物
JP4709619B2 (ja) * 2005-09-14 2011-06-22 富士フイルム株式会社 インク組成物
CN102282178B (zh) * 2009-01-14 2014-03-19 巴斯夫欧洲公司 液体光引发剂共混物
EP3074213B1 (fr) * 2013-11-26 2018-09-26 Novartis AG Dispersion d'oxyde métallique et ses utilisations
JP6068734B2 (ja) * 2014-12-10 2017-01-25 互応化学工業株式会社 液状ソルダーレジスト組成物及び被覆プリント配線板
KR101717115B1 (ko) * 2015-08-17 2017-03-16 한국단자공업 주식회사 전기적 연결용 버스바조립체

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH596241A5 (fr) * 1974-06-27 1978-03-15 Ciba Geigy Ag
EP0446175A3 (en) * 1990-03-09 1991-11-21 Ciba-Geigy Ag Mixture of photoinitiators
SG53043A1 (en) * 1996-08-28 1998-09-28 Ciba Geigy Ag Molecular complex compounds as photoinitiators

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO02088192A1 *

Also Published As

Publication number Publication date
WO2002088192A1 (fr) 2002-11-07
KR20040015181A (ko) 2004-02-18
MXPA03009796A (es) 2004-06-30
JP2004534117A (ja) 2004-11-11
CA2445268A1 (fr) 2002-11-07
CN1511166A (zh) 2004-07-07

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