Classifications

• • 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
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
  • B41M1/00—Inking and printing with a printer's forme
  • B41M1/02—Letterpress printing, e.g. book printing
  • B41M1/04—Flexographic printing
• • 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
  • C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
  • C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
  • C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
  • C08F236/06—Butadiene
• • 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
  • C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
• • 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
  • G03F7/032—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders
  • G03F7/033—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders the binders being polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
• • 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
  • G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
  • G03F7/0384—Macromolecular compounds which are rendered insoluble or differentially wettable with ethylenic or acetylenic bands in the main chain of the photopolymer
• • 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
  • G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
  • G03F7/0388—Macromolecular compounds which are rendered insoluble or differentially wettable with ethylenic or acetylenic bands in the side chains of the photopolymer
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41P—INDEXING SCHEME RELATING TO PRINTING, LINING MACHINES, TYPEWRITERS, AND TO STAMPS
  • B41P2200/00—Printing processes
  • B41P2200/10—Relief printing
  • B41P2200/12—Flexographic printing
• • 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
  • C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
  • C08F236/22—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having three or more carbon-to-carbon double bonds

Definitions

• the present invention relates to a photosensitive resin composition and a flexographic printing plate using the photosensitive resin composition.
• a photosensitive resin composition used for a flexographic printing plate generally contains a thermoplastic elastomer, a photopolymerizable unsaturated monomer, a plasticizer such as a conjugated diene rubber, and a photopolymerization initiator (for example, Patent Documents 1 to 4 ).
• a structure for a flexographic printing plate generally has a support made of a polyester film or the like, and a photosensitive layer made of the above photosensitive resin composition is provided thereon. If necessary, a slip layer or a protective layer is provided on the photosensitive layer for the purpose of smoothing the contact with the negative film.
• the entire surface is exposed to ultraviolet light through the support (back exposure) to form a thin uniform cured layer on the interface of the photosensitive layer with the support. Then, the surface of the photosensitive layer is subjected to image exposure (relief exposure) with ultraviolet light through a negative film covering the upper portion of the photosensitive layer. After that, the unexposed portion of the photosensitive layer is washed away with a developer, or after being heated and melted and then absorbed and removed by an absorbing layer, is subjected to post-processing exposure.
• a single negative film is usually used to form multiple printing plates. Since the photosensitive layer is generally tacky, if the negative film is placed directly on the photosensitive layer, the negative film stuck to the photosensitive layer will be damaged when the negative film is peeled off from the photosensitive layer after image exposure. may not be reused. Therefore, the photosensitive layer is required to have low tackiness so that the negative film can be easily peeled off and reused. However, the photosensitive layers using the photosensitive resin compositions described in Patent Documents 1 to 4 cannot sufficiently reduce the tackiness. In addition, the printing plate is also required to suppress adhesion of dust and breakage of the printed material during printing, and to have excellent printability. Further, the printing plate is also required to have little change in physical properties over time and to be excellent in printability stability.
• the first object of the present invention is to provide a photosensitive resin composition having low tackiness before and after curing and a low extraction rate after curing.
• a second object of the present invention is to provide a photosensitive resin composition with low tackiness before and after curing while maintaining a low extraction rate after curing.
• the present inventors have found that the problems can be solved by including a liquid farnesene rubber in the photosensitive resin composition, and have completed the present invention. That is, the present invention is as follows.
• a photosensitive resin composition comprising a thermoplastic elastomer (A), a liquid farnesene rubber (B), an ethylenically unsaturated compound (C), and a photoinitiator (D).
• the thermoplastic elastomer (A) is a styrene-butadiene-styrene block copolymer, a styrene-isoprene-styrene block copolymer, a styrene-(ethylene-butylene)-styrene block copolymer, and a styrene-( The photosensitive resin composition according to [1], which is at least one selected from the group consisting of ethylene-propylene)-styrene block copolymers.
• thermoplastic elastomer (A) is at least one selected from the group consisting of styrene-butadiene-styrene block copolymers and styrene-isoprene-styrene block copolymers [1] to [ 6].
• thermoplastic elastomer (A) contains a styrene-butadiene-styrene block copolymer.
• thermoplastic elastomer (A) contains a styrene-isoprene-styrene block copolymer.
• the content of the thermoplastic elastomer (A) is 40 to 87.9% by mass
• the content of the liquid farnesene rubber (B) is 10 to 40% by mass, based on the total amount of the photosensitive resin composition.
• the photosensitive resin composition according to any one of the above.
• a flexographic printing plate having a photosensitive layer comprising the photosensitive resin composition according to any one of [1] to [10] above.
• the photosensitive resin composition according to the present invention is characterized by containing a thermoplastic elastomer (A), a liquid farnesene rubber (B), an ethylenically unsaturated compound (C), and a photoinitiator (D).
• A thermoplastic elastomer
• B liquid farnesene rubber
• C ethylenically unsaturated compound
• D photoinitiator
• thermoplastic elastomer (A) used in the present invention is a polymer that can be plasticized and molded at a high temperature and exhibits properties as a rubber elastic body at room temperature.
• the thermoplastic elastomer (A) is not particularly limited, but is preferably a styrene-based block copolymer from the viewpoint of availability and moldability of the printing plate.
• a styrenic block copolymer is at least a polymer block mainly composed of structural units derived from styrene (hereinafter sometimes referred to as "polymer block (a)") and a polymer composed of structural units derived from a conjugated diene.
• polymer block (b) It is a block copolymer having blocks (hereinafter sometimes referred to as "polymer block (b)").
• the polymer block mainly composed of styrene-derived structural units preferably contains 90% by mass or more of styrene-derived structural units, more preferably 95% by mass or more, and still more preferably consists only of styrene-derived structural units.
• the polymer block mainly composed of structural units derived from styrene may contain structural units derived from styrenic monomers other than styrene.
• Styrenic monomers other than styrene include ⁇ -methylstyrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, pt-butylstyrene, 2,4-dimethylstyrene, vinylnaphthalene, and vinylanthracene. mentioned.
• examples of conjugated dienes in polymer blocks composed of structural units derived from conjugated dienes include butadiene, isoprene, chloroprene, 2,3-dimethylbutadiene, 1,3-pentadiene, and 1,3-hexadiene.
• butadiene and isoprene are preferable from the viewpoint of availability.
• One of the above monomers and conjugated dienes may be used alone, or two or more thereof may be used in combination.
• the olefinic double bond of the styrenic block copolymer is preferably not hydrogenated, but 10 mol% or less of the carbon-carbon double bonds of the structural units derived from the conjugated diene are hydrogenated. good too.
• the content of the polymer block (a) in the styrenic block copolymer is preferably 5% by mass or more, more preferably 10% by mass or more, from the viewpoint of effectively reducing tackiness. More preferably, it is 15% by mass or more, and from the viewpoint of moldability, it is preferably 50% by mass or less, more preferably 40% by mass or less, and 35% by mass or less. is more preferred.
• the content of the polymer block (b) in the styrene-based block copolymer is preferably 50% by mass or more, more preferably 60% by mass or more, and 65% by mass or more. is more preferably 95% by mass or less, more preferably 90% by mass or less, and even more preferably 85% by mass or less.
• thermoplastic elastomer (A) examples include styrene-butadiene-styrene block copolymer (SBS), styrene-isoprene-styrene block copolymer (SIS), styrene-(ethylene-butylene)-styrene block copolymer. coalesced (SEBS), styrene-(ethylene-propylene)-styrene block copolymer (SEPS), and the like.
• SBS styrene-butadiene-styrene block copolymer
• SIS styrene-isoprene-styrene block copolymer
• SEBS styrene-(ethylene-butylene)-styrene block copolymer
• SEPS styrene-(ethylene-propylene)-styrene block copolymer
• thermoplastic elastomer (A) is at least selected from the group consisting of styrene-butadiene-styrene block copolymers and styrene-isoprene-styrene block copolymers.
• One type is preferred.
• thermoplastic elastomer (A) comprises a styrene-butadiene-styrene block copolymer.
• thermoplastic elastomer (A) comprises a styrene-isoprene-styrene block copolymer.
• the thermoplastic elastomer (A) may contain a styrene-butadiene-styrene block copolymer and a styrene-isoprene-styrene block copolymer.
• the thermoplastic elastomer (A) may also be a styrene-butadiene-styrene block copolymer and a styrene-butadiene/isoprene-styrene block copolymer.
• butadiene/isoprene means a copolymer block containing butadiene and isoprene as constituent monomers.
• thermoplastic elastomers examples include “Kraton D” (trade name) manufactured by Kraton Polymer Co., Ltd., and “Tufprene (registered trademark)” (trade name) and Asaprene (registered trademark) manufactured by Asahi Kasei Chemicals Corporation. Trademark) T” (trade name), “JSR TR” (trade name) and “JSR SIS” (trade name) manufactured by JSR Corporation, and "Quintac (registered trademark)” (trade name) manufactured by Zeon Corporation. , "Hibller 5125" (trade name) and “Hiblr 5127” (trade name) manufactured by Kuraray Co., Ltd., and the like.
• the weight average molecular weight (Mw) of the thermoplastic elastomer (A) is not particularly limited, but is preferably 10,000 to 1,000,000, more preferably 50,000 to 400,000, and still more preferably. is between 80,000 and 250,000, even more preferably between 80,000 and 200,000.
• Mw of the thermoplastic elastomer (A) is 10,000 or more, the mechanical strength of the printing plate can be enhanced, and when it is 1,000,000 or less, the moldability of the printing plate can be enhanced.
• the Mw of the thermoplastic elastomer (A) is 10,000 or more, the mechanical strength of the printing plate can be enhanced, and when it is 1,000,000 or less, the moldability of the printing plate can be enhanced.
• the weight average molecular weight in this specification is the weight average molecular weight of polystyrene conversion measured by the gel permeation chromatography (GPC).
• the vinyl content of the polymer block composed of structural units derived from the conjugated diene of the thermoplastic elastomer (A) is preferably 1 to 50 mol%, more preferably 5 to 50 mol%, from the viewpoint of curability of the composition. , more preferably 5 to 40 mol %, still more preferably 5 to 30 mol %, particularly preferably 10 to 30 mol %. Further, the vinyl content is preferably 40 to 80 mol%, more preferably 50 to 80 mol%, still more preferably 50 to 75 mol%, from the viewpoint of cold flow resistance of the composition. .
• the content of the thermoplastic elastomer (A) is preferably 40 to 87.9% by mass, more preferably 50 to 85% by mass, still more preferably 60 to 80% by mass, based on the total amount of the photosensitive resin composition. % by mass.
• the content of the thermoplastic elastomer (A) is 40% by mass or more, the tackiness of the composition before and after curing can be further reduced, and when it is 87.9% by mass or less, the flexibility of the composition is increased. can be done.
• the liquid farnesene rubber (B) used in the present invention is a rubber that can be handled in a liquid state.
• the term “liquid” means that the liquid farnesene rubber (B) has a melt viscosity of 0.1 to 4,000 Pa ⁇ s measured at 38°C.
• the melt viscosity is preferably 1 to 2,000 Pa ⁇ s, more preferably 2 to 1,000 Pa ⁇ s, still more preferably 10 to 750 Pa ⁇ s, and even more preferably 10 to 500 Pa ⁇ s.
• the melt viscosity is preferably 0.3 to 2,000 Pa s, more preferably 0.5 to 1,000 Pa s, still more preferably 0.7 to 750 Pa s, and 0.7 to 500 Pa • s is even more preferred.
• the melt viscosity of the liquid farnesene rubber (B) is a value measured at 38°C with a Brookfield viscometer.
• the liquid farnesene-based rubber (B) is a liquid polymer containing farnesene-derived monomer units (a) (hereinafter sometimes simply referred to as "monomer units (a)").
• the monomer unit (a) may be a monomer unit derived from ⁇ -farnesene, or may be a monomer unit derived from ⁇ -farnesene represented by the following formula (I), although it may contain a monomer unit derived from ⁇ -farnesene and a monomer unit derived from ⁇ -farnesene, it preferably contains a monomer unit derived from ⁇ -farnesene from the viewpoint of ease of production.
• the content of the ⁇ -farnesene-derived monomer unit is preferably 80 mol% or more, more preferably 90 mol% or more, still more preferably 100 mol, in the monomer unit (a) from the viewpoint of ease of production. %, ie all of the monomeric units (a) are ⁇ -farnesene-derived monomeric units.
• the content of the monomer unit (a) in the liquid farnesene rubber (B) is preferably 10% by mass or more, more preferably 10% by mass or more, from the viewpoint of further reducing the curability of the composition and the tackiness before and after curing. It is 30% by mass or more, more preferably 50% by mass or more.
• the upper limit of the content of the monomer unit (a) in the liquid farnesene rubber (B) is not particularly limited, and may be 100% by mass, less than 100% by mass, 99% by mass or less, 90% by mass. % or less, or 80% by mass or less.
• the liquid farnesene rubber (B) contains other monomer units, and the content of the monomer units (a) is less than 100% by mass, preferably 99% by mass or less.
• the content of the monomer units (a) in the liquid farnesene rubber (B) is 100% by mass.
• the liquid farnesene rubber (B) comprises a monomer unit (a) and a monomer unit (b) derived from a monomer other than farnesene (hereinafter simply referred to as "monomer unit (b)"). It may be a liquid copolymer containing.
• the content of the monomer unit (b) in the liquid farnesene rubber (B) is preferably 10 to 90% by mass, more preferably 20 to 70% by mass, and still more preferably 20 to 50% by mass.
• the glass transition temperature can be lowered, and when it is 90% by mass or less, the viscosity is lowered and handleability is reduced. can be improved.
• a monomer other than farnesene that can form the liquid farnesene-based rubber (B) is not particularly limited as long as it is copolymerizable with farnesene.
• Other monomers than farnesene include, for example, aromatic vinyl compounds, conjugated diene compounds other than farnesene, acrylic acid and its derivatives, methacrylic acid and its derivatives, acrylamide and its derivatives, methacrylamide and its derivatives, and acrylonitrile. is mentioned. These monomers other than farnesene may be used singly or in combination of two or more.
• aromatic vinyl compound examples include styrene, ⁇ -methylstyrene, 2-methylstyrene, 3-methylstyrene, 4-methylstyrene, 4-propylstyrene, 4-t-butylstyrene, 4-cyclohexylstyrene, 4- Dodecylstyrene, 2,4-dimethylstyrene, 2,4-diisopropylstyrene, 2,4,6-trimethylstyrene, 2-ethyl-4-benzylstyrene, 4-(phenylbutyl)styrene, N,N-diethyl-4 -Styrene derivatives such as aminoethylstyrene, 4-methoxystyrene, monochlorostyrene and dichlorostyrene; 1-vinylnaphthalene, 2-vinylnaphthalene, vinylanthracene, vinylpyridine and the like
• conjugated diene compounds examples include butadiene, isoprene, 2,3-dimethylbutadiene, 2-phenylbutadiene, 1,3-pentadiene, 2-methyl-1,3-pentadiene, 1,3-hexadiene, and 1,3-octadiene. , 1,3-cyclohexadiene, 2-methyl-1,3-octadiene, 1,3,7-octatriene, myrcene, chloroprene and the like. Among these, butadiene, isoprene and myrcene are preferred, and butadiene is more preferred. These conjugated dienes may be used singly or in combination of two or more.
• Examples of derivatives of acrylic acid include methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, t-butyl acrylate, 2-ethylhexyl acrylate, isooctyl acrylate, isononyl acrylate, lauryl acrylate, Stearyl acrylate, cyclohexyl acrylate, isobornyl acrylate, dicyclopentenyloxyethyl acrylate, tetraethylene glycol acrylate, tripropylene glycol acrylate, 4-hydroxybutyl acrylate, 3-hydroxy-1-adamantyl acrylate, acrylic tetrahydrofurfuryl acid, methoxyethyl acrylate, N,N-dimethylaminoethyl acrylate and the like.
• One of these acrylic acid derivatives may be used alone, or two or more thereof may be used in combination.
• methacrylic acid derivatives examples include methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, t-butyl methacrylate, 2-ethylhexyl methacrylate, lauryl methacrylate, tridecyl methacrylate, stearyl methacrylate, Cyclohexyl methacrylate, isobornyl methacrylate, dicyclopentanyl methacrylate, benzyl methacrylate, dicyclopentenyloxyethyl methacrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 3-hydroxy-1-adamantyl methacrylate , tetrahydrofurfuryl methacrylate, dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate, glycidyl methacrylamide methacrylate, and the
• acrylamide derivatives examples include dimethylacrylamide, acryloylmorpholine, isopropylacrylamide, diethylacrylamide, dimethylaminopropylacrylamide, dimethylaminopropylacrylamide methyl chloride quaternary salt, hydroxyethylacrylamide, 2-acrylamido-2-methylpropanesulfonic acid and the like. mentioned. These acrylamide derivatives may be used singly or in combination of two or more.
• methacrylamide derivatives examples include dimethylmethacrylamide, methacryloylmorpholine, isopropylmethacrylamide, diethylmethacrylamide, dimethylaminopropylmethacrylamide, and hydroxyethylmethacrylamide.
• One of these methacrylamide derivatives may be used alone, or two or more thereof may be used in combination.
• aromatic vinyl compounds and conjugated diene compounds other than farnesene are preferred, and conjugated diene compounds other than farnesene are more preferred.
• the number average molecular weight (Mn) of the liquid farnesene rubber (B) is preferably 10,000 to 150,000, more preferably 20,000 to 100,000, still more preferably 25,000 to 80, 000. When the Mn of the liquid farnesene rubber (B) is 10,000 or more, the curability of the composition can be improved and the tackiness before and after curing can be further reduced. Excellent in nature. In another embodiment, the number average molecular weight (Mn) of the liquid farnesene rubber (B) is preferably 7,000 to 150,000, more preferably 8,000 to 100,000, and still more preferably 8,500 to 80,000. When the Mn of the liquid farnesene rubber (B) is 7,000 or more, the curability of the composition can be improved and the tackiness before and after curing can be further reduced. Excellent in nature.
• the molecular weight distribution (Mw/Mn) of the liquid farnesene rubber (B) is not particularly limited, but is preferably 1.0 to 2.0, more preferably 1.0 to 1.5, and further It is preferably 1.0 to 1.2, and more preferably 1.0 to 1.1.
• Mw/Mn of the liquid farnesene rubber (B) is within the above range, it is possible to suppress fluctuations in curability and tackiness of the composition.
• the number average molecular weight and molecular weight distribution of the liquid farnesene rubber (B) are based on polystyrene conversion obtained by GPC measurement according to the method described in Examples described later.
• the glass transition temperature (Tg) of the liquid farnesene rubber (B) depends on the bonding mode (microstructure), the farnesene-derived monomeric unit (a), and other monomeric units other than farnesene (although it may vary depending on the content of b), it is preferably -65°C or lower, more preferably -70°C or lower, and still more preferably -75°C or lower. If the Tg of the liquid farnesene rubber (B) is ⁇ 65° C. or lower, the composition of the present invention can be expected to improve the high-speed printability of the printing plate.
• the lower limit of the Tg of the liquid farnesene rubber (B) is not particularly limited, but is preferably -100°C or higher, more preferably -90°C or higher, and still more preferably -85°C or higher. .
• the glass transition temperature (Tg) of the liquid farnesene rubber (B) is preferably ⁇ 60° C. or lower, more preferably ⁇ 65° C. or lower, and still more preferably ⁇ 70° C. or lower. , ⁇ 75° C. or lower. If the Tg of the liquid farnesene rubber (B) is ⁇ 60° C. or lower, the composition of the present invention can be expected to improve the high-speed printability of the printing plate.
• the lower limit of the Tg of the liquid farnesene rubber (B) is not particularly limited, but is preferably -100°C or higher, more preferably -90°C or higher, and still more preferably -85°C or higher. .
• the Tg of the liquid farnesene rubber (B) is determined by differential scanning calorimetry, more specifically, by the method described in Examples below.
• the vinyl content of the monomer unit (a) of the liquid farnesene rubber (B) is preferably 0.5 to 70 from the viewpoint of the curability of the composition and the high-speed printability of the printing plate derived from the Tg described above. mol%, more preferably 1 to 60 mol%, still more preferably 1 to 50 mol%, even more preferably 1 to 40 mol%, still more preferably 3 to 30 mol% , particularly preferably 5 to 15 mol %.
• the term “vinyl content of the monomer unit (a)” refers to the content of the bonding mode excluding the 1,13 bond such as the following formula (II) among the farnesene-derived monomer units. is.
• the vinyl content of the liquid farnesene rubber (B) is preferably 5 to 80 mol%, more preferably 5 to 80 mol%, from the viewpoint of curability of the composition and high-speed printability of the printing plate derived from the above Tg. It is 60 mol %, more preferably 5 to 50 mol %, still more preferably 5 to 45 mol %.
• the “vinyl content of the liquid farnesene rubber (B)” refers to the vinyl content of the farnesene-derived monomeric unit (a) and the vinyl content of the monomeric unit (b) other than farnesene. means total.
• the vinyl content of the liquid farnesene-based rubber (B) is obtained by calculating the vinyl content of each of the farnesene-derived monomer units (a) and of the monomer units (b) other than farnesene, and summing them up. is required.
• the vinyl content of the farnesene-derived monomeric unit (a) and the vinyl content of the monomeric unit (b) other than farnesene are each measured by the method using 1 H-NMR described in Examples below. can.
• the content of the liquid farnesene rubber (B) is preferably 10 to 40% by mass, more preferably 10 to 35% by mass, still more preferably 10 to 30% by mass, relative to the total amount of the photosensitive resin composition. %.
• the content of the liquid farnesene rubber (B) is 10% by mass or more, the viscosity of the composition during molding can be lowered to improve the processability, and the flexibility of the resulting molded article can be improved.
• the molded article can preferably be used as a printing plate.
• the content of the liquid farnesene rubber (B) is 40% by mass or less, the tackiness before and after curing of the molded article obtained by molding the composition can be further reduced. Such properties are particularly emphasized in embodiments in which the molded article is used as a printing plate.
• the ethylenically unsaturated compound (C) used in the present invention includes esters such as acrylic acid, methacrylic acid, fumaric acid and maleic acid, acrylamide and methacrylamide derivatives, allyl esters, styrene and its derivatives, N-substituted maleimide compounds, and the like. is mentioned.
• alkanediols such as hexanediol and nonanediol, ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, polyethylene glycol, butylene glycol diacrylates and dimethacrylates, and trimethylol.
• alkanediol di(meth)acrylates are preferable as the ethylenically unsaturated compound (C) from the viewpoint of curability.
• the content of the ethylenically unsaturated compound (C) is preferably 2 to 30% by mass, more preferably 2 to 20% by mass, and still more preferably 3 to 15% by mass, based on the total amount of the photosensitive resin composition. % by mass.
• the content of the ethylenically unsaturated compound (C) is 2% by mass or more, the curability is improved, and the formation of fine dots and characters on the printing plate can be improved. can improve sexuality.
• Photoinitiator (D) As the photoinitiator (D) used in the present invention, known photoinitiators such as aromatic ketones and benzoin ethers can be used. Propiophenone, diethoxyacetophenone, 1-(4-isopropylphenyl)-2-hydroxy-2-methylpropanone, 1-(4-dodecylphenyl)-2-hydroxy-2-methylpropanone, 4-(2 -hydroxyethoxy)-phenyl(2-hydroxy-2-propyl)ketone, 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropanone, benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin-n-butyl ether, benzoin phenyl ether, benzyl dimethyl ketal, benzophenone, benzoylbenzoic acid, methyl benzoylbenzoate, 4-phenylbenzo
• a photoinitiator (D) may be used individually by 1 type, and may use 2 or more types together. Among them, benzyl dimethyl ketal, diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide, and phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide are preferred, and benzyl dimethyl ketal is more preferred, from the viewpoint of curability.
• photoinitiator (D) for example, trade names “Irgacure 184", “Irgacure 127", “Irgacure 149", “Irgacure 261", “Irgacure 369", “Irgacure 500", “Irgacure 651”, “Irgacure 754", “Irgacure 784", “Irgacure 819", “Irgacure 907", “Irgacure 1116", “Irgacure 1173”, “Irgacure 1664”, “Irgacure 1700", “Irgacure 1800”, “Irgacure 1850”, Commercially available products such as “Irgacure 2959”, “Irgacure 4043”, “Darocure (registered trademark; hereinafter abbreviated) 1173", and “Darocure MBF” (manufactured by BASF) are preferably used
• the content of the photoinitiator (D) is preferably 0.1-10% by mass, more preferably 0.5-5% by mass, relative to the total amount of the photosensitive resin composition.
• the content of the photoinitiator (D) is 0.1% by mass or more, it is possible to improve the formability of fine dots and characters on the printing plate, and when it is 10% by mass or less, the transmission of active light such as ultraviolet rays. rate can be improved.
• the photosensitive resin composition of the present invention comprises the thermoplastic elastomer (A), the liquid farnesene rubber (B), the ethylenically unsaturated compound (C), and the photoinitiator (D), as well as an antioxidant. , plasticizers, fillers, colorants, thermal polymerization inhibitors, UV absorbers, antihalation agents, light stabilizers and the like.
• the content of the above-mentioned other components is not particularly limited as long as it does not impair the effects of the present invention. It is 5 to 40% by mass, more preferably 0.5 to 30% by mass.
• the total content of the thermoplastic elastomer (A), the liquid farnesene rubber (B), the ethylenically unsaturated compound (C), and the photoinitiator (D) is preferably 85% by mass or more, more preferably 90% by mass or more, still more preferably 95% by mass or more, may be 100% by mass or less, may be 98% by mass or less, or may be 96% by mass or more. % by mass or less.
• the method for producing the photosensitive resin composition of the present invention is not particularly limited, and the thermoplastic elastomer (A), the liquid farnesene rubber (B), the ethylenically unsaturated compound (C), the photoinitiator (D), and the above A method capable of uniformly mixing the other components can be preferably employed.
• a method of melt-kneading using a single-screw extruder, twin-screw extruder, kneader, Banbury mixer, or the like is preferably adopted.
• the kneading temperature is preferably 100-200°C, more preferably 120-180°C.
• the photosensitive resin composition after kneading can be formed into a sheet having a desired thickness by calender roll, press, extrusion molding, or the like.
• the temperature during molding is preferably 100 to 200°C, more preferably 120 to 180°C.
• the photosensitive resin composition of the present invention can also be used as a layer constituting a laminate.
• the photosensitive resin composition of the present invention preferably exhibits a tendency of low tackiness before curing as compared with a photosensitive resin composition containing a comparable liquid farnesene rubber (B) substitute.
• a photosensitive resin composition containing a comparable liquid farnesene rubber (B) substitute Such low tackiness before curing allows the negative film to be easily peeled off after imagewise exposure even if the negative film is placed directly on the photosensitive layer made of the photosensitive resin composition, and the negative film can be easily peeled off. Reuse becomes possible.
• the photosensitive resin composition of the present invention preferably exhibits a tendency of low tackiness after curing as compared with a photosensitive resin composition containing a liquid farnesene rubber (B) substitute which can be compared. .
• Such low tackiness after curing suppresses tackiness of the flexographic printing plate having a photosensitive layer made of a photosensitive resin composition, suppresses adhesion of dust during printing and tearing of the printed material, and improves printability.
• Excellent for The tackiness of the photosensitive resin composition before and after curing can be measured by the method described in Examples.
• the photosensitive resin composition has a tackiness at 25° C. before curing of preferably 9.5 N or less, more preferably 7.5 N or less, still more preferably 6.5 N or less, Even more preferably, it is 6.0N or less, and particularly preferably 5.5N or less.
• the thermoplastic elastomer (A) preferably contains a styrene-butadiene-styrene block copolymer, more preferably the thermoplastic elastomer (A) contains styrene -Butadiene-styrene block copolymer, and the liquid farnesene rubber (B) contains monomer units (a) and monomer units (b).
• the lower limit of tackiness at 25° C. before curing is not particularly limited, but is, for example, 0.1 N or more.
• the tackiness at 25° C. before curing is 9.5 N or less, the above-mentioned effects are exhibited more remarkably.
• the photosensitive resin composition according to one embodiment described above has a tackiness at 25° C. after curing of preferably 3.0 N or less, more preferably 2.5 N or less, and still more preferably 2.0 N. It is below.
• the lower limit of the tackiness at 25° C. after curing is not particularly limited, but is, for example, 0.1 N or more. When the tackiness at 25° C. after curing is 3.0 N or less, the above-mentioned effects are exhibited more remarkably.
• the photosensitive resin composition according to another embodiment preferably has a tackiness at 25°C before curing of less than 14.3N, more preferably 13.5N or less, and still more preferably 13.3N or less.
• the thermoplastic elastomer (A) preferably contains a styrene-isoprene-styrene block copolymer, more preferably the thermoplastic elastomer (A) is A styrene-isoprene-styrene block copolymer is included, and the content of the monomer unit (a) in the liquid farnesene rubber (B) is 100% by mass.
• the lower limit of tackiness at 25° C. before curing is not particularly limited, but is, for example, 0.1 N or more. When the tackiness at 25° C. before curing is less than 14.3 N, the above-mentioned effects are exhibited more remarkably.
• the photosensitive resin composition according to another embodiment described above preferably has a tackiness at 25° C. after curing of less than 6.3N, more preferably 6.2N or less, and still more preferably 6.2N or less. 1N or less.
• the lower limit of the tackiness at 25° C. after curing is not particularly limited, but is, for example, 0.1 N or more. When the tackiness at 25° C. after curing is less than 6.3 N, the above-mentioned effects are exhibited more remarkably.
• the cured product of the photosensitive resin composition of the present invention preferably exhibits a tendency of a low component extraction rate with respect to a solvent such as toluene. Due to such a low extraction rate, a flexographic printing plate having a photosensitive layer made of such a photosensitive resin composition is excellent in printability stability because changes in physical properties over time are suppressed. For example, it can be expected to have excellent long-run properties when used for a long time and storage stability when stored for a long period of time. More preferably, the cured product of the photosensitive resin composition of the present invention tends to exhibit a low component extraction rate with respect to a solvent such as toluene, while exhibiting a tendency of low tackiness before and after curing as described above.
• the extraction rate of the liquid farnesene rubber (B) from the cured product of the photosensitive resin composition can be measured by the method described in Examples.
• the cured product of the photosensitive resin composition according to one embodiment described above preferably has an extraction rate of the liquid farnesene rubber (B) after being immersed in toluene at 25° C. for 48 hours, and is preferably 15.0% by mass or less. It is more preferably 10.0% by mass or less, and still more preferably 8.0% by mass or less. When the extraction rate is 15.0% by mass or less, the above-mentioned effects are exhibited more remarkably.
• the cured product of the photosensitive resin composition according to another embodiment described above preferably has an extraction rate of 20.0% by mass or less of the liquid farnesene rubber (B) after being immersed in toluene at 25° C. for 48 hours. , more preferably 19.0% by mass or less, and still more preferably 18.0% by mass or less.
• the extraction rate is 20.0% by mass or less
• the cured product of the photosensitive resin composition according to this another embodiment tends to have a low extraction rate, while the tackiness before and after curing described above is low. It tends to be possible to achieve the above-described effect of showing the tendency of
• the cured product of the photosensitive resin composition of the present invention preferably has a glass transition temperature (Tg) of showing a tendency to be low. With such a low glass transition temperature (Tg), flexographic printing plates having a photosensitive layer made of such a photosensitive resin composition can be expected to have improved high-speed printing properties.
• Tg of the cured product of the photosensitive resin composition can be measured by the method described in Examples.
• the cured product of the photosensitive resin composition according to one embodiment described above preferably has a glass transition temperature (Tg) of ⁇ 80° C. or less, more preferably ⁇ 84° C. or less, and even more preferably ⁇ 86° C. or less. is.
• Tg glass transition temperature
• the cured product of the photosensitive resin composition according to another embodiment described above preferably has a glass transition temperature (Tg) of -57°C or lower, more preferably -59°C or lower, and still more preferably -61°C. It is below.
• Tg glass transition temperature
• the flexographic printing plate of the present invention has a photosensitive layer comprising the above photosensitive resin composition.
• the sheet of the photosensitive resin composition is placed on the support, and the sheet of the photosensitive resin composition is adhered to the support by roll lamination, and then hot pressed to form a photosensitive layer on the support.
• a construction for a flexographic printing plate can be obtained.
• the thickness of the photosensitive layer is usually 0.5 to 7 mm, preferably 0.5 to 3.5 mm.
• the thickness of the printing plate is usually 0.5 to 7.0 mm, preferably 0.5 to 3.5 mm.
• the thickness of the printing plate can be varied depending on the substrate to be printed. When it is necessary to reduce the thickness of the printing plate according to the material to be printed, for example, when it is required to be 3.0 mm or less, the blending amount of each component in the photosensitive resin composition is changed.
• the thermoplastic elastomer (A) in the photosensitive resin composition may contain a styrene-isoprene-styrene block copolymer.
• the hardness of the printing plate is generally 28-74, preferably 30-65, of type A hardness.
• the hardness of the printing plate can be measured with a type A hardness tester according to JIS K6253-3:2012.
• the hardness of the printing plate can be varied depending on the substrate to be printed. When it is necessary to increase the hardness of the printing plate according to the substrate to be printed, for example, when the type A hardness is required to be 60 or more in accordance with the thickness of the printing plate being 3.0 mm or less.
• thermoplastic elastomer (A) is styrene - isoprene-styrene block copolymer.
• the alternative embodiment described above is particularly suitable when the printing plate has a small thickness and a high hardness.
• a flexographic printing plate from a flexographic printing plate structure As a general method for making a flexographic printing plate from a flexographic printing plate structure, first, the entire surface is exposed to ultraviolet rays through the support (back exposure), and a thin uniform hardening layer is formed on the interface between the support and the photosensitive layer. Subsequently, the surface of the photosensitive layer is subjected to imagewise exposure (relief exposure) with ultraviolet rays through a negative film covering the upper portion of the photosensitive layer. After that, the unexposed portion of the photosensitive layer is washed away with a developer, or after being heated and melted and then absorbed and removed by an absorbing layer, is subjected to post-processing exposure.
• the imagewise exposure for changing the surface tension of the plate surface it may be exposed to ultraviolet rays in the wavelength range of 310 to 400 nm after exposure to ultraviolet rays in the wavelength range of 200 to 300 nm. Either the exposure from the negative film side (relief exposure) or the exposure from the support side (back exposure) may be performed first, or both may be performed at the same time.
• Examples of the exposure light source include high pressure mercury lamps, ultraviolet fluorescent lamps, carbon arc lamps, xenon lamps and diode lamps.
• Examples of developing solvents used for developing unexposed areas include esters such as heptyl acetate and 3-methoxybutyl acetate, hydrocarbons such as petroleum fractions, toluene and decalin, and chlorinated organic solvents such as tetrachlorethylene. and mixtures of alcohols such as propanol, butanol and pentanol.
• the unexposed areas are washed out with the developing solvent by spraying from a nozzle or by brushing with a brush.
• a method of irradiating the surface with light having a wavelength of 300 nm or less is common. If necessary, light larger than 300 nm may be used together.
• Liquid polybutadiene Liquid polybutadiene (b-1): liquid polybutadiene (b-1) produced in Production Example 4 described later Liquid polybutadiene (b-2): liquid polybutadiene (b-2) produced in Production Example 5 described later Liquid polybutadiene (b-3): liquid polybutadiene (b-3) produced in Production Example 6 described later
• Ethylenically unsaturated compound (C) Ethylenically unsaturated compound (C-1): HDDA (trade name, manufactured by Tokyo Chemical Industry Co., Ltd., 1,6-hexanediol diacrylate)
• Antioxidant BHT (trade name, manufactured by Kawaguchi Chemical Industry Co., Ltd., dibutyl hydroxytoluene)
• ⁇ -farnesene (purity 97.6% by mass, manufactured by Amyris Biotechnology) was purified with 3 ⁇ molecular sieves and distilled under a nitrogen atmosphere to give zingiberene, bisabolene, farnesene epoxide, farnesol isomer, E, ⁇ -Farnesene was purified by removing hydrocarbon impurities such as E-farnesol, squalene, ergosterol and some dimers of farnesene.
• Liquid polyfarnesene-butadiene copolymer (B-1) 1140 g of cyclohexane as a solvent and 56.2 g of sec-butyllithium (10.5% by mass cyclohexane solution) as a polymerization initiator were placed in a pressure vessel that had been purged with nitrogen and dried. of ⁇ -farnesene and 720 g of butadiene was added and polymerized for 1 hour. The obtained polymerization reaction liquid was treated with methanol, and water was used to wash the polymerization reaction liquid. The polymerization reaction solution after washing and water are separated and dried at 70° C. for 12 hours to obtain a liquid polyfarnesene-butadiene copolymer which is a random copolymer containing 60% by mass of farnesene units and 40% by mass of butadiene units. Combined (B-1) was produced.
• Liquid polyfarnesene-butadiene copolymer (B-2) 267 g of cyclohexane as a solvent and 7.4 g of sec-butyllithium (10.5% by mass cyclohexane solution) as a polymerization initiator were placed in a pressure vessel that had been purged with nitrogen and dried. of ⁇ -farnesene and 240 g of butadiene was added and polymerized for 2 hours. The obtained polymerization reaction liquid was treated with methanol, and water was used to wash the polymerization reaction liquid. After washing, the polymerization reaction solution and water are separated and dried at 70° C. for 12 hours to obtain a liquid polyfarnesene-butadiene copolymer, which is a random copolymer containing 40% by mass of farnesene units and 60% by mass of butadiene units. Combined (B-2) was produced.
• Liquid polyfarnesene-butadiene copolymer (B-3) 267 g of cyclohexane as a solvent and 9.3 g of sec-butyllithium (10.5% by mass cyclohexane solution) as a polymerization initiator were placed in a pressure vessel that had been purged with nitrogen and dried. of ⁇ -farnesene and 320 g of butadiene was added and polymerized for 2 hours. The obtained polymerization reaction liquid was treated with methanol, and water was used to wash the polymerization reaction liquid. After washing, the polymerization reaction solution and water are separated and dried at 70° C. for 12 hours to obtain a liquid polyfarnesene-butadiene copolymer which is a random copolymer containing 20% by mass of farnesene units and 80% by mass of butadiene units. Combined (B-3) was produced.
• Liquid polybutadiene (b-1) 400 g of hexane as a solvent and 48.4 g of n-butyllithium (17 mass% hexane solution) as an initiator are charged in a pressure vessel that has been purged with nitrogen and dried, and N,N,N',N'-tetramethyl as a polar compound. After charging 5.4 g of ethylenediamine and raising the temperature to 50° C., 400 g of butadiene was added and polymerized for 1 hour. The obtained polymerization reaction liquid was treated with methanol, and water was used to wash the polymerization reaction liquid. After washing, the polymerization reaction solution and water were separated and dried at 70° C. for 12 hours to produce liquid polybutadiene (b-1).
• Liquid polyfarnesene (B-4) 400 g of cyclohexane as a solvent and 29.8 g of sec-butyllithium (10.5% by mass cyclohexane solution) as a polymerization initiator were placed in a pressure vessel that had been purged with nitrogen and dried. of ⁇ -farnesene was added and polymerized for 2 hours. The obtained polymerization reaction liquid was treated with methanol, and water was used to wash the polymerization reaction liquid. After washing, the polymerization reaction solution and water were separated and dried at 70° C. for 12 hours to produce a liquid polyfarnesene (B-4).
• Mw Weight average molecular weight
• Mn number average molecular weight
• Mw/Mn molecular weight distribution
• GPC apparatus GPC apparatus "GPC8020” manufactured by Tosoh Corporation ⁇ Separation column: “TSKgelG4000HXL” manufactured by Tosoh Corporation ⁇ Detector: “RI-8020” manufactured by Tosoh Corporation ⁇ Eluent: Tetrahydrofuran ⁇ Eluent flow rate: 1.0 ml/min ⁇ Sample concentration: 5 mg/10 ml ⁇ Column temperature: 40°C
• Glass transition temperature (Tg) 10 mg of the liquid polymer was placed in an open aluminum pan, covered with an aluminum lid, and crimped with a sample sealer. A thermogram was measured by differential scanning calorimetry (DSC) at a heating rate of 10°C/min, and the peak top value of DDSC was taken as the glass transition temperature (Tg).
• the measuring equipment and conditions are as follows. [Measurement device and measurement conditions] ⁇ Apparatus: Differential scanning calorimeter "DSC6200" manufactured by Seiko Instruments Inc. ⁇ Cooling device: Cooling controller manufactured by Seiko Instruments Inc.
• ⁇ Detector Heat flux type ⁇ Sample weight: 10 mg ⁇ Temperature increase rate: 10°C/min ⁇ Cooling condition: 10°C/min After cooling, the temperature was maintained isothermally at -130°C for 3 minutes, and the temperature increase was started. ⁇ Reference container: aluminum ⁇ Reference weight: 0 mg
• melt viscosity (38°C) The melt viscosity of the liquid polymer at 38° C. was measured with a Brookfield viscometer (manufactured by BROOKFIELD ENGINEERING LABS. INC.).
• the obtained uncured sheet was irradiated with ultraviolet rays using a UV irradiator (manufactured by Heraeus; mercury xenon lamp) at an illuminance of 500 mJ/cm 2 and an integrated light amount of 8000 mJ/cm 2 .
• a sheet (hereinafter also referred to as a cured sheet) having a thickness of 2 mm was obtained.
• Tackiness An uncured sheet and a cured sheet were cut into a size of 2 cm x 10 cm. The uncured sheet and the cover sheet of the cured sheet are peeled off, and the stainless steel plate, the uncured sheet, and the surface of the cured sheet are moved at a speed of 10 mm/min using a Picmatac tester (manufactured by Toyo Seiki Co., Ltd.) as a measuring device. After contacting for 4 seconds, the tackiness (stickiness) was measured by peeling the uncured sheet and the cured sheet vertically from the surface of the stainless steel plate at a speed of 10 mm/min.
• a Picmatac tester manufactured by Toyo Seiki Co., Ltd.
• Glass transition temperature (Tg) 10 mg of the cured sheet was placed in an open aluminum pan, covered with an aluminum lid, and crimped with a sample sealer.
• a thermogram was measured by differential scanning calorimetry (DSC) at a heating rate of 10°C/min, and the peak top value of DDSC was taken as the glass transition temperature (Tg).
• DSC differential scanning calorimetry
• Tg glass transition temperature
• the photosensitive resin compositions of Examples 1-1 to 1-5 have low tackiness before and after curing, a low extraction rate of the liquid polymer after curing, and a glass transition temperature of the sheet after curing. I know it's low.
• the obtained uncured sheet was irradiated with ultraviolet rays using a UV irradiator (manufactured by Heraeus; mercury xenon lamp) at an illuminance of 500 mJ/cm 2 and an integrated light amount of 8000 mJ/cm 2 .
• a sheet (cured sheet) having a thickness of 2 mm was obtained.
• the photosensitive resin compositions of Examples 2-1 and 2-2 can provide a photosensitive resin composition with low tackiness before and after curing while maintaining a low extraction rate after curing. I understand. Further, from Table 3, it can be seen that the photosensitive resin compositions of Examples 2-1 and 2-2 also have low glass transition temperatures of the cured sheets.
• the photosensitive resin composition of the present invention has low tackiness before curing, even if a negative film is placed directly on the photosensitive layer composed of the photosensitive resin composition, the negative film can be easily peeled off after image exposure. and the negative film can be reused.
• the photosensitive resin composition of the present invention has low tackiness after curing, a printing plate having a photosensitive layer made of the photosensitive resin composition is less sticky, and is free from adhesion of dust and dirt during printing. Excellent printability because tearing of printed matter is suppressed.
• the photosensitive resin composition of the present invention tends to have a low extraction rate of the liquid polymer after curing. Since it is suppressed, it is excellent in printability stability. Therefore, the photosensitive resin composition of this embodiment is suitably used for flexographic printing plates.

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• 2022
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