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
  • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
  • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
  • C08F220/10—Esters
  • C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
  • C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
• • 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
  • C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
• • 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
  • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
  • C09D133/04—Homopolymers or copolymers of esters
  • C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
  • C09D133/062—Copolymers with monomers not covered by C09D133/06
  • C09D133/066—Copolymers with monomers not covered by C09D133/06 containing -OH groups

Definitions

• Patent Document 1 describes a medical device in which a surface layer made of a cured product of a compound having a biocompatible group and an alkoxysilyl group is provided on at least a portion of the surface of a device base material.
• a copolymer having a unit based on (meth)acrylate having a polyoxyethylene structure and a unit based on (meth)acrylate having an alkoxysilyl group is exemplified.
• the present invention provides a copolymer and a composition capable of forming a surface layer with excellent non-adsorption properties, and an article with excellent non-adsorption properties.
• the present invention has the following aspects.
• Copolymer having a unit (A) having a reactive silyl group, a unit (B) having a group represented by the following formula (1), and a unit (C) having a group represented by the following formula (2) .
• n1 is 2 or 3
• n2 is an integer from 0 to 300.
• R 6 is an alkyl group
• n3 is 2 or 3
• n4 is an integer from 0 to 300
• the ratio expressed by the number of carbon atoms of (n4+1)/R 6 is 0.5 or more and less than 9. be.
• R is a hydrogen atom or a methyl group
• Q 3 is a single bond or a divalent organic group
• R 6 , n3 and n4 are the same as R 6 , n3 and n4 in the above formula (2), respectively.
• A The copolymer according to any one of [1] to [6] above, wherein the unit (A) is represented by the following formula (A-1).
• R is a hydrogen atom or a methyl group
• Q 2 is a divalent organic group
• R 7 is an alkyl group having 1 to 18 carbon atoms
• R 8 is a hydrogen atom or a C 1 to 18 alkyl group.
• t is an integer of 1 to 3
• each of the plurality of R 7 or R 8 may be the same or different.
• the unit (D) is represented by the following formula (D1) or (D2).
• n5 is an integer from 10 to 200
• X 1 and Y 1 are each independently a divalent group represented by the following formula (3) or (4)
• R 9 is a hydroxyl group, a methoxy group, or an ethoxy group.
• Q 7 is a divalent organic group
• Q 8 is a single bond or an alkylene group having 1 to 5 carbon atoms
• Q 9 is a cyano group or a methyl group
• Q 10 is represented by formula (3) or ( When the divalent group represented by 4) is X 1 , it is a single bond, and when the divalent group represented by formula (3) or (4) is Y 1 , it is an oxygen atom.
• the unit (D) is a unit represented by the formula (D1), The copolymer of [9] above, wherein X 1 and Y 1 in formula (D1) are each independently a divalent group represented by formula (3).
• a composition comprising the copolymer of any one of [1] to [10] above.
• the copolymer of the present invention can form a surface layer with excellent non-adsorption properties.
• the composition of the present invention can form a surface layer with excellent non-adsorption properties.
• the article of the present invention has excellent non-adsorption properties.
• (Meth)acrylate is a general term for acrylate and methacrylate.
• a unit based on a monomer means a portion derived from a monomer formed by polymerization of the monomer.
• the biocompatible group means a group that has the property of inhibiting biological components such as blood, cells, and proteins from adhering to the material surface and becoming immobile.
• a compound, group, structure, or unit represented by a chemical formula is also expressed as a compound, group, structure, or unit with the number of the formula.
• the compound represented by Formula 1 is also referred to as Compound 1
• the structure represented by Formula 1 is also referred to as Structure 1.
• " ⁇ " indicating a numerical range means that the numerical values written before and after it are included as lower and upper limits.
• a copolymer according to one embodiment of the present invention (hereinafter also referred to as “this copolymer”) has the following unit (A), the following unit (B), and the following unit (C). This polymer may further have the following unit (D) as required.
• the present polymer may further contain units other than the unit (A), the unit (B), the unit (C), and the unit (D), if necessary.
• Unit (A) has a reactive silyl group.
• the reactive silyl group is a general term for hydrolyzable silyl groups such as alkoxysilyl groups and silanol groups.
• the hydrolyzable silyl group undergoes a hydrolysis reaction to form a silanol group (Si-OH).
• Si-OH silanol group
• the silanol group generated by hydrolysis of the hydrolyzable silyl group is A dehydration condensation reaction occurs to form siloxane bonds (Si-O-Si), resulting in a cured product.
• the reactive silyl group is preferably an alkoxysilyl group, such as group (5).
• -Si(R 7 ) 3-t (OR 8 ) t Formula (5)
• R 7 is an alkyl group having 1 to 18 carbon atoms
• R 8 is a hydrogen atom or an alkyl group having 1 to 18 carbon atoms
• t is an integer of 1 to 3.
• each of the plurality of R 7 or R 8 may be the same or different. From a manufacturing standpoint, it is preferable that a plurality of R 7 or R 8 be the same.
• t is preferably 2 or more, and more preferably 3.
• R 7 is preferably an alkyl group having 1 to 6 carbon atoms, more preferably a methyl group or an ethyl group.
• R 8 is preferably an alkyl group having 1 to 6 carbon atoms, and more preferably a methyl group or an ethyl group.
• Examples of the unit (A) include the unit (A-1).
• R is a hydrogen atom or a methyl group
• Q 2 is a divalent organic group
• R 7 , R 8 and t are the same as R 7 , R 8 and t in the above formula (5), respectively. be.
• Q 2 is preferably a divalent hydrocarbon group having 2 to 10 carbon atoms.
• the divalent hydrocarbon group may have an etheric oxygen atom between carbon atoms, and a hydrogen atom may be substituted with a halogen atom or a hydroxyl group.
• halogen atoms include chlorine atoms and fluorine atoms.
• Q 2 is preferably -C 2 H 4 -, -C 3 H 6 -, or -C 4 H 8 -, more preferably -C 3 H 6 - or -C 4 H 8 -, and -C 3 H 6 - is particularly preferred.
• Unit (A) may be a unit based on (meth)acrylate (a-1).
• CH 2 CR-COO-Q 2 -Si(R 7 ) 3-t (OR 8 ) t
• Unit (B) has group (1).
• Group (1) functions as a biocompatible site.
• the presence of group (1) can prevent biological components such as cells and proteins from adhering to the surface and becoming immobile, and exhibits non-adsorption properties.
• n1 is 2 or 3
• n2 is an integer from 0 to 300.
• n2 is preferably 8 or less, more preferably 3 or less, and particularly preferably 0.
• Examples of the unit (B) include the unit (B-1).
• R is a hydrogen atom or a methyl group
• Q3 is a single bond or a divalent organic group
• n1 and n2 are the same as n1 and n2 in the formula (1), respectively.
• Examples of the divalent organic group in Q 3 include -O-Q 6 -.
• Q 6 is a divalent organic group.
• Q 3 is -O-Q 6 -
• the -O- side end of -O-Q 6 - is bonded to the carbonyl group adjacent to Q 3 .
• Examples of Q 6 include those similar to Q 2 in the above formula (A-1).
• Q3 is preferably a single bond.
• the unit (B-1) may be a unit based on (meth)acrylate (b-1).
• CH 2 CR-CO-Q 3 -O-(CH 2 ) n1 -(OCH 2 CH 2 ) n2 -OH
• Unit (C) has group (2).
• Group (2) like group (1), functions as a biocompatible site.
• R 6 is an alkyl group
• n3 is 2 or 3
• n4 is an integer from 0 to 300
• the ratio expressed by the number of carbon atoms of (n4+1)/R 6 is 0.5 or more. It is less than 9.
• R 6 may be linear or branched, preferably linear.
• the number of carbon atoms in R 6 is preferably 1 to 22, more preferably 1 to 5, particularly preferably 1 or 2, from the viewpoint of better non-adsorption properties.
• n4 may be any value such that the ratio expressed by the number of carbon atoms of (n4+1)/ R6 is 0.5 or more and less than 9, but from the viewpoint of better water resistance, it is preferably 0 to 100, and 0 to 39. is more preferable, and 0 to 7 is even more preferable. If the ratio expressed by the number of carbon atoms (n4+1)/R 6 is 0.5 or more, the non-adsorption property is excellent, and if it is less than 9, the non-adsorption property and water resistance are excellent.
• the ratio (n4+1)/R 6 expressed by the number of carbon atoms is preferably 8 or less, more preferably 6 or less.
• R 6 is preferably an alkyl group having 1 to 5 carbon atoms, and n4 is preferably 0 to 39. Among these, it is preferable that n3 is 3, n4 is 0, and R 6 is a methyl group, or n3 is 2, n4 is 0 to 7, and R 6 is a methyl group or an ethyl group. That is, as the group (2), -O-(CH 2 ) 3 -OCH 3 , -O-(CH 2 ) 2 -(O(CH 2 ) 2 ) n2 -OCH 3 , or -O-(CH 2 ) 2 -(O(CH 2 ) 2 ) n2 -OC 2 H 5 is preferred. When n3 is 2, n4 is preferably 6 or less, more preferably 5 or less, from the viewpoint of water resistance.
• Examples of the unit (C) include the unit (C-1).
• R is a hydrogen atom or a methyl group
• Q3 is a single bond or a divalent organic group
• n3, n4 and R6 are respectively n3, n4 and R6 in the above formula (2). It's the same.
• Examples of the divalent organic group for Q 3 in formula (C-1) include those similar to the divalent organic group for Q 3 in formula (B-1).
• unit (B) contains unit (B-1)
• unit (C) contains unit (C-1)
• R and Q3 in unit (C-1) are each unit (B-1). may be the same as or different from R and Q3 therein.
• the unit (C-1) may be a unit based on (meth)acrylate (c-1).
• CH 2 CR-CO-Q 3 -O-(CH 2 ) n3 -(OCH 2 CH 2 ) n4 -OR 6
• the unit (D) has a polyoxyethylene chain that constitutes the main chain of the present copolymer.
• the polyoxyethylene chain of the unit (D) functions as a biocompatible site similarly to the group (1) of the unit (B) and the group (2) of the unit (C).
• Examples of the unit (D) include the unit (D1) and the unit (D2).
• n5 is an integer of 10 to 200
• X 1 and Y 1 are each independently a divalent group (3) or (4)
• R 9 is a hydroxyl group, a methoxy group, or an ethoxy group.
• n5 is preferably 40 to 200, more preferably 40 to 140.
• Q 7 is a divalent organic group
• Q 8 is a single bond or an alkylene group having 1 to 5 carbon atoms
• Q 9 is a cyano group or a methyl group.
• Q10 is a single bond when the divalent group (3) or (4) is X1 , and is an oxygen atom when the divalent group (3) or (4) is Y1 .
• the terminal on the Q10 side is bonded to the oxygen atom adjacent to X1
• the divalent group (3) or (4) is Y1.
• the end on the Q 10 side is bonded to the carbon atom adjacent to Y 1 .
• Q 10 of the divalent group (3) or (4) is bonded to the oxygen atom side terminal and the carbon atom side terminal of the polyoxyethylene chain (OCH 2 CH 2 ) n5 , respectively.
• Q 10 of divalent group (3) or (4) is bonded to the oxygen atom side terminal of polyoxyethylene chain (OCH 2 CH 2 ) n5 .
• Q 7 is preferably a divalent hydrocarbon group having 2 to 10 carbon atoms.
• the divalent hydrocarbon group may have an etheric oxygen atom between carbon atoms, and a hydrogen atom may be substituted with a halogen atom, a hydroxyl group, or a cyano group.
• halogen atoms include chlorine atoms and fluorine atoms.
• Q 7 is preferably -C(CH 3 )(COOC 2 H 5 )-, -C(CH 3 )(COOCH 3 )- or -C(CH 3 )(CN)-, and -C(CH 3 )( COOCH 3 )- or -C(CH 3 )(CN)- is more preferred, and -C(CH 3 )(CN)- is particularly preferred.
• the alkylene group in Q 8 may be linear or branched, preferably linear.
• a unit (D1-1) in which X 1 and Y 1 are each independently a divalent group (3) is preferable because it is easily available.
• two Q 7 's in the unit (D1-1) may be the same or different.
• the polymerization initiator containing a polyoxyethylene chain and a radical generating site an azo polymerization initiator having a polyoxyethylene chain can be exemplified.
• a compound having the structure (PI) can be exemplified.
• Examples of the compound having the structure (PI) include VPE-0201 manufactured by Fuji Film Wako Pure Chemical Industries, Ltd.
• n5 is the same as n5 in formula (D1) or (D2), and n6 is an integer from 1 to 100.
• n6 is preferably 2 to 30, more preferably 3 to 20.
• Other units include, for example, units having biocompatible groups (excluding units (B), units (C), and units (D)), monomers having no biocompatible groups and reactive silyl groups.
• Examples include units based on Examples of units having a biocompatible group (excluding units (B), units (C), and units (D)) include those represented by formula (B2) or (B3) described in International Publication No. 2019/198374. The units used are listed below. Examples of the unit based on a monomer that does not have a biocompatible group and a reactive silyl group include a unit represented by formula (C) described in International Publication No. 2019/198374.
• the ratio of the unit (A) to all units constituting the present copolymer is preferably 0.1 to 50% by mass, more preferably 1.0 to 30% by mass, and even more preferably 3 to 25% by mass. If the proportion of the unit (A) is at least the above lower limit, the durability, water resistance and abrasion resistance will be better, and if it is below the above upper limit, the non-adsorption property will be better.
• the total ratio of units (B) and units (C) to all units constituting this copolymer is preferably 40 to 99.9% by mass, more preferably 50 to 99% by mass, and 60 to 97% by mass. More preferred. If the total ratio of units (B) and units (C) is equal to or higher than the lower limit value, the non-adsorption property is better, and if it is lower than the upper limit value, the non-adsorption durability, water resistance and abrasion resistance are improved. is better.
• the ratio of unit (B) to the total of unit (B) and unit (C) is preferably 0.1 to 90% by mass, more preferably 10 to 90% by mass, and even more preferably 30 to 90% by mass. If the proportion of the unit (B) is within the above range, the non-adsorption property and water resistance will be better.
• the ratio of the total of units (B) and units (C) to the total of units (B), units (C) and units (D) is preferably 50 mol% or more, more preferably 70 mol% or more, and 100 mol% It may be.
• the total ratio of units (A), units (B), units (C) and units (D) to all units constituting this copolymer is 50% by mass to all units constituting this copolymer.
• the content is preferably 75% by mass or more, more preferably 75% by mass or more, and may be 100% by mass.
• the mass average molecular weight (hereinafter also referred to as "Mw") of the present copolymer is preferably from 1,000 to 1,000,000, more preferably from 20,000 to 100,000, from the viewpoint of ease of production. Mw is calculated by size exclusion chromatography.
• This copolymer can be produced by a known method, for example, the method described in International Publication No. 2019/198374. For example, by polymerizing monomer components containing (meth)acrylate (a-1), (meth)acrylate (b-1), and (meth)acrylate (c-1) in the presence of a polymerization initiator. , a copolymer having units (A), units (B) and units (C) is obtained. At this time, a monomer containing a polyoxyethylene chain and a radically polymerizable group at both ends is included in the monomer component, or a polyoxyethylene chain and a radical generating site are used as a polymerization initiator. By using a polymerization initiator containing the following, a copolymer having units (A), units (B), units (C), and units (D) can be obtained.
• a surface layer with excellent non-adsorption properties can be formed.
• the non-adsorptive property tends to be inferior to when having only the unit (C).
• the non-adsorption property is improved compared to the case of only the unit (C), and furthermore, the water resistance is also improved.
• the switching between the hydrophobic part and the hydrophilic part is slow, and it is thought that the non-adsorption performance of the unit (C) is not fully expressed.
• the methyl group at the ⁇ position which is the hydrophobic part of the unit (B), has a low surface tension and is segregated at the air interface, and has a weak cohesive force. Therefore, it is thought that by coexisting unit (B) with unit (C), the cohesive force will be reduced without inhibiting the non-adsorption property, and the switch of unit (C) to the hydrophilic part will be faster when hydrated. It will be done.
• composition A composition according to one embodiment of the present invention (hereinafter also referred to as “the present composition”) contains the present copolymer.
• the present copolymer in the present composition may be one type or two or more types.
• the present composition may contain other components other than the present copolymer.
• other components include solid contents other than the present copolymer and liquid medium contained as solid contents in the cured product of the present composition.
• this composition is used to form a surface layer, which will be described later, and when the surface layer is formed by dry coating, the composition contains only solid content.
• the liquid medium that is removed during the formation of the surface layer is further included as other components.
• the other solid content may be a curable component like the present copolymer, or may be a non-curable component.
• Other solid contents include, for example, impurities that could not be removed from the raw materials and by-products used in the manufacturing process of this copolymer; catalysts and functional additives; groups (1) and (2); Compounds having one or both of these groups but not having a reactive silyl group; compounds having a biocompatible site other than group (1) and group (2); and compounds having a reactive silyl group can be mentioned.
• catalysts used for hydrolytic condensation reactions of reactive silyl groups can be used without particular limitation.
• specific examples of the catalyst include acids such as hydrochloric acid, nitric acid, acetic acid, sulfuric acid, phosphoric acid, and sulfonic acid, such as methanesulfonic acid and p-toluenesulfonic acid; bases such as sodium hydroxide, potassium hydroxide, and ammonia; and Examples include aluminum-based and titanium-based metal catalysts.
• functional additives include ultraviolet absorbers, light stabilizers, antioxidants, leveling agents, surfactants, antibacterial agents, dispersants, and inorganic fine particles.
• Examples of the compound having either one or both of group (1) and group (2) and having no reactive silyl group include (meth)acrylate alone having group (1) or group (2). Examples include polymers.
• the liquid medium can be appropriately selected from various known liquid media.
• the liquid medium is preferably capable of uniformly dissolving or dispersing the solid content containing the present copolymer.
• the boiling point of the liquid medium is preferably 60 to 160°C, more preferably 60 to 120°C, since the liquid medium must ultimately be removed when forming a cured product.
• liquid medium examples include isopropyl alcohol, ethanol, propylene glycol monomethyl ether, 2-butanone, and ethyl acetate. These may be used alone or in combination of two or more.
• the liquid medium can contain water for the hydrolysis reaction of the reactive silyl group-containing component such as the present copolymer, but preferably does not contain water from the viewpoint of storage stability. Even when the liquid medium does not contain water, the reactive silyl group-containing component can be hydrolyzed by atmospheric moisture.
• the content of the present copolymer in the present composition is preferably 30% by mass or more, and 50% by mass or more based on the total solid content, from the viewpoint of non-adsorption property, non-adsorption durability, water resistance and abrasion resistance. % or more, more preferably 70% by mass or more, and may be 100% by mass.
• the content of the catalyst is preferably 0.01 to 20% by mass, more preferably 0.1 to 5% by mass, based on the content of the present copolymer.
• the solid content concentration of the present composition is preferably 0.01 to 50% by mass, more preferably 0.1 to 30% by mass, based on the total mass of the composition.
• the thickness of the surface layer formed by wet coating using the present composition tends to be within a suitable range that can sufficiently exhibit non-adsorption properties and durability.
• the solid content concentration of the composition can be calculated from the mass of the composition after vacuum drying at 80° C. for 3 hours and the mass of the composition before heating.
• the solid content concentration of the present composition may be calculated from the total solid content and the amount of liquid medium added at the time of manufacturing the present composition.
• the content of the liquid medium is preferably 50 to 99.99% by mass, more preferably 70 to 99.9% by mass, based on the total mass of the composition.
• the method for producing the present composition is not particularly limited.
• the solid content containing the present copolymer further contains a liquid medium
• these solid content and the liquid medium may be mixed.
• the present copolymer in the present composition may be partially hydrolyzed and cocondensed to form a partially hydrolyzed cocondensate.
• the present copolymer and a reactive silane compound having no biocompatible site may be partially hydrolyzed and cocondensed to form a partially hydrolyzed cocondensate.
• the degree of condensation is appropriately adjusted so that the viscosity is such that it does not interfere with the formation of a surface layer on the base material as described below.
• the Mw of the partial hydrolysis condensate is preferably 2,000 to 2,000,000, more preferably 30,000 to 300,000.
• An article according to an embodiment of the present invention (hereinafter also referred to as “the article”) includes a base material and a surface layer disposed on the base material.
• the surface layer consists of a cured product of the present composition.
• the surface layer consisting of a cured product of the present composition means that the surface layer contains at least a cured product of a reactive silyl group-containing component containing the present copolymer.
• the material constituting the base material there are no particular restrictions on the material constituting the base material.
• Specific examples of the constituent material of the base material include metal, resin, glass, and composite materials of two or more of these, and are appropriately selected depending on the purpose.
• the constituent material of the base material is preferably a material having a hydroxyl group on the surface of a molded product made of the material, and glass is preferable.
• a conventionally known method for example, a physical treatment method such as corona treatment or a chemical treatment method such as limer treatment.
• the base material does not need to be entirely made of the above material, as long as at least part or all of the surface on which the surface layer is provided is made of the above material.
• a method using a compound containing an alkoxysilyl group such as tetraethoxysilane or a partially hydrolyzed condensate thereof, or a method using a metal oxide such as silica is preferable.
• the primer treatment method either wet coating or dry coating may be used.
• the thickness of the surface layer is preferably 10 to 100,000 nm, particularly preferably 10 to 10,000 nm. If the thickness of the surface layer is at least the above lower limit, sufficient non-adsorption properties, durability and water resistance are likely to be exhibited. If the thickness of the surface layer is below the upper limit, the strength will be better.
• the thickness of the surface layer is determined by measurement using an X-ray reflectance measuring device typified by Rigaku's ATX-G.
• This article is obtained by forming a surface layer on the surface of a base material using the present composition.
• methods for forming the surface layer include dry coating such as vacuum evaporation, CVD, and sputtering, and wet coating, with wet coating being preferred.
• a method for forming a surface layer by wet coating includes applying the composition containing the above-described liquid medium onto a substrate to obtain a coating film (hereinafter also referred to as “coating process”); Examples include a method that includes curing the coating film to obtain a surface layer (hereinafter also referred to as “curing step”).
• Examples of methods for applying the present composition in the coating step include dip coating, spin coating, wipe coating, spray coating, squeegee coating, die coating, inkjet coating, flow coating, roll coating, and casting.
• Examples include the Langmuir-Blodgett method and the gravure coating method.
• Heating is preferred as a method for curing the coating film in the curing step.
• the heating temperature depends on the type of the reactive silyl group-containing component containing the present copolymer, but is preferably 50 to 150°C, more preferably 100 to 150°C. Note that during the curing process, the liquid medium is usually removed at the same time. Therefore, the heating temperature is preferably higher than the boiling point of the liquid medium. However, if drying by heating is difficult due to the material of the base material, etc., heating is avoided and the liquid medium is removed. Examples of this method include drying under reduced pressure.
• the present composition does not contain water
• treatment such as humidification may be performed simultaneously with the curing step, or before or after the curing step.
• the excess compound in the surface layer may be removed as necessary.
• Specific methods include, for example, spraying the surface layer with a solvent, such as the compound used as the liquid medium of the present composition, or using a cloth impregnated with a solvent, such as the compound used as the liquid medium of the present composition. One method is to wipe it off.
• this composition can also be used as a repair agent for deterioration of the surface layer.
• the coating method is preferably wet coating such as spray coating or brush coating.
• the curing method is preferably heating using a dryer or the like.
• this product is not particularly limited, but since it has excellent non-adsorption properties, non-adsorption durability, water resistance, and scratch resistance, it has a surface that comes into contact with biological components such as blood and proteins.
• Specific articles include, for example, endoscopes, catheters, medical treatment instruments, artificial blood vessels, artificial joints, bags, heart-lung machines, tubes, stents, tips, ampoules, vials, syringes, needles, and for 3D printing of proteins.
• medical devices such as instruments; bioanalytical equipment components such as needles, chips, and vials; and physical and chemical instruments such as petri dishes, plates, vials, and chips. Among these, medical devices are preferred because they have many opportunities for contact with biological components.
• the amount of protein (mg/mL) in a 0.1 N NaOH aqueous solution containing 5 wt% sodium dodecyl sulfate (SDS) and the micro BCA reagent was determined using a calibration curve created by absorbance measurement using a protein solution with a known concentration. The smaller the amount of protein, the better the non-adsorption property.
• the silicon wafer with the film was washed with pure water to wash away impurities including low molecular components on the film surface.
• the film thickness of the film was measured using Filmetrics F20-UV, and this was taken as the initial film thickness.
• the silicon wafer with the membrane was immersed in 200 mL of physiological saline (D-PBS(-)) for 30 days. After 30 days, the silicon wafer with the film was taken out and dried on a hot plate at 40° C. for 30 minutes.
• VPE0201 Azo polymerization initiator having a polyoxyethylene chain (a compound having a structure in which n5 is 45 to 46 and n6 is 6 to 14 in the above formula (PI), molecular weight 2240, manufactured by Fujifilm Wako Pure Chemical Industries, Ltd. "VPE” -0201”).
• Example 1-6 and 9-21 Each component was dissolved in a mixed solvent of methoxypropanol and diacetone alcohol at a ratio of 85:15 (mass ratio) at the ratio (wt%) shown in Table 1 so that the solid content concentration was 20 wt%.
• the obtained solution was placed in a pressure-resistant glass bottle, sealed, and then heated at 80° C. for 24 hours to perform polymerization to obtain a copolymer solution with a solid content concentration of 20 wt%.
• Example 7-8 A copolymer solution with a solid content concentration of 20 wt% was obtained in the same manner as in Examples 1 to 6 and 9 to 21, except that azobisisobutyronitrile was used instead of VPE0201 as a polymerization initiator. The obtained copolymer solution was evaluated as described above. The results are shown in Table 1.
• Table 1 shows the ratio (wt%) of unit (B) to the total of unit (B) and unit (C), and the unit (B) and unit to the total of unit (B), unit (C), and unit (D). The total percentage (mol%) of (C) is also listed.
• Examples 1 to 8 and 15 to 21 had excellent non-adsorption properties and water resistance.
• Examples 9 to 11 containing a unit based on PEG9A instead of the unit (C) had inferior non-adsorption properties compared to Examples 1 to 8 and 15 to 21.
• Examples 9 and 10 which had a relatively large proportion of units based on PEG9A, also had poor water resistance.
• Example 12 which did not contain the unit (C), had the poorest non-adsorption properties.
• Examples 13 to 14, which did not contain the unit (B) had poorer non-adsorption properties and poorer water resistance than Examples 1 to 8 and 15 to 21.

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