JP2005126635A - Coating composition for can - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a coating composition for a can excellent in curability, processability and adhesiveness, having excellent retort resistance, and substantially free from bisphenol A. <P>SOLUTION: This coating composition for the can comprises a polyester resin (A) having an aromatic ring with a phenolic hydroxy group in which at least one site of an ortho-position and a para-position to the hydroxy group is a hydrogen atom, a linear saturated copolyester resin (B) and a phenol resin (C). <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to a coating composition for cans that uses a specific polyester resin in combination, has excellent food hygiene, has retort resistance, and does not substantially contain bisphenol A.

  Conventionally, metals such as aluminum, tin, and tin-free steel are used as the metal can material. In order to prevent corrosion of these metals, a coating film is usually formed on the inner and outer surfaces of the can. As can coatings, epoxy / phenol resin-based and epoxy / amino resin-based coatings are usually used because they are excellent in adhesion and corrosion resistance.

  However, in recent years, a coating system that does not contain bisphenol A has been demanded due to the problem of elution amount of bisphenol A, which is suspected as an environmental hormone. As such a paint for cans, a polyester-acrylic thermosetting paint (for example, see Patent Document 1) and a paint containing a polyester resin and a phenol resin (for example, see Patent Document 2) have been proposed. Furthermore, a paint using a polyester resin having a phenolic hydroxyl group introduced together with a curing agent (see, for example, Patent Document 3) has also been proposed.

  However, these conventional coating systems that do not contain bisphenol A exhibit good performance for individual items when used for cans, but they are well balanced in curability, workability, retort resistance, and adhesion. Not. Therefore, there is a need for a paint for cans that provides a coating film that is well-balanced with respect to these physical properties.

JP 2000-290585 A JP 2001-131470 A JP 2002-088231 A

  The subject of this invention is providing the coating composition for cans which does not contain bisphenol A substantially, is excellent in sclerosis | hardenability, workability, and adhesiveness, and has the outstanding retort resistance.

  As a result of intensive studies, the present inventors have found an excellent can coating composition by using a specific polyester resin together with a phenol resin, and have completed the present invention.

  That is, the present invention relates to a polyester resin (A) having an aromatic ring having a phenolic hydroxyl group and having at least one ortho-position and para-position relative to the hydroxyl group, and a linear shape having no phenolic hydroxyl group. A can coating composition comprising a saturated copolymerized polyester resin (B) and a phenol resin (C) is provided.

  The can coating composition of the present invention is excellent in the balance of coating film properties such as curability, processability, adhesion, and retort resistance by using a specific polyester resin in combination with a phenol resin. Furthermore, the can coating composition of the present invention does not substantially contain bisphenol A, and is extremely excellent as a composition used for food containers, particularly for can inner coatings.

  The constitution of the present invention comprises a polyester resin (A) having a phenolic hydroxyl group and having an aromatic ring in which at least one of the ortho-position and para-position with respect to the hydroxyl group is a hydrogen atom, linear having no phenolic hydroxyl group A can coating composition comprising a saturated copolymerized polyester resin (B) and a phenol resin (C).

  Hereinafter, each component will be described in detail. The polyester resin (A) used in the can coating composition of the present invention has a phenolic hydroxyl group and a polyester resin having an aromatic ring in which at least one of the ortho and para positions is a hydrogen atom with respect to the hydroxyl group ( A). As a raw material for introducing a phenolic hydroxyl group into a polyester resin, it has a hydroxyl group and / or a carboxyl group for forming an ester bond, and at least one of the phenolic hydroxyl group and the ortho position and para position with respect to the hydroxyl group is hydrogen. Examples thereof include compounds having an aromatic ring as an atom. Preferably, it is diphenolic acid.

  The amount of diphenolic acid introduced in the polyester resin (A) is preferably in the range of 2 to 10% by mass in terms of maintaining curability and retort resistance performance.

  The dibasic acid component constituting the polyester resin (A) having a phenolic hydroxyl group includes succinic acid, adipic acid, azelaic acid, sebacic acid, maleic acid, fumaric acid, phthalic anhydride, phthalic acid, isophthalic acid, terephthalic acid Examples include acid, trimellitic acid, trimellitic anhydride, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, itaconic acid, pyromellitic anhydride, and succinic anhydride.

  As a glycol component (polyhydric alcohol component) constituting the polyester resin (A) having a phenolic hydroxyl group, ethylene glycol, propylene glycol, 1,3-butanediol, 2,3-butanediol, 1,4-butane Examples thereof include diol, 2-methyl-1,3-propanediol, neopentyl glycol, diethylene glycol, dipropylene glycol, glycerin, trimethylol ethane, trimethylol propane, cyclohexane dimethanol, and pentaerythritol.

  It is preferable that the glass transition temperature (Tg) of the polyester resin (A) having the phenolic hydroxyl group described above is 20 to 60 ° C. in terms of maintaining workability, adhesion, and retort resistance. More preferably, it is 30-50 degreeC.

  The number average molecular weight of the polyester resin (A) having a phenolic hydroxyl group is preferably 3000 to 20000. By being in this range, processability, curability, and adhesion are improved. More preferably, the number average molecular weight is 5,000 to 18,000, and particularly preferably 6,000 to 12,000.

  The number average molecular weight is measured by gel permeation chromatography (GPC) and determined in terms of polystyrene.

  Examples of the method for introducing diphenolic acid into the polyester resin include known methods described in JP-A-2002-88231.

  The dibasic acid component constituting the linear saturated copolyester resin (B) includes succinic acid, adipic acid, azelaic acid, sebacic acid, maleic acid, fumaric acid, phthalic anhydride, phthalic acid, isophthalic acid, terephthalic acid Examples include acid, trimellitic acid, trimellitic anhydride, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, itaconic acid, pyromellitic anhydride, and succinic anhydride.

  The glycol component constituting the linear saturated copolymerized polyester resin (B) includes ethylene glycol, propylene glycol, 1,3-butanediol, 2,3-butanediol, 1,4-butanediol, 2-methyl- Examples thereof include 1,3-propanediol, neopentyl glycol, diethylene glycol, dipropylene glycol, glycerin, trimethylol ethane, trimethylol propane, cyclohexane dimethanol, pentaerythritol and the like.

  It is preferable that the glass transition temperature (Tg) of the linear saturated copolymerized polyester resin (B) is 20 to 60 ° C. in terms of maintaining workability, adhesion, and retort resistance. More preferably, it is 30-50 degreeC.

  The number average molecular weight of the linear saturated copolyester resin (B) is preferably 3000 to 20000. By being in this range, workability and adhesion are improved. More preferably, the number average molecular weight is 5000 to 18000, and particularly preferably 6000 to 16000.

  The coating composition for cans of the present invention is a content ratio of the polyester resin (A) having a phenolic hydroxyl group to the total amount of the polyester resin (A) having a phenolic hydroxyl group and the linear saturated copolymerized polyester resin (B). However, it is preferable to contain in the ratio of (A) / (A) + (B) = 5 / 100-95 / 100 by solid content mass ratio. When the content ratio of the polyester resin (A) having a phenolic hydroxyl group is smaller than the above ratio, sufficient curability and retort resistance may not be obtained, and when the ratio is larger than the above ratio, it is sufficient. Workability and adhesion may not be obtained. More preferably, it is 10/100 to 50/100, and particularly preferably 20/100 to 30/100.

  The phenol resin (C) used in the can coating composition of the present invention is preferably a resol type phenol resin not containing bisphenol A. To exemplify only typical ones as the phenol resin (C), various tetrafunctional phenol compounds containing no bisphenol A, carboxylic acid, m-ethylphenol, 3,5-xylenol, m-methoxy Trifunctional phenolic compounds such as phenol or various bifunctional phenols such as p-cresol, o-cresol, p-tert-butylphenol, p-ethylphenol, 2,3-xylenol, m-methoxyphenol, A product obtained by reacting formaldehyde with an alkali catalyst.

  Moreover, the thing of the form which etherified one part or all part of the methylol group contained in a phenol resin by alcohol with 1-12 carbon atoms can also be used.

  The coating composition for cans of the present invention contains the phenol resin (C) with respect to the total amount of the polyester resin (A) having a phenolic hydroxyl group, the linear saturated copolymerized polyester resin (B), and the phenol resin (C). It is preferable that it is a coating composition for cans in which the ratio is (C) / (A) + (B) + (C) = 5/100 to 50/100 in terms of solid content mass ratio. When the content ratio of the phenol resin (C) is smaller than the above, sufficient curability and retort resistance may not be obtained. When the content ratio is larger than the above ratio, sufficient workability and work adhesion are obtained. It may not be obtained. Preferably, it is 10 / 100-40 / 100, More preferably, it is 20 / 100-30 / 100.

  As the solvent used in the can coating composition of the present invention, any solvent known per se can be used as long as it can dissolve the resin component described above. Although the following can be used suitably, of course, it is not limited to this example. Toluene, xylene, cyclohexanone, isopropyl alcohol (IPA), normal butanol, ethylene glycol monomethyl ether (methyl cellosolve), ethylene glycol monoethyl ether (cellosolve), ethylene glycol monobutyl ether (butyl cellosolve), Solvesso 100, Solvesso 150, Solfit ( 3-methyl-3-methoxybutanol), propylene glycol monomethyl ether, methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK), isophorone, ethyl glycol acetate, ethyl acetate, isopropyl acetate, butyl acetate, PGMAC (propylene glycol monomethyl ether acetate) Solfit AC (3-methyl-3methoxybutyl acetate), EDG C (carbitol acetate), in a solvent such as DBE (dibasic esters), these may be used alone or in combination thereof used.

  In the can coating composition of the present invention, various additives conventionally used in this type of coating can be blended based on a formulation known per se. Although the following can be used suitably, of course, it is not limited to this example. Pigments such as titanium oxide, zinc oxide and aluminum, lubricants such as petroleum wax, silicon and fatty acid amides, additives such as acrylic polymers, antifoaming agents such as silicon, and leveling agents. You may use the above together.

  Moreover, the coating composition for cans of this invention can mix | blend a curing catalyst based on formulation known per se at the time of a hardening process. If only typical ones are exemplified as curing catalysts, it is possible to use inorganic acids such as phosphoric acid, organic acids such as dodecylbenzenesulfonic acid and toluenesulfonic acid, and those blocked with an amine or the like. it can.

  The can coating composition of the present invention can be produced by mixing and stirring the above-described components. The content ratio of each component of the can coating composition is preferably in the above-described range.

  The can coating composition of the present invention can be applied to a metal plate known per se. The coating composition for cans of the present invention can form a coating film suitable for can coating by coating and baking on a metal plate or the inner surface of a processed can.

  As the metal plate used for the above can, any metal plate can be used as long as it can be used for beverage cans, cans for cans, lids, caps, such as aluminum plates, tin-free steel plates, tin plates, etc. Can be mentioned.

The can coating composition of the present invention can be applied by a known coating method such as roll coater coating or spray coating, and the coating amount is not particularly limited, but the dry coating amount is 30 mg / dm. it is preferably in the range of ^{2 ~200mg} / dm ^2, and more preferably in the range of ^{60mg / dm 2 ~150mg / dm 2} .

  The baking condition is preferably 90 to 280 ° C. and 10 seconds to 30 minutes.

  It can be used for food cans, beverage cans, art cans, lids, etc. for metal plate coating, but the most preferred application is to use for inner coating of various metal containers used for food and drink, etc. The coating film is water resistant, there is no elution of low molecular weight compounds from the coating film into the can contents, and in addition, the coating film is extremely impervious, so the natural nature of food and drink stored inside the can A coated product that does not alter the taste or scent of the product and is excellent in processability can be obtained.

  The present invention will be described more specifically with reference to examples. In the following, unless otherwise specified, all parts and% are based on mass.

(Production Example 1)
It consists of isophthalic acid, terephthalic acid, sebacic acid, diphenolic acid as the acid component, and ethylene glycol, 1,4-butanediol, 2-methyl-1,3-propanediol, and cyclohexanedimethanol as the glycol component, and has a number average molecular weight. A polyester resin having a phenolic hydroxyl group of 7000, Tg of 45 ° C., a hydroxyl value of 30 mgKOH / g to 32 mgKOH / g, and an acid value of 1 mgKOH / g or less was obtained. This resin was diluted with a mixed solvent to obtain a polyester resin (A-1) having a phenolic hydroxyl group having a resin solid content of 40%.

(Production Example 2)
It consists of isophthalic acid, terephthalic acid, sebacic acid, diphenolic acid as the acid component, and ethylene glycol, 1,4-butanediol, 2-methyl-1,3-propanediol, and cyclohexanedimethanol as the glycol component, and has a number average molecular weight. A polyester resin having a phenolic hydroxyl group of 7000, Tg of 65 ° C., a hydroxyl value of 30 mgKOH / g to 32 mgKOH / g, and an acid value of 1 mgKOH / g or less was obtained. This resin was diluted with a mixed solvent to obtain a polyester resin (A-2) having a phenolic hydroxyl group having a resin solid content of 40%.

(Production Example 3)
It consists of isophthalic acid, terephthalic acid, sebacic acid, diphenolic acid as the acid component, and ethylene glycol, 1,4-butanediol, 2-methyl-1,3-propanediol, and cyclohexanedimethanol as the glycol component, and has a number average molecular weight. A polyester resin having a phenolic hydroxyl group having 2000, Tg of 45 ° C., a hydroxyl value of 30 mgKOH / g to 32 mgKOH / g, and an acid value of 1 mgKOH / g or less was obtained. This resin was diluted with a mixed solvent to obtain a polyester resin (A-3) having a phenolic hydroxyl group with a resin solid content of 40%.

(Production Example 4)
The acid component is isophthalic acid, terephthalic acid, sebacic acid, and the glycol component is ethylene glycol, 1,4-butanediol, 2-methyl-1,3-propanediol, cyclohexanedimethanol, number average molecular weight 15000, Tg 40 ° C. Thus, a linear saturated copolymer polyester resin having a hydroxyl value of 8 to 10 mgKOH / g and an acid value of 1 mgKOH / g or less was obtained. This resin was diluted with a mixed solvent to obtain a linear saturated copolymer polyester resin (B-1) having a resin solid content of 40%.

(Production Example 5)
The acid component is isophthalic acid, terephthalic acid, sebacic acid, and the glycol component is ethylene glycol, 1,4-butanediol, 2-methyl-1,3-propanediol, cyclohexanedimethanol, number average molecular weight 15000, Tg 68 ° C. Thus, a linear saturated copolymer polyester resin having a hydroxyl value of 8 to 10 mgKOH / g and an acid value of 1 mgKOH / g or less was obtained. This resin was diluted with a mixed solvent to obtain a linear saturated copolymer polyester resin (B-2) having a resin solid content of 40%.

(Production Example 6)
The acid component is isophthalic acid, terephthalic acid, sebacic acid, and the glycol component is ethylene glycol, 1,4-butanediol, 2-methyl-1,3-propanediol, cyclohexanedimethanol, number average molecular weight 2000, Tg 40 ° C. Thus, a linear saturated copolymer polyester resin having a hydroxyl value of 8 to 10 mgKOH / g and an acid value of 1 mgKOH / g or less was obtained. This resin was diluted with a mixed solvent to obtain a linear saturated copolymer polyester resin (B-3) having a resin solid content of 40%.

(Production Example 7)
After a xylenol component and formaldehyde were heated and subjected to a condensation reaction under alkaline conditions, a methylol group was partially etherified to obtain a xylenol-resole type resin. This resin was diluted with a mixed solvent to obtain a phenol resin (C-1) having a resin solid content of 70%.

(Example 1 Preparation of paint)
170 parts of polyester resin (A-1) having phenolic hydroxyl group of Production Example 1, 510 parts of linear saturated copolymerized polyester resin (B-1) of Production Example 4, and phenol resin (C-1) 97 of Production Example 7 Part 1, 223 parts of a mixed solvent consisting of cyclohexanone, xylene and others was mixed to prepare Example 1 paint having a solid content of 34%.

(Example 2 Preparation of paint)
Polyester resin (A-1) 340 parts having a phenolic hydroxyl group, linear saturated copolymerized polyester resin (B-1) 340 parts, phenol resin (C-1) 97 parts, mixed solvent 223 comprising cyclohexanone, xylene and others Part 2 was mixed to prepare Example 2 paint having a solid content of 34%.

(Example 3 Preparation of paint)
A mixed solvent 332 comprising 106 parts of a polyester resin (A-1) having a phenolic hydroxyl group, 319 parts of a linear saturated copolyester resin (B-1), 243 parts of a phenol resin (C-1), cyclohexanone, xylene and others. Part 3 were mixed to prepare Example 3 paint having a solid content of 34%.

(Example 4 Preparation of paint)
A mixed solvent 440 comprising 43 parts of a polyester resin (A-1) having a phenolic hydroxyl group, 128 parts of a linear saturated copolymerized polyester resin (B-1), 389 parts of a phenol resin (C-1), cyclohexanone, xylene and others. Parts 4 were mixed to prepare Example 4 paint having a solid content of 34%.

(Example 5 Preparation of paint)
170 parts of a polyester resin (A-2) having a phenolic hydroxyl group, 510 parts of a linear saturated polyester resin (B-1), 97 parts of a phenol resin (C-1), 223 parts of a mixed solvent comprising cyclohexanone, xylene and others Example 5 paint having a solid content of 34% was prepared by mixing.

(Example 6 Preparation of paint)
170 parts of a polyester resin (A-3) having a phenolic hydroxyl group, 510 parts of a linear saturated polyester resin (B-1), 97 parts of a phenol resin (C-1), 223 parts of a mixed solvent consisting of cyclohexanone, xylene, etc. Example 6 paint with a solid content of 34% was prepared by mixing.

(Example 7 Preparation of paint)
170 parts of polyester resin (A-1) having a phenolic hydroxyl group, 510 parts of linear saturated copolymerized polyester resin (B-2), 97 parts of phenolic resin (C-1), mixed solvent 223 comprising cyclohexanone, xylene and others Parts were mixed to prepare Example 7 paint having a solid content of 34%.

(Example 8 Preparation of paint)
170 parts of polyester resin (A-1) having a phenolic hydroxyl group, 510 parts of linear saturated copolyester resin (B-3), 97 parts of phenol resin (C-1), cyclohexanone, xylene, etc. 223 parts of mixed solvent was mixed to prepare Example 8 paint having a solid content of 34%.

(Comparative Example 1 Preparation of paint)
Comparative Example 1 having a solid content of 34% was prepared by mixing 680 parts of linear saturated copolyester resin (B-1), 97 parts of phenolic resin (C-1), and 223 parts of a mixed solvent consisting of cyclohexanone, xylene and others. A paint was prepared.

(Comparative Example 2 Preparation of paint)
Comparative Example 2 in which 680 parts of polyester resin (A-1) having a phenolic hydroxyl group, 97 parts of phenol resin (C-1), and 223 parts of a mixed solvent consisting of cyclohexanone, xylene and others are mixed and the solid content is 34%. A paint was prepared.

(Comparative Example 3 Preparation of paint)
213 parts of a polyester resin (A-1) having a phenolic hydroxyl group, 638 parts of a linear saturated copolymerized polyester resin (B-1), 150 parts of a mixed solvent composed of cyclohexanone, xylene and others are mixed to obtain a solid content of 34. % Comparative Example 3 paint was prepared.

The test method for can coating compositions is described below. The above-described example paint and comparative paint were applied to an aluminum plate with a bar coater so that the dry coating amount was 60 mg / dm ² and baked at 205 ° C. for 10 minutes, and various models were evaluated. It was. As model evaluation, curability, retort resistance, workability, and adhesion were evaluated.

(Curable)
The extraction rate (%) after 1 hour of boiling MEK (methyl ethyl ketone) was measured on a coated plate that had been subjected to a retort treatment at 120 ° C. for 90 minutes in tap water, and evaluated by the following method.
A: The extraction amount is less than 10%.
○: The extraction rate is 10% or more and less than 20%.
□: Extraction rate is 20% or more and less than 30%.
Δ: Extraction rate is 30% or more and less than 40%.
X: Extraction amount is 40% or more.

(Processability)
Bending tip of the sample after folding the tin plate between two test pieces with the coating film outside and folding the plate between the two, and then performing retort treatment at 120 ° C for 90 minutes in tap water Then, a current value (mA) of a processed part 2 cm width when a voltage of 6 V was applied for 3 seconds was measured and evaluated by the following method.
A: The energization amount is less than 10 mA.
○: The energization amount is 10 mA or more and less than 20 mA.
□: The energization amount is 20 mA or more and less than 30 mA.
Δ: The energization amount is 30 mA or more and less than 40 mA.
X: The energization amount is 40 mA or more.

(Retort resistance of coating film)
The painted plate was visually evaluated by whitening and swelling when it was subjected to a retort treatment at 120 ° C. for 90 minutes in tap water.
○: No abnormality □: Slight whitening and swelling ×: Significant whitening and swelling

(Adhesion)
On the formed coating film, 100 grids of 1 mm × 1 mm were prepared with a cutter, and this sample piece was retorted at 120 ° C. for 90 minutes in tap water. The cellophane pressure-sensitive adhesive tape was then applied to the grid area, and then the cellophane pressure-sensitive adhesive tape was peeled off rapidly, and the peeled state of the coating film was observed.
A: No peeling at all O: 1% or more and less than 5% of the whole peeled off.
□: 5% or more and less than 15% of the whole peeled off.
Δ: 15% or more and less than 20% of the whole peeled off.
X: 20% or more of the whole peeled off.

  Tables 1 and 2 summarize the formulation compositions and evaluation results of Examples 1 to 8 and Comparative Examples 1 to 3.

  The comparative example 1 which does not contain the polyester resin (A) component which has a phenolic hydroxyl group satisfy | fills workability and adhesiveness, However, Curability and retort resistance are inadequate, A linear saturated copolymerization polyester resin (B) Comparative Example 2 containing no component is excellent in curability but has insufficient workability and adhesion. Moreover, the comparative example 3 which does not contain a phenol resin (C) component lacks especially retort resistance. On the other hand, the can coating composition of the present invention having a polyester resin (A) having a phenolic hydroxyl group, a linear saturated copolymerized polyester resin (B) and a phenol resin (C) is curable, workable, The physical properties of adhesion and retort resistance were balanced, and good results were shown.

  By making the molecular weights of the polyester resin (A) having a phenolic hydroxyl group and the linear saturated copolymerized polyester resin (B) each in the range of 3000 to 20000, the processability and adhesion are particularly excellent. Moreover, the coating composition for cans which is excellent in workability and adhesiveness even when the Tg of the polyester resin (A) having a phenolic hydroxyl group and the linear saturated copolymerized polyester resin (B) is in the range of 20 to 60 ° C., respectively. Is obtained.

In addition to the well-balanced physical properties required for can coatings, such as curability, processability, retort resistance, and adhesion, it is effective as a paint for cans, especially as a paint composition for can inner surfaces, as a composition not containing bisphenol A. Can be used.

Claims (7)

Polyester resin (A) having a phenolic hydroxyl group and having an aromatic ring in which at least one of ortho-position and para-position with respect to the hydroxyl group is a hydrogen atom, linear saturated copolyester resin having no phenolic hydroxyl group ( A can coating composition comprising B) and a phenol resin (C). The can coating composition according to claim 1, wherein the polyester resin (A) having a phenolic hydroxyl group is a diphenol acid-modified polyester resin. The number average molecular weight of the polyester resin (A) having the phenolic hydroxyl group described above is 3000 to 20000, and the number average molecular weight of the linear saturated copolymerized polyester resin (B) is 3000 to 20000. The coating composition for cans according to 1. The glass transition temperature (Tg) of the polyester resin (A) having the phenolic hydroxyl group described above is 20 to 60 ° C., and the glass transition temperature (Tg) of the linear saturated copolymerized polyester resin (B) is 20 to 60 ° C. The coating composition for cans according to any one of claims 1 to 3, which is at ° C. The can coating composition according to any one of claims 1 to 4, wherein the phenol resin (C) is a resol type phenol resin not containing bisphenol A. The content ratio of the polyester resin (A) having a phenolic hydroxyl group to the total amount of the polyester resin (A) having a phenolic hydroxyl group and the linear saturated copolymerized polyester resin (B) is represented by a solid content mass ratio. ) / (A) + (B) = 5/100 to 95/100 The coating composition for cans according to any one of claims 1 to 5. The content ratio of the phenol resin (C) to the total amount of the above-described polyester resin (A) having a phenolic hydroxyl group, linear saturated copolymer polyester resin (B), and phenol resin (C) is a solid content mass ratio. C) / (A) + (B) + (C) = 5 / 100-50 / 100 The coating composition for cans according to any one of claims 1 to 6.