Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JP4058855B2 - Printing ink composition for laminate cans - Google Patents
[go: Go Back, main page]

JP4058855B2 - Printing ink composition for laminate cans - Google Patents

Printing ink composition for laminate cans Download PDF

Info

Publication number
JP4058855B2
JP4058855B2 JP27422799A JP27422799A JP4058855B2 JP 4058855 B2 JP4058855 B2 JP 4058855B2 JP 27422799 A JP27422799 A JP 27422799A JP 27422799 A JP27422799 A JP 27422799A JP 4058855 B2 JP4058855 B2 JP 4058855B2
Authority
JP
Japan
Prior art keywords
printing ink
ink composition
isocyanate compound
resin
parts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP27422799A
Other languages
Japanese (ja)
Other versions
JP2001098192A (en
Inventor
輝 長井
守弘 岡田
隆雄 戸島
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DIC Corp
Original Assignee
Dainippon Ink and Chemicals Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dainippon Ink and Chemicals Co Ltd filed Critical Dainippon Ink and Chemicals Co Ltd
Priority to JP27422799A priority Critical patent/JP4058855B2/en
Publication of JP2001098192A publication Critical patent/JP2001098192A/en
Application granted granted Critical
Publication of JP4058855B2 publication Critical patent/JP4058855B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Paints Or Removers (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Description

【0001】
【発明の属する技術分野】
本発明は、清涼飲料,コーヒー,紅茶,お茶,ビール等の飲料缶、缶詰、エアゾール缶、美術缶の如く金属缶材の耐熱、美粧、耐蝕、防錆用として使用されるラミネート金属板に使用される印刷インキ組成物に関する。
【0002】
【従来の技術】
高生産性、優れたフレーバー性、環境ホルモン対策、鮮明な印刷効果等の利点よりポリエステルフィルムにグラビア印刷を施し、それを接着剤にて金属板に貼り合わせるラミネート金属板方式が数年前より実用化されている。接着剤としては、エポキシ、ポリエステル、ポリウレタン系樹脂又はその変性樹脂をバインダーにしたホワイト系若しくは透明系の熱又は電子線硬化型接着剤が使用されている。従来のラミネート缶用グラビアインキの代表的な樹脂組成物は、ポリウレタン樹脂、ポリウレタンウレア樹脂、塩化ビニル/酢酸ビニル共重合体樹脂、ポリエステル樹脂及びその混合系、エポキシ樹脂とアセタール樹脂の混合系である。
これらをバインダー樹脂としたグラビアインキを使用したラミネート鋼板を製缶し、3段及び4段ネック加工、樽缶加工等の厳しい加工を行った場合のレトルト処理後における加工部の剥離、ブリスター発生が問題となっている。
【0003】
【発明が解決しようとする課題】
本発明はラミネート金属板に関し、ポリエステルフィルムとインキとの接着部及びインキと接着剤の接着部が熱水並びに水蒸気雰囲気下安定で、特に製缶後のネック加工部に於いて剥離、ブリスターの発生が無い印刷インキ組成物を提供する。
【0004】
【課題を解決するための手段】
本発明者らは、鋭意検討の結果、活性水素を有する樹脂とブロックイソシアネート化合物を含有する印刷インキ組成物が、上記課題を解決することを見出し、本発明に到達した。すなわち、本発明の構成は、活性水素を有する樹脂及びブロックイソシアネート化合物を含有するバインダーを使用することを特徴とするラミネート缶用印刷インキ組成物である。又、本発明の構成は、前記した印刷インキ組成物中のブロックイソシアネート化合物の含有量が1〜20重量%の範囲であるラミネート缶用印刷インキ組成物である。
【0005】
本発明の第二の構成は、前記印刷インキ組成物中に更に有機金属触媒を含有することを特徴とするラミネート缶用印刷インキ組成物である。更に、印刷インキ組成物中の有機金属触媒の含有量が0.1〜1.0重量%の範囲であるラミネート缶用印刷インキ組成物である。
【0006】
更に本発明の構成は、前記した印刷インキ組成物がグラビアインキ又はフレキソインキであるラミネート缶用印刷インキ組成物である。
【0007】
【発明の実施の形態】
本発明の構成は、活性水素を有する樹脂及びブロックイソシアネート化合物を含有するバインダーを使用することを特徴とするラミネート缶用印刷インキ組成物である。活性水素を有する樹脂としてはポリウレタン樹脂、ポリエステル樹脂、ポリウレタンウレア樹脂、塩化ビニル/ビニルアルコール共重合樹脂、酢酸ビニル/ビニルアルコール共重合樹脂、塩化ビニル/酢酸ビニル/ビニルアルコール共重合樹脂、塩化ビニル/酢酸ビニル共重合樹脂、アクリル樹脂、ポリアミド樹脂、硝化綿、エポキシ樹脂、アセタール樹脂、ブチラール樹脂等が挙げられる。これら樹脂は1種類である必要はなく混合しても使用できる。
【0008】
ブロックイソシアネート化合物としては、イソシアヌレート型ポリイソシアネート、ビユーレット型ポリイソシアネート、アダクト型ポリイソシアネートの末端イソシアネート基をブロック剤でマスクした物を使用する。前記ブロックイソシアネート化合物の原料である有機ジイソシアネートとして好ましい物は、1,6−ヘキサメチレンジイソシアネート、イソホロンジイソシアネート、4,4’−ジフェニルメタンジイソシアネート、キシリレンジイソシアネート、トリレンジイソシアネート、ナフチレンジイソシアネート及びこれらの混合物が挙げられる。
【0009】
ブロック化剤としては、活性メチレン化合物としてマロン酸ジエステル、アセト酢酸エステル、アセチルアセトン等が、オキシム化合物としてアセトオキシム、ケトオキシム(メチルエチルケトオキシム、ブタノンオキシム)等が、フェノール化合物としてフェノール、クレゾール等が、ラクタム化合物としてεカプロラクタム等が、イミダゾール化合物として2−メチルイミダゾール等が挙げられる。ブロック化剤としては必ずしも1種類である必要はなく混合しても使用できる。
【0010】
印刷インキ組成物中のブロックイソシアネート化合物の添加量は1〜20重量%の範囲、より好ましくは2〜10重量%の範囲にする事により、製缶焼き付け後のフィルム及び接着剤層との密着性が向上し、特にインキを厚盛り若しくは積層し、厳しい加工を施した後のレトルト耐性が向上する。ブロックイソシアネート化合物の添加量が1重量%を下回る場合、製缶焼き付け後のフィルム及び接着剤層との密着性向上に対する寄与が低下する。又逆にブロックイソシアネート化合物の添加量が20重量%を上回る場合、印刷時におけるガイドロール取られ、巻き取り時に於けるブロッキングの問題が発生する場合がある。
【0011】
有機金属触媒は、ブロックイソシアネート化合物のブロック剤解離を促進し、活性水素を有する樹脂との反応性を向上する為に使用することができる。有機金属触媒としては、オクチル酸亜鉛、ジオクチル錫ジアセテート(DOTDA)、ジブチル錫ジラウレート(DBTDL)、ジブチル錫ジアセテート(DBTDA)等が挙げられる。印刷インキ組成物中の有機金属触媒の添加量は、0.1〜1.0重量%の範囲、より好ましくは0.2〜0.5重量%の範囲にする事により触媒未使用の場合と比較して更にフィルム及び接着剤層との密着性が向上し、特にインキを厚盛り若しくは積層し、厳しい加工を施した後のレトルト耐性が向上する。触媒の添加量が0.1重量%を下回ると、触媒未使用の場合と性能的に差がなくなる。逆に触媒の添加量が1.0重量%を上回ると活性水素を有するバインダー樹脂の化学結合(ウレタン結合、エステル結合、ウレア結合等)の切断が発生、経時的に粘度低下する問題が有る。
【0012】
使用される金属板としては、亜鉛メッキ鋼板、クロムメッキ鋼板、錫メッキ鋼板、ニッケルメッキ鋼板、アルミメッキ鋼板、その他各種合金メッキ鋼板、ステンレススチール、アルミニウム板、銅板、チタン板、又必要に応じてそれらにリン酸処理、クロメート処理、有機クロメート処理、コバルト複合酸化膜処理等を行った物を用いることも出来る。
【0013】
利用可能なプラスチックフィルムとしては、ポリエステル樹脂フィルムが特に好ましいが、その他のポリプロピレン、ナイロン、ポリエチレン樹脂フィルムなどに対しても用いることが出来る。
【0014】
【実施例】
以下、実施例を用い具体的に説明するが、本発明はこれに限定されるものではない。尚、実施例における部とは重量部を示す。
【0015】
[実施例1]
酸化チタン30部、ポリウレタンウレア樹脂(バーノックL4−079、大日本インキ化学工業製)35部、メチルエチルケトン21部、トルエン14部を通常法で練肉し、白色印刷インキ(A)を製造した。この白色印刷インキ(A)100部に対して、ヘキサメチレンジイソシアネートを原料にしたイソシアヌレート型ポリイソシアネートの末端イソシアネート基をメチルエチルケトオキシムでブロックしたブロックイソシアネート化合物〔ブロックイソシアネート化合物(A)、有効NCO%=6.5%〕2部を添加し、攪拌混合して印刷インキを調整した。この印刷インキを所定の希釈溶剤にて17秒(ザーンカップNO3)に調整後、版深25ミクロンのグラビア版を備えた印刷機にてポリエステルフィルムに印刷(1度刷り、2度刷り)、乾燥して印刷フィルムを得た。次に、前記印刷面に電子線及び熱硬化型ホワイト接着剤を塗布量11g/m2(ドライ)になる様塗工、乾燥後室温にて7日間エージングした。次に、この塗工フィルムと錫メッキ鋼板を180℃の熱ロールを用いて熱圧着後、加速電圧165KV、電流値3mAで30KGyの電子線照射を行い、更に215℃、90秒の焼き付けを行ってポリエステルフィルム被覆鋼板を作成した。
【0016】
[実施例2]
白色印刷インキ(A)100部に対して、ブロックイソシアネート化合物(A)10部を添加し、攪拌混合して印刷インキを調整した。以下、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0017】
[実施例3]
白色印刷インキ(A)100部に対して、ブロックイソシアネート化合物(A)、2部、ジブチル錫ジアセテート(DBTDA)0.05部を添加し、攪拌混合して印刷インキを調整した。以下、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0018】
[実施例4]
白色印刷インキ(A)100部に対して、ブロックイソシアネート化合物(A)、2部、ジブチル錫ジアセテート(DBTDA)0.3部を添加し、攪拌混合して印刷インキを調整した。以下、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0019】
[実施例5]
白色印刷インキ(A)100部に対して、ブロックイソシアネート化合物(A)、10部、ジブチル錫ジアセテート(DBTDA)0.3部を添加し、攪拌混合して印刷インキを調整した。以下、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0020】
[実施例6]
白色印刷インキ(A)100部に対して、ブロックイソシアネート化合物(A)2部、ジブチル錫ジラウレート(DBTDL)0.3部を添加し、攪拌混合して印刷インキを調整した。以下、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0021】
[実施例7]
白色印刷インキ(A)100部に対して、ヘキサメチレンジイソシアネートを原料にしたイソシアヌレート型ポリイソシアネートの末端イソシアネート基を活性メチレン化合物でブロックしたブロックイソシアネート化合物〔ブロックイソシアネート化合物(B)、有効NCO%=6.6%〕2部を添加し、攪拌混合して印刷インキを調整した。以下、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0022】
[実施例8]
白色印刷インキ(A)100部に対して、ブロックイソシアネート化合物(B)2部、ジブチル錫ジアセテート(DBTDA)0.3部を添加し、攪拌混合して印刷インキを調整した。以下、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0023】
[実施例9]
白色印刷インキ(A)100部に対して、ブロックイソシアネート化合物(B)10部、ジブチル錫ジアセテート(DBTDA)0.3部を添加し、攪拌混合して印刷インキを調整した。以下、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0024】
[実施例10]
白色印刷インキ(A)100部に対して、ブロックイソシアネート化合物(A)0.05部添加し、攪拌混合して印刷インキを調整した。以下、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0025】
[比較例1]
白色印刷インキ(A)のみを使用して、実施例1と同条件にてポリエステルフィルム被覆鋼板を作成した。
【0026】
実施例1〜10及び比較例1で得られたポリエステルフィルム被覆鋼板について性能評価を行い、結果を表1、表2に示した。尚、各性能評価の条件は下記の通りである。
【0027】
[被覆外観]
作成したポリエステルフィルム被覆鋼板を125℃、30分のレトルト処理を行い、外観(ブリスターの発生、フィルムの皺等)を拡大鏡又は目視により5段階で評価した。非常に良好(◎)、良好(○)、僅かに不良(△)、不良(×)、非常に不良(××)とし、合格レベルは◎、○である。
【0028】
[ネック加工性]
作成したポリエステルフィルム被覆鋼板を、代用試験として、深絞りエリクセン機を使用して直径25mm、高さ8mm及び高さ12mmに絞り、125℃、30分のレトルト処理を行い、上記同様5段階で評価した。「高さ8mm絞り」が、概ね3段ネック加工に、「高さ12mm絞り」が概ね4段ネック加工に相当する。
【0029】
【表1】

Figure 0004058855
【0030】
【表2】
Figure 0004058855
【0031】
Figure 0004058855
【0032】
上記実験結果より、本発明の印刷インキ組成物は製缶焼き付け後のフィルム及び接着剤層との密着性が向上し、特にインキを積層し厳しいネック加工を施した後のレトルト耐性が向上しているのがわかる。
【0033】
【発明の効果】
本発明の印刷インキ組成物を使用する事で、従来困難であった3段及び4段ネック加工、樽缶加工等の厳しい加工を行った場合のレトルト処理後に於ける加工部の剥離、ブリスター発生等が解消でき、意匠性に優れたラミネート缶の製造を可能にした。[0001]
BACKGROUND OF THE INVENTION
The present invention is used for laminated metal plates used for heat resistance, cosmetics, corrosion resistance, rust prevention of metal can materials such as beverage cans such as soft drinks, coffee, tea, tea, beer, canned goods, aerosol cans, and art cans. The present invention relates to a printing ink composition.
[0002]
[Prior art]
Laminated metal plate method has been practical since several years ago. Gravure printing is applied to a polyester film and bonded to a metal plate with an adhesive due to advantages such as high productivity, excellent flavor, environmental hormone countermeasures, and clear printing effects. It has become. As the adhesive, a white or transparent heat or electron beam curable adhesive using an epoxy, polyester, polyurethane resin or a modified resin thereof as a binder is used. Typical resin compositions of conventional gravure inks for laminate cans are polyurethane resins, polyurethane urea resins, vinyl chloride / vinyl acetate copolymer resins, polyester resins and mixed systems thereof, and mixed systems of epoxy resins and acetal resins. .
Laminated steel plates using gravure inks with these binder resins can be made, and peeling of processed parts and blistering after retort processing when severe processing such as 3-step and 4-step neck processing and barrel processing is performed It is a problem.
[0003]
[Problems to be solved by the invention]
TECHNICAL FIELD The present invention relates to a laminated metal plate, and a bonded portion of a polyester film and an ink and a bonded portion of an ink and an adhesive are stable in a hot water and water vapor atmosphere. There is provided a printing ink composition having no ink.
[0004]
[Means for Solving the Problems]
As a result of intensive studies, the present inventors have found that a printing ink composition containing a resin having active hydrogen and a blocked isocyanate compound solves the above problems, and has reached the present invention. That is, the constitution of the present invention is a printing ink composition for laminate cans characterized by using a binder containing a resin having active hydrogen and a blocked isocyanate compound. Moreover, the structure of this invention is the printing ink composition for laminated cans whose content of the block isocyanate compound in an above described printing ink composition is the range of 1-20 weight%.
[0005]
According to a second aspect of the present invention, there is provided a printing ink composition for laminate cans, wherein the printing ink composition further contains an organometallic catalyst. Furthermore, it is a printing ink composition for laminate cans in which the content of the organometallic catalyst in the printing ink composition is in the range of 0.1 to 1.0% by weight.
[0006]
Furthermore, the structure of this invention is a printing ink composition for laminated cans whose above-mentioned printing ink composition is gravure ink or flexographic ink.
[0007]
DETAILED DESCRIPTION OF THE INVENTION
The constitution of the present invention is a printing ink composition for laminate cans characterized by using a binder containing a resin having active hydrogen and a blocked isocyanate compound. Examples of the resin having active hydrogen include polyurethane resin, polyester resin, polyurethane urea resin, vinyl chloride / vinyl alcohol copolymer resin, vinyl acetate / vinyl alcohol copolymer resin, vinyl chloride / vinyl acetate / vinyl alcohol copolymer resin, vinyl chloride / Examples thereof include vinyl acetate copolymer resin, acrylic resin, polyamide resin, nitrified cotton, epoxy resin, acetal resin, butyral resin. These resins do not need to be one kind and can be used even if mixed.
[0008]
As the blocked isocyanate compound, an isocyanurate type polyisocyanate, a biuret type polyisocyanate, or an adduct type polyisocyanate obtained by masking the terminal isocyanate group with a blocking agent is used. Preferred examples of the organic diisocyanate that is the raw material of the blocked isocyanate compound include 1,6-hexamethylene diisocyanate, isophorone diisocyanate, 4,4′-diphenylmethane diisocyanate, xylylene diisocyanate, tolylene diisocyanate, naphthylene diisocyanate, and mixtures thereof. Can be mentioned.
[0009]
As the blocking agent, malonic acid diester, acetoacetate ester, acetylacetone, etc. as active methylene compounds, acetooxime, ketoxime (methyl ethyl ketoxime, butanone oxime), etc. as oxime compounds, phenol, cresol, etc. as lactose compounds, lactam compounds Ε caprolactam and the like, and imidazole compounds include 2-methylimidazole and the like. The blocking agent is not necessarily one type, and can be used even if mixed.
[0010]
The addition amount of the blocked isocyanate compound in the printing ink composition is in the range of 1 to 20% by weight, more preferably in the range of 2 to 10% by weight, so that the adhesiveness with the film and the adhesive layer after can baking is made. In particular, the resistance to retort is improved after the ink is thickened or laminated and subjected to severe processing. When the addition amount of a block isocyanate compound is less than 1 weight%, the contribution with respect to the adhesive improvement with the film and adhesive layer after can-baking will fall. On the other hand, if the amount of the blocked isocyanate compound exceeds 20% by weight, the guide roll may be removed during printing, and blocking may occur during winding.
[0011]
The organometallic catalyst can be used for promoting the dissociation of the blocking agent of the blocked isocyanate compound and improving the reactivity with the resin having active hydrogen. Examples of the organometallic catalyst include zinc octylate, dioctyltin diacetate (DOTDA), dibutyltin dilaurate (DBTDL), and dibutyltin diacetate (DBTDA). The addition amount of the organometallic catalyst in the printing ink composition is in the range of 0.1 to 1.0% by weight, more preferably in the range of 0.2 to 0.5% by weight. In comparison, the adhesion to the film and the adhesive layer is further improved, and in particular, the resistance to retort is improved after the ink is thickened or laminated and subjected to severe processing. When the addition amount of the catalyst is less than 0.1% by weight, there is no difference in performance from the case where the catalyst is not used. On the other hand, when the amount of the catalyst added exceeds 1.0% by weight, there is a problem in that the chemical bond (urethane bond, ester bond, urea bond, etc.) of the binder resin having active hydrogen is broken and the viscosity decreases with time.
[0012]
As the metal plate used, galvanized steel plate, chrome plated steel plate, tin plated steel plate, nickel plated steel plate, aluminum plated steel plate, other various alloy plated steel plates, stainless steel, aluminum plate, copper plate, titanium plate, and as required Those subjected to phosphoric acid treatment, chromate treatment, organic chromate treatment, cobalt composite oxide film treatment and the like can also be used.
[0013]
As a usable plastic film, a polyester resin film is particularly preferable, but it can also be used for other polypropylene, nylon, polyethylene resin films and the like.
[0014]
【Example】
Hereinafter, the present invention will be specifically described with reference to examples, but the present invention is not limited thereto. In addition, the part in an Example shows a weight part.
[0015]
[Example 1]
30 parts of titanium oxide, 35 parts of polyurethane urea resin (Bernock L4-079, manufactured by Dainippon Ink and Chemicals), 21 parts of methyl ethyl ketone, and 14 parts of toluene were kneaded by a conventional method to produce a white printing ink (A). With respect to 100 parts of this white printing ink (A), a blocked isocyanate compound in which the terminal isocyanate group of an isocyanurate type polyisocyanate using hexamethylene diisocyanate as a raw material is blocked with methyl ethyl ketoxime [block isocyanate compound (A), effective NCO% = 6.5%] 2 parts were added and mixed with stirring to prepare a printing ink. This printing ink is adjusted to 17 seconds (Zahn cup NO3) with a predetermined dilution solvent, then printed on a polyester film with a printing machine equipped with a gravure plate with a plate depth of 25 microns (printed once and twice) and dried. A printed film was obtained. Next, the printed surface was coated with an electron beam and a thermosetting white adhesive so as to have a coating amount of 11 g / m 2 (dry), dried and then aged at room temperature for 7 days. Next, the coated film and the tin-plated steel sheet are thermocompression-bonded using a 180 ° C. hot roll, irradiated with an electron beam of 30 KGy at an acceleration voltage of 165 KV and a current value of 3 mA, and further baked at 215 ° C. for 90 seconds. A polyester film-coated steel sheet was prepared.
[0016]
[Example 2]
To 100 parts of the white printing ink (A), 10 parts of the blocked isocyanate compound (A) was added and mixed by stirring to adjust the printing ink. Hereinafter, a polyester film-coated steel sheet was prepared under the same conditions as in Example 1.
[0017]
[Example 3]
To 100 parts of the white printing ink (A), 2 parts of the blocked isocyanate compound (A) and 0.05 part of dibutyltin diacetate (DBTDA) were added and mixed by stirring to adjust the printing ink. Hereinafter, a polyester film-coated steel sheet was prepared under the same conditions as in Example 1.
[0018]
[Example 4]
To 100 parts of the white printing ink (A), 2 parts of the blocked isocyanate compound (A) and 0.3 part of dibutyltin diacetate (DBTDA) were added and mixed by stirring to adjust the printing ink. Hereinafter, a polyester film-coated steel sheet was prepared under the same conditions as in Example 1.
[0019]
[Example 5]
To 100 parts of the white printing ink (A), 10 parts of the blocked isocyanate compound (A) and 0.3 part of dibutyltin diacetate (DBTDA) were added and mixed by stirring to prepare the printing ink. Hereinafter, a polyester film-coated steel sheet was prepared under the same conditions as in Example 1.
[0020]
[Example 6]
To 100 parts of the white printing ink (A), 2 parts of the blocked isocyanate compound (A) and 0.3 part of dibutyltin dilaurate (DBTDL) were added and mixed by stirring to adjust the printing ink. Hereinafter, a polyester film-coated steel sheet was prepared under the same conditions as in Example 1.
[0021]
[Example 7]
Block isocyanate compound [block isocyanate compound (B), effective NCO% = blocked isocyanate compound in which terminal isocyanate group of isocyanurate type polyisocyanate using hexamethylene diisocyanate as a raw material was blocked with 100 parts of white printing ink (A) 6.6%] 2 parts were added and mixed with stirring to prepare a printing ink. Hereinafter, a polyester film-coated steel sheet was prepared under the same conditions as in Example 1.
[0022]
[Example 8]
To 100 parts of the white printing ink (A), 2 parts of the blocked isocyanate compound (B) and 0.3 part of dibutyltin diacetate (DBTDA) were added and mixed by stirring to adjust the printing ink. Hereinafter, a polyester film-coated steel sheet was prepared under the same conditions as in Example 1.
[0023]
[Example 9]
To 100 parts of the white printing ink (A), 10 parts of the blocked isocyanate compound (B) and 0.3 part of dibutyltin diacetate (DBTDA) were added and mixed by stirring to adjust the printing ink. Hereinafter, a polyester film-coated steel sheet was prepared under the same conditions as in Example 1.
[0024]
[Example 10]
To 100 parts of the white printing ink (A), 0.05 part of the blocked isocyanate compound (A) was added and mixed by stirring to adjust the printing ink. Hereinafter, a polyester film-coated steel sheet was prepared under the same conditions as in Example 1.
[0025]
[Comparative Example 1]
A polyester film-coated steel sheet was prepared under the same conditions as in Example 1 using only the white printing ink (A).
[0026]
Performance evaluation was performed on the polyester film-coated steel plates obtained in Examples 1 to 10 and Comparative Example 1, and the results are shown in Tables 1 and 2. The conditions for each performance evaluation are as follows.
[0027]
[Coating appearance]
The prepared polyester film-coated steel sheet was subjected to a retort treatment at 125 ° C. for 30 minutes, and the appearance (blister generation, film wrinkles, etc.) was evaluated in five stages by a magnifying glass or visual observation. Very good (◎), good (◯), slightly bad (Δ), bad (×), very bad (XX), and pass levels are ◎ and ○.
[0028]
[Neck workability]
As a substitute test, the prepared polyester film-coated steel sheet was drawn to a diameter of 25 mm, a height of 8 mm and a height of 12 mm using a deep drawing Erichsen machine, subjected to retort treatment at 125 ° C. for 30 minutes, and evaluated in the same manner as above. did. “Height 8 mm aperture” generally corresponds to 3-step neck processing, and “Height 12 mm aperture” generally corresponds to 4-step neck processing.
[0029]
[Table 1]
Figure 0004058855
[0030]
[Table 2]
Figure 0004058855
[0031]
Figure 0004058855
[0032]
From the above experimental results, the printing ink composition of the present invention has improved adhesion to the film and the adhesive layer after can-baking, particularly improved retort resistance after laminating the ink and subjecting it to severe neck processing. I can see that
[0033]
【The invention's effect】
By using the printing ink composition of the present invention, peeling of processed parts and blistering after retort processing when severe processing such as three-step and four-step neck processing and barrel can processing, which has been difficult in the past, are performed. This makes it possible to produce laminated cans with excellent design.

Claims (4)

活性水素を有する樹脂ブロックイソシアネート化合物を含有するバインダー及び有機金属触媒を含有することを特徴とするラミネート缶用印刷インキ組成物。A printing ink composition for laminate cans , comprising a resin having active hydrogen, a binder containing a blocked isocyanate compound, and an organometallic catalyst . 前記した印刷インキ組成物中のブロックイソシアネート化合物の含有量が1〜20重量%の範囲である請求項1に記載のラミネート缶用印刷インキ組成物。  The printing ink composition for laminate cans according to claim 1, wherein the content of the blocked isocyanate compound in the printing ink composition is in the range of 1 to 20% by weight. 印刷インキ組成物中の有機金属触媒の含有量が0.1〜1.0重量%の範囲である請求項1又は2に記載のラミネート缶用印刷インキ組成物。  The printing ink composition for laminate cans according to claim 1 or 2, wherein the content of the organometallic catalyst in the printing ink composition is in the range of 0.1 to 1.0% by weight. 前記した印刷インキ組成物がグラビアインキ又はフレキソインキである請求項1〜3の何れかに記載のラミネート缶用印刷インキ組成物。  The printing ink composition for laminate cans according to any one of claims 1 to 3, wherein the printing ink composition is a gravure ink or a flexo ink.
JP27422799A 1999-09-28 1999-09-28 Printing ink composition for laminate cans Expired - Lifetime JP4058855B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27422799A JP4058855B2 (en) 1999-09-28 1999-09-28 Printing ink composition for laminate cans

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27422799A JP4058855B2 (en) 1999-09-28 1999-09-28 Printing ink composition for laminate cans

Publications (2)

Publication Number Publication Date
JP2001098192A JP2001098192A (en) 2001-04-10
JP4058855B2 true JP4058855B2 (en) 2008-03-12

Family

ID=17538800

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27422799A Expired - Lifetime JP4058855B2 (en) 1999-09-28 1999-09-28 Printing ink composition for laminate cans

Country Status (1)

Country Link
JP (1) JP4058855B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4536487B2 (en) * 2004-11-09 2010-09-01 ブリヂストンスポーツ株式会社 Golf ball ink, golf ball transfer film and marked golf ball
JP5137437B2 (en) * 2007-03-29 2013-02-06 日本クラウンコルク株式会社 Painted metal plate and cap made of the same

Also Published As

Publication number Publication date
JP2001098192A (en) 2001-04-10

Similar Documents

Publication Publication Date Title
JP6032279B2 (en) Polyester resin, resin composition for can coating, painted metal plate for can and can
US5147729A (en) Steel plate with organic coating having improved corrosion resistance in as-worked state
JP2000290630A (en) Polyurethane adhesive composition
JP2004269679A (en) Adhesive, method for producing the adhesive, and plastic film-laminated steel sheet
JPS5937029B2 (en) Cathode electrodeposition coating method
JP6981238B2 (en) Resin composition, laminate, and beverage cans using it
JP4254182B2 (en) Adhesive and its use
JP4058855B2 (en) Printing ink composition for laminate cans
AU600374B2 (en) One-can heat-curable resin compositions and precoated metal
JPS63301217A (en) One-pack thermosetting resin composition and precoated metal
JP4533598B2 (en) Paint for metal packaging body and metal packaging body using the same
JPH0243272A (en) Resin composition for chipping-resistant coating material
JP4015252B2 (en) Polyester film bonded metal plate adhesive
JPH08199147A (en) Laminating adhesive composition and metal plate laminating film using the same
JP2002179998A (en) Coating composition and coated steel sheet using the same
JP4238511B2 (en) Adhesive and its use
EP1099542B1 (en) Plastic-coated metal plate
US20240084164A1 (en) Cationic electrodeposition coating composition and method for forming cured electrodeposition coating film
EP1448652B1 (en) Polyisocyanates that are blocked by mixing with t-caprolactam and dipa or 1,2,4-triazole, their production and use thereof
JPH03237173A (en) One-pack thermosetting resin composition and precoated metal using same
JP2001107015A (en) Thermosetting adhesive
JPH11181392A (en) Adhesive composition for laminated can, and laminated metal sheet
JP4207410B2 (en) Adhesive and its use
JP3424141B2 (en) Cationic electrodeposition coating composition containing reactive surface smoothing agent
DE19532063A1 (en) Binders containing isocyanurate polyisocyanates based on 1,4-diisocyanatobutane and their use for coating substrates

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20040907

RD01 Notification of change of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7421

Effective date: 20050624

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20070810

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20070823

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20071016

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20071127

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20071210

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101228

Year of fee payment: 3

R150 Certificate of patent or registration of utility model

Ref document number: 4058855

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101228

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111228

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111228

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121228

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121228

Year of fee payment: 5

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121228

Year of fee payment: 5

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121228

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121228

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131228

Year of fee payment: 6

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

EXPY Cancellation because of completion of term