JP3399485B2 - Heat melting type road marking paint - Google Patents

Heat melting type road marking paint

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Publication number
JP3399485B2
JP3399485B2 JP05643194A JP5643194A JP3399485B2 JP 3399485 B2 JP3399485 B2 JP 3399485B2 JP 05643194 A JP05643194 A JP 05643194A JP 5643194 A JP5643194 A JP 5643194A JP 3399485 B2 JP3399485 B2 JP 3399485B2
Authority
JP
Japan
Prior art keywords
resin
paint
polystyrene
block copolymer
weight
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
JP05643194A
Other languages
Japanese (ja)
Other versions
JPH07258583A (en
Inventor
辰夫 東郷
武 廣田
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.)
Sekisui Jushi Corp
Original Assignee
Sekisui Jushi Corp
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 Sekisui Jushi Corp filed Critical Sekisui Jushi Corp
Priority to JP05643194A priority Critical patent/JP3399485B2/en
Publication of JPH07258583A publication Critical patent/JPH07258583A/en
Application granted granted Critical
Publication of JP3399485B2 publication Critical patent/JP3399485B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Road Signs Or Road Markings (AREA)
  • Paints Or Removers (AREA)

Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明はコンクリートやアスファ
ルト路面等に種々の道路標示をするのに使用される加熱
溶融型道路標示塗料に関するものである。 【0002】 【従来の技術】従来、加熱溶融型道路標示塗料は、石油
樹脂等の粘結樹脂に、酸化チタン等の顔料、炭酸カルシ
ウム等の充填剤等が配合されると共に、ガラスビーズが
混入されている。又、ガラスビーズは一般に塗料全体に
対して15〜18重量%程度混入され、路面に塗布した
塗膜表面に突出してその再帰反射性を利用して夜間の視
認性を高めるようになされている。 【0003】 【発明が解決しようとする課題】しかしながら、かかる
従来の加熱溶融型道路標示塗料は、ガラスビーズの混入
量が15〜18重量%と低いため、路面に塗布した塗膜
が車両の通行により摩耗すると、塗膜表面に突出したガ
ラスビーズがほとんどなくなり、夜間の視認性が著しく
低下する問題点があった。又、塗料は単に粘結樹脂に顔
料、充填剤等が配合され、とくに耐摩耗性の配合となさ
れておらず、交通量の多い道路においては塗膜の摩耗の
進行が速く、上記夜間の視認性が長期に亘って維持でき
ない問題点があった。 【0004】本発明はかかる従来の問題点を解消した加
熱溶融型道路標示塗料を提供することを目的としてい
る。 【0005】 【課題を解決するための手段】上記課題を解決するた
め、本発明は、従来汎用の加熱溶融型道路標示塗料にポ
リスチレン−ポリイソプレンブロック共重合樹脂又はポ
リスチレン−ポリブタジエンブロック共重合樹脂又はこ
れらの混合樹脂又は非晶性ポリアルファオレフィン樹脂
の粘接着性樹脂を所定量配合することにより、塗料の物
質間の密着力を高めて柔軟性を付与し耐衝撃性を高め、
耐摩耗性に寄与するようにし、さらにガラスビーズの混
入量を増やすことにより、夜間の視認性とくに摩耗時の
視認性を向上させたものである。 【0006】すなわち、本発明加熱溶融型道路標示塗料
は、粘結樹脂、顔料、充填剤等からなる加熱溶融型道路
標示塗料において、粘結樹脂は塗料全体に対して10〜
20重量%配合され、粘接着性樹脂が塗料全体に対して
1〜15重量%配合され、ガラスビーズが塗料全体に対
して30〜60重量%混入されてなり、上記粘接着性樹
脂がポリスチレン−ポリイソプレンブロック共重合樹脂
又はポリスチレン−ポレブタジエンブロック共重合樹脂
又はこれらの混合樹脂又は非晶性ポリアルファオレフィ
ン樹脂であるものである。 【0007】本発明に配合される粘結樹脂としては、従
来汎用のものが使用されればよい。一般には石油樹脂が
使用されるが、生ロジン、マレイン化ロジン、マレイン
化ロジンエステル、ポリアミド樹脂、不飽和ポリエステ
ル樹脂、キシレン樹脂等の熱可塑性樹脂が使用されても
よい。粘結樹脂の配合割合は塗料全体に対して10〜2
0重量%とする。この配合割合は、10重量%以下では
塗料の流動性、接着性に劣り、20重量%以上では塗膜
の耐汚染性が悪くなことから10〜20重量%とする。 【0008】顔料としては、二酸化チタン、亜鉛華、リ
トポン等の白色顔料、黄鉛、チタンイエロー等の黄色顔
料等従来汎用のものが使用される。顔料の配合割合は塗
料全体に対して2〜10重量%が好ましい。この配合割
合は、2重量%以下では着色力、隠蔽力が小さく、10
重量%以上であってもそれ以上効果が上がらずコスト高
となるだけであることから2〜10重量%が好ましい。 【0009】充填剤としては、炭酸カルシウム、珪砂、
寒水砂、タルク等従来汎用のものが使用される。充填剤
の配合割合は塗料全体に対して30〜50重量%が好ま
しい。この配合割合は、30重量%以下では塗膜の耐汚
染性や耐摩耗性に劣り、50重量%以上では塗膜の接着
性の低下、クラック発生が起こることから30〜50重
量%が好ましい。 【0010】本発明に配合される粘接着性樹脂は、その
接着力により塗料の物質間の密着性を良好にし、塗膜に
柔軟性を付与して耐衝撃性を高めるためのものであっ
て、ポリスチレン−ポリイソプレンブロック共重合樹脂
又はポリスチレン−ポリブタジエンブロック共重合樹脂
又はこれらの混合樹脂からなるスチレン系ブロック共重
合樹脂、あるいは又非晶性ポリアルファオレフィン樹脂
が好適に使用される。 【0011】上記ポリスチレン−ポリイソプレンブロッ
ク共重合樹脂、ポリスチレン−ポリブタジエンブロック
共重合樹脂のスチレン系ブロック共重合樹脂は、粘接着
性を有する熱可塑性エラストマーであって、溶融粘度の
低いものである。溶融粘度が低いことから塗料のホット
メルト工法による作業性がよく、溶融粘度が低いにもか
かわらず塗料の軟化点をそのまま維持できる利点を有し
ている。又、ポリスチレン−ポリイソプレンブロック共
重合樹脂、ポリスチレン−ポリブタジエンブロック共重
合樹脂は適宜割合で混合されてもよく、上記性質を損な
うことなく好適に使用できる。 【0012】上記非晶性ポリアルファオレフィン樹脂
は、プロピレンとエチレン又はブレン−1を共重合した
比較的分子量の低い樹脂である。一般に単独でホットメ
ルト接着剤やシーリング剤として利用できるものであ
り、粘結樹脂とくに石油樹脂との接着性、相溶性に優れ
ていることから、分子間の結合力を高めて塗膜に柔軟性
を付与して耐衝撃性を高めることができるものである。 【0013】粘接着性樹脂の配合割合は塗料全体に対し
て1〜15重量%が好ましい。この配合割合は、1重量
%以下では塗膜に十分な耐摩耗性が得られず、15重量
%以上では塗料の流動性が悪くなり施工性が悪く、塗膜
のエッジが乱れ整った標示が得られないことから1〜1
5重量%が好ましい。とくに、2重量%を越えると次第
に流動性が悪くなって施工性が低下し、良好な標示が得
がたいことから1〜2重量%がより好ましい。 【0014】又、ガラスビーズの混入量は塗料全体に対
して30〜60重量%が好ましい。この混入量は、30
重量%以下では塗膜の摩耗時の反射輝度が不十分となり
夜間視認性に劣り、60重量%以上ではコスト高になる
と共に塗膜形成に支障をきたすことから30〜60重量
%が好ましい。とくに、塗膜の摩耗時の十分な反射輝度
を確保し、施工や塗膜形成が良好な面から40〜50重
量%がより好ましい。又、ガラスビーズとしては通常粒
径60〜710μm、屈折率1.5以上のものが使用さ
れ、とくに高輝度ガラスビーズが使用されると夜間の視
認性がより向上し好ましい。 【0015】なお、本発明には上記以外に、添加剤とし
て酸化防止剤や沈降防止剤のワックス、あるいは植物
油、植物油変性アルキド樹脂、フタル酸エステル等の可
塑剤等が必要に応じて適宜量配合されてもよい。 【0016】 【実施例】以下、本発明の実施例について述べる。粘結
樹脂(石油樹脂)、顔料(酸化チタン)、充填剤(炭酸
カルシウム)、ガラスビーズ、添加剤(ワックス、可塑
剤)からなり、ガラスビーズの混入量を変えた表1に示
す3種類の塗料(No.1〜No.3)を用い、これら
塗料をそれぞれ約200℃の温度で溶融し、アルミニウ
ム板上に均一に塗布して幅15cm、長さ50cm、厚
み2.0mmの塗膜を形成した。 【0017】アスコンブラストキャビネットBA−1型
直圧式機械(厚地鉄工社製)により東芝バロティーニ社
製プラショットTSP60を用いて約1分間上記塗膜表
面を均一に摩耗させ、摩耗後の塗膜の乾燥時と湿潤時に
ついて任意10箇所の反射輝度を輝度測定器により測定
し、その結果を表2に示した。なお、上記摩耗試験はタ
イヤによる摩耗を再現すべくサンドブラストとして樹脂
粉体を用い、ガラスビーズの破壊を起こすことなく均一
に摩耗させた。 【0018】 【表1】 【0019】 【表2】 【0020】表1、表2によりガラスビーズの混入量の
増加に伴い摩耗後の反射輝度値が順次高くなることが確
認できた。次に、とくに混入量30重量%以上のNo.
3の塗料を基本として、ポリスチレン−ポリイソプレン
ブロック共重合樹脂、ポリスチレン−ポリブタジエンブ
ロック共重合樹脂、非晶性ポリアルファオレフィン樹脂
の粘接着性樹脂の配合による塗膜の耐摩耗性について調
べた。 【0021】粘結樹脂(石油樹脂)、顔料(酸化チタ
ン)、充填剤(炭酸カルシウム)、ガラスビーズ、添加
剤(ワックス、可塑剤)からなり、これにポリスチレン
−ポリイソプレンブロック共重合樹脂(SIS)(日本
ゼオン社製クインタック3421)の配合量を変えた表
3に示す4種類の塗料(実施例1〜3、比較例2)とポ
リスチレン−ポリイソプレンブロック共重合樹脂を配合
しない塗料(比較例1)を用い、これら塗料をそれぞれ
約200℃の温度で溶融し、JIS K 5665 3
種の耐摩耗性試験方法に準じて試験し、その結果(摩耗
減量)を表3に示した。 【0022】 【表3】【0023】粘結樹脂(石油樹脂)、顔料(酸化チタ
ン)、充填剤(炭酸カルシウム)、ガラスビーズ、添加
剤(ワックス、可塑剤)からなり、これにポリスチレン
−ポリブタジエンブロック共重合樹脂(SBS)(日本
ゼオン社製クインタックBL−301)の配合量を変え
た表4に示す4種類の塗料(実施例4〜6、比較例3)
とポリスチレン−ポリブタジエンブロック共重合樹脂を
配合しない塗料(比較例1)を用い、上記と同様の試験
結果を表4に示した。 【0024】 【表4】 【0025】粘結樹脂(石油樹脂)、顔料(酸化チタ
ン)、充填剤(炭酸カルシウム)、ガラスビーズ、添加
剤(ワックス、可塑剤)からなり、これに非晶性ポリア
ルファオレフィン樹脂(APAO)(宇部レキセン社製
ウベタックUT2585)の配合量を変えた表5に示す
4種類の塗料(実施例7〜9、比較例4)と非晶性ポリ
アルファオレフィン樹脂を配合しない塗料(比較例1)
を用い、上記と同様の試験結果を表5に示した。 【0026】 【表5】 【0027】表3〜5からわかるように比較例1〜4に
おいては摩耗減量が大きく、実施例1〜9においては摩
耗減量が少ないことが確認できた。又、ポリスチレン−
ポリイソプレンブロック共重合樹脂、ポリスチレン−ポ
リブタジエンブロック共重合樹脂、非晶性ポリアルファ
オレフィン樹脂の配合量がそれぞれ2重量%の実施例
3、実施例6、実施例9においては、他の実施例に比べ
塗料の流動性がやや低下し、塗膜表面に粘着感が少しあ
った。 【0028】 【発明の効果】以上詳述した如く、本発明加熱溶融型道
路標示塗料は、ポリスチレン−ポリイソプレンブロック
共重合樹脂又はポリスチレン−ポリブタジエンブロック
共重合樹脂又はこれらの混合樹脂又は非晶性ポリアルフ
ァオレフィン樹脂の粘接着性樹脂が塗料全体に対して1
〜15重量%配合されているので、従来に比べて路面に
塗布形成した塗膜の耐摩耗性を向上させることができ
る。 【0029】又、ガラスビーズが塗料全体に対して30
〜60重量%混入されているので、上記粘接着性樹脂が
配合されていることと相まってガラスビーズが塗膜から
剥離しがたく、夜間視認性を向上させることができる。
しかも、塗膜の摩耗時にたとえ多少剥離しても夜間視認
性を良好な状態で保ち、長期に亘ってその反射性能を維
持できる。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hot-melt type road marking paint used for marking various roads on concrete and asphalt road surfaces. 2. Description of the Related Art Conventionally, a hot-melt type road marking paint contains a binder resin such as a petroleum resin, a pigment such as titanium oxide, a filler such as calcium carbonate, and the like, and glass beads mixed therein. Have been. In addition, glass beads are generally mixed in an amount of about 15 to 18% by weight with respect to the entire coating material, protrude from the surface of the coating film applied on the road surface, and use the retroreflectivity to enhance the visibility at night. However, in such a conventional hot-melt road marking paint, the amount of glass beads mixed is as low as 15 to 18% by weight. As a result, there is almost no glass beads protruding from the surface of the coating film, resulting in a problem that nighttime visibility is remarkably reduced. In addition, paints are simply blended with binder resin, pigments, fillers, etc., and are not particularly abrasion-resistant, so that on roads with heavy traffic, the wear of the paint film progresses quickly, and the above-mentioned nighttime visibility is high. There is a problem that the property cannot be maintained for a long time. [0004] It is an object of the present invention to provide a heat melting type road marking paint which has solved the above-mentioned conventional problems. SUMMARY OF THE INVENTION In order to solve the above-mentioned problems, the present invention relates to a conventional heat-melting type road marking paint, which is used for a polystyrene-polyisoprene block copolymer resin or a polystyrene-polybutadiene block copolymer resin. By mixing a predetermined amount of these mixed resins or the adhesive resin of the amorphous polyalphaolefin resin, the adhesion between the materials of the coating material is increased to impart flexibility and enhance the impact resistance,
By improving the abrasion resistance and further increasing the amount of glass beads mixed, the visibility at night, in particular, the visibility at the time of wear is improved. That is, the hot-melt road marking paint of the present invention is a hot-melt road marking paint comprising a binder resin, a pigment, a filler, etc.
20% by weight, the adhesive resin is blended in an amount of 1 to 15% by weight based on the whole paint, and the glass beads are mixed in an amount of 30 to 60% by weight based on the whole paint. It is a polystyrene-polyisoprene block copolymer resin, a polystyrene-polybutadiene block copolymer resin, a mixed resin thereof, or an amorphous polyalphaolefin resin. As the binder resin to be blended in the present invention, conventional ones may be used. Generally, a petroleum resin is used, but a thermoplastic resin such as raw rosin, maleated rosin, maleated rosin ester, polyamide resin, unsaturated polyester resin, xylene resin and the like may be used. The compounding ratio of the binder resin is 10 to 2 with respect to the whole paint.
0% by weight. When the content is less than 10% by weight, the fluidity and adhesiveness of the paint are inferior. When the content is more than 20% by weight, the stain resistance of the coating film is poor. Conventional pigments such as white pigments such as titanium dioxide, zinc white and lithopone, and yellow pigments such as graphite and titanium yellow are used as the pigment. The mixing ratio of the pigment is preferably from 2 to 10% by weight based on the whole paint. If the compounding ratio is less than 2% by weight, the coloring power and the hiding power are small, and
If the amount is more than 2% by weight, the effect is not improved any more and only the cost is increased. As the filler, calcium carbonate, silica sand,
Conventional general-purpose materials such as cold water sand and talc are used. The compounding ratio of the filler is preferably from 30 to 50% by weight based on the whole paint. When the compounding ratio is less than 30% by weight, the stain resistance and abrasion resistance of the coating film are inferior. The pressure-sensitive adhesive resin blended in the present invention is used for improving the adhesion between coating materials by the adhesive force, imparting flexibility to the coating film, and improving impact resistance. A styrene-based block copolymer resin composed of a polystyrene-polyisoprene block copolymer resin, a polystyrene-polybutadiene block copolymer resin, or a mixed resin thereof, or an amorphous polyalphaolefin resin is preferably used. The styrene block copolymer resin of the polystyrene-polyisoprene block copolymer resin and the polystyrene-polybutadiene block copolymer resin is a thermoplastic elastomer having an adhesive property and a low melt viscosity. Since the melt viscosity is low, the workability of the paint by the hot melt method is good, and there is an advantage that the softening point of the paint can be maintained as it is despite the low melt viscosity. Further, the polystyrene-polyisoprene block copolymer resin and the polystyrene-polybutadiene block copolymer resin may be mixed in an appropriate ratio, and can be suitably used without impairing the above properties. The amorphous polyalphaolefin resin is a resin having a relatively low molecular weight obtained by copolymerizing propylene with ethylene or brene-1. Generally, it can be used alone as a hot-melt adhesive or sealing agent, and has excellent adhesiveness and compatibility with binder resins, especially petroleum resins. To enhance the impact resistance. The compounding ratio of the adhesive resin is preferably 1 to 15% by weight based on the whole coating composition. If the compounding ratio is less than 1% by weight, sufficient abrasion resistance cannot be obtained in the coating film, and if it is more than 15% by weight, the fluidity of the coating material is deteriorated, the workability is poor, and the edge of the coating film is disordered. 1 to 1
5% by weight is preferred. In particular, when the content exceeds 2% by weight, the fluidity gradually deteriorates, the workability decreases, and it is difficult to obtain a good sign, so that the content is preferably 1 to 2% by weight. The amount of glass beads to be mixed is preferably 30 to 60% by weight based on the whole paint. This mixing amount is 30
If it is less than 60% by weight, the reflection brightness at the time of abrasion of the coating film is insufficient and the night visibility is inferior, and if it is more than 60% by weight, the cost is high and the formation of the coating film is hindered. In particular, 40 to 50% by weight is more preferable from the viewpoint of securing a sufficient reflection luminance at the time of abrasion of the coating film and favorable construction and formation of the coating film. Further, as the glass beads, those having a particle diameter of 60 to 710 μm and a refractive index of 1.5 or more are usually used. Particularly, when high-intensity glass beads are used, night visibility is further improved, which is preferable. In the present invention, besides the above, an antioxidant or a wax as an anti-settling agent, or a plasticizer such as a vegetable oil, a vegetable oil-modified alkyd resin, a phthalic acid ester, or the like is added in an appropriate amount as needed. May be done. Embodiments of the present invention will be described below. It consists of binder resin (petroleum resin), pigment (titanium oxide), filler (calcium carbonate), glass beads, and additives (wax, plasticizer). Using paints (No. 1 to No. 3), these paints are each melted at a temperature of about 200 ° C. and uniformly applied on an aluminum plate to form a coating film having a width of 15 cm, a length of 50 cm and a thickness of 2.0 mm. Formed. The surface of the coating film is uniformly abraded for about 1 minute by using a Plasshot TSP60 manufactured by Toshiba Barotini Co., Ltd. with an ascon blast cabinet BA-1 type direct pressure type machine (manufactured by Atsushi Tekko Co., Ltd.). The reflection luminance at arbitrary 10 points was measured by a luminance measuring device between the time and the wet time, and the results are shown in Table 2. In the abrasion test, a resin powder was used as sandblast to reproduce the abrasion caused by the tire, and the abrasion was uniformly performed without destruction of the glass beads. [Table 1] [Table 2] From Tables 1 and 2, it was confirmed that the reflection luminance value after abrasion was sequentially increased as the amount of glass beads mixed increased. Next, in particular, No.
Based on the paint No. 3, the wear resistance of the coating film was examined by blending a polystyrene-polyisoprene block copolymer resin, a polystyrene-polybutadiene block copolymer resin, and an amorphous polyalphaolefin resin with an adhesive resin. It comprises a binder resin (petroleum resin), a pigment (titanium oxide), a filler (calcium carbonate), glass beads, and additives (wax, plasticizer), and a polystyrene-polyisoprene block copolymer resin (SIS). ) (Quintac 3421 manufactured by Zeon Corporation) with four kinds of paints shown in Table 3 (Examples 1 to 3 and Comparative Example 2) and a paint not containing a polystyrene-polyisoprene block copolymer resin (comparative) Using Example 1), each of these paints was melted at a temperature of about 200 ° C., and JIS K 5665 3
The test was carried out according to various kinds of abrasion resistance test methods, and the results (wear loss) are shown in Table 3. [Table 3] It is composed of a binder resin (petroleum resin), a pigment (titanium oxide), a filler (calcium carbonate), glass beads, and additives (wax, plasticizer), and a polystyrene-polybutadiene block copolymer resin (SBS). Four types of paints shown in Table 4 (Examples 4 to 6, Comparative Example 3) in which the amount of (Quintac BL-301 manufactured by Zeon Corporation) was changed.
Table 4 shows the same test results as above using a paint (Comparative Example 1) containing no polystyrene-polybutadiene block copolymer resin. [Table 4] It comprises a binder resin (petroleum resin), a pigment (titanium oxide), a filler (calcium carbonate), glass beads, and additives (wax, plasticizer), and an amorphous polyalphaolefin resin (APAO). (Ube Tack UT2585 manufactured by Ube Lexen Co., Ltd.) The four types of paints shown in Table 5 (Examples 7 to 9 and Comparative Example 4) in which the blending amount was changed, and a paint not containing an amorphous polyalphaolefin resin (Comparative Example 1)
And the test results similar to the above were shown in Table 5. [Table 5] As can be seen from Tables 3 to 5, it was confirmed that the weight loss was large in Comparative Examples 1 to 4 and small in Examples 1 to 9. Also, polystyrene-
In Examples 3, 6, and 9 in which the blending amounts of the polyisoprene block copolymer resin, the polystyrene-polybutadiene block copolymer resin, and the amorphous polyalphaolefin resin were 2% by weight, respectively, In comparison, the fluidity of the paint was slightly lowered, and the surface of the coating film had a little sticky feeling. As described in detail above, the hot-melt road marking paint of the present invention is a polystyrene-polyisoprene block copolymer resin, a polystyrene-polybutadiene block copolymer resin, a mixed resin thereof, or an amorphous poly- ylene resin. Adhesive resin of alpha olefin resin is 1 to the whole paint
-15% by weight, it is possible to improve the abrasion resistance of the coating film formed on the road surface as compared with the related art. Further, glass beads are contained in 30% of the total paint.
6060% by weight, the glass beads are difficult to peel off from the coating film in combination with the above-mentioned adhesive resin, and the night visibility can be improved.
In addition, even if the coating film is slightly peeled off, the visibility at night can be maintained in a good state, and its reflection performance can be maintained over a long period of time.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C09D 5/00 C09D 7/12 ──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int.Cl. 7 , DB name) C09D 5/00 C09D 7/12

Claims (1)

(57)【特許請求の範囲】 【請求項1】 粘結樹脂、顔料、充填剤などからなる加
熱溶融型道路標示塗料において、粘結樹脂は塗料全体に
対して10〜20重量%配合され、粘接着性樹脂が塗料
全体に対して1〜15重量%配合され、ガラスビーズが
塗料全体に対して30〜60重量%混入されてなり、上
記粘接着性樹脂がポリスチレン−ポリイソプレンブロッ
ク共重合樹脂又はポリスチレン−ポレブタジエンブロッ
ク共重合樹脂又はこれらの混合樹脂又は非晶性ポリアル
ファオレフィン樹脂である加熱溶融型道路標示塗料。
(57) [Claim 1] In a hot-melt type road marking paint comprising a binder resin, a pigment, a filler and the like, the binder resin is blended in an amount of 10 to 20% by weight based on the whole paint, The adhesive resin is blended in an amount of 1 to 15% by weight based on the entire coating composition, glass beads are mixed in an amount of 30 to 60% by weight based on the entire coating composition, and the adhesive resin is a polystyrene-polyisoprene block. A heat melting type road marking paint which is a polymer resin, a polystyrene-polybutadiene block copolymer resin, a mixed resin thereof, or an amorphous polyalphaolefin resin.
JP05643194A 1994-03-28 1994-03-28 Heat melting type road marking paint Expired - Lifetime JP3399485B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP05643194A JP3399485B2 (en) 1994-03-28 1994-03-28 Heat melting type road marking paint

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP05643194A JP3399485B2 (en) 1994-03-28 1994-03-28 Heat melting type road marking paint

Publications (2)

Publication Number Publication Date
JPH07258583A JPH07258583A (en) 1995-10-09
JP3399485B2 true JP3399485B2 (en) 2003-04-21

Family

ID=13026910

Family Applications (1)

Application Number Title Priority Date Filing Date
JP05643194A Expired - Lifetime JP3399485B2 (en) 1994-03-28 1994-03-28 Heat melting type road marking paint

Country Status (1)

Country Link
JP (1) JP3399485B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102787568A (en) * 2012-05-18 2012-11-21 武汉理工大学 Method for setting double-row road surface speed control edge lines for controlling vehicle speed

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100826754B1 (en) * 2001-12-21 2008-04-30 삼성토탈 주식회사 Poly ?-olefin resin for extrusion coating or extrusion laminating
KR100914853B1 (en) * 2009-04-21 2009-09-04 홍종일 Thermal adhesion sheet for road surface marking
CN112322136B (en) * 2020-11-20 2021-11-26 天津市公路工程总公司 Efficient retro-reflection hot-melting highway marking and manufacturing method thereof
CN114621622B (en) * 2022-03-10 2022-12-16 华南理工大学 Hot-melt marking line modified material and hot-melt marking line coating
CN115595011B (en) * 2022-11-11 2024-02-02 刘吉光 Hot-melt traffic marking paint and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102787568A (en) * 2012-05-18 2012-11-21 武汉理工大学 Method for setting double-row road surface speed control edge lines for controlling vehicle speed
CN102787568B (en) * 2012-05-18 2015-04-08 武汉理工大学 Method for setting double-row road surface speed control edge lines for controlling vehicle speed

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