JPS63122763A - Coating composition for running surface of track - Google Patents

Coating composition for running surface of track

Info

Publication number
JPS63122763A
JPS63122763A JP26872486A JP26872486A JPS63122763A JP S63122763 A JPS63122763 A JP S63122763A JP 26872486 A JP26872486 A JP 26872486A JP 26872486 A JP26872486 A JP 26872486A JP S63122763 A JPS63122763 A JP S63122763A
Authority
JP
Japan
Prior art keywords
weight
parts
particle size
aggregate
mohs hardness
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.)
Pending
Application number
JP26872486A
Other languages
Japanese (ja)
Inventor
Mitsuaki Misaizu
美齋津 光昭
Uichi Uchida
内田 卯一
Shigeo Mita
三田 繁夫
Kinichiro Yamamoto
山本 金一郎
Tomiyoshi Ikeda
池田 富芳
Katsuyuki Takahashi
克幸 高橋
Shinichi Masuda
真一 増田
Naoyuki Kishi
岸 直行
Akio Kikuchi
菊池 秋雄
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.)
ATOM KAGAKU TORYO KK
LION KIKAKU KOGYO KK
SAITAMA SHINTOSHI KOTSU KK
Railway Technical Research Institute
Original Assignee
ATOM KAGAKU TORYO KK
LION KIKAKU KOGYO KK
SAITAMA SHINTOSHI KOTSU KK
Railway Technical Research Institute
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 ATOM KAGAKU TORYO KK, LION KIKAKU KOGYO KK, SAITAMA SHINTOSHI KOTSU KK, Railway Technical Research Institute filed Critical ATOM KAGAKU TORYO KK
Priority to JP26872486A priority Critical patent/JPS63122763A/en
Publication of JPS63122763A publication Critical patent/JPS63122763A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain the titled composition giving a coating film having excellent abrasion resistance and removability of deposited ice and snow from the film and applicable within a short period in the intervals of operation of trains, by adding three kinds of aggregate having different particle diameter to a binder. CONSTITUTION:The objective composition is produced by compounding (A) 100pts.wt. of acrylic syrup, a thermoplastic polyamide resin or an epoxy-polythiol binder with (B) a mixture of (i) 10-80pts.wt. of aggregate having particle diameter of 0.5-1.0mm and a Mohs hardness of >=6.5, (ii) 50-300pts.wt. of aggregate having particle diameter of 0.2-1.0mm and Mohs hardness of >=6.5 and (iii) 20-150pts.wt. of aggregate having particle diameter of <=0.1mm. A coating of a road surface having high abrasion resistance and excellent removability of deposited ice and snow from the coating can be formed within a short working period by applying the mixture with an applicator capable of controlling the coating thickness of the running surface of a track at a width wider than the width of tire. The composition is useful also for the protection of the rail surface of a new municipal transportation system.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は軌道走行路面被覆用組成物に関するものであり
、更に詳しくは新都市交通中量輸送システム(側方案内
方式)(以下新都市交通という)におけるコンクリート
で構築された軌道走行路面の特にタイヤが通過する走行
路面を保護する目的で塗装する被覆材に関するものであ
る。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a composition for covering a track running surface, and more specifically, the present invention relates to a composition for covering a track running surface, and more specifically, it relates to a composition for coating a track running surface, and more specifically, a new urban transportation medium-volume transportation system (lateral guidance system) (hereinafter referred to as a new urban transportation system). The present invention relates to a covering material that is applied to protect the track surface constructed of concrete, especially the surface on which tires pass.

〔従来の技術〕[Conventional technology]

近年、新都市交通において利用されているタイヤを装着
した車両の案内方式は両側壁案内軌条方式となっている
ために、車両のタイヤがコンクリートで構築された軌道
走行路面の同じ場所を常に通過することによってタイヤ
が通過する走行路面部分のコンクリートのみが摩耗され
掘れてしまう欠点がある。さらに冬期においてコンクリ
ートの表面に氷や雪が付着しやすくその除去が困難であ
り、列車の運行を停止しなければならない障害が度々生
じている。このため従来エポキシ樹脂モルタル等が軌道
走行路面に塗装されていたが、かかる方法では硬化時間
が非常に長く通常の列車を運行しない時間帯で作業する
ことが困難であり現在はとんど使用されていない。
In recent years, the guidance system for vehicles equipped with tires used in new urban transportation systems is a guide rail system on both sides, which means that the vehicle's tires always pass through the same location on the concrete track surface. This has the disadvantage that only the concrete on the road surface where the tires pass is worn out and dug. Furthermore, ice and snow tend to adhere to concrete surfaces during the winter and are difficult to remove, often causing problems that require train service to be stopped. For this reason, epoxy resin mortar, etc., has traditionally been painted on the track running surface, but this method takes a very long time to harden, making it difficult to work during times when regular trains are not in operation, so it is rarely used at present. Not yet.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

そこで本発明は前記のような諸問題を解決すべく工夫開
発されたものであって、本発明者等により、特定の組成
からなる軌道走行路面被覆用組成物を例えば塗llW厚
調整可能なアプリケーターで軌道走行路面にタイヤ巾よ
り大きな巾で施工することにより、耐摩耗性が優れ、氷
や雪の除去が容易であり、しかも列車の運行しない短か
い時間内で作業をすることのできる被覆を達成すること
ができた。
Therefore, the present invention has been devised and developed to solve the above-mentioned problems. By applying this coating to the track running surface in a width larger than the tire width, it is possible to create a coating that has excellent wear resistance, makes it easy to remove ice and snow, and can be worked on during short periods when trains are not in operation. I was able to achieve this.

〔問題点を解決するための手段・作用〕本発明によれば
、アクリルシラツブ、熱可塑性ポリアミド樹脂またはエ
ポキシ−ポリチオール系結合剤100重量部に対して、
粒径0.5〜1゜0mmでモース硬度6.5以上の骨材
10〜80重量部、粒径0.2〜1.0市でモース硬度
6.5以上の骨材50〜300重量部、および粒径0゜
1mm以下の骨材20〜150重量部を混合した混合物
よりなる軌道走行路面被覆用組成物によって、前記の問
題点が解決された。
[Means/effects for solving the problem] According to the present invention, for 100 parts by weight of acrylic silub, thermoplastic polyamide resin or epoxy-polythiol binder,
10 to 80 parts by weight of aggregate with a particle size of 0.5 to 1.0 mm and a Mohs hardness of 6.5 or more; 50 to 300 parts by weight of aggregate with a particle size of 0.2 to 1.0 mm and a Mohs hardness of 6.5 or more The above-mentioned problems have been solved by a composition for coating a track running surface comprising a mixture of:

本発明の軌道走行路面被覆用組成物において使用される
アクリルシラツブとしては、 (メタ)アクリル酸モノ
マーあるいはその他のビニル系モノマーの混合物にポリ
マーまたはオリゴマーのアクリル樹脂を混合して成るシ
ロップ状の樹脂および熱可塑性ポリアミド樹脂結合剤と
してはダイマー酸ベースで200℃での溶融粘度が3〜
80ポイズ、軟化点が90〜160℃のものが挙げられ
る。これらの結合剤はその樹脂自体耐摩耗性が優れてお
り、しかも硬化が速かに行われる特徴を有している。ま
たエポキシ−ポリチオール系結合剤も価格的に稍難点が
あるが、硬化速度が大きく本発明の組成物に好ましいも
のである。
The acrylic resin used in the track running road surface coating composition of the present invention is a syrup-like resin made by mixing a polymer or oligomeric acrylic resin with a mixture of (meth)acrylic acid monomer or other vinyl monomer. And as a thermoplastic polyamide resin binder, it is based on dimer acid and has a melt viscosity of 3 to 3 at 200℃.
Examples include those having a softening point of 80 poise and a softening point of 90 to 160°C. The resin itself of these binders has excellent abrasion resistance and is characterized by rapid curing. Although epoxy-polythiol binders also have some drawbacks in terms of price, they have a high curing rate and are therefore preferable for the composition of the present invention.

本発明の軌道走行路面被覆用組成物において使用される
骨材としては耐摩耗性と耐スリップ性及び塗装作業性の
向上のために、粒径0.5〜1゜0alII+でモース
硬度6.5以上の骨材と粒径0. 2〜1.0mmでモ
ース硬度6.5以上の骨材を使用し、さらに塗装作業性
の向上のために粒径0.1m+11以下の骨材を混合す
る。
The aggregate used in the track running road surface coating composition of the present invention has a particle size of 0.5 to 1°0alII+ and a Mohs hardness of 6.5 in order to improve wear resistance, slip resistance, and painting workability. Aggregates with a particle size of 0. Aggregates with a particle size of 2 to 1.0 mm and a Mohs hardness of 6.5 or more are used, and aggregates with a particle size of 0.1 m+11 or less are mixed to improve painting workability.

ここで粒径が0.5〜1.0關でモース硬度6゜5以上
の骨材の代わりに粒径が0. 2〜0.1mmでモース
硬度6.5以上の骨材にすることは、粒度分布の影響に
より塗膜表面が平滑になり過ぎて氷や雪の除去は容易で
あるが滑りやすく危険であることから本被覆用組成物に
は適さない。さらに同じく粒径が0.5〜1.01でモ
ース硬度6゜5以上の骨材の代わりに、粒径が1.0〜
2. 0mmの骨材に換えた場合は、逆に塗膜表面が荒
くなり過ぎて滑りにくく安全性は高いが、列車走行時の
騒音が大きくなることや、氷や雪の除去が困難になるこ
とから本被覆用組成物には適さない。また粒径が0.2
〜1.0mmでモース硬度6.5以上の骨材の代わりに
粒径が0.5〜1.0mmでモース硬度6.5以上の骨
材を用いた場合も塗装作業性が劣ることから本被覆用組
成物には適さない。
Here, instead of using aggregate with a particle size of 0.5 to 1.0 and a Mohs hardness of 6°5 or more, the particle size is 0.5 to 1.0. Using aggregate with a Mohs hardness of 6.5 or higher with a thickness of 2 to 0.1 mm makes the coating surface too smooth due to the particle size distribution, making it easy to remove ice and snow, but making it slippery and dangerous. Therefore, it is not suitable for this coating composition. Furthermore, instead of the same aggregate with a particle size of 0.5 to 1.01 and a Mohs hardness of 6°5 or more, aggregate with a particle size of 1.0 to 1.01 and a Mohs hardness of 6°5 or more
2. If you change to 0mm aggregate, on the other hand, the coating surface will become too rough, making it less slippery and safer, but it will make more noise when the train is running, and it will be difficult to remove ice and snow. Not suitable for this coating composition. Also, the particle size is 0.2
If aggregate with a particle size of 0.5 to 1.0 mm and a Mohs hardness of 6.5 or more is used instead of aggregate with a Mohs hardness of 6.5 or more and a particle size of ~1.0 mm, the painting workability will be poor, so this book Not suitable for coating compositions.

したがって本発明における被覆用組成物としては、結合
材100重量部に対して粒径が0.5〜1゜0mmでモ
ース硬度6.5以上の骨材10〜80重量部、好ましく
は30〜60の重量部、粒径が0゜2〜1.0mmでモ
ース硬度6.5以上の骨材50〜300重量部、好まし
くは100〜200重量部、および粒径が0.1mm以
下の骨材20〜150重量部、好ましくは50〜100
重量部を含有した被覆用組成物が適している。ここで粒
径が011mm以下の骨材は専ら組成物の流動性および
作業性を向上させるためのものであって、特に硬度を限
定する必要はない。
Therefore, in the coating composition of the present invention, 10 to 80 parts by weight, preferably 30 to 60 parts by weight of aggregate having a particle size of 0.5 to 1.0 mm and a Mohs hardness of 6.5 or more, to 100 parts by weight of the binder. 50 to 300 parts by weight, preferably 100 to 200 parts by weight, of aggregate with a particle size of 0°2 to 1.0 mm and a Mohs hardness of 6.5 or more, and 20 parts by weight of aggregate with a particle size of 0.1 mm or less. ~150 parts by weight, preferably 50-100 parts by weight
Parts by weight of coating compositions are suitable. Here, the aggregate having a particle size of 0.11 mm or less is used solely for improving the fluidity and workability of the composition, and there is no need to particularly limit the hardness.

本発明の軌道走行路面被覆用組成物の路面への塗装方法
としてはアプリケーター塗装、スプレー塗装、コテ塗装
等を適用することができるが、塗装作業を列車の運行し
ない短時間に行なわなければならないこと及び車両タイ
ヤの通過によりできたコンクリートの凹部をなくさなけ
ればならないこと(なぜならば凹部に水が溜まり凍結に
よって列車の運行を停止する事態をまねきやすくなる。
Applicator painting, spray painting, trowel painting, etc. can be applied to the road surface with the track running road surface coating composition of the present invention, but the painting work must be done in a short time when trains are not in operation. and the need to eliminate concavities in the concrete created by the passing of vehicle tires (because water collects in the concavities and can easily freeze, leading to a situation where train operations are halted).

)等の条件を考慮しなければならない。従ってスプレー
塗装の場合は、1回でスプレーする場合凹部がそのまま
残ってしまい、また凹部を残さないようにするには凹部
に多くスプレーしたりするので手間がかかり余り好まし
くない。また、コテ塗装の場合は、1回で仕上げること
ができない他、コテ目ができたり凹部が残ったりするの
で余り好ましくない。最後に、アプリケーター塗装の場
合は、塗装機を押す或は引くという簡単な操作で短時間
で作業できる他、全体として平面状に仕上げることがで
きるという特徴があり、アプリケーター塗装が好ましい
。さらに、本発明の被覆用組成物において用いる骨材の
粒径の関係から塗膜厚が1゜0〜4.0m+w、好まし
くは1.5〜3.0mm、になるように調整されたアプ
リケーターで塗装するのが好ましい。
) and other conditions must be considered. Therefore, in the case of spray painting, if one spray is applied, the recesses remain as they are, and in order to avoid leaving recesses, a large amount of spray must be applied to the recesses, which is very time-consuming and undesirable. Further, in the case of painting with a trowel, it is not preferable because it is not possible to finish in one step and also leaves trowel marks and recesses. Finally, in the case of applicator painting, it is possible to work in a short time by simply pushing or pulling the atomizer, and it is also possible to finish the entire surface in a flat shape, so applicator painting is preferable. Furthermore, in view of the particle size of the aggregate used in the coating composition of the present invention, an applicator adjusted so that the coating film thickness is 1°0 to 4.0 m+w, preferably 1.5 to 3.0 mm. Painting is preferred.

塗膜厚が1.0mm以下の場合は塗装するときに骨材の
粒径の影響で均一な塗膜状態で仕上がらなくなる(スジ
引き、骨材の突起が著しい)ので塗膜表面が荒くなり、
騒音やタイヤの摩耗が著しくなることから好ましくない
。逆に塗膜厚が4.01以上になると被覆材が硬化する
直前に流動したり、塗膜表面が平滑になり車輪が滑り易
くなるので好ましくない。塗膜厚が1.0〜4.0mm
の場合、骨材が適度の突起を形成するので騒音およびタ
イヤの著しい摩耗がなく、また車輪が滑りにくく好まし
い塗膜が得られる。
If the coating thickness is less than 1.0 mm, the coating will not be finished in a uniform state due to the particle size of the aggregate (streaking and protrusions of the aggregate will be noticeable), and the coating surface will become rough.
This is undesirable because it increases noise and tire wear. On the other hand, if the coating thickness is 4.01 or more, it is not preferable because the coating material may flow just before it hardens or the coating surface may become smooth and the wheels may easily slip. Coating film thickness is 1.0-4.0mm
In this case, the aggregate forms appropriate protrusions, so there is no noise and significant tire wear, and a desirable coating film is obtained that prevents the wheels from slipping.

また、塗装の際に結合材にアクリルシラツブを使用した
場合は、塗装の直前に硬化剤として過酸化ベンゾイル<
ta度50重四%)を1重量%〜3重世%混合撹拌して
用いる。また結合材に熱可塑性ポリアミド樹脂を使用し
た場合は約200℃に加熱溶融して用いる。
In addition, if acrylic silub is used as a binding material during painting, benzoyl peroxide is used as a hardening agent just before painting.
50% by weight) is used by mixing and stirring 1% to 3% by weight. When thermoplastic polyamide resin is used as the binder, it is heated and melted at about 200°C.

以下の実施例および比較例によって本発明を更に具体的
に説明する。
The present invention will be explained in more detail with reference to the following examples and comparative examples.

実施例1 アクリルシラツブ(三菱レイヨン(株)製、商品名:ア
クリルシラツブDR−460): 100重量部粒径0
.5〜1.0mmでモース硬度7.5のセラ9218粒
        =20重世部粒径0.2〜1.0mm
でモース硬度7の珪砂5号           :1
70重量部粒径0.1+m以下の炭酸カルシウム:  
60m1t部の混合物に過酸化ベンゾイル(tffi度
50重景%重量2重量%混合撹拌して被覆用組成物を得
た。
Example 1 Acrylic silub (manufactured by Mitsubishi Rayon Co., Ltd., trade name: acrylic silub DR-460): 100 parts by weight Particle size 0
.. Cera 9218 grains with a Mohs hardness of 7.5 at 5-1.0 mm = 20 grains with a grain size of 0.2-1.0 mm
Silica sand No. 5 with a Mohs hardness of 7: 1
70 parts by weight Calcium carbonate with a particle size of 0.1+m or less:
A coating composition was obtained by mixing and stirring 2% by weight of benzoyl peroxide (TFFI degree 50% by weight) into 60ml/t part of the mixture.

実施例2 アクリルシラツブ(三菱レイヨン(株)製、商品名ニア
クリルシラツブDR−460)  :100重量部粒径
0.5〜1.0IIIolでモース硬度7.5のセラ9
218粒        :40重量部粒径0,2〜1
.0neII+でモース硬度7の珪砂5号      
     =130重量部粒径0.1mm以下の炭酸カ
ルシウム ニア0重量部の混合物に過酸化ベンゾイル(
:a度50重量%)を2重量%混合撹拌して被覆用組成
物を得た。
Example 2 Acrylic silub (manufactured by Mitsubishi Rayon Co., Ltd., trade name Niacrylic silub DR-460): 100 parts by weight Cera 9 with a particle size of 0.5 to 1.0 IIIol and a Mohs hardness of 7.5
218 grains: 40 parts by weight Particle size 0.2-1
.. Silica sand No. 5 with 0neII+ and Mohs hardness of 7
= 130 parts by weight Calcium carbonate with a particle size of 0.1 mm or less Add benzoyl peroxide (
: 50% by weight) was mixed and stirred to obtain a coating composition.

実施例3 アクリルシラツブ(三菱レイヨン(株)製、アクリルシ
ラツブDR−460)     : 100重量部粒径
0.5〜1.0mmでモース硬度7.5のセラ9218
粒        ニア0重量部粒径0.2〜1.0m
mでモース硬度7の珪砂5号           ニ
ア0重量部粒径0.in++++以下の炭酸カルシウム
 :80重量部の混合物に過酸化ベンゾイル(濃度50
重量%)を2重量%混合撹拌して被覆用組成物を得た。
Example 3 Acrylic silub (manufactured by Mitsubishi Rayon Co., Ltd., acrylic silub DR-460): 100 parts by weight Cera 9218 with a particle size of 0.5 to 1.0 mm and a Mohs hardness of 7.5
Particles Near 0 parts by weight Particle size 0.2-1.0m
No. 5 silica sand with a Mohs hardness of 7 m, near 0 parts by weight, particle size 0. Calcium carbonate below in++++: 80 parts by weight of benzoyl peroxide (concentration 50
% by weight) were mixed and stirred to obtain a coating composition.

実施例4 熱可塑性ポリアミド樹脂(ヘンケル白水(株)製、パー
サロン113B)         : 100重量部
粒径0.5〜1.0關でモース硬度7.5のセラ921
8粒        ?  20!量部粒径0.2〜1
.0關でモース硬度7の珪砂5号          
 :170重量部粒径0.1mm以下の炭酸カルシウム
 :60重量部を200℃に加熱溶融し、混合撹拌して
被覆用組成物を得た。
Example 4 Thermoplastic polyamide resin (manufactured by Henkel Hakusui Co., Ltd., Persalon 113B): 100 parts by weight Cera 921 with a particle size of 0.5 to 1.0 and a Mohs hardness of 7.5
8 grains? 20! Part particle size 0.2-1
.. Silica sand No. 5 with a Mohs hardness of 7
: 170 parts by weight Calcium carbonate having a particle size of 0.1 mm or less: 60 parts by weight were heated and melted at 200° C., mixed and stirred to obtain a coating composition.

実施例5 熱可塑性ポリアミド樹脂(ヘンケル白水(株)製、パー
サロン113B)         : 100重量部
粒径0.5〜1.0mmでモース硬度7.5のセラ92
18粒        :40重量部粒径0.2〜1.
軸−でモース硬度7の珪砂5号           
=130重量部粒径0.1m+w以下の炭酸カルシウム
 ニア0重量部を200℃に加熱溶融し、混合撹拌して
被覆用組酸物を得た。
Example 5 Thermoplastic polyamide resin (manufactured by Henkel Hakusui Co., Ltd., Persalon 113B): 100 parts by weight Cera 92 with a particle size of 0.5 to 1.0 mm and a Mohs hardness of 7.5
18 grains: 40 parts by weight Particle size 0.2-1.
No. 5 silica sand with a Mohs hardness of 7 on the axis
= 130 parts by weight 0 parts by weight of calcium carbonate having a particle size of 0.1 m+w or less was heated and melted at 200°C, mixed and stirred to obtain a composite acid for coating.

実施例6 熱可塑性ポリアミド樹脂(ヘンケル白水(株)製、パー
サロン1138)         : 100重量部
粒径0.5〜1.0mmでモース硬度7.5のセラ9フ
18粒        :  70fE量部粒径0.2
〜1.0mmでモース硬度7の珪砂5号       
    ニア0重量部粒径0.1順以下の炭酸カルシウ
ム :80重量部を200℃に加熱溶融し、混合撹拌し
て被覆用組成物を得た。
Example 6 Thermoplastic polyamide resin (manufactured by Henkel Hakusui Co., Ltd., Persalon 1138): 100 parts by weight 18 grains of Cera9f with a particle size of 0.5 to 1.0 mm and a Mohs hardness of 7.5: 70 fE parts particle size 0 .2
Silica sand No. 5 with ~1.0 mm and Mohs hardness of 7
Calcium carbonate having a particle diameter of 0.1 or less: 80 parts by weight was heated and melted at 200° C., mixed and stirred to obtain a coating composition.

実施例7 エポキシ樹脂(シェル化学(株)製、 商品名:エピコート828)      :  60重
量部ポリチオール系硬化剤(東洋レイヨン(株)製、商
品名二東しチオコールLP3)   :  40重量部
アミン系触媒(シェル化学(株)、 商品名:DMP30)         :  0.2
重量部粒径0.5〜1.Ommでモース硬度7.5のセ
ラ9フ18粒        :  40jtit部粒
径0.2〜1.0mmでモース硬度7の珪砂5号   
        :130重量部粒径0.1mm以下の
炭酸カルシウム ニア0重量部を混合撹拌して被覆用組
成物を得た。
Example 7 Epoxy resin (manufactured by Shell Kagaku Co., Ltd., trade name: Epicote 828): 60 parts by weight Polythiol curing agent (manufactured by Toyo Rayon Co., Ltd., trade name Nito Shithiokol LP3): 40 parts by weight Amine catalyst (Shell Chemical Co., Ltd., product name: DMP30): 0.2
Particle size in parts by weight: 0.5-1. 18 grains of Sera 9 with a Mohs hardness of 7.5 in Omm: Silica sand No. 5 with a grain size of 0.2 to 1.0 mm and a Mohs hardness of 7 in the 40jtit section
: 130 parts by weight 0 parts by weight of calcium carbonate having a particle size of 0.1 mm or less were mixed and stirred to obtain a coating composition.

比較例1 アクリルシラツブ(三菱レイヨン(株)製、アクリルシ
ラツブDR−460)     : 100重量部粒径
0.2”l、0LIIr@でモース硬度7の珪砂5号 
          :170重量部粒径0. llm
−以下の炭酸カルシウム =70重量部の混合物に過酸
化ベンゾイル(濃度50重量%)を2重量%混合撹拌し
て混合物を得た。
Comparative Example 1 Acrylic Silica Rubber (manufactured by Mitsubishi Rayon Co., Ltd., Acrylic Silica Rubber DR-460): 100 parts by weight Silica sand No. 5 with a particle size of 0.2”l, 0LIIr@ and a Mohs hardness of 7
: 170 parts by weight Particle size 0. llm
- 2% by weight of benzoyl peroxide (concentration: 50% by weight) was mixed and stirred into a mixture of 70 parts by weight of the following calcium carbonate to obtain a mixture.

比較例2 アクリルシラツブ(三菱レイヨン(株)製、アクリルシ
ラツブDR−460)     : 100重量部粒径
0.5〜1 、0mmでモース硬度7.5のセラ9フ1
8粒        :100重量部粒径0.2〜1 
、 Omn+でモース硬度7の珪砂5号       
    :40重量部粒径0.1mm以下の炭酸カルシ
ウム ニア0重量部の混合物に過酸化ベンゾイル(濃度
50重量%)を2重量%混合撹拌して混合物を得た。
Comparative example 2 Acrylic silub (manufactured by Mitsubishi Rayon Co., Ltd., acrylic silub DR-460): 100 parts by weight Cera 9 F1 with a particle size of 0.5 to 1 and a Mohs hardness of 7.5 at 0 mm
8 grains: 100 parts by weight Particle size 0.2-1
, No. 5 silica sand with Mohs hardness of 7 in Omn+
: 40 parts by weight A mixture of 0 parts by weight of calcium carbonate having a particle size of 0.1 mm or less was mixed with 2% by weight of benzoyl peroxide (concentration 50% by weight) and stirred to obtain a mixture.

比較例3 アクリルシラツブ(三菱レイヨン(株)製、アクリルシ
ラツブDR−460)     7100!量部粒径0
.5〜1.0mmでモース硬度7.5のセラ9フ18粒
        =20重量部粒径0.2〜1.0開で
モース硬度7の珪砂5号           :25
0重量部粒径0.1mm以下の炭酸カルシウム :10
重量部の混合物に過酸化ベンゾイル(tffi度50度
量0重量%重量%混合撹拌して混合物を得た。
Comparative example 3 Acrylic silub (manufactured by Mitsubishi Rayon Co., Ltd., acrylic silub DR-460) 7100! Weight part particle size 0
.. 18 grains of Sera9 with a grain size of 5 to 1.0 mm and a Mohs hardness of 7.5 = 20 parts by weight Silica sand No. 5 with a grain size of 0.2 to 1.0 mm and a Mohs hardness of 7: 25
0 parts by weight Calcium carbonate with a particle size of 0.1 mm or less: 10
A mixture of benzoyl peroxide (tffi degree: 50 degrees: 0% by weight) was mixed and stirred into a mixture of parts by weight to obtain a mixture.

比較例4 アクリルシラツブ(三菱レイヨン(株)製、アクリルシ
ラツブDR−460)     : 100重量部粒径
1.0〜2.0mmでモース硬度7.5のセラサ7ドA
粒        :  40!lli部粒径0.2〜
1 、 On+nでモース硬度7の珪砂5号     
      :130重量部粒径0.1關以下の炭酸カ
ルシウム ニア070重量混合物に過酸化ベンゾイル(
濃度50重量%)を2重量%混合撹拌して混合物を得た
Comparative example 4 Acrylic silub (manufactured by Mitsubishi Rayon Co., Ltd., acrylic silub DR-460): 100 parts by weight Cerasa 7 de A with a particle size of 1.0 to 2.0 mm and a Mohs hardness of 7.5
Grains: 40! lli part particle size 0.2~
1. Silica sand No. 5 with a Mohs hardness of 7 on + n
: 130 parts by weight Calcium carbonate with a particle size of 0.1 or less
(Concentration: 50% by weight) was mixed and stirred to obtain a mixture.

比較例5 アクリルシラツブ(三菱レイヨン(株)製、アクリルシ
ラツブDR−460)     : 100重量部粒径
0.5〜1 、0mmでモース硬度7.5のセラ9フ1
8粒        :4o重量部粒径0.2〜1.0
關でモース硬度3の炭酸カルシウム        :
130重量部粒径0.1m!I以下の炭酸カルシウム 
ニア0重量部の混合物に過酸化ベンゾイル(濃度50重
量%)を2重量%混合撹拌して混合物を得た。
Comparative example 5 Acrylic silub (manufactured by Mitsubishi Rayon Co., Ltd., acrylic silub DR-460): 100 parts by weight Cera 9 F1 with a particle size of 0.5 to 1 and a Mohs hardness of 7.5 at 0 mm
8 grains: 4o parts by weight particle size 0.2-1.0
Calcium carbonate with a Mohs hardness of 3:
130 parts by weight Particle size 0.1m! Calcium carbonate below I
2% by weight of benzoyl peroxide (concentration 50% by weight) was mixed and stirred into 0 parts by weight of the mixture to obtain a mixture.

比較例6 従来使用されているエポキシ樹脂モルタルの例:エポキ
シ樹脂(シェル化学(株)製、 エピコート82B)        ニア0重置部アミ
ン硬化剤CACR社製、へCRハードナー)13219
)=30重量部 珪砂5号、6号、7号の混合物  :600重量部を混
合して混合物を得た。
Comparative Example 6 Examples of conventionally used epoxy resin mortar: Epoxy resin (manufactured by Shell Chemical Co., Ltd., Epicoat 82B) Near 0 overlapped part amine hardener (manufactured by CACR Corporation, HeCR Hardener) 13219
) = 30 parts by weight Mixture of silica sand Nos. 5, 6, and 7: 600 parts by weight were mixed to obtain a mixture.

比較例7 市販セメント1:砂2のモルタルを調製し、そのまま以
下の試験に供した。
Comparative Example 7 A mortar of commercially available cement 1:sand 2 was prepared and subjected to the following test as it was.

以上の実施例および比較例で得た組成物および混合物を
次のように比較試験した。
The compositions and mixtures obtained in the above Examples and Comparative Examples were comparatively tested as follows.

比較試験−1 実施例!−7の組成物及び比較例1−4の混合物を用い
てアプリケーターで塗装したときの作業性と塗膜の表面
状態の確認試験を行なった。
Comparative test-1 Example! Using the composition of Comparative Example 1-7 and the mixture of Comparative Example 1-4, a test was conducted to confirm the workability and surface condition of the coating film when applied with an applicator.

試験結果は第1表の通りである。The test results are shown in Table 1.

試験方法: 作業性は内径57mmの円筒の円錐形底部に内径9mm
の穴の開いた容器に被覆用組成物を満たし、200gの
組成物が下方の容器に落下するのに要した時間をストッ
プウォッチで測定した。ただしこの円筒状の容器は温度
調整ができるものを使用し、実施例1〜3と実施例7の
組成物及び比較例1〜4の混合物は室温20℃で、実施
例4〜6の組成物は200℃に加熱溶池してそれぞれ円
筒状の容器を約20℃及び200℃に温度調整して測定
した。
Test method: Workability was determined using a cylinder with an inner diameter of 9 mm at the conical bottom of a cylinder with an inner diameter of 57 mm.
A container with holes was filled with the coating composition, and the time required for 200 g of the composition to fall into the container below was measured using a stopwatch. However, this cylindrical container was one that could be adjusted in temperature, and the compositions of Examples 1 to 3 and Example 7 and the mixtures of Comparative Examples 1 to 4 were kept at room temperature of 20°C, and the compositions of Examples 4 to 6 were kept at room temperature of 20°C. Measurements were made by heating the melt to 200°C and adjusting the temperature of cylindrical containers to approximately 20°C and 200°C, respectively.

塗膜表面の仕上がり状態は塗膜厚2.0mmになるよう
に調整したアプリケーターで塗膜を作製した時の■塗膜
表面の均一性の外観評価(○:良好、X:不可)と■ボ
ータプルのすべり抵抗試験機で湿潤面でのすべり抵抗値
を測定した。
The finished state of the paint film surface was evaluated by ■Appearance evaluation of the uniformity of the paint film surface (○: Good, The slip resistance value on the wet surface was measured using a slip resistance tester.

第1表 注−に作業性は数値の小さいほど良好であり、およそ1
0秒位いまでか実際の作業に適する。
As noted in Table 1, the smaller the number, the better the workability, and approximately 1
Approximately 0 seconds is suitable for actual work.

注−2:すべり抵抗値は数値の大きいほどすべりににく
く、通常の列車走行状態では湿潤面で50以上あれば良
好。
Note-2: The higher the slip resistance value, the less likely it is to slip, and under normal train running conditions, a value of 50 or more on a wet surface is good.

第1表の結果から明らかなように、本発明の軌道走行路
面被覆用組成物によれば、塗装の作業性が良く、仕上が
り状態が均一で適度に耐スリップ性があり、しかも摩耗
量の少ないすぐれた被覆性能を示す塗膜が得られる。
As is clear from the results in Table 1, the composition for coating track running surfaces of the present invention has good coating workability, a uniform finish, moderate slip resistance, and less wear. A coating film exhibiting excellent coating performance is obtained.

これに対し、粒径0. 5〜1.0mmの膏剤を使わな
い場合(比較例1)は耐スリップ性が劣り、逆に多過ぎ
た場合(比較例2)及びさらに大きな粒径の膏剤を使用
した場合(比較例4)はアプリケーターで塗装すると骨
材がひっかかりスジを引いて表面状態が悪くなるので十
分な被覆用組成物の性能が得られない。
On the other hand, the particle size is 0. Slip resistance was poor when a plaster with a particle diameter of 5 to 1.0 mm was not used (Comparative Example 1), whereas when too much was used (Comparative Example 2) and when a plaster with an even larger particle size was used (Comparative Example When applying 4) with an applicator, the aggregate gets caught and causes streaks, resulting in a poor surface condition, making it impossible to obtain sufficient performance of the coating composition.

比較試験−2 実施例1〜7の組成物および比較例5〜7の混合物を用
いて耐摩耗性試験を行った。試験結果は第2表の通りで
ある。
Comparative Test-2 A wear resistance test was conducted using the compositions of Examples 1 to 7 and the mixtures of Comparative Examples 5 to 7. The test results are shown in Table 2.

試験方法: 実施例1〜7の組成物及び比較例5.6の混合物はアル
ミ板上に2.0■の塗膜厚で塗装し、実施例1〜7の組
成物及び比較例5の混合物については1日養生、比較例
6の混合物については1週間養生した後、また、比較例
7は日本テストパネル工業(株)製の厚さ10mmのモ
ルタル板を使用しテーパー摩耗試験を行った。テーパー
摩耗試験は摩耗輪にC3−17を用い荷重1kg、10
0回転での摩耗量を測定した。
Test method: The compositions of Examples 1 to 7 and the mixtures of Comparative Examples 5 and 6 were coated on an aluminum plate with a coating thickness of 2.0 cm. The mixture of Comparative Example 6 was cured for one day, and the mixture of Comparative Example 6 was cured for one week, and the mixture of Comparative Example 7 was subjected to a taper abrasion test using a mortar plate with a thickness of 10 mm manufactured by Nippon Test Panel Industry Co., Ltd. In the taper wear test, C3-17 was used as the wear ring, the load was 1 kg, and 10
The amount of wear at 0 rotations was measured.

第2表 第2表の結果から明らかなように、本発明の軌道走行路
面被覆用組成物は従来の被覆組成物(比較例6)に比べ
て同等以上の耐摩耗性を示した。
As is clear from the results in Table 2, the track running road surface coating composition of the present invention exhibited wear resistance equal to or higher than that of the conventional coating composition (Comparative Example 6).

これに対して粒径0.2mm〜1.0mmでモース硬度
7の珪砂5号をモース硬度3の炭酸カルシウムに換えた
場合(比較例5)は1:2モルタル(比較例7)よりは
摩耗量が少ないが耐摩耗性としては不十分であった。
On the other hand, when silica sand No. 5 with a particle size of 0.2 mm to 1.0 mm and a Mohs hardness of 7 was replaced with calcium carbonate with a Mohs hardness of 3 (Comparative Example 5), the wear was lower than that of the 1:2 mortar (Comparative Example 7). Although the amount was small, the wear resistance was insufficient.

比較試験−3(実路面試験) 実施例2および5の組成物および比較例6の混合物につ
いて埼玉新都市交通・伊奈線の列車引込み線軌道上で気
温5℃の条件で、実施例2および5については各々30
m宛、比較例6は5mの長さで塗装し、下地処理および
硬化時間を含めた施工所要時間と冬期間での氷や雪の除
去性および耐久性について試験した。試験結果は第3表
の通りである。
Comparative Test-3 (Actual Road Surface Test) The compositions of Examples 2 and 5 and the mixture of Comparative Example 6 were tested on the train siding track of Saitama New Urban Transit/Ina Line at a temperature of 5°C. 30 each for
Comparative Example 6 was painted in a length of 5 m and tested for the required construction time including base treatment and curing time, ice and snow removability during winter, and durability. The test results are shown in Table 3.

第3表 第3表の結果から明らかなように、本発明の軌道走行路
面被覆用組成物を使用するときはコンクリートの下地処
理(従来の方法と同様なレイタンスの除去及びプライマ
ーの塗布)及び硬化時間を含めた施工所要時間が大巾に
短かくなった。
Table 3 As is clear from the results in Table 3, when using the track running road surface coating composition of the present invention, concrete surface treatment (removal of laitance and application of a primer similar to the conventional method) and curing are required. The time required for construction, including construction time, has been significantly shortened.

これに対し、従来品(比較例5)は気温が5℃と低いた
めに、約8時間(480分)を要した。
On the other hand, the conventional product (Comparative Example 5) required about 8 hours (480 minutes) because the temperature was as low as 5°C.

〔発明の効果〕〔Effect of the invention〕

本発明の軌道走行路面被覆用組成物によれば、短い作業
時間で耐摩耗性があり氷や雪の除去の容易な路面被覆を
行うことができて、新都市交通の路面保護に側照的な効
果を奏するものである。
According to the track running road surface coating composition of the present invention, it is possible to coat a road surface with wear resistance and easy removal of ice and snow in a short working time, making it ideal for road surface protection for new urban transportation. This has the following effects.

・イ冑H尾:!i、・Lee H tail:! i,

Claims (1)

【特許請求の範囲】[Claims] アクリルシラップ、熱可塑性ポリアミド樹脂またはエポ
キシ−ポリチオール系結合剤100重量部に対して、粒
径0.5〜1.0mmでモース硬度6.5以上の骨材1
0〜80重量部、粒径0.2〜1.0mmでモース硬度
6.5以上の骨材50〜300重量部、および粒径0.
1mm以下の骨材20〜150重量部を混合した混合物
よりなる軌道走行路面被覆用組成物。
1 part of aggregate with a particle size of 0.5 to 1.0 mm and a Mohs hardness of 6.5 or more per 100 parts by weight of acrylic syrup, thermoplastic polyamide resin, or epoxy-polythiol binder
0 to 80 parts by weight, 50 to 300 parts by weight of aggregate with a particle size of 0.2 to 1.0 mm and a Mohs hardness of 6.5 or more, and a particle size of 0.2 to 1.0 mm.
A composition for covering a track running surface, which is made of a mixture of 20 to 150 parts by weight of aggregates having a diameter of 1 mm or less.
JP26872486A 1986-11-13 1986-11-13 Coating composition for running surface of track Pending JPS63122763A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26872486A JPS63122763A (en) 1986-11-13 1986-11-13 Coating composition for running surface of track

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26872486A JPS63122763A (en) 1986-11-13 1986-11-13 Coating composition for running surface of track

Publications (1)

Publication Number Publication Date
JPS63122763A true JPS63122763A (en) 1988-05-26

Family

ID=17462464

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26872486A Pending JPS63122763A (en) 1986-11-13 1986-11-13 Coating composition for running surface of track

Country Status (1)

Country Link
JP (1) JPS63122763A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012180400A (en) * 2011-02-28 2012-09-20 Sekisui Jushi Co Ltd Hot melt road marking paint
WO2016190223A1 (en) * 2015-05-22 2016-12-01 花王株式会社 Material for waterproof layers

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52134639A (en) * 1976-05-04 1977-11-11 Atomu Kagaku Toriyou Kk Material for road sign
JPS5523137A (en) * 1978-08-07 1980-02-19 Mitsubishi Rayon Co Ltd Road marking or floor coating composition
JPS5632552A (en) * 1979-08-27 1981-04-02 Kanagawaken Preparation of abrasion resistant coating material
JPS58171456A (en) * 1982-03-08 1983-10-08 Dainichi Seika Kogyo Kk Coating composition for road and floor

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52134639A (en) * 1976-05-04 1977-11-11 Atomu Kagaku Toriyou Kk Material for road sign
JPS5523137A (en) * 1978-08-07 1980-02-19 Mitsubishi Rayon Co Ltd Road marking or floor coating composition
JPS5632552A (en) * 1979-08-27 1981-04-02 Kanagawaken Preparation of abrasion resistant coating material
JPS58171456A (en) * 1982-03-08 1983-10-08 Dainichi Seika Kogyo Kk Coating composition for road and floor

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012180400A (en) * 2011-02-28 2012-09-20 Sekisui Jushi Co Ltd Hot melt road marking paint
WO2016190223A1 (en) * 2015-05-22 2016-12-01 花王株式会社 Material for waterproof layers
JP2016217044A (en) * 2015-05-22 2016-12-22 東亜道路工業株式会社 Material for waterproof layer

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