JPH02137755A - Road-repairing material - Google Patents

Road-repairing material

Info

Publication number
JPH02137755A
JPH02137755A JP28779988A JP28779988A JPH02137755A JP H02137755 A JPH02137755 A JP H02137755A JP 28779988 A JP28779988 A JP 28779988A JP 28779988 A JP28779988 A JP 28779988A JP H02137755 A JPH02137755 A JP H02137755A
Authority
JP
Japan
Prior art keywords
weight
cement
emulsion
road
pts
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
JP28779988A
Other languages
Japanese (ja)
Inventor
Toshio Mihara
三原 敏夫
Katsuichi Yokobori
横堀 勝一
Kenkichi Hirano
健吉 平野
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.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo KK
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 Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Priority to JP28779988A priority Critical patent/JPH02137755A/en
Publication of JPH02137755A publication Critical patent/JPH02137755A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Abstract

PURPOSE:To enable the road-repairing material to be improve its durability and conduct the road repairing operation in winter even while the road is wet by using cement, an aqueous emulsion of ethylene-acrylic acid ester-vinyl acetate and calcium aluminate as major components. CONSTITUTION:(A) Cement (various kinds of Portland cement, a mixed cement thereof with blast-furnace slag, (B) an aqueous emulsion of ethylene (10 to 30wt.%)-acrylic ester (40 to 85wt.%)-vinyl acetate (5 to 45wt.%) (glass transition point: higher than -30 deg.C) and (C) calcium aluminate (preferably glassy with a CaO content: 30 to 60wt.%, preferably 38 to 52wt.%) are used, as major components, at 2 to 30 pts.wt., preferably 5 to 20 pts.wt. of component D (based on solid part) and 2 to 50 pts.wt. of component C per 100 pts.wt. of component A.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は道路補修材に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to road repair materials.

〔従来の技術とその課題〕[Conventional technology and its issues]

車の数が増加するにつれ、特に冬季、北陸・東北地区等
ではスパイクタイヤ等により道路が破損し、補修が必髪
な状況にある。この補修には、セメント・砂及びアスフ
ァルトを被検した骨材からなる材料やアスファルトのチ
ップを破損部に充填する方法等が提案されている(例え
ば、特開昭54−70621号公報等)が、性能的に十
分でなく、交通量の激しい道路では耐久性が不十分であ
り、耐久性の良好な材料の開発が望まれていた。
As the number of cars increases, roads in the Hokuriku and Tohoku regions are damaged by spiked tires, especially in the winter, and need to be repaired. For this repair, methods have been proposed in which the damaged area is filled with materials made of aggregates tested with cement, sand, and asphalt, or asphalt chips (for example, Japanese Patent Laid-Open Publication No. 70621/1983). However, the performance is not sufficient and the durability is insufficient for roads with heavy traffic, so there has been a desire to develop a material with good durability.

本発明者らは、道路補修材に係る現状の問題点を解決す
べく検討金型ねた結果、特定の材料を用いることによっ
て、耐久性の良好な道路補修材が得られる知見を得て本
発明を完成するに至った。
The present inventors conducted research on molds to solve the current problems related to road repair materials, and as a result, they obtained the knowledge that road repair materials with good durability can be obtained by using specific materials. The invention was completed.

〔課題を解決する九めの手段〕[Ninth means to solve the problem]

即ち、本発明は、セメント100重量部と、エチレン−
アクリル酸エステル−酢酸ビニルからなるガラス転移温
度が一30℃以下である水性共重合体エマルションを固
形分換算で2〜30重量部及びカルシウムアルミネート
類2〜50重量部を主成分とする道路補修材である。
That is, in the present invention, 100 parts by weight of cement and ethylene-
Road repair whose main components are 2 to 30 parts by weight of an aqueous copolymer emulsion consisting of acrylic acid ester and vinyl acetate with a glass transition temperature of 130°C or lower, calculated as solid content, and 2 to 50 parts by weight of calcium aluminates. It is a material.

以下本発明の詳細な説明する。The present invention will be explained in detail below.

本発明で使用するセメントとしては、普通、早強、超早
強等のポルトランドセメントやこれらに高炉スラグ、プ
ライアックユ又はクリ力等を混合した混合セメント等が
使用される。
As the cement used in the present invention, there are normally used portland cements such as early-early-strength and ultra-early-strength cements, and mixed cements in which these are mixed with blast furnace slag, plyacyu, chestnut, etc.

本発明の水性共重合体エマルション(以下本工マルジョ
ンという)のガラス転移温度(以下Tgという)は−3
0℃以下である。
The glass transition temperature (hereinafter referred to as Tg) of the aqueous copolymer emulsion of the present invention (hereinafter referred to as the present process emulsion) is -3
The temperature is below 0°C.

−とは無定形重合体の各種性質が急変する温度であプ、
この温度以下では重合体の無定形部分の分子セグメント
の運動が凍結されるような温度である。Tgの測定方法
としては、DSC法等の熱分析方法が一般的に用いられ
ている。
− is the temperature at which various properties of the amorphous polymer suddenly change;
Below this temperature, the motion of the molecular segments of the amorphous portion of the polymer is frozen. As a method for measuring Tg, a thermal analysis method such as a DSC method is generally used.

本エマルションのT が−60℃以下というととは、本
エマルジョンを構成する共重合体のTgが一30°C以
下であるということであり、上記方法によりTg!t−
求めることができる。しかし実際的には、ホモポリマー
のTgは既に知られてお9、(例えば丸善(株)発行の
化学便覧等ノ、共重合体のTgは個々の単独モノマーよ
りなるホモポリマーのTgより、次の計算式によって推
定することも可能である。
When the T of this emulsion is -60°C or less, it means that the Tg of the copolymer constituting this emulsion is -30°C or less, and the Tg! t-
You can ask for it. However, in practice, the Tg of a homopolymer is already known (for example, in the Chemical Handbook published by Maruzen Co., Ltd.), and the Tg of a copolymer is calculated from the Tg of a homopolymer made of individual monomers as follows. It is also possible to estimate using the calculation formula.

T   T    T       Tgng    
   gl      g2W1:成分10重量分率。
T T T Tgng
gl g2W1: component 10 weight fraction.

W2;成分2  # W :成分n  # (ここでW1+W2+−・・−+wn= 1 )Tg□
:成分1ホモポリマーのT (上)Tg2=成分2 〃 Tgn:成分nI Tg:成分1.2・・・・・・nよりなる共重合体のT
g (K) 本エマルションのTgが一60℃よりも高いと、道路補
修材(以下補修材という)として十分な柔軟性(可とう
性)が発現されず、下地の動きに追随できないで、ひび
割れや亀裂の原因となるおそれがある。
W2; Component 2 #W: Component n # (Here, W1+W2+-...-+wn=1)Tg□
: T of component 1 homopolymer (Top) Tg2 = component 2 〃 Tgn: component nI Tg: T of copolymer consisting of component 1.2...n
g (K) If the Tg of this emulsion is higher than 160°C, it will not exhibit sufficient flexibility as a road repair material (hereinafter referred to as repair material), and will not be able to follow the movement of the base material, causing cracks. Otherwise, it may cause cracks.

本エマルジョン中のエチレン含有量は10〜30重量%
が好ましい。エチレン含有量が10重量係未満ではエマ
ルジョンの耐アルカリ性が不足し、30重量係ヲ越すと
、エマルション状態が不安定になシ、現実の使用に支障
をきたす恐れがある。
The ethylene content in this emulsion is 10 to 30% by weight
is preferred. If the ethylene content is less than 10% by weight, the emulsion will lack alkali resistance, and if it exceeds 30% by weight, the emulsion will become unstable and may pose a problem in actual use.

また、本エマルション中のアクリル酸エステル(以下エ
ステルという)の含有量は40〜85重量%が好ましい
。エステルの含有量が40重量%未満では、本エマルジ
ョンのTgt−−30°C以下にすることが難しく、8
5重量係?越すと乳化重合が不安定になる恐れがある。
Moreover, the content of acrylic ester (hereinafter referred to as ester) in this emulsion is preferably 40 to 85% by weight. If the ester content is less than 40% by weight, it is difficult to reduce the Tgt of the emulsion to -30°C or less, and the
5 Weight section? If the temperature is exceeded, emulsion polymerization may become unstable.

本発明で使用するエステルは、そのホモポリマーのT 
が−50°C以下のものであり、異体的にはノルマルゾ
ロビルアクリレート(n −FA )、ノルマルブチル
アクリレート(n −BA ) 、へ午シルアクリレー
ト(HA)、2−メトキシエチルアクリレート(c−1
)及び2−エチルヘキシルアクリレ−) (2EHA 
)等が一般的に使用できる。
The ester used in the present invention is a homopolymer of T
is -50°C or less, and the isomers include normal zolobyl acrylate (n-FA), normal butyl acrylate (n-BA), hemosil acrylate (HA), and 2-methoxyethyl acrylate (c- 1
) and 2-ethylhexyl acrylate) (2EHA
) etc. can be generally used.

本発明で使用する酢酸ビニル(以下酢ビという)は特に
限定されるものではない。
Vinyl acetate (hereinafter referred to as vinyl acetate) used in the present invention is not particularly limited.

本エマルジョン中の酢ビ含有量は5〜45重量係が好ま
しい。5iitチ未満では、エチレン−酢ビ系共重合体
エマルションの特徴の一つであるセメントとの混和性の
良さが11なわれ、45重量%ヲ越すと、本エマルジョ
ンのTgt−−30℃以下にすることが難しくなる。
The vinyl acetate content in this emulsion is preferably 5 to 45% by weight. If it is less than 5iit, the good miscibility with cement, which is one of the characteristics of the ethylene-vinyl acetate copolymer emulsion, will be lost, and if it exceeds 45% by weight, the Tgt of the emulsion will drop to -30℃ or less. becomes difficult to do.

本エマルジョンの製造方法については特に制限はなく、
乳化重合方法は公知のブ法を便用することができる。ま
た、重合条件にも竹に制限はないが、一般的には重合温
度は20〜80°Cである。
There are no particular restrictions on the manufacturing method of this emulsion.
As the emulsion polymerization method, the well-known B method can be conveniently used. Furthermore, there are no restrictions on the polymerization conditions for bamboo, but generally the polymerization temperature is 20 to 80°C.

触媒としては、過1流酸カリウム等の過硫酸塩、過酸化
水素及び各イ」有機過酸化物等が挙げられる。
Examples of the catalyst include persulfates such as potassium persulfate, hydrogen peroxide, and organic peroxides.

レドックス開始系の場合は、さらに還元性物質としてホ
ルムアルデヒドナトリウムスルホキクレートなどが組み
合せて用いられる。
In the case of a redox initiation system, a reducing substance such as formaldehyde sodium sulfocylate is further used in combination.

乳化剤としては、ポリビニルアルコール、ヒドロ中ジエ
チルセルロース、メチルセルロース等の保膿コロイド、
ポリオキクエチレン縮合体、ポリオキクエチレンポリオ
キクゾロビレンブロックコボリマー等の非イオン性界面
活性剤、アルキルベンゼンスルホ7tlR塩やラウリル
硫酸エステル塩等のアニオン性界面活性剤等が挙げられ
、これらを単独で便用することも、併用することも可能
である。
Emulsifiers include polyvinyl alcohol, diethylcellulose in hydrochloride, methylcellulose, and other purulent colloids;
Examples include nonionic surfactants such as polyoxyethylene condensates and polyoxyethylene polyoxycyclopylene block copolymers, and anionic surfactants such as alkylbenzene sulfo 7tlR salts and lauryl sulfate salts. It can be used conveniently or in combination.

乳化剤の使用量は、通常全モノマー量の2〜10重量幅
である。
The amount of emulsifier used is usually 2 to 10% by weight of the total monomer amount.

本エマルジョンには、さらに必要に応じ、公知の一調整
剤(バッファー)、消泡剤及び防腐剤等の添加剤の使用
が5J能である。
This emulsion may further contain known additives such as buffers, antifoaming agents, and preservatives, if necessary.

本エマルションの使用値は、セメント100重葉部に対
し固形分換算で2〜30重量部である。
The usage value of this emulsion is 2 to 30 parts by weight in terms of solid content per 100 parts of cement.

5〜20重量部が特に好゛ましい。2重量部未満では補
修材の柔軟性が不足し、60重量部を越えると圧縮強度
の低下が著しい。
Particularly preferred is 5 to 20 parts by weight. If it is less than 2 parts by weight, the repair material will lack flexibility, and if it exceeds 60 parts by weight, the compressive strength will be significantly reduced.

本発明で用いるカルシウムアルミネート類(以下CA類
という)としては、通常、電気炉もしくはロータリー中
ルン等によυ高温で生成するカルシウムアルミネート鉱
物?いい、結晶質のもの又はガラス質のものを問わず使
用可能であり、これらの生成過程での他成分や不純物の
存在も特に限定されるものではない。
Calcium aluminates (hereinafter referred to as CAs) used in the present invention are usually calcium aluminate minerals produced at high temperatures in an electric furnace or rotary chamber. Either crystalline or vitreous materials can be used, and the presence of other components and impurities during the production process is not particularly limited.

結晶質のカルシウムアルミネート鉱物としては、CaO
kc、 Al2O3t”AlF3203 kFs Ca
804をC8及びハo )y’ 7 f Xとすると、
CA 、  C5A3、(42A、及びC3A等と示さ
れるもの、並びに、他成分が結晶中に存在する結晶質と
してc、A7CaX2、C3A5(jlX2、C4AF
及びc3A3cs等と示されるもの等があげられる。
As a crystalline calcium aluminate mineral, CaO
kc, Al2O3t”AlF3203 kFs Ca
If 804 is C8 and Hao)y'7fX,
Those indicated as CA, C5A3, (42A, and C3A, etc.), as well as crystalline substances in which other components are present in the crystal, such as c, A7CaX2, C3A5 (jlX2, C4AF
and c3A3cs.

ガラス質のものの代表的カルシウムアルミネート鉱物と
しては、組成物には結晶質のものと同一であるが、急冷
によりガラス化したものであシ、X線的にはそのままで
は特定できない。
Typical glassy calcium aluminate minerals have the same composition as crystalline minerals, but they are vitrified by rapid cooling and cannot be identified by X-rays.

反応性の面からは、結晶質のものよりガラス質のものが
好ましく、組成の面からは、カルシウムアルミネート中
のCaOの含有量が30〜600〜60重量部好ましく
、38〜528〜52重量部特に好ましい。
From the viewpoint of reactivity, glassy ones are preferable to crystalline ones, and from the viewpoint of composition, the content of CaO in calcium aluminate is preferably 30 to 600 to 60 parts by weight, and 38 to 528 to 52 parts by weight. Particularly preferred.

本発明では、以上のようなCA類を一種又は二種以上!
用できる。
In the present invention, one or more of the above CAs are used!
Can be used.

CA類の便用iはセメン)10011L量部に対して、
2〜50重責部である。2〜50fi量部以外では急結
性、作業性、強度及び経済性の点で好ましくない。
Convenient i of CA type is cement) for 10011L parts,
There are 2 to 50 departments with heavy responsibility. Amounts other than 2 to 50 fi parts are unfavorable in terms of rapid setting, workability, strength, and economy.

ま九本発明ではこの他に凝結調節剤、無機硫酸塩等の無
機物質、珪砂や天然砂等の骨材及びガラス繊維や鋼繊維
等の繊維質物質等を併用することもできる。
Additionally, in the present invention, a setting regulator, an inorganic substance such as an inorganic sulfate, an aggregate such as silica sand or natural sand, and a fibrous substance such as glass fiber or steel fiber can also be used in combination.

無機物質としては、特に無機硫酸塩の便用が好ましい。As the inorganic substance, inorganic sulfates are particularly preferred.

需礪1流酸塩とは、アルカリ金属又はアルカリ土類金属
の1訛岐塩tいう。例えば、無水、手水並びに二本の硫
酸カルシウムが好ましいものとして埜げられ、その中で
も、旧型無水石膏のような難溶性又は不溶性のものが躯
に好ましいものとじ−C挙けられる。
The term sulfuric acid salt refers to an alkali metal or alkaline earth metal salt. For example, anhydrous, chozu, and two types of calcium sulfate are preferred, and among these, poorly soluble or insoluble ones such as old-style anhydrite are preferred.

CA類と無機硫酸塩の使用量はCA類100重量部に対
し、50〜500重慧部が好ましく、100〜300重
索部が特に好ましい。
The amount of CAs and inorganic sulfates used is preferably 50 to 500 parts by weight, particularly preferably 100 to 300 parts by weight, per 100 parts by weight of CAs.

本発明の補修材は、各々の材料?施工時に混合してもよ
いし、あらかじめ一部若しくは本エマルジョン以外の材
料全部を混合しておいてもさしつかえない。
Is the repair material of the present invention different from each other? It may be mixed at the time of construction, or some or all of the materials other than the present emulsion may be mixed in advance.

混合には、公知の攪拌装置がいずれも使用可能である。Any known stirring device can be used for mixing.

例えば、傾胴ミキサー オムニミキサーV型ミキサー、
ヘンシエルミ午す− ナウターミキサ−及びボールミル
等が利用できる。
For example, tilting mixer omnimixer V-type mixer,
Hensielmi mixer, Nauta mixer, ball mill, etc. can be used.

ま九、補修材は、一般に行われている左官♂テ、刷毛又
は吹付等で容易に施工可能である。
Also, the repair material can be easily applied using commonly used methods such as plastering, brushing, or spraying.

〔実施例〕〔Example〕

以下、実施例によシ本発明の詳細な説明する。 Hereinafter, the present invention will be explained in detail by way of examples.

実施例1 内容積101のステンレス製電磁攪拌機付オートクレー
ブに、純水、酢ビ、ニスデル及び乳化剤を表1のように
仕込み、内温を70°Cまで上げて、エチレンt60に
9/cIrL2になるまで導入した。触媒として過硼酸
アンモニウム0.6 g?添加し重合を開始した。内温
はジャケットの温度を調整して一定に保った。10時間
後冷却し内容物を取り出したところ、内容物は粗粒の少
ない安定なエマルショ/であった。エマルションのポリ
マー組成などの性状を表−1に示す。
Example 1 Pure water, vinyl acetate, Nisdel and emulsifier were charged as shown in Table 1 into a stainless steel autoclave with an internal volume of 101 cm and equipped with an electromagnetic stirrer, and the internal temperature was raised to 70°C to give ethylene t60 to 9/cIrL2. has been introduced. 0.6 g of ammonium perborate as a catalyst? was added to start polymerization. The internal temperature was kept constant by adjusting the jacket temperature. After cooling for 10 hours, the contents were taken out and found to be a stable emulsion with few coarse particles. Table 1 shows the properties of the emulsion, including its polymer composition.

なお粘度は、BM型回転粘度計を使用し、60°Os 
30 rpmで測定した。
The viscosity was measured at 60°Os using a BM type rotational viscometer.
Measured at 30 rpm.

次に上記のようにJ!!遺し九本エマルションに、セメ
ント、CA類、無機物質入°び骨材を表2の割合で混合
しく5°Cの雰囲気丁)、硬化体全作成し表2に示す性
能評価を行なった。
Next, as mentioned above, J! ! Cement, CA, inorganic substances, and aggregate were mixed into the emulsion in the proportions shown in Table 2 (in an atmosphere of 5°C), and the entire hardened product was prepared and the performance evaluation shown in Table 2 was performed.

(便用材料) エチレン二市販品 AE−a  ニアクリル酸エステルn−13A %三菱
油化裂〃−b:l2EIXA11 気 酢 ピ :酢酸ビニル、電化化学工業具P’/A  :
ポリビニルアルコール、電気化学工業製、商品名[B−
05J 界面剤:商品名[エマルデン931J、花王製HEC:
ヒドロキシエチルセルロース、フジ化学工業製 Na0Aa :酢酸ナトリウム、試薬特級過硫アン:過
硫酸アンモニウム、試薬特級セメント:アンデスセメン
ト社製、普通ポルトランドセメント CA類; CaO45重量%、ガラス質、プレーン比表
面積6,500 cm2/ 11 無機物質−〇:■型無水石膏、プレーン比表面積6.1
0012/ N #   −(L:凝結調節剤、電気化学工業製、商品名
「コスミック、=M 1セツタ ー」 骨 材 :けい砂7号 得られた硬化体の物性は、下記の方法で測定した。但し
、養生及び測定は、5℃X 65 % RHの条件下で
行なつ九。
(Toilet materials) Ethylene 2 commercial product AE-a Niacrylic acid ester n-13A %Mitsubishi Yukasaku-b: 12EIXA11 Air vinegar Pi: Vinyl acetate, Denka Kagaku Kogyo P'/A:
Polyvinyl alcohol, manufactured by Denki Kagaku Kogyo, trade name [B-
05J Surfactant: Product name [Emulden 931J, Kao HEC:
Hydroxyethyl cellulose, manufactured by Fuji Chemical Industry Na0Aa: Sodium acetate, reagent special grade ammonium persulfate: Ammonium persulfate, reagent special grade cement: Manufactured by Andes Cement Co., Ltd., ordinary Portland cement CA class; CaO 45% by weight, vitreous, plain specific surface area 6,500 cm2 / 11 Inorganic substance - 〇: ■ type anhydrite, plain specific surface area 6.1
0012/N#-(L: Setting regulator, manufactured by Denki Kagaku Kogyo, trade name "Cosmic, = M 1 Setter") Aggregate: Silica sand No. 7 The physical properties of the obtained hardened body were measured by the following method. However, curing and measurements were performed under conditions of 5°C and 65% RH.

(a)  ハンドリングタイム(HT )ミキサーで全
材料?混含後、500IJの容器(ビーカー)に入れ、
横にしても流れなくなる時間(流動性がなくなる時間)
tもってHTとした。
(a) Handling time (HT) All materials in mixer? After mixing, put it in a 500 IJ container (beaker),
Time when it stops flowing even when laid down (time when fluidity disappears)
t was used as HT.

(+))  圧縮強度 JI8 R5201に準じた。但し、材令は1時間、6
時間、1日、28日とした。
(+)) Compressive strength According to JI8 R5201. However, the material period is 1 hour, 6
The time was set as 1st and 28th.

(C)  曲げ@戻 、TI8 R5201に蟲じた。但し、材令は28日と
した。
(C) Bending @ return, TI8 R5201 was damaged. However, the material order was set on the 28th.

表2より、適量のCA類の添加によって、初期強度の発
現が早くなり、通量の本エマルジョンの添加によって硬
化体に柔軟性が付与されることが判る。実!%1612
は、CA類及び本エマルジョン無添加の場合であり、強
度発現が遅く、硬化体の柔軟性も低い。実験ム16は、
本エマルジョン無添加の場合であシ、硬化体の柔軟性が
低い。試験慮14はエマルジョンを過剰に添加した場合
であり、硬化体の強度が非常に低下する。実験/161
6は、CA類を過剰に添加した場合であり、硬化体の柔
軟性が低下する。
From Table 2, it can be seen that by adding an appropriate amount of CAs, the initial strength is developed quickly, and by adding a regular amount of the present emulsion, flexibility is imparted to the cured product. fruit! %1612
This is the case where CAs and the present emulsion were not added, and the strength development was slow and the flexibility of the cured product was low. Experiment 16 is
When this emulsion is not added, the flexibility of the cured product is low. Test No. 14 is a case where an excessive amount of emulsion is added, and the strength of the cured product is greatly reduced. Experiment/161
No. 6 is a case in which CAs are added in excess, and the flexibility of the cured product decreases.

実施例2 新潟県西頚城郡青海町の電気化学工業(株)青海工場内
において、実施例1の実験42の配分の補修材と市販の
アスファルトピッチ(日本道路製)を、直径20cm、
深さ10cmの道路破損部に充填し几(12月末、施工
時の気温は5°C)。施工終了3時間後に道路を開放し
たが、補修材便用部は4ケ月経過後も剥離等の異常は紹
められなかつ九が、アスファル)fソチ便用部は2週間
後に充填量の/2が散逸していた。
Example 2 At Denki Kagaku Kogyo Co., Ltd.'s Aomi factory in Aomi-cho, Nishikukugi-gun, Niigata Prefecture, the repair material distributed in Experiment 42 of Example 1 and commercially available asphalt pitch (manufactured by Nippon Road) were mixed into 20 cm diameter
Fill the damaged part of the road to a depth of 10cm (at the end of December, the temperature at the time of construction was 5°C). The road was opened 3 hours after the completion of construction, but no abnormalities such as peeling were reported in the repair material toilet area even after 4 months had passed, and asphalt) f Sochi toilet area was filled with 1/2 of the filling amount after 2 weeks. was dissipating.

〔発明の効果〕〔Effect of the invention〕

本発明の補修材は次の効果を奏するものである。 The repair material of the present invention has the following effects.

(1)  水硬性物質を便用しているため、下地が濡れ
ていても施工可能である。
(1) Since a hydraulic substance is used, construction can be performed even when the base is wet.

(2)低温下でも120分以内に硬化するため、冬季の
道路補修作業に適する。
(2) It cures within 120 minutes even at low temperatures, making it suitable for road repair work in winter.

(3)低Tg(−30°C以下)のポリマーを使用して
いるため、補修材に柔軟性(可とう性)があシ、下地の
動きに追随できる。
(3) Since a polymer with a low Tg (-30°C or lower) is used, the repair material has flexibility and can follow the movement of the underlying material.

Claims (1)

【特許請求の範囲】[Claims] (1)セメント100重量部、エチレン−アクリル酸エ
ステル−酢酸ビニルからなるガラス転移温度が−30℃
以下である水性共重合体エマルジョンを固形分換算で2
〜60重量部及びカルシウムアルミネート類2〜50重
量部を主成分とする道路補修材。
(1) 100 parts by weight of cement, composed of ethylene-acrylic ester-vinyl acetate, with a glass transition temperature of -30°C
The following aqueous copolymer emulsion is converted to solid content by 2
A road repair material whose main components are ~60 parts by weight and 2 to 50 parts by weight of calcium aluminates.
JP28779988A 1988-11-16 1988-11-16 Road-repairing material Pending JPH02137755A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP28779988A JPH02137755A (en) 1988-11-16 1988-11-16 Road-repairing material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28779988A JPH02137755A (en) 1988-11-16 1988-11-16 Road-repairing material

Publications (1)

Publication Number Publication Date
JPH02137755A true JPH02137755A (en) 1990-05-28

Family

ID=17721900

Family Applications (1)

Application Number Title Priority Date Filing Date
JP28779988A Pending JPH02137755A (en) 1988-11-16 1988-11-16 Road-repairing material

Country Status (1)

Country Link
JP (1) JPH02137755A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6926769B2 (en) * 2001-04-12 2005-08-09 Fosroc Mining International Limited Cementitous compositions and a method of their use
JP2013136477A (en) * 2011-12-28 2013-07-11 Taiheiyo Materials Corp Road repairing material

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6926769B2 (en) * 2001-04-12 2005-08-09 Fosroc Mining International Limited Cementitous compositions and a method of their use
JP2013136477A (en) * 2011-12-28 2013-07-11 Taiheiyo Materials Corp Road repairing material

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