JP2726474B2 - Lining material and method for manufacturing lining pipe using the same - Google Patents

Lining material and method for manufacturing lining pipe using the same

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Publication number
JP2726474B2
JP2726474B2 JP1035444A JP3544489A JP2726474B2 JP 2726474 B2 JP2726474 B2 JP 2726474B2 JP 1035444 A JP1035444 A JP 1035444A JP 3544489 A JP3544489 A JP 3544489A JP 2726474 B2 JP2726474 B2 JP 2726474B2
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JP
Japan
Prior art keywords
lining
weight
parts
water
pipe
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 - Fee Related
Application number
JP1035444A
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Japanese (ja)
Other versions
JPH02217342A (en
Inventor
幸男 笹川
正孝 佐藤
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
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Priority to JP1035444A priority Critical patent/JP2726474B2/en
Publication of JPH02217342A publication Critical patent/JPH02217342A/en
Application granted granted Critical
Publication of JP2726474B2 publication Critical patent/JP2726474B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Manufacturing Of Tubular Articles Or Embedded Moulded Articles (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はライニング材及びライニング管の製造方法に
関し、詳しくは上下水道用に供給される、鋼管や鋳鉄関
などの管内面にライニングするライニング材及びライニ
ング管の製造方法に関する。
Description: BACKGROUND OF THE INVENTION The present invention relates to a lining material and a method for manufacturing a lining pipe, and more particularly, to a lining material supplied to water and sewage systems and lining a pipe inner surface such as a steel pipe or a cast iron stake. And a method for manufacturing a lining tube.

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

従来から上下水道などに使用される鋼管や鋳鉄管の内
面には、防錆、耐久性向上及び上水道水等の水質安定化
のため、ライニングが施されている。
2. Description of the Related Art Conventionally, a lining is provided on an inner surface of a steel pipe or a cast iron pipe used for water supply and sewerage in order to prevent rust, improve durability, and stabilize water quality of tap water and the like.

このライニング材として、ポルトランドセメントモル
タルが用いられているが、上水道管に使用すると初期通
水時にモルタル中のアルカリ分が溶出し、水のpHが10以
上と著しく増加する課題があつた。
Portland cement mortar is used as the lining material. However, when used for water supply pipes, the alkali in the mortar elutes during the initial passage of water, and there is a problem that the pH of the water significantly increases to 10 or more.

このpH上昇を押え、酸性下でのモルタル層の破壊を防
止するため、ポルトランドセメントモルタルライニング
においては、通常、ライニング層表面にシールコート材
を塗布していた。
In order to suppress the rise in pH and prevent the mortar layer from being destroyed under acidic conditions, a seal coat material is usually applied to the surface of the lining layer in Portland cement mortar lining.

しかしながら、埋設による実使用においては、遊離炭
酸等を多く含む地下水や下水の様な酸性の水によりシー
ルコート材が剥離し、ライニング層表面が露出してpHが
上昇したり、剥れたシールコート材が管内や送水ポンプ
等に詰まつたり、上水道水中に遊離したり、上水道水に
悪臭がしたりする課題があつた。また、シールコート材
の剥離面からCa2+が溶出し、ライニング層が破壊し、耐
久性が低下するという課題もあつた。シールコート材を
施すことなく通水初期における水のpH上昇を押える方法
としてR2Oの少ないセメントと砂を用いた管内面のライ
ニング方法が提案されている(特開昭63−296874号公
報)。しかしながらこのライニング方法を用いると、pH
上昇は抑制できるが、アルミナセメントモルタル中のAl
が溶出して、初期通水時に可溶性Al量が著しく増加し、
飲料水が白濁する課題があつた。また、遠心成形をする
ため、内面にセメント分が多く偏析し酸性水に対して耐
久性が十分でないなどの課題があつた。
However, in actual use by embedding, the seal coat material is peeled off by acidic water such as groundwater or sewage containing a lot of free carbonic acid, and the surface of the lining layer is exposed and the pH rises. There was a problem that the material was clogged in the pipes, water pumps, etc., released into the tap water, and the tap water had a bad smell. Another problem is that Ca 2+ elutes from the peeled surface of the seal coat material, the lining layer is broken, and the durability is reduced. As a method for suppressing an increase in the pH of water in the early stage of passing water without applying a seal coat material, a lining method for the inner surface of a pipe using cement and sand with a small amount of R 2 O has been proposed (JP-A-63-296874). . However, using this lining method,
Although the rise can be suppressed, Al in alumina cement mortar
Is eluted, and the amount of soluble Al increases remarkably during initial water passage,
There was a problem that drinking water became cloudy. In addition, the centrifugal molding has a problem in that a large amount of cement segregates on the inner surface and the durability against acidic water is not sufficient.

特に飲料水水中の可溶性Alは、多量に摂取すると健康
上好ましくないという報告(金属、1985,55(7)、P63
〜65、佐藤敏彦及び朝日新聞1989・1月17日号等)があ
り少ない方が好ましい。
In particular, soluble Al in drinking water is reported to be unhealthy when taken in large quantities (Metal, 1985, 55 (7), P63
~ 65, Toshihiko Sato and Asahi Shimbun 1989, January 17, etc.)

従来のライニング管は、ポルトランドセメントを用い
ており、可溶性Alの原因となる水硬性カルシウムアルミ
ネートの3CaO・Al2O3が微量しか含まれないため可溶性A
l量は、シールコートしなくても0.2ppm以下の非常に低
いレベルであつた。しかしながら特開昭63−296874号公
報の様にアルミナセメントを用いると、CaO・Al2O3、Ca
O・2Al2O3及び12CaO・7Al2O3等の水硬性カルシウムアル
ミネートを主鉱物として含むため、可溶性Al量が著しく
増加する課題があつた。
Conventional lining pipe, is used Portland cement, soluble for hydraulic calcium aluminate 3CaO · Al 2 O 3 of which causes the soluble Al is not contained only trace amounts A
The l level was at a very low level of 0.2 ppm or less without a seal coat. However, when alumina cement is used as disclosed in JP-A-63-296874, CaO.Al 2 O 3 , Ca
To include O · 2Al 2 O 3 and hydraulic calcium aluminate such as 12CaO · 7Al 2 O 3 as the main mineral, there has been a problem that the amount of soluble Al is increased remarkably.

また、アルミナセメントは、ポルトランドセメントに
比べ水和初期の発熱量が多いため、モルタル硬化時にラ
イニング層表面の水分が蒸発し、水和水不足による未硬
化部分が発生し表面が粉化するという課題があつた。こ
のため、ライニング層表面を均一にするのに、厚く研磨
する必要があり、研磨や研磨粉の処分に多大な時間と労
力がかかるという課題があつた。
In addition, alumina cement generates more heat at the beginning of hydration than Portland cement.Therefore, the moisture on the lining layer surface evaporates when the mortar hardens, and the unhardened part due to lack of hydration water is generated and the surface is powdered. Atsuta. For this reason, in order to make the surface of the lining layer uniform, it is necessary to polish it thickly, and there is a problem that it takes a lot of time and labor to polish and dispose of the polishing powder.

本発明者らは上記各課題を解消すべく鋭意検討した結
果、通水初期における水のpH上昇、可溶性Al量の増加及
びモルタル硬化体の表面未硬化を防ぐためには、特定組
成のライニング材を使用することが有効であるとの知見
を得て本発明を完成するにいたつた。
The present inventors have conducted intensive studies to solve the above problems, and as a result, in order to prevent an increase in the pH of water in the initial stage of water flow, an increase in the amount of soluble Al, and uncured surface of the cured mortar, a lining material having a specific composition is used. The present inventors have found that it is effective to use them, and have completed the present invention.

〔課題を解決するための手段〕[Means for solving the problem]

即ち、本発明は、アルミナセメント85〜99重量部とシ
リカヒューム15〜1重量部とからなるバインダー、砂、
及び水を主成分とするライニング材であり、更に、無機
質膨張材と減水剤を併用するものであり、それらを使用
するライニング管の製造方法である。
That is, the present invention provides a binder comprising 85 to 99 parts by weight of alumina cement and 15 to 1 part by weight of silica fume, sand,
And a lining material containing water as a main component, and a combination of an inorganic expanding material and a water reducing agent, and a method for manufacturing a lining tube using the same.

以下、本発明を詳細に説明する。 Hereinafter, the present invention will be described in detail.

本発明にかかるアルミナセメント(以下ACという)
は、ボーキサイト、バイヤーアルミナ及びアルミナ残灰
等のアルミナ源と、生石灰、石灰石及び消石灰等のカル
シア源から、溶融法及び/又は焼成法によつて合成した
クリンカーを、ボールミル、ローラーミル及びオングミ
ル等の粉砕機で粉砕したものである。
Alumina cement according to the present invention (hereinafter referred to as AC)
Is a clinker synthesized from a source of alumina such as bauxite, Bayer alumina and alumina residual ash, and a source of calcia such as quicklime, limestone and slaked lime by a melting method and / or a firing method, such as a ball mill, a roller mill and an angmill. It is crushed by a crusher.

その鉱物組成は、CaOをC,Al2O3をAとすると、CA,C
A2,C3A、C12A7、C5A3及びC3A5等と示される水硬性カル
シウムアルミネートを主体とするものであつて、水和硬
化時にアルミナゲル(Al(OH))の生成の少ない、C/
A(モル比)≦1のものを主体とするACが好ましく、可
使時間、硬化性及び強度発現性の良好なCaO30〜40重量
%、Al2O340〜60重量%の水硬性カルシウムアルミネー
トが特に好ましい。
The mineral composition is CA, C, where CaO is C and Al 2 O 3 is A.
A 2, C 3 A, C 12 A 7, C 5 A 3 and C 3 shall apply essentially provided by a hydraulic calcium aluminate represented as A 5, etc., alumina gel upon hydration hardening (Al (OH) 3 ) Less generation of C /
A (molar ratio) ≦ 1 AC is preferable, and a hydraulic calcium aluminum of 30 to 40% by weight of CaO and 40 to 60% by weight of Al 2 O 3 having good pot life, curability and strength development. Nates are particularly preferred.

本発明にかかるシリカヒューム(以下SFという)と
は、一般に、シリコン、フェロシリコン、及び溶融シリ
カ等を製造する際に、副産物として生成する気化性シリ
カで、マイクロシリカ、シリカフラワー、及びシリカダ
スト等ともいわれるものである。
The silica fume (hereinafter referred to as SF) according to the present invention is generally a volatilizable silica produced as a by-product when producing silicon, ferrosilicon, fused silica, etc., such as micro silica, silica flour, and silica dust. It is also called.

特に本発明の目的を達成するには、SFのpHが重要であ
つて、pH≦8が好ましく、特にpHが6〜8の中性付近の
ものがより好ましい。
In particular, in order to achieve the object of the present invention, the pH of SF is important, and pH ≦ 8 is preferred, and those having a pH of 6 to 8 near neutrality are more preferred.

本発明でいうpHとは、室温にてSF2.0gをイオン交換水
200ml中に入れ、スターラーにて撹拌し得られたスラリ
ーのpHが平衡に達した時の値である。
The pH referred to in the present invention means that 2.0 g of SF is added to ion-exchanged water at room temperature.
It is a value when the pH of the slurry obtained in 200 ml and stirred with a stirrer reaches equilibrium.

SFのpHが8を越えるとライニング材として使用した
際、初期通水時のpHが上昇し、可溶性Al量も増加するた
め好ましくない。また、pHが6未満では、ACとの反応に
欠け、強度発現が悪くなり、耐久性が得られにくいた
め、好ましくない。更に、SFはACとの反応性の良好なBE
T比表面積10〜25m2/gのものが好ましく、SiO2含量80重
量%以上のものが長期強度が良好なため好ましい。
If the pH of SF exceeds 8, when used as a lining material, the pH during initial water passage increases and the amount of soluble Al increases, which is not preferable. On the other hand, when the pH is less than 6, the reaction with AC is lacking, the strength is deteriorated, and the durability is hardly obtained. Furthermore, SF is a BE with good reactivity with AC.
Those having a T specific surface area of 10 to 25 m 2 / g are preferable, and those having a SiO 2 content of 80% by weight or more are preferable because of good long-term strength.

本発明にかかるACとSFの配合割合は、AC85〜99重量
%、SF15〜1重量部の割合である。SF1重量部未満で
は、可溶性Al量の減少効果に欠け、15重量部を越えると
強度の発現性が悪く、遠心成形時にライニング層の締ま
りが悪くなる傾向がある。
The mixing ratio of AC and SF according to the present invention is 85 to 99% by weight of AC and 15 to 1 part by weight of SF. If the amount is less than 1 part by weight of SF, the effect of reducing the amount of soluble Al is lacking, and if it exceeds 15 parts by weight, the strength development is poor, and the tightness of the lining layer during centrifugal molding tends to be poor.

本発明にかかる無機膨張材(以下膨張材という)はカ
ルシウムサルホアルミネートや石膏等から成るエトリガ
イト生成系のものや、フツ化カルシウムや酸化カルシウ
ム等から成る石灰系のものが使用できる。
As the inorganic expanding material (hereinafter referred to as expanding material) according to the present invention, an etarigite-producing material composed of calcium sulfoaluminate or gypsum, or a lime-based material composed of calcium fluoride or calcium oxide can be used.

特にエトリンガイト生成系のものが可使時間が取れる
ため好ましい。
In particular, an ettringite-producing system is preferable because a pot life can be obtained.

ACとSFを配合して成るバインダーと膨張材の配合割合
は、バインダー85〜98重量部、膨張材15〜2重量部の割
合いであることが好ましく、特に、バインダー90〜96重
量部、膨張材10〜4重量部がより好ましい。
It is preferable that the blending ratio of the binder and the expander formed by blending AC and SF is 85 to 98 parts by weight of the binder and 15 to 2 parts by weight of the expander, and particularly, 90 to 96 parts by weight of the binder and the expander. 10 to 4 parts by weight are more preferred.

膨張材が15重量部を越えると、長時間使用した際、ラ
イニング層が膨張破壊を生じる傾向があり好ましくな
く、2重量部未満では膨張材としての効果に欠け、ライ
ニング層に収縮クラツクが発生する傾向があり好ましく
ない。
If the amount of the intumescent material exceeds 15 parts by weight, the lining layer will tend to expand and break when used for a long time, and if it is less than 2 parts by weight, the effect of the intumescent material will be lacking and shrinkage cracks will occur in the lining layer. There is a tendency and it is not preferable.

膨張材と粒度は、ACと同程度であることが好ましく、
ブレーン法で2,500cm2/g以上が好ましく、4,000〜6,000
cm2/gのものがより好ましい。ACより極端に粗いか又は
細かいと、遠心成形により偏析し、クラツクの原因にな
るため好ましくない。
The expansive material and particle size are preferably about the same as AC,
2,500 cm 2 / g or more is preferable in the Brain method, and 4,000 to 6,000
cm 2 / g is more preferred. If it is extremely coarse or finer than AC, it is not preferable because it segregates by centrifugal molding and causes cracks.

本発明にかかる減水剤は、リグニンスルホン酸塩系、
ナフタレンスルホン酸塩系、ナフタレンスルホン酸塩ホ
ルマリン縮合物系、メラミンスルホン酸塩ホルマリン縮
合物系、ポリカルボン酸塩系、リン酸系、ホウ酸系及び
オキシカルボン酸塩系等のものであつて、Alと難溶性の
塩を生成し、減水効果と可溶性Al抑制効果をあわせ持つ
ているリン酸系やホウ酸系が特に好ましく、具体的に
は、ヘキサメタリン酸、ピロリン酸、トリポリリン酸及
びホウ酸又はそれらのNa塩やK塩等である。
The water reducing agent according to the present invention is a lignin sulfonate type,
Naphthalene sulfonate type, naphthalene sulfonate formalin condensate type, melamine sulfonate formalin condensate type, polycarboxylate type, phosphoric acid type, boric acid type and oxycarboxylate type, etc. Phosphoric acid type or boric acid type, which forms a sparingly soluble salt with Al and has both a water reducing effect and a soluble Al suppressing effect, is particularly preferred, specifically, hexametaphosphoric acid, pyrophosphoric acid, tripolyphosphoric acid and boric acid or Na salt and K salt thereof.

各減水剤は単独もしくは併用でき、その使用量はバイ
ンダーと膨張剤の合計量(以下粉体という)100重量部
に対し、0.1〜5重量部の割合いであることが好まし
く、強度発現が良好な面から0.1〜2重量部が特に好ま
しい。
Each water reducing agent can be used alone or in combination. The amount of the water reducing agent is preferably 0.1 to 5 parts by weight based on 100 parts by weight of the total amount of the binder and the swelling agent (hereinafter referred to as powder). 0.1 to 2 parts by weight from the surface is particularly preferred.

本発明にかかる砂は、塩害や白華が発生しにくい川砂
や山砂が好ましく、海砂はNaClが多いため好ましくな
い。
The sand according to the present invention is preferably river sand or mountain sand in which salt damage or efflorescence is less likely to occur, and sea sand is not preferable because it contains a large amount of NaCl.

砂の使用量はバインダー又は粉体100重量部に対し、
砂100〜300重量部が通常使用され、管径により使い分け
される。例えば、100〜700φmmの管ではバインダー又は
粉体100重量部に対し砂100〜270重量部の割合いであ
る。
The amount of sand used is 100 parts by weight of binder or powder,
100-300 parts by weight of sand is usually used, and is used depending on the pipe diameter. For example, a ratio physician sand 100 to 270 parts by weight per 100 parts by weight of the binder or powder in tube 100 to 700 phi mm.

本発明では、上記材料をパン型ミキサーやパドルミキ
サー等のミキサーにて水と混練りし、モルタルの練り上
がり温度を25℃以下にするのが好ましく、20℃付近が特
に好ましい。
In the present invention, the above materials are kneaded with water in a mixer such as a pan mixer or a paddle mixer, and the kneading temperature of the mortar is preferably 25 ° C. or lower, and particularly preferably around 20 ° C.

25℃を越えると偽凝結を生じやすく、可使時間が取れ
にくくなり好ましくない。また練り上がり温度が高い
と、AC水和物の転移反応に伴うAl(OH)の生成量が多
くなり、可溶性Al量が増加するため好ましくない。練り
上がり温度が、例えば、5℃以下の様に低いと、硬化遅
れが発生し、強度発現が悪いため低くすぎても好ましく
ない。
If the temperature exceeds 25 ° C., false coagulation tends to occur, and it is difficult to obtain a pot life, which is not preferable. On the other hand, a high kneading temperature is not preferable because the amount of Al (OH) 3 produced by the transfer reaction of the AC hydrate increases and the amount of soluble Al increases. If the kneading temperature is as low as, for example, 5 ° C. or less, curing delay occurs and the strength is poor, so that it is not preferable to be too low.

モルタルのフロー値は、フローテーブルを用いた15回
タツプフロー値で200mm以上が好ましく、特に240〜280m
mが好ましい。フロー値が200mm未満では遠心成形時に、
管内面に均一なライニング層が成形されにくく、280mm
を越えると、遠心成形によるライニング層の締りが悪
く、ペースト層が分離しクラツクや剥離が発生し易い傾
向があり好ましくない。
The mortar flow value is preferably 200 mm or more as a 15-step tap flow value using a flow table, particularly 240 to 280 m
m is preferred. If the flow value is less than 200 mm, during centrifugal molding,
It is difficult to form a uniform lining layer on the inner surface of the pipe, 280 mm
If the ratio exceeds the above range, the lining layer will not be tightly tightened by centrifugal molding, and the paste layer will be separated, and cracks and peeling will tend to occur, which is not preferred.

遠心成形は通常20G以上で行われるが、本発明では、
特に、50〜70Gがライニング層の締りが良く好ましい。5
0G未満では、遠心成形後のライニング層の締りが悪く、
レイタンスの浮きも不十分であり、70Gを越えるとペー
スト層が分離しクラツクが発生し易くなる傾向があり好
ましくない。
Centrifugal molding is usually performed at 20G or more, but in the present invention,
In particular, 50 to 70 G is preferable because the lining layer is tight. Five
If it is less than 0G, the lining layer after centrifugal molding is poorly tightened,
The lifting of the latency is insufficient, and if it exceeds 70 G, the paste layer tends to separate and cracks are likely to occur, which is not preferable.

最高Gによる遠心成形時間は3分以上が好ましく、ラ
イニング層が均一になり、締りも良好であるため好まし
い。特に、遠心成形時間5分以上がライニング層からの
水抜けが安定し好ましい。
The centrifugal molding time at the maximum G is preferably 3 minutes or more, which is preferable because the lining layer becomes uniform and the tightening is good. In particular, a centrifugal molding time of 5 minutes or more is preferable because the water drainage from the lining layer is stable.

遠心成形によるライニングした管は、相対湿度60%R.
H.以上の加湿条件下で一次養生するのが好ましく、更に
好ましくは80%R.H.以上である。また、養生温度は25℃
以下が好ましく、20℃近辺で低温加湿養生するのがより
好ましい。
Tubes lined by centrifugal molding have a relative humidity of 60% R.
It is preferable to perform primary curing under humidification conditions of H. or higher, and more preferably 80% RH or higher. Curing temperature is 25 ℃
The following is preferable, and it is more preferable to perform low-temperature humidification curing at around 20 ° C.

養生時間はライニング完了直後から4時間以上が好ま
しく、セメントの水和発熱が完了するまで行うのが更に
好ましい。
The curing time is preferably at least 4 hours immediately after the completion of the lining, and more preferably until the heat of hydration of the cement is completed.

上記条件以外での加湿養生ではライニング層表面に未
硬化部分が発生し粉化したり、可溶性Al量が低下しない
ため好ましくない。
Humidification and curing under conditions other than the above conditions are not preferable because uncured portions are generated on the surface of the lining layer and powdered, and the amount of soluble Al does not decrease.

一次養生が完了したライニング管は、常法により表面
を均一に研磨後、常温気乾にて2日以上二次養生し、埋
設使用される。研磨厚は管径にもよるが、通常、表面か
ら0.5〜3mm程度である。
After the primary curing is completed, the surface of the lining tube is uniformly polished by an ordinary method, then secondary cured by air drying at room temperature for 2 days or more, and used for burying. The polishing thickness depends on the pipe diameter, but is usually about 0.5 to 3 mm from the surface.

二次養生期間は、初期通水のpH及び可溶性Al量が十分
低下する4日間以上行うのが好ましく、6日以上が特に
好ましい。
The secondary curing period is preferably performed for 4 days or more when the initial water flow and the amount of soluble Al are sufficiently reduced, and particularly preferably 6 days or more.

本発明の方法により実施される管は、通常、鋳鉄管が
使用されるが、予め従来法によりライニング層を成層し
た管を用い、二層以上のライニング層を有するものを使
用することは可能である。
As the pipe to be carried out by the method of the present invention, a cast iron pipe is usually used, but it is possible to use a pipe having a lining layer formed in advance by a conventional method, and to use a pipe having two or more lining layers. is there.

また、ライニング管の耐酸性や長期安定性等の耐久性
を向上させるために、高炉水枠スラグ粉末、石灰石粉末
及びフライアッシュ等を添加、混合使用しても良い。
Further, blast furnace water frame slag powder, limestone powder, fly ash and the like may be added and mixed to improve durability of the lining pipe such as acid resistance and long-term stability.

これらを使用する場合はバインダ又は粉体との合計量
100重量部に対し70重量部以下が好ましい。70重量部を
越えるとライニング層の強度が低下し、耐久性が低下す
るため好ましくない。
When using these, the total amount with binder or powder
70 parts by weight or less is preferable for 100 parts by weight. If the amount exceeds 70 parts by weight, the strength of the lining layer decreases, and the durability decreases, which is not preferable.

更に、低pHを得るためには硫酸アルミニウムの添加も
有効である。
Further, to obtain a low pH, addition of aluminum sulfate is also effective.

〔実施例〕〔Example〕

以下本発明を実施例にて詳しく説明する。 Hereinafter, the present invention will be described in detail with reference to Examples.

実施例1 ACとSFを表−1のように配合し、小型オムニミキサー
(千代田技研工業製)により55分混合してバインダーを
製造した。
Example 1 AC and SF were blended as shown in Table 1, and mixed with a small omni mixer (manufactured by Chiyoda Giken Kogyo) for 55 minutes to produce a binder.

このバインダー100重量部と川砂200重量部をパン型ミ
キサーにて3分間空練り後、260±20mmのフロー値にな
る様に水道水を加え、5分間混練りし、練り上がり温度
20±2℃のモルタルを作製した。
After 100 parts by weight of this binder and 200 parts by weight of river sand are kneaded with a pan-type mixer for 3 minutes, tap water is added to a flow value of 260 ± 20 mm, and the mixture is kneaded for 5 minutes.
A mortar at 20 ± 2 ° C. was prepared.

このモルタルを遠心成形機により、100φmm×500lmm
の鋳鉄管内面に50G−5分間の条件で厚さ5mmのライニン
グ層を形成した。
The mortar by centrifugal molding machine, 100 φ mm × 500 l mm
A lining layer having a thickness of 5 mm was formed on the inner surface of the cast iron tube under the conditions of 50 G for 5 minutes.

ライニング完了後、20℃100%R.H.の加湿器内に入
れ、12時間一次養生行つた後、旋盤にて表面を1mm研磨
し、更に6日間常温気乾条件下で二次養生し、本発明の
ライニング管を得た。その物性を表−1に併記する。
After completion of lining, put in a humidifier at 20 ° C and 100% RH, perform primary curing for 12 hours, then grind the surface with a lathe for 1 mm, and further secondary cure under normal temperature air-dry condition for 6 days. A lining tube was obtained. The physical properties are also shown in Table 1.

比較のため、従来技術として、商品名「デンカアルミ
ナセメント2号」電気化学工業社製100重量部と川砂200
重量部をパン型ミキサーにて3分間空練り後、260±20m
mのフロー値になる様に水道水を加え、5分間混練り
し、練り上がり温度20±2℃のモルタルを作製した。
For comparison, 100 parts by weight of Denka Alumina Cement No. 2 manufactured by Denki Kagaku Kogyo Co., Ltd. and 200
After kneading the parts by weight with a bread mixer for 3 minutes, 260 ± 20m
Tap water was added so as to obtain a flow value of m, and kneaded for 5 minutes to prepare a mortar having a kneading temperature of 20 ± 2 ° C.

このモルタルを遠心成形機により100φmm×500lmmの
鋳鉄管内面に40G−2分間の条件で厚さ5mmのライニング
層を形成した。ライニング完了後常温気乾条件にて24時
間一次養生行つた後ライニング層表面に水道水を散水し
つつサンドペーパーにて研磨処理を施し0.6mm表面を研
磨した。
To form a lining layer having a thickness of 5mm at the conditions of 40G-2 min cast iron pipe surface of 100 φ mm × 500 l mm by the mortar centrifugal molding machine. After completion of the lining, primary curing was performed for 24 hours under the condition of air drying at room temperature, and then the surface of the lining layer was polished with sandpaper while sprinkling tap water on the surface of the lining layer to polish the 0.6 mm surface.

その後、更に、常温気乾条件にて6日間二次養生し、
ライニング管を作製した。
After that, it is further cured for 6 days under normal temperature and air drying condition,
A lining tube was made.

<測定方法> (1)フロー値;フローテーブルにより15回タツプした
後のモルタルの広がり径 (2)強度;4×4×16cmテストピースによる圧縮強度 (3)pH;二次養生後のライニング管内面をイオン交換
水により洗浄後イオン交換水3,000mlを入れ、24時間、2
0℃にて浸漬しこの浸漬水のpHとした。
<Measurement method> (1) Flow value; Spread diameter of mortar after tapping 15 times with a flow table (2) Strength; Compressive strength with 4 × 4 × 16 cm test piece (3) pH; Inside lining pipe after secondary curing After washing the surface with ion-exchanged water, add 3,000 ml of ion-exchanged water,
It was immersed at 0 ° C. and adjusted to the pH of the immersion water.

(4)可溶性Al量;pH測定後の浸漬水をICPにて分析した
値。
(4) Soluble Al content; value obtained by analyzing immersion water after pH measurement by ICP.

<使用材料> AC−a:商品名「デンカアルミナセメント1号」、電気化
学工業社製CaO36.5重量%,Al2O353.5重量% b: 〃 「デンカアルミナセメント2号」電気化学
工業社製CaO33.0重量%,Al2O348.5重量% AC−c:商品名「デンカハイアルミナセメント」CaO25.5
重量%、Al2O373.5重量% SF−d:シリカヒユーム、pH8.3,BET22m2/g,SiO283.1%、
エルケム社製 e:シリカヒユーム、pH7.8,BET24m2/g,SiO293.1%、
エルケム社製 f:シリカヒユーム、pH6.8,BET21m2/g,SiO297.2%、
エルケム社製 砂 :熊本県玉名産川砂 フライアッシュ:pH10.4、BET0.7m2/g、SiO261.4%、関
電化工社製 シリカ:pH6.1、BET0.1m2/g、SiO299.0%、珪石粉 実施例2 バインダーと膨張材を表−2のように配合し、小型オ
ムニミキサーにより55分混合して組成物を製造した。
<Materials used> AC-a: Trade name “DENKA Alumina Cement No. 1”, CaO 36.5 wt%, Al 2 O 3 53.5 wt% manufactured by Denki Kagaku b: b “DENKA Alumina Cement No. 2” Denki Kagaku Kogyo 33.0% by weight of CaO, 48.5% by weight of Al 2 O 3 AC-c: Trade name “DENKA HIGH Alumina Cement” CaO 25.5
Weight%, Al 2 O 3 73.5 weight% SF-d: silica fume, pH 8.3, BET22m 2 / g, SiO 2 83.1%,
Erukemu manufactured by e: Shirikahiyumu, pH7.8, BET24m 2 / g, SiO 2 93.1%,
Erukemu Co., Ltd. f: Shirikahiyumu, pH6.8, BET21m 2 / g, SiO 2 97.2%,
Elchem sand: Tamana river sand, Kumamoto Prefecture Fly ash: pH 10.4, BET 0.7 m 2 / g, SiO 2 61.4%, Kanden Kako silica: pH 6.1, BET 0.1 m 2 / g, SiO 2 99.0% , Silica powder Example 2 A composition was manufactured by blending a binder and an expanding material as shown in Table 2 and mixing them for 55 minutes using a small omni mixer.

この組成物100重量部と川砂200重量部をパン型ミキサ
ーにて3分間空練り後所定量の減水剤を添加し、フロー
値260±20mmになる様に水道水を加え、5分間混合し、
練り上がり温度20±2℃のモルタルを作製した。
100 parts by weight of this composition and 200 parts by weight of river sand are kneaded with a pan mixer for 3 minutes, then a predetermined amount of a water reducing agent is added, tap water is added so that the flow value becomes 260 ± 20 mm, and mixed for 5 minutes.
A mortar having a kneading temperature of 20 ± 2 ° C. was prepared.

このモルタルを用い実施例1と同様にライニング管を
得た。その物性を表−2に併記する。
Using this mortar, a lining tube was obtained in the same manner as in Example 1. The physical properties are also shown in Table-2.

尚、物性の測定と材料は実施例1に準じその他は下記
に準じた。
The measurement of physical properties and materials were the same as in Example 1, and the others were as follows.

<測定方法> (1)ライニング層の締り;ライニング終了後触指にて
良悪を判定した。
<Measurement Method> (1) Tightening of the lining layer;

(2)表面クラツク;常温気乾条件下で50日二次養生し
たライニング管の表面のクラツクの有無を可視にて判定
した。
(2) Surface cracks: The presence or absence of cracks on the surface of the lining tube that was secondarily cured for 50 days under normal temperature air-dry conditions was visually determined.

<使用材料> 膨張剤g:商品名「デンカCSA20」、電気化学工業製 h:商品名「エクスパン製品用」、小野田セメント
製 j:II型無水石膏、セントラル硝子製 減水剤k:商品名「マイテイ150」花王石鹸製 l:商品名「ヴインソル80」山宗化学製 m:商品名「ポゾリスNo.5L」ポゾリス製 n:ヘキサメタリン酸Na、関東化学製試薬一級 p:ヘキサメタリン酸K、関東化学製試薬一級 q:トリポリリン酸Na、関東化学製試薬一級 減水剤r:ホウ酸、関東化学製試薬一級 s:ホウ砂、関東化学製試薬一級 実施例3 実験No.2−4の組成物100重量部と川砂200重量部をパ
ン型ミキサーで3分間空練り後、フロー値260±20mmに
なる様に水道水を加え、5分間混合し、練り上がり温度
20±2℃のモルタルを作製した。
<Materials> Swelling agent g: Trade name "DENKA CSA # 20", manufactured by Denki Kagaku Kogyo h: trade name "for Expan products", manufactured by Onoda Cement j: type II anhydrous gypsum, manufactured by Central Glass Water reducer k: trade name "Mighty 150" made by Kao Soap l: Trade name "Vinsol 80" made by Yamamune Chemical m: Trade name "Pozoris No.5L" Made by Pozoris n: Na hexametaphosphate, Kanto Chemical reagent first class p: Hexametaphosphate K, Kanto Chemical Reagent grade q: Na tripolyphosphate, Kanto Chemical grade 1 Water reducing agent r: Boric acid, Kanto Chemical grade 1 s: Borax, Kanto Chemical grade 1 Example 3 After 100 parts by weight of the composition of Experiment No. 2-4 and 200 parts by weight of river sand were kneaded with a pan-type mixer for 3 minutes, tap water was added to a flow value of 260 ± 20 mm, and mixed for 5 minutes. Kneading temperature
A mortar at 20 ± 2 ° C. was prepared.

このモルタルを遠心成形機により100φmm×500lmmの
鋳鉄管内面に表−3に示す条件で厚さ5mmのライニング
層を形成した。
The mortar was formed lining layer having a thickness of 5mm under the conditions shown in Table 3 in the cast iron pipe surface of 100 φ mm × 500 l mm by centrifugal molding machine.

ライニング完了後の処理は実施例1に準じ、物性の測
定と材料は、実施例1及び2に準じ、その他は下記によ
り行つた。その物性を表−3に併記する。
The processing after completion of the lining was performed in accordance with Example 1, the measurement of physical properties and materials were performed in accordance with Examples 1 and 2, and the others were performed as follows. The physical properties are also shown in Table-3.

<測定方法> (1)ライニング層から水抜け;目視にて良悪を判定し
た。
<Measurement Method> (1) Drainage of water from the lining layer;

(2)ライニング層の仕上がり; 〃 〃 実施例4 実施例3の方法で作製したモルタルを遠心成形機によ
り100φmm×500lmm鋳鉄管内面に50G−5分間の条件で厚
さ5mmのライニング層を形成した。
(2) Finish of lining layer; To form a lining layer having a thickness of 5mm under the conditions of Example 4 by mortar centrifugal molding machine manufactured by the method of Example 3 100 φ mm × 500 l mm cast iron pipe surface 50G-5 minutes.

ライニング完了後表−4の条件下で一次養生行つた後
旋盤にて表面を1mm研磨し、更に所定の条件下で二次養
生を行い、ライニング管を得た。
After completion of the lining, primary curing was performed under the conditions shown in Table-4, and then the surface was polished by a lathe with a thickness of 1 mm. Further, secondary curing was performed under predetermined conditions to obtain a lining tube.

各養生条件及びライニング管の物性を表−4に示す。
物性の測定及び材料は実施例2に準じた。
Table 4 shows the curing conditions and physical properties of the lining tube.
The measurement of physical properties and the material were in accordance with Example 2.

〔発明の効果〕 以上から明らかな様に、本発明により製造した管はシ
ールコートを施すことなく初期通水のpHを低く押えるこ
とができ、従来のAC使用ライニング管に比べ、可溶性Al
量を著しく減少できる。
[Effects of the Invention] As is clear from the above, the pipe manufactured according to the present invention can keep the initial water flow pH low without applying a seal coat, and has a higher soluble Al content than the conventional lining pipe using AC.
The amount can be significantly reduced.

また、一次養生時に発生していたライニング表面の粉
化を防止でき、表面仕上げの良好なライニング管が得ら
れる。
Further, powdering of the lining surface generated during the primary curing can be prevented, and a lining tube having a good surface finish can be obtained.

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】アルミナセメント85〜99重量部とシリカヒ
ューム15〜1重量部とからなるバインダーと、砂、及び
水を主成分とするライニング材。
1. A lining material containing 85 to 99 parts by weight of alumina cement and 15 to 1 parts by weight of silica fume, sand and water as main components.
【請求項2】請求項1記載のライニング材を遠心力成形
法によって管内面にライニングし、加温養生により該ラ
イニング層を硬化することを特徴とするライニング管の
製造方法。
2. A method for manufacturing a lining pipe, comprising: lining the lining material according to claim 1 on an inner surface of the pipe by a centrifugal force forming method, and curing the lining layer by heating and curing.
【請求項3】請求項1記載のバインダー85〜98重量部、
無機質膨張材15〜2重量部、及びバインダーと無機質膨
張材の合計100重量部に対して、減水剤0.1〜5重量部か
らなる組成物、砂、並びに、水を主成分とするライニン
グ材。
3. 85 to 98 parts by weight of the binder according to claim 1,
A lining material mainly composed of 15 to 2 parts by weight of an inorganic expander and 0.1 to 5 parts by weight of a water reducing agent with respect to 100 parts by weight of a total of a binder and an inorganic expander.
【請求項4】請求項3記載のライニング材を遠心力成形
法によって管内面にライニングし、加温養生により該ラ
イニング層を硬化することを特徴とするライニング管の
製造方法。
4. A method for manufacturing a lining pipe, comprising: lining the lining material according to claim 3 on the inner surface of the pipe by a centrifugal molding method; and curing the lining layer by heating and curing.
JP1035444A 1989-02-15 1989-02-15 Lining material and method for manufacturing lining pipe using the same Expired - Fee Related JP2726474B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1035444A JP2726474B2 (en) 1989-02-15 1989-02-15 Lining material and method for manufacturing lining pipe using the same

Publications (2)

Publication Number Publication Date
JPH02217342A JPH02217342A (en) 1990-08-30
JP2726474B2 true JP2726474B2 (en) 1998-03-11

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Country Link
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101265016B (en) * 2008-04-17 2012-07-04 淄博嘉环耐火材料有限公司 Rotating pipe and manufacturing method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2943169A1 (en) * 2009-03-10 2010-09-17 Sediver PROCESS FOR MANUFACTURING A SEALING MORTAR FOR HIGH-VOLTAGE ELECTRIC INSULATOR METAL PARTS IN GLASS OR PORCELAIN

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5825568B2 (en) * 1976-02-03 1983-05-28 電気化学工業株式会社 Lining method
JPH0738968B2 (en) * 1987-05-29 1995-05-01 株式会社クボタ Inner surface lining method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101265016B (en) * 2008-04-17 2012-07-04 淄博嘉环耐火材料有限公司 Rotating pipe and manufacturing method thereof

Also Published As

Publication number Publication date
JPH02217342A (en) 1990-08-30

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