JPS58217455A - Anhydrous gypsum composition for flow-spread floor material and construction therefor - Google Patents

Anhydrous gypsum composition for flow-spread floor material and construction therefor

Info

Publication number
JPS58217455A
JPS58217455A JP10099482A JP10099482A JPS58217455A JP S58217455 A JPS58217455 A JP S58217455A JP 10099482 A JP10099482 A JP 10099482A JP 10099482 A JP10099482 A JP 10099482A JP S58217455 A JPS58217455 A JP S58217455A
Authority
JP
Japan
Prior art keywords
weight
type
parts
anhydrite
blast furnace
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.)
Granted
Application number
JP10099482A
Other languages
Japanese (ja)
Other versions
JPS6346022B2 (en
Inventor
薗田 喜造
岩崎 喜男
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.)
Daikin Industries Ltd
Shimizu Construction Co Ltd
Original Assignee
Daikin Industries Ltd
Shimizu Construction Co Ltd
Daikin Kogyo Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daikin Industries Ltd, Shimizu Construction Co Ltd, Daikin Kogyo Co Ltd filed Critical Daikin Industries Ltd
Priority to JP10099482A priority Critical patent/JPS58217455A/en
Publication of JPS58217455A publication Critical patent/JPS58217455A/en
Publication of JPS6346022B2 publication Critical patent/JPS6346022B2/ja
Granted 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
    • C04B28/14Compositions 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 calcium sulfate cements
    • C04B28/16Compositions 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 calcium sulfate cements containing anhydrite, e.g. Keene's cement

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)
  • On-Site Construction Work That Accompanies The Preparation And Application Of Concrete (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本゛発明は、流し延べ床材用無水石膏組成物およびその
施工法に関し、更に詳しくはI’l型無水石膏、高炉上
メ、ン(および硬化促進剤を含んで成る組成物およびそ
の施工法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to anhydrous gypsum compositions for cast flooring and a method for applying the same, and more specifically, the present invention relates to anhydrous gypsum compositions for cast flooring and methods for applying the same. The present invention relates to a composition comprising the same and a method for applying the same.

II型無水石膏は、水を加えても直ちに工水石膏となら
ないため、硬化に極めて長時間を要するので、硫酸カリ
ウムなどのいわゆる硬化促進剤の助けを借りて比較的短
時間に硬化させられる。
Type II anhydrite does not immediately turn into water gypsum even when water is added to it, so it takes a very long time to harden, so it can be hardened in a relatively short time with the help of a so-called hardening accelerator such as potassium sulfate.

11型無水石膏は、これに水酸化カルシウムまたは酸化
カルシウムを水酸化カルシウム換算で該石膏の0.2〜
5重量%、促進剤を0.5〜7.5重量%、その他の添
加剤(たとえば流動化剤)を適宜加えた組成物として床
面形成材に用いられている。
Type 11 anhydrite contains calcium hydroxide or calcium oxide in an amount of 0.2 to 0.2 of the gypsum in terms of calcium hydroxide.
5% by weight, 0.5 to 7.5% by weight of an accelerator, and other additives (for example, a fluidizing agent) as appropriate for use in floor forming materials.

すなわち、この組成物に水を加えてスラリーとし、これ
を床面上に流し延べ、自然乾燥して床面を形成する。
That is, water is added to this composition to form a slurry, which is poured onto a floor surface and air-dried to form a floor surface.

II型無水石膏組成物は、このように床面形成に用いら
れるが、その際、形成された床面が早期に硬化し、その
床面の加工、たとえばPタイル張りを早期に施工するこ
とがで終ること力5要望されている。たとえば、ビル建
設におり−ては、床面の形成に続けて、たとえばPタイ
ル張りを施工し、工期を短縮することが望まれている。
The type II anhydrite composition is thus used to form a floor surface, but at that time, the formed floor surface hardens early, making it difficult to process the floor surface, such as P tiling, at an early stage. It is requested that the force end with 5. For example, in the construction of a building, it is desired to shorten the construction period by constructing, for example, P tiles after forming the floor surface.

本発明の目的は、前記要望に応えることにある。An object of the present invention is to meet the above demand.

前記目的は、 (a)II型無水石膏        150重量部(
b)高炉セメントA種またはB種 75〜175重量部
(c)硬化促進剤       0.75〜7.5重量
部から成る流し延べ床材用II型無水石膏組成物により
達成することができる。
(a) 150 parts by weight of type II anhydrite (
b) 75 to 175 parts by weight of blast furnace cement type A or B; (c) hardening accelerator 0.75 to 7.5 parts by weight. This can be achieved by a type II anhydrite composition for cast flooring.

本発明の組成物を用いることにより、施工後3日で施工
後28日の表面引張り強度の80%以上に相当する強度
の床面が形成され、したがって早期床面加工をすること
ができる床面を形成することができる。
By using the composition of the present invention, a floor surface with a strength equivalent to 80% or more of the surface tensile strength on 28 days after construction is formed in 3 days after construction, and therefore a floor surface that can be subjected to early floor processing. can be formed.

高炉セ)1>トは、JIS  R’5211(1955
)に規定されているものであって、急冷砕した高炉スラ
グとボルトランドセメントタリンヵとを混ぜ、適量の石
膏を加え、粉砕して粉末としたものである。ボルトラン
ドセメントタリンヵの割合は、重量で高炉上メートの3
0%以上であることを要する。高炉セメントとしてはA
種、B種および0種が市販されており、それぞれにおけ
る高炉スラグの配合割合は、次のとおりである。
Blast furnace
), which is made by mixing rapidly cooled and crushed blast furnace slag with Boltland cement tarinka, adding an appropriate amount of gypsum, and pulverizing it into powder. The proportion of Boltland cement tarinka is 3% of blast furnace top mate by weight.
It must be 0% or more. A as blast furnace cement
Types B, B and 0 are commercially available, and the blending ratio of blast furnace slag in each is as follows.

高炉スラグ 高炉セメン)A種      30重量%以下/、  
 Bm    30−60重量%〃  0種   60
〜70重量% 本発明においては、このうちのA種およびB種を用い、
II型無水石膏150重量部に対して75〜175重量
部を配合する。普通ポルトランドセメント、高炉セメン
トσ種または水砕スラグを配合したときは、十分には早
期に硬化せず、早期には十分な表面引張り強度が得られ
ない。また、配合量は、75重量部より少ないときは、
早期には十分な表面引張り強度が得られず、175重量
部より多いと鯵も、早期には十分な表面引張り強度が得
られない。
Blast furnace slag blast furnace cement) Type A 30% by weight or less/
Bm 30-60% by weight〃 Type 0 60
~70% by weight In the present invention, type A and type B of these are used,
75 to 175 parts by weight is added to 150 parts by weight of type II anhydrite. When ordinary Portland cement, blast furnace cement σ type, or granulated slag is mixed, it does not harden sufficiently early and sufficient surface tensile strength cannot be obtained at an early stage. In addition, when the blending amount is less than 75 parts by weight,
Sufficient surface tensile strength cannot be obtained at an early stage, and if the amount exceeds 175 parts by weight, sufficient surface tensile strength cannot be obtained at an early stage.

硬化促進剤としては、硫酸カリウム、カリミaウバン、
硫酸アルミニウムなどが例示でき、II型無水石膏15
0重1部に対して0.75〜?、5重量部を配合する。
As hardening accelerators, potassium sulfate, potassium chloride,
Examples include aluminum sulfate, type II anhydrite 15
0.75 to 1 part of 0 weight? , 5 parts by weight.

本発明は、以上述べたとおり、II型無水石膏に高炉セ
メントA種またはB種および硬化促進剤を配合した流し
延べ床材用組成物であり、水を加えて床面を形成するも
のであるが、本発明においても、従来の床面形成用の石
膏組成物に用い−られる各種添加剤の1種またはそれ以
上を適宜加えることがで終る。かかる添加剤には、骨材
、アルカリ剤、流動化剤、保水剤、消泡剤、膨張剤など
がある。
As described above, the present invention is a cast flooring composition comprising Type II anhydrite mixed with blast furnace cement type A or B and a hardening accelerator, which is used to form a floor surface by adding water. However, in the present invention, one or more of the various additives used in conventional gypsum compositions for forming floor surfaces are appropriately added. Such additives include aggregates, alkaline agents, fluidizing agents, water retention agents, antifoaming agents, swelling agents, and the like.

骨材には、砕砂、川砂なとがあり、砕砂では、砕砂5号
〜8号を”II型無水石膏150重量部に対して0〜1
75重量部加えること力動きる。そのうち、5号および
6号が好ましく、5号の場合は、175重量部まで、6
号の場合は、120重量部まで、8号の場合は、75重
量部までが好ましい。
Aggregates include crushed sand and river sand. For crushed sand, crushed sand No. 5 to No.
Add 75 parts by weight to move the force. Among them, No. 5 and No. 6 are preferred, and in the case of No. 5, up to 175 parts by weight, 6
In the case of No. 8, it is preferably up to 120 parts by weight, and in the case of No. 8, up to 75 parts by weight.

アルカリ剤には、i石灰または生石灰があり、■型無水
石膏150重量部に対して0〜30重量部の添加量がよ
い。
The alkaline agent includes i-lime or quicklime, and is preferably added in an amount of 0 to 30 parts by weight per 150 parts by weight of type 1 anhydrite.

流動化剤には、メラミンスルホン酸ホルムアルデヒド縮
合物ナトリウム塩、2,2°−ツメチル−5゜5゛−ジ
メチルスルホジフェニルエーテルホルムアルデヒド縮合
物ナトリウム塩、クレゾールスルホン酸ホルムアルデヒ
ド縮合物ナトリウム塩、β−ナフタリンスルホン酸ホル
ムアルデヒド縮合物ナトリウム塩などがあり、メルメン
トF−11)、メルメントF−20(以上昭和電工株式
会社製)、マイティFD(花王百齢株式会社製)などが
市販されている。流動化剤の添加量はII型無水石膏1
50重量部に対して1〜4重量部が好ましい。
The fluidizing agent includes sodium salt of melamine sulfonic acid formaldehyde condensate, sodium salt of 2,2°-tmethyl-5゜5゛-dimethylsulfodiphenyl ether formaldehyde condensate, sodium salt of cresol sulfonic acid formaldehyde condensate, and β-naphthalene sulfonic acid. There are formaldehyde condensate sodium salts, and Melment F-11), Melment F-20 (manufactured by Showa Denko Co., Ltd.), Mighty FD (manufactured by Kao Hyakurei Co., Ltd.), and the like are commercially available. The amount of fluidizing agent added is type II anhydrite 1
It is preferably 1 to 4 parts by weight per 50 parts by weight.

保水剤には、メチルセルロース類があす、x1型無水石
膏150重量部に対して0.3〜1.0重量部添加する
のが好ましい。
It is preferable that 0.3 to 1.0 parts by weight of methylcellulose be added to the water retention agent based on 150 parts by weight of x1 type anhydrite.

消泡剤には、シリコン系の界面活性剤があり、II型無
水石膏150重量部に対して0.1〜0.5重量部添加
するのが好ましい。
Antifoaming agents include silicone surfactants, and it is preferable to add 0.1 to 0.5 parts by weight per 150 parts by weight of type II anhydrite.

膨張剤には、各種の膨張セメントがあり、II型無水石
膏150重量部に対して0〜7.5重量部添加するのが
よい。
Expanding agents include various types of expanding cements, and it is preferable to add 0 to 7.5 parts by weight per 150 parts by weight of type II anhydrite.

本発明組成物から床面を形成するには、本発明組成物お
よび他の添加剤に水を加えて、または、水に本発明組成
物および他の添加剤を加えてスラリーを形成し、これを
床面に流し込めばよし1゜流し込んだ後は、十分な硬度
が得られるまで養生すればよい。
To form a floor surface from the composition of the present invention, the composition of the present invention and other additives are added to water, or the composition of the present invention and other additives are added to water to form a slurry. All you have to do is pour it onto the floor. After pouring it for 1 degree, you can cure it until it has sufficient hardness.

ここにおいて、本発明組成物および他の添加剤と水との
割合は、70−値(後述の方法で測定)が200±20
IlII+1、好ましくは200±15mm、特に20
0土10sunとなるようにするのがよい。
Here, the ratio of the composition of the present invention and other additives to water has a 70-value (measured by the method described below) of 200±20.
IlII+1, preferably 200±15 mm, especially 20
It is best to set it to 0 soil and 10 sun.

次に実施例および比較例を示し、本発明を具体的に説明
する。一 実施例および比較例における各特性の測定方法は、次の
とおりである。
Next, examples and comparative examples will be shown to specifically explain the present invention. The method for measuring each characteristic in one example and comparative example is as follows.

ブリ−ジング 1000mlのメスシリンダーに調合直後のスラリー1
0100Oを充填し、その後30分間に生ずる浮軽水を
ピペットで採取し、この重量し)をブリージング量とす
る。
Slurry 1 immediately after mixing into a 1000ml graduated cylinder
After filling with 0100O, the floating light water generated for 30 minutes was collected with a pipette, and the weight was taken as the breathing amount.

五)ユニル重 ブリージング測定時に全重量を測定して求めた。5) Unil Heavy This was determined by measuring the total weight during the breathing measurement.

フロー値(流動性) 内径5望、高さ5 +、 1 cmのポリ塩化ビニル製
円筒(容量100+nl)にスラリーを充填し、その円
筒をすばやく例外上げたとぎの2分後のスラリーの広が
りの直角二方向の直径を測定し、その平均値を70−値
とする。
Flow value (fluidity) A polyvinyl chloride cylinder (capacity 100+ nl) with an inner diameter of 5mm, a height of 5mm, and 1cm is filled with slurry, and the cylinder is quickly lifted up, and the spread of the slurry after 2 minutes is measured. Measure the diameters in two directions at right angles, and take the average value as the 70-value.

ス泗狙ム施庶 pc版(500mmX 500mII+X 50n+n
+)上の高さ30mm内法−辺500IIII11の枠
内にスラリーを流し込んで室温で3日問静置した後、室
温でさらに25日間静置する。
PC version (500mmX 500mII+X 50n+n
+) After pouring the slurry into a frame with a height of 30 mm above and a side of 500III11 and allowing it to stand at room temperature for 3 days, it was allowed to stand at room temperature for an additional 25 days.

表面引張り強度は、佐久間式表面強度試験磯を用いてそ
れぞれ流し込み後3日および28日後に測定する。すな
わち、直径100IIIIIlの鋼鉄製のアタッチメン
ト3または5個をエポキシ樹脂で接着し、それぞれの引
トはがしに要する応力を測定し平均をとる。
The surface tensile strength is measured 3 days and 28 days after pouring, respectively, using a Sakuma type surface strength test rock. That is, three or five steel attachments each having a diameter of 100IIII are bonded together with epoxy resin, and the stress required for each peeling is measured and averaged.

圧縮強゛および曲げ 内法長さ16oITIII1幅40alI11深さ40
IIIIIlのJISR5201三連型枠にスラリーを
流し込み、室温で3日間静置した後、固化した石膏組成
物を取り出し、さらに室温で25日間静置して供試体と
する。
Compressive strength and internal bending length 16oITIII1 width 40alI11 depth 40
The slurry is poured into a triple JISR5201 formwork of III, and left to stand for 3 days at room temperature, and then the solidified gypsum composition is taken out and left to stand at room temperature for 25 days to prepare a specimen.

曲げ強度は、ミバエリス試験機を用いて測定した。2箇
のロール(直径8IIIII+)開のスパンを1001
11mとし、その上に供試体を上下そのままにして置き
、スパンの中央に1箇のロール(直径8IIII11)
により荷重をかけて最大荷重を求める。曲げ強度は、次
式で求める: 曲げ強度(kg/cIIlす=0,234X最大荷重(
kg)測定は、3回行ない平均をとる。
The bending strength was measured using a Michaelis tester. 2 rolls (diameter 8III+) open span 1001
11m, and place the specimen vertically on top of it, and place one roll (diameter 8III11) in the center of the span.
Find the maximum load by applying the load. The bending strength is determined by the following formula: Bending strength (kg/cIIl = 0,234 x maximum load (
kg) The measurement is performed three times and the average is taken.

圧縮強度は、曲げ強度の測定後、水平面上に置いた試供
体の折片の上面から、−辺40帥の正方形の圧力板で圧
するように最大容量20トンの圧縮強度試験機を用いて
平均毎秒80kgの加圧速度で圧砕して、最大荷重を測
定し、次式により圧縮強度を算出する: 測定は、6回行ない平均をとる。
After measuring the bending strength, the compressive strength was averaged using a compressive strength testing machine with a maximum capacity of 20 tons, using a square pressure plate with a side of 40 squares to press the top surface of the folded piece of the sample placed on a horizontal surface. The maximum load is measured by crushing at a pressurization rate of 80 kg per second, and the compressive strength is calculated using the following formula: The measurement is performed six times and the average is taken.

璽木雅 水に浸漬した供試体の曲げ強度および圧縮強度を求め、
これを浸漬していないものと比較して評価する。浸漬条
件は、流し込み後21日の供試体をさらに7日間水(2
0±3℃)に浸漬する条件である。
Determine the bending strength and compressive strength of the specimen immersed in Akimasui,
Evaluate this by comparing it with one that has not been immersed. The immersion conditions were as follows: 21 days after pouring, the specimen was soaked in water (2
0±3°C).

耐摩耗性 ティパ一式ロータリーアブレッサー(株式会社東洋精機
製作所製)で測定した。
Abrasion resistance was measured using a rotary abrasion set of Tipa (manufactured by Toyo Seiki Seisakusho Co., Ltd.).

供試体は、直径10cn+、厚さ1.30IIlの円盤
形の成型体で、室温で28日問養生したものである。
The specimen was a disc-shaped molded body with a diameter of 10 cn+ and a thickness of 1.30 IIl, which was cured at room temperature for 28 days.

次の条件で摩耗減量を秤量し、摩耗帯面積当りの摩耗量
(mg/cm2)を求める。測定値は、3回行なった平
均値である。
Weigh the wear loss under the following conditions and determine the wear amount (mg/cm2) per wear zone area. The measured value is the average value of three measurements.

回転摩耗輪:        H−22回転速度:  
       70rpm回転数=         
200回 荷重:          iooog実施例1〜2お
よび比較例1〜4 次の組成物に対して混和材を種々変えて加えて得られた
組成物に、フロー値が195±1011IIIlとなる
ように水を加えてスラリーを形成し、攪拌しながら所定
の成形型に流し込んで、それぞれ試供体を製造した。
Rotating wear wheel: H-22 rotation speed:
70 rpm rotation speed =
200 times loading: iooog Examples 1 to 2 and Comparative Examples 1 to 4 Water was added to the compositions obtained by adding various admixtures to the following compositions so that the flow value was 195 ± 1011III1. In addition, a slurry was formed and poured into a predetermined mold while stirring to produce a sample.

第1表 それぞれの試供体について測定した特性を第4表に示す
Table 4 shows the characteristics measured for each sample in Table 1.

実施例3および比較例5 次のi酸物において高炉セメントの量を種々変ように水
を加えてスラリーを形成し、攪拌しながら所定の成形型
に流し込んで、それぞれ試供体を製造した。
Example 3 and Comparative Example 5 Using the following i-acid, various amounts of blast furnace cement were added with water to form a slurry, and the slurry was poured into a predetermined mold while being stirred to produce a sample.

第2表 それぞれについて測定した特性を第4表に示す。Table 2 Table 4 shows the properties measured for each.

実施例4 次の組成物にフロー値が195±10 +0+0と・な
るように水を加えてスラリーを形成し、攪拌しながら所
定の成形型に流し込んで、それぞれ試供体を製造した。
Example 4 Water was added to the following compositions to give a flow value of 195±10 +0+0 to form a slurry, and the slurry was poured into a predetermined mold while stirring to produce sample specimens.

第3表 それぞれについて測定した特性を第4表に示す。Table 3 Table 4 shows the properties measured for each.

手  続  補  正  書  (自発)昭和57年特
許願第100994号 5、補正命令の日付: (自 発) 6、補正の対象二   明細書の「発明の詳細な説明」
の欄?、補正の内容 明細書の発明の詳細な説明の欄中、次の箇所を補正しま
す。
Procedural amendment (voluntary) Patent Application No. 100994 of 1982 5. Date of amendment order: (voluntary) 6. Subject of amendment 2. “Detailed description of the invention” in the specification
column? , Contents of the amendment The following sections will be amended in the detailed description of the invention in the specification.

(1)11頁第1表第8欄、12頁第2表第8欄および
13頁第3表第8欄、「シリコン消泡剤」とあるを「消
泡剤」と訂正。
(1) In Column 8 of Table 1 on page 11, Column 8 of Table 2 on page 12, and Column 8 of Table 3 on page 13, "silicone antifoaming agent" was corrected to "antifoaming agent."

(2)13頁末行の次に、[なお、比較例2における3
日後の表面強度は、表面硬化不良のrこめ測定できなか
った。また、比較例2における耐水性は、硬化体強度が
曲げも圧縮も池のものに比べ明らかに小であるため測定
しなかった。]を挿入。
(2) Next to the last line of page 13, [Note that 3 in Comparative Example 2
The surface strength after several days could not be measured due to poor surface hardening. Furthermore, the water resistance in Comparative Example 2 was not measured because the strength of the cured product was clearly lower than that of the cured product in both bending and compression. ] Insert.

以上that's all

Claims (1)

【特許請求の範囲】 1、(a)11型無水石膏150重量部、(b)高炉上
メン)A種または8種75〜175重量部および(c)
硬化促進剤0.75〜7.5重量部を含んで成る流し延
べ床材用II型無水石膏組成物。 2、 (a)II型無水石膏150重量部、(b)高炉
セメン)A種または8種75〜175重量部および(c
)硬化促進剤0.75〜7.51重量部を含んで成るI
I型無水石膏組成物、骨材および要すれば他の添加物の
1種またはそれ以上を水と混合し、下地床に流布し、硬
化させることを特徴とする流し延、べ床材の施工法。
[Claims] 1. (a) 150 parts by weight of type 11 anhydrite, (b) 75 to 175 parts by weight of type A or type 8 (blast furnace top), and (c)
A type II anhydrite composition for cast flooring comprising 0.75 to 7.5 parts by weight of a hardening accelerator. 2. (a) 150 parts by weight of type II anhydrite, (b) blast furnace cement) 75 to 175 parts by weight of type A or type 8, and (c
) I comprising 0.75 to 7.51 parts by weight of a curing accelerator.
Construction of cast and bed flooring materials, characterized in that one or more of the type I anhydrite compositions, aggregates and optionally other additives are mixed with water, spread on the subfloor and allowed to harden. Law.
JP10099482A 1982-06-11 1982-06-11 Anhydrous gypsum composition for flow-spread floor material and construction therefor Granted JPS58217455A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10099482A JPS58217455A (en) 1982-06-11 1982-06-11 Anhydrous gypsum composition for flow-spread floor material and construction therefor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10099482A JPS58217455A (en) 1982-06-11 1982-06-11 Anhydrous gypsum composition for flow-spread floor material and construction therefor

Publications (2)

Publication Number Publication Date
JPS58217455A true JPS58217455A (en) 1983-12-17
JPS6346022B2 JPS6346022B2 (en) 1988-09-13

Family

ID=14288854

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10099482A Granted JPS58217455A (en) 1982-06-11 1982-06-11 Anhydrous gypsum composition for flow-spread floor material and construction therefor

Country Status (1)

Country Link
JP (1) JPS58217455A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61155242A (en) * 1984-12-26 1986-07-14 大阪セメント株式会社 Water-resistant fluoric anhydrous gypsum composition
EP0208535A1 (en) * 1985-07-12 1987-01-14 SHIMIZU CONSTRUCTION Co. LTD. Process of producing a flowing concrete
JPS62191455A (en) * 1986-02-19 1987-08-21 浅野スレ−ト株式会社 Anhydrous gypsum papered board and manufacture
EP0916627A1 (en) * 1997-11-17 1999-05-19 Al Kassem, Nizar Additive for binder used in the building industry and material containing the same

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61155242A (en) * 1984-12-26 1986-07-14 大阪セメント株式会社 Water-resistant fluoric anhydrous gypsum composition
EP0208535A1 (en) * 1985-07-12 1987-01-14 SHIMIZU CONSTRUCTION Co. LTD. Process of producing a flowing concrete
JPS62191455A (en) * 1986-02-19 1987-08-21 浅野スレ−ト株式会社 Anhydrous gypsum papered board and manufacture
JPH0566895B2 (en) * 1986-02-19 1993-09-22 Asano Slate Co Ltd
EP0916627A1 (en) * 1997-11-17 1999-05-19 Al Kassem, Nizar Additive for binder used in the building industry and material containing the same
FR2771087A1 (en) * 1997-11-17 1999-05-21 Kassem Nizar Al ADJUVANT FOR BINDER USED IN CONSTRUCTION, AND MATERIAL COMPRISING SAME

Also Published As

Publication number Publication date
JPS6346022B2 (en) 1988-09-13

Similar Documents

Publication Publication Date Title
CN109400076A (en) A kind of strong concrete and its preparation process
Punkki et al. Workability loss of high-strength concrete
CN108424073A (en) A kind of high abrasion high-strength concrete and preparation method thereof
US5250113A (en) Dry castable concrete compositions and methods of preparing and dry casting the same
CN111548094A (en) Impervious concrete and proportioning method thereof
CN110903065A (en) Quick-setting 3D printing cement-based material
Benabed et al. Effect of limestone powder as a partial replacement of crushed quarry sand on properties of self-compacting repair mortars
KR101052602B1 (en) High performance floor mortar composition using fluidizing compound and method for preparing same
JPH0345544A (en) Concrete blend composition
JP4181224B2 (en) Cement composition and concrete and concrete product manufacturing method using the same
JPS58217455A (en) Anhydrous gypsum composition for flow-spread floor material and construction therefor
JP5403496B2 (en) Hardened concrete and concrete composition
JP4691423B2 (en) Centrifugal forming material and method for producing centrifugal formed concrete product
Esping et al. Investigation of early age deformation in self-compacting concrete
JP2701028B2 (en) Cement-based self-leveling material
JPH0753248A (en) Cement admixture and cement composition
JP2567322B2 (en) Highly Fillable Fresh Concrete for Cast-in-Place
JPH0520378B2 (en)
JP2510870B2 (en) Construction method of self-leveling material
JP2018119922A (en) Consistency test method for cement composition
JPS6230652A (en) Machine member and tool
JP3026406B2 (en) Manufacturing method and construction method of self-smoothing cement mortar composition
GEBEYEHU OPTIMIZATION OF SUPERPLASTICIZER DOSAGE AND EFFECTS WITH LOCALLY PRODUCED CEMENTS ON READY-MIX CONCRETE PROPERTIES
JP3875028B2 (en) Manufacturing method of centrifugal molded products
JP2002137952A (en) Hydraulic composition