JPH01119551A - Cement admixture - Google Patents
Cement admixtureInfo
- Publication number
- JPH01119551A JPH01119551A JP27574487A JP27574487A JPH01119551A JP H01119551 A JPH01119551 A JP H01119551A JP 27574487 A JP27574487 A JP 27574487A JP 27574487 A JP27574487 A JP 27574487A JP H01119551 A JPH01119551 A JP H01119551A
- Authority
- JP
- Japan
- Prior art keywords
- sulfate
- cement
- admixture
- alkali metal
- defoaming agent
- 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
Links
- 239000004568 cement Substances 0.000 title claims abstract description 27
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 13
- 229910052936 alkali metal sulfate Inorganic materials 0.000 claims abstract description 9
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims abstract description 9
- 239000004570 mortar (masonry) Substances 0.000 abstract description 11
- 239000000203 mixture Substances 0.000 abstract description 7
- 229920001296 polysiloxane Polymers 0.000 abstract description 5
- 238000002156 mixing Methods 0.000 abstract description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 abstract description 2
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 abstract description 2
- 229910052939 potassium sulfate Inorganic materials 0.000 abstract description 2
- 235000011151 potassium sulphates Nutrition 0.000 abstract description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 abstract description 2
- 235000011152 sodium sulphate Nutrition 0.000 abstract description 2
- 230000008961 swelling Effects 0.000 abstract 2
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 238000005336 cracking Methods 0.000 abstract 1
- 238000004227 thermal cracking Methods 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000011398 Portland cement Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000009415 formwork Methods 0.000 description 3
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- -1 fatty acid ester Chemical class 0.000 description 2
- 239000010881 fly ash Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 1
- 208000035484 Cellulite Diseases 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 206010049752 Peau d'orange Diseases 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000003254 anti-foaming effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000036232 cellulite Effects 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、セメント混和材、特に硫酸アルミニ9ムとア
ルカリ金属硫酸塩及び消泡剤からなる、高い早期強度を
発現するセメント混和材に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a cement admixture, and particularly to a cement admixture that exhibits high early strength and is composed of aluminum sulfate, an alkali metal sulfate, and an antifoaming agent.
く従来の技術とその問題点〉
従来、早期強度の高いセメント硬化体を製造する方法と
しては、セメントに硫酸アルミニウム及びシリカ糸化合
物粒子等からなる混和剤を配合し紡養生を必要とせず、
直ちに昇温し、高温養生する方法が提案された(%開昭
62−52158号公報)。Conventional techniques and their problems> Conventionally, as a method for producing hardened cement with high early strength, cement is mixed with an admixture consisting of aluminum sulfate and silica thread compound particles, etc., without the need for spinning and curing.
A method was proposed in which the temperature was raised immediately and the material was cured at a high temperature (Patent Publication No. 52158/1983).
しかしながらこの方法はコンクリートの凝結が早い、作
業性が悪い等実用上問題が大きく、又養生後の脱型強度
の面でも充分なものではなく、熱によシフラック及びフ
クレ等の発生があシ、外観上優れたものではなかった。However, this method has many practical problems such as rapid setting of concrete and poor workability.Also, the strength of demolding after curing is not sufficient, and sagging and blistering may occur due to heat. It wasn't visually appealing.
本発明者らは、上記問題点を解消すべく種々検討した結
果、硫酸アルミニウムとアルカリ金属硫酸塩と消泡剤と
を主成分とするセメント混和材を用いることによシ、一
定の作業性を有し、短時間の高温養生によシ数時間で型
枠脱温に必要な強度を発現せしめ、クラックや7クレ等
のない外観の優れたセメント硬化体が出来る知見を得て
、本発明を完成するに到った。As a result of various studies to solve the above problems, the present inventors have found that a certain level of workability can be achieved by using a cement admixture whose main components are aluminum sulfate, alkali metal sulfate, and an antifoaming agent. The present invention was developed based on the knowledge that a hardened cement product with excellent appearance without cracks or cracks, etc. can be obtained by developing the strength necessary for dewarming the formwork in a few hours by short-term high-temperature curing. It has been completed.
く問題点を解決するための手段〉
即ち、本発明は硫酸アルミニウム、アルカリ金属硫酸塩
及び消泡剤からなるセメント混和材である。Means for Solving the Problems> That is, the present invention is a cement admixture comprising aluminum sulfate, an alkali metal sulfate, and an antifoaming agent.
以下本発明の詳細な説明する。The present invention will be explained in detail below.
本発明に係るセメントとしては、普通・早強・超早強等
の各種ポルトランドセメントや、島炉スラグやフライア
ッシュ等を混合した各種混合セメント等いずれのセメン
トの使用も可能である。As the cement according to the present invention, any cement can be used, such as various types of Portland cement such as normal, early strength, and super early strength, and various mixed cements mixed with island furnace slag, fly ash, etc.
硫酸アルミニウム(以下硫酸)lという)としては無水
物あるいは水和物、例えば、
Al2(SO4)3・12〜18H20、のいずれのも
のでも使用でき、粉末あるいは水溶液として使用できる
。The aluminum sulfate (hereinafter referred to as sulfuric acid) can be either anhydrous or hydrated, such as Al2(SO4)3.12-18H20, and can be used as a powder or an aqueous solution.
粉末状のときは、特に微粉、例えば、100メツシユ以
下のほうが好ましい。When it is in powder form, it is particularly preferable to use fine powder, for example, 100 mesh or less.
アルカリ金属硫酸塩(以下硫酸アルカリという)は硫酸
ナトリクム(以下硫酸Naという)及び/又は硫酸カリ
ウム(以下硫酸にという)で通常のものが使用できるが
、作業性及び強度発現の面から硫rRNaが好ましい。As the alkali metal sulfate (hereinafter referred to as alkali sulfate), ordinary sodium sulfate (hereinafter referred to as Na sulfate) and/or potassium sulfate (hereinafter referred to as sulfuric acid) can be used, but from the viewpoint of workability and strength development, sulfur rRNa is preferable. preferable.
硫酸アルカリの使用量は、硫酸AJ1001に置部に対
し、硫酸アルカリ50〜300Xji部、好ましくは7
0〜200!量部、特に好ましくは80〜150重量部
である。501景部未満であると、セメ・ント混練物の
凝結速度が早く、作業性が収れないはか9か、強度増進
効果が少ない。300!31部を越えると、短期強度発
現が急くなる。The amount of alkali sulfate used is 50 to 300Xji parts, preferably 7 parts per part of sulfuric acid AJ1001.
0-200! Parts by weight, particularly preferably 80 to 150 parts by weight. If it is less than 501 parts, the solidification rate of the cement mixture will be fast, the workability will be poor, and the strength-enhancing effect will be small. When exceeding 300!31 parts, short-term strength development becomes rapid.
消泡剤としてはシリコーン系、ノニオン系、アルコール
、脂肪酸、エーテル、脂肪酸エステル、リン酸エステル
や、ポリエーテル系、フッ素系などがあげられる。Examples of antifoaming agents include silicone type, nonionic type, alcohol, fatty acid, ether, fatty acid ester, phosphoric acid ester, polyether type, and fluorine type.
具体的には、シリコーン系はオイル型及びそのオイル型
をトルエン等の溶剤で溶かした溶液型、又、シリコーン
オイルに無機質の微粉末を添加し。Specifically, silicone-based products include an oil type, a solution type in which the oil type is dissolved in a solvent such as toluene, and a silicone type in which fine inorganic powder is added to silicone oil.
たコンパウンド製、更には各種の乳化剤を用いたエマル
ジョン童吟が挙げられる。消泡剤とし℃は消泡効果及び
モルタル硬化体表面性状の面から、シリコーン系及びノ
ニオン系が好ましい。Examples include emulsion dogin made from a compound made with a sulfuric acid compound, and emulsion dogin made using various emulsifiers. As the antifoaming agent, from the viewpoint of antifoaming effect and surface properties of the cured mortar, silicone-based and nonionic anti-foaming agents are preferable.
消泡剤はセメント混練物の凝結前の高温養生を可能とし
、高温養生後のコンクリート表面のクラックを防止し、
更には強度増進及びセメント硬化体の表面性状を向上さ
せるため必要なものである。Antifoaming agents enable high-temperature curing of cement mixtures before setting, and prevent cracks on the concrete surface after high-temperature curing.
Furthermore, it is necessary for increasing the strength and improving the surface quality of the hardened cement body.
その消泡剤の使用量は、@酸AJ1!:m酸アルカリの
混合物1001量部に対し、0.1〜6″X童部が好ま
しく、0.3〜2重量部が更に好ましい。0.1]Li
i部未満であると、上記効果がなくなシ、3重量部を越
えても効果は変らず経済的でない。The amount of antifoaming agent used is @acid AJ1! : 0.1 to 6" x parts is preferable, more preferably 0.3 to 2 parts by weight, per 1001 parts by weight of the m-acid alkali mixture. 0.1] Li
If the amount is less than i part, the above effects will be lost, and if it exceeds 3 parts by weight, the effect will not change and it is not economical.
混和材の使用量は、セメント1oox量部に対し、混和
材2〜103(置部が好ましく、6〜71量部が更に好
ましい。2重量部未満であると、高温養生後のコンクリ
ート表面にクラックの発生する恐れが生じ、強度発現が
急く、10重製部を越えても強度増進の効果は少なく経
済的でない。The amount of admixture used is 2 to 103 parts (preferably 6 to 71 parts by weight, more preferably 6 to 71 parts by weight) per 100 parts of cement. If it is less than 2 parts by weight, cracks may occur on the concrete surface after high temperature curing. There is a risk that this will occur, and the strength will develop quickly.Even if the number of parts exceeds 10, the effect of increasing strength will be small and it will not be economical.
混和材の混合方法は、1)あらかじめセメントと混合す
る。 2)モルタルやコンクリートcD混11時に混合
する。 3)モルタルやコンクリート混練)後任意の時
間、例えば、1時間以内に添加する。The method of mixing the admixture is as follows: 1) Mix it with cement in advance. 2) Mix mortar and concrete cD at 11 o'clock. 3) Add at any time after (mixing mortar or concrete), for example, within 1 hour.
4)水浴液にし混合する等いずれの方法でも実施可能で
ある。尚、混和材は各材料を同時に混合してもよく、別
々に混合してもよい。4) Any method can be used, such as mixing in a water bath solution. In addition, each material may be mixed simultaneously or separately as an admixture.
更に必要に応じ、一般市販のセメント減水剤、例エバ、
β−ナフタレンスルホン[J[ホルマリン縮合物、メラ
ミンスルホン酸塩等使用することによシそれ相当の効果
がある。Furthermore, if necessary, commercially available cement water reducers, such as Eva,
The use of β-naphthalene sulfone [J[formalin condensate, melamine sulfonate, etc.] has corresponding effects.
本発明の混和材を用いる場合、凝結調節剤としてホシ酸
、リン酸及びケイ弗化物あるいはその塩などの無機化合
物、又はクエン酸、酒石酸及びグルコン酸などのオヤシ
ヵルボン酸あるいはその塩などを使用することができる
。When using the admixture of the present invention, inorganic compounds such as phosic acid, phosphoric acid, and silicofluorides or salts thereof, or oxycarboxylic acids or salts thereof such as citric acid, tartaric acid, and gluconic acid may be used as setting regulators. Can be done.
更にシリカフラワー、フライアッシュ及び微粉高炉スラ
グ等を使用することにょシセメント硬化体の外観面の状
態を改良できる。Furthermore, the appearance of the hardened cement can be improved by using silica flour, fly ash, pulverized blast furnace slag, etc.
セメントペースト、モルタル及びコンクリート(以下コ
ンクリート類という)の成形方法としては、型枠に打設
するか又は遠心成形などいずれでもよい。Cement paste, mortar, and concrete (hereinafter referred to as concrete) may be formed by either casting in a formwork or centrifugal forming.
こうして成形されたコンクリート類は、常温で直ちに、
好ましくは20分以上の前養生を行なった後、昇温を行
なう。昇温速度は型枠の転用回数を考慮し、20〜b
〜60°C/時間が良く、昇温速度がこの範囲よシ早い
とコンクリート表面に熱応力クラックが発生しやすい。The concrete formed in this way is immediately heated at room temperature.
Preferably, after pre-curing for 20 minutes or more, the temperature is increased. The temperature increase rate should be 20 to 60°C/hour, taking into account the number of times the formwork will be used. If the temperature increase rate is faster than this range, thermal stress cracks are likely to occur on the concrete surface.
養生の保持温度は(ピーク温度)50℃以上、好ましく
は60〜90℃であり、ピーク温度の養生時間は30〜
90分間保持すればよい。The holding temperature for curing is (peak temperature) 50°C or higher, preferably 60-90°C, and the curing time at peak temperature is 30-90°C.
It is sufficient to hold it for 90 minutes.
加熱手段としては電気、温風、赤外線及び蒸気等のいず
れも使用できるが蒸気養生が強度発現の点から好ましい
。As a heating means, any of electricity, hot air, infrared rays, steam, etc. can be used, but steam curing is preferable from the viewpoint of developing strength.
セメント硬化体は上記の高温養生後、直ちに脱型され、
全1の工程が終了する。After the hardened cement body is cured at the above-mentioned high temperature, it is immediately removed from the mold.
All 1 process is completed.
このようKして短時間で得られたセメント硬化体は普通
ポルトランドセメントのみを使用したセメント硬化体に
比べ、外観が優れ、耐久性においてもなんら変ることが
ない。A hardened cement body obtained in a short time by such K treatment has a superior appearance and no change in durability compared to a hardened cement body using only ordinary Portland cement.
〈実施例〉 次に実施例をあけC更に本発明を説明する。<Example> Next, the present invention will be further explained with reference to Examples.
実施例1
普通ポルトランドセメント100重皿部(電気化学社製
)、細骨材(姫用産砂、FM=2.7)200重量部、
セメント減水剤(花王社製商品名「マイティ100」
)0.51蓋部、水433に置部、表−1に示す混和材
5重波部からなるモルタルをJIS R5201に準じ
て混練し、モルタル供試体(4x4x16cm)を作シ
、20分後熟気養生を開始した。昇温速度は40℃/時
間で80℃になった時点で30分間保持し、その後すぐ
に脱型した。コンクリートの外観状態を観察し3時間、
1日、28日の圧縮強度を測定した。史に実験隘6と8
のモルタルを20°C−80RH室で養生したものにつ
いても同様の試験を行った。結果t−1−2に示す。Example 1 100 parts by weight of ordinary Portland cement (manufactured by Denki Kagaku Co., Ltd.), 200 parts by weight of fine aggregate (sand for Hime, FM=2.7),
Cement water reducer (product name: “Mighty 100” manufactured by Kao Corporation)
) A mortar consisting of a 0.51 lid part, a part placed in water 433, and 5 double wave parts of the admixture shown in Table 1 was kneaded according to JIS R5201, a mortar specimen (4 x 4 x 16 cm) was prepared, and it was aged for 20 minutes. I started taking care of myself. The temperature was raised at a rate of 40° C./hour, and when the temperature reached 80° C., it was held for 30 minutes, and the mold was demolded immediately thereafter. Observing the external appearance of concrete for 3 hours,
The compressive strength was measured on the 1st and 28th day. Experiments in history 6 and 8
A similar test was also conducted on mortar cured in a 20°C-80RH room. The results are shown in t-1-2.
宍−2
実験−16及び17は各々、実験−6及び8のモルタル
使用
実験−18は混和材無し
H,T :ハンドリングタイム
実施例2
実験−7の配合の混和材のtt−変えたこと以外は実施
例1と同様に行った。結果を衣−3に示す。Shishi-2 Experiments-16 and 17 use mortar in Experiments-6 and 8, respectively.Experiment-18 uses no admixture H, T: Handling time Example 2 Except for changing the admixture tt in the mixture of Experiment-7. was carried out in the same manner as in Example 1. The results are shown in Cloth-3.
懺から本発明品は凝結前に蒸気養生を行なってもセルタ
ル等のクラックは発生しなく短長期の強度発現社良好で
ある。From the results, the product of the present invention does not develop cracks such as cellulite even if it is steam-cured before condensation, and exhibits good short- and long-term strength.
〈発明の効果〉
モルタル凝結前に急速蒸気養生を行なっても、熱により
クラック及びフクレ等の発生は無く、短長期強度の発現
が良いばかりかモルタル硬化体表面につや等が有シ外観
上優れている。<Effects of the invention> Even if rapid steam curing is performed before mortar condensation, no cracks or blisters occur due to heat, and not only does short-term and long-term strength develop well, but the surface of the cured mortar has gloss and is excellent in appearance. ing.
特許出願人 電気化学工業株式会社Patent applicant Denki Kagaku Kogyo Co., Ltd.
Claims (1)
なるセメント混和材。Cement admixture consisting of aluminum sulfate, alkali metal sulfate and antifoaming agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27574487A JP2556531B2 (en) | 1987-11-02 | 1987-11-02 | Cement admixture |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27574487A JP2556531B2 (en) | 1987-11-02 | 1987-11-02 | Cement admixture |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01119551A true JPH01119551A (en) | 1989-05-11 |
JP2556531B2 JP2556531B2 (en) | 1996-11-20 |
Family
ID=17559791
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27574487A Expired - Fee Related JP2556531B2 (en) | 1987-11-02 | 1987-11-02 | Cement admixture |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2556531B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8025333B2 (en) | 2007-12-25 | 2011-09-27 | Toyota Boshoku Kabushiki Kaisha | Vehicle seats and detachable cover therefor |
-
1987
- 1987-11-02 JP JP27574487A patent/JP2556531B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8025333B2 (en) | 2007-12-25 | 2011-09-27 | Toyota Boshoku Kabushiki Kaisha | Vehicle seats and detachable cover therefor |
Also Published As
Publication number | Publication date |
---|---|
JP2556531B2 (en) | 1996-11-20 |
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