JPH0645492B2 - Admixture for concrete and mortar - Google Patents

Admixture for concrete and mortar

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Publication number
JPH0645492B2
JPH0645492B2 JP2923685A JP2923685A JPH0645492B2 JP H0645492 B2 JPH0645492 B2 JP H0645492B2 JP 2923685 A JP2923685 A JP 2923685A JP 2923685 A JP2923685 A JP 2923685A JP H0645492 B2 JPH0645492 B2 JP H0645492B2
Authority
JP
Japan
Prior art keywords
admixture
concrete
acid
general formula
mortar
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 - Lifetime
Application number
JP2923685A
Other languages
Japanese (ja)
Other versions
JPS61191547A (en
Inventor
明 田中
好伸 中村
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.)
Toho Chemical Industry Co Ltd
Original Assignee
Toho Chemical Industry 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 Toho Chemical Industry Co Ltd filed Critical Toho Chemical Industry Co Ltd
Priority to JP2923685A priority Critical patent/JPH0645492B2/en
Publication of JPS61191547A publication Critical patent/JPS61191547A/en
Publication of JPH0645492B2 publication Critical patent/JPH0645492B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Description

【発明の詳細な説明】 本発明はコンクリート用混和剤に関するものであり更に
詳しくは硬化コンクリートが気温の変化により生ずる凍
結融解の繰り返し作用によるひびわれ崩壊などの凍害を
防ぐために多数の独立した微細な空気泡をコンクリート
中に連行させたコンクリートもしくはモルタルを製造す
る目的で使用されるAE剤に係るものである。
The present invention relates to an admixture for concrete, and more specifically, to prevent freezing damage such as crack collapse by repeated action of freezing and thawing caused by changes in temperature of hardened concrete. It relates to an AE agent used for the purpose of producing concrete or mortar in which bubbles are entrained in concrete.

AE剤として広く知られているものに天然樹脂酸塩,ア
ルキルサルフェート,あるいはアルキルアリルスルホン
酸塩、などの陰イオン系の界面活性剤,あるいは、ポリ
オキシエチレンアルキルアリールエーテルなどの非イオ
ン界面活性剤が知られている。その作用はセメント粒子
や細骨材の間隙にある空気と水の界面に吸着し、その界
面活性作用によって微細な独立気泡をコンクリート中に
均一に分布させ、気泡のベアリング効果によって流動性
を付与し、作業性を改善すると共に寒冷地における路面
舗装などの凍害をうけた場合コンクリート中に分布した
微細な独立気泡が自由水の凍結によって生じる大きな体
積膨張圧を緩和し、コンクリートのひび割れひいては破
壊に対する抵抗性を付与することにある。
Widely known AE agents include anionic surfactants such as natural resin salts, alkyl sulfates, and alkylallyl sulfonates, or nonionic surfactants such as polyoxyethylene alkylaryl ethers. It has been known. Its action is that it is adsorbed at the interface between air and water in the gaps between cement particles and fine aggregates, and its surface-active action causes fine closed cells to be evenly distributed in the concrete, and imparts fluidity by the bearing effect of the bubbles. Improves workability, and when subjected to frost damage such as road surface pavement in cold regions, the fine closed cells distributed in the concrete alleviate the large volume expansion pressure caused by freezing of free water, and resist cracking and destruction of concrete. To impart sex.

しかし、従来から使用されているAE剤は、その種類に
よって、連行された気泡の大きさ、あるいは気泡の分布
状態がかなり異っていることは周知のことである。即ち
樹脂酸塩系は、微細な独立気泡は得られるが、耐硬水性
に欠け硬度の高い水には使用出来ない。アルキルサルフ
ェートなど陰イオン系のものは気泡が軟らかく、又、非
イオン系のものは泡の粒径が大きくなるため泡の安定性
が劣り、AE剤としての効果も小さいなどそれぞれの欠
点を有している。従って、使用に際しては使用条件によ
ってそれぞれ使い分けているのが現状である。
However, it is well known that conventionally used AE agents have considerably different sizes of entrained bubbles or distribution states of bubbles depending on the type. That is, the resin acid salt system can obtain fine closed cells, but cannot be used for water having a high hardness and lacking hard water resistance. Anion type such as alkyl sulphate has soft air bubbles, and non-ionic type has large foam particle size, so that foam stability is poor and effect as AE agent is small. ing. Therefore, it is the current situation that they are used properly depending on the usage conditions.

本発明者らは、かかる現状での欠点を解決すべく鋭意検
討の結果本発明の界面活性剤がAE剤として優れた性能
を有することを見い出した。
The inventors of the present invention have found that the surfactant of the present invention has excellent performance as an AE agent as a result of intensive studies to solve the above-mentioned drawbacks.

即ち、本発明は、 (1)下記一般式 (但し、Aは3〜6個のOH基を有する多価アルコール
残基,Rは炭素数6〜22の高級脂肪酸残基を示す。
That is, the present invention is (1) the following general formula (However, A represents a polyhydric alcohol residue having 3 to 6 OH groups, and R represents a higher fatty acid residue having 6 to 22 carbon atoms.

1+m+nは1〜100の整数であり、X及びZは1〜
5の整数、Yは0もしくは1〜4の整数でかつ、X,
Y,Zの総数はAの有するOH基の数に相当することを
示す。またMはアルカル金属,アンモニウム,もしくは
炭素数6以下のN−アルキル(又はアルカノール)アン
モニウムを示す。)を含有することを特徴とするコンク
リート及びモルタル用混和剤。
1 + m + n is an integer of 1 to 100, and X and Z are 1 to
An integer of 5, Y is 0 or an integer of 1 to 4, and X,
It is shown that the total number of Y and Z corresponds to the number of OH groups possessed by A. Further, M represents an alcal metal, ammonium, or N-alkyl (or alkanol) ammonium having 6 or less carbon atoms. And an admixture for concrete and mortar.

(2)一般式において、Aがソルビット残基である特許請
求範囲第(1)項記載の混和剤。
(2) The admixture according to claim (1), wherein A is a sorbit residue in the general formula.

(3)一般式に於て、Rがオレイン酸残基である特許請求
範囲第(1)項及び第(2)項記載の混和剤。
(3) The admixture according to claims (1) and (2), wherein R in the general formula is an oleic acid residue.

(4)一般式に於て、1+m+nが30〜60の整数であ
る特許請求範囲第(1)項,第(2)項及び第(3)項
記載の混和剤に係るものである。
(4) In the general formula, 1 + m + n is an integer of 30 to 60, and relates to the admixture according to claims (1), (2) and (3).

本発明の化合物は公知の方法にて容易に得られる。即
ち、多価アルコール例えば、グリセリン,ペンタエリス
リトール,ジグリセリン,アラビット,ソルビット,マ
ンニット及びジペンタエリスリトール等から選ばれた多
価アルコールに水酸化アルカリ触媒を用いて、酸化エチ
レン(以下EOという)を付加反応させ、次いで酸又
は、アルカリ触媒を用いて、高級脂肪酸、例えば、カプ
ロン酸,カプリル酸,カプリン酸,ラウリン酸,ミリス
チン酸,パルミチン酸,オレイン酸,ステアリン酸及び
ベヘニン酸等から選ばれた高級脂肪酸との部分エステル
化反応を行ない、その後に残存するOH基を当量の硫酸
化剤例えば、硫酸,クロルスルホン酸,無水硫酸,スル
ファミン酸等から選ばれたものにて硫酸化すればよい。
The compound of the present invention can be easily obtained by a known method. That is, polyhydric alcohols, for example, polyhydric alcohols selected from glycerin, pentaerythritol, diglycerin, arabite, sorbit, mannite, dipentaerythritol and the like are treated with an alkali hydroxide catalyst to give ethylene oxide (hereinafter referred to as EO). Addition reaction and then acid or alkali catalyst is used to select higher fatty acid such as caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, oleic acid, stearic acid and behenic acid. A partial esterification reaction with a higher fatty acid may be carried out, and the remaining OH groups may be sulfated with an equivalent amount of a sulfating agent such as sulfuric acid, chlorosulfonic acid, sulfuric acid anhydride, sulfamic acid and the like.

しかし、経済性,有用性の面から、好ましくは、多価ア
ルコールはソルビット,EOの付加量は30〜60モル
であり,脂肪酸はオレイン酸がよい。又は、硫酸化剤と
してはスルファミン酸が好ましく他はエステル結合部分
の加水分解が起り易いので注意する必要がある。
However, from the viewpoint of economy and usefulness, it is preferable that the polyhydric alcohol is sorbit and the addition amount of EO is 30 to 60 mol, and the fatty acid is oleic acid. Alternatively, sulfamic acid is preferable as the sulfating agent, and the other is susceptible to hydrolysis of the ester bond portion, so care must be taken.

本発明に於ける化合物は、単独で使用しても微細な起泡
性と、泡の持続性を有する優れたAE剤であるが、また
他のセメント混和剤例えばセメント分散剤や高性能減水
剤等と、併用、あるいは混合して使用しても、AE剤と
しての機能を阻害されることはない。
The compound in the present invention is an excellent AE agent having a fine foaming property and a foam lasting property even when used alone, but also other cement admixtures such as a cement dispersant and a high-performance water reducing agent. Etc., the function as an AE agent is not impaired even when used in combination or in a mixture.

以下本発明によるセメント混和剤について実施例をもっ
て説明するが本発明はこれに限定されるものではない。
Hereinafter, the cement admixture according to the present invention will be described with reference to Examples, but the present invention is not limited thereto.

〔実施例〕〔Example〕

化合物製造例 1 加圧反応釜にソルビット182部(1モル)を仕込み触
媒として苛性カリ、0.5部を入れ、110〜120℃
で1時間脱水した後、反応釜を窒素置換する。
Compound Production Example 1 182 parts (1 mol) of sorbit was charged into a pressure reaction kettle, and 0.5 part of caustic potash was added as a catalyst, 110 to 120 ° C.
After dehydration for 1 hour, the reaction kettle is replaced with nitrogen.

次いで、圧力2〜3kg/cm2,温度145〜150℃で
EO1760部(40モル)を反応させた後同温で約1
時間熟成する。
Next, after reacting 1760 parts (40 mol) of EO at a pressure of 2 to 3 kg / cm 2 and a temperature of 145 to 150 ° C., the reaction temperature is about 1
Mature for hours.

反応物を四ッ口フラスコにとり、オレイン酸846部
(3モル)と苛性カリ7部を入れ、220〜230℃で
約5時間,脱水反応を行ない、反応率95%以上のエス
テル化物を得た。このものを130℃に冷却し、スルフ
ァミン酸219部(3モル)及び触媒として尿素180
部(3モル)を仕込み同温で2時間硫酸化した後、アン
モニア水でpH7〜8に調整し、本発明の混和剤(化合
物(1))を得た。
The reaction product was placed in a four-necked flask, and 846 parts (3 mols) of oleic acid and 7 parts of caustic potash were added, and dehydration reaction was carried out at 220 to 230 ° C. for about 5 hours to obtain an esterified product having a reaction rate of 95% or more. This was cooled to 130 ° C., 219 parts (3 mol) of sulfamic acid and 180 urea as a catalyst.
Part (3 mol) was charged, and the mixture was sulfated at the same temperature for 2 hours and then adjusted to pH 7 to 8 with aqueous ammonia to obtain the admixture (compound (1)) of the present invention.

化合物製造例 2〜4 化合物製造例1に準じて製造した本発明の混和剤(化合
物製造例(2)〜(4))の合成条件を表−1にまとめ
て記す。本発明の混和剤(化合物製造例(1)〜
(4))を実施例1〜3のテスト用に供する。
Compound Production Examples 2 to 4 The synthesis conditions for the admixture of the present invention (Compound Production Examples (2) to (4)) produced according to Compound Production Example 1 are summarized in Table 1. The admixture of the present invention (Compound Production Example (1)-
(4)) is used for the tests of Examples 1 to 3.

実施例 1 耐硬水性を確認するため50゜dH,100゜dH,2
00゜dHの各硬水100gに対し、混和剤0.5g,
及び0.1gを添加、溶解性を観察した。結果を表−2
に記す。
Example 1 In order to confirm hard water resistance, 50 ° dH, 100 ° dH, 2
To 100 g of each hard water of 00 ° dH, 0.5 g of the admixture,
And 0.1 g were added, and the solubility was observed. The results are shown in Table-2.
Note.

表−2にて明らかなごとく本発明の混和剤は樹脂酸系の
混和剤に比し、耐硬水性に優れていることを確認した。
As is clear from Table 2, it was confirmed that the admixture of the present invention was superior in hard water resistance to the resin acid-based admixture.

実施例 2 モルタルミキサーに普通ポルトランドセメント400g
及び細骨材(豊浦標準砂)1200gを入れ、1分間低
速回転で混合後混和剤0.02gを溶解した水240g
を加えて3分間混練したモルタルについて気泡の安定性
を測定した結果を表−3に記す。
Example 2 400 g of ordinary Portland cement in a mortar mixer
And 1200g of fine aggregate (Toyoura standard sand) was put in, and after mixing for 1 minute at low speed, 240g of water in which 0.02g of admixture was dissolved
Table 3 shows the results of measuring the stability of bubbles in a mortar obtained by adding and kneading for 3 minutes.

表−3より、一般に市販されている陰イオン系及び非イ
オン系混和剤に比較して本発明混和剤が長時間安定な泡
を保有する事が認められた。
From Table 3, it was confirmed that the admixture of the present invention possesses a foam that is stable for a long time, as compared with generally marketed anionic and nonionic admixtures.

実施例 3 下記材料を下記の測定法によってコンクリートへの空気
連行性とスランプ圧縮強度を測定した結果を表−4に示
す。
Example 3 The results of measuring the air entrainment to concrete and the slump compressive strength of the following materials by the following measuring methods are shown in Table-4.

材料 セメント……普通ポルトランドセメント(比重3.1
6) 細骨材……川砂(比重2.61) 粗骨材……川砂利(比重2.63) 測定法 スランプ JIS A 1101 空気量 JIS A 1128 圧縮強度 JIS A 1108 表−4より明らかなごとく、本発明による混和剤は低添
加量でも市販されているものに比較して優れていること
がわかる。
Material Cement ...... Normal Portland cement (specific gravity 3.1)
6) Fine aggregate …… River sand (specific gravity 2.61) Coarse aggregate …… River gravel (specific gravity 2.63) Measurement method Slump JIS A 1101 Air volume JIS A 1128 Compressive strength JIS A 1108 As is clear from Table 4, the admixture according to the present invention is superior to the admixture on the market even at a low addition amount.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】下記一般式 (但し、Aは3〜6個のOH基を有する多価アルコール
残基,Rは炭素数6〜22の高級脂肪酸残基を示す。1
+m+nは1〜100の整数であり、X及びZは1〜5
の整数、Yは0もしくは、1〜4の整数でかつX,Y,
Zの総数はAの有するOH基の数に相当することを示
す。またMはアルカリ金属,アンモニウムもしくは、炭
素数6以下のN−アルキル(又はアルカノール)アンモ
ニウムを示す)を含有することを特徴とするコンクリー
ト及びモルタル用混和剤。
1. The following general formula (However, A represents a polyhydric alcohol residue having 3 to 6 OH groups, and R represents a higher fatty acid residue having 6 to 22 carbon atoms.
+ M + n is an integer of 1 to 100, and X and Z are 1 to 5
, Y is 0 or an integer of 1 to 4 and X, Y,
It is shown that the total number of Z corresponds to the number of OH groups possessed by A. M is an admixture for concrete and mortar, which contains an alkali metal, ammonium, or N-alkyl (or alkanol) ammonium having 6 or less carbon atoms).
【請求項2】一般式においてAがソルビット残基である
特許請求範囲第(1)項記載の混和剤。
2. The admixture according to claim 1, wherein A in the general formula is a sorbit residue.
【請求項3】一般式においてRがオレイン酸残基である
特許請求範囲第(1)項及び第(2)項記載の混和剤。
3. The admixture according to claims (1) and (2), wherein R in the general formula is an oleic acid residue.
【請求項4】一般式において1+m+nが30〜60の
整数である特許請求範囲第(1)項,第(2)項及び第
(3)項記載の混和剤。
4. The admixture according to claims (1), (2) and (3), wherein 1 + m + n in the general formula is an integer of 30 to 60.
JP2923685A 1985-02-19 1985-02-19 Admixture for concrete and mortar Expired - Lifetime JPH0645492B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2923685A JPH0645492B2 (en) 1985-02-19 1985-02-19 Admixture for concrete and mortar

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2923685A JPH0645492B2 (en) 1985-02-19 1985-02-19 Admixture for concrete and mortar

Publications (2)

Publication Number Publication Date
JPS61191547A JPS61191547A (en) 1986-08-26
JPH0645492B2 true JPH0645492B2 (en) 1994-06-15

Family

ID=12270596

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2923685A Expired - Lifetime JPH0645492B2 (en) 1985-02-19 1985-02-19 Admixture for concrete and mortar

Country Status (1)

Country Link
JP (1) JPH0645492B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010008092A1 (en) * 2008-07-18 2010-01-21 花王株式会社 Method for producing hydraulic powder
US8598255B2 (en) * 2008-07-18 2013-12-03 Kao Corporation Early strengthening agent for hydraulic composition

Also Published As

Publication number Publication date
JPS61191547A (en) 1986-08-26

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