JPH01172250A - Retardant for cement - Google Patents
Retardant for cementInfo
- Publication number
- JPH01172250A JPH01172250A JP32963787A JP32963787A JPH01172250A JP H01172250 A JPH01172250 A JP H01172250A JP 32963787 A JP32963787 A JP 32963787A JP 32963787 A JP32963787 A JP 32963787A JP H01172250 A JPH01172250 A JP H01172250A
- Authority
- JP
- Japan
- Prior art keywords
- cement
- polymer
- ethylene
- vinyl acetate
- retardant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000004568 cement Substances 0.000 title claims abstract description 32
- 229920000642 polymer Polymers 0.000 claims abstract description 23
- 239000000839 emulsion Substances 0.000 claims abstract description 18
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000005977 Ethylene Substances 0.000 claims abstract description 11
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 238000007334 copolymerization reaction Methods 0.000 claims description 4
- 230000000694 effects Effects 0.000 abstract description 9
- HFCUBKYHMMPGBY-UHFFFAOYSA-N 2-methoxyethyl prop-2-enoate Chemical compound COCCOC(=O)C=C HFCUBKYHMMPGBY-UHFFFAOYSA-N 0.000 abstract description 6
- 230000000979 retarding effect Effects 0.000 abstract description 5
- 239000007787 solid Substances 0.000 abstract description 5
- FWWXYLGCHHIKNY-UHFFFAOYSA-N 2-ethoxyethyl prop-2-enoate Chemical compound CCOCCOC(=O)C=C FWWXYLGCHHIKNY-UHFFFAOYSA-N 0.000 abstract description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 abstract 2
- 230000000379 polymerizing effect Effects 0.000 abstract 2
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 1
- 239000000178 monomer Substances 0.000 description 16
- 239000004570 mortar (masonry) Substances 0.000 description 10
- 230000000704 physical effect Effects 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000005038 ethylene vinyl acetate Substances 0.000 description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- -1 oxycarboxylate Polymers 0.000 description 4
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- XWNVSPGTJSGNPU-UHFFFAOYSA-N ethyl 4-chloro-1h-indole-2-carboxylate Chemical compound C1=CC=C2NC(C(=O)OCC)=CC2=C1Cl XWNVSPGTJSGNPU-UHFFFAOYSA-N 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- PTJDGKYFJYEAOK-UHFFFAOYSA-N 2-butoxyethyl prop-2-enoate Chemical group CCCCOCCOC(=O)C=C PTJDGKYFJYEAOK-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 241001553014 Myrsine salicina Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 229920006328 Styrofoam Polymers 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- XBNZGFLFMOQEFF-UHFFFAOYSA-M azanium sodium hydrogen sulfate acetate Chemical compound C(C)(=O)[O-].[Na+].S(=O)(=O)([O-])O.[NH4+] XBNZGFLFMOQEFF-UHFFFAOYSA-M 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229910052810 boron oxide Inorganic materials 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000011083 cement mortar Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004815 dispersion polymer Substances 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical class CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000011414 polymer cement Substances 0.000 description 1
- 239000011433 polymer cement mortar Substances 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008261 styrofoam Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/2688—Copolymers containing at least three different monomers
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は高分子からなるセメント用混和剤、詳しくはセ
メント用遅延剤に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a cement admixture made of a polymer, and more particularly to a cement retarder.
〈従来の技術とその問題点〉
一般にセメント用遅延剤はセメントの水和反応を遅らせ
ることにより、モルタルやコンクリートの凝結、硬化を
遅延させるセメント用混和剤である。<Prior art and its problems> In general, cement retarders are admixtures for cement that delay the setting and hardening of mortar and concrete by delaying the hydration reaction of cement.
従来セメント用遅延剤としては、無機系及び有機系の2
種類があり、例えば無機系では、酸化鉛、酸化ホウ素、
ホウ砂、塩化亜鉛、酸化亜鉛及び珪フン化マグネシウム
等が、又、有機系では、砂糖、アルコール、メチルセル
ロース・エチルセルロース・ポリビニルアルコール・デ
キストリン及びポリアクリル酸ソーダ等のポリハイドロ
キシ化合物、オキシカルボン酸塩、リグニンスルホン酸
塩及びグルコン酸塩等が使用されている。そしてその使
用目的は、夏期における生コンの長時間輸送への対処、
連続打設におけるコールドジヨイントの防止、夜間作業
の廃止、打継目の一体化、大型化したコンクリート構造
物における温度応力の緩和などである。Conventional retarders for cement include two types: inorganic and organic.
There are various types; for example, inorganic types include lead oxide, boron oxide,
Borax, zinc chloride, zinc oxide, magnesium silicate, etc., and in organic systems, sugar, alcohol, polyhydroxy compounds such as methyl cellulose, ethyl cellulose, polyvinyl alcohol, dextrin, and sodium polyacrylate, oxycarboxylate, Lignosulfonate, gluconate, etc. are used. The purpose of its use is to cope with the long transportation of ready-mixed concrete in the summer,
These include preventing cold joints in continuous pouring, eliminating nighttime work, integrating pouring joints, and alleviating temperature stress in larger concrete structures.
一方セメント水和物に起因する引張り強度、乾燥収縮性
及び耐薬品性などの欠点を改善する目的で、モルタルや
コンクリートヘエチレンー酢酸ビニル共重合体エマルジ
ョン(EVA)やアクリル酸エステル共重合体エマルジ
ジンのような樹脂エマルジョンあるいはスチレンブタジ
ェンゴム(S B R)のようなゴムラテックスを混和
することが行なわれており、最近ではこれらを併用した
ポリマーセメントも汎用の建設材料として大量に消費さ
れている。On the other hand, in order to improve the shortcomings such as tensile strength, drying shrinkage and chemical resistance caused by cement hydrate, ethylene-vinyl acetate copolymer emulsion (EVA) and acrylic ester copolymer emulsion are used for mortar and concrete. It is common practice to mix resin emulsions such as these or rubber latexes such as styrene-butadiene rubber (SBR), and recently polymer cements using these in combination have also been consumed in large quantities as general-purpose construction materials. .
〈問題点を解決するための手段〉
本発明者は、セメント用遅延剤及びポリマーの併用頻度
が増えていることに着目し、セメント用ポリマーに本来
のモルタルやコンクリートの物性改善作用を損なわずに
遅延剤としての作用を付与しセメント用遅延剤に係る上
記の問題点を解決すべく鋭意検討を重ねた結果、特定の
モノマーを使用することにより前述の問題を解決するこ
とを見出し本発明を完成した。<Means for Solving the Problems> The present inventor has focused on the increasing frequency of using cement retardants and polymers in combination, and has developed a method for adding cement polymers to cement polymers without impairing their inherent ability to improve the physical properties of mortar and concrete. As a result of intensive studies to solve the above-mentioned problems related to retarders for cement by imparting them with a function as a retarder, we discovered that the above-mentioned problems could be solved by using a specific monomer, and completed the present invention. did.
即ち、本発明は一般式CI2 = CHC00CHzC
fl□0R(Rは炭素数1〜5のアルキル基を表わす)
で示される化合物、エチレン及び酢酸ビニルを乳化共重
合したポリマーを主成分とするセメント用遅延剤である
。That is, the present invention has the general formula CI2=CHC00CHzC
fl□0R (R represents an alkyl group having 1 to 5 carbon atoms)
This is a retarder for cement whose main component is a polymer obtained by emulsion copolymerization of the compound represented by the above formula, ethylene, and vinyl acetate.
以下本発明の詳細な説明する。The present invention will be explained in detail below.
一般式CI2 = CHC00CHzCIIzOR(以
下一般式Aという)は通常アクリル酸エステルと呼ばれ
るものに属し、Rは炭素数1〜5のアルキル基で、なか
でも炭素数1〜2のアルキル基が好ましい。The general formula CI2=CHC00CHzCIIzOR (hereinafter referred to as general formula A) belongs to what is usually called an acrylic ester, and R is an alkyl group having 1 to 5 carbon atoms, and an alkyl group having 1 to 2 carbon atoms is particularly preferable.
一般式Aで示されるモノマー(以下本モノマーという)
としては、2−メトキシエチルアクリレート、2−エト
キシエチルアクリレート及び2−ブトキシエチルアクリ
レートなどがある。Monomer represented by general formula A (hereinafter referred to as the present monomer)
Examples include 2-methoxyethyl acrylate, 2-ethoxyethyl acrylate and 2-butoxyethyl acrylate.
本モノマーと共重合できるものとしてはエチレンや酢酸
ビニルをはじめとする( CHz=CII )構造を
有するモノマーであればほとんど使用可能であるが、セ
メント物性改良の面からエチレン−酢酸ビニルと共重合
することが好ましい。Most monomers that can be copolymerized with this monomer have a (CHz=CII) structure, including ethylene and vinyl acetate, but from the perspective of improving the physical properties of cement, copolymerization with ethylene-vinyl acetate can be used. It is preferable.
以下本モノマーとエチレン−酢酸ビニルの共IJ合に関
して説明する。The co-IJ combination of the present monomer and ethylene-vinyl acetate will be explained below.
エチレン−酢酸ビニルと本モノマーとからなる三元共重
合体エマルジョン(以下本エマルジョンという)中のエ
チレン含量は、5〜40重量%が好ましい。エチレン含
量が5重量%未満では、セメントに混入した場合、本エ
マルジョン中の酢酸ビニルがアルカリで加水分解を受け
やすくなるので好ましくない。一方、40重量%を越す
と安定なエマルジョンが得られない。The ethylene content in the terpolymer emulsion (hereinafter referred to as the present emulsion) consisting of ethylene-vinyl acetate and the present monomer is preferably 5 to 40% by weight. If the ethylene content is less than 5% by weight, the vinyl acetate in the emulsion will be easily hydrolyzed by alkali when mixed into cement, which is not preferable. On the other hand, if it exceeds 40% by weight, a stable emulsion cannot be obtained.
更に、本エマルジョン中の本モノマー含量は1〜40重
量%が好ましい。1重量%未満では、セメントに対する
遅延作用が十分でなく、一方、40重量%を越すとセメ
ントとの混和性が悪くなる恐れがある。Furthermore, the content of the present monomer in the present emulsion is preferably 1 to 40% by weight. If it is less than 1% by weight, the retarding effect on cement will not be sufficient, while if it exceeds 40% by weight, the miscibility with cement may deteriorate.
本発明の本エマルジョンの製造方法については特に制限
はなく、乳化重合方法は公知の方法を使用することが出
来る。但し、前述の本モノマーは反応性が高いため、重
合中連続的に添加し、均一に共重合せしめた方がよい。There are no particular limitations on the method for producing the emulsion of the present invention, and any known emulsion polymerization method can be used. However, since the aforementioned monomer has high reactivity, it is better to add it continuously during the polymerization to achieve uniform copolymerization.
本モノマー全量を重合缶に仕込んで反応を開始すると、
本モノマーのホモポリマーが生成しやすくなり、セメン
トとの混和性が悪くなる場合がある。When the entire amount of this monomer is charged into a polymerization reactor and the reaction is started,
A homopolymer of this monomer is likely to be formed, which may result in poor miscibility with cement.
重合条件には特に制限はないが、−船釣には重合温度2
0〜80℃、重合圧力10〜90kg/cn!が利用さ
れる。乳化剤は、例えばポリビニルアルコール、メチル
セルロース及びヒドロキシエチルセルロース等の保護コ
ロイド、ポリオキシエチレン縮合体、ポリオキシエチレ
ンポリオキシプロピレンブロックコポリマー等の非イオ
ン性界面活性剤、アルキルベンゼンスルホン酸塩及びラ
ウリル硫酸エステル塩等のアニオン性界面活性剤が挙げ
られる。これらは単独又は2種以上を組合せて用いるこ
とができる。There are no particular restrictions on the polymerization conditions, but - for boat fishing, the polymerization temperature is 2.
0~80℃, polymerization pressure 10~90kg/cn! is used. Examples of emulsifiers include polyvinyl alcohol, protective colloids such as methyl cellulose and hydroxyethyl cellulose, nonionic surfactants such as polyoxyethylene condensates and polyoxyethylene polyoxypropylene block copolymers, and alkylbenzene sulfonates and lauryl sulfate salts. Examples include anionic surfactants. These can be used alone or in combination of two or more.
触媒としては、過硫酸カリウム等の過硫酸塩、過酸化水
素及び各種有機過酸化物等が挙げられる。Examples of the catalyst include persulfates such as potassium persulfate, hydrogen peroxide, and various organic peroxides.
レドックス開始系の場合は、さらに還元性物質としてホ
ルムアルデヒドナトリウムスルホキシレートなどが組み
合せて用いられる。In the case of a redox initiation system, a reducing substance such as formaldehyde sodium sulfoxylate is further used in combination.
さらに必要に応じ、公知のpH1jJ整剤(バッファー
)、消泡剤及び防腐剤等の添加剤の使用が可能である。Furthermore, if necessary, known additives such as a pH 1jJ adjuster (buffer), an antifoaming agent, and a preservative can be used.
本エマルジョン中の固形分は、共重合するモノマー量と
水により調整されるが、40〜65重量%が工業的見地
から好ましい。The solid content in this emulsion is adjusted by the amount of monomers to be copolymerized and water, but is preferably 40 to 65% by weight from an industrial standpoint.
以上の方法で得られた本エマルジョンのモルタルやコン
クリートへの添加量は、セメント100重量部に対して
固形分で2〜20重量部が好ましく2重量部未満では、
モルタルやコンクリートへの物性改善効果及び水和反応
遅延効果が十分でなく、一方20重量%を越すとセメン
トとの混和性が悪くなる恐れがある。The amount of the present emulsion obtained by the above method added to mortar or concrete is preferably 2 to 20 parts by weight in terms of solid content per 100 parts by weight of cement, and less than 2 parts by weight.
The effect of improving the physical properties of mortar and concrete and the effect of retarding the hydration reaction are insufficient, and on the other hand, if the amount exceeds 20% by weight, the miscibility with cement may deteriorate.
なお、本発明で得られるエマルジョンは、SBR、ポリ
アクリレート等の公知のセメント用ポリマー、AE剤、
減水剤、流動化剤、収縮調整剤、防錆剤、防水剤及び防
凍剤等のセメント用混和剤との併用が可能である。The emulsion obtained in the present invention may contain known cement polymers such as SBR and polyacrylate, AE agents,
It can be used in combination with cement admixtures such as water reducers, fluidizers, shrinkage regulators, rust preventives, waterproofing agents, and antifreeze agents.
〈実施例〉 以下実施例で本発明をさらに説明する。<Example> The present invention will be further explained below with reference to Examples.
実施例1
内容積101のステンレス製電磁攪拌機付オートクレー
ブに次の原料を仕込んだ。Example 1 The following raw materials were charged into a stainless steel autoclave equipped with an electromagnetic stirrer and having an internal volume of 101 cm.
純水 2.650 g
酢酸ビニル 2.280 gキシプロピレ
ン
ブロック共重合
体)
ハイドロキシエチル 45g(フジ化学工業セルロー
ス 社製)
「ハイテノールN−17J 22.5g (第一工業
製薬社製ポリオキシ
アルキル(又は
アリル)サルフ
エートのアンモ
ニウム塩
酢酸ソーダ 12g
内温を70℃まで上げてエチレンを50kg/calと
なるまで導入した。触媒として過硫酸アンモニウム0.
6gを添加し重合を開始した。内湯はジャケットの温度
を調整して一定に保った。Pure water 2.650 g Vinyl acetate 2.280 g xypropylene block copolymer) Hydroxyethyl 45 g (manufactured by Fuji Chemical Cellulose Co., Ltd.) Hitenol N-17J 22.5 g (polyoxyalkyl (manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) or allyl) sulfate ammonium salt Sodium acetate 12g The internal temperature was raised to 70°C and ethylene was introduced to 50kg/cal. Ammonium persulfate was added as a catalyst.
6 g was added to start polymerization. The temperature of the indoor bath was kept constant by adjusting the jacket.
又、本モノマーとして2−メトキシエチルアクリレート
(東亜合成化学工業型、商品名[アクリレートC−IJ
570gを重合開始時より8時間にわたって均一に連続
的に分添した。In addition, as this monomer, 2-methoxyethyl acrylate (Toagosei Chemical Industry type, trade name [Acrylate C-IJ
570 g was uniformly and continuously added in portions over 8 hours from the start of polymerization.
10時間の後、冷却した内容物を取り出した。After 10 hours, the cooled contents were removed.
内容物は粗粒の少ない安定なエマルジョンで固形分52
.5重量%、粘度3.700cpsで、そのポリマー組
成は酢酸ビニルユニット66重量%、エチレンユニット
17重量%、2−メトキシエチルアクリレートユニット
17重量%であった。(ポリマーAという。)
モノマーとして2−メトキシエチルアクリレートのかわ
りに、2−ブトキシエチルアクリレート(大阪有機化学
社製)、炭素数4を用いた他は、ポリマーAと全(同様
の方法で製造した。The content is a stable emulsion with few coarse particles, solid content 52
.. 5% by weight, viscosity 3.700 cps, and its polymer composition was 66% by weight vinyl acetate units, 17% by weight ethylene units, and 17% by weight 2-methoxyethyl acrylate units. (referred to as Polymer A) Polymer A and Polymer A (produced in the same manner) except that 2-butoxyethyl acrylate (manufactured by Osaka Organic Chemical Co., Ltd.) with 4 carbon atoms was used instead of 2-methoxyethyl acrylate as a monomer. .
得られたエマルジョンは安定であり、固形分52.1重
量%、粘度3.900cpsで、そのポリマー組成は酢
酸ビニルユニ、トロ5重量%、エチレンユニット16重
量%、2−ブトキシエチルアクリレートユニット19重
量%であった。(ポリマーBという。)
下記に示す材料を用い、表に示す割合の配合物を調製し
た。調製法はJisAl 171 r試験室におけるポ
リマーセメントモルタルの作り方」に準じた。The resulting emulsion was stable, with a solid content of 52.1% by weight and a viscosity of 3.900 cps, and its polymer composition was vinyl acetate uni, 5% by weight of Toro, 16% by weight of ethylene units, and 19% by weight of 2-butoxyethyl acrylate units. Met. (referred to as Polymer B) Using the materials shown below, formulations were prepared in the proportions shown in the table. The preparation method was in accordance with "How to make polymer cement mortar in JisAl 171r test laboratory".
(1) セメント 普通ポルトランドセメント(2
)骨 材 豊浦標準砂
(3) ポリマーA 本モノマーとして2−メトキシ
エチルアクリレート使用
ポリマーB 本モノマーとして2−ブトキシエチルアク
リレート使用
〃 C電気化学工業側型「デンカ
EVAテックス#83」
(固形分55%、粘度4 、800
cps 、組成:エチレン/酢酸
ビニル= 20/80 ”)
なお、物性測定は次の方法によった。(1) Cement Ordinary Portland cement (2
) Aggregate Toyoura standard sand (3) Polymer A: 2-methoxyethyl acrylate is used as the main monomer. Polymer B: 2-butoxyethyl acrylate is used as the main monomer. , viscosity 4, 800 cps, composition: ethylene/vinyl acetate = 20/80'') The physical properties were measured by the following method.
(1) モルタル物性 ポリマー添加量を変えた以
外はJisA6203
「セメント混和用ポリマ
ーディスバージョン」に
準拠した。(1) Mortar physical properties Compliant with JIS A6203 "Polymer dispersion for cement mixing" except that the amount of polymer added was changed.
(2)遅延剤の効果 周囲を発泡スチロールで包んで
断熱状態にした塩
ビ製の容器に(ポリマー)
セメントモルタルを1 kg
入れ、容器に感温体を挿
入して水和反応に伴なう
発熱の状態を室温との温
度差(ΔT)として経時
的に記録した。(2) Effect of retardant 1 kg of (polymer) cement mortar was placed in a PVC container wrapped with styrofoam to provide insulation, and a thermosensor was inserted into the container to suppress the heat generated by the hydration reaction. Conditions were recorded over time as a temperature difference (ΔT) from room temperature.
(3)混線状態
モルタルをモルタル練り混ぜ用のはちで練り混ぜた時、
かなりの力を入れないと混練困難な場合を「不良」とし
、その他を「良」とした。(3) When mixed mortar is mixed with a mortar mixer,
Cases in which kneading was difficult without applying considerable force were rated as "poor," and other cases were rated as "good."
に比べてモルタル物性の改善作用とセメントとの硬化遅
延作用が認められ、しかもポリマー添加量により硬化遅
延の程度が異なることが判る。It was found that the effect of improving the physical properties of the mortar and the effect of retarding the hardening with cement were observed, and it was also found that the degree of hardening retardation differed depending on the amount of polymer added.
〈発明の効果〉
本発明により、モルタルやコンクリートの物性改善作用
と硬化遅延作用を併せ持つセメント混和用ポリマーを得
ることができる。<Effects of the Invention> According to the present invention, it is possible to obtain a polymer for mixing in cement that has both the effect of improving the physical properties of mortar and concrete and the effect of retarding hardening.
特許出願人 電気化学工業株式会社
手続補正書(自発)
昭和63年2月19日
特許庁長官 小 川 邦 夫 殿
1、事件の表示
昭和62年特許願第329637号
2、発明の名称
セメント用遅延剤
6、補正をする者
事件との関係 特許出願人
住所 ■100 東京都千代田区有楽町1丁目4番1
号明細書の発明の詳細な説明の欄
5、補正の内容
5−1. 明細書第12貞表を別紙のとお9訂正する
。Patent applicant Denki Kagaku Kogyo Co., Ltd. Procedural amendment (voluntary) February 19, 1985 Director General of the Patent Office Kunio Ogawa 1, Indication of the case 1988 Patent Application No. 329637 2, Name of the invention Delay for cement Agent 6. Relationship with the person making the amendment Patent applicant address ■100 1-4-1 Yurakucho, Chiyoda-ku, Tokyo
Column 5 of detailed explanation of the invention in the specification of No. 5, contents of amendment 5-1. The 12th statement of the specification is amended as shown in the attached sheet.
Claims (1)
(Rは炭素数1〜5のアルキル基を表わす)で示される
化合物、エチレン及び酢酸ビニルを乳化共重合したポリ
マーを主成分とするセメント用遅延剤。General formula CH_2=CH=-COOCH_2CH_2OR
(R represents an alkyl group having 1 to 5 carbon atoms), a cement retarder whose main component is a polymer obtained by emulsion copolymerization of ethylene and vinyl acetate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32963787A JPH01172250A (en) | 1987-12-28 | 1987-12-28 | Retardant for cement |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32963787A JPH01172250A (en) | 1987-12-28 | 1987-12-28 | Retardant for cement |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01172250A true JPH01172250A (en) | 1989-07-07 |
Family
ID=18223566
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP32963787A Pending JPH01172250A (en) | 1987-12-28 | 1987-12-28 | Retardant for cement |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01172250A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0823409A1 (en) * | 1996-08-06 | 1998-02-11 | Daicel-Huels Ltd. | Cement retarder and cement retardative sheet |
US5782972A (en) * | 1997-03-21 | 1998-07-21 | W.R. Grace & Co.-Conn. | Additive for production of highly workable mortar cement |
US5932344A (en) * | 1995-02-07 | 1999-08-03 | Daicel-Huels Ltd. | Cement retarder and cement retardative sheet |
US6451880B1 (en) | 1998-11-23 | 2002-09-17 | W. R. Grace & Co.-Conn. | Workability and board life in masonry mortar and method for obtaining same |
EP1631646A1 (en) * | 2003-05-27 | 2006-03-08 | Basf Aktiengesellschaft | Fuel compound exhibiting improved cold flow properties |
-
1987
- 1987-12-28 JP JP32963787A patent/JPH01172250A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5932344A (en) * | 1995-02-07 | 1999-08-03 | Daicel-Huels Ltd. | Cement retarder and cement retardative sheet |
US6114033A (en) * | 1995-02-07 | 2000-09-05 | Daicel-Huels Ltd. | Cement retarder and cement retardative sheet |
EP0823409A1 (en) * | 1996-08-06 | 1998-02-11 | Daicel-Huels Ltd. | Cement retarder and cement retardative sheet |
US6077910A (en) * | 1996-08-06 | 2000-06-20 | Daicel-Huels Ltd. | Cement retarder and cement retardative sheet |
US6376580B1 (en) | 1996-08-06 | 2002-04-23 | Daicel-Huels Ltd. | Cement retarder and cement retardative sheet |
US5782972A (en) * | 1997-03-21 | 1998-07-21 | W.R. Grace & Co.-Conn. | Additive for production of highly workable mortar cement |
US6451880B1 (en) | 1998-11-23 | 2002-09-17 | W. R. Grace & Co.-Conn. | Workability and board life in masonry mortar and method for obtaining same |
EP1631646A1 (en) * | 2003-05-27 | 2006-03-08 | Basf Aktiengesellschaft | Fuel compound exhibiting improved cold flow properties |
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