JP2000219558A - Lightweight aerated concrete excellent in carbonation resistance - Google Patents

Lightweight aerated concrete excellent in carbonation resistance

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Publication number
JP2000219558A
JP2000219558A JP2437199A JP2437199A JP2000219558A JP 2000219558 A JP2000219558 A JP 2000219558A JP 2437199 A JP2437199 A JP 2437199A JP 2437199 A JP2437199 A JP 2437199A JP 2000219558 A JP2000219558 A JP 2000219558A
Authority
JP
Japan
Prior art keywords
alc
carbonation
resistance
weight
water
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
Application number
JP2437199A
Other languages
Japanese (ja)
Inventor
Fumiaki Matsushita
文明 松下
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.)
Sumitomo Metal Mining Co Ltd
Original Assignee
Sumitomo Metal Mining 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 Sumitomo Metal Mining Co Ltd filed Critical Sumitomo Metal Mining Co Ltd
Priority to JP2437199A priority Critical patent/JP2000219558A/en
Priority to AU60066/99A priority patent/AU6006699A/en
Priority to EP99973406A priority patent/EP1055648A4/en
Priority to PCT/JP1999/005585 priority patent/WO2000035827A1/en
Publication of JP2000219558A publication Critical patent/JP2000219558A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To suppress water repellency and to give excellent carbonation resistance and enough water absorbing property by incorporating a small amt. of a dimethylpolysiloxane having side chains all being methyl groups to a lightweight aerated concrete having a siliceous component and a lime component as the main components. SOLUTION: A siliceous source material such as quartzite and a lime source material such as a cement and quicklime are used in a fine powder state as the main materials, to which water and an additive such as aluminum powder are added to prepare a slurry. The slurry is aerated by the reaction of the aluminum powder, semi-hardened by the reaction of the lime source material, and then formed into a specified dimension. Then the product is subjected to high temp. high pressure steam cure in an autoclave to obtain a lightweight aerated concrete(ALC). Dimethylpolysiloxane having side chains all being methyl groups is added by 0.001 to 0.18 wt.% to the ALC to obtain the cobjectiver ALC having excellent carbonation resistance. Since the obtd. ALC has excellent carbonation resistance, it also has excellent ageing resistance and durability. Further, with enough water absorbing property, it does not cause frost damage.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、建築物の壁、屋
根、床などに使用される耐炭酸化性に優れた軽量気泡コ
ンクリートに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to lightweight cellular concrete excellent in carbonation resistance used for walls, roofs, floors and the like of buildings.

【0002】[0002]

【従来の技術】軽量気泡コンクリート(以下、ALCと
記す)は、軽量で、耐火性・断熱性・施工性に優れてい
るため、建築材料として広く使用されている。
2. Description of the Related Art Light-weight cellular concrete (hereinafter referred to as ALC) is widely used as a building material because it is lightweight and has excellent fire resistance, heat insulation and workability.

【0003】ALCは次のようにして製造される。すな
わち、珪石などの珪酸質原料と、セメント・生石灰など
の石灰質原料とを主原料とし、これらの微粉末に水とア
ルミニウム粉末などの添加物とを加えてスラリー状とす
る。このスラリーを、アルミニウム粉末の反応により発
泡させ、石灰質原料の反応により半硬化させて、所定寸
法に成形する。その後、オートクレーブによる高温高圧
水蒸気養生を行ってALCとする。
[0003] ALC is manufactured as follows. That is, a siliceous raw material such as silica stone and a calcareous raw material such as cement and quicklime are used as main raw materials, and water and an additive such as aluminum powder are added to these fine powders to form a slurry. The slurry is foamed by the reaction of the aluminum powder, semi-cured by the reaction of the calcareous raw material, and formed into a predetermined size. Thereafter, high-temperature and high-pressure steam curing is performed by an autoclave to obtain ALC.

【0004】このようにして製造されたALCは、珪酸
質成分および石灰質成分を主成分とし、主要構成鉱物が
トバモライトである。そして、気泡と細孔が全体積の約
8割を占める空隙の非常に多い微細構造を持ち、絶乾か
さ比重が約0.5程度である。
[0004] The ALC thus produced contains a siliceous component and a calcareous component as main components, and the main constituent mineral is tobermorite. It has a microstructure with very large voids, in which bubbles and pores occupy about 80% of the total volume, and has a specific gravity of about 0.5 in absolute dryness.

【0005】上記のようにALCは気泡と細孔が非常に
多いので、水分やガス(炭酸ガスなど)は容易にALC
内部へ浸入する。ALCの主要構成鉱物であるトバモラ
イトは、浸入した水分と炭酸ガスと反応し、シリカゲル
と炭酸カルシウムとに分解する。これが炭酸化である。
炭酸化は、炭酸化現象、すなわち強度の低下、ひび割れ
の発生などの劣化をALCに引き起こす。そこで、AL
Cの炭酸化を防止するか遅延させるために、(1)水分
や炭酸ガスの浸入を防ぐこと、(2)トバモライトに耐
炭酸化性を持たせることが求められる。根本的な対策と
なり得るので期待される上記(2)に対する手段は、種
々の研究にもかかわらず、工業的に有効なものが見出さ
れていない。そのため、上記(1)に対する手段、すな
わちALCの表面仕上げ(塗装など)がこれまで専ら用
いられていた。
[0005] As described above, ALC has a large number of bubbles and pores, so that moisture and gas (such as carbon dioxide) can be easily removed by ALC.
Infiltrate inside. Tobermorite, the main constituent mineral of ALC, reacts with the infiltrated water and carbon dioxide to decompose into silica gel and calcium carbonate. This is carbonation.
Carbonation causes ALC to undergo a carbonation phenomenon, that is, deterioration such as a decrease in strength and generation of cracks. So AL
In order to prevent or delay carbonation of C, it is required to (1) prevent the intrusion of moisture and carbon dioxide gas, and (2) to make tobermorite resistant to carbonation. As a means for the above (2), which can be a fundamental measure, no industrially effective means has been found despite various studies. Therefore, the means for the above (1), that is, the ALC surface finish (painting or the like) has been exclusively used until now.

【0006】しかしながら、ALCの表面仕上げによる
耐炭酸化性の向上は十分でなく、また使用年数と共に炭
酸化が進行することが確認されている。
[0006] However, it has been confirmed that the improvement of the carbonation resistance by the surface finish of ALC is not sufficient, and that the carbonation progresses with the years of use.

【0007】なお、炭酸化の原因となる水分の浸入を防
ぐことに関して、オルガノポリシロキサンを添加すると
ALCに撥水性が付与されることが知られている。例え
ば、特開昭55−42272号公報にはジメチルポリシ
ロキサンを0.2〜10重量%添加すること、特公平1
−58148公報にはアルキル基を含むオルガノポリシ
ロキサンを0.05〜10重量%添加することが記載さ
れている。
[0007] Regarding the prevention of intrusion of moisture which causes carbonation, it is known that the addition of organopolysiloxane imparts water repellency to ALC. For example, JP-A-55-42272 discloses that dimethylpolysiloxane is added in an amount of 0.2 to 10% by weight.
JP-A-58148 describes that 0.05 to 10% by weight of an organopolysiloxane containing an alkyl group is added.

【0008】しかしながら、これらの撥水性ALCは、
耐炭酸化性が優れるものも、優れないものも含む。ま
た、一般に耐候性に優れるといわれているが、凍害現象
がしばしば起きる。凍害現象は、撥水性に優れるが故に
屋外側もしくは屋内側の塗装仕上げ層とALCとの間に
水分が溜まりやすく、冬季にここに溜まった水分が凍結
して塗装が剥がれたり膨れてしまう現象である。この凍
害現象は、撥水性や耐炭酸化性に劣る(その分、吸水性
がある)一般的なALCでは見られない。
However, these water repellent ALCs are
Some include those having excellent resistance to carbonation, and others not. In addition, although it is generally said that the weather resistance is excellent, a frost damage phenomenon often occurs. The frost damage phenomenon is a phenomenon in which water is easily accumulated between the ALC and the paint finish layer on the outdoor side or the indoor side due to its excellent water repellency, and the water that has accumulated here freezes in winter and the paint peels off or swells. is there. This frost damage phenomenon is not seen in general ALC which is inferior in water repellency and carbonation resistance (has a corresponding amount of water absorption).

【0009】従って、撥水性ALCは、単体を見た場合
は耐候性に優れるが、建築物全体から見た場合には問題
である。これが、撥水性ALCが使用範囲に制限を受
け、建築物全般に広く用いられていない(生産量は全生
産量の1〜2%と非常に少ない)原因であると考えられ
る。
Therefore, the water-repellent ALC is excellent in weather resistance when viewed alone, but is problematic when viewed from the whole building. This is considered to be the reason that the water-repellent ALC is limited in its use range and is not widely used in buildings in general (the production amount is as very small as 1 to 2% of the total production amount).

【0010】[0010]

【発明が解決しようとする課題】本発明の目的は、上記
事情に鑑み、撥水性が抑止され、耐炭酸化性に優れ、か
つ吸水性が十分であるALCを提供することにある。
SUMMARY OF THE INVENTION In view of the above circumstances, an object of the present invention is to provide an ALC having reduced water repellency, excellent carbonation resistance, and sufficient water absorption.

【0011】[0011]

【課題を解決するための手段】本発明者は、上記目的を
達成すべく、様々な研究と試行錯誤を行った結果、「種
々のオルガノポリシロキサンを少量添加したALCは、
撥水性が低下して吸水性が向上すると同時に、耐炭酸化
性に依然として優れる」ことを発見し本発明に到達し
た。
Means for Solving the Problems The present inventor has conducted various studies and trial and error in order to achieve the above object, and as a result, it has been found that "ALC containing a small amount of various organopolysiloxanes is
The water repellency is reduced and the water absorption is improved, and at the same time, the carbonation resistance is still excellent. "

【0012】すなわち、本発明の耐炭酸化性に優れるA
LCは、珪酸質成分および石灰質成分を主成分とするA
LCにおいて、側鎖がすべてメチル基であるジメチルポ
リシロキサンを0.001〜0.18重量%含むことを
特徴とする。
That is, according to the present invention, A is excellent in carbonation resistance.
LC is A having a siliceous component and a calcareous component as main components.
The LC is characterized by containing 0.001 to 0.18% by weight of dimethylpolysiloxane whose side chains are all methyl groups.

【0013】[0013]

【発明の実施の形態】特開昭55−42272号公報に
は、前述したように、ジメチルポリシロキサンを0.2
〜10重量%添加した撥水性ALCが記載されている。
このALCの撥水性発現機構は、ジメチルポリシロキサ
ンの添加により多孔質であるALCと水との接触角を変
化させ、毛細管現象による該ALCへの水の浸入を防ぐ
というものであり、該接触角を十分変化させるために上
記程度の添加量が必要であったと考えられる。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Japanese Patent Application Laid-Open No. 55-42272 discloses that, as described above,
A water repellent ALC with an addition of 〜1010% by weight is described.
The mechanism of exhibiting the water repellency of ALC is to change the contact angle between porous ALC and water by adding dimethylpolysiloxane, thereby preventing water from entering the ALC due to capillary action. It is considered that the above-mentioned amount of addition was necessary to sufficiently change the amount.

【0014】一方、本発明の耐炭酸化性に優れるALC
は、側鎖がすべてメチル基であるジメチルポリシロキサ
ンを0.001〜0.18重量%含む。このようにジメ
チルポリシロキサン添加量が少なくても耐炭酸化性が優
れるのは、「耐炭酸化性において重要なのは、液体の水
ではなく、気体である水蒸気や6分子層程度の表面吸着
水である。これらの水蒸気や吸着水がトバモライト表面
に存在する状態を変えるためには、上記のような少ない
添加量で十分である。」と考えられるからである。添加
量が0.001重量%未満では、耐炭酸化性が十分でな
く、一方0.18重量%を超えると、吸水性が低下す
る。
On the other hand, the ALC of the present invention having excellent resistance to carbonation
Contains 0.001 to 0.18% by weight of dimethylpolysiloxane in which all side chains are methyl groups. The fact that the carbonation resistance is excellent even with a small amount of dimethylpolysiloxane added is that the important thing in carbonation resistance is not water but liquid gas such as water vapor or surface-adsorbed water of about 6 molecular layers. In order to change the state in which the water vapor and the adsorbed water are present on the surface of tobermorite, the above-mentioned small amount is sufficient. " If the amount added is less than 0.001% by weight, the resistance to carbonation is not sufficient, while if it exceeds 0.18% by weight, the water absorption decreases.

【0015】[0015]

【実施例】以下、実施例により本発明をより詳細に説明
する。
The present invention will be described in more detail with reference to the following examples.

【0016】[実施例1〜7、比較例1〜3、従来例
1]珪酸質原料、石灰質原料および繰り返し原料を混合
し、40重量%の珪酸質原料、40重量%の石灰質原料
および20重量%の繰り返し原料からなる主原料混合物
を得た。この際、珪酸質原料には珪石を用い、石灰質原
料には生石灰、セメントおよび石膏を用いた。また、4
0重量%の石灰質原料の内訳は、生石灰が5重量%、セ
メントが30重量%および石膏が5重量%である。
[Examples 1 to 7, Comparative Examples 1 to 3, Conventional Example 1] A siliceous raw material, a calcareous raw material and a repeated raw material were mixed, and the mixture was mixed with 40% by weight of a siliceous raw material, 40% by weight of a calcareous raw material, and 20% by weight. % Of a repeating raw material was obtained. At this time, silica stone was used as the siliceous raw material, and quicklime, cement and gypsum were used as the calcareous raw material. Also, 4
The breakdown of the 0% by weight calcareous raw material is 5% by weight of quicklime, 30% by weight of cement and 5% by weight of gypsum.

【0017】この主原料混合物に水、アルミニウム粉末
および界面活性剤を加えて混練し、スラリーを作成し
た。この際、側鎖がすべてメチル基であるジメチルポリ
シロキサンを添加しないスラリー(従来例1)および添
加したスラリー(実施例1〜7、比較例1〜3)を作成
した。スラリーへの添加量は、0.0005重量%(比
較例1)、0.001重量%(実施例1)、0.005
重量%(実施例2)、0.01重量%(実施例3)、
0.05重量%(実施例4)、0.10重量%(実施例
5)、0.15重量%(実施例6)、0.18重量%
(実施例7)、0.20重量%(比較例2)および0.
30重量%(比較例3)とした。また、水・固体比(重
量)は0.6とした。
Water, aluminum powder and a surfactant were added to the main raw material mixture and kneaded to prepare a slurry. At this time, slurries without addition of dimethylpolysiloxane in which all side chains were methyl groups (Conventional Example 1) and slurries with addition (Examples 1 to 7 and Comparative Examples 1 to 3) were prepared. The amount of addition to the slurry was 0.0005% by weight (Comparative Example 1), 0.001% by weight (Example 1), 0.005% by weight.
% By weight (Example 2), 0.01% by weight (Example 3),
0.05% by weight (Example 4), 0.10% by weight (Example 5), 0.15% by weight (Example 6), 0.18% by weight
(Example 7), 0.20% by weight (Comparative Example 2) and 0.1% by weight.
30 wt% (Comparative Example 3). The water / solid ratio (weight) was 0.6.

【0018】スラリーが石灰質原料の水和により硬化し
た後、185℃、11気圧のオートクレーブにおいて高
温高圧水蒸気養生を6時間施した。
After the slurry was hardened by hydration of the calcareous raw material, it was subjected to high-temperature and high-pressure steam curing in an autoclave at 185 ° C. and 11 atm for 6 hours.

【0019】作製したALCのサンプルについて、
(1)耐炭酸化性および(2)吸水性を調べた。
About the prepared ALC sample,
(1) Carbonation resistance and (2) water absorption were examined.

【0020】(1)耐炭酸化性 厚み10mm・高さ40mm・長さ80mmの大きさに
サンプルを成形し、促進炭酸化試験に供した。促進炭酸
化試験では、20℃、相対湿度90%、炭酸ガス濃度3
体積%の一定雰囲気下で20日間放置した。各サンプル
の炭酸化度を算出し、炭酸化度から耐炭酸化指数を算出
した。炭酸化度および耐炭酸化指数の算出式は次の通り
である。
(1) Carbonation Resistance A sample was formed into a size of 10 mm in thickness, 40 mm in height and 80 mm in length, and subjected to an accelerated carbonation test. In the accelerated carbonation test, the temperature was 20 ° C., the relative humidity was 90%, and the carbon dioxide concentration was 3
It was left for 20 days under a constant atmosphere of volume%. The degree of carbonation of each sample was calculated, and the carbonation resistance index was calculated from the degree of carbonation. Formulas for calculating the degree of carbonation and the index of resistance to carbonation are as follows.

【0021】炭酸化度(%)={(C−Co)/(Cm
ax−Co)}×100 ここで、Cはサンプルの二酸化炭素結合量(重量)、C
oは促進炭酸化試験未実施のサンプルの二酸化炭素結合
量であり、C、Coともに600〜800℃における炭
酸ガスへの分解による二酸化炭素減少量(重量)を熱分
析で測定した。また、Cmaxはサンプル中のカルシウ
ムがすべて炭酸カルシウムとなった場合の二酸化炭素結
合量で、サンプル中のカルシウム含有量を分析して計算
した。
Carbonation degree (%) =) (C-Co) / (Cm
ax-Co)} × 100 where C is the carbon dioxide binding amount (weight) of the sample, C
o is the amount of carbon dioxide binding of the sample which has not been subjected to the accelerated carbonation test, and the amount of reduction (weight) of carbon dioxide due to decomposition into carbon dioxide at 600 to 800 ° C. for both C and Co was measured by thermal analysis. Cmax is the amount of carbon dioxide bound when all of the calcium in the sample becomes calcium carbonate, and was calculated by analyzing the calcium content in the sample.

【0022】耐炭酸化指数=(従来例1の炭酸化度)/
(サンプルの炭酸化度) 算出した耐炭酸化指数が大きいほど、耐炭酸化性が優れ
ることになる。結果を表1に示す。
Carbonation resistance index = (degree of carbonation of Conventional Example 1) /
(Degree of Carbonation of Sample) The larger the calculated index of carbonation resistance, the better the carbonation resistance. Table 1 shows the results.

【0023】耐炭酸化性の判定は、耐炭酸化指数が1.
5未満を「不適」と、1.5以上・2.0未満を「可」
と、2.0以上を「適」とした。結果を表1に示す。表
1中、「不適」を△印で、「可」を○印で、「適」を◎
印で示した。
The determination of carbonation resistance is as follows:
"Unsuitable" for less than 5 and "OK" for 1.5 or more and less than 2.0
And 2.0 or more was regarded as “suitable”. Table 1 shows the results. In Table 1, "unsuitable" is indicated by a triangle, "acceptable" is indicated by a circle, and "appropriate" is indicated by ◎.
Indicated by the mark.

【0024】(2)吸水性 辺の長さが100mmの立方体の形状にサンプルを成形
し、全面吸水率を測定した。測定では、70℃の乾燥機
中で恒量となったサンプルを温度20±2℃の水中に2
4時間全面浸漬した。なお、サンプルを浸漬する際、発
泡方向を上に向け、上面の位置を水面下30mmにし
た。その後、各サンプルの全面吸水率(体積増加率)を
次式によって算出した。
(2) Water Absorption A sample was formed into a cubic shape having a side length of 100 mm, and the overall water absorption was measured. In the measurement, the sample which became constant weight in a 70 ° C. drier was placed in water at a temperature of 20 ± 2 ° C.
The whole surface was immersed for 4 hours. When the sample was immersed, the foaming direction was directed upward, and the upper surface was positioned 30 mm below the water surface. Thereafter, the overall water absorption (volume increase) of each sample was calculated by the following equation.

【0025】全面吸水率(体積%)={(V−Vo)/
Vo}×100 ここで、Vは24時間浸漬後のサンプルの体積、Voは
浸漬前(初期)のサンプルの体積(1000cm3 )で
ある。
Total water absorption (volume%) = {(V−Vo) /
Vo} × 100 Here, V is the volume of the sample after immersion for 24 hours, and Vo is the volume (1000 cm 3 ) of the sample before immersion (initial).

【0026】算出した全面吸水率が大きいほど、吸水性
が優れることになる。結果を表1に示す。
The higher the calculated total water absorption, the better the water absorption. Table 1 shows the results.

【0027】吸水性の判定は、全面吸水率が18体積%
未満を「不適」と、18体積%以上・20体積%未満を
「可」と、20体積%以上を「適」とした。結果を表1
に示す。表1中、「不適」を△印で、「可」を○印で、
「適」を◎印で示した。
The determination of water absorption was made by determining that the total water absorption was 18% by volume.
Less than 18% by volume and less than 20% by volume was considered as "Poor", and less than 20% by volume was "Appropriate". Table 1 shows the results
Shown in In Table 1, "Inappropriate" is indicated by a triangle, "OK" is indicated by a circle,
“Appropriate” is indicated by a mark ◎.

【0028】[0028]

【表1】 [Table 1]

【0029】表1から次のことが分かる。The following can be seen from Table 1.

【0030】(1)側鎖がすべてメチル基であるジメチ
ルポリシロキサンの添加量が0.001〜0.18重量
%(実施例1〜7)では、通常のALC(従来例1)に
比べて耐炭酸化性が著しく優れ、吸水性が同等程度であ
る。
(1) When the addition amount of dimethylpolysiloxane in which all the side chains are methyl groups is 0.001 to 0.18% by weight (Examples 1 to 7), compared with ordinary ALC (Conventional Example 1), Excellent carbonation resistance and comparable water absorption.

【0031】(2)側鎖がすべてメチル基であるジメチ
ルポリシロキサンの添加量が0.0005重量%(比較
例1)では耐炭酸化性が不十分であり、0.20重量%
(比較例2)および0.30重量%(比較例3)では吸
水性が不十分である。
(2) When the amount of dimethylpolysiloxane in which all side chains are all methyl groups is 0.0005% by weight (Comparative Example 1), the carbonation resistance is insufficient, and the amount is 0.20% by weight.
(Comparative Example 2) and 0.30% by weight (Comparative Example 3) have insufficient water absorption.

【0032】[0032]

【発明の効果】本発明によれば、耐炭酸化性に優れるた
めに耐劣化・耐久性に優れ、かつ撥水性ALCに多く見
られる凍害現象が吸水性が十分であるために起こらない
ALCを提供することができる。従って、ALC建築物
の耐用年数の延長や、補修・改修費用の低減を可能に
し、ひいては産業廃棄物量の低減という社会的な要請に
も応えることができる。
According to the present invention, an ALC which is excellent in deterioration resistance and durability due to excellent carbonation resistance and which does not cause the frost damage phenomenon often observed in water repellent ALC due to sufficient water absorption. Can be provided. Therefore, it is possible to extend the service life of the ALC building, reduce the cost of repair and repair, and meet social demands for reducing the amount of industrial waste.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 珪酸質成分および石灰質成分を主成分と
する軽量気泡コンクリートにおいて、側鎖がすべてメチ
ル基であるジメチルポリシロキサンを0.001〜0.
18重量%含むことを特徴とする耐炭酸化性に優れた軽
量気泡コンクリート。
1. A lightweight cellular concrete mainly composed of a siliceous component and a calcareous component, wherein 0.001 to 0.
Lightweight cellular concrete excellent in carbonation resistance characterized by containing 18% by weight.
JP2437199A 1998-12-14 1999-02-01 Lightweight aerated concrete excellent in carbonation resistance Pending JP2000219558A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2437199A JP2000219558A (en) 1999-02-01 1999-02-01 Lightweight aerated concrete excellent in carbonation resistance
AU60066/99A AU6006699A (en) 1998-12-14 1999-10-08 Light-weight cellular concrete with excellent carbonatization resistance
EP99973406A EP1055648A4 (en) 1998-12-14 1999-10-08 Light-weight cellular concrete with excellent carbonatization resistance
PCT/JP1999/005585 WO2000035827A1 (en) 1998-12-14 1999-10-08 Light-weight cellular concrete with excellent carbonatization resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2437199A JP2000219558A (en) 1999-02-01 1999-02-01 Lightweight aerated concrete excellent in carbonation resistance

Publications (1)

Publication Number Publication Date
JP2000219558A true JP2000219558A (en) 2000-08-08

Family

ID=12136344

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2437199A Pending JP2000219558A (en) 1998-12-14 1999-02-01 Lightweight aerated concrete excellent in carbonation resistance

Country Status (1)

Country Link
JP (1) JP2000219558A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100496646B1 (en) * 2001-06-26 2005-06-22 주식회사 리폼시스템 Lightweight foaming concreat

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100496646B1 (en) * 2001-06-26 2005-06-22 주식회사 리폼시스템 Lightweight foaming concreat

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