JPS58140356A - Lining material - Google Patents
Lining materialInfo
- Publication number
- JPS58140356A JPS58140356A JP1916882A JP1916882A JPS58140356A JP S58140356 A JPS58140356 A JP S58140356A JP 1916882 A JP1916882 A JP 1916882A JP 1916882 A JP1916882 A JP 1916882A JP S58140356 A JPS58140356 A JP S58140356A
- Authority
- JP
- Japan
- Prior art keywords
- lining material
- resistance
- sodium silicate
- blast furnace
- furnace slag
- 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
Landscapes
- 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】
本発明はライニング材、詳しくは、結合剤として、珪酸
ソーダと高炉水砕スラグとを併用し、高度な化学抵抗性
と耐熱性を有するライニング材に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a lining material, and more particularly to a lining material that uses sodium silicate and granulated blast furnace slag in combination as a binder and has high chemical resistance and heat resistance.
煙道、排煙の集塵装置、脱値装置、廃液処理槽、工業窯
炉、酸類を使用する工場の槽、床面、壁、ピット等のよ
うに苛酷□な条件下で使用される鉄板、コンクリート、
煉瓦等の基材の表面を保護するために、耐薬品性又は耐
熱性を有する材料でライニングすることが行なわれてい
る。Iron plates used under harsh conditions such as flues, exhaust gas dust collectors, devalue devices, waste liquid treatment tanks, industrial kilns, tanks in factories that use acids, floors, walls, pits, etc. ,concrete,
In order to protect the surface of a base material such as a brick, lining with a material having chemical resistance or heat resistance is performed.
従来より、ライニング材は、その結合剤の種類によって
、珪酸ノーダ系のものと七メント系のもがある。前者は
、耐酸性を有するがアルカリ性溶液や力スに弱く、逆に
、f&番は、アルカリに強いが酸に侵されやすいという
欠点がちるので、両者の欠点を解決するものとして、珪
酸ソーダとアルミナセメントを併用するものが提案され
ている(特開昭49−106524号公報)。 しかし
、このライニング材にあっても、耐酸性と耐熱性が十分
でなく、その改善が強く要望されている。Conventionally, lining materials have been classified into silicate-based materials and hepta-mention-based materials, depending on the type of binder used. The former has the disadvantage of being acid resistant but weak against alkaline solutions and force, and conversely, f& is strong against alkalis but easily attacked by acids.As a solution to the disadvantages of both, sodium silicate and It has been proposed to use alumina cement in combination (Japanese Unexamined Patent Publication No. 106524/1983). However, even this lining material does not have sufficient acid resistance and heat resistance, and there is a strong demand for improvement.
本発明者は、このような要望に応えるべく種々検討した
結果、珪酸ソーダとアルミナセメントを併用するライニ
ング材において、そのアルミナセメントの一部又は・全
部を、高炉水砕スラグ粉−未とそのアルカリ刺激剤から
なる結合剤に置きかえれば、すぐれた耐酸性と耐熱性を
付与できることを見い出し、本発明を完成したものであ
る。As a result of various studies to meet these demands, the inventor of the present invention found that, in a lining material that uses both sodium silicate and alumina cement, the alumina cement is partially or completely replaced with granulated blast furnace slag powder and its alkali. The present invention was completed based on the discovery that excellent acid resistance and heat resistance could be imparted by replacing the binder with a stimulant.
すなわち、本発明は、骨材、珪酸ソーダ、珪酸ソーダの
硬化促進剤、高炉水砕スラグ粉末、及びアルカリ刺激剤
を含有してなるライニング材である0
以t゛、詳しく本発明について説明する。That is, the present invention is a lining material comprising aggregate, sodium silicate, a hardening accelerator of sodium silicate, granulated blast furnace slag powder, and an alkali stimulant.The present invention will now be described in detail.
本発明において、骨材は、石英層粉末、石綿粉衣、カラ
ス粉末、珪砂粉末、カーボン粉末、セルベン、粘土質シ
ャモット、アルミナ質シャモット、バーミキュライト、
パーライト、抗火石、パミス等の耐酸性骨材や耐熱性骨
材の1を重または2種以Eが好適に使用される。In the present invention, the aggregates include quartz layer powder, asbestos powder, crow powder, silica sand powder, carbon powder, cerben, clayey chamotte, alumina chamotte, vermiculite,
Acid-resistant aggregates and heat-resistant aggregates such as perlite, anti-flinder stone, and pumice are preferably used.
珪酸ソーダとしては、メタ珪酸ソーダあるいは1号から
3号の珪酸ソーダ等の1踵以上が使用され、その割合は
、骨材100重喰部に対し5〜500重1部とするのが
好ましい。5型破部よりも少量では、ライニング材の強
度発現が憇くなり、また、soo ’t を部を著しく
こえて多く配合する利点はなく、反って、耐酸性と耐熱
性が小さくなる。強度発現と耐酸性の点から、メタ珪酸
ソーダと珪酸ソーダとを併用することは望ましいことで
ある。As the sodium silicate, at least one heel of sodium metasilicate or sodium silicate No. 1 to No. 3 is used, and the ratio thereof is preferably 5 to 1 part by weight per 100 parts by weight of the aggregate. If the amount is less than that of the 5-shaped broken part, the strength of the lining material will be poor, and there is no advantage in adding soo't in a significantly larger amount than that of the broken part, and the acid resistance and heat resistance will be reduced. From the viewpoint of strength development and acid resistance, it is desirable to use sodium metasilicate and sodium silicate together.
珪酸ソーダの硬化促進剤としては、従来より知られてい
るものでよく、具体例をあげれば、無機系のものとして
は、珪弗化ソーダ、珪弗化カリなどの珪弗化アルカリ、
珪酸カルシウム、燐酸アルミニウム、縮合燐酸アルミニ
ウム、など、有精系のものとしては、脂肪酸アミド、脂
肪酸エステルなどであり、なかでも、燐酸アルミニウム
又は縮合燐酸アルミニウムが好ましい。これらの硬化促
進剤の1種以上を、珪酸ソーダ100tIt部に対し1
0〜150重敗部程度1吏用する。As the curing accelerator for sodium silicate, conventionally known ones may be used. Specific examples include inorganic ones such as alkali silicate fluorides such as sodium silicate and potassium silicate fluoride,
Examples of seminal substances such as calcium silicate, aluminum phosphate, and condensed aluminum phosphate include fatty acid amides and fatty acid esters, and among them, aluminum phosphate and condensed aluminum phosphate are preferred. One or more of these curing accelerators should be added in an amount of 1 part per 100 tIt parts of sodium silicate.
0 to 150 heavy losses, use once.
高炉水砕スラグは、ライニング材に耐アルカリ性、耐酸
性などの化学抵抗性と耐熱性を付与するために必要な成
分であり、アルカリ刺激剤は、その水利反応を活性化さ
せて、早期に強度発現させるのに・必要なものである。Granulated blast furnace slag is a necessary component to impart chemical resistance such as alkali resistance and acid resistance to the lining material, as well as heat resistance, and the alkaline stimulant activates the water utilization reaction to quickly strengthen the lining material. It is necessary for it to manifest itself.
高炉水砕スラグは、鉄鋼製造時に副竜される通常のもの
が使用で゛き、粒径の細いもの程水和反応が早くなるの
で好ましいが、ブレーン比表面積で3 、000 cm
54もあれば十分である。高炉水砕スラグ粉末の使用量
は、骨材100重瞳部に対し5〜500重量部程度置部
る。5重喰部よりも少量では、ライニング材の強度発現
が悪くなり、また、500重綾都合著しくこえて配合す
る利点はなく、むしろ、化学抵抗性が減少する順向にな
る。As for the granulated blast furnace slag, it is possible to use ordinary granulated blast furnace slag that is used as a secondary product during steel manufacturing, and it is preferable that the granulated blast furnace slag has a smaller particle size because the hydration reaction is faster.
54 is sufficient. The amount of granulated blast furnace slag powder to be used is about 5 to 500 parts by weight per 100-weight pupil of the aggregate. If the amount is less than 5 parts, the strength of the lining material will be poor, and there is no advantage to mixing more than 500 parts, but rather the chemical resistance tends to decrease.
アルカリ刺激剤としては、アルカリ金属文゛はアルカリ
土類金属の水酸化物、炭酸塩、硫酸塩や、ポルトランド
セメントなどが[重用され、なかでも、水酸化ナトリウ
ムは、強アルカリでありかつ入手も容易なことから、工
業的に適したものである。As alkali stimulants, alkali metals such as alkaline earth metal hydroxides, carbonates, and sulfates, and Portland cement are used [in particular, sodium hydroxide is a strong alkali and is not readily available]. Since it is easy, it is suitable for industrial use.
さらには、水酸化ナトリウムと、炭酸ナトリーウム又は
炭酸水素すl−IJウムとを併用することにより、長期
強度の発現がよくなるので、それだけ耐久性の大きなラ
イニング材を■ンすることができるという利点がある。Furthermore, by using sodium hydroxide together with sodium carbonate or sodium bicarbonate, long-term strength can be improved, so there is the advantage that a lining material with greater durability can be made. be.
アルカリ刺激剤の使用量は、高炉水砕スラグ粉末100
’+tt部に対し3〜10重量部が好ましい。3重量部
よりも少1であると強度発現が悪く、10 重量部をこ
えても強度の伸びは期待できない。 ゛
以上の各成分からなるライニング材は、適歇の水が配合
されてモルタルとなし、それをライニングが必要となる
物品に施工し、硬化してから使用される。その際、ライ
ニングの各成分はあらかじめ混合したものを用いてもよ
く、また、水との混練時に混合してもよい。The amount of alkaline stimulant used is 100 ml of granulated blast furnace slag powder.
It is preferably 3 to 10 parts by weight based on the +tt parts. If the amount is less than 3 parts by weight, strength development will be poor, and if it exceeds 10 parts by weight, no increase in strength can be expected. The lining material consisting of each of the above components is mixed with appropriate amounts of water to form a mortar, applied to an article requiring lining, and cured before use. At this time, each component of the lining may be mixed in advance, or may be mixed at the time of kneading with water.
本発明のライニング材は、2撞頌の結合剤を1吏用して
いるので、水と混合すると、2つの硬化反応が同時に進
行する。従って、硬化時間や作業性はそれらの配合比を
変えることにより自由に調節できる。また、それらの結
合剤は、適曖の水を加えて混練し常温で硬化するもので
あるから任意の施工方法を採用することができる。Since the lining material of the present invention uses one part of a two-part binder, when mixed with water, two curing reactions proceed simultaneously. Therefore, the curing time and workability can be freely adjusted by changing their blending ratio. Moreover, since these binders are those that are mixed with water in an appropriate amount and harden at room temperature, any construction method can be employed.
また、本発明のライニング材に、5BIL、NBR。In addition, 5BIL and NBR are used as the lining material of the present invention.
C)L、EVAなどのラテ゛ンクスをへ己合すること1
こより、組織を緻密化し外部からの侵入を著しく抑え、
化学抵抗性をさらに高めるだけでなく、施工性、接着性
、耐クラツク性を向上させることができる。C) Combining latex such as L and EVA 1
This makes the organization more compact and significantly suppresses intrusion from the outside.
It not only further increases chemical resistance but also improves workability, adhesion, and crack resistance.
さらには、セメント減水剤(分散剤)やグルコン酸、ク
エン酸、酒石酸又はそれらの塩のような有機酸類を添加
することにより、流動性を高めることができ、また、ア
ルミナセメントを配合することにより、高温における耐
熱性を高めることができる。Furthermore, fluidity can be increased by adding cement water reducers (dispersants) and organic acids such as gluconic acid, citric acid, tartaric acid, or their salts, and by adding alumina cement. , heat resistance at high temperatures can be improved.
本発明品によれば、耐酸性と耐熱性を著しく高めたもの
にすることができ、しかも、この改良は、産業副産物で
ある高炉水砕スラグにより行な゛えたという点で有用な
ものである。According to the product of the present invention, it is possible to significantly improve acid resistance and heat resistance, and this improvement is useful in that it can be achieved using granulated blast furnace slag, which is an industrial by-product. .
以下、実施例をあげてさらに本発明を説明する。The present invention will be further explained below with reference to Examples.
実施例1
第1表に示す配合割合からなるライニング材1oott
部に水16重量部を加え、モルタルミキサーで攪拌混合
してモルタルとし、これを練瓦に5W+厚さにコテ塗り
ライニングし24時間放置した。このライニング物につ
いて、耐蝕性、せん断接着力、収縮率及びクランク発生
率を測定した。Example 1 Lining material 1ooott consisting of the compounding ratio shown in Table 1
16 parts by weight of water was added to the mixture and mixed with a mortar mixer to form a mortar, which was lined with a trowel to a thickness of 5W and left for 24 hours. Corrosion resistance, shear adhesive strength, shrinkage rate, and crank occurrence rate were measured for this lining product.
比較例として、珪酸ソーダとアルミナセメントを結合剤
とするものについても測定した。これらの結果を第1表
に示す。As a comparative example, measurements were also carried out using sodium silicate and alumina cement as binders. These results are shown in Table 1.
耐蝕性は、ライニング材表面を9D C110%硫酸水
溶液に6時間浸したときの重液減少率、せん断接着力と
収縮率は、500 Cで24時間放置後の測定値、クラ
ック発生は、500Cで2週間放置後の肉眼観察で示し
た。Corrosion resistance is determined by the heavy liquid reduction rate when the surface of the lining material is immersed in a 9D C110% sulfuric acid aqueous solution for 6 hours, the shear adhesive strength and shrinkage rate are measured values after being left at 500 C for 24 hours, and the occurrence of cracks is determined by the values measured at 500 C. This was shown by visual observation after being left for 2 weeks.
第 1 表
実施例2
第2表に示すライニング材で調合したモルタルを鉄板に
50厚にコテ塗りし、実施例1と同様な物性を測定した
。その結果を第2表に示す。Table 1 Example 2 Mortar prepared with the lining material shown in Table 2 was troweled to a thickness of 50 mm on an iron plate, and the same physical properties as in Example 1 were measured. The results are shown in Table 2.
耐蝕性は実施例1と同一条件、せん断接着力と収縮率は
、160Cで24時間放置後の測定イd、クラック発生
は、160 Cで2週間放置後の肉眼観察である。Corrosion resistance was measured under the same conditions as in Example 1, shear adhesive strength and shrinkage were measured after being left at 160 C for 24 hours, and crack occurrence was observed with the naked eye after being left at 160 C for 2 weeks.
第 2 表
以北のように、本発明品は耐蝕性、接着性、耐クラツク
性に優れ、幅云い分野に使用できるライニング材である
。As shown in Table 2, the product of the present invention has excellent corrosion resistance, adhesion, and crack resistance, and is a lining material that can be used in a wide variety of fields.
特許出願人 電気化学工業株式会社Patent applicant: Denki Kagaku Kogyo Co., Ltd.
Claims (1)
スラグ粉末、及びアルカリ刺激剤を含有してなるライニ
ング材。A lining material containing aggregate, sodium silicate, a sodium silicate hardening accelerator, granulated blast furnace slag powder, and an alkali stimulant.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1916882A JPS58140356A (en) | 1982-02-09 | 1982-02-09 | Lining material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1916882A JPS58140356A (en) | 1982-02-09 | 1982-02-09 | Lining material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58140356A true JPS58140356A (en) | 1983-08-20 |
JPH0338228B2 JPH0338228B2 (en) | 1991-06-10 |
Family
ID=11991830
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1916882A Granted JPS58140356A (en) | 1982-02-09 | 1982-02-09 | Lining material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58140356A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61178698A (en) * | 1985-02-05 | 1986-08-11 | 株式会社日立製作所 | Method of hardening water glass |
WO1989003370A1 (en) * | 1987-10-14 | 1989-04-20 | Simferopolsky Filial Dnepropetrovskogo Inzhenerno- | Composition for making artificial stone materials |
US4979990A (en) * | 1986-07-24 | 1990-12-25 | Fosroc International Limited | Foamable composition |
US5073198A (en) * | 1985-10-14 | 1991-12-17 | Kurz Fredrik W A | Method of preparing building materials |
US5082501A (en) * | 1985-10-14 | 1992-01-21 | Kurz Fredrik W A | Method of preparing building materials |
CN1049414C (en) * | 1994-02-05 | 2000-02-16 | 郝天成 | Light heat-insulation acid-proof building block for chimney and producing method thereof |
WO2000044685A1 (en) * | 1999-01-27 | 2000-08-03 | Weihua Jin | Inorganic binders employing waste glass |
JP2001163660A (en) * | 1999-09-29 | 2001-06-19 | Taiheiyo Cement Corp | Hardenable composition and hardened body |
EP1081114B2 (en) † | 1999-09-02 | 2005-08-03 | Heidelberger Bauchemie GmbH Marke Deitermann | Building Material Mixture |
JP2006193367A (en) * | 2005-01-13 | 2006-07-27 | Denki Kagaku Kogyo Kk | Hydraulic material |
EP1236702B2 (en) † | 2001-03-02 | 2011-08-10 | maxit Deutschland GmbH | Building material mixture containing waterglass |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4954442A (en) * | 1972-09-28 | 1974-05-27 | ||
JPS49106524A (en) * | 1973-02-09 | 1974-10-09 | ||
JPS5490223A (en) * | 1977-12-28 | 1979-07-17 | Mitsubishi Mining & Cement Co | Method of making lighttweight material |
JPS5857380A (en) * | 1981-09-10 | 1983-04-05 | ヘキスト・アクチエンゲゼルシヤフト | 9,10-substituted 2-mesitylimino-3-alkyl- 3,4,6,7-tetrahydro-2h-pyrimido(6,1-a)isoquinolin- 4-one |
-
1982
- 1982-02-09 JP JP1916882A patent/JPS58140356A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4954442A (en) * | 1972-09-28 | 1974-05-27 | ||
JPS49106524A (en) * | 1973-02-09 | 1974-10-09 | ||
JPS5490223A (en) * | 1977-12-28 | 1979-07-17 | Mitsubishi Mining & Cement Co | Method of making lighttweight material |
JPS5857380A (en) * | 1981-09-10 | 1983-04-05 | ヘキスト・アクチエンゲゼルシヤフト | 9,10-substituted 2-mesitylimino-3-alkyl- 3,4,6,7-tetrahydro-2h-pyrimido(6,1-a)isoquinolin- 4-one |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61178698A (en) * | 1985-02-05 | 1986-08-11 | 株式会社日立製作所 | Method of hardening water glass |
US5073198A (en) * | 1985-10-14 | 1991-12-17 | Kurz Fredrik W A | Method of preparing building materials |
US5082501A (en) * | 1985-10-14 | 1992-01-21 | Kurz Fredrik W A | Method of preparing building materials |
US4979990A (en) * | 1986-07-24 | 1990-12-25 | Fosroc International Limited | Foamable composition |
WO1989003370A1 (en) * | 1987-10-14 | 1989-04-20 | Simferopolsky Filial Dnepropetrovskogo Inzhenerno- | Composition for making artificial stone materials |
CN1049414C (en) * | 1994-02-05 | 2000-02-16 | 郝天成 | Light heat-insulation acid-proof building block for chimney and producing method thereof |
WO2000044685A1 (en) * | 1999-01-27 | 2000-08-03 | Weihua Jin | Inorganic binders employing waste glass |
US6296699B1 (en) * | 1999-01-27 | 2001-10-02 | Weihua Jin | Inorganic binders employing waste glass |
EP1081114B2 (en) † | 1999-09-02 | 2005-08-03 | Heidelberger Bauchemie GmbH Marke Deitermann | Building Material Mixture |
JP2001163660A (en) * | 1999-09-29 | 2001-06-19 | Taiheiyo Cement Corp | Hardenable composition and hardened body |
EP1236702B2 (en) † | 2001-03-02 | 2011-08-10 | maxit Deutschland GmbH | Building material mixture containing waterglass |
JP2006193367A (en) * | 2005-01-13 | 2006-07-27 | Denki Kagaku Kogyo Kk | Hydraulic material |
JP4567473B2 (en) * | 2005-01-13 | 2010-10-20 | 電気化学工業株式会社 | Hydraulic material |
Also Published As
Publication number | Publication date |
---|---|
JPH0338228B2 (en) | 1991-06-10 |
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