JPS58190854A - Coating material for low temperature liquid tank supporting wall - Google Patents
Coating material for low temperature liquid tank supporting wallInfo
- Publication number
- JPS58190854A JPS58190854A JP7414082A JP7414082A JPS58190854A JP S58190854 A JPS58190854 A JP S58190854A JP 7414082 A JP7414082 A JP 7414082A JP 7414082 A JP7414082 A JP 7414082A JP S58190854 A JPS58190854 A JP S58190854A
- Authority
- JP
- Japan
- Prior art keywords
- water
- cement
- coating material
- divalent
- liquid tank
- 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
- 239000000463 material Substances 0.000 title claims description 15
- 239000007788 liquid Substances 0.000 title claims description 12
- 239000011248 coating agent Substances 0.000 title claims description 7
- 238000000576 coating method Methods 0.000 title claims description 7
- 239000004568 cement Substances 0.000 claims description 13
- 229910052751 metal Inorganic materials 0.000 claims description 11
- 239000002184 metal Substances 0.000 claims description 11
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 238000005187 foaming Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 239000004113 Sepiolite Substances 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 229910052625 palygorskite Inorganic materials 0.000 claims description 3
- 235000021317 phosphate Nutrition 0.000 claims description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 3
- 229910052624 sepiolite Inorganic materials 0.000 claims description 3
- 235000019355 sepiolite Nutrition 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 239000011787 zinc oxide Substances 0.000 claims description 3
- 239000006229 carbon black Substances 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 239000004088 foaming agent Substances 0.000 claims description 2
- 229910044991 metal oxide Inorganic materials 0.000 claims description 2
- 150000004706 metal oxides Chemical class 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 239000010445 mica Substances 0.000 claims description 2
- 229910052618 mica group Inorganic materials 0.000 claims description 2
- 239000000741 silica gel Substances 0.000 claims description 2
- 229910002027 silica gel Inorganic materials 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 2
- 239000000454 talc Substances 0.000 claims description 2
- 229910052623 talc Inorganic materials 0.000 claims description 2
- 229920003169 water-soluble polymer Polymers 0.000 claims description 2
- 229910021536 Zeolite Inorganic materials 0.000 claims 1
- 150000001642 boronic acid derivatives Chemical class 0.000 claims 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 1
- 239000000428 dust Substances 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 239000010457 zeolite Substances 0.000 claims 1
- 239000006260 foam Substances 0.000 description 10
- 230000005484 gravity Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000004567 concrete Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 4
- 239000004115 Sodium Silicate Substances 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000009415 formwork Methods 0.000 description 3
- 229910052911 sodium silicate Inorganic materials 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000011398 Portland cement Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- MLIREBYILWEBDM-UHFFFAOYSA-N cyanoacetic acid Chemical compound OC(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-N 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- 229910001562 pearlite Inorganic materials 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- -1 ze-lite Substances 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 206010062717 Increased upper airway secretion Diseases 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N Li2O Inorganic materials [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000011401 Portland-fly ash cement Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000011083 cement mortar Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 239000006063 cullet Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 1
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011507 gypsum plaster Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 208000026435 phlegm Diseases 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000011863 silicon-based powder Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000006557 surface reaction Methods 0.000 description 1
- OMSYGYSPFZQFFP-UHFFFAOYSA-J zinc pyrophosphate Chemical compound [Zn+2].[Zn+2].[O-]P([O-])(=O)OP([O-])([O-])=O OMSYGYSPFZQFFP-UHFFFAOYSA-J 0.000 description 1
Landscapes
- Filling Or Discharging Of Gas Storage Vessels (AREA)
- Porous Artificial Stone Or Porous Ceramic Products (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、低温被覆抵抗の優れた低温成体タンク保持壁
用被覆材に係る。また、本発明は、係る液体が可燃性で
あって仮りに燃焼した時には頗る良好な耐火断熱性能を
発揮する画期的な被覆材を提供しようとするものである
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coating material for retaining walls of a low-temperature formed tank that has excellent low-temperature coating resistance. Furthermore, the present invention aims to provide an innovative coating material that exhibits extremely good fireproof and heat-insulating performance even if the liquid is flammable and burns.
従来より、液体酸素、液体窒素、LPG、 LNGなど
のごとき低温液体の貯蔵タンクの保護壁として相当幅の
厚いコンクリートが用いられている。該コンクリートは
擁壁の構築材としては非常に役立つが、万−低Ai1体
がタンクから漏出した時あるいは漏出と同時に燃焼した
時には急激な温度変化を受けて亀裂や爆裂などを生じて
外部に醐出し易い為、その内面に被覆材を施工したり、
工法的にコンクリートブロックをサンドイツチ材兼型枠
としてその空間部にコンクリ−1へを流し込んだりして
いる。しかしながら、係るコンクリートブロックや従来
からの被豹材はこのような用途として適当なものは極め
て少なく、例えば有機質断熱材は火災時の危険が大きく
、又軽量モルタルなとのごとき煕機質被覆月は低温破壊
が生じ易く且つ断熱性も左程良くないという欠点があっ
た。Traditionally, considerable widths of thick concrete have been used as protective walls for storage tanks for cryogenic liquids such as liquid oxygen, liquid nitrogen, LPG, LNG, etc. This concrete is very useful as a construction material for retaining walls, but when a single piece of low-Ai leaks from a tank or combusts at the same time as it leaks, the sudden temperature change causes cracks and explosions, causing it to leak to the outside. Because it is easy to take out, a covering material is applied to the inner surface,
In terms of construction methods, concrete blocks are used as sandwich materials and formwork, and concrete 1 is poured into the space. However, there are very few such concrete blocks or conventional covering materials that are suitable for such uses.For example, organic insulation materials are highly dangerous in the event of a fire, and lightweight mortar and other materials coated with organic materials are not suitable for such uses. It had the drawbacks of being prone to low-temperature breakdown and not having as good insulation properties.
本発明は、上記の欠点を厄く解決し得るもので、低温液
体タンクの保持壁の内面に特定の発泡体を施工すること
によって目的を達成したものである。The present invention makes it possible to overcome the above-mentioned disadvantages and achieves the object by applying a specific foam to the inner surface of the retaining wall of a cryogenic liquid tank.
即ち、本発明は、低温液体タンク保持壁の内面に特定の
発泡体の成形板を取り付ける又は発泡体を形成し得る組
成物を液体で施工する為の新しい被覆材に係り、(A)
■−23°Cにおけるam定数(pKa)がグ、0以下
である酸のpH/、3以下の水溶液と、無水アルカリ硅
酸塩及びセメントから選ばれる少くとも一種の塩基性を
有する鎖酸の硬化剤、又は■水可溶性アルカリ硅酸塩と
、セメント、シリカダスト、酸化亜鉛、I!+1級脂肪
酸の二価以1の金属塩、カルボキシル基を有する水溶性
高分子物質の二価以上の金属塩、酸性金属酸化物、リン
酸塩、二価金属の硫酸塩又は亜硫酸塩及びホウ酸塩から
選ばれる少くとも一種である水可溶性アルカリ硅酸塩の
硬化剤である!成分系反応性硬化性成分(以下(A)成
分という。)、(B)金属系発泡剤(以下(B)成分と
いう。)、及び(C)ジオ
リカゲル、ゼ・ライト、活性炭、カーボンブラック、タ
ルク、マイカ、パリゴルスカイト及びセピオライト並び
に界面活性剤から選ばれる少くとも一種の発泡安定剤(
以下(C)成分という。)を要
主中構成成分とするものである。That is, the present invention relates to a new coating material for attaching a molded plate of a specific foam to the inner surface of a cryogenic liquid tank retaining wall or for applying a composition capable of forming a foam with a liquid, (A)
■ An aqueous solution of an acid with an am constant (pKa) of 0 or less at -23°C and a pH of 3 or less, and a chain acid having at least one type of basicity selected from anhydrous alkali silicates and cement. Hardening agent, or ■ water-soluble alkali silicate, cement, silica dust, zinc oxide, I! + Divalent or higher valent metal salts of primary fatty acids, divalent or higher valent metal salts of water-soluble polymer substances having carboxyl groups, acidic metal oxides, phosphates, sulfates or sulfites of divalent metals, and boric acid It is a hardening agent for water-soluble alkali silicates, which is at least one type of salt! Component system: Reactive curable component (hereinafter referred to as component (A)), (B) metallic foaming agent (hereinafter referred to as component (B)), and (C) diorica gel, ze-lite, activated carbon, carbon black, talc. , mica, palygorskite and sepiolite, and at least one foaming stabilizer selected from surfactants (
Hereinafter, it will be referred to as component (C). ) is the main component.
本発明の被勘材の構成成分について若干説明する。 (
A)成分の二成分系反応硬化性組成物は2種あり、前述
のΦの系は酸−塩基液面反応、又■の系は水可溶性アル
カリ硅酸塩ゲル凝結反応によって硬化するものと想定さ
れる。■の系の酸としン酸・・・・・・、ピロリン酸亜
鉛等の酸性リン酸塩、ギ酸、グリコール酸、シアノ酢酸
等の有機酸が例示できる。■の系の酸の硬化剤としては
水ガラスカレットのごとき無水アルカリ硅酸塩とポルト
ランドセメント、フライアッシュセメント、アルミナセ
メント等のセメントが例示でき、これらの内の少くとも
/Nを用いる。次に、■の系の水可溶性アルカリ硅酸塩
としては、Li2O・5i02、Na2O・5102、
(NH4) 20 ・5j02なとのものが例示でき必
ず水可溶性を有しているものとする。又■の系の水可溶
性アルカリ硅酸塩の硬化剤は上に具体的に列挙している
ものが用いられる。以とのようなの又はOの系の(A)
成分と、金属単体、金属間化合物又は合金の粉体である
(B)成分と、上記に具体的に列挙した成分の粉体又は
液体である(C)成分とを水を介して−たんペースト状
にすると、混合物は時間の経過と共に、発泡を開始し、
発泡終了後は漸次硬化し初める。係る反応はその配合成
分の種類や量によっても異なるが、通常常温下で5〜乙
O分で発泡を開始し、遅くとも2I1時間後には完全硬
化終了するものである。The constituent components of the material to be treated according to the present invention will be briefly explained. (
There are two types of two-component reactive curable compositions of component A), and the system Φ mentioned above is assumed to be cured by an acid-base liquid surface reaction, and the system 2 is cured by a water-soluble alkali silicate gel coagulation reaction. be done. Examples of acids of the type (2) include phosphoric acid, acidic phosphates such as zinc pyrophosphate, and organic acids such as formic acid, glycolic acid, and cyanoacetic acid. Examples of the acid curing agent of the system (2) include anhydrous alkali silicates such as water glass cullet, and cements such as Portland cement, fly ash cement, and alumina cement, among which at least /N is used. Next, as the water-soluble alkali silicates of the system (■), Li2O.5i02, Na2O.5102,
(NH4) 20 .5j02 is an example, and it is assumed that it is always water-soluble. As the water-soluble alkali silicate curing agent of the system (2), those specifically listed above can be used. (A) of the series of or O such as
Component (B), which is a powder of an elemental metal, an intermetallic compound, or an alloy, and component (C), which is a powder or liquid of the components specifically listed above, are mixed into a phlegm paste through water. As time passes, the mixture begins to foam,
After foaming is completed, it gradually begins to harden. Although such a reaction varies depending on the types and amounts of the ingredients, foaming usually starts in 5 to 20 minutes at room temperature, and complete curing is completed after 21 hours at the latest.
上記被覆材を低温液体タンクの保持警に施工するに際し
、上記(A)〜(C)成分を予め成形用型枠内で混合し
て注入し発泡硬化せしめた成形板の形状で構allに貼
付又は取付ける方法、構造壁に型枠を取付けその中空部
に(A)〜(C)成分のペーストを注入する方法、構造
壁に直接又はラスなどを介して(A)〜(C)成分のペ
ーストを吹付けやコテなどによって塗付する方法など自
由に選択できる。こうして構造壁に無機質発泡体が被覆
された後は、被覆材をそのままにする他、耐久性や耐候
性を考慮して被覆材の表面に保護塗材を被覆し、又は被
覆材の表面に保護シートや板などを被覆し、もしくは耐
久性型枠をそのままにしておく装
ことなどを通じで保持壁内面の美・と保護をはかること
もできるのである。When applying the above-mentioned coating material to the holding guard of a low-temperature liquid tank, the above-mentioned components (A) to (C) are mixed and injected in a molding frame in advance, and then foamed and hardened to form a molded plate and affixed to all the structures. Or, a mounting method, a method of attaching a formwork to a structural wall and injecting the paste of the components (A) to (C) into the hollow part, a method of injecting the paste of the components (A) to (C) into the structural wall directly or through a lath, etc. You can freely choose how to apply it, such as by spraying or using a trowel. After the inorganic foam is coated on the structural wall in this way, in addition to leaving the covering material as it is, the surface of the covering material is coated with a protective coating material to ensure durability and weather resistance, or the surface of the covering material is protected. The beauty and protection of the inner surface of the retaining wall can be achieved by covering it with sheets or boards, or by leaving the durable formwork as it is.
このようにして得られる低温液体タンク保持用壁は、実
験を違嗜通してよく分かったのであるが低温下での安定
性が良好で且つ火災や高熱に対してもよく耐えるので、
構造壁の亀裂や爆裂を生ずることがなく防災上の性能向
上と共に防災技術の向上にも大いに役立つのである。The cryogenic liquid tank retaining wall obtained in this way has been found through extensive experiments to have good stability at low temperatures and to withstand fire and high heat.
This will not cause cracks or explosions in the structural walls, and will greatly help improve disaster prevention performance as well as disaster prevention technology.
以下実験を示す。The experiment is shown below.
実I@1(凍結融解試wり
以下に示す試料/〜10を切断又はvM合成形して寸法
200×700X30mmの供試体を得た。Sample I@1 (freeze-thaw test) Samples/~10 shown below were cut or molded into vM composite shapes to obtain specimens with dimensions of 200 x 700 x 30 mm.
これらの供試体を二週間常温下で空気養生した後IlO
°Cの恒温水帽に30分間浸漬する工程と、液体9素の
入ったジ゛ユワー組(直径200mm、深さ500mm
)に約3分間浸漬する工程とから成るサイクル凍結融解
試験を5サイクル行った所、各サイクル後における供試
体は第1表に示すようになった。After curing these specimens in air at room temperature for two weeks, IlO
A process of immersion in a constant-temperature water cap at
) A cyclic freeze-thaw test consisting of a step of immersing the sample in water for about 3 minutes was conducted for 5 cycles, and the specimens after each cycle were as shown in Table 1.
試m 1 : 5i02/ Na2Oモル比!、/の無
水硅酸ソーダ100重′1に部、オルトリン酸アルミニ
ウム(濃度30%730重量部、金属硅素粉2重量部及
びシリカゲル粉S重!部を混合して製造。発泡体の比重
は0.35になった。Trial m1: 5i02/Na2O molar ratio! Produced by mixing 1 part by weight of anhydrous sodium silicate, 730 parts by weight of aluminum orthophosphate (concentration 30%, 2 parts by weight of metal silicon powder, and 1 part by weight of silica gel powder. The specific gravity of the foam is 0. It became .35.
試料2 : S+02/ Na2Oモル比2.5の硅酸
ソーダ(濃度30%)700重を部、アルミナセメント
<zoits、ポルトランドセメント70重量部、Fe
5t粉3重量部及びパリゴルスカイト粉5重散部を混合
して製造。Sample 2: 700 parts by weight of sodium silicate (concentration 30%) with S+02/Na2O molar ratio of 2.5, alumina cement <zoits, 70 parts by weight of Portland cement, Fe
Manufactured by mixing 3 parts by weight of 5t powder and 5 parts by weight of palygorskite powder.
発泡体の比重は0.35になった。The foam had a specific gravity of 0.35.
試料3 : 5i02/ Na2Oモル比2.0の硅酸
ソーダ(濃度30%)700重1部、pesiWM時に
副生された5i0293%のシリカダスト ゛10重
散部、酸化亜鉛lON散部、金属アルミニウム2重量部
及びセピオライト乙重量部を混合して製造。発泡体の比
重は0.57になった。Sample 3: 700 parts by weight of sodium silicate (concentration 30%) with a 5i02/Na2O molar ratio of 2.0, 10 parts by weight of 5i0293% silica dust by-produced during pesiWM, 10 parts dispersed in zinc oxide lON, metal aluminum Manufactured by mixing 2 parts by weight and 2 parts by weight of sepiolite. The specific gravity of the foam was 0.57.
試14: JIS A 9510に規定の硅酸カルシウ
ム保温板7号で比重0.230
試料5:標準セメントモルタル板(セメント1対標準砂
3)で比重2.0゜
試a、 6 : JIS A 6904に規定のボード
川石こうプラスターで比@0.90゜
試料7 : JIS A 5416 ニ規定ノALcテ
比重0.3K。Test 14: Calcium silicate heat insulation board No. 7 specified in JIS A 9510, specific gravity 0.230 Sample 5: Standard cement mortar board (1 cement to 3 standard sand), specific gravity 2.0° Test a, 6: JIS A 6904 Specimen 7: JIS A 5416 JIS A 5416 standard Gypsum plaster with a specific gravity of 0.3K.
試料8:ボルトランドセメント1oox…部、金属アル
ミニウム1重量部、ポリビニルアルコール/重量部及び
水50重量部を混合して製造したセメント発泡体で比重
0.73である。−
試料9:ボルトランドセメントノ00重景部、金属アル
ミニウム粉0./重量部及び水
50重量部を混合して製造したセメント発泡体で比重0
.乙Sである。Sample 8: A cement foam manufactured by mixing 100 parts of Boltland cement, 1 part by weight of aluminum metal, part by weight of polyvinyl alcohol, and 50 parts by weight of water, and has a specific gravity of 0.73. - Sample 9: Boltland cement 00 heavy area, metal aluminum powder 0. / parts by weight and 50 parts by weight of water to produce a cement foam with a specific gravity of 0.
.. This is Otsu S.
試料10:ボルトランドセメント700重量部、水50
重量部及び発泡パーライト20重量部を混合して製造し
たパーライト−モルタルで比重/、/2である。Sample 10: 700 parts by weight of Boltland cement, 50 parts by weight of water
Perlite-mortar produced by mixing 20 parts by weight of foamed pearlite and 20 parts by weight of foamed pearlite has a specific gravity of /, /2.
第 / 表 サイク、。Chapter / Table Psych,.
/23113
試料1 00000
試料2 00000
試料 3 00000
試料 4 X −−−−−
試料 5 00 △ × −
試料6 0 ×−m−
※○印は全く興状ないΔ印は表面へアークラック、X印
は割れ発生、−印は試験続行不能を意味する。/23113 Sample 1 00000 Sample 2 00000 Sample 3 00000 Sample 4 indicates that a crack has occurred, and a - symbol indicates that the test cannot be continued.
実験2 (加熱試験)
実験1の方法に従って、寸法200X200X100n
mの供試体10個を得た。これらの供試体を二週間常温
下で空気養生した径、幅100mmの両側に熱電対を設
置いその一方を1ooo〜/100℃に維持されたLP
Gガスバーナーを当て、他方(裏面)を耐火断熱レンガ
で保温し、g時間加熱後の裏面温度上昇を測定したとこ
ろ、第2表に示す結果が得られた。Experiment 2 (heating test) According to the method of Experiment 1, the dimensions were 200x200x100n.
Ten specimens of m were obtained. These specimens were air-cured at room temperature for two weeks, and thermocouples were installed on both sides of the diameter and width of 100 mm, and one side was maintained at 1ooo~/100℃.
A G gas burner was applied, the other side (back side) was kept warm with a fireproof insulating brick, and the temperature rise on the back side after heating for g hours was measured, and the results shown in Table 2 were obtained.
第2表 以上 特許出願人 四国化研工業株式会社 / /Table 2 that's all Patent applicant Shikoku Kaken Kogyo Co., Ltd. / /
Claims (1)
硬化組成物: 025°Cにおける電w1定数(pKa) ff111
.0以下である酸のpH/=5以下の水溶液へ無水アル
カリ硅酸塩及びセメントから選ばれる少くとも一種の塩
基性を有する鎖酸の硬化剤、 ■ 水可溶性アルカリ硅酸塩と、セメント、シリカダス
ト、酸化亜鉛、高級脂肪酸の二価以上の金属塩、カルボ
キシル基を有する水溶性高分子物質の二価以上の金属塩
、酸性金属酸化物、リン酸塩、二価金属の硫酸塩又は亜
硫酸塩及びホウ酸塩から選ばれる少くとも一種である水
可溶性アルカリ硅酸塩の硬化剤、 (B)金属系発泡剤、および (C)シリカゲル、ゼオライト、活性炭、カーボンブラ
ック、タルク、マイカ、パリゴルスカイト、セピオライ
ト及び界面活性剤から選ばれる少くとも一種の発泡安定
剤、 を主要構成成分とする低温液体タンク保持壁用被覆材。[Claims] 1. (, A) A two-component reaction-curing composition having ■ or Φ as described below: Electrical w1 constant (pKa) at 025°C ff111
.. A curing agent of a chain acid having at least one type of basicity selected from anhydrous alkali silicates and cement; ■ water-soluble alkali silicates, cement, and silica; Dust, zinc oxide, divalent or higher valent metal salts of higher fatty acids, divalent or higher valent metal salts of water-soluble polymer substances having carboxyl groups, acidic metal oxides, phosphates, sulfates or sulfites of divalent metals and at least one type of water-soluble alkali silicate curing agent selected from borates, (B) a metal foaming agent, and (C) silica gel, zeolite, activated carbon, carbon black, talc, mica, palygorskite, sepiolite. A coating material for a retaining wall of a low-temperature liquid tank, the main component being at least one foaming stabilizer selected from surfactants and surfactants.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7414082A JPS58190854A (en) | 1982-05-01 | 1982-05-01 | Coating material for low temperature liquid tank supporting wall |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7414082A JPS58190854A (en) | 1982-05-01 | 1982-05-01 | Coating material for low temperature liquid tank supporting wall |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS58190854A true JPS58190854A (en) | 1983-11-07 |
Family
ID=13538572
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7414082A Pending JPS58190854A (en) | 1982-05-01 | 1982-05-01 | Coating material for low temperature liquid tank supporting wall |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58190854A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6497945B1 (en) * | 1999-03-02 | 2002-12-24 | Peter Niedner | Foamlike mineral building and structural material as well as a method of producing a mineral foam and an apparatus for carrying out this method |
-
1982
- 1982-05-01 JP JP7414082A patent/JPS58190854A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6497945B1 (en) * | 1999-03-02 | 2002-12-24 | Peter Niedner | Foamlike mineral building and structural material as well as a method of producing a mineral foam and an apparatus for carrying out this method |
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