JPH03212477A - Flame-retardant sealing material - Google Patents
Flame-retardant sealing materialInfo
- Publication number
- JPH03212477A JPH03212477A JP945590A JP945590A JPH03212477A JP H03212477 A JPH03212477 A JP H03212477A JP 945590 A JP945590 A JP 945590A JP 945590 A JP945590 A JP 945590A JP H03212477 A JPH03212477 A JP H03212477A
- Authority
- JP
- Japan
- Prior art keywords
- pts
- sealing material
- weight
- flame
- liquid
- 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
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- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は各種分野で使用可能な、特に建築用として好適
な難燃性シーリング材に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a flame-retardant sealing material that can be used in various fields, and is particularly suitable for architectural use.
建築用のシーリング材としてウレタン系、アクリル系、
シリコン系などのものが布板されてし)るが、ウレタン
系やアクリル系のシーリング材は一般に難燃性に乏しく
、一方シリコン系のシーリング材は一般に耐候性、特に
カビによる黒汚染及びモルタル等に対する接着性が充分
でない等の問題がある。Urethane-based, acrylic-based,
However, urethane-based and acrylic-based sealants generally have poor flame retardancy, while silicone-based sealants generally have poor weather resistance, especially against black stains caused by mold and mortar. There are problems such as insufficient adhesion to.
本発明は、上記の事情を考慮して耐候性(カビによる黒
汚染)並びにモルタル等に対する接着性が良好で、しか
も難燃性、耐火性に優れたシーリング材を開発すること
を目的とする。In consideration of the above circumstances, the present invention aims to develop a sealing material that has good weather resistance (black staining due to mold) and adhesion to mortar, etc., and is also excellent in flame retardancy and fire resistance.
上記の問題点は、液状ポリクロロプレン、及び当該液状
ポリクロロブ1フ100重量部あたり50〜500重量
部の液状ポリウレタン、50〜500重量部の水和金属
酸化物とからなることを特徴とする難燃性シーリング材
によって解決される。The above problem is solved by the flame retardant, which is characterized by comprising liquid polychloroprene, 50 to 500 parts by weight of liquid polyurethane, and 50 to 500 parts by weight of hydrated metal oxide per 100 parts by weight of the liquid polychloroprene. This problem can be solved by using adhesive sealant.
本発明のシーリング材は、配合成分同士の相互作用によ
り耐候性、接着性、並びに難燃性が良好で、しかも所望
個所への施与後における大気中での自己硬化性が良好で
あって且つ燃焼しても燃焼後に於ける灰化物が燃焼前の
形態を略保持していて灰化状態でも耐火性並びに延防止
性を示す。The sealant of the present invention has good weather resistance, adhesion, and flame retardancy due to the interaction between the ingredients, and also has good self-curing properties in the atmosphere after being applied to a desired location. Even after combustion, the ash after combustion retains its pre-combustion form and exhibits fire resistance and spread prevention properties even in the ash state.
液状ポリクロロプレンとしては、たとえば数平均分子量
が約1 、000〜100,000 、特に3.500
〜10.000、室温におけるブルックフィールド粘度
が10.000〜200.OOOcp、特に30,00
0〜150,0Ocpの不揮発性液体状のものが使用さ
れ、就中末端又は分子中にヒドロキシル基を1個以上持
ったものが好ましい。As liquid polychloroprene, for example, a number average molecular weight of about 1,000 to 100,000, especially 3.500 is used.
~10.000, Brookfield viscosity at room temperature is 10.000~200. OOOcp, especially 30,00
A nonvolatile liquid having a concentration of 0 to 150.0 Ocp is used, and one having one or more hydroxyl groups at the end or in the molecule is particularly preferred.
液状ポリウレタンとしては、イソシアネートとポリオー
ルとからなる通常の二液型のものが例示される。その場
合、イソシアネートとポリオールとの重量比は、前者/
後者の比で0.5/]、、O〜2.0/1.0、好まし
くは0.7/1.0〜1.5/1.0の範囲が適当であ
る。イソシアネートとしては、トリレンジイソシアネー
ト、ジフヱニルメタンジイソシアネート、ヘキサメチレ
ンジイソシアネート、及び前記等のイソシアネートのウ
レタンプレポリマー等が用いられ、市販品ではEC26
10B(ポリウレタン化成社) 、UR[CN−202
3(伊藤製油社)が例示される。Examples of liquid polyurethanes include common two-component polyurethanes consisting of isocyanate and polyol. In that case, the weight ratio of isocyanate to polyol is the former/
The latter ratio is suitably in the range of 0.5/], 0 to 2.0/1.0, preferably 0.7/1.0 to 1.5/1.0. As the isocyanate, tolylene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate, and urethane prepolymers of the above-mentioned isocyanates are used, and commercially available products have EC26
10B (Polyurethane Kasei Co., Ltd.), UR [CN-202
3 (Ito Oil Co., Ltd.) is exemplified.
ポリオールとしては、低分子量ポリオール(エチレング
リコール、ジエチレングリコール、ジプロピレングリコ
ール、114−ブタンジオール等)、ポリエーテルポリ
オール(ポリエチレングリコール、ポリオキシプロピレ
ングリコール、エチレンオキシド−プロピレンオキシド
共重合体等)、ポリエステルポリオール(ポリβ−メチ
ル−δ−)へレロラクトン、ポリカプロラクトン、ジオ
ール二塩基酸からのポリエステル等)、シリコーンポリ
オール、ヒマシ油等が用いられ、市販品ではEC261
OA (ポリウレタン化成社)、LIRICH−30(
伊藤製油社)が例示される。Examples of polyols include low molecular weight polyols (ethylene glycol, diethylene glycol, dipropylene glycol, 114-butanediol, etc.), polyether polyols (polyethylene glycol, polyoxypropylene glycol, ethylene oxide-propylene oxide copolymer, etc.), and polyester polyols (polyethylene glycol, polyoxypropylene glycol, ethylene oxide-propylene oxide copolymer, etc.). β-methyl-δ-)hererolactone, polycaprolactone, polyester from diol dibasic acid, etc.), silicone polyol, castor oil, etc. are used, and commercially available products have an EC261
OA (Polyurethane Kasei Co., Ltd.), LIRICH-30 (
Ito Oil Co., Ltd.) is an example.
水和金属酸化物としては、高温度において脱水反応によ
る難燃化作用を示す薬剤が用いられ、たとえば水酸化マ
グネシウム、水酸化アルミニウム等が例示される。水和
金属酸化物は平均粒径が0.05〜50μm、特に10
μm以下の微粒子のものが好ましい。なお水和金属酸化
物は、表面処理したものであってもなくてもよいが、一
般に表面処理したものは本発明材への分散性、耐火性等
の特性に好結果を与えるので好ましい。特に好ましい水
和金属酸化物は、飽和脂肪酸、不飽和脂肪酸、シランカ
ップリング剤、チタンカップリング剤、シリコンオリゴ
マーで表面処理された水酸化マグネシウムである。As the hydrated metal oxide, an agent that exhibits a flame retardant effect through a dehydration reaction at high temperatures is used, such as magnesium hydroxide, aluminum hydroxide, and the like. The hydrated metal oxide has an average particle size of 0.05 to 50 μm, especially 10 μm.
Fine particles of micrometers or less are preferred. The hydrated metal oxide may or may not be surface-treated, but surface-treated ones are generally preferable because they give good results in properties such as dispersibility in the material of the present invention and fire resistance. Particularly preferred hydrated metal oxides are magnesium hydroxide surface-treated with saturated fatty acids, unsaturated fatty acids, silane coupling agents, titanium coupling agents, and silicon oligomers.
本発明においては、上記成分の他に通常の難燃剤、着色
剤、加工助剤、酸化防止剤、接着賦与剤等を配合しても
よい。特に通常の難燃剤や接着賦与剤を配合して、それ
ぞれ難燃性や接着性を改善することは好ましい。In the present invention, ordinary flame retardants, colorants, processing aids, antioxidants, adhesive agents, etc. may be added in addition to the above-mentioned components. In particular, it is preferable to incorporate common flame retardants and adhesive agents to improve flame retardancy and adhesive properties, respectively.
通常の難燃剤としては、三酸化アンチモン、ホウ酸亜鉛
、赤リン、ホウケイ酸鉛等の無機難燃剤、デカブロモジ
フェニルオキサイド、トリブロムフェノール、テトラブ
ロムビスフェノールA、テトラブロムキルン、臭素化ポ
リオール、ジブロモネオペンチルグリコール、パークロ
ロペンタシクロデカン、塩素化パラフィン等のハロゲン
系有機難燃剤、リン酸エステル、縮合リン酸アンモニウ
ム、リン酸メラミン、ポリリン酸カルバメート、脂肪族
ホスホン酸エステル等の有機リン系難燃剤等が例示され
る。Common flame retardants include inorganic flame retardants such as antimony trioxide, zinc borate, red phosphorous, lead borosilicate, decabromodiphenyl oxide, tribromophenol, tetrabromobisphenol A, tetrabromokiln, brominated polyols, and dibromodiphenyloxide. Halogen-based organic flame retardants such as neopentyl glycol, perchloropentacyclodecane, and chlorinated paraffin; organic phosphorus-based flame retardants such as phosphoric acid esters, condensed ammonium phosphates, melamine phosphates, polyphosphoric acid carbamates, and aliphatic phosphonic acid esters. etc. are exemplified.
接着賦与剤としては、タッキファイヤ等の粘着剤、ンラ
ン化合物、チタンカップリング剤、反応性シリコンオリ
ゴマー等が例示される。Examples of adhesive agents include adhesives such as tackifiers, Nran compounds, titanium coupling agents, and reactive silicone oligomers.
各成分の使用量については、液状ポリウレタンは、液状
ポリクロロプレン100重量部あたり50〜500重量
部、特に100〜250重量部である。50重量部より
少ないと所望個所への施与後における大気中での自己硬
化性が悪く、一方500重量部より多いと難燃性が低下
する。Regarding the amount of each component used, the amount of liquid polyurethane used is 50 to 500 parts by weight, particularly 100 to 250 parts by weight, per 100 parts by weight of liquid polychloroprene. If it is less than 50 parts by weight, self-curing properties in the atmosphere after application to a desired location will be poor, while if it is more than 500 parts by weight, flame retardancy will be reduced.
水和金属酸化物は、液状ポリクロロプレン100重量部
あたり50〜500重量部、特に100〜400重量部
である。50重量部より少ないと難燃性が乏しく、一方
500重量部より多いと伸び特性及び接着性が低下する
。The amount of hydrated metal oxide is from 50 to 500 parts by weight, in particular from 100 to 400 parts by weight, per 100 parts by weight of liquid polychloroprene. If it is less than 50 parts by weight, flame retardancy will be poor, while if it is more than 500 parts by weight, elongation properties and adhesive properties will be reduced.
上記したような通常の難燃剤を併用する場合、過大量使
用すると本発明のシール材の物性を低下させるので、そ
の使用量は液状ポリクロロプレン100重量部あたり1
00重量部以下、特に5〜70重置部とすることが好ま
しい。その範囲であれば、本発明シール材の耐候性並び
に接着性に悪影響を及ぼすことなく難燃性や耐火性を一
層改善する効果がある。When using a common flame retardant as described above, the physical properties of the sealing material of the present invention will be deteriorated if an excessive amount is used, so the amount used is 1 per 100 parts by weight of liquid polychloroprene.
00 parts by weight or less, particularly preferably 5 to 70 parts by weight. Within this range, the flame retardance and fire resistance of the sealing material of the present invention can be further improved without adversely affecting the weather resistance and adhesiveness.
本発明のシール材は、前記した通り、種々の優れた性能
を有ししかも安価であるので、各種分野での就中建築用
のシーリング材として頗る有用である。As described above, the sealing material of the present invention has various excellent performances and is inexpensive, so it is extremely useful as a sealing material for various fields, especially for construction.
以下、実施例並びに比較例によって本発明を一層詳細に
説明すると同時に本発明の優れた効果を示す。以下にお
ける数値は、すべて重量部あるいは重量%である。EXAMPLES Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples, and at the same time, the excellent effects of the present invention will be shown. All numerical values below are parts by weight or weight %.
実施例1〜8、比較例1〜3
第1表に示すの各成分を同表に示す量比で三本ロールを
用いて充分混合し、実施例1〜8及び比較例1〜3のシ
ール材を得た。Examples 1 to 8, Comparative Examples 1 to 3 Each component shown in Table 1 was thoroughly mixed in the amount ratio shown in the same table using a triple roll, and the seals of Examples 1 to 8 and Comparative Examples 1 to 3 were prepared. I got the material.
次いで以下に示す方法によりそれぞれのシール材の特性
を評価した。それらの結果を同表に一緒に示す。Next, the characteristics of each sealing material were evaluated by the method shown below. The results are shown together in the same table.
自己硬化性:
三本ロールを用いて充分混合して得た直後のシール材を
1m+w厚さのシート状に成形して室温下で24時間大
気中に放置し、その後における硬化度を調べる。ヘタツ
キの有るものを×、ヘタツキの無いものを○とする。Self-curing property: Immediately after thorough mixing using a triple roll, the sealing material obtained is formed into a sheet with a thickness of 1 m+w and left in the air at room temperature for 24 hours, and the degree of curing is then examined. If there is some damage, mark it as ×, and if there is no damage, mark it as ○.
機械特性:
上記した自己硬化性試験において得られた大気中24時
間放置後のシートからJIS K6301に規定の3号
ダンヘルを打ち抜き、それにつき引っ張り試験を行う。Mechanical properties: A No. 3 Dangel specified in JIS K6301 is punched out from the sheet obtained in the above self-curing test after being left in the atmosphere for 24 hours, and a tensile test is performed on it.
伸びが100%未満のものを×、100%以」二のもの
を○とする。If the elongation is less than 100%, it is marked as ×, and if it is more than 100%, it is marked as ○.
難燃性:
JIS K7201に規定する方法に従って酸素指数を
測定する。Flame retardancy: Oxygen index is measured according to the method specified in JIS K7201.
耐火性:
約1000℃のバーナーにて厚さ3龍、長さ50n、幅
6龍の寸法、形状の試料を5分かけて燃焼し、灰化する
。試料が燃焼前の形状、又はそれに近い形状を保持した
ままで灰化するものを○、燃焼によって大きく形崩れす
るものを×とする。Fire resistance: A sample with dimensions and shape of 3 mm thick, 50 nm long, and 6 mm wide is burned and incinerated in a burner at approximately 1000°C for 5 minutes. A sample that ashes while retaining its pre-combustion shape or a shape close to it is rated as ○, and a sample that loses its shape significantly due to combustion is marked as ×.
耐候性
各々の組成物を室温で24時間放置して硬化した後、サ
ンシャインウェザメータで2000時間曝露した。カビ
による黒汚染の認められたものを×、カビの発生がない
ものを○とする。Weather Resistance Each composition was left to stand at room temperature for 24 hours to cure, and then exposed using a sunshine weather meter for 2000 hours. Those with black contamination due to mold are marked as ×, and those with no mold growth are marked as ○.
接着性:
予めモルタルブロック上にウレタン系プライマーで処理
を行った後、各組成物を厚さ2fl、輻10m1にコー
トし、室ムで24時間放置後モルタルと各組成物間の剥
離の有無で評価し、シール材が未硬化で伸びるもの、シ
ートが脆くて容易に剥離するものを×、容易に剥離しな
いものを○とする。Adhesion: After pre-treating the mortar block with a urethane primer, each composition was coated to a thickness of 2 fl and a width of 10 m1, and after being left in a room for 24 hours, the presence or absence of peeling between the mortar and each composition was determined. The sealing material was evaluated as uncured and stretched, the sheet was brittle and peeled off easily, and the sheet was evaluated as ×, and the sheet that was not easily peeled off as ○.
〔以丁余白][Icho margin]
Claims (2)
プレン100重量部あたり50〜500重量部の液状ポ
リウレタン、50〜500重量部の水和金属酸化物とか
らなることを特徴とする難燃性シーリング材。(1) A flame-retardant sealing material comprising liquid polychloroprene, 50 to 500 parts by weight of liquid polyurethane, and 50 to 500 parts by weight of a hydrated metal oxide per 100 parts by weight of the liquid polychloroprene.
100重量部の通常難燃剤をさらに有することを特徴と
する第1請求項に記載の難燃性シーリング材。(2) 5 to 100 parts by weight of liquid polychloroprene
A flame-retardant sealant according to claim 1, further comprising 100 parts by weight of a conventional flame retardant.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP945590A JPH03212477A (en) | 1990-01-17 | 1990-01-17 | Flame-retardant sealing material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP945590A JPH03212477A (en) | 1990-01-17 | 1990-01-17 | Flame-retardant sealing material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH03212477A true JPH03212477A (en) | 1991-09-18 |
Family
ID=11720768
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP945590A Pending JPH03212477A (en) | 1990-01-17 | 1990-01-17 | Flame-retardant sealing material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03212477A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006257118A (en) * | 2005-03-15 | 2006-09-28 | Denki Kagaku Kogyo Kk | Sponge shaped body |
-
1990
- 1990-01-17 JP JP945590A patent/JPH03212477A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006257118A (en) * | 2005-03-15 | 2006-09-28 | Denki Kagaku Kogyo Kk | Sponge shaped body |
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