JPH0269559A - Reduction of tackiness of urethane elastomer - Google Patents
Reduction of tackiness of urethane elastomerInfo
- Publication number
- JPH0269559A JPH0269559A JP22202388A JP22202388A JPH0269559A JP H0269559 A JPH0269559 A JP H0269559A JP 22202388 A JP22202388 A JP 22202388A JP 22202388 A JP22202388 A JP 22202388A JP H0269559 A JPH0269559 A JP H0269559A
- Authority
- JP
- Japan
- Prior art keywords
- urethane
- drying oil
- oil
- tackiness
- curing agent
- 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
- 229920006311 Urethane elastomer Polymers 0.000 title claims abstract description 15
- 238000001035 drying Methods 0.000 claims abstract description 16
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 9
- 239000003054 catalyst Substances 0.000 claims abstract description 8
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 6
- 239000000945 filler Substances 0.000 claims abstract description 6
- 239000004014 plasticizer Substances 0.000 claims abstract description 6
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000003921 oil Substances 0.000 abstract description 16
- 235000019198 oils Nutrition 0.000 abstract description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 6
- 235000021388 linseed oil Nutrition 0.000 abstract description 2
- 239000000944 linseed oil Substances 0.000 abstract description 2
- 239000002383 tung oil Substances 0.000 abstract description 2
- 238000013329 compounding Methods 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 238000010276 construction Methods 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000000806 elastomer Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 229920005862 polyol Polymers 0.000 description 5
- 150000003077 polyols Chemical class 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000004721 Polyphenylene oxide Chemical group 0.000 description 3
- 229920000570 polyether Chemical group 0.000 description 3
- 238000004078 waterproofing Methods 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003566 sealing material Substances 0.000 description 2
- WLNBMPZUVDTASE-HXIISURNSA-N (2r,3r,4s,5r)-2-amino-3,4,5,6-tetrahydroxyhexanal;sulfuric acid Chemical compound [O-]S([O-])(=O)=O.O=C[C@H]([NH3+])[C@@H](O)[C@H](O)[C@H](O)CO.O=C[C@H]([NH3+])[C@@H](O)[C@H](O)[C@H](O)CO WLNBMPZUVDTASE-HXIISURNSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000003254 anti-foaming effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- ZFTFAPZRGNKQPU-UHFFFAOYSA-N dicarbonic acid Chemical compound OC(=O)OC(O)=O ZFTFAPZRGNKQPU-UHFFFAOYSA-N 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052806 inorganic carbonate Inorganic materials 0.000 description 1
- 229910021331 inorganic silicon compound Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
本発明は、土木建築用に用いられる常温硬化型ウレタン
エラストマーの改良、さらに詳しくは、シーリング材、
防水材などとして利用される常温硬化型ウレタンエラス
トマーにおいて、施工後の表面粘若性を解消させる方法
に関する。
(背景)
現在土木建築分野においてシーリング材、防水材などと
して広く用いられている常温硬化型ウレタンエラストマ
ーは、例えば末端イソシアネート基を有するウレタンプ
レポリマーとポリエーテルポリオール及び3,3°−ジ
クロル−4,4゛−ジアミノジフェニルメタン等の活性
水素を有する化合物に、可塑剤、触媒、消泡剤、充填剤
等を配合した硬化剤を所定の比率で混合した組成物を旅
工部位の注入又は塗布することにより形成される。得ら
れたウレタンプレポリマーは、ゴム弾性、耐候性、耐薬
品性、耐水性等に優れているので、建物の屋上や壁面な
どのシーリング材、防水材として広く用いられている。
(従来技術の問題点)
しかしながら、このような従来のウレタンプレポリマー
では、施工後のポリマー層表面に長く粘着性が残存し、
このため、該表面が施工後に埃等により汚染され易い点
が問題となっていた。
そこで対策として。
(1)オクチル耐鉛、ジブチル錫ジラウレート等の金属
触媒の使用量を増大したり又はオクチル酸、フタル酸等
の酸触媒を併用する方法。
(2)ウレタンプレポリマーや硬化剤中のポリエーテル
ポリオールの官能基数を通常より大きくする方法。
などが行なわれている。
しかしながら、これら従来の表面粘着性低下法において
、(1)では調合後の可使時間が短くなるため施工が困
難になると共に、仕上りが悪くなり、また(2)では、
生成エラストマー層の物性、特に伸びが低下し、クラッ
クに対する追従性に欠けるなどの欠点を生じる。The present invention aims to improve room temperature curing urethane elastomers used for civil engineering and construction, and more specifically, to improve sealing materials,
This invention relates to a method for eliminating surface viscosity after construction in room-temperature curing urethane elastomers used as waterproofing materials. (Background) Room-temperature curable urethane elastomers, which are currently widely used as sealants, waterproofing materials, etc. in the civil engineering and construction fields, include, for example, urethane prepolymers with terminal isocyanate groups, polyether polyols, 3,3°-dichloro-4, Injecting or applying a composition prepared by mixing a compound having active hydrogen such as 4-diaminodiphenylmethane with a hardening agent containing a plasticizer, a catalyst, an antifoaming agent, a filler, etc. in a predetermined ratio to the work site. formed by. The obtained urethane prepolymer has excellent rubber elasticity, weather resistance, chemical resistance, water resistance, etc., and is therefore widely used as a sealing material and waterproofing material for the roofs and walls of buildings. (Problems with conventional technology) However, with such conventional urethane prepolymers, stickiness remains on the surface of the polymer layer for a long time after application.
For this reason, there has been a problem in that the surface is easily contaminated by dust and the like after construction. So as a countermeasure. (1) A method of increasing the amount of a metal catalyst such as octyl lead-resistant or dibutyltin dilaurate, or using an acid catalyst such as octylic acid or phthalic acid in combination. (2) A method in which the number of functional groups in the polyether polyol in the urethane prepolymer or curing agent is made larger than usual. etc. are being carried out. However, in these conventional methods for reducing surface tackiness, (1) shortens the pot life after preparation, making it difficult to apply and resulting in a poor finish, and (2),
The physical properties of the resulting elastomer layer, especially its elongation, deteriorate, resulting in drawbacks such as a lack of crack followability.
よって本発明が解決しようとする課題は、調合物の可使
時間や生成エラストマーの物性に影響を与えることなし
に、施工後のウレタンエラストマーの粘着性を低下させ
るための方法乃至表面貼Zi性ノ乏しいウレタンエラス
トマーを提供することである。Therefore, the problem to be solved by the present invention is to develop a method for reducing the adhesiveness of urethane elastomer after application without affecting the pot life of the preparation or the physical properties of the produced elastomer, The object of the present invention is to provide a poor urethane elastomer.
(Jl要)
本発明は、上記課題を解決せんがため、末端イソシアネ
ート基を有するウレタンプレポリマー(A)と、活性水
素を有する化合物及び必要に応じ可塑剤、触媒、消泡剤
、充填剤等を配合した硬化剤CB)を混合し反応、硬化
させるに当たり、前記(A)及び(B)の混合物に対し
、乾性油を0.1〜5ffL量%の割で添加することを
特徴とするウレタンエラストマーの粘着性低下法を要旨
とする。以下1発明に関連する諸事項につき項分けして
説明する・
(乾性油)
本発明に使用する乾性油としては、アマニ油、桐油、エ
ノ油等の沃素価130以上の植物油脂等が挙げられ、こ
れらは単独又は二種以上を組み合わせたものも使用でき
る。
以上の乾性油は、使用直前にプレポリマー及び硬化剤の
双方又は一方に或は両者の調合物中に添加することもで
きるが、使用上の便宜を考慮して、予めプレポリマー及
び/又は硬化剤中に乾性油を混合しておくのが好ましい
、但し本発明は、あながち上述の二液型のものに限らず
、−液型のものにも利用可能であるから、この場合、乾
性油は当然組成物に直接配合される。
乾性油の添加量は、末端イソシアネート基を有するウレ
タンプレポリマー(A)と、活性水素を有する化合物及
び必要に応じ可塑剤、触媒、消泡剤、充填剤等を配合し
た硬化剤(B)との合計量に対し、0.1重量%以上、
5!f!量%以下の範囲内であるのが好ましい、添加量
が0.1ffi量%未満では粘着性改良の効果が乏しく
、また5重量%超過では、生成したウレタンエラストマ
ー表面に乾性油の厚い皮膜が生じるので好ましくない。
(その他の成分)
本発明で使用する末端イソシアネートを有するウレタン
プレポリマーは、ポリエーテルポリオール等のヒドロキ
シ化合物にトリレンジイソシアネート、ジフェニルメタ
ン−4,4゛−ジイソシアネート、ヘキサメチレンイソ
シアネートなどのイソシアネート類の過剰量を反応させ
たものである。
また、硬化剤成分である活性水素を有する化合物として
は、エチレングリコール、ブタンジオールなどの低分子
量ポリオール類、ポリオキシプロピレングリコールなど
のポリオキシアルキレングリコール類、3.3°−ジク
ロル−4,4°−ジアミノジフェニルメタンなどのポリ
アミン類が挙げられる。
以上の主成分以外に、必要に応じ配合できる副成分とし
て下記のような物質又は材料を例示することができるが
、勿論例示のものだけに限る訳ではない。
可塑剤ニジオクチルフタレート、ジオクチルアジペート
、塩素化パラフィン等。
触媒:オクチル酸鉛、ジブチル錫ジラウレート等。
消泡剤ニジメチルポリシロキサンなどのシリコーン油、
ポリブテンなどのオレフィン系炭化水素等。
充填剤二炭酪カルシウムなどの無機炭酸塩類、シリカな
どの無機ケイ素化合物、酸化チタンなどの金居耐化物。
その他:顔料、紫外線吸収剤、泡化防止剤等。
因に1以上の物質又は材料は、土木建築用途に用いられ
る常温硬化型ウレタンエラストマーに添加される物質又
は材料として既知のものである。(Required Jl) In order to solve the above problems, the present invention comprises a urethane prepolymer (A) having terminal isocyanate groups, a compound having active hydrogen, and if necessary, a plasticizer, a catalyst, an antifoaming agent, a filler, etc. A urethane characterized by adding a drying oil in an amount of 0.1 to 5 ffL% to the mixture of (A) and (B) when mixing, reacting and curing the curing agent CB) containing the above. The gist is a method for reducing the tackiness of elastomers. Below, various matters related to the invention will be explained in terms of section. (Drying oil) Examples of the drying oil used in the present invention include vegetable oils and fats with an iodine value of 130 or more, such as linseed oil, tung oil, and eno oil. , these can be used alone or in combination of two or more. The above-mentioned drying oil can be added to the prepolymer and/or curing agent, or to a formulation of both, immediately before use. It is preferable to mix a drying oil into the agent; however, the present invention is not limited to the above-mentioned two-liquid type, but can also be used for a -liquid type, so in this case, the drying oil is Naturally, it is directly incorporated into the composition. The amount of drying oil added is determined by combining a urethane prepolymer (A) with terminal isocyanate groups, a curing agent (B) containing a compound having active hydrogen, and optionally a plasticizer, a catalyst, an antifoaming agent, a filler, etc. 0.1% by weight or more based on the total amount of
5! f! The amount added is preferably within the range of 0.1% by weight or less, the effect of improving adhesion is poor, and if it exceeds 5% by weight, a thick film of drying oil will form on the surface of the produced urethane elastomer. So I don't like it. (Other components) The urethane prepolymer having a terminal isocyanate used in the present invention contains an excess amount of isocyanates such as tolylene diisocyanate, diphenylmethane-4,4'-diisocyanate, and hexamethylene isocyanate in addition to a hydroxy compound such as polyether polyol. It is a reaction of Compounds having active hydrogen that are curing agent components include low molecular weight polyols such as ethylene glycol and butanediol, polyoxyalkylene glycols such as polyoxypropylene glycol, and 3.3°-dichloro-4,4° -Polyamines such as diaminodiphenylmethane can be mentioned. In addition to the above-mentioned main components, the following substances or materials can be exemplified as subcomponents that can be added as necessary, but of course they are not limited to only the exemplified ones. Plasticizers nidioctyl phthalate, dioctyl adipate, chlorinated paraffin, etc. Catalyst: lead octylate, dibutyltin dilaurate, etc. antifoaming silicone oil such as dimethylpolysiloxane;
Olefinic hydrocarbons such as polybutene. Fillers: Inorganic carbonates such as dicarbonate butycalcium, inorganic silicon compounds such as silica, and metal-resistant materials such as titanium oxide. Others: pigments, ultraviolet absorbers, anti-foaming agents, etc. In particular, one or more substances or materials are known as substances or materials added to cold-curing urethane elastomers used in civil engineering and construction applications.
本発明に従い乾性油を含むウレタンエラストマーが施工
部位に形成されると、空気中の酸素によりリノキシン化
した乾性油からなる極めて薄い皮膜が未硬化状態に在る
該エラストマー層の表面を覆う結果、該表面の粘着性が
消失し又は低下するものと推定される。従って、不飽和
度の高い乾性油程、粘着性解消効果が高い、なお、乾性
油のリノキシン化した皮膜は、優れた耐候性を有するか
ら、全体としての耐候性も一層向上する。When a urethane elastomer containing a drying oil is formed at a construction site according to the present invention, an extremely thin film of the drying oil that has been linoxinized by oxygen in the air covers the surface of the uncured elastomer layer. It is estimated that the surface tackiness disappears or decreases. Therefore, the higher the degree of unsaturation of the drying oil, the higher the tack-resolving effect.In addition, since the linoxinized film of the drying oil has excellent weather resistance, the weather resistance as a whole is further improved.
以下、実施例及び比較例により発明実施の形態及び効果
を示すが、例示は当然説明用のもので発明の技術的範囲
を制限し又は限定するためのものではない。
実施例
下表−1に示す配合で、 JIS A 602+に準じ
てウレタンエラストマー試験片を作成し、if価を行っ
た。但し、硬化剤は、予め(イハラキュアミン%7))
2)を(ポリバードナT500))3)に溶解した後で
、これに他の原料を加え、混合、分散させた。
なお、以下の配合は31部で示される。
(以下余白)
表−1
注1)出願人会社製ウレタンプレポリマーの商品名(N
GO)含有i3.7$; 2)イハラケミカル工業■製
の3,3゛−ジクロル−4,4°−ジアミノジフェニル
メタンの商品名;3)出願人会社製ポリオールの商品名
(水酸基価35) ; 4日本化学産業昧製の硬化触
媒の商品名、 5)JIS A 602+に準する無処
理、 20”Cの測定値、[1)20℃、3日後のウレ
タンエラストマーの表面を触診して判定。
上表から明らかな通り、本発明により乾性油を添加され
た試料は、無添加の対象と比較して、ベタツキが全くな
いのみでなく、物性的にも良好な成績を示している。Hereinafter, the embodiments and effects of the invention will be illustrated by Examples and Comparative Examples, but the examples are, of course, for illustrative purposes and are not intended to limit or limit the technical scope of the invention. Examples Urethane elastomer test pieces were prepared according to JIS A 602+ using the formulations shown in Table 1 below, and the IF value was determined. However, the curing agent must be prepared in advance (Ihalacyuamine% 7))
After 2) was dissolved in (Polyvar Dona T500)) 3), other raw materials were added thereto and mixed and dispersed. In addition, the following formulation is shown in 31 parts. (Space below) Table 1 Note 1) Trade name of urethane prepolymer manufactured by the applicant company (N
GO) containing i3.7$; 2) Trade name of 3,3゛-dichloro-4,4°-diaminodiphenylmethane manufactured by Ihara Chemical Industry ■; 3) Trade name of polyol manufactured by applicant company (hydroxyl value 35); 4. Trade name of curing catalyst made by Nippon Kagaku Sangyo. 5) No treatment according to JIS A 602+, measured value at 20"C. [1) Determined by palpating the surface of the urethane elastomer after 3 days at 20°C. As is clear from the above table, the samples to which the drying oil was added according to the present invention not only had no stickiness at all, but also showed better physical properties than the samples to which no additive was added.
以上、説明した通り、本発明は、調合物の可使時間や生
成エラストマーの物性に影響を与えることなしに、施工
後のウレタンエラストマーの粘着性を低下させるための
方法乃至表面粘着性の乏しいウレタンエラストマーの提
供を可能ならしめたことにより、土木建築分野のみなら
ず、表面粘着性の望ましくない塗装分野等に対し顕著な
貢献を果しうる。
特許出願人 第一工業製薬株式会社As explained above, the present invention provides a method for reducing the tackiness of a urethane elastomer after application without affecting the pot life of the formulation or the physical properties of the produced elastomer, or a urethane elastomer with poor surface tackiness. By making it possible to provide an elastomer, it is possible to make a significant contribution not only to the field of civil engineering and construction, but also to the field of painting, where surface tackiness is undesirable. Patent applicant Daiichi Kogyo Seiyaku Co., Ltd.
Claims (1)
A)と、活性水素を有する化合物及び必要に応じ可塑剤
、触媒、消泡剤、充填剤等を配合した硬化剤(B)を混
合し反応、硬化させるに当たり、前記(A)及び(B)
の混合物に対し、乾性油を0.1〜5重量%の割で添加
することを特徴とするウレタンエラストマーの粘着性低
下法。Urethane prepolymer with terminal isocyanate groups (
When mixing A) and a curing agent (B) containing a compound having active hydrogen and, if necessary, a plasticizer, a catalyst, an antifoaming agent, a filler, etc., and reacting and curing the above (A) and (B).
A method for reducing the tackiness of a urethane elastomer, which comprises adding a drying oil in an amount of 0.1 to 5% by weight to the mixture.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22202388A JPH0269559A (en) | 1988-09-05 | 1988-09-05 | Reduction of tackiness of urethane elastomer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22202388A JPH0269559A (en) | 1988-09-05 | 1988-09-05 | Reduction of tackiness of urethane elastomer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0269559A true JPH0269559A (en) | 1990-03-08 |
Family
ID=16775889
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP22202388A Pending JPH0269559A (en) | 1988-09-05 | 1988-09-05 | Reduction of tackiness of urethane elastomer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0269559A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0477899A2 (en) * | 1990-09-26 | 1992-04-01 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Curable composition |
-
1988
- 1988-09-05 JP JP22202388A patent/JPH0269559A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0477899A2 (en) * | 1990-09-26 | 1992-04-01 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Curable composition |
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