JP3008284B1 - Modified silicone sealant for construction - Google Patents
Modified silicone sealant for constructionInfo
- Publication number
- JP3008284B1 JP3008284B1 JP3899599A JP3899599A JP3008284B1 JP 3008284 B1 JP3008284 B1 JP 3008284B1 JP 3899599 A JP3899599 A JP 3899599A JP 3899599 A JP3899599 A JP 3899599A JP 3008284 B1 JP3008284 B1 JP 3008284B1
- Authority
- JP
- Japan
- Prior art keywords
- modified silicone
- weight
- polymer
- air
- sealing material
- 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.)
- Expired - Fee Related
Links
- 238000010276 construction Methods 0.000 title claims description 5
- 239000004590 silicone sealant Substances 0.000 title claims 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 20
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 19
- 229920000642 polymer Polymers 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 7
- 239000004094 surface-active agent Substances 0.000 claims abstract description 7
- 229920001971 elastomer Polymers 0.000 claims abstract description 6
- 229920000620 organic polymer Polymers 0.000 claims abstract description 6
- 239000005060 rubber Substances 0.000 claims abstract description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 239000010703 silicon Substances 0.000 claims abstract description 4
- 239000004014 plasticizer Substances 0.000 claims description 15
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims description 3
- 239000003566 sealing material Substances 0.000 abstract description 14
- 229920002050 silicone resin Polymers 0.000 description 9
- -1 acryl Chemical group 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000000945 filler Substances 0.000 description 5
- 230000008602 contraction Effects 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 230000000740 bleeding effect Effects 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- 230000009974 thixotropic effect Effects 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229910018540 Si C Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000029052 metamorphosis Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000035515 penetration Effects 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
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
【要約】
【課題】建築用変成シリコーン系シーリング材におい
て、表面タックの少ない耐候性良好な組成物を提供する
ことを目的とする。
【解決手段】(A)珪素原子に結合した水酸基および
(または)加水分解性基を有し、シロキサン結合を形成
することにより架橋しうる珪素含有基を少なくとも1個
有するゴム系有機重合体、(B)シリコーン系界面活性
剤、(C)空気硬化性化合物、および(D)分子量1,
000以上のポリオキシアルキレン重合体を含有してな
る建築用変成シリコーン系シーリング材組成物を使用す
る。An object of the present invention is to provide a modified silicone sealing material for architectural use, which has a low surface tack and a good weather resistance. (A) A rubber-based organic polymer having at least one silicon-containing group that has a hydroxyl group and / or a hydrolyzable group bonded to a silicon atom and can be crosslinked by forming a siloxane bond, B) a silicone surfactant, (C) an air-curable compound, and (D) a molecular weight of 1,
Use is made of a modified silicone sealing material composition for buildings containing at least 000 polyoxyalkylene polymer.
Description
【0001】[0001]
【発明の属する技術】本発明は、建築物の内外装の部材
間やジョイント部の目地に充填し、風雨の侵入を防止す
る建築用変成シリコーン系シーリング材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a modified silicone-based sealing material for buildings, which is filled between joints at the interior and exterior of buildings and joints at joints to prevent the penetration of wind and rain.
【0002】更に詳しくは,JIS A 5758に規
定されている建築用シーリング材系統に属し、表面タッ
ク、耐候性の良好な変成シリコーン系シーリング材に関
する。More specifically, the present invention relates to a modified silicone-based sealing material which belongs to a family of building sealing materials specified in JIS A 5758 and has good surface tack and weather resistance.
【0003】[0003]
【従来の技術】建築用変成シリコーン系シーリング材
は、ペースト状に調整された一成分または、二成分で提
供され、これを建築物の目地に充填・施工し硬化させ
る。このシーリング材は、主成分としてシロキサン結合
を形成することにより架橋しうる珪素含有基を有するゴ
ム系有機重合体(以下変成シリコーン樹脂という)、硬
化剤、硬化促進剤、硬化遅延剤、可塑剤、充填剤、酸化
防止剤、紫外線防止剤、染・顔料等からなる組成物であ
り、経済性に優れ、かつ耐候性等の特性が、ポリウレタ
ン、ポリサルファイドなどの他の系より、総合的に優れ
るため近年ますます多用されている。2. Description of the Related Art A modified silicone sealing material for construction is provided as one or two components prepared in the form of a paste, which is filled into a joint of a building, applied and cured. The sealing material is a rubber-based organic polymer having a silicon-containing group capable of crosslinking by forming a siloxane bond as a main component (hereinafter, referred to as a modified silicone resin), a curing agent, a curing accelerator, a curing retarder, a plasticizer, A composition consisting of fillers, antioxidants, UV inhibitors, dyes / pigments, etc., because it is economical and has properties such as weather resistance that are generally better than other systems such as polyurethane and polysulfide. In recent years, it has been increasingly used.
【0004】しかし、変成シリコーン系シーリング材
は、硬化物表面のタックが多く、長期の屋外暴露におい
て汚れ易い欠点がある。[0004] However, the modified silicone-based sealing material has a disadvantage that the surface of the cured product has a large amount of tack and is easily stained during long-term outdoor exposure.
【0005】このタック軽減のため、乾性油に代表され
る空気硬化性化合物を添加することが行われている(特
公平5−82860)。これは、空気硬化性化合物の1
部が表面にブリードし硬化する機構によるものである。[0005] In order to reduce the tack, an air-curable compound represented by a drying oil is added (Japanese Patent Publication No. 5-82860). This is one of the air-curable compounds
This is due to a mechanism in which the part bleeds and hardens on the surface.
【0006】[0006]
【発明が解決しようとする課題】しかしながら、この空
気硬化性化合物を添加した場合、ブリードがさらに進行
して、長期において硬化物表面が内部に比べ、高硬度、
低伸びとなる。そのため、目地伸縮により表面クラック
が発生し外観不良となる場合がある。また、目地構造
上、施工上の問題で発生する薄層の部分においては、硬
化劣化が著しいという欠点がある。However, when this air-curable compound is added, the bleeding proceeds further, and the surface of the cured product has a higher hardness than the interior over a long period of time.
Low elongation. For this reason, surface cracks may occur due to joint expansion and contraction, resulting in poor appearance. Further, there is a disadvantage that the hardening deterioration is remarkable in a thin layer portion generated due to a joint structure and a problem in construction.
【0007】特に、変成シリコーン樹脂として、高分子
量、かつ単分散のものを用いた場合、均一な架橋構造が
得られ、硬化性、硬化物のゴム物性は良好なシーリング
材を容易に調整することが可能だが、空気硬化性化合物
を添加すると上記現象が顕著になることが判った。In particular, when a modified silicone resin of high molecular weight and monodisperse is used, a uniform crosslinked structure can be obtained, and the curability and the rubber properties of the cured product can be easily adjusted with a good sealing material. However, it was found that the above phenomenon became remarkable when an air-curable compound was added.
【0008】上記欠点があるため、空気硬化性化合物
は、配合量を少なく制限せざるをえず、そのため、当初
の目的であるタック防止の効果が十分に得られない。Due to the above-mentioned disadvantages, the amount of the air-curable compound must be limited to a small amount, and therefore, the effect of preventing tackiness, which is the original object, cannot be sufficiently obtained.
【0009】一方、配合成分中の可塑剤は、混合物のチ
キソトロピック性、粘性等を調節し、例えば、混合性、
ガン打ち性、へら仕上げ性等の充填作業性、スランプ
性、混合物の柔軟性を得るために必須の成分である。On the other hand, the plasticizer in the compounding component adjusts the thixotropic property, viscosity and the like of the mixture.
It is an essential component to obtain filling workability such as gunning property and spatula finish, slump property, and flexibility of the mixture.
【0010】この可塑剤としては、フタル酸エステル系
の低分子量可塑剤が一般に使用されるが、これら低分子
量可塑剤を使用した場合、充填剤の選択により所定の作
業性を容易に得ることが可能だが、ブリードによる物性
低下、すなわち表面にタックが出て、長期において可塑
剤の揮散によるモジュラス上昇、伸びの低下等が発生す
る。特に、高温下で施工した場合には物性低下が促進さ
れる。そのため、空気硬化性化合物との組合せでは、初
期は空気硬化性化合物の効果が少ない一方、長期屋外曝
露された後では、表面硬度上昇を助長する傾向にある。As the plasticizer, phthalate low molecular weight plasticizers are generally used. When these low molecular weight plasticizers are used, a predetermined workability can be easily obtained by selecting a filler. Although it is possible, physical properties are reduced due to bleeding, that is, tack is generated on the surface, and an increase in modulus and a decrease in elongation due to volatilization of the plasticizer occur in a long term. In particular, when construction is performed at a high temperature, deterioration of physical properties is promoted. Therefore, in combination with an air-curable compound, the effect of the air-curable compound is initially small, but after long-term outdoor exposure, it tends to promote an increase in surface hardness.
【0011】一方、ポリエステル、ポリエーテル、ポリ
−α−メチルスチレン、ポリブタジエン、ブタジエン−
アクリロニトリル共重合体、ポリクロロプレン、ポリイ
ソプレン、ポリブテン、塩素化パラフィン等の一般の高
分子可塑剤も提案されているが、低分子可塑剤に比べて
可塑化効率は悪くなるが、物性変化は少ない。しかしな
がら、シーリング材として、各種配合成分と混合してペ
ースト状にした組成物においては、低分子量可塑剤に比
べると、広範な相溶性が得られない。特に、無機充填材
のごとき、固体材料の湿潤、分散性が劣る欠点がある。
そのため、タック防止のために空気硬化性化合物を使用
する場合、相溶性が悪いため、表面硬度上昇が、初期よ
り発生しやすい欠点がある。On the other hand, polyester, polyether, poly-α-methylstyrene, polybutadiene, butadiene-
General polymer plasticizers such as acrylonitrile copolymer, polychloroprene, polyisoprene, polybutene, and chlorinated paraffin have also been proposed, but plasticization efficiency is lower than that of low-molecular plasticizers, but there is little change in physical properties. . However, a composition that is mixed with various components to form a paste as a sealing material cannot obtain a wide range of compatibility as compared with a low-molecular-weight plasticizer. In particular, there is a disadvantage that the wettability and dispersibility of a solid material are poor, such as an inorganic filler.
Therefore, when an air-curable compound is used to prevent tack, there is a disadvantage that the surface hardness is easily increased from the beginning because of poor compatibility.
【0012】本発明は、上記現状の変成シリコーン系シ
ーリング材の欠点を鑑みなされたもので、変成シリコー
ン樹脂に空気硬化性化合物を添加したした系において、
特定のシリコーン化合物と高分子可塑剤として分子量
1,000以上のポリオキシアルキレン重合体を併用す
ることによって、系内の相溶性が向上し、経時後の硬化
物表面硬度の過剰な上昇が緩和されることを見出した。The present invention has been made in view of the above-mentioned drawbacks of the present modified silicone-based sealing material, and has been developed in a system in which an air-curable compound is added to a modified silicone resin.
By using a specific silicone compound and a polyoxyalkylene polymer having a molecular weight of 1,000 or more as a polymer plasticizer, compatibility in the system is improved, and an excessive increase in surface hardness of a cured product after aging is moderated. I found that.
【0013】[0013]
【課題を解決するための手段】すなわち本発明は、
(A)珪素原子に結合した水酸基および(または)加水
分解性基を有し、シロキサン結合を形成することにより
架橋しうる珪素含有基を少なくとも1個有するゴム系有
機重合体100重量部に対し、(B)メチルポリシロキ
サン、ポリアルキレンオキサイドから構成されるシリコ
ーン系界面活性剤0.01〜5重量部、(C)空気硬化
性化合物1〜20重量部、(D)高分子可塑剤として分
子量1,000以上のポリオキシアルキレン重合体を含
有してなる建築用変成シリコーン系シーリング材組成物
に関するものである。That is, the present invention provides:
(A) 100 parts by weight of a rubber-based organic polymer having at least one silicon-containing group which has a hydroxyl group and / or a hydrolyzable group bonded to a silicon atom and can be crosslinked by forming a siloxane bond, (B) 0.01 to 5 parts by weight of a silicone surfactant composed of methylpolysiloxane and polyalkylene oxide, (C) 1 to 20 parts by weight of an air-curable compound, and (D) a molecular weight of 1 as a polymer plasticizer The present invention relates to a modified silicone-based sealing material composition for buildings, comprising 2,000 or more polyoxyalkylene polymers.
【0014】[0014]
【発明の実施の形態】(A)のゴム系有機重合体の例と
しては、例えば主鎖が実質的にポリエーテルやアクリル
などの重合体に反応性シリコーン官能基を導入した重合
体があげられる。数平均分子量としては、3,000〜
30,000が好ましいがより好ましくは15,000
〜20,000のもので、一般に変成シリコーン樹脂と
呼ばれるものである。これらの具体例としては、既に工
業的に生産されていて、「エクセスター」(旭硝子
(株)製)を利用できる。BEST MODE FOR CARRYING OUT THE INVENTION Examples of the rubber-based organic polymer (A) include, for example, a polymer whose main chain is substantially a polymer such as polyether or acryl, into which a reactive silicone functional group is introduced. . The number average molecular weight is from 3,000 to
30,000 is preferred, but 15,000 is more preferred.
~ 20,000, which is generally called a modified silicone resin. As an example of these, "Exester" (produced by Asahi Glass Co., Ltd.), which is already industrially produced, can be used.
【0015】(B)のシリコーン系界面活性剤とは、主
鎖として、主にジメチルシロキサンからなり、疎水基が
メチルシロキサン、親水基がポリアルキレンオキサイド
で構成される非イオン系の界面活性剤で、ジメチルシロ
キサン主鎖に対し、Si−C結合による側鎖変成コポリ
マー、もしくはSi−O−C結合の末端変成ポリマーと
して供給される。これは、Si濃度、ジメチルシロキサ
ン鎖長、アルキレンオキサイド種などの調節により、様
々な種類が工業的に生産されており、空気硬化性化合物
の種類、マトリクスの系の違いにより、任意のものを選
択できる。The silicone surfactant (B) is a nonionic surfactant mainly composed of dimethylsiloxane as a main chain, wherein the hydrophobic group is composed of methylsiloxane and the hydrophilic group is composed of polyalkylene oxide. The dimethylsiloxane main chain is supplied as a side chain modified copolymer with a Si—C bond or a terminal modified polymer with a Si—O—C bond. This is because various types are industrially produced by adjusting the Si concentration, dimethylsiloxane chain length, alkylene oxide type, etc., and any type can be selected depending on the type of air-curable compound and the matrix system. it can.
【0016】具体的には、各シリコーンメーカーより、
シリコーン界面活性剤、ウレタンフォーム用整泡剤、消
泡剤として販売されているもののなかから任意に選択で
きる。シリコーン系界面活性剤の配合量は、変成シリコ
ーン樹脂100重量部に対し、0.01〜5重量部が好
ましい。Specifically, from each silicone maker,
It can be arbitrarily selected from those sold as silicone surfactants, foam stabilizers for urethane foam, and defoamers. The amount of the silicone surfactant is preferably 0.01 to 5 parts by weight based on 100 parts by weight of the modified silicone resin.
【0017】(C)の空気硬化性化合物としては、空気
中の酸素によって重合する不飽和基を有する化合物が好
ましい。具体的には、桐油、アマニ油等の乾性油、およ
びそれらの変成物、ブタジエン、クロロプレン、イソプ
レン、1,3−ペンタジエン等のジエン系化合物を重合
または共重合させて得られる液状重合体およびそれらの
変成物が挙げられる。As the air-curable compound (C), a compound having an unsaturated group which is polymerized by oxygen in the air is preferable. Specifically, drying oils such as tung oil and linseed oil, and their modified products, butadiene, chloroprene, isoprene, and liquid polymers obtained by polymerizing or copolymerizing diene-based compounds such as 1,3-pentadiene, and the like. Metamorphosis.
【0018】空気硬化性化合物の配合量は、変成シリコ
ーン樹脂の100重量部に対して1〜20重量部で、1
重量部に満たないと表面タック改善効果が不十分で20
重量部を超えると、(B)のシリコーン界面活性剤、
(D)のポリオキシアルキレン重合体を添加した系にお
いても、表面硬度上昇が著しい。The amount of the air-curable compound is from 1 to 20 parts by weight based on 100 parts by weight of the modified silicone resin.
If the amount is less than 20 parts by weight, the effect of improving the surface tack is insufficient.
If the amount exceeds the weight part, the silicone surfactant of (B),
In the system to which the polyoxyalkylene polymer (D) is added, the surface hardness is significantly increased.
【0019】(D)のポリオキシアルキレン重合体とし
ては、アルキレンオキシドを重合させて得られる分子量
1,000〜30,000のポリオキシアルキレンであ
って、かつ加水分解性珪素基を有しない有機重合体が好
ましい。The polyoxyalkylene polymer (D) is a polyoxyalkylene having a molecular weight of 1,000 to 30,000 obtained by polymerizing an alkylene oxide and having no hydrolyzable silicon group. Coalescence is preferred.
【0020】この有機重合体としては、水酸基末端ポリ
オキシアルキレンの他、その誘導体が挙げられる。誘導
体としては末端水酸基をエーテル結合、エステル結合ウ
レタン結合などの結合を介してアルキル基、アルケニル
基などの炭化水素基で封止した重合体が挙げられる。ポ
リオキシアルキレン重合体の配合量としては、(A)の
変成シリコーン樹脂の100重量部対し、1〜150重
量部が好ましい。Examples of the organic polymer include a hydroxyl-terminated polyoxyalkylene and derivatives thereof. Examples of the derivative include a polymer in which a terminal hydroxyl group is sealed with a hydrocarbon group such as an alkyl group or an alkenyl group via a bond such as an ether bond or an ester bond urethane bond. The blending amount of the polyoxyalkylene polymer is preferably from 1 to 150 parts by weight based on 100 parts by weight of the modified silicone resin (A).
【0021】本発明の他の配合剤としては、硬化促進
剤、硬化遅延剤、可塑剤、充填剤染・顔料、紫外線吸収
剤、その他の添加剤を必要に応じて使用する。充填剤と
しては、炭酸カルシウム、タルク、カオリンなどの無機
充填剤を建築用シーリング材としてのペースト状適正な
チキソトロピー性付与のために変成シリコーン樹脂10
0重量部に対して150〜250重量部用いる。As other compounding agents of the present invention, a curing accelerator, a curing retarder, a plasticizer, a dye / pigment for a filler, an ultraviolet absorber, and other additives are used as required. As a filler, an inorganic filler such as calcium carbonate, talc, kaolin or the like is used as a modified silicone resin 10 in order to impart a proper thixotropic property as a paste as a building sealing material.
Use 150 to 250 parts by weight with respect to 0 parts by weight.
【0022】[0022]
【実施例】次に、本発明のシーリング材の実施例に基づ
き、具体的に説明する。 (実施例1〜3、比較例1〜2)Next, the present invention will be specifically described based on examples of the sealing material of the present invention. (Examples 1-3, Comparative Examples 1-2)
【0023】表1に示す基剤配合組成に従い、各成分を
バタフライミキサーにて混練した後、3本ロールにて分
散させる。その後バタフライミキサーにて再混合、脱気
し基剤とした。また、表1の硬化剤配合に従い、窒素気
流下硬化触媒、可塑剤、充填材をバタフライミキサーで
混合し、硬化剤とした。According to the base composition shown in Table 1, each component is kneaded with a butterfly mixer and then dispersed with three rolls. Thereafter, the mixture was remixed and degassed with a butterfly mixer to obtain a base. In addition, according to the curing agent formulation shown in Table 1, a curing catalyst, a plasticizer, and a filler were mixed with a butterfly mixer under a nitrogen stream to obtain a curing agent.
【0024】[0024]
【表1】 [Table 1]
【0025】上記方法で製造した基剤:硬化剤を10:
1の割合で混合し、以下(1)〜(4)に示す試験を行
った。なお、試験体としては、JIS A 1439引
張接着性試験における試験体を用い、接着面にはプライ
マーNEW80(日立化成ポリマー(株)製)を予め塗
付した。The base prepared by the above method: the curing agent is 10:
After mixing at a ratio of 1, the tests shown in the following (1) to (4) were performed. In addition, as a test body, a test body in a JIS A 1439 tensile adhesion test was used, and a primer NEW80 (manufactured by Hitachi Chemical Co., Ltd.) was previously applied to the bonding surface.
【0026】(1)引張接着性 JIS A 1439引張接着性試験に従い、50%伸
長時の引張応力(M50)最大引張応力(Tmax)、
破断時の伸び(Eb)を測定した。(1) Tensile adhesion According to JIS A 1439 tensile adhesion test, tensile stress at 50% elongation (M50), maximum tensile stress (Tmax),
The elongation at break (Eb) was measured.
【0027】(2)表面タック 23℃,50%で1日後、7日後の表面タックを指触に
て判定した。(2) Surface tack The surface tack after 1 day and 23 days at 23 ° C. and 50% was judged by finger touch.
【0028】(3)耐候性試験:サンシャインウエザー
メータ(W.O.M.スガ試験機(株)製)にて、所定
時間照射した後の劣化状況を観察した。(3) Weather resistance test: The state of deterioration after irradiation for a predetermined time was observed with a sunshine weather meter (WOM Suga Test Machine Co., Ltd.).
【0029】(5)伸縮繰り返し試験:サンシャインウ
エザーメータ(スガ試験機(株)製)にて、所定時間照
射した後、±30%の伸縮繰り返し試験を23℃で10
00回行い、表面の状態を観察した。(5) Repetition test of expansion and contraction: After irradiation with a sunshine weather meter (manufactured by Suga Test Instruments Co., Ltd.) for a predetermined time, a repetition test of ± 30% expansion and contraction was performed at 23 ° C.
This was performed 00 times, and the state of the surface was observed.
【0030】試験結果を以下表2に示す。The test results are shown in Table 2 below.
【0031】[0031]
【表2】 [Table 2]
【0032】[0032]
【発明の効果】変成シリコーン樹脂に空気硬化性化合物
を添加したした系において、特定のシリコーン化合物と
高分子可塑剤を添加することによって系内の相溶性が向
上し、経時後の硬化物表面の硬度上昇が緩和される。As described above, in a system in which an air-curable compound is added to a modified silicone resin, the compatibility in the system is improved by adding a specific silicone compound and a high-molecular plasticizer, and the surface of the cured product after aging is improved. The increase in hardness is reduced.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C09K 3/10 C08L 83/10 - 83/12 C08L 71/02 - 71/04 ──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int. Cl. 7 , DB name) C09K 3/10 C08L 83/10-83/12 C08L 71/02-71/04
Claims (1)
(または)加水分解性基を有し、シロキサン結合を形成
することにより架橋しうる珪素含有基を少なくとも1個
有するゴム系有機重合体100重量部に対し、(B)メ
チルポリシロキサン、ポリアルキレンオキサイドから構
成されるシリコーン系界面活性剤0.01〜5重量部、
(C)空気硬化性化合物1〜20重量部、(D)高分子
可塑剤として分子量1,000以上のポリオキシアルキ
レン重合体を含有してなる建築用変成シリコーン系シー
リング材組成物。1. A rubber-based organic polymer (A) having a hydroxyl group and / or a hydrolyzable group bonded to a silicon atom and having at least one silicon-containing group which can be crosslinked by forming a siloxane bond. (B) 0.01 to 5 parts by weight of a silicone surfactant composed of (B) methylpolysiloxane and polyalkylene oxide,
A modified silicone sealant composition for construction comprising (C) 1 to 20 parts by weight of an air-curable compound, and (D) a polyoxyalkylene polymer having a molecular weight of 1,000 or more as a polymer plasticizer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3899599A JP3008284B1 (en) | 1999-01-08 | 1999-01-08 | Modified silicone sealant for construction |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3899599A JP3008284B1 (en) | 1999-01-08 | 1999-01-08 | Modified silicone sealant for construction |
Publications (2)
Publication Number | Publication Date |
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JP3008284B1 true JP3008284B1 (en) | 2000-02-14 |
JP2000204346A JP2000204346A (en) | 2000-07-25 |
Family
ID=12540726
Family Applications (1)
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JP3899599A Expired - Fee Related JP3008284B1 (en) | 1999-01-08 | 1999-01-08 | Modified silicone sealant for construction |
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Country | Link |
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JP (1) | JP3008284B1 (en) |
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Publication number | Priority date | Publication date | Assignee | Title |
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ATE532828T1 (en) | 2006-01-18 | 2011-11-15 | Kaneka Corp | CURDABLE COMPOSITION |
JP5275822B2 (en) * | 2009-01-08 | 2013-08-28 | 鹿島建設株式会社 | Apparatus and method for measuring tensile stress of sealing material |
JP5597070B2 (en) * | 2010-09-06 | 2014-10-01 | コニシ株式会社 | Sealant composition |
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1999
- 1999-01-08 JP JP3899599A patent/JP3008284B1/en not_active Expired - Fee Related
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