JPH0223586B2 - - Google Patents
Info
- Publication number
- JPH0223586B2 JPH0223586B2 JP13124984A JP13124984A JPH0223586B2 JP H0223586 B2 JPH0223586 B2 JP H0223586B2 JP 13124984 A JP13124984 A JP 13124984A JP 13124984 A JP13124984 A JP 13124984A JP H0223586 B2 JPH0223586 B2 JP H0223586B2
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- pot life
- solvent
- polyvinyl acetate
- compound
- 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
Links
- 239000000853 adhesive Substances 0.000 claims description 44
- 230000001070 adhesive effect Effects 0.000 claims description 44
- 150000001875 compounds Chemical class 0.000 claims description 21
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims description 20
- 239000004606 Fillers/Extenders Substances 0.000 claims description 15
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 14
- 239000011118 polyvinyl acetate Substances 0.000 claims description 14
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 239000002904 solvent Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000009408 flooring Methods 0.000 description 5
- -1 polyoxyethylene diglycerin monostearate Polymers 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000010425 asbestos Substances 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 229910052895 riebeckite Inorganic materials 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000002314 glycerols Chemical class 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-hydroxyoctadecanoic acid Chemical group CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 235000010338 boric acid Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical group CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 1
- BYNVYIUJKRRNNC-UHFFFAOYSA-N docosanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCCCCCCCC(O)=O BYNVYIUJKRRNNC-UHFFFAOYSA-N 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid ester group Chemical group C(CCCCCCCCCCC)(=O)O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 229940093625 propylene glycol monostearate Drugs 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical group CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
本発明は溶剤型ポリ酢酸ビニル系接着剤の可使
時間延長剤に関するものである。更に詳しくは合
成樹脂、特にポリ塩化ビニル系床材を下地に接着
施工する際に用いられる溶剤型ポリ酢酸ビニル系
接着剤の可使時間を長くし、良好な作業性を付与
する可使時間延長剤に関するものである。尚、本
発明にいう可使時間とは次のようなものである。
すなわち耐水ベニヤかまたは石綿板上に接着剤を
JIS A―5536に規定するクシ目ゴテにて300g/
m2塗布し、この上に10×10cmに切つたJIS A―
5705に規定するタイルを置き、タイルの上に200
gの分銅を10秒間のせた後直ちにタイルを剥し、
目視判定にて接着剤がタイル裏面のグルーライン
(接着剤のクシ山の部分がタイル裏面と接触した
線状の部分)の面積の50%以上に付着しているま
での時間をさす。
合成樹脂、特にポリ塩化ビニルからなる床材を
モルタルなどの下地に貼着するのにポリ酢酸ビニ
ル系の接着剤が使用されている。
この種の接着剤は他のものに比べ比較的安価で
あること、床材の素材であるポリ塩化ビニルなど
に対し良好な親和性を有すること、取扱いが容易
であること等の種々の利点を有するものである。
そして、この種の接着剤は大別してエマルジヨン
と呼ばれる水性タイプと有機溶剤を媒介とする溶
剤タイプの2種に分けられる。前者は環境上好ま
しい反面比較的接着強度が弱く耐水性にも劣つて
いる。したがつて接着強度や耐水性の必要な場所
には溶剤タイプのものが欠かせない存在となつて
いる。
上記溶剤型接着剤はエマルジヨン型の接着剤と
異なり、下地に塗布すると溶剤が揮散することに
より接着剤自体が固化するものである。
そして、この溶剤の揮散はかなり速い速度で行
われるので接着剤を下地に塗布後この上に床材を
貼るまでの時間的余裕(可使時間)が短く、接着
のタイミングが遅れると床材の剥離、反り、ふく
れ等の問題を起し、接着作業にも種々の制約が伴
うなど好ましくなかつた。
この可使時間は夏場の高温時において短かくな
るが、冬場の気温が0℃以下になる低温時におい
ても短かくなることが知られている。この冬場の
現象についてはいかなる理由によるものかは判別
していないが次のように考えられている。すなわ
ち低温になると組成物中に混合されている種々の
添加剤の相溶性が低下し、系のバランスがくずれ
直接溶剤が揮散しやすくなるためと推察されてい
る。
この問題を解決する試みとして、可使時間延長
剤を添加することが、従来から行われている。そ
して、可使時間延長剤としては、過去に次のよう
なものが提案されているが、広い温度範囲にわた
つて要求される可使時間を与えるものはいまだに
見出されていない。
(i) アミン類:ステアリルアミン、ラウリルアミ
ン等
(ii) グリセリンエステル類:グリセリンモノステ
アレート、グリセリンモノベヘネート、ジグリ
セリンモノ(ジ)ステアレート、ポリオキシエ
チレンジグリセリンモノステアレート等
(iii) プロピレングリコールエステル類:プロピレ
ングリコールモノステアレート等
(iv) 一般的界面活性剤類:ポリオキシアルキレン
アルキルエーテル、ソルビタンエステル、アル
キルサルフエート、アルキルホスフエート等
上記のうち、アミン類およびグリセリンエステ
ル類は室温から夏場の高温域では効果がある。し
かし0℃以下の低温域においては効果がなく可使
時間が短かくなる。したがつて寒冷地に適さな
い。プロピレングリコールエステル類は高温域に
おいてもあまり顕著な効果は示さない。界面活性
剤類は室温から高温域にかけて効果を示さない。
更にこれらの化合物は接着剤の粘度を低下させ、
タツク(粘着性)を低下させる。一般的にいつ
て、接着剤溶液に透明に溶解するものは効果がな
い。また、アルキレンオキサイドを高モル付加し
たものや不飽和基を含有するものも溶解度が高く
効果が少ない。
本発明は前記従来の問題を解決し、夏場から冬
場までの広い温度範囲で、特に低温においても良
好な可使時間延長効果を奏する溶剤型ポリ酢酸ビ
ニル系接着剤用の可使時間延長剤を提供するもの
である。
本発明の可使用時間延長剤は、溶剤型ポリ酢酸
ビニル系接着剤が特に夏場の高温時又は冬場の低
温時に、ポリ酢酸ビニル系接着剤を塗布し、後こ
の上に床材等を貼る場合に、接着剤の溶剤が揮散
したり、接着剤自体が固化したりする傾向が甚だ
しく、接着剤を良好な接着状態で使用する時間が
極めて短時間であるため、接着操作に支障を来
す。本剤を溶剤型ポリ酢酸ビニル系接着剤に加え
ることにより、夏場から冬場にかけて広い温度範
囲において、上記接着剤を長時間良好な接着性の
状態に保持する接着剤添加剤である。
すなわち本発明は、
1 下記一般式()で示される溶剤型ポリ酢酸
ビニル系接着剤組成物用可使時間延長剤。
〔但し、式中Y1,Y2はHまたはCORを表わ
し、Rは炭素数11〜21のアルキル基またはヒド
ロキシアルキル基を表わす。〕
および
2 下記一般式()で示される化合物と平均付
加モル数が0.5〜1.5モルであるステアリルアル
コールエチレンオキサイド付加物(化合物
()と略)とからなり、かつ前者の含有率が
50重量%以上である溶剤型ポリ酢酸ビニル系接
着剤組成物用可使時間延長剤。
〔但し、式中Y1,Y2はHまたはCORを表わ
し、Rは炭素数11〜21のアルキル基またはヒド
ロキシアルキル基を表わす。〕
をその要旨とするものである。
一般式()で示される化合物はホウ酸とグリ
セリンと脂肪酸(または脂肪酸ハライド)とを常
法によりエステル化することから得られる有機ホ
ウ酸エステルであり、好適な具体例としては、
CORにおいてRがC11のラウリル酸残基、C13の
ミリスチン酸残基、C15のパルミチン酸残基、C17
のステアリン酸残基、C17のヒドロキシステアリ
ン酸残基、C21のベヘニン酸残基である化合物が
あげられる。
更に本発明で使用しうる平均付加モル数が0.5
〜1.5モルであるステアリルアルコールエチレン
オキサイド付加物(化合物)とはステアリルア
ルコール1モルにエチレンオキサイドが平均で
0.5〜1.5モル付加した化合物を意味し、未反応ス
テアリルアルコールやエチレンオキサイドの2モ
ル以上付加物等が実質的に含まれていても良い。
ここでいうステアリルアルコールとは、炭素数
が18のステアリルアルコールを主成分とする固型
アルコールの混合物であり、マツコウ鯨油、牛脂
等の動物油、大豆油等の植物油などの天然油脂を
原料とし接触還元あるいは炭素数18のアルキル基
を多量に含む不飽和アルコールの水素添加により
得られる種々の純度のステアリルアルコールを意
味し、該ステアリルアルコールが50重量%以上含
まれる固型アルコールであれば本発明に使用しう
る。
化合物()はエチレンオキサイドの平均付加
モル数が2モル以上になると接着剤との相溶性を
増し、顕著な効果を示さなくなる。また平均付加
モル数が0.4モル以下であると未反応の原料ステ
アリルアルコール分が増加し可使時間延長効果が
少ない。
化合物()のアルキル基の炭素数が16以下で
は接着剤との相溶性を増し好ましくなく、炭素数
が20以上では逆に接着剤との相溶性が悪くなるの
か大きな結晶が析出し効果がない。
一般式()の化合物は広い温度範囲で可使時
間を延長することができる。一般式()の化合
物と化合物()とを併用することにより、より
一層の可使時間を延長することができるとともに
良好なタツク性も保持できる。また一般式()
の化合物と化合物()との混合物を使用する場
合、前者を50重量%以上含有することによりすぐ
れた可使時間延長効果を与えるとともに、タツク
性も良好な接着剤組成物とすることができる。
一般式()の化合物が50重量%以下の時は、
可使時間延長効果は有するもののタツクが不足し
作業性に支障をきたす。
このような化合物は溶剤型ポリ酢酸ビニル系の
接着剤に添加混合される。この種の接着剤に用い
られるポリ酢酸ビニル系樹脂は、酢酸ビニルの単
独重合体のほか、酢酸ビニルとエチレン、プロピ
レン等のオレフイン、あるいはアクリル酸、メタ
クリル酸、マレイン酸等の不飽和酸あるいはその
アルキルエステル塩化ビニル等との共重合体で、
この共重合体中酢酸ビニルが50重量%以上含まれ
ているものである。
有機溶剤としては前述のような樹脂を溶解しう
るものであれば特に限定はない。工業的に安価に
入手でき比較的安全であるアルコール類、特にメ
タノール、エタノールが良く用いられる。そのほ
かには酢酸エチル、トルエン、アセトンなどが例
示できる。
またこの種の接着剤には通常炭酸カルシユム、
タルク、クレー、アスベストなどのフイラーやロ
ジン、変性ロジン、石油樹脂などの粘着付与剤な
どのほか、一般に使用されている添加剤類を使用
することもなんらさしつかえない。
本発明の可使時間延長剤は上述のような接着剤
のポリ酢酸ビニル系樹脂に対し0.05〜5重量%を
接着剤の製造時に通常添加する。もちろんこの場
合これに従来公知の可使時間延長剤を併用するこ
ともなんらさしつかえない。そして本発明の可使
時間延長剤は前述のごとく(1)夏場の高温時に可使
時間が延長され良好な作業性を与えること、(2)0
℃以下の低温時においても可使時間が延長され良
好な作業性を与えること、(3)タツクの良好な接着
剤組成物を与えること、等の優れた効果を有する
ものである。
次に実施例について本発明をより具体的に説明
する。
実施例1〜9及び比較例1〜10
まずポリ酢酸ビニルのメタノール溶液(固型分
50%)100gに表―1に示す置換基を変えた式
()の化合物5種、及び式()と化合物()
の混合比を変えた4種の可使時間延長剤をそれぞ
れ2g、メタノール20gを加えて混合する。更に
炭酸カルシウム50g、アスベスト50gを加えて撹
拌混合して接着剤を得た。一方、尚比較のために
表―2及び表―3に示す従来の可使時間延長剤を
用いて同様に接着剤10種を得、これを比較例とし
た。これらの接着剤について最初に定義した要領
で25℃、0℃、−5℃における可使時間を測定し
た。その結果をそれぞれの表に併記した。
これらの表から本発明の可使時間延長剤を用い
たものは高温から低温までの広い温度範囲におい
て良好な可使時間延長効果がみられ、特に式
()の化合物と化合物()とを併用したもの
の効果が顕著であることがわかる。そしてこのも
のはタツク性も良好であつた。
タツク性;0℃における可使時間測定時に、粘着
の強さを官能して判定し、その最良値をもつ
てそれぞれのサンプル間の比較をし、相対的
に良好なものを〇、やや劣るものを△、劣る
ものを×とした。
The present invention relates to a pot life extender for solvent-type polyvinyl acetate adhesives. More specifically, we extend the pot life of synthetic resins, especially solvent-based polyvinyl acetate adhesives used when bonding polyvinyl chloride flooring materials to the base, and provide good workability. This is related to drugs. Note that the pot life as referred to in the present invention is as follows.
i.e. adhesive on waterproof veneer or asbestos board.
300g/ with a comb trowel specified in JIS A-5536
JIS A- coated with m2 and cut into 10 x 10 cm pieces on top.
Place a tile specified in 5705 and place 200 on top of the tile.
After placing a weight of g for 10 seconds, immediately remove the tile.
The time it takes for the adhesive to adhere to 50% or more of the area of the glue line on the back of the tile (the linear part where the comb of the adhesive contacts the back of the tile) as determined by visual inspection. Polyvinyl acetate-based adhesives are used to adhere flooring materials made of synthetic resin, particularly polyvinyl chloride, to a base such as mortar. This type of adhesive has various advantages such as being relatively inexpensive compared to other adhesives, having good affinity for flooring materials such as polyvinyl chloride, and being easy to handle. It is something that you have.
This type of adhesive can be roughly divided into two types: an aqueous type called an emulsion and a solvent type using an organic solvent as a medium. While the former is environmentally preferable, it has relatively weak adhesive strength and poor water resistance. Therefore, solvent-based adhesives have become indispensable in areas where adhesive strength and water resistance are required. The above-mentioned solvent-based adhesive is different from an emulsion-based adhesive in that when it is applied to a base, the solvent evaporates and the adhesive itself solidifies. Since this solvent volatilizes at a fairly fast rate, there is only a short amount of time (pot life) between applying the adhesive to the base and pasting the flooring on top, and if the timing of adhesion is delayed, the flooring Problems such as peeling, warping, and blistering were caused, and various restrictions were attached to adhesion work, which was undesirable. It is known that this pot life is shortened at high temperatures in the summer, but also shortened at low temperatures in the winter when the temperature is below 0°C. The reason for this winter phenomenon has not been determined, but it is thought to be as follows. In other words, it is assumed that this is because when the temperature becomes low, the compatibility of various additives mixed in the composition decreases, the balance of the system is lost, and the solvent becomes more likely to volatilize directly. As an attempt to solve this problem, adding a pot life extender has conventionally been carried out. Although the following pot life extenders have been proposed in the past, no one has yet been found that provides the required pot life over a wide temperature range. (i) Amines: stearylamine, laurylamine, etc. (ii) Glycerin esters: glycerin monostearate, glycerin monobehenate, diglycerin mono(di)stearate, polyoxyethylene diglycerin monostearate, etc. (iii) Propylene glycol esters: propylene glycol monostearate, etc. (iv) General surfactants: polyoxyalkylene alkyl ether, sorbitan ester, alkyl sulfate, alkyl phosphate, etc. Among the above, amines and glycerin esters are used at room temperature. It is effective in high temperature areas in summer. However, in the low temperature range below 0°C, it is not effective and the pot life is shortened. Therefore, it is not suitable for cold regions. Propylene glycol esters do not show very significant effects even at high temperatures. Surfactants have no effect in the room temperature to high temperature range.
Furthermore, these compounds reduce the viscosity of the adhesive,
Reduces tack (tackiness). Generally speaking, those that dissolve transparently in the adhesive solution are ineffective. Furthermore, those with a high molar addition of alkylene oxide and those containing unsaturated groups also have high solubility and are less effective. The present invention solves the above conventional problems and provides a pot life extender for solvent-based polyvinyl acetate adhesives that exhibits a good pot life extension effect over a wide temperature range from summer to winter, especially at low temperatures. This is what we provide. The usable life extender of the present invention is used when a solvent-based polyvinyl acetate adhesive is applied especially at high temperatures in the summer or at low temperatures in the winter. Furthermore, the solvent in the adhesive tends to volatilize and the adhesive itself tends to solidify, and the time the adhesive can be used in a good bonding state is extremely short, which hinders the bonding operation. By adding this agent to a solvent-based polyvinyl acetate adhesive, it is an adhesive additive that maintains the adhesive in a good adhesive state for a long time over a wide temperature range from summer to winter. That is, the present invention provides: 1. A pot life extender for a solvent-type polyvinyl acetate adhesive composition represented by the following general formula (). [However, in the formula, Y 1 and Y 2 represent H or COR, and R represents an alkyl group or hydroxyalkyl group having 11 to 21 carbon atoms. ] and 2 consisting of a compound represented by the following general formula () and a stearyl alcohol ethylene oxide adduct (abbreviated as compound ()) with an average number of added moles of 0.5 to 1.5 moles, and the content of the former is
A pot life extender for solvent-based polyvinyl acetate adhesive compositions containing 50% by weight or more. [However, in the formula, Y 1 and Y 2 represent H or COR, and R represents an alkyl group or hydroxyalkyl group having 11 to 21 carbon atoms. ] Its gist is as follows. The compound represented by the general formula () is an organic boric acid ester obtained by esterifying boric acid, glycerin, and fatty acid (or fatty acid halide) by a conventional method. Preferred specific examples include:
In COR, R is C11 lauric acid residue, C13 myristic acid residue, C15 palmitic acid residue, C17
Examples include compounds having a stearic acid residue at C17 , a hydroxystearic acid residue at C17, and a behenic acid residue at C21 . Furthermore, the average number of added moles that can be used in the present invention is 0.5
Stearyl alcohol ethylene oxide adduct (compound) is ~1.5 moles, which means that 1 mole of stearyl alcohol contains ethylene oxide on average.
It means a compound added with 0.5 to 1.5 moles, and may substantially contain unreacted stearyl alcohol, an adduct of 2 moles or more of ethylene oxide, etc. Stearyl alcohol here is a mixture of solid alcohols whose main component is stearyl alcohol with 18 carbon atoms, and is catalytically reduced using natural fats and oils such as animal oils such as pine whale oil and beef tallow, and vegetable oils such as soybean oil. Alternatively, it refers to stearyl alcohol of various purity obtained by hydrogenation of unsaturated alcohol containing a large amount of alkyl groups having 18 carbon atoms, and any solid alcohol containing 50% by weight or more of stearyl alcohol can be used in the present invention. I can do it. When the average number of moles of ethylene oxide added is 2 moles or more, the compound () becomes more compatible with the adhesive and no longer exhibits any significant effect. Furthermore, if the average number of moles added is less than 0.4 moles, the unreacted raw material stearyl alcohol content will increase, and the pot life extension effect will be small. If the number of carbon atoms in the alkyl group of the compound () is less than 16, it will increase the compatibility with the adhesive, which is undesirable. If the number of carbon atoms is more than 20, the compatibility with the adhesive will deteriorate, or large crystals will precipitate, making it ineffective. . The compound of general formula () can extend pot life over a wide temperature range. By using the compound of the general formula () and the compound () together, the pot life can be further extended, and good tackiness can also be maintained. Also general formula ()
When using a mixture of the compound (2) and the compound (2), by containing the former in an amount of 50% by weight or more, it is possible to obtain an adhesive composition that not only has an excellent pot life extension effect but also has good tackiness. When the compound of general formula () is 50% by weight or less,
Although it has the effect of extending pot life, it lacks tact, which hinders workability. Such a compound is added to and mixed with a solvent-type polyvinyl acetate adhesive. The polyvinyl acetate resin used in this type of adhesive is a homopolymer of vinyl acetate, vinyl acetate and olefins such as ethylene or propylene, or unsaturated acids such as acrylic acid, methacrylic acid, maleic acid, or their like. Copolymer with alkyl ester vinyl chloride etc.
This copolymer contains 50% by weight or more of vinyl acetate. The organic solvent is not particularly limited as long as it can dissolve the above-mentioned resin. Alcohols, especially methanol and ethanol, which are industrially available at low cost and relatively safe, are often used. Other examples include ethyl acetate, toluene, and acetone. This type of adhesive also usually contains calcium carbonate,
In addition to fillers such as talc, clay, and asbestos, and tackifiers such as rosin, modified rosin, and petroleum resin, there is nothing wrong with using commonly used additives. The pot life extender of the present invention is usually added in an amount of 0.05 to 5% by weight to the polyvinyl acetate resin of the adhesive as described above during the production of the adhesive. Of course, in this case, it is also possible to use a conventionally known pot life extender in combination. As mentioned above, the pot life extender of the present invention has the following properties: (1) the pot life is extended at high temperatures in summer and provides good workability;
It has excellent effects such as extending pot life and providing good workability even at low temperatures below .degree. C., and (3) providing an adhesive composition with good tack. Next, the present invention will be described in more detail with reference to Examples. Examples 1 to 9 and Comparative Examples 1 to 10 First, a methanol solution of polyvinyl acetate (solid content
50%) 100g of 5 compounds of formula () with different substituents shown in Table 1, and formula () and compound ()
2g of each of the four types of pot life extenders with different mixing ratios and 20g of methanol were added and mixed. Further, 50 g of calcium carbonate and 50 g of asbestos were added and mixed with stirring to obtain an adhesive. On the other hand, for comparison, 10 types of adhesives were similarly obtained using conventional pot life extenders shown in Tables 2 and 3, and these were used as comparative examples. The pot life of these adhesives at 25°C, 0°C, and -5°C was measured as originally defined. The results are also listed in each table. From these tables, it can be seen that products using the pot life extender of the present invention have a good pot life extension effect in a wide temperature range from high to low temperatures, and in particular, when used in combination with the compound of formula () and compound () It can be seen that the effect is remarkable. This material also had good tackiness. Tackiness: When measuring the pot life at 0°C, the strength of adhesion is determined by sensory evaluation, and the best value is used to compare each sample. The results were evaluated as △, and those that were inferior were evaluated as ×.
【表】【table】
【表】【table】
【表】【table】
Claims (1)
ビニル系接着剤組成物用可使時間延長剤。 〔但し、式中Y1,Y2はHまたはCORを表わ
し、Rは炭素数11〜21のアルキル基またはヒドロ
キシアルキル基を表わす。〕 2 下記一般式()で示される化合物と平均付
加モル数が0.5〜1.5モルであるステアリルアルコ
ールエチレンオキサイド付加物とからなり、かつ
前者の含有率が50重量%以上である溶剤型ポリ酢
酸ビニル系接着剤組成物用可使時間延長剤。 〔但し、式中Y1,Y2はHまたはCORを表わ
し、Rは炭素数11〜21のアルキル基またはヒドロ
キシアルキル基を表わす。〕[Claims] 1. A pot life extender for a solvent-type polyvinyl acetate adhesive composition represented by the following general formula (). [However, in the formula, Y 1 and Y 2 represent H or COR, and R represents an alkyl group or hydroxyalkyl group having 11 to 21 carbon atoms. ] 2 A solvent-type polyvinyl acetate consisting of a compound represented by the following general formula () and a stearyl alcohol ethylene oxide adduct with an average number of added moles of 0.5 to 1.5 moles, and in which the content of the former is 50% by weight or more. A pot life extender for adhesive compositions. [However, in the formula, Y 1 and Y 2 represent H or COR, and R represents an alkyl group or hydroxyalkyl group having 11 to 21 carbon atoms. ]
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13124984A JPS619476A (en) | 1984-06-26 | 1984-06-26 | Working life prolonging agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13124984A JPS619476A (en) | 1984-06-26 | 1984-06-26 | Working life prolonging agent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS619476A JPS619476A (en) | 1986-01-17 |
JPH0223586B2 true JPH0223586B2 (en) | 1990-05-24 |
Family
ID=15053488
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13124984A Granted JPS619476A (en) | 1984-06-26 | 1984-06-26 | Working life prolonging agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS619476A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8617004D0 (en) * | 1986-07-11 | 1986-08-20 | Bp Chem Int Ltd | Polymer composition |
US4906680A (en) * | 1987-04-14 | 1990-03-06 | Bridgestone Corporation | Rubber composition and steel cord-rubber composite body |
US6337742B2 (en) | 1988-04-28 | 2002-01-08 | Pruftechnik Dieter Busch Ag | Device for ascertaining the relative position of a reference axis of an object relative to a reference beam, in particular a laser beam |
DE3814466A1 (en) | 1988-04-28 | 1989-11-09 | Busch Dieter & Co Prueftech | METHOD AND DEVICE FOR DETERMINING THE RELATIVE POSITION OF A REFERENCE AXIS OF AN OBJECT WITH REGARD TO A REFERENCE BEAM, ESPECIALLY A LASER BEAM |
-
1984
- 1984-06-26 JP JP13124984A patent/JPS619476A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS619476A (en) | 1986-01-17 |
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