JPS649341B2 - - Google Patents
Info
- Publication number
- JPS649341B2 JPS649341B2 JP14902480A JP14902480A JPS649341B2 JP S649341 B2 JPS649341 B2 JP S649341B2 JP 14902480 A JP14902480 A JP 14902480A JP 14902480 A JP14902480 A JP 14902480A JP S649341 B2 JPS649341 B2 JP S649341B2
- Authority
- JP
- Japan
- Prior art keywords
- vinyl
- ethylene
- composition
- weight
- backing
- 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
- 239000000203 mixture Substances 0.000 claims description 21
- 239000000839 emulsion Substances 0.000 claims description 18
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 14
- 229920002554 vinyl polymer Polymers 0.000 claims description 13
- 229920005670 poly(ethylene-vinyl chloride) Polymers 0.000 claims description 12
- 239000011256 inorganic filler Substances 0.000 claims description 9
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 229920001567 vinyl ester resin Polymers 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
- 239000000945 filler Substances 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- 239000006228 supernatant Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims 1
- 239000003063 flame retardant Substances 0.000 description 13
- 239000000835 fiber Substances 0.000 description 12
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 11
- -1 polypropylene Polymers 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 8
- 230000006866 deterioration Effects 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 238000002845 discoloration Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 238000005562 fading Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920006174 synthetic rubber latex Polymers 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- 206010000369 Accident Diseases 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 239000004114 Ammonium polyphosphate Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 1
- 229920001276 ammonium polyphosphate Polymers 0.000 description 1
- QBLDFAIABQKINO-UHFFFAOYSA-N barium borate Chemical compound [Ba+2].[O-]B=O.[O-]B=O QBLDFAIABQKINO-UHFFFAOYSA-N 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- 229920001600 hydrophobic polymer Polymers 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 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
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- UTSYWKJYFPPRAP-UHFFFAOYSA-N n-(butoxymethyl)prop-2-enamide Chemical compound CCCCOCNC(=O)C=C UTSYWKJYFPPRAP-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 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
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Landscapes
- Carpets (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は敷物のバツキング用組成物に関する。
さらに詳しくはビニルエステル―エチレン―塩化
ビニル系共重合体を含むエマルジヨンと塩基性無
機質充填剤を配合してなる敷物のバツキング用組
成物に関する。
従来より敷物として種々の組織や構造のものが
使われており近年は製造工程の簡便性、経済性な
どの理由からパイルを基布に植込んだタフテツド
カーペツトと称されるものやウエブをニードルパ
ンチング法により機械的に絡めたニードルパンチ
カーペツトが多く使用されている。かかる敷物は
パイルまたはウエブが単に機械的に交絡されたも
のであるために形状が不安定でそのままでは実用
に供しえないものである。そこで通常は敷物の表
面または裏面に天然ゴムあるいは合成ゴムラテツ
クスや合成樹脂エマルジヨンを単独もしくは配合
物の形で塗布乾燥して敷物としての抜糸強度や寸
法安定性を付与せしめる加工が行われている。こ
れらの敷物類は住宅をはじめとして車輛、航空
機、船舶などの各種の用途に供されるが近年では
火災事故防止のためかかる敷物に対して難燃性の
規制が強化されつつある。このため繊維そのもの
の難燃化およびバツキング剤での難燃化など種々
の方法が構じられているが、経済性や技術面など
の点からバツキング剤による難燃化が現在主流と
なつている。
これらの用途の中で車輛用、特に自動車の内装
用において近年装着される材料としての敷物も難
燃規制が適用され、しかもこの他に最近さらに耐
熱耐光性能の基準も強化されてきたために特に難
燃化と共に耐熱耐光性への対処が必要となつてい
る。自動車内装用として多く使われているニード
ルパンチカーペツトにおいては、それを構成する
繊維素材は従来塩化ビニルや塩化ビニリデン系繊
維などと他の繊維の混紡であつたが、軽量化など
の必要から最近になつてポリプロピレン繊維に転
換されたことは、かかる分野における難燃強化の
ニーズに対してポリプロピレンが燃えやすい素材
であるため、従来以上にますますバツキング剤で
の性能改善がきびしく要求されるところになつて
いる。これがため従来使われていたバツキング剤
の合成ゴムラテツクス例えばスチレン―ブタジエ
ン共重合ラテツクスでは必然的に難燃剤の配合量
を多くしなければならないが、この方法では難燃
化に有効であつても本来バツキングの目的である
パイルの抜糸防止形状の安定化の点で補強効果が
著しく損われるという欠点がある。かかる事情か
ら従来の合成ゴムラテツクスにかわつて最近はビ
ールエステル―エチレン―塩化ビニル系共重合体
エマルジヨンが次第に多く使用されるようになつ
ている。ビニルエステル―エチレン―塩化ビニル
系共重合体エマルジヨンは分子内に多くのハロゲ
ンを有しており、特に高ハロゲン含有量の共重合
体をバツキング剤に使用した場合は該共重合体自
身自消性であるためバツキング剤での難燃化が容
易であり、しかも難燃剤量が少なくても目的を達
する事ができるものである。本来の抜糸強度の付
与および形状の安定化の保持はもちろんの事、ま
た該共重合体が疎水性ポリマーである事によるす
ぐれた耐水強度を与える事も可能である。更に自
動車用敷物としても必要性能のうち、上記難燃
性、抜糸強度、形状安定性、耐水強度だけでなく
一方耐光性に関しても良好なる性能が要求され
る。例えば窓ガラス越しの太陽の軸射熱や光線に
対して敷物の特に強度低下による形くずれなど性
能劣化をきたすことのないバツキング剤が要求さ
れる。そこで近年該敷物の耐光性促進試験として
通常行われている紫外線フエードメーターによる
試験法を更にきびしい条件で試験を行なう試験規
格の強化が行われている。例えば試験用温度条件
として63℃から83℃に上げられたきびしいものと
なつている。このきびしい試験規格においても敷
物の繊維自体の劣化や形態くずれおよび変退色な
どを起す事のないバツキング剤の性能のものが要
求される。このような事から、本発明者らはビニ
ルエステル―エチレン―塩化ビニル系共重合体の
本来の有する敷物への性能を損なう事なく更に耐
光性の改良について種々検討の結果、塩基性無機
質充填剤を添加する事により難燃性、抜糸強度、
形状安定性、耐水性などの性能を維持して更に耐
光性が著しく優れるバツキング用組成物を見い出
し、本発明を完成するに至つた。
即ち本発明はビニルエステル―エチレン―塩化
ビニル系共重合体エマルジヨンおよび塩基性無機
質充填剤を必須成分として必要に応じて難燃剤、
分散剤、増粘剤などを配合してなる耐光性の優れ
た敷物のバツキング用組成物を提供するものであ
る。本発明のバツキング用組成物に使用される主
体となるバインダーはビニルエステル―エチレン
―塩化ビニル系共重合体エマルジヨンであり共重
合体の構成モノマー組成比はビニルエステル:エ
チレン:塩化ビニル=10〜55:5〜30:30〜75重
量比である。ビニルエステルは酢酸ビニルが好ま
しい。またビニルエステルとしてプロピオン酸ビ
ニル、バーサテイツク酸ビニルなどもある。ま
た、ビニルエステルの一部をアクリル酸エステ
ル、メタクリル酸エステルに置き換えビニルエス
テル特に好ましくは酢酸ビニルとの併用であつて
もよい。また、該共重合体に(メタ)アクリル
酸、マレイン酸モノエステル、N―メチロールア
クリルアミド、N―ブドキシメチルアクリルアミ
ド、アクリルアミド、グリシジルメタクリレー
ト、ヒドロキシエチルアクリレートなどの官能性
ビニルモノマーの少量を共重合させた共重合体エ
マルジヨンでも良い。これらの共重合体エマルジ
ヨンはいずれも通常のエマルジヨンの製造法によ
つて得られるものである。
本発明に用いる塩基性無機質充填剤としては炭
酸カルシウム、水酸化アルミニウム、酸化マグネ
シウム、タルク、亜鉛華、水酸化カルシウムなど
の金属酸化物、水酸化物、炭酸塩など通常市販さ
れているものであり、その使用量はビニルエステ
ル―エチレン―塩化ビニル系共重合体エマルジヨ
ンの固型分100重量部に対して30重量部〜160重量
部であり、好ましくは60〜100重量部である。該
塩基性無機質充填剤は1種または2種以上で用い
られる。この場合、該塩基性無機質充填剤の使用
量が該範囲より少ないとすぐれた耐光性が得られ
難く、また多いと物理強度の低下をきたす。
バツキング用組成物に使用するエマルジヨンは
塩基性物質の添加に対して増粘したり凝固する事
のないようにエマルジヨン自体の安定性が要求さ
れる。従つてバツキングして得られる敷物の上記
の性能特に耐光性を充分に付与し、かつ該共重合
体エマルジヨンの安定性を維持し、バツキング組
成物としての性能と作業性をバランスさせる必要
がある。
かかる理由から、本発明で使用する塩基性無機
質充填剤は具体的には該充填剤の10gを40gのイ
オン交換水にて分散せしめた上澄液のPHが8〜9
の範囲にあるような中等度の塩基性を有するもの
が好ましく、この場合該PHが低いと耐光性付与効
果が不十分であり、また高いと該充填剤を配合し
た組成物は増粘ゲル化し易くなる。かかる観点か
ら例えば炭酸カルシウムの単独または炭酸カルシ
ウムと水酸化アルミニウムとの併用が好ましい。
本発明のバツキング組成物は、基本的にはビニ
ルエステル―エチレン―塩化ビニル系共重合体エ
マルジヨンと塩基性無機質充填剤から構成される
が、それぞれの使用目的条件に応じて更に難燃剤
を加える事ができる。
例えば、難燃剤としてはリン酸エステル系化合
物、含ハロゲンリン酸エステル系化合物、ポリリ
ン酸アンモニウム、三酸化アンチモン、ホウ酸亜
鉛、メタホウ酸バリウムなど従来より公知のもの
で何ら差しつかえない。また、難燃剤の他の公知
の増粘剤、分散剤、着色剤などを必要に応じて適
宜配合しても良い。
また、本発明で用いられるビニルエステル―エ
チレン―塩化ビニル系共重合体エマルジヨンは従
来一般に用いられてきたスチレン―ブタジエン共
重合体ラテツクスあるいは酢酸ビニル―エチレン
共重合体エマルジヨンなどとブレンドして用いて
もよい。
本発明のバツキング組成物を用いる敷物の繊維
素材としては、レーヨン、羊毛、ナイロン、ポリ
プロピレン、ポリエステル、ポリアクリロニトリ
ルなど天然もしくは合成繊維を問わず用いる事が
できる。敷物の編織組織にとくに限定はなく、一
般にタフテツドカーペツト、ニードルパンチカー
ペツトや自動車座席シート用にも用いる事ができ
る。
本発明のバツキング組成物を敷物に塗布する方
法としては、ロールコーター、フローコーター、
スプレーなど公知の装置でよく、塗布後熱風、赤
外線などにより乾燥される。しかるのち、自動車
用カーペツトではポリエチレンのホツトメルトコ
ーテイングとフエルトとの一体化成型なども行わ
れる事もある。塗布量としては、特に制限はない
が、安定した結果を得るためには固形分として1
m3当り0.1〜2.0Kgが適当である。また、必要に応
じて該バツキング組成物を適度に発泡させてのち
塗布する事もできる。かくして得られた敷物は十
分にすぐれた難燃性、耐水性、抜糸強度、形状安
定性および耐水性を有するものである。
以下に本発明を実施例により説明する。
実施例1〜9および比較例1〜6
主成分であるバインダーとして酢酸ビニル―エ
チレン―塩化ビニル系共重合体エマルジヨンを用
い、第一表および第二表に示すような配合処方に
てそれぞれバツキング組成物を作成した。
前記実施例1〜9および比較例1〜6で得たバ
ツキング組成物をポリプロピレン繊維100%の目
付量約560g/m3のニードルパンチカーペツトの
裏面に転写方式にて固形分として150g/m3にな
るように塗布し、110℃×20分乾燥を行なう。こ
のバツキング物を所定の寸法に裁断し、バツキン
グ面に約10mm厚のフエルトを当て、高温型紫外線
フエードメーター(スガ試験機KK)で83℃±3
℃にて300時間の紫外線照射を行ないカーペツト
の照射面のポリプロピレン繊維の熱劣化、形態く
ずれおよび変退色を調べた。その結果は第一表お
よび第二表にそれぞれ付す。
(耐光性試験評価法)
○ :カーペツト表面の繊維劣化、形くずれお
よび変退色はなし。
○―△:繊維の劣化がわずかに認められる。変退
色はなし。
△ :繊維の劣化、形くずれがかなり認められ
る。変退色なし。
:繊維劣化が激しく形くずれがかなり認め
られる。変退色なし。
The present invention relates to a composition for backing rugs.
More specifically, the present invention relates to a backing composition for rugs comprising an emulsion containing a vinyl ester-ethylene-vinyl chloride copolymer and a basic inorganic filler. Traditionally, carpets with various textures and structures have been used, and in recent years, carpets with piles embedded in the base fabric called tufted carpets and webs have been used for reasons such as simplicity and economy in the manufacturing process. Needle punch carpets that are mechanically entangled using the needle punching method are often used. Such rugs have piles or webs that are merely mechanically intertwined, so the shape is unstable and cannot be put to practical use as is. Therefore, natural rubber, synthetic rubber latex, or synthetic resin emulsion is usually applied to the front or back surface of the rug, either alone or in the form of a mixture, and then dried to give the rug strength and dimensional stability. These rugs are used for a variety of purposes, including homes, vehicles, aircraft, and ships, but in recent years, flame-retardant regulations have been tightened for such rugs to prevent fire accidents. For this reason, various methods are being considered, such as making the fiber itself flame retardant and making it flame retardant with a backing agent, but flame retardant using a backing agent is currently the mainstream from the economical and technical aspects. . Among these uses, flame retardant regulations have been applied to carpets, which have been recently installed as materials for vehicles, especially for the interior of automobiles, and in addition, standards for heat and light resistance have recently been further strengthened, making them particularly difficult to use. In addition to flammability, it is also necessary to address heat and light resistance. The fibers used to make needle punch carpets, which are often used for automobile interiors, have traditionally been a blend of vinyl chloride, vinylidene chloride fibers, and other fibers, but due to the need to reduce weight, The reason for the switch to polypropylene fibers is that polypropylene is a highly combustible material, and in response to the need for increased flame retardancy in these fields, performance improvements with backing agents are required more than ever before. It's summery. For this reason, in the conventional synthetic rubber latex used as a backing agent, such as styrene-butadiene copolymer latex, it is necessary to increase the amount of flame retardant added, but even though this method is effective for flame retardation, it inherently causes backing. The disadvantage is that the reinforcing effect is significantly impaired in terms of stabilizing the shape of the pile to prevent thread removal, which is the purpose of this method. Under these circumstances, beer ester-ethylene-vinyl chloride copolymer emulsions have recently been increasingly used in place of conventional synthetic rubber latexes. Vinyl ester-ethylene-vinyl chloride copolymer emulsion has many halogens in its molecules, and especially when a copolymer with a high halogen content is used as a backing agent, the copolymer itself is self-extinguishing. Therefore, it is easy to make flame retardant with a backing agent, and the purpose can be achieved even with a small amount of flame retardant. It is possible to not only provide the original suture removal strength and maintain stable shape, but also provide excellent water resistance due to the fact that the copolymer is a hydrophobic polymer. Furthermore, among the necessary performances for automobile rugs, good performance is required not only in terms of flame retardancy, thread removal strength, shape stability, and water resistance, but also in terms of light resistance. For example, there is a need for a backing agent that does not cause deterioration in performance, such as loss of shape due to a decrease in the strength of the rug, especially when exposed to axial heat or light from the sun through window glass. Therefore, in recent years, the test standards have been strengthened to test under even more severe conditions than the conventional test method using an ultraviolet fade meter to accelerate the light resistance of the rug. For example, the temperature conditions for testing have become stricter, increasing from 63°C to 83°C. Even in this strict test standard, a backing agent that does not cause deterioration, loss of shape, discoloration or fading of the fibers of the rug itself is required. For these reasons, the present inventors have conducted various studies to further improve the light resistance of the vinyl ester-ethylene-vinyl chloride copolymer without impairing its original performance for rugs. By adding , flame retardancy, suture removal strength,
The present inventors have discovered a backing composition that maintains properties such as shape stability and water resistance, and has significantly superior light resistance, thereby completing the present invention. That is, the present invention comprises a vinyl ester-ethylene-vinyl chloride copolymer emulsion and a basic inorganic filler as essential components, and if necessary, a flame retardant,
The present invention provides a composition for backing a rug, which has excellent light resistance and is blended with a dispersant, a thickener, and the like. The main binder used in the bucking composition of the present invention is a vinyl ester-ethylene-vinyl chloride copolymer emulsion, and the constituent monomer composition ratio of the copolymer is vinyl ester: ethylene: vinyl chloride = 10 to 55. :5-30:30-75 weight ratio. The vinyl ester is preferably vinyl acetate. Vinyl esters include vinyl propionate and vinyl versatate. Furthermore, part of the vinyl ester may be replaced with an acrylic ester or a methacrylic ester, and the vinyl ester may be used in combination with vinyl acetate, particularly preferably. Additionally, a small amount of a functional vinyl monomer such as (meth)acrylic acid, maleic acid monoester, N-methylol acrylamide, N-butoxymethyl acrylamide, acrylamide, glycidyl methacrylate, or hydroxyethyl acrylate is copolymerized with the copolymer. A copolymer emulsion may also be used. All of these copolymer emulsions can be obtained by conventional emulsion manufacturing methods. Basic inorganic fillers used in the present invention include metal oxides, hydroxides, and carbonates such as calcium carbonate, aluminum hydroxide, magnesium oxide, talc, zinc white, and calcium hydroxide, which are commonly commercially available. The amount used is 30 to 160 parts by weight, preferably 60 to 100 parts by weight, based on 100 parts by weight of the solid content of the vinyl ester-ethylene-vinyl chloride copolymer emulsion. The basic inorganic filler may be used alone or in combination of two or more. In this case, if the amount of the basic inorganic filler used is less than the above range, it will be difficult to obtain excellent light resistance, and if it is more than the above range, the physical strength will decrease. The emulsion used in the backing composition is required to be stable so that it will not thicken or coagulate when a basic substance is added. Therefore, it is necessary to sufficiently impart the above-mentioned properties, particularly light resistance, to the carpet obtained by backing, maintain the stability of the copolymer emulsion, and balance the performance and workability of the backing composition. For this reason, the basic inorganic filler used in the present invention is specifically prepared by dispersing 10 g of the filler in 40 g of ion-exchanged water, and the pH of the supernatant is 8 to 9.
It is preferable to have a medium basicity within the range of 10 to 10. In this case, if the PH is low, the effect of imparting light resistance will be insufficient, and if it is high, the composition containing the filler will thicken and gel. It becomes easier. From this point of view, it is preferable to use calcium carbonate alone or in combination with calcium carbonate and aluminum hydroxide. The bucking composition of the present invention basically consists of a vinyl ester-ethylene-vinyl chloride copolymer emulsion and a basic inorganic filler, but a flame retardant may be added depending on the intended use conditions. I can do it. For example, as the flame retardant, conventionally known flame retardants such as phosphoric acid ester compounds, halogen-containing phosphoric acid ester compounds, ammonium polyphosphate, antimony trioxide, zinc borate, barium metaborate, etc. may be used. In addition, other known thickeners, dispersants, colorants, etc. other than flame retardants may be appropriately blended as necessary. Furthermore, the vinyl ester-ethylene-vinyl chloride copolymer emulsion used in the present invention may be blended with conventionally commonly used styrene-butadiene copolymer latex or vinyl acetate-ethylene copolymer emulsion. good. As the fiber material for the rug using the bucking composition of the present invention, natural or synthetic fibers such as rayon, wool, nylon, polypropylene, polyester, and polyacrylonitrile can be used. There are no particular restrictions on the weaving structure of the rug, and it can generally be used for tufted carpets, needle punch carpets, and automobile seats. Methods for applying the bucking composition of the present invention to a rug include a roll coater, a flow coater,
A known device such as a sprayer may be used, and after application, it is dried using hot air, infrared rays, etc. Later, in automobile carpets, polyethylene hot melt coating and felt were sometimes integrally molded. There is no particular limit to the amount of application, but in order to obtain stable results, the solid content should be 1.
0.1 to 2.0 kg per m 3 is suitable. Further, if necessary, the backing composition can be foamed appropriately and then applied. The thus obtained rug has sufficiently excellent flame retardancy, water resistance, suture removal strength, shape stability, and water resistance. The present invention will be explained below using examples. Examples 1 to 9 and Comparative Examples 1 to 6 Vinyl acetate-ethylene-vinyl chloride copolymer emulsion was used as the main binder, and packing compositions were prepared using the formulations shown in Tables 1 and 2, respectively. created something. The backing compositions obtained in Examples 1 to 9 and Comparative Examples 1 to 6 were transferred onto the back side of a needle punch carpet made of 100% polypropylene fibers with a basis weight of approximately 560 g/m 3 as a solid content of 150 g/m 3 . Apply it so that it looks like this and dry it for 20 minutes at 110℃. Cut this bucking material to the specified size, apply approximately 10 mm thick felt to the buckling surface, and use a high-temperature ultraviolet fade meter (Suga Test Instruments KK) to 83℃±3.
The polypropylene fibers on the irradiated surface of the carpet were irradiated with ultraviolet rays at ℃ for 300 hours, and thermal deterioration, deformation, and discoloration were investigated. The results are shown in Tables 1 and 2, respectively. (Lightfastness test evaluation method) ○: No fiber deterioration, deformation, discoloration or fading on the carpet surface. ○-△: Slight deterioration of fibers is observed. No discoloration or fading. △: Significant deterioration and deformation of fibers are observed. No discoloration or fading. : Severe fiber deterioration and considerable deformation observed. No discoloration or fading.
【表】【table】
【表】【table】
Claims (1)
重合体エマルジヨンの固形分100重量部に対し塩
基性無機充填剤30〜160重量部を配合してなり、
かつ当該ビニルエステル―エチレン―塩化ビニル
系共重合体エマルジヨンの組成が、ビニルエステ
ル10〜55重量%、エチレン5〜30重量%、塩化ビ
ニル30〜75重量%であり、 当該塩基性無機充填剤が該充填剤の10gを40g
のイオン交換水にて分散せしめた上澄液のPHが8
〜9であることを特徴とする敷物バツキング用組
成物。[Claims] 1. 30 to 160 parts by weight of a basic inorganic filler is blended with 100 parts by weight of the solid content of a vinyl ester-ethylene-vinyl chloride copolymer emulsion,
and the composition of the vinyl ester-ethylene-vinyl chloride copolymer emulsion is 10 to 55% by weight of vinyl ester, 5 to 30% by weight of ethylene, and 30 to 75% by weight of vinyl chloride, and the basic inorganic filler is 10g of the filler to 40g
The pH of the supernatant liquid dispersed in ion-exchanged water is 8.
9. A composition for rug bucking, characterized in that the composition is
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14902480A JPS5773037A (en) | 1980-10-23 | 1980-10-23 | Carpet-backing composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14902480A JPS5773037A (en) | 1980-10-23 | 1980-10-23 | Carpet-backing composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5773037A JPS5773037A (en) | 1982-05-07 |
JPS649341B2 true JPS649341B2 (en) | 1989-02-17 |
Family
ID=15465995
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14902480A Granted JPS5773037A (en) | 1980-10-23 | 1980-10-23 | Carpet-backing composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5773037A (en) |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5229340B2 (en) * | 1971-11-09 | 1977-08-01 | ||
JPS5023853B2 (en) * | 1972-04-10 | 1975-08-11 |
-
1980
- 1980-10-23 JP JP14902480A patent/JPS5773037A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5773037A (en) | 1982-05-07 |
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