JPH0635571B2 - Adhesive composition for car backpacking - Google Patents
Adhesive composition for car backpackingInfo
- Publication number
- JPH0635571B2 JPH0635571B2 JP11264485A JP11264485A JPH0635571B2 JP H0635571 B2 JPH0635571 B2 JP H0635571B2 JP 11264485 A JP11264485 A JP 11264485A JP 11264485 A JP11264485 A JP 11264485A JP H0635571 B2 JPH0635571 B2 JP H0635571B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- adhesive composition
- parts
- adhesive
- carpet
- 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 - Lifetime
Links
- 239000000853 adhesive Substances 0.000 title claims description 51
- 230000001070 adhesive effect Effects 0.000 title claims description 51
- 239000000203 mixture Substances 0.000 title claims description 39
- 239000000178 monomer Substances 0.000 claims description 26
- 229920001577 copolymer Polymers 0.000 claims description 15
- 229920000126 latex Polymers 0.000 claims description 13
- 239000004816 latex Substances 0.000 claims description 13
- 239000000945 filler Substances 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 8
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- 150000001993 dienes Chemical class 0.000 claims description 7
- 150000005673 monoalkenes Chemical class 0.000 claims description 5
- 229920001296 polysiloxane Polymers 0.000 claims description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- 238000000034 method Methods 0.000 description 12
- -1 defoamers Substances 0.000 description 9
- 239000004743 Polypropylene Substances 0.000 description 8
- 229920001155 polypropylene Polymers 0.000 description 8
- 244000025254 Cannabis sativa Species 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- 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
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000002313 adhesive film Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- TWYSBDNLTRUTQT-UHFFFAOYSA-A hexadecapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O TWYSBDNLTRUTQT-UHFFFAOYSA-A 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-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
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 206010057040 Temperature intolerance Diseases 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 230000008543 heat sensitivity Effects 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
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
【発明の詳細な説明】 イ.発明の目的 〔産業上の利用分野〕 本発明は、タフテッド・カーペット、人工芝などのカー
ペットの製造時に使用される接着剤組成物を提供するも
のである。Detailed Description of the Invention a. OBJECT OF THE INVENTION [Industrial field of application] The present invention provides an adhesive composition used in the production of carpets such as tufted carpets and artificial turf.
従来、広く製造されているタフテッドカーペットでは、
主にパイル(ふさ糸)の脱落を防ぐために合成ゴムラテ
ックスを主剤とする接着剤組成物が使用されている。Traditionally, widely manufactured tufted carpets,
An adhesive composition containing a synthetic rubber latex as a main component is mainly used to prevent the pile (braided yarn) from falling off.
この接着剤組成物は、裏張り材の接着、ほつれ防止なら
びに好ましい風合および寸法安定性の付与などの役割も
はたしている。The adhesive composition also plays a role of adhering the backing material, preventing fraying, and imparting favorable feeling and dimensional stability.
さらに、溶剤系接着剤と比較してラテックス接着剤組成
物は、 カーペット加工時に火災の危険性がない、 高固形分の接着剤組成物が得られる、 有機溶剤による公害がない、 パイル中への接着剤組成物の浸透が適当である、 などの実用上種々の長所がある。In addition, the latex adhesive composition, compared to solvent-based adhesives, has no fire hazard during carpet processing, high solids adhesive composition can be obtained, no pollution by organic solvent, There are various practical advantages such as proper penetration of the adhesive composition.
しかし、ラテックス接着剤は、潜熱の大きい水を蒸発さ
せる必要があり、このために大量のエネルギーを消費す
るという問題点がある。However, the latex adhesive has a problem in that it needs to evaporate water having a large latent heat, which consumes a large amount of energy.
一方、カーペットの製造工程では、生産性を高めるた
め、大型の乾燥機を使用し高温による乾燥が行われてい
る。この様に、高温乾燥を実施すると接着剤組成物の内
部にて沸騰がおき、接着剤皮膜が部分的にカーペットの
裏面に吹き出して、カーペットの商品価値を著しく損う
ことがある。On the other hand, in the carpet manufacturing process, in order to improve productivity, a large dryer is used to perform drying at a high temperature. As described above, when high-temperature drying is carried out, boiling occurs inside the adhesive composition, and the adhesive film partially blows out on the back surface of the carpet, which may significantly impair the commercial value of the carpet.
この現象はブリスターと呼ばれており、ラテックス接着
剤を用いるカーペットの製造工程では生産性の向上に大
きな障害となっている。This phenomenon is called a blister and is a major obstacle to improving productivity in the carpet manufacturing process using a latex adhesive.
また、通常のカーペットは屋内で使用されることが多い
が、人工芝のように屋外で使用されるものもある。加え
て、屋外にて使用されるカーペットでは高度の耐水性が
必要とされる。しかしながら、屋内にて使用されるカー
ペットにおいても洗濯もしくはクリーニングされるもの
があり、耐水性の向上が望まれている。In addition, ordinary carpets are often used indoors, but there are also carpets that are used outdoors such as artificial grass. In addition, carpets used outdoors require a high degree of water resistance. However, some carpets used indoors are also washed or cleaned, and improvement in water resistance is desired.
カーペットの製造工程におけるブリスターを抑制する方
法として、従来技術では、特公昭59第47754号、
特許第1099716号および特公昭56第44191
号公報において、接着剤組成物に含まれる充填剤の粒子
径と添加量を選択することにより接着剤皮膜の透気度を
向上させる方法、および接着剤にあらかじめ感熱剤を添
加して乾燥中に接着剤を早く凝固させることによりブリ
スターの発生を抑える方法が提案されている。As a method for suppressing blisters in the carpet manufacturing process, in the prior art, Japanese Patent Publication No. 47754 /
Japanese Patent No. 1099716 and Japanese Examined Patent Publication No. 5644191
In the publication, a method for improving the air permeability of the adhesive film by selecting the particle size and the addition amount of the filler contained in the adhesive composition, and adding a heat sensitive agent in advance to the adhesive during drying. A method has been proposed in which the occurrence of blisters is suppressed by rapidly solidifying the adhesive.
また、ラテックス接着剤の耐水性を向上させる方法とし
ては、接着剤中に含まれる水溶性物質、とりわけ界面活
性剤を可能な限り減らすこと、および架橋剤を使用する
ことなどの方法が行われている。Further, as a method of improving the water resistance of the latex adhesive, a method such as reducing the water-soluble substance contained in the adhesive, especially a surfactant as much as possible, and using a crosslinking agent is performed. There is.
従来の技術の項でも述べたように、ブリスターの防止に
は充填剤による方法と感熱剤による方法がある。As described in the section of the prior art, there are a method using a filler and a method using a heat sensitive agent for preventing blisters.
充填剤による方法は、充填剤量の多い接着剤の場合には
有効であるが、高い接着力および優れた耐水性が必要と
される場合には充填剤量を減少させねばならず充分な耐
ブリスター性を得ることが困難となる。The method using a filler is effective in the case of an adhesive having a large amount of filler, but when high adhesive strength and excellent water resistance are required, the amount of the filler must be reduced and sufficient resistance is required. It becomes difficult to obtain the blister property.
感熱剤による方法においても、接着剤組成物が熱に対し
て不安定となるのみならず、接着剤組成物作成時の撹拌
安定性、接着剤組成物の機械的安定性、貯蔵時の粘度安
定性などが低下する欠点がある。この改良には、乳化剤
が併用される。一般には、感熱性を損わないために曇点
を有するノニオン系界面活性剤が併用される。Even in the method using a heat sensitive agent, not only the adhesive composition becomes unstable to heat, but also the stirring stability during the preparation of the adhesive composition, the mechanical stability of the adhesive composition, and the viscosity stability during storage. There is a drawback that it deteriorates the sex. An emulsifier is used in combination for this improvement. Generally, a nonionic surfactant having a cloud point is used together so as not to impair the heat sensitivity.
前述の特公昭59−47754号、特許第109971
6号および特公昭56− 44191号の技術も、この問題の
解決のためにノニオン系界面活性剤を使用している。The aforementioned Japanese Patent Publication No. 59-47754 and Japanese Patent No. 109971.
The techniques of No. 6 and Japanese Patent Publication No. 56-44191 also use nonionic surfactants to solve this problem.
ところが、このようなノニオン系界面活性剤の使用は、
接着剤組成物の耐水性を低下させるという根本的な問題
があり、耐ブリスター性と耐水性の両者を同時に満足さ
せることは困難であったことから、改良が望まれてい
た。However, the use of such a nonionic surfactant is
There is a fundamental problem of reducing the water resistance of the adhesive composition, and it is difficult to satisfy both the blister resistance and the water resistance at the same time, and therefore, improvement has been desired.
本発明者らは、上記問題点に鑑み、耐水性、とりわけ耐
水接着力に優れ、ブリスターの少ないカーペット用接着
剤組成物の開発を目的とし研究を重ねた結果、本発明を
完成した。In view of the above problems, the present inventors have completed the present invention as a result of repeated research aiming at development of an adhesive composition for carpet which is excellent in water resistance, particularly in water resistance, and has less blisters.
ロ.発明の構成 〔本発明の構成〕 本発明は、脂肪族共役ジエン系単量体35〜80重量
%、エチレン系不飽和カルボン酸0.5〜4.0重量%
およびこれらの共重合可能なモノオレフィン系単量体1
6.0〜64.5重量%を乳化重合し得られた共重合体
の存在下、脂肪族共役ジエン系単量体0〜20重量%お
よびモノオレフィン系単量体80〜100重量%を添加
し重合させた共重合体ラテックス100重量部(固形
分)に対し、オルガノポリシロキサン0.01〜3重量
部および充填剤0〜600重量部を含有することを特徴
とするカーペットバッキング用接着剤組成物を提供する
ものである。以下に、本発明をさらに詳しく説明する。B. Structure of the Invention [Structure of the Invention] The invention comprises 35 to 80% by weight of an aliphatic conjugated diene monomer and 0.5 to 4.0% by weight of an ethylenically unsaturated carboxylic acid.
And their copolymerizable mono-olefin monomers 1
In the presence of a copolymer obtained by emulsion polymerization of 6.0 to 64.5% by weight, 0 to 20% by weight of an aliphatic conjugated diene monomer and 80 to 100% by weight of a monoolefin monomer are added. Adhesive composition for carpet backing, characterized by containing 0.01 to 3 parts by weight of organopolysiloxane and 0 to 600 parts by weight of filler with respect to 100 parts by weight (solid content) of the polymerized copolymer latex. It is to provide things. The present invention will be described in more detail below.
初期に共重合させる単量体のうち、脂肪族共役ジエン系
単量体は、35〜80重量%で用いられるが、35重量
%未満では得られる共重合体の二次転移温度が高くカー
ペットに用いた場合に適当な風合が得られない。また、
80重量%を越えると接着力が低下する。Among the monomers to be initially copolymerized, the aliphatic conjugated diene-based monomer is used in an amount of 35 to 80% by weight, but if it is less than 35% by weight, the resulting copolymer has a high second-order transition temperature and is used in carpets. When used, it does not give a suitable texture. Also,
If it exceeds 80% by weight, the adhesive strength will decrease.
本発明にて使用される脂肪族共役ジエン系単量体として
は、1,3−ブタジエン、イソプレン、2−クロル1,
3−ブタジエンなどがあげられる。本発明にて使用され
るエチレン系不飽和カルボン酸は、0.5〜4.0重量
%で用いられるが、0.5重量%未満では接着強度が低
下し、かつ接着剤組成物の機械的安定性も低下する。ま
た、4.0重量%を越えると接着剤組成物の耐ブリスタ
ー性が悪化するばかりでなく、耐水性も低下する。本発
明にて用いるエチレン系不飽和カルボン酸としては、マ
レイン酸、フマール酸、イタコン酸、アクリル酸、メタ
クリル酸などがあげられる。また、これらのうち、1種
または2種以上を併用して使用することができる。Examples of the aliphatic conjugated diene-based monomer used in the present invention include 1,3-butadiene, isoprene, 2-chloro-1,
3-butadiene etc. are mentioned. The ethylenically unsaturated carboxylic acid used in the present invention is used in an amount of 0.5 to 4.0% by weight, but if it is less than 0.5% by weight, the adhesive strength decreases and the mechanical strength of the adhesive composition is reduced. Stability is also reduced. Further, if it exceeds 4.0% by weight, not only the blister resistance of the adhesive composition is deteriorated but also the water resistance is deteriorated. Examples of the ethylenically unsaturated carboxylic acid used in the present invention include maleic acid, fumaric acid, itaconic acid, acrylic acid and methacrylic acid. Further, of these, one kind or two or more kinds can be used in combination.
本発明にて使用されるモノオレフィン系単量体として
は、スチレン、α−メチルスチレン、アクリロニトリ
ル、メチルメタクリレート、β−ヒドロキシエチルアク
リレートなどがあげられる。これらモノオレフィン系単
量体は、1種もしくは2種以上を併用して使用すること
ができるが、とりわけスチレンが好ましい。Examples of the monoolefin-based monomer used in the present invention include styrene, α-methylstyrene, acrylonitrile, methyl methacrylate, β-hydroxyethyl acrylate and the like. These mono-olefin monomers can be used alone or in combination of two or more, and styrene is particularly preferable.
本発明にて初期に共重合させる単量体の量は、得られる
カーペットの低温時の風合および接着力の点で、全体の
単量体の60〜90重量%で用いるのが好ましい。The amount of the monomer to be initially copolymerized in the present invention is preferably 60 to 90% by weight based on the total amount of the monomers in terms of the feel and adhesive strength of the resulting carpet at low temperature.
次いで、後期に共重合される単量体のうち脂肪族共役ジ
エン系単量体は、0〜20重量%で用いられるが、20
重量%を越えると接着力が低下する。単量体の添加方法
は、連続、分割、一括添加方法のいずれでも良く、特に
限定はない。Then, the aliphatic conjugated diene-based monomer is used in an amount of 0 to 20% by weight among the monomers copolymerized in the latter stage.
If the content exceeds 50% by weight, the adhesive strength will decrease. The method of adding the monomer may be any of continuous, divided, and batch addition methods and is not particularly limited.
さらに、初期に共重合させる単量体の重合転化率が70
重量%以上になったとき、後期に共重合させる単量体を
添加するのが好ましい。Further, the polymerization conversion rate of the monomer to be copolymerized in the initial stage is 70
It is preferable to add a monomer to be copolymerized at a later stage when the amount is at least wt%.
本発明で使用されるオルガノポリシロキサンは、特公昭
40−21427号、特公昭47−19064号、米国
特許第3246339号、同第325514号および英
国特許第1141867号公報明細書に記載されているものを
例示できる。The organopolysiloxane used in the present invention is described in JP-B-40-21427, JP-B-47-19064, US Pat. Nos. 3,246,339, 325514 and British Patent No. 1141867. Can be illustrated.
本発明にて用いるオルガノポリシロキサンは、0.01
〜3重量部で使用されるが、0.01重量部未満ではブ
リスターを防止する効果が不十分であり、3重量部を越
えると接着剤組成物の貯蔵時の粘度変化が大きくなり、
実用上問題がある。The organopolysiloxane used in the present invention is 0.01
It is used in an amount of up to 3 parts by weight, but if it is less than 0.01 parts by weight, the effect of preventing blisters is insufficient, and if it exceeds 3 parts by weight, the viscosity change of the adhesive composition during storage becomes large,
There are practical problems.
本発明にて使用される充填剤としては、炭酸カルシウ
ム、水酸化アルミニウム、シリカ、クレーなどがあげら
れ、これらは1種もしくは2種以上を併用して使用する
ことができる。Examples of the filler used in the present invention include calcium carbonate, aluminum hydroxide, silica, clay and the like, and these can be used alone or in combination of two or more.
本発明にて用いる充填剤は、共重合体ラテックス固形分
100重量部当り、600重量部以下で使用される。充
填剤量が600重量部を越えると、得られるカーペット
の接着力および耐水性が低下して好ましくない。充填剤
量は、カーペットの接着力および耐水性の面から100
〜400重量部であることが更に好ましい。The filler used in the present invention is used in an amount of 600 parts by weight or less per 100 parts by weight of the solid content of the copolymer latex. When the amount of the filler exceeds 600 parts by weight, the adhesive strength and water resistance of the resulting carpet are deteriorated, which is not preferable. The amount of the filler is 100 in terms of the adhesive strength and water resistance of the carpet.
More preferably, the amount is 400 parts by weight.
本発明の接着剤組成物には、一般に添加されている老化
防止剤、分散剤、消泡剤、増粘剤、着色剤、架橋剤、架
橋助剤等が使用できる。In the adhesive composition of the present invention, generally added antioxidants, dispersants, defoamers, thickeners, colorants, crosslinking agents, crosslinking aids and the like can be used.
以下に実施例をあげて本発明を詳細に説明するが、本発
明は実施例によって何ら限定されるものではない。Hereinafter, the present invention will be described in detail with reference to examples, but the present invention is not limited to the examples.
なお、実施例中に使用される部数および%は、ことわり
のない限りすべて重量部および重量%を意味する。All parts and% used in the examples mean parts by weight and% by weight unless otherwise specified.
実施例−1 (1) 共重合体ラテックスの重合 撹拌機を備えた耐圧容器に、表−1に示した初期単量
体、アルキルベンゼンスルホン酸ナトリウム1.0部、
炭酸水素ナトリウム0.6部、過硫酸カリウム0.8
部、tert.−ドデシルメルカプタン0.5部、水100
部およびエチレンジアミン四酢酸ナトリウム0.05部
を仕込み、70℃にて重合転化率が80%を越えるまで
重合させた。Example-1 (1) Polymerization of copolymer latex In a pressure vessel equipped with a stirrer, the initial monomers shown in Table-1, sodium alkylbenzenesulfonate 1.0 part,
Sodium hydrogen carbonate 0.6 part, potassium persulfate 0.8
Part, tert. -0.5 parts dodecyl mercaptan, 100 water
Parts and 0.05 parts of sodium ethylenediaminetetraacetate were charged and polymerized at 70 ° C. until the polymerization conversion rate exceeded 80%.
次いで、第1表に示す後期に共重合させる単量体を添加
し、70℃にて重合を行い、共重合体ラテックス1〜3
を得た。Then, the monomers to be copolymerized at the latter stage shown in Table 1 are added and polymerized at 70 ° C. to obtain copolymer latexes 1 to 3.
Got
同様にして、比較例として表−1に示す初期および後期
単量体にて重合を行い、共重合体ラテックス4および5
を得た。In the same manner, as a comparative example, polymerization was performed using the initial and late monomers shown in Table 1 to obtain copolymer latexes 4 and 5
Got
これら共重合体ラテックスの重合転化率は、いずれも9
7%以上であった。未反応単量体を減圧下の水蒸気蒸留
により除去したのち、水酸化ナトリウム水溶液によりP
Hを8.0〜8.5に調整した。The polymerization conversion rate of these copolymer latexes is 9 in each case.
It was 7% or more. Unreacted monomer is removed by steam distillation under reduced pressure, and then P is washed with an aqueous solution of sodium hydroxide.
The H was adjusted to 8.0 to 8.5.
(2) 接着剤組成物の作成 (1)で得られた共重合体ラテックスを用いて下記の配合
処方に従い総固形分80%、粘度20000センチポイ
ズの接着剤組成物A〜DおよびE〜Jを作成した。 (2) Preparation of adhesive composition Using the copolymer latex obtained in (1), adhesive compositions A to D and E to J having a total solid content of 80% and a viscosity of 20,000 centipoise were prepared according to the following formulation. Created.
配合処方(固形分,部) 共重合体ラテックス 100 テトラピロリン酸カリウム 1 フェノール系酸化防止剤 0.5 増 粘 剤 必要量 水 必要量 (3) タフテッドカーペットの作成 (2)で得られた接着剤組成物を基布がポリプロピレンス
プリットヤーン、パイルがナイロンのタフテッドカーペ
ット生機の裏面に1m2当り見掛重量1100gを均一に
塗布し、ポリプロピレン織布を貼り合せた。Formulation (solid content, parts) Copolymer latex 100 Potassium tetrapyrophosphate 1 Phenolic antioxidant 0.5 Thickening agents necessary amount water necessary amount (3) viewed 1 m 2 per a back surface of the tufted carpet create the base fabric of polypropylene split yarn and the resulting adhesive composition (2), the pile tufted carpet greige nylon A hanging weight of 1100 g was evenly applied, and a polypropylene woven fabric was attached.
130℃のオーブンにて15分間乾燥し、タフテッドカ
ーペットを作成した。A tufted carpet was prepared by drying in an oven at 130 ° C for 15 minutes.
(4) 物性の測定 (a) 接着剤組成物の貯蔵時の粘度安定性 (2)で得られた接着剤組成物を40℃で14日間放置
後、25℃まで放冷し、粘度を測定した。(B型粘度
計、4号ローター使用。回転数12 rpm) (b) 接着剤組成物のマロン式機械的安定性 JISK−6392に準拠し、(2)で得られた接着剤組
成物の見掛重量50gを荷重10kg、回転数1000 r
pmで10分間撹拌した。その後、100メッシュ金網で
過、水洗した後に乾燥・放冷し、発生する凝集物の重
量を%で表示した。(4) Measurement of physical properties (a) Stability of viscosity of adhesive composition during storage (2) The adhesive composition obtained in (2) was left at 40 ° C for 14 days, then allowed to cool to 25 ° C and the viscosity was measured. did. (B-type viscometer, No. 4 rotor used, rotation speed 12 rpm) (b) Marron mechanical stability of the adhesive composition According to JISK-6392, the adhesive composition obtained in (2) was observed. Hanging weight 50g, load 10kg, rotation speed 1000r
Stirred at pm for 10 minutes. Then, after passing through a 100-mesh wire net, washing with water, drying and cooling, the weight of aggregates generated was expressed in%.
(c) ブリスター特性 (2)で得られた接着剤組成物を基布がポリプロピレン・
スプリットヤーン、パイルがナイロンのタフテッドカー
ペット生機の裏面に見掛重量1500g/m2にて均一に
塗布し、ポリプロピレン織布の裏張り材をこの上に貼付
して未乾燥のカーペットを得た。(c) The adhesive composition obtained in the blister property (2) is made of polypropylene
A tufted carpet made of nylon with split yarns and piles was evenly applied on the back side of a greige machine at an apparent weight of 1500 g / m 2 , and a lining material of polypropylene woven cloth was stuck on this to obtain an undried carpet.
未乾燥カーペットを温度170℃、熱風速度20m/秒
の乾燥機にて3分間乾燥させ、発生したブリスターを肉
眼にて観察し、下記の級別にて判定した。The undried carpet was dried for 3 minutes in a dryer at a temperature of 170 ° C. and a hot air speed of 20 m / sec, and the generated blister was visually observed and judged according to the following grades.
1級:ブリスターの発生が全く認められない。Grade 1: No blister is observed.
8級:ブリスターが全面に多く発生している。 Grade 8: Many blisters occur on the entire surface.
(d) 裏張り材のはく離強度およびパイル糸の引抜き強
度 (3)で得られたカーペットをJISL−1021「敷物試験
方法」に準拠し、裏張り材のはく離強度およびパイル糸
の引抜き強度を測定した。(d) Peeling strength of backing material and pull-out strength of pile yarn The carpet obtained in (3) was measured for peeling strength of the backing material and pull-out strength of pile yarn according to JIS L-1021 "Rug Test Method". did.
(e) 耐水強度 (3)で得られたカーペットを60℃の温水に120分間
浸漬した後、ゆるく脱水し、(d)と同様に裏張り材のは
く離強度を測定した。(e) Water resistance The carpet obtained in (3) was immersed in warm water at 60 ° C. for 120 minutes and then gently dehydrated, and the peel strength of the backing material was measured in the same manner as in (d).
(a)〜(e)の結果を表−2に示した。The results of (a) to (e) are shown in Table-2.
実施例−2 (1) 人工芝用接着剤組成物の作成 実施例−1で重合した共重合体ラテックス2ならびに4
を下記の処方に従い、総固形分70%、粘度10000
センチポイズの人工芝用接着剤組成物K〜Rを作成し
た。 Example-2 (1) Preparation of adhesive composition for artificial turf Copolymer latex 2 and 4 polymerized in Example-1
According to the following formulation, total solid content 70%, viscosity 10000
Centipoise artificial turf adhesive compositions KR were prepared.
配合処方(固形分,部) 共重合体ラテックス 100 テトラピロリン酸カリウム 0.5 フェノール系酸化防止剤 0.8 硫 黄 1.0 ソクシノール BZ 1.0 〃 MZ 1.0 増 粘 剤 必要量 水 必要量 (2) 人工芝の作成 (1)で得られた接着剤組成物を、基布がポリプロピレン
スプリットヤーン、パイルもポリプロピレンの人工芝生
機の裏面に1m2当り見掛重量600gを均一に塗布し、
120℃のオーブンにて20分乾燥し、人工芝を作成し
た。Formulation (solid content, parts) Copolymer latex 100 Potassium tetrapyrophosphate 0.5 Phenolic antioxidant 0.8 Sulfur yellow 1.0 Succinol BZ 1.0 〃 MZ 1.0 Thickener Required amount Water required (2) Synthetic turf The adhesive composition obtained in (1) was applied to an artificial lawn machine with a polypropylene split yarn as the base cloth and polypropylene as the pile per 1 m 2 Apply 600 g of weight evenly,
It was dried in an oven at 120 ° C. for 20 minutes to prepare artificial grass.
(3) 接着剤組成物の物性の測定 (a) 貯蔵時の粘度安定性 実施例−1と同様に測定した。(3) Measurement of physical properties of adhesive composition (a) Viscosity stability during storage It was measured in the same manner as in Example-1.
(b) マロン式機械的安定性 実施例−1と同様に測定した。(b) Marron Mechanical Stability It was measured in the same manner as in Example-1.
(c) ブリスター特性 (1)で得られた接着剤組成物を基布がポリプロピレンス
プリットヤーン、パイルもポリプロピレンの人工芝生機
裏面に1m2当り見掛重量1000gを均一に塗布し、未
乾燥の人工芝を作成した。(c) The adhesive composition obtained in blister properties (1) was applied uniformly on the back surface of an artificial grass machine with polypropylene split yarn as the base cloth and polypropylene as the pile, and an apparent weight of 1000 g per 1 m 2 was applied to the undried artificial surface. I made grass.
この未乾燥人工芝を温度170℃、熱風速度20m/秒
の乾燥機にて3分間乾燥させ、発生したブリスターを肉
眼にて観察し、下記の級別に判定した。This undried artificial turf was dried for 3 minutes in a dryer at a temperature of 170 ° C. and a hot air speed of 20 m / sec, and the generated blister was observed with the naked eye and judged according to the following grades.
1級:ブリスターの発生が全く認められない。Grade 1: No blister is observed.
8級:ブリスターが全面に多く発生している。 Grade 8: Many blisters occur on the entire surface.
(d) パイル糸の引抜き強度 (2)で得られた人工芝をJISL−1021に準拠し
て、パイル糸の引抜き強度を測定した。(d) Pull-out strength of pile yarn The artificial grass obtained in (2) was measured for pull-out strength of pile yarn according to JIS L-1021.
(e) 耐水強度 (2)で得られた人工芝を60℃の温水に120分間浸漬
した後、ゆるく脱水し、(d)と同様にパイル糸の引抜き
強度を測定した。(e) Water resistance strength The artificial turf obtained in (2) was immersed in warm water at 60 ° C for 120 minutes and then gently dehydrated, and the pull-out strength of the pile yarn was measured as in (d).
(a)〜(e)の結果を表−3に示した。The results of (a) to (e) are shown in Table-3.
ハ.発明の効果 〔本発明の効果〕 本発明にて得られる特定の共重合体ラテックスと、オル
ガノポリシロキサンおよび充填剤とからなるカーペット
バッキング用接着剤組成物は、充分な粘度安定性ならび
に良好な機械的安定性およびブリスター特性を有し、か
つ優れた耐水性ならびに接着強度を兼ね備えている。 C. EFFECTS OF THE INVENTION [Effects of the Invention] An adhesive composition for carpet backing comprising the specific copolymer latex obtained in the present invention, an organopolysiloxane and a filler has sufficient viscosity stability and good mechanical properties. It has excellent stability and blister properties, and also has excellent water resistance and adhesive strength.
Claims (2)
%、エチレン系不飽和カルボン酸0.5〜4.0重量%
およびこれらと共重合可能なモノオレフィン系単量体1
6.0〜64.5重量%を乳化重合し得られた共重合体
の存在下、脂肪族共役ジエン系単量体0〜20重量%お
よびモノオレフィン系単量体80〜100重量%を添加
し重合させた共重合体ラテックス100重量部(固形
分)に対し、オルガノポリシロキサン0.01〜3重量
部および充填剤0〜600重量部を含有することを特徴
とするカーペットバッキング用接着剤組成物。1. Aliphatic conjugated diene monomer 35 to 80% by weight, ethylenically unsaturated carboxylic acid 0.5 to 4.0% by weight
And a mono-olefinic monomer 1 copolymerizable therewith
In the presence of a copolymer obtained by emulsion polymerization of 6.0 to 64.5% by weight, 0 to 20% by weight of an aliphatic conjugated diene monomer and 80 to 100% by weight of a monoolefin monomer are added. Adhesive composition for carpet backing, characterized by containing 0.01 to 3 parts by weight of organopolysiloxane and 0 to 600 parts by weight of filler with respect to 100 parts by weight (solid content) of the polymerized copolymer latex. object.
0〜90重量%である特許請求の範囲第1項記載のカー
ペットバッキング用接着剤組成物。2. The initial monomers to be copolymerized are all 6 monomers.
The carpet backing adhesive composition according to claim 1, which is 0 to 90% by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11264485A JPH0635571B2 (en) | 1985-05-24 | 1985-05-24 | Adhesive composition for car backpacking |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11264485A JPH0635571B2 (en) | 1985-05-24 | 1985-05-24 | Adhesive composition for car backpacking |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61271365A JPS61271365A (en) | 1986-12-01 |
| JPH0635571B2 true JPH0635571B2 (en) | 1994-05-11 |
Family
ID=14591887
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11264485A Expired - Lifetime JPH0635571B2 (en) | 1985-05-24 | 1985-05-24 | Adhesive composition for car backpacking |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0635571B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5323330B2 (en) * | 2006-09-06 | 2013-10-23 | 株式会社イーテック | Composition for artificial turf carpet backing material |
-
1985
- 1985-05-24 JP JP11264485A patent/JPH0635571B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61271365A (en) | 1986-12-01 |
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