Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPH0240259B2 - DODENSEIKAAPETSUTOYORAUCHISOSEIBUTSU - Google Patents
[go: Go Back, main page]

JPH0240259B2 - DODENSEIKAAPETSUTOYORAUCHISOSEIBUTSU - Google Patents

DODENSEIKAAPETSUTOYORAUCHISOSEIBUTSU

Info

Publication number
JPH0240259B2
JPH0240259B2 JP16450985A JP16450985A JPH0240259B2 JP H0240259 B2 JPH0240259 B2 JP H0240259B2 JP 16450985 A JP16450985 A JP 16450985A JP 16450985 A JP16450985 A JP 16450985A JP H0240259 B2 JPH0240259 B2 JP H0240259B2
Authority
JP
Japan
Prior art keywords
pvc
parts
composition
weight
paste
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
Application number
JP16450985A
Other languages
Japanese (ja)
Other versions
JPS6225146A (en
Inventor
Toshikazu Takigawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Suminoe Co Ltd
Original Assignee
Suminoe Textile Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Suminoe Textile Co Ltd filed Critical Suminoe Textile Co Ltd
Priority to JP16450985A priority Critical patent/JPH0240259B2/en
Publication of JPS6225146A publication Critical patent/JPS6225146A/en
Publication of JPH0240259B2 publication Critical patent/JPH0240259B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は、導電性カーペツトに用いる裏打ち組
成物に関するものである。 (従来の技術) 導電性カーペツト用としてペースト法で製造さ
れるPVC樹脂にカーボンブラツク粒子を配合し、
導電性を付与する試みは広く行われているが、所
望の体積固有抵抗値あるいは、表面抵抗値を得る
ためには、多量のカーボンブラツクを配合する必
要があるが、吸油量が大きく、中でも特に、吸油
量の大きいketjen blackなどを使用することが多
い。 (発明が解決しようとする問題点) このような場合、カーボンブラツク粒子により
PVC組成物ペースト中の可塑剤が吸収され、当
該ペーストの粘度が非常に高くなり、カーペツト
にコーテイングする際に、ペーストがかすれたり
気泡を巻きこんだりして加工が極めて困難であつ
た。 本発明は、上記の問題に対しコーテイングが充
分に可能な粘度で、かつ帯電防止には充分な電気
特性を持つPVC樹脂組成物を提供するものであ
る。 (問題点を解決するための手段) 本発明は、ペースト用塩化ビニル樹脂(PVC)
あるいは酢酸ビニル−塩化ビニル共重合樹脂
(PVAc−PVC)100重量部、アルキル鎖の炭素数
が7〜10であるフタル酸ジアルキル可塑剤40〜80
重量部からなる組成物()と 含窒素非イオン系界面活性剤あるいは3級又は
4級アンモニウム塩を主成分としたカチオン系界
面活性剤1〜10wt%とカーボンブラツク1〜
10wt%を含有し、アルキル鎖の炭素数が7〜10
であるフタル酸ジアルキル可塑剤を分散媒とした
トナー30〜60重量部からなる組成物()とを混
合したPVC組成物であつて、その粘度がBM型粘
度計(#4ローター6r.p.m)での値が20℃で
25000c.p.以下で、かつそのペーストを加熱する
ことによりゲル化、溶融させた後の当該樹脂の体
積固有抵抗値および表面抵抗の値がそれぞれ104
〜106Ω−cm,105〜107Ωであることを特徴とする
導電性カーペツト用裏打ち組成物である。 PVCあるいはPVAc−PVCについては、例え
ば、平均重合度()=1500の樹脂70重量部、
()=1000の増量用PVCレジン30重量部、2−
エチルヘキシルフタレート(DOP)92重量部、
カーボンブラツク4.5重量部、その他の助剤5.5重
量部の配合で引張強度が57.1Kg/cm2が得られる。
(シート厚 約1.5mmオーブン中で195℃×4分で
ゲル化、溶融、試験法JISK−6300。) 可塑剤はペースト加工ではブリード性あるいは
コストの点からフタル酸系の可塑剤が広く使用さ
れている。アルキル鎖が短いフタル酸ジアルキル
可塑剤は、組成物ペーストの貯蔵安定性が悪く、
また揮発原料が大きい。またアルキル鎖が余り長
くなるとPVC樹脂との相容性が悪くなり、ゲル
化速度も遅れるので多量のカーボンブラツクが入
りにくい。従つて、一般のPVC組成物に比べ、
可塑剤の使用量が多くなるカーボンブラツク混入
配合では使用しにくい。 これらの問題のため、フタル酸ジアルキル鎖の
炭素数が7〜10が望ましい。 可塑剤の配合量は、コーテイング加工に適する
BM型粘度計(#4,6r.p.m)=25000cp/20℃以
下を保つには、トナー中の可塑剤も加えて好まし
くは90〜105重量部配合する。またコストダウン
のために粘度、および電気的物性に影響のない範
囲で無機フイーラーを配合しても良く、また、熱
安定剤としてCa系を1〜2重量部、吸湿剤など
も必要に応じて加え組成物()とする。 トナーは、高導電性カーボンブラツク例えば
Ketjen blackを1〜10wt%、含窒素非イオン系
界面活性剤あるいは、3級又は4級アンモニウム
塩を主成分としたカチオン系界面活性剤1〜
10wt%を含有し、アルキル鎖の炭素数が7〜10
であるフタル酸ジアルキル可塑剤分散体をロール
ミル等でカーボンブラツク粒子の二次凝集を解
き、分散剤の吸着膜をカーボンブラツク粒子表面
に形成せしめ組成物()とし、安定で流動性の
良好なものとし、()と()を混合する。こ
のトナーの流動性を良くし粘度を下げることは、
PVCペースト組成物の粘度を下げることにもな
り重要である。 この目的のためには、分散剤の選定が重要であ
りKetjen black粒子表面への吸着の点では、窒
素原子を含む非イオン系界面活性剤又は3級ある
いは4級アンモニウム塩系のカチオン系界面活性
剤が粒子表面への吸着が大きいため、安定な吸着
膜が形成され流動性のよいトナーが得られた。 上記のごとく、トナー以外のPVCペースト組
成物()は予めミキサーでブレンドし、そのも
のに組成物()を所定量加え低速撹拌で均一に
混合させるか、あるいは予めミキサーでブレンド
された組成物()と組成物()をラインミキ
サーによりブレンドする。 (実施例) 以下、本発明の実施例と比較例の配合組成とそ
の粘度および電気特性を示す。
INDUSTRIAL APPLICATION FIELD OF THE INVENTION The present invention relates to backing compositions for use in conductive carpets. (Prior technology) Carbon black particles are blended into PVC resin manufactured by a paste method for use in conductive carpets.
Attempts to impart electrical conductivity have been widely made, but in order to obtain the desired volume resistivity or surface resistance, it is necessary to incorporate a large amount of carbon black, but carbon black has a large oil absorption capacity, and in particular , ketjen black, which has a high oil absorption capacity, is often used. (Problem to be solved by the invention) In such a case, carbon black particles
The plasticizer in the PVC composition paste was absorbed, and the viscosity of the paste became very high. When coating a carpet, the paste became blurred and air bubbles were involved, making it extremely difficult to process. The present invention solves the above problems by providing a PVC resin composition that has a viscosity sufficient for coating and has sufficient electrical properties to prevent static electricity. (Means for solving the problems) The present invention uses vinyl chloride resin (PVC) for paste.
Or 100 parts by weight of vinyl acetate-vinyl chloride copolymer resin (PVAc-PVC), 40-80 parts of dialkyl phthalate plasticizer whose alkyl chain has 7 to 10 carbon atoms.
1 to 10 wt % of a cationic surfactant containing a nitrogen-containing nonionic surfactant or a tertiary or quaternary ammonium salt as a main component, and 1 to 10 wt % of carbon black.
Contains 10wt%, and the number of carbon atoms in the alkyl chain is 7 to 10.
A PVC composition mixed with a composition () consisting of 30 to 60 parts by weight of toner using a dialkyl phthalate plasticizer as a dispersion medium, the viscosity of which is determined by a BM type viscometer (#4 rotor 6 rpm). The value at 20℃
25000c.p. or less, and the volume resistivity and surface resistance of the resin after gelling and melting by heating the paste are 10 4
10 6 Ω-cm and 10 5 to 10 7 Ω. For PVC or PVAc-PVC, for example, 70 parts by weight of resin with average degree of polymerization () = 1500,
() = 30 parts by weight of PVC resin for bulking of 1000, 2-
92 parts by weight of ethylhexyl phthalate (DOP),
A tensile strength of 57.1 Kg/cm 2 can be obtained by blending 4.5 parts by weight of carbon black and 5.5 parts by weight of other auxiliaries.
(Sheet thickness: Approximately 1.5 mm. Gelification and melting in an oven at 195℃ for 4 minutes, test method JISK-6300.) Phthalate-based plasticizers are widely used in paste processing due to bleedability and cost considerations. ing. Dialkyl phthalate plasticizers with short alkyl chains have poor storage stability of composition pastes;
Also, volatile raw materials are large. Furthermore, if the alkyl chain is too long, the compatibility with the PVC resin will be poor and the gelation rate will be delayed, making it difficult to incorporate a large amount of carbon black. Therefore, compared to general PVC compositions,
It is difficult to use in formulations containing carbon black, which requires a large amount of plasticizer. Because of these problems, it is desirable that the dialkyl phthalate chain has 7 to 10 carbon atoms. The amount of plasticizer blended is suitable for coating processing.
In order to maintain the BM type viscometer (#4, 6 r.pm) = 25000 cp/20°C or less, a plasticizer in the toner is also added, preferably in an amount of 90 to 105 parts by weight. In order to reduce costs, an inorganic filler may be added within a range that does not affect the viscosity and electrical properties. Also, 1 to 2 parts by weight of Ca-based heat stabilizer and a moisture absorbent may be added as necessary. Add composition (). The toner is made of highly conductive carbon black, e.g.
1 to 10 wt% of Ketjen black, a nitrogen-containing nonionic surfactant, or a cationic surfactant containing tertiary or quaternary ammonium salt as the main component.
Contains 10wt%, and the number of carbon atoms in the alkyl chain is 7 to 10.
A dispersion of a dialkyl phthalate plasticizer is deagglomerated from the carbon black particles using a roll mill, etc., and an adsorption film of the dispersant is formed on the surface of the carbon black particles to form a composition (), which is stable and has good fluidity. and mix () and (). To improve the fluidity and lower the viscosity of this toner,
This is also important because it reduces the viscosity of the PVC paste composition. For this purpose, the selection of a dispersant is important.In terms of adsorption to the Ketjen black particle surface, nonionic surfactants containing nitrogen atoms or cationic surfactants such as tertiary or quaternary ammonium salts are recommended. Since the agent was highly adsorbed on the particle surface, a stable adsorption film was formed and a toner with good fluidity was obtained. As mentioned above, the PVC paste composition () other than toner can be blended in advance with a mixer, and a predetermined amount of the composition () can be added thereto and mixed uniformly with low-speed stirring, or the composition () can be blended in advance with a mixer. and composition () are blended using a line mixer. (Example) The compositions, viscosity, and electrical properties of Examples and Comparative Examples of the present invention are shown below.

【表】【table】

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】 1 ペースト用塩化ビニル樹脂(PVC)あるい
は酢酸ビニルー塩化ビニル共重合樹脂(PVAc−
PVC)100重量部、アルキル鎖の炭素数が7〜10
であるフタル酸ジアルキル可塑剤40〜80重量部か
らなる組成物()と 含窒素非イオン系界面活性剤あるいは3級又は
4級アンモニウム塩を主成分としたカチオン系界
面活性剤1〜10wt%とカーボンブラツク1〜
10wt%を含有しアルキル鎖の炭素数が7〜10で
あるフタル酸ジアルキル可塑剤を分散媒としたト
ナー30〜60重量部からなる組成物()とを混合
したPVC組成物であつて、その粘度がBM型粘度
計(#4 ローター6r.p.m)での値が20℃で
25000c.p.以下でかつ、そのペーストを加熱する
ことによりゲル化、溶融させた後の当該樹脂の体
積固有抵抗値および表面抵抗値がそれぞれ104
106Ω−cm,105〜107Ωであることを特徴とする導
電性カーペツト用裏打ち組成物。
[Claims] 1. Vinyl chloride resin (PVC) for paste or vinyl acetate-vinyl chloride copolymer resin (PVAc-
PVC) 100 parts by weight, the number of carbon atoms in the alkyl chain is 7 to 10
A composition () consisting of 40 to 80 parts by weight of a dialkyl phthalate plasticizer, and 1 to 10 wt% of a cationic surfactant containing a nitrogen-containing nonionic surfactant or a tertiary or quaternary ammonium salt as a main component. Carbon black 1~
A PVC composition mixed with a composition () consisting of 30 to 60 parts by weight of a toner in which a dispersion medium is a dialkyl phthalate plasticizer containing 10 wt% and having an alkyl chain of 7 to 10 carbon atoms, The viscosity is measured at 20℃ using a BM type viscometer (#4 rotor 6r.pm).
25000 c.p. or less, and the volume resistivity and surface resistance of the resin after gelling and melting by heating the paste are 10 4 to 10, respectively.
10 6 Ω-cm, 10 5 to 10 7 Ω.
JP16450985A 1985-07-24 1985-07-24 DODENSEIKAAPETSUTOYORAUCHISOSEIBUTSU Expired - Lifetime JPH0240259B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16450985A JPH0240259B2 (en) 1985-07-24 1985-07-24 DODENSEIKAAPETSUTOYORAUCHISOSEIBUTSU

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16450985A JPH0240259B2 (en) 1985-07-24 1985-07-24 DODENSEIKAAPETSUTOYORAUCHISOSEIBUTSU

Publications (2)

Publication Number Publication Date
JPS6225146A JPS6225146A (en) 1987-02-03
JPH0240259B2 true JPH0240259B2 (en) 1990-09-11

Family

ID=15794510

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16450985A Expired - Lifetime JPH0240259B2 (en) 1985-07-24 1985-07-24 DODENSEIKAAPETSUTOYORAUCHISOSEIBUTSU

Country Status (1)

Country Link
JP (1) JPH0240259B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07870B2 (en) * 1988-11-14 1995-01-11 株式会社クラレ Suede-like seat
JP2657681B2 (en) * 1988-12-08 1997-09-24 三菱バーリントン 株式会社 Backing composition for conductive carpet
JP2537742B2 (en) * 1992-12-14 1996-09-25 株式会社関西テック Oil water separator

Also Published As

Publication number Publication date
JPS6225146A (en) 1987-02-03

Similar Documents

Publication Publication Date Title
ES2913713T3 (en) Powder formulation of water soluble polymers having improved dispersion properties
JPS58132058A (en) Method for preparing conductive coating composition
JPH0240259B2 (en) DODENSEIKAAPETSUTOYORAUCHISOSEIBUTSU
CN110305424B (en) A kind of antistatic home decoration board and preparation method thereof
US3483156A (en) Method of preparing tape joint cement
CN113861594A (en) Flame-retardant high-temperature-resistant PVC (polyvinyl chloride) film for graphene electrothermal film and preparation method thereof
CN108530809A (en) Preparation method of CPVC modified blend material
JP2657681B2 (en) Backing composition for conductive carpet
JPH0136854B2 (en)
CN110483915B (en) 105 ℃ semiconductive PVC material for automobile coaxial cable and preparation method thereof
CN101855275A (en) Acrylic plastisol viscosity reducers
JP3408853B2 (en) Aqueous emulsion paint
JPH06128492A (en) Vibration-damping material composition
JP2024142174A (en) Composition for vinyl chloride resin film and vinyl chloride resin film
JPH0611830B2 (en) Organosol composition and method for producing the same
JPH10176087A (en) Plastisol composition
JPH02151646A (en) Plastisol composition
JPS63182362A (en) conductive paste sol
JPH07278391A (en) Antistatic vinylic polymer composition containing chlorine and molding
JPH062419A (en) Floor material
CN121554935A (en) Environment-friendly antistatic agent for TPEE material and preparation method thereof
CN119931167A (en) Composite plasticizer and method for preparing polyvinyl chloride plastisol for inhibiting plasticizer migration in polyvinyl chloride paste resin products
JPS62291362A (en) Conductive floor
JP2710109B2 (en) Plasticizer with improved antistatic properties
JPS62223253A (en) Polyvinyl chloride resin composition for pasting