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
JP3047153B2 - High strength polyvinyl chloride paste - Google Patents
[go: Go Back, main page]

JP3047153B2 - High strength polyvinyl chloride paste - Google Patents

High strength polyvinyl chloride paste

Info

Publication number
JP3047153B2
JP3047153B2 JP6276713A JP27671394A JP3047153B2 JP 3047153 B2 JP3047153 B2 JP 3047153B2 JP 6276713 A JP6276713 A JP 6276713A JP 27671394 A JP27671394 A JP 27671394A JP 3047153 B2 JP3047153 B2 JP 3047153B2
Authority
JP
Japan
Prior art keywords
parts
weight
polysulfone
pvc
polyvinyl chloride
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP6276713A
Other languages
Japanese (ja)
Other versions
JPH08134304A (en
Inventor
恵美子 藤田
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.)
Yazaki Corp
Original Assignee
Yazaki Corp
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 Yazaki Corp filed Critical Yazaki Corp
Priority to JP6276713A priority Critical patent/JP3047153B2/en
Publication of JPH08134304A publication Critical patent/JPH08134304A/en
Application granted granted Critical
Publication of JP3047153B2 publication Critical patent/JP3047153B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、ポリ塩化ビニル(PV
C)ペーストに関し、詳しくは一般自動車用ドアハーネ
スの結束に使用する加熱により硬化する高強度PVCペ
ーストに関するものである。
BACKGROUND OF THE INVENTION The present invention relates to polyvinyl chloride (PV).
C) More specifically, the present invention relates to a high-strength PVC paste which is hardened by heating and is used for binding door harnesses for general automobiles.

【0002】[0002]

【従来の技術】今までのPVCペーストの主な用途は、
一般自動車ドアハーネスの結束である。PVCペースト
は、PVCに可塑剤と安定剤を加えたものからなり、ワ
イヤーハーネスを数本並べ、PVCペーストを塗布し、
加熱、成形するという結束剤として使用されるが、この
成形品を自動車のドア内やドア付近に固定した時、ドア
の開閉時における激しい衝撃があった場合、それが繰り
返された時にひび割れが生じることがある。
2. Description of the Related Art The main uses of PVC pastes so far are:
It is a unity of general automobile door harness. PVC paste consists of PVC plus plasticizer and stabilizer, several wire harnesses are lined up, PVC paste is applied,
Used as a binder for heating and molding Sometimes.

【0003】[0003]

【発明が解決しようとする課題】本発明は上記問題に鑑
み成されたもので、自動車のドアの繰り返し開閉におけ
るワイヤーハーネスの結束部のひび割れ等を防止可能な
耐衝撃性等に優れた高強度PVCペーストを提供するこ
とを目的とする。
SUMMARY OF THE INVENTION The present invention has been made in view of the above-mentioned problems, and has a high strength excellent in impact resistance and the like which can prevent a crack of a binding portion of a wire harness when a vehicle door is repeatedly opened and closed. It is intended to provide a PVC paste.

【0004】[0004]

【課題を解決するための手段】本発明の目的はポリ塩化
ビニル100重量部、可塑剤200〜300重量部、ポ
リスルホン30〜50重量部および安定剤1〜10重量
部を配合してなる高強度ポリ塩化ビニルペーストにより
達成できる。本発明はPVCペーストにポリスルホンを
特定量配合したことを特徴とし、これにより得られたP
VCペーストは、ワイヤーハーネスの結束剤として硬
化、成形した時、耐衝撃性等に優れた樹脂となることが
わかった。
SUMMARY OF THE INVENTION An object of the present invention is to provide a high strength composition comprising 100 parts by weight of polyvinyl chloride, 200 to 300 parts by weight of a plasticizer, 30 to 50 parts by weight of polysulfone and 1 to 10 parts by weight of a stabilizer. This can be achieved with a polyvinyl chloride paste. The present invention is characterized in that a specific amount of polysulfone is added to a PVC paste, and the P
The VC paste was found to be a resin having excellent impact resistance and the like when cured and molded as a binding agent for a wire harness.

【0005】本発明に使用されるポリスルホンの配合割
合は、PVC100重量部、可塑剤200〜300重量
部、および安定剤1〜10重量部に対し30〜50重量
部、好ましくは、40〜50重量部である。ここで、ポ
リスルホンに割合が30重量部より小さいとポリスルホ
ン無添加品と比べてもあまり樹脂特性が向上せず、50
重量部を越えると引張伸び率(常温24℃)が低下し樹
脂のひび割れが生じ易くなる。
The proportion of the polysulfone used in the present invention is 30 to 50 parts by weight, preferably 40 to 50 parts by weight, per 100 parts by weight of PVC, 200 to 300 parts by weight of a plasticizer and 1 to 10 parts by weight of a stabilizer. Department. Here, if the proportion of the polysulfone is less than 30 parts by weight, the resin properties are not so much improved as compared with the product without the polysulfone, and 50% by weight.
If the amount is more than 10 parts by weight, the tensile elongation (normal temperature: 24 ° C.) is reduced, and the resin is easily cracked.

【0006】本発明に使用されるポリスルホンとして
は、通常、平均重合度(p)が1700〜3700のも
のが挙げられる。本発明の高強度PVCペーストの製造
方法としては、可塑剤中にPVCレジン、ポリスルホン
等の粉体を混ぜあわせる方法が挙げられるが、特に制限
はなく従来公知の製法が適用できる。この混ぜ合わせに
は、先端が羽になっているモーターを使用することが好
ましい。
The polysulfone used in the present invention generally has an average degree of polymerization (p) of 1700 to 3700. Examples of the method for producing the high-strength PVC paste of the present invention include a method in which powders such as PVC resin and polysulfone are mixed into a plasticizer, but there is no particular limitation, and a conventionally known production method can be applied. For this mixing, it is preferable to use a motor whose tip is a wing.

【0007】本発明の高強度PVCペーストに使用され
るPVC、可塑剤、安定剤としては、従来公知のものが
挙げられるが、好ましくは、以下に例示するものが挙げ
られる。PVCとしては、通常、平均重合度p=200
〜1400、特に好ましくは、1100〜1300のも
のが挙げられる。
As the PVC, plasticizer and stabilizer used in the high-strength PVC paste of the present invention, conventionally known ones can be mentioned, and preferably, the followings are exemplified. As PVC, usually, the average degree of polymerization p = 200
To 1400, particularly preferably 1100 to 1300.

【0008】可塑剤としては、ポリエステル系(例え
ば、アジピン酸系ポリエステル〔商品名:PN−350
(旭電化(株)製)、PN−250(旭電化(株)製)
等〕)、エポキシ系(例えば、エポキシ化大豆油、エポ
キシ化アマニ油〔商品名:O−130P(旭電化(株)
製)、O−180A(旭電化(株)製)等〕)等が挙げ
られ、PVC100重量部に対し、200〜300重量
部用いられる。また、該可塑剤はPVC100重量部に
対し特に220〜270重量部を用いると更に効果的で
あり好ましい。
[0008] As the plasticizer, polyester type (for example, adipic acid type polyester [trade name: PN-350]
(Made by Asahi Denka Co., Ltd.), PN-250 (made by Asahi Denka Co., Ltd.)
Etc.)), epoxy type (for example, epoxidized soybean oil, epoxidized linseed oil [trade name: O-130P (Asahi Denka Co., Ltd.)
And O-180A (manufactured by Asahi Denka Co., Ltd.)]), and 200 to 300 parts by weight based on 100 parts by weight of PVC. It is more effective and preferable to use 220 to 270 parts by weight of the plasticizer based on 100 parts by weight of PVC.

【0009】安定剤としては、Ba−Zn系(例えば、
商品名:MARK AP−529(旭電化(株)製)、
MARK AP−536(旭電化(株)製)等〕)、C
a−Zn系(例えば、〔商品名:MARK 593(旭
電化(株)製)、MARKSP−70(旭電化(株)
製)、シナカレッドNLC(品川化工(株)製)
等〕)、Sn系(例えば、ジノルマルオクチル錫メルカ
プト、メチル錫メルカプト〔商品名:MARK 465
(旭電化(株)製)、MARK 1920(旭電化
(株)製)等〕)等が挙げられ、PVC100重量部に
対し、1〜10重量部、好ましくは、3〜7重量部用い
られる。
As a stabilizer, Ba—Zn type (for example,
Product name: MARK AP-529 (manufactured by Asahi Denka Co., Ltd.),
MARK AP-536 (made by Asahi Denka Co., Ltd.)]), C
a-Zn type (for example, [trade name: MARK 593 (manufactured by Asahi Denka Co., Ltd.)), MARKSP-70 (Asahi Denka Co., Ltd.)
Manufactured), Shinaka Red NLC (manufactured by Shinagawa Kako Co., Ltd.)
Etc.)), Sn-based (for example, dinormal octyltin mercapto, methyltin mercapto [trade name: MARK 465]
(Manufactured by Asahi Denka Co., Ltd.), MARK 1920 (manufactured by Asahi Denka Co., Ltd.)], etc., and 1 to 10 parts by weight, preferably 3 to 7 parts by weight, based on 100 parts by weight of PVC.

【0010】本発明の高強度PVCペーストは、必要に
応じて上記成分以外に任意の添加剤(例えば、充填剤
(例えば、炭酸カルシウム等)、難燃剤、(例えば、三
酸化アンチモン等)をPVCに対し、10重量部以下で
使用することができる。
[0010] The high-strength PVC paste of the present invention may contain, if necessary, any additives (for example, filler (for example, calcium carbonate)), a flame retardant (for example, antimony trioxide, etc.) in addition to the above components. To 10 parts by weight or less.

【0011】[0011]

【実施例】以下、本発明の具体的実施例について説明す
るが、本発明はこれに限定されるものではない。尚、
「部」は「重量部」を指す。 実施例1 PVC(p=1300)100部、ポリスルホン(p=
1700)30部、可塑剤(ポリエステル系:PN−3
50)200部、安定剤(Ba−Zn系:MARK A
P−529)5部により均一に混練し、本発明の高強度
PVCペーストを得た。得られたペーストを150℃に
加熱、成形して引張強さ試験(ASTMD638)、引
張伸び率試験(ASTM D638)、衝撃強度試験
(ASTM D256)の規格の試験片を作成し、該規
格に準拠して試験した。その結果を表1に示す。
EXAMPLES The present invention will be described below in detail with reference to Examples, but it should not be construed that the present invention is limited thereto. still,
"Parts" refers to "parts by weight". Example 1 100 parts of PVC (p = 1300), polysulfone (p =
1700) 30 parts, plasticizer (polyester type: PN-3)
50) 200 parts, stabilizer (Ba-Zn system: MARK A)
P-529) 5 parts were uniformly kneaded to obtain a high-strength PVC paste of the present invention. The obtained paste is heated to 150 ° C. and molded to prepare a test piece having a tensile strength test (ASTMD638), a tensile elongation test (ASTM D638), and an impact strength test (ASTM D256). And tested. Table 1 shows the results.

【0012】実施例2 実施例1において、ポリスルホンを40部とした以外は
実施例1と同様に試験片を作成し、同様に試験した。 実施例3 実施例1において、ポリスルホンを50部とした以外は
実施例1と同様に試験片を作成し、同様に試験した。
Example 2 A test piece was prepared and tested in the same manner as in Example 1 except that the polysulfone was changed to 40 parts. Example 3 A test piece was prepared and tested in the same manner as in Example 1 except that the polysulfone was changed to 50 parts.

【0013】比較例1 実施例1において、ポリスルホンを0部とした以外は実
施例1と同様に試験片を作成し、同様に試験した。 比較例2 実施例1において、ポリスルホンを20部とした以外は
実施例1と同様に試験片を作成し、同様に試験した。
Comparative Example 1 A test piece was prepared and tested in the same manner as in Example 1 except that the polysulfone was used in an amount of 0 part. Comparative Example 2 A test piece was prepared and tested in the same manner as in Example 1 except that the polysulfone was changed to 20 parts.

【0014】比較例3 実施例1において、ポリスルホンを60部とした以外は
実施例1と同様に試験片を作成し、同様に試験した。実
施例2〜3、比較例1〜3の結果も表1に示す。尚、
「実」は実施例を、「比」は比較例を示す。
Comparative Example 3 A test piece was prepared and tested in the same manner as in Example 1 except that polysulfone was used in an amount of 60 parts. Table 1 also shows the results of Examples 2-3 and Comparative Examples 1-3. still,
"Actual" indicates an example, and "ratio" indicates a comparative example.

【0015】[0015]

【表1】 [Table 1]

【0016】表1から明らかなように、本発明の高強度
PVCペーストの配合範囲にある実施例1〜3では、ポ
リスルホンを使用しないか過少に用いた比較例1、2に
比べ衝撃強度が改善されたことが分かる。また、比較例
3のように過剰にポリスルホンを使用すると引張り伸び
率が悪化することが分かる。
As is clear from Table 1, the impact strength of Examples 1 to 3 in the compounding range of the high-strength PVC paste of the present invention was improved as compared with Comparative Examples 1 and 2 in which polysulfone was not used or was used in an insufficient amount. You can see that it was done. Further, it can be seen that the tensile elongation deteriorates when polysulfone is used excessively as in Comparative Example 3.

【0017】[0017]

【発明の効果】本発明の高強度PVCペーストは、従来
公知のPVCペーストにポリスルホンを配合するだけと
いう簡明な方法により極めて耐衝撃性の高い樹脂を提供
することができる。特に、自動車ドア部のワイヤーハー
ネスの結束に使用した場合には繰り返し開閉による結束
部のひび割れを効果的に防止することができる。
The high-strength PVC paste of the present invention can provide a resin having extremely high impact resistance by a simple method of simply adding polysulfone to a conventionally known PVC paste. In particular, when used to bind a wire harness in an automobile door, cracks in the binding due to repeated opening and closing can be effectively prevented.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C08L 27/06 C08K 5/10 - 5/12 C08L 81/06 ──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int. Cl. 7 , DB name) C08L 27/06 C08K 5/10-5/12 C08L 81/06

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ポリ塩化ビニル100重量部、可塑剤2
00〜300重量部、ポリスルホン30〜50重量部お
よび安定剤1〜10重量部を配合してなる高強度ポリ塩
化ビニルペースト。
1. 100 parts by weight of polyvinyl chloride, plasticizer 2
A high-strength polyvinyl chloride paste comprising 100 to 300 parts by weight, 30 to 50 parts by weight of polysulfone and 1 to 10 parts by weight of a stabilizer.
JP6276713A 1994-11-10 1994-11-10 High strength polyvinyl chloride paste Expired - Fee Related JP3047153B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6276713A JP3047153B2 (en) 1994-11-10 1994-11-10 High strength polyvinyl chloride paste

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6276713A JP3047153B2 (en) 1994-11-10 1994-11-10 High strength polyvinyl chloride paste

Publications (2)

Publication Number Publication Date
JPH08134304A JPH08134304A (en) 1996-05-28
JP3047153B2 true JP3047153B2 (en) 2000-05-29

Family

ID=17573297

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6276713A Expired - Fee Related JP3047153B2 (en) 1994-11-10 1994-11-10 High strength polyvinyl chloride paste

Country Status (1)

Country Link
JP (1) JP3047153B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111777825A (en) * 2020-05-26 2020-10-16 宜宾天亿新材料科技有限公司 Production method of low-temperature high-toughness high-strength polyvinyl chloride double-wall corrugated pipe

Also Published As

Publication number Publication date
JPH08134304A (en) 1996-05-28

Similar Documents

Publication Publication Date Title
DE3852530T2 (en) Thermoplastic polyester resin composition.
DE69724845T2 (en) Silicone rubber compositions
DE3687844T2 (en) POLYBUTYLENE TEREPHTHALATE COMPOSITION.
TW470770B (en) A flame retardant, halogen-free polymer composition
JP3921448B2 (en) Flame retardant polypropylene resin composition
JP3047153B2 (en) High strength polyvinyl chloride paste
DE69311926T2 (en) Process for producing an electrically conductive organosiloxane composition
DE68925863T2 (en) Flame retardant resin composition based on polyphenylene ether
JPH0645734B2 (en) Fiber-reinforced polypropylene resin composition
DE69701011T2 (en) Thermosetting silicone rubber compound and process for its manufacture
DE68920070T2 (en) Thermoplastic polyester resin composition.
DE69212665T2 (en) Thermoplastic resin compositions
EP0247412B1 (en) Impact-resistant poly(arylene sulphide) compositions
JPH0940829A (en) Flame retardant polyvinyl chloride paste
DE3509568A1 (en) STABILIZED, RED PHOSPHORUS AND THE USE THEREOF FOR FLAME RESISTANT, THERMOPLASTIC POLYAMIDE MOLDS
DE60019382T2 (en) Thermoplastic molding compound
DE69123210T2 (en) Polyester resin mass
JPH08283508A (en) Color masterbatch composition for polyvinyl chloride resin
JP2002212564A (en) Flame retardant, method for producing the same and flame-retardant resin composition containing the flame retardant
DE69123314T2 (en) Polyarylene sulfide resin compositions
EP0128341A2 (en) Stabilised red phosphorus and its use in flame-proof thermoplastic polyamide moulding masses
JP2602722B2 (en) Heat resistant resin composition
JP2988684B2 (en) Thermoplastic polyester resin composition
JP2558540B2 (en) Polypropylene resin composition
JPH10321044A (en) Wire coating material composition

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees