JPH0363536A - Stress sensitive body - Google Patents
Stress sensitive bodyInfo
- Publication number
- JPH0363536A JPH0363536A JP1201062A JP20106289A JPH0363536A JP H0363536 A JPH0363536 A JP H0363536A JP 1201062 A JP1201062 A JP 1201062A JP 20106289 A JP20106289 A JP 20106289A JP H0363536 A JPH0363536 A JP H0363536A
- Authority
- JP
- Japan
- Prior art keywords
- stress
- pas
- present
- biphenylene
- substd
- 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.)
- Pending
Links
- 229920000642 polymer Polymers 0.000 claims abstract description 5
- 229920000412 polyarylene Polymers 0.000 claims abstract description 4
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000000835 fiber Substances 0.000 abstract description 8
- 239000004744 fabric Substances 0.000 abstract description 6
- 239000010408 film Substances 0.000 abstract description 5
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical group C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract description 4
- 238000011161 development Methods 0.000 abstract description 4
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract description 3
- 125000000217 alkyl group Chemical group 0.000 abstract description 2
- -1 biphenylene ether Chemical group 0.000 abstract description 2
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 abstract description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 2
- 230000000007 visual effect Effects 0.000 abstract description 2
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 229910052976 metal sulfide Inorganic materials 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 description 8
- 239000004734 Polyphenylene sulfide Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920000069 polyphenylene sulfide Polymers 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002074 melt spinning Methods 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
Landscapes
- Color Printing (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明はポリアリーレンアルファイド(以下PSと略す
)よりなる新規な応力感知体に関し、特に伸張応力下で
の発色性を有効に利用した応力感知体に関するものであ
る。[Detailed Description of the Invention] <Industrial Application Field> The present invention relates to a novel stress sensing body made of polyarylene alphaide (hereinafter abbreviated as PS), and in particular, the present invention relates to a stress sensing body made of polyarylene alphaide (hereinafter abbreviated as PS). It concerns the sensing body.
〈従来の技術〉
従来、伸張応力を感知又は検出する手段としてはストレ
インゲージと呼ばれる応力を電気信号に変換せしめる方
法が一般的に用いられている。<Prior Art> Conventionally, as a means for sensing or detecting tensile stress, a method called a strain gauge that converts stress into an electrical signal has been generally used.
しかしながらこの方法では応力を感知し計測に用いよう
とする場合には増幅器等を含んだ複雑な電気回路など高
価な設備を必要としていたためその用途が限定される等
の欠点があった。However, this method has disadvantages such as limited use because it requires expensive equipment such as complicated electric circuits including amplifiers and the like in order to sense stress and use it for measurement.
〈発明が解決しようとする課題〉
本発明は伸張応力を感知するためにストレインゲージの
如き複雑で高価な電気回路の必要性を解消し人間が目視
により応力を判定できるような応力感知体を提供せんと
するものである。<Problems to be Solved by the Invention> The present invention eliminates the need for a complicated and expensive electric circuit such as a strain gauge to sense tensile stress, and provides a stress sensing body that allows humans to visually determine stress. This is what I am trying to do.
く課題を解決するための手段〉
本発明者らはPASからなる繊維、布帛又はフィルムが
伸張応力下で特定の波長の発色が起こることを見出し本
発明に到達した。Means for Solving the Problems The present inventors have arrived at the present invention by discovering that fibers, fabrics, or films made of PAS develop color at a specific wavelength under tensile stress.
即ち、本発明はPAS重合体からなる応力感知体であっ
て伸張応力下で特定の波長の光の反射強度が変化する応
力感知体である。PASの形態としては繊維、布帛又は
フィルム等があげられる。That is, the present invention is a stress sensing body made of a PAS polymer, which changes the reflection intensity of light of a specific wavelength under tensile stress. Examples of the form of PAS include fibers, fabrics, and films.
本発明においてPASとは隣接する環原子間に不飽和基
を有する多ハロ置換の環状化合物とアルカリ金属サルフ
ァイドとを有機極性溶媒中で反応せしめることによって
得られる一R−8−基(ただしR:フェニレン、ビフェ
ニレン、ナフタレン、ビフェニレンエーテルまたはそれ
らの炭素数1〜6の低級アルキル置換誘導体である)を
繰返し単位として有する重合体であり、代表的にはたと
えば米国特許第3354129号明細書に詳しく述べら
れているものが使用できるがPASの絶唱に含められる
ものは全て本発明の対象に含められる。なお本発明にお
いてはRがフェニレン基であるポリフェニレンサルファ
イド(以下PPSという)が特に好ましい。In the present invention, PAS refers to a monoR-8- group (wherein R: It is a polymer having as a repeating unit phenylene, biphenylene, naphthalene, biphenylene ether or a lower alkyl substituted derivative thereof having 1 to 6 carbon atoms, and is typically described in detail in US Pat. No. 3,354,129. However, anything that can be included in PAS's Zessho is included in the scope of the present invention. In the present invention, polyphenylene sulfide (hereinafter referred to as PPS) in which R is a phenylene group is particularly preferred.
PASが伸張応力下で特定波長の発色を呈する原因に関
しては鋭意検討中であるが明確な結論は得られてない。The cause of PAS exhibiting coloration at a specific wavelength under tensile stress is currently under active investigation, but no clear conclusion has been reached.
しかしながら特定波長の光の反射強度が変化することは
後述する方法で確認され又人間の目視により容易に判定
可能である。However, the fact that the reflected intensity of light of a specific wavelength changes can be confirmed by the method described later, and can be easily determined by human visual observation.
伸張応力の変化に伴う発色性は繊維、布帛、フィルム等
の形態で発現しやすく、感知体としての用途もひも、ベ
ルト、テープ類等多岐に渡って展開が可能である。Coloring properties associated with changes in elongation stress are easily expressed in the form of fibers, fabrics, films, etc., and can be used in a wide variety of applications such as strings, belts, and tapes.
PASの伸張応力下での発色は青緑色に近いものであり
、物理的に検出するには分光光度計での630mμの反
射率を中心に低下が認められ肉眼でも容易に判る。The color development of PAS under tensile stress is close to blue-green, and in terms of physical detection, a decrease in the reflectance of 630 mμ with a spectrophotometer is observed, which is easily seen with the naked eye.
次に本発明のPASよりなる応力感知体の製造方法につ
いて述べてる。本方法によれば前記した応力感知体が得
られるが、その製造方法は下記の内容に限定されるもの
ではない。Next, a method for manufacturing a stress sensor made of PAS of the present invention will be described. According to this method, the stress sensing body described above can be obtained, but the manufacturing method thereof is not limited to the following content.
極限粘度0.20以上のPASポリマーを290〜31
0°Cに溶融した後紡糸し、冷却して未延伸糸を得る。PAS polymer with an intrinsic viscosity of 0.20 or more from 290 to 31
After melting at 0°C, it is spun and cooled to obtain an undrawn yarn.
得られた未延伸糸を紡糸に連続して、あるいは−旦巻き
取った後延伸する。このしこの際、延伸第10−ラーを
PASのガラス転移点上℃に加熱しておき、第20−ラ
ーで2〜4倍に延伸して引取り、つづいて第20−ラー
と第30−ラーとの間で1〜10%弛緩させつつ150
〜200℃に熱したプレートに接触させて熱処理してP
AS延伸糸を得る。The obtained undrawn yarn is drawn either continuously after spinning or after being wound up once. At this time, the 10th drawing roller is heated to a temperature above the glass transition point of PAS, and the 20th drawing roller is stretched 2 to 4 times and taken off, followed by the 20th drawing and 30th drawing. 150 while relaxing 1-10% between the
Heat-treated by contacting with a plate heated to ~200℃
Obtain AS drawn yarn.
又溶融紡糸に先だっであるいは本発明の応力感知体製造
工程中に必要に応じ光安定剤、酸化防止剤、帯電防止剤
、染色性向上剤或は接着性向上剤等を配合することがで
き、配合の如何によって本発明の特性に重大な影響を与
えるもの以外は、全て利用できる。In addition, a light stabilizer, an antioxidant, an antistatic agent, a dyeability improver, an adhesion improver, etc. may be added as necessary prior to melt spinning or during the process of manufacturing the stress sensor of the present invention. All of them can be used, except those that have a significant effect on the characteristics of the present invention depending on their formulation.
こうして得たPAS繊維はそのままで応力感知体として
使用することができる。又、合糸、撚糸により糸状とし
たり、又、織編物に加工して使用することも可能である
。さらに公知の方法を用いて短繊維不織布又は長繊維不
織布(いわゆるスパンボンド)としたり、フィルム状に
成型することによって得られるものもすべて応力感知体
として使用可能である。The PAS fiber thus obtained can be used as it is as a stress sensor. It is also possible to use it by making it into a filament by doubling or twisting it, or by processing it into a woven or knitted fabric. Further, any material obtained by forming short fiber nonwoven fabric or long fiber nonwoven fabric (so-called spunbond) using a known method, or by molding it into a film can also be used as a stress sensor.
次に本発明に係る各数値の測定方法あるいは評価方法に
ついて述べる。Next, a method for measuring or evaluating each numerical value according to the present invention will be described.
(極限粘度)
1−クロロナフタレンにPAII度が0.5〜1 g/
d fになるように溶解してサンプル溶液を調整し、2
0′Cの温度での氷落下秒数6〜7秒のオスワルド粘度
計を用いて溶液粘度を測定する。(Intrinsic viscosity) PAII degree of 1-chloronaphthalene is 0.5 to 1 g/
Adjust the sample solution by dissolving it so that d f, 2
The solution viscosity is measured using an Oswald viscometer with an ice fall time of 6-7 seconds at a temperature of 0'C.
測定に際し同一の粘度計を用い0.5g/cl及びIg
/dfの溶液20m1の落下時間より極限粘度を求める
。(分光反射率)
自記分光光度計(日立 EPR−2形)を用いて可視域
400〜760mμにおける標準サンプルに対する試料
の反射率を測定する。0.5g/cl and Ig using the same viscometer for measurement
The intrinsic viscosity is determined from the falling time of 20 ml of solution of /df. (Spectral Reflectance) The reflectance of the sample with respect to the standard sample in the visible range of 400 to 760 mμ is measured using a self-recording spectrophotometer (Hitachi EPR-2 type).
以上述べてきたようにPASを繊維、布帛、又はフィル
ムに加工した後、伸張応力下で可視域の発色を利用する
ことにより容易に応力を検出できる感知体を提供するこ
とができる。As described above, after processing PAS into fibers, fabrics, or films, it is possible to provide a sensor that can easily detect stress by utilizing color development in the visible range under tensile stress.
〈実施例〉
実施例1
極限粘度0.22のPPSチップを原料とし孔径0.3
3m諺、孔数24の紡糸口金より300℃で溶融紡糸後
巻取り、引続いて95℃に保たれたル10−ラーと常温
の第20−ラーとで2.8倍に延伸し、さらに第30−
ラーとの間に設けた200℃のホットプレートを用いて
5%の弛緩熱処理を施して70デニール×24フイラメ
ントの延伸フィラメントを得た。得られた延伸フィラメ
ント糸を各種の応力下で伸張した時の分光反射率を第1
図に示す。また630mμの反射率と応力との関係を第
2図に示す。<Example> Example 1 A PPS chip with an intrinsic viscosity of 0.22 is used as a raw material, and a pore diameter of 0.3
After melt spinning at 300°C from a spinneret with 24 holes, it was wound up, and then stretched to 2.8 times with a 10-layer kept at 95°C and a 20th-layer at room temperature. 30th-
A 5% relaxation heat treatment was performed using a 200° C. hot plate provided between the roller and the roller to obtain a drawn filament of 70 denier×24 filaments. The spectral reflectance when the obtained drawn filament yarn was stretched under various stresses was calculated as
As shown in the figure. Furthermore, the relationship between the reflectance at 630 mμ and the stress is shown in FIG.
第1図および第2図から明らかなように、本発明の応力
感知体は伸張時に特定の波長の反射率が低下するため、
肉眼で感知体の応力状態を知ることができる。As is clear from FIGS. 1 and 2, when the stress sensing body of the present invention is stretched, the reflectance of a specific wavelength decreases.
The stress state of the sensor can be seen with the naked eye.
〈発明の効果〉
本発明によればPASという軽量かつ安価な有機素材を
用いることにより容易に伸張応力に対して発色が認めら
れ応力感知体として有効な手段となり得るものである。<Effects of the Invention> According to the present invention, by using a lightweight and inexpensive organic material called PAS, color development is easily observed in response to stretching stress, and it can be an effective means as a stress sensor.
第1図は各種(40kg/ d、 50 kg/ w
J)の応力下におけるフィラメント糸の波長と分光反射
率の関係を示す。
第2図はフィラメント糸の応力と630mμの反射率と
の関係を示す。Figure 1 shows various types (40 kg/d, 50 kg/w
The relationship between the wavelength and spectral reflectance of the filament yarn under the stress of J) is shown. FIG. 2 shows the relationship between the stress of the filament yarn and the reflectance at 630 mμ.
Claims (1)
。Stress sensing body made of polyarylene sulfide polymer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1201062A JPH0363536A (en) | 1989-08-01 | 1989-08-01 | Stress sensitive body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1201062A JPH0363536A (en) | 1989-08-01 | 1989-08-01 | Stress sensitive body |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0363536A true JPH0363536A (en) | 1991-03-19 |
Family
ID=16434751
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1201062A Pending JPH0363536A (en) | 1989-08-01 | 1989-08-01 | Stress sensitive body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0363536A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001106984A (en) * | 1999-10-01 | 2001-04-17 | Nitto Denko Corp | Adhesive film or sheet for detection of local displacement |
JP2017024376A (en) * | 2015-07-28 | 2017-02-02 | 大日本印刷株式会社 | Laminate |
-
1989
- 1989-08-01 JP JP1201062A patent/JPH0363536A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001106984A (en) * | 1999-10-01 | 2001-04-17 | Nitto Denko Corp | Adhesive film or sheet for detection of local displacement |
JP2017024376A (en) * | 2015-07-28 | 2017-02-02 | 大日本印刷株式会社 | Laminate |
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