JPS6130710B2 - - Google Patents
Info
- Publication number
- JPS6130710B2 JPS6130710B2 JP7649779A JP7649779A JPS6130710B2 JP S6130710 B2 JPS6130710 B2 JP S6130710B2 JP 7649779 A JP7649779 A JP 7649779A JP 7649779 A JP7649779 A JP 7649779A JP S6130710 B2 JPS6130710 B2 JP S6130710B2
- Authority
- JP
- Japan
- Prior art keywords
- amount
- insulator
- conductivity
- wetting
- contaminants
- 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
- 239000012212 insulator Substances 0.000 claims description 25
- 239000000356 contaminant Substances 0.000 claims description 18
- 238000009736 wetting Methods 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 12
- 238000005259 measurement Methods 0.000 claims description 11
- 238000011109 contamination Methods 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 238000010586 diagram Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Testing Relating To Insulation (AREA)
- Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
Description
【発明の詳細な説明】
本発明は湿潤式碍子汚損測定における適正湿潤
量制御方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for controlling an appropriate amount of moisture in wet-type insulator stain measurement.
送電線路等に使用される碍子が海塩等によつて
自然汚損され閃絡する事故は広範囲にわたるた
め、その防止対策は電力供給上重要なものとなつ
ている。その防止対策を行なう上で碍子の汚損量
あるいは汚損状態を把握することは重要なことで
ある。しかし実使用碍子の汚損量を直接測定する
ことは困難であるので、実使用碍子と同一条件下
に自然暴露されたパイロツト碍子の汚損量を知
り、実使用碍子の汚損量を推定する方法が一般的
である。 BACKGROUND ART Accidents in which insulators used in power transmission lines, etc. are naturally contaminated by sea salt and the like and cause flashing are widespread, and preventive measures have become important in the power supply. In order to take preventive measures, it is important to understand the amount or state of contamination of the insulator. However, it is difficult to directly measure the amount of contamination on actually used insulators, so a common method is to estimate the amount of contamination on a pilot insulator that has been exposed to nature under the same conditions as the actually used insulator. It is true.
パイロツト碍子に付着した汚損物を測定する方
法としては従来より、筆等により汚損物を碍子下
面から洗い流しその汚損物の量を測定する方法や
碍子に汚損物を付着させたまま人工湿潤しその導
電度が汚損量により相違することを利用して汚損
物を測定する方法などがあつた。後者の方法は、
パイロツト碍子の汚損物を洗い流さず付着させた
まま測定するため、汚損度の経時的変化を測定で
き、汚損管理上有利であり、また自動測定及び遠
隔測定ができるという利点がある。 Conventional methods for measuring contaminants attached to pilot insulators include washing the contaminants from the underside of the insulator with a brush or measuring the amount of contaminants, or artificially moistening the insulator with contaminants still attached to the insulator and measuring its conductivity. There are methods to measure soiling by taking advantage of the fact that the degree of soiling differs depending on the amount of soiling. The latter method is
Since the measurement is performed while the soiled matter remains on the pilot insulator without being washed away, it is possible to measure changes in the degree of fouling over time, which is advantageous in terms of pollution control, and also has the advantage of being able to perform automatic measurement and remote measurement.
この湿潤法による汚損測定では、パイロツト碍
子下面に水蒸気、スプレーあるいは噴霧等の方法
で水分を与え、汚損物を湿潤して碍子下面に設け
た電極間の導電度を測定することにより汚損量を
検知するものであるが、その浸潤度が低いと汚損
物が溶解しないので導電度が測定できないし、高
過ぎると碍子下面から水滴が滴下し、汚損物が水
滴と共に落下して正確な測定ができなくなるので
湿潤度は適正なものとしなければならない。従
来、どの程度の湿潤度にするかは測定者の勘に頼
つたり、また付着させる水分の総量を一定にする
などの方法が採られていたものであるが、温度、
湿度や汚損度の相違により適正湿潤度が変わるの
で正確な適正湿潤量にすることが困難であつた。 In stain measurement using this wet method, moisture is applied to the underside of the pilot insulator using methods such as steam, spray, or mist, and the amount of contamination is detected by moistening the soiled material and measuring the conductivity between electrodes provided on the underside of the insulator. However, if the degree of infiltration is low, the conductivity cannot be measured because the contaminants will not dissolve, and if it is too high, water droplets will drip from the bottom of the insulator, and the contaminants will fall with the water droplets, making accurate measurements impossible. Therefore, the moisture level must be appropriate. In the past, methods such as relying on the intuition of the measurer to determine the degree of humidity or keeping the total amount of moisture deposited constant were used;
Since the appropriate humidity level changes depending on the humidity and degree of contamination, it has been difficult to obtain an accurate moisture level.
本発明は、このような従来の問題を解消し、湿
潤量を最適に制御することのできる方法を提供す
ることを目的とするものである。 It is an object of the present invention to provide a method that can solve these conventional problems and optimally control the amount of wetting.
以下本発明を説明すれば、電解質ならびに導電
性の汚損物を水分により湿潤させる場合に、湿潤
が進めば一般にその導電度は大きくなる傾向にあ
る。第1図はその関係を図示したものである。さ
らに湿潤が進むと導電度はほぼ一定の値をとり、
この値と付着汚損物の量とは比例関係にある。こ
の関係により付着汚損物の量を測定しようとする
のが測定原理である。しかしながらこの導電度が
ほぼ一定の値となる前の状態すなわち湿潤量が小
の場合は測定値のバラツキとなり好ましくなく、
又さらに湿潤度を増すと過湿潤となり汚損物の滴
下となる。すなわち導電度がほぼ一定となる湿潤
量から滴下を生じない程度までの適度の湿潤量に
より湿潤させ、測定する事が望ましい。第2図は
付着水分量(蒸気による湿潤の場合は蒸気量)と
導電度との関係である。1は碍子面がある程度湿
潤している場合、2は乾燥している場合である。
この様に適性湿潤になるには湿潤開始前の碍子面
の湿潤状態等によりまちまちでたとえば2の場合
にあわせて付着水分量を供給すると1の場合は過
湿潤による汚損物の滴下の恐れがあり、1の場合
にあわせると2の場合は湿潤量の不足となり測定
値として採用できず諸条件に応じて適性湿潤する
事は非常に困難である。ところがここで付着水分
量に対する導電度の変化をみると、その変化は適
性湿潤に近づくにつれて小さくなり、これは湿潤
開始前の碍子の湿潤状態にかかわらず同傾向であ
る。本発明はこれを利用し湿潤量を制御しようと
するものである。すなわち汚損物の湿潤進行状態
の導電度の変化量又は変化率を検出し、その変化
がある値以下になつたら適正湿潤になつたと判断
し、湿潤量を制御しようとするものである。第2
図における1′,2′はそれぞれ1,2の場合の変
化率の変化を示すものである。この原理である
為、測定前の碍子の湿潤状態、汚損量の大小、そ
の他の影響を受けず汚損量に応じた適切な湿潤と
なる様に制御が可能となる。 To explain the present invention below, when an electrolyte and conductive contaminants are moistened with water, the conductivity generally tends to increase as the wetting progresses. FIG. 1 illustrates this relationship. As wetting further progresses, the conductivity takes on a nearly constant value,
There is a proportional relationship between this value and the amount of adhered contaminants. The principle of measurement is to measure the amount of attached contaminants based on this relationship. However, in a state before this conductivity reaches a nearly constant value, that is, when the amount of wetness is small, the measured values will vary, which is undesirable.
Furthermore, if the degree of humidity is further increased, it becomes over-humidified, resulting in dripping of contaminants. That is, it is desirable to wet the conductivity with an appropriate amount ranging from a wet amount that makes the conductivity substantially constant to a degree that does not cause dripping, and then perform the measurement. FIG. 2 shows the relationship between the amount of adhered moisture (the amount of vapor in the case of wetting by steam) and the conductivity. 1 is when the insulator surface is moist to some extent, and 2 is when it is dry.
In this way, proper wetting varies depending on the wetness state of the insulator surface before wetting starts. For example, if the amount of adhering moisture is supplied in accordance with case 2, in case 1 there is a risk of contaminants dripping due to overwetting. Combined with case 2, the amount of wetting is insufficient and cannot be used as a measurement value, making it extremely difficult to achieve appropriate wetting according to various conditions. However, when we look at the change in conductivity with respect to the amount of adhered moisture, the change becomes smaller as it approaches proper moisture, and this trend is the same regardless of the wet state of the insulator before wetting begins. The present invention utilizes this to control the amount of wetting. That is, the amount or rate of change in the conductivity of the soiled material as the wetting progresses is detected, and when the change becomes less than a certain value, it is determined that proper wetting has been achieved, and the amount of wetting is controlled. Second
In the figure, 1' and 2' indicate changes in the rate of change in cases of 1 and 2, respectively. Due to this principle, it is possible to control the humidity to be appropriate according to the amount of contamination without being affected by the wet state of the insulator before measurement, the amount of contamination, or other factors.
第3図は本発明の制御方法の自動化を図るため
の実施例を示すブロツク図であり、3は電極、4
は電気抵抗検出器である。これにより電気抵抗は
電圧に変換される。5は起動用比較器で、電極が
湿潤し、付着汚損物が溶解し始めると電気抵抗が
徐々に高くなつていき検出器4の出力電圧が上昇
していくが、その出力がある値以上になつてから
制御回路を起動させるものである。7はその起動
電圧設定器を示す。6はタイミングパルス発生器
でたとえば数10secに1回数10msecのパルス幅の
照合パルスPc及びそのパルス終了により発生す
る数msecのサンプリングパルスPsを発生する。
このパルス周期の時間差による電圧の変化をとら
え湿潤量を制御しようとするものである。9は記
憶器でサンプリングパルスにより検出器4の出力
電圧を記憶する。このあと差動増幅器10で検出
器4と記憶器9の出力電圧の差を増幅し、比較器
11により制御する変化量によつて決まる規定値
との比較を行なう。12は掛算器で制御回路起動
がかかり変化量が規定値に達したという条件によ
り蒸気発生器13を停止させる。8はその規定値
設定器を示す。この制御回路により付着汚損物の
溶解が完了又はほぼ完了した状態でこれ以上の水
分の付着を停止でき、最初から湿潤していた場合
等の過度の湿潤による汚損物の滴下を防ぐ事がで
きる。 FIG. 3 is a block diagram showing an embodiment for automating the control method of the present invention.
is an electrical resistance detector. This converts electrical resistance into voltage. 5 is a starting comparator; when the electrode becomes wet and the attached contaminants begin to dissolve, the electrical resistance gradually increases and the output voltage of the detector 4 increases, but when the output exceeds a certain value This is to activate the control circuit after the temperature is reached. 7 shows the starting voltage setting device. Reference numeral 6 denotes a timing pulse generator which generates a verification pulse Pc with a pulse width of 10 msec once every several tens of seconds, and a sampling pulse Ps of several msec generated when the pulse ends.
This method attempts to control the amount of moisture by capturing changes in voltage due to the time difference in pulse periods. A memory 9 stores the output voltage of the detector 4 using sampling pulses. Thereafter, the differential amplifier 10 amplifies the difference between the output voltages of the detector 4 and the memory 9, and the comparator 11 compares the difference with a specified value determined by the amount of change controlled. Numeral 12 is a multiplier which activates the control circuit and stops the steam generator 13 on condition that the amount of change has reached a specified value. 8 indicates the specified value setting device. With this control circuit, further adhesion of moisture can be stopped when the dissolution of the adhered contaminants is completed or almost completed, and it is possible to prevent contaminants from dripping due to excessive moisture, such as when it is wet from the beginning.
以上の如く、本発明によれば碍子下面の湿潤量
を制御するという従来実施されていなかつたもの
を可能にしたばかりでなく、付着汚損物を溶解す
るのに必要な水分量を汚損物の量に応じて供給す
ることが可能であるという事で碍子汚損量測定の
性能向上に果す役割は非常に大きいものである。 As described above, the present invention not only makes it possible to control the amount of moisture on the lower surface of the insulator, which has not been done in the past, but also makes it possible to reduce the amount of moisture necessary to dissolve the adhered contaminants to the amount of contaminants. Since it can be supplied according to the requirements, it plays a very large role in improving the performance of measuring the amount of insulator contamination.
第1図は湿潤度と導電度の関係を示すグラフ、
第2図は付着水分量の変化に伴う導電度及び導電
度の変化率の変化を示すグラフ、第3図は本発明
方法の自動化を図る実施例を示すブロツク図であ
る。
Figure 1 is a graph showing the relationship between wetness and conductivity.
FIG. 2 is a graph showing changes in conductivity and the rate of change in conductivity with changes in the amount of adhering moisture, and FIG. 3 is a block diagram showing an example of automating the method of the present invention.
Claims (1)
を配置し、同碍子の下面に付着した汚損物の量を
測定する際に、水蒸気等を同碍子の下面に付着さ
せ、その水分によつて湿潤された汚損物の量の大
きさが上記電極間の導電度の大きさになつて表わ
れることを利用した湿潤式碍子汚損測定におい
て、湿潤開始から上記電極間の導電度を逐次検出
し、その導電度の変化率が所定の値以下になつた
時に湿潤動作を停止させることを特徴とする適正
湿潤量制御方法。1 An electrode for measuring the amount of contamination is placed on the underside of the pilot insulator, and when measuring the amount of contaminants adhering to the underside of the insulator, water vapor, etc. is attached to the underside of the insulator, and the moisture is used to moisten the insulator. In wet insulator stain measurement, which takes advantage of the fact that the amount of contaminants applied is expressed as the conductivity between the electrodes, the conductivity between the electrodes is sequentially detected from the start of wetting, and the conductivity between the electrodes is sequentially detected. A method for controlling an appropriate amount of wetting, characterized by stopping a wetting operation when a rate of change in conductivity falls below a predetermined value.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7649779A JPS561344A (en) | 1979-06-18 | 1979-06-18 | Controlling method for optimum wet-quantity in wet-type insulator stain measurement |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7649779A JPS561344A (en) | 1979-06-18 | 1979-06-18 | Controlling method for optimum wet-quantity in wet-type insulator stain measurement |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS561344A JPS561344A (en) | 1981-01-09 |
| JPS6130710B2 true JPS6130710B2 (en) | 1986-07-15 |
Family
ID=13606851
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7649779A Granted JPS561344A (en) | 1979-06-18 | 1979-06-18 | Controlling method for optimum wet-quantity in wet-type insulator stain measurement |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS561344A (en) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5646735A (en) * | 1979-09-25 | 1981-04-28 | Japan Styrene Paper Co Ltd | Freparation of polyolefin series resin foamed molding body |
| JPS5845032A (en) * | 1981-09-10 | 1983-03-16 | Japan Styrene Paper Co Ltd | Manufacture of synthetic resin foamed and molded item |
| JPS5855231A (en) * | 1981-09-28 | 1983-04-01 | Japan Styrene Paper Co Ltd | Manufacture of polyolefinic resin prefoamed particle |
| JPS5861128A (en) * | 1981-10-09 | 1983-04-12 | Asahi Chem Ind Co Ltd | Foamed molded propylene resin article and its preparation |
| JPS5865734A (en) * | 1981-10-14 | 1983-04-19 | Kanegafuchi Chem Ind Co Ltd | Foamed polypropylene resin particles and preparing same |
| JPS5876233A (en) * | 1981-11-02 | 1983-05-09 | Japan Styrene Paper Co Ltd | Manufacture of ethylene/propylene copolymer prefoamed particle |
| JPS5876231A (en) * | 1981-11-02 | 1983-05-09 | Japan Styrene Paper Co Ltd | Manufacture of polypropylene resin prefoamed particle |
| JPS5876227A (en) * | 1981-11-02 | 1983-05-09 | Japan Styrene Paper Co Ltd | Manufacture of polypropylene resin foamed and molded body |
| JPS5876232A (en) * | 1981-11-02 | 1983-05-09 | Japan Styrene Paper Co Ltd | Manufacture of polypropylene resin prefoamed particle |
| JPS6010047B2 (en) * | 1981-11-02 | 1985-03-14 | 日本スチレンペ−パ−株式会社 | Non-crosslinked linear low density polyethylene pre-expanded particles and method for producing the same |
| JPS58125729A (en) * | 1982-01-21 | 1983-07-26 | Japan Styrene Paper Co Ltd | Production of prefoamed particles |
| JPS58141218A (en) * | 1982-02-16 | 1983-08-22 | Japan Styrene Paper Co Ltd | Expanded polypropylene particle in-mold molding having easy cuttability |
| JPS58127633U (en) * | 1982-02-19 | 1983-08-30 | 松下電器産業株式会社 | porcelain capacitor |
| JPS58133413U (en) * | 1982-03-05 | 1983-09-08 | 日本スチレンペ−パ−株式会社 | Non-crosslinked polypropylene resin foam container |
| JPS58197028A (en) * | 1982-05-13 | 1983-11-16 | Kanegafuchi Chem Ind Co Ltd | Pre-foaming of thermoplastic resin granule |
| JPS58197027A (en) * | 1982-05-13 | 1983-11-16 | Kanegafuchi Chem Ind Co Ltd | Prefoaming of thermoplastic resin particles |
| JPS58213028A (en) * | 1982-06-04 | 1983-12-10 | Japan Styrene Paper Co Ltd | In-mold expansion polypropylene resin molding |
| JPS591923U (en) * | 1982-06-28 | 1984-01-07 | 株式会社小松製作所 | trunnion bearing |
| JPS5959730A (en) * | 1982-09-30 | 1984-04-05 | Japan Styrene Paper Co Ltd | Aggregate of polypropylene resin particle |
| JPS5962119A (en) * | 1982-10-01 | 1984-04-09 | Japan Styrene Paper Co Ltd | Polypropylene family resin foaming molded product |
| JPS5973826U (en) * | 1982-11-11 | 1984-05-19 | ティーディーケイ株式会社 | Filter module |
| JPS5976085U (en) * | 1982-11-15 | 1984-05-23 | ソニー株式会社 | connector |
| JPS59127734A (en) * | 1983-01-07 | 1984-07-23 | Japan Styrene Paper Co Ltd | Preparation of pre-expanded polymer particle |
| JPS59111823A (en) * | 1982-12-20 | 1984-06-28 | Japan Styrene Paper Co Ltd | Manufacture of preliminarily expanded polymer particle |
| JPS60245650A (en) * | 1984-05-21 | 1985-12-05 | Japan Styrene Paper Co Ltd | Preparation of foamed particle of noncrosslinked polypropylene resin |
| US4704239A (en) * | 1984-04-28 | 1987-11-03 | Japan Styrene Paper Corp. | Process for the production of expanded particles of a polymeric material |
| JPS60235849A (en) * | 1984-05-08 | 1985-11-22 | Japan Styrene Paper Co Ltd | Prefoamed particle of polypropylene resin |
| JPS61192524A (en) * | 1985-02-20 | 1986-08-27 | Sekisui Plastics Co Ltd | Prefoaming of expandable thermoplastic resin particle |
| US4778829A (en) * | 1985-07-12 | 1988-10-18 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Process for preparing pre-expanded particles of thermoplastic resin |
| JPH082989B2 (en) | 1987-05-11 | 1996-01-17 | 日本スチレンペ−パ−株式会社 | Pre-expansion method of polyolefin resin particles |
| JP2666061B2 (en) * | 1987-09-04 | 1997-10-22 | 株式会社ジェイ エス ピー | Pre-expansion method of polyolefin resin particles |
| EP0495125B1 (en) * | 1990-08-06 | 1996-11-27 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Foam-molded item of olefinic synthetic resin and method of manufacturing the same |
| JP4888901B2 (en) * | 2007-03-16 | 2012-02-29 | 公益財団法人鉄道総合技術研究所 | Deterioration state measuring device and deterioration state measuring method |
-
1979
- 1979-06-18 JP JP7649779A patent/JPS561344A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS561344A (en) | 1981-01-09 |
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