JP2005062136A - Mustard detector - Google Patents
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- JP2005062136A JP2005062136A JP2003296433A JP2003296433A JP2005062136A JP 2005062136 A JP2005062136 A JP 2005062136A JP 2003296433 A JP2003296433 A JP 2003296433A JP 2003296433 A JP2003296433 A JP 2003296433A JP 2005062136 A JP2005062136 A JP 2005062136A
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Abstract
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本発明は、びらん性毒ガスの一種であるマスタードを検出する装置に関する。 The present invention relates to an apparatus for detecting mustard which is a kind of erosive poison gas.
テロなどの犯罪に使用されるびらん性毒ガスは、程度の極めて低い濃度で人体など生物に重篤な影響を与えるため、高い感度と選択性で、しかも可及的速やかに検出し、対策を施すことが必要となる。
すなわち、原因が分からないまま事態が進展すれば被害が拡大し人命は失われていく。一刻も早く中毒を引き起こす原因物質(中毒起因物質)が何であるかつきとめなければならない。被害者の診断による症状の情報のみからでは、適切な治療は行えない。毒の種類がわかれば解毒薬投与、処置等いくらでも対策が立てられる。極めて低濃度のびらん性毒ガスなどは、クロマトグラフ装置など実験室レベルで使用可能な分析機器により正確に検出できるものの、犯罪現場での使用は困難である。
Erosive toxic gases used in crimes such as terrorism have serious effects on living organisms, such as the human body, at extremely low concentrations. Therefore, they are detected with high sensitivity and selectivity and as soon as possible. It will be necessary.
In other words, if the situation progresses without knowing the cause, the damage will expand and human lives will be lost. It must be determined what is the causative substance (toxic substance) that causes poisoning as soon as possible. Appropriate treatment cannot be performed only from information on the symptoms of the victim's diagnosis. If you know the type of poison, you can take as many measures as possible, including the administration of antidote and treatment. An extremely low concentration of erosive poisoning gas can be accurately detected by an analytical instrument that can be used at the laboratory level, such as a chromatograph, but it is difficult to use in crime scenes.
このような0.1mg/立方メートル程度の極めて濃度の低い毒ガスの検出は、ガスクロマトー質量分析装置など実験室レベルでは実用的な分析機器により簡単に検出できるものの、犯罪現場での使用は困難である。
このため、各種ガスセンサーや検知管等の現場で容易に使用できる検出手段の応用が検討されているが、未だ実用に供するのに十分な感度を引き出すまでには至っておらず、現実には現場に毒ガスが存在するか否かを判定するため、カナリアをセンサーとして使用されたこともあったが、濃度や種類、分布状況など、対策に必要となるデータを得ることはとても不可能である。
Although detection of such a poison gas with a very low concentration of about 0.1 mg / cubic meter can be easily detected by a practical analytical instrument such as a gas chromatograph mass spectrometer at a laboratory level, it is difficult to use in a crime scene. .
For this reason, the application of detection means that can be easily used in the field, such as various gas sensors and detector tubes, has been studied, but it has not yet reached a sufficient sensitivity for practical use. In order to determine whether or not poisonous gas exists, canary was used as a sensor, but it is very impossible to obtain data necessary for countermeasures such as concentration, type, and distribution status.
本発明はこのような事情に鑑みてなされたものであって、生物に影響を与える濃度が0.1mg/立方メートル程度のマスタードをフィールドで簡単に検出することができる新規なマスタード検出装置を提供することである。 The present invention has been made in view of such circumstances, and provides a novel mustard detection apparatus capable of easily detecting in the field a mustard having a concentration of about 0.1 mg / cubic meter that affects living organisms. That is.
このような問題を解消するために本発明においては、温度300℃以上に被検ガスを加熱する熱分解炉と、前記熱分解炉からのガスを検出する検知材と、前記検知材の光学濃度を検出する光学濃度検知手段とを備え、前記検知材が、水素イオン指示薬及び保湿剤を担体に展開して構成されている。 In order to solve such a problem, in the present invention, a pyrolysis furnace that heats a test gas to a temperature of 300 ° C. or higher, a detection material that detects gas from the pyrolysis furnace, and an optical density of the detection material And an optical density detection means for detecting the above, and the detection material is constituted by developing a hydrogen ion indicator and a humectant on a carrier.
マスタードを温度300℃に加熱して塩酸を発生させ、これを検知材に反応させて光学濃度の変化として検出できるため、特別な分析技術や設備を必要とすることなく、フィールドでの使用が可能となる。
また、サンプリング時間を変更するだけで、同一の装置で緊急性を重視した検出と精度を重視した検出とに対応することができる。
The mustard is heated to a temperature of 300 ° C to generate hydrochloric acid, which can be detected as a change in optical density by reacting with a detection material, so that it can be used in the field without the need for special analysis techniques or equipment. It becomes.
In addition, by simply changing the sampling time, it is possible to cope with detection that emphasizes urgency and detection that emphasizes accuracy with the same apparatus.
そこで以下に本発明の詳細を図示した実施例に基づいて説明する。
図1は、本発明の一実施例を示すものであって、熱分解炉1は、流入口2aがサンプリング領域に接続される反応管2にヒータ3を巻回して構成され、流出口2bが後述する検出手段10の測定ヘッドに接続されている。
Therefore, details of the present invention will be described below based on the illustrated embodiment.
FIG. 1 shows an embodiment of the present invention. A pyrolysis furnace 1 is configured by winding a heater 3 around a
検出手段10は、検知材Sを、発光素子11と受光素子12とを備えた光学濃度検知手段としての測定ヘッド13に、一定時間毎に搬送するテープ搬送機構14と、サンプリングポンプ15からの負圧を受けて、測定ヘッド13と共同して検知材Sに被検ガスを接触させる吸引ヘッド16とから構成されている。なお、図中符号17は、検知材Sの未使用領域を測定領域に一定量送り出すための間欠駆動部を示す。
The detecting means 10 includes a tape conveying mechanism 14 for conveying the detection material S to a
ところで検知材Sは、水素イオン濃度指示薬、例えばメチルレッド0.22wt%、バッファ溶液17.5ミリリットル、及び保湿剤、例えばグリセリンやエチレングリコール等の多価アルコール15mlを、全量が100mlとなるようにメタノール等の易蒸発性有機溶媒に溶解した発色液に、セルロースを素材とするろ紙に含浸させ有機溶媒を揮散させて構成されている。 By the way, the detection material S has a hydrogen ion concentration indicator, for example, methyl red 0.22 wt%, a buffer solution 17.5 ml, and a moisturizing agent, for example, 15 ml of polyhydric alcohol such as glycerin or ethylene glycol, so that the total amount becomes 100 ml. It is configured by impregnating a filter paper made of cellulose into a coloring solution dissolved in an easily evaporable organic solvent such as methanol and volatilizing the organic solvent.
なお、水素イオン指示薬としては、メチルオレンジのほか、メタニールイエロー、アザリンイエロー、ベンジルイエロー、メチルイエロー、メチールレッド、ベンジルオレンジ、トロペオリン、ブロモフェノールブルーを使用することが出来る。 In addition to methyl orange, methanol yellow, azaline yellow, benzyl yellow, methyl yellow, methyl red, benzyl orange, tropeoline, and bromophenol blue can be used as the hydrogen ion indicator.
この検知材Sは、テープ状に裁断してカセットケースに収容して連続測定用に供したり、また紙片に成形して遮気性の袋に保管し、必要の都度、遮気性袋から取り出してバッチ測定に供したりすることができる。 This detection material S is cut into a tape shape and housed in a cassette case for continuous measurement, or formed into a piece of paper and stored in an airtight bag, and taken out from the airtight bag whenever necessary and batched. It can be used for measurement.
この実施例において、吸引ヘッド16を引き下げて測定ヘッド13との間に検知材Sを挿入し、再び吸引ヘッド16を上昇させて測定ヘッド13に対向する領域にサンプリングポンプ15の吸引圧が作用するようにセットする。
In this embodiment, the
ついで、熱分解炉1の温度を500℃程度に維持し、濃度0.1mg/立方メートル程度のマスタードを含むエアを時間30秒だけ吸引すると、マスタードは熱分解炉1により塩酸を生成し、検知材Sの一方の面から他方の面に通過し、検知材Sに担持されている発色剤と反応する。この際、検知材のシリカゲルや保湿剤が反応を促進することになる。 Next, when the temperature of the pyrolysis furnace 1 is maintained at about 500 ° C. and air containing mustard with a concentration of about 0.1 mg / cubic meter is sucked for 30 seconds, the mustard generates hydrochloric acid by the pyrolysis furnace 1 and the detection material It passes from one surface of S to the other surface and reacts with the color former carried on the detection material S. At this time, silica gel or a humectant serving as a detection material accelerates the reaction.
このようにしてサンプリング時間が経過した時点で、測定ヘッド13の発光素子11と受光素子12とにより、ガスを通過させる以前の光学濃度との差分を検出すると、図2に示したように発色液の光学的飽和濃度の27%程度の検出出力を得ることができた。
When the sampling time elapses in this way and the difference between the optical density before the gas is passed is detected by the light emitting element 11 and the
もとより、熱分解炉1、及び検出手段10を駆動できるに足る電源を商用電源や、バッテリから供給するだけで、特別な分析技術を必要とすることなく、極めて低い濃度のマスタードを検出できるから、犯罪現場などのフィールドで使用可能となる。 Of course, it is possible to detect a mustard having an extremely low concentration without requiring a special analysis technique by simply supplying a power source sufficient to drive the pyrolysis furnace 1 and the detection means 10 from a commercial power source or a battery. It can be used in crime scenes and other fields.
なお、上述の実施例においては、サンプリング時間を30秒としたが、緊急性と検出感度との兼ね合いで、緊急性を要する場合には光学濃度の変化が検出できる程度に短縮し、またマスタードの濃度を正確に知る必要がある場合には延長するなど、サンプリング時間を適宜変更すると、用途に合った検出が可能となる。 In the above-described embodiment, the sampling time is set to 30 seconds. However, the balance between the urgency and the detection sensitivity is shortened to such an extent that the change in optical density can be detected when urgency is required. If the sampling time is appropriately changed, such as extending the concentration when it is necessary to know the concentration accurately, detection suitable for the application becomes possible.
上述の実施例においては熱分解炉1の温度を500℃に設定しているが、図2に示したように300℃以上であれば検出することが可能であり、また上限の温度は、感度の増加率とエネルギとの関係から700℃程度に制限するのが望ましい。 In the above-described embodiment, the temperature of the pyrolysis furnace 1 is set to 500 ° C., but as shown in FIG. 2, it can be detected if it is 300 ° C. or higher, and the upper limit temperature is the sensitivity. It is desirable to limit to about 700 ° C. from the relationship between the rate of increase in energy and energy.
1 熱分解炉 10 検出手段 13 測定ヘッド S 検知材 1 Pyrolysis furnace 10 Detection means 13 Measuring head S Detection material
Claims (2)
前記検知材が、水素イオン指示薬及び保湿剤を担体に展開して構成されているマスタード検出装置。 A pyrolysis furnace for heating the test gas to a temperature of 300 ° C. or higher, a detection material for detecting the gas from the pyrolysis furnace, and an optical density detection means for detecting the optical density of the detection material,
A mustard detection device in which the detection material is configured by developing a hydrogen ion indicator and a humectant on a carrier.
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JP2003296433A JP4225545B2 (en) | 2003-08-20 | 2003-08-20 | Mustard detection device |
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JP2003296433A JP4225545B2 (en) | 2003-08-20 | 2003-08-20 | Mustard detection device |
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JP4225545B2 JP4225545B2 (en) | 2009-02-18 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006284285A (en) * | 2005-03-31 | 2006-10-19 | Riken Keiki Co Ltd | Mustard detection device |
JP2007040934A (en) * | 2005-08-05 | 2007-02-15 | Riken Keiki Co Ltd | Agent for detecting organic-phosphorus-based nerve gas |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH0772138A (en) * | 1993-06-25 | 1995-03-17 | Riken Keiki Co Ltd | Acid gas detection paper |
JPH09117735A (en) * | 1995-10-26 | 1997-05-06 | Masatoshi Ishikawa | Decomposing treatment of organic hetero compound such as poison gas by hydrothermal action |
JP2001215221A (en) * | 2000-02-02 | 2001-08-10 | Air Liquide Japan Ltd | Reagent and method for detecting halide |
JP2001324491A (en) * | 2000-05-17 | 2001-11-22 | Riken Keiki Co Ltd | Octafluorocylopentene-measuring apparatus |
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0772138A (en) * | 1993-06-25 | 1995-03-17 | Riken Keiki Co Ltd | Acid gas detection paper |
JPH09117735A (en) * | 1995-10-26 | 1997-05-06 | Masatoshi Ishikawa | Decomposing treatment of organic hetero compound such as poison gas by hydrothermal action |
JP2001215221A (en) * | 2000-02-02 | 2001-08-10 | Air Liquide Japan Ltd | Reagent and method for detecting halide |
JP2001324491A (en) * | 2000-05-17 | 2001-11-22 | Riken Keiki Co Ltd | Octafluorocylopentene-measuring apparatus |
Non-Patent Citations (1)
Title |
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GLUKHOVTSEV, M.N. ET AL.: "A high-level computational study on the thermochemistry and thermal decomposition of sulfur mustard(", J. PHYS. CHEM. A, vol. 102, JPN6008011089, 1998, pages 3438 - 3446, ISSN: 0000996337 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006284285A (en) * | 2005-03-31 | 2006-10-19 | Riken Keiki Co Ltd | Mustard detection device |
JP4640944B2 (en) * | 2005-03-31 | 2011-03-02 | 理研計器株式会社 | Mustard detection device |
JP2007040934A (en) * | 2005-08-05 | 2007-02-15 | Riken Keiki Co Ltd | Agent for detecting organic-phosphorus-based nerve gas |
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