JPH10213578A - Water quality analyzer - Google Patents

Water quality analyzer

Info

Publication number
JPH10213578A
JPH10213578A JP3125097A JP3125097A JPH10213578A JP H10213578 A JPH10213578 A JP H10213578A JP 3125097 A JP3125097 A JP 3125097A JP 3125097 A JP3125097 A JP 3125097A JP H10213578 A JPH10213578 A JP H10213578A
Authority
JP
Japan
Prior art keywords
meter
unit
sample
carrier gas
reaction tube
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
Application number
JP3125097A
Other languages
Japanese (ja)
Inventor
Kenji Iharada
健志 居原田
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.)
Shimadzu Corp
Original Assignee
Shimadzu 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 Shimadzu Corp filed Critical Shimadzu Corp
Priority to JP3125097A priority Critical patent/JPH10213578A/en
Publication of JPH10213578A publication Critical patent/JPH10213578A/en
Pending legal-status Critical Current

Links

Landscapes

  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)

Abstract

PROBLEM TO BE SOLVED: To increase measurement sensitivity to nitrogen in a water quality analyzer in which both TOC and TN in a water solution specimen can be measured by one analyzer. SOLUTION: An oxidation catalyst 4 in a reaction tube 6 is heated to a specified temperature of 680 to 900 deg.C by an electric furnace 8, and refining air is fed as carrier gas from a flow control part 12 to the reaction tube 6 at a flow rate of 150ml/min. Under the conditions, a water solution specimen of 100μl is sampled by a specimen sampling part 10, and filled into the reaction tube 6. Also the specimen gas vaporized in the reaction tube 6 is fed through a dehumidifying part 14 to the CO2 meter 16 of an NDIR (Non-dispersion type infrared spectrophotometer) by the carrier gas, and the CO2 density is measured. Then it is fed to a chemical luminous type NO meter 18, and NO density is measured.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は1台の分析装置で水
溶液試料中のTOC(全有機体炭素)とTN(全窒素)
をともに測定できる水質分析計に関するものである。そ
のような水質分析計は、水溶液試料を接触熱分解して気
化するとともに、試料中の全窒素をNOに、全炭素をC
2に変換する酸化反応部、水溶液試料の一定量を採取
してその酸化反応部に注入する試料サンプリング部、そ
の酸化反応部にキャリアガスを供給するキャリアガス供
給部、酸化反応部からキャリアガスとともに送られてき
た試料気化ガス中のNOを検出するNO検出部、及びそ
の試料気化ガス中のCO2を検出するCO2検出部を備え
ている。そのような水質分析計は、下水や河川水に含ま
れる汚濁成分をモニタするTOCモニタやTNモニタと
して利用されたり、環境基準が設けられている海域や排
水基準が設けられている工場などでの水質監視用などに
利用されている。
TECHNICAL FIELD The present invention relates to a method for analyzing TOC (total organic carbon) and TN (total nitrogen) in an aqueous solution sample using a single analyzer.
And a water quality analyzer that can measure both. Such a water quality analyzer vaporizes an aqueous solution sample by catalytic pyrolysis, and converts all nitrogen in the sample to NO and all carbon to C
An oxidation reaction section for converting to O 2 , a sample sampling section for collecting a certain amount of an aqueous solution sample and injecting it into the oxidation reaction section, a carrier gas supply section for supplying a carrier gas to the oxidation reaction section, and a carrier gas from the oxidation reaction section A NO detection unit for detecting NO in the sample vaporized gas sent together with the gas and a CO 2 detection unit for detecting CO 2 in the sample vaporized gas are provided. Such a water quality analyzer is used as a TOC monitor or a TN monitor for monitoring pollutants contained in sewage and river water, and is used in sea areas where environmental standards are established or in factories where wastewater standards are established. It is used for monitoring water quality.

【0002】[0002]

【従来の技術】TOCのみを測定するTOC計は、検出
部として非分散型赤外分光光度計(NDIR)を利用し
た非分散型赤外線CO2計が用いられている。TNのみ
を測定するTN計は、検出部としてオゾン発生部を備え
てそのオゾン発生部から供給されたオゾンとNOとの反
応による発光を測定する化学発光式NO計、又はCO2
計と同様にNDIRを利用した非分散型赤外線NO計が
用いられている。
2. Description of the Related Art A non-dispersive infrared CO 2 meter using a non-dispersive infrared spectrophotometer (NDIR) is used as a detection unit in a TOC meter for measuring only TOC. A TN meter that measures only TN includes a chemiluminescence NO meter that includes an ozone generation unit as a detection unit and measures light emission due to the reaction between NO and ozone supplied from the ozone generation unit, or CO 2
A non-dispersive infrared NO meter using NDIR is used in the same manner as the meter.

【0003】しかし、1台の分析装置でTOCとTNを
ともに測定できるようにした水質分析計は、その検出部
としてCO2計もNO計もともにNDIRが使用されて
いる。これは、NDIRは同じ装置であっても、フィル
タセルに封入するガスの種類を異ならせることにより、
異なる成分ガスを測定できるという汎用性を備えている
からであり、装置も簡単であるからである。
[0003] However, in a water quality analyzer in which both TOC and TN can be measured by one analyzer, both the CO 2 meter and the NO meter use NDIR as a detection unit. This is because even if the NDIR is the same device, the type of gas sealed in the filter cell is different,
This is because it has versatility that different component gases can be measured, and the apparatus is simple.

【0004】[0004]

【発明が解決しようとする課題】NO計としてNDIR
を使用すると、窒素に対する測定感度が不十分であるこ
とがわかった。そこで、本発明は1台の分析装置で水溶
液試料中のTOCとTNをともに測定できる水質分析計
において、窒素に対する測定感度を向上させることを目
的とするものである。
Problems to be Solved by the Invention NDIR as NO meter
Was found to be insufficient in measurement sensitivity to nitrogen. Accordingly, an object of the present invention is to improve the measurement sensitivity to nitrogen in a water quality analyzer capable of measuring both TOC and TN in an aqueous solution sample with one analyzer.

【0005】[0005]

【課題を解決するための手段】本発明では、NO検出部
としてオゾン発生部を備えてそのオゾン発生部から供給
されたオゾンとNOとの反応による発光を測定する化学
発光式(ケミルミネッセンス式、略してケミルミ式又は
CL式ともいう)NO計を用い、CO2検出部としては
従来と同様に非分散型赤外線CO2計を用いる。NO検
出に関してはNDIRよりも化学発光式NO計の方が高
感度に測定することができる。
According to the present invention, a chemiluminescence type (chemiluminescence type) is provided which includes an ozone generator as an NO detector and measures light emission due to the reaction between ozone and NO supplied from the ozone generator. A NO meter is used as the CO 2 detection unit, and a non-dispersive infrared CO 2 meter is used as in the related art. Regarding NO detection, a chemiluminescent NO meter can measure with higher sensitivity than NDIR.

【0006】[0006]

【実施例】図1は一実施例を概略的に表わしたものであ
る。2は酸化反応部であり、金属酸化物や貴金属触媒の
酸化触媒4が充填された石英ガラス製反応管6が電気炉
8により所定の温度に加熱されるようになっている。試
料サンプリング部10により一定量の水溶液試料が採取
されて、反応管6に上部から注入される。反応管6に注
入された水溶液試料は、加熱された酸化触媒4と接触し
て熱分解し気化するとともに、試料中の窒素成分がNO
に変換され、同時に炭素成分がCO2に変換される。反
応管6の上部からは炭素分を除去した精製空気が流量制
御部12により一定流量に制御されてキャリアガスとし
て供給される。
FIG. 1 schematically shows an embodiment. Reference numeral 2 denotes an oxidation reaction section, and a quartz glass reaction tube 6 filled with an oxidation catalyst 4 of a metal oxide or a noble metal catalyst is heated to a predetermined temperature by an electric furnace 8. A certain amount of the aqueous solution sample is collected by the sample sampling unit 10 and injected into the reaction tube 6 from above. The aqueous solution sample injected into the reaction tube 6 comes into contact with the heated oxidation catalyst 4 to be thermally decomposed and vaporized, and the nitrogen component in the sample becomes NO.
And at the same time the carbon component is converted to CO 2 . From the upper part of the reaction tube 6, purified air from which the carbon content has been removed is controlled as a constant flow rate by the flow rate control unit 12 and supplied as a carrier gas.

【0007】反応管6で気化した試料ガスがキャリアガ
スにより送られ、除湿部を経てCO2検出器としての非
分散型赤外線CO2計16に導かれてCO2濃度が測定さ
れる。CO2計16を通過した試料ガスは、化学発光式
NO計18へ導かれ、その試料ガス中のNOがオゾン発
生部20から供給されるオゾンと反応することによって
発生する化学発光が検出されてNO濃度が測定される。
NO計18を通過した試料ガスはオゾン分解部を経て放
出される。オゾン発生部20は空気を原料とするもので
あるが、その原料としては炭素分を除去した精製空気が
流量制御部12により一定流量に制御されて供給され
る。
[0007] The sample gas vaporized in the reaction tube 6 is sent by a carrier gas, guided to a non-dispersive infrared CO 2 meter 16 as a CO 2 detector through a dehumidifying section, and the CO 2 concentration is measured. The sample gas that has passed through the CO 2 meter 16 is led to a chemiluminescence type NO meter 18, where chemiluminescence generated by the reaction of NO in the sample gas with ozone supplied from the ozone generator 20 is detected. The NO concentration is measured.
The sample gas that has passed through the NO meter 18 is released through an ozone decomposition unit. The ozone generator 20 uses air as a raw material. As the raw material, purified air from which carbon has been removed is supplied at a constant flow rate controlled by the flow rate control unit 12.

【0008】非分散型赤外線CO2計16と化学発光式
NO計18の検出出力は、それぞれデータ処理部22で
処理されてCO2とNOの濃度がそれぞれ求められ、プ
リンタやCRTなどの出力部24に出力される。データ
処理部22は非分散型赤外線CO2計16と化学発光式
NO計18の検出出力を増幅するアナログ増幅器、その
増幅された出力をデジタル信号に変換するA/D変換
器、及びその変換されたデジタル信号からCO2とNO
の濃度を算出するCPUなどを含んでいる。
The detection outputs of the non-dispersive infrared CO 2 meter 16 and the chemiluminescence NO meter 18 are respectively processed by a data processing section 22 to obtain the concentrations of CO 2 and NO, respectively. 24. The data processing unit 22 is an analog amplifier for amplifying the detection output of the non-dispersive infrared CO 2 meter 16 and the chemiluminescence NO meter 18, an A / D converter for converting the amplified output to a digital signal, and the converted signal. CO 2 and NO from the digital signal
And the like for calculating the density of the image.

【0009】次に、この実施例の動作を説明する。電気
炉8により反応管6中の酸化触媒4を680〜900℃
の所定の温度に加熱しておき、流量制御部12からキャ
リアガスとして精製空気を150ml/分の流量で反応
管6に供給しておく。その状態で、試料サンプリング部
10により100μlの水溶液試料を採取して反応管6
に注入する。反応管6で気化した試料ガスがキャリアガ
スにより送られ、除湿部14を経てCO2計16に導か
れてCO2濃度が測定され、その後NO計18へ導かれ
てNO濃度が測定される。
Next, the operation of this embodiment will be described. The oxidation catalyst 4 in the reaction tube 6 is heated to 680 to 900 ° C. by the electric furnace 8.
, And purified air is supplied as a carrier gas from the flow controller 12 to the reaction tube 6 at a flow rate of 150 ml / min. In this state, a 100 μl aqueous solution sample was collected by the sample
Inject into The sample gas vaporized in the reaction tube 6 is sent by a carrier gas, passed through the dehumidifying section 14 to the CO 2 meter 16 to measure the CO 2 concentration, and then to the NO meter 18 to measure the NO concentration.

【0010】図1の実施例ではCO2計16とNO計1
8は直列に接続されているので、反応管6で気化した試
料ガスがCO2計16を経てNO計18に導かれ、同じ
試料ガスがCO2計16とNO計18の両方で測定され
る。
In the embodiment shown in FIG. 1, the CO 2 total 16 and the NO total 1
Since 8 is connected in series, the sample gas vaporized in the reaction tube 6 is led to the NO meter 18 via the CO 2 meter 16, and the same sample gas is measured by both the CO 2 meter 16 and the NO meter 18. .

【0011】図2はCO2計16とNO計18の他の配
列の例を示したものである。図2では、反応管6で気化
した試料ガスがキャリアガスにより送られ、除湿部14
を経て切換え部26によりCO2計16とNO計18に
切り換えて導かれる。
FIG. 2 shows an example of another arrangement of the CO 2 meter 16 and the NO meter 18. In FIG. 2, the sample gas vaporized in the reaction tube 6 is sent by the carrier gas, and
After that, the switching unit 26 switches between the CO 2 meter 16 and the NO meter 18 and guides them.

【0012】[0012]

【発明の効果】本発明では、1台の分析装置で水溶液試
料中のTOCとTNをともに測定できる水質分析計にお
いて、NO検出部として化学発光式NO計を用いるよう
にしたので、CO2検出部もNO検出部もともにNDI
Rを使用している従来の分析計に比べると、窒素量測定
感度が向上する。
According to the present invention, in a water quality analyzer capable of measuring both TOC and TN in an aqueous solution sample with a single analyzer, a chemiluminescent NO meter is used as the NO detecting portion, so that CO 2 can be detected. And NO detector are both NDI
Compared with the conventional analyzer using R, the sensitivity of measuring the amount of nitrogen is improved.

【図面の簡単な説明】[Brief description of the drawings]

【図1】一実施例を概略的に示すブロック図である。FIG. 1 is a block diagram schematically showing one embodiment.

【図2】CO2計とNO計の他の配列例を示すブロック
図である。
FIG. 2 is a block diagram showing another arrangement example of the CO 2 meter and the NO meter.

【符号の説明】[Explanation of symbols]

2 酸化反応部 4 酸化触媒 6 反応管 8 電気炉 10 試料サンプリング部 12 流量制御部 16 非分散型赤外線CO2計 18 化学発光式NO計 20 オゾン発生部 22 データ処理部2 Oxidation reaction unit 4 Oxidation catalyst 6 Reaction tube 8 Electric furnace 10 Sample sampling unit 12 Flow control unit 16 Non-dispersive infrared CO 2 meter 18 Chemiluminescence NO meter 20 Ozone generation unit 22 Data processing unit

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 水溶液試料を熱分解して気化するととも
に、試料中の全窒素をNOに、全炭素をCO2に変換す
る酸化反応部、水溶液試料の一定量を採取して前記酸化
反応部に注入する試料サンプリング部、前記酸化反応部
にキャリアガスを供給するキャリアガス供給部、前記酸
化反応部からキャリアガスとともに送られてきた試料気
化ガス中のNOを検出するNO検出部、及びその試料気
化ガス中のCO2を検出するCO2検出部を備えた水質分
析計において、 前記NO検出部はオゾン発生部を備えてそのオゾン発生
部から供給されたオゾンとNOとの反応による発光を測
定する化学発光式NO計であり、 前記CO2検出部は非分散型赤外線CO2計であることを
特徴とする水質分析計。
An oxidation reaction section for thermally decomposing and vaporizing an aqueous solution sample, converting all the nitrogen in the sample to NO and converting all carbon to CO 2 , and collecting a certain amount of the aqueous solution sample to obtain the oxidation reaction section A sample sampling unit for injecting the carrier gas to the oxidation reaction unit, a carrier gas supply unit for supplying a carrier gas to the oxidation reaction unit, a NO detection unit for detecting NO in the sample vaporized gas sent together with the carrier gas from the oxidation reaction unit, and a sample thereof. In a water quality analyzer provided with a CO 2 detecting unit for detecting CO 2 in a vaporized gas, the NO detecting unit includes an ozone generating unit and measures light emission due to a reaction between ozone supplied from the ozone generating unit and NO. A water quality analyzer, wherein the CO 2 detection unit is a non-dispersive infrared CO 2 meter.
JP3125097A 1997-01-29 1997-01-29 Water quality analyzer Pending JPH10213578A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3125097A JPH10213578A (en) 1997-01-29 1997-01-29 Water quality analyzer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3125097A JPH10213578A (en) 1997-01-29 1997-01-29 Water quality analyzer

Publications (1)

Publication Number Publication Date
JPH10213578A true JPH10213578A (en) 1998-08-11

Family

ID=12326128

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3125097A Pending JPH10213578A (en) 1997-01-29 1997-01-29 Water quality analyzer

Country Status (1)

Country Link
JP (1) JPH10213578A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20010090641A (en) * 2000-04-10 2001-10-19 손정익 Infrared CO2 analyzing system using sample injection method
EP1243917A1 (en) * 2001-03-23 2002-09-25 Instrumentarium Corporation Nitric oxide analyzer

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20010090641A (en) * 2000-04-10 2001-10-19 손정익 Infrared CO2 analyzing system using sample injection method
EP1243917A1 (en) * 2001-03-23 2002-09-25 Instrumentarium Corporation Nitric oxide analyzer

Similar Documents

Publication Publication Date Title
EP0670490A3 (en) Method and apparatus for measuring a gaseous medium with a chemical sensor.
US3659100A (en) System and method of air pollution monitoring utilizing chemiluminescence reactions
WO2002033393A3 (en) Method and apparatus for analyzing mixtures of gases
US4332591A (en) Analytical method and apparatus for the determination of total nitrogen contents in aqueous systems
US3652227A (en) Nitric oxide analysis
US4077774A (en) Interferent-free fluorescence detection of sulfur dioxide
US3464797A (en) Instrument for determining ozone
CA2429854A1 (en) A method for measuring the total concentration of carbon monoxide and hydrocarbons in oxygen by means of ion mobility spectrometry
JPH10213578A (en) Water quality analyzer
JP4314737B2 (en) Chemiluminescent nitrogen oxide concentration meter
JP2008261865A (en) Instrument for measuring volatile organic compound
JPH1151869A (en) Total organic carbon/total nitrogen meter
US20030162305A1 (en) Gas contaminant detection and quantification method
WO1993011421A1 (en) Method and apparatus for monitoring a supply of gas
Kondrat’Eva et al. Comparative study of gas-analyzing systems designed for continuous monitoring of TPP emissions
JP2004138467A (en) Ultraviolet absorption type measuring instrument and method for treating measurement specimen
JP3777786B2 (en) Total nitrogen meter
JPH11125629A (en) Water quality analyzer
SU1713882A1 (en) Method of measuring hydrogen concentration
JP3111647B2 (en) Carbon content measuring device
JP2855830B2 (en) Moisture and total organic carbon analyzer
JPH0546500B2 (en)
JP3113931U (en) Volatile organic compound measuring device
RU38945U1 (en) ANALYZER OF SELECTIVE DETERMINATION OF VOLUME HYDROGEN CONCENTRATION IN GASES
JPH10213548A (en) Chemiluminescence type nitrogen oxide measuring device