WO2013121577A1 - 全窒素測定装置 - Google Patents
全窒素測定装置 Download PDFInfo
- Publication number
- WO2013121577A1 WO2013121577A1 PCT/JP2012/053790 JP2012053790W WO2013121577A1 WO 2013121577 A1 WO2013121577 A1 WO 2013121577A1 JP 2012053790 W JP2012053790 W JP 2012053790W WO 2013121577 A1 WO2013121577 A1 WO 2013121577A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- total nitrogen
- ultraviolet lamp
- sample water
- sample
- nitrogen
- Prior art date
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title claims description 64
- 229910052757 nitrogen Inorganic materials 0.000 title claims description 32
- 238000005259 measurement Methods 0.000 title description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 35
- 229910052742 iron Inorganic materials 0.000 claims abstract description 20
- 239000000463 material Substances 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 36
- -1 nitrate ions Chemical class 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 17
- 229910017464 nitrogen compound Inorganic materials 0.000 claims description 17
- 150000002830 nitrogen compounds Chemical group 0.000 claims description 17
- 229910002651 NO3 Inorganic materials 0.000 claims description 12
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 238000002835 absorbance Methods 0.000 claims description 8
- 238000006864 oxidative decomposition reaction Methods 0.000 claims description 8
- 239000003153 chemical reaction reagent Substances 0.000 claims description 5
- 230000001678 irradiating effect Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 abstract description 14
- 239000000945 filler Substances 0.000 abstract description 5
- 238000000034 method Methods 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229910052710 silicon Inorganic materials 0.000 description 9
- 239000010703 silicon Substances 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 230000001590 oxidative effect Effects 0.000 description 5
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 229920002449 FKM Polymers 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 238000011481 absorbance measurement Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229920006333 epoxy cement Polymers 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- VLAPMBHFAWRUQP-UHFFFAOYSA-L molybdic acid Chemical compound O[Mo](O)(=O)=O VLAPMBHFAWRUQP-UHFFFAOYSA-L 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/33—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using ultraviolet light
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/631—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited using photolysis and investigating photolysed fragments
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
- G01N31/005—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods investigating the presence of an element by oxidation
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/18—Water
- G01N33/188—Determining the state of nitrification
Definitions
- the present invention includes a reaction vessel having a space for accommodating a sample in a space around the ultraviolet lamp, in which a light emitting portion of the ultraviolet lamp is inserted, and for oxidizing and decomposing nitrogen compounds in the reaction vessel
- the sample water to which the reaction reagent is added is stored and the sample water is irradiated with ultraviolet light from an ultraviolet lamp to oxidatively decompose the nitrogen compound, and the absorbance of the sample water after the nitrogen compound is oxidatively decomposed is measured.
- the present invention relates to a total nitrogen measuring device for measuring the concentration of nitrogen compounds contained in a sample.
- the “ultraviolet absorption method” defined in “Testing method of wastewater discharged from factories” of Japanese Industrial Standard is generally used.
- alkaline potassium peroxodisulfate which is an oxidant
- the nitrogen compound is thermally decomposed to nitrate ions at high temperature and pressure, and then the total nitrogen concentration is quantified by measuring the absorbance at 220 nm. It is.
- a measuring apparatus employing this method is required to have pressure resistance and heat resistance, it is necessary to make the material and design special.
- “An ultraviolet oxidative decomposition method” is another method for oxidizing and decomposing nitrogen compounds in sample water to nitrate ions. This method irradiates the sample water to which alkaline potassium peroxodisulfate, which is an oxidizing agent, is irradiated with ultraviolet rays at a predetermined temperature and pressure, thereby oxidizing and decomposing nitrogen compounds in the sample water to nitrate ions. The total nitrogen concentration is quantified by measuring the absorbance of the sample water at 220 nm. In this method, improvement of lowering the temperature and pressure of the sample water has been promoted, and the temperature required for the oxidative decomposition of nitrogen oxides by ultraviolet rays is lowered from the conventional 120 ° C. to about 60 ° C., and the pressure is also increased. Since the pressure is good at normal pressure, the device is not required to have high pressure resistance and heat resistance.
- the light emitting part of the ultraviolet lamp is inserted into the reaction vessel of the oxidative decomposition part, and the light emitting part is immersed in the sample water.
- the structure in which ultraviolet light is irradiated to a nitrogen compound in sample water in a state see Patent Document 1.
- Patent Document 1 a structure in which ultraviolet light is irradiated to a nitrogen compound in sample water in a state.
- a signal that seems to be affected by a substance different from the nitrate ion produced by the oxidative decomposition of the nitrogen compound was sometimes included in the detection signal. The cause has not been elucidated.
- an object of the present invention is to prevent interference with measurement of total nitrogen by substances other than nitrate ions in the absorbance measurement of sample water containing nitrate ions converted by ultraviolet irradiation.
- the present invention includes a reaction vessel having a space for accommodating a sample in a space around the ultraviolet lamp, in which a light emitting portion of the ultraviolet lamp is inserted, and for oxidizing and decomposing nitrogen compounds in the reaction vessel
- the sample containing the reaction reagent is stored and the sample water is irradiated with UV light from the UV lamp to oxidatively decompose nitrogen compounds and convert them into nitrate ions, and the absorbance of the sample water containing the nitrate ions is measured.
- the total nitrogen measuring device for measuring the total nitrogen concentration of the sample water is characterized in that the holding part for holding the light emitting part of the ultraviolet lamp is made of a material not containing iron.
- the cause of the noise lies in the ultraviolet lamp that irradiates the sample water with ultraviolet rays in order to oxidatively decompose the nitrogen compound. That is, in the ultraviolet lamp, only the light emitting portion made of a material not containing iron-based material such as a quartz glass tube comes into contact with the sample water, but the outer cylindrical portion of the holding portion that holds the base end of the light emitting portion is made of iron. It was composed of system materials. Although the holder does not come into direct contact with the sample water, sample water to which sulfuric acid or the like has been added evaporates and adheres to the surface of the holder, and iron ions may elute from that part and enter the sample water. I found out.
- the holding part for holding the light emitting part of the ultraviolet lamp is made of a material not containing iron. Therefore, even if the reagent that reacts with iron evaporates and adheres to the surface of the holding portion of the ultraviolet lamp, iron ions are not generated, and interference with the total nitrogen measurement by iron ions can be prevented.
- a UV lamp for the oxidation reaction part measure the total nitrogen of the same sample when the outer cylinder part of the holding part is made of iron and when the outer cylinder part of the holding part is made of silicon resin. It is the measurement data when it is performed.
- the holding part that holds the light emitting part of the ultraviolet lamp is made of a resin that does not contain a nitrogen component.
- This total nitrogen measuring device includes two multi-port valves 10a and 10b.
- a sample adjustment tank 1 for adjusting and storing a sample is connected to one port of one multi-port valve 10b via a tube 29.
- the other port of the multi-port valve 10b is connected to the container 8 containing the span solution and the container 9 containing the pure water, the sample inlet / outlet 25 of the oxidation reaction unit 23, the measurement unit 16, and the like.
- the common port of the multi-port valve 10b is connected to one port of the other multi-port valve 10a.
- Containers 2 to 7 containing various solutions are connected to each port of the multi-port valve 10a through pipes.
- the container 2 has a potassium peroxodisulfate solution
- the container 3 has an aqueous sodium hydroxide solution
- the container 4 has a hydrochloric acid solution
- the container 5 has an ascorbic acid solution
- the container 6 has a molybdic acid solution
- the container 7 has a Each contain a sulfuric acid solution.
- a syringe pump 17 is connected to the common port of the multi-port valve 10a.
- the syringe pump 17 is driven by a motor 27 to suck and discharge various liquids.
- the oxidation reaction unit 23 oxidizes and decomposes the nitrogen compound in the sample to nitrate ions.
- a light emitting unit 30 of an ultraviolet lamp 14 such as a low pressure mercury lamp is inserted in the reaction vessel 13, and the sample water 15 is accommodated around the ultraviolet lamp 14.
- the reaction vessel 13 is provided with a heater, and the temperature of the stored sample can be heated to a predetermined temperature.
- the heating temperature of the sample water is preferably 100 ° C. or lower.
- the measurement unit 16 measures the absorbance of the sample water after the oxidation reaction, and detailed illustration is omitted.
- the sensor etc. which detect this are provided.
- the sample water is measured from the sample preparation tank 1 by the syringe pump 17. If necessary, pure water 9 is sucked into the syringe pump 17 and diluted so that the sample water becomes, for example, 2 mgN / L or less.
- a solution obtained by adding the potassium peroxodisulfate solution 2 and the sodium hydroxide solution 3 to the sample water is introduced into the reaction vessel 15 of the oxidation reaction unit 23 heated to about 60 to 80 ° C.
- the ultraviolet lamp 14 irradiates ultraviolet rays for about 20 minutes to oxidatively decompose nitrogen compounds to nitrate ions.
- a fixed amount of the solution after completion of the oxidation reaction is weighed with the syringe pump 17, and the hydrochloric acid solution 4 is added and sent to the measuring unit 16. And the light absorbency in 220 nm is measured in the measurement part 16, and total nitrogen concentration is calculated
- the ultraviolet lamp 14 used in the oxidation reaction section 23 is shown in FIG.
- the ultraviolet lamp 14 includes a light emitting unit 30 at the tip, and a base end portion of the light emitting unit 30 is held by a holding unit 32.
- the holding part 32 has a hole through which the light emitting part 30 penetrates at the distal end of the outer cylinder part 33, and a layer 36 formed by solidifying the filler filled therein holds the base end of the light emitting part 30.
- the outer cylindrical portion 33 of the holding portion 32 is made of a material other than iron such as ceramic, alumina, quartz glass, Pyrex (registered trademark) glass, fluororubber (for example, Viton (registered trademark)), tetrafluoroethylene, or the like.
- examples of the filler for forming the layer 36 in the head portion 33 include a low thermal expansion coefficient silicon resin, epoxy resin, and cement.
- the filler layer 36 is formed of silicon resin, and the epoxy resin layer 40, the silicon resin layer 42, the epoxy resin layer 44, and the silicon resin layer 46 are formed on the opposite side of the silicon resin layer 36 from the light emitting portion 30. Are formed in order from the silicon resin layer 36 side. Two lead wires 34 coming out from the base end of the light emitting unit 30 are drawn out of the holding unit 32 through a caulking clamp 38.
- the oxidation reaction unit 23 only the light emitting unit 30 of the ultraviolet lamp 14 is inserted into the reaction vessel 13, and sample water is accommodated around the light emitting unit 30.
- the sample water to be stored contains potassium peroxodisulfate and sodium hydroxide, and these liquids may evaporate and adhere to the outer cylinder portion of the holding portion 32 of the ultraviolet lamp 14. Since the outer cylinder portion is made of a material other than iron, iron ions that absorb light of 220 nm are not generated, and the measurement of ultraviolet absorbance is not affected.
- FIG. 4 shows the total nitrogen of the same sample in the case where the outer tube portion of the holding portion made of iron is used as the ultraviolet lamp of the oxidation reaction portion and the case where the outer tube portion of the holding portion is made of silicon resin. It is the measurement data when performing the measurement. As shown in this data, when the outer tube portion of the holding portion of the ultraviolet lamp is made of iron, the measured nitrogen concentration increases with time. On the other hand, when the outer cylinder part of the holding part of the ultraviolet lamp is made of silicon resin, the measured nitrogen concentration does not change even if time passes. This is considered that iron is dissolved into the reaction solution in the oxidation reaction section under sulfuric acid acid, and the iron dissolved into the reaction solution affects the measured value of the nitrogen concentration.
- sulfuric acid is added to sample water containing a phosphorus compound, introduced into the oxidative decomposition unit 23, and irradiated with ultraviolet rays at 100 ° C. or lower to convert the phosphorus compound into phosphate ions.
- the phosphorus concentration can also be measured by the molybdenum blue method.
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Abstract
Description
2~9 試薬容器
10a,10b 多ポートバルブ
13 反応容器
14 紫外線ランプ
15 試料水
16 測定部
23 酸化反応部
30 発光部
32 保持部
34 リード線
36 充填剤
この全窒素測定装置は2つの多ポートバルブ10a,10bを備えている。試料を調整して貯留しておくための試料調整槽1はチューブ29を介して一方の多ポートバルブ10bの1つのポートに接続されている。多ポートバルブ10bの他のポートには、スパン液を収容した容器8や純水を収容した容器9のほか、酸化反応部23の試料出入口25、測定部16などが接続されている。また、多ポートバルブ10bの共通ポートは他方の多ポートバルブ10aの1つのポートに接続されている。
酸化反応部23は試料中の窒素化合物を硝酸イオンにまで酸化分解する。酸化反応部23は反応容器13内に低圧水銀ランプなどの紫外線ランプ14の発光部30が挿入されており、その紫外線ランプ14の周囲に試料水15を収容するようになっている。図示は省略されているが、反応容器13にはヒータが設けられており、収容した試料の温度を所定温度に加熱することができる。試料水の加熱温度は100℃以下であることが好ましい。
シリンジポンプ17により試料調整槽1から試料水を計量する。必要に応じて純水9をシリンジポンプ17に吸入し、試料水が例えば2mgN/L以下になるように希釈する。
紫外線ランプ14は、先端に発光部30を備えており、その発光部30の基端部が保持部32に保持されている。保持部32は外筒部33の先端に発光部30を貫通させる孔を備え、その内部に充填された充填剤が固形化されて形成された層36が発光部30の基端を保持している。保持部32の外筒部33は例えばセラミック、アルミナ、石英ガラス、パイレックス(登録商標)ガラス、フッ素ゴム(例えばバイトン(登録商標))、テトラフルオロエチレンなど鉄以外の材料で構成されている。これらの材料を外筒部33に用いた場合、該頭部33内の層36を形成するための充填剤として低熱膨張率のシリコン樹脂、エポキシ樹脂、セメントなどが挙げられる。この実施例では、充填剤の層36がシリコン樹脂で形成され、そのシリコン樹脂層36の発光部30とは反対側にエポキシ樹脂層40、シリコン樹脂層42、エポキシ樹脂層44及びシリコン樹脂層46がシリコン樹脂層36側から順に形成されている。発光部30の基端から出た2本のリード線34はカシメクランプ38を介して保持部32の外部に引き出されている。
Claims (2)
- 内部に紫外線ランプの発光部が挿入され、前記紫外線ランプの周囲の空間に試料を収容するための空間を有する反応容器を備え、その反応容器内に窒素化合物の酸化分解を行なうための反応試薬が添加された試料水を収容して前記紫外線ランプからの紫外線を試料水に照射することにより窒素化合物を酸化分解して硝酸イオンに変換し、その硝酸イオンを含む試料水の吸光度測定を行なうことにより、試料の全窒素濃度を測定する全窒素測定装置において、
前記紫外線ランプの発光部を保持する保持部は鉄を含まない材料により構成されていることを特徴とする全窒素測定装置。 - 前記保持部は窒素成分を含まない樹脂により構成されている請求項1に記載の全窒素測定装置。
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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PCT/JP2012/053790 WO2013121577A1 (ja) | 2012-02-17 | 2012-02-17 | 全窒素測定装置 |
US14/378,694 US9588050B2 (en) | 2012-02-17 | 2012-02-17 | Total nitrogen measurement apparatus |
JP2014500016A JP5854122B2 (ja) | 2012-02-17 | 2012-02-17 | 全窒素測定装置 |
CN201280069341.3A CN104115009B (zh) | 2012-02-17 | 2012-02-17 | 总氮测定装置 |
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PCT/JP2012/053790 WO2013121577A1 (ja) | 2012-02-17 | 2012-02-17 | 全窒素測定装置 |
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JP (1) | JP5854122B2 (ja) |
CN (1) | CN104115009B (ja) |
WO (1) | WO2013121577A1 (ja) |
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JP2015191884A (ja) * | 2014-03-31 | 2015-11-02 | 株式会社島津製作所 | 紫外線照射装置及びこれを備えた分析装置 |
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CN104115009B (zh) | 2016-08-24 |
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