CN1945291A - Method for analyzing phosphate in sea water and estuary water - Google Patents
Method for analyzing phosphate in sea water and estuary water Download PDFInfo
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- CN1945291A CN1945291A CN 200610022121 CN200610022121A CN1945291A CN 1945291 A CN1945291 A CN 1945291A CN 200610022121 CN200610022121 CN 200610022121 CN 200610022121 A CN200610022121 A CN 200610022121A CN 1945291 A CN1945291 A CN 1945291A
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- phosphate
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- reaction solution
- tested
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- 229910019142 PO4 Inorganic materials 0.000 title claims abstract description 36
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title claims abstract description 36
- 239000010452 phosphate Substances 0.000 title claims abstract description 36
- 238000000034 method Methods 0.000 title claims abstract description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 239000013535 sea water Substances 0.000 title claims abstract description 12
- 238000004458 analytical method Methods 0.000 claims abstract description 32
- 239000007788 liquid Substances 0.000 claims abstract description 32
- 238000012360 testing method Methods 0.000 claims abstract description 32
- 239000000243 solution Substances 0.000 claims abstract description 23
- 238000005349 anion exchange Methods 0.000 claims abstract description 22
- 238000002347 injection Methods 0.000 claims abstract description 19
- 239000007924 injection Substances 0.000 claims abstract description 19
- 230000003287 optical effect Effects 0.000 claims abstract description 13
- 238000001228 spectrum Methods 0.000 claims abstract 8
- 239000011259 mixed solution Substances 0.000 claims abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
- 239000013078 crystal Substances 0.000 claims description 8
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 claims description 6
- 229940010552 ammonium molybdate Drugs 0.000 claims description 6
- 235000018660 ammonium molybdate Nutrition 0.000 claims description 6
- 239000011609 ammonium molybdate Substances 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 239000012295 chemical reaction liquid Substances 0.000 description 33
- 238000002360 preparation method Methods 0.000 description 9
- 230000000050 nutritive effect Effects 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- AMWVZPDSWLOFKA-UHFFFAOYSA-N phosphanylidynemolybdenum Chemical compound [Mo]#P AMWVZPDSWLOFKA-UHFFFAOYSA-N 0.000 description 4
- 238000001514 detection method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- 239000003957 anion exchange resin Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- IRXRGVFLQOSHOH-UHFFFAOYSA-L dipotassium;oxalate Chemical compound [K+].[K+].[O-]C(=O)C([O-])=O IRXRGVFLQOSHOH-UHFFFAOYSA-L 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- JVICFMRAVNKDOE-UHFFFAOYSA-M ethyl violet Chemical compound [Cl-].C1=CC(N(CC)CC)=CC=C1C(C=1C=CC(=CC=1)N(CC)CC)=C1C=CC(=[N+](CC)CC)C=C1 JVICFMRAVNKDOE-UHFFFAOYSA-M 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
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- 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
一种分析海水、河口水中磷酸盐的方法，测试绘制基线是将标样或被测试样送入阴离子交换柱去除磷酸盐后再经进样阀进入反应分析流路，去除磷酸盐的流体在反应分析流路中先后与第一显色反应液R1和第二显色反应液R2混合，该混合液通过光学流通池产生基线被测绘；测试绘制磷酸盐谱图以通过阴离子交换柱去除磷酸盐后的标样或被测试样为推动液，推动液推动经进样阀进入反应分析流路的标样或被测试样先后与第一显色反应液R1和第二显色反应液R2相混合，在混合过程中，标样或被测试样所含磷酸盐生成有色络合物，含有色络合物的溶液通过光学流通池产生谱图被测绘；将所绘制的试样谱图与标样谱图比较，则可计算出试样中磷酸盐的含量。
A method for analyzing phosphate in seawater and estuary water. The baseline of the test is to send the standard sample or the sample to be tested into the anion exchange column to remove phosphate, and then enter the reaction analysis flow path through the injection valve. In the analysis flow path, it is mixed with the first chromogenic reaction solution R1 and the second chromogenic reaction solution R2 successively, and the mixed solution is drawn through the optical flow cell to generate a baseline; after testing and drawing a phosphate spectrum to remove phosphate through an anion exchange column The standard sample or the sample to be tested is the driving liquid, and the pushing liquid pushes the standard sample or the tested sample that enters the reaction analysis flow path through the injection valve to be mixed with the first color-developing reaction solution R1 and the second color-developing reaction solution R2 successively, During the mixing process, the phosphate contained in the standard sample or the tested sample generates a colored complex, and the solution containing the colored complex passes through the optical flow cell to generate a spectrum and is measured; compare the drawn sample spectrum with the standard spectrum Figure comparison, you can calculate the content of phosphate in the sample.
Description
Technical field
The invention belongs to nutritive salt and analyze field, phosphatic automatic analysis method in particularly a kind of seawater, the river mouth water.
Background technology
ZL02133594.X discloses a kind of nutritive salt autoanalyzer method and has implemented the instrument of this method, phosphate (PO
4 3-) be a kind of in the nutritive salt, the instructions of this patent has been described phosphatic analytical approach in seawater, river mouth water and the industrial sewage in the mode of embodiment: testing and drawing baseline and measured matter spectrogram adopt same liquid flow path; Operating instrument, reference liquid R
GinsengThe mixer and the reactor that are sent in the response analysis stream with standard specimen or sample fully mix, and this mixed liquor produces baseline by optical flow cell and surveyed and drawn; Chromogenic reaction liquid R and reference liquid R
GinsengBe sent to the auto injection valve, standard specimen or sample are sent to the mixer in the response analysis stream, reference liquid R
GinsengThe chromogenic reaction liquid R that promotes " stopper " formula and standard specimen or sample in the response analysis stream mixer and reactor in mix, in the mixed process, tested phosphate generates colored complex, and the solution that contains coloured complex compound enters optical flow cell generation spectrogram and surveyed and drawn; Sample spectrogram and the standard specimen spectrogram drawn are compared, calculate tested phosphatic content in the sample.Chromogenic reaction liquid R is formulated by ammonium molybdate, concentrated hydrochloric acid, ethyl violet, emulsion OP and water, reference liquid R
GinsengOn the basis of chromogenic reaction liquid raw material, increase the screening agent potassium oxalate.Change the interference that test analysis is produced though this kind method has been eliminated salinity, guaranteed measuring accuracy, data processing is easy, preparation chromogenic reaction liquid R and reference liquid R
GinsengRequired reagent is more, reference liquid R in analytic process
GinsengThe amount of expending bigger.
Summary of the invention
The object of the present invention is to provide phosphatic new method in a kind of analysis seawater, the river mouth water, the phosphatic detection of being more convenient for of this kind new method, and can save analytical reagent.
Phosphatic method in analysis seawater of the present invention, the river mouth water, comprise the test analysis of standard specimen and the test analysis of sample, the test analysis of standard specimen and sample includes the testing and drawing of baseline and the testing and drawing of phosphate spectrogram, and testing and drawing baseline and phosphate spectrogram adopt same liquid flow path; The testing and drawing baseline is standard specimen or tested sample to be sent into enter the response analysis stream through sampling valve again after anion-exchange column is removed phosphate, remove phosphatic standard specimen or tested sample and successively mix with the first chromogenic reaction liquid R1 and the second chromogenic reaction liquid R2 in the response analysis stream, this mixed liquor produces baseline by optical flow cell and is surveyed and drawn; Testing and drawing phosphate spectrogram serves as to promote liquid with standard specimen or the tested sample of removing by anion-exchange column behind the phosphate, promoting the liquid promotion successively mixes with the first chromogenic reaction liquid R1 and the second chromogenic reaction liquid R2 mutually through " stopper " formula standard specimen or tested sample that sampling valve enters the response analysis stream, in mixed process, contained phosphate of standard specimen or tested sample and chromogenic reaction liquid react, generate colored complex, the solution that contains coloured complex compound produces spectrogram by optical flow cell and is surveyed and drawn; Sample spectrogram and the standard specimen spectrogram drawn are compared, then can calculate phosphatic content in the sample.
In the said method, the described first chromogenic reaction liquid R1 is ammonium molybdate-sulfuric acid solution, and the concentration of ammonium molybdate is 1.0 * 10
-3Mol/L～2.0 * 10
-3Mol/L, the concentration of sulfuric acid is 0.15mol/L～0.30mol/L, and the described second chromogenic reaction liquid R2 is a crystal violet solution, and the concentration of crystal violet is 2.0 * 10
-5Mol/L～4.0 * 10
-5Mol/L.
The method of the invention has following beneficial effect:
1, owing to serves as to promote liquid with standard specimen or the tested sample removed by anion-exchange column behind the phosphate, thereby the salinity of this promotion liquid and standard specimen and tested sample is consistent automatically, eliminate salinity and changed the interference that test analysis is produced, guaranteed measuring accuracy.
2,, provide a kind of technical scheme of different designs with respect to existing nutritive salt autoanalyzer method.
3, owing to,, saved the reagent of preparation promotion liquid or reference liquid with respect to existing nutritive salt autoanalyzer method to serve as to promote liquid by standard specimen behind the anion-exchange column removal phosphate or tested sample.
4, the reagent of preparation chromogenic reaction liquid reduces, and helps reducing analysis cost.
Description of drawings
Fig. 1 is the flow circuit diagram of phosphatic method in analysis seawater of the present invention, the river mouth water;
Fig. 2 is a kind of chromatogram that phosphate in the seawater is analyzed.
Among the figure, 1-low-lift pump, 2-anion-exchange column, 3-auto injection valve, 4-first mixer, 5-first reactor, 6-second mixer, 7-second reactor, 8-optical flow cell, S-tested sample or standard specimen, the RI-first chromogenic reaction liquid, the R2-second chromogenic reaction liquid.
Embodiment
Embodiment 1
Present embodiment is to the phosphate (PO in the seawater
4 3-) carry out test analysis.
Analytical instrument in the present embodiment uses the disclosed nutritive salt of ZL02133594.X to analyze instrument, but liquid flow path will be changed over structure shown in Figure 1.As shown in Figure 1, liquid flow path is made up of sample introduction stream and response analysis stream.The sample introduction stream is assembled by a four-way low-lift pump 1, anion-exchange column 2, auto injection valve 3 and two chromogenic reaction liquid delivery pipes, two samples or standard specimen delivery pipe; The response analysis stream is connected in sequence by pipe fitting by first mixer 4, first reactor 5, second mixer 6, second reactor 7 and optical flow cell 8, concrete assembling mode is: an end of sample or standard specimen delivery pipe is connected the injection port of another termination auto injection valve 3 with low-lift pump 1; One end of another sample or standard specimen delivery pipe is connected the inlet of another termination anion-exchange column 2 with low-lift pump 1, the outlet of anion-exchange column 2 is connected with the promotion liquid inlet of auto injection valve 3 by pipe fitting; One termination low-lift pump 1 of the first chromogenic reaction liquid R1 delivery pipe, another termination first mixer 4; One termination low-lift pump 1 of the second chromogenic reaction liquid R2 delivery pipe, another termination second mixer 6; The inlet of first mixer 4 is connected by the outlet of pipe fitting with auto injection valve 3.
The light path of optical flow cell 8 is 10mm, and the detection wavelength is 530nm.
Anion-exchange column 2 diameter of section φ 5mm, column length 120mm, column packing are the anion exchange resins of the CEC that has quaternary ammonium functional group of particle diameter 50～80 μ m.Described anion exchange resins can be bought the commercial goods, also can make by oneself, and its preparation method is seen " ion-exchange and polymeric adsorbent " (HeBing Lin, Huang Wenqiang chief editor, Science and Technology of Shanghai education publishing house, February nineteen ninety-five).
Four-way low-lift pump: the flow 0.5ml/min～1.0ml/min of each passage, working pressure 2 * 10
5Pa～3 * 10
5Pa.
The operation steps of test analysis is as follows:
1, required standard specimen and the chromogenic reaction liquid of preparation test analysis
(1) preparation standard specimen
With Na
3PO
4(analyzing pure) preparation standard specimen, each standard specimen PO
4 3-Concentration be respectively: 0,0.200 * 10
-6Mol/L, 0.500 * 10
-6Mol/L, 1.00 * 10
-6Mol/L, 2.00 * 10
-6Mol/L, 4.00 * 10
-6Mol/L.
(2) the preparation first chromogenic reaction liquid R1
Take by weighing ammonium molybdate 2.47g, be dissolved in the 600ml water, add sulfuric acid (1: 1) 34ml, be diluted with water to 1L, promptly being mixed with ammonium molybdate concentration is 2.0 * 10
-3Mol/L, sulfuric acid concentration are the first chromogenic reaction liquid of 0.30mol/L.
(3) the preparation second chromogenic reaction liquid R2
Take by weighing crystal violet 0.02g, be diluted to 1L after separating with 100ml is water-soluble, be mixed with crystal violet concentration 5.0 * 10
-5The stock solution of mol/L is standby, gets stock solution and is diluted with water to crystal violet concentration 3.0 * 10
-5Mol/L is the second used chromogenic reaction liquid of present embodiment.
2, testing and drawing spectrogram
(1) spectrogram of testing and drawing standard specimen
Operating instrument, standard specimen is delivered to anion-exchange column 2 by low-lift pump 1, phosphate in the standard specimen is switched on the anion-exchange column, not phosphatic fluid flows out from anion-exchange column and enters by auto injection valve 3 that first mixer 4 mixes with the first chromogenic reaction liquid R1 that low-lift pump 1 is sent into, this mixed liquor is admitted to second mixer 6 and mixes with the second chromogenic reaction liquid R2 that low-lift pump 1 is sent into after the 5 further mixing of first reactor, this mixed liquor further mixes the laggard optics flow cell 8 of going at second reactor 7, then can obtain a steady baseline on computers.
Tested standard specimen enters stream through the injection port of auto injection valve 3 under the effect of low-lift pump 1, remove standard specimen behind the phosphate as promoting liquid by anion-exchange column 2, promotion liquid inlet through auto injection valve 3 enters stream, the tested standard specimen of promotion liquid promotion " stopper " formula enters first mixer 4 to be mixed with the first chromogenic reaction liquid R1 that low-lift pump 1 is sent into, this mixed liquor further mixes at first reactor 5, in the mixed process, tested phosphate generates phosphorus molybdenum Huang, the solution of phosphorous molybdenum Huang enters second mixer 6 under the promotion that promotes liquid mixes with the second chromogenic reaction liquid R2 that low-lift pump 1 is sent into, this mixed liquor further mixes at second reactor 7, in the mixed process, the yellow colored complex that generates of phosphorus molybdenum, the solution that contains coloured complex compound produces spectrogram by optical flow cell and is surveyed and drawn.
(2) spectrogram of testing and drawing sample
Operating instrument, sample is delivered to anion-exchange column 2 by low-lift pump 1, phosphate in the sample is switched on the anion-exchange column, not phosphatic fluid flows out from anion-exchange column and enters by auto injection valve 3 that first mixer 4 mixes with the first chromogenic reaction liquid R1 that low-lift pump 1 is sent into, this mixed liquor is admitted to second mixer 6 and mixes with the second chromogenic reaction liquid R2 that low-lift pump 1 is sent into after the 5 further mixing of first reactor, this mixed liquor further mixes the laggard optics flow cell 8 of going at second reactor 7, then can obtain a steady baseline on computers.
Tested sample enters stream through the injection port of auto injection valve 3 under the effect of low-lift pump 1, remove sample behind the phosphate as promoting liquid by anion-exchange column 2, promotion liquid inlet through auto injection valve 3 enters stream, promotion liquid promotion " stopper " formula tested sample enters first mixer 4 and mixes with the first chromogenic reaction liquid R1 that low-lift pump 1 is sent into, this mixed liquor further mixes at first reactor 5, in the mixed process, tested phosphate generates phosphorus molybdenum Huang, the solution of phosphorous molybdenum Huang enters second mixer 6 under the promotion that promotes liquid mixes with the second chromogenic reaction liquid R2 that low-lift pump 1 is sent into, this mixed liquor further mixes at second reactor 7, in the mixed process, the yellow colored complex that generates of phosphorus molybdenum, the solution that contains coloured complex compound produces spectrogram by optical flow cell and is surveyed and drawn.The sample spectrogram of being surveyed and drawn is seen Fig. 2.
3, the sample testing result calculates
Sample spectrogram and the standard specimen spectrogram drawn are compared, then can calculate phosphatic content in the sample.
Embodiment 2
Present embodiment is to the phosphate (PO in the river mouth water
4 3-) carry out test analysis.
In the present embodiment, analytical instrument, liquid flow path are identical with embodiment 1, the flow of four-way low-lift pump is identical with embodiment 1 with working pressure, the light path of optical flow cell 8, detection wavelength and anion-exchange column 2 are identical with embodiment 1, standard specimen is identical with embodiment 1, and the test analysis flow process is identical with embodiment 1.Difference from Example 1 is as follows:
1, the first chromogenic reaction liquid R1: ammonium molybdate concentration is 1.0 * 10
-3Mol/L, sulfuric acid concentration are 0.15mol/L.
2, the second chromogenic reaction liquid R2: crystal violet concentration 2.0 * 10
-5Mol/L.
Claims (2)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100221211A CN100478678C (en) | 2006-10-25 | 2006-10-25 | Method for analyzing phosphate in sea water and estuary water |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100221211A CN100478678C (en) | 2006-10-25 | 2006-10-25 | Method for analyzing phosphate in sea water and estuary water |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1945291A true CN1945291A (en) | 2007-04-11 |
| CN100478678C CN100478678C (en) | 2009-04-15 |
Family
ID=38044786
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006100221211A Expired - Fee Related CN100478678C (en) | 2006-10-25 | 2006-10-25 | Method for analyzing phosphate in sea water and estuary water |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100478678C (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101101264B (en) * | 2007-07-26 | 2010-04-14 | 四川大学 | Automatic Analysis Method of Sulfide in Seawater |
| CN101975777A (en) * | 2010-10-28 | 2011-02-16 | 四川大学 | Automatic analysis method of chlorate in water sample |
| CN101509904B (en) * | 2009-03-20 | 2011-11-16 | 四川大学 | Low-voltage ion chromatography for simultaneously analyzing silicates and phosphate in water sample |
| CN102830117A (en) * | 2012-09-18 | 2012-12-19 | 国家海洋局天津海水淡化与综合利用研究所 | Device and method for carrying out continuous flow detection on bicarbonates in water |
| CN104569457A (en) * | 2015-01-13 | 2015-04-29 | 四川大学 | Automatic analysis method for trace divalent nickel in water sample |
| CN104849229A (en) * | 2015-05-20 | 2015-08-19 | 安徽建筑大学 | Method for determining polyphosphate-orthophosphate relation in denitrifying dephosphorization by using mid-infrared spectrum |
| CN111721757A (en) * | 2020-03-06 | 2020-09-29 | 中国农业科学院农业资源与农业区划研究所 | A kind of water body phosphate continuous flow analyzer and detection method |
-
2006
- 2006-10-25 CN CNB2006100221211A patent/CN100478678C/en not_active Expired - Fee Related
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101101264B (en) * | 2007-07-26 | 2010-04-14 | 四川大学 | Automatic Analysis Method of Sulfide in Seawater |
| CN101509904B (en) * | 2009-03-20 | 2011-11-16 | 四川大学 | Low-voltage ion chromatography for simultaneously analyzing silicates and phosphate in water sample |
| CN101975777A (en) * | 2010-10-28 | 2011-02-16 | 四川大学 | Automatic analysis method of chlorate in water sample |
| CN102830117A (en) * | 2012-09-18 | 2012-12-19 | 国家海洋局天津海水淡化与综合利用研究所 | Device and method for carrying out continuous flow detection on bicarbonates in water |
| CN104569457A (en) * | 2015-01-13 | 2015-04-29 | 四川大学 | Automatic analysis method for trace divalent nickel in water sample |
| CN104849229A (en) * | 2015-05-20 | 2015-08-19 | 安徽建筑大学 | Method for determining polyphosphate-orthophosphate relation in denitrifying dephosphorization by using mid-infrared spectrum |
| CN111721757A (en) * | 2020-03-06 | 2020-09-29 | 中国农业科学院农业资源与农业区划研究所 | A kind of water body phosphate continuous flow analyzer and detection method |
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