CN104865246A - Method for detecting free residual chlorine in drinking water - Google Patents

Method for detecting free residual chlorine in drinking water Download PDF

Info

Publication number
CN104865246A
CN104865246A CN201510260932.4A CN201510260932A CN104865246A CN 104865246 A CN104865246 A CN 104865246A CN 201510260932 A CN201510260932 A CN 201510260932A CN 104865246 A CN104865246 A CN 104865246A
Authority
CN
China
Prior art keywords
water
chlorine
residual chlorine
residual
solution
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
CN201510260932.4A
Other languages
Chinese (zh)
Inventor
赵远
徐波
蔡强
孙向武
陈文艳
肖娴
仇爱峰
俞洁
孙娜
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.)
Changzhou University
Original Assignee
Changzhou University
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 Changzhou University filed Critical Changzhou University
Priority to CN201510260932.4A priority Critical patent/CN104865246A/en
Publication of CN104865246A publication Critical patent/CN104865246A/en
Pending legal-status Critical Current

Links

Landscapes

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

Abstract

The invention discloses a method for detecting free residual chlorine in drinking water and belongs to the field of detection of disinfection by-products of the drinking water. According to the method, an oxidizing agent is added firstly to remove residual organic matters in the water, the content of the free residual chlorine in the water is guaranteed, an o-tolidine dihydrochloride solution is dropwise added to a standard residual chlorine solution to serve as a reagent, and the content of the residual chlorine in the water is calculated finally. The method has the benefits as follows: during detection, chemical reactions of the free residual chlorine with residual compounds in the water can be inhibited, the concentration of the free residual chlorine in the water can be accurately monitored, and the method has the characteristics of good stability, high sensitivity and high accuracy.

Description

Free chlorine residual detection method in a kind of potable water
Technical field
The present invention relates to a kind of detection method of potable water free chlorine, belong to the detection field of disinfection by-product of drinking water.
Background technology
When free chlorine refers to and exists without ammonia chlorine in water, the chlorine added exists with hypochlorous acid and hypochlorite state, this kind of chlorine residue oxidizing force and sterilizing ability strong, but its disinfecting power is not strong, and free chlorine easily contains nitrogen compound generation chemical reaction with ammonium and some produces into combined chlorine, extremely harmful to human body, this project is a very important sanitary index in Drinking Water, contents of residual chlorine in mensuration water and the state of existence, to carrying out drinking water disinfection work and ensureing that water hygiene safety is very important.
At present, having the free chlorine residual in 3 kinds of methods detection potable water, is DPD spectrophotometric method, TMB visual colorimetry and Portable belt chlorine residue instrument method respectively; First being DPD spectrophotometric method, by measuring chlorine residue in the absorbance log of particular range of wavelengths interior focusing, realizing the method for chlorine residue quantitative test, what it detected is limited to 0.01mg/L, there is good degree of accuracy, but all spectrophotometers not Portable belt, be not suitable for Site Detection; Next is TMB visual colorimetry, the method that the absorbance of relevant coloring matter under specific wavelength and residual chlorine concentration meet Lambert-beer's law is generated by chlorine residue and different developer effects, it detects and shows for 0.005mgL, be easy to carry, but the method is easily subject to the factor such as concentration, the nitrite concentration interference of sample acidity, iron; Be finally that Portable belt chlorine residue instrument method detects and is limited to 0.01mg/L, the chlorine residue instrument of use and test paper carrying portable, owing to not being listed in China's national standard detection method, are only used by water factory as self checking method.
Combined chlorine is produced into ammonium and some containing nitrogen compound generation chemical reaction in order to free chlorine residual is easy when solving detection, cause detecting the low problem of free chlorine residual content, the invention discloses free chlorine residual detection method in a kind of potable water, the residual compounds in free chlorine residual and water can be suppressed to carry out chemical reaction, and accurate measurements is to the concentration of the free chlorine residual in water.
Summary of the invention
The present invention can not suppress the residual compounds in free chlorine residual and water to carry out chemical reaction around current chlorine residue detection method, cause detecting the low problem of free chlorine residual content, provide free chlorine residual detection method in a kind of potable water, achieve and content free in water is accurately detected.
In order to achieve the above object, the technical solution adopted in the present invention is:
(1) take out mass concentration juice, be made into mass concentration and be respectively 20 ~ 60g/L concentrated hydrochloric acid, 40 ~ 80g/L o-tolidine solution, stirs, for subsequent use as indicator;
(2) by its mass ratio, the chlorine of 10-30%, the potassium permanganate of 25-40%, the hydrogen peroxide solution Homogeneous phase mixing of 30-65%, places 2-5 minute, preserves at the temperature of 10-25 degree Celsius;
(3) getting sodium hypochlorite is diluted in 25-100ml iodine flask, add 18-90mL potassium iodide, add the pure water of 75-500mL again, shake iodine flask, makes potassium iodide dissolve, and injection iodine flask mixes opens in dark place, leave standstill 2-5 minute, carry out titration with 0.1-0.5mol/L sodium sulphate, with the existing 5-10g/L starch prepared as indicator, calculate its concentration.
Application process of the present invention is: first by adding the method for oxygenant, remove the remaining organism in water, suppress the residual compounds in free chlorine residual and water to carry out chemical reaction, then drip hydrochloric acid o-tolidine solution in standard chlorine residue solution, calculate contents of residual chlorine.
The invention has the beneficial effects as follows: during detection, the residual compounds in free chlorine residual and water can be suppressed to carry out chemical reaction, and accurate measurements, to the concentration of the free chlorine residual in water, has good stability, and sensitivity is high, accuracy is high, characteristic simple to operate.
Embodiment
Preparation method
First take out mass concentration juice, be made into mass concentration and be respectively 20 ~ 60g/L concentrated hydrochloric acid, 40 ~ 80g/L o-tolidine solution, stirs, for subsequent use; Again by its mass ratio, the chlorine of 10-30%, the potassium permanganate of 25-40%, the hydrogen peroxide solution Homogeneous phase mixing of 30-65%, places 2-5 minute, preserves at the temperature of 10-25 degree Celsius; Getting sodium hypochlorite is again diluted in 25-100ml iodine flask, add 18-90mL potassium iodide, add the pure water of 75-500mL again, shake iodine flask, makes potassium iodide dissolve, and injection iodine flask mixes opens in dark place, leave standstill 2-5 minute, carry out titration with 0.1-0.5mol/L sodium sulphate, with the existing 5-10g/L starch prepared as indicator, calculate its concentration.
Application process
First by adding the method for oxygenant, removing the remaining organism in water, suppressing the residual compounds in free chlorine residual and water to carry out chemical reaction, then drip hydrochloric acid o-tolidine solution in standard chlorine residue solution, calculating free state contents of residual chlorine.
Example 1
First take out mass concentration juice, be made into mass concentration and be respectively 20g/L concentrated hydrochloric acid, 40g/L o-tolidine solution, stirs, for subsequent use; Again by its mass ratio, the chlorine of 10%, the potassium permanganate of 25%, the hydrogen peroxide solution Homogeneous phase mixing of 65%, places 2 minutes, preserves at the temperature of 10 degrees Celsius; Getting sodium hypochlorite is again diluted in 25ml iodine flask, add 18mL potassium iodide, add the pure water of 75mL again, shake iodine flask, makes potassium iodide dissolve, and injection iodine flask mixes opens in dark place, leave standstill 2 minutes, carry out titration with 0.1mol/L sodium sulphate, with the existing 5g/L starch prepared as indicator, calculating free state residual chlorine concentration is 0.4mg/L.
Under oxygenant service condition to water in free chlorine residual detect, eliminate disturbing factor, detect the contents of residual chlorine in water.
Example 2
First take out mass concentration juice, be made into mass concentration and be respectively 40g/L concentrated hydrochloric acid, 60g/L o-tolidine solution, stirs, for subsequent use; Again by its mass ratio, the chlorine of 30%, the potassium permanganate of 40%, the hydrogen peroxide solution Homogeneous phase mixing of 3%, places 3 minutes, preserves at the temperature of 15 degrees Celsius; Getting sodium hypochlorite is again diluted in 50ml iodine flask, add 40mL potassium iodide, add the pure water of 200mL again, shake iodine flask, makes potassium iodide dissolve, and injection iodine flask mixes opens in dark place, leave standstill 3 minutes, carry out titration with 0.5mol/L sodium sulphate, with the existing 10g/L starch prepared as indicator, calculating free state contents of residual chlorine is 0.8mg/L.
Under oxygenant service condition to water in free chlorine residual detect, eliminate disturbing factor, detect the contents of residual chlorine in water.
Example 3
First take out mass concentration juice, be made into mass concentration and be respectively 45g/L concentrated hydrochloric acid, 55g/L o-tolidine solution, stirs, for subsequent use; Again by its mass ratio, the chlorine of 25%, the potassium permanganate of 35%, the hydrogen peroxide solution Homogeneous phase mixing of 40%, places 4 minutes, preserves at the temperature of 25 degrees Celsius; Getting sodium hypochlorite is again diluted in 80ml iodine flask, add 85mL potassium iodide, add the pure water of 400mL again, shake iodine flask, makes potassium iodide dissolve, and injection iodine flask mixes opens in dark place, leave standstill 4 minutes, carry out titration with 0.4mol/L sodium sulphate, with the existing 8g/L starch prepared as indicator, calculating free state contents of residual chlorine is 1.2mg/L.
Under oxygenant service condition to water in free chlorine residual detect, eliminate disturbing factor, detect the contents of residual chlorine in water.

Claims (3)

1. a free chlorine residual detection method in potable water, is characterized in that:
(1) by mass concentration, be made into mass concentration and be respectively 20 ~ 60g/L concentrated hydrochloric acid, 40 ~ 80g/L o-tolidine solution, stirs, for subsequent use;
(2) by its mass concentration, be made into the potassium permanganate of 25-40%, the hydrogen peroxide solution Homogeneous phase mixing of 30-65%, place 2-5 minute, preserve at the temperature of 10-25 DEG C.
(3) getting sodium hypochlorite is diluted in 25-100ml iodine flask, add 18-90mL potassium iodide, add the pure water of 75-500mL again, shake iodine flask, makes potassium iodide dissolve, and injection iodine flask mixes opens in dark place, leave standstill 2-5 minute, carry out titration with 0.1-0.5mol/L sodium sulphate, with the existing 5-10g/L starch prepared as indicator, calculate its concentration.
2. free chlorine residual detection method in a kind of potable water according to claim 1, is characterized in that: described oxygenant is potassium permanganate and hydrogen peroxide, by its mass ratio, and the potassium permanganate of 25-80%, the hydrogen peroxide of 30-65%.
3. free chlorine residual detection method in a kind of potable water according to claim 1, is characterized in that: described o-tolidine solution is hydrochloric acid o-tolidine solution.
CN201510260932.4A 2015-05-20 2015-05-20 Method for detecting free residual chlorine in drinking water Pending CN104865246A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510260932.4A CN104865246A (en) 2015-05-20 2015-05-20 Method for detecting free residual chlorine in drinking water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510260932.4A CN104865246A (en) 2015-05-20 2015-05-20 Method for detecting free residual chlorine in drinking water

Publications (1)

Publication Number Publication Date
CN104865246A true CN104865246A (en) 2015-08-26

Family

ID=53911229

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510260932.4A Pending CN104865246A (en) 2015-05-20 2015-05-20 Method for detecting free residual chlorine in drinking water

Country Status (1)

Country Link
CN (1) CN104865246A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106770252A (en) * 2016-12-31 2017-05-31 郑州贯奥仪器仪表有限公司 A kind of Remanent Chloride In Drinking Water detection reagent and its application
CN108982487A (en) * 2018-06-08 2018-12-11 铃木加普腾钢丝(苏州)有限公司 A kind of steel wire hardened line chloride test device and method
CN110286196A (en) * 2019-07-24 2019-09-27 浙江师范大学 A method of with quick, Accurate Determining drinking water chlorine residue on site
CN111638211A (en) * 2020-06-11 2020-09-08 山东信发化工有限公司 Method for detecting chlorate in brine of electrolytic cell
CN113514454A (en) * 2021-06-21 2021-10-19 宜都市友源实业有限公司 Method for detecting free residual chlorine in chlorine-containing organic chemical products
CN115436130A (en) * 2022-09-02 2022-12-06 中国计量科学研究院 Standard substance for simulating free residual chlorine and preparation method thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106770252A (en) * 2016-12-31 2017-05-31 郑州贯奥仪器仪表有限公司 A kind of Remanent Chloride In Drinking Water detection reagent and its application
CN108982487A (en) * 2018-06-08 2018-12-11 铃木加普腾钢丝(苏州)有限公司 A kind of steel wire hardened line chloride test device and method
CN110286196A (en) * 2019-07-24 2019-09-27 浙江师范大学 A method of with quick, Accurate Determining drinking water chlorine residue on site
CN111638211A (en) * 2020-06-11 2020-09-08 山东信发化工有限公司 Method for detecting chlorate in brine of electrolytic cell
CN113514454A (en) * 2021-06-21 2021-10-19 宜都市友源实业有限公司 Method for detecting free residual chlorine in chlorine-containing organic chemical products
CN115436130A (en) * 2022-09-02 2022-12-06 中国计量科学研究院 Standard substance for simulating free residual chlorine and preparation method thereof

Similar Documents

Publication Publication Date Title
CN104865246A (en) Method for detecting free residual chlorine in drinking water
Klassen et al. H2O2 determination by the I3-method and by KMnO4 titration
CN109612951A (en) For detecting chlorine residue in water/total chlorine detection agent and preparation method thereof and detection method
Lee et al. Comparison of colorimetric and membrane introduction mass spectrometry techniques for chloramine analysis
Zhang et al. A novel method for the determination of hydrogen peroxide in bleaching effluents by spectroscopy
CN102564982A (en) Method for determining and correcting cyanide
CN101413894A (en) Iodine content on site rapid quantitative detection reagent in common salt added with iodine and preparation process thereof
CN102778533B (en) Evaluation screening method and evaluation operating process for chlorine-containing disinfectants
CN106841181A (en) A kind of peracetic acid disinfectant quickly determines test paper and preparation method
CN102207466B (en) Rapid test kit for benzoyl peroxide banned additive in flour
CN101532998B (en) A method for detecting chlorine dioxide content in life drinking water
CN101806721B (en) Portable instanteanous tester for concentration of chlorine dioxide solution
JP4944740B2 (en) Chlorite ion measurement method
CN101592612A (en) Test paper for rapidly checking residual content of sterilizing agent
Rahman et al. Quantitative analysis of irbesartan in commercial dosage forms by kinetic spectrophotometry
CN108152288A (en) A kind of method of chlorine dioxide content in detection Drinking Water
CN105527280A (en) Method for detecting chlorine dioxide and chlorite concentration in water through LGB-HRP quantitative injection
Kinani et al. A Critical Review on Chemical Speciation of Chlorine-Produced Oxidants (CPOs) in Seawater. Part 2: Sampling, Sample Preparation and Non-Chromatographic and Mass Spectrometric-Based Methods
JP2010060437A (en) Reagent for measuring peracetic acid concentration and method for measuring peracetic acid concentration
CN105021785A (en) Detection method for combined residual chlorine in drinking water
Linshan et al. Kinetic spectrophotometric determination of vanadium in steels based on the catalytic oxidation of thionine by potassium bromate
Huang et al. Rate of phosphoantimonylmolybdenum blue complex formation in acidic persulfate digested sample matrix for total dissolved phosphorus determination: Importance of post-digestion pH adjustment
Adetoro et al. Electron transfer reaction and mechanism of crystal violet with bromate ion in aqueous hydrochloric acidic medium
CN105510394A (en) Method for detecting content of total organic matters in water in microgravity environment
Edokpayi et al. A kinetic study of the redox reaction of indigo carmine by nitrite ion in aqueous hydrochloric acid medium

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
EXSB Decision made by sipo to initiate substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20150826

WD01 Invention patent application deemed withdrawn after publication