In fact, it is mainly the detection of ag+
The following cited papers
Determination of chloride ion by molar method
The range of determination of chloride ion by molar method is = 5 ~ 111 mg/L. Zhou Shaoling et al. [2] theoretically pointed out that potassium chromate was used as an indicator, and the titration experiment was carried out with silver nitrate standard solution under neutral or weakly alkaline conditions. Due to the loss of AgCl precipitation and dissolution, 1.44 mg/L chloride ion remained in the solution could not be titrated. Therefore, the determination of water quality with low chloride ion content by molar method will cause greater analysis error and poor determination precision. In the process of titration of chloride ion with AgNO _ 3, Ag+ easily forms Ag (NH _ 3)+with ammonia in the solution, which increases the consumption of AgNO _ 3 and leads to high analytical results. Therefore, the pH value of the solution should be controlled to be neutral when determining the chloride ion content in the water by molar method. Zhou Qiang et al. [3] used the seedlings of barley variety Jian 4 with strong salt tolerance as materials, and determined the chloride ion content in plants by silver nitrate titration. The results show that the linear relationship is good in the range of 1~1.5 mol/L, and the correlation coefficient r is 1.9986, but the standard curve does not pass through the coordinate origin. The recovery rate was 87.73% ~117.78%, and the RSD was 11.81%. The accuracy is only 88.43% and the coefficient of variation < P > is 11.33%.
Molar method is a traditional method of measuring
, but it is more accurate to measure only substances with high chloride content
. Potassium chromate and silver nitrate reagents used in this method are toxic substances, and
discharged into the environment will cause environmental pollution.
The high price of silver nitrate reagent increases the cost of determination
and affects the practicability of the method.
2.2
Spectrophotometry
Spectrophotometry is a method for qualitative and quantitative analysis of the measured
substance by measuring its light absorption at a specific wavelength or within a certain wavelength
.
Yang Xuefen [4]
The content of
chloride ion in industrial phosphorous acid was determined by
spectrophotometry with hydrogen peroxide as oxidant and nitric acid -
glycerol as medium. The system has high stability
, the detection wavelength is 381 nm, the content of chloride ion
is linear in the range of 1~6 g/mL
, the correlation coefficient is 1.9999, and the recovery rate of
is 96%~115%.
Guan Rui et al [5]
By studying the stability
of silver chloride precipitation in gelatin -
ethanol aqueous solution, a
spectrophotometric analysis method for the determination of trace chloride ions was established and applied to the determination of trace chloride ions in process water with
machine.
under the optimum experimental conditions, the chloride ion concentration
showed good linearity in the range of 1~6 mg/L
, the correlation coefficient was 1.9993, the standard
deviation of the method was 1.118, the coefficient of variation was
1.126, and the recovery rate was 1.111% ~ 1.15%. The detection limit of this
method is 1.35× 11
-2
mg/L.
gu ligong [6]
an indirect spectrophotometric method for the determination of
mercury thiocyanate -
ferric nitrate was established by using the reaction of
chloride ions with mercury thiocyanate to generate a slightly
ionized mercury chloride complex under acidic conditions, and releasing an equal
amount of thiocyanate radical to react with iron (III) to generate a
red complex.
This method has high sensitivity and good reproducibility. The method is simple and rapid, and can be used for the determination of trace
chloride ions in water.
chloride * * * precipitation enrichment spectrophotometry
method is a national standard method [7]
. The method uses
lead phosphate precipitation as carrier, and * * precipitates to enrich
trace chloride. After centrifugal separation,
iron nitrate /
perchloric acid solution is used to completely dissolve
precipitate, and mercury thiocyanate /
methanol solution is added for color development. Trace chloride is indirectly determined by spectrophotometer, and the determination range is.
Spectrophotometry can accurately determine micro
amount of chloride ion with high sensitivity and good reproducibility.
The method is simple and
fast. However, the reagents of lead phosphate,
sulfur
mercuric cyanate and methanol used in * * * precipitation enrichment spectrophotometry are toxic substances, which
affect the health of operators, and these reagents are used in a large amount, which will cause serious environmental pollution
if they are discharged directly without treatment.
2.3
turbidimetry
This turbidimetry is developed on the basis of colorimetry, and it is an analysis method based on measuring the intensity of transmitted light
after passing through suspension, and has been used in clinical
analysis,
food analysis,
environmental analysis and
industry.
Chen Zhenhua et al. [8]
studied the determination of Cl
-
by silver nitrate turbidity method under the surface active agent. The results showed that Tween-61
was used as the
stabilizer of AgCl
turbidity at 1.3 mol/L
.
Wang Airong et al. [9]
studied the direct determination of trace chloride ions in acidic copper plating solution with glycol
as solubilizing agent and silver nitrate as precipitating agent by silver chloride turbidimetry without separating copper sulfate
. The wavelength of determination is
441 nm, and the linear range is 1~2 g/mL. It is
Yu Lingyun, et al.: The determination method of chloride ion and its application research industry forum
33
The apparent molar absorption coefficient ε=113 ×
115 in the 31
studied the test conditions of
AgCl
turbidity method for the determination of chloride ion with nonionic microemulsion emulsifier OP/
n-butanol /
n-heptane /
water as medium
. The linear range of this method is
1.2~3.4 mg/L,
r =1.9997,
RSD <:
2.8%, and the recovery rate is 94%~114%. It can be used for the determination of trace
chloride ions in cement raw materials,
raw materials and clinker.
Shen Haiyan [11]
Based on the stability of silver chloride precipitation in
gelatin -
ethanol aqueous solution,
a turbidimetric method for the determination of
trace chloride ions in organic process water was established. The linearity of this method is in the range of 1~6 mg/L,
r =1.9993, and the yield of back
is 95.2%~111.3%. Wang Zhaoxi et al. [12]
set the parameters of the flow injection analyzer
the working wavelength is 451 nm, and the sampling frequency is
61
times /h, and established a
turbidimetric method for the determination of chloride ion content in water with reverse flow injection ratio
. The concentration of chloride ion has a good linear relationship with the absorbance of
in the range of 1.1×
11
-5
~ 11.1× 11
-4
mol/L
, the correlation coefficient
is 1.995, and the recovery rate is 95%
~. 2.49%。
this turbidimetric method is easy to operate, short in analysis time, less in reagents, low in operation cost, simple in detection means, and can be combined with other advanced technologies, such as flow injection, so it is easy to realize automation and programming, and has a very broad prospect. Because
this turbidity method has the above characteristics, it is widely used in analytical science.
2.4
ion chromatography
ion chromatography is a relatively new ion
separation technology. This method has been widely used in environmental monitoring, analysis of salt water, soil,
blood
liquid,
boiler water and
dairy products. Zhang xinshen et al. [13]
used a self-made
ion chromatograph to determine the content of
chloride ions in the waste liquor of pickling,
chrome tanning and
total sewage in leather production. The results show that the concentration of chlorine
ion has a good linear relationship in the range of 11
- 5
~11
- 3
mol/L
, the upper limit of measurement
is 11
- 2
mol/L, and the recovery rate is 98.6. Zhu Ziping [14]
The influence of organic components in emulsion on
determined components and the pollution to chromatographic column were eliminated by extraction
separation method, and the chloride ions in emulsion were detected by ion chromatography. The average recovery rate of standard
is 95%~115%, and the relative standard
standard deviation is better than 4.1%(n=21).
Lu keping
et al [15]
decomposed hydrogen peroxide by heating and refluxing under alkaline conditions, and determined trace chloride ions in it by ion chromatography. The detection limit of
chloride ion in hydrogen peroxide is 1.16 g/mL, and the linear
equation is C=1.155 ×11
- 5
A- 1.
12435.
the linear range is 1.11~15.1
g/mL, and the correlation coefficient between concentration and area is r
=1.9992.
Wang Yanli et al. [16]
used high-purity Cu
powder and
concentrated HNO 3
for redox reaction, and heated at
171
℃ to decompose Cu(NO 3
)2
, and removed most of NO3
-. The recovery rate of Cl
-
is 87.5% ~ 93.7%
RSD (n
= 5) <: 11%。 Yan Liu et al. [17]
used ion color
spectrum double column series method to separate nitric acid samples, and used
ion chromatography conductivity detection method to determine trace chloride ions in nitric acid
filtrate. The concentration
of chloride ion is linear with the peak area of color
spectrum in the range of 1.11~1.31 mg/L
, and the linear correlation coefficient
is r =1.997. The recovery rate of chloride ion is
96.5%~99.1%, and the determination results are relative.
song xiaonian et al [18]
used preconcentration ion
chromatography (sample
was preconcentrated by a concentration column and then came in) to determine trace
amount of chloride ions in high-purity water. After linear regression of the analysis results, the equation was
H = 1.429C- 1.596, where
H
.
C
is chloride ion content, and the linear correlation coefficient is r =
1.9985. The standard curve has a good linear
relationship, which can monitor chloride ions in high-purity deionized water
11
- 9
mg/L
.
ion chromatography is simple and convenient, with high sensitivity
, rapid and accurate measurement, and does not need other chemical reagents. It can be applied to practical analysis quickly,
simply,
efficiently and safely, and
it is especially suitable for continuous measurement
determination of large quantities of reagents.
2.5
atomic absorption method
atomic absorption is a method for quantitative analysis based on the absorption of specific spectral lines by
atomic vapor of the measured substance.
gu yongzuo et al [19]
based on the precipitation reaction of Cl
-
with quantitative Ag
+
to AgCl
, an indirect atomic absorption method for the determination of Cl
-
in water was proposed. The concentration of Cl
-
is linear in the range of 1~51 g/mL
. Qian Chuhong et al. [21]
indirectly determined
trace chloride ion in ammonium adipate by atomic absorption
collection method. By adding ethanol
and atomization synergist, the solubility of AgCl
was reduced and the atomization efficiency was improved, thus
the determination sensitivity was improved. By using
AgNO 3 < The residual Ag
+
was determined to indirectly calculate the content of
chloride ion. The relative standard
deviation was 1.9%~4.8%, and the sensitivity (1%A)
was 1.122 mg/L.
Ye Xiaoping [21]
Using ethanol -
gelatin can
improve the stability of silver chloride precipitation, and
Industry Forum
34
No.15
AEO- 7
surfactant can also significantly improve the atomization efficiency of silver
. The content of silver ions was determined by graphite furnace atomic absorption spectrometry
, and then the content of chlorine ions in rare earth oxide minerals with a fixed valence of
was indirectly determined. The linear range was 21~111
g/L, the correlation coefficient was r = 1.9997,
RSD
=1.27%, and the recovery rate was 92.5.
yang Yan et al. [22]
studied the indirect determination of trace chloride ions in high-purity water of power plant by flame atomic absorption spectrometry. The method uses
AgCl
precipitation to determine the residual Ag
+
indirectly
extracted chloride ion content. The relative standard deviation of the method is 2.3%~8.6%, the recovery rate is
94% ~113%, and the sensitivity (1% A) is
1.129 mg/L. Yuan Zhili et al. [23]
studied that in
acidic environment, chloride ion and silver ion formed
precipitation, and after being dissolved by ammonia water, silver was determined by pyrogen
neutron absorption method, thus indirectly determining the content of
chloride ion. The linear range of chlorine
determined by this method is 1.1~31 g/mL, the correlation
coefficient r = 1.999, the sensitivity is 1.123
g/mL
(1%), and the detection limit is 1.