阅读说明：本技术 一种测定锡箔中高含量锑的方法 (Method for measuring high-content antimony in tin foil ) 是由 李启华 徐涛 冯莉华 余锦 李利军 于 2019-10-12 设计创作，主要内容包括：一测定锡箔中高含量锑的方法,属化学检测技术领域,包括试剂配制、试料称取、前处理溶解、稀释、波长选择、锑校准溶液配制、电感耦合等离子体原子发射光谱仪检测、分析结果的计算和精密度,实现了锡箔试料前处理溶解快速、锑标准溶液配制匹配性强、抗基体干扰能力强、检测过程容易掌握,检测结果准确可靠。测定范围：w(Sb)1.00％～5.00％。锡箔厚度：0.050mm。本发明解决了锡箔中微量锑的检测方法技术问题,对提高特殊用途锡箔的产品质量、生产效率、降低生产成本,提供了坚实基础；为特殊用途锡箔中高含量锑的快速准确定量分析,提供了可靠依据。(A method for measuring high-content antimony in tin foil belongs to the technical field of chemical detection, and comprises reagent preparation, sample weighing, pretreatment dissolution, dilution, wavelength selection, antimony calibration solution preparation, detection of an inductively coupled plasma atomic emission spectrometer, calculation and precision of an analysis result, so that fast pretreatment dissolution of a tin foil sample, strong matching property of antimony standard solution preparation, strong matrix interference resistance, easy mastering of a detection process and accurate and reliable detection results are realized. Measurement range: w (Sb) 1.00-5.00%. Thickness of tin foil: 0.050 mm. The invention solves the technical problem of the detection method of trace antimony in the tin foil, and provides a solid foundation for improving the product quality and the production efficiency of the tin foil with special purposes and reducing the production cost; provides reliable basis for rapid and accurate quantitative analysis of high-content antimony in tin foil for special purposes.)

1. A method for measuring high-content antimony in tin foil comprises reagent preparation, sample weighing, pretreatment dissolving, diluting, wavelength selection, antimony calibration solution preparation, standard addition, detection of an inductively coupled plasma atomic emission spectrometer, calculation of analysis results and precision; the method is characterized by comprising the following steps:

the method comprises the following steps: reagent preparation

The preparation of the reagent comprises the preparation of water and the preparation of a hydrochloric acid solution and a cosolvent solution; preparation of water: preparing ultrapure water by using an ultrapure water machine, wherein the conductivity requirement of the ultrapure water is not more than 0.10 mS/m; preparing a hydrochloric acid solution: adding ultrapure water into a 400mL beaker, adding hydrochloric acid, and uniformly stirring by using a glass rod; preparation of a cosolvent solution: adding ultrapure water and cosolvent into a 250mL beaker, and uniformly stirring by using a glass rod;

step two: sample weighing

Weighing 0.1000g of a test material from a tin foil test sample by using a ten-thousandth electronic balance, and placing the test material into a 150mL conical flask;

step three: dissolving in a pretreatment

Adding 20mL of hydrochloric acid solution and 10mL of cosolvent solution into a conical flask containing a tin foil test material, and heating at low temperature until the test material is completely dissolved; then, continuing to heat until the solution is bubbled with large bubbles to remove excess hydrogen peroxide; taking down, and cooling to room temperature;

step four: dilution of

Transferring a sample solution which is subjected to pretreatment dissolving treatment and then cooled to room temperature into a 100mL volumetric flask, inserting a glass rod into the volumetric flask during the transfer process, enabling the mouth of the conical flask to be inclined and tightly close to the glass rod, enabling the solution to slowly flow in along the glass rod, and enabling the lower end of the glass rod to be close to the inner wall of the bottleneck but not too close to the mouth of the flask so as to avoid the overflow of the solution; after the sample solution flows to the non-flow state, slightly lifting the conical flask along the glass rod, and enabling a drop of solution attached to the opening of the conical flask to flow back into the conical flask; washing a little solution remained in the conical flask with a little second-level or higher-level water for 3-4 times, and transferring the washing solution to a 100mL volumetric flask according to the method; after the sample solution is completely transferred into the volumetric flask, adding water of second grade or above, diluting to about 3/4 volume, and shaking the volumetric flask for several times (without turning and shaking) for primary mixing; then, continuously adding water of second grade or above, and carefully adding the water by one drop by a dropper when the water is close to the scale mark until the lowest point of the lower meniscus of the sample solution is tangent to the scale mark; tightly covering the glass plug;

pressing the glass stopper with the index finger of the left hand and the tip of the right finger against the bottom edge of the bottle, inverting the volumetric flask and shaking, inverting again to make the bubbles in the solution rise to the top end, repeating the process for 10-15 times, and mixing uniformly;

step five: wavelength selection

Starting an inductively coupled plasma atomic emission spectrometer (ICP-AES), and preheating the instrument equipment for more than 2 h; optimizing the working conditions of the instrument according to the instrument specification, and selecting proper measurement conditions (such as argon pressure, observation height, analysis line, flushing time, integration times and the like);

selecting optimized measurement conditions as recommended working parameters by using a Prodigy XP type inductively coupled plasma atomic emission spectrometer; RF power: 1100W; argon gas input pressure: (85-95) PSI; pump speed: 1.0 mL/min; cooling air flow: 20L/min; auxiliary air flow rate: 0.0L/min; atomizing gas pressure: 30 PSI; plasma torch observation height: 15 mm; sample introduction time: 30 s; integration time: 10 s; argon purity: not less than 99.99%;

after the working conditions of the instrument are optimized, comprehensively considering the content range of antimony element, the linear relation, the recovery rate and the accuracy of the detection result in the element measurement wavelength spectral line, and selecting a proper measurement wavelength; the selected measurement wavelengths were: sb206.833nm and 217.581 nm;

step six: preparation of antimony calibration solution

Dissolving 1.0000g metal antimony (more than or equal to 99.9%) in 20mL aqua regia solution under heating, cooling, transferring into 1000mL volumetric flask, diluting to about 3/4 volume with hydrochloric acid solution (1+1), shaking the volumetric flask several times (without inverted shaking), and mixing; then, continuously adding the hydrochloric acid solution (1+1), and carefully adding the hydrochloric acid solution dropwise by using a dropper when the line is close to the scale mark until the lowest point of the lower meniscus of the antimony solution is tangent to the scale mark; tightly covering the glass plug; pressing the glass stopper with the index finger of the left hand and the tip of the right finger against the bottom edge of the bottle, inverting the volumetric flask and shaking, inverting again to make the bubbles in the solution rise to the top end, repeating the process for 10-15 times, and mixing uniformly; this is a standard solution of antimony (1 mL of this solution contains 1mg of antimony);

preparing a tin standard solution, namely heating and dissolving 5.0000g of metallic tin (more than or equal to 99.9%) in 50mL of hydrochloric acid, cooling, transferring into a 500mL volumetric flask, diluting to about 3/4 volume with a hydrochloric acid solution (1+1), and flatly shaking the volumetric flask for several times (without turning and shaking) for primary mixing; then, continuously adding the hydrochloric acid solution (1+1), and carefully adding the hydrochloric acid solution dropwise by using a dropper when the line is close to the scale mark until the lowest point of the lower meniscus of the antimony solution is tangent to the scale mark; tightly covering the glass plug; pressing the glass stopper with the index finger of the left hand and the tip of the right finger against the bottom edge of the bottle, inverting the volumetric flask and shaking, inverting again to make the bubbles in the solution rise to the top end, repeating the process for 10-15 times, and mixing uniformly; this is a standard solution of tin (1 mL of this solution contains 10mg of tin);

0mL of antimony standard solution, 1.00 mL of antimony standard solution, 2.00 mL of antimony standard solution, 3.00 mL of antimony standard solution, 4.00 mL of antimony standard solution and 5.00mL of antimony standard solution are respectively placed in 6 100mL volumetric flasks, and then 10mL of tin standard solution is added into each volumetric flask; adding water of second grade or above, diluting, and mixing;

step seven: inductively coupled plasma atomic emission spectrometer detection

The detection of the inductively coupled plasma atomic emission spectrometer is realized by clicking a plasma torch to automatically start to ignite, confirming that the operation parameters of the instrument are in a normal range after ignition, ensuring that an atomization system and plasma flame work normally, and stabilizing the instrument for more than 15 min;

measuring the spectral intensity of antimony in the solution to be measured on an inductively coupled plasma atomic emission spectrometer; subtracting the spectrum intensity of the blank solution from each spectrum intensity to obtain a net spectrum intensity; automatically reading the content rho (Sb) of the antimony element in the solution to be detected by an instrument;

step eight: calculation of analysis results

Calculating the analysis result, namely calculating the mass fraction of high-content antimony in the tin foil according to the mass concentration of antimony and beryllium in the sample solution in mg/mL;

the high-content antimony content in the tin foil sample is calculated according to the following formula (1) in terms of mass fraction w (Sb):

in the formula:

ρ (Sb) — the value of the mass concentration of antimony in the test solution in milligrams per milliliter (mg/mL);

v is the value of the volume of the fluid to be tested in milliliters (mL);

m is the value of the mass of the sample in grams (g);

step nine: calculation of precision

Precision, meaning that the difference between the results of the two analyses under reproducible conditions is not greater than the reproducibility values listed in Table 1.

TABLE 1 reproducibility values

Technical Field

The invention belongs to the technical field of alloy element determination, and particularly relates to a method for determining high-content antimony in tin foil by using an inductively coupled plasma atomic emission spectrometer, wherein the determination range is as follows: w (Sb) 1.00-5.00%; thickness of tin foil: 0.050 mm.

Background

Tin is a low-melting-point metal element with bluish white luster, is non-toxic, soft and easy to bend, and has a melting point of 231.89 ℃ and a boiling point of 2260 ℃. There are three allotropes: white tin, gray tin, brittle tin.

Tin is rich in ductility at normal temperature. Particularly, at 100 ℃, the paint has very good spreadability, can be spread into extremely thin tin foil, can be thinned to be less than 0.04mm in thickness, and is mainly used for moisture protection. The metal tin can be made into tin tube and tin foil, and can ensure cleanness, no toxicity and moisture resistance in industry. It has its silhouette in many sectors of the military, instrumentation, electrical and light industries.

Tin not only can be combined with a plurality of metals into various alloys, but also can be combined with a plurality of non-metals to form various compounds, and has wide application in the industries of chemistry, dye, rubber, enamel, glass, plastics, paint, pesticide and the like.

With the development of modern technology, tin foil with high content of antimony for special purposes is also manufactured by using tin, antimony, copper, lead and the like.

In order to meet the production requirements of the novel tinfoil product for special products, the content of high-content antimony in tinfoil must be strictly controlled, which undoubtedly provides the technical requirements for accurate detection for chemical analysis and detection personnel.

The main disadvantages of the current detection method are: the detection process is complex, the pollution of detection elements is serious, and the detection time is long; alternatively, more toxic chemical agents need to be used; or, a large precision ICP-MS instrument is required; alternatively, there is no suitable standard analytical method for tin-based alloys; the requirement of accurately detecting the high-content antimony element in the tin foil cannot be met.

Through the query of the standard information service network in Chongqing city, the inductively coupled plasma atomic emission spectrometry method (measuring range: w (Sb) of high-content antimony element in tin foil is not found at present and is 1.00% -5.00%). In addition, no relevant applicable detection methods have been found in the enterprise standard methods. At present, the development of the inductively coupled plasma atomic emission spectrometry detection method for tin foil with high content of antimony element is still blank.

Disclosure of Invention

The invention aims to solve the problems existing in the prior art and provides a method for measuring high-content antimony in tin foil by using an inductively coupled plasma atomic emission spectrometer. In the method, a sample is dissolved by a hydrochloric acid solution and a cosolvent solution, and then diluted to a certain volume by using water of a second grade or more. On an inductively coupled plasma atomic emission spectrometer, the emission light intensities of antimony elements in an antimony calibration solution and a test solution are respectively measured at the recommended wavelength, the mass concentration of high-content antimony in the test solution is automatically displayed by a detection instrument, and then the mass fraction of antimony in a sample is obtained through conversion.

The invention relates to a method for measuring high-content antimony in tin foil, which comprises the following specific steps:

1. the implementation step one: pretreatment

0.1000g of a sample was weighed by a ten-thousandth electronic balance and placed in a 150mL conical flask. 20mL of hydrochloric acid solution and 10mL of cosolvent solution were added, and the mixture was heated at low temperature until the sample was completely dissolved. Heating is then continued until the solution is bubbled up to remove excess hydrogen peroxide. Taking down, and cooling to room temperature. Transferring into 100mL volumetric flask, during the transferring process, inserting a glass rod into the volumetric flask, inclining the mouth of the conical flask to tightly lean on the glass rod, so that the solution slowly flows along the glass rod, and the lower end of the glass rod is close to the inner wall of the flask neck but not too close to the mouth of the flask, so as to avoid the overflow of the solution. After the sample solution had flowed down, the flask was lifted up slightly along the glass rod while standing upright, and a drop of the solution attached to the mouth of the flask was allowed to flow back into the flask. A small amount of the solution remaining in the Erlenmeyer flask was washed with a small amount of second-order or higher-order water 3 to 4 times, and the washing solution was transferred to a 100mL volumetric flask as described above. After the sample solution was completely transferred to the volumetric flask, water of the second and higher grades was added thereto, and when the volume was diluted to about 3/4 volumes, the volumetric flask was shaken several times (without shaking upside down) to conduct preliminary mixing. And then, continuously adding water of second grade or above, and carefully adding the water by one drop by a dropper when the water is close to the scale mark until the lowest point of the lower meniscus of the sample solution is tangent to the scale mark. The glass stopper is tightly covered.

Pressing the glass stopper with the index finger of the left hand and the tip of the right finger against the bottom edge of the bottle, inverting the volumetric flask and shaking, inverting again to make the bubbles in the solution rise to the top, repeating the above steps for 10-15 times, and mixing uniformly.

2. And the implementation step two: optimization of instrument operating conditions

And starting an inductively coupled plasma atomic emission spectrometer (ICP-AES), and preheating the instrument equipment for more than 2 h. And optimizing the working conditions of the instrument according to the instrument specification, and selecting proper measurement conditions (such as argon pressure, observation height, analysis line, flushing time, integration times and the like).

And (3) selecting optimized measurement conditions as recommended working parameters by using a Prodigy XP inductively coupled plasma atomic emission spectrometer. RF power: 1100W; argon gas input pressure: (85-95) PSI; pump speed: 1.0 mL/min; cooling air flow: 20L/min; auxiliary air flow rate: 0.0L/min; atomizing gas pressure: 30 PSI; plasma torch observation height: 15 mm; sample introduction time: 30 s; integration time: 10 s; argon purity: not less than 99.99 percent.

After the working conditions of the instrument are optimized, comprehensive consideration is carried out in an element measurement wavelength spectral line according to the content range, the linear relation, the recovery rate and the accuracy of the detection result of the antimony element, and a proper measurement wavelength is selected. The selected measurement wavelengths were: sb206.833nm, 217.581 nm.

3. And the implementation step three: preparation of antimony calibration solution

1.0000g of antimony metal (. gtoreq.99.9%) was dissolved in 20mL of aqua regia solution under heating, transferred to a 1000mL volumetric flask after cooling, and shaken several times (without shaking upside down) when diluted to about 3/4 volume with hydrochloric acid solution (1+1) for primary mixing. Then, the hydrochloric acid solution (1+1) is continuously added, and when the scale mark is close, the hydrochloric acid solution is carefully added dropwise by using a dropper until the lowest point of the lower meniscus of the antimony element solution is tangent to the scale mark. The glass stopper is tightly covered. Pressing the glass stopper with the index finger of the left hand and the tip of the right finger against the bottom edge of the bottle, inverting the volumetric flask and shaking, inverting again to make the bubbles in the solution rise to the top, repeating the above steps for 10-15 times, and mixing uniformly. This is a standard solution of antimony (1 mL of this solution contains 1mg of antimony).

A tin standard solution was prepared by dissolving 5.0000g of metallic tin (. gtoreq.99.9%) in 50mL of hydrochloric acid under heating, cooling and transferring into a 500mL volumetric flask, and shaking the flask several times (without shaking upside down) when diluted to about 3/4 volume with hydrochloric acid solution (1+1) for initial mixing. Then, the hydrochloric acid solution (1+1) is continuously added, and when the scale mark is close, the hydrochloric acid solution is carefully added dropwise by using a dropper until the lowest point of the lower meniscus of the antimony element solution is tangent to the scale mark. The glass stopper is tightly covered. Pressing the glass stopper with the index finger of the left hand and the tip of the right finger against the bottom edge of the bottle, inverting the volumetric flask and shaking, inverting again to make the bubbles in the solution rise to the top, repeating the above steps for 10-15 times, and mixing uniformly. This is a standard solution of elemental tin (1 mL of this solution contains 10mg of tin).

0mL of antimony standard solution, 1.00 mL of antimony standard solution, 2.00 mL of antimony standard solution, 3.00 mL of antimony standard solution, 4.00 mL of antimony standard solution and 5.00mL of antimony standard solution are respectively placed in 6 100mL volumetric flasks, and then 10mL of tin standard solution is added into each volumetric flask. Adding water of second grade or above, diluting, and mixing.

5. The implementation step four: inductively coupled plasma atomic emission spectrometer detection

And clicking the plasma torch to automatically start to ignite, confirming that the operation parameters of the instrument are in a normal range after ignition, enabling the atomization system and the plasma flame to work normally, and stabilizing the instrument for more than 15 min.

And measuring the spectral intensity of the antimony element in the solution to be measured on an inductively coupled plasma atomic emission spectrometer. The net spectral intensity was determined by subtracting the spectral intensity of the blank solution from the individual spectral intensities. The instrument automatically reads the content rho (Sb) of the antimony element in the solution to be detected.

6. The implementation step five: calculation of analysis results

And calculating the mass fraction of the high-content antimony in the tin foil according to the mass concentration of antimony and beryllium in the sample solution, wherein the mass concentration is expressed in mg/mL.

The high-content antimony content in the tin foil sample is calculated according to the following formula (1) in terms of mass fraction w (Sb):

in the formula:

ρ (Sb) — the value of the mass concentration of antimony in the test solution in milligrams per milliliter (mg/mL);

v is the value of the volume of the fluid to be tested in milliliters (mL);

m is the value of the mass of the sample in grams (g).

7. The implementation step six: synthetic standard sample verification

(1) Synthetic standards

The amounts of the elements added in the 4 tin foil synthesis standards are shown in Table 1. Wherein the solution contains 0.5% of lead and 0.05% of copper, and is diluted to 100mL with water.

TABLE 1 addition of elements for synthetic standards

Numbering	Adding tin amount/mg	Adding lead in an amount of per mg	Adding copper amount/mg	Antimony quantity/mg
					1#	100	0.50	0.050	1.50
2#	100	0.50	0.050	2.50
					3#	100	0.50	0.050	3.50
4#	100	0.50	0.050	4.50

(2) Measurement and calculation

And clicking the plasma torch to automatically start to ignite, confirming that the operation parameters of the instrument are in a normal range after ignition, enabling the atomization system and the plasma flame to work normally, and stabilizing the instrument for more than 15 min.

And measuring the spectral intensity of the antimony element in the solution to be measured on an inductively coupled plasma atomic emission spectrometer. The net spectral intensity was determined by subtracting the spectral intensity of the blank solution from the individual spectral intensities. The instrument automatically reads the content rho (Sb) of the antimony element in the solution to be detected. The mass fraction of antimony was calculated according to equation (1).

The results of the test on the synthesized standards are shown in Table 2. The detection method is accurate and reliable in measurement result.

TABLE 2 evaluation of test results for synthetic standards

Numbering	Element(s)	Addition amount/mg	Content/%	Assay results%	Absolute difference/%)	Allowable difference/%)	Conclusion
								1#	Sb	1.50	1.50	1.47	0.03	0.08	Meets the requirements
2#	Sb	2.50	2.50	2.55	0.05	0.10	Meets the requirements
								3#	Sb	3.50	3.50	3.46	0.04	0.15	Meets the requirements
4#	Sb	4.50	4.50	4.65	0.15	0.20	Meets the requirements

8. The implementation step seven: recovery test

According to the selected optimized condition, adding antimony element standard solution to make recovery rate test, the recovery rate is (measured total quantity-sample content)/added quantity is multiplied by 100%. Generally, a recovery rate of 95% to 105% is required. The recovery rate of the method for measuring the high-content antimony in the tin foil by using the inductively coupled plasma atomic emission spectrometer is 96.50-102.0%, see table 3. The detection method is accurate and reliable in measurement result.

TABLE 3 recovery test results

Numbering	Assay content/% of	Addition amount/%)	Determination of the sum of	Recovery value/%)	Percent recovery%
						11#	1.25	1.00	2.27	1.02	102.0
12#	2.03	2.00	3.96	1.93	96.50
						13#	2.35	2.50	4.82	2.47	98.80

9. And the implementation step eight: production assessment analysis results

The method for detecting the content of antimony in the tin foil by utilizing the inductively coupled plasma atomic emission spectroscopy is used for detecting the sample of the tin foil to be detected and performing precision tests, and the production examination and analysis results are shown in table 4. The analysis result is accurate and reliable.

TABLE 4 production assessment analysis results

Numbering	Element(s)	Assay results w (Sb)/%	Mean value/%)	Standard deviation/%
					21#	Sb	1.23 1.24 1.26 1.29 1.29 1.29	1.26	0.025
22#	Sb	2.16 2.18 2.18 2.20 2.22 2.24	2.20	0.030
					23#	Sb	3.56 3.59 3.62 3.62 3.66 3.68	3.62	0.044

The method for measuring the high-content antimony in the tin foil by using the inductively coupled plasma atomic emission spectrometer has the following characteristics:

1. establishing a rapid quantitative analysis method for high-content antimony in the tin foil by using an inductively coupled plasma atomic emission spectrometer;

2. measurement range: w (Sb) 1.00-5.00%; thickness of tin foil: 0.050 mm;

3. precision:

reproducibility value

4. The technical problem that the matrix seriously interferes with the detection of the content of the element to be detected in the detection process is solved.

Detailed Description

The present invention will be described in detail below.

1. The implementation step one: pretreatment

0.1000g of a sample was weighed by a ten-thousandth electronic balance and placed in a 150mL conical flask. 20mL of hydrochloric acid solution and 10mL of cosolvent solution were added, and the mixture was heated at low temperature until the sample was completely dissolved. Heating is then continued until the solution is bubbled up to remove excess hydrogen peroxide. Taking down, and cooling to room temperature. Transferring into 100mL volumetric flask, during the transferring process, inserting a glass rod into the volumetric flask, inclining the mouth of the conical flask to tightly lean on the glass rod, so that the solution slowly flows along the glass rod, and the lower end of the glass rod is close to the inner wall of the flask neck but not too close to the mouth of the flask, so as to avoid the overflow of the solution. After the sample solution had flowed down, the flask was lifted up slightly along the glass rod while standing upright, and a drop of the solution attached to the mouth of the flask was allowed to flow back into the flask. A small amount of the solution remaining in the Erlenmeyer flask was washed with a small amount of second-order or higher-order water 3 to 4 times, and the washing solution was transferred to a 100mL volumetric flask as described above. After the sample solution was completely transferred to the volumetric flask, water of the second and higher grades was added thereto, and when the volume was diluted to about 3/4 volumes, the volumetric flask was shaken several times (without shaking upside down) to conduct preliminary mixing. And then, continuously adding water of second grade or above, and carefully adding the water by one drop by a dropper when the water is close to the scale mark until the lowest point of the lower meniscus of the sample solution is tangent to the scale mark. The glass stopper is tightly covered.

Pressing the glass stopper with the index finger of the left hand and the tip of the right finger against the bottom edge of the bottle, inverting the volumetric flask and shaking, inverting again to make the bubbles in the solution rise to the top, repeating the above steps for 10-15 times, and mixing uniformly.

2. And the implementation step two: optimization of instrument operating conditions

And starting an inductively coupled plasma atomic emission spectrometer (ICP-AES), and preheating the instrument equipment for more than 2 h. And optimizing the working conditions of the instrument according to the instrument specification, and selecting proper measurement conditions (such as argon pressure, observation height, analysis line, flushing time, integration times and the like).

And (3) selecting optimized measurement conditions as recommended working parameters by using a Prodigy XP inductively coupled plasma atomic emission spectrometer. RF power: 1100W; argon gas input pressure: (85-95) PSI; pump speed: 1.0 mL/min; cooling air flow: 20L/min; auxiliary air flow rate: 0.0L/min; atomizing gas pressure: 30 PSI; plasma torch observation height: 15 mm; sample introduction time: 30 s; integration time: 10 s; argon purity: not less than 99.99 percent.

After the working conditions of the instrument are optimized, comprehensive consideration is carried out in an element measurement wavelength spectral line according to the content range, the linear relation, the recovery rate and the accuracy of the detection result of the antimony element, and a proper measurement wavelength is selected. The selected measurement wavelengths were: sb206.833nm, 217.581 nm.

3. And the implementation step three: preparation of antimony calibration solution

1.0000g of antimony metal (. gtoreq.99.9%) was dissolved in 20mL of aqua regia solution under heating, transferred to a 1000mL volumetric flask after cooling, and shaken several times (without shaking upside down) when diluted to about 3/4 volume with hydrochloric acid solution (1+1) for primary mixing. Then, the hydrochloric acid solution (1+1) is continuously added, and when the scale mark is close, the hydrochloric acid solution is carefully added dropwise by using a dropper until the lowest point of the lower meniscus of the antimony element solution is tangent to the scale mark. The glass stopper is tightly covered. Pressing the glass stopper with the index finger of the left hand and the tip of the right finger against the bottom edge of the bottle, inverting the volumetric flask and shaking, inverting again to make the bubbles in the solution rise to the top, repeating the above steps for 10-15 times, and mixing uniformly. This is a standard solution of antimony (1 mL of this solution contains 1mg of antimony).

A tin standard solution was prepared by dissolving 5.0000g of metallic tin (. gtoreq.99.9%) in 50mL of hydrochloric acid under heating, cooling and transferring into a 500mL volumetric flask, and shaking the flask several times (without shaking upside down) when diluted to about 3/4 volume with hydrochloric acid solution (1+1) for initial mixing. Then, the hydrochloric acid solution (1+1) is continuously added, and when the scale mark is close, the hydrochloric acid solution is carefully added dropwise by using a dropper until the lowest point of the lower meniscus of the antimony element solution is tangent to the scale mark. The glass stopper is tightly covered. Pressing the glass stopper with the index finger of the left hand and the tip of the right finger against the bottom edge of the bottle, inverting the volumetric flask and shaking, inverting again to make the bubbles in the solution rise to the top, repeating the above steps for 10-15 times, and mixing uniformly. This is a standard solution of elemental tin (1 mL of this solution contains 10mg of tin).

0mL of antimony standard solution, 1.00 mL of antimony standard solution, 2.00 mL of antimony standard solution, 3.00 mL of antimony standard solution, 4.00 mL of antimony standard solution and 5.00mL of antimony standard solution are respectively placed in 6 100mL volumetric flasks, and then 10mL of tin standard solution is added into each volumetric flask. Adding water of second grade or above, diluting, and mixing.

5. The implementation step four: inductively coupled plasma atomic emission spectrometer detection

And clicking the plasma torch to automatically start to ignite, confirming that the operation parameters of the instrument are in a normal range after ignition, enabling the atomization system and the plasma flame to work normally, and stabilizing the instrument for more than 15 min.

And measuring the spectral intensity of the antimony element in the solution to be measured on an inductively coupled plasma atomic emission spectrometer. The net spectral intensity was determined by subtracting the spectral intensity of the blank solution from the individual spectral intensities. The instrument automatically reads the content rho (Sb) of the antimony element in the solution to be detected.

6. The implementation step five: calculation of analysis results

And calculating the mass fraction of the high-content antimony in the tin foil according to the mass concentration of antimony and beryllium in the sample solution, wherein the mass concentration is expressed in mg/mL.

The high-content antimony content in the tin foil sample is calculated according to the following formula (1) in terms of mass fraction w (Sb):

in the formula:

ρ (Sb) — the value of the mass concentration of antimony in the test solution in milligrams per milliliter (mg/mL);

v is the value of the volume of the fluid to be tested in milliliters (mL);

m is the value of the mass of the sample in grams (g).

7. The implementation step six: synthetic standard sample verification

(1) Synthetic standards

The amounts of the elements added in the 4 tin foil synthesis standards are shown in Table 1. Wherein the solution contains 0.5% of lead and 0.05% of copper, and is diluted to 100mL with water.

TABLE 1 addition of elements for synthetic standards

Numbering	Adding tin amount/mg	Adding lead in an amount of per mg	Adding copper amount/mg	Antimony quantity/mg
					1#	100	0.50	0.050	1.50
2#	100	0.50	0.050	2.50
					3#	100	0.50	0.050	3.50
4#	100	0.50	0.050	4.50

(2) Measurement and calculation

And clicking the plasma torch to automatically start to ignite, confirming that the operation parameters of the instrument are in a normal range after ignition, enabling the atomization system and the plasma flame to work normally, and stabilizing the instrument for more than 15 min.

And measuring the spectral intensity of the antimony element in the solution to be measured on an inductively coupled plasma atomic emission spectrometer. The net spectral intensity was determined by subtracting the spectral intensity of the blank solution from the individual spectral intensities. The instrument automatically reads the content rho (Sb) of the antimony element in the solution to be detected. The mass fraction of antimony was calculated according to equation (1).

The results of the test on the synthesized standards are shown in Table 2. The detection method is accurate and reliable in measurement result.

TABLE 2 evaluation of test results for synthetic standards

Numbering	Element(s)	Addition amount/mg	Content/%	Assay results%	Absolute difference/%)	Allowable difference/%)	Conclusion
								1#	Sb	1.50	1.50	1.47	0.03	0.08	Meets the requirements
2#	Sb	2.50	2.50	2.55	0.05	0.10	Meets the requirements
								3#	Sb	3.50	3.50	3.46	0.04	0.15	Meets the requirements
4#	Sb	4.50	4.50	4.65	0.15	0.20	Meets the requirements

8. The implementation step seven: recovery test

According to the selected optimized condition, adding antimony element standard solution to make recovery rate test, the recovery rate is (measured total quantity-sample content)/added quantity is multiplied by 100%. Generally, a recovery rate of 95% to 105% is required. The recovery rate of the method for measuring the high-content antimony in the tin foil by using the inductively coupled plasma atomic emission spectrometer is 96.50-102.0%, see table 3. The detection method is accurate and reliable in measurement result.

TABLE 3 recovery test results

Numbering	Assay content/% of	Addition amount/%)	Determination of the sum of	Recovery value/%)	Percent recovery%
						11#	1.25	1.00	2.27	1.02	102.0
12#	2.03	2.00	3.96	1.93	96.50
						13#	2.35	2.50	4.82	2.47	98.80

9. And the implementation step eight: production assessment analysis results

The method for detecting the content of antimony in the tin foil by utilizing the inductively coupled plasma atomic emission spectroscopy is used for detecting the sample of the tin foil to be detected and performing precision tests, and the production examination and analysis results are shown in table 4. The analysis result is accurate and reliable.

TABLE 4 production assessment analysis results

Numbering	Element(s)	Assay results w (Sb)/%	Mean value/%)	Standard deviation/%
					21#	Sb	1.23 1.24 1.26 1.29 1.29 1.29	1.26	0.025
22#	Sb	2.16 2.18 2.18 2.20 2.22 2.24	2.20	0.030
					23#	Sb	3.56 3.59 3.62 3.62 3.66 3.68	3.62	0.044