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Patent application title:

Trace detection method of heavy metals and application thereof

Publication number:

-

Publication date:
Application number:

18/079,405

Filed date:

2022-12-12

βœ… Patent granted

Patent number:

US 11,692,954 B1

Grant date:

2023-07-04

PCT filing:

-

PCT publication:

-

Examiner:

Don K Wong

Agent:

WPAT, PC

Adjusted expiration:

2042-12-12

Abstract:

The invention belongs to the technical field of trace detection, and discloses a heavy metal trace detection method and application thereof. The detection method; comprising the following steps: preparing a quality sample; mixing the quality sample with the sample to be tested according to a specific proportion; using X-ray fluorescence spectrometer to detect trace heavy metals; and using standard curve to realize quantitative analysis of heavy metals. For the purpose of detecting heavy metal elements in tea, the application of this invention can shorten the detection time, avoid the use of a large amount of acid liquor, improve the environmental protection performance, and lower the detection cost, moreover, the obtained standard curve by this invention has high correlation and accurate detection results.

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Classification:

  1. Physics
  2. Measuring ; testing

G01N23/223 »  CPC main

Investigating or analysing materials by the use of wave or particle radiation, e.g. X-rays or neutrons, not covered by groups – , or by measuring secondary emission from the material by irradiating the sample with X-rays or gamma-rays and by measuring X-ray fluorescence

G01N33/14 »  CPC further

Investigating or analysing materials by specific methods not covered by groups -; Food Beverages

G01N2223/076 »  CPC further

Investigating materials by wave or particle radiation secondary emission X-ray fluorescence

G01N2223/60 »  CPC further

Investigating materials by wave or particle radiation Specific applications or type of materials

G01N21/64 IPC

Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light; Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited Fluorescence; Phosphorescence

Description

TECHNICAL FIELD

This invention relates to the technical field of trace detection, particularly related to trace detection method of heavy metals and application thereof.

BACKGROUND

After human consumes foods containing heavy metals, the heavy metals would accumulate in human body, then it would be extremely difficult to degrade and remove the enriched heavy metals out of human body, therefore, even a very small amount of heavy metals can still be harmful to human body due to the enrichment. Heavy metals can interact strongly with protein, enzymes, etc. inside human body, making them lose their activity, or they may accumulate in human organs, causing chronic poisoning.

However, the content of heavy metals in tea is very low, it is difficult to directly detect them by instruments, therefore, the common solution is to apply pretreatment of acid digestion, but, the conventional acid digestion process takes a lot of time, and the accuracy of its testing results is easily affected because of the errors exist in the process of pretreatment of acid digestion.

The prior art uses microwave digestion/wet digestion to pretreat samples, and uses atomic absorption spectrometry/atomic fluorescence spectrometry/inductively coupled plasma mass spectrometry to determine the content of heavy metals in tea samples. However, the following problems still exist in the prior art:

1. a big amount of acid is used during pretreatment, and massive acid mists generated during digestion pollute the environment to a certain extent, and have adverse effects on the health of lab testing personnel;

2. pretreatment of acid digestion is the process of oxidizing organic substances in samples with high-grade nitric acid, perchloric acid, etc. to produce inorganic ions, the process takes longer time, and demands higher economic and time cost.

Therefore, it is urgent to provide a trace detection method of heavy metals and application thereof, which can shorten the detection time of heavy metals in tea, avoid the use massive acid, and reduce the detection cost.

SUMMARY

In view of this, the invention provides trace detection method of heavy metals and application thereof, which improves the detection efficiency of heavy metals in tea, reduces the detection cost and meets the requirements of environmental protection.

Trace detection method of heavy metals, comprising the following steps:

1) preparing a quality sample;

2) mixing the quality sample with the sample to be tested according to a specific proportion;

3) using X-ray fluorescence spectrometer to detect trace heavy metals.

Preferably, the preparation steps of the quality sample in step 1) are as follows: as shown in Table 1, each single standard solution is added to the tea quality sample of GBW 08505, after the addition, the quality sample is freeze-dried, ground at βˆ’4Β° C., evenly mixed and bottled for later use. According to the standard requirements of β€œCNAS-G017-2018 General Principles and Statistical Methods of Standard Reference Materials/Standard Samples”, carrying out the homogeneity test, stability test, uncertainty evaluation, data evaluation, etc. on the quality samples, setting value on the new quality samples for the use laboratory internal control.

TABLE 1
Quality of spiked standard of each element
As Pb Cd Cr Cu Zn Ni
Single standard solution 1000 1000 1000 1000 1000 1000 1000
(mg/L)
Content of quality sample 20 50 10 20 100 100 100
after spiked standard
solution (mg/kg)
Spike mass of single 0.1894 0.4894 0.09968 0.192 0.838 0.613 0.9239
standard solution (mg)

Preferably, the heavy metals include As, Pb, Cd, Cr, Cu, Zn and Ni.

Preferably, in step 2,

when the heavy metal element detected is As, the mass ratio of quality control sample to sample to be detected is 20:0.27;

when the heavy metal element detected is Pb, the mass ratio of the quality control sample to the sample to be detected is 20:0.27;

when the detected heavy metal element is Cd, the mass ratio of the quality control sample to the sample to be detected is 50:1.6;

when the detected heavy metal element is Cr, the mass ratio of the quality control sample to the sample to be detected is 10:0.076;

when the heavy metal element detected is Cu, the mass ratio of the quality control sample to the sample to be detected is 100:24;

when the heavy metal element detected is Zn, the mass ratio of the quality control sample to the sample to be detected is 100:35;

when the heavy metal element detected is Ni, the mass ratio of quality control sample to sample to be detected is 100:5.4.

Preferably, in step 3, the test conditions of X-ray fluorescence spectrometer are described as follows: current range of X-ray tube is 0˜0.2 mA, voltage range is 0˜70 KV, test time range is 0˜10 min, collimator is Ο†5 mm, the optical filter system, containing 4 optical filters, wherein, the optical filter is optimized by heavy metal detection and can be automatically switched, the target excitation, containing a Micro X-ray window.

The other purpose of this invention is to provide the application of trace detection method of heavy metals.

Comparing with the prior art, this invention has the following beneficial effects:

The invention applies the combination of the standard addition method with XRF (X-ray fluorescence spectrometer) to measure the content of heavy metals in tea, which does not need acid digestion, and the test method is simple and efficient; before using XRF for determination, the quality sample is quantitatively added to the sample to be detected, which eliminates the loss and pollution of acid solution, achieves the effect of enriching the elements to be detected, and improves the accuracy of XRF for the detection of heavy metals.

The principle of X-ray fluorescence spectrometer (XRF) for determining the content of elements is: different elements have characteristic X-ray spectra with different wavelengths, and the fluorescence intensity of each spectral line is linearly related to the concentration of elements, therefore, qualitative and quantitative analysis of the elements to be tested can be realized by measuring the wavelength and intensity of the characteristic X-ray lines of elements. Portable XRF can realize in-situ detection of heavy metals, it has advantages of being non-destructive to the sample, and achieving simultaneous determination of multiple elements of the sample, moreover, the detection process takes shorter time, and is easy to operate with lower cost and timely data provision.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 illustrates the standard curve of heavy metals in tea.

DETAILED DESCRIPTION OF EMBODIMENTS

Trace detection method of heavy metals, comprising the following steps:

1) preparing a quality sample;

2) mixing the quality sample with the sample to be tested according to a specific proportion;

3) using X-ray fluorescence spectrometer to detect trace heavy metals.

According to this invention, the preparation steps of the quality sample in step 1) are as follows: as shown in Table 1, each single standard solution is added to the tea quality sample of GBW 08505, after the addition, the quality sample is freeze-dried, and ground at βˆ’4Β° C., evenly mixed and bottled for later use. According to the standard requirements of β€œCNAS-G017-2018 General Principles and Statistical Methods of Standard Reference Materials/Standard Samples”, carrying out the homogeneity test, stability test, uncertainty evaluation, data evaluation, etc. on the quality samples, setting value on the new quality samples for the use laboratory internal control.

TABLE 1
Quality of addition standard of each element
As Pb Cd Cr Cu Zn Ni
Single standard solution 1000 1000 1,000 1000 1000 1000 1000
(mg/L)
Content of quality sample 20 50 10 20 100 100 100
after spiked standard
solution (mg/kg)
Spike mass of single 0.1894 0.4894 0.09968 0.192 0.838 0.613 0.9239
standard solution (mg)

According to this invention, the heavy metals include As, Pb, Cd, Cr, Cu, Zn and Ni.

According to this invention, in step 2,

when the heavy metal element detected is As, the mass ratio of quality control sample to sample to be detected is 20:0.27;

when the heavy metal element detected is Pb, the mass ratio of the quality control sample to the sample to be detected is 20:0.27;

when the detected heavy metal element is Cd, the mass ratio of the quality control sample to the sample to be detected is 50:1.6;

when the detected heavy metal element is Cr, the mass ratio of the quality control sample to the sample to be detected is 10:0.076;

when the heavy metal element detected is Cu, the mass ratio of the quality control sample to the sample to be detected is 100:24;

when the heavy metal element detected is Zn, the mass ratio of the quality control sample to the sample to be detected is 100:35;

when the heavy metal element detected is Ni, the mass ratio of quality control sample to sample to be detected is 100:5.4.

According to this invention, in step 3, the test conditions of X-ray fluorescence spectrometer are described as follows: current range of X-ray tube is 0˜0.2 mA, voltage range is 0˜70 KV, test time range is 0˜10 min, collimator is Ο†5 mm, the optical filter system, containing 4 optical filters, wherein, the optical filter is optimized by heavy metal detection and can be automatically switched, the target excitation, containing a Micro X-ray window.

Drawing of Standard Curve:

The standard curve is based on the standard content of the sample to be tested and the content measured by the instrument, wherein, the two contents shows a linear relationship with the different spike mass. The higher the linear correlation, the more accurate the determination.

As shown in Table 2, adding the quality sample to the sample to be tested, fully mixing, then measuring the content of each element with X-ray fluorescence instrument, setting the determined value as the ordinate, setting the theoretical standard content, which is calculated after adding the spiking solution, as the abscissa, drawing the standard curve, fitting the linear equation, and calculating the spiked recovery (see FIG. 1, Table 3 and Table 4 for details).

TABLE 2
Quality of spiked quality control samples (unit: g)
No. As Pb Cd Cr Cu Zn Ni
 1 0.01 0.01 0.01 0.01 0.01 0.01 0.01
 2 0.02 0.02 0.02 0.02 0.02 0.02 0.02
 3 0.05 0.05 0.05 0.05 0.05 0.05 0.05
 4 0.1 0.1 0.1 0.1 0.1 0.1 0.1
 5 0.2 0.2 0.2 0.2 0.2 0.2 0.2
 6 0.3 0.3 0.3 0.3 0.3 0.3 0.3
 7 0.5 0.5 0.5 0.5 0.5 0.5 0.5
 8 1 1 1 1 1 1 1
 9 1.3 1.3 1.3 1.3 1.3 1.3 1.3
10 1.8 1.8 1.8 1.8 1.8 1.8 1.8
11 3.5 3.5 3.5 3.5 3.5 3.5 3.5
12 5 5 5 5 5 5 5

TABLE 3
Standard curve and correlation coefficient of heavy metals in tea
correlation coefficient
No. Standard curve R2
As y = 0.9817x βˆ’ 0.0697 0.9992
Pb y = 0.9596x + 0.0333 0.9984
Cd y = 1.0133x βˆ’ 0.0214 0.9995
Cr y = 1.0055x βˆ’ 0.0346 0.9943
Cu y = 0.9777x βˆ’ 0.6403 0.9965
Zn y = 1.0666x βˆ’ 4.5605 0.9920
Ni y = 1.0051x βˆ’ 0.8094 0.9924

TABLE 4
Spike recovery value of heavy metals
(As, Pb, Cd, Cr, Cu, Zn, Ni) in tea (unit: %)
No As Pb Cd Cr Cu Zn Ni
 1 104.18 85.82 114.81 92.89 97.30 93.94 96.62
 2 101.69 90.64 106.46 110.44 96.70 93.59 93.48
 3 95.76 91.33 101.00 108.21 94.94 92.58 96.27
 4 93.37 92.55 104.70 102.00 94.15 93.73 96.49
 5 87.28 96.29 94.89 94.33 92.86 93.33 98.47
 6 88.98 94.75 96.00 94.50 91.87 93.07 92.98
 7 91.93 102.00 98.94 92.29 97.06 100.22 85.71
 8 93.58 103.45 95.55 97.07 95.45 93.82 89.76
 9 92.37 93.98 98.88 102.53 100.80 101.21 88.28
10 99.02 96.80 98.41 96.98 95.20 97.69 105.12
11 96.64 97.54 101.70 107.10 95.85 97.14 94.69
12 98.56 94.30 101.69 96.56 96.77 100.74 102.47

This invention also provides the application of of trace detection method of heavy metals.

The technical solutions in the embodiments of the present invention will be clearly and completely described below. Obviously, the described embodiments are only part of the embodiments of the present invention, but not all of them. Based on the embodiment of the present invention, all other embodiments obtained by ordinary technicians in the field without creative labor are within the scope of the present invention.

EMBODIMENT 1

30 tea samples were randomly determined by ICP-MS and X-ray fluorescence instrument, and the relative phase differences between the two independent determination results were calculated, and the results respectively were As 0.34-13.35%, Pb 0.70-11.34%, Cd 0.73-14.97%, Cr 0.61-9.66%, Cu 0.15-7.05%, Zn 0.38-13.20%, Ni 0.28-9.52%, average<20%, meeting the requirements of GB 5009.268 for precision. (The relative phase difference of two independent determination results, when the content>1 mg/kg, the relative phase difference 10%; When the relative phase difference of content≀1 mg/kg and >0.1 mg/kg, the relative phase difference is ≀15%; When the content is ≀0.1 mg/kg, the relative phase difference is ≀20%).

TABLE 5.1
Determination content (mg/kg) and relative phase difference (%) of tea samples
As Pb Cd Cr
No ICPMS XRF RSD % ICPMS XRF RSD % ICPMS XRF RSD % ICPMS XRF RSD %
 1 0.1901 0.2032 βˆ’6.66 0.7687 0.8456 βˆ’9.53 0.0527 0.0554 βˆ’4.95 2.3843 2.3223 2.64
 2 0.0934 0.1009 βˆ’7.70 0.4748 0.5210 βˆ’9.28 0.1779 0.1878 βˆ’5.40 0.7438 0.7220 2.97
 3 0.0877 0.1000 βˆ’13.15 0.5320 0.5543 βˆ’4.10 0.1613 0.1778 βˆ’9.71 0.7346 0.7301 0.61
 4 0.0676 0.0760 βˆ’11.76 0.0675 0.0700 βˆ’3.68 0.0222 0.0253 βˆ’12.99 0.9603 1.0012 βˆ’4.17
 5 0.0962 0.1103 βˆ’13.70 0.0698 0.0770 βˆ’9.86 0.0231 0.0268 βˆ’14.97 1.2691 1.2234 3.67
 6 0.0772 0.0801 βˆ’3.74 0.0888 0.0987 βˆ’10.55 0.0217 0.0245 βˆ’11.97 1.2512 1.2121 3.17
 7 0.0522 0.0560 βˆ’7.05 0.5416 0.5454 βˆ’0.70 0.0344 0.0339 1.52 0.9402 1.0111 βˆ’7.27
 8 0.0700 0.0711 βˆ’1.54 0.0406 0.0450 βˆ’10.19 0.0221 0.0237 βˆ’6.97 0.9149 0.9238 βˆ’0.97
 9 0.0335 0.0355 βˆ’5.82 0.0199 0.0222 βˆ’11.07 0.0488 0.0500 βˆ’2.48 0.7583 0.8019 βˆ’5.58
10 0.0946 0.1023 βˆ’7.78 0.1084 0.1145 βˆ’5.52 0.0286 0.0301 βˆ’5.17 1.2650 1.2323 2.62
11 0.1035 0.1131 βˆ’8.87 0.1613 0.1789 βˆ’10.33 0.0300 0.0321 βˆ’6.74 1.3297 1.2444 6.63
12 0.1172 0.1180 βˆ’0.72 0.1413 0.1567 βˆ’10.34 0.0320 0.0311 2.98 1.0087 1.1111 βˆ’9.66
13 0.1180 0.1298 βˆ’9.50 0.2040 0.1976 3.17 0.0309 0.0311 βˆ’0.73 1.3035 1.2345 5.44
14 0.1087 0.1212 βˆ’10.87 0.2599 0.2500 3.87 0.0322 0.0345 βˆ’6.96 1.3393 1.2988 3.07
15 0.1245 0.1278 βˆ’2.63 0.1267 0.1345 βˆ’6.00 0.0307 0.0298 3.10 1.1802 1.2020 βˆ’1.83
16 0.1583 0.1781 βˆ’11.76 0.1433 0.1345 6.35 0.0297 0.0321 βˆ’7.64 1.1273 1.2023 βˆ’6.44
17 0.0700 0.0789 βˆ’11.88 0.0500 0.0560 βˆ’11.34 0.0176 0.0200 βˆ’12.77 1.1184 1.1987 βˆ’6.93
18 0.1066 0.1100 βˆ’3.15 0.0165 0.0180 βˆ’8.41 0.0348 0.0333 4.35 1.0053 1.0924 βˆ’8.30
19 0.1954 0.2000 βˆ’2.32 0.6696 0.6634 0.93 0.1262 0.1187 6.09 1.3884 1.2901 7.34
20 0.2105 0.2000 5.11 0.1748 0.1699 2.85 0.0972 0.0893 8.43 1.4202 1.2998 8.86
21 0.2774 0.2765 0.34 0.3066 0.2900 5.58 0.0399 0.0387 3.03 1.2716 1.2998 βˆ’2.19
22 0.2618 0.2521 3.79 0.3266 0.3000 8.48 0.0386 0.0376 2.60 1.3766 1.2898 6.51
23 0.0791 0.0800 βˆ’1.11 0.0908 0.1001 βˆ’9.78 0.0412 0.0378 8.62 1.0621 1.1213 βˆ’5.42
24 0.0768 0.0679 12.33 0.1300 0.1200 8.03 0.0392 0.0411 βˆ’4.81 1.0221 1.1010 βˆ’7.43
25 0.0795 0.0876 βˆ’9.64 0.0465 0.0502 βˆ’7.75 0.0248 0.0265 βˆ’6.81 1.4714 1.4747 βˆ’0.22
26 0.1243 0.1421 βˆ’13.35 0.0755 0.0801 βˆ’5.91 0.0279 0.0300 βˆ’7.42 1.3612 1.4721 βˆ’7.83
27 0.1196 0.1234 βˆ’3.10 0.1302 0.1221 6.43 0.0287 0.0300 βˆ’4.58 1.2247 1.3434 βˆ’9.24
28 0.1202 0.1234 βˆ’2.65 0.0820 0.0890 βˆ’8.18 0.0269 0.0289 βˆ’7.00 1.0938 1.1829 βˆ’7.83
29 0.1110 0.1098 1.05 0.1474 0.1348 8.93 0.0251 0.0277 βˆ’9.71 0.9152 1.0000 βˆ’8.85
30 0.1322 0.1298 1.81 0.1321 0.1348 βˆ’2.00 0.0458 0.0444 3.11 1.1379 1.1111 2.38

TABLE 5.2
Determination content (mg/kg) and relative
phase difference (%) of tea samples
NO Cu Zn Ni
 1 ICPMS XRF RSD % ICPMS XRF RSD % ICPMS XRF RSD %
 2 99.85 100.00 βˆ’0.15 0.9444 0.9121 3.48 25.58 23.45 8.70
 3 56.98 57.11 βˆ’0.23 0.1416 0.1421 βˆ’0.38 39.78 38.77 2.57
 4 58.15 62.23 βˆ’6.78 0.2587 0.2433 6.15 41.01 39.01 5.00
 5 61.31 62.33 βˆ’1.65 0.3930 0.4123 βˆ’4.79 17.91 17.23 3.87
 6 64.87 60.11 7.61 0.4438 0.4189 5.77 22.34 20.92 6.55
 7 68.53 70.23 βˆ’2.46 0.5576 0.5328 4.55 23.05 22.22 3.66
 8 54.89 58.90 βˆ’7.05 0.1481 0.1298 13.20 25.41 23.44 8.06
 9 61.49 65.34 βˆ’6.07 0.0776 0.0809 βˆ’4.11 25.31 23.01 9.52
10 71.64 68.99 3.77 0.2593 0.2345 10.06 32.42 30.98 4.53
11 72.15 70.10 2.88 0.6226 0.5789 7.27 21.17 23.01 βˆ’8.34
12 76.77 73.21 4.75 0.6281 0.5982 4.88 22.12 23.89 βˆ’7.67
13 69.83 71.34 βˆ’2.13 0.3347 0.3143 6.28 26.44 24.88 6.08
14 73.32 71.98 1.84 0.9550 1.0010 βˆ’4.70 24.17 24.87 βˆ’2.86
15 71.70 73.45 βˆ’2.42 0.5109 0.5347 βˆ’4.55 25.15 25.55 βˆ’1.59
16 70.35 73.21 βˆ’3.98 0.4467 0.5001 βˆ’11.28 29.33 30.99 βˆ’5.49
17 70.22 73.20 βˆ’4.15 0.8682 0.8989 βˆ’3.47 28.65 30.31 βˆ’5.63
18 59.70 60.54 βˆ’1.40 0.3976 0.3876 2.54 20.94 23.03 βˆ’9.51
19 58.77 61.10 βˆ’3.90 0.7239 0.7014 3.15 25.99 26.79 βˆ’3.02
20 73.01 70.22 3.90 0.7980 0.8123 βˆ’1.78 38.30 40.34 βˆ’5.18
21 73.46 74.32 βˆ’1.17 0.9794 0.9432 3.77 38.77 40.98 βˆ’5.54
22 72.86 75.27 βˆ’3.25 2.1031 1.9879 5.63 26.26 26.33 βˆ’0.28
23 76.01 75.99 0.02 1.9324 1.9989 βˆ’3.38 26.49 25.13 5.27
24 62.77 65.44 βˆ’4.16 0.6838 0.7089 βˆ’3.60 17.16 16.77 2.32
25 63.35 65.01 βˆ’2.58 1.0923 0.9898 9.84 17.15 17.98 βˆ’4.70
26 95.04 98.10 βˆ’3.17 0.8633 0.9001 βˆ’4.17 18.27 19.99 βˆ’8.97
27 85.83 90.13 βˆ’4.88 0.4891 0.4678 4.45 24.86 23.23 6.78
28 81.70 83.33 βˆ’1.97 0.8274 0.8023 3.08 23.94 21.83 9.21
29 70.19 72.43 βˆ’3.14 0.3092 0.3210 βˆ’3.74 17.93 19.15 βˆ’6.56
30 65.30 68.01 βˆ’4.06 0.8801 0.9032 βˆ’2.59 17.48 18.43 βˆ’5.27

In this specification, each embodiment is described in a progressive way, and the differences between each embodiment and other embodiments are highlighted, so the same and similar parts of each embodiment can be referred to each other. The above description of the disclosed embodiments enables those skilled in the art to make or use the invention. Many modifications to these embodiments will be obvious to those skilled in the art, and the general principles defined herein can be implemented in other embodiments without departing from the spirit or scope of the present invention. Therefore, the present invention will not be limited to the embodiments shown herein, but will be accorded the widest scope consistent with the principles and novel features disclosed herein.

Claims

What is claimed is:

1. A trace detection method of heavy metals, comprising steps as follows:

1) Preparing a quality control sample;

2) Mixing the quality control sample with a sample to be tested;

3) Using X-ray fluorescence spectrometer for detection of trace heavy metals;

wherein the heavy metals include As, Pb, Cd, Cr, Cu, Zn and Ni;

wherein in step 2,

when a heavy metal element detected is As, a mass ratio of the quality control sample to the sample to be detected is 20:0.27, a standard curve is y=0.9817xβˆ’0.0697, and a correlation coefficient is 0.9992;

when the heavy metal element detected is Pb, the mass ratio of the quality control sample to the sample to be detected is 20:0.27, a standard curve is y=0.9596x+0.0333, and a correlation coefficient is 0.9984;

when the detected heavy metal element is Cd, the mass ratio of the quality control sample to the sample to be detected is 50:1.6, a standard curve is y=1.0133xβˆ’0.0214, and a correlation coefficient is 0.9995;

when the detected heavy metal element is Cr, the mass ratio of the quality control sample to the sample to be detected is 10:0.076, a standard curve is y=1.0055xβˆ’0.0346, and a correlation coefficient is 0.9943;

when the heavy metal element detected is Cu, the mass ratio of the quality control sample to the sample to be detected is 100:24, a standard curve is y=0.9777xβˆ’0.6403, and a correlation coefficient is 0.9965;

when the heavy metal element detected is Zn, the mass ratio of the quality control sample to the sample to be detected is 100:35, a standard curve is y=1.0666xβˆ’4.5605, and a correlation coefficient is 0.9920;

when the heavy metal element detected is Ni, the mass ratio of quality control sample to sample to be detected is 100:5.4, a standard curve is y=1.0051xβˆ’0.8094, and a correlation coefficient is 0.9924.

2. The trace detection method of heavy metals as claimed in claim 1, wherein in step 3, test conditions of the X-ray fluorescence spectrometer are described as follows: current range of X-ray tube is 0˜0.2 mA, voltage range is 0˜70 KV, test time range is 0˜10 min, collimator is Ο†5 mm, an optical filter system, containing 4 optical filters, wherein, the optical filter is optimized by heavy metal detection and is automatically switched, target excitation, containing a Micro X-ray window.

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Images & Drawings included:

Fig. 01 - Trace detection method of heavy metals and application thereof
Fig. 01
Fig. 02 - Trace detection method of heavy metals and application thereof
Fig. 02

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