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Food safety national standard -- Method for the determination of thiaden residues in food
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GB 23200.41-2016
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Basic data | Standard ID | GB 23200.41-2016 (GB23200.41-2016) | | Description (Translated English) | Food safety national standard -- Method for the determination of thiaden residues in food | | Sector / Industry | National Standard | | Classification of Chinese Standard | G25 | | Word Count Estimation | 13,124 | | Date of Issue | 2016-12-18 | | Date of Implementation | 2017-06-18 | | Older Standard (superseded by this standard) | SN/T 0655-2012 | | Regulation (derived from) | State Health Commission, Ministry of Agriculture, Food and Drug Administration Notice No. 16 of 2016 | | Issuing agency(ies) | National Health and Family Planning Commission of the People's Republic of China, State Food and Drug Administration |
GB 23200.41-2016: Food safety national standard -- Method for the determination of thiaden residues in food ---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Food safety national standard - Method for the determination of thiaden residues in food
This standard is replaced by previous versions of the standard
situation.
National Standards of People's Republic of China
GB
Replace SN 0655-2012
National standards for food safety
Method for the determination of thiaden residues in food
National food safety standards-
Determination of dimethipin residue in foods
2016-12-18 Release.2017-06-18 Implementation
National Health and Family Planning Commission of the People 's Republic of China
Issued by the Ministry of Agriculture of the People 's Republic of China
State Administration of Food and Drug Administration
Foreword
This standard replaces SN 0655-2012 "Method for the determination of DDT residues in export food".
Compared with SN 0655-2012, the main changes are as follows.
- Standard text format is modified to national standard text format for food safety;
- the name of the "export food" to "food";
- increase the "other food reference implementation" in the standard range.
This standard replaced the previous version of the standard release.
-SN 0655-2012.
National standards for food safety
Method for the determination of thiaden residues in food
1 Scope
This standard specifies rice, cabbage, citrus, potato, tea, chestnut, chicken, fish, pork, beef, liver, honey,
Determination of Naphthol Residues in Eggs and Milk by Gas Chromatography.
This standard applies to rice, cabbage, citrus, potato, tea, chestnut, chicken, fish, pork, beef, liver, honey,
Eggs, milk in the determination of the amount of residues in the twins and confirmed, other food can refer to the implementation.
2 normative reference documents
The following documents are indispensable for the application of this document. For dated references, only the dated edition applies to this
file. For undated references, the latest edition (including all modifications) applies to this document.
GB 2763 National Standard for Food Safety - Maximum Residue Limit of Pesticides in Foodstuffs
GB/T 6682 Analytical laboratory water specifications and test methods
3 principle
The samples were extracted with methanol-water mixed solvent and extracted with n-hexane and trichloromethane. After the liquid-liquid distribution was carried out,
Silica and neutral alumina solid phase extraction column, with a gas chromatograph equipped with an electron capture detector for determination, gas chromatography-mass spectrometer
Confirmation, external standard method.
4 reagents and materials
Unless otherwise specified, all reagents are of analytical grade and water is in accordance with the primary water specified in GB/T 6682.
4.1 Reagents
4.1.1 Methanol (CH4O, 67-56-1). Chromatographic Purification.
4.1.2 n-hexane (C6H14,110-54-3). excellent grade pure.
4.1.3 Trichloromethane (CHCl3, 67-66-3). Chromatographic pure.
4.1.4 Acetone (C3H6O, 67-64-1). Chromatographic pure.
4.1.5 Sodium chloride (NaCl, 7647-14-5).
4.1.6 anhydrous sodium sulfate (Na2SO4,7757-82-6). before use at 650 ℃ for 4 h after burning, stored in a dryer, cooling standby
use.
4.2 solution preparation
4.2.1 Methanol - Aqueous solution (9 1, V/V). Accurately remove 90 mL of methanol and mix with 10 mL of water.
4.2.2 Acetone-Trichloromethane Solution (8 100, V/V). Accurately remove 8 mL of acetone and 100 mL of trichloromethane.
4.2.3 10% sodium chloride solution. accurately weighed 10 g sodium chloride in the beaker by adding the appropriate amount of water dissolved, transferred to 100 mL volumetric flask, set
Capacity to scale, shake.
4.3 standards
4.3.1 Thiaden standard (C6H10O4S2,55290-64-7). purity ≥99%.
4.4 standard solution preparation
4.4.1 Standard stock solution. accurately weighed 50 mg of thiophene pesticide standards (accurate to 0.1 mg) in 50 mL brown volumetric flask, with acetone
Dissolved and constant volume to the scale, shake, the preparation of the concentration of 1000μg/mL standard stock solution, 0 ℃ ~ 4 ℃ dark preservation.
4.4.2 Standard Intermediate Solution. Accurately draw 1.0 mL of the standard stock solution in a 100 mL brown volumetric flask, dissolve with acetone and set the volume
To the scale, the preparation of the concentration of 1 000 μg/mL standard intermediate solution, 0 ℃ ~ 4 ℃ dark preservation.
4.4.3 standard working solution. according to the need to remove a certain volume of the standard intermediate solution diluted to the appropriate concentration of standard working solution
liquid. Standard working solution is ready for use.
4.5 Materials
4.5.1 Florisil Solid Phase Extraction Column. 500 mg, 3 mL, or equivalent.
4.5.2 Neutral Alumina Solid Phase Extraction Column. 500 mg, 3 mL, or equivalent.
5 instruments and equipment
5.1 Gas Chromatograph. Equipped with an electron capture detector (ECD).
5.2 Gas Chromatography-Mass Spectrometer. A negative chemical ionization source (NCI).
5.3 Crusher.
5.4 Tissue crusher.
5.5 Solid phase extraction device.
5.6 Centrifuge. 6 000 r/min.
5.7 Scroll Mixer.
5.8 Rotary Evaporator.
5.9 Analysis of balance. 0.01 g and 0.0001 g.
5.10 chicken heart bottle..200 mL.
6 Preparation and storage of samples
6.1 Preparation of the sample
6.1.1 fruits, vegetables and nuts
Take a representative sample 500 g, can not be washed with water after shredding, with a tissue crusher to sample processed into a slurry. Mix well and put it clean
Of the container, sealed and marked.
6.1.2 Tea and grain
Take a representative sample of 500 g, crushed with a pulverizer and passed through a 40 mesh sieve. Mix well, into a clean sample container, sealed and marked
Mark.
6.1.3 Meat and meat products
Take a representative sample 500 g, cut it, and then use the tissue crusher to process the sample into a slurry, mix it, and mix it into a clean sample
Inside, sealed and marked.
6.1.4 honey and milk
Take a representative sample of 500 g, pour it into a clean enamel mix bucket, stir well and mix it into a clean container.
And mark the mark.
Note. The above sample sampling site according to GB 2763 Appendix A implementation.
6.2 Sample storage
Tea, milk, honey, nuts and cereals and other samples at 0 ℃ ~ 4 ℃ preservation; fruit, vegetables, meat and meat products such as samples in the
-18 ℃ below the frozen storage.
During the operation of the sample preparation, the sample should be protected from contamination or changes in the content of the residue.
7 measurement steps
7.1 Extraction
Weigh 2 g (accurate to 0.01 g) homogeneous sample in a 50 mL stoppered centrifuge tube, add 4 mL of water to mix for 15 min, add 5 mL
Methanol - aqueous solution was placed on a vortex oscillator for 5 min, centrifuged for 4 min (centrifugal velocity 6 000 r/min), and the supernatant was collected
In another 50 mL stoppered centrifuge tube, the residue was repeatedly extracted with 5 mL of methanol-water solution and the extracts were combined. Add 2 to the extract
ML of sodium chloride solution and 5 mL of n-hexane for 2 min, centrifuged for 1 min (centrifugal speed of 5 000 r/min), and discarded and discarded
The alkanes were extracted twice with 5 mL of n-hexane and the n-hexane layer was discarded. Add 5 mL of chloroform for 3 min, centrifuge 1 min (5 000
R/min), absorb the lower layer of chloroform in.200 mL chicken heart bottle, with 5 mL of chloroform and then extracted twice, combined extract, the extraction
The solution was concentrated to about 1 mL in a 40 ° C water bath and purged.
7.2 Purification
A 1 cm high anhydrous sodium sulphate was added to the Florian silica solid phase extraction column and connected to the top of the neutral alumina solid phase extraction column,
The tandem is mounted on a solid phase extraction device. Add 10 mL of acetone-chloroform solution before pre-leaching extraction column, discard the eluent,
When the liquid level to reach the top of the anhydrous sodium sulfate, the sample obtained by the rapid extraction of 7.1 into the solid phase extraction column column, with 2 mL of trichloride
Methane Wash the heart of the chicken and repeat the washing three times. The whole wash solution was transferred to a solid phase extraction column and then washed with 15 mL of acetone-trichloromethane solution
Elution and collection of all effluent in another.200 mL chicken heart flask, sprinkled in a 40 ° C water bath to near dryness, dissolved in acetone to 1.0
ML for GC-ECD determination and GC-MS confirmation.
7.3 Determination
7.3.1 Gas Chromatographic Reference Conditions
A) Column. HP-5 quartz capillary column, (30 m0.32 mm (inner diameter) x 0.25 m), or equivalent.
B) heating process. the initial temperature of 50 ℃, at 20 ℃/min rate rose to 160 ℃, keep 1 min, then 5 ℃/min
The rate rose to 230 ° C for 5 min.
C) Inlet temperature. 250 ° C.
D) Detector temperature. 300 ° C.
E) Carrier gas. nitrogen, purity greater than or equal 99.999%, flow rate 1.0 mL/min.
F) Tail gas. 25 mL/min.
G) Injection method. no split injection, 1.0 min after the opening valve.
H) Injection volume. 1 μL.
7.3.2 Gas Chromatography - Mass Spectrometry Reference Conditions
A) Column. HP-5MS quartz capillary column (30 m x 0.25 mm (inner diameter) x 0.25 μm), or equivalent.
B) column temperature. 100 ℃ for 1 min, at 5 ℃/min rate rose to 160 ℃ for 1 min, then 20 ℃/min
The rate rose to 240 ℃, keep 5 min.
C) Inlet temperature. 250 ° C.
D) chromatographic - mass spectrometer interface temperature. 280 ° C.
E) Carrier gas. helium, purity greater than or equal 99.999%, 1.0 mL/min.
F) Injection volume. 1 μL.
G) Injection method. no split into the sample, 1 min after the valve.
H) ionization mode. negative chemical ion source (NCI).
I) Reactor. methane (40%), flow rate 2.0 mL/min ;.
J) Measurement method. Select the ion monitoring mode (SIM).
K) solvent delay time. 8 min.
7.3.3 Determination and confirmation of chromatography
According to the sample in the thiocyanate due to the content of pesticides, selected concentrations similar to the thiophene standard working solution. Standard working solution and sample solution
The response value of the thiophene pesticide should be within the linear range of the instrument. On the standard working fluid and sample volume of alternating sampling to determine
Retention time qualitative, measured sample solution and standard working fluid peak area compared to quantitative. Under the above gas chromatographic conditions, the thiophene is due to the standard color
The spectrum is shown in Figure A.1.
When the sample is measured, if the retention time of the detected peaks is consistent with the standard sample, the mass spectrometry is confirmed. After deducting the background
In the sample spectrum, the selected ions are present, and the selected ion abundance ratio is consistent with the ion abundance ratio of the standard sample
(Allowable deviation range in Table 1), you can determine the presence of such pesticides or related chemicals in the sample. If you can not confirm, should re-injection,
In the manner of scanning (with sufficient sensitivity) or by adding other confirmed ions or by using other analytical instruments of higher sensitivity.
Under the above gas chromatographic - mass spectrometry conditions, the monitoring ion (m/z) and the ion abundance ratio of the thiophene were 128. 210. 211. 212 = 32. 100. 11. 12,
The total ion chromatogram and negative chemical ion spectrum (NCI) of the thiophene standard are shown in Figure B.1 and Figure C.1.
Table 1 Maximum allowable deviation of relative ion abundance when qualitative confirmation
Relative ion abundance /% > 50 > 20 ~ 50 > 10 ~ 20 ≤10
Relative ion abundance Maximum permissible deviation /% ± 20 ± 25 ± 30 ± 50
7.4 blank test
In addition to the sample, according to the above determination steps.
8 results are calculated and expressed
Use the chromatographic data processor or calculate the residual content of the thiophene pesticide in the sample according to the formula (1). The calculated result is deducted from the blank value.
MA
VCA
(1)
Where.
X - the residual content of the thiophene pesticide in the sample, in milligrams per kilogram (mg/kg);
The peak area of thiophene pesticide in A - sample solution;
SC - Concentration of thiophene pesticide in standard working fluid in micrograms per milliliter (μg/mL);
V - Final volume of volume in milliliters (mL);
SA - peak area of thiophene pesticide in standard working fluid;
M - the mass of the sample represented by the final sample, in grams (g).
Note. The result of the calculation should be subtracted from the blank value, two valid digits should be retained, and three valid digits will be retained when the result is greater than 1 mg/kg.
9 precision
9.1 The ratio of the absolute difference between the two independent determinations obtained under reproducibility and its arithmetic mean (percentage) shall be in accordance with
Appendix E requirements.
9.2 The ratio of the absolute difference between the two independent determinations obtained under reproducibility and its arithmetic mean (percentage) shall be in accordance with
Appendix F requirements.
10% limit and recovery rate
10.1 Quantitation limits
The quantification limit of this method is 0.01 mg/kg.
10.2 Recovery rate
When the levels were 0.01 mg/kg, 0.04 mg/kg, 0.1 mg/kg, the addition rate of the thiophene in the different substrates was increased
See Appendix D.
AA
Appendix A
(Informative)
Sulfate Pesticide Standard Gas Chromatography
A.1 Thiophene Pesticide Standards Gas chromatograms are shown in Figure A.1
Figure A.1 Gas chromatographic chart of the thiophene pesticide standard (0.1 mg/kg)
Min0 5 10 15 20 25
Hz
ECD1 A, front signal (C. \\ CHEM32 \\ 1 \\ DATA \\ DIMETHIPHIN \\ 081209 \\ DIMETHIPHIN.2008-12-09 16-42-45 \\ SIG1000006.D)
.6
.0
.6
4.
frequency/
Time/min
BB
Appendix B
(Informative)
The total ion chromatogram of the thiophene pesticide standard
B.1 The total ion chromatogram of the thiophene pesticide standard is shown in Figure B.1
Figure B.1 Total ion chromatogram of the thiophene pesticide standard (0.1 mg/kg)
Time/min
9 .0 01 0 .0 01 1 .0 01 2 .0 01 3 .0 01 4 .0 01 5 .0 01 6 .0 01 7 .0 01 8 .0 01 9 .0 02 0 .0 02 1. 0 02 2 .0 0
T ime - - >
A bundance
TIC. 0 8 1 2 1 5 0 0 5 .D \\ DATA .MS
Ternary
Abundance
.2
Appendix C
(Informative)
Thiaden Pesticide Standard Quality Spectrum (NCI)
C.1 Thiaden Pesticide Standard Quality Spectrum (NCI) See Figure C.1
Figure C.1 Ternary Pesticide Standard (0.1 mg/kg) Mass Spectrum (NCI)
Abundance
Mass ratio/m/z
Appendix D
(Informative)
The recovery rate of thiophene pesticide in different sample matrix
Table D.1 Recovery rates of thiophene pesticides in different sample matrices
Sample Substrate Add Concentration/(mg/kg) Recovery /% Sample Substrate Add Concentration/(mg/kg) Recovery /%
Rice
0.01 80.2 87.5
Fish
0.01 97.3 109.1
0.04 80.1 94.5 0.04 88.7 107.9
0.10 85.7 94.3 0.10 90.8 106.8
Chinese cabbage
0.01 94.1 106.5
pork
0.01 93.7 101.5
0.04 83.7 106.7 0.04 84.0 96.0
0.10 96.4 104.7 0.10 90.8 106.9
Tangerine
0.01 99.3 105.8
beef
0.01 90.2 101.7
0.04 94.9 104.5 0.04 84.4 101.1
0.10 95.9 104.8 0.10 85.6 99.4
potato
0.01 97.1 109.1
Liver
0.01 93.2 111.3
0.04 88.6 108.9 0.04 83.7 104.5
0.10 96.3 110.6 0.10 87.7 105.2
tea
0.01 73.4 86.5
honey
0.01 92.8 107.8
0.04 77.1 88.1 0.04 91.5 99.9
0.10 77.2 90.2 0.10 95.1 108.1
Chestnut
0.01 81.2 90.2
egg
0.01 91.7 100.1
0.04 81.4 95.4 0.04 95.0 100.7
0.10 83.4 90.7 0.10 85.6 99.4
chicken
0.01 90.2 101.7
milk
0.01 97.8 108.5
0.04 82.3 98.0 0.04 99.6 109.0
0.10 86.297.1 0.10 90.8106.2
Appendix E
(Normative appendix)
Laboratory repeatability requirements
Table E.1 Laboratory repeatability requirements
Measured component content
Mg/kg
Precision
0.001 36
> 0.01
> 1 14
Appendix F
(Normative appendix)
Inter-laboratory reproducibility requirements
Table F.1 Inter-laboratory reproducibility requirements
Measured component content
Mg/kg
Precision
0.001 54
> 0.01
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