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Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. HJ 866-2017: Water quality. Determination of turpentine. Purge and trap/gas chromatography-mass spectrometry Status: Valid
Basic dataStandard ID: HJ 866-2017 (HJ866-2017)Description (Translated English): Water quality. Determination of turpentine. Purge and trap/gas chromatography-mass spectrometry Sector / Industry: Environmental Protection Industry Standard Classification of Chinese Standard: Z16 Classification of International Standard: 13.060 Word Count Estimation: 11,157 Date of Issue: 2017-11-28 Date of Implementation: 2018-01-01 Quoted Standard: HJ/T 91; HJ/T 164 Regulation (derived from): Ministry of Environmental Protection Announcement 2017 No. 59 Issuing agency(ies): Ministry of Ecology and Environment Summary: This standard specifies the purge and trap/gas chromatographic-mass spectrometry for the determination of turpentine in water. This standard applies to the determination of turpentine in surface water, groundwater, domestic sewage and industrial waste water. When the sample volume is 5 ml, the method detection limit of turpentine is 0.5 ��g/L and the lower limit of determination is 2.0 ��g/L. HJ 866-2017: Water quality. Determination of turpentine. Purge and trap/gas chromatography-mass spectrometry---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. (Water quality turpentine Determination Purge/Trap/GC - MS method) People's Republic of China national environmental protection standards Determination of water quality turpentine Purge trap / Gas chromatography - mass spectrometry Water quality-Determination of turpentine -Purge and trap/gas chromatography-mass spectrometry 2017-11-28 Posted 2018-01-01 implementation Release MEP i directory Foreword ..i 1 Scope 1 2 Normative references 1 3 method principle 1 4 Reagents and materials5 instruments and equipment6 samples .2 7 Analysis Step 2 8 Results Calculation and Presentation 6 9 Precision and accuracy 7 10 Quality Assurance and Quality Control .8 11 Waste treatment .8 i Foreword In order to implement the "Law of the People's Republic of China on Environmental Protection" and the "Law of the People's Republic of China on Prevention and Control of Water Pollution", protect the environment, Ensure human health, regulate the determination of turpentine in water, the development of this standard. This standard specifies the determination of turpentine water purge/gas chromatography - mass spectrometry. This standard is released for the first time. This standard by the Environmental Protection Department of Environmental Monitoring Division and Science and Technology Standards Division to develop. This standard was drafted. China Environmental Monitoring Station. This standard verification unit. Beijing Environmental Protection Monitoring Center, Environmental Monitoring Center of Hebei Province, Zhejiang Province Environmental Monitoring Heart, Chongqing Ecological Environment Monitoring Center, Yangzhou Environmental Monitoring Center Station and Ningbo Environmental Monitoring Center. This standard MEP approved on November 28,.2017. This standard since January 1,.2018 come into operation. This standard is interpreted by the MEP. Determination of quality of turpentine water purge/gas chromatography - mass spectrometry Warning. The reagents and standard solutions used in this method are volatile and toxic compounds. The preparation process should be done in a fume hood Conduct, should be required to wear protective equipment, avoid contact with skin and clothing.1 scope of applicationThis standard specifies the determination of turpentine water purge/gas chromatography - mass spectrometry. This standard applies to the determination of turpentine in surface water, groundwater, domestic sewage and industrial waste water. When the sample volume is 5 ml, the method detection limit of turpentine is 0.5 μg/L and the lower limit of determination is 2.0 μg/L.2 Normative referencesThis standard references the following documents in the terms. For undated references, the effective version applies to this book standard. HJ/T 91 Technical Specifications for Surface Water and Sewerage Monitoring HJ/T 164 Groundwater Environmental Monitoring Technical Specifications3 method principleThe turpentine in water is purged by high-purity helium (or nitrogen) and then adsorbed to the trap. The trap is rapidly heated and purified with high purity After the helium (or nitrogen) is backflushed, the components that have been thermally desorbed are separated by gas chromatography and detected by mass spectrometry. According to pine The main components of oil-saving α-pinene and β-pinene retention time and mass spectrometry and standard material than the qualitative, internal standard method.4 Reagents and materialsUnless otherwise specified, the analysis of the use of analytical reagents in line with national standards, the experimental water is not pure water. 4.1 Methanol (CH3OH). Chromatographic purity. 4.2 Turpentine (C10H16) standard solution. ρ = 500 μg/ml, the solvent is methanol, a certified turpentine mixed standard solution on the market. 4.3 turpentine standard solution. ρ = 20.0 μg/ml. Pipette 400 μl of turpentine standard solution (4.2) into a 10 ml volumetric flask, dilute with methanol (4.1), transfer to poly Tetrafluoroethylene liner Spiral bottle cap brown reagent bottles, stored at 0 ~ 4 C can be stored for one month. 4.4 Internal standard solution. 1,2-dichlorobenzene-d4, ρ =.2000 μg/ml, methanol solvent, a certified standard solution on the market. 4.5 Internal standard solution. ρ = 20.0 μg/ml. 2 Pipet 100 μl of the internal standard solution (4.4) into a 10 ml volumetric flask and dilute to volume with methanol (4.1) and transfer to polytetrafluoroethylene Fluoro ethylene liner screw cap brown reagent bottle, at 0 ~ 4 C can be stored for one month. 4.6 4-Bromofluorobenzene (BFB). ρ = 25 μg/ml, a commercially available certified standard solution. 4.7 Helium, purity ≥99.999%. 4.8 nitrogen, purity ≥99.999%.5 instruments and equipment5.1 Gas Chromatography - Mass Spectrometer. Chromatography section with split/splitless inlet for programmable warming. Part of the mass spectrum with electron impact (EI) Ionization source, with manual/automatic tuning, data acquisition, quantitative analysis and library search and other functions. 5.2 Purge and Trap. with 5 ml purge. Trap tube using 1/3 Tenax, 1/3 silica gel, 1/3 activated carbon mixed adsorbent Or other equivalent adsorbent. 5.3 Column. quartz capillary column, 30 m × 0.25 mm, film thickness 1.4 m, 6% of stationary phase nitrile propyl phenyl/94% dimethyl Polysiloxane, or other equivalent capillary column. 5.4 Vials. 40 ml wide-mouth glass vials with Teflon-lined screw cap. 5.5 Airtight syringe. 5 ml. 5.6 Microprojectors. 10 μl, 25 μl, 50 μl and 250 μl. 5.7 General laboratory equipment and equipment.6 samples6.1 sample collection Collect samples according to HJ/T 91 and HJ/T 164, and slowly introduce the sample into the vial (5.4) along the wall until Full bottles should minimize turpentine escape due to agitation and avoid introducing air bubbles into the sampling bottle. Note. The sample can not add acid. 6.2 Sample preservation Samples collected after 1 ~ 5 C refrigerated transport. Shipped back to the laboratory as soon as possible after analysis, or should be 1 ~ 5 C stored in refrigeration, 2 d Analysis is completed.7 Analysis steps7.1 Instrument reference conditions 7.1.1 Purge and Trap Reference Conditions 3 Sample volume 5.0 ml Purge temperature. 40 ° C Purge flow. 40 ml/min Purge time. 11 min Desorption temperature. 180 ° C; Desorption time. 1 min; Baking temperature. 190 ° C; Baking time. 10 min. Other parameters refer to the use of the instrument Set the Ming book. 7.1.2 GC reference conditions Program temperature. 38 C for 1.0 min, with 5 C/min rose to 150 C, and then 25 C/min rose to 230 C, Paul Hold 3.0 min; Inlet temperature. 230 ° C; Carrier gas flow. 1.0 ml/min; Injection mode. Split injection (split ratio 25. 1). 7.1.3 Reference conditions for mass spectrometry analysis Electron impact source. EI source; Ionization energy. 70 eV; Ion source temperature. 230 ° C; Transmission line temperature. 250 ° C; Scanning Method. Full scan; Scanning range. 35 ~ 300 amu; Solvent delay time. 6.0 min; Other parameters refer to instrument usage Set the Ming book. Note. In order to improve the sensitivity, the method of selective ion scan can also be used for the analysis. For the selection of the quantitative ions and the auxiliary ions, see Table 2. 7.2 Calibration 7.2.1 instrument performance check Gas chromatograph - mass spectrometers must perform instrument performance checks before analyzing samples. Pipette 2 μl of 4-Bromofluorobenzene (4.6) through Inject directly through the gas chromatographic inlet or use a volumetric flask to prepare a 4-Bromofluorobenzene solution at a concentration of 25.0 μg/L, The sample was desorbed and trapped and analyzed by Gas Chromatography-Mass Spectrometer. Analysis conditions refer to 7.1. The resulting 4-Bromofluorobenzene key ions Abundance should meet the requirements in Table 1, otherwise the mass spectrometer parameters need to be adjusted or cleaned ion source. Table 1 4-Bromofluorobenzene key ion abundance criteria Mass ion abundance standard mass ion abundance standard 50% by mass 95% ~ 40% 174 more than 95% by mass 95% 95 Base Peak, 100% Relative Abundance 175 5% to 9% of mass 174 96 95% to 95% of mass 95 176% to 95% to 95% 173 Less than 2% of mass 174 177 5% to 10% of mass 176 7.2.2 Calibration curve drawing Pipette a certain amount of turpentine standard solution (4.3) quickly added to the experimental water with 50 ml volumetric flask, set To volume, preparation of low, high concentration of two series. Low-concentration series were 2.0 μg/L, 4.0 μg/L, 10.0 μg/L, 20.0 μg/L, 40.0 μg/L, take turpentine standard solution (4.3) were 5.0 μl, 10.0 μl, 25.0 μl, 50.0 μl, 100 μl; High concentration series of 40.0 μg/L, 100 μg/L,.200 μg/L, 400 μg/L, 1.00 × 103 μg/L, The solutions (4.3) were 0.10 ml, 0.25 ml, 0.50 ml, 1.00 ml, 2.50 ml, respectively. Use a 5 ml airtight syringe Pipette 5.0 ml of the standard solution and add 5.0 μl of the standard internal standard solution (4.5), according to the reference conditions of 7.1, from the low concentration 4 To high concentration followed by determination, record the standard series of target and internal standard retention time, the quantitative ion response. In practice, depending on the concentration range of turpentine in the sample to be tested, a series of low concentration calibration curves or high Concentration series calibration curve. Under normal circumstances, the surface water, groundwater, domestic sewage test selected 2.0 ~ 40.0 g/L Standard series, industrial wastewater test based on the concentration range may choose to formulate low concentration or high concentration standard series. Note 1. If using a purge trap with an autosampler, the procedure described above can be performed according to the instrument instructions. Note 2. The calibration series solutions are not stable and therefore need to be ready for use. Note 3. The purge and traps should be baked after each start-up and before shutdown to ensure that the system is not contaminated. Under the chromatographic conditions specified in this standard, the total ion chromatogram of the target compound is shown in Figure 1. 1-α-pinene; 2-β-pinene; 3-1,2-dichlorobenzene-d4 (internal standard) Figure 1 Total ion current plot of target compounds 7.2.2.1 Calculation method of average relative response factor The relative response factor (RRFi) of turpentine in the calibration series point i is calculated according to formula (1). IS ISi AA RRF ) (21 (1) Where. RRFi - the relative response factor for the ith turpentine in the calibration series; A1i - Response values of α-pinene quantitation ions at point i in the calibration series; A2i - the response value of the ith pinene-enriched ion in the calibration series; AISi - Calibration value of the i-th internal standard quantitation ion in the calibration series; IS - Concentration of internal standard in the calibration series, μg/L; - Concentration of turpentine at point i in the calibration series, μg/L. 1 6 .0 0 1 7 .0 0 1 8 .0 0 1 9 .0 0 2 0 .0 0 2 1 .0 0 2 2 .0 0 2 3 .0 0 Time - - > Abundance TIC. Turpentine 5 0 ppb - 5 .D \\ data .ms Time (min) 5 Turpentine average relative response factor RRF, calculated according to equation (2). RRF RRF i 1 (2) Where. RRF - turpentine average relative response factor; RRFi - Relative response factor for point i turpentine in the calibration series; n - Calibration series points. The standard deviation of the RRF is calculated according to equation (3). RRFRRF SD (3) Where. SD - standard deviation of RRF; RRF - turpentine average relative response factor; RRFi - Relative response factor for point i turpentine in the calibration series; n - Calibration series points. The relative standard deviation of RRF is calculated according to equation (4). 0 RRF SD RSD (4) Where. RSD - RRF relative standard deviation; SD - standard deviation of RRF; RRF - Turpentine average relative response factor. 7.2.2.2 Calibration curve method Taking the ratio of turpentine concentration to internal standard concentration as abscissa, the sum of the response values of α-pinene and β-pinene quantitative ion and Standard quantitative ion response value of the ratio of the vertical axis, draw the calibration curve. 7.3 Determination After the sample is returned to room temperature, a 5.0 ml sample is aspirated with a gas-tight syringe and 5.0 μl of an internal standard is added to the sample With liquid (4.5), the sample concentration of 20.0 μg/L internal standard, the sample quickly injected into the purge tube, according to the instrument reference conditions (7.1) using the calibration curve of 7.2.2. The autosampler purge trap can refer to the instrument instructions Make. NOTE 1 After analysis of a high concentration sample, one or more blank samples should be analyzed for cross-contamination. 6 Note 2. Determination of industrial wastewater samples, if the turpentine concentration is higher, it is recommended to dilute before measuring. 7.4 Blank test Replace the sample with the experimental water, and perform the blank test according to the same measurement procedure (7.3) as the sample.8 results calculated and said8.1 Qualification of the target compound According to the sample turpentine main components α-pinene and β-pinene retention time, mass spectrometry, fragment ion mass ratio and abundance Degree and other information and qualitative comparison of the standard material. The calibration solution should be repeatedly analyzed to obtain the mean value of the retention time of the target The standard deviation of ± 3 times the retention time is the retention time window, and the retention time of the target in the sample should be within its range. All ions with a relative abundance above 30% of the target's standard spectrum should exist in the sample's spectrum, and the sample's spectrum And the standard spectrum of the above characteristic ions relative abundance deviation should be within ± 30%. 8.2 Quantification of the target compound After the qualitative identification of the target compound, according to the quantitative ion response value, calculated by internal standard method. Quantitative ion of target See Table 2 for auxiliary ions. Table 2 Quantitative ions and auxiliary ions for compounds List No. Target Type Quantum ion-assisted ion 1 α-Pinene Target Compound 93 92,91,77 2 β-Pinene Target Compound 93 41,69,39 3 1,2-Dichlorobenzene-d4 Internal standard 150 152,115 8.2.1 Quantified by the average relative response factor When the target compound is calculated using the average relative response factor, the mass concentration of turpentine in the sample, x, (5) to calculate. RRFA fAA IS ISxx x ) (21 (5) Where. x - sample mass turpentine concentration, μg/L; Response of A1x - α-pinene to quantified ions; A2x - β-pinene quantitative ion response value; AIS - Internal standard quantitative ion response value; IS - mass concentration of internal standard, μg/L; 7RRF - average relative response factor for turpentine; f - dilution factor. 8.2.2 Quantitative calibration curve When the target compound is quantified by the calibration curve method, based on the sum of the quantitative ion response values of α-pinene and β-pinene, The mass concentration of turpentine is obtained directly from the calibration curve. The concentration of turpentine in the sample, x, is calculated according to equation (6). fx 1 (6) Where. x - turpentine mass concentration in the sample, μg/L; 1 - turpentine concentration obtained from the calibration curve, μg/L; f - dilution factor. 8.3 results indicated When the determination results < 100 μg/L, 1 digit after the decimal point is retained; when the measurement result is ≥100 μg/L, 3 digits are valid digital.9 precision and accuracy9.1 Precision Six laboratories performed uniform blank spiked samples with turpentine concentrations of 5.0 μg/L, 100 μg/L and 400 μg/L, respectively The relative standard deviations in the laboratory were 2.1% -8.9%, 2.4% -6.5% and 3.3% -7.9% respectively. The relative standard deviation The standard deviations were 12%, 5.4% and 6.7% respectively. The repeatability limits were 0.6 μg/L, 12.6 μg/L and 49.5 μg/L respectively. The current limits were 1.5 μg/L, 18.2 μg/L and 82.6 μg/L, respectively. Six laboratories separately measured turpentine concentrations of 5.0 μg/L and.200 μg/L of surface water samples. The laboratory phase The standard deviations were 2.1% -4.4% and 3.0% -8.6% respectively. The relative standard deviations of the laboratories were 9.6% and 12%, respectively. The repeatability limits were 0.4 μg/L and 27.8 μg/L, respectively. The reproducibility limits were 1.3 μg/L and 70.8 μg/L, respectively. Six laboratories separately measured the samples of domestic sewage with turpentine concentrations of 50.0 μg/L and 400 μg/L, and the laboratories The relative standard deviations were 2.4% ~ 6.3% and 1.2% ~ 9.8% respectively. The relative standard deviations (RSDs) were 8.7% and 8.3%, respectively. The repeatability limits were 6.5 μg/L and 51.5 μg/L, respectively. The reproducibility limits were 13.0 μg/L and 93.9 μg/L, respectively. 6 laboratories respectively, the turpentine concentrations of 50.0 μg/L and 400 μg/L of industrial wastewater samples were measured, the laboratory The relative standard deviations (RSDs) were 1.7% -9.6% and 1.1% -8.7% respectively. The relative standard deviations (RSDs) were 11% and 15% respectively. The repeatability limits were 8.2 μg/L and 52.5 μg/L, respectively. The reproducibility limits were 16.2 μg/L and 157 μg/L, respectively. 89.2 Accuracy Six laboratories, respectively, spiked with turpentine concentrations of 5.0 μg/L,.200 μg/L of surface water samples were measured, plus the standard The yields were 76.0% -96.0% and 77.9% -112%, respectively. The final recoveries were 88.7% ± 17% and 95.6% ± 23%, respectively. Six laboratories respectively spiked turpentine spiked at a concentration of 50.0 μg/L, 400 μg/L of domestic sewage samples were measured, The recoveries were 88.5% -110% and 77.3% -95.0%, respectively. The final recoveries of spiked samples were 95.6% ± 16% 87.4% ± 14%. Six laboratories respectively measured the spiked industrial wastewater samples with spiked concentrations of 50.0 μg/L and 400 μg/L, The recoveries were 75.9% -106% and 71.1% -109%, respectively. The final recoveries of spiked samples were 91.6% ± 20% 89.2% ± 27%. 10 Quality Assurance and Quality Control 10.1 Instrument Performance Check Perform instrument performance checks prior to or within 24 h of each batch of sample analysis. The resulting 4-Bromofluorobenzene (4.6) key ions Abundance must all meet the criteria in Table 1. 10.2 Initial calibration The calibration curve requires a minimum of 5 concentration series and the correlation coefficient for the initial calibration curve should be ≥0.995 or Relative Response Factor (RRF) The relative standard deviation (RSD) should be ≤ 20%, or should find the cause or redraw the calibration curve. 10.3 Continuous calibration Every 24 h analysis of the calibration curve intermediate concentration point, the measurement results and the actual concentration val......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of HJ 866-2017_English be delivered?Answer: Upon your order, we will start to translate HJ 866-2017_English as soon as possible, and keep you informed of the progress. The lead time is typically 1 ~ 3 working days. 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