Feasibility of Using Periodic Manual Sampling to Achieve Auto Sampling Intentions in Gas Export Measurement System

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Feasibility of Using Periodic Manual Sampling to Achieve Auto Sampling Intentions in Gas Export Measurement System By Anwar Sutan Anwar.Sutan@i-vigilant.com

Background Flow proportional sample has not been reliable enough Issues: Plant shut down Wrong count Grab sampler stops working in the middle Wrong handling Study is performed to see if spot sampling will be sufficient to achieve the intentions of auto sampling system

Why Sampling DECC Measurement Guideline Issue 8 paragraph 6.5.1 Each system should feature a manual sampling point to permit spot samples to be taken when required.

Reasons for Auto Sampling To provide an independent check of the performance of the chromatographs To provide data for the characterisation of components from C6 to C10 To provide data for the additional components present in the gas which the chromatographs are unable to detect To provide analysis data should chromatographs be unavailable due to breakdown or maintenance To provide verification of gas chromatograph

Reason 1 To provide an independent check of the performance of the chromatographs Independent check of GC performance is performed with following method: Yearly ISO 10723 multilevel calibration The use of GC conditional based monitoring tool Spot sampling will provide information on how representative the sample is With spot sampling GC data can be recorded at the same time as the spot sampling time (subject to additional lag time in gas which can be calculated) This will compare the measurement of the same gas with two different methods Similar result is expected when sample conditioning system provides representative sample ISO 10723, GC CBM tool, and spot sampling provides independent check of both gas chromatograph and sampling conditioning system

No Lag Time Spot sampling Analysers Lag time Take the sample at hh:mm Note analysers reading at hh:mm + lag time ± 1 cycle Average analyser reading and compare against spot sampling result Comparison of measurement of the same gas Provide independent check of the performance of pressure let down system

Finding Test on several sites show that heavy end results (i.e. C7+) from spot sampling is significantly higher than GC reading

C7+ from Site 1 GC vs Spot sample: Daily GC average = 0.077 Sample average = 0.194 Difference: 152% Financial Exposure: Lost of roughly 200,000

C7+ from Site 2 GC vs Spot sample: Daily GC average = 0.104 Sample average = 0.247 Difference: 138% Financial Exposure: Lost of roughly 158,000

MONTHLY EXPOSURE > 100,000 LOST in heavy components mis-measurement.

WHY IT HAPPENS Most likely because of liquid drop outs Not enough heating applied in sample let down system High hydrocarbon dewpoint

Reason 2 To provide data for the characterisation of components from C6 to C10 Flow proportional sampling will be the best way of measuring the split, however... If the sensitivity of the split components are very low against the calculation of CV, density, or flow rate uncertainty And if historically, the gas compositions have been fairly stable Spot samplings can provide similar information with less accurate result, however they are compensated by the low sensitivity of the parameters and high stability of gas composition

Split Sensitivity Name Value Unit Name Value Unit n-hexane 0.2220 mol % Methane 86.8250 mol % n-heptane 0.0900 mol % Carbon dioxide 2.6410 mol % n-octane 0.0400 mol % Ethane 5.9890 mol % n-nonane 0.0065 mol % H2S 0.0000 mol % n-decane 0.0000 mol % H2O 0.0000 mol % Propane 2.1060 mol % Total 99.9975 mol % i-butane 0.4150 mol % n-butane 0.7020 mol % Base Temp (Tb) 15.0000 deg C neo-pentane 0.0040 mol % Base pressure (Pb) 1.0133 bara i-pentane 0.2450 mol % Combustion/met. temp. 15/15 degc/degc n-pentane 0.2330 mol % Line Temp (T L ) 58.4500 deg C Nitrogen 0.4790 mol % Line Pressure (P L ) 112.1200 bara Component CV Sensitivity ρ Sensitivity C7 0.0036 0.0048 C8 0.0019 0.0025 C9 0.0003 0.0005

Split Sensitivity Toward CV Component mole Fraction Norm mole fraction Expanded relative uncertainty Coverage factor Standard relative uncertainty Relative Sensitivity E(xi)*S*(xi) Methane 0.8683 0.8687 0.0957 2 0.0478-0.0791-0.0038 Nitrogen 0.0048 0.0048 2.0781 2 1.0391-0.0048-0.0050 CO2 0.0264 0.0264 0.6014 2 0.3007-0.0264-0.0079 Ethane 0.0599 0.0599 0.5668 2 0.2834 0.0358 0.0102 Propane 0.0211 0.0211 1.1273 2 0.5636 0.0269 0.0151 i-butane 0.0042 0.0042 1.0677 2 0.5339 0.0081 0.0043 n-butane 0.0070 0.0070 2.2417 2 1.1208 0.0137 0.0154 neo-pentane 0.0000 0.0000 0.0000 2 0.0000 0.0001 0.00000 i-pentane 0.0025 0.0025 1.4920 2 0.7460 0.0064 0.0048 n-pentane 0.0023 0.0023 1.2807 2 0.6403 0.0061 0.0039 Hexane 0.0022 0.0022 2.4811 2 1.2405 0.0073 0.0091 C7 0.0009 0.0009 3.9137 2 1.9568 0.0036 0.0070 C8 0.0000 0.0000 0.0000 2 0.0000 0.0019 0.0000 C9 0.0000 0.0000 0.0000 2 0.0000 0.0003 0.0000 ISO 6976 N/A N/A 0.1000 2 0.0500 1.0000 0.0500 Combined Standard Uncertainty 0.0580 Coverage Factor (k) 2 Combined Expanded Uncertainty (%) 0.1159 CV absolute uncertainty (MJ/m3) 0.05475

Split Sensitivity Toward CV Expanded relative uncertainty Coverage factor Standard relative uncertainty Relative Sensitivity E(xi)*S*(xi) Component mole Fraction Norm Mol % Methane 0.8683 0.8683 0.0957 2 0.0478-0.0791-0.0038 Nitrogen 0.0048 0.0048 2.0781 2 1.0391-0.0048-0.0050 CO2 0.0264 0.0264 0.6014 2 0.3007-0.0264-0.0079 Ethane 0.0599 0.0599 0.5668 2 0.2834 0.0358 0.0102 Propane 0.0211 0.0211 1.1273 2 0.5636 0.0269 0.0151 i-butane 0.0042 0.0042 1.0677 2 0.5339 0.0081 0.0043 n-butane 0.0070 0.0070 2.2417 2 1.1208 0.0137 0.0154 neo-pentane 0.0000 0.0000 0.0000 2 0.0000 0.0001 0.0000 i-pentane 0.0025 0.0025 1.4920 2 0.7460 0.0064 0.0048 n-pentane 0.0023 0.0023 1.2807 2 0.6403 0.0061 0.0039 Hexane 0.0022 0.0022 2.4811 2 1.2405 0.0073 0.0091 C7 0.0009 0.0009 6.4080 2 3.2040 0.0036 0.0115 C8 0.0004 0.0004 23.0969 2 11.5485 0.0019 0.0216 C9 0.0001 0.0001 40.3490 2 20.1745 0.0003 0.0070 ISO 6976 N/A N/A 0.1000 2 0.0500 1.0000 0.0500 Combined Standard Uncertainty 0.0629 Coverage Factor (k) 2 Combined Expanded Uncertainty (%) 0.1258 CV absolute uncertainty (MJ/m3) 0.05475 Combined Expanded Uncertainty: 0.1159 0.1258 (Δ0.01%)

Split Sensitivity Toward Density Expanded relative Coverage Standard relative Component mole Fraction Norm Mol % uncertainty factor uncertainty Relative Sensitivity E(xi)*S*(xi) Methane 0.8683 0.8687 0.0957 2 0.0478-0.2062-0.0099 Nitrogen 0.0048 0.0048 2.0781 2 1.0391 0.0006 0.0006 CO2 0.0264 0.0264 0.6014 2 0.3007 0.0377 0.0113 Ethane 0.0599 0.0599 0.5668 2 0.2834 0.0544 0.0154 Propane 0.0211 0.0211 1.1273 2 0.5636 0.0416 0.0234 i-butane 0.0042 0.0042 1.0677 2 0.5339 0.0124 0.0066 n-butane 0.0070 0.0070 2.2417 2 1.1208 0.0208 0.0233 neo-pentane 0.0000 0.0000 0.0000 2 0.0000 0.0002 0.0000 i-pentane 0.0025 0.0025 1.4920 2 0.7460 0.0097 0.0072 n-pentane 0.0023 0.0023 1.2807 2 0.6403 0.0094 0.0060 Hexane 0.0022 0.0022 2.4811 2 1.2405 0.0117 0.0145 C7 0.0009 0.0009 3.9137 2 1.9568 0.0048 0.0094 C8 0.0000 0.0000 0.0000 2 0.0000 0.0025 0.0000 C9 0.0000 0.0000 0.0000 2 0.0000 0.0005 0.0000 Pressure 112.12 112.12 0.2500 2 0.1250 1.1048 0.1381 Temperature 58.4500 58.4500 0.8554 2 0.4277-0.3159-0.1351 AGA 8 N/A N/A 0.1000 2 0.0500 1.0000 0.0500 Combined Standard Uncertainty 0.2045 Coverage Factor (k) 2 Combined Expanded Uncertainty (%) 0.4090 Line Density absolute uncertainty (Kg/m3) 0.37603

Split Sensitivity Toward Density Expanded relative Coverage Standard relative Component mole Fraction Norm Mol % uncertainty factor uncertainty Relative Sensitivity E(xi)*S*(xi) Methane 0.8683 0.8683 0.0957 2 0.0478-0.2062-0.0099 Nitrogen 0.0048 0.0048 2.0781 2 1.0391 0.0006 0.0006 CO2 0.0264 0.0264 0.6014 2 0.3007 0.0377 0.0113 Ethane 0.0599 0.0599 0.5668 2 0.2834 0.0544 0.0154 Propane 0.0211 0.0211 1.1273 2 0.5636 0.0416 0.0234 i-butane 0.0042 0.0042 1.0677 2 0.5339 0.0124 0.0066 n-butane 0.0070 0.0070 2.2417 2 1.1208 0.0208 0.0233 neo-pentane 0.0000 0.0000 0.0000 2 0.0000 0.0002 0.0000 i-pentane 0.0025 0.0025 1.4920 2 0.7460 0.0097 0.0072 n-pentane 0.0023 0.0023 1.2807 2 0.6403 0.0094 0.0060 Hexane 0.0022 0.0022 2.4811 2 1.2405 0.0117 0.0145 C7 0.0009 0.0009 6.4080 2 3.2040 0.0048 0.0153 C8 0.0004 0.0004 23.0969 2 11.5485 0.0025 0.0287 C9 0.0001 0.0001 40.3490 2 20.1745 0.0005 0.0093 Pressure 112.12 112.12 0.2500 2 0.1250 1.1048 0.1381 Temperature 58.4500 58.4500 0.8554 2 0.4277-0.3159-0.1351 AGA 8 N/A N/A 0.1000 2 0.0500 1.0000 0.0500 Combined Standard Uncertainty 0.2071 Coverage Factor (k) 2 Combined Expanded Uncertainty (%) 0.4141 Line Density absolute uncertainty (Kg/m3) 0.38076 Combined Expanded Uncertainty: 0.409 0.4141 (Δ0.01%)

Reason 3 Provide data for the additional components present in the gas which the chromatographs are unable to detect Spot sampling and other types analysers (i.e. H2O and H2S analysers) can provide the same information Isentropic Exponent and Dynamic Viscosity has negligible effect to mass flow rate uncertainty

Isentropic Exponent Effect

Viscosity Effect

Reason 4 Provide analysis data should chromatographs be unavailable due to breakdown or maintenance GC historical data can provide better function as it will consist of more up to date data (not data from last month average) Using auto sampler, it uses approximately 6 weeks old actual data

Conclusion All reasons to perform monthly proportional sample can be fulfilled by performing spot sampling (dependent on gas stability) Split determination will be more accurate by performing flow proportional sample, however spot sample can provide similar outcome The lower split accuracy can be justified by the low sensitivity of split parameters toward system uncertainty and the high stability of gas composition It is feasible to fulfil the intention of auto sampling by performing periodic spot sampling

Thank you