Guannan Deng, A. Kan, Z. Dai, A. Lu, K. Harouaka, Yue Zhao, Xin Wang, M. Tomson
{"title":"高钙浓度对120 ~ 220℃高温下硫酸盐结垢预测的影响","authors":"Guannan Deng, A. Kan, Z. Dai, A. Lu, K. Harouaka, Yue Zhao, Xin Wang, M. Tomson","doi":"10.2118/190744-MS","DOIUrl":null,"url":null,"abstract":"\n High Ca concentration up to 40,000 mg/L in produced water was observed in Marcellus shale gas wells, such extremely high concentration have great impact to solubility of sulfate scales. To evaluate this impact, the virial coefficients for Ca-SO4 ion-interaction needs to be quantified in Pitzer equation for different P-T regimes. More solubility data with high Ca concentration at high temperature (>120°C) needs to be experimentally determined.\n The solubility of anhydrite at Ca2+ concentration up to 1 m (mol/kg H2O) from temperature of 120°C to 220°C and at saturated vapor pressure was measured. A stainless-steel pressure proof reactor was designed to contain a Pyrex bottle, in which reagent grade anhydrite powder was mixed with salt solution of 0.25 m, 0.5 m, 0.77 m, and 1 m CaCl2. Sample was taken by using inner pressure to push solution through inline-filter, and then the Ca2+ and SO42- concentrations in the filtrate was determined by inductively coupled plasma optical emission spectrometry (ICP-OES) and compared over time to confirm when solubility equilibrium was reached.\n Results shows that current Pitzer's equation model (ScaleSoftPitzer 2017) predicts saturation index (SI) values with an error of less than 0.1SI at up to 0.77 m Ca2+, but shows an error as much as −0.21 SI at 1 m Ca2+ condition. For typical produced water with less than 30,000 mg/L Ca (about 0.75 m), the current model gives a reliable prediction of anhydrite solubility. If the produced water contains greater than 30,000 mg/L Ca, the model may yield error that are as much as −0.2 SI. Further experiments are needed to correct the Pitzer equation coefficients for better scale predication at higher than 30,000 mg/L Ca.","PeriodicalId":445983,"journal":{"name":"Day 1 Wed, June 20, 2018","volume":"2 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Impact of High Calcium Concentration on Sulfate Scale Prediction at High Temperature from 120°C to 220°C\",\"authors\":\"Guannan Deng, A. Kan, Z. Dai, A. Lu, K. Harouaka, Yue Zhao, Xin Wang, M. Tomson\",\"doi\":\"10.2118/190744-MS\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n High Ca concentration up to 40,000 mg/L in produced water was observed in Marcellus shale gas wells, such extremely high concentration have great impact to solubility of sulfate scales. To evaluate this impact, the virial coefficients for Ca-SO4 ion-interaction needs to be quantified in Pitzer equation for different P-T regimes. More solubility data with high Ca concentration at high temperature (>120°C) needs to be experimentally determined.\\n The solubility of anhydrite at Ca2+ concentration up to 1 m (mol/kg H2O) from temperature of 120°C to 220°C and at saturated vapor pressure was measured. A stainless-steel pressure proof reactor was designed to contain a Pyrex bottle, in which reagent grade anhydrite powder was mixed with salt solution of 0.25 m, 0.5 m, 0.77 m, and 1 m CaCl2. Sample was taken by using inner pressure to push solution through inline-filter, and then the Ca2+ and SO42- concentrations in the filtrate was determined by inductively coupled plasma optical emission spectrometry (ICP-OES) and compared over time to confirm when solubility equilibrium was reached.\\n Results shows that current Pitzer's equation model (ScaleSoftPitzer 2017) predicts saturation index (SI) values with an error of less than 0.1SI at up to 0.77 m Ca2+, but shows an error as much as −0.21 SI at 1 m Ca2+ condition. For typical produced water with less than 30,000 mg/L Ca (about 0.75 m), the current model gives a reliable prediction of anhydrite solubility. If the produced water contains greater than 30,000 mg/L Ca, the model may yield error that are as much as −0.2 SI. 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引用次数: 1
摘要
Marcellus页岩气井采出水中Ca浓度高达40000 mg/L,这种极高的浓度对硫酸盐水垢的溶解度有很大影响。为了评估这种影响,Ca-SO4离子相互作用的维里系数需要在不同的P-T制度的Pitzer方程中量化。更多的高温(bbb120℃)高Ca浓度下的溶解度数据需要通过实验来确定。测定了钙离子浓度为1 m (mol/kg H2O)时硬石膏在120 ~ 220℃和饱和蒸汽压下的溶解度。设计了一个不锈钢耐压反应器,其中装有一个耐热玻璃瓶,将试剂级硬石膏粉末与0.25 m、0.5 m、0.77 m和1 m CaCl2的盐溶液混合。利用内压推动溶液通过内联过滤器,然后用电感耦合等离子体发射光谱法(ICP-OES)测定滤液中的Ca2+和SO42-浓度,并随时间进行比较,以确定何时达到溶解度平衡。结果表明,目前的Pitzer方程模型(ScaleSoftPitzer 2017)预测饱和指数(SI)值在高达0.77 m Ca2+条件下误差小于0.1SI,但在1 m Ca2+条件下误差高达- 0.21 SI。对于Ca含量低于30,000 mg/L(约0.75 m)的典型采出水,目前的模型可以可靠地预测硬石膏的溶解度。如果采出水中Ca含量大于30,000 mg/L,则模型可能产生高达- 0.2 SI的误差。需要进一步的实验来修正Pitzer方程系数,以便在高于30,000 mg/L Ca的情况下更好地预测结垢。
Impact of High Calcium Concentration on Sulfate Scale Prediction at High Temperature from 120°C to 220°C
High Ca concentration up to 40,000 mg/L in produced water was observed in Marcellus shale gas wells, such extremely high concentration have great impact to solubility of sulfate scales. To evaluate this impact, the virial coefficients for Ca-SO4 ion-interaction needs to be quantified in Pitzer equation for different P-T regimes. More solubility data with high Ca concentration at high temperature (>120°C) needs to be experimentally determined.
The solubility of anhydrite at Ca2+ concentration up to 1 m (mol/kg H2O) from temperature of 120°C to 220°C and at saturated vapor pressure was measured. A stainless-steel pressure proof reactor was designed to contain a Pyrex bottle, in which reagent grade anhydrite powder was mixed with salt solution of 0.25 m, 0.5 m, 0.77 m, and 1 m CaCl2. Sample was taken by using inner pressure to push solution through inline-filter, and then the Ca2+ and SO42- concentrations in the filtrate was determined by inductively coupled plasma optical emission spectrometry (ICP-OES) and compared over time to confirm when solubility equilibrium was reached.
Results shows that current Pitzer's equation model (ScaleSoftPitzer 2017) predicts saturation index (SI) values with an error of less than 0.1SI at up to 0.77 m Ca2+, but shows an error as much as −0.21 SI at 1 m Ca2+ condition. For typical produced water with less than 30,000 mg/L Ca (about 0.75 m), the current model gives a reliable prediction of anhydrite solubility. If the produced water contains greater than 30,000 mg/L Ca, the model may yield error that are as much as −0.2 SI. Further experiments are needed to correct the Pitzer equation coefficients for better scale predication at higher than 30,000 mg/L Ca.