SO2(g)在水中的溶液和二氧化硫水溶液的热力学。

R N Goldberg, V B Parker
{"title":"SO2(g)在水中的溶液和二氧化硫水溶液的热力学。","authors":"R N Goldberg,&nbsp;V B Parker","doi":"10.6028/jres.090.024","DOIUrl":null,"url":null,"abstract":"<p><p>A consistent set of thermochemical property values, Δ <sub><i>f</i></sub> <i>H</i>°, Δ <sub><i>f</i></sub> <i>G</i>°, <i>S</i>°, and <math> <mrow><msubsup><mi>C</mi> <mi>p</mi> <mi>o</mi></msubsup> </mrow> </math> , at 298.15 K is given for the known constituents of aqueous sulfur dioxide ( <math> <mrow> <msubsup><mrow><mtext>SO</mtext></mrow> <mn>2</mn> <mn>0</mn></msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , <math> <mrow> <msubsup><mrow><mtext>HSO</mtext></mrow> <mn>3</mn> <mo>-</mo></msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , <math> <mrow> <msubsup><mrow><mtext>SO</mtext></mrow> <mn>3</mn> <mrow><mn>2</mn> <mo>-</mo></mrow> </msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , H<sup>+</sup>(aq), and <math> <mrow><msub><mtext>S</mtext> <mn>2</mn></msub> <msubsup><mtext>O</mtext> <mn>5</mn> <mrow><mn>2</mn> <mo>-</mo></mrow> </msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> ). Also tabulated are values of the mean ionic activity coefficients, osmotic coefficients, partial pressure of SO<sub>2</sub>(g), and the relative apparent molar enthalpy as a function of concentration of SO<sub>2</sub>(aq) at 298.15 K. The data analysis considered a wide variety of measurement techniques: calorimetric enthalpies of solution and reaction, heat capacities, equilibrium constants, solubilities, and vapor pressure measurements, both partial and total, over aqueous solutions of SO<sub>2</sub> for the temperature range 278 to 393 K. All auxiliary data have been taken from the most recent set of CODATA values which were converted to a standard state pressure of one bar (0.1 MPa). For the process <math> <mrow> <msub><mrow><mtext>SO</mtext></mrow> <mn>2</mn></msub> <mo>(</mo> <mtext>g</mtext> <mo>)</mo> <mo>=</mo> <msubsup><mrow><mtext>SO</mtext></mrow> <mn>2</mn> <mn>0</mn></msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , the selected \"best\" values are: <i>K</i> = 1.23±0.05 mol kg<sup>-1</sup> bar<sup>-1</sup>, Δ<i>G</i>° = -0.5±0.10 kJ mol<sup>-1</sup>, Δ<i>H</i>° = -26.97±0.30 kJ mol<sup>-1</sup>, and <math><mrow><mi>Δ</mi> <msubsup><mi>C</mi> <mi>p</mi> <mi>o</mi></msubsup> <mo>=</mo> <mn>155</mn> <mo>±</mo> <mn>10</mn> <mspace></mspace> <mtext>J</mtext> <mspace></mspace> <msup><mrow><mtext>mol</mtext></mrow> <mrow><mo>-</mo> <mn>1</mn></mrow> </msup> <mspace></mspace> <msup><mtext>K</mtext> <mrow><mo>-</mo> <mn>1</mn></mrow> </msup> </mrow> </math> . The standard state partial molar entropy of <math> <mrow> <msubsup><mrow><mtext>SO</mtext></mrow> <mn>3</mn> <mrow><mn>2</mn> <mo>-</mo></mrow> </msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , obtained by the analysis of data via two independent thermodynamic pathways is -15.40±0.80 J mol<sup>-1</sup> K<sup>-l</sup> at 298.15 K. Parameters are given which extend the predictions to temperatures up to 373 K.</p>","PeriodicalId":93321,"journal":{"name":"Journal of research of the National Bureau of Standards (1977)","volume":"90 5","pages":"341-358"},"PeriodicalIF":0.0000,"publicationDate":"1985-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658418/pdf/jres-90-341.pdf","citationCount":"85","resultStr":"{\"title\":\"Thermodynamics of Solution of SO<sub>2</sub>(g) in Water and of Aqueous Sulfur Dioxide Solutions.\",\"authors\":\"R N Goldberg,&nbsp;V B Parker\",\"doi\":\"10.6028/jres.090.024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A consistent set of thermochemical property values, Δ <sub><i>f</i></sub> <i>H</i>°, Δ <sub><i>f</i></sub> <i>G</i>°, <i>S</i>°, and <math> <mrow><msubsup><mi>C</mi> <mi>p</mi> <mi>o</mi></msubsup> </mrow> </math> , at 298.15 K is given for the known constituents of aqueous sulfur dioxide ( <math> <mrow> <msubsup><mrow><mtext>SO</mtext></mrow> <mn>2</mn> <mn>0</mn></msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , <math> <mrow> <msubsup><mrow><mtext>HSO</mtext></mrow> <mn>3</mn> <mo>-</mo></msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , <math> <mrow> <msubsup><mrow><mtext>SO</mtext></mrow> <mn>3</mn> <mrow><mn>2</mn> <mo>-</mo></mrow> </msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , H<sup>+</sup>(aq), and <math> <mrow><msub><mtext>S</mtext> <mn>2</mn></msub> <msubsup><mtext>O</mtext> <mn>5</mn> <mrow><mn>2</mn> <mo>-</mo></mrow> </msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> ). Also tabulated are values of the mean ionic activity coefficients, osmotic coefficients, partial pressure of SO<sub>2</sub>(g), and the relative apparent molar enthalpy as a function of concentration of SO<sub>2</sub>(aq) at 298.15 K. The data analysis considered a wide variety of measurement techniques: calorimetric enthalpies of solution and reaction, heat capacities, equilibrium constants, solubilities, and vapor pressure measurements, both partial and total, over aqueous solutions of SO<sub>2</sub> for the temperature range 278 to 393 K. All auxiliary data have been taken from the most recent set of CODATA values which were converted to a standard state pressure of one bar (0.1 MPa). For the process <math> <mrow> <msub><mrow><mtext>SO</mtext></mrow> <mn>2</mn></msub> <mo>(</mo> <mtext>g</mtext> <mo>)</mo> <mo>=</mo> <msubsup><mrow><mtext>SO</mtext></mrow> <mn>2</mn> <mn>0</mn></msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , the selected \\\"best\\\" values are: <i>K</i> = 1.23±0.05 mol kg<sup>-1</sup> bar<sup>-1</sup>, Δ<i>G</i>° = -0.5±0.10 kJ mol<sup>-1</sup>, Δ<i>H</i>° = -26.97±0.30 kJ mol<sup>-1</sup>, and <math><mrow><mi>Δ</mi> <msubsup><mi>C</mi> <mi>p</mi> <mi>o</mi></msubsup> <mo>=</mo> <mn>155</mn> <mo>±</mo> <mn>10</mn> <mspace></mspace> <mtext>J</mtext> <mspace></mspace> <msup><mrow><mtext>mol</mtext></mrow> <mrow><mo>-</mo> <mn>1</mn></mrow> </msup> <mspace></mspace> <msup><mtext>K</mtext> <mrow><mo>-</mo> <mn>1</mn></mrow> </msup> </mrow> </math> . The standard state partial molar entropy of <math> <mrow> <msubsup><mrow><mtext>SO</mtext></mrow> <mn>3</mn> <mrow><mn>2</mn> <mo>-</mo></mrow> </msubsup> <mo>(</mo> <mtext>aq</mtext> <mo>)</mo></mrow> </math> , obtained by the analysis of data via two independent thermodynamic pathways is -15.40±0.80 J mol<sup>-1</sup> K<sup>-l</sup> at 298.15 K. Parameters are given which extend the predictions to temperatures up to 373 K.</p>\",\"PeriodicalId\":93321,\"journal\":{\"name\":\"Journal of research of the National Bureau of Standards (1977)\",\"volume\":\"90 5\",\"pages\":\"341-358\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1985-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658418/pdf/jres-90-341.pdf\",\"citationCount\":\"85\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of research of the National Bureau of Standards (1977)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.6028/jres.090.024\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of research of the National Bureau of Standards (1977)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.6028/jres.090.024","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 85

摘要

给出了已知二氧化硫水溶液组分(SO2 0(aq)、HSO3-(aq。表中还列出了298.15K下作为SO2(aq)浓度函数的平均离子活性系数、渗透系数、SO2分压(g)和相对表观摩尔焓的值。数据分析考虑了多种测量技术:溶液和反应的量热焓、热容、平衡常数、溶解度,以及在278至393K的温度范围内对SO2水溶液的部分和全部蒸汽压测量。所有辅助数据都取自最近的一组CODATA值,这些值被转换为一巴(0.1MPa)的标准状态压力。对于工艺SO2(g)=SO2 0(aq),选择的“最佳”值为:K=1.23±0.05 mol kg-1 bar-1,Δg°=-0.5±0.10 kJ mol-1,ΔH°=-26.97±0.30 kJ mol-2,ΔC p o=155±10 J mol-1 K-1。通过两个独立的热力学途径分析数据,得到了在298.15K时SO3-(aq)的标准态偏摩尔熵为-15.40±0.80J mol-1K-l。给出了将预测扩展到373K温度的参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Thermodynamics of Solution of SO2(g) in Water and of Aqueous Sulfur Dioxide Solutions.

A consistent set of thermochemical property values, Δ f H°, Δ f G°, S°, and C p o , at 298.15 K is given for the known constituents of aqueous sulfur dioxide ( SO 2 0 ( aq ) , HSO 3 - ( aq ) , SO 3 2 - ( aq ) , H+(aq), and S 2 O 5 2 - ( aq ) ). Also tabulated are values of the mean ionic activity coefficients, osmotic coefficients, partial pressure of SO2(g), and the relative apparent molar enthalpy as a function of concentration of SO2(aq) at 298.15 K. The data analysis considered a wide variety of measurement techniques: calorimetric enthalpies of solution and reaction, heat capacities, equilibrium constants, solubilities, and vapor pressure measurements, both partial and total, over aqueous solutions of SO2 for the temperature range 278 to 393 K. All auxiliary data have been taken from the most recent set of CODATA values which were converted to a standard state pressure of one bar (0.1 MPa). For the process SO 2 ( g ) = SO 2 0 ( aq ) , the selected "best" values are: K = 1.23±0.05 mol kg-1 bar-1, ΔG° = -0.5±0.10 kJ mol-1, ΔH° = -26.97±0.30 kJ mol-1, and Δ C p o = 155 ± 10 J mol - 1 K - 1 . The standard state partial molar entropy of SO 3 2 - ( aq ) , obtained by the analysis of data via two independent thermodynamic pathways is -15.40±0.80 J mol-1 K-l at 298.15 K. Parameters are given which extend the predictions to temperatures up to 373 K.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The Temperature Dependence of Spectral Broadening in the Hg (61S0-63P1) Multiplet At High Optical Densities. Absolute Isotopic Abundance Ratio And Atomic Weight Of a Reference Sample of Gallium. Thermal Expansion of Platinum And Platinum-Rhodium Alloys. The Triple Point of Oxygen In Sealed Transportable Cells. A Multi-kilogram Capacity Calorimeter For Heterogeneous Materials.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1