石油与天然气地质 ›› 2015, Vol. 36 ›› Issue (2): 183-192.doi: 10.11743/ogg20150202

• 油气地质 • 上一篇    下一篇

川东北地区长兴组酸性气藏中硫化氢来源及成因

李开开1, 蔡春芳2, 姜磊2, 贺训云3, 黄政4   

  1. 1. 中国地质大学 能源学院, 北京 100083;
    2. 中国科学院 地质与地球物理研究所 油气资源研究重点实验室, 北京 100029;
    3. 中国石油 杭州地质研究院 中国石油天然气集团公司碳酸盐岩储层重点实验室, 浙江 杭州 310023;
    4. 中国石油 冀东油田分公司, 河北 唐山 063000
  • 收稿日期:2014-03-31 修回日期:2014-12-20 出版日期:2015-04-08 发布日期:2015-05-13
  • 作者简介:李开开(1983-),男,讲师,碳酸盐岩储层与流体-岩石相互作用.E-mail:93445190@qq.com.
  • 基金资助:
    国家杰出青年科学基金项目(41125009);国家自然科学基金青年科学基金项目(41202108).

Origin of H2S in sour gas reservoirs in the Upper Permian Changxing Formation in northeastern Sichuan Basin

Li Kaikai1, Cai Chunfang2, Jiang Lei2, He Xunyun3, Huang Zheng4   

  1. 1. Energy Resource Department, China University of Geosciences, Beijing 100083, China;
    2. Key Lab of Petroleum Resources Research, Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing 100029, China;
    3. Key Laboratory of Carbonate Reservoirs, PetroChina Hangzhou Research Institute of Geology, CNPC, Hangzhou, Zhejiang 310023, China;
    4. PetroChina Jidong Oilfield Company, Tangshan, Hebei 063000, China
  • Received:2014-03-31 Revised:2014-12-20 Online:2015-04-08 Published:2015-05-13

摘要: 川东北地区长兴组(P3ch)和飞仙关组(T1f)天然气藏中检测出的高浓度H2S气体目前被认为是硫酸盐热化学还原作用(TSR)成因。然而,长兴组内并无类似于飞仙关组的膏岩层或硬石膏结核发育,因此长兴组气藏的酸化过程成疑。通过针对研究区地层古压力以及输导体系方面的探讨,并结合碳酸盐岩晶格硫酸盐(CAS)含量、同位素以及稀土微量元素分析,研究认为:①长兴组气藏中高浓度H2S气体不太可能由飞仙关组酸性气藏“倒灌”形成,而是由本地地层中发生的TSR作用所导致;②嘉陵江组(T1j)和黄龙组(C2h)沉积时期蒸发性卤水以及长兴期海水并非主要来源,而飞仙关期蒸发性卤水的倒灌为长兴组TSR反应的发生提供了主要的SO42-来源,并导致其内的TSR成因方解石具有与飞仙关组方解石相似的正Eu异常、高Sr(高达7 767×10-6)和Ba含量(高达1 279×10-6)以及相对同时期海水较高的87Sr/86Sr比值(0.707 24~0.707 55);③卤水穿层流动主要发生于沉积期或成岩早期,沉积-准同生期渗透回流作用和早-中埋藏阶段差异压实作用为卤水运移的主要机制;④长兴组白云岩化过程中释放的CAS也可能是重要的SO42-来源,并导致该层位气藏中H2S及储层沥青δ34S值较飞仙关组略有偏负。

关键词: 晶格硫酸盐, 差异压实, 硫酸盐热化学还原反应, 硫化氢, 酸性气藏, 长兴组, 川东北地区

Abstract: High H2S concentrations found in gas reservoirs within the Upper Permian Changxing Fm(P3ch)and Lower Triassic Feixianguan Fm(T1f)are generally thought to be formed via a process known as thermochemical sulfate reduction(TSR).However,unlike the T1f Fm,rare gypsum/anhydrite beds or anhydrite nodular were found in the P3ch Fm.This cast doubts over the accepted model for the souring process of the P3ch reservoirs.This study provides an analysis of palaegeopressure and carrier system within this system using carbonate-associated sulfate(CAS),isotopes,trace and rare earth element data.Results shows that,the H2S of high concentrations within the P3ch reservoirs were not derived from downward migration of sour gas from the T1f Fm,but were generated in situ through TSR;reactive sulfates were mainly derived from cross-formational brines migration from the T1f Fm,but with insignificant contributions from the Late Permian P3ch seawater and sulfate-rich brines within the Lower Triassic Jialingjiang Fm and Middle Carboniferous Honglong Fm formations,and the down-migration of T1f brines may have resulted in the P3ch TSR calcites having positive Eu anomaly,high Sr contents(up to 7 767 ppm)and Ba contents(up to 1 279 ppm)close to the T1f TSR calcite,and 87Sr/86Sr ratios(0.707 24~0.707 55)more radiogenic than those of the late Permian seawater;the cross-formational brine flow mainly occurred during sedimentary stage or the early stages of diagenesis,and seepage reflux during contemporaneous-penecontemporaneous stage and differential compaction flux during early-mid burial stage might serve as the main migration mechanisms;④CAS released during dolomization was another possible sulfate source,which brought the δ34S values of H2S and bitumen a little lower than those of the T1f Fm.

Key words: CAS, differential compaction, TSR, H2S, sour gas reservoir, Changxing Formation, northeastern Sichuan Basin

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