西藏拉萨地体西北部革吉地区两期早白垩世岩浆作用——锆石U-Pb年龄、Hf同位素和地球化学特征

邦巴岩体位于拉萨地块西部革吉地区,由主体花岗岩、花岗闪长岩、闪长质包体及一系列近平行、南北向展布的花岗斑岩脉体组成。野外地质调查和LA-MC-ICP-MS锆石U-Pb定年表明,革吉地区白垩纪的两期岩浆活动分别发生在131~132Ma和127Ma。早期岩浆作用形成主体花岗岩、花岗闪长岩及闪长质包体,具有以下特征:(1)明显富集K、Cs等大离子亲石元素,亏损Nb、Ti、Zr等高场强元素;(2)具有明显的负Eu异常(Eu/Eu*=0.49~0.61)及负Ce异常;(3)具负εHf(t)值(-3.2~-0.3)及古老的地壳模式年龄(1.210~1.399Ga);(4)初始Sr同位素比值为0.70424~0.71472,εHf(t)值为-5.70~-5.54。晚期岩浆作用形成花岗斑岩脉体,具有以下特征:(1)富集K、Cs等大离子亲石元素,强烈亏损Nb、Ta、Ti等高场强元素;(2)基本不具有负Eu异常或具有轻微的负Eu异常(Eu/Eu*=0.74~0.87);(3)具有更老的Hf同位素地壳模式年龄(1.226~1.576Ga)及更负的大范围变化的εHf(t)值(-6.1~-0.7)。晚期岩浆作用锆饱和温度(777~796℃)及轻稀土元素不饱和温度(794~812℃)均高于早期岩浆的锆饱和温度(661~762℃)及轻稀土元素不饱和温度(750~769℃)。上述特征表明,两期岩浆作用均为中拉萨地块古老基底部分与地幔物质混染部分熔融的产物,随着岩浆作用的持续进行,岩浆中的古老地壳组分增加,熔体温度也增加,可能与南向俯冲的班公-怒江洋壳回转驱动的地幔岩浆活动向北迁移有关。     

Impacts of mineralogical compositions on different trapping mechanisms during long-term CO<Subscript>2</Subscript> storage in deep saline aquifers

Deep saline aquifers in sedimentary basins are considered to have the greatest potential for CO₂ geological storage in order to reduce carbon emissions. CO₂ injected into a saline sandstone aquifer tends to migrate upwards toward the caprock because the density of the supercritical CO₂ phase is lower than that of formation water. The accumulated CO₂ in the upper portions of the reservoir gradually dissolves into brine, lowers pH and changes the aqueous complexation, whereby induces mineral alteration. In turn, the mineralogical composition could impose significant effects on the evolution of solution, further on the mineralized CO₂. The high density of aqueous phase will then move downward due to gravity, give rise to “convective mixing,” which facilitate the transformation of CO₂ from the supercritical phase to the aqueous phase and then to the solid phase. In order to determine the impacts of mineralogical compositions on trapping amounts in different mechanisms for CO₂ geological storage, a 2D radial model was developed. The mineralogical composition for the base case was taken from a deep saline formation of the Ordos Basin, China. Three additional models with varying mineralogical compositions were carried out. Results indicate that the mineralogical composition had very obvious effects on different CO₂ trapping mechanisms. Specific to our cases, the dissolution of chlorite provided Mg²⁺ and Fe²⁺ for the formation of secondary carbonate minerals (ankerite, siderite and magnesite). When chlorite was absent in the saline aquifer, the dominant secondary carbon sequestration mineral was dawsonite, and the amount of CO₂ mineral trapping increased with an increase in the concentration of chlorite. After 3000 years, 69.08, 76.93, 83.52 and 87.24 % of the injected CO₂ can be trapped in the solid (mineral) phase, 16.05, 11.86, 8.82 and 6.99 % in the aqueous phase, and 14.87, 11.21, 7.66 and 5.77 % in the gas phase for Case 1 through 4, respectively.