地球化学
地毬化學
지구화학
GEOCHIMICA
2014年
6期
647-654
,共8页
稀土元素%分析方法%自生方解石%沉积泥灰岩
稀土元素%分析方法%自生方解石%沉積泥灰巖
희토원소%분석방법%자생방해석%침적니회암
rare earth elements%analytical method%authigenic calcites%sedimentary marls
碳酸盐岩稀土元素是沉积环境示踪的理想参数,但由于自生沉积碳酸盐矿物的稀土元素含量远低于陆源黏土等其他矿物,在样品处理过程中少量陆源黏土矿物的溶解,将影响沉积环境的示踪。因此,如何在样品处理过程中避免陆源黏土矿物中稀土元素的释放,从而获得海洋环境自生沉淀形成的碳酸盐矿物中的元素方法非常重要。本文应用地层中常见的同一泥灰岩样品,分别用5%醋酸、5%盐酸、2%和5%硝酸浸取,采用0.5 h、1 h、2 h、3 h、6 h和24 h的反应时间,用X射线衍射法(XRD)分析酸不溶残渣矿物组成、电感耦合等离子体原子发射光谱法(ICP-AES)测定酸可溶相溶液的主元素和微量元素含量、电感耦合等离子体质谱法(ICP-MS)测定酸可溶相溶液的稀土元素含量,结果表明所有酸溶均可完全溶解泥灰岩中的方解石矿物,并有少量黏土发生溶解,导致稀土总量和Ce/Ce*增高,但对Eu/Eu*、LaN/YbN和Gd/Gd*等参数没有影响。泥灰岩中自生方解石的稀土元素理想溶样条件是5%醋酸反应1 h以内,溶液的ICP-MS分析结果适用于示踪沉积环境的氧化还原条件。
碳痠鹽巖稀土元素是沉積環境示蹤的理想參數,但由于自生沉積碳痠鹽礦物的稀土元素含量遠低于陸源黏土等其他礦物,在樣品處理過程中少量陸源黏土礦物的溶解,將影響沉積環境的示蹤。因此,如何在樣品處理過程中避免陸源黏土礦物中稀土元素的釋放,從而穫得海洋環境自生沉澱形成的碳痠鹽礦物中的元素方法非常重要。本文應用地層中常見的同一泥灰巖樣品,分彆用5%醋痠、5%鹽痠、2%和5%硝痠浸取,採用0.5 h、1 h、2 h、3 h、6 h和24 h的反應時間,用X射線衍射法(XRD)分析痠不溶殘渣礦物組成、電感耦閤等離子體原子髮射光譜法(ICP-AES)測定痠可溶相溶液的主元素和微量元素含量、電感耦閤等離子體質譜法(ICP-MS)測定痠可溶相溶液的稀土元素含量,結果錶明所有痠溶均可完全溶解泥灰巖中的方解石礦物,併有少量黏土髮生溶解,導緻稀土總量和Ce/Ce*增高,但對Eu/Eu*、LaN/YbN和Gd/Gd*等參數沒有影響。泥灰巖中自生方解石的稀土元素理想溶樣條件是5%醋痠反應1 h以內,溶液的ICP-MS分析結果適用于示蹤沉積環境的氧化還原條件。
탄산염암희토원소시침적배경시종적이상삼수,단유우자생침적탄산염광물적희토원소함량원저우륙원점토등기타광물,재양품처리과정중소량륙원점토광물적용해,장영향침적배경적시종。인차,여하재양품처리과정중피면륙원점토광물중희토원소적석방,종이획득해양배경자생침정형성적탄산염광물중적원소방법비상중요。본문응용지층중상견적동일니회암양품,분별용5%작산、5%염산、2%화5%초산침취,채용0.5 h、1 h、2 h、3 h、6 h화24 h적반응시간,용X사선연사법(XRD)분석산불용잔사광물조성、전감우합등리자체원자발사광보법(ICP-AES)측정산가용상용액적주원소화미량원소함량、전감우합등리자체질보법(ICP-MS)측정산가용상용액적희토원소함량,결과표명소유산용균가완전용해니회암중적방해석광물,병유소량점토발생용해,도치희토총량화Ce/Ce*증고,단대Eu/Eu*、LaN/YbN화Gd/Gd*등삼수몰유영향。니회암중자생방해석적희토원소이상용양조건시5%작산반응1 h이내,용액적ICP-MS분석결과괄용우시종침적배경적양화환원조건。
Rare earth elements (REEs) of sedimentary carbonate rocks are the best parameters to trace redox conditions of sedimentary environment. However, because the REE contents of authigenic carbonate minerals are much lower than that of terrigenous clays, a small quantity of terrigenous clays dissolved will affect true redox implication of sedimentary environment. Therefore, it is very important to conduct an analytical method to get the true REE contents of authigenic carbonate minerals deposited in marine environment without the contamination from clays. Here we use 5% CH3COOH, 5% HCl, 2% and 5% HNO3 to dissolve powder samples split from one marls that usually occurred worldwide for 0.5, 1, 2, 3, 6 and 24 hours, respectively. The results of XRD analysis of insoluble residues and ICP-AES and ICP-MS analysis of acid dissolved solution show that calcite was completely dissolved and small quantities of clays were also dissolved. These dissolved clays resulted in an increase of REE contents and Ce/Ce* ratio, but not affect Eu/Eu*, LaN/YbN and Gd/Gd* ratios. The better dissolution method of authigenic calcites of marls is to use 5%CH3COOH to dissolve powder samples for less than 1 hour. The results of ICP-MS analysis of acid dissolved solution are suitable to trace the redox condition of sedimentary environment.