化工学报
化工學報
화공학보
JOURNAL OF CHEMICAL INDUSY AND ENGINEERING (CHINA)
2015年
5期
1861-1866
,共6页
王擎%黄宗越%迟铭书%石聚欣%王智超%隋义
王擎%黃宗越%遲銘書%石聚訢%王智超%隋義
왕경%황종월%지명서%석취흔%왕지초%수의
干酪根%固体核磁%红外光谱%化学结构
榦酪根%固體覈磁%紅外光譜%化學結構
간락근%고체핵자%홍외광보%화학결구
oil shale kerogen%solid state13C NMR%FT-IR spectroscopy%chemical structure
利用先进的测试技术对5种不同地区的油页岩干酪根分别进行XRD、13C NMR与FT-IR分析,获得重要结构信息。通过XRD检测分析,确定5种干酪根以长程无序的聚合状态存在。采用13C NMR技术表征出干酪根的碳原子化学结构,并获得碳骨架结构的18个重要参数。最后利用 FT-IR 技术对干酪根官能团进行定性分析,与13C NMR实验结果互相验证,得到干酪根化学结构的详细信息。结果表明:油页岩干酪根脂碳结构最多,高达60%~90%。其中又以亚甲基碳为主,有77%~90%,且多数为直链结构,脂环或支链结构较少。芳碳结构除桦甸以单环为主外,其余均为单环和多环结构并存,其中多环结构以迫位缩合为主。氧结构总体以碳氧单键(醇、酚或醚基)和CO两种形式存在,其中羧基类CO多于羰基类CO。变质程度低的干酪根中存在较多CO,而高变质程度的干酪根则以碳氧单键C O为主。
利用先進的測試技術對5種不同地區的油頁巖榦酪根分彆進行XRD、13C NMR與FT-IR分析,穫得重要結構信息。通過XRD檢測分析,確定5種榦酪根以長程無序的聚閤狀態存在。採用13C NMR技術錶徵齣榦酪根的碳原子化學結構,併穫得碳骨架結構的18箇重要參數。最後利用 FT-IR 技術對榦酪根官能糰進行定性分析,與13C NMR實驗結果互相驗證,得到榦酪根化學結構的詳細信息。結果錶明:油頁巖榦酪根脂碳結構最多,高達60%~90%。其中又以亞甲基碳為主,有77%~90%,且多數為直鏈結構,脂環或支鏈結構較少。芳碳結構除樺甸以單環為主外,其餘均為單環和多環結構併存,其中多環結構以迫位縮閤為主。氧結構總體以碳氧單鍵(醇、酚或醚基)和CO兩種形式存在,其中羧基類CO多于羰基類CO。變質程度低的榦酪根中存在較多CO,而高變質程度的榦酪根則以碳氧單鍵C O為主。
이용선진적측시기술대5충불동지구적유혈암간락근분별진행XRD、13C NMR여FT-IR분석,획득중요결구신식。통과XRD검측분석,학정5충간락근이장정무서적취합상태존재。채용13C NMR기술표정출간락근적탄원자화학결구,병획득탄골가결구적18개중요삼수。최후이용 FT-IR 기술대간락근관능단진행정성분석,여13C NMR실험결과호상험증,득도간락근화학결구적상세신식。결과표명:유혈암간락근지탄결구최다,고체60%~90%。기중우이아갑기탄위주,유77%~90%,차다수위직련결구,지배혹지련결구교소。방탄결구제화전이단배위주외,기여균위단배화다배결구병존,기중다배결구이박위축합위주。양결구총체이탄양단건(순、분혹미기)화CO량충형식존재,기중최기류CO다우탄기류CO。변질정도저적간락근중존재교다CO,이고변질정도적간락근칙이탄양단건C O위주。
Five different oil shale kerogens were analyzed with advanced testing techniques (XRD,13C NMR and FT-IR) to obtain important structural information. The long-range disordered state of aggregation was also confirmed by XRD. Using13C NMR spectroscopy, 18 characteristic parameters of carbon skeleton structure were obtained. Detailed information about the chemical structure of kerogen was obtained through verifying the results of13C NMR experiments with the qualitative analysis of kerogen groups made by FT-IR technique. The aliphatic structure of oil shale kerogen was up to 60%—90%, with the methylene carbon occupying the dominant position of 77%—90%, and most of the aliphatic structure were straight-chain while less alicyclic or branched chain. In addition to Huadian oil shale with a monocyclic aromatic carbon structure, the other four oil shale kerogens were co-existing monocyclic and polycyclic rings, with the latter mainly peri-condensed. The oxygen structure was CO (alcohol, phenol, ether) and CO, and carboxyl class was more than carbonyl class CO. More CO in kerogen was due to a low degree of metamorphism, while a high degree of metamorphism resulted in more CO.