کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6637633 | 461154 | 2014 | 12 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Analysis of some coal-related model compounds and coal derivates with atmospheric solids analysis probe mass spectrometer
ترجمه فارسی عنوان
تجزیه و تحلیل برخی ترکیبات مرتبط با ذغال سنگ و مشتقات زغال سنگ با تجزیه و تحلیل جامدات جامد تجزیه و تحلیل جرم طیف سنج
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کلمات کلیدی
تجزیه و تحلیل مواد جامدات اتمسفری، ترکیبات مرتبط با زغال سنگ، مشتقات زغال سنگ، اوراق قرضه پل مسیر یونیزاسیون،
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
مهندسی شیمی (عمومی)
چکیده انگلیسی
A series of coal-related model compounds (CRMCs) were analyzed with an atmospheric solids analysis probe/time of flight-mass spectrometer (ASAP/TOF-MS). Pyrene, anthracene, and phenanthrene were ionized to generate stable radical molecular cation (M+
- ) and protonated molecular cation ([M+H]+). The ratio of [M+H]+ to M+
- is positively related to the superdelocalizability of the condensed arenes (CAs), indicating that the CA ionizations rely on the intrinsic reactivities of the CA to a certain extent. Fragmental ions were formed via cleavage and/or rearrangement of [M+H]+/M+
- from bridged bond-containing CRMCs during ASAP/TOF-MS analysis. Their formation is related to drying gas temperature and the stabilities of fragmental species. Using ASAP/TOF-MS, a reaction mixture from di(1-naphthyl)methane hydrocracking was directly and rapidly analyzed, and as coal derivates succinic acid and polymethyl benzenepolycarboxylates were identified in the water-soluble portions from a coal and char oxidation within short time, respectively. The fact suggests that ASAP/TOF-MS could be used for real-time monitoring organic mixtures during the reactions of CRMCs and coal conversion.
- ) and protonated molecular cation ([M+H]+). The ratio of [M+H]+ to M+
- is positively related to the superdelocalizability of the condensed arenes (CAs), indicating that the CA ionizations rely on the intrinsic reactivities of the CA to a certain extent. Fragmental ions were formed via cleavage and/or rearrangement of [M+H]+/M+
- from bridged bond-containing CRMCs during ASAP/TOF-MS analysis. Their formation is related to drying gas temperature and the stabilities of fragmental species. Using ASAP/TOF-MS, a reaction mixture from di(1-naphthyl)methane hydrocracking was directly and rapidly analyzed, and as coal derivates succinic acid and polymethyl benzenepolycarboxylates were identified in the water-soluble portions from a coal and char oxidation within short time, respectively. The fact suggests that ASAP/TOF-MS could be used for real-time monitoring organic mixtures during the reactions of CRMCs and coal conversion.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Fuel - Volume 128, 15 July 2014, Pages 302-313
Journal: Fuel - Volume 128, 15 July 2014, Pages 302-313
نویسندگان
Yu-Gao Wang, Xian-Yong Wei, Jing Liu, Zhan-Ku Li, Shou-Ze Wang, Ying-Hua Wang, Guo-Jun Kang, Xing Fan, Zhi-Min Zong,