Operando potassium K-edge X-ray absorption spectroscopy: investigating potassium catalysts during soot oxidation

文献情報

出版日 2020-07-02
DOI 10.1039/D0CP01227K
インパクトファクター 3.676
著者

Catherine J. Davies, Alexander Mayer, Jess Gabb, Jake M. Walls, Volkan Degirmenci, Giannantonio Cibin, Stan Golunski, Simon A. Kondrat


原文を見る

要旨

The chemical and structural nature of potassium compounds involved in catalytic soot oxidation have been studied by a combination of temperature programmed oxidation and operando potassium K-edge X-ray absorption spectroscopy experiments. These experiments are the first known operando studies using tender X-rays (∼3.6 keV) under high temperature oxidation reaction conditions. X-ray absorption near edge structure analysis of K2CO3/Al2O3 catalysts during heating shows that, at temperatures between 100 and 200 °C, potassium species undergo a structural change from an initial hydrated K2CO3·xH2O and KHCO3 mixture to well-defined K2CO3. As the catalyst is heated from 200 °C to 600 °C, a feature associated with multiple scattering shifts to lower energy, indicating increased K2CO3 dispersion, due to its mobility at high reaction temperature. This shift was noted to be greater in samples containing soot than in control experiments without soot and can be attributed to enhanced mobility of the K2CO3, due to the interaction between soot and potassium species. No potassium species except K2CO3 could be defined during reactions, which excludes a potential reaction mechanism in which carbonate ions are the active soot-oxidising species. Simulations of K-edge absorption near edge structures were performed to rationalise the observed changes seen. Findings showed that cluster size, unit cell distortions and variation in the distribution of potassium crystallographic sites influenced the simulated spectra of K2CO3. While further simulation studies are required for a more complete understanding, the current results support the hypothesis that changes in the local structure on dispersion can influence the observed spectra. Ex situ characterisation was carried out on the fresh and used catalyst, by X-ray diffraction and X-ray photoelectron spectroscopy, which indicated changes to the carbonate species, in line with the X-ray absorption spectroscopy experiments.

関連文献

Exploiting isolobal relationships to create new ionic liquids: novel room-temperature ionic liquids based upon (N-alkylimidazole)(amine)BH2+ “boronium” ions

Phillip A. Fox, Scott T. Griffin, W. Matthew Reichert, E. Alan Salter, Ashley B. Smith, Morgan D. Tickell, Benjamin F. Wicker, Eugene A. Cioffi, Robin D. Rogers, Andrzej Wierzbicki

2005-06-16 Communication

DOI: 10.1039/B504631A

Single-crystalline Sb-doped SnO2nanowires: synthesis and gas sensor application

Q. Wan, T. H. Wang

2005-06-23 Communication

DOI: 10.1039/B504094A

Doubly ortho-linked quinoxaline/triarylamine hybrid as a bifunctional, dipolar electroluminescent template for optoelectronic applications

Chien-Tien Chen, Jin-Sheng Lin, Murthy V. R. K. Moturu, Yi-Wen Lin, Wei Yi, Yu-Tai Tao, Chin-Hsiung Chien

2005-07-08 Communication

DOI: 10.1039/B506409K

Regioselective synthesis and zone selective deprotection of [60]fullerene tris-adducts with an e,e,e addition pattern

Florian Beuerle, Nikos Chronakis, Andreas Hirsch

2005-06-16 Communication

DOI: 10.1039/B504748J

Catalytic C–C bond cleavage and C–Si bond formation in the reaction of RCN with Et3SiH promoted by an iron complex

Hiroshi Nakazawa, Kouji Kamata, Masumi Itazaki

2005-07-12 Communication

DOI: 10.1039/B504131G

Noncatalytic mono-N-methylation of aniline in supercritical methanol: the kinetics and acid/base effect

Yoshihiro Takebayashi, Yoshinori Morita, Hideki Sakai, Masahiko Abe, Satoshi Yoda, Takeshi Furuya, Tsutomu Sugeta, Katsuto Otake

2005-07-07 Communication

DOI: 10.1039/B504050G

Highly regio-, chemo- and diastereoselective synthesis of oxa-bridged spirocycles: A novel observation of reverse selectivity

Sengodagounder Muthusamy, Janagiraman Krishnamurthi, Munirathnam Nethaji

2005-06-21 Communication

DOI: 10.1039/B504692K

Co-transport of H+/Cl− by a synthetic prodigiosin mimic

Philip A. Gale, Mark E. Light, Beth McNally, Korakot Navakhun, Kate E. Sliwinski, Bradley D. Smith

2005-05-25 Communication

DOI: 10.1039/B503906A

A potential and ion switched molecular photonic logic gate

Carlo Bignozzi, Hugh Doyle, Gareth Redmond

2005-07-08 Communication

DOI: 10.1039/B507021J

The important role of solvent vapor in an organic solid state reaction

Seiken Nakamatsu, Shinji Toyota, William Jones, Fumio Toda

2005-07-01 Communication

DOI: 10.1039/B503922C

こちらもおすすめ

化合物よくある質問

2-メトキシ-4-(メチルスルフィニル)アミンの主な用途は何ですか?

2-メトキシ-4-(メチルスルフィニル)アミンは、主に医薬品および農薬の製造に使用されます。また、合成化学の一部として研究用材料としても利用されます。

41608-73-52-Methoxy-4-(methyls...
化合物よくある質問

4-溴甲基-3-甲氧基苯甲酸は安全ですか?

安全ではありません。触覚や吸入に注意が必要で、適切な防護具を使用してください。

118684-13-24-(Bromomethyl)-3-me...
化合物よくある質問

4,6-二氯-N-甲基ピラミジンアミンの代替品はありますか?

代替品としては、4,6-二クロロピラミジンアミンや他のピラミジン系化合物が考えられます。ただし、目的と用途によって最適な代替品は異なります。

10397-15-64,6-Dichloro-N-methy...
化合物よくある質問

6-氯-4-甲基-1H-吲哚を含む廃棄物はどのように処理すべきですか?

6-氯-4-甲基-1H-吲哚の廃棄物は、適切な容器に収集し、密閉して保管します。温度は常温、湿度は低く、直射日光を避けて保管することを推奨します。廃棄処理は専門...

885520-84-36-chloro-4-methyl-1H...
化合物よくある質問

2-フローユロ-4-(トリフルオロメチル)ベンゾイドについて「に適用される法規ガイドラインは何ですか」

2-フローユロ-4-(トリフルオロメチル)ベンゾイドのCAS番号は207974-08-1です。この化合物はGHS分類で毒性物質と有害な反応物質として分類されます...

207974-08-1[2-Fluoro-4-(trifluo...
化合物よくある質問

4-ニトロフェニルN-[(ベンゼルオキシルカーボンイル]グリシングリシングリシン酸はどのように保存すればよいですか?

4-ニトロフェニルN-[(ベンゼルオキシルカーボンイル]グリシングリシングリシン酸は、室温で暗所に保管し、乾燥した環境で保存することを推奨します。容器は密閉性の...

19811-64-44-Nitrophenyl N-[(be...
化合物よくある質問

イソデスロラタドリンの代替品はありますか?

イソデスロラタドリンの代替品としては、デスロラタドリンや他の抗ヒスタミン薬が挙げられます。具体的には、デスロラタドリン、ラセカミド、フェルタドリンなどが、症状や...

183198-49-4Iso Desloratadine
化合物よくある質問

5-甲氧基-1,2,3,4-四氢异喹啉盐酸盐はどのように合成されますか?

5-甲氧基-1,2,3,4-四氢异喹啉盐酸盐の一般的な合成方法は、メタノール中で5-メトキシ-1,2,3,4-四ヒュドロイソキシンを塩酸で塩化します。この反応で...

103030-69-95-Methoxy-1,2,3,4-te...
化合物よくある質問

4-アミノ-5-メトキシ-2-トルエンサルホニック酸についての法規ガイドラインは何ですか?

CAS番号6471-78-9の4-アミノ-5-メトキシ-2-トルエンサルホニック酸は、GHS分類では corrosive(腐食性)と識別されます。EUのREAC...

6471-78-94-Amino-5-Methoxy-2-...
化合物よくある質問

甲基孕酮を取り扱う際の実験室安全事項は何ですか?

甲基孕酮の取り扱いは、PPE(個人保護具)の使用が必要な重要な安全事項を伴います。防塵マスク、ゴーグル、手袋を着用することが推奨されます。ドラフトチャンバーを使...

204063-33-22-[(Diphenylmethyl)a...

掲載誌

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
自己引用率: 10.3%
年間論文数: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

おすすめサプライヤー

免責事項
このページに表示される学術雑誌情報は、参考および研究目的のみを目的としています。当社は雑誌出版社とは提携しておらず、投稿の取り扱いも行っておりません。出版に関するお問い合わせは、各雑誌出版社に直接ご連絡ください。
表示されている情報に誤りがある場合は、support@chemtradehub.com までご連絡ください。迅速に確認し、対応いたします。