دورية أكاديمية
High-Concentration Alkane Output via In Situ Thermal-Assisted Photocatalytic Decarboxylation of Biomass-Derived Fatty Acid
العنوان: | High-Concentration Alkane Output via In Situ Thermal-Assisted Photocatalytic Decarboxylation of Biomass-Derived Fatty Acid |
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المؤلفون: | Chunlin Hao, Shukui Wu, Guibao Guo, Shengli An |
سنة النشر: | 2024 |
مصطلحات موضوعية: | Biophysics, Biochemistry, Microbiology, Molecular Biology, Physiology, Biotechnology, Immunology, Cancer, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, traditional far less, sup >– sup, sup >+ sup, presently challenging due, photogenerated electron consumption, concentration bioderived long, single output concentration, room temperature onto, assisted photocatalytic decarboxylation, photocatalytic decarboxylation reaction, maximum reaction temperature, incident light energy, 4 sub, 3 sub, >- alkane solvents, chain fatty acids, photocatalytic decarboxylation, fatty acids, >- alkane, n < |
الوصف: | Production of alkane fuels from fatty acids by photocatalytic decarboxylation is presently challenging due to low product output efficiency. Here, we report a high-efficiency photocatalytic decarboxylation route, achieving the transformation of high-concentration bioderived long-chain fatty acids to C1-shortened n -alkanes only by using the in situ heat from the photothermal conversion of Fe 3 O 4 . Through the use of high-boiling-point n -alkane solvents for getting the maximum reaction temperature, the single output concentration of C n –1 n -alkane was upgraded from a traditional far less than mmol/L level to the unprecedented mol/L level. We suggest that the heat enhances the strain of aimed C–COO – bond by forcing the standing C-chain down at room temperature onto the Fe 3 O 4 surface, leading photoinduced hole–electron pair easily to be close to and react with the energy-storing C–COO – bond. Meanwhile, the photogenerated electron consumption can shift from conventional PCET of the photo-Koble reaction into a stepwise pathway to form a more favorable carbanion (R – ) intermediate that reacting with H + into RH is highly accelerated with lifting the temperature. Our findings open a new way to upgrade the output efficiency of photocatalytic decarboxylation reaction by reusing the vast majority of incident light energy in a heat form. |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | unknown |
العلاقة: | https://figshare.com/articles/journal_contribution/High-Concentration_Alkane_Output_via_In_Situ_Thermal-Assisted_Photocatalytic_Decarboxylation_of_Biomass-Derived_Fatty_Acid/25158211Test |
DOI: | 10.1021/acssuschemeng.3c07864.s001 |
الإتاحة: | https://doi.org/10.1021/acssuschemeng.3c07864.s001Test https://figshare.com/articles/journal_contribution/High-Concentration_Alkane_Output_via_In_Situ_Thermal-Assisted_Photocatalytic_Decarboxylation_of_Biomass-Derived_Fatty_Acid/25158211Test |
حقوق: | CC BY-NC 4.0 |
رقم الانضمام: | edsbas.716D2FC3 |
قاعدة البيانات: | BASE |
DOI: | 10.1021/acssuschemeng.3c07864.s001 |
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