2025/08/06 更新

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写真a

ウランプリー ムハメド アシク
URAMPULLY MUHAMMED ASHIK
URAMPULLY MUHAMMED ASHIK
所属
先導物質化学研究所 先端素子材料部門 助教
職名
助教
連絡先
メールアドレス
プロフィール
私の研究は、バイオマスの化学品および合成ガス(シンガス)への変換、触媒によるバイオガス改質、および二酸化炭素(CO₂)回収技術に焦点を当てています。メタン改質やバイオマス由来チャーのCO₂ガス化のための高性能触媒の開発、CO₂選択性の高い吸着材の設計・合成に取り組んでいます。さらに、ナノ材料合成、水素製造、水処理・浄化技術にも関心があります。現在は、温室効果ガスを付加価値のある製品へと変換するための触媒および材料技術の統合的な開発を進めています。

研究分野

  • ナノテク・材料 / ナノ材料科学

  • ものづくり技術(機械・電気電子・化学工学) / 反応工学、プロセスシステム工学

  • ものづくり技術(機械・電気電子・化学工学) / 触媒プロセス、資源化学プロセス

  • ものづくり技術(機械・電気電子・化学工学) / 触媒プロセス、資源化学プロセス

経歴

  • 九州大学 先導物質化学研究所 助教 

    2025年7月 - 現在

  • 九州大学 先導物質化学研究所 Appointed Assistant Professor 

    2023年5月 - 2024年12月

  • 九州大学 先導物質化学研究所 学術研究員 

    2017年1月 - 2023年4月

  • University of Malaya Department of Chemical Engineering PhD Researcher (Research Assistant) 

    2012年9月 - 2016年10月

  • Central Electrochemical Research Institute Electrochemical Power Systems Division Graduate Research Assistant 

    2011年10月 - 2012年2月

  • M.E.S Ponnani College Department of Chemistry Lecturer 

    2010年6月 - 2011年2月

  • Indian Institute of Science Education and Research Computational and Theoretical Chemistry Graduate Research Assistant 

    2009年12月 - 2010年5月

▼全件表示

学歴

  • University of Malaya   Chemical Engineering   Doctorate

    2012年9月 - 2016年10月

  • Mahatma Gandhi University   International and Inter University Centre for Nanoscience and Nanotechnology   Master of Philosophy

    2011年3月 - 2012年6月

  • Mahatma Gandhi University   School of Chemical Sciences   Master of Science

    2008年7月 - 2010年6月

研究テーマ・研究キーワード

  • 研究テーマ: Biomass to chemicals

    研究キーワード: Biomass to chemicals

    研究期間: 2025年

  • 研究テーマ: Catalysis

    研究キーワード: Catalysis

    研究期間: 2025年

  • 研究テーマ: CO2 adsorption materials

    研究キーワード: CO2 adsorption materials

    研究期間: 2025年

  • 研究テーマ: Gasification

    研究キーワード: Gasification

    研究期間: 2025年

  • 研究テーマ: hydrogen energy

    研究キーワード: hydrogen energy

    研究期間: 2025年

  • 研究テーマ: Nanocynthesis

    研究キーワード: Nanocynthesis

    研究期間: 2025年

  • 研究テーマ: Syn-gas from methane dry reforming

    研究キーワード: Syn-gas from methane dry reforming

    研究期間: 2025年

受賞

  • Outstanding contribution in reviewing

    2017年   International Journal of Hydrogen Energy  

  • Best paper presenter award

    2016年   International Conference on Green and Sustainable Technology, Dubai  

  • Best paper presenter award

    2016年   International Conference On Green And Sustainable Technology, Malaysia  

論文

  • Promotion of Cross-Linking and Resulting Suppression of Tar Evolution in Potassium-Catalyzed Pyrolysis of Woody Biomass

    Sun H., Ashik U.P.M., Asano S., Kudo S., Takeyama Y., Hayashi J.I.

    Energy and Fuels   39 ( 1 )   479 - 490   2025年1月   ISSN:08870624

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    出版者・発行元:Energy and Fuels  

    Acid-washed woody biomass (cedar) was impregnated with K<inf>2</inf>CO<inf>3</inf> and then pyrolyzed at 550 °C in a fixed bed reactor, in which extra-particle pyrolysis of volatile matter was well suppressed. The tar yield decreased from 0.42 to 0.034 kg/kg-daf with increasing K loading (m<inf>K,0</inf>) within the range of 0-5.0 mol K/kg-daf. The K-catalyzed condensation by dehydration, dehydrogenation, and dealkylation reactions formed H<inf>2</inf>O, H<inf>2</inf>, and gaseous hydrocarbons (GHCs), respectively, producing intermonomer-unit cross-links (MUCs) and thereby decreasing the yield of tar as monomers and oligomers. According to the conversion of K<inf>2</inf>CO<inf>3</inf> (34-57%), three catalytic cycles were estimated with the conversion/regeneration of K<inf>2</inf>CO<inf>3</inf>, KOH, and alkoxides/phenoxides, formation of inter-MUCs and that of the above-mentioned gases. The relationship between the amount of inter-MUCs formed during the pyrolysis (assumed to be 30% of that of H<inf>2</inf>O, H<inf>2</inf>, and GHCs on a molar basis) and reduction in the tar yield was considered by applying the Bethe lattice model, which is often employed for analyzing degradation and repolymerization of polymer, coal, and biomass. The model described the above relationship semiquantitatively. The efficiency of the K loading for the tar reduction, represented by the derivative of the tar yield (Y<inf>tar</inf>) with respect to m<inf>K,0</inf>, i.e., dY<inf>tar</inf>/dm<inf>K,0</inf>, was decreased by a factor of about 340 while m<inf>K,0</inf> increased from 0 to 5.0 mol K/kg daf. Such a large factor was explained by decreases in the two derivatives, dY<inf>tar</inf>/dY<inf>inter-MUC</inf> (Y<inf>inter-MUC</inf>; the amount of inter-MUCs) and dY<inf>inter-MUC</inf>/dm<inf>K,0</inf>, quantitatively. The decrease in the dY<inf>inter-MUC</inf>/dm<inf>K,0</inf> (factor ≈ 30) was mainly due to the depletion of functional groups that underwent condensation reactions while that in the dY<inf>tar</inf>/dY<inf>inter-MUC</inf> (factor ≈ 11.6) arose from the nature of network polymer such as approximation by the Bethe lattice.

    DOI: 10.1021/acs.energyfuels.4c05005

    Scopus

  • Staged Conversion of Potassium-Loaded Biomass into Syngas by Continuous Pyrolysis and Low-Temperature Reforming/Gasification with CO2 and O2

    Sun H., Ashik U.P.M., Hu G., Kudo S., Asano S., Hayashi J.I.

    Energy and Fuels   39 ( 1 )   465 - 478   2025年1月   ISSN:08870624

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    出版者・発行元:Energy and Fuels  

    CO<inf>2</inf>-O<inf>2</inf>-blown gasification of dry biomass can potentially produce syngas with maximized yield of CO, in other words, the rate of carbon recuperation. Among various types of gasification, staged conversion consisting of pyrolysis, volatile reforming, and char gasification is expected to give the highest cold gas efficiency (i.e., recuperation rate of biomass chemical energy) if endothermic pyrolysis is driven by the heat of syngas from the reforming/gasification. Catalytic char gasification, if operated at a temperature well below 800 °C, may enable the avoidance of ash-related troubles such as clinker formation/accumulation in the gasifier while achieving fast and complete char conversion to syngas. We simulated numerically the above staged conversion of woody biomass with potassium (K) and CO<inf>2</inf>-O<inf>2</inf> as the catalyst and gasifying agent, respectively, and then experimentally by applying screw-conveyor pyrolysis at 550 °C and downdraft gasification/reforming at 730 °C. It was revealed that the biomass with 1.0 mol-K/kg-dry loading was converted to gas completely by applying CO<inf>2</inf>/C and O<inf>2</inf>/C molar ratios of ≥0.42 and ≈0.30, respectively. The CO yield and apparent cold gas efficiency were both 94% on biomass carbon and LHV bases, respectively. The concentrations of residual heavy tar (molecular mass >200) and light tar (<200) were 0.1-0.7 and 0.7-8.5 mg/Nm<sup>3</sup>-dry, respectively, over the range of CO<inf>2</inf>/C ratios (0.42-0.72) investigated. The carbon conversion to gas and tar concentrations were sensitive to the K loading, gasification/reforming temperature, CO<inf>2</inf>/C ratio, and O<inf>2</inf>/C ratio.

    DOI: 10.1021/acs.energyfuels.4c04728

    Scopus

  • Effect of Initial Potassium Catalyst Concentration on Its Activity and Fate in CO2 Gasification of Lignite Char

    Sun H., Ashik U.P.M., Asano S., Kudo S., Takeyama Y., Hayashi J.I.

    Energy and Fuels   2025年   ISSN:08870624

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    出版者・発行元:Energy and Fuels  

    K-catalyzed gasification of char and carbon has been studied for more than 40 years while many different types of relationships between specific rate of gasification (r<inf>sp</inf> = (Formula presented), X; char conversion) and K concentration in gasifying char/carbon (C<inf>K</inf>) have been reported. This work explored the mechanism causing such diversity in the r<inf>sp</inf>-C<inf>K</inf> profile. An ash-free lignite was impregnated with K<inf>2</inf>CO<inf>3</inf>, devolatilized, and then gasified with CO<inf>2</inf> at 800 °C and C<inf>K</inf> at the start of gasification (C<inf>K,0</inf>) of 0.15-2.66 mol-K/kg-daf-char. C<inf>K</inf> was accurately determined by measuring the K volatilization rate as a function of X. For C<inf>K,0</inf> = 0.15, r<inf>sp</inf> increased linearly with C<inf>K</inf> while the K catalyst activity (k<inf>c</inf>′ = r<inf>sp</inf>/C<inf>K</inf>) remained unchanged at 0.013 min<sup>-1</sup> mol-K/kg-daf-char<sup>-1</sup>. The K species underwent transformation to much more active catalyst (k<inf>c</inf>′ ≈ 0.130 min<sup>-1</sup> mol-K/kg-daf-char<sup>-1</sup>) for C<inf>K,0</inf> = 0.64-2.66, where the r<inf>sp</inf>-C<inf>K</inf> profile was independent of C<inf>K,0</inf>, and r<inf>sp</inf> reached an upper limit due to saturation of gasifying char matrix with the catalyst. The catalyst transformation also occurred for C<inf>K,0</inf> = 0.28-0.39 while k<inf>c</inf>′ of the transformed catalyst was steady at 0.03-0.08 depending on C<inf>K,0</inf>. Thus, the variety of the r<inf>sp</inf>-C<inf>K</inf> profile arose from that in C<inf>K,0</inf>. Higher C<inf>K,0</inf> led to greater dX/dt and then dC<inf>K</inf>/dt under a steady supply of oxygen (as CO<inf>2</inf>) that anchored K on the char surface, allowing atomic-level dispersed C-O-K and/or K<inf>2</inf>CO<inf>3</inf> to transform into clusters consisting of K<inf>x</inf>O<inf>y</inf>(CO<inf>2</inf>)<inf>z</inf> (y/x > 0.5, z/x ≈ 0.16). The most active cluster was formed even during the period of devolatilization for C<inf>K,0</inf> > 1.69. Increasing C<inf>K,0</inf> from 0.15 to 2.66 (by a factor of 18) resulted in shortening of the time required for X = 0.50 and 0.99 by factors as large as 1/200 and 1/100, respectively, due to the above-mentioned C<inf>K,0</inf> effect on the r<inf>sp</inf>-C<inf>K</inf> relationship.

    DOI: 10.1021/acs.energyfuels.4c05914

    Scopus

  • Comparative Analysis of Commercial and Synthesized Molybdenum Disulfide for Progesterone Removal in Water Treatment

    Bessai S., Falyouna O., Mandai T., Ashik U.P.M., Eljamal O.

    International Exchange and Innovation Conference on Engineering and Sciences   10   1071 - 1077   2024年

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    出版者・発行元:International Exchange and Innovation Conference on Engineering and Sciences  

    Water contamination by Endocrine Disrupting Chemicals (EDCs), such as progesterone, is a significant environmental concern. This study uniquely investigates the efficacy of synthesized molybdenum disulfide (S-MoS<inf>2</inf>) compared to commercial molybdenum disulfide (C-MoS<inf>2</inf>) for progesterone removal from water. Batch experiments evaluated the removal efficiency of both types under various dosages and pH conditions. Preliminary results indicate that S-MoS<inf>2</inf>achieves 12.8% higher removal efficiency than C-MoS<inf>2</inf>. This results of the enhanced properties of S-MoS<inf>2</inf> attributed to its synthesis. Dosage experiments showed a 10.7% improvement at an optimal dosage of 20 mg/L (87.8% vs. 79.3%). Additionally, pH variation experiments revealed the highest removal efficiency at pH 7, with a 14.8% improvement (89.3% vs. 77.8%). These findings highlight the superior performance of S-MoS<inf>2</inf>, demonstrating its potential for effective progesterone removal in water treatment applications. This research is the first of its kind to compare synthesized and commercial MoS<inf>2</inf> for this purpose, marking a significant advancement in the field of water treatment.

    DOI: 10.5109/7323391

    Scopus

  • Control of Reactivity of Formed Coke from Torrefied Biomass by Its Washing with Torrefaction-derived Acidic Water

    Wibawa A., Ashik U.P.M., Kudo S., Asano S., Dohi Y., Yamamoto T., Hayashi J.I.

    ISIJ International   63 ( 9 )   1545 - 1556   2023年   ISSN:09151559

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    出版者・発行元:ISIJ International  

    Torrefaction, pulverization, hot briquetting, and carbonization in sequence successfully produce highstrength coke from woody biomass. This method was further improved by introducing washing of torrefied biomass with acidic water from torrefaction before briquetting. The primary purpose of the washing was to remove alkali, and alkaline-earth metallic species of which catalyses were responsible for high reactivity of the coke. The acidic water (AW) from 275°C torrefaction of Japanese cedar contained 12, 0.9, and 39.4 mass% of acetic and formic acids, and the other organic compounds, respectively. A simulated AW (SAW) was prepared with the same composition as that of AW. SAW with pH of 1.95 removed 96-97% of K, Mg, and Ca and 48% of Na from the torrefied cedar. These removal rates were higher than those by washing with an aqueous solution of acetic acid, hydrogen chloride, or oxalic acid with pH of 2.35, 1.05, or 0.77, respectively. Organic compounds dissolved in SAW helped water and acids penetrate the matrix of the cedar. The washing with SAW increased the tensile strength of coke from 16 to 21 MPa by promoting volumetric shrinkage of the briquette during the carbonization and then particle bonding and coalescence. More importantly, the washing greatly reduced coke reactivity. The times required for gasifying 50% and 99% of coke with 50 kPa CO<inf>2</inf> at 900°C, t<inf>0.50</inf> and t<inf>0.99</inf>, respectively, were extended by factors of 24 and 46, respectively. It was thus demonstrated that the coke reactivity was controllable over such a wide range.

    DOI: 10.2355/isijinternational.ISIJINT-2022-537

    Scopus

  • Kinetics and Mechanisms of Selected Reactions over Hydroxyapatite‐Based Catalysts

    U.P.M. Ashik, Nurulhuda Halim, Shusaku Asano, Shinji Kudo, Jun‐ichiro Hayashi

    Design and Applications of Hydroxyapatite‐Based Catalysts   163 - 199   2022年9月   ISBN:9783527348497, 9783527830190

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    記述言語:英語   出版者・発行元:Wiley  

    DOI: 10.1002/9783527830190.ch5

  • High-Strength Formed Coke from Torrefied Biomass and Its Blend with Noncaking Coal

    Wibawa A., Ashik U.P.M., Kudo S., Asano S., Gao X., Hayashi J.I.

    Energy and Fuels   36 ( 16 )   9121 - 9132   2022年8月   ISSN:08870624

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    出版者・発行元:Energy and Fuels  

    In continuation of our previous study on production of high-strength metallurgical coke from torrefied softwood (cedar), we studied coke production from a mixture of torrefied cedar (TC) and noncaking coal by pulverization to sizes <100 μm, mixing, binderless hot briquetting, and carbonization. These sequential processes produced coke with a tensile strength of 5-17 MPa, which was equivalent to or greater than that of conventional coke (5-6 MPa), from TC-coal mixtures over the entire ranges of TC mass fraction in briquette of 0-100%, torrefaction temperature of 250-300 °C, and choice of coal (sub-bituminous or medium-volatile bituminous coal). The mixing of TC and coal hindered densification of coke due to hindrance of shrinkage of more-shrinkable TC-derived particles during the carbonization under many of the conditions. Nevertheless, positive synergy occurred in the coke strength at TC mass fractions of over 50%, where coal-derived particles were dispersed in the matrix of TC-derived particles, bonded to them during the carbonization, and behaved as a reinforcement of the matrix. The bonding between TC-derived and coal-derived primary particles was revealed by scanning electron microscopy. Copulverization of mixed TC and coal to sizes <40 μm before the briquetting gave cokes having strengths as high as 23-28 MPa. The fine pulverization increased the frequencies of mutual bonding of TC-derived particles and coal-derived particles and bonding between TC-derived and coal-derived particles per coke volume. The strength of coke from the TC-coal mixture generally followed volume-based additivity of strengths of cokes from TC and coal. This was realized by mixing primary particles of TC and coal within ≈10 μm scale or even smaller.

    DOI: 10.1021/acs.energyfuels.2c01722

    Scopus

  • Promotion of ciprofloxacin adsorption from contaminated solutions by oxalate modified nanoscale zerovalent iron particles

    Falyouna O., Faizul Idham M., Maamoun I., Bensaida K., Ashik U.P.M., Sugihara Y., Eljamal O.

    Journal of Molecular Liquids   359   2022年8月   ISSN:01677322

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    出版者・発行元:Journal of Molecular Liquids  

    Water contamination by ciprofloxacin (CIP) is a global and emerging issue because it increases the risk of infection by antimicrobial resistant bacteria. CIP removal from water by iron nanoparticles (Fe<sup>0</sup>) with the presence of oxalate hasn't been reported yet. The present study demonstrated that the addition of oxalate to Fe<sup>0</sup> nanoparticles improved the removal of 100 mg L<sup>−1</sup> of CIP from 45.04% to 95.74% under the following optimum conditions: [Fe<sup>0</sup>] = 0.3 g L<sup>−1</sup>, [oxalate] = 0.3 mM, initial pH = 7, and temperature = 25 ℃. Furthermore, the experimental results illustrated that high concentrations of dissolved oxygen in the aqueous solution greatly decreased the removal efficiency of CIP by (Fe<sup>0</sup>/oxalate) system from 97.69% (N<inf>2</inf> atmosphere) to 67.47%. Similarly, the performance of (Fe<sup>0</sup>/oxalate) system declined from 95.43% to 85.23% because of increasing the ionic strength of the solution from 0 to 100 mM. In contrast, the influence of humic acid (0 – 40 mg L<sup>−1</sup>) on the removal of CIP by (Fe<sup>0</sup>/oxalate) system was neglectable. Also, the negative impact of coexisting ions on the competence of (Fe<sup>0</sup>/oxalate) system was in the following order: Mg<sup>2+</sup> > NO<inf>3</inf><sup>–</sup> > SO₄<sup>2-</sup> > Ca<sup>2+</sup> > CO<inf>3</inf><sup>2–</sup> > K<sup>+</sup>. In addition, the desorption experiments and the results of SEM-EDS, XRD, and FTIR revealed that physisorption and chemisorption were responsible for CIP removal by (Fe<sup>0</sup>/oxalate) system as the addition of 0.3 mM of oxalate boosted the surface complexation between Fe<sup>0</sup> nanoparticles and the carboxylic, ketone, and piperazinyl groups in CIP. These results were supported by the outcomes of kinetics, isotherm, and thermodynamic analysis. Moreover, oxalate addition significantly reduced the treatment cost of 1 L of 100 mg L<sup>−1</sup> of CIP and the generated sludge by approximately 55.68% and 57%, respectively. Finally, this study proved that (Fe<sup>0</sup>/oxalate) system is inexpensive, practical, and more efficient than most of the reported Fe<sup>0</sup>-based systems with a maximum adsorption capacity of 294.66 mg g<sup>−1</sup>.

    DOI: 10.1016/j.molliq.2022.119323

    Scopus

  • Synthesis of hybrid magnesium hydroxide/magnesium oxide nanorods [Mg(OH)2/MgO] for prompt and efficient adsorption of ciprofloxacin from aqueous solutions

    Falyouna O., Bensaida K., Maamoun I., Ashik U.P.M., Tahara A., Tanaka K., Aoyagi N., Sugihara Y., Eljamal O.

    Journal of Cleaner Production   342   2022年3月   ISSN:09596526

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    出版者・発行元:Journal of Cleaner Production  

    The antibiotic ciprofloxacin (CIP) is recognized as a contaminant of emerging concern because its persistent occurrence in water accelerates the growth of deadly antimicrobial resistance genes (AMRs). For the first time, the conventional precipitation technique was thermally modified to produce hybrid magnesium hydroxide/magnesium oxide nanorods [Mg(OH)<inf>2</inf>/MgO] for efficient and rapid adsorption of CIP from water. The successful synthesis of Mg(OH)<inf>2</inf>/MgO was confirmed by the outcomes of TEM, EDS, XRD, and FTIR analysis. Mg(OH)<inf>2</inf>/MgO exhibited an extraordinary capability to adsorb CIP from water regardless of CIP initial concentration where more than 97% of 200 mg L<sup>−1</sup> of CIP was promptly eliminated within 30 min by 0.1 g L<sup>−1</sup> of Mg(OH)<inf>2</inf>/MgO under neutral pH and room temperature. These results clearly state that Mg(OH)<inf>2</inf>/MgO is at least 2-fold efficient and 20-fold faster in removing CIP than the reported nanomaterials with exceptional adsorption capacity higher than 1789 mg g<sup>−1</sup>. FTIR analysis for the spent Mg(OH)<inf>2</inf>/MgO revealed that bridging complexation with carboxylic group and electrostatic attraction with the positive amine group are the responsible mechanisms for CIP adsorption by Mg(OH)<inf>2</inf>/MgO. Moreover, simulated CIP-contaminated river water was efficiently treated by Mg(OH)<inf>2</inf>/MgO which proves the promising performance of Mg(OH)<inf>2</inf>/MgO in field scale applications.

    DOI: 10.1016/j.jclepro.2022.130949

    Scopus

  • Catalytic deep eutectic solvent for levoglucosenone production by pyrolysis of cellulose

    Saragai S., Kudo S., Sperry J., Ashik U.P.M., Asano S., Hayashi J.i.

    Bioresource Technology   344   2022年1月   ISSN:09608524

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    出版者・発行元:Bioresource Technology  

    This work presents the selective production of the versatile bio-based platform levoglucosenone (LGO) using deep eutectic solvents (DESs) as catalysts during cellulose pyrolysis. Among 18 types of DESs examined, those containing p-toluenesulfonic acid as a hydrogen bond donor possessed the requisite thermal stability for use in the pyrolysis of cellulose. When those DESs were combined with cellulose, the pyrolysis temperature could be reduced which led to greater selectivity for LGO, the highest yield being 41.5% on a carbon basis. Because of their thermal stability, the DESs could be recovered from the pyrolysis residue and reused. The DESs recovery reached 97.9% in the pyrolysis at a low temperature with the LGO yield of 14.0%. Thus, DES-assisted cellulose pyrolysis is a promising methodology for LGO production.

    DOI: 10.1016/j.biortech.2021.126323

    Scopus

  • Preparation of Formed Coke from Biomass by Sequence of Torrefaction, Binderless Hot Briquetting and Carbonization

    Wibawa A., Ashik U.P.M., Kudo S., Asano S., Dohi Y., Yamamoto T., Kimura Y., Xiangpeng G.A.O., Hayashi J.I.

    ISIJ International   62 ( 8 )   1629 - 1638   2022年   ISSN:09151559

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    出版者・発行元:ISIJ International  

    This paper proposes a method of preparing high-strength formed coke from woody biomass without binder. Chipped and pre-dried Japanese cedar was heat-treated in an inert atmosphere (i.e., torrefied) at 225–325°C (Tt), pulverized to sizes in three different ranges, molded into briquettes (in the form of thick disk with diameter/thickness ≈ 2.5) at temperature up to 200°C by applying mechanical pressure of 128 MPa. The torrefied/briquetted cedar (TBC) was then converted into coke by heating to 1 000°C in an inert atmosphere at normal pressure. This process sequence enabled to prepare coke having indirect tensile strength (St) of 8–32 MPa, which was much higher than that without torrefaction, below 5 MPa. The torrefaction greatly improved pulverizability of the cedar, which was further promoted by increasing Tt. St of TBC and that of coke both increased as the particle sizes of TBC decreased, but this explained only a minor part of significant effect of Tt on St of the coke. St was maximized at Tt = 275°C regardless of the degree of pulverization. The Tt effects on physicochemical properties of TBC and coke were investigated in detail. The difference in St of coke by Tt was mainly due to that in the increment of St along the carbonization at 500–1 000°C. Fracture surfaces of the coke had particular morphologies that had been inherited from the original honeycomb structure of the cedar.

    DOI: 10.2355/isijinternational.ISIJINT-2022-013

    Scopus

  • Impact of reactor materials on methane decomposition for hydrogen production

    Hazzim F. Abbas, U. P.M. Ashik, Salam A. Mohammed, Wan Mohd Ashri Wan Daud

    Chemical Engineering Research and Design   174   127 - 136   2021年10月   ISSN:0263-8762

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    掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.cherd.2021.08.005

    Scopus

  • Review on the catalytic tri-reforming of methane - Part II: Catalyst development

    Xuan Huynh Pham, U. P.M. Ashik, Jun Ichiro Hayashi, Alejandro Pérez Alonso, Daniel Pla, Montserrat Gómez, Doan Pham Minh

    Applied Catalysis A: General   623   2021年8月   ISSN:0926-860X

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    掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.apcata.2021.118286

    Scopus

  • Microwave-assisted dry reforming of methane for syngas production: a review

    T. T., Phuong Pham, Kyoung S. Ro, Lyufei Chen, Devinder Mahajan, Tan Ji Siang, U. P. M. Ashik, Jun-ichiro Hayashi, Doan Pham Minh, Dai-Viet N. Vo

    Environmental Chemistry Letters   2020年7月   ISSN:1610-3653

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Springer Science and Business Media {LLC}  

    DOI: 10.1007/s10311-020-01055-0

  • Selective Hydrodeoxygenation of γ -Valerolactone over Silica-supported Rh-based Bimetallic Catalysts

    Xin Huang, Shinji Kudo, U. P.M. Ashik, Hisahiro Einaga, Jun Ichiro Hayashi

    Energy and Fuels   34 ( 6 )   7190 - 7197   2020年6月   ISSN:0887-0624 eISSN:1520-5029

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    掲載種別:研究論文(学術雑誌)  

    DOI: 10.1021/acs.energyfuels.0c01290

    Scopus

  • Methane decomposition with a minimal catalyst: An optimization study with response surface methodology over Ni/SiO2 nanocatalyst 査読

    U.P.M. Ashik, Hazzim F. Abbas, Faisal Abnisa, Shinji Kudo, Jun-ichiro Hayashi, W.M.A. Wan Daud

    International Journal of Hydrogen Energy   45 ( 28 )   14383 - 14395   2020年5月

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    担当区分:筆頭著者, 責任著者   掲載種別:研究論文(学術雑誌)   出版者・発行元:Elsevier {BV}  

    DOI: 10.1016/j.ijhydene.2020.03.164

  • The Distinctive Effects of Glucose-Derived Carbon on the Performance of Ni-Based Catalysts in Methane Dry Reforming 査読

    U. P. M. Ashik, Shusaku Asano, Shinji Kudo, Doan Pham Minh, Srinivas Appari, Einaga Hisahiro, Jun-ichiro Hayashi

    CATALYSTS   10 ( 1 )   2020年1月   eISSN:2073-4344

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.3390/catal10010021

    Web of Science

  • Production of High-strength Cokes from Non- and Slightly Caking Coals. Part II: Application of Sequence of Fine Pulverization of Coal, Briquetting and Carbonization to Single Coals and Binary Blends 査読

    Muhammed Ashik Urampully

    ISIJ International   2019年8月   ISSN:0915-1559

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.2355/isijinternational.isijint-2018-847

  • Quantitative Description of Catalysis of Inherent Metallic Species in Lignite Char during CO2 Gasification 査読

    Muhammed Ashik Urampully

    Energy & Fuels   2019年7月   ISSN:0887-0624

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1021/acs.energyfuels.9b00465

  • Effect of SiO2 on loss of catalysis of inherent metallic species in CO2 gasification of coke from lignite 査読

    Cheolyong Choi, U.P.M. Ashik, Shinji Kudo, Kazuya Uebo, Koyo Norinaga, Jun-ichiro Hayashi

    Carbon Resources Conversion   2 ( 1 )   13   2019年4月

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    掲載種別:研究論文(学術雑誌)   出版者・発行元:Elsevier {BV}  

    DOI: 10.1016/j.crcon.2018.09.002

  • The effect of ZSM-5 framework in non-oxidative coupling of methane 査読

    2018年10月

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  • CO2 Gasification of Sugar Cane Bagasse: Quantitative Understanding of Kinetics and Catalytic Roles of Inherent Metallic Species 査読

    Zayda Faizah Zahara, Shinji Kudo, Daniyanto, U. P.M. Ashik, Koyo Norinaga, Arief Budiman, Jun-Ichiro Hayashi

    Energy and Fuels   32 ( 4 )   4255 - 4268   2018年4月   ISSN:1520-5029

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:American Chemical Society  

    DOI: 10.1021/acs.energyfuels.7b03147

    Scopus

  • Nanomaterials as Catalysts 査読

    Muhammed Ashik Urampully

    Applications of Nanomaterials   2018年   ISBN:9780081019719

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  • An Overview of Metal Oxide Nanostructures 査読

    Muhammed Ashik Urampully

    Synthesis of Inorganic Nanomaterials   2018年   ISBN:9780081019757

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  • Governance of the porosity and of the methane decomposition activity sustainability of NiO/SiO 2 nanocatalysts by changing the synthesis parameters in the modified Stöber method 査読

    U.P.M. Ashik, W.M.A, Wan Daud, Jun-Ichiro Hayashi

    Comptes Rendus Chimie   20 ( 9-10 )   896 - 909   2017年9月   ISSN:1631-0748 eISSN:1878-1543

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.crci.2017.06.007

    Web of Science

  • A review on methane transformation to hydrogen and nanocarbon: Relevance of catalyst characteristics and experimental parameters on yield 査読

    U. P. M. Ashik, W. M. A. Wan Daud, Jun-ichiro Hayashi

    RENEWABLE & SUSTAINABLE ENERGY REVIEWS   76   743 - 767   2017年9月   ISSN:1364-0321

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    記述言語:英語  

    DOI: 10.1016/j.rser.2017.03.088

    Web of Science

  • Methane decomposition kinetics and reaction rate over Ni/SiO 2 nanocatalyst produced through co-precipitation cum modified Stöber method 査読

    U.P.M. Ashik, W.M.A, Wan Daud, Hazzim F. Abbas

    International Journal of Hydrogen Energy   42 ( 2 )   938 - 952   2017年1月   ISSN:0360-3199 eISSN:1879-3487

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.ijhydene.2016.09.025

    Web of Science

  • Stabilization of Ni, Fe, and Co nanoparticles through modified Stöber method to obtain excellent catalytic performance: Preparation, characterization, and catalytic activity for methane decomposition 査読

    U.P.M. Ashik, W.M.A, Wan Daud

    Journal of the Taiwan Institute of Chemical Engineers   61   247 - 260   2016年4月   ISSN:1876-1070 eISSN:1876-1089

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.jtice.2015.12.019

    Web of Science

    その他リンク: http://orcid.org/0000-0001-7259-0482

  • STABILITY ENHANCEMENT OF NANO-NiO CATALYST WITH SiO2 SUPPORT TO GET IMPROVED HYDROGEN YIELD FROM METHANE DECOMPOSITION 査読

    Muhammed Ashik Urampully

    MATTER: International Journal of Science and Technology   2015年5月   ISSN:2454-5880

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    掲載種別:研究論文(学術雑誌)  

    DOI: 10.20319/mijst.2016.21.4252

  • Production of greenhouse gas free hydrogen by thermocatalytic decomposition of methane – A review 査読

    Ashik U. P. M, Wan Daud, W. M. A, Abbas Hazzim F

    Renewable and Sustainable Energy Reviews   44 ( 0 )   221 - 256   2015年4月   ISSN:1364-0321

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    記述言語:英語  

    DOI: 10.1016/j.rser.2014.12.025

    Web of Science

  • Probing the differential methane decomposition behaviors of n-Ni/SiO2, n-Fe/SiO2 and n-Co/SiO2 catalysts prepared by co-precipitation cum modified Stöber method 査読

    U. P. M. Ashik, W. M. A. Wan Daud

    RSC Advances   5 ( 82 )   67227 - 67241   2015年   ISSN:2046-2069

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1039/c5ra10997c

    Web of Science

    その他リンク: http://orcid.org/0000-0001-7259-0482

  • Nanonickel catalyst reinforced with silicate for methane decomposition to produce hydrogen and nanocarbon: synthesis by co-precipitation cum modified Stöber method 査読

    RSC Advances

    RSC Advances   5 ( 58 )   46735 - 46748   2015年   ISSN:2046-2069

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1039/c5ra07098h

    Web of Science

    その他リンク: http://orcid.org/0000-0001-7259-0482

  • Nucleic Acid G-quartets: Insights into Diverse Patterns and Optical Properties 査読

    A. K. Jissy, U. P. M. Ashik, Ayan Datta

    JOURNAL OF PHYSICAL CHEMISTRY C   115 ( 25 )   12530 - 12546   2011年6月   ISSN:1932-7447

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1021/jp202401b

    Web of Science

    その他リンク: http://orcid.org/0000-0001-7259-0482

▼全件表示

講演・口頭発表等

  • Co-production of hydrogen and nano-carbon from methane 国際会議

    Ashik, U. P. M, Daud, W. M. A

    World Sustainable Energy Days – 2016  2016年2月 

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    記述言語:英語   会議種別:口頭発表(一般)  

  • Combined effects of operating variables and crystallinity of cellulose on its pyrolytic behavior 国際会議

    ウランプリー, ムハメド アシク

    APCChE 2019  2019年9月 

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    記述言語:英語   会議種別:ポスター発表  

  • Production of GHG free hydrogen from methane: significance of porosity of n-NiO/SiO2 nanocatalysts 国際会議

    Ashik, U. P. M, Daud, W. M. A

    16th International Conference on Green and Sustainable Technology (GSUS)  2016年5月 

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    記述言語:英語   会議種別:口頭発表(一般)  

  • Production of hydrogen and nanocarbon from methane over nNiO/SiO2 catalyst prepared by Co-precipitation cum modified Stöber method 国際会議

    Ashik, U. P. M, Daud, W. M. A

    14th International Conference on Green and Sustainable Technology (GSUS)  2016年2月 

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    記述言語:英語   会議種別:口頭発表(一般)  

  • Two-step Rapid Conversion of Cellulose to Glucose via Anhydrosugar 国際会議

    Ni’mah Ayu Lestari, Ashik.U.P.M, Shinji Kudo, Shusaku Asano, Jun-ichiro Hayashi

    International Conference of the Indonesian Chemical Society  2019年8月 

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    記述言語:英語   会議種別:口頭発表(一般)  

  • The effect of ZSM-5 framework in non-oxidative coupling of methane 国際会議

    Phatchada Santawaja, Ashik U.P.M, Shinji Kudo, Jun-ichiro Hayashi

    International Exchange and Innovation Conference on Engineering & Sciences  2018年10月 

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    記述言語:英語  

▼全件表示

学術貢献活動

  • Student spirit as a driving force to the nation's development

    役割:企画立案・運営等, パネル司会・セッションチェア等

    King Abdulaziz University  2021年2月

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    種別:大会・シンポジウム等 

  • Writing a Research Proposal: Tips for Students and Researchers

    役割:企画立案・運営等, パネル司会・セッションチェア等

    St. Stephen's College, Kerala, India  2020年9月

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    種別:大会・シンポジウム等 

  • Pros and cons of Migration: A Researcher's Perspective

    役割:企画立案・運営等, パネル司会・セッションチェア等

    Providence Women's College, Kerala, India  2020年9月

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    種別:大会・シンポジウム等 

共同研究・競争的資金等の研究課題

  • A novel core@shell structured dual faceted MOF-based sorbent for mega scale CO2 capture

    研究課題/領域番号:20K15077  2020年 - 2021年

    日本学術振興会  科学研究費助成事業  若手研究

    Urampully Muhammed・Ashik

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    担当区分:研究代表者  資金種別:科研費

    The research aim is to synthesis a novel polymer coated MOF sorbent to be used for CO2 capture applications. The internal and external active sites of sorbent material could help extensive CO2 sorption. Besides, the coating could improve the stability of MOF during sorption and regeneration cycle.

    CiNii Research

社会貢献活動

  • ആല്‍പ്സിന്‍റെ മടിത്തട്ടില്‍ (Alpsinte Madithattil) - Travel report

    役割:報告書執筆

    Varthamanam Daily, Qatar  Travel  2016年7月

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    種別:新聞・雑誌

    添付ファイル: Varthamanam Weekend Special Edition-28-07-2016-17-17_1.pdf

  • Inaugural Lecture by Prof. Wan Mohd Ashri Wan Daud

    役割:コメンテーター

    University of Malaya  Inaugural Lecture  2015年7月

  • Rasathanthra 2014

    役割:企画, 運営参加・支援

    Indian Association for Hydrogen Energy and Advanced Materials  Rasathanthra 2014  2014年9月

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    種別:セミナー・ワークショップ

    添付ファイル: Rasathanthra 20142108141549.pdf

  • Chem-Incipitia 2010

    役割:司会, 助言・指導, 企画, 運営参加・支援

    MES Ponnani College  MES Ponnani Mega Expo  2010年12月