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Search results for: Lotanna Ezeonu
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text-center" style="font-size:1.6rem;">Search results for: Lotanna Ezeonu</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4</span> Acetic Acid Adsorption and Decomposition on Pt(111): Comparisons to Ni(111)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Lotanna%20Ezeonu">Lotanna Ezeonu</a>, <a href="https://publications.waset.org/abstracts/search?q=Jason%20P.%20Robbins"> Jason P. Robbins</a>, <a href="https://publications.waset.org/abstracts/search?q=Ziyu%20Tang"> Ziyu Tang</a>, <a href="https://publications.waset.org/abstracts/search?q=Xiaofang%20Yang"> Xiaofang Yang</a>, <a href="https://publications.waset.org/abstracts/search?q=Bruce%20E.%20Koel"> Bruce E. Koel</a>, <a href="https://publications.waset.org/abstracts/search?q=Simon%20G.%20Podkolzin"> Simon G. Podkolzin</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The interaction of organic molecules with metal surfaces is of interest in numerous technological applications, such as catalysis, bone replacement, and biosensors. Acetic acid is one of the main products of bio-oils produced from the pyrolysis of hemicellulosic feedstocks. However, their high oxygen content makes them unsuitable for use as fuels. Hydrodeoxygenation is a proven technique for catalytic deoxygenation of bio-oils. An understanding of the energetics and control of the bond-breaking sequences of biomass-derived oxygenates on metal surfaces will enable a guided optimization of existing catalysts and the development of more active/selective processes for biomass transformations to fuels. Such investigations have been carried out with the aid of ultrahigh vacuum and its concomitant techniques. The high catalytic activity of platinum in biomass-derived oxygenate transformations has sparked a lot of interest. We herein exploit infrared reflection absorption spectroscopy(IRAS), temperature-programmed desorption(TPD), and density functional theory(DFT) to study the adsorption and decomposition of acetic acid on a Pt(111) surface, which was then compared with Ni(111), a model non-noble metal. We found that acetic acid adsorbs molecularly on the Pt(111) surface, interacting through the lone pair of electrons of one oxygen atomat 90 K. At 140 K, the molecular form is still predominant, with some dissociative adsorption (in the form of acetate and hydrogen). Annealing to 193 K led to complete dehydrogenation of molecular acetic acid species leaving adsorbed acetate. At 440 K, decomposition of the acetate species occurs via decarbonylation and decarboxylation as evidenced by desorption peaks for H₂,CO, CO₂ and CHX fragments (x=1, 2) in theTPD.The assignments for the experimental IR peaks were made using visualization of the DFT-calculated vibrational modes. The results showed that acetate adsorbs in a bridged bidentate (μ²η²(O,O)) configuration. The coexistence of linear and bridge bonded CO was also predicted by the DFT results. Similar molecular acid adsorption energy was predicted in the case of Ni(111) whereas a significant difference was found for acetate adsorption. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=acetic%20acid" title="acetic acid">acetic acid</a>, <a href="https://publications.waset.org/abstracts/search?q=platinum" title=" platinum"> platinum</a>, <a href="https://publications.waset.org/abstracts/search?q=nickel" title=" nickel"> nickel</a>, <a href="https://publications.waset.org/abstracts/search?q=infared-absorption%20spectrocopy" title=" infared-absorption spectrocopy"> infared-absorption spectrocopy</a>, <a href="https://publications.waset.org/abstracts/search?q=temperature%20programmed%20desorption" title=" temperature programmed desorption"> temperature programmed desorption</a>, <a href="https://publications.waset.org/abstracts/search?q=density%20functional%20theory" title=" density functional theory"> density functional theory</a> </p> <a href="https://publications.waset.org/abstracts/147988/acetic-acid-adsorption-and-decomposition-on-pt111-comparisons-to-ni111" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/147988.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">108</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">3</span> Fermentable Bio-Ethanol Using Bakers and Palmwine Yeasts: Indices of Bioavailability of Carbohydrate and Sugar from Fungal Treated Rice Husk</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ezeonu">Ezeonu</a>, <a href="https://publications.waset.org/abstracts/search?q=Chukwuma%20Stephen"> Chukwuma Stephen</a>, <a href="https://publications.waset.org/abstracts/search?q=Onwurah"> Onwurah</a>, <a href="https://publications.waset.org/abstracts/search?q=Ikechukwu%20Noel%20Emmanuel"> Ikechukwu Noel Emmanuel</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Pure strains of Aspergillus fumigatus (AF), aspergillus niger (AN), aspergillus oryzae (AO), trichophyton mentagrophyte (TM), trichophyton rubrum (TR) and Trichophyton soudanense (TS) were isolated from decomposing rice husk. Freshly processed rice husk in Mandle’s medium were heat pre-treated using an autoclave at 121oC for 20 minutes. The isolated fungi as monoculture and di-culture combinations were inoculated into each of the pre-treated rice husk with the exception of two controls. Seven days hydrolysis was followed by estimation of carbohydrate, reducing sugar and non-reducing sugar. Fungal treated rice husks were left to ferment for 7 days with introduction of both baker’s and palm wine yeast. The result obtained in the work gave the highest carbohydrate (20.53 ± 2.73 %) from rice husks treated with TS + TR di-culture. The highest soluble reducing sugar (2.66 ± 0.14 %) was obtained from rice husk treated with TM. The highest soluble nonreducing sugar (18.08 ± 2.61 %) was from AF. The introduction of yeasts from palm wine gave the highest bio-ethanol (12.82 ± 0.39 %) from AO. The highest bio-ethanol (6.60 ± 0.10 %) from baker's yeast fermentation was in AO + TS treated rice husk. There was increased availability of sugar and moderate yield of bio-ethanol, especially from palm wine yeast. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=fungi" title="fungi">fungi</a>, <a href="https://publications.waset.org/abstracts/search?q=rice%20husk" title=" rice husk"> rice husk</a>, <a href="https://publications.waset.org/abstracts/search?q=carbohydrate" title=" carbohydrate"> carbohydrate</a>, <a href="https://publications.waset.org/abstracts/search?q=reducing%20sugar" title=" reducing sugar"> reducing sugar</a>, <a href="https://publications.waset.org/abstracts/search?q=non-reducing%20sugar" title=" non-reducing sugar"> non-reducing sugar</a>, <a href="https://publications.waset.org/abstracts/search?q=ethanol" title=" ethanol"> ethanol</a>, <a href="https://publications.waset.org/abstracts/search?q=fermentation" title=" fermentation"> fermentation</a> </p> <a href="https://publications.waset.org/abstracts/27558/fermentable-bio-ethanol-using-bakers-and-palmwine-yeasts-indices-of-bioavailability-of-carbohydrate-and-sugar-from-fungal-treated-rice-husk" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/27558.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">440</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2</span> Optimization of Biomass Components from Rice Husk Treated with Trichophyton Soudanense and Trichophyton Mentagrophyte and Effect of Yeast on the Bio-Ethanol Yield</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Chukwuma%20S.%20Ezeonu">Chukwuma S. Ezeonu</a>, <a href="https://publications.waset.org/abstracts/search?q=Ikechukwu%20N.%20E.%20Onwurah"> Ikechukwu N. E. Onwurah</a>, <a href="https://publications.waset.org/abstracts/search?q=Uchechukwu%20U.%20Nwodo"> Uchechukwu U. Nwodo</a>, <a href="https://publications.waset.org/abstracts/search?q=Chibuike%20S.%20Ubani"> Chibuike S. Ubani</a>, <a href="https://publications.waset.org/abstracts/search?q=Chigozie%20M.%20Ejikeme"> Chigozie M. Ejikeme</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Trichophyton soudanense and Trichophyton mentagrophyte were isolated from the rice mill environment, cultured and used singly and as di-culture in the treatment of measure quantities of preheated rice husk. Optimized conditions studied showed that carboxymethylcellulase (CMCellulase) activity of 57.61 µg/ml/min was optimum for Trichophyton mentagrophyte heat pretreated rice husk crude enzymes at 50oC and 80oC respectively. Duration of 120 hours (5 days) gave the highest CMcellulase activity of 75.84 µg/ml/min for crude enzyme of Trichophyton mentagrophyte heat pretreated rice husk. However, 96 hours (4 days) duration gave maximum activity of 58.21 µg/ml/min for crude enzyme of Trichophyton soudanense heat pretreated rice husk. Highest CMCellulase activities of 67.02 µg/ml/min and 69.02 µg/ml/min at pH of 5 were recorded for crude enzymes of monocultures of Trichophyton soudanense (TS) and Trichophyton mentagrophyte (TM) heat pretreated rice husk respectively. Biomass components showed that rice husk cooled after heating followed by treatment with Trichophyton mentagrophyte gave 44.50 ± 10.90 (% ± Standard Error of Mean) cellulose as the highest yield. Maximum total lignin value of 28.90 ± 1.80 (% ± SEM) was obtained from pre-heated rice husk treated with di-culture of Trichophyton soudanense and Trichophyton mentagrophyte (TS+TM). The hemicellulose content of 30.50 ± 2.12 (% ± SEM) from pre-heated rice husk treated with Trichophyton soudanense (TS); lignin value of 28.90 ± 1.80 from pre-heated rice husk treated with di-culture of Trichophyton soudanense and Trichophyton mentagrophyte (TS+TM); also carbohydrate content of 16.79 ± 9.14 (% ± SEM) , reducing and non-reducing sugar values of 2.66 ± 0.45 and 14.13 ± 8.69 (% ± SEM) were all obtained from for pre- heated rice husk treated with Trichophyton mentagrophyte (TM). All the values listed above were the highest values obtained from each rice husk treatment. The pre-heated rice husk treated with Trichophyton mentagrophyte (TM) fermented with palmwine yeast gave bio-ethanol value of 11.11 ± 0.21 (% ± Standard Deviation) as the highest yield. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Trichophyton%20soudanense" title="Trichophyton soudanense">Trichophyton soudanense</a>, <a href="https://publications.waset.org/abstracts/search?q=Trichophyton%20mentagrophyte" title=" Trichophyton mentagrophyte"> Trichophyton mentagrophyte</a>, <a href="https://publications.waset.org/abstracts/search?q=biomass" title=" biomass"> biomass</a>, <a href="https://publications.waset.org/abstracts/search?q=bioethanol" title=" bioethanol"> bioethanol</a>, <a href="https://publications.waset.org/abstracts/search?q=rice%20husk" title=" rice husk"> rice husk</a> </p> <a href="https://publications.waset.org/abstracts/27579/optimization-of-biomass-components-from-rice-husk-treated-with-trichophyton-soudanense-and-trichophyton-mentagrophyte-and-effect-of-yeast-on-the-bio-ethanol-yield" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/27579.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">679</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1</span> Advances in the Studies on Evaluation of Diversity and Habitat Preferences of Amphibians of Nigeria</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Md%20Mizanur%20Rahman">Md Mizanur Rahman</a>, <a href="https://publications.waset.org/abstracts/search?q=Lotanna%20Micah%20Nneji"> Lotanna Micah Nneji</a>, <a href="https://publications.waset.org/abstracts/search?q=Adeola%20C.%20Adeniyi"> Adeola C. Adeniyi</a>, <a href="https://publications.waset.org/abstracts/search?q=Edem%20Archibong%20Eniang"> Edem Archibong Eniang</a>, <a href="https://publications.waset.org/abstracts/search?q=Abiodun%20B.%20Onadeko"> Abiodun B. Onadeko</a>, <a href="https://publications.waset.org/abstracts/search?q=Felista%20Kasyoka%20Kilunda"> Felista Kasyoka Kilunda</a>, <a href="https://publications.waset.org/abstracts/search?q=Babatunde%20E.%20Adedeji"> Babatunde E. Adedeji</a>, <a href="https://publications.waset.org/abstracts/search?q=Ifeanyi%20C.%20Nneji"> Ifeanyi C. Nneji</a>, <a href="https://publications.waset.org/abstracts/search?q=Adiaha%20A.%20A.%20Ugwumba"> Adiaha A. A. Ugwumba</a>, <a href="https://publications.waset.org/abstracts/search?q=Jie-Qiong%20Jin"> Jie-Qiong Jin</a>, <a href="https://publications.waset.org/abstracts/search?q=Min-Sheng%20Peng"> Min-Sheng Peng</a>, <a href="https://publications.waset.org/abstracts/search?q=Caroline%20Olory"> Caroline Olory</a>, <a href="https://publications.waset.org/abstracts/search?q=Nsikan%20Eninekit"> Nsikan Eninekit</a>, <a href="https://publications.waset.org/abstracts/search?q=Jing%20Che"> Jing Che</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Nigeria contains a number of forest habitats that believed to host highly rich amphibian diversity. However, a dearth of herpetological studies has restricted information on the amphibian diversity in Nigeria. To cover the gap of knowledge, this study focused field surveys on relatively less studied forests–Afi Forest Reserve and Ikpan forest ecosystem. The goal of this study is to make a checklist and to investigate the habitat preferences of amphibians in these two forests. The study areas were surveyed between August 2018 and July 2019 following visual and acoustic methods. Individuals were identified using the morphological and molecular (16S ribosomal RNA) approach. Literature searches were conducted to document additional species that were not encountered during the current field surveys. Using the observational records and arrays of diversity indices, the patterns of species richness and abundance across habitat types were evaluated. Voucher specimens and tissue samples were deposited in the museums of the Department of Zoology, University of Ibadan Nigeria, and the remainder at the Kunming Institute of Zoology (KIZ), Chinese Academy of Sciences, Kunming, China. The result of this study revealed the presence of 30 and 31 amphibian species from the Afi Forest Reserve and the Ikpan Forest Ecosystem, respectively. There were two unidentified species from AFR and one from IFE. In total, 324 individuals of amphibian species were observed from the two study areas. Forest and swamps showed high species diversity and richness than the agricultural field and savannah. Savannah and agricultural fields had the highest similarity in the species composition. Given the increased human disturbances and consequent threats to these forests, this study offers recommendations for the initiation of conservation plans immediately. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biodiversity" title="biodiversity">biodiversity</a>, <a href="https://publications.waset.org/abstracts/search?q=conservation" title=" conservation"> conservation</a>, <a href="https://publications.waset.org/abstracts/search?q=cryptic%20species" title=" cryptic species"> cryptic species</a>, <a href="https://publications.waset.org/abstracts/search?q=ecology" title=" ecology"> ecology</a>, <a href="https://publications.waset.org/abstracts/search?q=integrated%20taxonomy" title=" integrated taxonomy"> integrated taxonomy</a>, <a href="https://publications.waset.org/abstracts/search?q=species%20inventory" title=" species inventory"> species inventory</a> </p> <a href="https://publications.waset.org/abstracts/119663/advances-in-the-studies-on-evaluation-of-diversity-and-habitat-preferences-of-amphibians-of-nigeria" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/119663.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">167</span> </span> </div> </div> </div> </main> <footer> <div id="infolinks" class="pt-3 pb-2"> <div class="container"> <div style="background-color:#f5f5f5;" class="p-3"> <div class="row"> <div class="col-md-2"> <ul class="list-unstyled"> About <li><a href="https://waset.org/page/support">About Us</a></li> <li><a href="https://waset.org/page/support#legal-information">Legal</a></li> <li><a target="_blank" rel="nofollow" href="https://publications.waset.org/static/files/WASET-16th-foundational-anniversary.pdf">WASET celebrates its 16th foundational anniversary</a></li> 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