Academic literature on the topic 'Bio-Based fatty acids'
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Journal articles on the topic "Bio-Based fatty acids"
Stavila, Erythrina, Frita Yuliati, Azis Adharis, Joddy Arya Laksmono, and Muhammad Iqbal. "Recent advances in synthesis of polymers based on palm oil and its fatty acids." RSC Advances 13, no. 22 (2023): 14747–75. http://dx.doi.org/10.1039/d3ra01913f.
Full textFrihart, Charles R. "Chemistry of Dimer Acid Production from Fatty Acids and the Structure–Property Relationships of Polyamides Made from These Dimer Acids." Polymers 15, no. 16 (August 9, 2023): 3345. http://dx.doi.org/10.3390/polym15163345.
Full textMensah, Joel B., Adrian H. Hergesell, Sebastian Brosch, Christiane Golchert, Jens Artz, and Regina Palkovits. "Catalytic deoxygenation of bio-based 3-hydroxydecanoic acid to secondary alcohols and alkanes." Green Chemistry 22, no. 11 (2020): 3522–31. http://dx.doi.org/10.1039/d0gc00691b.
Full textMcDowall, Stewart Charles, Maria Braune, and Roy Nitzsche. "Recovery of bio-based medium-chain fatty acids with membrane filtration." Separation and Purification Technology 286 (April 2022): 120430. http://dx.doi.org/10.1016/j.seppur.2021.120430.
Full textBeller, Harry R., Taek Soon Lee, and Leonard Katz. "Natural products as biofuels and bio-based chemicals: fatty acids and isoprenoids." Natural Product Reports 32, no. 10 (2015): 1508–26. http://dx.doi.org/10.1039/c5np00068h.
Full textNarra, Naganna, Badari Narayana Prasad Rachapudi, Sahithya Phani Babu Vemulapalli, and Padmaja V. Korlipara. "Lewis-acid catalyzed synthesis and characterization of novel castor fatty acid-based cyclic carbonates." RSC Advances 6, no. 31 (2016): 25703–12. http://dx.doi.org/10.1039/c6ra00880a.
Full textSimar-Mentières, S., F. Nesslany, M. L. Sola, S. Mortier, J. M. Raimbault, F. Gondelle, L. Chabot, P. Pandard, D. Wils, and A. Chentouf. "Toxicology and Biodegradability of a Phthalate-Free and Bio-Based Novel Plasticizer." Journal of Toxicology 2021 (July 12, 2021): 1–15. http://dx.doi.org/10.1155/2021/9970896.
Full textLamarzelle, Océane, Geoffrey Hibert, Sébastien Lecommandoux, Etienne Grau, and Henri Cramail. "A thioglycerol route to bio-based bis-cyclic carbonates: poly(hydroxyurethane) preparation and post-functionalization." Polymer Chemistry 8, no. 22 (2017): 3438–47. http://dx.doi.org/10.1039/c7py00556c.
Full textHe, Songbo, Thomas Sjouke Kramer, Dian Sukmayanda Santosa, Andre Heeres, and Hero Jan Heeres. "Catalytic conversion of glycerol and co-feeds (fatty acids, alcohols, and alkanes) to bio-based aromatics: remarkable and unprecedented synergetic effects on catalyst performance." Green Chemistry 24, no. 2 (2022): 941–49. http://dx.doi.org/10.1039/d1gc03531b.
Full textKulomaa, Tuomas, Jorma Matikainen, Pirkko Karhunen, Mikko Heikkilä, Juha Fiskari, and Ilkka Kilpeläinen. "Cellulose fatty acid esters as sustainable film materials – effect of side chain structure on barrier and mechanical properties." RSC Advances 5, no. 98 (2015): 80702–8. http://dx.doi.org/10.1039/c5ra12671a.
Full textDissertations / Theses on the topic "Bio-Based fatty acids"
Torella, Joseph Peter. "Synthetic biology approaches to bio-based chemical production." Thesis, Harvard University, 2014. http://nrs.harvard.edu/urn-3:HUL.InstRepos:13088835.
Full textJin, Yuqin. "Biotechnological improvements of bio-based fuels and lubricants characterization of genes for branched chain fatty acids and mono-acyl esters /." [Ames, Iowa : Iowa State University], 2007.
Find full textLorenzen, Jan [Verfasser], Thomas [Akademischer Betreuer] Brück, Thomas [Gutachter] Brück, Thomas [Gutachter] Fässler, Uwe [Gutachter] Bornscheuer, and Wolfgang [Gutachter] Eisenreich. "Enzymatic functionalization of bio based fatty acids and algae based triglycerides / Jan Lorenzen ; Gutachter: Thomas Brück, Thomas Fässler, Uwe Bornscheuer, Wolfgang Eisenreich ; Betreuer: Thomas Brück." München : Universitätsbibliothek der TU München, 2019. http://d-nb.info/1201819997/34.
Full textClaudino, Mauro. "Thiol−ene Coupling of Renewable Monomers : at the forefront of bio-based polymeric materials." Licentiate thesis, KTH, Ytbehandlingsteknik, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-40267.
Full textVegetabiliska oljor som innehåller dubbelbindningar kan användas direkt för thiolene reaktioner. Trots att terminala dubbelbindningar är mycket mer reaktiva än interna visar dessa studier att den reversibla additionen av thiyl radikaler till 1,2-disubstituerade alkener är en viktig reaktion. För att undersöka tiol–ene reaktionerna, som ivolverar dessa alkener förbereddes stökiometriska blandningar av en trifunktionell propionat tiol och enkelomättade fettsyrametylestrar (metyloleat eller metyl elaidat) samt 2.0 vikt.% Irgacure 184. Dessa blandningar utsattes för 365-nm UV strålning och de kemiska förändringarna studerades. De kemiska förändringarna analyserades med olika kemiska analysmetoder; realtid RT–FTIR, NMR och FT–Raman. Dessa användes för att analysera de kemiska reaktionerna i realtid och följa bildandet av produkterna. Reaktionsmekanismen bekräftades med hjälp av experimentella data och beräkningar av numeriska och kinetiska simuleringar för systemet. Resultaten visar en mycket snabb cis/trans-isomerisering av alkenmonomeren (<1.0 min) jämfört med den totala förbrukningen av dubbelbindningarna, vilket indikerar att det hastighetsbegränsande steget kontrolleras av väteförflyttningen från tiolen till slutprodukten. Förbrukningen av den totala omättade kolkedjan är lika med tiolförbrukningen under hela reaktionen, även om bildandet av produkten gynnas från trans-enen. Detta indikerar att den första cis/trans-isomerstrukturen påverkar kinetiken. Höga tiol-ene utbyten kan enkelt erhållas relativt snabbt utan inverkan av sidoreaktioner. Detta innebär att denna reaktion kan användas som nätverksbildande reaktion för flerfunktionella 1,2-disubstituted alkenmonomerer. Vidare användes fotopolymerisation i smälta på en serie globalid/kaprolaktonbaserade sampolyestrar med varierad grad av omättnad med samma tritiol vilket resulterade i bildandet av amorfa elastomeriska material med olika termiska och viskoelastiska egenskaper. Hög omsättning (>80%) uppnåddes relativt enkelt för samtliga blandningar oberoende av den initiala funktionaliteten. Homopolymerisation av alkenen var försumbar i jämförelse med den tiol–en-reaktionen. Mängden alkengrupper har inverkan på härdplastsegenskaperna där en hög andel alken ger en nätstruktur med högre glastransitionstemperatur (Tg). Tiol–ene reaktionen utvärderades i modellsystem baserade på naturlig förekommande 1,2-disubstituterade alkener för att demonstrera konceptet med tiol-förnätade halvsyntetiska material.
QC 20110915
Zhao, Huiping. "I. Total synthesis of [plus or minus] ovalicin and its analogues II. Bio-based polymers from vegetable oilIII. New synthetic methods of diacetylene fatty acids." Manhattan, Kan. : Kansas State University, 2008. http://hdl.handle.net/2097/735.
Full textZhao, Huiping. "I. Total synthesis of [plus or minus] ovalicin and its analogues II. Bio-based polymers from vegetable oil III. New synthetic methods of diacetylene fatty acids." Diss., Kansas State University, 2008. http://hdl.handle.net/2097/735.
Full textDepartment of Chemistry
Duy H. Hua
I. Ovalicin is a natural product isolated from the culture of fungus Pseudorotium ovalis Stolk, it selectively inhibit type 2 methionine amino-peptidase (MetAP 2), which related to many physiological activities such as angiogenesis. Total synthesis of [plus or minus] ovalicin, its C4(S*), C4(S*)C5(S*) stereo-isomers, and C5 regio-isomer were synthesized via an intramolecular Heck reaction of (Z)-3-(t-butyldimethyl silyloxy)-1-iodo-1,6-heptadiene utilizing a catalytic amount of palladium acetate. Subsequent epoxidation, dihydroxylation, methylation (or stereochemistry inversion before or after methylation) and oxidation led to a variety of ketones, key intermediates for synthesis of ovalicin and its analogues. Introduction of side-chain to ketones by lithium (Z)-6-methylhepta-2,5-dien-2-ide and following functional group transformation led to ovalicin and its analogues. Anti-trypanosomal activities of various ovalicin analogues and synthetic intermediates were evaluated. II. Bio-based polymers from vegetable oils are renewable and environment-friendly materials. Dihydroxylated, trihydroxylate, tetrahydroxylated and hexahydroxylated triglycerides, triamino and triisopropylamino glycerides were synthesized from model triglyceride glyceryl trioleoate. These monomers were cross-linked with 1, 4-phenylene diisocynate to make polyurethanes and polyureas. The physical properties of these polymers were examined by gel content and swelling value measurements, thermodynamic and viscoelastic properties were studied from TGA, DSC and DMA measurements. The structure-property relationship was discussed based on these measurements. III. Diacetylenic fatty acids were widely applied in material science to regulate alignment on surface and stabilize self-assembled nanomaterials. A novel synthetic method of diacetylenic fatty acids from vegetable oils was developed. Its self-assembling properties on alumina surface were measured and discussed.
Fortier, Lucas. "Réactivité de la fonction acide carboxylique en catalyse photoredox : applications à la valorisation d'acides gras biosourcés." Electronic Thesis or Diss., Université de Lille (2022-....), 2024. http://www.theses.fr/2024ULILR068.
Full textThis thesis contributes to the development of more environmentally friendly chemical processes, addressing current environmental challenges. It explores the use of bio-based molecules and eco-responsible syntheses, focusing on photocatalysis, rapidly expanding approaches. The research centers on the potential of carboxylic acids in photoredox catalysis for synthesizing valuable organic compounds, offering alternatives to conventional methods that are often energy-intensive and less environmentally friendly. The thesis is structured into three main chapters. The first provides a theoretical introduction to photocatalysis, covering its principles and recent advances. The second chapter develops two novel decarboxylative C-C coupling methods between fatty acids and radical acceptors, aimed at producing monomers for biobased polymers and surfactants. This process leverages bio-based fatty acids as an alternative to petroleum-derived precursors, adhering to green chemistry principles and aiming for sustainable production of functional molecules. The third chapter explores the synthesis of phthalides, compounds with significant biological and pharmacological properties, using mild photocatalytic conditions. This approach avoids more energy-intensive methods and relies on organic catalysts to optimize reaction efficiency and selectivity. This work represents an advancement in organic and materials chemistry, with applications for bio-based polymer production and the creation of new chemicals. It also opens avenues for further improvement, particularly by exploring the use of infrared light to activate reactions under even milder conditions
Maisonneuve, Lise. "Vegetable oils as a platform for the design of sustainable and non-isocyanate thermoplastic polyurethanes." Thesis, Bordeaux 1, 2013. http://www.theses.fr/2013BOR15218/document.
Full textThis thesis aims to synthesize more sustainable thermoplastic polyurethanes from vegetable oil derivatives. The first route that has been investigated is based on the well-known reaction between a diol and a diisocyanate. Then to avoid the use of diisocyanates, the route via the polyaddition of a bis cyclic carbonate and a diamine have been studied as well. For this purpose, bifunctional precursors such as diols, bis 5- and 6-membered cyclic carbonates and diamines have been prepared from sunflower oil derivative (methyl oleate) and castor oil derivatives (methyl undecenoate and sebacic acid) The thermo-mechanical properties of the PUs have been modulated by designing and selecting the chemical structure of the (fatty acid-based) monomers. The performed model reaction kinetics revealed the higher reactivity of the 6-membered cyclic carbonates compare to the 5-membered ones. Finally, the developed route to fatty acid-based diamines via dinitriles synthesis in mild conditions was really efficient and this route is really promising to develop a fatty acid based-diamines platform and fully bio-based poly(hydroxyurethane)s
Chemin, Maud. "Valorisation des xylanes du bois : vers la synthèse de copolymères amphiphiles bio-sourcés." Thesis, Bordeaux, 2014. http://www.theses.fr/2014BORD0302/document.
Full textThis thesis work aims to add value to xylans by designing new bio-based amphiphilic polymers.Beechwood xylans were first fully characterized before their acidic hydrolysis. The hydrolysis conditions were optimized in order to obtain well-defined xylooligosaccharides, oligomeric chains of about six xylose units that have only one methylglucuronic acid unit positioned at the non-reductive chain end. Periodate oxidation of xylans was also studied in order to form new aldehyde groups within the xylan backbone in a controlled manner. The xylooligomers were then functionalized from their reductive end with an azide or an allyl group, providing the ability to couple these oligomers to fatty acid derivatives using ‘click chemistry’.The obtained amphiphilic oligomers were finally studied according to their surfactant and self-assembly properties. Their wetting properties were found to be very good, comparable to those found with Tween®80. Moreover, they self-assembled in both chloroform and water, where their structures were characterized via DLS and TEM. The resulting particles formed had a spherical micellar morphology, with a d ≤ 50 nm. However, it was found that the particles had a tendency to form large aggregates, particularly in chloroform. The aggregates could be easily removed, either by filtration or by dilution of the sample, as the forces that govern the aggregation are low enough to allow dissociation with increasing solvent volume.As previously mentioned, this thesis work led to the synthesis of bio-based amphiphilic oligomers starting from xylans, which are a potential byproduct in the paper/pulp industry. Thanks to their surfactant properties, numerous applications can be found for such a ‘green’ surfactant. Their biocompatibility added with their self-assembly nature in aqueous media makes them an attractive molecule for active substance delivery applications
Pereira, Beatriz D’Avó. "Development of bio-based nanoemulsions to improve physical and chemical stability of omega-3 fatty acids." Master's thesis, 2017. http://hdl.handle.net/1822/55570.
Full textNowadays there is a high interest by the food industry to develop nutritional food products. This concept promoted the development of bio-based structures to encapsulate bioactive compounds and thus enhance their physical and chemical stability from storage up until consumption. Omega-3 (ω-3) is known for its functional properties such as improving cardiovascular health, decrease inflammation, increase cognitive function. However, ω-3 fatty acids are highly susceptible to oxidation, have intense odour and low water solubility, which makes its direct application in foods extremely difficult. In order to reduce these problems, nanoencapsulation, through nanoemulsions can be used. With this in mind, lactoferrin (Lf), a protein derived from milk with a wide range of reported biological activities (e.g. antioxidant, antimicrobial, cancer prevention) was used as natural emulsifier for the development of oil-in-water nanoemulsions for ω-3 encapsulation. The nanoemulsions were characterized and assessed by physical and chemical stability during storage. Nanoemulsions were also dried by freeze-drying and nanospray-drying and further characterized. ω-3 nanoemulsions were successfully produced through high pressure homogenization, with results showing that the concentration of Lf influenced size and superficial charge of the nanoemulsions droplets obtained. Nanoemulsions revealed physical stability when stored at 4 ºC for 69 days, while presenting instability at room temperature. The antioxidant capacity of the nanoemulsions did not show significative alterations over storage while a significative increase in oxidation was registered. Only the nanoemulsions dried by nanopray-drying presented defined structures. The rehydration of the powders resulted from freeze-drying was possible while powders obtained by nanospray-drying were not able to be rehydrated. Overall the results suggest that ω-3 nanoemulsions with physical stability can be produced using Lf while chemical stability was not achieved. The Lf nanoemulsions can also be dried to obtain powders with defined submicron particles but its rehydration its limited. This work provides important information that can be useful for the design of nanoemulsions and dry capsules aiming the encapsulation of lipophilic compounds for pharmaceutical and food applications.
Hoje em dia existe um grande interesse da industria alimentar no desenvolvimento de produtos alimentares com elevado valor nutricional. Este conceito tem promovido o desenvolvimento de estruturas de origem natural para encapsular compostos bio-ativos, permitindo melhorar a sua estabilidade química e física, desde o armazenamento até ao seu consumo. O ómega-3 (ω-3) apresenta importantes propriedades funcionais tais como a melhoria de saúde cardiovascular, diminuição de inflamação, aumento de funções cognitivas. No entanto, é extremamente suscetível a oxidação, tem um odor intenso e uma baixa solubilidade em água, o que faz com que a sua aplicação direta em alimentos seja extremamente difícil. A nanoencapsulação deste composto surge como uma alternativa para solucionar tais problemas. A Lactoferrina (Lf) uma proteína derivada do leite, com inúmeras propriedades biológicas (p.e. antioxidante, antimicrobiana, prevenção de cancro) foi usada como emulsionante natural na produção de nanoemulsões óleo-em-água para a encapsulação de ω-3, as quais foram posteriormente caracterizadas e avaliadas a nível da estabilidade física e química durante o armazenamento. Estas foram ainda submetidas a 2 diferentes processos de secagem (liofilização e nanaopray-drying). Produziram-se com sucesso nanoemulsões através de homogeneização de alta pressão, tendo-se verificado que a concentração de Lf influencia o seu tamanho e carga superficial. As nanoemulsões, revelaram estabilidade física quando armazenadas (69 dias) a 4 ºC, mas não quando armazenadas à temperatura ambiente. A capacidade antioxidante, quando armazenadas (4 ºC durante 35 dias), não apresentou alterações significativas, enquanto que os valores de oxidação aumentaram. Apenas as nanoemulsões submetidas ao processo de nanaopray-drying apresentaram uma estrutura resultante bem definida, e apenas as nanoemulsões submetidas ao processo de liofilização foram possíveis de ser rehidratadas. A presente tese permitiu verificar que nanoemulsões de ω-3, com estabilidade física, podem ser produzidas, usando Lf, no entanto não foi possível obter estabilidade química. A sua secagem permite a obtenção de estruturas definidas. Este trabalho permitiu obter informação relevante para o desenvolvimento de nanoemulsões que tenham como objetivo a encapsulação de compostos lipofílicos para aplicações alimentares e farmacêuticas.
Book chapters on the topic "Bio-Based fatty acids"
Ngo, Helen, Karen Wagner, Alberto Nuñez, Jianwei Zhang, Xuetong Fan, and Robert A. Moreau. "New Classes of Antimicrobials: Poly-Phenolic Branched-Chain Fatty Acids." In Natural and Bio-Based Antimicrobials for Food Applications, 209–21. Washington, DC: American Chemical Society, 2018. http://dx.doi.org/10.1021/bk-2018-1287.ch011.
Full textWiedemann, Sophie C. C., Pieter C. A. Bruijnincx, and Bert M. Weckhuysen. "Isostearic Acid: A Unique Fatty Acid with Great Potential." In Chemicals and Fuels from Bio-Based Building Blocks, 51–78. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527698202.ch3.
Full textShafi, Wani Khalid, M. S. Charoo, and M. Hanief. "Effect of Fatty Acid Composition on the Lubricating Properties of Bio-Based Green Lubricants." In Tribology and Sustainability, 231–50. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003092162-16.
Full textBie, Xiaomei. "Fengycin Production and Its Applications in Plant Growth and Postharvest Quality." In Bio-Based Antimicrobial Agents to Improve Agricultural and Food Safety, 71–119. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815256239124010006.
Full textWebster, Dean C. "Bio-based Polymers and Resins in Paints and Coatings." In Bioplastics and Biocomposites, 249–73. Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781788010085-00249.
Full textOnat, B. "Applications of SPME for the Determination of Amino Acids and Peptides in Biological Matrices." In Evolution of Solid Phase Microextraction Technology, 441–50. The Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781839167300-00441.
Full textAssunção, Joana, Helena M. Amaro, F. Xavier Malcata, and A. Catarina z. Guedes. "Extraction of Microalgal Bioactive Compounds Towards Functional Ingredients: A Biorefinery Approach with Prospects And Challenges." In Algal Functional Foods and Nutraceuticals: Benefits, Opportunities, and Challenges, 131–83. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815051872122010011.
Full textConference papers on the topic "Bio-Based fatty acids"
Ramasamy, Jothibasu, and Mohammad K. Arfaj. "Sustainable and Eco-Friendly Drilling Fluid Additives Development." In International Petroleum Technology Conference. IPTC, 2022. http://dx.doi.org/10.2523/iptc-22455-ms.
Full textRamasamy, Jothibasu, and Mohammad K. Arfaj. "Sustainable and Green Drilling Fluid Additives Development." In Offshore Technology Conference Asia. OTC, 2022. http://dx.doi.org/10.4043/31350-ms.
Full textKulshreshtha, Yask, Philip J. Vardon, Gabrie Meesters, Mark C. M. van Loosdrecht, Nelson J. A. Mota, and Henk M. Jonkers. "What Makes Cow-Dung Stabilised Earthen Block Water-Resistant." In 4th International Conference on Bio-Based Building Materials. Switzerland: Trans Tech Publications Ltd, 2022. http://dx.doi.org/10.4028/www.scientific.net/cta.1.540.
Full textEichenauer, Sabrina, Bernd Weber, and Ernst A. Stadlbauer. "Thermochemical Processing of Animal Fat and Meat and Bone Meal to Hydrocarbon Based Fuels." In ASME 2015 9th International Conference on Energy Sustainability collocated with the ASME 2015 Power Conference, the ASME 2015 13th International Conference on Fuel Cell Science, Engineering and Technology, and the ASME 2015 Nuclear Forum. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/es2015-49197.
Full textCaillol, Sylvain. "Plant oil based radically polymerizable monomers for sustainable polymers." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/kypx2569.
Full textObuebite, A., and O. O. Okwonna. "Preliminary Assessment of Terminalia Mantaly Gum Exudate as a GreenScale Inhibitor." In SPE Nigeria Annual International Conference and Exhibition. SPE, 2024. http://dx.doi.org/10.2118/221793-ms.
Full textRahayu, Sri, Supriyatin, and Adiati Bintari. "Activated carbon-based bio-adsorbent for reducing free fatty acid number of cooking oil." In THE 9TH INTERNATIONAL CONFERENCE ON GLOBAL RESOURCE CONSERVATION (ICGRC) AND AJI FROM RITSUMEIKAN UNIVERSITY. Author(s), 2018. http://dx.doi.org/10.1063/1.5061897.
Full textCatalanotti, E., K. J. Hughes, M. Pourkashanian, I. Uryga-Bugajska, and A. Williams. "Development of a High Temperature Oxidation Mechanism for Bio-Aviation Fuels." In ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-68667.
Full textMurali Krishna, B., and J. M. Mallikarjuna. "Renewable Biodiesel From CSO: A Fuel Option for Diesel Engines." In ASME 2006 International Solar Energy Conference. ASMEDC, 2006. http://dx.doi.org/10.1115/isec2006-99051.
Full textNiemi, Seppo, Jukka Kiijärvi, Mika Laurén, and Erkki Hiltunen. "Injection Pressures of a Bio-Oil Driven Non-Road Diesel Engine: Experiments and Simulations." In ASME 2012 11th Biennial Conference on Engineering Systems Design and Analysis. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/esda2012-82710.
Full textReports on the topic "Bio-Based fatty acids"
Mattie, David R., Jonathon M. Hurley, Edward S. Riccio, and Teresa R. Sterner. Acute Dermal Irritation Study and Salmonella-Escherichia coli/Microsome Plate Incorporation Assay of Hydroprocessed Esters and Fatty Acids (HEFA) Bio-Based Jet Fuels. Fort Belvoir, VA: Defense Technical Information Center, January 2013. http://dx.doi.org/10.21236/ada584649.
Full textWong, Brian A., William R. Howard, Teresa R. Sterner, Michelle W. Elliott, and David R. Mattie. 90-Day Inhalation Toxicity Study of Hydroprocessed Esters and Fatty Acids (HEFA) Bio-Based Jet Fuel in Rats (Rattus norvegicus) with Neurotoxicity Testing and Genotoxicity Assay. Fort Belvoir, VA: Defense Technical Information Center, June 2013. http://dx.doi.org/10.21236/ada596005.
Full textGlazer, Itamar, Alice Churchill, Galina Gindin, and Michael Samish. Genomic and Organismal Studies to Elucidate the Mechanisms of Infectivity of Entomopathogenic Fungi to Ticks. United States Department of Agriculture, January 2013. http://dx.doi.org/10.32747/2013.7593382.bard.
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