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Artykuły w czasopismach na temat "Alcohols"
Karkoulias, Kiriakos, Haralampos Tsitsaras, Dimitrios Patouchas, Fotis Sampsonas, Dimostenis Likouras, Alexander Kaparianos i Kostas Spiropoulos. "The alcoholic lung disease: Historical background and clinical features". Medicina 44, nr 9 (22.10.2007): 651. http://dx.doi.org/10.3390/medicina44090084.
Pełny tekst źródłaSolodun, Yuriy, Yulia Monakhova, Thomas Kuballa, Andriy Samokhvalov, Jürgen Rehm i Dirk Lachenmeier. "Unrecorded alcohol consumption in Russia: toxic denaturants and disinfectants pose additional risks". Interdisciplinary Toxicology 4, nr 4 (1.12.2011): 198–205. http://dx.doi.org/10.2478/v10102-011-0030-x.
Pełny tekst źródłaFlorido-Barba, Antonio, Gustavo Cordero-Bueso i Jesús Manuel Cantoral. "Alcoholes no vínicos para la mejora del desarrollo del velo de flor y de las características sensoriales de los vinos Finos de la D.O. Jerez-Xérèz-Sherry". BIO Web of Conferences 68 (2023): 02011. http://dx.doi.org/10.1051/bioconf/20236802011.
Pełny tekst źródłaWang, Ya-Ping, Lin Liu, Xue-Shan Wang, Kun-Qiang Hong, Li-Hua Zhang, Zhong-Guan Sun i Dong-Guang Xiao. "GAT1 Gene, the GATA Transcription Activator, Regulates the Production of Higher Alcohol during Wheat Beer Fermentation by Saccharomyces cerevisiae". Bioengineering 8, nr 5 (8.05.2021): 61. http://dx.doi.org/10.3390/bioengineering8050061.
Pełny tekst źródłaWoo, Kang-Lyung. "Determination of Low MolecularWeight Alcohols Including Fusel Oil in Various Samples by Diethyl Ether Extraction and Capillary Gas Chromatography". Journal of AOAC INTERNATIONAL 88, nr 5 (1.09.2005): 1419–27. http://dx.doi.org/10.1093/jaoac/88.5.1419.
Pełny tekst źródłaGutierrez, L. E. "Effect of some vitamins and micronutrient deficiencies on the production of higher alcohols by Saccharomyces cerevisiae". Scientia Agricola 50, nr 3 (grudzień 1993): 484–89. http://dx.doi.org/10.1590/s0103-90161993000300024.
Pełny tekst źródłaMaia, Amazile Biagioni, Lorena Simão Marinho i David Lee Nelson. "On the role of higher alcohols in the characterization of cachaça". Research, Society and Development 9, nr 10 (21.10.2020): e8299109135. http://dx.doi.org/10.33448/rsd-v9i10.9135.
Pełny tekst źródłaGil, Artyom, Sergey Savchuk, Svetlana Appolonova, Andrey Allenov i Ruslan Khalfin. "AVAILABILITY OF NON-BEVERAGE ALCOHOLS IN RUSSIA IN 2015-2020: WERE CONTROL POLICIES IMPLEMENTED SINCE 2005 EFFECTIVE?" Journal of Law, Public Policies, and Human Sciences 2, nr 2 (20.04.2021): 08–34. http://dx.doi.org/10.52571/jlpphs.v02.n02.pgi.08.2021.
Pełny tekst źródłaWang, Bei, Liu Tao, Yu Cheng, Fang Yang, Yuguang Jin, Chunmei Zhou, Hao Yu i Yanhui Yang. "Electrocatalytic Oxidation of Small Molecule Alcohols over Pt, Pd, and Au Catalysts: The Effect of Alcohol’s Hydrogen Bond Donation Ability and Molecular Structure Properties". Catalysts 9, nr 4 (25.04.2019): 387. http://dx.doi.org/10.3390/catal9040387.
Pełny tekst źródłaBakanov, Vyacheslav Vadimovich, Dmitriy Nikolaevich Vedernikov i Lyubov Sergeevna Khabarova. "EXTRACTIVE SUBSTANCES OF SAPROTROPHIC MUSHROOMS LENTINULA EDODES AND PHOLIOTA SQUARROSA. HEAVY METAL CONTENT". chemistry of plant raw material, nr 3 (22.10.2020): 67–72. http://dx.doi.org/10.14258/jcprm.2020037277.
Pełny tekst źródłaRozprawy doktorskie na temat "Alcohols"
Sumer, Burak. "Synthesis Of 1,2-amino Alcohols Having Tertiary Alcohol Moiety". Master's thesis, METU, 2006. http://etd.lib.metu.edu.tr/upload/12607276/index.pdf.
Pełny tekst źródłaBarroca, Pedro JoseÌ Pereira Marques. "Alcohol oxidase enzymes for the deracemization of secondary alcohols". Thesis, University of Liverpool, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.427019.
Pełny tekst źródłaCornmell, Robert Joseph. "Enantioselective alcohol oxidase enzymes for deracemisation of secondary alcohols". Thesis, University of Liverpool, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.406826.
Pełny tekst źródłaLeonard, Danièle. "Carbonylation of unsaturated alcohols". Thesis, University of Ottawa (Canada), 1986. http://hdl.handle.net/10393/4716.
Pełny tekst źródłaMounzer, Hamza. "Heterogeneous oxidation of alcohols". Thesis, University of Birmingham, 2009. http://etheses.bham.ac.uk//id/eprint/387/.
Pełny tekst źródłaNieuwoudt, Traute. "The separation of alcohols". Thesis, Stellenbosch : Stellenbosch University, 2002. http://hdl.handle.net/10019.1/53172.
Pełny tekst źródłaENGLISH ABSTRACT: Pure primary alcohols are very valuable as raw materials and solvents. Close-boiling alcohol mixtures are produced as byproducts from the Fischer Tropsch synthesis. These byproducts include the mixtures 1-butanol+2- penta noI and 1-pentanol+2-hexanol. Due to the small difference in boiling points these alcohols cannot be separated from one another by using conventional distillation. This study has been undertaken to determine whether primary and secondary alcohols may be separated by exploitation of their chemical properties. Esterification of the alcohols followed by distillation of the esters into cuts and hydrolyses of the esters, has been attempted to separate the alcohols. This however, was unsuccessful. In this study the difference in dehydration rate of secondary and primary alcohols in acidic media has also been investigated. Several acidic resins and liquid catalysts have been used. The acidic resins gave no dehydration or extremely low dehydration rates in the liquid phase. The liquid catalysts H2S04, Oxalic Acid, NaHS04 and H3P04 were investigated. H3P04 gave excellent results. Laboratory experiments were conducted at the boiling point of the reaction mixture at atmospheric pressure. The reaction mixture was sampled at varying time intervals and analysed. The secondary alcohol dehydrated rapidly to the corresponding alkene. The primary alcohol formed symmetrical ethers at a very low rate. The primary and secondary alcohol also combined to form small amounts of unsymmetrical ethers. After the dehydration reaction the organic products can be separated from the acid with a'short path distillation unit. The primary alcohol can further be purified by conventional distillation. Conceptual process designs were done for the separation and purification of the reactor product streams of the alcohol mixtures 1-butanol+2-pentanol and 1-pentanol+2-hexanol. n laboratory scale it was found that for the separation of 85% 1-butanol and 15% 2-pentanol (mass %), 90 % H3P04 (mass %) at an acid:alcohol ratio of 1,5: 1 results in suffcient dehydration of 2-pentanol. A reaction time of 70 minutes is required. A conceptual design on the purification of the 1-butanol predicted a product quality of 99,5 % 1-butanol (mass %) and a 1-butanol recovery of 75 %. The 1-butanol recovery is low, because a major part of the 1-butanol is lost in the purification as part of the ternary azeotrope with water and n-butylether. On laboratory scale it was also found that for the separation of 85 % 1- pentanol+15 % 2-hexanol (mass %),90 % H3P04 (mass %) at an acid:alcohol ratio of 1,5:1 gives sufficient dehydration of 2-hexanol. A reaction time of only 35 minutes is required. A conceptual design on the purification of the 1- pentanol predicted a product quality of 99,9 % 1-pentanol and a 1-pentanol recovery of > 98 %. The 1-pentanol recovery is excellent, only the 1- pentanol that is converted to ethers is lost. In this study it has been proven that a dehydration separation process can be applied successfully to remove secondary alcohols from a primary+secondary alcohol mixture. Especially the removal of 2-hexanol from a 1-pentanol+2- hexanol mixture gave promising results. In order to assess the economic viability of this dehydration process an economic evaluation should be done. This could be part of subsequent studies. The dehydration separation process should be investigated further. It is believed that this dehydration separation process can be expanded to higher alcohols, e.g. 1-hexanol+2-heptanol. It would be extremely advantageous if a solid catalyst could be found for the separation. In this case the recovery of the organics from the reaction mixture would be very much easier. If a solid catatyst is not found, a continuous process using H3P04 as liquid catalyst should be developed.
AFRIKAANSE OPSOMMING: Suiwer primêre alkohole is baie waardevolle rou materiale en oplosmiddels. Alkohol mengsels, wat uit naby-kokende alkohole bestaan, word as neweprodukte in die Fischer Tropsch Sintese gevorm. Hierdie newe-produkte sluit alkohol mengsels soos 1-butanol+2-pentanol en 1-pentanol+2-hexanol in. Weens die klein verskil in kookpunte van hierdie alkohole kan die alkohole nie met konvensionele distillasie van mekaar geskei word nie. Hierdie studie is onderneem om te bepaal of die chemiese eienskappe van alkohole benut kan word om primêre en sekondêre alkohole van mekaar te skei. 'n Poging is aangewend om die alkohole met behulp van esterifikasie te skei. Die alkohole is eers ge-esterifiseer, daarna met behulp van distillasie in verskeie snitte verdeel en die alkohol is vrygestel deur hidrolise van die esters. Dit was egter onsuksesvol. Die verskil in dehidrasie tempo van sekondêre en primêre alkohole in suur mediums is ook ondersoek. Verskeie suur harse en vloeibare kataliste is ondersoek. Die suur .harse het of geen dehidrasie of baie lae dehidrasie tempo's in die vloeistoffase gegee. Die vloeistof kataliste H2S04, Oksaalsuur, NaHS04 en H3P04 is ondersoek. H3P04 het uitstekende resultate gelewer. Eksperimente is op laboratoriumskaal en onder atmosferiese druk uitgevoer. Monsters is van die reaksiemengsels by verskillende tydsintervalle geneem en geanaliseer. Die sekondêre alkohol het vinnig na die ooreenstemmende alkeen gedehidreer. Die primêre alkohole het simmetriese eters teen 'n lae tempo gevorm. Die primêre en sekondêre alkohole het ook gekombineer om gemengde eters te vorm. Kort-pad-distillasie kan gebruik word om na die dehidrase reaksie die organiese produkte van die suur te verwyder. Die primêre alkohole kan verder met konvensionele distillasie gesuiwer word. Konseptueie prosesontwerpe is uitgevoer vir die skeiding en suiwering van die alkohol mengsels 1-butanol+2-pentanol en 1-pentanol+2-hexanol nadat dehidrasie van die mengsels uitgevoer is. Op laboratoriumskaal is dit gevind dat vir die skeiding van 85% 1-butanol en 15% 2-pentanol (massa %), 90 % H3P04 (massa %) met 'n suur:alkohol verhouding van 1,5:1 effektiewe dehidrase van 2-pentanol lewer. fn Reaksietyd van 70 minute word benodig. fn Konseptueie ontwerp vir die suiwering van die 1-butanol het fn produkkwaliteit van 99,5 % 1-butanol (massa %) en fn 1-butanol opbrengs van 75 % voorspel. Die 1-butanol opbrengs is laag aangesien fn groot deel van die 1-butanol verlore gaan as deel van die ternêre azeotroop wat 1-butanol met n-butieleter en water vorm. Dit is ook op laboratoriumskaal vasgestel dat vir die skeiding van 85 % 1- pentanol+15 % 2-hexanol (massa %), 90 % H3P04 (massa %) met fn suur:alkohol verhouding van 1,5:1 effektiewe dehidrase van 2-hexanollewer. fn Reaksietyd van slegs 35 minute word benodig. fn Konseptueie ontwerp vir die suiwering van die 1-pentanol het fn produkkwaliteit van 99,9 % 1-pentanol en fn 1-pentanol opbrengs van > 98 % voorspel. Die 1-pentanol opbrengs is uitstekend, en slegs die 1-pentanol wat omgeskakel word na eters gaan verlore. In hierdie studie is dit bewys dat fn dehidrasie skeidingsproses suksevol aangewend kan word om sekondêre alkohole uit fn primêre+sekondêre alkohol mengsel te verwyder. Veral die verwydering van 2-hexanol uit fn 1- pentanol+2-hexanol mengsel het belowende resultate gelewer. Om die ekonomiese lewensvatbaarheid van so fn skeidingsproses te bepaal moet fn ekonomiese evaluasie van die proses gedoen word. Dit behoort deel van verdere studies te vorm. Die dehidrasie skeidingsproses behoort verder ondersoek te word. Dit word verwag dat die proses na hoër alkohol mengsels, bv. 1-hexanol+2-heptanol uitgebrei kan word. Dit sou baie voordelig wees indien fn geskikte soliede katalis vir die skeiding gevind word. In so fn geval sou die herwinning van die organiese produkte van die reaksiemengsel baie makliker wees. Indien fn soliede katalis nie gevind word nie, behoort fn kontinu proses waarin H3P04 as vloeistof katalis gebruik word, ontwikkel te word.
Gao, Y. (Yun). "Synthesis and synthetic transformations of allylic alcohols, epoxy alcohols, and 1,2-cyclic sulfates". Thesis, Massachusetts Institute of Technology, 1988. http://hdl.handle.net/1721.1/14588.
Pełny tekst źródłaGarcía, Bofill Miquel. "Use of alcohol dehydrogenase and alcohol oxidase to convert alcohols in two valuable products: chlorolactone and vanillin". Doctoral thesis, Universitat Autònoma de Barcelona, 2021. http://hdl.handle.net/10803/673116.
Pełny tekst źródłaLas enzimas presentan una serie de ventajas catalíticas respecto a los catalizadores químicos empleados en síntesis química clásica: especificidad, selectividad y la posibilidad de trabajar en condiciones suaves de temperatura y presión. No obstante, también presentan una serie de limitaciones como son la baja estabilidad y las bajas productividades. En el presente trabajo se combinan dos técnicas para tratar de optimizar las reacciones de interés seleccionadas: la inmovilización y la ingeniería de reacción. Las reacciones objetivo de este trabajo son reacciones de oxidoreducción centradas en la biosíntesis de moléculas, de medio y alto valor añadido, de alto interés industrial. En la primera parte de la tesis se ha utilizado una alcohol deshidrogenasa (ADH99) para la oxidación del alcohol chlorolactol a chlorolactona y una NAD(P)H oxidasa (NOX) como sistema de regeneración del cofactor. La chlorolactona es un precursor para la síntesis de estatinas las cuales son fármacos utilizados para la reducción del LDL-colesterol puesto que inhiben la enzima encargada de su biosíntesis. Ambas enzimas fueron inmovilizados eficientemente en diferentes soportes, de los cuales se seleccionaron los tres que mostraron mayor actividad retenida. Seguidamente se estudió la estabilidad de los derivados inmovilizados en condiciones de reacción y se determinó la carga enzimática máximo para cada enzima. Se descartó el uso de la NOX inmovilizada puesto que no se mejoró la estabilidad con ningún apoyo. Posteriormente se optimizaron las condiciones de reacción con un diseño experimental (DoE) con la ADH99 soluble pero utilizando la cantidad máxima de ADH99 que se puede añadir a la reacción cuando se usa la ADH99 inmovilizada en epoxy-agarosa-UAB M2. Finalmente se estudió la capacidad de reutilización del derivado inmovilizado, donde se pudo mejorar 1.5 veces tanto el producto obtenido como el rendimiento del biocatalizador. No obstante, la mejor configuración resultó ser la utilización de las dos enzimas en forma soluble. La segunda parte de esta tesis se centró en la reacción de oxidación del alcohol vanillínico a vanillina biocatalizada por la eugenol oxidasa (EUGO). La vanillina es la molécula que da las propiedades organolépticas a la vainilla, el segundo aromatizante más caro del mundo. La síntesis de vainillina vía biotecnológica es de un gran interés industrial puesto que puede etiquetarse como natural. La EUGO fue inmovilizada eficientemente en diferentes soportes de los que se seleccionaron los tres que retuvieron más actividad y se estudiaron los mismos parámetros que en el apartado anterior. En este caso los tres derivados inmovilizados fueron utilizados para realizar la reacción de síntesis, con el objetivo de seleccionar el más estable operacionalmente. Todos los derivados permitieron ser reutilizados 5 veces conservando una elevada conversión en el último ciclo. La epoxy-agarosa-UAB M2 fue el soporte que mejor estabilidad mostró. Los buenos resultados obtenidos en el segundo apartado de este trabajo permitieron profundizar en esta reacción. Por lo que, en el tercer apartado, se realizó una optimización de las condiciones de reacción desde el punto de vista de mejorar las métricas del proceso y también con el objetivo de hacer el proceso más sostenible ambientalmente. A la hora de escoger las nuevas condiciones de reacción se tuvieron en cuenta la actividad de la EUGO y su estabilidad. Ambas condiciones fueron testadas en la reacción diana con lo EUGO soluble e inmovilizada. En las nuevas condiciones se pudo mejorar la productividad volumétrica 5.7 y 6.6 veces respectivamente, en comparación a las condiciones previas. Finalmente, en el reciclaje de la enzima inmovilizada se pudieron realizar 5 ciclos de reacción en las primeras condiciones y 18 ciclos de reacción en las nuevas condiciones donde se pudo mejorar el rendimiento del biocatalitzador 3.9 y 12.4 veces respectivamente.
Enzymes have some catalytic advantages over chemical catalysts used in classical chemical synthesis: specificity, selectivity and the possibility to work under mild conditions of temperature and pressure. However, they also have some limitations such as low stability and low productivity. This work combines two techniques aiming to optimise the target reactions: immobilisation and reaction engineering. The target reactions of this work are redox reactions focused on the biosynthesis of molecules, of medium-high value, of industrial interest. In the first part of the thesis, an alcohol dehydrogenase (ADH99) was used, with an NAD(P)H oxidase (NOX) as a cofactor regeneration system, to oxidise a chlorolactol to chlorolactone. Chlorolactone is a precursor for the synthesis of statins which are drugs used to lower LDL-cholesterol by inhibiting the enzyme responsible for its biosynthesis. Both enzymes were efficiently immobilised on different supports, selecting the three that showed the highest retained activity. The stability of the immobilised derivatives under reaction conditions was studied and the maximum enzyme load for each enzyme also was determined. The use of immobilised NOX was discarded because no stability improvements were achieved with any support. The reaction conditions were optimised by design of experiments (DoE), using soluble ADH99 added at maximum loading onto an epoxy-agarose support. Finally, the reusability of the immobilised enzyme was studied, where both the total product obtained and the biocatalyst yield could be improved 1.5-fold. However, the best configuration resulted from the use of the two enzymes in soluble form. The second part of this thesis was focused on the oxidation reaction of vanillyl alcohol to vanillin catalysed by eugenol oxidase (EUGO). Vanillin is the molecule that gives vanilla its organoleptic properties. Vanillin biotechnological synthesis is of high interest industrially because it is the second most expensive flavouring in the world and the product can be labelled as natural. Similar to the previous section, EUGO was efficiently immobilised onto different supports, selecting the three that retained most activity. These supports were used to study the stability of the immobilised enzyme and the maximum EUGO load that can be immobilised. In this case, the three immobilised derivatives were used to perform the target reaction, in order to select the most stable operationally. All immobilised derivatives could be reused 5 times maintaining a high conversion in the last cycle. Epoxy-agarose-UAB M2 was the support that showed the best stability, improving the biocatalyst yield 3-fold. The encouraging results obtained in the second section of this work allowed us to deepen the study of this reaction. Therefore, in the third section, an optimisation of the reaction conditions was carried out to improve the process metrics and also aiming to make the process more environmentally sustainable. The EUGO activity and its stability were taken into account to choose the reaction conditions. Both conditions, maximum activity and maximum stability, were tested in the target reaction with soluble and immobilised EUGO. Using the new conditions, it was possible to improve the volumetric productivity 5.7 and 6.6-fold respectively, compared to the previous conditions. Finally, the reusability of the immobilised EUGO allowed us to perform 5 reaction cycles and 18 reaction cycles, with unoptimised and optimised reaction conditions respectively. This resulted in an improvement of the biocatalyst yield of 3.9 and 12.4-fold, respectively, compared to reactions with soluble enzyme under the same conditions.
Universitat Autònoma de Barcelona. Programa de Doctorat en Biotecnologia
Kasprzak, Jakub [Verfasser]. "Alcohol dehydrogenases as biocatalysts for the production of enantiomerically pure chiral alcohols / Jakub Kasprzak". Greifswald : Universitätsbibliothek Greifswald, 2017. http://d-nb.info/1123167893/34.
Pełny tekst źródłaPalmer, Matthew Jon. "The stereoselective synthesis of alcohols". Thesis, University of Warwick, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263813.
Pełny tekst źródłaKsiążki na temat "Alcohols"
Hall, K. R., i K. N. Marsh, red. Densities of Alcohols. Berlin/Heidelberg: Springer-Verlag, 2000. http://dx.doi.org/10.1007/b75928.
Pełny tekst źródłaMudge, Stephen M. Fatty alcohols: Anthropogenic and natural occurrence in the environment. Cambridge, UK: Royal Society of Chemistry, 2008.
Znajdź pełny tekst źródłaPalmer, Matthew Jon. The stereoselective synthesis of alcohols. [s.l.]: typescript, 1997.
Znajdź pełny tekst źródłaSusette, Khabbaz, i Addiction Research Foundation of Ontario., red. Alcohol concentrations of liquid pharmaceuticals: A compilation of data for products distributed in Canada. Toronto: Addiction Research Foundation, 1990.
Znajdź pełny tekst źródłaOrganization, World Health, red. Lexicon of alcohol and drug terms. Geneva: World Health Organization, 1994.
Znajdź pełny tekst źródłaReeves, R. R., i E. J. Lom. Blending of alcohols with diesel fuels. Vienna, Austria?]: United Nations Industrial Development Organization, 1986.
Znajdź pełny tekst źródłaPoitras, Michael S. Regulation of expression of quinoprotein alcohol dehydrogenase in pseudomonas aeruginosa grown on different alcohols. Sudbury, Ont: Laurentian University, 1996.
Znajdź pełny tekst źródłaDuffield, Melanie Lorraine. Biosynthesis of higher alcohols by brewing yeast. Birmingham: University of Birmingham, 1986.
Znajdź pełny tekst źródłaGribble, Nicholas Robert. Alcohols and other oxygenates in automotive fuels. Birmingham: Aston University. Department of Chemical Engineering, 1987.
Znajdź pełny tekst źródłaMunir, A. Alcohols recovery and purification by azeotropic distillation. Manchester: UMIST, 1997.
Znajdź pełny tekst źródłaCzęści książek na temat "Alcohols"
Clugston, Michael, Malcolm Stewart i Fabrice Birembaut. "Alcohols". W Making the Transition to University Chemistry. Oxford University Press, 2021. http://dx.doi.org/10.1093/hesc/9780198757153.003.0021.
Pełny tekst źródłaZheng, Fuqin, Ziyun Su i Wei Chen. "Graphene-based Nanocomposites for Alcohol Sensing". W Graphene-based Nanocomposite Sensors, 193–221. Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781837671847-00193.
Pełny tekst źródłaPorter, M. J. "Alkanols". W Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00002.
Pełny tekst źródłaPorter, M. J. "Oxidation of Alkanes". W Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00004.
Pełny tekst źródłaPorter, M. J. "Oxidation with Ozone". W Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00006.
Pełny tekst źródłaPorter, M. J. "Oxidation with Dioxiranes". W Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00007.
Pełny tekst źródłaPorter, M. J. "Oxidation with Peroxy Acids". W Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00009.
Pełny tekst źródłaPorter, M. J. "Oxidation with Fluorine". W Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00010.
Pełny tekst źródłaPorter, M. J. "Oxidation with Metal Porphyrins". W Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00011.
Pełny tekst źródłaPorter, M. J. "Oxidation with Ruthenium Compounds". W Alcohols, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00012.
Pełny tekst źródłaStreszczenia konferencji na temat "Alcohols"
Sousa, Gustavo Gomes de, i José Roberto dos Santos Politi. "ASPECTOS ENERGÉTICOS E ELETRÔNICOS DA ZEÓLITA H-ZSM-5 NA AÇÃO CATALÍTICA DA REAÇÃO DE DESIDRATAÇÃO DE ÁLCOOIS". W VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol202087.
Pełny tekst źródłaLi, Xueying, Lei Hou, Chong Chai i Sichen He. "Influence of Alcohol Additives on the Viscosity and Solubility of Ethanol/Diesel Fuel Blends: A Molecular Dynamics Simulation Study". W ASME 2021 Pressure Vessels & Piping Conference. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/pvp2021-61884.
Pełny tekst źródłaZheng, Xuan, Shirin Jouzdani i Benjamin Akih-Kumgeh. "Auto Ignition Study of Methane and Bio Alcohol Fuel Blends". W ASME Turbo Expo 2019: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/gt2019-91978.
Pełny tekst źródłaSugihara, Tatsuya, Takuma Nomura, Toshiyuki Enomoto, Anirudh Udupa, Koushik Viswanathan i James Mann. "Exploring the Role of Mechanochemical Effects in Cutting of Aluminum Alloys With Alcohols". W ASME 2022 17th International Manufacturing Science and Engineering Conference. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/msec2022-85192.
Pełny tekst źródłaPrivat, Romain, Jean-Noël Jaubert i Michel Molière. "Ethanol and Distillate Blends: A Thermodynamic Approach to Miscibility Issues: Part 3 — Generalization to Other Alcohols (Methanol, Isopropanol and 1-Butanol)". W ASME Turbo Expo 2012: Turbine Technical Conference and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/gt2012-68561.
Pełny tekst źródłaLupachev, Egor V., Andrei V. Polkovnichenko i Nikolai N. Kulov. "Purification of organic fluorine alcohols from azeotropic mixtures with non-fluorinated alcohols using extractive distillation". W INTERNATIONAL SCIENTIFIC-TECHNICAL SYMPOSIUM (ISTS) «IMPROVING ENERGY AND RESOURCE-EFFICIENT AND ENVIRONMENTAL SAFETY OF PROCESSES AND DEVICES IN CHEMICAL AND RELATED INDUSTRIES». The Kosygin State University of Russia, 2021. http://dx.doi.org/10.37816/eeste-2021-1-239-241.
Pełny tekst źródłaSingh, P., J. Zhang, A. Ghalgaoui, K. Reimann, B. P. Fingerhut, M. Woerner i T. Elsaesser. "Coherent Underdamped Polarons in Liquid Alcohols". W International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/up.2022.w4a.30.
Pełny tekst źródłaOvchukova, Svetlana, Tatiana Sharonova, Vitaly Likhanov i Oleg Lopatin. "The use of alcohols in transport". W VII INTERNATIONAL CONFERENCE “SAFETY PROBLEMS OF CIVIL ENGINEERING CRITICAL INFRASTRUCTURES” (SPCECI2021). AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0137346.
Pełny tekst źródłaHENRIQUE FREIRE ARAUJO, LUIZ, José Augusto Rosário Rodrigues, FABIO NASARIO i Paulo José Samenho Moran. "Biocatalytic Redox Reactions with Allylic Alcohols". W XXV Congresso de Iniciação Cientifica da Unicamp. Campinas - SP, Brazil: Galoa, 2017. http://dx.doi.org/10.19146/pibic-2017-78725.
Pełny tekst źródłaBerahim, Nor Hafizah, i Akbar Abu Seman. "CO2 Utilization: Converting Waste into Valuable Products". W SPE Asia Pacific Oil & Gas Conference and Exhibition. SPE, 2022. http://dx.doi.org/10.2118/210729-ms.
Pełny tekst źródłaRaporty organizacyjne na temat "Alcohols"
Sentcоv, Valentin, Andrei Reutov i Vyacheslav Kuzmin. Electronic training manual "Acute poisoning with alcohols and alcohol-containing liquids". SIB-Expertise, styczeń 2024. http://dx.doi.org/10.12731/er0778.29012024.
Pełny tekst źródłaAugustine, R. L., i L. K. Doyle. Catalytic oxidation of secondary alcohols. Office of Scientific and Technical Information (OSTI), styczeń 1992. http://dx.doi.org/10.2172/7047071.
Pełny tekst źródłaAugustine, R. L., i L. K. Doyle. Catalytic oxidation of secondary alcohols. Office of Scientific and Technical Information (OSTI), listopad 1992. http://dx.doi.org/10.2172/10187537.
Pełny tekst źródłaDeutsch, M., B. M. Ocko, X. Z. Wu, E. B. Sirota i S. K. Sinha. Surface crystallization in normal-alkanes and alcohols. Office of Scientific and Technical Information (OSTI), czerwiec 1995. http://dx.doi.org/10.2172/80963.
Pełny tekst źródłaKlier, K., R. G. Herman, S. DeTavernier, M. Johannson, M. Kieke i R. D. Bastian. High octane ethers from synthesis gas-derived alcohols. Office of Scientific and Technical Information (OSTI), lipiec 1991. http://dx.doi.org/10.2172/6025861.
Pełny tekst źródłaKlier, K., R. G. Herman, O. C. Feeley i M. A. Johansson. High octane ethers from synthesis gas-derived alcohols. Office of Scientific and Technical Information (OSTI), październik 1992. http://dx.doi.org/10.2172/6873548.
Pełny tekst źródłaKlier, K., R. G. Herman, O. C. Feeley i M. A. Johansson. High octane ethers from synthesis gas-derived alcohols. Office of Scientific and Technical Information (OSTI), lipiec 1992. http://dx.doi.org/10.2172/6557005.
Pełny tekst źródłaKlier, K., R. G. Herman, M. Johansson i O. C. Feeley. High octane ethers from synthesis gas-derived alcohols. Office of Scientific and Technical Information (OSTI), styczeń 1992. http://dx.doi.org/10.2172/5804796.
Pełny tekst źródłaAkgerman, A., i R. G. Anthony. Novel reactor configuration for synthesis gas conversion to alcohols. Office of Scientific and Technical Information (OSTI), styczeń 1990. http://dx.doi.org/10.2172/6404764.
Pełny tekst źródłaAkgerman, A., i R. G. Anthony. Novel reactor configuration for synthesis gas conversion to alcohols. Office of Scientific and Technical Information (OSTI), styczeń 1991. http://dx.doi.org/10.2172/5916190.
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