Academic literature on the topic 'Tartaric acid'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Tartaric acid.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Journal articles on the topic "Tartaric acid"
YAMAMOTO, Yoshikazu. "L(+)-Tartaric acid. d-Tartaric acid." Journal of Synthetic Organic Chemistry, Japan 48, no. 1 (1990): 71–72. http://dx.doi.org/10.5059/yukigoseikyokaishi.48.71.
Full textSpiller, Gene A., Jon A. Story, Emily J. Furumoto, Jo Carol Chezem, and Monica Spiller. "Effect of tartaric acid and dietary fibre from sun-dried raisins on colonic function and on bile acid and volatile fatty acid excretion in healthy adults." British Journal of Nutrition 90, no. 4 (October 2003): 803–7. http://dx.doi.org/10.1079/bjn2003966.
Full textFronczek, Frank R., Richard D. Gandour, Thomas M. Fyles, Philippa J. Hocking, Susan J. McDermid, and P. Daniel Wotton. "Polycarboxylate crown ethers from meso-tartaric acid." Canadian Journal of Chemistry 69, no. 1 (January 1, 1991): 12–19. http://dx.doi.org/10.1139/v91-003.
Full textLosev, Evgeniy, and Elena Boldyreva. "The effect of amino acid backbone length on molecular packing: crystalline tartrates of glycine, β-alanine, γ-aminobutyric acid (GABA) and DL-α-aminobutyric acid (AABA)." Acta Crystallographica Section C Structural Chemistry 74, no. 2 (January 18, 2018): 177–85. http://dx.doi.org/10.1107/s2053229617017909.
Full textHasbullah, Umar Hafidz Asy'ari, Miftahul Wahidatun Ni’mah, Endang Is Retnowati, and Rini Umiyati. "Physical, Chemical, and Sensory Properties of Robusta Coffee Effervescent Tablets Formulated in Various Organic Acids." Pelita Perkebunan (a Coffee and Cocoa Research Journal) 38, no. 1 (April 20, 2022): 54–69. http://dx.doi.org/10.22302/iccri.jur.pelitaperkebunan.v38i1.489.
Full textFukami, Takanori, Shuta Tahara, Chitoshi Yasuda, and Keiko Nakasone. "Structural Refinements and Thermal Properties of L(+)-Tartaric, D(–)-Tartaric, and Monohydrate Racemic Tartaric Acid." International Journal of Chemistry 8, no. 2 (March 10, 2016): 9. http://dx.doi.org/10.5539/ijc.v8n2p9.
Full textSynoradzki, Ludwik, Pawel Ruśkowski, and Urszula Bernaś. "TARTARIC ACID AND ITSO-ACYL DERIVATIVES. PART 1. SYNTHESIS OF TARTARIC ACID ANDO-ACYL TARTARIC ACIDS AND ANHYDRIDES." Organic Preparations and Procedures International 37, no. 1 (February 2005): 37–63. http://dx.doi.org/10.1080/00304940509355401.
Full textJunge, Jonas Yde, Anne Sjoerup Bertelsen, Line Ahm Mielby, Yan Zeng, Yuan-Xia Sun, Derek Victor Byrne, and Ulla Kidmose. "Taste Interactions between Sweetness of Sucrose and Sourness of Citric and Tartaric Acid among Chinese and Danish Consumers." Foods 9, no. 10 (October 9, 2020): 1425. http://dx.doi.org/10.3390/foods9101425.
Full textLuner, Paul E., Aditya D. Patel, and Dale C. Swenson. "(\pm)-Tartaric acid." Acta Crystallographica Section C Crystal Structure Communications 58, no. 6 (May 21, 2002): o333—o335. http://dx.doi.org/10.1107/s0108270102006650.
Full textJung, Yui Jung. "The Influence of Organic Acid on Color Retention after Dyeing - Focusing on succinic acid and tartaric acid." Journal of Health and Beauty 16, no. 2 (August 31, 2022): 163–72. http://dx.doi.org/10.35131/ishb.2022.16.2.163.
Full textDissertations / Theses on the topic "Tartaric acid"
Xie, Wei. "Thermodynamic and structural studies of aqueous chelating agents and their metal complexes at various temperatures and pressures : diethylenetriaminepentaacetic acid (DTPA) and tartaric acid /." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0030/MQ47491.pdf.
Full textMhatre, Bharat Suresh. "Super-enantiospecific Autocatalytic Decomposition of Tartaric Acid and Aspartic Acid on Cu Surfaces." Research Showcase @ CMU, 2013. http://repository.cmu.edu/dissertations/232.
Full textBasaran, Tolga Yener. "Ion Exchangers In The Recovery Of Tartaric Acid From Aqueous Solutions." Master's thesis, METU, 2006. http://etd.lib.metu.edu.tr/upload/12607367/index.pdf.
Full textpKa1, pKa1 <
pH <
pKa2, and pKa2 <
pH for weakly basic resin, and in the pH ranges pH <
pKa1, pKa1 <
pH <
pKa2 for strongly basic resin at each concentration. Results show that the pH of the solution is a more important parameter than the initial concentration that affects the ion exchange equilibrium. Also, Langmuir and Freundlich isotherms were plotted, and it was shown that they were in good agreement with the experimental data especially for the systems that are at low total ion concentrations.
Bakka, Thomas Aleksander. "Synthesis and Mechanistic Studies of Optically Active Tartaric Acid Based Surfactants." Thesis, Norges Teknisk-Naturvitenskaplige Universitet, 2013. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-20995.
Full textLopez, Martinez Marco Antonio. "Studies of tartaric acid modified nickel supported catalysts for enantioselective hydrogenation reactions." Thesis, University of Birmingham, 2011. http://etheses.bham.ac.uk//id/eprint/1491/.
Full textHayes, Monty. "Chiral and racemic calix[6]arenes and their self-assembly /." View online, 2008. http://ecommons.txstate.edu/bchemtad/5.
Full textWade, Charles. "Studies towards the total synthesis of isoavenaciolide and the development of the amino tartrate aldol reaction." Thesis, University of Sheffield, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341816.
Full textJapu, Cristina. "Cyclic derivatives of D-glucose and tartaric acid as building blocks for renewable polyesters." Doctoral thesis, Universitat Politècnica de Catalunya, 2014. http://hdl.handle.net/10803/284660.
Full textEn esta Tesis se han sintetizado mediante reacción de policondensación en masa tres series de copoliesteres aromáticos derivados del poli(etilen tereftalato) (PET), poli(butilen tereftalato) (PBT) y poli(hexametilen tereftalato) (PHT) en los que se han sustituido parcial o totalmente las unidades tereftalicas o las unidades oxialquilénicas por diácidos y dioles cíclicos y bicíclicos obtenidos por derivatización de monómeros de origen natural como son el ácido tartárico y la D-glucosa. También se han sintetizado mediante policondensación en masa y en disolución por vía enzimática una serie de copoliesteres alifáticos derivados del poli(butilen sebacato) en los que las unidades oxibutilénicas y sebácicas se han reemplazado por dioles y diácidos bicíclicos derivados de la D-glucosa. Todas las series se han caracterizado espectroscópicamente mediante FTIR y RMN en disolución. Mediante RMN de 1H se ha determinado la composición de los copolímeros. Por otro lado mediante RMN de 13C se ha estudiado la microestructura de los mismos. Dicho estudio reveló que todos los copolímeros eran al azar. Los pesos moleculares determinados mediante cromatografía de permeabilidad en gel y viscosimetría capilar resultaron ser aceptables, aunque en todos los casos disminuían a medida que aumentaba el contenido del monómero de origen renovable. Las propiedades térmicas se han evaluado mediante calorimetría diferencial de barrido (DSC) y análisis termogravimétrico. Se ha observado que la estabilidad térmica no se ve apenas afectada cuando la sustitución se realiza sobre la unidad oxialquilénica y que por otro lado desciende cuando es la unidad tereftálica la sustituida. Los nuevos copolímeros presentaron temperaturas de transición vítrea superiores, observándose que este aumento era superior en los copolímeros que incorporaban el diol o el diácido bicíclico derivado de la D-glucosa que en los que incorporaban el diol o el diácido monociclico derivado del ácido tartárico. Los copolimeros eran por lo general menos cristalinos, menos cristalizables y con temperaturas de fusión inferiores. La estructura cristalina de los mismos determinada mediante difracción de rayos-X era semejante a la de los homopolimeros PET, PBT y PHT. Se ha estudiado la degradabilidad hidrolitica y la biodegradabilidad de todos ellos mediante medidas de pérdida de peso, pesos moleculares, microscopía electrónica de barrido (SEM), observándose un aumento de ambas propiedades para los nuevos copolímeros.
Morello, Alessandro. "Influence of ph and temperature on metatartaric acid efficiency in white wine tartaric stabilization." Master's thesis, ISA/UL, 2012. http://hdl.handle.net/10400.5/8625.
Full textThe sensitivity of metatartaric acid (MA) to high temperatures is the main limit for its actual use in enology. For this reason MA is generally used only for ready-to-drink wines that are stored for few months in bottle. The objective of this work was to obtain more information about the use of MA in order to prevent tartaric salts precipitation in wine by monitoring its effectiveness along the time. Tartaric stability was followed in a white wine during a ten-week experiment. 10 g/Hl of MA was added to wines with different five pH values, namely 3.0, 3.2, 3.5, 3.7 and 3.9 at room temperature (20°C), and to wines at original pH of 3.2 under three different temperatures commonly found in real storage conditions, precisely 12°C, 20°C and 35°C. To monitor tartaric stability we used a test based on the electrical conductivity developed by Boulton (1983). At the end of the experiment we found both a pH and a temperature effect. It was found a polynomial relation (R2 = 0,85) between tartaric stability and pH. The highest the pH, the highest the instability and the shortest the protection against tartrates precipitation. Furthermore, over 20°C we observed a rapid general decrease of MA effectiveness and that there was a linear relation (R2 = 0,99) between temperature and tartaric stability, so that we can affirm that the highest the temperature, the higher the wine instability; this is probably due to a faster MA hydrolysis. Metatartaric acid is surely able to prevent tartrates precipitation, but since in our experimental conditions it could not protect the wine for longer than one month, we would suggest extreme prudence about its use especially during long storage periods
Guadagnin, Hellen Costerano. "Corrosion resistance study of AA2524 anodized in sulphuric-tartaric acid and sealed with hybrid coatings." Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/3/3137/tde-20072017-152947/.
Full textLigas de alumínio são muito utilizadas na indústria aeronáutica por serem materiais leves e altamente resistentes. Porém, essas ligas são particularmente sensíveis à corrosão localizada em meios que contêm cloretos, e precisam de sistemas robustos de proteção. Uma das metodologias de proteção consiste em anodização. A camada produzida aumenta a resistência à corrosão e também serve como sítio de ancoragem para aplicação de revestimentos orgânicos. A anodização crômica tem sido usualmente empregada na indústria aeronáutica. No entanto, como compostos contendo íons cromato são tóxicos para a saúde e para o meio-ambiente, tratamentos de superfície à base de cromo serão proibidos na indústria espacial em um futuro próximo. Anodização em banho de ácido sulfúrico-tartárico (TSA) é uma alternativa promissora e ambientalmente compatível, a qual já está sendo usada industrialmente com apropriada proteção à corrosão e adesão para pintura. Este estudo tem como objetivo propor um tratamento utilizando um revestimento híbrido sol-gel para melhorar a resistência à corrosão da liga AA2524 anodizada em TSA e que mantenha sua compatibilidade com revestimentos orgânicos. Para isso, camadas anodizadas de alumínio (CAA) foram produzidas em diferentes voltagens e protegidas por camada de híbrido sol-gel obtida pela hidrólise de tetraetilortosilano (TEOS) e glicidóxipropiltrimetóxisilano (GPTMS) em solução com alto teor de água e aplicada pela técnica de dip-coating. A avaliação da resistência à corrosão foi realizada através de espectroscopia de impedância eletroquímica (EIS) em NaCl 0,1 mol.L-1 e por exposição à câmara de névoa salina (norma ASTM B117-11). A morfologia da camada porosa foi investigada por MEV e a espectroscopia de emissão óptica por descarga luminescente (GDOES) foi empregada para avaliar a distribuição do híbrido sol-gel no interior dos poros da camada porosa. As caracterizações por MEV confirmaram que as propriedades da camada (distribuição dos poros, porosidade e espessura) são fortemente dependentes das condições de anodização, e a composição em profundidade obtida por GDOES mostrou que o revestimento híbrido penetrou nos poros da camada anodizada. As duas técnicas de caracterização mostraram uma cobertura ineficiente da camada sol-gel para as amostras anodizadas nas voltagens mais elevadas, provavelmente devido à deposição insuficiente do híbrido. Os testes de EIS com duração de até 1008 h (42 dias) mostraram que, independentemente da voltagem de anodização empregada, a camada anódica coberta com sol-gel ficou estável ocorrendo apenas pequenas evoluções dos diagramas com o tempo de imersão. Além do mais, as amostras protegidas com o revestimento híbrido apresentaram maiores valores de módulo de impedância em baixa frequência do que as amostras anodizadas em TSA e hidrotermicamente seladas (HTsed) usadas como referências. Essa tendência foi confirmada pelo ajuste com circuitos elétricos equivalentes (EEC) dos resultados de EIS que também mostrou que a aplicação do sol-gel híbrido torna mais difícil a penetração do eletrólito agressivo nos poros da camada anodizada quando comparada com as amostras HTSed, e indicou melhor desempenho anticorrosivo para a amostra anodizada em 16 V. Esses resultados foram confirmados pelos testes de névoa salina. A investigação do envelhecimento da solução de sol-gel mostrou pouca mudança na viscosidade da solução de hidrólise em duas semanas de testes e que os revestimentos híbridos aplicados a partir dessas soluções foram estáveis e promoveram boa proteção à corrosão para as amostras anodizadas em TSA, com melhora das propriedades anticorrosivas após 168 h de envelhecimento. Testes preliminares realizados com revestimento orgânico livre de solvente (epóxi) indicaram boa compatibilidade deste com o revestimento híbrido TEOS-GPTMS. O revestimento epóxi propiciou valores de módulo de impedância elevados e estáveis e também boa estabilidade após exposição à câmara de névoa salina quando aplicado sobre o revestimento híbrido aplicado sobre a liga 2524.
Books on the topic "Tartaric acid"
1874-1951, Kenrick Frank B., ed. The application of polarimetry to the estimation of tartaric acid in commercial products. Toronto: [s.n.], 1997.
Find full textGawroński, Jacek. Tartaric and malic acids in synthesis: A source book of building blocks, ligands, auxiliaries, and resolving agents. New York: Wiley, 1999.
Find full textMelnick, Jason Patrick. Conformational study of bis-allylic and mono-allylic compounds by variable temperature nuclear magnetic resonance. 1994.
Find full textParker, Philip M. The 2007 Import and Export Market for Lactic Acid, Tartaric Acid, Citric Acid, and Their Salts and Esters in China. ICON Group International, Inc., 2006.
Find full textParker, Philip M. The 2007 Import and Export Market for Lactic Acid, Tartaric Acid, Citric Acid, and Their Salts and Esters in India. ICON Group International, Inc., 2006.
Find full textThe World Market for Lactic Acid, Tartaric Acid, Citric Acid, and Their Salts and Esters: A 2004 Global Trade Perspective. Icon Group International, Inc., 2005.
Find full textParker, Philip M. The World Market for Lactic Acid, Tartaric Acid, Citric Acid, and Their Salts and Esters: A 2007 Global Trade Perspective. ICON Group International, Inc., 2006.
Find full textParker, Philip M. The 2007 Import and Export Market for Lactic Acid, Tartaric Acid, Citric Acid, and Their Salts and Esters in United States. ICON Group International, Inc., 2006.
Find full textGawroński, Jacek, and Krystyna Gawrońska. Tartaric and Malic Acids in Synthesis: A Source Book of Building Blocks, Ligands, Auxiliaries, and Resolving Agents. Wiley-Interscience, 1999.
Find full textBook chapters on the topic "Tartaric acid"
Bährle-Rapp, Marina. "Tartaric Acid." In Springer Lexikon Kosmetik und Körperpflege, 545. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10337.
Full textGooch, Jan W. "Tartaric Acid." In Encyclopedic Dictionary of Polymers, 730. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_11570.
Full textWinkelmann, Jochen. "Diffusion coefficient of D-tartaric acid into L-tartaric acid and water." In Diffusion in Gases, Liquids and Electrolytes, 3267. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_2639.
Full textHolze, Rudolf. "Ionic conductance of tartaric acid." In Electrochemistry, 500. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_468.
Full textZoecklein, Bruce W., Kenneth C. Fugelsang, Barry H. Gump, and Fred S. Nury. "Tartaric Acid and Its Salts." In Production Wine Analysis, 289–315. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-8146-8_13.
Full textHoffmann, Marcin, and Jacek Rychlewski. "Effects of Solvation for (R,R) Tartaric-Acid Amides." In New Trends in Quantum Systems in Chemistry and Physics, 189–210. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/0-306-46950-2_11.
Full textPardasani, R. T., and P. Pardasani. "Magnetic properties of chromium(III) complex of D(-)tartaric acid." In Magnetic Properties of Paramagnetic Compounds, 213. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_158.
Full textPardasani, R. T., and P. Pardasani. "Magnetic properties of chromium(III) complex of D(-)tartaric acid." In Magnetic Properties of Paramagnetic Compounds, 212. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_157.
Full textPardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear chromium(III) complex with acetylacetone and tartaric acid." In Magnetic Properties of Paramagnetic Compounds, 407–8. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_231.
Full textPardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear chromium(III) complex with acctylacetone and tartaric acid." In Magnetic Properties of Paramagnetic Compounds, 409–10. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_232.
Full textConference papers on the topic "Tartaric acid"
Krug, W. P., and M. Aronson. "Complex Piezoelectric Response of Tartaric Acid Composites." In Sixth IEEE International Symposium on Applications of Ferroelectrics. IEEE, 1986. http://dx.doi.org/10.1109/isaf.1986.201134.
Full textSoltani, A., D. Gebauer, B. Fischer, H. Colfen, and M. Koch. "Monitoring the crystallization of tartaric acid with THz spectroscopy." In 2017 42nd International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz). IEEE, 2017. http://dx.doi.org/10.1109/irmmw-thz.2017.8066993.
Full text"CSA-Based Mortars Manufactured with Tartaric Acid-Based Retarder." In "SP-329: Superplasticizers and Other Chemical Admixtures in Concrete Proceedings Twelfth International Conference, Beijing, China". American Concrete Institute, 2018. http://dx.doi.org/10.14359/51711228.
Full textAlonso, José, Santiago Mata, Elena Alonso, Verónica Díez, and Vanessa Cortijo. "FOUR STRUCTURES OF TARTARIC ACID REVEALED IN THE GAS PHASE." In 72nd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2017. http://dx.doi.org/10.15278/isms.2017.wc05.
Full textPermana, Ahmadi Jaya, Harsasi Setyawati, Hamami, and Irmina Kris Murwani. "The influence of dicarboxylic acids: Oxalic acid and tartaric acid on the compressive strength of glass ionomer cements." In 5TH INTERNATIONAL CONFERENCE AND WORKSHOP ON BASIC AND APPLIED SCIENCES (ICOWOBAS 2015). AIP Publishing LLC, 2016. http://dx.doi.org/10.1063/1.4943317.
Full textCao, Binghua, and Mengbao Fan. "Quantitative analyses of tartaric acid based on terahertz time domain spectroscopy." In 5th International Symposium on Advanced Optical Manufacturing and Testing Technologies, edited by Yudong Zhang, José Sasián, Libin Xiang, and Sandy To. SPIE, 2010. http://dx.doi.org/10.1117/12.864957.
Full textRajesh, K., A. Mani, K. Anandan, K. Gayathri, and A. Arun. "Role of metal and amino acid on the growth and microhardness properties of tartaric acid crystals." In 7TH NATIONAL CONFERENCE ON HIERARCHICALLY STRUCTURED MATERIALS (NCHSM-2019). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5114601.
Full textInomata, Katsuhiko, and Yutaka Ukaji. "Asymmetric 1,3-Dipolar Cycloaddition Utilizing Tartaric Acid Ester as a Chiral Auxiliary." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01796.
Full textG. Babayan, Bella. "Tartaric Acid New Synthetic Derivatives Antibacterial Activity against the Phytopathogenic Pseudomonas syringae." In 2nd International Conference on Advanced Research in Science, Engineering and Technology. Acavent, 2021. http://dx.doi.org/10.33422/2nd.icarset.2021.03.120.
Full textMeng, Fanqing, and Mengkai Lu. "Characterization of linear and nonlinear optical properties of urea-tartaric-acid single crystals." In Photonics China '96, edited by Manfred Eich, Bruce H. T. Chai, and Minhua Jiang. SPIE, 1996. http://dx.doi.org/10.1117/12.252993.
Full text