Academic literature on the topic 'Carboxylic acids'

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Journal articles on the topic "Carboxylic acids"

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Uttry, Alexander, and Manuel van Gemmeren. "Direct C(sp3)–H Activation of Carboxylic Acids." Synthesis 52, no. 04 (2019): 479–88. http://dx.doi.org/10.1055/s-0039-1690720.

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Carboxylic acids are important in a variety of research fields and applications. As a result, substantial efforts have been directed towards the C–H functionalization of such compounds. While the use of the carboxylic acid moiety as a native directing group for C(sp2)–H functionalization reactions is well established, as yet there is no general solution for the C(sp3)–H activation of aliphatic carboxylic acids and most endeavors have instead relied on the introduction of stronger directing groups. Recently however, novel ligands, tools, and strategies have emerged, which enable the use of free
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Lee, Seon Yong, Uijin Jo, Bongsu Chang, and Young Jae Lee. "Effects of Preferential Incorporation of Carboxylic Acids on the Crystal Growth and Physicochemical Properties of Aragonite." Crystals 10, no. 11 (2020): 960. http://dx.doi.org/10.3390/cryst10110960.

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The preferential incorporation of carboxylic acids into aragonite and its effects on the crystal growth and physicochemical properties of aragonite were systematically investigated using a seeded co-precipitation system with different carboxylic acids (citric, malic, acetic, glutamic, and phthalic). Aragonite synthesized in the presence of citric and malic acids showed a remarkable decrease in the crystallinity and size of crystallite, and the retardation of crystal growth distinctively changed the crystal morphology. The contents of citric acid and malic acid in the aragonite samples were 0.6
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Markovic, Zoran, Dalibor Bajduk, and Ivan Gutman. "Geometry and conformation of benzenecarboxylic acids." Journal of the Serbian Chemical Society 69, no. 11 (2004): 877–82. http://dx.doi.org/10.2298/jsc0411877m.

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The geometry, conformations and energy of mono-, di-, and tri-carboxylic derivatives of benzene were studied by means of the AM1 molecular-orbital method. Whereas the species having no carboxylic groups in the ortho-position (benzoic, isophthalic, terephthalic, and trimesic acids) are planar in all their (stable) conformations, those possessing carboxylic groups in the ortho-position (phthalic, 1,2,3-benzenetricarboxylic, and 1,2,4-benzenetricarboxylic acids) assume a non-planar geometry, with one carboxyl group almost orthogonal to the plane of the benzene ring. Various rotamers of each of th
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Cavallaro, Palmira Alessia, Marzia De Santo, Marianna Greco, et al. "Titanium Tetrachloride-Assisted Direct Esterification of Carboxylic Acids." Molecules 29, no. 4 (2024): 777. http://dx.doi.org/10.3390/molecules29040777.

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Ester compounds, widely found in pharmaceutical and natural products, play a crucial role in organic synthesis, prompting the development of numerous methods for their synthesis. An important chemical approach in synthesizing esters from carboxylic acids involves the activation of the carboxyl function, requiring the conversion of the hydroxyl group into a suitable leaving group. This paper presents the findings of our investigations into an efficient method for producing esters from carboxylic acids and alcohols, using the Lewis acid titanium tetrachloride. Titanium tetrachloride has proven h
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Sultanova, R. M., N. S. Khusnutdinova, Yu G. Borisova, et al. "Selective synthesis of some carboxylic acids esters." Журнал общей химии 93, no. 1 (2023): 3–10. http://dx.doi.org/10.31857/s0044460x23010018.

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The synthesis of esters of some carboxylic acids by the method of oxidative esterification was carried out. It was shown that the proposed method allows the selective esterification of carboxylic acids with hindered carboxyl groups. It was found that the synthesized esters have anti-aggregation activity at the level of acetylsalicylic acid.
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Chen, Zhen-Bang, Kui Liu, Fang-Ling Zhang, Qing Yuan, and Yong-Ming Zhu. "Palladium-catalyzed oxidative coupling of arylboronic acid with isocyanide to form aromatic carboxylic acids." Organic & Biomolecular Chemistry 15, no. 38 (2017): 8078–83. http://dx.doi.org/10.1039/c7ob01428g.

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Fujiwara, Takuya, Ryoto Inoue, Takuma Ohtawa, and Makoto Tsunoda. "Liquid-Chromatographic Methods for Carboxylic Acids in Biological Samples." Molecules 25, no. 21 (2020): 4883. http://dx.doi.org/10.3390/molecules25214883.

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Carboxyl-bearing low-molecular-weight compounds such as keto acids, fatty acids, and other organic acids are involved in a myriad of metabolic pathways owing to their high polarity and solubility in biological fluids. Various disease areas such as cancer, myeloid leukemia, heart disease, liver disease, and lifestyle diseases (obesity and diabetes) were found to be related to certain metabolic pathways and changes in the concentrations of the compounds involved in those pathways. Therefore, the quantification of such compounds provides useful information pertaining to diagnosis, pathological co
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van Gemmeren, Manuel, та Alexander Uttry. "The Direct Pd-Catalyzed β-C(sp3)–H Activation of Carboxylic Acids". Synlett 29, № 15 (2018): 1937–43. http://dx.doi.org/10.1055/s-0037-1610150.

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The carboxylic acid moiety is one of the most versatile and abundant functional groups. However, despite of tremendous progress in the field of C–H functionalization reactions its use as a directing group for C(sp3)–H activation has remained limited. In this Synpact article we present the challenges associated with the carboxylic acid moiety as a native directing group and report on the newest developments in this field, including our recent study in which we developed a generally applicable protocol for the direct palladium catalyzed β-C(sp3)–H arylation of propionic acid and related α-branch
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Herges, Rainer, and Wolfgang Reif. "Photoresponsive Carboxylic Acids." Liebigs Annalen 1996, no. 5 (2006): 761–68. http://dx.doi.org/10.1002/jlac.199619960519.

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Abualhasan, Murad N., and David G. Watson. "Tagging Fatty Acids Via Choline Coupling for the Detection of Carboxylic Acid Metabolites in Biological Samples." Current Analytical Chemistry 15, no. 6 (2019): 642–47. http://dx.doi.org/10.2174/1573411014666180516093353.

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Background: Fatty acids and other metabolites containing a carboxyl group are of high interest in biomedicine because of their major role in many metabolic pathways and, particularly in the case of oxidised fatty acids, their high biological activity. Tagging carboxylic acid compounds with a permanent positive charge such as a quaternary ammonium compound could increase the LC-MS detection sensitivity and selectivity. This paper describes a new and novel strategy for analysing carboxylcontaining compounds in biological samples by ESI-MS through coupling to choline. Methods: Coupling of carboxy
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Dissertations / Theses on the topic "Carboxylic acids"

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Shoaf, Glenn Lewis. "Emulsion copolymerization with carboxylic acids." Diss., Georgia Institute of Technology, 1989. http://hdl.handle.net/1853/10255.

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Lynch, Daniel Eric. "Molecular cocrystals of carboxylic acids." Thesis, Queensland University of Technology, 1994.

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Delikatny, Edward James. "NMR studies of carboxylic acids : an investigation of head group behaviour in lyotropic and nematic phases." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26996.

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The orientational order of the methylene segments adjacent to the head group in the lamellar liquid crystalline phase of potassium palmitate/D₂0 was investigated using multinuclear magnetic resonance. Previous studies had shown that the orientational order near the soap--water interface decreased with decreasing temperature, contrary to intuition. To investigate this phenomenon, three isotopically substituted species of palmitic acid were synthesized: palmitic acid-d₃₁, 1-¹³C-2,2-H₂- palmitic acid-d₂₉, and 2,2,3,3-H₄- palmitic acid-d₂₇. These compounds were treated in two complementary fashion
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Das(, dutta) Sima. "Organotin derivatives of hydroxamic acids derived from dibasic carboxylic acid." Thesis, University of North Bengal, 1989. http://hdl.handle.net/123456789/755.

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Nandy, Kajal. "Stable mixed carboxylic acid dimers." Pullman, Wash. : Washington State University, 2009. http://www.dissertations.wsu.edu/Thesis/Summer2009/k_nandy_071409.pdf.

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Thesis (M.S. in chemistry)--Washington State University, August 2009.<br>Title from PDF title page (viewed on Aug. 10, 2009). "Department of Chemistry." Includes bibliographical references (p. 53-55).
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Wiklund, Per. "Synthesis of heterocycles from anthranilic acid and its derivatives /." Stockholm, 2004. http://diss.kib.ki.se/2004/91-7349-913-7/.

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Worrall, Julia. "Asymmetric synthesis of #alpha#-heterosubstituted carboxylic acids." Thesis, University of Sheffield, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242305.

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Morrill, Louis Christian. "Organocatalytic functionalisation of carboxylic acids using isothioureas." Thesis, University of St Andrews, 2014. http://hdl.handle.net/10023/6346.

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This thesis describes investigations into the ability of isothioureas to act as organocatalysts in formal [4+2] cycloadditions between carboxylic acids and various Michael acceptors via C1-ammonium enolate intermediates. Initial research focused upon establishing optimal reaction conditions to affect the asymmetric intermolecular formal [4+2] cycloaddition between a range of arylacetic acids and α-keto-β,γ-unsaturated esters, giving anti-dihydropyranones in high yield (49-87%) and with excellent diastereo- and enantioselectivity (up to 98:2 dr, up to 99% ee). This represented the first time th
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Dalavoy, Tulika Sanjeev. "Electrocatalytic hydrogenation of [alpha]-functionalized carboxylic acids." Diss., Connect to online resource - MSU authorized users, 2006.

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Thesis (Ph. D.)--Michigan State University. Dept. of Chemistry, 2006.<br>Alpha in title represented by the lower case Greek letter. Title from PDF t.p. (viewed on Nov. 20, 2008) Includes bibliographical references (p. 235-245). Also issued in print.
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Bankole, Kehinde Seun. "Uncatalyzed esterification of biomass-derived carboxylic acids." Diss., University of Iowa, 2011. https://ir.uiowa.edu/etd/922.

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To shift from a petroleum-based to a biomass-based economy will require the development not only of biofuels, but also of biorenewable replacements for petroleum-derived chemicals. In this regard, environmentally friendly biomass-derived esters may serve as alternatives to fossil-derived chemicals such as toxic halogenated solvents and glycol ethers. Therefore, esterification of various carboxylic acids that find significant applications in the chemical, pharmaceutical, petrochemical, food, and cosmetic industries has been initiated by the chemical industry. At atmospheric condition, esterific
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Books on the topic "Carboxylic acids"

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Haslam, Edwin. Shikimic acid: Metabolism and metabolites. Wiley, 1993.

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A, Ogliaruso Michael, Patai Saul, and Rappoport Zvi, eds. Synthesis of carboxylic acids, esters, and their derivatives. Wiley, 1991.

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Drayton, C. J. Cumulative index. Thieme, 2008.

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United States International Trade Commission. Sebacic acid from the People's Republic of China. U.S. International Trade Commission, 1993.

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United States International Trade Commission. Sebacic acid from the People's Republic of China. U.S. International Trade Commission, 1994.

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Holder, Alvin A. Dipicolinic acid, its analogues and derivatives: Aspects of their coordination chemistry. Nova Science Publishers, 2011.

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Ogliaruso, Michael A., and James F. Wolfe, eds. Synthesis of Carboxylic Acids, Esters and Their Derivatives (1991). John Wiley & Sons, Inc., 1991. http://dx.doi.org/10.1002/9780470772423.

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Piemonte, Vincenzo. Polylactic acid: Synthesis, properties, and applications. Nova Science Publishers, 2011.

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Segla, Peter. Structures, physico-chemical properties and biological activities of copper (II) pyridinecarboxylates. Nova Science Publishers, 2010.

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Zvi, Rappoport, and Liebman Joel F, eds. The chemistry of hydroxylamines, oximes and hydroxamic acids. Wiley, 2008.

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Book chapters on the topic "Carboxylic acids"

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Woodman, J. S. "Carboxylic Acids." In Coffee. Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-4948-5_8.

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Vollhardt, Peter, and Neil Schore. "Carboxylic Acids." In Organic Chemistry. Macmillan Learning, 2014. http://dx.doi.org/10.1007/978-1-319-19197-9_19.

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Smith, Robert M., and Arthur E. Martell. "Carboxylic Acids." In Critical Stability Constants. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4615-6764-6_12.

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Tucker, William B. "Carboxylic Acids." In Organic Chemistry. CRC Press, 2024. http://dx.doi.org/10.1201/9781003479352-20.

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Thurman, E. M. "Carboxylic Acids and Phenols." In Organic Geochemistry of Natural Waters. Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5095-5_6.

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Colquhoun, H. M., D. J. Thompson, and M. V. Twigg. "Synthesis of Carboxylic Acids." In Carbonylation. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4757-9576-9_6.

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Vančik, Hrvoj. "Derivatives of Carboxylic Acids." In Basic Organic Chemistry for the Life Sciences. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07605-8_8.

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Vančik, Hrvoj. "Derivatives of Carboxylic Acids." In Basic Organic Chemistry for the Life Sciences. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92438-6_8.

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Smith, Robert M., and Arthur E. Martell. "Erratum to: Carboxylic Acids." In Critical Stability Constants. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4615-6764-6_34.

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Collier, S. J., and E. Kataisto. "Carboxylic Acids." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00034.

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Conference papers on the topic "Carboxylic acids"

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Kuklenz, Karl D. "Degradation of Carboxylic Acids and the Associated Impact on Feed Prep and Overhead Corrosion." In CORROSION 2017. NACE International, 2017. https://doi.org/10.5006/c2017-09289.

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Abstract This paper describes the thermal and/or hydrolytic stability behavior of solutions of carboxylic acids commonly used in refinery feed prep units and characterizes their daughter molecules. Crude oils are often treated with carboxylic acids to help accomplish some of the goals of refining feed prep units such as pH adjustment, amine removal, and metals removal. These acids, like the crude oil, are subjected to the extreme temperatures of the crude furnace when they pass the desalter dissolved in the crude oil or as unresolved water carryover. Often, the thermal decomposition values for
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Kingston, W. R. "Temporary Corrosion Inhibiting Systems for Ferrous and Non-Ferrous Metals." In CORROSION 2001. NACE International, 2001. https://doi.org/10.5006/c2001-01440.

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Abstract Temporary corrosion inhibiting coatings are applied to metal articles for protection during manufacture, transportation or storage. Various sulfonates or carboxylic acids are often used in such corrosion inhibiting coatings. Combinations of sulfonates and carboxylic acids are generally more effective than the same level of either alone.1 This effect is demonstrated for calcium and sodium dinonylnaphthalene sulfonate with a succinic acid derivative and an oxidized petrolatum. Calcium, magnesium, sodium and ammonia salts of dinonylnaphthalene sulfonic acid are combined with a succinic a
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Wyman, Donald P. "In Pursuit of Non-Phosphorous Corrosion Inhibitors for Cold Water Cooling Systems." In CORROSION 1998. NACE International, 1998. https://doi.org/10.5006/c1998-98217.

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Abstract An exploratory program was conducted to evaluate a number of polymers and carboxylic acid combinations with polymers as non-phosphorus containing, all organic corrosion inhibitors for cold water systems such as evaporative towers. The concentrations of treatment were approximately those which would obtain for current commercial formulations. There was a strong dependency of performance on the "aggressiveness" of the water, especially the conductivity. The polymers were adequate for non-aggressive waters, and one, polymaleic acid (as the sodium salt) performed reasonably in somewhat mo
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Kahyarian, Aria, Bruce Brown, and Srdjan Nesic. "CO2 Corrosion, H2S Corrosion, Organic Acid Corrosion - a Unifying Perspective on Corrosion Mechanisms in Weak Acid Solutions." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-12876.

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Abstract Recent developments in understanding the mechanism of mild steel corrosion in the presence of carboxylic acids, carbon dioxide, and hydrogen sulfide has challenged the conventional views to corrosion in anoxic environments. Conventionally, the high corrosivity of such environments was associated with the direct reduction of these weak acids. Within the last few years, experimental and theoretical investigations of the electrochemical behavior of these corrosive environments suggest that the buffering effect arising from the dissociation of weak acids at the vicinity of metal surface i
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Kahyarian, Aria, Bruce Brown, and Srdjan Nesic. "Fundamental Mechanisms of Mild Steel Corrosion in H2S Containing Environments." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-12875.

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Abstract The current understanding of the corrosion mechanisms in H2S containing environments is based on the direct electrochemical reduction of H2S as the main contribution of this species to the corrosion process. Such an argument has been developed based on the distinctive behavior of cathodic polarization curves in H2S containing solutions, as compared to the behavior observed in the solutions of strong acids or those in presence of other weak acids such as carboxylic acids and carbonic acid. The direct reduction of H2S is generally associated with the observation of a “double wave” in a
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Dias, O. C., and M. C. Bromel. "Case History of Microbially Induced Organic Acid Underdeposit Attack in a Gas Pipeline." In CORROSION 1989. NACE International, 1989. https://doi.org/10.5006/c1989-89194.

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Abstract A detailed investigation was conducted into a leaking undersea carbon steel gas pipeline. Attack was confined to low areas where water had accumulated. Metallurgical, biological and chemical analyses showed that pitting, which occurred under deposits, was caused by organic acids generated by bacteria. We have concluded that the metabolic activities of anaerobic sporeformers (Clostridia and Butyribacteria) produced these acids. The pitting mechanism is defined and illustrated. Laboratory biocide testing showed both alkyl amine carboxylic acid and metronidizole to be very effective at l
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Pujar, Mohan, Albert E. Miller, Kunigahalli L. Vasanth, and Gautam Banerjee. "Some Investigations on the Monocarboxylic Acid Based Inhibitors for Aluminum Alloys." In CORROSION 2000. NACE International, 2000. https://doi.org/10.5006/c2000-00331.

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Abstract This paper deals with the electrochemical investigations on three (Capric, Lauric and Myristic acids) different long chain carboxylic acids as inhibitors that were studied in a solution of water and an alcohol at pH of 8.4 - 8.5. The Electrochemical Impedance Spectroscopic (EIS) and potentiodynamic anodic polarization experiments were conducted on Al 2024 and Al 6061 specimens in the solutions containing these inhibitors to determine the effectiveness of these inhibitors. Among the three acids, Lauric acid was found to be the most effective in inhibiting the uniform and localized corr
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Mayer, Bernd, Wolfgang Hater, and Matthias Schweinsberg. "Environmentally Sound Corrosion Inhibitors for Cooling Water." In CORROSION 1999. NACE International, 1999. https://doi.org/10.5006/c1999-99105.

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Abstract Standard corrosion inhibitors for cooling water are based either on heavy metals, phosphates or phosphonates and therefore contribute to the contamination of surface water with noxious substances. Evaluations in pilot plants suggest that phosphorous-free organic carboxylic acids might be promising alternatives to the well-established phosphonic acids. The carboxylic compounds are biodegradable and therefore environmentally favorable. Moreover, in order to accelerate the evaluation of new inhibitors, an electrochemical test has been implemented which operates under conditions close to
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Cragnolino, G., and T. Christman. "Effect of Organic Acids on the IGSCC of Sensitized AISI 304 Stainless Steel in High Temperature Aqueous Solutions." In CORROSION 1986. NACE International, 1986. https://doi.org/10.5006/c1986-86247.

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Abstract The effect of low molecular weight carboxylic acids on the IGSCC of sensitized AISI 304 SS in high temperature (275°C) water was investigated using slow strain rate tests. Significant differences were found by comparing the effect of formic, acetic, and oxalic acids at a concentration of 4.35×10−4M over a wide range of oxygen contents (0.005 to 8.0 ppm). At intermediate dissolved oxygen concentrations (0.2 and 0.6 ppm) formic and oxalic acids suppressed IGSCC, whereas acetic acid accelerated it. The IGSCC behavior was correlated with the corrosion potential of the alloy. The presence
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Keiser, James R., Michael P. Brady, Jeffrey K. Thomson, Raynella M. Connatser, Samuel A. Lewis, and Donovan N. Leonard. "Bio-Oil Properties and Effects on Containment Materials." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-4423.

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Abstract Biomass derived liquids offer a potential for conversion into liquid fuels such as gasoline, jet fuel, diesel, and fuel oil. However, the bio-oils, whether produced by any of a number of processes, contain significant concentrations of water and oxygen-containing organic compounds. Of the oxygenates, carboxylic acids constitute a significant fraction, and these compounds, primarily formic and acetic acids, make bio-oil quite acidic. Unless the carboxylic acids are removed, bio-oil presents corrosion issues for materials used to construct the systems used for production, processing, tr
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Reports on the topic "Carboxylic acids"

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Bastos de Sousa, Fabiula Danielli, and Matheus Alves Rodrigues. Polymeric blends containing different carboxylic acids. Universidad de los Andes, 2024. https://doi.org/10.51573/andes.pps39.ss.cep.4.

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A single-screw extruder was used to produce polymeric blends comprising recycled high-density polyethylene (HDPE) and thermoplastic starch (TPS). Carboxylic acids with varying lengths of carbon chains were used as compatibilizing agents in the blends. While the mechanical properties did not show significant differences among the blends containing com patibilizing agents, all exhibited superior results compared to those without a compatibilizing agent. Therefore, opting for the more cost-effective acid is advisable
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Tamada, Janet, and C. King. Extraction of carboxylic acids by amine extractants. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/6479901.

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Ruangpornvisuti, Vithaya. A study of protonation and deprotonation of the novel amino acids : the compounds of aspartic acids : research repor. Chulalongkorn University, 1997. https://doi.org/10.58837/chula.res.1997.16.

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Acidity and basicity constants of N-acetylaspartic acid, aspartic acid, aspartylaspartic acid, Asp-Asp-Asp, Asp-Asp-Asp-Asp, Asp-Asp-Asp-Asp-Asp and Asp-Asp-asp-Asp-Asp-Asp were determined in 0.1 M potassium nitrate at 25 degree celsius, by means of potentiometric titration. Acidity constants of N-acetylaspartic acid are log K1 = -3.41 and log K2 = -5.13. Basicity constants, expressed as log K, of aspartic acid (asp) and polyaspartic acids (asp)n ; when n=2 to 6, are 9.80 and 8.79, 8.34, 8.50, 8.56 and 8.99 respectively. The number of acidity constant of polyaspartic acids (asp)n is equal to n
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Poole, Loree Joanne, and C. Judson King. Novel Regenerated Solvent Extraction Processes for the Recovery of Carboxylic Acids or Ammonia from Aqueous Solutions Part I. Regeneration of Amine-Carboxylic Acid Extracts. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/937438.

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Peterman, Dean R., Gregory P. Horne, Jamie M. Gleason, Anneka J. Miller, and Stephen P. Mezyk. Determine rate of reaction of hydroxyl radical with carboxylic acids and polyaminocarboxylates. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1483694.

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Tung, Lisa A. Recovery of carboxylic acids at pH greater than pKa. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10125672.

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Starr, John N. Water-enhanced solubility of carboxylic acids in organic solvents and its applications to extraction processes. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/10146497.

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Starr, J. N., and C. J. King. Water-enhanced solubility of carboxylic acids in organic solvents and its applications to extraction processes. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/5273252.

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Eskay, T. P., P. F. Britt, and A. C. III Buchanan. Pyrolysis of simple coal model compounds containing aromatic carboxylic acids: Does decarboxylation lead to cross-linking? Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/197833.

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Burton, Patrick D., and Matthew Tezak. Variable Chain Length Carboxylic Acids as Modifiers to Enhance the Antiviral Efficacy of Sodium Dodecyl Sulfate. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1634888.

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