Relevant bibliographies by topics / Chromatography of aromatic amines

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Chromatography of aromatic amines'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Chromatography of aromatic amines"

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Luceri, Francesca, Giuseppe Pieraccini, Gloriano Moneti, and Piero Dolara. "Primary Aromatic Amines from Side-Stream Cigarette Smoke are Common Contaminants of Indoor Air." Toxicology and Industrial Health 9, no. 3 (1993): 405–13. http://dx.doi.org/10.1177/074823379300900302.

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A very sensitive mass-spectrometry method has been developed for the analysis of aromatic amines in tobacco smoke and in indoor air. Cigarettes were smoked with a smoking machine; the anwies from the smoke were trapped in a 5% HCl water solution containing internal standards and detected by gas chromatography/mass spectrometry in the selected-ion-monitoring (SIM) mode. The amines measured were the following: aniline. 2-toluidine, 3-toluidine, 4-toluidine, 2-ethylaniline, 3-ethylaniline, 4-ethylaniline, 2,3-dimethylaniline, 2,4-dimethylaniline, 2,5-dimethylaniline, 2,6-dimethylaniline, 1-naphth
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Sun, Jian Qi, Ming Tang, and Jun Dai. "Determination of Aromatic Amines in Wastewater by Dispersive Liquid-Liquid Microextraction Coupled to Capillary Gas Chromatography." Advanced Materials Research 881-883 (January 2014): 631–34. http://dx.doi.org/10.4028/www.scientific.net/amr.881-883.631.

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A simple and reliable method combining dispersive liquid-liquid microextracion (DLLME) with gas chromatography (GC) using flame ionization detection (FID) was developed for the simultaneous determination of aniline (AL),o-toluidine (o-TLD),N,N-dimethylaniline (N,N-DAL),p-chloroaniline (p-CAL), andp-nitroaniline (p-NAL) in wastewater. For this purpose, dispersive liquid-liquid microextraction (DLLME) was applied as a sample preparation technique. The DLLME conditions such as the types and volume of extraction solvent, the types and volume of the disperser solvent, pH value and salt addition wer
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D., K. Singh, Singh Shalini, and Srivastava Meenakshi. "Chromatography of aromatic amines on thin layers of zinc ferrocyanide-silica gel G with hybrid CTAB-alcohol-water mobile phase." Journal of Indian Chemical Society Vol. 82, Mar 2005 (2005): 250–53. https://doi.org/10.5281/zenodo.5826999.

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Department of Chemistry. Harcourt Butler Technological Institute, Kanpur-208 002, India E-mail : dhruvksl23@rediffmail.com&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Fax: 91-512-545312 <em>Manuscript received 6 February 2004. revised 9 September 2004. accepted 24 November 2004</em> Thin layer chromatography (TLC) of twenty aromatic amines on zinc ferrocyanide-silica gel G with CTAB or Brij 35-alcohol-water mobile phases has been studied. The effect of surfactant (CTAB) concentration below and above its critical micellar concentration
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Baranitharan, Mathalaimuthu, Barbara Sawicka, and Jayapal Gokulakrishnan. "Phytochemical Profiling and Larval Control of Erythrina variegata Methanol Fraction against Malarial and Filarial Vector." Advances in Preventive Medicine 2019 (April 16, 2019): 1–9. http://dx.doi.org/10.1155/2019/2641959.

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Erythrina variegata (E. variegata) bioactive chemical has been the potential to be utilized as a good, eco-friendly approach for the control of mosquito population. In the present investigation, methanol extract using insecticidal compounds isolated against mosquito larvae kill assay was carried out. Secondary metabolism was characterized by thin layer chromatography, column chromatography, Fourier transform-infrared spectroscopy, gas chromatography-mass spectral, and identification of compound. Mosquito immature third instar larval, Anopheles stephensi, and Culex quinquefasciatus have been ex
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Janda, V., J. Kříž, J. Vejrosta, and K. D. Bartle. "Supercritical fluid extraction and chromatography of aromatic amines." Journal of Chromatography A 669, no. 1-2 (1994): 241–45. http://dx.doi.org/10.1016/0021-9673(94)80354-4.

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Ouyang, Yun-fu, Hai-bo Li, Hong-bing Tang, Yi Jin, and Gui-ying Li. "A reliable and sensitive LCMS-IT-TOF method coupled with accelerated solvent extraction for the identification and quantitation of six typical heterocyclic aromatic amines in cooked meat products." Analytical Methods 7, no. 21 (2015): 9274–80. http://dx.doi.org/10.1039/c5ay01236h.

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Chuang, Gary, Hua-Hsuan Huang, Yu-Feng Chen, and Guang-Hao Niu. "Photoinduced Reduction of Nitrobenzenes to Primary Aromatic Amines." Synlett 28, no. 10 (2017): 1191–94. http://dx.doi.org/10.1055/s-0036-1588953.

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Primary aromatic amines were synthesized from the corresponding nitrobenzenes via photoinduced reduction. The reaction was found to be effective when nitrobenzenes with electron-withdrawing substituents were irradiated with a broad band of UV light centered at 306 nm. When reactions are completed, products could be isolated by acid–base extraction or by column chromatography. This presenting photoreaction procedure for the synthesis of primary aromatic amines from the corresponding nitrobenzenes proceeds without the need of a sensitizer in isopropanol or THF. Without the usage of catalysts, or
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Canales, Romina, Leonardo Mariño-Repizo, Mario Reta, and Soledad Cerutti. "Multi-response optimization of a green solid-phase extraction for the analysis of heterocyclic aromatic amines in environmental samples." Analytical Methods 12, no. 11 (2020): 1504–13. http://dx.doi.org/10.1039/c9ay02712b.

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A method for the multi-response optimization of a green and efficient solid phase extraction treatment combined with liquid chromatography-tandem mass spectrometry was developed for the quantification of ten heterocyclic aromatic amines in waters.
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Dabhi, Ranjitsinh C., Unnati P. Patel, Vaibhavi B. Rathod, Siddharth N. Shah, and Jayesh J. Maru. "Process optimization for acid-amine coupling: a catalytic approach." Current Chemistry Letters 12, no. 1 (2023): 133–40. http://dx.doi.org/10.5267/j.ccl.2022.8.010.

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Proficient routes were devised for coupling different aromatic/aliphatic acids with amines to form amide linkage using various catalysts. Under the optimized reaction conditions, highest conversion was possible without formation of any by-products. All synthesized compounds were purified using column chromatography and characterized by mass spectrometry, nuclear magnetic resonance spectrometry and liquid chromatography-mass spectrometric analysis.
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Torres-Cartas, S., Y. Martín-Biosca, R. M. Villanueva-Camañas, S. Sagrado, and M. J. Medina-Hernández. "Biopartitioning micellar chromatography to predict mutagenicity of aromatic amines." European Journal of Medicinal Chemistry 42, no. 11-12 (2007): 1396–402. http://dx.doi.org/10.1016/j.ejmech.2007.02.022.

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Dissertations / Theses on the topic "Chromatography of aromatic amines"

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Riddar, Jakob B. "Isocyanates, Amines and Alkanolamines : Sampling, Chromatography and Detection." Doctoral thesis, Stockholms universitet, Institutionen för analytisk kemi, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-94067.

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Isocyanates, aromatic-, aliphatic- and alkanolamines are commonly used in the industry today. Millions of workers in Europe are exposed. The most frequent health symptoms are respiratory and dermal disorder. Due to the health risk most of the compounds in this thesis are regulated by authorities and have occupational exposure limits (OELs). Consequently, reliable and robust air sampling methods are urgently needed. In this thesis dry samplers for isocyanates, aliphatic- and alkanolamines have been developed and evaluated. The isocyanate sampler is now a commercial product (ASSET EZ4-NCP Dry Sa
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Lamani-Dixon, Xolelwa [Verfasser], and Torsten Claus [Akademischer Betreuer] Schmidt. "Analysis of aromatic amines in human urine using comprehensive multi-dimensional gas chromatography mass spectrometry / Xolelwa Lamani-Dixon ; Betreuer: Torsten Claus Schmidt." Duisburg, 2018. http://d-nb.info/1173616055/34.

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Marczylo, Timothy Hywel. "Bioactivation of aromatic amines." Thesis, University of Surrey, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336523.

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Walsh, Kelly Ann. "The alkylation of aromatic amines." Thesis, University of Ottawa (Canada), 1992. http://hdl.handle.net/10393/7659.

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N-alkylated anilines can be obtained in moderate yields from aniline and methyl formate in the presence of Rh$\sb6$(CO)$\sb $ and KI after 72 hours at 180-200$\sp\circ$C. Ru$\sb3$(CO)$\sb $ gave similar results to the unpromoted rhodium carbonyl system. Formanilide and N-methylformanilide were also formed in the reaction. The (HCr(CO)$\sb5$) -anion in the form of its PPN$\sp+$ and Et$\sb4$N$\sp+$ salts also catalysed this reaction (under hydrogen) but was selective to the formanilide products. The presence of an electron donating group on the aromatic ring favoured the formation of alkylated p
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Gibson, E. M. "Spectroscopy of jet-cooled aromatic amines." Thesis, Imperial College London, 1988. http://hdl.handle.net/10044/1/47075.

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Wang, Xuan. "Studies on preparation of aromatic amines and their synthetic and biological applications /." View abstract or full-text, 2005. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202005%20WANG.

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Howell, Rachel. "Laser induced fluorescence studies of jet-cooled aromatic amines." Thesis, Imperial College London, 1990. http://hdl.handle.net/10044/1/46347.

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Rohaly, Matthew Joseph. "Decomposition of Aromatic Amines in a Jet Fuel Surrogate." University of Dayton / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1417777531.

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Brunmark, Per. "Methods for assessment of exposure to aromatic amines/isocyanates by air monitoring and biomarkers." Lund : Dept. of Analytical Chemistry and Dept. of Occupational and Environmental Medicine, Lund University, 1994. http://catalog.hathitrust.org/api/volumes/oclc/38948330.html.

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Yeatts, Karin Beatrice. "An investigation of structure activity relationships for aryl nitrenium stability and mutagenicity for amino polyaromatic hydrocarbons." Thesis, This resource online, 1990. http://scholar.lib.vt.edu/theses/available/etd-02132009-170829/.

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Books on the topic "Chromatography of aromatic amines"

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S, Rathore Hamir, ed. Liquid chromatography of polycyclic aromatic hydrocarbons. CRC Press, 1993.

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Organization, World Health, and International Agency for Research on Cancer, eds. Some aromatic amines, organic dyes, and related exposures. IARC Press, 2010.

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Schröder, Stefan. Selektiv O-acylierte Arylhydroxylamine: Herstellung und Reaktionen mit Aminen als Modelle für Schlüsselreaktionen der Carcinogenese aromatischer Amine. A.S. Intemann und C.C. Intemann, 1989.

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Association, Chemical Industries, ed. Safe handling of potentially carcinogenic aromatic amines and nitro compounds. Chemical Industries Association, 1992.

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Maslennikova, I. S. Regulirovanie aminokompleksnymi soedinenii͡a︡mi vlazhnosti dispersnykh ali͡u︡mosilikatnykh sistem. Izd-vo Leningradskogo universiteta, 1985.

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Daszkiewicz, Zdzisław. Aromatyczne nitraminy: Synteza, struktura, właściwości, przegrupowanie. Wydaw. UO, 2004.

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Sin, Han-sŭng. Sikpʻum chung heterocyclic amines monitʻŏring mit wihae pʻyŏngka =: Monitoring and risk analysis for heterocyclic amines in foods. Sikpʻum Ŭiyakpʻum Anjŏnchʻŏng, 2007.

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Ibolya, Molnár-Perl, ed. Quantitation of amino acids and amines by chromatography: Methods and protocols. Elsevier, 2005.

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S, Lee Linda, and National Exposure Research Laboratory (U.S.). Ecosystems Research Division., eds. Modeling soil-water distribution of aromatic amines in water saturated soil systems. U.S. Environmental Protection Agency, Ecosystems Research Division, National Exposure Research Laboratory, 2000.

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S, Lee Linda, and National Exposure Research Laboratory (U.S.). Ecosystems Research Division, eds. Modeling soil-water distribution of aromatic amines in water saturated soil systems. U.S. Environmental Protection Agency, Ecosystems Research Division, National Exposure Research Laboratory, 2000.

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Book chapters on the topic "Chromatography of aromatic amines"

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Alston, Frances, and Onwuka Okorie. "Aromatic amines." In Occupational Exposures. CRC Press, 2023. http://dx.doi.org/10.1201/9781003220114-2.

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Turesky, Robert J. "Aromatic Amines and Heterocyclic Aromatic Amines: From Tobacco Smoke to Food Mutagens." In The Chemical Biology of DNA Damage. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527630110.ch7.

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Turesky, Robert J. "Heterocyclic Aromatic Amines: Potential Human Carcinogens." In Chemical Carcinogenesis. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-61737-995-6_5.

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Davies, A. G. "17.9.6 Radical cations of aromatic amines." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_45.

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Dilworth, J. R., and S. Morton. "From Pyridines and Other Aromatic Amines." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch18.

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Eyer, P. "Activation of aromatic amines by oxyhaemoglobin." In N-Oxidation of Drugs. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3112-4_22.

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Pereira, Luciana, Pijush Kanti Mondal, and Madalena Alves. "Aromatic Amines Sources, Environmental Impact and Remediation." In Pollutants in Buildings, Water and Living Organisms. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-19276-5_7.

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Seigler, David S. "Simple Amines, Simple Aromatic and Pyridine Alkaloids." In Plant Secondary Metabolism. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4913-0_28.

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Krishnamurthy, Naveen Kumar. "Response of Alkaliphilic Bacteria to Aromatic Amines." In Bioprospects of Coastal Eubacteria. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-12910-5_6.

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Mukherjee, Nandini, and Sauvik Chatterjee. "Dehydrogenation Reactions of Aliphatic and Aromatic Amines." In Chemistry of Dehydrogenation Reactions and Its Applications. CRC Press, 2023. http://dx.doi.org/10.1201/9781003321934-6.

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Conference papers on the topic "Chromatography of aromatic amines"

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Nagu, Muthukumar, Saroj K. Panda, and Nayef M. Alanazi. "Organic Amine Partitioning at Simulated Refinery Overhead Condition." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-13225.

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Abstract Organic amines, a neutralizer, are preferentially used over ammonia to minimize the amine hydrochloride induced corrosion in refinery overhead systems. The partition of active ingredients of the neutralizers to the hydrocarbon phase reduces the efficiency of neutralizing amines as the maximum amount of amines are required to be in the aqueous phase to deal with hydrochloric acid present in the system. Moreover, the partitioning of amines to the hydrocarbon phase can form corresponding amine chloride salts leading to the under deposit corrosion in the refinery units. In the present inv
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Pinappu, Sai Reddy, Kwadwo Sarpong, Corina Sandu, and Zhenning Gu. "Fast On-Site Quantification and Monitoring of Monoethanolamine in Crude Oils Using Field Asymmetric Ion Mobility Spectrometry." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05630.

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Abstract Triazine-based hydrogen sulfide (H2S) scavengers are the most commonly used additives in the oil and gas industry. One of the reaction products of the scavenging process is an organic amine. The organic amine by-product, together with amines in slop oil and the desalter wash water, are collectively referred to as “tramp amines.” The most-common tramp amines from the H2S scavenging process are mono-ethanolamine (MEA) and methylamine (MA). These tramp amines have the potential to react with hydrochloric acid (HCl) to form corrosive amine hydrochloride salts in the crude atmospheric dist
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Kouznetsov, D. L., O. Yu Podkopaeva, Yu V. Chizhov, G. P. Antroshenko, S. M. Shevchenko, and A. I. Altsybeeva. "Relationship between the Structure and Activity of Volatile Corrosion Inhibitors Derived from Cyclic Amines." In CORROSION 2001. NACE International, 2001. https://doi.org/10.5006/c2001-01192.

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Abstract Products of the condensation reaction between morpholine or cyclohexylamine and benzaldehydes have been used extensively as volatile inhibitors of atmospheric corrosion, as well as components of lubricant compositions, biocides and preservatives in automotive cooling liquids and fuels. In this study, we examined the relationship between the electronic structure and inhibition performance of the compounds in an atmospheric corrosion test. The condensation products have significantly lower vapor pressure than parent amines, resulting in longer residence times of inhibitor species at a m
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Alghamdi, Talal M. "On-Site Sampling and Determination of Aliphatic Amines in Industrial Waste Water Using Solid Phase Microextraction (SPME)." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-3935.

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Abstract Amine-based corrosion inhibitors are added to the crude oil streams to protect the pipelines from corrosive attacks by oxygen. Amine residuals should be monitored in the system and this is classically done by liquid-liquid extraction (LLE) of amines followed by colorimetric determination using spectrophotometry. Solid phase microextraction (SPME), a novel extraction technique, was used as a sample preparation technique to isolate the amines from the complex sample matrix and gas chromatography (GC) system was used for separation and quantification of amines. A flow-through system was
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Matherly, Ron M., Jian Jiao, David J. Blumer, and Jeffery S. Ryman. "Determination of Imidazoline and Amido-Amine Type Corrosion Inhibitors in Both Crude Oil and Produced Brine from Oilfield Production." In CORROSION 1995. NACE International, 1995. https://doi.org/10.5006/c1995-95543.

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Abstract The classical method for the determination of corrosion inhibitors in oilfield brines is the dye transfer method. Within this method are many variations which the analyst may use to determine the amount of corrosion inhibitor in either water or crude oil. These methods, however, suffer from many interferences which result in both false positive and negatives for corrosion inhibitor content. These methods essentially detect all amines as corrosion inhibitors. Improved high pressure liquid chromatography (HPLC) methods have been developed for the analysis of quaternary salt type corrosi
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Liu, Yaxiong, Xuan Zhang, Zhuoya Luo, Hua Li, and Zhiye Yang. "Rapid Identification of Lingnan Aromatic Traditional Chinese Medicinal Materials Using Deep Learning-Based Headspace-Gas Chromatography-Ion Mobility." In 2024 11th International Conference on Behavioural and Social Computing (BESC). IEEE, 2024. https://doi.org/10.1109/besc64747.2024.10780625.

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Son, Adelina J., and Jayant Chakravarty. "Analysis of Residual Corrosion Inhibitors by Fluorescence and Ultraviolet Spectrophotometry." In CORROSION 1996. NACE International, 1996. https://doi.org/10.5006/c1996-96344.

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Abstract The paper describes the development of a fully automated instrumental procedure for testing residual corrosion inhibitors in production waters in the field. Initial investigations were conducted in the laboratory to evaluate the suitability of ultraviolet and fluorescence spectrophotometric techniques to different types of corrosion inhibitors. Parameters for comparison included selectivity, sensitivity, speed, accuracy and precision of the methods under flowing conditions as in high performance liquid chromatography and static conditions as encountered in stand alone instruments. For
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Soriaga, Manuel P., G. M. Berry, C. Bhardwaj, et al. "Chemisorption of Organic Molecules on Metal Electrode Surfaces." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90300.

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Abstract The chemisorption of various organic functional groups from aqueous solutions onto smooth single-crystal and polycrystalline electrodes, and the resistance of the resulting monolayer intermediates towards electrochemical oxidation have been studied; these investigations were motivated by the need to understand, at the atomic level, metal passivation by monolayer organic coatings. The electrodes employed were Rh, Pd, Ir, Pt, and Au whose anodic dissolution is preceded by surface-oxide formation even in highly acidic media. Resistance towards anodic oxidation can thus be associated with
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Kumar, Dharmendr, Venkata Muralidhar K., Vinay Jain, Beena Rai, and Jeremy Moloney. "Mechanistic Insights into 2-Mercaptoethanol and Thioglycolic Acid Corrosion Inhibitor Chemistries for Mild Steel: DFT and Experimental Investigations." In CONFERENCE 2025. AMPP, 2025. https://doi.org/10.5006/c2025-00518.

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Abstract Sulfur-containing corrosion inhibitors (CIs), such as 2-mercaptoethanol (2ME), thioglycolic acid (TGA), and sodium thiosulfate (STS), are extensively used in oilfield formulations, often in conjunction with other chemistries like quaternary ammonium compounds, imidazolines, and aromatic amines, to mitigate steel corrosion in carbon dioxide environments. These sulfur-based CIs are favored for their effectiveness, low cost, and synergy with other chemistries. To optimize these formulations—by improving performance, reducing costs, and enhancing sustainability—there is a need to better u
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Jackson, Tracey, and Jonathan Vargas. "Selective Loss of Bulk Corrosion Inhibitor Species When Exposed to Glass, Plastic, and Steel." In CORROSION 2020. NACE International, 2020. https://doi.org/10.5006/c2020-14999.

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Abstract Despite the widespread use of corrosion inhibitors (CIs) in the oil and gas industry much of their complex aggregation and adsorption behavior is still very poorly understood. CIs are surface active species meaning that when they are injected into aqueous solutions they naturally aggregate and migrate to gas-liquid, liquid-liquid, and solid-liquid interfaces. A better understanding of each CI component and how it adsorbs when exposed to various surfaces could lead to improved CI design, higher performance at lower dosages, as well as improved methods for residual detection. This paper
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Reports on the topic "Chromatography of aromatic amines"

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Deng, Li. Applications of electrochemically-modulated liquid chromatography (EMLC): Separations of aromatic amino acids and polycyclic aromatic hydrocarbons. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/348887.

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Thomson, J. S., J. B. Green, S. K. T. Yu, and R. P. Vrana. Differentiation of primary, secondary and tertiary aromatic amines in fossil fuels using trifluoroacylation. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/5924565.

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Thomson, J. S., J. B. Green, S. K. T. Yu, and R. P. Vrana. Differentiation of primary, secondary and tertiary aromatic amines in fossil fuels using trifluoroacylation. 1, Analytical methodology. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/10111789.

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Davis, Aika. Polycyclic Aromatic Hydrocarbon Analysis in Propene Smoke Using Thermal Desorption - Gas Chromatography - Mass Spectrometry. National Institute of Standards and Technology, 2024. https://doi.org/10.6028/nist.tn.2321.

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Benkeser, R. Reduction of coal, coal oils and functionalized aromatic compounds derived from coal by calcium in amines: Final report, January 1, 1986--March 31, 1989. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/6137759.

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Bureau of Ocean Energy Management, Alaska OCS Region. Geochemical evaluation, including whole oil gas chromatography, aromatic biomarkers, saturate gcms, isotopes, metals, MSMS, SARA composition and sulfur from an oil sample from the Stinston #1 well. Alaska Division of Geological & Geophysical Surveys, 2018. http://dx.doi.org/10.14509/30120.

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Saturated Gas Chromatography, Saturated Gas Chromatography/Mass Spectrometry 191, 217, 218, and 259 fragmentograms, and Aromatic Gas Chromatography/Total Ion Current and 231 fragmentograms of extracts from the following NPRA well materials: 16 wells listed. Alaska Division of Geological & Geophysical Surveys, 1996. http://dx.doi.org/10.14509/19117.

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Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory : determination of polycyclic aromatic hydrocarbon compounds in sediment by gas chromatography/mass spectrometry. US Geological Survey, 2004. http://dx.doi.org/10.3133/wri034318.

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