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Relevant bibliographies by topics / High performance liquid chromotography

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Academic literature on the topic 'High performance liquid chromotography'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "High performance liquid chromotography"

1

Ducret, A., M. Trani, P. Pepin, and Robert Lortie. "Chiral high performance liquid chromotography resolution of ibuprofen esters." Journal of Pharmaceutical and Biomedical Analysis 16, no. 7 (1998): 1225–31. http://dx.doi.org/10.1016/s0731-7085(97)00212-4.

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SHIN, Hyunsuk, Kenji OGINO, Hisaya SATO, and Eiichi KAWAI. "Separation of Styrene-Methyl Methacrylate-Acrylonitrile Terpolymers by Composition using High Performance Liquid Chromotography." NIPPON GOMU KYOKAISHI 72, no. 12 (1999): 725–30. http://dx.doi.org/10.2324/gomu.72.725.

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Matthaus, Bertrand, Mehmet Musa Özcan, and Fahad Al Juhaimi. "Some rape/canola seed oils: fatty acid composition and tocopherols." Zeitschrift für Naturforschung C 71, no. 3-4 (2016): 73–77. http://dx.doi.org/10.1515/znc-2016-0003.

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Abstract Seed samples of some rape and canola cultivars were analysed for oil content, fatty acid and tocopherol profiles. Gas liquid chromotography and high performance liquid chromotography were used for fatty acid and tocopherol analysis, respectively. The oil contents of rape and canola seeds varied between 30.6% and 48.3% of the dry weight (p<0.05). The oil contents of rapeseeds were found to be high compared with canola seed oils. The main fatty acids in the oils are oleic (56.80–64.92%), linoleic (17.11–20.92%) and palmitic (4.18–5.01%) acids. A few types of tocopherols were found in rape and canola oils in various amounts: α-tocopherol, γ-tocopherol, δ-tocopherol, β-tocopherol and α-tocotrienol. The major tocopherol in the seed oils of rape and canola cultivars were α-tocopherol (13.22–40.01%) and γ-tocopherol (33.64–51.53%) accompanied by α-T3 (0.0–1.34%) and δ-tocopherol (0.25–1.86%) (p<0.05). As a result, the present study shows that oil, fatty acid and tocopherol contents differ significantly among the cultivars.

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Bevilacqua, Paula M., Richard L. Edelson, and Francis P. Gasparro. "High-Performance Liquid Chromotography Analysis of 8-Methoxypsoralen Monoadducts and Crosslinks in Lymphocytes and Keratinocytes." Journal of Investigative Dermatology 97, no. 1 (1991): 151–55. http://dx.doi.org/10.1111/1523-1747.ep12479321.

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Takeuchi, Toyohide, Takeo Niwa, and Daido Ishii. "Precolumn concentration and/or stepwise-gradient elution by switching valve techniques in micro high-performance liquid chromotography." Journal of Chromatography A 407 (January 1987): 141–50. http://dx.doi.org/10.1016/s0021-9673(01)92611-1.

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ANDERSON, J. B., C. E. DAVIS, and J. O. REAGAN. "SIZE EXCLUSION HIGH-PERFORMANCE LIQUID CHROMOTOGRAPHY OF WATER-EXTRACTABLE PROTEINS FROM HOT-PROCESSED, ELECTRICALLY STIMULATED PORK CARCASSES." Journal of Food Quality 11, no. 4 (1988): 303–10. http://dx.doi.org/10.1111/j.1745-4557.1988.tb00890.x.

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Estremera, M. Fabre, J. J. Puente Lanzarote, A. Alonso Llorente, et al. "Comparison of two different methods (turbidimetric inhibition inmunoassay and high performance liquid chromotography) for determination of HbA1c." Clinica Chimica Acta 493 (June 2019): S15. http://dx.doi.org/10.1016/j.cca.2019.03.041.

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You, Jinmao, Yichu Shan, Liang Zhen, Lin Zhang, and Yukui Zhang. "Determination of peptides and amino acids from wool and beer with sensitive fluorescent reagent 2-(9-carbazole)-ethyl chloroformate by reverse phase high-performance liquid chromotography and liquid chromotography mass spectrometry." Analytical Biochemistry 313, no. 1 (2003): 17–27. http://dx.doi.org/10.1016/s0003-2697(02)00398-6.

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Slee, D. J., P. M. Jones, and S. L. Howell. "Proinsulin processing in electrically permeabilized rat islets of Langerhans." Journal of Molecular Endocrinology 5, no. 3 (1990): 275–80. http://dx.doi.org/10.1677/jme.0.0050275.

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ABSTRACT Proinsulin conversion to insulin was studied using electrically permeabilized rat islets of Langerhans. Using high-performance liquid chromotography separation of radiolabelled islet proteins, we have demonstrated that conversion was dependent upon temperature, sensitive to pH and regulated by MgATP. Ammonium acetate was used to collapse the granular pH gradient, over a pH range of 3·5–7·4. Conversion was optimum at pH 4·5–5·5 and was reduced, but not abolished, at pH 7·4. Ca2+ (10 μm) and 4β-phorbol 12-myristate 13-acetate (500 nm), which are insulin secretagogues in permeabilized islets, caused no significant stimulation of conversion.

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Tallarico, Carlo, Silvia Pace, and Antonio Longo. "Quantitation ofL-carnitine, acetyl-L-carnitine, propionyl-L-carnitine and their deuterated analogues by high-performance liquid chromotography tandem mass spectrometry." Rapid Communications in Mass Spectrometry 12, no. 7 (1998): 403–9. http://dx.doi.org/10.1002/(sici)1097-0231(19980415)12:7<403::aid-rcm173>3.0.co;2-n.

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Dissertations / Theses on the topic "High performance liquid chromotography"

1

Li, Zhiguo. "High-performance liquid chromotography analysis of fatty acids and mathematical modeling of liquid chromotography." Ohio University / OhioLINK, 2001. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1179157379.

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Ghugare, Tushar. "Exploring Zirconia as a Column Packing Material." TopSCHOLAR®, 2010. http://digitalcommons.wku.edu/theses/194.

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Zirconia is one of the most promising column packing materials for High Performance Liquid Chromatography (HPLC). The perfect HPLC support material should be energetically homogenous, have a high surface area on which different chemical species can reversibly attach and be physically and chemically stable over a wide range of pH, temperature and solvent conditions. Most existing supports do not have all of these properties. This project is also focused on a proteomics study. Zirconia, hafnium oxide and titanium oxide which are some of the more promising materials currently available, can be used for the separation and analysis of phosphorylated proteins. Adenosine triphosphate, Adenosine diphosphate and Adenosine monophosphate were used as prototypes for phosphorylated proteins. Separation, absorption, fluorescence and SEM studies were performed to determine the adsorption of Adenosine phosphates species at a particular pH on Zirconia. Zirconia was also used for the purification of Fibrinogen Growth Factor (FGF) protein, which are a family of growth factors involved in angiogenesis, wound healing, and embryonic development. The sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) technique was used to analyze the off-column purification and separation of this protein. This research suggests that, at acidic conditions, adenosine monophosphate has more favorable absorption on the Zirconia surface. On the other hand, the separation study suggests that basic conditions are more favorable for the absorption of ATP, ADP and AMP when mixed together on Zirconia 500. Furthermore, it was found that Zirconia is a very promising material for the purification of FGF protein.

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Carpenter, Sarah Elizabeth. "Enzyme linked spectroscopic assays for Glyoxylate the use of Peptidylglycine alpha-Amidating Monoxygenase for the discovery of Novel alpha-Amidated hormones /." [Tampa, Fla] : University of South Florida, 2006. http://purl.fcla.edu/usf/dc/et/SFE0001415.

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Lovell, Christopher Stewart. "High performance bioresorbable liquid crystalline polymers." Thesis, University of Leeds, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.511134.

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Abid, F. M. "High performance liquid chromatography : theory and applications." Thesis, Swansea University, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635837.

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A detailed study was undertaken of both the individual and combined effects of pH, temperature and flow rate on the retention volumes of underivatised amino acids. The relative merits of 3-dimensional S-window diagrams to locate the optimum conditions for the separation of amino acids on a stationary phase comprising 5μ ODS has been successfully performed. The enthalpies of retention of transfer from stationary phase to mobile phase for the amino acids have been measured from the chromatographic data. An isocratic study of the separation of phenylthiohyddation (PTH) amino acids using a 3μ MOS Hypersil reverse phase column was performed by the pre-column derivatisation method. Subsequently, a more detailed investigation was made of the various factors which control the separation, viz. pH, temperature and eluent composition. The conditions for optimum separation were located by constructing, with the aid of a computer, a 3-dimensional S-window diagram. The enthalpy of transfer from stationary phase to mobile phase and the entropy of the process were evaluated from the chromatographic data. A new pre-column derivatisation method for the separation of amino acids by gradient elution was established using an ODS column; this was applied to the analysis of amino acids extracted from mammalian tissue. The retention behaviour of PTH-amino acids was studied on a mixed stationary phase comprising silica bonded to alkylcynanide and octyl silica in the ratio of 60:40, w/w. This factor has an important bearing on the solute retention selectivity of the column. It was found that the selectivity of the acidic and basic PTH-amino acids could be precisely controlled by adjusting the packing percentage and mobile phase composition, suggesting that the mixed phase technique could be profitably exploited for analytical purposes. HPLC group type analyses of oil samples, normally requiring more sophisticated and time consuming methods of analysis, were performed using normal and reverse phase columns of different materials. The separated fraction has been identified by mass spectrometry, and the results obtained have been of some assistance in an investigation relating to poorly combustable oil. Finally, an extended and modified LC theory has been proposed, and a new modified approach which relates the inverse corrected retention volume (1/V<SUB>R</SUB>) and volume fraction composition of polar solvent component (φB) has been established for a polar component variation of 0 to 100% . The results indicate good agreement between the theoretical and experimental values for all systems displaying a non-linear relationship between 1/V<SUB>R</SUB> and φB.

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Norcio, Lawrence P. "Stability studies of coal liquid products using high performance liquid chromatography." Morgantown, W. Va. : [West Virginia University Libraries], 1999. http://etd.wvu.edu/templates/showETD.cfm?recnum=984.

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Thesis (Ph. D.)--West Virginia University, 1999.<br>Title from document title page. Document formatted into pages; contains xi, 152 p. : ill. (some col.) Vita. Includes abstract. Includes bibliographical references (p. 127-133).

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Edwardson, P. A. D. "High Performance Liquid Chromatography of polynucleotides and proteins." Thesis, London School of Hygiene and Tropical Medicine (University of London), 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376534.

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Aggarwal, Pankaj. "High-Performance Polymer Monoliths for Capillary Liquid Chromatography." BYU ScholarsArchive, 2014. https://scholarsarchive.byu.edu/etd/4236.

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This dissertation focuses on improving the chromatographic efficiency of polymeric organic monoliths by characterizing and optimizing the bed morphology. In-situ characterization techniques such as capillary flow porometry (CFP), 3-dimensional scanning electron microscopy (3D SEM) and conductivity measurements were developed and implemented to quantitatively characterize the morphology of poly(ethylene glycol) diacrylate (PEGDA) monoliths. The CFP measurements for monoliths prepared by the same procedure in capillaries with different diameters (i.e., 75, 150, and 250 μm) clearly showed a change in average through-pore size with capillary diameter, thus, certifying the need for in-situ measurement techniques. Serial sectioning and imaging of PEGDA monoliths using 3D SEM gave quantitative information about the average pore size, porosity, radial heterogeneity and tortuosity of the monolith. Chromatographic efficiency was better for a monolith with smaller average pore size (i.e., 5.23 μm), porosity (i.e., 0.49), radial heterogeneity (i.e., 0.20) and tortuosity (i.e., 1.50) compared to another monolith with values of 5.90 μm, 0.59, 0.50 and 2.34, respectively. Other than providing information about monolith morphology, these techniques also aided in identifying factors governing morphological changes, such as capillary diameter, polymerization method, physical/chemical properties of the pre-polymer constituents and weight proportion of the same. A statistical model was developed for optimizing the weight proportion of pre-polymer constituents from their physical/chemical properties for improved chromatographic efficiency. Fabricated PEGDA columns were used for liquid chromatography of small molecules such as phenols, hydroxyl benzoic acids, and alkyl parabens. The chromatographic retention mechanism was determined to be principally reversed-phase (RP) with additional hydrogen bonding between the polar groups of the analytes and the ethylene oxide groups embedded in the monolith structure. The chromatographic efficiency measured for a non-retained compound (uracil) was 186,000 plates/m when corrected for injector dead volume. High resolution gradient separations of selected pharmaceutical compounds and phenylurea herbicides were achieved in less than 18 min. Column preparation was highly reproducible, with relative standard deviation (RSD) values less than 2.1%, based on retention times of the phenol standards (3 different columns). A further improvement in chromatographic performance was achieved for monoliths fabricated using a different polymerization method, i.e., living free-radical polymerization (LFRP). The columns gave an unprecedented column performance of 238, 000 plates/m for a non-retained compound under RP conditions.

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Benson, Andrew James. "High-performance liquid chromatography (HPLC) and high-performance liquid chromatography mass spectrometry (HPLC/MS) for the analysis of date rape drugs." FIU Digital Commons, 2002. http://digitalcommons.fiu.edu/etd/1602.

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The drugs studied in this work have been reportedly used to commit drug-facilitated sexual assault (DFSA), commonly known as "date rape". Detection of the drugs was performed using high-performance liquid chromatography with ultraviolet detection (HPLC/UV) and identified with high performance-liquid chromatography mass spectrometry (HPLC/MS) using selected ion monitoring (SIM). The objective of this study was to develop a single HPLC method for the simultaneous detection, identification and quantitation of these drugs. The following drugs were simultaneously analyzed: Gamma-hydroxybutyrate (GHB), scopolamine, lysergic acid diethylamide, ketamine, flunitrazepam, and diphenhydramine. The results showed increased sensitivity with electrospray (ES) ionization versus atmospheric pressure chemical ionization (APCI) using HPLC/MS. HPLC/ES/MS was approximately six times more sensitive than HPLC/APCI/MS and about fifty times more sensitive than HPLC/UV. A limit of detection (LOD) of 100 ppb was achieved for drug analysis using this method. The average linear regression coefficient of correlation squared (r2) was 0.933 for HPLC/UV and 0.998 for HPLC/ES/MS. The detection limits achieved by this method allowed for the detection of drug dosages used in beverage tampering. This method can be used to screen beverages suspected of drug tampering. The results of this study demonstrated that solid phase microextraction (SPME) did not improve sensitivity as an extraction technique when compared to direct injections of the drug standards.

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Anyakoha, Ngozi G. "Fatty acid and lipid profiles in models of neuroinflammation and mood disorders. Application of high field NMR, gas chromotography and liquid chromotography-tandem mass spectrometry to investigate the effects of atorvaststin in brain and liver lipids and explore brain lipid changes in the FSL model of depression." Thesis, University of Bradford, 2009. http://hdl.handle.net/10454/4328.

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Lipids are important for the structural and physiological functions of neuronal cell membranes. Alterations in their lipid composition may result in membrane dysfunction and subsequent neuronal deficits that characterise various disorders. This study focused on profiling lipids of aged and LPS-treated rat brain and liver tissue with a view to explore the effect of atorvastatin in neuroinflammation, and examining lipid changes in different areas of rat brain of the Flinders Sensitive Line (FSL) rats, a genetic model of depression. Lipids and other analytes extracted from tissue samples were analysed with proton nuclear magnetic resonance spectroscopy (1H-NMR), gas chromatography (GC) and liquid chromatography-tandem mass spectroscopy (LC/ESI-MS/MS). Changes in the lipid profiles suggested that brain and liver responded differently to ageing and LPS-induced neuroinflammation. In the aged animals, n-3 PUFA were reduced in the brain but were increased in the liver. However, following treatment with LPS, these effects were not observed. Nevertheless, in both models, brain concentration of monounsaturated fatty acids was increased while the liver was able to maintain its monounsaturated fatty acid concentration. Atorvastatin reversed the reduction in n-3 PUFA in the aged brain without reducing brain and liver concentration of cholesterol. These findings further highlight alterations in lipid metabolism in agerelated neuroinflammation and show that the anti-inflammatory actions of atorvastatin may include a modulation of fatty acid metabolism. When studying the FSL model, there were differences in the lipid profile of different brain areas of FSL rats compared to Sprague-Dawley controls. In all brain areas, arachidonic acid was increased in the FSL rats. Docosahexaenoic acid and ether lipids were reduced, while cholesterol and sphingolipids were increased in the hypothalamus of the FSL rats. Furthermore, total diacylglycerophospholipids were reduced in the prefrontal cortex and hypothalamus of the FSL rats. These results show differences in the lipid metabolism of the FSL rat brain and may be suggestive of changes occurring in the brain tissue in depression.

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Books on the topic "High performance liquid chromotography"

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Meyer, Veronika. Practical high-performance liquid chromotography. 3rd ed. Wiley, 1998.

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M, Smith Roger. Gas and liquid chromatography in analytical chemistry. Wiley, 1988.

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M, Smith Roger. Gas and liquid chromatography in analytical chemistry. Wiley, 1988.

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Smith, Roger M. Gas and liquid chromatography in analytical chemistry. Wiley, 1988.

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1950-, Stuart Brian, Prichard Elizabeth R, Royal Society of Chemistry (Great Britain), and LGC (Firm), eds. High performance liquid chromatography. Royal Society of Chemistry, 2003.

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(Project), ACOL, ed. High performance liquid chromatography. 2nd ed. Published on behalf of Thames Polytechnic, London, by Wiley, 1992.

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Lindsay, Sandie. High performance liquid chromatography. Edited by Kealey D and ACOL (Project). Published on behalf of ACOL, London by Wiley, 1987.

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Lough, W. J., and I. W. Wainer, eds. High Performance Liquid Chromatography. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-011-0597-2.

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D, Kealey, and ACOL, eds. High performance liquid chromatography. Wiley on behalf of ACOL, 1987.

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Meyer, Veronika. Practical high-performance liquid chromatography. 2nd ed. John Wiley & Sons, 1994.

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Book chapters on the topic "High performance liquid chromotography"

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Talcott, Stephen. "High Performance Liquid Chromatography." In Food Analysis Laboratory Manual. Springer US, 2009. http://dx.doi.org/10.1007/978-1-4419-1463-7_18.

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Reuhs, Bradley L., and Mary Ann Rounds. "High-Performance Liquid Chromatography." In Food Science Texts Series. Springer US, 2010. http://dx.doi.org/10.1007/978-1-4419-1478-1_28.

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Bloch, Michael H., Michael H. Bloch, Mark A. Geyer, et al. "High Performance Liquid Chromatography." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_3304.

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Reuhs, Bradley L. "High-Performance Liquid Chromatography." In Food Science Text Series. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-45776-5_13.

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Nambara, Toshio, and Junichi Goto. "High-Performance Liquid Chromatography." In The Bile Acids: Chemistry, Physiology, and Metabolism. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-0901-7_2.

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Nielsen, S. Suzanne, and Stephen T. Talcott. "High-Performance Liquid Chromatography." In Food Analysis Laboratory Manual. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-44127-6_7.

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Braithwaite, A., and F. J. Smith. "High performance liquid chromatography." In Chromatographic Methods. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-0599-6_6.

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Akash, Muhammad Sajid Hamid, and Kanwal Rehman. "High Performance Liquid Chromatography." In Essentials of Pharmaceutical Analysis. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-15-1547-7_14.

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Talcott, Stephen. "High Performance Liquid Chromatography." In Food Analysis Laboratory Manual. Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-5250-2_17.

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Nielsen, S. Suzanne. "High Performance Liquid Chromatography." In Instructor’s Manual for Food Analysis: Second Edition. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5439-4_32.

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Conference papers on the topic "High performance liquid chromotography"

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Addabbo, Tommaso, Gianluca Bixio, Ada Fort, Marco Mugnaini, Valerio Vignoli, and Francesco Vigni. "High performance liquid chromatography LCC analysis." In 2015 IEEE International Instrumentation and Measurement Technology Conference (I2MTC). IEEE, 2015. http://dx.doi.org/10.1109/i2mtc.2015.7151397.

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RAPP, DOUGLAS. "High energy-density liquid rocket fuel performance." In 26th Joint Propulsion Conference. American Institute of Aeronautics and Astronautics, 1990. http://dx.doi.org/10.2514/6.1990-1968.

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Allen, Paul C., A. D. Barnes, Steven E. Coe, and I. G. Gibb. "High-performance backlights for liquid crystal displays." In SPIE's International Symposium on Optical Engineering and Photonics in Aerospace Sensing, edited by Darrel G. Hopper. SPIE, 1994. http://dx.doi.org/10.1117/12.177806.

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Campidelli, Stephane, Min Jae Kim, Ji Hyun Park, et al. "Graphene: a new liquid crystal for high performance electro-optic applications." In Liquid Crystals XXII, edited by Iam Choon Khoo. SPIE, 2018. http://dx.doi.org/10.1117/12.2501822.

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Clement, Carlos Enrico, and Sung-Yong Park. "High Performance Beam Steering via Tunable Liquid Prisms." In ASME 2016 5th International Conference on Micro/Nanoscale Heat and Mass Transfer. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/mnhmt2016-6580.

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The use of liquids for the manipulation of light has many advantages over their conventional solid counterparts. With the emergence of microfluidic technologies to control fluid interfaces, various devices capable of replacing conventional optical components have been developed. Because liquids are intrinsically smooth and can change shape or form, they have been utilized for highly versatile components to manipulate light with high degrees of control using optofluidic technologies. Liquid lenses and beam steering devices are among the typical optofluidic devices that have gained much interest over recent years. In this work, we present high-performance tunable liquid prisms capable of wide beam steering of incoming light. By using the electrowetting phenomena, we are able to modulate the fluid-fluid interface at which beam steering occurs. Optical analyses were conducted to study the effect of liquid selection in the effectiveness of our prisms. Furthermore, the double-stacked prism configuration is proposed to achieve wide beam steering and its performance is compared with that of a single prism for different liquid selections. Finally, our analytical studies have been experimentally demonstrated. We successfully fabricated the tunable liquid prism filled with water and 1-bromonaphthalene (1-BN). Due to large refractive index difference between two liquids (nwater = 1.33 and n1−BN = 1.65 at λ = 532 nm), high-performance beam steering was enabled. With an apex angle of 25°, we were able to experimentally demonstrate a beam steering of β ≤ 8.82° with the single prism configuration. It was significantly improved up to β ≤ 17.04° for the double-stacked prism.

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Park, I. S., J. W. Yang, S. H. Oh, and S. K. Chung. "Multifuctional liquid lens for high-performance miniature cameras." In 2016 IEEE 29th International Conference on Micro-Electro-Mechanical Systems (MEMS). IEEE, 2016. http://dx.doi.org/10.1109/memsys.2016.7421744.

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Zhou, Ying, Yuhua Huang, and Shin-Tson Wu. "High Performance Dye-Doped Cholesteric Liquid Crystal Lasers." In Organic Photonics and Electronics. OSA, 2006. http://dx.doi.org/10.1364/ope.2006.optub6.

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Lee, Seung Hee. "High performance Fringe-field switching liquid crystal display." In 2011 IEEE Photonics Conference (IPC). IEEE, 2011. http://dx.doi.org/10.1109/pho.2011.6110623.

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Giuliani, Angela, Damiano Giunta, and Alessandro Condini. "Advancing in Liquid Coatings: High Performance Liquid Epoxy Coating for Oil Well Tubing, High Temperature and High Pressure Resistant." In Abu Dhabi International Petroleum Exhibition & Conference. Society of Petroleum Engineers, 2020. http://dx.doi.org/10.2118/202684-ms.

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Chen, Fang, and Song Liu. "Detection of trace nickel in environmental water by high-performance liquid chromatography after dispersive liquid-liquid microextraction." In 2018 7th International Conference on Energy, Environment and Sustainable Development (ICEESD 2018). Atlantis Press, 2018. http://dx.doi.org/10.2991/iceesd-18.2018.325.

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Reports on the topic "High performance liquid chromotography"

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Hood, Patrick J. High-Performance Liquid Crystal Adhesives. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada363644.

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Wu, Shin-Tson. High Performance Liquid Crystals for Laser Communications. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada388296.

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Sales, B. C., L. A. Boatner, B. C. Chakoumakos, J. C. McCallum, J. O. Ramey, and R. A. Zuhr. Structural analysis of amorphous phosphates using high performance liquid chromatography. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10111962.

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Bass, D. A., J. S. Yaeger, J. S. Crain, et al. Arsenic speciation using high performance liquid chromatography-inductively coupled plasma-mass spectrometry. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/102125.

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Han, Chang D. Nanostructured High-Performance Materials Consisting of Bismaleimide and Functional Liquid Crystal Monomer. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada428496.

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Dumont, Philip John. New methods and materials for solid phase extraction and high performance liquid chromatography. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/219499.

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Krikorian, S. E., Trevor A. Chorn, James W. King, and Michael W. Ellzy. Determination of the Partition Coefficients of Organophosphorus Compounds Using High-Performance Liquid Chromatography. Defense Technical Information Center, 1987. http://dx.doi.org/10.21236/ada189276.

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Bass, D. A., J. S. Yaeger, K. J. Parish, et al. Arsenic speciation in soil using high performance liquid chromatography/inductively coupled plasma/mass spectrometry. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/432912.

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Dennis, William E., and Alan B. Rosencrance. Determination of N-Nitroso-N-Ethylurea (ENU) in Salt Water - By High Performance Liquid Chromatography (HPLC). Defense Technical Information Center, 1995. http://dx.doi.org/10.21236/ada297217.

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Freeze, Ronald. Improved resins and novel materials and methods for solid phase extraction and high performance liquid chromatography. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/587891.

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