Relevant bibliographies by topics / Hydrophobic compounds

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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 'Hydrophobic compounds'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Hydrophobic compounds"

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Barnoud, Jonathan, Giulia Rossi, Siewert J. Marrink, and Luca Monticelli. "Hydrophobic Compounds Reshape Membrane Domains." PLoS Computational Biology 10, no. 10 (October 9, 2014): e1003873. http://dx.doi.org/10.1371/journal.pcbi.1003873.

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Schwarzenbach, R. P., and J. Westall. "Sorption of Hydrophobic Trace Organic Compounds in Groundwater Systems." Water Science and Technology 17, no. 9 (September 1, 1985): 39–55. http://dx.doi.org/10.2166/wst.1985.0081.

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Factors influencing the subsurface sorption behavior of neutral and ionizable trace organic compounds are discussed. At equilibrium, the sorption of a neutral hydrophobic organic compound can be expressed by a simple partition coefficient. Partition coefficients, and thus retardation factors, may be estimated from the octanol/water partition coefficient of the compound and the organic carbon content of the aquifer material, if the organic carbon content exceeds 0.1%. For ionizable (anionic) hydrophobic compounds (represented by chlorinated phenols), the distribution ratio depends on both the pH and ionic strength of the aqueous phase, in contrast to the partitioning model for neutral compounds in which the composition of the aqueous phase is relatively unimportant.
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Ahuja, Eric S., and Joe P. Foley. "Separation of very hydrophobic compounds by hydrophobic interaction electrokinetic chromatography." Journal of Chromatography A 680, no. 1 (September 1994): 73–83. http://dx.doi.org/10.1016/0021-9673(94)80054-5.

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Rybarczyk, Piotr, Bartosz Szulczyński, and Jacek Gębicki. "Simultaneous Removal of Hexane and Ethanol from Air in a Biotrickling Filter—Process Performance and Monitoring Using Electronic Nose." Sustainability 12, no. 1 (January 3, 2020): 387. http://dx.doi.org/10.3390/su12010387.

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Biofiltration is a well-accepted method for the removal of malodorous compounds from air streams. Interestingly, the mechanisms underlying this process are not fully understood. The aim of this paper was to investigate the simultaneous removal of hydrophobic hexane with hydrophilic ethanol, resulting in the enhanced removal of hexane in the presence of ethanol. Investigations were performed in a peat-perlite packed biotrickling filter and the process performance was monitored using both gas chromatography and electronic nose techniques. The results indicate that the length as well as the efficiency of biofiltration during the start-up period depend on the feed composition, with higher efficiency obtained when hexane and ethanol were fed together from the process initiation. The experiments in the steady-state period present the biofilter performance when different ratios of hydrophilic to hydrophobic compounds were fed to the biofilter. The obtained results show the synergistic effects of the addition of a hydrophilic compound on the removal efficiency of hydrophobic hexane. The influence of the ratio of hydrophilic to hydrophobic compounds is discussed in terms of enhancing the mass transfer phenomena for hydrophobic volatile organic compounds.
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Tabushi, Iwao, Tatsuya Nabeshima, Kazuo Yamamura, and Mikio Tsuda. "Artificial receptor recognizing hydrophobic carbonyl compounds." Journal of Organic Chemistry 51, no. 10 (May 1986): 1918–21. http://dx.doi.org/10.1021/jo00360a056.

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Morgan, Meredith T., Michael A. Carnahan, Chad E. Immoos, Anthony A. Ribeiro, Stella Finkelstein, Stephen J. Lee, and Mark W. Grinstaff. "Dendritic Molecular Capsules for Hydrophobic Compounds." Journal of the American Chemical Society 125, no. 50 (December 2003): 15485–89. http://dx.doi.org/10.1021/ja0347383.

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Shimizu, Y., H. Sogabe, and Y. Terashima. "The effects of colloidal humic substances on the movement of non-ionic hydrophobic organic contaminants in groundwater." Water Science and Technology 38, no. 7 (October 1, 1998): 159–67. http://dx.doi.org/10.2166/wst.1998.0289.

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A controlled experimental study of the sorption of colloidal humic substances (humic acid) and a non-ionic hydrophobic organic compound (naphthalene) onto typical inorganic constituents of aquifer solids was performed using four types of model solid phases {i.e., individual model solids (montmorillonite, kaolinite, amorphous aluminosilicate gel, and amorphous iron oxides) and combined model solids (montmorillonite coated by amorphous aluminosilicate gel or iron oxides)}, which are synthesized in the laboratory. The batch experimental results indicated that the sorption of non-ionic hydrophobic organic compounds and colloidal humic substances onto the aquifer solids is significantly influenced by the solid composition. And it was also suggested that the non-ionic hydrophobic organic compounds which have greater hydrophobicity are considered to be sorbed and stabilized by the mobile colloidal humic substances in groundwater, and these colloids may act as a third phase that can increase the amount of compounds that the flow of groundwater can transport. On the other hand, the non-ionic hydrophobic organic contaminants of smaller hydrophobicity may be retarded significantly with the sorption of colloidal humic substances onto the aquifer solids.
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Akiba, Isamu, Ryosuke Nakanishi, Masaki Kugimoto, Daisuke Kugimoto, Yusuke Sanada, and Kazuo Sakurai. "ASAXS Study on Spatial Distribution of Hydrophobic Compounds in Polymer Micelles." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1580. http://dx.doi.org/10.1107/s2053273314084198.

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In drug delivery system (DDS) using polymer micelles as drug carrier, DDS properties are related to spatial distribution of drug compounds in the micelles [1]. Because the spatial distribution of drug compounds should strongly depend on interactions and solubility of drug compounds in the micelles, elucidation of the relation between chemical structures of drug compounds and their spatial distribution in the micelle is much important. Thus, in this study, we examine to elucidate the relation between chemical features and spatial distribution of drug compounds in polymer micelles by using anomalous small-angle X-ray scattering (ASAXS). To apply the ASAXS near bromine K-edge for analysis [2] of spatial distribution of drug compounds in polymer micelles, we employ 4 different bromine-labeled hydrophobic compounds as model drug compounds and polymer micelles composed of poly(dimethylaminoethyl methacrylate)-block-poly(methyl methacrylate) (PDMAEMA-b-PMMA). Figure shows SAXS and resonant term obtained from ASAXS near bromine K-edge for the polymer micelles containing 9-bromofluorene (BrF). The domain size estimated from the resonant term is much smaller than that of hydrophobic PMMA core of the micelle. Therefore, When BrF, which is highly hydrophobic and scarcely dissolved in hydrophobic PMMA, is incorporated in the polymer micelle, BrF forms small droplet in the hydrophobic core composed of PMMA. For the micelles incorporating bromobenzene, which as similar properties of BrF, similar result is obtained. On the other hand, 4-bromobenzyl alcohol and ethyl 2-bromoethyl propionate, which are miscible with PMMA, are homogeneously dispersed in the PMMA core of the micelles. These results indicate that highly hydrophobic compounds forms small droplet in hydrophobic core, and introduction of polarity to the compounds causes expansion of the area existing the hydrophobic compounds in polymer micelle.
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Wang, Sin-Jie, Hsiao-Ting Lu, Yu-Chao Wang, Hsin-Ying Huang, and Chung-Shi Yang. "A rapid screening method to select microdialysis carriers for hydrophobic compounds." PLOS ONE 16, no. 9 (September 1, 2021): e0256920. http://dx.doi.org/10.1371/journal.pone.0256920.

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Microdialysis is a minimally invasive sampling technique which is widely applied in many fields including clinical studies. This technique usually has limitation on sampling hydrophobic compounds as aqueous solutions are commonly used as the perfusates. The relative recovery of hydrophobic compounds is often low and irreproducible because of the non-specific binding to microdialysis membranes or catheter tubing. Carriers such as cyclodextrins have been used to improve the recovery and consistency, however the identification of an optimal carrier can only be achieved after time-consuming and costly microdialysis experiments. We therefore developed a rapid, convenient, and low-cost method to identify the optimal carriers for sampling hydrophobic compounds with the use of centrifugal ultrafiltration. Doxorubicin was used as the model compound and its relative recoveries obtained from centrifugal ultrafiltration and from microdialysis were compared. The results show that the relative recoveries are highly correlated (correlation coefficient ≥ 0.9) between centrifugal ultrafiltration and microdialysis when different types or different concentrations of cyclodextrins were used as the carriers. In addition to doxorubicin, this method was further confirmed on three other drugs with different hydrophobicity. This method may facilitate and broaden the use of microdialysis perfusion on sampling or delivering hydrophobic substances in various applications.
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Voronkova, Y. S., and N. I. Shtemenko. "Вплив кластерних сполук ренію з органічними лігандами на активність глюкозооксидази." Visnyk of Dnipropetrovsk University. Biology, medicine 2, no. 1 (March 21, 2011): 18–23. http://dx.doi.org/10.15421/021103.

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Influence of cluster rhenium compounds with different ligands on the activity of glucoseoxidase was studied. Ability of the rhenium compounds to influence on the enzyme’s activity was ascertained. Itis depended on the compound structure and the time of incubation: activity of the glucoseoxidase changed by 4–24 %. The cluster compound with GABA ligand reduced the enzymatic activity, but compounds with hydrophobic ligands increased the activity of glucoseoxidase. Different mechanisms of the cluster rhenium compound–enzyme interactions are suspected.
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Dissertations / Theses on the topic "Hydrophobic compounds"

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Szecsödy, James Edward. "Sorption Kinetics of Hydrophobic Organic Compounds onto Organic Modified Surfaces." Diss., The University of Arizona, 1988. http://hdl.handle.net/10150/219433.

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The sorption of five chlorinated benzenes and sixteen other organic solutes was investigated by determining the extent of sorption and the sorption rates in a series of 40 batch and 139 column experiments using surface-modified silica of known chemical composition. These surfaces were used to represent important functional groups in soil, and consisted of porous silica with patchy surface coatings of aliphatic chains (C₁, C₈, and C₁₈), and other substituent groups (phenyl, amine, alcoholic, and carboxylic). Three possible rate-limiting steps were examined: diffusion through immobile pore fluid, diffusion through bound organic matter, and the chemical binding and release rate. First-order desorption rate coefficients were observed to be 10⁻¹ to 10⁻² s⁻¹ on unbonded, and C₈, C₁₈, amine, and alcoholic modified surfaces, and 10⁻³ to 10⁻⁵ s⁻¹ on C₁ and phenyl-polymer modified surfaces. Diffusion through immobile pore fluid had only a minor effect on the sorption rate, as evidenced by similar rates on organic-bound porous and solid particles. The diffusion rate through the bound organic layer is not rate limiting due to the small organic layer thickness. The observed slow desorption on the phenyl-polymer surface is consistent with the rate limiting step being the chemical binding and release rate. The changes in the rate with temperature and within a series of chlorinated benzenes support this conclusion. The free energies for sorption onto the phenyl-polymer surface ranged from -4.0 kcal mol⁻¹ for chlorobenzene to -6.9 kcal mol⁻¹ for pentachlorobenzene, which are within the range expected for van der Waals interactions. The observed sorption energies are slightly stronger than predicted for hydrophobic surfaces, possibly reflecting strong binding due to multiple pi-pi electron interactions on the phenyl-polymer surface. Hydrophobic solute partitioning onto natural soils, as observed by others, is less than that observed on aliphatic and phenyl hydrophobic surfaces in this study, but greater than on amine or alcoholic modified surfaces. The sorption of di-, tri-, and tetra-chlorobenzenes onto the phenyl-polymer surface is apparently driven by the overall sorption enthalpy (ΔH° = -3.9 to -4.9 kcal mo1⁻¹) and to a lesser extent by the entropy (TΔS° = 0.5 to 1.5 kcal mol⁻¹). As equilibrium of the reactions observed in this study are reached within hours, these reactions are important at small field scales where residence times are hundreds of hours or less.
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Wu, Shian-chee. "Transport of hydrophobic organic compounds between water and natural sediments." Thesis, Massachusetts Institute of Technology, 1986. http://hdl.handle.net/1721.1/15099.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Civil Engineering, 1986.
MICROFICHE COPY AVAILABLE IN ARCHIVES AND ENGINEERING.
Bibliography: leaves 159-168.
by Shian-chee Wu.
Ph.D.
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Morris, Kenneth Robert 1951. "THE SOLUBILITY OF HYDROPHOBIC POLLUTANTS IN WATER-COSOLVENT MIXTURES." Thesis, The University of Arizona, 1986. http://hdl.handle.net/10150/276659.

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Bruant, Robert Gilbert. "Adsorption of volatile hydrophobic organic compounds at the vapor/water interface." Diss., The University of Arizona, 2000. http://etd.library.arizona.edu/etd/GetFileServlet?file=file:///data1/pdf/etd/azu_e9791_2000_292_sip1_w.pdf&type=application/pdf.

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Mohseni, Tonekaboni Madjid. "Biofiltration of hydrophilic and hydrophobic volatile organic compounds using wood-based media." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape17/PQDD_0014/NQ35255.pdf.

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Badea, Silviu-Laurentiu. "Association of hydrophobic organic compounds to organic material in the soil system." Licentiate thesis, Umeå universitet, Kemiska institutionen, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-68378.

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Contaminated soils and sediments have been identified as significant secondary sources of organic contaminants.  Leaching tests may be useful tools to estimate the mobility of contaminants via the water phase and thereby the risk for groundwater and surface water contamination. The influence of soil composition (peat and clay content) on the leachability was investigated in batch leaching experiments for chemically diverse hydrophobic organic compounds (HOCs: PCP, PAHs, HCB, HCHs, PCBs, and TCDD/Fs). The above mentioned compounds were analyzed by both GC-LRMS (gas chromatography coupled with low resolution mass spectrometry (GC-HRMS) and GC-HRMS (gas chromatography coupled with high resolution mass spectrometry). Also the the leachability of eleven selected PCBs from naturally aged soil (Västervik, Sweden) was investigated in relation to the composition and concentration of dissolved organic matter at different pH (2 to 9), using a pH static test with initial acid/base addition. The the composition and of dissolved organic matter (DOM) at different pH values was explored by FTIR spectroscopy. The results were evaluated by orthogonal projections to latent structures (OPLS). Generally, for all model compounds studies, the Kd-values showed a variability of 2-3 orders of magnitude depending on the matrix composition. The Kd-values of moderately hydrophobic compounds, (e.g. HCHs, PCP and Phe), were correlated mainly with the organic matter content of soil. For more hydrophobic compounds (e.g.BaA, HCB and PCB 47), the leachability decreased as the proportions of  OM and clay contents increased. The Kd-values of 1,3,6,8-TCDD and 1,3,6,8-TCDF were  positively correlated with peat content but negatively correlated with clay content, while for PCB 153 and PCB 155 the correlations were reversed. The log Kd-values of all target PCBs decreased with increased pH values and the log Kd-values were highly correlated with the concentration of total organic carbon (TOC) in the leachates. The FTIR analysis of DOM showed that the least chlorinated and hydrophobic PCB congeners (i.e. PCB 28) might be associated with the hydrophilic fraction (i.e. carboxylic groups) of DOM. Our study demonstrated how complex interaction between the organic matter, clay components, pH and DOC influences the leachability of HOCs in a compound-specific manner.
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Wee, Hun Young. "Remedial extraction and catalytic hydrodehalogenation for treatment of soils contaminated by halogenated hydrophobic organic compounds." [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-1280.

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Zehraoui, Abderrahman. "ENHANCED BIOLOGICAL OXIDATION OF HYDROPHOBIC COMPOUNDS UNDER DYNAMIC LOAD IN A TRICKLE BED AIR BIOFILTER." University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384849490.

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Pan, Wubin. "Regulation of the susceptibility of Neisseria gonorrhoeae to antibiotics and hydrophobic compounds by the mtr system." Thesis, University of Sussex, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238975.

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Jakubowska, Joanna. "Effect of irrigation water type on soil organic matter (SOM) fractions and their interactions with hydrophobic compounds /." Leipzig : UFZ, 2007. http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=015692639&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA.

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Books on the topic "Hydrophobic compounds"

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Filho, Murillo Villela. Enantioselective reduction of hydrophobic keto compounds in multiphase bioreactor. Jülich: Forschungszentrum, Zentralbibliothek, 2007.

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Laak, Thomas ter. Sorption to soil of hydrophobic and ionic organic compounds: Measurement and modeling = Sorptie van hydrofobe en ionogene organische stoffen aan bodem. [Utrecht]: Universiteit Utrecht, 2005.

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Pontolillo, James. The search for reliable aqueous solubility (Sw) and octanol-water partition coefficient (Kow) data for hydrophobic organic compounds: DDT and DDE as a case study. Reston, Va: U.S. Dept. of the Interior, U.S. Geological Survey, 2001.

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Westall, John C. The use of cationic surfactants to modify aquifer materials to reduce the mobility of hydrophobic organic compounds / John C. Westall ... [et al.]. Ada, OK: U.S. Environmental Protection Agency, Robert S. Kerr Environmental Research Laboratory, 1994.

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Westall, John C. The use of cationic surfactants to modify aquifer materials to reduce the mobility of hydrophobic organic compounds / John C. Westall ... [et al.]. Ada, OK: U.S. Environmental Protection Agency, Robert S. Kerr Environmental Research Laboratory, 1994.

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Barnat-Hunek, Danuta. Hydrofobizacja opoki wapnistej w obiektach zabytkowych Kazimierza Dolnego: Hydrophobisation of siliceous limestone in historic buildings of Kazimierz Dolny. Lublin: Wydawnictwo Politechniki Lubelskiej, 2010.

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Ochs, Michael. Association of hydrophobic organic compounds with dissolved soil organic carbon. 1988.

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Wu, Shian-chee. Transport of hydrophobic organic compounds between water and natural sediments. 1986.

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Tonekaboni, Madjid Mohseni. Biofiltration of hydrophilic and hydrophobic volatile organic compounds using wood-based media. 1998.

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Cork, Tracy D. The fate of hydrophobic organic compounds in soil systems: A kinetic model and sensitivity analysis. 1988.

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Book chapters on the topic "Hydrophobic compounds"

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Endo, Yasuyuki. "Carboranes as Hydrophobic Pharmacophores." In Boron-Based Compounds, 1–19. Chichester, UK: John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119275602.ch1.1.

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Farrington, John W. "Bioaccumulation of Hydrophobic Organic Pollutant Compounds." In Ecotoxicology: Problems and Approaches, 279–313. New York, NY: Springer New York, 1989. http://dx.doi.org/10.1007/978-1-4612-3520-0_11.

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Webster, G. R. Barrie, Mark R. Servos, G. Ghaus Choudhry, Leonard P. Sarna, and Derek C. G. Muir. "Methods for Dissolving Hydrophobic Compounds in Water." In Advances in Chemistry, 251–62. Washington, DC: American Chemical Society, 1988. http://dx.doi.org/10.1021/ba-1988-0219.ch017.

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Curtis, Gary P., Martin Reinhard, and Paul V. Roberts. "Sorption of Hydrophobic Organic Compounds by Sediments." In ACS Symposium Series, 191–216. Washington D.C.: American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0323.ch010.

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Valsaraj, K. T., X. Y. Lu, and L. J. Thibodeaux. "Removal of Hydrophobic Organic Compounds from the Aqueous Phase." In ACS Symposium Series, 116–28. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0509.ch009.

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Schwarzenbach, R. P. "Sorption Behavior of Neutral and Ionizable Hydrophobic Organic Compounds." In Organic Micropollutants in the Aquatic Environment, 168–77. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4660-6_20.

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Hayat, Tahir, Wen Xia, Yan He, Haizhen Wang, Jianjun Wu, and Jianming Xu. "Humic Substances as a Reductant for Hydrophobic Organic Compounds." In Functions of Natural Organic Matter in Changing Environment, 641–45. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-5634-2_116.

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Elzerman, Alan W., and John T. Coates. "Hydrophobic Organic Compounds on Sediments: Equilibria and Kinetics of Sorption." In Sources and Fates of Aquatic Pollutants, 263–317. Washington, DC: American Chemical Society, 1987. http://dx.doi.org/10.1021/ba-1987-0216.ch010.

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Grimaud, R. "Biofilm Development at Interfaces Between Hydrophobic Organic Compounds and Water." In Cellular Ecophysiology of Microbe, 1–10. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-20796-4_41-1.

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Grimaud, R. "Biofilm Development at Interfaces between Hydrophobic Organic Compounds and Water." In Handbook of Hydrocarbon and Lipid Microbiology, 1491–99. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-77587-4_102.

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Conference papers on the topic "Hydrophobic compounds"

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Xia, Xinghui, Haotian Wang, and Derek C. g. Muir. "Dietary Uptake Pattern Affects Bioaccumulation and Biomagnification of Hydrophobic Organic Compounds in Fish." In Goldschmidt2020. Geochemical Society, 2020. http://dx.doi.org/10.46427/gold2020.2919.

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Mahotkina, L. YU, and A. A. Halilova. "Development of hydrophobic textile materials for the production of working clothes using organosilicon compounds." In SCIENCE OF RUSSIA: GOALS AND OBJECTIVES. L-Journal, 2020. http://dx.doi.org/10.18411/sr-10-08-2020-18.

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Baruwa, Akinsanya Damilare, Esther Titilayo Akinlabi, O. P. Oladijo, and Frederick Mwema. "Structural and Mechanical Analysis of Silane Compounds Coatings on AISI 304." In ASME 2019 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/imece2019-10721.

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Abstract The structures and mechanical strength existing in three different hydrophobic silane compounds, Henicosyl-1,1,2,2-tetrahydrododecyltrichlorosilane (FDDTS), Tridecafloro-1,1,2,2-tetrahydrooctyltrichlorosilane (FOTS) and [Tris(trimethylsiloxy)silyethyl]dimethylchlorosilane (Alkyl) under same deposition conditions were studied and presented in this paper. The effect of the chemical composition on the mechanical strength and the structural evolutions as related to chlorosilane was inquired. The structures were investigated by using field emission scanning electron microscope (FESEM), atomic force microscope (AFM) and surface profiler while the nature of the mechanical strength was determined from nanoindentation and nano scratch. From the data obtained, the FDDTS showed to be denser in structures than both Alkyl and FOTS. The root-mean-square (RMS) roughness exhibited by FDDTS was larger when compared to the other two silanes. The mechanical ability shows that the FDDTS has the largest maximum penetration load as well as highest scratch resistance. Overall, the FDDTS would perform excellently in the applications where combine hard and wear resistance organic coating is required.
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Abe, Ryogo, Keita Takeuchi, Asuka Suzuki, Kosuke Watanabe, and Akihiko Kikuchi. "Fabrication of CH3NH3PbBr3 Based Perovskite Single Crystal Arrays by Spin-coating Method Using Hydrophobic Patterned Substrate." In 2019 Compound Semiconductor Week (CSW). IEEE, 2019. http://dx.doi.org/10.1109/iciprm.2019.8819242.

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Baruwa, Akinsanya Damilare, Oluseyi Philip Oladijo, Nthabiseng Maledi, and Esther Titilayo Akinlabi. "Influence of Surface Pretreatment on the Hydrophobic Silane Coating on AISI 304 Steel." In ASME 2018 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/imece2018-86256.

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The influence of surface pretreatment on the integrity of Tridecafloro-1,1,2,2-tetrahydrooctyltrichlorosilane (FOTS) coating on the substrate is presented. FOTS is a hydrophobic organic compound deposited on the SS 304 surface to enhance the corrosion protection of the metal. The surface was pretreated with silicon oxide, plasma oxide and both served as adhesions before the coating was deposited on the substrate by atomic layer deposition technique. The coatings were characterized by scanning electron microscope (morphology), atomic force microscope (surface roughness). The chemical composition and bonding structure were obtained by X-ray diffraction (XRD) and Attenuated-Fourier transform infrared (ATR-FTIR). The durability of the coating in corrosive media was investigated through electrochemical polarization and electrochemical impedance spectroscopy (EIS). The results obtained showed that silicon oxide pre-treated steel gave a better stability and improved properties to the coating than the plasma oxide pre-treated surface, and was distinctly discussed.
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Reports on the topic "Hydrophobic compounds"

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Lin, Xiao-Min, and Subramanian Sankaranarayanan. Ultrathin Nanoparticle Membranes to Remove Emerging Hydrophobic Trace Organic Compounds in Water with Low Applied Pressure and Energy Consumption. Office of Scientific and Technical Information (OSTI), February 2019. http://dx.doi.org/10.2172/1502835.

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The search for reliable aqueous solubility (Sw) and octanol-water partition coefficient (Kow) data for hydrophobic organic compounds; DDT and DDE as a case study. US Geological Survey, 2001. http://dx.doi.org/10.3133/wri014201.

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