Готові списки джерел за темами / Chemical removal

Добірка наукової літератури з теми "Chemical removal"

Автор: Grafiati
Опубліковано: 15 червня 2024

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Зміст

  1. Статті в журналах
  2. Дисертації
  3. Книги
  4. Частини книг
  5. Тези доповідей конференцій
  6. Звіти організацій

Статті в журналах з теми "Chemical removal":

1

Fan, Jie, Han Hu, Ying Zhang, and Lei Zhu. "Biological Phosphorus Removal Combined with Ferrous Chemical Phosphorus Removal." Advanced Materials Research 955-959 (June 2014): 3339–42. http://dx.doi.org/10.4028/www.scientific.net/amr.955-959.3339.

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Chemical phosphorus removal is widely applied to enhance the biological phosphorus removal in order to meet the discharge requirement. Performance change caused by ferrous sulfate was investigated in this study. Compared to the control system which was not chemically dosed, pH and SVI slightly decreased while conductivity increased. The correlation between phosphorus and conductivity was weakened. The release and uptake of potassium declined, illustrating a negative impact of chemical precipitant on phosphorus accumulating organisms (PAO). The phosphorus uptake decreased while phosphorus release fluctuated. The phosphorus was not suitable for revealing the metabolic activity of PAO due to formation of ferric phosphate and ferric hydroxide.
2

Watanabe, Yoshimasa. "Phosphorous removal by chemical coagulation." Japan journal of water pollution research 11, no. 10 (1988): 611–16. http://dx.doi.org/10.2965/jswe1978.11.611.

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3

Zollitsch, Carsten. "Chemical Removal of Powder Coatings." JOT-International Surface Technology 4, no. 1 (January 2011): 36–37. http://dx.doi.org/10.1365/s35724-011-0015-5.

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4

Thistleton, J., T. Clark, P. Pearce, and S. A. Parsons. "Mechanisms of Chemical Phosphorus Removal." Process Safety and Environmental Protection 79, no. 6 (November 2001): 339–44. http://dx.doi.org/10.1205/095758201753373104.

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5

Taherabdollah, Ali, and Mustafa Abdullah. "Comparison of Removal of Chromium by using Natural and Chemical Adsorbents." International Journal of Science and Research (IJSR) 12, no. 9 (September 5, 2023): 642–45. http://dx.doi.org/10.21275/sr23903165126.

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6

Sharon, Vinitha. "Effect of Greywater Characteristics on its Chemical Coagulation." International Journal of Engineering Technology and Management Sciences 4, no. 2 (March 28, 2020): 1–6. http://dx.doi.org/10.46647/ijetms.2020.v04i02.001.

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The effect of physico-chemical characteristics of greywater on its chemical coagulation was assessed employing real greywater with varying characteristics using both alum and polyaluminium chloride (PACl) as coagulants. Optimum PACl dosages required were significantly less compared to alum for similar initial turbidity levels. Also, PACl produced less turbid treated greywater. As the initial pH increased, the optimum coagulant dose also increased for both alum and PACl. At similar optimum dosages, PACl gave higher COD removal compared to alum. Total coliform removal showed no significant difference with removals of 98.3% and 98.9%, respectively for alum and PACl.
7

Kono, Akihiko, Kenji Yada, Hideo Horibe, Hiromitsu Ota, and Motonori Yanagi. "Removal of Negative-tone Novolak Chemical Amplification Resist by Chemicals." KAGAKU KOGAKU RONBUNSHU 36, no. 6 (2010): 589–93. http://dx.doi.org/10.1252/kakoronbunshu.36.589.

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8

Altinbaş, M., C. Yangin, and I. Ozturk. "Struvite precipitation from anaerobically treated municipal and landfill wastewaters." Water Science and Technology 46, no. 9 (November 1, 2002): 271–78. http://dx.doi.org/10.2166/wst.2002.0257.

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A two-stage treatment system including upflow anaerobic sludge blanket reactor pre-treatment combined with a chemical post treatment system such as magnesium ammonium phosphate (MAP) precipitation was proposed as a comparable alternative to conventional biological treatment. In this study, anaerobically pre-treated domestic wastewater, domestic wastewater mixed with 2% and 3% of leachate by volume and raw leachate were further treated chemically with MAP precipitation. MAP precipitation was both applied at the stoichiometric ratio (Mg:NH4 = PO4; 1:1:1) and above the stoichiometric ratio (1.1:1:1 and 1.1:1:1.1) on domestic wastewater +3% leachate mixture. Maximum NH4-N removal of 68% was achieved at the pH of 9.2 at the stoichiometric ratio, whereas at the same pH value 70 to 72% NH4-N removal was obtained above the stoichiometric ratio. Additional ammonia recovery studies were conducted on Fenton's oxidation applied effluents before MAP precipitation and no significant additional ammonium removal was achieved. However, by the application of Fenton's oxidation high additional COD removals were obtained. Consequently, chemical treatment by MAP precipitation and/or Fenton's oxidation after anaerobic treatment yielded very effective removals for COD and NH4-N in domestic wastewaters + leachate mixtures.
9

Nedjah, Nawel, Oualid Hamdaoui, and Nabila Laskri. "Phosphorus Removal of Urban Wastewater by Physico- Chemical Treatment: Waterways Euthrophication Prevention." International Journal of Environmental Science and Development 6, no. 6 (2015): 435–38. http://dx.doi.org/10.7763/ijesd.2015.v6.632.

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10

Onawole, Abdulmujeeb T., Ibnelwaleed A. Hussein, Hassan I. Nimir, Musa E. M. Ahmed, and Mohammed A. Saad. "Molecular Design of Novel Chemicals for Iron Sulfide Scale Removal." Journal of Chemistry 2021 (February 5, 2021): 1–11. http://dx.doi.org/10.1155/2021/7698762.

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Scale deposition is a pertinent challenge in the oil and gas industry. Scales formed from iron sulfide are one of the troublous scales, particularly pyrite. Moreover, the use of biodegradable environmentally friendly chemicals reduces the cost compared to the conventional removal process. In this work, the chelating abilities of four novel chemicals, designed using the in silico technique of density functional theory (DFT), are studied as potential iron sulfide scale removers. Only one of the chemicals containing a hydroxamate functional group had a good chelating ability with Fe2+. The chelating strength and ecotoxicological properties of this chemical were compared to diethylenetriaminepentaacetic acid (DTPA), an already established iron sulfide scale remover. The new promising chemical surpassed DTPA in being a safer chemical and having a greater binding affinity to Fe2+ upon optimization, hence, a better choice. The presence of oxime (-NHOH) and carbonyl (C=O) moieties in the new chemical showed that the bidentate form of chelation is favored. Moreover, the presence of an intramolecular hydrogen bond enhanced its chelating ability.
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Статті в журналах Дисертації Книги

Дисертації з теми "Chemical removal":

1

Bernstein, Howard. "A system for heparin removal." Thesis, Massachusetts Institute of Technology, 1985. http://hdl.handle.net/1721.1/15291.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 1985.
MICROFICHE COPY AVAILABLE IN ARCHIVES AND SCIENCE.
Bibliography: leaves 255-264.
by Howard Bernstein.
Ph.D.
2

Gaulin, Jean-Philippe. "Selective caffeine removal by microbial consortia." Thesis, McGill University, 2003. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=80272.

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Coffee processing presents a considerable waste disposal problem, mainly because of the large volumes generated and the chemical composition of the by-products, particularly the caffeine levels. The use of Pseudomonas putida IF-3, a caffeine-degrading microorganism, in a microbial consortium for bioremediation of caffeine found in coffee wastes was investigated. Caffeine degradation was observed in fed-batch reactor experiments with caffeine as sole source of carbon and nitrogen. Metabolic regulation and caffeine removal potential by Pseudomonas putida IF-3 were investigated by supplementing with other nutrient sources. Diauxic growth was not observed. Nitrogen release from caffeine breakdown was found to be rate-limiting.
Effects of caffeine on microbial consortia were studied using denaturing gradient gel electrophoresis (DGGE), providing a community-scale view of changes in microbial consortia upon caffeine addition. Surprisingly, caffeine removal was achieved indigenously by the microbial consortium. Principal component analysis was used to analyze differences in DGGE banding patterns between control and caffeine-exposed mixed cultures.
3

Roostaei, Nadia. "Removal of phenol from water by adsorption." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0001/MQ46605.pdf.

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4

Abdulrahman, Aymn. "Removal of mixed acids from aqueous solution." Thesis, The University of Maine, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3662514.

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Carboxylic acids are commonly generated in biorefinery operations such as fermentation or aqueous extraction of hemicellulose feedstocks. In most cases, organic acids are generated as dilute components in aqueous streams. If they can be recovered from solution inexpensively they may find value as pure chemical products or as starting materials for a wide variety of organic products, including biofuels.

Liquid-liquid extraction is a separation method applied to recover mixed carboxylic acids from a fermented wood extract. These acids included: acetic, propionic, butyric, valeric, caproic and heptanoic acids. An organic solution, such as trialkylphosphine oxide (CYANEX 923, a mixture of four trialkylphosphine oxides), was mixed with fermented wood extract to extract these acids. Although the extraction was highly effective, however it was shown that distillation was not able to recover these acids from the extraction solvent.

In this study, after liquid-liquid extraction of the acids from the aqueous phase, the mixed acids are recovered from the organic phase by a back extraction with sodium hydroxide. The mixture is agitated and centrifuged to separate the organic and aqueous phases. Results present the extraction and recovery efficiencies of this method of recovery organic acids.

5

Ng, Dedy. "Nanoparticles removal in post-CMP (Chemical-Mechanical Polishing) cleaning." Thesis, Texas A&M University, 2005. http://hdl.handle.net/1969.1/4159.

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Research was performed to study the particle adhesion on the wafer surface after the chemical-mechanical polishing (CMP) process. The embedded particles can be abrasive particles from the slurry, debris from pad material, and particles of film being polished. Different methods of particle removal mechanism were investigated in order to find out the most effective technique. In post-CMP cleaning, surfactant was added in the solution. Results were compared with cleaning without surfactant and showed that cleaning was more effective with the combined interaction of the mechanical effort from the brush sweeping and the chemistry of the surfactant in the solution (i.e., tribochemical interaction). Numerical analysis was also performed to predict the particle removal rate with the addition of surfactants. The van der Waals forces present in the wafer-particle interface were calculated in order to find the energy required to remove the particle. Finally, the adhesion process was studied by modeling the van der Waals force as a function of separation distance between the particle and the surface. The successful adaptation of elasticity theory to nanoparticle-surface interaction brought insight into CMP cleaning mechanisms. The model tells us that it is not always the case that as the separation distance is decreased, the attraction force will be increased. The force value estimated can be used for slurry design and CMP process estimation.
6

Mahmud, Hassan. "Development of pervaporation membrane for volatile organic chemical removal." Thesis, University of Ottawa (Canada), 1996. http://hdl.handle.net/10393/9896.

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Pervaporation is a membrane based process which overcomes many of the deficiencies of current technologies for the removal/recovery of volatile organic chemicals (VOCs) from aqueous streams. In this process, VOCs from a liquid stream are driven across a permselective membrane and exit as a vapor due to the vacuum maintained in the downstream side of the membrane. Proven hydrophobic membranes used for pervaporation today suffer from limitations of mechanical stability, while membranes with superior mechanical characteristics do not possess sufficient selectivity to be useful for these applications. To overcome these limitations surface modifying macromolecules (SMMs) have been used as additives in the preparation of polyethersulfone (PES) membranes, which inherently have good mechanical characteristics but are intrinsically hydrophilic. This approach produced membranes with high hydrophobicity (based on contact angles), which were expected to be permselective to VOCs, like chloroform. This thesis investigates the impact of PES/SMM membrane preparation parameters on the reported separation of chloroform from aqueous solutions via pervaporation. These parameters include polyvinylpyrrolidone (PVP) addition levels, solution mixing period, solution age and membrane age. A chemical analysis of the permeate revealed that the permeate contained ethanol but virtually no chloroform. Permeate ethanol concentrations were higher with fresh membranes and decreased both with membrane age and period of use. This indicates that ethanol which was used during the solvent exchange drying step of membrane preparation, was being leached from the membrane. It was concluded that there was in fact no enrichment of chloroform in the permeate as reported earlier and that the surface hydrophobicity introduced was insufficient to dominate over the intrinsic bulk hydrophilic characteristics of the PES membranes. These findings indicate a need to reevaluate the levels of SMM addition and the process parameters to develop a sufficiently dominant hydrophobic surface layer.
7

Omoregie, Henryson Osawaru 1953. "Removal of chemical species by electrically charged bicomponent fibers." Diss., The University of Arizona, 1996. http://hdl.handle.net/10150/282121.

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A new water deionization method was conceived and investigated. Bench scale reactors were designed and tested. Numerical analysis of ion movement in water in the presence of electrical, hydraulic, and chemical gradients was conducted. The new water treatment technology uses bicomponent fibers (BCF). Ions in water are concentrated near charged bicomponent fibers. Bicomponent fibers are composed of two materials. The outer annulus is made of nylon and has an inside diameter of 10 mum and outer diameter of 50 mum. The inner annulus is composed of carbon powder and has an outer diameter of 10 mum. For the bench scale reactors, approximately one kilometer length of fibers was wrapped around a series of plastic panels and placed in a plexiglass container containing sodium nitrate solution. The ends of the fibers were covered with electrically conductive epoxy and connected to a DC power supply. In experiments which lasted up to 96 h., the solution showed up to 50 percent decrease in nitrate concentration after the power supply was applied. Preliminary studies indicated that distance between panels, polarity of panels and voltage magnitude influenced observed concentration. Two one dimensional analytical solutions and finite element solutions for two dimensions were derived for no flow condition between parallel plates. For the first finite element model, the continuity, Navier-Stokes, and species equations were solved for solute concentration with rectangular coordinates. For the second model, Poisson-Boltzmann equations were included in a finite element scheme. The models were applied to irregular-shaped bodies and the finite element solutions were compared with analytical solutions. The solutions for Poisson-Boltzmann equations were obtained for both linearized and non-linear forms. Boundary conditions included no chemical reactions and no transport across boundaries. The formulations did not solve for concentration in bicomponent fiber reactors because insufficient data and knowledge of the bicomponent fiber process is available. However, future numerical models of the bicomponent fiber treatment process may be based on solutions derived in this research.
8

Sundaram, Hari Prashanth. "SO₂ removal with coal scrubbing." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2035.

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Thesis (M.S.)--West Virginia University, 2001.
Title from document title page. Document formatted into pages; contains vii, 42 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 33-34).
9

Shieh, Marvin Bryan. "Face-up chemical mechanical polishing : kinematics and material removal rate." Thesis, Massachusetts Institute of Technology, 2006. http://hdl.handle.net/1721.1/36701.

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Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2006.
Includes bibliographical references (leaf 27).
A working prototype face-up CMP tool has successfully been completed. Experiments conducted on the face-up CMP machine qualitatively correspond with the theoretical polishing model. Discrepancies in data from the theoretical model could potentially be caused by non-uniform loading of the polishing pad and uneven distribution of slurry over the pad due to the edge effects on fluid flow. Despite the discrepancies, experimental data suggest that the theoretical model used to describe blanket wafer polishing by the face-up CMP tool is at least partially valid.
by Marvin Bryan Shieh.
S.B.
10

Chua, Xiang Le. "Derivatisation of chemical warfare agent degradant without removal of water." Thesis, Chua, Xiang Le (2018) Derivatisation of chemical warfare agent degradant without removal of water. Masters by Coursework thesis, Murdoch University, 2018. https://researchrepository.murdoch.edu.au/id/eprint/42915/.

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Degradation products are distinct chemical signature for the detection of chemical warfare agents and forensic attribution in cases where the parent compound no longer exists. Being the common degradant to nerve agents, methylphosphonic acid serves as an explicit biomarker for the use of nerve agents. However, this non-volatile compound requires derivatisation prior to its detection, which incurs time-limiting factor and error. Therefore, development for a novel rapid and simple approach for identifying these degradants is of high importance to shed light on the use of chemical warfare agents and remediation of impacts. With the success of a recent pilot study for derivatisation of methylphosphonic acid without elimination of water, a subsequent quantitative study can be proceeded to assess on its practicality and efficiency.
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Книги з теми "Chemical removal":

1

Water Environment Federation. Task Force on Biological and Chemical Systems for Nutrient Removal. and Water Environment Federation. Municipal Subcommittee., eds. Biological and chemical systems for nutrient removal: A special publication. Alexandria, Va: Water Environment Federation, 1998.

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2

Wong, L. Biological removal and chemical recovery of metals from sludges. West Lafayette, IN: Purdue University Press, 1985.

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3

Randy, Merritt, Williamson Ashley D, and United States. Environmental Protection Agency. Control Technology Center, eds. Evaluation of a liquid chemical scrubber system for styrene removal. Research Triangle Park, NC: U.S. Environmental Protection Agency, Control Technology Center, 1994.

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4

Orzechowska, Grazyna E. Potential use of ultrasound in chemical monitoring. Las Vegas, Nev: Environmental Monitoring Systems Laboratory-Las Vegas, Office of Resarch and Development, U.S. Environmental Protection Agency, 1994.

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5

Batts, Robert Alan. Chemical phosphorus removal from wastewaters: A laboratory and pilot scale study. Birmingham: University of Birmingham, 1996.

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6

F, Hock V., US Army Center for Public Works., and Construction Engineering Research Laboratories (U.S.), eds. Demonstration of lead-based paint removal and chemical stabilization using Blastox®. Alexandria, VA: U.S. Army Center Public Works, 1996.

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7

Randy, Merritt, Williamson Ashley D, and Air and Energy Engineering Research Laboratory, eds. Evaluation of a liquid chemical scrubber system for styrene removal: Project summary. Research Triangle Park, NC: U.S. Environmental Protection Agency, Air and Energy Engineering Research Laboratory, 1995.

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8

Evanson, Ian Edward John. Removal of volatile organic compounds by absorption with catalytic enhanced chemical reaction. Birmingham: University of Birmingham, 1999.

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9

P, Huang C., and Water Environment Research Foundation, eds. Chemical characteristics and solids uptake of heavy metals in wastewater treatment: Project 93-CTS-1. Alexandria, VA: Water Environment Research Foundation, 2000.

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10

Lofrano, Giusy. Emerging compounds removal from wastewater: Natural and solar based treatments. Dordrecht: Springer, 2012.

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Частини книг з теми "Chemical removal":

1

Zhao, Wenyi. "Methods for Impurity Removal." In Handbook for Chemical Process Research and Development, Second Edition, 747–74. 2nd ed. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003288411-20.

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2

Henze, Mogens, and Poul Harremoës. "Chemical-Biological Nutrient Removal — The HYPRO Concept." In Chemical Water and Wastewater Treatment, 499–510. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-76093-8_33.

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3

Eikebrokk, Bjørnar. "Removal of Humic Substances by Coagulation." In Chemical Water and Wastewater Treatment IV, 173–87. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61196-4_15.

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4

Rott, Ulrich. "Magnetic Floc Separation in Chemical Phosphate Removal." In Chemical Water and Wastewater Treatment II, 497–505. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-77827-8_33.

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5

Kaviya, S. "Physical and Chemical Methods for Selenium Removal." In Selenium Contamination in Water, 181–205. Chichester, UK: John Wiley & Sons, Ltd, 2021. http://dx.doi.org/10.1002/9781119693567.ch10.

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6

Zhao, Wenyi. "Methods for Residual Metal Removal." In Handbook for Chemical Process Research and Development, Second Edition, 713–46. 2nd ed. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003288411-19.

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7

Tadini, Pietro, Urbano Tancredi, Michele Grassi, Carmen Pardini, Luciano Anselmo, Toru Shimada, and Luigi T. DeLuca. "Comparison of Chemical Propulsion Solutions for Large Space Debris Active Removal." In Chemical Rocket Propulsion, 985–1011. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-27748-6_41.

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8

Sidebottom, H. W., O. Rattigan, J. J. Treacy, and O. J. Nielsen. "Atmospheric Removal Processes for Chlorine-Containing Compounds." In Physico-Chemical Behaviour of Atmospheric Pollutants, 220–24. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0567-2_34.

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9

Storhaug, Ragnar, and Bjørn Rusten. "Upgrading a Primary Treatment Plant for Nutrient Removal." In Chemical Water and Wastewater Treatment, 461–70. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-76093-8_30.

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10

Scrano, Laura, Luca Foti, and F. Lelario. "Fluoroquinolones in Water: Removal Attemps by Innovative Aops." In Toxic Chemical and Biological Agents, 259–63. Dordrecht: Springer Netherlands, 2020. http://dx.doi.org/10.1007/978-94-024-2041-8_27.

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Тези доповідей конференцій з теми "Chemical removal":

1

Nieva, Aileen D., and Kathleen Mae A. Cedula. "Removal of Oxytetracycline in Simulated Wastewater by Coagulation." In Annual International Conference on Chemistry, Chemical Engineering and Chemical Process. Global Science & Technology Forum (GSTF), 2013. http://dx.doi.org/10.5176/2301-3761_ccecp.46.

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2

Petrus, Roman, Jolanta Warchoł, Waldemar Prokop, and Magdalena Warzybok. "Removal of Volatile Organic Compounds (VOCs) on synthesized zeolites." In Chemical technology and engineering. Lviv Polytechnic National University, 2019. http://dx.doi.org/10.23939/cte2019.01.332.

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3

Zhang, Yuhua, and Li Wei. "Physio-chemical treatment technologies for chromium removal." In 4th International Conference on Renewable Energy and Environmental Technology (ICREET 2016). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/icreet-16.2017.29.

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4

Yeo, Jin-Hee, Yun-Young Park, and Jae-Hwan Choi. "Enhancement of Selective Removal of Nitrate Using a Nitrate-Selective Composite Carbon Electrode." In Annual International Conference on Chemistry, Chemical Engineering and Chemical Process. Global Science & Technology Forum (GSTF), 2013. http://dx.doi.org/10.5176/2301-3761_ccecp.29.

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5

Shaw, J. C., R. Tsuen, and S. M. Leggitt. "Well Productivity Improvement by Chemical Removal of Pyrobitumen." In International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 1997. http://dx.doi.org/10.2118/37226-ms.

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6

Jo A DeBusk, Jactone Arogo Ogejo, Katharine F Knowlton, and Nancy G Love. "Chemical Phosphorus Removal for Separated Flushed Dairy Manure." In 2008 Providence, Rhode Island, June 29 - July 2, 2008. St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2008. http://dx.doi.org/10.13031/2013.32037.

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7

Busnaina, Ahmed A., and Naim Moumen. "Slurry Residue Removal in Post Chemical Mechanical Polishing." In ASME 1999 Design Engineering Technical Conferences. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/detc99/cie-9049.

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Анотація:
Abstract The megasonic cleaning process proved to be an essential process in cleaning silicon wafers after processes such as pre-oxidation, pre-CVD, pre-EPI, post-ASH and lately post-CMP. Current post-CMP cleans are contact cleaning techniques. These contact techniques have a low throughput and may cause wafer scratching. In addition, in contact cleaning, brush shedding which occurs under many operating conditions causes additional particulate contamination. There is a need for an effective post-CMP cleaning process. Megasonic cleaning provides the best alternative or compliment to brush clean.
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Xie, Lei, and Sai Wang. "Removal of uranium by cyclodextrin modified carbon nanoutubes." In 11TH ASIAN CONFERENCE ON CHEMICAL SENSORS: (ACCS2015). Author(s), 2017. http://dx.doi.org/10.1063/1.4977268.

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9

"Removal and Mineralization of Bisphenol A by Ozonation." In International Conference on Chemical, Agricultural and Medical Sciences. International Institute of Chemical, Biological & Environmental Engineering, 2014. http://dx.doi.org/10.15242/iicbe.c514017.

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Ammar, Reyhan, Julia Nieto-Sandoval, Santiago Esplugas, and Carme Sans. "On the nanoplastics removal by homogeneous catalytic ozonation." In 15th Mediterranean Congress of Chemical Engineering (MeCCE-15). Grupo Pacífico, 2023. http://dx.doi.org/10.48158/mecce-15.t3-o-15.

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Звіти організацій з теми "Chemical removal":

1

Martino, C., D. Herman, J. Pike, and T. Peters. ACTINIDE REMOVAL PROCESS SAMPLE ANALYSIS, CHEMICAL MODELING, AND FILTRATION EVALUATION. Office of Scientific and Technical Information (OSTI), June 2014. http://dx.doi.org/10.2172/1134065.

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2

Raphaelian, L. A. Combined chemical and microbiological removal of organic sulfur from coal. Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/6148180.

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3

Kaste, P. J., R. G. Daniel, R. A. Pesce-Rodriguez, M. A. Schroeder, and J. A. Escarsega. Hydrogen Plasma Removal of Military Paints: Chemical Characterization of Samples. Fort Belvoir, VA: Defense Technical Information Center, October 1998. http://dx.doi.org/10.21236/ada354821.

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4

Setser, D. W. Chemical Reactions of NCL(A Sup 1 Delta): Generation and Removal. Fort Belvoir, VA: Defense Technical Information Center, March 1999. http://dx.doi.org/10.21236/ada380849.

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5

Gray, D., and A. Sawy. Chemical and biodesulfurization systems for removal of organic sulfur from coal. Office of Scientific and Technical Information (OSTI), May 1990. http://dx.doi.org/10.2172/6895418.

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6

Gallagher, J., T. San, and G. Mayer. Removal of color and residual chemical oxygen demand from synfuel wastewater. Office of Scientific and Technical Information (OSTI), June 1988. http://dx.doi.org/10.2172/6893041.

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7

Gates, D. D., K. K. Chao, and P. A. Cameron. The removal of mercury from solid mixed waste using chemical leaching processes. Office of Scientific and Technical Information (OSTI), July 1995. http://dx.doi.org/10.2172/95487.

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8

Bauer, C. B., R. D. Rogers, L. Nunez, M. D. Ziemer, T. T. Pleune, and G. F. Vandegrift. Review and evaluation of extractants for strontium removal using magnetically assisted chemical separation. Office of Scientific and Technical Information (OSTI), November 1995. http://dx.doi.org/10.2172/219548.

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9

Cundiff, Charles H., Robert M. Leverette, and Jason R. Varner. Low Volatile Organic Compound (VOC) Chemical Agent Resistant Coating (CARC) Removal and Disposal. Fort Belvoir, VA: Defense Technical Information Center, February 2001. http://dx.doi.org/10.21236/ada388926.

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10

Dai, Y., and C. J. King. Modeling of fermentation with continuous lactic acid removal by extraction utilizing reversible chemical complexation. Office of Scientific and Technical Information (OSTI), July 1995. http://dx.doi.org/10.2172/90681.

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