• 제목/요약/키워드: Water chemistry

검색결과 4,424건 처리시간 0.03초

Determination of Polonium Nuclides in a Water Sample with Solvent Extraction Method

  • Lee, M.H.;Lee, C.H.;Song, K.;Kim, C.K.;Martin, P.
    • Bulletin of the Korean Chemical Society
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    • 제31권9호
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    • pp.2488-2492
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    • 2010
  • A method is described for the determination of the Po nuclides in a water sample. After the Po nuclides were purified from interfering elements in a water sample using a manganese dioxide precipitation followed by a solvent extraction method, the Po nuclides were deposited onto the silver plate. A large volume of the water sample was effectively pretreated with manganese dioxide precipitation method. To determine the optimum conditions for plating Po, the effects of the pH, volume, temperature and time on the Po deposition were investigated in hydrochloric acid solution. The investigated determination method of Po nuclides with solvent extraction was applied to a tap water sample.

Determination of Normal Saturated- and Polycyclic Aromatic Hydrocarbons in the River Water of Bangladesh by Liquid-Liquid Extraction and Gas Chromatography

  • Mottaleb, M.A.;Sarma, D.K.;Sultana, S.;Husain, M.M.;Alam, S.M.M.;Salehuddin, S.M.
    • Bulletin of the Korean Chemical Society
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    • 제24권1호
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    • pp.99-105
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    • 2003
  • A liquid-liquid extraction followed by evaporative concentration method was used to determine the concentration of normal, or straight chain, saturated hydrocarbons (NSH) $(C_{10}\;to\;C_{24})$ and polycyclic aromatic hydrocarbons (PAH) here defined as: fluorene, anthracene, pyrene, chrysene and perylene, in the Buriganga River water of Bangladesh. Samples were collected from 5 and 25 cm depth of water at the southern, middle and northern parts of the river at Postogolla, Sadarghat and Sowarighat stations. Hydrocarbons were extracted from 450 mL of water into 75 mL n-hexane and then concentrated into 1 or 2 mL solution by evaporation. These solutions were analyzed by gas chromatography. The highest and lowest concentrations were determined as $257\;{\mu}gL^{-1}\;for\;C_{13}\;and \;0.24\;{\mu}g\;L^{-1}\;for\;C_{22}$ at 5 ㎝ depth of water, at the northern part of the Sowarighat and southern part of the Postogolla, respectively. This method could allow the analysis of water for $C_{22}$ as low as $0.24\;{\mu}g\;L^{-1}$.

Trihalomethane formation potential of drinking water sources in a rural location

  • Rajamohan, R.;Ebenezer, Vinitha;Rajesh, Puspalata;Venugopalan, V.P.;Natesan, Usha;Murugesan, V.;Narasimhan, S.V.
    • Advances in environmental research
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    • 제1권3호
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    • pp.181-189
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    • 2012
  • Trihalomethanes, produced as a result of chlorination of drinking water, are considered a potential health hazard. The trihalomethane formation potential (THMFP) of a raw water source may indicate the maximum trihalomethanes (THMs) that are likely to be produced when chlorine reacts with natural organic matter (NOM) present in the water. A study was conducted to evaluate the THMFP in seven different drinking water sources in the vicinity of Kalpakkam, a rural township, on the east coast of India. Water from seven stations were analysed for THMFP. THMFP was compared with surrogate parameters such as dissolved organic carbon (DOC), ultraviolet absorbance ($UV_{254}$) and bromide. The data showed that THMFP was high in water from open wells as compared to closed bore wells, possibly due to more photosynthetic activity. Proximity to sea, and consequently the levels of bromide, was an important factor that influenced THM formation. THM surrogate parameters showed good correlation with THMFP.

Zundel- and Eigen-like Surface Hydrated Protons on Pt(111)

  • Kim, Youngsoon;Park, Youngwook;Shin, Sunghwan;Kang, Heon
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2016년도 제50회 동계 정기학술대회 초록집
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    • pp.167.1-167.1
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    • 2016
  • The interaction between adsorbed water and hydrogen on metallic surfaces is important for fundamental understanding of heterogeneous catalysis and electrode surface reactions in acidic environment. Here, we explore a long-standing question of whether hydronium ion can exist or not on a Pt surface coadsorbed with atomic hydrogen and water. Studies based on mass spectrometry and infrared spectroscopy show clear evidence that hydrogen atoms are converted into hydrated protons on a Pt(111) surface. The preferential structures of hydrated protons are identified as multiply hydrated $H_5O_2{^+}$ and $H_7O_3{^+}$ species rather than as hydronium ions. The multiply hydrated protons may be regarded as two dimensional zundel ($H_5O_2{^+}$) and Eigen cation ($H_7O_3{^+}$) in water-metal interface. These surface-bound hydrated protons may be key surface intermediates of the electrochemical interconversion between adsorbed hydrogen atoms and solvated protons.

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Change in Water Contact Angle of Carbon Contaminated TiO2 Surfaces by High-energy Electron Beam

  • Kim, Kwang-Dae;Tai, Wei Sheng;Kim, Young-Dok;Cho, Sang-Jin;Bae, In-Seob;Boo, Jin-Hyo;Lee, Byung-Cheol;Yang, Ki-Ho;Pack, Ok-Kyung
    • Bulletin of the Korean Chemical Society
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    • 제30권5호
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    • pp.1067-1070
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    • 2009
  • We studied change in water contact angle on $TiO_2$ surfaces upon high-energy electron-beam treatment. Depending on conditions of e-beam exposures, surface OH-content could be increased or decreased. In contrast, water contact angle continuously decreased with increasing e-beam exposure and energy, i.e. change in the water contact angle cannot be rationalized in terms of the overall change in the surfacestructure of carbon-contaminated $TiO_2$. In the C 1s spectra, we found that the C-O and C=O contents gradually increased with increasing e-beam energy, suggesting that the change in the surface structure of carbon layers can be important for understanding of the wettability change. Our results imply that the degree of oxidation of carbon impurity layers on oxide surfaces should be considered, in order to fully understand the change in the oxide surface wettability.

Advancement of Clay and Clay-based Materials in the Remediation of Aquatic Environments Contaminated with Heavy Metal Toxic Ions and Micro-pollutants

  • Lalhmunsiama, Lalhmunsiama;Malsawmdawngzela, Ralte;Vanlalhmingmawia, Chhakchhuak;Tiwari, Diwakar;Yoon, Yiyong
    • 공업화학
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    • 제33권5호
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    • pp.502-522
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    • 2022
  • Clay minerals are natural materials that show widespread applications in various branches of science, including environmental sciences, in particular the remediation of water contaminated with various water pollutants. Modified clays and minerals have attracted the attention of researchers in the recent past since the modified materials are seemingly more useful and efficient for removing emerging water contaminants. Therefore, modified engineered materials having multi-functionalities have received greater interest from researchers. The advanced clay-based materials are highly effective in the remediation of water contaminated with organic and inorganic contaminants, and these materials show enhanced selectivity towards the specific pollutants. The review inherently discusses various methods employed in the modification of clays and addresses the challenges in synthesizing the advanced engineered materials precursor to natural clay minerals. The changes in physical and chemical properties, as investigated by various characterization techniques before and after the modifications, are broadly explained. Further, the implications of these materials for the decontamination of waterbodies as contaminated with potential water pollutants are extensively discussed. Additionally, the insights involved in the removal of organic and inorganic pollutants are discussed in the review. Furthermore, the future perspectives and specific challenges in the scaling up of the treatment methods in technology development are included in this communication.