Temat: cadmium (II) - Katalog OPAC zbiorów

Skocz do pozycji: 1.

Tytuł:: Water Purification from Ions of Cadmium (II) Using a Bio-Plateau
Autorzy:: Lapan, Oksana
Mikhyeyev, Oleksandr
Madzhd, Svitlana
Dmytrukha, Tetyana
Cherniak, Larysa
Petrusenko, Valentyna
Powiązania:: https://bibliotekanauki.pl/articles/123841.pdf
Data publikacji:: 2019
Wydawca:: Polskie Towarzystwo Inżynierii Ekologicznej
Tematy:: phytoremediation
bio-plateau
terrestrial plant
cadmium(II)
Opis:: The study was conducted with the purpose of experimentally developing the method of water purification from ions of cadmium (II) using a new design of a bio-plateau, which is based on the use of terrestrial plants. In order to construct the bio–plateau, the following chemically inert floating materials were used as the substrate: perlite, expanded clay, granular foam, vermiculite, cork, on top of which the seeds of higher terrestrial plants were placed. The experimental data showed that foam was the best of the tested substrates, and of plants – barley, oats, corn and rye. The constructed bio-plateau was placed into tanks with a solution of cadmium on the 9th day of incubation to study the cleaning efficiency of terrestrial plants on the aquatic environment. Determination of the residual concentration of cadmium was performed with the method of AAC at λ=228.8. As a result, it was found that rye showed the best sorption properties of the tested plants. The influence of additional aeration and pH of the medium on the degree of water purification was established. The highest treatment efficiency was observed in the variant of a bio-plateau with aeration and at a pH of 8-9. The study shows the possibility of using terrestrial plants for the phytoremediation of water bodies.
Źródło:: Journal of Ecological Engineering; 2019, 20, 11; 29-34
2299-8993
Pojawia się w:: Journal of Ecological Engineering
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 2.

Tytuł:: Lead(II) removal from aqueous solutions by solvent extraction with tetracarboxylresorcin[4]arene
Autorzy:: Konczyk, J.
Kozlowski, C.
Walkowiak, W.
Powiązania:: https://bibliotekanauki.pl/articles/110670.pdf
Data publikacji:: 2013
Wydawca:: Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:: solvent extraction
lead(II)
zinc(II)
cadmium(II)
resorcinarene
Opis:: A novel tetracarboxylresorcin[4]arene was synthesized and its selective complexing ability towards Pb(II) ions was examined. The influence of several parameters such as pH of aqueous phase, agitation time, extractant and modifier concentrations on solvent extraction of Pb(II) ions from the aque-ous nitrate phase into chloroform organic phase was studied. The stoichiometry of the formed metal-ligand complexes was established by slope analysis. Pb(II) ions were quantitatively extracted in the form of 2:1 Pb(II)-resorcin[4]arene complex from aqueous solutions of pH 5.5 to the solution of ligand in chloroform. Competitive solvent extraction experiments in the presence of Zn(II) and Cd(II) ions were also carried out and high selectivity of the extractant towards Pb(II) over Zn(II) and Cd(II) was found. The selectivity order was: Pb(II) >> Cd(II) > Zn(II).
Źródło:: Physicochemical Problems of Mineral Processing; 2013, 49, 1; 213-222
1643-1049
2084-4735
Pojawia się w:: Physicochemical Problems of Mineral Processing
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 3.

Tytuł:: N-(diethylthiophosphoryl)-aza[18]crown-6: synthesis and ability of solvent extraction toward lead(II), zinc(II) and cadmium(II) metal cations
Autorzy:: Kozlowska, J.
Miroshnichenko, S.
Powiązania:: https://bibliotekanauki.pl/articles/346955.pdf
Data publikacji:: 2013
Wydawca:: Politechnika Bydgoska im. Jana i Jędrzeja Śniadeckich. Wydział Technologii i Inżynierii Chemicznej
Tematy:: crown ethers
solvent extraction
lead(II)
zinc(II)
cadmium(II)
Opis:: This work presents the synthesis of a strongly hydrophobic, functionalized monaza crown ether, i.e., lariat ether, namely N-(diethylthiophosphoryl)-aza[18]crown-6 and its application as ion extractant in solvent extraction systems. The synthesis of thiophosphorylated aza[18]crown-6 was performed with good yield. Separation systems have been successfully developed to extract Pb(II), Cd(II) and Zn(II) into organic phase, i.e., chloroform with the crown ethers: aza[18]crown-6 and N-(diethylthiophosphoryl)-aza[18] crown-6 as extractants. The selectivity order in both crown ethers was Pb(II) >> Cd(II) > Zn(II). The obtained results suggest that N-(diethylthiophosphoryl)-aza[18]crown-6 can be used for the selective removal of Pb(II) at lower pH values than aza[18]crown-6.
Źródło:: Ars Separatoria Acta; 2012-2013, 9/10; 7-14
1731-6340
Pojawia się w:: Ars Separatoria Acta
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 4.

Tytuł:: Extraction properties of tetraheptylresorcin[4]arenes in relation to Cr(III) ions
Autorzy:: Konczyk, J.
Miroshnychenko, S.
Kozlowski, C.
Powiązania:: https://bibliotekanauki.pl/articles/109751.pdf
Data publikacji:: 2016
Wydawca:: Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:: solvent extraction
resorcin[4]arenes
chromium(III)
cadmium(II)
zinc ions
Opis:: Resorcin[4]arene-based ligand bearing four heptyl chains at the lower rim of the molecule was prepared and modified by four tetradietoxyphosphoryl groups in the upper rim. The compounds obtained were characterized by NMR spectroscopy and their extractability toward chromium(III) ions was studied. The influence of process parameters such as the pH of aqueous phase, agitation time and also extractant’s structure and concentration on efficiency of Cr(III) ions solvent extraction is presented. The highest yield of Cr(III) solvent extraction was obtained for two-hour agitation time of 5.010−4 M metal solution of pH 5.0 and 5.010−3 M chloroform solution of the tetradietoxyphosphorylated derivative of heptyl-resorcin[4]arene. Under optimal conditions, competitive solvent extraction of Cr(III), Zn(II), and Cd(II) ions was performed and separation factor values were established as 77.0 and 24.9 for Cr(III)/Cd(II) and Cr(III)/Zn(II) ions pairs, respectively. The stoichiometry of formed metal-ligand complexes 1:1 was found by classical slope analysis method.
Źródło:: Physicochemical Problems of Mineral Processing; 2016, 52, 2; 835-844
1643-1049
2084-4735
Pojawia się w:: Physicochemical Problems of Mineral Processing
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 5.

Tytuł:: Zinc(II) selective removal from other transition metal ions by solvent extraction and transport through polymer inclusion membranes with D2EHPA
Autorzy:: Ulewicz, M.
Walkowiak, W.
Pośpiech, B.
Powiązania:: https://bibliotekanauki.pl/articles/346997.pdf
Data publikacji:: 2003
Wydawca:: Politechnika Bydgoska im. Jana i Jędrzeja Śniadeckich. Wydział Technologii i Inżynierii Chemicznej
Tematy:: polymer inclusion membrane
solvent extraction
zinc(II)
cobalt(II)
nickel(II)
copper(II)
cadmium(II)
Opis:: An experimental investigation concerns zinc(II), cobalt(II), nickel(II), copper(II) and cadmium(II) ions separation from aqueous chloride solutions by solvent extraction and transport through polymer inclusion membrane (PIM) processes. The selective transport of metal ions from the aqueous chloride source phase through PIM containing cellulose triacetate (support), o-nitrophenyl pentyl ether (plasticizer) and di(2-ethylhexyl)phosphoric acid (ion carrier) is shown. Zn(II) can be effectively removed from dilute aqueous chloride solutions by its transport through PIMs with di(2-ethylhexyl)phosphoric acid as the ionic carriers into 1.0 M HCl as the receiving phase. The transport selectivity of Zn(II) over Co(II), Ni(II), Cu(II) and Cd(II) decreases while the pH of the solution increases in the source phase. Also, by solvent extraction, Zn(II) can be selectively removed from dilute aqueous chloride solutions.
Źródło:: Ars Separatoria Acta; 2003, 2; 47-55
1731-6340
Pojawia się w:: Ars Separatoria Acta
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 6.

Tytuł:: Transport of transition metal ions through polymer inclusion membranes with Cyanex 301
Autorzy:: Ulewicz, M.
Powiązania:: https://bibliotekanauki.pl/articles/347064.pdf
Data publikacji:: 2004
Wydawca:: Politechnika Bydgoska im. Jana i Jędrzeja Śniadeckich. Wydział Technologii i Inżynierii Chemicznej
Tematy:: polymer inclusion membrane
zinc(II)
cadmium(II)
copper(II)
cobalt(II)
nickel(II)
Cyanex 301
Opis:: The selective transport of zinc(II) and cadmium(II) ions from aqueous chloride or sulfate source phase through polymer inclusion membranes (PIM) containing cellulose triacetate (support), o-nitrophenyl pentyl ether (plasticizer) and di(2,4,4-trimethylpentyl)dithiophosphinic acid - Cyanex 301 (ion carrier) is shown. Zn(II) and Cd(II) ions can be effectively removed from dilute chloride and sulfate aqueous solutions into 1.0 M HCl or H2SO4 as the receiving phase. The separation coefficients were practically constant for acid concentrations in the receiving phase ranging from 0.01 to 1.0 M Copper(II), zinc(II), cadmium(II), cobalt(II), and nickel(II) ions removal from aqueous chloride solutions in transport through PIMs is also shown. These metal ions can be effectively removed from dilute aqueous chloride solutions in transport through PIMs with di(2,4,4-trimethylpentyl)dithiophosphinic acid as the ionic carriers into 1.0 M HCl. The selectivity coefficients of Cu(II) over Zn(II), Cd(II), Co(II) and Ni(II) were low and decreased with an increase in the pH of source aqueous phase.
Źródło:: Ars Separatoria Acta; 2004, 3; 81-88
1731-6340
Pojawia się w:: Ars Separatoria Acta
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 7.

Tytuł:: The use of the steric effect of the carrier molecule in the polymer inclusion membranes for the separation of cobalt(II), nickel(II), copper(II), and zinc(II) ions
Autorzy:: Radzyminska-Lenarcik, E.
Ulewicz, M.
Powiązania:: https://bibliotekanauki.pl/articles/778754.pdf
Data publikacji:: 2015
Wydawca:: Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:: polymer inclusion membrane
separation ions
steric effect
copper(II)
cobalt(II)
nickel(II)
cadmium(II)
zinc(II)
alkylimidazole
Opis:: In this study, palladium-modified nickel foam substrate was applied to examine ethanol oxidation reaction (EOR) in 0.1 The transport of cobalt(II), nickel(II), copper(II), and zinc(II) ions from chloride solutions across polymer inclusion membranes (PIMs), which 1-heptylimidazole (1̲) or 1-heptyl-2-methylimidazole (2̲) or 1-heptyl-4-methylimidazole (3̲) as the ion carrier was reported. The steric effect for carriers 2̲&enspand 3̲&enspdecreases the transport of all ions except Cu(II). The initial fluxes of metal ions transport across PIMs with the 1̲- 2̲&enspdecrease in the sequence: Cu(II) > Zn(II) > Co(II) > Ni(II), whereas for 3 they were Cu(II) > Zn(II) > Ni(II) > Co(II). The highest recovery values were obtained for Cu(II), this being 99 and 85% for carrier 1̲&enspand 2̲, respectively. In both membranes the degree of deposition of the Zn(II) ions was comparable. Zn(II), Co(II) and Cd(II) ions, which form complexes with coordination numbers 4 and 6, are more easily recovered with the use of carriers 2̲&enspand 3̲. Ni(II) ions, which form complexes with coordination number 6 only, practically remain in the feeding phase. PIMs with alkylimidazoles were characterized by non-contact atomic force microscopy.
Źródło:: Polish Journal of Chemical Technology; 2015, 17, 2; 51-56
1509-8117
1899-4741
Pojawia się w:: Polish Journal of Chemical Technology
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 8.

Tytuł:: Separation Of Cadmium(II), Cobalt(II) And Nickel(II) By Transport Through Polymer Inclusion Membranes With Phosphonium Ionic Liquid As Ion Carrier
Separacja jonów kadmu(II), kobaltu(II) i niklu(II) w procesie transportu przez polimerowe membrany inkluzyjne zawierające fosfoniową ciecz jonową w roli przenośnika
Autorzy:: Pospiech, B.
Powiązania:: https://bibliotekanauki.pl/articles/352721.pdf
Data publikacji:: 2015
Wydawca:: Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:: cadmium(II)
cobalt(II)
nickel(II)
Cyphos IL 101
polymer inclusion membrane
kadm(II)
nikiel(II)
kobalt(II)
polimerowe membrany inkluzyjne
Opis:: This paper presents study on the facilitated transport of cadmium(II), cobalt(II) and nickel(II) ions from aqueous chloride solutions through polymer inclusion membranes (PIMs) with phosphonium ionic liquid. Cyphos IL 101 (trihexyl(tetradecyl) phosphonium chloride) was used as a selective carrier for synthesis of cellulose triacetate membranes containing o-nitrophenyl pentyl ether (ONPPE) as a plasticizer. Effect of different parameters such as hydrochloric acid concentration in the source phase as well as ion carrier concentration in the polymer membrane on metal ions transport has been investigated. Cd(II) was transported preferably from hydrochloric acid solutions containing Co(II) and Ni(II) through PIM containing 18.8 wt.% CTA and 26.0 wt.% Cyphos 101 and 55.1 wt.% ONPPE into 0.5 M HNO3 as the receiving phase. The obtained results suggest that there is a possibility of application of this membrane with Cyphos IL 101 as ion carrier for separation of Cd(II) over Co(II) and Ni(II) from hydrochloric acid solutions.
Przeprowadzono badania transportu jonów Cd(II), Ni(II) i Co(II) z wodnych roztworów kwasu solnego przez polimerowe membrany inkluzyjne (PIMs) zawierające fosfoniową ciecz jonową – Cyphos IL 101 (chlorek triheksylo(tetradecylo) fosfoniowy) w roli selektywnego przenośnika jonowego. Rolę polimerowej matrycy w membranie pełnił trioctan celulozy (CTA). Jako plastyfikatora użyto eteru nitrofenylopentylowego (ONPPE). W wyniku badań określono wpływ różnych czynników, takich jak stężenie kwasu solnego w fazie zasilającej, jak również stężenie przenośnika w polimerowej membranie na selektywność i efektywność transportu badanych jonów metali. Jony kadmu(II) były selektywnie transportowane z roztworów kwasu solnego zawierającego jony niklu(II) i kobaltu(II) do 0,5 M roztworu kwasu azotowego(V). Uzyskane wyniki wskazują, że istnieje możliwość zastosowania procesów transportu przez polimerowe membrany inkluzyjne z cieczą jonową w roli selektywnego przenośnika do rozdzielania jonów Cd(II) od Ni(II) i Co(II) z roztworów kwasu solnego.
Źródło:: Archives of Metallurgy and Materials; 2015, 60, 4; 2933-2938
1733-3490
Pojawia się w:: Archives of Metallurgy and Materials
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 9.

Tytuł:: Modeling and analysis of batch extraction process for efficient removal of cadmium and pathogens from aqueous solution using modified plantain peel biochar
Autorzy:: Nworie, F. S.
Oti, W. O.
Nwali, U.
Powiązania:: https://bibliotekanauki.pl/articles/1193435.pdf
Data publikacji:: 2021
Wydawca:: Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:: Aspergillus
Biochar
Candida
Escherichia coli
Pseudomonas aeuroginosa
Staphylococcus aureus
cadmium (II)
equilibrium studies
mass transfer
pathogens
Opis:: Consumption of water contaminated with pathogens and heavy metals is responsible for the demise of millions of people around the globe. To find a low cost, facile and benign route for developing a biosorbent capable of handling the challenges associated with unsafe drinking water, the study report the preparation, activation, adsorption and removal of cadmium and pathogenic organisms from water samples. Modified plantain peel biochar (MPPB) was characterized using Braunauer-Emmett-Teller (BET) surface area and X-Ray diffraction (XRD). Surface area and pore size of the MPPB determined from BET surface area plot are 8.79 cc/g and 16.69 m2/g respectively with XRD crystallite size of 14.56 nm. The maximum adsorption capacity was observed to be 366.300 mmolkg-1. Equilibrium isotherm indicated the coefficient of determination to increase from Jovanovich →Elovic→Temkin→Freundlich→Langmuir model. Surface interaction and mass transfer kinetics shows a mixture of intra-particle diffusion and mass transfer process. The adsorption kinetics and surface interaction models coefficient of determination increased from Bangham pore diffusion →mass transfer model→Liquid film diffusion→pseudo first order→Dunwald-Wagner→Elovic→Pseudo-second order→Weber and Moris model. The adsorption indicated a chemisorption process with rate limitimg step likely to involve electron pair donor-acceptor interactions, hydrogen bonding and dipole dipole interactions. Antimicrobial evaluation of MPPB showed that it is a potential antimicrobial agent against common micro-organisms.
Źródło:: World Scientific News; 2021, 157; 1-24
2392-2192
Pojawia się w:: World Scientific News
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 10.

Tytuł:: Struktura i właściwości fizykochemiczne polimerów koordynacyjnych oraz materiałów typu MOF kadmu(II) i cynku(II)
Structure and physicochemical properties of coordination polymers and MOF materials based on cadmium(II) and zinc(II)
Autorzy:: Pobłocki, Kacper
Drzeżdżon, Joanna
Jacewicz, Dagmara
Powiązania:: https://bibliotekanauki.pl/articles/1413238.pdf
Data publikacji:: 2021
Wydawca:: Polskie Towarzystwo Chemiczne
Tematy:: polimery koordynacyjne
sieci metaliczno-organiczne
związki kadmu(II)
związki cynku(II)
MOF
coordination polymer
metal organic framework
cadmium(II)
compounds
zinc(II) compounds
Opis:: In 1964, J.C. Bailat Jr. was one of the first scientists who use coordination polymers in his research. He established the rules of structure and the composition of compounds containing metal ions and organic ligands connected by coordination bonds to form layered or chain structures. He compared inorganic compounds belonging to polymeric species with organic polymers. The term Metal Organic Frameworks (MOF) was first used in the publication by О. M. Yaghia. Crystalline, microporous structures contain rigid organic ligands (used interchangeably: organic building blocks) that bind metal ions. This is called reticular synthesis. MOF surface area values usually range from 1000 to 10000 m2/g-1, thus exceeding the area values of traditional porous materials such as zeolites and carbons. Metal Organic Frameworks create porous three-dimensional structures, unlike coordination polymers. Inorganic minerals from the aluminosilicate group are used in the widespread heterogeneous catalysis and processes such as: adsorption and ion exchange, while compared to Metal Organic Frameworks, shows a lower potential than zeolites, moreover, the design of structures is less precise and rational due to the lack of shape, size and control functionalization of pores. To date, MOF are the most diverse and most numerous class of porous materials. All aspects have made them ideal structures for storing fuels such as hydrogen and methane. They are perfect for catalytic reactions and are good materials for capturing pollutants, e.g. CO2. The number of publications on coordination polymers (CP), Metal Organic Frameworks (MOF) or a group of hybrid compounds (organic-inorganic) increased tenfold at the turn of 2005, which proves the growing interest in this field by scientists around the world. MOF diversity in terms of structure, size, geometry, functionality and flexibility of MOF has led to the study of over 20,000 different MOF’s over the past decade. The search for new materials consists of combining molecular building blocks with the desired physicochemical properties. To produce a solid, porous material that can be used in the construction of a "molecular scaffold", rigid organic moieties, which are described in the literature as rods, must be combined with multi-core, inelastic inorganic clusters that act as joints (also called SBU secondary building units). By design, multi-core cluster nodes are able to impart thermodynamic stability through strong covalent bonds and mechanical stability due to coordination bonds that can stabilize the position of metals in the molecule. This property contrasts with those of the unstable single coordination polymers. The size and most importantly the chemical environment of the resulting voids are determined by the length and functions of the organic unit. Therefore, adjusting the appropriate properties of the material is made by appropriate selection of the starting materials. The isoretical method made it possible to use MOF structures with large pores (98 Á and low densities (0.13 g/cm3). This method involves changing the size and nature of Metal Organic Frameworks without changing the topology of their substrate. Thanks to this, it was possible to include large molecules such as vitamins (e.g. B12) or proteins (e.g. green fluorescence protein) into their structure and use the pores as reaction vessels. The thermal and chemical stability of many MOFs has made them amenable to functionalization by post-synthetic covalent organic complexes with metals. These properties make it possible to significantly improve gas storage in MOF structures and have led to their extensive research into the catalysis of organic reactions, activation of small molecules such as hydrogen, methane and water, gas separation, biomedical imaging and conductivity. Currently, methods of producing nanocrystals and MOF super crystals for their incorporation into specialized devices are being developed. Crystalline structures of MOF’s are formed by creating strong bonds between inorganic and organic units. Careful selection of MOF components produces crystals of giant porosity, high thermal and chemical stability. These features allow the interior of the MOF to be chemically altered to separate and store gases. The uniqueness of MOF materials is that they are the only solids to modify and increase the particle size without changing the substrate topology.
Źródło:: Wiadomości Chemiczne; 2021, 75, 7-8; 1041-1073
0043-5104
2300-0295
Pojawia się w:: Wiadomości Chemiczne
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 11.

Tytuł:: Ocena możliwości zastosowania szkieł wodnych sodowych do usuwania najbardziej toksycznych metali: Pb, Hg, Cd z zanieczyszczonych ekosystemów wodnych
Assessment of possibility of using sodium liquid glass for removal of the most toxic metals: Pb, Hg, Cd from contaminated ecosystems
Autorzy:: Koźlak, W.
Powiązania:: https://bibliotekanauki.pl/articles/1287209.pdf
Data publikacji:: 2010
Wydawca:: Stowarzyszenie Inżynierów i Techników Przemysłu Chemicznego. Zakład Wydawniczy CHEMPRESS-SITPChem
Tematy:: szkło wodne sodowe
azotany ołowiu (II)
azotany rtęci (II)
azotany kadmu (II)
badania turbidymetryczne
toksyczność metali
sodium liquid glass
lead (II) nitrates
mercury (II) nitrates
cadmium (II) nitrates
turbidimetric tests
toxicity of metals
Opis:: Scharakteryzowano trzy najbardziej toksyczne metale (Pb, Hg i Cd), uwzględniając ich wpływ na organizmy i środowisko. Zaproponowano metodę turbidymetryczną, polegającą na otrzymywaniu rozpuszczonego koloidalnego krzemianu, dla oceny możliwości wykorzystania szkieł wodnych do usuwania toksycznych metali Pb i Cd z zanieczyszczonych mediów wodnych. Z przebiegu krzywych zmętnienia wynika, że - z wyjątkiem soli Hg (II) - we wszystkich przypadkach wartości zmętnienia w układach z jonami Pb2+ rosną w czasie, natomiast krzemian kadmu powstaje natychmiast w czasie t = 0 i nie ma dalszego przyrostu zmętnienia w czasie. Charakter krzywych zmętnienia związany jest z rodzajem krzemianu tj. jego modułem krzemianowym. Stwierdzono, że szkła wodne sodowe można zastosować do oczyszczania mediów wodnych z najbardziej toksycznych pierwiastków (Pb i Cd). W przypadku soli rtęci (II) proponowana metoda jest zawodna.
Three most toxic metals (Pb, Hg and Cd) were characterized, considering their impact on organisms and environment. Turbidimetric method that consists in obtaining of dissolved colloidal silicate for assessment of possibility of using liquid glasses for removal of toxic metals Pb and Cd from contaminated water media has been suggested. From time process of turbidity curves it results that, with exclusion of Hg (II) salts - in the systems with Pb2+ ions, in all cases turbidity values increase in time, but cadmium silicate is forming instantly in time t=0 and there is no further increase of turbidity in time. Character of turbidity curves is associated with type of silicate i.e. its silicate module. It was found that sodium liquid glasses can be used to remove most toxic elements (Pb and Cd) from water media. In the case of mercury (II) salts, the suggested method is fallible.
Źródło:: Chemik; 2010, 64, 6; 452-461
0009-2886
Pojawia się w:: Chemik
Dostawca treści:: Biblioteka Nauki

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