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Tytuł:
Effect of Mg Ratio on the Extraction of Dy from (Nd,Dy)-Fe-B Permanent Magnet Using Liquid Mg
Autorzy:
Park, Sang-Min
Nam, Sun-Woo
Cho, Ju-Young
Lee, Sang-Hoon
Hyun, Seung-Keun
Kim, Taek-Soo
Powiązania:
https://bibliotekanauki.pl/articles/353657.pdf
Data publikacji:
2020
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
dysprosium
liquid metal extraction
(Nd,Dy)-Fe-B magnet
extraction behavior
diffusion
Opis:
Recently, since the demand of rare earth permanent magnet for high temperature applications such as an electric motor has increased, dysprosium (Dy), a heavy rare earth element, is becoming important due to severe bias in its production. To fulfillthe increasing need of Dy, recycling offers as a promising alternative. In recycling of rare earths, Hydro-metallurgical extraction method is mainly used however it has adverse environmental effects. Liquid metal extraction on the other hand, is an eco-friendly and simple method as far as the reduction of rare earth metal oxide is concerned. Therefore, liquid metal extraction was studied in this research as an alternative to the hydro-metallurgical recycling method. Magnesium (Mg) is selected as solvent metal because it doesn’t form intermetallic compounds with Fe, B and has a low melting and low boiling point. Extraction behavior of Dy in (Nd,Dy)-Fe-B magnet is observed and effect of Mg ratio on extraction of Dy is confirmed.
Źródło:
Archives of Metallurgy and Materials; 2020, 65, 4; 1281-1285
1733-3490
Pojawia się w:
Archives of Metallurgy and Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Phase Evolution During Extraction and Recovery of Pure Nd from Magnet
Autorzy:
Rasheed, Mohammad Zarar
Nam, Sun-Woo
Lee, Sang-Hoon
Park, Sang-Min
Cho, Ju-Young
Kim, Taek-Soo
Powiązania:
https://bibliotekanauki.pl/articles/2048880.pdf
Data publikacji:
2021
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
Liquid Metal Extraction
rare earth recycling
vacuum distillation
phase transformation
Opis:
Liquid Metal Extraction process using molten Mg was carried out to obtain Nd-Mg alloys from Nd based permanent magnets at 900°C for 24 h. with a magnet to magnesium mass ratio of 1:10. Nd was successfully extracted from magnet into Mg resulting in ~4 wt.% Nd-Mg alloy. Nd was recovered from the obtained Nd-Mg alloys based on the difference in their vapor pressures using vacuum distillation. Vacuum distillation experiments were carried out at 800°C under vacuum of 2.67 Pa at various times for the recovery of high purity Nd. Nd having a purity of more than 99% was recovered at distillation time of 120 min and above. The phase transformations of the Nd-Mg alloy during the process, from Mg12Nd to α-Nd, were confirmed as per the phase diagram at different distillation times. Pure Nd was recovered as a result of two step recycling process; Liquid Metal Extraction followed by Vacuum Distillation.
Źródło:
Archives of Metallurgy and Materials; 2021, 66, 4; 1001-1005
1733-3490
Pojawia się w:
Archives of Metallurgy and Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Effect of Magnet Scrap Size on the Extraction Behavior of Heavy Rare Earth Elements by Liquid Metal Extraction
Autorzy:
Nam, Sun-Woo
Rasheed, Mohammad Zarar
Park, Sang-Min
Lee, Sang-Hoon
Kim, Do-Hyang
Kim, Taek-Soo
Powiązania:
https://bibliotekanauki.pl/articles/355705.pdf
Data publikacji:
2020
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
liquid metal extraction
rare earth elements
recycling
oxidation
magnet scrap
Opis:
Liquid metal extraction (LME) process results in 100% neodymium (Nd) extraction but the highest extraction efficiency reportedfor Dysprosium (Dy) so far is 74%. Oxidation of Dy is the major limiting factor for incomplete Dy extraction. In order to enhance the extraction efficiency and to further investigate the limiting factors for incomplete extraction, experiments were carried out on six different particle sizes of under 200 μm, 200-300 μm, 300-700 μm, 700-1000 μm, 1000-2000 μm and over 2000 μm at 900°C with magnesium-to-magnet scrap ratio of 15:1 for 6, 24 and 48 hours, respectively. This research identified Dy2 Fe17 in addition toDy2 O3 phase to be responsible for incomplete extraction. The relationship between Dy2 Fe17 and Dy2O3 phase was investigated, and the overall extraction efficiency of Dy was enhanced to 97%.
Źródło:
Archives of Metallurgy and Materials; 2020, 65, 4; 1273-1276
1733-3490
Pojawia się w:
Archives of Metallurgy and Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Aminated PVC cross-linked with 2,2’-dichlorodiethyl ether as heavy metal absorber
Aminowany PVC sieciowany za pomocą eteru 2,2’-dichlorodietylowego jako absorber metali ciężkich
Autorzy:
Mabrouki, Adnen
Bouzayene, Faycel
Awatef, Soltani
Ammari, Fayçel
Powiązania:
https://bibliotekanauki.pl/articles/2202595.pdf
Data publikacji:
2022
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Chemii Przemysłowej
Tematy:
poly(vinyl chloride)
metal extraction
diethylenetriamine
dichlorodiethyl ether
poli(chlorek winylu)
ekstrakcja metali
dietylenotriamina
eter dichlorodietylowy
Opis:
The paper describes the chemical modification of PVC consisting in the introduction of amino groups (1,4-dioxane, diethylenetriamine), and then cross-linking with dichlorodiethyl ether. The optimal extraction time was obtained for the polymer that had more chlorine atoms substituted with diethylenetriamine groups and ether. The obtained polymers were characterized by infrared spectroscopy (FTIR), elemental analysis (CHN) and differential thermal analysis (DTA).
W pracy opisano chemiczną modyfikację PVC polegającą na wprowadzeniu grup aminowych (1,4-dioksan, dietylenotriamina), a następnie sieciowaniu eterem dichlorodietylowym. Optymalny czas ekstrakcji uzyskano w przypadku polimeru, który miał więcej atomów chloru podstawionych grupami dietylenotriaminowymi i eterem. Otrzymane polimery scharakteryzowano za pomocą spektroskopii w podczerwieni (FTIR), analizy elementarnej (CHN) oraz różnicowej analizy termicznej (DTA).
Źródło:
Polimery; 2022, 67, 11-12; 602--608
0032-2725
Pojawia się w:
Polimery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
4-amine-2-mercaptopyrimidine modified silica gel applied in Cd(II) and Pb(II) extraction from an aqueous medium
Autorzy:
Pereira, A.S.
Ferreira, G.
Caetano, L.
Castro, R.S.D.
dos Santos, A.
Padilha, P.M.
Castro, G.R.
Powiązania:
https://bibliotekanauki.pl/articles/778413.pdf
Data publikacji:
2010
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
4-amino-2-merkaptopirymidyna
krzemionka
ekstrakcja metali
środowisko wodne
4-amine-2-mercaptopyrimidine
silica
metal extraction
aqueous medium
Opis:
This paper discusses silica surface modification by a process involving a two-step reaction: anchoring of a silylating agent, followed by an attachment of a 4-amino-2-mercaptopyrimidine molecule. The modified material (Si-BP) was successfully characterized by the FTIR spectra, which revealed amine absorption bands, and through 13C and 29Si NMR spectra, which confirm the proposed structure of the modified silica (Si-BP). Si-BP was used to extract cadmium and lead from an aqueous medium at 298 K. The Si-BP kinetics towards metal ions was very fast, i.e., about 10 minutes, although extraction was significantly impaired at pH 3. The series of adsorption isotherms were adjusted to a modified Langmuir equation and the maximum extraction capacity was 0.193 and 0.387 mmol g-1 for Cd(II) and Pb(II), respectively. An analysis of the Ř values lead to the inference that the resulting metal ligand complex was type 1:1.
Źródło:
Polish Journal of Chemical Technology; 2010, 12, 1; 7-11
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Functional groups grafted on poly(vinyl chloride) – evaluation of new modified polymers in metal ions adsorption
Szczepienie funkcyjnych grup aminowych na poli(chlorku winylu) – ocena przydatności otrzymanych polimerów w adsorpcji jonów metali
Autorzy:
Mbarki, F.
Ammari, F.
Amor, A. B. H.
Meganem, F.
Powiązania:
https://bibliotekanauki.pl/articles/946993.pdf
Data publikacji:
2017
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Chemii Przemysłowej
Tematy:
poly(vinyl chloride)
benzylamine
diethylenetriamine
dichlorodiethyl ether
substitution reaction
metal extraction
poli(chlorek winylu)
benzyloamina
dietylenotriamina
eter dichlorodietylowy
reakcja podstawienia
ekstrakcja jonów metali
Opis:
Poly(vinyl chloride) (PVC) has been subjected to numerous chemical modifications which were undertaken in order to improve its properties, the use of PVC in new applications and understanding of PVC-related phenomena. This work describes the chemical modification of PVC by amino groups (benzylamine and diethylenetriamine) through nucleophilic substitution reactions of its chlorine atoms to obtain P1 polymer. The modified polymer was subsequently reticulated with dichlorodiethyl ether to obtain P2 polymer. The obtained polymers were characterized using infrared spectroscopy (FT-IR), elemental analysis (CHN), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), differential thermal analysis (DTA), and X-ray diffraction (XRD). The modified polymers (P1 and P2) were tested for metal ion extraction (cadmium, cobalt, lead, or chromium) using the solid-phase extraction (SPE) method and the inductively coupled plasma atomic emission spectrometry (ICP-AES) technique. Quantitative adsorption measurements were performed using solutions containing 2 • 10-4M of heavy metal ions with pH = 3.5–4.5 at a flow rate of 0.6 dm3/min. The new extractants based on modified PVC (P1 and P2) were able to remove the negative effects of heavy metals contained in aqueous solutions. For Pb2+, the extraction percentage was 98 % using P1 and 90.3 % using P2.
Przeprowadzono chemiczną modyfikację poli(chlorku winylu) (PVC) w reakcji nukleofilowego podstawienia atomów chloru grupami aminowymi (benzyloamina i dietylenotriamina). Otrzymany polimer P1 szczepiono następnie eterem dichlorodietylowym – uzyskano polimer P2. Wytworzone polimery scharakteryzowano za pomocą spektroskopii w podczerwieni (FT-IR), analizy elementarnej (CHN), różnicowej kalorymetrii skaningowej (DSC), analizy termograwimetrycznej (TGA), różnicowej analizy termicznej (DTA) i dyfrakcji rentgenowskiej (XRD). Polimery P1 i P2 testowano w procesie ekstrakcji jonów metali (kadmu, kobaltu, ołowiu lub chromu), stosując ekstrakcję w fazie stałej (SPE) imetodę atomowej spektrometrii emisyjnej z plazmą wzbudzaną indukcyjnie (ICP-AES). Pomiary ilościowe adsorpcji prowadzono w roztworach wodnych zawierających 2 • 10-4M jonów metali ciężkich, opH=3,5–4,5 i przy szybkości przepływu 0,6 dm3/min. Nowe ekstrahenty na bazie zmodyfikowanego PVC (P1, P2) adsorbowały metale ciężkie zawarte w roztworach wodnych – w wypadku jonów Pb2+ ekstrakcja za pomocą P1 wyniosła 98 %, a za pomocą P2 – 90,3 %.
Źródło:
Polimery; 2017, 62, 2; 109-117
0032-2725
Pojawia się w:
Polimery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Selective solvent extraction of some heavy metal ions from aqueous solutions by octafunctionalized resorcin[4]arenes
Autorzy:
Kończyk, Joanna
Dlugosz, Jan
Powiązania:
https://bibliotekanauki.pl/articles/110830.pdf
Data publikacji:
2020
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
solvent extraction
lead
chromium
calixresorcinarene
metal removal
Opis:
This paper presents the results of the study on the extraction capacity of 1,8,15,22-tetra(1- heptyl)resorcin[4]arene and its octasubstituted derivatives containing thiophosphoryl, ester and amide groups in the presence of Pb(II), Zn(II), Cd(II) and Cr(III) in solvent extraction process. Effects of the structure and concentration of the resorcinarene extractant and the composition of the aqueous phase as well as its acidity on the efficiency and selectivity of removal of the examined metal ions from model aqueous solutions were determined. The 1:1 stoichiometry for complexes formed between Pb(II) and Cr(III) and the octasubstituted resorcin[4]arenes was determined by classical slope analysis and loading test.
Źródło:
Physicochemical Problems of Mineral Processing; 2020, 56, 2; 271-285
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Effect of coexisting sodium ion extractive separation of metal ions with calix[4]arene tetracarboxylic acid
Autorzy:
Ohto, K.
Shioya, A.
Higuchi, H.
Oshima, T.
Inoue, K.
Powiązania:
https://bibliotekanauki.pl/articles/346949.pdf
Data publikacji:
2002
Wydawca:
Politechnika Bydgoska im. Jana i Jędrzeja Śniadeckich. Wydział Technologii i Inżynierii Chemicznej
Tematy:
calix[4]arene
metal separation
solvent extraction
coexisting sodium ion
Opis:
Solvent extraction of metal ions with calix[4]arene tetracarboxylic acid has been carried out to elucidate effect of coexisting sodium ion. Extraction of metal ions examined, Pb(II), Fe(III), Cu(II), Zn(II), Ni(II), and Co(II), is enhanced by the addition of sodium ion. The enhancement degree of the metal extraction is not necessarily in proportion to the added sodium concentration. The addition of trace amount of sodium ion is necessary to specifically complex for calix[4]arene tetracarboxylic acid and to enhance the extraction ability. However, the addition of excessive amounts of sodium suppresses the extraction of other metal ions, since they act as a competitive ion with other metal ions; The relation between extractive pH1/2 of metal ions and sodium concentration is shown. Mutual separation of metal ions by using additional sodium ion is also investigated. Although complete mutual separation of three metal ions, Pb(II), Cu(II), and Zn(II), has not been achieved, the possibility that the sodium addition will enhance not only the extraction ability but also the separation efficiency is suggested.
Źródło:
Ars Separatoria Acta; 2002, 1; 61-70
1731-6340
Pojawia się w:
Ars Separatoria Acta
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Separation of Co(II), Cu(II), Ni(II) and Mn(II) from synthetic hydrochloric acid leaching solution of spent lithium ion batteries by solvent extraction
Autorzy:
Nguyen, Viet Nhan Hoa
Lee, Man Seung
Powiązania:
https://bibliotekanauki.pl/articles/1449331.pdf
Data publikacji:
2020
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
spent lithium-ion batteries
divalent metal ions
solvent extraction
separation
Opis:
Spent lithium ion batteries contain valuable critical metals such as cobalt, copper, lithium and nickel. In order to develop a process for the separation of the divalent metal ions from spent lithium ion batteries, solvent extraction experiments were performed by employing synthetic hydrochloric acid leaching solution. The synthetic solution contained Cu(II), Co(II), Mn(II) and Ni(II) and its acidity was 3 M HCl. Extraction with Aliquat 336 led to selective extraction of Cu(II) with a small amount of Co(II). After adding NaCl to the Cu(II) free raffinate to enhance the complex formation of Co(II), Co(II) was selectively extracted into Aliquat 336 together with Mn(II). The small amount of Mn(II) in the loaded Aliquat 336 was scrubbed by pure Co(II) solution. After adjusting the pH of the raffinate to 3, 91,3% of Mn(II) was selectively extracted over Ni(II) by the mixture of D2EHPA and Alamine 336. In this extraction, the mole fraction of D2EHPA in the mixture affected the extraction of Mn(II). McCabe-Thiele diagrams for the extraction of Cu(II) and Co(II) were constructed. Batch simulation experiments for the three stage counter-current extraction verified the selective extraction of the target metal ions in each extraction step. Namely, the total extraction percentage of Cu(II) and Co(II) was 71.6% and 98.8% respectively. Most metals in the loaded organic phase were stripped completely with the appropriate agents (1.0 M $H_2SO_4$ for Cu(II), 0.1 M H2SO4 for Co(II) and 0.3 M $HCl$ for Mn(II) stripping). A process was proposed to separate the metal ions by solvent extraction.
Źródło:
Physicochemical Problems of Mineral Processing; 2020, 56, 4; 599-610
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Solvent extraction of copper(II) from chloride solutions using 1,1′-dialkyl-2,2′ bibenzimidazoles as extractants
Autorzy:
Mądrzak-Litwa, Iwona
Borowiak-Resterna, Aleksandra
Powiązania:
https://bibliotekanauki.pl/articles/110851.pdf
Data publikacji:
2019
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
copper
solvent extraction
metal removal
chloride solution
2,2′-bibenzimidazole
Opis:
The solvent extraction ability of 1,1′-dialkyl-2,2′-bibenzimidazoles (L) for the recovery of copper(II) ions from aqueous chloride solutions has been investigated. It was found that 1,1′-didecyl- 2,2′-bibenzimidazole is a useful extractant for the separation of copper(II) ions from both weakly and strongly acidic solutions. Copper(II) can be effectively stripped of organic solutions by a water or ammonia solution in a one-stage process. In low acidity media (pH feed > 1), the extraction percentage of Cu(II) increases with an increase in metal ions and chloride concentrations. Copper(II) ions are extracted as binuclear complexes (CuCl2) 2L2 (L = extractant). The constructed McCabe−Thiele diagram shows that the reduction of copper(II) ions concentration from 25 to approximately 5 g/dm3 in an aqueous feed is possible in two extraction stages. When [HCl] feed ≥ 1 M, (LH+)2(CuCl 4 2)L complex is formed. From the strongly acidic solutions ([HCl] = [LiCl] = 4 M), almost 100% of copper(II) ions can be removed by 1,1′-didecyl-2,2′-bibenzimidazole. Benzyl alcohol, used as an organic phase modifier, enables the selective extraction of copper(II) over zinc(II) ions from a weakly acidic chloride solution.
Źródło:
Physicochemical Problems of Mineral Processing; 2019, 55, 5; 1165-1178
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Quantitative and qualitative analysis of slags from zinc and lead metallurgy
Autorzy:
Nocoń, Milena
Korus, Irena
Loska, Krzysztof
Powiązania:
https://bibliotekanauki.pl/articles/27311569.pdf
Data publikacji:
2023
Wydawca:
Polska Akademia Nauk. Czasopisma i Monografie PAN
Tematy:
heavy metal slags
BCR sequential extraction
zinc and lead metallurgy
AAS
Opis:
The zinc and lead industry generates substantial quantities of waste. Among the many types of wastes, such as dust or liquid, a large proportion are solid waste such as slags. The purpose of the study was the qualitative and quantitative assessment of the short rotary kiln slags and slags deposited in a hazardous waste landfill originating from zinc and lead metallurgy. This assessment represents the primary step in evaluating materials such as slags concerning their potential for substantial applications, such as process for metal separation. Additionally, this evaluation forms the basis for a comprehensive environmental study. The concentrations of the four predominant metals – Fe>Pb>Zn>Cu – and accompanying elements – Na>Ca>K>Ni>Mn>Cr – were determined using atomic absorption spectroscopy (AAS) after aqua regia digestion. A large variation was found in the phase analysis of the studied materials based on SEM, XRD, X-ray microanalysis, and BCR sequential extraction. The BCR analysis revealed the occurrence of major metals in four different fractions: acid-soluble, reducible, oxidizable, and residual. Pb was mainly present in the acid-soluble fraction, while Fe, Cu, and Zn were present in the residual fraction.
Źródło:
Archives of Environmental Protection; 2023, 49, 3; 26--37
2083-4772
2083-4810
Pojawia się w:
Archives of Environmental Protection
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Profile differentiation of lead and chromium fractions found in soils localized on a moraine slope
Profilowe zróżnicowanie zawartości frakcji ołowiu i chromu w glebach położonych na stoku morenowym
Autorzy:
Kalembasa, D.
Majchrowska-Safaryan, A.
Pakula, K.
Powiązania:
https://bibliotekanauki.pl/articles/15503.pdf
Data publikacji:
2009
Wydawca:
Uniwersytet Warmińsko-Mazurski w Olsztynie / Polskie Towarzystwo Magnezologiczne im. Prof. Juliana Aleksandrowicza
Tematy:
chromium
lead
moraine slope
sequential extraction
soil
soil environment
heavy metal
fraction
determination
fractionation method
metal content
Opis:
In order to evaluate a potential threat to soil environment by heavy metals, it is important to separate and determine their fractions by means of sequential extraction. The research aimed at evaluating the total content of lead and chromium as well as their fractions in soils localized on a moraine slope in the Siedlce Heights (transects A and B). Sequential fractionation of these elements was carried out according to Zeien and Brümmer’s method. Chemical analyses revealed varied contents of seven lead and chromium fractions in the soils. The largest amounts of both heavy metals were mostly recorded in the residual fraction (F7), and those of lead also in the organic fraction (F4). The least lead was found in the exchangeable fraction (F2) (it was not detected in easily soluble fraction F1), while the least chromium appeared in the easily soluble (F1) and organic fractions (F4). Statistical processing revealed that the examined lead and chromium fractions generally depended on separated fractions, total contents of these metals, and some properties of analyzed soils.
Dla oceny potencjalnego zagrożenia środowiska glebowego przez metale ciężkie istotne jest wydzielenie i ilościowe zbadanie ich frakcji na drodze ekstrakcji sekwencyjnej. Celem pracy by³o zbadanie ogólnej zawartości ołowiu i chromu oraz ich frakcji w glebach położonych na stoku morenowym Wysoczyzny Siedleckiej (transekt A i B). Frakcjonowanie sekwencyjne tych pierwiastków przeprowadzono według metody Zeiena i Brümmera. Wykazano zróżnicowaną zawartość wydzielonych siedmiu frakcji ołowiu i chromu w badanych glebach. Najwięcej obydwu metali stwierdzono (w przeważającej większości) we frakcji rezydualnej F7, a najwięcej ołowiu we frakcji organicznej (F4). Najmniej ołowiu stwierdzono we frakcji wymiennej F2 (we frakcji łatwo rozpuszczalnej F1 nie został on wykryty), a najmniej chromu we frakcji łatwo rozpuszczalnej (F1) oraz organicznej (F4). Obliczenia statystyczne wykazały, że badane frakcje ołowiu i chromu były przeważnie istotnie zależne od wydzielonych frakcji, ogólnej zawartości tych metali oraz niektórych właściwości analizowanych gleb.
Źródło:
Journal of Elementology; 2009, 14, 4
1644-2296
Pojawia się w:
Journal of Elementology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Sequential extraction of carbonaceous siltstone rock for multielement analysis by ICP OES
Autorzy:
Junussov, M.
Mádai, F.
Olivér, B.
Powiązania:
https://bibliotekanauki.pl/articles/100814.pdf
Data publikacji:
2018
Wydawca:
Uniwersytet Śląski. Wydział Nauk o Ziemi
Tematy:
sequential extraction
carbonaceous siltstone rock
heavy metal
colloidal gold
ekstrakcja sekwencyjna
metale ciężkie
złoże
złoto koloidalne
Opis:
The carbonaceous siltstone rock material is a disseminated sulfide-rich sedimentary rock from a sedimenthosted gold deposit of Bakyrchik. The Bakyrchik deposit is located in Eastern Kazakhstan, which includes in Qalba gold province. The main purpose of this paper is a demonstration on chemical extraction of heavy metals from the carbonaceous siltstone rock and detection of its elemental concentrations. In the work was used a rock sample from the deposit which is a sericizited carbonaceous-siltstone rock. In sequential extraction method was selected four stages such as water soluble fraction (reaction with deionized water) for extraction of water soluble metals, reducible metal fraction (reaction with hydroxyl ammonium chloride) for extracting all reducible metals, organics and sulfides (reaction with hydrogen peroxide) for dissolution of organics and copper sulfide, and extraction of metal oxides and residual fraction (reaction with aqua regia) for extracting of all remaining metals. The paper comprises analytical methods for research outlooks. They are X-Ray Diffraction (determination of mineralogical composition), X-Ray Fluorescence (determination of chemical composition) and Inductively Coupled Plasma - Optical Emission Spectrometry (determination of heavy metal concentrations).
Źródło:
Contemporary Trends in Geoscience; 2018, 7, 2; 145-152
2299-8179
Pojawia się w:
Contemporary Trends in Geoscience
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Quantitative relations between the content of selected trace elements in soil extracted with 0.03 M CH3COOH or 1 M HCL and its total concentration in carrot storage roots
Relacje ilościowe między zawartością wybranych pierwiastków śladowych w glebie ekstrahowanych 0,03 M CH3COOH i 1 M HCL a zawartością ich form ogólnych w korzeniach spichrzowych marchwi
Autorzy:
Smoleń, S.
Sady, W.
Ledwożyw-Smoleń, I.
Powiązania:
https://bibliotekanauki.pl/articles/11541915.pdf
Data publikacji:
2010
Wydawca:
Uniwersytet Przyrodniczy w Lublinie. Wydawnictwo Uniwersytetu Przyrodniczego w Lublinie
Tematy:
soil
chemical composition
extraction
heavy metal
trace element
element concentration
carrot
root
storage
acetic acid
hydrochloric acid
Opis:
There is an existing need for the development of rapid and easy-to-perform methods for analyzing chemical composition of soil basing on simultaneous extraction of many elements in a single solution. Furthermore, it is desirable that mineral concentration determined in soil using these methods should be significantly correlated with its content in plants. Many researches indicated that soil concentration of heavy metals and trace elements after extraction using 0.01 M CaCl2 did not reflect its content in vegetable plants.. The aim of the research was to determine the relation between soil content of: Al, B, Ba, Cd, Co, Cr, Cu, Fe, Li, Mn, Mo, Ni, Pb, Sr, Ti, V and Zn extracted in 0.03 M CH3COOH as well as 1 M HCl and its content in carrot storage roots. In 2008–2009 studies were carried out on soil samples after carrot cultivation (from 0–30 cm, 30–60 cm and 60–90 cm layers) as well as on carrot storage roots grown on the same soil site. In total, analysis of chemical composition (with respect to the content of tested elements) comprised: 112 samples of carrot storage roots, 112 soil samples from 0–30 cm layer as well as 48 soil samples from 30–60 cm and 60–90 cm layers. Higher applicability of soil extraction with 0.03 M CH3COOH (commonly used for macro element chlorides and boron determination) in comparison to extraction with 1 M HCl was demonstrated in reference to the estimation of the relation between soil and carrot content of: Al, B, Ba, Cd, Cr, Cu, Li, Ni, Sr, Ti and Zn. Application of 1 M HCl gave relatively better results when compared to the extraction with 0.03 M CH3COOH with respect to calculated values of correlation coefficient for Co, Fe, Mn, Mo and Pb content in soil and carrot. Content of Co, Mo, Pb and V in soil after extraction using 0.03 M CH3COOH was below the limits of its detection using ICP-OES spectrometer. No relation was found between vanadium content in soil (analyzed after extraction with 1 M HCl) and its content in carrot storage roots.
Istnieje potrzeba poszukiwania szybkich i łatwych do wykonania metod analizy zawartości składników w glebach, opartych na wspólnej ekstrakcji wielu składników. Zawartość składników oznaczona w glebach za pomocą tych metod korelowała z ich zawartością w roślinach. Liczne badania wykazały, że zawartość mikroelementów, metali ciężkich oraz pierwiastków śladowych w glebie oznaczana za pomocą 0.01 M CaCl2 nie odzwierciedla zawartości tych składników w warzywach. Celem badań było określenie zależności pomiędzy zawartością w glebie Al, B, Ba, Cd, Co, Cr, Cu, Fe, Li, Mn, Mo, Ni, Pb, Sr, Ti, V i Zn ekstrahowanych za pomocą 0,03 M CH3COOH i 1 M HCl, a ich zawartością w korzeniach spichrzowych marchwi. W latach 2008–2009 badaniami objęto próby gleby (z warstw 0–30 cm, 30–60 cm i 60–90 cm) po uprawie marchwi oraz próby korzeni spichrzowych marchwi z uprawy polowej prowadzonej na tym samym stanowisku glebowym. Łącznie analizie składu chemicznego (pod względem zawartości badanych pierwiastków) poddano 112 prób korzeni spichrzowych marchwi i 112 prób gleby z warstwy 0–30 cm oraz po 48 prób gleby z warstw 30–60 cm i 60–90 cm. Badania wykazały większą przydatność ekstrakcji gleby 0,03 M CH3COOH (standardowo służącej do określania zawartości makroskładników chlorków i boru) niż ekstrakcji 1 M HCl do oceny związku pomiędzy zawartością Al, B, Ba, Cd, Cr, Cu, Li, Ni, Sr, Ti i Zn w glebie a zawartością tych pierwiastków w korzeniach spichrzowych marchwi. Zastosowanie ekstrakcji 1 M HCl dało stosunkowo lepsze rezultaty niż ekstrakcja 0,03 M CH3COOH w zakresie wielkości współczynników korelacji pomiędzy zawartością Co, Fe, Mn, Mo i Pb w glebie i marchwi. Zawartość Co, Mo, Pb i V w glebie po ekstrakcji 0,03 M CH3COOH była niższa od limitu detekcji spektrometru ICP-OES. Nie wykazano związku pomiędzy zawartością wanadu w glebie (oznaczanego w 1 M HCl) a zawartością V w korzeniach spichrzowych marchwi.
Źródło:
Acta Scientiarum Polonorum. Hortorum Cultus; 2010, 09, 4; 3-12
1644-0692
Pojawia się w:
Acta Scientiarum Polonorum. Hortorum Cultus
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Solvent Extraction of Metal Ions from Sulfate Solutions Obtained in Leaching of Spent Ni-MH Batteries
Autorzy:
Pośpiech, Beata
Gęga, Jerzy
Powiązania:
https://bibliotekanauki.pl/articles/27315799.pdf
Data publikacji:
2019
Wydawca:
STE GROUP
Tematy:
solvent extraction
rare earth metals
nickel metal hydride batteries
ekstrakcja rozpuszczalnikiem
metale ziem rzadkich
akumulatory niklowo-wodorkowe
Opis:
The nickel metal hydride batteries (Ni-MH) are used in many electronic equipment, like cell phones, computers, cameras as well as hybrid cars. Spent batteries can be a rich source of many metals, especially rare earth elements (REE), such as lanthanum (La), cerium (Ce), neodymium (Nd), praseodymium (Pr), samarium (Sm), gadolinium (Gd). Ni-MH batteries also contain iron (Fe) as well as non-ferrous metals, i.e. nickel (Ni), cobalt (Co), zinc (Zn), manganese (Mn), etc. Leaching of such waste with sulfuric acid solutions is one among many methods recovering of useful metals in hydrometallurgical processes. The main aim of this work was separation of metal ions from pregnant leach liquor (PLL) by solvent extraction using phosphorous compounds and ionic liquids (ILs). The initial pH of the aqueous solution was 0.1. Di (2-ethylhexyl) phosphoric acid (D2EHPA), bis (2,2,4-trimethylpentyl) phosphinic acid (Cyanex 272), and phosphoniumionic liquid - trihexyl (tetradecyl) phosphonium bis (2,4,4- trimethylpentyl) phosphinate (Cyphos IL 104) were used as the selective extractants. The initial concentration of the extractants in an organic phase was equal to 0.1 mol dm-3. The obtained results show that the highest extraction efficiency was obtained for Fe(III) and Zn(II) in extraction experiments with 0.1 M D2EHPA at pH of 0.1. Ni(II), Co(II) and REE remained in the aqueous solutions. In the next stage, REE were extracted with the mixture of 0.1 M Cyanex 272 and 0.1 M Cyphos IL 104 at pH equal to 3.8. Finally, Ni(II) and Co(II) ions were efficiently removed from the aqueous phase using 0.1 M solution of Cyphos IL 104 at pH around 5.4.
Źródło:
New Trends in Production Engineering; 2019, 2, 2; 214-221
2545-2843
Pojawia się w:
New Trends in Production Engineering
Dostawca treści:
Biblioteka Nauki
Artykuł
Wyświetlanie 1-15 z 23

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