kth.sePublikationer
Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Selective Separation of Metal Ions by Solvent Extraction, Liquid Membranes and Magnetic Nanoparticles
KTH, Skolan för industriell teknik och management (ITM), Materialvetenskap.ORCID-id: 0000-0001-6288-7709
2006 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Ort, förlag, år, upplaga, sidor
Stockholm: KTH , 2006. , s. xvi, 50
Nyckelord [en]
solvent extraction, facilitated transport, Pt(IV), Pd(II), Ph(III), permeation medelling, thermodynamic modelling
Nationell ämneskategori
Materialkemi
Identifikatorer
URN: urn:nbn:se:kth:diva-3871ISBN: 91-7178-281-8 (tryckt)OAI: oai:DiVA.org:kth-3871DiVA, id: diva2:9819
Disputation
2006-03-17, Salongen, KTHB, Osquars backe 31, Stockholm, 10:00
Opponent
Handledare
Anmärkning

QC 20100924

Tillgänglig från: 2006-03-08 Skapad: 2006-03-08 Senast uppdaterad: 2022-10-24Bibliografiskt granskad
Delarbeten
1. Selective extraction of palladium(II) from chloride solutions with nonylthiourea dissolved in chloroform
Öppna denna publikation i ny flik eller fönster >>Selective extraction of palladium(II) from chloride solutions with nonylthiourea dissolved in chloroform
2002 (Engelska)Ingår i: Solvent extraction and ion exchange, ISSN 0736-6299, E-ISSN 1532-2262, Vol. 20, nr 6, s. 717-733Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The extraction of Palladium(II) [Pd(II)] from hydrochloric acid solutions with nonylthiourea (NTH) dissolved in chloroform at a constant ionic strength of LOM has been studied. The extraction of Pd(II) has been investigated as a function of the concentration of the extractant, chloride ion, and proton concentrations as well as extraction temperature. The distribution data have been treated graphically and numerically. The analysis of the experimental data has shown that Pd(II) is extracted as PdCl2 . (NTH) and PdCl2 . (NTH)(2) species with the respective extraction constants of log K-11 = 5.0 +/- 0.1 and log K-12 = 9.1 +/- 0.1. The back-extraction of Pd(II) from the organic phase using different stripping reagents has been examined. The selectivity of NTH for Pd(II) against Pt(IV), Rb(III), Cu(II), Fe(III), and Zn(II) has also been investigated.

Nyckelord
liquid-liquid-extraction, solvent-extraction, hydrochloric-acid, platinum metals, noble-metals, sulfide, gold, separation, thiourea, reagents
Nationell ämneskategori
Materialkemi
Identifikatorer
urn:nbn:se:kth:diva-22108 (URN)10.1081/sei-120016075 (DOI)000179678100006 ()2-s2.0-0036875673 (Scopus ID)
Anmärkning
QC 20100525Tillgänglig från: 2010-08-10 Skapad: 2010-08-10 Senast uppdaterad: 2022-10-24Bibliografiskt granskad
2. Extraction of platinum(IV) with nonylthiourea dissolved in chloroform from hydrochloric acid media
Öppna denna publikation i ny flik eller fönster >>Extraction of platinum(IV) with nonylthiourea dissolved in chloroform from hydrochloric acid media
2003 (Engelska)Ingår i: Solvent extraction and ion exchange, ISSN 0736-6299, E-ISSN 1532-2262, Vol. 21, nr 6, s. 827-840Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The extractant nonylthiourea (NTH) in chloroform has been investigated for the extraction of Pt(IV) from chloride solutions at ionic strength of I = 4.0 M and at 22degreesC. It has been found that chloride concentration has a negative effect on the extraction equilibrium, while proton concentration has no effect. The numerical analysis of the equilibrium data has shown that the extraction of PtCl62- with NTH can be interpreted by the formation Of PtCl4(NTH) and PtCl4(NTH)(4) species with their respective equilibrium constants of log K-11 = 5.06 +/- 0.01 and log K-14 = 14.12 +/- 0.04 in 4 M HCl. FTIR spectra of the free NTH and the NTH-Pt(IV) complex were studied to obtain some information on the interaction between Pt(IV) ions and NTH molecules.

Nyckelord
di-ortho-tolylthiourea, solvent-extraction, group-metals, gold, complexes, thiourea, diphenylthiourea, derivatives, separation, palladium
Nationell ämneskategori
Materialkemi
Identifikatorer
urn:nbn:se:kth:diva-22981 (URN)10.1081/sei-120025927 (DOI)000186740800004 ()2-s2.0-0347517471 (Scopus ID)
Anmärkning
QC 20100525Tillgänglig från: 2010-08-10 Skapad: 2010-08-10 Senast uppdaterad: 2022-10-24Bibliografiskt granskad
3. Thermodynamic modeling of extraction equilibria of platinum and palladium with nonylthiourea from hydrochloric acid media
Öppna denna publikation i ny flik eller fönster >>Thermodynamic modeling of extraction equilibria of platinum and palladium with nonylthiourea from hydrochloric acid media
2004 (Engelska)Ingår i: Separation science and technology (Print), ISSN 0149-6395, E-ISSN 1520-5754, Vol. 39, nr 15, s. 3665-3677Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Models of extraction equilibria of Pt(IV) and Pd(II) with Nonylthiourea (NTH) from HCl media have been studied. The conditional equilibrium constants and the stoichiometry of the extracted species of Pt(IV) with NTH at different ionic strengths obtained by numerical analysis using the LETAGROP-DISTR program are reported. The dependence of the extraction constant values on the ionic strength has been analysed using the Specific Interaction Theory (SIT), from which the respective thermodynamic equilibrium constants of the extraction of Pt(IV) and Pd(II) with NTH have been determined. The thermodynamic equilibrium constants determined for Pt(IV) are log K-11o=5+/-1 and log K-14(o)=14.6+/-0.2, while for Pd(II) log K-11(o)=4.9+/-0.1 and log K-12(o)=9.17+/-0.08. The interaction coefficients, epsilon, for the pairs (H+, PtCl62-) and (H+, PdCl42-) have also been estimated to be 0.30+/-0.08 and 0.41+/-0.02, respectively.

Nyckelord
platinum, palladium, thermodynamic modeling, aqueous-solutions, electrolytes
Nationell ämneskategori
Materialkemi
Identifikatorer
urn:nbn:se:kth:diva-23916 (URN)10.1081/ss-200039123 (DOI)000225404100012 ()2-s2.0-9144256366 (Scopus ID)
Anmärkning
QC 20100525 QC 20110914Tillgänglig från: 2010-08-10 Skapad: 2010-08-10 Senast uppdaterad: 2022-10-24Bibliografiskt granskad
4. Transport of palladium(II) through hollow fiber supported liquid membrane facilitated by nonylthiourea
Öppna denna publikation i ny flik eller fönster >>Transport of palladium(II) through hollow fiber supported liquid membrane facilitated by nonylthiourea
2004 (Engelska)Ingår i: Journal of Membrane Science, ISSN 0376-7388, E-ISSN 1873-3123, Vol. 241, nr 2, s. 289-295Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The facilitated transport of Pd(II) from chloride media has been investigated through a hollow-fiber supported liquid membrane using nonylthiourea (NTH) as a carrier. The influence of the chemical conditions on the permeability of Pd(II) is reported. A model is presented that describes the transport mechanism, consisting of diffusion through a feed aqueous diffusion layer, a fast interfacial chemical reaction, and diffusion of carrier and its metal complex through the organic membrane. The diffusion resistances through organic membrane (Delta(org)) and through aqueous layer (Delta(aq)), respectively, have been calculated from the proposed model. The permeability of Pd(II) seems to be governed by the diffusion of Pd(II) species through the hollow fiber supported liquid membrane with PdCl2(NTH)(2) as a predominant carrier and PdCl2(NTH)to a lesser extent, though both have similar diffusion coefficients.

Nyckelord
palladium(II) transport, supported liquid membrane, nonylthiourea, sulfur-containing reagents, mass-transfer, thiourea derivatives, mobile carrier, separation, acid, platinum(iv), extraction, mechanism, gold(iii)
Nationell ämneskategori
Materialkemi
Identifikatorer
urn:nbn:se:kth:diva-23683 (URN)10.1016/j.memsci.2004.05.020 (DOI)000223577000013 ()2-s2.0-4043173506 (Scopus ID)
Anmärkning
QC 20100525 QC 20110922Tillgänglig från: 2010-08-10 Skapad: 2010-08-10 Senast uppdaterad: 2022-10-24Bibliografiskt granskad
5. Fe3O4 and gamma-Fe2O3 nanoparticles for the adsorption of Co2+ from aqueous solution
Öppna denna publikation i ny flik eller fönster >>Fe3O4 and gamma-Fe2O3 nanoparticles for the adsorption of Co2+ from aqueous solution
Visa övriga...
2006 (Engelska)Ingår i: Journal of Colloid and Interface Science, ISSN 0021-9797, E-ISSN 1095-7103, Vol. 298, nr 2, s. 501-507Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The adsorption of Co2+ ions from nitrate solutions using iron oxide nanoparticles of magnetite (Fe3O4) and maghemite (gamma-Fe2O3) has been studied. The adsorption of Co2+ ions on the surface of the particles was investigated under different conditions of oxide content, contact time, Solution pH. and initial Co2+ ion concentration. It has been found that the equilibrium can be attained in less than 5 ruin. The maximum loading capacity of Fe3O4 and gamma-Fe2O3 nanoparticles is 5.8 x 10(-5) and 3.7 x 10(-5) mol m(-2), respectively, which are much higher than the previously Studied. iron oxides and conventional ion exchange resins. Co2+ ions were also recovered by dilute nitric acid from the loaded gamma-Fe2O3 and Fe3O4 with an efficiency of 86 and 30%. respectively. That has been explained by the different mechanisms by including both the surface and Structural loadings of Co2+ ions. The Surface adsorption of Co2+ on Fe3O4 and gamma-Fe2O3 nanoparticles has been found to have the same mechanism of ion exchange reaction between Co2+ in the solution and proton bonded on the particle Surface. The conditional equilibrium constants of surface 2-adsorption of Co2+ on Fe3O4 and gamma-Fe-O-2(3) nanoparticles have been determined to be log K = -3.3 +/- 0.3 and -3.1 +/- 0.2, respectively. The Structural loading of Co2+ ions into Fe3O4 lattice has been found to be the ion exchange reaction between CO2+ and Fe2+ while that into gamma-Fe2O3 lattice to fill its vacancy. The effect of temperature on the adsorption of Co2+ was also investigated, and the value of enthalpy change was determined to be 19 kJ mol(-1)

Nyckelord
adsorption, magnetite, maghemite, cobalt(II), nanoparticles, magnetite particles, reaction-kinetics, iron-oxide, ions, hematite, goethite, cadmium, desorption, cobalt(ii), sorption
Nationell ämneskategori
Materialkemi
Identifikatorer
urn:nbn:se:kth:diva-15713 (URN)10.1016/j.jcis.2005.12.057 (DOI)000237909100001 ()16448661 (PubMedID)2-s2.0-33747758390 (Scopus ID)
Anmärkning
QC 20100525Tillgänglig från: 2010-08-05 Skapad: 2010-08-05 Senast uppdaterad: 2022-12-07Bibliografiskt granskad
6. Adsorption Behavior of Platinum Group Metals (Pd, Pt, Rh) onNonylthiourea-Coated Fe3O4 Nanoparticles
Öppna denna publikation i ny flik eller fönster >>Adsorption Behavior of Platinum Group Metals (Pd, Pt, Rh) onNonylthiourea-Coated Fe3O4 Nanoparticles
Visa övriga...
2006 (Engelska)Ingår i: Separation science and technology (Print), ISSN 0149-6395, E-ISSN 1520-5754, Vol. 41, s. 909-923Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Magnetite nanoparticles coated with nonylthiourea (NTH) were synthesizedand analyzed for the separation and recovery of platinum group metals (PGMs) fromdiluted aqueous chloride solutions. Physical characterizations of the coated nanoparticleswere performed by Transmission Electron Microscopy (TEM), ThermogravimetricAnalysis (TGA) and FT-IR Spectrometry. Separation efficiency of the coatednanoparticles and the equilibrium adsorption isotherm of PGMs were investigated.The maximum adsorption was attained in less than 30 minutes, and the maximumloading capacity of NTH-coated Fe3O4 nanoparticles for Pt(IV) and Pd(II) was determinedto be 10.7 and 8.1 mg g21, respectively. The recovery of PGMs from the loadednanoparticles was examined using different eluting solutions, including HNO3,thiourea, and NaClO4.

Nyckelord
Adsorption, platinum group metals, magnetite nanoparticles, nonylthiourea
Nationell ämneskategori
Materialkemi
Identifikatorer
urn:nbn:se:kth:diva-24724 (URN)10.1080/01496390600588952 (DOI)000236741500008 ()2-s2.0-33646365402 (Scopus ID)
Anmärkning
QC 20100923Tillgänglig från: 2010-09-23 Skapad: 2010-09-23 Senast uppdaterad: 2022-10-24Bibliografiskt granskad
7. Sorption of palladium(II), rhodium(III), and platinum(IV) on Fe3O4 nanoparticles
Öppna denna publikation i ny flik eller fönster >>Sorption of palladium(II), rhodium(III), and platinum(IV) on Fe3O4 nanoparticles
Visa övriga...
2006 (Engelska)Ingår i: Journal of Colloid and Interface Science, ISSN 0021-9797, E-ISSN 1095-7103, Vol. 301, nr 2, s. 402-408Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The adsorption of palladium(II), rhodium(III), and platinum(IV) from diluted hydrochloric acid solutions onto Fe3O4 nanoparticles has been investigated. The parameters studied include the contact time and the concentrations of metals and other solutes such as H+ and chloride. The equilibrium time was reached in less than 20 min for all metals. The maximum loading capacity of Fe3O4 nanoparticles for Pd(II), Rh(III), and Pt(IV) was determined to be 0.103, 0.149, and 0.068 mmol g(-1), respectively. A sorption mechanism for Pd(II), Rh(III), and Pt(IV) has been proposed and their conditional adsorption equilibrium constants have been determined to be log K = 1.72, 1.69, and 1.84, respectively. Different compositions of eluting solution were tested for the recovery of Pt(IV), Pd(II), and Rh(III) from Fe3O4 nanoparticles. It was found that 0.5 mol L-1 HNO3 can elute all of the metal ions simultaneously, while 1 mol L-1 NaHSO3 was an effective eluting solution for Rh(III), and 0.5 mol L-1 NaClO4 for Pt(IV). In competitive adsorption, the nanoparticles showed stronger affinity for Rh(III) than for Pd(II) and Pt(IV).

Nyckelord
adsorption, magnetite, platinum group metals, nanoparticles, metal distributions, titanium-dioxide, gamma-alumina, adsorption, preconcentration, complexes, catalysts, resin, ph, speciation
Nationell ämneskategori
Materialkemi
Identifikatorer
urn:nbn:se:kth:diva-15934 (URN)10.1016/j.jcis.2006.05.015 (DOI)000239937700008 ()16780854 (PubMedID)2-s2.0-33746919631 (Scopus ID)
Anmärkning

QC 20100525

Tillgänglig från: 2010-08-05 Skapad: 2010-08-05 Senast uppdaterad: 2022-10-24Bibliografiskt granskad

Open Access i DiVA

Fulltext saknas i DiVA

Sök vidare i DiVA

Av författaren/redaktören
Uheida, Abdusalam
Av organisationen
Materialvetenskap
Materialkemi

Sök vidare utanför DiVA

GoogleGoogle Scholar

isbn
urn-nbn

Altmetricpoäng

isbn
urn-nbn
Totalt: 916 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf