Synthesis of linear alkylbenzene sulphonate intercalated iron(II) iron(III) hydroxide sulphate (green rust) and adsorption of carbon tetrachloride

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Synthesis of linear alkylbenzene sulphonate intercalated iron(II) iron(III) hydroxide sulphate (green rust) and adsorption of carbon tetrachloride. / Ayala Luis, Karina Barbara; Kaldor, D.K.; Bender Koch, Christian; Strobel, Bjarne Westergaard; Hansen, Hans Christian Bruun.

I: Clay Minerals, Bind 42, Nr. 3, 2007, s. 307-317.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ayala Luis, KB, Kaldor, DK, Bender Koch, C, Strobel, BW & Hansen, HCB 2007, 'Synthesis of linear alkylbenzene sulphonate intercalated iron(II) iron(III) hydroxide sulphate (green rust) and adsorption of carbon tetrachloride', Clay Minerals, bind 42, nr. 3, s. 307-317. https://doi.org/10.1180/claymin.2007.042.3.04

APA

Ayala Luis, K. B., Kaldor, D. K., Bender Koch, C., Strobel, B. W., & Hansen, H. C. B. (2007). Synthesis of linear alkylbenzene sulphonate intercalated iron(II) iron(III) hydroxide sulphate (green rust) and adsorption of carbon tetrachloride. Clay Minerals, 42(3), 307-317. https://doi.org/10.1180/claymin.2007.042.3.04

Vancouver

Ayala Luis KB, Kaldor DK, Bender Koch C, Strobel BW, Hansen HCB. Synthesis of linear alkylbenzene sulphonate intercalated iron(II) iron(III) hydroxide sulphate (green rust) and adsorption of carbon tetrachloride. Clay Minerals. 2007;42(3):307-317. https://doi.org/10.1180/claymin.2007.042.3.04

Author

Ayala Luis, Karina Barbara ; Kaldor, D.K. ; Bender Koch, Christian ; Strobel, Bjarne Westergaard ; Hansen, Hans Christian Bruun. / Synthesis of linear alkylbenzene sulphonate intercalated iron(II) iron(III) hydroxide sulphate (green rust) and adsorption of carbon tetrachloride. I: Clay Minerals. 2007 ; Bind 42, Nr. 3. s. 307-317.

Bibtex

@article{e39da630a1c211ddb6ae000ea68e967b,
title = "Synthesis of linear alkylbenzene sulphonate intercalated iron(II) iron(III) hydroxide sulphate (green rust) and adsorption of carbon tetrachloride",
abstract = "Green rusts, GRs, can act as both sorbents and reductants towards selected pollutants. Organo-GRs are expected to combine these properties with a high affinity for hydrophobic substances. A novel organo-GR, GRLAS, was synthesized by incorporating a mixture of linear alkylbenzenesulphonates (LAS) into the interlayer space of synthetic sulphate green rust, GR . M{\"o}ssbauer analysis of GRLAS indicates that the structure of the organo-GR is very similar to SO4 that of the initial GR with regard to the FeII/FeIII ratio and local coordination of Fe atoms. X-ray SO4 diffraction demonstrates that the GRLAS formed was well ordered, although a mixture of surfactant was used for intercalation. The basal spacings of the GRLAS and the kinetics of the ion-exchange process were dependent on the initial surfactant loading; basal spacings of ~2.85 nm were obtained at The ratio LAS solution concentrations >10 mM. LASadsorbed/SO42- desorbed significantly exceeded the stoichiometric ratio of 2 during the initial part of the ion-exchange process (t = 5 h). However, this ratio was reached progressively with time. GR preferentially sorbed LAS homologues with long SO4 alkyl chains over short ones. Carbon tetrachloride was successfully adsorbed into GRLAS. The adsorption isotherm was linear with a distribution coefficient, Kd, of 505 ± 19 litre kg-1 ",
keywords = "Former LIFE faculty, green rust, phyllosilicates, layered double hydroxides, reactivity, carbonates, synthesis, organic contaminants",
author = "{Ayala Luis}, {Karina Barbara} and D.K. Kaldor and {Bender Koch}, Christian and Strobel, {Bjarne Westergaard} and Hansen, {Hans Christian Bruun}",
year = "2007",
doi = "10.1180/claymin.2007.042.3.04",
language = "English",
volume = "42",
pages = "307--317",
journal = "Clay Minerals",
issn = "0009-8558",
publisher = "Mineralogical Society",
number = "3",

}

RIS

TY - JOUR

T1 - Synthesis of linear alkylbenzene sulphonate intercalated iron(II) iron(III) hydroxide sulphate (green rust) and adsorption of carbon tetrachloride

AU - Ayala Luis, Karina Barbara

AU - Kaldor, D.K.

AU - Bender Koch, Christian

AU - Strobel, Bjarne Westergaard

AU - Hansen, Hans Christian Bruun

PY - 2007

Y1 - 2007

N2 - Green rusts, GRs, can act as both sorbents and reductants towards selected pollutants. Organo-GRs are expected to combine these properties with a high affinity for hydrophobic substances. A novel organo-GR, GRLAS, was synthesized by incorporating a mixture of linear alkylbenzenesulphonates (LAS) into the interlayer space of synthetic sulphate green rust, GR . Mössbauer analysis of GRLAS indicates that the structure of the organo-GR is very similar to SO4 that of the initial GR with regard to the FeII/FeIII ratio and local coordination of Fe atoms. X-ray SO4 diffraction demonstrates that the GRLAS formed was well ordered, although a mixture of surfactant was used for intercalation. The basal spacings of the GRLAS and the kinetics of the ion-exchange process were dependent on the initial surfactant loading; basal spacings of ~2.85 nm were obtained at The ratio LAS solution concentrations >10 mM. LASadsorbed/SO42- desorbed significantly exceeded the stoichiometric ratio of 2 during the initial part of the ion-exchange process (t = 5 h). However, this ratio was reached progressively with time. GR preferentially sorbed LAS homologues with long SO4 alkyl chains over short ones. Carbon tetrachloride was successfully adsorbed into GRLAS. The adsorption isotherm was linear with a distribution coefficient, Kd, of 505 ± 19 litre kg-1

AB - Green rusts, GRs, can act as both sorbents and reductants towards selected pollutants. Organo-GRs are expected to combine these properties with a high affinity for hydrophobic substances. A novel organo-GR, GRLAS, was synthesized by incorporating a mixture of linear alkylbenzenesulphonates (LAS) into the interlayer space of synthetic sulphate green rust, GR . Mössbauer analysis of GRLAS indicates that the structure of the organo-GR is very similar to SO4 that of the initial GR with regard to the FeII/FeIII ratio and local coordination of Fe atoms. X-ray SO4 diffraction demonstrates that the GRLAS formed was well ordered, although a mixture of surfactant was used for intercalation. The basal spacings of the GRLAS and the kinetics of the ion-exchange process were dependent on the initial surfactant loading; basal spacings of ~2.85 nm were obtained at The ratio LAS solution concentrations >10 mM. LASadsorbed/SO42- desorbed significantly exceeded the stoichiometric ratio of 2 during the initial part of the ion-exchange process (t = 5 h). However, this ratio was reached progressively with time. GR preferentially sorbed LAS homologues with long SO4 alkyl chains over short ones. Carbon tetrachloride was successfully adsorbed into GRLAS. The adsorption isotherm was linear with a distribution coefficient, Kd, of 505 ± 19 litre kg-1

KW - Former LIFE faculty

KW - green rust

KW - phyllosilicates

KW - layered double hydroxides

KW - reactivity

KW - carbonates

KW - synthesis

KW - organic contaminants

U2 - 10.1180/claymin.2007.042.3.04

DO - 10.1180/claymin.2007.042.3.04

M3 - Journal article

VL - 42

SP - 307

EP - 317

JO - Clay Minerals

JF - Clay Minerals

SN - 0009-8558

IS - 3

ER -

ID: 8081767