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Nanoparticles of WC-Co, WC, Co and Cu of relevance for traffic wear particles – Particle stability and reactivity in synthetic surface water and influence of humic matter

Hedberg, Yolanda, 1985- (author)
Karolinska Institutet,KTH,Yt- och korrosionsvetenskap,KTH Royal Institute of Technology, Sweden; Karolinska Institutet, Sweden
Hedberg, Jonas, 1979- (author)
KTH,Yt- och korrosionsvetenskap,KTH Royal Institute of Technology, Sweden
Isaksson, Sara (author)
KTH,Yt- och korrosionsvetenskap,KTH Royal Institute of Technology, Sweden
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Mei, Nanxuan (author)
KTH,Yt- och korrosionsvetenskap,KTH Royal Institute of Technology, Sweden
Blomberg, Eva, 1961- (author)
RISE,KTH,Yt- och korrosionsvetenskap,SP Technical Research Institute of Sweden, Chemistry, Materials and Surfaces, Sweden,Kemi och material,KTH Royal Institute of Technology, Sweden
Wold, S. (author)
KTH Royal Institute of Technology, Sweden
Odnevall Wallinder, Inger, 1965- (author)
KTH,Yt- och korrosionsvetenskap,KTH Royal Institute of Technology, Sweden
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 (creator_code:org_t)
Elsevier, 2017
2017
English.
In: Environmental Pollution. - : Elsevier. - 0269-7491 .- 1873-6424. ; 224, s. 275-288
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Studded tyres made of tungsten carbide cobalt (WC-Co) are in the Northern countries commonly used during the winter time. Tungsten (W)-containing nano- and micron-sized particles have been detected close to busy roads in several European countries. Other typical traffic wear particles consist of copper (Cu). The aims of this study were to investigate particle stability and transformation/dissolution properties of nanoparticles (NPs) of WC-Co compared with NPs of tungsten carbide (WC), cobalt (Co), and Cu. Their physicochemical characteristics (primarily surface oxide and charge) are compared with their extent of sedimentation and metal release in synthetic surface water (SW) with and without two different model organic molecules, 2,3- and 3,4-dihydroxybenzoic acid (DHBA) mimicking certain sorption sites of humic substances, for time periods up to 22 days. The WC-Co NPs possessed a higher electrochemical and chemical reactivity in SW with and without DHBA molecules as compared with NPs of WC, Co, and Cu. Co was completely released from the WC-Co NPs within a few hours of exposure, although it remained adsorbed/bonded to the particle surface and enabled the adsorption of negatively charged DHBA molecules, in contrast with the WC NPs (no adsorption of DHBA). The DHBA molecules were found to rapidly adsorb on the Co and Cu NPs. The sedimentation of the WC and WC-Co NPs was not influenced by the presence of the 2,3- or 3,4-DHBA molecules. A slight influence (slower sedimentation) was observed for the Co NPs, and a strong influence (slower sedimentation) was observed for the Cu NPs in SW with 2,3-DHBA compared with SW alone. The extent of metal release increased in the order: WC < Cu < Co < WC-Co NPs. All NPs released more than 1 wt-% of their metal total mass. The release from the Cu NPs was most influenced by the presence of DHBA molecules.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Keyword

Cobalt
Copper
Metal release
Nanoparticles
Tungsten
Metal nanoparticles
Metals
Molecules
Sedimentation
Tungsten alloys
Tungsten carbide
3
4-Dihydroxybenzoic acids
Micron-sized particles
Nanoparticle (NPs)
Negatively charged
Physicochemical characteristics
Synthetic surfaces
Tungsten carbide cobalt
Surface waters

Publication and Content Type

ref (subject category)
art (subject category)

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