Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Patterns of deposited colloidal hydrochar formed on glass substrates during the evaporation of water
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).ORCID iD: 0000-0002-8143-8279
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).ORCID iD: 0000-0002-7284-2974
(English)Manuscript (preprint) (Other academic)
Abstract [en]

Patterns of assembled colloidal particles can form on substrates during solvent evaporation and here such  patterns were studied for carbon-rich colloids. Carbon-rich colloids are of fundamental and technological importance, and we prepared monodispersed colloidal hydrochar dispersions by hydrothermal carbonization of glucose. The dispersions were purified by dialysis, and under certain circumstances line patterns formed on the substrates on the evaporation of water and under other circumstances tile-like patterns formed instead. The formation of lines was studied as a function of the addition of sodium dodecylsulfate (SDS), the pH of the dispersion, the geometry of the glass container, and the colloidal particle concentration. The lines consisted of dense assemblies of hydrochar particles. Typically, the lines formed in parallel to the drying front; but on up-concentration, they also formed orthogonally as an effect of likely fingering instabilities. The line width increased with the successive evaporation of water. The horizontal cracks in the tile-like patterns that formed for example without the addition of SDS also formed in parallel to the drying from, and the thickness of the “tiles” increased on successive evaporation of water. The sharper lines that formed on the addition of SDS was tentatively ascribed to the effect of solubilization or moderated interactions. At higher concentrations we obsereved a continuous layer of colloidal particles at the interface also between the lines. The mechanism for the line pattern fromation was derived from the literature on other colloids and for the formation of the tile-like patterns a mechanism was proposed. With this study, we extended the literature on line formation on substrates to a new and important colloidal system – the colloidal hydrochars. The study could also have technological implications to in-situ line printing within microfluidic devices.

Keywords [en]
colloids, hydrothermal carbonization, glucose, monodisperse, repeated line pattern
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:su:diva-198279OAI: oai:DiVA.org:su-198279DiVA, id: diva2:1608518
Funder
EU, Horizon 2020, 721991Available from: 2021-11-03 Created: 2021-11-03 Last updated: 2022-02-25
In thesis
1. Assemblies of Colloidal Hydrochar Nanoparticles and their Derived Activated Carbons for CO2 Sorption
Open this publication in new window or tab >>Assemblies of Colloidal Hydrochar Nanoparticles and their Derived Activated Carbons for CO2 Sorption
2021 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Carbon-rich colloids are of great fundamental and technological interest and in this thesis, I tested a range of hypotheses and studied aspects of small hydrochar-based colloids and their colloidal and material chemistry. Crude hydrochar dispersions were synthesized by hydrothermal carbonization of glucose and purified by dialysis. After the purification, stable and monodisperse dispersions of colloidal hydrochar particles in water were obtained. Evaporation of water from the colloidal hydrochar dispersion led to that the hydrochar particles deposited into repeated strip patterns on glass substrates, or underwent directed assembly into macroscopic rods or yarn-shaped objects at the glass-water-air interface.

In one study, we studied the strip patterns that comprised dense assemblies of hydrochar particles formed through directed assembly on the substrates during evaporation of water as a function of the sodium dodecylsulfate (SDS) addition, pH of the dispersion, geometry of the substrates, and concentration of the colloidal particle. The mechanisms were presented. In the published paper included in the thesis, the formation of the macroscopically large and assembled rods was studied during evaporation of water from the colloidal hydrochar dispersions. This assembly was studied along with the electrostatic stability of the dispersions at various pH and ion strengths and the redispersability of the assembled rods into the constituting colloidal particles. For matters of applications of the rod assemblies, pyrolysis and templating silicon carbide -tricopper silicide ((SiC-Cu3Si) by reactive infiltration with a copper silicon alloy by reaction infiltration were introduced.

In two manuscripts, aspects of the dispersions of hydrochar particles were studied with means of KHCO3 activation into activated carbons (ACs). In one study, hydrochar particles were activated, and then the ACs were dispersed in a solvent after physical grinding. The morphology, porosity, and CO2 sorption properties, etc. of the activated carbons prepared by chemical activation were studied for freeze-dried hydrochar particles and the long bent yarn assemblies pretreated under different conditions. ACs of electrospun nanofibers of polyvinylpyrrolidone (PVP) and colloidal hydrochar were oxidized and chemically activated with KHCO3 or K2CO3 and studied for the adsorption of CO2.

Place, publisher, year, edition, pages
Stockholm: Department of Materials and Environmental Chemistry, Stockholm University, 2021. p. 58
Keywords
colloids, hydrothermal carbonization, glucose, directed assembly, reactive infiltration, templating, silicon carbide, tricopper silicide, redispersion, nanoparticles, chemical activation, activated carbons, CO2 sorption
National Category
Chemical Sciences
Research subject
Materials Chemistry
Identifiers
urn:nbn:se:su:diva-198341 (URN)978-91-7911-692-7 (ISBN)978-91-7911-693-4 (ISBN)
Public defence
2021-12-20, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16 B and online via Zoom, public link is available at the department website, Stockholm, 13:00 (English)
Opponent
Supervisors
Available from: 2021-11-25 Created: 2021-11-04 Last updated: 2022-02-25Bibliographically approved

Open Access in DiVA

No full text in DiVA

Authority records

Wang, XiaHedin, Niklas

Search in DiVA

By author/editor
Wang, XiaHedin, Niklas
By organisation
Department of Materials and Environmental Chemistry (MMK)
Materials Chemistry

Search outside of DiVA

GoogleGoogle Scholar

urn-nbn

Altmetric score

urn-nbn
Total: 66 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf