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<Gradivo ID="29286" NadgradivoID="1713" NRID="28553970" OceID="0" DomainUrl="https://dirros.openscience.si/" IzpisPolniUrl="https://dirros.openscience.si/IzpisGradiva.php?lang=slv&amp;id=29286" StOgledov="47" StPrenosov="41" StOcen="0" VsotaOcen="0" DatumIzvoza="2026-05-09 16:56:27" OcenaSkupna="0" StPodgradiv="1" StudijskiProgramEvsID="" JeIndeksirano="0" JeVecAvtorjev="0" DovoliZahtevkeZaDostop="0">
  <PID Url="http://hdl.handle.net/20.500.12556/DiRROS-29286">20.500.12556/DiRROS-29286</PID>
  <Naslov>Effect of alkali-activation pre-treatment of sintered aggregates from biomass fly ash on microstructural and mineralogical evolution</Naslov>
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  <Opis>The increasing demand for lightweight construction materials and the depletion of natural aggregates highlight the need for circular solutions based on industrial residues. Co-incineration biomass ash (BA), despite its high availability, carbon content, and variable composition, remains underutilised in high-value applications. This study explores a previously unexamined valorisation route through the production of sintered alkali-activated aggregates using sodium-silicate-assisted pre-treatment. Two BA mixes with different Na2O dosages (7.57 and 5.44 wt% Na2O) were pelletized and thermally treated between 700 and 1200 ◦C. The alkali activation pretreatment simultaneously improved the granulation efficiency, enabled the formation of alkali-activated gel, and supplied Na2O as a flux, significantly influencing the crystalization, melting, and sintering behavior. Comprehensive characterisation using mercury intrusion porosimetry, dilatometry, X-ray diffraction, Fouriertransform infrared spectroscopy, thermogravimetry–differential thermal analysis, and scanning electron microscopy revealed a coherent thermal sequence: from gel deterioration and a macroporosity development below 800 ◦C, to the crystallization of Ca–Mg silicates and the formation of an akermanite-dominated matrix at 800–1000 ◦C, followed by partial melting and sintering in the presence of a liquid phase above 1000 ◦C. A higher alkali content promoted earlier densification and strength development. Aggregates with higher Na2O content (BA1) exhibited an earlier onset and higher intensity of sintering shrinkage, reaching a compressive strength of 4.53 MPa at 1100 ◦C, corresponding to more than a fourfold increase compared to thermally untreated aggregates, whereas the lower-alkali mix (BA2) remained below 0.26 MPa at the same temperature. Open porosity of BA1 aggregates increased to 78.8% after heating to 800 ◦C due to deterioration of the alkali-activated gel, followed by densification accompanied by akermanite-dominated crystallization and pore coalescence, resulting in 73.1% porosity and a bulk density of 1.28 g/cm3 at 1100 ◦C. The results identify BA as a promising precursor for lightweight or dense SAA and demonstrate alkali-activation-assisted thermal treatment to be a technically applicable circular-economy pathway for converting co-incineration BA into value-added construction materials.</Opis>
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  <KljucneBesede>
    <Beseda>alkali-activated materials</Beseda>
    <Beseda>biomass ash</Beseda>
    <Beseda>sintered aggregates</Beseda>
    <Beseda>lightweight aggregates</Beseda>
  </KljucneBesede>
  <TujJezik_KljucneBesede>
    <Beseda>alkalijsko aktivirani materiali</Beseda>
    <Beseda>biomasni pepel</Beseda>
    <Beseda>sintrani agregati</Beseda>
    <Beseda>lahki agregati</Beseda>
  </TujJezik_KljucneBesede>
  <Potrjeno>true</Potrjeno>
  <JeZaklenjeno>false</JeZaklenjeno>
  <JeRecenzirano>true</JeRecenzirano>
  <Zaloznik>Elsevier</Zaloznik>
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  <Jezik ID="1033" ISO639-3="eng">Angleški jezik</Jezik>
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  <AvtorskePravice>© 2026 The Authors</AvtorskePravice>
  <VrstaGradiva ID="" DRIVER="info:eu-repo/semantics/other">Neznano</VrstaGradiva>
  <DatumVstavljanja>2026-05-06 11:24:43</DatumVstavljanja>
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  <DatumSpremembe>2026-05-07 03:51:13</DatumSpremembe>
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  <LetoIzida>2026</LetoIzida>
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  <StStrani>str. 19392-19407</StStrani>
  <StevilcenjeNivo1>part B</StevilcenjeNivo1>
  <StevilcenjeNivo2>issue 12</StevilcenjeNivo2>
  <Kronologija>May 2026</Kronologija>
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  <Patent_DatumVeljavnosti>0000-00-00</Patent_DatumVeljavnosti>
  <VerzijaDokumenta>Zaloznikova</VerzijaDokumenta>
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  <DatumObjaveClanka>2026-03-04</DatumObjaveClanka>
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