Alar Konist

Prof. Alar Konist

orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 April 2022 in Materials
Verified
Journal Article
Open access
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PJPiia Jõul
Piia Jõul
THTran T. Ho
Tran T. Ho
UKUrve Kallavus
Urve Kallavus
Alar KonistAlar Konist
Alar Konist
KLKristiina Leiman
Kristiina Leiman
Tiit LukkTiit Lukk
Tiit Lukk
The production of novel materials and value-added chemicals from lignin has received considerable attention in recent years. Due to its abundant occurrence in nature, there is a growing interest in utilizing lignin as a feedstock for functional materials production, for example aerogels. Much like in the synthesis of phenol-based resins, the vacant ortho positions of the aromatic rings in lignin can crosslink with formaldehyde and form polymeric gels. After drying the hydrogels with supercritical CO2, highly porous aerogels are obtained. Current study focuses on the preparation and thorough parametrization of organosolv lignins from different types of lignocellulosic biomass (aspen, pine, and barley straw) as well as their utilization for the preparation of lignin-5-methylresorcinol-formaldehyde aerogels. The thorough structural characterization of the obtained aerogels was carried out by gas adsorption, IR spectroscopy, and scanning electron microscopy. The obtained lignin-based monolithic mesoporous aerogels had specific surface areas and total pore volumes in the upward ranges of 450 m2/g and 1.4 cm3/g, respectively.

1 March 2012 in Fuel
Verified
Journal Article
Closed access
TPT. Pihu
T. Pihu
HAH. Arro
H. Arro
APA. Prikk
A. Prikk
RRR. Rootamm
R. Rootamm
Alar KonistAlar Konist
Alar Konist
RMR. Mõtlep
R. Mõtlep

1 June 2015 in Fuel Processing Technology
Verified
Journal Article
Closed access
LLLauri Loo
Lauri Loo
BMBirgit Maaten
Birgit Maaten
Andres SiirdeAndres Siirde
Andres Siirde
TPTõnu Pihu
Tõnu Pihu
Alar KonistAlar Konist
Alar Konist

1 December 2017 in Fuel Processing Technology
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Journal Article
Closed access
NRNenad D. Ristic
Nenad D. Ristic
MDMarko Djokic
Marko Djokic
Alar KonistAlar Konist
Alar Konist
KGKevin M. Van Geem
Kevin M. Van Geem
GMGuy B. Marin
Guy B. Marin

25 October 2021 in Sustainability
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Journal Article
Open access
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ACAlejandro Lyons Ceron
Alejandro Lyons Ceron
Alar KonistAlar Konist
Alar Konist
HLHeidi Lees
Heidi Lees
OJOliver Järvik
Oliver Järvik
Using woody biomass in thermochemical gasification can be a viable alternative for producing renewable energy. The type of biomass and the process parameters influence the producer gas composition and quality. This paper presents research on the composition of the producer gas from the gasification of three woody biomass species: spruce, alder, and pine. The experiments were conducted in a drop-tube reactor at temperatures of 750, 850, and 950 °C, using air as the gasifying agent, with equivalence ratios of 0.38 and 0.19. Gas chromatography with a thermal conductivity detector was used to determine the composition of the producer gas, while the production of total organic compounds was detected using Fourier-transform infrared spectroscopy. All three wood species exhibited very similar producer gas composition. The highest concentration of combustible gases was recorded at 950 °C, with an average of 4.1, 20.5, and 4.6 vol% for H2, CO, and CH4, respectively, and a LHV ranging from 4.3–5.1 MJ/m3. The results were in accordance with other gasification studies of woody species. Higher temperatures enhanced the composition of the producer gas by promoting endothermic and exothermic gasification reactions, increasing gas production while lowering solid and tar yields. The highest concentrations of combustible gases were observed with an equivalence ratio of 0.38. Continuous TOC measurement allowed understanding the evolution of the gasification process and the relation between a higher production of TOC and CO as the gasification temperature raised.

1 March 2019 in Science of The Total Environment
Verified
Journal Article
Open access
KLKristjan Leben
Kristjan Leben
RMRiho Mõtlep
Riho Mõtlep
PPPeeter Paaver
Peeter Paaver
Alar KonistAlar Konist
Alar Konist
TPTõnu Pihu
Tõnu Pihu
KKKalle Kirsimäe
Kalle Kirsimäe
Power generation and other industries using solid fossil fuels like coal, lignite, oil shale and peat are responsible for producing large quantities of solid residues that are often chemically reactive and/or unstable and are disposed in holding ponds and deposition sites. Stability and long-term behaviour of such deposits are typically studied in short-term laboratory experiments that cannot describe nor predict long-term changes taking place in these materials. Here, we study long-term (>40 years) transformations, in highly alkaline conditions, of the Ca-rich ash deposit in Estonia composed of oil shale processing residues from the Eesti power plant. Detailed mineralogical, chemical and micromorphological analyses using X-ray diffraction, X-ray fluorescence, 29Si nuclear magnetic resonance, scanning electron microscopy and other methods were applied in order to identify the composition of the waste with a focus on formation and transformation of semicrystalline phases in the deposit. The results show progressive formation of calcium-silicate-hydrate (C-S-H) type phase at the expense of silicate minerals and amorphous glass phases with increasing depth and age of the sediments, from about 25% in the upper part of the depository to over 60% in the oldest-deepest part. This demonstrates that over time the high alkalinity of the ash is responsible for initiating natural alkali-activation. The formation of C-S-H-type phases increases the mechanical strength of the sediment and ensures long-term stability of waste deposits. These findings may encourage the use of these ashes in binder or other construction material production or as construction aggregates.