1. |
- Bardage, Stig, et al.
(författare)
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The effect of natural product treatment of southern yellow pine on fungi causing blue stain and mold
- 2014
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Ingår i: International Biodeterioration & Biodegradation. - : Elsevier BV. - 0964-8305 .- 1879-0208. ; 86:B, s. 54-59
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Tidskriftsartikel (refereegranskat)abstract
- Blue stain and mold growth on wood can be aesthetically unappealing, but mold growth can also potentially trigger health related issues. In this study, a screening of the effect of selected natural products and derivatives of natural products including essential oils, plant based monomers, and shellfish exoskeleton compounds on the inhibition of blue stain fungi and mold fungi in southern yellow pine veneers and cellulose filter paper. The treatment of the substrates, the weight percent gain of the natural products, and the inhibition effect is presented. The natural products have been investigated previously, but most have not been applied to wood or investigated with regards to blue stain or mold growth. The specimens were treated by dipping, wrapping in foil, and then heating at 105°C for 24h in order to encourage reaction or grafting of the natural products to the wood. A selection of seven additives each exhibited significant protection against blue stain colonization in Petri dish tests and these were studied more in-depth. These included tea tree oil, propyl gallate, hydrogenated gum oil, salicylic acid, cinnamon bark oil, butylene oxide, and furfural. The salicylic acid, tea tree oil, and cinnamon bark oil had the least amount of mold growth after four weeks in the mold chamber test, and have been previously reported to have a mechanism of antifungal activity resulting from their ability to disrupt the fungal cell wall. Propyl gallate veneer was the only specimen that had a lower pH and that would be considered unfavorable to mold growth. While furfural, salicylic acid, and cinnamon bark oil treated veneers all had more hydrophobic surfaces when compared to untreated wood.
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2. |
- Boulanger, Nicolas, et al.
(författare)
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Aramid based slot liners for low voltage electric motor applications
- 2024
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Ingår i: 2024 IEEE Electrical Insulation Conference (EIC). - : IEEE. - 9798350360431 - 9798350360448 ; , s. 17-21
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Konferensbidrag (refereegranskat)abstract
- The insulation in the stator of a low voltage electric motor has a double purpose: ensuring the electric insulation around the stator wiring as well as permitting a good evacuation of the generated heat. Improving the heat transfer properties of the slot liner within the stator while maintaining its electrical insulation properties allows for more efficient electric motors. This paper presents different types of composites based on an aramid matrix with boron nitride, zinc oxide and aluminum oxide fillers. The effect of the different filler materials on the thermal conductivity and the electric insulation properties of the slot liner are presented. Perspectives on the needs for a life cycle assessment of the slot liner constituents are evoked.
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3. |
- Boulanger, Nicolas, et al.
(författare)
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Aramid Based Slot Liners for Low Voltage Electric Motor Applications
- 2024
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Ingår i: 2024 IEEE Electrical Insulation Conference, EIC 2024. - : Institute of Electrical and Electronics Engineers (IEEE). - 9798350360431 - 9798350360448 ; , s. 17-21
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Konferensbidrag (refereegranskat)abstract
- The insulation in the stator of a low voltage electric motor has a double purpose: ensuring the electric insulation around the stator wiring as well as permitting a good evacuation of the generated heat. Improving the heat transfer properties of the slot liner within the stator while maintaining its electrical insulation properties allows for more efficient electric motors. This paper presents different types of composites based on an aramid matrix with boron nitride, zinc oxide and aluminum oxide fillers. The effect of the different filler materials on the thermal conductivity and the electric insulation properties of the slot liner are presented. Perspectives on the needs for a life cycle assessment of the slot liner constituents are evoked.
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4. |
- Claudino, Mauro, et al.
(författare)
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Photoinduced thiol-ene cross-linking of globalide/ε-caprolactone copolymers : curing performance and resulting thermoset properties
- 2012
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Ingår i: Journal of Polymer Science Part A. - : Wiley. - 0887-624X .- 1099-0518. ; 50:1, s. 16-24
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Tidskriftsartikel (refereegranskat)abstract
- The increasing demand for bioderived polymers led us to investigate the potential use of the macrolactone globalide in thermoset synthesis via the photoinduced thiolene reaction. A series of six lipase-catalyzed poly(globalide-caprolactone) copolyesters bearing internal main-chain unsaturations ranging from 10 to 50 and 100 mol % were successfully crosslinked in the melt with equal amounts of thiol groups from trimethylolpropane-trimercapto propionate affording fully transparent amorphous elastomeric materials with different thermal and viscoelastic properties. Three major conclusions can be drawn from this study: (i) high thiol-ene conversions (> 80%) were easily attained for all cases, while maintaining the cure behavior, and irrespective of functionality at reasonable reaction rates; (ii) parallel chain-growth homopropagation of the ene monomer is insignificant when compared with the main thiolene coupling route; and (iii) high ene-density copolymers result in much lower extracted sol fractions and high T(g) values as a result of a more dense and homogeneous crosslinked network. The thiol-ene system evaluated in this contribution serve as model example for the sustainable use of naturally occurring 1,2-disubstituted alkenes in making semisynthetic polymeric materials in high conversions with a range of properties.
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6. |
- Eriksson, Magnus, et al.
(författare)
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Enzymatic One-Pot Route to Telechelic Polypentadecalactone Epoxide : Synthesis, UV Curing, and Characterization
- 2009
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 10:11, s. 3108-3113
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Tidskriftsartikel (refereegranskat)abstract
- In an enzymatic one-pot procedure immobilized lipase B from Candida antarctica was used to synthesize semicrystalline diepoxy functional macromonomers based on glycidol, pentadecalactone, and adipic acid. By changing the stoichiometry of the building blocks. macromonomers of controlled molecular weight front 1400 to 2700 g mol(-1) could be afforded. The enzyme-catalyzed reaction went to completion (conversion >= 95%) within 24 h at 60 degrees C. After removal of the enzyme, the produced macromonomers were used for photopolymerization without any purification. The macromonomers readily copolymerized cationically with a cycloaliphatic diepoxide (Cyracure UVR-6110; CA-dE) to high conversion. The cross-linked copolymers formed a durable film with a degree of crystallinity depending on the macromonomer size and amount of CA-dE used, without CA-dE the macromonomers homopolymerized only to a low degree. Combined with CA-dE conversions of 85-90% were determined by FT-Raman spectroscopy. The films became more durable once reinforced with CA-dE, increasing the cross-link density and reducing the crystallinity of the PDL segments in the films.
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7. |
- Eriksson, Magnus G., et al.
(författare)
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One-pot enzymatic polycondensation to telechelic methacrylate-functional oligoesters used for film formation
- 2011
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Ingår i: POLYM CHEM. - Cambridge : ROYAL SOC CHEMISTRY. - 1759-9954 .- 1759-9962. ; 2:3, s. 714-719
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Tidskriftsartikel (refereegranskat)abstract
- Based on largely renewable monomers, an enzymatic one-pot polycondensation route towards functional oligomers with targeted molecular weights and end-groups was developed. This one-pot synthesis was performed by combining Candida antarctica lipase B (CALB), 2-hydroxyethyl methacrylate (HEMA), ethylene glycol, and divinyl adipate under reduced pressure (72 mbar) at 60 degrees C. The polymerization went to completion (>95% conversion for all monomers) within 24 h and the fraction of methacrylate end-groups was >90%. Three targeted dimethacrylate functional oligomers with molecular weights of 920, 1700 and 2500 g mol(-1) (degrees of polymerization 4, 8, and 13 respectively) were synthesized. The oligomer products were characterized by NMR, MALDI-TOF MS and SEC. The dimethacrylate functional oligomers were further UV homopolymerized or combined with a tetrathiol crosslinker to demonstrate the potential to produce novel networks with tunable thermal properties dependent on chain length of the telechelic building blocks. This research is the first to demonstrate methacrylate functionalization and condensation polymerization in a one step process, which expands the growing toolbox for polymer/material chemists towards an increased throughput in available macromonomers used in material design.
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8. |
- Eriksson, Magnus, et al.
(författare)
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One-Pot Enzymatic Route to Tetraallyl Ether Functional Oligoesters : Synthesis, UV Curing, and Characterization
- 2010
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Ingår i: Journal of Polymer Science Part A. - : Wiley. - 0887-624X .- 1099-0518. ; 48:23, s. 5289-5297
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Tidskriftsartikel (refereegranskat)abstract
- An enzymatic one-pot route in bulk was used to synthesize tetraallyl ether (tAE) functional oligomers based on divinyl adipate, 1,4-butanediol and trimethylolpropane diallyl ether. By using lipase B from Candida antarctica as catalyst and varying the stoichiometric ratio of monomers, it was possible to reach targeted molecular weights (from 1300 to 3300 g mol(-1)) of allyl-ether functional polyesters. The enzyme catalyzed reaction reached completion (>98% conversion based on all monomers) within 24 h at 60 degrees C, under reduced pressure (72 mbar) resulting in similar to 90% yield after filtration. The tAE-functional oligoesters were photopolymerized, without any purification other than removal of the enzyme by filtration, with thiol functional monomers (dithiol, tetrathiol) in a 1: 1 ratio thiol-ene reaction. The photo-initiator, 2,2-dimethoxy-2-phenylacetophenone, was used to improve the rate of reaction under UV light. High conversions (96-99% within detection limits) were found for all thiol-ene films as determined by FT-Raman spectroscopy. The tAE-functional oligoesters were characterized by NMR, MALDI, and SEC. The UV-cured homopolymerized films and the thiol-ene films properties were characterized utilizing DSC and DMTA.
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