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- Hansson, Susanne, et al.
(författare)
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ARGET ATRP for Versatile Grafting of Cellulose Using Various Monomers
- 2009
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Ingår i: ACS Applied Materials & Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 1:11, s. 2651-2659
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Tidskriftsartikel (refereegranskat)abstract
- In recent years, cellulose-based materials have attracted significant attention. To broaden the application areas for cellulose, polymers are often grafted to/from the surface to modify its properties. This study applies ARGET (activators regenerated by electron transfer) ATRP (atom transfer radical polymerization) when straightforwardly grafting methyl methacrylate (MMA), styrene (St), and glycidyl methacrylate (GMA) from cellulose in the form of conventional filter paper In the presence of a sacrificial initiator. The free polymer, formed from the free initiator in parallel to the grafting, was characterized by H-1 NMR and SEC, showing that sufficient control is achieved. However, the analyses also indicated that the propagation from the surface cannot be neglected compared to the propagation of the free polymer at higher targeted molecular weights, which is an assumption often made. The grafted filter papers were evaluated with FT-IR, suggesting that the amount of polymer on the surface increased with increasing monomer conversion, which the FE-SEM micrographs of the substrates also demonstrated. Water contact angle (CA) measurements implied that covering layers of PMMA and PS were formed on the cellulose substrate, making the surface hydrophobic, in spite of low DPs. The CA of the PGMA-grafted filter papers revealed that, by utilizing either aprotic or protic solvents when washing the substrates, it was possible to either preserve or hydrolyze the epoxy groups. Independent of the solvent used, all grafted filter papers were essentially colorless after the washing procedure because of the low amount of copper required when performing ARGET ATRP. Nevertheless, surface modification of cellulose via ARGET ATRP truly facilitates the manufacturing since no thorough freeze-thaw degassing procedures are required.
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| 2. |
- Hao, X. J., et al.
(författare)
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Dendrimers as scaffolds for multifunctional reversible addition-fragmentation chain transfer agents : Syntheses and polymerization
- 2004
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Ingår i: Journal of Polymer Science Part A. - : Wiley. - 0887-624X .- 1099-0518. ; 42:23, s. 5877-5890
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Tidskriftsartikel (refereegranskat)abstract
- The synthesis and characterization of novel first- and second-generation true dendritic reversible addition-fragmentation chain transfer (RAFT) agents carrying 6 or 12 pendant 3-benzylsulfanylthiocarbonylsulfanylpropionic acid RAFT end groups with Z-group architecture based on 1,1,1-hydroxyphenyl ethane and trimethylolpropane cores are described in detail. The multifunctional dendritic RAFT agents have been used to prepare star polymers of poly(butyl acrylate) (PBA) and polystyrene (PS) of narrow polydispersities (1.4 < polydispersity index < 1.1 for PBA and 1.5 < polydispersity index < 1.3 for PS) via bulk free-radical polymerization at 60 degreesC. The novel dendrimer-based multifunctional RAFT agents effect an efficient living polymerization process, as evidenced by the linear evolution of the number-average molecular weight (M.) with the monomer-polymer conversion, yielding star polymers with molecular weights of up to M-n = 160,000 g mol(-1) for PBA (based on a linear PBA calibration) and up to M. = 70,000 g mol(-1) for PS (based on a linear PS calibration). A structural change in the chemical nature of the dendritic core (i.e., 1,1,1-hydroxyphenyl ethane vs trimethylolpropane) has no influence on the observed molecular weight distributions. The star-shaped structure of the generated polymers has been confirmed through the cleavage of the pendant arms off the core of the star-shaped polymeric materials.
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| 3. |
- Hedfors, Cecilia, et al.
(författare)
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Thiol end-functionalization of poly(epsilon-caprolactone), catalyzed by Candida antarctica lipase B
- 2005
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Ingår i: Macromolecules. - : American Chemical Society (ACS). - 0024-9297 .- 1520-5835. ; 38:3, s. 647-649
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Tidskriftsartikel (refereegranskat)abstract
- The use of Candida antarctica Lipase B (CALB) chemoselective catalyst in the Thiol End-Functionalization of Poly(ε-caprolacetone) was discussed. Thiol-functionalization of poly(ε-caprolacetone)(PCL) was made by an initiation reaction catalyzed by CALB in bulk. 2-Mercaptoethanol (1) was used to initiate the enzyme-assisted ring opening polymerization of ε-caprolacetone(2) to give the desired thiol-functionalized polymer. The structure of the terminated PCL was confirmed by 13C nuclear magnetic resonance .
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| 4. |
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| 5. |
- Lindqvist, Josefina, et al.
(författare)
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Intelligent Dual-Responsive Cellulose Surfaces via Surface-Initiated ATRP
- 2008
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 9:8, s. 2139-2145
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Tidskriftsartikel (refereegranskat)abstract
- Novel thermo-responsive cellulose (filter paper) surfaces of N-isopropylacrylamide (NIPAAm) and pH-responsive cellulose surfaces of 4-vinylpyridine (4VP) have been achieved via surface-initiated ATRP. Dual-responsive (pH and temperature) cellulose surfaces were also obtained through the synthesis of block-copolymer brushes of PNIPAAm and P4VP. With changes in pH and temperature, these "intelligent" surfaces showed a reversible response to both individual triggers, as indicated by the changes in wettability from highly hydrophilic to highly hydrophobic observed by water contact angle measurements. Adjusting the composition of the grafted block-copolymer brushes allowed for further tuning of the wettability of these "intelligent" cellulose surfaces.
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| 8. |
- Mulla, Yusuf, et al.
(författare)
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Bio-Graphene Sensors for Monitoring Moisture Levels in Wood and Ambient Environment
- 2023
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Ingår i: Global Challenges. - : John Wiley and Sons Inc. - 2056-6646. ; 7:4
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Tidskriftsartikel (refereegranskat)abstract
- Wood is an inherently hygroscopic material which tends to absorb moisture from its surrounding. Moisture in wood is a determining factor for the quality of wood being employed in construction, since it causes weakening, deformation, rotting, and ultimately leading to failure of the structures resulting in costs to the economy, the environment, and to the safety of residents. Therefore, monitoring moisture in wood during the construction phase and after construction is vital for the future of smart and sustainable buildings. Employing bio-based materials for the construction of electronics is one way to mitigate the environmental impact of such electronics. Herein, a bio-graphene sensor for monitoring the moisture inside and around wooden surfaces is fabricated using laser-induced graphitization of a lignin-based ink precursor. The bio-graphene sensors are used to measure humidity in the range of 10% up to 90% at 25 °C. Using laser induced graphitization, conductor resistivity of 18.6 Ω sq−1 is obtained for spruce wood and 57.1 Ω sq−1 for pine wood. The sensitivity of sensors fabricated on spruce and pine wood is 2.6 and 0.74 MΩ per % RH. Surface morphology and degree of graphitization are investigated using scanning electron microscopy, Raman spectroscopy, and thermogravimetric analysis methods. © 2023 The Authors.
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