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Determining the shape of plant cellulose microfibrils is critical for understanding plant cell wall molecular architecture and conversion of cellulose into biofuels. Only recently has it been determined that these cellulose microfibrils are composed of 18 cellulose chains rather than 36 polymers arranged in a diamond-shaped pattern. This study uses density functional theory calculations to model three possible habits for the 18-chain microfibril and compares the calculated energies, structures, C NMR chemical shifts and WAXS diffractograms of each to evaluate which shape is most probable. Each model is capable of reproducing experimentally-observed data to some extent, but based on relative theoretical energies and reasonable reproduction of all variables considered, a microfibril based on 5 layers in a 34443 arrangement is predicted to be the most probable. A habit based on a 234432 arrangement is slightly less favored, and a 6 × 3 arrangement is considered improbable.
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http://dx.doi.org/10.1038/s41598-018-32211-w | DOI Listing |
PLoS One
September 2025
Department of Life and Environmental Sciences, Polytechnic University of Marche, Ancona, Italy.
Microfibers are pollutants of increasing concern, as they accumulate in aquatic environments and pose risks to living organisms. Once released, they undergo degradation processes that reduce their size and enhance their ability to interact with biological systems. Among these processes, photodegradation is a key driver, leading to fiber fragmentation and structural shrinkage.
View Article and Find Full Text PDFACS Omega
August 2025
Department of Chemistry, 316 Physical Science, Oklahoma State University, Stillwater, Oklahoma 74078, United States.
Detection of hydrogen peroxide (HO) vapor remains a significant challenge for conventional sensing technologies, despite its significance in applications such as the detection of improvised explosive devices (IEDs). Herein, we report a novel, highly sensitive colorimetric sensor system capable of detecting HO vapor at concentrations as low as parts-per-billion (ppb). The sensor is based on a cellulose microfibril network, derived from paper towels, which provides a versatile and tunable substrate for the incorporation of Ti-(IV) oxo complexes.
View Article and Find Full Text PDFCarbohydr Polym
November 2025
Department of Biomaterials Science, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 113-8657 Tokyo, Japan. Electronic address:
Phosphorylated (P-) and TEMPO-oxidized (TO-) wood cellulose fibers (pulps), and P- and TO-cellulose nanofibrils (CNFs) were prepared. To extract pure cellulose molecules, all samples were dispersed in water and freeze-dried, and the P-/TO-pulp and P-/TO-CNF samples were stirred in 8 % (w/w) lithium chloride/N,N-dimethylacetamide (LiCl/DMAc). The quantities of the extracted LiCl/DMAc-soluble fractions and molar-masses of the constituents were determined using size-exclusion chromatography.
View Article and Find Full Text PDFCarbohydr Polym
November 2025
Research Institute for Sustainable Humanosphere, Kyoto University, Uji, Kyoto 611-0011, Japan.
Mechanical properties of wood are governed by its hierarchical organization across multiple length scales. This study hypothesizes that hierarchical structural changes in wood during macroscopic flexural deformation can be detected using in-situ small-angle X-ray scattering (SAXS) and wide-angle X-ray diffraction (WAXD) analysis in synchrotron radiation facility. The in-situ SAXS/WAXD experiments were conducted on water-saturated wood of Japanese larch (Larix kaempferi), with the specimen's length aligned along the tangential (T) direction.
View Article and Find Full Text PDFAnal Chem
August 2025
Department of Chemistry, Michigan State University, East Lansing, Michigan 48824, United States.
The plant secondary cell wall, a complex matrix composed of cellulose, hemicellulose, and lignin, is crucial for the mechanical strength and water-proofing properties of plant tissues, and serves as a primary source of biomass for biorenewable energy and biomaterials. Structural analysis of these polymers and their interactions within the secondary cell wall has been heavily relying on C-based solid-state NMR techniques. In this study, we explore the application of H-detected solid-state NMR techniques for rapid, high-resolution structural characterization of polysaccharides and lignin, demonstrated on the stems of hardwood eucalyptus.
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