Etelä-Suomen ensiharvennusmänniköt kuitu- ja energialähteenä

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Ultrastructural evaluation of compression wood-like properties of common juniper (Juniperus communis L.)

Peer reviewe

Optimising and scaling up hot water extraction of tannins from Norway spruce and Scots pine bark

Tannins from Norway spruce (Picea abies [L.] Karst.) and Scots pine (Pinus sylvestris L.) bark were extracted with water at different temperatures (60–140 °C) in an ASE-350 system in order to optimize yield. In addition, the effect of chemicals such as urea, sodium bisulfite (NaHSO3), sodium carbonate (Na2CO3), and sodium benzoate on the yield was also investigated. Bark from debarking processes at both a sawmill and a pulp mill were included. The highest overall yield expressed as total dissolved solids (TDS) was obtained with hot water extraction of spruce bark at 140 °C. The TDS was 117 mg/g and it contained 47 mg/g tannins. With an increase in extraction temperature over 100 °C, the proportion of tannins decreased, whereas the proportion of carbohydrates increased. The addition of sodium carbonate improved yield within a 60–90 °C temperature range compared with pure water. Other chemicals did not improve the yield. Pine bark showed similar extraction yields to spruce bark but the proportion of tannins was lower in spruce than in pine. Pure water at 110 °C was chosen to be used for piloting in larger scale 300-liter extraction vessel. Based on the results, a machine-learning approach was applied using seemingly unrelated regression models (SUR). The models were able to predict the extracted tannin yields of spruce and pine bark when extractions were scaled up to 2 liters and then to 300 liters

Stability and Photoisomerization of Stilbenes Isolated from the Bark of Norway Spruce Roots

Stilbenes or stilbenoids, major polyphenolic compounds of the bark of Norway spruce (Picea abies L. Karst), have potential future applications as drugs, preservatives and other functional ingredients due to their antioxidative, antibacterial and antifungal properties. Stilbenes are photosensitive and UV and fluorescent light induce trans to cis isomerisation via intramolecular cyclization. So far, the characterizations of possible new compounds derived from trans-stilbenes under UV light exposure have been mainly tentative based only on UV or MS spectra without utilizing more detailed structural spectroscopy techniques such as NMR. The objective of this work was to study the stability of biologically interesting and readily available stilbenes such as astringin and isorhapontin and their aglucones piceatannol and isorhapontigenin, which have not been studied previously. The effects of fluorescent and UV light and storage on the stability of trans stilbenes were assessed and the identification and characterisation of new compounds formed during our experiments were carried out by chromatographic (HPLC, GC) and spectroscopic techniques (UV, MS, NMR). The stilbenes undergo a trans to cis isomerisation under extended UV irradiation by intramolecular cyclisation (by the formation of a new C-C bond and the loss of two hydrogens) to phenanthrene structures. The characterised compounds are novel and not described previously

Stability and Photoisomerization of Stilbenes Isolated from the Bark of Norway Spruce Roots

Stilbenes or stilbenoids, major polyphenolic compounds of the bark of Norway spruce (Picea abies L. Karst), have potential future applications as drugs, preservatives and other functional ingredients due to their antioxidative, antibacterial and antifungal properties. Stilbenes are photosensitive and UV and fluorescent light induce trans to cis isomerisation via intramolecular cyclization. So far, the characterizations of possible new compounds derived from trans-stilbenes under UV light exposure have been mainly tentative based only on UV or MS spectra without utilizing more detailed structural spectroscopy techniques such as NMR. The objective of this work was to study the stability of biologically interesting and readily available stilbenes such as astringin and isorhapontin and their aglucones piceatannol and isorhapontigenin, which have not been studied previously. The effects of fluorescent and UV light and storage on the stability of trans stilbenes were assessed and the identification and characterisation of new compounds formed during our experiments were carried out by chromatographic (HPLC, GC) and spectroscopic techniques (UV, MS, NMR). The stilbenes undergo a trans to cis isomerisation under extended UV irradiation by intramolecular cyclisation (by the formation of a new C-C bond and the loss of two hydrogens) to phenanthrene structures. The characterised compounds are novel and not described previously

Determining the composition of lignins in different tissues of Silber Birch

Peer reviewe

The Hydrophobicity of Lignocellulosic Fiber Network Can Be Enhanced with Suberin Fatty Acids

Suberin fatty acids were extracted from outer bark of Silver birch (Betula pendula Roth.) using an isopropanolic sodium hydroxide solution. Laboratory sheets composed of lignocellulosic fiber networks were prepared from unbleached and unrefined softwood kraft pulp and further impregnated with suberin fatty acid monomers and cured with maleic anhydride in ethanol solution. The treatment resulted in hydrophobic surfaces, in which the contact angles remained over 120 degrees during the entire measurement. The fiber network also retained its water vapor permeability and enhanced fiber–fiber bonding resulted in improved tensile strength of the sheets. Scanning electron microscopy (SEM) images revealed that the curing agent, together with suberin fatty acids, was evenly distributed on the fiber surfaces and smoothing occurred over the wrinkled microfibrillar structure. High concentrations of the curing agent resulted in globular structures containing betulinol derivates as revealed with time-of-flight secondary ion mass spectrometry (ToF-SIMS). Also, the larger amount of suberin fatty acid monomers slightly impaired the optical properties of sheets