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The use of polyphenol extracts from radiata pine (Pinus radiata) bark as raw materials for bio-foams was investigated along with the optimal NaOH extraction conditions. The targeted yield of alkaline extracts was 60%, and the targeted pH was 11 to 12. The radiata pine bark was composed of 70% of a 1% NaOH extract, which contained mainly polyphenols, such as proanthocyanidin (PA). As the particle size of the bark decreased, the yield of the 1% NaOH extracts increased from 57 to 87%. A range of NaOH concentrations, liquor ratios, and extraction times were explored to establish an economic polyphenol extraction method. More than 60% of the alkaline extract was extracted, and the pH of the extract was approximately 12 when the optimum extraction conditions were employed, i.e., a liquor to bark ratio of 5:1, a NaOH dosage of 17 to 18% based on the bark weight, and a 1 h extraction time. Following neutralization of the alkaline extract, structural analysis indicated severe structural changes in the PA during the alkaline extraction. Because the alkaline extract was barely soluble in the solvent used for the structural analyses, it is assumed that chemical modification is required to increase the solubility of the alkaline extract for the production of bio-foams.

To date, Korean hinoki cypress (Chamaecyparis obtusa), has been widely used for household and commercial purposes. Although the medicinal efficacy of hinoki cypress essential oil has been observed, that of the essential oil-derived terpenes, which exhibit a mechanism that acts against lung inflammation, remains to be fully elucidated. The present study investigated the anti-inflammatory effect of hinoki cypress leaf extracted essential oil on lipopolysaccharide (LPS)-stimulated WI38 fibroblast cells by inhibiting the nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB) pathway, which exhibited lung tissue protection through the olfactory administration of essential oil in Sprague-Dawley rats. GC/MS analysis derived 24 terpenes from the essential oil. The morphological observations revealed that, upon LPS stimulation of WI38 fibroblast cells, inflammation was induced, whereas the condition of the cells reverted to normal in the essential oil extract pre-treated group. The results of western blot analysis revealed the inhibition of inducible nitric oxide synthase, activation of cyclooxygnase-2, and the degradation of cytosolic p65 and inhibitor of NF-κB-α in the LPS-stimulated group. Additionally, confocal imaging of nuclei revealed the translocation of phosphorylated p65, which was recovered in the cytosol in the phytoncide essential oil pre-treated group. Histopathological observation revealed that the alveolar capacity was enhanced in the essential oil olfactory administered rat group, compared with that in the normal rat group. These findings suggest that terpenes in essential oil from the Chamaecyparis obtusa leaf have therapeutic potential against respiratory inflammation-related disease.

The mountain pine beetle-killed lodgepole pine ( Pinus contorta ) wood treated with iron (III) nitrate solution was used for the preparation of Fe-cored carbon nanomaterials (Fe-CNs) under various carbonization temperatures. The carbonization yield of Fe-treated sample (5% as Fe) was always 1–3% higher (after ash compensation) than that of the non-treated samples heated at the same condition. The lowest carbonization temperature required to produce Fe-CNs was 700 °C. The carbon shell was composed of 30–40 well-aligned layers of graphitic carbon nanostructure. The iron captured by graphitic layers was assumed to be iron carbides and/or α-Fe and γ-Fe. This study indicates that at least 700 °C of carbonization temperature is needed for the production of Fe-CNs and the mountain pine beetle-killed pine wood can be a carbon source for the production of Fe-CNs.

Easter red cedar (Juniperus virginiana) is a valuable source of heartwood extractives that provide decay resistance against termites and wood decay fungi. This study sought to determine the antifungal activity of heartwood extracts obtained using solvents with increasing polarity (hexane, chloroform, ethyl acetate, and methanol) against two wood decay fungi. The heartwood was extracted with methanol, and the methanol extract was sequentially extracted with hexane, chloroform, and ethyl acetate. The yield of the methanol extractives was 5.26 percent based on dry wood and the percentages of the hexane, chloroform, and ethyl acetate soluble fractions from the methanol extract were 46.4, 8.3, and 28.7 percent, respectively. Hexane and chloroform soluble fractions showed a high inhibitory effect on the growth of the wood decay fungi Trametes versicolor and Gloeophyllum trabeum. Gas chromatography–mass spectrometry analysis identified skeletons of sesquiterpenes and sesquiterpene alcohols in both extracts and t...

Lack of data especially pertaining to the chemistry of mangrove wood species makes it difficult to prepare successful plans for their conservation and to use mangroves as a source of wood fiber. In this paper, chemical characterizations of the six main mangrove species of Bangladesh [namely Keora (Sonneratia apetala), Geoa (Excoecaria agallocha), Bine (Avicennia alba), Sundari (Heritiera fomes) Pashur (Xyloccarpous mekongests), and Kakra (Bruguiera gymnorhiza)] were investigated. The chemical results revealed that these species contain high percentages of dichloromethane followed by methanol extractives. Methanol extracts in Pashur, Sundari, and Bine were higher than 10%, which indicates high percentage of tannin material. The total lignin content in these species was higher than 25%, except for Gewa (23.6%) and Pashur (21.3%), which is higher than that of the normal range of hardwood. The pentosan content in these six species was within the range of 19.4–22.8%. The α-cellulose content in Keora and Gewa was acceptable for pulp production, but the others were lower than the normal range of hardwood. Alkaline nitrobenzene oxidation showed that all these species had a very high syringaldehyde to vanillin (2.6–5.0) ratio except Keora (1.6). Surprisingly, rhamnose is the main constituent with xylose of hemicelluloses of these six mangrove species. The ash content in these six mangrove wood species was also higher than that in normal hardwood.

Dioxane and milled wood lignins (MWL) were isolated from tropical hardwood, Nalita (Trema orientalis ) and temperate hardwood, aspen. These lignins were characterized by UV, FTIR, 1 H-NMR and 13 C-NMR spectroscopy, alkaline nitrobenzene oxidation, molecular weight determination, elemental and methoxyl analysis. The structural analysis revealed that Nalita and aspen lignin is syringyl-guaiacyl type. Aspen lignin had higher syringyl unit than Nalita lignin. The β-O-4 type linkages are the main interunit linkages and more abundant in aspen than Nalita. Dioxane lignin showed higher free phenolic hydroxyl group than MWL in both species. The weight average molecular weight of aspen lignin was lower than that of Nalita lignin. Nalita and aspen lignins contained both erythro and threo configuration, but erythro proton gave stronger peak. A UV absorption maximum of aspen lignin was at 274 nm, whereas it was shifted to 280 nm for Nalita lignin. Keywords: Trema orientalis , Aspen, Dioxane lignin, Milled wood lignin, Syringyl-guaiacyl, β-O-4 linkages DOI: 10.3329/bjsir.v44i3.4399 Bangladesh J. Sci. Ind. Res. 44(3) , 271-280, 2009

The chemical composition of natural powder dye manufactured from Pinus radiata bark and dyeability of dyed silk fabrics with were examined. It is made up of the optimum dyeing condition of silk fabric according to the dyeing concentration, dyeing time, and dyeing temperature. Also, we examined the colorfastness and antibiosis of dyed silk fabrics to washing, rubbing, perspiration and light. For the analysis of the chemical composition of , the total contents of phenolic compound, proanthocyanidin(PA) and anti-oxidative activities of the dye were analyzed. As a result, it was found that the main components of the manufactured from Pinus radiata bark is proanthocyanidin, mostly a flavonoid containing a procyanidin structure, and it consists of approximately 63% phenol. As a result of examining the dyeability of silk fabrics with , it showed that the dyeability was best under the conditions of the concentration of dye (wt/v%), dyeing time of 90 minutes, and dyeing temperature at . It was found that the colorfastness of dyed silk fabrics, colorfastness to washing, perspiration for acidic and rubbing were as good as grade 4 or 4-5. However, the colorfastness to light was low at grade 1, the same as the results of other natural dyed fabrics. As a result of the antibiosis measurement for the -dyed silk fabrics, it showed high antibacterial properties to Staphylococcus sureus at 99.6%.

Constituents of tars formed during the aging of bamboo (Phyllostachys pubescens), oak (Quercus serrata), and pine (Pinus densiflora) wood crude vinegars were analyzed by pyrolysis-gas chromatography (Py-GC) and pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS) to investigate their origination. The pyrolysate of tars obtained from the wood and bamboo crude vinegars were almost identical and were primarily composed of phenolic compounds and aromatic hydrocarbons. In addition, during the aging of model wood vinegar that was prepared for comparison with the wood and bamboo vinegars, a marked decrease was observed in the levels of phenolic compounds (phenol; o-, p-, and m-cresol; and syringol). Furthermore, the Py-GC-MS results of the tars produced during the aging of the model wood vinegar revealed that phenolic compounds were primarily responsible for the formation of tar during the aging of wood and bamboo crude vinegars. Pyrroles, which may be derived from the primary pyrolysate of amino acids, nitrogen-containing extracts, or both, were also partially involved in the formation of tar during the aging period.

Pine (Pinus densiflora) bark was chemically modified by grafting with acrylonitrile (AN) through Fenton reaction and conversion of the cyano group to an amidoxime group by reaction with hydroxylamine. Treatments of pine bark with 160 mM H2O2 at 40°C yielded ~70% grafting in 6-h reaction. After alkali hydrolysis of amidoximated pine bark (AOPB), its adsorption capacity (q e) for copper ions was largely increased from 0.5 to 1.8 mmol/g. Adsorption of the hydrolyzed AOPB (HAOPB) followed the pseudo-second-order kinetic model. Among the metal ions tested, the order of adsorption capacity (q e) predicted by the kinetic model at equilibrium time was Hg2+ > UO2 2+ > Cd2+ > Cu2+ > Zn2+ > Ni2+. The adsorption process was pH-dependent, and the adsorption equilibrium was observed in the pH range of 6–7 for all the metal ions. Even though pine bark is a good adsorbent for Hg2+ and UO2 2+ ions, it had a poor affinity for the other ions tested. It was obviously found that HAOPB had very high adsorption abilities for heavy metal and uranyl ions.

The phenolic composition of pine bark from a variety of Pinus species was estimated by measuring Klason lignin, acid-soluble lignin, and a 1% NaOH extract. Polyphenol contents of hot water extracts from pine bark were determined by the Folin-Ciocalteu assay and the vanillin-H2SO4 assay. Among the pine bark varieties investigated, Pinus radiata bark showed the highest polyphenol content and potent antioxidant activity. Pinus rigida bark was also a usable polyphenol-rich source, whereas Pinus densiflora bark had a low yield (5.1%) of hot water extract, although it showed potent antioxidant activity. Correlations between proanthocyanidin content in pine bark and antioxidant activity were observed. The results suggested that proanthocyanidin was the crucial contributor to potent antioxidant activity in pine bark.

Nalita (Trema orientalis) is one of the fastest growing trees in the tropical countries. The structural characteristics of lignin isolated at different ages of Nalita wood (Trema orientalis) by acidolytic dioxane method were examined by UV, FTIR, 1H‐NMR and 13C‐NMR spectroscopy, alkaline nitrobenzene oxidation, molecular weight determination, elemental and methoxyl analysis. The data were compared with aspen lignin. The structural analysis revealed that Nalita wood lignin is syringyl‐guaiacyl type. The methoxyl content in Nalita wood lignin was lower than aspen lignin. The C9 formulas for 30‐months‐old Nalita was C9H9.31O3.13(OCH3)1.27, whereas that of aspen was C9H8.94O3.15(OCH3)1.47. The weight average molecular weight of Nalita wood lignin was decreased from 36,500 to 25,500 with increasing tree age from 12 to 30 months, whereas weight average molecular weight of aspen was 20,000. Both alcoholic and phenolic hydroxyl group in Nalita wood lignin is lower than aspen lignin.

Batch biosorption experiments were carried out for the removal of Congo red from aqueous solution using native and pretreated mycelial pellets/biomass of Trametes versicolor. The effect of process parameters such as contact time, dye concentration, and pH on the extent of Congo red biosorption has been investigated. Higher dye concentrations resulted in lower biosorption. Increases in biomass dosage led to increases in the levels of biosorption. Biosorption kinetics and equilibrium data are essential basic requirements to develop an effective and accurate design model for the removal of the dye. A kinetic study showed that the biosorption of the dye on fungal biomass was a gradual process. Pseudo-first-order, pseudo-second-order, and Bangham's model were used to fit the experimental data. The results of the kinetic studies showed that the second-order kinetic model fitted well for the present experimental data. Equilibrium isotherms were analyzed by Langmuir, Freundlich, Dubnin-Radushkevich, and Temkin isotherms. The biosorption equilibrium data obeyed the Langmuir and Temkin isotherms well. Acidic pH was favorable for the biosorption of the dye. Studies on the pH effect and desorption show that chemisorption seems to play a major role in the biosorption process. Among the native and pretreated biomass studied, autoclaved biomass showed a better biosorption capacity.

The change of crystalline structure of Nalita cellulose with tree age has been studied using X-ray diffraction and FT-IR spectroscopy. The proportion of crystallinity and crystal size were increased with tree age. FT-IR spectroscopy showed that the Nalita cellulose was a monoclinic unit cell structure (Iβ). The proportion of crystallinity and crystal size of the 30-month-old Nalita wood was higher as compared to aspen wood. The degree of polymerization (DP) of Nalita cellulose of different ages has also been studied. The DP of cellulose increased with tree age. The DP of Nalita cellulose was lower than that of aspen cellulose. The percentage of glucose in Nalita wood increased with tree age.

A chloroform fraction prepared from the sarcotesta of Ginkgo biloba showed potent inhibitory activity against vancomycin-resistant Enterococcus (VRE). The active compounds were elucidated to be 2-hydroxy-6-(8-pentadecenyl) salicylic acid (1) and 2-hydroxy-6-(10-heptadecenyl) salicylic acid (2) based on their spectral analysis. Compounds 1 and 2 showed significant antibacterial activities against VRE.

The extraction of anthocyanin from Bokbunja ( Rubus coreanus Miq.) marc generated during traditional wine processing was optimized using response surface methodology (RSM). A face-centered cube design (FCD) consisting of 17 experimental runs, including five replicates at the center point, was used to investigate the effects of the three variables (solid–liquid ratio, time, and temperature) on anthocyanin extraction, and the results showed that the relationship between the three variables and the total anthocyanin content followed a quadratic model ( R 2 = 0.8853). In addition, the RSM analysis predicted that the optimum conditions for extraction consisted of a solid–liquid ratio of 20, a time of 60 min, and a temperature of 60 °C. Verification tests performed under these optimum conditions gave 34.7 ± 1.4 mg/100 g of anthocyanin, which was close to predicted value of 37.2 mg/100 g. Additionally, analysis of water extracts prepared using the predicted optimum conditions revealed that the carbohydrates (sugar and pectin) in Bokbunja marc underwent significant variation toward the formation of by-products (glycerol and uronic acids) during yeast fermentation, and that the amount of anthocyanin produced was reduced 10-fold when compared to the original extraction. Further, the results of HPLC-PDA-MS/MS analysis of the anthocyanins extracted from Bokbunja marc revealed the presence of six anthocyanin components, which were tentatively identified as cyanidin 3- O -sambubioside, cyanidin 3- O -xylosylrutinoside, cyanidin 3- O -rutinoside, pelargonidin 3- O -rutinoside, delphinidin 3- O -rutinoside-?, and delphinidin 3- O -glucuronide.

The antioxidant potential of ethanol extracts from defatted Bokbunja seed wastes generated during wine processing were estimated by radical scavenging abilities (DPPH(*), H(2)O(2), and O(2)(*-)), retardation of lipid oxidation, and iron ion-chelating characteristics. For comparison, ethanol extracts from seeds of fresh ripe Bokbunja fruits were also used. The ethanol extracts from the wine seed waste always showed higher scavenging activities against DPPH(*), H(2)O(2), and O(2)(*-) than those from the fresh seeds. The oxidation of linoleic acid in dimethylsulfoxide at 105 degrees C revealed that the kinetic behavior clearly obeyed pseudo-zero-order regardless of the linoleic acid concentration. The Fe(II)-chelating capacity was determined by the Freundlich isotherm. The results showed high potential and favorability of the two extracts for Fe(II) chelation. The Freundlich chelation capacities (mg(1-1/n)L(1/n)/g) of both ethanol extracts from seeds of fresh Bokbunja and wine processing wastes, tannic acid, and proanthocyanidin from Pinus radiata bark were 100, 224, 260, and 307, respectively. The Fe(III)-chelating properties of the ethanol extracts were considered to be deeply associated with its 3',4',5'-trihydroxyl (galloyl) group as with tannic acid.

The physicochemical characteristics, fatty acid (FA) profile, and triacylglyceride (TAG) composition of seed oils from fresh Bokbunja (Rubus coreanus Miq.) fruits and traditional Bokbunja wine processing waste were determined in this study. Oil contents of the fresh seeds and the seeds from wine processing waste were similar, accounting for about 18% of dry weight. The free fatty acid (FFA) content between the two seed oils was significantly different (0.50% for fresh seed oil and 73.14% for wine seed oil). Iodine, conjugated diene, saponification values, and unsaponifiable matter were very similar in the oil samples, but the specific extinction coefficients at 232 and 270 nm of wine seed oil were higher than those of fresh seed oil. Linoleic (C18:2, 50.45-53.18%, L) and linolenic (C18:3, 29.36-33.25%, Ln) acids were the dominant FAs in the two seed oils, whereas oleic (C18:1, 7.32-8.04%, O), palmitic (C16:0, 1.55-1.65%, P), and stearic (C18:0, 0.65-0.68%, S) acids were the minor FAs. LLL, OLL, LLLn, OOL, LLnLn, and OOO were the abundant TAGs, representing >90% of the oils.