Iskanje po katalogu digitalne knjižnice

Opis: In this doctorial dissertation subcritical water processes of lignocellulosic biomass to obtain value-added compounds are studied. The doctorial dissertation is divided into four main parts. In the first and second part of dissertation, model compounds (standards of cellulose and sugars and chestnut tannins) were primarly used in order to better understand processes of real biomass material. The degradation of cellulose and different sugars was performed in batch reactor with subcritical water. The different reaction temperatures and times were used. The main phases, such as water-soluble fraction, acetone-soluble fraction and solid residue were separated and analysed. The analysis of water-soluble phase was done by HPLC equipped with UV and RI detector, while acetone-soluble phase of cellulose was analysed by GC-MS. Total sugar content was determined by the phenol-sulphuric acid colorimetric method. The properties of char, obtained using cellulose as a treated material, such as: specific surface area, pore volume and pore diameter were determined by gas adsorption method. A water-soluble phase mainly consists of sugar monomers and monomer degradation products such as 5-hydroxymethylfurfural (5-HMF), furfural, erythrose, sorbitol, 1,6-anhydroglucose, glycolaldehyde, glycerlaldehyde, 1,3-dihydroxyacetone, pyruvaldehyde, formic, levulinic, lactic, oxalic and succinic acids, while acetone-soluble phase, referred to also as bio-oil, consists of furans, phenols, carboxylic acids, aldehydes, ketones and high molecular compounds. The reaction mechanism of cellulose and sugars in subcritical water has been proposed based on the obtained results. Furthermore, the results from cellulose and sugar hydrothermal degradation were utilized in further work to determine which industrially interesting products could be obtained by hydrothermal processing of paper waste in subcritical water. The optimum conditions ( temperature and reaction time), which gave us the highest yield of base chemicals (furfural, 5-HMF, levulinic acid) were determined. Sweet chestnut (Castanea Sativa) bark contains high level of tannins and various phenolic compounds which can be utilized in pharmaceutical, cosmetic, nutritional and medical purposes. The sweet chestnut tannins extract and sweet chestnut bark were used as materials highly rich in bioactive compounds for subcritical water processes which are presented in the second part of doctorial dissertation, respectively. The spectrophotometric methods were used to determine total tannins, phenols and carbohydrates content and antioxidant activity. The identified compounds were ellagic and gallic acid, ellagitannins (vescalagin, castalagin, 1-o-galloyl castalagin, vescalin and castalin), sugars (maltose, glucose, fructose and arabinose) and sugar derivatives (5-HMF, furfural and levulinic acid). The results obtained from hydrothermal hydrolysis were compared to results from acid hydrolysis. Finally, the optimization of reaction parameters of subcritical water processes has been done aiming to obtain the product highly rich in ellagic acid. Subcritical water extraction of horse chestnut (Aesculus hippocastanum) parts such as seeds, seed shell, bark and leaves was described in the third chapter of dissertation. The detected compounds in extracts, such as escins, esculin, fraxin, phenolic compounds (chlorogenic, neochlorogenic and gallic acids) and furfurals (5-hydroxymethyfurfural, furfural, and methylfufrual) are quantified using HPLC. The last part of dissertation proposes extraction of cocoa shell using green technologies (supercritical CO2 and subcritical water extraction) and also conventional methods (Soxhlet extraction with hexane and extraction with 50 % acetone) to obtain bioactive compounds in order to compare the results. The detected compouns were methylxanthines, phenolic compounds, sugars, fatty acids.
Ključne besede: Subcritical water, biomass, biowaste, extraction, hydrothermal degradation, hydrolysis, bioactive compounds.
Objavljeno v DKUM: 16.10.2020; Ogledov: 1094; Prenosov: 134
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Opis: Hydrogen production from aqueous phase reforming (APR) of organic acids in aqueous phase and from residue of a biomass decomposition process over 3 wt% Pt/ZrO2 has been studied in the absence and presence of barium ions. The results have been compared with Pt/TiO2, Pt/C and Ni/C catalysts. Having identified barium hydroxide as a promising reagent in combination with Pt/ZrO2 catalyst for the hydrogen production out of organic acids, the method for the lactic acid conversion was extended. Lactic acid (LA) was analysed as a major compound in an aqueous solution after a biomass digestion process with Ba(OH)2. Gaseous and aqueous products after APR reaction of LA mixture with barium hydroxide were identified by different analytical techniques. Gaseous products consisted mainly of permanent gases such as hydrogen, carbon dioxide and methane. The results showed that mixture of LA in combination with both barium hydroxide and Pt/ZrO2 catalyst had the highest hydrogen production rate and the highest selectivity to hydrogen, whereas low gaseous product amount were observed from mixture of LA and only barium hydroxide or Pt/ZrO2 catalyst. Methane and higher amount of carbon dioxide were detected in gas phase products particular in the presence of Pt/ZrO2 catalyst in the mixture. Aqueous products consisted mainly of pyruvic acid, acetic acid and salts, such as acetate and propionate. The complete conversion of LA after APR was reached in mixture of LA and Ba(OH)2∙8H2O over Pt/ZrO2 catalyst. Mixture of LA and Ba(OH)2∙8H2O or Pt/ZrO2 catalyst gave lower conversion of LA. Amount of gaseous products, selectivity to hydrogen and LA conversion were affected by higher reactant mixture concentration. In comparison to low concentrated mixtures, high concentrated mixtures contained larger amounts of barium but the same amount of Pt/ZrO2 catalyst. BET analyses showed much smaller pore volume of spent Pt/ZrO2 catalyst, which was used in APR reaction of high concentrated (1.5 mol/L) mixture. Therefore, lower gas product amounts, lower selectivity to hydrogen and only 63 % conversion of LA were effects of deactivated Pt/ZrO2 catalyst. The results showed that hydrogen generation from APR of LA and conversion of LA in aqueous phase are hardly influenced by the Pt/ZrO2 catalyst presence, which in combination with barium ions, promotes the catalytic APR reaction.
Ključne besede: biomass, hydrogen production, aqueous phase reforming, lactic acid
Objavljeno v DKUM: 20.02.2015; Ogledov: 1744; Prenosov: 161
Celotno besedilo (2,85 MB)

Opis: Bryophytes are the primary form of carbon storage in many ecosystems. There is growing consensus within the scientific community that increases in atmospheric carbon dioxide (CO2) enhancing the earth's natural greenhouse effect. Because of the potential effects of these gases on the global enery budget and future elimate, there is an urgent need to quantify terrestrial sources and sinks of carbon. There is more carbon stored in some bryophytes than in any other genus of vascular or non-vascular plants (Clymo & Hayward, 1982). Predicting how the vast stores of carbon in moss-dominated ecosystems will be affected by anthropogenic disturbance is critical for models of global climate change (Post et al., 1982). Bryophytes are a prominent feature of many forest and grassland types, where they can make an important contribution to carbon balance (Delucia, et al., 2003). Tropical montane rain forest, because of their complexity and variety of microhabitats, usually harbors a rich diversity of bryophytes. Even though they are often small and inconspicuous, especially in the lowland forest, they may play a significant role in the forest ecosystem (Frahm, 1994). Similarly, bryophytes in the temperate forest and grasslands are thought to be an important carbon sink (O'Neill, 2000). The objective of this research was to estimate components of the bryophyte biomass and approximate amount of carbon stored in it.
Ključne besede: vegetation, habitats, geoelements, carbon, carbon storage, bryophyte, bryophyte biomass
Objavljeno v DKUM: 07.06.2012; Ogledov: 1666; Prenosov: 130
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