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            "title": "Concomitant extraction of bio-oil and value added polysaccharides from Chlorella sorokiniana using a unique sequential hydrothermal extraction technology",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "Moumita",
                    "lastName": "Chakraborty"
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                {
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                    "firstName": "Chao",
                    "lastName": "Miao"
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                {
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                    "firstName": "Armando",
                    "lastName": "McDonald"
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                    "firstName": "Shulin",
                    "lastName": "Chen"
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            ],
            "abstractNote": "To make algal bio-fuel economically viable, extraction of value added co-products along with oil, appears absolutely necessary. The major barrier in algal co-product development is the lack of an efficient separation technology. To address this issue a unique two-step sequential hydrothermal liquefaction (SEQHTL) technology for the simultaneous production of value-added polysaccharides and bio-oil from algal-biomass was developed. The first step involves the subcritical water extraction of valuable algal (Chlorella sorokiniana) polysaccharides at 160 °C. The polysaccharide rich water extract was removed and precipitated with ethanol. In the next step, the extracted biomass was liquefied to bio-oil at 300 °C. The yield of bio-oil by SEQHTL was 24% of the dry weight. In addition, this method also extracted 26% of the polysaccharides present whereas; direct hydrothermal liquefaction (DIRHTL) only generated 28% bio oil. In the SEQHTL method bio-char formation was remarkably low, and as such, SEQHTL produce 63% less bio-char than DIRHTL. The yield of bio-char production is negatively correlated to polysaccharide content (p &gt; 0.98) suggesting majority of carbohydrates present in algal biomass were converted into bio-char. This conversion did not significantly influence the bio-oil production. Comparative GC-FID, GC–MS, NMR, FT-IR analysis and ESI-MS of the bio-oil extracted by SEQHTL with DIRHTL showed no significant differences. Elemental analysis of the SEQHTL bio-oil demonstrated that it contained 70% carbon, 0.8% nitrogen, and 11% oxygen. This method demonstrates an important proof-of-concept step towards the concomitant production of value added co-products, along with bio-oil, from algal biomass.",
            "publicationTitle": "Fuel",
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            "date": "May 2012",
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            "pages": "63-70",
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            "creatorSummary": "Feng et al.",
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            "itemType": "journalArticle",
            "title": "Hydrothermal liquefaction of barks into bio-crude – Effects of species and ash content/composition",
            "creators": [
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                    "creatorType": "author",
                    "firstName": "Shanghuan",
                    "lastName": "Feng"
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                    "firstName": "Matthew",
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                {
                    "creatorType": "author",
                    "firstName": "Chunbao Charles",
                    "lastName": "Xu"
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            ],
            "abstractNote": "Abstract\nLiquefaction of barks of white pine, white spruce and white birch was performed in ethanol–water (50:50, v/v) co-solvents under the initial N2 pressure of 2.0 MPa at 300 °C for 15 min. It was found that the liquefaction efficiency, in terms of bark conversion and bio-crude yield, varied significantly with bark species and ash content/composition. As far as the bark conversion was concerned, the order follows: white spruce bark (92%) &gt; white birch bark (89%) &gt; white pine bark (68%), which is also in good agreement with the ash content of the barks: white spruce bark (3.07%) &gt; white birch bark (2.68%) &gt; white pine bark (1.07%). Bio-crude yield reduced in the following order: white birch bark (67%) &gt; white spruce bark (58%) ≫ white pine bark (36%). Effects of ash content on bark liquefaction were investigated by comparing the liquefaction efficiencies between crude bark and de-ashed bark. Deashing pre-treatment of barks in 0.5 M nitric acid efficiently decreased ash content in barks of white pine, white spruce and white birch form 1.07%, 3.07%, 2.68% to 0.67%, 0.33% and 0.32%, respectively. The de-ashing of bark decreased both bark conversion rate and bio-crude yield for all barks, suggesting that the ash of the bark play catalytic roles in the bark liquefaction, which was confirmed by the addition of K2CO3 and Ca(OH)2 into de-ashed barks. The bark-derived bio-crude oils are aromatic/phenolic in nature with HHVs of 25–39 MJ/kg. The obtained bio-crude oils also have relatively lower molecular weights (Mn = 320–600 g/mol, Mw = 800–1700 g/mol, PDI = 2.2–2.9), which makes the bio-crude oils promising in the applications for either bio-fuel or as a phenol substitute in bio-phenolic resins.",
            "publicationTitle": "Fuel",
            "publisher": "",
            "place": "",
            "date": "January 15, 2014",
            "volume": "116",
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            "pages": "214-220",
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            "title": "Low-temperature catalytic hydrothermal treatment of wood biomass: analysis of liquid products",
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                    "firstName": "Selhan",
                    "lastName": "Karagöz"
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                    "firstName": "Tamiya",
                    "lastName": "Kishimoto"
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            "abstractNote": "Catalytic hydrothermal treatment of wood biomass was performed at 280 °C for 15 min in the presence of alkaline solutions (NaOH, Na2CO3, KOH and K2CO3). Oil products were extracted from both liquid and solid portion by different solvents and analyzed individually. The effect of base solutions on the yield of oil products and composition of oils obtained at different stages were discussed in detail. Based on the conversion and yield of liquid products, the catalytic activity can be ranked as follows: K2CO3 &gt; KOH &gt; Na2CO3 &gt; NaOH. In thermal run, the yield of solid residue was about 42% whereas it was 4.0% in the presence of K2CO3. Catalytic hydrothermal treatment of biomass produced mainly phenolic compounds. In thermal run, furan derivatives were observed whereas these compounds could not be observed in catalytic runs. The volatility distribution of hydrocarbons (ether extract) was characterized by using C-NP gram and it showed that the majority of hydrocarbons for all runs including thermal were distributed boiling point range of n-C11. The products from hydrothermal treatment of wood biomass were analyzed using GC–MS, 1H NMR, 13C NMR, TOC and ion chromatograph.",
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            "title": "Comparative studies of oil compositions produced from sawdust, rice husk, lignin and cellulose by hydrothermal treatment",
            "creators": [
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                    "creatorType": "author",
                    "firstName": "Selhan",
                    "lastName": "Karagöz"
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                    "firstName": "Yusaku",
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            ],
            "abstractNote": "The objective of this study is to investigate the distribution of products, i.e. liquid, gas and solid from wood (sawdust) and non-wood biomass (rice husk), and major biomass components, i.e. lignin, cellulose produced by hydrothermal treatment (280 °C for 15 min) and analysis of liquid hydrocarbons (oils) for the differences in the hydrocarbon composition with respect to feed material. Cellulose showed the highest conversion among the four samples investigated in the present study. Sawdust and rice husk has almost similar conversions. Liquid products were recovered with various solvents (ether, acetone, and ethyl acetate) and analyzed by GC–MS. The oil (ether extract) from the hydrothermal treatment of cellulose consisted of furan derivatives whereas lignin-derived oil contained phenolic compounds. The compositions of oils (ether extract) from sawdust and rice husk contained both phenolic compounds and furans, however phenolic compounds were dominant. Rice husk derived oil consists of more benzenediols than sawdust derived oil. The volatility distribution of oxygenated hydrocarbons were carried out by C-NP gram and it showed that the majority of oxygenated hydrocarbons from sawdust, rice husk and lignin were distributed at n-C11, whereas they were distributed at n-C8 and n-C10 in cellulose-derived oil. The gaseous products were carbon dioxide, carbon monoxide, methane in sawdust, rice husk, lignin and cellulose. In addition to this, ethylene, ethane and propane were observed for sawdust, rice husk and lignin. The major gas product was carbon dioxide for all samples.",
            "publicationTitle": "Fuel",
            "publisher": "",
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            "date": "May 2005",
            "volume": "84",
            "issue": "7–8",
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            "pages": "875-884",
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            "creatorSummary": "Demirbaş",
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            "title": "Thermochemical Conversion of Biomass to Liquid Products in the Aqueous Medium",
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                    "firstName": "Ayhan",
                    "lastName": "Demirbaş"
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            "abstractNote": "We would have to get this one through interlibrary loan.  The article was referenced in another article and the abstract looks promising.\n\nAqueous liquefaction of biomass samples was carried out in an autoclave in the reaction temperature range of 550–650 K. In this study, the maximum liquid yield (49%) was obtained from the spruce wood powder at 650 K. It is clear that the yield of liquid products increase with increasing liquefaction temperature for each biomass sample. In general, composition of liquefaction products depends on structural composition of the sample. The yield of water soluble fraction increases with increasing lignin content of the biomass sample, and the highest water soluble fraction (WSF) yield was obtained for hazelnut shell at liquefaction temperature around 650 K, which was about 21%. The yield of heavy oil generally decreases with increasing lignin content of the biomass sample, and the highest heavy oil yield was obtained for beech wood at liquefaction temperature around 650 K, which was about 28%. The yield of acetone insoluble fraction (residue) decreases with increasing liquefaction temperature for all of runs.",
            "publicationTitle": "Energy Sources",
            "publisher": "",
            "place": "",
            "date": "10/2005",
            "volume": "27",
            "issue": "13",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "1235-1243",
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            "DOI": "10.1080/009083190519357",
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            "creatorSummary": "Toor et al.",
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            "title": "Hydrothermal liquefaction of biomass: A review of subcritical water technologies",
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                    "firstName": "Saqib Sohail",
                    "lastName": "Toor"
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                    "creatorType": "author",
                    "firstName": "Andreas",
                    "lastName": "Rudolf"
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            "abstractNote": "This article reviews the hydrothermal liquefaction of biomass with the aim of describing the current status of the technology. Hydrothermal liquefaction is a medium-temperature, high-pressure thermochemical process, which produces a liquid product, often called bio-oil or bi-crude. During the hydrothermal liquefaction process, the macromolecules of the biomass are first hydrolyzed and/or degraded into smaller molecules. Many of the produced molecules are unstable and reactive and can recombine into larger ones. During this process, a substantial part of the oxygen in the biomass is removed by dehydration or decarboxylation. The chemical properties of bio-oil are highly dependent of the biomass substrate composition. Biomass constitutes of various components such as protein; carbohydrates, lignin and fat, and each of them produce distinct spectra of compounds during hydrothermal liquefaction. In spite of the potential for hydrothermal production of renewable fuels, only a few hydrothermal technologies have so far gone beyond lab- or bench-scale.",
            "publicationTitle": "Energy",
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            "date": "May 2011",
            "volume": "36",
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            "DOI": "10.1016/j.energy.2011.03.013",
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            "shortTitle": "Hydrothermal liquefaction of biomass",
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