scholarly journals Hydrothermal Liquefaction of Food Waste: Effect of Process Parameters on Product Yields and Chemistry

2021 ◽  
Vol 5 ◽  
Author(s):  
Hengameh Bayat ◽  
Mostafa Dehghanizadeh ◽  
Jacqueline M. Jarvis ◽  
Catherine E. Brewer ◽  
Umakanta Jena

Increasing food waste generation (1.6 billion tons per year globally) due to urban and industrial development has prompted researchers to pursue alternative waste management methods. Energy valorization of food waste is a method that can reduce the environmental impacts of landfills and the global reliance on crude oil for liquid fuels. In this study, food waste was converted to bio-crude oil via hydrothermal liquefaction (HTL) in a batch reactor at moderate temperatures (240–295°C), reaction times (0–60 min), and 15 wt.% solids loading. The maximum HTL bio-crude oil yield (27.5 wt.%), and energy recovery (49%) were obtained at 240°C and 30 min, while the highest bio-crude oil energy content (40.2 MJ/kg) was observed at 295°C. The properties of the bio-crude oil were determined using thermogravimetric analysis, fatty acid methyl ester (FAME) analysis by gas chromatography with flame ionization detection, CHNS elemental analysis, and ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectroscopy (FT-ICR MS). FT-ICR MS results indicated that the majority of the detected compounds in the bio-crude oil were oxygen-containing species. The O4 class was the most abundant class of heteroatom-containing compounds in all HTL bio-crude oil samples produced at 240°C; the O2 class was the most abundant class obtained at 265 and 295°C. The total FAME content of the bio-crude oil was 15–37 wt.%, of which the most abundant were palmitic acid (C16:0), palmitoleic acid (C16:1), stearic acid (C18:0), and polyunsaturated fatty acids (C18:3N:3, C18:3N:6).

Energies ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 2766 ◽  
Author(s):  
Jandyson Santos ◽  
Alberto Wisniewski Jr. ◽  
Marcos Eberlin ◽  
Wolfgang Schrader

Different ionization techniques based on different principles have been applied for the direct mass spectrometric (MS) analysis of crude oils providing composition profiles. Such profiles have been used to infer a number of crude oil properties. We have tested the ability of two major atmospheric pressure ionization techniques, electrospray ionization (ESI(±)) and atmospheric pressure photoionization (APPI(+)), in conjunction with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). The ultrahigh resolution and accuracy measurements of FT-ICR MS allow for the correlation of mass spectrometric (MS) data with crude oil American Petroleum Institute (API) gravities, which is a major quality parameter used to guide crude oil refining, and represents a value of the density of a crude oil. The double bond equivalent (DBE) distribution as a function of the classes of constituents, as well as the carbon numbers as measured by the carbon number distributions, were examined to correlate the API gravities of heavy, medium, and light crude oils with molecular FT-ICR MS data. An aromaticity tendency was found to directly correlate the FT-ICR MS data with API gravities, regardless of the ionization technique used. This means that an analysis on the molecular level can explain the differences between a heavy and a light crude oil on the basis of the aromaticity of the compounds in different classes. This tendency of FT-ICR MS with all three techniques, namely, ESI(+), ESI(−), and APPI(+), indicates that the molecular composition of the constituents of crude oils is directly associated with API gravity.


2021 ◽  
Author(s):  
Rukuan Chai ◽  
Yuetian Liu ◽  
Yuting He ◽  
Qianjun Liu ◽  
Wenhuan Gu

Abstract Tight oil reservoir plays an increasingly important role in the world energy system, but its recovery is always so low. Hence, a more effective enhanced oil recovery (EOR) technology is urgently needed. Meanwhile, greenhouse effect is more and more serious, a more effective carbon capture and sequestration (CCS) method is also badly needed. Direct current voltage assisted carbonated water-flooding is a new technology that combines direct current voltage with carbonated water-flooding to enhance oil recovery and CO2 sequestration efficiency, simultaneously. Experimental studies were conducted from macroscopic-scale to microscopic-scale to study the performance and mechanism of direct current voltage assisted carbonated water-flooding. Firstly, core flood experiments were implemented to study the effect of direct current voltage assisted carbonated water on oil recovery and CO2 sequestration efficiency. Secondly, contact angle and interfacial tension/dilatational rheology were measured to analyze the effect of direct current voltage assisted carbonated water on crude oil-water-rock interaction. Thirdly, total organic carbon (TOC), gas chromatography (GC), and electrospray ionization-fourier transform ion cyclotron resonance-mass spectrometry (ESI FT ICR-MS) were used to investigate the organic composition change of produced effluents and crude oil in direct current voltage assisted carbonated water treatment. Through direct current voltage assisted carbonated water-flooding experiments, the following results can be obtained. Firstly, direct current voltage assisted carbonated waterflooding showed greater EOR capacity and CO2 sequestration efficiency than individual carbonated water and direct current voltage treatment. With the increase of direct current voltage, oil recovery increases to 38.67% at 1.6V/cm which much higher than 29.07% of carbonated water-flooding and then decreases, meanwhile, CO2 output decreases to only 35.5% at 1.6V/cm which much lower than 45.6% of carbonated water-flooding and then increases. Secondly, in direct current voltage assisted carbonated water-flooding, the wettability alteration is mainly caused by carbonated water and the effect of direct current can be neglected. While both carbonated water and direct current have evident influence on interfacial properties. Herein, with direct current voltage increasing, the interfacial tension firstly decreases and then increases, the interfacial viscoelasticity initially strengthens and then weakens. Thirdly, GC results indicated that crude oil cracking into lighter components occurs during direct current voltage assisted carbonated water-flooding, with the short-chain organic components increasing and the long-chain components decreasing. Meanwhile, TOC and ESI FT ICR-MS results illustrated that CO2 electroreduction do occur in direct current voltage assisted carbonated water-flooding with the dissolved organic molecules increases and the emergence of formic acid. Conclusively, the synergy of CO2 electrochemical reduction into formic acid in aqueous solution and the long-chain molecules electrostimulation pyrolysis into short ones in crude oil mutually resulted in the enhancement of crude oil-carbonated water interaction. This paper proposed a new EOR & CCS technology-direct current voltage assisted carbonated water-flooding. It showed great research and application potential on tight oil development and greenhouse gas control. More work needs to be done to further explore its mechanism. This paper constructs a multiscale & interdisciplinary research system to study the multidisciplinary (EOR&CCS) problem. Specifically, a series connected physical (Core displacement, Contact angle, and Interfacial tension/rheology measurements) and chemistry (TOC, GS, and ESI FT ICR-MS) experiments are combined to explore its regularity and several physics (Atomic physics) and chemistry (Electrochemistry/Inorganic Chemistry) theories are applied to explain its mechanisms.


2019 ◽  
Author(s):  
Min Cui ◽  
Cheng Li ◽  
Yingjun Chen ◽  
Fan Zhang ◽  
Jun Li ◽  
...  

Abstract. The molecular composition and structure of polar organic matters (POM) in particles emitted from various vessels and excavators were characterized using Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (FT-ICR MS). POM was extracted by purified water and was discussed by elemental composition which was divided into three groups, namely CHO, CHON and S-containing compounds (CHONS and CHOS). The results showed that: (i) CHO (accounting for 49 % of total POM relative peak response) was the most abundant group for all tested off-road engines, followed by CHON (33 %) and CHOS (35 %) for diesel- and HFO (heavy fuel oil)-fueled off-road equipment, respectively. (ii) The abundance and structure of the CHON group in water extracts were different in terms of engine type and load. The fraction of relative peak response of CHON was highest for excavator emissions under the working mode compared to other modes (idling and moving). Furthermore, dinitrophenol and methyl dinitrophenol were the most abundant emission species for excavators with high rated speed, while nitronaphthol and methyl nitronaphthol were more important for low rated speed vessels. (iii) The composition and structure of S-containing compounds was directly influenced by fuel oil characteristics (sulfur content and aromatic ring), with much more condensed aromatic rings in S-containing compounds observed for HFO-fueled vessels, while more abundant aliphatic chains were observed in emissions from diesel equipment. Overall, higher fractions of condensed hydrocarbons and aromatic rings in POM emitted from vessels using HFO caused strong optical absorption capacity. And different structures existing in POM could provide a direction to qualitative and quantities the exact organic compounds as tracers to distinguish the emission from diesel or HFO- fueled off-road engines.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Angelica Bianco ◽  
Laurent Deguillaume ◽  
Nadine Chaumerliac ◽  
Mickaël Vaïtilingom ◽  
Miao Wang ◽  
...  

An amendment to this paper has been published and can be accessed via a link at the top of the paper.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Shuntaro Tsubaki ◽  
Hiroshi Nishimura ◽  
Tomoya Imai ◽  
Ayumu Onda ◽  
Masanori Hiraoka

AbstractThe high growth rate of Ulva seaweeds makes it a potential algal biomass resource. In particular, Ulva meridionalis grows up to fourfold a day. Here, we demonstrated strong carbon fixation by U. meridionalis using 13C stable isotope labelling and traced the 13C flux through sugar metabolites with isotope-ratio mass spectrometry (IR-MS), Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS), 13C-nuclear magnetic resonance spectrometry (13C-NMR), and gas chromatography-mass spectrometry (GC–MS). U. meridionalis was first cultured in 13C-labelled enriched artificial seawater for 0–12 h, and the algae were collected every 4 h. U. meridionalis grew 1.8-fold (dry weight), and the 13C ratio reached 40% in 12 h, whereas 13C incorporation hardly occurred under darkness. At the beginning of the light period, 13C was incorporated into nucleic diphosphate (NDP) sugars in 4 h, and 13C labelled peaks were identified using FT-ICR-MS spectra. Using semiquantitative 13C-NMR measurements and GC–MS, 13C was detected in starch and matrix polysaccharides after the formation of NDP sugars. Moreover, the 14:10 light:dark regime resulted into 85% of 13C labelling was achieved after 72 h of cultivation. The rapid 13C uptake by U. meridionalis shows its strong carbon fixation capacity as a promising seaweed biomass feedstock.


Author(s):  
Hengameh Bayat ◽  
Feng Cheng ◽  
Mostafa Dehghanizadeh ◽  
Nicholas Soliz ◽  
Catherine E Brewer ◽  
...  

2001 ◽  
Vol 79 (5-6) ◽  
pp. 546-551 ◽  
Author(s):  
Ryan P Rodgers ◽  
Christopher L Hendrickson ◽  
Mark R Emmett ◽  
Alan G Marshall ◽  
Mark Greaney ◽  
...  

Petroporphyrin compositional analysis of a heavy crude oil has been realized by isolation and subsequent ESI-FT-ICR mass spectrometric analysis of the porphyrin-containing fractions. Vanadium octaethyl (V=O(II)OEP) and nickel octaethyl (Ni(II)OEP) porphyrin standards were analyzed to determine favorable electrospray ionization conditions and provide insight as to the molecular species present (e.g., adducts, multimers). Standard V=O(II)OEP and Ni(II)OEP solutions revealed the presence of both monomer and dimer species with a greater relative abundance of monomers. In contrast, mass spectral analysis of a porphyrin fraction from Cerro Negro crude oil was dominated by dimeric species. MS3 analysis identified a dioctylphthalate (DOP) contaminant, likely introduced during fractionation of the crude oil. DOP-porphyrin complexes and porphyrin-porphyrin dimers were then identified. Infrared multiphoton dissociation (IRMPD) of dimeric species produced the corresponding monomers with minimal fragmentation. The monomeric petroporphyrins were analyzed to reveal the metal (Ni(II) or V=O(II)), porphyrin type (e.g., etio vs. DPEP), and distribution of alkylation.Key words: petroporphyrin, porphyrin, petroleum, electrospray ionization, mass spectrometry, Fourier transform, ion cyclotron resonance, ICR, FT-ICR, FTMS.


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