Microscopic versus process parameters in heavy-oil upgrading

Author(s):  
V.A. Munoz ◽  
R.J. Mikula ◽  
C. Payette ◽  
W.W. Lam

The transformation of high molecular weight components present in heavy oils into useable liquid fuels requires their decomposition by means of a variety of processes. The low molecular weight species produced recombine under controlled conditions to generate synthetic fuels. However, an important fraction undergo further recombination into higher molecular weight components, leading to the formation of coke. The optical texture of the coke can be related to its originating components. Those with high sulfur and oxygen content tend to produce cokes with small optical texture or fine mosaic, whereas compounds with relatively high hydrogen content are likely to produce large optical texture or domains. In addition, the structure of the parent chemical components, planar or nonplanar, determines the isotropic or anisotropic character of the coke. Planar molecules have a tendency to align in an approximately parallel arrangement to initiate the formation of the nematic mesophase leading to the formation of anisotropic coke. Nonplanar highly alkylated compounds and/or those rich in polar groups form isotropic coke. The aliphatic branches produce steric hindrance to alignment, whereas the polar groups participate in cross-linking reactions.

2015 ◽  
pp. 54-61 ◽  
Author(s):  
A. G. Varekhov ◽  
O. V. Smirnov

The article reviews the world experience of technological diversification in the fuel hydrocarbons production sphere. It is shown that the lost classical technologies, such as coals destructive hydrogenation and coals gasification, are reviving on a new technology basis. Some technological methods of receiving liquid fuels from biomass of various origin are analyzed. The technological schemes of production of biofuels of three generations using a natural vegetable material, various productions wastes, as well as biomass of water organisms as a carbon source are presented. The estimation was made of production outputs and costs of synthetic fuels (dimethyl ether, biodimethyl ether, biodiesel, gasoline and others). The conditions for development of biofuel technologies were formulated.


Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 381 ◽  
Author(s):  
Haigang Hao ◽  
Pengfei Lian ◽  
Juhui Gong ◽  
Rui Gao

Heavy oil will likely dominate the future energy market. Nevertheless, processing heavy oils using conventional technologies has to face the problems of high hydrogen partial pressure and catalyst deactivation. Our previous work reported a novel method to upgrade heavy oil using hydrogen non-thermal plasma under atmospheric pressure without a catalyst. However, the plasma-driven catalytic hydrogenation mechanism is still ambiguous. In this work, we investigated the intrinsic mechanism of hydrogenating heavy oil in a plasma-driven catalytic system based on density functional theory (DFT) calculations. Two model compounds, toluene and 4-ethyltoluene have been chosen to represent heavy oil, respectively; a hydrogen atom and ethyl radical have been chosen to represent the high reactivity species generated by plasma, respectively. DFT study results indicate that toluene is easily hydrogenated by hydrogen atoms, but hard to hydrocrack into benzene and methane; small radicals, like ethyl radicals, are prone to attach to the carbon atoms in aromatic rings, which is interpreted as the reason for the increased substitution index of trap oil. The present work investigated the hydrogenation mechanism of heavy oil in a plasma-driven catalytic system, both thermodynamically and kinetically.


2018 ◽  
Vol 8 (19) ◽  
Author(s):  
Carolyn L. Nanca ◽  
Kimberly D. Neri ◽  
Anna Christina R. Ngo ◽  
Reuel M. Bennett ◽  
Gina R. Dedeles

Background. Polycyclic aromatic hydrocarbons (PAHs) are common environmental contaminants which are highly toxic due to their carcinogenic and mutagenic effects. They are released into the environment by incomplete combustion of solid and liquid fuels, accidental spillage of oils and seepage from industrial activities. One of the promising processes mitigating PAHs is through biodegradation. However, conventional microbiological treatment processes do not function well at high salt concentrations. Hence, utilization of halophilic bacteria should be considered. Objectives. This study aimed to assess the ability of halophilic bacteria isolated from local salt beds in Pangasinan and Cavite, the Philippines, to degrade PAHs pyrene, fluorene and fluoranthene. Methods. Polycyclic aromatic hydrocarbon-tolerant halophilic bacteria collected from two sampling sites were phenotypically characterized, molecularly identified and tested to determine their potential to degrade the PAHs pyrene, fluorene and fluoranthene at a hypersaline condition. Best PAH degraders were then assayed to identify the optimal degradation using such parameters as pH, temperature and PAH concentration. Testing for enzyme degradation was also done to determine their baseline information. Extraction and analysis of degraded PAHs were performed using centrifugation and UV-vis spectrophotometry. Results. Twelve isolates from both collection sites tolerated and grew in culture with selected PAHs. These were identified into four genera (Halobacillus, Halomonas, Chromohalobacter, and Pontibacillus). Selected best isolates in a series of biodegradation assays with the above-mentioned parameters were Halobacillus B (Collection of Microbial Strains (CMS) 1802) (=trueperi) (Gram-positive) for pyrene and fluoranthene, and Halomonas A (CMS 1901) (Gram-negative) for fluorene. Degrader biomass and PAH degradation were invariably negatively correlated. Qualitative tests with and without peptone as a nitrogen source implied enzymatic degradation. Discussion. Polycyclic aromatic hydrocarbons utilized by these halophilic bacteria served as a sole source of carbon and energy. Implications of biodegradation of the two best isolates show that high molecular weight (HMW) (4-ring) pyrene tends to be degraded better by Gram-positive bacteria and low molecular weight (3-ring) fluorene by Gram-negative degraders. Conclusions. Halophilic bacteria constitute an untapped natural resource for biotechnology in the Philippines. The present study demonstrated their potential use in bioremediation of recalcitrant hydrocarbons in the environment. Competing Interests. The authors declare no competing financial interests.


1980 ◽  
Author(s):  
P. P. Singh ◽  
A. Cohn ◽  
P. W. Pillsbury ◽  
G. W. Bauserman ◽  
P. R. Mulik ◽  
...  

Combustion tests on over twelve types of coal derived liquid fuels from the EDS, H-coal, SRC-I and SRC-II processes and three shale oil fuels have been conducted in gas turbine type combustors. Emission measurements were made of Nox, smoke, CO, and unburned hydrocarbons. Combustor wall temperature profiles were measured. The results are correlated with the fuel properties-percent nitrogen, hydrogen and aromaticity. This part of the paper discusses the fuels used in subscale combustion tests along with the test results. A companion paper (Part II) describes the results of full-scale combustor tests and a long term corrosion/deposition test.


Forests ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 640 ◽  
Author(s):  
Richard Hrčka ◽  
Viera Kučerová ◽  
Tatiana Hýrošová ◽  
Vladimír Hönig

The interaction of water and oak wood is common in outdoor expositions and will remain a probable occurrence in the future. New insights into the recognition of a cell wall saturation limit are presented by a double-weighing method at 20 °C. The cell wall saturation limit, as the property of thermally modified oak wood, is significantly influenced by different treatment temperatures (20, 160, 180, 210 and 240 °C) on a 5% alpha level. A significantly higher equilibrium moisture content was reached by thermally modified oak wood at a temperature of 20 °C and relative humidity of 65% after its equilibrium in the water-in-reservoir. Moreover, the results are used in the treatment of woodchips to produce cellulose or decomposition of thermally modified wood to its basic chemical components. The investigated properties of cellulose revealed its relationship with water. The number of water molecules bonded to a cellulose chain was correlated with other measured compositions: average molecular weight, total crystalline index, lateral order index and polydispersity index. Analyses showed that there was a strong negative correlation between lateral order index and average molecular weight. The same was true between total crystalline index and average molecular weight. The rest of the properties were positively correlated with the number of water molecules bonded to glucopyranose. The results revealed the possible regeneration of a wood sorption ability after heat treatment and the stability of cellulose in such process.


Author(s):  
Shazib Z. Vijlee ◽  
John C. Kramlich ◽  
Ann M. Mescher ◽  
Scott D. Stouffer ◽  
Alanna R. O’Neil-Abels

The use of alternative/synthetic fuels in jet engines requires improved understanding and prediction of the performance envelopes and emissions characteristics relative to the behavior of conventional fuels. In this study, experiments in a toroidal well-stirred reactor (TWSR) are used to study lean premixed combustion temperature and extinction behavior for several fuels including simple alkanes, synthetic jet fuels, and conventional JP8. A perfectly stirred reactor (PSR) model is used to interpret the observed behavior. The first portion of the study deals with jet fuels and synthetic jet fuels with varying concentrations of added aromatic compounds. Synthetic fuels contain little or no natural aromatic species, so aromatic compounds are added to the fuel because fuel system seals require these species to function properly. The liquid fuels are prevaporized and premixed before being burned in the TWSR. Air flow is held constant to keep the reactor loading roughly constant. Temperature is monitored inside the reactor as the fuel flow rate is slowly lowered until extinction occurs. The extinction point is defined by both its equivalence ratio and temperature. The measured blowout point is very similar for all four synthetic fuels and the baseline JP8 at aromatic concentrations of up to 20% by volume. Since blowout is essentially the same for all the base fuels at low aromatic concentrations, a single fuel was used to test the effect of aromatic concentrations from 0 to 100%. PSR models of these complex fuels show the expected result that behavior diverges from an ideal, perfectly premixed model as the combustion approaches extinction. The second portion of this study deals with lean premixed combustion of simple gaseous alkanes (methane, ethane, and propane) in the same TWSR. These simpler fuels were tested for extinction in a similar manner to the complex fuels, and behavior was characterized similarly. Once again, PSR models show that the TWSR behaves similar to a PSR during stable combustion far from blowout, but as it approaches blowout and becomes less stable a single PSR no longer accurately describes the TWSR. This work is a step towards developing chemical reactor networks (CRNs) based on computational fluid dynamics (CFD) of the simple gaseous fuels in the TWSR. Ultimately, CRNs are the only realistic way to accurately perform detailed chemical modeling of the combustion of complex liquid fuels.


Química Nova ◽  
2020 ◽  
Author(s):  
Hemmely Severino ◽  
Christiane Pinto ◽  
André Spigolon ◽  
Carlos Mello ◽  
Tais Silva ◽  
...  

Asphaltenes fractions were extracted and purified from three heavy Brazilian oils. Their mass compositions of C, H, N, Ni and V were obtained from elemental analysis and S and O atomic percentages from EDS. The H/C ratios showed high degree of unsaturation, while the O atomic percentages indicated more pronounced biodegradation effects on two samples. Quantitative data on N, Ni, and V and semi-quantitative data on S were related to oils origins. The structural data of asphaltenes were explored by combining Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance (1 H NMR). The oil with the lower degree of biodegradation contained asphaltenes with a lower level of condensed aromatic rings and longer aliphatic chain substituents. The asphaltenes obtained from the two most biodegraded oils showed similarities of polar groups and the presence of carboxylic functions, as well as lower contents of aliphatic substituents. The quality and quantity of occluded hydrocarbons were assessed after the mild oxidation of the separated asphaltenes fractions. It was suggested that the severe biodegradation which altered these structures may also be responsible to affect their occluded hydrocarbons.


Author(s):  
Fareha Asim ◽  
Salma Farooq ◽  
Sheraz Hussain Siddique ◽  
Saira Faisal

Ultra high molecular weight fibre cannot be dyed using conventional dyeing techniques as they are extremely hydrophobic and do not possess any polar groups. Wet etching of the surface was used as the pre-treatment process to improve the dyeability of the Ultrahigh Molecular Weight Polyethylene (UHMWPE) knitted fabric using potassium dichromate and sulphuric acid as etchants. The surface modified fabric was dyed at 130°C using High Temperature (HT) dyeing technique with disperse dye and evaluated in terms of Color Strength (K/S), washing fastness, rubbing fastness, and tenacity. It has been observed that wet etching improved the colour strength substantially with an overall good fastness to washing and rubbing but the tenacity decreased with an increase in etching time.


2019 ◽  
Vol 142 (1) ◽  
Author(s):  
Charles L. Keesee ◽  
Bing Guo ◽  
Eric L. Petersen

Abstract New laminar flame speed experiments have been collected for two alternative liquid fuels. Understanding the combustion characteristics of these synthetic fuels is an important step in developing new chemical kinetics mechanisms that can be applied to real fuels. Included in this study are two synthetic Jet fuels: Syntroleum S-8 and Shell GTL. The precise composition of these fuels is known to change from sample to sample. Since these are low-vapor pressure fuels, there are additional uncertainties in their introduction into gas-phase mixtures, leading to uncertainty in the mixture equivalence ratio. An in-situ laser absorption technique was implemented to verify the procedure for filling the vessel and to minimize and quantify the uncertainty in the experimental equivalence ratio. The diagnostic utilized a 3.39-μm HeNe laser in conjunction with Beer's law. The resulting spherically expanding, laminar flame experiments were conducted over a range of equivalence ratios from φ = 0.7 to φ = 1.5 at initial conditions of 1 atm and 403 K in the high-temperature, high-pressure (HTHP) constant-volume vessel at Texas A&M University. The experimental results show that both fuels have similar flame speeds with a peak value just under 60 cm/s. However, it is shown that when comparing the results from different datasets for these real fuels, equivalence ratio may not be the best parameter to use. Fuel mole fraction may be a better parameter to use as it is independent of the average fuel molecule or fuel surrogate used to calculate equivalence ratio in these real fuel/air mixtures.


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