The study protocol was reviewed by the Institute of Medicine in September 2010 (Institute of Medicine 2010 ) and was approved by the Institutional Review Board of the NIEHS. The study is overseen by a Scientific Advisory Board and a Community Advisory Board.
Petroleum
It is a primary source of energy and raw material for a wide range of industries, including transportation, manufacturing, and petrochemicals.
Petroleum can be refined into various products such as gasoline, diesel fuel, lubricants, and asphalt.
It is an important global commodity, with its production, distribution, and consumption having significant economic and political implications.
Reserach in the field of petroleum science aims to enhance the efficiency, sustainability, and environmental impact of petroleum exploration, extraction, refining, and utilization.
Key areas of study include geology, engineering, chemistry, and economics related to this vital natural resource.
Petrolemu research is critical for meeting the world's growing energy demands while addressing concerns about climate change and environmental protection.
Most cited protocols related to «Petroleum»
The study protocol was reviewed by the Institute of Medicine in September 2010 (Institute of Medicine 2010 ) and was approved by the Institutional Review Board of the NIEHS. The study is overseen by a Scientific Advisory Board and a Community Advisory Board.
Haematology, biochemistry and biological specimen banking in the COACS
Analysate | |
---|---|
Red blood cells | Haemoglobin |
Red corpuscle count | |
Haematocrit | |
Mean corpuscular volume | |
Mean corpuscular | |
Haemoglobin concentration | |
Red blood cell distribution width | |
White blood cells | White cell count Total count |
Differential count | |
Platelets | Platelets Count |
Mean platelet volume | |
Urea | Urine specific gravity |
Ery | |
Urea nitrogen | |
Uric acid (UA) | |
Creatinine (Cr) | |
Urine protein | |
Liver function tests (plasma) | Alkaline phosphatise |
Alanine transaminase (ALT) | |
Aspartate aminotransferase (AST) | |
Phosphatise Transglutaminase (TG) | |
Liver function tests (serum) | HBsAg |
Anti-HBs | |
HBeAg | |
Anti-HBe | |
Anti-HBc | |
Lipids (plasma) | Total cholesterol (TC) |
Total bilirubin (TBIL) | |
Triglycerides (TG) | |
Low density lipoprotein (LDL) | |
Very Low density lipoprotein (VLDL) | |
General chemistry (plasma) | C-reactive protein |
Homocysteine | |
Steroids | |
Glucose | |
Insulin | |
Glycosylated hemoglobin | |
Bio-specimen banking | |
White blood cells | DNA, RNA extraction and analyses |
Serum | Pedtidome profiling |
Plasma | Glycome |
BioLite (left) and liquified petroleum gas (LPG) (right) cookstoves
Flow chart
Study participants in the LPG arm receive a two-burner LPG stove manufactured in Ghana by the Ghana Cylinder Manufacturing Co. (Accra, Ghana). We chose that particular stove because it is readily available in Ghana, both for the current study and for potential future distribution. Enrolled households also receive timely deliveries of LPG gas at no cost to the participants. GRAPHS leased a 5000-kg LPG tank to ensure continuous supply. If households run low on LPG prior to a scheduled delivery, they can contact their fieldworker and the study will make a special delivery. Control arm participants use their own three-stone traditional stoves for the duration of the trial and will receive one BioLite stove at the end of the study period. All participants receive an insecticide-treated net (ITN).
Community-based fieldworkers visit households every week to check up on the intervention stoves and address any problems. In the control areas the community-based fieldworker visits take place as in the intervention arms, and are framed as checkups on the ITNs.
Most recents protocols related to «Petroleum»
Example 122
To a stirred solution of crude 325 in MeCN (100 mL) under nitrogen at rt, was added dropwise a solution of 2,6-dimethylphenol (1.22 g, 10.0 mmol), triethylamine (4.18 mL, 30.0 mmol), and DABCO (0.112 g, 1.00 mmol) in MeCN over 30 min. The mixture immediately turned deep red at the beginning of addition, and was stirred an additional 90 min after addition was completed. The reaction mixture was concentrated by rotary evaporation, and the residue was redissolved in CHCl3 (300 mL). The solution was washed sequentially with sat. aq. NaHCO3 (1×300 mL) and brine (2×300 mL), dried over Na2SO4, filtered, and concentrated by rotary evaporation to give a crude red oil. Flash chromatography on the Combiflash (330 g column, 5 to 20% EtOAc in hexanes gradient), gave 326 (5.02 g, 85% yield over 2 steps) as an off-white solid foam.
1H NMR (400 MHz, CDCl3) δ 8.20 (d, J=7.4 Hz, 1H), 7.06 (s, 3H), 6.08 (d, J=7.4 Hz, 1H), 5.94 (d, J=15.9 Hz, 1H), 5.02 (dd, J=52.1 Hz, 3.1 Hz, 1H), 4.31 (d, J=13.8 Hz, 1H), 4.32-4.18 (m, 2H), 4.03 (dd, J=13.6 Hz, 2.0 Hz, 1H), 2.13 (s, 6H), 1.15-0.97 (m, 28H).
Example 119
To a stirred solution of 322 (5.30 g, 10.58 mmol) in THF (106 mL) under nitrogen at 0° C., was added a solution of TBAF (1.0 M in THF, 21.17 mL) dropwise via syringe. The mixture was brought to rt and stirred 2 h. Volatiles were removed by rotary evaporation to give a crude yellow oil. The material was taken up in EtOAc and flash chromatography on the Combiflash (330 g column, 0 to 5% MeOH in DCM gradient) gave 2.8 g of mostly purified material as a white solid. This material was dissolved in methanol and immobilized on Celite, then loaded on top of a 10% w/w KF/silica column. Flash chromatography (10% MeOH in EtOAc) gave 323 (1.96 g, 63% yield over 3 steps) as a white solid. 1H NMR analysis showed a 13:1 β:α dr at the C2′position (integration of methyl doublet).
Major isomer 1H NMR (400 MHz, MeOH-d4) δ 8.18 (d, J=8.1 Hz, 1H), 7.04 (d, J=7.6 Hz, 1H), 5.95 (d, J=8.2 Hz, 1H), 3.93 (dd, J=12.2 Hz, 2.1 Hz, 1H), 3.89 (t, J=8.2 Hz, 1H), 2.64 (m, 1H), 0.99 (d, 7.1 Hz, 3H). ES+APCI (70 eV) m/z: [M+HCO2]− 302.9.
Example 4
In order to determine whether both trans-THC and cis-THC existed in crude CBD preparations and also if both were present what the ratio of these were, a further study was undertaken using CBD oil purchased from CBD-oil vendors.
Eight different crude CBD oil preparations were tested and all were found to comprise a mixture of trans-THC and cis-THC. Table 4.1 below details the ratios that were found in these oils.
As Table 4.1 demonstrates the ratio of trans-THC to cis-THC varies within the different crude CBD oil preparations obtained from 2.3:1 to 4.4:1 (trans-THC:cis-THC). These ratios are far removed from the botanically derived purified CBD material defined in the present invention.
Example 1
An Arab light crude oil with an API gravity of 33.0 and a sulfur content of 1.6 wt. % was fractionated in a distillation column to form a light stream and a heavy stream. Properties of the feed crude oil stream and the resulting fractions (based on their percent composition in the crude oil fractions) are given in Table 1 below.
Details of the un-hydrotreated heavy stream are shown below in Table 2, where the heavy stream is designated EX-1(A).
The same Arab light crude oil used in Example 1 was directly cracked in the same cracking reactor and under the same conditions as was used in Example 3(A), results are designated CE-1. Specifically, the temperature was 675° and the TOS was 75 seconds.
As can be seen in Table 4, the combined yields of total light olefins from the present methods are significantly higher than the yields from the comparative methods. Further, each of examples 3(A), 3(B), and 3(Combined) show significantly decreased levels of coke formation relative to the comparative example CE-1.
Example 2
The heavy stream from Example 1 was hydrotreated in a three-stage hydrotreater. The reaction conditions were: a weighted average bed temperature of 400° C., a pressure of 150 bar, a liquid hourly space velocity (LHSV) of 0.5 h−1, an Hz/oil ratio 1200:1(v/v), an oil flowrate of 300 ml/h, and an H2 flowrate of 360 L/h.
The first stage of the hydrotreater used a KFR-22 catalyst from Albemarle Co. to accomplish hydro-demetallization (HDM). The second stage of the hydrotreater used a KFR-33 catalyst from Albemarle Co. to accomplish hydro-desulfurization (HDS). The third stage of the hydrotreater used a KFR-70 catalyst from Albemarle Co. to accomplish hydro-dearomatization (HDA). The first, second, and third stages were discrete beds placed atop one another in a single reaction zone. The heavy stream flowed downward to the first stage, then to the second stage, and then to the third stage. Properties of this hydrotreated heavy stream are shown in Table 2 below and are designated EX-2.
The hydrotreated heavy stream from Example 2 was fed to the advanced cracking evaluation unit. A TOS of 75 seconds, a residence time of from 1 to 2 seconds, and a temperature of 645° C. was used. Characterization of the product is given in Table 5 below.
As can be seen in Table 5, utilizing a hydrotreated heavy stream as the feed to the catalytic reactor results in higher conversion; greater yield of C2, C3, and C4 olefins; greater yield of gasoline; and significantly decreased coke formation, among other advantages.
Example 3
The respective fractions of Arab light crude were cracked at the conditions described below. A catalyst with the composition shown in Table 3 below as used in all of the reactions.
An Advanced Cracking Evaluation (ACE) unit was used to simulate a commercial FCC process. The reaction was run two times with fresh catalyst to simulate two separate FCC reaction zones in parallel.
Prior to each experiment, the catalyst is loaded into the reactor and heated to the desired reaction temperature. N2 gas is fed through the feed injector from the bottom to keep catalyst particles fluidized. Once the catalyst bed temperature reaches within ±2° C. of the reaction temperature, the reaction can begin. Feed is then injected for a predetermined time (time-on-stream (TOS)). The desired catalyst-to-feed ratio is obtained by controlling the feed pump. The gaseous product is routed to the liquid receiver, where C5+ hydrocarbons are condensed and the remaining gases are routed to the gas receiver. After catalyst stripping is over, the reactor is heated to 700° C., and nitrogen was replaced with air to regenerate the catalyst. During regeneration, the released gas is routed to a CO2 analyzer. Coke yield is calculated from the flue gas flow rate and CO2 concentration. The above process was repeated for each of Examples 3(A) and 3(B). The weight ratio of catalyst to hydrocarbons was 8.
It should be understood that time-on-stream (TOS) is directly proportional to residence time.
The light stream from Example 1 was fed to the advanced cracking evaluation unit. A time-on-stream (TOS) of 75 seconds, a residence time of from 1 to 2 seconds, and a temperature of 675° C. was used.
The hydrotreated heavy stream from Example 2 was fed to the advanced cracking evaluation unit. A TOS of 75 seconds, a residence time of from 1 to 2 seconds, and a temperature of 645° C. was used. Characterization is shown in both Table 4 and Table 5.
The streams of Examples 3(A) and 3(B) were combined to form a single stream. The single stream simulates the output of processing a whole crude according to the methods of the present disclosure.
Example 3(Combined) is a weighted average of Examples 3(A) and 3(B). Example 3(A) represented 53 wt. % of Example 3(Combined). Example 3(B) represented 44 wt. % of Example 3 (Combined).
Example 1
An Arab light crude oil with an API gravity of 33.0 and a sulfur content of 1.6 wt. % was fractionated in a distillation column to form a light stream and a heavy stream. Properties of the feed crude oil stream and the resulting fractions (based on their wt. % composition in the crude oil) are given in Table 1 below.
The same Arab light crude oil used in Example 3 was directly cracked in the same cracking reactor and under the same conditions as was used in Example 3.
As can be seen in Table 4, the yield of total light olefins from the inventive EX-3 is significantly higher than the yield of light olefins in the comparative CE-1. Additionally, EX-3 shows significantly lower coke formation than the comparative CE-1.
Example 2
The heavy stream from Example 1 was hydrotreated in a three-stage hydrotreater. The reaction conditions were: a weighted average bed temperature of 400° C., a pressure of 150 bar, a liquid hourly space velocity (LHSV) of 0.5 h−1, an H2/oil ratio 1200:1 (v/v), an oil flowrate of 300 ml/h, and an H2 flowrate of 360 L/h.
The first stage of the hydrotreater used a KFR-22 catalyst from Albemarle Co. to accomplish hydro-demetallization (HDM). The second stage of the hydrotreater used a KFR-33 catalyst from Albemarle Co. to accomplish hydro-desulfurization (HDS). The third stage of the hydrotreater used a KFR-70 catalyst from Albemarle Co. to accomplish hydro-dearomatization (HDA). The first, second, and third stages were discrete beds placed atop one another in a single reaction zone. The heavy stream flowed downward to the first stage, then to the second stage, and then to the third stage. Properties of this hydrotreated heavy stream are shown in Table 2 below.
Example 3
A catalyst with the composition shown in Table 3 below as used in all of the reactions.
An Advanced Cracking Evaluation (ACE) unit was used to simulate a down-flow FCC reaction zone with multiple inlet points. The ACE unit emulates commercial FCC process.
Prior to each experiment, the catalyst is loaded into the reactor and heated to the desired reaction temperature. N2 gas is fed through the feed injector from the bottom to keep catalyst particles fluidized. Once the catalyst bed temperature reaches within ±2° C. of the reaction temperature, the reaction can begin. Feed is then injected for a predetermined time (time-on-stream (TOS)). The desired catalyst-to-feed ratio is obtained by controlling the feed pump. The gaseous product is routed to the liquid receiver, where C5+ hydrocarbons are condensed and the remaining gases are routed to the gas receiver. After catalyst stripping is over, the reactor is heated to 700° C., and nitrogen was replaced with air to regenerate the catalyst. During regeneration, the released gas is routed to a CO2 analyzer. Coke yield is calculated from the flue gas flow rate and CO2 concentration. The above process was repeated for each of Examples 3(A) and 3(B).
The light stream from Example 1 was combined with the hydrotreated heavy stream from Example 2 to form a combined feed stream. The combined feed stream was fed to the ACE unit. A time-on-stream (TOS) of 75 seconds and a temperature of 675° C. was used. Fresh catalyst was steamed deactivated at 810° C. for 6 hours to resemble the equilibrium catalyst in the actual process. The steam deactivated catalyst was used in this reaction. It should be understood that TOS is directly proportional to residence time.
Top products related to «Petroleum»
More about "Petroleum"
It is a crucial global energy source and raw material, with applications spanning transportation, manufacturing, and petrochemicals.
Through refining, petroleum yields a wide range of products, including gasoline, diesel fuel, lubricants, and asphalt.
This vital natural resource has significant economic and political implications, with its production, distribution, and consumption being extensively researched.
Key areas of petroleum science include geology, engineering, chemistry, and economics.
Researchers aim to enhance the efficiency, sustainability, and environmental impact of petroleum exploration, extraction, refining, and utilization.
Synonyms for petroleum include fossil fuel, crude, and mineral oil.
Related terms include hydrocarbons, natural gas, refining, and petrochemicals.
Abbreviations used in the field include API (American Petroleum Institute) and OPEC (Organization of the Petroleum Exporting Countries).
Subtopics in petroleum research span topics such as reservoir characterization, drilling and production techniques, refining processes (e.g., distillation, cracking, reforming), and the environmental impacts of petroleum usage.
Specialized equipment and materials used in petroleum research may include the Inova-400 analytical instrument, Sorvell ST40R centrifuge, and chemicals like toluene, methanol, Alcalase® 2.4 FG, ethanol, chloroform, sodium dodecyl sulfate, and hydrochloric acid.
By leveraging the latest advancements in petroleum science, researchers can address the world's growing energy demands while mitigating concerns about climate change and environmental protection.