scholarly journals Effect of Changes in Precipitants Volume Ratios on Heavy Organics Precipitation from Crude Oil at Different Production Locations using binary Mixtures of Aliphatic Hydrocarbons

IARJSET ◽  
2018 ◽  
Vol 5 (1) ◽  
pp. 23-30
Author(s):  
Godwin A. Udourioh* ◽  
Ozioma Achugasim ◽  
I. P. Okoye
1971 ◽  
Vol 11 (03) ◽  
pp. 229-235 ◽  
Author(s):  
Jaime A. Lescarboura ◽  
John D. Culter ◽  
Harry A. Wahl

Abstract A polymeric drag reducer has been tested in an 8-in. diameter crude oil pipeline. The test segment was 28 miles long. At the normal flow velocity in the 8-in. line of about 6 ft/sec, drag reductions of 16, 21 and 25 percent were obtained at polymer concentrations of 300, 600 and 1,000 volume ppm. A series of tests was run to determine the effect of flow velocity on drag reduction. Drag reduction decreased as the flow velocity decreased. An additional test in a 12-in. pipeline, 32 miles long, supported the results obtained in the 8-in. pipeline. In none of the tests did the polymer appear to degrade or lose effectiveness because of turbulent shear in the lines. Tests were run for the polymer and various polyisobutylenes in a 1-in.-ID laboratory pipe polyisobutylenes in a 1-in.-ID laboratory pipe viscometer. These tests covered a range of concentrations and flow velocities. The results obtained in the 1-in. line showed the same general characteristics as those obtained in the large pipelines. An equation is presented that correlates pipelines. An equation is presented that correlates the 8-in. and 12-in data as a function of flow velocity and polymer concentration. Introduction Drag reduction, as defined by Savins, is the increase in pumpability of a fluid caused by the addition of small amounts of additive to the fluid. The mechanism of drag reduction is not well understood. An extensive discussion on the subject is presented by Patterson et al. Drag reduction occurs only in turbulent flow. Despite this limitation, drag reduction has a wide potential application within the oil industry. At present, however, the only extensive use of drag reducers has been in hydraulic fracturing operations. Water-soluble polymers have been effective in reducing horsepower requirements and/or increasing injection rates during treatments. The drag reduction phenomenon has not been used in the pipelining of large quantities of crude oil and of pipelining of large quantities of crude oil and of petroleum products. Little use has been made of petroleum products. Little use has been made of it in hydraulic fracturing with oil base fluids. One of the main reasons for this situation is that until recently very few materials were available to reduce drag in aliphatic hydrocarbons. Several polymers may be used as drag reducers in aromatic polymers may be used as drag reducers in aromatic or chlorinated solvents. However, drag reduction in aliphatic hydrocarbons has been limited to polyisobutylene and crepe rubber. Another reason polyisobutylene and crepe rubber. Another reason is that there have been discouraging predictions about the performance of drag reducers in large pipes. Ram et al. studied polyisobutylenes in pipes. Ram et al. studied polyisobutylenes in small brass tubes (3.15 to 13.7 mm) and concluded that the critical velocities for onset of drag reduction ranged from 8.5 to 14.2 ft/sec. These velocities were considered usually too high for actual pipeline applications. These researchers also concluded that degradation of long-flexible polymeric chains in turbulent flow was an extremely polymeric chains in turbulent flow was an extremely serious problem. Seyer and Metzner concluded that little or no drag reduction can be expected in large tubes using presently available polymer materials. In this paper we present data on a polymer that gives substantial drag reduction in crude and diesel oils in small and large pipes. Some comparative data obtained with high molecular weight polyisobutylenes are also presented. polyisobutylenes are also presented. EXPERIMENTAL FLOW SYSTEMS Two pipelines, both located in Oklahoma, were used in the testing. One of the pipelines is 8.249-in. ID, 28.3 miles long, running from Kingfisher pump station to Orlando pump station. The line was tapped for pressure measurements at both pump stations and at two intermediate points, thus dividing the line into segments at 7.4, 11.8 and 9.1 miles. The flow rate was measured during the first three tests by gauging tanks at Orlando and by turbine flow meters. For the last twelve tests the system was improved by adding two positive displacement flow meters at Orlando. SPEJ P. 229


2021 ◽  
Author(s):  
Hernando P. Bacosa ◽  
Jhonamie Abiner Mabuhay-Omar ◽  
Rodulf Anthony T. Balisco ◽  
Dawin M. Omar ◽  
Chihiro Inoue

Abstract The contamination of the environment by crude oil and its by-products, which mainly composed of aliphatic and aromatic hydrocarbons, is a widespread problem. Biodegradation by bacteria is one of the processes responsible for the removal of these pollutants. This study was conducted to determine the abilities of Burkholderia sp. B5, Ralstonia sp. B1, Pseudomonas sp. T1, and Cupriavidus sp. X5 to degrade binary mixtures of octane (representing aliphatic hydrocarbons) with benzene, toluene, ethylbenzene, or xylene (BTEX as aromatic hydrocarbons) at a final concentration of 100 ppm under aerobic conditions. These strains were isolated from an enriched bacterial consortium (Yabase or Y consortium) that prefer to degrade aromatic hydrocarbon over aliphatic hydrocarbons. We found that B5 degraded all BTEX compounds more rapidly than octane. In contrast, B1, T1 and X5 utilized more of octane over BTX compounds. B5 also preferred to use benzene over octane with varying concentrations of up to 200 mg/l. B5 possesses alkane hydroxylase (alkB) and catechol 2,3-dioxygenase (C23D) genes, which are responsible for the degradation of alkanes and aromatic hydrocarbons, respectively. This study strongly supports our notion that Burkholderia played a key role in the preferential degradation of aromatic hydrocarbons over aliphatic hydrocarbons in the previously characterized Y consortium. The preferential degradation of more toxic aromatic hydrocarbons over aliphatics is crucial in risk-based bioremediation.


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