scholarly journals High Pressure Gas Pipelines: Trends for the New Millennium

2000 ◽  
Author(s):  
M. Mohitpour ◽  
Trent van Egmond ◽  
W. L. Wright
Keyword(s):  
High Pressure ◽  
High Pressures ◽  
New Technology ◽  
Maximum Flow ◽  
Transport Cost ◽  
Cost Of Transport ◽  
Line Pipe ◽  
Capital Costs ◽  
Technical Developments ◽  
High Pressure Pipeline

The end of the 20th century has seen some major developments to the business of pipelines worldwide. In North America and Europe the trend has been toward deregulation of the industry. In other markets the trend has been toward the use of fixed transport cost contracts between shippers and the pipeline company. The net effect of these changes is increased competition in the transport of energy with the resulting requirement to provide the lowest cost of transport. At the same time pipelines need to maintain the traditionally high levels of safety and reliability that customers, the public and regulators have been accustomed to. The pipeline industry has responded to the challenge to reduce costs on a number of fronts. These include the areas of contracting, financing, planning, regulation, market development, and technical developments as well as many other areas. This paper will focus on technical developments that have allowed pipeline companies to reduce the cost of moving large volumes of natural gas at high pressures. Progress that the industry has made in the areas of capital cost reduction will be illustrated by an example of high pressure pipeline design. Capital costs will be compared for five system design pressures that all result in the same maximum flow rate. The optimum high-grade steel will be chosen for each pressure. This will also be compared to costs for using Composite Reinforced Line Pipe (CRLP) a new technology for the pipeline industry.

scholarly journals Full Flow High Pressure Hot Taps: The New Technology and Why It’s Indispensable to Industry

1998 ◽  
Author(s):  
John A. McElligott ◽  
Joe Delanty ◽  
Burke Delanty
Keyword(s):  
High Pressure ◽  
New Technology ◽  
Large Diameter ◽  
Cost Savings ◽  
Pipeline System ◽  
Gas Industry ◽  
The North ◽  
System Integrity ◽  
Pressure Pipeline ◽  
High Pressure Pipeline

The connection of a new pipeline lateral or loop to an existing high pressure pipeline system has always been fraught with high costs and the potential for major system impacts. Pipeline owners and operators have historically had to choose between a traditional cold connection with its high associated costs and a less expensive but more mysterious hot tap. Although the cost savings of a hot tap have always been considerable, they were not always sufficient to justify the risk of complications during the branch weld or hot tap or during the subsequent operation of the system. Despite their extraordinary costs and throughput impacts, the perceived certainties of cold connections were often sufficient to justify their regular use. The recent Kyoto Protocol on Climate Change has resulted in new commitments by the world’s governments to reduce greenhouse gas emissions. For the North American gas industry, these initiatives could result in voluntary compliance objectives, incentive based programs or legislated reforms — any of which will have significant impacts on current practices. TransCanada PipeLines Limited (TransCanada) has successfully managed the risk/reward conundrum and completed more than 700 large diameter (NPS 12 to NPS 30) horizontal high pressure hot taps without incident since 1960. TCPL’s research and development work has enabled it to refine its procedures to the point where it can now complete branch welding and hot tapping work with minimal effects on throughput, negligible emissions and no system integrity impacts. For TransCanada, the direct advantages of a hot tap over a cold connection have resulted in the avoidance of gross revenue losses of $1 million or more per hot tap, no environmental emissions, seamless service and no impacts whatsoever to shippers. TransCanada PipeLines Services Ltd. (TPSL) has further streamlined the supporting field procedures and now provides a complete turn key service to industry.

Peculiarities of high-pressure hydrogen adsorption on Pt catalyzed Cu-BTC metal–organic framework

2021 ◽  
Vol 23 (7) ◽  
pp. 4277-4286
Author(s):  
S. V. Chuvikov ◽  
E. A. Berdonosova ◽  
A. Krautsou ◽  
J. V. Kostina ◽  
V. V. Minin ◽  
...  
Keyword(s):  
High Pressure ◽  
High Pressures ◽  
Hydrogen Adsorption ◽  
Metal Organic Framework ◽  
Pt Catalyst ◽  
Metal Organic ◽  
Pt Catalyzed ◽  
Pressure Hydrogen ◽  
Organic Framework

Pt-Catalyst plays a key role in hydrogen adsorption by Cu-BTC at high pressures.

scholarly journals Crystal and electronic structure engineering of tin monoxide by external pressure

2021 ◽  
Author(s):  
Kun Li ◽  
Junjie Wang ◽  
Vladislav A. Blatov ◽  
Yutong Gong ◽  
Naoto Umezawa ◽  
...  
Keyword(s):  
Phase Transition ◽  
High Pressure ◽  
Band Gap ◽  
High Pressures ◽  
Low Pressure ◽  
Widespread Application ◽  
Space Group ◽  
Tin Monoxide ◽  
High Possibility ◽  
Pressure Phase

AbstractAlthough tin monoxide (SnO) is an interesting compound due to its p-type conductivity, a widespread application of SnO has been limited by its narrow band gap of 0.7 eV. In this work, we theoretically investigate the structural and electronic properties of several SnO phases under high pressures through employing van der Waals (vdW) functionals. Our calculations reveal that a metastable SnO (β-SnO), which possesses space group P21/c and a wide band gap of 1.9 eV, is more stable than α-SnO at pressures higher than 80 GPa. Moreover, a stable (space group P2/c) and a metastable (space group Pnma) phases of SnO appear at pressures higher than 120 GPa. Energy and topological analyses show that P2/c-SnO has a high possibility to directly transform to β-SnO at around 120 GPa. Our work also reveals that β-SnO is a necessary intermediate state between high-pressure phase Pnma-SnO and low-pressure phase α-SnO for the phase transition path Pnma-SnO →β-SnO → α-SnO. Two phase transition analyses indicate that there is a high possibility to synthesize β-SnO under high-pressure conditions and have it remain stable under normal pressure. Finally, our study reveals that the conductive property of β-SnO can be engineered in a low-pressure range (0–9 GPa) through a semiconductor-to-metal transition, while maintaining transparency in the visible light range.

scholarly journals The thermal conductivity of the Earth's core and implications for its thermal and compositional evolution

2020 ◽  
Author(s):  
Kenji Ohta ◽  
Kei Hirose
Keyword(s):  
Thermal Conductivity ◽  
High Pressure ◽  
Thermal History ◽  
Diamond Anvil Cell ◽  
High Pressures ◽  
Iron Alloys ◽  
Compositional Evolution ◽  
The Earth ◽  
Diamond Anvil ◽  
High Pressures And Temperatures

Abstract Precise determinations of the thermal conductivity of iron alloys at high pressures and temperatures are essential for understanding the thermal history and dynamics of the metallic cores of the Earth. We review relevant high-pressure experiments using a diamond-anvil cell and discuss implications of high core conductivity for its thermal and compositional evolution.

On the Negative Excess Isotherms for Methane Adsorption at High Pressure: Modeling and Experiment

SPE Journal ◽  
2019 ◽  
Vol 24 (06) ◽  
pp. 2504-2525 ◽  
Author(s):  
Jing Li ◽  
Keliu Wu ◽  
Zhangxin Chen ◽  
Kun Wang ◽  
Jia Luo ◽  
...  
Keyword(s):  
High Pressure ◽  
Mass Balance ◽  
High Pressures ◽  
Pore Wall ◽  
Void Volume ◽  
Excess Adsorption ◽  
Experimental Conditions ◽  
Accessible Volume ◽  
Adsorbed Phase

Summary An excess adsorption amount obtained in experiments is always determined by mass balance with a void volume measured by helium (He) –expansion tests. However, He, with a small kinetic diameter, can penetrate into narrow pores in porous media that are inaccessible to adsorbate gases [e.g., methane (CH4)]. Thus, the actual accessible volume for a specific adsorbate is always overestimated by an He–based void volume; such overestimation directly leads to errors in the determination of excess isotherms in the laboratory, such as “negative isotherms” for gas adsorption at high pressures, which further affects an accurate description of total gas in place (GIP) for shale–gas reservoirs. In this work, the mass balance for determining the adsorbed amount is rewritten, and two particular concepts, an “apparent excess adsorption” and an “actual excess adsorption,” are considered. Apparent adsorption is directly determined by an He–based volume, corresponding to the traditional treatment in experimental conditions, whereas actual adsorption is determined by an adsorbate–accessible volume, where pore–wall potential is always nonpositive (i.e., an attractive molecule/pore–wall interaction). Results show the following: The apparent excess isotherm determined by the He–based volume gradually becomes negative at high pressures, but the actual one determined by the adsorbate–accessible volume always remains positive.The negative adsorption phenomenon in the apparent excess isotherm is a result of the overestimation in the adsorbate–accessible volume, and a larger overestimation leads to an earlier appearance of this negative adsorption.The positive amount in the actual excess isotherm indicates that the adsorbed phase is always denser than the bulk gas because of the molecule/pore–wall attraction aiding the compression of the adsorbed molecules. Practically, an overestimation in pore volume (PV) is only 3.74% for our studied sample, but it leads to an underestimation reaching up to 22.1% in the actual excess amount at geologic conditions (i.e., approximately 47 MPa and approximately 384 K). Such an overestimation in PV also underestimates the proportions of the adsorbed–gas amount to the free–gas amount and to the total GIP. Therefore, our present work underlines the importance of a void volume in the determination of adsorption isotherms; moreover, we establish a path for a more–accurate evaluation of gas storage in geologic shale reservoirs with high pressure.

scholarly journals Gaseous combustion at high pressures. —Part X. The co-volume corrections, maximum temperatures and dissociation of steam and carbon dioxide in explosions

1928 ◽  
Vol 119 (782) ◽  
pp. 464-480
Keyword(s):  
Carbon Dioxide ◽  
High Pressure ◽  
Internal Energy ◽  
High Temperatures ◽  
High Pressures ◽  
Internal Combustion ◽  
Systematic Survey ◽  
Explosion Method ◽  
Maximum Temperatures ◽  
Very High

During the researches upon high-pressure explosions of carbonic oxide-air, hydrogen-air, etc., mixtures, which have been described in the previous papers of this series, a mass of data has been accumulated relating to the influence of density and temperature upon the internal energy of gases and the dissociation of steam and carbon dioxide. Some time ago, at Prof. Bone’s request, the author undertook a systematic survey of the data in question, and the present paper summarises some of the principal results thereof, which it is hoped will throw light upon problems interesting alike to chemists, physicists and internal-combustion engineers. The explosion method affords the only means known at present of determining the internal energies of gases at very high temperatures, and it has been used for this purpose for upwards of 50 years. Although by no means without difficulties, arising from uncertainties of some of the assumptions upon which it is based, yet, for want of a better, its results have been generally accepted as being at least provisionally valuable. Amongst the more recent investigations which have attracted attention in this connection should be mentioned those of Pier, Bjerrum, Siegel and Fenning, all of whom worked at low or medium pressures.

scholarly journals Annealing of Al-Zn-Mg-Cu Alloy at High Pressures: Evolution of Microstructure and the Corrosion Behavior

Materials ◽  
2021 ◽  
Vol 14 (8) ◽  
pp. 2076
Author(s):  
Chuanjun Suo ◽  
Pan Ma ◽  
Yandong Jia ◽  
Xiao Liu ◽  
Xuerong Shi ◽  
...  
Keyword(s):  
High Pressure ◽  
High Pressures ◽  
Electrochemical Impedance ◽  
Extrusion Direction ◽  
Corrosion Properties ◽  
Cu Alloy ◽  
The Matrix ◽  
Annealing Pressure ◽  
Corrosion Pits ◽  
Evolution Of Microstructure

Extruded Al-Zn-Mg-Cu alloy samples with grains aligned parallel to the extrusion direction were subjected to high-pressure annealing. The effects of annealing pressure on the microstructure, hardness, and corrosion properties (evaluated using potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS)) were investigated. Phase analysis showed the presence of MgZn2 and α-Al phases, the MgZn2 phase dissolved into the matrix, and its amount decreased with the increasing annealing pressure. The recrystallization was inhibited, and the grains were refined, leading to an increase in the Vickers hardness with increasing the annealing pressure. The corrosion resistance was improved after high-pressure treatment, and a stable passivation layer was observed. Meanwhile, the number of corrosion pits and the width of corrosion cracks decreased in the high-pressure annealed samples.

Chemistry, Physical Nature, and Rheology of Aqueous Stimulation Foams

1981 ◽  
Vol 21 (04) ◽  
pp. 410-414 ◽  
Author(s):  
David L. Holcomb ◽  
Ed Callaway ◽  
Lynn L. Curry
Keyword(s):  
High Pressure ◽  
Surfactant Concentration ◽  
High Pressures ◽  
Foam Stability ◽  
Streaming Potential ◽  
Physical Nature ◽  
Chemical Additives ◽  
Laboratory Equipment ◽  
Foaming Agent ◽  
Fracturing Fluids

Abstract Laboratory equipment has been designed specificallyto study effectively the microscopic structure offlowing foams at high pressures. In addition, application of foaming-agent optimization techniquesto design stable foams at varying foam qualities isdemonstrated at high pressures - i.e., 500 to 2,000psig (3448 to 13 792 kPa). Capillary viscosity datafor these foams is established and correlated with avideo-photomicroscopic study of the flowing foamand their designated bubble qualities. Foaming-agent screening information from the tests is providedindicating the foaming-agent generic chemistry thatallows optimal foam stability under high-pressure conditions. Introduction The study of contemporary foam rheology has arather interrupted history beginning with Fried'swork in 1961 on a foam drive process, which was followed by Raza and Marsden's 1965 paper onrheology and streaming potential. During 1969Blauer et al. studied foam flow properties andmade successful comparisons of data obtained incapillary viscometer tests and actual oilfield tubulardata. These investigations lead to the development ofdata and calculated procedures for using high-qualityfoams as fracturing fluids to transport proppanteffectively with extremely low formation damage as aresult of smaller amounts of water or liquid incontact with the formation. With all the theoretical depiction of flowing foamstructure, it was felt that a study was needed to showvisually the actual flowing foam under pressure. Thiswas undertaken in a study' where oil-foamingsurfactant concentrations were optimized using anapparatus similar to ours. (The majority of foamstimulation treatments use aqueous bases, and thisstudy was conducted exclusively with them.) The goal of this project was to design equipmentthat could be adapted to a TV camera/microscopesystem to allow videotaping of flowing foam in aview cell under pressure. To study effectively thechemical nature of four different surfactant foams, the temperature was kept at 80 deg. F (26.7 deg. C)throughout the study. Also, one foam quality of88%, or 88% nitrogen and 12% water was chosenusing 2% KCl water as the liquid phase. Selected pictures from the videotape are presented to show thesuccession of bubble-structure change with pressure.In addition, the effect of surfactant concentration (which had been thought to play a small role, if any, in the rheology of foams) is shown. This allows aneven greater ability to optimize surfactant concentration in the production of stable foams forstimulation. The subjective bubble-quality scale of Holcomb etal. is refined by showing the average bubblediameters at various study pressures and is demonstrated photographically in Figs. 1 through 3.For the viscosity tests through the capillaryviscometer system, a constant 1,000-psi input pressure was maintained for the generation of foam. Testing Apparatus, Procedure, and Chemical Additives The high-pressure test apparatus was designed tomeet the rate requirements for a laboratory testsample of 700 cm (liquid) or more. The system iscapable of pressures to 3,000 psi (20 683 kPa). The pump is a Williams Oscillamatic TM single-strokemodel with a pressure rating to 10,000 psi (68 946kPa). All main lines are 6.35 mm in diameter. Trunklines to the gauges are 3.175-mm-diameter tubing.All tubing in the apparatus is 316 stainless steel. (SeeFig. 4.) SPEJ P. 410^

Welding Stress Numerical Simulation and Analysis of High-Pressure Pipeline

2014 ◽  
Vol 912-914 ◽  
pp. 890-894
Author(s):  
Lei Zhang ◽  
Jin Zhou Zhang ◽  
Xiao Ming Li
Keyword(s):  
High Pressure ◽  
Welding Process ◽  
Source Model ◽  
Heat Source Model ◽  
Welding Stress ◽  
Welding Temperature ◽  
Welding Arc ◽  
Pressure Pipeline ◽  
Pipeline Welding ◽  
High Pressure Pipeline

Welded stress has an important impact on quality and life of of high-pressure pipeline. Based on pipeline material performance, considered welding arc force and its mining action, selected double ellipsoidal heat source model, simulated welding process of of high-pressure pipeline, analysised welding temperature field and stress field, determined the distribution disciplines of welding stress, provides useful help on exploring the disciplines of pipeline welding.

Crystal Field Analysis of the Magnetization Curves of HoFe11Ti under High Pressure

2013 ◽  
Vol 818 ◽  
pp. 72-76 ◽  
Author(s):  
Gang Su
Keyword(s):  
High Pressure ◽  
Hydrogen Atom ◽  
Electric Field ◽  
Single Crystals ◽  
High Pressures ◽  
Field Analysis ◽  
Magnetization Curves ◽  
Crystalline Electric Field ◽  
Crystalline Anisotropy ◽  
Magneto Crystalline Anisotropy

The crystalline electric field parameters Anmfor HoFe11Ti under different pressures were evaluated by fitting calculations to the magnetization curves measured on the single crystals at several temperatures. It was found that magneto-crystalline anisotropy has been changed by high pressure and the Anmfor HoFe11Ti under high pressures are strikingly different from Anmfor the corresponding HoFe11Ti H with interstitial hydrogen atom.

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