GB2226520A - Extruding a continuous polymeric encapsulant of varying composition over a metal line - Google Patents
Extruding a continuous polymeric encapsulant of varying composition over a metal line Download PDFInfo
- Publication number
- GB2226520A GB2226520A GB8928062A GB8928062A GB2226520A GB 2226520 A GB2226520 A GB 2226520A GB 8928062 A GB8928062 A GB 8928062A GB 8928062 A GB8928062 A GB 8928062A GB 2226520 A GB2226520 A GB 2226520A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymer
- selected polymer
- line
- metal line
- encapsulant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000008393 encapsulating agent Substances 0.000 title claims abstract description 36
- 239000000203 mixture Substances 0.000 title claims abstract description 35
- 239000002184 metal Substances 0.000 title claims abstract description 32
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 32
- 229920000642 polymer Polymers 0.000 claims abstract description 125
- 239000004677 Nylon Substances 0.000 claims abstract description 32
- 229920001778 nylon Polymers 0.000 claims abstract description 32
- 239000002131 composite material Substances 0.000 claims abstract description 28
- 229920002313 fluoropolymer Polymers 0.000 claims abstract description 20
- 239000004811 fluoropolymer Substances 0.000 claims abstract description 20
- 239000012530 fluid Substances 0.000 claims abstract description 17
- 238000002844 melting Methods 0.000 claims abstract description 6
- 230000008018 melting Effects 0.000 claims abstract description 6
- 238000001125 extrusion Methods 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 18
- 238000000354 decomposition reaction Methods 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 238000002347 injection Methods 0.000 abstract description 29
- 239000007924 injection Substances 0.000 abstract description 29
- 239000000463 material Substances 0.000 abstract description 29
- 239000000126 substance Substances 0.000 abstract description 7
- 238000002425 crystallisation Methods 0.000 abstract description 2
- 238000004391 petroleum recovery Methods 0.000 abstract description 2
- 229920001780 ECTFE Polymers 0.000 description 15
- 238000005538 encapsulation Methods 0.000 description 7
- 239000002861 polymer material Substances 0.000 description 7
- 230000035882 stress Effects 0.000 description 7
- 238000005336 cracking Methods 0.000 description 5
- 230000008859 change Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 229920002292 Nylon 6 Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 235000012438 extruded product Nutrition 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229920006051 Capron® Polymers 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- QZPSXPBJTPJTSZ-UHFFFAOYSA-N aqua regia Chemical compound Cl.O[N+]([O-])=O QZPSXPBJTPJTSZ-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B17/00—Drilling rods or pipes; Flexible drill strings; Kellies; Drill collars; Sucker rods; Cables; Casings; Tubings
- E21B17/10—Wear protectors; Centralising devices, e.g. stabilisers
- E21B17/1042—Elastomer protector or centering means
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/15—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor incorporating preformed parts or layers, e.g. extrusion moulding around inserts
- B29C48/151—Coating hollow articles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/36—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
- B29C48/49—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using two or more extruders to feed one die or nozzle
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Mining & Mineral Resources (AREA)
- Physics & Mathematics (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The metal line is suitable for transmitting signals or injection of chemicals in a hostile subterranean environment. The encapsulant is continuously extruded as sequential sections, comprising a first nylon-based material section and a second fluoropolymer-based material section, and an intermediate section wherein the composition of the encapsulant is a composite of varying percentages of the nylon and fluoropolymer-based materials. The metal line is preheated so that the extruded polymer does not stress crack, and the composite material is extruded at a temperature substantially above the melting point of nylon. and is fluid cooled to delay crystallisation. The encapsulated tubular metal line is suited for transmitting fluid through a petroleum recovery well bore having a corrosive fluid wherein the temperature in the well bore varies with depth. The continuous extrusion between the different sections, avoids the leakage that might otherwise occur, between seals at the section junctions.
Description
DESCRIPTION
EXTRUDED VARIABLE ENCAPSULATED SUBSURFACE LINE
AND METHOD
The present invention relates to elongate lines with extruded encapsulants and, more particularly, to techniques for continously extruding an encapsulant over a metal line suitable for subsurface -signal transmission or chemical injection.
Encapsulated lines have long been used for transmitting fluid, fluid pressure or electrical signals through hostile environments to subsurface locations. In the petroleum recovery industry, for example, it is common to provide a metal injection line secured to the exterior of tubing as the tubing is lowered into a well bore. The injection line may be used to transmit from the surface to one or more downhole tools, and may also be used to inject a desired chemical into the formation to enhance recovery of well fluids. To minimise the rupture of the injection line over a period of time due to corrosion and/or abrasion of the downhole fluids, such injection lines have long been covered with a selected polymer, such as nylon.This encapsulating material is typically applied by extruding the nylon on the metal injection line, so that the nylon sufficiently covers the exterior of the metal injection line.
As geologists search deeper into the earth for hydrocarbons, the temperature of the well bore and thus the temperature to which the injection line is subjected generally tend to increase. Moreover, it is frequently known that certain sections of a well bore will be subjected to one type of fluid environment, while another section is subjected to a more hostile environment. Accordingly, one type of polymer may be ideally suited as the encapsulant for an upper! less corrosive section of the well bore, while another type of polymer is ideally suited as the encapsulant for a lower, higher temperature section of the well bore. One polymer used for "deep well" injection lines is a fluoropolymer! which exhibits high chemical resistance and good barrier properties.
The problem, however, remains with providing a reliable seal between the different material encapsulants for different sections of a subterranean injection line. Since the injection line is typically continuous from the surface to the selected depth in the well bore, a leak along any portion of the injection line practically results in failure of the entire injection line. The cost of repairing the injection line at this point of the leak is negligible compared to the cost of retrieving and reinserting the injection line in the well borer and the cost of the resultant delay in production of hydrocarbon from the formation. Any seal between different material encapsulants for an injection line must therefore be fluid-tight to prevent well fluids from contacting the metal injection line over a prolonged period of time.Moreover! any seal between these different encapsulants generally cannot have a diameter significantly greater than the diameter of the encapsulated injection line. An expanded diameter section of the encapsulated line will typically be quickly worn as the injection line and the tubing are lowered into the well! and may cause a downhole "hang-up" which in turn causes lost time and expense.
As a result of the disadvantage and problems associated with providing a reliable seal between two different encapsulating polymers on a single injection line, the prior art has long selected the polymer for an injection line which is best able to withstand the most hostile environment conditions to which any section of the injection line will be subjected. In other words, while a nylon material encapsulant might be ideal for the upper 5,000 feet of a bore hole and a fluoropolymer encapsulant suitable for the lower 5,000 feet of a bore hole, the prior art has typically selected the more heat stable and heat and chemical resistant fluoropolymer as the encapsulant for the entire 101000 feet of injection line.This "single polymer" selection accordingly results in substantially increased costs for the encapsulated injection line, since a suitable fluoropolymer encapsulant is typically much more expensive than a suitable nylon encapsulant.
Moreover, this single polymer" selection may result in the use of material for the encapsulant of a portion of the injection line which is not well suitable for the environment in which that section of the injection line is positioned.
The disadvantages of the prior art are overcome by the present invention, and an improved variable composition encapsulant and method of forming the encapsulant on a line suitable for subsurface use are hereinafter disclosed.
According to a first aspect of the present invention, a method of encapsulating an elongate metal line suitable for positioning in a subsurface well comprises extruding a first-selected polymer circumferentially about a first section of the line having a preselected length; extruding a second-selected polymer circumferentially about a second section of the line having a predetermined length; and extruding a composite polymer circumferentially about an intermediate section of the line between the first and second sections, the composition of the composite polymer varying along the intermediate length of the line from a high first-selected polymer/low second-selected polymer composition to a low first-selected polymer/high second-selected polymer composition, such that a continuous extruded encapsulant is formed interconnecting the first- and second-selected polymers, and substantially no part of the extruded mixture having substantially equal proportions of the first- and second-selected polymers.
The encapsulant is continuously extruded about the metal line, whether it be a fluid conduit or an electric conductor to produce no discernible material change interfaces.
Preferably, the first-selected polymer is a nylon-based polymer and the second-selected polymer is a fluoropolymer-based polymer.
Also, the composition of the composite polymer may vary uniformly with the length of the intermediate section.
The metal line is preferably heated before applying the nylon/f luoropolymer material, thereby reducing the likelihood of stress cracks subsequently developing in this extruded section. The temperature of the extruded composite material varies according to a preferred technique wherein the nylon is heated to a temperature above its melting points but below its decomposition point, and the fluoropolymer is heated to a temperature just slightly in excess of its melting point. The composite material is preferably cooled in the air to delay crystallisation of the composite polymer.
According to a second aspect of the present invention an encapsulated metal line suitable for positioning in a hostile subsurface environment! comprises a first-selected polymer encapsulant circumferentially positioned about a first length of the line; a second-selected polymer encapsulant circumferentially postioned about a second length of the line; and! a composite polymer circumferentially positioned about an intermediate section of the line between the first and second lengths'. the composition of the composite polymer varying along the intermediate length from a high first-selected polymer/low second-selected polymer composition to a low first-selected polymer/high second-selected polymer composition! such that a continuous encapsulant is formed interconnecting the first- and second-selected polymer encapsulants, and substantially no part of the extruded mixture having substantially equal proportions of the first- and second-selected polymer.
A feature of the present invention is that a reliable encapsulant may be applied to protect the entire length of a metal line to be positioned in different environments along its length! such that a selected material for the encapsulant can be based on the differing anticipated conditions along the length of the line! thereby substantially reducing the cost of providing a suitable encapsulated line.
An advantage of the present invention is that the encapsulated line can constitute a metal tubing suitable for use as an injection line in a subterranean well bore. The intermediate section of the encapsulant does not increase the diameter of the injection line so that problems associated with excessive wear of an enlarged diameter encapsulated section and with hang-ups in a well bore are avoided.
These and other objects! features! and advantages of the present invention will become apparent from the following detailed description.
The first selected polymer, which is extruded circumferentially about a line, such as copper, stainless steel or other fluid conducting tubing! or electrical wire, will be nylon-based. Preferably, such nylon will be modified nylon 6r which is an extrusion grade resin for tubing applications.
Typical of such nylon 6 materials, in modified form, is a heat stabilised CAPRON 8254 HS, of Allied
Plastics, Morristown, New Jersey. Typically, the selected nylon for use in the present invention will have the typical properties shown in Table 1.
The second selected polymer will be a fluoropolymer based material which is derivative - of a fluoropolymer resin. Preferably, the selected fluoropolymer utilised as the second polymer will have key properties approximating or equal to those shown in Table 2.
Such a fluoropolymer resin material is marketed under the trademark HALAR by Ausimont, Morristown, New Jersey. A particular fluoropolymer resin is marketed under the trademark HALAR-ECTFE, having the physical properties shown in Table 3.
In the present invention the first and second polymer materials are extruded into the metal line to form three basic coatings. The first coating, for lower temperature usage, will be made of the first selected polymer, followed by a length of composite polymer which will be a combination of varying percentages of the nylon-based polymer material and a fluoropolymer-based material. The third coating for high temperature exposure will be the fluoropolymerbased material. In preparing the metal line for encapsulation, an extruder system may be utilised.
Such a system is well known to those skilled in the art, and comprises a device with a rotating screw turning inside a heated barrel. The screw is rotated by an external drive and the barrel of the extruder is heated by electric heating units, usually with three or more of the variable temperature units located along the barrel. The screw enters one end of the extruder barrel while the opposite end is fixed with an extrudate head and die. The die can be variable in design! dependent upon the particular diameter and lengths of the lines to be encapsulated in the present process. The head and die area also are heated. At the open end of the barrel! a material hopper is located above the rotating screw to allow introduction of the various types of materials to be extruded.
The temperature ranges for the extrusion- of the first and second selected polymers are as shown in
Table 4.
In the encapsulation method of the present invention the extrusion process requires that the actual temperatures be in the upper range for the first selected polymer, above, and in the lower range for the second selected polymer, above. As encapsulation extends from the first selected polymer through the composite polymer, which is a combination of the first and second polymers, to the second polymer, the temperatures in each zone may be adjusted by increasing or decreasing the temperatures, depending upon which polymer is the predominant component in the composite polymer.
In order to obtain optimum properties for encapsulation, the extruded polymer material on the line should be air cooled for such time as the extrudate has solidified to the point of not being deformed or imprinted by light finger pressure, or a minimum of about 60 seconds, whichever is longer.
Thereafter! the encapsulated liner may be water and/or air cooled.
Prior to initiation of encapsulation, the selected line should be pre-heated before entering the die head. Such pre-heating should be performed at a temperature of from between about 3000F and about 4000F in order to help ensure that the extrudate does not crystallise too rapidly, thus causing high stress areas which are subject to fracture after cooling and re-heating.
Prior to performing the encapsulation method, any selected encapsulation materials which may be hygroscopic must be dried. The extruder and extruder barrel are preheated to the processing temperatures desired, as described above. The material to extrude is purged through the barrel to ensure that no contamination of previously processed material occurs. The line is then loaded in the delivery system and assembled into the die. The extruder screw is rotated and the extrudate is allowed to fill the screw, barrel and die head until a consistent melt is achieved. A take-up mechanism is started to pull the line through the die. The screw rpm rotation is increased to create and maintain the desired dimensions and configuration of the extruded product. Thereafter, the material is cooled and the extruded product is wound on a take-up reel, or other device, for storage purposes.
In order to determine the effects of increase in volume, if any, and hardness variations of lines encapsulated using the present process, stainless steel lines were coated with a nylon-based polymer as the first selected polymer and a HALAR material as the fluoropolymer-based composition of the second selected polymer, with a section of the encapsulated line forming a composite of each of these polymers in varying percentages. The length of encapsulated line was exposed for 160 hours at 3000F in No. 2 diesel fuel containing an acid corrosion inhibitor. Another test was run for 504 hours, 2500F with an acid corrosion inhibitor. The samples were collected from regions of the encapsulated line marked as 100% first selected polymer; 90% first selected polymer/10% second selected polymer; 50% first selected polymer; 508 second selected polymer; 10% first selected polymer/90% second selected polymer; and 100% second selected polymer. Three samples from each region were cut with lengths being between 1-1/2 to 2-1/2 inches. All samples were weighed! measured for hardness, placed on a fixture and immersed in the diesel/inhibitor blend for the specified time and temperature. After the specified aging, the fixture was removed cooled to ambient temperatures, the samples removed, and again weighed and measured for hardness. The results of the 160 hour test are set forth in Table 5.
The above test indicated that the second selected polymer material showed stress cracking, which was surprising! because such material should have higher temperature capability. Such cracks appeared along each line sample and seemed to initiate from the line to the o.d. The composite polymer section'. formed of 50% of each of the first and second selected polymers appeared not to be homogeneous and each of the selected polymers had formed distinct domains of the separate materials.
while the 50/50 blend of the first and second polymers forming the composite polymer material appeared firbrous in nature it had not split or separated in any way. The hardness change and volume change of the composite material was well within tolerance.
The same test, as above described'. was performed, but the time was increased to 504 hours.
The results of this test are set forth in table 6.
It should be noted that the method utilised to encapsulate the line with the first and second polymer materials in the above test did not incorporate the pre-heating of the line. The pre-heating step is not necessarily essential, depending upon the percentages of the composite polymer formed from the first and second polymer materials utilised on the line, and taking into consideration the physical and chemical characteristics which will be found in the environment in which the line is used. When the line is pre-heated! as described above, such cracking is effectively eliminated. A test of an encapsulated line encapsulated as above and tested as above described was tested after 160 hours in the test parameters described above. The results of this test are set forth in Table 7.
The above tests indicate that blends formed from 50% nylon-based polymer and 50% fluoropolymer are not acceptable as encapsulants for lines.
Therefore, when practising the present invention, care should be taken to avoid blends with such approximate ranges.
It would be acceptable for the extruded mixture to have a vertically changing composition from substantially 90% of the first-selected polymer and substantially 10% of the second-selected polymer in its upper portions to substantially 90% of the second-selected polymer and substantiaaly 10% of the first-selected polymer in its lowermost portions.
TABLE 1
TYPICAL PROPERTIES OF SELECTED MODIFIED NYLON 6
Property Value
Specific Gravity 1.08
Yield Tensile Strength, psi 5,300
Ultimate Elongation, % 240
Flexural Strength, psi 4,200
Flexural Modulus, psi 110,000
Notched Izod Impact, ft-lbs/in 6.0
Heat Deflection Temp. @ 264 psi, ~F 131
Melting Point, ~F 420
Melt Index (Condition 0, gms/l0 min) 3-6
TABLE 2
Mechanical Properties
Tensile strength - at yield, psi 4500
at break, psi 7000
Elongation at break, % 200
Flexural modulus, psi 240,000
Impact resistance, ft-lbs/in
Izod, notched, 73 F (23 C) no break -400F (-40iC) 2 - 3
Electrical Properties
Dielectric strength, 0.001 in. thick, V/mil 2000
1/8 in. thick, V/mil 490
Dielectric constant, at 60 Hz 2.6 at 103 Hz 2.5
at 106 Hz 2.5
Dissipation factor, at 60 Hz < 0.0009
at 103 Hz 0.0005
at 106 Hz 0.0003
Chemical Resistance, 212 F (100 C)
Sulfuric acid, 600Be no attack
98% no attack
Nitric acid, concentrated no attack
Aqua regia no attack
Sodium hydroxide, 50% no attack
Flammability
Oxygen Index, 1/16" 60
UL 94 vertical, 0.007" 94 V-O Thermal Properties
Melting Point 240~C (464F) Brittleness temperature < -76 C(-105 F)
Maximum service temperature 150-170 C(300-340 ~F)
Heat distortion temperature
under load (ASTM-D-648) 66 psi stress llS'C (240F) 264 psi stress 76eC (170F) Other Properties
Radiation resistance 2 x 10 rads
Weathering resistance, 3000 hr
in weather-ometer no change in properties
Specific gravity 1.68
Moisture Absorption % < 0.1%
Processing
Stock temperature 500 -540 F (260-280 C)
Mold (linear) shrinkage, in/in 0.02-0.025 TABLE 3
TENSILE AND FLEXURAL PROPERTIES AT 730F (23 C)1
HALARE
Property Fluoropolymer
Tensile strength
at yield, psi 4,500
at break, psi 7,000
Elongation
at yield, 1 5
at break, % 200
Flexural yield strength,
psi 7,000
Modulus
Tensile, psi 240,000
Flexural, psi 240,000 (1)ASTM D 638 and D 790 TABLE 4
Melt Temp. Melt Press.Barrel Tenperatures, F material e Die exit e Die psi Rear Middle Front Die 1st Selected 480-510 F 500-2,000 400 to 460 to 455 to 440 to
Polymer 550 530 530 530 2rd Selected 485-560 F 1,000-3,000 410 to 450 to 480 to 480 to
Polymer 550 520 560 560
TABLE 5
Material Volume Hardness Physical
Chg. Chg. Chg.
100% Nylon + .2t + S pts. None
90% Nylon/10% Halar +1.4% -4 pts. None
50% Nylon/50% Halar +2.28 -10 pts. None 108 Nylon/ 0% Halar +1.1% - 7 pts. Stress Cracked 100% Halar +1.2S - 6 pts. Stress Cracked
TABLE 6 Material Volume Hardness Physical 1008 Nylon +1.6S + 5 pts. None 90% Nyl E/lOS Halar +2.0% - 8 pts. Very Minor Crack 50s Nylon/50% Halar +4.0% -13 pts. Extensive Cracking 10% Nylon /90% Halar +2.6% - 7 pts. Extensive Cracking 100% Halar Not Measurable Not Measurable Extensive Cracking,
totally split apart
TABLE 7
Material Volume Hardness Physical
Chg. Chg. Chg.
100% Nylon + .75% + 1 pt. None 909 Nylon/10% Halar + .528 + 1 pt. None 50S Nylon/50% Halar + 2.1% - 8 pts. None
10% Nylon Halar + .98% - 2 pts. None 100% Halar +1.18% - 3 pta. None
Claims (15)
- CLAIMS 1. A method of encapsulating an elongate metal line, suitable for positioning in a subsurface well, and comprising extruding a first-selected polymer circumferentially about a first section of the line having a preselected length; extruding a second-selected polymer circumferentially about a second section of the line having a predetermined length; and extruding a composite polymer circumferentially about an intermediate section of the line between the first and second sections, the composition of the composite polymer varying along the intermediate length of the line from a high first-selected polymer/low second-selected polymer composition to a low first-selected polymer/high second-selected polymer composition, such that a continuous extruded encapsulant is formed interconnecting the first- and second-selected polymers, and substantially no part of the extruded mixture having substantially equal proportions of the first- and second-selected polymers.
- 2. A method according to claim 1, wherein the first-selected polymer is a nylon-based polymer, and the second-selected polymer is a fluoropolymer-based polymer.
- 3. A method according to claim 1 or claim 2, wherein the composition of the composite polymer varies uniformly with the length of the intermediate section.
- 4. A method according to any of claims 1 to 3, wherein the metal line is a tubular line for transmitting fluid and/or fluid pressure signals to any portion of the well.
- 5. A method according to any of claims 1 to 4r wherein the metal line is preheated prior to extruding the composite polymer on the intermediate section.
- 6. A method according to any of claims 1 to 5r wherein the extruded composite polymer is air or water cooled.
- 7. A method according to any of claims 1 to 6r wherein the temperature of the composite polymer upon extrusion of the intermediate section is above the melting temperature of the first-selected polymer, but below the decomposition temperature of the first-selected polymer.
- 8. An encapsulated metal line, suitable for positioning in a hostile subsurface environment, and comprising a first-selected polymer encapsulant circumferentially positioned about a first length of the line; a second-selected polymer encapsulant circumferentially postioned about a second length of the line; and a composite polymer circumferentially positioned about an intermediate section of the line between the first and second lengths, the composition of the composite polymer varying along the intermediate length from a high first-selected polymer/low second-selected polymer composition to a low first-selected polymer/high second-selected polymer composition, such that a continuous encapsulant is formed interconnecting the first- and second-selected polymer encapsulants, and substantially no part of the extruded mixture having substantially equal proportions of the first- and second-selected polymer.
- 9. A metal line according to claim 8, wherein the first-selected polymer is a nylon-based polymer, and the second-selected polymer is a fluoropolymer-based polymer.
- 10. A metal line according to claim 8 or claim 9r wherein the composition of the composite polymer varies uniformly with the length of the intermediate section.
- 11. A metal line according to any of claims 8 to 10, wherein the metal line is of tubular configuration for transmitting fluid and/or fluid pressure signals through the hostile environment.
- 12. An encapsulated metal line for use in a subterranean well having a hostile environment in its lower portions, and comprising a first-selected polymer encapsulant circumferentially surrounding first portions of the metal line to be disposed in the upper portion of the well, the first-selected polymer encapsulant comprising a nylon-based polymer; a second-selected polymer encapsulant circumferentially surrounding second portions of the metal line to be disposed in the lower hostile environment portion of the well, the second-selected polymer being fluoropolymer-based polymer; a composite circumferentially surrounding the portions of the metal line between the first and second portions of the metal line and comprising an extruded mixture of the first- and second-selected polymers, the extruded mixture having a vertically changing composition from a substantial majority of the first-selected polymer and a minority of the second-selected polymer in its upper portions to a substantial majority of the second-selected polymer and a minority of the first-selected polymer in it lowermost portions; and substantially no part of the extruded mixture having substantially equal proportions of the first-selected polymer and the second-selected polymer.
- 13. An encapsulated line according to claim 12, wherein the extruded mixture has a vertically changing composition from substantially 90% of the first-selected polymer and substantially 10% of the second-selected polymer in its upper portions to substantially 90% of the second-selected polymer r and substantially 10% of the first-selected polymer in it lowermost portion.
- 14. An encapsulated line according to claim 12 or claim 13, wherein the metal line is of tubular configuration for transmitting fluid and or fluid pressure signals through the hostile environment.
- 15. An encapsulated metal line, substantially as described.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US28306888A | 1988-12-12 | 1988-12-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
GB8928062D0 GB8928062D0 (en) | 1990-02-14 |
GB2226520A true GB2226520A (en) | 1990-07-04 |
Family
ID=23084356
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8928062A Withdrawn GB2226520A (en) | 1988-12-12 | 1989-12-12 | Extruding a continuous polymeric encapsulant of varying composition over a metal line |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB2226520A (en) |
NL (1) | NL8903052A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998037302A1 (en) * | 1997-02-21 | 1998-08-27 | Downhole Products Plc | Casing centraliser |
WO1999025949A3 (en) * | 1997-11-15 | 1999-07-15 | Brunel Oilfield Serv Uk Ltd | Improvements in or relating to downhole tools |
USD665824S1 (en) | 2011-10-28 | 2012-08-21 | Top-Co Cementing Products Inc. | Casing centralizer |
USD665825S1 (en) | 2011-10-28 | 2012-08-21 | Top-Co Cementing Products Inc. | Casing centralizer |
USD674817S1 (en) | 2011-10-28 | 2013-01-22 | Top-Co Cementing Products Inc. | Casing centralizer |
USD674818S1 (en) | 2011-10-28 | 2013-01-22 | Top-Co Cementing Products Inc. | Casing centralizer |
USD849800S1 (en) | 2012-04-04 | 2019-05-28 | Summit Energy Services, Inc. | Casing centralizer having spiral blades |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB888166A (en) * | 1958-09-05 | 1962-01-24 | Comp Generale Electricite | Process for the manufacture of electric cables having coloured sheathing |
GB938944A (en) * | 1960-09-29 | 1963-10-09 | Delore Sa Geoffroy | Method and apparatus for applying coverings to wires and like elongated members by extrusion |
GB1320213A (en) * | 1969-10-13 | 1973-06-13 | Sherwood Medical Ind Inc | Manufacturing tubing |
GB1345540A (en) * | 1970-04-28 | 1974-01-30 | Dynamit Nobel Ag | Thermoplastic extrudates of mottled appearance |
-
1989
- 1989-12-12 GB GB8928062A patent/GB2226520A/en not_active Withdrawn
- 1989-12-12 NL NL8903052A patent/NL8903052A/en not_active Application Discontinuation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB888166A (en) * | 1958-09-05 | 1962-01-24 | Comp Generale Electricite | Process for the manufacture of electric cables having coloured sheathing |
GB938944A (en) * | 1960-09-29 | 1963-10-09 | Delore Sa Geoffroy | Method and apparatus for applying coverings to wires and like elongated members by extrusion |
GB1320213A (en) * | 1969-10-13 | 1973-06-13 | Sherwood Medical Ind Inc | Manufacturing tubing |
GB1345540A (en) * | 1970-04-28 | 1974-01-30 | Dynamit Nobel Ag | Thermoplastic extrudates of mottled appearance |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6435275B1 (en) | 1997-02-21 | 2002-08-20 | Downhole Products Plc | Casing centralizer |
GB2329209A (en) * | 1997-02-21 | 1999-03-17 | Downhole Products Plc | Casing centraliser |
WO1998037302A1 (en) * | 1997-02-21 | 1998-08-27 | Downhole Products Plc | Casing centraliser |
GB2329209B (en) * | 1997-02-21 | 2000-05-24 | Downhole Products Plc | Casing centraliser assembly |
GB2347953A (en) * | 1997-11-15 | 2000-09-20 | Brunel Oilfield Services | Improvements in or relating to downhole tools |
GB2347953B (en) * | 1997-11-15 | 2002-07-24 | Brunel Oilfield Services | Casing centraliser |
US6666267B1 (en) | 1997-11-15 | 2003-12-23 | Brunel Oilfield Services (Uk) Limited | Downhole tools |
WO1999025949A3 (en) * | 1997-11-15 | 1999-07-15 | Brunel Oilfield Serv Uk Ltd | Improvements in or relating to downhole tools |
USD674817S1 (en) | 2011-10-28 | 2013-01-22 | Top-Co Cementing Products Inc. | Casing centralizer |
USD665825S1 (en) | 2011-10-28 | 2012-08-21 | Top-Co Cementing Products Inc. | Casing centralizer |
USD665824S1 (en) | 2011-10-28 | 2012-08-21 | Top-Co Cementing Products Inc. | Casing centralizer |
USD674818S1 (en) | 2011-10-28 | 2013-01-22 | Top-Co Cementing Products Inc. | Casing centralizer |
USD849800S1 (en) | 2012-04-04 | 2019-05-28 | Summit Energy Services, Inc. | Casing centralizer having spiral blades |
USD983231S1 (en) | 2012-04-04 | 2023-04-11 | Summit Casing Services, Llc | Casing centralizer having spiral blades |
Also Published As
Publication number | Publication date |
---|---|
NL8903052A (en) | 1990-07-02 |
GB8928062D0 (en) | 1990-02-14 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |