Solids in borehole fluids
10415331 ยท 2019-09-17
Assignee
Inventors
Cpc classification
B29C33/36
PERFORMING OPERATIONS; TRANSPORTING
B29K2901/00
PERFORMING OPERATIONS; TRANSPORTING
B29L2031/772
PERFORMING OPERATIONS; TRANSPORTING
B29C33/3842
PERFORMING OPERATIONS; TRANSPORTING
B29K2995/0082
PERFORMING OPERATIONS; TRANSPORTING
B29C33/44
PERFORMING OPERATIONS; TRANSPORTING
B29C39/02
PERFORMING OPERATIONS; TRANSPORTING
International classification
B29C33/36
PERFORMING OPERATIONS; TRANSPORTING
E21B21/06
FIXED CONSTRUCTIONS
E21B21/00
FIXED CONSTRUCTIONS
B29C33/44
PERFORMING OPERATIONS; TRANSPORTING
B29C33/38
PERFORMING OPERATIONS; TRANSPORTING
B29C39/02
PERFORMING OPERATIONS; TRANSPORTING
Abstract
Solid polymer objects have size at least 0.5 mm in each of three orthogonal dimensions and shape such that each object has one or more edges, points or corners and/or has a plurality of projections which extend out from a core portion. Such objects may be included in a drilling fluid as a lost circulation additive intended to bridge fractures and mitigate fluid loss. Their angular shape features make it harder for them to slide over fracture faces or each other and helps them to bridge a fracture. A method of making these objects provides a travelling endless belt made of elastomer and defining mould cavities. The mould cavities are filled with a polyerisable liquid composition, which is cured in the mould as the belt advances, and the cured objects are ejected from a mould as the belt bends around a roller.
Claims
1. A method of making solid objects formed of polymeric material, the method comprising: providing at least one mould for the solid objects; introducing a curable liquid composition into the mould; curing the curable liquid composition to a solid state in the mould; and releasing the cured solid objects from the mould; wherein the cured solid objects: have sufficient rigidity to sustain their own shape, have an overall size that allows passage through a jet of a drill bit and that extends at least 0.5 mm in each of three orthogonal dimensions, and have a shape such that each object has one or more edges, points or corners and/or comprises a core portion with a plurality of projections that extend out from the core portion.
2. The method of claim 1, wherein the mould is flexible and the method comprises bending the at least one mould to eject the cured solid objects.
3. The method of claim 2, wherein a plurality of moulds are formed in an endless belt, the method comprising moving the belt through a mould-filling station at which the curable liquid composition is introduced into the mould, through a curing zone and then around a bend at which the cured solid objects are ejected from the moulds in the belt.
4. The method of claim 3, wherein moving the belt around the bend comprises running the belt around a roller to change its direction of motion.
5. The method of claim 1, wherein releasing the cured solid objects from the mould comprises melting or dissolving the mould.
6. The method of claim 1, wherein curing the curable liquid composition comprises a photocuring process in which the composition is irradiated with visible or ultraviolet light to initiate polymerisation.
7. The method of claim 1, further comprising; making the at least one mould by an additive manufacturing process.
8. The method of claim 3, further comprising; making a part of the belt with moulds therein by inkjet printing of a flexible polymer.
9. The method of claim 1, wherein at least some of the cured solid objects have a shape which is at least partially bounded by surfaces which intersect at an edge.
10. The method of claim 9, wherein at least some of the cured solid objects have shapes where an angle between surfaces intersecting at an edge is not more than 150 .
11. The method of claim 1, wherein at least some of the cured solid objects have a shape such that the object has one or more points or corners which include angles which are less than 90 when viewed in two orthogonal directions or which include a solid angle of less than 0.5 steradians.
12. The method of claim 1, wherein at least some of the cured solid objects comprise a core with a plurality of projections that extend out from the core.
13. The method of claim 12, wherein the projections extend out from the core for a distance greater than a distance across the core.
14. The method of claim 1, wherein the cured composition is an organic polymer with a specific gravity in a range from 0.8 to 1.2.
15. The method of claim 1, wherein at least some of the cured solid objects are too large to fit within a sphere of 1mm diameter, but are able to fit within a sphere of 8 mm diameter.
16. The method of claim 1, wherein the cured solid objects are dimensioned such as to be too large to fit inside a sphere of 1.5 mm diameter but small enough to fit inside a sphere with a diameter of 6 mm.
17. The method of claim 1, further comprising; incorporating the objects into a drilling fluid and circulating the drilling fluid down and back up a borehole.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
(3)
(4)
(5)
DETAILED DESCRIPTION
(6)
(7) The circulating drilling fluid provides hydrostatic pressure to prevent the ingress of formation fluids into the wellbore, cools and lubricate the drill string and bit and removes drill cuttings from the bottom of the hole to the surface. Drilling fluid compositions may be water-or oil-based and may include weighting agents, surfactants , polymeric thickeners and other materials.
(8) If there is a fracture in the formation rock penetrated by the borehole, drilling fluid may leak into this fracture and be lost.
(9)
(10) The surfaces 22 meet surfaces 24 at edges 25 and the angle between the two surfaces is approximately 90. The surfaces 24 meet surfaces 26 at edges 27. As shown by
(11) Some surfaces of the objects shown in
(12)
(13)
(14) The objects shown in
(15) If drilling fluid is leaking into a fracture in the formation rock and carries any of the objects of
(16) It will be appreciated that the objects shown in these
(17) For the tetragon of
(18)
(19) As shown by
(20) As the belt 50 travels around the rollers 51, 52, a filling mechanism 58 dispenses a photocurable liquid composition into each cavity. Cavities containing liquid composition are indicated at 59. The belt then passes under lamps 60 which direct ultra-violet or visible light onto the belt, causing photocuring of the composition which polymerises and solidifies. The belt then passes around roller 52 where bending the elastomeric belt 50 causes the mouths of the cavities 56 to open, allowing the moulded objects 62 to be dislodged by a jet of air from nozzle 64 and fall out as shown at 66.
(21) The photocurable liquid composition dispensed into the moulding cavities 56 by the filling mechanism 58 contains one or more materials capable of undergoing polymerisation, together with a photoinitiator such that exposure of the composition to visible or ultra-violet radiation causes the photo initiator to liberate reactive species which react with the polymerisable material and cause polymerisation to begin.
(22) The photo initiator is a compound that it is capable of generating a reactive species effective to initiate polymerisation upon absorption of actinic radiation preferably in the range from 250 to 800 nm. The initiating species which is generated may be a cation or a free radical.
(23) A type I radical photo initiator undergoes a unimolecular bond cleavage (-cleavage) upon irradiation to yield the free radical. A type II radical photo initiator undergoes a bimolecular reaction where the triplet excited state of the photoinitiator interacts with a second molecule, which may be another initiator molecule, to generate a free radical. Typically, the second molecule is a hydrogen donor. Where the second molecule is not another initiator molecule, it may be an amine, alcohol or ether acting as a coinitiator. Preferably, the coinitiator is an amine, most preferably a tertiary amine.
(24) Type I cleavable photo-initators include benzoin ethers, dialkoxy acetophenones, phosphine oxide derivatives, amino ketones, e.g. 2-dimethyl, 2-hydroxyacetophenone, and bis(2,4,6-trimethyl benzoyl) phenyl phosphine oxide.
(25) Type II initiator systems (photoinitiator and coinitiator) include aromatic ketones e.g. camphorquinone, thioxanthone, anthraquinone, 1-phenyl 1,2 propanedione, combined with H donors such as alcohols, or electron donors such as amines.
(26) A cation photo-initiator is preferably a photoacid generator, typically a diazonium or onium salt, e.g. diaryliodonium or triarylsulphonium hexafluorophosphate.
(27) Photo initiator will generally be a small percentage of the polymerisable composition. The percentage of photo initiator in the composition is likely to be a least 0.5% by weight and may extend up to 3% or even 5% by weight of the liquid components of the composition.
(28) The polymerisable composition will generally comprise one or more polymerisable monomers which contain two groups able to participate in the polymerization reaction. Such monomers can extend a growing polymer chain and are likely to provide at least 50% probably at least 80% or 85% of the liquid components of the polymerizable composition. These monomers may be accompanied by a minor proportion of monomers with more than two groups able to participate in the polymerization reaction. Such monomers create branching of polymer chains or cross-linking between polymer chains and may be present as up to 15%, preferably 1 to 10% by weight of the liquid components of the polymerisable composition.
(29) The groups able to participate in the polymerization reaction may be olefinically unsaturated groups. Polymerizable monomers may be esters of an olefinically unsaturated acid and a dihydroxy compound (although such esters may be manufactured using other starting materials such as an acid chloride, of course) The acid moiety is preferably an olefinically unsaturated acid containing 2 to 5 carbon atoms notably acrylic or methacrylic acid.
(30) Some examples of such monomer compounds are: -bisphenol A ethoxylate diacrylates, having the general formula
(31) ##STR00001##
bisphenol A ethoxylate dimethacrylates, having the general formula
(32) ##STR00002##
and poly(ethylene glycol) diacrylates having general formula:
(33) ##STR00003##
(34) In the above three general formulae, m and n are average values and may vary. Generally they will lie in a range up to 15, such as 1 or 1.5 up to 15 but preferably not above 6. We have found that monomers containing ethylene oxide residues improve flexibility of the polymer but reduce its strength.
(35) The composition preferably also includes some monomer with more than two olefinically unsaturated groups, to create branched or cross-linked polymer chains. Such compounds may be acrylate or methacrylate esters of poly hydroxy compounds.
(36) Some examples are as follows:
(37) TABLE-US-00001 Name Formula MW (g/mol) trimethylolpropane triacylate
(38) Monomer compounds with two olefinically unsaturated groups may also be vinyl ethers such as 1,6-hexane diol divinyl ether, poly(ethylene glycol) divinyl ether, bis-(4-vinyl oxy butyl)hexamethylenediurethane, and vinyl ether terminated esters such as bis-(4-vinyl oxy butyl) adipate and bis-(4-vinyl oxy butyl) isophthalate.
(39) Another possibility is that the groups able to participate in the polymerization reaction are epoxide groups. A suitable category of monomer compounds containing epoxide groups are glycidyl ethers of dihydroxy compounds, some specific possibilities being 1,6-hexanediol diglycidyl ether, bisphenol A diglycidyl ether and poly(ethylene glycol) diglycidyl ether.
(40) The polymerisable composition may comprise a mixture of monomers. Notably a mixture of monomers may be used in order to obtain a desired combination of mechanical properties of the polymer lining on the tubing. The monomers will generally provide at least 50 wt % of the composition and preferably from 70 to 99.5 wt % of it.
(41) The polymerisable composition may include one or more solids serving to reinforce it after polymerisation. Such a solid material included to reinforce the composition may be particulate, such as bentonite clay particles, or may be short fibres such as chopped glass fibres. These materials may have an additional effect of enhancing viscosity. Another reason for including a solid would be to raise the specific gravity by adding a solid filler which is denser than the polymer. The polymerisable composition may contain from 0 to 20 wt % of such solids, possibly even up to 30 wt % or above.
(42) The sections 54 of the belt 50 may be made by an additive manufacturing process. An additive manufacturing process may be implemented to construct an object in accordance with a design held in digital form. The process progressively adds material at selected locations within a workspace, so that the added material joins on to material already present. Such a process is termed additive because more material is progressively added in order to arrive at the finished article, in contrast with traditional machining processes which remove material from a workpiece in order to create the desired shape. Several additive processes are known and are sometimes referred to as three-dimensional printing (3D-printing) although that term may also be reserved for one or only some of these additive manufacturing processes.
(43) The term 3D printing may be used for a process which uses a movable printing head to deliver a droplet of a polymerisable liquid composition to each selected location. The composition may for instance be photopolymerisable by ultraviolet or visible light, and the polymerisation is initiated by illuminating the work space with ultra-violet or visible light while the print head delivers droplets of composition to the selected locations. The photopolymerisation joins each droplet onto material which has already been delivered and polymerised. A process of this kind and apparatus for the purpose was described in U.S. Pat. No. 5,287,435 although there have been numerous subsequent developments as for instance disclosed in U.S. Pat. Nos. 6,658,314 and 776,641.
(44) A 3D printing process may be used to print a section 54 of the belt 50 by printing a composition which becomes a rubber-like elastomer as it is printed. This elastomer may be printed using a single composition or by using a combination of an elastomer and a more rigid material, so as to produce a belt 50 which is more rigid, but still bendable. As the elastomer is printed to form the section 54 of belt, a temporary support material is printed at the positions which become mould cavities. When the printing process has been completed this temporary support material is removed, so as to leave empty mould cavities 56.
(45) Machines for 3D printing are available from several manufacturers, including Stratasys, located in Edina, Minnesota and elsewhere. A commercially available 3D-printing machine may for example print objects within a space slightly larger than a 20 cm cube, printing them as layers each of which has a thickness of 16 or 32 microns and a resolution of about 20 points per mm.
(46) Another additive process which provides an alternative way to make sections 54 of the belt 50 is stereolithography in which a volume of polymerisable liquid is selectively polymerised at selected locations by irradiating with a laser as described in U.S. Pat. No. 5,778,567.
(47) The above description has referred to moulds make of an elastomeric material, used to mould objects with a flat surface which corresponds to the surface of liquid in the mould cavity. However, it would be possible to mound shapes without such flat surface, by using moulds made by 3D printing with a material with a melting point in a range from 50 to 100 C. or which is water soluble and which can be melted or dissolved to release the moulded objects.
(48) In another approach for making sections 54 of the belt 52, an additive process such as 3D printing is used to make a preliminary mould for a section 54 of the belt. Such a preliminary mould can take the form of a tray with replicas of the intended objects positioned on the base of the tray and integral with it. Such a mould may be rigid. A section of the belt with mould cavities in it is then made by a casting process in which this preliminary mould is filled with a composition which cures to an elastomer whilst in the mould.
(49) This approach necessitates an additional manufacturing step because the preliminary mould made by 3-D printing is used to make sections 54 of the belt 50, and these sections are subsequently used to make the desired objects such as those shown in
(50) It will be appreciated that the methods described above utilise the ability of additive manufacturing to fabricate desired shapes, such as the complex shapes shown by
(51) It will be appreciated that the example embodiments described above can be modified and varied within the scope of the concepts which they exemplify. Features referred to above or shown in individual embodiments above may be used together in any combination as well as those which have been shown and described specifically. Accordingly, all such modifications are intended to be included within the scope of this disclosure as defined in the following claims.