CA2433586C

CA2433586C - Thinners for invert emulsions

Info

Publication number: CA2433586C
Application number: CA2433586A
Authority: CA
Inventors: Heinz Muller; Jeffrey P. Kirsner; Kimberly Burrows
Original assignee: Cognis Deutschland GmbH and Co KG; Halliburton Energy Services Inc
Current assignee: BASF Personal Care and Nutrition GmbH; Halliburton Energy Services Inc
Priority date: 2000-12-29
Filing date: 2000-12-29
Publication date: 2010-03-30
Anticipated expiration: 2020-12-29
Also published as: EP1356010A1; AU2001226085B2; CY1111234T1; BR0017399B1; DE60044619D1; NO20032921D0; US7435706B2; CA2433586A1; US20060073987A1; BR0017399A; DK1356010T3; MXPA03005917A; NO20032921L; AR052749A1; ATE472583T1; ES2345922T3; WO2002053675A1; EP1356010B1

Abstract

A method of reducing the viscosity of oil-based drilling fluids and well service fluids at low temperatures and a thinner compound for use in such drilling fluids and well service fluids is disclosed. The method comprises adding to said drilling fluids or well service fluids a thinner having the formula: R-(C2H4O)n(C3H6O)m(C4H8O)k-H where R is a saturated or unsaturated, linear or branched alkyl radical having about 8 to about 24 carbon atoms, n is a number ranging from about 1 to about 10, m is a number ranging from about 0 to about 10, and k is a number ranging from about 0 to about 10.

Description

THINNERS FOR INVERT EMULSIONS

Background of the Invention 1. Field of the Invention This invention is generally related to methods and compositions for drilling and servicing wellbores in hydrocarbon bearing subterranean formations. Particularly, this invention is related to oil-based drilling fluid systems comprising water-in-oil invert emulsions, and to thinners that enhance or enable use of such fluids, at temperatures at or below about 50 degrees Fahrenheit (about 10 degrees Centigrade).

2. Description of Relevant Art A drilling fluid, or "mud" which a drilling fluid is also often called, is a specially designed fluid that is circulated in a wellbore as the wellbore is being drilled to facilitate the drilling operation. The various functions of a drilling fluid include removing drill cuttings from the wellbore, cooling and lubricating the drill bit, aiding in support of the drill pipe and drill bit, and providing a hydrostatic head to maintain the integrity of the wellbore walls and prevent well blowouts.
Specific drilling fluid systems are selected to optimize a drilling operation in accordance with the characteristics of a particular geological formation.
A drilling fluid typically comprises water and/or oil or synthetic oil or other synthetic material or synthetic fluid ("synthetic") as a base fluid, with solids in suspension. A non-aqueous based drilling fluid typically contains oil or synthetic as a continuous phase and may also contain water dispersed in the continuous phase by emulsification so that there is no distinct layer of water in the fluid. Such dispersed water in oil is generally referred to as an invert emulsion or water-in-oil emulsion.
A number of additives may be included in such oil based drilling fluids and invert emulsions to enhance certain properties of the fluid. Such additives may include, for example, emulsifiers, weighting agents, fluid-loss additives or fluid-loss control agents, viscosifiers or viscosity control agents, and alkali.
Further general discussion and description of oil-based drilling fluids is provided in P.A. Boyd, et al., New Base Oil Used In Low Toxicity Oil Muds, Journal of Petroleum Technology, pages 137-142 (1985).
An essential criterion for assessing the utility of a fluid as a drilling fluid or as a well service fluid is the fluid's rheological parameters, particularly under drilling and welibore conditions. For use as a drilling fluid, or as a fluid for servicing a well, the fluid must be capable of maintaining certain viscosities suitable for drilling and circulation in the wellbore. Preferably, a drilling fluid will be sufficiently viscous to be capable of supporting and carrying to the surface of the well drill cuttings without being so viscous as to interfere with the drilling operation. Moreover, a drilling fluid must be sufficiently viscous to be able to suspend barite and other weighting agents. However, increased viscosity can result in problematic sticking of the drill string, and increased circulating pressures can contribute to lost circulation problems.
Thinners may be added to the drilling fluid or drilling mud systems before and in the course of drilling. Anionic surfactants particularly from the group of the fatty alcohol sulfates, the fatty alcohol ether sulfates and the alkylbenzenesulfonates are examples of such thinners known in the prior art.
Although such compounds have been shown to effect thinning of drilling fluids, problems with such prior art thinners may occur when using the drilling muds at low temperatures (temperatures at or below about 50 F (10 C)).
At such low temperatures, despite the use of known prior art thinners, oil based drilling fluids typically have high or increased viscosity, which may render the fluids unusable for drilling. After pumping into the wellbore, drilling fluids may undergo heating from the formation, depending on the depth of thewellbore and the temperature of the formation. For example, heating in the range of about 1500 to about 250 F (about 66 to about 121 C) is not uncommon and subterranean temperatures as high as about 350 F (about 178 C), particularly in very deep wellbores, are known. The Arctic region, for example, is known to have very low surface temperatures but very high subterranean temperatures. Even more problematic are deepwater wells (i. e., typically wells below at least about 1500 feet), which subject drilling fluids to chilling from cold waters surrounding the riser as the fluid returns to the surface from the high temperature subterranean formation. Such chilling of oil based drilling fluids typically increases their viscosity while such subterranean heating of oil based drilling fluids typically reduces their viscosity.
Preferably, thinners which reduce the viscosity of drilling fluids at low temperatures will not affect the viscosity of the fluids at high temperatures.
That is, in many casqs, a thinner is desired that is capable of "selectively"
influencing the rheology or particularly reducing the viscosity of oil-based drilling fluids only at lower temperatures, such as may be encountered at the ground surface of the wellbore, or in the riser surrounded by waters above a deepwater offshore well, for example.
Thinners and other additives to drilling fluids, as well as drilling fluids employed in onshore and offshore wells, must commonly meet stringent environmental regulations related to biodegradability and toxicity. Further, drilling fluids and additives to drilling fluids must be able to withstand subterranean conditions that the fluids will typically encounter in a wellbore, such as high temperatures, high pressures, and pH changes.
A need exists for improved rheology-modifying or viscosity reducing additives to oil-based drilling fluids, and particularly to drilling fluids comprising invert (water-in-oil) emulsions, which are expected to be used in or to encounter low temperatures in drilling operations. As used herein, unless indicated otherwise, "low temperatures" shall be understood to mean temperatures at or below about 50 F (about 10 C).

Summary of the Invention According to the method of the present invention, a compound is added to a water-in-oil or invert emulsion drilling fluid or well service fluid which reduces the viscosity of the drilling fluid or well service fluid at low temperatures or which enables or enhances the ability of the drilling fluid or well service fluid to maintain its viscosity at low temperatures. The compound, which may be generally called a "thinner," continues to have this effect on a drilling fluid or well service fluid in drilling or servicing wellbores in subterranean formations, particularly hydrocarbon bearing subterranean formations. Further, this compound does not significantly affect the viscosity of the emulsion at high temperatures.

The compound has the following formula:' R-(C2H40)n(C3H60)m(C4H84)k-H

where R is a saturated or unsaturated, linear or branched alkyl radical having about 8 to about 24 carbon atoms, n is a number ranging from about I to about 10, m is a number ranging from about 0 to about 10, and k is a number ranging from about 0 to about 10.
The invention also comprises the composition of a water-in-oil or invert emulsion drilling fluid or well service fluid containing this thinner compound.
Brief Description of the Drawings Figure 1 is a graph comparing yield point of mud systems with and without thinners of the invention tested as reported in Table 2 at different temperatures.
Figure 2 is a graph comparing yield point of mud systems with and without thinners of the invention tested as reported in Table 3 at different temperatures.
Figure 3 is a graph comparing yield point of mud systems with and without thinners of the invention tested as reported in Table 4 at different temperatures.
Figure 4 is a graph comparing yield point of mud systems with and without thinners of the invention tested as reported in Table 5 at different temperatures.
Figure 5 is a graph comparing yield point of mud systems with and without thinners of the invention tested as reported in Table 6 at different temperatures.
Figure 6 is a graph comparing yield point of mud systems with and without thinners of the invention tested as reported in Table 7 at different temperatures.
Figure 7 is a graph comparing yield point of mud systems with and without thinners of the invention tested as reported in Table 8 at different temperatures.

Figure 8 is a graph comparing yield point of mud systems vvith and without thinners of the invention, tested as reported in Table 9 at different temperatures.

Detailed Description of Preferred Embodiments The present invention provides a method of influencing the rheology, and particularly reducing the viscosity, of drilling fluids or well service fluids comprising invert (water-in-oil) emulsions. The method is particularly applicable to fluids for use in wellbores penetrating hydrocarbon bearing subterranean formations and has particular advantage in applications where the fluids are subjected to low temperatures, as in drilling or in servicing deepwater offshore wells. Such drilling fluids and well service fluids typically comprise a continuous oil phase, water dispersed in the oil phase, solids insoluble in the drilling fluid or well service fluid suspended in the fluid, and various additives. As the term is used herein, "invert emulsion" or "oil-in-water emulsion" is understood to mean the liquid portion of the drilling fluid comprising an emulsion (excluding solids). The term "invert emulsion drilling fluid" means the total sum of what is circulated as a drilling fluid.
In the method of this invention, a composition or compound having the following formula (I) is added to the invert emulsion or oil-based drilling fluid (or weil service fluid) to reduce the viscosity of the fluid or to enhance the ability of the fluid to maintain its viscosity or to resist increasing viscosity at low temperatures. The compound may be added to the fluid during initial preparation of the fluid or later as the fluid is being used for drilling or well service purposes in the formation. The quantity added is an effective amount to maintain or effect the desired viscosity of the drilling fluid. For purposes of this invention, an "effective amount" of thinner of formula (I) is preferably from about 0.5 to about 15 pounds per barrel of drilling fluid or mud. A more preferred amount of thinner ranges from about 1 to about 5 pounds per barrel o,f drilling fluid and a most preferred amount is about 1.5 to about 3 pounds thinner per barrel of drilling fluid.
Formula (I) is:
(I) R-(C2H40)n(C3H60)m(C4H80)k-H

where R is a saturated or unsaturated, linear or branched, alkyl radical having about 8 to about 24 carbon atoms, n is a number ranging from, about 1 to about 10, m is a number ranging from about 0 to about 10, and k is a number ranging from about 0 to about 10. Preferably, R has about 8 to about 18 carbon atoms; more preferably, R has about 12 to about 18 carbon atoms; and most preferably, R has about 12 to about 14 carbon atoms. Also, most preferably, R
is saturated and linear.
The compositions or compounds of formula (1) may be prepared by customary techniques of alkoxylation, such as alkoxylating the corresponding fatty alcohols with ethylene oxide and/or propylene oxide or butylene oxide under pressure and in the presence of acidic or alkaline catalysts as is known in the art. Such alkoxylation may take place blockwise, i.e., the fatty alcohol may be reacted first with ethylene oxide, propylene oxide or butylene oxide and subsequently, if desired, with one or more of the other alkylene oxides.
Alternatively, such alkoxylation may be conducted randomly, in which any desired mixture of ethylene oxide, propylene oxide and/or butylene oxide is reacted with the fatty alcohol.
In formula (I), the subscripts n and m respectively represent the number of ethylene oxide (EO) and propylene oxide (PO) molecules or groups in one molecule of the alkoxylated fatty alcohol. The subscript k indicates the number of butylene oxide (BO) molecules or groups. The subscripts n, m, and k need not be integers, since they indicate in each case statistical averages of the alkoxylation. Included without limitation are those compounds of the formula (I) whose ethoxy, propoxy, and/or butoxy group distribution is very narrow, such as for example, "narrow range ethoxylates" also called "NREs" by those skilled in the art.
To accomplish the purposes of this invention, the compound of formula (I) must contain at least one ethoxy group. Preferably, the compound of formula I will also contain at least one propoxy group (C3H6O-) or butoxy group (C4H80-). Mixed alkoxides containing all three alkoxide groups-ethylene oxide, propylene oxide, and butylene oxide-are possible for the invention but are not preferred.

Preferably, for use according to this invention, the compound of formula (I) will have a value for m ranging from about 1 to about 10 with k zero or a value for k ranging from about 1 to about 10 with m zero. Most preferably, m will be about 1 to about 10 and k will be zero.
Other preferred compounds for use in the invention having the formula (I) above will have n ranging from about 1 to about 6, m ranging from about 1 to about 6, and k zero. Still other preferred compounds for use in the invention having the formula (I) above will have n ranging from about 2 to about 5, and m being about 3 or about 4 with k zero. It is particularly advantageous to establish the distribution of ethylene oxide and propylene oxide groups in the compounds of formula (I) in an ethylene oxide to propylene oxide ratio of about 1:1 to about 2:1, or even more preferably, about 2:1.5.
Additional preferred compounds for use in the invention having formula (I) above will have alkyl radicals containing about 12 to about 18 carbon atoms, or more preferably about 12 to about 14 carbon atoms, with subscripts n and m each having values of about 4 or about 5.
Used as thinners according to the method of the invention, the compounds of formula (I) reduce the viscosity or lower the yield point of the drilling fluid to which they are added. These thinners are particularly effective at low temperatures, i.e., temperatures at or below about 50 F (about 10 C) and most particularly effective at temperatures at or below about 40 F (about 4 C). The lower limit of effectiveness for these thinners is about 14 F (about -10 C). The thinners do not significantly influence or affect the rheology of drilling fluids at high temperatures, particularly temperatures ranging from about 100 to about 250 F or more.
The compounds of formula (I) are biodegradable and are of little or no toxicity. They are expected to be capable of meeting increasingly stringent environmental regulations affecting the oil and gas industry worldwide.
Example drilling fluids comprising invert (water-in-oil) emulsions of particular use in the method of the invention generally have an oil phase comprising diesel oil, paraffin oil and/or mineral oil, or a synthetic oil.
Alternatively, other carrier fluids may be used such as carboxylic esters, alcohols, ethers, internal olefins, alphaolefins (10 and/or AO), and polyalphaolefins (PAO), which may be branched or unbranched but are preferably linear and preferablyecologically acceptable (non-polluting oils).
Preferably, the oils or carrier fluids used for the oil phase of the drilling fluid will be comprised of compounds which are flowable and pumpable at temperatures above about 32 F (about 0 C) or at least as low as about 40 F
(about 5 C) as well as at higher temperatures. For example, compounds selected from one or more of the following groups or classes below are believed particularly suitable to comprise the oil phase of drilling fluids used in the present invention:

(a) most preferably, carboxylic esters of the formula:
R'-COO-R" (II) where R 'is a saturated or unsaturated, linear or branched, alkyl radical having about 1 to about 23 carbon atoms and R" is an alkyl radical, branched or unbranched, saturated or unsaturated, having about 1 to about 23 carbon atoms;
(b) also preferably, linear or branched olefins having about 8 to about 30 carbon atoms;
(c) water-insoluble symmetric or asymmetric ethers of monohydric alcohols of natural or synthetic origin, said alcohols containing about 1 to about 24 carbon atoms;
(d) water-insoluble alcohols of the formula:
R'll-OH (III) where R"' is a saturated, unsaturated, linear or branched alkyl radical having about 8 to about 24 carbon atoms; and (e) carbonic diesters.

Such suitable oils are taught further, for example, in: European Patent Applications 0 374 671, 0 374,672, 0 382 070, and 0 386 638 of Cognis;
European Laid-Open Specification 0 765 368 of Cognis (linear olefins);
European Application 0 472 557 (water insoluble symmetric or asymmetric ethers of monohydric alcohols of natural or synthetic origin containing about I
to about 24 carbon atoms); European Application 0 532 570 (carbonic diesters). Carboxylic esters of formula (II) above are preferred for the oil phase of drilling fluids used in this invention and particularly preferred are the esters described in European Laid-Open Specification EP 0 374 672 and EP 0 386 636.
In a preferred embodiment of this invention, compounds of formula (I) are added to drilling fluids comprising invert emulsions having an oil phase comprising esters of formula (II) where the radical R' in formula (ti) is an alkyl radical having about 5 to about 21 carbon atoms (or more preferably about 5 to about 17 carbon atoms or most preferably about 11 to about 17 carbon atoms).
Particularly suitable alcohols for making such esters are branched or unbranched alcohols with about 1 to about 8 carbon atoms, for example, methanol, isopropanol, isobutanol, and 2-ethylhexanol. Alcohols having about 12 to about 18 carbon atoms may alternatively be preferred for making other esters suitable for the invention.
For example, additional preferred esters for the oil phase of drilling fluids used in the invention include, without limitation: saturated C12-C14 fatty acid esters and unsaturated C16-C18 fatty acids (with isopropyl-, isobutyl- or 2-ethylhexanol as the alcohol component); 2-ethylhexyl octanoate; acetic acid esters, especially acetates of C8-C18 fatty alcohols; branched carboxylic esters disclosed in WO 99/33932 of Chevron or EP 0 642 561 of E~xxon; alpha olefin mixtures disclosed in EP 0 765 368 Al of Cognis and Halliburton; and blends of these various esters.
The oil phase of the emulsions of the drilling fluids used in the invention is preferably comprised of at least about 50 % by volume of one or more preferred compounds (a) - (e) above. More preferably, such preferred compounds comprise about 60% to about 80% by volume of said oil phase, and most preferably, such preferred compounds comprise about 100% of the oil phase.
Water is preferably present in the liquid phase of the drilling fluids used in the invention, and preferably in amounts not less than about 0.5% by volume (excluding solids in the liquid phase). In a preferred embodiment of this invention, thinners of formula (I) are added to drilling fluids comprising invert emulsions containing about 15 to about 35% by volume water and more preferably 20% by volume water and about 80% by volume oil phase. To compensate for the osmotic gradient between the drilling mud and the formation or connate water, water in drilling fluids used in the present invention typically includes fractions of electrolytes, such as calcium salts and/or sodium salts. CaCI2 in particular is frequently used, although other salts from the group of alkali metals and/or alkaline earth metals are also suitable, with potassium acetates and formates being common examples.
Preferred drilling fluids used in this invention have the following rheology: plastic viscosity (PV) in the range of about 10 to about 60 cP, and preferably in the range of about 15 to about 40 cP, and yield point (YP) in the range of about 5 to about 40 Ib/100 ft2, and preferably in the range of about to about 25 Ib/100 ft2 , at about 122 F (about 50 C). At lower temperatures, i.e., at or below about 40 F (about 4 C), the YP should not exceed about 75 Ib/100 ft2 , and should preferably be in the range of about 10 to about 65 Ib/100 ft2, 1'5 more preferably about 15 to about 45 Ib/100 ft2 , and most preferably less than about 35 Ib/100 ft2. A preferred practicable lower limit for YP for drilling fluids used in this invention is about 5 Ib/100 ft2.
Methods for determining these parameters of PV and YP are well known to those skilled in the art. An example reference is "Manual of Drilling Fluids Technology", particularly the chapter on Mud Testing, available from Baroid Drilling Fluids, Inc., in Houston, Texas (USA), incorporated herein by reference.
The solids content (not including low gravity solids), or the amount of weighting agents, in drilling fluids used in this invention is preferably about 0 to about 500 Ib/bbl, and most preferably about 150 to about 350 Ib/bbl. The mud weight, i.e., the density of the drilling fluids, is preferably in the range of about 8 to about 18 lb/gal. and more preferably about 9 to about 15 lb/gal. Such solids, or weighting agents, which serve to increase the density of the drilling fluids, may be any solids known to those skilled in the art as useful for such purpose, but will preferably be inert or environmentally friendly.
Drilling fluids used in this invention may optionally also contain other additives known to those skilled in the art, such as fluid-loss control additives and emulsifiers. Alkali may also be used, preferably lime (calcium hydroxide or calcium oxide), to bind or react with acidic gases (such as CO2 and H2S) encountered during drilling in the formation. Such alkali, or an alkali reserve, is known to prevent hydrolysis by acidic gases of generally acid-labile esters of the drilling fluid. Preferred quantities of free lime in the driliing fluids range from about 1 to about 10 lbs/bbl, and more preferably about 1 to about 4 lbs/bbi, although lower ranges such as less than about 2 lbs/bbl are preferred for certain esters that tend to hydrolyze in the presence of alkaline compounds as will be known to those skilled in the art. Other suitable agents as an alternative to lime may also be used to adjust and/or stabilize invert emulsions of the drilling fluids with respect to acids. An example of such alternative agents is a protonated amine, as described in U.S Patent No. 5,977,031.
Further optional additives that may be present in the drilling fluids used in this invention include electrolytes, such as calcium chloride, organophilic bentonite and organophilic lignite. Glycols and/or glycerol may also be added.
Still further, dispersion aids, corrosion inhibitors and/or defoamers may be used. These and other suitable auxiliaries and additives are used in amounts known to those skilled in the art depending on the conditions of the particular wellbore and subterranean formation.
Although the invention has primarily been described in the context of a method of using compounds of formula (I) as thinners for drilling fluids at low temperatures, the compounds of formula (I) may also be effective as thinners for well service fluids such as spotting fluids or workover fluids at low temperatures.
Further description and use of the invention is shown by the following examples:

Examples To show the effect of the invention, the following experiments were conducted. In each case an invert emulsion drilling mud system of the following general composition was prepared:

Ester bbl 0.496 Water bbl 0.233 Emulsifier lb 6.0 Organophilic bentonite lb 1.0 Organophilic lignite lb 5.0 Alkali reserve (lime) lb 1.5 CaCI2 x 2 H20 lb 27.2 Barite lb 314.0 Dispersing auxiliary lb 0.5 Thinner lb/bbl 2.0 The oil phase (A) used was a 2-ethyihexyl octanoate as disclosed in EP 0 386 636. The emulsifier used was the product EZ MUL NTE (Baroid Drilling Fluids Inc., Houston, Texas). The oil/water ratio was 70/30 in each case. Measurements were carried out on a system without thinner (C1), and with a C1ti14 fatty alcohol sulfate + 2 E0, sodium salt (C2), with a C12 ether sulfate, sodium salt (C3) and with an oleic acid sulfonate disodium salt (C4), respectively, as prior art thinners, and comparison was made with these thinners and with compounds of formula (I) in accordance with the invention.
The formula (I) compounds used for this purpose were as follows:

El C12/C14 fatty alcohol containing 2 EO and 4 PO
E2 C12/C14 fatty alcohol containing 5 EO and 4 PO
E3 C12/C18 fatty alcohol containing 5 EO and 4 PO
E4 C12/C14 fatty alcohol containing 6 EO and 4 PO

The invert muds were prepared in a conventional manner and subsequently, at 40 F and 122 F, the rheological characteristics of plastic viscosity (PV) and yield point (YP) and the gel strength after 10 seconds and minutes using a Fann SR12 rheometer (from Fann) were determined.

Measurements E5, E6 and E7 were carried out using the thinners El, E2 and E4, but in contrast to the details above, 45 lb of solids (rev dust, i.e., filter ash) were also added to each of the muds, in order to demonstrate the advantageous action of the compounds of formula (1) used in accordance with the invention in the case of high solids loading of the emulsions. In these cases, the measurements were taken only after 16 hours of aging at 150 F.
The thinner was not added to the muds E5 to E7 until after aging.
The results of the measurements are given in Tables 1 a and 1 b below:

W N m O CY) cM
lll O M O
oD co OD
O
W N 00 ti N

~
W N
O 'It N O
0) (0 N
O
W N aD CY) ..
N CY) CY) N
W
~1- OD Cl) -0) W N
= CY) co W O CO O ~
O I~ N

V 04 N N t0 1- c\l W N I~ O N
~ - CO C'O -N
V O O t[ a-~ O
O (O N l/) 1- (O -LU
O O (O I`
~ ~ - IT
> M N M a0 U CN c~+) (N0 N W N N CD N

4- W O O N (0 v U v c c c O ~ I- N
C:l C
N 0) O

N
M N
~ t-V N O U) U) ~
CO M LO
ca W C) ~O I~ N
CM r O
CNJ
CV) U Ct ~ 1~ N y'' V C-4 N N
a) E =- N c\l a) U rn c O O N
N N N a tn N N
p) E N ~
O
U 'VO 'IT (O N C U_ > LL Q- O a) C.0 n' (L V-' } C) ~ O
r co E
O
N Dõ w O N
E LL
~
O
Q (6 2 F- ~" a (9 b cc The data, especially for the yield point (YP), clearly indicate the advantageous thinning effect of the compounds of formula (I) used in the method and in the emulsions of the invention, especially at low temperatures, in comparison to the prior art. The higher plastic viscosity for E5 to E7 is attributable to the higher proportion of solids in the mud systems.
Further experiments may be seen in Tables 2 to 9. In these cases, the yield point (YP) of the systems tested was investigated at different temperatures and depicted as a graph. This illustrates particularly well the advantageous influence of the compounds of formula (I) on the rheology at low temperatures (40 F, 4 C) without any marked influence at high temperatures (120 F, 50 C). The measurements were carried out using a Fann 35 viscometer (from Fann). The tables also indicate the dial readings at different speeds of rotation per minute (rpm).

In Tables 2 to 9:
PETROFREE LVO is 2-ethylhexyl octanoate (from Cognis, Germany) PETROFREE LEO is linear alpha-olefin (from Cognis, Germany) PETROFREEO is C8-14 fatty acid 2-ethylhexyl ester (from Cognis, Germany) GELTONE 110 is organophilic bentonite (from Baroid, Houston, Texas) Thinner El is Formula I C12/C14 fatty alcohol of the invention containing 2 EO and 4 PO
Thinner E2 is Formula I C12/C14 fatty alcohol of the invention containing 5 EO and 4P0 Table 2 Mud s stem PETROFREELV
Mud weight, lb/gal 14.0 Oil/water ratio 70/30 Contaminant Drill solids E2, Ib/bbi 0 3 5 Temperature, F 40 1120 40 120 40 120 Plastic viscosit , cP 118 40 113 34 107 35 Yield point, Ib/100ft 38 14 25 14 19 13 sec el, Ib/100ft 16 6 10 6 6 6 10 min gel, Ib/100ft22 1 11 13 8 9 8 Fann 35 dial readings 600 rpm 274 94 251 82 233 83 300 rm 156 54 138 48 126 48 200 m 114 40 97 35 88 35 100 m 70 25 56 22 49 22 6r m 17 6 10 7 7 6 3 m 14 5 7 6 5 5 Table 3 Mud system PETROFREE
Mud wei ht, lb/gal 14.0 OiVwater ratio 75/25 Contaminant Excess GELTONE II

E2, Ib/bbl 0 3 Temperature, F 40 120 40 120 Plastic viscosit , cP 180 51 126 50 Yield point, Ib/100ft 230 152 19 125 10 sec el, Ib/100ft 108 64 10 50 10 min gel, Ib/100ft 110 66 13 52 Fann 35 dial readings 600 rm 590 254 271 225 300 rpm 410 203 145 175 200 rm 336 179 103 149 100 rpm 248 146 59 119 6 m 112 79 10 62 3 m 100 70 8 58 Table 4 Mud system PETROFREE LV
Mud weight, lb/gal 16.0 Oil/water ratio 80/20 Contaminant Drill solids E2, !b/bbi 0 3 Temperature, F 40 120 40 120 Plastic viscosit , cP 152 51 142 40 Yield point, fb/100ft 62 27 40 19 sec gel, Ib/100ft 22 10 18 10 10 min ei, Ib/100ft 48 26 22 12 Fann 35 dial readings 600 rm 366 129 324 99 300 m 214 78 182 59 200 m 158 59 130 45 100 m 98 38 78 30 6 m 24 11 16 10 3 m 20 9 12 9 Table 5 Mud system PETROFREE
Mud weight, lb/gal 11.0 Oil/water ratio 70/30 Contaminant Excess GELTONE II

E2, Ib/bbl 0 3 Temperature, F 40 120 40 120 Plastic viscosit , cP 132 31 88 29 Yield point, Ib/100ft 54 53 37 53 10 sec gel, Ib/100ft 33 23 13 26 10 min el, Ib/100ft 38 27 17 30 Fann 35 dial readings 600 m 318 115 213 111 300 rpm 186 84 125 82 200 rpm 139 71 90 70 100 rm 91 54 56 55 6 m 35 25 15 28 3 m 32 21 13 25 Table 6 Mud system PETROFREE
Mud weight, lb/gal 11.0 Oil/water ratio 70/30 Contaminant Drill solids E2, lb/bbl 0 3 Temperature, F 40 120 40 120 Plastic viscosity, cP 110 34 113 34 Yield point, Ib/100ft 90 47 73 44 sec el, Ib/100ft 38 21 27 20 10 min gel, Ib/100ft44 24 30 22 Fann 35 dial readings 600 rm 310 115 299 112 300r m 200 81 186 78 200 rm 157 67 142 64 100 rm 110 50 95 48 6 r m 42 23 31 22 3r m 38 21 27 19 Table 7 Mud system PETROFREE LE
Mud weight, lb/gal 16.4 E2, Ib/bbi 0 3 Temperature, F 40 120 40 120 Plastic viscosit , cP 173 40 107 43 Yield point, Ib/100ft 21 9 18 7 10 sec gel, Ib/100ft 16 8 11 8 10 min el, Ib/100ft 19 11 15 11 Fann 35 dial readings 600 rm 367 89 232 93 300 m 194 49 125 50 200 m 135 35 88 37 100 m 74 22 50 22 6 m 12 5 9 6 3r m 10 4 7 5 Table 8 Mud s stem PETROFREE LE
Mud wei ht, lb/gal 11.6 E2, lb/bbl 0 3 Tem erature, F 40 120 40 120 Plastic viscosity, cP 80 31 56 32 Yield point, lb/100ft 25 18 27 16 sec gel, (b/100ft 12 8 17 9 10 min gel, Ib/100ft 20 11 23 11 Fann 35 dial readings 600 rm 185 80 139 80 300 rm 105 49 83 48 200 rm 77 37 63 37 100 rm 46 24 43 24 6rm 11 7 14 8 3rm 9 6 13 7 Table 9 Mud system PETROFREE LV
Mud weight, lb/gal 14.0 Oil/water ratio 70/30 Contaminant Drill solids E1, lb/bbl 0 3 Temperature, F 40 120 40 120 Plastic viscosity, cP 118 40 113 35 Yield point, lb/100ft 38 14 41 16 10 sec gel, lb/100ft 16 6 16 9 10 min gel, lb/100ft 22 11 20 11 Fann 35 dial readings 600 m 274 94 267 86 300 m 156 54 154 51 200 m 114 40 114 39 100 m 70 25 71 26 6 m 17 6 18 8 3 m 14 5 14 8 FiALtiU"I b The foregoing description of the invention is intended to be a description of preferred embodiments. Various changes in the details of the described composition and method can be made without departing from the intended scope of this invention as defined by the appended claims.

Claims

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

1. A method of influencing the rheology of a drilling fluid or well service fluid comprising an invert emulsion, said method comprising adding to said drilling fluid or well service fluid a compound having the formula:
R-(C2H4O)n(C3H6O)m(C4H8-O)k-H
where R is a saturated or unsaturated, linear or branched alkyl radical having 8 to 24 carbon atoms, n is a number ranging from about 1 to about 10, m is a number ranging from about 1 to about 10, and k is a number ranging from about to about 10, such that the ratio of n to m ranges from about 1:1 to about 2:1, and wherein said compound reduces the viscosity and/or lowers the yield point of the drilling fluid at temperatures at or below about 50°F.

2. The method of claim 1 wherein in said formula, k is zero and the ratio of n to m is about 2:1.5.

3. The method of claim 1 wherein in said formula, n is a number ranging from about 1 to about 6, m is a number ranging from about 1 to about 6, and k is zero.

4. The method of claim 1 wherein said invert emulsion to which said compound has been added comprises a continuous oil phase comprising compounds or compositions flowable and pumpable at temperatures at least as low as about 40 degrees Fahrenheit.

5. The method of claim 4 wherein said oil phase comprises synthetic compounds or compositions selected from the group consisting of: (a) carboxylic esters of the formula: R'-COO-R" where R' is a saturated or unsaturated, linear or branched, alkyl radical having 1 to 23 carbon atoms and R" is an alkyl radical, branched or unbranched, saturated or unsaturated, having 1 to 23 carbon atoms; (b) linear or branched olefins having 8 to 30 carbon atoms; (c) water-insoluble symmetric or asymmetric ethers of monohydric alcohols of natural or synthetic origin, said alcohols containing 1 to 24 carbon atoms; (d) water-insoluble alcohols of the formula: R"'-OH where R"' is a saturated, unsaturated, linear or branched alkyl radical having 8 to 24 carbon atoms; and (e) carbonic diesters.

6. The method of claim 1 wherein said compound is added to said drilling fluid or well service fluid in an amount of about 0.5 to about 1 pound per barrel of said drilling fluid or well service fluid.

7. The method of claim 1 wherein said compound is added to said drilling fluid or well service fluid in quantities ranging from about 0.5 pounds to about 15.0 pounds of said compound per barrel of said drilling fluid or well service fluid.

8. The method of claim 1 wherein said compound does not significantly affect the viscosity of said fluid at temperatures ranging from about 100°F to about 250°F.

9. The method of claim 1 wherein said compound is added to said fluid when said fluid is prepared.

10. The method of claim 1 wherein said compound is added to said fluid while said fluid is circulating in a wellbore.

11. A drilling fluid or well service fluid comprising a continuous synthetic oil phase, water dispersed in said oil phase, solids insoluble in said oil phase, an emulsifier, and a thinner compound having the formula:
R-(C2H4O)n(C3H6O)m(C4H8-O)k-H
where R is a saturated or unsaturated, linear or branched alkyl radical having 8 to 24 carbon atoms, n is a number ranging from about 1 to about 10, m is a number ranging from about 1 to about 10, and k is a number ranging from about 0 to about 10, such that the ratio of n to m ranges from about 1:1 to about 2:1, wherein said oil phase comprises about 50% to about 100% compounds or compositions selected from the group consisting of: (a) carboxylic esters of the formula:
R'-COO-R" where R' is a saturated or unsaturated, linear or branched, alkyl radical having 1 to 23 carbon atoms and R" is an alkyl radical, branched or unbranched, saturated or unsaturated, having 1 to 23 carbon atoms; (b) linear or branched olefins having 8 to 30 carbon atoms; (c) water-insoluble symmetric or asymmetric ethers of monohydric alcohols of natural or synthetic origin, said alcohols containing 1 to 24 carbon atoms; (d) water-insoluble alcohols of the formula: R"'-OH where R"' is a saturated, unsaturated, linear or branched alkyl radical having 8 to 24 carbon atoms; and (e) carbonic diesters; and wherein said fluid has a yield point in the range of about 5 to about 75 lb/100ft2 at temperatures at or below about 40°F, a yield point in the range of about 5 to about 40 lb/100 ft2 at about 122°F, and a plastic viscosity in the range of about 10 to about 60 cP at about 122°F.

12. The drilling fluid or well service fluid of claim 11 having a density of from about 8 to about 18 lbs/gal.

13. The drilling fluid or well service fluid of claim 11 having a yield point of in the range of about 15 to about 45 lb/100 ft at about 40°F.

14. A method of reducing the viscosity of an invert emulsion drilling fluid or well service fluid at temperatures less than about 50°F without significantly affecting the viscosity of the fluid at temperatures in the range of about 100°F
to about 250°F, said method comprising adding to said fluid an effective amount of thinner compound having the formula:

R-(C2H4O)n(C3H6O)m(C4H8O)k-H
where R is a saturated or unsaturated, linear or branched alkyl radical having 8 to 24 carbon atoms, n is a number ranging from about 1 to about 10, m is a number ranging from about 1 to about 10, such that the ratio of n to m ranges from about 1:1 to about 2:1 and k is a number ranging from about 0 to about 10 and the viscosity of the fluid is reduced at temperatures less than about 50°F
without significantly being affected at temperatures in the range of about 100°F to about 250°F; and wherein the oil phase of the invert emulsion is synthetic, comprising about 50% to about 100% compounds or compositions selected from the group consisting of: (a) carboxylic esters of the formula: R'-COO-R" where R' is a saturated or unsaturated, linear or branched, alkyl radical having 1 to 23 carbon atoms and R" is an alkyl radical, branched or unbranched, saturated or unsaturated, having 1 to 23 carbon atoms; (b) linear or branched olefins having 8 to 30 carbon atoms; (c) water-insoluble symmetric or asymmetric ethers of monohydric alcohols of natural or synthetic origin, said alcohols containing 1 to 24 carbon atoms; (d) water-insoluble alcohols of the formula: R"'-OH where R"' is a saturated, unsaturated, linear or branched alkyl radical having 8 to 24 carbon atoms; and (e) carbonic diesters.

15. The method of claim 14 further comprising circulating said fluid in a wellbore and adding said compound to said fluid during said circulation.

16. The method of claim 14 further comprising preparing said fluid and adding said compound to said fluid during said preparation.

17. The method of claim 1 wherein, in said formula, R has 12 to 18 carbon atoms, n and m each have values of about 4 or about 5 and k is zero.

18. The fluid of claim 11 wherein said oil phase comprises esters.

19. The fluid of claim 18 wherein said esters are selected from the group consisting of: saturated C12-C14 fatty acid esters where isopropyl-, isobutyl-or 2-ethylhexanol- is the alcohol component; unsaturated C16-C18 fatty acids where isopropyl-, isobutyl- or 2-ethylhexanol- is the alcohol component; 2-ethylhexyl octanoate; acetic acid esters; acetates of C16-C18 fatty alcohols; branched carboxylic esters; and blends or combinations of one or more thereof.

20. The method of claim 14 wherein in the first formula n and m have a ratio of 2:1.5.

21. The method of claim 14 wherein, after the thinner compound has been added, the fluid has a yield point in the range of about 5 to about 45 lb/100 ft2 at about 40°F.