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Treatment method of bottom-hole formation zone. RU patent 2494245.

Treatment method of bottom-hole formation zone. RU patent 2494245.
IPC classes for russian patent Treatment method of bottom-hole formation zone. RU patent 2494245. (RU 2494245):

E21B43/27 - by use of eroding chemicals, e.g. acids
C09K8/74 - MATERIALS FOR APPLICATIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
Another patents in same IPC classes:
Treatment method of bottom-hole formation zone Treatment method of bottom-hole formation zone / 2494244
In a treatment method of a bottom-hole formation zone, which involves pumping to the formation of acid-oil emulsion of reverse type and acid, as acid-oil emulsion of reverse type there used is emulsion containing the following components, wt %: dispersion medium - hydrocarbon liquid 31-38, emulsifier - reaction products of aliphatic amines of fat acids of hydrated tall oil with hydrochloric acid in terms of amines 0.02-0.08, dispersion medium - synthetic, inhibited hydrochloric acid (10-18%) is the rest.
Method for near well-bore treatment with acid / 2490444
Method for near well-bore treatment with acid involves at the first stage pumping into the well of 10-15% aqueous solution of hydrogen chloride in a volume calculated on the basis of 0.25-0.5 m3 per 1 running metre of penetrated stratum depth; at the second stage - pumping of 10-15% aqueous solution of hydrogen chloride with a retarder of the acid reaction with rock in the volume of 2-5% of acid solution volume in total volume of pumping calculated on the basis of 1-1.5 m3 per 1 running metre of penetrated stratum depth at initial pressure equal to the final pressure value during pumping at the previous stage; overflushing by oil in volume of 5-15 m3 at initial pressure equal to the final pressure value during pumping at the previous stage; soaking during 16-48 hours and input of the well into operation.
Procedure for treatment of bottomhole zone of producer with two wellheads Procedure for treatment of bottomhole zone of producer with two wellheads / 2490443
In procedure for treatment of bottomhole zone with two wellheads in case of failure of an electric-centrifugal pump (ECP) with no apparent deviation in its operating parameters and in case of alkalinity growth for extracted product up to pH>7 the required volume of hydrogen chloride solution is calculated on the basis of a length and diameter of the well filtering part; the required volume of hydrogen chloride solution is selected to treat the whole volume of the strainer; the required volume of flush fluid is calculated for delivery of compounds into a slope wellhead. ECP is shutdown at the vertical wellhead before pumping of hydrogen chloride solution is started. The required volume of hydrogen chloride solution is carried out into tubular annulus from the side of the vertical wellhead. When pumping of hydrogen chloride solution is over extraction from the slope wellhead is increased and ECP is started from the vertical wellhead. ECP is stopped at the vertical wellhead and hydrogen chloride solution is overflushed by the flush fluid into filtering part of the well. After ECP startup in enlarged extraction rate from the slope wellhead samples are taken periodically in order to check pH value, monitor dynamics in changes of fluid supply from the slope wellhead. When pH value id recovered up to the normal value ECP is started into operation from the vertical wellhead and supply from the slope wellhead is returned back to normal operation mode.
Method for well completion / 2490442
In method for well completion including pumping of acid solution into open horizontal hole in the mode of jet impact such impact is attained due to a jet delivery by a jet nozzle at the end of a flexible flush-joint pipe. The nozzle is placed at the borehole bottom. The acid solution is pumped with circulation through the well mouth; while acid solution is circulating the flexible flush-joint pipe is lifted simultaneously from the well with the speed not exceeding speed of the borehole filling by the acid solution. When horizontal hole is filled with the acid solution, the solution is overflushed into the stratum with staged pressure build-up and exposure at each stage. The flexible flush-joint pipe with a nozzle is placed again at the borehole bottom and the operation of borehole filling and overflushing is repeated again. Soaking takes place so that acid solution could react with the rock. The flexible flush-joint pipe is lifted to the interval of inert gas pumping, an inert gas is pumped and a build-up curve is recorded. Cyclic well killing is carried out in the mode of water pumping - soaking - oil draining till complete oil drain; thereafter a submerged pump is run-in and the well is input into operation.
Device for treatment of bottomhole formation zone of a well and method for treatment of bottomhole formation zone of well Device for treatment of bottomhole formation zone of a well and method for treatment of bottomhole formation zone of well / 2487237
Device for treatment of bottomwhole formation zone contains an air chamber with atmosphere pressure and length of 20-50 m connected to the first additional perforated chamber with seal layer, solid heat generating compound A with flame igniter, combustible high-strength compound B and breakable calibrated membrane located inside; the first added perforated chamber by means of a coupling with holes is connected to the second added inlet chamber with combustible high-strength compound C, igniter and breakable calibrated membrane located inside; the second additional perforated chamber by means of a coupling with added air chamber with length of 1.5-3 m connected by means of a coupling and metal adapter with to inlet chamber that is made of elastic plastic material with seal layer, solid acid generating compound D with igniter located inside; in the metal adapter there are drilled holes; compound A generated heat and gas of the following components by wt %: ammonium nitrate 35; sodium bichromate 2; barium nitrate 15; aluminium ASD-1 1.5; iron-aluminium thermite 31; epoxide compound (mixture of ED-20 tar, EDOS plasticiser and AF-2M hardener) 15.5; compound B is made of the following components by wt %: ammonium nitrate 30-40, calcium carbonate 5-10, the above epoxide compound 50-65; inside the added inlet chamber there is a layer of glass sealant and solid gas generating compound E made of the following compounds by wt %: ammonium nitrate 70, sodium bichromate 1, the above epoxide compound 29; compound C is made of the same composition as compound B; compound D is made as thermal-gas-chemical solid fuel with a layer of glass sealant and a layer of epoxide compound on top of it; the above fuel consists of the following components by wt %: ammonium nitrate 12-16, lithium fluoride 1-3, barium nitrate 5-8, aluminium ASD-1 0.7-0.8, iron-aluminium thermite 14-16, hexachlorane 20-30, polytetrafluoroethylene 20-30, the above epoxide compound 5-10. The method for treatment of bottomhole zone (BHZ) includes delivery of the above device by a wireline, combustion of compound D and formation of maximum quantity of chemical agents, holding for the purpose of reaction of acids produced during combustion with BHZ formation, running with installation of the coupling with holes at the level of treated stratum, opening of the chamber with length of 20-50 m, actuation of breakable calibrated membrane in result of layer-by-layer combustion of compounds A and B with implosion treatment of BHZ, removal of impurities from bottomhole stratum; during holding thermal-gas-chemical impact acts on the stratum for 30 minutes ad pressure can be corrected due to availability of holes in the metal adapter at fixed position of the above fuel inside the inlet chamber due to the above layers of sealant and compound with formation of gases heated up to high temperatures at high pressure within treatment range; opening of the chamber with length of 1.5-3 m is carried out by sequential actuation of the igniter, compounds E and C and breakable calibrated membrane located in the second added inlet chamber; after hydraulic shock there's another holding of the process for 30 minutes; when the chamber with length of 20-50 m is opened combustion of compound A takes place with formation of gases heated up to high temperature at high pressure within treatment range.
Stimulation method of formation fluid influx from well Stimulation method of formation fluid influx from well / 2485305
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Method for reagent clay cake removal from well / 2484244
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Method for bottom-hole zone treatment / 2477787
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Acidic aqueous solution containing chelating agent and use thereof Acidic aqueous solution containing chelating agent and use thereof / 2476475
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Treatment method of bottom-hole formation zone Treatment method of bottom-hole formation zone / 2494244
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Preparation method of composition for isolation of lost-circulation zones in well / 2494228
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Methods for using additives containing microgels for controlling fluid loss Methods for using additives containing microgels for controlling fluid loss / 2493190
Mud solution containing an aqueous fluid and an additive to control fluid loss, containing at least one polymer microgel comprising a reaction product prepared by a polymerisation reaction of a polymer or a copolymer and a crosslinking agent, wherein the polymer or copolymer comprises at least one unit of at least one compound from a group of: polybutylene succinate, polybutylene succinate-co-adipate, polyhydroxy-butyrate-valerate, polyhydroxy-butyrate-covalerate, polyester amides, polyethylene terephthalates, sulphonated polyethylene terephthalate, polypropylene, aliphatic aromatic copolyester, chitins, chitosans, proteins, aliphatic polyesters, poly(hydroxyester ethers), poly(hydroxybutyrates), poly(anhydrides), poly(orthoesters), poly(amino acids), poly(phosphazenes), a copolymer thereof, a homopolymer thereof, a tetrapolymer thereof, and any derivative thereof. The method involves: preparing an aqueous compound for well treatment and containing the above additive, introducing the compound into a downhole formation, thereby allowing the additive to flow into a filter cake on the surface inside the downhole formation, allowing the filter cake to degrade, and extracting hydrocarbons from the formations. The method involves preparing the above mud solution, introducing it into the downhole formation, allowing the additive to flow into the filter cake on the surface inside the downhole formation, allowing the filter cake to degrade, and extracting hydrocarbons from the formation. The method involves preparing a filter thickener containing the above aqueous fluid and the additive, placing the thickener into the downhole formation with gravel packed filtration and a portion of the downhole formation. The invention is developed in the secondary claims.
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FIELD: oil and gas industry.

SUBSTANCE: acid treatment method of a bottom-hole formation zone involves pumping to the formation of emulsion and water solution of an acid; at that, first, water solution of acid is pumped, and pumping of water solution of acid and emulsion is performed in a series-and-alternating mode, and emulsion containing the following components, wt %, is used as emulsion: acid 5.0-40.0; emulsifier - anionic or nonionic, or cationic surface-active substance, or their mixture 1.0-10.0; hydrocarbon solvent 5.0-40.0; decomposer - primary or secondary alcohol or their mixture 0.1-5.0; corrosion inhibitor 0.01-0.05 and water is the rest. Emulsion can contain viscosity regulator in the quantity of 0.01-6.0 wt %. Water solution of acid with concentration of 3.0-24.0% is used.

EFFECT: deceleration of a reaction of acid with rock of the formation, enlarging the treatment coverage range as to thickness and depth of the formation using an emulsion, preserving stability, reducing intensity of acid corrosion and having washing effectiveness in relation to asphaltene-resin-wax-bearing deposits.

3 cl, 3 tbl, 29 ex

 

Field : oil producing industry and can be used for acid treatment of bottom-hole formation zone, presented heterogeneous permeability carbonate and terrigenous reservoirs.

A method of processing the well bottom zone in multilayer oil Deposit, including the pumping of oil emulsion all layers, further material, the solvent and the oil component of the oil emulsion, and acid solution, which is injected in oil reservoirs (see Patent of Russian Federation №2092686, MKI 21 43/27, publ. 1997).

This method is not efficient enough because of the complicated processing three different compositions, did not provide a selective penetration of acid in the oil-saturated interlayer and lock emulsion pays. Moreover, loaded emulsion remains in the oil reservoir and worsens its filtration characteristics.

There is a method of acid treatment of bottom-hole formation zone, including, sequential injection emulsion of the following composition, mass%: hydrochloric acid 15-20%concentration - 44.1kHz-51,1, carboxymethylcellulose 1.5 to 2.5,and water - 46,4-54,4 and acid composition that contains, mass%: hydrochloric acid 15-20%concentration, an acid benzojnuju 0,25-0,5 concentration and water - 42,9-62,25 (see RF Patent №2269648, MKI 21 43/27, publ. 2006).

However, a well-known method for technical result aims to increase the depth of penetration of the emulsion into the reservoir by changing the wettability of the breed. There is no effective redistribution of filtration flows, acid emulsion enters the water saturated plot collector and does not cover the reservoir.

Closest to the proposed invention of technical nature and the achieved result is a method treatment of bottomhole formation zone, including injection into the reservoir reverse oil emulsion and water solution acid, where as the inverse emulsion use emulsion, which contains the following components,%: hydrocarbon liquid 26-40, emulsifier -9601 or 9701-0,4-5,0, aqueous solution of inhibited 10%hydrochloric acid or or aqueous solution 1-10%solution of calcium chloride or sodium chloride - the rest (see RF Patent №2255215, MKI 21 43/27, publ. 2005).

However, application of this method is limited, since the time of the breakup emulsions are unregulated depending on the temperature, viscosity and solve technological tasks, the result could be the deterioration of filtration properties of the manifold due to contamination used emulsion, which is not destroyed after the treatment well. Also at the high content of iron in the bottomhole zone the emulsion has a tendency to resinification that leads to sedimentation of oil pays resins, the reaction products of oil with acid in the presence of ions of iron, especially these processes are significant at elevated temperatures.

Purpose the invention is to provide a way of processing of bottom-hole formation zone with high efficiency by slowing the speed of the reaction of acid to the reservoir rock, increase coverage of treatment in thickness and depth of the reservoir, with the use of emulsion, preserving stable up to 120 hours at a temperature up to 60 C, which reduces the intensity of acid corrosion, and has a washing effective against .

This goal is achieved through the creation of a way of processing of bottom-hole formation zone, including injection into the reservoir emulsion and water solution acid, and initially injected water solution of acid, and the pumping of water solution of acid and emulsion is carried out in a series-striped mode and as use emulsion emulsion of the following composition, mass%:

Acid

- 5,0-40,0

or nonionic

or cationic surfactant

or a mixture

- 1,0-10,0

Hydrocarbon solvent

- 5,0-40,0

Primary or secondary alcohol

or a mixture

- 0,1-5,0

Corrosion inhibitor

- 0,01-0,05

Water

- the rest.

In the options for the application of ways emulsion may contain viscosity regulator in the amount of 0.01-6,0 mass%, and acid aqueous solution uses 3.0-24,0%concentration.

As a water solution of acid use aqueous hydrochloric acid or mixtures of hydrochloric and hydrofluoric acids, depending on the reservoir rock.

To the emulsion as acid is used:

- hydrochloric acid GOST 857-95;

- hydrofluoric acid GOST 10484-78;

- acid TU 2121-083-05800142-2001;

- acetic acid GOST 19814-74;

- formic acid GOST 1706-78;

- mix of the two.

Use surfactants or nonionic surfactants or cationic surfactants or their mixtures, such as: TU 6-09-1514-75; - 5K TU 2483-064-0580977-2003; emulsifier cationic bitumen emulsions (Б) TU 0257-007-35475596-98; -04 TU 2458-003-27913102-2003; - monoamine fatty acids of coconut oil, the production of China. - Amdor TU 0257-003-35475596-96.

As a hydrocarbon solvent use:

- diesel fuel (DT) in accordance with GOST 305-82;

- xylene GOST 9410-78;

MIA-prom TU 4852-01127913102-2001;

- toluene GOST 14710-78;

- gasoline on the other 0251-009-057-66801-93;

- the faction of aromatic hydrocarbons (FAA) TU 2414-00352927048-2005;

- mix of the two.

Primary or secondary alcohols enter in structure to regulate the speed of the collapse of the emulsion with the formation of the mobile inorganic and hydrocarbon phases. As primary or secondary alcohols use for example: - methanol GOST 2222-95; - isopropanol TU 6-09-50-2655-94;

- secondary butanol GOST 6006-78;

- TU 6-01-646-84;

- GOST 8313-88; or their mixture.

As a corrosion inhibitor is used:

- Dodicor -2575 - product company «Clariant», USA;

- Prod Ci-300 - a product of the company «Chevron Fillips, USA:

- methenamine GOST 1381-73;

- formaldehyde GOST 1625-89;

fatty ammonium salt.

As a regulator of viscosity can be used:

- ES-3 TU 38-5901268-90;

- biopolymer TU 2458-002-50635131-2003;

- polyacrylamide TU 6-01-1049-92;

Used in the alleged invention emulsion can be prepared as in conditions of industrial production, and immediately prior to use by successive dissolution of the components of the declared quantities.

Give examples of the emulsion.

Example 1 (declared emulsion).

While stirring with a mechanical mixer to 15,0 g hydrochloric acid added to 2.0, , hereinafter referred to as the mixture is injected 40,0 g hydrocarbon solvent mixtures diesel fuel and xylene at a ratio of 85:15, 0,1, methanol, 0.01 g corrosion inhibitor - Dodikor and 42,89 g of water (see table 1, figure 1).

Example 2, 4, 9, 13, 18, 27 prepare as in example 1 without adding primary or secondary alcohols.

Example 3. While stirring with a mechanical agitator to 12.9 g hydrochloric acid added 1.0 g -04, hereinafter referred to as the mixture is injected 12,94, the hydrocarbon solvent - MIA-prom, 4.0 g methanol, 0.01 g corrosion inhibitor - Dodikor, 0.01 g control and viscosity - ES-3 and 69,14 g of water (see table 1 example 3).

Examples 5-8, 10-12, 14-17, 19-26, 28 prepare similarly, changing the kinds of components and their content in the in the declared quantities.

Example 29 (prototype).

In 26,0 g diesel fuel dissolved 0.2 g emulsifier - -9601 at intensive hashing, then in 3 admission impose 7,38 g of hydrochloric acid and stirred for 5 minutes (..1, example 25).

According to the present method of processing of bottom-hole zone of an oil layer of make as follows.

During injection of the first rim aqueous solution of acid into the reservoir is rinsing process equipment and bottomhole formation zone of inorganic salts and iron compounds. Such treatment allows to avoid sedimentation of oil layer of resin, the reaction products of oil with acid in the presence of iron ions. Further pumped emulsion, which is due to the high viscosity of the blocks flushed areas and slows down the speed of reaction to the reservoir rock. The newly injected water solution of acid enters in a zone with low permeability, due to the interaction with the reservoir rock increases the permeability. When further injection of emulsion again, it locks the newly formed high permeability zones, due to the slow reaction with the breed emulsion penetrates deep into formation and, thus, increasing the coverage of the layer effects.

The total volume of emulsion formation treatment is determined proceeding from power of the processed layer, radius processing, porosity and oil saturation factor of the formation according to the following formula: Q=p*R 2 *H*m*KN,

where: Q is the volume of prepared emulsion, m 3 ;

π=3,14;

R is the radius of the processing, m;

H - thickness of the processed layer, m;

m - porosity,%;

KN - factor oil saturation layer. Sequentially, alternating treatment is carried out in 1-5 cycles.

Evaluation of the effectiveness of emulsions checked in the laboratory for determination of viscosity, the dissolution rate of marble, clay and checking the stability of emulsions at a temperature of 60°n Research results are summarized in table 1.

To determine the stability of the emulsion in time in the graduated tube tube pour 100 ml emulsion, placed in an incubator at

temperature of 60 C and note the time for complete separation of organic and acid phases.

Viscosity of emulsions determine the rotational viscometer Fann-35 Measurement is carried out at various speeds of rotation of a spindle. It is permitted to change the viscosity of 15-20% within 6 hours. The results of measurements record indicating the brand of the device, the type of spindle rotation speed and temperature. Table 1 shows the values of the viscosity received on the device Fann-35 at room temperature and speed spindle speed 300 rpm, which corresponds to the speed shift 511 -1 .

The rate of dissolution of carbonates (marble) evaluated according to the following procedure. Cube marble square shape weighed accurate within the second digit linear dimensions calculate the volume of a cube and density. The average density of the used marble 2.5 g/cm 3 . Hanging on a thread cube marble lower in the study composition and at regular intervals (10-30 seconds) are removed, washed with water, dried and weighed make up table with the parameters of the relative time of dissolution of the cube and the absolute values of the mass. The method of least squares found from the angle of inclination of a straight on a linear interval dissolution rate (g/s) in this experiment. The absolute value of the dissolution rate (g/m 2 *s) are as the slope of the straight, calculated at the coordinates (m/S), where m is the mass of the cube at regular intervals, S - size calculated by the equation:

S=6(m/p)2/3.

The rate of dissolution of clay evaluated according to the following procedure. Installation of bentonite clay weight of 2 g mixed with 20 g of the proposed acid composition and incubated for 18 hours. Then the solution was filtered through a filter with a known mass, washed with water and dried at room temperature for up to a constant mass and weighed on the filter. The effectiveness of dissolution is calculated by the formula:

E=100*(M-m)/Mo, where:

M is the mass of the initial clay filter after processing, g;

MoE - original mass of clay,,;

m - mass of the filter,

According to the results, shown in table 1 shows that used in the claimed method emulsion has a high viscosity, is more stable. Reducing the speed of dissolution of the reservoir rock increases the permeability of the composition of deep into formation.

To determine the effectiveness of emulsions in its use for formation treatment determine the rate of corrosion and cleaning efficiency. The results are given in table 2.

Table 2 №№

Number of table 1

Corrosion rate, g/m 2 *h

Cleaning efficiency, %

1 №1 0,29 83 2 №12 0,22 76

3 prototype

HCl - 7,38

0,35 45

-9601 - 0,2

DT - 26,0

Corrosive activity is checked according to the standard technique on metal plates (steel 3) at room temperature.

Plate size 10*15*3 cleaned, washed in warm water, degrease with acetone or alcohol and dried to a constant weight. The plate hung on a nylon thread in the glass so that when you fill a glass with acid butt plate was about 10 mm below the liquid level. Glass fill acid structure and leave on a fixed time. After a specified time a record is removed from the acid, carefully washed in running water and repeatedly rinsed with hot distilled water. The moisture from the surface of the plate is removed by the filter paper plate and dried to a constant weight.

Corrosion rate is calculated by the formula:

V=g/10 -4 *S*t,

where: V - speed of corrosion, g/m 2 *h;

g weight loss plates as a result of corrosion, g;

S - surface of the plate, m2;

t - the duration of the test, the hour.

Definition of the cleaning efficiency of conduct in dynamic terms, what samples (ASPO) weight 2 g placed in the baskets of stainless steel and wire hung up in the layer prepared in advance of the emulsion in a plastic bottle with a volume of 250 ml Mix the contents of the bottles on a magnetic stirrer at a speed of 400 rpm for 2 hours at room temperature. The incident time specimens are removed, rinse water, air-dried and . efficiency is measured as the ratio of the weight loss sample to its original weight percentage.

When comparing the results show that the proposed emulsion has a high detergency efficiency of ARPD is compared with the prototype, has low corrosion activity

To study the effect of the proposed method on the change of filtration in a porous medium using a model of the reservoir, representing paired metal tube length of 50 cm and 3 cm in diameter varying permeability. As source material for creating porous environment of the use of ground quartz sand in pure water and with the addition of % calcium carbonate.. As a saturating fluids using mineralized water with salt content of 19 g/whether degassed oil diluted with kerosene to 4 .. Formation model saturate water in amount of 2 pore volumes, then spend the ousting of its oil, and then pump the water solution of the acid, and then the emulsion and then replacing it with oil. In another version, after pumping oil spend the ousting of its water is then pumped water solution of acid and claimed emulsion, which also displace water. Change filtration resistance is calculated by the formula:

Q = ( K 1 ( in , n ) - K 2 ( in , n ) ) To 1 ( in , n ) * 100 % , where

1,n) and 2 (n) - permeability model for oil and water before and after the injection of a water solution of acid and emulsion, 2 microns .

1. Way of processing of bottom-hole formation zone, including injection into the layer of the emulsion and water solution acid, wherein the first pump the water solution of the acid, and the pumping of water solution of acid and emulsion is carried out in a series-striped mode and in as the use emulsion emulsion of the following composition,% Mas.:

Acid 5,0-40,0

, or nonionic, or

cationic surfactant

or a mixture

1,0-10,0

Hydrocarbon solvent

5,0-40,0

Primary or secondary alcohol

or a mixture

0,1-5,0

Corrosion inhibitor

0,01-0,05

Water Rest

2. The method according to claim 1, characterized in that the emulsion additionally contains viscosity regulator in the amount of 0.01-6,0 mass%.

3. The method according to claim 1, characterized in aqueous acid is used in 3.0-24,0%concentration.

 

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