CN104194765A - Continuously blended liquefied polymer thickener for fracturing construction - Google Patents

Continuously blended liquefied polymer thickener for fracturing construction Download PDF

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Publication number
CN104194765A
CN104194765A CN201410429635.3A CN201410429635A CN104194765A CN 104194765 A CN104194765 A CN 104194765A CN 201410429635 A CN201410429635 A CN 201410429635A CN 104194765 A CN104194765 A CN 104194765A
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pressing crack
crack construction
construction according
continuous mixture
polymer viscosifier
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Inventor
何志勇
屈贺幂
牛增前
党伟
李青一
蔡景超
张秋红
马如然
周勋
李伟
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CNPC Bohai Drilling Engineering Co Ltd
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CNPC Bohai Drilling Engineering Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/602Compositions for stimulating production by acting on the underground formation containing surfactants
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/602Compositions for stimulating production by acting on the underground formation containing surfactants
    • C09K8/604Polymeric surfactants
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/62Compositions for forming crevices or fractures
    • C09K8/66Compositions based on water or polar solvents
    • C09K8/68Compositions based on water or polar solvents containing organic compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/84Compositions based on water or polar solvents
    • C09K8/86Compositions based on water or polar solvents containing organic compounds
    • C09K8/88Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/882Compositions based on water or polar solvents containing organic compounds macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/84Compositions based on water or polar solvents
    • C09K8/86Compositions based on water or polar solvents containing organic compounds
    • C09K8/88Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/90Compositions based on water or polar solvents containing organic compounds macromolecular compounds of natural origin, e.g. polysaccharides, cellulose

Abstract

The invention discloses a continuously blended liquefied polymer thickener for fracturing construction. The liquid polymer comprises a hydrophilic polymer, a hydrophobic oily organic solvent and other additives, wherein the additives comprise quaternary ammonium modified organic clay, a polar solvent and a surfactant. The liquid polymer is prepared by feeding each component according to a certain feeding sequence and stirring. The prepared liquid polymer can be rapidly dissolved or swollen in water and can be used as the thickener in the fracturing fluid.

Description

Be used for the liquefaction polymer viscosifier of the continuous mixture of pressing crack construction
Technical field
The present invention relates to a kind of polymer viscosifier for pressing crack construction, in particular for the liquefaction polymer viscosifier of the continuous mixture of pressing crack construction.
Background technology
In oilfield exploitation procedure, pressing crack construction has become transformation storage and has increased the requisite ring of output.In pressing crack construction process, workmen need to use a large amount of fluids, and we are referred to as fracturing liquid conventionally; This fluid is transported to pit shaft by high-pressure pump by ground, and produces pressure (effect of liquid pressure transmission) at pit shaft; In the time that the pressure producing is greater than the terrestrial stress of the borehole wall and tensile strength of rock, the borehole wall has just produced crack.These newly-generated cracks provide oil gas to enter the passage of pit shaft.In order to keep these cracks, we need to add propping agent in fracturing liquid, such as sandstone, ceramic particle, high-intensity polymer materials etc.These propping agents are along with fracturing liquid enters and remains in crack, to bear reservoir pressure; After stopping pumping fracturing liquid, due to the existence of propping agent, crack just can be not closed under the effect of reservoir pressure.Carry the fracturing liquid of these propping agents can be divided into two types: the first is the aqueous fracturing fluid with water compositing dispersion medium; The second is the oil base fracturing fluid using oil phase as dispersion medium.Aqueous fracturing fluid has the following advantages compared with oil base fracturing fluid: 1) production cost lower (water is more cheap than oil), 2) safety performance higher (oil can burn).Therefore, the application of aqueous fracturing fluid is more extensive.In order to transmit pressure, fracturing stratum, carries propping agent, and fracturing liquid must have certain viscosity.Current, in aqueous fracturing fluid, conventionally contain a certain proportion of wetting ability thickening material and carry out adjusting viscosity.This thickening material uses waterborne polymeric conventionally, such as guanidine glue, Mierocrystalline cellulose, xanthan gum, guanidine gum derivative, derivatived cellulose, xanthan derivatives etc.Itself can increase liquid viscosity these polymkeric substance, then has added after linking agent, and the viscosity of its aqueous solution can further improve.
The compound method of above-mentioned waterborne polymeric or the fluid of other polymkeric substance can be the method for batch mixed or the method for continuous mixture.The implication of batch mixed is: before pumping into down-hole, polymkeric substance and additive (such as sterilant, polymkeric substance, inorganic salt, buffer reagent, acid or alkali, clay stabilizer etc.) mix with water in material-compound tank; Mix and leave standstill later for some time, until polymkeric substance aquation in water completely.Batch mixed can ensure the quality of configured liquid, but has also caused the waste of material.This is owing to there being certain parameter in site operation process, these parameters cause final consumption that cannot accurate calculation liquid, therefore, designer is calculating and on the basis of spent material, can add certain safe clearance, and the increase of these safety using amounts has caused waste.Boring in completion technique service industry, the severe challenge that the continuous rising Ye Shi enterprise of cost faces always.The method of batch mixed, except waste material, also causes the rising of cost.Adopt in the process of batch mixed method preparing fracturing fluid, well site needs a large amount of liquid of storage and maintenance, and this has just caused high cost; The existence of safe clearance, causes again the further raising of cost.Mixture is also a kind of burden to environment protection in batches.Ecological environmental protection requires zero waste in process of production without abandoning.But in the engineering of batch mixed method preparing fracturing fluid, a large amount of residual liquid is often arranged at the bottom of material-compound tank, how processing these residues becomes the very thorny environment difficult problem that slip-stick artist need to face.Different from batch mixture, mixed technology is a kind of method that basis need to configure liquid in real time continuously.Mixed technology can overcome the easy waste of above-mentioned batch mixed technology continuously, and cost is high, the disagreeableness various shortcoming of environment.This real-time continuous mixed technology can measure the quantity of each material at the scene accurately, and it is unnecessary or residual can not produce in process of production.Mixed technology can be realized real-time formulated fluids continuously, according to adding in real time material, at utmost reduces the waste of material, reduces unnecessary cost.
In continuous mixed technology, workmen needs a kind of simple and quick method that measures thickening material.A very cost-effective method adopts pumping system exactly.Adopt pumping system can control the volume of fluid, also without adding extra equipment.But pumping system requires thickening material preferably to exist with liquid instead of with solid form.At present, thickening material, as guanidine glue, Mierocrystalline cellulose, xanthan gum, guanidine gum derivative, derivatived cellulose, xanthan derivatives, exists with solid state powder conventionally.These solid polymers are applied to continuous mixed technology following difficulty: 1) need to add extra control device and measure material; 2) disperse inhomogeneously, hydration rate is slow, 3) easily produce flake and caking.Therefore, how to overcome the above-mentioned shortcoming of solid-state thickening material, develop a kind of thickening material based on liquid polymer systems, become the problem that first continuous mixture and batch production pressure break must solve that realizes.
Summary of the invention
In order to overcome the various shortcoming that uses the existence of solid thickening material in fracturing liquid preparation and construction, meet the needs that Hydro Fracturing Stimulation Treatment scale expands gradually, realize continuous mixture and large-scale industrialized pressure break, the invention provides a kind of liquefaction polymer viscosifier of the continuous mixture for pressing crack construction.
In order to solve the problems of the technologies described above, the technical solution used in the present invention is: a kind of liquefaction polymer viscosifier of the continuous mixture for pressing crack construction, comprises the composition of following mass percent:
Described water-soluble polymers is one or more in polysaccharide, polysaccharide derivates and water-soluble synthesising macromolecule copolymer.
Described polysaccharide, polysaccharide derivates are one or more in guanidine glue, modification guanidine glue, Mierocrystalline cellulose, modified-cellulose, xanthan gum, modification xanthan gum, vegetable jelly, modified plant gum, starch and treated starch.
Described water-soluble synthesising macromolecule copolymer is one or both in polyacrylamide, polyacrylamide derivative.
Described hydrophobic nature oil phase solvent is one or more in mineral oil, diesel oil, white oil, whiteruss, gasoline, lubricating oil.
Described modification organic clay is the wilkinite of organic quaternary ammonium salt modification.
Described organic quaternary ammonium salt is two octadecyl Dimethyl Ammonium or cetyltrimethyl ammonium.
Described polar solvent is one or more in methyl alcohol, ethanol, formic acid and acetic acid.
Described tensio-active agent is one or more in amphoterics, anion surfactant, cats product and nonionogenic tenside.
Described tensio-active agent is one or more in alkylphenol polyoxyethylene, sorbitan trioleate, polyoxyethylene sorbitol acid anhydride trioleate.
The invention has the beneficial effects as follows: liquid polymers of the present invention is to be dispersed in preparation in oil phase by solid polymer to obtain.These dispersed polymkeric substance in oil phase are difficult for assembling, join after the aqueous solution, there will not be the phenomenon of " water bag powder ", overcome like this phenomenon of flake and caking, once polymkeric substance scatter completely in water, the speed of its aquation is decided by the water-retaining capacity of itself.
Brief description of the drawings
Fig. 1 organic clay powder X ray diffracting spectrum;
Flow curve after Fig. 2 hydroxypropyl guar is crosslinked;
Flow curve after Fig. 3 liquid polymeric matter sample 3 is crosslinked.
Embodiment
Below in conjunction with the drawings and specific embodiments, the present invention is described in further detail:
The present invention, for the liquefaction polymer viscosifier of the continuous mixture of pressing crack construction, comprises the composition of following mass percent:
Liquid polymer systems of the present invention is a kind of oil phase suspension system of waterborne polymeric.Polymkeric substance in this individual system is dispersed in hydrophobic nature solvent uniformly, and can aquation.Stable some additives (suspension agent/tensio-active agent) and the some other reagent adding as required of depending on of this suspension system.In these additives, tensio-active agent can help polymer dispersed and promote aquation.SURFACTANT ADSORPTION, on the surface of polymer beads, has reduced the avidity between polymer beads, helps polymer dispersed in oil phase.The dispersion in other words conj.or perhaps having shifted to an earlier date of this inherence, has optimized initial dispersion degree when polymkeric substance contacts with water, can avoid the caking of polymer beads in hydration process and the appearance of surface glue junction phenomena.Tensio-active agent also affects water, the interaction between oil and polymkeric substance three, and it can help to expel the oil content of polymer surfaces, promotes contacting of water molecules and polymkeric substance, thus the aquation of acceleration polymkeric substance.If do not use tensio-active agent, polymkeric substance will postpone to some extent with contacting of water molecules, and hydration rate will be slack-off.Once polymkeric substance disperses, it is very crucial that the hydration rate of polymkeric substance self becomes, and relevant with following factor: pH value, initial mechanical stir speed (S.S.), the size of polymer beads, the concentration of salt, the concentration of polymkeric substance etc.Therefore, in water, regulate pH value, or PH buffer reagent is added in suspension, can change the hydration rate of polymkeric substance.
Liquid polymers in the present invention is by the hydrophobic nature oil phase solvent of 40%-70% (mass ratio) the suspend waterborne polymeric of 22.8%-57.6% (mass ratio) and the mixture of other additives.In mixture, additive contains the polar solvent of 0.4%-1.2% conventionally, the tensio-active agent of 1%-3%, the modification organic clay of 1%-3%.Organic clay is to have processed wilkinite through organic quaternary ammonium salt, has close oil properties; Organic clay, as dispersion agent, helps waterborne polymeric powder to disperse in oil; Polar solvent, as auxiliary dispersants, can help the dispersion of organic clay; Tensio-active agent is to help to accelerate the aquation of polymkeric substance.
Waterborne polymeric of the present invention is including but not limited to following natural polymer or synthetic polymer: 1) polyose or polysaccharide derivates, as guanidine glue, modification guanidine glue, Mierocrystalline cellulose, modified-cellulose, xanthan gum, modification xanthan gum, vegetable jelly, modified plant gum, starch, treated starch etc.; 2) water-soluble synthesising macromolecule copolymer, as polyacrylamide, polyacrylamide derivative etc.In concrete enforcement, the size of polymeric powder particles is conventionally in 200 order left and right.Although the powder of particle waterborne polymeric more carefully will more easily be dispersed in oil phase, the present invention is equally applicable to the polymkeric substance that particle is larger, such as size is 30 purpose polymers.Waterborne polymeric of the present invention can be also any mixing of these 30 orders to 200 order arbitrary sizes and any kind polymkeric substance.The part by weight of the waterborne polymeric using in invention is 22.8%-57.6%.
But oil-based solvent of the present invention comprises and is not limited to following organic solvent: mineral oil, diesel oil, white oil, whiteruss, gasoline, lubricated wet goods.The molecular formula of these hydrophobic nature organic solvents is CnH2n+2 chain ene compound, such as paraffin, isoparaffin paraffin etc.; Molecular formula is CnH2n, such as gasoline, diesel oil, mineral oil, white oil etc.The fundamental characteristics of these organic solvents is hydrophobics, with water unmixing; Can not swelling or dissolving waterborne polymeric.Other oily substance can be animal oil, vegetables oil, carboxylic esters, malonic ester, long-chain alkyl alcohol (6 to 10 of carbon atoms) etc.Oil-based solvent of the present invention can be also any mixing of these oil-based solvents.The part by weight of the oily liquid using in invention is 40%-70%.
Organic clay of the present invention is a kind of bentonitic organic ammonium salt modified product, has close oil properties, can be used as dispersion agent, helps waterborne polymeric powder to disperse in oil.Conventionally organic clay is generated by wilkinite and quaternary ammonium salt reaction that can hydration swelling.
Polar solvent in the present invention is including but not limited to following organic solvent: methyl alcohol, ethanol or other alcohols materials, formic acid, acetic acid or other acids, or the mixture of these acids and alcohols material.
The organic clay using in the present invention can be that a certain organic clay can be also the mixing of several organic claies.The part by weight of the organic clay using in invention is 1%-3%.Organic clay is dispersed in the polar solvent that may need to add 0.4%-1.2% in the process of oil phase, such as methyl alcohol or ethanol etc.These polar solvents can help organic clay to disperse in organic solvent.
Tensio-active agent used in the present invention can be the material as Types Below: amphoterics, anion surfactant, cats product and nonionogenic tenside.But concrete tensio-active agent comprises and is not limited to following compound: sorbitol ester compounds, the sulfosuccinate etc. of the ether compound of nonionic ester compound, polyoxyethylene glycol Ester, polyoxyethylene, sorbitol ester compounds, ethoxylation.In these compounds, optimal is the ether compound of polyoxyethylene.
The tensio-active agent that the present invention uses can be also any mixing of these tensio-active agents.Conventionally, after mixing, the HLB value of tensio-active agent need to be adjusted to 10 left and right.The part by weight of the tensio-active agent using in invention is 1%-3%.
Embodiment 1: organic clay synthetic
1, organic clay sample A1's is synthetic
In 500 ml deionized water, add 100 grams of na-montmorillonites, vigorous stirring 10 minutes.In the suspension liquid generating, add 70 grams for the treatment of agent distearyl dimethyl ammonium chlorides, mixture is heated to 80~90 DEG C, and continue to stir 12 hours.The sedimentation and filtration that reaction generates, and by filtrate 100ml deionized water wash 3 times.Leach thing and be dried 24 hours at vacuum drying oven (90 DEG C), pulverize and obtain the organic clay A1 that altered contents is two octadecyl Dimethyl Ammonium.
2, organic clay sample A2's is synthetic
In 500 ml deionized water, add 100 grams of na-montmorillonites, vigorous stirring 10 minutes.In the suspension liquid generating, add 40 grams for the treatment of agent cetyl trimethylammonium bromides, mixture is heated to 80~90 DEG C, and continue to stir 12 hours.The sedimentation and filtration that reaction generates, and by 100 ml deionized water washing 3 times for filtrate.Leach thing and be dried 24 hours at vacuum drying oven (90 DEG C), pulverize and obtain the organic clay A2 that altered contents is cetyltrimethyl ammonium.
Embodiment 2: formula test
The preparation of reference sample 1
In 100 milliliters of wide-necked bottles, add the whiteruss (Tianjin Chemical Plant production) of 15.2 grams, the methyl alcohol of 0.18 gram, Surfactant OP-10 of 0.55 gram, vigorous stirring 10 minutes (1000 revs/min), continue to stir, slowly add the hydroxypropyl guar powder of 10.5 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain comparative sample 1.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
The preparation of reference sample 2
In 100ml wide-necked bottle, add the whiteruss (Tianjin Chemical Plant production) of 15.2 grams, the organic clay A1 of 0.41 gram, the methyl alcohol of 0.18 gram, vigorous stirring 10 minutes (1000 revs/min), continue to stir, slowly add the hydroxypropyl guar powder of 10.5 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain comparative sample 2.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
The preparation of sample 3
In 100ml wide-necked bottle, add the whiteruss (Tianjin Chemical Plant production) of 15.2 grams, the organic clay A1 of 0.41 gram, the methyl alcohol of 0.18 gram, the tensio-active agent alkylphenol polyoxyethylene (OP-10) of 0.55 gram, vigorous stirring 10 minutes (1000 revs/min), slowly adds the hydroxypropyl guar powder of 10.5 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 3.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
The preparation of sample 4
In 100ml wide-necked bottle, add the whiteruss (Tianjin Chemical Plant production) of 15.2 grams, the organic clay A1 of 0.41g, the methyl alcohol of 0.18 gram, the tensio-active agent (sorbitan trioleate (span-85) of 0.1g and the polyoxyethylene sorbitol acid anhydride trioleate (tween-85) of 0.45 gram) of 0.55 gram, vigorous stirring 10 minutes (1000 revs/min), slowly adds the hydroxypropyl guar powder of 10.5 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 4.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
Embodiment 3: the suspension test of polymkeric substance in whiteruss
The preparation of sample 5
In 100ml wide-necked bottle, add the whiteruss (Tianjin Chemical Plant production) of 15.2 grams, the organic clay A2 of 0.41g, the methyl alcohol of 0.18 gram, Surfactant OP-10 of 0.55 gram, vigorous stirring 10 minutes (1000 revs/min), continue to stir, slowly add the hydroxypropyl guar powder of 10.5 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 5.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
The preparation of sample 6
In 100ml wide-necked bottle, add the whiteruss (Tianjin Chemical Plant production) of 15.2g, the organic clay A1 of 0.41 gram, the methyl alcohol of 0.18 gram, Surfactant OP-10 of 0.55 gram, vigorous stirring 10 minutes (1000 revs/min), continue to stir, slowly add the hydroxypropyl guar powder of 7.5 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 6.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
The preparation of sample 7
In 100ml wide-necked bottle, add the whiteruss (Tianjin Chemical Plant production) of 15.2 grams, the organic clay A1 of 0.41 gram, the methyl alcohol of 0.18 gram, Surfactant OP-10 of 0.55 gram, vigorous stirring 10 minutes (1000 revs/min), continue to stir, slowly add the hydroxypropyl guar powder of 7.5 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 7.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
The preparation of sample 8
In 100 milliliters of wide-necked bottles, add the whiteruss (Tianjin Chemical Plant production) of 15.2 grams, the organic clay A1 of 0.41 gram, the methyl alcohol of 0.18 gram, Surfactant OP-10 of 0.55 gram, vigorous stirring 10 minutes (1000 revs/min), continue to stir, slowly add the polyacrylamide of 7.5 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 8.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
Embodiment 4: the suspension test of polymkeric substance in white oil
In 100ml wide-necked bottle, add No. 10 white oils of 18.9 grams, the organic clay A1 of 0.6 gram, the methyl alcohol of 0.18 gram, Surfactant OP-10 of 0.5 gram, vigorous stirring 10 minutes (1000 revs/min), continues to stir, and slowly adds the hydroxypropyl guar powder of 20 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 9.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
In 100ml wide-necked bottle, add No. 10 white oils of 18.9 grams, the organic clay A1 of 0.6 gram, the methyl alcohol of 0.18 gram, Surfactant OP-10 of 0.5 gram, vigorous stirring 10 minutes (1000 revs/min), continues to stir, and slowly adds the Vltra tears of 20 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 10.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
Embodiment 5: the suspension test of polymkeric substance in gasoline
In 100ml wide-necked bottle, add the gasoline of 18.7g, the organic clay A1 of 0.6 gram, the methyl alcohol of 0.24 gram, Surfactant OP-10 of 0.7 gram, vigorous stirring 10 minutes (1000 revs/min), continues to stir, and slowly adds the hydroxypropyl guar powder of 20g in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 11.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
Embodiment 6: the suspension test of polymkeric substance in white oil and gasoline mixed solvent
In 100 milliliters of wide-necked bottles, add white oil and 9.3 grams of gasoline of 10 grams, the organic clay A1 of 0.6 gram, the methyl alcohol of 0.1 gram, Surfactant OP-10 of 0.5 gram, vigorous stirring 10 minutes (1000 revs/min), continue to stir, slowly add the hydroxypropyl guar powder of 20 grams in mixing liquid.After reinforced, continue to stir 30 minutes, stop stirring, obtain sample 12.Sample is poured in graduated graduated cylinder, and observe phenomena, records layering and occurs 5% clear liquid and needed time of layering 20%.The results are shown in Table 1.
Embodiment 7: the rheology testing of liquid polymers
Hydroxypropyl guar is cross-linked and rheometer test (contrast)
In 100 ml waters, add the hydroxypropyl guar of 0.6 gram, stir 20 minutes, add the sodium hydroxide of 0.15 gram, stir 3 minutes, add the high-temperature cross-linking agent BZ-1 (Bohai Sea probing company) of 0.6 milliliter, being stirred to crosslinked sample can hang, and stops stirring, and measures 50 milliliters of crosslinked sample determination viscosity-temperature curves.Curve is shown in Fig. 2.
Liquid polymeric matter sample 3 is cross-linked and rheometer test
In 100ml water, add the liquid polymers of 1.5g, stir 20 minutes, add the sodium hydroxide of 0.15g, stir 3 minutes, add the high-temperature cross-linking agent BZ-1 (Bohai Sea probing company) of 0.6ml, being stirred to crosslinked sample can hang, and stops stirring, and measures the crosslinked sample determination viscosity-temperature curve of 50ml.Curve is shown in Fig. 3.
Fig. 1 is organic clay powder X ray diffracting spectrum.Figure middle and upper part component curve is the diffracting spectrum of the organic clay A1 of two octadecyl Dimethyl Ammonium, and figure lower middle portion curve is the diffracting spectrum of the property composition organic clay A2 that is cetyltrimethyl ammonium.
Fig. 2 is the flow curve after hydroxypropyl guar is cross-linked.In experimentation, sample was heated to 135 DEG C within 35 minutes, and maintains 55 minutes in 135 DEG C subsequently, record the viscosity changing conditions of sample.In figure, hydroxypropyl guar is at 135 DEG C, shears more than 55 minutes viscosity remains on 100mPas.
Fig. 3 is the flow curve after liquid polymeric matter sample 3 is cross-linked.In experimentation, sample was heated to 135 DEG C within 35 minutes, maintains 55 minutes at 135 DEG C subsequently, record the viscosity changing conditions of sample.In figure, liquid polymeric matter sample 3 is at 135 DEG C, shears more than 55 minutes viscosity remains on 100mPas.
Table 1: the stability test of the liquid polymers of different compositions
In sum, content of the present invention is not limited in the above-described embodiment, and the knowledgeable people in same area can propose easily other embodiment within technical director's thought of the present invention, but this embodiment comprises within the scope of the present invention.

Claims (10)

1. for a liquefaction polymer viscosifier for the continuous mixture of pressing crack construction, it is characterized in that, comprise the composition of following mass percent:
2. the liquefaction polymer viscosifier of the continuous mixture for pressing crack construction according to claim 1, is characterized in that, described water-soluble polymers is one or more in polysaccharide, polysaccharide derivates and water-soluble synthesising macromolecule copolymer.
3. the liquefaction polymer viscosifier of the continuous mixture for pressing crack construction according to claim 2, it is characterized in that, described polysaccharide, polysaccharide derivates are one or more in guanidine glue, modification guanidine glue, Mierocrystalline cellulose, modified-cellulose, xanthan gum, modification xanthan gum, vegetable jelly, modified plant gum, starch and treated starch.
4. the liquefaction polymer viscosifier of the continuous mixture for pressing crack construction according to claim 2, is characterized in that, described water-soluble synthesising macromolecule copolymer is one or both in polyacrylamide, polyacrylamide derivative.
5. the liquefaction polymer viscosifier of the continuous mixture for pressing crack construction according to claim 1, is characterized in that, described hydrophobic nature oil phase solvent is one or more in mineral oil, diesel oil, white oil, whiteruss, gasoline, lubricating oil.
6. the liquefaction polymer viscosifier of the continuous mixture for pressing crack construction according to claim 1, is characterized in that, described modification organic clay is the wilkinite of organic quaternary ammonium salt modification.
7. the liquefaction polymer viscosifier of the continuous mixture for pressing crack construction according to claim 6, is characterized in that, described organic quaternary ammonium salt is two octadecyl Dimethyl Ammonium or cetyltrimethyl ammonium.
8. the liquefaction polymer viscosifier of the continuous mixture for pressing crack construction according to claim 1, is characterized in that, described polar solvent is one or more in methyl alcohol, ethanol, formic acid and acetic acid.
9. the liquefaction polymer viscosifier of the continuous mixture for pressing crack construction according to claim 1, it is characterized in that, described tensio-active agent is one or more in amphoterics, anion surfactant, cats product and nonionogenic tenside.
10. the liquefaction polymer viscosifier of the continuous mixture for pressing crack construction according to claim 9, it is characterized in that, described tensio-active agent is one or more in alkylphenol polyoxyethylene, sorbitan trioleate, polyoxyethylene sorbitol acid anhydride trioleate.
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