CN107606638B - Superconducting liquid heating type fuel gasification system - Google Patents

Superconducting liquid heating type fuel gasification system Download PDF

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CN107606638B
CN107606638B CN201710796529.2A CN201710796529A CN107606638B CN 107606638 B CN107606638 B CN 107606638B CN 201710796529 A CN201710796529 A CN 201710796529A CN 107606638 B CN107606638 B CN 107606638B
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fuel
diglycolamine
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parts
superconducting
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CN107606638A (en
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黎兴志
吴家强
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Giant Hydrocarbon New Energy Technology Co Ltd
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Giant Hydrocarbon New Energy Technology Co Ltd
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Abstract

The present invention provides a superconducting liquid heating type fuel gasification system, comprising: the device comprises a fuel tank, a fuel pump, a superconducting liquid heating device, an ultrasonic generator, a compressed air generator, a dry filter, a Venturi pump, a pressure controller and a combustor; the top of the fuel tank is provided with a fuel inlet, a remote thermometer, a pressure gauge, an internal thread ball valve for the pressure gauge, a long pipe for the pressure gauge and a fuel gas outlet; the bottom of the fuel tank is provided with a fuel discharge hole, the fuel is conveyed to an ultrasonic generator through the fuel discharge hole by a fuel pump to generate atomized fuel, and the ultrasonic generator is connected with an atomizing nozzle and conveys the atomized fuel back to the top of the fuel tank; a water inlet and a water outlet are formed in the heating sleeve; the superconducting liquid heating device is provided with a superconducting liquid adding port, an emptying valve, a water return pipe and a water outlet pipe; the superconducting liquid heating device is filled with superconducting liquid.

Description

Superconducting liquid heating type fuel gasification system
Technical Field
the invention relates to the field of industrial gas, in particular to a superconducting liquid heating type fuel gasification system.
Technical Field
Combustible gas is used in various fields in actual life, for example, cutting gas, power generation, chemical industry, automobiles and other fields, and the reason is that combustible gas can generate a large amount of heat during combustion, so that energy can be saved, and meanwhile, the advantages of low cost, less pollution, high safety and the like can be achieved. The fuel gases with different components have different heat values and different application fields. For example, the gas for industrial cutting requires a high standard of calorific value, and the common industrial cutting gases are three of propane gas, propylene gas, or acetylene gas.
There are many devices for gasifying liquid fuel, some of which gasify fuel by heating gasification, ultrasonic atomization or bubbling heating gasification, and when gasifying fuel by heating, the heating temperature needs to be increased continuously to improve the gasification efficiency, but the increase of the heating temperature can cause the fuel to be changed in quality, thereby affecting the quality of gasified fuel; the bubbling heating gasification efficiency is lower than the ultrasonic atomization efficiency.
The invention provides a superconducting liquid heating type fuel gasification system which has high fuel gasification efficiency and low manufacturing cost and does not need manual maintenance after installation.
Disclosure of Invention
The invention provides a superconducting liquid heating type fuel gasification system,
the superconducting liquid heating type fuel gasification system comprises: the device comprises a fuel tank, a fuel pump, a superconducting liquid heating device, an ultrasonic generator, a compressed air generator, a dry filter, a Venturi pump, a pressure controller and a combustor;
the top of the fuel tank is provided with a fuel inlet, a remote thermometer, a pressure gauge, an internal thread ball valve for the pressure gauge, a long pipe for the pressure gauge and a fuel gas outlet; the fuel inlet is connected with an automatic feeding device; an anti-corrosion heat-insulation coating is arranged on the inner wall of the fuel tank; the preparation raw materials of the anti-corrosion heat-insulation coating comprise the following components in parts by weight: 50-60 parts by weight of modified polyethylene, 80 parts by weight of water and 5-10 parts by weight of thickening agent;
A liquid level sensor is arranged on the inner wall of the fuel tank; a gas concentration sensor is arranged on the inner wall of the tank top of the fuel tank; an atomization nozzle is arranged in the tank of the fuel tank;
The outer wall of the fuel tank is provided with an anti-corrosion heat transfer coating, a heating sleeve and a liquid level meter; the preparation raw materials of the anti-corrosion heat transfer coating comprise the following components in parts by weight: 40-80 parts of modified silicon dioxide, 1-5 parts of graphene oxide and 20-40 parts of solvent;
The bottom of the fuel tank is provided with a fuel discharge hole, the fuel is conveyed to an ultrasonic generator through the fuel discharge hole by a fuel pump to generate atomized fuel, and the ultrasonic generator is connected with an atomizing nozzle and conveys the atomized fuel back to the top of the fuel tank; a water inlet and a water outlet are formed in the heating sleeve;
the superconducting liquid heating device is provided with a superconducting liquid adding port, an emptying valve, a water inlet and a water outlet; the superconducting liquid heating device is internally provided with superconducting liquid, and the superconducting liquid comprises the following raw materials in percentage by mass: 0.5 to 5 percent of diglycolamine, 0.01 to 1 percent of sodium polyphosphate, 0.3 to 0.7 percent of benzotriazole derivative, 0.1 to 1.0 percent of sodium nitrite, 1 to 20 percent of modified diglycolamine and the balance of water; the superconducting liquid heating device heats the fuel in the fuel tank; the inner wall of the fuel tank is provided with a liquid level sensor for monitoring the content of the liquid fuel in the fuel tank, and the automatic feeding device can automatically feed when the liquid fuel is too low; a gas concentration sensor is arranged on the inner wall of the tank top of the fuel tank and used for sensing the concentration of gasified fuel, and the superconducting liquid heating device is connected with a water return pipe and a water outlet pipe; the gas outlet and the compressed air generator are connected with the combustor through a Venturi pump; a drying filter is arranged between the compressed air generator and the Venturi pump and is used for drying and filtering compressed air; and a pressure controller is arranged between the Venturi pump and the combustor and used for controlling and adjusting the proportion between the compressed air and the atomized fuel.
as an embodiment of the present invention, the superconducting liquid comprises, by mass: 0.5 to 2 percent of diglycolamine, 0.01 to 0.5 percent of sodium polyphosphate, 0.3 to 0.6 percent of benzotriazole derivative, 0.1 to 0.8 percent of sodium nitrite, 8 to 18 percent of modified diglycolamine and the balance of water.
As an embodiment of the present invention, the benzotriazole derivative is dimethyl benzotriazole.
as an embodiment of the invention, the remote thermometer is WSSX-411.
in one embodiment of the invention, the raw materials for preparing the anti-corrosion thermal insulation coating comprise, by weight: 53 parts of modified polyethylene, 80 parts of water and 6 parts of thickening agent.
In one embodiment of the present invention, the raw materials for preparing the anti-corrosion heat transfer coating comprise, by weight: 63 parts by weight of modified silica, 5 parts by weight of graphene oxide and 35 parts by weight of a solvent.
As an embodiment of the present invention, the preparation method of the modified diglycolamine comprises:
S01: phenyl methacrylate and diglycolamine in a molar ratio of (1-3): 1, adding 8 wt% of sodium ethoxide as a catalyst, and reacting at 100 ℃ for 120h to obtain a phenyl methacrylate modified diglycolamine crude product;
s02: adding a phenyl methacrylate modified diglycolamine crude product and an organic solvent into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the phenyl methacrylate modified diglycolamine crude product is 3 wt% -10 wt%, cooling to normal temperature, then extracting the solution from the prepared solution by using an injector, fixing the injector filled with the phenyl methacrylate modified diglycolamine crude product solution on a sample rack of electrostatic spinning equipment, connecting a power supply anode with an injector needle, connecting a power supply cathode with a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a phenyl methacrylate modified diglycolamine pure product;
s03: reacting the pure product of phenyl methacrylate modified diglycolamine with polyamine to obtain the modified diglycolamine.
As an embodiment of the present invention, the ultrasonic generator atomizes the fuel into droplets having a particle size of 0.2 μm to 0.5 μm.
As an embodiment of the present invention, the superconducting liquid comprises, by mass: 2% of diglycolamine, 0.8% of sodium polyphosphate, 0.5% of benzotriazole derivative, 0.8% of sodium nitrite, 11% of modified diglycolamine and the balance of water.
drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below, it is obvious that the drawings in the following description are only some embodiments of the present invention, and for those skilled in the art, other drawings can be obtained according to the drawings without creative efforts.
FIG. 1: schematic connection of the fuel tank and superconducting fluid heating apparatus described in example 1.
FIG. 2: a schematic diagram of a superconducting liquid heated fuel gasification system according to embodiment 1.
FIG. 3: schematic structural diagram of superconducting fluid heating apparatus according to embodiment 1
FIG. 4: a schematic diagram of a superconducting liquid heated fuel gasification system according to embodiment 3.
FIG. 5: a schematic diagram of a superconducting liquid heated fuel gasification system according to embodiment 4.
FIG. 6: a schematic diagram of a superconducting liquid heated fuel gasification system according to embodiment 5.
FIG. 7: a schematic diagram of a superconducting liquid heated fuel gasification system according to embodiment 6.
FIG. 8: a schematic diagram of a superconducting liquid heated fuel vaporization system according to embodiment 7.
Description of the symbols: the device comprises a fuel tank 1, a fuel pump 2, a superconducting liquid heating device 3, an ultrasonic generator 4, a compressed air generator 5, a dry filter 6, a Venturi pump 7, a pressure controller 8, a burner 9, a fuel inlet 10, a remote thermometer 11, a pressure gauge 12, an internal thread ball valve 13 for the pressure gauge, a long pipe 14 for the pressure gauge, a fuel gas outlet 15, an anti-corrosion heat-preservation coating 16, a liquid level sensor 17, a gas concentration sensor 18, an atomizing nozzle 19, an anti-corrosion heat-transfer coating 20, a heating sleeve 21, a liquid level meter 22, a fuel discharge port 23, a super liquid guide adding port 24, an emptying valve 25, an emptying valve 26, a water return pipe 27, a water outlet pipe 28, an automatic feeding device 29, a water inlet 30, a water outlet 31, a gas-liquid separator 32, a gas collection tank 33, a gas collection.
Detailed Description
the disclosure may be understood more readily by reference to the following detailed description of preferred embodiments of the invention and the examples included therein. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. In case of conflict, the present specification, including definitions, will control.
the term "prepared from …" as used herein is synonymous with "comprising". The terms "comprises," "comprising," "includes," "including," "has," "having," "contains," "containing," or any other variation thereof, as used herein, are intended to cover a non-exclusive inclusion. For example, a composition, process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such composition, process, method, article, or apparatus.
The conjunction "consisting of …" excludes any unspecified elements, steps or components. If used in a claim, the phrase is intended to claim as closed, meaning that it does not contain materials other than those described, except for the conventional impurities associated therewith. When the phrase "consisting of …" appears in a clause of the subject matter of the claims rather than immediately after the subject matter, it defines only the elements described in the clause; other elements are not excluded from the claims as a whole.
when an amount, concentration, or other value or parameter is expressed as a range, preferred range, or as a range of upper preferable values and lower preferable values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or preferred value and any lower range limit or preferred value, regardless of whether ranges are separately disclosed. For example, when a range of "1 to 5" is disclosed, the described range should be interpreted to include the ranges "1 to 4", "1 to 3", "1 to 2 and 4 to 5", "1 to 3 and 5", and the like. When a range of values is described herein, unless otherwise stated, the range is intended to include the endpoints thereof and all integers and fractions within the range.
The singular forms "a", "an" and "the" include plural referents unless the context clearly dictates otherwise. "optional" or "any" means that the subsequently described event or events may or may not occur, and that the description includes instances where the event occurs and instances where it does not.
approximating language, as used herein throughout the specification and claims, is intended to modify a quantity, such that the invention is not limited to the specific quantity, but includes portions that are literally received for modification without substantial change in the basic function to which the invention is related. Accordingly, the use of "about" to modify a numerical value means that the invention is not limited to the precise value. In some instances, the approximating language may correspond to the precision of an instrument for measuring the value. In the present description and claims, range limitations may be combined and/or interchanged, including all sub-ranges contained therein if not otherwise stated.
In addition, the indefinite articles "a" and "an" preceding an element or component of the invention are not intended to limit the number requirement (i.e., the number of occurrences) of the element or component. Thus, "a" or "an" should be read to include one or at least one, and the singular form of an element or component also includes the plural unless the stated number clearly indicates that the singular form is intended.
"Polymer" means a polymeric compound prepared by polymerizing monomers of the same or different types. The generic term "polymer" embraces the terms "homopolymer", "copolymer", "terpolymer" and "interpolymer".
"interpolymer" means a polymer prepared by polymerizing at least two different monomers. The generic term "interpolymer" includes the term "copolymer" (which is generally used to refer to polymers prepared from two different monomers) and the term "terpolymer" (which is generally used to refer to polymers prepared from three different monomers). It also includes polymers made by polymerizing four or more monomers. "blend" means a polymer formed by two or more polymers being mixed together by physical or chemical means.
The present invention provides a superconducting liquid heating type fuel gasification system, including: the device comprises a fuel tank, a fuel pump, a superconducting liquid heating device, an ultrasonic generator, a compressed air generator, a dry filter, a Venturi pump, a pressure controller and a combustor;
The top of the fuel tank is provided with a fuel inlet, a remote thermometer, a pressure gauge, an internal thread ball valve for the pressure gauge, a long pipe for the pressure gauge and a fuel gas outlet; the fuel inlet is connected with an automatic feeding device; an anti-corrosion heat-insulation coating is arranged on the inner wall of the fuel tank; the preparation raw materials of the anti-corrosion heat-insulation coating comprise the following components in parts by weight: 50-60 parts by weight of modified polyethylene, 80 parts by weight of water and 5-10 parts by weight of thickening agent;
a liquid level sensor is arranged on the inner wall of the fuel tank; a gas concentration sensor on an inner wall of a roof of the fuel tank; an atomization nozzle is arranged in the tank of the fuel tank;
The outer wall of the fuel tank is provided with an anti-corrosion heat transfer coating, a heating sleeve and a liquid level meter; the preparation raw materials of the anti-corrosion heat transfer coating comprise the following components in parts by weight: 40-80 parts of modified silicon dioxide, 1-5 parts of graphene oxide and 20-40 parts of solvent;
The bottom of the fuel tank is provided with a fuel discharge hole, the fuel is conveyed to an ultrasonic generator through the fuel discharge hole by a fuel pump to generate atomized fuel, and the ultrasonic generator is connected with an atomizing nozzle and conveys the atomized fuel back to the top of the fuel tank; a water inlet and a water outlet are formed in the heating sleeve;
the superconducting liquid heating device is provided with a superconducting liquid adding port, an emptying valve, a water inlet and a water outlet; the superconducting liquid heating device is internally provided with superconducting liquid, and the superconducting liquid comprises the following raw materials in percentage by mass: 0.5 to 5 percent of diglycolamine, 0.01 to 1 percent of sodium polyphosphate, 0.3 to 0.7 percent of benzotriazole derivative, 0.1 to 1.0 percent of sodium nitrite, 1 to 20 percent of modified diglycolamine and the balance of water; the gas outlet and the compressed air generator are connected to the burner by a venturi pump.
and a gas-liquid separator is arranged at the gas outlet.
As an embodiment of the present invention, the superconducting liquid comprises, by mass: 0.5 to 2 percent of diglycolamine, 0.01 to 0.5 percent of sodium polyphosphate, 0.3 to 0.6 percent of benzotriazole derivative, 0.1 to 0.8 percent of sodium nitrite, 8 to 18 percent of modified diglycolamine and the balance of water.
as an embodiment of the present invention, the benzotriazole derivative is dimethyl benzotriazole.
As an embodiment of the invention, the remote thermometer is WSSX-411.
In one embodiment of the invention, the raw materials for preparing the anti-corrosion thermal insulation coating comprise, by weight: 53 parts of modified polyethylene, 80 parts of water and 6 parts of thickening agent.
In one embodiment of the present invention, the raw materials for preparing the anti-corrosion heat transfer coating comprise, by weight: 63 parts by weight of modified silica, 5 parts by weight of graphene oxide and 35 parts by weight of a solvent.
As an embodiment of the present invention, the preparation method of the modified diglycolamine comprises:
s01: phenyl methacrylate and diglycolamine in a molar ratio of (1-3): 1, adding 8 wt% of sodium ethoxide as a catalyst, and reacting at 100 ℃ for 120h to obtain a phenyl methacrylate modified diglycolamine crude product;
s02: adding a phenyl methacrylate modified diglycolamine crude product and an organic solvent into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the phenyl methacrylate modified diglycolamine crude product is 3 wt% -10 wt%, cooling to normal temperature, then extracting the solution from the prepared solution by using an injector, fixing the injector filled with the phenyl methacrylate modified diglycolamine crude product solution on a sample rack of electrostatic spinning equipment, connecting a power supply anode with an injector needle, connecting a power supply cathode with a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a phenyl methacrylate modified diglycolamine pure product;
s03: reacting the pure product of phenyl methacrylate modified diglycolamine with polyamine to obtain the modified diglycolamine.
As an embodiment of the present invention, the ultrasonic generator atomizes the fuel into droplets having a particle size of 0.2 μm to 0.5 μm.
As an embodiment of the present invention, the superconducting liquid comprises, by mass: 2% of diglycolamine, 0.8% of sodium polyphosphate, 0.5% of benzotriazole derivative, 0.8% of sodium nitrite, 11% of modified diglycolamine and the balance of water.
Anti-corrosion heat-insulating coating
according to the invention, the preparation raw materials of the anti-corrosion heat-insulation coating comprise, by weight: 53 parts by weight of modified polyethylene, 80 parts by weight of water and 6 parts by weight of thickener.
modified polyethylene: the preparation method of the modified polyethylene comprises the following steps:
1. Pretreatment of polyethylene: adding polyethylene and toluene into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the polyethylene is 2-12 wt%, cooling to normal temperature, extracting the solution from the prepared solution by using an injector, fixing the injector filled with the polyethylene solution on a sample rack of electrostatic spinning equipment, connecting a positive electrode of a power supply with a needle of the injector, connecting a negative electrode of the power supply with a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a polyethylene crude product;
2. Dispersing the polyethylene crude product prepared in the step 1 into an ethanol solution, performing ultrasonic treatment for 30-60 minutes at room temperature, filtering, and drying at room temperature;
3. And (3) reacting the polyethylene crude product obtained in the step (2) with polyisocyanate to prepare the modified polyethylene.
Wherein, in the step 1,
the polyethylene was purchased from Shanghai plastic Rice information technology Co., Ltd., designation 2102TX 00.
The spinning time of the electrostatic spinning was 0.5 day.
the working voltage of the electrostatic spinning is 20 KV.
The spinneret-to-collector distance for the electrospinning was 20 cm.
The push speed of the sample feeding pump is 0.8 ml/h.
the spinneret for electrostatic spinning is a concentric circular double-nozzle, so that the modified polyethylene prepared by electrostatic spinning has a hollow tube structure.
in the step 3, the step of the method is that,
the polyisocyanate is selected from butane diisocyanate, pentane diisocyanate, hexamethylene diisocyanate, trimethyl hexamethylene diisocyanate, isophorone diisocyanate, hydrogenated xylylene diisocyanate, 1, 4-cyclohexane diisocyanate, p-phenylene diisocyanate, 1, 6-hexamethylene diisocyanate, dicyclohexylmethane diisocyanate, lysine diisocyanate, 2, 4-toluene diisocyanate, 2, 6-toluene diisocyanate, xylene-1, 4-diisocyanate, xylene-1, 3-diisocyanate, 4 ' -diphenylmethane diisocyanate, 2 ' -diphenylmethane diisocyanate, 4 ' -diphenyl ether diisocyanate, methyl ethyl phenyl diisocyanate, methyl propyl diisocyanate, methyl ethyl diisocyanate, 2-nitrodiphenyl-4, 4 '-diisocyanate, 2' -diphenylpropane-4, 4 '-diisocyanate, 3' -dimethyldiphenylmethane-4, 4 '-diisocyanate, 4' -diphenylpropane diisocyanate, naphthalene-1, 4-diisocyanate, naphthalene-1, 5-diisocyanate, 3 '-dimethoxydiphenyl-4, 4' -diisocyanate, isocyanate group-terminated hyperbranched polyurethane and isocyanate group-terminated polydimethylsiloxane.
in one embodiment of the present invention, the polyisocyanate is an isocyanate group-terminated hyperbranched polyurethane,
the term "isocyanate-terminated hyperbranched polyurethane" refers to a hyperbranched polyurethane terminated with isocyanate groups,
In a preferred embodiment, the method for preparing the isocyanate group-terminated hyperbranched polyurethane at least comprises the following steps:
(1) Dissolving isophorone diisocyanate and trimethylolethane in a dimethyl sulfoxide solvent respectively to obtain a diisocyanate solution and a trimethylolethane solution respectively;
(2) At 60 ℃, simultaneously performing nitrogen protection, adding a diisocyanate solution into a trimethylolethane solution, wherein the isocyanate group is excessive, and reacting the reaction system for 10 hours under the condition of heat preservation; heating to 100 ℃, and continuing to react for 12 h;
(3) And after the reaction is finished, carrying out reduced pressure distillation until no solvent exists, dissolving the obtained substance by tetrahydrofuran, settling in methanol, filtering, and carrying out vacuum drying at 80 ℃ for 15h to obtain the isocyanate group terminated hyperbranched polyurethane.
Further, isophorone diisocyanate, 1, 6-hexamethylene diisocyanate, lysine diisocyanate, and isocyanate group-terminated polydimethylsiloxane are all commercially available.
The reaction temperature in the step 3 is 100-: 1.
thickening agent: the thickening agent is selected from methyl cellulose purchased from Zhengzhou Jiahong chemical products, Inc., and the methoxyl content is 26-33%.
the preparation method of the anti-corrosion heat-insulation coating comprises the steps of mixing and stirring modified polyethylene and water at 40 ℃ for 3 hours, adding the thickening agent, and continuously stirring until the mixture is uniform.
Anti-corrosion heat transfer coating
The preparation raw materials of the anti-corrosion heat transfer coating comprise the following components in parts by weight: 63 parts by weight of modified silica, 5 parts by weight of graphene oxide, and 35 parts by weight of a solvent.
Modified silicon dioxide: the preparation method of the modified silicon dioxide comprises the following steps:
1. Preparation of silica: adding silicon dioxide and toluene into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the silicon dioxide is 1-25 wt%, cooling to normal temperature, adding polyvinylpyrrolidone and distilled water under stirring, cooling to normal temperature, stirring overnight, extracting the solution from the prepared solution by using an injector, fixing the injector filled with the silicon dioxide solution on a sample rack of electrostatic spinning equipment, connecting a positive electrode of a power supply with an injector needle, connecting a negative electrode of the power supply with a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a silicon dioxide crude product; calcining the crude silicon dioxide at high temperature, wherein the calcining temperature is 650 ℃, the temperature rise gradient is 1 ℃ per minute, the calcining time is 5 hours, and the cooling speed is 3 ℃ per minute;
2. dissolving the silica calcined in the step 1 in an ethanol solution, and stirring for 30 minutes under ultrasonic;
3. And (3) reacting the silicon dioxide obtained in the step (2) with polyisocyanate to prepare modified silicon dioxide.
Wherein, in the step 1,
The silica was purchased from Shanghai national drug, LLC of the national drug group.
the spinning of the electrospinning was carried out for 1 day.
the working voltage of the electrostatic spinning is 20 KV.
The spinneret-to-collector distance for the electrospinning was 20 cm.
The push speed of the sample feeding pump is 0.8 ml/h.
The spinneret for electrostatic spinning is a circular single nozzle, so that the modified silicon dioxide prepared by electrostatic spinning is in a fiber structure.
In the step 3, the step of the method is that,
The polyisocyanate is isocyanate group-terminated hyperbranched polyurethane,
The term "isocyanate-terminated hyperbranched polyurethane" refers to a hyperbranched polyurethane terminated with isocyanate groups,
In a preferred embodiment, the method for preparing the isocyanate group-terminated hyperbranched polyurethane at least comprises the following steps:
(1) Dissolving isophorone diisocyanate and trimethylolethane in a dimethyl sulfoxide solvent respectively to obtain a diisocyanate solution and a trimethylolethane solution respectively;
(2) at 60 ℃, simultaneously performing nitrogen protection, adding a diisocyanate solution into a trimethylolethane solution, wherein the isocyanate group is excessive, and reacting the reaction system for 10 hours under the condition of heat preservation; heating to 100 ℃, and continuing to react for 12 h;
(3) And after the reaction is finished, carrying out reduced pressure distillation until no solvent exists, dissolving the obtained substance by tetrahydrofuran, settling in methanol, filtering, and carrying out vacuum drying at 80 ℃ for 15h to obtain the isocyanate group terminated hyperbranched polyurethane.
further, isophorone diisocyanate, 1, 6-hexamethylene diisocyanate, lysine diisocyanate, and isocyanate group-terminated polydimethylsiloxane are all commercially available.
The reaction temperature in the step 3 is 100-: 1.
Solvent: the solvent is absolute ethyl alcohol.
Superconducting liquid: as an embodiment of the present invention, the superconducting liquid comprises, by mass: 1.2% of diglycolamine, 0.3% of sodium polyphosphate, 0.5% of benzotriazole derivative, 0.3% of sodium nitrite, 15% of modified diglycolamine and the balance of water.
diglycolamine: C4H11NO2, CAS number 929-06-6, available from Shanghai Demao chemical Co., Ltd.
Sodium polyphosphate: the sodium polyphosphate is prepared from sodium dipolyphosphate and sodium tripolyphosphate according to the weight ratio of 1: 2, or a mixture thereof.
The sodium dimeric phosphate and the sodium tripolyphosphate are purchased from Shanghai Limited company of the national drug group.
benzotriazole derivatives: the benzotriazole derivative is dimethyl benzotriazole, specifically 5, 7-dimethyl-1H-benzotriazole, has a CAS number of 49636-63-7, and is purchased from ArchBioscience company.
Sodium nitrite: the chemical formula is NaNO2, the CAS number is 7632-00-0, and the product is purchased from Shanghai Limited company of the national drug group.
Modified diglycolamine: the preparation method of the modified diglycolamine comprises the following steps:
s01: phenyl methacrylate and diglycolamine in a molar ratio of (1-3): 1, adding 8 wt% of sodium ethoxide as a catalyst, and reacting at 100 ℃ for 120h to obtain a phenyl methacrylate modified diglycolamine crude product;
S02: adding a phenyl methacrylate modified diglycolamine crude product and an organic solvent into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the phenyl methacrylate modified diglycolamine crude product is 3 wt% -10 wt%, cooling to normal temperature, then extracting the solution from the prepared solution by using an injector, fixing the injector filled with the phenyl methacrylate modified diglycolamine crude product solution on a sample rack of electrostatic spinning equipment, connecting a power supply anode with an injector needle, connecting a power supply cathode with a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a phenyl methacrylate modified diglycolamine pure product;
S03: reacting the pure product of phenyl methacrylate modified diglycolamine with polyamine to obtain the modified diglycolamine.
The preparation method of the superconducting liquid comprises the following steps:
a. weighing diglycolamine, sodium nitrite, modified diglycolamine and water according to the component proportion of the superconducting liquid, stirring and mixing at 20-25 ℃, and controlling the stirring speed to be more than 500 revolutions per minute;
b. standing and precipitating the stirred materials in the step a, and then stirring again until the materials are uniformly mixed for later use;
c. B, sequentially adding the rest components into the material obtained in the step b in no sequence, adding another component after each component is added, stirring and uniformly mixing until the last component is added, and uniformly mixing to obtain superconducting liquid;
d. And c, hermetically storing the superconducting fluid obtained in the step c in a refrigeration house.
Another aspect of the invention provides a process of the superconducting liquid heated fuel gasification system: the fuel in the fuel tank is output through the fuel discharge port and is conveyed to the ultrasonic generator through the fuel pump, atomized fuel is generated through the ultrasonic generator, the generated atomized fuel is conveyed back to the fuel tank through the atomizing nozzle, the fuel discharge port is arranged at the top of the fuel tank, the atomized fuel is output through the fuel discharge port and is mixed with compressed air generated by the compressed air generator, and the atomized fuel is conveyed to the combustor through the Venturi pump. A drying filter is arranged between the compressed air generator and the Venturi pump and is used for drying and filtering compressed air; and a pressure controller is arranged between the Venturi pump and the combustor and used for controlling and adjusting the proportion between the compressed air and the atomized fuel. The superconducting liquid heating device heats the fuel in the fuel tank to promote the gasification of the fuel; the inner wall of the fuel tank is provided with a liquid level sensor for monitoring the content of the liquid fuel in the fuel tank, and the automatic feeding device can automatically feed when the liquid fuel is too low; and a gas concentration sensor is arranged on the inner wall of the tank top of the fuel tank and used for sensing the concentration of the gasified fuel. The inner wall of the fuel tank is provided with an anti-corrosion heat-preservation coating, and the outer wall of the fuel tank is provided with an anti-corrosion heat-transfer coating for preventing corrosion and heat preservation of the fuel tank and rapid heat transfer of the superconducting liquid.
preferred embodiments of the present invention will be described in detail below with reference to the accompanying drawings.
example 1: this embodiment provides a superconducting liquid heating type fuel gasification system, including: the device comprises a fuel tank 1, a fuel pump 2, a superconducting liquid heating device 3, an ultrasonic generator 4, a compressed air generator 5, a dry filter 6, a venturi pump 7, a pressure controller 8 and a combustor 9;
The top of the fuel tank 1 is provided with a fuel inlet 10, a remote thermometer 11, a pressure gauge 12, an internal thread ball valve 13 for the pressure gauge, a long pipe 14 for the pressure gauge and a fuel gas outlet 15; an anti-corrosion heat-preservation coating 16 is arranged on the inner wall of the fuel tank 1;
A liquid level sensor 17 is arranged on the inner wall of the fuel tank 1; a gas concentration sensor 18 is arranged on the inner wall of the tank top of the fuel tank 1; an atomizing nozzle 19 is arranged in the tank of the fuel tank 1;
the outer wall of the fuel tank 1 is provided with an anti-corrosion heat transfer coating 20, a heating jacket 21 and a liquid level meter 22;
the bottom of the fuel tank 1 is provided with a fuel outlet 23, the fuel is delivered to an ultrasonic generator 4 through the fuel outlet 23 via a fuel pump 2 to generate atomized fuel, and the ultrasonic generator 4 is connected with an atomizing nozzle 19 to deliver the atomized fuel back to the top of the fuel tank 1; the heating jacket 21 is provided with a water inlet 30 and a water outlet 31;
The superconducting liquid heating device 3 is provided with a superconducting liquid adding port 24, an emptying valve 25, an emptying valve 26, a water inlet 30 and a water outlet 31;
The model of the remote thermometer 11 is WSSX-411.
the fuel inlet 10 is connected with an automatic feeding device 29;
the gas outlet 15 and the compressed-air generator 5 are connected to the burner 9 via a venturi pump 7. And a gas-liquid separator is arranged at the gas outlet.
in this embodiment, the raw materials for preparing the anti-corrosion thermal insulation coating comprise, by weight: 53 parts by weight of modified polyethylene, 80 parts by weight of water and 6 parts by weight of thickener.
Modified polyethylene: the preparation method of the modified polyethylene comprises the following steps:
1. Pretreatment of polyethylene: adding polyethylene and toluene into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the polyethylene is 5 wt%, cooling to normal temperature, extracting the solution from the prepared solution by using an injector, fixing the injector filled with the polyethylene solution on a sample rack of electrostatic spinning equipment, connecting a power supply anode with an injector needle, connecting a power supply cathode with a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a polyethylene crude product;
2. Dissolving the polyethylene crude product prepared in the step 1 in an ethanol solution, performing ultrasonic treatment for 60 minutes at room temperature, filtering, and drying at room temperature;
3. And (3) reacting the polyethylene crude product obtained in the step (2) with polyisocyanate to prepare the modified polyethylene.
wherein, in the step 1,
The polyethylene was purchased from Shanghai plastic Rice information technology Co., Ltd., designation 2102TX 00.
the spinning time of the electrostatic spinning was 0.5 day.
The working voltage of the electrostatic spinning is 20 KV.
The spinneret-to-collector distance for the electrospinning was 20 cm.
the push speed of the sample feeding pump is 0.8 ml/h.
The spinneret for electrostatic spinning is a concentric circular double-nozzle, so that the modified polyethylene prepared by electrostatic spinning has a hollow tube structure.
in step 3, the polyisocyanate is isocyanate group-terminated hyperbranched polyurethane, and the preparation method of the isocyanate group-terminated hyperbranched polyurethane at least comprises the following steps:
(1) Dissolving isophorone diisocyanate and trimethylolethane in a dimethyl sulfoxide solvent respectively to obtain a diisocyanate solution and a trimethylolethane solution respectively;
(2) At 60 ℃, simultaneously performing nitrogen protection, adding a diisocyanate solution into a trimethylolethane solution, wherein the isocyanate group is excessive, and reacting the reaction system for 10 hours under the condition of heat preservation; heating to 100 ℃, and continuing to react for 12 h;
(3) and after the reaction is finished, carrying out reduced pressure distillation until no solvent exists, dissolving the obtained substance by tetrahydrofuran, settling in methanol, filtering, and carrying out vacuum drying at 80 ℃ for 15h to obtain the isocyanate group terminated hyperbranched polyurethane.
further, isophorone diisocyanate, 1, 6-hexamethylene diisocyanate, lysine diisocyanate, and isocyanate group-terminated polydimethylsiloxane are all commercially available.
The reaction temperature of the step 3 is 110 ℃, the reaction time is 5 hours, and the weight ratio of the polyisocyanate to the modified polyethylene is 8: 1.
Thickening agent: the thickening agent is selected from methyl cellulose purchased from Zhengzhou Jiahong chemical products, Inc., and the methoxyl content is 26-33%.
The preparation method of the anti-corrosion heat-insulation coating comprises the steps of mixing and stirring modified polyethylene and water at 40 ℃ for 3 hours, adding the thickening agent, and continuously stirring until the mixture is uniform.
anti-corrosion heat transfer coating
the preparation raw materials of the anti-corrosion heat transfer coating comprise the following components in parts by weight: 63 parts by weight of modified silica, 5 parts by weight of graphene oxide, and 35 parts by weight of a solvent.
modified silicon dioxide: the preparation method of the modified silicon dioxide comprises the following steps:
1. Preparation of silica: adding silicon dioxide and toluene into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the silicon dioxide is 15 wt%, cooling to normal temperature, adding polyvinylpyrrolidone and distilled water under stirring, cooling to normal temperature, stirring overnight, extracting the solution from the prepared solution by using an injector, fixing the injector filled with the silicon dioxide solution on a sample rack of electrostatic spinning equipment, connecting a power supply anode with an injector needle, connecting a power supply cathode with a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a silicon dioxide crude product; calcining the crude silicon dioxide at high temperature, wherein the calcining temperature is 650 ℃, the temperature rise gradient is 1 ℃ per minute, the calcining time is 5 hours, and the cooling speed is 3 ℃ per minute;
2. dissolving the silica calcined in the step 1 in an ethanol solution, and stirring for 30 minutes under ultrasonic;
3. And (3) reacting the silicon dioxide obtained in the step (2) with polyisocyanate to prepare modified silicon dioxide.
wherein, in the step 1,
the silica was purchased from Shanghai Limited liability company, national drug group.
the spinning of the electrospinning was carried out for 1 day.
The working voltage of the electrostatic spinning is 20 KV.
The spinneret-to-collector distance for the electrospinning was 20 cm.
the push speed of the sample feeding pump is 0.8 ml/h.
the spinneret for electrostatic spinning is a circular single nozzle, so that the modified silicon dioxide prepared by electrostatic spinning is in a fiber structure.
In the step 3, the step of the method is that,
the polyisocyanate is isocyanate group-terminated hyperbranched polyurethane,
The term "isocyanate-terminated hyperbranched polyurethane" refers to a hyperbranched polyurethane terminated with isocyanate groups.
in a preferred embodiment, the method for preparing the isocyanate group-terminated hyperbranched polyurethane at least comprises the following steps:
(1) dissolving isophorone diisocyanate and trimethylolethane in a dimethyl sulfoxide solvent respectively to obtain a diisocyanate solution and a trimethylolethane solution respectively;
(2) at 60 ℃, simultaneously performing nitrogen protection, adding a diisocyanate solution into a trimethylolethane solution, wherein the isocyanate group is excessive, and reacting the reaction system for 10 hours under the condition of heat preservation; heating to 100 ℃, and continuing to react for 12 h;
(3) And after the reaction is finished, carrying out reduced pressure distillation until no solvent exists, dissolving the obtained substance by tetrahydrofuran, settling in methanol, filtering, and carrying out vacuum drying at 80 ℃ for 15h to obtain the isocyanate group terminated hyperbranched polyurethane.
further, isophorone diisocyanate, 1, 6-hexamethylene diisocyanate, lysine diisocyanate, and isocyanate group-terminated polydimethylsiloxane are all commercially available.
The reaction temperature of the step 3 is 110 ℃, the reaction time is 4h, and the weight ratio of the polyisocyanate to the modified polyethylene is 7: 1.
solvent: the solvent is absolute ethyl alcohol.
superconducting liquid: as an embodiment of the present invention, the superconducting liquid comprises, by mass: 1.2% of diglycolamine, 0.3% of sodium polyphosphate, 0.5% of benzotriazole derivative, 0.3% of sodium nitrite, 15% of modified diglycolamine and the balance of water.
Diglycolamine: C4H11NO2, CAS number 929-06-6, available from Shanghai Demao chemical Co., Ltd.
Sodium polyphosphate: the sodium polyphosphate is prepared from sodium dipolyphosphate and sodium tripolyphosphate according to the weight ratio of 1: 2, or a mixture thereof.
The sodium dimeric phosphate and the sodium tripolyphosphate are purchased from Shanghai Limited company of the national drug group.
benzotriazole derivatives: the benzotriazole derivative is dimethyl benzotriazole, specifically 5, 7-dimethyl-1H-benzotriazole, has a CAS number of 49636-63-7, and is purchased from ArchBioscience company.
Sodium nitrite: the chemical formula is NaNO2, the CAS number is 7632-00-0, and the product is purchased from Shanghai Limited company of the national drug group.
Modified diglycolamine: the preparation method of the modified diglycolamine comprises the following steps:
S01: phenyl methacrylate and diglycolamine in a molar ratio of 1: 1, adding 8 wt% of sodium ethoxide as a catalyst, and reacting at 100 ℃ for 120h to obtain a phenyl methacrylate modified diglycolamine crude product;
S02: adding a phenyl methacrylate modified diglycolamine crude product and an organic solvent into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the phenyl methacrylate modified diglycolamine crude product is 6 wt%, cooling to normal temperature, extracting the solution from the prepared solution by using an injector, fixing the injector filled with the phenyl methacrylate modified diglycolamine crude product solution on a sample rack of electrostatic spinning equipment, connecting a power supply anode with an injector needle, connecting a power supply cathode with a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a phenyl methacrylate modified diglycolamine pure product;
s03: reacting the pure product of phenyl methacrylate modified diglycolamine with polyamine to obtain the modified diglycolamine.
the preparation method of the superconducting liquid comprises the following steps:
a. Weighing diglycolamine, sodium nitrite, modified diglycolamine and water according to the component proportion of the superconducting liquid, stirring and mixing at 20-25 ℃, and controlling the stirring speed to be more than 500 revolutions per minute;
b. standing and precipitating the stirred materials in the step a, and then stirring again until the materials are uniformly mixed for later use;
c. B, sequentially adding the rest components into the material obtained in the step b in no sequence, adding another component after each component is added, stirring and uniformly mixing until the last component is added, and uniformly mixing to obtain superconducting liquid;
d. and c, hermetically storing the superconducting fluid obtained in the step c in a refrigeration house.
another aspect of the invention provides a process of the superconducting liquid heated fuel gasification system: the fuel in the fuel tank is output through the fuel discharge port and is conveyed to the ultrasonic generator through the fuel pump, atomized fuel is generated through the ultrasonic generator, the generated atomized fuel is conveyed back to the fuel tank through the atomizing nozzle, the fuel discharge port is arranged at the top of the fuel tank, the atomized fuel is output through the fuel discharge port and is mixed with compressed air generated by the compressed air generator, and the atomized fuel is conveyed to the combustor through the Venturi pump. A drying filter is arranged between the compressed air generator and the Venturi pump and is used for drying and filtering compressed air; and a pressure controller is arranged between the Venturi pump and the combustor and used for controlling and adjusting the proportion between the compressed air and the atomized fuel. The superconducting liquid heating device heats the fuel in the fuel tank to promote the gasification of the fuel; the inner wall of the fuel tank is provided with a liquid level sensor for monitoring the content of the liquid fuel in the fuel tank, and the automatic feeding device can automatically feed when the liquid fuel is too low; and a gas concentration sensor is arranged on the inner wall of the tank top of the fuel tank and used for sensing the concentration of the gasified fuel. The inner wall of the fuel tank is provided with an anti-corrosion heat-preservation coating, and the outer wall of the fuel tank is provided with an anti-corrosion heat-transfer coating for preventing corrosion and heat preservation of the fuel tank and rapid heat transfer of the superconducting liquid.
Example 2: the difference from the embodiment 1 is that the inner wall of the fuel tank is not provided with an anti-corrosion heat preservation coating, and the outer wall of the fuel tank is not provided with an anti-corrosion heat transfer coating.
example 3: the difference from embodiment 1 is that the superconducting fluid heating type fuel vaporization system of the present embodiment does not include a superconducting fluid heating device.
example 4: the difference from embodiment 1 is that the superconducting liquid heated fuel vaporization system of the present embodiment does not include an ultrasonic generator, a fuel pump, and an atomizer.
Example 5: the difference from embodiment 1 is that the superconducting liquid heated fuel gasification system of the present embodiment does not include a compressed air generator and a dry filter.
example 6: the difference from embodiment 1 is that the superconducting liquid heated fuel vaporization system of the present embodiment does not include a dry filter.
Example 7: the difference from embodiment 1 is that in the superconducting liquid heating type fuel vaporizing system of the present embodiment, the atomizer is disposed outside the fuel tank, and the following is specifically described: the superconducting liquid heating type fuel gasification system in the embodiment comprises: the device comprises a fuel tank, a fuel pump, a gas collecting tank, a superconducting liquid heating device, an ultrasonic generator, a compressed air generator, a dry filter, a Venturi pump, a pressure controller and a combustor;
the top of the fuel tank is provided with a fuel inlet, a remote thermometer, a pressure gauge, an internal thread ball valve for the pressure gauge, a long pipe for the pressure gauge and a fuel gas outlet; an anti-corrosion heat-insulation coating is arranged on the inner wall of the fuel tank;
The gas outlet is connected with a gas collecting tank through a gas collecting pipeline, and an atomizing nozzle is arranged in the gas collecting tank;
A liquid level sensor is arranged on the inner wall of the fuel tank; a gas concentration sensor is arranged on the inner wall of the tank top of the fuel tank;
the outer wall of the fuel tank is provided with an anti-corrosion heat transfer coating, a heating sleeve and a liquid level meter;
The bottom of the fuel tank is provided with a fuel discharge port, the fuel is conveyed to an ultrasonic generator through the fuel discharge port by a fuel pump to generate atomized fuel, and the ultrasonic generator is connected with an atomizing nozzle and conveys the atomized fuel to a gas collecting tank; a water inlet and a water outlet are formed in the heating sleeve;
the top of the gas collecting tank is provided with a gas outlet, and the gas outlet is connected with the compressed air generator through a Venturi pump and a combustor;
The superconducting liquid heating device is provided with a superconducting liquid adding port, an emptying valve, a water inlet and a water outlet; the superconducting liquid heating device is filled with superconducting liquid.
example 8: the difference from the example 1 is that the modified polyethylene is replaced by the common polyethylene in the preparation of the anti-corrosion heat-preservation coating, and the common polyethylene is purchased from Shanghai plastic Rice information technology Co., Ltd, and is under the trade name 2102TX 00.
example 9: the difference from the example 1 is that in the raw materials for preparing the anti-corrosion heat-preservation coating, the preparation method of the modified polyethylene comprises the following steps:
1. dispersing the purchased polyethylene in ethanol solution, performing ultrasonic treatment at room temperature for 30-60 minutes, filtering, and drying at room temperature; the polyethylene was purchased from Shanghai plastic Rice information technology Co., Ltd, under the designation 2102TX 00;
2. reacting the polyethylene crude product obtained in the step 1 with polyisocyanate to prepare modified polyethylene; the selection of the polyisocyanate and the preparation conditions were the same as in example 1.
Example 10: the difference from the example 1 is that in the preparation of the raw material of the anticorrosion heat-preservation coating, the spinneret for electrostatic spinning is replaced by a round single nozzle in the process of preparing the modified polyethylene.
example 11: the difference from the embodiment 1 is that in the preparation of the modified polyethylene in the raw materials of the anticorrosion heat-preservation coating, the polyisocyanate is selected from isophorone diisocyanate.
example 12: the difference from the example 1 is that the modified silica is replaced by the general silica purchased from Shanghai national drug, LLC of the national drug group in the preparation of the anti-corrosion heat transfer coating.
example 13: the difference from the embodiment 1 is that in the raw materials for preparing the anti-corrosion heat transfer coating, the modified silicon dioxide is prepared by the following steps:
1. Dissolving the purchased silicon dioxide in an ethanol solution, and stirring for 30 minutes under ultrasonic;
2. The silica obtained in step 1 is reacted with polyisocyanate to prepare modified silica, and the specific selection and reaction conditions of the polyisocyanate are the same as those in example 1.
Example 14: the difference from the embodiment 1 is that in the raw materials for preparing the anti-corrosion heat transfer coating, the modified silicon dioxide is prepared by the following steps: adding purchased silicon dioxide and toluene into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the silicon dioxide is 1-25 wt%, cooling to normal temperature, adding polyvinylpyrrolidone and distilled water under stirring, cooling to normal temperature, stirring overnight, extracting the solution from the prepared solution by using an injector, fixing the injector filled with the silicon dioxide solution on a sample rack of electrostatic spinning equipment, connecting a power supply anode and an injector needle, connecting a power supply cathode and a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a silicon dioxide crude product; and calcining the crude silicon dioxide at high temperature, wherein the calcining temperature is 650 ℃, the temperature rise gradient is 1 ℃ per minute, the calcining time is 5 hours, and the cooling speed is 3 ℃ per minute.
Example 15: the difference from example 1 is that the superconducting fluid is prepared from a raw material which does not contain modified diglycolamine.
Example 16: the difference from the embodiment 1 is that the superconducting liquid is prepared from raw materials which do not contain benzotriazole derivatives.
Example 17: the difference from the embodiment 1 is that the benzotriazole derivative in the superconducting liquid preparation raw material is 5-methylbenzotriazole.
Example 18: the difference from the embodiment 1 is that the sodium polyphosphate in the raw material for preparing the superconducting liquid is pure sodium dimeric phosphate.
And (3) testing:
the following test 1 was adopted in examples 1 and 8 to 11:
after heating the fuel in the fuel tank to 80 ℃, the fuel was placed in a sealed container prepared from the fuel tank materials (including the anticorrosive heat-insulating layer) of examples 1 and 8 to 11 and a sealed container prepared from carbon steel for 24 hours, and the temperature after 24 hours was measured.
Table 1: test results of test 1
secondly, the following test 2 is adopted in the embodiment 1 and the embodiments 12 to 14:
testing the heat transfer performance: the fuel tanks of examples 1 and 12 to 14 were each charged with 25 ℃ fuel, the superconducting liquid heating apparatus of example 1 was used to heat the fuel in the fuel tank, the temperature of the fuel in the fuel tank was measured by a thermometer, the temperature of the superconducting liquid was 50 ℃, and the time taken for the fuel in the fuel tank to heat to 45 ℃ was measured.
Thirdly, the method comprises the following steps: the following test 3 was used in examples 1 and 15 to 18:
brass, carbon steel and cast iron were subjected to corrosion performance tests in the superconducting fluids of examples 1 and 15 to 18.
a level: the surface is smooth, has no spots and rust;
b stage: the surface is not smooth, has spots and is not rusted;
C level: the surface was not smooth, speckled, rusted.
fourthly, the method comprises the following steps: the following test 4 was used in examples 1 and 8 to 14:
the fuel tanks of examples 1 and 8 to 14 were subjected to corrosion performance test in water. (test conditions according to Standard GB 6458-86)
A level: the surface is smooth, has no spots and rust;
B stage: the surface is not smooth, has spots and is not rusted;
C level: the surface was not smooth, speckled, rusted.
Fifthly: example 1, examples 15-18 the following test 5 was taken:
3. Brass, carbon steel and cast iron were subjected to corrosion performance tests in the superconducting fluids of examples 1 and 15 to 18.
a level: the surface is smooth, has no spots and rust;
B stage: the surface is not smooth, has spots and is not rusted;
C level: the surface was not smooth, speckled, rusted.
Sixthly, the method comprises the following steps: example 1, examples 15-18 the following test 6 was taken:
The superconducting fluids of examples 1 and 15 to 18 were used, and the thermal conductivity thereof was measured at 30 ℃.
Seventhly, the method comprises the following steps: the following test 7 was conducted for examples 1 to 5:
testing the calorific value of the fuel-gasified gas conveyed from the gas outlet pipeline and the stability of the calorific value:
The above calorific value is given in Kcal. The stability test means that the calorific value of the gas discharged from the gas outlet pipe was measured 30 minutes after the superconducting liquid-heated fuel gasification system started to operate. The first data to be tested after the start of the operation for 30 minutes was "heat value at 0 second", the second data to be tested after the start of the operation for 30 minutes and 30 seconds was "heat value at 30 seconds", and so on.
The foregoing examples are illustrative only, and serve to explain some of the features of the present disclosure. The appended claims are intended to claim as broad a scope as is contemplated, and the examples presented herein are merely illustrative of selected implementations in accordance with all possible combinations of examples. Accordingly, it is applicants' intention that the appended claims are not to be limited by the choice of examples illustrating features of the invention. And that advances in science and technology will result in possible equivalents or sub-substitutes not currently contemplated for reasons of inaccuracy in language representation, and such changes should also be construed where possible to be covered by the appended claims.

Claims (9)

1. A superconducting liquid-heated fuel gasification system, comprising: the device comprises a fuel tank, a fuel pump, a superconducting liquid heating device, an ultrasonic generator, a compressed air generator, a dry filter, a Venturi pump, a pressure controller and a combustor;
The top of the fuel tank is provided with a fuel inlet, a remote thermometer, a pressure gauge, an internal thread ball valve for the pressure gauge, a long pipe for the pressure gauge and a fuel gas outlet; the fuel inlet is connected with an automatic feeding device; an anti-corrosion heat-insulation coating is arranged on the inner wall of the fuel tank; the preparation raw materials of the anti-corrosion heat-insulation coating comprise the following components in parts by weight: 50-60 parts by weight of modified polyethylene, 80 parts by weight of water and 5-10 parts by weight of thickening agent;
A liquid level sensor is arranged on the inner wall of the fuel tank; a gas concentration sensor is arranged on the inner wall of the tank top of the fuel tank; an atomization nozzle is arranged in the tank of the fuel tank;
the outer wall of the fuel tank is provided with an anti-corrosion heat transfer coating, a heating sleeve and a liquid level meter; the preparation raw materials of the anti-corrosion heat transfer coating comprise the following components in parts by weight: 40-80 parts of modified silicon dioxide, 1-5 parts of graphene oxide and 20-40 parts of solvent;
The bottom of the fuel tank is provided with a fuel discharge hole, the fuel is conveyed to an ultrasonic generator through the fuel discharge hole by a fuel pump to generate atomized fuel, and the ultrasonic generator is connected with an atomizing nozzle and conveys the atomized fuel back to the top of the fuel tank; a water inlet and a water outlet are formed in the heating sleeve;
The superconducting liquid heating device is provided with a superconducting liquid adding port, an emptying valve, a water inlet and a water outlet; the superconducting liquid heating device is internally provided with superconducting liquid, and the superconducting liquid comprises the following raw materials in percentage by mass: 0.5 to 5 percent of diglycolamine, 0.01 to 1 percent of sodium polyphosphate, 0.3 to 0.7 percent of benzotriazole derivative, 0.1 to 1.0 percent of sodium nitrite, 1 to 20 percent of modified diglycolamine and the balance of water; the superconducting liquid heating device heats the fuel in the fuel tank; the inner wall of the fuel tank is provided with a liquid level sensor for monitoring the content of the liquid fuel in the fuel tank, and the automatic feeding device can automatically feed when the liquid fuel is too low; a gas concentration sensor is arranged on the inner wall of the tank top of the fuel tank and used for sensing the concentration of gasified fuel, and the superconducting liquid heating device is connected with a water return pipe and a water outlet pipe; the gas outlet and the compressed air generator are connected with the combustor through a Venturi pump; a drying filter is arranged between the compressed air generator and the Venturi pump and is used for drying and filtering compressed air; and a pressure controller is arranged between the Venturi pump and the combustor and used for controlling and adjusting the proportion between the compressed air and the atomized fuel.
2. The superconducting fluid heated fuel gasification system of claim 1, wherein the superconducting fluid is prepared from a raw material comprising, in mass percent: 0.5 to 2 percent of diglycolamine, 0.01 to 0.50 percent of sodium polyphosphate, 0.3 to 0.6 percent of benzotriazole derivative, 0.1 to 0.8 percent of sodium nitrite, 8 to 18 percent of modified diglycolamine and the balance of water.
3. the superconducting liquid heating type fuel gasification system according to claim 1, wherein the benzotriazole derivative is dimethyl benzotriazole.
4. The superconducting liquid heated fuel gasification system of claim 1, wherein the remote thermometer is model number WSSX-411.
5. The superconducting liquid heating type fuel gasification system according to claim 1, wherein the raw material for preparing the corrosion-proof heat-insulating coating comprises, in parts by weight: 53 parts of modified polyethylene, 80 parts of water and 6 parts of thickening agent.
6. the superconducting liquid heating type fuel gasification system of claim 1, wherein the raw material for preparing the anti-corrosion heat transfer coating comprises, in parts by weight: 63 parts by weight of modified silica, 5 parts by weight of graphene oxide, and 35 parts by weight of a solvent.
7. The superconducting liquid heating type fuel gasification system according to claim 1, wherein the modified diglycolamine is prepared by a method comprising:
s01: phenyl methacrylate and diglycolamine in a molar ratio of (1-3): 1, adding 8 wt% of sodium ethoxide as a catalyst, and reacting at 100 ℃ for 120h to obtain a phenyl methacrylate modified diglycolamine crude product;
s02: adding a phenyl methacrylate modified diglycolamine crude product and an organic solvent into a flask, heating and dissolving under stirring to prepare a solution, wherein the concentration of the phenyl methacrylate modified diglycolamine crude product is 3 wt% -10 wt%, cooling to normal temperature, then extracting the solution from the prepared solution by using an injector, fixing the injector filled with the phenyl methacrylate modified diglycolamine crude product solution on a sample rack of electrostatic spinning equipment, connecting a power supply anode with an injector needle, connecting a power supply cathode with a collector, starting a sample injection pump, turning on a high-voltage power supply to carry out electrostatic spinning, turning off the high-voltage power supply, the sample injection pump and the collector after the electrostatic spinning is finished, stopping spinning, and collecting a phenyl methacrylate modified diglycolamine pure product;
s03: reacting the pure product of phenyl methacrylate modified diglycolamine with polyamine to obtain the modified diglycolamine.
8. The superconducting liquid heated fuel gasification system of claim 1, wherein the ultrasonic generator atomizes the fuel into droplets having a size of 0.2 μm to 0.5 μm.
9. The superconducting fluid heated fuel gasification system of claim 1, wherein the superconducting fluid is prepared from a raw material comprising, in mass percent: 2% of diglycolamine, 0.8% of sodium polyphosphate, 0.5% of benzotriazole derivative, 0.8% of sodium nitrite, 11% of modified diglycolamine and the balance of water.
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