CN115216124B - High-dispersion aerogel master batch and preparation method and application thereof - Google Patents

High-dispersion aerogel master batch and preparation method and application thereof Download PDF

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CN115216124B
CN115216124B CN202210552954.8A CN202210552954A CN115216124B CN 115216124 B CN115216124 B CN 115216124B CN 202210552954 A CN202210552954 A CN 202210552954A CN 115216124 B CN115216124 B CN 115216124B
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aerogel
master batch
powder
paste
resin matrix
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CN115216124A (en
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孙光耀
鲁祥凯
杨军辉
谢伟
云山
朱鹏
王继业
任天斌
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Poly Plastic Masterbatch Suzhou Co ltd
Jiangsu Jicui Functional Material Research Institute Co ltd
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Poly Plastic Masterbatch Suzhou Co ltd
Jiangsu Jicui Functional Material Research Institute Co ltd
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • C08J3/22Compounding polymers with additives, e.g. colouring using masterbatch techniques
    • C08J3/226Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2467/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2467/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2258Oxides; Hydroxides of metals of tungsten

Abstract

The application relates to the field of heat preservation and insulation materials, in particular to the technical field of C04B38/08, and more particularly relates to a high-dispersion aerogel fiber master batch and a preparation method and application thereof. The high-dispersion aerogel master batch is prepared by mixing aerogel paste material and a resin matrix; the weight ratio of aerogel paste to resin matrix is 1: (0.5-10); the content of aerogel powder in the aerogel master batch is 0.35-13 wt%; the aerogel powder in the aerogel master batch accounts for 0.4 to 29.5 weight percent of the resin matrix. The aerogel paste material and the resin matrix with the density matched are adopted for mixing and granulating, so that the problem of dispersion caused by too low density of the aerogel is solved, meanwhile, the problems of difficult blanking and the like in the process of preparing the master batch are avoided, and the obtained aerogel master batch has good formability, heat preservation and insulation performance and processability. The method can realize the preparation of multi-concentration multi-type heat preservation and insulation master batch, and form rich series products.

Description

High-dispersion aerogel master batch and preparation method and application thereof
Technical Field
The application relates to the field of heat preservation and insulation materials, in particular to the technical field of C04B38/08, and more particularly relates to a high-dispersion aerogel fiber master batch and a preparation method and application thereof.
Background
Aerogel is a material with 'infinite' nano-scale holes, and extremely high porosity leads to extremely low density and heat conductivity coefficient, so that the aerogel has great application potential in the field of heat insulation. At present, in the research and development of thermal fibers in the textile field, new paths are explored at home and abroad, namely aerogel and chemical fibers are combined to prepare fibers. The functional master batch is prepared by blending aerogel powder and plastic powder, and the aerogel is too light, so that the dispersion is poor, and various problems such as difficult discharging or uneven granules occur in the granulating process. In addition, along with the increase of people to environmental protection demand, the conventional aerogel powder that adopts directly mixes granulation with the material can cause dust pollution, has various potential risks. Therefore, exploring an aerogel to be mixed with materials uniformly is a current urgent problem to be solved.
Chinese patent application No. CN 112410922A "a preparation method of aerogel-containing polyester fibers", wherein aerogel microspheres are mixed with first polyester resin powder to obtain uniform mixed powder, then uniformly mixed with second polyester resin slices for extrusion granulation, then uniformly mixed with third polyester resin slices for melt spinning, and in some embodiments, dispersing agents and antioxidants are added, but the problem of incompatibility in the direct mixing process of aerogel and plastic powder cannot be solved in practice. Chinese patent application No. CN 111534007A "multifunctional composite antiviral and antibacterial fiber master batch and preparation and application thereof" discloses that aerogel is adopted as various antiviral and antibacterial carriers, and then the aerogel is mixed with various fiber matrixes and spun by various spinning methods to prepare the antiviral and antibacterial fiber with heat-insulating effect. By loading the material in the aerogel structure, the dispersion properties when mixed with the fibrous matrix can be improved, but the insulating properties of the aerogel can be affected by the pore structure as a carrier.
Chinese patent application publication No. CN 110305340A "an aerogel composite plastic master batch, a preparation method and application thereof", wherein an aqueous resin and aerogel are mixed to obtain a mixed solution, and then the mixed solution is dispersed into a plastic matrix for re-granulation after spray drying and granulation, the resin in the heat insulation master batch cannot be removed before granulation, so that the basic performance of the master batch matrix is changed, and the efficiency is reduced due to repeated granulation. Chinese patent application No. CN111533990A "Heat insulation master batch and preparation method thereof", heat first polymer and nano pore material in the cylinder of plunger extruder to partial plasticize, start the plunger, extrude and granulate to get premix, then mix with second polymer and extrude and granulate with twin screw, but according to the patent, "first polymer particle located in Zhou Rongrong state can be coated on the surface of nano pore material", must ensure that there is always first polymer in molten state in the cylinder.
Therefore, there is a need for a method that can effectively mix aerogels with fibrous substrates and that can achieve continuous, efficient production.
Disclosure of Invention
In order to solve the technical problems that the density is not matched when the paste material and the resin matrix are used for preparing the aerogel master batch, the aerogel powder is unevenly dispersed in the master batch and the blanking is difficult in the granulating process, the first aspect of the application provides a high-dispersion aerogel master batch; the high-dispersion aerogel master batch is prepared by mixing aerogel paste material with a resin matrix.
In some preferred embodiments, the weight ratio of aerogel paste to resin matrix is 1: (0.5-10). The application adopts the aerogel paste material and the resin base material which are matched in density to optimize the mechanical property of the aerogel master batch.
In some preferred embodiments, the aerogel powder content in the aerogel masterbatch is 0.35 to 13wt% and the aerogel powder in the aerogel paste comprises 0.4 to 29.5wt% of the resin matrix.
In some preferred embodiments, the aerogel paste comprises, in parts by weight, 30 to 50 parts aerogel powder, 100 parts water, 1.2 to 5.3 parts surfactant, and 110 to 910 parts ceramic powder.
In some preferred embodiments, the aerogel powder is specifically hydrophobic aerogel powder, and the ceramic powder has an infrared reflection function, so that the heat preservation and insulation performance of the aerogel master batch is optimized.
In some preferred embodiments, the aerogel paste meets at least one of the following conditions:
(a) The density of the paste material is 0.9-1.3 g/cm 3
(b) The aerogel content is 4.2-15 wt%.
In some preferred embodiments, the aerogel powder satisfies at least one of the following conditions:
(a) The average grain diameter is 1-15 mu m;
(b) The tap density is 0.1-0.2 g/cm 3
(c) The thermal conductivity is less than 0.024W/(mK) at 25 ℃.
In some preferred embodiments, the ceramic powder comprises at least one of titanium dioxide, vanadium dioxide, zinc oxide, cesium oxide, tungsten trioxide, cesium tungstate, antimony tin oxide, yttrium oxide, tri-iron oxide, and tri-cobalt oxide.
Further preferably, the density of the ceramic powder is 4.1 to 7.2g/cm 3
According to the application, the preferable ceramic powder is adopted, so that on one hand, the density of the aerogel paste material can be improved to be matched with the density of the resin matrix, the technical problems of uneven mixing caused by mismatching of raw material density in the preparation process of actual master batch, inapplicability to blanking during granulation and uneven prepared master batch are solved, and on the other hand, the solid-phase heat conduction of a compatible system of the aerogel paste material and the resin matrix is reduced, the tendency of the reduction of the heat insulation performance of the master batch when the adding amount of the ceramic powder is increased is restrained, the formability of the aerogel master batch is improved, and meanwhile, the excellent heat insulation effect can be maintained, and compared with the heat insulation performance of the prepared aerogel master batch in the market, the heat insulation performance of the heat insulation material is better.
In some preferred embodiments, the resin matrix is a combination of one or more selected from polypropylene, polyethylene, polyamide, polyethylene terephthalate (PET), polybutylene terephthalate, polyvinyl chloride, polystyrene, ABS, polymethyl methacrylate, polyimide, polycarbonate.
In some preferred embodiments, there is a density differential of + -0.5 g/cm between the aerogel paste and the resin matrix 3 The density of the aerogel paste is 0.9-1.3 g/cm 3 The density of the resin matrix is 0.8-1.4 g/cm 3
Further preferably, the density difference between the aerogel paste and the resin matrix is + -0.1 g/cm 3
The second aspect of the application provides a preparation method of the high-dispersion aerogel master batch, which comprises the following specific preparation steps:
(a) Preparing aerogel paste;
(b) Mixing the aerogel paste material obtained in the step (a) with a resin matrix at 70-120 ℃ and 100-5000rpm for 10-180 min, and uniformly mixing and drying to obtain a mixture;
(c) Pouring the mixture into an extruder, extruding and granulating at 160-300 ℃ to obtain a high-dispersion aerogel master batch finished product.
Further preferably, the step (a) specifically comprises: the raw materials of the aerogel paste are put into a high-speed mixer and mixed for 5 to 40 minutes at the rotating speed of 1000 to 4500 rpm.
The second aspect of the application provides the application of the high-dispersion aerogel master batch in fibers, injection molding parts, films and plates.
Compared with the prior art, the application has the following beneficial effects:
(1) By adopting a density matching mechanism, aerogel paste materials and a resin matrix are mixed and granulated, the problem of dispersion caused by too low density of the aerogel is solved, materials can be mixed more uniformly, the problems of difficult discharging, dust pollution and the like in the process of preparing master batches are avoided, and the obtained aerogel master batches have good formability, heat preservation and heat insulation performance, and are simpler, more convenient and environment-friendly to operate.
(2) The paste material contains ceramic powder with infrared reflection function, so that the density of the paste material is improved, and meanwhile, the heat insulation performance of the aerogel paste material can be further maintained.
(3) The method can realize the preparation of multi-concentration multi-type heat preservation and insulation master batch, and form rich series products.
Drawings
FIG. 1 is an aerogel masterbatch prepared in example 1.
Detailed Description
The present application is illustrated by the following specific embodiments, but is not limited to the specific examples given below.
Example 1
The embodiment provides a high-dispersion aerogel fiber master batch, the high-dispersion aerogel master batch is made by mixing aerogel paste and resin matrix, the aerogel paste is waterborne aerogel paste, and the resin matrix is PET powder.
The preparation raw materials of the aqueous aerogel paste comprise the following components in parts by weight: 30 parts of aerogel powder, 100 parts of water, 2.13 parts of surfactant and 295 parts of ceramic powder.
The tap density of the aerogel powder is 0.1g/cm 3 The average particle diameter was 10. Mu.m, and the thermal conductivity was 0.018W/(mK).
The surfactant is specifically HY6170, the brand is Gojesi, and the surfactant is derived from Beijing Michael chemical technology Co.
The ceramic powder is specifically titanium dioxide, and the density of the titanium dioxide is 4.17g/cm 3
The PET resin is from China petrochemical and chemical fiber Limited liability company, and has the density of 1.4g/cm 3
The preparation method of the high-dispersion aerogel fiber master batch comprises the following steps:
(a) Mixing aerogel powder, water, titanium dioxide and surfactant in a high-speed mixer at 2500rpm for 8min to obtain a powder with density of 0.9g/cm 3 Aerogel paste with an aerogel powder content of 7.02 wt%;
(b) Putting the aerogel paste material obtained in the step (a) and the resin matrix into a high-speed mixer according to the weight ratio of 1:1, mixing at 1500rpm for 30min, and setting the mixing temperature to 70 ℃ to obtain a uniform mixture;
(c) Adding the mixture into a granulator, wherein the length-diameter ratio of a screw rod of the granulator is 40:1, setting the basic temperature to 275 ℃, extruding through a circular orifice die, cooling through a water tank, and pulling a brace to a granulator to cut into cylindrical particles with the length of 3mm plus or minus 1mm and the diameter of 2.5mm plus or minus 1.5mm, namely obtaining an aerogel master batch finished product; the aerogel content of the finished aerogel masterbatch was 3.98wt% (aerogel powder represents 7.02wt% of the resin matrix).
Heating the aerogel master batch obtained in the step (c) to 280 ℃ and casting into a plate with the thickness of 10cm multiplied by 2mm, wherein the heat conductivity coefficient of the tested plate is 0.046W/(m.K).
Example 2
The embodiment provides a high-dispersion aerogel fiber master batch, and the specific embodiment is the same as the embodiment 1; the difference is that the adding amount of the ceramic powder is 570 parts; the amount of the surfactant added was 3.5 parts.
The density of the aerogel paste obtained was 1.3g/cm 3 The content of aerogel powder is 4.26wt%.
The aerogel content of the obtained aerogel masterbatch was 2.3wt% (aerogel powder represents 4.26wt% of the resin matrix).
The aerogel master batch was heated to 280℃and cast into a 10cm 2mm sheet with a thermal conductivity of 0.053W/(m K).
Example 3
The embodiment provides a high-dispersion aerogel fiber master batch, and the specific embodiment is the same as the embodiment 1; the preparation method is characterized in that the preparation raw materials of the aqueous aerogel paste material comprise the following components in parts by weight: 50 parts of aerogel powder, 100 parts of water, 1.7 parts of surfactant and 190 parts of ceramic powder.
The tap density of the aerogel powder is 0.2g/cm 3 The average particle diameter was 10. Mu.m, and the thermal conductivity was 0.018W/(mK).
The ceramic powder is tungsten trioxide, and the density of the tungsten trioxide is 7.16g/cm 3
The density of the aerogel paste obtained was 0.9g/cm 3 The content of aerogel powder was 14.63wt%.
The aerogel content of the obtained aerogel masterbatch was 8.57wt% (aerogel powder accounted for 14.63wt% of the resin matrix).
The aerogel master batch was heated to 280℃and cast into a 10cm 2mm sheet with a thermal conductivity of 0.035W/(m K).
Example 4
The embodiment provides a high-dispersion aerogel fiber master batch, and the specific implementation mode is the same as that of the embodiment 3; the difference is that the adding amount of the ceramic powder is 375 parts; the amount of the surfactant added was 2.63 parts.
The density of the aerogel paste obtained was 1.3g/cm 3 The content of aerogel powder is 9.48wt%.
The aerogel content of the obtained aerogel master batch was 5.23wt% of aerogel (aerogel powder was 9.48wt% of the resin matrix).
The aerogel master batch was heated to 280℃and cast into a 10cm 2mm sheet with a thermal conductivity of 0.04W/(mK).
The parts by weight of water used in examples 5-12 were 100 parts, and the other raw materials, the paste density, the paste aerogel content and the related information of the master batch are shown in Table 1.
TABLE 1
Comparative example 1
This comparative example provides a highly dispersed aerogel fiber masterbatch, the embodiment being the same as example 1; the difference is that the addition amount of the ceramic powder is 0 part; the amount of the surfactant added was 0.65 part.
The density of the aerogel paste obtained was 0.33g/cm 3 The content of aerogel powder is 22.96wt%.
The aerogel content of the obtained aerogel masterbatch was 18.6wt% (aerogel powder accounted for 22.96wt% of the resin matrix).
The aerogel master batch was heated to 280℃and cast into a 10cm 2mm sheet with a thermal conductivity of 0.085W/(m K).
Comparative example 2
This comparative example provides a highly dispersed aerogel fiber masterbatch, the embodiment being the same as example 1; except that the aerogel paste was replaced with aerogel powder within the scope of the present application.
The tap density of the aerogel powder is 0.2g/cm 3
The aerogel theoretical content of the obtained aerogel master batch is 50wt%, the bleaching powder is serious in the actual mixing process, the mixing weight ratio of the aerogel powder to the resin matrix is far lower than 1:1 through multiple tests, and the problems of difficult discharging, difficult smooth extrusion and the like still exist in granulating, so that the master batch is nonuniform.
The aerogel master batch was heated to 280℃and cast into a 10cm 2mm sheet with a thermal conductivity of 0.12W/(mK).
Comparative example 3
This comparative example provides a highly dispersed aerogel fiber masterbatch, the embodiment being the same as example 9; the difference is that the addition amount of the aerogel powder is 60 parts; the amount of the surfactant added was 1.35 parts.
The density of the aerogel paste obtained was 0.65g/cm 3 The content of aerogel powder is 22.11wt%.
The aerogel content of the obtained aerogel masterbatch was 14.74wt% (aerogel powder accounted for 44.22wt% of the resin matrix).
The aerogel master batch was heated to 280℃and cast into a 10cm 2mm plate with a thermal conductivity of 0.043W/(m K).
Comparative example 4
This comparative example provides a highly dispersed aerogel fiber masterbatch, the embodiment being the same as example 11; the difference is that the addition amount of the aerogel powder is 20 parts; the amount of the surfactant added was 5.15 parts.
The density of the aerogel paste obtained was 1.99g/cm 3 The content of aerogel powder is 1.93wt%.
The aerogel content of the obtained aerogel masterbatch was 1.29wt% (aerogel powder accounted for 3.86wt% of the resin matrix).
The aerogel master batch was heated to 280℃and cast into a 10cm 2mm panel, the thermal conductivity of the test panel being 0.078W/(m K), higher than that of example 11.
Compared with example 9, the thermal conductivity of the plate of comparative example 3 is higher, because the density of the paste is too low due to the addition of too much aerogel powder, the adaptation effect with the resin matrix is poor, uneven dispersion occurs when the paste is mixed with the resin matrix, and the masterbatch is uneven in texture, thereby affecting the performance. In addition, although the thermal conductivity of comparative example 3 was lower than that of some examples, 60 parts of aerogel powder was added in comparative example 3, the content of aerogel powder in the paste was 22.11wt% which was far higher than that of the other examples, indicating that the effect of lowering the thermal conductivity could not be obtained by increasing the added amount of aerogel powder at one time, indicating that the added amount of aerogel powder defined in the present application was appropriate.
Compared with the embodiment 1, the comparative example 1 is free from adding titanium dioxide to prepare a paste with lower density, and when the paste is mixed with PET powder, the density difference is large, so that the mixing effect of aerogel powder and a plastic matrix is not ideal, layering phenomenon occurs, the blanking is difficult, the uniformity of the produced aerogel master batch is poor, the heat conductivity coefficient of the aerogel master batch is influenced, and the heat preservation performance of the aerogel master batch is poor. In comparative example 2, aerogel powder and PET powder are directly added for mixing, and the density difference between the aerogel powder and the density of the plastic matrix is very poor, so that the mixing effect of the aerogel powder and the plastic matrix is very poor, the aerogel powder floats on the upper part of the mixture, layering phenomenon occurs, the mixture is difficult to discharge during granulation, and the uniformity of the produced aerogel fiber master batch is very poor. The aerogel paste prepared in comparative example 3 and comparative example 4 respectively use more and less aerogel powder, the density of the prepared aerogel paste is lower and higher, the prepared aerogel paste is mixed with a resin matrix, the prepared aerogel paste is unevenly dispersed, and the prepared aerogel paste has uneven texture, so that the performance is affected.
According to the high-dispersion aerogel fiber master batch, based on excellent granulating formability of a plastic matrix, aerogel is added to enhance heat insulation performance of the high-dispersion aerogel fiber master batch, and a density-matched mixed system is designed, so that the prepared master batch not only has good strength and toughness, but also has high heat insulation performance. In comparative example 1, a low-density paste material was mixed with a resin matrix, and the density was greatly different, so that the mixing was not uniform during actual mixing, the discharging was difficult during granulation, and the master batch was not uniform. It is stated that the density of the paste and the plastic matrix must be adapted within a certain range in order to achieve good granulation. Comparative example 2 the aerogel powder within the limits of the present application was mixed with the resin matrix to be granulated, and the blanking was difficult, so that a high density paste was required to be prepared. Comparative example 3 the aerogel powder used to prepare the paste was added in an amount above the upper limit defined by the present application, and although the aerogel content in the obtained paste was up to 14.74% by weight, the thermal conductivity of the prepared sheet was 0.043W/(m.k), which was higher than that of comparative example 9 (0.03W/(m.k)), indicating that on the basis of the paste formulation defined by the present application, the aerogel powder addition was continued to be increased although the aerogel content in the paste could be increased and the corresponding effect of lowering the thermal conductivity could not be obtained, indicating that the aerogel powder addition defined in the present application was suitable. Comparative example 4 the aerogel powder used to prepare the paste was added in an amount falling outside the lower limit defined by the present application, the density of the prepared paste was increased, the aerogel content was decreased, the dispersibility of the aerogel in the resin matrix was decreased due to the increase in density, the performance was affected, and the decrease in the aerogel content also resulted in an increase in the thermal conductivity. In addition, compared with a resin matrix (such as PET master batch, the heat conductivity coefficient at room temperature is about 0.2W/(m.K)), the aerogel master batch disclosed by the application has better heat insulation performance than a pure resin master batch, and has high practical application value.

Claims (8)

1. The high-dispersion aerogel master batch is characterized by being prepared by mixing aerogel paste and a resin matrix;
the weight ratio of aerogel paste to resin matrix is 1: (0.5-10);
the content of aerogel powder in the aerogel master batch is 0.35-13wt%;
aerogel powder in the aerogel master batch accounts for 0.4-29.5wt% of the resin matrix;
according to parts by weight, the aerogel paste comprises 30-50 parts of aerogel powder, 100 parts of water, 1.2-5.3 parts of surfactant and 110-910 parts of ceramic powder;
the aerogel paste material is matched with the density of the resin matrix, and the density difference is +/-0.5 g/cm 3 Within the range, the density of the aerogel paste is 0.9-1.3 g/cm 3
2. The high dispersion aerogel masterbatch according to claim 1, characterized in that: the aerogel powder is hydrophobic aerogel powder, and the ceramic powder has an infrared reflection function.
3. The high dispersion aerogel masterbatch according to any one of claims 1-2, characterized in that: the aerogel paste satisfies the following conditions:
the aerogel paste contains 4.2-15wt% of aerogel powder.
4. The high dispersion aerogel masterbatch according to claim 1, wherein the ceramic powder comprises at least one of titanium dioxide, vanadium dioxide, zinc oxide, cesium oxide, tungsten trioxide, cesium tungstate, antimony tin oxide, yttrium oxide, tri-iron oxide, and tri-cobalt oxide.
5. The high dispersion aerogel masterbatch according to claim 1, characterized in that the density of the ceramic powder is 4.1-7.2 g/cm 3
6. The high dispersion aerogel masterbatch according to claim 1, characterized in that the resin matrix is a combination of one or more selected from polypropylene, polyethylene, polyamide, polyethylene terephthalate, polybutylene terephthalate, polyvinyl chloride, polystyrene, ABS, polymethyl methacrylate, polyimide, polycarbonate.
7. A method of preparing a highly dispersed aerogel masterbatch according to any one of claims 1-6 characterized by the specific preparation steps comprising:
(a) Preparing aerogel paste;
(b) Mixing the aerogel paste material obtained in the step (a) and the resin matrix at 70-120 ℃ and 100-5000rpm for 10-180 min, and uniformly mixing and drying to obtain a mixture;
(c) Pouring the mixture into an extruder, extruding and granulating at 160-300 ℃ to obtain a high-dispersion aerogel master batch finished product.
8. Use of the high dispersion aerogel masterbatch according to any of claims 1-6 in fibers, injection molded parts, films, sheets.
CN202210552954.8A 2022-05-19 2022-05-19 High-dispersion aerogel master batch and preparation method and application thereof Active CN115216124B (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101143981A (en) * 2007-09-14 2008-03-19 哈尔滨工业大学 Powder coating containing aerogel particles and preparing method thereof
CN104496399A (en) * 2014-12-15 2015-04-08 苏州同玄新材料有限公司 Aerogel building heat preservation and thermal insulation composite material and preparation method thereof
CN106633691A (en) * 2016-12-01 2017-05-10 深圳中凝科技有限公司 Aerogel PET (polyethylene terephthalate) master batch and manufacturing technique thereof
CN106757513A (en) * 2016-12-01 2017-05-31 深圳中凝科技有限公司 Aeroge composite fibre and its manufacture craft
CN112410922A (en) * 2020-11-20 2021-02-26 素湃科技(上海)有限公司 Preparation method of aerogel-containing polyester fiber

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101143981A (en) * 2007-09-14 2008-03-19 哈尔滨工业大学 Powder coating containing aerogel particles and preparing method thereof
CN104496399A (en) * 2014-12-15 2015-04-08 苏州同玄新材料有限公司 Aerogel building heat preservation and thermal insulation composite material and preparation method thereof
CN106633691A (en) * 2016-12-01 2017-05-10 深圳中凝科技有限公司 Aerogel PET (polyethylene terephthalate) master batch and manufacturing technique thereof
CN106757513A (en) * 2016-12-01 2017-05-31 深圳中凝科技有限公司 Aeroge composite fibre and its manufacture craft
CN112410922A (en) * 2020-11-20 2021-02-26 素湃科技(上海)有限公司 Preparation method of aerogel-containing polyester fiber

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