CN111136851B - High-strength corrosion-resistant product and preparation method thereof - Google Patents
High-strength corrosion-resistant product and preparation method thereof Download PDFInfo
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- CN111136851B CN111136851B CN201911413300.1A CN201911413300A CN111136851B CN 111136851 B CN111136851 B CN 111136851B CN 201911413300 A CN201911413300 A CN 201911413300A CN 111136851 B CN111136851 B CN 111136851B
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/02—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles
- B29C44/12—Incorporating or moulding on preformed parts, e.g. inserts or reinforcements
- B29C44/1266—Incorporating or moulding on preformed parts, e.g. inserts or reinforcements the preformed part being completely encapsulated, e.g. for packaging purposes or as reinforcement
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
- B32B15/09—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising polyesters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0066—Use of inorganic compounding ingredients
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/009—Use of pretreated compounding ingredients
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
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- E—FIXED CONSTRUCTIONS
- E03—WATER SUPPLY; SEWERAGE
- E03F—SEWERS; CESSPOOLS
- E03F5/00—Sewerage structures
- E03F5/04—Gullies inlets, road sinks, floor drains with or without odour seals or sediment traps
- E03F5/0407—Floor drains for indoor use
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/558—Impact strength, toughness
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/714—Inert, i.e. inert to chemical degradation, corrosion
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2205/00—Foams characterised by their properties
- C08J2205/04—Foams characterised by their properties characterised by the foam pores
- C08J2205/044—Micropores, i.e. average diameter being between 0,1 micrometer and 0,1 millimeter
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2367/06—Unsaturated polyesters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2423/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2423/04—Homopolymers or copolymers of ethene
- C08J2423/06—Polyethene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2425/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
- C08J2425/02—Homopolymers or copolymers of hydrocarbons
- C08J2425/04—Homopolymers or copolymers of styrene
- C08J2425/06—Polystyrene
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- C—CHEMISTRY; METALLURGY
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2433/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2433/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
- C08J2433/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C08J2433/10—Homopolymers or copolymers of methacrylic acid esters
- C08J2433/12—Homopolymers or copolymers of methyl methacrylate
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/06—Pretreated ingredients and ingredients covered by the main groups C08K3/00 - C08K7/00
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2206—Oxides; Hydroxides of metals of calcium, strontium or barium
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2217—Oxides; Hydroxides of metals of magnesium
- C08K2003/222—Magnesia, i.e. magnesium oxide
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
- C08K2003/3045—Sulfates
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/14—Glass
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
- C08K7/26—Silicon- containing compounds
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
- C08K9/06—Ingredients treated with organic substances with silicon-containing compounds
Abstract
The invention discloses a preparation method of a high-strength corrosion-resistant product, wherein the high-strength corrosion-resistant product comprises thermosetting resin and metal coated in the thermosetting resin; the thermosetting resin has compact surface and foam pores inside, and the size of the foam pores is gradually reduced from the inner surface contacting with the metal surface to the outer surface of the resin from inside to outside. The product of the invention has strong pressure resistance and corrosion resistance and is easy to clean.
Description
Technical Field
The invention relates to a high-strength corrosion-resistant product and a preparation method thereof.
Background
The bathroom floor drain material is mainly made of metal materials such as stainless steel, copper-zinc alloy and the like and plastic materials, wherein the common plastic (PP/ABS/PVC) floor drain has poor texture, low density, and no high temperature resistance or scratch resistance; stainless steel floor drains and electroplated floor drains are not resistant to acid corrosion and are easy to rust; the surface treatment process (spraying and the like) of the metal material is easy to fall off.
To above problem, the body floor drain is produced by:
1. high performance thermoplastic materials: polyphenylene Sulfide (PPS), Polyoxymethylene (POM), tetramethylene terephthalate (PBT), and the like; the high-performance thermoplastic materials have excellent performance, but have the defects of poor texture, strong plastic texture, general impact resistance, high energy consumption and the like;
2. special ceramic floor drain: such as zirconia ceramic floor drains; however, they have low strength, poor impact resistance, insufficient stain resistance, large energy consumption, and the like.
3. Other thermosetting materials: after injection molding or die pressing, the brittleness is high, the strength is low, the stain resistance is poor, the appearance quality is poor and the like.
Disclosure of Invention
The invention mainly aims to provide a high-strength (compression-resistant) corrosion-resistant product.
The technical scheme adopted by the invention for solving the technical problem is as follows:
a preparation method of a high-strength corrosion-resistant product comprises the following steps:
1) processing a metal sample into a desired shape;
2) preparing a resin raw material into to-be-foamed bulk composite resin, forming a to-be-foamed bulk resin-metal-to-be-foamed bulk resin sandwich structure, and putting the to-be-foamed bulk resin sandwich structure into a mold; wherein the resin raw material comprises unsaturated polyester and a foaming agent, and the foaming temperature of the foaming agent is higher than the lowest thermosetting molding temperature of the unsaturated polyester;
3) the mould is closed and heated to cure and form the composite resin, and the metal is heated in the process by adopting a mode including electromagnetic heating, wherein the heating temperature of the mould is lower than the heating temperature of the metal and is equal to or higher than the lowest thermosetting forming temperature of the unsaturated polyester; the heating temperature of the metal is equal to or greater than the foaming temperature of the foaming agent.
Preferably, the foaming temperature of the blowing agent is higher than the lowest thermosetting molding temperature of the unsaturated polyester and lower than the highest thermosetting molding temperature of the unsaturated polyester.
Preferably, the heating temperature of the metal is 0.1 to 10 ℃ higher than the foaming temperature of the foaming agent.
In the invention, the high-strength corrosion-resistant product comprises at least one of a floor drain, a basin, a storage rack, a urinal and the like.
Preferably, the metal comprises at least one of iron or stainless steel.
Preferably, the resin raw materials comprise, by mass:
30% -50% of unsaturated polyester; 20-40% of reinforcing fiber, and foaming agent: 0.5 to 4 percent;
gas-phase white carbon black: 0.5 to 1.5 percent; fluorine-containing compound: 1% -8%; thickening agent: 0.05% -0.1%;
1% -8% of low shrinkage agent: initiator: 0.5% -3%; 1.5 to 3 percent of other auxiliary agents;
the balance of inorganic modified filler;
wherein, the unsaturated polyester comprises one or the combination of ortho-benzene type, meta-benzene type, bisphenol A type and neopentyl glycol type;
the inorganic modified filler comprises at least one of calcium carbonate, barium sulfate, hydrated alumina and nano ceramic powder, and the particle size is 200-800 meshes;
the reinforced fiber comprises at least one of glass fiber/carbon fiber/aramid fiber, and the thickness of the reinforced fiber is 4-10 mm;
the foaming agent is at least one of core-shell polymer, Azodicarbonamide (AC) and supercritical gas; the supercritical gas can be carbon dioxide or nitrogen.
Fumed silica with particle size of 5-800 nm;
fluorine-containing compound: comprises at least one of methacrylic acid fluorine-containing ester and fluorosilane;
in a preferred embodiment of the present invention,
the thickener comprises at least one of calcium hydroxide and magnesium oxide;
the low shrinkage agent comprises at least one of PMMA (polymethyl methacrylate)/PE (polyethylene)/PS (polystyrene);
the initiator is peroxide;
other auxiliary agents comprise at least one of polymerization inhibitor, internal release agent, colorant and the like;
the inorganic filler comprises at least one of calcium carbonate, barium sulfate, hydrated alumina and nano ceramic powder.
Preferably, the metal is fixed in a mold, wherein the mold upper/lower mold has an electromagnetic heating device that can perform space heating of the metal insert module embedded in the resin.
Preferably, the mold is evacuated and maintained for 50s to 300s while heating the metal and the resin.
Preferably, in the step 2), the resin is prepared into the to-be-foamed dough-shaped composite resin, and the to-be-foamed dough-shaped resin sandwich structure is formed and put into a mould.
Preferably, the preparation method of the dough-like composite resin to be foamed comprises the following steps:
(1) mixing and kneading: uniformly mixing and stirring unsaturated polyester for 4-6h, adding raw materials including filler, hydrophobic fumed silica, initiator/polymerization inhibitor and glass fiber, mixing and kneading for 5-15min, controlling the temperature to be less than or equal to 30 ℃, and preparing uniform bulk resin;
(2) foaming and kneading: and (3) immediately and slowly adding a foaming agent and other resin components into the bulk resin, and further kneading the mixture for 3-5min by using a kneader to prepare the bulk composite resin to be foamed.
Preferably, the foaming agent is selected from core-shell polymers and is subjected to the following surface treatment: spraying silane coupling agent on the surface of the core-shell polymer, stirring uniformly, quantitatively soaking the treated core-shell polymer into a polyester system, uniformly dispersing by adopting ultrasonic waves, and stirring for 10-20min, wherein the temperature is controlled to be less than or equal to 30 ℃.
The conventional heating method of thermosetting resin is to carry out heat transfer molding from outside to inside, and aims at solving the problems that small molecules are separated out to release gas in the curing process of an upper die and the problems of poor surface quality, serious gas mark, pollution resistance, poor corrosion resistance and the like easily occur when the material is subjected to the traditional heating treatment mode; meanwhile, the invention adopts a microporous foaming structure to realize a double sandwich structure, so that the cost is saved, the density is reduced, and the toughness and the shock resistance of the material can be improved. The principle is as follows:
1. micro-nano pore foaming structure-toughening:
the microporous structure can produce a large amount of silver veins when the product receives the impact, and a large amount of energy can be absorbed to this process, slows down the injury that the impact brought: when the micropores are uniformly distributed in the material, the stress field is not uniform, the force at the impact point can be consumed to other micropore structures through the micro-nano pore structure, a large amount of silver lines are gradually generated, the stress diffusion is stopped, destructive cracks or cracking cannot be generated, and the macroscopic expression means that when the material is impacted by external force or high and low temperature internal stress, the material can be self-digested and buffered, the toughness is enhanced, the phenomena of product cracking and the like cannot be generated; the core-shell polymer is preferably selected, so that the phenomenon that AC or supercritical gas forms nucleation points on the surface of the glass fiber to form defects is avoided;
2. double "sandwich" structure-toughening/cost/density reduction:
embedded heating metal structure, inside and outside heating unit simultaneous working impels inside foaming earlier shaping, surface crust, constructs the foam sandwich structure: the curing temperature of the upper/lower die is lower than the foaming temperature, the upper/lower surface is not foamed, the upper/lower surface is subjected to skinning and shaping after being slowly leveled, the surface skinning is compact and uniform, the interior is foamed from inside to outside, the size of the foam hole is gradually reduced from inside to outside to form a sandwich structure, meanwhile, a metal structure is embedded, thermosetting modified resin is coated outside the foam hole, and the overall structure of the more stable sandwich structure is more stable;
3. surface skinning-stain/corrosion/gas mark improvement:
the temperature of the upper die and the lower die is lower than the expansion temperature (namely the foaming temperature) of the foaming material, the bulk resin has strong fluidity in the die pressing process, is flatly spread under the pressure of the die and is cured and molded, the surface is compact and uniform, and the defects of serious pressure marks and the like of the traditional die are obviously improved; meanwhile, because the thickness of the product is larger, the inner curing speed is slow or the inner cracking is generated due to no curing when the upper die and the lower die are heated, and the curing process can effectively solve the problem;
the product of the invention has excellent corrosion resistance, high strength, good surface quality, low density and low cost; the strength and impact resistance of the product can be better improved by adopting the core-shell polymer microcellular foaming structure, the strength and bearing capacity of the product can be obviously improved by adopting a metal embedded structure heating mode, and the surface defect, the product quality and the corrosion resistance and corrosion resistance of the product can be improved by the preparation process.
Drawings
The invention is further illustrated by the following figures and examples.
FIG. 1 is a schematic diagram of the principles of the present invention;
FIG. 2 is a comparative drawing of the floor drain product of example 1 (left) and the existing floor drain product (right)
Detailed Description
Example 1
Taking a floor drain product as an example, the technical scheme of the invention is as follows:
the basic scheme comprises the following formula:
40% of unsaturated polyester: AROPOL MR14029 resin
The balance of inorganic modified filler: barium sulfate
30% of glass fiber: thai glass fiber Limited, glass fiber length 5mm-8mm
Core-shell polymer blowing agent: 2%: PG16 foaming agent, Beijing Shanghai brocade science and technology Limited
Gas-phase white carbon black: 1%: hydrophobic fumed silica of Yingchuangdegussa
Fluorine-containing methacrylic acid ester: 5%: aldrich Co of USA
Thickening agent: 0.1% magnesium oxide
Low shrinkage agent: PMMA/PE/PS, PMMA was used in this example at a level of 5%
Initiator: TBPB tert-butyl peroxybenzoate, 1.5%; purchased from Akema, TBPO peroxy-2-ethylhexoate, 1.5%, and purchased from Aksu
1.5 percent of other auxiliary agents
A heat-conducting metal structure: stainless steel, iron, etc., and is formed by stamping or casting, and the thickness is 0.5mm
The preparation method comprises the following steps:
1) surface treatment of the core-shell polymer: spraying a silane coupling agent on the surface of the core-shell polymer, quantitatively soaking the treated core-shell polymer into an unsaturated polyester system after uniformly stirring, uniformly dispersing and stirring for 15min by adopting ultrasonic waves, and controlling the temperature to be less than or equal to 30 ℃;
2) and (3) surface treatment of fumed silica: adding fumed silica into deionized water, stirring uniformly, adding 10-20% of silane coupling agent, heating, fully performing reflux reaction, and baking in an oven at 100 ℃ to prepare hydrophobic modified fumed silica;
3) mixing and kneading: uniformly mixing and stirring unsaturated polyester for 5 hours, adding filler (the water content is less than or equal to 0.1 percent), hydrophobic fumed silica, initiator/polymerization inhibitor, glass fiber (the water content is less than or equal to 0.1 percent) and the like, mixing and kneading for 10 minutes, controlling the temperature to be less than or equal to 30 ℃, and preparing uniform bulk resin;
4) foaming and kneading: slowly adding the core-shell polymer and resin system dispersed in the step 1) into the bulk resin (uniformly adding), further kneading for 4min by adopting a kneader to finish preparing the bulk composite resin to be foamed, and storing at 25 ℃;
5) forming a metal sample sheet: punching and forming a metal sample to prepare an embedded structure module;
6) surface treatment of the metal embedded module: carrying out surface roughening treatment on the metal embedded structure module by adopting a sand blasting/chemical etching process, then carrying out ultrasonic cleaning, and carrying out pretreatment in a high-temperature oven for more than 1 h;
7) compression molding: the mould preheats, will wait to foam bulk resin, metal embedding module, wait to foam bulk resin and put into the mould fixedly (sandwich structure) in proper order, and wherein metal embedding module can be fixed to in the mould, and the upper/lower mould of mould has electromagnetic heating device, can separate empty heating to the metal embedding module of embedding into in the resin. Then, the mould and the metal are heated to the thermosetting molding temperature of the resin, and then the metal temperature is independently raised by 5-20 ℃ by utilizing an electromagnetic heating device. Exhausting and maintaining the pressure for 50-300 s;
8) and (3) flash treatment: taking out and cooling the product and then carrying out flash treatment.
Results
The floor drain has good corrosion resistance/good hydrophobicity, is not easy to be corroded and polluted by the external environment, has high strength, good impact resistance and easy cleaning of drainage, has great product performance advantage compared with the traditional stainless steel floor drain, adopts a mould pressing or injection molding process, has strong designability of product structure and designable appearance color, and has the performance which can not be achieved by stainless steel or metal floor drains;
example 2
Taking a urinal product as an example, the technical scheme of the invention is as follows:
the basic scheme comprises the following formula:
45% of unsaturated polyester: AROPOL MR14029 resin
Inorganic modified filler: the balance of barium sulfate%
18% of glass fiber: 4-6mm of Taian glass fiber Co
Core-shell polymer blowing agent: 0.5%: PG18 foaming agent of Beijing Shanghai brocade science and technology Limited
Gas-phase white carbon black: 1.5%: hydrophobic fumed silica of Yingchuangdegussa
Fluorine-containing methacrylic acid ester: 3.5%: aldrich Co of USA
Thickening agent: 0.08% of calcium hydroxide and magnesium oxide
Low shrinkage agent: PMMA
Initiator: TBPB tert-butyl peroxybenzoate, 1.5% from Achima, TBPO tert-butyl peroxy-2-ethylhexanoate, 1.5% from Acksu;
1.5 percent of other auxiliary agents
A heat-conducting metal structure: stamping and molding stainless steel with the thickness of 1.5mm
The preparation method comprises the following steps:
1) surface treatment of the core-shell polymer: spraying a silane coupling agent on the surface of the core-shell polymer, quantitatively soaking the treated core-shell polymer into an unsaturated polyester system after uniformly stirring, uniformly dispersing and stirring for 15min by adopting ultrasonic waves, and controlling the temperature to be less than or equal to 30 ℃;
2) and (3) surface treatment of fumed silica: adding fumed silica into deionized water, stirring uniformly, adding 10-20% of silane coupling agent, heating, carrying out reflux reaction, and baking in an oven at 100 ℃ to prepare hydrophobic modified fumed silica;
3) mixing and kneading: uniformly mixing and stirring unsaturated polyester for 5 hours, adding filler (the water content is less than or equal to 0.1 percent), hydrophobic fumed silica, initiator/polymerization inhibitor, glass fiber (the water content is less than or equal to 0.1 percent) and the like, mixing and kneading for 10 minutes, controlling the temperature to be less than or equal to 30 ℃, and preparing uniform bulk resin;
4) foaming and kneading: slowly adding the core-shell polymer and resin system dispersed in the step 1 into the bulk resin (uniformly adding), further kneading for 4min by adopting a kneader to finish preparing the bulk composite resin to be foamed, and storing at 25 ℃;
5) forming a metal sample sheet: punching a metal sample to prepare an embedded structure module, and processing a welding support structure for installation on a wall surface;
6) surface treatment of the metal embedded module: carrying out surface roughening treatment on the metal embedded structure module by adopting a sand blasting/chemical etching process, then carrying out ultrasonic cleaning, and carrying out pretreatment in a high-temperature oven for more than 1 h;
7) compression molding: the mould preheats, will wait to foam bulk resin, metal embedding module, wait to foam bulk resin and put into the mould fixedly (sandwich structure) in proper order, wherein metal embedding module can be fixed to in the mould, wherein the mould is gone up/lower mould and is had electromagnetic heating device, can separate empty heating to the metal embedding module of embedding into in the resin. Then, the mould and the metal are heated to the thermosetting molding temperature of the resin, and then the metal temperature is independently raised by 5-20 ℃ by utilizing an electromagnetic heating device. Exhausting and maintaining the pressure for 50-300 s;
8) and (3) flash treatment: taking out and cooling the product and then carrying out flash treatment.
The urinal made of the material has the advantages of low product density, high impact resistance, difficult crushing, convenient transportation, good hydrophobicity, easy cleaning, good corrosion resistance, difficult corrosion and rusting, and obvious comprehensive performance advantage compared with common ceramic urinals and stainless steel urinals; simultaneously, compared with stainless steel urinals and ceramic urinals, the material has a series of advantages of better dimensional stability, strong designability of color, low production energy consumption and the like.
Claims (10)
1. A preparation method of a high-strength corrosion-resistant product comprises the following steps:
1) processing a metal sample into a desired shape;
2) preparing a resin raw material into to-be-foamed bulk composite resin, forming a to-be-foamed bulk resin-metal-to-be-foamed bulk resin sandwich structure, and putting the to-be-foamed bulk resin sandwich structure into a mold; wherein the resin raw material comprises unsaturated polyester and a foaming agent, and the foaming temperature of the foaming agent is higher than the lowest thermosetting molding temperature of the unsaturated polyester;
3) the mould is closed and heated to cure and form the composite resin, and the metal is heated in the process by adopting a mode including electromagnetic heating, wherein the heating temperature of the mould is lower than the heating temperature of the metal and is equal to or higher than the lowest thermosetting forming temperature of the unsaturated polyester; the heating temperature of the metal is equal to or greater than the foaming temperature of the foaming agent; the temperature of the upper die and the lower die is lower than the foaming temperature of the foaming material.
2. The method of claim 1, wherein the step of forming a high strength corrosion resistant article comprises: the foaming temperature of the foaming agent is higher than the lowest thermosetting molding temperature of the unsaturated polyester and lower than the highest thermosetting molding temperature of the unsaturated polyester.
3. The method of claim 1, wherein the step of forming a high strength corrosion resistant article comprises: the heating temperature of the metal is 0.1-10 ℃ higher than the foaming temperature of the foaming agent.
4. The method of claim 1, wherein the step of forming a high strength corrosion resistant article comprises: the heating temperature of the metal is 5-20 ℃ higher than that of the mould.
5. The method of claim 1, wherein the method further comprises: the resin raw materials comprise the following components in percentage by mass:
unsaturated polyester: 30% -50%; reinforcing fibers: 20% -40%, foaming agent: 0.5 to 4 percent;
gas-phase white carbon black: 0.5 to 1.5 percent; fluorine-containing compound: 1% -8%; thickening agent: 0.05% -0.1%;
low shrinkage agent: 1% -10%; initiator: 0.5 to 3 percent; other auxiliary agents: 1.5% -3%;
inorganic modified filler: the balance;
wherein the unsaturated polyester comprises at least one of ortho-benzene type, meta-benzene type, bisphenol A type and neopentyl glycol type;
the inorganic modified filler comprises at least one of calcium carbonate, barium sulfate, hydrated alumina and nano ceramic powder, and the particle size is 200-800 meshes;
the reinforced fiber comprises at least one of glass fiber/carbon fiber/aramid fiber, and the length of the reinforced fiber is 4-10 mm;
the foaming agent is at least one of core-shell polymer, azodicarbonamide and supercritical gas;
fumed silica with particle size of 5-800 nm;
fluorine-containing compound: comprises at least one of methacrylic acid fluorine-containing ester and fluorosilane.
6. The method of claim 5, wherein the method further comprises:
the thickener comprises at least one of calcium hydroxide and magnesium oxide;
the low shrinkage agent comprises at least one of PMMA/PE/PS;
the initiator is at least one of peroxide, styrene, methyl methacrylate and diallyl phthalate;
the other auxiliary agents comprise at least one of polymerization inhibitor, internal release agent and colorant;
the inorganic filler comprises at least one of calcium carbonate, barium sulfate, hydrated alumina and nano ceramic powder.
7. The method of claim 1, wherein the method further comprises: the metal is fixed in a mold, wherein the upper/lower mold of the mold has an electromagnetic heating device capable of space-heating a metal insert module embedded in the resin.
8. The method of claim 1, wherein the method further comprises: when the metal and the resin are heated, the mold is exhausted for 0.5s-3s, and then the mold is closed and the pressure is maintained for 50s-300 s.
9. The method of claim 1, wherein the method further comprises:
the preparation method of the to-be-foamed bulk composite resin comprises the following steps of:
(1) mixing and kneading: uniformly mixing and stirring a polyester system for 4-6h, adding raw materials including a filler, hydrophobic fumed silica, an initiator/polymerization inhibitor and glass fibers, mixing and kneading for 5-15min, controlling the temperature to be less than or equal to 30 ℃, and preparing uniform bulk resin;
(2) foaming and kneading: and (3) immediately and slowly adding a foaming agent and other resin components into the bulk resin, and further kneading the mixture for 3-5min by using a kneader to prepare the bulk composite resin to be foamed.
10. The method of claim 5, wherein the method further comprises: the foaming agent adopts core-shell polymer and is treated by the following steps: spraying silane coupling agent on the surface of the core-shell polymer, stirring uniformly, quantitatively soaking the treated core-shell polymer into a polyester system, uniformly dispersing by adopting ultrasonic waves, and stirring for 10-20min, wherein the temperature is controlled to be less than or equal to 30 ℃.
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CN112976459B (en) * | 2021-02-05 | 2022-09-23 | 广州辰东新材料有限公司 | Micro-foaming nano injection molding method for preparing low dielectric resin metal complex |
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