WO2013177850A1 - 具有激光直接成型功能的树脂组合物、其制备方法以及该树脂组合物的应用 - Google Patents

具有激光直接成型功能的树脂组合物、其制备方法以及该树脂组合物的应用 Download PDF

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WO2013177850A1
WO2013177850A1 PCT/CN2012/078643 CN2012078643W WO2013177850A1 WO 2013177850 A1 WO2013177850 A1 WO 2013177850A1 CN 2012078643 W CN2012078643 W CN 2012078643W WO 2013177850 A1 WO2013177850 A1 WO 2013177850A1
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resin composition
composition according
laser
resin
additives
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PCT/CN2012/078643
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English (en)
French (fr)
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严峡
蔡彤旻
宁凯军
姜苏俊
蒋智强
宁方林
叶南飚
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金发科技股份有限公司
上海金发科技发展有限公司
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Publication of WO2013177850A1 publication Critical patent/WO2013177850A1/zh

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/08Polyethers derived from hydroxy compounds or from their metallic derivatives
    • C08L71/10Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
    • C08L71/12Polyphenylene oxides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/02Polyamides derived from omega-amino carboxylic acids or from lactams thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/06Polyamides derived from polyamines and polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L79/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
    • C08L79/04Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
    • C08L79/08Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2650/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G2650/28Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
    • C08G2650/38Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group
    • C08G2650/40Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group containing ketone groups, e.g. polyarylethylketones, PEEK or PEK
    • 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
    • C08K2003/2217Oxides; Hydroxides of metals of magnesium
    • 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
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/02Fibres or whiskers
    • C08K7/04Fibres or whiskers inorganic
    • C08K7/14Glass

Definitions

  • Resin composition having laser direct structuring function, preparation method thereof, and application of the resin composition
  • the present invention relates to a resin composition, and more particularly to a thermally conductive resin composition having a Laser Direct Structuring function, a process for producing the same, and the use of the resin composition. Background technique
  • Laser direct structuring (LDS) technology refers to the use of a computer to control the area scanned by a laser.
  • the laser is irradiated onto a part containing a laser-sensitive additive to activate a circuit pattern.
  • the activated area on the part can be electrolessly plated.
  • a metal such as copper, nickel or gold is deposited to produce a conductive pattern on a three-dimensional plastic part.
  • LDS laser direct structuring
  • Moulded Interconnect Device is faster, more streamlined, more cost-effective, and has a wider application area. Its biggest advantage is that it can Reduce the number of components in electronic products and save space.
  • antennas manufactured by LDS technology are widely used in mobile terminals such as smartphones and notebook computers.
  • Sensors manufactured by LDS technology have a minimum wire width of 150 ⁇ and a minimum line width of 150 ⁇ . Not only reduces the number of components, but also saves space and reduces weight.
  • LDS technology is also reflected in its flexibility. If you need to change the conductive path on the component, you only need to change the circuit graphic design in the CAD, no need to redesign the mold. Because LDS technology does not require a mask, the process is simpler and the processing cost is lower. The material science applied to LDS technology has also developed rapidly. Resin The base covers general plastics, engineering plastics and special engineering plastics. A typical application is polycarbonate, polycarbonate and acrylonitrile/butadiene/styrene alloys. LDS antennas made with them have been widely used in smartphones, tablets and notebook computers.
  • Parts used in surface mount technology have special requirements for resin substrates: high temperature resistance.
  • the processing temperature of the SMT process is as high as 270 ° C. At this temperature, the resin matrix cannot be softened or melted, otherwise deformation, foaming, and the like are likely to occur.
  • Materials that can satisfy the SMT process include high temperature nylon, liquid crystal polymer, and polyaryl ether ketone.
  • thermally conductive plastics as a thermally conductive material combines the simplicity of plastic molding with excellent thermal conductivity and allows for the heat transfer of certain metals or ceramics by injection molding.
  • a commonly used thermal conductive material is preferably aluminum, which has a thermal conductivity of up to 150 W/mK. According to the latest research, the heat transfer rate from the metal to the product surface is higher than the rate at which the air convection energy dissipates heat from the surface, and its high heat conduction cannot be effectively realized. At this time, the heat transfer is restricted by convection, relative to the metal. , thermal plastic is the right choice.
  • Thermally conductive plastics have a lower coefficient of thermal expansion (CTE) than aluminum, thus reducing the stress caused by thermal expansion; About 40% lighter than aluminum, it offers greater design freedom than aluminum, and eliminates the need for costly post-processing.
  • CTE coefficient of thermal expansion
  • the use of thermally conductive plastics is more resistant to corrosion, flexibility, and lower cost.
  • the LED industry is a hot industry, and its heat dissipation is becoming more and more important. This is because the light decay of LED or its lifetime is directly related to its junction temperature.
  • the heat dissipation is not good, the junction temperature is high, and the life is short.
  • the Arrhenius equation the temperature will be extended by 2 times for every 10 °C decrease in temperature.
  • the junction temperature not only affects long-term life, but also directly affects short-term luminous efficiency.
  • the heating of the LED will also cause its spectral shift, color temperature increase, forward current increase (at constant voltage supply), reverse current increase, thermal stress increase, and phosphor epoxy aging acceleration. . Therefore, improving the thermal control junction temperature is the most important issue in LED lighting design.
  • the main forms of LED packages are discrete devices and COB (Chip on Board) packages.
  • the die of the discrete device is sealed within the package, and the package functions primarily to protect the die and complete the electrical interconnection.
  • the LED package is to complete the output signal, protect the die from normal operation, output visible light, both electrical parameters, optical design and technical requirements.
  • Discrete devices are required for plug-in or by surface mount process to be attached to the system substrate.
  • the COB package eliminates a bracket and directly packages the chip onto the system board, reducing the thermal resistance of the interface and the bracket itself.
  • the heat dissipation technology has developed to the present day, and the thermal resistance caused by the interface has become more and more prominent.
  • COB reduces the interface, it still needs to be fixed on the heat sink during the application process.
  • the middle interface is hollow and close or add thermal grease. The existence of this interface thermal resistance makes the overall heat dissipation performance not good. Summary of the invention
  • the technical solution adopted by the present invention is a resin composition composed of the following components: a resin matrix of 15-60% by weight ;
  • the resin matrix selected for use in the present invention comprises a thermoplastic, a thermoset, a rubber and an elastomer.
  • the thermoplastic resin includes: polycarbonate (PC), acrylonitrile-butadiene-styrene copolymer (ABS), polycarbonate and acrylonitrile-butadiene-styrene ratio composition (PC/ABS) , liquid crystal polymer (LCP), polyamide (PA), polyphenylene sulfide
  • PPS polyphenylene ether
  • PPE polyphenylene ether
  • PEEK polyetheretherketone
  • PEKK polyetherketoneketone
  • TPI thermoplastic polyimide
  • polyacetal polyethylene ( ⁇ ), polypropylene ( ⁇ ), polystyrene (PS), polytetrafluoroethylene (PTFE), polyacrylates, styrene-acrylonitrile copolymer (SA), poly Butylene terephthalate
  • PBT polyethylene terephthalate
  • PET polycyclohexanediol terephthalate
  • composition comprising at least one of the above polymers.
  • the polyamide resin selected includes an aliphatic polyamide, a semi-aromatic polyamide, or a blend composition of a semi-aromatic polyamide and an aliphatic polyamide.
  • the aliphatic polyamide carbon chain selected is composed of 4 to 36 carbon atoms
  • the typical aliphatic polyamide includes one or more of PA6, PA66, PA610, PA612, PA1010, PA11, PA12, PA1012. Composition, but not limited to these combinations.
  • the semi-aromatic polyamide is composed of a dicarboxylic acid unit and a diamine unit, wherein the dicarboxylic acid unit comprises 45-100 mole percent of aromatic dicarboxylic acid units and 0-55 mole percent of An aliphatic dicarboxylic acid unit of 4 to 12 carbon atoms, and the diamine unit is a linear aliphatic diamine of 4 to 14 carbon atoms, a branched aliphatic diamine or an alicyclic diamine.
  • the aromatic dicarboxylic acid unit comprises terephthalic acid, isophthalic acid, 2-methylterephthalic acid, 2,5-dichloroterephthalic acid, 2,6-dichloro Phthalic acid, 1, 4-naphthalene dicarboxylic acid, 4, 4'-diphenyl phthalate or 2, 2 '-diphenyl phthalic acid.
  • the aliphatic dicarboxylic acid unit comprises 1,4-succinic acid, 1,6-hexanedioic acid, 1,8-octanedioic acid, 1,9-sebacic acid, 1, 10-anthracene. Diacid, l, l l- ⁇ -dioxalic acid, or 1,12-dodecanedioic acid.
  • the linear aliphatic diamine includes 1,4-butanediamine, 1,6-hexanediamine, 1,8-octanediamine, 1,9-nonanediamine, 1, 10- Decane diamine, l, l l- ⁇ monocarbodiamine, or 1, 12-dodecadiamine.
  • the branched aliphatic diamine comprises 2-methyl-1, 5-pentanediamine, 3-methyl-1, 5-pentanediamine, 2,4-dimethyl-1, 6-hexanediamine, 2, 2, 4-trimethyl-1,6-hexanediamine, 2,4,4-trimethyl-1,6-hexanediamine, or 2-methyl-1, 8-octanediamine or 5-methyl-1,9-nonanediamine.
  • the alicyclic diamine comprises cyclohexyldiamine, methylcyclohexyldiamine or 4,4'-diaminodicyclohexylformamidine.
  • thermosetting plastic comprises: an epoxy resin, a phenolic resin, an unsaturated polyester, a polyimide, or a composition comprising at least one of the foregoing polymers.
  • the rubber comprises natural rubber and synthetic rubber, or a composition comprising at least one of the foregoing polymers.
  • the elastomer comprises a styrene elastomer, a polyolefin elastomer, a polyester bomb
  • the thermally conductive filler selected for the present invention comprises: aluminum oxide, aluminum nitride, silicon nitride, magnesium oxide, silicon carbide, boron nitride, carbon fiber, carbon nanotube, carbon black, graphite, aluminum hydroxide, zinc oxide. , magnesium oxide, magnesium hydroxide, metal filler or a combination thereof.
  • the thermally conductive filler is boron nitride
  • the boron nitride may be cubic boron nitride, hexagonal boron nitride, amorphous boron nitride, or diamond boron nitride, which may be in the form of spheres, sheets or fibers. use.
  • the spherical structure heat conductive filler has an average particle diameter of 10 ⁇ ⁇ to 200 ⁇ , preferably 15 ⁇ 150 150 ⁇ m, more preferably 20 ⁇ ! ⁇ ⁇ ⁇
  • the thermally conductive filler of the sheet structure has a diameter to thickness ratio of 10 to 100, preferably 10 to 80, more preferably 10 to 50, and a fiber diameter of 3 to 25 ⁇ m.
  • the resin composition of the present invention is an insulating heat conductive material, and the surface resistivity of the resin composition is not less than 10 13 ⁇ . Lwt%-10 ⁇ % ⁇ The amount of the carbon nanotubes, carbon black, graphite is preferably 0. lwt% - 10wt%.
  • the laser sensitive additive plays an important role in the laser processing of the resin composition.
  • the laser beam is swept over the surface of the product made of the resin composition, and the resin matrix is ablated to form an uneven region, which can increase the bonding strength between the electroless metal plating layer and the resin matrix; on the other hand, the laser sensitive additive is in the laser Under the action of the metal particles, the metal particles are adhered to the uneven resin matrix.
  • the metal particles act as an activation center, and the metal ions in the electroless plating solution are selectively deposited. A metal film is formed.
  • the laser sensitive additive selected for use in the present invention is a high temperature resistant inorganic additive capable of withstanding temperatures in excess of 600 °C.
  • the smallest structural unit included in the laser-sensitive additive is a tetrahedral structure and an octahedral structure.
  • the oxygen atoms occupy all the centroid positions, forming a close packing, and two different metal ions are respectively distributed to the center of the tetrahedron.
  • the octagonal center position The center of the tetrahedron is a gap between the tetrahedrons surrounded by four oxygen ions, and the center of the octahedron is a gap between the octahedrons surrounded by six oxygen ions.
  • a complete unit cell structure contains eight tetrahedral atoms, sixteen octahedral atoms, and thirty-two oxygen atoms, so in its structural unit, the ratio of the corresponding simplest atoms is one. : twenty four.
  • X is a metal element, a metal atom derived from the lanthanum, group IB, group II B, group VIB, group VIIB, and ring of the periodic table, including metal chromium, manganese, iron, cobalt, nickel, copper, zinc, palladium, aluminum Any one of them;
  • Y is a metal element derived from a metal atom of the lanthanum, IB, lanthanum, VIB, VIIB, and ring of the periodic table, including metal chromium, manganese, iron, cobalt, nickel , copper, zinc, palladium, aluminum; any specific reference can refer to the textbook "Basic Crystal Science", author Qin Shan, Peking University Press.
  • the tetrahedral central atom therein is preferably derived from a transition metal atom, most preferably from the fourth period.
  • the octahedral central atom therein is preferably derived from a transition metal atom, most preferably from the fourth period.
  • the amount of the laser-sensitive additive selected for use in the present invention is 5 to 12% by weight, preferably 5 to 9 % by weight.
  • the addition amount of the laser sensitive additive is more than 15% by weight, the parts are liable to cause deterioration phenomenon such as overflow plating during the electroless plating process, and affect the electronic and electrical functions of the workpiece.
  • additives selected for use in the present invention include halogen-free flame retardants, flame retardant synergists, curing agents, mold release agents, antioxidants, and lubricants.
  • the resin composition is required to meet the UL 94 V-0 flame retardant rating, but at the same time, red phosphorus, halogenated flame retardant flame retardants should not be used.
  • materials include polyphenylene sulfide (PPS), liquid crystal polymer (LCP), and polyaryletherketone (PAEK).
  • the usual means of flame retardant modification is the addition of a flame retardant.
  • different resin matrices have a strong selectivity for flame retardants.
  • the flame retardancy of the polycarbonate can be improved by increasing the carbon forming ability of the polycarbonate.
  • the optional flame retardant includes a sulfonate flame retardant, phosphonic acid.
  • an organosilicon oxime flame retardant can also be used.
  • the halogen-free flame retardant selected has the following formula:
  • R1 and R2 are the same or different and include a linear or branched fluorenyl group and/or an aryl group of 1 to 6 carbon atoms.
  • R3 includes a linear or branched fluorenylene group of 1 to 10 carbon atoms, an arylene group of 6 to 10 carbon atoms, a fluorenylene arylene group or an aryl fluorenylene group.
  • M includes metal ions in the second and third main or subgroups of the periodic table.
  • the M metal ion is preferably a calcium ion or an aluminum ion.
  • m 2 or 3.
  • n 1 or 3.
  • X is 1 or 2.
  • the halogen-free flame retardant used includes dimethylphosphinate, ethylmethylphosphinate, diethylphosphinate, methyl-n-propylphosphinate, Two (a Mercaptophosphonic acid) formamidine salt, 1,2-bis(methylphosphinic acid) acetamidine salt, 1,6-bis(methylphosphinic acid) hexamethylene salt, 1,4-di(methyl) Phosphonic acid) phenyl salt, methylphenylphosphinate, diphenylphosphinate.
  • additives also include inorganic fillers such as glass fibers, boron fibers, titanium dioxide, talc, mica, barium titanate, glass beads, calcium copper titanate, kaolin, and the like.
  • the resin composition of the present invention and the article produced using the resin composition are electrically insulating, and have a surface resistivity of not less than 10 13 ⁇ .
  • the present invention is required to provide a method for producing a resin composition.
  • the preparation method of the resin composition according to the present invention is as follows:
  • Weighing the material Weigh the material according to the following weight percentage: 15_60 wt% thermoplastic or elastomer resin matrix; 30_70 wt% thermally conductive filler; 5-12 wt% laser sensitive additive; 0-153 ⁇ 4 ⁇ /. Other additives;
  • Mixing material adding a resin matrix, a part of thermally conductive filler, a laser sensitive additive, and other additives to a high-speed mixer, and mixing uniformly;
  • Extrusion The uniformly mixed material is fed from the main feed hopper, and the remaining part of the thermally conductive filler is fed from the side feed hopper, extruded by a common twin-screw extruder, cooled, and pelletized to obtain the target of the resin composition. Parts.
  • the resin composition of the present invention can also be obtained by the following preparation method: Weighing the material: Weigh the material according to the following weight percentage: 15_60 wt% of thermosetting plastic or rubber resin matrix; 30_70 wt% of thermally conductive filler; 5-123 ⁇ 4 ⁇ % laser sensitive additive; 0_153 ⁇ 4 ⁇ % of other additives;
  • Mixture Mix the resin matrix, thermal conductive filler, laser sensitive additive, and other additives evenly;
  • Hot press forming The obtained resin composition is charged into a suitable mold, heat-treated, and the resin composition is molded by a press molding method as a target article.
  • the resin composition of the invention has excellent high temperature resistance and good thermal conductivity, and can selectively deposit metals such as copper, nickel and gold in a laser scanned region, and can be used for surface mount technology (SMT).
  • SMT surface mount technology
  • the main application is in the field of electrical and electronic components.
  • LDS laser direct structuring
  • the resin composition is molded by a molding process such as injection molding, extrusion or molding, and a circuit is formed on the workpiece by laser direct structuring, and then the electron is directly formed.
  • LED chip can be realized without interface thermal resistance package, and the system circuit board and heat sink can be integrated into one body to achieve efficient heat dissipation and prolong the life of LED lighting.
  • Figure 1 is a schematic diagram of the structure of a laser sensitive additive. detailed description
  • the present invention discloses a resin composition having a Laser Direct Structuring function, a method of preparing the resin composition, and an application of the resin composition.
  • the resin composition consists of the following components:
  • Resin matrix 15-60% by weight ;
  • It is a heavy metal oxide which may contain one or more metal oxides of copper, manganese, iron, zinc, nickel, aluminum, titanium, cobalt, magnesium, lanthanum, tin. On the one hand, they are good conductors of heat relative to the resin matrix, enabling rapid electronic components, electronic components, and
  • the laser-sensitive additive used in the present invention has a small particle diameter of 1.5 ⁇ m -2. 1 ⁇ m and a specific surface area of more than 35,000 cm 2 /cm 3 . It is evenly distributed in the gap of the large particle heat conductive filler, which can effectively increase the contact area of the heat conduction network skeleton and form a plurality of heat conduction networks, thereby improving the heat conduction efficiency of the composition.
  • the preparation method of the resin composition of the present invention is as follows:
  • thermoplastic or thermosetting plastic, or rubber, or elastomer resin matrix
  • 30_70wt% thermally conductive filler 5_12wt% laser sensitive additive
  • 0_153 ⁇ 4 ⁇ % other additives 0_153 ⁇ 4 ⁇ % other additives
  • the obtained mixed material is extruded, cooled, and pelletized by a twin-screw extruder to obtain a target product; or the obtained mixed material is charged into a mold, and heat-press molded to obtain a target article.
  • the resin composition of the present invention is mainly used for the production of electrical and electronic components, including circuit substrates such as electronic components, bracket materials for electronic components, bases for high-power LED lamps, or circuit boards.
  • the electronic components can be connected to the circuit substrate after the LDS process is formed by SMT. Either way, there is an interface thermal resistance between the electronic component and the substrate. Due to the low thermal conductivity of conventional substrates (such as PCB boards), the heat generated by electronic components cannot be diffused into the environment, which can seriously affect the service life of assembled products, especially for heat-sensitive electronic components. Working in a high temperature environment, performance damage is more obvious Obvious. If there is an interface thermal resistance, the heat dissipation effect of the electronic components will be worse, and the service life will be seriously shortened.
  • the resin composition provided by the present invention has a high thermal conductivity, and the electronic component is directly mounted on a circuit formed by the LDS process, and the heat dissipation effect can be remarkably improved. This is because the electronic components are directly packaged on a substrate with high thermal conductivity to facilitate heat dissipation.
  • the conductive traces are deposited on the substrate by an electroless plating process, and the conductive traces and the substrate constitute a perfect whole. There is no interface resistance and the thermal conductivity will be better.
  • the laser sensitive additives selected in the following examples are copper-chromium-type laser-sensitive additives and copper-manganese-type laser-sensitive additives, and their structures are shown in FIG.
  • the copper-manganese additive listed in the present invention is one of the best choices, and no toxic metal ions are generated in the laser process and the non-electroless plating process. Under the action of the laser, the crystal lattice of the laser sensitive additive is destroyed, and the inside Metal elements are released, accompanied by redox reactions.
  • chromium in copper-chromium-based laser-sensitive additives changes from a low-cost state to a high-valence state, producing Cr 6+ , which is a toxic ion.
  • the manganese in the copper-manganese laser-sensitive additive is also changed from a low-valent state to a high-valent state, but it is non-toxic, which is environmentally friendly.
  • the resin matrix is made of poly(p-phenylene dihydrazide diamine (PA10T, from Blonde Technology Co., Ltd.) 35wt%
  • thermal conductive filler is selected from boron nitride 303 ⁇ 4 ⁇ % and magnesium oxide 20wt%
  • copper-manganese laser sensitive additive from giant hair Technology Co., Ltd.
  • other additives use nano-alumina 2wt%
  • glass fiber from Jushi Group Co., Ltd.) 8wt%.
  • the resin matrix is made of polyparaphenylene dihydrazide diamine, 28wt%, and the thermal conductive filler is nitrided. Boron 303 ⁇ 4 ⁇ /. 20wt% of magnesium oxide, 12wt% of copper-manganese type laser sensitive additive, 2wt% of other additives, 8wt% of glass fiber.
  • Polyethylene resin matrix selected terephthalamide decanediamine 40wt%, the thermally conductive filler selected boron 30wt Q / P magnesium 20wt%, or copper-manganese-type laser-sensitive additive Owt%, of other additives selected nano-alumina 2wt%, glass fiber 8wt%.
  • the resin matrix is made of polytrimethylene dihydrazide diamine 37wt%
  • the thermal conductive filler is boron nitride 30wt Q / P magnesium oxide 20wt%
  • copper manganese type laser sensitive additive 3wt% other additives use nanometer alumina 2wt%, glass fiber 8wt%.
  • the selected boron nitride was a microscopic sheet-like structure having an average particle diameter of about 150 ⁇ m and a diameter to thickness ratio of about 20; magnesium nitride was a microscopic spherical structure.
  • the average particle diameter of about 20 ⁇ ⁇ ; nano-alumina microscopic spherical structure, an average particle diameter of about 20 ⁇ ⁇ ; average particle diameter of the copper-manganese-type laser-sensitive additive is 1.8 persons 0. 3 ⁇ m, a specific surface area More than 35000cm7cm 3 .
  • Boron nitride is a heat-conductive material with a large-diameter sheet-like structure.
  • It mainly functions as a heat-conducting network skeleton in a resin matrix, and a small-diameter spherical structure of magnesium oxide is coated with alumina, uniformly distributed in a resin matrix, and tends to Distributed between the sheet-like structures of boron nitride to form a thermally conductive network.
  • the magnesium oxide in each of the above embodiments is added to a high-speed mixer, and then the nano-alumina is added to continue to uniformly mix, so that the nano-alumina is uniformly adhered to the outer surface of the magnesium oxide, and then the copper-manganese-type laser-sensitive additive and the poly-pair
  • the phthalic acid diamine resin was uniformly mixed, it was fed from the main feed hopper of the twin-screw extruder.
  • the glass fiber is fed from the first side feed port, the boron nitride is fed from the second side feed port, and is extruded and granulated to obtain a heat conductive LDS resin material.
  • LDS resin material with thermal conductivity needs to test thermal conductivity, film thickness test, 100 Cross-Cut Test.
  • the thermal conductivity test standard is ISO 8301.
  • the film thickness test is to test the thickness of the metal film deposited on the LDS material in the absence of electrochemical plating. The industry requires that the film thickness distribution within 7-12 ⁇ ⁇ is acceptable.
  • 100-gram test that is, using a utility knife to cut 100 lmm*lmm squares on the metal film, stick it with 3M 610 tape and place it for about 2 minutes, then pull it up vertically, and the falling area of the metal film is less than 5%.
  • the surface resistivity test standard is ASTM D257 o
  • the test results are shown in Table 1.
  • the amount of the laser-sensitive additive is less than 5% by weight, the amount of metal particles released by the laser is too small, and copper, nickel, and gold cannot be obtained in the absence of electrochemical plating.
  • the addition amount is 5-12%, sufficient metal particles are released under the action of laser, and act as an activation center in the process of electroless plating, and copper, nickel and gold can be smoothly plated.
  • Polyphenylene sulfide (purchased from Sichuan Deyang Chemical Co., Ltd.) 17 wt%, boron nitride 40 wt%, magnesium oxide 30 wt%, copper chromium type laser sensitive additive 5 wt%, nano alumina 3 wt%, carbon fiber 5 wt%.
  • Sichuan Deyang Chemical Co., Ltd. 17 wt%, boron nitride 40 wt%, magnesium oxide 30 wt%, copper chromium type laser sensitive additive 5 wt%, nano alumina 3 wt%, carbon fiber 5 wt%.
  • the test results show that the thermal conductivity of the material is 3.36 W/mK, the thickness of the metal film is 7.68 um, and the peeling area of the metal film of the test is ⁇ 5%.
  • Thermotropic liquid crystal polymer (from Blonde Technology Co., Ltd.) 58 wt%, aluminum nitride 10 wt%, zinc oxide 10 wt%, copper chromium type laser sensitive additive 12 wt%, carbon fiber 10 wt%.
  • the liquid crystal polymer has a melting point of 325 ° C, a processing temperature of not higher than 350 ° C, and nitriding Aluminum is a microscopic sheet-like structure having an average particle diameter of about ⁇ ⁇ ⁇ and a diameter to thickness ratio of about 25; the zinc oxide is a microscopic spherical structure having an average particle diameter of 15 ⁇ m.
  • the copper-chromium-based laser-sensitive additive has an average particle diameter of 1. 8 ⁇ 0.3 ⁇ m and a specific surface area of more than 35,000 cm 2 /cm 3 .
  • the test results show that the thermal conductivity of the material is 1. 10 W/mK, the thickness of the metal film is 10.55 um, and the peeling area of the metal film of the test is ⁇ 5%.
  • the resin matrix was selected from polyamide PA6 18 wt% and polypropylene resin PP 3 wt%, and the thermal conductive filler was boron nitride 50 wt% and graphite 20 wt%, and copper manganese type laser sensitive additive 9 wt%. After the addition of boron nitride, the fluidity of the melt deteriorates. Graphite acts as a lubricant in the resin matrix, reducing the viscosity of the melt, facilitating processing, and also improving the thermal conductivity of the composition.
  • the selected PA6 has a density of about 1.13 g/cm 3 , a melting point of 215 ° C, and a processing temperature of not higher than 250 ° C.
  • the selected PP is an isotactic polypropylene having a density of about 1.04 g/cm 3 , processed.
  • the temperature is not higher than 250 ° C; the average particle diameter of the copper-manganese laser-sensitive additive is 1. 8 ⁇ 0.3 ⁇ m, and the specific surface area is greater than 35000 cm 2 /cm 3 .
  • the resin matrix and the copper-manganese laser-sensitive additive are uniformly mixed in a high-speed mixer, and then added from the main feed port of the twin-screw extruder, boron nitride is added from the first side feed hopper, and graphite is fed from the second side feed hopper. It is added, extruded, cooled, and pelletized to obtain a resin composition.
  • test standard is referred to in Example 1.
  • the test results show that the thermal conductivity is 3.47W/mK, the thickness of the metal film is 9.58um, and the peeling area of the metal film of the test is ⁇ 5%.
  • Bisphenol A epoxy resin (Epoxy 828) 25wt%, boron nitride 45wt%, carbon fiber 20wt%, copper manganese type laser sensitive additive 5wt%, acid anhydride curing agent (MT-500TZ) 4. 95wt%, 2-ethyl- 4-methylimidazole (2E4MZ) 0. 05wt% o
  • the above components are uniformly mixed and poured into the mold.
  • the resin composition was prepared by curing in a hot air oven at 100 ° C for 2 hours and then at 130 ° C for 3 hours.
  • test standard is referred to in Example 1.
  • the test results show that the thermal conductivity is 2.10W/mK, the thickness of the metal film is 7. Hum, and the peeling area of the metal film of the test is ⁇ 5%.
  • the singularity of the average particle diameter of the copper-manganese-type laser-sensitive additive is 1. 8 ⁇ 0. 3 ⁇ ⁇ , specific surface area greater than 35000 cm 2 /cm 3 .
  • the test results show that the thermal conductivity of the material is 0. 78 W / mK, the thickness of the metal film is 5. 73 um, the area of the metal film is 5%, the combustion performance meets the UL 94 V_0 standard, and the thickness of the spline is 1. 0mm.
  • Example 9 The test results of Examples 5-8 and Comparative Example 9 are shown in Table 2.
  • Table 2 Test Results Laser Sensitive Additives Thermal Conductive Filler Thermal Conductivity Film Thickness Test 100 Grid Test wt% wt% W/mK um Example 5 6 70 3. 36 7. 68 0K Example 6 12 30 1. 10 10. 55 0K Implementation Example 7 9 70 3. 47 9. 58 0K Example 8 5 65 2. 10 7. 11 0K Comparative Example 9 4 25 0. 78 5. 73 NG
  • the specific gravity ranges from 5 to 12 wt%, and the preferred specific gravity of the thermally conductive filler ranges from 30 to 70 wt%.
  • the resin matrix is selected from the composition of high temperature resistant polyamide PA10T and aliphatic polyamide PA66, wherein PA10T is 10wt%, PA66 is 20wt%, thermal conductive filler is boron nitride 30wt% and magnesia 20wt%, copper manganese laser sensitive additive 10wt%
  • the other additives used halogen-free flame retardant was dimethyl phosphinate (purchased from Clariant) 8 wt%, boehmite 2 wt%.
  • the processing temperature of the twin screw is between 290 °C and 330 °C.
  • the resin matrix and the boehmite copper-manganese type laser sensitive additive are uniformly mixed in a high-speed mixer and then added from the main feeding port of the twin-screw extruder, and boron nitride is added from the first side feeding hopper, and the halogen-free flame retardant is added. It was added from the second side feed hopper, extruded, cooled, and pelletized to obtain a resin composition.
  • test standard is referred to in Embodiment 1.
  • the test results show that the thermal conductivity is 1.96W/mK, the thickness of the metal film is 8.39um, and the peeling area of the metal film is 100%.
  • the thickness of the metal film is 1. Omm-3. 0mm.
  • the film thickness test and the 100-gram test can be passed through the film thickness of 15-60 wt%; the heat conductive filler 30-70 wt% ; the laser sensitive additive 5_12 wt%; and other additives 0-15 wt%, and the thermal conductivity is good. .
  • the resin composition of the present invention has excellent high temperature resistance and good thermal conductivity, and can selectively deposit copper, nickel, gold and the like in a laser-scanned region, and can be used for surface mount technology (SMT).
  • SMT surface mount technology
  • the parts are mainly used in the field of electrical and electronic components, such as LED light radiators.

Abstract

本发明提供一种具有激光直接成型(Laser Direct Structuring)功能的树脂组合物、制备所述树脂组合物的方法以及该树脂组合物的应用。所述树脂组合物由以下组分组成:树脂基体 15-60wt%;导热填料 30-70wt%;激光敏感添加剂 5-12wt%;以及其他添加剂 0-15wt%,其中激光敏感添加剂的化学通式为XY2O4,等轴晶系,轴长a=b=c,轴角α=β=γ=90°;其中X与Υ均为金属元素,来自元素周期表中第IIIA族、IB族、IIΒ族、VIB族、VIIB族、VIII族。本发明所述的树脂组合物耐高温且导热性好,能够在激光扫描过的区域内有选择性地沉积铜、镍、金等金属,可用于表面贴装技术(SMT)的制件。

Description

具有激光直接成型功能的树脂组合物、其制备方法以及该树脂组合物 的应用 技术领域
本发明涉及一种树脂组合物,尤其涉及具有激光直接成型(Laser Direct Structuring) 功能的导热树脂组合物, 其制备方法以及该树脂 组合物的应用。 背景技术
激光直接成型(LDS )技术是指利用计算机控制激光扫描的区域, 将激光照射到含有激光敏感添加剂的制件上, 活化出电路图案, 该制 件上被活化的区域可以在无电化学镀中沉积金属铜、 镍、 金等金属, 从而实现在三维塑料制件上制造出导电图案。
随着激光直接成型 (LDS ) 技术的快速发展, 模塑互联器件 (Moulded Interconnect Device ) 的生产速度更迅捷, 流程更简化, 成本更可控, 应用领域更宽广, 其最大的优势在于, 它能够减少电子 产品的元器件数量并节约空间。 比如, 采用 LDS技术制造的天线被广 泛地应用在智能手机、笔记本电脑等移动终端上, 采用 LDS技术制造 的传感器, 最小导线宽度可达 150 μ πι, 最小线间宽度可达 150 μ πι, 这不但减少了元器件的数量, 还达到了节约空间和减重的目的。
此外, LDS技术的优势还体现在它的灵活性上。 如果需要改变元 器件上导电路径, 只需要更改 CAD中的电路图形设计即可, 不需重新 设计模具。 因为 LDS技术不需要掩膜, 所以其加工过程更加简便, 加 工成本更低。应用于 LDS技术的材料科学也得到了快速的发展。树脂 基体覆盖了通用塑料、工程塑料以及特种工程塑料。其中比较典型的 应用是聚碳酸酯、聚碳酸酯与丙烯腈 /丁二烯 /苯乙烯的合金, 用它们 来制作的 LDS天线已经广泛地应用在智能手机、平板电脑以及笔记本 电脑上。
应用于表面贴装技术 (SMT ) 的制件, 对树脂基体有着特殊的要 求: 耐高温。 通常, SMT制程的加工温度高达 270°C, 在此温度下, 树脂基体不能软化或熔化, 否则容易出现变形、 起泡等不良现象。 能 够满足 SMT制程的材料有高温尼龙、液晶聚合物以及聚芳醚酮等聚合
电子技术及材料科技飞速发展,电子电气元器件向小型化密集化 发展, 集成电路中产生大量的热, 而热量是影响设备可靠性的重要因 素。据统计, 电子元器件温度每升高 2 °C,可靠性下降 10%;温升 50°C 的寿命只有温升 25 °C时寿命的 1/6。这就要求材料既具有优良的电绝 缘性和低的线性热膨胀系数, 又具有优良导热性能。 可以说, 没有新 的导热塑料制备的散热和热传导材料,将功能更强大的微电子器件放 入更小的空间是不可能的。
用导热塑料作为导热材料,能够将塑料成型的简易性与优异的热 传导性相结合,可以通过注射成型实现某些金属或陶瓷一样的热传递 能力。 常用的导热材料优选铝, 其导热系数可达到 150W/mK。 根据最 新的研究发现,金属至产品表面的传热速率如果高于空气对流能将热 从表面散走的速率, 其高热传导就不能有效的实现, 此时热迁移受对 流限制, 相对金属而言, 导热塑料就是适宜之选。 导热塑料具有比铝 还低的热膨胀系数 (CTE) , 因此降低了热膨胀引起的应力; 导热塑料 比铝轻约 40%, 提供了比铝更大的设计自由度, 还省去了高成本的后 加工过程, 使用导热塑料更耐腐蚀、 更柔韧、 成本更低。
现在, LED产业是热门产业, 其散热越来越为人们所重视, 这是 因为 LED的光衰或其寿命直接与其结温有关。散热不好结温就高, 寿 命就短, 依照阿雷尼乌斯方程温度每降低 10°C寿命会延长 2倍。 而 且, 结温不但影响长时间寿命, 也还直接影响短时间的发光效率。 此 外, LED的发热还会使得其光谱移动、 色温升高、 正向电流增大 (恒 压供电时)、 反向电流也增大、 热应力增高、 荧光粉环氧树脂老化加 速等种种问题。所以, 改善散热控制结温是 LED照明设计中最为重要 的一个问题。
目前 LED封装的主要形式有分立器件、 COB ( Chip on board) 封 装两大类。 一般情况下, 分立器件的管芯被密封在封装体内, 封装的 作用主要是保护管芯和完成电气互连。而 LED封装则是完成输出电信 号, 保护管芯正常工作, 输出可见光, 既有电参数, 又有光参数的设 计及技术要求。分立器件在应用时, 需要插件或者通过表面贴装工艺 悍接到系统基板上。 COB封装则省去一个支架, 直接将芯片封装到系 统电路板上, 减少了界面和支架本身的热阻。 然而, 散热技术发展到 今天, 界面引起的热阻越来越突出。 COB虽然减少了界面, 但是在应 用过程中依然需要固定在散热器上,中间界面为中空紧贴或者加上导 热硅脂。 这一界面热阻的存在使得整体散热效能并不佳。 发明内容
鉴于以上所述, 本发明有必要提供一种具有 LDS特征、且导热性 本发明所采用的技术方案是,一种树脂组合物,由以下成分组成: 树脂基体 15-60wt%;
导热填料 30-70wt%;
激光敏感添加剂 5_12wt%; 以及
其他添加剂 0-15wt%;
其中, 所述激光敏感添加剂的化学通式为 XY204, 等轴晶系, 参 见附图 1, 轴长 a=b=c, 轴角 α = β = Υ =90° ; X与 Υ均为金属元素, 来自元素周期表中第 ΠΙΑ族、 I B族、 II B族、 VIB族、 VIIB族、 或環 族。
优选地,本发明所选用的树脂基体包括热塑性塑料、热固性塑料、 橡胶和弹性体。 其中, 热塑性树脂包括: 聚碳酸酯 (PC )、 丙烯腈- 丁二烯-苯乙烯共聚物 (ABS)、 聚碳酸酯与丙烯腈 -丁二烯-苯乙烯任 意比组合物(PC/ABS)、 液晶聚合物(LCP)、 聚酰胺(PA)、 聚苯硫醚
(PPS)、 聚苯醚 (PPE)、 聚砜、 聚芳酯、 聚醚醚酮 (PEEK)、 聚醚酮 酮(PEKK)、 聚醚醚酮酮(PEEKK)、 热塑性聚酰亚胺(TPI )、 聚縮醛、 聚乙烯 (ΡΕ)、 聚丙烯 (ΡΡ)、 聚苯乙烯 (PS )、 聚四氟乙烯 (PTFE)、 聚丙烯酸酯类、 苯乙烯-丙烯腈共聚物(SA)、 聚对苯二甲酸丁二醇酯
(PBT) 以及聚对苯二甲酸乙二醇酯 (PET)、 聚对苯二甲酸环己二醇 酯, 或者包括至少一种上述聚合物的组合物。
更优选地, 所选用的聚酰胺树脂包括脂肪族聚酰胺、半芳香族聚 酰胺、 或者半芳香族聚酰胺与脂肪族聚酰胺的共混组合物。
更优选地, 所选用脂肪族聚酰胺碳链由 4-36个碳原子组成, 典 型的脂肪族聚酰胺包括 PA6、 PA66、 PA610、 PA612 , PA1010、 PA11、 PA12、 PA1012中的一种或者多种的组合物, 但不局限于这些组合。 更优选地, 所述半芳香族聚酰胺由二元羧酸单元和二胺单元组 成, 其中二元羧酸单元包括 45-100摩尔百分比的芳香族二羧酸单元 和 0-55摩尔百分比的具有 4-12个碳原子的脂肪族二羧酸单元,二胺 单元为 4-14个碳原子直链脂肪族二元胺、 支链脂肪族二元胺或脂环 族二元胺。
更进一歩优选地, 芳香族二羧酸单元包括对苯二甲酸、 间苯二甲 酸、 2-甲基对苯二甲酸、 2, 5-二氯对苯二甲酸、 2, 6-二氯对苯二甲酸、 1, 4-萘二甲酸、 4, 4' -联苯二甲酸或 2, 2 ' -联苯二甲酸。
更进一歩优选地, 脂肪族二羧酸单元包括 1,4-丁二酸、 1,6-己 二酸、 1,8-辛二酸、 1,9-壬二酸、 1, 10-癸二酸、 l,l l- ^一垸二酸、 或 1, 12-十二垸二酸。
更进一歩优选地, 直链脂肪族二元胺包括 1,4-丁二胺、 1,6-己 二胺、 1,8-辛二胺、 1,9-壬二胺、 1, 10-癸二胺、 l,l l- ^一碳二胺、 或 1, 12-十二碳二胺。
更进一歩优选地, 支链脂肪族二元胺包括 2-甲基 -1, 5-戊二胺、 3-甲基 -1, 5-戊二胺、 2, 4-二甲基 -1, 6-己二胺、 2, 2, 4-三甲基 -1, 6- 己二胺、 2, 4, 4-三甲基 -1, 6-己二胺、 或 2-甲基 -1, 8-辛二胺或 5-甲 基 -1, 9-壬二胺。
更进一歩优选地, 脂环族二元胺包括环己垸二胺、 甲基环己垸二 胺或 4, 4' -二氨基二环己基甲垸。
优选地, 热固性塑料包括: 环氧树脂、 酚醛树脂、 不饱和聚酯、 聚酰亚胺, 或者包括至少一种前述聚合物的组合物。
优选地, 橡胶包括天然橡胶和合成橡胶, 或者包括至少一种前述 聚合物的组合物。
优选地, 弹性体包括苯乙烯类弹性体、 聚烯烃类弹性体、 聚酯弹 优选地, 本发明所选用的导热填料包括: 氧化铝、 氮化铝、 氮化 硅、 氧化镁、 碳化硅、 氮化硼、 碳纤维、 碳纳米管、 炭黑、 石墨、 氢 氧化铝、 氧化锌、 氧化镁、 氢氧化镁、 金属填料或者它们的组合物。
更优选地, 所述导热填料为氮化硼, 氮化硼可以是立方氮化硼、 六方氮化硼、 无定形氮化硼、 菱形氮化硼, 它可以以球状、 片状或是 纤维形式使用。
其中, 球状结构导热填料的平均粒径在 10 μ πι〜200 μ πι, 优选 15 μ πι〜150 μ πι, 更优选 20 μ π!〜 ΙΟΟ μ πι, 片状结构导热填料的径厚 比在 10〜100,优选 10-80,更优选 10-50,纤维直径分布在 3_25 μ m。
本发明所述的树脂组合物为绝缘导热材料,树脂组合物的表面电 阻率不小于 1013 Ω。 导热填料中使用的碳纳米管、 炭黑、 石墨的添加 量优选为 0. lwt%-10wt%。
所述激光敏感添加剂对树脂组合物在激光加工过程中起着重要 的作用。激光光束在树脂组合物制成的制品表面扫过, 将树脂基体烧 蚀掉, 形成凹凸不平的区域, 可以增加化学镀金属层与树脂基体的粘 结强度; 另一方面, 激光敏感添加剂在激光的作用下, 还原出金属颗 粒附着在凹凸不平的树脂基体上, 在后续无电化学镀中, 这些金属颗 粒起到活化中心的作用,促使化学镀液中的金属离子有选择性地沉积 下来, 形成金属薄膜。
本发明所选用的激光敏感添加剂是一种耐高温无机添加剂,所能 够承受的温度超过 600°C。 请参阅图 1, 激光敏感添加剂中所包含的 最小结构单元为四面体结构和八面体结构。其中氧原子占据所有面心 位置, 组成密堆积, 两种不同的金属离子分别分布到四面体中心位置 和八面体中心位置。四面体中心位置为四个氧离子围成的四面体中间 的空隙, 八面体中心位置为六个氧离子围成的八面体中间的空隙。通 常, 一种完整的晶胞结构中含有八个四面体原子、十六个八面体原子 以及三十二个氧原子, 所以在其结构单元中, 其对应的最简原子个数 的比例为 1 : 2 : 4。
优选地, 本发明所选用的激光敏感添加剂其化学通式为 XY204, 属等轴晶系,轴长 a=b=c,轴角 α = β = γ =90° ; 其中, X为金属元素, 来自元素周期表中第 ΠΙΑ族、 I B族、 II B族、 VIB族、 VIIB族、 環族 的金属原子, 包括金属铬、 锰、 铁、 钴、 镍、 铜、 锌、 钯、 铝中的任 意一种; Y为金属元素,来自元素周期表中第 ΙΠΑ族、 I B族、 Π Β族、 VIB族、 VIIB族、 環族的金属原子, 包括金属铬、 锰、 铁、 钴、 镍、 铜、 锌、 钯、 铝的任意一种; 具体说明可参考教材 《晶体学基础》, 作者秦善, 北京大学出版社出版。
其中的四面体中心原子优选来自于过渡金属原子,最优选来自于 第四周期。
其中的八面体中心原子优选来自于过渡金属原子,最优选来自于 第四周期。
本发明所选用的激光敏感添加剂的量为 5-12wt%, 优选的添加量 为 5-9wt%。当激光敏感添加剂的添加量大于 15wt%时, 制件在无电化 学镀的过程中容易引起溢镀等劣化现象, 影响制件的电子电气功能。
优选地, 本发明所选用的其他添加剂包括无卤阻燃剂, 阻燃协效 剂, 固化剂, 脱模剂, 抗氧剂, 润滑剂。
通常, 在产品应用中, 树脂组合物要求能够满足 UL 94 V-0阻燃 等级, 但同时不得使用红磷、 有卤阻燃剂类的阻燃剂。对于那些具有 自阻燃特性的材料, 不需要进行阻燃特性的改性即可满足要求, 这些 材料包括聚苯硫醚(PPS ) , 液晶聚合物(LCP ) , 以及聚芳醚酮(PAEK) 等。
然而, 多数高分子材料本身是具有可燃性的, 对其进行阻燃改性 的通常手段便是添加阻燃剂。 由于不同的阻燃剂的阻燃机理不同, 不 同的树脂基体对阻燃剂有很强的选择性。 如, 针对树脂基体为 PC或 PC/ABS 的树脂组合物, 可通过增加聚碳酸酯的成碳能力来提高其阻 燃性能, 可选用的阻燃剂包括磺酸盐类阻燃剂, 膦酸酯类阻燃剂, 还 可以使用有机硅氧垸类阻燃剂。
而针对树脂基体为聚酰胺组合物的树脂组合物,所选用的无卤阻 燃剂的通式为:
Figure imgf000010_0001
其中, Rl、 R2相同或不同, 包括线型或支化的 1-6个碳原子的 垸基和 /或芳基。
R3包括线型或支化的 1-10个碳原子的亚垸基、 6-10个碳原子的 亚芳基、 垸基亚芳基或芳基亚垸基。
M包括元素周期表中第二和第三主族或副族中的金属离子。 M金 属离子优选钙离子或铝离子。
m为 2或 3。
n为 1或 3。
X为 1或 2。
所述其他添加剂中, 所使用的无卤阻燃剂包括二甲基次膦酸盐、 乙基甲基次膦酸盐、 二乙基次膦酸盐、 甲基正丙基次膦酸盐、 二(甲 基次膦酸) 甲垸盐、 1,2-二(甲基次膦酸) 乙垸盐、 1,6-二(甲基次 膦酸) 己垸盐、 1,4-二(甲基次膦酸)苯盐、 甲基苯基次膦酸盐、 二 苯基次膦酸盐。
其他添加剂也包括无机填料,例如玻璃纤维,硼纤维,二氧化钛, 滑石粉, 云母, 钛酸钡, 玻璃微珠, 钛酸铜钙, 高岭土等。
本发明所述的树脂组合物以及使用该树脂组合物所制作成的制 件是电绝缘的, 表面电阻率不小于 1013 Ω。
另外, 本发明有必要提供树脂组合物的制备方法。
本发明所涉及的树脂组合物的制备方法如下:
称取物料: 按照以下重量百分比称取物料: 15_60wt%的热塑性塑 料或弹性体树脂基体; 30_70wt%的导热填料; 5_12wt%的激光敏感添 加剂; 0-15¾^/。的其他添加剂;
混合物料: 将树脂基体、 部分导热填料、 激光敏感添加剂、 其他 添加剂加入到高速混合机中, 混合均匀;
挤出成型: 混合均匀的物料从主喂料斗中进料, 剩余部分的导热 填料从侧喂料斗中进料, 采用普通双螺杆挤出机挤出, 冷却, 切粒, 得到树脂组合物的目标制件。
本发明所涉及的树脂组合物, 也可以通过如下的制备方法得到: 称取物料: 按照以下重量百分比称取物料: 15_60wt%的热固性塑 料或橡胶树脂基体; 30_70wt%的导热填料; 5-12¾^%的激光敏感添加 剂; 0_15¾^%的其他添加剂;
混合物料: 将树脂基体、 导热填料、 激光敏感添加剂、 其他添加 剂混合均匀;
热压成型:将所得到的树脂组合物装入合适的模具中,加热处理, 并采用压制成型法成型树脂组合物为目标制件。 本发明所述的树脂组合物具有优良的耐高温且导热性好,能够在 激光扫描过的区域内有选择性地沉积铜、镍、 金等金属, 可用于表面 贴装技术 (SMT) 的制件, 主要应用在电子电气零部件领域。 通过提 供具有激光直接成型 (LDS ) 特征的树脂组合物, 将该树脂组合物通 过注塑、挤出或者模压等成型工艺成型制件, 通过激光直接成型技术 在制件上形成电路, 然后直接将电子元件封装在电路上, 完全消除了 界面热阻, 从而实现高效散热。 如在 LED照明上的应用, 就可以实现 LED芯片无界面热阻封装, 同时将系统电路板、 散热器融为一体, 实 现高效散热, 延长 LED照明寿命。 附图说明
图 1为激光敏感添加剂结构示意图。 具体实施方式
本发明公开一种具有激光直接成型(Laser Direct Structuring) 功能的树脂组合物、制备所述树脂组合物的方法以及该树脂组合物的 应用。
所述树脂组合物由以下组分组成:
树脂基体 15-60wt%;
导热填料 30_70wt%;
激光敏感添加剂 5-12wt%; 以及
其他添加剂 0_15wt%;
其中激光敏感添加剂的化学通式为 XY204,等轴晶系,轴长 a=b=c, 轴角 α = β = Υ =90° ; 其中 X与 Υ均为金属元素, 来自元素周期表中 第 ΙΠΑ族、 I B族、 II B族、 VIB族、 VIIB族、 環族。 是一种重金属氧化物, 其中可包含铜、 锰、 铁、 锌、 镍、 铝、 钛、 钴、 镁、 锑、 锡的一种或多种的金属氧化物。一方面, 相对于树脂基体而 言, 它们都是热的良导体, 能够快速地将电子元件、 电子组件以及
LED灯所产生的热量扩散到环境当中去, 对提高组合物的导热能力有 协效作用。另一方面,本发明所选用的激光敏感添加剂的粒子直径小, 分布在 1. 5 μ m -2. 1 μ m, 比表面积大于 35000cm2/cm3。 其均匀分布在 大颗粒导热填料的间隙中, 可以有效地增加导热网络骨架的接触面 积, 形成众多的导热网络, 从而提高组合物的导热效率。
本发明所述树脂组合物的制备方法如下:
称取物料: 15_60^%的热塑性塑料, 或热固性塑料, 或橡胶, 或 弹性体树脂基体; 30_70wt%的导热填料; 5_12wt%的激光敏感添加剂; 0_15¾^%的其他添加剂;
混合物料: 将树脂基体、 导热填料、 激光敏感添加剂、 其他添加 剂加入到高速混合机中, 混合均匀;
将所得到的混合物料利用双螺杆挤出机挤出、冷却、切粒得到目 标产品; 或将所得到的混合物料装入模具中, 加热压制成型得到目标 制件。
本发明树脂组合物主要用来制作电子电气零部件, 包括电路基 材, 如电子元件、 电子组件的支架材料、 大功率 LED灯的底座或者电 路板。
在应用中,电子部件可通过 SMT方式悍接到 LDS工艺成型后的电 路基材上。不论采用哪种方式,电子部件和基材间都会存在界面热阻。 由于传统的基材(比如 PCB板) 的导热系数低, 电子部件所产生的热 量无法扩散到环境中去, 会严重地影响到组装后的产品的使用寿命, 特别是热敏感电子部件在持续的高温环境中工作, 性能损伤更加明 显。 如果存在界面热阻, 电子部件的散热效果会更差, 使用寿命会严 重縮短。
本发明所提供的树脂组合物具有高的导热系数,将电子部件直接 安装在通过 LDS工艺形成的电路上, 可明显地提高了散热效果。这是 因为电子元件直接封装在高导热系数的基材上便于散热; 另一方面, 此导电线路是通过无电化学镀工艺沉积在基材上的,导电线路和基材 构成了完美的整体, 不存在界面电阻, 导热效果会更好。
下面结合实施例和对比例对本发明具有激光直接成型功能的树 脂组合物、 制备方法、 效果以及用途作进一歩详细的描述, 但本发明 的实施方式不限于此。
以下实施例中选用的激光敏感添加剂有铜铬型激光敏感添加剂、 铜锰型激光敏感添加剂, 其结构如图 1所示。本发明所列举的铜锰型 添加剂是最优选择之一, 在激光制程、 以及无电化学镀过程中无有毒 金属离子产生, 在激光的作用下, 激光敏感添加剂的晶格被破坏, 里 面的金属元素会释放出来, 伴随有氧化还原反应。 比如, 铜铬型激光 敏感添加剂中的铬会由低价态变为高价态, 生成 Cr6+,是有毒离子。 铜锰型激光敏感添加剂中的锰同样由低价态变为高价态, 却是无毒 的, 这有利于环境友好。
实施例 1
树脂基体选用聚对苯二甲酰癸二胺 (PA10T, 来自金发科技股份 有限公司) 35wt%, 导热填料选用氮化硼 30¾^%和氧化镁 20wt%,铜锰 型激光敏感添加剂(来自巨发科技有限公司) 5wt%, 其他添加剂选用 纳米氧化铝 2wt%, 玻璃纤维 (来自巨石集团有限公司) 8wt%。
实施例 2
树脂基体选用聚对苯二甲酰癸二胺, 28wt%, 导热填料选用氮化 硼 30¾^/。和氧化镁 20wt%,铜锰型激光敏感添加剂 12wt%, 其他添加剂 选用纳米氧化铝 2wt%, 玻璃纤维 8wt%。
对比例 3
树脂基体选用聚对苯二甲酰癸二胺 40wt%, 导热填料选用氮化硼 30wtQ/ P氧化镁 20wt%,铜锰型激光敏感添加剂 Owt%,其他添加剂选用 纳米氧化铝 2wt%, 玻璃纤维 8wt%。
对比例 4
树脂基体选用聚对苯二甲酰癸二胺 37wt%, 导热填料选用氮化硼 30wtQ/ P氧化镁 20wt%,铜锰型激光敏感添加剂 3wt%,其他添加剂选用 纳米氧化铝 2wt%, 玻璃纤维 8wt%。
在实施例 1和 2, 对比例 3和 4中, 所选用的氮化硼为微观片状 结构, 平均粒径约为 150 μ πι, 直径与厚度比约为 20; 氮化镁为微观 球状结构, 平均粒径约为 20 μ πι; 纳米氧化铝为微观球状结构, 平均 粒径约为 20 μ πι; 铜锰型激光敏感添加剂的平均粒子直径为 1. 8士 0. 3 μ m, 比表面积大于 35000cm7cm3。 氮化硼属大粒径片状结构的导 热材料, 在树脂基体中主要起导热网络骨架作用, 小粒径球状结构的 氧化镁被氧化铝包覆, 均匀地分布在树脂基体中, 并且倾向于分布在 氮化硼的片状结构之间, 形成导热网络。
将上述各实施例中氧化镁加入到高速混合机中,再加入纳米氧化 铝继续混合均匀, 使纳米氧化铝均匀粘附于氧化镁的外层表面, 然后 和铜锰型激光敏感添加剂、聚对苯二甲酰癸二胺树脂混合均匀后, 从 双螺杆挤出机的主喂料斗进料。玻璃纤维从第一侧喂料口进料, 氮化 硼从第二侧喂料口进料, 挤出造粒, 得到一种具有导热功能的 LDS树 脂材料。
具有导热功能的 LDS树脂材料需要测试导热系数, 膜厚测试, 百 格测试 (Cross-Cut Test )。 导热系数的测试标准为 ISO 8301。 膜厚 测试, 即为测试 LDS材料在无电化学镀中沉积的金属薄膜厚度, 行业 内要求薄膜厚度分布在 7-12 μ πι内即为合格。百格测试, 即用美工刀 在金属薄膜上切割 100个 lmm*lmm的方格, 用 3M 610胶带黏贴后放 置约 2min后垂直拉起, 金属薄膜的脱落面积〈5%即为合格。 表面电 阻率的测试标准为 ASTM D257 o
测试结果如表 1所示。 当激光敏感添加剂的量少于 5wt%时, 在 激光的作用下, 释放出来的金属颗粒太少, 在无电化学镀过程中无法 实现镀铜、 镍、 金。 当添加量在 5-12%时, 在激光作用下释放出来足 够的金属颗粒, 并在无电化学镀的过程中起到活化中心的作用, 并能 顺利地镀铜、 镍、 金。 通过测试导热系数, 可以发现激光敏感添加剂 对热的传导还具有协效作用。 表 1测试结果
PA10T 激光敏感添加剂 导热填料 导热系数 膜厚测试 百格测试 wt% wt% wt% W/mK um 实 施
35 5 60 2. 45 7. 75 0K 例
1 实 施
28 12 60 2. 93 11. 68 0K 例
2 对 比
40 0 60 2. 31 0 NG 例
3 对 比
37 3 60 2. 40 0 NG 例
4 表 1中可知, 随着激光敏感添加剂的重量百分比的增加, 在导热 填料的重量百分比含量以及配比没有变化的情况下,导热系数逐歩增 加。可见,激光敏感添加剂有效地改善了 LDS树脂材料的热传导能力。 另外, 当激光敏感添加剂的用量低于 5«^%时 LDS特征并不明显, 百 格测试不合格。
实施例 5
聚苯硫醚(购自四川得阳化学有限公司) 17wt%,氮化硼 40wt%, 氧化镁 30wt%, 铜铬型激光敏感添加剂 5wt%, 纳米氧化铝 3wt%, 碳 纤维 5wt%。 加工方式和测试标准参考实施例 1。
测试结果表明, 此材料的导热系数为 3. 36 W/mK, 金属薄膜厚度 为 7. 68um, 百格测试金属薄膜脱落面积〈5%。
实施例 6
热致液晶聚合物 (来自金发科技股份有限公司) 58wt%, 氮化铝 10wt%,氧化锌 10wt%,铜铬型激光敏感添加剂 12wt%,碳纤维 10wt%。
所述液晶聚合物的熔点为 325 °C, 加工温度不高于 350°C, 氮化 铝为微观片状结构, 平均粒径约为 ΙΟΟ μ πι, 直径与厚度比约为 25 ; 所述氧化锌为微观球状结构, 平均粒径 15 μ πι。 铜铬型激光敏感添加 剂的平均粒子直径为 1. 8 ± 0. 3 μ m, 比表面积大于 35000cm2/cm3
加工方式和测试标准参照实施例 1。
测试结果表明, 此材料的导热系数为 1. 10 W/mK, 金属薄膜厚度 为 10. 55um, 百格测试金属薄膜脱落面积〈5%。
实施例 7
树脂基体选用聚酰胺 PA6 18wt%和聚丙烯树脂 PP 3wt%, 导热填 料为氮化硼 50wt%和石墨 20wt%, 铜锰型激光敏感添加剂 9wt%。 加入 氮化硼后,熔体的流动性变差。石墨在树脂基体中起到了润滑的作用, 降低了熔体的粘度, 有利于加工, 同时也提高了组合物的导热能力。
所选用的 PA6密度约为 1. 13g/cm3, 熔点 215°C, 加工温度不高 于 250°C ; 所选用的 PP为等规聚丙烯, 密度约为 1. 04 g/cm3, 加工 温度不高于 250°C ; 铜锰型激光敏感添加剂的平均粒子直径为 1. 8士 0. 3 μ m, 比表面积大于 35000cm2/cm3
将树脂基体同铜锰型激光敏感添加剂在高速混合机中混合均匀 后从双螺杆挤出机主喂料口加入, 氮化硼从第一侧喂料斗中加入, 石 墨从第二侧喂料斗中加入, 挤出, 冷却, 切粒得到树脂组合物。
测试标准参照实施例 1。
测试结果表明, 导热系数为 3. 47W/mK, 金属薄膜厚度为 9. 58um, 百格测试金属薄膜脱落面积〈5%。
实施例 8
双酚 A环氧树脂(Epoxy 828 )25wt%,氮化硼 45wt%,碳纤维 20wt%, 铜锰型激光敏感添加剂 5wt%, 酸酐固化剂 (MT-500TZ ) 4. 95wt%, 2- 乙基 -4-甲基咪唑 (2E4MZ ) 0. 05wt%o 将上述组分混合均匀后倒入模 具, 在热风烘箱中 100°C固化 2小时, 接着 130°C固化 3小时制备成 树脂组合物。
测试标准参照实施例 1。
测试结果表明, 导热系数为 2. 10W/mK, 金属薄膜厚度为 7. Hum, 百格测试金属薄膜脱落面积〈5%。
对比例 9
聚碳酸酯 (PC) 60. 2wt%, 碳化硅 15wt%, 球型石墨 10wt%, 铜 锰型激光敏感添加剂 4wt%, 磺酸盐阻燃剂 0. 3wt%, 滑石粉 0. 5wt%, 碳纤维 10wt%。
所选用的 PC加工温度在 240°C-280°C, 在 260°C/5KG下测试熔 融指数为 10-28g/10min, 铜锰型激光敏感添加剂的平均粒子直径为 1. 8 ± 0. 3 μ πι, 比表面积大于 35000cm2/cm3
加工方式和测试标准参照实施例 1。
测试结果表明, 此材料的导热系数为 0. 78 W/mK, 金属薄膜厚度 为 5. 73um, 百格测试金属薄膜脱落面积〉5%, 燃烧性能满足 UL 94 V_0 标准, 样条厚度为 1. 0mm。
实施例 5-8、 对比例 9的测试结果如表 2所示。 表 2 测试结果 激光敏感添加剂 导热填料 导热系数 膜厚测试 百格测试 wt% wt% W/mK um 实施例 5 6 70 3. 36 7. 68 0K 实施例 6 12 30 1. 10 10. 55 0K 实施例 7 9 70 3. 47 9. 58 0K 实施例 8 5 65 2. 10 7. 11 0K 对比例 9 4 25 0. 78 5. 73 NG
比重取值范围为 5-12 wt%, 导热填料的较佳比重取值范围为 30-70 wt%。
实施例 10
树脂基体选用耐高温聚酰胺 PA10T和脂肪族聚酰胺 PA66的组合 物, 其中 PA10T为 10wt%, PA66为 20wt%, 导热填料为氮化硼 30wt% 和氧化镁 20wt%, 铜锰激光敏感添加剂 10wt%, 其他添加剂选用无卤 阻燃剂为二甲基次膦酸铝 (购自科莱恩公司) 8wt%,勃姆石 2wt%。
双螺杆的加工温度分布在 290°C-330 °C。 将树脂基体、 勃姆石铜 锰型激光敏感添加剂在高速混合机中混合均匀后从双螺杆挤出机主 喂料口加入, 氮化硼从第一侧喂料斗中加入, 无卤阻燃剂从第二侧喂 料斗中加入, 挤出, 冷却, 切粒得到树脂组合物。
测试标准参考实施例 1。
测试结果表明, 导热系数为 1. 96W/mK, 金属薄膜厚度为 8. 39um, 百格测试金属薄膜脱落面积〈5%,在 1. Omm-3. 0mm厚度满足阻燃 UL 94
V-0等级。
从上述各实施例可知, 在树脂基体 15-60wt% ; 导热填料 30-70wt%; 激光敏感添加剂 5_12wt%; 以及其他添加剂 0_15wt%范围 时, 可通过膜厚测试以及百格测试, 且导热性能佳。
综上, 本发明所述的树脂组合物具有优良的耐高温且导热性好, 能够在激光扫描过的区域内有选择性地沉积铜、镍、 金等金属, 可用 于表面贴装技术 (SMT ) 的制件, 主要应用在电子电气零部件领域, 如 LED灯散热器。
以上所述仅为本发明的实施例, 并非因此限制本发明的专利范 围, 凡是利用本发明说明书内容所作的等效结构或等效流程变换, 或 直接或间接运用在其他相关的技术领域,均同理包括在本发明的专利 保护范围内。

Claims

1. 一种具有激光直接成型功能的树脂组合物, 由以下组分组成: 树脂基体 15_60wt%;
导热填料 30_70wt%;
激光敏感添加剂 5_12wt% ; 以及
其他添加剂 0_15wt%;
其中激光敏感添加剂的化学通式为 XY204, 等轴晶系, 轴长相等, 轴角相同均为 90° ; 其中 X与 Υ均为金属元素, 来自元素周期表中 第 ΙΠΑ族、 I B族、 Π Β族、 VIB族、 VIIB族、 環族。
2.根据权利要求 1所述的树脂组合物, 其特征在于: 所述 X金属 元素与所述 Y金属元素包括铬、 锰、 铁、 钴、 镍、 铜、 锌、 钯、 铝中 的一种或多种。
3.根据权利要求 1所述的树脂组合物, 其特征在于: 所述 X金属 元素与所述 Y金属元素选自于元素周期表中第四周期。
4.根据权利要求 1所述的树脂组合物, 其特征在于: 所述树脂基 体包括热塑性塑料、 热固性塑料、 橡胶和弹性体。
5.根据权利要求 4所述的树脂组合物, 其特征在于: 所述热塑性 塑料包括: 聚碳酸酯、 丙烯腈 -丁二烯-苯乙烯共聚物、 液晶聚合物、 聚酰胺、 聚苯硫醚、 聚苯醚、 聚砜、 聚芳酯、 聚醚醚酮、 聚醚酮酮、 聚醚醚酮酮、热塑性聚酰亚胺、聚縮醛、聚乙烯、聚丙烯、聚苯乙烯、 聚四氟乙烯、 聚丙烯酸酯类、 苯乙烯-丙烯腈共聚物、 聚对苯二甲酸 丁二醇酯、聚对苯二甲酸乙二醇酯、聚对苯二甲酸环己二醇酯中的一 种或多种的组合物。
6.根据权利要求 4所述的树脂组合物, 其特征在于: 所述热固性 塑料包括: 环氧树脂、 酚醛树脂、 不饱和聚酯、 聚酰亚胺中的一种或 多种的组合物。
7. 根据权利要求 4所述的树脂组合物, 其特征在于: 所述橡胶 包括天然橡胶和合成橡胶中的一种或多种的组合物。
8. 根据权利要求 4所述的树脂组合物, 其特征在于: 所述弹性 体包括苯乙烯类弹性体、 聚烯烃类弹性体、 聚酯弹性体、 聚酰胺弹性 体和聚氨酯弹性体中的一种或多种的组合物。
9.根据权利要求 1所述的树脂组合物, 其特征在于: 所述树脂组 合物表面电阻率不小于 1013 Ω。
10.根据权利要求 1所述的树脂组合物, 其特征在于: 所述激光 敏感添加剂的添加量为 5_9wt%。
11.根据权利要求 1-10 任意一项所述的树脂组合物, 其特征在 于: 所述导热填料包括: 氧化铝、氮化铝、氮化硅、氧化镁、碳化硅、 氮化硼、 碳纤维、 碳纳米管、 炭黑、 石墨、 氢氧化铝、 氧化锌、 氧化 镁、 氢氧化镁、 以及金属填料中的一种或多种。
12.根据权利要求 1 1所述的树脂组合物, 其特征在于: 所述导热 填料氮化硼为球状、 片状或纤维形式, 包括立方形氮化硼、 六方氮化 硼、 菱形氮化硼以及无定形氮化硼。
13.根据权利要求 1 1所述的树脂组合物, 其特征在于: 所述球状 结构导热填料的平均粒径在 10 μ πι-200 μ πι, 片状导热填料的径厚比 在 10-100, 纤维直径分布在 3-25 μ m。
14.根据权利要求 1-10 任意一项所述的树脂组合物, 其特征在 于: 所述其他添加剂包括无机填料, 无卤阻燃剂, 阻燃协效剂, 固化 剂, 脱模剂, 抗氧剂, 润滑剂的一种或多种。
15.根据权利要求 14所述的树脂组合物, 其特征在于: 所述树脂 基体为聚酰胺组合物, 其他添加剂中包括无卤阻燃剂, 无卤阻燃剂的 通式为
Figure imgf000024_0001
其中, Rl、 R2代表线型或支化的 1-6个碳原子的垸基和 /或芳基; R3代表线型或支化的 1-10个碳原子的亚垸基、 6-10个碳原子的 亚芳基、 垸基亚芳基或芳基亚垸基;
M代表元素周期表中第二和第三主族或副族中的金属离子; m为 2或 3; n为 1或 3; x为 1或 2。
16. 根据权利要求 14所述的树脂组合物, 其特征在于: 所述无 机填料包括玻璃纤维, 硼纤维, 二氧化钛, 滑石粉, 云母, 钛酸钡, 玻璃微珠, 钛酸铜钙, 高岭土中的一种或多种。
17. 根据权利要求 1-16 任意一项所述的树脂组合物的制备方 法, 包括以下歩骤:
称取物料: 15-60¾^%的热塑性塑料或弹性体基体; 30-70wt%的导 热填料; 5_12wt%的激光敏感添加剂; 0-15¾^/。的其他添加剂;
混合物料: 将热塑性塑料或弹性体基体、 部分导热填料、激光敏 感添加剂、 其他添加剂加入到高速混合机中, 混合均匀;
利用双螺杆挤出机挤出、 冷却、 切粒制得树脂组合物。
18.根据权利要求 17 所述的树脂组合物的制备方法, 其特征在 于: 所述挤出成型歩骤中, 将混合均匀的物料从挤出机的主喂料斗中 进料, 剩余部分的导热填料从侧喂料斗中进料, 采用双螺杆挤出机挤 出, 冷却, 切粒, 制得树脂组合物。
19.根据权利要求 1-16任意一项所述的树脂组合物的制备方法, 包括以下歩骤:
称取物料: 15_60wt%的热固性塑料或橡胶基体; 30_70wt%的导热 填料; 5_12wt%的激光敏感添加剂; 0-15¾^/。的其他添加剂;
混合物料: 将热固性塑料或橡胶基体、 导热填料、激光敏感添加 剂、 其他添加剂混合均匀;
将混合均匀的物料倒入合适的模具中, 加热, 压制成型。
20. 权利要求 1-16任意一项所述的树脂组合物用于制作电子电 气零部件的用途。
21.根据权利要求 20所述的树脂组合物, 其特征在于: 用于制作 LED灯散热器。
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