WO2023245621A1 - 一种绝缘胶膜、制备方法及其应用 - Google Patents
一种绝缘胶膜、制备方法及其应用 Download PDFInfo
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- WO2023245621A1 WO2023245621A1 PCT/CN2022/101123 CN2022101123W WO2023245621A1 WO 2023245621 A1 WO2023245621 A1 WO 2023245621A1 CN 2022101123 W CN2022101123 W CN 2022101123W WO 2023245621 A1 WO2023245621 A1 WO 2023245621A1
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- film
- epoxy resin
- carrier
- film material
- insulating adhesive
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/10—Adhesives in the form of films or foils without carriers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/40—Adhesives in the form of films or foils characterised by release liners
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/12—Mountings, e.g. non-detachable insulating substrates
- H01L23/14—Mountings, e.g. non-detachable insulating substrates characterised by the material or its electrical properties
Definitions
- the present invention belongs to the technical field of electronic packaging materials. More specifically, the present invention relates to an insulating adhesive film material used in semiconductor system-level packaging.
- the difference in thermal expansion coefficient between the epoxy resin insulating film and the carrier film can easily lead to bending or delamination of the carrier film and the dielectric film. That is, after the dielectric layer is dried or cured, the epoxy The resin insulating film is prone to bending or delamination with the substrate, thereby reducing the processability of the material.
- the object of the present invention is to provide a multifunctional insulating adhesive film material that can be used for semiconductor packaging and is suitable for the preparation of fine circuits by the additive method or the semi-additive method and its preparation method. application.
- the present invention adopts the following technical solutions.
- the glass transition temperature of the carrier film is ⁇ 80°C; preferably, the glass transition temperature is 80°C-120°C.
- the thermal expansion coefficient of the carrier film in the temperature range of 30 to 80°C is ⁇ 30 ppm/K, preferably 25 ppm/K or less, preferably 15 ppm/K or less, and more preferably 5 ppm/K or less.
- the surface of the carrier film is coated with a release agent, and the thickness of the release agent is 0.3 to 5 ⁇ m, preferably 0.5 to 4 ⁇ m, and more preferably 1 to 3 ⁇ m.
- the thickness of the dielectric film can be selected from 0.5 to 200 ⁇ m, preferably from 20 to 80 ⁇ m, and more preferably from 30 to 50 ⁇ m.
- the epoxy resin is selected from bisphenol A type epoxy resin, bisphenol F type epoxy resin, phenolic epoxy resin, o-cresol type epoxy resin, multifunctional epoxy resin, alicyclic ring Oxygen resin, resorcinol epoxy resin, rubber modified epoxy resin, polyurethane modified epoxy resin, biphenyl epoxy resin, dicyclopentadiene epoxy resin, brominated epoxy resin;
- the bisphenol A Type epoxy resin is selected from Nanya NPEL-128, NPEL-127, NPEL-144, NPES-609, NPES-901, NPES-902, NPES-903, NPES-904, NPES-907, NPES-909, such as Guodu Chemical YD-001, YD-012, YD-013k, YD-014, YD-134, YD-134D, YD-134L, YD-136, YD-128, YD-127, produced by Huntsman GY 2600, GY 6010, GY 60
- the amount of curing agent added is based on the ratio of the sum of amino equivalents, hydroxyl equivalents, phenolic hydroxyl equivalents, carboxyl equivalents, acid anhydride equivalents, cyano equivalents, ester equivalents and epoxy equivalents to 0.01 to 1.2.
- the solvent used in the electronic slurry for the dielectric film of the present invention is a volatile solvent, selected from aromatic solvents, halogenated hydrocarbons, aliphatic hydrocarbons, alicyclic hydrocarbons, alcohols, ketones, esters, and amides.
- the raw materials of the dielectric film electronic slurry also include a modifier, the modifier is selected from a diisocyanate compound, and the diisocyanate compound is selected from the group consisting of hydrogenated diphenylmethane diisocyanate, isophorone diisocyanate, Toluene diisocyanate, diphenylmethane diisocyanate, dicyclohexylmethane diisocyanate, hexamethylene diisocyanate, lysine diisocyanate.
- the modifier is selected from a diisocyanate compound
- the diisocyanate compound is selected from the group consisting of hydrogenated diphenylmethane diisocyanate, isophorone diisocyanate, Toluene diisocyanate, diphenylmethane diisocyanate, dicyclohexylmethane diisocyanate, hexamethylene diisocyanate, lysine diisocyanate.
- the mixing method of the electronic slurry includes one or more combinations of stirring, ball milling, sand milling, ultrasonic, etc.
- the coating method of the electronic paste is selected from gravure printing, microgravure printing, comma doctor blade, and slit extrusion.
- the semiconductor electronic packaging material is a packaging substrate, a packaging carrier, a fan-out type board level packaging and rewiring. Material.
- the present invention has found that the carrier layer and the insulating film material bend after drying or curing, which is related to the delamination of the substrate. This invention further suppresses the drying or curing of the insulating film material by controlling the glass transition temperature and thermal expansion coefficient of the carrier layer. Later, the phenomenon of bending and delamination with the substrate occurs, thereby enabling the manufacture of fine electronic circuits.
- Figure 1 is a schematic structural diagram of the insulating film material, in which 1-1 is the carrier film material, 1-2 is the dielectric film 2, and 1-3 is the cover film material.
- This embodiment provides a dielectric layer suitable for semiconductor electronic packaging fields such as packaging substrates, packaging carriers, fan-out board-level packaging and rewiring, thereby developing an insulating adhesive film material with excellent processability and a preparation method thereof. , solve the problem of curling or delamination of insulating adhesive film materials due to mismatch of thermal expansion coefficient and dielectric film during the drying and curing process, so as to adapt to the requirements for adhesive film materials in application fields such as packaging substrates.
- the insulating adhesive film material is composed of a carrier film, a dielectric film and a cover film, wherein the dielectric film is located between the carrier film and the cover film to form a sandwich structure;
- the glass transition temperature of the carrier film is ⁇ 80°C; preferably, the glass transition temperature is 80°C-120°C.
- the thermal curing process temperature of the adhesive film material is significantly higher than This temperature will cause serious deformation of the carrier film and affect device processing.
- the test method for the glass transition temperature of the carrier film is the TMA tensile test method.
- the surface of the carrier film is coated with a release agent, and the thickness of the release agent is 0.3 to 5 ⁇ m, preferably 0.5 to 4 ⁇ m, and more preferably 1 to 3 ⁇ m.
- the thickness of the release agent is less than 0.3 ⁇ m, the adhesive film material cannot achieve good separation from the carrier film after thermal curing.
- the thickness of the release agent is higher than 5 ⁇ m, holes and lack of glue are likely to occur during the processing of the dielectric layer of the adhesive film material, reducing the consistency and uniformity of the material.
- the dielectric film is made of electronic slurry, which contains epoxy resin, curing agent, filler and solvent.
- the electronic slurry also contains a modifier, and the modifier is selected from a diisocyanate compound.
- the diisocyanate compound is selected from the group consisting of hydrogenated diphenylmethane diisocyanate, isophorone diisocyanate, toluene diisocyanate, and diphenyl diisocyanate. Methane diisocyanate, dicyclohexylmethane diisocyanate, hexamethylene diisocyanate, lysine diisocyanate.
- the preparation method of the dielectric film is to mix epoxy resin, filler, curing agent and solvent into electronic slurry, let it stand for 1 hour to remove air bubbles, and use a coater to apply the film.
- the thickness of the dielectric film can be selected from 0.5 to 200 ⁇ m, preferably from 20 to 80 ⁇ m, and more preferably from 30 to 50 ⁇ m.
- the filler content is 5 to 95 wt%, preferably 20 to 80 wt%, and more preferably 50 to 75 wt%.
- the epoxy resin is selected from the group consisting of bisphenol A-type epoxy resin, bisphenol F-type epoxy resin, novolac-type epoxy resin, o-cresol-type epoxy resin, and multifunctional epoxy resin. , Alicyclic epoxy resin, resorcinol epoxy resin, rubber modified epoxy resin, polyurethane modified epoxy resin, biphenyl epoxy resin, dicyclopentadiene epoxy resin, brominated epoxy resin;
- the bisphenol A type epoxy resin is selected from Nanya NPEL-128, NPEL-127, NPEL-144, NPES-609, NPES-901, NPES-902, NPES-903, NPES-904, NPES-907, NPES- 909.
- YD-001, YD-012, YD-013k, YD-014, YD-134, YD-134D, YD-134L, YD-136, YD-128, YD-127 produced by Huntsman GY 2600, GY 6010, GY 6020, MY 790-1 ⁇ LY 1556, GY 507, etc.
- bisphenol F epoxy resin is selected from NPEF-170 produced by Nanya, EPALLOY 8220, EPALLOY 8220E, EPALLOY 8230 produced by CVC, and EPALLOY 8230 produced by Huntsman GY 281, GY 282, GY 285, PY 306, PY 302-2 ⁇ PY 313, etc.
- the phenolic epoxy resin is selected from NPPN-638S, NPPN-631 produced by Nanya, EPALLOY 8240, EPALLOY 8240, EPALLOY 8250, EPALLOY 8330 produced by CVC, etc.
- NPCN-701, NPCN-702, NPCN-703, NPCN-704, NPCN-704L, NPCN-704K80, etc. multifunctional epoxy resins are selected from NPPN-431A70 produced by Nanya, ERISYS GA-240 produced by CVC, etc., alicyclic
- the family epoxy resin is selected from EPALLOY 5000, EPALLOY 5200, JE-8421, etc. produced by CVC, and the resorcinol epoxy resin is selected from ERISYS RDGE produced by CVC, and rubber modified epoxy resin HyPox RA 95 and HyPox RA produced by CVC.
- HyPox RA 1340, HyPox RF 928, HyPox RM 20, HyPox RM 22, HyPox RK 84L, HyPox RK 820, etc. polyurethane modified epoxy resin, biphenyl epoxy resin are selected from YX4000, YX4000K, etc. produced by Mitsui Chemicals in Japan.
- YX4000H, YX4000HK, YL6121H, YL6121HN; dicyclopentadiene epoxy resin and brominated epoxy resin are selected from CYDB-500, CYDB-700, CYDB-900, CYDB-400, CYDB-450A80 produced by Yueyang Baling Petrochemical, etc. of one or more.
- the curing agent is a compound whose molecular structure contains one or more of amino group, hydroxyl group, phenolic hydroxyl group, carboxyl group, acid anhydride, cyano group, ester group, etc., which can react with epoxy group.
- the curing agent is selected from benzophenone tetracarboxylic dianhydride, glutaric anhydride, dicyandiamine, 9,9'-spirobis[9H-fluorene]-2,2'-diamine, diaminodiphenyl sulfone, ethanol Diamine, triethylenetetramine, 4,4-diaminodiphenylmethane, polyamide, methylnadic anhydride, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, methyltetrahydrophthalic anhydride, methylhexahydrophthalic anhydride, dodecane Alkenyl succinic anhydride, N-dodecyl succinic anhydride, octenyl succinic anhydride, phenyl succinic anhydride, 2,3-nedicarboxylic anhydride, 2-methylimidazole, 2-methyl-4-ethyl Imidazo
- the amount of curing agent added is based on the ratio of the sum of amino equivalents, hydroxyl equivalents, phenolic hydroxyl equivalents, carboxyl equivalents, acid anhydride equivalents, cyano equivalents, ester equivalents and epoxy equivalents to 0.01 to 1.2.
- the filler particles are selected from silica, and the size of the filler particles ranges from 20 nm to 10 ⁇ m, preferably from 50 nm to 5 ⁇ m, and more preferably from 200 nm to 1 ⁇ m.
- the filler particles account for 5 wt% to 95 wt% of the solid content of the electronic slurry, that is, the mass excluding volatile components such as solvents.
- the solvent is a volatile solvent, selected from aromatic solvents, halogenated hydrocarbons, aliphatic hydrocarbons, alicyclic hydrocarbons, alcohols, ketones, esters, and amides; the aromatic solvent Selected from xylene, o-xylene, meta-xylene, p-xylene, hexamethylbenzene, ethylbenzene, etc.; halogenated hydrocarbons are selected from chlorobenzene, dichlorobenzene, dichloromethane, etc.; aliphatic hydrocarbons are selected from pentane , hexane, octane, etc.; alicyclic hydrocarbons are selected from cyclohexane, cyclohexanone, toluene, etc.; alcohols are selected from methanol, ethanol, isopropanol, etc.; esters are selected from methyl acetate, acetic acid Ethyl ester, propy
- the cover film material is selected from polymer film materials and paper-based film materials
- the polymer film material is selected from biaxially oriented polypropylene film (BOPP), polyester film (PET), polyether film Etherketone film (PEEK), polyetherimide film (PEI), polyimide film (PI), polycarbonate film (PC);
- the paper base film material is selected from release paper and laminated paper.
- the thickness of the cover film material is 1 ⁇ m to 80 ⁇ m, preferably 5 ⁇ m to 60 ⁇ m, and more preferably 10 ⁇ m to 30 ⁇ m.
- the carrier film material is preferably a plastic film with a light transmittance of ⁇ 95%, such as polyester film (PET), polypropylene film (PP), polyimide film (PI), polyethylene film ( One of PE), polyvinyl chloride film (PVC), polyether ether ketone film (PEEK), polycarbonate film (PC), ethylene film (PS), etc.
- a plastic film with a light transmittance of ⁇ 95% such as polyester film (PET), polypropylene film (PP), polyimide film (PI), polyethylene film ( One of PE), polyvinyl chloride film (PVC), polyether ether ketone film (PEEK), polycarbonate film (PC), ethylene film (PS), etc.
- the light transmittance of the carrier film is lower than 95%, the use of adhesive film materials to manufacture devices affects the precision of laser drilling, resulting in low roundness and low verticality of the drilled holes.
- Another aspect of the present invention provides a method for preparing the above-mentioned insulating film material, which includes the following steps:
- the raw materials of the dielectric film electronic slurry include epoxy resin, fillers, curing agents and solvents.
- the raw materials of the dielectric film electronic slurry also include a modifier, the modifier is selected from a diisocyanate compound, and the diisocyanate compound is selected from the group consisting of hydrogenated diphenylmethane diisocyanate, isoflurane Ertone diisocyanate, toluene diisocyanate, diphenylmethane diisocyanate, dicyclohexylmethane diisocyanate, hexamethylene diisocyanate, lysine diisocyanate.
- the modifier is selected from a diisocyanate compound
- the diisocyanate compound is selected from the group consisting of hydrogenated diphenylmethane diisocyanate, isoflurane Ertone diisocyanate, toluene diisocyanate, diphenylmethane diisocyanate, dicyclohexylmethane diisocyanate, hexamethylene diisocyanate, lysine diis
- the mixing method of the electronic slurry includes one or more combinations of stirring, ball milling, sand milling, ultrasonic, etc.
- the coating method of the electronic paste is selected from gravure printing, microgravure printing, comma doctor blade, and slit extrusion.
- drying temperature is 50°C to 150°C.
- the bonding temperature is room temperature to 150°C
- the bonding method is hot pressing bonding.
- Use formula A as the electronic slurry in the dielectric film and apply it on a PET release film with a thermal expansion coefficient of 50 ppm/K, Tg of 65°C, and a release agent thickness of 2 ⁇ m as a carrier film.
- the thickness of the dielectric film is 23 ⁇ m, and then dried at 60°C for 5 minutes. After drying and taking it out, it was found that the carrier film and the medium were bent, and the next step of lamination with BOPP could not be carried out, seriously affecting the reliability of the components.
- Use formula C as the electronic slurry in the dielectric film and apply it on a PET release film with a thermal expansion coefficient of 36ppm/K, Tg of 75°C, and a release agent thickness of 1.5 ⁇ m as a carrier film.
- the thickness of the dielectric film is 25 ⁇ m, and then dried at 60°C for 5 minutes. After drying, take it out and heat-press the insulating polymer composite film and the BOPP film with a thickness of 20 ⁇ m. During the hot-pressing process, the temperature of the heating roller is set to 80°C and the heating pressure is 5kg. After hot pressing, an insulating film material with a three-layer structure is obtained. Finally, cure at 100°C for 30 minutes and 180°C for 90 minutes. After taking out the cured insulating film material, it was found that the carrier film and the dielectric layer were separated, which led to a reduction in the reliability of the insulating film material, thereby affecting the performance and reliability of the components.
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- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
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Abstract
本发明公开一种绝缘胶膜、制备方法及其应用,具体公开了绝缘胶膜材料由下层载体膜、中间层介质膜以及上层覆盖膜三层结构组成,其中所述载体膜的玻璃化转变温度为80℃以上;且所述载体膜在30~80℃温度区间的热膨胀系数为30ppm/K以下;且所述载体膜表面涂覆有离型剂。本发明绝缘胶膜在烘干或固化后,不会发生卷曲或出现载体膜与基板分层的现象,从而得到具有高稳定性、高可靠性的绝缘胶膜材料。
Description
本发明属于电子封装材料技术领域,更具体地,本发明涉及一种应用于半导体系统级封装用的绝缘胶膜材料。
随着电子信息技术的高速发展,特别是近年以来以智能手机、微型电脑、智能可穿戴等设备为主技术的快速流行,对其中电子系统的小型化、轻薄化、多功能、高性能等方面提出了越来越高的要求,尤其是对HDI基板、FCBGA、IC封装载板的需求量与日俱增。环氧树脂基复合材料以其优异的粘结性、可加工性强、各项性能易于调整等特征,相比其他聚合物基复合材料具有更多的应用。
但是环氧树脂绝缘胶膜在烘干和固化过程中因与载体膜热膨胀系数之间的差异容易导致弯曲或者载体膜与介质膜分层的现象,即介质层在烘干或者固化后,环氧树脂绝缘胶膜容易发生弯曲或者与基板出现分层的现象,从而降低材料的可加工性。
发明内容
针对此问题,经过细致的研究,找到了一种制备绝缘胶膜材料的方法。在烘干或固化后,绝缘胶膜材料不会发生卷曲或出现载体膜与基板分层的现象,从而得到具有高稳定性、高可靠性的绝缘胶膜材料。
为了解决上述背景技术中所提出的问题,本发明的目的在于提供一种可用于半导体封装的、适用于加成法或半加成法制备精细线路的多功能绝缘胶膜材料及其制备方法和应用。
为了实现上述发明目的,本发明采取了以下技术方案。
本发明一个方面提供了一种绝缘胶膜材料,绝缘胶膜材料由载体膜、介质膜和覆盖膜组成,其中介质膜位于载体膜和覆盖膜中间形成三明治结构;
所述载体膜的玻璃化转变温度≥80℃;优选地,玻璃化转变温度80℃-120℃。
载体膜在30~80℃温度区间的热膨胀系数≤30ppm/K,优选为25ppm/K以下,优选为15ppm/K以下,更优选为5ppm/K以下。
载体膜表面涂覆有离型剂,离型剂的厚度为0.3~5μm,优选为0.5~4μm,更优选为1~3μm。
所述介质膜由电子浆料制成,所述电子浆料中包含环氧树脂、固化剂、填料和溶剂。所述电子浆料中还包含改性剂,所述改性剂选自二异氰酸酯化合物,所述二异氰酸酯化合物选自氢化二苯甲烷二异氰酸酯、异氟尔酮二异氰酸酯、甲苯二异氰酸酯、二苯基甲烷二异氰酸酯、二环己基甲烷二异氰酸酯、六亚甲基二异氰酸酯、赖氨酸二异氰酸酯。
所述介质膜的制备方法为将环氧树脂、填料、固化剂和溶剂混合成电子浆料,静置1h除去气泡,使用涂布机进行涂膜。
介质膜的厚度可选择为0.5~200μm,优选为20~80μm,更优选为30~50μm。
其中,填料的含量为5~95wt%,优选为20~80wt%,更优选为50~75wt%。
进一步地,所述环氧树脂选自双酚A型环氧树脂、双酚F型环氧树脂、酚醛型环氧树脂、邻甲酚醛型环氧树脂、多官能团环氧树脂、脂环族环氧树脂、间苯二酚环氧树脂、橡胶改性环氧树脂、聚氨酯改性环氧树脂、联苯环氧树脂、双环戊二烯环氧树脂、溴化环氧树脂;所述双酚A型环氧树脂选自南亚NPEL-128、NPEL-127、NPEL-144、NPES-609、NPES-901、NPES-902、NPES-903、NPES-904、NPES-907、NPES-909、如国都化工YD-001、YD-012、YD-013k、YD-014、YD-134、YD-134D、YD-134L、YD-136、YD-128、YD-127,亨斯迈生产的
GY 2600、
GY 6010、
GY 6020、
MY 790-1、
LY 1556、
GY 507等,双酚F型环氧树脂选自如南亚生产的NPEF-170、CVC生产的EPALLOY 8220、EPALLOY 8220E、EPALLOY 8230,亨斯迈生产的
GY 281、
GY 282、
GY 285、
PY 306、
PY 302-2、
PY 313等,酚醛型环氧树脂选自如南亚生产的NPPN-638S、NPPN-631、CVC生产的EPALLOY 8240、EPALLOY 8240、EPALLOY 8250、EPALLOY 8330等,邻甲酚醛型环氧树脂选自如南亚生产的NPCN-701、NPCN-702、NPCN-703、NPCN-704、NPCN-704L、NPCN-704K80等,多官能团环氧树脂选自如南亚生产的NPPN-431A70、CVC生产的ERISYS GA-240等,脂环族环氧树脂选自如CVC生产的EPALLOY 5000、EPALLOY 5200、JE-8421等,间苯二酚环氧树脂选自如CVC生产的ERISYS RDGE、橡胶改性环氧树脂CVC生产的HyPox RA 95、HyPox RA 840、HyPox RA 1340、HyPox RF 928、HyPox RM 20、HyPox RM 22、HyPox RK 84L、 HyPox RK 820等,聚氨酯改性环氧树脂、联苯环氧树脂选自如日本三井化学生产的YX4000、YX4000K、YX4000H、YX4000HK、YL6121H、YL6121HN;双环戊二烯环氧树脂、溴化环氧树脂选自如岳阳巴陵石化生产的CYDB-500、CYDB-700、CYDB-900、CYDB-400、CYDB-450A80等中的一种或多种。
其中,固化剂为分子结构中含有能够与环氧基发生反应的氨基、羟基、酚羟基、羧基、酸酐、氰基、酯基等中的一种或多种的化合物。固化剂选自苯酮四羧酸二酐、戊二酸酐、二氰二胺、9,9'-螺二[9H-芴]-2,2'-二胺、二氨基二苯基砜、乙二胺、三乙烯四胺、4,4-二氨基二苯基甲烷、聚酰胺、甲基纳迪克酸酐、四氢苯酐、六氢苯酐、甲基四氢苯酐、甲基六氢苯酐、十二烯基丁二酸酐、N-十二烷基丁二酸酐、辛烯基酸酐、苯基丁二酸酐、2,3-奈二甲酸酐、2-甲基咪唑、2-甲基-4-乙基咪唑,十一烷基咪唑、十七烷基咪唑、2-苯基咪唑、2-苯基-4-甲基咪唑、2,4,6-三(二甲胺基甲基)酚、苯胺甲醛树脂、活性酯、酸酐改性聚丁二烯、苯酚甲醛树脂、线性酚醛树脂等中的一种或多种。固化剂的添加量以氨基当量、羟基当量、酚羟基当量、羧基当量、酸酐当量、氰基当量、酯基当量之和与环氧当量的比例为0.01~1.2为基础进行添加。
其中,填料粒子选自二氧化硅,其中填料粒子的尺寸为20nm~10μm,优选为50nm~5μm,更优选为200nm~1μm。填料粒子占电子浆料中固体成分即不含溶剂等挥发成分的质量的5wt%~95wt%。
本发明用于介质膜的电子浆料所使需用的溶剂为可挥发溶剂,选自芳香类溶剂、卤化烃类、脂肪烃类、脂环烃类、醇类、酮类、酯类、酰胺类;所述芳香类溶剂选自二甲苯、邻二甲苯、间二甲苯、对二甲苯、六甲基苯、乙苯等;卤化烃类选自氯苯、二氯苯、二氯甲烷等;脂肪烃类选自戊烷、己烷、辛烷等;脂环烃类选自环己烷、环己酮、甲苯环己酮等;醇类选自甲醇、乙醇、异丙醇等;酯类选自醋酸甲酯、醋酸乙酯、醋酸丙酯等;酮类选自丙酮、2-丁酮、甲基异丁基甲酮等;酰胺选自二甲基甲酰胺、六甲基磷酰胺,N-甲基甲酰胺、二甲基乙酰胺等中的一种或多种。
覆盖膜材料选自聚合物薄膜材料、纸基膜材料,所述聚合物薄膜材料选自双向拉伸聚丙烯薄膜(BOPP)、聚酯薄膜(PET)、聚醚醚酮薄膜(PEEK)、聚醚酰亚胺薄膜(PEI)、聚酰亚胺薄膜(PI)、聚碳酸酯薄膜(PC);纸基膜材料选自离型纸、淋膜纸。覆盖膜材料的厚度为1μm~80μm,优选为5μm~60μm,更优选为10μm~30μm。
其中,载体膜材料优选透光率≥95%的塑料薄膜,如聚酯薄膜(PET)、聚丙烯薄膜(PP)、 聚酰亚胺薄膜(PI)、聚乙烯薄膜(PE)、聚氯乙烯薄膜(PVC)、聚醚醚酮薄膜(PEEK)、聚碳酸酯薄膜(PC)、乙烯薄膜(PS)等中的一种。
本发明另一个方面提供了一种上述绝缘胶膜材料的制备方法,其包括以下步骤:
S1)将制备介质膜电子浆料的原料进行混合,获得介质膜的电子浆料;
S2)将介质膜的电子浆料涂覆在载体膜表面,并干燥获得负载介质膜的载体膜;
S3)将覆盖膜覆盖在介质膜表面进行贴合,得到绝缘胶膜材料。
进一步地,所述介质膜电子浆料的原料包括环氧树脂、填料、固化剂和溶剂。
进一步地,所述介质膜电子浆料的原料还包括改性剂,所述改性剂选自二异氰酸酯化合物,所述二异氰酸酯化合物选自氢化二苯甲烷二异氰酸酯、异氟尔酮二异氰酸酯、甲苯二异氰酸酯、二苯基甲烷二异氰酸酯、二环己基甲烷二异氰酸酯、六亚甲基二异氰酸酯、赖氨酸二异氰酸酯。
进一步地,电子浆料的混合方法包括搅拌、球磨、砂磨、超声等中的一种或多种组合使用。
进一步地,电子浆料的涂覆方式选自凹版印刷、微凹版印刷、逗号刮刀、狭缝挤出。
进一步地,干燥的温度为50℃~150℃。
进一步地,贴合温度为室温至150℃,贴合的方法为热压贴合。
本发明又一个方面提供了上述任一绝缘胶膜材料作为半导体电子封装材料中的电介质层中的用途,所述半导体电子封装材料为封装基板、封装载板、扇出型板级封装再布线的材料。
本发明发现了载体层与绝缘胶膜材料烘干或固化后出现弯曲以及与基板分层有关,本进一步通过控制载体层的玻璃化转变温度和热膨胀系数,抑制了绝缘胶膜材料烘干或固化后出现弯曲以及与基板分层的现象,从而实现精细电子线路的制造。
图1为绝缘胶膜材料的结构示意图,其中1-1为载体膜材料,1-2为介质膜2,1-3为覆盖膜材料。
为了使本发明的上述目的、特征和优点能够更加明显易懂,下面结合附图对本发明的具体实施方式做详细的说明,但不能理解为对本发明的可实施范围的限定。
本实施例提供了一种适用于封装基板、封装载板、扇出型板级封装再布线等半导体电子封装领域中的电介质层,从而开发出可加工性优异的绝缘胶膜材料及其制备方法,解决在绝缘胶膜材料在烘干和固化过程由于热膨胀系数与介质膜不匹配出现卷曲或分层问题,以适应封装基板等应用领域对胶膜材料的要求。
本发明一个方面提供了一种绝缘胶膜材料,绝缘胶膜材料由载体膜、介质膜和覆盖膜组成,其中介质膜位于载体膜和覆盖膜中间形成三明治结构;
所述载体膜的玻璃化转变温度≥80℃;优选地,玻璃化转变温度80℃-120℃,当载体膜的玻璃化转变温度低于80℃时,胶膜材料热固化过程温度大幅高于此温度,将导致载体膜严重变形,影响器件加工。载体膜的玻璃化转变温度的测试方法为采用TMA拉伸测试方法。
载体膜在30~80℃温度区间的热膨胀系数≤30ppm/K,优选为25ppm/K以下,更优选为5-20ppm/K。因为较低的热膨胀系数使得离型膜在受热时,发生形变越小,对绝缘胶膜的影响越小。当载体膜的热膨胀系数大于30ppm/K时,绝缘胶膜材料在烘干或固化后,会发生卷曲或出现载体膜与基板分层的现象。
载体膜表面涂覆有离型剂,离型剂的厚度为0.3~5μm,优选为0.5~4μm,更优选为1~3μm。当离型剂厚度低于0.3μm时,胶膜材料经过热固化后无法实现与载体膜的良好分离。当离型剂厚度高于5μm,胶膜材料介质层加工过程易出现孔洞缺胶现象,降低材料的一致性和均一性。
所述介质膜由电子浆料制成,所述电子浆料中包含环氧树脂、固化剂、填料和溶剂。所述电子浆料中还包含改性剂,所述改性剂选自二异氰酸酯化合物,所述二异氰酸酯化合物选自氢化二苯甲烷二异氰酸酯、异氟尔酮二异氰酸酯、甲苯二异氰酸酯、二苯基甲烷二异氰酸酯、二环己基甲烷二异氰酸酯、六亚甲基二异氰酸酯、赖氨酸二异氰酸酯。
所述介质膜的制备方法为将环氧树脂、填料、固化剂和溶剂混合成电子浆料,静置1h除去气泡,使用涂布机进行涂膜。
介质膜的厚度可选择为0.5~200μm,优选为20~80μm,更优选为30~50μm。
其中,填料的含量为5~95wt%,优选为20~80wt%,更优选为50~75wt%。
在一些具体的实施例中,所述环氧树脂选自双酚A型环氧树脂、双酚F型环氧树脂、酚醛型环氧树脂、邻甲酚醛型环氧树脂、多官能团环氧树脂、脂环族环氧树脂、间苯二酚环氧树脂、橡胶改性环氧树脂、聚氨酯改性环氧树脂、联苯环氧树脂、双环戊二烯环氧树脂、溴化环氧树脂;所述双酚A型环氧树脂选自南亚NPEL-128、NPEL-127、NPEL-144、NPES-609、 NPES-901、NPES-902、NPES-903、NPES-904、NPES-907、NPES-909、如国都化工YD-001、YD-012、YD-013k、YD-014、YD-134、YD-134D、YD-134L、YD-136、YD-128、YD-127,亨斯迈生产的
GY 2600、
GY 6010、
GY 6020、
MY 790-1、
LY 1556、
GY 507等,双酚F型环氧树脂选自如南亚生产的NPEF-170、CVC生产的EPALLOY 8220、EPALLOY 8220E、EPALLOY 8230,亨斯迈生产的
GY 281、
GY 282、
GY 285、
PY 306、
PY 302-2、
PY 313等,酚醛型环氧树脂选自如南亚生产的NPPN-638S、NPPN-631、CVC生产的EPALLOY 8240、EPALLOY 8240、EPALLOY 8250、EPALLOY 8330等,邻甲酚醛型环氧树脂选自如南亚生产的NPCN-701、NPCN-702、NPCN-703、NPCN-704、NPCN-704L、NPCN-704K80等,多官能团环氧树脂选自如南亚生产的NPPN-431A70、CVC生产的ERISYS GA-240等,脂环族环氧树脂选自如CVC生产的EPALLOY 5000、EPALLOY 5200、JE-8421等,间苯二酚环氧树脂选自如CVC生产的ERISYS RDGE、橡胶改性环氧树脂CVC生产的HyPox RA 95、HyPox RA 840、HyPox RA 1340、HyPox RF 928、HyPox RM 20、HyPox RM 22、HyPox RK 84L、HyPox RK 820等,聚氨酯改性环氧树脂、联苯环氧树脂选自如日本三井化学生产的YX4000、YX4000K、YX4000H、YX4000HK、YL6121H、YL6121HN;双环戊二烯环氧树脂、溴化环氧树脂选自如岳阳巴陵石化生产的CYDB-500、CYDB-700、CYDB-900、CYDB-400、CYDB-450A80等中的一种或多种。
在一些具体的实施例中,固化剂为分子结构中含有能够与环氧基发生反应的氨基、羟基、酚羟基、羧基、酸酐、氰基、酯基等中的一种或多种的化合物。固化剂选自苯酮四羧酸二酐、戊二酸酐、二氰二胺、9,9'-螺二[9H-芴]-2,2'-二胺、二氨基二苯基砜、乙二胺、三乙烯四胺、4,4-二氨基二苯基甲烷、聚酰胺、甲基纳迪克酸酐、四氢苯酐、六氢苯酐、甲基四氢苯酐、甲基六氢苯酐、十二烯基丁二酸酐、N-十二烷基丁二酸酐、辛烯基酸酐、苯基丁二酸酐、2,3-奈二甲酸酐、2-甲基咪唑、2-甲基-4-乙基咪唑,十一烷基咪唑、十七烷基咪唑、2-苯基咪唑、2-苯基-4-甲基咪唑、2,4,6-三(二甲胺基甲基)酚、苯胺甲醛树脂、活性酯、酸酐改性聚丁二烯、苯酚甲醛树脂、线性酚醛树脂等中的一种或多种。固化剂的添加量以氨基当量、羟基当 量、酚羟基当量、羧基当量、酸酐当量、氰基当量、酯基当量之和与环氧当量的比例为0.01~1.2为基础进行添加。
在一些具体的实施例中,填料粒子选自二氧化硅,其中填料粒子的尺寸为20nm~10μm,优选为50nm~5μm,更优选为200nm~1μm。填料粒子占电子浆料中固体成分即不含溶剂等挥发成分的质量的5wt%~95wt%。
在一些具体的实施例中,溶剂为可挥发溶剂,选自芳香类溶剂、卤化烃类、脂肪烃类、脂环烃类、醇类、酮类、酯类、酰胺类;所述芳香类溶剂选自二甲苯、邻二甲苯、间二甲苯、对二甲苯、六甲基苯、乙苯等;卤化烃类选自氯苯、二氯苯、二氯甲烷等;脂肪烃类选自戊烷、己烷、辛烷等;脂环烃类选自环己烷、环己酮、甲苯环己酮等;醇类选自甲醇、乙醇、异丙醇等;酯类选自醋酸甲酯、醋酸乙酯、醋酸丙酯等;酮类选自丙酮、2-丁酮、甲基异丁基甲酮等;酰胺选自二甲基甲酰胺、六甲基磷酰胺,N-甲基甲酰胺、二甲基乙酰胺等中的一种或多种。
在一些具体的实施例中,覆盖膜材料选自聚合物薄膜材料、纸基膜材料,所述聚合物薄膜材料选自双向拉伸聚丙烯薄膜(BOPP)、聚酯薄膜(PET)、聚醚醚酮薄膜(PEEK)、聚醚酰亚胺薄膜(PEI)、聚酰亚胺薄膜(PI)、聚碳酸酯薄膜(PC);纸基膜材料选自离型纸、淋膜纸。覆盖膜材料的厚度为1μm~80μm,优选为5μm~60μm,更优选为10μm~30μm。
在一些具体的实施例中,载体膜材料优选透光率≥95%的塑料薄膜,如聚酯薄膜(PET)、聚丙烯薄膜(PP)、聚酰亚胺薄膜(PI)、聚乙烯薄膜(PE)、聚氯乙烯薄膜(PVC)、聚醚醚酮薄膜(PEEK)、聚碳酸酯薄膜(PC)、乙烯薄膜(PS)等中的一种。当载体膜的透光率低于95%时,使用胶膜材料制造器件过程中影响激光钻孔精度,导致所钻孔真圆度和垂直度低。
本发明另一个方面提供了一种上述绝缘胶膜材料的制备方法,其包括以下步骤:
S1)将制备介质膜电子浆料的原料进行混合,获得介质膜的电子浆料;
S2)将介质膜的电子浆料涂覆在载体膜表面,并干燥获得负载介质膜的载体膜;
S3)将覆盖膜覆盖在介质膜表面进行贴合,得到绝缘胶膜材料。
在一些具体的实施例中,所述介质膜电子浆料的原料包括环氧树脂、填料、固化剂和溶剂。
在一些具体的实施例中,所述介质膜电子浆料的原料还包括改性剂,所述改性剂选自二异氰酸酯化合物,所述二异氰酸酯化合物选自氢化二苯甲烷二异氰酸酯、异氟尔酮二异氰酸酯、甲苯二异氰酸酯、二苯基甲烷二异氰酸酯、二环己基甲烷二异氰酸酯、六亚甲基二异氰酸酯、赖氨酸二异氰酸酯。
进一步地,电子浆料的混合方法包括搅拌、球磨、砂磨、超声等中的一种或多种组合使用。
进一步地,电子浆料的涂覆方式选自凹版印刷、微凹版印刷、逗号刮刀、狭缝挤出。
进一步地,干燥的温度为50℃~150℃。
进一步地,贴合温度为室温至150℃,贴合的方法为热压贴合。
本发明又一个方面提供了上述任一绝缘胶膜材料作为半导体电子封装材料中的电介质层中的用途,所述半导体电子封装材料为封装基板、封装载板、扇出型板级封装再布线的材料。
实施例1
采用连续法制备本发明所涉及的多层绝缘胶膜材料的方法,使用配方A中介质膜电子浆料。
选用热膨胀系数为20ppm/K,Tg为95℃,离型剂厚度为1.2μm的PET离型膜作为载体膜进行刮涂,介质膜的厚度为20μm。玻璃化转变温度Tg由TMA拉伸测试方法测得。然后进行70℃,3分钟烘干。干燥后的绝缘聚合物复合物薄膜与厚度20μm的BOPP薄膜进行热压复合,热压过程中,加热辊的温度设置为80℃,加热压力为5kg。经过热压后得到具有三层结构的绝缘胶膜材料,然后将BOPP膜进行剥离,最后进行100℃,30分钟,180℃,90分钟固化。经过上述方法测试后,绝缘胶膜材料烘干以及固化后,未出现卷曲以及离型膜与介质层出现分层的现象。
实施例2
使用配方B作为介质膜的电子浆料涂在热膨胀系数为15ppm/K,Tg为85℃,离型剂厚度为1.5μm的PET离型膜作为载体膜进行刮涂,介质膜的厚度为25μm,然后进行50℃,2分钟,70℃,3分钟烘干。干燥后的绝缘聚合物复合物薄膜与厚度15μm的BOPP薄膜进行热压复合,热压过程中,加热辊的温度设置为80℃,加热压力为5kg。经过热压后得到具有三 层结构的绝缘胶膜材料,然后将BOPP进行剥离。最后进行100℃,30分钟,180℃,90分钟固化。经过上述方法测试后,绝缘胶膜材料烘干以及固化后,未出现卷曲以及离型膜与介质层出现分层的现象。
实施例3
使用配方C作为介质膜中的电子浆料,涂在热膨胀系数为8ppm/K,Tg为83℃,离型剂厚度为1.8μm的PET离型膜作为载体膜进行刮涂,介质膜的厚度为23μm,然后进行60℃,5分钟烘干。干燥后的绝缘聚合物复合物薄膜与厚度26μm的BOPP薄膜进行热压复合,热压过程中,加热辊的温度设置为80℃,加热压力为5kg。经过热压后得到具有三层结构的绝缘胶膜材料。最后进行100℃,30分钟,180℃,90分钟固化。经过上述方法测试后,绝缘胶膜材料烘干以及固化后,未出现卷曲以及离型膜与介质层出现分层的现象。
对比例1
采使用配方A作为介质膜中的电子浆料,涂在热膨胀系数为50ppm/K,Tg为65℃,离型剂厚度为2μm的PET离型膜作为载体膜进行刮涂,介质膜的厚度为23μm,然后进行60℃,5分钟烘干。干燥后取出,发现载体膜与介质出现弯曲现象,无法进行下一步与BOPP的压合,严重影响元器件的可靠性。
对比例2
使用配方B作为介质膜中的电子浆料,涂在热膨胀系数为80ppm/K,Tg为50℃,离型剂厚度为1.2μm的PET离型膜作为载体膜进行刮涂,介质膜的厚度为25μm,然后进行60℃,5分钟烘干。干燥后取出,发现载体膜与介质出现弯曲现象,无法进行下一步与BOPP的压合,严重影响元器件的可靠性。
对比例3
使用配方C作为介质膜中的电子浆料,涂在热膨胀系数为36ppm/K,Tg为75℃,离型剂厚度为1.5μm的PET离型膜作为载体膜进行刮涂,介质膜的厚度为25μm,然后进行60℃,5分钟烘干。干燥后取出,将绝缘聚合物复合物薄膜与厚度20μm的BOPP薄膜进行热压复合,热压过程中,加热辊的温度设置为80℃,加热压力为5kg。经过热压后得到具有三层结构的绝缘胶膜材料。最后进行100℃,30分钟,180℃,90分钟固化。将固化后的绝缘胶膜材料取出后发现载体膜与介质层出现分离的现象,导致绝缘胶膜材料的可靠性降低,从而影响元器件的性能与可靠性。
Claims (10)
- 一种绝缘胶膜材料,绝缘胶膜材料由载体膜、介质膜和覆盖膜组成,其中介质膜位于载体膜和覆盖膜中间形成三明治结构;其特征在于,所述载体膜的玻璃化转变温度为80℃以上;且所述载体膜在30~80℃温度区间的热膨胀系数为30ppm/K以下;且所述载体膜表面涂覆有离型剂;优选地,所述载体膜的玻璃化转变温度80℃-120℃。优选为,载体膜在30~80℃温度区间的热膨胀系数25ppm/K以下,优选为15ppm/K以下,更优选为5ppm/K以下。
- 权利要求1所述的绝缘胶膜材料,其特征在于,所述离型剂的厚度为0.3~5μm,优选为0.5~4μm,更优选为1~3μm。
- 权利要求1所述的绝缘胶膜材料,其特征在于,载体膜材料选自透光率95%以上的塑料薄膜,优选为聚酯薄膜(PET)、聚丙烯薄膜(PP)、聚酰亚胺薄膜(PI)、聚乙烯薄膜(PE)、聚氯乙烯薄膜(PVC)、聚醚醚酮薄膜(PEEK)、聚碳酸酯薄膜(PC)、乙烯薄膜(PS)中的一种。
- 权利要求1所述的绝缘胶膜材料,其特征在于,所述介质膜由电子浆料制成,所述电子浆料中包含环氧树脂、固化剂、填料和溶剂;优选地,所述电子浆料中还包含改性剂,所述改性剂选自二异氰酸酯化合物,所述二异氰酸酯化合物选自氢化二苯甲烷二异氰酸酯、异氟尔酮二异氰酸酯、甲苯二异氰酸酯、二苯基甲烷二异氰酸酯、二环己基甲烷二异氰酸酯、六亚甲基二异氰酸酯、赖氨酸二异氰酸酯。
- 权利要求1所述的绝缘胶膜材料,其特征在于,介质膜的厚度为0.5~200μm,优选为20~80μm,更优选为30~50μm。
- 权利要求3所述的绝缘胶膜材料,其特征在于,所述环氧树脂选自双酚A型环氧树脂、双酚F型环氧树脂、酚醛型环氧树脂、邻甲酚醛型环氧树脂、多官能团环氧树脂、脂环族环氧树脂、间苯二酚环氧树脂、橡胶改性环氧树脂、聚氨酯改性环氧树脂、联苯环氧树脂、双环戊二烯环氧树脂、溴化环氧树脂;所述固化剂为分子结构中含有能够与环氧基发生反应的氨基、羟基、酚羟基、羧基、酸酐、氰基、酯基中的一种或多种的化合物;所述溶剂为可挥发溶剂。
- 权利要求1所述的绝缘胶膜材料,其特征在于,覆盖膜材料选自聚合物薄膜材料、纸基膜材料;优选地,所述聚合物薄膜材料选自双向拉伸聚丙烯薄膜(BOPP)、聚酯薄膜(PET)、聚醚醚酮薄膜(PEEK)、聚醚酰亚胺薄膜(PEI)、聚酰亚胺薄膜(PI)、聚碳酸酯薄膜(PC);纸基膜材料选自离型纸、淋膜纸。
- 权利要求1所述的绝缘胶膜材料,其特征在于,覆盖膜材料的厚度为1μm~80μm。
- 权利要求1-8任一项所述的绝缘胶膜材料的制备方法,其包括以下步骤:S1)将制备介质膜电子浆料的原料进行混合,获得介质膜的电子浆料;S2)将介质膜的电子浆料涂覆在载体膜表面,并干燥获得负载介质膜的载体膜;S3)将覆盖膜覆盖在介质膜表面进行贴合,得到绝缘胶膜材料;所述介质膜电子浆料的原料包括环氧树脂、填料、固化剂和溶剂;优选地,所述介质膜电子浆料的原料还包括改性剂,所述改性剂选自二异氰酸酯化合物;优选地,电子浆料的混合方法包括搅拌、球磨、砂磨、超声等中的一种或多种组合使用;优选地,电子浆料的涂覆方式选自凹版印刷、微凹版印刷、逗号刮刀、狭缝挤出;优选地,干燥的温度为50℃~150℃;优选地,贴合温度为室温至150℃,贴合的方法为热压贴合。
- 权利要求1-8任一项所述的绝缘胶膜材料作为半导体电子封装材料中的电介质层中的用途,所述半导体电子封装材料为封装基板、封装载板、扇出型板级封装再布线的材料。
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