EP2638570A1 - Klebmasse und verfahren zur kapselung einer elektronischen anordnung - Google Patents

Klebmasse und verfahren zur kapselung einer elektronischen anordnung

Info

Publication number
EP2638570A1
EP2638570A1 EP11779147.5A EP11779147A EP2638570A1 EP 2638570 A1 EP2638570 A1 EP 2638570A1 EP 11779147 A EP11779147 A EP 11779147A EP 2638570 A1 EP2638570 A1 EP 2638570A1
Authority
EP
European Patent Office
Prior art keywords
adhesive
electronic
pressure
psa
opto
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP11779147.5A
Other languages
German (de)
English (en)
French (fr)
Inventor
Alexander Steen
Thorsten Krawinkel
Klaus KEITE-TELGENBÜSCHER
Judith Grünauer
Jan Ellinger
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tesa SE
Original Assignee
Tesa SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tesa SE filed Critical Tesa SE
Publication of EP2638570A1 publication Critical patent/EP2638570A1/de
Withdrawn legal-status Critical Current

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Classifications

    • 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
    • C09J109/00—Adhesives based on homopolymers or copolymers of conjugated diene hydrocarbons
    • C09J109/06—Copolymers with styrene
    • 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
    • C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
    • 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
    • C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
    • C09J153/005—Modified block copolymers
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00—Details of semiconductor or other solid state devices
    • H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00—Details of semiconductor or other solid state devices
    • H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
    • H01L23/29—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
    • H01L23/293—Organic, e.g. plastic
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001—Technical content checked by a classifier
    • H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/10—Details of semiconductor or other solid state devices to be connected
    • H01L2924/11—Device type
    • H01L2924/12—Passive devices, e.g. 2 terminal devices
    • H01L2924/1204—Optical Diode
    • H01L2924/12044—OLED

Definitions

  • Adhesive composition and method for encapsulating an electronic device The present invention relates to an adhesive composition for the encapsulation of an electronic device and to a method for its use.
  • (Opto) electronic arrangements are increasingly used in commercial products or are about to be launched. Such arrangements include inorganic or organic electronic structures, such as organic, organometallic or polymeric semiconductors or combinations thereof. These arrangements and products are rigid or flexible depending on the desired application, whereby there is an increasing demand for flexible arrangements.
  • Electrophoretic or electrochromic structures or displays, organic or polymeric light-emitting diodes (OLEDs or PLEDs) in display and display devices or as illumination, electroluminescent lamps, light-emitting electrochemical devices may be mentioned as examples of (commercial) electronic applications which are already interesting in their market potential Cells (LEECs), organic solar cells, preferably dye or polymer solar cells, inorganic solar cells, preferably thin-film solar cells, in particular based on silicon, germanium, copper, indium and selenium, organic field-effect transistors, organic Switching elements, organic optical amplifiers, organic laser diodes, organic or inorganic sensors or organic or inorganic-based RFID transponder listed.
  • LECs Light-emitting electrochemical devices
  • Permeants can be a variety of low molecular weight organic or inorganic compounds, especially water vapor and oxygen.
  • inorganic and / or organic (opto) electronics in particular in organic (opto) electronics, there is a particular need for flexible adhesive solutions which represent a permeation barrier for permeants such as oxygen and / or water vapor.
  • the flexible adhesive solutions should therefore not only achieve good adhesion between two substrates, but additionally meet properties such as high shear strength and peel strength, chemical resistance, aging resistance, high transparency, easy processability and high flexibility and flexibility.
  • a common approach in the art is therefore to allow the electronic assembly between two water vapor and oxygen impermeable substrates lay. This is followed by a seal at the edges.
  • glass or metal substrates are used which offer a high permeation barrier but are very susceptible to mechanical stress. Furthermore, these substrates cause a relatively large thickness of the entire assembly. In the case of metal substrates, there is also no transparency.
  • surface substrates such as transparent or non-transparent films are used, which can be designed in multiple layers. Here, both combinations of different polymers, as well as inorganic or organic layers can be used. The use of such surface substrates allows a flexible, extremely thin structure.
  • substrates such as films, fabrics, nonwovens and papers or combinations thereof are possible for the various applications.
  • a good adhesive for the sealing of (opto) electronic components has a low permeability to oxygen and in particular to water vapor, has sufficient adhesion to the assembly and can flow well on this. Low adhesion to the assembly reduces the barrier effect at the interface, allowing oxygen and water vapor to enter regardless of the properties of the adhesive. Only if the contact between mass and substrate is continuous, the mass properties are the determining factor for the barrier effect of the adhesive.
  • the oxygen transmission rate OTR Olygen Transmission Rate
  • the water vapor transmission rate WVTR Water Vapor Transmission Rate
  • the respective rate indicates the area- and time-related flow of oxygen or water vapor through a film under specific conditions of temperature and partial pressure and optionally other measurement conditions such as relative humidity. The lower these values are, the better the respective material is suitable for encapsulation.
  • the specification of the permeation is based not only on the values for WVTR or OTR but always includes an indication of the mean path length of the permeation, such as the thickness of the material, or a normalization to a certain path length.
  • the permeability P is a measure of the permeability of a body to gases and / or liquids.
  • the permeability P is a specific value for a defined material and a defined permeant under steady state conditions at a given permeation path length, partial pressure and temperature.
  • the permeability P is the product of diffusion term D and solubility term S:
  • the solubility term S describes predominantly the affinity of the barrier adhesive to the permeant. For example, in the case of water vapor, a small value for S of hydrophobic materials is achieved.
  • the diffusion term D is a measure of the mobility of the permeant in the barrier material and is directly dependent on properties such as molecular mobility or free volume. Often relatively low values are achieved for strongly cross-linked or highly crystalline D materials. However, highly crystalline materials tend to be less transparent and greater crosslinking results in less flexibility.
  • the permeability P usually increases with an increase in molecular mobility, such as when the temperature is increased or the glass transition point is exceeded.
  • liquid adhesives and adhesives based on epoxides have been used (WO 98/21287 A1, US 4,051,195 A, US 4,552,604 A). These have a low diffusion term D due to strong cross-linking. Their main application is edge bonding of rigid arrangements, but also moderately flexible arrangements. Curing takes place thermally or by means of UV radiation. A full-surface bonding is hardly possible due to the shrinkage caused by the curing, since it comes to tensions between adhesive and substrate during curing, which in turn can lead to delamination.
  • liquid adhesives have a number of disadvantages.
  • VOCs low-molecular-weight components
  • the adhesive must be applied consuming each individual component of the arrangement.
  • the purchase of expensive dispensers and fixators is necessary to ensure accurate positioning.
  • the type of application also prevents a rapid continuous process and also by the subsequently required lamination step, the achievement of a defined layer thickness and bond width can be made difficult within narrow limits by the low viscosity.
  • thermal-crosslinking systems are limited in the low temperature range or in 2-component systems by the pot life, ie the processing time until a gelling has taken place.
  • the sensitive (opto) electronic structures limit the usability of such systems - the maximum applicable temperatures in (opto) electronic structures are sometimes only at 60 ° C, since a pre-damage already occurs from this temperature can.
  • flexible arrangements which contain organic electronics and are encapsulated with transparent polymer films or composites of polymer films and inorganic layers have narrow limits here. This also applies to laminating under high pressure. To achieve improved durability is here a waiver of a temperature-stressing step and a lamination under a lower pressure of advantage.
  • US 2006/0100299 A1 discloses a UV-curable pressure-sensitive adhesive tape for encapsulating an electronic device.
  • the pressure-sensitive adhesive tape comprises an adhesive based on a combination of a polymer having a softening point greater than 60 ° C., a polymerizable epoxy resin having a softening point of below 30 ° C. and a photoinitiator.
  • the polymers may be polyurethane, polyisobutylene, polyacrylonitrile, polyvinylidene chloride, poly (meth) acrylate or polyester, but especially an acrylate.
  • adhesive resins, plasticizers or fillers are included.
  • Acrylic compounds have a very good resistance to UV radiation and various chemicals, but have very different bond strengths on different substrates. While the bond strength on polar substrates such as glass or metal is very high, the bond strength on nonpolar substrates such as polyethylene or polypropylene is rather low. Here there is a danger of diffusion at the Interface in particular. In addition, these masses are very polar, which favors a diffusion of water vapor in particular, despite subsequent networking. The use of polymerisable epoxy resins further strengthens this tendency. Pressure-sensitive adhesive tapes generally require a certain amount of time, sufficient pressure and a good balance between the viscous component and the elastic component as a result of the relatively high molecular weight polymers, in contrast to liquid adhesives, for good wetting and adhesion to the surface.
  • WO 2007/087281 A1 discloses a transparent flexible pressure-sensitive adhesive tape based on polyisobutylene (PIB) for electronic applications, in particular OLED.
  • PIB polyisobutylene
  • polyisobutylene having a molecular weight of more than 500,000 g / mol and a hydrogenated cyclic resin is used.
  • the use of a photopolymerizable resin and a photoinitiator is possible.
  • Adhesives based on polyisobutylene have a good barrier to water vapor due to their low polarity, but have a relatively low cohesiveness even at high molecular weights, which is why they often have a low shear strength at elevated temperatures.
  • the proportion of low molecular weight components can not be reduced arbitrarily, otherwise the adhesion is significantly reduced and the interfacial permeation increases.
  • the polarity of the mass is increased again and thus increases the solubility term.
  • the formation of at least two domains within the block copolymer additionally gives a very good cohesion at room temperature and at the same time improved barrier properties.
  • a PSA is also known from the prior art (WO 03/065470 A1), which is used in an electronic structure as a transfer adhesive.
  • the adhesive contains an inorganic functional filler that reacts with oxygen or water vapor within the assembly. For a simple application of a getter within the structure is possible.
  • another low permeability adhesive is used.
  • the object of the present invention is to provide an adhesive for the encapsulation of an electronic device against permeants, especially water vapor, which is transparent, which provides a good barrier to water vapor, the elastomer can react with water, whereby the breakthrough time of water in particular is increased , which increases the breakthrough time, in particular of water, and with the same time a good encapsulation can be achieved.
  • the invention relates to the use of an adhesive comprising an organometallic modified polymer formed by reaction of an elastomer with an organometallic compound, wherein the central atom of the organometallic compound is a metal or semimetal of the 3rd and 4th main group or the 3rd and 4th subgroup.
  • the modified polymer is capable of reacting with moisture.
  • the organometallic compound can be introduced both by a reaction via a functional group in the polymer, as well as by a radical reaction with a double bond present in the polymer chain.
  • a reactive group may be, for example, an epoxy or anhydride group, but also an amino group is conceivable.
  • This group can then react with a corresponding group in the organometallic compounds to form a polymer with organometallic modification.
  • an epoxy or anhydride group for example, this can react with an amino group in the organometallic compound.
  • M Si, Sn, Pb, Ti, Zr
  • R 1 , R 2 are independently selected from the group methyl, ethyl,
  • n 1 to 12
  • Y a functional group selected from the group
  • Silanes and titanates with an amino or sulfide group are particularly preferred.
  • the reaction with the polymers can be done spontaneously in solution or can be accelerated by heating and adding catalysts such as acids. Ideally, the reaction is spontaneous, so that all components of the adhesive, in addition to the polymers and organometallic compounds, the tackifiers, plasticizers and other auxiliaries, can be brought into solution simultaneously, and the reaction takes place during the dissolution of the individual components.
  • An attachment of an organometallic compound of the present invention can also be introduced via double bonds in the polymer, if the organometallic compound also contains at least one double bond.
  • organometallic compounds are sensitive to water, anhydrous solvents should be used.
  • organometallic compounds with vinyl, acrylic or methacrylic groups can be used.
  • organometallic compounds of the following form may be included:
  • M Si, Sn, Pb, Ti, Zr
  • R 1 , R 2 independently selected from the group methyl, ethyl,
  • R 3 H or CH 3
  • n 1 to 12
  • polymers in which a silane group has been introduced via this route have been known for some time, for example from EP 0 827 994 A1, but application as barrier adhesives has not been described. If the polymers contain double bonds to which the organometallic compounds are to be linked via a free-radical reaction, it is advantageous if the number of double bonds is not too high, so that crosslinking of the polymers does not take place during the free-radical reaction. It is therefore preferred to use partially hydrogenated polymers. The same applies if the double bonds of the polymers are converted into epoxides only by a reaction with, for example, peracids.
  • Polymers with double bonds for modification can be, for example, polymers with butadiene or isoprene monomers, such as polybutadiene, polyisoprene, styrene-butadiene rubbers, block copolymers of vinylaromatics and isoprene or butadiene, as described in more detail below, block copolymers of isoprene and butadiene, nitrile rubber, ABS or similar.
  • Polymers of ethylene-propylene with another monomer having two double bonds for example EPDM, can also be used.
  • Polymers having reactive groups to which organometallic compounds can be attached are, for example, systems containing epoxide or anhydride groups. As polymers are used, for example, the following.
  • Epoxidizable polymers having a double bond may be those described above.
  • Acid anhydride-containing polymers according to the invention can be used both those which have been prepared by modification of finished polymers with, for example, maleic anhydride under free-radical conditions, as well as those which have incorporated anhydride-containing monomers in the main or side chain.
  • modified polymers a number of polyolefins, such as polyethylene or polypropylene, but also poly- ⁇ -olefins, polymerized from ethylene and at least one other ⁇ -olefin, polybutenes, as well as block copolymers of ethylene and propylene can be used.
  • block copolymers of a vinyl aromatic and a diene are useful, especially when the majority of the remaining double bonds is hydrogenated. In all these polymers, the content of double bonds is preferably very low, since it is in the reaction of the polymers with Otherwise, the acid anhydrides can easily lead to undesirable crosslinking reactions.
  • block copolymers comprising polymer blocks predominantly formed of vinylaromatics (A blocks), preferably styrene, and those predominantly formed by polymerization of 1,3-dienes (B blocks), preferably butadiene, isoprene or a mixture of both monomers. These B blocks usually have a low polarity. Both homo- and copolymer blocks are preferably usable as B blocks. Block copolymers with polyisobutylene in the main chain can also be used.
  • the block copolymers resulting from the A and B blocks may contain the same or different B blocks, which may be partially, selectively or preferably fully hydrogenated.
  • the block copolymers may have linear A-B-A structures. It is also possible to use block copolymers of radial form as well as star-shaped and linear multiblock copolymers. As further components, A-B diblock copolymers may be present. All of the aforementioned polymers can be used alone or in admixture with each other. It is also possible to use block copolymers which, in addition to the above-described blocks A and B, contain at least one further block, for example A-B-C block copolymers.
  • the block copolymers have a Polyvinylaromatenanteil of 10 wt .-% to 35 wt .-%.
  • the proportion of vinylaromatic block copolymers in total, based on the total pressure-sensitive adhesive mass is preferably at least 30% by weight, preferably at least 40% by weight, more preferably at least 45% by weight. Too low a proportion of vinylaromatic block copolymers has the consequence that the cohesion of the PSA is relatively low.
  • the maximum proportion of the vinylaromatic block copolymers in total, based on the total PSA is at most 80% by weight, preferably at most 70% by weight. Too high a proportion of vinylaromatic block copolymers, in turn, has the consequence that the PSA is barely tacky.
  • At least part of the block copolymers used is acid-anhydride-modified or epoxidized or still has double bonds.
  • the anhydride modification is carried out mainly by free-radical graft copolymerization of unsaturated acid anhydrides, such as maleic anhydride, citraconic anhydride, dimethylmaleic anhydride, ethyl and diethylmaleic anhydride, chloro and dichloromaleic anhydride,
  • unsaturated acid anhydrides such as maleic anhydride, citraconic anhydride, dimethylmaleic anhydride, ethyl and diethylmaleic anhydride, chloro and dichloromaleic anhydride
  • Tetrahydrophthalic anhydride or methyltetrahydrophthalic anhydride preferably maleic anhydride.
  • the proportion of acid or acid anhydride is preferably between 0.5 and 4 percent by weight based on the total block copolymer.
  • the epoxide modification takes place by reaction with peracids of block copolymers still containing double bonds.
  • epoxidizing agents are hydrogen peroxide with different catalysts, tert-butyl hydroperoxide, meta-chloroperbenzoic acid (MCPBA), or peroxy-ante- or peroxyacetic acid, which are prepared in situ.
  • Polymers in which the acid anhydride is incorporated directly into the polymer chain are, for example, polymers of styrene and maleic anhydride, mostly alternating, such as SMA polymers from Sartomer, polymers of ethylene and maleic anhydride, such as Gantrez polymers of the company ISP or isobutylene and maleic anhydride, such as Isobam Kuraray, just to name a few
  • the adhesive is a pressure-sensitive adhesive, so a viscoelastic composition which remains permanently tacky and tacky at room temperature in a dry state. The bonding takes place by light pressure immediately on almost all substrates.
  • the adhesive may also be a hotmelt adhesive, ie a water-free and solvent-free adhesive which is solid at room temperature and which is applied to the parts to be bonded from the melt and physically sets after consolidation on cooling to solidify.
  • a hotmelt adhesive ie a water-free and solvent-free adhesive which is solid at room temperature and which is applied to the parts to be bonded from the melt and physically sets after consolidation on cooling to solidify.
  • tackifiers are preferably used.
  • Adhesive resins which are compatible with the silane-modified polymer and with the soft blocks in the vinylaromatic block copolymers serve this purpose.
  • Suitable tackifier resins include, but are not limited to, non-hydrogenated, partially or fully hydrogenated rosin and rosin derivative resins, hydrogenated polymers of dicyclopentadiene, non-hydrogenated, partially, selectively or fully hydrogenated hydrocarbon resins based on C 5 , C 5 / C 9 . or C 9 - Monomerströmen, polyterpene resins based on ⁇ -pinene and / or ⁇ -pinene and / or ⁇ -limonene, hydrogenated polymers of preferably pure C 8 - and C 9 aromatics.
  • the aforementioned adhesive resins can be used both alone and in admixture. Both solid and liquid resins can be used at room temperature.
  • hydrogenated resins having a degree of hydrogenation of at least 90%, preferably of at least 95%, are preferred.
  • non-polar resins with a DACP value (diacetone alcohol cloud point) above 30 ° C. and a MMAP value (mixed methylcyclohexane aniline point) of greater than 50 ° C., in particular with a DACP value above 37 ° C. and a MMAP value greater than 60 ° C preferred.
  • the DACP value and the MMAP value each indicate the solubility in a particular solvent.
  • Resins having a softening point (ring / ball, determination according to DIN EN ISO 4625) of more than 95 ° C., in particular more than 100 ° C., are also preferred. Through this Selection a particularly high permeation barrier, especially against oxygen, achieved.
  • the softening point is the temperature (or the temperature range) at which glasses, amorphous or partially crystalline polymers change from the glassy, hard-elastic to a soft state.
  • the reduction in the hardness of corresponding substances at the softening point is made clear, for example, by the fact that a body applied to a substance sample under load is pressed into it when the softening point is reached.
  • the softening point is always above the glass transition temperature, but in most polymers, well below the temperature at which they are completely in the liquid state.
  • the adhesive contains tackifiers, preferably to a proportion of up to 60 wt .-% based on the total amount. In the case of a hot melt adhesive, the proportion may be lower, for example up to 30 wt .-% based on the total amount.
  • additives can typically be used:
  • Plasticizers such as plasticizer oils or low molecular weight liquid polymers such as low molecular weight polybutenes
  • Sunscreens such as UV absorbers or hindered amines
  • further polymers of preferably elastomeric nature include, but are not limited to, those based on pure hydrocarbons, for example, unsaturated polydienes such as natural or synthetically produced polyisoprene or polybutadiene, chemically substantially saturated elastomers such as saturated ethylene-propylene copolymers, ⁇ -olefin copolymers, polyisobutylene, butyl rubber, ethylene-propylene rubber, and chemically functionalized hydrocarbons such as halogen-containing, acrylate-containing, allyl or vinyl ether-containing polyolefins.
  • unsaturated polydienes such as natural or synthetically produced polyisoprene or polybutadiene
  • chemically substantially saturated elastomers such as saturated ethylene-propylene copolymers, ⁇ -olefin copolymers, polyisobutylene, butyl rubber, ethylene-propylene rubber
  • chemically functionalized hydrocarbons such as halogen-containing, acrylate
  • the adhesive according to the invention is also suitable without the resins and / or additives listed depending on the application, be it that the resins and / or additives are omitted in their entirety, in any combination or individually.
  • the adhesive according to the invention omits inorganic silicates and aluminosilicates.
  • the present invention is based initially on the finding that, despite the disadvantages described above, it is nevertheless possible to use a melt or pressure-sensitive adhesive for encapsulating an electronic arrangement in which the disadvantages described above with regard to PSAs do not occur or only diminish. It has been found that enamel or PSAs which contain a getter covalently bound to the polymer are particularly well suited for the encapsulation of electronic components since, on the one hand, there is no risk of an organic (fluid) getter entering the electronic system migrated active components and leads there to damage and on the other hand, the occurring during the use of particulate getter adhesive reduction and resulting turbidity of the adhesive is avoided.
  • PSAs are characterized in particular by their permanent tackiness and flexibility.
  • a material that exhibits permanent tack must have a suitable combination of adhesive and cohesive properties at all times. This characteristic distinguishes the pressure-sensitive adhesives, for example, from reactive adhesives which hardly provide cohesion in the unreacted state. For good adhesion properties, To adjust pressure-sensitive adhesives so that an optimal balance of adhesive and cohesive properties exists.
  • encapsulation is not only a complete enclosure with said PSA, but also a partial application of the PSA to the areas of the (opto) electronic device to be encapsulated, for example a one-sided overlap or a framing of an electronic structure.
  • a low permeability of permeants such as water vapor and oxygen is achieved, but in particular of water vapor.
  • the incorporated silane continues to increase the breakthrough time.
  • the advantage of the present invention is thus compared to other PSAs, the combination of very good barrier properties to oxygen and especially to water vapor with good interfacial adhesion to different substrates, good cohesive properties, compared to liquid adhesives, a very high flexibility and a simple application in the (opto) electronic arrangement and with / in the encapsulation. Furthermore, in certain embodiments, there are also transparent adhesives that can be used in a special way for use in (opto) electronic arrangements, since a reduction of incident or emerging light is kept very low.
  • Such a PSA can be easily integrated into an electronic device, especially in such an arrangement that requires high flexibility. Further particularly advantageous properties of the pressure-sensitive adhesive are similarly good adhesion to different substrates, high shear strength and high flexibility. By a very good adhesion to the substrate also a small Grenz moralpermeation is achieved.
  • the mass can be easily and quickly integrated under low pressure in the encapsulation process of the (opto) - electronic structure.
  • the disadvantages usually associated with the avoided processing steps, such as thermal and mechanical stresses, can thus be minimized.
  • Encapsulation by lamination of at least parts of the (opto) electronic structures with a flat barrier material is possible with very good barrier effect in a simple roll-to-roll process .
  • a flat barrier material for example glass, especially thin glass, metal oxide coated films, metal foils, multilayer substrate materials
  • the flexibility of the entire structure depends, in addition to the flexibility of the PSA, on other factors such as geometry and thickness of the (opto) electronic structures or the surface barrier materials.
  • the high flexibility of the PSA makes it possible to realize very thin, flexible and flexible (opto) electronic structures.
  • flexible is meant the property of following the curvature of a curved article such as a drum of certain radius, in particular a radius of 1 mm, without damage.
  • the PSA according to the invention is heated during or after the application.
  • the temperature should preferably be more than 30 ° C., more preferably more than 50 ° C., in order to promote the flow accordingly.
  • the temperature should not be selected too high in order not to damage the (opto) electronic arrangement.
  • the PSA may be provided in the form of an adhesive tape. This mode of administration allows a particularly simple and uniform application of the PSA.
  • the general term "adhesive tape” encompasses a carrier material which is provided on one or both sides with a pressure-sensitive adhesive
  • the carrier material comprises all planar structures, for example films or film sections expanded in two dimensions, belts of extended length and limited width, belt sections , Diecuts, multi-layer arrangements and the like.
  • the tape can be provided in fixed lengths such as by the meter or as an endless product on rolls (Archimedean spiral).
  • support it is possible to use all known supports, for example scrims, woven fabrics, knitted fabrics, nonwovens, films, papers, tissues, foams and foamed films.
  • preference is given to using polymer films, film composites or films or film composites provided with organic and / or inorganic layers.
  • films / film composites can consist of all common plastics used for film production, but are not to be mentioned as examples by way of non-limiting example:
  • Polyethylene polypropylene - especially the oriented polypropylene (OPP) produced by mono- or biaxial stretching, cyclic olefin copolymers (COC), polyvinyl chloride (PVC), polyesters - in particular polyethylene terephthalate (PET) and polyethylene naphthalate (PEN), ethylene vinyl alcohol (EVOH), polyvinylidene chloride (PVDC), polyvinylidene fluoride (PVDF), polyacrylonitrile (PAN), polycarbonate (PC), polyamide (PA), polyethersulfone (PES) or polyimide (PI).
  • OPP oriented polypropylene
  • COC cyclic olefin copolymers
  • PVC polyvinyl chloride
  • PET polyethylene terephthalate
  • PEN polyethylene naphthalate
  • EVOH ethylene vinyl alcohol
  • PVDC polyvinylidene chloride
  • PVDF polyvinylidene fluoride
  • PAN polyacrylonit
  • crosslinked polyethylene foams or viscoelastic supports are suitable.
  • the latter are preferably made of polyacrylate, more preferably filled with hollow bodies of glass or polymers.
  • the backings may be prepared by priming or physical pretreatment such as corona or etching prior to contacting with the adhesive.
  • the carrier may also be multi-layered, for example by laminating different layers together or coextruding layers.
  • the support may also be combined with organic or inorganic coatings or layers. This can be done by conventional methods such as painting, printing, evaporation, sputtering, co-extrusion or lamination.
  • oxides or nitrides of silicon and aluminum indium-tin oxide (ITO) or sol-gel coatings.
  • These films / film composites, in particular the polymer films, are particularly preferably provided with a permeation barrier for oxygen and water vapor, the permeation barrier exceeding the requirements for the packaging area (WVTR ⁇ 10 "1 g / (m 2 d); OTR ⁇ 10 " 1 cm 3 / (m 2 d bar)).
  • the determination of the permeability to oxygen (OTR) and water vapor (WVTR) is carried out according to DIN 53380 Part 3 or ASTM F-1249.
  • the oxygen permeability is measured at 23 ° C and a relative humidity of 50%.
  • the water vapor permeability is determined at 37.5 ° C and a relative humidity of 90%.
  • the results are normalized to a film thickness of 50 ⁇ .
  • the films / film composites may be made transparent, so that the overall structure of such an adhesive article is transparent.
  • Transparency means an average transmission in the visible range of light of at least 75%, preferably higher than 90%.
  • adheresive tape also includes so-called “transfer tapes”, that is, an adhesive tape without a carrier.
  • transfer adhesive tape the adhesive is applied before application between flexible liners which are provided with a release layer and / or have anti-adhesive properties.
  • a liner is first removed, the adhesive is applied and then the second liner is removed.
  • the PSA can thus be used directly for the connection of two surfaces in (opto) electronic arrangements.
  • a pressure-sensitive adhesive is used, which is transparent in certain embodiments in the visible light of the spectrum (wavelength range of about 400 nm to 800 nm). For certain applications, such as solar cells, this range can also be extended to defined UV or IR regions. The desired transparency in the preferred range of the visible spectrum can be achieved in particular by the use of colorless adhesive resins.
  • Such a pressure-sensitive adhesive is thus also suitable for full-surface use over an (opto) electronic structure.
  • a full-surface bonding offers, with an approximately central arrangement of the electronic structure in relation to an edge seal, the advantage that the permeant would have to diffuse through the entire surface before it reaches the structure. The permeation path is thus significantly increased.
  • the permeation paths extended in this embodiment compared to edge sealing, such as liquid adhesives have a positive effect on the overall barrier, since the permeation path is inversely proportional to the permeability.
  • transparency means an average transmission of the adhesive in the visible range of light of at least 75%, preferably higher than 90%
  • maximum transmission of the entire assembly also depends on the type of carrier used and on the carrier Type of construction.
  • UV-blocking denotes an average transmittance of not more than 20%, preferably not more than 10%, more preferably not more than 1% in the corresponding wavelength range.
  • UVA radiation formed UV blocking, preferably in the wavelength range of 280 nm to 400 nm (UVA and UVB radiation), more preferably in the wavelength range of 190 nm to 400 nm (UVA, UVB and UVC radiation).
  • the UV-blocking effect of the PSA can be achieved in particular by adding UV blockers or suitable fillers to the PSA.
  • Suitable UV blockers are, for example, HALS (Hinder Armine Light Stabilizer) such as Tinuvin from BASF or benzimidazole derivatives.
  • HALS Hader Armine Light Stabilizer
  • the filler is titanium dioxide, in particular nanoscale titanium dioxide, since this allows transparency to be maintained in the visible range.
  • the PSA shows a very good resistance to weathering and UV light. This resistance can be achieved in particular by using hydrogenated elastomers and / or hydrogenated resins.
  • the preparation and processing of the PSA can be carried out from solution, dispersion and from the melt.
  • the preparation and processing takes place from solution or from the melt.
  • Particularly preferred is the production of the adhesive from solution.
  • the components of the PSA are dissolved in a suitable solvent, for example toluene or mixtures of gasoline and acetone, and applied to the carrier by generally known methods.
  • a suitable solvent for example toluene or mixtures of gasoline and acetone
  • melt processing these may be application methods via a die or calender.
  • coatings with doctor blades, knives, rollers or nozzles are known, to name but a few.
  • the PSA contains no longer volatile organic compounds (VOC) than 50 ⁇ g carbon per gram mass, in particular not more than 10 ⁇ g C / g, measured according to VDA 277.
  • VOC volatile organic compounds
  • the PSA can either be used for full-surface bonding of (opto) -electronic arrangements or, after suitable fabrication, diecuts, rolls or other shaped articles can be produced from the PSA or the PSA tape.
  • Corresponding diecuts and shaped bodies of the PSA / of the pressure-sensitive adhesive tape are then preferably adhesively bonded to the substrate to be bonded, for example as borders or delimitation of an (opto) electronic arrangement.
  • the choice of the shape of the stamped product or the molding is not limited and is chosen depending on the type of (opto) electronic arrangement.
  • the PSA is provided in the form of a planar structure with a carrier, it is preferred that the thickness of the carrier is in the range from about 1 ⁇ to about 350 ⁇ , more preferably between about 4 ⁇ and about 250 ⁇ and particularly preferably between about 12 ⁇ and about 150 ⁇ . The optimum thickness depends on the (opto) electronic arrangement, the end use and the type of execution of the PSA.
  • Very thin carriers in the range of 1 to 12 ⁇ are used in (opto) electronic structures that should achieve a low overall thickness, but it is the cost of integration into the structure increases.
  • Very thick carriers between 150 and 350 ⁇ m are used when an increased permeation barrier through the carrier and the rigidity of the structure are in the foreground; the protective effect is increased by the carrier, while the flexibility of the structure is reduced.
  • the preferred range between 12 and 150 ⁇ represents an optimal compromise as encapsulation solution for most (opto) electronic structures.
  • FIG. 1 shows a first (opto) electronic arrangement in a schematic representation
  • Fig. 3 shows a third (opto) electronic arrangement in a schematic representation.
  • FIG. 1 shows a first embodiment of an (opto) electronic arrangement 1.
  • This arrangement 1 has a substrate 2 on which an electronic structure 3 is arranged.
  • the substrate 2 itself is formed as a barrier for permeants and thus forms part of the encapsulation of the electronic structure 3.
  • another cover 4 designed as a barrier is arranged above the electronic structure 3, in the present case also spatially spaced therefrom.
  • a pressure-sensitive adhesive 5 is provided circumferentially next to the electronic structure 3 on the substrate 2.
  • the pressure-sensitive adhesive 5 connects the cover 4 to the substrate 2.
  • the pressure-sensitive adhesive 5 also allows the spacing of the cover 4 from the electronic structure 3 by means of a correspondingly thick embodiment.
  • the PSA 5 is one based on organometallic modified polymers, as described above in a general form and is set forth in more detail below in exemplary embodiments.
  • the PSA 5 not only performs the function of bonding the substrate 2 to the cover 4, but also provides a barrier layer for permeants so as to encapsulate the electronic structure 2 from the side against permeants such as water vapor and oxygen.
  • the PSA 5 is presently also provided in the form of a diecut from a double-sided adhesive tape. Such a punched product enables a particularly simple application.
  • Fig. 2 shows an alternative embodiment of an (opto) electronic device 1. Shown again is an electronic structure 3, which is arranged on a substrate 2 and encapsulated by the substrate 2 from below. Above and to the side of the electronic structure, the pressure-sensitive adhesive 5 is now arranged over its entire surface. The electronic structure 3 is thus encapsulated by the pressure-sensitive adhesive 5 at these points.
  • a cover 4 is then applied. In contrast to the previous embodiment, this cover 4 does not necessarily have to meet the high barrier requirements, since the barrier is already provided by the pressure-sensitive adhesive.
  • the cover 4 may, for example, only perform a mechanical protective function, but it may also be additionally provided as a permeation barrier.
  • FIG. 3 shows a further alternative embodiment of an (opto) electronic arrangement 1.
  • two pressure-sensitive adhesives 5a, b are now provided, which in the present case are of identical design.
  • the first pressure-sensitive adhesive 5a is arranged over the entire surface of the substrate 2.
  • the provided electronic structure 3 which is fixed by the pressure-sensitive adhesive 5a.
  • the composite of PSA 5a and electronic structure 3 is then completely covered with the further PSA 5b, so that the electronic structure 3 is encapsulated on all sides by the PSAs 5a, b.
  • the cover 4 is again provided.
  • neither the substrate 2 nor the cover 4 necessarily have barrier properties. However, they can nevertheless be provided to further restrict the permeation of permeants to the electronic structure 3.
  • the pressure-sensitive adhesive 5 is here and preferably applied in each case with a homogeneous layer thickness.
  • the transition is fluid and it may remain small un-filled or gas-filled areas.
  • the PSA is locally compressed to different degrees, so that by flow processes a certain compensation of the height difference can be made to the edge structures.
  • the dimensions shown are not to scale, but rather serve only a better representation.
  • the electronic structure itself is usually relatively flat (often less than 1 ⁇ thick).
  • the application of the PSA 5 takes place in all embodiments shown in the form of a pressure-sensitive adhesive tape.
  • This can basically be a double-sided pressure-sensitive adhesive tape with a carrier or a transfer adhesive tape.
  • an embodiment is selected as a transfer adhesive tape.
  • a polyethylene terephthalate (PET) and a polyethylene plate (PE) was used as a defined primer a steel surface.
  • PET polyethylene terephthalate
  • PE polyethylene plate
  • the glued surface element to be examined was cut to a width of 20 mm and a length of about 25 cm, provided with a handling section and immediately thereafter pressed five times with a steel roller of 4 kg at a feed rate of 10 m / min on the selected primer.
  • the previously bonded surface element at an angle of 180 ° at room temperature and at 300 mm / min was removed from the primer with a tensile tester (Zwick) and measured the force required for this purpose.
  • the measured value (in N / cm) was the average of three individual measurements.
  • a Caiciumtest was used as a measure of the determination of the life of an (opto) electronic structure. For this purpose, a 20 ⁇ 20 mm 2 large, thin calcium layer is deposited on a glass plate under a nitrogen atmosphere. The thickness of the calcium layer is about 100 nm.
  • an adhesive tape with the adhesive to be tested and a thin glass plate 35 ⁇ , Schott is used as a carrier material. The adhesive tape is applied with an all-round edge of 3 mm above the calcium level in which it adheres directly to the glass plate. Due to the impermeable glass carrier of the adhesive tape only the permeation is determined by the pressure-sensitive adhesive.
  • the test is based on the reaction of calcium with water vapor and oxygen, as described for example by AG Erlat et. al. in "47th Annual Technical Conference Proceedings Society of Vacuum Coaters", 2004, pages 654 to 659, and by ME Gross et al., in "46th Annual Technical Conference Proceedings Society of Vacuum Coaters", 2003, pages 89 to 92 are.
  • the light transmission of the calcium layer is monitored, which increases by the conversion into calcium hydroxide and calcium oxide. This takes place in the described test setup from the edge, so that the visible surface of the calcium level is reduced. It is the time to halve the area of the calcium level called lifetime.
  • As measuring conditions are 60 ° C and 90% relative humidity selected.
  • the samples were glued with a layer thickness of the PSA of 15 ⁇ full surface and free of bubbles.
  • the pressure-sensitive adhesives in Examples 1 to 3 were prepared from solution.
  • the individual components were dissolved in toluene (solids content 40%) and coated on an untreated 23 ⁇ PET film and dried at 120 ° C for 15 minutes, so that an adhesive layer with a basis weight of 50 g / m 2 was formed.
  • For the life test samples were prepared in the same way, but the coating was not carried out on a PET film but on a with 1, 5 g / m 2 siliconized release paper with a Klebmassetikdicke of 15 g / m 2 .
  • Tuftec P 1500 partially hydrogenated styrene-butadiene-styrene block copolymer with hydrogenated
  • Block polystyrene content 78 wt .-% diblock from Asahi
  • Tuftec P 1500 100 parts were dissolved in dry toluene to give a 20% solution. Subsequently, 1 part of tnmethoxyvinylsilane and 0.2 part of benzoyl peroxide are added. The solution is boiled for 2 h and then the polymer is precipitated in dry ethanol, washed with dry ethanol and dried at 60.degree.
  • Block polystyrene content without diblock and with 1, 7 wt .-%
  • Example 3 100 parts of Epofriend AT-501, an epoxidized SBS from Daicel, and 4 parts of Dynasylan 1122 (bis (3-triethoxysilyl-propyl) amine) are mixed in a melt kneader at 160 ° C. After the elastomer has melted homogeneously, 80 parts of Pentalyn H (Eastman's rosin ester) and 20 parts of Wingtack 10 (Cray Valley liquid C5 resin) are added.
  • Pentalyn H Eastman's rosin ester
  • Wingtack 10 Cray Valley liquid C5 resin
  • the adhesive is coated using a two-roll mill on a siliconized release paper with a coating weight of 50g / m 2 .
  • Block polystyrene content 36 wt .-% diblock and 1 wt .-%
  • Block polystyrene content without diblock and with 1, 7 wt .-%
  • This example is not a pressure sensitive adhesive but a hot melt adhesive that needs to be heated to stick. For the measurements it was heated for 5 s to 80 ° C during the gluing.
  • Tuftec P 1500 partially hydrogenated styrene-butadiene-styrene block copolymer having hydrogenated vinyl groups in the side chains with 30 wt .-% block polystyrene content, 78 wt .-% diblock from Asahi
  • Block polystyrene content 36 wt .-% diblock and 1 wt .-% maleic acid Kraton

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  • Chemical Kinetics & Catalysis (AREA)
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  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Electroluminescent Light Sources (AREA)
EP11779147.5A 2010-11-12 2011-10-27 Klebmasse und verfahren zur kapselung einer elektronischen anordnung Withdrawn EP2638570A1 (de)

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DE102010043871A DE102010043871A1 (de) 2010-11-12 2010-11-12 Klebmasse und Verfahren zur Kapselung einer elektronischen Anordnung
PCT/EP2011/068822 WO2012062587A1 (de) 2010-11-12 2011-10-27 Klebmasse und verfahren zur kapselung einer elektronischen anordnung

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Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102013202473A1 (de) 2013-02-15 2014-08-21 Tesa Se Verfahren zum Entfernen von Permeaten aus Flächengebilden
TW201436855A (zh) 2012-12-21 2014-10-01 Tesa Se 從平面結構物移除滲透物的方法
DE102012224319A1 (de) 2012-12-21 2014-06-26 Tesa Se Verfahren zum Entfernen von Permeaten aus Flächengebilden
DE102014200948A1 (de) 2014-01-20 2015-07-23 Tesa Se Verfahren zum Entfernen von Permeaten aus Flächengebilden
DE102014207837A1 (de) 2014-04-25 2015-10-29 Tesa Se Dünnglasverbund und Verfahren zur Lagerung von Dünnglas
DE102014207792A1 (de) 2014-04-25 2015-10-29 Tesa Se Dünnglasverbund und Verfahren zum Lagern einer Dünnglasfolie
US20160317068A1 (en) * 2015-04-30 2016-11-03 Verily Life Sciences Llc Electronic devices with encapsulating silicone based adhesive
US9960389B1 (en) 2017-05-05 2018-05-01 3M Innovative Properties Company Polymeric films and display devices containing such films
JP7238800B2 (ja) * 2018-01-31 2023-03-14 日本ゼオン株式会社 樹脂フィルム及び有機エレクトロルミネッセンス装置

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060235156A1 (en) * 2005-04-14 2006-10-19 Griswold Roy M Silylated thermoplastic vulcanizate compositions

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4051195A (en) 1975-12-15 1977-09-27 Celanese Polymer Specialties Company Polyepoxide-polyacrylate ester compositions
GB1552046A (en) 1977-02-02 1979-09-05 Ciba Geigy Ag Film adhesives
US5304419A (en) 1990-07-06 1994-04-19 Alpha Fry Ltd Moisture and particle getter for enclosures
US5290882A (en) * 1991-08-13 1994-03-01 Shin-Etsu Chemical Co., Ltd. Thermosetting resin compositions
EP0827994B1 (de) 1996-09-04 2002-12-18 Degussa AG Verwendung von silangepfropften amorphen Poly-alpha-Olefinen als feuchtigkeitsvernetzender Klebrohstoff oder Klebstoff
DE69627715T2 (de) 1996-11-12 2004-03-04 Minnesota Mining And Manufacturing Co., St. Paul Ein thermostatoplastischer vorläufer für einen druckempfindlichen klebstoff
DE69919004T2 (de) * 1998-08-21 2005-03-24 Hitachi Chemical Co., Ltd. Pastenzusammensetzung, schutzfilm und daraus hergestellte halbleitervorrichtung
JP3784202B2 (ja) * 1998-08-26 2006-06-07 リンテック株式会社 両面粘着シートおよびその使用方法
US7193594B1 (en) 1999-03-18 2007-03-20 Semiconductor Energy Laboratory Co., Ltd. Display device
JP2000311782A (ja) 1999-04-27 2000-11-07 Nec Corp 有機ｅｌディスプレイおよびその製造方法
DE19929011A1 (de) * 1999-06-25 2000-12-28 Bayer Ag Spezielle Aminosilane enthaltende, kondensationsvernetzende Polyurethanmassen, ein Verfahren zu ihrer Herstellung sowie ihre Verwendung
US6833668B1 (en) 1999-09-29 2004-12-21 Sanyo Electric Co., Ltd. Electroluminescence display device having a desiccant
US6664318B1 (en) * 1999-12-20 2003-12-16 3M Innovative Properties Company Encapsulant compositions with thermal shock resistance
CN1558921A (zh) 2001-08-03 2004-12-29 Dsm 显示器件用可固化组合物
US6936131B2 (en) 2002-01-31 2005-08-30 3M Innovative Properties Company Encapsulation of organic electronic devices using adsorbent loaded adhesives
KR20050037561A (ko) 2002-07-24 2005-04-22 어드헤시브즈 리서치, 인코포레이티드 가변형성 감압 접착 테이프 및 디스플레이 스크린에서의그 용도
JP4327489B2 (ja) 2003-03-28 2009-09-09 本田技研工業株式会社 燃料電池用金属製セパレータおよびその製造方法
CN101184809A (zh) * 2005-09-02 2008-05-21 信越化学工业株式会社 环氧树脂组成物以及包含该组成物的粘晶剂
JP2007197517A (ja) 2006-01-24 2007-08-09 Three M Innovative Properties Co 接着性封止組成物、封止フィルム及び有機ｅｌ素子
DE102006047738A1 (de) * 2006-10-06 2008-04-10 Tesa Ag Hitzeaktivierbares Klebeband insbesondere für die Verklebung von elektronischen Bauteilen und Leiterbahnen
DE102008047964A1 (de) * 2008-09-18 2010-03-25 Tesa Se Verfahren zur Kapselung einer elektronischen Anordnung
DE102008062130A1 (de) * 2008-12-16 2010-06-17 Tesa Se Verfahren zur Kapselung einer elektronischen Anordnung
US8222352B2 (en) * 2008-12-24 2012-07-17 Nitto Denko Corporation Silicone resin composition
DE102009036970A1 (de) * 2009-08-12 2011-02-17 Tesa Se Verfahren zur Kapselung einer elektronischen Anordnung
DE102009036968A1 (de) * 2009-08-12 2011-02-17 Tesa Se Verfahren zur Kapselung einer elektronischen Anordnung

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060235156A1 (en) * 2005-04-14 2006-10-19 Griswold Roy M Silylated thermoplastic vulcanizate compositions

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2012062587A1 *

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KR20130141588A (ko) 2013-12-26
CN103348465A (zh) 2013-10-09

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