WO2011020581A1 - Housing for electrical power cells in electrically driven automotive vehicles - Google Patents

Housing for electrical power cells in electrically driven automotive vehicles Download PDF

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Publication number
WO2011020581A1
WO2011020581A1 PCT/EP2010/004957 EP2010004957W WO2011020581A1 WO 2011020581 A1 WO2011020581 A1 WO 2011020581A1 EP 2010004957 W EP2010004957 W EP 2010004957W WO 2011020581 A1 WO2011020581 A1 WO 2011020581A1
Authority
WO
WIPO (PCT)
Prior art keywords
housing
thermoplastic polymer
support layer
layer
weight
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.)
Ceased
Application number
PCT/EP2010/004957
Other languages
English (en)
French (fr)
Inventor
Bernd Hoecker
Klaus Müller
Ines Schwarz
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.)
Basell Polyolefine GmbH
Original Assignee
Basell Polyolefine GmbH
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=42753394&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2011020581(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Basell Polyolefine GmbH filed Critical Basell Polyolefine GmbH
Priority to JP2012525078A priority Critical patent/JP5780559B2/ja
Priority to CN201080037340.1A priority patent/CN102548750B/zh
Priority to EP10742774.2A priority patent/EP2467253B1/en
Priority to ES10742774.2T priority patent/ES2661309T3/es
Priority to US13/390,684 priority patent/US9174417B2/en
Priority to BR112012003425A priority patent/BR112012003425B1/pt
Publication of WO2011020581A1 publication Critical patent/WO2011020581A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • B32B2307/306—Resistant to heat
    • B32B2307/3065—Flame resistant or retardant, fire resistant or retardant
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/50—Properties of the layers or laminate having particular mechanical properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/718—Weight, e.g. weight per square meter
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2457/00—Electrical equipment
    • B32B2457/10—Batteries
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2605/00—Vehicles
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2220/00—Batteries for particular applications
    • H01M2220/20—Batteries in motive systems, e.g. vehicle, ship, plane
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Definitions

  • the present invention relates to a novel housing suitable to comprise multiple electrical power cells in electrically driven motor vehicles.
  • the invention further relates to a process for production of said housing.
  • Housings comprising multiple of electrical power cells in motor vehicles are usually necessary to protect the electrical power cells arranged inside from outside influences. Vice versa the housings are suitable, as well, to protect any persons sitting in the car from any influences originated from the electrical power cells inside the housing which may be overheated or subjected to leakage.
  • Such housings are manufactured mainly from plastic material such as polyethylene or polypropylene by injection molding in different sizes and up to a volume of 1000 liters.
  • Such housings have at the one side the advantage that they are electrically insulating and that they are light in weight. However, at the other side they have the disadvantage that their mechanically strength is poor and that they are flammable at high temperatures or in case of fire.
  • the object of the present invention was therefore to provide a new housing for multiple of electrical power cells in motor vehicles which is light in weight, however, which has in combination therewith higher mechanical strength and, thus, provides protection for the power cells comprised therein against mechanical damages and which is inflammable and which provides at least partially protection for the power cells comprised therein against the influence of electromagnetic radiation.
  • a housing as mentioned initially comprising at least one lower receiving part and one upper covering part which fit together and can be closed to create inside a hollow space and which are prepared from a multilayered material comprising at least one support layer of thermoplastic polymer and at least one cover layer of metal adhering to each other.
  • the cover layer of metal may be arranged at the outer side of the housing or alternatively at the inner side of the housing. However, it is also possible to arrange the cover layer of metal either at the outer side of the housing and at the inner side of the housing.
  • the multilayered material comprising at least a support layer of thermoplastic polymer and at least a cover layer of metal permits the preparation of a housing perfectly suitable to incorporate therein multiple electrical power cells as they are used for electrically driven motor vehicles.
  • Such housing has nevertheless sufficient strength, especially also at large- surface area parts of the housing, such as the bottom, and also provides sufficient protection against immediate permeation of fire either from inside to outside or from outside to inside.
  • the stiffness of the housing can be markedly improved via lamination of the support layer with the cover layer of metal. For example, it is possible to achieve a stiffness level which hitherto has been unachievable via straight plastics-parts solutions for housing applications.
  • a good example being a housing composed of acrylonitrile-butadiene-styrene copolymer (ABS) known for its high stiffness. This applies particularly to such areas where the housings have exposure to relatively high temperatures in the motor vehicle.
  • ABS acrylonitrile-butadiene-styrene copolymer
  • the housing according to the instant invention leads to clear advantages here.
  • the mechanical strength of the housing can be further improved, if the cover layer of metal is arranged on both sides of the support layer.
  • the mechanical properties of the housing can be varied further within a particularly wide range by way of controlled modification of the support layer of thermoplastic polymer, which can be impact-modified, provided with mineral fillers, or glassfiber-reinforced, and the mechanical properties can thus be matched to the requirements placed upon the housing, without any resultant effect on the surface properties and the surface quality of the housing parts, either the lower receiving part and the upper cover part.
  • the support layer composed of thermoplastic polymer can comprise, based in each case on the weight of the support layer, from 1 to 60 % by weight, preferably from 5 to 50 % by weight, particularly preferably from 10 to 40 % by weight, of reinforcing fillers.
  • the lower backing layer can moreover also comprise respectively advantageous amounts of further additives, e.g. light stabilizers, UV stabilizers, heat stabilizers, pigments, carbon blacks, lubricants, and processing aids, flame retardants, blowing agents, and the like.
  • the lower backing layer itself is composed of thermoplastic polymers.
  • the thermoplastic polymers used with advantage for the support layer comprise polymers such as polypropylene (PP), polyethylene (PE), polyvinyl chloride (PVC), polysulfones, polyether ketones, polyesters, such as polyethylene terephthalate, polybutylene terephthalate or polyalkylene naphthalate, polycycloolefins, polyacrylates, polymethacrylates, polyamides, such as poly-epsilon-caprolactam or poly- hexamethyleneadipineamide or polyhexamethylenesebacineamide, polycarbonate, polyurethanes, polyacetals, such as polyoxymethylene (POM) or polystyrene (PS).
  • PP polypropylene
  • PE polyethylene
  • PVC polyvinyl chloride
  • polysulfones polyether ketones
  • polyesters such as polyethylene terephthalate, polybutylene terephthalate or polyalkylene naphthalate
  • Thermoplastic polymers principally suitable here are homopolymers and copolymers.
  • copolymers composed of propylene and ethylene or composed of ethylene or propylene and of other olefins having from 4 to 10 carbon atoms are particularly worthy of mention, as are co- or terpolymers composed of styrene and of relatively small proportions of butadiene, alpha- methylstyrene, acrylonitrile, vinylcarbazole, or esters of acrylic, methacrylic, or itaconic acid.
  • its upper covering part can also comprise amounts of up to 60 % by weight, based on the total weight of the upper covering part, of reclaimed materials recycled from the polymers mentioned.
  • polyoxymethylene means homo- and copolymers of aldehydes, such as formaldehyde or acetaldehyde, but preferably of cyclic acetals.
  • a characteristic of POM is that there are constantly recurring carbon-oxygen bonds forming a distinctive feature of the molecular chain.
  • the melt flow index (Ml) of POM is usually in the range from 5 to 50 g/10 min, preferably from 5 to 30 g/10 min, measured to ISO 1133 at a temperature of 230 0 C with a load of 2.16 kg.
  • polyester for the support layer of the housing
  • materials clearly preferable for this purpose are polyethylene terephthalate
  • the Ml of particularly suitable polyesters is in the range from 5 to 50 g/10 min, preferably from 5 to 30 g/10 min, measured to DIN 1133 at a temperature of 230 0 C with a load of 2.16 kg.
  • Copolymers of styrene that can be used for the support layer of the housing are in particular copolymers having up to 45 % by weight, preferably having up to 20 % by weight, of acrylonitrile within the polymer.
  • the Ml of these copolymers is typically in the range from 1 to 25 g/10 min, preferably from 4 to 20 g/10 min, measured to DIN 1133 at a temperature of 230 0 C with a load of 2.16 kg.
  • Further terpolymers of styrene comprise up to 35 % by weight, in particular up to 20 % by weight, of acrylonitrile within the polymer and up to 35 % by weight, preferably up to 30 % by weight, of butadiene.
  • ABS is also used for these terpolymers, whose Ml is typically in the range from 1 to 40 g/10 min, preferably from 2 to 30 g/10 min, measured to DIN 1133 at a temperature of 230 0 C with a load of 2.16 kg.
  • thermoplastics used for the support layer of the housing are in particular polyolefins, such as polyethylene (PE) and polypropylene (PP), among which particular preference is given to use of PP.
  • PE polyethylene
  • PP polypropylene
  • PP means homo- and copolymers of propylene.
  • Copolymers comprise subordinate amounts of monomers copolymerizable with propylene, e.g. 1 -olefins having 2 or 4 to 8 carbon atoms. If necessary, it is also possible to use two or more comonomers.
  • Thermoplastics which may be mentioned as particularly suitable for the support layer of the housing are homopolymers of propylene or copolymers composed of propylene and up to 50 % by weight of further 1 -olefins having up to 8 carbon atoms. These copolymers are normally random copolymers, but can also be block copolymers.
  • the polymerization reaction for production of PP can normally take place at a pressure in the range from 1 to 100 bar (from 0.1 to 10 MPa) in suspension or in the gas phase and in the presence of a Ziegler-Natta catalyst system.
  • catalyst systems which comprise not only a titanium-containing solid component but also co- catalysts in the form of organoaluminum compounds and electron-donor compounds.
  • Ziegler-Natta catalyst systems generally comprise a titanium-containing solid component, in particular halides or alcoholates of tri- or tetravalent titanium, and moreover a halogen-containing magnesium compound, inorganic oxides, such as silica gel, as support material, and electron-donor compounds.
  • a titanium-containing solid component in particular halides or alcoholates of tri- or tetravalent titanium
  • a halogen-containing magnesium compound such as silica gel
  • electron-donor compounds are carboxylic acid derivatives or ketones, ethers, alcohols, or organosilicon compounds.
  • the titanium-containing solid component can be prepared by known processes. It is preferably prepared by a process described in more detail in DE 195 29 240.
  • Co-catalysts suitable for the Ziegler-Natta catalyst systems are not only trialkylaluminum compounds but also compounds in which an alkyl group has been replaced by an alkoxy group or by a halogen atom, such as chlorine or bromine.
  • the alkyl groups can be identical or different. Linear or branched alkyl groups can also be used. According to the invention, it is preferable to use trialkylaluminum compounds whose alkyl groups comprise from 1 to 8 carbon atoms, examples being triethylaluminum, triisobutylaluminum, trioctylaluminum, or methyldiethylaluminum, or a mixture thereof.
  • PP can also be produced in the presence of metallocene as catalyst.
  • Metallocenes are complex compounds having a layered structure and comprising metals from the transition groups of the Periodic Table of the Elements plus organic, preferably aromatic, ligands.
  • the metallocene complexes are advantageously applied to a support material.
  • Support materials which have proven advantageous are the inorganic oxides also used for preparation of the titanium-containing solid component in Ziegler-Natta catalysts.
  • Metallocenes usually used comprise, as central atom, titanium, zirconium, or hafnium, among which zirconium is preferred.
  • the central atom has pi- bonding to at least one pi system, which is embodied by a cyclopentadienyl group.
  • the cyclopentadienyl group has additional substituents, which can be used to control the activity of the catalyst.
  • Preferred metallocenes comprise central atoms bonded by way of two similar or different pi-bonds to two pi-systems, and these may also simultaneously be a constituent of appropriate heteroaromatic systems.
  • a suitable co-catalyst for the metallocene is in principle any compound which can convert the neutral metallocene to a cation and can stabilize the metallocene. Furthermore, as can be found in EP 427 697, the cocatalyst or the anion formed therefrom should not enter into any further reactions with the metallocenium cation formed.
  • the cocatalyst used is preferably an aluminum compound and/or a boron compound.
  • the formula of the boron compound is preferably R 18 xNH 4- ⁇ BR 19 4 ,R 18 x PH 4- ⁇ BR 19 4 ,R 18 3 CBR 19 4 ) or BR 19 3 , in which x is a number from 1 to 4, preferably 3, the radicals R 18 are identical or different, preferably identical, and are Ci-Cio-alkyl or C 6 -Cis-aryl, or two radicals R 18 together with the atoms connecting them form a ring, and the radicals R 19 are identical or different, preferably identical, and are C ⁇ -Cis-aryl, which can be alkyl, haloalkyl, or fluorine substituted.
  • R 18 is ethyl, propyl, butyl, or phenyl
  • R 19 is phenyl, pentafluorophenyl, 3,5- bistrifluoromethylphenyl, mesityl, xylyl or tolyl.
  • EP 426 638 describes boron compounds as cocatalyst for metallocenes.
  • the co-catalyst used is an aluminum compound, such as alumoxane and/or an alkylaluminum compound. It is particularly preferable that the co-catalyst used is an alumoxane, in particular of linear type or of cyclic type, and in both of the compounds here there can also be organic radicals present which are identical or different and can be hydrogen or a Ci-C 2 o-hydrocarbon group, such as a C 1 -Ci 8 - alkyl group, a C 6 -Ci 8 -aryl group, or benzyl.
  • the support layer of the housing together with the cover layer of metal can take the form of injection-molded, extruded, or compression-molded sheet in various thicknesses and sizes.
  • Preferred layer thicknesses for the support layer are in the range from 1 to 20 mm, particularly preferably from 2 to 15 mm.
  • For the cover layer of metal different metals are useful. Thus, aluminum is very suitable, but also iron is useful or noble metals like silver or chromium, whereby aluminum, iron or chromium are preferred.
  • the thicknesses of the cover layer of metal is in the range of 50 to 1000 ⁇ m, preferably in the range of from 70 to 500 ⁇ m.
  • an additional intermediate layer may be arranged between the support layer of thermoplastic polymer and the cover layer of metal to improve the adhesion strength of the two layers.
  • a particular material that can be used for the intermediate layer is a thermoplastic polymer, preferably the same thermoplastic polymer as that used for the support layer. This combination can produce a particularly firmly adhering bond between the support layer and the cover layer of metal.
  • the intermediate layer is in the form of a thin web or else, preferably a thin nonwoven, with thickness in the range from 0.001 to 1 mm, preferably from 0.005 to 0.5 mm.
  • thermoplastic material preferably used for the intermediate layer is a PP which has been produced in the presence of metallocene as catalyst and whose Ml is in the range from 10 to 60 g/10 min, measured to DIN 1133 at a temperature of 230 0 C with a load of 2.16 kg.
  • the intermediate layer composed of thermoplastic polymer can also with high advantage be a resin-saturated nonwoven.
  • Acrylate resins, phenolic resins, urea resins, or melamine resins may in particular be used here as saturating resin.
  • the degree of saturation with resin here can be up to 300 %, and this means that practically the entire surface of the intermediate layer has been heavily saturated with resin, which then amounts to 300 % of the weight of the intermediate layer without resin.
  • the degree of saturation with resin is preferably from 15 to 150 %, particularly preferably from 80 to 120 %.
  • the weight of the intermediate layer is in the range from 15 to 150 g/m 2 , preferably from 30 to 70 g/m 2 .
  • the invention also provides a process for production of the housing by the technique of reverse coating by an injection-molding method.
  • the initial charge in the technique of reverse coating by an injection-molding method places the material for the intermediate layer and the cover layer of metal on one of the sides into one half of an injection mold, and, where desired, the material for an intermediate layer and another cover layer of metal on the other side into the other half of the injection mold.
  • the mold temperature is generally from 8 to 160 °C on each side.
  • a prefabricated laminate comprising the intermediate layer and a metal foil whose layer thickness is in the range from 0.02 to 20 mm or, as an alternative to this, individual foils (overlay, metal, resin) are first laminated to a nonwoven (about 30 g/m 2 ; metallocene polymer, ®Novolen). Material for a further prefabricated laminate is then prefabricated with the desired thickness and shape.
  • the two variants are then placed in the respective opposite mold halves of an injection-molding compartment, the mold is closed, and then the thermoplastic is injected using a temperature of at least 170 0 C and a pressure of at least 50 bar (5 MPa) between these, into the compartment.
  • thermoplastic polymer for the support layer is introduced in the form of pellets between the individual foils inserted in the layer sequence, and is exposed to pressure of at least 5 bar and to a press temperature of at least 100 0 C on each side, for a press time period of at least 30 sec.
  • the housing for the electrical power cells comprises inside a volume of in the range of from at least 1 liter up to about 1000 liters in maximum, preferably from 1 ,5 liters to about 800 liters.
  • the lower receiving part and the upper covering part of the housing fit thereby together like tongue and groove joint and are connected with each other by screwing both parts together or clamping them together.
  • Figure 1 shows a vertical cut through a part of a housing from side view having the cover layer of metal arranged at the outer side of the housing.
  • Reference numerals indicate where the cover layer of metal 1 is to see comprising an aluminum foil and where the support layer 2 of talcum reinforced PP is to see.
  • Figure 2 shows another vertical cut through another version of the housing in sandwich structure in side view. This version using a support layer having arranged cover layers on both sides.
  • the reference numerals in figure 3 indicate the support layer 2 comprising PP and covered on both sides with cover layers 1 containing aluminum foils.

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  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Electrochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Composite Materials (AREA)
  • Materials Engineering (AREA)
  • Textile Engineering (AREA)
  • Laminated Bodies (AREA)
  • Battery Mounting, Suspending (AREA)
  • Injection Moulding Of Plastics Or The Like (AREA)
PCT/EP2010/004957 2009-08-18 2010-08-12 Housing for electrical power cells in electrically driven automotive vehicles Ceased WO2011020581A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP2012525078A JP5780559B2 (ja) 2009-08-18 2010-08-12 電気的に駆動される自動車の電池用ハウジング
CN201080037340.1A CN102548750B (zh) 2009-08-18 2010-08-12 用于电力驱动的机动车辆中的电源电池的外壳
EP10742774.2A EP2467253B1 (en) 2009-08-18 2010-08-12 Housing for electrical power cells in electrically driven automotive vehicles
ES10742774.2T ES2661309T3 (es) 2009-08-18 2010-08-12 Compartimento para baterías eléctricas en vehículos automotores eléctricos
US13/390,684 US9174417B2 (en) 2009-08-18 2010-08-12 Housing for electrical power cells in electrically driven automotive vehicles
BR112012003425A BR112012003425B1 (pt) 2009-08-18 2010-08-12 alojamento apropriado para compreender múltiplas células de energia elétrica em veículos automotivos acionados eletricamente

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP09010595 2009-08-18
EP09010595.8 2009-08-18
US27487609P 2009-08-21 2009-08-21
US61/274,876 2009-08-21

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Publication Number Publication Date
WO2011020581A1 true WO2011020581A1 (en) 2011-02-24

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US (1) US9174417B2 (https=)
EP (1) EP2467253B1 (https=)
JP (1) JP5780559B2 (https=)
KR (1) KR20120052990A (https=)
CN (1) CN102548750B (https=)
BR (1) BR112012003425B1 (https=)
ES (1) ES2661309T3 (https=)
WO (1) WO2011020581A1 (https=)

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EP2467253B1 (en) 2018-02-21
CN102548750B (zh) 2016-01-20
US9174417B2 (en) 2015-11-03
JP2013502674A (ja) 2013-01-24
EP2467253A1 (en) 2012-06-27
KR20120052990A (ko) 2012-05-24
US20120148892A1 (en) 2012-06-14
JP5780559B2 (ja) 2015-09-16
CN102548750A (zh) 2012-07-04
BR112012003425B1 (pt) 2019-12-17
BR112012003425A2 (pt) 2017-02-21

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