CN100427336C - Seating system and method of forming same - Google Patents
Seating system and method of forming same Download PDFInfo
- Publication number
- CN100427336C CN100427336C CNB2004800037655A CN200480003765A CN100427336C CN 100427336 C CN100427336 C CN 100427336C CN B2004800037655 A CNB2004800037655 A CN B2004800037655A CN 200480003765 A CN200480003765 A CN 200480003765A CN 100427336 C CN100427336 C CN 100427336C
- Authority
- CN
- China
- Prior art keywords
- amine
- base plate
- reinforcing member
- adhesives
- seat
- 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.)
- Expired - Fee Related
Links
Images
Landscapes
- Body Structure For Vehicles (AREA)
Abstract
The present invention discloses a seating system that includes a seat back (20) with one or more plastic panels (22) that extend across a lateral distance of the seat back (20). The seat back (20) preferably includes one or more reinforcements (30) attached to the plastic panels (22).
Description
The claim of date of application
The present invention was required on February 13rd, 2003, and U.S. provisional application sequence number is on January 13rd, 60/447,118 and 2004, and the U.S. patent application serial numbers is 10/755,897, the rights and interests of application.The two is merged reference at this for various purposes.
Technical field
The present invention relates to a kind of seat system of improvement, particularly relate to a kind of improvement seat system that is used for self-propelled vehicle.The invention still further relates to the automotive vehicle interior systems of improvement.
Background technology
The demand of improvement automotive vehicle seat system strengthens day by day.The automobile of hatch back is being arranged, and sport utility vehicle and benefit today of popularizing small-sized box type vehicle day, adjustable seat and in most cases suppress the needs that goods moves to motor vehicle rear has proposed the unique design challenge to automotive vehicle seat system.Consider that these vehicle are mainly used in goods together with passenger's (especially passenger in the back seat) loading with transport, the builder has turned to attention the performance of improvement seat system, makes it have higher weight capacity.
In order to improve weight capacity, can use one or more strenthening members in the seat system.Except that load-bearing property, need use cheaply material and line flow procedure to keep low cost.Therefore, embodiments of the present invention will be sought the seat reinforcement means that uses low-cost member.The making of member can be adopted assembly period, cost of equipment, the technology that labor cost is all lower.
There is multiple suitable improvement seat system to be disclosed, as: USP6,491,346 and the U.S. application sequence number be respectively: 09/766,792 (application on January 22 calendar year 2001), 60/312,874 (applications on August 15 calendar year 2001), 60/329,187 (application on October 12 calendar year 2001), 09/766,792 (application on January 22 calendar year 2001), 10/216,970 (applications on August 12nd, 2002), 60/414,040 patents such as (applications on September 27th, 2002) will be with reference to these correlation techniques in this patent.
Summary of the invention
The demand of prior art satisfies by a kind of automotive vehicle seat system provided by the invention, it comprises: a plastic seat backrest, back of seat has a base plate at least, and this base plate is limited by peripheral boundary and has between whole peripheral boundary a main wall of crossing over continuously basically.This at least one base plate comprises that one or more strenthening member is to strengthen the intensity of back of seat.According to a particularly preferred embodiment, the strenthening member on the base plate comprises the reinforcing member that an another kind of material of usefulness is made.Though reinforcing member can adopt multiple another kind of material to make, preferred material is a metal, and especially preferred material is a steel.
Though can adopt other method, preferably adopt technology for moulding to make seat back panel.In addition, in a particularly preferred embodiment, use adhesives that reinforcing member is appended on the back of seat.In this particularly preferred embodiment, back of seat can adopt various material to make, but preferred plastic material, more preferably the polypropylene material is more preferably glass fibre filled polypropylene material.
Place a 36kg weight at least behind back of seat, when acceleration/accel arrived 30g up to 20, seat system of the present invention can be not chipping.This system is easy to produce, and comprises an easy bonded assembly reinforcing member, thereby can reduce the cost of manufacture of back of seat.
Description of drawings
Fig. 1 is the transparent view that applies back of seat in the reinforcing member process;
Fig. 2 A is the cutaway view that applies Fig. 1 in the reinforcing member process;
Fig. 2 B is the cutaway view that applies Fig. 1 behind the reinforcing member;
Fig. 3 is that another applies the transparent view that adds back of seat in the member process.
The specific embodiment
The invention provides a kind of seat back system that comprises a strenthening member at least, particularly comprise the seat back system of the strenthening member that the auxiliary material of one or more employing is made.Preferably, reinforcing member along seat back panel a main wall extend.According to the present invention, the reinforcing member of being made by suitable material (for example metal) is easy to connect (for example adhesion) to the back of seat of being made by another kind of suitable material, but the connection of these two kinds of materials before is quite difficult.
Fig. 1, shown in 2A and the 2B is a kind of seat back system 20 of improvement, this seat back system 20 typically comprises: one or more base plate 22 (for example 60/40 five equilibrium, whole seat etc.), it crosses over the transverse distance of seat back system.Preferably, each base plate 22 comprises a main wall 26, below only to main wall 26 detailed descriptions in addition.
Seat back panel comprises one or more strenthening member (for example reinforcing member, timber, combination of the two or the like), and it is connected to and stretches out main wall to small part.Preferably, the main wall of each base plate is crossed over the periphery at this base plate basically continuously, and has strenthening member and prolong main wall basically and stretch.Preferably, strenthening member comprises that at least an employing is different from the strenthening member that the another kind of material of main wall is made.Yet strenthening member also can adopt the material close or identical with main wall or back of seat to make.Here the another kind of material of the Cai Yonging composition that is meant a kind of material or material and the chemical composition of back of seat material have at least slightly little different.
Seat back panel can be made by the material of any appropriate, includes but not limited to metal, plastics (strengthen or nonreinforcement plastics all can), other composite or the like.Preferably, a base plate will be arranged at least is plastics.More preferably, all base plates all are plastics (thermoplastic plastic for example, thermoset material or its combination).
According to the present invention, strenthening member comprises that one or more is different from the strenthening member that the material of base plate is made by composition or structure.
The application of microcellular foam also falls within the scope of the present invention.Corresponding with it, a kind of ready-made gas/polymer solution, refining and then nucleation are micropore under astable thermodynamic condition.Can control the growth of nucleon as required.
The making of seat back panel can be adopted the existing manufacturing technology of selected material, and for example forming work is moulded, machined into or other method, thus base plate is processed into required form.When base plate is plastic material, can adopt any suitable plastic manufacturing technology, include but not limited to: injection moulding (including but not limited to outside or inner gas injection method of molding), blow moulding, compression molding, rotomoulding, hot-forming method, extrude vacuum forming, foaming or the like.Also can adopt one or more other manufacturing technologies, insert molding for example, outer molded (over-molding) or its combination.Therefore, as previously mentioned, in one embodiment, utilize the advantage of unlike material and different manufacturing technologies, and help designing additional properties, can produce the mixed type seat unit.
The present invention proposes the use of strenthening member, to strengthen the rigidity of back of seat device, toughness and erosion-resisting characteristics, or the bending moment of local improvement member.
The structure or the pattern of strenthening member comprises " C " shape, " D " shape, " H " shape, " I " shape, " J " shape, " L " shape, " M " shape, " N " shape, " O " property, serpentine, "T"-shaped, " U " shape, " V " shape, " W " shape, " X " shape, " Y " shape, " Z " shape, curvilinear figure (for example sine curve), in a zigzag, "+" shape or the like.
In one embodiment, the jacking of floor member is made by another kind of material, and is connected to the strenthening member on the back of seat.Seat back panel strenthening member should require process according to the reinforcing of main wall, and this processing mode then depends on the back of seat design (for example shape, size, requirement of strength or the like) of concrete self-propelled vehicle.According to the designing requirement of back of seat, strenthening member can be or is smooth, or bending, or big, or little, or short, or long.In addition, strenthening member quantity how much depend on concrete needs or requirement.
In a highly preferred embodiment, strenthening member comprises one or more strenthening member, as the timber of being made by a whole material.As an example, timber can be solid or the groove shape structure, and is connected on the main wall of back of seat.Preferably, for the groove shape timber, it can adopt the gas injection method of molding described in the patent 60/414,040 (application on September 27th, 2002) to make
Fig. 1, shown in 2A and the 2B is the seat back system 20 that comprises a strenthening member 30 at least, described member has a reinforcing member 32 to be connected on the base plate 22.Preferably, reinforcing member 32 is made of another kind of material at least in part.
Reinforcing member 32 can be made into different shape and structure.For example, according to the application and the reinforcing mode of ruggedized equipment 32 in the backrest system 20, strenthening member can be flat, or crooked, or elongated, or short and thick, or how much, or other shape.In a specific implementations, reinforcing member 32 is that a length is L, and width is W, and thickness is that the thin bending of T is rectangular.Length wherein, width and thickness all are normal values, and these sizes change with the difference of strenthening member, and this size also can change because of single reinforcing key.
In general, the size of reinforcing member 32 is not limited by strictness, and it can be depending on the distance or the area of reinforcing member 32 required leaps.Yet, usually be keep reinforcing member 32 little size, especially thickness should be as far as possible little to alleviate its weight.Preferred thickness should be less than about 5mm, more preferably, and less than about 2mm, most preferably, less than about 1mm.For alleviating the weight of reinforcing member 32, one or more spaces (for example through hole) are arranged preferably on it.In this embodiment, for the hollow space that makes reinforcing member 32 occupies larger volume, reinforcing member is skeleton structure basically.
Preferably, but do not require, comprise on the reinforcing member 32 one with seat back system 20 base plates 22 on the surface 36 that is complementary, surface 40.Comprise on the reinforcing member 22 shown in Fig. 1-2 B that a pair of length is the timber 50 of L, with a connecting panel 52 that is connected timber 50, thereby form surface 36, it comprises a flat 54 and a pair of groove 56.Accordingly, a pair of reinforcing member 60 that the match surface 40 on seat back system 20 base plates 22 limits inserts groove 52, and par 64 matches with the par 54 of reinforcing member 32 is identical substantially.
The another kind of material of reinforcing member 32 can be selected from various material, as poly-mer, and glass, metal, fiber (for example glass, carbon fiber, aromatic poly amide metal (aramid metal) or the like), the braiding material, non-braiding material, and their compound or the like.One preferred embodiment in, described another kind of material is at least a portion or all is one or more metals basically, aluminium for example, iron, tungsten, magnesium, steel, tin, copper, titanium, alloy or the like.According to the described another kind of material of a preferred implementation is dead-soft steel basically fully.
The making of reinforcing member 32 can be adopted various manufacturing technologies, and as roll extrusion, casting is dashed and rolled or the like.Also can adopt mold, fabrication techniques such as extrude.
Suitable base plate can comprise a kind of plastic molded articles.Plastic material preferably includes a kind of homopolymer, as polyolefin, polyamide, polyphenylene oxide (polyphenylene oxide) and polystyrene, or a kind of copolymer with low-surface-energy, as polyalkylene terephthalate (polyalkylene terephthalate), copolymer also may have high surface energy.
Preferred plastic material comprises polypropylene, polyamide, polyamide alloy, polyphenylene ether polymer, polyphenylene oxide alloy, poly styrene polymer, polystyrene alloy, polybutylene terephthalate poly-mer and polybutylene terephthalate alloy.Can contain fiber in the plastic material, as short glass fiber, long glass fibres, short natural fiber or the right fiber of the vast of heaven.
Particularly preferred plastic material comprises the polypropylene of having filled short glass fiber, has filled the polypropylene of long glass fibres, has filled the polyamide and the polyamide alloy of having filled glass of glass.Particularly preferably be used for comprising the polypropylene of non-filler, filled the polypropylene of mica, filled the polypropylene of mineral as the plastic material of EAU buffer system.
At some preferably in the embodiment, can fiberfill fibers in the polymerizable material to gain in strength.Though can use the fiber of various sizes (for example length), and discover that fiber is long more, the intensity that increases is high more relatively.Therefore, in a preferred embodiment, polymerizable material is as ABS, PCABS, polypropylene, SMA (phenylethylene-maleic anhydride), PPO (polyphenylene oxide) or other suitable plastic are filled with glass fibre, its mean length approximately surpasses 2mm's, more preferably approximately surpass 4mm, the about 6mm of surpassing that is more preferably, most preferred greatly between 8-20mm.
Be to form strenthening member 30, reinforcing member 32 and seat back system 20 other parts be connected or integrated, can adopt various connections or integrated technology, as spiral nail, clasp, rivet, their combination or the like mechanical fastener.In addition, the manufacturing technology of having mentioned before the employing, reinforcing member 32 is moulded in the relevant position on seat back system 20 at least, the two can be integrated.Reinforcing member 32 is connected with base plate 22, also can adopt heat stake (heat staking), Vibration Welding, sonic welded, their technology such as combination.
In one embodiment, adopt adhesives 66 that reinforcing member 32 is adhered on the base plate 22 of seat back system 20.Preferably, adhesives 66 is applied to respectively in the match surface 40,36 of base plate 22 and reinforcing member 32 one or two.With surface 40 and 36 mutual extrusion, be about to reinforcing member 32 and connect together then with base plate 22.Certainly adhesives 66 is applied on the arbitrary surfaces of reinforcing member 32 or seat back system 20, then the two is bonded together.
Can adopt the adhesives of any appropriate among the present invention.Preferred adhesive 66 compatible with the material of base plate 22 and reinforcing member 32 (that is, be easy to bonding).If adhesives 66 with wherein a kind of material is incompatible, then needs the base plate of being made by incompatible material 22 or the surface of reinforcing member 32 are handled.The representative type processing method comprises application of primer, plasma radiation, the combination of the two etc.
In one embodiment, adhesives is based on the adhesives of urethanes, preferably urethane adhesive (for example polyurethane binder).Alternatively, can comprise a kind of function ingredients in this adhesives, be selected from methyl methacrylate (MMA), acrylonitrile-butadiene-styrene (ABS), polycarbonate (PC), or their compound (for example PC-ABS).In further for the embodiment that selects, adhesives is a silane adhesive, silicone adhesive or their compound.In another embodiment, adhesives is an acryloid cement.Adhesives can also be an epoxy radicals, can comprise polyolefins (polyolefinics), phenylethylene (styrenics), acrylic compounds (acrylics) or their compound.And in another embodiment, preferred adhesive comprises alkyl borane.USP09/466, the issue of 321 (applications on December 17th, 1999) and patent number is respectively: all announced the suitable bonding example in 20020058764 and 20030001410 the patent.Contain suitable modifier in these adhesivess, comprise tackifier, elastic body, impact modifier etc.
In a particularly preferred embodiment, be secure bond reinforcing member 32 and base plate 22, adopted organo-borane/amine complex adhesives or other adhesives of two components.Be found, this adhesives and metal (for example steel) and plastics, especially polypropylene are compatible.Like this, can directly use this adhesives to connect reinforcing member 32 that is made of metal and the seat back system of making by plastics or polypropylene 20, and need not the surface of preoperative treatment reinforcing member 32 or seat back system 20.
A particularly preferred embodiment of the present invention a kind of filling by molding is provided glass polypropylene and/or filled the base plate that the polyamide of glass is made, its surface energy is lower than 45mJ/m
2With a kind of by steel, the reinforcing member that zinc and/or aluminium are made.Like this, preferred adhesive is to be suitable for connecting surface energy to be lower than 45mJ/m
2The adhesives of bottom is applied to it on match surface, the two can be bonded together.This adhesives is a kind of following polymerisable composition generation that has, and this composition comprises:
I) a kind of organo-borane/amine complex;
Ii) one or more have the undersaturated monomer of ethylene linkage, oligomer or poly-mer, and it can be by the free radical polymerization polymerization; And can choose wantonly
Iii) a kind of described complex is separated,, have the polymeric compounds of undersaturated one or more monomers of ethylene linkage, oligomer or poly-mer with initiation to discharge borine.
Especially particularly preferred aspect of the present invention is the use of adhesives in foregoing self-propelled vehicle assembly production method and the fitting process.
The adhesives that proposes among the patent PCT/US00/33806 and and polymerizable composition be highly suitable for the present invention, so that structural elements and strenthening member are bonded together.
The amine that cooperates organoborane compounds, any can cooperation, the amine that can when separating the association medium and exist, separate again with organo-borane.Preferred amine comprises as Zharov at patent USP5, the 41-53 of the 5th row is capable in 539,070, and Skoultchi is at patent USP5,106, capable and the Pocius of 29-58 of the 2nd row is in patent USP5,686 in 928,29 of the 7th row walk to the primary amine that proposes in 36 row of the 10th row in 544, secondary amine contains the polyamine of primary amine or secondary amine group or ammonia; Monthanolamine, secondary dialkyl group diamines or polyoxyalkylene polyamine; Deviny is at patent USP5, in 883,208 30 of the 7th row walk to the diamines that proposes in 56 row of the 8th row with have two or more can with the amine end capping reaction product of the cmpd of the group of amine reaction.About the described resultant of reaction of Deviny, preferred di-primary amine (diprimary amines) comprises alkyl diprimary, aryl diprimary, alkylaryl di-primary amine and polyoxyalkylene diamines; Contain two or more carboxylic acids, carboxylate, carboxylic acid halide, aldehyde, epoxide, the cmpd of pure and mild acrylate group described can comprising with the cmpd of amine reaction.Preferred amine comprises n-octyl amine, 1, and 6-diamino hexane (1, the 6-hexamethylenediamine), diethylamine, dibutylamine, diethylene triamine, dipropylenediamine, 1,3-trimethylene diamine (1, the 3-propane diamine), 1, the 2-trimethylene diamine, 1,2-ethylene diamine, 1,5-pentanediamine, 1,12-docecane diamines, 2-methyl isophthalic acid, 5-pentanediamine, the 3-methyl isophthalic acid, 5-pentanediamine, trien, diethylene triamine.Preferred polyoxyalkylene polyamine comprises the polyethylene oxide diamines, PPO, triethylene glycol (TEG) trimethylene diamine, PolyTHF diamines and poly-
Epoxyethane copolymerization epoxypropane diamines.
Especially, the amine in organo-borane/amine complex can be selected from the amine with amidine structural constituent; Have the aliphatics heterocycle of at least one nitrogen in heterocycle, wherein this heterocyclic compound also can have one or more nitrogen-atoms in heterocycle, oxygen atom, sulphur atom or two key; Additional have one or more hydrogen bonds to accept the primary amine of group, wherein accepts that at primary amine and hydrogen bond two carbon atoms will be arranged between the group at least, preferably has three carbon atoms at least, the intensity of intermolecular or molecule interior effect can increasing B--N key in the complex; Or conjugated imines.
Preferred hydrogen bond is accepted group and is comprised: primary amine, secondary amine, tertiary amine, ether, halogen, polyethers or polyamine.Described heterocycle is the cmpd that contains one or more alicyclic rings, contains nitrogen on one of them ring.Described amidine or conjugated imines can be straight chain, side chain or ring-type.
Preferred organo-borane is trialkylborane or alkyl-cycloalkyl borine in the complex.This borine preferably has molecular formula 1:
B--(R
1)
3Molecular formula 1
Wherein: B is a boron; R
1Be a C
1-10Alkyl, C
3-10Naphthenic base, or by two or more R
1The alicyclic ring of be combined into.
Preferred R
1Be C
1-4Alkyl, even more preferably C
2-4Alkyl, most preferably C
3-4Alkyl.Preferred organo-borane comprises boron triethyl, triisopropyl borine and three normal-butyl borines.
One preferred embodiment in, the amine in the complex is accepted the cmpd of group by containing a primary amine and one or more hydrogen bond, wherein accepts that at primary amine and hydrogen bond two carbon atoms will be arranged between the group at least, preferably has three carbon atoms at least.
Preferably, this amine has molecular formula 2:
NH
2(CH
2)
b(C (R
2)
2)
aX molecular formula 2
Wherein: R
2Be hydrogen, C
1-4Alkyl or C
3-10Naphthenic base; X is that half hydrogen bond is accepted group; A is an integer between 1 and 10; B is 0 or 1, and a and b sum are between 2 and 10.
Preferred R
2Be hydrogen or methyl.
Preferred X is that half hydrogen bond is accepted group, and when hydrogen bond was accepted group and is amine, preferred X was a tertiary amine or secondary amine.Preferred X is--N (R
8) e,--OR
10, or halogen, wherein: R
8Be C
1-10Alkyl, C
3-10Naphthenic base or-(C (R
2)
2)
d--W; R10 is C
1-10Alkyl, C
3-10Naphthenic base or-(C (R
2)
2)
d--W; E equals 0,1 or 2.The X that is more preferably is--N (R
8)
2Or--OR
10
Preferred R
8And R
10Be C
1-4Alkyl or--(C (R
2)
2)
d-W, even more preferably C
1-4Alkyl, most preferably methyl.W is a hydrogen, C
1-10Alkyl or X, even more preferably hydrogen or C
1-4Alkyl.
Preferably, a value is approximately 1 or greater than 1, and more preferably 2 or greater than 2.Preferred a is about 6 or less than 6, and most preferred is about 4 or less than 4.Preferred b value is to be approximately 1.Preferred a and b sum are 2 or about 2 integers, preferredly are approximately 3 or greater than 3.Preferred a and b sum are approximately 6 or less than 6, preferredly are approximately 4 or less than 4.Preferred d is an integer between 1 and 4, more preferably between 2 and 4, be more preferably between 2 and 3.
The amine that preferably has molecular formula 2 is dimethylaminopropylamine, methoxy propanamine, dimethylaminoethylam,ne, dimethylaminobutylam,ne, methoxybutyl amine, methoxyethyl amine, ethoxy propylamine, propoxypropylamine, amine end-blocking polyalkylene ether (for example trimethylolpropane-three (polypropylene glycol, amine end-blocking) ether), aminopropyl morpholine, IPD and aminopropyl propane diamine.
In another embodiment, amine can be the aliphatics heterocycle that has a nitrogen-atoms on the heterocycle at least.Also can contain one or more nitrogen-atoms in this heterocyclic compound, oxygen atom, sulphur atom or two key.In addition, this heterocycle can comprise a plurality of rings, wherein contains nitrogen at least one ring.Preferred this compounds comprises morpholine, piperidines, pyrolidine, piperazine, 1,3,3 trimethyl 6-(azabicyclic) [3,2,1] octanes, thiazolidine, high piperazine (homopiperazine), aziridine, 1,4-(diazabicylo) [2,2,2] octane (DABCO), 1-amino-4-methyl piperazine and 3-pyrrolin.
In the another one embodiment, the amine that energy and organo-borane suitably cooperate is a kind of amidine, can be any cmpd that has the amidine structure, and for cooperating with organo-borane, this amidine must have enough bond energys.Suitable amidine comprises 1,8-(diazabicylo) [5,4] 11 carbon-7-alkene; Tetrahydropyrimidine; 2-methyl-2-imidazoline; With 1,1,3, the 3-TMG.
In a further embodiment, the amine that energy and organo-borane suitably cooperate is conjugated imines, can be all cpds that has the conjugated imines structure, as described in patent PCT/US00/33806, for cooperating with organo-borane, imines must have enough bond energys.This conjugated imines can be a straight chain, side chain imines or epimino.Preferred conjugated imines is the 4-dimethylamino naphthyridine; 2, two (dimethylamino) ring-propyleneimines of 3-; 3-(dimethyl amine) acrolein imines; 3-(dimethylamino) methacrolein imines (3-(dimethylamino) methacrole-inimine).
The mol ratio of preferred amines and organoborane compounds is 1.0: 1.0-3.0: 1.0.When mol ratio is lower than 1.0: 1.0, polymerization, aspects such as complexes stability and viscosity have problem.Can't bring more advantages though mol ratio is higher than 3.0: 1.0, but still can adopt.And amine too much can produce negative influence to the stability of adhesives or polymeric blends.More preferably the mol ratio of amines and organoborane compounds is 1.0: 1.0-2.0: 1.0.
The technology that provides as patent PCT/US00/33806 is provided, is easy to prepare organo-borane/amine complex.
Preferably, polymerizable material comprises acrylate and/or methacrylate compound.Especially preferred acrylate and methacrylate compound, it comprises methyl methacrylate, butyl methacrylate, ethylhexyl methacrylate, isobornyl methacrylate, tetrahydrofurfuryl methacrylate and methyl acrylic acid cyclohexyl methyl esters.
The composition of polymerizable thing can further comprise an amount of cmpd (a kind of association medium of separating) that can react with amine, and the borine that is discharged can make polymerization reaction take place.Required amine reaction compounds is in room temperature or is lower than room temperature, preferably is easy to the material of reaction of formation product at ambient temperature, and a kind of compound of using and solidifying of being easy under environmental conditions is provided then.Usually this compounds comprises acid, aldehyde, isocyanates, acid chloride, sulphonyl chlorides, their compound etc.Preferred amine reaction mixture is acid, especially bronsted acid and lewis acid and patent USP5, the cmpd described in 718,977, more preferably acrylic acid and methyl acrylic acid.
In polymerisable composition, suitable polymeric component massfraction accounts for 20% at least, preferably accounts for 30% at least, preferredly accounts for 40% at least.Individually,, suitable polymerizable components massfraction is no more than 95%, preferably is no more than 90%, especially preferredly is no more than 85%.
Suitable organo-borane/amine complex massfraction accounts for 0.2% at least, preferably accounts for 1% at least, preferredly accounts for 2% at least.In addition, suitable complex massfraction should be no more than 8%, preferably is no more than 6%, and is better as if being no more than 4%.
Exist if separate associating compound, its suitable massfraction accounts for 1% at least, preferably accounts for 1.5% at least, and is best as if accounting for 2% at least.Individually, the suitable associating compound massfraction of separating is no more than 8%, preferably is no more than 6%, especially preferredly is no more than 4%.
Detection through ASTM D1002 system shows: adhesives provided by the present invention can be bonded together the polypropylene member and the strenthening member of having filled 30% glass securely, and need not any component surface is carried out pretreatment.In addition, this adhesives also can use under thermal cycle and high humidity.Suitable thermal cycling temperature is-more than the 40-120 ℃.Humidity can be changed to fully saturated from drying.
The use of this adhesives can be adopted the mode of mentioning among the patent PCT/US00/33806.In addition, can also in compound, add other additive.Provided suitable additive among the patent PCT/US00/33806.
Suitable assembling can stand 100-120 ℃, even the thermal radiation of higher temperature.In addition, this assembling can also be born the weight that is applied in the middle of production process and the use, for example: and clash into bonnet with sudden force, on the bonnet handle, place weight, and the vibrations in the road traveling process and aging.In the middle of the practical application, select adhesive consumption and position according to the design and the structure of self-propelled vehicle.
In case on seat back system 20, used adhesives 66 and reinforcing member 32, then must reserve time enough solidifies (for example partly solidified, integrally curing, solidify air curing, heatcure as required, moisture-curable, chemosetting, photocuring etc.) adhesives 66, be connected on the base plate 26 to guarantee reinforcing member 32.Adhesives is preferably in room temperature (general 20-30 ℃) and solidifies down, also can solidify under higher or lower temperature conditions, to accelerate or the cure time that slows down.For guaranteeing that reinforcing member 32 is connected on the seat back system 20, can in solidification process, use fastener (for example high top drawing pin, clip etc.).In the middle of the use of seat back system 20, these fasteners can be detouchables, and can assist reinforcing member 32 to be connected thereto.
In general, wish this adhesives can show the appropriateness curing after ductility.The ductility of preferred adhesive, with the ductility of reinforcing member 32 materials, or constitute seat back system 20 or base plate 22 material ductility, lower equally high among the two ductility values.Yet the ductility of preferred adhesives, with the ductility of reinforcing member 32 materials, or constitute seat back system 20 or base plate 22 material ductility, higher equally high among the two ductility values.
Favourable result shows: make the back of seat that has the strenthening member that is made of another kind of material, can reach low fabrication cycle according to the present invention.For example, the fabrication cycle of this seat back system can be no more than one minute, preferably is no more than for 40 seconds, preferredly is no more than for 30 seconds, and what be more preferably was no more than for 20 seconds.
In Fig. 1-2 B illustrated embodiment, reinforcing member 32 is connected to the back side (that is: passenger's reverse side on the back of seat) of seat back system 20.In addition, member as shown in the figure can also be set on the seat back system or a plurality of positions of its in-to-in.One or more strenthening members can be arranged on the back side of seat back panel, one or morely can be arranged on the front, or are integrated in the inside of seat back panel.One or more strenthening members can also be along the exterior boundary setting of seat back panel.Also can consider these strenthening members horizontal along seat back panel, vertically, level, vertical, tilt or their array configuration setting.
In this embodiment, reinforcing member 32 is connected in the integrated strenthening member of seat back system 20.And reinforcing member 32 also can be arranged in the space (for example die cavity or through hole) or the plane on.
According to the present invention, seat back panel all can comprise one or more projections in the strenthening member, to assist the strenthening member setting and to be connected on the seat back panel.Preferably, projection can be inserted in the corresponding space (for example die cavity or through hole), and it can be a reinforcing member, the form that seat back panel or both have concurrently.Shown in Figure 3 is a plurality of projections 70 of stretching out from timber 60, and these projections 70 can be inserted the through hole 72 on the reinforcing member 32.
During concrete the application, should be according to following some or all criterions, the design of each strenthening member of optimization and position, or its making pattern in back of seat.For each application, can enjoy with those skilled in the art: use this concrete strenthening member can help to reduce because self-propelled vehicle is fast quickens or slow down soon or bending effect that seat rear passenger or goods (for example roof-mounted center safety strap, the pinnacle of roof-mounted child safety seat and luggage) are caused.For example, one preferred embodiment in, ruggedized construction of selecting for use usually or pattern are that the strenthening member that will have higher bending moment vertically is set to coilable curved ramp place.
Seat back system provided by the invention may be used on front stall, back seat, and folded seat etc. are located.Also can consider to be processed into and be applicable to the child safety seat tether, the seat back system of postmedian safety strap.This system also should meet the standard (for example strength criterion) that pre-establishes.Patent USP60/414, in 040 to seat, tether, safety strap and standard have been carried out detailed discussion.
Though the present invention has only related to automotive vehicle seat system, skilled worker skilled worker will recognize that this system also can be applicable to other seat, as aircraft and bus seat or auditorium and stadium seat.
Below only be to exemplified embodiment of the present invention.And those skilled in the art are by above said content, and accompanying drawing and claim can recognize, and are such just as defined by the following claims, under the prerequisite that does not depart from character of the present invention and scope, can carry out various changes, improve and distortion.Especially for described compound, assembling is installed, and the various functions that component etc. show under the situation of no certain illustrated, are not equal to term institute description scheme even if having the item of specific function, adopt this term description corresponding entry yet.In addition, the concrete feature that relates in embodiment can combine with the feature in other illustrated embodiment.
Claims (20)
1. motor vehicle seat chair back system method for making comprises:
Provide one at least at first base plate of self-propelled vehicle part lateral extent, this first base plate is limited and is provided with the main wall of crossing over continuously basically between whole peripheral boundary by peripheral boundary;
Provide one to be arranged at reinforcing member on this first base plate, wherein:
I) this first base plate is made by plastic material, has a match surface on it at least;
Ii) reinforcing member is made by the another kind of material that is different from the first base plate plastic material, has a match surface on it at least; And
Adopt a kind of adhesives that the match surface of the match surface of reinforcing member and first base plate is bonding, thus, reinforcing member substantial lateral ground, end wise or two to stretching along main wall with having concurrently.
2. method according to claim 1, wherein, at least one match surface of described reinforcing member or at least one match surface of described first base plate are low-yield surfaces, and adhesives can be bonded on the low-yield surface.
3. method according to claim 2, wherein, the surface energy on the low-yield surface of being made by plastic material is lower than 45mJ/m
2
4. method according to claim 1 and 2, wherein, described plastic material comprises a kind of poly-mer, this poly-mer is selected from polyolefin, polystyrene, polyamide, polybutylene terephthalate, acrylonitrile-butadiene-styrene, polycarbonate or their combination.
5. method according to claim 4, wherein, plastic material comprises a kind of filler.
6. method according to claim 5, wherein, filler is selected from short glass fiber, long glass fibres, short natural fiber or the right fiber of the vast of heaven.
7. according to the described method of claim 1,2 or 3, wherein, described plastic material is selected from the polypropylene of having filled short glass fiber, has filled the polypropylene of long glass fibres, has filled the polyamide and the polyamide alloy of having filled glass of glass.
8. according to any described method among the claim 1-3,5,6, wherein, reinforcing member and match surface thereof are made of metal, and described metal is selected from steel, aluminium or their combination.
9. according to any described method among the claim 1-3,5,6, it further comprises, adhesives is applied directly on the match surface of base plate, and described base plate match surface is not carried out pretreatment.
10. according to any described method among the claim 1-3,5,6, wherein, adhesives comprises: a kind of organo-borane/amine complex and can be by the free radical polymerization polymerization have undersaturated one or more monomers of ethylene linkage, oligomer or a poly-mer.
11. method according to claim 10, wherein, adhesives further comprises a kind of cmpd, and this cmpd can cause complex to separate to discharge organo-borane, has the polymerization of undersaturated one or more monomers of ethylene linkage, oligomer or poly-mer with initiation.
12. method according to claim 10, wherein, the amine moiety in organo-borane/amine complex is selected from: the amine with amidine structural constituent; The aliphatics heterocycle that in heterocycle, has at least one nitrogen; Additional have one or more hydrogen bonds to accept the primary amine of group, wherein accepts to have at least two carbon atoms between the group at primary amine and hydrogen bond; Or conjugated imines.
13. method according to claim 10, wherein, amine is selected from: dimethylaminopropylamine, methoxy propanamine, dimethylaminoethylam,ne, dimethylaminobutylam,ne, methoxybutyl amine, methoxyethyl amine, ethoxy propylamine, propoxypropylamine, the polyalkylene ether of amine end-blocking, aminopropyl morpholine, IPD and aminopropyl propane diamine.
14. method according to claim 13, wherein, amine end-blocking polyalkylene ether is trimethylolpropane-three (polypropylene glycol-amine end-blocking) ether.
15. method according to claim 10, wherein, the organo-borane in organic boron/amine complex partly is selected from trialkylborane or alkyl-cycloalkyl borine.
16. according to any described method among claim 1-3,5,6, the 11-15, wherein, one or more profile phases that at least one match surface limited on one or more profiles that at least one match surface limited on the reinforcing member and the base plate are corresponding.
17. method according to claim 16, wherein, described one or more profiles of reinforcing member are limited by timber or groove at least in part, and described one or more profiles of base plate are limited by timber or groove at least in part.
18. according to any described method among claim 1-3,5,6, the 11-15,17, wherein, the method for making of base plate is selected from compression molding, injection moulding or blow moulding.
19. according to any described method among claim 1-3,5,6, the 11-15,17, wherein, the fabrication cycle of seat back system was no more than for 40 seconds.
20. according to any described method among claim 1-3,5,6, the 11-15,17, wherein, the fabrication cycle of seat back system was no more than for 30 seconds.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US44711803P | 2003-02-13 | 2003-02-13 | |
| US60/447,118 | 2003-02-13 | ||
| US10/755,897 | 2004-01-13 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1747854A CN1747854A (en) | 2006-03-15 |
| CN100427336C true CN100427336C (en) | 2008-10-22 |
Family
ID=36166948
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2004800037655A Expired - Fee Related CN100427336C (en) | 2003-02-13 | 2004-02-10 | Seating system and method of forming same |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100427336C (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9217066B2 (en) * | 2008-03-31 | 2015-12-22 | Ford Global Technologies, Llc | Structural polymer insert and method of making the same |
| CN104494472A (en) * | 2014-05-28 | 2015-04-08 | 苏州雷姆斯汽车工程有限公司 | Carbon fiber reinforced safety seat base |
| CN107249933B (en) * | 2015-02-06 | 2020-03-17 | 安道拓卢森堡控股有限公司 | Method for connecting vehicle seat parts and vehicle seat |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1192756A (en) * | 1995-08-11 | 1998-09-09 | 美国3M公司 | Organoborane polyamine complex initiator system and polymerizable compositions made therewith |
| CN1218752A (en) * | 1997-12-03 | 1999-06-09 | 本田技研工业株式会社 | Chassis frame for motorcycle etc. |
| CN1291950A (en) * | 1998-03-03 | 2001-04-18 | 丹麦泡沫材料有限公司 | Seat, especially for vehicle |
| US20020058764A1 (en) * | 1999-12-17 | 2002-05-16 | Sonnenschein Mark F. | Amine organoborane complex polymerization initiators and polymerizable compositions |
| US9461346B2 (en) * | 2010-10-12 | 2016-10-04 | GM Global Technology Operations LLC | Method for air cooling of an electric vehicle traction battery with flow shifting |
-
2004
- 2004-02-10 CN CNB2004800037655A patent/CN100427336C/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1192756A (en) * | 1995-08-11 | 1998-09-09 | 美国3M公司 | Organoborane polyamine complex initiator system and polymerizable compositions made therewith |
| CN1218752A (en) * | 1997-12-03 | 1999-06-09 | 本田技研工业株式会社 | Chassis frame for motorcycle etc. |
| CN1291950A (en) * | 1998-03-03 | 2001-04-18 | 丹麦泡沫材料有限公司 | Seat, especially for vehicle |
| US20020058764A1 (en) * | 1999-12-17 | 2002-05-16 | Sonnenschein Mark F. | Amine organoborane complex polymerization initiators and polymerizable compositions |
| US9461346B2 (en) * | 2010-10-12 | 2016-10-04 | GM Global Technology Operations LLC | Method for air cooling of an electric vehicle traction battery with flow shifting |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1747854A (en) | 2006-03-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100341738C (en) | Automobile assembly | |
| CN100410126C (en) | Improved instrument panel assembly and method of forming same | |
| CA2513118A1 (en) | Seating system and method of forming same | |
| CN100457499C (en) | Improved seating system | |
| JP2010168040A5 (en) | ||
| CN102574549B (en) | Motor vehicles front end | |
| JP2008507430A (en) | Multilayer film, sheet and method for producing article derived therefrom | |
| CN101128308A (en) | Bonded hybrid structure | |
| US7926870B2 (en) | Modular assembly for a vehicle | |
| CN102036851A (en) | Improved vehicular seating system | |
| CN100427336C (en) | Seating system and method of forming same | |
| CN1791520A (en) | Instrument panel assembly and method of forming same | |
| CN1871108A (en) | Multi-assembly injection moulding of decorative panel | |
| EP3103840B1 (en) | Polymeric resin composition for steering wheel remote controller bezel | |
| WO2004108483A2 (en) | Air bag system and method of forming the same | |
| US8015635B1 (en) | Structural bunk system | |
| JP2008024173A (en) | Interior trim part for automobile and its manufacturing method | |
| OOMURA et al. | Development of Novel Polypropylene Foaming/Molding Technologies and Products for Sumiceller® | |
| Vogelei | Corvette Plastic Progress Enters Third Decade | |
| JP2006096304A (en) | Interior part for car |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| ASS | Succession or assignment of patent right |
Owner name: STYRON EUROPE GMBH Free format text: FORMER OWNER: STYRON GMBH Effective date: 20111121 Owner name: STYRON GMBH Free format text: FORMER OWNER: THE DOW GLOBAL TECHNOLOGIES INC. Effective date: 20111121 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20111121 Address after: Horgen Switzerland Patentee after: STYRON EUROPE GmbH Address before: Michigan Patentee before: Scarlett Dillon Co.,Ltd. Effective date of registration: 20111121 Address after: Michigan Patentee after: Scarlett Dillon Co.,Ltd. Address before: michigan Patentee before: Dow Global Technologies Inc. |
|
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20081022 Termination date: 20120210 |