JPH10180878A - Method of manufacturing vibration welded molded product made of polyamide resin - Google Patents
Method of manufacturing vibration welded molded product made of polyamide resinInfo
- Publication number
- JPH10180878A JPH10180878A JP8343872A JP34387296A JPH10180878A JP H10180878 A JPH10180878 A JP H10180878A JP 8343872 A JP8343872 A JP 8343872A JP 34387296 A JP34387296 A JP 34387296A JP H10180878 A JPH10180878 A JP H10180878A
- Authority
- JP
- Japan
- Prior art keywords
- polyamide resin
- vibration
- molded product
- welding
- welded
- 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.)
- Pending
Links
- 229920006122 polyamide resin Polymers 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 12
- 238000003466 welding Methods 0.000 claims abstract description 47
- 238000002844 melting Methods 0.000 claims abstract description 10
- 230000008018 melting Effects 0.000 claims abstract description 10
- 239000003365 glass fiber Substances 0.000 claims description 17
- 239000004677 Nylon Substances 0.000 claims description 15
- 229920001778 nylon Polymers 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 13
- 238000000465 moulding Methods 0.000 claims description 9
- 239000002253 acid Substances 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- 238000001746 injection moulding Methods 0.000 description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- 230000001771 impaired effect Effects 0.000 description 3
- 150000003951 lactams Chemical class 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- PBLZLIFKVPJDCO-UHFFFAOYSA-N 12-aminododecanoic acid Chemical compound NCCCCCCCCCCCC(O)=O PBLZLIFKVPJDCO-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920006351 engineering plastic Polymers 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- LWBHHRRTOZQPDM-UHFFFAOYSA-N undecanedioic acid Chemical compound OC(=O)CCCCCCCCCC(O)=O LWBHHRRTOZQPDM-UHFFFAOYSA-N 0.000 description 2
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- XDOLZJYETYVRKV-UHFFFAOYSA-N 7-Aminoheptanoic acid Chemical compound NCCCCCCC(O)=O XDOLZJYETYVRKV-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000005749 Copper compound Substances 0.000 description 1
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 1
- JJOJFIHJIRWASH-UHFFFAOYSA-N Eicosanedioic acid Natural products OC(=O)CCCCCCCCCCCCCCCCCCC(O)=O JJOJFIHJIRWASH-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 239000004957 Zytel Substances 0.000 description 1
- 229920006102 Zytel® Polymers 0.000 description 1
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- CJYXCQLOZNIMFP-UHFFFAOYSA-N azocan-2-one Chemical compound O=C1CCCCCCN1 CJYXCQLOZNIMFP-UHFFFAOYSA-N 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- -1 for example Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- KLNPWTHGTVSSEU-UHFFFAOYSA-N undecane-1,11-diamine Chemical compound NCCCCCCCCCCCN KLNPWTHGTVSSEU-UHFFFAOYSA-N 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/71—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/02—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
- B29C65/06—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using friction, e.g. spin welding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/50—General aspects of joining tubular articles; General aspects of joining long products, i.e. bars or profiled elements; General aspects of joining single elements to tubular articles, hollow articles or bars; General aspects of joining several hollow-preforms to form hollow or tubular articles
- B29C66/51—Joining tubular articles, profiled elements or bars; Joining single elements to tubular articles, hollow articles or bars; Joining several hollow-preforms to form hollow or tubular articles
- B29C66/54—Joining several hollow-preforms, e.g. half-shells, to form hollow articles, e.g. for making balls, containers; Joining several hollow-preforms, e.g. half-cylinders, to form tubular articles
- B29C66/547—Joining several hollow-preforms, e.g. half-cylinders, to form tubular articles, e.g. endless tubes
- B29C66/5474—Joining several hollow-preforms, e.g. half-cylinders, to form tubular articles, e.g. endless tubes for making fork-shaped pieces, i.e. with 3 branches, e.g. Y-shaped pieces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/90—Measuring or controlling the joining process
- B29C66/91—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux
- B29C66/914—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux
- B29C66/9141—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux by controlling or regulating the temperature
- B29C66/91411—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux by controlling or regulating the temperature of the parts to be joined, e.g. the joining process taking the temperature of the parts to be joined into account
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/90—Measuring or controlling the joining process
- B29C66/91—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux
- B29C66/919—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/90—Measuring or controlling the joining process
- B29C66/91—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux
- B29C66/919—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges
- B29C66/9192—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges in explicit relation to another variable, e.g. temperature diagrams
- B29C66/91921—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges in explicit relation to another variable, e.g. temperature diagrams in explicit relation to another temperature, e.g. to the softening temperature or softening point, to the thermal degradation temperature or to the ambient temperature
- B29C66/91931—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges in explicit relation to another variable, e.g. temperature diagrams in explicit relation to another temperature, e.g. to the softening temperature or softening point, to the thermal degradation temperature or to the ambient temperature in explicit relation to the fusion temperature or melting point of the material of one of the parts to be joined
- B29C66/91935—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges in explicit relation to another variable, e.g. temperature diagrams in explicit relation to another temperature, e.g. to the softening temperature or softening point, to the thermal degradation temperature or to the ambient temperature in explicit relation to the fusion temperature or melting point of the material of one of the parts to be joined lower than said fusion temperature
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/01—General aspects dealing with the joint area or with the area to be joined
- B29C66/05—Particular design of joint configurations
- B29C66/10—Particular design of joint configurations particular design of the joint cross-sections
- B29C66/11—Joint cross-sections comprising a single joint-segment, i.e. one of the parts to be joined comprising a single joint-segment in the joint cross-section
- B29C66/114—Single butt joints
- B29C66/1142—Single butt to butt joints
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/90—Measuring or controlling the joining process
- B29C66/91—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux
- B29C66/912—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by measuring the temperature, the heat or the thermal flux
- B29C66/9121—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by measuring the temperature, the heat or the thermal flux by measuring the temperature
- B29C66/91211—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by measuring the temperature, the heat or the thermal flux by measuring the temperature with special temperature measurement means or methods
- B29C66/91216—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by measuring the temperature, the heat or the thermal flux by measuring the temperature with special temperature measurement means or methods enabling contactless temperature measurements, e.g. using a pyrometer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/90—Measuring or controlling the joining process
- B29C66/91—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux
- B29C66/912—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by measuring the temperature, the heat or the thermal flux
- B29C66/9121—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by measuring the temperature, the heat or the thermal flux by measuring the temperature
- B29C66/91221—Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by measuring the temperature, the heat or the thermal flux by measuring the temperature of the parts to be joined
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/90—Measuring or controlling the joining process
- B29C66/92—Measuring or controlling the joining process by measuring or controlling the pressure, the force, the mechanical power or the displacement of the joining tools
- B29C66/929—Measuring or controlling the joining process by measuring or controlling the pressure, the force, the mechanical power or the displacement of the joining tools characterized by specific pressure, force, mechanical power or displacement values or ranges
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/90—Measuring or controlling the joining process
- B29C66/95—Measuring or controlling the joining process by measuring or controlling specific variables not covered by groups B29C66/91 - B29C66/94
- B29C66/951—Measuring or controlling the joining process by measuring or controlling specific variables not covered by groups B29C66/91 - B29C66/94 by measuring or controlling the vibration frequency and/or the vibration amplitude of vibrating joining tools, e.g. of ultrasonic welding tools
- B29C66/9513—Measuring or controlling the joining process by measuring or controlling specific variables not covered by groups B29C66/91 - B29C66/94 by measuring or controlling the vibration frequency and/or the vibration amplitude of vibrating joining tools, e.g. of ultrasonic welding tools characterised by specific vibration frequency values or ranges
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/90—Measuring or controlling the joining process
- B29C66/95—Measuring or controlling the joining process by measuring or controlling specific variables not covered by groups B29C66/91 - B29C66/94
- B29C66/951—Measuring or controlling the joining process by measuring or controlling specific variables not covered by groups B29C66/91 - B29C66/94 by measuring or controlling the vibration frequency and/or the vibration amplitude of vibrating joining tools, e.g. of ultrasonic welding tools
- B29C66/9517—Measuring or controlling the joining process by measuring or controlling specific variables not covered by groups B29C66/91 - B29C66/94 by measuring or controlling the vibration frequency and/or the vibration amplitude of vibrating joining tools, e.g. of ultrasonic welding tools characterised by specific vibration amplitude values or ranges
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- High Energy & Nuclear Physics (AREA)
- Plasma & Fusion (AREA)
- Reinforced Plastic Materials (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】
【課題】 溶着強度の大きいポリアミド樹脂製振動溶着
成形品を製造する方法を提供する。
【解決手段】ポリアミド樹脂を用いて一次成形した複数
の成形品の振動溶着時の温度を50℃以上、該ポリアミ
ド樹脂の融点未満にすることを特徴とするポリアミド樹
脂製振動溶着成形品の製造方法。(57) [Problem] To provide a method for producing a vibration-welded molded product made of polyamide resin having high welding strength. A method for producing a vibration-welded molded article made of a polyamide resin, wherein a temperature at the time of vibration welding of a plurality of molded articles primarily formed using a polyamide resin is set to 50 ° C. or higher and lower than a melting point of the polyamide resin. .
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ポリアミド樹脂製
振動溶着成形品の製造方法に関するものであり、詳しく
は、一次成形した複数の成形品を振動溶着法により一体
化したポリアミド樹脂製振動溶着成形品の製造方法に関
するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a vibration-welded molded article made of a polyamide resin, and more particularly, to a vibration-welded molding of a polyamide resin in which a plurality of primary molded articles are integrated by a vibration welding method. The present invention relates to a method for manufacturing a product.
【0002】[0002]
【従来の技術】近年、プラスチックの用途が拡大され、
その特性を生かし、各種工業製品、例えば自動車エンジ
ンのインテークマニホールドなども振動溶着法により樹
脂化が試みられている。樹脂化の材料としてはガラス繊
維強化66ナイロンまたはガラス繊維強化6ナイロンな
どが用いられている。しかし、従来の製造方法では、一
次成形された成形品を振動溶着法により溶着しても充分
に満足できる溶着強度が得られず、例えば振動溶着成形
品が中空体成形品である自動車エンジンのインテークマ
ニホールドの場合においては十分な耐圧強度が得られ
ず、エンジンのバックファイアなどによって内圧が増大
したときに破裂に結びつく危険性があるため、溶着面積
の増大等の設計変更を余儀なくされることが多かった。2. Description of the Related Art In recent years, applications of plastics have been expanded,
Taking advantage of this property, various industrial products, such as intake manifolds for automobile engines, have been converted into resins by the vibration welding method. As a material for resinification, glass fiber reinforced 66 nylon or glass fiber reinforced 6 nylon is used. However, according to the conventional manufacturing method, even if the primary molded article is welded by the vibration welding method, a sufficiently satisfactory welding strength cannot be obtained. For example, an intake of an automobile engine in which the vibration welded molded article is a hollow body molded article. In the case of a manifold, sufficient pressure resistance cannot be obtained, and when the internal pressure increases due to an engine backfire or the like, there is a risk of rupture.Therefore, design changes such as an increase in welding area are often required. Was.
【0003】[0003]
【発明が解決しようとする課題】本発明の目的は、溶着
強度の大きいポリアミド樹脂製振動溶着成形品を製造す
る方法を提供することにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a method for producing a vibration-welded molded article made of a polyamide resin having a high welding strength.
【0004】[0004]
【課題を解決するための手段】本発明は、上述の問題を
解決するためになされたものであり、その要旨は、ポリ
アミド樹脂を用いて一次成形した複数の成形品の振動溶
着時の温度を50℃以上、該ポリアミド樹脂の融点未満
にすることを特徴とするポリアミド樹脂製振動溶着成形
品の製造方法に存する。SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned problems, and the gist of the present invention is to determine the temperature at the time of vibration welding of a plurality of molded products which are primarily molded using a polyamide resin. The present invention provides a method for producing a vibration-welded molded article made of a polyamide resin, wherein the temperature is 50 ° C. or higher and lower than the melting point of the polyamide resin.
【0005】以下、本発明につき詳細に説明する。本発
明におけるポリアミド樹脂としては、重合可能なω−ア
ミノ酸類もしくはそのラクタム類、好ましくは3員環以
上のラクタム、または二塩基酸類とジアミン類などを原
料とし、これらの重縮合によって得られるポリアミド樹
脂である。具体的には、原料のω−アミノ酸類として
は、ε−アミノカプロン酸、7−アミノヘプタン酸、9
−アミノノナン酸、11−アミノウンデカン酸、12−
アミノドデカン酸が挙げられる。ラクタム類としては、
ε−カプロラクタム、エナントラクタム、カプリルラク
タム、ラウリルラクタム、α−ピロリドン、α−ピペリ
ドンが挙げられる。Hereinafter, the present invention will be described in detail. As the polyamide resin in the present invention, a polymerizable ω-amino acid or a lactam thereof, preferably a lactam having three or more ring members, or a polyamide resin obtained by polycondensation of a dibasic acid and a diamine as a raw material It is. Specifically, ω-amino acids as raw materials include ε-aminocaproic acid, 7-aminoheptanoic acid,
-Aminononanoic acid, 11-aminoundecanoic acid, 12-
Aminododecanoic acid; As lactams,
ε-caprolactam, enantholactam, caprylactam, lauryl lactam, α-pyrrolidone, α-piperidone.
【0006】二塩基酸類としては、アジピン酸、グルタ
ル酸、ピメリン酸、スベリン酸、アゼライン酸、セバシ
ン酸、ウンデカンジオン酸、ドデカジオン酸、ヘキサデ
カジオン酸、ヘキサデセンジオン酸、エイコサンジオン
酸、エイコサジエンジオン酸、ジグリコール酸、2,
2,4−トリメチルアジピン酸、キシリレンジカルボン
酸、1,4−シクロヘキサンジカルボン酸、テレフタル
酸、イソフタル酸が挙げられる。Examples of the dibasic acids include adipic acid, glutaric acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, undecandioic acid, dodecadionic acid, hexadecadionic acid, hexadecenedionic acid, eicosandioic acid, and eicosadi. Endionic acid, diglycolic acid, 2,
Examples include 2,4-trimethyladipic acid, xylylenedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, terephthalic acid, and isophthalic acid.
【0007】ジアミン類としては、ヘキサメチレンジア
ミン、テトラメチレンジアミン、ノナメチレンジアミ
ン、ウンデカメチレンジアミン、ドデカメチレンジアミ
ン、2,2,4(または2,4,4)−トリメチルヘキ
サメチレンジアミン、ビス−(4,4’−アミノシクロ
ヘキシル)メタン、メタキシリレンジアミンが挙げられ
る。[0007] Diamines include hexamethylenediamine, tetramethylenediamine, nonamethylenediamine, undecamethylenediamine, dodecamethylenediamine, 2,2,4 (or 2,4,4) -trimethylhexamethylenediamine, bis-methylenediamine and bis-methylenediamine. (4,4'-aminocyclohexyl) methane and meta-xylylenediamine.
【0008】本発明で使用されるポリアミド樹脂として
は、好ましくは、6ナイロン、66ナイロンおよび66
/6共重合ナイロンが挙げられる。また、上記のポリア
ミド樹脂の複数種を使用することもできる。[0008] The polyamide resin used in the present invention is preferably 6 nylon, 66 nylon or 66 nylon.
/ 6 copolymerized nylon. Further, a plurality of the above-mentioned polyamide resins may be used.
【0009】本発明におけるポリアミド樹脂は、適度な
範囲内の重合度、すなわち一定範囲内の相対粘度を有す
るものが好ましい。ポリアミド樹脂の相対粘度は、JI
SのK6810に従って98%硫酸中濃度1%、温度2
5℃で測定した値で、好ましくは2.0〜4.0であ
り、より好ましくは2.5〜3.7である。相対粘度が
低いと、溶着強度が小さくなり、逆に高すぎると、流動
性を損ない表面平滑性不良となりやすい。The polyamide resin in the present invention preferably has a degree of polymerization within an appropriate range, that is, a resin having a relative viscosity within a certain range. The relative viscosity of the polyamide resin is determined by JI
S 1% concentration in 98% sulfuric acid according to K6810 of S, temperature 2
The value measured at 5 ° C. is preferably 2.0 to 4.0, more preferably 2.5 to 3.7. If the relative viscosity is low, the welding strength will be low, and if it is too high, the fluidity will be impaired and the surface smoothness will be poor.
【0010】本発明において、ポリアミド樹脂がガラス
繊維強化ポリアミド樹脂である場合に使用されるガラス
繊維としては、熱可塑性樹脂において通常使用されるも
のでよく、Eガラス(無アルカリガラス)から作られる
チョップドストランドが好ましい。ガラス繊維の繊維径
は、好ましくは1〜20μmであり、より好ましくは5
〜15μmである。ガラス繊維はポリアミドとの接着向
上のためシランカップリング剤などで表面処理されてい
ることが好ましい。ガラス繊維の配合量は、好ましくは
ガラス繊維強化ポリアミド樹脂の10〜60重量%であ
り、より好ましくは20〜50重量%であり、さらに好
ましくは30〜40重量%である。配合量が少なすぎる
と溶着強度が低下し、多すぎると表面平滑性が損なわれ
やすい。In the present invention, the glass fibers used when the polyamide resin is a glass fiber reinforced polyamide resin may be those usually used in thermoplastic resins, and may be chopped made of E glass (alkali-free glass). Strands are preferred. The fiber diameter of the glass fiber is preferably 1 to 20 μm, more preferably 5 μm.
1515 μm. The glass fiber is preferably surface-treated with a silane coupling agent or the like to improve the adhesion to the polyamide. The compounding amount of the glass fiber is preferably 10 to 60% by weight of the glass fiber reinforced polyamide resin, more preferably 20 to 50% by weight, and further preferably 30 to 40% by weight. If the amount is too small, the welding strength is reduced, and if it is too large, the surface smoothness tends to be impaired.
【0011】本発明におけるポリアミド樹脂中には、本
発明の効果を損なわない範囲において、ガラス繊維以外
の無機充填材、例えばガラスフレーク、ガラスビーズ、
マイカ、タルク、カオリン、ウォラストナイト、チタン
酸カリウムウィスカー等を配合してもよい。また、銅化
合物などの熱安定剤、離型剤、カーボンブラックなどの
着色剤等の公知の添加剤を配合してもよい。これらの配
合は、樹脂の重合から成形までの任意の段階で実施する
ことができるが、押出機を用いて溶融混練するのが好ま
しい。In the polyamide resin of the present invention, inorganic fillers other than glass fibers, for example, glass flakes, glass beads, and the like, as long as the effects of the present invention are not impaired.
Mica, talc, kaolin, wollastonite, potassium titanate whiskers and the like may be blended. Further, known additives such as a heat stabilizer such as a copper compound, a releasing agent, and a coloring agent such as carbon black may be blended. These blending can be carried out at any stage from polymerization of the resin to molding, but it is preferable to carry out melt kneading using an extruder.
【0012】本発明においては、ポリアミド樹脂を用い
て、まず複数の部品をそれぞれ一次成形する。一次成形
により得られる成形品の成形法としては、熱可塑性樹脂
の成形において通常用いられる成形法が適用され、好ま
しくは射出成形法が挙げられる。本発明における一次成
形により得られる複数の成形品の形状としては、振動溶
着により溶着しうる接合面を有する形状であればよく、
複数の成形品はお互いに同じ形状であっても異なる形状
であってもよく、例えば、図1に示すような形状の成形
品や図4に示す中空体である三方管を長手方向に切断し
た形状の成形品などが挙げられる。In the present invention, first, a plurality of components are firstly molded using a polyamide resin. As a molding method of a molded article obtained by primary molding, a molding method generally used in molding of a thermoplastic resin is applied, and preferably, an injection molding method is used. The shape of the plurality of molded products obtained by the primary molding in the present invention may be any shape having a joining surface that can be welded by vibration welding,
The plurality of molded products may have the same shape or different shapes from each other. For example, a molded product having a shape as shown in FIG. 1 or a three-way tube which is a hollow body shown in FIG. 4 is cut in the longitudinal direction. Shaped molded articles are exemplified.
【0013】本発明の製造方法においては、一次成形し
た複数の成形品を振動溶着により溶着するに際し、一次
成形した成形品(一次成形品と称することもある。)の
振動溶着時の温度を50℃以上、一次成形品に用いたポ
リアミド樹脂の融点未満にして、一次成形品を溶着接合
し、目的とするポリアミド樹脂製振動溶着成形品を得
る。In the manufacturing method of the present invention, when a plurality of primary molded products are welded by vibration welding, the temperature of the primary molded product (sometimes referred to as a primary molded product) at the time of vibration welding is set to 50. The temperature is set to not less than 0 ° C. and lower than the melting point of the polyamide resin used for the primary molded product, and the primary molded product is welded and joined to obtain the desired vibration-welded molded product made of the polyamide resin.
【0014】一次成形品の振動溶着時の温度が低いと、
溶着強度の向上効果が小さく、一次成形品の振動溶着時
の温度がその融点を越えると、成形品が溶融してしまう
ので好ましくない。一次成形品の振動溶着時の温度は、
好ましくは、70℃以上、一次成形品に用いたポリアミ
ド樹脂の融点より10℃低い温度以下であり、より好ま
しくは、80℃以上、一次成形品に用いたポリアミド樹
脂の融点より20℃低い温度以下である。If the temperature during vibration welding of the primary molded product is low,
If the effect of improving the welding strength is small and the temperature at the time of vibration welding of the primary molded product exceeds its melting point, the molded product is undesirably melted. The temperature during vibration welding of primary molded products is
Preferably, the temperature is 70 ° C. or higher and 10 ° C. or lower than the melting point of the polyamide resin used for the primary molded product, and more preferably 80 ° C. or higher, and 20 ° C. or lower than the melting point of the polyamide resin used for the primary molded product. It is.
【0015】振動溶着の際の一次成形品の温度は、上記
の範囲内であれば、振動溶着を行う雰囲気の温度を上記
の温度範囲内にしてもよく、一次成形品をあらかじめ加
温し上記の温度範囲内にしてもよい。また、一次成形直
後、成形品の温度が上記の範囲内にあるうちに振動溶着
を行うこともできる。If the temperature of the primary molded product during vibration welding is within the above range, the temperature of the atmosphere in which the vibration welding is performed may be within the above temperature range. Temperature range. Immediately after the primary molding, vibration welding can be performed while the temperature of the molded product is within the above range.
【0016】振動溶着における振動の周波数は、好まし
くは100〜300Hzであり、振幅は、好ましくは
0.5〜2.0mmであり、より好ましくは0.8〜
1.6mmであり、溶着圧力は、好ましくは5〜100
kg/cm2である。所定の圧力下にあるべき溶着時間
は、目的とする溶け代が得られるように適宜設定し、振
動を停止した後の保持圧力および保持時間は、溶着部が
十分固化するように適宜設定する。The frequency of vibration in vibration welding is preferably 100 to 300 Hz, and the amplitude is preferably 0.5 to 2.0 mm, more preferably 0.8 to 2.0 mm.
1.6 mm, and the welding pressure is preferably 5 to 100
kg / cm 2 . The welding time that should be under a predetermined pressure is appropriately set so as to obtain a desired melting margin, and the holding pressure and the holding time after stopping the vibration are appropriately set so that the welded portion is sufficiently solidified.
【0017】以下、本発明を実施例により更に詳細に説
明するが、本発明はその要旨を超えない限り、以下の実
施例に限定されるものではない。Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited to the following examples unless it exceeds the gist.
【実施例】尚、以下の実施例および比較例において使用
したポリアミド樹脂は次のとおりである。The polyamide resins used in the following Examples and Comparative Examples are as follows.
【0018】(1)6ナイロン:三菱エンジニアリング
プラスチックス株式会社製NOVAMID1015J。
相対粘度3.0。 (2)66ナイロン:デュポン社製ザイテル101NC
10。相対粘度3.0。 (3)66/6共重合ナイロン:AH塩(アジピン酸と
ヘキサメチレンジアミンの塩)とε−カプロラクタムの
モル比が9:1で融点が245℃の共重合ナイロン。相
対粘度3.0。(1) 6 nylon: NOVAMID1015J manufactured by Mitsubishi Engineering-Plastics Corporation.
Relative viscosity 3.0. (2) 66 nylon: Zytel 101NC manufactured by DuPont
10. Relative viscosity 3.0. (3) 66/6 copolymerized nylon: a copolymerized nylon having a 9: 1 molar ratio of AH salt (salt of adipic acid and hexamethylenediamine) and ε-caprolactam and a melting point of 245 ° C. Relative viscosity 3.0.
【0019】振動溶着強度の評価方法は次のとおりであ
る。 (4)溶着強度の測定用試験片:後記実施例において説
明する条件で射出成形し、図−1に示す2つの同一形状
の一次成形品を得る。続いて、後記実施例において説明
する条件で振動溶着して、図−2に示す振動溶着成形品
を得た。 (5)溶着強度の測定法:この振動溶着成形品を、オリ
エンテック株式会社製テンシロンUTM−III−50
0型試験機を使用し、引張速度5mm/min、チャッ
ク間距離50mmの条件で引張り、溶着部における破断
強度を溶着強度とした。The method for evaluating the vibration welding strength is as follows. (4) Test piece for measuring welding strength: Injection molding is performed under the conditions described in the following examples to obtain two primary molded articles having the same shape as shown in FIG. Subsequently, vibration welding was performed under the conditions described in Examples described later to obtain a vibration welded molded product shown in FIG. (5) Measuring method of welding strength: This vibration-welded molded product is manufactured by Orientec Co., Ltd. using Tensilon UTM-III-50.
Using a 0-type testing machine, tension was applied under the conditions of a tensile speed of 5 mm / min and a distance between chucks of 50 mm, and the breaking strength at the welded portion was defined as the weld strength.
【0020】〔実施例1〕表−1に記載のポリアミド樹
脂に、ガラス繊維(日本電気硝子株式会社製、商品名T
283H)が35重量%となるように配合しガラス繊維
強化ポリアミド樹脂組成物を得た。配合には、2軸混練
機を用い、設定温度は280℃とした。[Example 1] Polyamide resin shown in Table 1 was added to glass fiber (trade name T, manufactured by NEC Corporation).
283H) to 35% by weight to obtain a glass fiber reinforced polyamide resin composition. For the compounding, a twin-screw kneader was used, and the set temperature was 280 ° C.
【0021】得られたガラス繊維強化ポリアミド樹脂組
成物を、日精樹脂工業株式会社製のFS160S型射出
成形機を用いて、設定温度260℃で、設定金型温度8
0℃で、図1に示す2つの同一形状の一次成形品を得
た。熱風乾燥オーブン内で温めた一対の一次成形品を、
振動溶着治具で固定し、振動溶着を行う直前に表面温度
計により、一次成形品の温度を測定した。測定結果を表
−1に示す。The obtained glass fiber reinforced polyamide resin composition was molded at a set temperature of 260 ° C. and a set mold temperature of 8 using an FS160S type injection molding machine manufactured by Nissei Plastics Industry Co., Ltd.
At 0 ° C., two primary molded articles of the same shape shown in FIG. 1 were obtained. A pair of primary molded products warmed in a hot air drying oven,
It was fixed with a vibration welding jig, and the temperature of the primary molded product was measured with a surface thermometer immediately before performing the vibration welding. Table 1 shows the measurement results.
【0022】この一次成形品の一対を、日本エマソン株
式会社製の振動溶着機(VIBRATION WELD
ER Model 2800)を使用して、周波数24
0Hz、溶着圧力15.5kg/cm2、振幅1.5m
m、溶け代1.5mm、保持圧力:振動停止後の加圧力
15.5kg/cm2、保持時間5.0secで溶着し
て、図2に示す振動溶着成形品を得た。溶け代をコント
ロールするのには日本エマソン株式会社製のCX132
型非接触WDC溶着寸法制御装置を使用した。得られた
振動溶着成形品の溶着強度の測定結果を表−1に示す。[0022] A pair of the primary molded products is used as a vibration welding machine (Vibration Weld) manufactured by Emerson Japan.
ER Model 2800) using frequency 24
0 Hz, welding pressure 15.5 kg / cm 2 , amplitude 1.5 m
m, welding margin 1.5 mm, holding pressure: welding pressure 15.5 kg / cm 2 after stopping vibration, holding time 5.0 sec, to obtain a vibration welded molded product shown in FIG. To control the melting allowance, CX132 manufactured by Emerson Japan
A mold non-contact WDC welding size control device was used. Table 1 shows the measurement results of the welding strength of the obtained vibration welding molded product.
【0023】〔実施例2〕一次成形品の温度を140℃
としたこと以外は実施例1と同様の条件で、振動溶着成
形品を得、溶着強度を測定した。測定結果を表−1に示
す。 〔実施例3〕 ポリアミド樹脂を
ガラス繊維強化66ナイロン(ガラス繊維含有量35重
量%)にし、射出成形の設定温度を280℃にし、一次
成形品の温度を140℃としたこと以外は実施例1と同
様の条件で、振動溶着成形品を得、溶着強度を測定し
た。測定結果を表−1に示す。Example 2 The temperature of the primary molded product was set to 140 ° C.
A vibration welded molded product was obtained under the same conditions as in Example 1, except that the welding strength was measured. Table 1 shows the measurement results. Example 3 Example 1 was repeated except that the polyamide resin was made of glass fiber reinforced 66 nylon (glass fiber content 35% by weight), the injection molding temperature was set at 280 ° C., and the temperature of the primary molded product was 140 ° C. Under the same conditions as described above, a vibration-welded molded product was obtained, and the welding strength was measured. Table 1 shows the measurement results.
【0024】〔実施例4〕ポリアミド樹脂をガラス繊維
強化66/6共重合ナイロン(ガラス繊維含有量35重
量%)にし、射出成形の設定温度を280℃にし、一次
成形品の温度を140℃としたこと以外は実施例1と同
様の条件で、振動溶着成形品を得、溶着強度を測定し
た。測定結果を表−1に示す。 〔比較例1〕一次成形品の温度を23℃としたこと以外
は実施例1と同様の条件で、振動溶着成形品を得、溶着
強度を測定した。測定結果を表−1に示す。Example 4 A polyamide resin was made of glass fiber reinforced 66/6 copolymerized nylon (glass fiber content: 35% by weight), the injection molding temperature was set to 280 ° C., and the temperature of the primary molded product was set to 140 ° C. Except for the above, a vibration-welded molded product was obtained under the same conditions as in Example 1, and the welding strength was measured. Table 1 shows the measurement results. Comparative Example 1 A vibration welded molded product was obtained under the same conditions as in Example 1 except that the temperature of the primary molded product was set to 23 ° C., and the welding strength was measured. Table 1 shows the measurement results.
【0025】〔比較例2〕一次成形品の温度を23℃と
したこと以外は実施例3と同様の条件で、振動溶着成形
品を得、溶着強度を測定した。測定結果を表−1に示
す。 〔比較例3〕 一次成形品の温度を23℃としたこと
以外は実施例4と同様の条件で、振動溶着成形品を得、
溶着強度を測定した。測定結果を表−1に示す。Comparative Example 2 A vibration-welded molded product was obtained under the same conditions as in Example 3 except that the temperature of the primary molded product was 23 ° C., and the welding strength was measured. Table 1 shows the measurement results. [Comparative Example 3] A vibration welded molded product was obtained under the same conditions as in Example 4 except that the temperature of the primary molded product was set to 23 ° C.
The welding strength was measured. Table 1 shows the measurement results.
【0026】[0026]
【表1】 [Table 1]
【0027】[0027]
【発明の効果】本発明の方法によって得られるポリアミ
ド樹脂製振動溶着成形品の溶着強度は著しく向上してお
り、各種分野への振動溶着成形品の適用が可能となり、
特に高い安全性を要求される自動車用インテークマニホ
ールドを製造する方法として有用である。The welding strength of the vibration-welded molded article made of a polyamide resin obtained by the method of the present invention is remarkably improved, and the vibration-welded molded article can be applied to various fields.
It is particularly useful as a method for manufacturing an intake manifold for an automobile that requires high safety.
【図1】一次成形品の形状(60mm×25mm×4m
m)の例を示す説明図FIG. 1 shows the shape of a primary molded product (60 mm × 25 mm × 4 m
Explanatory diagram showing an example of m)
【図2】振動溶着成形品の形状の例を示す説明図FIG. 2 is an explanatory view showing an example of the shape of a vibration welding molded product.
【図3】(a)、(b)は一対の中空体成形品の形状の
例を示す平面図FIGS. 3A and 3B are plan views showing examples of shapes of a pair of hollow body molded products.
【図4】振動溶着中空体成形品の例を示す概念図FIG. 4 is a conceptual diagram showing an example of a vibration-welded hollow body molded product.
1 溶着面 2、2’ 上部開口部 3 下部開口部 DESCRIPTION OF SYMBOLS 1 Welding surface 2, 2 'Upper opening 3 Lower opening
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI B29K 105:06 B29L 23:00 (72)発明者 人見 達也 神奈川県茅ヶ崎市円蔵370番地 三菱エン ジニアリングプラスチックス株式会社技術 センター内──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI B29K 105: 06 B29L 23:00 (72) Inventor Tatsuya Hitomi 370, Enzo 370, Chigasaki-shi, Kanagawa Mitsubishi Engineering-Plastics Corporation In the center
Claims (4)
の成形品の振動溶着時の温度を50℃以上、該ポリアミ
ド樹脂の融点未満にすることを特徴とするポリアミド樹
脂製振動溶着成形品の製造方法。1. A method of manufacturing a vibration-welded molded article made of a polyamide resin, wherein a temperature of a plurality of molded articles formed by primary molding using a polyamide resin at the time of vibration welding is set to 50 ° C. or higher and lower than the melting point of the polyamide resin. Method.
ロンまたは66/6共重合ナイロンであることを特徴と
する請求項1に記載のポリアミド樹脂製振動溶着成形品
の製造方法。2. The method according to claim 1, wherein the polyamide resin is 6 nylon, 66 nylon, or 66/6 copolymerized nylon.
ミド樹脂であることを特徴とする請求項1または2に記
載のポリアミド樹脂製振動溶着成形品の製造方法。3. The method according to claim 1, wherein the polyamide resin is a glass fiber reinforced polyamide resin.
成形品であるであることを特徴とする、請求項1ないし
3のいずれかに記載のポリアミド樹脂製振動溶着成形品
の製造方法。4. The method for producing a vibration-welded polyamide resin article according to claim 1, wherein the vibration-welded molded article made of a polyamide resin is a hollow body molded article.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8343872A JPH10180878A (en) | 1996-12-24 | 1996-12-24 | Method of manufacturing vibration welded molded product made of polyamide resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8343872A JPH10180878A (en) | 1996-12-24 | 1996-12-24 | Method of manufacturing vibration welded molded product made of polyamide resin |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10180878A true JPH10180878A (en) | 1998-07-07 |
Family
ID=18364898
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8343872A Pending JPH10180878A (en) | 1996-12-24 | 1996-12-24 | Method of manufacturing vibration welded molded product made of polyamide resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH10180878A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010023681A (en) * | 2008-07-18 | 2010-02-04 | Nakata Coating Co Ltd | Method for manufacturing vehicular interior member |
JP2012232564A (en) * | 2011-04-27 | 2012-11-29 | Branson Ultrasonics Corp | Mutual friction welding method |
-
1996
- 1996-12-24 JP JP8343872A patent/JPH10180878A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010023681A (en) * | 2008-07-18 | 2010-02-04 | Nakata Coating Co Ltd | Method for manufacturing vehicular interior member |
JP2012232564A (en) * | 2011-04-27 | 2012-11-29 | Branson Ultrasonics Corp | Mutual friction welding method |
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