Method for manufacturing diaphragm for loudspeaker

Information

  • Patent Grant
  • 6627140
  • Patent Number
    6,627,140
  • Date Filed
    Monday, May 22, 2000
    24 years ago
  • Date Issued
    Tuesday, September 30, 2003
    20 years ago
Abstract
A meshed etching tunnel made of aluminum is disposed inside a cylindrical quartz reactive chamber, and speaker diaphragms are aligned inside the tunnel at a certain interval. Opposing electrodes are disposed outside the reactive chamber. Plasma is applied at low temperature to prevent heat deformation. Uniform wettability is also assured by the use of the meshed etching tunnel, achieving high productivity. Uniform wettability further stabilizes bonding and improves bonding strength of the speaker diaphragm onto the voice coil and edge, offering a speaker with improved input power durability.
Description




FIELD OF THE INVENTION




The present invention relates to the field of methods for manufacturing speaker diaphragms employed in a range of audio equipment, speaker diaphragms made using such methods, and speakers employing such diaphragms.




BACKGROUND OF THE INVENTION




The configuration of a conventional speaker is described with reference to its sectional view in

FIG. 7. A

magnetic circuit


15


includes a magnet


15




a


, lower plate


15




b


, and upper plate


15




c.






A frame


16


is bonded to the magnetic circuit


15


. A damper


17


holds a voice coil


18


. The outer circumference of the damper


17


is bonded to the frame


16


, and its inner circumference is bonded to the voice coil


18


whose coil


18




a


is embedded in the magnetic gap


15




d


of the magnetic circuit


15


.




A speaker diaphragm


19


is bonded to the frame


16


via an edge


19




a


bonded to its outer circumference, and the inner circumference of the speaker diaphragm


19


is bonded to the voice coil


18


. This speaker diaphragm


19


is generally made mainly of paper or thin resin plates, which is selected depending on the need for weather resistance and required acoustic characteristics.




A method for manufacturing a typical speaker diaphragm


19


made of resin, more specifically a polyolefin polyethylene speaker diaphragm, is described next.




A speaker diaphragm made of polyethylene, which is a type of polyolefin system, has low material density which gives the speaker diaphragm a low mass. It also has relatively large internal loss with respect to mechanical vibration, which improves the frequency characteristic of the speaker. Accordingly, polyethylene speaker diaphragms are commonly used in speakers. However, a polyethylene speaker diaphragm has low adhesivity, making it essential to activate the surface of the speaker diaphragm to improve bonding strength.




Common conventional methods for activating the surface of the speaker diaphragm


19


include the application of primer after corona discharge, and surface treatment of the speaker diaphragm


19


by the gas plasma treatment method using parallel flat electrodes


20


and


21


as shown in

FIGS. 8 and 9

.




However, the conventional surface activating technology for treating the surface of the speaker diaphragm has the following disadvantages.




As for the method involving surface activation by corona discharge and primer application, a large processing apparatus is required because only the areas close to electrodes


20


and


21


are activated if the electrodes are small, causing a deviation in wettability of the speaker diaphragm


19


. In addition, this treatment takes about 30 seconds for one face of the speaker diaphragm


19


. The workpiece then needs to be flipped or the speaker diaphragm


19


needs to be flipped to apply treatment to the other face, requiring more than one minute for each piece and seriously degrading productivity.




Furthermore, it has another problem that the speaker diaphragm may deform during corona discharge due to high temperatures above 80° C. in the reactive chamber.




The method using the parallel flat electrode


20


in

FIG. 8

also creates the risk of heat deformation and low productivity of the speaker diaphragm


19


. The method using the parallel flat electrode


21


in

FIG. 9

may also cause low productivity. If more than one speaker diaphragm


19


is handled at once to solve the problem of low productivity, it may still have the risk of heat deformation, and significant difference in wettability between the periphery and the center.




The present invention aims to solve these disadvantages. By offering a method for manufacturing a speaker diaphragm assuring stable quality and high productivity, the present invention offers a speaker diaphragm with stable quality and a speaker employing such diaphragm.




SUMMARY OF THE INVENTION




To solve the conventional disadvantages, the method for manufacturing a speaker diaphragm of the present invention involves the next steps. A resin speaker diaphragm made by injection molding or sheet forming by heating is disposed in a reactive chamber, and electrodes are provided outside of the reactive chamber. Plasma is applied to the speaker diaphragm to activate the surface. Provision of electrodes outside the reactive chamber enables to keep the temperature of the reactive chamber below the heat deformation temperature of the speaker diaphragm during plasma treatment. Accordingly, heat deformation of the speaker diaphragm is preventable and defects caused by heat deformation can be suppressed.











BRIEF DESCRIPTION OF THE DRAWINGS





FIG. 1

is a perspective view illustrating a method for manufacturing a speaker diaphragm in an exemplary embodiment of the present invention for describing plasma treatment of the speaker diaphragm.





FIG. 2

is a sectional view illustrating the speaker diaphragm aligned in a quartz reactive chamber, which is a key part of the exemplary embodiment of the present invention.





FIG. 3

is a temperature change graph during consecutive operation of the quartz reactive chamber in the exemplary embodiment of the present invention.





FIG. 4

is a comparison of durability of wettability in the exemplary embodiment of the present invention.





FIG. 5

is a sectional view illustrating the bonding state of the speaker diaphragm and a voice coil.





FIG. 6

is a sectional view illustrating the bonding state of the speaker diaphragm and an edge.





FIG. 7

is a side sectional view of a conventional speaker.





FIG. 8

is a sectional view of an essential portion of a conventional speaker illustrating plasma treatment for the speaker diaphragm using parallel flat electrodes.





FIG. 9

is a sectional view of an essential portion of a conventional speaker illustrating plasma treatment for the speaker diaphragm in

FIG. 8

using another type of parallel flat electrodes.











DESCRIPTION OF THE PREFERRED EMBODIMENT




First Exemplary Embodiment




A method for manufacturing a speaker diaphragm in an exemplary embodiment of the present invention is described with reference to

FIGS. 1

to


6


.




The configuration of the speaker itself is the same as that of the prior art, and thus its explanation is omitted here.




In

FIGS. 1

to


6


, a meshed cylindrical aluminum etching tunnel


2


is provided inside a cylindrical quartz reactive chamber


1


. A speaker diaphragm


4


(corresponding to the speaker diaphragm


19


in the prior art) is held by a speaker diaphragm holder


3


in the reactive chamber


1


in parallel with other speaker diaphragms at approximately equal intervals. A gas inlet


6


is provided on the reactive chamber


1


, and reactive gas A flows in from this gas inlet


6


through the etching tunnel


2


formed of meshed aluminum to the reactive chamber


1


. Two pairs of electrodes


5


are provided facing each other on the outside face of the reactive chamber


1


. A gas outlet


7


is also provided.




Details of the method for manufacturing the speaker diaphragm


4


using the above reactive chamber


1


are described next Ultra high polymer polyethylene resin called“LUMBER” (product name) manufactured by Mitsui Chemicals, Inc. is used for the speaker diaphragm


4


. This“LUMBER” is formed into the speaker diaphragm


4


having a diameter of 16 cm by composite molding of injection or pressing, using an ultra high speed injection molding machine. The characteristics of this resin are shown in Table 1.
















TABLE 1













Heat deformation temperature




82




° C.







Melting point




137




° C.







Water supply rate




0.01>




%







Strength of tensile breakage point




530




kg/cm


2









Elongation of breakage point




7




%







Bending strength




18400




kg/cm


2

















It is apparent from Table 1 that this resin starts to deform at 82° C., and the speaker diaphragm


4


is exposed to the danger of deformation at the temperature 80° C. or above in the reactive chamber


1


.




The size of the quartz reactive chamber


1


is 300 mm in diameter and 500 mm in length. As shown in

FIG. 2

,


30


speaker diaphragms


4


of diameter 16 cm are aligned at 15 mm intervals. For the reactive gas A, oxygen gas is employed.




To achieve a vacuum of 0.9 torr under high frequency output of 500 W, the vacuuming time is set to 1.5 minutes, plasma treatment time to 1 minute, and the return to normal pressure 1.5 minutes, which totals about 4 minutes per cycle.

FIG. 3

shows the changes in temperature during consecutive operations under the above conditions. As shown in

FIG. 3

, the temperature inside the reactive chamber is stabilized at about 45° C. even after consecutive operation for 12 hours, and no speaker diaphragm


4


was deformed.




The wettability of the speaker diaphragm 4 obtained through the above process is 50 dyn/cm or above on any part of the speaker diaphragm


4


. This allows the assumption that plasma is applied uniformly by the use of the meshed etching tunnel


2


.




For further improving the quality, isocyanate manufactured by Takeda Chemical Industries. Ltd., called “Takenate M402” (product name) is used as the primer.

FIG. 4

shows the durability of its wettability.




It is apparent from

FIG. 4

that the wettability B immediately after treatment in the conventional method of applying primer after corona discharge is relatively high at 46 dyn/cm. However, it degrades with time, falling to about 36 dyn/cm after 200 hours.




The exemplary embodiment in which the primer is applied after plasma treatment is shown as characteristic C in FIG.


4


. It shows that the wettability immediately after treatment is a very high 50 dyn/cm, and the primer maintains a high wettability of 44 dyn/cm for considerable time, proving its stability.




Next, as shown in

FIGS. 5 and 6

, the strength was compared between the speaker diaphragm


4


to which the primer was applied after plasma treatment in this exemplary embodiment and the voice coil


18


and edge


19




a


were bonded using adhesives


12


and


13


; and the conventional speaker diaphragm to which the primer was applied after corona discharge and the voice coil and edge were bonded.




The voice coil


18


shown in

FIG. 5

has a diameter of 32 mm. The adhesive


13


is a two-part reactive acrylic adhesive, and it is used for bonding the voice coil


18


onto the speaker diaphragm


4


. The bonding strength was measured by pulling the voice coil


18


in the direction indicated by the arrow.




The edge


19




a


shown in

FIG. 6

is made of rubber, and it is bonded to the speaker diaphragm


4


using the adhesive


12


which is butyl rubber solvent adhesive. The peeling strength was tested using a bonding area of 25 mm wide and 5 mm long.




A 016 cm speaker was then made using the above Ø32 voice coil


18


and edge


19




a


, and the input power durability was tested. Table 2 shows the results of each test.















TABLE 2











plasma treatment




corona discharge




























cone  voice coil




 18 kg




 11 kg







cone  edge




4.5 kg




2.5 kg







input power durability




120 W




70 W







(breakage mode)




damage to voice coil




peeling of bonding















It is apparent from Table 2 that the speaker diaphragm of the exemplary embodiment which uses plasma treatment has better bonding strength than the conventional speaker diaphragm using corona discharge.




In the input power durability test, the bonded area has peeled off in the conventional speaker using corona discharge by input of 70 W. In the exemplary embodiment using plasma processing, burning of the voice coil


18


occurred by input of 120 W. However, no peeling of the bonded area has occurred, demonstrating extremely high bonding strength.




As for the reactive gas A, approximately the same results as for oxygen were obtained by the use of nitrogen gas or air. As for the material of the speaker diaphragm


4


, approximately the same effect was obtained with polypropylene or nylon resin.




As described above, the exemplary embodiment provides electrodes


5


outside the reactive chamber


1


for plasma treatment. This enables the suppression of temperature rise in the reactive chamber


1


and prevents heat deformation of the speaker diaphragm


4


. In addition, plasma can be uniformly applied by placing the speaker diaphragm


4


in a meshed metal frame, resulting in improved productivity.




Industrial Applicability




The method for manufacturing a speaker diaphragm of the present invention disposes a resin speaker diaphragm made by injection molding or sheet forming by heating in the reactive chamber, and provides electrodes outside the reactive chamber. This enables the temperature inside the reactive chamber to be kept below the heat deformation temperature of the speaker diaphragm during surface activation of the speaker diaphragm by application of plasma. The temperature inside the reactive chamber is kept below the heat deformation temperature of the speaker diaphragm to prevent heat deformation of the speaker diaphragm and to suppress the occurrence of defects caused by heat deformation.




In addition, more than one speaker diaphragm is disposed inside the meshed metal frame in the reactive chamber at a predetermined interval to apply plasma almost uniformly. The gas disperses almost uniformly inside the reactive chamber through the meshed metal frame so that the surface is almost uniformly activated, assuring high wettability and stable high quality of the speaker diaphragm.




Moreover, application of isocyanate primer after plasma treatment further improves the bonding strength and stabilizes the quality.




The material used for the speaker diaphragm of the present invention is a monopolymer or copolymer of polyolefin resin such as polyethylene and polypropylene, or monopolymer or copolymer of polyamide resin. This enables a broad range of speaker diaphragms with improved bonding strength and stable quality to be manufactured.




A speaker manufactured using the speaker diaphragm manufactured as above thus has uniform and improved bonding strength between the speaker diaphragm and edge and/or voice coils, offering speakers with improved input power durability.




Reference Numerals






1


reactive chamber






2


etching tunnel






3


speaker diaphragm holder






4


speaker diaphragm






5


electrode






6


gas inlet






7


gas outlet






12


adhesive






13


adhesive






15


magnetic circuit






15




a


magnet






15




b


lower plate






15




c


upper plate






16


frame






17


damper






18


voice coil






18




a


coil






19


speaker diaphragm






19




a


edge






20


parallel flat electrode






21


parallel flat electrode



Claims
  • 1. A method for manufacturing a diaphragm for a loudspeaker, comprising the steps of:heating a molded resin diaphragm for said loudspeakers in a reactive chamber; and activating the surface of said diaphragm for said loudspeaker by applying plasma while keeping the temperature inside said reactive chamber below a heat deformation temperature of said diaphragm for said loudspeaker.
  • 2. The method for manufacturing a diaphragm for a loudspeaker as defined in claim 1, wherein a plurality of molded resin speaker diaphragms are placed inside said reactive chamber at a certain interval so as to apply plasma substantially uniformly.
  • 3. The method for manufacturing a diaphragm for a loudspeaker as defined in claim 1, wherein isocyanate primer is applied after plasma treatment.
  • 4. The method for manufacturing a diaphragm for a loudspeaker as defined in claim 2, wherein isocyanate primer is applied after plasma treatment.
  • 5. The method for manufacturing a diaphragm for a loudspeaker as defined in claim 1, wherein one of monopolymer and copolymer of polyolefin such as polyethylene and polypropylene is used as a material for said diaphragm for said loudspeaker.
  • 6. The method for manufacturing a diaphragm for a loudspeaker as defined in claim 2, wherein one of monopolymer and copolymer of polyolefin such as polyethylene and polypropylene is used as a material for said diaphragm for said loudspeaker.
  • 7. The method for manufacturing a diaphragm for a loudspeaker as defined in claim 3, wherein one of monopolymer and copolymer of polyolefin such as polyethylene and polypropylene is used as a material for said diaphragm for said loudspeaker.
  • 8. The method for manufacturing a diaphragm for a loudspeaker as defined in claim 4, wherein one of monopolymer and copolymer of polyolefin such as polyethylene and polypropylene is used as a material for said diaphragm for said loudspeaker.
  • 9. The method for manufacturing a loudspeaker diaphragm as; defined in claim 1, further comprising the step of manufacturing said molded resin speaker diaphragm by one of injection molding and sheet forming.
  • 10. The method of manufacturing a loudspeaker diaphragm as defined in claim 1, wherein said reactive chamber is disposed with a meshed metal frame inside said reactive chamber and with an electrode outside said reactive chamber.
Priority Claims (1)
Number Date Country Kind
10-164892 Jun 1998 JP
Parent Case Info

THIS APPLICATION IS A U.S. NATIONAL PHASE APPLICATION OF PCT INTERNATIONAL APPLICATION PCT/JP99/03140filed on Jun. 11, 1999.

PCT Information
Filing Document Filing Date Country Kind
PCT/JP99/03140 WO 00
Publishing Document Publishing Date Country Kind
WO99/65272 12/16/1999 WO A
Foreign Referenced Citations (3)
Number Date Country
60048696 Mar 1985 JP
5-168903 Feb 1993 JP
6-225388 Aug 1994 JP
Non-Patent Literature Citations (2)
Entry
Japanese search report for PCT/JP99/03140 dated Aug. 24, 1999.
English translation of Form PCT/ISA/210(Aug. 24, 1999).