Method for making conductive polymer, and composite film and circuit board having the conductive polymer
09807868 · 2017-10-31
Assignee
- Avary Holding (Shenzhen) Co., Limited. (Shenzhen, CN)
- HongQiSheng Precision Electronics (QinHuangDao) Co.,Ltd. (Qinhuangdao, CN)
Inventors
Cpc classification
C09K19/04
CHEMISTRY; METALLURGY
C09D125/18
CHEMISTRY; METALLURGY
H05K2201/0329
ELECTRICITY
H05K1/0219
ELECTRICITY
C09K2019/0448
CHEMISTRY; METALLURGY
H05K1/115
ELECTRICITY
C08L25/18
CHEMISTRY; METALLURGY
C09D125/18
CHEMISTRY; METALLURGY
C08L25/18
CHEMISTRY; METALLURGY
H05K1/09
ELECTRICITY
International classification
C09D125/18
CHEMISTRY; METALLURGY
H05K1/09
ELECTRICITY
Abstract
A method for making a conductive polymer for electromagnetic shielding purposes includes steps of mixing liquid crystal monomers, a silver complex, an initiator, and a catalytic agent in certain proportions by weight to form a mixture. A solvent is added into the mixture, the mixture and the solvent being in a ratio from 3:17 to 1:3 by weight. The mixture is heated to undergo an atom transfer radical polymerization.
Claims
1. A method for making a conductive polymer comprising: mixing liquid crystal monomers, a silver complex, an initiator, and a catalytic agent to form a mixture, the liquid crystal monomers having a mass percentage of about 42.2% to about 52.2% of a total mass of the mixture, the silver complex having a mass percentage of about 43.1% to about 53.1% of the total mass of the mixture, the initiator having a mass percentage of about 0.85% to about 1.35% of the total mass of the mixture, and the catalytic agent having a mass percentage of about 2.85% to about 4.35% of the total mass of the mixture; adding a solvent into the mixture, the mixture and the solvent being in a ratio from 3:17 to 1:3 by weight; and heating the mixture to undergo atom transfer radical polymerization.
2. The method of claim 1, wherein the liquid crystal monomers are selected from a group consisting of 2,5-bis[(4methoxyphenyl)oxycarbonyl]styrene, 4-vinyl benzene and derivant thereof, methyl acrylate, hydroxyethyl acrylate, vinyl acrylate, N,N-dimethylamino propenyl ketone, acrylonitrile, methyl methacrylate, butyl methacrylate, N,N-dimethylaminoethyl methacrylate, and tert-butyl methacrylate.
3. The method of claim 1, wherein the silver complex is selected from a group consisting of AgNO.sub.3, Ag.sub.2O, AgBP.sub.4, and AgPF.sub.6.
4. The method of claim 1, wherein the initiator is selected from a group consisting of 1,3,5-(2′-bromo-2-methylpropionato)benzene, α-bromine ethane, 2-ethyl bromide, 2-bromine-2-methyl ethyl propionate, and 2-dibromine propionitrile.
5. The method of claim 1, wherein the catalytic agent is copper bromide.
6. The method of claim 1, wherein the catalytic agent is copper bromide and sparteine.
7. The method of claim 1, wherein the solvent is selected from a group consisting of dimethyl sulfoxide, dimethylformamide, and N-methyl-2-pyrrolidone.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) Implementations of the present technology will now be described, by way of example only, with reference to the attached figures.
(2)
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DETAILED DESCRIPTION
(12) It will be appreciated that for simplicity and clarity of illustration, where appropriate, reference numerals have been repeated among the different figures to indicate corresponding or analogous elements. In addition, numerous specific details are set forth in order to provide a thorough understanding of the exemplary embodiments described herein. However, it will be understood by those of ordinary skill in the art that the exemplary embodiments described herein can be practiced without these specific details. In other instances, methods, procedures, and components have not been described in detail so as not to obscure the related relevant feature being described. Also, the description is not to be considered as limiting the scope of the exemplary embodiments described herein. The drawings are not necessarily to scale and the proportions of certain parts may be exaggerated to better illustrate details and features of the present disclosure.
(13) The term “comprising,” when utilized, means “including, but not necessarily limited to”; it specifically indicates open-ended inclusion or membership in the so-described combination, group, series, and the like.
(14) An exemplary embodiment of a conductive polymer which can be used in a circuit board is described. The conductive polymer is made by heating a mixture comprising liquid crystal monomers, a silver complex, an initiator, and a catalytic agent, and a solvent, to cause the mixture to undergo an atom transfer radical polymerization (ATRP). The liquid crystal monomers have a mass percentage of about 42.2% to about 52.2% of a total mass of the mixture. The silver complex has a mass percentage of about 43.1% to about 53.1% of the total mass of the mixture. The initiator has a mass percentage of about 0.85% to about 1.35% of the total mass of the mixture. The catalytic agent has a mass percentage of about 2.85% to about 4.35% of the total mass of the mixture. The mixture and the solvent are in a ratio from 3:17 to 1:3 by weight. After the atom transfer radical polymerization, the silver complex is wrapped in the conductive polymer which causes the conductive polymer to be electrically conductive.
(15) The liquid crystal monomers are selected from a group consisting of 2,5-bis[(4methoxyphenyl)oxycarbonyl]styrene
(16) ##STR00001##
4-vinyl benzene and derivant thereof
(17) ##STR00002##
R can be H, Me, t-Bu, Br, F, CF.sub.3, or OAc), methyl acrylate
(18) ##STR00003##
hydroxyethyl acrylate
(19) ##STR00004##
vinyl acrylate
(20) ##STR00005##
N,N-dimethylamino propenyl ketone
(21) ##STR00006##
acrylonitrile
(22) ##STR00007##
methyl methacrylate
(23) ##STR00008##
butyl methacrylate
(24) ##STR00009##
N,N-dimethylaminoethyl methacrylate
(25) ##STR00010##
and tert-butyl methacrylate
(26) ##STR00011##
In at least one exemplary embodiment, the liquid crystal monomers are 2,5-bis[(4methoxyphenyl)oxycarbonyl]styrene which can cause the conductive polymer to form side chains for wrapping the silver complex in the conductive polymer.
(27) The silver complex can be selected from a group consisting of silver nitrate (AgNO.sub.3), silver oxide (Ag.sub.2O), AgBP.sub.4, and AgPF.sub.6. In at least one exemplary embodiment, the silver complex is silver nitrate.
(28) The initiator can be selected from a group consisting of 1,3,5-(2′-bromo-2-methylpropionato)benzene
(29) ##STR00012##
α-bromine ethane
(30) ##STR00013##
2-ethyl bromide
(31) ##STR00014##
2-bromine-2-methyl ethyl propionate
(32) ##STR00015##
and 2-dibromine propionitrile
(33) ##STR00016##
In other exemplary embodiments, the initiator can be other halides such as other alkyl halides, benzyl halides, α-bromine compounds, α-haloketones, α-halogen halides, aryl sulfonyl chloride, or azobisisobutyronitrile. In at least one exemplary embodiment, the initiator is 1,3,5-(2′-bromo-2-methylpropionato)benzene which can cause the conductive polymer to form side chains for wrapping the silver complex in the conductive polymer.
(34) The catalytic agent can be copper bromide (CuBr). In other exemplary embodiments, the catalytic agent can be copper bromide and sparteine.
(35) The solvent can be selected from a group consisting of dimethyl sulfoxide (DMSO), dimethylformamide (DMF), and N-methyl-2-pyrrolidone (NMP). In at least one exemplary embodiment, the solvent is N-methyl-2-pyrrolidone.
(36) An exemplary embodiment of a method for making the conductive polymer comprises the following steps. The liquid crystal monomers, the silver complex, the initiator, and the catalytic agent are mixed to form a mixture. The solvent is added into the mixture, and the mixture is heated to undergo atom transfer radical polymerization.
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(38) The composite film 10 can further comprise an adhesive layer 15 in contact with a surface of the base layer 11, which is opposite to the active surface 111.
(39) Referring to
(40) At step 1, referring to
(41) At step 2, referring to
(42) At step 3, referring to
(43) At step 4, referring to
(44) At step 5, referring to
(45) At step 6, referring to
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(47) In at least one exemplary embodiment, the flexible board 20 is a double-sided board which comprises the substrate 21 and two conductive wiring layers 23 formed on opposite surfaces of the substrate 21.
(48) In at least one exemplary embodiment, the circuit board 100 further comprises the solder mask layer 40. The solder mask layer 40 covers the copper layer 30, the inner wall and the bottom surface of the through hole 101.
EXAMPLE
(49) 2,5-bis[(4methoxyphenyl)oxycarbonyl]styrene of 105.9 g, AgNO.sub.3 of 108 g, 1,3,5-(2′-bromo-2-methylpropionato)benzene of 2.5 g, CuBr of 1.9 g, and sparteine of 6.1 g were mixed to form a mixture. 864 g of NMP was added into the mixture and heated under 90 □ to form a conductive polymer. A composite film 10 was made by using the conductive polymer. A circuit board 100 was made by using a flexible board 20, the composite film 10, a copper layer 30, and a solder mask layer 40.
COMPARATIVE EXAMPLE
(50) A circuit board was made by using a flexible board 20 and a conventional electromagnetic shielding layer. The electromagnetic shielding layer comprises an adhesive layer, a copper layer 30, and a solder mask layer 40. The adhesive layer has a thickness equaling that of the composite film 10 of the above example.
(51) The signal waveforms from the circuit board 100 of the example above for transmitting signals at 5 Gbps and 10 Gbps were tested to obtain the eye patterns shown in
(52) It is to be understood, even though information and advantages of the present embodiments have been set forth in the foregoing description, together with details of the structures and functions of the present embodiments, the disclosure is illustrative only; changes may be made in detail, especially in matters of shape, size, and arrangement of parts within the principles of the present embodiments to the full extent indicated by the plain meaning of the terms in which the appended claims are expressed.