JPH0423875A - Adhesive composition for temporary fixation - Google Patents
Adhesive composition for temporary fixationInfo
- Publication number
- JPH0423875A JPH0423875A JP12945690A JP12945690A JPH0423875A JP H0423875 A JPH0423875 A JP H0423875A JP 12945690 A JP12945690 A JP 12945690A JP 12945690 A JP12945690 A JP 12945690A JP H0423875 A JPH0423875 A JP H0423875A
- Authority
- JP
- Japan
- Prior art keywords
- water
- component
- adhesive composition
- double bond
- ethylenic double
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 23
- 239000000853 adhesive Substances 0.000 title claims description 25
- 230000001070 adhesive effect Effects 0.000 title claims description 25
- 239000003505 polymerization initiator Substances 0.000 claims abstract description 6
- 239000000178 monomer Substances 0.000 claims abstract description 4
- 238000005476 soldering Methods 0.000 claims description 11
- 239000011256 inorganic filler Substances 0.000 claims description 5
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 10
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 abstract description 2
- 239000002202 Polyethylene glycol Substances 0.000 abstract description 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract description 2
- 229920003169 water-soluble polymer Polymers 0.000 abstract 3
- 229920003176 water-insoluble polymer Polymers 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
- 229910000679 solder Inorganic materials 0.000 description 5
- 239000000945 filler Substances 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 4
- -1 Amino ( meth)acrylic acid Chemical compound 0.000 description 3
- 239000004830 Super Glue Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000007717 redox polymerization reaction Methods 0.000 description 3
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- 229920002845 Poly(methacrylic acid) Chemical class 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000000783 alginic acid Substances 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 229960001126 alginic acid Drugs 0.000 description 2
- 150000004781 alginic acids Chemical class 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920000609 methyl cellulose Chemical class 0.000 description 2
- 239000001923 methylcellulose Chemical class 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- BGGPWYUMZXIUBW-UHFFFAOYSA-N 1,2,3-trichlorothioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C=C(Cl)C(Cl)=C2Cl BGGPWYUMZXIUBW-UHFFFAOYSA-N 0.000 description 1
- NFTVTXIQFYRSHF-UHFFFAOYSA-N 1-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)C(C)OC(=O)C=C NFTVTXIQFYRSHF-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Chemical class 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000001856 Ethyl cellulose Chemical class 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical class CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Chemical class 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Chemical class 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229920006187 aquazol Polymers 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 239000001768 carboxy methyl cellulose Chemical class 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- SPTHWAJJMLCAQF-UHFFFAOYSA-M ctk4f8481 Chemical compound [O-]O.CC(C)C1=CC=CC=C1C(C)C SPTHWAJJMLCAQF-UHFFFAOYSA-M 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- REQPQFUJGGOFQL-UHFFFAOYSA-N dimethylcarbamothioyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SC(=S)N(C)C REQPQFUJGGOFQL-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229920001249 ethyl cellulose Chemical class 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- FGBJXOREULPLGL-UHFFFAOYSA-N ethyl cyanoacrylate Chemical compound CCOC(=O)C(=C)C#N FGBJXOREULPLGL-UHFFFAOYSA-N 0.000 description 1
- 229940053009 ethyl cyanoacrylate Drugs 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- YLHXLHGIAMFFBU-UHFFFAOYSA-N methyl phenylglyoxalate Chemical compound COC(=O)C(=O)C1=CC=CC=C1 YLHXLHGIAMFFBU-UHFFFAOYSA-N 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/30—Assembling printed circuits with electric components, e.g. with resistor
- H05K3/303—Surface mounted components, e.g. affixing before soldering, aligning means, spacing means
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Electric Connection Of Electric Components To Printed Circuits (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は■、C等の電子部品をプリント基板上にハンダ
付けする前に該電子部品の仮固定用として使用される接
着剤組成物に係り、特に、仮固定後、ハンダ付けの際に
電子部品のずれや脱落が起こらず、しかも仮固定された
電子部品を交換等のために取りはずす際に水ないしは温
水等に浸漬するのみで容易にかつ速やかに取りはずすこ
とができ、かつプリント基板上に残存している接着剤を
も容易に除去することができる仮固定用接着剤組成物に
関する。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to an adhesive composition used for temporarily fixing electronic components such as (1) and (C) before soldering them onto a printed circuit board. In particular, after temporarily fixing, the electronic components do not shift or fall off during soldering, and when the temporarily fixed electronic components are removed for replacement etc., they can be easily removed by simply immersing them in water or hot water. The present invention also relates to an adhesive composition for temporary fixing that can be quickly removed and that can also easily remove adhesive remaining on a printed circuit board.
1、C等の電子部品をプリント基板上にノ\ンダ付けす
る際には、まずハンダ付けの前に電子部品のずれや脱落
を防止するために該電子部品の仮固定が必要である。When soldering electronic components such as 1 and C onto a printed circuit board, it is first necessary to temporarily fix the electronic components to prevent them from shifting or falling off before soldering.
このような仮固定のための接着剤として、従来、シアノ
アクリレート系接着剤が用いられていた。Conventionally, cyanoacrylate adhesives have been used as adhesives for such temporary fixing.
しかし、この接着剤では電子部品とプリント基板のすき
間から接着剤が流れ出てしまい、このため仮固定が不充
分となってハンダ付けの際に電子部品のずれや脱落が起
こり、ハンダ付は作業が困難となる。However, with this adhesive, the adhesive flows out from the gap between the electronic component and the printed circuit board, resulting in insufficient temporary fixation and causing the electronic component to shift or fall off during soldering, making the soldering process difficult. It becomes difficult.
また、電子部品をプリント基板上に仮固定の後、修理等
のためにこの交換を余儀なくされる場合に、電子部品を
プリント基板から取りはずさなければならなくなる。し
かし、この取りはすしのためには150℃の温度で数十
分程度の加熱が必要となり、取りはずし作業が厄介とな
るばかりでなく、この熱により電子部品が変質したり、
破損したり等の損失を受ける。また、電子部品を取りは
ずした後にもプリント基板上に残存している接着剤を有
機溶剤により洗浄して除去しなければならず、この点か
らも取りはずし作業が厄介であるということができ、さ
らに有機溶剤による作業環境の悪化を紹くことになる。Further, after the electronic component is temporarily fixed on the printed circuit board, if the electronic component must be replaced for repair or the like, the electronic component must be removed from the printed circuit board. However, this removal requires heating at a temperature of 150°C for several tens of minutes for sushi, which not only makes the removal work troublesome, but also causes the electronic parts to deteriorate due to this heat.
damage or other losses. Furthermore, even after removing electronic components, the adhesive remaining on the printed circuit board must be removed by cleaning with an organic solvent, which also makes the removal process troublesome. This will introduce the deterioration of the working environment caused by solvents.
そこで、本発明の目的は電子部品をプリント基板上に仮
固定の後、ハンダ付けの際に電子部品のずれや脱落が起
こらず、しかも仮固定された電子部品を交換等のために
プリント基板から取りはずす際に水ないしは温水等に浸
漬するのみで容易にかつ速やかに取りはずしが可能であ
り、プリント基板上の残存接着剤をも洗浄除去され、前
述の公知技術に存する欠点を改良した仮固定用接着剤組
成物を提供することにある。Therefore, an object of the present invention is to prevent the electronic components from shifting or falling off during soldering after temporarily fixing the electronic components on the printed circuit board, and to remove the temporarily fixed electronic components from the printed circuit board for replacement etc. This adhesive for temporary fixing can be easily and quickly removed by simply immersing it in water or hot water, and any residual adhesive on the printed circuit board can be washed away, improving the shortcomings of the aforementioned known technologies. An object of the present invention is to provide a drug composition.
前述の目的を達成するため、本発明によれば、電子部品
をプリント基板上にハンダ付けする前に該電子部品の仮
固定用として使用される接着剤組成物において、次の成
分(A)、(B)、(C)および(ロ)すなわち、
(A)分子内に重合可能なエチレン性二重結合を少なく
とも一つ有し、かつ重合物が吸水性または水溶性となり
得るモノマー
(B)吸水性および/または水溶性高分子物質。In order to achieve the above-mentioned object, according to the present invention, in an adhesive composition used for temporarily fixing electronic components before soldering the electronic components onto a printed circuit board, the following components (A), (B), (C) and (b) That is, (A) A monomer that has at least one polymerizable ethylenic double bond in the molecule and whose polymer can become water-absorbing or water-soluble (B) Water-absorbing water-soluble and/or water-soluble polymeric substances.
(C)分子内にエチレン性二重結合を少なくとも一つ有
し、かつ重合物が非吸水性または非水溶性となり得るオ
リゴマ−またはプレポリマー(D)重合開始剤。(C) An oligomer or prepolymer having at least one ethylenic double bond in the molecule and capable of making the polymer non-water-absorbing or water-insoluble. (D) A polymerization initiator.
を含むことを特徴とし、さらに本発明によれば、上述の
成分(A)、(B)、(C)および(D)に加えて、成
分(E)として無機充填剤を含むことを特徴とする。Further, according to the present invention, in addition to the above-mentioned components (A), (B), (C) and (D), it contains an inorganic filler as component (E). do.
前述の成分(A)として具体的には例えば、N−ビニル
−2−ピロリドン、N、N−ジアルキルアミノアルキル
(メタ)アクリル酸、例えばN%N−ジメチルアミノエ
チルアクリレート等、N、 N−ジアルキルアミノ (
メタ)アクリル酸アミド、例えばN、N−ジアクリル酸
アミド等、N−Nジアルキルアミノアルキル(メタ)ア
クリル酸アミド、例えばN、N−ジメチルアミノプロピ
ルアクリル酸アミド、N−N−ジメチルアミノプロピル
メタアクリル酸アミド等が挙げられる。Specific examples of the aforementioned component (A) include N-vinyl-2-pyrrolidone, N,N-dialkylaminoalkyl (meth)acrylic acid, such as N%N-dimethylaminoethyl acrylate, and N,N-dialkyl. Amino (
meth)acrylic acid amides, such as N,N-diacrylic acid amide; Examples include acid amides.
前記成分(B)として成分(A)の千ツマ−の単独重合
体、共重合体の他に、例えば、ポリエチレングリコール
、ポリエチレンオキサイド、アルギン酸、アルギン酸の
塩、カルボキシメチルセルロース、ヒドロキシエチルセ
ルロース、メチルセルロース、メチルセルロース、エチ
ルセルロース、ポリ (メタ)アクリル酸、ポリ (メ
タ)アクリル酸の塩、ポリビニルアルコール、ポリビニ
ルエーテル、ポリエチルオキサゾリン、ビニルピロリド
ン酢酸ビニル共重合体、メチルビニルエーテル無水マレ
イン酸共重合体、デンプン、ゼラチン、寒天等が挙げら
れる。これらの成分(日)は前記成分(A)に溶解する
ことが好ましいが、全くあるいは部分的に不溶で成分(
A)中に分散するものであってもよい。なお、成分(B
)は吸水性と水溶性の両方の性質を存する物質であって
もよく、いずれか単独の性質のものであってもよい。In addition to the homopolymers and copolymers of component (A), the component (B) may include, for example, polyethylene glycol, polyethylene oxide, alginic acid, salts of alginic acid, carboxymethylcellulose, hydroxyethylcellulose, methylcellulose, methylcellulose, Ethylcellulose, poly(meth)acrylic acid, salts of poly(meth)acrylic acid, polyvinyl alcohol, polyvinyl ether, polyethyloxazoline, vinylpyrrolidone-vinyl acetate copolymer, methyl vinyl ether maleic anhydride copolymer, starch, gelatin, agar etc. It is preferable that these components are dissolved in the component (A), but are completely or partially insoluble and are dissolved in the component (A).
A) may be dispersed in the material. In addition, component (B
) may be a substance that has both water-absorbing and water-soluble properties, or may have either property alone.
前記成分(C)として具体的には、例えば、イソボロニ
ル(メタ)アクリレート、ジシクロペンテニル(メタ)
アクリレート、ジシクロペンタニル(メタ)アクリレー
ト、ジシクロペンテニルオキシエチル(メタ)アクリレ
ート、1.6−ヘキサンシオールジ(メタ)アクリレー
ト、ペンタエリスリトールトリ (メタ)アクリレート
、トリス〔2−(メタ)アルリロキシエチル〕イソシア
ヌレート、ジペンタエリスリトールモノヒドロキシペン
タ(メタ)アクリレート、ビスフェノールAエポキシ(
メタ)アクリレート等があげられる。Specifically, the component (C) is, for example, isobornyl (meth)acrylate, dicyclopentenyl (meth)
Acrylate, dicyclopentanyl (meth)acrylate, dicyclopentenyloxyethyl (meth)acrylate, 1,6-hexanethiol di(meth)acrylate, pentaerythritol tri(meth)acrylate, tris[2-(meth)ally [oxyethyl] isocyanurate, dipentaerythritol monohydroxypenta(meth)acrylate, bisphenol A epoxy (
Examples include meta)acrylate.
また、前記成分(D) として例えば、光重合開始剤、
レドックス系重合開始剤等が挙げられ、前記光重合開始
剤として具体的には、例えば、ベンゾフェノン、アセト
フェノン、ミヒラーズケトン、ベンジル、ベンゾイン、
ベンゾインメチルエーテル、ベンゾインエチルエーテル
、テトラメチルチウラムスルフィド、チオキサントリク
ロロチオキサントン、ベンジルジメチルケタール、メチ
ルベンゾイルフォーメート等が挙げられ、またこれら光
重合開始剤と併せて必要に応じて、増感剤を用いること
もできる。前記レドックス系重合開始剤は有機過酸化物
と還元剤を含むレドックス系触媒で、例えば、メチルエ
チルケトンパーオキサイド、メチルシクロヘキサノンパ
ーオキサイド等のケトンパーオキサイドとナフテン酸コ
バルト、ナフテン酸銅等の金属石鹸との組み合わせ、ま
たはオクタノイルパーオキサイド、ベンゾイルパーオキ
サイド等のジアシルパーオキサイドと、N、N−ジメチ
ルアニリン、N、N−ジメチル−P−)ルイジン等の3
級アミンとの組み合わせ、またはクメンハイドロパーオ
キサイド、ジイソプロピルベンゼンハイドロパーオキサ
イド等のハイドロパーオキサイドと、チオ尿素、エチレ
ンチオ尿素等の有機チオ尿素との組み合わせ等が挙げら
れる。なお、成分(D)は光重合開始剤とレドックス系
重合開始剤の併用も可能である。Further, as the component (D), for example, a photopolymerization initiator,
Examples of the photopolymerization initiator include redox polymerization initiators, such as benzophenone, acetophenone, Michler's ketone, benzyl, benzoin,
Examples include benzoin methyl ether, benzoin ethyl ether, tetramethylthiuram sulfide, thioxane trichlorothioxanthone, benzyl dimethyl ketal, methyl benzoyl formate, and in addition to these photopolymerization initiators, a sensitizer may be used as necessary. You can also do that. The redox polymerization initiator is a redox catalyst containing an organic peroxide and a reducing agent, such as a combination of a ketone peroxide such as methyl ethyl ketone peroxide or methyl cyclohexanone peroxide and a metal soap such as cobalt naphthenate or copper naphthenate. combination, or diacyl peroxide such as octanoyl peroxide, benzoyl peroxide, and 3 such as N,N-dimethylaniline, N,N-dimethyl-P-)luidine, etc.
Examples include a combination with a grade amine, or a combination of a hydroperoxide such as cumene hydroperoxide or diisopropylbenzene hydroperoxide with an organic thiourea such as thiourea or ethylenethiourea. Note that component (D) can also be a combination of a photopolymerization initiator and a redox polymerization initiator.
前記成分(A)成分および(B)の配合比率は任意であ
るが、粘度を高める場合には成分(B)を多く配合し、
低める場合には成分(B)を少なく配合し、成分(B)
の配合量を変化させることにより所望の粘度に調整され
る。The blending ratio of the components (A) and (B) is arbitrary, but in order to increase the viscosity, a large amount of component (B) is blended,
To lower the amount of component (B), add less component (B).
The desired viscosity can be adjusted by changing the amount of .
前記成分(C)の添加量は成分(A)と成分(B)の合
計量100重量部に対し、0.1〜25重量部であり、
好ましくは5〜15重量部である。少なすぎるとハンダ
付けの際電子部品のずれや脱落がおこり、また多すぎる
と硬化物の水溶性が低下し、電子部品を取りはずす際の
作業性が低下する。The amount of component (C) added is 0.1 to 25 parts by weight per 100 parts by weight of the total amount of component (A) and component (B),
Preferably it is 5 to 15 parts by weight. If it is too small, the electronic components may shift or fall off during soldering, and if it is too large, the water solubility of the cured product decreases, reducing workability when removing the electronic components.
また、前記成分印)の添加量は成分(A)と成分(B)
の合計量10000重量部し、0. OL−・10重量
部であり、好ましくは1〜5重量部である。In addition, the amount of the above component mark) is for component (A) and component (B).
A total amount of 10,000 parts by weight, 0. OL-.10 parts by weight, preferably 1 to 5 parts by weight.
本発明は前記成分(A)、(B)、(C)および(D)
に加え、さらに無機充填剤を含むことにより、接着剤組
成物の粘度調整が一層容易となる。また、接着剤組成物
への揺変性の付与が可能になり、接着剤を取り扱う際の
作業性を向上することができる。The present invention comprises the components (A), (B), (C) and (D).
In addition to this, by further containing an inorganic filler, it becomes easier to adjust the viscosity of the adhesive composition. Further, it becomes possible to impart thixotropy to the adhesive composition, and workability when handling the adhesive can be improved.
このような無機系充填剤としては、シリカ系充填剤等の
ような水に分散する充填剤が好ましく、より好ましくは
充填剤粒子表面の水酸基が残留している充填剤が好適で
あるが、特に限定はされない。As such an inorganic filler, a water-dispersible filler such as a silica filler is preferable, and a filler in which hydroxyl groups remain on the surface of the filler particles is more preferable. There are no limitations.
さらに本発明は必要に応じて、重合禁止剤、例えば、ハ
イドロキノン、カテコール、2.6−ジtert−ブチ
ル−P−クレゾール等を保存安定性向上の目的で用いる
ことができる。Furthermore, in the present invention, a polymerization inhibitor such as hydroquinone, catechol, 2,6-di-tert-butyl-P-cresol, etc. can be used for the purpose of improving storage stability, if necessary.
上述の本発明組成物は成分(A)に対する成分(B)の
配合量の変化により粘度を自由に調整し得、このため、
例えば電子部品が反っていて、これとプリント基板との
間にすき間が大きく形成されても、粘度を高く調整する
ことによりすき間内に保持され、従来のシアノアクリレ
ート接着剤のようにすき間から流れ出てしまうようなこ
とがなく、仮固定が充分となって電子部品のずれや脱落
を起こさない。さらに成分(A)、(B)、(C)の配
合により仮固定の接着強度が増加してハンダ付けの際に
電子部品のずれや脱落が防止され、かつ硬化物の吸水性
ないしは水溶性が増加し、電子部品を取りはずす廉に作
業性が向上する。The viscosity of the above-mentioned composition of the present invention can be freely adjusted by changing the blending amount of component (B) with respect to component (A), and therefore,
For example, even if an electronic component is warped and a large gap is formed between it and the printed circuit board, adjusting the viscosity to a high level will hold it in the gap and prevent it from flowing out of the gap like traditional cyanoacrylate adhesives. There is no storage, and temporary fixation is sufficient to prevent electronic components from shifting or falling off. Furthermore, the combination of components (A), (B), and (C) increases the adhesive strength for temporary fixing, prevents electronic components from shifting or falling off during soldering, and increases the water absorption or water solubility of the cured product. This increases work efficiency by eliminating the need to remove electronic components.
また、本発明組成物に無機充填剤を配合することにより
上記粘度調整が一層容易となり、かつ本発明接着剤組成
物への揺変性の付与が可能となり、取り扱う際の作業性
が向上する。Furthermore, by incorporating an inorganic filler into the composition of the present invention, the above-mentioned viscosity adjustment becomes easier, and it becomes possible to impart thixotropy to the adhesive composition of the present invention, thereby improving workability during handling.
以下の表−1に示す配合の接着剤組成物試料Nα1〜5
を混合、調整した。このうち試料Nα1〜2は本発明に
かかる組成物(実施例)であり、試料Nα3〜5は比較
例であり、特に試料N(L5は従来のエチルシアノアク
リレート接着剤単独である。Adhesive composition samples Nα1 to 5 with the formulation shown in Table 1 below
mixed and adjusted. Among these, samples Nα1-2 are compositions according to the present invention (examples), samples Nα3-5 are comparative examples, and in particular sample N (L5 is a conventional ethyl cyanoacrylate adhesive alone).
表−1の各試料接着剤を用いてそれぞれ第1図および第
2図に示されるような仮固定試験を行った。Temporary fixation tests as shown in FIGS. 1 and 2 were conducted using each of the sample adhesives shown in Table 1.
第1図は電子部品のプリント基板への仮固定状態を示す
平面図であり、第2図は第1図の断面図である。第1図
および第2図に示されるように、プリント基板1上に表
−1の各試料Nα1〜5の接着剤2をそれぞれ塗布し、
この上に電子部品3を載置した。次いで試料Nα1〜4
に対してそれぞれ高圧水銀灯(4KW)により高さ15
cmから紫外線を20秒間照射して電子部品3をプリン
ト基板1上に仮固定した。試料嵐5については湿度60
%、温度25℃の条件下に24時間放置して仮固定した
。FIG. 1 is a plan view showing a state in which an electronic component is temporarily fixed to a printed circuit board, and FIG. 2 is a sectional view of FIG. 1. As shown in FIGS. 1 and 2, adhesives 2 of each sample Nα1 to 5 in Table 1 are applied on a printed circuit board 1,
The electronic component 3 was placed on top of this. Next, samples Nα1 to 4
15 in height using a high-pressure mercury lamp (4KW).
The electronic component 3 was temporarily fixed on the printed circuit board 1 by irradiating the electronic component 3 with ultraviolet rays from a cm wavelength for 20 seconds. Humidity 60 for sample Arashi 5
%, and was temporarily fixed by being left for 24 hours at a temperature of 25°C.
上述の各試料についてハンダ耐熱性および水中での取り
はずし性について試験を行った。ハンダ耐熱性試験は2
60℃の温度のハンダ槽内に上述の仮固定された各試料
をそれぞれ、3秒間、2回浸漬し、目視により電子部品
3の浮き、ずれなどを観察した。また、取りはずし性に
ついては温度80℃の攪拌温水中に各試料を浸漬して剥
離状態を観察した。結果を表
2に示す。Each of the above samples was tested for solder heat resistance and underwater removability. Solder heat resistance test is 2
Each of the temporarily fixed samples described above was immersed twice for 3 seconds in a solder bath at a temperature of 60° C., and the electronic components 3 were visually observed for lifting, displacement, etc. Moreover, regarding removability, each sample was immersed in stirred warm water at a temperature of 80° C. and the state of peeling was observed. The results are shown in Table 2.
表
表−2から明らかなように、本発明組成物に係る試料N
[L lおよび2はハンダ耐熱性ならびに取りはずし性
の両方とも満足な値を示している。As is clear from Table 2, sample N according to the composition of the present invention
[L l and 2 show satisfactory values for both solder heat resistance and removability.
以上のように、本発明における接着剤組成物は、ハンダ
による本接合時には電子部品のずれ、脱落がなく、また
、水による取りはすしが簡単なため、電子部品交換時の
作業性の向上が期待でき、有機溶剤による洗浄も必要と
しないため、作業環境も良好である。As described above, the adhesive composition of the present invention prevents electronic components from shifting or falling off during main bonding with solder, and can be easily removed with water, improving workability when replacing electronic components. This is promising and does not require cleaning with organic solvents, so the working environment is also good.
第1図は電子部品の取り付は状態を示す平面図、第2図
は第1図の断面図である。
1・・プリント基板、 2・・接着剤
3・・電子部品。FIG. 1 is a plan view showing how electronic parts are mounted, and FIG. 2 is a sectional view of FIG. 1. 1. Printed circuit board, 2. Adhesive 3. Electronic parts.
Claims (3)
該電子部品の仮固定用として使用される接着剤組成物に
おいて、次の成分(A)、(B)、(C)および(D)
を含むことを特徴とする仮固定用接着剤組成物。 (A)分子内に重合可能なエチレン性二重結合を少なく
とも一つ有し、かつ重合物が吸水性または水溶性となり
得るモノマー。 (B)吸水性および/または水溶性高分子物質。 (C)分子内にエチレン性二重結合を少なくとも一つ有
し、かつ重合物が非吸水性または非水溶性となり得るオ
リゴマ−またはプレポリマー。 (D)重合開始剤。(1) In an adhesive composition used for temporarily fixing electronic components before soldering them onto a printed circuit board, the following components (A), (B), (C) and (D) are used.
An adhesive composition for temporary fixing, comprising: (A) A monomer that has at least one polymerizable ethylenic double bond in its molecule and that allows the polymer to be water-absorbing or water-soluble. (B) Water-absorbing and/or water-soluble polymeric substances. (C) An oligomer or prepolymer that has at least one ethylenic double bond in its molecule and can be non-water-absorbing or water-insoluble. (D) Polymerization initiator.
)および(B)の合計使用量100重量部に対し、成分
(C)の使用量が0.1〜25重量部であり、かつ成分
(D)の使用量が0.01〜10重量部である仮固定用
接着剤組成物。(2) In the composition according to claim 1, the component (A
) and (B), the amount of component (C) used is 0.1 to 25 parts by weight, and the amount of component (D) used is 0.01 to 10 parts by weight. An adhesive composition for temporary fixing.
(A)、(B)、(C)および(D)に加えて、さらに
成分(B)として無機充填剤を含むことを特徴とする仮
固定用接着剤組成物。(3) The composition according to claim 1, further comprising an inorganic filler as component (B) in addition to the components (A), (B), (C), and (D). An adhesive composition for temporary fixing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2129456A JP2903333B2 (en) | 1990-05-19 | 1990-05-19 | Adhesive composition for temporary fixing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2129456A JP2903333B2 (en) | 1990-05-19 | 1990-05-19 | Adhesive composition for temporary fixing |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0423875A true JPH0423875A (en) | 1992-01-28 |
JP2903333B2 JP2903333B2 (en) | 1999-06-07 |
Family
ID=15009938
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2129456A Expired - Lifetime JP2903333B2 (en) | 1990-05-19 | 1990-05-19 | Adhesive composition for temporary fixing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2903333B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007004620A1 (en) * | 2005-07-04 | 2007-01-11 | Denki Kagaku Kogyo Kabushiki Kaisha | Curable composition and method for temporal fixation of structural member using the same |
JP2007016141A (en) * | 2005-07-08 | 2007-01-25 | Denki Kagaku Kogyo Kk | Composition and method of temporarily fixing member using the same |
JP2007056066A (en) * | 2005-08-22 | 2007-03-08 | Denki Kagaku Kogyo Kk | Composition and method for temporarily fixing member by using the same |
JP2007186630A (en) * | 2006-01-16 | 2007-07-26 | Denki Kagaku Kogyo Kk | Composition and method for fixing component temporarily using it |
WO2019004431A1 (en) * | 2017-06-29 | 2019-01-03 | 株式会社Adeka | Adhesive composition |
KR20210016745A (en) | 2019-08-05 | 2021-02-17 | 이승주 | Turning direction apparatus of vehicles |
-
1990
- 1990-05-19 JP JP2129456A patent/JP2903333B2/en not_active Expired - Lifetime
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007004620A1 (en) * | 2005-07-04 | 2007-01-11 | Denki Kagaku Kogyo Kabushiki Kaisha | Curable composition and method for temporal fixation of structural member using the same |
US8313604B2 (en) | 2005-07-04 | 2012-11-20 | Denki Kagaku Kogyo Kabushiki Kaisha | Curable composition and temporary fixation method of member using it |
JP2007016141A (en) * | 2005-07-08 | 2007-01-25 | Denki Kagaku Kogyo Kk | Composition and method of temporarily fixing member using the same |
JP4480641B2 (en) * | 2005-07-08 | 2010-06-16 | 電気化学工業株式会社 | Composition and method for temporarily fixing member using the same |
JP2007056066A (en) * | 2005-08-22 | 2007-03-08 | Denki Kagaku Kogyo Kk | Composition and method for temporarily fixing member by using the same |
JP2007186630A (en) * | 2006-01-16 | 2007-07-26 | Denki Kagaku Kogyo Kk | Composition and method for fixing component temporarily using it |
WO2019004431A1 (en) * | 2017-06-29 | 2019-01-03 | 株式会社Adeka | Adhesive composition |
JPWO2019004431A1 (en) * | 2017-06-29 | 2020-04-30 | 株式会社Adeka | Adhesive composition |
KR20210016745A (en) | 2019-08-05 | 2021-02-17 | 이승주 | Turning direction apparatus of vehicles |
Also Published As
Publication number | Publication date |
---|---|
JP2903333B2 (en) | 1999-06-07 |
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