JPS63144891A - Cream solder - Google Patents

Cream solder

Info

Publication number
JPS63144891A
JPS63144891A JP29369086A JP29369086A JPS63144891A JP S63144891 A JPS63144891 A JP S63144891A JP 29369086 A JP29369086 A JP 29369086A JP 29369086 A JP29369086 A JP 29369086A JP S63144891 A JPS63144891 A JP S63144891A
Authority
JP
Japan
Prior art keywords
cream solder
rosin
solder
solvent
propylene oxide
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
Application number
JP29369086A
Other languages
Japanese (ja)
Other versions
JP2520118B2 (en
Inventor
Toshiaki Ogura
小倉 利明
Koichi Hagio
浩一 萩尾
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NIPPON GENMA KK
Original Assignee
NIPPON GENMA KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by NIPPON GENMA KK filed Critical NIPPON GENMA KK
Priority to JP61293690A priority Critical patent/JP2520118B2/en
Publication of JPS63144891A publication Critical patent/JPS63144891A/en
Application granted granted Critical
Publication of JP2520118B2 publication Critical patent/JP2520118B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To obtain cream solder which obviates a change of viscosity, skinning and drying and has good workability by compounding an addition product of 2-ethyhexanol and ethylene oxide an/or propylene oxide as a solvent to the cream solder. CONSTITUTION:The addition product of the 2-ethyhexanol and ethylene oxide an/or propylene oxide is compounded as the solvent with the cream solder. The molar number of the ethylene oxide an/or propylene oxide to be added is preferably set at 1-4. The prepn. of the cream solder is executed by adequately compounding powder solder, rosin, etc., as a flux, activator, etc., with the above-mentioned solvent. The cream solder having such cream characteristics as freedom from the change of viscosity, good workability and good solderability in combination is thereby obtd.

Description

【発明の詳細な説明】 産業上の利用分野 本発明はクリームはんだ、特に溶剤として2−エチルヘ
キサノールと酸化エチレンおよび/または酸化プロピレ
ンとの付加物を配合したクリームはんだに関する。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a cream solder, particularly a cream solder containing an adduct of 2-ethylhexanol and ethylene oxide and/or propylene oxide as a solvent.

従来の技術 クリームはんだは樹脂、活性剤、粘弾性調整剤、添加剤
等を溶剤に溶解分散させて得られるフラックスにはんだ
粉をクリーム状に分散させた乙ので、被接合金属間に塗
布後、加熱融着される。
Conventional technology Cream solder is a flux obtained by dissolving and dispersing resin, activator, viscoelasticity modifier, additives, etc. in a solvent, and solder powder is dispersed in a cream form. Heat fused.

クリームはんだ用溶剤としては、天然ロジンやロジン単
量体等に対して良好な溶解特性を有して安定な溶液を提
供する等の理由からキンレン、ターピネオール、ヘキン
レングリコール等が古くから使用されてきたが、乾燥速
度が非常に早いために塗布後の作業性が悪い、空気酸化
によってはんだボールや残渣が生じやすい、活性剤に対
する溶解性が悪いためにはんだ付性のバラツキや腐食か
発生しやすい等の欠点があった。
As a solvent for cream solder, quinolene, terpineol, hequinlene glycol, etc. have been used for a long time because they have good dissolution characteristics for natural rosin and rosin monomer, and provide a stable solution. However, the drying speed is very fast, resulting in poor workability after application, the tendency to form solder balls and residue due to air oxidation, and the poor solubility of activators, resulting in uneven solderability and corrosion. It had drawbacks such as being easy to use.

その後、溶液安定性の良好な合成ロジンの実用化に伴っ
てジエチレングリコールモノブチルエーテル、エチレン
グリコールモノフェニルエーテル、ノイソブチルアジペ
ート、DOP等の溶剤またはポリブテン類等の不乾燥性
液状粘着性物質が使用されるようになって比較的骨れた
特性を有するクリームはんだが得られるようになっr二
。     ゛しかしながら、ジエチレングリコールモ
ノブチルエーテルは吸湿性が高いのでクリームはんだの
粘度変化が大きくなり、エチレングリコールモノフェニ
ルエーテルは特異臭を有し、ジイソブチルアジペートや
DOP等のエステルは親水性が低いために活性剤との相
溶性が悪い等の問題があり、またポリブテン類等の液状
粘着性物質はロジン系樹脂や活性剤との相溶性が悪いの
で配合量に制限がある。
Subsequently, with the practical use of synthetic rosins with good solution stability, solvents such as diethylene glycol monobutyl ether, ethylene glycol monophenyl ether, noisobutyl adipate, and DOP, or non-drying liquid sticky substances such as polybutenes were used. As a result, cream solder with relatively robust properties has become available. However, diethylene glycol monobutyl ether has high hygroscopicity, which causes a large change in the viscosity of cream solder, ethylene glycol monophenyl ether has a peculiar odor, and esters such as diisobutyl adipate and DOP have low hydrophilicity, so they cannot be used as activators. There are problems such as poor compatibility with rosin resins and activators, and liquid adhesive substances such as polybutenes have poor compatibility with rosin resins and activators, so there is a limit to the amount they can be blended.

発明が解決しようとする問題点 本発明者はこのような事情に鑑み、クリームはんだに要
求される諸特性、即ち、粘度が変化しない、はんだボー
ルや残渣の発生が少ない、皮はりゃ乾燥がなく作業性が
よい、はんだ付性がよい、悪臭や毒性が少ない等の特性
を有するクリームはんだを提供するために鋭意検討を重
ねた結果、2−エチルヘキサノールと酸化エチレンおよ
び/または酸化プロピレンとの付加物を溶剤として使用
することによってこの課題が解決されることを究明して
本発明を完成した。
Problems to be Solved by the Invention In view of the above circumstances, the present inventor has developed a technology that meets the various characteristics required of cream solder, namely, no change in viscosity, little generation of solder balls and residue, and no drying of the skin. As a result of extensive research in order to provide a cream solder with properties such as good workability, good solderability, and low odor and toxicity, we found that the addition of 2-ethylhexanol and ethylene oxide and/or propylene oxide The present invention was completed by discovering that this problem could be solved by using a substance as a solvent.

問題点を解決するための手段 即ち本発明は、2−エチルヘキサノールと酸化エチレン
および/または酸化プロピレンとの付加物を含有するク
リームはんだに関する。
SUMMARY OF THE INVENTION The present invention relates to a cream solder containing an adduct of 2-ethylhexanol and ethylene oxide and/or propylene oxide.

本発明に使用する付加物は常法により、2−エチルヘキ
サノールに酸化エチレンおよび/または酸化プロピレン
を付加さけることによって容易に調製することができる
The adduct used in the present invention can be easily prepared by adding ethylene oxide and/or propylene oxide to 2-ethylhexanol by a conventional method.

酸化エチレンおよび/または酸化プロピレンの付加モル
数は通常1〜4、好ましくは1〜2であり、5以上にな
ると活性剤の溶解性が低下する。
The number of moles of ethylene oxide and/or propylene oxide added is usually 1 to 4, preferably 1 to 2, and when it is 5 or more, the solubility of the active agent decreases.

一般に、2−エチルヘキサノールと酸化プロピレンとの
付加物は2−エチルヘキサノールと酸化エチレンとの付
加物に比べて、沸点は低いが、吸湿性か低くて安定で、
臭いが弱く、毒性も低い等の点で好ましいものであるが
、酸化プロピレンと酸化エチレンの両方を、付加割合お
よび付加順序を適宜変化させることによって2−エチル
ヘキサノールに付加させることによって親水性や沸点等
を適当に調整することができる。
Generally, the adduct of 2-ethylhexanol and propylene oxide has a lower boiling point than the adduct of 2-ethylhexanol and ethylene oxide, but it is less hygroscopic and stable.
Although it is preferable because it has a weak odor and low toxicity, it is possible to improve hydrophilicity and boiling point by adding both propylene oxide and ethylene oxide to 2-ethylhexanol by appropriately changing the addition ratio and order of addition. etc. can be adjusted appropriately.

このような2−エチルヘキサノールと酸化アルキレンと
の付加物は活性水素を有するので、活性剤に対しても良
好な溶剤となるのでこれを安定に含有させて均一なはん
だ付性を保証すると共に被接合金属の腐食を有効に防止
する。
Since such an adduct of 2-ethylhexanol and alkylene oxide has active hydrogen, it becomes a good solvent for the activator, so it is possible to stably contain it to ensure uniform solderability and to reduce the amount of soldering. Effectively prevents corrosion of joining metals.

さらにこのような付加物は、炭素原子数の比較的大きな
アルキル主鎖に側鎖としてエチル基を有するので、ロジ
ン等の樹脂の溶解安定性が極めて良く、粘度変化が少な
いばかりでなく、急速な蒸発乾燥がおこらないので乾燥
によるはんだボールの発生や被接合部品の固着力不足等
の問題は起こらず、また大気中からの水分の混入量が非
常に少ないので、印刷後の放置による吸湿に起因するは
んだボールの発生は極めて少ない。
Furthermore, such adducts have an ethyl group as a side chain on the alkyl main chain with a relatively large number of carbon atoms, so they have extremely good dissolution stability for resins such as rosin, and not only have little viscosity change but also rapid dissolution. Since evaporation drying does not occur, problems such as the formation of solder balls due to drying and insufficient adhesion of parts to be bonded do not occur, and since the amount of moisture mixed in from the atmosphere is extremely small, it is possible to prevent problems such as the formation of solder balls due to drying or insufficient adhesion of parts to be joined. The occurrence of solder balls is extremely rare.

上記のクリームはんだ用溶剤には、前述のクリームはん
だに要請される諸特性を阻害しない範囲内において従来
から常用されている溶剤を所望により適宜配合してもよ
い。
The above-mentioned cream solder solvent may optionally contain conventionally used solvents as long as they do not impede the properties required of the above-mentioned cream solder.

本発明によるクリームはんだには上記の溶剤中に常套の
配合成分即ち、粉末はんた、ロジンまたはロジン誘導体
、活性剤および所望により熱可塑性樹脂類、油脂類(脂
肪酸を含む)、酸化防止剤(例えば、BHT)、増粘剤
、消泡剤、艶消剤等を適宜配合する。
The cream solder according to the invention contains the conventional ingredients in the above-mentioned solvent, namely powdered solder, rosin or rosin derivatives, activators and optionally thermoplastic resins, oils and fats (including fatty acids), antioxidants ( For example, BHT), a thickener, an antifoaming agent, a matting agent, etc. are appropriately blended.

粉末はんだは全クリームハンダの70〜92重量%配合
し、残りは溶剤と他の添加剤、即ち、フラックスである
Powdered solder makes up 70 to 92% by weight of the total cream solder, with the remainder being solvent and other additives, ie, flux.

液状フラックスとしてはロジンまたはロジン誘導体30
〜80重量部、活性剤10〜0重量部、熱可塑性樹脂お
よび油脂類25〜6重量部、溶剤20〜70重量部を基
本成分とし、その他の添加剤を適宜配合すればよい。粘
度は5oooo〜6ooooo程度が好ましい。
Rosin or rosin derivative 30 as liquid flux
The basic components are ~80 parts by weight, 10-0 parts by weight of an activator, 25-6 parts by weight of thermoplastic resin and fats and oils, and 20-70 parts by weight of a solvent, and other additives may be blended as appropriate. The viscosity is preferably about 5oooo to 6ooooo.

本発明に用いるロジンまたはロジン誘導体は従来フラッ
クスに使用されてきたもの、例えばロジン、不均化ロジ
ン、水素添加ロジン、マレイン化ロジン、重合ロジン等
を用いればよい。
The rosin or rosin derivative used in the present invention may be those conventionally used for fluxes, such as rosin, disproportionated rosin, hydrogenated rosin, maleated rosin, and polymerized rosin.

活性剤としては含窒素塩基のハロゲン化水素塩、有機酸
塩、有機酸、アミノ酸等が例示される。含窒素塩基とし
てはアンモニア、第1、第2、第3アミン、芳香族アミ
ン、異項環式アミン、グアニジン、尿素、アミド、アル
カノールアミン、ポリアミン等がある。ハロゲン化水素
としてはHC&。
Examples of the activator include hydrogen halides of nitrogen-containing bases, organic acid salts, organic acids, and amino acids. Examples of nitrogen-containing bases include ammonia, primary, secondary, and tertiary amines, aromatic amines, heterocyclic amines, guanidine, urea, amides, alkanolamines, and polyamines. Hydrogen halides include HC&.

1−IBr、HF等がある。有機酸としては酢酸、乳酸
、フタール酸、マレイン酸、フマール酸、アジピン酸、
アミノ酸としてはグリシン、アラニン、アスパラギン酸
、グルタミン酸等が例示される。
1-IBr, HF, etc. Organic acids include acetic acid, lactic acid, phthalic acid, maleic acid, fumaric acid, adipic acid,
Examples of amino acids include glycine, alanine, aspartic acid, and glutamic acid.

熱可塑性樹脂はフラックスの粘度を調整し、あるいは粘
性、弾性、組成等を改良して、フラックスの塗布特性を
改良するものであり、一般に熱可塑性樹脂および油脂が
使用される。本発明において好適な熱可塑性樹脂は合成
ワックス類、マレイン酸樹脂、ポリスチレン、変性アル
キッド樹脂、エステルガム、ポリブチラール、ポリアミ
ド等であるが前述のマレイン化ロジン、ロジン変性フェ
ノールホルマリン重縮合物、ロジン自体を粘度調整剤と
して用いてもよい。この場合、粘度調整剤として特別の
成分を加える必要はなく、これも本発明の技術的範囲に
包含されるものである。粘度調整剤としてはセラック、
乾性油、部分エステル化フェア′−ル樹脂等を用いても
よい。
The thermoplastic resin adjusts the viscosity of the flux or improves the viscosity, elasticity, composition, etc., and improves the application characteristics of the flux, and generally thermoplastic resins and oils are used. Suitable thermoplastic resins in the present invention include synthetic waxes, maleic acid resins, polystyrene, modified alkyd resins, ester gums, polybutyral, polyamides, etc., including the aforementioned maleated rosin, rosin-modified phenol-formalin polycondensate, and rosin itself. may be used as a viscosity modifier. In this case, there is no need to add a special component as a viscosity modifier, and this is also within the technical scope of the present invention. Shellac as a viscosity modifier,
Drying oils, partially esterified Fair'all resins, etc. may also be used.

このような樹脂は使用する塗装方式に合わせて所望の粘
弾特性が得られるように添加する。この点については従
来のはんだ付において用いられた技術を利用することが
できる。
Such resins are added so as to obtain desired viscoelastic properties depending on the coating method used. In this regard, techniques used in conventional soldering can be utilized.

以下、本発明を実施例によって説明する。Hereinafter, the present invention will be explained by examples.

実施例1 表−1の配合処方により調製したフラックス12重量%
と粉末はんだ(粒度325メツシユ)88重M%とを十
分に混練してクリームはんだAを調製した。
Example 1 12% by weight of flux prepared according to the formulation shown in Table 1
Cream solder A was prepared by sufficiently kneading the powdered solder (particle size: 325 mesh) and 88% by weight M%.

得られたクリームはんだAについて以下の特性を調べ、
結果を表−2に示す。
The following characteristics of the obtained cream solder A were investigated,
The results are shown in Table-2.

(1)活性剤の溶解性:フラックス配合時の活性剤の溶
解性(「○」・良好、「×」:不良)。
(1) Solubility of activator: Solubility of activator when blending flux ("○": good, "×": poor).

(2)塗布直後の残渣・塗布後、直ちにリフローをおこ
なったときの残渣の程度(rOJ:f2、「△」:可、
「X」:不良)。
(2) Residue immediately after application - Level of residue when reflowing immediately after application (rOJ: f2, "△": OK,
"X": defective).

(3)経時後の残渣:塗布後、12時間経過後にリフロ
ーをおこなったときの残渣の程度 (rXj:優、「△」:可、「×」:不良)。
(3) Residue after time: degree of residue when reflow was performed 12 hours after application (rXj: excellent, "△": fair, "×": poor).

(4)はんだ付性二酸化処理銅板に対するはんだ付性(
「○」:優、「△」:可、「×」:不可)。
(4) Solderability Solderability to carbon dioxide treated copper plate (
"○": Excellent, "△": Acceptable, "×": Not acceptable).

(5)臭:リフロ一時に発生する臭気の程度(「O」:
無臭、「△」有臭、「×」:不快臭)。
(5) Odor: Degree of odor generated during reflow (“O”:
Odorless, "△" odor, "x": unpleasant odor).

(6)粘着性;塗布後、すぐに被接合部品を付けた時の
固着力の程度(「○」:f9、「△」:可、「×」:不
可)。
(6) Adhesiveness: degree of adhesion when parts to be joined are attached immediately after application ("○": f9, "△": acceptable, "×": not possible).

(7)皮はり性:塗布後、12時間経過後の皮はりの程
度(「○」:優、「△」:可、「×」:不可)。
(7) Skin elasticity: degree of skin elasticity 12 hours after application ("○": excellent, "△": fair, "x": poor).

(8)樹脂の溶解安定性ニ調製後、100日経過後の樹
脂の溶解分散状態(「○」:安定、「×」:不安定)。
(8) Dissolution stability of the resin Dissolution and dispersion state of the resin 100 days after preparation ("○": stable, "x": unstable).

比較例1〜8 表−1の配合処方により調製したフラックスを用いて実
施例1と同様にしてクリームはんだa−hを調製した。
Comparative Examples 1 to 8 Cream solders a to h were prepared in the same manner as in Example 1 using fluxes prepared according to the formulations shown in Table 1.

得られたクリームはんだa=hについて実施例1と同様
にして、活性剤の溶解性等の特性を調べた。
The properties of the obtained cream solder a=h, such as the solubility of the active agent, were investigated in the same manner as in Example 1.

結果を表−2に示す。The results are shown in Table-2.

発明の効果 本発明によるクリームはんだは、可塑剤の原料等として
高純度かつ低コストで容易に入手可能な2−エチルヘキ
ンルアルコールに酸化エチレンおよび/または酸化プロ
ピレンを付加させた付加物を溶剤として含有することを
特徴とし、粘度の経時変化がない、はんだボールや残渣
の発生が少ない、皮はりゃ乾燥がなくて作業性がよい、
はんだ付性がよい、悪臭や毒性が少ない等、クリームは
んだに要求される諸特性を兼有する。
Effects of the Invention The cream solder according to the present invention uses, as a solvent, an adduct obtained by adding ethylene oxide and/or propylene oxide to 2-ethylhexyl alcohol, which is easily available at high purity and low cost as a raw material for a plasticizer. It is characterized by the fact that the viscosity does not change over time, there is little generation of solder balls and residue, and the skin does not dry out, making it easy to work.
It has all the properties required of cream solder, such as good solderability, low odor and toxicity.

Claims (1)

【特許請求の範囲】 1、2−エチルヘキサノールと酸化エチレンおよび/ま
たは酸化プロピレンとの付加物を含有するクリームはん
だ。 2、酸化エチレンおよび/または酸化プロピレンの付加
モル数が1〜4である第1項記載のクリームはんだ。 3、付加物が2−エチルヘキサノールと酸化プロピレン
との付加物である第1項記載のクリームはんだ。
[Claims] A cream solder containing an adduct of 1,2-ethylhexanol and ethylene oxide and/or propylene oxide. 2. The cream solder according to item 1, wherein the number of moles of ethylene oxide and/or propylene oxide added is 1 to 4. 3. The cream solder according to item 1, wherein the adduct is an adduct of 2-ethylhexanol and propylene oxide.
JP61293690A 1986-12-09 1986-12-09 Cream solder Expired - Lifetime JP2520118B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61293690A JP2520118B2 (en) 1986-12-09 1986-12-09 Cream solder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61293690A JP2520118B2 (en) 1986-12-09 1986-12-09 Cream solder

Publications (2)

Publication Number Publication Date
JPS63144891A true JPS63144891A (en) 1988-06-17
JP2520118B2 JP2520118B2 (en) 1996-07-31

Family

ID=17797970

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61293690A Expired - Lifetime JP2520118B2 (en) 1986-12-09 1986-12-09 Cream solder

Country Status (1)

Country Link
JP (1) JP2520118B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9464305B2 (en) 1996-08-30 2016-10-11 Suntory Holdings Limited Process for producing unsaturated fatty acid-containing oils

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9464305B2 (en) 1996-08-30 2016-10-11 Suntory Holdings Limited Process for producing unsaturated fatty acid-containing oils

Also Published As

Publication number Publication date
JP2520118B2 (en) 1996-07-31

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