JPH0588279B2 - - Google Patents

Info

Publication number
JPH0588279B2
JPH0588279B2 JP60021517A JP2151785A JPH0588279B2 JP H0588279 B2 JPH0588279 B2 JP H0588279B2 JP 60021517 A JP60021517 A JP 60021517A JP 2151785 A JP2151785 A JP 2151785A JP H0588279 B2 JPH0588279 B2 JP H0588279B2
Authority
JP
Japan
Prior art keywords
rosin
adhesive
soldering
adhesive according
acid value
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.)
Expired - Lifetime
Application number
JP60021517A
Other languages
Japanese (ja)
Other versions
JPS61181883A (en
Inventor
Toshiaki Ogura
Hideo Chaki
Koichi Hagio
Noboru Yamazaki
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP60021517A priority Critical patent/JPS61181883A/en
Publication of JPS61181883A publication Critical patent/JPS61181883A/en
Publication of JPH0588279B2 publication Critical patent/JPH0588279B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/30Assembling printed circuits with electric components, e.g. with resistor
    • H05K3/303Surface mounted components, e.g. affixing before soldering, aligning means, spacing means
    • H05K3/305Affixing by adhesive
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product

Landscapes

  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Electric Connection Of Electric Components To Printed Circuits (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明はチツプ部品等の小形部品をクリームは
んだでロウ接する場合に、基板に部品を接着する
事を目的とした接着剤に関する。 基板にクリームはんだを塗布し、チツプ部品を
装置した後、はんだ付が完了するまでの時期にお
いて、部品類の固定を行なうためのはんだ付用一
時接着剤に関する。 従来技術 近年電子基板は、ますます小形化される傾向が
あり、部品の微小化、実装密度の上昇が図られる
に従い、クリームはんだやチツプ部品の使用が増
大している。 通常の電子部品類には部品の固定や配線、はん
だ付を行なうに必要、かつ十分なリード線がある
が、チツプ部品は部品の高密度実装を可能にする
ため部品を固定するに十分なリード線がない。従
つてリードレス部品は基板上に固定する事が難か
しく、基板の移動時や加熱溶融時に位置ずれ等を
おこしやすい。これを防止する為にエポキシ等の
熱硬化性樹脂で部品類を予め接着させておく方法
が提案されているが、この方法でははんだ付部被
接合面に接着剤が付着した場合、はんだ付が不可
能になる。 またワツクス−高級脂肪酸を原料とした組成物
が、部品等を固定するために使用される場合もあ
るが、部品等を確実に接着するために必要な粘着
性に劣り、冷時はもろくて割れやすく、100℃程
度の熱で溶け流動するために、基板の移動時や加
熱溶融時に部品の落下やずれ等がおこりやすく、
洗浄性が劣る。 発明の目的 本発明者らは、十分な接着性、粘着性、弾力性
をもち、かつ、はんだ付の阻害や熱時における流
動が無く、さらに洗浄性の良好な組成物を求めて
種々の検討を行つた結果、本発明を完成した。 本発明は、はんだ付を阻害せず、むしろはんだ
付を促進させる作用をもち、かつはんだ付時の熱
によつて流動することなく、十分な部品接着力を
有し、さらに容易に洗浄できるはんだ付用一時接
着剤を提供する。 発明の構成 本発明はロジン系樹脂、増粘剤、および可塑剤
の混合物を含み、増粘剤が有機ベントナイト、ベ
ントナイト、カオリン、タルク、クレー、超微粉
シリカ、疎水性超微粉シリカ、超微粉アルミナお
よび金属石鹸から選ばれる、酸価20以上を有し、
常温で固体であり、80℃で1000cps以上の粘度を
有するはんだ付用一時接着剤を提供する。 本発明に用いるロジン系樹脂としては、軟化点
60〜140℃の樹脂が適当であり、酸価は有してい
ても有していなくてもよい。酸価を有しないか、
比較的小さい場合は、可塑剤や添加剤として酸価
を有する成分を配合し、最終製品の酸価が20以
上、好ましくは50以上となるようにする。本発明
接着剤が接着性を有すると共に、後のはん付性に
悪影響を与えず、むしろこれに寄与させる上で、
酸価が20以上であるのが特に好ましい。 本発明に用いるロジン系樹脂としては、天然ロ
ジン、水素添加ロジン、不均化ロジン、マレイン
酸変性ロジン、フエノール変性ロジン、重合ロジ
ン、ロジン多価アルコールエステルが好ましく、
特に好ましくは水素添加ロジンである。水素添加
ロジンは水素添加されている事より、耐熱性や耐
酸化性に優れ、非重合性で、良好な洗浄性を示
し、良好な酸価を有する。 本発明に用いる増粘剤は接着剤に適当な粘弾性
を与え、電子部品を接着する際、接着部分から流
れ出ず局部塗布が容易で、接着後は電子部品を固
定する十分な強度を附与するためのものであり、
常温および接着剤の塗布温度で固体の粉末であ
る。粒度は70μm以下、特に40μm以下のものを用
いるのが好ましい。 増粘剤としては高融点有機物微粉末、無機系微
粉末があるが、加熱時の粘度特性の面から無機系
微粉末を用いるのが好ましく、具体的には例え
ば、有機物としては金属石けん、無機物としては
有機ベントナイト、ベントナイト、カオリン、タ
ルク、クレー、超微粉シリカ、疎水性超微粉シリ
カ、超微粉アルミナ等があげられる。特に好まし
くは、有機ベントナイトであり、これははんだ付
性や洗浄性を低下させ難く、粘度調整作用が大き
い。 本発明では所望により可塑剤を配合する。可塑
剤の役割は主として、接着剤の硬さ、溶融時の粘
度調整および接着後の接着部のもろさを解消する
ためのものであるが、さらに、ロジン系樹脂が酸
価を有さないか、或いは十分な酸価を有さない場
合、接着剤に酸価を与えるものである。可塑剤は
ロジン系樹脂をよく溶解するものであつて、常温
で液体のものが好ましい。 本発明の接着剤において使用する可塑剤として
は、一般的な可塑剤やりん酸エステル、酸性リン
酸エステル、脂肪族二塩基酸エステル、フタール
酸エステル、ポリアミド、ポリアルキレングリコ
ール、グリコエーテル等の溶媒も使用可能である
が、加熱時に揮発する成分を含有させる事は不適
当である。これは加熱時に揮発する事より部品類
の位置ずれを引き起こす原因になる事による。ま
た液状樹脂は有機溶媒によく溶解する物質、重合
しない物質、適度な極性をもつ物質である事が好
ましい。 従つて水素添加ロジンのメチルエステル、ハイ
ドロアビエチルアルコール、ダイマー酸が好まし
く、特に好ましくは水素添加ロジンのメチルエス
テルで、本発明に用いる固形樹脂との相溶性は極
めてよく、有機溶媒によく溶け、適度な粘着性を
もち、組成物の特性を形成する上で好ましい特性
を有する。 本発明接着剤には、はんだ付用フラツクスに用
いられる他の適宜の添加剤を配合してもよい。 本発明における各種添加剤としては、例えば酸
化防止剤、はんだ付用活性剤、有機酸、含窒素塩
基、界面活性剤、有機溶媒、腐蝕抑制剤、フロス
ト剤、消泡剤、熱硬化性樹脂、ゴム類等があげら
れる。 酸化防止剤としては、フエノール系、硫黄系、
リン系、錫系、オキシム系、アミン系酸化防止剤
があげられるが、フエノール系が特に好ましく、
特に2,6−ジ−tert−ブチル−p−クレゾール
が有効である。 はんだ付用活性剤としては一般的な含窒素塩基
のハロゲン化水素酸塩が使用でき、例えばシクロ
ヘキシルアミンのハロゲン化水素酸塩(HF、
HCl、HBr、HI)等がある。 有機酸としては、脂肪族カルボン酸、脂肪族ジ
カルボン酸、芳香族カルボン酸、オキシカルボン
酸等が使用できるが、洗浄性の面より、安息香
酸、クロロ安息香酸、サリチル酸が有効である。 含窒素塩基としては、脂肪族アミン、芳香族ア
ミン、アミノ酸、アルカノールアミン、含窒素複
素環式化合物、ポリアミン、アミド、グアニジ
ン、ヒドラジン、オキシム等があげられる。とり
わけシクロヘキサノンオキシムが粘着性、はんだ
付性等の面より有効である。これらを用いるとき
は、接着剤全体のアミン価が10以上、好ましくは
20〜160となるよう配合するのがよい。 界面活性剤としては、非イオン界面活性剤が好
ましく、硫黄を含まないのが望ましい。有機溶媒
としてはアルコール、アルカノールアミン、ポリ
アルコール、グリコエーテル、エステル、ケト
ン、炭化水素等いずれも使用できるが、揮発性の
ものの使用は避ける方がよい。 腐蝕抑制剤としては、ベンゾトリアゾール、オ
クチルアミン、ジシクロヘキシルアミン等の含窒
素系腐蝕抑制剤が好ましいが、これに限定される
ものではない。ベンゾトリアゾールが特に好まし
い。 フロスト作用が必要な場合は、従来技術のフロ
スト剤を適宜添加すればよい。 消泡剤としては、シリコン系が有効で、特に分
子量の大なるものが有効である。 本発明はんだ付用一時接着剤の好適な配合比は
ロジン系樹脂40〜80重量%、特に45〜70重量%、
増粘剤3〜30重量%、特に5〜15重量%、可塑剤
0〜60重量%、特に10〜40重量%、およびその他
の添加剤0〜15重量%、特に0〜4重量%であ
る。フラツクス作用を要しない場合は酸価は必ら
ずしも要しないが、好ましくは20以上、特に50〜
160の酸価を有する。 本発明接着剤は常温で固体であり、はんだ付時
溶融しなければならない。また電子部品を基材に
接着させる際の操作上の要請から80℃で1000cps
以上、特に5000〜12000cpsの粘度を有するのが望
ましい。 発明の効果 本発明の組成物は微小部品を安定に接着し、加
熱によつても流れず、部品を所定状態に固定させ
ておくことができる。また低温においても割れ、
はがれが生じない。さらに接合面に組成物が付着
しても、はんだ付を阻害しない。加えて、はんだ
付性に優れ、洗浄性も良い。 本発明は、接着剤とフラツクスに要請される相
反する特性を満足させるものであり、チツプ部品
等の電子部品を精度よく確実に接合する上で非常
に有効である。 実施例 1 以下の成分を配合し、デイゾルバー等の攪拌機
を用いて、120℃で20分間混練し、均一な組成の
はんだ付用一時接着剤を得た。 処 方 重量部 水素添加ロジン(酸価160) 45 水素添加ロジンのメチルエステル 45 有機ベントナイト 10 得られた接着剤の酸価は75、常温で固体であ
り、80℃での粘度は6000cpsであつた。 この接着剤の接着力、流動性、はんだ付性およ
び洗浄性を以下のごとくして評価した。 はんだ付性 銅板(30mm2×0.3mm)に接着剤100mgを塗布し、
はんだ(錫60/鉛40)0.3gを載せ、250℃で30秒
間加熱し、はんだの広がり状態を観察した(試料
数5) 〇:試料全てについて80%以上広がつた。 △:試料の1部が80%未満。 ×:はんだが玉状となり広がらず。 洗浄性 フツ素溶剤(三井フロロケミカル(株)製:フレオ
ンTES)の沸点で接着剤を洗浄し、その洗浄性
を評価した。 〇:1分以内に完全に洗浄 △:1分以内に一部洗浄 ×:1分以内では殆んど洗浄されず。 接着性 ガラス・エポキシ樹脂基板上に接着剤を用い
5gの分銅を接着し、これを50cmの高さから自然
落下させた(試料数5)。 〇:試料全てにつき分銅がとれなかつたもの △:試料の一部で分銅がとれたもの ×:分銅が接着されないもの 流動性 銅板に接着剤を印刷し、120℃に放置し、接着
剤の流動性を評価した。 〇:全く流れない △:一部流れる ×:完全に流動する。 結果を表−1に示す。 実施例 2 以下の処方を用いる以外、実施例1と同様にし
て接着剤を調製した。 処 方 重量部 水素添加ロジンのメチルエステル 43 水素添加ロジン 43 有機ベントナイト 9 2,6−ジ−tert−ブチル−p−クレゾール 0.5 シクロヘキシルアミンHBr 1.5 モノクロロサリチル酸 0.5 シクロヘキサノンオキシム 0.5 ポリオキシエチレンノニルフエニルエーテル
(EO9モル体) 1 ベンゾトリアゾール 0.5 シリコン消泡剤 0.5 得られた接着剤の酸価は70、アミン価は5であ
つた。80℃における粘度は6200cpsであつた。試
験結果を表−1に示す。 比較例 1〜4 以下の処方に示す以外、実施例1と同様にして
接着剤を得た。 〔比較例1の処方〕 パラフインワツクス 90 ステアリン酸 10 〔比較例2の処方〕 カルナウバワツクス 90 ステアリン酸 10 〔比較例3の処方〕 エチレン−酢酸ビニル共重合体 80 カルナウバワツクス 20 〔比較例4の処方〕 エポキシ系接着剤 【表】
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to an adhesive for bonding small parts such as chip parts to a substrate when soldering them with cream solder. This invention relates to a temporary soldering adhesive for fixing parts after cream solder is applied to a board and chip parts are mounted until soldering is completed. BACKGROUND ART In recent years, electronic boards have tended to become smaller and smaller, and as components have become smaller and their packaging density has increased, the use of cream solder and chip components has increased. Ordinary electronic components have the necessary and sufficient lead wires to secure, wire, and solder the components, but chip components require sufficient leads to secure the components in order to enable high-density mounting of components. There are no lines. Therefore, it is difficult to fix leadless components on a substrate, and they are likely to be misaligned when the substrate is moved or heated and melted. In order to prevent this, a method has been proposed in which parts are bonded in advance with thermosetting resin such as epoxy, but with this method, if the adhesive adheres to the surface to be soldered, the soldering will be interrupted. becomes impossible. Also, wax - a composition made from higher fatty acids is sometimes used to fix parts, etc., but it lacks the adhesiveness necessary to reliably bond parts, etc., and is brittle and cracks when cold. Because it melts and flows with heat of about 100℃, parts can easily fall or shift when the board is moved or heated and melted.
Cleanability is poor. Purpose of the Invention The present inventors have conducted various studies in search of a composition that has sufficient adhesion, tackiness, and elasticity, does not inhibit soldering or flow when heated, and has good cleaning properties. As a result, the present invention was completed. The present invention is a solder that does not inhibit soldering but rather promotes soldering, does not flow due to heat during soldering, has sufficient component adhesive strength, and can be easily cleaned. Provide temporary adhesive for attachment. Structure of the Invention The present invention includes a mixture of a rosin resin, a thickener, and a plasticizer, and the thickener is organic bentonite, bentonite, kaolin, talc, clay, ultrafine silica, hydrophobic ultrafine silica, and ultrafine alumina. and metal soap, with an acid value of 20 or more,
Provides a temporary soldering adhesive that is solid at room temperature and has a viscosity of 1000 cps or more at 80°C. The rosin resin used in the present invention has a softening point
A resin having a temperature of 60 to 140°C is suitable, and may or may not have an acid value. Does not have an acid value or
If it is relatively small, components with an acid value are added as plasticizers and additives so that the final product has an acid value of 20 or more, preferably 50 or more. The adhesive of the present invention has adhesive properties and does not adversely affect later soldering properties, but rather contributes to it,
It is particularly preferable that the acid value is 20 or more. As the rosin resin used in the present invention, natural rosin, hydrogenated rosin, disproportionated rosin, maleic acid-modified rosin, phenol-modified rosin, polymerized rosin, and rosin polyhydric alcohol ester are preferable.
Particularly preferred is hydrogenated rosin. Since hydrogenated rosin is hydrogenated, it has excellent heat resistance and oxidation resistance, is non-polymerizable, exhibits good detergency, and has a good acid value. The thickener used in the present invention imparts appropriate viscoelasticity to the adhesive, so that when bonding electronic components, it does not flow out from the bonded area, making it easy to apply locally, and provides sufficient strength to fix the electronic components after bonding. It is for the purpose of
It is a solid powder at room temperature and adhesive application temperature. It is preferable to use particles with a particle size of 70 μm or less, particularly 40 μm or less. Thickeners include high melting point organic fine powders and inorganic fine powders, but it is preferable to use inorganic fine powders from the viewpoint of viscosity properties during heating. Examples include organic bentonite, bentonite, kaolin, talc, clay, ultrafine silica, hydrophobic ultrafine silica, and ultrafine alumina. Particularly preferred is organic bentonite, which does not easily deteriorate solderability or cleanability and has a large viscosity adjusting effect. In the present invention, a plasticizer may be added if desired. The role of the plasticizer is mainly to adjust the hardness of the adhesive, adjust the viscosity during melting, and eliminate the brittleness of the bonded part after bonding. Alternatively, if the adhesive does not have a sufficient acid value, it gives the adhesive an acid value. The plasticizer is preferably one that dissolves the rosin resin well and is liquid at room temperature. Plasticizers used in the adhesive of the present invention include general plasticizers and solvents such as phosphate esters, acidic phosphate esters, aliphatic dibasic acid esters, phthalate esters, polyamides, polyalkylene glycols, and glycoethers. However, it is inappropriate to include components that evaporate during heating. This is because it evaporates during heating and causes misalignment of parts. Further, the liquid resin is preferably a substance that dissolves well in organic solvents, does not polymerize, and has appropriate polarity. Therefore, methyl ester of hydrogenated rosin, hydroabiethyl alcohol, and dimer acid are preferred, and methyl ester of hydrogenated rosin is particularly preferred, as it has extremely good compatibility with the solid resin used in the present invention, dissolves well in organic solvents, It has moderate adhesiveness and has desirable properties in forming the properties of the composition. The adhesive of the present invention may contain other suitable additives used in soldering fluxes. Various additives in the present invention include, for example, antioxidants, soldering activators, organic acids, nitrogen-containing bases, surfactants, organic solvents, corrosion inhibitors, frosting agents, antifoaming agents, thermosetting resins, Examples include rubber. As antioxidants, phenol type, sulfur type,
Examples include phosphorus-based, tin-based, oxime-based, and amine-based antioxidants, but phenol-based antioxidants are particularly preferred;
Particularly effective is 2,6-di-tert-butyl-p-cresol. Typical nitrogen-containing base hydrohalides can be used as soldering activators, such as cyclohexylamine hydrohalides (HF,
HCl, HBr, HI), etc. As the organic acid, aliphatic carboxylic acids, aliphatic dicarboxylic acids, aromatic carboxylic acids, oxycarboxylic acids, etc. can be used, but benzoic acid, chlorobenzoic acid, and salicylic acid are effective from the viewpoint of cleaning properties. Examples of nitrogen-containing bases include aliphatic amines, aromatic amines, amino acids, alkanolamines, nitrogen-containing heterocyclic compounds, polyamines, amides, guanidine, hydrazine, oximes, and the like. In particular, cyclohexanone oxime is more effective in terms of adhesiveness and solderability. When using these, the amine value of the entire adhesive is 10 or more, preferably
It is best to mix it so that it becomes 20-160. The surfactant is preferably a nonionic surfactant, and preferably does not contain sulfur. Alcohols, alkanolamines, polyalcohols, glycoethers, esters, ketones, hydrocarbons, and the like can be used as organic solvents, but it is better to avoid using volatile ones. The corrosion inhibitor is preferably a nitrogen-containing corrosion inhibitor such as benzotriazole, octylamine, dicyclohexylamine, but is not limited thereto. Particularly preferred is benzotriazole. If a frosting effect is required, a conventional frosting agent may be appropriately added. As antifoaming agents, silicone-based antifoaming agents are effective, and those with large molecular weights are particularly effective. The preferred compounding ratio of the temporary soldering adhesive of the present invention is 40 to 80% by weight of rosin resin, particularly 45 to 70% by weight,
3 to 30% by weight of thickeners, especially 5 to 15% by weight, plasticizers 0 to 60% by weight, especially 10 to 40% by weight, and 0 to 15% by weight of other additives, especially 0 to 4% by weight. . If flux action is not required, an acid value is not necessarily required, but it is preferably 20 or higher, especially 50 to 50.
It has an acid value of 160. The adhesive of the present invention is solid at room temperature and must be melted during soldering. In addition, due to operational requirements when bonding electronic components to base materials, the temperature is 1000 cps at 80℃.
Above all, it is particularly desirable to have a viscosity of 5,000 to 12,000 cps. Effects of the Invention The composition of the present invention stably adheres micro parts, does not flow even when heated, and can keep the parts fixed in a predetermined state. It also cracks at low temperatures,
No peeling occurs. Furthermore, even if the composition adheres to the joint surface, it does not inhibit soldering. In addition, it has excellent solderability and is easy to clean. The present invention satisfies the conflicting characteristics required of adhesives and fluxes, and is very effective in accurately and reliably joining electronic components such as chip components. Example 1 The following components were blended and kneaded at 120° C. for 20 minutes using a stirrer such as a dissolver to obtain a temporary soldering adhesive with a uniform composition. Formula Parts by weight Hydrogenated rosin (acid value 160) 45 Methyl ester of hydrogenated rosin 45 Organic bentonite 10 The obtained adhesive had an acid value of 75, was solid at room temperature, and had a viscosity of 6000 cps at 80°C. . The adhesive force, fluidity, solderability, and cleanability of this adhesive were evaluated as follows. Solderability Apply 100mg of adhesive to a copper plate (30mm 2 × 0.3mm),
0.3 g of solder (tin 60/lead 40) was placed on it, heated at 250°C for 30 seconds, and the spread of the solder was observed (number of samples: 5). ○: More than 80% spread for all samples. △: Less than 80% in one part of the sample. ×: Solder becomes beads and does not spread. Cleanability The adhesive was cleaned with the boiling point of a fluorine solvent (Mitsui Fluorochemical Co., Ltd.: Freon TES), and its cleanability was evaluated. ○: Completely washed within 1 minute △: Partially washed within 1 minute ×: Hardly washed within 1 minute. Adhesiveness: Adhesive is used on glass/epoxy resin substrate.
A weight of 5 g was glued and allowed to fall naturally from a height of 50 cm (number of samples: 5). 〇: Weights could not be removed from all samples △: Weights were removed from some of the samples ×: Weights were not attached Fluidity Adhesive was printed on a copper plate, left at 120℃, and the adhesive flowed The gender was evaluated. 〇: No flow at all △: Partial flow ×: Complete flow. The results are shown in Table-1. Example 2 An adhesive was prepared in the same manner as in Example 1 except that the following formulation was used. Formula Parts by weight Methyl ester of hydrogenated rosin 43 Hydrogenated rosin 43 Organic bentonite 9 2,6-di-tert-butyl-p-cresol 0.5 Cyclohexylamine HBr 1.5 Monochlorosalicylic acid 0.5 Cyclohexanone oxime 0.5 Polyoxyethylene nonyl phenyl ether ( 9 mol of EO) 1 Benzotriazole 0.5 Silicone antifoaming agent 0.5 The acid value of the obtained adhesive was 70 and the amine value was 5. The viscosity at 80°C was 6200 cps. The test results are shown in Table-1. Comparative Examples 1 to 4 Adhesives were obtained in the same manner as in Example 1 except for the following formulations. [Formulation of Comparative Example 1] Parafine wax 90 Stearic acid 10 [Formulation of Comparative Example 2] Carnauba wax 90 Stearic acid 10 [Formulation of Comparative Example 3] Ethylene-vinyl acetate copolymer 80 Carnauba wax 20 [ Prescription of Comparative Example 4] Epoxy adhesive [Table]

Claims (1)

【特許請求の範囲】 1 ロジン系樹脂、増粘剤、および可塑剤を含
み、前記増粘剤が有機ベントナイト、ベントナイ
ト、カオリン、タルク、クレー、超微粉シリカ、
疎水性超微粉シリカ、超微粉アルミナおよび金属
石鹸から選ばれる、酸価20以上、常温で固体、80
℃で1000cps以上の粘度を有するはんだ付用一時
接着剤。 2 ロジン系樹脂が軟化点60〜140℃の樹脂であ
る特許請求の範囲第1項記載の接着剤。 3 ロジン系樹脂が天然ロジン、水素添加ロジ
ン、不均化ロジン、マレイン酸変性ロジン、フエ
ノール変性ロジン、重合ロジン、ロジン多価アル
コールエステルから選ばれた特許請求の範囲第1
項記載の接着剤。 4 ロジン系樹脂が酸価10以上を有する特許請求
の範囲第1項記載の接着剤。 5 可塑剤が水素添加ロジンのメチルエステル、
ハイドロアビエチルアルコール、ダイマー酸から
選ばれた特許請求の範囲第1項記載の接着剤。 6 アミン価として10以上のはんだ付用活性剤を
含有する特許請求の範囲第1項記載の接着剤。 7 酸価が50以上である特許請求の範囲第1項記
載の接着剤。
[Claims] 1 Contains a rosin resin, a thickener, and a plasticizer, and the thickener is organic bentonite, bentonite, kaolin, talc, clay, ultrafine silica,
Selected from hydrophobic ultrafine silica, ultrafine alumina, and metal soap, acid value 20 or higher, solid at room temperature, 80
Temporary soldering adhesive with a viscosity of 1000 cps or more at °C. 2. The adhesive according to claim 1, wherein the rosin resin has a softening point of 60 to 140°C. 3. Claim 1 in which the rosin resin is selected from natural rosin, hydrogenated rosin, disproportionated rosin, maleic acid-modified rosin, phenol-modified rosin, polymerized rosin, and rosin polyhydric alcohol ester.
Adhesives listed in section. 4. The adhesive according to claim 1, wherein the rosin resin has an acid value of 10 or more. 5 Plasticizer is hydrogenated rosin methyl ester,
The adhesive according to claim 1, which is selected from hydroabiethyl alcohol and dimer acid. 6. The adhesive according to claim 1, which contains a soldering activator having an amine value of 10 or more. 7. The adhesive according to claim 1, which has an acid value of 50 or more.
JP60021517A 1985-02-05 1985-02-05 Temporary adhesive for soldering Granted JPS61181883A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60021517A JPS61181883A (en) 1985-02-05 1985-02-05 Temporary adhesive for soldering

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60021517A JPS61181883A (en) 1985-02-05 1985-02-05 Temporary adhesive for soldering

Publications (2)

Publication Number Publication Date
JPS61181883A JPS61181883A (en) 1986-08-14
JPH0588279B2 true JPH0588279B2 (en) 1993-12-21

Family

ID=12057156

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60021517A Granted JPS61181883A (en) 1985-02-05 1985-02-05 Temporary adhesive for soldering

Country Status (1)

Country Link
JP (1) JPS61181883A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2525182B2 (en) * 1987-05-22 1996-08-14 内橋エステツク株式会社 How to fix chip type electronic components
JPH0726087B2 (en) * 1989-12-29 1995-03-22 日化精工株式会社 Wafer temporary adhesive and its cleaning agent
JPH0929486A (en) * 1995-07-24 1997-02-04 Matsushita Electric Ind Co Ltd Cream solder
JP4492893B2 (en) * 1999-03-17 2010-06-30 株式会社Dnpファインケミカル Liquid temporary adhesive

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5118245A (en) * 1974-08-05 1976-02-13 Tamura Kaken Co Ltd TSUYAKE SHIFURA TSUKUSU

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5118245A (en) * 1974-08-05 1976-02-13 Tamura Kaken Co Ltd TSUYAKE SHIFURA TSUKUSU

Also Published As

Publication number Publication date
JPS61181883A (en) 1986-08-14

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