Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPH0239357B2 - - Google Patents
[go: Go Back, main page]

JPH0239357B2 - - Google Patents

Info

Publication number
JPH0239357B2
JPH0239357B2 JP59048437A JP4843784A JPH0239357B2 JP H0239357 B2 JPH0239357 B2 JP H0239357B2 JP 59048437 A JP59048437 A JP 59048437A JP 4843784 A JP4843784 A JP 4843784A JP H0239357 B2 JPH0239357 B2 JP H0239357B2
Authority
JP
Japan
Prior art keywords
flux
welding
slag
bulk density
sieve
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
JP59048437A
Other languages
Japanese (ja)
Other versions
JPS60191692A (en
Inventor
Isao Sugioka
Hajime Motosugi
Osami Shimoyama
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 Steel Corp
Original Assignee
Nippon Steel Corp
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 Steel Corp filed Critical Nippon Steel Corp
Priority to JP4843784A priority Critical patent/JPS60191692A/en
Publication of JPS60191692A publication Critical patent/JPS60191692A/en
Publication of JPH0239357B2 publication Critical patent/JPH0239357B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/36Selection of non-metallic compositions, e.g. coatings or fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
    • B23K35/3601Selection of non-metallic compositions, e.g. coatings or fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest with inorganic compounds as principal constituents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Nonmetallic Welding Materials (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は、軟鋼、50HT鋼の薄鋼板の高速溶
接、両側一層溶接、すみ肉溶接、その他表面硬化
肉盛溶接等の潜弧溶接用溶融型フラツクスに関す
るものである。 (従来技術) 高MnO−SiO2系潜弧溶接用溶融型フラツクス
の溶接作業性の改善策としては、特公昭51−
46653号公報に示される如く、発泡させ、多孔質
の粒子とする方法、または特公昭55−42671号公
報に示される如く、フラツクス組成に酸化鉛を加
える方法、がある。 しかし、フラツクス粒子を発泡させ、多孔質と
した粒子のフラツクスでは特開昭51−13340号公
報に示される如く、多孔質であるがゆえに実質表
面積が大きく、付着水分、結晶水等、水分を多く
含み、この水分が溶接によつてガス化し、溶接欠
陥の原因となることが知られている。一方、特公
昭51−46653号公報に示される如く、溶接作業性
能は明らかにかさ密度が小さいフラツクスが良い
ことが知られている。したがつて、多孔質粒子を
含まない、しかも、かさ密度の小さいフラツクス
が提供できれば、溶接作業能率は大いに向上する
ことが期待される。そこで、本発明者らは、特開
昭54−42339号公報で、発泡粒子を含まず、かさ
密度が1.3〜1.55g/cm3の高MnO−SiO2系潜弧溶
接用フラツクスを提案した。このフラツクスを粒
度12×150メツシユとして実際に使用したところ、
フラツクス製造チヤージ間に溶接作業性能のバラ
ツキが発生し、なお、改善の必要のあることが判
明した。 (発明の目的) 本発明は、ビード外観が良好で、溶接欠陥の発
生がなく、スラグ剥離が良く、良好な溶接作業性
能が安定して得られることによつて、溶接作業能
率の向上が計れる、潜弧溶接用溶融型フラツクス
の提供を目的とするものである。 (発明の技術的背景) 前述の、フラツクス製造チヤージ間の溶接作業
性能のバラツキ発生原因として、フラツクス成
分とフラツクスの粒度構成とかさ密度のバラツ
キによつて発生する事が考えられた。そこで、本
発明者らは、フラツクス成分について、特開昭
54−42339号公報に示す成分の見直しを行なつた。 また、フラツクスの粒度構成とかさ密度につ
いては、製造チヤージ間の溶接作業性能の異なる
フラツクスの粒度構成、かさ密度を比較調査した
結果、かさ密度が1.3〜1.55g/cm3の規格範囲内
で、しかも粒度構成がTylerNo.12メツシユのふる
いを通過し、150メツシユのふるいを通過しない
フラツクス製品規格内においても、溶接作業性能
にバラツキのあることが判つた。そこで、フラツ
クス粒度構成を、さらに細かく分類し、JIS規格、
標準ふるいを用いて、比較的粗粒フラツクス粒子
の含有量とかさ密度との間係によるフラツクスの
溶接性能を調査した。 すなわち、フラツクス組成がSiO2とMnOをほ
ぼ同量で計約80%、CaF2を約3%、MgOを約4
%、Bi2O3またはPbOの少なくとも一方を少量添
加した高MnO−SiO2系、試作フラツクスの粒子
を目開き、1410μmのふるいを通過し、149μmの
ふるいを通過しない粒子含有量を90%以上とした
後、さらに、目開き850μmのふるいを通過しな
い比較的粗粒粒子含有量とフラツクスのかさ密度
を変えて、試作フラツクスの溶接性能を調べた。
その結果、第1図に示す如く、かさ密度が同じ場
合でも、目開き850μmのふるいを通過しないフ
ラツクス粒含有量が少ない場合、溶接性能が悪
く、また、目開き850μmのふるいを通過しない
フラツクス含有量は同量でも、かさ密度が大きい
場合、溶接性能が悪い事が判つた。すなわち、目
開き850μmのふるいを通過しないフラツクス粒
子含有量とかさ密度がフラツクスの溶接性能に関
係することが判つた。 なお、第1図中の〇印は、溶接性能が良好であ
ることを示し、×印はスラグ剥離性能、ビード外
観性能のうちいずれか一方、または両方が悪い事
を示す。また、かさ密度の測定は、JIS.K−6721
に準じて測定し、粒度分布の測定は、JIS.Z−
8801に示される網ふるいを用い、ロータツプ式粒
度分布測定機に5分間かけ測定した。 (発明の構成) 本発明の要旨は、「成分が、重量パーセントで
SiO2+MnO:70〜90%、MnO:38%以上、
MnO/SiO2:0.8〜1.3%、MgO:3〜7%、
CaF2:1.5〜4.5%、PbOまたはBi2O3の少なくと
も一方を0.005〜0.5%、CaO:5.0%以下、Na2O
+K2O:0.75%以下、を含有した高MnO−SiO2
系溶融型フラツクスにおいて、その粒度構成が、
目開き1410μmのふるいを通過し、149μmを通過
しないフラツクス粒を90重量%以上含有し、その
内、目開き850μmのふるいを通過しないフラツ
クス粒の含有重量%Aとフラツクスのかさ密度B
との関係が、 1.40≦B≦1.70−1/A−20(ただしA>20とす る。)で表わされる潜弧溶接用溶融型フラツクス」
にある。なお、本発明における%は、重量%の意
味である。 以下に本発明におけるフラツクス成分の含有
量、成分比、などの数値の限定理由、およびかさ
密度、粒度などの数値の限定とそれらの関係式の
限定理由について述べる。 SiO2+MnO:70〜90%、MnO:38%以上、
MnO/SiO2:0.8〜1.3%、とすること; 軟鋼、およびHT50鋼の溶接では、溶接作業性
能を主に考えられたフラツクスが用いられ、従来
から高MnO−高SiO2系のフラツクスが用いられ
て来た。これらは、概ねSiO2+MnO成分が70〜
90%であつた。 また、すみ肉溶接では、MnO成分が38%に満
たない場合、脱酸不足となりやすく、ピツトやブ
ローホールが発生しやすかつた。一方、MnO/
SiO2比は、スラグの融点および剥離性に関し、
0.8に満たないSiO2多量の場合、スラグの融点が
高くなり過ぎる結果、アンダーカツトが発生しや
すく、1.3を超え、MnOが多いかまたはSiO2が少
ない場合、スラグ剥離性が劣化した。 MgO:3〜7%とすること; MgO成分は、3%以上含有することにより、
スラグ剥離性が良くなつた。しかし、7%を超え
て含有すると、溶融スラグの粘性が高くなり過ぎ
る結果、アークが不安定となり、アンダーカツト
が発生しやすく、ビード形状も凸形となり、ビー
ド外観が悪化した。 CaF2:1.5〜4.5%とすること; CaF2成分は、溶接によつて分解し、弗素ガス
を発生し、ピツト、ブローホール等の発生を防止
するシールドガス発生成分として必要な成分であ
り、1.5%未満ではシールドガスの発生が不足し、
4.5%を超えて含有した場合、スラグがビード表
面に焼付きやすくなりスラグ剥離性が劣化した。 PbOまたはBi2O3の少なくとも一方を0.005〜0.5
%とすること; PbOやBi2O3の低融点金属酸化物は、スラグ剥
離性を良くするMgO成分の効果を補助する効果
があつた。スラグ剥離性はMgO成分を増加する
に従い良くなる傾向があつたが、MgO成分の増
加とともにスラグの粘性も高くなる傾向があつ
た。しかし、PbOやBi2O3の少なくとも一方を
0.005%以上添加すればスラグの粘性を下げると
ともにスラグ−メタル間の界面活力を上げ、
MgO成分による剥離性の効果を助けた。この効
果はPbOあるいはBi2O3を単独に添加しても、あ
るいは両方で0.005%以上となるように添加して
も、効果は同じであつた。しかし、0.005%未満
ではその効果は少なく、0.5%を超えて含有した
場合、スラグの粘性が下がり過ぎ、耐湯流れ性が
劣化することによつてビード波形が乱れ、外観が
悪化した。この外観の悪化はPbOあるいはBi2O3
成分を単独で0.5%を超えて添加した場合でも、
両方で0.5%を超えて添加した場合でも同じであ
つた。 CaO:5.0%以下、とすること; CaO成分は、5.0%を超えてフラツクス中に含
有すると、スラグがビード表面に焼付きやすく、
剥離性が悪化した。 Na2O+K2O;0.75%以下、とすること; Na2O、K2O成分は、SiO2やMnO原料鉱石中に
不純物として含まれ、フラツクス中に増加するに
従いスラグ剥離性能、ビード外観、共に悪化する
傾向にあつた。Na2O+K2Oが0.75%を超えて、
フラツクス中に含まれた場合、アーク強さが弱く
なり、アークが不安定になるため、ビードの波目
が乱れ、スラグのかみ込みをおこすことにより、
ビード外観の悪化とともにスラグ剥離性も悪化す
ることが判つた。前述の如くNa2O+K2O成分
は、その含有量が少ないほどビード外観、スラグ
剥離性とも良くなる傾向を示した。 以上の組成範囲内にある高MnO−SiO2系フラ
ツクスにあつても、フラツクス粒子が発泡し、多
孔質化したフラツクスでは、連続的に上層に溶接
される肉盛溶接や、150℃程度以上に予熱された
鋼板のすみ肉溶接を行なう場合、スラグ剥離性能
が悪かつた。 フラツクス粒度構成が、目開き1410μmのふる
いを通過し、149μmを通過しないフラツクス粒
を90重量%以上含有し、その内、目開き850μm、
のふるいを通過しないフラツクス粒の含有重量%
Aとフラツクスのかさ密度Bとの関係が、1.40≦
B≦1.70−1/A−20(ただしA>20とする)であ ること; 本発明のフラツクスは、原材料鉱石を成分目標
に従い混合、溶解した後、ジエツト水流中に投入
し水砕して製造する。従つて、そのフラツクス粒
は、針状又は鹿角状又は球状、あるいは鱗片状の
混在した粒子となることによつて、粗充填法によ
るかさ密度を小さくすることができ、粒子表面積
は、同一かさ密度の発泡粒子に比べ、格段に少な
くなることによつて、粒子表面の付着水分を少な
くし、溶接欠陥の発生を防止することができる。
そのため、同一粒子形状であつても、細粒がフラ
ツクス中に多量に含まれた場合、フラツクスの実
質表面積が大きくなる結果、溶接欠陥の発生が防
止されないこととなる。そこで、溶接欠陥の発生
しない粗粒粒子を多く含むフラツクスであること
が必要となる。目開き、1410μmのふるいを通過
しないフラツクスを多量に含むことは、フラツク
スのシールド効果を低下させるため、溶接欠陥を
起し易く、また、目開き149μmのふるいを通過
する粒子を多く含むフラツクスでは、溶接によつ
て発生した付着水分等のガス化した気体の通気性
が悪化し、ポツクマーク等の欠陥が発生するた
め、粗粒過ぎる粒子と細粒過ぎる粒子は、10%未
満の含有が溶接性能上良好であつた。しかし、本
発明者らは、旧来の粒子形状と異なる針状、鹿角
状、球状あるいは鱗片状粒子の混合体であるフラ
ツクス粒においては、粗充填法によるかさ密度の
測定と粗粒、細粒を除いた粒度の測定のみでは問
題があると考え、粗粒、細粒を除いた粒度構成フ
ラツクスの内、比較的粗粒粒子である、目開き
850μmのふるいを通過しない粒子含有量と粗充
填のかさ密度との関係について、試作フラツクス
の溶接性能を調べた。その結果、溶接性能の良好
なフラツクスのかさ密度は、1.40g/cm3以上、
1.70g/cm3未満であり、比較的粗粒である目開き
850μmのふるいを通過しない粒子含有量は、20
%を越えて必要であつた。しかし、フラツクス全
体のかさ密度が小さい場合、比較的粗粒粒子は、
比較的少量でも溶接性能が良好であつたが、かさ
密度が比較的大きい場合、良好な溶接性能を得る
ためには、目開き850μmのふるいを通過しない、
比較的粗粒のフラツクス粒子が比較的、多量に必
要であつた。 (実施例) 以下に実施例により、本発明の効果を述べる。
第3表に示す成分組成、粒度構成のフラツクスを
試作製造し、第1表に示す鋼板を第2図の如く組
立てたすみ肉溶接試験片に第1表に示すワイヤを
用い、第2表の溶接条件で、試験片を150℃に予
熱した後、下向すみ肉溶接を行ない、それぞれの
フラツクスのスラグ剥離性能とビード外観を調査
した。
(Field of Industrial Application) The present invention relates to a melting type flux for submerged arc welding such as high-speed welding of thin steel plates such as mild steel and 50HT steel, single-layer welding on both sides, fillet welding, and other surface hardening welding. (Prior art) As a measure to improve the welding workability of high MnO-SiO 2 type flux for submerged arc welding,
There is a method of foaming to form porous particles as shown in Japanese Patent Publication No. 46653, and a method of adding lead oxide to the flux composition as shown in Japanese Patent Publication No. 55-42671. However, as shown in Japanese Unexamined Patent Application Publication No. 13340/1983, flux made of particles made porous by foaming them has a large substantial surface area due to its porous nature, and contains a large amount of moisture such as adhering moisture and crystallization water. It is known that this moisture gasifies during welding and causes welding defects. On the other hand, as shown in Japanese Patent Publication No. 51-46653, it is known that a flux with a clearly lower bulk density has better welding performance. Therefore, if a flux that does not contain porous particles and has a low bulk density can be provided, it is expected that welding efficiency will be greatly improved. Therefore, the present inventors proposed a high MnO--SiO 2 -based submerged arc welding flux that does not contain foamed particles and has a bulk density of 1.3 to 1.55 g/cm 3 in Japanese Patent Application Laid-Open No. 54-42339. When this flux was actually used as a mesh of particle size 12 x 150,
It was found that there were variations in welding performance between flux production charges, and that improvements were needed. (Objective of the invention) The present invention improves welding efficiency by providing a good bead appearance, no welding defects, good slag removal, and stable welding performance. The purpose of the present invention is to provide a molten flux for submerged arc welding. (Technical Background of the Invention) The above-mentioned variation in welding performance between flux manufacturing charges was thought to be caused by variation in flux components, flux particle size structure, and bulk density. Therefore, the present inventors investigated the flux components in Japanese Patent Application Laid-open No.
The components shown in Publication No. 54-42339 were reviewed. Regarding the particle size structure and bulk density of flux, as a result of a comparative investigation of the particle size structure and bulk density of fluxes with different welding performance between manufacturing charges, it was found that the bulk density was within the standard range of 1.3 to 1.55 g/cm 3 . Furthermore, it was found that there were variations in welding performance even within the product specifications for fluxes whose particle size structure passed through a Tyler No. 12 mesh sieve but did not pass through a 150 mesh sieve. Therefore, we further classified the flux particle size composition into JIS standards,
Using a standard sieve, we investigated the welding performance of flux depending on the relationship between the content of relatively coarse flux particles and bulk density. In other words, the flux composition is approximately equal amounts of SiO 2 and MnO, totaling approximately 80%, CaF 2 approximately 3%, and MgO approximately 4%.
%, high MnO-SiO 2 system with a small amount of at least one of Bi 2 O 3 or PbO added, the particles of the prototype flux were opened, and the particle content that passed through a 1410 μm sieve and did not pass through a 149 μm sieve was determined to be 90% or more. After that, the welding performance of the prototype flux was investigated by changing the content of relatively coarse particles that do not pass through a sieve with an opening of 850 μm and the bulk density of the flux.
As a result, as shown in Fig. 1, even if the bulk density is the same, if the content of flux grains that do not pass through a sieve with an 850 μm opening is small, welding performance will be poor, and if the content of flux particles that does not pass through a sieve with an 850 μm opening is low, welding performance will be poor. It was found that even if the amount was the same, when the bulk density was large, the welding performance was poor. That is, it was found that the content of flux particles that do not pass through a sieve with an opening of 850 μm and the bulk density are related to the welding performance of the flux. In addition, the mark ◯ in FIG. 1 indicates that the welding performance is good, and the mark x indicates that either one or both of the slag peeling performance and bead appearance performance is poor. In addition, the measurement of bulk density is based on JIS.K-6721.
Particle size distribution measurement is based on JIS.Z-
Using a mesh sieve shown in No. 8801, the measurement was performed using a rotary tap type particle size distribution analyzer for 5 minutes. (Structure of the Invention) The gist of the present invention is that "the components are
SiO 2 + MnO: 70-90%, MnO: 38% or more,
MnO/ SiO2 : 0.8-1.3%, MgO: 3-7%,
CaF2 : 1.5-4.5%, at least one of PbO or Bi2O3 0.005-0.5%, CaO: 5.0% or less , Na2O
High MnO−SiO 2 containing +K 2 O: 0.75% or less
In the system melt type flux, its particle size composition is
Contains 90% by weight or more of flux grains that pass through a sieve with an opening of 1410 μm but do not pass through a sieve with an opening of 850 μm, and the content of flux grains that do not pass through a sieve with an opening of 850 μm A and the bulk density of the flux B
Melting flux for submerged arc welding whose relationship is 1.40≦B≦1.70-1/A-20 (where A>20).
It is in. Note that % in the present invention means % by weight. Below, reasons for limiting numerical values such as content of flux components and component ratios in the present invention, and limiting numerical values such as bulk density and particle size, and reasons for limiting the relational expressions thereof will be described. SiO 2 + MnO: 70-90%, MnO: 38% or more,
MnO/SiO 2 : 0.8 to 1.3%; For welding mild steel and HT50 steel, fluxes mainly designed for welding performance are used, and conventionally high MnO-high SiO 2 fluxes have been used. I came here. These generally have a SiO 2 +MnO component of 70~
It was 90%. Furthermore, in fillet welding, if the MnO content was less than 38%, deoxidation was likely to be insufficient, and pits and blowholes were likely to occur. On the other hand, MnO/
The SiO2 ratio is related to the melting point and peelability of the slag.
When the amount of SiO 2 is less than 0.8, the melting point of the slag becomes too high and undercuts are likely to occur, and when the amount exceeds 1.3 and the amount of MnO is high or the amount of SiO 2 is low, the slag removability deteriorated. MgO: 3 to 7%; By containing the MgO component at 3% or more,
Slag removability improved. However, when the content exceeds 7%, the viscosity of the molten slag becomes too high, making the arc unstable, undercuts likely to occur, and the bead shape becoming convex, resulting in poor bead appearance. CaF 2 : 1.5 to 4.5%; CaF 2 is a necessary component that decomposes during welding, generates fluorine gas, and serves as a shielding gas generating component that prevents the occurrence of pits, blowholes, etc. If it is less than 1.5%, shielding gas will not be generated enough,
When the content exceeds 4.5%, the slag tends to stick to the bead surface and the slag removability deteriorates. At least one of PbO or Bi2O3 from 0.005 to 0.5
%; Low melting point metal oxides such as PbO and Bi 2 O 3 had the effect of assisting the effect of the MgO component, which improves slag removability. Slag removability tended to improve as the MgO content increased, but slag viscosity also tended to increase as the MgO content increased. However, if at least one of PbO or Bi 2 O 3
Adding 0.005% or more lowers the viscosity of slag and increases the vitality of the slag-metal interface.
The MgO component helped improve the peelability. This effect was the same whether PbO or Bi 2 O 3 was added alone, or both were added in an amount of 0.005% or more. However, when the content is less than 0.005%, the effect is small, and when the content exceeds 0.5%, the viscosity of the slag decreases too much, the flow resistance deteriorates, the bead waveform becomes disordered, and the appearance deteriorates. This deterioration in appearance is due to PbO or Bi 2 O 3
Even if an ingredient is added alone in excess of 0.5%,
The results were the same even when both were added in excess of 0.5%. CaO: 5.0% or less; If CaO content exceeds 5.0% in the flux, slag will easily seize on the bead surface.
Peelability deteriorated. Na 2 O + K 2 O: 0.75% or less; Na 2 O and K 2 O components are contained as impurities in SiO 2 and MnO raw material ores, and as they increase in flux, they affect slag removal performance, bead appearance, Both tended to worsen. Na 2 O + K 2 O exceeds 0.75%,
If it is included in the flux, the arc strength will be weakened and the arc will become unstable, which will disrupt the bead waves and cause slag to become trapped.
It was found that as the bead appearance deteriorated, the slag removability also deteriorated. As mentioned above, the lower the Na 2 O + K 2 O content, the better the bead appearance and slag removability. Even with high MnO- SiO2 fluxes within the above composition range, the flux particles may foam and become porous, resulting in overlay welding in which the upper layer is continuously welded, or when the flux is heated to temperatures above about 150°C. When fillet welding preheated steel plates, the slag removal performance was poor. The flux particle size structure contains 90% by weight or more of flux particles that pass through a sieve with an opening of 1410 μm and do not pass through a sieve with an opening of 149 μm, among which flux particles with an opening of 850 μm,
Weight percentage of flux grains that do not pass through the sieve
The relationship between A and bulk density B of flux is 1.40≦
B≦1.70-1/A-20 (however, A>20); The flux of the present invention is manufactured by mixing and dissolving raw material ores according to the target composition, and then pouring it into a jet water stream and pulverizing it. do. Therefore, the bulk density of the flux particles obtained by the coarse packing method can be reduced by forming the flux particles into needle-shaped, antler-shaped, spherical, or scale-shaped mixed particles, and the particle surface area can be reduced by the same bulk density. Compared to foamed particles, the moisture content is much smaller than that of foamed particles, thereby reducing the amount of moisture adhering to the particle surface and preventing the occurrence of welding defects.
Therefore, even if the particles have the same particle shape, if a large amount of fine particles are included in the flux, the effective surface area of the flux becomes large, and as a result, welding defects cannot be prevented from occurring. Therefore, it is necessary to use a flux containing a large amount of coarse particles that will not cause welding defects. Containing a large amount of flux that does not pass through a sieve with an opening of 1410 μm reduces the shielding effect of the flux, making welding defects more likely to occur.Furthermore, flux containing a large amount of particles that pass through a sieve with an opening of 149 μm reduces the shielding effect of the flux. Since the permeability of gasified gases such as adhered moisture generated during welding deteriorates and defects such as spot marks occur, it is recommended that the content of particles that are too coarse or too fine be less than 10%, which will affect welding performance. It was good and warm. However, for flux grains that are a mixture of needle-shaped, antler-shaped, spherical, or scaly particles, which differ from the conventional particle shape, we measured the bulk density using the rough packing method and determined whether coarse particles or fine particles were used. We believe that there is a problem in measuring only the grain size excluding coarse grains and fine grains.
The welding performance of the prototype flux was investigated regarding the relationship between the content of particles that do not pass through an 850 μm sieve and the bulk density of the coarse packing. As a result, the bulk density of flux with good welding performance is 1.40 g/cm 3 or more,
Aperture that is less than 1.70g/cm 3 and relatively coarse grain
The particle content that does not pass through an 850 μm sieve is 20
It was necessary to exceed %. However, when the bulk density of the entire flux is small, relatively coarse particles
Good welding performance was obtained even with a relatively small amount, but when the bulk density is relatively large, in order to obtain good welding performance, it is necessary not to pass through a sieve with an opening of 850 μm.
Relatively large amounts of relatively coarse flux particles were required. (Example) The effects of the present invention will be described below with reference to Examples.
A prototype flux with the composition and grain size shown in Table 3 was manufactured, and the steel plates shown in Table 1 were assembled as shown in Figure 2. The wire shown in Table 1 was used as a fillet weld test piece, and the wire shown in Table 2 was assembled. Under welding conditions, after preheating the test pieces to 150°C, downward fillet welding was performed, and the slag removal performance and bead appearance of each flux were investigated.

【表】【table】

【表】【table】

【表】 その結果は第4表に示すとおりで、比較フラツ
クスIは、かさ密度と粒度構成が範囲外であり、
スラグ剥離性とビードの波目が粗く、溶接性能が
悪かつた。比較フラツクスJは、かさ密度、粒度
構成が範囲外のため、スラグ剥離性が悪かつた。
比較フラツクスKは、かさ密度、粒度構成が範囲
外のため、ビード外観が悪かつた。比較フラツク
スLも、比較フラツクスKと同様であり、比較フ
ラツクスMも、かさ密度、粒度構成が範囲外で、
スラグ剥離性能、ビード止端部のなじみ性が悪か
つた。比較フラツクスNは、かさ密度が過少であ
ると共に、成分もMgO過多、Bi2O3またはPbO過
少であり、スラグ剥離性、ビード外観の内、波目
が悪かつた。また、比較フラツクス0は、かさ密
度、粒度構成は範囲内であつたが、フラツクス成
分のCaF2、MgOが過少、PbO過多のため、スラ
グ剥離性、ビード外観共悪かつた。比較フラツク
スPは、かさ密度、粒度構成は範囲内であつた
が、成分のCaF2、CaOが過多であり、Na2O+
K2O成分も過多のため、スラグ剥離性、ビード外
観共悪かつた。この様に、比較フラツクスでは、
スラグ剥離性、ビード外観が、いづれも良好なフ
ラツクスはなかつたが、本発明フラツクスでは、
いづれのフラツクスにおいてもスラグ剥離性、ビ
ード外観共良好な性能を示した。
[Table] The results are shown in Table 4. Comparative flux I had bulk density and particle size structure outside the range.
Slag removability and bead waves were rough, and welding performance was poor. Comparative flux J had poor slag removability because the bulk density and particle size structure were outside the range.
Comparative flux K had a poor bead appearance because the bulk density and particle size structure were out of range. Comparative flux L is also similar to comparative flux K, and comparative flux M also has bulk density and particle size structure outside the range,
Slag removal performance and bead toe conformability were poor. Comparative flux N had too little bulk density, too much MgO and too little Bi 2 O 3 or PbO, and had bad slag removability and bad bead appearance. Comparative flux 0 had bulk density and particle size structure within the range, but the flux components CaF 2 and MgO were too low and PbO was too high, resulting in poor slag removability and poor bead appearance. Comparative flux P had bulk density and particle size composition within the range, but the components CaF 2 and CaO were excessive, and Na 2 O +
Since the K 2 O component was also excessive, the slag removability and bead appearance were both poor. In this way, in the comparative flux,
There was no flux that had good slag removability and bead appearance, but the flux of the present invention had
All fluxes showed good performance in terms of slag removability and bead appearance.

【表】【table】

【表】 第4表中の評価基準 (1) スラグ剥離性について、〇印は、スラグが自
然剥離するもの、あるいは、軽打により、スラ
グが除去できるものとし、×印は、スラグが焼
付くものとした。 (2) ビード止端のなじみ性について、〇印は、ビ
ード止端が揃つており、アンダーカツトの発
生、スラグかみ込み等のないもの、×印は、ビ
ード止端部の揃わないもの、または、アンダー
カツト、スラグかみ込みにより、スラグがビー
ド止端部に付着したもの、とした。 (3) ビードの波目については、ビードの波目が細
かく、滑らかで、光沢のあるものを〇印とし、
ビードの波目が粗いもの、あるいは、凸形ビー
ドとなるものを×印とした。 (発明の効果) 以上、詳細に説明したように、本発明フラツク
スは、従来のフラツクスに比べ、フラツクス組成
を限定するとともに、発泡粒子を含まず、比較的
粗粒粒子を多く含有し、しかもかさ密度の小さい
フラツクスとすることにより、従来のフラツクス
より、ビード外観が良好で、スラグ剥離性がさら
に良好であることによつて、溶接能率がさらに向
上する結果、その工業的価値は極めて大きい。
[Table] Evaluation criteria in Table 4 (1) Regarding slag removability, ○ indicates that the slag will peel off naturally or that the slag can be removed by light tapping, and × indicates that the slag will be burned. I took it as a thing. (2) Concerning the conformability of the bead toes, ○ indicates that the bead toes are aligned and there is no undercutting, slag entrapment, etc., and × indicates that the bead toes are not aligned, or The slag adhered to the bead toe due to , undercut, and slag entrainment. (3) Regarding the wavy pattern of the bead, if the wavy pattern of the bead is fine, smooth, and shiny, mark it as ○.
Beads with coarse wavy lines or convex beads were marked with an x. (Effects of the Invention) As described above in detail, the flux of the present invention has a limited flux composition compared to conventional fluxes, does not contain expanded particles, contains relatively large amounts of coarse particles, and is bulky. By using a flux with a low density, the bead appearance is better than that of conventional fluxes, and the slag removability is even better, so welding efficiency is further improved, and as a result, its industrial value is extremely large.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、フラツクスのかさ密度と、フラツク
スの粒度構成、つまりフラツクス中の目開き
850μmのふるいを通過しない、比較的粗粒粒子
含有量が、溶接作業性能に及ぼす影響を示す図、
第2図は、スラグ剥離性能、ビード外観調査のた
めの試験片組立図である。 1:研磨面。
Figure 1 shows the bulk density of the flux and the particle size structure of the flux, that is, the opening in the flux.
A diagram showing the effect of relatively coarse particle content that does not pass through an 850 μm sieve on welding performance,
FIG. 2 is an assembly drawing of a test piece for investigating slag peeling performance and bead appearance. 1: Polished surface.

Claims (1)

【特許請求の範囲】 1 成分が重量パーセントで、SiO2+MnO:70
〜90%、MnO:38%以上、MnO/SiO2:0.8〜
1.3、MgO:3〜7%、CaF2:1.5〜4.5%、PbO
またはBi2O3の少なくとも一方を0.005〜0.5%、
CaO:5.0%以下、Na2O+K2O:0.75%以下、を
含有した高MnO−SiO2系溶融型フラツクスにお
いて、その粒度構成が、目開き1410μmのふるい
を通過し、149μmを通過しないフラツクス粒を
90重量%以上含有し、その内、目開き850μmの
ふるいを通過しないフラツクス粒の含有重量%A
とフラツクスのかさ密度Bとの関係が 1.40≦B≦1.70−1/A−20、(ただし、A>20と する)で表わされる潜弧溶接用溶融型フラツク
ス。
[Claims] 1 Components are weight percent, SiO 2 +MnO: 70
~90%, MnO: 38% or more, MnO/ SiO2 : 0.8~
1.3, MgO: 3-7%, CaF2 : 1.5-4.5%, PbO
or at least one of Bi 2 O 3 at 0.005-0.5%,
In the high MnO-SiO 2 type fused flux containing CaO: 5.0% or less, Na 2 O + K 2 O: 0.75% or less, the particle size structure is such that the flux particles pass through a sieve with an opening of 1410 μm but do not pass through a sieve with an opening of 149 μm. of
Contains 90% by weight or more of flux grains that do not pass through a sieve with an opening of 850 μm (%A)
A melting type flux for submerged arc welding in which the relationship between B and the bulk density of the flux is 1.40≦B≦1.70-1/A-20 (provided that A>20).
JP4843784A 1984-03-14 1984-03-14 Fused flux for submerged arc welding Granted JPS60191692A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4843784A JPS60191692A (en) 1984-03-14 1984-03-14 Fused flux for submerged arc welding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4843784A JPS60191692A (en) 1984-03-14 1984-03-14 Fused flux for submerged arc welding

Publications (2)

Publication Number Publication Date
JPS60191692A JPS60191692A (en) 1985-09-30
JPH0239357B2 true JPH0239357B2 (en) 1990-09-05

Family

ID=12803326

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4843784A Granted JPS60191692A (en) 1984-03-14 1984-03-14 Fused flux for submerged arc welding

Country Status (1)

Country Link
JP (1) JPS60191692A (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5146653A (en) * 1974-10-18 1976-04-21 Tokico Ltd KAMU
JPS56141992A (en) * 1980-04-05 1981-11-05 Kobe Steel Ltd Fused flux for submerged arc welding

Also Published As

Publication number Publication date
JPS60191692A (en) 1985-09-30

Similar Documents

Publication Publication Date Title
US5300754A (en) Submerged arc flux and method of making same
US3177340A (en) Flux-cored electrode and process of welding
US4764224A (en) Baked flux for submerged arc welding
JP3392347B2 (en) Sintered flux for submerged arc welding and method for producing the same
JPH0130597B2 (en)
JPH0468079B2 (en)
JP3433681B2 (en) Sintered flux for submerged arc welding and method for producing the same
CN112222682B (en) High-fluorine-alkali type powder, preparation method and self-shielded flux-cored wire
JP2003245794A (en) Manufacturing method of fired flux for submerged arc welding
JPH0239357B2 (en)
US2785094A (en) Coated copper alloy arc welding electrode
US4340805A (en) Welding electrode with a fluoride based slag system
JP3577995B2 (en) Manufacturing method of fired flux for submerged arc welding
CN104339101B (en) One side solder flux used for submerged arc welding
JPS5937719B2 (en) Sintered flux for submerged arc welding
JPS5841694A (en) Calcined flux for submerged arc welding
JP3551082B2 (en) Fired flux for submerged arc welding
JPS6352794A (en) Baked flux for submerged arc welding
JP6837420B2 (en) Flux for submerged arc welding
JPH0284295A (en) Flux cored wire for self-shielded arc welding
JPH0455790B2 (en)
JPH05237691A (en) Arc welding electrode for coating cast iron
JPH06269989A (en) Low-hydrogen coated arc welding rod
JPH059197B2 (en)
JPS63264297A (en) Flux for non-fused submerged arc welding