JP2000334596A - Manufacturing method of fired flux for submerged arc welding - Google Patents
Manufacturing method of fired flux for submerged arc weldingInfo
- Publication number
- JP2000334596A JP2000334596A JP11144686A JP14468699A JP2000334596A JP 2000334596 A JP2000334596 A JP 2000334596A JP 11144686 A JP11144686 A JP 11144686A JP 14468699 A JP14468699 A JP 14468699A JP 2000334596 A JP2000334596 A JP 2000334596A
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- flux
- temperature
- submerged arc
- arc welding
- firing
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Abstract
(57)【要約】
【課題】 高速溶接時においても、ガスの発生を効果的
に抑制して、耐ポックマーク性に優れるだけでなく、良
好な溶接作業性を有するサブマージアーク溶接用の高温
焼成型フラックスを提供する。
【解決手段】 焼成型フラックス原料粉末を、造粒後、
750℃を超える温度で焼成してサブマージアーク溶接用
フラックスを製造するに際し、 700℃以上、(最高温度
−50℃)以下の温度域を5℃/min以上の昇温速度で昇温
する。(57) [Summary] [Problem] High-temperature sintering for submerged arc welding not only having excellent pock mark resistance but also having good welding workability by effectively suppressing gas generation even during high-speed welding. Provide mold flux. SOLUTION: After sintering type flux raw material powder is granulated,
When producing a flux for submerged arc welding by firing at a temperature exceeding 750 ° C., the temperature is raised from 700 ° C. to (maximum temperature −50 ° C.) at a rate of 5 ° C./min or more.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、船舶、海洋構造
物、貯槽、鉄骨および橋梁等の鋼構造物の溶接に用いて
好適なサブマージアーク溶接用焼成型フラックスの製造
方法に関し、とくに建築用鉄骨の梁などに用いられる溶
接組立式H型部材の隅肉継手溶接を高速サブマージアー
ク溶接で行う場合等において、欠陥のない溶接部が安定
して得られる優れた溶接作業性を有するサブマージアー
ク溶接用焼成型フラックスの製造方法に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a fired flux for submerged arc welding suitable for welding steel structures such as ships, marine structures, storage tanks, steel frames, bridges, etc. For high-speed submerged arc welding of fillet joints of weldable H-type members used for beams, etc., for submerged arc welding with excellent welding workability that can stably obtain defect-free welds The present invention relates to a method for producing a fired flux.
【0002】[0002]
【従来の技術】サブマージアーク溶接(潜弧溶接)用フ
ラックスは、通常、2酸化ケイ素(SiO 2)を主体とし、そ
れに酸化マグネシウム (MgO) 、マンガン酸化物 (Mn
O、Mn30 4 等) 、酸化カルシウム (CaO) 、アルミナ(A
l203) およびその他の酸化物、ふっ化物等を添加配合し
て製造されている。そして、このサブマージアーク溶接
用フラックスは、その製造方法の違いにより、溶融型フ
ラックス、焼成型フラックス(焼結型フラックスも含
む、以下同じ)および混合型フラックスに分類される。2. Description of the Related Art Submerged arc welding (submerged arc welding)
Lux is usually silicon dioxide (SiO Two).
Magnesium oxide (MgO), manganese oxide (Mn
O, MnThree0 Four Etc.), calcium oxide (CaO), alumina (A
lTwo0Three) And other oxides, fluorides, etc.
Manufactured. And this submerged arc welding
Flux can be produced by melting mold flux depending on the manufacturing method.
Flux, fired flux (including sintered flux)
And the same shall apply hereinafter) and mixed fluxes.
【0003】このうち焼成型フラックスは、一般に、酸
化物やふっ化物等のフラックス原料粉に結合剤(バイン
ダ)として水ガラス(珪酸ソーダ)などを添加し、混
練、造粒、乾燥、焼成という工程を経て製造されてい
る。まれに、結合剤が省略される場合もある。このよう
な焼成型フラックスは、比較的簡単な設備で製造可能な
ために安価なだけでなく、脱酸剤や合金元素の添加が可
能なために溶接金属成分を調整できるという利点があ
る。[0003] Among them, the calcination type flux generally includes a process of adding water glass (sodium silicate) or the like as a binder (binder) to a flux raw material powder such as an oxide or a fluoride, and kneading, granulating, drying and firing. It has been manufactured through. In rare cases, the binder may be omitted. Such a sintering type flux has an advantage that it can be manufactured with relatively simple equipment and thus is inexpensive, and that a welding metal component can be adjusted because a deoxidizing agent and an alloy element can be added.
【0004】しかしながら、この焼成型フラックスは、
原料によってフラックスの品質ひいては溶接部の特性が
大きく変化する。例えば、ピットやポックマーク等の溶
接欠陥が溶接部に発生する。これらの溶接欠陥は、原料
中の結晶水等の水分または原料酸化物が酸素源となり、
溶接時に生じるCO,CO2 ガスに起因して発生するもので
ある。[0004] However, this calcined flux is
The quality of the flux, and thus the properties of the weld, vary greatly depending on the raw material. For example, welding defects such as pits and pock marks occur at the welded portions. These welding defects are caused by moisture such as water of crystallization in the raw material or raw material oxides,
It is generated due to CO and CO 2 gas generated during welding.
【0005】上記の問題に対して、低温(700℃以下) で
焼成する低温焼成型フラックスでは、フラックス中に炭
酸塩や脱酸剤を添加することによって耐溶接欠陥性の改
善を図ってきた。これに対し、高温(700〜1200℃) で焼
成する高温焼成型フラックスは、炭酸塩を用いずに溶着
金属の低水素化が図れるため、高速溶接性には優れるも
のの、使用可能な脱酸剤の種類が非常に限られているこ
ともあって、耐ポックマーク性は劣っていた。しかも、
その検討はほとんど行われていないのが現状である。[0005] In order to solve the above problem, in a low-temperature firing type flux which is fired at a low temperature (700 ° C. or lower), improvement in welding defect resistance has been attempted by adding a carbonate or a deoxidizing agent to the flux. On the other hand, a high-temperature firing flux that fires at a high temperature (700 to 1200 ° C) can reduce the hydrogen content of the deposited metal without using a carbonate, and although it has excellent high-speed weldability, it can be used as a deoxidizing agent. Was very poor, and the pock mark resistance was poor. Moreover,
At present, little has been considered.
【0006】脱酸を目的として金属粉を添加する例とし
ては、例えば特公昭32−409 号公報や特公昭44−13249
号公報に、Fe−SiおよびSi−Mnの例が記載されている。
高温焼成型フラックスでは、高温焼成時に脱酸剤が変質
(酸化や窒化)して脱酸剤としての作用効果が減退する
場合が多いことから、脱酸剤として使用されているのは
この2種類が主である。しかしながら、このFe−Siおよ
びSi−Mnを脱酸剤として用いた場合でも、高温焼成条件
等により脱酸剤が変質したり、フラックスを繰り返し使
用した場合に安定して良好な耐ポックマーク性や優れた
溶接作業性が得られないなどの問題を残していた。Examples of adding metal powder for the purpose of deoxidation include, for example, Japanese Patent Publication No. 32-409 and Japanese Patent Publication No. 44-13249.
In the publication, examples of Fe-Si and Si-Mn are described.
In high-temperature sintering fluxes, the deoxidizing agent is often degraded (oxidized or nitrided) during high-temperature sintering and the effect of the deoxidizing agent is reduced, so these two types of deoxidizing agents are used. Is the main. However, even when Fe-Si and Si-Mn are used as the deoxidizing agent, the deoxidizing agent is deteriorated due to high-temperature sintering conditions or the like. Problems such as not being able to obtain excellent welding workability remain.
【0007】その他、特開昭62−68695 号公報には、フ
ラックス中のSiが 0.5wt%以下の高温焼成型フラックス
が開示されている。しかしながら、この技術は、フラッ
クス中のSi量を 0.5wt%以下に抑制することによって、
高温焼成時における脱酸剤の変質による溶接作業性への
影響を少なくしたもので、脱酸剤およびフラックスの焼
成方法等は検討されていない。In addition, Japanese Patent Application Laid-Open No. 62-68695 discloses a high-temperature sintering type flux containing 0.5 wt% or less of Si in the flux. However, this technology reduces the amount of Si in the flux to 0.5 wt% or less,
The effect of deterioration of the deoxidizer during high-temperature firing on welding workability is reduced, and a method of firing the deoxidizer and flux has not been studied.
【0008】[0008]
【発明が解決しようとする課題】本発明は、上述した現
状に鑑み開発されたもので、脱酸剤としてFe−Siを使用
し、造粒後の焼成処理の際、 700℃以上の温度域におけ
る昇温速度を制御することによって、欠陥のない溶接部
が安定して得られ、優れた溶接作業性を有するサブマー
ジアーク溶接用焼成型フラックスの有利な製造方法を提
案することを目的とする。SUMMARY OF THE INVENTION The present invention has been developed in view of the above-mentioned situation, and uses Fe-Si as a deoxidizing agent. It is an object of the present invention to propose an advantageous method for producing a fired flux for submerged arc welding having a stable welded portion free from defects by controlling the rate of temperature rise in the above-mentioned method and having excellent welding workability.
【0009】[0009]
【課題を解決するための手段】さて、発明者らは、750
℃以上の温度で焼成するサブマージアーク溶接用焼成型
フラックスの製造に際し、欠陥のない溶接部を安定して
得る方法について鋭意検討した結果、脱酸を目的として
Fe−Siを添加するフラックスでは、製造時の焼成条件の
最適化が溶接時における作業性の改善および欠陥発生の
抑制に有効であることを見出した。本発明は、上記知見
に立脚するものである。Means for Solving the Problems Now, the inventors have studied 750
In the production of firing flux for submerged arc welding, which is fired at a temperature of ℃ or more, as a result of earnestly examining a method for stably obtaining defect-free welds,
With the flux to which Fe-Si is added, it has been found that optimizing the firing conditions during production is effective for improving workability during welding and suppressing the occurrence of defects. The present invention is based on the above findings.
【0010】すなわち、本発明の要旨構成は次のとおり
である。 1.焼成型フラックス原料粉末を、造粒後、 750℃を超
える温度で焼成してサブマージアーク溶接用フラックス
を製造するに際し、 700℃以上、(最高温度−50℃)以
下の温度域を5℃/min以上の昇温速度で昇温し、焼成す
ることを特徴とするサブマージアーク溶接用焼成型フラ
ックスの製造方法。That is, the gist of the present invention is as follows. 1. After granulating the sintering type flux raw material powder and firing at a temperature exceeding 750 ° C to produce a flux for submerged arc welding, the temperature range of 700 ° C or more and (maximum temperature -50 ° C) or less is 5 ° C / min. A method for producing a fired flux for submerged arc welding, characterized in that the temperature is raised at the above-mentioned heating rate and then fired.
【0011】2.上記1において、フラックス成分が、
total SiO2:30〜70wt%、マンガン酸化物(MnO量換算
で) :5〜40wt%、MgO:3〜30wt%、A1203 :2〜20
wt%を含む組成になるサブマージアーク溶接用焼成型フ
ラックスの製造方法。2. In the above item 1, the flux component is
total SiO 2: 30~70wt%, manganese oxide (in amount of MnO terms): 5~40wt%, MgO: 3~30wt %, A1 2 0 3: 2~20
A method for producing a firing flux for submerged arc welding having a composition containing wt%.
【0012】3.脱酸剤として、Si含有量が30〜80wt%
であって、かつ粒径:106 μm 超が重量比率で10%以
下、粒径:45μm 未満が重量比率で50%以下の粒度分布
を有するFe−Si粒子を、1〜10wt%の割合で配合した焼
成型フラックス原料を、造粒後、750 ℃以上の温度で焼
成を施して成るサブマージアーク溶接用フラックスの製
造方法において、焼成に際し、 700℃以上、(最高温度
−50℃)以下の温度域を5℃/min以上の昇温速度で昇温
することを特徴とするサブマージアーク溶接用焼成型フ
ラックスの製造方法。3. As deoxidizer, Si content is 30 ~ 80wt%
And Fe-Si particles having a particle size distribution of 10% or less by weight when the particle size is more than 106 μm and 50% or less by weight when the particle size is less than 45 μm are blended in a ratio of 1 to 10% by weight. In the method for manufacturing a flux for submerged arc welding, which is performed by granulating the fired type flux raw material and firing at a temperature of 750 ° C or higher, the temperature range of 700 ° C or higher and (maximum temperature -50 ° C) At a heating rate of 5 ° C./min or more.
【0013】[0013]
【発明の実施の形態】以下、本発明を具体的に説明す
る。まず、本発明を由来するに至った経緯を実験結果に
基づいて説明する。表1に示すような配合比率になるよ
うに調整した原料を、水ガラスを結合剤として12〜200
メッシュに造粒し、1100℃, 5分の条件で焼成した。こ
の際、フラックスの焼成は定置式バッチ炉を用いて行
い、フラックス焼成時の昇温速度の影響について調査し
た。なお、昇温速度は、フラックス充填層内で平均的昇
温速度位置と考えられる、フラックス充填容器の中央部
の表面より充填高さの1/4の箇所の温度を熱電対を用
いて測定し、 700〜1050℃の温度域での平均昇温速度を
求めた。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be specifically described below. First, the circumstances that led to the invention will be described based on experimental results. Raw materials adjusted to have the compounding ratios as shown in Table 1 were mixed with water glass as a binder in an amount of 12-200.
The mixture was granulated into a mesh and fired at 1100 ° C. for 5 minutes. At this time, the flux was fired using a stationary batch furnace, and the effect of the temperature rising rate during the flux firing was investigated. The heating rate was measured using a thermocouple at a temperature that was considered to be the average heating rate position in the flux-packed layer and that was 1/4 of the filling height from the surface of the central part of the flux-filled container. The average rate of temperature rise in the temperature range of 700 to 500 ° C. was determined.
【0014】これらのフラックスと、2wt%Mn系ワイヤ
(4.8mmφ)を用い、溶接電流:750A,溶接電圧:35
V,溶接速度:40cm/minの溶接条件で、SS400 相当の鋼
板を下向き隅肉シングル溶接し、ビード外観を調査し
た。得られた結果を表2に示すが、同表から明らかなよ
うに、フラックス焼成時の昇温速度が溶接ビード外観に
及ぼす影響は極めて大きいことが分かる。These fluxes and 2 wt% Mn-based wire
(4.8mmφ), welding current: 750A, welding voltage: 35
V, welding speed: 40cm / min, under welding conditions, SS400 equivalent steel plate was subjected to single downward fillet welding and the bead appearance was investigated. The obtained results are shown in Table 2. As is clear from the table, it can be seen that the effect of the rate of temperature rise during flux firing on the appearance of the weld bead is extremely large.
【0015】[0015]
【表1】 [Table 1]
【0016】[0016]
【表2】 [Table 2]
【0017】フラックス焼成時の昇温速度が溶接ビード
外観と密接な関係がある理由としては、次のようなこと
が考えられる。通常、脱酸を目的として高温焼成型フラ
ックスに添加される金属粉としては、Fe−SiおよびSi−
Mnが一般に知られているが、これらも 700℃以上の温度
域では、反応速度は遅いものの、徐々に変質(酸化)し
て脱酸剤としての作用効果が減退する。この点、 700℃
以上の温度域における昇温速度を5℃/min以上にする
と、最高温度付近での脱酸剤の酸化速度に影響を及ぼす
ような脱酸剤酸化挙動に変化(昇温時の酸化量が少な
く、またその酸化進行を遅らせる)が生じ、その結果、
脱酸剤の酸化ロスが格段に低減するものと考えられる。The reason why the rate of temperature rise during flux firing is closely related to the appearance of the weld bead may be as follows. Usually, as the metal powder added to the high-temperature firing type flux for the purpose of deoxidation, Fe-Si and Si-
Mn is generally known, but also in the temperature range of 700 ° C. or higher, although the reaction rate is slow, the quality gradually changes (oxidizes) and the effect as a deoxidizing agent decreases. 700 ° C
When the temperature rise rate in the above temperature range is 5 ° C / min or more, the deoxidizer oxidation behavior changes which affects the oxidation rate of the deoxidizer near the maximum temperature. , And also slows down its oxidation),
It is considered that the oxidation loss of the deoxidizing agent is significantly reduced.
【0018】以下、本発明における構成要件を、前記の
範囲に限定した理由について説明する。本発明では、焼
成工程の昇温過程において、 700℃以上、(最高温度−
50℃)以下の温度域を5℃/min以上の昇温速度で昇温す
る必要がある。まず、昇温速度を制御すべき温度範囲の
下限を 700℃としたのは、温度が 700℃以上になると、
上述したとおり、Fe−Si粒子の変質(酸化)が懸念され
るからである。一方、フラックス粉体は熱伝達性があま
り良くないので、均熱により均一材質とするには均熱温
度域(最高温度〜最高温度−50℃の温度域)において少
なくとも5分程度の均熱処理が必要である。従って、か
かる均熱温度域に至るまでの昇温過程における温度範囲
の上限として(最高温度−50℃)を定めた。また、かか
る温度域における昇温速度を5℃/min以上に限定したの
は、昇温速度が5℃/min未満ではFe−Si粒子が変質(酸
化)して、溶接時における脱酸効果が小さくなるからで
ある。Hereinafter, the reason why the constituent elements in the present invention are limited to the above range will be described. In the present invention, in the heating process of the firing step, the temperature is 700 ° C. or more (the maximum temperature −
It is necessary to raise the temperature in the temperature range below 50 ° C) at a rate of 5 ° C / min or more. First, the lower limit of the temperature range in which the heating rate should be controlled was set at 700 ° C.
As described above, the alteration (oxidation) of the Fe-Si particles is concerned. On the other hand, since the heat transfer property of the flux powder is not so good, it is necessary to perform a soaking treatment for at least about 5 minutes in a soaking temperature range (a temperature range from a maximum temperature to a maximum temperature of −50 ° C.) in order to obtain a uniform material by the soaking. is necessary. Therefore, (maximum temperature −50 ° C.) was determined as the upper limit of the temperature range in the heating process up to the soaking temperature range. In addition, the reason why the heating rate in this temperature range is limited to 5 ° C./min or more is that when the heating rate is less than 5 ° C./min, the Fe—Si particles are altered (oxidized), and the deoxidizing effect during welding is reduced. This is because it becomes smaller.
【0019】次に、原料配合時に、脱酸剤として用いる
Fe−Siが備えるべき条件について説明する。 Fe−SiのSi含有量:30〜80wt% Si含有量が80wt%を超えると、添加するFe−Siの絶対量
が少量となりフラックス全体に均一に分布させるのが困
難となるため、80wt%以下とした。また、Si含有量が30
wt%未満では、Fe−Siを多量に添加する必要が生じ、そ
の多量添加によりフラックス中の鉄分が増大し、これが
原因となって溶接ビード表面性状が劣化するので、30wt
%以上にした。Next, it is used as a deoxidizing agent when compounding the raw materials.
The conditions that Fe-Si should have will be described. Si content of Fe-Si: 30 to 80 wt% If the Si content exceeds 80 wt%, the absolute amount of Fe-Si to be added becomes small, making it difficult to distribute uniformly throughout the flux. And In addition, the Si content is 30
If it is less than wt%, it is necessary to add a large amount of Fe-Si, and the addition of a large amount increases the iron content in the flux, which deteriorates the surface properties of the weld bead.
% Or more.
【0020】Fe−Siの粒度構成:106 μm を超える粒子
の割合が10wt%以下で、かつ45μm 未満の粒子の割合が
50wt%以下 Fe−Si粒子のうち、106 μm を超える粒子の割合が10wt
%を超えると繰り返し利用していくうちに脱酸効果およ
び脱酸効率が低下して、ポックマークが出易くなるた
め、10wt%以下に限定した。一方45μm 未満の粒子の割
合が50wt%以上になると高温焼成時に細かいFe−Siの粒
子が酸化消失するため、50wt%以下に限定した。Particle size composition of Fe—Si: The proportion of particles exceeding 106 μm is 10 wt% or less and the proportion of particles less than 45 μm is
50 wt% or less Of the Fe-Si particles, the ratio of particles exceeding 106 μm is 10 wt%
%, The deoxidizing effect and the deoxidizing efficiency decrease during repeated use, and a pock mark is likely to appear. Therefore, the content is limited to 10 wt% or less. On the other hand, when the proportion of particles having a particle size of less than 45 μm is 50 wt% or more, fine Fe—Si particles are oxidized and disappeared during high-temperature sintering.
【0021】フラックス中におけるFe−Siの含有量:1
〜10wt% フラックス全体に対してFe−Siの含有量が1wt%に満た
ないと所望の脱酸効果が得られず、一方10wt%を超えて
添加しても脱酸効果は飽和に達するので、Fe−Si含有量
は1〜10%の範囲に限定した。Content of Fe—Si in flux: 1
If the Fe-Si content is less than 1 wt% with respect to the entire flux, the desired deoxidizing effect cannot be obtained. On the other hand, even if it exceeds 10 wt%, the deoxidizing effect reaches saturation. The Fe-Si content was limited to the range of 1 to 10%.
【0022】本発明では、サブマージアーク溶接用フラ
ックスの製造に当たり、基本的に、700℃以上、(最高
温度−50℃)以下の温度域における昇温速度を5℃/min
以上に規制することにより、また好ましくはさらに、フ
ラックス中に脱酸剤として添加するFe−Si粒子につい
て、その成分、粒度構成および添加量を上記の範囲に制
限することによって、所望の効果を得ることができる
が、焼成型フラックスのその他の代表組成については、
次のとおりである。In the present invention, when producing the flux for submerged arc welding, basically, the heating rate in the temperature range of 700 ° C. or more and (maximum temperature −50 ° C.) or less is 5 ° C./min.
By restricting as described above, and preferably, further, for Fe-Si particles added as a deoxidizing agent in the flux, the desired effects are obtained by restricting the components, the particle size composition and the amount of addition to the above ranges. However, for other typical compositions of calcined flux,
It is as follows.
【0023】total SiO2:30〜70wt% SiO2は、ビード外観を良好に保つための造滓剤として添
加する。しかしながら、total SiO2が30wt%未満ではそ
の添加効果に乏しく、特に高速隅肉溶接のようにビード
端部のなじみが重要な場合には、30wt%未満では良好な
ビード形状を保持できない。一方、70wt%を超えて多量
に含まれると粘性が高くなりすぎてかえってビード外観
が乱れ易くなり、またスラグの剥離性が劣化するなどの
不具合が生じる。従って、total SiO2量は30〜70wt%程
度とするのが好ましい。Total SiO 2 : 30 to 70 wt% SiO 2 is added as a slag-making agent to keep the bead appearance good. However, if the total SiO 2 content is less than 30 wt%, the effect of the addition is poor. In particular, in the case where penetration of the bead end is important such as high-speed fillet welding, a good bead shape cannot be maintained at less than 30 wt%. On the other hand, if it is contained in a large amount exceeding 70% by weight, the viscosity becomes too high, and the bead appearance tends to be disturbed, and the slag peeling property is deteriorated. Therefore, it is preferable that the total SiO 2 amount be about 30 to 70 wt%.
【0024】マンガン酸化物:5〜40wt%(MnO量換算
で) 隅肉溶接用フラックスとしては、溶接速度が速くなって
もビード端部のなじみが良好である必要がある。そのた
めには、マンガン酸化物を含有するスラグとすることが
好適であるが、添加量がMnO量換算で5wt%に満たない
とその効果が認められず、一方40wt%を超えて含有され
ると溶融池でCO反応が激しくなる結果、ビード外観が劣
化するので、マンガン酸化物量は5〜40wt%程度とする
ことが好ましい。Manganese oxide: 5 to 40% by weight (in terms of MnO content) As a fillet welding flux, it is necessary that the bead ends conform well even if the welding speed is increased. For that purpose, it is preferable to use a slag containing manganese oxide. However, if the added amount is less than 5 wt% in terms of the amount of MnO, the effect is not recognized, and if the added amount exceeds 40 wt%. As the CO reaction intensifies in the molten pool, the bead appearance deteriorates. Therefore, the amount of manganese oxide is preferably about 5 to 40 wt%.
【0025】MgO:3〜30wt% MgOは、スラグの融点および粘性を調整し、スラグ剥離
性を確保するのに有用な成分である。しかしながら、含
有量が3wt%未満では十分な効果が得られず、一方30wt
%を超えると粘性が低下しすぎたり、融点が上昇しすぎ
てビード外観が劣化する傾向が現れる。それ故、MgOは
3〜30wt%程度とするのが望ましい。MgO: 3 to 30 wt% MgO is a component useful for adjusting the melting point and viscosity of the slag and ensuring the slag removability. However, if the content is less than 3 wt%, a sufficient effect cannot be obtained.
%, The viscosity tends to be too low, and the melting point tends to be too high, and the bead appearance tends to deteriorate. Therefore, MgO is desirably about 3 to 30% by weight.
【0026】Al203 :2〜 20 wt% Al203 は、スラグの粘性および融点を調整する上で重要
な成分であるが、2wt%未満ではその添加効果に乏し
く、一方20wt%を超えると融点が上昇しすぎてビード形
状の劣化を招くので、含有量は2〜20wt%程度とするの
が望ましい。Al 2 O 3 : 2 to 20 wt% Al 2 O 3 is an important component for adjusting the viscosity and melting point of the slag, but if it is less than 2 wt%, the effect of its addition is poor. If it exceeds, the melting point rises too much and the bead shape is deteriorated, so that the content is desirably about 2 to 20% by weight.
【0027】また、その他に、CaOやCaF2を含有させる
ことも好ましい。 CaO:10wt%以下 CaOは、スラグの流動性に影響を及ぼす成分であり、10
wt%を超えて多量に含有されると流動性が阻害されてビ
ード形状の劣化を招くので、CaOは10wt%以下程度とす
るのが好ましい。In addition, it is also preferable to contain CaO or CaF 2 . CaO: 10 wt% or less CaO is a component that affects the fluidity of slag.
If it is contained in a large amount in excess of wt%, the fluidity is impaired and the bead shape is degraded, so CaO is preferably set to about 10 wt% or less.
【0028】CaF2:15wt%以下 CaF2は、スラグの流動性を向上させる成分であるが、15
wt%を超えるとスラグが流動し易くなるので、CaF2は15
wt%以下程度とするのが望ましい。なお、特に好ましい
範囲は5wt%以下である。CaF 2 : 15 wt% or less CaF 2 is a component that improves the fluidity of slag.
If it exceeds wt%, the slag will flow more easily, so CaF 2
It is desirable to set it to about wt% or less. Note that a particularly preferable range is 5% by weight or less.
【0029】以上、代表的なフラックス組成について説
明したが、その他にも必要に応じてTiO2:10wt%以下、
BaO:5wt%以下、ZrO2:5wt%以下、B203:4wt%以
下、CaCO3:5wt%以下から選ばれる1種以上を添加し
ても良い。TiO2は、溶接中に還元され、溶接金属中へTi
が移行して溶接金属の靱性を向上させる作用がある。し
かしながら、10wt%を超えるとかえって靱性を劣化させ
る。BaO,ZrO2は、スラグの塩基度や融点を調整するた
めに添加する。しかしながら、5wt%を超える添加はい
ずれもビード外観やスラグ剥離性を劣化させる。B20
3は、溶接中の還元反応により、溶接金属中にBが移行
して溶接金属の靱性改善に寄与する。しかしながら、4
wt%を超えると溶着金属の凝固割れを助長する。CaCO3
は、溶接中に分解して CO2を発生し、水素分圧を下げる
ため溶接金属中の水素量の低減に有効である。しかしな
がら、5wt%を超えるとビード外観を劣化させる。The typical flux composition has been described above. However, if necessary, TiO 2 : 10 wt% or less,
BaO: 5 wt% or less, ZrO 2: 5wt% or less, B 2 0 3: 4wt% or less, CaCO 3: may be added one or more selected from the following 5 wt%. TiO 2 is reduced during welding and Ti
Has the effect of improving the toughness of the weld metal. However, if it exceeds 10% by weight, the toughness is rather deteriorated. BaO and ZrO 2 are added to adjust the basicity and melting point of the slag. However, any addition exceeding 5 wt% deteriorates bead appearance and slag removability. B 2 0
In No. 3 , B is transferred into the weld metal due to a reduction reaction during welding, thereby contributing to improvement in toughness of the weld metal. However, 4
If it exceeds wt%, solidification cracking of the deposited metal is promoted. CaCO 3
Decomposes during welding to generate CO 2 and reduce the hydrogen partial pressure, which is effective in reducing the amount of hydrogen in the weld metal. However, if it exceeds 5% by weight, the bead appearance deteriorates.
【0030】上述した好適組成となるようにフラックス
原料粉と、前述した成分および粒度構成に調整されたFe
−Siとを適正量添加、配合して、結合剤と共に混練した
後、造粒し、ついで前述した焼成条件で焼成する。造粒
法はとくに限定しないが、転動式造粒機や押し出し式造
粒機を用いるのが好ましい。造粒したのち、ダストの除
去や粗大粒の解砕などの整粒処理を行って、粒子径:0.
075 〜2.5 mmの大きさの粒子にするのが好ましい。整粒
処理は焼成後に行っても良い。なお、結合剤(バイン
ダ)としては、ポリビニルアルコールなどの水溶液や水
ガラスが好適である。中でも、従来から用いられている
SiO2とNa2Oのモル比:1〜5の珪酸ソーダ(水ガラス)
が有利に適合する。また、水ガラス使用量はフラックス
原料1kgあたり80〜150 cc程度でよい。また、焼成温度
については、焼成温度が 750℃を下回ると結合剤(バイ
ンダ)より持ち込まれた水分の乾燥が不十分となり、溶
着金属中拡散性水素の増加を招くので、焼成温度は 750
℃以上とする必要がある。なお、焼成は、ロータリーキ
ルン、定置式バッチ炉およびベルト式焼成炉などを用い
て行う。The flux raw material powder and the Fe and Fe particles adjusted to the above-mentioned components and particle size composition so as to have the above-mentioned preferred composition are provided.
After adding and blending an appropriate amount of Si and kneading with a binder, granulating, and then firing under the firing conditions described above. The granulation method is not particularly limited, but it is preferable to use a rolling granulator or an extrusion granulator. After granulation, sizing processing such as dust removal and crushing of coarse particles is performed to obtain a particle size of 0.
It is preferred that the particles have a size between 075 and 2.5 mm. The sizing process may be performed after firing. In addition, as the binder (binder), an aqueous solution such as polyvinyl alcohol or water glass is preferable. Above all, it has been used
Molar ratio of SiO 2 to Na 2 O: 1 to 5 sodium silicate (water glass)
Is advantageously fitted. The amount of water glass used may be about 80 to 150 cc per 1 kg of the flux material. Regarding the firing temperature, if the firing temperature is lower than 750 ° C, the moisture brought in from the binder (binder) will not be sufficiently dried, causing an increase in the diffusible hydrogen in the deposited metal.
It is necessary to be higher than ° C. The firing is performed using a rotary kiln, a stationary batch furnace, a belt-type firing furnace, or the like.
【0031】[0031]
【実施例】実施例1 表1に示したような比率になるように配合した原料を、
水ガラスを結合剤として12〜200 メッシュに造粒し、10
00℃、5分の条件で焼成した。Fe−Siとしては、106 μ
m 超が10wt%以下、45μm 未満が50wt%以下の粒度分布
を有し、Si含有量が18〜76wt%のものを用いた。なお、
フラックスの焼成はロータリーキルンにより行い、 700
〜950 ℃の温度域における平均昇温速度は12℃/minであ
った。なお、昇温速度は、10mm角の鉄片を付けた熱電対
を用いて測定した。これらのフラックスと2wt%Mn系ワ
イヤ(4.8mmφ)を用いて、溶接電流:850A, 溶接電
圧:40V, 溶接速度:50cm/minの溶接条件で、SM400 相
当の鋼板に対して下向き隅肉溶接を行い、ビード外観に
ついて調査した。得られた結果を表3に示す。EXAMPLES Example 1 Raw materials blended so as to have the ratios shown in Table 1 were prepared.
Granulate to 12-200 mesh using water glass as binder, 10
It baked on conditions of 00 degreeC and 5 minutes. 106 μm for Fe-Si
Those having a particle size distribution of more than 10 wt% or less than m and 50 wt% or less for less than 45 μm and having an Si content of 18 to 76 wt% were used. In addition,
The flux is baked in a rotary kiln, 700
The average heating rate in the temperature range of 950950 ° C. was 12 ° C./min. The heating rate was measured using a thermocouple with a 10 mm square iron piece. Using these fluxes and 2wt% Mn-based wire (4.8mmφ), under the welding conditions of welding current: 850A, welding voltage: 40V, welding speed: 50cm / min, downward fillet welding was performed on a steel plate equivalent to SM400. The bead appearance was examined. Table 3 shows the obtained results.
【0032】[0032]
【表3】 [Table 3]
【0033】同表から明らかなように、焼成時における
昇温速度、さらにはFe−Siの成分および添加量が本発明
の適正範囲を満足するフラックス(No.2, 3)を用いた場
合には良好なビード外観を得ることができた。これに対
し、Fe−Si中のSi含有量が適正範囲に満たないもの(N
o.1)は、ポックマーク発生個数が適合例に比べると非
常に多く、ビード表面性状が格段に劣っていた。As is clear from the table, when the flux (No. 2, 3) in which the rate of temperature rise during firing, and furthermore, the composition and amount of Fe—Si satisfy the appropriate range of the present invention, are used. Obtained a good bead appearance. On the other hand, when the Si content in Fe-Si is less than the appropriate range (N
In o.1), the number of occurrences of pock marks was much larger than that of conforming cases, and the bead surface properties were remarkably inferior.
【0034】実施例2 表4に示す組成のオリビンサンドを用いて、表5に示す
比率になるように配合した原料を、水ガラスを造粒剤と
して混練し、12〜200 メッシュに造粒後、乾燥、焼成し
たのち、粒度調整を行い、フラックスを得た。フラック
スの焼成はベルト式焼成炉により行い、 900℃、5分の
条件で焼成した。炉内におけるフラックス充填層厚は変
化させず、炉内への投入量、ベルト速度および炉内設定
温度を変化させることにより、フラックス焼成時の昇温
速度を変化させた。なお、フエロシリコンとしては、粒
度分布を調整したFe−47wt%Siを用いた。これらのフラ
ックスと2wt%Mn系ワイヤ(4.8mmφ)を用いて、溶接電
流:900A, 溶接電圧:40V, 溶接速度:60cm/minの溶
接条件で、SS400 相当の鋼板に対して下向き隅肉シング
ル溶接を行い、ビード外観について調査した。得られた
結果を表6に示す。Example 2 Raw materials prepared by using olivine sand having the composition shown in Table 4 so as to have the ratio shown in Table 5 were mixed with water glass as a granulating agent, and granulated to 12 to 200 mesh. After drying and firing, the particle size was adjusted to obtain a flux. The flux was fired in a belt-type firing furnace at 900 ° C. for 5 minutes. The rate of temperature rise during flux firing was changed by changing the amount charged into the furnace, the belt speed, and the set temperature in the furnace without changing the thickness of the flux-filled layer in the furnace. In addition, Fe-47wt% Si whose particle size distribution was adjusted was used as the fuero silicon. Using these fluxes and 2wt% Mn-based wire (4.8mmφ), welding current: 900A, welding voltage: 40V, welding speed: 60cm / min. , And the bead appearance was examined. Table 6 shows the obtained results.
【0035】[0035]
【表4】 [Table 4]
【0036】[0036]
【表5】 [Table 5]
【0037】[0037]
【表6】 [Table 6]
【0038】表6から明らかなように、本発明の要件を
満足する条件で製造したフラックスを用いた場合には、
良好なビード外観を得ることができた。As is clear from Table 6, when the flux manufactured under the conditions satisfying the requirements of the present invention is used,
A good bead appearance could be obtained.
【0039】[0039]
【発明の効果】かくして、この発明によれば、高速溶接
時においても、ガスの発生を効果的に抑制して、耐ポッ
クマーク性に優れるだけでなく、良好な溶接作業性を有
するサブマージアーク溶接用の高温焼成型フラックスを
安定して得ることができる。Thus, according to the present invention, even during high-speed welding, the generation of gas is effectively suppressed, and the submerged arc welding not only has excellent pock mark resistance but also has good welding workability. High-temperature sintering type flux can be stably obtained.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 手塚 伸夫 千葉県千葉市中央区川崎町1番地 川崎製 鉄株式会社千葉製鉄所内 (72)発明者 西尾 要 千葉県千葉市中央区川崎町1番地 川崎製 鉄株式会社千葉製鉄所内 Fターム(参考) 4E084 AA03 AA06 AA07 AA11 CA16 DA18 ──────────────────────────────────────────────────続 き Continuing from the front page (72) Inventor Nobuo Tezuka 1 Kawasaki-cho, Chuo-ku, Chiba-shi, Chiba Chiba Works, Ltd. F term in Chiba Works (reference) 4E084 AA03 AA06 AA07 AA11 CA16 DA18
Claims (3)
750℃を超える温度で焼成してサブマージアーク溶接用
フラックスを製造するに際し、 700℃以上、(最高温度
−50℃)以下の温度域を5℃/min以上の昇温速度で昇温
し、焼成することを特徴とするサブマージアーク溶接用
焼成型フラックスの製造方法。Claims 1. A granulated powder of a calcined flux raw material,
When producing flux for submerged arc welding by firing at a temperature exceeding 750 ° C, the temperature range of 700 ° C or higher and (maximum temperature −50 ° C) or lower is raised at a rate of 5 ° C / min or higher, and firing is performed. A method for producing a fired flux for submerged arc welding.
クスの製造方法。2. The method of claim 1, the flux component, total SiO 2: 30 to 70 wt%, manganese oxide (in amount of MnO terms): 5~40wt%, MgO: 3~30wt %, A1 2 0 3: A method for producing a firing flux for submerged arc welding having a composition containing 2 to 20 wt%.
あって、かつ粒径:106μm 超が重量比率で10%以下、
粒径:45μm 未満が重量比率で50%以下の粒度分布を有
するFe−Si粒子を、1〜10wt%の割合で配合した焼成型
フラックス原料を、造粒後、750 ℃以上の温度で焼成を
施して成るサブマージアーク溶接用フラックスの製造方
法において、焼成に際し、 700℃以上、(最高温度−50
℃)以下の温度域を5℃/min以上の昇温速度で昇温する
ことを特徴とするサブマージアーク溶接用焼成型フラッ
クスの製造方法。3. A deoxidizing agent having a Si content of 30 to 80 wt% and a particle size of more than 106 μm in a weight ratio of 10% or less,
Particle size: Fe-Si particles having a particle size distribution of less than 45 μm with a weight ratio of 50% or less are blended at a ratio of 1 to 10% by weight. In the method for producing a flux for submerged arc welding, which is performed, at the time of firing, 700 ° C or more, (maximum temperature −50
A method for producing a fired flux for submerged arc welding, wherein the temperature is raised at a rate of 5 ° C./min or higher in a temperature range of not higher than 5 ° C.
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|---|---|---|---|
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14468699A JP3577995B2 (en) | 1999-05-25 | 1999-05-25 | Manufacturing method of fired flux for submerged arc welding |
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| Publication Number | Publication Date |
|---|---|
| JP2000334596A true JP2000334596A (en) | 2000-12-05 |
| JP3577995B2 JP3577995B2 (en) | 2004-10-20 |
Family
ID=15367909
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|---|---|---|---|
| JP14468699A Expired - Lifetime JP3577995B2 (en) | 1999-05-25 | 1999-05-25 | Manufacturing method of fired flux for submerged arc welding |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001038486A (en) * | 1999-07-29 | 2001-02-13 | Kawasaki Steel Corp | Sintered flux for submerged arc welding excellent in moisture absorption resistance and powdering resistance and method for producing the same |
| CN109926758A (en) * | 2018-11-03 | 2019-06-25 | 上海纪好旺造船科技发展有限公司 | A kind of Austenite and ferriteaustenite double phases of stainless steel submerged arc sintered flux and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107745203A (en) * | 2017-09-29 | 2018-03-02 | 四川西冶新材料股份有限公司 | Large-scale water power 800MPa level high-strength steel submerged arc fluxes and its production method |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6268695A (en) * | 1985-09-19 | 1987-03-28 | Nippon Steel Corp | High temperature calcined flux for submerged arc welding |
| JPS62240195A (en) * | 1986-04-11 | 1987-10-20 | Nippon Steel Corp | Low hydrogen type bond flux |
| JP2000288779A (en) * | 1999-01-29 | 2000-10-17 | Kawasaki Steel Corp | Fired flux for submerged arc welding |
| JP2001038486A (en) * | 1999-07-29 | 2001-02-13 | Kawasaki Steel Corp | Sintered flux for submerged arc welding excellent in moisture absorption resistance and powdering resistance and method for producing the same |
-
1999
- 1999-05-25 JP JP14468699A patent/JP3577995B2/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6268695A (en) * | 1985-09-19 | 1987-03-28 | Nippon Steel Corp | High temperature calcined flux for submerged arc welding |
| JPS62240195A (en) * | 1986-04-11 | 1987-10-20 | Nippon Steel Corp | Low hydrogen type bond flux |
| JP2000288779A (en) * | 1999-01-29 | 2000-10-17 | Kawasaki Steel Corp | Fired flux for submerged arc welding |
| JP2001038486A (en) * | 1999-07-29 | 2001-02-13 | Kawasaki Steel Corp | Sintered flux for submerged arc welding excellent in moisture absorption resistance and powdering resistance and method for producing the same |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001038486A (en) * | 1999-07-29 | 2001-02-13 | Kawasaki Steel Corp | Sintered flux for submerged arc welding excellent in moisture absorption resistance and powdering resistance and method for producing the same |
| CN109926758A (en) * | 2018-11-03 | 2019-06-25 | 上海纪好旺造船科技发展有限公司 | A kind of Austenite and ferriteaustenite double phases of stainless steel submerged arc sintered flux and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3577995B2 (en) | 2004-10-20 |
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