JPH054199B2 - - Google Patents
Info
- Publication number
- JPH054199B2 JPH054199B2 JP16501286A JP16501286A JPH054199B2 JP H054199 B2 JPH054199 B2 JP H054199B2 JP 16501286 A JP16501286 A JP 16501286A JP 16501286 A JP16501286 A JP 16501286A JP H054199 B2 JPH054199 B2 JP H054199B2
- Authority
- JP
- Japan
- Prior art keywords
- flux
- wire
- annealing
- moisture content
- hydrogen
- 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
Links
- 230000004907 flux Effects 0.000 claims description 39
- 238000000137 annealing Methods 0.000 claims description 22
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 230000001603 reducing effect Effects 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 19
- 239000001257 hydrogen Substances 0.000 description 19
- 229910052739 hydrogen Inorganic materials 0.000 description 19
- 229910052751 metal Inorganic materials 0.000 description 17
- 239000002184 metal Substances 0.000 description 17
- 238000012360 testing method Methods 0.000 description 14
- 238000011049 filling Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 238000003466 welding Methods 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 239000007789 gas Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000000605 extraction Methods 0.000 description 5
- 239000011261 inert gas Substances 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- 239000003921 oil Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910000765 intermetallic Inorganic materials 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- 238000005491 wire drawing Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000004455 differential thermal analysis Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 230000035553 feeding performance Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000004021 metal welding Methods 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
Landscapes
- Nonmetallic Welding Materials (AREA)
Description
[産業上の利用分野]
本発明はフラツクス中に含有されている金属成
分や金属間化合物が、ワイヤ焼鈍時に酸化される
ことのない継目なしフラツクス入りワイヤの製造
方法に関するものである。
[従来の技術]
金属の溶接において溶接金属中に拡散性水素が
存在すると被溶接物の耐割れ性や耐気孔性を損な
うおそれがある。このため溶接金属中の拡散性水
素量を抑制する手段の1つとして溶接ワイヤに充
填されるフラツクスについては可能な限りポテン
シヤル水分量を減らすことが要請される。そこで
従来のフラツクス入りワイヤの製造においては、
十分乾燥させてポテンシヤル水分量を10〜70ppm
程度にしたフラツクスを充填することが必要とさ
れていた。
尚本明細書においてポテンシヤル水分とは、水
分のみならず、油類その他のあらゆる水素源を含
む全てのものである。ところで継目なしフラツク
ス入りワイヤは、ワイヤの送給性を改善すること
を主目的に開発されたものであり、その製造に当
たつては、引抜管、押出管或は溶接管等のパイプ
に十分乾いたフラツクスを充填した後、若しくは
帯板にフラツクスを散布しながら該帯板を巻き込
んでシームを溶接し、次いで伸線及びめつきの各
工程を経ることにより行なわれるが、伸線工程の
前・中・後いずれかにおいて焼鈍工程に付加する
のが一般であり、これによりワイヤの硬度が低下
されかつ均一になる。
[発明が解決しようとする問題点]
上記のようにポテンシヤル水分量を十分に抑制
した乾燥性フラツクスを使用した場合でも、500
℃以上で焼鈍を実施すると、フラツクスに添加さ
れているMgやAl等の金属成分及びこれらの金属
間化合物がきわめて容易に酸化され、その添加目
的であるアーク安定性、脱酸性を著しく損なうと
いう問題を招来する。示差熱分析による調査の結
果では、フラツクス中の例えばMg及びAlは、焼
鈍温度が550℃を越えるといずれも酸化しはじめ
ることが分かつている。そこで本発明者等は、フ
ラツクス充填部をAr及びN2ガスで置換すること
により不活性ガス雰囲気にした状態で該フラツク
ス中のMg及びAlの酸化調査を行なつた。その結
果、いずれの不活性ガスの場合も、Mg及びAlの
酸化が進行していて、フラツクス中の添加金属の
酸化防止は不十分であることがわかつた。これら
のことから本発明者等は、ワイヤ焼鈍時における
添加金属の酸化を防止するには、ワイヤ焼鈍時に
おけるフラツクス充填部の雰囲気を単に不活性雰
囲気とするのではなく思い切つて還元雰囲気にす
る必要があるのではないかとの指針を得るに至つ
た。
本発明はこの様な事情に鑑みてなされたもので
あつて、その目的はワイヤ焼鈍時にフラツクス充
填部に強い還元雰囲気を形成することによつて、
添加金属の酸化を防止し、しかも溶接金属中の拡
散性水素の抑制を可能ならしめる継目なしフラツ
クス入りワイヤの製造方法を提供することにあ
る。
[問題点を解決するための手段]
本発明に係る継目なしフラツクス入りワイヤの
製造方法は、焼鈍前におけるワイヤのポテンシヤ
ル水分量を80〜3000ppmに調整し、ワイヤを焼鈍
したときに原子状水素を発生させることによりフ
ラツクス充填部に還元雰囲気を形成する点にその
要旨を有するものである。
[作用]
フラツクス充填部に還元雰囲気を形成する方法
としては、フラツクス充填部をH2ガスで置換す
る方法も考えられるが、この方法で導入された
H2は、ワイヤ焼鈍後もフラツクス充填部にH2ガ
スとしてそのまま滞留するので、溶接金属中の拡
散性水素量が増大するという問題が生じる。とこ
ろが原子状水素で還元雰囲気を形成すれば原子状
水素はH2ガスよりも還元性がはるかに強く、し
かも元々拡散性に富んでいる為、焼鈍後冷却され
る迄の間にパイプ壁を通して外部に散逸され易い
という特性があり、原子状水素がワイヤ中に多量
に残存することはないのである。即ち焼鈍時はパ
イプ内にあつてAl等の酸化を防止し、焼鈍後は
速やかに放散されるという誠に好都合な成分であ
る。尚原子状水素は極めて不安定であるから焼鈍
前からワイヤ内部に添加しておくことは困難であ
る。このため本発明においては、焼鈍により原子
状水素をフラツクス充填部に発生させる構成とし
たものである。原子状水素は、ワイヤのポテンシ
ヤル水分量を適宜制御すれば、焼鈍時の加熱によ
り、下記の又はの反応機構にしたがつて生成
する。
フラツクス被添加金属+H2O
加熱
――→
金属酸化物+H(原子状水素)
有機物熱分解
―――→
H2O+低級炭化水素+H(原子状水素)
本発明者等はの反応に関し、フラツクス被添
加金属の1つである鉄粉について検討・分析した
結果、の反応は180℃前後から始まり、600℃に
おいては水分の約80%が原子状水素になつている
ことをガスクロマトグラフイーにより確認した。
の反応は、主としてフラツクス充填部のパイ
プ類に付着している油や油脂類等のポテンシヤル
水分量の熱分解であるが、これらは溶接金属中の
拡散性水素源として、従来は有機溶剤などを用い
て除去していたものである。
この様に従来技術においてはフラツクスへの添
加を可能な限り抑制していた水分,油等の水素源
を、本発明においては逆に積極的に添加して前記
した本発明の目的を達成せんとするものである。
ワイヤのポテンシヤル水分量は80〜3000ppm、
好ましくは100〜1000ppmに調整する。
ワイヤのポテンシヤル水分量が80ppm未満の場
合、焼鈍に際して生成する水分量が少ないので
MgやAl等の被溶加金属の酸化を防止することが
できない。一方ワイヤのポテンシヤル水分量が
3000ppmを超えると、前記,の反応に関与し
なかつた水分が製品中に残存し溶接金属中の拡散
性水素量を増大させる。
[実施例]
以下、本発明を実施例により更に具体的に説明
するが、本発明はこれらの実施例に限定されるも
のではない。
尚本発明においてはワイヤのポテンシヤル水分
量の測定方法は、特に限定されるものではない
が、以下の実施例ではカールフイツシヤー法及び
不活性ガス抽出法を用いた。焼鈍前の供試ワイヤ
の表面をエーテル等の有機溶媒を用いて洗浄した
あと、カールフイツシヤー法は酸素雰囲気中で
750〜1000℃で抽出して水分量を定量するもので
あり、不活性ガス抽出法はワイヤ中に含まれる水
素源を炭素と反応させることにより還元し、生成
した水素量をガスクロマトグラフにより定量し
て、その数値を水分量に換算するものである。
フラツクス入りワイヤは軟鋼製パイプにフラツ
クスを充填し、常法に従つてワイヤ径1.2mm〓のも
のを製造した。
第1表に軟鋼製パイプの成分組成を重量%で示
す。また第2表にフラツクス組成の配合量を重量
%で示す。
[Industrial Field of Application] The present invention relates to a method for producing a seamless flux-cored wire in which metal components and intermetallic compounds contained in the flux are not oxidized during wire annealing. [Prior Art] When diffusible hydrogen is present in the weld metal during welding of metals, there is a risk that the cracking resistance and porosity resistance of the welded object may be impaired. Therefore, as one means for suppressing the amount of diffusible hydrogen in the weld metal, it is required to reduce the potential moisture content of the flux filled into the welding wire as much as possible. Therefore, in the production of conventional flux-cored wire,
Dry thoroughly to reduce the potential moisture content to 10 to 70 ppm.
It was necessary to fill with a certain amount of flux. In this specification, potential moisture includes not only moisture but also oils and all other hydrogen sources. By the way, seamless flux-cored wire was developed with the main purpose of improving the wire feeding performance, and when manufacturing it, it is necessary to make sure that it is suitable for pipes such as drawn pipes, extruded pipes, welded pipes, etc. This is done by filling the strip with dry flux or by sprinkling flux on the strip, rolling the strip and welding the seam, and then going through the wire drawing and plating steps, but before the wire drawing step. It is generally added during or after the annealing process to reduce and make the hardness of the wire uniform. [Problems to be solved by the invention] Even when a drying flux with sufficiently suppressed potential moisture content is used as described above, 500%
When annealing is carried out at temperatures above ℃, the metal components such as Mg and Al added to the flux and their intermetallic compounds are extremely easily oxidized, which significantly impairs arc stability and deoxidizing properties, which are the purpose of their addition. invite. As a result of investigation by differential thermal analysis, it has been found that, for example, Mg and Al in the flux begin to oxidize when the annealing temperature exceeds 550°C. Therefore, the present inventors conducted an investigation on the oxidation of Mg and Al in the flux in an inert gas atmosphere by replacing the flux filling part with Ar and N2 gas. As a result, it was found that oxidation of Mg and Al progressed in all cases of inert gas, and that the oxidation prevention of added metals in the flux was insufficient. Based on these facts, the present inventors have determined that in order to prevent the oxidation of the added metal during wire annealing, the atmosphere in the flux-filled part during wire annealing should not be simply an inert atmosphere, but a reducing atmosphere. I have come to the conclusion that this may be necessary. The present invention has been made in view of the above circumstances, and its purpose is to form a strong reducing atmosphere in the flux-filled part during wire annealing.
It is an object of the present invention to provide a method for producing a seamless flux-cored wire that prevents oxidation of additive metals and suppresses diffusible hydrogen in weld metal. [Means for Solving the Problems] The method for producing a seamless flux-cored wire according to the present invention is to adjust the potential water content of the wire to 80 to 3000 ppm before annealing, and to release atomic hydrogen when the wire is annealed. The gist is that a reducing atmosphere is formed in the flux filling section by generating the flux. [Function] As a method of forming a reducing atmosphere in the flux-filled part, it is possible to replace the flux-filled part with H 2 gas.
Since H 2 remains in the flux-filled portion as H 2 gas even after wire annealing, a problem arises in that the amount of diffusible hydrogen in the weld metal increases. However, if a reducing atmosphere is formed using atomic hydrogen, atomic hydrogen has a much stronger reducing property than H 2 gas, and since it is inherently highly diffusive, it can pass through the pipe wall to the outside after annealing and before it is cooled. Atomic hydrogen has the property of being easily dissipated, so that a large amount of atomic hydrogen does not remain in the wire. That is, it is a truly advantageous component that is present in the pipe during annealing and prevents the oxidation of Al, etc., and is quickly dissipated after annealing. Since atomic hydrogen is extremely unstable, it is difficult to add it to the inside of the wire before annealing. Therefore, in the present invention, atomic hydrogen is generated in the flux-filled portion by annealing. If the potential water content of the wire is appropriately controlled, atomic hydrogen is generated by heating during annealing according to the following reaction mechanism. Flux-added metal + H 2 O Heating -> Metal oxide + H (atomic hydrogen) Organic matter thermal decomposition - -> H 2 O + lower hydrocarbon + H (atomic hydrogen) As a result of studying and analyzing iron powder, which is one of the additive metals, it was confirmed by gas chromatography that the reaction starts at around 180℃, and at 600℃, about 80% of the water becomes atomic hydrogen. . The reaction is mainly the thermal decomposition of the potential moisture content of oil and fats adhering to the pipes in the flux filling section, but these reactions have traditionally been treated using organic solvents as sources of diffusible hydrogen in the weld metal. It was used to remove it. In this way, in the prior art, the addition of hydrogen sources such as water and oil to the flux was suppressed as much as possible, but in the present invention, on the contrary, it is actively added to achieve the above-mentioned object of the present invention. It is something to do. The potential moisture content of the wire is 80~3000ppm,
Preferably it is adjusted to 100 to 1000 ppm. If the potential moisture content of the wire is less than 80ppm, the amount of moisture generated during annealing is small.
Oxidation of filler metals such as Mg and Al cannot be prevented. On the other hand, the potential moisture content of the wire is
If it exceeds 3000 ppm, water that did not participate in the above reaction will remain in the product, increasing the amount of diffusible hydrogen in the weld metal. [Examples] Hereinafter, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to these Examples. In the present invention, the method for measuring the potential water content of the wire is not particularly limited, but in the following examples, the Karl Fischer method and the inert gas extraction method were used. After cleaning the surface of the test wire before annealing using an organic solvent such as ether, the Karl Fischer method is performed in an oxygen atmosphere.
The amount of water is determined by extraction at 750 to 1000℃, and the inert gas extraction method reduces the hydrogen source contained in the wire by reacting with carbon, and the amount of hydrogen produced is determined using a gas chromatograph. This value is then converted into water content. The flux-cored wire was manufactured by filling a mild steel pipe with flux and using a conventional method to produce a wire with a diameter of 1.2 mm. Table 1 shows the composition of the mild steel pipe in weight percent. Table 2 also shows the amount of the flux composition in weight percent.
【表】【table】
【表】
<ポテンシヤル水分量の制御>
ワイヤのポテンシヤル水分量の制御は充填され
るフラツクスを吸湿させる方法により行なつた。
<アーク安定性の判定>
アーク安定性の調査はアークの強さ、広がりの
変動、アークのばたつき、ワイヤの突出長さの変
動、スパツタ及びヒユーム発生量を総合して行な
つた。尚、以下の各表中、○:良好、△:やや不
良、×:不良を夫々あらわす。
<拡散性水素量の測定>
ガスクロマトグラフ法により測定した。
実施例 1
第1表A−1に示す組成のパイプに第2表B−
1に示す組成のフラツクスを充填して、フラツク
ス入りワイヤを製造した。ワイヤに対するフラツ
クスの充填率は14%とした。焼鈍前ワイヤの水分
量(ppm)の測定は、カールフイツシヤー法(酸
素雰囲気、750℃抽出)により行なつた。溶接は
次の条件下で行なつた。
<溶接条件>
電源:直流・逆極性
電流:250A
電圧:27〜28V
姿勢:下向
速度:30cm/分
シールドガス:100%CO2 25/分
試験板:SM50A
尚、数値は少数点以下を四捨五入した値であ
る。試験結果を第3表に示す。[Table] <Control of Potential Moisture Content> The potential moisture content of the wire was controlled by a method in which the flux to be filled was made to absorb moisture. <Determination of Arc Stability> Arc stability was investigated by comprehensively examining arc strength, variation in spread, arc flapping, variation in wire protrusion length, and amount of spatter and fume generation. In the following tables, ◯: good, △: slightly poor, ×: poor, respectively. <Measurement of diffusible hydrogen amount> Measured by gas chromatography. Example 1 A pipe with the composition shown in Table 1 A-1 was combined with the composition shown in Table 2 B-
A flux-cored wire was manufactured by filling the wire with a flux having the composition shown in 1. The flux filling rate for the wire was 14%. The moisture content (ppm) of the wire before annealing was measured by the Karl Fischer method (oxygen atmosphere, extraction at 750°C). Welding was performed under the following conditions. <Welding conditions> Power source: DC/reverse polarity Current: 250A Voltage: 27~28V Posture: Downward Speed: 30cm/min Shielding gas: 100% CO 2 25/min Test plate: SM50A Note that numbers are rounded to the nearest whole decimal place. This is the value. The test results are shown in Table 3.
【表】【table】
【表】
第3表から明らかな様に、
試験番号1及び2のものはワイヤの水分量が少
ないためフラツクス中のMgが酸化され、その結
果アーク安定性の悪化が観察された。
試験番号9及び10のものは、ワイヤの水分量過
多のため拡散性水素量が大となり、またアーク安
定性もやや劣化した。
試験番号3〜8のものは、本発明の条件を全く
満たすものであつて、いずれもアーク安定性が良
好であり且つ拡散性水素量も低水準であつた。
実施例 2
第1表A−2に示す組成のパイプに第2表B−
2に示す組成のフラツクスを充填して、フラツク
ス入りワイヤを製造した。ワイヤに対するフラツ
クスの充填率は15%とした。焼鈍前ワイヤの水分
量の測定は実施例1の場合と同じとした。また、
溶接電流量は280Aとし、他の溶接条件は実施例
1の場合と同じとした。
試験結果を第4表に示す。[Table] As is clear from Table 3, in test numbers 1 and 2, Mg in the flux was oxidized due to the low moisture content of the wires, and as a result, deterioration of arc stability was observed. In test numbers 9 and 10, the amount of diffusible hydrogen was large due to excessive moisture content in the wire, and the arc stability was also slightly degraded. Test Nos. 3 to 8 completely satisfied the conditions of the present invention, and all had good arc stability and a low amount of diffusible hydrogen. Example 2 A pipe with the composition shown in Table 1 A-2 and Table 2 B-
A flux-cored wire was manufactured by filling the wire with a flux having the composition shown in 2. The flux filling rate for the wire was 15%. The measurement of the moisture content of the wire before annealing was the same as in Example 1. Also,
The amount of welding current was 280A, and other welding conditions were the same as in Example 1. The test results are shown in Table 4.
【表】
第4表から明らかな様に、
試験番号1のものはワイヤの水分量が少ないた
めフラツクス中のMg合金粉が酸化され、その結
果アーク安定性の悪化が観察された。
試験番号10のものはワイヤの水分量過多のため
拡散性水素量が大となり、またアークの安定性も
やや劣化した。
試験番号2〜9のものは、本発明の条件を全て
満たすものであつて、いずれもアーク安定性が良
好であり、且つ拡散性水素量も低水準であつた。
実施例 3
第1表A−1に示す組成のパイプに第2表B−
3に示す組成のフラツクスを充填して、フラツク
ス入りワイヤを製造した。ワイヤに対するフラツ
クスの充填率は12%とした。焼鈍前ワイヤの水分
量の測定は前記不活性ガス抽出法により行なつ
た。また溶接条件は実施例2と同じとした。
試験結果を第5表に示す。[Table] As is clear from Table 4, in test number 1, the Mg alloy powder in the flux was oxidized due to the low moisture content of the wire, and as a result, deterioration of arc stability was observed. In test number 10, the amount of diffusible hydrogen was large due to excessive moisture content in the wire, and the stability of the arc was also slightly degraded. Test Nos. 2 to 9 satisfied all the conditions of the present invention, and all had good arc stability and a low amount of diffusible hydrogen. Example 3 A pipe with the composition shown in Table 1 A-1 was combined with Table 2 B-
A flux-cored wire was manufactured by filling the wire with a flux having the composition shown in No. 3. The flux filling rate for the wire was 12%. The moisture content of the wire before annealing was measured by the inert gas extraction method described above. Further, the welding conditions were the same as in Example 2. The test results are shown in Table 5.
【表】
第5表から明らかな様に、
試験番号1のものはワイヤの水分量が少ないた
め、フラツクス中のA1粉が酸化され、その結果
アーク安定性の悪化が観察された。
試験番号8のものは、ワイヤの水分量過多のた
め拡散性水素量が大となり、アーク安定性もやや
劣化した。
試験番号2〜7のものは、本発明の条件を全て
満たすものであつて、いずれもアーク安定性が良
好であり、且つ拡散性の水素量も低水準であつ
た。
[発明の効果]
本発明に係るフラツクス入りワイヤの製造方法
によれば、従来技術ではフラツクスに添加するこ
とを可能な限り抑制すべきものとされていた水
分、油類等の水素源を、フラツクス中に逆に積極
的に添加することによつて、ワイヤ製造途次にお
ける焼鈍工程においても、フラツクス中の被添加
金属が酸化されることを防止したものである。従
つて上記被添加金属はその添加目的であるアーク
安定剤及び脱酸剤としての機能を十分に発揮し、
しかも溶接金属中の拡散性水素量が低水準に抑制
される効果と相俟つてすぐれた溶接作業性を示す
継目なしフラツクス入りワイヤが得られるのであ
る。[Table] As is clear from Table 5, in test number 1, because the moisture content of the wire was small, the A1 powder in the flux was oxidized, and as a result, deterioration of arc stability was observed. In test number 8, the amount of diffusible hydrogen was large due to the excessive moisture content of the wire, and the arc stability was also slightly deteriorated. Test Nos. 2 to 7 satisfied all the conditions of the present invention, had good arc stability, and had a low amount of diffusible hydrogen. [Effects of the Invention] According to the method for producing a flux-cored wire according to the present invention, hydrogen sources such as moisture and oil, which should be suppressed as much as possible from being added to flux in the conventional technology, can be added to the flux. On the contrary, by actively adding the flux to the flux, it is possible to prevent the added metal in the flux from being oxidized even during the annealing process during wire manufacturing. Therefore, the above-mentioned additive metals sufficiently perform their functions as arc stabilizers and deoxidizers, which are the purposes for which they are added.
Moreover, in combination with the effect of suppressing the amount of diffusible hydrogen in the weld metal to a low level, a seamless flux-cored wire exhibiting excellent welding workability can be obtained.
Claims (1)
を80〜3000ppmに調整し、ワイヤを焼鈍して原子
状水素を発生させることによりフラツクス充填部
に還元雰囲気を形成することを特徴とする継目な
しフラツクス入りワイヤの製造方法。1. A seamless flux-cored wire characterized in that the potential water content of the wire before annealing is adjusted to 80 to 3000 ppm, and the wire is annealed to generate atomic hydrogen to form a reducing atmosphere in the flux-filled part. Production method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16501286A JPS6320198A (en) | 1986-07-14 | 1986-07-14 | Production of seamless flux cored wire |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16501286A JPS6320198A (en) | 1986-07-14 | 1986-07-14 | Production of seamless flux cored wire |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6320198A JPS6320198A (en) | 1988-01-27 |
| JPH054199B2 true JPH054199B2 (en) | 1993-01-19 |
Family
ID=15804164
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16501286A Granted JPS6320198A (en) | 1986-07-14 | 1986-07-14 | Production of seamless flux cored wire |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6320198A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102513549A (en) * | 2011-12-22 | 2012-06-27 | 中国南方航空工业(集团)有限公司 | Method for processing eccentric inner hole |
-
1986
- 1986-07-14 JP JP16501286A patent/JPS6320198A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102513549A (en) * | 2011-12-22 | 2012-06-27 | 中国南方航空工业(集团)有限公司 | Method for processing eccentric inner hole |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6320198A (en) | 1988-01-27 |
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