CN1102480C - Process for manufacturing welding wire - Google Patents
Process for manufacturing welding wire Download PDFInfo
- Publication number
- CN1102480C CN1102480C CN97102700A CN97102700A CN1102480C CN 1102480 C CN1102480 C CN 1102480C CN 97102700 A CN97102700 A CN 97102700A CN 97102700 A CN97102700 A CN 97102700A CN 1102480 C CN1102480 C CN 1102480C
- Authority
- CN
- China
- Prior art keywords
- wire
- flux
- welding wire
- diameter
- temperature
- 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 - Fee Related
Links
- 238000003466 welding Methods 0.000 title claims abstract description 109
- 238000000034 method Methods 0.000 title claims abstract description 32
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 15
- 230000004907 flux Effects 0.000 claims abstract description 73
- 238000010438 heat treatment Methods 0.000 claims abstract description 61
- 239000002184 metal Substances 0.000 claims abstract description 29
- 229910052751 metal Inorganic materials 0.000 claims abstract description 29
- 239000001257 hydrogen Substances 0.000 abstract description 53
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 53
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 42
- 238000006356 dehydrogenation reaction Methods 0.000 abstract description 30
- 229910000831 Steel Inorganic materials 0.000 abstract description 13
- 239000010959 steel Substances 0.000 abstract description 13
- 238000011282 treatment Methods 0.000 abstract description 12
- 238000005485 electric heating Methods 0.000 abstract description 9
- 210000003491 skin Anatomy 0.000 description 63
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 238000001816 cooling Methods 0.000 description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 238000000137 annealing Methods 0.000 description 6
- 150000002431 hydrogen Chemical class 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 238000004381 surface treatment Methods 0.000 description 5
- 239000000945 filler Substances 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000004817 gas chromatography Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000010943 off-gassing Methods 0.000 description 3
- 238000005452 bending Methods 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910000976 Electrical steel Inorganic materials 0.000 description 1
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 1
- 229910000746 Structural steel Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000005112 continuous flow technique Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 230000035553 feeding performance Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000005482 strain hardening Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
Landscapes
- Nonmetallic Welding Materials (AREA)
- Heat Treatment Of Strip Materials And Filament Materials (AREA)
Abstract
一种用来制造直径0.8至4mm的、具有优异的抗裂缝力和底层涂料防护质量并含有非常少的扩散氢的、适合于焊接高强度钢和承受大约束力的钢结构的无缝药芯焊丝,通过用高温加热进行脱氢处理来制造的工艺包括步骤:通过经布置成相隔2至5m的第一和第二对辊电极并经布置在它们之间的环心变压器的直接电加热,把直径8至15mm的直焊丝加热到620与1100℃之间的温度;用不高于250kcal/m2h℃(≈214.98W/(m2·K))的传热系数把已加热焊丝冷却到不高于500℃;以及拉伸到想要的直径。这样得到的焊丝形成的焊件每100g熔敷金属含有不超过5ml的扩散氢。
A seamless flux core suitable for welding high strength steel and steel structures subject to high restraints, with a diameter of 0.8 to 4mm, which has excellent crack resistance and primer protection qualities and contains very little diffusible hydrogen Welding wire, the process of manufacturing by dehydrogenation treatment with high temperature heating includes the steps of: by direct electric heating through first and second pair of roller electrodes arranged at a distance of 2 to 5 m and through a toroidal transformer arranged between them, Heat a straight welding wire with a diameter of 8 to 15mm to a temperature between 620 and 1100°C; cool the heated wire with a heat transfer coefficient not higher than 250kcal/m 2 h°C (≈214.98W/(m 2 ·K)) to no higher than 500°C; and stretched to the desired diameter. The weldment formed from the wire thus obtained contains not more than 5ml of diffusible hydrogen per 100g of deposited metal.
Description
本发明涉及一种制造低氢焊接用药芯焊丝的工艺,该焊丝具有很高的抗裂缝力和底层涂料防护质量,适合用于高强度钢和其他优质钢的焊接和承受大约束力的钢结构。The invention relates to a process for manufacturing flux-cored welding wire for low-hydrogen welding. The welding wire has high crack resistance and primer protection quality, and is suitable for welding high-strength steel and other high-quality steels and steel structures that withstand large binding forces .
无缝药芯焊丝制造工艺中的脱氢处理一般按如下方法进行:在钟式炉或隧道式拱炉中把由直径10至13mm拉伸至2至4mm的管材药芯焊丝加热到600至800℃。加热脱氢处理由于以下理由而用于2至4mm的小直径焊丝:(1)尚没有对较大直径焊丝的有效的加热脱氢处理工艺;以及(2)小直径焊丝容易弄成螺圈或环形,这是缩短钟式炉或隧道式拱炉的总长度所需要的。The dehydrogenation treatment in the seamless flux-cored wire manufacturing process is generally carried out as follows: heat the tubular flux-cored wire stretched from 10 to 13 mm in diameter to 2 to 4 mm in a bell furnace or tunnel arch furnace to 600 to 800 ℃. Heat dehydrogenation is used for small diameter wires from 2 to 4 mm for the following reasons: (1) there is no effective heat dehydrogenation process for larger diameter wires; and (2) small diameter wires tend to coil or Ring, which is required to shorten the overall length of bell furnaces or tunnel arch furnaces.
此外,必须控制表皮的硬度以满足各个药芯焊丝的填充比和其他技术条件,从而在自动焊接期间保证0.8到4mm直径焊丝的良好送丝效率并在制造期间防止焊丝的断裂。于是,将要加热的焊丝的直径必须通过考虑表皮的冷作硬化来确定,当焊丝在软化退火之后受到拉伸时会出现这种表皮冷作硬化。这样,进行一次加热可以服务于两种不同的目的,即脱氢和表皮的软化。此外,常用的钟式炉和隧道式拱炉并不完全令人满意,因为钟式炉的生产率低而隧道式拱炉的热效率低,隧道式拱炉的材料、结构和使用寿命不允许在高于800℃的温度下使用并且它们需要大安装空间。In addition, the hardness of the skin must be controlled to meet the filling ratio and other technical conditions of each flux-cored wire, so as to ensure good wire feeding efficiency of 0.8 to 4mm diameter wire during automatic welding and prevent wire breakage during manufacturing. Then, the diameter of the welding wire to be heated must be determined by taking into account the work hardening of the skin which occurs when the welding wire is stretched after softening annealing. Thus, one heating can serve two different purposes, dehydrogenation and softening of the skin. In addition, the commonly used bell furnace and tunnel arch furnace are not completely satisfactory, because the productivity of the bell furnace is low and the thermal efficiency of the tunnel arch furnace is low, and the material, structure and service life of the tunnel arch furnace do not allow high Used at temperatures of 800°C and they require a large installation space.
随着自动焊接已变得普及,裸焊丝、药芯焊丝的使用也已增加,同时带有缝表皮的药芯焊丝构成主流。由于100g熔敷金属产生大约7ml的扩散氢,所以这种焊丝有一种讨厌的倾向,即在高强度钢的焊接中或在承受大约束力的钢结构中形成氢诱发裂缝。当用来焊接带底层涂料的钢板时,含氢过多的焊丝具有形成气隙、缩孔和其他焊接缺陷的倾向。As automatic welding has become popular, the use of bare wire and flux-cored wire has also increased, while flux-cored wire with seam skins constitutes the mainstream. Since 100g of deposited metal produces approximately 7ml of diffusible hydrogen, this wire has an undesirable tendency to form hydrogen-induced cracks in welding of high strength steels or in steel structures subjected to high restraint forces. When used to weld primed steel, wires containing too much hydrogen have a tendency to form air voids, shrinkage cavities, and other weld defects.
之所以难于制造带有缝表皮的低氢焊丝的原因如下:(1)所填充焊剂含有粘合水分;(2)除非加热到500℃以上,无法从填充焊剂所含的某些无机物中去除结晶水;(3)填充焊剂所含的某些金属粉末含有除非加热到300℃以上就无法去除的氢;(4)当加热到高温时,经表皮缝隙进入的氧通过加速氧化而使填充焊剂质量劣化;以及(5)经表皮缝隙的沾湿使得无法制造低氢药芯焊丝。The reason why it is difficult to manufacture a low-hydrogen welding wire with a seam skin is as follows: (1) The filled flux contains binding moisture; (2) It cannot be removed from certain inorganic substances contained in the filled flux unless it is heated above 500°C Crystal water; (3) Certain metal powders contained in the filler flux contain hydrogen that cannot be removed unless heated above 300°C; (4) When heated to high temperatures, the oxygen that enters through the skin gaps accelerates the oxidation to make the filler flux Quality deterioration; and (5) Wetting through skin crevices makes it impossible to manufacture low-hydrogen flux-cored wires.
因而,开发了无缝药芯焊丝以便能制造低氢药芯焊丝。这种类型的低氢药芯焊丝通过往钢管中填充焊剂来制造。填充了的钢管被加热到600与800℃之间的温度以便脱氢。所填充焊剂中的水靠下面给出的化学反应变成原子氢并经表皮扩散。Thus, seamless flux-cored wires have been developed in order to be able to manufacture low-hydrogen flux-cored wires. This type of low hydrogen flux cored wire is manufactured by filling a steel pipe with flux. The filled steel pipe is heated to a temperature between 600 and 800°C for dehydrogenation. The water in the filled flux is converted to atomic hydrogen by the chemical reaction given below and diffuses through the skin.
式中Me:焊剂和表皮内壁中的还原剂或其他金属成分In the formula, Me: reducing agent or other metal components in the flux and the inner wall of the epidermis
H2O=所填充焊剂中的水H 2 O = water in filled flux
为了减少水和其他氢源(潜在氢),必须把焊丝加热到较高温度。另一方面,为了得到良好的送丝性能,必须适当地控制表皮软化退火的条件。然而,用一次加热的常规工艺不能提供带有经满意地脱氢处理的焊剂和经满意地软化处理的表皮的焊丝。进行较强的脱氢处理造成表皮的过度软化,根据焊丝规格的不同,这可能损害焊接期间的送丝。以较低一些的温度对表皮硬度适当的焊丝进行软化退火会造成脱氢不足,扩散氢数量增加,以及焊接金属抗裂缝力降低。常规的加热工艺不能满足对含氢量较低的焊丝和对较高的送丝速度的日益提高的要求。To reduce water and other sources of hydrogen (potential hydrogen), the wire must be heated to a higher temperature. On the other hand, in order to obtain good wire feeding performance, the conditions of skin softening annealing must be properly controlled. However, the conventional process with one heat does not provide a welding wire with a satisfactorily dehydrogenated flux and a satisfactorily softened skin. Doing a strong dehydrogenation treatment causes excessive softening of the skin which, depending on the wire gauge, can impair wire feed during welding. Soft annealing of wires with adequate skin hardness at lower temperatures will result in insufficient dehydrogenation, increased amounts of diffusible hydrogen, and reduced crack resistance of the weld metal. Conventional heating processes cannot meet the increasing demands for welding wires with lower hydrogen content and for higher wire feed speeds.
为了解决上述问题,发明人提供一种制造焊丝的新工艺,该工艺允许较强的脱氢处理并提供最佳的送丝速度,办法是对脱氢及表皮软化两道加热工序进行加热优化,而不是常规的一次加热。本发明的主要特征如下:In order to solve the above problems, the inventors provide a new process for manufacturing welding wire, which allows a strong dehydrogenation treatment and provides an optimal wire feed speed, by optimizing the heating of the two heating processes of dehydrogenation and skin softening, Instead of conventional one-time heating. Main features of the present invention are as follows:
(1)一种用高温加热来脱氢的无缝药芯焊丝制造工艺,该工艺包括步骤:以620与1100℃之间的温度直接电加热直焊丝,该直焊丝是用焊剂填充的金属管并有8至15mm的直径,通过令该焊丝穿过沿该焊丝走行路径相隔2至5m布置的第一和第二对辊电极并穿过布置在该两对辊电极之间的环心变压器中的开口来加热;用250kcal/m2h℃(≈214.98W/(m2·K),下同)以下的传热系数把所加热的焊丝冷却到500℃以下;以及把所冷却的焊丝拉伸到0.8和4mm之间的直径。(1) A process for manufacturing a seamless flux-cored wire for dehydrogenation by high-temperature heating, the process comprising the steps of: directly electrically heating a straight welding wire, which is a metal tube filled with flux, at a temperature between 620 and 1100°C and have a diameter of 8 to 15 mm, by passing the welding wire through the first and second pair of roller electrodes arranged at a distance of 2 to 5 m along the path of the welding wire and passing through the toroidal transformer arranged between the two pairs of roller electrodes to heat the opening; cool the heated wire to below 500°C with a heat transfer coefficient below 250kcal/m 2 h°C (≈214.98W/(m 2 ·K), the same below); and pull the cooled wire Extend to a diameter between 0.8 and 4mm.
(2)一种用高温加热来脱氢的无缝药芯焊丝制造工艺,该工艺包括步骤:以620与1100℃之间的温度直接电加热直焊丝,该直焊丝是用焊剂填充的金属管并有8至15mm的直径,通过令该焊丝穿过沿该焊丝走行路径相隔2至5m布置的第一和第二对辊电极并穿过布置在该两对辊电极之间的环心变压器中的开口来加热;在煤气加热炉或电加热炉中把预热的焊丝加热到600与800℃之间的温度用250kcal/m2h℃以下的传热系数把所加热的焊丝冷却到500℃以下;以及把所冷却的焊丝拉伸到0.8和4mm之间的直径。(2) A process for manufacturing a seamless flux-cored wire that uses high-temperature heating for dehydrogenation, the process comprising the steps of: directly electrically heating a straight welding wire, which is a metal tube filled with flux, at a temperature between 620 and 1100°C and have a diameter of 8 to 15 mm, by passing the welding wire through the first and second pair of roller electrodes arranged at a distance of 2 to 5 m along the path of the welding wire and passing through the toroidal transformer arranged between the two pairs of roller electrodes Heating through openings; heat the preheated welding wire to a temperature between 600 and 800°C in a gas heating furnace or an electric heating furnace, and cool the heated welding wire to 500°C with a heat transfer coefficient below 250kcal/m 2 h°C below; and drawing the cooled wire to a diameter between 0.8 and 4mm.
(3)一种用高温加热来脱氢的无缝药芯焊丝制造工艺,该工艺包括步骤:以620与1100℃之间的温度直接电加热直焊丝,该直焊丝是用焊剂填充的金属管并有8至15mm的直径,通过令该焊丝穿过沿该焊丝走行路径相隔2至5m布置的第一和第二对辊电极并穿过布置在该两对辊电极之间的环心变压器中的开口来加热;用250kcal/m2h℃以下的传热系数把所加热的焊丝冷却到500℃以下;把所冷却的焊丝拉伸到2和7mm之间的直径;在煤气加热炉或电加热炉中把已拉伸的焊丝加热到600与800℃之间的温度;用250kcal/m2h℃以下的传热系数把所加热的焊丝冷却到500℃以下;以及把所冷却的焊丝拉伸到0.8与4mm之间的直径。(3) A process for manufacturing a seamless flux-cored wire for dehydrogenation by high-temperature heating, the process comprising the steps of: directly electrically heating a straight welding wire, which is a metal tube filled with flux, at a temperature between 620 and 1100°C and have a diameter of 8 to 15 mm, by passing the welding wire through the first and second pair of roller electrodes arranged at a distance of 2 to 5 m along the path of the welding wire and passing through the toroidal transformer arranged between the two pairs of roller electrodes Heating through openings; cooling the heated wire to below 500°C with a heat transfer coefficient below 250kcal/m 2 h°C; stretching the cooled wire to a diameter between 2 and 7 mm; in a gas heating furnace or electric Heating the stretched welding wire to a temperature between 600 and 800°C in a heating furnace; cooling the heated welding wire to below 500°C with a heat transfer coefficient below 250kcal/m 2 h°C; and drawing the cooled welding wire Extend to a diameter between 0.8 and 4 mm.
上述根据本发明的诸工艺可以通过在焊剂脱氢和表皮软化处理之后对直径8至15的焊丝简单地拉伸来制造直径0.8至4mm的药芯焊丝。通过以不产生火花的连续流水工序来直接电加热直径8至15mm的直无缝药芯焊丝以及用250kcal/m2h℃以下的传热系数把所加热的焊丝冷却到500℃以下,可以得到每100g熔敷金属含扩散氢不超过5ml的无缝药芯焊丝。然后直径8至12mm的脱氢处理后的焊丝被拉伸成直径2至4mm的其表皮的硬度被控制于180至250Hv的维氏硬度的无缝药芯焊丝。当未加工焊丝直径限于大约8至12mm之间时,可以得到直径0.8至1.6mm,表皮硬度控制于200至250Hv维氏硬度的无缝药芯焊丝。此外,将要热处理的未加工焊丝的直径和已加工焊丝的硬度可以根据用来制造毛坯管的钢带的化学成分从很宽的范围中选择。The above-mentioned processes according to the present invention can produce flux-cored wires with a diameter of 0.8 to 4 mm by simply drawing a wire with a diameter of 8 to 15 mm after flux dehydrogenation and skin softening treatment. By directly heating the straight seamless flux-cored welding wire with a diameter of 8 to 15 mm in a continuous flow process without sparks and cooling the heated welding wire to below 500 °C with a heat transfer coefficient below 250 kcal/m 2 h °C, it can be obtained Seamless flux-cored welding wire containing no more than 5ml of diffusible hydrogen per 100g of deposited metal. Then the dehydrogenated welding wire with a diameter of 8 to 12 mm is drawn into a seamless flux cored wire with a diameter of 2 to 4 mm whose skin hardness is controlled to a Vickers hardness of 180 to 250 Hv. When the diameter of the raw wire is limited to about 8 to 12 mm, a seamless flux cored wire with a diameter of 0.8 to 1.6 mm and a skin hardness controlled at 200 to 250 Hv Vickers hardness can be obtained. In addition, the diameter of the green wire to be heat-treated and the hardness of the processed wire can be selected from a wide range depending on the chemical composition of the steel strip used to manufacture the blank tube.
通过对直径在8与15mm之间的未加工焊丝进行脱氢和表皮软化热处理并将焊丝直径拉伸至2与7mm之间,可以制造超低氢焊丝。首先,用直接电加热对直径在8与15mm之间的未加工焊丝进行脱氢处理。然后,在连续煤气或电加热炉中加热被拉伸到直径2至7mm的焊丝以便表皮软化和脱氢处理。这样得到的产品是每100g熔敷金属含扩散氢不超过3ml的、表皮硬度控制于150至250Hv维氏硬度的超低氢药芯焊丝。Ultra-low hydrogen welding wire can be manufactured by dehydrogenating and skin softening heat-treating raw wire with a diameter between 8 and 15 mm and drawing the wire to a diameter between 2 and 7 mm. First, green wire with a diameter between 8 and 15 mm was dehydrogenated with direct electrical heating. The wire, drawn to a diameter of 2 to 7 mm, is then heated in a continuous gas or electric furnace for skin softening and dehydrogenation. The product obtained in this way is an ultra-low hydrogen flux-cored welding wire which contains no more than 3ml of diffusible hydrogen per 100g of deposited metal and whose skin hardness is controlled at 150 to 250Hv Vickers hardness.
根据本发明的诸工艺消除了对预烘烤填充焊剂的需要。即使焊剂含有很多水也不需要预烘烤或其他强干燥处理。通过对直径8至15mm的未加工管进行脱氢处理和对拉伸到2至7mm直径的管进行附加脱氢处理,不用任何这类预烘烤强干燥处理即可得到每100g熔敷金属含扩散氢不超过3ml的超低氢药芯焊丝。Processes according to the present invention eliminate the need for pre-baking filler flux. Even if the flux contains a lot of water, no pre-baking or other strong drying treatment is required. By dehydrogenation of raw tubes with a diameter of 8 to 15 mm and additional dehydrogenation of tubes stretched to a diameter of 2 to 7 mm, without any such pre-baking strong drying treatment, the concentration per 100 g of deposited metal can be obtained. Ultra-low hydrogen flux-cored welding wire with diffusible hydrogen not exceeding 3ml.
本发明的诸工艺还消除了常规上遇到的调整含有结晶水或氢的焊剂材料的麻烦。对直径在8与15mm之间的焊丝以最高1100℃的温度进行脱氢处理与随后对拉伸到直径2至7mm的焊丝的脱氢处理相结合,使得不用调整填充焊药中所含的结晶水或氢即能制造每100g熔敷金属含扩散氢不超过3ml的超低氢药芯焊丝。The processes of the present invention also eliminate the trouble conventionally encountered in conditioning flux materials containing crystallization water or hydrogen. The dehydrogenation of wires with diameters between 8 and 15 mm at temperatures up to 1100 °C combined with the subsequent dehydrogenation of wires drawn to diameters of 2 to 7 mm makes it unnecessary to adjust the crystallization contained in the filler flux Water or hydrogen can produce ultra-low hydrogen flux-cored wire with no more than 3ml of diffusible hydrogen per 100g of deposited metal.
此外,在分离的工序中进行脱氢加热和表皮软化加热可以为每种加热选择最佳条件。在分离工序中进行脱氢和表皮软化最佳加热的措施可以在焊接期间发生软管严重弯曲的条件下仍然保证提高了的脱氢和稳定的送丝。In addition, performing dehydrogenation heating and skin softening heating in separate processes enables selection of optimal conditions for each heating. Optimum heating measures for dehydrogenation and skin softening in the separation process ensure enhanced dehydrogenation and stable wire feeding even under severe bending of the hose during welding.
图1表示根据本发明对穿过环心变压器的焊丝进行直接电加热的原理。Figure 1 shows the principle of direct electrical heating of welding wire passing through a toroidal transformer according to the invention.
图2图解表示在软化退火之后表皮硬度控制区与直径8至15mm的焊丝的表皮硬度之间的关系。Fig. 2 graphically shows the relationship between the skin hardness control zone and the skin hardness of welding wires having a diameter of 8 to 15 mm after softening annealing.
图3图解表示在软化退火之后表皮硬度控制区与经加热并拉伸到直径2至7mm的焊丝的表皮硬度之间的关系。Fig. 3 graphically shows the relationship between the skin hardness control region and the skin hardness of a welding wire heated and drawn to a diameter of 2 to 7 mm after softening annealing.
图4用曲线表示在直接电加热和隧道式拱炉中加热的结合中的加热时间与温度之间的关系。Figure 4 graphically represents the relationship between heating time and temperature in a combination of direct electrical heating and heating in a tunnel furnace.
图5用曲线表示在连续隧道式拱炉中加热时加热时间与温度之间的关系。Fig. 5 graphically shows the relationship between heating time and temperature when heating in a continuous tunnel furnace.
图6用曲线表示扩散氢数量与水平位置和填角焊中氢诱发裂缝发生率之间的关系。Figure 6 graphically shows the relationship between the amount of diffusible hydrogen and the horizontal position and incidence of hydrogen-induced cracking in fillet welds.
图7用曲线表示扩散氢数量、所形成的缩孔数及气隙发生率之间的关系。Fig. 7 graphically shows the relationship between the amount of diffusible hydrogen, the number of shrinkage cavities formed, and the occurrence rate of air gaps.
图8用曲线表示示例1中加热时间、药芯焊丝的表皮温度及焊剂温度之间的关系。FIG. 8 graphically shows the relationship among the heating time, the skin temperature of the flux-cored wire, and the flux temperature in Example 1. FIG.
图9用曲线表示示例2中加热时间、药芯焊丝的表皮温度及焊剂温度之间的关系。FIG. 9 graphically shows the relationship among the heating time, the skin temperature of the flux-cored wire, and the flux temperature in Example 2. FIG.
图10用曲线表示示例3中加热时间、药芯焊丝的表皮温度及焊剂温度之间的关系。FIG. 10 graphically shows the relationship among the heating time, the skin temperature of the flux-cored wire, and the flux temperature in Example 3. FIG.
图11是表示示例3中加热时间、药芯焊丝的表皮温度及焊剂温度之间关系的另一个曲线图。11 is another graph showing the relationship among the heating time, the skin temperature of the flux-cored wire, and the flux temperature in Example 3. FIG.
图12用曲线表示每个示例中加热时间与扩散氢数量之间的关系。Fig. 12 graphically shows the relationship between the heating time and the amount of diffusible hydrogen in each example.
以下段落参照诸附图描述本发明的细节。The following paragraphs describe the details of the invention with reference to the drawings.
图1表示根据本发明对穿过环心变压器的焊丝进行直接电加热的原理。如图1中的示,一对辊电极装置2和3布置成其间留有给定的距离,而一条焊丝1被夹在组成辊装置2和3的对置辊电极2a与2b及3a与3b之间。动焊丝1在保持与成对辊电极2a与2b及3a与3b的圆周表面相接触的同时向前走行。Figure 1 shows the principle of direct electrical heating of welding wire passing through a toroidal transformer according to the invention. As shown in FIG. 1, a pair of
一个环心变压器4居中布置在成对辊电极装置2和3之间,致使该焊丝穿过变压器上的开口。此变压器包括例如一个铁心,该铁心由一些具有形成磁路的理想性质的中空方形电工钢片组成,它们叠合到想要的厚度,在中心形成一个方形漏空开口。该变压器4有一个绕在与相邻一边相隔90°布置的四个边中的每一个上的长导线初级线圈5。该初级线圈5的两端连接于电源E。辊电极2和3之间借助于导电构件6彼此电气连接。导电构件6的连接端通过滑块7与辊电极可滑动地保持接触。A
既然导电构件6的横截面积和材料可以按希望选择,所以很容易把所加热焊丝的电阻R1对导电构件的电阻R2之比保持为R1>>R2。通过该电路的电流迅速而高效地把焊丝加热到高达1100℃的温度。在火花发生率很低时,功率效率高达90至95%,而相比之下高频感应加热中约50%。由于次级阻抗可以保持低于初级阻抗,所以电压波动很小。由于电源电压消耗于加热第一与第二辊电极之间的焊丝,所以第一和第二辊电极装置具有大体上相等的电位。由于第一和第二辊电极装置因而可以接地,所以电流不会从第一与第二辊电极装置之间外漏。此外,辊电极装置布置成间隔不超过2至5m有助于使加热装置结构紧凑。Since the cross-sectional area and material of the
通过环心变压器可以进行迅速的直接电加热以便同时或分别达成最佳脱氢和表皮软化。在分开的工序中,脱氢加热到620与1100℃之间在前阶段中进行以便减少扩散氢的数量。表皮软化加热到600与800℃之间在后阶段中进行,以此控制表皮的硬度(提高送丝速度并防止焊丝断裂)。如果前阶段中的脱氢对运动较慢的较大直径焊丝进行,则随后的拉伸和表面处理将足以得到想要的产品。因此,最好是对直径8与15之间的较大直径焊丝进行脱氢处理。Rapid direct electrical heating via toroidal transformers for optimal dehydrogenation and skin softening simultaneously or separately. In a separate process, dehydrogenation heating to between 620 and 1100° C. is performed in a preceding stage in order to reduce the amount of diffusible hydrogen. Skin softening Heating to between 600 and 800°C is performed in a later stage to control the hardness of the skin (increase wire feed speed and prevent wire breakage). If the dehydrogenation in the preceding stage is performed on a slower moving larger diameter wire, the subsequent drawing and surface treatment will be sufficient to obtain the desired product. Therefore, it is best to dehydrogenate larger diameter wires between 8 and 15mm in diameter.
如果在前阶段中对运动得慢于较细者的8与15mm之间的较大直径焊丝进行脱氢处理,则除了随后的拉伸之外不需要任何其他工序即可得到含扩散氢不超过5ml的焊丝。用含水量多于非粘合焊剂的粘合焊剂来制造超低氢焊丝是无效的,因为多余的水分必须通过进行预烘烤或其他强干燥处理来去除。相反,对直径在8与15mm之间的较大直径焊丝的脱氢处理与随后对直径2至7mm的已减径焊丝的加热,该加热主要旨在软化表皮但同时也会实现某些附加的脱氢处理的结合,可以用仅稍为干燥的粘合焊剂制造含扩散氢不超过3ml的超低氢焊丝。If larger diameter wires between 8 and 15 mm moving slower than the thinner ones are dehydrogenated in a previous stage, no further process than subsequent drawing is required to obtain 5ml of welding wire. It is ineffective to make ultra-low hydrogen wires with bonded fluxes that contain more water than non-bonded fluxes because the excess water must be removed by prebaking or other intensive drying treatments. Conversely, dehydrogenation of larger diameter wires between 8 and 15 mm in diameter with subsequent heating of reduced diameter wires from 2 to 7 mm in diameter mainly aimed at softening the skin but also achieving some additional The combination of dehydrogenation treatment makes it possible to manufacture ultra-low hydrogen welding wire containing no more than 3ml of diffusible hydrogen with only slightly dry bonding flux.
图2表示直径8至15mm的焊丝表皮硬度与软化退火后表皮硬度控制区之间的关系,而图3表示拉伸到直径2至7mm的焊丝在加热之后的表皮硬度与软化加热之后的表皮硬度控制区之间的关系。如图2和图3中所示,直径8至15mm的焊丝与直径2至7mm的焊丝之间稳定送丝区不同。送丝机构和焊接点相隔几米或几十米并由软管连接。当该软管不得不弯曲以满足工作现场的条件时,如在限定的空间内焊接弯线时,在软管内壁与经过的焊丝之间产生的很大阻力将削弱送丝的稳定性。Figure 2 shows the relationship between the skin hardness of welding wires with a diameter of 8 to 15 mm and the skin hardness control zone after softening annealing, while Figure 3 shows the skin hardness after heating and the skin hardness after softening heating of welding wires drawn to a diameter of 2 to 7 mm Relationships between control areas. As shown in Fig. 2 and Fig. 3, the stable wire feeding zone is different between the welding wire with a diameter of 8 to 15 mm and the welding wire with a diameter of 2 to 7 mm. The wire feeding mechanism and the welding point are separated by a few meters or tens of meters and connected by a hose. When the hose has to be bent to meet job site conditions, such as when welding bends in a confined space, the high resistance created between the inner wall of the hose and the passing welding wire will impair the stability of the wire feeding.
由于阻力值随软管的弯曲状况和焊丝直径而变化,所以必须制备具有适当的表皮硬度以满足作业现场条件的焊丝。随着填充比加大,表皮硬度降低,如图3中所示。表皮硬度超过250Hv的焊丝易于断裂并使其端头难以绕过卷轴。这是弯断极限。另一方面,表皮硬度低于150Hv的焊丝易于在送丝辊与软管之间或在电源尖端的入口端部翘曲并损害送丝的平滑性。这是翘曲极限。因此,当表皮硬度保持在250Hv的弯断极限与150Hv的翘曲极限之间时即可得到稳定送丝区。Since the resistance value varies with the bending condition of the hose and the wire diameter, it is necessary to prepare a welding wire with an appropriate skin hardness to meet the job site conditions. As the filling ratio increases, the skin hardness decreases, as shown in Figure 3. Welding wire with a skin hardness exceeding 250 Hv tends to break and make it difficult to pass the tip around the spool. This is the breaking limit. On the other hand, welding wire with a skin hardness of less than 150 Hv tends to warp between the wire feed roller and the hose or at the inlet end of the power tip and impair the smoothness of wire feeding. This is the warp limit. Therefore, a stable wire feeding zone can be obtained when the hardness of the skin is kept between the breaking limit of 250Hv and the warping limit of 150Hv.
图4表示在直接电加热与隧道式拱炉中加热相结合的工序中加热时间与温度之间的关系。可以看到,直接电加热把表皮温度迅速提高到800℃。然后,与表皮内表面相接触的那部分焊剂的温度上升到400℃并沿着焊剂温度曲线A继续上升。随着热量传过焊剂,焊剂中心部分的温度沿着带有某些时间滞后的焊剂温度曲线B上升,在大约5分钟内达到与表皮温度基本上相同的值。图5表示在利用连续隧道式拱炉的加热工序中加热时间与温度之间的关系。与图4中所示的情形不同,表皮温度在2至3分钟内逐渐上升到800℃。焊剂温度也在大约8分钟之内慢慢上升到800℃。从以上可见,直接电加热可以迅速加热到高温,可以通过直接连接若干工序进行连续的流水加热,并可以以高热效率加热较大直径或较薄表皮的焊丝。Figure 4 shows the relationship between heating time and temperature in a process in which direct electric heating is combined with heating in a tunnel-type arc furnace. It can be seen that direct electric heating rapidly increases the skin temperature to 800°C. Then, the temperature of the part of the flux that is in contact with the inner surface of the skin rises to 400°C and continues to rise along the flux temperature curve A. As heat is transferred through the flux, the temperature of the core portion of the flux rises along the flux temperature curve B with some time lag, reaching substantially the same value as the skin temperature in about 5 minutes. Fig. 5 shows the relationship between heating time and temperature in a heating process using a continuous tunnel furnace. Unlike the situation shown in Fig. 4, the skin temperature gradually increased to 800°C within 2 to 3 minutes. The flux temperature was also ramped up to 800°C in about 8 minutes. It can be seen from the above that direct electric heating can quickly heat to high temperature, and can carry out continuous flowing water heating by directly connecting several processes, and can heat welding wire with larger diameter or thinner skin with high thermal efficiency.
图6表示扩散氢数量与在水平和填角焊接中的氢诱发裂缝之间的关系。换句话说,此图表示100g熔敷金属中所含扩散氢的数量与焊接金属的抗拉强度之间的关系。当扩散氢的含量为5ml时,焊接金属的抗拉强度锐减到60kgf/mm2(=60×9.8×106Pa)。当该含量超过7ml时,该抗拉强度降到50kgf/mm2(=50×9.8×106Pa)且氢诱发断裂的可能性增加。因此,最好把100g熔敷金属中扩散氢含量保持在5ml以下。Figure 6 shows the relationship between the amount of diffusible hydrogen and hydrogen-induced cracking in horizontal and fillet welds. In other words, this graph shows the relationship between the amount of diffusible hydrogen contained in 100 g of deposited metal and the tensile strength of weld metal. When the content of diffusible hydrogen is 5ml, the tensile strength of the weld metal drops sharply to 60kgf/mm 2 (=60×9.8×10 6 Pa). When the content exceeds 7 ml, the tensile strength drops to 50 kgf/mm 2 (=50×9.8×10 6 Pa) and the possibility of hydrogen-induced fracture increases. Therefore, it is best to keep the diffusible hydrogen content in 100g of deposited metal below 5ml.
图7表示扩散氢数量、所形成的缩孔数以及气隙发生率(即底层涂料防护质量)之间的关系。在图7中,熔敷金属是通过对由20μm厚的无机锌底层涂料所覆盖的钢板进行水平填角焊而得到的金属,扩散氢数量是100g熔敷金属中的含量,而缩孔数和气隙发生率是50cm长的焊缝中的值。如图7中所示,缩孔数和气隙发生率在扩散氢含量超过10ml时有锐增的趋势。为了保持良好的底层涂料防护质量,必须把扩散氢含量保持为低于10ml。考虑到图6中所示的抗氢诱发裂缝力和图7中所示的底层涂料防护质量,必须把扩散氢含量保持为起码低于7ml,最好低于5ml。根据本发明无缝药芯焊丝的最佳焊剂填充比为10至26%。Figure 7 shows the relationship between the amount of diffusible hydrogen, the number of shrinkage cavities formed, and the incidence of air voids (ie, the protective quality of the primer). In Fig. 7, the deposited metal is the metal obtained by horizontal fillet welding of a steel plate covered with a 20 μm thick inorganic zinc primer, the amount of diffusible hydrogen is the content in 100 g of the deposited metal, and the number of shrinkage cavities and gas The gap occurrence rate is a value in a 50 cm long weld. As shown in Fig. 7, the number of shrinkage cavities and the occurrence rate of air voids tend to sharply increase when the diffusible hydrogen content exceeds 10ml. In order to maintain good primer protection qualities, it is necessary to keep the diffusible hydrogen content below 10ml. Considering the resistance to hydrogen-induced cracking shown in Figure 6 and the protective quality of the primer shown in Figure 7, it is necessary to keep the diffusible hydrogen content at least below 7ml, preferably below 5ml. The optimal flux filling ratio of the seamless flux cored wire according to the present invention is 10 to 26%.
示例example
示例1Example 1
一种用于JIS Z#3313 YEW-C50DR标准无缝药芯焊丝、内腔填充焊剂至15%(按重量)的21mm直径未加工焊丝,承受拉伸以减轻到10mm,使该内腔被焊剂填充到100%以上(按体密度)为了进行脱氢处理,通过使该焊丝以20m/min(≈0.333m/s)的速度穿过布置在相距5m的第一与第二辊电极装置之间的环心变压器,以72℃/S的速度把该10mm直径的焊丝直接电加热到1080℃。图8表示表皮温度与焊剂温度之间的关系。更具体地说,图8表示加热时间与药芯焊丝表皮温度及焊剂温度之间的关系。在电加热后,表皮温度立即迅速上升到1080℃而与表皮内表面相接触的那部分焊剂的温度迅速上升到300℃并沿着焊剂温度曲线A继续上升。随着热量传过焊剂,焊剂中心部分的温度沿着带有某些时间滞后的焊剂温度曲线B上升,在1分钟之内达到大约950℃,如图8中所示。所加热的焊丝以50kcal/m2h(≈42.996W/(m2·K),下同)℃的传热系数被空冷4分钟,然后在500℃以下以2.4℃/S的快速受控冷却速率水冷。然后该焊丝承受拉伸和表面处理工序以得到直径2.4mm的成品焊丝。这样得到的该2.4mm直径焊丝用于在42V、35cm/min(≈0.058m/s,下同)的焊接速度、30mm的焊丝延伸及30L/min(≈0.5×10-3m3/s,下同)的二氧化碳放气量下用550V的焊接。用气相色变法测定的所得到的每100g熔敷金属的扩散氢含量为4.2ml。A 21mm diameter unprocessed welding wire for JIS Z#3313 YEW-C50DR standard seamless flux-cored welding wire, the inner cavity is filled with flux to 15% (by weight), subjected to tension to reduce to 10mm, so that the inner cavity is filled with flux Filled to more than 100% (according to bulk density) in order to carry out dehydrogenation treatment, by making the welding wire pass through the first and second roller electrode devices arranged at a distance of 5m at a speed of 20m/min (≈0.333m/s) The toroidal transformer is used to directly heat the welding wire with a diameter of 10mm to 1080°C at a speed of 72°C/S. Fig. 8 shows the relationship between skin temperature and flux temperature. More specifically, FIG. 8 shows the relationship between the heating time and the cored wire skin temperature and flux temperature. After electric heating, the temperature of the skin rises rapidly to 1080°C immediately, and the temperature of the part of the flux that is in contact with the inner surface of the skin rises rapidly to 300°C and continues to rise along the flux temperature curve A. As heat is transferred through the flux, the temperature of the core portion of the flux rises along the flux temperature curve B with some time lag, reaching about 950° C. within 1 minute, as shown in FIG. 8 . The heated welding wire is air-cooled for 4 minutes with a heat transfer coefficient of 50kcal/m 2 h (≈42.996W/(m 2 ·K), the same below)°C, and then cooled rapidly and controlled at 2.4°C/S below 500°C Rate water cooling. The wire was then subjected to drawing and surface treatment processes to obtain a finished wire with a diameter of 2.4 mm. The 2.4mm diameter welding wire thus obtained is used at 42V, a welding speed of 35cm/min (≈0.058m/s, the same below), a welding wire extension of 30mm, and 30L/min (≈0.5×10 -3 m 3 /s, The same below) use 550V welding under the amount of carbon dioxide outgassing. The obtained diffusible hydrogen content per 100 g of the deposited metal measured by the gas chromatography method was 4.2 ml.
示例2Example 2
一种用于JIS Z3313 YEW-C50DR标准无缝药芯焊丝内腔填充焊剂至18%(按重量)21.5mm直径的未加工焊丝,承受拉伸和表面处理工序以减轻到10.5mm,使该内腔被焊剂填充到100%以上(按体密度)。为了进行脱氢处理,通过使该焊丝以20m/min的速度穿过布置在相距5m的第一与第二辊电极装置之间的环心变压器,以53℃/S的速率把该10.5mm直径的焊丝直接电加热到800℃。图9表示表皮温度与焊剂温度之间的关系。更具体地说,图9表示加热时间与药芯焊丝表皮温度及焊剂温度之间的关系。在电加热后,表皮温度立即迅速上升到800℃而与表皮内表面相接触的那部分焊剂的温度迅速上升到200℃并沿着焊剂温度曲线A继续上升。随着热量传过焊剂,焊剂中心部分的温度沿着带有某些时间滞后的焊剂温度曲线B上升,在1分钟之内达到大约800℃,如图9中所示。所加热的焊丝在直接连接的煤气或连续加热炉中在800℃下再加热2分钟,以50kcal/m2h℃的传热系数空冷2分钟,然后在500℃以下通过以2.5℃/S的速率的迅速受控冷却来水冷。然后该焊丝承受拉伸和表面处理工序以得到直径2.0mm的成品焊丝。这样得到的该2.0mm直径焊丝用于在38V、35cm/min的焊接速度、25mm的焊丝延伸及25L/min(=4.167×10-4m3/s,下同)的二氧化碳放气量下用500A的焊接。用气相色谱法测定的所得到的每100g熔敷金属的扩散氢含量为4.5ml。A raw welding wire for JIS Z3313 YEW-C50DR standard seamless flux-cored wire lumen filled with flux to 18% (by weight) 21.5mm in diameter, subjected to stretching and surface treatment processes to lighten to 10.5mm, so that the inner The cavity is filled to more than 100% (by bulk density) with flux. For the dehydrogenation treatment, the 10.5 mm diameter wire is passed at a rate of 53 ° C / S by passing the welding wire at a speed of 20 m / min through the toroidal transformer arranged between the first and second roll electrode devices at a distance of 5 m. The welding wire is directly heated to 800°C. Fig. 9 shows the relationship between skin temperature and flux temperature. More specifically, FIG. 9 shows the relationship between the heating time and the cored wire skin temperature and flux temperature. After electric heating, the temperature of the skin immediately rises rapidly to 800°C, and the temperature of the part of the flux that is in contact with the inner surface of the skin rises rapidly to 200°C and continues to rise along the flux temperature curve A. As heat is transferred through the flux, the temperature of the central portion of the flux rises along the flux temperature curve B with some time lag, reaching about 800° C. within 1 minute, as shown in FIG. 9 . The heated welding wire is reheated at 800°C for 2 minutes in a directly connected gas or continuous heating furnace, cooled in air with a heat transfer coefficient of 50kcal/m 2 h°C for 2 minutes, and then passed through a temperature of 2.5°C/S below 500°C Rapid and controlled cooling of the rate comes with water cooling. The wire was then subjected to drawing and surface treatment processes to obtain a finished wire with a diameter of 2.0 mm. The 2.0mm diameter welding wire obtained in this way is used to use 500A welding wire at 38V, 35cm/min welding speed, 25mm welding wire extension and 25L/min (=4.167×10 -4 m 3 /s, the same below) carbon dioxide outgassing. of welding. The resultant diffusible hydrogen content measured by gas chromatography was 4.5 ml per 100 g of the deposited metal.
示例3Example 3
一种用于JIS Z#3313 YEW-C50DR标准无缝药芯焊丝V、内腔填充焊剂至12%(按重量)的21mm直径未加工焊丝,承受拉伸以减轻到10mm,使该内腔被焊剂填充到100%以上(按体密度)。为了进行脱氢处理,通过使该焊丝以60m/min(=1m/s,下同)的速度穿过布置在相距2.5m的第一与第二辊电极装置之间的环心变压器,以350℃/S的速率把该10mm直径的焊丝直接电加热到880℃。图10表示表皮温度与焊剂温度之间的关系。更具体地说,图10表示加热时间与药芯焊丝表皮温度及焊剂温度之间的关系。在电加热后,表皮温度立即迅速上升到880℃而与表皮内表面相接触的那部分焊剂的温度迅速上升到200℃并沿着焊剂温度曲线A继续上升。随着热量传过焊剂,焊剂中心部分的温度沿着带有某些时间滞后的焊剂温度曲线B上升,在1分钟之内达到大约800℃,如图10中所示。所加热的焊丝以20kcal/m2h℃(≈17.16W/(m2·K),下同)的传热系数被空冷4分钟,然后在500℃以下以1.6℃/S的速率的迅速受控冷却水冷。然后该焊丝被拉伸成直径3.2mm的焊丝,此焊丝在隧道式拱炉中加热到800℃5分钟,以便表皮软化和脱氢。图11表示所得到的表皮温度与焊剂温度之间的关系。更具体地说,图11表示加热时间与药芯焊丝表皮温度和焊剂温度之间的关系。如图11中所示,表皮温度在3分钟内上升到800℃。焊剂温度在6分钟内也上升到大约800℃。所加热焊丝以80kcal/m2h℃(≈68.64W/(m2·K),下同)的传热系数再次被空冷3分钟,然后在400℃以下以2.2℃/S的速率的迅速受控冷却水冷。然后该焊丝承受拉伸和表面处理以得到直径1.2mm的成品焊丝。这样得到的该1.2mm直径焊丝用于在30V、35cm/min的焊接速度、20mm的焊丝延伸及25L/min的二氧化碳放气量下用270A的焊接。用气相色谱法测定的所得到的每100g熔敷金属的扩散氢含量为2.1ml。A 21 mm diameter unprocessed welding wire for JIS Z#3313 YEW-C50DR standard seamless flux cored wire V, filled with flux to 12% (by weight) in the inner cavity, subjected to tension to reduce to 10mm, so that the inner cavity is Flux filled to more than 100% (by bulk density). In order to carry out the dehydrogenation treatment, by making the welding wire pass through the toroidal transformer arranged between the first and second roll electrode devices at a distance of 2.5 m at a speed of 60 m/min (=1 m/s, the same below), the wire is heated at 350 The 10mm diameter welding wire was directly electrically heated to 880°C at a rate of °C/S. Fig. 10 shows the relationship between skin temperature and flux temperature. More specifically, FIG. 10 shows the relationship between the heating time and the cored wire skin temperature and flux temperature. After electric heating, the temperature of the skin rises rapidly to 880°C immediately and the temperature of the part of the flux that is in contact with the inner surface of the skin rises rapidly to 200°C and continues to rise along the flux temperature curve A. As heat is transferred through the flux, the temperature of the central portion of the flux rises along the flux temperature curve B with some time lag, reaching about 800°C within 1 minute, as shown in FIG. 10 . The heated welding wire is air-cooled for 4 minutes with a heat transfer coefficient of 20kcal/m 2 h°C (≈17.16W/(m 2 ·K), the same below), and then rapidly heated at a rate of 1.6°C/S below 500°C. Control cooling water cooling. The wire was then drawn to a diameter of 3.2 mm, which was heated to 800° C. for 5 minutes in a tunnel furnace to soften the skin and dehydrogenate it. Fig. 11 shows the obtained relationship between the skin temperature and the flux temperature. More specifically, Fig. 11 shows the relationship between the heating time and the cored wire skin temperature and flux temperature. As shown in Figure 11, the skin temperature rose to 800°C within 3 minutes. The flux temperature also rose to about 800°C within 6 minutes. The heated welding wire is air-cooled again for 3 minutes with a heat transfer coefficient of 80kcal/m 2 h°C (≈68.64W/(m 2 ·K), the same below), and then rapidly heated at a rate of 2.2°C/S below 400°C. Control cooling water cooling. The wire was then subjected to drawing and surface treatment to obtain a finished wire with a diameter of 1.2 mm. The 1.2mm diameter welding wire thus obtained was used for welding at 270A at 30V, welding speed of 35cm/min, wire extension of 20mm and carbon dioxide outgassing of 25L/min. The obtained diffusible hydrogen content per 100 g of the deposited metal measured by gas chromatography was 2.1 ml.
图12表示每个示例中加热时间与扩散氢数量之间的关系。100g熔敷金属中扩散氢的数量在示例1中为4.2ml,在示例2中为4.5ml,在示例3中在直接电加热到880℃,并在空冷后在500℃下水冷的焊丝中为5.0ml,而在继续在隧道式拱炉中加热并被冷却的焊丝中为2.1ml。显然,用本发明的工艺制备的所有焊丝含有比常规焊丝低得多的扩散氢,该常规焊丝是为了对比未经加热而制备的。于是根据本发明的诸工艺通过降低扩散氢的含量可以高效地制造低氢药芯焊丝,该焊丝具有优异的抗裂缝力和底层涂料防护质量,适合于高强度钢和结构钢的焊接。Fig. 12 shows the relationship between the heating time and the amount of diffusible hydrogen in each example. The amount of diffusible hydrogen in 100g of deposited metal is 4.2ml in Example 1, 4.5ml in Example 2, and in Example 3 in the welding wire which is directly electrically heated to 880°C and water-cooled at 500°C after air cooling is 5.0ml, and 2.1ml in the welding wire that continues to be heated and cooled in the tunnel arc furnace. It is evident that all welding wires prepared by the process of the present invention contained much lower diffusible hydrogen than the conventional welding wire prepared for comparison without heating. Therefore, the processes according to the present invention can efficiently produce low-hydrogen flux-cored welding wire by reducing the content of diffusible hydrogen, which has excellent crack resistance and primer protection quality, and is suitable for welding high-strength steel and structural steel.
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN97102700A CN1102480C (en) | 1997-02-27 | 1997-02-27 | Process for manufacturing welding wire |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN97102700A CN1102480C (en) | 1997-02-27 | 1997-02-27 | Process for manufacturing welding wire |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1191790A CN1191790A (en) | 1998-09-02 |
CN1102480C true CN1102480C (en) | 2003-03-05 |
Family
ID=5166375
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN97102700A Expired - Fee Related CN1102480C (en) | 1997-02-27 | 1997-02-27 | Process for manufacturing welding wire |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1102480C (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111315521A (en) * | 2017-06-09 | 2020-06-19 | 伊利诺斯工具制品有限公司 | Method and system for heating welding wire to reduce hydrogen content |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102909495A (en) * | 2012-10-08 | 2013-02-06 | 韩永艾 | Method for producing CO2 gas shield solid welding wire by physical oxidation method |
CN104263898A (en) * | 2014-09-24 | 2015-01-07 | 河南科技大学 | Drawing and annealing method for flux cored wire production process |
CN104263897A (en) * | 2014-09-24 | 2015-01-07 | 河南科技大学 | Drawing and annealing system for flux cored wire production process |
EP3242756B1 (en) | 2015-01-09 | 2021-04-14 | Illinois Tool Works Inc. | Inline resistive heating system and method for thermal treatment of continuous conductive products |
US10675699B2 (en) | 2015-12-10 | 2020-06-09 | Illinois Tool Works Inc. | Systems, methods, and apparatus to preheat welding wire |
US11344964B2 (en) | 2017-06-09 | 2022-05-31 | Illinois Tool Works Inc. | Systems, methods, and apparatus to control welding electrode preheating |
US11524354B2 (en) | 2017-06-09 | 2022-12-13 | Illinois Tool Works Inc. | Systems, methods, and apparatus to control weld current in a preheating system |
CA3066650C (en) * | 2017-06-09 | 2022-09-13 | Illinois Tool Works Inc. | Coaxial laser hotwire head |
WO2020132251A2 (en) | 2018-12-19 | 2020-06-25 | Illinois Tool Works Inc. | Systems, methods and apparatus to preheat welding wire |
CN110863085B (en) * | 2019-11-14 | 2022-01-04 | 中国京冶工程技术有限公司 | Stress on-line control method suitable for flux-cored wire for steel structure |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58110195A (en) * | 1981-12-22 | 1983-06-30 | Kobe Steel Ltd | Production of flux cored wire electrode for stainless steel |
JPS5961597A (en) * | 1982-09-30 | 1984-04-07 | Nippon Steel Weld Prod & Eng Co Ltd | Manufacturing method of flux-cored wire for welding |
JPS59130698A (en) * | 1983-01-14 | 1984-07-27 | Nippon Steel Corp | Manufacturing method of stainless steel flux-cored wire |
JPH0481297A (en) * | 1990-07-24 | 1992-03-13 | Kawasaki Steel Corp | Production of flux cored wire for welding |
EP0489167A1 (en) * | 1990-06-21 | 1992-06-10 | NIPPON STEEL WELDING PRODUCTS & ENGINEERING CO., Ltd. | Method of manufacturing tube filled with powder and granular material |
-
1997
- 1997-02-27 CN CN97102700A patent/CN1102480C/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58110195A (en) * | 1981-12-22 | 1983-06-30 | Kobe Steel Ltd | Production of flux cored wire electrode for stainless steel |
JPS5961597A (en) * | 1982-09-30 | 1984-04-07 | Nippon Steel Weld Prod & Eng Co Ltd | Manufacturing method of flux-cored wire for welding |
JPS59130698A (en) * | 1983-01-14 | 1984-07-27 | Nippon Steel Corp | Manufacturing method of stainless steel flux-cored wire |
EP0489167A1 (en) * | 1990-06-21 | 1992-06-10 | NIPPON STEEL WELDING PRODUCTS & ENGINEERING CO., Ltd. | Method of manufacturing tube filled with powder and granular material |
JPH0481297A (en) * | 1990-07-24 | 1992-03-13 | Kawasaki Steel Corp | Production of flux cored wire for welding |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111315521A (en) * | 2017-06-09 | 2020-06-19 | 伊利诺斯工具制品有限公司 | Method and system for heating welding wire to reduce hydrogen content |
Also Published As
Publication number | Publication date |
---|---|
CN1191790A (en) | 1998-09-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1102480C (en) | Process for manufacturing welding wire | |
EP0930131B1 (en) | Method of manufacturing porous electrode wire for electric discharge machining and structure of the electrode wire | |
KR101541790B1 (en) | Process and apparatus for producing solder-plated wire | |
US4020312A (en) | Method of manufacturing thick, high-strength steel pipe for low temperature service | |
CN105051238B (en) | The fused zinc system plated steel sheet and its manufacture method of plating excellent adhesion | |
EP3144399B1 (en) | Method for producing grain-oriented electrical steel sheet | |
RU2674372C1 (en) | Steel pipe, cladded by stainless steel and produced by contact welding, and its production method | |
TWI277656B (en) | High carbon steel wire material having excellent wire drawability and manufacturing process thereof | |
US5821500A (en) | Process for manufacturing welding wire | |
JP6348059B2 (en) | First electrode welding torch for multi-electrode submerged arc welding and welding method using the same | |
EP3202926A1 (en) | Hearth roll and continuous annealing facility | |
JP2000517248A (en) | High tension erosion electrode | |
JP2005232549A (en) | High-strength pc steel wire superior in twisting characteristics | |
JP2010131637A (en) | Gas shielded arc welding method | |
JPH06155076A (en) | Welding method for making thick and large-diameter welded steel pipe | |
JPH023679B2 (en) | ||
JPH1157848A (en) | Copper coated aluminum wire manufacture | |
TW318157B (en) | ||
JP3775051B2 (en) | Flash butt welding apparatus and welding method | |
JP3182984B2 (en) | Manufacturing method of high strength extra fine steel wire | |
JPH0514771B2 (en) | ||
JP2006307335A (en) | Reflow treatment method for metal plating material, metal plating material, and reflow treatment device for metal plating material | |
JP2000233295A (en) | Solid wire for gas shield arc welding | |
JPS61262484A (en) | Production of stainless clad steel pipe having excellent corrosion resistance and toughness | |
JPS597803B2 (en) | Manufacturing method of high strength and high modulus graphite fiber |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
REG | Reference to a national code |
Ref country code: HK Ref legal event code: GR Ref document number: 1044455 Country of ref document: HK |
|
C19 | Lapse of patent right due to non-payment of the annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |