JP5560504B2 - Tungsten inert gas arc welding flux for steel - Google Patents
Tungsten inert gas arc welding flux for steel Download PDFInfo
- Publication number
- JP5560504B2 JP5560504B2 JP2008232932A JP2008232932A JP5560504B2 JP 5560504 B2 JP5560504 B2 JP 5560504B2 JP 2008232932 A JP2008232932 A JP 2008232932A JP 2008232932 A JP2008232932 A JP 2008232932A JP 5560504 B2 JP5560504 B2 JP 5560504B2
- Authority
- JP
- Japan
- Prior art keywords
- flux
- iron
- welding
- sio
- steel
- 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.)
- Active
Links
Landscapes
- Nonmetallic Welding Materials (AREA)
Description
本発明は溶接の方法についてのものであり、鋼や合金のイナートガスアーク溶接(TIG溶接)用の活性フラックスに関するものである。本発明は工業製品に不可欠な、1パスあるいは複数パスの、手動または自動溶接で使用する。 The present invention relates to a welding method and relates to an active flux for inert gas arc welding (TIG welding) of steel and alloys. The present invention is used in one-pass or multi-pass manual or automatic welding, which is essential for industrial products.
当技術分野では、異なるタイプの鋼や合金の溶接深さを深くするための種々な組成の活性フラックス(以下「フラックス」という)が知られている。例えば、(発明者証 1980年4月30日第730515号, IPC7: B23 35/362、B. # 16)や(発明者証 1987年10月7日第1342649号 A1, IPC7: B23 35/362, B. # 37)、(発明者証 1991年12月7日第1696233号 A1, IPC7: B23 35/362, B. # 45)など。 Active fluxes of various compositions (hereinafter referred to as “flux”) for increasing the welding depth of different types of steels and alloys are known in the art. For example, (Inventor ID April 30, 1980 No. 730515, IPC 7 : B23 35/362, B. # 16) and (Inventor ID October 7, 1987 No. 1342649 A1, IPC 7 : B23 35 / 362, B. # 37), (Inventor's certificate December 7, 1991 No. 1696233 A1, IPC 7 : B23 35/362, B. # 45).
フラックスは、フラックス粉末とエチルアルコールのような有機揮発溶液が含まれる懸濁液状で、溶接前に溶接接合部に塗られる。 The flux is a suspension containing flux powder and an organic volatile solution such as ethyl alcohol, and is applied to the weld joint before welding.
イナートガスアーク溶接用のフラックスの従来技術 (発明者証1985年6月23日第1162565号 A, IPC7: B23 35/362, B. # 23)では、高強度ステンレス溶接時のアークによる溶接深さを深くするというものがあり、この特許請求の範囲におけるフラックスの組成は以下である (単位は重量%)。 In the prior art of inert gas arc welding flux (Inventor's certificate June 23, 1985, No. 1162565 A, IPC 7 : B23 35/362, B. # 23), the welding depth by arc during high-strength stainless steel welding The composition of the flux in this claim is as follows (unit:% by weight).
上記フラックスは、化学的に純粋な各組成要素を機械的に混合して作成する。作成したフラックスは、本質的に以下のような欠点を持つ。 The flux is made by mechanically mixing each chemically pure component. The prepared flux essentially has the following disadvantages.
・各組成要素を完全に混合する必要性
・組成要素の中に毒性のものが含まれる(酸化バナジウムなど)
・最大57.5%の多量の低沸点(Tboil)ハロゲン化物塩 (LiFの沸点Tboil = 1949 K、NaFの沸点Tboil = 1975 K)が含まれ、250Aを超える電流での溶接時のフラックス効果の著しい減少
・ Necessity to thoroughly mix each composition element ・ There are toxic substances in the composition element (e.g. vanadium oxide)
・ Contains a large amount of low boiling point (T boil ) halide salt (LiF boiling point T boil = 1949 K, NaF boiling point T boil = 1975 K) up to 57.5%, flux effect during welding at a current exceeding 250A Marked decrease in
以上のような欠点を補うために、他の従来技術では、ステンレスのTIG溶接用のフラックスに以下の組成(重量%)が提案されている(2000年11月28日公開の特開2000−326091、IPC7 B23K 35/362)。
In order to make up for the above-mentioned drawbacks, the following composition (% by weight) has been proposed as a flux for stainless steel TIG welding in other conventional techniques (Japanese Patent Laid-Open No. 2000-326091 published on Nov. 28, 2000). IPC 7 B23K 35/362).
上記組成のフラックスは、溶融池に一定レベル(500-600 dyne/cm)の表面張力を与える。
しかしながら、このフラックスは従来技術のフラックスの欠点の一部である、ハロゲン化物塩が含まれないという点のみについて克服されており、また構成要素が3つであるという特徴を持つ。
The flux having the above composition gives a constant level (500-600 dyne / cm) of surface tension to the molten pool.
However, this flux has been overcome only in that it does not contain halide salts, which is part of the disadvantages of prior art fluxes, and has the characteristic of having three components.
このフラックスには、以下のような本質的な欠点がある。
・溶接深さの減少(特に電流が100A未満の場合)。これは、鋼よりも非常に高い融点(Tmelt)を持つ材料(TiO2のTmelt = 2185 K、SiO2のTmelt = 1996 K、Cr2O3のTmelt = 2548 K)がフラックスに含まれているためである。溶接深さの減少は、アーク電力の一部がベース金属表面の難溶性酸化膜の溶融に使われるためである。
・フラックス懸濁液を使う前の各組成要素の十分な混合の必要性。フラックスの各組成要素の比重(ρ)の大きな違い(2.0〜2.5倍)から(SiO2のρ= 2.3-2.6 g/cm3、Cr2O3のρ = 5.2 g/cm3)、フラックス懸濁液保管中に各要素が分離するため、使用前に十分混合しないと溶接部の幾何学的サイズが不安定になる可能性がある。
・毒性の組成要素が含まれる (Cr2O3).
This flux has the following essential drawbacks.
-Reduced welding depth (especially when the current is less than 100A). This is due to the fact that materials with a very high melting point (T melt ) than steel (TiO 2 T melt = 2185 K, SiO 2 T melt = 1996 K, Cr 2 O 3 T melt = 2548 K) are fluxes. Because it is included. The decrease in welding depth is due to the fact that part of the arc power is used to melt the sparingly soluble oxide film on the base metal surface.
• The need for thorough mixing of each component before using the flux suspension. The main difference between the specific gravity of the composition elements of the flux ([rho) from (2.0 to 2.5-fold) (SiO 2 of ρ = 2.3-2.6 g / cm 3, Cr 2 O 3 of ρ = 5.2 g / cm 3) , suspension flux Each element separates during turbid storage, so the weld geometry may become unstable if not mixed well before use.
Contains toxic components (Cr 2 O 3 ).
本発明の目的は、溶接アークの透過力を確実に高める、環境を汚さないフラックスを提供し、溶接の質を向上させることである。
溶接の質は、懸濁液状のフラックス組成要素が分離し不均一な分布となることに起因する、溶接深さおよび溶接の幅のばらつきを減らすことで向上できる。
It is an object of the present invention to provide a flux that does not pollute the environment, reliably increasing the transmission power of the welding arc, and improving the quality of welding.
The quality of the weld can be improved by reducing variations in weld depth and weld width that result from separation and non-uniform distribution of suspension flux composition elements.
上記本発明の目的は、TIG溶接用フラックスの組成要素が、毒性のものを含まず、フラックスの98%を占める主な組成要素の融点が比較的低融点で、比重値が近い値であることで達成される。本発明によるフラックスはタングステンイナートガスアーク溶接(TIG溶接)用であり、二酸化ケイ素を含んでいる。さらに本フラックスは、メタケイ酸鉄、オルトチタン酸鉄、メタチタン酸鉄、ディチタン酸鉄の混合物であり、これらの各組成比(重量%)が以下であることを特徴とする。 The purpose of the present invention is that the composition element of the flux for TIG welding does not include toxic ones, the melting point of the main composition element that occupies 98% of the flux is a relatively low melting point, and the specific gravity value is close. To be achieved. The flux according to the invention is for tungsten inert gas arc welding (TIG welding) and contains silicon dioxide. Furthermore, this flux is a mixture of iron metasilicate, iron orthotitanate, iron metatitanate, and iron dititanate, and each of these composition ratios (% by weight) is characterized by the following.
・二酸化ケイ素 SiO2 2,0
・メタケイ酸鉄Fe2SiO4
オルトチタン酸鉄Fe2TiO4
メタチタン酸鉄FeTiO3
ディチタン酸鉄FeTi2O5 98,0
・ Silicon dioxide SiO 2 2,0
・ Iron metasilicate Fe 2 SiO 4
Iron orthotitanate Fe 2 TiO 4
Iron metatitanate FeTiO 3
Iron dititanate FeTi 2 O 5 98,0
上記組成は、溶接深さを増加させるため各要素の物理化学的な性質から決められており、そのメカニズムは十分に周知されている。 The above composition is determined from the physicochemical properties of each element in order to increase the welding depth, and the mechanism is well known.
活性フラックス層でのTIG溶接の溶接深さのメカニズムは、金属-フラックス-溶融池-アークシステムの間で起こる以下の主な現象により説明される。 The mechanism of weld depth in TIG welding with an active flux layer is explained by the following main phenomena that occur between the metal-flux-weld pool-arc system:
・アークの陽極領域の収縮
・アーク-フラックス-溶融池の相互作用領域内でのアーク柱の熱出力の再分散
・溶融池金属表面張力の低下
・溶融池金属の溶融方向および溶融速度の変化。溶融池の中心から周辺に向かう外向から、溶融池の周辺から溶融池の中央および内部に向かう、速度の速い内向へ変化する
• Shrinkage of the anode region of the arc • Redispersion of the arc column thermal output within the arc-flux-molten pool interaction region • Reduction of molten pool metal surface tension • Change in melting direction and rate of molten pool metal. Changes from outward facing toward the periphery from the center of the molten pool to inward with high speed from the periphery of the molten pool toward the center and inside of the molten pool
上記溶融深さのメカニズムを基に次のことが言える。従来技術のフラックスにおいて、溶融池の表面張力は溶接の深さに対して重要な影響を与える要因ではあるが、それが唯一あるいは十分な要因ではない。
このような溶融深さのメカニズムから、活性フラックスの各要素には主に以下のような物理化学的な性質が求められる。
The following can be said based on the mechanism of the melting depth. In prior art fluxes, the surface tension of the weld pool is a factor that has a significant effect on the weld depth, but it is not the only or sufficient factor.
From such a melting depth mechanism, each element of the active flux mainly requires the following physicochemical properties.
・解離中の十分な量の酸素発生
・溶融池金属とのアクティブな相互作用
・十分に高い沸点
・低い融点
・フラックスの化学的組成を安定させるような各要素の比重(複数の組成要素を機械的に混合する場合)が近い値であること
・非毒性
-Sufficient oxygen evolution during dissociation-Active interaction with molten pool metal-High enough boiling point-Low melting point-Specific gravity of each element that stabilizes the chemical composition of the flux (multiple compositional elements (When mixed mechanically)
電気陰性度が高く、表面が活性の元素の中では、誘電特性を持つ難溶性化合物を作るのに酸素が最も効率が良いことは周知の事実である。
また、酸素の解離は周知のように以下の式で表わされる。
It is a well-known fact that oxygen is the most efficient in producing poorly soluble compounds with dielectric properties among elements with high electronegativity and active surfaces.
As is well known, oxygen dissociation is represented by the following equation.
ここで、Eは元素、Oは原子状酸素、O2は酸素分子、EOは酸化物、i,jはЕiОj分子の原子数、ηoq,η02,η10,ηmnはm,n-1,2...などの整数の係数である。
例えば、SiO2は3000Kを超える温度で解離し、以下のように気相を形成する。
Here, E is an element, O is atomic oxygen, O 2 is an oxygen molecule, EO is an oxide, i, j is the number of atoms of ЕiOj molecule, η oq , η 02 , η 10 , and η mn are m, n − 1,2. . . Is an integer coefficient.
For example, SiO 2 dissociates at a temperature exceeding 3000K and forms a gas phase as follows.
計算実験から、深い溶接を行うには、沸点における一酸化物の気相中に酸素分子(O2)の存在が必須であることが分かった。気相中の酸素分子含有量の計算値は、酸素の一定比率(4x10-4cm3)中で0.1cm3未満にならないようにしなければならない。また、酸素の沸点は3400K以下であることがわかっている。このような条件に合う酸化物は、
SiO2、TiO2、Cr2O3、MgO、Ga2O3、V2O5、CoO、MnO、FeO、SnO2、GeO2、ZnO、B2O3、およびより高次の酸化物(Fe2O3など)である。
実験結果より、この中で溶接深さに最も効果のある酸化物は、
SiO2、TiO2、Cr2O3、MgO、CoO、MnO、FeOであることがわかった。
From the calculation experiment, it was found that the presence of molecular oxygen (O 2 ) in the vapor phase of monoxide at the boiling point is essential for deep welding. Calculated molecular oxygen content in the gas phase, must to be no less than 0.1 cm 3 in a constant ratio of oxygen (4x10 -4 cm 3). It has also been found that the boiling point of oxygen is 3400K or less. An oxide that meets these conditions
SiO 2, TiO 2, Cr 2 O 3, MgO, Ga 2 O 3, V 2 O 5, CoO, MnO, FeO, SnO 2, GeO 2, ZnO, B 2 O 3, and higher order oxide ( Fe 2 O 3 etc.).
From the experimental results, the most effective oxide for welding depth is
It was found to be SiO 2 , TiO 2 , Cr 2 O 3 , MgO, CoO, MnO, FeO.
SiO2、TiO2、Cr2O3、MnO、Mn2O3、FeO、Fe2O3などの酸化物で構成された溶接スラグ酸化物は、溶融池との最も強い相互作用を示す。
しかしながら、これらの酸化物はすべて融点が高いため、溶接時のアーク-金属-溶融池領域でのアーク電力の再分布により溶接深さが減少する。また、SiO2、TiO2、FeO、Fe2O3は、非毒性の酸化物である。上記酸化物で構成された化学合成物で鋼よりも低い融点を持つものは、Fe2SiO4、FeTiO3、Fe2TiO4である。
Weld slag oxide composed of oxides such as SiO 2 , TiO 2 , Cr 2 O 3 , MnO, Mn 2 O 3 , FeO, and Fe 2 O 3 exhibits the strongest interaction with the molten pool.
However, all of these oxides have a high melting point, and the welding depth is reduced by the redistribution of arc power in the arc-metal-weld pool region during welding. SiO 2 , TiO 2 , FeO, and Fe 2 O 3 are non-toxic oxides. Chemical compounds composed of the above oxides that have a lower melting point than steel are Fe 2 SiO 4 , FeTiO 3 , and Fe 2 TiO 4 .
本発明による活性フラックス中の少量の(2重量%)二酸化ケイ素(SiO2)は、懸濁液で使用する場合、フラックスと有機液体との急速な分離を防ぐためのものである。 A small amount (2% by weight) of silicon dioxide (SiO 2 ) in the active flux according to the invention is intended to prevent rapid separation of the flux from the organic liquid when used in suspension.
活性フラックスの組成要素に、既知の特性のものと新しい機能を持つものを混合させることにより、アーク透過力の高い溶接を提供することができる。 It is possible to provide welding with high arc permeability by mixing active flux compositional elements with known characteristics and new functions.
本発明によるフラックスは、以下の必要条件を満たしている。
・沸点における一酸化物の気相中の酸素分子(O2)の存在が、酸素の一定比率(4x10-4cm3)中で0.1cm3未満
・十分な熱強度(フラックスの沸点は2500〜3266K)
・フラックスの主な組成要素が低融点(鋼の融点(1638〜1673K)より下)
・フラックスの各組成要素の比重が近い値であること(鉄かんらん石:4.3 g/cm3、メタチタン酸鉄:4.7 g/cm3)
・非毒性
The flux according to the invention satisfies the following requirements:
- presence of oxygen molecules in the gas phase of the monoxide in boiling (O 2) is the boiling point of the constant ratio (4x10 -4 cm 3) 0.1cm 3 below, sufficient heat intensity in (flux of oxygen 2500 3266K)
・ Main component of flux is low melting point (below the melting point of steel (1638 ~ 1673K))
・ The specific gravity of each component of the flux should be close (iron olivine: 4.3 g / cm 3 , iron metatitanate: 4.7 g / cm 3 )
・ Non-toxic
フラックスの組成要素の組成比の違いによる、従来法によるTIG溶接と、従来技術によるフラックスを用いたTIG溶接における溶接部の幾何学的サイズの違いについて研究し、その効果とフラックスの最適な組成要素を評価した。実験は、5mmと10mm厚の鋼プレート08Kh18N10T(オーステナト系ステンレス鋼)と鋼20のプレート(低炭素鋼)を用い、以下の条件で行った。 Study the difference in the geometric size of the weld between TIG welding by the conventional method and TIG welding using the flux by the conventional technology due to the difference in the composition ratio of the composition element of the flux, and the effect and the optimum composition element of the flux Evaluated. The experiment was performed using 5 mm and 10 mm thick steel plate 08Kh18N10T (austenato stainless steel) and steel 20 plate (low carbon steel) under the following conditions.
・溶接電流:100〜200 A
・アーク長:1.5 mm
・溶接速度:2 mm/s
フラックスをFe2SiO4、Fe2TiO4、FeTiO3、FeTi2O5の混合物とし、各要素の割合を0〜100%(10%刻みで)で変化させる
・ Welding current: 100 to 200 A
・ Arc length: 1.5 mm
・ Welding speed: 2 mm / s
The flux is a mixture of Fe 2 SiO 4 , Fe 2 TiO 4 , FeTiO 3 , FeTi 2 O 5 , and the ratio of each element is changed at 0 to 100% (in 10% increments).
実験後、溶接部をセクションごとに区切り、そのサイズを測定した。実験結果を下記の表1に示す。
・二酸化ケイ素 SiO2 2,0
・メタケイ酸鉄Fe2SiO4
オルトチタン酸鉄Fe2TiO4
メタチタン酸鉄FeTiO3
ディチタン酸鉄FeTi2O5 98,0
・ Silicon dioxide SiO 2 2,0
・ Iron metasilicate Fe 2 SiO 4
Iron orthotitanate Fe 2 TiO 4
Iron metatitanate FeTiO 3
Iron dititanate FeTi 2 O 5 98,0
Claims (1)
メタケイ酸鉄(Fe 2 SiO 4 )とオルトチタン酸鉄(Fe 2 TiO 4 )のみから構成される鉄混合物(98.0 重量%)か、
メタケイ酸鉄(Fe 2 SiO 4 )、オルトチタン酸鉄(Fe 2 TiO 4 )、及びメタチタン酸鉄(FeTiO 3 )のみから構成される鉄混合物(98.0 重量%)か、
又は、メタケイ酸鉄(Fe 2 SiO 4 )、オルトチタン酸鉄(Fe 2 TiO 4 )、メタチタン酸鉄及びディチタン酸鉄(FeTi 2 O 5 )のみから構成される鉄混合物(98.0 重量%)により構成されることを特徴とする、
鋼用タングステンイナートガスアーク溶接用活性フラックス。 Silicon dioxide (SiO 2 ) ( 2.0 wt% ),
An iron mixture (98.0% by weight) composed only of iron metasilicate (Fe 2 SiO 4 ) and iron orthotitanate (Fe 2 TiO 4 ),
An iron mixture (98.0 wt%) composed solely of iron metasilicate (Fe 2 SiO 4 ), iron orthotitanate (Fe 2 TiO 4 ), and iron metatitanate (FeTiO 3 ),
Or composed of iron mixture (98.0 wt%) consisting only of iron metasilicate (Fe 2 SiO 4 ), iron orthotitanate (Fe 2 TiO 4 ), iron metatitanate and iron dititanate (FeTi 2 O 5 ) It is characterized by being
Active flux for tungsten inert gas arc welding for steel.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| UAA200808446 | 2008-06-24 | ||
| UA200808446 | 2008-06-24 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010005696A JP2010005696A (en) | 2010-01-14 |
| JP5560504B2 true JP5560504B2 (en) | 2014-07-30 |
Family
ID=41586761
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008232932A Active JP5560504B2 (en) | 2008-06-24 | 2008-09-11 | Tungsten inert gas arc welding flux for steel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP5560504B2 (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101637471B1 (en) * | 2014-10-30 | 2016-07-07 | 현대종합금속 주식회사 | Flux cored wire for Gas shielded arc welding |
| WO2020212734A1 (en) * | 2019-04-17 | 2020-10-22 | Arcelormittal | A method for the manufacture of an assembly by tungsten inert gas (tig) welding |
| WO2020212736A1 (en) * | 2019-04-17 | 2020-10-22 | Arcelormittal | A method for the manufacture of an assembly by laser welding |
| WO2020212735A1 (en) * | 2019-04-17 | 2020-10-22 | Arcelormittal | A method for the manufacture of an assembly by submerged arc welding (saw) |
| WO2020212737A1 (en) * | 2019-04-17 | 2020-10-22 | Arcelormittal | A method for the manufacture of a coated metallic substrate by laser metal deposition |
| ES3014279T3 (en) * | 2020-10-21 | 2025-04-21 | Verdicio Solutions A I E | A method for the manufacture of a welded joint by laser arc hybrid welding |
| US20230373038A1 (en) * | 2020-10-21 | 2023-11-23 | Verdicio Solutions A.I.E. | A method for the manufacture of a welded joint by Narrow Gap Welding |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62156097A (en) * | 1985-12-27 | 1987-07-11 | Nippon Steel Corp | Low hydrogen type covered electrode |
| JPS62238093A (en) * | 1986-04-05 | 1987-10-19 | Nippon Steel Corp | Core wire for coated electrode |
-
2008
- 2008-09-11 JP JP2008232932A patent/JP5560504B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| JP2010005696A (en) | 2010-01-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5560504B2 (en) | Tungsten inert gas arc welding flux for steel | |
| JP6262240B2 (en) | Low manganese gas shielded flux cored welding electrode | |
| JP5209893B2 (en) | Ni-based alloy flux cored wire | |
| JP2011140064A (en) | Ni-BASED ALLOY FLUX-CORED WIRE | |
| CN103659043B (en) | CO 2gas shield high speed flat fillet weld series connection double-wire type combination welding wire | |
| EP4056312A1 (en) | Fluxed core wire and method for manufacturing weld joint | |
| JP2015217393A (en) | Flux-cored wire for carbon dioxide gas shielded arc welding | |
| CN103302418B (en) | Flux-cored wire and its gas-shielded arc welding method of use | |
| CA2919614A1 (en) | Flux for submerged arc welding | |
| KR101311794B1 (en) | Covered electrode for nickel based high chromium alloy welding | |
| JP2002361486A (en) | Flux cored wire for gas-shielded arc welding | |
| CN102785041A (en) | All-position flux-cored wire for alkaline gas protection | |
| CN100460127C (en) | High Speed Method for Gas Metal Arc Welding | |
| JP6599807B2 (en) | Flux-cored wire for carbon dioxide shielded arc welding | |
| JP2014014830A (en) | Welding method for duplex stainless steel | |
| EP0067494B1 (en) | Welding electrode | |
| CN104874942B (en) | Flux-cored wire and its application in vertical upward automatic vehicle welding | |
| JP3511366B2 (en) | Flux-cored wire for gas-shielded arc welding for galvanized steel sheet welding | |
| JP5600262B2 (en) | Arc brazing shielding gas and welding method using the shielding gas | |
| JPH0131996B2 (en) | ||
| JP5348937B2 (en) | Low hydrogen coated arc welding rod | |
| JP2005088039A (en) | Titania-based flux cored wire | |
| JPH0994694A (en) | Flux cored wire for stainless steel | |
| JPH0122080B2 (en) | ||
| JPH0249832B2 (en) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20110805 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130702 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20130920 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20130926 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20131018 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20131023 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20131126 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20131129 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20131209 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20140218 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140317 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140416 |
|
| A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20140421 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20140520 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20140523 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 5560504 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |