JPH06279981A - Method for carburizing steel parts to high carbon state with gas - Google Patents
Method for carburizing steel parts to high carbon state with gasInfo
- Publication number
- JPH06279981A JPH06279981A JP9541693A JP9541693A JPH06279981A JP H06279981 A JPH06279981 A JP H06279981A JP 9541693 A JP9541693 A JP 9541693A JP 9541693 A JP9541693 A JP 9541693A JP H06279981 A JPH06279981 A JP H06279981A
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- Prior art keywords
- furnace
- gas
- carbon
- temperature
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Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、鋼部品の高炭素浸炭方
法に関し、ス−ティングの発生を抑え、浸炭時間の短縮
化及び炉の保全性の向上を図り、さらに省エネルギ−効
果を有し、経済的であることを特徴とする。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a high carbon carburizing method for steel parts, which suppresses the occurrence of sooting, shortens the carburizing time and improves the maintainability of the furnace, and further has an energy saving effect. And is economical.
【0002】[0002]
【従来の技術】耐ピッチング性や、耐摩耗性などの機械
的性質を向上させるために、最近では機械部品に高炭素
浸炭を適用することが多くなってきている。該高炭素浸
炭は、浸炭時のカ−ボンポテンシャルを上げ、マルテン
サイトの生成とともにマルテンサイトよりも硬い炭化物
(カ−バイド)を析出させるものであり、該炭化物を微
細に析出させるためには、浸炭初期の段階で炭化物の核
を十分に多く生成させることが必要である。2. Description of the Related Art In order to improve mechanical properties such as pitting resistance and wear resistance, high carbon carburization has recently been often applied to mechanical parts. The high-carbon carburizing is to raise the carbon potential during carburization and to precipitate carbides (carbides) harder than martensite with the formation of martensite. In order to finely precipitate the carbides, It is necessary to generate a sufficient amount of carbide nuclei in the initial stage of carburization.
【0003】従来、そのために温度を下げて浸炭し、核
を生成させたり、若しくは一度常温まで冷却して再加熱
焼入れで炭化物を微細する等の方法が採られていた。し
かしながら、キャリアガスを使用する従来の方法では浸
炭時のカ−ボンポテンシャルの上げ幅にも限界があり、
処理に長時間を要し、さらにス−ティングによる煤の大
量発生等の問題があった。Conventionally, therefore, there has been adopted a method of lowering the temperature to carburize to generate nuclei, or to once cool to normal temperature and reheat and quench to finely refine the carbide. However, the conventional method using a carrier gas has a limit in the amount of increase in carbon potential during carburization,
It took a long time for the treatment, and there was a problem that a large amount of soot was generated due to the sooting.
【0004】[0004]
【発明が解決しようとする課題】前記の従来の方法で
は、処理パタ−ンの複雑化や処理の長時間化の問題が残
され、さらに高Cr合金鋼(Cr≒2.5%)の場合に
はCrの含有量が多いことにより、表面にCrの酸化物
が生成され、非常に厚い粒界酸化層が発生し、該粒界酸
化層が焼入れの際に表面異常層を生成して疲労強度に悪
影響を及ぼすという問題が残されていた。In the above-mentioned conventional method, the problems of complicated processing pattern and long processing time remain, and in the case of high Cr alloy steel (Cr≈2.5%). Since the Cr content is high, Cr oxides are generated on the surface, a very thick grain boundary oxide layer is generated, and the grain boundary oxide layer forms an abnormal surface layer during quenching and causes fatigue. The problem of adversely affecting strength remained.
【0005】さらにまた、表面炭素量を通常浸炭の0.
8〜1.0%より多い2〜3%とするものであるため、
炉内雰囲気のカ−ボンポテンシャルを、その処理温度で
のオ−ステナイトのカ−ボン固溶限(Acm線)より上
げなければならないが、キャリアガス(RXガス)を使
用する場合には困難が伴い、さらにス−ティングによる
煤の大量発生により、炉内雰囲気のコントロ−ルが困難
になり、さらに炉内耐火物や金属が浸食されて浸炭炉の
耐久性を損ねる等、炉の保全性にも問題が残されてい
た。Furthermore, the amount of surface carbon is usually 0.
Since it is 2 to 3%, which is more than 8 to 1.0%,
The carbon potential of the furnace atmosphere must be raised above the carbon solid solution limit (Acm line) of austenite at the processing temperature, but it is difficult when using a carrier gas (RX gas). Along with this, the soot generation due to sooting makes it difficult to control the atmosphere in the furnace, and the refractory materials and metals in the furnace are eroded to deteriorate the durability of the carburizing furnace. There was still a problem.
【0006】本発明は前記事情に鑑み、二酸化炭素の利
用と原料ガスを直接炉内に供給する処理法(以下単に、
直接浸炭法という。)を採用することにより、ス−ティ
ングを最小限に抑えながら、カ−ボンポテンシャルを上
げ、浸炭時間の短縮及び炉の保全性の向上を図り、さら
に省エネルギ−効果を有し、経済的であり、さらにまた
高Cr合金鋼に関しては、その粒界酸化の成長を抑える
ことができるものである。In view of the above circumstances, the present invention uses a carbon dioxide and a treatment method of directly supplying a raw material gas into a furnace (hereinafter, simply referred to as
It is called the direct carburizing method. ) Is adopted, the carbon potential is increased, the carburizing time is shortened and the maintainability of the furnace is improved while minimizing the sooting. Furthermore, it has an energy saving effect and is economical. In addition, regarding the high Cr alloy steel, the growth of the grain boundary oxidation can be suppressed.
【0007】[0007]
【問題を解決しようとする手段】前記課題を解決するた
め、本発明では二酸化炭素の利用と、原料ガスを直接炉
内に供給する処理法が採用される。すなわち、本発明は
炉内ガスを二酸化炭素で置き換え、且つ二酸化炭素雰囲
気で被処理品の昇温を行い、昇温完了とともに炭化水素
ガスを炉内に供給し、炉内のカ−ボンポテンシャルをそ
の温度でのカ−ボン固溶限より高い状態にコントロ−ル
して浸炭処理を行うものである。In order to solve the above problems, the present invention employs a method of using carbon dioxide and a treatment method of directly supplying a raw material gas into a furnace. That is, the present invention replaces the in-furnace gas with carbon dioxide, and raises the temperature of the article to be treated in a carbon dioxide atmosphere, and when the temperature rise is completed, the hydrocarbon gas is fed into the furnace to increase the carbon potential in the furnace. The carburizing treatment is performed by controlling to a temperature higher than the solid solubility limit of carbon at that temperature.
【0008】[0008]
【作用】本発明では、被処理品を炉内に装入後、炉内に
二酸化炭素を導入し、炉内の窒素ガス等をパ−ジし、同
時に定量の二酸化炭素を供給しながら被処理品の昇温を
行う。この工程は被処理品の温度が低いうちに原料ガス
である炭化水素ガスを供給するとス−ティングの原因と
なるため、それを避けるものである。In the present invention, after the object to be treated is charged into the furnace, carbon dioxide is introduced into the furnace, the nitrogen gas in the furnace is purged, and at the same time a fixed amount of carbon dioxide is supplied to the object to be treated. The temperature of the product is raised. In this step, if the hydrocarbon gas as the raw material gas is supplied while the temperature of the article to be treated is low, it causes the sooting, so that it is avoided.
【0009】そして、昇温完了とともに原料ガスの炭化
水素ガスを炉内に供給して炉内のカ−ボンポテンシャル
をその温度でのカ−ボン固溶限(Acm)より高い状態
にコントロ−ルして浸炭を行うものである。なお、前記
昇温完了までの間は攪拌ファンは停止させ、早期昇温を
図ることが望ましい。When the temperature rise is completed, a hydrocarbon gas as a raw material gas is supplied into the furnace to control the carbon potential in the furnace to a state higher than the carbon solid solution limit (Acm) at that temperature. Then, carburization is performed. It is desirable that the stirring fan be stopped until the temperature rise is completed to achieve early temperature rise.
【0010】前記のごとく、酸化性ガスとして二酸化炭
素ガスを考えた場合、原料ガスの炭化水素ガスとの炉内
での反応は下記式1になると考えられる。As described above, when carbon dioxide gas is considered as the oxidizing gas, the reaction of the raw material gas with the hydrocarbon gas in the furnace is considered to be the following formula 1.
【0011】[0011]
【化1】 いま、炭化水素ガスとして代表的なCH4 を考える
と、下記式2になる。[Chemical 1] Now, when CH 4 which is a typical hydrocarbon gas is considered, the following formula 2 is obtained.
【0012】[0012]
【化2】 この反応の自由エネルギ−は下記のごとくである。 △G=239580−51.26TlogT−109.
07T[J/mol] 前記式2の反応は低温領域では右側に進みにくくなり、
高温領域に移行するほど右側に進み易くなる。いま、反
応の平衡定数Kpを考えると、700℃では、Kp=
6.9に対し、930℃では、Kp=5.9×109
と極めて大きく温度に依存していることがわかる。[Chemical 2] The free energy of this reaction is as follows. ΔG = 239580-51.26TlogT-109.
07T [J / mol] In the low temperature region, the reaction of the above formula 2 hardly proceeds to the right,
As the temperature shifts to the high temperature region, it becomes easier to proceed to the right. Now, considering the equilibrium constant Kp of the reaction, at 700 ° C., Kp =
In contrast to 6.9, at 930 ° C., Kp = 5.9 × 10 9
It can be seen that it is extremely dependent on temperature.
【0013】したがって、被処理品を炉内に装入し、炉
内雰囲気温度が低下している時に、炉内に炭化水素ガス
を導入することは、炉内のCO濃度を増加させるのでは
なく、逆にクラッキングによるス−ティングを引き起こ
す要因となるものである。Therefore, introducing the hydrocarbon gas into the furnace when the article to be treated is charged into the furnace and the atmospheric temperature in the furnace is lowered, not to increase the CO concentration in the furnace. On the contrary, it is a factor that causes suiting due to cracking.
【0014】[0014]
【実施例】図1には本発明の代表的な処理パタ−ンが示
されている。すなわち、炉内に被処理品を装入(a点)
した後、炉内パ−ジ用ガスとして二酸化炭素を例えば、
1分間10〜100リットル供給して炉内の窒素ガス等
をパ−ジする。さらに、同時にその後の浸炭処理に必要
な量の酸化性ガスとしての二酸化炭素を定量、例えば、
1分間に0.5〜5リトッル供給し続ける。DESCRIPTION OF THE PREFERRED EMBODIMENT FIG. 1 shows a typical processing pattern of the present invention. That is, the product to be treated is charged into the furnace (point a)
After that, carbon dioxide as a gas for purging in the furnace, for example,
Supply 10 to 100 liters for 1 minute to purge nitrogen gas and the like in the furnace. Furthermore, at the same time, quantification of the amount of carbon dioxide as an oxidizing gas required for the subsequent carburizing treatment, for example,
Continue to deliver 0.5-5 liters per minute.
【0015】その後、炉内ガスの置き換え完了とともに
前記炉内パ−ジ用ガスとしての二酸化炭素の供給を止
め、前記定量の二酸化炭素のみを供給しながら昇温を行
い、昇温完了とともに炭化水素ガスを、例えば、1分間
に0.5〜5リットル供給し、同時に攪拌ファンを駆動
させて所定時間の処理を行うものである。Then, when the replacement of the gas in the furnace is completed, the supply of carbon dioxide as the gas for purging in the furnace is stopped, and the temperature is raised while supplying only the fixed amount of carbon dioxide. For example, 0.5 to 5 liters of gas is supplied per minute, and at the same time, the stirring fan is driven to perform processing for a predetermined time.
【0016】前記処理パタ−ンにしたがって、下記被処
理品を処理した。該被処理品の化学組成は下記表1の通
りである。The following products were processed according to the above processing pattern. The chemical composition of the article to be treated is shown in Table 1 below.
【0017】[0017]
【表1】 また、具体的浸炭処理条件は、処理温度:930℃、処
理時間:16時間であり、その後660℃まで降温した
後、850℃まで温度を上昇させ1時間保持し、油中に
焼入れしたものである。図2には得られた処理品の硬さ
分布が示され、図3にはその断面組織を示す顕微鏡写真
(×400)が示されている。[Table 1] The concrete carburizing conditions are as follows: treatment temperature: 930 ° C., treatment time: 16 hours, after that the temperature is lowered to 660 ° C., the temperature is raised to 850 ° C., the temperature is held for 1 hour, and the steel is quenched in oil. is there. FIG. 2 shows the hardness distribution of the obtained treated product, and FIG. 3 shows a micrograph (× 400) showing its cross-sectional structure.
【0018】図4には、前記同様の被処理品を、従来の
方法、すなわち、RXガスを用いて880℃で25時間
浸炭し、その後前記実施例と同様に、660℃まで降温
し、さらに850℃まで温度を上昇させ1時間保持し、
油中に焼入れした処理品の硬さ分布が示され、図5には
その断面組織を示す顕微鏡写真(×400)が示されて
いる。In FIG. 4, an article to be treated similar to the above is carburized by a conventional method, that is, using RX gas at 880 ° C. for 25 hours, and then cooled to 660 ° C. as in the above example, and Raise the temperature to 850 ° C and hold for 1 hour,
The hardness distribution of the treated product quenched in oil is shown, and FIG. 5 shows a micrograph (× 400) showing its cross-sectional structure.
【0019】両者を比較すると、組織及び硬さ分布の点
ではほぼ同様であるが、処理時間において、従来の方法
では25時間を要するのに対して、本発明では16時間
ですみ、本発明の方法によれば、浸炭用ガス及び電気エ
ネルギ−を大幅に節約できたものである。Comparing the two, although the structures and hardness distributions are almost the same, the processing time required for the conventional method is 25 hours, whereas the processing time for the present invention is 16 hours. According to the method, the carburizing gas and the electric energy can be largely saved.
【0020】また、図6には前記本発明で得られた処理
品の断面組成像写真(×1500)が示され、図7には
本発明を採用しないで直接浸炭法にて930℃で16時
間浸炭して得られた被処理品の断面組成像写真(×15
00)が示されている。Further, FIG. 6 shows a cross-sectional composition image photograph (× 1500) of the treated product obtained in the present invention, and FIG. 7 shows a direct carburizing method at 930 ° C. at 16 ° C. without adopting the present invention. Cross-sectional composition image photograph (× 15)
00) is shown.
【0021】すなわち、炉内に被処理品を装入し、約2
0分を経過した後(昇温完了前)に酸化性ガスとしての
定量の二酸化炭素(1分間に0.5〜5リットル)と炭
化水素ガス(1分間に0.5〜5リットル)を供給し、
同時に攪拌ファンを駆動させて所定処理温度までの昇温
を行い、所定時間の処理を行ったものである。That is, the article to be treated is charged into the furnace and
After a lapse of 0 minutes (before completion of temperature rise), a fixed amount of carbon dioxide (0.5 to 5 liters per minute) and a hydrocarbon gas (0.5 to 5 liters per minute) as an oxidizing gas are supplied. Then
At the same time, the stirring fan is driven to raise the temperature to a predetermined processing temperature and the processing is performed for a predetermined time.
【0022】両者を比較すると、本発明で得られた図6
の処理品の粒界酸化は10〜15μm程度で成長が止ま
っているが、図7の処理品の粒界酸化は40μm以上に
成長していて、しかもネットワ−ク状に発達しており、
本発明の方法によれば粒界酸化の成長抑制効果があるこ
とが判明したものである。Comparing both, FIG. 6 obtained by the present invention.
Although the grain boundary oxidation of the treated product of No. 10 stops growing at about 10 to 15 μm, the grain boundary oxidation of the treated product of FIG. 7 grows to 40 μm or more, and further develops like a network.
The method of the present invention has been found to have the effect of suppressing the growth of grain boundary oxidation.
【0023】[0023]
【発明の効果】本発明の方法によれば、浸炭初期におい
て比較的高いカ−ボンポテンシャルを得ることができ、
また使用浸炭ガス量も従来のRXガスの使用法に比べ少
なく、しかも炉内昇温後に供給するためス−ティングの
発生が少なく、炉の保全性を向上させることができ、同
時に浸炭時間の短縮により省エネルギ−且つ経済的であ
る効果が得られる。さらに高Cr合金鋼に関して浸炭の
際の粒界酸化の成長が抑えられる効果も得ることができ
る。According to the method of the present invention, a relatively high carbon potential can be obtained in the initial carburization.
In addition, the amount of carburizing gas used is smaller than that of the conventional method of using RX gas, and since it is supplied after the temperature inside the furnace is raised, sooting is less likely to occur and the maintainability of the furnace can be improved, and at the same time the carburizing time is shortened. As a result, it is possible to obtain the effect of being energy-saving and economical. Furthermore, it is possible to obtain the effect of suppressing the growth of grain boundary oxidation during carburization for high Cr alloy steel.
【図1】本発明の代表的な処理パタ−ン図である。FIG. 1 is a typical processing pattern diagram of the present invention.
【図2】本発明の方法による処理品の硬さ分布図であ
る。FIG. 2 is a hardness distribution chart of a product treated by the method of the present invention.
【図3】本発明の方法による処理品の断面組織を示す顕
微鏡写真(×400)である。FIG. 3 is a photomicrograph (× 400) showing a cross-sectional structure of a product treated by the method of the present invention.
【図4】従来の方法による処理品の硬さ分布図である。FIG. 4 is a hardness distribution chart of a processed product by a conventional method.
【図5】従来の方法による処理品の断面組織を示す顕微
鏡写真(×400)である。FIG. 5 is a micrograph (× 400) showing a cross-sectional structure of a processed product according to a conventional method.
【図6】本発明の方法による処理品の組成像写真(×1
500)である。FIG. 6 is a composition image photograph (× 1) of a product treated by the method of the present invention.
500).
【図7】従来の直接浸炭法による処理品の組成像写真
(×1500)である。FIG. 7 is a composition image photograph (× 1500) of a product treated by a conventional direct carburizing method.
Claims (1)
二酸化炭素雰囲気で被処理品の昇温を行い、昇温完了と
ともに炭化水素ガスを炉内に供給し、炉内のカ−ボンポ
テンシャルをその温度でのカ−ボン固溶限よりも高い状
態にコントロ−ルして浸炭することを特徴とする鋼部品
のガス高炭素浸炭方法。1. The furnace gas is replaced with carbon dioxide, and the temperature of the article to be treated is raised in a carbon dioxide atmosphere. When the temperature rise is completed, hydrocarbon gas is supplied into the furnace to increase the carbon potential in the furnace. A gas high carbon carburizing method for steel parts, characterized by controlling to a temperature higher than the solid solubility limit of carbon at that temperature and carburizing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5095416A JP2983793B2 (en) | 1993-03-30 | 1993-03-30 | Gas high carbon carburizing method for steel parts |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5095416A JP2983793B2 (en) | 1993-03-30 | 1993-03-30 | Gas high carbon carburizing method for steel parts |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06279981A true JPH06279981A (en) | 1994-10-04 |
JP2983793B2 JP2983793B2 (en) | 1999-11-29 |
Family
ID=14137087
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5095416A Expired - Lifetime JP2983793B2 (en) | 1993-03-30 | 1993-03-30 | Gas high carbon carburizing method for steel parts |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2983793B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000328224A (en) * | 1999-05-24 | 2000-11-28 | Toho Gas Co Ltd | Gas carburization method |
-
1993
- 1993-03-30 JP JP5095416A patent/JP2983793B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000328224A (en) * | 1999-05-24 | 2000-11-28 | Toho Gas Co Ltd | Gas carburization method |
Also Published As
Publication number | Publication date |
---|---|
JP2983793B2 (en) | 1999-11-29 |
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