JPH06345676A - Crystallizer for producing phenolic compound or the like - Google Patents

Crystallizer for producing phenolic compound or the like

Info

Publication number
JPH06345676A
JPH06345676A JP14101293A JP14101293A JPH06345676A JP H06345676 A JPH06345676 A JP H06345676A JP 14101293 A JP14101293 A JP 14101293A JP 14101293 A JP14101293 A JP 14101293A JP H06345676 A JPH06345676 A JP H06345676A
Authority
JP
Japan
Prior art keywords
crystallizer
scraper
molecular weight
phenols
treated
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.)
Granted
Application number
JP14101293A
Other languages
Japanese (ja)
Other versions
JP3459441B2 (en
Inventor
Keizo Takegami
敬三 竹上
Hideki Suda
英希 須田
Masahiro Kodama
正宏 児玉
Hideki Nouboshi
英喜 能星
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Idemitsu Petrochemical Co Ltd
Tsukishima Kikai Co Ltd
Original Assignee
Idemitsu Petrochemical Co Ltd
Tsukishima Kikai Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Idemitsu Petrochemical Co Ltd, Tsukishima Kikai Co Ltd filed Critical Idemitsu Petrochemical Co Ltd
Priority to JP14101293A priority Critical patent/JP3459441B2/en
Publication of JPH06345676A publication Critical patent/JPH06345676A/en
Application granted granted Critical
Publication of JP3459441B2 publication Critical patent/JP3459441B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Lubricants (AREA)

Abstract

PURPOSE:To provide the subject crystallizer capable of preventing worn powder from contamination into and foreign substances from dissolution into a liquor to be treated, thus enabling high-quality phenolic compound or bisphenol compound to be produced smoothly and assuredly. CONSTITUTION:Ultrahigh molecular weight polyethylene is used for the scraping edge 23 of a scraper 20 to come into contact with the heat transfer surface of a crystallizer body; thereby, worn powder from the scraping edge 23 is prevented from contaminating into a liquor to be treated and the components of the scraping edge 23 from dissolving into the liquor.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、フェノール類、ビスフ
ェノール類を製造する際に使用する晶出機に関する。
FIELD OF THE INVENTION The present invention relates to a crystallizer used for producing phenols and bisphenols.

【0002】[0002]

【従来の技術】従来、間接冷却式の晶出機としては、図
3に示すように、円筒状の晶出機本体1の外周にジャケ
ット2が設けられ、このジャケット2の下部及び上部に
冷媒入口3及び冷媒出口4がそれぞれ設けられ、かつ上
記晶出機本体1の内部中心に駆動軸5が回転自在に設け
られると共に、この駆動軸5に内部インペラー6、ドラ
フトチューブ7、外部インペラー8及びスクレパー9が
一体的に取り付けられる一方、上記晶出機本体1の上端
面に、上記駆動軸5を回転させる駆動機10が連結され
ているものが知られている。そして、このように構成さ
れた晶出機にあっては、上記晶出機本体1の内部に被処
理物を収容し、かつ冷媒を冷媒入口3からジャケット2
内に供給し冷媒出口4から取り出すことにより、晶出機
本体1の内部を間接冷却すると共に、駆動機10によっ
て駆動軸5を回転させ、内部インペラー6、ドラフトチ
ューブ7及び外部インペラー8によって内部の被処理物
を循環させることにより、晶出機本体1の内部の被処理
物を均一な状態に混合する一方、晶出機本体1の内周面
(冷却面)に付着した結晶を上記スクレパー9によって
掻き取ることにより、冷却面への結晶の付着による冷却
能力の低下を防ぐようにしている。
2. Description of the Related Art Conventionally, as an indirect cooling type crystallizer, as shown in FIG. 3, a jacket 2 is provided on the outer periphery of a cylindrical crystallizer main body 1, and a refrigerant is provided on the lower and upper parts of the jacket 2. An inlet 3 and a refrigerant outlet 4 are respectively provided, and a drive shaft 5 is rotatably provided at the inner center of the crystallizer main body 1, and an inner impeller 6, a draft tube 7, an outer impeller 8 and It is known that the scraper 9 is integrally attached, while the drive machine 10 for rotating the drive shaft 5 is connected to the upper end surface of the crystallizer main body 1. In the crystallizer configured as described above, the object to be treated is housed inside the crystallizer main body 1, and the refrigerant is introduced from the refrigerant inlet 3 into the jacket 2
The inside of the crystallizer main body 1 is indirectly cooled by being supplied into the inside of the crystallizer outlet 4, and the drive shaft 5 is rotated by the driving machine 10, and the inside of the crystallizer main body 1 is rotated by the internal impeller 6, the draft tube 7 and the external impeller 8. By circulating the object to be treated, the object to be treated inside the crystallizer main body 1 is mixed uniformly, while the crystals attached to the inner peripheral surface (cooling surface) of the crystallizer main body 1 are scraped by the scraper 9 By scraping off with a scraper, it is possible to prevent a decrease in the cooling capacity due to the adhesion of crystals to the cooling surface.

【0003】[0003]

【発明が解決しようとする課題】ところで、上記間接冷
却式の晶出機のスクレパー9の材質としては、金属か樹
脂が使用されている。このうち、金属製のスクレパー9
の場合には、スクレパー9を晶出機本体1の冷却面に接
触させることはできず、従って、該冷却面とスクレパー
9との間に若干の隙間があるため、冷却面に付着した結
晶を完全に除去することができず、この除去できない付
着結晶が伝熱抵抗となり、大きな伝熱係数が得られない
という問題がある。一方、樹脂製のスクレパー9は冷却
面に接触させて操作できるために高伝熱係数が得られる
が、耐摩耗性、耐溶剤性に優れていること及び樹脂から
の溶出がないこと等の条件を満足しなければならない。
特に、ビスフェノールのように高品質を要求される物質
の場合、摩耗粉や樹脂からの溶出成分によって製品品質
に悪影響を及ぼすことを避けなければならない。この点
に関して、従来上記スクレパーの材質として多用されて
いるMCナイロンは、耐摩耗性に優れているものの、フ
ェノール類、ビスフェノール類に対しては、MCナイロ
ンそのものが溶解してしまうため使用できない。このた
め、フェノール類、ビスフェノール類に耐性を持ち耐摩
耗性に優れている材料として、フェノール樹脂が使用さ
れている。しかしながら、このフェノール樹脂において
は、微量であるが有色の摩耗粉が発生し最終製品に異物
として混入するという問題がある。また、フェノール樹
脂から若干の浸出成分があり、これが被処理液を着色し
て最終製品を着色させてしまうという問題がある。
By the way, as the material of the scraper 9 of the indirect cooling type crystallizer, metal or resin is used. Of these, the metal scraper 9
In the case of, the scraper 9 cannot be brought into contact with the cooling surface of the crystallizer main body 1, and therefore, since there is a slight gap between the cooling surface and the scraper 9, the crystals attached to the cooling surface can be removed. There is a problem that it cannot be completely removed, and the adhered crystal that cannot be removed becomes a heat transfer resistance and a large heat transfer coefficient cannot be obtained. On the other hand, the resin scraper 9 can obtain a high heat transfer coefficient because it can be operated by bringing it into contact with the cooling surface. Must be satisfied.
In particular, in the case of a substance that requires high quality such as bisphenol, it is necessary to avoid adversely affecting the product quality due to abrasion powder and components eluted from the resin. In this regard, MC nylon, which has been widely used as a material for the scraper in the related art, has excellent wear resistance, but cannot be used for phenols and bisphenols because MC nylon itself dissolves. Therefore, a phenol resin is used as a material having resistance to phenols and bisphenols and excellent in abrasion resistance. However, this phenolic resin has a problem that a small amount of colored abrasion powder is generated and mixed into the final product as a foreign substance. Further, there is a problem that some leaching components are present from the phenol resin, which causes the liquid to be treated to be colored and the final product to be colored.

【0004】本発明は、上記事情に鑑みてなされたもの
で、その目的とするところは、フェノール類、ビスフェ
ノール類を製造する際に、晶出機本体の伝熱面やスケー
ル付着面等に接触するスクレパーや攪拌機の回転軸のよ
うな摺動部に超高分子量ポリエチレンを使用することに
より、被処理液への摩耗粉の混入や異物の溶出等を防止
できて、高品質のフェノール類、ビスフェノール類を円
滑にかつ確実に製造することができるフェノール類等製
造用晶出機を提供することにある。
The present invention has been made in view of the above circumstances, and an object thereof is to contact a heat transfer surface or a scale adhering surface of a crystallizer main body during the production of phenols and bisphenols. By using ultra-high molecular weight polyethylene for sliding parts such as scrapers and rotating shafts of stirrers, it is possible to prevent abrasion powder from mixing into the liquid to be treated and elution of foreign substances, and to ensure high-quality phenols and bisphenols. It is intended to provide a crystallizer for producing phenols and the like, which can smoothly and reliably produce the same.

【0005】[0005]

【課題を解決するための手段】上記目的を達成するため
に、本発明は、フェノール類、ビスフェノール類を冷却
して晶出させるフェノール類等製造用晶出機において、
互いに接触しながら相対移動する摺動部に超高分子量ポ
リエチレンを使用するものである。さらに、耐摩耗性を
向上させるために、超高分子量ポリエチレンにグラスフ
ァイバーや液晶ポリマー等を配合させることも可能であ
る。また、超高分子量ポリエチレンの分子量は大きいほ
ど耐摩耗性が向上するが、一般的な分子量のものでも十
分である。
In order to achieve the above-mentioned object, the present invention provides a crystallizer for producing phenols or the like for crystallization by cooling phenols or bisphenols,
Ultra high molecular weight polyethylene is used for the sliding parts that move relative to each other while contacting each other. Further, in order to improve abrasion resistance, it is possible to blend glass fiber, liquid crystal polymer, or the like with ultra-high molecular weight polyethylene. Further, the higher the molecular weight of ultra-high molecular weight polyethylene, the higher the abrasion resistance, but a general molecular weight is also sufficient.

【0006】[0006]

【作用】本発明のフェノール類等製造用晶出機にあって
は、晶出機本体の伝熱面やスケール付着面等に接触する
スクレパーや攪拌機の回転軸のような摺動部に超高分子
量ポリエチレンを使用することにより、上記摺動部から
摩耗粉が被処理物に混入することを防ぎ、かつ摺動部の
成分が被処理物に溶出することを防止する。
In the crystallizer for producing phenols and the like of the present invention, the sliding portion such as the scraper or the rotating shaft of the stirrer that comes into contact with the heat transfer surface of the crystallizer body or the scale adhering surface has an ultra-high height. By using the molecular weight polyethylene, the abrasion powder is prevented from being mixed into the object to be treated from the sliding portion, and the components of the sliding portion are prevented from being eluted into the object to be treated.

【0007】[0007]

【実施例】以下、図1〜図3に基づいて本発明の実施例
を説明する。なお、本発明はその要旨を越えない限り以
下の実施例に限定されるものではない。
Embodiments of the present invention will be described below with reference to FIGS. The present invention is not limited to the following examples unless it exceeds the gist.

【0008】図1と図2は本発明を適用したスクレパー
20を示すもので、このスクレパー20は図3に示す晶
出機のスクレパー9の代わりに使用されるものである。
そして、上記スクレパー20は、ドラフトチューブ7と
の間を連結する連結部材21にスクレパー本体22が取
り付けられ、かつこのスクレパー本体22に掻取片23
が移動可能に装着されると共に、上記スクレパー本体2
2の内部に、掻取片23を晶出機本体1の内周面(冷却
面)に押し当てるスプリング24が設けられたものであ
る。また、上記掻取片23は超高分子量ポリエチレンか
ら形成されている。
FIGS. 1 and 2 show a scraper 20 to which the present invention is applied, and this scraper 20 is used in place of the scraper 9 of the crystallizer shown in FIG.
In the scraper 20, the scraper main body 22 is attached to the connecting member 21 connecting the draft tube 7 and the scraper main body 22.
And the scraper body 2
A spring 24 for pressing the scraping piece 23 against the inner peripheral surface (cooling surface) of the crystallizer main body 1 is provided inside the apparatus 2. The scraping piece 23 is made of ultra-high molecular weight polyethylene.

【0009】次に、本発明をさらに具体的に実施した場
合について説明する。 「実施例1」内径310.5mm、高さ450mmの円
筒型ステンレス製容器に攪拌軸を設け、この攪拌軸から
半径方向(4方向)に樹脂片を設け、スプリングにより
この容器の内壁面に押し付けておく。そして、この容器
に液を入れた状態で、樹脂片を内壁面に押し付けながら
攪拌軸を回転させ樹脂片が内壁面と連続的に擦れ合うよ
うにする。上記装置の4枚の樹脂片に超高分子量ポリエ
チレンを用いて以下の条件で操作を行った。 使用液 フェノール水 回転数 130rpm 温度 室温 操作時間 231時間 この操作の前後での樹脂片の重量変化は4枚の平均で−
0.05%であり、わずかな減少であった。
Next, a case in which the present invention is carried out more specifically will be described. [Example 1] A cylindrical stainless steel container having an inner diameter of 310.5 mm and a height of 450 mm was provided with a stirring shaft, resin pieces were provided in the radial direction (4 directions) from the stirring shaft, and pressed against the inner wall surface of the container by a spring. Keep it. Then, while the liquid is put in this container, the stirring shaft is rotated while pressing the resin piece against the inner wall surface so that the resin piece continuously rubs against the inner wall surface. The operation was performed under the following conditions using ultra-high molecular weight polyethylene for the four resin pieces of the above apparatus. Liquid used Phenol water Rotation speed 130 rpm Temperature Room temperature Operation time 231 hours Weight change of resin piece before and after this operation is an average of 4 pieces-
It was 0.05%, which was a slight decrease.

【0010】「実施例2」内径2.5m、高さ6mの間
接冷却式掻取型晶出機を使用したビスフェノール類の冷
却晶析操作において、掻取刃に超高分子量ポリエチレン
を使用して1年間連続使用した。この結果、掻取刃の平
均摩耗率は約5%であったが、1年間の運転中冷却晶析
性能の低下はなく、また最終製品の品質にも影響はなく
高純度ビスフェノールを継続して生産できた。
[Example 2] In a cooling crystallization operation of bisphenols using an indirect cooling type scraping crystallizer having an inner diameter of 2.5 m and a height of 6 m, ultrahigh molecular weight polyethylene was used for a scraping blade. It was used continuously for one year. As a result, the average wear rate of the scraping blade was about 5%, but there was no deterioration in cooling crystallization performance during operation for one year, and there was no effect on the quality of the final product. I was able to produce.

【0011】「比較例1」上記実施例1と同様の装置、
条件で樹脂片にフェノール樹脂を使用したところ、操作
前後での重量変化は4枚の平均で約−0.4%であり、
超高分子量ポリエチレンより大きな重量変化であった。
また、操作後の液の色が少し黄色に変色しており、樹脂
からの若干の溶出があったと考えられる。さらに液中に
黒っぽい摩耗粉が浮遊していた。
"Comparative Example 1" An apparatus similar to that of Example 1 above,
When a phenolic resin was used for the resin piece under the conditions, the weight change before and after the operation was about -0.4% on the average of four pieces,
The weight change was greater than that of ultra high molecular weight polyethylene.
Further, the color of the liquid after the operation turned a little yellow, and it is considered that there was some elution from the resin. Furthermore, blackish abrasion powder was floating in the liquid.

【0012】「比較例2」内径0.8m、高さ2mの間
接冷却式掻取型晶出機を使用したフェノール類の冷却晶
析操作において掻取刃にテフロン樹脂を使用して操作を
行ったところ、1週間で掻取刃が完全に摩耗して掻取操
作ができなくなり、冷却面に結晶が付着して伝熱性能が
低下し運転不能になった。
"Comparative Example 2" In a cooling crystallization operation of phenols using an indirect cooling type scraping crystallizer having an inner diameter of 0.8 m and a height of 2 m, a scraping blade is made of Teflon resin. As a result, in one week, the scraping blade was completely worn out and the scraping operation could not be performed, and the crystals adhered to the cooling surface to deteriorate the heat transfer performance, and the operation became impossible.

【0013】[0013]

【発明の効果】以上説明したように、本発明は、フェノ
ール類、ビスフェノール類を製造する際に、晶出機本体
の伝熱面やスケール付着面等に接触するスクレパーや攪
拌機の回転軸のような摺動部に超高分子量ポリエチレン
を使用することにより、上記摺動部から摩耗粉が被処理
物に混入することを防ぐことができ、かつ摺動部の成分
が被処理物に溶出することを防止することができると共
に、高品質のフェノール類、ビスフェノール類を円滑に
かつ確実に製造することができる。
As described above, according to the present invention, when the phenols and the bisphenols are produced, the scraper and the rotating shaft of the stirrer that come into contact with the heat transfer surface and the scale adhering surface of the crystallizer main body can be used. By using ultra high molecular weight polyethylene for the sliding part, it is possible to prevent abrasion powder from mixing into the object to be processed from the sliding part, and to elute the components of the sliding part into the object to be processed. And high quality phenols and bisphenols can be produced smoothly and reliably.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の一実施例を示すスクレパー部の側面図
である。
FIG. 1 is a side view of a scraper portion showing an embodiment of the present invention.

【図2】図1のII−II線に沿った断面図である。FIG. 2 is a sectional view taken along line II-II of FIG.

【図3】間接冷却式掻取型晶出機を示す斜視図である。FIG. 3 is a perspective view showing an indirect cooling type scraping crystallizer.

【符号の説明】[Explanation of symbols]

20 スクレパー 23 掻取片(摺動部) 20 scraper 23 scraping piece (sliding part)

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 // C10N 40:02 50:08 (72)発明者 児玉 正宏 千葉県市原市姉崎海岸1番地1 出光石油 化学株式会社内 (72)発明者 能星 英喜 千葉県市原市姉崎海岸1番地1 出光石油 化学株式会社内─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 5 Identification number Reference number in the agency FI Technical display location // C10N 40:02 50:08 (72) Inventor Masahiro Kodama 1 Iezaki Kaigan, Ichihara, Chiba 1 Within Idemitsu Petrochemical Co., Ltd. (72) Inventor Hideki Noboshi 1 Iezaki Kaigan, Ichihara-shi, Chiba 1 Idemitsu Petrochemical Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 フェノール類、ビスフェノール類を冷却
して晶出させるフェノール類等製造用晶出機において、
互いに接触しながら相対移動する摺動部に超高分子量ポ
リエチレンを使用することを特徴とするフェノール類等
製造用晶出機。
1. A crystallizer for producing phenols or the like, which crystallizes by cooling phenols or bisphenols,
A crystallizer for producing phenols and the like, characterized in that ultra-high molecular weight polyethylene is used for the sliding parts that move relative to each other while contacting each other.
JP14101293A 1993-06-11 1993-06-11 Crystallizer for production of phenols and bisphenols Expired - Lifetime JP3459441B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14101293A JP3459441B2 (en) 1993-06-11 1993-06-11 Crystallizer for production of phenols and bisphenols

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14101293A JP3459441B2 (en) 1993-06-11 1993-06-11 Crystallizer for production of phenols and bisphenols

Publications (2)

Publication Number Publication Date
JPH06345676A true JPH06345676A (en) 1994-12-20
JP3459441B2 JP3459441B2 (en) 2003-10-20

Family

ID=15282146

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14101293A Expired - Lifetime JP3459441B2 (en) 1993-06-11 1993-06-11 Crystallizer for production of phenols and bisphenols

Country Status (1)

Country Link
JP (1) JP3459441B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013056870A (en) * 2011-09-09 2013-03-28 Mitsubishi Chemicals Corp Method of producing bisphenol a

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013056870A (en) * 2011-09-09 2013-03-28 Mitsubishi Chemicals Corp Method of producing bisphenol a

Also Published As

Publication number Publication date
JP3459441B2 (en) 2003-10-20

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