JP2920688B2 - Non-reducing dielectric porcelain composition - Google Patents

Non-reducing dielectric porcelain composition

Info

Publication number
JP2920688B2
JP2920688B2 JP2311924A JP31192490A JP2920688B2 JP 2920688 B2 JP2920688 B2 JP 2920688B2 JP 2311924 A JP2311924 A JP 2311924A JP 31192490 A JP31192490 A JP 31192490A JP 2920688 B2 JP2920688 B2 JP 2920688B2
Authority
JP
Japan
Prior art keywords
mol
dielectric
composition
reducing dielectric
batio
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP2311924A
Other languages
Japanese (ja)
Other versions
JPH04184809A (en
Inventor
俊樹 西山
幸生 浜地
行進 坂部
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.)
Murata Manufacturing Co Ltd
Original Assignee
Murata Manufacturing 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 Murata Manufacturing Co Ltd filed Critical Murata Manufacturing Co Ltd
Priority to JP2311924A priority Critical patent/JP2920688B2/en
Publication of JPH04184809A publication Critical patent/JPH04184809A/en
Application granted granted Critical
Publication of JP2920688B2 publication Critical patent/JP2920688B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Compositions Of Oxide Ceramics (AREA)
  • Ceramic Capacitors (AREA)
  • Inorganic Insulating Materials (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は非還元性誘電体磁器組成物に関し、特にた
とえばニッケルなどの卑金属を内部電極とする積層コン
デンサなどの誘電体材料として好適な非還元性誘電体磁
器組成物に関する。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a non-reducing dielectric ceramic composition, and more particularly to a non-reducing dielectric ceramic composition suitable as a dielectric material for a multilayer capacitor having a base metal such as nickel as an internal electrode. The present invention relates to a conductive dielectric ceramic composition.

(従来技術) 従来の誘電体磁器材料では、中性または還元性の低酸
素分圧下で焼成すると還元され、半導体化を起こすとい
う性質を有していた。そのため、内部電極の材料として
は、誘電体磁器材料の焼結する温度で溶融せず、かつ誘
電体磁器材料を半導体化させない高い酸素分圧下で焼成
しても酸化されない、たとえばパラジウム、白金などの
貴金属を用いなければならず、製造される積層コンデン
サの低コスト化の大きな妨げとなっていた。
(Prior Art) A conventional dielectric porcelain material has the property of being reduced when baking under a neutral or reducing low oxygen partial pressure, and becoming a semiconductor. Therefore, as a material of the internal electrode, the dielectric ceramic material does not melt at the sintering temperature, and is not oxidized even when fired under a high oxygen partial pressure that does not turn the dielectric ceramic material into a semiconductor, such as palladium and platinum. Precious metals must be used, which has been a major obstacle to reducing the cost of the manufactured multilayer capacitor.

そこで、上述の問題を解決するために、たとえばニッ
ケルなどの安価な卑金属を内部電極の材料として使用す
ることが望まれていた。しかし、このような卑金属を内
部電極の材料として使用し、従来の条件下で焼成する
と、電極材料が酸化してしまい、電極としての機能を果
たさない。そのため、このような卑金属を内部電極の材
料として使用するためには、酸素分圧の低い中性または
還元性の雰囲気において焼成しても半導体化せず、コン
デンサ用の誘電体材料として十分な絶縁抵抗値と優れた
誘電特性とを有する誘電体磁器材料が必要とされてお
り、これらの条件をみたすものとして、たとえば特開昭
62-256422号公報にBaTiO3−CaZrO3−MnO−MgO系の組成
物が、特公昭61-14611号公報にBaTiO3−(Mg,Zn,Sr,C
a)O−B2O3−SiO2系の組成物が、それぞれ提案されて
いる。
Therefore, in order to solve the above problem, it has been desired to use an inexpensive base metal such as nickel as a material for the internal electrodes. However, when such a base metal is used as a material for an internal electrode and fired under conventional conditions, the electrode material is oxidized and does not function as an electrode. Therefore, in order to use such a base metal as a material for an internal electrode, it does not turn into a semiconductor even when fired in a neutral or reducing atmosphere having a low oxygen partial pressure, and has a sufficient insulating property as a dielectric material for a capacitor. There is a need for a dielectric porcelain material having resistance and excellent dielectric properties.
The composition of BaTiO 3 -CaZrO 3 -MnO-MgO system 62-256422 Patent Publication, BaTiO 3 in JP-B 61-14611 - (Mg, Zn, Sr , C
a) O—B 2 O 3 —SiO 2 based compositions have each been proposed.

(発明が解決しようとする課題) しかし、特開昭62-256422号公報に開示されている非
還元性誘電体磁器組成物では、CaZrO3や焼成過程で生成
するCaTiO3がMnなどとともに2次相を生成しやすいた
め、高温における信頼性の低下につながる危険性があ
る。
(Problems to be Solved by the Invention) However, in the non-reducing dielectric ceramic composition disclosed in Japanese Patent Application Laid-Open No. 62-256422, CaZrO 3 and CaTiO 3 generated in the firing step are secondary with Mn and the like. There is a risk that the formation of a phase is likely to reduce the reliability at high temperatures.

また、特公昭61-14611号公報に開示されている組成物
では、得られる誘電体の誘電率が2000〜2800であり、パ
ラジウムなどの貴金属を使用している従来からの磁器組
成物の誘電率3000〜3500と比較すると劣っている。した
がって、コストダウンのためにこの組成物をそのまま従
来の材料に置き換えると、小型大容量化という点で不利
であり問題が残される。
Further, in the composition disclosed in JP-B-61-14611, the dielectric constant of the obtained dielectric is 2000 to 2800, and the dielectric constant of a conventional porcelain composition using a noble metal such as palladium. Inferior to 3000-3500. Therefore, if this composition is directly replaced with a conventional material for cost reduction, it is disadvantageous in terms of increasing the size and the capacity, and the problem remains.

さらに、特公昭61-14611号公報に開示されている組成
物から得られる誘電体では、その誘電率の温度変化率
が、20℃の容量値を基準としたときに、−25℃〜+85℃
の範囲では±10%以内であるが、+85℃を超える高温で
は10%を大きく超えてしまい、EIA規格に規定されてい
るX7R特性をも大きくはずれてしまうという欠点があっ
た。
Further, in the dielectric obtained from the composition disclosed in Japanese Patent Publication No. 61-14611, the temperature change rate of the dielectric constant is -25 ° C to + 85 ° C based on the capacitance value of 20 ° C.
Within the range of ± 10%, but at temperatures higher than + 85 ° C, it greatly exceeds 10%, and there is a drawback that the X7R characteristic specified in the EIA standard is greatly deviated.

それゆえに、この発明の主たる目的は、低酸素分圧下
であっても組織が半導体化せず焼成可能であり、かつ誘
電率が3000以上、絶縁抵抗値の対数値(logIR)が11.0
以上、さらに誘電率の温度特性が25℃の容量値を基準と
したときに、−55℃〜125℃の広い範囲にわたって±15
%以内を満足する誘電体を得ることができる、非還元性
誘電体磁器組成物を提供することである。
Therefore, a main object of the present invention is that even under a low oxygen partial pressure, the structure does not become a semiconductor and can be fired, and the dielectric constant is 3000 or more, and the logarithmic value of the insulation resistance value (logIR) is 11.0.
As described above, when the temperature characteristic of the dielectric constant is based on the capacitance value of 25 ° C., ± 15 ° C. over a wide range of −55 ° C. to 125 ° C.
It is an object of the present invention to provide a non-reducible dielectric porcelain composition capable of obtaining a dielectric material satisfying the range of at most%.

(課題を解決するための手段) この発明は、不純物として含まれるアルカリ金属酸化
物の含有量が0.04重量%以下のBaTiO3と、Tb2O3,Dy2O3,
Ho2O3,Er2O3の中から選ばれた少なくとも1種の希土類
酸化物(Re2O3)およびCo2O3とを主成分とし、その配合
比は、BaTiO3が88.0〜99.4モル%、Re2O3が0.3〜6.0モ
ル%、およびCo2O3が0.3〜6.0モル%であり、主成分100
モル%に対して、副成分として、BaOを0.2〜4.0モル
%、およびMnOを0.2〜3.0モル%含有する、非還元性誘
電体磁器組成物である。
(Means for Solving the Problems) The present invention provides BaTiO 3 having an alkali metal oxide content of 0.04% by weight or less as an impurity, Tb 2 O 3 , Dy 2 O 3 ,
Ho 2 O 3, Er 2 at least one rare earth oxide selected from among O 3 (Re 2 O 3) and Co 2 O 3 and as a main component, the mixing ratio, BaTiO 3 is 88.0 to 99.4 Mol%, Re 2 O 3 is 0.3 to 6.0 mol%, and Co 2 O 3 is 0.3 to 6.0 mol%.
It is a non-reducing dielectric ceramic composition containing 0.2 to 4.0 mol% of BaO and 0.2 to 3.0 mol% of MnO as subcomponents with respect to mol%.

なお、主成分100モル%に対して、副成分として、さ
らにY2O3を3モル%以下含有してもよい。
In addition, Y 2 O 3 may be further contained as a minor component in an amount of 3 mol% or less based on 100 mol% of the main component.

この発明において、主成分および副成分の組成範囲を
上記のように限定した理由について以下に説明する。
In the present invention, the reason why the composition ranges of the main component and the subcomponent are limited as described above will be described below.

まず、主成分の組成範囲の限定理由について述べる。 First, the reasons for limiting the composition range of the main component will be described.

BaTiO3の構成比率を88.0〜99.4モル%とするのは、そ
の構成比率が88.0モル%未満の場合には、希土類酸化物
およびCo2O3の構成比率が多くなるため、絶縁抵抗値お
よび誘電率の低下が生じ、逆に99.4モル%を超えれば、
希土類酸化物およびCo2O3の添加の効果がなく、高温部
(キュリー点付近)の容量温度変化率が大きく正側には
ずれるからである。また、BaTiO3中のアルカリ金属酸化
物含有量を0.04重量%以下としたのは、これを超えて含
有すると誘電率の低下が生じるからである。
The reason why the composition ratio of BaTiO 3 is set to 88.0 to 99.4 mol% is that when the composition ratio is less than 88.0 mol%, the composition ratio of rare earth oxide and Co 2 O 3 increases, so that the insulation resistance value and the dielectric Rate decreases, and if it exceeds 99.4 mol%,
This is because there is no effect of the addition of the rare earth oxide and Co 2 O 3 , and the rate of temperature change of the capacity in the high temperature part (near the Curie point) largely deviates to the positive side. The reason why the content of the alkali metal oxide in BaTiO 3 is set to 0.04% by weight or less is that if the content exceeds this range, the dielectric constant is reduced.

次に、副成分の組成範囲の限定理由について述べる。 Next, the reasons for limiting the composition range of the accessory component will be described.

BaOは、主成分のBaとTiとのモル比を補正するために
添加されるが、その添加量を0.2〜4.0モル%とするの
は、0.2モル%未満の添加量であれば、雰囲気焼成中に
組織が半導体化し、絶縁抵抗値の著しい低下が生じるか
らであり、逆に4.0モル%を超える添加量になると、焼
結性が低下するからである。
BaO is added to correct the molar ratio of the main component Ba and Ti, but the amount of addition is 0.2 to 4.0 mol% if the addition amount is less than 0.2 mol%. This is because the structure becomes a semiconductor in the inside and the insulation resistance value is remarkably reduced. Conversely, when the added amount exceeds 4.0 mol%, the sinterability decreases.

MnOは、還元防止のために添加されるが、その添加量
を0.2〜3.0モル%とするのは、0.2モル%未満の添加量
であれば、組織の耐還元性向上に効果がなくなり、絶縁
抵抗値の著しい低下をまねくからであり、3.0モル%を
超えて添加すると、絶縁抵抗値、特に高温における抵抗
値の低下が生じるからである。
MnO is added to prevent reduction. However, the addition amount of 0.2 to 3.0 mol% is not effective in improving the reduction resistance of the tissue if the addition amount is less than 0.2 mol%. This is because a remarkable decrease in the resistance value is caused, and if added in excess of 3.0 mol%, the insulation resistance value, particularly the resistance value at high temperatures, is reduced.

なお、Y2O3は、誘電率の温度特性をよりフラットに改
善するために必要に応じて添加されるが、その添加量を
3.0モル%以下としたのは、これを超えて添加すると焼
結性が著しく劣るからである。
Y 2 O 3 is added as needed to improve the temperature characteristics of the dielectric constant more flatly.
The reason why the content is set to 3.0 mol% or less is that if added in excess of this, the sinterability is remarkably deteriorated.

(発明の効果) この発明によれば、中性、または還元雰囲気におい
て、1300〜1360℃の温度で焼成しても組織が還元されて
半導体化することなく、対数値(logIR)で11.0以上の
高い絶縁抵抗値を示すとともに、3000以上の高誘電率を
有し、かつ容量の温度変化率もEIAに規定されているX7R
特性を満足する誘電体を得ることができる、非還元性誘
電体磁器組成物を得ることができる。
(Effects of the Invention) According to the present invention, even when fired at a temperature of 1300 to 1360 ° C in a neutral or reducing atmosphere, the structure is not reduced to a semiconductor, and a logarithmic value (logIR) of 11.0 or more is obtained. X7R, which has a high insulation resistance value, a high dielectric constant of 3000 or more, and a temperature change rate of the capacitance specified by EIA
It is possible to obtain a non-reducible dielectric porcelain composition capable of obtaining a dielectric satisfying the characteristics.

そして、この発明にかかる非還元性誘電体磁器組成物
を、たとえば積層セラミックコンデンサの誘電体材料と
して用いれば、ニッケルなどで代表される卑金属を内部
電極として使用することが可能となり、従来より使用さ
れてきたパラジウムなどの貴金属を内部電極とする積層
セラミックコンデンサと比較して、特性を落とすことな
く大幅なコストダウンを行うことが可能となる。
When the non-reducing dielectric ceramic composition according to the present invention is used, for example, as a dielectric material of a multilayer ceramic capacitor, it becomes possible to use a base metal represented by nickel or the like as an internal electrode, which has been conventionally used. Compared with a laminated ceramic capacitor using a noble metal such as palladium as an internal electrode, it is possible to greatly reduce costs without deteriorating characteristics.

この発明の上述の目的,その他の目的,特徴および利
点は、以下の実施例の詳細な説明から一層明らかとなろ
う。
The above and other objects, features and advantages of the present invention will become more apparent from the following detailed description of the embodiments.

(実施例) まず、素原料として、不純物含有量の異なるBaTiO3,B
aとTiとのモル比を補正するためのBaCO3,希土類酸化物,
Cos2O3,MnOおよびY2O3を準備し、別表1に示した組成割
合になるよう秤量し、秤量物を得た。この秤量物に酢酸
ビニル系バインダを5重量%添加した後、PSZボールを
用いたボールミルで十分に湿式混合粉砕して混合物を得
た。次に、混合物中の分散媒を蒸発、乾燥させた後、整
粒の工程を経て粉末を得た。得られた粉末を2ton/cm2
圧力で直径10mm、厚さ1mmの円板状にプレス成形して成
形体を得た。
(Example) First, as raw materials, BaTiO 3 , B having different impurity contents were used.
BaCO 3 , rare earth oxide, to correct the molar ratio of a and Ti,
Cos 2 O 3 , MnO and Y 2 O 3 were prepared and weighed to have the composition ratios shown in Table 1 to obtain a weighed material. After adding 5% by weight of a vinyl acetate-based binder to the weighed material, the mixture was sufficiently wet-mixed and pulverized with a ball mill using PSZ balls to obtain a mixture. Next, after the dispersion medium in the mixture was evaporated and dried, a powder was obtained through a sizing process. The obtained powder was press-molded at a pressure of 2 ton / cm 2 into a disk having a diameter of 10 mm and a thickness of 1 mm to obtain a compact.

この成形体を、400℃の空気中で3時間保持して脱バ
インダを行った後、H2/N2の体積比率が3/100の還元雰囲
気ガス気流中において、別表2に示した温度で2時間焼
成し、磁器を得た。
After holding the compact in air at 400 ° C. for 3 hours to remove the binder, the compact was heated at a temperature shown in Table 2 in a reducing atmosphere gas stream having a H 2 / N 2 volume ratio of 3/100. It was fired for 2 hours to obtain porcelain.

得られた磁器の両面に、Agペーストを塗布、焼き付け
ることにより、電極を形成してコンデンサとし、室温で
の誘電率ε、誘電損失tanδおよび絶縁抵抗値IRと、容
量の温度変化率TCCとを測定した。その結果を、表2に
示した。
By coating and baking an Ag paste on both sides of the obtained porcelain, an electrode is formed as a capacitor, and the dielectric constant ε at room temperature, the dielectric loss tanδ and the insulation resistance value IR, and the temperature change rate TCC of the capacitance are determined. It was measured. The results are shown in Table 2.

なお、表2には、誘電率および誘電損失については、
温度25℃、周波数1kHz、交流電圧1Vの条件で測定した結
果(ε25およびtanδ)について示し、絶縁抵抗値につ
いては、温度25℃、直流電圧500Vの条件で2分間前もっ
て充電したときの測定結果を対数値(logIR25)で示
し、さらに容量の温度変化率については、25℃の容量値
(C25)を基準としたときの−55℃および125℃における
それぞれの静電容量値の変化率(−55℃:ΔC-55/C25
よび+125℃:ΔC+125/C25)と、−55℃〜+125℃の間
において容量温度変化率が最大である値の絶対値、いわ
ゆる最大変化率(Cmax:|ΔC/C25|max)とについて示し
た。
Table 2 shows the dielectric constant and dielectric loss.
The results (ε 25 and tan δ) measured under the conditions of a temperature of 25 ° C, a frequency of 1 kHz, and an AC voltage of 1 V are shown. The insulation resistance value is the result of a measurement performed at a temperature of 25 ° C and a DC voltage of 500 V for 2 minutes in advance. Is shown as a logarithmic value (logIR 25 ), and the rate of temperature change of the capacitance is the rate of change of the respective capacitance values at −55 ° C. and 125 ° C. based on the capacitance value (C 25 ) at 25 ° C. (−55 ° C .: ΔC −55 / C 25 and + 125 ° C .: ΔC +125 / C 25 ) and the absolute value of the value at which the capacitance temperature change rate is the maximum between −55 ° C. and + 125 ° C., the so-called maximum change rate (Cmax: | ΔC / C 25 | max).

表2の結果より、この発明の範囲内の試料について
は、誘電率,誘電損失,絶縁抵抗値および容量の温度変
化率において優れた特性が得られることが明らかであ
る。
From the results in Table 2, it is clear that the samples within the scope of the present invention can obtain excellent characteristics in the dielectric constant, the dielectric loss, the insulation resistance value, and the temperature change rate of the capacitance.

また、表2に示した結果は単板コンデンサにおいて得
られた結果であるが、同じ組成物をシート成形し、チッ
プ加工を行った積層コンデンサにおいても、上述の結果
とほぼ同等の結果が得られる。
The results shown in Table 2 are obtained for single-plate capacitors, but the same results are obtained for multilayer capacitors obtained by forming the same composition into sheets and performing chip processing. .

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】不純物として含まれるアルカリ金属酸化物
の含有量が0.04重量%以下のBaTiO3と、Tb2O3,Dy2O3,Ho
2O3,Er2O3の中から選ばれた少なくとも1種の希土類酸
化物(Re2O3)およびCo2O3とを主成分とし、その配合比
は、 BaTiO3が88.0〜99.4モル%、 Re2O3が0.3〜6.0モル%、および Co2O3が0.3〜6.0モル% であり、 前記主成分100モル%に対して、副成分として、 BaOを0.2〜4.0モル%、および MnOを0.2〜3.0モル% 含有する、非還元性誘電体磁器組成物。
(1) BaTiO 3 having an alkali metal oxide content of 0.04% by weight or less as an impurity, Tb 2 O 3 , Dy 2 O 3 , Ho
At least one rare earth oxide (Re 2 O 3 ) selected from 2 O 3 and Er 2 O 3 and Co 2 O 3 are the main components, and the compounding ratio is such that BaTiO 3 is 88.0 to 99.4 mol. %, Re 2 O 3 is 0.3 to 6.0 mol%, and Co 2 O 3 is 0.3 to 6.0 mol%. Based on 100 mol% of the main component, 0.2 to 4.0 mol% of BaO is added as an auxiliary component, and A non-reducing dielectric ceramic composition containing 0.2 to 3.0 mol% of MnO.
【請求項2】さらに、前記主成分100モル%に対して、
副成分として、Y2O3を3モル%以下含有する、特許請求
の範囲第1項記載の非還元性誘電体磁器組成物。
2. The method according to claim 1, further comprising:
2. The non-reducing dielectric ceramic composition according to claim 1, wherein the composition contains 3 mol% or less of Y 2 O 3 as an auxiliary component.
JP2311924A 1990-11-16 1990-11-16 Non-reducing dielectric porcelain composition Expired - Lifetime JP2920688B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2311924A JP2920688B2 (en) 1990-11-16 1990-11-16 Non-reducing dielectric porcelain composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2311924A JP2920688B2 (en) 1990-11-16 1990-11-16 Non-reducing dielectric porcelain composition

Publications (2)

Publication Number Publication Date
JPH04184809A JPH04184809A (en) 1992-07-01
JP2920688B2 true JP2920688B2 (en) 1999-07-19

Family

ID=18023068

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2311924A Expired - Lifetime JP2920688B2 (en) 1990-11-16 1990-11-16 Non-reducing dielectric porcelain composition

Country Status (1)

Country Link
JP (1) JP2920688B2 (en)

Also Published As

Publication number Publication date
JPH04184809A (en) 1992-07-01

Similar Documents

Publication Publication Date Title
JP3227859B2 (en) Non-reducing dielectric ceramic composition
JP4446324B2 (en) Dielectric porcelain composition and capacitor using the same
JP3028503B2 (en) Non-reducing dielectric porcelain composition
JPH04218207A (en) Dielectric porcelain composition
JP2958817B2 (en) Non-reducing dielectric porcelain composition
JP2004238251A (en) Dielectric ceramic composition and ceramic electronic component
JP2958819B2 (en) Non-reducing dielectric porcelain composition
JP2958818B2 (en) Non-reducing dielectric porcelain composition
JP2920693B2 (en) Non-reducing dielectric porcelain composition
JP2869900B2 (en) Non-reducing dielectric porcelain composition
JP2920688B2 (en) Non-reducing dielectric porcelain composition
JP3109171B2 (en) Non-reducing dielectric porcelain composition
JP3120500B2 (en) Non-reducing dielectric porcelain composition
JP2958820B2 (en) Non-reducing dielectric porcelain composition
JP2958822B2 (en) Non-reducing dielectric porcelain composition
JP2958823B2 (en) Non-reducing dielectric porcelain composition
JPH06227861A (en) Dielectric ceramic composition
JP3185333B2 (en) Non-reducing dielectric ceramic composition
JP2958824B2 (en) Non-reducing dielectric porcelain composition
JP3185331B2 (en) Non-reducing dielectric ceramic composition
JP3087387B2 (en) Non-reducing dielectric porcelain composition
JP3368599B2 (en) Non-reducing dielectric porcelain composition
JPH09255421A (en) High permittivity porcelain composition having slight dielectric loss
JP2958826B2 (en) Dielectric porcelain composition
JPH04368709A (en) Nonreducing dielectric porcelain composition material

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090430

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090430

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100430

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110430

Year of fee payment: 12

EXPY Cancellation because of completion of term
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110430

Year of fee payment: 12