JP3662158B2 - Method for producing slaked lime - Google Patents

Method for producing slaked lime Download PDF

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JP3662158B2
JP3662158B2 JP2000027662A JP2000027662A JP3662158B2 JP 3662158 B2 JP3662158 B2 JP 3662158B2 JP 2000027662 A JP2000027662 A JP 2000027662A JP 2000027662 A JP2000027662 A JP 2000027662A JP 3662158 B2 JP3662158 B2 JP 3662158B2
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Prior art keywords
slaked lime
water
lime
digestion
particles
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JP2001220185A (en
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チョ チョ
義夫 太田
哲志 岩下
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矢橋工業株式会社
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Description

【0001】
【発明の属する技術分野】
本発明は飲料水の水処理、廃水処理、排ガス処理、鋳物や製線用潤滑剤などの用途に有用な微粒子の消石灰を製造するための方法に関する。
【0002】
【従来の技術】
消石灰は水処理工程、有害ガスの除去、鋳物や製線用潤滑剤などとして、広く使用されている。これらの用途において、より小さい粒径の消石灰を用いればその効率や効果を高められることが知られている。例えば消石灰スラリーを用いた排ガスの脱硫工程においては、一般に、より微粒子の消石灰ほど浄化能力や効率が高くなる。よって、より微細な粒子からなる消石灰の製造方法が求められている。例えば消石灰スラリーを消化反応槽−ポンプ−インラインミキサー−サイクロン−消化反応槽と循環させながら、サイクロンよりメディアン径1μm以下の消石灰粒子からなる消石灰スラリーを得る方法がドイツ特許No.DE2714858に示されいる。しかしながらこの方法は、工程が複雑で長い時間を要する。
【0003】
【発明が解決しようとする課題】
よって本発明の目的は、例えば1μm以下の微粒子の消石灰粒子からなるスラリー状もしくはペースト状の消石灰を簡便に効率よく製造する方法を提供することにある。
【0004】
【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、以下の2つの工程を含む消石灰の製造方法を構成した。すなわち(a)工程:純度95重量%以上、活性度(t60)100秒以下、大きさ35mm以下の生石灰と、温度80〜95℃の水とを、1.2〜1.8の水比(水/生石灰(重量比))で、圧力下においてせん断及び/または混練しつつ混合して生石灰を消化する工程と、(b)工程:(a)工程で得られたペースト状消石灰にさらに水を加え、撹拌しつつ消化反応を実質的に完全にする工程である。さらに、(c)工程:(b)工程で得られた消石灰を所望の濃度の消石灰スラリーに調整し、粗粒子を取り除く工程を含むこともできる。
【0005】
消化工程において、消石灰の品質を左右する主な要因として、以下のようなものが挙げられる。
(1)生石灰の水との反応性
(2)生石灰の粒度分布
(3)使用する水の量と品質
(4)水温
(5)消化方式
(6)消化中の撹拌
【0006】
生石灰の水との反応性(活性度(t60))試験は、所定の大きさの生石灰150gを20℃の水600mLに加え、消化の進行中、カロリーメーターとストップウォッチを用いて、60℃に達するまでの時間を測定する。この試験はAWWA B202およびASTM C110で標準化されている。
【0007】
消化のメカニズムは、一般に、2〜3分の短い間に生石灰塊の表面にすばやく消化相が生成される段階と、消化による発熱を伴いながら生石灰塊が破裂するまでの10〜30分間に生石灰塊内部に徐々に消化相が生成される段階の二つの段階とに分けることができる。このメカニズムは、制御しにくく、均一な反応を生じさせるのは困難である。一般に、消化速度を速めるほど水酸化カルシウムの過飽和度が高まり、大量の核生成が生じ、最終的により微粒の消石灰を生成させることができることが知られている。従って消化速度が遅くなるのを妨ぐために、生石灰表面層に生成される消石灰層を取り除くメカニズムが必要と考えられる。このためには、従来の消化撹拌を単に強めるだけでは不十分で、生石灰粒子を効果的に磨砕するために特別な応力を加えるメカニズムが要求され、微細な消石灰粒子を生成するため、生石灰塊の表面にすばやく消化相が生成される間に、高い温度と強い磨砕を与えることが最も重要であることが確認された。このことは、発明者は上記のような理論または他の特定の理論に拘束されることを望むものではないが、結果として微細な消石灰粒子が生成される事実により信じられるものである。
【0008】
よって本発明では、水/生石灰(重量比)の値である水比が低い、すなわち高濃度の状態において生石灰粒子を強く練ることと、それによって得られるペーストの凝集を分散させ、かつ、消化反応を完全にするように撹拌することとで、従来よりも微細な粒子の割合の多い消石灰を得た。
【0009】
【発明の実施の形態】
本発明においては、生石灰を消化させるとその体積が2.5倍以上に増大し、狭い空間に置けば約5000t/m2 にも達する膨張力を生じる性質を利用して加圧することができる。初期の消化反応を押し出し機やニーダーなどの内容物を前進させながら練ることができる加圧式消化装置を用いて行なえば、密閉された圧力容器内でせん断及び/または混練しつつ生石灰と消化水とを混合して消化することになり、生石灰粒子を粉砕して微細化するための大きな圧力とせん断力及び/または混練力を常時得ることができる。押し出し混練装置等の内部の密閉された狭い場所で消化中に上昇する温度及び圧力を考慮すると、生石灰粒子は高温・高圧の下で消化されたと結論される。したがって、高純度・高活性生石灰と熱水を低い水比で消化させる工程において、初期に押し出し機やニーダーを用い、続いて撹拌機を用いる本発明の消化方法によれば、従来から行われている消化方法よりはるかに微粒子、例えば粒径1μm以下の消石灰が得られる。
【0010】
押し出し混練装置等は初期の消化における反応の場としての役割を果たす。消化装置内では生石灰と水は狭い空間に閉ざされ、強いせん断力及び/または混練力を受けて破砕されながら消化され、徐々に前進する。水比が低い、つまり、高濃度の状態での強力なせん断及び/または混練は生石灰粒子を磨砕し崩壊させ、初期の消化反応を促進する。生石灰粒子の表面層の消化相をすばやく取り除き、破砕して内部の未反応の部分を水に曝すことで均一な反応を生じさせる。
【0011】
初期の消化の後、得られた消石灰ペーストにはさらに水が加えられ、攪拌される。例えば高速撹拌装置を使用して消石灰ペーストと水を混合し、凝集を分散させつつ消化反応を実質的に完全なものとする。なお、この凝集を分散させるための攪拌により、消石灰粒子はさらに磨砕され得る。
【0012】
(a)工程では、高純度・高活性の生石灰を、低い水比で、圧力下において剪断及び/または混練しつつ消化する。高純度・高活性の生石灰は、純度95%以上、活性度t60が100秒以下であり、水比は1.2〜1.8である。水の温度は80〜95℃である。消化装置としては、加圧式のもの、例えば押し出し混練装置を用い、1〜2分間消化させる。
【0013】
(b)工程では、(a)工程で得られた消石灰ペーストにさらに水を加え、攪拌しつつ消化反応を実質的に完全にする。例えば、消石灰ペーストを高速撹拌装置内に入れて、10〜20分間、熱水中で分散させる。このときの水比は1.75〜12.0、水の温度は60℃以上が好ましい。このときの撹拌羽根の周速は2m/s以上が好ましい。
【0014】
(c)工程では(b)工程で得られた消石灰スラリーを所望の濃度に希釈し、粗粒子を除去する。粗粒子の除去にはボールミルのような粉砕・摩砕装置やふるいのような分級装置を用いることができる。
【0015】
【発明の効果】
本発明によれば、例えば粒径約1μm以下のような微粒子からなる消石灰スラリーもしくはペーストを簡便に効率よく製造することができる。この消石灰を水処理工程、有害ガスの除去、鋳物や製線用潤滑剤などに使用することにより、従来より高い効率や効果を得ることができる。
【0016】
【実施例】
以下、本発明に係る微粒子からなる消石灰の製造方法の実施例について説明する。
【0017】
(実施例)
生石灰(JIS工業石灰の生石灰特号、純度95%以上、粒度5−35mm、t60=30秒)200gを、温度85℃の水275g(水比1.375)により、押し出し混練装置(竹内製作所製、NES−KO−KNEADER)を用いて連続消化させた。消石灰ペーストの装置内滞留時間は約1.5分間とし、装置のロータリーブレードの回転数は80rpmとした。得られたペーストを高速攪拌装置(新東科学製、BL600)に移し、水比6.125となるように60℃の水950gで希釈し、周速2m/sで10分間撹拌した。続いて目開き150μmのふるいで粗粒子を取り除いた消石灰スラリーを試料No.1とした。目開き150μmのふるい上に残った粗粒子の割合は約5重量%であった。図1は試料No.1の走査電子顕微鏡による観察写真であり、得られた消石灰粒子が実質的に全て粒径1μm以下であることが示された。
【0018】
(比較例)
消化に伴う膨張による圧力を受けない常圧式であるオープンタイプのニーダー(丸東製作所製、C138A)を用いて消化した。初期の消化装置以外、実施例1と同じ手順を繰り返して試料No.2を得た。図2は試料No.2の走査電子顕微鏡による観察写真で、粒径1μm以上の大きな消石灰粒子が多数観察された。
【図面の簡単な説明】
【図1】図1は、本発明に係る消石灰の製造方法の一実施例により製造された消石灰の顕微鏡写真である。
【図2】図2は、従来の消石灰の製造方法により製造された消石灰の顕微鏡写真である。
[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a method for producing fine slaked lime useful for uses such as drinking water treatment, wastewater treatment, exhaust gas treatment, castings and wire-forming lubricants.
[0002]
[Prior art]
Slaked lime is widely used as a water treatment process, removal of harmful gases, castings and wire-forming lubricants, and the like. In these applications, it is known that the efficiency and effect can be enhanced by using slaked lime having a smaller particle diameter. For example, in the exhaust gas desulfurization process using slaked lime slurry, generally, purification capacity and efficiency become higher as finer slaked lime. Therefore, a method for producing slaked lime composed of finer particles is required. For example, German Patent No. DE2714858 discloses a method for obtaining a slaked lime slurry composed of slaked lime particles having a median diameter of 1 μm or less from a cyclone while circulating the slaked lime slurry through a digestion reaction tank-pump-in-line mixer-cyclone-digestion reaction tank. However, this method has a complicated process and requires a long time.
[0003]
[Problems to be solved by the invention]
Accordingly, an object of the present invention is to provide a method for easily and efficiently producing slurry-like or paste-like slaked lime composed of fine slaked lime particles of, for example, 1 μm or less.
[0004]
[Means for Solving the Problems]
In order to achieve the above object, the present invention configures a method for producing slaked lime including the following two steps. That is, step (a): a quick lime having a purity of 95% by weight or more, an activity (t60) of 100 seconds or less, and a size of 35 mm or less, and water having a temperature of 80 to 95 ° C. and a water ratio of 1.2 to 1.8 ( Water / quick lime (weight ratio)), shearing and / or kneading under pressure and mixing to digest quick lime; and step (b): water is further added to the paste-like slaked lime obtained in step (a). In addition, it is a step of making the digestion reaction substantially complete while stirring. Furthermore, (c) process: The process of adjusting the slaked lime obtained at the (b) process to the slaked lime slurry of a desired density | concentration, and removing a coarse particle can also be included.
[0005]
The main factors that influence the quality of slaked lime in the digestion process include the following.
(1) Reactivity of quicklime with water (2) Particle size distribution of quicklime (3) Quantity and quality of water used (4) Water temperature (5) Digestion method (6) Agitation during digestion
The reactivity of quicklime with water (activity (t60)) test was performed by adding 150 g of quicklime of a predetermined size to 600 mL of water at 20 ° C, and using a calorimeter and a stopwatch at 60 ° C during the digestion. Measure the time to reach. This test has been standardized with AWWA B202 and ASTM C110.
[0007]
Generally, the digestion mechanism consists of a stage in which a digestive phase is quickly generated on the surface of the quicklime mass in a short period of 2 to 3 minutes, and a quicklime mass in 10 to 30 minutes until the quicklime mass bursts with heat generated by digestion. It can be divided into two stages in which a digestive phase is gradually generated inside. This mechanism is difficult to control and it is difficult to produce a uniform reaction. In general, it is known that as the digestion rate increases, the supersaturation degree of calcium hydroxide increases, a large amount of nucleation occurs, and finally finer slaked lime can be generated. Therefore, in order to prevent the digestion rate from becoming slow, a mechanism for removing the slaked lime layer formed on the quicklime surface layer is considered necessary. For this purpose, it is not sufficient to simply increase the conventional digestive agitation. A mechanism for applying special stress to effectively grind the quicklime particles is required, and fine slaked lime particles are produced. It was confirmed that it was most important to give high temperature and strong grinding during the rapid digestion phase formation on the surface of This is not believed by the inventor to be bound by the above theory or any other specific theory, but is believed by the fact that fine slaked lime particles are produced as a result.
[0008]
Therefore, in the present invention, the water ratio, which is the value of water / quick lime (weight ratio), is low, that is, the kneaded lime particles are strongly kneaded in a high concentration state, the agglomeration of the paste obtained thereby is dispersed, and By stirring so as to complete the slaked lime, the proportion of fine particles was higher than in the past.
[0009]
DETAILED DESCRIPTION OF THE INVENTION
In the present invention, when quicklime is digested, its volume increases 2.5 times or more, and if it is placed in a narrow space, it can be pressurized by utilizing the property of generating an expansion force reaching about 5000 t / m 2 . If the initial digestion reaction is carried out using a pressurized digester that can knead while advancing the contents of an extruder, kneader, etc., quick lime and digested water can be used while being sheared and / or kneaded in a sealed pressure vessel. Thus, a large pressure and shearing force and / or kneading force for pulverizing and refining the quicklime particles can be constantly obtained. Considering the temperature and pressure rising during digestion in an enclosed narrow space such as in an extrusion kneader, it is concluded that the quicklime particles were digested under high temperature and pressure. Therefore, in the step of digesting high purity and high activity quicklime and hot water at a low water ratio, according to the digestion method of the present invention using an extruder or a kneader at an initial stage and then using a stirrer, it has been conventionally performed. Fine particles, for example, slaked lime having a particle size of 1 μm or less, are obtained much more than conventional digestion methods.
[0010]
An extrusion kneader or the like serves as a reaction field in the initial digestion. In the digester, quick lime and water are confined in a narrow space, digested while being crushed under a strong shearing force and / or kneading force, and gradually move forward. Strong shearing and / or kneading at a low water ratio, i.e. high concentration, grinds and breaks up the quicklime particles and promotes the initial digestion reaction. The digestive phase of the surface layer of quicklime particles is quickly removed, crushed, and the unreacted portion inside is exposed to water to cause a uniform reaction.
[0011]
After the initial digestion, more water is added to the resulting slaked lime paste and stirred. For example, the slaked lime paste and water are mixed using a high-speed agitator to make the digestion reaction substantially complete while dispersing the agglomerates. The slaked lime particles can be further ground by stirring to disperse the agglomeration.
[0012]
In the step (a), high purity and highly active quicklime is digested at a low water ratio while being sheared and / or kneaded under pressure. High purity and high activity quicklime has a purity of 95% or more, an activity t60 of 100 seconds or less, and a water ratio of 1.2 to 1.8. The temperature of water is 80-95 ° C. As a digester, a pressure type device such as an extrusion kneader is used for digestion for 1 to 2 minutes.
[0013]
In the step (b), water is further added to the slaked lime paste obtained in the step (a), and the digestion reaction is substantially completed while stirring. For example, slaked lime paste is put in a high-speed stirring device and dispersed in hot water for 10 to 20 minutes. At this time, the water ratio is preferably 1.75 to 12.0, and the water temperature is preferably 60 ° C. or higher. At this time, the peripheral speed of the stirring blade is preferably 2 m / s or more.
[0014]
In step (c), the slaked lime slurry obtained in step (b) is diluted to a desired concentration to remove coarse particles. For removing the coarse particles, a pulverizing / milling device such as a ball mill or a classification device such as a sieve can be used.
[0015]
【The invention's effect】
According to the present invention, for example, a slaked lime slurry or paste made of fine particles having a particle size of about 1 μm or less can be easily and efficiently produced. By using this slaked lime in a water treatment process, removal of harmful gases, castings, wire-forming lubricants, and the like, higher efficiency and effects than before can be obtained.
[0016]
【Example】
Hereinafter, the Example of the manufacturing method of the slaked lime which consists of microparticles | fine-particles based on this invention is described.
[0017]
(Example)
Quick lime (special lime of JIS industrial lime, purity 95% or more, particle size 5-35 mm, t60 = 30 seconds) 200 g is extruded and kneaded with water 275 g (water ratio 1.375) at a temperature of 85 ° C. (manufactured by Takeuchi Seisakusho). , NES-KO-KNEADER). The residence time of the slaked lime paste in the apparatus was about 1.5 minutes, and the rotation speed of the rotary blade of the apparatus was 80 rpm. The obtained paste was transferred to a high-speed stirrer (manufactured by Shinto Kagaku, BL600), diluted with 950 g of water at 60 ° C. to a water ratio of 6.125, and stirred at a peripheral speed of 2 m / s for 10 minutes. Subsequently, slaked lime slurry from which coarse particles were removed with a sieve having an opening of 150 μm was used as a sample No. It was set to 1. The proportion of coarse particles remaining on the sieve having an opening of 150 μm was about 5% by weight. FIG. 1 is an observation photograph by a scanning electron microscope, and it was shown that the obtained slaked lime particles were substantially all having a particle size of 1 μm or less.
[0018]
(Comparative example)
Digestion was performed using an open-type kneader (manufactured by Maruto Seisakusho, C138A) that does not receive pressure due to expansion due to digestion. Except for the initial digester, the same procedure as in Example 1 was repeated to obtain the sample No. 2 was obtained. FIG. A large number of large slaked lime particles having a particle diameter of 1 μm or more were observed in the observation photograph taken by scanning electron microscope 2.
[Brief description of the drawings]
FIG. 1 is a photomicrograph of slaked lime produced by an example of a method for producing slaked lime according to the present invention.
FIG. 2 is a photomicrograph of slaked lime produced by a conventional method for producing slaked lime.

Claims (2)

以下の2つの工程を含んで構成されることを特徴とする消石灰の製造方法。
(a)工程:純度95重量%以上、活性度(t60)100秒以下、大きさ35mm以下の生石灰と、温度80〜95℃の水とを、1.2〜1.8の水比(水/生石灰(重量比))で、圧力下においてせん断及び/または混練しつつ混合して生石灰を消化する工程。
(b)工程:(a)工程で得られたペースト状消石灰にさらに水を加え、撹拌しつつ消化反応を実質的に完全にする工程。
The manufacturing method of the slaked lime characterized by including the following two processes.
(A) Step: A quick lime having a purity of 95% by weight or more, an activity (t60) of 100 seconds or less, and a size of 35 mm or less, and water having a temperature of 80 to 95 ° C. and a water ratio of 1.2 to 1.8 (water / Quick lime (weight ratio)) and digesting quick lime by mixing while shearing and / or kneading under pressure.
(B) Step: A step of further adding water to the paste-like slaked lime obtained in the step (a) to substantially complete the digestion reaction while stirring.
さらに、(c)工程:(b)工程で得られた消石灰を所望の濃度の消石灰スラリーに調整し、粗粒子を取り除く工程を含む請求項1に記載の消石灰の製造方法。Furthermore, the manufacturing method of the slaked lime of Claim 1 including the process of adjusting the slaked lime obtained at the (c) process: (b) process to the slaked lime slurry of a desired density | concentration, and removing a coarse particle.
JP2000027662A 2000-02-04 2000-02-04 Method for producing slaked lime Expired - Fee Related JP3662158B2 (en)

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JP4513277B2 (en) * 2003-05-23 2010-07-28 東レ株式会社 Method for producing slaked lime slurry
JP4799470B2 (en) * 2007-04-17 2011-10-26 奥多摩工業株式会社 Method for producing slaked lime slurry
KR100880128B1 (en) 2008-07-24 2009-01-23 주식회사 서울아이씨 Method for making lime slurry with high-speed agitation
JP5600386B2 (en) * 2008-11-05 2014-10-01 奥多摩工業株式会社 Method for producing plate-like calcium hydroxide
BE1021522B1 (en) 2012-09-12 2015-12-07 S.A. Lhoist Recherche Et Developpement HIGH FINENSE LIME MILK COMPOSITION
JP2016008148A (en) * 2014-06-23 2016-01-18 株式会社トクヤマ METHOD FOR PRODUCING Ca(OH)2 AQUEOUS SLURRY
CN111116061A (en) * 2019-12-31 2020-05-08 米易东立矿业有限公司 Dry preparation method of nano calcium hydroxide

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