JP2009001826A - Gasification method of biomass - Google Patents

Gasification method of biomass Download PDF

Info

Publication number
JP2009001826A
JP2009001826A JP2008225517A JP2008225517A JP2009001826A JP 2009001826 A JP2009001826 A JP 2009001826A JP 2008225517 A JP2008225517 A JP 2008225517A JP 2008225517 A JP2008225517 A JP 2008225517A JP 2009001826 A JP2009001826 A JP 2009001826A
Authority
JP
Japan
Prior art keywords
biomass
gasification
space
reaction
external heating
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
JP2008225517A
Other languages
Japanese (ja)
Other versions
JP4665021B2 (en
Inventor
Kimiyo Tokuda
君代 徳田
Toshimitsu Ichinose
利光 一ノ瀬
Yoshinori Kobayashi
由則 小林
Masayasu Sakai
正康 坂井
Nobuaki Murakami
信明 村上
Toshiyuki Takegawa
敏之 竹川
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.)
Mitsubishi Heavy Industries Ltd
Nagasaki Institute of Applied Science
Original Assignee
Mitsubishi Heavy Industries Ltd
Nagasaki Institute of Applied Science
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 Mitsubishi Heavy Industries Ltd, Nagasaki Institute of Applied Science filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP2008225517A priority Critical patent/JP4665021B2/en
Publication of JP2009001826A publication Critical patent/JP2009001826A/en
Application granted granted Critical
Publication of JP4665021B2 publication Critical patent/JP4665021B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Landscapes

  • Processing Of Solid Wastes (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a gasification method of biomass, which is possible even in a small scale, for obtaining a highly calorific clean fuel gas suited for a power generation gas engine in a high yield from biomass resources. <P>SOLUTION: The gasification method of biomass comprises as follows. A biomass fine powder which consists of grass plants or woody plants is supplied into a gasification space intercepted by an external heating space and a dividing wall. Heating is performed through the dividing wall from the external heating space, thereby the gasification reaction between a high temperature steam blown into the gasification space and biomass is generated in the gasification space by an endothermic reaction. In addition, in the molecular formula of CmH<SB>2</SB>On of the biomass, when m is 1.3 and n is 0.9, the molar ratio of the water vapor/biomass is established as 0.3-15. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明はバイオマスの有効利用に関し、詳しくは、バイオマスからクリーンな高カロリガスを生成させる方法に関する。更には、従来のバイオマスエネルギ利用形態では得られないシステム発電効率の高い、給電システムもしくは熱電併給システムのガスエンジンに使用可能な、クリーンな高カロリガスの生成方法に関する。   The present invention relates to effective use of biomass, and more particularly to a method for producing clean high calorie gas from biomass. Furthermore, the present invention relates to a method for producing clean, high calorie gas that can be used for a gas engine of a power supply system or a combined heat and power system with high system power generation efficiency that cannot be obtained by a conventional form of biomass energy utilization.

従来のバイオマスエネルギ利用形態のうち、電気エネルギもしくは熱電両エネルギに変換して行う利用形態では、バイオマスをボイラ用燃料として直接燃焼して、高圧蒸気を生成させ、発電用タービンを回転させる方式が執られている。従って、少なくとも5000〜10000kWと設備規模が大きくなるので、バイオマス資源の大量集約的発生もしくは大量収集が必要である。加えて、多額な投下資本を必要とする。なによりも、その発電効率が5000kW規模の場合で10%台に留まっているため、小規模で効率の高いバイオマス資源の利用形態が望まれている。   Among conventional biomass energy utilization forms, the utilization form performed by converting into electric energy or thermoelectric energy directly burns biomass as boiler fuel, generates high-pressure steam, and rotates the power generation turbine. It has been. Therefore, since the scale of the facility is increased to at least 5000 to 10,000 kW, it is necessary to generate a large amount of biomass resources or to collect a large amount of biomass resources. In addition, it requires a large amount of invested capital. Above all, since the power generation efficiency is in the range of 10% in the case of the 5000 kW scale, a small and highly efficient use form of biomass resources is desired.

一方、ガスエンジン使用の発電では小規模でも高い発電効率が得られるので、我が国のようにバイオマス資源が分散的に発生する社会および自然環境ではバイオマスのガス化技術の必要性が高い。   On the other hand, since power generation using a gas engine can achieve high power generation efficiency even on a small scale, there is a high need for biomass gasification technology in a society and natural environment where biomass resources are generated in a distributed manner as in Japan.

バイオマスのガス化技術については、従来より固定床、流動床型のガス化炉で、酸素もしくは空気を主たるガス化剤として、吸熱反応であるガス化の空間と燃焼による発熱空間を共通の空間に設定した、いわゆる内燃式のものが研究開発されてきたが、タール、煤が副生し、ガスエンジン用として品質が適合しない。加えて、空気を用いる場合には、生成ガス中に窒素が残留して、単位生成ガスの発熱量を低下させる。酸素を用いる場合には、空気分離工程が別に必要で、運転に要するエネルギ及び設備投資がエネルギ効率低下要因及びコストプッシュ要因となる。   With regard to biomass gasification technology, in a conventional fixed bed and fluidized bed type gasification furnace, oxygen or air is the main gasifying agent, and gasification space, which is an endothermic reaction, and heat generation space due to combustion are made into a common space. The so-called internal combustion type that has been set has been researched and developed, but tar and soot are by-produced and the quality is not suitable for gas engines. In addition, when air is used, nitrogen remains in the product gas, and the calorific value of the unit product gas is reduced. In the case of using oxygen, an air separation step is separately required, and energy required for operation and capital investment are factors for lowering energy efficiency and cost push.

他に、臨界圧熱水によるガス化研究が行われているが、超高温高圧操作上の問題を含み、実用化の域に達していない。   In addition, gasification research using critical-pressure hot water has been conducted, but it has not reached the range of practical use due to problems with ultra-high temperature and high-pressure operation.

本発明はかかる従来の問題点に鑑みてなされたもので、バイオマス資源から発電用ガスエンジンに適合する、高カロリで、クリーンな燃料ガスを、高収率で取得する、小規模でも可能なバイオマスのガス化方法を提供することを目的とする。加えて、バイオマス資源の総合的エネルギ転換効率を高め、第三の新エネルギとしての利用普及に寄与せんとするものである。   The present invention has been made in view of such conventional problems, and is capable of obtaining high-calorie, clean fuel gas in high yield, which is suitable for a power generation gas engine from biomass resources, and can be produced even on a small scale. It aims at providing the gasification method of this. In addition, it will increase the overall energy conversion efficiency of biomass resources and contribute to the spread of use as a third new energy.

本発明のバイオマスのガス化方法は、粉砕した草本類若しくは木本類からなるバイオマス微粉を、外部加熱空間と隔壁により遮断されたガス化空間内に供給して、且つ前記外部加熱空間より隔壁を介して加熱して、吸熱反応によりガス化空間内で、該ガス化空間内に吹き込まれる高温水蒸気とバイオマスのガス化反応を生じせしめるバイオマスのガス化方法であって、前記バイオマスの分子式CmHOnにおいて、m=1.3、n=0.9とした場合の、前記水蒸気/バイオマスのモル比を0.3〜15に設定したことを特微とする。 The biomass gasification method of the present invention supplies biomass fine powder made of pulverized herbs or trees into a gasification space blocked by an external heating space and a partition wall, and the partition wall is formed from the external heating space. A gasification method of biomass that causes a gasification reaction of high-temperature steam and biomass that is blown into the gasification space by an endothermic reaction, the molecular formula CmH 2 On of the biomass The feature is that the molar ratio of water vapor / biomass is set to 0.3 to 15 when m = 1.3 and n = 0.9.

バイオマスの分解に必要な熱を、ガス化空間には化学的に影響を及ぼさない反応管壁からの輻射により、別途用意した熱源で供給することに加えて、バイオマス即ちCmHOnに対する水蒸気即ちHOをモル比(水蒸気/バイオマス)で0.3〜15の範囲で反応させることが、遊離炭素のない、即ちタール・煤のない組成で、エネルギ密度の高いガスを生成させることにおいて必須である。好ましくは、この水蒸気/バイオマスモル比は0.35〜5がよい。またガス化空間で酸素による酸化反応が進行するときは、ミクロ的にみた局部で、極端な過熱現象も発生し得るので、遊離炭素の生成など好ましくない副反応が起こる。よって、隔壁を介した間接加熱が好ましい。実質的には酸素濃度を2%以下であるするのが好ましい。 In addition to supplying the heat necessary for the decomposition of the biomass with a separately prepared heat source by radiation from the reaction tube wall that does not chemically affect the gasification space, the steam for the biomass, that is, CmH 2 On, that is, H It is indispensable to react 2 O in a molar ratio (water vapor / biomass) in the range of 0.3 to 15 in order to produce a gas having a high energy density with no free carbon, that is, a composition free of tar and soot. is there. Preferably, the water vapor / biomass molar ratio is 0.35-5. Further, when the oxidation reaction with oxygen proceeds in the gasification space, an extreme overheating phenomenon may occur locally in a microscopic view, and thus undesirable side reactions such as the formation of free carbon occur. Therefore, indirect heating through a partition is preferable. It is preferable that the oxygen concentration is substantially 2% or less.

バイオマスの分子式CmHOnにおいて、通常得られる草本類、木質類では平均的にm=1.3、n=0.9と考えて前記モル比を設定してよい。別途用意する熱源はバイオマスを燃焼して得られる熱ガスを用いることができる。この熱源用バイオマスはガス分解用の原料より低品位のバイオマスを使用することもできる。 In the molecular formula CmH 2 On of biomass, the above-mentioned molar ratio may be set assuming that m = 1.3 and n = 0.9 on average in herbs and woods that are usually obtained. As a separately prepared heat source, a hot gas obtained by burning biomass can be used. As the heat source biomass, biomass having a lower quality than the raw material for gas decomposition can be used.

更に本発明のバイオマスのガス化方法は、外部から加える熱量が25Kcal/バイオマスモル以上、好ましくは30Kcal/バイオマスモル以上、更に好ましくは39.7Kcal/バイオマスモル以上であることを特徴とする。   Furthermore, the biomass gasification method of the present invention is characterized in that the amount of heat applied from the outside is 25 Kcal / biomass mole or more, preferably 30 Kcal / biomass mole or more, more preferably 39.7 Kcal / biomass mole or more.

本発明の目的とするクリーンで高カロリなガスを生成させる吸熱反応では、化学量論的には39.7Kcal/バイオマスモルであるので、速やかに副反応を伴わずに、反応を進行させるには少なくとも25Kcal/バイオマスモルの熱量が必要となる。そして、ガス化装置のガス化反応領域内での滞留時間はおよそ0.1〜10秒の範囲を要し、反応領域内の温度がおよそ850〜1000℃の範囲では0.1秒、およそ800℃では0.2〜0.5秒、およそ750℃では10秒の滞留時間とすることが好ましい。   In the endothermic reaction that produces a clean, high caloric gas, which is the object of the present invention, the stoichiometric amount is 39.7 Kcal / biomass mole, so that the reaction can proceed rapidly without side reactions. A calorific value of at least 25 Kcal / biomass mole is required. The residence time in the gasification reaction zone of the gasifier requires a range of about 0.1 to 10 seconds, and when the temperature in the reaction zone is about 850 to 1000 ° C., the residence time is 0.1 seconds and about 800. It is preferable that the residence time is 0.2 to 0.5 seconds at C, and 10 seconds at about 750C.

更に本発明のバイオマスのガス化方法は、外部より隔壁を介してガス化空間内の前記バイオマスに加える熱量がガス化反応後にすす若しくはタールが生じないようにガス化空間内の水蒸気の熱量及び隔壁からの外部熱量を調整して供給することを特微とする。   Furthermore, the biomass gasification method according to the present invention includes the heat amount of water vapor in the gasification space and the partition wall so that the amount of heat applied to the biomass in the gasification space from outside through the partition wall does not generate soot or tar after the gasification reaction. The feature is to adjust the amount of external heat from the supply.

ガス化空間における分解ガス生成反応においては勿論のこと、生成したガス中のハイドロカーボンが脱水素して、遊離の炭素を生成しない条件とすることも必要であって、水蒸気量と温度即ち外部供給熱量を適切に調節して行う必要がある。   In addition to the cracking gas generation reaction in the gasification space, it is also necessary that the hydrocarbon in the generated gas is dehydrogenated and free carbon is not generated. It is necessary to adjust the amount of heat appropriately.

更に本発明のバイオマスのガス化方法は、下記(1)式の条件を満たすように、前記水蒸気/バイオマスのモル比と外部加熱空間よりの外部加熱カロリ及びガス化空間の還元雰囲気を設定したことを特微とする。
1.30.9+p
→q+qCO+qCH+qCO …(1)
前記(1)式の一例を以下に示す。
1.30.9+0.4H
→0.8H+0.7CO+0.3CH+0.3CO
Further, in the biomass gasification method of the present invention, the water vapor / biomass molar ratio, the external heating calorie from the external heating space, and the reducing atmosphere of the gasification space are set so as to satisfy the following formula (1). Is a feature.
C 1.3 H 2 O 0.9 + p 1 H 2 O
→ q 1 H 2 + q 2 CO + q 3 CH 4 + q 4 CO 2 (1)
An example of the formula (1) is shown below.
C 1.3 H 2 O 0.9 +0.4 H 2 O
→ 0.8H 2 + 0.7CO + 0.3CH 4 + 0.3CO 2

即ち、(1)式は本発明の目的とする反応式であり、水蒸気/バイオマスのモル比と外部加熱カロリ及びガス化空間の還元雰囲気(酸素不足雰囲気)を設定することにより可能な反応式であることを見出した。   In other words, the equation (1) is a reaction equation aimed at by the present invention, and is a reaction equation that is possible by setting the steam / biomass molar ratio, the externally heated calories and the reducing atmosphere (oxygen-deficient atmosphere) of the gasification space. I found out.

更に本発明のバイオマスのガス化方法は、炉内ガス化温度が800〜1000℃で、且つガス化雰囲気が常圧下で触媒を用いない還元性雰囲気であることを特徴とする。ガス化の温度範囲は副反応を伴わず且つ迅速に前記目的反応を促進的に進行させるのに足る温度範囲として前記範囲が好ましく、特に圧力を高める必要がない。そして、温度は微粉体がガスに転換する速度に関係があり、850〜950℃では最長凡そ0.2秒の転換速度が必要で、800℃〜850では最長凡そ0.5秒の転換速度が必要である。更に1000℃付近を超えると、装置の材質に非常に高価な耐熱性のものを選択する必要が生じるなど不利となる。還元性雰囲気とは酸化剤の存在しない雰囲気も含み、これにより、酸化熱による局部的な高温による副反応を伴わない専ら分解反応によるガス化が進行する。この種の炭水素酸素化合物の水蒸気による分解では、例えばニッケル系の触媒の存在下で、促進される場合があるが、本発明の方法では、特に触媒の必要はなく本発明の限定する条件で行えば、実用的な速度で進行する。通常、バイオマス有機物であるため、蛋白質や不純物由来の硫黄分及び塩素分が若干混入するので、これにより触媒は被毒され、実際には効果がない。   Furthermore, the biomass gasification method of the present invention is characterized in that the in-furnace gasification temperature is 800 to 1000 ° C., and the gasification atmosphere is a reducing atmosphere using no catalyst under normal pressure. The temperature range for gasification is preferably a temperature range that is not accompanied by side reactions and is sufficient to rapidly promote the target reaction, and it is not particularly necessary to increase the pressure. The temperature is related to the speed at which the fine powder is converted into gas. A conversion speed of up to about 0.2 seconds is required at 850 to 950 ° C., and a conversion speed of up to about 0.5 seconds is required at 800 to 850 ° C. is necessary. Further, when the temperature exceeds about 1000 ° C., it is disadvantageous that it is necessary to select a very expensive heat-resistant material for the device. The reducing atmosphere also includes an atmosphere in which no oxidant is present, whereby gasification proceeds exclusively through a decomposition reaction without a side reaction due to a local high temperature due to oxidation heat. The decomposition of this type of hydrocarbon-oxygen compound with water vapor may be promoted, for example, in the presence of a nickel-based catalyst. However, in the method of the present invention, there is no need for a catalyst and the conditions limited by the present invention are used. If done, it will proceed at a practical rate. Usually, since it is a biomass organic substance, sulfur and chlorine derived from proteins and impurities are slightly mixed in, so that the catalyst is poisoned and has no effect in practice.

更に本発明のバイオマスのガス化方法は、粉砕した草本類若しくは木本類からなるバイオマスに、水蒸気を供給してガス化反応を生じせしめるガス化空間が、隔壁を構成する金属反応管を介して外部加熱空間と遮断され、前記金属反応管の管壁を介してガス化空間に幅射熱が付与されるようにしたことを特微とする。本反応ではできる限り純粋に目的反応を進行させ、有害な副反応を排除するために、加熱源たる熱ガスを直接ガス化空間に導入しない。熱のみをガス化空間に導入できる手段である、隔壁に熱ガスより伝熱し、その温度による隔壁のガス化空間内部への輻射による加熱手段を用いる。また、この方法により、熱ガスの化学的純度に多少の問題があってもガス化反応には影響しないから、加熱源としてのみの役割を果たしうる。なお、生成ガス中の若干の硫黄分及び塩素分は後述するとおり、生成ガス中の水分除去とともに、後段の脱水工程で除去可能である。   Furthermore, in the method for gasifying biomass according to the present invention, the gasification space in which the gasification reaction is caused by supplying water vapor to the biomass consisting of pulverized herbs or woods via the metal reaction tube constituting the partition wall. It is characterized in that it is cut off from the external heating space, and width radiation heat is applied to the gasification space through the tube wall of the metal reaction tube. In this reaction, in order to advance the target reaction as purely as possible and eliminate harmful side reactions, a hot gas as a heating source is not directly introduced into the gasification space. Heating means that transfers heat from the hot gas to the partition walls, which is a means that can introduce only heat into the gasification space, and uses radiation to radiate the partition walls into the gasification space depending on the temperature. Further, by this method, even if there is some problem in the chemical purity of the hot gas, it does not affect the gasification reaction, so it can serve only as a heating source. Note that, as will be described later, some sulfur and chlorine in the product gas can be removed in the subsequent dehydration step together with the removal of moisture in the product gas.

以上本発明の特徴により、タール、煤など遊離炭素の発生を伴わない、廃棄物は若干の灰分のみの、クリーンなH、CO、及びCHなどの炭化水素を主成分とする浮遊・外熱式高カロリガス(例えば20MJ/NM)が得られ、ガスエンジン発電と組合すことにより、総合エネルギ効率の高いシステムとすることができる。 As described above, according to the features of the present invention, there is no generation of free carbon such as tar and soot, and the waste is only a small amount of ash, and is mainly floating or outside mainly composed of hydrocarbons such as clean H 2 , CO, and CH 4. Thermal high calorie gas (for example, 20 MJ / NM 3 ) can be obtained, and a system with high total energy efficiency can be obtained by combining with gas engine power generation.

以下に本発明の実施の形態について図面を参照して詳しく説明する。但し本実施の形態に記載される製品の寸法、形状、材質、その相対配置等は特に特定的な記載がない限りは本発明の範囲をそれのみに限定する主旨ではなく、単なる説明例に過ぎない。   Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. However, the dimensions, shapes, materials, relative arrangements, etc. of the products described in the present embodiment are not intended to limit the scope of the present invention only to specific examples unless otherwise specified, but are merely illustrative examples. Absent.

(実施例1) 図1は本発明の浮遊・外熱式高カロリガスを生成するガス化反応設備を中心とするバイオエネルギ利用システムのフロー図である。ガス化反応設備101は反応管306(図2、3参照)を備え、該反応管は反応水115及びバイオマス微粉112を受け入れ、外部からバイオマス燃焼高温ガス114により加熱できるよう構成されている。粉砕設備102はバイオマスを受け入れて平均粒径3mm以下、好ましくは1mm以下の微粉を生成可能な性能を有し、平均粒径3mm以下の微粉112と平均粒径3mmを超える粗粉113を分別して、排出可能な構造を有している。本実施例では破砕機とインパクトミルを組み合わせて用いた。熱ガス発生炉103はバイオマス粗粉113を受け入れて空気などの支燃剤によりバイオマス粗粉113を燃焼して高温のバイオマス燃焼高温ガス114を生成する。脱水装置104は内部に冷却伝熱面を持ち、塔内に導入されたガス中の水分及び硫黄化合物など高沸点物を凝縮して除去可能な構造を有す。ガスタンク105は水封式のタンクで、生成ガスを貯留可能な構造になっている。ガスエンジン106は本例における生成ガスを燃焼して、発電機を運転可能な能力を有している。 (Example 1) FIG. 1 is a flow chart of a bioenergy utilization system centering on a gasification reaction facility for generating floating / externally heated high calorie gas of the present invention. The gasification reaction equipment 101 includes a reaction tube 306 (see FIGS. 2 and 3), and the reaction tube is configured to receive the reaction water 115 and the biomass fine powder 112 and to be heated by the biomass combustion hot gas 114 from the outside. The pulverization facility 102 has a performance capable of receiving biomass and generating fine powder having an average particle diameter of 3 mm or less, preferably 1 mm or less, and separating fine powder 112 having an average particle diameter of 3 mm or less and coarse powder 113 having an average particle diameter of 3 mm or more. It has a structure that can be discharged. In this example, a crusher and an impact mill were used in combination. The hot gas generation furnace 103 receives the biomass coarse powder 113 and burns the biomass coarse powder 113 with a combustion support agent such as air to generate a high-temperature biomass combustion hot gas 114. The dehydrator 104 has a cooling heat transfer surface inside, and has a structure capable of condensing and removing high-boiling substances such as moisture and sulfur compounds in the gas introduced into the tower. The gas tank 105 is a water-sealed tank and has a structure capable of storing generated gas. The gas engine 106 has the capability of burning the generated gas in this example and operating the generator.

図1において、バイオマス原料111は粉砕設備102に供給され平均粒径3mm以下の微粉112と平均粒径3mmを超える粗粉113に分けられ、粗粉113は熱ガス発生炉103に送られ、微粉112はガス化反応設備101中の前記反応管306中に反応水115とともに導入される。熱ガス発生炉103では粗粉113を燃焼温度900〜1200℃で燃焼させ、発生するバイオマス燃焼高温ガス114でガス化反応設備101中の前記反応管306を外部から加熱し、管内の温度を800℃以上に保つ。反応管内に導入された微粉112は導入反応水115によって発生した水蒸気気流中に浮遊し、ほぼ瞬時(0.2秒以下)にガス化する。生成ガス118を脱水装置104に導入し、水分と硫黄分(HS)、塩素分(HCl)を除去した後、生成ガス116とし、ガスタンク105に貯留する。生成ガス116は約20MJ/mのカロリを有し、ガスエンジン106用燃料として適合する。本システムでバイオマス処理量1トン/日(50〜100kg/h)を処理して、30kWの発電機により電気エネルギに変換したときの、総合エネルギ効率は20%以上とすることができた。 In FIG. 1, the biomass raw material 111 is supplied to the pulverization facility 102 and is divided into fine powder 112 having an average particle diameter of 3 mm or less and coarse powder 113 having an average particle diameter of 3 mm, and the coarse powder 113 is sent to the hot gas generation furnace 103 to be fine powder. 112 is introduced together with the reaction water 115 into the reaction tube 306 in the gasification reaction facility 101. In the hot gas generation furnace 103, the coarse powder 113 is burned at a combustion temperature of 900 to 1200 ° C., and the reaction tube 306 in the gasification reaction facility 101 is heated from the outside with the generated biomass combustion hot gas 114, and the temperature in the tube is set to 800. Keep above ℃. The fine powder 112 introduced into the reaction tube floats in the water vapor stream generated by the introduced reaction water 115 and is gasified almost instantaneously (0.2 seconds or less). The product gas 118 is introduced into the dehydrator 104 to remove moisture, sulfur content (H 2 S), and chlorine content (HCl), and the product gas 116 is stored in the gas tank 105. The product gas 116 has a calorie of about 20 MJ / m 3 and is suitable as a fuel for the gas engine 106. The total energy efficiency when a biomass throughput of 1 ton / day (50 to 100 kg / h) was processed by this system and converted into electric energy by a 30 kW generator could be 20% or more.

(実施例2) 図2は本発明のガス化反応設備101と1次ガス化部302詳細の一例の概要図である。図2において、ガス化反応設備101は、加熱チャンバ307内部に反応管306を有し、加熱チャンバ307はバイオマス燃焼高温ガス114の導入口と、排出口を備えている。反応管はU字、逆U字、U字の管を連結した曲管であり、右側より第一垂直部、第二垂直部、第三垂直部、第四垂直部がある。その右端の第一垂直部上部より反応水115を導入出来る開口端が、中途第二垂直部上部よりバイオマス微粉112が導入出来る開口端が、中途第二垂直部、第三垂直部とを連結するU字管底部よりガス化によって発生する灰117を取り出す開口端が、左端第四垂直部よりガス化反応で生成した含水生成ガス118を取り出す開口端が、夫々設けてある。 (Example 2) FIG. 2: is a schematic diagram of an example of the details of the gasification reaction equipment 101 and the primary gasification part 302 of this invention. In FIG. 2, the gasification reaction equipment 101 has a reaction tube 306 inside a heating chamber 307, and the heating chamber 307 is provided with an inlet and outlet for the biomass combustion hot gas 114. The reaction tube is a curved tube in which U-shaped, inverted U-shaped and U-shaped tubes are connected, and includes a first vertical portion, a second vertical portion, a third vertical portion, and a fourth vertical portion from the right side. The open end where the reaction water 115 can be introduced from the upper part of the first vertical part at the right end, and the open end where the biomass fine powder 112 can be introduced from the upper part of the second vertical part in the middle connects the second vertical part and the third vertical part in the middle. An opening end for taking out the ash 117 generated by gasification from the bottom of the U-shaped tube is provided, and an opening end for taking out the water-containing product gas 118 generated by the gasification reaction from the fourth vertical portion at the left end, respectively.

ガス化反応設備101は不図示の熱ガス発生炉で生成した、バイオマス燃焼高温ガス114を前記加熱チャンバ307の導入口より導入して、反応管306を外部より加熱し、その内温を800℃以上の適切な温度に維持するよう、バイオマス燃焼高温ガス114(外部加熱ガス)の温度及び流量を調節する。反応水115は第一垂直部の反応水蒸発部301において外部加熱ガスで加熱され水蒸気となり、第二垂直部の1次ガス化部302で上部より導入された、バイオマス微粉112を浮遊させながらガス化させる。この時、水蒸気/バイオマスのモル比が0.4以上となるように反応水115、微粉112の投入量を加減する。ガス化した生成ガスはついで、第三垂直部及び第四垂直部で構成される2次ガス化部303に流れて、少量の副生したタール・煤を分解する。この部分で固形有機物及び炭素は全て分解して、ガス体となり、固体は無機物からなる灰分のみとなり、前記灰取り出し開口端より、灰117を取り出す。生成ガス118は未だ水分と少量のHSとHClを含んだ状態で含水生成ガス118として前記左端第四垂直部開口端より取り出す。 The gasification reaction equipment 101 introduces a biomass combustion hot gas 114 generated in a hot gas generator (not shown) from the introduction port of the heating chamber 307, heats the reaction tube 306 from the outside, and sets the internal temperature to 800 ° C. The temperature and flow rate of the biomass combustion hot gas 114 (externally heated gas) are adjusted so as to maintain the above appropriate temperature. The reaction water 115 is heated by an external heating gas in the reaction water evaporation unit 301 in the first vertical part to become water vapor, and gas is introduced while floating the biomass fine powder 112 introduced from the upper part in the primary gasification unit 302 in the second vertical part. Make it. At this time, the input amounts of the reaction water 115 and fine powder 112 are adjusted so that the water vapor / biomass molar ratio is 0.4 or more. The gasified product gas then flows to a secondary gasification section 303 composed of a third vertical section and a fourth vertical section, and decomposes a small amount of by-produced tars and soot. At this part, the solid organic matter and carbon are all decomposed to form a gas body, and the solid becomes only the ash composed of inorganic matter, and the ash 117 is taken out from the ash take-out opening end. The product gas 118 is taken out from the opening end of the left end fourth vertical portion as the water-containing product gas 118 in a state still containing moisture, a small amount of H 2 S and HCl.

1次ガス化部302の詳細は図示の如く、反応管306の下部付近が、中央に開口部308を持つコニカル(逆円錐台)型整流板307が設けられ、該開口部308から高温蒸気が吹き込まれ、反応管306上部から投入されたバイオマス微粉112を浮遊させた状態でガス化する。1次ガス化即ち本発明の目的とするガス化は1次ガス化領域304で行われ、この領域を過ぎた第三垂直部の上部は2次ガス化領域305として機能し、前記で説明した2次ガス化部303と同様な役割を果たす。   As shown in detail in the figure, the primary gasification unit 302 is provided with a conical (inverted truncated cone) type rectifying plate 307 having an opening 308 in the center near the lower part of the reaction tube 306, and high-temperature steam is generated from the opening 308. The biomass fine powder 112 injected and introduced from the upper part of the reaction tube 306 is gasified in a suspended state. The primary gasification, that is, the gasification targeted by the present invention, is performed in the primary gasification region 304, and the upper portion of the third vertical portion beyond this region functions as the secondary gasification region 305, as described above. It plays the same role as the secondary gasification unit 303.

(実施例3) 図3は本発明のガス化反応設備と1次ガス化部詳細の他の例の概要図である。ガス化反応設備の全体構成は実施例2と同様である。1次ガス化部401詳細の構成が図示のようになっている。即ち、図3右側の1次ガス化部401詳細において、反応管306中には分散管402が送入されている。分散管は微粉送入管より、底部逆コニカルの底面円周に向けて延在する曲面で構成される、内部中空の一端が逆コニカルで閉鎖された、筒体であり、該底部逆コニカルの底面円周に向けて延在する曲面上に複数の噴出口405を有している。 (Example 3) FIG. 3: is a schematic diagram of the gasification reaction equipment of this invention, and another example of the details of a primary gasification part. The overall configuration of the gasification reaction facility is the same as that of the second embodiment. The detailed structure of the primary gasification unit 401 is as shown in the figure. That is, in the details of the primary gasification unit 401 on the right side of FIG. 3, the dispersion tube 402 is fed into the reaction tube 306. The dispersion tube is a cylindrical body composed of a curved surface extending from the fine powder feeding tube toward the bottom circumference of the bottom inverted conical, with one end of the inner hollow closed by the inverted conical, and the bottom inverted conical A plurality of jet openings 405 are provided on a curved surface extending toward the bottom circumference.

前記反応管306に、該分散管402を挿入すると、分散管402の逆コニカル底面円周部付近と、反応管306内壁との間の距離が最も狭小となり、反応管306下部より蒸気など気体を流通させたとき、スロート部403となり、ここから上部に行くに従い、漸次管内壁と分散管42外壁との距離は拡大していくので、ディフューーザ部404となる。従って、前記複数の噴出口405はこのスロート部403付近に設けることが好ましい。   When the dispersion tube 402 is inserted into the reaction tube 306, the distance between the vicinity of the reverse conical bottom surface of the dispersion tube 402 and the inner wall of the reaction tube 306 is the narrowest, and a gas such as steam is passed from the bottom of the reaction tube 306. When it is circulated, it becomes the throat portion 403, and the distance between the inner wall of the pipe and the outer wall of the dispersion pipe 42 gradually increases from here to the upper portion, so that it becomes the diffuser portion 404. Therefore, the plurality of jet ports 405 are preferably provided in the vicinity of the throat portion 403.

かくして、分散管402の微粉送入管よりバイオマス微粉112を送入すると、反応水115の蒸発によって生成した高温蒸気が下部より流れ込み、スロート部403で高速となって、ベンチュリー効果により分散管402内部の微粉112を吸い出してディフューザ部404に分散させる。該分散浮遊した微粉はほとんど瞬時にガス化する。   Thus, when the biomass fine powder 112 is fed from the fine powder feed pipe of the dispersion pipe 402, the high-temperature steam generated by the evaporation of the reaction water 115 flows from the lower part, becomes high speed at the throat portion 403, and the inside of the dispersion pipe 402 due to the venturi effect. The fine powder 112 is sucked out and dispersed in the diffuser unit 404. The dispersed and suspended fine powder is gasified almost instantaneously.

(実施例4) 図4は本発明の多管式ガス化部を有するガス化反応設備101の概要図である。図において、多管式反応管501は実施例2もしくは3の曲管が図右側のA−A’矢視図に示されるように垂直方向に5列並列に、加熱チャンバ内307に配置されており、バイオマス微粉投入口、灰取り出し口、反応水送入口、含水生成ガス取り出し口はそれぞれヘッダ502、503、504、505で5列が連結されている。これにより、処理空間容量が増加し、コンパクトに能力の増強が可能である。 (Example 4) FIG. 4: is a schematic diagram of the gasification reaction equipment 101 which has the multitubular gasification part of this invention. In the figure, a multi-tubular reaction tube 501 is formed by arranging the curved tubes of Example 2 or 3 in the heating chamber 307 in parallel in five rows in the vertical direction as shown in the AA ′ arrow view on the right side of the drawing. In addition, the biomass fines inlet, the ash outlet, the reaction water inlet, and the hydrated product gas outlet are connected in five rows by headers 502, 503, 504, and 505, respectively. As a result, the processing space capacity is increased, and the capacity can be increased in a compact manner.

(実施例5) 図5は本発明の浮遊・外熱式高カロリガスを生成するガス化反応の温度条件とガス組成及び発熱量との関係を示すグラフである。図2に示す装置を用い本発明の浮遊・外熱式高カロリガス化の試験を、水蒸気/バイオマス重量比を2に固定して、各種温度で行い、生成ガスの組成を分析し、生成ガスの発熱量を測定して、反応のマテリアルバランスを求めた。その結果生成ガスは棒グラフに示すガス組成を与え、その発熱量を測定すると、折れ線グラフの熱量であった。 (Example 5) FIG. 5: is a graph which shows the relationship between the temperature conditions, gas composition, and calorific value of the gasification reaction which produces | generates the floating and external heating type high calorie gas of this invention. Using the apparatus shown in FIG. 2, the floating / external heat type high calorie gasification test of the present invention is performed at various temperatures with the water vapor / biomass weight ratio fixed at 2, analyzing the composition of the product gas, The calorific value was measured to determine the material balance of the reaction. As a result, the generated gas gave the gas composition shown in the bar graph, and when the calorific value was measured, it was the calorific value of the line graph.

上記で得られた反応のマテリアルバランスよりガス化反応の経験式を求めると、
1.30.9+0.4H
→0.8H+0.7CO+0.3CH+0.3CO+39.7kcal/mol
であることがわかった。
Finding the empirical formula of gasification reaction from the material balance of the reaction obtained above,
C 1.3 H 2 O 0.9 +0.4 H 2 O
→ 0.8H 2 + 0.7CO + 0.3CH 4 + 0.3CO 2 +39.7 kcal / mol
I found out that

以上詳しく説明したように、本発明によりタール、煤など遊離炭素の発生を伴わない、廃棄物は若干の灰分のみの、クリーンなH、CO、及びCHなどの炭化水素を主成分とする浮遊・外熱式高カロリガス(例えば20MJ/NM)が得られ、ガスエンジン発電と組合すことにより、総合エネルギ効率の高いシステムとすることができる。 As described above in detail, according to the present invention, waste is free from the generation of free carbon such as tar and soot, and the waste is mainly composed of hydrocarbons such as clean H 2 , CO, and CH 4 with only a small amount of ash. Floating / externally heated high calorie gas (for example, 20 MJ / NM 3 ) is obtained, and by combining with gas engine power generation, a system with high total energy efficiency can be obtained.

本発明の浮遊・外熱式高カロリガスを生成するガス化反応設備を中心とする、バイオエネルギ利用システムのフロー図応設備への搬送方法のフロー図Flow diagram of a method for transporting a bioenergy utilization system to a flow response facility centered on a gasification reaction facility that generates floating / externally heated high calorie gas of the present invention 本発明のガス化反応設備と1次ガス化部詳細の一例の概要図Outline diagram of an example of gasification reaction facility and primary gasification section details of the present invention 本発明のガス化反応設備と1次ガス化部詳細の他の例の概要図Schematic diagram of another example of details of gasification reaction facility and primary gasification section of the present invention 本発明のガス化反応設備と多管式ガス化部の概要図Outline diagram of gasification reaction equipment and multi-tube gasification section of the present invention 本発明の浮遊・外熱式高カロリガスを生成するガス化反応の温度条件とガス組成及び発熱量との関係を示すグラフである。It is a graph which shows the relationship between the temperature conditions, gas composition, and calorific value of the gasification reaction which produces | generates the floating and external-heat type high calorie gas of this invention.

符号の説明Explanation of symbols

101…ガス化反応設備
102…粉砕設備
103…熱ガス発生炉
104…脱水装置
105…ガスタンク
106…ガスエンジン
111…バイオマス原料
112…微粉
113…粗分
114…バイオマス燃焼高温ガス
115…反応水
116…生成ガス
211…蒸気又は蒸気+少量空気
301…反応水蒸発部
302…1次ガス化部
303…2次ガス化部
304…1次ガス化域
305…2次ガス化域
306…反応管
307…加熱チャンバ
401…1次ガス化部
402…分散管
403…スロート部
404…ディフューザ部
501…多管式反応管
502…ヘッダ
503…ヘッダ
504…ヘッダ
505…ヘッダ
DESCRIPTION OF SYMBOLS 101 ... Gasification reaction equipment 102 ... Grinding equipment 103 ... Hot gas generator 104 ... Dehydration apparatus 105 ... Gas tank 106 ... Gas engine 111 ... Biomass raw material 112 ... Fine powder 113 ... Coarse content 114 ... Biomass combustion hot gas 115 ... Reaction water 116 ... Product gas 211 ... Steam or steam + small amount air 301 ... Reaction water evaporation section 302 ... Primary gasification section 303 ... Secondary gasification section 304 ... Primary gasification section 305 ... Secondary gasification section 306 ... Reaction tube 307 ... Heating chamber 401 ... Primary gasification unit 402 ... Dispersion tube 403 ... Throat unit 404 ... Diffuser unit 501 ... Multi-tube reaction tube 502 ... Header 503 ... Header 504 ... Header 505 ... Header

Claims (6)

粉砕した草本類若しくは木本類からなるバイオマス微粉を、外部加熱空間と隔壁により遮断されたガス化空間内に供給して、且つ前記外部加熱空間より隔壁を介して加熱して、吸熱反応によりガス化空間内で、該ガス化空間内に吹き込まれる高温水蒸気とバイオマスのガス化反応を生じせしめるバイオマスのガス化方法であって、前記バイオマスの分子式CmHOnにおいて、m=1.3、n=0.9とした場合の、前記高温水蒸気/バイオマスのモル比を0.3〜15に設定したことを特微とするバイオマスのガス化方法。 The biomass fine powder made of pulverized herb or wood is supplied into the gasification space blocked by the external heating space and the partition wall, and is heated through the partition wall from the external heating space, and gas is absorbed by an endothermic reaction. A biomass gasification method for generating a gasification reaction between biomass and high-temperature steam blown into the gasification space, wherein m = 1.3, n = in the molecular formula CmH 2 On of the biomass A biomass gasification method characterized in that, when 0.9, the high-temperature steam / biomass molar ratio is set to 0.3 to 15. 前記外部加熱空間より加える熱量が25Kcal/バイオマスモル以上であることを特微とする請求項1記載のバイオマスのガス化方法。   2. The biomass gasification method according to claim 1, wherein the amount of heat applied from the external heating space is 25 Kcal / biomass mole or more. 外部より隔壁を介してガス化空間内の前記バイオマスに加える熱量がガス化反応後にすす若しくはタールが生じないようにガス化空間内の水蒸気の熱量及び隔壁からの外部熱量を調整して供給することを特微とする請求項1記載のバイオマスのガス化方法。   Adjusting and supplying the heat quantity of water vapor in the gasification space and the external heat quantity from the partition walls so that the amount of heat applied to the biomass in the gasification space from the outside through the partition walls does not generate soot or tar after the gasification reaction The biomass gasification method according to claim 1, characterized in that: 請求項1記載のバイオマスのガス化方法において、下記(1)式の条件を満たすように、前記水蒸気/バイオマスのモル比と外部加熱空間よりの外部加熱カロリ及びガス化空間の還元雰囲気を設定したことを特微とするバイオマスのガス化方法。
1.30.9+p
→q+qCO+qCH+qCO…(1)
The biomass gasification method according to claim 1, wherein the steam / biomass molar ratio, the external heating calorie from the external heating space, and the reducing atmosphere of the gasification space are set so as to satisfy the following formula (1). This is a method for gasifying biomass.
C 1.3 H 2 O 0.9 + p 1 H 2 O
→ q 1 H 2 + q 2 CO + q 3 CH 4 + q 4 CO 2 (1)
炉内ガス化温度が800〜1000℃で、且つガス化雰囲気が常圧下で触媒を用いない還元性雰囲気であることを特微とする請求項1、3若しくは4記載のバイオマスのガス化方法。   The method for gasifying biomass according to claim 1, 3 or 4, wherein the gasification temperature in the furnace is 800 to 1000 ° C, and the gasification atmosphere is a reducing atmosphere that does not use a catalyst under normal pressure. 粉砕した草本類若しくは木本類からなるバイオマスに、水蒸気を供給してガス化反応を生じせしめるガス化空間が、隔壁を構成する金属反応管を介して外部加熱空間と遮断され、前記金属反応管の管壁を介してガス化空間に幅射熱が付与されるようにしたことを特微とする請求項1記載のバイオマスのガス化方法。   A gasification space in which water vapor is supplied to the crushed herbaceous or woody biomass to cause a gasification reaction is cut off from an external heating space via a metal reaction tube constituting a partition wall, and the metal reaction tube The biomass gasification method according to claim 1, wherein width radiation heat is applied to the gasification space through the tube wall.
JP2008225517A 2008-09-03 2008-09-03 Biomass gasification method Expired - Lifetime JP4665021B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2008225517A JP4665021B2 (en) 2008-09-03 2008-09-03 Biomass gasification method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008225517A JP4665021B2 (en) 2008-09-03 2008-09-03 Biomass gasification method

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2002208964A Division JP4227771B2 (en) 2002-07-17 2002-07-17 Biomass gasification method

Publications (2)

Publication Number Publication Date
JP2009001826A true JP2009001826A (en) 2009-01-08
JP4665021B2 JP4665021B2 (en) 2011-04-06

Family

ID=40318533

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008225517A Expired - Lifetime JP4665021B2 (en) 2008-09-03 2008-09-03 Biomass gasification method

Country Status (1)

Country Link
JP (1) JP4665021B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013094382A1 (en) * 2011-12-20 2013-06-27 学校法人長崎総合科学大学 Method and device for producing synthetic gas and method and device for synthesizing liquid fuel
JP2015534534A (en) * 2012-09-18 2015-12-03 プロトン パワー, インク.Proton Power, Inc. C—O—H compound treatment to produce hydrogen or liquid fuel
US9226932B2 (en) 2005-06-29 2016-01-05 Threshold Pharmaceuticals, Inc. Phosphoramidate alkylator prodrugs
CN111380391A (en) * 2020-02-28 2020-07-07 杭州中亚机械股份有限公司 Gasification part and gasification system

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0741767A (en) * 1993-07-26 1995-02-10 Osaka Gas Co Ltd Thermal decomposition of biomass
JPH07138580A (en) * 1993-11-19 1995-05-30 Mitsubishi Heavy Ind Ltd Gasification of organic matter
JP2001115174A (en) * 1999-10-15 2001-04-24 Toshiba Corp Fuel treatment system
JP2001240877A (en) * 2000-02-29 2001-09-04 Mitsubishi Heavy Ind Ltd Biomass-gasifying furnace and method of gasifying biomass
JP2001354974A (en) * 2000-06-13 2001-12-25 Toshiba Corp Fuel gasification method and its apparatus

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0741767A (en) * 1993-07-26 1995-02-10 Osaka Gas Co Ltd Thermal decomposition of biomass
JPH07138580A (en) * 1993-11-19 1995-05-30 Mitsubishi Heavy Ind Ltd Gasification of organic matter
JP2001115174A (en) * 1999-10-15 2001-04-24 Toshiba Corp Fuel treatment system
JP2001240877A (en) * 2000-02-29 2001-09-04 Mitsubishi Heavy Ind Ltd Biomass-gasifying furnace and method of gasifying biomass
JP2001354974A (en) * 2000-06-13 2001-12-25 Toshiba Corp Fuel gasification method and its apparatus

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9226932B2 (en) 2005-06-29 2016-01-05 Threshold Pharmaceuticals, Inc. Phosphoramidate alkylator prodrugs
WO2013094382A1 (en) * 2011-12-20 2013-06-27 学校法人長崎総合科学大学 Method and device for producing synthetic gas and method and device for synthesizing liquid fuel
JPWO2013094382A1 (en) * 2011-12-20 2015-04-27 学校法人長崎総合科学大学 Syngas production method and production apparatus, and liquid fuel synthesis method and synthesis apparatus
JP2015534534A (en) * 2012-09-18 2015-12-03 プロトン パワー, インク.Proton Power, Inc. C—O—H compound treatment to produce hydrogen or liquid fuel
CN111380391A (en) * 2020-02-28 2020-07-07 杭州中亚机械股份有限公司 Gasification part and gasification system

Also Published As

Publication number Publication date
JP4665021B2 (en) 2011-04-06

Similar Documents

Publication Publication Date Title
JP4986080B2 (en) Biomass gasifier
RU2526387C1 (en) Method and device for low-temperature biomass pyrolysis and high-temperature biomass gasification
Natarajan et al. Overview of combustion and gasification of rice husk in fluidized bed reactors
JP4267968B2 (en) Biomass processing method
US10035963B2 (en) Biomass high efficiency hydrothermal reformer
WO2017050231A1 (en) Industrial furnace integrated with biomass gasification system
TW201009066A (en) Process and device for the production of low-tar synthesis gas from biomass
RU2333929C1 (en) Method and device for hard fuel gasification
KR20120004979A (en) Two stage dry feed gasification system and process
JP5316948B2 (en) Biomass pyrolysis equipment
JP4227771B2 (en) Biomass gasification method
JP7140341B2 (en) Hydrogen production method using biomass as raw material
CA2727395C (en) Method and equipment for producing synthesis gas
KR20210083317A (en) Systems and methods for treating carbonaceous feedstock
JP4665021B2 (en) Biomass gasification method
US9643885B2 (en) Method and arrangement for burning lime mud
JP2004051717A (en) Biomass gasifier
WO2010063205A1 (en) High temperature gasifying process with biomass and system thereof
JP3559163B2 (en) Gasification method using biomass and fossil fuel
JP2009102594A (en) Gasification furnace system
JP6590359B1 (en) Hydrogen production method using biomass as raw material
EP4121495A1 (en) Tar free cross flow gasification system for moisture containing feed
JP2004182903A (en) Method and apparatus for gasifying biomass
JP2009235189A (en) Method for gasifying woody or agricultural biomass
JP7291677B2 (en) Water gas generation system, biomass power generation system and biomass hydrogen supply system

Legal Events

Date Code Title Description
A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20100915

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100924

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20101122

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: 20101222

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20110107

R150 Certificate of patent or registration of utility model

Ref document number: 4665021

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

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

Free format text: PAYMENT UNTIL: 20140114

Year of fee payment: 3

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

EXPY Cancellation because of completion of term