JP2001098271A - Ground solidification material - Google Patents
Ground solidification materialInfo
- Publication number
- JP2001098271A JP2001098271A JP27647399A JP27647399A JP2001098271A JP 2001098271 A JP2001098271 A JP 2001098271A JP 27647399 A JP27647399 A JP 27647399A JP 27647399 A JP27647399 A JP 27647399A JP 2001098271 A JP2001098271 A JP 2001098271A
- Authority
- JP
- Japan
- Prior art keywords
- cement
- fine particle
- silica sol
- ground
- amount
- 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
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/91—Use of waste materials as fillers for mortars or concrete
Landscapes
- Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は中性シリカゾル・微
粒子セメント系の懸濁型地盤固結材に係り、特に、浸透
可能時間が長くて浸透性に優れ、かつ高固結強度を呈す
る地盤固結材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a suspension type soil compaction material of a neutral silica sol / fine particle cement system, and more particularly to a soil compaction material having a long permeation time, excellent permeability, and exhibiting high compaction strength. Regarding binder.
【0002】[0002]
【従来の技術】地盤を製造するための地盤注入用のグラ
ウトとして従来、種々のものが知られている。例えば、
モル比が小さくアルカリ度の高い水ガラスを用いるスラ
グ系のグラウトが知られている。このグラウトは固結強
度が大きいがアルカリの溶脱が懸念される。また中性シ
リカゾルに多価金属塩を加えた溶液型グラウトも知られ
ているが、これは固結強度が小さいという欠点があっ
た。この強度を解決するために近年、中性シリカゾルと
ポルトランドセメントを1.5ショットで合流して注入
する方法も知られているが、このグラウトのゲル化時間
はせいぜい1分以内と短く、浸透性に劣るものである。
さらにまた、中性シリカゾルに高炉スラグおよびポルト
ランドセメントを添加してなるグラウトも知られてい
る。しかし、このような中性シリカゾルを使用したグラ
ウトは、地上でカップ倒立法により測定したゲル化時間
が10分以内と短いばかりか、土中ではゲル化時間がさ
らに短くなるため、浸透が悪く、土粒子間で目詰まりを
おこしてしまう。さらに、ゲル化させることの出来ない
材料を使用した地盤固結材としては、セメント/ベント
ナイト懸濁液、スラグ−アルカリ刺激剤(水ガラスを除
く)懸濁液等が知られている。しかしながら、これらは
いずれも配合液の粘度を短時間に増加させることは出来
ず、限定注入が難しいとされてきた。なお、少量の水ガ
ラスをセメント懸濁液と混合すると、10秒程度でチク
ソ性の懸濁液となるため、このような配合液は裏込材と
して使用されていることがあるが、本発明の配合液とは
全く異なるものである。2. Description of the Related Art Conventionally, various grouts have been known as grouts for injecting ground into a ground. For example,
A slag grout using water glass having a small molar ratio and high alkalinity is known. Although this grout has a high consolidation strength, there is concern about leaching of alkali. A solution type grout in which a polyvalent metal salt is added to a neutral silica sol is also known, but this has a drawback that the compaction strength is small. In order to solve this strength, a method has recently been known in which neutral silica sol and Portland cement are combined at 1.5 shots and injected, but the gelation time of this grout is as short as 1 minute at most, and the permeability is low. It is inferior to.
Further, a grout obtained by adding blast furnace slag and Portland cement to neutral silica sol is also known. However, the grout using such a neutral silica sol is not only short of the gelation time measured by the cup inverted method on the ground as less than 10 minutes, but also the gelation time is further shortened in the soil, so that the penetration is poor, Clogging occurs between soil particles. Further, as a ground consolidation material using a material that cannot be gelled, a cement / bentonite suspension, a slag-alkali stimulant (excluding water glass) suspension and the like are known. However, none of them can increase the viscosity of the blended liquid in a short time, and it has been considered that limited injection is difficult. When a small amount of water glass is mixed with a cement suspension, the mixture becomes a thixotropic suspension in about 10 seconds. Therefore, such a mixed solution is sometimes used as a backing material. Is completely different from the liquid mixture of the above.
【0003】[0003]
【発明が解決しようとする課題】本発明者らは上記課題
を解決すべく鋭意研究の結果、特定の中性シリカゾル
と、微粒子セメントと、必要に応じてスラグとを所望の
条件下で配合すると、配合液は次第に増粘して可塑状態
を保持するようになるが、明確なゲル化時間を呈さなく
することが出来る。このような配合液は、増粘時間の調
整が容易であって浸透時間を長くすることもでき、従っ
て浸透性がよく、しかも注入完了後には流動性を失って
実質的に固結し、ゲル化時間を呈するグラウトと同様な
効果を奏しうることを発見し、本発明を完成するに至っ
た。本発明の目的は浸透可能時間が長くて浸透性に優
れ、しかも高固結強度を呈し、かつアルカリ溶脱が少な
いため、固結物が耐久性に優れているばかりか、環境へ
の影響も少なく、上述の公知技術に存する欠点を改良し
た中性シリカゾル・微粒子セメント系の懸濁型地盤固結
材を提供することにある。The present inventors have conducted intensive studies to solve the above-mentioned problems. As a result, the present inventors have found that a specific neutral silica sol, fine particle cement, and, if necessary, slag are blended under desired conditions. Although the compounded liquid gradually increases in viscosity and keeps a plastic state, it is possible to eliminate a definite gelation time. Such a blended liquid is easy to adjust the thickening time and can extend the permeation time, so that it has good permeability, and after the injection is completed, loses fluidity and substantially solidifies, and the gel is gelled. It has been discovered that the same effect as a grout exhibiting an aging time can be obtained, and the present invention has been completed. The object of the present invention is that the permeation time is long, the permeability is excellent, and high consolidation strength is exhibited, and there is little alkali leaching, so that the consolidation is not only excellent in durability but also has little effect on the environment. It is another object of the present invention to provide a neutral silica sol / particulate cement type suspension-type ground consolidating material in which the disadvantages of the above-mentioned known technology are improved.
【0004】[0004]
【課題を解決するための手段】上述の目的を達成するた
め、本発明の地盤固結材は、水ガラスのアルカリの大部
分をイオン交換樹脂で除去し、造粒して得られた中性シ
リカゾルと、微粒子セメント更に必要に応じて用いられ
るスラグを有効成分とし、前記中性シリカゾルの含有量
が全配合液中の0.5〜5容量%(SiO2 濃度30%
のシリカゾル換算)であることを特徴とする。In order to achieve the above-mentioned object, the ground consolidating material of the present invention is obtained by removing most of the alkali of water glass with an ion exchange resin and granulating the neutralized water. Silica sol, fine particle cement and slag used as necessary are used as active ingredients, and the content of the neutral silica sol is 0.5 to 5% by volume (SiO 2 concentration 30%
In terms of silica sol).
【0005】[0005]
【発明の実施の形態】以下、本発明を具体的に詳述す
る。本発明に係る地盤固結材は、配合後次第に増粘し、
やがて粘度が高くなると可塑状態を保つがゲル化は起こ
さない。ここで増粘時間は1分以上、好ましくは10〜
120分程度が適当であり、その後可塑状態を10分以
上、好ましくは30分以上保ち続ける。この様な本発明
に係る配合液を地盤に注入すると、地盤が密な場合には
増粘段階で従来のゲル化と同様の効果を発揮して、配合
液は浸透しなくなり、地盤が粗な場合には増粘段階から
可塑状態でも注入(浸透)が継続される。ここで、従来
の地盤固結材では、カップ倒立法でゲル化時間を測定
し、カップを傾けても流れ出なくなった時間を「ゲル化
時間」としているのに対し、本発明の配合液を、B型粘
度計で測定すると、概略500cps(センチポイズ)
以上となるが、約1,000cps以下であり、カップ
倒立法で測定してもカップから流れ出なくなるというこ
とがないため、B型粘度計で測定して、配合液調製時か
ら粘度が500cpsとなるまでの経過時間を「増粘時
間」とする。なお、懸濁液をB型粘度計で測定すること
には若干の問題があるが、従来のゲル化する型の地盤固
結材は、その配合液の粘度をB型粘度計で測定すると、
増粘し始めると急激に2,000cps以上と高粘度に
なりゲル化してしまうので、本発明ではB型粘度計で測
定した値を1つの目安とした。また、上記のように、
「ゲル化」とは液状である配合液が、反応により保形性
を有するようになることであり、具体的には上記のよう
にカップ倒立法で測定して、カップを傾けても流れ出な
くなった状態をいう。このような配合液はゲル化すると
全く浸透しなくなるのであり、可塑状態を保持するが、
ゲル化しない本発明の配合液とは全く異なるのである。
なお、カップ倒立法でゲル化しない配合でも土中に注入
した後、土粒子間にあって外力が加えられなければ、次
第に固化(あるいは固結)するが、これは本発明の「明
白なゲル化状態にならない」には該当しない。なお、増
粘時間が10分以上の配合は、殆ど可塑状態が10分以
上継続する。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. The ground consolidated material according to the present invention gradually thickens after being blended,
As the viscosity increases, the plastic state is maintained, but no gelation occurs. Here, the thickening time is 1 minute or more, preferably 10 to
About 120 minutes is appropriate, and thereafter the plastic state is maintained for 10 minutes or more, preferably 30 minutes or more. When such a mixed solution according to the present invention is injected into the ground, when the ground is dense, the same effect as in the conventional gelation is exerted at the thickening stage, the mixed solution does not penetrate, and the ground is rough. In this case, the injection (penetration) is continued even in the plastic state from the thickening stage. Here, in the conventional ground consolidation material, the gelation time is measured by the cup inversion method, and the time at which the cup does not flow even when the cup is tilted is referred to as `` gelation time '', whereas the compounded liquid of the present invention is Approximately 500 cps (centipoise) when measured with a B-type viscometer
As described above, the viscosity is about 1,000 cps or less, and it does not flow out of the cup even when measured by the cup inversion method. The elapsed time up to this point is referred to as “thickening time”. There are some problems in measuring the suspension with a B-type viscometer, but the conventional gel-forming type ground consolidating material has a viscosity of the compounded liquid measured with a B-type viscometer.
When the viscosity starts to increase, the viscosity rapidly increases to 2,000 cps or more and gels. Therefore, in the present invention, a value measured by a B-type viscometer was used as one standard. Also, as mentioned above,
"Gelling" means that the liquid compound liquid has a shape-retaining property due to the reaction.Specifically, it is measured by the cup inversion method as described above, and it does not flow even if the cup is tilted. State. Such a mixed solution does not penetrate at all when it gels, and maintains a plastic state,
This is completely different from the formulation of the present invention which does not gel.
It should be noted that even if the composition is not gelled by the cup inversion method, it is gradually solidified (or solidified) after being poured into the soil if no external force is applied between the soil particles. Does not fall under. In addition, when the thickening time is 10 minutes or more, almost the plastic state continues for 10 minutes or more.
【0006】また「可塑状態」とは注入等による外力が
加えられると流動性を示すが、外力がなくなると流動性
を示さない状態をいう。配合時にこのような可塑状態に
なると浸透性が悪くなるので、このような場合は本発明
の範囲から除外し、少なくとも1分以上経過後に可塑状
態となることが必要である。また可塑状態の継続時間が
短い場合には、その後ゲル化する場合もありうるので可
塑状態が少なくとも10分以上、好ましくは60分以上
持続することが必要であり、その後は静置等により固化
しても本発明の目的が達成されることに変わりはない。[0006] The "plastic state" refers to a state in which fluidity is exhibited when an external force due to injection or the like is applied, but is not exhibited when the external force is removed. Since such a plasticized state at the time of compounding deteriorates permeability, such a case is excluded from the scope of the present invention, and it is necessary that the plasticized state be obtained after at least one minute has passed. If the duration of the plastic state is short, the plastic state may last at least 10 minutes or more, preferably 60 minutes or more, since gelling may occur thereafter. However, the object of the present invention is still achieved.
【0007】上述の本発明は、中性シリカゾルと、微粒
子セメント好ましくは微粒子スラグを併用した地盤固結
材であって、中性シリカゾルの使用量が配合液を増粘さ
せるに必要な量、即ち配合液全体の0.5〜5容量%で
あり、微粒子セメントが好ましくはブレーン比表面積
4,000cm2/g 以上であることを特徴とし、必要に応
じて増粘時間の調整剤を添加することも出来る。さらに
説明すると、配合液がゲル化しない場合は問題がない
が、見かけ上ゲル状態となっている場合には、セメント
の固化が始まらないうちにその強度を測定し0.1kgf/cm2
以下であれば、ほぼ攪拌によってこわれるような弱いゲ
ルであり、このような配合は本発明の範囲に入るものと
する。すなわち、上記中性シリカゾルの配合量は、配合
液が増粘するが水ガラス溶液型グラウトのホモゲルの様
な弾力性のあるゲルが出来ない量であり、微粒子セメン
トの粒度及び微粒子スラグの併用、更には増粘時間の調
整剤の添加量によっても異なる。The present invention described above relates to a ground consolidation material using a neutral silica sol in combination with a fine particle cement, preferably a fine particle slag, wherein the amount of the neutral silica sol used is an amount necessary to thicken the blended liquid, that is, 0.5 to 5% by volume of the total blended liquid, and the fine particle cement preferably has a Blaine specific surface area of 4,000 cm 2 / g or more, and if necessary, a thickening time modifier is added. You can also. To explain further, there is no problem when the blended liquid does not gel, but when it is apparently in a gel state, its strength is measured before the solidification of the cement starts and 0.1 kgf / cm 2
If it is below, it is a weak gel which is almost broken by stirring, and such a composition is within the scope of the present invention. That is, the blending amount of the neutral silica sol is such that the blending solution thickens but an elastic gel such as a homogel of a water glass solution type grout cannot be formed, and the particle size of the fine particle cement and the fine particle slag are used in combination. Furthermore, it depends on the amount of the thickening time regulator added.
【0008】浸透可能時間については、地盤の状況によ
り異なるため明確なことは言えないが、一般的な中性シ
リカゾルを使用した従来のシリカゾル・セメント系グラ
ウトではゲル化時間の調整剤を添加してもゲル化時間が
約10分以下(特に夏場では3分以下であり、セメント
に超微粒子セメントを使用した場合には10秒以下と極
めて短く、これを長くすることは殆ど不可能である)と
極めて短いばかりか、増粘開始後ゲル化が急激に起こ
り、しかもゲル化後はゲル強度が大きいためそれ以上ゲ
ルを破壊して浸透させることが出来ない。[0008] The infiltration time is not clear because it depends on the condition of the ground. However, in a conventional silica sol-cement grout using a general neutral silica sol, a gel time adjustment agent is added. Also, the gel time is about 10 minutes or less (especially 3 minutes or less in summer, and extremely short as 10 seconds or less when using ultrafine cement for cement, and it is almost impossible to lengthen this). Not only is it extremely short, but gelation occurs rapidly after the start of thickening, and the gel strength is high after gelation, so that the gel cannot be further broken and penetrated.
【0009】これに対し、本発明にかかる地盤固結材は
増粘時間を1時間以上にもすることが出来、しかもいわ
ゆるゲル強度(本発明では可塑状態となっているためゲ
ル強度とはいわない)が弱いため増粘時間経過後も地盤
によっては浸透可能であり、このように、浸透可能時間
を十分長くすることが出来る。On the other hand, the ground consolidation material according to the present invention can have a thickening time of 1 hour or more, and has a so-called gel strength. No) can be penetrated depending on the ground even after the elapse of the thickening time, and thus the permeation possible time can be sufficiently lengthened.
【0010】またセメントを単独の懸濁液で注入する
と、セメントが目詰まりをしたり沈降するのに対し、本
発明の地盤固結材は、中性シリカゾル中のシリカがセメ
ント粒子に付着して、該セメント粒子の潤滑性(目詰ま
りしないで砂の間隙を通過すること)を良好にするため
か浸透性がよく、その後の増粘により注入液のほぼ全体
が固化する。When the cement is injected as a single suspension, the cement is clogged or settles. On the other hand, in the ground consolidating material of the present invention, the silica in the neutral silica sol adheres to the cement particles. In order to improve the lubricity of the cement particles (pass through the gaps of the sand without clogging), the cement particles have good permeability, and the subsequent thickening hardens almost the entire injection liquid.
【0011】本発明で用いられる中性シリカゾルは、水
ガラスをイオン交換樹脂で処理してNa+ イオン等のア
ルカリを殆ど分離除去し、粒径が6〜50ミリミクロン
の大きさに加熱造粒して得られた半透明の液体で、中性
〜弱アルカリ性、好ましくはpHが8.0〜10.5の
弱アルカリ性で、比重が1.16〜1.24で、おおよ
そSiO2 が10〜40重量%、Na2 Oが0.01〜
4重量%の範囲にあるものである。Na2 Oが4重量%
以上になると珪酸コロイドは溶けてしまい珪酸塩の水溶
液となってしまう。一方Na2 Oが0.01重量%以下
になると珪酸コロイドは安定して存在し得ず凝集してし
まう。即ちNa2 Oが0.01〜4重量%の範囲でNa
イオンが珪酸コロイドの表面に分布して安定したコロイ
ド状に保ちうる。この場合、珪酸コロイドの粒径はほぼ
6〜50ミリミクロンが主となる。珪酸コロイドの粒径
が50ミリミクロン以上になると沈澱してしまう。以上
の珪酸コロイドは、モル比(SiO2 /Na2 O)でほ
ぼ10〜1,000とし、pHは8〜10がコロイドの
安定上望ましい。このようにして調製された珪酸コロイ
ドは半永久的に安定しており、これを工場から現場への
搬入並びに注入操作の際にゲル化する心配がない。The neutral silica sol used in the present invention is prepared by treating water glass with an ion-exchange resin to substantially separate and remove alkali such as Na + ions, and heat granulating to a particle size of 6 to 50 mm. The translucent liquid obtained above is neutral to weakly alkaline, preferably weakly alkaline having a pH of 8.0 to 10.5, has a specific gravity of 1.16 to 1.24, and has a SiO 2 of approximately 10 to 10. 40 wt%, Na 2 O is 0.01
It is in the range of 4% by weight. 4% by weight of Na 2 O
When the above is reached, the silicate colloid dissolves and becomes an aqueous solution of silicate. On the other hand, when the content of Na 2 O is 0.01% by weight or less, the silicate colloid cannot exist stably and aggregates. That is, when Na 2 O is in the range of 0.01 to 4% by weight,
The ions can be distributed on the surface of the silicate colloid to maintain a stable colloidal state. In this case, the particle size of the silicate colloid is mainly about 6 to 50 mm. When the particle size of the silicate colloid becomes 50 millimicrons or more, it precipitates. The above silicic acid colloid has a molar ratio (SiO 2 / Na 2 O) of about 10 to 1,000, and a pH of 8 to 10 is desirable for the stability of the colloid. The silicate colloid prepared in this manner is semi-permanently stable, and there is no concern that the silicate colloid will be gelled when it is transported from the factory to the site and when it is injected.
【0012】本発明で用いられる微粒子セメントは、浸
透性の点からブレーン比表面積4,000cm2/g 以上で
あることが好ましい。増粘時間をより長くする場合に
は、特に微粒子セメント量を少なくする。また、中性シ
リカゾルの使用量が比較的多く、ゲル化し易い場合にこ
れをゲル化しない配合とするには、微粒子スラグを併用
するとよい。併用される微粒子スラグのブレーン比表面
積は、8,000cm2/g以上、好ましくは10,000c
m2 /g以上である。固結物の強度は用途に応じて適宜選
択出来るが、微粒子セメントの使用量は、地盤固結材
1,000ml当たり30〜300gが好ましい。とくに
高強度、耐久性の固結物を得るためには、微粒子セメン
トの量は地盤固結材1,000ml当たり50g以上が好
ましく、微粒子スラグを併用することが好ましい。この
場合、微粒子セメントと微粒子スラグの比率を100〜
20:0〜80で使用することが好ましい。The fine particle cement used in the present invention preferably has a Blaine specific surface area of 4,000 cm 2 / g or more from the viewpoint of permeability. When the thickening time is made longer, the amount of the fine particle cement is particularly reduced. Further, when the amount of the neutral silica sol used is relatively large and gelation is likely to occur, a fine particle slag may be used in combination in order to make the mixture not gelled. The Blaine specific surface area of the fine particle slag used in combination is 8,000 cm 2 / g or more, preferably 10,000 c 2 / g.
m 2 / g or more. The strength of the solidified material can be appropriately selected according to the application, but the amount of the fine particle cement used is preferably 30 to 300 g per 1,000 ml of the ground solidified material. In particular, in order to obtain a high-strength and durable compact, the amount of the fine-particle cement is preferably 50 g or more per 1,000 ml of the ground consolidating material, and the fine-particle slag is preferably used in combination. In this case, the ratio of the fine particle cement and the fine particle slag is 100 to
It is preferably used at 20: 0 to 80.
【0013】また、従来懸濁型固結材のみを注入した場
合には、地下水面下では湧水のため掘削が出来ない場合
が多く、溶液型注入材を併用して止水を行っていた。と
ころが、本発明の地盤固結材は浸透性が良く、固結物の
透水係数が小さいために、単独で注入した場合でも湧水
のトラブルがなく、掘削ができるのである。[0013] Conventionally, when only suspension-type consolidation material is injected, excavation cannot often be performed under groundwater due to spring water, and water is stopped using a solution-type injection material in combination. . However, since the ground consolidation material of the present invention has good permeability and low permeability of the consolidation material, even when injected alone, there is no spring water trouble and excavation can be performed.
【0014】このような本発明にかかる中性シリカゾル
・微粒子セメント系では、中性シリカゾル、微粒子セメ
ントの使用量を変えることにより増粘時間を調整するこ
とが出来るが、さらに増粘時間の調整剤を添加すること
により増粘時間を遅延せしめるとともに、配合液を低粘
度化することにより、浸透性の向上をはかることができ
る。短い時間でゲル化するような場合には、増粘時間の
調整剤を添加することにより、増粘はするがゲル化はし
なくする。In the neutral silica sol / fine particle cement system according to the present invention, the thickening time can be adjusted by changing the amount of the neutral silica sol and fine particle cement. In addition to delaying the thickening time by adding the compound, the permeability can be improved by lowering the viscosity of the blended liquid. In the case where gelation occurs in a short time, a thickening time adjusting agent is added to increase the viscosity but not to gel.
【0015】増粘時間の調整剤の使用量は、地盤注入材
の使用条件、特に液温によって適宜選択することが出来
るが、増粘時間を30分以上、必要に応じては数時間と
出来ることが本発明の特徴であり、そのような場合には
増粘時間の調整剤を微粒子セメントに対し0.1〜10
重量%使用することが出来る。上述増粘時間の調整剤と
しては、アルカリ金属の重炭酸塩、炭酸塩、燐酸塩、酸
性燐酸塩、ピロ燐酸塩、クエン酸、酒石酸およびリグニ
ンスルホン酸ソーダ、ポリスルホン酸ソーダ等の(遅延
型)セメント流動化剤等が挙げられる。これらのうちで
特に、好ましい調整剤としては、固結物の強度への影響
の少ないアルカリ金属の重炭酸塩、炭酸塩等である。こ
のような増粘時間の調整剤は中性シリカゾルの側に添加
し、注入時に微粒子セメントの懸濁液と混合すると、セ
メントの凝集物が出来ず、懸濁液中の粒子の粒径が小さ
く、液の粘度も小さいため浸透性がより良好となる。The amount of the thickening time adjusting agent can be appropriately selected depending on the use conditions of the ground injection material, particularly the liquid temperature, but the thickening time can be 30 minutes or more, and if necessary, several hours. It is a feature of the present invention, in such a case, the thickening time regulator is added to the fine particle cement 0.1 to 10
% By weight. Examples of the thickening time regulator include alkali metal bicarbonates, carbonates, phosphates, acid phosphates, pyrophosphates, citric acid, tartaric acid and sodium ligninsulfonate and sodium polysulfonate (delayed type). And cement fluidizing agents. Among these, particularly preferred modifiers are alkali metal bicarbonates, carbonates, and the like, which have little effect on the strength of the consolidated product. When such a thickening time modifier is added to the neutral silica sol side and mixed with the suspension of fine cement at the time of injection, aggregates of the cement cannot be formed, and the particle size of the particles in the suspension is small. Also, since the viscosity of the liquid is small, the permeability is better.
【0016】なお、水ガラスからイオン交換樹脂で脱ア
ルカリして得られる活性シリカは、炭酸水素ナトリウム
と混合しただけでゲル化するのであり、ゲル化する前に
上記使用量の活性シリカとセメント懸濁液を混合して
も、本発明の中性シリカゾルを使用した場合のように可
塑状態とはならない。The active silica obtained by dealkalizing water glass with an ion exchange resin gels only by mixing it with sodium bicarbonate. Even if the suspension is mixed, it does not become in a plastic state as in the case of using the neutral silica sol of the present invention.
【0017】また、セメント流動化剤を添加する場合に
は、微粒子セメント側に添加した方が好ましく、その場
合には他の調整剤を中性シリカゾル側に添加するのが好
ましい。調整剤を添加する場合、予め水に溶解した後中
性シリカゾルを添加する方法が好ましく、その状態で均
一であるような調整剤を選択使用することが好ましい。
さらに増粘時間の調整剤を添加することにより、A,B
両液混合時の粘度が小さくなり、浸透性をより高めるこ
とが出来る。When a cement fluidizer is added, it is preferable to add it to the fine particle cement side, and in that case, it is preferable to add another modifier to the neutral silica sol side. When adding a regulator, a method of dissolving in advance in water and then adding a neutral silica sol is preferable, and it is preferable to select and use a regulator which is uniform in that state.
Further, by adding a thickening time regulator, A, B
The viscosity at the time of mixing the two liquids is reduced, and the permeability can be further increased.
【0018】本発明の配合液の具体的な調製法について
さらに詳述する。まず、固結物の強度からセメント、ス
ラグの比表面積およびその使用量を決定する。ついで中
性シリカゾルの使用量をシリカ濃度が0.5〜5容量%
となるようにする。中性シリカゾルのこの範囲において
も配合液がゲル化する場合には、増粘時間の調整剤を添
加する。A specific method for preparing the liquid mixture of the present invention will be described in more detail. First, the specific surface area of cement and slag and the amount used thereof are determined from the strength of the solidified material. Then, the used amount of the neutral silica sol is adjusted so that the silica concentration is 0.5 to 5% by volume.
So that If the mixed solution gels even in this range of the neutral silica sol, a thickening time regulator is added.
【0019】本発明の地盤固結材を注入する場合に、一
次注入材としてゲル化時間の短い溶液型あるいは懸濁型
の注入材を注入して地上への漏出を防止あるいは粗な部
分に充填して本発明の固結材の逸走を防止した後、本発
明の地盤固結材を注入してもよい。When the ground consolidation material of the present invention is injected, a solution type or suspension type injection material having a short gelation time is injected as a primary injection material to prevent leakage to the ground or to fill a rough portion. Then, after the escape of the consolidated material of the present invention is prevented, the ground consolidated material of the present invention may be injected.
【0020】また、本発明の地盤固結材は、低粘度で浸
透性がよいためパッカー効果の確実な二重管ダブルパッ
カー工法を採用する場合には、注入速度を大きくして、
施工効率を上げることが出来、他方一度に注入する注入
孔が多く、その注入孔が注入管の上下広い範囲に拡がっ
ているような注入管を使用する工法(ここでは多孔注入
工法とする)では、注入速度を小さくして、地盤が隆起
することなく、浸透注入させることが出来る。Further, the ground consolidation material of the present invention has a low viscosity and a good permeability, so that when the double pipe double packer method of ensuring a packer effect is adopted, the injection speed is increased.
The construction efficiency can be improved, and on the other hand, there is a large number of injection holes to be injected at once, and a method using an injection pipe that spreads over a wide area above and below the injection pipe (here, the porous injection method) is used. In addition, the injection speed can be reduced so that the infiltration can be performed without raising the ground.
【0021】[0021]
【実施例】以下、本発明を実施例によって具体的に説明
するが、これらの実施例は本発明の一例に過ぎず、本発
明はこれらの実施例に限定されるものではない。まず、
本発明の実施例および比較例に用いた中性シリカゾル、
スラグ、セメントおよび増粘時間の調整剤を以下にまと
めて示す。 (1)中性シリカゾル 水ガラスをイオン交換樹脂で処理することによりアルカ
リの大部分を除去し、造粒して得られた、表1に示す組
成の中性シリカゾル(旭電化工業(株)製)を使用し
た。EXAMPLES Hereinafter, the present invention will be described specifically with reference to examples, but these examples are merely examples of the present invention, and the present invention is not limited to these examples. First,
Neutral silica sol used in Examples and Comparative Examples of the present invention,
The slag, cement and thickening time regulator are summarized below. (1) Neutral silica sol A neutral silica sol having the composition shown in Table 1 obtained by treating water glass with an ion-exchange resin to remove most of the alkali and granulating it (manufactured by Asahi Denka Kogyo KK) )It was used.
【0022】[0022]
【表1】 [Table 1]
【0023】(2)スラグ 表2に示す組成および粉砕度の異なる3種類のスラグを
使用した。(2) Slag Three kinds of slags having different compositions and pulverization degrees shown in Table 2 were used.
【0024】[0024]
【表2】 [Table 2]
【0025】(3)セメント 表3に示す組成および粉砕度の異なるポルトランドセメ
ントと高炉セメントを使用した。(3) Cement Portland cement and blast furnace cement having different compositions and pulverization degrees shown in Table 3 were used.
【0026】[0026]
【表3】 [Table 3]
【0027】(4)増粘時間の調整剤 代表的な増粘時間の調整剤として炭酸水素ナトリウム
(試薬1級:NaHCO3 )を使用した。(4) Thickening time regulator Sodium bicarbonate (reagent first grade: NaHCO 3 ) was used as a typical thickening time regulator.
【0028】実施例1〜9及び比較例1〜6 表1の中性シリカゾルと炭酸水素ナトリウムおよび水を
A液とし、B液として表2のスラグ、表3のセメントの
水懸濁液を用い、A液とB液を表4に示す割合で混合し
各種の地盤固結材を調製した。得られた地盤固結材につ
いてB型粘度計により増粘時間を測定し、また土質工学
会基準「土の一軸圧縮試験方法」に準じて一軸圧縮強度
を測定した。実施例1〜9の配合は、いずれも増粘後1
0分以上可塑状態が続いた。結果を表4に示す。Examples 1 to 9 and Comparative Examples 1 to 6 The neutral silica sol, sodium bicarbonate and water in Table 1 were used as the liquid A, and the slag shown in Table 2 and the aqueous suspension of the cement shown in Table 3 were used as the liquid B. , A liquid and B liquid were mixed at the ratios shown in Table 4 to prepare various types of ground consolidated materials. The thickening time of the obtained ground consolidation material was measured by a B-type viscometer, and the uniaxial compressive strength was measured in accordance with the Japan Society of Soil Engineering Standard “Uniaxial compression test method for soil”. The compositions of Examples 1 to 9 were all 1 after thickening.
The plastic state continued for 0 minutes or more. Table 4 shows the results.
【0029】[0029]
【表4】 [Table 4]
【0030】・注1 3時間経過後も殆ど増粘しなかっ
た。* 1 After 3 hours, the viscosity hardly increased.
【0031】・注2 3時間経過後も500cpsに達しなか
った。* 2 Even after 3 hours, it did not reach 500 cps.
【0032】・増粘時間は液温20℃で測定した。The thickening time was measured at a liquid temperature of 20 ° C.
【0033】実施例10〜12及び比較例7、8 上記実施例及び比較例の幾つかの配合について浸透試験
を行った。その結果を表5に示す。Examples 10 to 12 and Comparative Examples 7 and 8 A penetration test was carried out for some of the formulations of the above Examples and Comparative Examples. Table 5 shows the results.
【0034】<浸透試験>5φ×100cmのアクリル
パイプに豊浦標準砂を相対密度約60%となるように充
填し、水で飽和させた後、上記代表的な実施例および比
較例の配合液を注入圧1kgf/cm2 で注入し浸透距離を測
定した。豊浦標準砂の充填は所定量を数回に分けて行
い、その都度パイプの側面をハンマーで叩いた。また配
合液の調製はミキサーにA,B両液を入れ10秒間攪拌
により行った。なお浸透距離はパイプの外部から目視に
より明確に色の変化のある範囲を測定し浸透距離とし
た。<Infiltration test> A 5φ x 100cm acrylic pipe was filled with Toyoura standard sand so as to have a relative density of about 60%, saturated with water, and then mixed with the above-mentioned typical examples and comparative examples. It was injected at an injection pressure of 1 kgf / cm 2 and the permeation distance was measured. The filling of Toyoura standard sand was performed by dividing a predetermined amount into several times, and each time the side of the pipe was hit with a hammer. Further, the preparation of the compounding liquid was carried out by putting both liquids A and B in a mixer and stirring for 10 seconds. The permeation distance was defined as a permeation distance by measuring a range where the color was clearly changed from outside the pipe by visual observation.
【0035】[0035]
【表5】 [Table 5]
【0036】・*比較例7は増粘が早いため、浸透距離
が短くなったものと思われる。* In Comparative Example 7, it is considered that the permeation distance was shortened because the viscosity increased quickly.
【0037】実施例13〜16及び比較例9、10 上記実施例および比較例の幾つかの配合について30℃
における増粘時間を測定した。なお増粘時間の調整剤
(炭酸水素ナトリウム)の使用量は表6のように追加
し、他の量は同じとした。その結果を表6に示す。この
結果より、高温においても増粘時間が長く、十分浸透可
能であることが分かる。なお、可塑状態は比較例を除い
て、実施例のものはいずれも30分以上であった。Examples 13 to 16 and Comparative Examples 9 and 10 30 ° C. for some formulations of the above Examples and Comparative Examples
Was measured for the thickening time. The amount of the thickening time regulator (sodium bicarbonate) used was added as shown in Table 6, and the other amounts were the same. Table 6 shows the results. From this result, it can be seen that the thickening time is long even at a high temperature, and the resin can be sufficiently penetrated. Except for the comparative example, the plastic state of each of the examples was 30 minutes or more.
【0038】[0038]
【表6】 [Table 6]
【0039】・*のついているものはゲル化時間(カッ
プ倒立法による)である。The one marked with * is the gel time (by the inverted cup method).
【0040】実施例17、18及び比較例11、12 上記実施例および比較例の幾つかの配合について土中ゲ
ル化時間、増粘時間(またはゲル化時間)を測定した。
その結果を表7に示す。 <土中ゲル化時間測定法>ミキサーで10秒間攪拌混合
して配合液を調製し、その中から50gを直ちに豊浦標
準砂100gに添加混合し静置した。そこへ竹串を刺
し、引き抜いた時に串の跡が残るように成った時間を測
定し、土中ゲル化時間とした。なお同時に残った配合液
で増粘時間(比較例の場合はゲル化時間)を測定した。Examples 17 and 18 and Comparative Examples 11 and 12 The gelling time in soil and the thickening time (or gelling time) were measured for some formulations of the above Examples and Comparative Examples.
Table 7 shows the results. <Measurement method for gelation time in soil> A mixing liquid was prepared by stirring and mixing with a mixer for 10 seconds, and 50 g of the mixture was immediately added to 100 g of Toyoura standard sand, mixed and allowed to stand. The bamboo skewer was stabbed there, and the time at which the skewer mark was left when the bamboo skewer was pulled out was measured, and the time was taken as the soil gelation time. At the same time, the thickening time (gelation time in the case of the comparative example) was measured for the remaining mixture.
【0041】[0041]
【表7】 [Table 7]
【0042】・比較例の場合(*印)はゲル化時間であ
る。In the case of the comparative example (marked with *), the gelation time is shown.
【0043】[0043]
【発明の効果】本発明は以上の通りであり、中性シリカ
ゾルと微粒子セメント(及び必要に応じて微粒子スラ
グ)とを有効成分とする地盤固結材は、特定量の中性シ
リカゾルを使用することにより以下のような効果を発揮
する。The present invention is as described above, and a specific amount of neutral silica sol is used as a ground consolidation material containing neutral silica sol and fine particle cement (and fine particle slag as necessary) as active ingredients. Thereby, the following effects are exhibited.
【0044】中性シリカゾルを少量添加したことによ
り微粒子セメント(および微粒子スラグ)の注入時の土
粒子間での目詰まりを低減させることが出来るため、地
盤への浸透性が極めて優れている。 比較的長い注入可能時間とすることが出来るため、1
液配合として注入することも出来る。 溶液型では見られない高い固結強度が得られる。 中性シリカゾルは通常の水ガラスのように高アルカリ
成分を多量には含有していないため、アルカリの溶脱に
よる環境への影響が少ない。 セメントを比較的多く使用した場合でも、中性シリカ
ゾルは通常の水ガラスのような高アルカリ成分を殆ど含
有していないため、固結物は耐久性がある。セメントの
カルシウム成分はアルカリにより水に溶解しやすくなる
が、中性のシリカゾルを使用しているために、これと反
応して水に溶解しにくい化合物(カルシウムシリケート
類)になるため、固結物は耐久性が良好となるのであ
る。 止水効果が大きいために、掘削するような工事に対し
ても単独で目的を達することができる。 浸透性が良好であるため、注入による地盤隆起がな
い。By adding a small amount of neutral silica sol, it is possible to reduce clogging between the soil particles at the time of injecting the fine cement (and the fine slag), so that the permeability to the ground is extremely excellent. Since the injection time can be relatively long, 1
It can also be injected as a liquid formulation. High consolidation strength not found in solution type is obtained. Neutral silica sol does not contain a large amount of a high alkali component unlike ordinary water glass, so that the leaching of alkali has little effect on the environment. Even when a relatively large amount of cement is used, the consolidated silica is durable because the neutral silica sol hardly contains a high alkali component such as ordinary water glass. The calcium component of cement is easily dissolved in water due to alkali, but because it uses neutral silica sol, it reacts with it to become a compound (calcium silicates) that is difficult to dissolve in water. Has good durability. Since the water stopping effect is large, it can achieve its purpose independently even for excavation work. There is no ground uplift due to injection due to good permeability.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C09K 17/10 C09K 17/10 P E02D 3/12 101 E02D 3/12 101 //(C04B 28/02 (C04B 28/02 22:06 22:06 A 22:10 22:10 18:14 18:14 A ) ) F 103:44 103:44 111:70 111:70 C09K 103:00 C09K 103:00 (72)発明者 島田 俊介 東京都文京区本郷2丁目15番10号 強化土 エンジニヤリング株式会社内 Fターム(参考) 2D040 AA01 AB01 CA01 CA02 CA04 CB03 CC01 4G012 PA29 PB04 PB08 PC08 4H026 CA03 CB02 CB03 CB07 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C09K 17/10 C09K 17/10 P E02D 3/12 101 E02D 3/12 101 // (C04B 28/02 ( C04B 28/02 22:06 22:06 A 22:10 22:10 18:14 18:14 A)) F 103: 44 103: 44 111: 70 111: 70 C09K 103: 00 C09K 103: 00 (72) Inventor Shunsuke Shimada 2-15-10, Hongo, Bunkyo-ku, Tokyo F-term (in reference) 2D040 AA01 AB01 CA01 CA02 CA04 CB03 CC01 4G012 PA29 PB04 PB08 PC08 4H026 CA03 CB02 CB03 CB07
Claims (4)
換樹脂で除去し、造粒して得られた中性シリカゾルと、
微粒子セメントと、必要に応じて用いられるスラグとを
有効成分とする地盤固結材であって、中性シリカゾルの
含有量が、SiO2 濃度30%のシリカゾル換算で全配
合液中、0.5〜5容量%である地盤固結材。A neutral silica sol obtained by removing most of the alkali of water glass with an ion exchange resin and granulating the water glass,
A ground consolidating material containing fine particle cement and slag used as required as active ingredients, wherein the content of neutral silica sol is 0.5% in the total formulation liquid in terms of silica sol with a SiO 2 concentration of 30%. Ground consolidation material that is ~ 5% by volume.
びスラグの使用量が、次の要件(1)および(2)のい
ずれかを具備してなる請求項1記載の地盤固結材。 (1)微粒子セメント単独の場合には、微粒子セメント
の配合量が、全配合液1,000mlあたり30〜300
gであること (2)微粒子セメントとスラグを使用する場合には、そ
れらの重量割合が、微粒子セメント:スラグ=100〜
20:0〜80であること2. The ground consolidating material according to claim 1, wherein the amount of the fine cement and the slag used satisfies one of the following requirements (1) and (2). (1) When the fine particle cement is used alone, the compounding amount of the fine particle cement is 30 to 300 per 1,000 ml of the total liquid mixture.
(2) When fine particle cement and slag are used, their weight ratio is fine particle cement: slag = 100 to
20: 0 to 80
表面積4,000cm2/g 以上である請求項1記載の地盤
固結材。3. The soil consolidation material according to claim 1, wherein the fine particle cement has a specific surface area of 4,000 cm 2 / g or more.
剤を含有し、有効成分の使用量が以下の(3)及び
(4)を満足する範囲であり、配合液が単独でゲル状態
になった時の強度が0.1kgf/cm2 以下である請求項1
記載の地盤固結材。 (3)微粒子セメントの使用量が、配合液1,000ml
あたり30〜300gであること (4)増粘時間の調整剤の使用量が、微粒子セメントに
対し0.1〜10重量%であること4. The composition according to claim 1, further comprising a thickening time regulator, wherein the amount of the active ingredient used is within the range satisfying the following (3) and (4), and the compounded liquid alone is in a gel state. The strength at the time of becoming 1 kgf / cm 2 or less.
The ground consolidation material described. (3) The amount of particulate cement used is 1,000 ml
(4) The amount of the thickening time modifier used is 0.1 to 10% by weight based on the fine particle cement.
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JP27647399A JP3721289B2 (en) | 1999-09-29 | 1999-09-29 | Ground consolidation material |
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JP27647399A JP3721289B2 (en) | 1999-09-29 | 1999-09-29 | Ground consolidation material |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006129884A1 (en) * | 2005-06-02 | 2006-12-07 | Kyokado Engineering Co., Ltd. | Plastic gel grout and method of ground reinforcement |
JP2007314724A (en) * | 2006-05-29 | 2007-12-06 | Raito Kogyo Co Ltd | Material for soil improvement |
JP2013193899A (en) * | 2012-03-16 | 2013-09-30 | Nihon Univ | Hardening accelerator and curing method of hydraulic material |
JP2021127446A (en) * | 2020-02-14 | 2021-09-02 | 花王株式会社 | Ground improvement method |
JP7308499B1 (en) | 2022-09-06 | 2023-07-14 | 強化土エンジニヤリング株式会社 | Ground consolidation material and ground grouting method using it |
-
1999
- 1999-09-29 JP JP27647399A patent/JP3721289B2/en not_active Expired - Fee Related
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006129884A1 (en) * | 2005-06-02 | 2006-12-07 | Kyokado Engineering Co., Ltd. | Plastic gel grout and method of ground reinforcement |
US8596924B2 (en) | 2005-06-02 | 2013-12-03 | Kyokado Engineering Co., Ltd. | Method for strengthening a ground |
JP2007314724A (en) * | 2006-05-29 | 2007-12-06 | Raito Kogyo Co Ltd | Material for soil improvement |
JP2013193899A (en) * | 2012-03-16 | 2013-09-30 | Nihon Univ | Hardening accelerator and curing method of hydraulic material |
JP2021127446A (en) * | 2020-02-14 | 2021-09-02 | 花王株式会社 | Ground improvement method |
JP7299869B2 (en) | 2020-02-14 | 2023-06-28 | 花王株式会社 | Ground improvement method |
JP7308499B1 (en) | 2022-09-06 | 2023-07-14 | 強化土エンジニヤリング株式会社 | Ground consolidation material and ground grouting method using it |
JP2024037096A (en) * | 2022-09-06 | 2024-03-18 | 強化土エンジニヤリング株式会社 | Soil solidification material and ground injection method using the same |
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