JPH0559363A - Hydrous soil improver - Google Patents
Hydrous soil improverInfo
- Publication number
- JPH0559363A JPH0559363A JP22008291A JP22008291A JPH0559363A JP H0559363 A JPH0559363 A JP H0559363A JP 22008291 A JP22008291 A JP 22008291A JP 22008291 A JP22008291 A JP 22008291A JP H0559363 A JPH0559363 A JP H0559363A
- Authority
- JP
- Japan
- Prior art keywords
- water
- soil
- fly ash
- present
- weight
- 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
- 239000002689 soil Substances 0.000 title claims abstract description 50
- 239000010881 fly ash Substances 0.000 claims abstract description 26
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 15
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims abstract description 9
- 235000011941 Tilia x europaea Nutrition 0.000 claims abstract description 9
- 229910052602 gypsum Inorganic materials 0.000 claims abstract description 9
- 239000010440 gypsum Substances 0.000 claims abstract description 9
- 239000004571 lime Substances 0.000 claims abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 40
- 238000010276 construction Methods 0.000 abstract description 7
- 230000000694 effects Effects 0.000 abstract description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 18
- 238000000034 method Methods 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 10
- 239000000292 calcium oxide Substances 0.000 description 9
- 235000012255 calcium oxide Nutrition 0.000 description 9
- 150000003839 salts Chemical group 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- -1 alkali metal salts Chemical class 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 239000004576 sand Substances 0.000 description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000004568 cement Substances 0.000 description 4
- 230000007613 environmental effect Effects 0.000 description 4
- 229920002401 polyacrylamide Polymers 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 239000007870 radical polymerization initiator Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- NDAJNMAAXXIADY-UHFFFAOYSA-N 2-methylpropanimidamide Chemical compound CC(C)C(N)=N NDAJNMAAXXIADY-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000010883 coal ash Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000012024 dehydrating agents Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 238000000643 oven drying Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 239000003516 soil conditioner Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
Abstract
(57)【要約】
【構成】 フライアッシュ、石灰および/または石
コウ、および水溶性重合体、とから成る含水土壌の改
良剤。
【効果】 高含水比の建設残土の土質を改良し、これを
埋め戻し等で再利用することができる。フライアッシュ
の再利用にもなる。(57) [Summary] [Structure] A hydrated soil improver comprising fly ash, lime and / or gypsum, and a water-soluble polymer. [Effect] The soil quality of construction residual soil with a high water content can be improved and reused for backfilling. It can also be used as fly ash.
Description
【0001】[0001]
【産業上の利用分野】本発明は、含水土壌の改良剤に関
し、特に建設および土木工事等に伴って発生する建設残
土など(以下、残土という)を土質改良し、資源として
再利用を図るのに適した含水土壌の改良剤に関するもの
である。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an agent for improving water-containing soil, and in particular, it improves soil quality of construction residual soil (hereinafter referred to as "remaining soil") generated by construction and civil engineering work and reuses it as a resource. The present invention relates to a water-containing soil improving agent suitable for.
【0002】[0002]
【従来の技術】従来、各地で発生した残土の殆どは再利
用できず埋立て処分したり他の場所へ搬出したりしてい
るが、かなりの不法投棄があり、環境破壊の問題として
重要性が増してきている。これは残土の発生量が、活発
な再開発事業などで急増傾向にある半面、海面埋立て工
事が減少傾向で有るため、残土受入場所の確保が難しく
なってきていることに起因している。2. Description of the Related Art Conventionally, most of the remaining soil generated in various places cannot be reused and is either disposed of in landfill or taken out to other places, but there is considerable illegal dumping, which is an important issue for environmental destruction. Is increasing. This is because the amount of residual soil is increasing rapidly due to active redevelopment projects, while land reclamation work is decreasing, making it difficult to secure a place for receiving residual soil.
【0003】また、道路工事の場合には、堀り起こした
現場の埋め戻しに、法律上、砂を用いることと定められ
ている。従って、埋め戻しには一般に他の場所より山砂
を持ってこなければならず、こちらでも環境破壊の問題
が起こりつつある。このような情勢の中で発生した残土
の再利用に関して、生石灰を用いた残土処理のテストプ
ラントを稼働させている例がある。In the case of road construction, it is legally required to use sand to backfill the dug up site. Therefore, in general, it is necessary to bring the sand and sand to the backfill from other places, and the problem of environmental destruction is also occurring here. Regarding the reuse of the residual soil generated in such a situation, there is an example of operating a test plant for the residual soil treatment using quicklime.
【0004】一方、国内の石炭火力発電所で発生する石
炭灰「フライアッシュ」の発生量は、1990年で推定
500万トンある。その利用法は長年検討されている
が、わずかにフライアッシュセメントの原料として用い
られているに過ぎず、大部分は海面埋立てなどの際に廃
棄処分されている。しかしながら、その処理量が莫大な
ため、海洋における環境問題等が懸念されている。On the other hand, the amount of coal ash "fly ash" generated in domestic coal-fired power plants is estimated at 5 million tons in 1990. Although its usage has been studied for many years, it is only used as a raw material for fly ash cement, and most of it is disposed of at the time of sea landfill. However, since the amount of processing is huge, there are concerns about environmental problems in the ocean.
【0005】[0005]
【発明が解決しようとする課題】前記テストプラントの
方法は、良質な残土のみを対象とし、敷地が広大なため
天日乾燥し含水比の低い残土を対象に改良しているもの
である。一方、通常の改良プラントを考える場合は敷地
が広く取れないので、現場で発生した含水比の高い残土
を天日乾燥せずにそのまま改良しなければならず、この
ような含水比の高い土は粘着性が大であり、混合機など
に付着して操業が難しく処理できない。また、処理して
も土の強度の向上が望めないなどの問題があった。The method of the test plant described above is intended to improve only the residual soil of good quality, and is intended for the residual soil that is sun-dried and has a low water content because the site is vast. On the other hand, when considering an ordinary improvement plant, the site cannot be large, so the residual soil with a high water content generated at the site must be improved as it is without drying in the sun. It is highly sticky and adheres to mixers, etc., making it difficult to operate and not processing. In addition, there is a problem in that the strength of soil cannot be expected to improve even if treated.
【0006】[0006]
【課題を解決するための手段】本発明者等は、従来技術
の課題を解決し、残土の再利用に関し優れた改良剤を得
るべく鋭意検討した結果、フライアッシュと特定の成分
を併用使用することにより、残土等の含水土壌を埋め戻
しに再利用できることを見出し、本発明に到達した。即
ち、本発明の要旨は、フライアッシュ、石灰および
/または石コウ、および水溶性重合体、とから成る含
水土壌の改良剤に存する。Means for Solving the Problems The inventors of the present invention have made intensive studies to solve the problems of the prior art and obtain an excellent improving agent for reusing the residual soil, and as a result, use fly ash and specific components in combination. As a result, they have found that water-containing soil such as residual soil can be reused for backfilling, and have reached the present invention. That is, the gist of the present invention lies in a hydrated soil conditioner comprising fly ash, lime and / or gypsum, and a water-soluble polymer.
【0007】以下、本発明を詳細に説明する。本発明に
おける含水土壌の改良とは、軟弱または粘着性の高い含
水土壌を埋め戻し等に再利用するため、強度の向上を図
るとともに砂の様に流動性を付与し、また水中で膨潤し
ないよう固化処理することである。従って、本発明にお
ける含水土壌の改良とは、含水土壌を単に塊状固化し、
流動性が失われた状態にするものではない。The present invention will be described in detail below. The improvement of the water-containing soil in the present invention is to reuse the water-containing soil having high softness or high stickiness for backfilling or the like, so as to improve the strength and impart fluidity like sand, and to prevent swelling in water. It is to solidify. Therefore, the improvement of the water-containing soil in the present invention simply solidifies and solidifies the water-containing soil,
It does not leave liquidity lost.
【0008】本発明に使用するフライアッシュとは、一
般的に定義されている、微粉炭燃焼ボイラーの煙導ガス
から採取されるアッシュであるが、通常、石炭火力発電
所で発生する石炭灰が用いられる。フライアッシュの組
成は、原料の石炭により多少異なるが、構成成分とし
て、通常、SiO2を50〜70重量%、Al2O3が1
0〜40重量%、その他Fe2O3、CaO、MgOなど
が含まれている。The fly ash used in the present invention is an ash which is generally defined and which is extracted from smoke-bearing gas of a pulverized coal combustion boiler. Used. The composition of fly ash varies slightly depending on the raw material coal, but the constituent components are usually 50 to 70% by weight of SiO 2 and 1 of Al 2 O 3.
0-40% by weight, and also contains Fe 2 O 3 , CaO, MgO and the like.
【0009】なお、フライアッシュの利用形態として、
ポルドランドセメントに通常10〜30重量%のフライ
アッシュを混合したフライアッシュセメントとする場合
があるが、このフライアッシュセメントも本発明のフラ
イアッシュとして使用することができる。本発明に使用
する石灰は、好ましくは、生石灰であるが消石灰を用い
ることもできる。生石灰は通常市販されているものでよ
く、また、一般の食品工業や家庭から発生した魚貝類の
骨殻、および発電所等の冷却管に付着した貝殻などを焼
いて粉砕して得た物を用いることもできる。[0009] As a form of using fly ash,
Usually, 10 to 30% by weight of fly ash is mixed with Pordland cement to prepare a fly ash cement, and this fly ash cement can also be used as the fly ash of the present invention. The lime used in the present invention is preferably quick lime, but slaked lime can also be used. The quicklime may be one that is usually sold on the market. It can also be used.
【0010】本発明に使用する石コウは、好ましくは無
水石コウであるが、半水石コウを用いることもできる。
フライアッシュと、石灰および/または石コウの重量比
は、通常1:0.01〜50、好ましくは1:0.05
〜20、更に好ましくは1:0.01〜10である。The gypsum used in the present invention is preferably anhydrous gypsum, but hemihydrate gypsum can also be used.
The weight ratio of fly ash to lime and / or gypsum is usually 1: 0.01 to 50, preferably 1: 0.05.
-20, more preferably 1: 0.01-10.
【0011】本発明に使用する水溶性重合体とは、通
常、少なくとも、100mlの水に1g以上溶解する重
合体であって、一般には、(メタ)アクリルアミドの単
独重合体またはその共重合体が例示される。該共重合体
としては、好ましくは親水性基としてカルボキシル基を
有するものであり、特に重合体を構成する全単量体のう
ち、カルボキシル基を有する単量体が、通常1〜80モ
ル%、好ましくは5〜60モル%含まれるものである。
また、カルボキシル基は、遊離酸または塩の形のどちら
で存在していてもよい。The water-soluble polymer used in the present invention is usually a polymer which is dissolved in at least 1 g or more in 100 ml of water, and is generally a (meth) acrylamide homopolymer or a copolymer thereof. It is illustrated. The copolymer preferably has a carboxyl group as a hydrophilic group, and in particular, of all monomers constituting the polymer, the monomer having a carboxyl group is usually 1 to 80 mol%, It is preferably contained in an amount of 5 to 60 mol%.
In addition, the carboxyl group may be present in either free acid or salt form.
【0012】塩の種類としては、例えばナトリウム、カ
リウムなどのアルカリ金属の塩、カルシウム、マグネシ
ウムなどのアルカリ土類金属の塩、アンモニウム塩、炭
素数1〜18のアルキルアミン、アルカノールアミンな
どのアミン塩、およびこれら2種以上の混合物がある
が、好ましくはアルカリ金属の塩である。Examples of the salt include alkali metal salts such as sodium and potassium, alkaline earth metal salts such as calcium and magnesium, ammonium salts, amine salts such as alkylamines having 1 to 18 carbon atoms and alkanolamines. , And a mixture of two or more of them, but an alkali metal salt is preferable.
【0013】かかるカルボキシル基を有する水溶性重合
体としては、(メタ)アクリル酸またはその塩を含有す
る(メタ)アクリルアミド系重合体、マレイン酸または
その塩と酢酸ビニルとの共重合体、イタコン酸またはそ
の塩と(メタ)アクリルアミドとの共重合体などがある
が、好ましくは(メタ)アクリル酸またはその塩を含有
する(メタ)アクリルアミド系重合体である。(メタ)
アクリル酸またはその塩を含有するアクリルアミド系重
合体としては、(メタ)アクリル酸またはその塩と(メ
タ)アクリルアミドを共重合したもののほか、(メタ)
アクリルアミドを部分加水分解したものでもよい。ま
た、以上示したような単量体を組合わせて共重合したも
のでもよい。As the water-soluble polymer having a carboxyl group, a (meth) acrylamide-based polymer containing (meth) acrylic acid or a salt thereof, a copolymer of maleic acid or a salt thereof with vinyl acetate, and itaconic acid. Further, there are copolymers of salts thereof with (meth) acrylamide, etc., but (meth) acrylamide polymers containing (meth) acrylic acid or salts thereof are preferable. (Meta)
Examples of the acrylamide polymer containing acrylic acid or a salt thereof include those obtained by copolymerizing (meth) acrylic acid or a salt thereof with (meth) acrylamide, and (meth)
It may be a partially hydrolyzed product of acrylamide. Further, a copolymer obtained by combining the above-mentioned monomers may be used.
【0014】更に、上記の重合体には、親水性基として
スルホン酸基を含む単量体、例えばビニルスルホン酸、
アリルスルホン酸、2−アクリルアミド−2−メチルプ
ロパンスルホン酸及びこれらの塩などを含めて共重合し
たものでもよい。また、水溶性を阻害しない程度の量で
あれば、オレフィン、アクリル酸エステル、ビニルエス
テルのような疎水性単量体を含んでいてもよい。Further, in the above polymer, a monomer containing a sulfonic acid group as a hydrophilic group, such as vinyl sulfonic acid,
It may be a copolymer including allyl sulfonic acid, 2-acrylamido-2-methylpropane sulfonic acid and salts thereof. Further, a hydrophobic monomer such as an olefin, an acrylic ester, or a vinyl ester may be contained as long as it does not impair the water solubility.
【0015】本発明で使用される水溶性重合体の分子量
は、通常100万以上、好ましくは500万以上であ
る。製法は特に限定されないが、一般にラジカル重合法
であり、水または低級アルコールなどを溶媒とした溶液
重合が採用される。単量体の濃度は通常10重量%以
上、好ましくは15〜60重量%である。The molecular weight of the water-soluble polymer used in the present invention is usually 1,000,000 or more, preferably 5,000,000 or more. Although the production method is not particularly limited, it is generally a radical polymerization method, and solution polymerization using water or a lower alcohol as a solvent is adopted. The concentration of the monomer is usually 10% by weight or more, preferably 15 to 60% by weight.
【0016】重合開始剤は水溶媒で重合する場合、過硫
酸カリウム、過硫酸アンモニウムなどの過酸化物、およ
びそれらを用いたレドックス系開始剤、N、N’−アゾ
ビス−(2−アミジノプロパン)・2塩酸塩、4、4’
−アゾビス−(4−シアノ吉草酸)−2−ナトリウムな
どの水溶性ラジカル重合開始剤が好ましい。ラジカル重
合開始剤の使用量は、共重合可能な単量体の混合物の重
量に対して通常0.005〜5重量%、好ましくは0.
05〜0.5重量%である。When a polymerization initiator is polymerized in an aqueous solvent, peroxides such as potassium persulfate and ammonium persulfate, and redox type initiators using them, N, N'-azobis- (2-amidinopropane). Dihydrochloride, 4,4 '
A water-soluble radical polymerization initiator such as -azobis- (4-cyanovaleric acid) -2-sodium is preferable. The amount of the radical polymerization initiator used is usually 0.005 to 5% by weight, preferably 0.1% to the weight of the copolymerizable monomer mixture.
It is from 05 to 0.5% by weight.
【0017】重合方法は、特に制限されないが、水溶液
重合を例示するならば、撹拌下重合する方法、容器中で
静置し断熱状態で重合する方法、シート状で除熱しつつ
重合する方法、油中水型エマルジョンまたは分散状態で
重合する方法が例示される。静置して重合する方法とし
ては、所定の単量体水溶液に窒素ガスを通じて酸素を除
いた後、所定温度となしラジカル重合開始剤を添加し均
一に混合後、窒素ガス気流化、所定温度に保持する方法
が例示される。重合温度は、通常10〜150°Cの範
囲で目的の重合物の分子量に応じて選択されるが、好ま
しくは40〜80°Cである。The polymerization method is not particularly limited, but if an aqueous solution polymerization is exemplified, a method of polymerization with stirring, a method of polymerization in an adiabatic state by standing in a container, a method of polymerization while removing heat in a sheet form, an oil A method of polymerizing in a water-in-water emulsion or dispersion state is exemplified. As a method of standing and polymerizing, after removing oxygen through a predetermined monomer aqueous solution through nitrogen gas, a predetermined temperature and no radical polymerization initiator are added and uniformly mixed, and then a nitrogen gas stream is generated and a predetermined temperature is set. A holding method is exemplified. The polymerization temperature is usually selected in the range of 10 to 150 ° C according to the molecular weight of the desired polymer, but is preferably 40 to 80 ° C.
【0018】かくして得られた重合体はそのまま乾燥器
で乾燥、または脱水剤で処理した後、乾燥し粉砕して試
料に供される。水溶性重合体と石灰または石コウの混合
重量比は、通常1:1〜1:500、好ましくは1:2
〜1:250である。The polymer thus obtained is directly dried in a drier or treated with a dehydrating agent, dried and pulverized before being used as a sample. The mixing weight ratio of the water-soluble polymer and lime or gypsum is usually 1: 1 to 1: 500, preferably 1: 2.
˜1: 250.
【0019】本発明の対象となる土壌は、通常、含水比
20以上の土壌である。特に本発明の改良剤の使用が期
待できるのは、含水比40〜200%、更には含水比5
0〜150%程度の含水比の高い土壌であり、具体的に
は上下水道工事、道路工事、宅地造成工事など一般の土
木・建設工事にともなって発生する残土である。尚、含
水比とは、110°Cの炉乾燥によって失われる土中水
の質量の、土の炉乾燥質量に対する比を百分率で表した
値であり、JISA1203(含水比試験方法)によっ
て測定される値である。The soil to which the present invention is applied is usually a soil having a water content ratio of 20 or more. In particular, the use of the improving agent of the present invention can be expected to have a water content ratio of 40 to 200%, and further a water content ratio of 5%.
It is a soil with a high water content ratio of 0 to 150%, and specifically, it is the residual soil that is generated by general civil engineering and construction work such as water and sewer construction, road construction, and residential land development. The water content ratio is a value representing the ratio of the mass of soil water lost by oven drying at 110 ° C to the oven dry mass of soil in percentage, and is measured by JISA1203 (water content test method). It is a value.
【0020】土質には関東ローム層、砂礫、土砂などが
あり、通常はこれらの混合物であるが、発生現場によっ
てはコンクリート片などが混入している場合もある。含
水比は土質により異なるため、発生する現場によるとこ
ろが大きい。含水比の高いものには例えば関東ローム層
があり、通常80〜120%前後の含水比を示し、粘着
性が大きいが、本発明の改良剤を使用することにより固
化および造粒されるため流動性が付与され、粘着性およ
び水中での膨潤性が無くなり、地盤支持力が向上し埋め
戻し再利用可能とすることができる。The soil includes the Kanto loam layer, gravel, sand and the like, which is usually a mixture of these, but concrete fragments may be mixed depending on the site of occurrence. Since the water content depends on the soil type, it depends largely on the site where the water is generated. The one having a high water content ratio is, for example, the Kanto loam layer, which usually has a water content ratio of about 80 to 120% and has a high tackiness, but it is solidified and granulated by using the improving agent of the present invention so that it is fluidized. Property is imparted, the adhesiveness and the swelling property in water are eliminated, and the ground supporting force is improved, and the backfilling can be reused.
【0021】本発明の改良剤の添加量は、被処理土壌の
含水比により異なるため特に限定されないが、石灰およ
び/または石コウの添加量は、残土に対して0.2〜2
0重量%、好ましくは0.5〜10重量%であり、フラ
イアッシュの添加量は、通常0.5〜50重量%、好ま
しくは1〜30重量%の範囲である。また、水溶性重合
体は残土に対して0.001〜1重量%、好ましくは
0.01〜0.5重量%である。The addition amount of the improving agent of the present invention is not particularly limited because it depends on the water content of the treated soil, but the addition amount of lime and / or gypsum is 0.2 to 2 with respect to the remaining soil.
It is 0% by weight, preferably 0.5 to 10% by weight, and the amount of fly ash added is usually 0.5 to 50% by weight, preferably 1 to 30% by weight. The water-soluble polymer content is 0.001 to 1% by weight, preferably 0.01 to 0.5% by weight, based on the residual soil.
【0022】本発明の改良剤の添加方法は特に限定され
ないが、好ましくは水溶性重合体およびフライアッシュ
を添加混合後に石灰および/または石コウを添加する方
法であるが、同時に添加混合またはプレミックスして使
用しても何等差しつかえない。また、土壌との混合は通
常の方法、例えばベルトコンベヤ上の含水土壌に改良剤
を散布し、バックホウにより混合する方法などが用いら
れる。フライアッシュ、石灰、石コウは、通常いずれも
粉末のまま添加されるが、水溶性重合体は粉末状の他、
水溶液として添加してもよい。The method of adding the improver of the present invention is not particularly limited, but preferably a method of adding lime and / or gypsum after adding and mixing the water-soluble polymer and fly ash, but adding and mixing or premixing at the same time. There is nothing wrong with using it. The mixing with the soil is carried out by an ordinary method, for example, a method of spraying the improving agent on the water-containing soil on a belt conveyor and mixing with a backhoe. Fly ash, lime, gypsum are usually added as powder, but the water-soluble polymer is in powder form,
You may add as an aqueous solution.
【0023】[0023]
【実施例】以下、本発明を実施例により更に具体的に説
明するが、本発明はその要旨を超えない限り、以下の実
施例に限定されるものではない。 実施例1〜3および比較例1〜9 含水土壌の内で処理の困難な、含水比80%の関東ロー
ム層を原料土として用い、改良試験を行なった。また、
フライアッシュとしては、三菱化成(株)四日市工場の
石炭火力発電設備より得られたものであり、その組成
は、SiO2が59%、Al2O3が30%、Fe2O3が
5%であった。更に、水溶性重合体として、アクリルア
ミド:アクリル酸ナトリウム=80:20(モル比)の
共重合体(極限粘度[η]=23.2)を用いた。EXAMPLES The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to the following examples unless it exceeds the gist thereof. Examples 1 to 3 and Comparative Examples 1 to 9 Using the Kanto loam layer having a water content ratio of 80%, which is difficult to treat among the water-containing soils, as a raw material soil, an improvement test was conducted. Also,
The fly ash was obtained from a coal-fired power plant at the Yokkaichi Plant of Mitsubishi Kasei Co., Ltd., and its composition was 59% SiO 2 , 30% Al 2 O 3 , and 5% Fe 2 O 3. Met. Further, as a water-soluble polymer, a copolymer of acrylamide: sodium acrylate = 80: 20 (molar ratio) (intrinsic viscosity [η] = 23.2) was used.
【0024】原料土を7kgずつポリエチレン袋に小分
けし、改良処理を行なった。改良処理は、各袋中に水溶
性重合体粉末を7gずつ降り掛けながら混合した後、フ
ライアッシュを420g(土に対して6%)、630g
(9%)、1,400g(20%)夫々混合し、更に2
10gの生石灰の粉末を加えてかき混ぜた。更に水分が
飛ばないよう直ちに密封した。6日間密閉養生後、JI
SA1210(突き固めによる土の締め固め試験方法)
に従い、内径15cmのモールドに改良土を3層に分け
て、夫々4.5kgのランマーで92回突き固めて、突
き固め試験を行なった。The raw material soil was subdivided into polyethylene bags of 7 kg each and subjected to an improvement treatment. The improvement treatment is as follows: Mix 7g of water-soluble polymer powder in each bag, and mix with fly ash 420g (6% of soil), 630g.
(9%) and 1,400 g (20%), respectively, and further 2
10 g of quicklime powder was added and stirred. Immediately sealed to prevent water from splashing. After 6 days of sealed curing, JI
SA1210 (Soil compaction test method by tamping)
According to the above, the improved soil was divided into three layers in a mold having an inner diameter of 15 cm, and each of them was tamped 92 times with a 4.5 kg rammer to perform a tamping test.
【0025】次に、JISA1211(CBR試験方
法)に従い、浸水膨張試験の準備を行ない、4日間水槽
に浸漬して膨張量を追跡した。更に、水槽より取り出し
て水を取除き、15分後に所定の測定を行なった後、C
BR(CaliforniaBearing Rati
o)試験器により荷重−貫入量曲線を求めた。貫入量
2.5mmに於ける荷重(以下、貫入強度と略す)を読
み取り次の式によりCBRを計算した。式中の標準荷重
はJISで定められている2.5mm貫入時の標準荷
重、1,370kgを用いた。CBR値は大きいほど強
度が高いことを示す。Next, according to JISA1211 (CBR test method), preparation for a water immersion expansion test was performed, and the expansion amount was traced by immersing in a water tank for 4 days. Further, after taking out from the water tank to remove water and performing a predetermined measurement after 15 minutes, C
BR (California Bearing Rati)
o) A load-penetration amount curve was obtained using a tester. The load at a penetration amount of 2.5 mm (hereinafter, abbreviated as penetration strength) was read and CBR was calculated by the following formula. The standard load in the formula was 1,370 kg, which is the standard load for 2.5 mm penetration defined by JIS. The larger the CBR value, the higher the strength.
【0026】 [0026]
【0027】また、改良土の状態を目視観察した。以上
の試験の結果を表1に示す(表中のFAはフライアッシ
ュを示す)。また、同時に測定した水浸4日後の膨張量
より求めた膨張比はいずれも1%以下で良好であった。Further, the condition of the improved soil was visually observed. The results of the above tests are shown in Table 1 (FA in the table indicates fly ash). In addition, the expansion ratios determined from the expansion amounts after 4 days of water immersion measured at the same time were all good at 1% or less.
【0028】比較例1〜3はフライアッシュと生石灰の
み併用使用した場合、比較例4は生石灰を単独使用した
場合、比較例5、6は生石灰と水溶性重合体のみ併用使
用した場合、また、比較例7、8はフライアッシュ単独
使用した場合である。更に、比較例9は原料土の試験結
果であり、粘着性が大きく突き固め試験機に掛からなか
ったので手で突き固めたものである。Comparative Examples 1 to 3 use fly ash and quick lime alone, Comparative Example 4 use quick lime alone, Comparative Examples 5 and 6 use quick lime and water-soluble polymer in combination, and Comparative Examples 7 and 8 are the cases where fly ash was used alone. Further, Comparative Example 9 is the result of the test of the raw material soil, and it was tamped by hand because it had a large tackiness and could not be tampered with by the tamping tester.
【0029】[0029]
【表1】 [Table 1]
【0030】実施例4、5および比較例10〜12 生石灰の代りに無水石コウの粉末を使う以外は、実施例
1と同様に処理して、試験を行なった。結果を表2に示
す。比較例10、11は、フライアッシュと無水石コウ
のみ併用使用した場合、比較例12は無水石コウを単独
使用した場合、更に、比較例13は無水石コウと水溶性
重合体のみ併用使用した場合である。なお、ここでの水
溶性重合体はポリアクリルアミドの30モル%部分加水
分解物(極限粘土[η]=19.5)である。Examples 4 and 5 and Comparative Examples 10 to 12 The same treatments and tests as in Example 1 were carried out except that anhydrous gypsum powder was used instead of quicklime. The results are shown in Table 2. In Comparative Examples 10 and 11, when fly ash and anhydrous gypsum were used together, Comparative Example 12 was used alone, and in Comparative Example 13, anhydrous gypsum and water-soluble polymer were used together. This is the case. The water-soluble polymer here is a 30 mol% partial hydrolyzate of polyacrylamide (extreme clay [η] = 19.5).
【0031】[0031]
【表2】 [Table 2]
【0032】[0032]
【発明の効果】従来、利用困難で不法投棄の対象となっ
ていた高含水比の残土が、本発明の含水土壌の改良剤を
用いることにより、そのまま天日乾燥せずにプラントで
改良可能となり、資源としてそのまま埋め戻し等に再利
用することができるのみなあらず、現在、処理に困って
いるフライアッシュも資源として利用できる。かくして
残土の不法投棄や、埋め戻し用砂などの採取による環境
破壊を防止するとともに、フライアッシュの海面埋立て
による環境汚染も減少できるため、地域社会に貢献する
ことが大である。EFFECTS OF THE INVENTION The residual soil having a high water content ratio, which has been conventionally difficult to use and has been subject to illegal dumping, can be improved in a plant without being directly dried in the sun by using the water-containing soil improving agent of the present invention. The fly ash, which is currently in trouble, cannot be reused as a resource for backfilling, and can be used as a resource. In this way, it is possible to prevent the environmental destruction due to illegal dumping of the residual soil and the extraction of sand for backfilling, and to reduce the environmental pollution due to the landfill of fly ash, which greatly contributes to the local community.
Claims (1)
たは石コウ、および水溶性重合体、とから成る含水土
壌の改良剤。1. A hydrated soil improver comprising fly ash, lime and / or gypsum, and a water-soluble polymer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22008291A JP3243804B2 (en) | 1991-08-30 | 1991-08-30 | Aqueous soil conditioner |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22008291A JP3243804B2 (en) | 1991-08-30 | 1991-08-30 | Aqueous soil conditioner |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0559363A true JPH0559363A (en) | 1993-03-09 |
| JP3243804B2 JP3243804B2 (en) | 2002-01-07 |
Family
ID=16745651
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22008291A Expired - Lifetime JP3243804B2 (en) | 1991-08-30 | 1991-08-30 | Aqueous soil conditioner |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3243804B2 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10147781A (en) * | 1996-11-20 | 1998-06-02 | Matsuoka Kosan Kk | Dry solidification method of mud, solidified material and dry solidified material of mud |
| US5769936A (en) * | 1995-01-09 | 1998-06-23 | Mitsubishi Chemical Corporation | Method for producing fly ash granules |
| JP2004099870A (en) * | 2002-07-16 | 2004-04-02 | Chugoku Electric Power Co Inc:The | Soil improvement material and soil improvement method |
| JP2005187620A (en) * | 2003-12-25 | 2005-07-14 | Toa Harbor Works Co Ltd | Solidifying material composition |
| JP2010030838A (en) * | 2008-07-29 | 2010-02-12 | Hiroshima Univ | Oxygen generating material, method for producing the same and environment improvement method |
| KR101363322B1 (en) * | 2011-12-27 | 2014-02-14 | 박상규 | Soil conditioner. |
-
1991
- 1991-08-30 JP JP22008291A patent/JP3243804B2/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5769936A (en) * | 1995-01-09 | 1998-06-23 | Mitsubishi Chemical Corporation | Method for producing fly ash granules |
| JPH10147781A (en) * | 1996-11-20 | 1998-06-02 | Matsuoka Kosan Kk | Dry solidification method of mud, solidified material and dry solidified material of mud |
| JP2004099870A (en) * | 2002-07-16 | 2004-04-02 | Chugoku Electric Power Co Inc:The | Soil improvement material and soil improvement method |
| JP2005187620A (en) * | 2003-12-25 | 2005-07-14 | Toa Harbor Works Co Ltd | Solidifying material composition |
| JP2010030838A (en) * | 2008-07-29 | 2010-02-12 | Hiroshima Univ | Oxygen generating material, method for producing the same and environment improvement method |
| KR101363322B1 (en) * | 2011-12-27 | 2014-02-14 | 박상규 | Soil conditioner. |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3243804B2 (en) | 2002-01-07 |
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