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JPH0249761B2 - KYUCHAKU SHORIHO - Google Patents
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JPH0249761B2 - KYUCHAKU SHORIHO - Google Patents

KYUCHAKU SHORIHO

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Publication number
JPH0249761B2
JPH0249761B2 JP4173582A JP4173582A JPH0249761B2 JP H0249761 B2 JPH0249761 B2 JP H0249761B2 JP 4173582 A JP4173582 A JP 4173582A JP 4173582 A JP4173582 A JP 4173582A JP H0249761 B2 JPH0249761 B2 JP H0249761B2
Authority
JP
Japan
Prior art keywords
titanic acid
carrageenan
water
liquid
acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP4173582A
Other languages
Japanese (ja)
Other versions
JPS58159814A (en
Inventor
Taku Tabuchi
Shoji Suzuki
Hajime Ito
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 Chemical Corp
Original Assignee
Mitsubishi Rayon Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP4173582A priority Critical patent/JPH0249761B2/en
Publication of JPS58159814A publication Critical patent/JPS58159814A/en
Publication of JPH0249761B2 publication Critical patent/JPH0249761B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Separation Of Suspended Particles By Flocculating Agents (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はチタン酸粉末を用いて液体中に含まれ
る不要物質あるいは有価物の吸着処理を行なつた
チタン酸分散液体中に酸性多糖質を加えてチタン
酸を凝集せしめることを特徴とする液体の吸着処
理方法に関する。更に詳しくは水不溶性アルミニ
ウム化合物を0.01乃至1%含有するチタン酸を吸
着処理すべき液体中に分散せしめ不要物質あるい
は有価物を吸着後、該液に酸性多糖類を0.1乃至
1%加えてチタン酸を凝集せしめることを特徴と
する液体の吸着処理方法に関するものである。 チタン酸とは含水酸化チタン又は水酸化チタン
酸とも称されるチタン化合物であり、含水の化学
的状態によりオルトチタン酸とメタチタン酸の2
種類存在するとされている。いずれのチタン酸も
両性化合物に属し吸着剤として汎く利用されてい
ることは周知のとおりである。また、このチタン
酸は海水中の微量のウランを選択的に吸着するこ
とが出来、将来、原子炉燃料は海水中からチタン
酸により回収されたウランによりまかなわれるこ
とも考えられている。 又、ウラン鉱山から廃水中には高濃度の放射性
元素であるラジウム,ウランが含まれており、該
廃水の処理にもチタン酸吸着材が使用するとその
処理効率が向上する。或いは低品位ウラン鉱山に
おいてはインプレースリーチング法により高濃度
ウラン液を得、高効率でウランを採取することが
行なわれているが、この場合にもチタン酸により
吸着回収が効率的であるとされる。 更にはチタン酸は砒素に対しても高い吸着能を
有し砒素含有廃水の処理でも有効な吸着材であ
る。 このようにチタン酸は前述した如き高い吸着能
を有するにも拘らず、その形状が粉末であるため
に取り扱いが困難であり、一般的には適当な粒径
に造粒しカラムに充填した状態で使用されてい
る。しかしながらチタン酸はその造粒により比表
面積の低下、成形剤の影響を受けるため吸着能の
低下は避けられない。 粉末状チタン酸取り扱いの問題は吸着処理のチ
タン酸の回収にある。つまり吸着処理すべき液体
中に分散したチタン酸を効率よく回収し、脱着
し、再使用するサイクルに組み込むことが出来る
ならば上述したチタン酸の造粒による不都合がな
く望しい方法であり、従来法としては、液体媒体
中に分散されたチタン酸吸着材を過法遠心分離
法等の方法によつてやつてきたがこれらの方法は
多大なエネルギーを要する。 そこで本発明者らは効率よく処理液体媒体中よ
りチタン酸を回収する方法について鋭意検討を重
ねた結果、水不溶性アルミニウム化合物を含有せ
しめた粉末状チタン酸を分散した処理水中に酸性
多糖類を添加することによりチタン酸は該媒体中
で高度に凝集せしめる本発明を完成した。これは
チタン酸中に含ませた水不溶性アルミニウム化合
物と酸性多糖類との相互作用に起因するものであ
る。 本発明を実施するに際して用いる水不溶性アル
ミニウム化合物とは酸化アルミニウム,水酸化ア
ルミニウム等実質的に水に溶解しないアルミニウ
ム含有物質を指す。本発明を実施する上で該アル
ミニウム化合物はチタン酸に0.1%以上含有せし
めれば良い。しかしこの添加量はチタン酸固有の
吸着性に影響を与えない程度の範囲にするのがよ
く、好しくは1%以下に抑制すべきである。水不
溶性アルミニウム化合物を0.1乃至1%含有せし
めたチタン酸は実質的にその吸着能力が低下しな
いだけでなく、粉末状チタン酸の要処理水中分散
性が向上することも特筆すべき点である。 かかるチタン酸を分散せしめた水中よりチタン
酸を凝集するに用いられる酸性多糖類は、寒天、
アルギン酸、カラギーナン、ペクチン、グアカ
ム、ローカストビーンガム等が挙げられる。これ
らの多糖類は水不溶性のアルミニウム化合物との
相互作用により容易に水性媒体中に於て不溶化す
る。これらの多糖類はいずれも単独で或いは2者
以上組合わせて用いることができる。とくに、常
温の水に対する溶解性もしくは膨潤性が良好であ
り、その粘度が比較的低いにもかかわらず、アル
ミニウム化合物によつて容易に凝集し、水中から
の分離回収を行いうるカラギーナン、就中イオタ
カラキーナンが有効である。カラギーナンは紅藻
類に含有されるガラクタンの硫酸エステルであり
硫酸基含有量と3.6―アンヒドロガラクトース含
有量の差によりカツパカラギーナン,ラムダカラ
ギーナン,イオタカラギーナンに大別され、この
3種のカラギーナンは物理的性質が異る。つまり
カツパカラギーナンは常温の水に難溶性であり加
温溶解後冷却により強いゲルを形成する。ラムダ
カラギーナンは常温の水に容易に溶解しゲルを形
成しない。又イオタカラギーナンは常温の水に膨
潤し加温溶解後冷却により弱いゲルを形成する。
これが一般的な性質であるが硫酸残基のカウンタ
ーイオンの種類により、特に溶解性ゲルの性質が
異る。つまりカウンターイオンとしてナトリウム
を有する場合にはカツパカラギーナン,イオタカ
ラギーナンにおいては常温の水に対する溶解性が
高くなりゲルを形成しない。 上に述べた水に対する溶解性の点より本発明の
実施に際して用いる多糖類としてはラムダカラギ
ーナン・イオタカラギーナン,及びカツパカラギ
ーナン,ナトリウム塩を用いるのが有効である。 カラギーナンの種類による物理的性質のもうひ
とつの特徴はその水溶液の粘度である。常温の水
にカラギーナンを0.5%分散せしめた時の25℃の
粘度はカツパカラギーナンは10センチポイズ
(CP),イオタカラギーナンは20CP,ラムダカラ
ギーナンは150CPである。本発明の目的を達成す
るには粘度が低い方が有効であるので、カツパカ
ラギーナン,イオタカラギーナンが良い。 カラギーナンの化学的性質として酸性下では容
易に劣化し、又酸化剤の作用によつても迅速に分
解されることが挙げられる。これらの分解は加熱
により加速される。このことは吸着回収されたチ
タン酸を酸で脱着処理した後活性化処理する際に
カラギーナンも容易に分解を受け、チタン酸の回
収が容易となるのであり、このことはチタン酸を
リサイクルして使用する上で、有利な点である。 本発明を実施するには水不溶性アルミニウム化
合物を0.01乃至1%含有せしめたチタン酸粉末を
水中に1%程度分散して処理した該分散液にカラ
ギーナンを0.1乃至1%添加撹拌した後、静置し
チタン酸の沈降せしめることによつて行なうこと
ができ、従来法に比し、その沈降速度を極めて大
きなものとすることができる。 以下実施例に従つて本発明を更に具体的に説明
する。 実施例 0.5%の酸化アルミニウムを含有するメタチタ
ン酸で320メツシユの篩を通過した粉末1部を99
部の水に加え300rpmで30分間撹拌した。 該分散液に第1表に示す酸性多糖類0.5部加え
て更に300rpmで30分間撹拌した後30分及び60分
後の沈殿層が占める体積の全体の体積に対する割
合を測定した結果を第1表に示した。
The present invention is a liquid characterized by adding an acidic polysaccharide to a titanic acid dispersion liquid which has been subjected to adsorption treatment of unnecessary substances or valuables contained in the liquid using titanic acid powder to aggregate titanic acid. This invention relates to an adsorption treatment method. More specifically, titanic acid containing 0.01 to 1% of a water-insoluble aluminum compound is dispersed in a liquid to be adsorbed, and after adsorbing unnecessary substances or valuables, 0.1 to 1% of an acidic polysaccharide is added to the liquid to absorb titanic acid. The present invention relates to a liquid adsorption treatment method characterized by agglomerating liquids. Titanic acid is a titanium compound also called hydrous titanium oxide or hydroxide titanic acid, and depending on the chemical state of water, it can be divided into two types: orthotitanic acid and metatitanic acid.
It is said that there are different types. It is well known that all titanic acids belong to amphoteric compounds and are widely used as adsorbents. Furthermore, this titanic acid can selectively adsorb trace amounts of uranium in seawater, and it is thought that in the future nuclear reactor fuel will be provided by uranium recovered from seawater using titanic acid. Furthermore, wastewater from uranium mines contains highly concentrated radioactive elements such as radium and uranium, and the use of a titanic acid adsorbent in the treatment of such wastewater improves its treatment efficiency. Alternatively, in low-grade uranium mines, high-concentration uranium liquid is obtained using an in-place leaching method and uranium is extracted with high efficiency, but in this case as well, adsorption and recovery using titanic acid is said to be efficient. Ru. Furthermore, titanic acid has a high adsorption capacity for arsenic and is an effective adsorbent for treating arsenic-containing wastewater. Although titanic acid has a high adsorption capacity as mentioned above, its powder form makes it difficult to handle, and it is generally granulated to an appropriate particle size and packed in a column. used in However, since titanic acid has a reduced specific surface area due to its granulation and is affected by the molding agent, a reduction in adsorption capacity is unavoidable. The problem with handling powdered titanic acid lies in the recovery of titanic acid through adsorption treatment. In other words, if the titanic acid dispersed in the liquid to be adsorbed can be efficiently recovered, desorbed, and incorporated into a cycle for reuse, it is a desirable method that does not have the disadvantages of titanic acid granulation as described above. As a method, a titanic acid adsorbent dispersed in a liquid medium has been used by methods such as centrifugation, but these methods require a large amount of energy. Therefore, the inventors of the present invention conducted intensive studies on a method for efficiently recovering titanic acid from a treated liquid medium, and found that an acidic polysaccharide was added to the treated water in which powdered titanic acid containing a water-insoluble aluminum compound was dispersed. By doing so, the present invention was completed in which titanic acid is highly aggregated in the medium. This is due to the interaction between the water-insoluble aluminum compound contained in titanic acid and the acidic polysaccharide. The water-insoluble aluminum compound used in carrying out the present invention refers to aluminum-containing substances that are substantially insoluble in water, such as aluminum oxide and aluminum hydroxide. In carrying out the present invention, the aluminum compound may be contained in titanic acid in an amount of 0.1% or more. However, the amount added should be within a range that does not affect the adsorption properties inherent to titanic acid, and should preferably be suppressed to 1% or less. It is noteworthy that titanic acid containing 0.1 to 1% of a water-insoluble aluminum compound not only has its adsorption capacity not substantially reduced, but also that the dispersibility of powdered titanic acid in the water required for treatment is improved. Acidic polysaccharides used to aggregate titanic acid from water in which titanic acid is dispersed include agar,
Examples include alginic acid, carrageenan, pectin, guacam, and locust bean gum. These polysaccharides are easily insolubilized in aqueous media by interaction with water-insoluble aluminum compounds. Any of these polysaccharides can be used alone or in combination of two or more. In particular, carrageenan, especially carrageenan, which has good solubility or swelling property in water at room temperature and has a relatively low viscosity, easily aggregates with aluminum compounds and can be separated and recovered from water. Takara Keenan is effective. Carrageenan is a sulfate ester of galactan contained in red algae, and is broadly classified into Katupa carrageenan, Lambda carrageenan, and Iota carrageenan depending on the difference in sulfate group content and 3.6-anhydrogalactose content.These three types of carrageenan are physically The characteristics are different. In other words, Katupa carrageenan is poorly soluble in water at room temperature, and forms a strong gel by heating and dissolving it and then cooling it. Lambda carrageenan easily dissolves in water at room temperature and does not form a gel. Furthermore, iota carrageenan swells in water at room temperature and forms a weak gel when heated and dissolved and then cooled.
Although this is a general property, the properties of the soluble gel vary depending on the type of counter ion of the sulfuric acid residue. In other words, when sodium is present as a counter ion, katsupa carrageenan and iota carrageenan have high solubility in water at room temperature and do not form gels. In view of the above-mentioned solubility in water, it is effective to use lambda carrageenan, iota carrageenan, and katsupa carrageenan, sodium salt, as the polysaccharides used in the practice of the present invention. Another physical property characteristic of carrageenan is the viscosity of its aqueous solution. When 0.5% carrageenan is dispersed in water at room temperature, the viscosity at 25°C is 10 centipoise (CP) for Katupa carrageenan, 20 CP for iota carrageenan, and 150 CP for lambda carrageenan. Since lower viscosity is more effective in achieving the object of the present invention, katsupa carrageenan and iota carrageenan are preferred. The chemical properties of carrageenan include that it easily deteriorates under acidic conditions and is also rapidly decomposed by the action of oxidizing agents. These decompositions are accelerated by heating. This means that when adsorbed and recovered titanic acid is desorbed with acid and then activated, carrageenan is easily decomposed and titanic acid can be easily recovered. This is an advantageous point in its use. To carry out the present invention, titanic acid powder containing 0.01 to 1% of a water-insoluble aluminum compound is dispersed in water at a rate of about 1%, and 0.1 to 1% of carrageenan is added to the dispersion, stirred, and allowed to stand still. This can be carried out by precipitating titanic acid, and the sedimentation rate can be made extremely high compared to conventional methods. The present invention will be described in more detail below with reference to Examples. Example: One part of powder passed through a 320 mesh sieve with metatitanic acid containing 0.5% aluminum oxide was 99%
of water and stirred at 300 rpm for 30 minutes. After adding 0.5 part of the acidic polysaccharide shown in Table 1 to the dispersion and stirring at 300 rpm for 30 minutes, Table 1 shows the results of measuring the ratio of the volume occupied by the precipitated layer to the total volume after 30 and 60 minutes. It was shown to.

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 水不溶性アルミニウム化合物を0.01乃至1%
含有せしめたチタン酸粉末を、吸着処理すべき液
体中に分散し吸着すべき物質を吸着した後該液体
に酸性多糖類を0.05乃至1%なる割合で加えてチ
タン酸粉末を凝集せしめることを特徴とする吸着
処理法。
1 0.01 to 1% water-insoluble aluminum compound
The titanic acid powder contained therein is dispersed in a liquid to be adsorbed and the substance to be adsorbed is adsorbed, and then acidic polysaccharide is added to the liquid at a ratio of 0.05 to 1% to aggregate the titanic acid powder. Adsorption treatment method.
JP4173582A 1982-03-18 1982-03-18 KYUCHAKU SHORIHO Expired - Lifetime JPH0249761B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4173582A JPH0249761B2 (en) 1982-03-18 1982-03-18 KYUCHAKU SHORIHO

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4173582A JPH0249761B2 (en) 1982-03-18 1982-03-18 KYUCHAKU SHORIHO

Publications (2)

Publication Number Publication Date
JPS58159814A JPS58159814A (en) 1983-09-22
JPH0249761B2 true JPH0249761B2 (en) 1990-10-31

Family

ID=12616674

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4173582A Expired - Lifetime JPH0249761B2 (en) 1982-03-18 1982-03-18 KYUCHAKU SHORIHO

Country Status (1)

Country Link
JP (1) JPH0249761B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8409410D0 (en) * 1984-04-11 1984-05-23 Hydro Int Ltd Water treatment
CN101579071B (en) 2009-05-18 2012-09-05 北京雷力农用化学有限公司 Method for removing arsenic from seaweed extract
JP7382552B2 (en) * 2019-05-29 2023-11-17 パナソニックIpマネジメント株式会社 Laser processing equipment and laser processing method using the same

Also Published As

Publication number Publication date
JPS58159814A (en) 1983-09-22

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