CA2212405C - Method for treating waste water - Google Patents
Method for treating waste water Download PDFInfo
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- CA2212405C CA2212405C CA002212405A CA2212405A CA2212405C CA 2212405 C CA2212405 C CA 2212405C CA 002212405 A CA002212405 A CA 002212405A CA 2212405 A CA2212405 A CA 2212405A CA 2212405 C CA2212405 C CA 2212405C
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/68—Treatment of water, waste water, or sewage by addition of specified substances, e.g. trace elements, for ameliorating potable water
- C02F1/683—Treatment of water, waste water, or sewage by addition of specified substances, e.g. trace elements, for ameliorating potable water by addition of complex-forming compounds
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/28—Treatment of water, waste water, or sewage by sorption
- C02F1/281—Treatment of water, waste water, or sewage by sorption using inorganic sorbents
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/5236—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
- C02F1/5245—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents using basic salts, e.g. of aluminium and iron
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/58—Treatment of water, waste water, or sewage by removing specified dissolved compounds
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/58—Treatment of water, waste water, or sewage by removing specified dissolved compounds
- C02F1/62—Heavy metal compounds
- C02F1/64—Heavy metal compounds of iron or manganese
- C02F1/645—Devices for iron precipitation and treatment by air
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/5236—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/66—Treatment of water, waste water, or sewage by neutralisation; pH adjustment
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/105—Phosphorus compounds
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/16—Nitrogen compounds, e.g. ammonia
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/34—Nature of the water, waste water, sewage or sludge to be treated from industrial activities not provided for in groups C02F2103/12 - C02F2103/32
- C02F2103/40—Nature of the water, waste water, sewage or sludge to be treated from industrial activities not provided for in groups C02F2103/12 - C02F2103/32 from the manufacture or use of photosensitive materials
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S210/00—Liquid purification or separation
- Y10S210/902—Materials removed
- Y10S210/906—Phosphorus containing
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S210/00—Liquid purification or separation
- Y10S210/902—Materials removed
- Y10S210/906—Phosphorus containing
- Y10S210/907—Phosphate slimes
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S423/00—Chemistry of inorganic compounds
- Y10S423/09—Reaction techniques
- Y10S423/14—Ion exchange; chelation or liquid/liquid ion extraction
Abstract
A method for treating phosphate-containing waste water comprising treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) :
M1-x2+M x3+(OH-)2+x-y(A N-)y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of Al3+ and Fe3+, A n- represents n-valent anion, 0.1<=x<=0.5, 0.1<=y<=0.5 and n is 1 or 2 to adsorb phosphate is provided.
M1-x2+M x3+(OH-)2+x-y(A N-)y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of Al3+ and Fe3+, A n- represents n-valent anion, 0.1<=x<=0.5, 0.1<=y<=0.5 and n is 1 or 2 to adsorb phosphate is provided.
Description
' -1-METHOD FOR TREATING WASTE WATER
Field of the Invention The invention relates to a method for treating -- waste water and an agent for treating waste water.
Background Art In recent years, organic materials and nutrients such as nitrates, nitrites, ammonia and phosphates which are contained in industrial effluent and domestic waste water in large amounts are pointed out as a cause of eutrophication leading to red tide in the nearly seas and a cause of pollution of like stimulating multiplication of algae. It is said that the critical concentration of nitrogen compounds (nitrates and nitrites) and phosphates are 0.15 ppm and 0.02 ppm, respectively. The establishment of technology for removing such organic materials and nutrients from the region of higher concentration to the region of lower concentration are earnestly desired.
Methods for removing phosphates from waste water are divided roughly into biological treatmemt methods and physicochemical treatment methods. A
coagulating sedimentation method using coagulant to remove phosphates as slightly soluble salts is a general method as physicochemical treatment methods from the viewpoint of economy and efficiency. Said methods has subjects to be examined such as effusion of salts from coagulants to waste water, sludge treatment, recovery and recycle of phosphates, and insufficient removal of -- phosphates in the region of lower concentration thereof.
A method for adsorbing phosphates using a phosphate adsorbent to remove phosphates is tried other than the coagulating sedimentation method. In carrying out the adsorption method, aluminium hydroxide gel, magnesium oxide, titanium oxide-active carbon complex, zirconium oxide-active carbon complex, volcanic ash soil and the like are examined as a phosphate adsorbent.
In recent years, one of particularly noted water-related enviromental problems is an issue of eutrophication in the closed water areas such as swamp and lake, river and the nearly seas. Japanese government enacts the law to protect lake and marsh as a measure of said problem. Restriction concerning discharge of phosphate, one of nutrients, becomes strict more and more. The present process for treating waste water without dephosphorization step is not enough to follow the restriction with respect to phosphate so that an appropriate phosphate-treating step is needed to be incorporated therein. Under such background, a phosphate adsorbent capable of efficiently recovering and removing phosphates from waste water and capable of recycling ' -3-phosphates from the viewpoint of effective use of resources and post-treatment of the phosphate adsorbent is needed. In addition, as a major cause of - eutrophication, The inflow of phosphates-containing waste water from areas where a sewerage and equipment for treating waste water are not installed due to limitation of land form and straggling houses is pointed out as a major cause of eutrophication. Since treatment of waste water relies on a septic tanc of each house in the areas, an incorporation of dephosphorization step in the phosphate-treatment procedure at a septic tanc is important. In that case, a high-performance and renewable phosphate adsorbent is needed.
A 1.0 to 1.5 m3 of drain having a phosphate concentration of 5-500 ppm per month per general house is discharged in a farm area. With respect to a large-sized septic tanc applied to a group of 10 people or more, phosphates may be removed by coagulation and sedimentation using coagulant containing iron salt or aluminium salt as a major ingredient. In contrast, with respect to a small-sized septic tanc applied to a group of 5-10 people, a coagulant may not be substantially used to remove phosphates because of low efficiency, a phosphate adsorbent is needed. Conditions needed for the phosphate adsorbent applied to a small-sized septic tanc is basically the same as a phosphate adsorbent applied to an equipment for waste water treatment. Since the septic tanc may not be enlarged due to conditions to be -- installed, and a frequency and cost of maintenance are important, it is needed for the phosphate adsorbent not to demand enlargement of the small-sized septic tanc and not to increase a frequency and cost of maintenance.
Further, removal of phosphates, nitrates and nitrites is preferred, since not only phosphates but also nitrates and nitrites cause eutrophication. As the pressure for lower phosphate concentration is increase in the future, it is predicted that decrease of a phosphate concentration not more than 0.02 ppm, the critical concentration of generation of red tide, will be essential. Therefore, phasphate adsorbents useful for removal of phosphate from not only waste water with a higher phosphate concentration but also rivers with.a lower phosphate concentration are necessary.
It is an object of the invention to provide a reasonable method for treating phosphates-contai.~.ing waste water and recovering phosphates comprising treating waste water by a phosphate adsorbent having a large capacity of phosphates adsorption and recycling the phosphate adsorbent.
It is another object of the invention to provide an agent for treating waste water capable of removing phosphates, nitrates and nitrites.
Brief Description of the Drawings -- Fig. 1 demonstrates results of X-ray diffraction with respect to samples obtained in examples 1-7.
Fig. 2 is a flow chart showing a method for treating phosphates-containing waste water in the order conducted.
Fig. 3 is a chart showing the relationship between a phosphorous concentration and a stirring time:
Disclosure of the Invention The invention provides the following method and agent for treating waste water.
Item 1. A method for treating phosphate-containing waste water comprising treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+~OH )2+x-y~An )y/n ~l) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of ' -6-A13+ and Fe3+, An represents n-valent anion, 0.1<_x<_0.5, O.lsy<_0.5 and n is 1 or 2 to adsorb phosphate.
Item 2. A method for treating phosphate-containing waste water according to item 1 comprising the steps of:
step (I) . treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of A13+ and Fe3+, An represents n-valent anion, 0.1<_x<_0.5, 0.1<_y<_0.5 and n is 1 or 2 to adsorb phosphate; and step (II) . treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with at least one phosphate-desorbing agent selected from the group consisting of alkaline metal salts and alkaline earth metal salts other than alkaline metal carbonates and alkaline earth metal carbonates to regenerate and recycle the phosphate adsorbent.
Item 3. A method for treating phosphate-containing waste water according to item 1 comprising the steps of:
_7_ step (I) . treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein MZ+, M3+~ An-~ x~ y and n are as defined above.
to adsorb phosphate;
step (Ia) . treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with an aqueous solution containing an alkaline metal carbonate or an An ion to desorbing and recovering phosphates;
step (Ib) . calcinating the phosphate adsorbent after dephosphorization of step (Ia) at about 430-600 °C;
step (II) . treating the phosphate adsorbent after calcination with at least one phosphate-desorbing agent selected from the group consisting of alkaline metal salts and alkaline earth metal salts other than alkaline metal carbonates and alkaline earth metal carbonates to regenerate and recycle the phosphate adsorbent.
Item 4. A method for treating phosphate-containing waste water according to item 1 comprising the steps of:
step (I) . treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
_8_ M1_x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+, M3+~ An-~ x~ Y and n are as defined above.
to adsorb phosphate;
step (Ia) . treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with an aqueous solution containing an alkaline metal carbonate or an An ion to desorb and recover phosphates;
step (Ic) . dissolving the phosphate-desorbed phosphate adsorbent in an acidic solution to recycle the solution as raw material for producing a phosphate adsorbent.
Item 5. A method for treating phosphate-containing waste water according to item 1 comprising the steps of:
step (III) . treating the calcinated phosphate adsorbent obtained in step (Ib) of item 3 with phosphate-containing waste water; and step (IV) . repeating the step (II) of item 2 or the steps (Ia), (Ib) and (II) of item 3 using the phosphate-adsorbed phosphate adsorbent obtained in the step (III).
Item 6. A method for treating phosphate-containing waste water according to item 1 comprising dissolving the calcinated phosphate adsorbent obtained in step (Ib) of item 3 in an acidic solution to recycle the solution as raw material for producing a phosphate adsorbent.
Item 7. An agent for removing phosphates, nitrates and _9_ nitrites from waste water comprising a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+, M3+~ An-~ x~~Y and n are as defined above.
Item_8. A granulate of phosphate adsorbent for treating phosphate-containing waste water comprising about 99-60 by weight of a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+, M3+~ An-~ x~ Y and n are as defined above and about 1-40 a by weight of a binder.
Item 9. The granulate according to item 8 wherein said binder comprises an aminated polyacrylamide.
Item 10. The granulate according to. item 8 wherein said binder comprises about 99-6G % by weight of an aminated polyacrylamide and about 1-40 % by weight of at least one selected from the group consisting of polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and stylene/acryl resin.
' -10-The metal hydroxide complex used in the invention is represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+~
Fe2+,.Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of A13+ and Fe3+, An represents n-valent anion, 0.1<_xs0.5, 0.1<_y<_0.5 and n is 1 or 2 to adsorb phosphate Divalent metal ions represented by M2+ include 2+ 2+ 2+ 2+ 2+ 2+ 2+
Mg , Ni , Zn , Fe , Ca and Cu , preferably Mg and Ca2+. Trivalent metal ions represented by M3+
include A13+ and Fe3+, preferably Fe3+.
An represents n-valent anion (n=1 or 2). An may consists of one or more monovalent ion, one or more divalent ion or both of monovalent ions) and divalent ion(s). When An includes a monovalent ion and a divalent ion, a molar ratio of the divalent ion is preferably less than a molar ratio of the monovalent ion.
Monovalent anions include OH , C1 , N02 , N03 , F , Br and HC03 , preferably C1 . Divalent anions include 5042 , C032 and 5032 , preferably S042 .
With respect to x, usually 0.1<-x<_0.5, preferably 0.2<-x<_0.4, more preferably 0.2<_x<-0.35.
With respect to y, usually 0.1<_y<_0.5, preferably 0.2<_y<_0.4, more preferably 0.2<_y<_0.35.
With respect to the compound of formula (1), divalent metal ions M2+, trivalent metal ions M3+ and a carbonate ion are determined by titration. A C1 ion is determined by an ion meter provided with a chlorine ion selective electrode. An ions comprising N02 , N03 , F , Br , HC03 and like monovalent ions and 5042 , 5032 and like divalent ions are determined by ion chromatography.
The "y" value with respect to divalent ions is demonstrated by the measured mole value of A2 . A molar ratio of hydroxide ion OH is calculated by using measured values of M2+, M3+ and An to electrically neutralize the metal hydroxide complex.
When phosphates, nitrates and nitrites should be removed simultaneously, monovalent ions of An may include halogen ions (C1 , F , Br ) and hydroxide ion except for N02 and N03 . C1 ion is most preferable from the viewpoint of enviromental protection.
Said metal hydroxide complex may be used individually or a mixture of two or more. With respect to shape thereof, the metal hydroxide complex may be used in the form of powder. However, the metal hydroxide complex is preferably in the form of granulate and filter medium. Binders for granulation are not specifically limited. The binders include polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin, styrene/acryl resin and aminated polyacrylamides (eg.
polyacrylic hydrazide) and like organic resin compounds;
ethyl cellulose, carboxymethyl cellulose and like celluloses; carrageenan, and like polysaccharides. The organic resin compounds are preferably used. Binders preferably include organic resin compounds such as aminated polyacrylamide, more preferably aminated polyacrylamide.
Aminated polyacrylamide and other binders may be blended. Other binders blended with aminated polyacrylamide include at least one of polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and styrene/acryl resin.
When aminated polyacrylamide is used as a binder, a small amount of aminated polyacrylamide is enough to produce granulates with improved mechanical strength and phosphate adsorption capacity. In order to improve workability during granulation by lowering viscosity of the mixture, other binders such as polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and styrene/acryl resin are preferably combined with aminated polyacrylamide. Using the mixture of aminated polyacrylamide with any of polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and styene/acryl resin as a -- binder makes it possible to produce granulates with improved properties such as mechanical strength, phosphate-adsorption capacity and workability. Binders may be added in an amount of about 1-40 % by weight, preferably about l-20 % by weight, more preferably about 1-10 % by weight based on the total amount of granulates.
As a binder, a mixture of aminated polyacrylamide with at least one of polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and styrene/acryl resin in an amount about 1-40 % by weight, preferably about 1-20 % by weight, more preferably about 1-10 % by weight which is used based on the amount of aminated polyacrylamide may be used. A preferable method for producing granurates comprises adding a necessary amount of water to a mixture of about 99-60 % by weight of a metal hydroxide complex and about 1-40 % by weight of said binder composition, kneading the mixture sufficiently, and forming shaped particles with a granulator. Conventional kneaders and granulators may be used. As a kneader, kneaders provided with binary rotating shafts are preferable. As a granulator, upstroke-type extrusion granulators may be preferably used. The shaped particles are dried and hardened to give granulates of the invention. Drying and hardening are carried out at not less than the lowest -- temperature of membrane-forming of binders or more to dry the granules. Drying below the membrane-forming temperature is possible when drying is conducted for an extended period.
The metal hydroxide complex of the invention used as a phosphate adsorbent may capture a phosphate ion by an anion exchange reaction between an n-valent anion (n=1 or 2) in the composition and a phosphate ion. Tree captured phosphate ion may be desorbed by using solutions of alkaline metal carbonates, alkaline metal salts and alkaline earth metal salts as a desorbing solution.
The phosphate ion desorbing solution is preferably aqueous solution of alkaline metal carbonates or hydrogen carbonates, such as sodium carbonate, potassium carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, ammonium carbonate and lithium carbonate, preferably aqueous solutions of sodium carbonate and sodium i~ydrogen carbonate. Aqueous alkaline metal solutions preferably include aqueous solutions of ammonium hydroxide, sodium hydroxide, potassium hydroxide, sodium chloride, potassium chloride, sodium fluoride, potassium fluoride, sodium bromide, ' -15-potassium bromide, sodium sulfate, potassium sulfate, sodium sulfite and potassium sulfite, more preferably aqueous solutions of sodium hydroxide and sodium -- chloride. Aqueous alkaline earth metal solutions preferably include aqueous solutions of magnesium chloride, calcium chloride, magnesium sulfate, magnesium bromide and calcium bromide, more preferably aqueous solutions of magnesium chloride. and magnesium sulfate.
Treatment of a phosphate adsorbent with such a desorbing solution makes it possible to recover and recycle w phosphates from a phosphate-adsorbed phosphate adsorbent.
When waste water contains phosphates and nitrogen components (nitrate and nitrite), phosphates and nitrogen components may be recovered by treatment with the desorbing solution.
Because the metal hydroxide complex shows endothermic peaks at about 380 °C and about 430 °C based on an endothermic reaction accompanied by decomposition thereof when heat-treatment of the complex at about 250-550 °C, the metal hydroxide complex after phosphate desorption may be calcinatea at a temperature of decomposition or more, i.e., about 430-600 °C, preferably about 550 °C to generate a metal hydroxide complex without an anionic residue acting as an ion-exchange group.
By utilyzing the property that a metal oxide complex is converted to a metal hydroxide complex when bringing the complex into contact with an anion-containing electrolyte solution, a metal hydroxide complex having n-valent anion as an ion-exchane group may be regenerated by stirring a metal oxide complex in an electrolyte solution containing n-valent anion. Such electrolyte solutions include sodium chloride, potassium chloride, ammonium chloride and lithium chloride, preferably sodium chloride because of low cost. A
concentration of the electrolyte solution ranges from about 0.5 M to about 5 M, and regeneration time ranges from about 2 to about 4 hours. Regeneration of a phosphate-adsorbed phosphate adsorbent may be carried out after treatment of waste water with a metal oxide complex.
Since a metal hydroxide complex and metal oxide complex may be dissolved in an acidic solution with a pH
of 5 or less, recycling of an acidic solution in which a metal hydroxide complex and a metal oxide complex are dissolved as a raw material to prepare metal hydroxide complex. The acidic solutions include hydrochloric acid, aluminium chloride, ferric chloride, preferably hydrochloric acid.
Regeneration of the metal hydroxide complex after acid treatment may be easily carried out according to a document (Langmuir, 9, 1418-1422 (1993)).
Dephosphorization capacity of phosphate - adsorbent is efficiently regenerated by using a phosphate ion desorbing solution. The phosphate adsorbent after phosphate adsorption may be regenerated in a phosphate ion desorbing solution containing one or more alkaline metal_salts and alkaline earth metal salts except for alkaline metal carbonates. Preferable alkaline metal salts used in the regeneration process include sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium chloride, potassium chloride and lithium chloride, preferably sodium hydroxide and sodium chloride.
Preferable alkaline earth metal salts used in the regeneration process include magnesium chloride, magnesium sulfate, magnesium nitrate, calcium chloride and calcium nitrate, preferably magnesium chloride and magnesium sulfate. The regeneration process may comprise a treatment with an aqueous solution of alkaline metal salts and a treatment with aqueous solution of alkaline earth metal salts in combination for several times.
According to the invention, phosphates in waste water may be adsorbed efficiently by using a phosphate adsorbent containing metal hydroxide complex with large phosphate adsorption capacity, phosphates may be recovered and recycled efficiently with low cost, and the phosphate adsorbent may be regenerated. The process and agent of the invention may be applied to a variety of equipments for waste water treatment and purification of river, and also may miniaturize the equipment to lower maintenance frequency and cost when applied to a family-type waste water treatment such as septic tank. In particular, the phosphate adsorbent may be regenerated so that a secondary enviromental pollution will not be caused by disposal of the phosphate adsorbent.
Phosphates adsorbed may be recovered and~recycled as resources, which is very effective from the viewpoint of prevention of eutrophication and water-related enviromental protection.
In addition, the agent for waste water treatment of the invention is very preferable, because the agent may remove both phosphates and nitrogen components such as nitrates and nitrites.
Examples The invention will be described below in detail using examples, but the invention is in.no way limited to the examples.
Example 1 A 20 g of phosphate adsorbent (Mg2+0-665Fe3+0.335(OH ~2.099C1 0.124(C032 X0.056' ' -19-hereinafter referred to as "C1/HT-Fe") was added to an aqueous solution of Na2HP04 (1600cm3) having a phosphate concentration of 26.7 mM-P, and the mixture was stirred -- at 25 °C for 4 hours. After stirring, the phosphate adsorbent was filtered off. A phosphate ion concentration in the filtrate was determined by molybdenum blue method.
The amount of adsorbed phosphate ion was calculated as adsorption per 1 g of the phosphate adsorbent by subtracting remaining phosphate ion concentration after adsorption equilibrium from initial phosphate ion concentration. A pH of the aqueous solution during phosphate ion adsorption was adjusted to pH 6.93.
The adsorbed amount of phosphorus is 1.17 mmolP/g.
When another phosphate adsorbent (Mg2+0.683A13+0.317(OH )2.03301 0.238(0032 )0.023' hereinafter referred to as "C1/HT-A1") was evaluated in place of C1/HT-Fe in the same manner as above, the adsorbed amount of phosphorus is 2.13 mmolP/g.
Example 2 In order to desorb phosphate, 16 g of the phosphate-containing phosphate adsorbent obtained in example 1 (hereinafter referred to as "P/HT-Fe" and "P/HT-A1") was added to 2M-Na2C03 aqueous solution (1280cm3), respectively, to exchange phosphate ion for carbonate ion. After stirring at 90 °C for 4 hours, each phosphate adsorbent was filtered off. After washing with water, drying and dissolving in hydrochloric acid solution, a phosphate ion concentration of the filtrate was determined in the same manner as example 1 to calculate the remaining phosphorus in the phosphate adsorbents. With respect to P/HT-Fe and P/HT-A1, the remaining phosphorus concentrations are determined 0.09mmo1P/g and 0.29 mmolP/g, respectively, indicating that about 90 0 of phosphorus are desorbed in each sample.
Example 3 The phosphate adsorbents obtained in example 2 after phosphate desorption (hereinafter referred to as "C03/HT-Fe" and "C03/HT-A1") was calcinated at 550 °C for 3 hours to prepare metal oxide complex. The metal oxide complex powders were subjected to X-ray diffraction analysis. The results of the analysis demonstrate that the metal oxide complexes have X-ray patterns caused by magnesium oxide structure.
Example 4 A 5 g of each metal oxide complex (hereinafter referred to as "MgFeO" and "MgAlO", respectively) was added to 5M-NaCl aqueous solution (400cm3), respectively.
The resulting mixtures were stirred at 90 °C for 4 hours.
After filtration, washing with water and drying, the resulting powders were subjected to X-ray diffraction analysis. The results of the analysis demonstrate regeneration of metal hydroxide complexes (Cl/HT-Fe and C1/HT-A1), respectively.
Example 5 The regenerated phosphate adsorbent (C1/HT-Fe) obtained in example 4 (1 g) was added to an aqueous solution of Na2HP04 (80cm3) having a phosphate concentration of 26.7 mM-P, and the mixture was stirred at 25 °C for 4 hours. After stirring, the phosphate adsorbent was filtered off. A phosphate ion concentration of the filtrate was determined in the same manner as example 1 to determine adsorption of phosphate ion: The adsorbed amount of phosphorus is 1.00 mmolP per 1 g of the regenerated phosphate adsorbent (C1/HT-Fe).
The adsorbed amount (1.00 mmolP/g) corresponds t~ about 85 % of the initial phosphate adsorbent (1.17 mmolP/g).
Example 6 A 3 g of the metal hydroxide complex and 3 g of the metal oxide complex obtained in examples 2 and 3 were dissolved in a 6N-hydrochloric acid solution, respectively, to prepare a mixed solution (100 ml) of MgCl2 + FeCl3 (Mg/Fe molar ratio = 1.99) and a mixed solution (100m1) of MgCl2 + A1C13 (Mg/A1 molar ratio =
2.15). The mixed solutions were boiled to remove carbon dioxide. Metal hydroxide complexes C1/HT-Fe (Mg2+0.651Fe3+0.349(OH )2.18301 0.090(0032 )0.038 and C1/HT-A1 (Mg2~0.676A13+0.324(OH )2.08201 0.214(0032 )0.014) were then prepared according to a method described by Langmuir, 9, 1418-1422 (1993). The adsorbed amounts of phosphorus determined in the same manner as example 1 are 0.97 mmolP/g with respect to Cl/HT-Fe and 2.13 mmolP/g with respect to C1/HT-A1, respectively.
Example 7 The metal oxide complexes (1 g) obtained in example 3 were added to a Na2HP04 aqueous solution (80cm3) having a phosphate concentration of 26.7 mM-P, and the mixtures was stirred at 25 °C for 4 hours, respectively. After stirring, each phosphate adsorbent was filtered off. Phosphate ion concentrations of filtrates determined in the same manner as example 1 are 1.00 mmolP/g with respect to MgFeO and 0.87 mmolP/g with respect to MgAlO.
For the purpose of desorption of phosphate, 0.3 g of phosphate-containing phosphate adsorbents thus ' -23-obtained (hereinafter referred to as "P/MgFeO" and "P/MgAlO") were added to 2M-Na2C03 aqueous solution (24cm3), respectively, to exchange phosphate ion for carbonate ion. After stirring at 90 °C for 2 hours, each phosphate adsorbent was filtered off. After washing with water, drying and dissolving in hydrochloric acid solution, phosphate ion concentrations of the filtrates were determined in the same manner as example 1 to calculate the remaining phosphorus in the phosphate adsorbents. With respect to P/MgFeO and P/MgAlO, the remaining phosphorus are determined as O.lOmmolP/g and 0.47 mmolP/g, respectively, indicating that phosphorus of P/MgFeO was desorbed about 90 %, and that phosphorus of P/MgAlO was desorbed about 46 %. The phosphate adsorbent powders after phosphate desorption treatment were subjected to X-ray diffraction analysis. The results of the analysis demonstrate that C03/HT-Fe and C03/HT-A1 structures are regenerated. The regenerated phosphate adsorbents may be used according to the methods of examples 3, 4 or 6.
Example 8 A 0.01 g of phosphate adsorbent, C1/HT-Fe or C1/HT-A1 was added to model waste water (40 ml) containing a variety of ions (2.0 ppm-P; 10.4 ppm-N02 ;
7.0 ppm-N03 ; and 16.5 ppm-S042 ). The mixture was stirred at room temperature for 4 hours. After stirring, the phosphate adsorbent was filtered off. A phosphate ion concentration in the filtrate was determined in the same manner as example 1, and other ions in the filtrate were determined by ion chromatography. The results are shown in table 1. Table 1 demonstrates that not only phosphate but also other ions are significantly reduced by treating the model waste water with the phosphate adsorbents.
Table 1 Agent for treating Ion concentration (ppm).
waste water P N02- N03- S04-_ C1/HT-Fe 0.7 2.9 1.5 12.1 C1/HT-A1 0.2 2.4 1.1 8.0 Example 9 A 0.5 g of the phosphate-containing phosphate adsorbent (P/HT-A1) was added to an Erlenmeyer flask with ground stopper to which a 6 % NaOH + 30% NaCl mixed solution (20 ml) was added. The mixture was shaked laterally (170 shake/min) for 4 hours. The phosphate adsorbent was filtered~off and the agent was washed with water. The phosphate adsorbent was subjected to the shaking treatment as above using 79.3 % MgCl2 aqueous solution. The amount of desorbed phosphate ion was calculated as adsorption per 1 g of the phosphate adsorbent by determining a phosphate concentration of the filtrate according to the method of example 1. The desorbed amount of phosphorus is 1.73 mmolP/g.
Example 10 -- The desorbed amount of phosphorus is determined in the same manner as example 9 except that the phosphate adsorbent was treated with 3% NaOH aqueous solution and 79.3 % MgCl2 aqueous solution in this sequence as solution for desorption.
The desorbed amount of phosphorus is 1.50 mmolP/g.
Example 11 The regenerated phosphate adsorbents obtained in examples 9 and 10 were treated in the same manner as example 1 to determine the adsorbed amount of phosphorus.
The adsorbed amounts of phosphorus are 1.79 mmolP/g (example 9) and 1.65 mmolP/g (example 10). The regeneration percents of phosphate adsorbents are as high as 84% and 77% based on the saturated phosphorus adsorption of the phosphate adsorbent C1/HT-A1, 2.13 mmolP/g.
Example 12 A suitable amount of polyacrylic hydrazide and polyamide/epichlorohydrin resin as a binder were added to 4 kg of phosphate adsorbent (Cl/HT-A1). The resulting mixture was kneaded with a kneader (output = 1.5 kw;
total volume = 20 liter; binary shaft number of revolution = 29.20 rpm) under conditions of mixing time between phosphate adsorbent and binder (= 1 minute) and kneading time after adding a required amount of water (_ 5 minutes). Granulates (diameter = 3 mm; length = 5-10 mm) were prepared with upstroke-type extrusion granulators (output = 3.7 kw; screen = 3 mm ; number of revolution = 135 rpm), and the granulates were dried at 80 °C for 15 hours.
Example 13 The granulates obtained in example 12 were subjected to a strength test and a phosphate-adsorption test. The strength test was carried out according to the following procedure. A 1.0 g of accurately weighed granulates and 20 ml of water were added to an Erlenmeyer flask with ground stopper. The flask was shaked with lateral-shake thermostat at 30°C, 170 shake/min for 3 hours. After filtration and drying, a total weight of the granulates were determined. The resulting granulates were sieved with 10-mesh sieve to weigh residue on sieve and sieve-passed fraction. Lrushing resistance strength (L) is calculated by the following equation.
Crushing resistance strength = 100 - {P/(S + P)~ x 100 wherein P = weight of 10-mesh sieve-passed fraction; and S = weight of residue on 10-mesh sieve. Crushing resistance strength is practically needed 85 or more.
The phosphate adsorption test was conducted according to the following procedure.
A 1.0 g of granulates was accurately weighed and added to an Erlenmeyer flask with ground stopper. A
20 ml of the aqueous solution of Na2HP04 used in example 1 was added thereto. The flask was laterally shaked at 30°C,_170 shake/min for 3 hours. After filtration, a phosphate concentration of the filtrate was determined in the same manner as example 1 to calculate the amount of phosphate adsorbed. The results were shown in table 2.
Table 2 Binder Loading Capacity Adsorbed Crushing of of binder granulator phosphate resistance (wt.%) (kq/hr) (mmolP/q) stren t~ h Poly-acrylic 1.0 70 0.69 86.4 h~drazide Poly-acrylic 3.0 60 0.60 99.5 hydrazide Polyamide epichloro- 5.0 150 1.28 33.5 hydrine resin Poly-acrylic 1.0 hydrazide Polyamide 110 0.67 97.3 epichloro-hydrine 4.0 resin The results of table 2 show that the phosphate adsorbent of the invention meets the waste water quality standard with respect to a septic tank, sewerage, waste water from village. The phosphate adsorbent of the invention will be applicable to the more strict standard.
Example 14 The granulates obtained in example 12 were ground. A predetermined amount of the ground product (particle size : 200-280 mesh) was added to an aqueous NaH2P04 solution (2,000 ml, pH=6.8) adjusted to a phosphorous concentration of lppm-P, and the resulting mixture was stirred at 25 °C so as to determine the change of a phosphorous concentration relative to a stirring time. Determmination of the phosphorous concentration were carried out in the same manner as example 1. The results are shown in fig.3. Fig.3 shows that a rate of phosphate adsorption increases with the increase of the added amount of the ground product and that phosphate was removed and adsorbed withis 10 minutes from the addition of the phosphate adsorbent (0.025 %) thereto.
Example 15 Phosphate adsorption capacity of a phosphate adsorbent was evaluated using waste water with a low phosphate concentration. The waste water was collected from an equipment for waste water treatment located in a farm area in KASHIMA-cho, SHIMANE-ken JAPAN. The phasphate adsorbent (C1/HT-Al, O.lg) was added to the waste water (400 ml). The resulting mixture was strred with a magnetic stirrer for 4 hours. After stirring, the treated water was filtered with a 0.45um-membrane filter to analyze the phosphate concentration of the filtrate according to the assay method defined by Japanese ,Industrial Standard (JIS). The phosphate concentration of the waste water (0.18 ppm-P) was decreased by the treatment below detection limit of phosphate showing usefulness of the phosphate adsobent of the invention when applied to waste water with low phosphate concentration.
Field of the Invention The invention relates to a method for treating -- waste water and an agent for treating waste water.
Background Art In recent years, organic materials and nutrients such as nitrates, nitrites, ammonia and phosphates which are contained in industrial effluent and domestic waste water in large amounts are pointed out as a cause of eutrophication leading to red tide in the nearly seas and a cause of pollution of like stimulating multiplication of algae. It is said that the critical concentration of nitrogen compounds (nitrates and nitrites) and phosphates are 0.15 ppm and 0.02 ppm, respectively. The establishment of technology for removing such organic materials and nutrients from the region of higher concentration to the region of lower concentration are earnestly desired.
Methods for removing phosphates from waste water are divided roughly into biological treatmemt methods and physicochemical treatment methods. A
coagulating sedimentation method using coagulant to remove phosphates as slightly soluble salts is a general method as physicochemical treatment methods from the viewpoint of economy and efficiency. Said methods has subjects to be examined such as effusion of salts from coagulants to waste water, sludge treatment, recovery and recycle of phosphates, and insufficient removal of -- phosphates in the region of lower concentration thereof.
A method for adsorbing phosphates using a phosphate adsorbent to remove phosphates is tried other than the coagulating sedimentation method. In carrying out the adsorption method, aluminium hydroxide gel, magnesium oxide, titanium oxide-active carbon complex, zirconium oxide-active carbon complex, volcanic ash soil and the like are examined as a phosphate adsorbent.
In recent years, one of particularly noted water-related enviromental problems is an issue of eutrophication in the closed water areas such as swamp and lake, river and the nearly seas. Japanese government enacts the law to protect lake and marsh as a measure of said problem. Restriction concerning discharge of phosphate, one of nutrients, becomes strict more and more. The present process for treating waste water without dephosphorization step is not enough to follow the restriction with respect to phosphate so that an appropriate phosphate-treating step is needed to be incorporated therein. Under such background, a phosphate adsorbent capable of efficiently recovering and removing phosphates from waste water and capable of recycling ' -3-phosphates from the viewpoint of effective use of resources and post-treatment of the phosphate adsorbent is needed. In addition, as a major cause of - eutrophication, The inflow of phosphates-containing waste water from areas where a sewerage and equipment for treating waste water are not installed due to limitation of land form and straggling houses is pointed out as a major cause of eutrophication. Since treatment of waste water relies on a septic tanc of each house in the areas, an incorporation of dephosphorization step in the phosphate-treatment procedure at a septic tanc is important. In that case, a high-performance and renewable phosphate adsorbent is needed.
A 1.0 to 1.5 m3 of drain having a phosphate concentration of 5-500 ppm per month per general house is discharged in a farm area. With respect to a large-sized septic tanc applied to a group of 10 people or more, phosphates may be removed by coagulation and sedimentation using coagulant containing iron salt or aluminium salt as a major ingredient. In contrast, with respect to a small-sized septic tanc applied to a group of 5-10 people, a coagulant may not be substantially used to remove phosphates because of low efficiency, a phosphate adsorbent is needed. Conditions needed for the phosphate adsorbent applied to a small-sized septic tanc is basically the same as a phosphate adsorbent applied to an equipment for waste water treatment. Since the septic tanc may not be enlarged due to conditions to be -- installed, and a frequency and cost of maintenance are important, it is needed for the phosphate adsorbent not to demand enlargement of the small-sized septic tanc and not to increase a frequency and cost of maintenance.
Further, removal of phosphates, nitrates and nitrites is preferred, since not only phosphates but also nitrates and nitrites cause eutrophication. As the pressure for lower phosphate concentration is increase in the future, it is predicted that decrease of a phosphate concentration not more than 0.02 ppm, the critical concentration of generation of red tide, will be essential. Therefore, phasphate adsorbents useful for removal of phosphate from not only waste water with a higher phosphate concentration but also rivers with.a lower phosphate concentration are necessary.
It is an object of the invention to provide a reasonable method for treating phosphates-contai.~.ing waste water and recovering phosphates comprising treating waste water by a phosphate adsorbent having a large capacity of phosphates adsorption and recycling the phosphate adsorbent.
It is another object of the invention to provide an agent for treating waste water capable of removing phosphates, nitrates and nitrites.
Brief Description of the Drawings -- Fig. 1 demonstrates results of X-ray diffraction with respect to samples obtained in examples 1-7.
Fig. 2 is a flow chart showing a method for treating phosphates-containing waste water in the order conducted.
Fig. 3 is a chart showing the relationship between a phosphorous concentration and a stirring time:
Disclosure of the Invention The invention provides the following method and agent for treating waste water.
Item 1. A method for treating phosphate-containing waste water comprising treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+~OH )2+x-y~An )y/n ~l) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of ' -6-A13+ and Fe3+, An represents n-valent anion, 0.1<_x<_0.5, O.lsy<_0.5 and n is 1 or 2 to adsorb phosphate.
Item 2. A method for treating phosphate-containing waste water according to item 1 comprising the steps of:
step (I) . treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of A13+ and Fe3+, An represents n-valent anion, 0.1<_x<_0.5, 0.1<_y<_0.5 and n is 1 or 2 to adsorb phosphate; and step (II) . treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with at least one phosphate-desorbing agent selected from the group consisting of alkaline metal salts and alkaline earth metal salts other than alkaline metal carbonates and alkaline earth metal carbonates to regenerate and recycle the phosphate adsorbent.
Item 3. A method for treating phosphate-containing waste water according to item 1 comprising the steps of:
_7_ step (I) . treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein MZ+, M3+~ An-~ x~ y and n are as defined above.
to adsorb phosphate;
step (Ia) . treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with an aqueous solution containing an alkaline metal carbonate or an An ion to desorbing and recovering phosphates;
step (Ib) . calcinating the phosphate adsorbent after dephosphorization of step (Ia) at about 430-600 °C;
step (II) . treating the phosphate adsorbent after calcination with at least one phosphate-desorbing agent selected from the group consisting of alkaline metal salts and alkaline earth metal salts other than alkaline metal carbonates and alkaline earth metal carbonates to regenerate and recycle the phosphate adsorbent.
Item 4. A method for treating phosphate-containing waste water according to item 1 comprising the steps of:
step (I) . treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
_8_ M1_x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+, M3+~ An-~ x~ Y and n are as defined above.
to adsorb phosphate;
step (Ia) . treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with an aqueous solution containing an alkaline metal carbonate or an An ion to desorb and recover phosphates;
step (Ic) . dissolving the phosphate-desorbed phosphate adsorbent in an acidic solution to recycle the solution as raw material for producing a phosphate adsorbent.
Item 5. A method for treating phosphate-containing waste water according to item 1 comprising the steps of:
step (III) . treating the calcinated phosphate adsorbent obtained in step (Ib) of item 3 with phosphate-containing waste water; and step (IV) . repeating the step (II) of item 2 or the steps (Ia), (Ib) and (II) of item 3 using the phosphate-adsorbed phosphate adsorbent obtained in the step (III).
Item 6. A method for treating phosphate-containing waste water according to item 1 comprising dissolving the calcinated phosphate adsorbent obtained in step (Ib) of item 3 in an acidic solution to recycle the solution as raw material for producing a phosphate adsorbent.
Item 7. An agent for removing phosphates, nitrates and _9_ nitrites from waste water comprising a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+, M3+~ An-~ x~~Y and n are as defined above.
Item_8. A granulate of phosphate adsorbent for treating phosphate-containing waste water comprising about 99-60 by weight of a metal hydroxide complex as a phosphate adsorbent represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+, M3+~ An-~ x~ Y and n are as defined above and about 1-40 a by weight of a binder.
Item 9. The granulate according to item 8 wherein said binder comprises an aminated polyacrylamide.
Item 10. The granulate according to. item 8 wherein said binder comprises about 99-6G % by weight of an aminated polyacrylamide and about 1-40 % by weight of at least one selected from the group consisting of polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and stylene/acryl resin.
' -10-The metal hydroxide complex used in the invention is represented by formula (1) .
M1-x2+Mx3+(OH )2+x-y(An )y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+~
Fe2+,.Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of A13+ and Fe3+, An represents n-valent anion, 0.1<_xs0.5, 0.1<_y<_0.5 and n is 1 or 2 to adsorb phosphate Divalent metal ions represented by M2+ include 2+ 2+ 2+ 2+ 2+ 2+ 2+
Mg , Ni , Zn , Fe , Ca and Cu , preferably Mg and Ca2+. Trivalent metal ions represented by M3+
include A13+ and Fe3+, preferably Fe3+.
An represents n-valent anion (n=1 or 2). An may consists of one or more monovalent ion, one or more divalent ion or both of monovalent ions) and divalent ion(s). When An includes a monovalent ion and a divalent ion, a molar ratio of the divalent ion is preferably less than a molar ratio of the monovalent ion.
Monovalent anions include OH , C1 , N02 , N03 , F , Br and HC03 , preferably C1 . Divalent anions include 5042 , C032 and 5032 , preferably S042 .
With respect to x, usually 0.1<-x<_0.5, preferably 0.2<-x<_0.4, more preferably 0.2<_x<-0.35.
With respect to y, usually 0.1<_y<_0.5, preferably 0.2<_y<_0.4, more preferably 0.2<_y<_0.35.
With respect to the compound of formula (1), divalent metal ions M2+, trivalent metal ions M3+ and a carbonate ion are determined by titration. A C1 ion is determined by an ion meter provided with a chlorine ion selective electrode. An ions comprising N02 , N03 , F , Br , HC03 and like monovalent ions and 5042 , 5032 and like divalent ions are determined by ion chromatography.
The "y" value with respect to divalent ions is demonstrated by the measured mole value of A2 . A molar ratio of hydroxide ion OH is calculated by using measured values of M2+, M3+ and An to electrically neutralize the metal hydroxide complex.
When phosphates, nitrates and nitrites should be removed simultaneously, monovalent ions of An may include halogen ions (C1 , F , Br ) and hydroxide ion except for N02 and N03 . C1 ion is most preferable from the viewpoint of enviromental protection.
Said metal hydroxide complex may be used individually or a mixture of two or more. With respect to shape thereof, the metal hydroxide complex may be used in the form of powder. However, the metal hydroxide complex is preferably in the form of granulate and filter medium. Binders for granulation are not specifically limited. The binders include polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin, styrene/acryl resin and aminated polyacrylamides (eg.
polyacrylic hydrazide) and like organic resin compounds;
ethyl cellulose, carboxymethyl cellulose and like celluloses; carrageenan, and like polysaccharides. The organic resin compounds are preferably used. Binders preferably include organic resin compounds such as aminated polyacrylamide, more preferably aminated polyacrylamide.
Aminated polyacrylamide and other binders may be blended. Other binders blended with aminated polyacrylamide include at least one of polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and styrene/acryl resin.
When aminated polyacrylamide is used as a binder, a small amount of aminated polyacrylamide is enough to produce granulates with improved mechanical strength and phosphate adsorption capacity. In order to improve workability during granulation by lowering viscosity of the mixture, other binders such as polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and styrene/acryl resin are preferably combined with aminated polyacrylamide. Using the mixture of aminated polyacrylamide with any of polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and styene/acryl resin as a -- binder makes it possible to produce granulates with improved properties such as mechanical strength, phosphate-adsorption capacity and workability. Binders may be added in an amount of about 1-40 % by weight, preferably about l-20 % by weight, more preferably about 1-10 % by weight based on the total amount of granulates.
As a binder, a mixture of aminated polyacrylamide with at least one of polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and styrene/acryl resin in an amount about 1-40 % by weight, preferably about 1-20 % by weight, more preferably about 1-10 % by weight which is used based on the amount of aminated polyacrylamide may be used. A preferable method for producing granurates comprises adding a necessary amount of water to a mixture of about 99-60 % by weight of a metal hydroxide complex and about 1-40 % by weight of said binder composition, kneading the mixture sufficiently, and forming shaped particles with a granulator. Conventional kneaders and granulators may be used. As a kneader, kneaders provided with binary rotating shafts are preferable. As a granulator, upstroke-type extrusion granulators may be preferably used. The shaped particles are dried and hardened to give granulates of the invention. Drying and hardening are carried out at not less than the lowest -- temperature of membrane-forming of binders or more to dry the granules. Drying below the membrane-forming temperature is possible when drying is conducted for an extended period.
The metal hydroxide complex of the invention used as a phosphate adsorbent may capture a phosphate ion by an anion exchange reaction between an n-valent anion (n=1 or 2) in the composition and a phosphate ion. Tree captured phosphate ion may be desorbed by using solutions of alkaline metal carbonates, alkaline metal salts and alkaline earth metal salts as a desorbing solution.
The phosphate ion desorbing solution is preferably aqueous solution of alkaline metal carbonates or hydrogen carbonates, such as sodium carbonate, potassium carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, ammonium carbonate and lithium carbonate, preferably aqueous solutions of sodium carbonate and sodium i~ydrogen carbonate. Aqueous alkaline metal solutions preferably include aqueous solutions of ammonium hydroxide, sodium hydroxide, potassium hydroxide, sodium chloride, potassium chloride, sodium fluoride, potassium fluoride, sodium bromide, ' -15-potassium bromide, sodium sulfate, potassium sulfate, sodium sulfite and potassium sulfite, more preferably aqueous solutions of sodium hydroxide and sodium -- chloride. Aqueous alkaline earth metal solutions preferably include aqueous solutions of magnesium chloride, calcium chloride, magnesium sulfate, magnesium bromide and calcium bromide, more preferably aqueous solutions of magnesium chloride. and magnesium sulfate.
Treatment of a phosphate adsorbent with such a desorbing solution makes it possible to recover and recycle w phosphates from a phosphate-adsorbed phosphate adsorbent.
When waste water contains phosphates and nitrogen components (nitrate and nitrite), phosphates and nitrogen components may be recovered by treatment with the desorbing solution.
Because the metal hydroxide complex shows endothermic peaks at about 380 °C and about 430 °C based on an endothermic reaction accompanied by decomposition thereof when heat-treatment of the complex at about 250-550 °C, the metal hydroxide complex after phosphate desorption may be calcinatea at a temperature of decomposition or more, i.e., about 430-600 °C, preferably about 550 °C to generate a metal hydroxide complex without an anionic residue acting as an ion-exchange group.
By utilyzing the property that a metal oxide complex is converted to a metal hydroxide complex when bringing the complex into contact with an anion-containing electrolyte solution, a metal hydroxide complex having n-valent anion as an ion-exchane group may be regenerated by stirring a metal oxide complex in an electrolyte solution containing n-valent anion. Such electrolyte solutions include sodium chloride, potassium chloride, ammonium chloride and lithium chloride, preferably sodium chloride because of low cost. A
concentration of the electrolyte solution ranges from about 0.5 M to about 5 M, and regeneration time ranges from about 2 to about 4 hours. Regeneration of a phosphate-adsorbed phosphate adsorbent may be carried out after treatment of waste water with a metal oxide complex.
Since a metal hydroxide complex and metal oxide complex may be dissolved in an acidic solution with a pH
of 5 or less, recycling of an acidic solution in which a metal hydroxide complex and a metal oxide complex are dissolved as a raw material to prepare metal hydroxide complex. The acidic solutions include hydrochloric acid, aluminium chloride, ferric chloride, preferably hydrochloric acid.
Regeneration of the metal hydroxide complex after acid treatment may be easily carried out according to a document (Langmuir, 9, 1418-1422 (1993)).
Dephosphorization capacity of phosphate - adsorbent is efficiently regenerated by using a phosphate ion desorbing solution. The phosphate adsorbent after phosphate adsorption may be regenerated in a phosphate ion desorbing solution containing one or more alkaline metal_salts and alkaline earth metal salts except for alkaline metal carbonates. Preferable alkaline metal salts used in the regeneration process include sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium chloride, potassium chloride and lithium chloride, preferably sodium hydroxide and sodium chloride.
Preferable alkaline earth metal salts used in the regeneration process include magnesium chloride, magnesium sulfate, magnesium nitrate, calcium chloride and calcium nitrate, preferably magnesium chloride and magnesium sulfate. The regeneration process may comprise a treatment with an aqueous solution of alkaline metal salts and a treatment with aqueous solution of alkaline earth metal salts in combination for several times.
According to the invention, phosphates in waste water may be adsorbed efficiently by using a phosphate adsorbent containing metal hydroxide complex with large phosphate adsorption capacity, phosphates may be recovered and recycled efficiently with low cost, and the phosphate adsorbent may be regenerated. The process and agent of the invention may be applied to a variety of equipments for waste water treatment and purification of river, and also may miniaturize the equipment to lower maintenance frequency and cost when applied to a family-type waste water treatment such as septic tank. In particular, the phosphate adsorbent may be regenerated so that a secondary enviromental pollution will not be caused by disposal of the phosphate adsorbent.
Phosphates adsorbed may be recovered and~recycled as resources, which is very effective from the viewpoint of prevention of eutrophication and water-related enviromental protection.
In addition, the agent for waste water treatment of the invention is very preferable, because the agent may remove both phosphates and nitrogen components such as nitrates and nitrites.
Examples The invention will be described below in detail using examples, but the invention is in.no way limited to the examples.
Example 1 A 20 g of phosphate adsorbent (Mg2+0-665Fe3+0.335(OH ~2.099C1 0.124(C032 X0.056' ' -19-hereinafter referred to as "C1/HT-Fe") was added to an aqueous solution of Na2HP04 (1600cm3) having a phosphate concentration of 26.7 mM-P, and the mixture was stirred -- at 25 °C for 4 hours. After stirring, the phosphate adsorbent was filtered off. A phosphate ion concentration in the filtrate was determined by molybdenum blue method.
The amount of adsorbed phosphate ion was calculated as adsorption per 1 g of the phosphate adsorbent by subtracting remaining phosphate ion concentration after adsorption equilibrium from initial phosphate ion concentration. A pH of the aqueous solution during phosphate ion adsorption was adjusted to pH 6.93.
The adsorbed amount of phosphorus is 1.17 mmolP/g.
When another phosphate adsorbent (Mg2+0.683A13+0.317(OH )2.03301 0.238(0032 )0.023' hereinafter referred to as "C1/HT-A1") was evaluated in place of C1/HT-Fe in the same manner as above, the adsorbed amount of phosphorus is 2.13 mmolP/g.
Example 2 In order to desorb phosphate, 16 g of the phosphate-containing phosphate adsorbent obtained in example 1 (hereinafter referred to as "P/HT-Fe" and "P/HT-A1") was added to 2M-Na2C03 aqueous solution (1280cm3), respectively, to exchange phosphate ion for carbonate ion. After stirring at 90 °C for 4 hours, each phosphate adsorbent was filtered off. After washing with water, drying and dissolving in hydrochloric acid solution, a phosphate ion concentration of the filtrate was determined in the same manner as example 1 to calculate the remaining phosphorus in the phosphate adsorbents. With respect to P/HT-Fe and P/HT-A1, the remaining phosphorus concentrations are determined 0.09mmo1P/g and 0.29 mmolP/g, respectively, indicating that about 90 0 of phosphorus are desorbed in each sample.
Example 3 The phosphate adsorbents obtained in example 2 after phosphate desorption (hereinafter referred to as "C03/HT-Fe" and "C03/HT-A1") was calcinated at 550 °C for 3 hours to prepare metal oxide complex. The metal oxide complex powders were subjected to X-ray diffraction analysis. The results of the analysis demonstrate that the metal oxide complexes have X-ray patterns caused by magnesium oxide structure.
Example 4 A 5 g of each metal oxide complex (hereinafter referred to as "MgFeO" and "MgAlO", respectively) was added to 5M-NaCl aqueous solution (400cm3), respectively.
The resulting mixtures were stirred at 90 °C for 4 hours.
After filtration, washing with water and drying, the resulting powders were subjected to X-ray diffraction analysis. The results of the analysis demonstrate regeneration of metal hydroxide complexes (Cl/HT-Fe and C1/HT-A1), respectively.
Example 5 The regenerated phosphate adsorbent (C1/HT-Fe) obtained in example 4 (1 g) was added to an aqueous solution of Na2HP04 (80cm3) having a phosphate concentration of 26.7 mM-P, and the mixture was stirred at 25 °C for 4 hours. After stirring, the phosphate adsorbent was filtered off. A phosphate ion concentration of the filtrate was determined in the same manner as example 1 to determine adsorption of phosphate ion: The adsorbed amount of phosphorus is 1.00 mmolP per 1 g of the regenerated phosphate adsorbent (C1/HT-Fe).
The adsorbed amount (1.00 mmolP/g) corresponds t~ about 85 % of the initial phosphate adsorbent (1.17 mmolP/g).
Example 6 A 3 g of the metal hydroxide complex and 3 g of the metal oxide complex obtained in examples 2 and 3 were dissolved in a 6N-hydrochloric acid solution, respectively, to prepare a mixed solution (100 ml) of MgCl2 + FeCl3 (Mg/Fe molar ratio = 1.99) and a mixed solution (100m1) of MgCl2 + A1C13 (Mg/A1 molar ratio =
2.15). The mixed solutions were boiled to remove carbon dioxide. Metal hydroxide complexes C1/HT-Fe (Mg2+0.651Fe3+0.349(OH )2.18301 0.090(0032 )0.038 and C1/HT-A1 (Mg2~0.676A13+0.324(OH )2.08201 0.214(0032 )0.014) were then prepared according to a method described by Langmuir, 9, 1418-1422 (1993). The adsorbed amounts of phosphorus determined in the same manner as example 1 are 0.97 mmolP/g with respect to Cl/HT-Fe and 2.13 mmolP/g with respect to C1/HT-A1, respectively.
Example 7 The metal oxide complexes (1 g) obtained in example 3 were added to a Na2HP04 aqueous solution (80cm3) having a phosphate concentration of 26.7 mM-P, and the mixtures was stirred at 25 °C for 4 hours, respectively. After stirring, each phosphate adsorbent was filtered off. Phosphate ion concentrations of filtrates determined in the same manner as example 1 are 1.00 mmolP/g with respect to MgFeO and 0.87 mmolP/g with respect to MgAlO.
For the purpose of desorption of phosphate, 0.3 g of phosphate-containing phosphate adsorbents thus ' -23-obtained (hereinafter referred to as "P/MgFeO" and "P/MgAlO") were added to 2M-Na2C03 aqueous solution (24cm3), respectively, to exchange phosphate ion for carbonate ion. After stirring at 90 °C for 2 hours, each phosphate adsorbent was filtered off. After washing with water, drying and dissolving in hydrochloric acid solution, phosphate ion concentrations of the filtrates were determined in the same manner as example 1 to calculate the remaining phosphorus in the phosphate adsorbents. With respect to P/MgFeO and P/MgAlO, the remaining phosphorus are determined as O.lOmmolP/g and 0.47 mmolP/g, respectively, indicating that phosphorus of P/MgFeO was desorbed about 90 %, and that phosphorus of P/MgAlO was desorbed about 46 %. The phosphate adsorbent powders after phosphate desorption treatment were subjected to X-ray diffraction analysis. The results of the analysis demonstrate that C03/HT-Fe and C03/HT-A1 structures are regenerated. The regenerated phosphate adsorbents may be used according to the methods of examples 3, 4 or 6.
Example 8 A 0.01 g of phosphate adsorbent, C1/HT-Fe or C1/HT-A1 was added to model waste water (40 ml) containing a variety of ions (2.0 ppm-P; 10.4 ppm-N02 ;
7.0 ppm-N03 ; and 16.5 ppm-S042 ). The mixture was stirred at room temperature for 4 hours. After stirring, the phosphate adsorbent was filtered off. A phosphate ion concentration in the filtrate was determined in the same manner as example 1, and other ions in the filtrate were determined by ion chromatography. The results are shown in table 1. Table 1 demonstrates that not only phosphate but also other ions are significantly reduced by treating the model waste water with the phosphate adsorbents.
Table 1 Agent for treating Ion concentration (ppm).
waste water P N02- N03- S04-_ C1/HT-Fe 0.7 2.9 1.5 12.1 C1/HT-A1 0.2 2.4 1.1 8.0 Example 9 A 0.5 g of the phosphate-containing phosphate adsorbent (P/HT-A1) was added to an Erlenmeyer flask with ground stopper to which a 6 % NaOH + 30% NaCl mixed solution (20 ml) was added. The mixture was shaked laterally (170 shake/min) for 4 hours. The phosphate adsorbent was filtered~off and the agent was washed with water. The phosphate adsorbent was subjected to the shaking treatment as above using 79.3 % MgCl2 aqueous solution. The amount of desorbed phosphate ion was calculated as adsorption per 1 g of the phosphate adsorbent by determining a phosphate concentration of the filtrate according to the method of example 1. The desorbed amount of phosphorus is 1.73 mmolP/g.
Example 10 -- The desorbed amount of phosphorus is determined in the same manner as example 9 except that the phosphate adsorbent was treated with 3% NaOH aqueous solution and 79.3 % MgCl2 aqueous solution in this sequence as solution for desorption.
The desorbed amount of phosphorus is 1.50 mmolP/g.
Example 11 The regenerated phosphate adsorbents obtained in examples 9 and 10 were treated in the same manner as example 1 to determine the adsorbed amount of phosphorus.
The adsorbed amounts of phosphorus are 1.79 mmolP/g (example 9) and 1.65 mmolP/g (example 10). The regeneration percents of phosphate adsorbents are as high as 84% and 77% based on the saturated phosphorus adsorption of the phosphate adsorbent C1/HT-A1, 2.13 mmolP/g.
Example 12 A suitable amount of polyacrylic hydrazide and polyamide/epichlorohydrin resin as a binder were added to 4 kg of phosphate adsorbent (Cl/HT-A1). The resulting mixture was kneaded with a kneader (output = 1.5 kw;
total volume = 20 liter; binary shaft number of revolution = 29.20 rpm) under conditions of mixing time between phosphate adsorbent and binder (= 1 minute) and kneading time after adding a required amount of water (_ 5 minutes). Granulates (diameter = 3 mm; length = 5-10 mm) were prepared with upstroke-type extrusion granulators (output = 3.7 kw; screen = 3 mm ; number of revolution = 135 rpm), and the granulates were dried at 80 °C for 15 hours.
Example 13 The granulates obtained in example 12 were subjected to a strength test and a phosphate-adsorption test. The strength test was carried out according to the following procedure. A 1.0 g of accurately weighed granulates and 20 ml of water were added to an Erlenmeyer flask with ground stopper. The flask was shaked with lateral-shake thermostat at 30°C, 170 shake/min for 3 hours. After filtration and drying, a total weight of the granulates were determined. The resulting granulates were sieved with 10-mesh sieve to weigh residue on sieve and sieve-passed fraction. Lrushing resistance strength (L) is calculated by the following equation.
Crushing resistance strength = 100 - {P/(S + P)~ x 100 wherein P = weight of 10-mesh sieve-passed fraction; and S = weight of residue on 10-mesh sieve. Crushing resistance strength is practically needed 85 or more.
The phosphate adsorption test was conducted according to the following procedure.
A 1.0 g of granulates was accurately weighed and added to an Erlenmeyer flask with ground stopper. A
20 ml of the aqueous solution of Na2HP04 used in example 1 was added thereto. The flask was laterally shaked at 30°C,_170 shake/min for 3 hours. After filtration, a phosphate concentration of the filtrate was determined in the same manner as example 1 to calculate the amount of phosphate adsorbed. The results were shown in table 2.
Table 2 Binder Loading Capacity Adsorbed Crushing of of binder granulator phosphate resistance (wt.%) (kq/hr) (mmolP/q) stren t~ h Poly-acrylic 1.0 70 0.69 86.4 h~drazide Poly-acrylic 3.0 60 0.60 99.5 hydrazide Polyamide epichloro- 5.0 150 1.28 33.5 hydrine resin Poly-acrylic 1.0 hydrazide Polyamide 110 0.67 97.3 epichloro-hydrine 4.0 resin The results of table 2 show that the phosphate adsorbent of the invention meets the waste water quality standard with respect to a septic tank, sewerage, waste water from village. The phosphate adsorbent of the invention will be applicable to the more strict standard.
Example 14 The granulates obtained in example 12 were ground. A predetermined amount of the ground product (particle size : 200-280 mesh) was added to an aqueous NaH2P04 solution (2,000 ml, pH=6.8) adjusted to a phosphorous concentration of lppm-P, and the resulting mixture was stirred at 25 °C so as to determine the change of a phosphorous concentration relative to a stirring time. Determmination of the phosphorous concentration were carried out in the same manner as example 1. The results are shown in fig.3. Fig.3 shows that a rate of phosphate adsorption increases with the increase of the added amount of the ground product and that phosphate was removed and adsorbed withis 10 minutes from the addition of the phosphate adsorbent (0.025 %) thereto.
Example 15 Phosphate adsorption capacity of a phosphate adsorbent was evaluated using waste water with a low phosphate concentration. The waste water was collected from an equipment for waste water treatment located in a farm area in KASHIMA-cho, SHIMANE-ken JAPAN. The phasphate adsorbent (C1/HT-Al, O.lg) was added to the waste water (400 ml). The resulting mixture was strred with a magnetic stirrer for 4 hours. After stirring, the treated water was filtered with a 0.45um-membrane filter to analyze the phosphate concentration of the filtrate according to the assay method defined by Japanese ,Industrial Standard (JIS). The phosphate concentration of the waste water (0.18 ppm-P) was decreased by the treatment below detection limit of phosphate showing usefulness of the phosphate adsobent of the invention when applied to waste water with low phosphate concentration.
Claims (10)
1. A method for treating phosphate-containing waste water comprising treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1):
M1-x2+M x3+(OH)~2+x-y(A n-)y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+; Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of Al3+ and Fe3+, A n- represents n-valent anion, 0.1<=x<=0.5, 0.1<=y<=0.5 and n is 1 or 2 to adsorb phosphate.
M1-x2+M x3+(OH)~2+x-y(A n-)y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+; Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of Al3+ and Fe3+, A n- represents n-valent anion, 0.1<=x<=0.5, 0.1<=y<=0.5 and n is 1 or 2 to adsorb phosphate.
2. A method for treating phosphate-containing waste water according to claim 1 comprising the steps of:
step (I) : treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) :
M1-x2+M x3+(OH~)2+x-y(A n-)y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of Al3+ and Fe3+, An represents n-valent anion, 0.1<=x<=0.5, 0.1<=y<=0.5 and n is 1 or 2 to adsorb phosphate; and step (II) : treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with at least one phosphate-desorbing agent selected from the group consisting of alkaline metal salts and alkaline earth metal salts other than alkaline metal carbonates and alkaline earth metal carbonates to regenerate and recycle the phosphate adsorbent.
step (I) : treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) :
M1-x2+M x3+(OH~)2+x-y(A n-)y/n (1) wherein M2+ represents at least one divalent metal ion selected from the group consisting of Mg2+, Ni2+, Zn2+, Fe2+, Ca2+ and Cu2+, M3+ represents at least one trivalent metal ion selected from the group consisting of Al3+ and Fe3+, An represents n-valent anion, 0.1<=x<=0.5, 0.1<=y<=0.5 and n is 1 or 2 to adsorb phosphate; and step (II) : treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with at least one phosphate-desorbing agent selected from the group consisting of alkaline metal salts and alkaline earth metal salts other than alkaline metal carbonates and alkaline earth metal carbonates to regenerate and recycle the phosphate adsorbent.
3. A method for treating phosphate-containing waste water according to claim 1 comprising the steps of:
step (I) : treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) :
M1-x2+M x3+(OH~)2+x-y(A n-)y/n (1) wherein M2+, M3+, A n-, x, y and n are as defined above.
to adsorb phosphate;
step (Ia) : treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with an aqueous solution containing an alkaline metal carbonate or A n- ion to desorbing and recovering phosphates;
step (Ib) : calcinating the phosphate adsorbent after dephosphorization of step (Ia) at about 430-600 °C;
step (II) : treating the phosphate adsorbent after calcination with at least one phosphate-desorbing agent selected from the group consisting of alkaline metal salts and alkaline earth metal salts other than alkaline metal carbonates and alkaline earth metal carbonates to regenerate and recycle the phosphate adsorbent.
step (I) : treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) :
M1-x2+M x3+(OH~)2+x-y(A n-)y/n (1) wherein M2+, M3+, A n-, x, y and n are as defined above.
to adsorb phosphate;
step (Ia) : treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with an aqueous solution containing an alkaline metal carbonate or A n- ion to desorbing and recovering phosphates;
step (Ib) : calcinating the phosphate adsorbent after dephosphorization of step (Ia) at about 430-600 °C;
step (II) : treating the phosphate adsorbent after calcination with at least one phosphate-desorbing agent selected from the group consisting of alkaline metal salts and alkaline earth metal salts other than alkaline metal carbonates and alkaline earth metal carbonates to regenerate and recycle the phosphate adsorbent.
4. A method for treating phosphate-containing waste water according to claim 1 comprising the steps of:
step (I) : treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) :
M1-x2+M x3+(OH-)2+x-y(An-)y/n (1) wherein M2+, M3+, A n-, x, y and n are as defined above.
to adsorb phosphate;
step (Ia) : treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with an aqueous solution containing an alkaline metal carbonate or A n- ion to desorb and recover phosphates;
step (Ic) : dissolving the phosphate-desorbed phosphate adsorbent in an acidic solution to recycle the solution as raw material for producing a phosphate adsorbent.
step (I) : treating phosphate-containing waste water with a metal hydroxide complex as a phosphate adsorbent represented by formula (1) :
M1-x2+M x3+(OH-)2+x-y(An-)y/n (1) wherein M2+, M3+, A n-, x, y and n are as defined above.
to adsorb phosphate;
step (Ia) : treating the phosphate-adsorbed phosphate adsorbent obtained in step (I) with an aqueous solution containing an alkaline metal carbonate or A n- ion to desorb and recover phosphates;
step (Ic) : dissolving the phosphate-desorbed phosphate adsorbent in an acidic solution to recycle the solution as raw material for producing a phosphate adsorbent.
5. A method for treating phosphate-containing waste water according to claim 1 comprising the steps of:
step (III) : treating the calcinated phosphate adsorbent obtained in step (Ib) of claim 3 with phosphate-containing waste water; and step (IV) : repeating step (II) of claim 2 or steps (Ia), (Ib) and (II) of claim 3 using the phosphate-adsorbed phosphate adsorbent obtained in step (III).
step (III) : treating the calcinated phosphate adsorbent obtained in step (Ib) of claim 3 with phosphate-containing waste water; and step (IV) : repeating step (II) of claim 2 or steps (Ia), (Ib) and (II) of claim 3 using the phosphate-adsorbed phosphate adsorbent obtained in step (III).
6. A method for treating phosphate-containing waste water according to claim 1 comprising dissolving the calcinated phosphate adsorbent obtained in step (Ib) of claim 3 in an acidic solution to recycle the solution as raw material for producing a phosphate adsorbent.
7. An agent for removing phosphates, nitrates and nitrites from waste water comprising a metal hydroxide complex as a phosphate adsorbent represented by formula (1) :
M1-x2+M x3+(OH-)2+x-y(A n-)y/n (1) wherein M2+, M3+, A n-, x, y and n are as defined above.
M1-x2+M x3+(OH-)2+x-y(A n-)y/n (1) wherein M2+, M3+, A n-, x, y and n are as defined above.
8. A granulate of phosphate adsorbent for treating phosphate-containing waste water comprising about 99-60 % by weight of a metal hydroxide complex as a phosphate adsorbent represented by formula (1) :
M1-x2+M x3+(OH-)2+x-y(A n-)y/n (1) wherein M2+, M3+, A n-, x, y and n are as defined above and about 1-40 % by weight of binder.
M1-x2+M x3+(OH-)2+x-y(A n-)y/n (1) wherein M2+, M3+, A n-, x, y and n are as defined above and about 1-40 % by weight of binder.
9. The granulate according to claim 8 wherein said binder comprises an aminated polyacrylamide.
10. The granulate according to claim 8 wherein said-binder comprises about 99-60 % by weight of an aminated polyacrylamide and about 1-40 % by weight of at least one selected from the group consisting of polyamide/epichlorohydrin resin, vinyl acetate/vinyl versate copolymer resin and styrene/acryl resin.
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP208079/1996 | 1996-08-07 | ||
| JP20807996 | 1996-08-07 | ||
| JP29899996 | 1996-11-11 | ||
| JP298999/1996 | 1996-11-11 | ||
| JP15527697 | 1997-06-12 | ||
| JP155276/1997 | 1997-06-12 |
Publications (2)
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| CA2212405A1 CA2212405A1 (en) | 1998-02-07 |
| CA2212405C true CA2212405C (en) | 2005-05-10 |
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|---|---|---|---|
| CA002212405A Expired - Fee Related CA2212405C (en) | 1996-08-07 | 1997-08-06 | Method for treating waste water |
Country Status (4)
| Country | Link |
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| US (2) | US5976401A (en) |
| EP (2) | EP0823401B1 (en) |
| CA (1) | CA2212405C (en) |
| DE (1) | DE69725794T9 (en) |
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| DE19723212C2 (en) * | 1997-06-03 | 2000-01-27 | Bk Giulini Chem Gmbh & Co Ohg | Process for the treatment of waste water to improve denitrification with simultaneous dephosphation by additives |
| DE19743606A1 (en) * | 1997-10-02 | 1999-04-15 | Hydro Agri Deutschland Gmbh | Use of anion-exchanging minerals |
| RU2179954C1 (en) | 2000-06-22 | 2002-02-27 | Стремилова Нина Николаевна | Composition for treatment of natural water and waste waters and a method for preparing composition for treatment of natural and waste waters |
| AU2002345915A1 (en) * | 2001-06-25 | 2003-01-08 | Eda, Inc. | Compositions and methods for anion adsorbent metal hydroxides |
| US20050107253A1 (en) * | 2001-12-21 | 2005-05-19 | Hiroyuki Sano | Adsorbent for phosphoric acid |
| AU2003289540A1 (en) * | 2002-12-31 | 2004-07-22 | Ku-Su Kim | Wastewater disposal agent and process for preparing thereof |
| US7135156B2 (en) * | 2003-03-28 | 2006-11-14 | Baxter International Inc. | Method for processing a zirconium oxide composition in crystalline form |
| AU2003903646A0 (en) * | 2003-07-16 | 2003-07-31 | Bushwater Holdings Pty Ltd | Waste water treatment |
| AU2004257891B2 (en) * | 2003-07-16 | 2010-03-04 | Magnesium Tech Pty Ltd | Waste water treatment |
| TW200518137A (en) * | 2003-08-13 | 2005-06-01 | Showa Denko Kk | Chip solid electrolyte capacitor and production method of the same |
| US7311844B1 (en) * | 2006-06-22 | 2007-12-25 | Joyner Bobby L | Method of treating stormwater runoff and domestic waste with coal ash |
| AU2008322276A1 (en) * | 2007-11-12 | 2009-05-22 | Technion Research And Development Foundation Ltd. | Method for adsorption of phosphate contaminants from water solutions and its recovery |
| MX2010011415A (en) * | 2008-04-16 | 2011-04-07 | William Lucas | Bioretention system and method. |
| US7588744B1 (en) * | 2008-12-08 | 2009-09-15 | Layne Christensen Company | Method of recovering phosphate for reuse as a fertilizer |
| WO2010122509A2 (en) * | 2009-04-21 | 2010-10-28 | Ecolab Usa Inc. | Methods and apparatus for controlling water hardness |
| US9193610B2 (en) | 2011-08-10 | 2015-11-24 | Ecolab USA, Inc. | Synergistic interaction of weak cation exchange resin and magnesium oxide |
| CN103241795A (en) * | 2013-05-17 | 2013-08-14 | 南京理工大学 | Method for removing phosphorus pollutants in sewage |
| CN106215849A (en) * | 2015-06-24 | 2016-12-14 | 中国环境科学研究院 | The preparation method of a kind of many metal hydroxidess efficient dephosphorization agent and purposes |
| US10517893B2 (en) * | 2017-08-25 | 2019-12-31 | Changhua Christian Medical Foundation Changhua Christian Hospital | Cationic binder, pharmaceutical composition comprising the same and method of using the same |
| CN108525647A (en) * | 2018-04-12 | 2018-09-14 | 华东交通大学 | Biomass carbon/copper magnalium ternary metal hydroxide denitrogenates phosphate material preparation method |
| CN109987691A (en) * | 2019-04-23 | 2019-07-09 | 宁夏佳仕德水处理科技有限公司 | A kind of efficient dephosphorization agent for sewage treatment |
| CN110498532A (en) * | 2019-08-15 | 2019-11-26 | 深南电路股份有限公司 | The processing method and processing unit of printed wiring board waste water |
| CN111874984B (en) * | 2020-07-28 | 2022-08-23 | 上海泽耀环保科技有限公司 | Water body restoration rope and preparation method and application thereof |
| CN113083258A (en) * | 2021-04-19 | 2021-07-09 | 临沂海普新材料科技有限公司 | Preparation method of heavy metal-containing high-salinity wastewater recycling adsorbent |
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| US3002932A (en) * | 1958-10-27 | 1961-10-03 | Minnesota Mining & Mfg | Inorganic anion-exchangers and a process for their preparation |
| US3063807A (en) * | 1960-02-23 | 1962-11-13 | Glidden Co | Purification of water-insoluble solids by ion exchange |
| EP0022475A1 (en) * | 1979-07-06 | 1981-01-21 | Allied Corporation | Aqueous basic polyaluminum-iron halide solutions and method of preparing |
| CA1180827A (en) * | 1982-03-23 | 1985-01-08 | Michael Heskins | Polymeric flocculants |
| JPS60161744A (en) * | 1984-01-30 | 1985-08-23 | Kyowa Chem Ind Co Ltd | Purification agent and method for cooling water of atomic power plant |
| JPS6164388A (en) * | 1984-09-05 | 1986-04-02 | Kohei Urano | Removal of phosphorus in water |
| GR862353B (en) * | 1985-09-23 | 1987-01-19 | Lilly Co Eli | Anti-tumor method and compounds |
| DE3838532A1 (en) * | 1988-11-14 | 1990-05-17 | Henkel Kgaa | CLAIMS OR FLAKES FOR WASTEWATER TREATMENT AND METHOD USING THIS MEANS |
| US4935146A (en) * | 1988-11-15 | 1990-06-19 | Aluminum Company Of America | Method for removing arsenic or selenium from an aqueous solution containing a substantial background of another contaminant |
| DE4018628A1 (en) * | 1990-06-11 | 1991-12-12 | Henkel Kgaa | COAGULATORS BASED ON DOUBLE LAYER HYDROXIDE COMPOUNDS |
| DE19651135A1 (en) * | 1996-12-10 | 1998-06-18 | Kruse Chemie Kg | Precipitating agent for treating water or effluent to remove phosphate(s), etc. |
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- 1997-08-06 EP EP97113595A patent/EP0823401B1/en not_active Expired - Lifetime
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| EP0823401A2 (en) | 1998-02-11 |
| EP0823401B1 (en) | 2003-10-29 |
| CA2212405A1 (en) | 1998-02-07 |
| DE69725794T2 (en) | 2004-08-12 |
| US5976401A (en) | 1999-11-02 |
| DE69725794T9 (en) | 2004-12-16 |
| EP0823401A3 (en) | 1998-03-18 |
| EP1342697A3 (en) | 2004-05-06 |
| DE69725794D1 (en) | 2003-12-04 |
| EP1342697A2 (en) | 2003-09-10 |
| US6132624A (en) | 2000-10-17 |
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