JPS601069B2 - Method for removing phosphates from wastewater - Google Patents
Method for removing phosphates from wastewaterInfo
- Publication number
- JPS601069B2 JPS601069B2 JP17969980A JP17969980A JPS601069B2 JP S601069 B2 JPS601069 B2 JP S601069B2 JP 17969980 A JP17969980 A JP 17969980A JP 17969980 A JP17969980 A JP 17969980A JP S601069 B2 JPS601069 B2 JP S601069B2
- Authority
- JP
- Japan
- Prior art keywords
- wastewater
- phosphates
- coral
- fossils
- calcined
- 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
Links
- 229910019142 PO4 Inorganic materials 0.000 title claims description 13
- 235000021317 phosphate Nutrition 0.000 title claims description 13
- 239000002351 wastewater Substances 0.000 title claims description 13
- 150000003013 phosphoric acid derivatives Chemical class 0.000 title claims description 12
- 238000000034 method Methods 0.000 title claims description 10
- 235000014653 Carica parviflora Nutrition 0.000 claims description 21
- 241000243321 Cnidaria Species 0.000 claims description 20
- 150000003839 salts Chemical class 0.000 claims description 3
- 238000010304 firing Methods 0.000 claims description 2
- 238000001179 sorption measurement Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000011575 calcium Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 241000242757 Anthozoa Species 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000630665 Hada Species 0.000 description 1
- 241000237852 Mollusca Species 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical class [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
Landscapes
- Removal Of Specific Substances (AREA)
- Water Treatment By Sorption (AREA)
Description
【発明の詳細な説明】
本発明は、焼成サンゴ化石をリン酸塩類含有廃水の処理
剤として使用する廃水中のリン酸塩類除去方法に関する
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for removing phosphates from wastewater using calcined coral fossils as a treatment agent for phosphate-containing wastewater.
琉球列島付近には、サンゴ礁の産地を控えており、その
採掘可能な埋蔵量は5批富トンと推定され豊富な資源と
して有効利用が期待されている。There are coral reef producing areas near the Ryukyu Islands, and the mineable reserves are estimated to be 5 tons, and it is expected that they will be put to effective use as a rich resource.
サンゴ化石は方解石を主成分とし、若干の霧石を含有し
ているもので、第4紀の地質時代のサンゴ、有孔虫石灰
藻、軟体動物遺骸から構成されたもので非常に多孔質の
化石である。サンゴ化石の化学分析の一例を示せば次の
第1表のようである。第1表惨腰P205 肌 舷2。Coral fossils are mainly composed of calcite and contain some mist, and are composed of corals, foraminiferal calcareous algae, and mollusk remains from the Quaternary geological period, and are extremely porous. It is a fossil. An example of chemical analysis of coral fossils is shown in Table 1 below. Table 1: Menkoshi P205 Hada Gunma 2.
3Fe203 Ca。3Fe203Ca.
MgOS。8 Na20K20計47.7 0.6
7 2.2 1.2 0.4 53
.2 1.2 0.3 0.17 0.07
100本出願人は、豊富なサンゴ化石を焼成し、廃水中
の重金属類の除去剤とする研究開発中、廃水中のリン酸
塩類の除去剤としても使用できるのではないかと研究中
、有効に使用できることを見出し本発明を完成するに到
った。MgOS. 8 Na20K20 total 47.7 0.6
7 2.2 1.2 0.4 53
.. 2 1.2 0.3 0.17 0.07
100 The applicant is currently researching and developing the use of calcined coral fossils as a remover for heavy metals in wastewater, and is researching whether it can also be used as a remover for phosphates in wastewater. They found that it can be used and completed the present invention.
従来、リン酸塩類を含有する廃水の処理には石灰を用い
リン酸カルシウムの塩類として沈降せしめ除去するのが
普通である。Conventionally, in the treatment of wastewater containing phosphates, it has been common to use lime to precipitate and remove calcium phosphate salts.
リン酸のカルシウム塩はアルカリ塩よりも水に対する熔
解度が小であるから沈降除去できるが、カルシウム塩が
有する溶解度に相当する量は少なくとも廃水中に残留す
る。又沈降し難い沈殿物を生じ浮遊する欠点がある。実
質的完全に廃水中のリン酸塩類を除去するためには、吸
着剤、例えば活性炭を用いて吸着除去することができる
が活性炭は高価であるのが欠点である。Since calcium salts of phosphoric acid have lower solubility in water than alkaline salts, they can be removed by sedimentation, but at least an amount corresponding to the solubility of the calcium salts remains in the wastewater. It also has the disadvantage of forming a precipitate that is difficult to settle and floating. In order to substantially completely remove phosphates from wastewater, adsorbents such as activated carbon can be used to remove them by adsorption, but activated carbon is expensive.
石灰で中和しても残留する少量のリン酸塩類を除去する
安価な除去剤を使用する方法が業界では要望されている
。There is a need in the industry for an inexpensive removal agent that removes the small amounts of phosphates that remain after neutralization with lime.
この要望に応えて安価なリン酸塩類の除去法を提供する
のが本発明の目的である。本発明は、実質的に塩分を含
有しないサンゴ化石を300〜500ooで焼成し、リ
ン酸塩を含有する廃水の処理剤として使用することを特
徴とする廃水中のリン酸塩除去方法、を提供する。It is an object of the present invention to provide an inexpensive method for removing phosphates in response to this demand. The present invention provides a method for removing phosphates from wastewater, which comprises burning coral fossils that do not substantially contain salt at a temperature of 300 to 500 oo and using the resultant as a treatment agent for wastewater containing phosphates. do.
サンゴ化石の焼成には、サンゴ化石を水、好ましくは温
湯にて洗浄し塩分を除去した後、300〜500℃にお
いて焼成し、冷却後使用条件に適応した大きさに粉砕し
て使用する。For firing coral fossils, the coral fossils are washed with water, preferably hot water to remove salt, then fired at 300 to 500°C, cooled, and then crushed into a size suitable for usage conditions.
塔に充填して使用する場合と櫨杵機付の糟で鷹洋混合し
て使用する場合により粒の大きさを変えることが好まし
い「使用目的に従って粒度を決めることができる。30
000以下で焼成したサンゴ化石は吸着館が弱い。It is preferable to change the particle size depending on whether it is used packed in a tower or mixed in a kettle with a pestle.The particle size can be determined according to the purpose of use.30
Coral fossils fired below 0.000 have weak adsorption capacity.
50000以上で焼成したサンゴ化石はその吸着能が低
下する。実施例 1
焼成サンゴ化石粒度250〜840仏mのものを試験液
500のとに対し10,25,50g使用した。Coral fossils fired at a temperature of 50,000 or more have a reduced adsorption capacity. Example 1 10, 25, and 50 g of calcined coral fossil particles having a particle size of 250 to 840 French m were used for 500 test liquids.
試験液としてはリン酸三ナトリウム(Na3P04・1
2日20)をP04として30ppmを目標にpHは2
.5として調整した。処理槽の鷹梓時間は1,2,5,
7の4条件とした。使用原液濃度 P0430.7pp
m Na24.5ppmS0417のpmで分析方法と
しては次の方法に従った。The test solution was trisodium phosphate (Na3P04.1
2nd day 20) as P04 and the pH is 2 with a target of 30 ppm.
.. Adjusted as 5. Takaazusa time of treatment tank is 1, 2, 5,
7.4 conditions were set. Concentration of stock solution used P0430.7pp
mNa24.5ppmS0417 pmThe following method was followed as an analysis method.
P04・…・・吸光光度法
Ca・・・・・・原子吸光法
Na・・・…原子吸光法
S04・・・・・・重量法
焼成サンゴ化石(除去剤)の使用量、処理後の液のpH
、変化、蝿梓時間と除去処理後のロ液中に残留するP0
4,Ca,Na,S04の相互関係を第2表に示す。P04... Spectrophotometry Ca... Atomic absorption method Na... Atomic absorption method S04... Gravimetric method Amount of burned coral fossil (removal agent) used, liquid after treatment pH of
, Changes, P0 remaining in the filtrate after removal treatment
Table 2 shows the interrelationships among 4, Ca, Na, and S04.
第2表 焼成サンゴ化石除去剤による除去率(バッチ式
)実施例 2実施例1と同じ粒度の焼成サンゴ化石をカ
ラムに充填して760〜800の【/hの流速で通液時
間1,2,3,4,5,6,7時間、原液濃度P04・
・・30.5ppmNa・・・21.2ppmS04・
・・163.4ppmの液を用いた場合の除去率を第3
表に示す。Table 2 Removal rate by calcined coral fossil remover (batch type) Example 2 Calcined coral fossils with the same particle size as in Example 1 were packed into a column, and the liquid flow time was 1,2 at a flow rate of 760 to 800 [/h]. , 3, 4, 5, 6, 7 hours, stock solution concentration P04・
・・30.5ppmNa・・21.2ppmS04・
...3rd removal rate when using 163.4 ppm solution
Shown in the table.
第3表 焼成サンゴ化石除去剤による除去率(コラム式
)使用済の焼成サンゴ化石のX線回析の結果P04は吸
着の外Caと化合物を形成していることが確認された。Table 3: Removal rate by calcined coral fossil remover (column type) As a result of X-ray diffraction of used calcined coral fossils, it was confirmed that P04 forms a compound with Ca in addition to adsorption.
本発明の焼成サンゴ化石のP04の吸着能を見るため、
P04として10,000ppmの濃度の液500肌に
焼成サンゴ化石5gを添加し5時間蝿拝した結果170
肌g/5g、すなわち340/gの吸着除去能力を有す
ることを確認した。比較例
実施例に従って、焼成しないサンゴ化石を廃水中のリン
酸塩類の除去に使用できるかを試験したが、全く除去で
きなかった。In order to check the P04 adsorption ability of the calcined coral fossil of the present invention,
As P04, 5g of calcined coral fossil was added to 500 skins with a concentration of 10,000ppm, and the result was 170 after 5 hours of worshiping.
It was confirmed that it had an adsorption removal ability of skin g/5g, that is, 340/g. Comparative Example A test was conducted to see if uncalcined coral fossils could be used to remove phosphates from wastewater in accordance with the example, but no removal was possible.
Claims (1)
00℃で焼成し、リン酸塩を含有する廃水の処理剤とし
て使用することを特徴とする廃水中のリン酸塩除去方法
。1 300 to 5 coral fossils containing virtually no salt
A method for removing phosphates from wastewater, which comprises firing at 00°C and using the process as a treatment agent for wastewater containing phosphates.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17969980A JPS601069B2 (en) | 1980-12-20 | 1980-12-20 | Method for removing phosphates from wastewater |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17969980A JPS601069B2 (en) | 1980-12-20 | 1980-12-20 | Method for removing phosphates from wastewater |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57105281A JPS57105281A (en) | 1982-06-30 |
| JPS601069B2 true JPS601069B2 (en) | 1985-01-11 |
Family
ID=16070321
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17969980A Expired JPS601069B2 (en) | 1980-12-20 | 1980-12-20 | Method for removing phosphates from wastewater |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS601069B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0677732B2 (en) * | 1986-07-29 | 1994-10-05 | 新鉱工業株式会社 | Adsorbent for water treatment and method for producing the same |
| JPH0330894A (en) * | 1989-06-29 | 1991-02-08 | Shimizu Corp | Method for preventing contamination of lake and marsh and reservoir |
-
1980
- 1980-12-20 JP JP17969980A patent/JPS601069B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57105281A (en) | 1982-06-30 |
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