JPH0533081B2 - - Google Patents
Info
- Publication number
- JPH0533081B2 JPH0533081B2 JP6507884A JP6507884A JPH0533081B2 JP H0533081 B2 JPH0533081 B2 JP H0533081B2 JP 6507884 A JP6507884 A JP 6507884A JP 6507884 A JP6507884 A JP 6507884A JP H0533081 B2 JPH0533081 B2 JP H0533081B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- treatment
- rock
- turbidity
- treatment agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000011282 treatment Methods 0.000 claims description 94
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 87
- 239000003795 chemical substances by application Substances 0.000 claims description 69
- 238000000034 method Methods 0.000 claims description 37
- 239000011435 rock Substances 0.000 claims description 37
- 239000002245 particle Substances 0.000 claims description 32
- 239000000843 powder Substances 0.000 claims description 17
- 238000005352 clarification Methods 0.000 claims description 13
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 10
- 238000003756 stirring Methods 0.000 claims description 10
- 239000008394 flocculating agent Substances 0.000 claims description 9
- 229910052655 plagioclase feldspar Inorganic materials 0.000 claims description 6
- 239000010433 feldspar Substances 0.000 claims description 4
- 239000002244 precipitate Substances 0.000 claims description 4
- 239000008262 pumice Substances 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 229910021578 Iron(III) chloride Inorganic materials 0.000 claims description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims description 2
- 239000011790 ferrous sulphate Substances 0.000 claims description 2
- 235000003891 ferrous sulphate Nutrition 0.000 claims description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims description 2
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims description 2
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 claims description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 claims description 2
- 229910000360 iron(III) sulfate Inorganic materials 0.000 claims description 2
- 239000002178 crystalline material Substances 0.000 claims 1
- 239000000047 product Substances 0.000 description 20
- 238000012545 processing Methods 0.000 description 19
- 230000000694 effects Effects 0.000 description 15
- 238000012360 testing method Methods 0.000 description 13
- 239000007788 liquid Substances 0.000 description 12
- 238000004062 sedimentation Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 238000007796 conventional method Methods 0.000 description 9
- 239000003344 environmental pollutant Substances 0.000 description 7
- 238000002347 injection Methods 0.000 description 7
- 239000007924 injection Substances 0.000 description 7
- 231100000719 pollutant Toxicity 0.000 description 7
- 238000001179 sorption measurement Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 230000002776 aggregation Effects 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 238000005189 flocculation Methods 0.000 description 5
- 230000016615 flocculation Effects 0.000 description 5
- 239000010842 industrial wastewater Substances 0.000 description 5
- 238000010998 test method Methods 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 230000015271 coagulation Effects 0.000 description 4
- 238000005345 coagulation Methods 0.000 description 4
- 239000005416 organic matter Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000006228 supernatant Substances 0.000 description 4
- 239000002351 wastewater Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000005054 agglomeration Methods 0.000 description 3
- 239000000356 contaminant Substances 0.000 description 3
- 239000003673 groundwater Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000004220 aggregation Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000701 coagulant Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 244000144992 flock Species 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- CCEKAJIANROZEO-UHFFFAOYSA-N sulfluramid Chemical group CCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F CCEKAJIANROZEO-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000001994 activation Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910052650 alkali feldspar Inorganic materials 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 235000012206 bottled water Nutrition 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000002925 chemical effect Effects 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000010840 domestic wastewater Substances 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000008235 industrial water Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229910001562 pearlite Inorganic materials 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000010801 sewage sludge Substances 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000003206 sterilizing agent Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000002352 surface water Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Description
(3‐1) 産業上の利用分野
本発明は汚濁水を高速に清澄化する処理方法に
係り、詳細には、〓紋岩、真珠岩、泥溶岩等玻璃
質に長石(斜長石、アルカリ長石)を含む火成岩
(以下単に「〓紋岩等」ということにする。)の微
粉と、〓紋岩質浮岩堆積岩、浮石質凝灰岩等玻璃
質に斜長石を含む浮岩質堆積岩(以下単に「浮岩
質堆積岩」というときはこれを指すことにする。)
微粉とを配合した微粉剤とアルミニウム塩等の無
機凝集剤とを同時に汚濁水に注入することによつ
て汚濁成分の凝集沈降を従来法に較べて格段に効
率化した汚濁水の高速清澄処理法に関する。
(3‐2) 従来技術
濁質を含む水を処理する場合としては、上水、
工業用水の浄化処理、病院、学校、ホテル、厨
房、産業排水等の生活排水の処理、食品、染色、
化学、薬品工業排水等の工業排水の処理等が考え
られるが、いずれの場合にも、篩分槽、沈澱槽、
ろ過槽等の設備を設置し、その設備において適
宜、吸着、凝集、活性化等の処理操作を行うこと
によつて清澄化が行なわれている。
たとえば上水の浄化処理においては、塩素によ
るマンガン、鉄の化学的分離または滅菌処理、ポ
リ塩化アルミニウム、硫酸アルミニウム、塩化鉄
等の凝集剤と、消石灰、ソーダ灰等の凝集助剤に
よる沈澱等重力利用の物理的、化学的処理、汚
泥、活性菌による生物学的処理、等を適宜組合わ
せることによつて処理が行なわれている。しかし
ながらこれ等の汚濁水を処理する従来の処理法に
おいてはいずれも大型の処理設備が必要で、大き
な設備費と、設置場所を必要とし、また処理には
かなり時間を必要とする欠点があつた。
(3‐3) 発明の目的
本発明は汚濁水を清澄化する従来の処理法の以
上述べた欠点を改善し、大型の処理設備を必要と
せず容易にしかも極めて短時間に汚濁水を清澄化
する処理法を提供し、併せて災害時等における緊
急用水確保のための簡便な方法を提供することを
目的としている。
(3‐4) 発明の構成・作用
汚濁水の処理用として無機凝集剤が使用された
のはかなり以前からであるが、産業、工業の発展
に伴つて、急速な発展、変遷を経ており、1960年
代に英国、米国で塩基性塩化アルミニウムが発見
され、我国においてはその改良品が発明され(特
公昭47−21401号)広く使用されている。
その特長は加水分解およびイオンによる吸着、
フロツク架橋、凝集による汚濁分の分離にある。
本発明の発明者はこの無機凝集剤の他の物質を
加えて汚濁水の清澄化を図ることについて各種の
研究を重ねた結果、火成岩の一種で我国ではいた
るところに存在している〓紋岩等と、同様に我国
ではいたるところに存在している浮岩質堆積岩の
微粉に無機凝集剤を加えることによつて、汚濁物
質の沈澱が著しく急速に行なわれ、しかもその清
澄効果も格段にすぐれていることを発見するに至
つた。
本発明はその結果なされたものであり、汚濁水
に所定の粒度調整を行なつた〓紋岩等と、浮岩質
堆積岩の微粉と無機凝集剤とを所定の割合で加え
撹拌後生成した沈澱物を除去することによつて前
記目的を達成している。
以下各処理剤の成分について詳述する。
(a) 〓紋岩等微粉:前記したように〓紋岩等は火
成岩の一種であり、玻璃質に斜長石、アルカリ
長石等の長石を含み、さらに石英、雲母を含有
しており、岩漿が火山から吹き出して硬化した
ものである。我国ではいたるところに産出する
が、〓紋岩(rhyolite)は長野県更級郡稲山
町、神戸市兵庫区有馬町、長野市、等に産出す
るものが代表的なものである。また真珠岩
(perlite)は佐賀県伊万里市とか愛知県南設楽
郡鳳来寺山等に産出するものが著名である。さ
らに泥溶岩(mud−lava)の産地としては熊本
県天草、宮崎県臼杵郡高地穂町等が知られてい
る。これらの火成岩はいずれも30〜100μmの
ものを70%以上含有するように粒度調整される
が、30μm未満の微粉は汚濁分の凝集効果を妨
げ、沈降時間を著しく延長して清澄濁度を悪く
する欠点があり、また100μmを超えるものは
急速に沈降するため、吸着、凝集、フロツクの
生成を妨げる欠点を有する。
粒径30〜100μmのもの70%と定めたもう1
つの理由は、〓紋岩は、金、銀、銅等の金属鉱
床で、粉砕、微粉化、精錬の工程中において前
記範囲の粒径のものが不要品として副産するた
め、原価がきわめて廉いからである。
(b) 浮岩質堆積岩:浮岩質堆積岩はその主成分は
〓紋岩等と同様に玻璃質、長石、石英等から成
つている。異る点は〓紋岩等が火山より吹き出
した岩漿が硬化した火成岩であるのに対して、
浮岩質堆積岩は、岩石が破砕されて地表または
水域に沈澱堆積して生成した多孔性の岩石であ
る点である。
〓紋岩質浮岩堆積岩(rhyolitic pumice、
sedimentary rock)は通常軽石と呼ばれてい
るもので、地上に拡散堆積中に多種の成分(例
えば石灰質、炭酸質、珪酸質、ナトリウム、カ
リ、カルシウム類等)を吸着した火成岩が堆積
岩に変質したものである。また浮石質凝灰岩
(pumiceous tuff)は栃木県河内郡白山村に産
する大谷石として知られる岩石である。
これらの岩石はその粒径が30〜100μmにな
るように粒度調整がされている。30μm未満の
粒径のものは〓紋岩等の場合と同様、汚濁分の
凝集効果を妨げ、沈降時間を著しく延長して清
澄濁度を悪くする欠点があり、また100μmを
超える粒径のものは、急速に沈降するため吸
着、凝集、フロツクの生成を妨げる欠点を有す
る。また浮岩質堆積岩を加工して植物育成床や
みがき砂を製造する際に30〜100μm程度のも
のが規格外品として副産するため原価がきわめ
て廉いという点は〓紋岩等の場合と同様であ
る。
(c) 無機凝集剤:無機凝集剤は水の中に懸濁して
いるコロイド状の粒子の荷電を中和して粒子間
の引力が荷電による反発力を上回るようにして
水中の汚濁物質の凝集を促進する作用を持つも
のであり、安価で無害なものとしては、硫酸ア
ルミニウム(Al2(SO4)3・18H2O)、塩基性塩
化アルミニウム([Al(OH)oCl7-o]nのポリマ
ー)、硫酸第一鉄(FeSO4・7H2O)、塩化第二
鉄(FeCl3・6H6O)、硫酸第二鉄(Fe2
(SO4)3・nH2O)、塩素化コツパラス(Fe2
(SO4)3・FeCl3)等がある。上水道用に使用さ
れる無機凝集剤はJISK−1475でその規格が定
められている。
以上説明した処理剤(a)、(b)、(c)を適宜の割合で
配合し、汚濁水に加えて(汚濁水の性質如何によ
つては適切な高分子凝集剤および凝集助剤を加え
れば更によい結果が得られる。)、撹拌すれば、従
来法に較べてフロツクの生成速度、沈降性はきわ
めて大きくなる。
たとえば濁度14°乃至17°の汚れた河川水を処理
する場合、規定のシリンダーテスト法で撹拌した
後、処理水の全量を濁度2°まで低下させるに要す
る時間は従来法で約125分、本発明に係る方法で
は約9分であつた。このように、本発明に係る処
理法は従来法の1/5〜1/15の短時間で汚濁水
の高速処理化が可能である。
このような事実は、当業者にとつて全く予想も
できないことであり、従来何人もよくなし得なか
つたことである。
このような汚濁水の高速清澄化の作用機構は、
未だ明らかではないが、次のように推測すること
ができる。すなわち処理剤(a)(b)に含まれる斜長
石、玻璃質成分と多孔質の浮岩質堆積岩の成分構
造による吸着浄化作用に加えて粒度調整された粒
子のもつ負電荷が硫酸イオンを含む凝集剤の高正
電荷と適合した親和性を持ち、さらに処理剤(a)(b)
の微粉が凝集剤による巨大フロツクの生成及び架
橋を安定にし、適当な大きさに緊縮し、強固にす
る作用があるものと考えられる。また処理剤(a)、
(b)に含まれる成分および浮岩組織は水に溶解して
いる不純物を強力に吸着する作用があるものと推
測される。以上のような物理的、化学的作用によ
つて汚濁水の高速清澄化が達成されたものではな
いかと考えられる。
実際に本発明の処理法によつて得られた凝集沈
澱物を顕微鏡で調べると、処理剤(a)(b)の粒度を調
整した微粉は塩化アルミニウムの角錐単体間の汚
濁物凝集結合に凝着し、フロツクの大きさも2〜
3mmで架橋も密になつており、処理剤(a)(b)の効果
がよく観察される。これに対して従来法で行つた
場合、凝集のフロツクの大きさは約4〜7mmで塩
化アルミニウム角錐間のからみ合い、凝集および
フロツクの架橋も粗であることが観察される。
また本発明の処理法に係る顕微鏡調査ではフロ
ツクの生成に洩れた多数のアルミニウム微細結合
体(20〜100μm)も1μm前後以上の汚濁物を凝
集結合しており、これらにも洩れなく処理剤(a)、
(b)粒子が凝着していることが観察される。従来法
ではこれらの汚濁物を含む20〜1000μm程度のア
ルミニウム微細結合体は酸化した有機物の妨げ等
もあり、沈降も浮上もせず長時間水中に浮遊する
が、処理剤(a)(b)はそれらすべての微細結合体の浮
上を抑え、水から分離沈降させている実態がよく
観察される。
この処理剤(a)、(b)を添加して水を清澄化する処
理法は従来の処理法とは処理時間的には逆行する
ものである。すなわち、この処理剤(a)、(b)の添加
により強制沈降のみをさせれば普通は水質の低下
を生ずるのは当然である。しかしながら以上述べ
たような本発明に係る処理法では後述実施データ
の水質試験(第5表、第8表)に示すように処理
剤(a)、(b)が不純物の吸収、吸着に大きな寄与をし
ているものと推定されるのである。
粒度調整範囲外の処理剤(a)、(b)微粉(たとえば
4μm〜10μm)は質量電荷が僅少であるためか、
凝集剤との結合はなく、単体で水中を浮遊し、ま
た処理剤(a)(b)の粗大粒子(200μm以上)は塩化
アルミニウムの角錐に凝着して急沈している。こ
れらの観察から処理剤(a)、(b)の粒度調整した以外
の粒子は凝集剤の特性とする汚濁物の吸着、凝
集、架橋、フロツク沈降の機能を妨げていること
が判明する。
処理剤(a)、(b)は乾燥粒状で別々に使用し、また
は混合して使用する。処理剤cは液状で用いても
乾燥粉粒で用いても効果に影響はない。
また処理剤(a)、(b)、(c)は乾燥粉粒で使用するに
際しては、水分による溶融固化等がない限り、長
期間性能は安定している。
本発明に係る高速清澄処理法の対象となる水は
上水、産業排水、工業排水等であるが処理剤(a)、
(b)、(c)の添加量は、被処理水の性質すなわち濁
度、懸濁粒子の大きさ、PH、電荷性、成分の種類
等の他処理濁度、処理装置の機構、処理用添加剤
の有無その他で一概に云うことはできない。
しかしながら、一般的には微細粒子懸濁液に対
しては処理剤(a)は約10〜5000ppm、(b)は約10〜
500ppm、(c)は約10〜10000ppm程度であり、より
具体的に云えば、下水汚泥に準ずるような懸濁粒
子の濃度が大きい場合には処理剤(a)は約500ppm
〜5000ppm、(b)は10〜500ppm(c)は約500〜
10000ppmの範囲で使用する。また地下水、河川
水等比較的低濁度原液の場合には処理剤(a)は10〜
1000ppm、(b)は10〜100ppm(c)は10〜1000ppmの
範囲で使用する。
実際の処理に際しては被処理水の性質の必要事
項を調査した上で後記する実施例を参考にして実
験的に最も優れた処理剤(a)、(b)、(c)の配分を定め
ることが必要である。
本発明の特筆すべき利用法としては災害時の緊
急用水が考えられる。地震等の災害時に際して最
も不自由するのは水であるというのが定説である
が、災害時に風呂水、溜水等を本発明に係る方法
で処理した後、次亜鉛素酸ソーダを使用すること
によつて後述風呂残り湯の水質試験で実証される
ように簡単に飲用水が得られる。
(3‐5) 実施例
以下に本発明の効果等を具体的に理解するため
にホテル厨房排水、地下水、河川水および風呂排
水の高速清澄処理の実施例について説明するが、
これらはいずれも例示のためのものであり、本発
明がこの実施例のみに限定されることなく、他の
各種の水処理にも有効に実施できることは勿論で
ある、
実施例 1
(第1表、処理剤(a)は〓紋岩微粉、(b)は浮岩質
堆積岩微粉を使用)
産業排水の一例としてホテル厨房排水で1次篩
分沈降処理後の2次排水(濁度74°)を採集し、
これを1ジヤーテストで清澄度試験を行なつ
た。
本発明に係る処理法としては処理剤(a)600(b)
100ppmを混合し、処理剤(c)成分は水道用JIS規格
凝集剤700ppmと有機高分子1mgを添加する。被
処理液には処理後PH7.1となるようにNaOH溶液
を必要量加える。被処理液を撹拌しながら処理剤
(c)を注入し、次いで処理剤(a)(b)を添加し急速撹拌
(150rpm)を3分間行ない、続いて緩速撹拌
(40rpm)を10分間行なつた後10分間静置してか
らその上澄液の濁度とCODの水質を測定した。
その結果は第1表に示す通りである。
(3-1) Industrial application field The present invention relates to a treatment method for rapidly clarifying polluted water. ) containing fine powder of igneous rocks (hereinafter simply referred to as "silicon rocks, etc."), and floating rock sedimentary rocks containing plagioclase in the crystalline substance such as silicate floating rock sedimentary rocks and floating rock tuffs (hereinafter simply referred to as " When we say "floating sedimentary rock," we are referring to this.)
A high-speed clarification method for polluted water that makes the coagulation and sedimentation of pollutant components much more efficient than conventional methods by simultaneously injecting a pulverizing agent containing fine powder and an inorganic flocculant such as aluminum salt into polluted water. Regarding. (3-2) Prior art When treating water containing turbidity, clean water,
Purification treatment of industrial water, treatment of domestic wastewater such as hospitals, schools, hotels, kitchens, industrial wastewater, food, dyeing,
Treatment of industrial wastewater such as chemical and pharmaceutical industry wastewater can be considered, but in any case, sieving tanks, settling tanks,
Clarification is carried out by installing equipment such as a filtration tank and performing appropriate treatment operations such as adsorption, coagulation, and activation in the equipment. For example, in water purification treatment, chemical separation or sterilization of manganese and iron using chlorine, flocculants such as polyaluminum chloride, aluminum sulfate, and iron chloride, and coagulation aids such as slaked lime and soda ash are used to remove gravity. Treatment is carried out by appropriately combining physical and chemical treatment, sludge, biological treatment using active bacteria, etc. However, all of these conventional treatment methods for treating polluted water require large-scale treatment equipment, requiring large equipment costs and installation space, and have the drawbacks of requiring considerable time for treatment. . (3-3) Purpose of the invention The present invention improves the above-mentioned drawbacks of conventional treatment methods for clarifying polluted water, and makes it possible to clarify polluted water easily and in an extremely short time without requiring large-scale treatment equipment. The purpose of this project is to provide a treatment method for water treatment, as well as a simple method for securing emergency water in times of disaster. (3-4) Structure and operation of the invention Inorganic flocculants have been used for a long time to treat polluted water, but they have undergone rapid development and changes along with the development of industry. Basic aluminum chloride was discovered in the United Kingdom and the United States in the 1960s, and an improved version of it was invented in Japan (Japanese Patent Publication No. 21401/1989) and is widely used. Its features include hydrolysis and ion adsorption,
Separation of contaminants through flock cross-linking and aggregation. The inventor of the present invention has conducted various studies on adding substances other than this inorganic flocculant to clarify polluted water. Similarly, by adding an inorganic coagulant to the fine powder of floating rock sedimentary rocks, which are found everywhere in Japan, the sedimentation of pollutants is extremely rapid, and the clarification effect is also very good. I came to discover that The present invention was made as a result of this, and the precipitate formed after adding and stirring a predetermined ratio of grainstone, etc., which has undergone predetermined particle size adjustment, fine powder of floating sedimentary rock, and an inorganic flocculant to polluted water. The objective is achieved by removing the object. The components of each processing agent will be explained in detail below. (a) Fine powder such as sparite: As mentioned above, sparite is a type of igneous rock, and contains feldspars such as plagioclase and alkali feldspar in its vitreous substance, as well as quartz and mica. It is hardened by erupting from a volcano. Rhyolite is found everywhere in Japan, but the typical rhyolite is found in Inayama-cho, Sarashina-gun, Nagano Prefecture, Arima-cho, Hyogo-ku, Kobe City, and Nagano City. Also, perlite is famous for being produced in Imari City, Saga Prefecture, and Mount Horaiji, Minamishitara District, Aichi Prefecture. Additionally, Amakusa in Kumamoto Prefecture and Takachiho Town in Usuki District in Miyazaki Prefecture are known as producing areas of mud-lava. The particle size of all of these igneous rocks is adjusted to contain 70% or more of 30 to 100 μm particles, but fine powder less than 30 μm hinders the agglomeration effect of pollutants, significantly prolongs the settling time, and worsens the clarity and turbidity. In addition, those with a diameter exceeding 100 μm rapidly settle, which has the disadvantage of hindering adsorption, aggregation, and the formation of flocs. The other one is defined as 70% of particles with a particle size of 30 to 100 μm.
The reason for this is that crystallite is a deposit of metals such as gold, silver, and copper, and during the crushing, pulverization, and smelting processes, particles with particle sizes in the above range are produced as unnecessary products, so the cost is extremely low. It is the body. (b) Floating sedimentary rock: The main components of floating sedimentary rock are vitreous, feldspar, quartz, etc., similar to crystallite. The difference is that while rock is an igneous rock made from hardened rock ejected from a volcano,
Floating sedimentary rock is a porous rock that is produced by crushing rocks and depositing them on the surface of the earth or in water. 〓rhyolitic pumice,
Pumice (sedimentary rock) is usually called pumice, and is an igneous rock that adsorbs various components (e.g., calcareous, carbonate, silicic acid, sodium, potassium, calcium, etc.) during diffusion and deposition on the ground, and is transformed into a sedimentary rock. It is something. Pumiceous tuff is a rock known as Oya stone, which is produced in Hakusan Village, Kawachi District, Tochigi Prefecture. The grain size of these rocks is adjusted so that the grain size is 30 to 100 μm. Particles with a particle size of less than 30 μm have the disadvantage of hindering the agglomeration effect of pollutants, significantly prolonging the settling time, and worsening the clarity and turbidity, similar to the case of crystallite, etc., and particles with a particle size of more than 100 μm has the disadvantage that it sediments rapidly, which hinders adsorption, flocculation, and floc formation. In addition, when processing floating sedimentary rocks to produce plant beds and polishing sand, particles of about 30 to 100 μm in size are produced as substandard products, so the cost is extremely low, similar to the case with stonestone, etc. It is. (c) Inorganic flocculants: Inorganic flocculants neutralize the electric charge of colloidal particles suspended in water, so that the attractive force between the particles exceeds the repulsive force due to the electric charge, thereby coagulating the pollutants in the water. Cheap and harmless substances that have the effect of promoting n polymer), ferrous sulfate (FeSO 4 7H 2 O), ferric chloride (FeCl 3 6H 6 O), ferric sulfate (Fe 2
(SO 4 ) 3・nH 2 O), chlorinated Kotparas (Fe 2
(SO 4 ) 3・FeCl 3 ), etc. The standards for inorganic flocculants used for water supplies are determined by JISK-1475. The treatment agents (a), (b), and (c) explained above are blended in an appropriate ratio, and added to the polluted water (depending on the nature of the polluted water, an appropriate polymer flocculant and flocculation aid are added). (Additionally, even better results can be obtained.) If stirring is performed, the floc formation rate and sedimentation properties are significantly higher than in the conventional method. For example, when treating polluted river water with a turbidity of 14° to 17°, the conventional method takes approximately 125 minutes to reduce the total amount of treated water to a turbidity of 2° after stirring using the specified cylinder test method. , was approximately 9 minutes using the method according to the present invention. As described above, the treatment method according to the present invention enables high-speed treatment of polluted water in a short time that is 1/5 to 1/15 of the conventional method. Such a fact was completely unexpected for those skilled in the art, and was something that no one had been able to accomplish in the past. The mechanism of action for high-speed clarification of polluted water is as follows:
Although it is not clear yet, it can be inferred as follows. In other words, in addition to the adsorption purification effect due to the component structure of plagioclase and vitreous components and porous floating sedimentary rocks contained in treatment agents (a) and (b), the negative charge of the particles whose particle size has been adjusted contains sulfate ions. It has an affinity that is compatible with the high positive charge of the flocculant, and also has a
It is thought that the fine powder has the effect of stabilizing the formation and crosslinking of giant flocs by the flocculant, tightening them to an appropriate size, and making them stronger. Also, processing agent (a),
It is presumed that the components contained in (b) and the floating rock structure have the effect of strongly adsorbing impurities dissolved in water. It is thought that high-speed clarification of polluted water was achieved through the physical and chemical effects described above. When the coagulated precipitate actually obtained by the treatment method of the present invention was examined under a microscope, it was found that the fine powder with adjusted particle size of treatment agents (a) and (b) coagulated into the contaminant coagulation bonds between the pyramidal units of aluminum chloride. The size of the flock is 2~
At 3 mm, the crosslinking becomes denser, and the effects of treatment agents (a) and (b) can be clearly observed. On the other hand, when the conventional method is used, the size of the aggregated flocs is about 4 to 7 mm, and it is observed that the entanglement between the aluminum chloride pyramids, the agglomeration, and the crosslinking of the flocs are rough. In addition, microscopic investigations related to the treatment method of the present invention revealed that a large number of fine aluminum aggregates (20 to 100 μm) that were leaked during the formation of flocs also coagulated and bonded contaminants of around 1 μm or more. a),
(b) Particles are observed to be stuck together. In conventional methods, fine aluminum aggregates of about 20 to 1000 μm that contain these pollutants remain suspended in water for a long time without settling or floating due to interference from oxidized organic matter, etc. However, treatment agents (a) and (b) It is often observed that all these microscopic aggregates are suppressed from floating and allowed to separate and settle from the water. This treatment method in which water is clarified by adding treatment agents (a) and (b) is contrary to conventional treatment methods in terms of treatment time. That is, it is natural that if only forced sedimentation is caused by the addition of the treatment agents (a) and (b), the quality of the water will generally deteriorate. However, in the treatment method according to the present invention as described above, treatment agents (a) and (b) make a large contribution to the absorption and adsorption of impurities, as shown in the water quality tests (Tables 5 and 8) of the implementation data described below. It is presumed that they are doing so. Processing agents (a), (b) fine powder outside the particle size adjustment range (e.g.
4 μm to 10 μm) is probably because the mass charge is small.
There is no binding with the flocculant, and it floats alone in the water, and the coarse particles (200 μm or more) of treatment agents (a) and (b) adhere to the pyramids of aluminum chloride and quickly sink. From these observations, it is clear that particles other than those whose particle size has been adjusted in treatment agents (a) and (b) interfere with the functions of pollutant adsorption, flocculation, crosslinking, and floc sedimentation, which are the characteristics of flocculants. The processing agents (a) and (b) can be used separately in dry granular form or in combination. The effect of processing agent c is not affected whether it is used in liquid form or in dry powder form. Furthermore, when the processing agents (a), (b), and (c) are used in the form of dry powder, their performance is stable over a long period of time unless they are melted and solidified by moisture. The water targeted by the high-speed clarification treatment method according to the present invention is tap water, industrial wastewater, industrial wastewater, etc., and the treatment agent (a)
The amount of (b) and (c) added depends on the properties of the water to be treated, such as turbidity, size of suspended particles, pH, chargeability, type of components, etc., as well as treatment turbidity, mechanism of treatment equipment, and treatment It is not possible to make a general statement based on the presence or absence of additives and other factors. However, in general, for fine particle suspensions, the treatment agent (a) is about 10 to 5000 ppm, and the treatment agent (b) is about 10 to 5000 ppm.
500ppm, (c) is about 10 to 10,000ppm, and more specifically, when the concentration of suspended particles is large, similar to sewage sludge, the treatment agent (a) is about 500ppm.
~5000ppm, (b) is 10~500ppm (c) is approximately 500~
Use within the range of 10000ppm. In addition, in the case of relatively low turbidity stock solutions such as groundwater and river water, the treatment agent (a) should be
1000ppm, (b) is used in the range of 10 to 100ppm, and (c) is used in the range of 10 to 1000ppm. In actual treatment, after investigating the necessary properties of the water to be treated, the most excellent distribution of treatment agents (a), (b), and (c) should be determined experimentally with reference to the examples described later. is necessary. A notable use of the present invention is for emergency water use during disasters. It is a well-established theory that water is the most inconvenient thing in the event of a disaster such as an earthquake, but after treating bath water, standing water, etc. with the method of the present invention in the event of a disaster, sodium subzinc chlorate can be used. As a result, potable water can be easily obtained as demonstrated by the water quality test of leftover bath water described below. (3-5) Examples In order to specifically understand the effects of the present invention, examples of high-speed clarification of hotel kitchen wastewater, groundwater, river water, and bath wastewater will be described below.
These are all for illustrative purposes only, and it goes without saying that the present invention is not limited to these examples and can be effectively implemented in other various water treatments.Example 1 (Table 1) , the treatment agent (a) uses a fine rock powder, and the treatment agent (b) uses a fine powder of floating rock.) An example of industrial wastewater is the secondary wastewater from a hotel kitchen after the primary sieve sedimentation treatment (turbidity 74°) Collect the
This was subjected to a clarity test using a 1 jar test. The treatment method according to the present invention includes treatment agent (a) 600 (b)
100 ppm, and as the treatment agent (c) component, add 700 ppm of JIS standard flocculant for water supply and 1 mg of organic polymer. Add the necessary amount of NaOH solution to the liquid to be treated so that the pH becomes 7.1 after treatment. Add the processing agent while stirring the liquid to be processed.
Inject (c), then add treatment agents (a) and (b), perform rapid stirring (150 rpm) for 3 minutes, then perform slow stirring (40 rpm) for 10 minutes, and then let stand for 10 minutes. The turbidity and COD of the supernatant were measured.
The results are shown in Table 1.
【表】
表中本発明品とあるのは本発明に係る方法で処理
した処理水を示し(以下の各実施例も同様である
(ただし第2表以下の実施例では有機高分子は使
用していない。))、比較品とは比較品のために行
なつた方法(処理剤(a)、(b)を添加せず、その他は
本発明に係る処理法と同一の処理を行なつたも
の。)で処理した処理水(以下の各実施例でも同
様である。)を示している。
第1表の結果から明らかなように、本発明に係
る処理法では従来の処理法である比較品に較べて
濁度は急速に低下し優秀な成績を示しているが、
CODは殆ど変つていない。これは凝集剤の特性
を損つていないことを示している。
この例で示したように本発明に係る処理法にお
いては前記したようなジヤーテスト撹拌方法では
沈降清澄が速すぎるため、以下の実施例では撹拌
法として次に示すようなシリンダーテスト法を使
用することとする。
シリンダーテスト法:250ml用メスシリンダー
に試水250mlを採取し、処理剤(a)(b)を注入し、次
いで処理剤(c)を注入後、急速転倒30秒、緩速転倒
7分を行ない、静置する。清澄が急速に行なわれ
るため、液全量の濁度およびPHを測定する(液の
上部、中部、下部より等量採取して行なう。)。な
お上澄水については一部静置後の分刻みで記入す
る。処理剤(c)は上水道用凝集剤(JISK−1475規
格品)を使用する。
実施例2
(第2表、第3表、処理剤(a)(b)は実施例1と同
じ)
原水濁度98°、PH7.42の地下水を採取し、処理
剤(a)(b)を一定((a)500ppm、(b)100ppm)とし、処
理剤(c)の濃度を変化させることによる静置後30分
の濁度とPHの変化(第2表)および処理剤(a)(b)(c)
を定量にしたときの本発明品と従来法による比較
品の経時濁度変化(第3表)を測定した。[Table] In the table, the term "product of the present invention" indicates treated water treated by the method according to the present invention (the same applies to each of the following examples (however, in the examples from Table 2 onwards, no organic polymer was used). )), and the comparative product is a product that was treated using the same method as the method of the present invention (without adding treatment agents (a) and (b)). The same applies to each of the following Examples. As is clear from the results in Table 1, the treatment method according to the present invention shows excellent results with a rapid decrease in turbidity compared to the comparative product using the conventional treatment method.
COD hasn't changed much. This shows that the properties of the flocculant are not impaired. As shown in this example, in the treatment method according to the present invention, sedimentation and clarification are too fast with the jar test stirring method described above, so in the following examples, the cylinder test method shown below is used as the stirring method. shall be. Cylinder test method: Collect 250ml of sample water in a 250ml graduated cylinder, inject treatment agents (a) and (b), then inject treatment agent (c), then perform rapid inversion for 30 seconds and slow inversion for 7 minutes. , leave it still. Because clarification occurs rapidly, measure the turbidity and pH of the entire liquid (take equal amounts from the top, middle, and bottom of the liquid). For supernatant water, enter the information in minutes after it has been allowed to stand still. As the treatment agent (c), use a water supply flocculant (JISK-1475 standard product). Example 2 (Tables 2 and 3, treatment agents (a) and (b) are the same as in Example 1) Groundwater with a raw water turbidity of 98° and a pH of 7.42 was collected, and treatment agents (a) and (b) were used. Changes in turbidity and PH after 30 minutes of standing (Table 2) and treatment agent (a) by changing the concentration of treatment agent (c) with constant ((a) 500ppm, (b) 100ppm) (b)(c)
The changes in turbidity over time (Table 3) of the product of the present invention and a comparative product made by the conventional method were measured when quantified.
【表】【table】
【表】
この第2表の結果から、処理剤(c)の注入量が
200ppm以上であるとき、濁度の清澄化に著しい
効果があらわれていることがわかる。また第3表
の結果から、濁度の低下は比較品に較べて著しく
速く、また上澄液は静置後10分で0.8°という良好
な価を示し、比較品よりも優れていることがわか
る。
以上第1表ないし第3表から、濁度50°〜100°
前後の被処理液はその性質にもよるが処理剤(a)は
500〜1000ppm、処理剤(b)は約100ppm、処理剤(c)
は200〜1000ppm、が実用され、また濁度100°以
上の処理液については処理剤(a)(b)(c)の注入量はそ
れぞれ前記以上のものが必要となる。
実施例 3
(第4表、処理剤(a)(b)は実施例1と同じ)
神奈川県鶴見川下流の表流水(濁度14.5°、PH
7.5)を採取し、前記試験法で測定を行つた。こ
の場合処理剤(a)250ppm、(b)50ppm、(c)150ppm、
を原水に注入し、経時濁度、PHおよび静置後10分
の上澄水濁度、PHを発明品と比較品とで測定し、
その結果を第4表に示した。[Table] From the results in Table 2, the injection amount of treatment agent (c) is
It can be seen that when the concentration is 200 ppm or more, a remarkable effect appears in clarifying the turbidity. In addition, from the results in Table 3, the turbidity decrease is significantly faster than that of the comparative product, and the supernatant liquid shows a good value of 0.8° after 10 minutes of standing, indicating that it is superior to the comparative product. Recognize. From Tables 1 to 3 above, the turbidity is 50° to 100°.
It depends on the properties of the treated liquid before and after, but the treatment agent (a) is
500-1000ppm, processing agent (b) is approximately 100ppm, processing agent (c)
200 to 1000 ppm is practically used, and for processing liquids with a turbidity of 100° or more, the injection amounts of processing agents (a), (b), and (c) must be greater than the above. Example 3 (Table 4, treatment agents (a) and (b) are the same as Example 1) Surface water downstream of Tsurumi River, Kanagawa Prefecture (turbidity 14.5°, PH
7.5) was collected and measured using the test method described above. In this case, the treatment agent (a) 250ppm, (b) 50ppm, (c) 150ppm,
was injected into raw water, and the turbidity and pH over time and the supernatant water turbidity and pH after 10 minutes of standing were measured for the invented product and the comparative product.
The results are shown in Table 4.
【表】
表に示すように、静置後10分の濁度は比較品に
較べて格段に良好であり、また発明品においては
処理液全量についてもきわめて速い濁度の低下を
示している。
実施例 4
(第5表)
実施例3の原水を使用し、試験方法、処理剤、
水温等も実施例3と同一条件でテストを行ない、
第4表に示すような急速な濁度の低下が水質に及
ぼす影響を調べる目的で発明品と比較品との処理
液について水質の測定を行なつてみた。すなわ
ち、静置30分後液をNo.5A紙で過し、2種の
液と原水でCODその他の項目を測定した。そ
の結果は第5表に示す通りである。[Table] As shown in the table, the turbidity after 10 minutes of standing was much better than that of the comparative product, and the invention product also showed an extremely rapid decrease in turbidity for the total amount of treated solution. Example 4 (Table 5) Using the raw water of Example 3, the test method, treatment agent,
Tests were conducted under the same conditions as in Example 3, including water temperature, etc.
In order to investigate the effect of the rapid decrease in turbidity as shown in Table 4 on water quality, water quality was measured for treated solutions of the invention and comparative products. That is, after 30 minutes of standing, the liquid was filtered through No. 5A paper, and COD and other items were measured for the two types of liquids and raw water. The results are shown in Table 5.
【表】
表に示すように、濁度が急速に低下しているに
も拘わらず、本発明品は比較品に較べて水質が阻
害されることなく、各項目について向上がみられ
る。
実施例 5
(第6表、第7表、処理剤(a)は真珠岩微粉(b)は
実施例1と同じ)
家庭における残り湯(風呂水)(濁度13.5°、PH
7.24、濁質は主に水中に溶融または浮遊する有機
物)を1日経過後採取し試験を行なつた。この試
験は緊急用水として風呂水が使用できるか否かを
しらべるためのものである。本試験では本発明に
係る高速清澄処理が水質に及ぼす影響をみるため
にCOD等他の諸項目も併せて試験を行なつた。
まず第1試験では処理剤(c)を先に注入し、処理剤
(a)、(b)を後から注入する方法を採用した。処理剤
(c)は150ppmで固定し、処理剤(a)、(b)は1:0.2の
重量比で混合したものを用い、その混合物の注入
量を変えて濁度、PHを測定した。その結果は第6
表に示す通りである。[Table] As shown in the table, despite the rapid decrease in turbidity, the product of the present invention does not impede water quality compared to the comparative product, and improvements are seen in each item. Example 5 (Tables 6 and 7, treatment agent (a) and pearlite fine powder (b) are the same as in Example 1) Remaining hot water (bath water) at home (turbidity 13.5°, PH
7.24, Suspended matter (mainly organic matter dissolved or suspended in water) was collected after one day and tested. This test was conducted to determine whether bath water can be used as emergency water. In this test, various other items such as COD were also tested to see the effect of the high-speed clarification process according to the present invention on water quality.
First, in the first test, treatment agent (c) was injected first, and treatment agent (c) was injected first.
We adopted a method in which (a) and (b) were injected later. Processing agent
(c) was fixed at 150 ppm, processing agents (a) and (b) were mixed at a weight ratio of 1:0.2, and the turbidity and PH were measured by varying the injection amount of the mixture. The result is the 6th
As shown in the table.
【表】
また第2の試験では処理剤(a)、(b)は前記した
1:0.2の重量比で混合したもので300ppmとし、
処理剤(c)は150ppmとして、濁度、COD等の水質
を測定した。その結果は第7表に示す通りであ
る。[Table] In addition, in the second test, treatment agents (a) and (b) were mixed at a weight ratio of 1:0.2 as described above, and the concentration was 300 ppm.
The treatment agent (c) was set at 150 ppm, and water quality such as turbidity and COD was measured. The results are shown in Table 7.
【表】
尚このテストでは沈降物のみを排除して全液の
測定をした。
第6表から判るように、処理剤(a)、(b)の混合物
の注入量は、この条件下では300ppmで十分であ
り、それ以上の注入は特別な場合、例えば原水が
高い汚濁度を示した場合等を除き必要がないもの
と思われる。また第7表の結果から、本発明に係
る処理法が異常な高速清澄性を示しているにも拘
わらず水質はさらに優秀な数値を示し、凝集剤の
特性を全く損なわないことが併せて実証されてい
る。
実施例 6
(第8表、処理剤(a)(b)は実施例1と同じ)
実施例5の所見により、更に荷酷な条件下で家
庭風呂の残水に対して厚生省令水質基準に基き、
飲料水可否の試験を行つた。
家庭の風呂に2日間3人が連日入湯し、残り湯
を更に2日間放置した後、試水用原水とした。処
理剤(a)(b)は実施例1と同様であり、処理法は実施
例5と同様に行なつたが、処理剤は(a)+(b)=
200ppm、(a):(b)=1:0.1、(c)=100ppmとした。
また処理水には滅菌剤として次亜塩素酸ソーダを
残留塩素が1.0ppmになるように添加した。その
結果は第8表の通りである。[Table] In this test, only the sediment was excluded and the entire liquid was measured. As can be seen from Table 6, the injection amount of the mixture of treatment agents (a) and (b) is 300 ppm under these conditions, and injection of more than 300 ppm may be necessary in special cases, for example when the raw water has a high degree of pollution. It seems unnecessary except in cases where it is indicated. Furthermore, from the results in Table 7, it is also demonstrated that although the treatment method according to the present invention shows abnormal high-speed clarification, the water quality shows even better values and does not impair the properties of the flocculant at all. has been done. Example 6 (Table 8, treatment agents (a) and (b) are the same as Example 1) Based on the findings of Example 5, the remaining water in home baths met the Ministry of Health, Labor and Welfare ordinance water quality standards under even more severe conditions. Based on
A test was conducted to determine if the water was drinkable. Three people bathed in the bath at home for two consecutive days, and the remaining hot water was left for another two days and then used as raw water for testing. The treatment agents (a) and (b) were the same as in Example 1, and the treatment method was the same as in Example 5, but the treatment agents were (a)+(b)=
200ppm, (a):(b)=1:0.1, (c)=100ppm.
In addition, sodium hypochlorite was added to the treated water as a sterilizing agent so that the residual chlorine was 1.0 ppm. The results are shown in Table 8.
【表】
表の数値は厚生省令の水質基準に合格してお
り、しかも処理剤(a)、(b)、(c)の分量は少くて済ん
でいる。すなわちこの高速沈降処理法は緊急時に
大きな威力を発揮することは勿論であるが、その
他各方面での活用が可能でなる。なお、上記の清
澄水を活性微粉炭50%を含有する不織布の積層を
通過させることにより、CODを更に低下させる
ことができた。
以上の実施例が示すように本発明に係る水の処
理法によれば、汚濁水を速やかに清澄化すること
が可能であり、この実施例に示した以外の原水に
対しても処理剤(a)、(b)、(c)の濃度を適宜変更する
ことによつて前記実施例と同様にきわめて良好な
結果を得ることができる。
実施例に使用されている処理剤(a)はすべて粒径
30〜100μmのもの70%以上を含有するごとく粒
度調整をしたものであるが、この粒度調整の範囲
は概略の目安を定めたものであつて、この範囲を
多少逸脱したものでも本発明が有効に実施できる
のは当然である。処理剤(b)の粒径範囲の30〜
100μmも処理剤(a)の場合と同様概略の目安であ
つて、多少逸脱したものでも本発明は有効に実施
できる。
同様のことは各処理剤(a)、(b)、(c)の注入量につ
いても云うことができる。本発明においては成分
(a)の注入量は10〜5000ppm、(b)は10〜500ppm、
(c)は10〜10000ppmと限定しているがこれもまた
概略の目安を示したもので、原水の性情如何によ
つては、この範囲を多少逸脱したものでも本発明
が有効に実施できる。
(3‐6) 発明の効果
本発明は適宜粒度を調整した〓紋岩等、浮岩質
堆積岩および無機凝集剤の所定量を汚濁水に注入
して撹拌し生成した沈澱物を除去することによつ
て、汚濁水を高速に清澄処理することを可能とし
ており、次に示すようなすぐれた効果を有するも
のである。
(1) 従来使用されている各種凝集剤に較べて凝集
沈降時間は大巾に短縮される。前記した河川水
の例によれば、従来法の1/5〜1/15の短時
間で処理できる。
(2) 高速清澄処理が行なわれるにも拘わらず、従
来使用されている凝集剤の機能(有機物の除
去、濁度の低下)を損うことなく、濁度の低下
は極めて促進される。
(3) ケーキの含水率は低く剥離性も優れている。
本発明に係る方法によつて凝集沈降したケーキ
は含水率が50%前後と低く、剥離性も優れてい
るため、沈澱槽下部導管から容易に抜き取るこ
とができる。また抜き取られたケーキは自然乾
燥で容易に固化できるため処理が容易であると
いう特性を有している。
(4) 従来の方法に較べて処理剤(a)、(b)を必要とす
るが、この処理剤(a)、(b)は使用量もわずかでし
かも安価である。すなわち、処理剤(a)、(b)はそ
れぞれ〓紋岩等、浮岩質堆積岩の微粉から成つ
ているが、これらを原料としてみがき砂や植物
用の苗床を生産するに際し、また金、銀、銅の
製造に際しその製造工程の格外品または不要品
を篩で粒度を選別するだけで容易に使用できる
からである。処理剤(a)と(b)とは実施例において
も明らかなように1:0.1〜0.2の範囲で使用さ
れることが多いから、最初からその程度の割合
で混合したものを用いるのも便利である。
(5) 腐敗物等の有機物を容易に液中から分離沈降
せしめ、沈降状態を維持する。
(6) 水処理設備を新設するに際して、本発明に係
る方法によれば、撹拌、凝集、沈降、排出等の
設備費、敷地を大巾に節約することができる。
(7) 現在稼働中の水処理設備にも本発明に係る方
法は容易に利用でき、利用することによつてそ
の設備能力を増大することができる。
(8) 以上要するに水処理設備の向上しその設備費
を低減し、公害防除等に大きな貢献をもたら
し、また特に災害時における緊急用水の確保を
きわめて容易にする。[Table] The values in the table pass the water quality standards of the Ministry of Health and Welfare ordinance, and the amounts of treatment agents (a), (b), and (c) are small. In other words, this high-speed sedimentation treatment method is of course very effective in emergencies, but it can also be used in various other fields. Note that COD could be further reduced by passing the above clear water through a laminated layer of nonwoven fabric containing 50% activated pulverized carbon. As shown in the above examples, according to the water treatment method according to the present invention, it is possible to quickly clarify polluted water, and treatment agents ( By appropriately changing the concentrations of a), (b), and (c), very good results can be obtained as in the above embodiments. The processing agent (a) used in the examples all has a particle size of
The particle size has been adjusted so that it contains 70% or more of particles with a diameter of 30 to 100 μm, but this particle size adjustment range is a rough guideline, and the present invention is effective even if the particle size is slightly deviated from this range. Of course, it can be implemented. The particle size range of treatment agent (b) is 30~
100 μm is also a rough guideline as in the case of processing agent (a), and the present invention can be effectively practiced even if it deviates to some extent. The same can be said about the injection amounts of each treatment agent (a), (b), and (c). In the present invention, the ingredients
The injection amount for (a) is 10-5000ppm, (b) is 10-500ppm,
Although (c) is limited to 10 to 10,000 ppm, this is also a rough guideline, and depending on the characteristics of the raw water, the present invention can be effectively practiced even with a content slightly outside this range. (3-6) Effects of the Invention The present invention involves injecting a predetermined amount of floating rock, such as rockite, and an inorganic coagulant into polluted water and stirring the particles to remove the generated precipitate. Therefore, it is possible to clarify polluted water at high speed, and it has the following excellent effects. (1) Compared to the various flocculants used conventionally, the flocculation and sedimentation time is greatly shortened. According to the above-mentioned example of river water, it can be treated in a short time of 1/5 to 1/15 of the conventional method. (2) Despite the high-speed clarification process, the turbidity reduction is extremely accelerated without impairing the functions of the flocculants conventionally used (removal of organic matter, reduction of turbidity). (3) The moisture content of the cake is low and the peelability is excellent.
The cake coagulated and sedimented by the method of the present invention has a low moisture content of around 50% and has excellent peelability, so it can be easily extracted from the lower conduit of the settling tank. In addition, the extracted cake can be easily solidified by natural drying, so it has the property of being easy to process. (4) Although processing agents (a) and (b) are required compared to conventional methods, the processing agents (a) and (b) are used in small quantities and are inexpensive. In other words, treatment agents (a) and (b) are each made of fine powder of floating rock such as limestone, but when producing polishing sand and plant seedbeds using these as raw materials, they are also used to treat gold and silver. This is because when manufacturing copper, it is possible to easily use out-of-grade products or unnecessary products in the manufacturing process by simply sorting the particle size with a sieve. As is clear from the examples, processing agents (a) and (b) are often used in a ratio of 1:0.1 to 0.2, so it is also convenient to use a mixture at that ratio from the beginning. It is. (5) Easily separate and settle organic matter such as decayed matter from the liquid, and maintain the settled state. (6) When newly installing water treatment equipment, the method according to the present invention can significantly save equipment costs such as agitation, flocculation, sedimentation, and discharge, as well as site space. (7) The method according to the present invention can be easily applied to water treatment equipment currently in operation, and by using it, the equipment capacity can be increased. (8) In short, improving water treatment equipment will reduce equipment costs, make a major contribution to pollution control, and make it extremely easy to secure emergency water, especially in times of disaster.
Claims (1)
5000ppm、(b)の成分を有する処理剤を10〜
500ppm、(c)の成分を有する処理剤10〜10000ppm
を加え、撹拌した後生成された沈殿物を除去する
ことを特徴とする汚濁水の高速清澄処理法。 (a) 粒径30〜100μmのもの70%以上を含有する
ごとく粒度を調整した〓紋岩(rhyolite)、真
珠岩(perlite)、泥溶岩(mud−lava)等玻璃
質に長石(斜長石、アルカリ長石)を含む火成
岩微粉 (b) 粒径30〜100μmに粒度を調整した〓紋岩質
浮岩堆積岩(rhyolitic pumice、sedimentary
rock)、浮岩質凝灰岩(pumiceous tuff)等玻
璃質に斜長石を含む浮岩質堆積岩微粉 (c) 硫酸アルミニユウム、硫酸第一鉄、硫酸第二
鉄、塩化第二鉄、塩化アルミニユウム、ポリ塩
化アルミニユウム等の無機凝集剤[Scope of Claims] 1. Adding 10 to 10 times of a treatment agent having the following component (a) to polluted water.
5000ppm, 10 to 10% of treatment agent containing component (b)
500ppm, treatment agent containing component (c) 10-10000ppm
A method for high-speed clarification of polluted water, which is characterized by adding and stirring, and then removing the generated precipitate. (a) Feldspar (plagioclase, plagioclase, Igneous rock fine powder containing (alkaline feldspar) (b) Rhyolitic pumice, sedimentary rock with particle size adjusted to 30 to 100 μm
(c) Fine powder of floating sedimentary rocks containing plagioclase in the crystalline material, such as rock), pumiceous tuff, etc. (c) Aluminum sulfate, ferrous sulfate, ferric sulfate, ferric chloride, aluminum chloride, polychloride Inorganic flocculants such as aluminum
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6507884A JPS60209214A (en) | 1984-04-03 | 1984-04-03 | High-speed clarification process of filthy water |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6507884A JPS60209214A (en) | 1984-04-03 | 1984-04-03 | High-speed clarification process of filthy water |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60209214A JPS60209214A (en) | 1985-10-21 |
| JPH0533081B2 true JPH0533081B2 (en) | 1993-05-18 |
Family
ID=13276554
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6507884A Granted JPS60209214A (en) | 1984-04-03 | 1984-04-03 | High-speed clarification process of filthy water |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60209214A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4408302C2 (en) * | 1994-03-11 | 1996-04-04 | Zeochem Kft | Process for the manufacture and use of a solid composite product for water treatment |
| US6017310A (en) * | 1996-09-07 | 2000-01-25 | Andaris Limited | Use of hollow microcapsules |
| JP4655279B2 (en) * | 2006-02-15 | 2011-03-23 | 特定非営利活動法人まちなみ育成会 | Natural material water purification coagulating sedimentation agent |
-
1984
- 1984-04-03 JP JP6507884A patent/JPS60209214A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60209214A (en) | 1985-10-21 |
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