TW200827307A - The treating method of aquaculture waste-water and the apparatus thereof - Google Patents

The treating method of aquaculture waste-water and the apparatus thereof Download PDF

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TW200827307A
TW200827307A TW95147835A TW95147835A TW200827307A TW 200827307 A TW200827307 A TW 200827307A TW 95147835 A TW95147835 A TW 95147835A TW 95147835 A TW95147835 A TW 95147835A TW 200827307 A TW200827307 A TW 200827307A
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tank
algae
culture
wastewater treatment
wastewater
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TW95147835A
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Chinese (zh)
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TWI333482B (en
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Chung-Chyi Yu
Jun-Ming Chen
Wen-Long Lin
xian-ming Xu
jun-hong Liu
Yuan-Hui Wen
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Univ Nat Chunghsing
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    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W10/00Technologies for wastewater treatment
    • Y02W10/10Biological treatment of water, waste water, or sewage

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  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)

Abstract

The present invention relates to the treating method of aquaculture waste-water, which includes: providing an aquaculture tank, an aeration-typed waste water-treating tank connecting to aquaculture tank, a pump connecting to aquaculture tank and aeration-typed waste water-treating tank, and a lighting fixture; placing the alga pre-treated by fixation into the aeration-typed waste water-treating tank; starting the pump to make culture media in aquaculture tank flow into the aeration-typed waste water-treating tank; then removing out the nitrides in the culture media; and finally flowing back to the aquaculture tank. This invention also provides the apparatus relating to aforementioned method.

Description

200827307 九、發明說明: 【發明所屬之技術領域】 本發明係關於一種處理養殖廢水之方法與上述方法所 使用之裝置。 【先前技術】 污水處理時,——般可分為物理、化學與生物處理法, 而目前國内循環水養殖大多採用生物處理法,其中生物遽 馨 床在應用上雖獲致不錯的效果’但其進行石肖化處理往往伴 隨著驗劑添加、遽材逆洗與确酸氮累積等相關問題須待解 決。 因此’目前尚有以藻類進行污水之處理,係由於藻類 能以氨氮、亞硝酸鹽氮和硝酸鹽氮等氮化合物做為其營養 源攝取吸收,亦能於行光合作用時提供水中之溶氧,進而 達到改善水質的功效(葉等,1996 )。 目前商業上直接應用藻類處理廢水僅有氧化塘和高率 ⑩藻’也等’其巾氧化塘的設計原S是維持池塘好氧狀態,利 用好氧菌將廢水中有機物質分解,而藻類的作用為去除B0D 和無機營養鹽(吳等,1 992);高率藻池則是為獲得大量的 藻類,並可去除B〇D和營養鹽(〇3仙1(1,1978)。雖然氧化 塘和高率藻池具有經濟有效的優點,但亦存在著易受環境 改變而不易維持單一優勢藻種和藻類自出流水分離等問題 (盧等,19^3);且上述之氧化塘與高率藻池於循環廢水處 理時’大多未使用固定化技術將藻類固定,而有關固定化 200827307 技術使用纟’目前仍主要以減式或連續未循環再使用之 相關基礎測試為主。 疋以,為克服上述之問題,目前係利用固定化之技術, 而使固疋之微生物易與放流水分離、微生物不易流失、外 來=〖生物質對微生物的傷害減少、不需定期逆洗、處理效 率提高與可依廢水性質而有不同的微生物選擇等優點,而 使固定化處理廢水之研究逐漸受到重視。 利用單細胞微藻做固定化進行各種廢水處理,如去除 氮和磷等營養鹽、去除硝酸鹽、去除尿素等亦有相當多之 相關研究發表(Chevalier and de la Notie,1985; Garbisu et al., 1991; Mak and Trevan, 1988; Tam and Wong, 2 0 0 0),然而關於應用固定化藻類於水產養殖方面相關文 獻則仍相當少,且大多僅針對“批次式,,養殖時魚體排泄 物之氨氮去除進行研究,而有關實際應用在循環水系統研 究則厥如。 【發明内容】 有鑑於實際應用在循環水系統研究之厥如,本發明係 利用固定化技術將藻類固定後,再搭配循環水系統之使 用,進一步達到處理養殖廢水之目的。 本發明係提供一種養殖廢水之處理方法,係包括: 提供一養殖槽、一與養造槽連通之曝氣式廢水處理 槽、一連接在該養殖槽與該曝氣式廢水處理槽之抽水馬達 與一設置在該曝氣式廢水處理槽週邊之照明裝置; 6 200827307 中 放入經過固定化處理之藻 及 類於該曝氣式廢水處理槽 開啟該抽水馬達,而使該捭袭 u養槽之^養液能夠流至 曝氣式廢水處理槽進行氮化合物本 ϋ物之去除後,再返回該培養 槽中。 較佳地,該藻類係為綠藻。 較佳地’該綠藻係為小球藻。 杈佳地,該小球藻濃度為ΙΟΟχΙΟ4至4〇〇〇χ1〇4 cells/ml。更佳地,該小球藻濃度為12〇〇xl〇4ceUs/ini。 較佳地,該照明裝置係連續照射在該曝器式廢水處理 槽0 杈佳地,該照明裝置係設在該曝器式廢水處理槽之兩 側0 較佳地’該照明裝置之光照強度為i,〇〇〇至 15, OOOlux。更佳地,該照明裝置之光照強度為7, 7〇〇lux。 較佳地’該藻珠槽之水力停留時間(Hydraulic Residence Time,HRT)設定為1至6小時。更佳地,該 蒸珠槽之水力停留時間(Hydraui ic Residence Time,HRT) 設定為2小時。 另一方面,本發明提供一種養殖廢水之處理裝置,係 包括: 一養殖槽,係提供生物之生長且具有一出水口與進水 v ; 一與養殖槽連通之曝氣式廢水處理槽,係提供複數之 200827307 藻珠放置’且形成有一進水口與一出水口而分別與該養殖 槽之出水口與進水口連接,且該曝氣式廢水處理槽内形成 兩相鄰之槽室,其中一提供藻珠放置之藻珠槽與一緩衝 槽,且令該進水口係設於該藻珠槽'槽壁上,該出水口係 位於該緩衝槽之槽壁,而使培養液可依序經過該藻珠槽後 至該緩衝槽; 一連接在該養殖槽與該曝氣式廢水處理槽之抽水馬 達’係將該養殖槽内之培養液抽出後進入至該曝氣式廢水 ⑩處理槽;及 一設置在該曝氣式廢水處理槽週邊之照明裝置,係照 射在該曝氣式廢水處理槽上。 較佳地’該曝氣式廢水處理槽之頂端開口處係再鋪設 一阻隔網,該阻隔網係防止雜物掉落該藻珠槽中,且亦防 止藻珠由該藻珠槽中流出。 較佳地,該藻珠槽上鋪設之阻隔網係為尼龍網。 _ 較佳地’該曝氣式廢水處理槽係放置在高於該養殖种 處,而使該曝氣式廢水處理槽内之水位高於該養殖槽,而 能使該緩衝槽内之培養液回流至該養殖槽中。 較佳地,該抽水馬達係為沉水馬達而放置在該養殖槽 中。 9 藉此,本發明係利用固定化藻類之技術與搭配養殖廢 水之循環設計,而能不斷地處理養殖廢水,以達到改盖水 質之目的,且進一步改善以往利用硝化濾床所會遭遇之問· 題。 。 8 200827307 【實施方式】 本發明所使用之名詞「固定化處理」係指利用化學或 是物理之方法限制細胞的移動或是封閉細胞於某一空間 内,並允許反覆的利用該細胞,且該細胞之生理活性未受 固定化之影響。其中固定化方式係包括··微膠囊法 (Containment)、擔體結合法(Attachment)、交聯法(^〇ss — linking)、聚集法(Aggregati〇n)與膠體包覆法 (Entrapment),於本發明中係利用膠體包覆法將細胞包覆 在褐藻膠財,但不應限制本發明之固定化處理為上述之 方式。 水力停留時間(Hydraulic 本發明所使用之名詞200827307 IX. DESCRIPTION OF THE INVENTION: TECHNICAL FIELD OF THE INVENTION The present invention relates to a method for treating aquaculture wastewater and a device for use in the above method. [Prior Art] When sewage treatment, it can be divided into physical, chemical and biological treatment methods. At present, most of the domestic circulating aquaculture adopts biological treatment method, in which the biological Xinxin bed has achieved good results in application. The stone-sharpening treatment is often accompanied by problems such as the addition of the test, the backwashing of the coffin and the accumulation of acid and nitrogen. Therefore, there is still the treatment of sewage by algae, because algae can absorb and absorb nitrogen compounds such as ammonia nitrogen, nitrite nitrogen and nitrate nitrogen as nutrient sources, and can also provide dissolved oxygen in water during photosynthesis. To achieve the effect of improving water quality (Ye et al., 1996). At present, the commercial application of algae treatment wastewater only has an oxidation pond and a high rate of 10 algae 'equation'. The design of the towel oxidation pond is to maintain the pond aerobic state, using aerobic bacteria to decompose organic matter in the wastewater, and algae The role is to remove B0D and inorganic nutrients (Wu et al., 1 992); the high rate algae pool is to obtain a large amount of algae, and can remove B〇D and nutrient salts (〇3仙1 (1,1978). Although oxidized Ponds and high-rate algae ponds have the advantage of being economically effective, but there are also problems that are susceptible to environmental changes and are not easy to maintain the separation of single dominant algae species and algae from the runoff water (Lu et al., 19^3); and the above-mentioned oxidation ponds and When high-altitude algae ponds are used in the treatment of circulating wastewater, most of them do not use immobilization technology to fix algae, and the related use of immobilized 200827307 technology is still mainly based on the related basic tests of subtractive or continuous non-recycling. In order to overcome the above problems, the immobilization technology is currently used, so that the microorganisms of the solid sputum are easily separated from the discharged water, the microorganisms are not easily lost, and the foreign matter 〖the biomass is less harmful to the microorganisms, and no regular backwash is required. The treatment efficiency is improved and the microbial selection can be different depending on the nature of the wastewater, and the research on the fixed treatment wastewater has been paid more and more attention. The single cell microalgae is used for immobilization to treat various wastewaters, such as removing nitrogen and phosphorus nutrients. There are also a number of related studies published to remove nitrates and remove urea (Chevalier and de la Notie, 1985; Garbisu et al., 1991; Mak and Trevan, 1988; Tam and Wong, 2000), however The literature on the application of immobilized algae to aquaculture is still relatively small, and most of them are only for “batch type, ammonia nitrogen removal of fish excreta during aquaculture, and the practical application in the study of circulating water systems is as follows. SUMMARY OF THE INVENTION In view of practical application in the research of circulating water system, the present invention further utilizes the immobilization technology to fix the algae and then cooperate with the use of the circulating water system to further achieve the purpose of treating the aquaculture wastewater. The present invention provides a The treatment method of the aquaculture wastewater includes: providing a culture tank and an aerated wastewater treatment connected with the culture tank a pumping motor connected to the aquaculture tank and the aeration-type wastewater treatment tank and a lighting device disposed around the aeration-type wastewater treatment tank; 6 200827307, the immobilized algae and the like are placed in the exposure The gas-type wastewater treatment tank opens the pumping motor, and the nutrient solution of the raid-culture tank can be flowed to the aeration-type wastewater treatment tank for removal of the nitrogen compound, and then returned to the culture tank. Preferably, the algae is a green algae. Preferably, the green algae is chlorella. Preferably, the chlorella concentration is ΙΟΟχΙΟ4 to 4〇〇〇χ1〇4 cells/ml. More preferably, the The chlorella concentration is 12〇〇xl〇4ceUs/ini. Preferably, the illuminating device is continuously irradiated in the irrigator type wastewater treatment tank. Preferably, the illuminating device is disposed on both sides of the irradiant type wastewater treatment tank. Preferably, the illuminating intensity of the illuminating device is For i, 〇〇〇 to 15, OOOlux. More preferably, the illumination device has an illumination intensity of 7,7 lux. Preferably, the hydraulic residence time (HRT) of the algae bead is set to 1 to 6 hours. More preferably, the Hydraui ic Residence Time (HRT) of the steam bead is set to 2 hours. In another aspect, the present invention provides a treatment device for aquaculture wastewater, comprising: a culture tank for providing biological growth and having a water outlet and water inlet v; an aerated wastewater treatment tank connected to the culture tank; Providing a plurality of 200827307 algae placements and forming a water inlet and a water outlet respectively connected to the water outlet of the culture tank and the water inlet, and two adjacent tank chambers are formed in the aeration wastewater treatment tank, one of which Providing an algae bead and a buffer tank for placing the algae, and the water inlet is disposed on the groove wall of the algae groove, the water outlet is located on the groove wall of the buffer tank, so that the culture liquid can pass through The algae bead is followed by the buffer tank; a pumping motor connected to the aquaculture tank and the aerated wastewater treatment tank is taken out of the culture tank in the culture tank and then enters the aeration wastewater 10 treatment tank; And an illumination device disposed around the aeration-type wastewater treatment tank is irradiated on the aeration-type wastewater treatment tank. Preferably, the opening of the top end of the aerated wastewater treatment tank is further provided with a barrier network which prevents debris from falling into the algae channel and also prevents the algae from flowing out of the algae. Preferably, the barrier network laid on the algae groove is a nylon mesh. _ Preferably, the aerated wastewater treatment tank is placed above the culture, so that the water level in the aeration wastewater treatment tank is higher than the culture tank, and the culture liquid in the buffer tank can be Return to the culture tank. Preferably, the pumping motor is placed in the culture tank as a submersible motor. 9 Thereby, the invention utilizes the technology of immobilized algae and the circulation design of the mixed culture wastewater, and can continuously treat the aquaculture wastewater to achieve the purpose of changing the water quality, and further improve the problems encountered in the previous use of the nitrification filter bed. · question. . 8 200827307 [Embodiment] The term "immobilization treatment" as used in the present invention refers to the use of chemical or physical means to restrict the movement of cells or to block cells in a certain space, and to allow repeated use of the cells, and The physiological activity of the cells is not affected by immobilization. Among them, the immobilization method includes a microcapsule method, an attachment method, a cross-linking method, an aggregation method (Aggregati〇n), and an encapsulation method. In the present invention, the cells are coated on the alginate by a colloidal coating method, but the immobilization treatment of the present invention should not be limited to the above. Hydraulic retention time (Hydraulic)

Residence Time,ΜΊ),总 4匕處!—〆 」係指廢水停留在曝氣式廢水處 理槽之時間’於本發明中係利用馬達抽取培養液之流量控 制培養液停留在曝氣式廢水處理槽的時間。 产m、: 一養殖槽、一與養殖槽連通之曝氣式廢水 :二在該養殖槽與該曝氣式廢水處理槽之抽水 馬達與一設置在該曝氣式廢水處理槽週邊之照明裝置;放 理之藻類於該曝氣式廢水處理槽中;及開 行氣化合物之去除後,再返回該培養槽中) 錢㈤”顯:亞固广球藻可有效去除循環水養殖系統中 鈇(ΝΗ4 )與亞硝酸根離 均去除效率分別約為6二(:乂’其於實際養殖試驗平 為_與48.29心與6/°,而平均去除速率則分別約 ay因此,本發明係實際應用在養 9 200827307 殖系統上,處理後之廢水將循環再使用,且固定化藻池中 加裝曝氣裝置,並覆蓋一尼龍阻隔網於其頂端,以避免固 定化藻珠溢出。 本發明其他的特徵及優點將可明顯見於下列較佳具體 事實及申請專利範圍。 實例 下列實施例用於示範說明本發明。這些實施例不以任 何方式意欲限制本發明之範圍,但用於指示如何實施本發 明的材料及方法。 實施例1 :藻珠培養與固定 1 · 1藻類來源: 小球藻(sp·),由水試所生物技術組蘇 惠美博士提供。 1 · 2藻類培養: 以Bri s to 1培養液進行培養,其成分如表一所示。 表一 Bristol 培養液配方(Stein,1973) 每940 ml之滅菌去離子水加入下列濃縮液1〇 miResidence Time, ΜΊ), total 4 miles! —〆 ” means the time at which the wastewater stays in the aeration wastewater treatment tank. In the present invention, the flow rate of the culture fluid is controlled by the motor to control the time during which the culture fluid stays in the aeration wastewater treatment tank. Production m,: a culture tank, an aerated wastewater connected to the culture tank: a pumping motor in the aquaculture tank and the aeration wastewater treatment tank and a lighting device disposed around the aeration wastewater treatment tank The algae is treated in the aerated wastewater treatment tank; and after the removal of the gas compound, it is returned to the culture tank.) (5)": The solid algae can effectively remove the circulatory aquaculture system. (ΝΗ4) and the removal efficiency of nitrite are about 6 2 (: 乂 ', which is _ and 48.29 hearts and 6 / ° in the actual aquaculture test, and the average removal rate is about ay, respectively, the present invention is actually The application is applied to the 9200827307 colonization system, and the treated wastewater will be recycled and reused, and an aeration device is installed in the immobilized algae pool, and a nylon barrier mesh is placed on the top end thereof to avoid the immobilized algae beads overflowing. The other features and advantages of the invention will be apparent from the following description of the preferred embodiments of the invention. Show how to implement the materials and methods of the present invention. Example 1: Algae cultivation and fixation 1 · 1 algae Source: Chlorella (sp·), provided by Dr. Su Huimei, Biotechnology Group of the Water Test Institute. 1 · 2 algae cultivation : Cultured in Bri s to 1 medium, the ingredients are shown in Table 1. Table 1 Bristol culture formula (Stein, 1973) 940 ml of sterile deionized water was added to the following concentrate 1 〇mi

NaN03 10 g/400 ml CaCl2 · 2H20 1 g/400 ml MgS04 · 7H20 3 g/400 ml k2hpo4 3 g/400 ml kh2po4 7 g/400 ml NaCl 1 g/400 ml 1 · 3固定化藻珠之製作: 配製4%(w/v)的褐藻膠(Na-alginate)液1公升,並 於高壓滅菌釜中在12rc下滅菌30分鐘,待其冷卻後將等 體積之小球藻液加入褐藻膠液,即小球藻液比褐藻膠液為 « «200827307 1 : 1,並以磁石攪拌器(Fargo MS-90)攪拌約10分鐘,使 其達均勻地混合。取含有小球藻的褐藻膠液倒入50 ml之 滴定管中,滴定入濃度5%氯化鈣(CaCl2)液體内,每毫升 之褐藻膠混合液可形成20顆褐藻膠珠,其每顆藻珠直徑 約為5 mm,形成之藻珠靜置12小時後再以蒸餾水加以沖 洗,以去除殘餘之氯化鈣液。再將2公升固定為40000顆 藻珠與分別滅菌過的1公升之1 〇倍濃度人工合成廢液、〇. 2 公升亞硝酸根離子(N02-)儲備溶液、2公升硝酸根離子(NO〆) 儲備溶液及6· 8公升去離子水一併加入15公升之壓克力 桶置於光照強度約4300 lux、溫度設定為25°C之恆溫恆濕 槽(KATO SE-23ECN)内進行培養,並以雙孔曝氣機(永享 3^800〇)打氣,其曝氣量為每孔3〇1/111111,待培養48小 時將人工廢液中銨(NH4+)、亞硝酸根離子(N〇2-)與硝酸根離 子(NOf)皆去除後,以獲致高濃度小球藻之藻珠。 實施例2 :批次氮化合物去除試驗 2·1水質分析項目及方法 溫度、溶氧量(DO)、PH值、銨(腿4 + )、亞硝酸根離子(n〇2_) =硝酸根離子(Ν〇Γ)濃度,其各項量測方法如表一所示。 =測所知之數據,將再進一步進行統計分析,以了解小球 藻珠在各因子之下’對其去除氮化合物的影響。 11 200827307 表一各項水質量測方法表 項目 量測儀器 廠牌 量測方法 溫度 溶氧量感測器之 溫皮量測功能 WTW 直接量測 溶氧量 溶氧量感測器 WTW 直接量測 pH值 酸驗值量測儀 SUNTEXTX-2 直接量測 NH4+濃度 分光光度計 Spectronic 20 GENESYS 靛藍法 N〇2_濃度 分光光度計 Spectronic 20 GENESYS 分光光度計法 N〇3-濃度 分光光度計 Spectronic 20 GENESYS 馬錢子法 2 · 2銨(NH4+)去除試驗 2 · 2 · 1吸附試驗 將無藻之膠珠於人工合成廢液(成份如表二所示), 及無藻之膠珠與含有小球藻之藻珠於僅含銨(NH4+)的氨氮溶 液内,分別進行其膠珠之吸附與藻珠之除銨(NH4+)測試,探 討不同試液對膠珠之吸附影響,結果顯示無藻之膠珠於人 工合成廢液除銨(NH4+)試驗在測試達36小時,試液中的銨 (NH4+)全被無藻之膠珠吸附去除,當於第48小時添加氨氮 儲備溶液後,膠珠於第96小時後幾乎不再吸附銨(NH/), 其吸附之銨(NH/)飽和濃度約為38. 65 rag/1,而其達36小 時溶液之銨(Nil,)平均去除速率約為17. 93 mg/1 · day,無 藻之膠珠與含小球藻之藻珠於僅含銨(NH4+)之氨氮溶液,其 試驗結果之銨(NH4+)濃度變化於試驗初始24小時内相似, 12 200827307 但叙(NH4 )去除較人工合成廢液組緩慢,其去除效率僅達 10%左右,而人工合成廢液組則約達6〇% ,亦顯示人工人 成廢液中之微量元素具有促進膠珠吸附銨(NH4 + )之作用。 表一人工合成廢液配方(Tam and Wong,2000)NaN03 10 g/400 ml CaCl2 · 2H20 1 g/400 ml MgS04 · 7H20 3 g/400 ml k2hpo4 3 g/400 ml kh2po4 7 g/400 ml NaCl 1 g/400 ml 1 · 3 Immobilized algae beads: Prepare 1% (w/v) 1 - liter of Na-alginate solution, and sterilize in an autoclave at 12 rc for 30 minutes. After cooling, add an equal volume of chlorella solution to the alginate solution. That is, the chlorella liquid is more ««200827307 1 : 1 than the brown algae liquid and stirred by a magnet stirrer (Fargo MS-90) for about 10 minutes to make it evenly mixed. Pour the algae solution containing chlorella into a 50 ml burette and titrate into a 5% calcium chloride (CaCl2) liquid. Each milliliter of alginate mixture can form 20 alginate beads, each of which has an algae. The bead diameter was about 5 mm, and the formed algae beads were allowed to stand for 12 hours and then rinsed with distilled water to remove residual calcium chloride solution. Then fix 2 liters to 40,000 algae beads and separately sterilized 1 liter of 1 〇 concentration synthetic waste liquid, 〇 2 liters of nitrite ion (N02-) stock solution, 2 liters of nitrate ions (NO 〆 The stock solution and 6.8 liters of deionized water are added to a 15 liter gram cylinder and cultured in a constant temperature and humidity chamber (KATO SE-23ECN) with a light intensity of about 4300 lux and a temperature of 25 °C. It is pumped with a two-hole aerator (forever 3^800〇). The aeration volume is 3〇1/111111 per well. For the 48 hours to be cultured, ammonium (NH4+) and nitrite ions (N) in the artificial waste liquid. 〇2-) and nitrate ions (NOf) are removed to obtain a high concentration of chlorella algae beads. Example 2: Batch nitrogen compound removal test 2.1 Water quality analysis items and methods Temperature, dissolved oxygen (DO), pH, ammonium (leg 4 + ), nitrite ion (n〇2_) = nitrate ion (Ν〇Γ) concentration, the various measurement methods are shown in Table 1. = Measured data will be further analyzed statistically to understand the effect of chlorella beads under various factors on their removal of nitrogen compounds. 11 200827307 Table 1 Water Quality Measurement Method Table Project Measurement Instrument Brand Measurement Method Temperature Dissolved Oxygen Sensor Temperature Skin Measurement Function WTW Direct Measurement Dissolved Oxygen Dissolved Oxygen Sensor WTW Direct Measurement pH Acid Tester SUNTEXTX-2 Direct Measurement NH4+ Concentration Spectrophotometer Spectronic 20 GENESYS Indigo Method N〇2_Concentration Spectrophotometer Spectronic 20 GENESYS Spectrophotometer N〇3-Concentration Spectrophotometer Spectronic 20 GENESYS Horse Money Sub-method 2 · 2 ammonium (NH4 + ) removal test 2 · 2 · 1 adsorption test will be algae-free beads in synthetic waste liquid (components shown in Table 2), and algae-free beads and chlorella The algae beads were tested in the ammonia-nitrogen solution containing only ammonium (NH4+), and the adsorption of the beads and the ammonium removal (NH4+) test of the algae beads were carried out to investigate the adsorption effects of different test solutions on the beads. The results showed that the algae-free beads were The artificially synthesized waste liquid ammonium removal (NH4+) test was tested for 36 hours. The ammonium (NH4+) in the test solution was completely removed by the algae-free beads. When the ammonia nitrogen stock solution was added at the 48th hour, the beads were in the 96th hour. Hardly after Further, the ammonium (NH/) is adsorbed, and the ammonium (NH/) saturated concentration is about 38. 65 rag/1, and the average removal rate of the ammonium (Nil) solution is about 17.93 mg/1. · day, algae-free beads and algae-containing algae beads in ammonium (NH4+)-containing ammonia nitrogen solution, the test results of ammonium (NH4+) concentration changes similar to the initial 24 hours of the test, 12 200827307 but NH4) removal is slower than the synthetic waste liquid group, and its removal efficiency is only about 10%, while the synthetic waste liquid group is about 6〇%. It also shows that the trace elements in the waste liquid of human workers can promote the adsorption of ammonium by the beads. The role of (NH4 + ). Table 1 Synthetic Waste Liquid Formula (Tam and Wong, 2000)

Bacto-peptone 58.9 ms/1 Glucose 225.0 mg/1 (NH4)2so4 141.3 〇 mg/1 k2hpo4 33.7 mg/1 MgS04 · 7H20 50.0 mg/1 MnS04 · H20 5.0 mg/1 FeS04 · 7H20 2.2 mg/1 KC1 7.0 mg/1 CaCl2 3.7 mg/1 NaHC03 277.7 mg/1 2 · 2 · 2光週期試驗 光週期試驗是以綠色藻培養液(成分如表三所示) (蘇,1 999 )培養之小球藻進行藻珠固定化後,分別以連 縯與12 /12小時間歇光照’兩組光照條件進行藻珠批次式 除銨(NH4+)之試驗,試驗週期為48小時,以分析比較光照 週期對藻珠中藻細胞生長,及人工合成廢液中藻珠去除銨 參 (NH/)、pH值與溶氧量(D0)之影響,結果顯示,當綠色藻 培養液所培養藻液初始藻細胞濃度約為 226^104 cel ls/ml,所配製之褐藻膠液中之小球藻濃度則約為 113xl04 cells/ml,即每顆藻珠所含小球藻約為5.65χ1〇4 cel Is,而連續與間歇光照組之人工合成廢液初始銨(NH4+) 濃度則分別為25· 66與26· 16 mg/1。可發現第24小時間 歇光照組之小球藻濃度略高於連續光照組,試驗48小時 後連續光照組,由於連續光合作用之影響,其小球藻增殖 13 200827307 濃度則略高於間歇光照組,兩濃度分別約為742χΐ〇4與 597XW cells/ml ’即每顆藻珠所含小球藻分別約為 與29.85xl〇4 ceUs細胞。此外,連續與間歇 光照組之銨(NH/)濃度皆於48小時内完全被去除,其平均 去除速率分別為12.83與13.08 mg/1/day,達第24、小時 兩組之銨(NH/)濃度分別減少2〇3〇與1611丨而'、 值可發現係為先下降再回升,直_現象可沾介生兮α 八現象可此亦為藻珠攝取 (ΝΗ/)之速率較行光合作用時需-夤 吟而一乳化石反者快,及曝氣機 產生二氧化碳之影響;關於溶氧量(D〇)方面,兩組試驗 溶氧量(DO)分佈亦皆在4·〇_4·4 /丨以 社罢 士 β 且結果顯示 連繽光照組初始有較低之溶氧量(D〇),但試驗到第仙 時後其值則較高,其原因可能是帛48 、時時連續光照測 試組之小球藻濃度較高,因此光合作用較旺盛,導致有較 多氧亂產生,然其影響亦不顯著,兩組試驗之溶氧量(D〇 分佈也主要受曝氣量之影響。 表二綠色藻培養液配方(蘇,1999) 2 · 2 · 3不同濃度試驗 本試驗是以綠色藻培養液培養之小球藻進行藻珠固定 化後,分別以A、B與C三組設定銨(〇4+)濃度約為π、= 與35 mg/1之人工合成廢液進行比較試驗。此次試驗係於 三組初始銨(NH,)含量完全去除後之測試達 ^Bacto-peptone 58.9 ms/1 Glucose 225.0 mg/1 (NH4)2so4 141.3 〇mg/1 k2hpo4 33.7 mg/1 MgS04 · 7H20 50.0 mg/1 MnS04 · H20 5.0 mg/1 FeS04 · 7H20 2.2 mg/1 KC1 7.0 mg /1 CaCl2 3.7 mg/1 NaHC03 277.7 mg/1 2 · 2 · 2 Photoperiod test Photoperiod test was carried out with chlorella cultured in green algae culture solution (components as shown in Table 3) (Su, 1 999) After the beads were immobilized, the algae bead batch type ammonium removal (NH4+) test was carried out by continuous operation and 12/12 hour intermittent illumination 'two sets of light conditions. The test period was 48 hours to analyze and compare the photoperiod to the algae beads. The growth of algae cells and the effect of algae beads on the removal of ammonium (NH/), pH and dissolved oxygen (D0) in the synthetic waste liquid showed that the initial algal cell concentration of the algae cultured in the green algae culture solution was about For 226^104 cel ls/ml, the concentration of chlorella in the prepared algae solution is about 113x104 cells/ml, that is, the chlorella contained in each algae is about 5.65χ1〇4 cel Is, and continuous The initial ammonium (NH4+) concentrations of the synthetic waste liquids in the intermittent illumination group were 25.66 and 26·16 mg/1, respectively. It can be found that the concentration of chlorella in the intermittent light group was slightly higher than that in the continuous illumination group at the 24th hour, and the continuous illumination group after 48 hours of experiment, the chlorella proliferation 13 200827307 was slightly higher than the intermittent illumination due to the effect of continuous photosynthesis. The concentration of the two groups was about 742χΐ〇4 and 597XW cells/ml respectively, that is, the chlorella contained in each algae was about 29.85xl〇4 ceUs cells, respectively. In addition, the ammonium (NH/) concentrations of the continuous and intermittent illumination groups were completely removed within 48 hours, and the average removal rates were 12.83 and 13.08 mg/1/day, respectively, reaching the 24th and hourly groups of ammonium (NH/ The concentration is reduced by 2〇3〇 and 1611丨, respectively, and the value can be found to decrease first and then rise again. The phenomenon of straight _ can be absorbed by 兮α 八 phenomenon, which is also the rate of algae ingestion (ΝΗ/). For photosynthesis, it is necessary to use 夤吟 夤吟 乳化 乳化 乳化 , , , , , , , , , , , 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化 乳化_4·4 / 丨 社 社 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 且 缤 缤 缤 缤 缤 缤 缤 缤 光照 光照 光照 光照 光照 光照 光照 光照 光照 光照 光照 光照The concentration of chlorella in the continuous illumination test group was higher, so the photosynthesis was more vigorous, resulting in more oxygen generation, but the effect was not significant. The dissolved oxygen content of the two groups (D〇 distribution was also mainly affected by Effect of aeration. Table 2 Green algae culture solution formula (Su, 1999) 2 · 2 · 3 different concentration test This test is green After the algae cultured in the algae culture solution was fixed by algae beads, the artificial synthesis waste liquid with ammonium (〇4+) concentration of about π, = and 35 mg/1 was set up in groups A, B and C respectively. The test was conducted after the three groups of initial ammonium (NH,) content were completely removed.

咬外小時,及JL 後之接續試驗階段於試液中銨(NH/)合吾、< 八 里近於完全去除 200827307 時,添加新的氨氮儲備溶液以淮 从運仃+連績除銨(關4+)試驗,After the biting hours, and the subsequent test phase after JL, the ammonium (NH/) in the test solution, < Bali is almost completely removed from 200827307, adding a new ammonia nitrogen reserve solution to remove the ammonium from the transport + continuous performance 4+) test,

藉以觀察在此三種銨(腿4+)濃声A 辰度下固疋化藻珠之除銨(nh4+) ί月形,其中A組在第96、120、m 〇Ίβ , ^卜 心144、216與264小時添加 新的氨氮儲備溶液,使其人工人 八工口成廢液中銨(ΝΗ4+)濃度分 別回復至約 12.96、13、00、13 川 1/f 0〇 ^ D 1<5· 29、14· 32 與 14· 12 mg/l ; β組在弟96與216小時亦禾户 *加新的氰氮儲備溶液,其濃度 則分別為21· 96與24· 63 mg/i •而Γ , μ ^ i,而C組則在第96與240 小時添加新的氨氮儲備溶液,盆 狀共/辰度分別為31· 54與32. 84 mg/Ι,同時三組測試亦皆在試 曰牧忒驗弟192小時更換為新的人 工5成廢液’其濃度分別U3.〇9、22 65 #3i86mg/i, =分析比較人卫合成廢液中微量元素變化對藻珠隸(νη^ 二Ρ值之5、Ό果顯不,當人工合成廢液初始錢(ΝΗ4+) ^分別為14.90、26.90與35.72 mg/1,而綠色藻培養 液所培養藻液初始藻細胞濃度約# 1Q2x1q4 ,所 配製之褐藻膠液中之小球藻濃度則約為51xi〇4ceiis/mi, 即每顆蒸珠所含小球蒸約為2 55xlQ4 ceUs,A组於⑽ 小時,B、G兩㈣於144小料分料最高生長濃度,其 值分別為 255〇χ104、298〇χΐ〇4 盥%9 iU 興 Zb2〇xl〇4 cells/ml ,並 於最高值後均有下降趨勢且呈耩宕嘈 主穩疋/辰度,其下降原因可能 為人工合成廢液中微量元素未 木卞補充導致除銨(NH4+)速率 隻缓,造成提供藻珠中小球藻生長增殖所需能量較不足。In order to observe the ammonium removal (nh4+) ί 月 shape of the solidified algae beads under the three kinds of ammonium (leg 4+), the group A is in the 96th, 120th, m 〇Ίβ, ^ Buxin 144, 216 and 264 hours to add a new ammonia nitrogen stock solution, so that the concentration of ammonium (ΝΗ4+) in the waste of the workers' workers is restored to about 12.96, 13, 00, 13 Sichuan 1 / f 0 〇 ^ D 1 < 5 · 29,14·32 and 14·12 mg/l; β group in the 96 and 216 hours of Heshi* addition of new cyanide reserve solution, the concentration was 21.96 and 24·63 mg/i • Γ , μ ^ i, while in group C, new ammonia nitrogen stock solution was added at 96 and 240 hours. The potted total/length was 31·54 and 32.84 mg/Ι, and all three tests were also tested.曰 曰 忒 忒 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 192 ^ 2 Ρ 之 5, Ό 显 , 当 当 当 当 当 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工 人工Prepared The concentration of chlorella in the brown algae solution is about 51xi〇4ceiis/mi, that is, the steam contained in each steamed bead is about 2 55xlQ4 ceUs, the A group is at (10) hours, the B and G two (four) are at 144 small materials. The highest growth concentration of the material was 255〇χ104, 298〇χΐ〇4 盥%9 iU Xing Zb2〇xl〇4 cells/ml, and it showed a downward trend after the highest value. / Chen, the reason for the decline may be that the trace element in the synthetic waste liquid is not supplemented with hibiscus, resulting in a slow rate of ammonium removal (NH4+), resulting in insufficient energy to provide growth and growth of Chlorella in the algae.

:外’當試驗達36小時A組的卿h4+)完全被去除,而B 。c兩組的銨_,)亦皆在第42小時時被完全去除,三组 於此初始除銨(NIV)階段,達其完全去除之平均 15 200827307 隨初始銨(NHV)濃度增大而有提高之現象,分別為9. 93、 15·37、20·41 mg/l/day,且皆有穩定除銨(NH4+)的效果, ‘ A組於武驗達144小時時,第三次添加氨氮儲備溶液後 之半連續循環除銨(NH,)階段,藻珠之除銨(NH4+)速率有趨 緩現象’此狀況亦顯現在g與C之兩測試組,其原因可能 為人工合成廢液中之促進藻珠吸附攝取之微量元素被消耗 不足所致,亦與前述之吸附試驗在無微量元素供應下,所 獲得藻珠除銨(νη4+)效果較緩慢之情形一致。 ⑩ 2 · 2 · 4亞硝酸根離子(ν〇2-)去除試驗 本試驗首先配製無添加(NH4)2S〇4的滅菌人工合成廢液 980 ml ’並加入亞硝酸鹽氮儲備溶液2〇 ,即為試驗所 需之合成廢液。試驗是以Brist〇1培養液培養之小球藻進 行藻珠固定化,試驗週期為48小時,結果顯示初始藻細 胞?辰度約為182xlO4 cel ls/ml,所配製之褐藻膠液中之小 球藻濃度則約為91x104 cells/ml時,藻珠中小球藻在試 參驗終止時生長濃度達約347><1〇4 cel is/mi,顯示藻珠中小 球藻亦能攝取亞硝酸根離子(Ν〇Γ)來增殖;同時觀察亞硝 酸根離子(NOf)之濃度變化情形發現初始亞硝酸根離子 (N〇2 )濃度約為17·8〇 mg/1,於試驗達24小時時有9⑽以 上被藻珠去除,其去除的亞硝酸根離子(n〇2_)濃度約為 16·13 mg/i,並於試驗48小時後完全去除,顯示小球蕩 珠亦有良好除亞硝酸根離子(N0厂)之能力;此外,試驗之pH 值變化範圍係介於8·27-8·9〇之間,且pH值於開始時先 下降,其原因可能是曝氣機打氣所產生的二氧化碳造成 16 200827307 的;而溶氧量(DO)變化範圍介於4卜4 3 mg/1之間。: Outside 'when the test reached 36 hours, group A's Qing h4+) was completely removed, and B. The ammonium _,) of the two groups were also completely removed at the 42nd hour, and the three groups were in this initial ammonium removal (NIV) stage, reaching the average of the total removal of 15 200827307 with the increase of the initial ammonium (NHV) concentration. The phenomena of improvement are 9.93, 15·37, 20·41 mg/l/day, and all have the effect of stable ammonium removal (NH4+), 'A group is added for 144 hours when the test is 144 hours. After the ammonia-nitrogen reserve solution, the semi-continuous cycle of ammonium removal (NH,) stage, the rate of ammonium removal (NH4+) of algae beads slowed down. This situation also appeared in the two test groups of g and C, which may be due to synthetic waste. The trace elements in the liquid which promote the adsorption and uptake of the algae beads are insufficiently consumed, and the adsorption test described above is consistent with the slow effect of the removal of ammonium (νη4+) by the algae beads without the supply of trace elements. 10 2 · 2 · 4 nitrite ion (ν〇2-) removal test This test first prepares 980 ml of sterile synthetic waste liquid without added (NH4)2S〇4 and adds nitrite nitrogen stock solution 2〇, This is the synthetic waste liquid required for the test. The test was carried out by immobilizing algae beads with chlorella cultured in Brist〇1 culture medium for a test period of 48 hours. The results showed that the initial algal cell length was about 182×10 4 cel ls/ml, which was small in the prepared algae solution. When the concentration of chlorella is about 91x104 cells/ml, the growth concentration of chlorella in the algae beads is about 347><1〇4 cel is/mi at the end of the test, indicating that chlorella can also take up nitrous acid in the algae beads. Root ion (Ν〇Γ) to proliferate; while observing the concentration change of nitrite ion (NOf), the initial nitrite ion (N〇2) concentration was found to be about 17.8〇mg/1, which was tested for 24 hours. When 9 (10) or more were removed by algae beads, the concentration of nitrite ions (n〇2_) removed was about 16·13 mg/i, and it was completely removed after 48 hours of the test, indicating that the ball was also well removed. The capacity of the nitrate ion (N0 plant); in addition, the pH range of the test is between 8.27-8·9〇, and the pH value drops first at the beginning, which may be due to the aerator aeration. The carbon dioxide produced is 16 200827307; the dissolved oxygen (DO) varies between 4 and 4 3 mg/1

2 · 2 . 5硝酸根離子(N〇3-)去除試驗 本試驗亦先配製無添加(關4) Ah的滅菌人工合成廢液 800 ml ’再加入硝酸鹽氮儲備溶液2〇〇 “,即為試驗所需 之合成廢液。試驗是以Bristol培養液培養之小球藻進行 藻珠固定化,試驗週㈣72小時,結果顯示,初始藻細 胞濃度約I 88xlG4 cells/ml ’所製之褐轉液中之小 球藻濃度則約A 44xl〇4 cells/ml。試驗之初始確酸根離 子(仙3-)濃度約為28.44韃/1。小球藤生長濃度於試驗第72 小時時藻細胞濃度達約850x1〇4 cells/ml,由此可知硝酸 根離子⑽3—)亦是提供小球藻良好的氮源;此外’觀察确酸 根離子(Ν0Π可知試驗於第48小時約92%被去除,並在第 72小時完全去除,而前48小時之平均去除速率約為 y/1 · day ;此外pH值於初期亦會先下降,其原因亦可能 是受曝氣機產生的二氧化碳所影響;溶氧量變化範圍介^ 4. 0-4. 3 mg/Ι之間,且不隨藻細胞濃度增加而有上升。、 實施例3 :循環水養殖系統 請參閱第一圖所示,本發明使用之循環水養殖系統 係包括-養㈣(1 〇)、-與養㈣連通曝氣式廢水 理槽(20)、一連接在該養殖槽(1〇)與該曝氣式 水處理槽(20)之抽水馬達(3〇)與一設置在該曝: 式廢水處理槽(20)週邊之照明裝置(4〇),其中j 養殖槽(1 G )係提供生物之生長且具有—出水〇與進1 口,該曝氣式廢水處理槽(2〇)係放置在高於該養殖^ 17 2008273072 · 2.5 flux removal (N〇3-) removal test This test also prepares 800 ml of sterile synthetic waste liquid without addition (Off 4) Ah and then adds nitrate nitrate reserve solution 2, ie In order to test the synthetic waste liquid required for the test, the test was carried out by immobilizing the algae beads with the chlorella cultured in the Bristol culture solution, and the test week (four) was 72 hours. The results showed that the initial algae cell concentration was about I 88xlG4 cells/ml 'the brown turn The concentration of chlorella in the liquid was about A 44xl 〇 4 cells/ml. The initial acid ion ion (xian 3-) concentration of the test was about 28.44 鞑 / 1. The growth concentration of the small vine was at the 72nd hour of the test. Up to about 850x1〇4 cells/ml, it is known that nitrate ion (10)3-) is also a good nitrogen source for providing chlorella; in addition, 'observing the acid ion (Ν0Π, the test was about 92% removed at the 48th hour, and Complete removal in the 72nd hour, and the average removal rate in the first 48 hours is about y / 1 · day; in addition, the pH value will decrease first in the initial stage, which may be caused by the carbon dioxide generated by the aerator; The range of the amount varies between 4. 0-4. 3 mg / Ι, and does not accompany the algae The cell concentration increases and rises. Example 3: Circulating aquaculture system Please refer to the first figure. The recirculating aquaculture system used in the present invention includes - (4) (1 〇), - and (4) connected aeration. a wastewater treatment tank (20), a pumping motor (3〇) connected to the aquaculture tank (1〇) and the aeration water treatment tank (20), and a periphery of the exposure type wastewater treatment tank (20) Illumination device (4〇), wherein the j culture tank (1 G) provides biological growth and has a water outlet and an inlet, and the aeration wastewater treatment tank (2〇) is placed higher than the culture ^ 17 200827307

(1 〇)處,且該曝氣式廢水處理槽(2 〇)亦形成有一 進水口與一出水口而分別與該養殖槽之出水口與進水口連 接’該曝氣式廢水處理槽(20)内再形成一提供藻珠放 置之藻珠槽(21)與一緩衝槽(22),且令該進水口 係設於該藻珠槽(2 1 )之槽壁上,it出水口係位於該緩 衝槽(22)之槽壁,豸藻珠槽(2 1)之頂端開口處係 再鋪设一阻隔網,該阻隔網係防止雜物掉落該藻珠槽(2 1)中’且亦防止藻珠由該藻珠槽(21)中流出,使用 時,係令該抽水馬達(3 0 )將該養殖槽(1 〇 )内之培 養液抽出後進入至該曝氣式廢水處理槽(2 〇 )之藻珠槽 (2 1 )中進行去除氮化合物,之後培養液會流至該緩衝 槽(2 2 )中,最後因為該曝氣式廢水處理槽(2 〇 )位 置高於該養殖槽(1 〇),使其產生水位差而使該緩衝槽 (2 2)内已除氮之培養液回流至該養殖槽(1〇)中, 而完成循環。以下係為本發明實施例之詳細說明,但不用 以限制本發明’該養殖槽(1 〇 )之長寬高分別為?80、56〇 與480 mm,及由厚度5 mm之透明壓克力容器,且該曝氣 式廢水處理槽(2 0 )之長寬高分別為300、200與200 mm, 且以南150 mm與寬200 mm之壓克力板分隔成藻珠槽(2 1)與緩衝槽(22),其中該藻珠槽(21)之長寬高 分別為200、200與150 mm,且該曝氣式廢水處理槽(2 〇)之槽底部較該養殖槽(1〇)底部高約為62 cm,並 在該藻珠槽兩側約3 0 mm處,分別放置1只2 0 W日光燈(東 亞FL 20D-EX/18),其光照強度經由數位式照度計(TECPLE 18 200827307 530)里測約為77GG lux’以作為藻珠中小球藻所需之光源。 ^該抽水馬達(3 〇 )較佳地係為沉水馬達(Ri〇 6〇〇) 而设置在該養殖槽内,將該養殖#(1Q)中的培養液抽 送至該藥珠槽⑴)處理後,利用水位差的作用再流回 養殖槽(1 0)使用’此外,由於該阻隔網係覆蓋在該藻 珠槽上’而能夠防止藻珠由該藻珠槽中㈣,較佳地該阻 隔網係為尼龍網。其中上述之養殖槽(1 〇)有效水體約 為100公升,而藻珠槽(2 1 )處理廢水的有效水體約為 6公升。試驗期間,養殖槽(丄〇 )與藻珠槽(2 ι )分 別以2與1台之雙孔曝氣機(永享SF8〇〇〇)進行打氣以 提供吳郭魚所需之氧氣與藻#中小玉求藻所冑之二氧化碳。 3 1曝氣式藻珠槽之氮化合物去除試驗 為提供曝氣式藻珠槽所需之藻珠,本試驗皆以Brist〇i 培養液所培養的1公升小球藻液與1公升滅菌過之4%(w/v) 褐藻膠液均勻混合後,倒入50 ral滴定管滴定入濃度5% 氣化鈣液體内形成褐藻膠珠;製作成形之藻珠先靜置12 小時後再以蒸餾水加以沖洗,以去除殘餘之氯化鈣液,再 將2公升固定為40000顆藻珠與分別滅菌過的j公升之1〇 倍濃度人工合成廢液、0.2公升亞硝酸根離子(N〇厂)儲備溶 液、2公升硝酸根離子(Ν〇Π儲備溶液及6· 8公升去離子水 一併加入15公升之壓克力桶置於光照強度約43〇〇 lux、 溫度設定為25°C之恆溫恆濕槽(KATG SE-23ECN)内進行培 養’並以雙孔曝氣機(永享SF-8000)打氣,其曝氣量為每 孔3· 0 Ι/min ’待培養48小時將人工廢液中銨(NH^)、亞 200827307 以獲致高 硝酸根離子(N〇2_)與硝酸根離子(N〇1 2-)皆去除後, 濃度小球藻之藻珠後放入藻珠槽(2丄)中 本發明之試驗係令該藻珠槽(2 i )之7 (Hydraulic Residence Time,hrt)設定為 1水力停留時間 較佳地…小時,並採連續光照與曝氣,至6小時’ 〇)亦以連續曝氣之相同操作條件下進行測試養殖槽(1 珠組作為對照組。實際養瘦時,皆以總重約為且以無藻 尾吳郭魚為試驗養殖生物,試驗期間於早上8〇 g之3 4 〇 1:〇°分兩次平均投饒,每天投編為4g,·本 :ΓΓΓ;Τ下午5:°°開始,除了模擬養 ❹養殖試驗時水體取樣與藻珠中小球藻濃度 ;、 同外,其餘有放養吳郭魚之實際養殖試驗,i水質比曰不 試之前48小時為每間隔6小時,取樣位置點係於=測 槽中分別位於靠近進水口與出水口處以及中央處,並z養殖 深約10 cm處取樣,且進行—#遂曰 、 w於水 且進仃二重複夏測,並將三處量測少 平均值進行分析,此外,另於該曝氣式廢水處理槽 進行取樣,其取樣位置係位於進水σ與出水σ處而0 ) 該蒸珠槽(21)與該緩衝槽(22),且該進水口之= 樣方式為在養殖廢水經沉水馬達抽送未進入藻珠槽(: 20 3 ) 1 · 2結果 2 實際養殖試驗之藻珠組測試前培養藻珠的人工廢液, 3 )前即取樣’而出水口取樣方式則於藻珠槽(2 !) ψ 4 培養液流至該緩衝槽(2 2 )處附近取樣》 5 其初始銨(ΜΗ/)、亞硝酸根離子(Ν〇2_)與硝酸根離子(Ν〇 200827307 濃度分別約為18.52、20.12與18.03 mg/i,且實際養殖 試驗時藻珠組之固定化小球藻濃度量測,於試驗初始、第 120 與 312 小時分別約為 262x1 〇4、133〇χ1 〇4 與 143〇xl〇4 cells/ml,結果顯示實際養殖時吳郭魚之排泄物與殘餌分 解,導致循環廢水有足夠之營養源供應,小球藻濃度呈現 上升之趨勢。(1 〇), and the aeration wastewater treatment tank (2 〇) also forms a water inlet and a water outlet respectively connected to the water outlet of the culture tank and the water inlet 'the aeration wastewater treatment tank (20 Further, an algae bead (21) and a buffer tank (22) for providing algae placement are formed, and the water inlet is provided on the groove wall of the algae bead (2 1 ), and the outlet of the algae is located a groove wall of the buffer tank (22), and a barrier net at the top opening of the algae bead groove (2 1), the barrier net prevents the debris from falling into the algae groove (21) The algae beads are also prevented from flowing out of the algae bead tank (21). In use, the pumping motor (30) is used to extract the culture liquid in the culture tank (1) and then enter the aeration wastewater treatment tank. The nitrogen compound is removed from the algae groove (2 1 ) of (2 〇), and then the culture solution flows into the buffer tank (2 2 ), and finally the position of the aerated wastewater treatment tank (2 〇) is higher than the The culture tank (1 〇) is caused to generate a water level difference, and the nitrogen-removed culture liquid in the buffer tank (22) is returned to the culture tank (1〇) to complete the cycle. The following is a detailed description of the embodiments of the present invention, but it is not necessary to limit the invention. The length, width and height of the culture tank (1 〇) are respectively? 80, 56 〇 and 480 mm, and a transparent acrylic container with a thickness of 5 mm, and the length, width and height of the aerated wastewater treatment tank (20) are 300, 200 and 200 mm, respectively, and 150 mm south Separating into an algae groove (2 1) and a buffer tank (22) with an acrylic plate having a width of 200 mm, wherein the length, width and height of the algae groove (21) are 200, 200 and 150 mm, respectively, and the aeration The bottom of the tank of the wastewater treatment tank (2 〇) is about 62 cm higher than the bottom of the tank (1 〇), and about 20 mm on both sides of the algae groove, one 20 W fluorescent lamp is placed respectively (East Asia FL 20D-EX/18), whose light intensity is approximately 77 GG lux' measured by a digital illuminometer (TECPLE 18 200827307 530) as a light source required for chlorella in the algae beads. ^ The pumping motor (3 〇) is preferably a submersible motor (Ri〇6〇〇) and is disposed in the culture tank, and the culture liquid in the culture #(1Q) is pumped to the medicine bead tank (1)) After the treatment, the effect of the water level difference is used to flow back to the culture tank (10). In addition, since the barrier network is covered on the algae groove, the algae beads can be prevented from being in the algae groove (4), preferably The barrier mesh is a nylon mesh. The above-mentioned breeding tank (1 〇) has an effective water body of about 100 liters, and the algae sump (2 1 ) treats wastewater with an effective water body of about 6 liters. During the test, the culture tank (丄〇) and the algae bead tank (2 ι) were pumped with 2 and 1 double-hole aerators (forever SF8〇〇〇) to provide the oxygen and algae required by the Wu Guoyu. #中小玉求藻的胄的焦碳. 3 1 Nitrogen compound removal test of aerated algae channel is to provide algae beads required for aeration algae tank. This test uses 1 liter of chlorella solution cultured in Brist〇i culture medium and 1 liter of sterilized After 4% (w/v) alginate solution was uniformly mixed, pour into a 50 ral burette and titrate into a concentration of 5% calcium carbonate liquid to form alginate beads; the formed algae beads were allowed to stand for 12 hours before being treated with distilled water. Rinse to remove residual calcium chloride solution, and then fix 2 liters to 40,000 algae beads and separately sterilized j liters of 1 〇 concentration synthetic waste liquid, 0.2 liters of nitrite ion (N 〇 factory) reserve Solution, 2 liters of nitrate ions (Ν〇Π stock solution and 6.8 liters of deionized water together with a 15 liter acrylic barrel placed at a constant temperature of about 43 lux and a constant temperature of 25 ° C The culture is carried out in a wet tank (KATG SE-23ECN) and is aerated with a two-hole aerator (Always SF-8000) with an aeration of 3·0 Ι/min per well. Medium ammonium (NH^), sub-200827307 to obtain high nitrate ions (N〇2_) and nitrate ions (N〇1 2-) Thereafter, the concentration of the chlorella of the chlorella is placed in the algae groove (2丄). The test system of the present invention sets the 7 (Hydraulic Residence Time, hrt) of the algae groove (2 i ) to 1 hydraulic retention time. Good time...hours, continuous light and aeration, to 6 hours ' 〇) also tested under the same operating conditions of continuous aeration tank (1 bead group as a control group. In actual weight, all weight About and with the algae-free Wu Guoyu as the experimental breeding organism, during the test period, 8 〇1: 〇° in the morning was divided into two averages, and the daily vote was 4g, · Ben: ΓΓΓ; Τ afternoon Starting at 5:°°, in addition to the simulated water culture sampling and the concentration of chlorella in the algae beads; and the others, the rest have the actual aquaculture experiment of stocking Wu Guoyu, i water quality is not 48 hours before each test. 6 hours, the sampling position is in the = measuring tank located near the inlet and outlet and the center, and the sampling depth is about 10 cm, and the -#遂曰, w is in the water and the second is repeated. Summer test, and the three measurements are less averaged for analysis, in addition, the aeration The wastewater treatment tank is sampled, and the sampling position is located at the influent σ and the effluent σ and 0) the steam bead tank (21) and the buffer tank (22), and the water inlet is in the form of The water motor pumping did not enter the algae channel (: 20 3 ) 1 · 2 Results 2 The artificial waste liquid of the algae beads before the test of the algae group in the actual culture test, 3) the sample before the sample, and the sampling method of the water outlet was in the algae Slot (2 !) ψ 4 The culture solution flows to the vicinity of the buffer tank (2 2 ). 5 The initial ammonium (ΜΗ/), nitrite ion (Ν〇2_) and nitrate ion (Ν〇200827307 concentration respectively About 18.52, 20.12 and 18.03 mg/i, and the concentration of immobilized chlorella in the algae group during the actual culture test was about 262x1 〇4, 133〇χ1 〇4 at the initial test, 120 and 312 hours respectively. With 143〇xl〇4 cells/ml, the results showed that the excrement and residual bait of Wu Guoyu were decomposed during the actual breeding, which resulted in sufficient supply of nutrient source for circulating wastewater, and the concentration of chlorella showed an upward trend.

藻珠組與對照組試驗初始階段培養液之銨(nH4+)濃度 變化,係受吳郭魚持續排放之排泄物與殘餌之分解作用, 並在藻珠中小球藻攝取消耗較小下,導致其濃度在試驗初 始先上升再下降之現象’且其亦受培養液中亞硝酸菌之分 解及小球藻之攝取,整體變化亦以養輯最高,藤珠槽進 水口次之’而以緩衝槽出水口最低(如第二圖所示);養 =驗ΪΓ進水口與緩衝槽出水口之銨⑽4+)濃度分別 於试驗第96、96與6M、時達高峰,其值分別為2 H 99 L1二Γ’且緩衝槽出水口亦於試驗後期趨於零值, =與“槽進水口亦保持甚低之值,分別介於。.15_ • Ή卜G·12 mg/1之間;請再參閱第三圖所示,對 升再下降人二 體亦與蒸珠組相似先上 升再下降,但在未有小球藻之攝取下, 現有最低銨(nh4+)濃度情形,且 銨:7 口未顯 驗篦卟丨吐、去2 - —者之鉍(NH4 )濃度皆於試 驗第96小時達最尚’分別約為4 24、3. 同時亦在未有小球藤之作用 .19吨/1, Γ白冋於邊珠組養殖槽、蘿琏 槽進水與緩衝槽出水口三者曲 藻珠 ^ Ab . 最辰度’獲致藻珠槽放置 有效抑制系統中錢,)之增高現象,且其於試驗後 21 200827307 期亦受系統中有亞硝酸菌存在之影響,亦趨於被完全分解 去除,因此可知低密度放養吳郭魚時,培養液中的亞硝酸 菌就具有將銨(NH/)分解之效果,而不會使其產生持續累積 上升之情形。 此外,藻珠組與無藻珠組之亞硝酸根離子濃度變 化係於試驗前30小時藻珠槽出水口之亞硝酸根離子(n〇2_) 濃度較藻珠槽進水口高,而在第36小時後則緩衝槽出水 口之W酸根離子(N(V)較進水口低,顯示藻珠除亞硝酸根 離子(N〇2—)之能力已較攝取銨(NH4+)代謝產生亞硝酸根離子 (Ν〇Γ)高,當培養液初始銨(NV)濃度較低時,藻珠除銨(NH^) 過程中產生亞頌酸根離子(N(V)的時間會縮短,#第四圖所 示,圖中亦顯示藻珠組養殖槽、藻珠槽進水口與缓衝槽出 水口之亞硝酸根離子(Ν〇Γ)濃度分別在第192、192與216 小時達j高,其值分別約為η·31、1148與i〇39mg/i, 亦呈現藻珠槽出水口有最低值,而試驗達第312小時三者 ❿之濃度則分別下降至約為4· 11、4· 〇4與3· 76 mg/卜其下 2原因主要亦是受到藻珠攝取與麟酸菌分解之共同作用; 口月再參閱第五圖所示,對照組試驗初始階段與藻珠組呈相 ^現象,㈣珠槽中未有小㈣之代謝料及有硝酸菌之 分解作^導致其出水口之亞硝酸根離子⑽2_)濃度較進水 ,且養殖槽、藻珠槽進水口與緩衝槽之出水口皆在試 第144小時時,達最高濃度分別約為14, 89、15· 01與 、亦顯不在未有藻珠攝取有效抑制亞硝酸根離 2 )生成下,其皆高於藻珠組之養殖槽、藻珠槽進水口 22 200827307 與緩衝槽出水π的最高漠度,同時t培養液之亞硝酸根離 子(N〇2—)達最高濃度後,亦因受培養液中有硝酸菌存在增殖 之作用’開始呈現下降且趫於被完全去除之趨勢,由此可 知低被度放養吳郭魚時’培養液中的硝酸菌亦如同亞硝酸 菌對銨(NH4+)之作用,具有能將亞硝酸根離子(no2-)分解, 而使其不會在系統中持續累積上升。The change of ammonium (nH4+) concentration in the initial stage of the algae group and the control group was caused by the decomposition of the excrement and residual bait continuously discharged by the Wu nationality fish, and the consumption of chlorella in the algae beads was small, resulting in Its concentration rises and then falls at the beginning of the experiment' and it is also affected by the decomposition of nitrite bacteria in the culture solution and the uptake of chlorella. The overall change is also the highest in the cultivation, and the buffer is the second in the inlet of the vine bead. The outlet of the tank is the lowest (as shown in the second figure); the concentration of ammonium (10)4+) in the inlet of the inlet and the outlet of the buffer tank is respectively at the peak of the 96th, 96th and 6th, and the peak value is 2 H. 99 L1 二Γ' and the buffer tank outlet also tends to zero value at the end of the test, and the value of the tank inlet is also very low, between .15_ • G Bu G·12 mg/1; Please refer to the third figure. The rise and fall of the human body also rises and then decreases similarly to the steamed bead group, but in the absence of chlorella uptake, the minimum ammonium (nh4+) concentration is present, and ammonium: 7 mouths were not tested for vomiting, and 2 - the sputum (NH4) concentration was reached at the 96th hour of the test. Shang's are about 4 24, 3. respectively. At the same time, there is no role of small ball vines. 19 tons / 1, Γ white 冋 in the side of the bead group culture tank, Luojio tank water inlet and buffer tank outlet three curved algae Beads ^ Ab. The highest degree of 'accumulation of the algae bead placement effectively suppresses the increase in money in the system," and it is also affected by the presence of nitrite bacteria in the system after the test 21 200827307, and tends to be completely decomposed. It is removed, so that when the low-density stocking of the squid, the nitrite bacteria in the culture solution have the effect of decomposing ammonium (NH/) without causing a cumulative increase. Further, the algae group has no The change of nitrite ion concentration in the algae beads group was higher than the nitrite ion inlet (n〇2_) at the water outlet of the algae bead tank 30 hours before the test, and the buffer tank was discharged after the 36th hour. The W-acid ion of the nozzle (N(V) is lower than the inlet, indicating that the ability of the algae to remove the nitrite ion (N〇2-) has been higher than that of the ammonium (NH4+) to produce the nitrite ion (Ν〇Γ). When the initial ammonium (NV) concentration of the culture solution is low, the algae produces amnesium during ammonium (NH^) removal. The time of the root ion (N(V) will be shortened. #第图图, the figure also shows the nitrite ion (Ν〇Γ) of the algae bead culture tank, the algae bead inlet and the buffer tank outlet. The concentrations reached j high at 192, 192 and 216 hours, respectively, and their values were about η·31, 1148 and i〇39 mg/i, respectively, and the lowest value of the algae channel outlet, and the test reached the 312 hours. The concentration of sputum decreased to about 4·11, 4· 〇4 and 3.76 mg/b, respectively. The reason is mainly due to the combination of algae ingestion and decomposition of cinnamic acid bacteria. As shown in the figure, the initial stage of the control group is in phase with the algae group. (4) There is no small (four) metabolites in the bead tank and the decomposition of nitric acid bacteria causes the concentration of nitrite ions (10)2_) in the outlet to be higher. The water, and the water inlet of the culture tank, the algae bead inlet and the buffer tank are all at the first 144 hours, the highest concentration is about 14, 89, 15·01, and there is no effective inhibition of algae ingestion. The nitrite is separated from the 2) formation, which is higher than the culture tank of the algae bead group, the algae tank inlet 22 200827307 and the buffer tank effluent The highest indifference, at the same time, the highest concentration of nitrite ion (N〇2—) in the t-culture medium, and also due to the proliferation of nitric acid bacteria in the culture solution, began to decline and tend to be completely removed. Therefore, it can be seen that the nitric acid bacteria in the culture medium when the low-degree stocking of the Wuguo fish is also like the action of nitrite bacteria on ammonium (NH4+), which can decompose the nitrite ion (no2-) without causing it to Continue to accumulate in the system.

再者,藻珠組與對照組之硝酸根離子(N〇3_)濃度變化則 :第:圖與第七圖所示,兩組試驗之養殖槽、藻珠槽進水 口與緩衝槽出水π皆顯現持續平緩上升之現象。第六圖顯 不於試驗f U4小時前,蒸珠槽出水口有較高之值,其原 =係由於x到藻珠中小球藻攝取銨與亞确酸根離子 成化)之代謝影響,及培養液中有硝酸时在所致,同時亦 :到小球。藻攝取硝’酸根離子(N(V)較銨(〇4+)與亞硝酸根離 (N0j)k,導致藻珠去除硝酸根離子(N〇3_)之效果較不佳 ^寺只累積增大’養殖槽、藻珠槽進水口與緩衝槽出水口 ^驗^ 312小時之濃度分別㈣14⑽、15肩與15 98 :ϋ顯示無藻珠組之硝酸根離子(N(v)濃度,試驗 =皆以緩衝槽出水口最高,遭珠槽進水口次之,而以養 禅槽最低’顯示養㈣與藻珠槽皆有錢菌存在,且養殖 滿珠槽進水π與緩衝槽出水口於試驗達第312小時時, ^酸根離子⑽3_)濃度皆累積上升達約1? 8卜η.”與 ^«ng/卜·皆較有藻珠組者高,亦獲致藻珠能有 ^根離子(no3-)濃度上升之作用。 進一步計算銨(NH,)與亞硝酸根離子(Ν〇2·)之去 23 200827307 除效率’獲得如表四所示 去除效率(%卜〔(藻珠槽:二下戶;不: 衛禅“、t g/day)=〔(藻珠槽進水口濃度)-(緣 二實二養農度)〕x(藻珠槽每曰處理水量) 树之释 時‘Furthermore, the changes of nitrate ion (N〇3_) concentration in the algae group and the control group are as follows: Fig. 7 and Fig. 7 show that both the culture tank, the algae tank inlet and the buffer tank π are both The phenomenon of continuous and gradual rise appears. The sixth figure shows that before the test f U4 hours, the steam outlet of the steam bead has a higher value, and the original = is due to the metabolic influence of the uptake of ammonium and the acidification of chlorella by the chlorella in the algae beads, and When there is nitric acid in the culture solution, it is also caused by: to the small ball. The algae ingested nitrate 'acid ion (N(V) is more alkaline (〇4+) and nitrite away (N0j)k, which leads to the effect of algae removal of nitrate ion (N〇3_). Large 'culture tank, algae tank inlet and buffer tank outlet ^ test 312 hours of concentration respectively (four) 14 (10), 15 shoulders and 15 98: ϋ shows no algae beads group of nitrate ions (N (v) concentration, test = The water outlet of the buffer tank is the highest, followed by the inlet of the bead tank, and the lowest in the raising tank, the display of the (four) and algae channels are rich in bacteria, and the water in the full bead tank is π and the buffer tank outlet is At the 312th hour of the test, the concentration of acid ion (10)3_) increased to about 1? 8 η." and ^«ng/b· are higher than those with algae beads, and the algae can also have root ions. (no3-) the effect of increasing the concentration. Further calculation of ammonium (NH,) and nitrite ions (Ν〇2·) to go 23 200827307 In addition to the efficiency 'obtained as shown in Table 4 removal efficiency (% Bu [( algae groove :二下户;不: 卫禅", tg/day) = [(the concentration of the algae groove inlet) - (edge two real two agro-degree)] x (algae per tank treatment water volume) Time'

48 72 6 6 65 12 表中顯㈣珠域(NH4+)之去除 :":::? * 去除效率=照組之12%;兩組之亞確酸根離子⑽,) 率分別僅二細之去除效率低,其平均去除效 代謝旦 1 '、8%’藻珠組由於受到除銨(NH4+)過程中之 之録(:^ 式择J 硝酸根離子(N02 )去除速率,則依上述公 又藻珠組與無藻珠組之銨(NH/)平均去除速率,分別 24 200827307 :為26.61與o’ mg/day,亦以藻珠組有較高之值而有 單位時間較大里之錄(呵+ )被去除;其亞確酸根離子(肋2_) 平均去除速率則分別約為48.29與22.89叫/—亦顯2示 有藻珠之作用可獲致較大之去除速率,即在單位時間下有 較多之亞硝酸根離子(Ν〇Γ)被去除。 藻珠組之養殖槽、藻珠槽進水口與緩衝槽出水口之ρΗ 值變化,量測結果分別介於7. 99-8. 47、8. 27一8 61盘 U6-8.55之間’其平均值則分別為8 32 8 η與845:、48 72 6 6 65 12 The removal of the (4) bead (NH4+) in the table: ":::? * Removal efficiency = 12% of the group; the ytterbium ion (10) of the two groups, the rate is only two The removal efficiency is low, and the average removal efficiency of the metabolic 1', 8%' algae group is due to the removal of ammonium (NH4+) process (: ^ select J nitrate ion (N02) removal rate, according to the above public The average removal rate of ammonium (NH/) in the algae group and the non-algae group was 24 200827307: 26.61 and o' mg/day, respectively, and the algae group had a higher value and there was a larger unit time. (H+) is removed; the average removal rate of the arsenate ion (rib 2_) is about 48.29 and 22.89, respectively, and it is also shown that the effect of algae beads can result in a larger removal rate, that is, in unit time. The nitrite ion (Ν〇Γ) is removed. The value of the Η value of the water inlet of the algae bead, the water inlet of the algae and the outlet of the buffer tank, the measurement results are respectively 7.99-8 47, 8.27-86 61 between U6-8.55 'the average value is 8 32 8 η and 845:,

^藤珠槽出水π ρΗ值皆低於進水口;而對照組養道槽、 滅珠槽進水口與緩衝槽出水口之邱值範圍分別介於[I 為"78 2: 8 55與8.18-8.55之間,而其平均值則分别 Γη::與8.42’且藻珠槽進水口與緩衝槽出水口 之pH值4乎-致,顯示無藻珠的蒸珠槽耗驗作用較弱. 9同=致兩組之水質ΡΗ值皆介於適宜養殖之用… y· υ辦圍内。 此外,蒸珠組養殖槽、藥珠槽進水口與緩衝槽出水口 之溶氧量(DO)分別介於4.4_5 〇、4 3 5 θ出火口 ^ ^ 4.3-5.0 mg/1 之間,三者之平均溶氧量⑽)則皆約$ 4 對照組養殖槽、藤珠槽進水口與 g左右, 其分佈分別介於⑴.4、4.8、5.=\?容氧編) 其平均溶氧量⑽則分別約為5 ι、5·3與 … 組試驗結果顯示受到曝氣之影響,兩者之溶氧量二皆: 穩定分佈之現象,且㈣組巾藻珠槽之溶氧 顯提高,可能為試驗時藻珠數 )、…、明 里仍不夠多,其光合作用仍 25 200827307 不足以影響藻珠槽之溶氧量⑽。 _ #者’藻珠組養殖槽、藻珠槽進水口與缓衝槽出水口 又變化’1測結果分別介於23.2-27. 7、24. 3-28 4 ^ 24·3;28·^^^ 25 ^2;>5 ’、J6.4 C ’對照組養殖槽、藻珠槽進水口與緩衝槽出水口 1度則 77 別介於 20.3-25.9、20. 5-26· 8 與 20. 6-27. 0°c 之間’其平均溫度則分別約冑22.9、23.5與23. 6°C ;兩 、、且忒驗亦皆顯示藻珠槽受光照影響而有較高之溫度;同時 試驗期間兩組亦皆受氣候變化之影響,造成無藻珠組溫度 較藻珠組者低’此亦導致其溶氧分佈有較高之趨勢。且測 試期間亦發現兩組試驗之系統中溶氧有隨溫度下降而升高 之情形。 綜合上述兩實際養殖試驗結果,獲致藻珠具有穩定除 華4+)與亞硝酸根離子⑽。之能力’且藻珠亦能抑制銨 (NV)與亞硝酸根離子(N(V)之生成,其最高濃度皆低於無 藻珠組,肖時此結果亦在兩組之銨_4+)與亞硝酸根離子 ⑽2)之去除效率與去除速率分析中獲致,且藻珠組亦具有 較大之單位時間平均去除量;但當培養液中有銨⑽4 + )與亞 硝酸根離子(ΝΟ〆)存在時,由於藻珠攝取營養鹽之特性,其 去除靖酸根離子(N〇3-)之效果則較不佳,兩組$以藤珠組具 有抑制作用,獲致其累積增高之硝酸根離子⑽濃度較 低;而放養密度不高時之兩試驗組,其水質之pH值變化 相近,皆無劇烈波動並皆保持在適合養殖用水之pH值範 圍内;溶氧量(D0)之變化兩組皆不大,並受曝氣機打氣: 26 200827307 溫度變動之景彡變 p ^ 々片k 9且獲致溫度較低時培養液顯現有較高之 /合氧h形,同時培養液溫度亦受氣候變化之影響,且藻珠 槽文到光照之作用,兩組試驗期間其溫度皆較養殖槽高。 楞據本發明可作之不同修正及變化對於熟悉該項技術 者而言均顯然不會偏離本發明的範圍與精神。雖然本發明 已=述特疋的較佳具體事實,必須瞭解的是本發明不應被 制於該等特定具體事實上。事實上,在實施本發 馨 …、气方面對於熟習該項技術者而言顯而易知之 不同修正亦被涵蓋於下列申請專利範圍之内。 【圖式簡單說明】 I 圖·係為本發明一較佳實施例之示意圖。 圖.係為藻珠組之銨(NH4+)濃度變化曲線圖。 咖圖·係為對照(無藻珠)組之銨(NH4+)濃度變化 曲線圖。 # 第四圖·係為藻珠組之亞硝酸根離子(N02-)濃度變化 曲線圖。 第《5^ 、 θ •係為對照(無藻珠)組之亞硝酸根離子(N02-) k度變化曲線圖0 PI · 少 ^圃·係為藻珠組之硝酸根離子(no3_)濃度變化曲 線圖。 第七圖·係為對照(無藻珠)組之硝酸根離子(N〇3-) 涎度變化曲線圖。 27 200827307^The π ρ Η value of the vines in the vine bead is lower than the inlet; while the Qi value of the water channel of the control group, the water inlet of the ball and the outlet of the buffer tank are respectively [I is "78 2: 8 55 and 8.18 Between -8.55, and the average value of Γη:: and 8.42' respectively, and the pH value of the water inlet of the algae bead tank and the water outlet of the buffer tank is 4, indicating that the steam-free bead without algae beads has a weaker effect. 9 with = the water quality depreciation of the two groups are all suitable for breeding purposes... y· υ 围 围. In addition, the dissolved oxygen content (DO) of the steaming bead culture tank, the medicine bead tank inlet and the buffer tank outlet is between 4.4_5 〇 and 4 3 5 θ outlets ^ ^ 4.3-5.0 mg/1, respectively. The average dissolved oxygen (10)) is about $ 4 in the control culture tank, the inlet of the vine bead and the g, and their distribution is between (1).4, 4.8, 5.=\?? The oxygen content (10) is about 5 ι, 5·3 and ... respectively. The test results show that they are affected by aeration, and the dissolved oxygen content of both is the same: the phenomenon of stable distribution, and (4) the dissolved oxygen of the group of algae beads Increase, may be the number of algae beads in the test), ..., Mingli is still not enough, its photosynthesis is still 25 200827307 is not enough to affect the dissolved oxygen content of algae beads (10). _ #者'Algae group culture tank, algae bead tank inlet and buffer tank outlet change again'1 test results are between 23.2-27. 7, 24. 3-28 4 ^ 24 · 3; 28 · ^ ^^ 25 ^2;>5 ', J6.4 C 'Control culture tank, algae tank inlet and buffer tank outlet 1 degree 77 other than 20.3-25.9, 20. 5-26· 8 20. 6-27. Between 0 °c 'the average temperature is about 22.9, 23.5 and 23. 6 ° C; two, and the test also shows that the algae groove is affected by light and has a higher temperature At the same time, both groups were also affected by climate change, resulting in the temperature of the algae-free group was lower than that of the algae group. This also led to a higher tendency of dissolved oxygen distribution. During the test period, it was also found that the dissolved oxygen in the systems of the two groups increased with decreasing temperature. Based on the results of the above two actual aquaculture experiments, the obtained algae beads have stable removal of 4+) and nitrite ions (10). The ability 'and algae beads can also inhibit the formation of ammonium (NV) and nitrite ions (N (V), the highest concentration is lower than the algae-free group, this result is also in the two groups of ammonium _4 + ) and nitrite ion (10) 2) removal efficiency and removal rate analysis, and the algae group also has a larger average removal per unit time; but when the culture medium contains ammonium (10) 4 + ) and nitrite ions (ΝΟ 〆) When present, due to the ingestion of nutrients by algae beads, the effect of removing phthalate ions (N〇3-) is less favorable. The two groups have an inhibitory effect on the vinegar group, resulting in a cumulative increase in nitrate. The concentration of ion (10) was lower; when the stocking density was not high, the pH values of the two test groups were similar, and there was no sharp fluctuation and they were kept within the pH range suitable for aquaculture water; the dissolved oxygen amount (D0) was changed twice. The group is not large, and is inflated by the aerator: 26 200827307 The change of temperature changes p ^ 々片 k 9 and the culture medium shows a higher / oxygenated h shape when the temperature is lower, and the temperature of the culture solution is also Affected by climate change, and the effect of algae beads on the light, two test periods The temperature is higher than the culture tank. It is apparent to those skilled in the art that various modifications and variations can be made without departing from the scope and spirit of the invention. Although the present invention has been described in terms of specific details, it should be understood that the invention should not be In fact, the different amendments that are obvious to those skilled in the art in the implementation of the present invention are also covered by the following patent applications. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic view of a preferred embodiment of the present invention. Fig. is a graph showing the change of ammonium (NH4+) concentration in the algae group. The graph is a graph of ammonium (NH4+) concentration change in the control (no algae) group. #四图· is a graph showing the change of nitrite ion (N02-) concentration in the algae group. The variation of nitrite ion (N02-) k degree of the group "5^, θ• is the control (no algae beads)Fig. 0 PI · Less ^圃· is the concentration of nitrate ion (no3_) in the algae group Change graph. Figure 7 is a graph showing the change of nitrate ion (N〇3-) in the control (no algae) group. 27 200827307

【主要元件符號說明】 (10)養殖槽 (20)曝氣式廢水處理槽 (2 1 )藻珠槽 (2 2 )缓衝槽 (3 0 )抽水馬達 (4 0 )照明裝置 28 200827307 參考資料 吳錦、劉洪岐、吳淑您譯,(都留信也著)。1992。環境微生物。pp.50_ 54,PP.64·65。科技圖書股份有限公司。台北。 泰國蝦養殖池循 2. 平、ί文,、翁韶蓮、邱秋霞、張文柄。1996。 裱水之研九。農委會漁業特刊58:87_10(^台北。 •盧偉銘、盧重興、李李眉、陳伯中。1993。固定化藍綠藻處理含氮廢 水之研究。第十八屆廢水處理技術研討會論文集。台中。[Explanation of main component symbols] (10) Culture tank (20) Aeration wastewater treatment tank (2 1 ) Algae bead tank (2 2 ) Buffer tank (3 0 ) Pumping motor (4 0 ) Lighting device 28 200827307 References Wu Jin, Liu Hongyu, Wu Shu, you translated, (all letters are also). 1992. Environmental microorganisms. Pp.50_ 54, PP.64·65. Science and Technology Books Corporation. Taipei. Thai shrimp farming pool follows 2. Ping, ί文, Weng Yilian, Qiu Qiuxia, Zhang Wenshu. 1996. Research on the water. COA Fisheries Special Issue 58:87_10 (^Taipei. • Lu Weiming, Lu Chongxing, Li Limei, Chen Bozhong. 1993. Study on the treatment of nitrogenous wastewater by immobilized blue-green algae. Proceedings of the 18th Wastewater Treatment Technology Symposium. Taichung.

4·蘇惠美。1999。_料生物之培養與利用。ρρ·22-64。臺灣省水產試驗所。 基隆。 5. Chevalier P. and J. de la Noiie. 1985. Efficiency of immobilized hyperconcentrated algae for ammonium and orthophosphate removal from wastewaters. Biotechnology letters 17(6):395-400. 6_ Garbisu,C·,J· M· Gil,M_ L Bazin,D. O. Hall and J· L. Serra. 1991· Removal of nitrate from water by foam-immobilized Phormidium laminomm in batch and contiimous-flow bioreactors. Journal of Applied Phycology 3:221-234. 7· Mak, A. L. and M. D. Trevan. 1988. Urea as a nitrogen source for calcium-alginate immobilized Chlorella. Enzyme Microb. Technol. 10:207-213. 8. Oswald, W. J. 1978. The engineering aspects of microalgae. In Handbook of microbiology, 2nd Edition, Volume Π, A. I. Laskin and H. A. Lecheoalier, Eds·,ρρ·521-523、pp_531、ρρ·539-541· CRC Press,the United States· 9. Stein, J.R. 1973. Handbook of Phycological Methods: Culture Methods and Growth Requirements, pp.7-24. Cambridge University Press. Cambridge. 10. Tam, N.F.Y. and Y.S. Wong. 2000. Effect of immobilized microalgal bead concentrations on wastewater nutrient removal. Environmental Pollution 107:145-151. 294. Su Huimei. 1999. _The cultivation and utilization of biological materials. Ρρ·22-64. Taiwan Provincial Fisheries Laboratory. Keelung. 5. Chevalier P. and J. de la Noiie. 1985. Efficiency of immobilized hyperconcentrated algae for ammonium and orthophosphate removal from wastewaters. Biotechnology letters 17(6): 395-400. 6_ Garbisu, C·, J. M. Gil, M_ L Bazin, DO Hall and J. L. Serra. 1991· Removal of nitrate from water by foam-immobilized Phormidium laminomm in batch and contiimous-flow bioreactors. Journal of Applied Phycology 3:221-234. 7· Mak, AL and MD Trevan. 1988. Urea as a nitrogen source for calcium-alginate immobilized Chlorella. Enzyme Microb. Technol. 10:207-213. 8. Oswald, WJ 1978. The engineering aspects of microalgae. In Handbook of microbiology, 2nd Edition, Volume Π, AI Laskin and HA Lecheoalier, Eds·, ρρ·521-523, pp_531, ρρ·539-541· CRC Press, the United States· 9. Stein, JR 1973. Handbook of Phycological Methods: Culture Methods and Growth Requirements, Pp.7-24. Cambridge University Press. Cambridge. 10. Tam, NFY and YS Wong. 2000. Effect of immobilized Microalgal bead concentrations on wastewater nutrient removal. Environmental Pollution 107:145-151. 29

Claims (1)

200827307 十、申請專利範圍: 1 · 一種養殖廢水之處理方法,係包括: 提供’養殖槽、-與養殖槽連通之曝氣式廢水處理 槽、一連接在該養殖槽與該曝氣式廢水處理槽之抽水馬達 與一設置在該曝氣式廢水處理槽週邊之照明穿置· 放入經過固定化處理之藻類於該曝氣式廢水處理槽 中;及 開啟該抽水馬達,而使該培養槽之培養液能夠流至該 • 曝氣式廢水處理槽進行氮化合物之去除後,再返回該培養 槽中。 2 .如申請專利範圍第!項所述之養殖廢水之處理方 法,該藻類係為綠藻。 3 ·如f請專利範㈣2項所述之養殖廢水之處理方 法,該綠藻係為小球藻。 4如申明專利範圍第3項所述之養殖廢水之處理方 法,該小球藻濃度為1〇〇><1〇4至4〇〇〇χ1〇4 ceUs/mi。 籲 5 .如f請專利範圍第4項所述之養殖廢水之處理方 法,該藻類濃度為1200xl04cells/ml。 6如申喷專利範圍第1項所述之養殖廢水之處理方 法,該照明|置係連續照射在該曝器式廢水處理槽。 7 ·如中請專利範圍第6項所述之養殖廢水之處理方 法該”、、月裝置係設在該曝器式廢水處理槽之兩側。 8 ·如申請專科範圍第7項所述之養殖廢水之處理方 法,該…、月裝置之光照強度為1,〇〇〇至1 5, 0001 ux。 30 200827307 9 ·如申請專利範圍第 法,咳昭明F 1 項所述之養殖廢水之處理方 法該…明裝置之光照強度為7,7〇〇1虹。 方法' H申:專利範圍第1項所述之養殖廢水之處理 方法’該藻珠槽之水力停留 定為 κ6Λ raullcResidence 理方i:二申請專利範圍第10項所述之養殖廢水之處 τ. ^珠槽之水力停留時間(Hydraulic Residence200827307 X. Patent application scope: 1 · A method for treating aquaculture wastewater, comprising: providing a culture tank, an aeration wastewater treatment tank connected to the culture tank, a connection between the culture tank and the aeration wastewater treatment a pumping motor of the tank and a lighting disposed around the aerated wastewater treatment tank, placing the immobilized algae in the aerated wastewater treatment tank; and opening the pumping motor to make the tank The culture solution can be discharged to the aeration wastewater treatment tank for removal of nitrogen compounds, and then returned to the culture tank. 2. If you apply for a patent scope! The method for treating aquaculture wastewater according to the item, wherein the algae is a green alga. 3 · For the treatment of aquaculture wastewater as described in item 2 (4) of the patent, the green algae is chlorella. 4 The method for treating aquaculture wastewater according to claim 3, wherein the chlorella concentration is 1〇〇><1〇4 to 4〇〇〇χ1〇4 ceUs/mi. 5. In the case of f treatment of aquaculture wastewater as described in item 4 of the patent scope, the algae concentration is 1200 x 104 cells/ml. 6 The method for treating aquaculture wastewater as described in claim 1 of the patent application scope, wherein the illumination is continuously irradiated in the aerator type wastewater treatment tank. 7 · The method for treating aquaculture wastewater as described in item 6 of the patent scope is provided. The month and month are installed on both sides of the aerator-type wastewater treatment tank. 8 · As stated in item 7 of the application scope The treatment method of aquaculture wastewater, the light intensity of the ..., month device is 1, 〇〇〇 to 15 5, 0001 ux. 30 200827307 9 · If the application of the patent scope method, the treatment of the aquaculture wastewater described in the item C1 The light intensity of the device is 7,7〇〇1 rainbow. Method 'H Shen: The treatment method of the aquaculture wastewater described in the first paragraph of the patent range' The hydraulic retention of the algae groove is determined as κ6Λ raullcResidence : The application of the aquaculture wastewater mentioned in item 10 of the patent scope τ. ^The hydraulic retention time of the bead tank (Hydraulic Residence Time ’ HRT)設定為2小時。Time ’ HRT) is set to 2 hours. 一養瘦槽 π ; 種養殖廢水之處理裝置,係包括: ,係提供生物之生長且具有一出水口與進水 。 與養殖槽相通之曝氣式廢水處理槽,係提供複數之 藻珠放置,且形成有一進水口與一出水口而分別與該養殖 槽之出水口與進水口連接,且該曝氣式廢水處理槽内形成 兩相鄰之槽室,其中一提供藻珠放置之藻珠槽與一緩衝 槽’且令該進水口係設於該藻珠槽之槽壁上,該出水口係 位於該緩衝槽之槽壁,而使培養液可依序經過該藻珠槽後 至該缓衝槽; 一連接在該養殖槽與該曝氣式廢水處理槽之抽水馬 達’係將該養殖槽内之培養液抽出後進入至該曝氣式廢水 處理槽;及 一設置在該曝氣式廢水處理槽週邊之照明裝置,係照 射在該曝氣式廢水處理槽上。 1 3 ·如申請專利範圍第1 2項所述之養殖廢水之處 31 200827307 理裝置,該曝氣式廢水處理槽之藻珠槽開口處再舖設一封 閉開口的阻隔網,該阻隔網係防止雜物掉落該藻珠槽中, 且亦防止藻珠由該藻珠槽中流出。 1 4 ·如申請專利範圍第i 3項所述之養殖廢水之處 理裝置,該藻珠槽上鋪設之阻隔網係為尼龍網。 1 5 ·如申請專利範圍第1 4項所述之養殖廢水之處 理裝置’該曝氣式廢水處理槽係放置在高於該養殖槽處, 而使該曝氣式廢水處理槽内之水位高於該養殖槽,而能使 _ 該缓衝槽内之培養液回流至該養殖槽中。 16·如申凊專利範圍第15項所述之養殖廢水之處 理裝置’該抽水馬達係為沉水馬達而放置在該養殖槽中。 Η—、圖式: 如次頁 32A slimming tank π; a treatment device for breeding aquaculture wastewater, comprising: a system for providing biological growth and having a water outlet and water inlet. The aeration-type wastewater treatment tank connected to the culture tank is provided with a plurality of algae beads, and is formed with a water inlet and a water outlet respectively connected to the water outlet of the culture tank and the water inlet, and the aerated wastewater treatment Two adjacent tank chambers are formed in the tank, one of which provides an algae bead and a buffer tank for the algae placement, and the water inlet is disposed on the tank wall of the algae bead, and the water outlet is located in the buffer tank a tank wall, wherein the culture liquid can pass through the algae bead tank sequentially to the buffer tank; a pumping motor connected to the aquaculture tank and the aerated wastewater treatment tank is a culture liquid in the culture tank After being extracted, the device enters the aeration wastewater treatment tank; and a lighting device disposed around the aeration wastewater treatment tank is irradiated on the aeration wastewater treatment tank. 1 3 · If the aquaculture wastewater mentioned in the scope of patent application No. 12 is used, the planting device, the opening of the algae channel of the aeration wastewater treatment tank is further provided with a closed open barrier network, the barrier network is prevented. The debris falls into the algae channel and also prevents the algae from flowing out of the algae channel. 1 4 · If the aquaculture wastewater treatment device described in item i 3 of the patent application is applied, the barrier network laid on the algae groove is a nylon mesh. 1 5 · The treatment device for aquaculture wastewater as described in claim 14 of the patent application 'the aeration wastewater treatment tank is placed above the culture tank, so that the water level in the aeration wastewater treatment tank is high In the culture tank, the culture liquid in the buffer tank can be returned to the culture tank. 16. The aquaculture wastewater treatment device of claim 15 wherein the pumping motor is a submersible motor and is placed in the culture tank. Η—, schema: as the next page 32
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