离子交换法选择性回收污泥厌氧消化液中的磷

为探讨高效选择性回收污泥厌氧消化液中磷的离子交换方法,采用静态实验和动态实验研究了4种阴离子交换树脂（D213、D202、D301和DSQ）的磷回收性能,筛选了适合富磷污泥厌氧消化液选择性磷回收的高交换容量树脂。实验结果表明,D213、D202、D301和DSQ 4种树脂对正磷浓度为70 mg/L的厌氧消化液进行动态处理时,其最大穿透体积分别为3、7、17和90 BV;DSQ树脂磷交换容量远高于其他3种树脂,达到6 860 mg P/L湿树脂,是目前报道的高磷交换容量树脂的3~4倍;DSQ树脂能有效地抵抗厌氧消化液中有机质和硫酸根等阴离子的干扰;用NaOH溶液再生DSQ树脂并回收磷,磷洗脱率超过96%,洗脱液是高浓度含磷液,可作为磷矿石的优质替代品。研究表明,DSQ树脂是一种高效选择性分离磷的树脂,适用于污泥厌氧消化液的磷回收。     

利用白云石回收污泥厌氧消化液中的磷

为经济有效地从污泥厌氧消化液中回收磷,构建了以白云石提供钙镁源的磷回收方法,探讨了磷回收的工艺条件与效果。通过盐酸酸化厌氧消化液以降低其碳酸盐含量,同时利用白云石溶于冷稀盐酸的特性使其钙镁缓慢释放到酸化的厌氧消化液中形成第一步磷回收体系,考察体系酸化pH、白云石与厌氧消化液的固液比以及反应pH对白云石的钙镁释放和磷回收效果的影响;第一步磷回收后的上清液为第二步厌氧消化液磷回收提供钙镁源,研究投加钙磷摩尔比对磷回收效果的影响。实验结果表明,当固液比为5.0时,在酸化pH为4.0～4.5且酸化溶出时间为10 h以及反应pH为9.0的条件下,第一步磷回收产物以磷酸钙盐沉淀为主,厌氧消化液磷回收率及回收产物含磷率（以P2O5计）分别达到99.43%和38.49%;第一步磷回收后的上清液按一定的钙磷摩尔比投加到酸化后的厌氧消化液中进行第二步磷回收,当投加钙磷摩尔比为0.20时,在反应pH为9.0的条件下,回收产物同时含有磷酸钙盐和磷酸铵镁,厌氧消化液中氮、磷回收率分别达到13.19%和90.90%,回收产物氮、磷含量（以P2O5计）分别为0.26%和39.58%;经XRD、XRF、ICP及SEM等分析表征,2步磷回收的产物以磷酸钙盐和磷酸铵镁为主要成分,杂质少。研究表明,利用白云石为钙镁源,通过分别构建不同的磷回收体系可以分步从污泥厌氧消化液中经济有效地回收磷,且磷回收率和回收产物含磷率高。     

污泥厌氧消化液中碳酸盐对回收磷的影响

为探讨污泥厌氧消化液中碳酸盐对以磷酸钙盐形式回收磷的影响,以粉煤灰浸出液为钙源,考察了消化液中的碳酸盐对磷回收过程和磷回收产物性质的影响。实验结果表明,在反应pH为10、反应钙磷摩尔比为1.67、反应时间为10 m in的条件下,消化液碳酸盐浓度为2 400 mg/L(以CaCO3计)时,磷的回收率为78.53%,回收产物中磷含量(以P2O5计)为28.93%;对消化液进行盐酸预酸化使pH达到4及以下时,磷回收率接近100%,回收产物中磷含量(以P2O5计)达到43.08%。消化液中碳酸盐的存在易形成碳酸钙沉淀,从而降低了磷回收率、回收产物中磷含量以及回收产品的纯度;预酸化能够有效地去除消化液中的碳酸盐并降低了其对磷回收的不利影响。     

富磷污泥厌氧消化磷释放与回收的研究进展

生物强化除磷(EBPR)工艺会产生大量的富磷污泥。富磷污泥中的聚磷菌(PAOs)在厌氧消化过程中吸收外界碳源并释放大量正磷,高浓度的磷会对厌氧消化系统中厌氧微生物的代谢产生影响,使得消化过程更加复杂。富磷污泥厌氧消化过程会产生磷、氮、有机物和金属离子等物质,其中磷的回收利用可以减少磷矿资源的开采,从而实现磷资源的可持续循环利用。因此,研究富磷污泥厌氧消化过程中磷的变化规律,既为厌氧消化系统的稳定运行提供理论依据,又为磷的资源化回收利用提供参考。对富磷污泥厌氧消化释磷的相关研究成果以及磷回收进行分析和总结,并提出了相应的研究方向。     

Anammox-HAP颗粒污泥型膨胀床反应器的氮磷同步去除能力及污泥特性

为实现集成、高效的氮磷处理,提高厌氧氨氧化工艺的运行稳定性及功能集成性,搭建了一种新型的anammox-HAP颗粒污泥型膨胀床反应器.设置了 3个不同温度条件下的反应器,通过控制进入反应器中的钙、磷元素,以及调控反应器pH,探究了膨胀床反应器对氮、磷的同步去除能力,并对污泥特性进行了分析.结果表明:anammox-HA...     

硝酸盐对富磷剩余污泥厌氧消化的影响试验

以某采用 A/O 生物除磷工艺水质净化厂排出的富磷剩余污泥为研究对象,利用棕色消化瓶设计了 4 组厌氧消化试验,通过向其中投加NaNO3,考察硝酸盐对污泥消化过程的影响.结果表明,硝酸盐的存在导致 VSS 平均变化速率比空白样快 28.09 mg/(L·d),并且对污泥消化过程中的产甲烷阶段有一定的抑制作用;当硝酸盐存在时,厌氧氨氧化作用的发生导致上清液中的 N-NH4 变化速率减慢,硝酸盐对污泥消化过程中磷的释放有明显的抑制作用,当硝酸盐浓度高于 60 mg/L时,抑制作用明显.     

污泥龄对LSP & PNR污泥减量新工艺运行效能的影响

通过研究分析污泥龄(SRT)对富磷污水除磷的LSP&PNR污泥减量新工艺运行效果的影响,结果发现,延长污泥龄有利于提高系统的厌氧释磷能力,但不影响其总的除磷率,同时磷的回收比例增大,当SRT=50 d时,磷回收率取得最大值70.4%;LSP&PNR系统污泥龄增加,还有利于污泥产率的降低.试验还发现,排富磷污水除磷的长污泥龄LSP&PNR系统的除磷效率与污泥产率之间不存在制约关系,即系统可以同时获得优异的污泥减量与生物除磷效果,当SRT=50 d时,每降解1 kg COD仅产生0.143 kg污泥,而除磷率达最高值92.8%;LSP&PNR系统中SRT、DO与SVI之间存在一定的相关性,在供氧充足(DO=0.8～1.5 mg/L)条件下,SRT增加,SVI越高,但对于SRT为50 d的LSP&PNR系统,稳定运行时没有污泥膨胀之虞.     

利用白云石石灰去除与回收污泥厌氧消化液中氮和磷

以白云石石灰为实验材料去除与回收污泥厌氧消化液中的氮磷,通过小试实验研究不同投药固液比S/L、初始pH值、反应温度、搅拌速度及反应时间对去除与回收氮磷效果的影响。实验结果表明,在最佳投药固液比S/L为300mg/L,最佳初始pH值范围为8.5~9.5,反应温度为25.0℃,搅拌速度为150 r/min,反应时间为24 h条件下,氨氮(NH+4-N)和磷(PO3-4-P)的去除率分别为37.26%和89.60%。利用X射线衍射仪(XRD)、扫描电镜(SEM)对沉淀产物进行了表征,通过分析可知沉淀产物中含有磷酸铵镁(MAP),可实现废水中氮磷经济有效的回收。     

污泥水解酸化过程中污染物的释出及其影响因素研究

为了回收利用污泥中的有机物、氮和磷，研究了将厌氧污泥接种到吸附了污染物质的剩余污泥中，对污泥水解酸化的促进以及污泥中微生物所摄取污染物质的释出规律；揭示了厌氧条件下发酵时间、污泥量、pH和热处理对污染物释出的影响。结果表明，接种24 h后污染物被大量释放出来；在发酵时间为24 h条件下，污染物释出量与污泥质量成正比；吸附了污染物的剩余污泥相对含量越高，释磷量越大；污泥厌氧发酵时，碱性条件下有机物和正磷酸盐的释出量大于酸性条件，加碱调高pH可有效促进氨氮的释出；对吸附了污染物的剩余污泥进行短时热处理可有效缩短其厌氧发酵时污染物的释出时间。结果表明，控制污泥厌氧水解发酵条件可以促进污染物的释出，有利于下一步的回收。     

厌氧-立体循环一体化氧化沟除磷脱氮工艺中影响厌氧释磷的因素研究

本研究考察了厌氧-立体循环一体化氧化沟工艺(AN-IODVC)中厌氧释磷效果及诸影响因素.研究结果表明,AN-IODVC除磷脱氮系统中好氧污泥的VSS/MLSS值比厌氧污泥小,好氧污泥含磷量与厌氧污泥含磷量的差值和TP去除率、厌氧磷释放率及厌氧ORP呈良好的线性相关关系.厌氧磷释放的最佳条件为:污水COD/TP＞55,维持厌氧区ORP低于-400mV.     

反硝化聚磷一体化设备中的聚磷菌

研究了新型生物脱氮除磷新工艺反硝化聚磷一体化设备中反硝化厌氧池活性污泥的兼性厌氧微生物组成，数量及其在该除磷系统中功能，结果表明，稳定运行期反硝化厌氧池内活性污泥混合液的兼性厌氧微生物总数大大多于启动期，稳定期和启动期分离的兼性厌氧微生物有假单胞菌属，副球菌属和肠杆菌科，通过对三种纯菌株进行吸放磷研究，三种菌都有不同程度的聚磷功能，说明反硝化菌也具有聚磷作用。     

黄磷尾气中总磷及磷化氢的测定

电炉法生产黄磷的过程中会产生大量的尾气,其主要成分是CO(85％～95％)．还有磷、硫、氟、砷、CO2、N2、H2等杂质。黄磷尾气中的磷主要以P4、PH3、P2O5等形式存在。一般尾气经过水洗后．P2O5大部分被水吸收,尾气中主要是P4、PH3。采用分光光度法分析总磷和气体检测管测定磷化氢,效果良好。     

Surface water phosphorus dynamics in rice fields receiving fertiliser and manure phosphorus

A long-term randomised block field experiment was established in 1997 to study the dynamics of total P and dissolved P in the surface waters of rice fields receiving two application rates of fertiliser P and one rate of combined fertiliser and manure P. Preliminary results from the first two crops show that concentrations of both total P and dissolved P in the surface waters increased significantly following P application, especially during the first 2 weeks after application. P concentrations subsequently declined sharply within about 10 days, then declined steadily and remained almost constant from about 1 month after application. The initial increase in P concentration of surface waters was higher with increasing rate of fertiliser P, and the P concentration at the highest fertiliser rate peaked within about 1 week of application. The elevated P concentrations following fertiliser P application declined more rapidly than those following the combined application of fertiliser and manure P. When fertiliser and manure P were applied together, about 7 days later the surface water P concentrations were significantly higher than when the same rate of P (or double) was applied as fertiliser only. Disturbance of the surface soil by hand harrowing further increased the P concentrations in surface waters, with a subsequent decline to a steady value after about 1 week. Application of P fertiliser to the high P status soil in this experiment gave no crop yield response and may have increased the risk of pollution of adjacent surface waters through drainage from heavy rainfall events during the rice growing season. Therefore, fertiliser P should not be applied to such soils. If, however, fertiliser or manure P is applied, the application should be made during the dry winter to reduce P losses. Manure should be applied with particular care because of the higher risk of P losses to surface water arising from the relatively long period of high P concentrations in surface waters and the potential for greater release of P to field surface waters from the soil. Hand harrowing should also be avoided during wet weather to protect water quality.     

Capturing the lost phosphorus

Minable phosphorus (P) reserves are being depleted and will need to be replaced by recovering P that currently is lost from the agricultural system, causing water-quality problems. The largest two flows of lost P are in agricultural runoff and erosion (∼46% of mined P globally) and animal wastes (∼40%). These flows are quite distinct. Runoff has a very high volumetric flow rate, but a low P concentration; animal wastes have low flow rates, but a high P concentration together with a high concentration of organic material. Recovering the lost P in animal wastes is technically and economically more tractable, and it is the focus for this review of promising P-capture technologies. P capture requires that organic P be transformed into inorganic P (phosphate). For high-strength animal wastes, P release can be accomplished in tandem with anaerobic treatment that converts the energy value in the organic matter to CH₄, H₂, or electricity. Once present as phosphate, the P can be captured in a reusable form by four approaches. Most well developed is precipitation as magnesium or calcium solids. Less developed, but promising are adsorption to iron-based adsorbents, ion exchange to phosphate-selective solids, and uptake by photosynthetic microorganisms or P-selective proteins.     

Investigating phosphorus limitation in a fixed bed filter with phosphorus and nitrogen profile measurements

In 2000, the European Union adopted the European Water Framework Directive (WFD) (European Commission, 2000). The WFD focuses on increasingly stringent nutrient standards including ultra low nitrogen (< 2.2 mg N-total/L) and phosphorus concentrations (< 0.15 mg total phosphorus/L) in receiving surface waters and in relevant point sources like wastewater treatment plant (WWTP) effluent. Expansion of WWTPs with advanced post-treatment processes, like effluent filtration, is widely proposed to meet possible future effluent discharge standards. When combining biological nitrate-nitrogen and chemical phosphorus removal in one filter, phosphorus limitation in the denitrifying process may occur. This study investigated where in the filter bed and under which conditions phosphorus limitation occurs. Profile measurements for nitrate, nitrite, and orthophosphorus (PO4-P) combined with chemical oxygen demand (COD) and 02 were conducted. Results showed that the required PO4-P/NOx-N ratio is approximately 0.006 mg/mg after phosphorous precipitation and flocculation. Profile measurements have proven to be an applicable and useful tool. It showed how nitrate and orthophosphorus are removed through the filter bed based on the PO4-P/NOx-N ratio. When orthophosphorus is removed more rapidly and efficiently compared to nitrate, the PO4-P/NOx-N ratio decreases. When PO4-P/NOx-N ratio thresholds are approximately 0.006 mg/mg for a certain period of time and water temperatures varied significantly, orthophosphorus limitation may occur. Changing the filter-bed configuration or decreasing the coagulant dosage can prevent limitation of the denitrifying process because of a phosphorous shortage.     

Towards global phosphorus security: a systems framework for phosphorus recovery and reuse options

Human intervention in the global phosphorus cycle has mobilised nearly half a billion tonnes of the element from phosphate rock into the hydrosphere over the past half century. The resultant water pollution concerns have been the main driver for sustainable phosphorus use (including phosphorus recovery). However the emerging global challenge of phosphorus scarcity with serious implications for future food security, means phosphorus will also need to be recovered for productive reuse as a fertilizer in food production to replace increasingly scarce and more expensive phosphate rock. Through an integrated and systems framework, this paper examines the full spectrum of sustainable phosphorus recovery and reuse options (from small-scale low-cost to large-scale high-tech), facilitates integrated decision-making and identifies future opportunities and challenges for achieving global phosphorus security. Case studies are provided rather than focusing on a specific technology or process. There is no single solution to achieving a phosphorus-secure future: in addition to increasing phosphorus use efficiency, phosphorus will need to be recovered and reused from all current waste streams throughout the food production and consumption system (from human and animal excreta to food and crop wastes). There is a need for new sustainable policies, partnerships and strategic frameworks to develop renewable phosphorus fertilizer systems for farmers. Further research is also required to determine the most sustainable means in a given context for recovering phosphorus from waste streams and converting the final products into effective fertilizers, accounting for life cycle costs, resource and energy consumption, availability, farmer accessibility and pollution.     

沉积物中磷形态及影响其释放的环境因素研究进展

磷是控制水体富营养化最关键的营养物质,在外源磷得到控制之后,内源磷通过各种复杂过程再次进入水体,成为水体富营养化的主要磷污染源。目前,国内外对底泥磷的相关研究已非常多,但缺乏系统的整理和总结。从底泥磷的形态和影响其释放的环境因素2个方面进行了系统总结,介绍了底泥磷的主要形态、释放机制,分析了环境因素对于底泥磷释放的影响。