烟气脱硝催化剂的回收利用工艺

随着国家对氮氧化物排放的控制越来越严格,选择性催化还原（SCR）烟气脱硝技术在燃煤电厂脱硝工程中被广泛应用。文章介绍了我国烟气脱硝催化剂的产生及回收利用情况,并对现有的回收利用工艺进行了分析,重点介绍了一种可促进烟气脱硝催化剂资源利用最大化、避免造成二次环境污染的脱硝催化剂回收利用工艺。     

不同乙酸钠/甘油比对好氧/延长闲置SBR除磷性能的影响

以合成废水为研究对象,以甘油和生活污水中常见的乙酸钠作为碳源,建立了5个好氧/延长闲置序批式反应器(乙酸钠/甘油比分别为1∶0、4∶1、1∶1、1∶4和0∶1),考察了各反应器长期运行过程中的除磷效果,并通过分析典型周期内磷及微生物体内各储能物质的变化,初步探究不同乙酸钠/甘油比对除磷性能的影响机理.研究表明,当乙酸钠/甘油比由1∶0逐渐降至4∶1和1∶1时,平均除磷率由90.1%升至92.5%、97.3%.乙酸钠/甘油比继续降至1∶4及0∶1时,系统除磷率降至65.7%、53.4%.当乙酸钠/甘油比为1∶1时,聚磷菌体内合成大量聚羟基脂肪酸酯(PHAs)(2.55 mmol·g-1,以每g VSS积累的C(mmol)计,下同),为后续磷的吸收及聚磷合成提供更多的能量,而以甘油作为单一碳源时,PHAs合成量最少(0.82 mmol·g-1),糖原合成量最大(2.56 mmol·g-1,以每g VSS积累的C(mmol)计).     

溶解氧对好氧/延长闲置SBR除磷性能的影响

以合成废水为研究对象,乙酸钠为外加碳源,考察不同溶解氧(DO)浓度下好氧/延长闲置(O/EI)序批式反应器的除磷效果,并通过分析典型周期内磷元素及微生物体内各储能物质的变化,探究DO浓度对O/EI工艺除磷性能的影响机制.结果表明,低DO浓度(1 mg·L-1)条件下,O/EI系统具有良好的除磷效果,除磷率高达96%,单位污泥除磷量为5.02 mg·g-1;而当DO浓度较高(4 mg·L-1)时,反应器内磷的去除率降至50%,单位污泥除磷量仅2.81 mg·g-1.研究表明,在DO浓度为1 mg·L-1时,微生物能合成较多聚羟基脂肪酸酯(PHAs),糖原的合成及利用较少,系统好氧吸磷量远高于其他反应器,并在闲置期释放出更多聚磷酸盐.可见,DO可通过影响微生物体内PHAs和糖原的合成及转化,闲置期释磷,好氧前期释磷及好氧吸磷,进而影响系统的除磷性能.     

Water treatment sludge for phosphate removal from the effluent of UASB reactor treating municipal wastewater

Aluminium-based water treatment sludge was used as a coagulant for removing/recovering phosphate from the effluent of upflow anaerobic sludge blanket (UASB) reactor treating municipal wastewater. The effect of three variables, namely sludge dose, initial pH and fresh coagulant (poly-aluminium chloride, PACl) dose was studied using response surface methodology. About 87% phosphate removal could be obtained at the optimum conditions of sludge dose 13.8 g/L, initial pH 6, and fresh PACl dose 5.8 mg Al/L. In order to achieve a similar phosphate removal, a dose in the range of 30–40 mg Al/L of fresh PACl was required. The results suggest that water treatment sludge can be reused as a coagulant for post-treatment of UASB reactor effluent treating municipal wastewater and can be considered as a promising alternative for removing phosphate which can substantially reduce the consumption of fresh PACl. The sludge generated during this process could potentially be used in land application which results in recycling of phosphate.     

Steel slag carbonation in a flow-through reactor system: The role of fluid-flux

Steel production is currently the largest industrial source of atmospheric CO₂. As annual steel production continues to grow, the need for effective methods of reducing its carbon footprint increases correspondingly. The carbonation of the calcium-bearing phases in steel slag generated during basic oxygen furnace (BOF) steel production, in particular its major constituent, larnite {Ca₂SiO₄}, which is a structural analogue of olivine {(MgFe)₂SiO₄}, the main mineral subjected to natural carbonation in peridotites, offers the potential to offset some of these emissions. However, the controls on the nature and efficiency of steel slag carbonation are yet to be completely understood. Experiments were conducted exposing steel slag grains to a CO₂-H₂O mixture in both batch and flow-through reactors to investigate the impact of temperature, fluid flux, and reaction gradient on the dissolution and carbonation of steel slag. The results of these experiments show that dissolution and carbonation of BOF steel slag are more efficient in a flow-through reactor than in the batch reactors used in most previous studies. Moreover, they show that fluid flux needs to be optimized in addition to grain size, pressure, and temperature, in order to maximize the efficiency of carbonation. Based on these results, a two-stage reactor consisting of a high and a low fluid-flux chamber is proposed for CO₂ sequestration by steel slag carbonation, allowing dissolution of the slag and precipitation of calcium carbonate to occur within a single flow-through system.     

Effect of water vapor on NH3-NO/NO2 SCR performance of fresh and aged MnOx-NbOx-CeO2 catalysts

A MnOx–NbOx–CeO2 catalyst for low temperature selective catalytic reduction(SCR) of NOx with NH3 was prepared by a sol–gel method, and characterized by NH3–NO/NO2 SCR catalytic activity, NO/NH3 oxidation activity, NOx/NH3 TPD, XRD, BET, H2-TPR and in-situ Diffuse Reflectance Infrared Fourier Transform Spectroscopy(DRIFTS). The results indicate that the Mn Ox–Nb Ox–CeO2 catalyst shows excellent low temperature NH3-SCR activity in the temperature range of 150–300℃. Water vapor inhibits the low temperature activity of the catalyst in standard SCR due to the inhibition of NOx adsorption. As the NO2 content increases in the feed, water vapor does not affect the activity in NO2 SCR. Meanwhile, water vapor significantly enhances the N2 selectivity of the fresh and the aged catalysts due to its inhibition of the decomposition of NH4NO3 into N2O.     

SBBR处理腈纶生产废水的实验研究

二甲基乙酰胺湿纺腈纶废水是含有难降解物质的化工废水,碳氮比低,水质波动大。采用序批式生物膜反应器对二甲基乙酰胺湿纺腈纶废水进行实验研究,结果表明:在工艺参数为曝气时间3 h,溶解氧4.5~5.5 mg/L,补充无机碳源碳酸氢钠0.5 mg/L,缺氧停留时间2 h的工况下,COD去处理率为75%,BOD为98%,TOC为70%,NH4+-N为94%,TN为80%,DMAC达到99%。     

上推流厌氧反应器连续干发酵猪粪产沼气试验研究

为解决猪粪连续干发酵存在的氨抑制和出料难等难题,在温度(25±2)℃、有机负荷为干物质(TS)4.44 g.(L.d)-1的条件下,采用上推流式厌氧反应器(UPAR)对猪粪进行连续干式发酵试验,研究了猪粪干发酵过程的产气情况、氨抑制现象和出料流动性,并考察了上推流厌氧反应器进行猪粪干发酵的可行性.试验采用4种不同TS质量分数(20%、25%、30%、35%)的猪粪作为原料,经160 d的运行.结果表明,进料TS质量分数对发酵过程有很大的影响,4种不同进料TS质量分数稳定的池容产气率分别为2.40、1.73、0.89、0.62 L.(L.d)-1,进料TS质量分数为20%、25%和30%的产气效率明显优于进料TS=35%的产气效率.随着进料TS质量分数从20%增加到35%,氨氮质量浓度>2 300 mg.L-1会出现明显的产气抑制.在进料TS=35%时,氨氮质量浓度能达到3 800 mg.L-1,产气速率相对于进料TS=20%递减74.1%.当进料TS达到35%、出料TS质量分数达到17.1%、流速<0.002 m.s-1时,UPAR不能顺利出料.     

SBR双颗粒污泥系统脱氮除磷性能研究

以模拟废水为研究对象,对SBR双颗粒污泥系统的脱氮除磷性能进行了考察.试验结果表明,A₂N双颗粒污泥系统能使硝化菌和聚磷菌分别在各自最佳的环境中生长,有利于系统脱氮除磷的稳定和高效运行,可控制性也得到了提高.在COD为300 mg·L^-1条件下,系统对COD的平均去除率达到78.8%,大部分COD被聚磷菌用来合成PHA;当溶解氧控制在3.55~4.90 mg·L^-1和5.60~6.60 mg·L^-1之间时,硝化SBR对氨氮的去除率分别为87.0%和94.5%.除磷SBR仅设置缺氧段时,磷去除率为72%;增设后曝气段后,磷去除率增至85%.NO_x^--N(NO₂^--N+ NO₃^--N)的去除主要发生在缺氧段,在反硝化除磷时作为电子受体被去除,平均去除率为90.6%.     

A novel method to synthesize polyaluminum chloride with a membrane reactor

Al13 or Alb is usually regarded as the most efficient species of polyaluminum chloride(PAC), the performance flocculant for water treatment. This paper was intended to report a new method to synthesize PAC with high content Alb, by using the membrane reactor. NaOH solutions were managed to permeate slowly through the micropores of ultrafiltration membrane into AlCl3 solutions under the suitable transmembrane pressure(TMP). Meanwhile NaOH drops size was limited to nano-scale, resulting in dramatical reduction of the characteristic diffusion time and great increment of contact interface between the strong base and AI ions in solution to favor the formation of Al(OH)4^-, the precursor of AI,3, so few precipitates and much Alb are produced. When the initial concentration of AlCl3/NaOH is 0.40/2.0 (mol/L), MWCO = 10000, TMP = 0.0085 MPa, T= 305 K and B(molar ratio of OH^-/Al^3 ) = 2.25, the quantity of Alb attains about 80%. The results of ^27Al-NMR determination showed that the Al13 content is equal to Alb content. And our PAC product has shown better flocculation effects than the commercial product.