响应面法优化MAP沉淀去除回收尿液中磷的研究

基于模拟尿液的组成特点,利用Box-Behnken Design实验及响应面法对磷酸铵镁(MAP)沉淀去除回收尿液磷过程中反应pH值、Mg²⁺与PO₄^3-物质的量比(Mg/P比)及Ca²⁺与PO₄^3-物质的量比(Ca/P比)3个重要影响因素(分别表示为X₁、X₂、X₃)及各因素之间的交互式影响进行考察,并利用SEM、FTIR、ICP和XRD表征手段分析结晶沉淀组成和晶形特征.实验结果表明,回归方程中X₁、X₂、X₃、X₁X₃、X₂X₃、X₁²、X²₂、X₃²对磷去除率影响显著;当反应pH值和Mg/P比范围分别在8.5~9.5和1.0~1.2之间时,磷去除率响应值能达到99%.产物表征结果表明,模拟尿液中K⁺和Na⁺对结晶干扰较小;当Ca²⁺的浓度相对较低(Ca/P比小于0.25)时,沉淀中MAP的纯度高于85%,晶体形状大部分为斜方形;当Ca²⁺的浓度相对较高(Ca/P比大于0.25)时,沉淀中的MAP下降明显,晶体形状开始不规则,杂质增多;当模拟尿液中Ca/P比为0.5时,MAP纯度仅有约70%.     

Tetrahedral homonuclear organoelement clusters and subhalides of aluminium,gallium and indium

This review is focused on the synthesis and the reactivity of tetrahedral organoelement clusters of the heavier elements of third main-group aluminium, gallium, and indium, which have been known for about a decade. They possess the elements in an unusually low oxidation state of +1 and have direct element–element interactions between their four constituents. Each cluster atom is further attached to one terminal and in most cases a bulky organic substituent, which prevents disproportionation by steric shielding. The synthesis of these compounds succeeds by different methods such as the reduction of suitable organoelement(III) halides with alkali metals and magnesium or the treatment of element(I) halides with lithium organyls. They are deeply coloured, and their bonding situation may best be described by delocalized molecular orbitals. They show a singular chemical reactivity, which results in the formation of many secondary products possessing unprecedented structures and properties. The synthesis of organoelement subhalides still containing the elements in low oxidation states is discussed in more detail in the second part of this review. These compounds are easily accessible by the careful oxidation of the clusters with halogen donors such as hexachloroethane or with AlX₃/X₂ mixtures. They produce dimers via halogen bridges, but in certain cases monomers were observed even for the solid state. They are very effective starting compounds for secondary reactions and the generation of new products containing the elements in unusual oxidation states by salt-elimination reactions, for instance.     

培养转速与镁离子对生物合成次生铁矿物的影响研究

探析培养转速与镁离子浓度对氧化亚铁硫杆菌生物合成次生铁矿物的影响对酸性矿山废水(AMD)治理具有一定的工程指导意义.本研究通过摇瓶实验,研究了Mg2+浓度分别为48与4.8 mg·L-1,其它元素组成与富含Fe与SO2-4的9K液体培养基一致的体系在180 r·min-1与100 r·min-1转速条件下氧化亚铁硫杆菌催化合成次生铁矿物过程.考察了不同次生铁矿物合成体系pH、Fe2+氧化率、总Fe沉淀率及次生铁矿物矿相等相关指标.研究结果表明,在180 r·min-1的培养条件下,Mg2+浓度分别为4.8与48 mg·L-1两体系培养48 h后,pH从原始的2.50分别降低至2.07与2.12,Fe2+均可在48 h内实现完全氧化.Fe2+完全氧化时,Mg2+浓度为4.8 mg·L-1体系总Fe沉淀率为37.4%,合成的次生铁矿物均匀分散于溶液中,而Mg2+浓度为48 mg·L-1体系中,总铁沉淀率仅为31.7%,且70%的矿物牢固粘附于摇瓶底部.培养转速为100 r·min-1时,Mg2+浓度分别为4.8与48 mg·L-1两体系经过72 h培养后,pH均从原始的2.50降低至2.21与2.17.Fe2+需要72 h才能被完全氧化,两体系总Fe沉淀率分别仅为21.3%与23.0%,产生的次生铁矿物几乎全部牢固粘附于摇瓶底部.本研究所有体系产生的次生铁矿物均为黄铁矾与施氏矿物的混合物.研究结果可为生物合成次生铁矿物工艺的优化及其在酸性矿山废水治理领域的有效应用提供必要的参数支撑.     

缺镁胁迫对普通小球藻光合生理及油脂积累的影响

小球藻是一种重要的生物资源,它在生产微藻燃料、提取生物活性物质以及水环境修复等方面具有广阔的应用,因此研究小球藻的生理生化特性具有重要的意义.镁离子在微藻的生长过程中起到了很重要的作用,不仅是叶绿素结构的中心原子,还是一些代谢途径中关键酶的辅因子.采用批次培养的方法,在对普通小球藻(Chlorella vulgaris)光合自养培养过程中,研究了在缺镁胁迫条件下的普通小球藻的光合生理及油脂积累的变化.结果表明,在缺镁胁迫条件下,普通小球藻的生物量、蛋白含量、叶绿素a含量、叶绿素b含量分别降低了20%、43.96%、27.52%、28.07%,而总油脂含量增加了19.60%;普通小球藻的最大光能转化效率Fv/Fm降低了22.54%,而非光化学淬灭qN显著高于正常培养条件.本研究结果表明缺镁胁迫抑制了普通小球藻中叶绿素的合成,从而影响了光合作用的进行,导致普通小球藻生长受到抑制、蛋白质合成受阻,从而使其碳同化进入油脂的合成代谢,增加了普通小球藻油脂含量.     

Sulfobacillus benefaciens强化中度嗜热菌群浸出铅锌硫化矿尾矿过程机制

针对铅锌硫化矿尾矿生物浸出周期长和效率低的问题,本研究采用Leptospirillum ferriphilum（L. ferriphilum）和Acidithiobacillus caldus（A. caldus）等比例混合构建了中度嗜热菌群,浸出铅锌硫化矿尾矿.引入一株兼性自养铁/硫氧化微生物Sulfobacillus benefaciens（S. benefaciens）,考察其对中度嗜热菌群浸出尾矿过程的影响.结果表明,中度嗜热菌群（L. ferriphilum+A. caldus）8 d Zn浸出率达到93.94%.随着S. benefaciens引入,浸出环境保持更高的氧化还原电位和微生物活性,浸出过程中Fe³⁺浓度以及总铁浓度增加,4 d内Zn浸出速率提升了13.63%,8 d内Zn浸出率达到96.08%,S. benefaciens的加入强化了中等嗜热菌群的浸出效率.相关性分析表明多糖、蛋白质以及溶解性有机碳（DOC）与浸出过程中的溶液介质参数变化具有统计学意义上显著性和强相关性.表面官能团以及胞外聚合物（EPS）结果证实,引入S. benefaciens在浸出过程中促进菌群产生更多的蛋白质和碳水化合物,有助于提高中度嗜热菌群的浸出效率,加快浸出铅锌硫化矿尾矿中有价金属,降低其环境毒性.     

Heterogeneous sulfur conversion in sea-salt aerosol particles: the role of aerosol water content and size distribution

Meteorological and chemical conditions during the July 1988 Bermuda-area sampling appear to have been favorable for conversion of sulfur gases to particulate excess sulfate (XSO₄). Observed average XSO₄ and SO₄ concentrations of 11 and 2.1 nmol m⁻³, respectively, at 15 m a.s.l. in the marine boundary layer (MBL) upwind of Bermuda, indicate that conversion of SO₂ to XSO₄, over and above homogeneous conversion, may be necessary to explain the > 5.0 average molar ratio of XSO₄ to SO₂. Given an observed cloud cover of <15% over the region and the <3 nmol m⁻³ SO₃ concentrations observed by aircraft, heterogeneous conversion mechanisms, in addition to cloud conversion of SO₂, are necessary to explain the observed 11 nmol XSO₄ m⁻³.Aerosol water content, estimated as a function of particle size distribution plus consideration of SO₂ mass transfer for the observed particle size distribution, shows that SO₂ was rapidly transferred to the sea-salt aerosol particles. Assuming that aqueous-phase SO₂ reaction kinetics within the high pH sea-salt aerosol water are controlled by O₃ oxidation, and considering mass-transfer limitations, SO₂ conversion to XSO₄ in the sea-salt aerosol water occurred at rates of approximately 5% h⁻¹ under the low SO₂ concentration, Bermuda-area sampling conditions. All of the 2 nmol XSO₄ m⁻³ associated with sea-salt aerosol particles during low-wind-speed, Bermuda-area sampling can be explained by this conversion mechanism. Higher wind speed, greater aerosol water content and higher SO₂ concentration conditions over the North Atlantic are estimated to generate more than 4 nmol XSO₄ m⁻³ by heterogeneous conversion of SO₂ in sea-salt aerosol particles.     

Physiological responses and detoxific mechanisms to Pb, Zn, Cu and Cd in young seedlings of Paulownia fortunei

Paulownia fortunei has been successfully used in the phytoremediation of many Pb/Zn mine tailings. However, seed germination and young seedlings of P. fortunei rarely occurred in these mine tailings. The physiological responses and detoxific mechanisms of P. fortunei young seedling to Pb, Zn, Cu and Cd stress were investigated. The germinated rate, shoot length, chlorophyll and carotenoid contents in leaves of young seedlings had a great reduction under Zn and Cu treatments, but had little decrease under Pb and Cd treatments. The production rate of O₂^•−, H₂O₂ and malondialdehyde (MDA) contents significantly increased in response to added Zn and Cu indicating great oxidative stress for young seedlings, but they had no significant change to added Pb and Cd. Young seedlings had effective detoxific mechanism to Pb and Cd, as antioxidant enzymes activities, phytochelatins (PCs-SH) and proline contents increased with increasing rates of added Pb and Cd. However, young seedlings had un-effective detoxific mechanisms to Zn and Cu stress. Results revealed the heavy metals (such as Cu) that present at low concentrations in mine tailings may be major constraint for the survival of young seedlings.     

北京市密云水库上游金铁矿区土壤重金属污染特征及对比研究

不同金属矿山选冶活动造成的矿区及周边土壤中重金属的分布累积特征不同.为了解密云水库上游金矿和铁矿矿区土壤中重金属地球化学特征的异同及污染状况,对区域内典型的金矿和铁矿矿区进行土壤样品采集,应用地球化学方法研究了2种土壤中重金属的污染特征,并应用地累积指数法评价了其污染状况.结果表明,2种土壤中除As外的其它重金属含量明显高于北京市土壤重金属背景值,金矿矿区土壤重金属含量普遍高于铁矿矿区.相关性分析表明,金矿矿区土壤中Cu含量与Pb、Zn(p<0.01)及Cr、有机质(OM)含量(p<0.05)之间显著相关,pH值与Pb含量(p<0.01)及Hg含量(p<0.05)呈显著负相关,而铁矿矿区土壤中重金属含量之间的相关性不显著.金矿尾砂中重金属含量明显高于铁矿尾砂,与矿区土壤污染状况一致.地累积指数法评价结果显示,金铁矿区土壤中重金属的污染程度均已十分严重,金矿矿区土壤污染程度高于铁矿,金矿矿区土壤重金属的污染程度由高到低依次为:Pb>Hg>Cd>Cr>Cu>Zn>Co>As;铁矿矿区土壤重金属的污染程度由高到低依次为:Pb>Cd>Cr>Co>Cu>Zn>Hg>As.该研究数据可为同一区域内不同金属矿区重金属污染的有效监控与治理提供科学依据.     

黄河口不同恢复阶段湿地土壤N2O产生的不同过程及贡献

采用时空替代法,选择黄河口生态恢复前后未恢复区(R0)、2007年恢复区(R2007)和2002年恢复区(R2002)的芦苇湿地为研究对象,分析了生态恢复工程对湿地土壤N2O产生不同过程与贡献的影响.结果表明,尽管不同恢复阶段湿地土壤N2O总产生量差异明显,但总体均表现为N2O释放.恢复区湿地土壤的N2O产生量大于未恢复区.N2O的产生主要以硝化作用和硝化细菌反硝化作用为主,而反硝化作用对N2O的产生有较大削弱作用,这与不同恢复阶段湿地土壤理化性质密切相关.非生物作用对N2O产生量贡献较大,这与黄河口为高活性铁区,Fe的还原作用关系密切.尽管黄河口不同恢复阶段湿地土壤N2O的产生是生物作用与非生物作用共同作用的结果,但由于非生物作用对N2O产生的影响较大,应受到特别关注.温度和水分对不同恢复阶段湿地土壤N2O产生过程的影响不尽一致,这与土壤微生物活性对温度和水分的响应差异有关.黄河口不同恢复阶段湿地土壤的N2O总产生量介于(0.37±0.08)～(9.75±7.64)nmol·(kg·h)-1,略高于闽江口互花米草湿地的N2O总产生量,但明显低于富氧森林土壤、草原土壤和闽江口短叶茳芏湿地的N2O总产生量.研究发现,黄河口生态恢复工程的长期实施明显促进了N2O的产生,因而下一步生态恢复工程应统筹考虑景观恢复与温室气体削弱这两方面因素.     

蒽醌类有机质对针铁矿异化还原解离特征影响

基于希瓦氏金属还原菌(Shewanella decolorationis S12)和针铁矿相互作用,讨论了蒽醌类有机质(AQS)对该针铁矿异化还原过程的调控机制.结果表明:AQS作为电子运移载体,使得还原解离态铁总量(Fetot)和可溶态铁含量(Fedis)均快速增加;不同含量的AQS加入前后,针铁矿还原平均速率得到显著上升,速率比在2.4~4.0之间,且该比值和AQS含量呈显著的线性关系,可决系数为0.9947.Fedis/Fetot比值随AQS含量升高而降低,当AQS含量由0.05 mmol·L-1增加至0.3 mmol·L-1时,Fedis/Fetot比值由0.935减小至0.705.Feads含量随AQS含量增加而增加,当体系中无AQS时,Feads含量维持在较低的水平(0.05 mmol·L-1).AQS参与下的铁异化还原过程实际上是由两个独立的子过程组成,即微生物呼吸作用驱动了AQS和还原态蒽二酚(AH2QS)的循环转变过程以及AH2QS进一步还原解离针铁矿的非生物过程.     

Mechanism of Methylene Blue adsorption on hybrid laponite-multi-walled carbon nanotube particles

The kinetics of adsorption and parameters of equilibrium adsorption of Methylene Blue(MB)on hybrid laponite-multi-walled carbon nanotube(NT)particles in aqueous suspensions were determined.The laponite platelets were used in order to facilitate disaggregation of NTs in aqueous suspensions and enhance the adsorption capacity of hybrid particles for MB.Experiments were performed at room temperature(298 K),and the laponite/NT ratio(X_l)was varied in the range of 0–0.5.For elucidation of the mechanism of MB adsorption on hybrid particles,the electrical conductivity of the system as well as the electrokinetic potential of laponite-NT hybrid particles were measured.Three different stages in the kinetics of adsorption of MB on the surface of NTs or hybrid laponite-NT particles were discovered to be a fast initial stage Ⅰ(adsorption time t=0–10 min),a slower intermediate stage Ⅱ(up to t=120 min)and a long-lasting final stage Ⅲ(up to t=24 hr).The presence of these stages was explained accounting for different types of interactions between MB and adsorbent particles,as well as for the changes in the structure of aggregates of NT particles and the long-range processes of restructuring of laponite platelets on the surface of NTs.The analysis of experimental data on specific surface area versus the value of X_l evidenced in favor of the model with linear contacts between rigid laponite platelets and NTs.It was also concluded that electrostatic interactions control the first stage of adsorption at low MB concentrations.     

Oxidation of organic substances in aqueous solutions over Ru catalysts by oxygen

The catalytic performance of supported Ru catalysts has been studied in the reactions of wet oxidation of acetonitrile, N,N-dimethyl formamide and carbamide at T=433–533 K and P=2.0–4.6 MPa, and wet oxidation of real sewage from an alcohol plant (so-called Luther water) at T=403–473 K and P=1.5–3.6 MPa. The Luther water contained a mixture of low-boiling (C₁–C₅) aldehydes and alcohols. The experiments were carried out in a perfectly mixed batch autoclave reactor. The conversion of alcohols and aldehydes contained in the Luther water and selectivity of the process towards CO₂ and water as well as the selectivity of the oxidation of acetonitrile, N,N-dimethyl formamide and carbamide towards CO₂, N₂ and water were determined at various temperatures and reaction times. Ru (4.8 wt.%)/graphite-like carbon was effective in the oxidation of Luther water (ΔTOC=97.5% at T=423 K for 1 h), carbamide (X_CO(NH2)2=100%, S_{CO(NH2)2→CO2}=100%, S_{CO(NH2)2→N2}=71% at 473 K, 2 h) and acetonitrile (X_CH3CN=100%, S_CH3CN→CO2=100%, S_CH3CN→N2=75% at 493 K, 1 h). Ru/active carbon/γ-Al₂O₃ was effective in the oxidation of N,N-dimethyl formamide (X_HCON(CH3)2=100%, S_{HCON(CH3)2→CO2}=61%, S_{HCON(CH3)2→N2}=100% at 493 K).     

反应气氛对绿色合成纳米铁的组分及其活性的影响

成本低廉和无二次污染的"绿色"合成纳米材料是发展原位纳米环境修复技术的前沿研究课题之一.本文以绿茶提取液为还原剂和稳定剂进行"绿色"合成纳米铁,探讨在不同的气氛下"绿色"合成的纳米铁颗粒的主要成分,以期为调控合成纳米铁系材料提供基础研究.首先,利用扫描电子显微镜(SEM)、X射线能谱(EDS)、X射线光电子能谱分析(XPS)和傅里叶变换红外光谱(FTIR)等表征手段对不同反应气氛下合成的纳米铁颗粒的表面微观形貌、尺寸和价态结构进行分析.结果发现,在通入N2情况下,合成的纳米铁颗粒粒径为(84.7±11.5)nm,其主要成分以纳米零价铁为主;在通入空气情况下,合成的纳米铁粒径为(117.8±26.2)nm,其主要成分是纳米零价铁、氧化铁和四氧化三铁的混合物;通入O2时,合成的纳米铁粒径为(141.2±26.3)nm,其主要成分以四氧化三铁为主.其次,评价在不同气氛条件下合成纳米铁颗粒对去除亚甲基蓝(MB)的反应活性.结果表明,在反应温度313 K下降解初始浓度为50 mg·L-1的MB溶液,反应5 min时已达到平衡,通入N2合成的纳米铁降解MB,去除率高达98.7%,而通入O2合成的纳米铁反应效率低,对MB的去除率仅为65.3%.最后,从以上发现提出不同气氛下可以调控"绿色"合成的铁系纳米材料成分,从而导致不同的纳米修复环境中污染物的能力.     

京津冀地区钢铁行业污染物排放清单及对PM2.5影响

以京津冀地区为研究区域,采取自下而上的方法,建立京津冀地区钢铁行业细化至焦化、烧结和球团、炼铁、炼钢、轧钢等工序的多污染物排放清单.清单估算结果显示,2015年京津冀地区钢铁行业SO₂、NO_x、TSP、PM₁₀、PM_2.5、CO、VOC的排放量分别为38.82、27.23、79.19、53.15、38.68、823.38、26.53万t,其中烧结和球团工序是最主要的污染物排放工序（17.0%~72.0%）,其次为炼铁工序（4.6%~42.4%）和轧钢工序（3.5%~35.7%）.采用具有污染物来源示踪功能的双层嵌套气象-空气质量模型系统（WRF-CAMx）耦合模型模拟京津冀地区钢铁行业污染物排放对区域大气PM_2.5浓度的影响.模拟结果显示：钢铁行业在春夏秋冬这4个季节对京津冀地区PM_2.5浓度贡献率分别达到14.0%、15.9%、12.3%、8.7%.各地市中,钢铁行业对唐山市PM_2.5影响最大,年均PM_2.5浓度贡献率高达41.2%,其次为秦皇岛市、石家庄市、邯郸市,年均PM_2.5浓度贡献率分别达到19.3%、15.3%、15.1%.     

矿业废弃地重金属形态分布特征与迁移转化影响机制分析

为探究矿业废弃地重金属形态分布特征和迁移转化的影响机制,在广东大宝山矿区矿业废弃地采集土壤和尾砂样品,分析重金属形态特征;采用Pb稳定同位素分析进行矿区污染源解析,并结合矿区典型矿物的X射线衍射分析(XRD)、透射电镜-能谱分析(TEM-EDS)和拉曼分析,以及室内模拟浸出实验,阐明矿区重金属迁移转化的特征和影响因素.结果表明,矿区土壤和沉积物样品中Cd、 Pb和As的赋存形态以残渣态为主,占总量的比例范围为85%～95%;其次为铁锰氧化物结合态(1%～15%).矿区土壤和尾砂中的主要矿物类型为黄铁矿(FeS₂)、黄铜矿(CuFeS₂)和金属氧化物,同时也存在少量的闪锌矿(ZnS)和方铅矿(PbS).酸性条件(pH=3.0)有利于Cd和Pb从土壤、尾砂和矿物(黄铁矿和黄铜矿)中释放迁移,并从残渣态向非残渣态转化.铅同位素分析显示土壤和尾砂中的重金属(Pb)主要来自采矿区金属矿物的释放,矿区柴油的贡献率在30%以内.多元统计分析表明矿区土壤和尾砂重金属主要来源于3种类型的矿物污染源,即黄铁矿、黄铜矿和闪锌矿+金属氧化物,其中Cd、 As和Pb主...     

镁铁复合絮凝剂的表征及应用研究

以FeSO4、MgO和H2SO4为原料,制备了新型镁铁复合絮凝剂(PFMS),考察了PFMS的结构和Fe(Ⅲ)分布形态,为了考察自制PFMS、自制聚合硫酸铁(PFS)与工业PFS产品的絮凝性能差别,选择高岭土模拟浊度废水、直接耐晒黑G模拟染料废水和焦化废水生化出水,分别进行了去除浊度、色度和COD的絮凝实验.结果表明,Mg2+未参与聚合过程,但引入Mg2+提高了PFMS的稳定性.PFMS对浊度去除效果略高于自制PFS和工业PFS,余浊<5NTU;在碱性条件下,PFMS的脱色率、COD去除率高于自制PFS和工业PFS.     

Biogenic cements and encapsulation of zinc

Metals can be stabilized into cement matrix by solidification/stabilization process. Rice hull is an agricultural residue containing about 10-20% (weight) of silica. It can be used to synthesize β-Ca₂SiO₄, an important component of Portland cement. Furthermore it is possible to prepare β-Ca₂SiO₄ doped with heavy metals. Here we describe the synthesis of β-Ca₂SiO₄ doped with zinc and the behavior of mortars prepared using this material. Products were analyzed by X-ray diffraction, differential thermal analysis and scanning electron microscopy coupled to energy-dispersive spectroscopy. The maximum amount of zinc that can be inserted into β-Ca₂SiO₄, without affecting the crystalline structure, is limited to 2% (molar basis). In comparison with conventional mortars, zinc-modified mortars show a similar behavior, regarding porosity, resistance to acidic attack and compressive strength. The synthesis of β-Ca₂SiO₄ doped with zinc presents a new possibility for safety enhancement in solidification/stabilization processes.     

Trace gas emissions from tropical biomass fires: Yucatan Peninsula,Mexico

Mixing ratios for carbon dioxide (CO₂), carbon monoxide (CO), hydrogen (H₂), methane (CH₄) and total non-methane hydrocarbons (TNMHC) were determined from the smoke plumes of two small (∼0.25 ha) prescribed biomass fires conducted on the Yucatan Peninsula in Mexico. In the region of these fires the combination of climate and shallow soils produces a scrubby and stunted forest with species composition similar to the Brazilian rain forest, but at a noticeably reduced size. Aircraft collections of smoke from these fires were analysed and used to determine CO₂-normalized emission ratios (ΔX/ΔCO₂; v/v; where Δ = in-plume specie concentration less background concentration) for CO, H₂, CH₄ and TNMHC produced and released into the atmosphere from these fires. Suprisingly, high mean emission ratios for TNMHCs (∼1.7% of CO₂ release) and H₂ (∼2.5% of CO₂) were determined. Emission ratios for CO (∼7%) and CH₄ (∼0.7%), however, were found to fall within expected bounds.     

基于活性污泥模型的污水COD组分划分方案研究

活性污泥数学模型(ASM)在污水处理厂的成功应用与进水组分的正确划分密切相关.从标准化和定量化的角度利用3个批式试验开发了COD组分划分方案及Matlab计算程序.该方案在上海2个污水处理厂的测定结果表明,曲阳污水厂进水COD中含有8.1%±1.6%的易生物降解组分SS、6.3%±2.2%的溶解性惰性组分SI、45.5%±3.5%的慢速生物降解组分XS、31.1%±2.1%的颗粒性惰性组分XI和9.0%±1.1%的异养菌组分XH.而白龙港污水厂进水COD中含有11.1%±2.2%的SS、9.9%±2.0%的SI、38.9%±10.7%的XS、23.3%±9.8%的XI和16.9%±1.8%的XH.与曲阳污水厂相比,白龙港污水厂进水COD中XS和XI含量偏低,而XH/COD值则明显偏高,表明长距离管道输送会显著影响COD组分浓度.     

Multi-process and multi-pollutant control technology for ultra-low emissions in the iron and steel industry

The iron and steel industry is not only an important foundation of the national economy, but also the largest source of industrial air pollution. Due to the current status of emissions in the iron and steel industry, ultra-low pollutant emission control technology has been researched and developed. Liquid-phase proportion control technology has been developed for magnesian fluxed pellets, and a blast furnace smelting demonstration project has been established to use a high proportion of fluxed pellets (80%) for the first time in China to realize source emission reduction of SO₂ and NO_x. Based on the characteristics of high NO_x concentrations and the coexistence of multiple pollutants in coke oven flue gas, low-NO_x combustion coupled with multi-pollutant cooperative control technology with activated carbon was developed to achieve efficient removal of multiple pollutants and resource utilization of sulfur. Based on the characteristics of co-existing multiple pollutants in pellet flue gas, selective non-catalytic reduction (SNCR) coupled with ozone oxidation and spray drying adsorption (SDA) was developed, which significantly reduces the operating cost of the system. In the light of the high humidity and high alkalinity in flue gas, filter materials with high humidity resistance and corrosion resistance were manufactured, and an integrated pre-charged bag dust collector device was developed, which realized ultra-low emission of fine particles and reduced filtration resistance and energy consumption in the system. Through source emission reduction, process control and end-treatment technologies, five demonstration projects were built, providing a full set of technical solutions for ultra-low emissions of dust, SO₂, NO_x, SO₃, mercury and other pollutants, and offering technical support for the green development of the iron and steel industry.