Inorganic nitrogen removal of toilet wastewater with an airlift external circulation membrane bioreactor

Removal of inorganic nitrogen (inorganic-N) from toilet wastewater, using a pilot-scale airlift external circulation membrane bioreactor (AEC-MBR) was studied. The results showed that the use of AEC-MBR with limited addition of alkaline reagents and volumetric loading rates of inorganic-N of 0.19-0.40 kg inorganic-N/(m3·d) helped achieve the desired nitrification and denitrification. Furthermore, the effects of pH and dissolved oxygen (DO) on inorganic-N removal were examined. Under the condition of MLSS at 1.56-2.35 g/L, BOD5/ammonia nitrogen (NH/-N) at 1.0, pH at 7.0-7.5, and DO at 1.0-2.0 mg/L, the removal efficiencies of NH4 -N and inorganic-N were 91.5% and 70.0%, respectively, in the AEC-MBR. The cost of addition of alkaline reagent was approximately 0.5-1.5 RMB yuan/m3, and the energy consumption was approximately 0.72 kWh/m3 at the flux of 8 L/(m2·h).     

Effects of metal cations on sorption-desorption of p-nitrophenol onto wheat ash

The mutual e ects of metal cations (Cu2+, Pb2+, Zn2+, and Cd2+) and p-nitrophenol (NP) on their adsorption desorption behavior onto wheat ash were studied. Results suggested that Cu2+, Pb2+, and Zn2+ diminished the adsorption and increased the desorption of NP remarkably, while Cd2+ had no such e ect. In contrast, NP diminished the adsorption of Cu2+, Pb2+, and Zn2+ onto ash, however, this suppression e ect depended on the initial concentrations of metal cations. NP had no e ect on Cd2+ adsorption on ash. Fourier transform infrared (FT-IR) and X-ray absorption spectroscopic (XAS) studies suggested the following mechanisms responsible for the metal suppression e ect on NP adsorption: (1) large hydrated Cu2+, Pb2+, and Zn2+ shells occupied the surface of ash and prevent nonspecific adsorption of NP onto ash surface; (2) Cu2+, Pb2+, and Zn2+ may block the micropores of ash, resulting in decreased adsorption of NP; (3) complexation of Cu2+, Pb2+, and Zn2+ was likely via carboxyl, hydroxylic and phenolic groups of wheat ash and these same groups may also react with NP during adsorption. As a “soft acid”, Cd2+ is less e cient in the complexation of oxygencontaining acid groups than Cu2+, Pb2+, and Zn2+. Thus, Cd2+ had no e ect on the adsorption of NP on wheat ash.     

微波酸活化粉煤灰吸附酸性大红染料废水实验研究

以微波酸活化改性后的粉煤灰为吸附剂,对酸性大红染料废水进行吸附脱色处理,考察了吸附时间、pH值、吸附剂投加量等对吸附脱色效果的影响。在酸性大红染料溶液初始浓度为100 mg/L、pH=5、活化粉煤灰投加量为10 g/L吸附1 h时,活化粉煤灰对酸性大红的脱色效果较好,去除率可达96%。对实验数据进行相关数学模型拟合,结果表明微波酸活化改性后的粉煤灰吸附去除酸性大红的等温吸附平衡符合Langmuir吸附等温式,改性前后的吸附过程动力学符合准二级吸附动力学模型,线性相关系数良好。     

生活垃圾焚烧飞灰制陶瓷砖表征

为了探索生活垃圾焚烧飞灰资源化利用途径,在对飞灰化学组成及矿物成分分析的基础上,利用飞灰、黄陶土、耐火砂及长石研制陶瓷砖,最佳配比方案为:飞灰20%,黄陶土60%,长石10%,耐火砂10%,分析了最佳配比制品的吸水率、抗压强度、微观结构及水平振荡浸出毒性。结果表明:飞灰属SiO2-Al2O3-金属氧化物体系,主要矿物成分是钙硅酸盐及铝硅酸盐等,可用于制陶瓷砖;最佳配比制品达MU15强度等级,满足抗风化的要求;随煅烧温度的升高,制品结构不断密实化,960℃烧成的制品显示出完全烧结的特点,960~1 000℃烧成的制品中出现明显的晶化、玻璃化过程。最佳配比制品重金属浸出毒性完全达标,重金属的浸出率与坯体相比大大降低。     

免烧粉煤灰陶粒作为BAF填料处理城市污水

以电厂粉煤灰为主要试验原料,辅以外加药剂(水泥、石灰、石膏、水玻璃),经混合、成球、陈化和养护等工序,制得免烧粉煤灰陶粒,并将其作为曝气生物滤池(BAF)工艺的载体填料处理城市污水.待挂膜启动成功后,考察了水力停留时间( HRT)、COD负荷、氨氮负荷对COD和氨氮去除效果的影响.实验结果表明:在温度为18～21℃、气...     

利用铜矿尾砂研制低强度可控性填料

利用铜矿尾砂、粉煤灰、水泥以及加气剂等,混合搅拌成泥浆体,振动成型,制备出低强度可控性填料(CLSM).试验表明:以水泥12.9％、铜矿尾砂(细集料)22.6％、加气剂3.2％、粉煤灰12.9％等工业废弃物,加水48.4％,固液比控制在(14～15):(15～16)之间,制得的CLSM制品,抗压强度0.35～2.00 ...     

粉煤灰对混合染料的吸附性能研究

以燃煤废弃物粉煤灰作为吸附剂,对活性红23和分散蓝56混合染料溶液进行吸附性能研究.实验结果表明:粉煤灰优先吸附离子型的活性染料,混合溶液中对活性红23的吸附能够在30 min达到平衡,而对分散蓝56的吸附则需要150 min才能够达到平衡,吸附动力学符合准二级吸附模型.在弱酸性环境中粉煤灰对分散染料的脱色高于碱性环境...     

垃圾焚烧飞灰中二噁英削减技术研究

二噁英(PCDD/Fs)是多氯代二苯并二噁英和多氯代二苯并呋喃的总称,因具有生物蓄积性、高毒性、难降解等特点而备受关注。垃圾焚烧是二噁英的重要来源,而其中超过50%的二噁英以飞灰形式排出。文章综述了热分解法、光降解法、机械化学法、生物降解法等飞灰二噁英毒性削减技术的国内外研究进展,并在此基础上对飞灰二噁英削减技术研究和管理提出了建议。     

挥发回转窑处置钢丝绳行业污泥的污染物排放研究

通过利用挥发回转窑处置钢丝绳行业污泥的工业化试验,测定了烟气排放参数及污染物排放指标,分析了污泥添加对挥发回转窑烟气排放的影响程度及各项污染物指标之间的相关性。结果表明,污泥添加量18%～22%,对挥发回转窑烟气排放无影响,烟尘、SO2、氮氧化物、Zn、Pb、HCl等各项污染物指标均符合国家控制标准;烟尘排放浓度与Pb、Zn排放浓度呈显著正相关;SO2排放浓度与烟气含氧量、空气过剩系数、排放浓度呈显著负相关。通过控制烟气中烟尘浓度可减少Zn、Pb的排放,在满足SO2排放浓度达标的同时,还应加强工艺供氧量的管理,控制的产生,减少烟气对生产设备的腐蚀。     

粉煤灰基质复合滤料吸附Mn^2＋试验研究

以粉煤灰基质复合滤料为吸附材料,通过单因素和正交实验相结合的实验方法,考察了吸附滤料投加量、吸附时间、原水初始浓度、振荡频率、温度等因素对除锰效果的影响。从单因素实验可知：随着滤料质量的增大,Mn2＋去除率在开始时增长幅度较大,后来逐渐趋于平缓。在正交实验中固定滤料投加量为300 g/L,发现在锰离子的吸附过程中,吸附时间的影响最大,随后分别是原水浓度和温度,振荡频率的影响程度最小。