Red soil as a regenerable sorbent for high temperature removal of hydrogen sulfide from coal gas

In this study, hydrogen sulfide (H(2)S) was removed from coal gas by red soil under high temperature in a fixed-bed reactor. Red soil powders were collected from the northern, center and southern of Taiwan. They were characterized by XRPD, porosity analysis and DCB chemical analysis. Results show that the greater sulfur content of LP red soils is attributed to the higher free iron oxides and suitable sulfidation temperature is around 773K. High temperature has a negative effect for use red soil as a desulfurization sorbent due to thermodynamic limitation in a reduction atmosphere. During 10 cycles of regeneration, after the first cycle the red soil remained stable with a breakthrough time between 31 and 36 min. Hydrogen adversely affects sulfidation reaction, whereas CO exhibits a positive effect due to a water-shift reaction. COS was formed during the sulfidation stage and this was attributed to the reaction of H(2)S and CO. Results of XRPD indicated that, hematite is the dominant active species in fresh red soil and iron sulfide (FeS) is a product of the reaction between hematite and hydrogen sulfide in red soils. The spinel phase FeAl(2)O(4) was found during regeneration, moreover, the amount of free iron oxides decreased after regeneration indicating the some of the free iron oxide formed a spinel phase, further reducting the overall desulfurization efficiency.     

污水厂脱水污泥制吸附剂及脱除H2S效能研究

采用热解炭化法制备了一系列污泥吸附剂,优化制备工艺,利用扫描电镜(SEM)、比表面积和孔径分析等技术对污泥吸附剂的结构进行了表征,并研究了脱除H2S效能。结果表明,活化温度、活化时间和固液比等因素均对污泥吸附剂的碘吸附值产生影响。当活化温度为550℃、活化时间为2.0h、固液比为1∶2时所制备材料(SA)的碘吸附值最高,为493.12mg/g;制备的SA具有较好的脱除H2S效能,能满足精脱硫的要求,当空速为4600h-1时,SA的除臭时间可达48min;此外SA中含有的多种金属元素,平均孔径为3.4nm,这些性质均有利于H2S的吸附脱除。     

Effective heavy metal removal from aqueous systems by thiol functionalized magnetic mesoporous silica

A thiol-functionalized magnetic mesoporous silica material (called SH-mSi@Fe₃O₄), synthesized by a modified Stöber method, has been investigated as a convenient and effective adsorbent for heavy metal ions. Structural characterization by powder X-ray diffraction, N₂ adsorption-desorption isotherm, Fourier transform infrared spectroscopy and elemental analyses confirms the mesoporous structure and the organic moiety content of this adsorbent. The high saturation magnetization (38.4 emu/g) make it easier and faster to be separated from water under a moderate magnetic field. Adsorption kinetics was elucidated by pseudo-second-order kinetic equation and exhibited 3-stage intraparticle diffusion mode. Adsorption isotherms of Hg and Pb fitted well with Langmuir model, exhibiting high adsorption capacity of 260 and 91.5 mg of metal/g of adsorbent, respectively. The distribution coefficients of the tested metal ions between SH-mSi@Fe₃O₄ and different natural water sources (groundwater, lake water, tap water and river water) were above the level of 10⁵ mL/g. The material was very stable in different water matrices, even in strong acid and alkaline solutions. Metal-loaded SH-mSi@Fe₃O₄ was able to regenerate in acid solution under ultrasonication. This novel SH-mSi@Fe₃O₄ is suitable for repeated use in heavy metal removal from different water matrices.     

Distribution of extractable fractions of heavy metals in sludge during the wastewater treatment process

Sludge samples were collected from different treatment steps of Gaobeidian wastewater treatment plant (WWTP) of Beijing City, PR China, to investigate the distributions of total and chemical fractions of Fe, Mn, Ni, Cu, Zn, Cr, Pb, and Mo in different sludges. The highest total concentrations were found for Fe, Mn, Pb, and Mo in digested sludge (DS), Ni and Cr in thickened sludge (TS), Zn in dewatering sludge (DWS), and Cu in active sludge (AS). The lowest concentrations were observed in AS, except for Cu in TS. Significant differences of total metal concentration were observed between AS and TS (or DS), suggesting that sludge thickening and digesting treatments significantly influenced the total metal concentrations. Fe, Cu, Ni, Cr, Mo, and Pb distributed principally in the residual fraction in all sludges, while Zn and Mn presented in a highly available fraction. For same metal in different sludges, the portion of easily mobile fraction decreased significantly along the wastewater treatment process, and metals in AS presented in the highest available fraction. Organic matter contents, TN, and TP of sludges exhibited a significant positive correlation with the concentrations of exchangeable and reducible fraction of Pb, Mo, Cr, Cu, and Fe, while sludge pH demonstrated significant negative correlations with the concentrations of these metals.     

The influence of heavy metals on the polymorphs of dicalcium silicate in the belite-rich clinkers produced from electroplating sludge

The purpose of this study is to utilize an electroplating sludge for belite-rich clinker production and to observe the influence of heavy metals on the polymorphs of dicalcium silicate (C₂S). Belite-rich clinkers prepared with 0.5–2% of NiO, ZnO, CuO, and Cr₂O₃ were used to investigate the individual effects of the heavy metals in question. The Reference Intensity Ratio (RIR) method was employed to determine the weight fractions of γ-C₂S and β-C₂S in the clinkers, and their microstructures were examined by the transmission electron microscopy (TEM). The results showed that nickel, zinc, and chromium have positive effects on β-C₂S stabilization (Cr³⁺ > Ni²⁺ > Zn²⁺), whereas copper has a negative effect. The addition of up to 10% electroplating sludge did not have any negative influence on the formation of C₂S. It was observed that γ-C₂S decreased while β-C₂S increased with a rise in the addition of the electroplating sludge. Moreover, nickel and chromium mainly contributed to stabilizing β-C₂S in the belite-rich clinkers produced from the electroplating sludge.     

Total concentrations and speciation of heavy metals in municipal sludge from Changsha, Zhuzhou and Xiangtan in middle-south region of China

The presence of heavy metals in municipal sludge restricts its use for agricultural purposes. In this paper, the bioavailability and eco-toxicity of heavy metals in municipal sludge was evaluated, taking into consideration both the speciation of metals and the local environmental characteristics. The dewatered municipal sludge samples were collected from five sewage plants in Changsha, Zhuzhou and Xiangtan respectively, which are representative cities with characteristics of the middle-south region of China. Some agricultural significant parameters and total metal concentrations in the sludge were determined and the metal speciation was studied by using BCR sequential extraction procedure. It was found experimentally that in general the municipal sludge collected from the five sewage plants was rich in organics, N and P. Except that the sludge from Xia Wan Sewage Treatment Plant showed higher concentrations of heavy metals, the sludge from other plants all showed a low total content of heavy metals with only Cd slightly exceeding the permitted values of the national application standard of acid soil in China (GB18918-2002). The sequential extraction results showed that Cu and Zn were principally distributed in the oxidizable fraction, which meant a high potential toxicity, but the bioavailability of Zn might be overestimated to the soil of Hunan. Pb was mainly in the residual fraction. The distribution of Cd showed no obvious characteristics.     

Selective removal of heavy metal ions in aqueous solutions by sulfide-selector intercalated layered double hydroxide adsorbent

Remaining largely under-appreciated, a majority of metal ion sorbents are limited in their target selectivity. In this work, a 3D sulfide intercalated NiFe-layered double hydroxide (NFL-S) hierarchical sorbent has been synthesized for selective heavy metal removal. The intercalation of sulfurated groups in the interlayer of the layered double hydroxide (LDH) nanosheets endows NFL-S as a selective heavy metal ion filter; the selectivity of NFL-S for heavy metals is in the order of Pb²⁺ > Cu²⁺ ≥ Zn²⁺ > Cd²⁺> Mn²⁺, and NFL-S has high k_d values for Pb²⁺ (∼10⁶ mL/g) and Cu²⁺ (∼10⁵ mL/g). Scanning electron microscopy, X-ray photoelectron spectroscopy and powder X-ray diffraction were used to analyze the composition of the as-prepared nanoadsorbent. The selective adsorption behavior was systematically studied using batch experiments, and the performance was evaluated through kinetic and isotherm studies. Moreover, the adsorption mechanism of heavy metals by NFL-S through surface complexation was also investigated, which shows great potential for water decontamination.     

Efficient removal of heavy metal ions from aqueous solution using salicylic acid type chelate adsorbent

In this study, 5-aminosalicylic acid was successfully grafted onto the poly(glycidyl methacrylate) (PGMA) macromolecular chains of PGMA/SiO₂ to obtain a novel adsorbent designated as ASA-PGMA/SiO₂. The adsorption properties of ASA-PGMA/SiO₂ for heavy metal ions were studied through batch and column methods. The experimental results showed that ASA-PGMA/SiO₂ possesses strong chelating adsorption ability for heavy metal ions, and its adsorption capacity for Cu²⁺, Cd²⁺, Zn²⁺, and Pb²⁺ reaches 0.42, 0.40, 0.35, and 0.31 mmol g⁻¹, respectively. In addition, pH has a great influence on the adsorption capacity in the studied pH range. The adsorption isotherm data greatly obey the Langmuir and Freundlich model. The desorption of metal ions from ASA-PGMA/SiO₂ is effective using 0.1 mol l⁻¹ of hydrochloric acid solution as eluent. Consecutive adsorption-desorption experiments showed that ASA-PGMA/SiO₂ could be reused almost without any loss in the adsorption capacity.     

Simultaneous removal of phenol, ammonium and thiocyanate from coke wastewater by aerobic biodegradation

A laboratory-scale activated sludge plant composed of a 20 L volume aerobic reactor followed by a 12 L volume settling tank and operating at 35 degrees C was used to study the biodegradation of coke wastewater. The concentrations of ammonium nitrogen (NH(4)(+) -N), phenols, chemical oxygen demand (COD) and thiocyanate (SCN(-)) in the wastewater ranged between 504 and 2,340, 110 and 350, 807 and 3,275 and 185 and 370 mg/L, respectively. The study was undertaken with and without the addition of bicarbonate. The addition of this inorganic carbon source was necessary to favour nitrification, as the alkalinity of the wastewater was very low. Maximum removal efficiencies of 75%, 98% and 90% were obtained for COD, phenols and thyocianates, respectively, without the addition of bicarbonate. The concentration of ammonia increased in the effluent due to both the formation of NH(4)(+) as a result of SCN(-) biodegradation and to organic nitrogen oxidation. A maximum nitrification efficiency of 71% was achieved when bicarbonate was added, the removals of COD and phenols being almost similar to those obtained in the absence of nitrification. Batch experiments were performed to study the influence of pH and alkalinity on the biodegradation of phenols and thiocyanate.     

Enhancing the use of waste activated sludge as bio-fuel through selectively reducing its heavy metal content

Power plant or cement kiln co-incineration are important disposal routes for the large amounts of waste activated sludge (WAS) which are generated annually. The presence of significant amounts of heavy metals in the sludge however poses serious problems since they are partly emitted with the flue gases (and collected in the flue gas dedusting) and partly incorporated in the ashes of the incinerator: in both cases, the disposal or reuse of the fly ash and bottom ashes can be jeopardized since subsequent leaching in landfill disposal can occur, or their "pozzolanic" incorporation in cement cannot be applied. The present paper studies some physicochemical methods for reducing the heavy metal content of WAS. The used techniques include acid and alkaline thermal hydrolysis and Fenton's peroxidation. By degrading the extracellular polymeric substances, binding sites for a large amount of heavy metals, the latter are released into the sludge water. The behaviour of several heavy metals (Cd, Cr, Cu, Hg, Pb, Ni, Zn) was assessed in laboratory tests. Results of these show a significant reduction of most heavy metals.     

高温堆的热利用--热化学循环制氢的研究

利用高温堆提供的900℃的高温热源，用碘－硫（IS）循环热化学水解的方法可得到没有二氧化碳释放的能源系统。介绍了IS循环的概念、IS循环实验室规模生产氢气的实验验证以及对IS循环闭合回路改进的研究。     

Cyanide removal from cassava mill wastewater using Azotobactor vinelandii TISTR 1094 with mixed microorganisms in activated sludge treatment system

Cassava mill wastewater has a high organic and cyanide content and is an important economic product of traditional and rural low technology agro-industry in many parts of the world. However, the wastewater is toxic and can pose serious threat to the environment and aquatic life in the receiving waters. The ability of Azotobactor vinelandii TISTR 1094, a N₂-fixing bacterium, to grow and remove cyanide in cassava wastewater was evaluated. Results revealed that the cells in the exponential phase reduce the level of cyanide more rapidly than when the cells are at their stationary growth phase. The rate of cyanide removal by A. vinelandii depends on the initial cyanide concentration. As the initial cyanide concentration increased, removal rate increased and cyanide removal of up to 65.3% was achieved. In the subsequent pilot scale trial involving an activated sludge system, the introduction of A. vinelandii into the system resulted in cyanide removals of up to 90%. This represented an improvement of 20% when compared to the activated sludge system which did not incorporate the strain.     

离子膜电解去除味精废水中氨氮的研究

采用离子膜电解法对高浓度氨氮废水进行脱氨预处理,对影响氨氮去除的几种因素进行了研究.6 V、60℃下去除率在75%以上.脱除的氨氮以浓氨水的形式回收,实现废物资源化.废水经脱氨后出水基本无色,COD也有一定降低.综合考虑能耗后,得出本实验条件下适宜的操作条件,去除率平均接近64%,为工业化应用提供了依据.     

Effects of particulates, heavy metals and acid gas on the removals of NO and PAHs by V2O5–WO3 catalysts in waste incineration system

This study investigated the activities of prepared and commercial V₂O₅–WO₃ catalysts for simultaneous removals of NO and polycyclic aromatic hydrocarbons (PAHs) and the influences of particulates, heavy metals, SO₂, and HCl on the performances of catalysts. The experiments were carried out in a laboratory-scale waste incineration system equipped with a catalyst reactor. The DREs of PAHs by prepared and commercial V₂O₅–WO₃ catalysts were 64% and 72%, respectively. Increasing the particulate concentrations in flue gas suppressed the DRE of PAHs, but increasing the carbon content on surface of catalysts promotes the NO conversions. The DRE of PAHs by the catalysts was significantly decreased by the increased concentrations of heavy metal Cd, but was promoted by high concentration of Pb. The influence level of SO₂ was higher than HCl on the performances of V₂O₅–WO₃ catalysts for PAHs removal, but was lower than HCl for NO removal. Prepared and commercial V₂O₅–WO₃ catalysts have similar trends on the effects of particulates, heavy metals, SO₂, and HCl. The results of ESCA analysis reveal that the presences of these pollutants on the surface of catalysts did not change the chemical state of V and W.