沿面放电氧化液相亚硫酸铵

为了解决湿式氨法烟气脱硫生成不稳定亚硫酸铵（（NH4）2SO3）副产物的问题,设计了以不锈钢弹簧和溶液分别作为高压和低压电极的沿面放电系统,对液相（NH4）2SO3的氧化进行了研究。空气从反应器上方进入后经放电区域形成活性物质,再由底部的曝气头鼓入溶液并与（NH4）2SO3发生反应。比较了沿面放电处理与传统曝气处理的氧化效率,考察了放电电压、载气气量和初始浓度等因素对（NH4）2SO3氧化的影响。结果表明,沿面放电对（NH4）2SO3有显著的氧化效果;优化条件下的（NH4）2SO3氧化率接近100%;溶液中（NH4）2SO4与（NH4）2SO3的浓度比小于1时有利于（NH4）2SO3的氧化。     

氢氧化钠-钢渣双碱法烧结烟气脱硫工艺

在鼓泡反应器中考察了氢氧化钠-钢渣双碱法烧结烟气脱硫的主要影响因素。结果表明,在温度为常温,钢渣反应时间为2 h,钢渣加入量为40 g,SO2进口浓度为2 400 mg/m3,钢渣粒径为200目以上,烟气流量为0.05 m3/h,循环液pH保持在7～8,Na+浓度为0.5 mol/L,循环液为500 mL的条件下,脱硫率可长时间保持在80%以上。同时,对钢渣-氢氧化钠双碱法烧结烟气脱硫机理进行了探讨。     

钢渣掺量对泡沫混凝土砌块性能的影响

泡沫混凝土是一种环保、节能的保温隔热材料,以其优良的保温性能,受到越来越多研究者的关注。对钢渣的特性进行了分析测试,对钢渣不同掺量对泡沫混凝土砌块特性的影响进行了研究,结果表明,采用添加5％～35％钢渣所制备的钢渣泡沫混凝土砌块,其密度等级为JC／T1062—2007中的B10级,掺人5％、15％钢渣的泡沫混凝土抗压强度达到A3．5等级,掺人25％、35％钢渣的泡沫混凝土抗压强度达到A2．5等级。随着钢渣掺量的增大,抗压强度、抗折强度降低,吸水率增大。在同一钢渣掺量的情况下,泡沫混凝土砌块的抗压强度变化率增加显著,而且随着钢渣的加入量升高而增大。钢渣的加入有利于提高泡沫混凝土砌块的后期抗压强度。     

Field Measurements of Natural and Fertilizer-Induced N2O Release Rates from Soils

The influence of the soil on atmospheric N₂O was studied by In-situ measurements in 1976–1979 at several field stations near Mainz, Germany, where different soil types were located. Measurements were carried out using the closed chamber method and applying stainless steel capillaries allowing soil air sampling down to 60 cm depth. The N2O In soil was found to be produced and consumed simultaneously In the uppermost soil layer resulting In a net flux of N₂O with release rates of 0.5–16 μg N₂O–Nm^?2h^?1 on unfertilized natural as well as agriculturally used soils. After fertilization with mineral fertilizers the N₂O release rates increased to values ≤43 μg N₂O–Nm^?2h^?1. The total amount of fertilizer-N released Into the atmosphere as N₂O was determined to be 0.01–0.05% for nitrate and 0.03–0.09 % for ammonium fertilizer.     

High-capacity adsorbents from stainless steel slag for the control of dye pollutants in water

Environmental Science and Pollution Research - Adsorbent materials for the control of dye pollutants in water were synthetized from stainless steel slag (SSS) using different acid-base treatments....     

Effects of alkaline and bioorganic amendments on cadmium,lead, zinc,and nutrient accumulation in brown rice and grain yield in acidic paddy fields contaminated with a mixture of heavy metals

Paddy soils and rice (Oryza sativa L.) contaminated by mixed heavy metals have given rise to great concern. Field experiments were conducted over two cultivation seasons to study the effects of steel slag (SS), fly ash (FA), limestone (LS), bioorganic fertilizer (BF), and the combination of SS and BF (SSBF) on rice grain yield, Cd, Pb, and Zn and nutrient accumulation in brown rice, bioavailability of Cd, Pb, and Zn in soil as well as soil properties (pH and catalase), at two acidic paddy fields contaminated with mixed heavy metals (Cd, Pb, and Zn). Compared to the controls, SS, LS, and SSBF at both low and high additions significantly elevated soil pH over both cultivation seasons. The high treatments of SS and SSBF markedly increased grain yields, the accumulation of P and Ca in brown rice and soil catalase activities in the first cultivation season. The most striking result was from SS application (4.0 t ha^?1) that consistently and significantly reduced the soil bioavailability of Cd, Pb, and Zn by 38.5–91.2 % and the concentrations of Cd and Pb in brown rice by 20.9–50.9 % in the two soils over both cultivation seasons. LS addition (4.0 t ha^?1) also markedly reduced the bioavailable Cd, Pb, and Zn in soil and the Cd concentrations in brown rice. BF remobilized soil Cd and Pb leading to more accumulation of these metals in brown rice. The results showed that steel slag was most effective in the remediation of acidic paddy soils contaminated with mixed heavy metals.     

利用钢渣对聚驱采油废水进行深度处理

利用钢渣对模拟聚驱采油废水进行深度处理,依靠吸附作用去除水中的HPAM。考察了钢渣粒径、搅拌速度、pH以及吸附时间对HPAM去除率的影响,进行了吸附等温线和吸附热力学分析,并对钢渣进行了吸附再生实验。当搅拌速度为250r／min,pH为2～10,吸附时间为90rain,钢渣粒径为10-16目、投加量为100g／100mL时,HPAM的去除率可达到84％以上。钢渣对HPAM的吸附符合Langmuir等温式,吸附自由能变和吸附焓的结果都表明,该吸附属于物理吸附。吸附之后的钢渣可以通过600℃焚烧得到再生,再生后仍可保持良好的吸附性能。     

Mitigation effects of silicon rich amendments on heavy metal accumulation in rice (Oryza sativa L.) planted on multi-metal contaminated acidic soil

The mechanisms of stabilization by silicon-rich amendments of cadmium, zinc, copper and lead in a multi-metal contaminated acidic soil and the mitigation of metal accumulation in rice were investigated in this study. The results from a pot experiment indicated that the application of fly ash (20 and 40 g kg⁻¹) and steel slag (3 and 6 g kg⁻¹) increased soil pH from 4.0 to 5.0-6.4, decreased the phytoavailability of heavy metals by at least 60%, and further suppressed metal uptake by rice. Diffusion gradient in thin-film measurement showed the heavy metal diffusion fluxes from soil to solution decreased by greater than 84% after remediation. X-ray diffraction analysis indicated the mobile metals were mainly deposited as their silicates, phosphates and hydroxides in amended treatments. Moreover, it was found metal translocation from stem to leaf was dramatically restrained by adding amendments, which might be due to the increase of silicon concentration and co-precipitation with heavy metals in stem. Finally, a field experiment showed the trace element concentrations in polished rice treated with amendments complied with the food safety standards of China. These results demonstrated fly ash and steel slag could be effective in mitigating heavy metal accumulation in rice grown on multi-metal contaminated acidic soils.     

Molecular size distribution of compost-derived humates as a function of concentration and different counterions

Conformational changes in the structures of humic acids (HA) extracted from compost with varying degrees of maturity were monitored by high performance size exclusion chromatography (HPSEC). The molecular size distribution of HA was compared in solutions containing sodium or ammonium counterions at pH 7 and pH 4.5. These findings indicate that the humates' molecular size depended not only on the nature of the counterions but also on their concentration in the solution. The physicochemical nature of sodium counterions determined smaller molecular sizes than those of the more hydrated ammonium counterions, at low concentrations of humates. Conversely, at higher humate concentrations, the more compact conformation of sodium humates produced larger molecular sizes than those of ammonium humates due to the aggregation of more hydrophobic surfaces in the sodium humates. Composting led to the degradation of labile microbial components with accumulation of hydrophobic constituents. This caused self-association of hydrophobic compounds into humic superstructures of larger molecular size over composting time. At lower pH, changes in conformational stability by the addition of acetic acid to humate solutions were explained by the supramolecular model of humified organic matter.     

Effects of steel slag amendments on accumulation of cadmium and arsenic by rice (Oryza sativa) in a historically contaminated paddy field

Environmental Science and Pollution Research - Paddy soil contamination by cadmium (Cd) and arsenic (As) is a great concern. Field experiments were conducted to study the effects of steel slag (SS,...     

Pesticide adsorption on a calcareous soil modified with sewage sludge and quaternary alkyl-ammonium cationic surfactants

BACKGROUND, AIM AND SCOPE: Pesticides are often found in soil as a result of their application to control pests. They can be transported on soil particles to surface waters or they can lixiviate and reach other environmental compartments. Soil modification with amendments, such as sewage sludge, and with surfactants, h been proposed to reduce pesticide environmental fate. METHODS: The sorption of atrazine, methidathion and diazinon using the batch technique has been studied on non-modified soil and soil modified with sewage sludge and cationic surfactants, as well as the effect of their addition on soil properties such as organic carbon (OC) content and exchange cations. RESULTS AND DISCUSSION: The OC content of the surfactant modified soils was the highest with the surfactant with the longest hydrocarbon chain (hexadecyltrimethyl ammonium bromide, HDTMA). The results of the OC content run in parallel with the increase in pesticide retention. When the sorption was n malized to soil OC content, the retention induced by addition of HDTMA was still the highest, which is an indication that the organic matter derived from the organic cations is a more effective medium to retain dissolved contaminants, than organic matter from native soil. The addition of sewage sludge to the soil did only result in a slight increase of the soil CEC and, hence, moderately affected the ability of the cationic surfactant to retain the pesticides. CONCLUSIONS: The addition of cationic surfactants to soil would possibly reduce the movement to groundwater of atrazine, methidathion and diazinon. In the case of HDTMA, the decrease in sorption at high surfactant loadings was very slow, being that the surfactant was able to retain the pesticides at concentration values which clearly exceeded the monolayer coverage. RECOMMENDATIONS AND PERSPECTIVES: Contamination by pesticides, which are present in the soil due to their direct input in this medium or to spills or illegal tipping, may be hindered from migration to groundwater by application of a cationic surfactant.     

Advantages and risks of using steel slag in preparing composts from raw organic waste

It had been reported that iron and manganese oxides in steel slag enhanced the production of humic acid (HA) from low-molecular-weight compounds, such as phenolic acids, amino acids, and saccharides. In the present study, this function of steel slag was applied to the composting of raw organic wastes (ROWs). The degree of humification of HAs is an important factor in evaluating compost quality. Thus, HAs were extracted from the prepared composts and the humification parameters were determined, in terms of elemental compositions, acidic functional group contents, molecular weights, spectroscopic parameters from UV–vis absorption and ¹³C NMR spectra. The timing for adding steel slag affected the degree of humification of HAs in the composts. The weight average molecular weight of a HA when slag was added initially (29 kDa) was significantly higher than when slag was added after elevating the temperature of the compost pile (17–18 kDa). These results show that ROWs are decomposed to low-molecular-weight compounds after the pile temperature is elevated and the presence of slag enhances the polycondensation of these compounds to produce HAs with a higher degree of humification. Because the slag used in the present study contained several-tens ng g^?1 to several μg g^?1 of toxic elements (B, Cu, Cr, and Zn), leaching tests for these elements from the prepared composts were carried out. Levels for leaching boron from composts prepared by adding slag (0.2–0.4 mg L^?1) were obviously higher than the corresponding levels without slag (0.05 mg L^?1).     

Evaluation of an In Situ,On-Line Purging System for the Cone Penetrometer

Abstract

Materials that will be used to construct an in situ, on-line purging system for the cone penetrometer were evaluated. Transfer efficiencies for volatile organic compounds (VOCs) through stainless steel, nickel, aluminum, and Teflon® tubings were determined using a gas-phase mixture of VOCs containing trichloromethane, tetrachloromethane, 1,1,1- trichloroethane, tetrachloroethene, hexane, benzene, toluene, and 1,2-dimethylbenzene. The water content of the gas stream had an insignificant effect on the quantitative transfer of VOCs through Teflon® tubing but was critical to efficiently transfer the compounds through metal tubing, particularly nickel. Transfer efficiencies for all eight analytes in moist gas streams through stainless steel were greater than 95%. Toluene, tetrachloroethene, and 1,2-dimethylbenzene were transferred with 93%, 81%, and 80% efficiency, respectively, when they were drawn through Teflon® PFA (perfluoroalkoxy) tubing. In general, the retention of the VOCs by Teflon® increases with decreasing aqueous solubility of the analyte. The efficiencies at which VOCs were purged from aqueous standards in Teflon® PFA, Type 304 stainless steel, and glass vessels were similar. Stainless steel was superior to nickel, aluminum, and the Teflon® polymers as a material for an in situ, on-line purging system for the cone penetrometer.     

Dechlorination of trichloroethylene by a steel converter slag amended with Fe(II)

This study aims to assess the feasibility of using slag, byproduct from iron and steel making industries, as a new reactive material for dechlorination reactions and to investigate dechlorination chemistries of the systems containing the slag and Fe(II). Initially, screening experiments were conducted to evaluate various systems containing slags with or without Fe(II). A combination of the steel converter slag and Fe(II) showed a potential to be developed as a reactive material to treat chlorinated organics. Further kinetic studies with the steel converter slag/Fe(II) systems revealed that the dechlorination capacity of the slag/Fe(II) system is comparable to that of zero-valent iron and generally higher than the cement/Fe(II) system. The slag/Fe(II) system can substantially dechlorinate trichloroethylene (TCE) in the neutral pH region, although the dechlorination rate was greatest in the pH region between 12 and 13. TCE reductions in the slag/Fe(II) system were observed to occur through reductive beta-elimination pathways that produce primarily acetylene and no chlorinated intermediates such as vinyl chloride. These results demonstrate that the steel converter slag with Fe(II) has sound characteristics for an alternative reactive medium for subsurface remediation.     

Ageing of chromium(III)-bearing slag and its relation to the atmospheric oxidation of solid chromium(III)-oxide in the presence of calcium oxide

Slag arising in ferrochromium and stainless steel production is known to contain residual levels of trivalent chromium. As the chromium is normally bound in the slag matrix in various silicate or spinel phases, and hence not easily mobilised, utilisation or controlled disposal of such slag is generally considered unproblematic. Experimental test work with a number of slag materials indicates, however, that very gradual oxidation of trivalent to hexavalent chromium does occur when the slag is exposed to atmospheric oxygen, rendering a quantifiable but small portion of chromium in this much more mobile and toxic form. Mechanisms and rates of the oxidation reaction were investigated in a number of long-term studies using both original slag materials and artificial mixes of chromium and calcium oxides. Powders of these materials, some of them rolled into balls, were left to age under different conditions for periods of up to 12 months. In the slag samples, which contained between 1 and 3 wt.% chromium, 1000–10 000 μg Cr(VI) were found per gram of chromium within 6–9 months of exposure to an ambient atmosphere. The rate of the oxidation reaction decreased exponentially, and the reaction could generally be said to have ceased within 12 months. In mixtures of calcium and chromium oxides the oxidation reaction is presumed to occur at the boundaries between chromium oxide and calcium oxide phases through diffusion of oxygen along the grain boundaries and of Cr³⁺ across the boundaries, resulting in the formation of calcium chromate. In the slags, where calcium and chromium oxide can form a solid solution, the oxidation is likely to occur at the exposed surface of grains containing this solution.     

风淬钢渣对高炉渣基微晶玻璃性能的影响

以风淬钢渣和高炉渣为主要原料,采用一次烧结法制备微晶玻璃。结果表明,该方法制备的微晶玻璃主晶相为钙铝黄长石(Ca2Al2SiO7),还有少量的镁黄长石(Ca2MgSi2O7),钢渣最大用量达到50%;随着风淬钢渣含量的增加,样品的最佳烧结温度逐渐增加;烧结温度对样品析晶性能的影响明显大于风淬钢渣含量的影响;样品的抗折强度随风淬钢渣的增加呈现出先增大后减小的趋势;样品的密度随风淬钢渣的增加而逐渐减小;直接用风淬钢渣和高炉渣制备出的微晶玻璃具有良好的抗折强度和耐酸碱性,抗折强度最大可达90 MPa,该方法为综合治理冶金渣污染及其综合利用开辟了新的途径。     

Ceramic tiles with black pigment made from stainless steel plant dust: Physical properties and long-term leaching behavior of heavy metals

Stainless steel plant dust is a hazardous by-product of the stainless steelmaking industry. It contains large amounts of Fe, Cr, and Ni, and can be potentially recycled as a raw material of inorganic black pigment in the ceramic industry to reduce environmental contamination and produce value-added products. In this paper, ceramic tiles prepared with black pigment through recycling of stainless steel plant dust were characterized in terms of physical properties, such as bulk density, water absorption, apparent porosity, and volume shrinkage ratio, as well as the long-term leaching behavior of heavy metals (Cr, Ni, Pb, Cd, and Zn). The results show that good physical properties of ceramic tiles can be obtained with 8% pigments addition, sample preparation pressure of 25 MPa, and sintering at 1200 ºC for 30 min. The major controlling leaching mechanism for Cr and Pb from the ceramic tiles is initial surface wash-off, while the leaching behavior of Cd, Ni, and Zn from the stabilized product is mainly controlled by matrix diffusion. The reutilization process is safe and effective to immobilize the heavy metals in the stainless steel plant dust.

Implications: Stainless steel plant dust is considered as a hazardous material, and it can be potentially recycled for black pigment preparation in the ceramic industry. This paper provides the characteristics of the ceramic tiles with black pigment through recycling stainless steel plant dust, and the long-term leaching behavior and controlling leaching mechanisms of heavy metals from the ceramic tile. The effectiveness of the treatment process is also evaluated.     

钢渣-灰岩人工湿地脱除粪便污水高氮素的实验研究

构建小试系统研究了钢渣-灰岩垂直潜流人工湿地对粪便污水中高浓度氮素的降解效果。同时比较分析了填料填铺方式和表层填料对钢渣-灰岩垂直潜流湿地降解粪便污水氮素效能的影响。结果表明：当原水氨氮在42.72～272.60 mg/L,总氮在107.40～689.35 mg/L内,钢渣-灰岩垂直潜流人工湿地出水氨氮和总氮浓度可分别达到13.57 mg/L和62.83 mg/L;从长期效果来看,大级配差的正反粒径混合填铺的填料结构更有利于钢渣-灰岩人工湿地保持氮素降解效能;表层的基质材料选择要充分考虑渗透性和复氧能力;钢渣不但对氨氮有吸附作用,而且为氨氮的挥发和硝化/反硝化作用创造有利环境;灰岩在钢渣协助下溶出钙离子以利于氨氮的阳离子交换,同时为铁自养反硝化菌和脱硫杆菌的自养反硝化作用提供碳源。     

钢渣预处理含铬废水及其废渣与铬渣的固化

用钢渣对含铬废水进行预处理,探讨了钢渣粒度、用量、废水pH值和添加硫酸亚铁还原剂的影响.结果表明,经硫酸亚铁还原处理后再用钢渣处理比单纯用钢渣处理的效果明显提高,采用钢渣/总铬质量比为40的100目钢渣处理经硫酸亚铁还原后的含铬废水,总铬和Cr6 去除率分别达79%和84%,采用钢渣柱进行的两级淋滤实验进一步表明该方法可作为工业上含铬废水处理的预处理段.处理后的废钢渣同工业铬渣一起进行水泥固化,标准养护20 d后固化体表面Cr6 浸出率、破碎至5 mm粒径以下和酸雨淋溶下的浸出液Cr6 浓度均符合安全标准,可作为普通建材或进行填埋处置.