浅谈地下水净化厂除铁除锰试验及应用

通过对齐齐哈尔市自来水公司铁锋水厂除铁、锰工艺的分析,得出曝气接触氧化除铁、锰是一种好方法.     

催化铁应用于草甘膦废水处理工艺改造的可行性研究

针对某化工厂草甘膦废水经厌氧-好氧生物处理后出水总磷浓度高,无法达到该化工区污水纳管标准的情况,应用催化铁方法对该废水现有处理工艺进行改造以提高出水水质。考察了催化铁方法对原处理工艺不同处理工段出水中磷的去除效果,发现该法可有效地去除生物厌氧池出水的总磷及正磷盐,去除率分别达到52．7％和83．13％以上,且使废水的BOD5／COD值显著提高,可从0．08提高至0．31,增强了废水的可生物降解性,有利于后续好氧生物处理的进行。研究表明在原处理工艺的厌氧池后增加催化铁处理段能明显提高最终出水水质。     

韶钢外委项目安全管理措施

随着企业用工制度的改革和深化,多层次、多方位、多形式的用工体系已经形成,给企业固有的安全管理网络体系形成了较大的冲击,特别是《安全生产法》的全面实施,给企业的安全管理工作赋予了更多的内容。针对韶钢外委项日实际情况,论述了外委项目安全管理的措施。     

Potential ZnS fossilization of gastropods (Middle Jurassic claystones from Central Poland)

The rich fossil fauna in the Middle Jurassic claystones that crop out in the Krakow-Czestochowa Upland is extensively replaced by sulfide minerals, mainly pyrite. Sphalerite (ZnS) is rare and restricted to the internal casts of gastropods, often together with framboidal and euhedral pyrite and calcite. Scanning electron microscopy-energy dispersive spectrometer study was undertaken to explain this curious association. The results show that although direct infilling of the carbonate shell, similar to processes occurring during pyritization, is probable, it does not explain all textures observed. We propose that the carbonate shells were initially infilled by calcite and iron sulfides and sphalerite subsequently replaced the calcite casts. Preferential occurrence of ZnS in gastropods could result from accumulation of higher concentration of zinc during the organisms' life. After death, this Zn was introduced into the carbonate making gastropods more prone to ZnS replacement. Formation of ZnS casts was probably a late diagenetic event as zinc content of the surrounding sediment does not appear to influence sphalerite formation.     

Studies on solvent extraction of iron(III) as a step for conversion of a waste effluent to a value added product

Solvent extraction of iron(III) from actual sulphate waste pickle liquor was investigated using trialkylphosphine oxide diluted with kerosene. The waste pickle liquor was procured from a local company which deals with the manufacturing of pipes and tubes made of iron and steel. Various parameters were studied to optimise a suitable condition for the maximum extraction of iron. The composition of the aqueous feed used in the experiment was 60.88 g/L Fe(III), 53 g/L acid with traces of Cu, Ni and Co. An ambient extraction at 30 °C yielded acceptable kinetics and loading efficiency for 40% trialkylphosphine oxide with a saturated loading capacity of 51.85 g/L in four contacts at O/A ratio of 1/1 in a multiple contact mode. Iron from the loaded organic was stripped using various strippants such as distilled water, H₂SO₄ and oxalic acid. Since only 32% of loaded Fe could be stripped with 2 M H₂SO₄ in five contacts, further stripping was done with 5% oxalic acid which showed a very promising result. It was found that almost 100% of Fe(III) could be stripped out with 5% oxalic acid at O/A of 1/1 in five contacts.     

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.     

Preparation and characterization of boron-doped corn straw biochar: Fe (Ⅱ) removal equilibrium and kinetics

Nowadays, iron ions as a ubiquitous heavy metal pollutant are gradually concerned and the convenient and quick removal of excessive iron ions in groundwater has become a major challenge for the safety of drinking water. In this study, boron-doped biochar (B-BC) was successfully prepared at various preparation conditions with the addition of boric acid. The as-prepared material has a more developed pore structure and a larger specific surface area (up to 897.97 m²/g). A series of characterization results shows that boric acid effectively activates biochar, and boron atoms are successfully doped on biochar. Compared with the ratio of raw materials, the pyrolysis temperature has a greater influence on the amount of boron doping. Based on Langmuir model, the maximum adsorption capacity of 800B-BC_1:2 at 25 °C, 40 °C, 55 °C are 50.02 mg/g, 95.09 mg/g, 132.78 mg/g, respectively. Pseudo-second-order kinetic model can better describe the adsorption process, the adsorption process is mainly chemical adsorption. Chemical complexation, ions exchange, and co-precipitation may be the main mechanisms for Fe²⁺ removal.     

Uranium and other trace elements’ distribution in Korean granite: implications for the influence of iron oxides on uranium migration

To understand trace radionuclide (uranium) migration occurring in rocks, a granitic batholith located at the Korea Atomic Energy Research Institute (KAERI) site was selected and investigated. The rock samples obtained from this site were examined using mineralogical methods, including scanning electron microscopy (SEM) and electron probe microanalysis (EPMA). The changes in the distribution pattern of uranium (U) and small amounts of trace elements, and the mineralogical textures affected by weathering, were examined. Based on the element distribution analyses, it was found that Fe²⁺ released from fresh biotite is oxidized in short geological time, forming amorphous iron oxides, such as ferrihydrite, around silicate minerals. In that case, the amorphous ferrihydrite does not show distinct adsorption for U. However, as it gradually crystallizes to goethite or hematite, the most U-rich phases were found to be associated with the secondary iron oxides having granular forms. This evidence suggests that the geological subsurface environment is favorable for the crystallized iron oxides to keep their structures more stable for a long time as compared with the amorphous phases. There is a possibility that the long residence of U which is in contact with the stable crystalline phases of iron may finally lead to the partial sequestration of U in their structure. Consequently, it seems that Fe-oxide crystallization can be a dominating mechanism for U uptake and controls long-term U transport in granites with low U contents.     

铁屑吸附-微波辐照-内电解协同处理结晶紫染料废水

以结晶紫为模型化合物,提出了一种新的“铁屑吸附—微波辐照—内电解”协同处理染料废水的方法。试验结果表明,吸附在铁屑表面的染料通过微波催化裂解和内电解协同作用迅速降解,染料溶液的脱色率和COD去除率分别达到99％和95％以上。废铁屑经8次使用后仍有良好的处理效果。研究了各种相关因素对染料废水脱色的影响。     

Influence of tidal regime on the distribution of trace metals in a contaminated tidal freshwater marsh soil colonized with common reed (Phragmites australis)

A historical input of trace metals into tidal marshes fringing the river Scheldt may be a cause for concern. Nevertheless, the specific physicochemical form, rather than the total concentration, determines the ecotoxicological risk of metals in the soil. In this study the effect of tidal regime on the distribution of trace metals in different compartments of the soil was investigated. As, Cd, Cu and Zn concentrations in sediment, pore water and in roots were determined along a depth profile. Total sediment metal concentrations were similar at different sites, reflecting pollution history. Pore water metal concentrations were generally higher under less flooded conditions (mean is (2.32 ± 0.08) × 10⁻³ mg Cd L⁻¹ and (1.53 ± 0.03) × 10⁻³ mg Cd L⁻¹). Metal concentrations associated with roots (mean is 202.47 ± 2.83 mg Cd kg⁻¹ and 69.39 ± 0.99 mg Cd kg⁻¹) were up to 10 times higher than sediment (mean is 20.48 ± 0.19 mg Cd kg⁻¹ and 20.42 ± 0.21 mg Cd kg⁻¹) metal concentrations and higher under dryer conditions. Despite high metal concentrations associated with roots, the major part of the metals in the marsh soil is still associated with the sediment as the overall biomass of roots is small compared to the sediment.