Revegetation of serpentine substrates: Response to phosphate application

Revegetation was studied on stockpiled serpentine substrate. The native vegetation surrounding the revegetation site is annual grassland. The seed mixture applied to both subsoil and topsoil plots was largely ineffective for revegetation. No growth occurred in the subsoil plots and most of the growth in the topsoil plots was from indigenous seed. Phosphate application (100 kg P ha^–1 as NaH₂PO₄ · H₂O) to the topsoil plots resulted in a significant increase in total above-ground productivity. Annual legumes (mostlyLotus subpinnatus Lag.) and, to a lesser degree,Plantago erecta Morris responded to the added phosphate with an increased above-ground productivity. Other annual forbs and annual grasses showed no significant response. The legumes also increased in abundance. Mycorrhizal root colonization forPlantago was not significantly affected by phosphate application, but was lower in this disturbed serpentine site compared to other undisturbed serpentine annual grassland sites nearby.     

成都施用磷肥中镭（^226Ra）含量调查及对农田环境影响评价

本文报道了成都磷肥及其原料矿石中外照射剂量水平；用国家标准规定的方法测定了磷肥及其矿石中＾２２６Ｒａ含量；调查了同一生产厂家不同批号磷肥中＾２２６Ｒａ含量变化情况；估算出施用磷肥后可能带来的放射性环境污染，并对磷肥中＾２２６Ｒａ可能导致的农田环境影响作了简要评价? ?     

SBR短程脱氮系统中亚硝酸盐积累对生物除磷的影响

采用SBR工艺处理实际生活污水,通过控制好氧段的DO浓度及曝气时间,实现了短程硝化反硝化,并考察了短程硝化引起的亚硝酸盐积累对生物除磷系统的影响.结果表明,在没有补充外碳源的情况下,好氧阶段NO2--N的积累低于10 mg·L-1时,聚磷菌的吸磷及放磷能力没有受到影响,好氧出水磷浓度基本维持在1 mg·L-1以下;当N...     

Phosphate removal from domestic wastewater using thermally modified steel slag

This study was performed to investigate the removal of phosphate from domestic wastewater using a modified steel slag as the adsorbent. The adsorption effects of alkalinity, salt, water,and thermal modification were investigated. The results showed that thermal activation at 800℃ for 1 hr was the optimum operation to improve the adsorption capacity. The adsorption process of the thermally modified slag was well described by the Elovich kinetic model and the Langmuir isotherm model. The maximum adsorption capacity calculated from the Langmuir model reached 13.62 mg/g. Scanning electron microscopy indicated that the surface of the modified slag was cracked and that the texture became loose after heating. The surface area and pore volume did not change after thermal modification. In the treatment of domestic wastewater, the modified slag bed(35.5 kg) removed phosphate effectively and operated for 158 days until the effluent P rose above the limit concentration of 0.5 mg/L. The phosphate fractionation method, which is often applied in soil research, was used to analyze the phosphate adsorption behavior in the slag bed. The analysis revealed that the total contents of various Ca–P forms accounted for 81.4%–91.1%, i.e., Ca10–P 50.6%–65.1%, Ca8–P 17.8%–25.0%,and Ca2–P 4.66%–9.20%. The forms of Al–P, Fe–P, and O–P accounted for only 8.9%–18.6%. The formation of Ca10–P precipitates was considered to be the main mechanism of phosphate removal in the thermally modified slag bed.     

Phosphate removal using aerobic bacterial consortium and pure cultures isolated from activated sludge

In the present study, an attempt is made to evaluate the kinetics of biological phosphate removal using a bacterial consortium of activated sludge, as well as screening for dominant polyphosphates accumulating bacteria. The results showed an efficient phosphate uptake (P < 0.001) of the consortium, with rates related to the initial concentration of both phosphate and carbon sources. Short chain volatile fatty acids presented the suitable substrates for enhanced biological phosphorus removal, of which maximum yield reached 99.23% and 78.51% in basal salt medium supplemented with 0.5% of sodium acetate and lactate respectively. Fifteen phosphate-accumulating bacteria were isolated from the activated sludge and only four isolates were selected and characterized as Pseudomonas aeruginosa AS1, Moraxella lacunata AS2, Acinetobater junii AS3 and Alcaligenes denitrificans AS4. The highest efficiency of phosphate uptake using pure culture was achieved with Ac. junii AS3 (83.36) followed by P. aeruginosa AS1 (81.78%), Al. denitrificans AS4 (76.72%), and M. lacunata AS2 with 50.6%.     

Release of phosphorous from igneous phosphate rock through bioturbation: a low-cost approach for phosphorous fertilization in fish farms

The influence of bioturbation caused by common carp fry was treated in 24 transparent polythene jars (5?L each) in the laboratory and in outdoor vats (150?L), increasing the fertilizer value of phosphate rock in eight treatment combinations in triplicate. Input of water soluble reactive phosphate (SRP) was determined to quantify the effects of bioturbation, fish excrements and soil. The level of SRP in water was always lowest in the control series. Introduction of common carp fry resulted in a net increase of 0.009–0.010?mg phosphate g^?1day^?1 of SRP attributable to the effect of fish excrement. Bioturbation caused by common carp resulted in as high as a 64.8 to 90% influx of phosphate from bottom soil in the presence of phosphate rock but only about 6.3 to 7.2% in the absence of phosphate rock. The bioturbation that occurred in this treatment resulted in a significant release of phosphorous into the overlying water from an apatite source. The results confirm the environment friendly application of phosphate rock in fish-farming ponds at low cost.     

凹凸棒石粘土吸附剂去除磷酸盐的研究

以天然凹凸棒石粘土为吸附剂,采用恒温振荡间歇式吸附处理方法,讨论磷酸盐去除特性。通过对粘土的热处理和表面处理,优化出加工凹凸棒石粘土为除磷吸附剂的适宜处理条件。即通过3 mol/L碱处理12h,并在300℃下灼烧2h可获得对磷酸盐的最佳处理效果。该吸附剂除磷的动力学和热力学性能可分别用扩散控制模式和稳定状态固定反应吸附等温式得到较好的描述,求得单分子层最大吸附量为8.62mg/g。      

Rapid and long-effective removal of broad-spectrum pollutants from aqueous system by ZVI/oxidants

• The coupling of oxidants with ZVI overcome the impedance of ZVI passive layer. • ZVI/oxidants system achieved fast and long-effective removal of contaminants. • Multiple mechanisms are involved in contaminants removal by ZVI/oxidant system. • ZVI/Oxidants did not change the reducing property of ORP in the fixed-bed system. Zero-valent iron (ZVI) technology has recently gained significant interest in the efficient sequestration of a wide variety of contaminants. However, surface passivation of ZVI because of its intrinsic passive layer would lead to the inferior reactivity of ZVI and its lower efficacy in contaminant removal. Therefore, to activate the ZVI surface cheaply, continuously, and efficiently is an important challenge that ZVI technology must overcome before its wide-scale application. To date, several physical and chemical approaches have been extensively applied to increase the reactivity of the ZVI surface toward the elimination of broad-spectrum pollutants. Nevertheless, these techniques have several limitations such as low efficacy, narrow working pH, eco-toxicity, and high installation cost. The objective of this mini-review paper is to identify the critical role of oxygen in determining the reactivity of ZVI toward contaminant removal. Subsequently, the effect of three typical oxidants (H₂O₂, KMnO₄, and NaClO) on broad-spectrum contaminants removal by ZVI has been documented and discussed. The reaction mechanism and sequestration efficacies of the ZVI/oxidant system were evaluated and reviewed. The technical basis of the ZVI/oxidant approach is based on the half-reaction of the cathodic reduction of the oxidants. The oxidants commonly used in the water treatment industry, i.e., NaClO, O₃, and H₂O₂, can be served as an ideal coupling electron receptor. With the combination of these oxidants, the surface corrosion of ZVI can be continuously driven. The ZVI/oxidants technology has been compared with other conventional technologies and conclusions have been drawn.     

Synthesis of vinasse-dolomite nanocomposite biochar via a novel developed functionalization method to recover phosphate as a potential fertilizer substitute

• Nanocomposites were prepared by adding dolomite to vinasse at different ratio. • Textural and morphological features of adsorbents were studied in detail. • CCD based RSM was used for investigation of P ion removal by nanocomposite. • The q_m based on Langmuir model for modified vinasse biochar was 178.57 mg/g. • P loaded nanocomposite improved plant growth and could be utilized as P-fertilizer. The effectiveness of phosphate (P) removal from aqueous solutions was investigated by novel low-cost biochars synthesized from vinasse and functionalized with calcined dolomite. The vinasse-derived biochar, synthesized via pyrolysis at different temperatures, showed easy preparation and a large surface area. The novel vinasse biochar nanocomposites were prepared by adding dolomite to the vinasse biochars with different weight percentages (10, 20 and 30%). The characteristics of the prepared materials were identified for further understanding of the inherent adsorption mechanism between P ions and vinasse biochars. Vinasse-dolomite nanocomposite was very effective in the adsorption of P species from aqueous media. The effect of the operational factors on Vinasse-dolomite nanocomposite was explored by applying response surface methodology (RSM). According to RSM results, the optimum condition was achieved to be contact time 90 (min), 250 (mg/L) of P concentration and pH 7. Thermodynamic isotherm and kinetic studies were applied on experimental data to understand the adsorption behavior. The Vinasse-dolomite nanocomposite revealed preferential P species adsorption in the presence of co-existing anions. The P species could be recovered by 1.0 M HCl where the efficiency was not affected up to the fifth cycle. The P-loaded Vinasse-dolomite nanocomposite was successfully tested on a plant; it significantly improved its growth and proved its potency as a P-based fertilizer substitute.     

Sorption, desorption, and degradation of (4-chloro-2-methylphenoxy)acetic acid in representative soils of the Danubian Lowland, Slovakia

Herbicide leaching through soil into groundwater greatly depends upon sorption-desorption and degradation phenomena. Batch adsorption, desorption and degradation experiments were performed with acidic herbicide MCPA and three soil types collected from their respective soil horizons. MCPA was found to be weakly sorbed by the soils with Freundlich coefficient values ranging from 0.37 to 1.03 mg^1−1/n kg⁻¹ L^1/n. It was shown that MCPA sorption positively correlated with soil organic carbon content, humic and fulvic acid carbon contents, and negatively with soil pH. The importance of soil organic matter in MCPA sorption by soils was also confirmed by performing sorption experiments after soil organic matter removal. MCPA sorption in these treated soils decreased by 37-100% compared to the original soils. A relatively large part of the sorbed MCPA was released from soils into aqueous solution after four successive desorption steps, although some hysteresis occurred during desorption of MCPA from all soils. Both sorption and desorption were depth-dependent, the A soil horizons exhibited higher retention capacity of the herbicide than B or C soil horizons. Generally, MCPA sorption decreased in the presence of phosphate and low molecular weight organic acids. Degradation of MCPA was faster in the A soil horizons than the corresponding B or C soil horizons with half-life values ranging from 4.9 to 9.6 d in topsoils and from 11.6 to 23.4 d in subsoils.