Chengsong Qing

Effect of aging time and Al substitution on the morphology of aluminous goethite.

Goethite and Al-substituted goethite were synthesized from the reaction between ferric nitrate and/or aluminum nitrate and potassium hydroxide. XRF, XRD, TEM with EDS were used to characterize the chemical composition, phase and lattice parameters, and morphology of the synthesized products. The results show that d(020) decreases from 4.953 to 4.949Å and the b dimension decreases from 9.951Å to 9.906Å when the aging time increases from 6 days to 42 days for 9.09 mol% Al-substituted goethite. A sample with 9.09 mol% Al substitution in Al-substituted goethite was prepared by a rapid co-precipitation method. In the sample, 13.45 mol%, 12.31 mol% and 5.85 mol% Al substitution with a crystal size of 163, 131, and 45 nm are observed as shown in the TEM images and EDS. The crystal size of goethite is positively related to the degree of Al substitution according to the TEM images and EDS results. Thus, this methodology is proved to be effective to distinguish the morphology of goethite and Al substituted goethite.

Confirmation of the assignment of vibrations of goethite: An ATR and IES study of goethite structure

Transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM/EDS) and X-ray diffraction (XRD) were used to characterize the morphology of synthetic goethite. The behavior of the hydroxyl/water molecular units of goethite and its thermally treated products were characterized using Fourier transform-infrared emission spectroscopy (FT-IES) and attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy. The results showed that all the expected vibrational bands between 4000 and 650 cm(-1) including the resolved bands (3800-2200 cm(-1)) were confirmed. A band attributed to a new type of hydroxyl unit was found at 3708 cm(-1) and assigned to the FeO-H stretching vibration without hydrogen bonding. This hydroxyl unit was retained up to the thermal treatment temperature of 500 °C. On the whole, seven kinds of hydroxyl units, involving three surface hydroxyls, a bulk hydroxyl, a FeO-H without hydrogen bonding, a nonstoichiometric hydroxyl and a reversed hydroxyl were observed, and three kinds of adsorbed water were found in/on goethite.

Effect of rehydration on structure and surface properties of thermally treated palygorskite

Palygorskite has a fibrous like morphology with a distinctive layered appearance. The simplified formula of palygorskite (Mg(5)Si(8)O(20)(OH)(2)(OH(2))(4)·nH(2)O) indicates that two different types of water are present. The dehydration and rehydration of palygorskite have been studied using thermogravimetry and H(2)O-temperature programmed desorption. X-ray diffractograms, NH(3) adsorption profiles, and NH(3) desorption profiles were obtained for thermally treated palygorskite as a function of temperature. The results proved water molecules were mainly derived from Si-OH units. In addition, five kinds of acid sites were found for palygorskite. The number of acid sites of external surfaces was larger than that of the internal surfaces. Bonding on the internal surface acid sites was stronger than the bonding of the external surfaces. Rehydration restored the folded structure of palygorskite when thermal treatment temperature was lower than 300 °C.

Development and application of Palygorskite porous ceramsite in a biological aerated filter (BAF)

Novel filter Palygorskite porous ceramsite (PC) was prepared using Palygorskite clay, poreforming material sawdust, and sodium silicate with a mass ratio of 10:2:1 after sintering at 700°C for 180 min. PC was characterized with X-ray diffraction, X-ray fluorescence, scanning electron microscopy, elemental, and porosimetry. PC had a total porosity of 67% and specific surface area of 61 m2/g. In order to assess the usefulness of PC as a medium for biological aerated filters (BAF), PC and (commercially available ceramsite) CAC were used to treat wastewater city in two laboratory-scale upflow BAFs. The results showed that the reactor containing PC was more efficient than the reactor containing CAC in terms of total organic carbon (TOC), ammonia nitrogen (NH3-N), and the removal of total nitrogen (TN) and phosphorus (P). This system was found to be more efficient at water temperatures ranging from 20 to 26°C, an air–water (A/W) ratio of 3:1, dissolved oxygen concentration >4.00 mg/L, and hydraulic retention time (HRT) ranging from 0.5 to 7 h. The interconnected porous structure produced for PC was suitable for microbial growth, and primarily protozoan and metazoan organisms were found in the biofilm. Microorganism growth also showed that, under the same submerged culture conditions, the biological mass in PC was significantly higher than in CAC (34.1 and 2.2 mg TN/g, respectively). In this way, PC media can be considered suitable for the use as a medium in novel biological aerated filters for the simultaneous removal of nitrogen and phosphorus.

Simultaneous removal of nitrogen and phosphorus using autoclaved aerated concrete particles in biological aerated filters

AbstractAutoclaved aerated concrete particles (AACPs) were developed as alternative for the biofilter carriers. To obtain high biomass concentration, the biogenic stimulating properties of the AACPs were investigated. Meanwhile, the feasibility of using these particles as biological aerated filter media was assessed. The experimental results showed that the removal efficiencies of chemical oxygen demand (CODCr) and total nitrogen (TN) both increased with the increase in the ratio of CODCr to -N (C/N) in the biofilters. It could be demonstrated that the well-developed porous structures of AACPs were conducive to many microbial communities, resulting in an improvement of the permeability of biofilm layers and the pollutant removal efficiencies. The adoption of AACPs in such an environment significantly improved phosphate removal from wastewater. Our findings suggested that AACPs can play significant roles as carriers in simultaneous nitrification and denitrification by biological wastewater treatment systems.

Goethite promoted biodegradation of 2,4-dinitrophenol under nitrate reduction condition

Iron oxide may interact with other pollutants in the aquatic environments and further influence their toxicity, transport and fate. The current study was conducted to investigate the biodegradation of 2,4-dinitrophenol (2,4-DNP) in the presence of iron oxide of goethite under anoxic condition using nitrate as the electron acceptor. Experiment results showed that the degradation rate of 2,4-DNP was improved by goethite. High performance liquid chromatography-mass spectra analysis results showed that goethite promoted degradation and transformation of 2,4-diaminophenol and 2-amino-4-nitrophenol (2-nitro-4-aminophenol). Microbial community analysis results showed that the abundance of Actinobacteria, which have the potential ability to degrade PAHs, was increased when goethite was available. This might partially explain the higher degradation of 2,4-DNP. Furthermore, another bacterium of Desulfotomaculum reducens which could reduce soluble Fe(III) and nitrate was also increased. Results further confirmed that nanomaterials in the aquatic environment will influence the microbial community and further change the transformation process of toxic pollutants.

Simultaneous removal of nitrate and phosphate from wastewater by siderite based autotrophic denitrification

The potential of simultaneous removal of nitrate and phosphate from wastewater by a single anaerobic Fe(II) oxidizing denitrifiers (the strain PXL1) was assessed using siderite biofilters under different influent TOC concentrations and hydraulic retention times (HRTs) over a 160-day trial. Higher TOC concentrations promoted NO3- removal, while there was no significant influence on PO43- removal. Lowering down HRT from 10 h to 5 h did not significantly influence NO3- and PO43- removal. The NO3- removal performance and microbial community structure in the biofilters indicated that NO3- was reduced to N2 by both strain PXL1 and heterotrophic Acidovorax delafieldii. Iron content analysis of the used siderite along the biofilters showed that PO43- removal was improved by the bio-oxidation of Fe(II) in siderite to Fe(III) via the strain PXL1. The coexistence of the strain PXL1 and natural siderite in nitrate-contaminated aquifers provides a practical technology for in situ remediation of nutrient contaminated waterbodies.