Kinetic and mechanism studies of the adsorption of lead onto waste cow bone powder (WCBP) surfaces

This study examines the adsorption isotherms, kinetics and mechanisms of Pb2(+) sorption onto waste cow bone powder (WCBP) surfaces. The concentrations of Pb2(+) in the study range from 10 to 90 mg/L. Although the sorption data follow the Langmuir and Freundlich isotherm, a detailed examination reveals that surface sorption or complexation and co-precipitation are the most important mechanisms, along with possibly ion exchange and solid diffusion also contributing to the overall sorption process. The co-precipitation of Pb2(+) with the calcium hydroxyapatite (Ca-HAP) is implied by significant changes in Ca2(+) and PO?3? concentrations during the metal sorption processes. The Pb2(+) sorption onto the WCBP surface by metal complexation with surface functional groups such as ≡ POH. The major metal surface species are likely to be ≡ POPb(+). The sorption isotherm results indicated that Pb2(+) sorption onto the Langmuir and Freundlich constant q(max) and K( F ) is 9.52 and 8.18 mg g?1, respectively. Sorption kinetics results indicated that Pb2(+) sorption onto WCBP was pseudo-second-order rate constants K? was 1.12 g mg?1 h?1. The main mechanism is adsorption or surface complexation (≡POPb(+): 61.6%), co-precipitation or ion exchange [Ca?(.)?? Pb?(.)?? (PO?)? (OH): 21.4%] and other precipitation [Pb 50 mg L?1 and natural pH: 17%). Sorption isotherms showed that WCBP has a much higher Pb2(+) removal rate in an aqueous solution; the greater capability of WCBP to remove aqueous Pb2(+) indicates its potential as another promising way to remediate Pb2(+)-contaminated media.     

A dual-mesh approach to ring-rolling simulations with emphasis on remeshing

In this paper, we present a ring-rolling simulation technique, with emphasis on remeshing capabilities. The technique is based on a dual-mesh approach, in which a finite element analysis model is divided into fine sectors and coarse sectors, and three different kinds of remeshing are used. The first of these, which is obligatory, replaces a coarse sector with a fine sector when the coarse sector approaches a plastic deformation zone. The second and third kinds, which are introduced in this study, respectively involve changing the number of sectors and changing the grid system of the frames used to construct the sectors. These remeshing schemes are discussed in detail, and several applications are utilized to demonstrate their characteristics and capabilities in the dual-mesh approach to ring-rolling simulations.     

Automatic verification of control logics in safety instrumented system design for chemical process industry

Automatic model checking is used to determine the error-free design of the SIS (Safety Instrumented System) and to find the logical errors in the chemical processes. It proposes an automatic technique to provide and to modify the P&ID design of SIS control logics. This method can be applied to verify its correctness of SIS and to find the logical errors by synthesizing a feasible sequence automatically. This study focuses on automatic verifying and synthesizing for the design, operability and reachability of SIS control logics in chemical processes.     

Mineralization of phenol by Ce(IV)-mediated electrochemical oxidation in methanesulphonic acid medium: a preliminary study

The mediated electrochemical oxidation (MEO) process using cerium(IV) in methanesulphonic acid (MSA) as the oxidizing medium was employed for the mineralization of phenol in batch and continuous feeding modes. Although nitric acid was an extensively studied electrolyte for organic mineralization reactions in MEO processes it does possess the problem of NO(x) gas production during the reduction of nitric acid in the cathode compartment of the electrochemical cell. This problem could be circumvented by proper choice of the electrolyte medium such as MSA. The mediator cerium in MSA solution was first oxidized to higher oxidation state using an electrochemical cell. The produced Ce(IV) oxidant was then used for the destruction of phenol. It was found that phenol could be mineralized to CO2 by Ce(IV) in MSA. The evolved CO2 was continuously measured and used for the calculation of destruction efficiency. The destruction efficiency was observed to be 85% based on CO2 evolution for 1000 ppm phenol solution at 80 degrees C in continuous feed mode.     

Effect of long chain fatty acids removal as a pretreatment on the anaerobic digestion of food waste

This study investigated the effect of long chain fatty acids (LCFAs) removal as a pretreatment prior to anaerobic digestion on the production of methane from food waste. The results showed that the anaerobic digestion of food waste containing 1.6 g COD/L of LCFAs was not inhibited (4 days lag-time, 78.3 % methane recovery in 35 days) compared to that of lipid free food waste (3 days lag time, 72.5 % methane recovery in 35 days); however, some unsaturated LCFAs, which are toxic to microorganism, were accumulated in the batch anaerobic digestion reactor. Meanwhile, in a methanogenic activity study, the activity of methanogens was observed to be linearly inhibited by the presence of more than 1 g COD/L of LCFAs. The possibility of the accumulation of unsaturated LCFAs in the reactor should be considered when operating a large-scale continuous system.     

Physicochemical and mineralogical characterization of soil-saprolite cores from a field research site, Tennessee

Site characterization is an essential initial step in determining the feasibility of remedial alternatives at hazardous waste sites. Physicochemical and mineralogical characterization of U-contaminated soils in deeply weathered saprolite at Area 2 of the DOE Field Research Center (FRC) site, Oak Ridge, TN, was accomplished to examine the feasibility of bioremediation. Concentrations of U in soil-saprolite (up to 291 mg kg(-1) in oxalate-extractable U(o)) were closely related to low pH (ca. 4-5), high effective cation exchange capacity without Ca (64.7-83.2 cmol(c) kg(-1)), amorphous Mn content (up to 9910 mg kg(-1)), and the decreased presence of relative clay mineral contents in the bulk samples (i.e., illite 2.5-12 wt. %, average 32 wt. %). The pH of the fill material ranged from 7.0 to 10.5, whereas the pH of the saprolite ranged from 4.5 to 8. Uranium concentration was highest (about 300 mg kg(-1)) at around 6 m below land surface near the saprolite-fill interface. The pH of ground water at Area 2 tended to be between 6 and 7 with U concentrations of about 0.9 to 1.7 mg L(-1). These site specific characteristics of Area 2, which has lower U and nitrate contamination levels and more neutral ground water pH compared with FRC Areas 1 and 3 (ca. 5.5 and <4, respectively), indicate that with appropriate addition of electron donors and nutrients bioremediation of U by metal reducing microorganisms may be possible.     

Water Quality and Pollution in the Hunchun Basin, China

Chemical properties and pollution of water resources were studied in the Hunchun basin, which is located in northeast China and borders directly North Korea and Russia along the Tumen river. Water quality was characterised according to its major constituents and geological features. Ground waters could generally be grouped into (Ca+Mg)-HCO₃ type and (Ca+Mg)-(SO₃+Cl) type in first and the second terrace areas, respectively. The mixing of these two types depends on the local conditions, such as pumping or permeability variations.Hunchun city is a pollution source for local water resources due to its uncontrolled sewage and urban discharge. In a previous study of the southwestern part of the Hunchun basin, groundwater contamination by Fe, Mn and NO₃-N was reported. In addition, this study identified Cd and F as prevailing contaminants in the water resources. Pollution of water resources by these contaminants appeared to be affected by the application of fertilisers, irrigation practice, variation of aquifer characteristics, solubility of mineral phases, and discharge of domestic sewage. Wide distribution and high levels of Cd and F in surface- and ground waters could pose significant problems if they are utilised as major water supply sources.     

Effect of sulfate on the simultaneous bioreduction of iron and uranium

The biogeochemistry related to iron- and sulfate-reducing conditions influences the fate of contaminants such as petroleum hydrocarbons, trace metals, and radionuclides (i.e., uranium) released into the subsurface. An understanding of these processes is imperative to successfully predict the fate of contaminants during bioremediation scenarios. A series of flow-through sediment column experiments were performed to determine if the commencement of sulfate-reducing conditions would occur while bioavailable Fe(III) was present and to determine how the bioreduction of a contaminant (uranium) was affected by the switch from iron-dominated to sulfate-dominated reducing conditions. The results presented herein demonstrated that, under biostimulation, sulfate reduction can commence even though a significant pool of bioavailable Fe(III) is present. In addition, the rate of U(VI) reduction was not negatively affected by the commencement of sulfate-reducing conditions.