Role of coagulation in membrane filtration of wastewater for reuse

This study explains the role of coagulation in membrane filtration of wastewater for reuse. For this purpose, a coagulation-ultrafiltration (UF) membrane system was used to treat secondary effluent from a nearby wastewater treatment plant using a rotating biological contactor. The study proceeded with the hypothesis that coagulation could affect membrane filtration through two phenomena: change in particle characteristics and contaminant loading reduction. If fouling reduction were observed at a low alum dosage, coagulation would affect membrane performance by changing particle characteristics because contaminant reduction could not be possible at low dosage. If fouling reduction were observed only at a high alum dosage, the role of coagulation would be contaminant loading reduction. Results showed that both phenomena were important. Coagulation improved the membrane performance by changing particle characteristics at a low alum dosage. The improvement was achieved through both a change in particle characteristics and contaminant loading reduction at a high alum dosage. Particle size among various characteristics was found the most important for membrane fouling. Coagulation increased particle size, which led to a reduction of fouling. The beneficial effect from coagulation was observed at both fouling steps of pore blocking/adsorption and cake formation. Coagulation pretreatment was also beneficial for the improvement of the permeate quality in terms of organic matter.     

A pilot plant study for catalytic decomposition of PCDDs/PCDFs over supported chromium oxide catalysts

Chromium oxide catalysts supported on TiO₂ and Al₂O₃ were examined in a fixed-bed flow reactor system for the removal of PCE (perchloroethylene), a simulant of 2,3,7,8-TCDD (2,3,7,8-tetrachlorodibenzo-p-dioxin), and in a pilot plant employing actual flue gas from a sintering plant for the removal of PCDDs/PCDFs (poly-chlorinated dibenzo-dioxin/poly-chlorinated dibenzo-furan). The 12.5 wt.% chromium oxides supported on TiO₂ and Al₂O₃ revealed excellent stability and performance of PCE removal in the feed gas stream containing water vapor. In a pilot plant study, the catalysts washcoated on the honeycomb reactor revealed 93–95% of PCDDs/PCDFs removal activity over CrO_x/Al₂O₃-HC20 (CrO_x/Al₂O₃ catalyst washcoated on 20 cell-honeycomb), and more than 99% of the decomposition activity over CrO_x/TiO₂-HC20 (CrO_x/TiO₂ catalyst washcoated on 20 cell-honeycomb) at 325 °C and 5000 h⁻¹ of reactor space velocity without the de novo synthesis of PCDDs/PCDFs. In particular, CrO_x/TiO₂-HC20 showed 94% of PCDDs/PCDFs decomposition activity even at 280 °C reaction temperature. The catalyst also exhibited significant NO removal activity. The chromium oxide seems to be a promising catalyst for the removal of PCDDs/PCDFs and NO_x contained in the flue gas.     

Compositional dependence of thermal and elastic properties of Cu-Ti-Zr-Ni bulk metallic glasses

Starting from the quaternary Cu47Ti34Zr11Ni8 alloy, the compositional dependence of thermal and elastic properties of Cu-Ti-Zr-Ni alloys was systematically investigated. Quaternary Cu-Ti-Zr-Ni alloys can be cast directly from the melt into copper molds to form fully amorphous strips or rods with the thickness of 3-6 mm. The evidence of the amorphous nature of the cast rods was provided by X-ray spectra. The measured glass transition temperature (Tg) and crystallization temperature (Tx) were obtained for the alloys using differential scanning calorimetry (DSC) at the heating rate of 20 K/s. In the results, the differences between the glass temperature and the crystallization tempera-ture (△Tx=Tx-Tg) are measured with values ranging up to 33-55 K. The reduced glass transition temperature (Trg), which is the ratio of the glass temperature to the liquidus temperature (T1), is often used as an indication of the glass-forming ability of metallic alloys. For the present Cu-Ti-Zr-Ni alloys, this ratio is typically in the range of 0.5838-0.5959, characteristic of metallic alloys with good glass-forming ability. The elastic constants for several selected alloys were measured using ultrasonic methods. The values of the elastic shear modulus, bulk modulus, and Poisson's ratio were also given.     

Constrained doubly coprime factorization for all stabilizing ℋ∞ controllers

The conventional Youla parameterization (equivalently Q-Parameterization) approach to solve ?_∞ optimal control problems requires solving the well-known matrix dilation optimization as a method for satisfying the ?_∞-norm constraint of the closed-loop transfer matrix. As an alternative, this paper presents a constrained doubly coprime factorization so that the ?_∞-norm constraint of the closed-loop transfer matrix can be satisfied without the need for matrix dilation optimization. For a given ?_∞-norm constraint, a constrained plant is suggested from a state estimator that includes the worst-case disturbance and estimation effects. Then, the constrained doubly coprime factorization is derived from the constrained plant model. All the stabilizing ?_∞ controllers are expressed by using the constrained coprime factors. Finally, an application example is provided to demonstrate the effectiveness of the proposed method.     

Dynamic stability of a cantilevered Timoshenko beam on partial elastic foundations subjected to a follower force

This paper presents the dynamic stability of a cantilevered Timoshenko beam with a concentrated mass, partially attached to elastic foundations, and subjected to a follower force. Governing equations are derived from the extended Hamilton’s principle, and FEM is applied to solve the discretized equation. The influence of some parameters such as the elastic foundation parameter, the positions of partial elastic foundations, shear deformations, the rotary inertia of the beam, and the mass and the rotary inertia of the concentrated mass on the critical flutter load is investigated. Finally, the optimal attachment ratio of partial elastic foundation that maximizes the critical flutter load is presented.     

Composition-Dependent Thermoelectric Properties of n-Type Bi2Te2.7Se0.3 Doped with In4Se3

We present the effects of In₄Se₃ addition on thermoelectric properties of n-type Bi₂Te_2.7Se_0.3. In this study, polycrystalline (In₄Se₃) _x -(Bi₂Te_2.7Se_0.3)_1?x pellets were prepared by mechanical alloying followed by spark plasma sintering (SPS). The thermoelectric properties such as Seebeck coefficient and electrical and thermal conductivities were measured in the temperature range of 300 K to 500 K. Addition of In₄Se₃ into Bi₂Te_2.7Se_0.3 resulted in segregation of In₄Se₃ phase within Bi₂Te_2.7Se_0.3 matrix. The Seebeck coefficient of the (In₄Se₃) _x -(Bi₂Te_2.7Se_0.3)_1?x samples exhibited lower values compared with that of pure Bi₂Te_2.7Se_0.3 phase. This reduction of Seebeck coefficient in n-type (In₄Se₃) _x -(Bi₂Te_2.7Se_0.3)_1?x is attributed to the formation of unwanted p-type phases by interdiffusion through the interface between (In₄Se₃) _x and (Bi₂Te_2.7Se_0.3)_1?x as well as consequently formed Te-deficient matrix. However, the decrease in electrical resistivity and thermal conductivity with addition of In₄Se₃ leads to an enhanced thermoelectric figure of merit (ZT) at a temperature range over 450 K: a maximum ZT of 1.0 is achieved for the n-type (In₄Se₃)_0.03-(Bi₂Te_2.7Se_0.3)_0.97 sample at 500 K.     

Electrochemical stability of bis(trifluoromethanesulfonyl)imide-based ionic liquids at elevated temperature as a solvent for a titanium oxide bronze electrode

Four different electrolytes are prepared by dissolving a Li salt in three different room-temperature ionic liquids (RTILs) and also in a conventional organic solvent. The cathodic (electrochemical reduction) stability of these electrolytes is compared at both ambient and elevated temperature by potential cycling on a TiO₂-B electrode. At room temperature, the stability of pyrrolidinium- and piperidinium-based RTILs is comparable with that of the carbonate-based organic solvent, which is in contrast to the severely decomposed imidazolium-based RTIL. At elevated temperature (120 °C), the imidazolium-based RTIL undergoes even more significant cathodic decomposition that results in the deposition of a resistive surface film and leads to eventual cell degradation. By contrast, the cathodic decomposition and concomitant film deposition are not serious with pyrrolidinium- and piperidinium-based RTILs even at this high-temperature, so that the TiO₂-B/Li cell operates with reasonably good cycle performance. The latter two RTILs appear to be promising solvents for lithium-ion batteries that are durable against occasional exposure to high-temperature.     

Influence of Cu powders on the wettability and mechanical properties of solderable epoxy composites

Journal of Materials Science: Materials in Electronics - A Cu powder-filled solderable epoxy composite (Cu-SEC), in which Cu powders were applied as reinforcement materials, was developed to...     

Robust control of robot manipulator with actuators

A Robust controller is designed for cascaded nonlinear uncertain systems that can be decomposed into two subsystems; that is, a series connection of two nonlinear subsystems, such as a robot manipulator with actuators. For such systems, a recursive design is used to include the second subsystem in the robust control. The recursive design procedure contains two steps. First, a fictitious robust controller for the first subsystem is designed as if the subsystem had an independent control. As the fictitious control, a nonlinearH∞ control using energy dissipation is designed in the sense ofL ₂-gain attenuation from the disturbance caused by system uncertainties to performance vector. Second, the actual robust control is designed recursively by Lyapunov’s second method. The designed robust control is applied to a robotic system with actuators, in which the physical control inputs are not the joint torques, but electrical signals to the actuators.     

Use of Self-assembled Monolayers at Variable Coverage to Control Interface Bonding in a Model Study of Interfacial Fracture: Pure Shear Loading

The relationships between fundamental interfacial interactions, energy dissipation mechanisms, and fracture stress or fracture energy in a glassy thermoset/inorganic solid joint are not well understood. This subject is addressed with a model system involving an epoxy adhesive on a polished silicon wafer containing its native oxide. The proportions of physical and chemical interactions at the interface, and the in-plane distribution, are varied using self-assembling monolayers of octadecyltrichlorosilane (ODTS). The epoxy interacts strongly with the bare silicon oxide surface, but interacts only weakly with the methylated tails of the ODTS monolayer. The fracture stress is examined as a function of ODTS coverage in the napkin-ring (nominally pure shear) loading geometry. The relationship between fracture stress and ODTS coverage is catastrophic, with a large change in fracture stress occurring over a narrow range of ODTS coverage. This transition in fracture stress does not correspond to a wetting transition of the epoxy. Rather, the transition in fracture stress corresponds to the onset of large-scale plastic deformation within the epoxy. We postulate that the transition in fracture stress occurs when the local stress that the interface can support becomes comparable to the yield stress of the epoxy. The fracture results are independent of whether the ODTS deposition occurs by island growth (T _dep = 10°C) or by homogeneous growth (T _dep = 24°C).