A SOC Design of ORICA-based Highly Effective Real-time Multi-channel EEG System.

Independent component analysis (ICA) has been wildly used to improve EEG based application such as brain computer interface (BCI). However, some well know ICA algorithm, such as Infomax ICA, suffering from the problem of convergence latency and make it hard to be apply on real-time application. This paper proposes a highly efficient chip implementation of multi-channel EEG real-time system based on online recursive independent component analysis algorithm (ORICA). The core size of the chip is 1.5525-mm2 using 28nm CMOS technology. The EEG demonstration board will be implemented with the ORICA chip. The operation frequency and power consumption of the chip are 100 MHz and 17.9 mW respectively. The proposed chip was validated with a real-time circuit integrated system and the average correlation coefficient between simulations results and chip processing results is 0.958.

A SOC Design of ORICA-based Highly Effective Real-time Multi-channel EEG System.

Independent component analysis (ICA) has been wildly used to improve EEG based application such as brain computer interface (BCI). However, some well know ICA algorithm, such as Infomax ICA, suffering from the problem of convergence latency and make it hard to be apply on real-time application. This paper proposes a highly efficient chip implementation of multi-channel EEG real-time system based on online recursive independent component analysis algorithm (ORICA). The core size of the chip is 1.5525-mm2 using 28nm CMOS technology. The EEG demonstration board will be implemented with the ORICA chip. The operation frequency and power consumption of the chip are 100 MHz and 17.9 mW respectively. The proposed chip was validated with a real-time circuit integrated system and the average correlation coefficient between simulations results and chip processing results is 0.958.

Effect of metal coordination on photocurrent response properties of a tetrathiafulvalene organogel film.

Organic low molecular weight gelators with a tetrathiafulvalene (TTF) unit have received considerable attention because the formed gels usually exhibit redox active response and conducting or semiconducting properties. However, to our knowledge, metal coordination systems have not been reported for TTF-derived gels up to date. We have designed and synthesized a series of TTF derivatives with a diamide-diamino moiety that can coordinate to specific metal ions with square coordination geometry. Gelation properties and morphologies of the films prepared by the gelators in different hydrophobic solvents are characterized. The TTF derivative with a dodecyl group shows effective gelation properties, and electrodes with the organogel films are prepared. The effect of the Ni(II) and Cu(II) coordination on the photocurrent response property of the electrodes is examined. The metal square coordination significantly increases the photocurrent response. This gel system is the first metal coordination related TTF-gel-based photoelectric material. The mechanism of the metal coordination-improved photocurrent response property is discussed based on the crystal structural analysis and theoretical calculations.

Role of the coordination center in photocurrent behavior of a tetrathiafulvalene and metal complex dyad.

Small organic molecule-based compounds are considered to be promising materials in photoelectronics and high-performance optoelectronic devices. However, photoelectron conversion research based on functional organic molecule and metal complex dyads is very scarce. We design and prepare a series of compounds containing a tetrathiafulvalene (TTF) moiety substituted with pyridylmethylamide groups of formulas [Ni(acac)2L]·2CH3OH (1), [Cu2I2L2]·THF·2CH3CN (2), and [MnCl2L2]n·2nCH3CH2OH (3) (L = 4,5-bis(3-pyridylmethylamide)-4',5'-bimethylthio-tetrathiafulvalene, acac = acetylacetone) to study the role of the coordination center in photocurrent behavior. Complex 1 is a mononuclear species, and complex 2 is a dimeric species. Complex 3 is a two-dimensional (2-D) coordination polymer. Spectroscopic and electrochemical properties of these complexes indicate that they are electrochemically active materials. The tetrathiafulvalene ligand L is a photoelectron donor in the presence of electron acceptor methylviologen. The effect of metal coordination centers on photocurrent response behavior is examined. The redox-active metal coordination centers should play an important role in improvement of the photocurrent response property. The different morphologies of the electrode films reflect the dimensions in molecular structures of the coordination compounds.

A new type of charge-transfer salts based on tetrathiafulvalene-tetracarboxylate coordination polymers and methyl viologen.

Although charge-transfer compounds based on tetrathiafulvalene (TTF) derivatives have been intensively studied, {[cation](n+)·[TTFs](n-)} ion pair charge-transfer (IPCT) salts have not been reported. The aim of this research is to introduce functional organic cations, such as photoactive methyl viologen (MV(2+)), into the negatively charged TTF-metal coordination framework to obtain this new type of IPCT complex. X-ray structural analysis of the four compounds (MV)2[Li4(L)2(H2O)6] (1), {(MV)(L)[Na2(H2O)8]·4H2O}n (2), {(MV)[Mn(L)(H2O)2]·2H2O}n (3), and {(MV)[Mn(L)(H2O)2]}n (4), reveals that the electron donor (D) TTF moiety and the electron acceptor (A) MV(2+) form a regular mixed-stack arrangement in alternating DADA fashion. The TTF moiety and the MV(2+) cation are essentially parallel stacked to form the column structures. The strong electrostatic interaction is a main force to shorten the distance between the cation and anion planes. Optical diffuse-reflection spectra indicate that charge transfer occurs in these complexes. The ESR and magnetic measurements confirm that there is strong charge-transfer-induced partial electron transfer. Compounds 2, 3, and 4 show an effective and repeatable photocurrent response. The current intensities of 3 and 4 are higher than that of 2, which reflects that the coordination center of the Mn(II) ion has a great effect on the increasing photocurrent response.

Survey on production quality of electrodialysis reversal and reverse osmosis on municipal wastewater desalination.

Water shortage has become an emerging environmental issue. Reclamation of the effluent from municipal wastewater treatment plant (WWTP) is feasible for meeting the growth of water requirement from industries. In this study, the results of a pilot-plant setting in Futian wastewater treatment plant (Taichung, Taiwan) were presented. Two processes, sand filter - ultrafiltration - reverse osmosis (SF-UF-RO) and sand filter - electrodialysis reversal (SF-EDR), were operated in parallel to evaluate their stability and filtrate quality. It has been noticed that EDR could accept inflow with worse quality and thus required less pretreatment compared with RO. During the operation, EDR required more frequent chemical cleaning (every 3 weeks) than RO did (every 3 months). For the filtrate quality, the desalination efficiency of SF-EDR ranged from 75 to 80% in continuous operation mode, while the conductivity ranged from 100 to 120 µS/cm, with turbidity at 0.8 NTU and total organic carbon at 1.3 mg/L. SF-EDR was less efficient in desalinating the multivalent ions than SF-UF-RO was. However for the monovalent ions, the performances of the two processes were similar to each other. Noticeably, total trihalomethanes in SF-EDR filtrate was lower than that of SF-UF-RO, probably because the polarization effects formed on the concentrated side of the EDR membrane were not significant. At the end of this study, cost analysis was also conducted to compare the capital requirement of building a full-scale wastewater reclamation plant using the two processes. The results showed that using SF-EDR may cost less than using SF-UF-RO, if the users were to accept the filtrate quality of SF-EDR.