Neurofuzzy control of a low‐temperature desulphurization plant

Low‐temperature desulphurization (LTD) is a low‐cost alternative to conventional wet scrubbing for removing sulphur dioxide from flue gas produced by power generating plants. A problem in the design of conventional controllers to achieve and maintain process conditions for optimal desulphurisation is the lack of mathematical models to characterise the complex desulphurization process and unexpected environ mental disturbances. The aim of the work reported in this paper was to replace a skilled human operator who could successfully regulate the LTD plant through manipulation of low‐level controllers with a competitive neurofuzzy system, which possesses both the learning ability of neural networks and the structural transparency of fuzzy logic systems. A hierarchical control structure was adopted whereby the competitive neurofuzzy method was used at the top level for co‐ordinating actions of low‐level conventional controllers. This approach would considerably simplify the task of designing the control system and has been shown to yield high‐level controllers with performances at least equalling that of expert operators, as demonstrated in this paper. Copyright © 2001 John Wiley & Sons, Ltd.     

Enhanced removal of 1,2-dichloroethane by anodophilic microbial consortia

1,2-Dichloroethane (1,2-DCA) is a well-known recalcitrant groundwater contaminant. New environment-friendly approaches for the removal of 1,2-DCA that does not bring about volatilization of the compound are required. In this study, different anodophilic consortia enriched in microbial fuel cells (MFCs) operated under airtight conditions were shown to effectively degrade 1,2-DCA (up to 102 mg per liter reactor volume per day), while concomitantly generating a current. An anodophilic consortium previously enriched with acetate as the electron donor changed its composition at the rate of 48% per week and increased its richness (Rr) 3-fold, upon adapting to 1,2-DCA as the new electron donor. After being stable, during 1 month of operation, it removed up to 95% of the 1,2-DCA amount in the medium in the first 2 weeks, while converting 43 ± 4% of electrons available from the removal to electricity. A natural consortium from a 1,2-DCA contaminated site changed its composition at the rate of 9% per week and increased its Rr 2-fold, upon adapting to the MFC anode conditions with 1,2-DCA as the electron donor. After being stable, during 1 month of operation, it removed up to 85% of the 1,2-DCA amount in the medium in the first 2 weeks and the coulombic efficiency was 25 ± 4%. The operation of the MFCs under closed circuit conditions resulted in higher 1,2-DCA removal rates than the operation under open circuit conditions, indicating that bioelectrochemical activities enhanced the removal of 1,2-DCA in the MFC anode. The production of ethylene glycol, acetate and carbon dioxide indicated that the anodophilic bacteria oxidatively metabolized 1,2-DCA, probably by means of a hydrolysis-based pathway. The results show that MFCs can be potentially used as a practically convenient technology for the biological removal of 1,2-DCA.     

Subunit‐Specific Labeling of Ubiquitin Chains by Using Sortase: Insights into the Selectivity of Deubiquitinases

Information embedded in different ubiquitin chains is transduced by proteins with ubiquitin‐binding domains (UBDs) and erased by a set of hydrolytic enzymes referred to as deubiquitinases (DUBs). Understanding the selectivity of UBDs and DUBs is necessary for decoding the functions of different ubiquitin chains. Critical to these efforts is the access to chemically defined ubiquitin chains bearing site‐specific fluorescent labels. One approach toward constructing such molecules involves peptide ligation by sortase (SrtA), a bacterial transpeptidase responsible for covalently attaching cell surface proteins to the cell wall. Here, we demonstrate the utility of SrtA in modifying individual subunits of ubiquitin chains. Using ubiquitin derivatives in which an N‐terminal glycine is unveiled after protease‐mediated digestion, we synthesized ubiquitin dimers, trimers, and tetramers with different isopeptide linkages. SrtA was then used in combination with fluorescent depsipeptide substrates to effect the modification of each subunit in a chain. By constructing branched ubiquitin chains with individual subunits tagged with a fluorophore, we provide evidence that the ubiquitin‐specific protease USP15 prefers ubiquitin trimers but has little preference for a particular isopeptide linkage. Our results emphasize the importance of subunit‐specific labeling of ubiquitin chains when studying how DUBs process these chains.     

A novel hybrid model of Bagging-based Naïve Bayes Trees for landslide susceptibility assessment

Bulletin of Engineering Geology and the Environment - Landslide susceptibility assessment was performed using the novel hybrid model Bagging-based Naïve Bayes Trees (BAGNBT) at Mu Cang Chai...     

Highly sensitive electrochemical sensor based on zirconium oxide-decorated gold nanoflakes nanocomposite 2,4-dichlorophenol detection

Journal of Applied Electrochemistry - In this study, a sensitive and selective electrochemical sensor based on a zirconia oxide-decorated gold nanoflake nanocomposite-modified glassy carbon...     

Chromium(III) compounds as catalysts for Hydrocarbon Oxidation and hydroperoxide decomposition

Chromium stearate and chromium acetylacetonate are very active catalysts both for the oxidation of hydrocarbons by molecular oxygen and for the decomposition of organic hydroperoxides. During these reactions they also catalyze the oxidation of secondary alcohols to the corresponding ketones by organic hydroperoxides. From organic hydroperoxides and chromium(III)compounds chromium (VI) compounds are formed which are probably the effective agents oxidizing secondary alcohols to ketones.     

One-pot synthesis of soluble wholly aromatic liquid crystalline copoly(ester amide)s with high thermal and dimensional stability

Abstract

Thermotropic liquid crystalline polymers (LCPs) have been of great interest for electronic packaging. Herein, we introduce a series of wholly aromatic, thermotropic LCPs from copoly(ester amide)s of 6-hydroxy-2-naphthalic acid, isophthalic acid, terephthalic acid, and 4-aminophenol, prepared by a convenient one-pot melt polycondensation. Almost synthesized copoly(ester amide)s exhibited good solubility in common organic solvents at room temperature. Furthermore, they possessed high thermal stability with 2% degradation temperatures (T_id) of 359–368?°C and the char yields (at 600?°C) of 50.3–55.6%. The synthesized copoly(ester amide)s had relatively low coefficient of thermal expansion (CTE) values, which were 35.85–41.21?ppm °C^?1 in the temperature range of 50–200?°C. Furthermore, an annealing process could be employed to improve the thermomechanical properties of synthesized polymers. For instance, the CTE of sample LCP3 in range temperature of 275–315?°C was reduced by more than 90% after annealing at 320?°C for 1?h, implying the feasibility for electronic packaging.     

Hidden Relationships between N-Glycosylation and Disulfide Bonds in Individual Proteins

N-Glycosylation (NG) and disulfide bonds (DBs) are two prevalent co/post-translational modifications (PTMs) that are often conserved and coexist in membrane and secreted proteins involved in a large number of diseases. Both in the past and in recent times, the enzymes and chaperones regulating these PTMs have been constantly discovered to directly interact with each other or colocalize in the ER. However, beyond a few model proteins, how such cooperation affects N-glycan modification and disulfide bonding at selective sites in individual proteins is largely unknown. Here, we reviewed the literature to discover the current status in understanding the relationships between NG and DBs in individual proteins. Our results showed that more than 2700 human proteins carry both PTMs, and fewer than 2% of them have been investigated in the associations between NG and DBs. We summarized both these proteins with the reported relationships in the two PTMs and the tools used to discover the relationships. We hope that, by exposing this largely understudied field, more investigations can be encouraged to unveil the hidden relationships of NG and DBs in the majority of membranes and secreted proteins for pathophysiological understanding and biotherapeutic development.     

Effect of lactulose on biotransformation of isoflavone glycosides to aglycones in soymilk by lactobacilli

ABSTRACT:  Lactobacillus acidophilus 4461, L. acidophilus 4962, L. casei 290, and L. casei 2607 were used to hydrolyze isoflavone glycosides (IG) to biologically active forms—isoflavone aglycones (IA)—in soymilk (SM) prepared from soy protein isolate (SPI) and soymilk supplemented with 0.5% (w/v) of lactulose (SML). L. acidophilus 4461 utilized the highest level of lactulose (3.01 mg/mL) and L. acidophilus 4962 utilized the least (0.86 mg/mL) at 24 h of incubation. The pH values decreased to 4.00 to 5.00 in SML, while they remained relatively high (6.15 to 6.36) in SM. Supplementation with lactulose significantly ( P < 0.05) enhanced the viable counts of all the 4 Lactobacillus strains. At the end of incubation, the viable counts of Lactobacillus ranged from 8.08 to 8.25 log CFU/mL in SML compared to 6.99 to 7.11 log CFU/mL in SM. Supplementation with lactulose increased the biotransformation of IG to IA after 6 h of incubation. The presence of lactulose in the medium enhanced the biotransformation level of IG to IA by Lactobacillus up to 21.9%. The hydrolysis level of malonyl genistin and acetyl genistin in SML was much higher than in SM by all the 4 probiotic organisms. The biotransformation of IG to IA occurred rapidly during the 1st 12 h of incubation in both SML and SM. Among the 4 Lactobacillus strains, L. acidophilus 4461 biotransformed the highest level (88.8%) of IG to IA in SML compared to 68.2% in SM after 24 h of incubation.     

Polyacrylonitrile‐carbon Nanotube‐polyacrylonitrile: A Versatile Robust Platform for Flexible Multifunctional Electronic Devices in Medical Applications

Flexible multifunctional electronic devices are of high interest for a wide range of applications including thermal therapy and respiratory devices in medical treatment, safety equipment, and structural health monitoring systems. This paper reports a scalable and efficient strategy of manufacturing a polyacrylonitrile‐carbon nanotube‐polyacrylonitrile (PAN‐CNT‐PAN) robust flexible platform for multifunctional electronic devices including flexible heaters, temperature sensors, and flexible thermal flow sensors. The key advantages of this platform include low cost, porosity, mechanical robustness, and electrical stability under mechanical bending, enabling the development of fast‐response flexible heaters with a response time of ≈1.5 s and relaxation time of ≈1.7 s. The temperature‐sensing functionality is also investigated with a range of temperature coefficient of resistances from ?650 to ?900 ppm K^?1. A flexible hot‐film sensing concept is successfully demonstrated using PAN‐CNT‐PAN with a high sensitivity of 340 mV (m s^?1)^?1. The sensitivity enhancement of 50% W^?1 is also observed with increasing supply power. The low cost, porosity, versatile, and robust properties of the proposed platform will enable the development of multifunctional electronic devices for numerous applications such as flexible thermal management, temperature stabilization in industrial processing, temperature sensing, and flexible/wearable devices for human healthcare applications.