Influence of end-group modification on interaction of amphiphilic poly(oxyethylene)-<Emphasis Type="Italic">b</Emphasis>-poly(oxybutylene) block copolymers with ionic surfactants

Amphiphilic poly(oxyethylene)-b-poly(oxybutylene) block copolymers having hydrophilic block end-capped with neutral dimethylamino (DE₇₉B₃₄) and cationic trimethyl ammonium (TE₇₉B₃₄) groups, respectively were investigated for their interactions with ionic surfactants, sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB) using tensiometry, conductometry and dynamic light scattering. The self-assembly of DE₇₉B₃₄ and TE₇₉B₃₄ occur at 0.7 g/dm³ and 0.8 g/dm³, respectively. TE₇₉B₃₄ binds favorably with oppositely charged SDS, causing a substantial change in surface tension compared to other surfactant-polymer systems. In mixed polymer-surfactant systems, the micellization was promoted in the presence of SDS, but it was suppressed with CTAB. Such behavior is expected for cationic block copolymers, since they can engage into ion-pair formation with anionic SDS. For neutral polymers, the behavior is reflective of surfactants’ head group hydrophobicity. The head groups of CTAB are more hydrophobic and their existence in the proximity of hydrophobic segments of polymers induces shape transition to non-spherical morphologies. Gibb’s free energy of adsorption at air – water interface is negative for SDS, CTAB and surfactant-block copolymer systems, indicating that the process is highly spontaneous. The increase in entropy of TE₇₉B₃₄ during micelle formation with temperature is due to disturbance of hydrophobic structure of water molecules, thus hydrophobic parts are removed from bulk solution to the interface and also in the interior of micelle the freedom of hydrophobic part is increased. The dynamic laser light scattering results revealed that due to presence of block copolymers pre-micellar aggregates were favored.     

Pathogen‐Mimicking MnO Nanoparticles for Selective Activation of the TLR9 Pathway and Imaging of Cancer Cells

Here, design of the first pathogen‐mimicking metal oxide nanoparticles with the ability to enter cancer cells and to selectively target and activate the TLR9 pathway, and with optical and MR imaging capabilities, is reported. The immobilization of ssDNA (CpG ODN 2006) on MnO nanoparticles is performed via the phosphoramidite route using a multifunctional polymer. The multifunctional polymer used for the nanoparticle surface modification not only affords a protective organic biocompatible shell but also provides an efficient and convenient means for loading immunostimulatory oligonucleotides. Since fluorescent molecules are amenable to photodetection, a chromophore (Rhodamine) is introduced into the polymer chain to trace the nanoparticles in Caki‐1 (human kidney cancer) cells. The ssDNA coupled nanoparticles are used to target Toll‐like receptors 9 (TLR9) receptors inside the cells and to activate the classical TLR cascade. The presence of TLR9 is demonstrated independently in the Caki‐1 cell line by western blotting and immunostaining techniques. The magnetic properties of the MnO core make functionalized MnO nanoparticles potential diagnostic agents for magnetic resonance imaging (MRI) thereby enabling multimodal detection by a combination of MR and optical imaging methods. The trimodal nanoparticles allow the imaging of cellular trafficking by different means and simultaneously are an effective drug carrier system.     

A NOMA-Enabled Cellular Symbiotic Radio for mMTC

Wireless Personal Communications - Non-orthogonal multiple access (NOMA) scheme, potentially enabling high spectral efficiency, is one of the key technological innovations in the 5th generation...     

Effect of Mg doping on the superconducting properties of Cu/sub 1-x/Tl/sub x/Ba/sub 2/Ca/sub 3-y/Mg/sub y/Cu/sub 4/O/sub 12-/spl delta//

Superconducting properties of Cu/sub 1-x/Tl/sub x/Ba/sub 2/Ca/sub 3-y/Mg/sub y/Cu/sub 4/O/sub 12-/spl delta// (Cu/sub 1-x/Tl/sub x/Mg/sub y/-1234) material have been studied in the composition range y=0,1.5,2.25. The zero resistivity critical temperature [T/sub c/(R=0)] was found to increase with the increased concentration of Mg in the unit cell; for y=1.5 [T/sub c/(R=0)]=131 K was achieved which is hitherto highest in Cu/sub 1-x/Tl/sub x/-based superconductors. The X-ray diffraction analyses have shown the formation of a predominant single phase of Cu/sub 0.5/Tl/sub 0.5/Ba/sub 2/Ca/sub 3-y/Mg/sub y/Cu/sub 4/O/sub 12-/spl delta// superconductor with an inclusion of impurity phase. It is observed from the convex shape of the resistivity versus temperature measurements that our as-prepared material was in the region of carrier over-doping, and the number of carriers was optimized by postannealing experiments in air at 400/spl deg/C, 500/spl deg/C, and 600/spl deg/C. The T/sub c/(R=0) was found to increase with postannealing and the best postannealing temperature was found to be 600/spl deg/C. The mechanism of increased T/sub c/(R=0) is understood by carrying out infrared absorption measurements. It was observed through softening of Cu(2)-O/sub A/-Tl apical oxygen mode that improved interplane coupling was a possible source of enhancement of T/sub c/(R=0) to 131 K.     

Joint routing,link capacity dimensioning,and switch port optimization for dynamic traffic in optical networks

This paper considers a challenging problem: to simultaneously optimize the cost and the quality of service in opaque wavelength division multiplexing (WDM) networks. An optimization problem is proposed that takes the information including network topology, traffic between end nodes, and the target level of congestion at each link/node in WDM networks. The outputs of this problem include routing, link channel capacities, and the optimum number of switch ports locally added/dropped at all switch nodes. The total network cost is reduced to maintain a minimum congestion level on all links, which provides an efficient trade-off solution for the network design problem. The optimal information is utilized for dynamic traffic in WDM networks, which is shown to achieve the desired performance with the guaranteed quality of service in different networks. It was found that for an average link blocking probability equal to 0.015, the proposed model achieves a net channel gain in terms of wavelength channels ( ) equal to 35.72 , 39.09 , and 36.93 compared to shortest path first routing and equal to 29.41 , 37.35 , and 27.47 compared to alternate routing in three different networks.     

Dehydrogenation of C3–C4 paraffin's to corresponding olefins over slit-SAPO-34 supported Pt-Sn-based novel catalyst

The objective of this work is to discuss the performance of Pt-Sn/slit-SAPO-34 novel catalyst for selective C₃–C₄ dehydrogenation to corresponding light olefins. The metallic contents, acidity, active metallic sites and metallic dispersion were determined using a number of physico-chemical techniques as it gives a justification for superior catalytic activity for dehydrogenation reaction. The Pt-Sn/slit-SAPO-34 catalyst was analyzed for dehydrogenation activity under optimized operating conditions; at atmospheric pressure, hydrogen to alkane (feed) molar ratio is 0.2, weight hourly space velocity 5 h^?1 and temperature 585 °C. Around 40% light alkane conversion and above 95% of total olefins selectivity with 94% propene, 92% n-butene and about 84% iso-butene selectivity were achieved over Pt-Sn/slit-SAPO-34 novel catalyst. The catalyst was parametrically characterized over the above said operating conditions and effects of operating conditions on product distribution were discussed. The coke formation was inherently related to catalyst activity in dehydrogenation reaction and related to surface intermetallic ensemble effects; and ultimately the prominent stakeholder in catalyst deactivation. The novel catalysts also showed very good hydrothermal stability in a continuous reaction–regeneration cycles due to silica-based acidic structure of support. The results obtained over Pt-Sn/slit-SAPO-34 novel catalyst were compared with other Pt-Sn-based ZSM-5 and SAPO-34 supported catalysts of similar active metallic content under identical operating conditions.