off-State Degradation in Drain-Extended NMOS Transistors: Interface Damage and Correlation to Dielectric Breakdown

Off-state degradation in drain-extended NMOS transistors is studied. Carefully designed experiments and well-calibrated simulations show that hot carriers, which are generated by impact ionization of surface band-to-band tunneling current, are responsible for interface damage during off-state stress. Classical on-state hot carrier degradation has historically been associated with broken equivSi-H bonds at the interface. In contrast, the off-state degradation in drain-extended devices is shown to be due to broken equivSi-O- bonds. The resultant degradation is universal, which enables a long-term extrapolation of device degradation at operating bias conditions based on short-term stress data. Time evolution of degradation due to broken equivSi-O- bonds and the resultant universal behavior is explained by a bond-dispersion model. Finally, we show that, under off-state stress conditions, the interface damage that is measured by charge-pumping technique is correlated with dielectric breakdown time, as both of them are driven by broken equivSi-O- bonds.     

Device Design and Optimization Considerations for Bulk FinFETs

Fabrication of FinFETs using bulk CMOS instead of silicon on insulator (SOI) technology is of utmost interest as it reduces the process costs. Using well-calibrated device models and 3-D mixed mode simulations, we show that bulk FinFETs can be optimized with identical performances as that of SOI FinFETs. Optimized bulk FinFETs are compared with the corresponding SOI FinFETs for a range of technology nodes using an extensive simulation and design methodology. Further, we extend the concept of body doping in bulk FinFETs to the case of lightly doped fins unlike the heavily doped fin cases reported earlier. The optimum body doping required for bulk FinFETs, and its multiple advantages are also systematically evaluated. We also show that device parasitics play a crucial role in the optimization of nanoscale bulk FinFETs.     

Improved Merkle Hash Tree-Based One-Time Signature Scheme for Capability-Enhanced Security Enforcing Architecture for Named Data Networking

The concept of network caching is determined to be the potential requirement of named data networks (NDN) for enhancing the capabilities of the traditional IP networking. It is responsible for location independent data accesses and optimal bandwidth utilization in multi-path data dissemination. However, the network caching process in NDN introduces security challenges such as content cache poisoning, malicious injection or flooding of the packets and violation in accessing content packets. In this paper, an Improved Merkle Hash Tree-based one-time signature scheme for capability-enhanced security enforcing architecture (IMHT-OTSS-CSEA) is proposed for provisioning data authenticity in a distributed manner for leveraging the capabilities to inform the access privileges of the packets during the process of data dissemination. It is proposed for permitting the routers to verify the forwarded packets’ authenticity in NDN. It is capable in handling the issues that emerge from unsolicited packets during a flooding-based denial of service attacks by supporting the indispensable verification process in routers that confirms the timeliness of packets. The simulation experiments conducted using the open source CCNs platform and Planetlab confirmed a significant mean reduction in delay of 14.61%, superior to the benchmarked schemes. It is identified to minimize the delay incurred in generating bit vectors by a average margin of 13.06%, excellent to the baseline approaches. It also confirmed a mean increase in the true positive rate of 5.42%, a mean increase in the precision rate of 6.04%, decrease in false positive rate of 6.82% and increase in F-measure of 5.62% compared to the baseline approaches in the context of detecting content cache pollution attack respectively.

     

Improved area—energy targeting for fired heater integrated heat exchanger networks

Effective integration of various subsystems into the overall process, results in an energy efficient and economic plant design. In this paper, issues related to the area-energy targeting for fired heater integrated heat exchanger networks are studied. Performance of a fired heater is affected by the variables such as fuel fired and air-preheat temperature. These variables along with the minimum approach temperature difference for the heat recovery of the background process, affect the performance of the overall system. A methodology is proposed for the area-energy targeting for fired heater integrated processes. In the proposed methodology, the fired heater heat duty split between the radiation and the convection section is determined using the one gas zone furnace model.     

Model-based control of titer and glycosylation in fed-batch mAb production: Modeling and control system development

Therapeutic monoclonal antibodies (mAbs) are typically manufactured using mammalian cell cultures in fed-batch bioreactors, with increasing emphasis on meeting productivity and product quality attribute targets that depend strongly on such process variables as nutrient feed rates and bioreactor operating conditions. In this article, we identify, categorize, and address the challenges of achieving both productivity and product quality goals simultaneously, by developing a multivariable, model-based control system that can satisfy multiple production objectives in a fed-batch cell culture process. Here, we discuss model development and present theoretical concepts of observability and controllability that are essential to understanding and handling effectively these intrinsic challenges. Subsequently, we evaluate via simulation the performance of the outer-loop model predictive control and demonstrate the overall capability to satisfy complex production objectives in a laboratory scale bioreactor, as a first step toward the ultimate goal of creating an advanced control system for fed-batch mAb manufacturing processes.     

Melt‐compounded natural rubber nanocomposites with pristine and organophilic layered silicates of natural and synthetic origin

Composites based on natural rubber (NR) and containing organophilic and pristine layered silicates of natural and synthetic origin were produced by melt compounding and sulfur curing. The curing, thermomechanical, and mechanical properties of the mixes, which contained 10 phr (parts per hundred parts of rubber) silicates, were determined. The dispersion of the silicates was studied by X‐ray diffraction (XRD) and transmission electron microscopy (TEM). Organophilic clays accelerated the sulfur curing of NR, which was believed to occur because of a complexation reaction in which the amine groups of the clay intercalants participated. The property improvements caused by the fillers were ranked as follows: organophilic clays > pristine synthetic layered silicate (sodium fluorohectorite) > pristine natural clay (purified sodium bentonite) > precipitated nonlayered silica (used as a reference). This was attributed to partial intercalation of the organophilic clay by NR on the basis of XRD and TEM results and to the high aspect ratio of the fluorohectorite. Apart from intercalation, severe confinement (i.e., the collapse of the interlayer distance) of the organoclays was observed. This peculiar feature was traced to the formation of a zinc coordination complex, which extracted the amine intercalant of the organoclays, thus causing the collapse of the layers. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 813–819, 2004     

Natural rubber–isotactic polypropylene thermoplastic blends

Thermoplastic elastomers, prepared by melt blending of natural rubber (NR) and isotactic polypropylene (PP) through a dynamic vulcanization technique, were developed during the later 1970s. However, they have certain drawbacks due to thermal degradation and higher molecular weight of NR. In the study reported here, NR was masticated to different levels prior its addition to isotactic polypropylene to improve the flow properties and to reduce the incompatibility resulting from molecular weight mismatch of NR/PP thermoplastic blends. Mixing energy curves of uncrosslinked blends and those of dynamically vulcanized blends crosslinked using different cure systems were compared. The mixing energy curves of blends containing NR of different molecular weight (M _n) and two grades of PP (injection and film grades) were also compared. Technological and processing properties of the dynamically vulcanized (sulphur and peroxide cure systems) and unvulcanized blends were compared with those of the samples containing unmasticated NR. The results indicated that a number average molecular weight in the range 4 × 10⁵ for NR increased the procoessability without significantly affecting the technological properties of NR/PP thermoplastic blends. Among the three cure systems studied Luperox 101 and dicumyl peroxide gave better technological properties than the sulphur‐cured samples. Two antioxidants, viz. quinoline (TDQ) and imidazole (MBI) type, were tried in NR/PP blends. It was found that TDQ imparts better aging resistance compared to MBI. The improvement in processability due to the reduction in molecular weight of natural rubber by mastication is more noticeable in the case of peroxide vulcanized blends compared to sulphur vulcanized samples. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2063–2068, 2004     

Characterization of Europium Complex-doped PMMA and PMMA-EVA Polymer Networks

Europium-β-diketone chelate doped poly(methyl methacrylate) and poly(methyl methacrylate)/poly(ethylene co-vinyl acetate) blends have been successfully prepared and characterized. The mechanical properties of the PMMA-EVA systems have been assessed in terms of tensile strength and impact strength. The thermal characteristics and the energy involved in thermal decomposition have been studied. The structural properties of the complex doped polymeric systems reveal that the complex exists in the same crystalline state in the doped systems as it does in the pure state. The orientations of the groups in the host matrix have been found to be affected by the complex loading. The optical properties of the system have been studied by photo luminescence spectroscopy. The fluorescence lifetime have been observed to decrease at greater loadings of the complex; an effect that has been attributed to concentration quenching. The complex doped PMMA/EVA polymer network developed is considered to be a potential candidate for the development of optoelectronic devices those possess superior mechanical properties.     

Removal of Poly Aromatic Hydrocarbons (PAHs) from Water: Effect of Nano and Modified Nano-clays as a Flocculation Aid and Adsorbent in Coagulation-flocculation Process

Water treatment process involving simultaneous action of adsorption on different nano and organo-modified nano-clays followed by coagulation-flocculation by alum and poly aluminium chloride (PAC) has been evaluated for the removal of PAHs (naphthalene, acenaphthalene, phenanthrene, fluoranthene, anthracene, and pyrene) from water. When clay minerals along with alum and PAC were used for treatment, 37.4–100.0% removal of PAHs was observed compared to 20–38% removal using normal water treatment process with either alum or alum + PAC. The effectiveness of clay minerals for removal of PAHs followed the order (P < 0.05): halloysitenano-clay (HN-clay) < normal bentonite (NB-clay) < hydrophilic nano-bentonite (HNB-clay) < nano-montmorillonite modified with dimethyl dialkyl amine (DMDA-M-clay) ≈ nano-montmorillonite modified with octadecylamine and aminopropyltriethoxysilane (ODAAPS-M-clay) ≈ nano-montmorillonite modified with octadecylamine (ODA-M-clay) in combination with alum + PAC. The modified treatment process (alum + PAC + clay minerals), where water was initially treated with clays followed by normal process of coagulation (alum + PAC), was found to be the most effective method with maximum removal for ODAAPS-M-clay (97.7–100.0%) which is at par wih ODA-M (97.0–100.0%), and DMDA-M-clay (94.8–100%). The removal of PAHs varied in the order: naphthalene ≈ acenaphthalene > anthracene ≈ pyrene > phenanthrene > fluoranthrene. The treatment combination having the maximum removal capacity was also used eficiently for the removal of PAHs from natural and fortified natural water. This article demonstrated adsorption-coagulation integrated system has the potential to remediate PAHs polluted water.