Photon and vibration synergism on planar defects induced 2D-graphitic carbon nitride for ultrafast remediation of dyes and antibiotic ampicillin

Journal of Materials Science - Hybrid oxidation methodologies (HOMs) and active site enrichment of 2D nanocatalyst through defects induction are ubiquitously used for generating adequate reactive...     

Approximation schemes for load balanced clustering in wireless sensor networks

Clustering sensor nodes is an efficient technique to improve scalability and life time of a wireless sensor network (WSN). However, in a cluster based WSN, the leaders (cluster heads) consume more energy due to some extra load for various activities such as data collection, data aggregation, and communication of the aggregated data to the base station. Therefore, balancing the load of the cluster heads is a crucial issue for the long run operation of the WSNs. In this paper, we first present a load balanced clustering scheme for wireless sensor networks. We show that the algorithm runs in O(nlogn) time for n sensor nodes. We prove that the algorithm is optimal for the case in which the sensor nodes have equal load. We also show that it is a polynomial time 2-approximation algorithm for the general case, i.e., when the sensor nodes have variable load. We finally improve this algorithm and propose a 1.5-approximation algorithm for the general case. The experimental results show the efficiency of the proposed algorithm in terms of the load balancing of the cluster heads, execution time, and the network life.     

Preparation of water-dispersible graphene by facile surface modification of graphite oxide

Water-dispersible graphene was prepared by reacting graphite oxide and 6-amino-4-hydroxy-2-naphthalenesulfonic acid (ANS). X-ray diffraction study showed that the basal reflection (002) peak of graphite oxide was absent in the ANS-functionalized graphene (ANS-G), indicating crystal layer delamination. Ultraviolet-visible spectral data were recorded to assess the solubility of the ANS-G in water. Fourier transform infrared spectral analysis suggested the attachment of ANS molecules to the surface of graphene. Raman and x-ray photoelectron spectroscopy revealed that oxygen functionality in the graphite oxide had been removed during reduction. Atomic force microscopy found that the thickness of ANS-G in water was about 1.8 nm, much higher than that of single layer graphene. Thermal stability measurements also indicated successful removal of oxygen functionality from the graphite oxide and the attachment of thermally unstable ANS to the graphene surfaces. The electrical conductivity of ANS-G, determined by a four-point probe, was 145 S m(-1) at room temperature.     

An economic design model for X¯ charts with random sampling policies

Recent literature contains many papers on the study of variable (but deterministic) sampling interval (VSI) policies for X¯ control charts. VSI policies perform better than their corresponding classical fixed-sampling-interval (FSI) policies. Results are also available in the literature for an adaptive VSI policy, an enhancement of the VSI policy, where the sample size also changes with the sampling interval. However, for many industrial (especially continuous) processes where X¯ charts are used, maintaining deterministic time intervals between samples is not possible owing to inherent randomness of the processes. In this paper we propose a new variable sampling policy, named random sampling policy (RSP), for X¯ charts in which the sampling intervals and the sample sizes (considered a function of the sampling intervals) are treated as random variables. An economic modeling framework for design of RSP with run rules is developed. Within the proposed modeling framework, special cases of RSP, such as VSI and FSI policies with and without run rules, can also be evaluated. An application of the economic model is demonstrated through design of RSP parameters for two numerical example problems.     

Rubber/LDH nanocomposites by solution blending

The rubber nanocomposites containing ethylene vinyl acetate (EVA) having 60 wt % of vinyl acetate content and organomodified layered double hydroxide (DS‐LDH) as nanofiller have been prepared by solution intercalation method and characterized. The XRD and TEM analysis demonstrate the formation of completely exfoliated EVA/DS‐LDH nanocomposites for 1 wt % filler loading followed by partially exfoliated structure for 5–8 wt % of DS‐LDH content. EVA/DS‐LDH nanocomposites show improved mechanical properties such as tensile strength (TS) and elongation at break (EB) in comparison with neat EVA. The maximum value of TS (5.1 MPa) is noted for 3 wt % of DS‐LDH content with respect to TS value of pure EVA (2.6 MPa). The data from thermogravimetric analysis show the improvement in thermal stability of the nanocomposites by ≈15°C with respect to neat EVA. Limiting oxygen index measurements show that the nanocomposites act as good flame retardant materials. Swelling property analysis shows improved solvent resistance behavior of the nanocomposites (1, 3, and 5 wt % DS‐LDH content) compared with neat EVA‐60. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Structural,microstructural, and thermal characterizations of a chalcopyrite concentrate from the Singhbhum shear zone,India

The structural and morphological characterizations of a chalcopyrite concentrate, collected from the Indian Copper Complex, Ghatshila, India, were carried out by X-ray diffraction, scanning electron mi...     

All‐Organic,Temporally Pure White Afterglow in Amorphous Films Using Complementary Blue and Greenish‐Yellow Ultralong Room Temperature Phosphors

Organic molecules exhibiting afterglow emission (lifetime longer than 0.1 s) under ambient conditions have sparked tremendous attention in recent years as a sustainable energy source with potential applications in displays, lighting, and bioimaging. However, white afterglow organic materials with color purity during the entire period of delayed emission, after the cessation of excitation source, are yet to be achieved due to the different excited state lifetimes of its primary or complementary components. Herein, a remarkable, ambient “temporally pure white afterglow,” which lasts for over 7 s, by coorganizing complementary blue and greenish‐yellow organic room temperature phosphors with similar ultralong lifetimes and efficiency, in an amorphous polymer film is demonstrated. One of the most efficient blue afterglow room temperature phosphors is also reported, with an ultralong lifetime up to 2.26 s and maximum quantum efficiency of 36.8%, from purely organic triazatruxenes en route to the realization of this white afterglow. Further, broad and complementary absorption features of the coorganized phosphors in the visible region facilitates an excitation‐dependent dynamic color‐tuning of the afterglow from sky‐blue to greenish‐yellow.     

Coverage and connectivity aware energy efficient scheduling in target based wireless sensor networks: an improved genetic algorithm based approach

Wireless Networks - Energy efficient scheduling of sensor nodes is one of the most efficient techniques to extend the lifetime of the wireless sensor networks (WSNs). Instead of activating all the...     

Synthesis and characterization of polyurethane/Mg‐Al layered double hydroxide nanocomposites

Layered double hydroxide (LDH) is a new type of nanofiller, which improves the physicochemical properties of the polymer matrix. In this study, 1, 3, 5, and 8 wt % of dodecyl sulfate‐intercalated LDH (DS‐LDH) has been used as nanofiller to prepare a series of thermoplastic polyurethane (PU) nanocomposites by solution intercalation method. PU/DS‐LDH composites so formed have been characterized by X‐ray diffraction and transmission electron microscopy analysis which show that the DS‐LDH layers are exfoliated at lower filler (1 and 3 wt %) loading followed by intercalation at higher filler (8 wt %) loading. Mechanical properties of the nanocomposite with 3 wt % of DS‐LDH content shows 67% improvement in tensile strength compared to pristine PU, which has been correlated in terms of fracture behavior of the nanocomposites using scanning electron microscope analysis. Thermogravimetric analysis shows that the thermal stability of the nanocomposite with 3 wt % DS‐LDH content is ≈ 29°C higher than neat PU. Limiting oxygen index of the nanocomposites is also improved from 19 to 23% in neat PU and PU/8 wt% DS‐LDH nanocomposites, respectively. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009