335 research outputs found

    A Novel Global MPP Tracking of Photovoltaic System Based on Whale Optimization Algorithm

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    To harvest maximum amount of solar energy and to attain higher efficiency, photovoltaic generation (PVG) systems are to be operated at their maximum power point (MPP) under both variable climatic and partial shaded condition (PSC). From literature most of conventional MPP tracking (MPPT) methods are able to guarantee MPP successfully under uniform shading condition but fails to get global MPP as they may trap at local MPP under PSC, which adversely deteriorates the efficiency of Photovoltaic Generation (PVG) system. In this paper a novel MPPT based on Whale Optimization Algorithm (WOA) is proposed to analyze analytic modeling of PV system considering both series and shunt resistances for MPP tracking under PSC. The proposed algorithm is tested on 6S, 3S2P and 2S3P Photovoltaic array configurations for different shading patterns and results are presented. To compare the performance, GWO and PSO MPPT algorithms are also simulated and results are also presented. From the results it is noticed that proposed MPPT method is superior to other MPPT methods with reference to accuracy and tracking speed.Article History: Received July 23rd 2016; Received in revised form September 15th 2016; Accepted October 1st 2016; Available onlineHow to Cite This Article: Kumar, C.H.S and Rao, R.S. (2016) A Novel Global MPP Tracking of Photovoltaic System based on Whale Optimization Algorithm. Int. Journal of Renewable Energy Development, 5(3), 225-232.http://dx.doi.org/10.14710/ijred.5.3.225-23

    Enhanced Grey Wolf Optimizer Based MPPT Algorithm of PV System Under Partial Shaded Condition

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    Partial shading condition is one of the adverse phenomena which effects the power output of photovoltaic (PV) systems due to inaccurate tracking of global maximum power point. Conventional Maximum Power Point Tracking (MPPT) techniques like Perturb and Observe, Incremental Conductance and Hill Climbing can track the maximum power point effectively under uniform shaded condition, but fails under partial shaded condition. An attractive solution under partial shaded condition is application of meta-heuristic algorithms to operate at global maximum power point. Hence in this paper, an Enhanced Grey Wolf Optimizer (EGWO) based maximum power point tracking algorithm is proposed to track the global maximum power point of PV system under partial shading condition. A Mathematical model of PV system is developed under partial shaded condition using single diode model and EGWO is applied to track global maximum power point. The proposed method is programmed in MATLAB environment and simulations are carried out on 4S and 2S2P PV configurations for dynamically changing shading patterns. The results of the proposed method are analyzed and compared with GWO and PSO algorithms. It is observed that proposed method is effective in tracking global maximum power point with more accuracy in less computation time compared to other methods.Article History: Received June 12nd 2017; Received in revised form August 13rd 2017; Accepted August 15th 2017; Available onlineHow to Cite This Article: Kumar, C.H.S and Rao, R.S. (2017 Enhanced Grey Wolf Optimizer Based MPPT Algorithm of PV System Under Partial Shaded Condition. Int. Journal of Renewable Energy Development, 6(3), 203-212.https://doi.org/10.14710/ijred.6.3.203-21

    Wasserstein Distributionally Robust Look-Ahead Economic Dispatch

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    We consider the problem of look-ahead economic dispatch (LAED) with uncertain renewable energy generation. The goal of this problem is to minimize the cost of conventional energy generation subject to uncertain operational constraints. The risk of violating these constraints must be below a given threshold for a family of probability distributions with characteristics similar to observed past data or predictions. We present two data-driven approaches based on two novel mathematical reformulations of this distributionally robust decision problem. The first one is a tractable convex program in which the uncertain constraints are defined via the distributionally robust conditional-value-at-risk. The second one is a scalable robust optimization program that yields an approximate distributionally robust chance-constrained LAED. Numerical experiments on the IEEE 39-bus system with real solar production data and forecasts illustrate the effectiveness of these approaches. We discuss how system operators should tune these techniques in order to seek the desired robustness-performance trade-off and we compare their computational scalability

    Transitional B cell cytokines predict renal allograft outcomes

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    Early immunological biomarkers that predict rejection and chronic allograft loss are needed to inform preemptive therapy and improve long-term outcomes. Here, we prospectively examined the ratio of interleukin-10 (IL-10) to tumor necrosis factor–α (TNFα) produced by transitional-1 B cells (T1B) 3 months after transplantation as a predictive biomarker for clinical and subclinical renal allograft rejection and subsequent clinical course. In both Training (n = 162) and Internal Validation (n = 82) Sets, the T1B IL-10/TNFα ratio 3 months after transplantation predicted both clinical and subclinical rejection anytime in the first year. The biomarker also predicted subsequent late rejection with a lead time averaging 8 months. Among biomarker high-risk patients, 60% had early rejection, of which 48% recurred later in the first posttransplant year. Among high-risk patients without early rejection, 74% developed rejection later in the first year. In contrast, only 5% of low-risk patients had early and 5% late rejection. The biomarker also predicted rejection in an External Validation Set (n = 95) and in key patient subgroups, confirming generalizability. Biomarker high-risk patients exhibited progressively worse renal function and decreased 5-year graft survival compared to low-risk patients. Treatment of B cells with anti-TNFα in vitro augmented the IL-10/TNFα ratio, restored regulatory activity, and inhibited plasmablast differentiation. To conclude, the T1B IL-10/TNFα ratio was validated as a strong predictive biomarker of renal allograft outcomes and provides a rationale for preemptive therapeutic intervention with TNF blockade

    Detection, Mapping, and Quantification of Single Walled Carbon Nanotubes in Histological Specimens with Photoacoustic Microscopy

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    Contains fulltext : 110845.pdf (publisher's version ) (Open Access)AIMS: In the present study, the efficacy of multi-scale photoacoustic microscopy (PAM) was investigated to detect, map, and quantify trace amounts [nanograms (ng) to micrograms (microg)] of SWCNTs in a variety of histological tissue specimens consisting of cancer and benign tissue biopsies (histological specimens from implanted tissue engineering scaffolds). MATERIALS AND METHODS: Optical-resolution (OR) and acoustic-resolution (AR)--Photoacoustic microscopy (PAM) was employed to detect, map and quantify the SWCNTs in a variety of tissue histological specimens and compared with other optical techniques (bright-field optical microscopy, Raman microscopy, near infrared (NIR) fluorescence microscopy). RESULTS: Both optical-resolution and acoustic-resolution PAM, allow the detection and quantification of SWCNTs in histological specimens with scalable spatial resolution and depth penetration. The noise-equivalent detection sensitivity to SWCNTs in the specimens was calculated to be as low as approximately 7 pg. Image processing analysis further allowed the mapping, distribution, and quantification of the SWCNTs in the histological sections. CONCLUSIONS: The results demonstrate the potential of PAM as a promising imaging technique to detect, map, and quantify SWCNTs in histological specimens, and could complement the capabilities of current optical and electron microscopy techniques in the analysis of histological specimens containing SWCNTs

    PET Imaging of Soluble Yttrium-86-Labeled Carbon Nanotubes in Mice

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    The potential medical applications of nanomaterials are shaping the landscape of the nanobiotechnology field and driving it forward. A key factor in determining the suitability of these nanomaterials must be how they interface with biological systems. Single walled carbon nanotubes (CNT) are being investigated as platforms for the delivery of biological, radiological, and chemical payloads to target tissues. CNT are mechanically robust graphene cylinders comprised of sp(2)-bonded carbon atoms and possessing highly regular structures with defined periodicity. CNT exhibit unique mechanochemical properties that can be exploited for the development of novel drug delivery platforms. In order to evaluate the potential usefulness of this CNT scaffold, we undertook an imaging study to determine the tissue biodistribution and pharmacokinetics of prototypical DOTA-functionalized CNT labeled with yttrium-86 and indium-111 ((86)Y-CNT and (111)In-CNT, respectively) in a mouse model.The (86)Y-CNT construct was synthesized from amine-functionalized, water-soluble CNT by covalently attaching multiple copies of DOTA chelates and then radiolabeling with the positron-emitting metal-ion, yttrium-86. A gamma-emitting (111)In-CNT construct was similarly prepared and purified. The constructs were characterized spectroscopically, microscopically, and chromatographically. The whole-body distribution and clearance of yttrium-86 was characterized at 3 and 24 hours post-injection using positron emission tomography (PET). The yttrium-86 cleared the blood within 3 hours and distributed predominantly to the kidneys, liver, spleen and bone. Although the activity that accumulated in the kidney cleared with time, the whole-body clearance was slow. Differential uptake in these target tissues was observed following intravenous or intraperitoneal injection.The whole-body PET images indicated that the major sites of accumulation of activity resulting from the administration of (86)Y-CNT were the kidney, liver, spleen, and to a much less extent the bone. Blood clearance was rapid and could be beneficial in the use of short-lived radionuclides in diagnostic applications

    Treatment of Peritoneal Carcinomatosis by Targeted Delivery of the Radio-Labeled Tumor Homing Peptide 213Bi-DTPA-[F3]2 into the Nucleus of Tumor Cells

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    BACKGROUND: Alpha-particle emitting isotopes are effective novel tools in cancer therapy, but targeted delivery into tumors is a prerequisite of their application to avoid toxic side effects. Peritoneal carcinomatosis is a widespread dissemination of tumors throughout the peritoneal cavity. As peritoneal carcinomatosis is fatal in most cases, novel therapies are needed. F3 is a tumor homing peptide which is internalized into the nucleus of tumor cells upon binding to nucleolin on the cell surface. Therefore, F3 may be an appropriate carrier for alpha-particle emitting isotopes facilitating selective tumor therapies. PRINCIPAL FINDINGS: A dimer of the vascular tumor homing peptide F3 was chemically coupled to the alpha-emitter (213)Bi ((213)Bi-DTPA-[F3](2)). We found (213)Bi-DTPA-[F3](2) to accumulate in the nucleus of tumor cells in vitro and in intraperitoneally growing tumors in vivo. To study the anti-tumor activity of (213)Bi-DTPA-[F3](2) we treated mice bearing intraperitoneally growing xenograft tumors with (213)Bi-DTPA-[F3](2). In a tumor prevention study between the days 4-14 after inoculation of tumor cells 6x1.85 MBq (50 microCi) of (213)Bi-DTPA-[F3](2) were injected. In a tumor reduction study between the days 16-26 after inoculation of tumor cells 6x1.85 MBq of (213)Bi-DTPA-[F3](2) were injected. The survival time of the animals was increased from 51 to 93.5 days in the prevention study and from 57 days to 78 days in the tumor reduction study. No toxicity of the treatment was observed. In bio-distribution studies we found (213)Bi-DTPA-[F3](2) to accumulate in tumors but only low activities were found in control organs except for the kidneys, where (213)Bi-DTPA-[F3](2) is found due to renal excretion. CONCLUSIONS/SIGNIFICANCE: In conclusion we report that (213)Bi-DTPA-[F3](2) is a novel tool for the targeted delivery of alpha-emitters into the nucleus of tumor cells that effectively controls peritoneal carcinomatosis in preclinical models and may also be useful in oncology
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