12 research outputs found

    A Novel Optimization Method for a Multi-Year Planning Scheme of an Active Distribution Network in a Large Planning Zone

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    Electric power distribution networks plays a significant role in providing continuous electrical energy to different categories of customers. In the context of the present advancements, future load expansion in the active distribution networks (ADNs) poses the key challenge of planning to be derived as a multi-stage optimization task, including the optimal expansion planning scheme optimization (EPSO). The planning scheme optimization is a multi-attribute decision-making issue with high complexity and solving difficulty, especially when it involves a large-scale planning zone. This paper proposes a novel approach of a multi-year planning scheme for the effective solution of the EPSO problem in large planning zones. The proposed approach comprises three key parts, where the first part covers two essential aspects, i.e., (i) suggesting a project condition set that considers the elements directly related to a group of specific conditions and requirements (collectively referred to as conditions) to ADN planning projects; and (ii) Developing a condition scoring system to evaluate planning projects. The second part of our proposed scheme is a quantization method of correlativity among projects based on two new concepts: contribution index (CI) and dependence index (DI). Finally, considering the multi-year rolling optimization, a detailed mathematical model of condition evaluation and spatiotemporal optimization sequencing of ADN planning projects is developed, where the evaluation and optimization are updated annually. The proposed model has been successfully validated on a practical distribution network located in Xiantao, China. The investigated case study and comparisons verify the various advantages, suitability, and effectiveness of the proposed planning scheme, consequently saving more than 10% of the investment compared with the existing implemented scheme

    Noise exposure in occupational setting associated with elevated blood pressure in China

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    Abstract Background Hypertension is the primary out-auditory adverse outcome caused due to occupational noise exposure. This study investigated the associations of noise exposure in an occupational setting with blood pressure and risk of hypertension. Methods A total of 1,390 occupational noise-exposed workers and 1399 frequency matched non-noise-exposed subjects were recruited from a cross-sectional survey of occupational noise-exposed and the general population, respectively. Blood pressure was measured using a mercury sphygmomanometer following a standard protocol. Multiple logistic regression was used to calculate the odds ratio (OR) and 95% confidence interval (CI) of noise exposure adjusted by potential confounders. Results Noise-exposed subjects had significantly higher levels of systolic blood pressure(SBP) (125.1 ± 13.9 mm Hg) and diastolic blood pressure (DBP) (77.6 ± 10.7 mm Hg) than control subjects (SBP: 117.2 ± 15.7 mm Hg, DBP: 70.0 ± 10.5 mm Hg) (P  0.05). Conclusions Occupational noise exposure was associated with higher levels of SBP, DBP, and the risk of hypertension. These findings indicate that effective and feasible measures should be implemented to reduce the risk of hypertension caused by occupational noise exposure

    Screening of noise-induced hearing loss (NIHL)-associated SNPs and the assessment of its genetic susceptibility

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    Abstract Background The aim of this study was to screen for noise-induced hearing loss (NIHL)-associated single nucleotide polymorphisms (SNPs) and to construct genetic risk prediction models for NIHL in a Chinese population. Methods Four hundred seventy-six subjects with NIHL and 476 matched controls were recruited from a cross-sectional survey on NIHL in China. A total of 83 candidate SNPs were genotyped using nanofluidic dynamic arrays on a Fluidigm platform. NIHL-associated SNPs were screened with a multiple logistic model, and a genetic risk model was constructed based on the genetic risk score (GRS). The results were validated using a prospective cohort population. Results Seven SNPs in the CDH23, PCDH15, EYA4, MYO1A, KCNMA1, and OTOG genes were significantly (P  0.05 and P < 0.1) associated with the risk of NIHL. A positive correlation was observed between GRS values and odds ratio (OR) for NIHL. Two SNPs, namely, rs212769 and rs7910544, were validated in the cohort study. Subjects with higher GRS (≧9) showed a higher risk of NIHL incidence with an OR of 2.00 (95% CI = 1.04, 3.86). Conclusions Genetic susceptibility plays an important role in the incidence of NIHL. GRS values, which are based on NIHL-associated SNPs. GRS may be utilized in the evaluation of genetic risk for NIHL and in the determination of NIHL susceptibility

    Neocortex- and hippocampus-specific deletion of Gabrg2 causes temperature-dependent seizures in mice

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    Mutations in the GABRG2 gene encoding the γ-aminobutyric acid (GABA) A receptor gamma 2 subunit are associated with genetic epilepsy with febrile seizures plus, febrile seizures plus, febrile seizures, and other symptoms of epilepsy. However, the mechanisms underlying Gabrg2-mediated febrile seizures are poorly understood. Here, we used the Cre/loxP system to generate conditional knockout (CKO) mice with deficient Gabrg2 in the hippocampus and neocortex. Heterozygous CKO mice (Gabrg2fl/wtCre+) exhibited temperature-dependent myoclonic jerks, generalised tonic-clonic seizures, increased anxiety-like symptoms, and a predisposition to induce seizures. Cortical electroencephalography showed the hyperexcitability in response to temperature elevation in Gabrg2fl/wtCre+ mice, but not in wild-type mice. Gabrg2fl/wtCre+ mice exhibited spontaneous seizures and susceptibility to temperature-induced seizures. Loss of neurons were observed in cortical layers V–VI and hippocampus of Gabrg2fl/wtCre+ mice. Furthermore, the latency of temperature- or pentylenetetrazol-induced seizures were significantly decreased in Gabrg2fl/wtCre+ mice compared with wild-type mice. In summary, Gabrg2fl/wtCre+ mice with Gabrg2 deletion in the neocortex and hippocampus reproduce many features of febrile seizures and therefore provide a novel model to further understand this syndrome at the cellular and molecular level

    Dehydration of Glycerol to Acrolein over Hierarchical ZSM‑5 Zeolites: Effects of Mesoporosity and Acidity

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    Selective dehydration of glycerol to value-added acrolein is an interesting catalytic process not only owing to the increasing coproduction of glycerol in the biodiesel production but also due to the emerging perspectives to provide a sustainable route for acrolein production. The use of zeolites in glycerol dehydration is a very promising way with high performance, but these microporous catalysts are often severely constrained by the rapid catalyst deactivation due to coke formation. Although the introduction of hierarchical structure in microporous zeolite crystals is believed to be an effective approach to enhance their activity and lifetime, the relationship between the mesoporosity and catalytic performance is still controversial. In this paper, four kinds of typical hierarchical ZSM-5 catalysts with diverse mesoporosity and similar microporosity/acidity are prepared by the salt-aided seed-induced route. By systematically studying their catalytic performances, the effects of various mesopore types on the glycerol dehydration are declared, including pore size, amount, distribution, and connectivity. The sample with open and interconnected mesopore architecture display the high activity, long lifetime, and improved selectivity, while the worse behavior of closed and small mesopores is attributed to the mass transfer limitations and/or the in-pore condensation of reactant or its heavier derivatives. Moreover, the combined effect of acidity and hierarchical structure was also explored by changing the framework Si/Al ratio. The findings emphasize the necessity of reasonably designing the zeolite catalysts with proper hierarchical structure and acidity for maximal catalytic advantage
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