Electrodepósito de níquel negro sobre aletas de cobre para aplicaciones en colectores solares planos

CIES2020 - XVII Congresso Ibérico e XIII Congresso Ibero-americano de Energia SolarRESUMEN: En este trabajo se reporta el desempeño de colectores solares construidos con aletas de cobre recubiertas con níquel/níquel negro con y sin SiO2. Los recubrimientos de níquel y níquel negro fueron obtenidos mediante electrodepósito y la capa de SiO2 por sol-gel y roció pirolítico, los resultados se comparan con un colector construido con un recubrimiento selectivo comercial TiNOX. Los resultados muestran que el níquel negro con SiO2 tiene una curva de desempeño cercana al colector construidos con el recubrimiento comercial. El recubrimiento de níquel negro con SiO2 fue obtenido por técnicas de bajo costo lo cual pudiera ser atractivo para las empresas dedicadas a la construcción de colectores solares.ABSTRACT: This work reports the performance of solar collectors built with nickel / black nickel coated copper fins with and without SiO2. The nickel and black nickel coatings were obtained by electrodeposition, the SiO2 layer by sol-gel and spray pyrolysis methods, the results are compared with a collector built with a commercial selective coating TiNOX. The results show that black nickel with SiO2 have a near performance curve than the collector built with the commercial coating. The black nickel coating with SiO2 was obtained by low cost techniques which could be attractive for companies dedicated to the construction of solar collectors.info:eu-repo/semantics/publishedVersio

Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)-associated inflammatory diseases.

BACKGROUND: Hyperzincemia and hypercalprotectinemia (Hz/Hc) is a distinct autoinflammatory entity involving extremely high serum concentrations of the proinflammatory alarmin myeloid-related protein (MRP) 8/14 (S100A8/S100A9 and calprotectin). OBJECTIVE: We sought to characterize the genetic cause and clinical spectrum of Hz/Hc. METHODS: Proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1) gene sequencing was performed in 14 patients with Hz/Hc, and their clinical phenotype was compared with that of 11 patients with pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome. PSTPIP1-pyrin interactions were analyzed by means of immunoprecipitation and Western blotting. A structural model of the PSTPIP1 dimer was generated. Cytokine profiles were analyzed by using the multiplex immunoassay, and MRP8/14 serum concentrations were analyzed by using an ELISA. RESULTS: Thirteen patients were heterozygous for a missense mutation in the PSTPIP1 gene, resulting in a p.E250K mutation, and 1 carried a mutation resulting in p.E257K. Both mutations substantially alter the electrostatic potential of the PSTPIP1 dimer model in a region critical for protein-protein interaction. Patients with Hz/Hc have extremely high MRP8/14 concentrations (2045 ± 1300 μg/mL) compared with those with PAPA syndrome (116 ± 74 μg/mL) and have a distinct clinical phenotype. A specific cytokine profile is associated with Hz/Hc. Hz/Hc mutations altered protein binding of PSTPIP1, increasing interaction with pyrin through phosphorylation of PSTPIP1. CONCLUSION: Mutations resulting in charge reversal in the y-domain of PSTPIP1 (E→K) and increased interaction with pyrin cause a distinct autoinflammatory disorder defined by clinical and biochemical features not found in patients with PAPA syndrome, indicating a unique genotype-phenotype correlation for mutations in the PSTPIP1 gene. This is the first inborn autoinflammatory syndrome in which inflammation is driven by uncontrolled release of members of the alarmin family