Sugarcane bagasse fibers chemically modified on its surface were used to adsorb contaminants from biodiesel. Two biodiesel samples were used as adsorbates: crude and washed biodiesel. The contaminants were mainly glycerol and water, but also ions, and methanol. The biodiesel is usually washed, in order to remove most of the contaminants, but the procedure introduces large amounts of water, which are further difficult to remove, because the biodiesel acting as an acceptor of hydrogen bond. The adsorbent used in this work was proved to be very efficient to remove the contaminants and also to remove water from the washing the crude biodiesel. The contaminants adsorbed from biodiesel were identified by thermal analyses (DSC and DTA) of the fibers (adsorbent) and of the biodiesel (adsorbate) by comparing the results with the pure biodiesel. The proportion of free glycerol showed high adsorption efficiency for the crude biodiesel. A total amount of 1.34 g of fibers was estimated as being needed for its complete removal. The mass of bagasse fibers added (up to 1g) in a fixed volume of biodiesel was a relevant condition, as the saturation in fibers started at around 0.70 g cleaning up to about 98% removal of the impurities.

Resumo O objetivo desse estudo foi avaliar o grau de conversão, estabilidade de cor, composição química e resistência de união de um cimento resinoso fotoativado contaminado com três soluções hemostáticas diferentes. Foram preparadas amostras para o grupo controle (cimento não contaminado) e grupos experimentais (cimento contaminado com uma das soluções hemostáticas) de acordo com os testes. Para o grau de conversão e análise de cor (n=10), as amostras (3 mm de diâmetro e 2 mm de espessura) foram avaliadas por espectroscopia de infravermelho com transformação de Fourier (FTIR) e espectrofotometria CIELAB (L*, A*, B*), respectivamente. Para a análise química elementar (n=1), os espécimes (2 mm de espessura e 6 mm de diâmetro) foram avaliados por espectroscopia de energia dispersiva de raios-x (EDS). As resistências de união dos grupos foram avaliadas pelo ensaio de microcisalhamento (n=20) em um substrato cerâmico de vidro reforçado com leucita, seguida da análise de modo de falha por microscopia eletrônica de varredura (MEV). Os valores médios, com exceção da avaliação química e do modo de falha, foram avaliados por ANOVA e pelo teste de Tukey. A estabilidade de cor foi influenciada pelo tempo de armazenagem (p<0,001) e interação entre a contaminação e o tempo (p<0,001). A contaminação pelo Hemostop e Viscostat Clear não influenciaram no GC, porém a contaminação com Viscostat aumentou o GC. A resistência de união do cimento a cerâmica foi negativamente afetada pelos contaminantes (p<0,001). A contaminação por agentes hemostáticos afetou a resistência de união, o grau de conversão e a estabilidade de cor do cimento resinoso fotoativado testado.

Abstract The aim of this study was to evaluate the degree of conversion, color stability, chemical composition, and bond strength of a light-cured resin cement contaminated with three different hemostatic solutions. Specimens were prepared for the control (uncontaminated resin cement) and experimental groups (resin cement contaminated with one of the hemostatic solutions) according to the tests. For degree of conversion, DC (n = 5) and color analyses (n = 10), specimens (3 mm in diameter and 2 mm thick) were evaluated by Fourier transform infrared spectroscopy (FTIR) and CIELAB spectrophotometry (L*, a*, b*), respectively. For elemental chemical analysis (n = 1), specimens (2 mm thick and 6 mm in diameter) were evaluated by x-ray energy-dispersive spectroscopy (EDS). The bond strengths of the groups were assessed by the microshear test (n = 20) in a leucite-reinforced glass ceramic substrate, followed by failure mode analysis by scanning electron microscopy (SEM). The mean values, except for the elemental chemical evaluation and failure mode, were evaluated by ANOVA and Tukey’s HSD test. The color stability was influenced by storage time (p<0.001) and interaction between contamination and storage time (p<0.001). Hemostop and Viscostat Clear contamination did not affect the DC, however Viscostat increased the DC. Bond strength of the resin cement to ceramic was negatively affected by the contaminants (p<0.001). Contamination by hemostatic agents affected the bond strength, degree of conversion, and color stability of the light-cured resin cement tested.

Antibiotic resistance has been growing at an alarming rate and consequently the arsenal of effective antibiotics against Gram-negative and Gram-positive bacteria has dropped dramatically. In this sense there is a strong need to produce new substances that not only have good spectrum of activity, but having new mechanisms of action. In this regard, this paper emphasizes the coordination of metals to antibiotics as a strategy for reversing antibiotic resistance and production of new drugs, with a special focus on quinolones, fluoroquinolones, sulfonamides and tetracyclines.

Tetracyclines exhibits activity to a broad range of Gram-negative and Gram-positive bacteria and this fact allied to the low toxicity, low cost, and the advantage of administration by oral route led to their indiscriminate use, which caused the appearance of bacterial resistance to these agents, wich has restricted its clinical utility, though new applications have emerged. On the other hand, the glycylcyclines, semi-synthetic products are similar to tetracyclines, which are active against many bacteria resistant to tetracycline and other classes of antibiotics. The purpose of this paper is to give an overview of this important class of antibiotics focusing on its coordination chemistry and possible applications.

In this report, we studied the thickness effect on the optical and morphological properties of self-assembled (SA) poly(p-phenylenevinylene) (PPV) films, wich were processed with 5 and 75 layers from a PPV precursor polymer and dodecylbenzenesulfonate, and then, thermally converted at 230 °C. The increase of the film thickness yielded more intense peaks in the vibrational spectral range. The electron-phonon coupling was quantified by the Huang - Rhys factor, that shows the effects on the polymer chain mobility in the interface substrate/polymer. A strong emission anisotropy r=0.57 was observed for the film with 5 layers of thickness decreasing to 0.34 for the film with 75 layers. Finally, the surface topology of the films was measured using Atomic Force Microscopy.

Fibras de bagaço de cana-de-açúcar não alvejadas (FBC) e alvejadas com peróxido de hidrogênio (FBC-AP) foram enxertadas com o absorvedor de UV hidroxifenilbenzotriazol (1) e/ou com um radical nitróxido do tipo piperidiniloxi (3). As fibras FBC-AP foram também acetiladas com anidrido acético. A fotossensibilidade dessas fibras à radiação UV foi avaliada comparativamente, empregando coordenadas Lab color, assim como pela monitoração dos seus espectros de reflectância difusa no UV-Visível. As fibras FBC mostraram-se fotoestáveis, enquanto que as FBC-AP apresentaram certa sensibilidade à radiação UV. A estabilidade das FBC deve-se à presença de unidades do composto fotoestável p-hidroxifenilpropano, proveniente dos fragmentos de lignina. As fibras FBC enxertadas e não-enxertadas apresentam comportamentos similares frente à radiação UV e Visível enquanto que as FBC-AP enxertadas são fotoestabilizadas pela presença de 2 ou 4, ou ambos. A acetilação das fibras FBC-AP induz a fotoestabilização, em adição a certo efeito de fotoalvejamento. O fotoalvejamento foi também apresentado por medidas de emissão de fluorescência. Como conseqüência dessas observações, as fibras FBC devem ser consideradas como materiais lignocelulósicos com elevado potencial de aplicação em ambientes externos.

Unbleached (SCB) and peroxide bleached (PB-SCB) sugarcane bagasse fibers were grafted with hydroxyphenylbenzotriazole UV absorber (1) and/or hindered nitroxide radical of piperidinyloxy type (3). PB-SCB fibers were also acetylated with acetic anhydride. The photosensitivity of the various fibers to UV light was comparatively evaluated using Lab color coordinates and by monitoring their UV-Visible diffuse reflectance spectra. SCB fibers were found to be photostable whereas PB-SCB fibers presented some sensitivity to UV light. The stability of SCB fibers was attributed to the presence of photostable para-hydroxyphenylpropane units in SCB lignin. The grafted and non-grafted SCB fibers showed similar behaviors against UV-Visible light whereas grafted PB-SCB were photostabilized by the presence of 2 or 4 or both. Acetylation of PB-SCB fibers induced photostabilization in addition to some photobleaching effect. The photobleaching was also revealed by fluorescence emission studies. As a consequence of these observations, SCB fibers might be considered to have a high potential for lignocellulosic materials to be used outdoors.

We report a study of a new chemical synthetic route of polystyrene sulphonate (PSS) films doped with neodymium ion (Nd+3) from a neodymium nitrate solution. The UV-Vis-NIR spectrum presents an intense characteristic electronic transition at 800 nm and the infrared spectrum presents low definition bands as a result of Nd3+ coordination with PSS molecule. Additionally, the spectrum of Nd-PSS film presents the same line shape profile of Nd3+ salt in aqueous solution. Selective luminescence spectroscopy measures shows that the incorporation of neodymium ion introduces a red shift bands and a better line shape definition in UV luminescence compared to PSS film, decreasing the interaction between PSS aromatic groups. The near-infrared emission was observed in the large spectrum region from 600 to 800 nm; it is associated with the Nd3+ complex of PSS monomer.