Structural coloration of chitosan coated cellulose fabrics by electrostatic self-assembled poly (styrene-methyl methacrylate-acrylic acid) photonic crystals

The structural coloration of a chitosan-coated woven cotton fabric obtained by glutaraldehyde-stabilized deposition of electrostatic self-assembled monodisperse and spherically uniform (250 nm) poly (styrene-methyl methacrylate-acrylic acid) photonic crystal nanospheres (P(St-MMA-AA)) was investigated. Bright iridescent coatings displaying different colors in function of the viewing angle were obtained. The SEM, diffuse reflectance spectroscopy, TGA, DSC and FTIR analyses confirm the presence of structural color and the glutaraldehyde and chitosan ability to provide durable chemical bonding between cotton fabric and photonic crystal (PCs) coating with the highest degradation temperature and the lowest enthalpy. The coatings are characterized by a mixture of face-centered cubic and hexagonal close-packed arrays alternating random packing regions. For the first time a cost-efficient structural coloration with high washing and light fastness using self-assembled P(St-MMA-AA) photonic crystals was successfully developed onto woven cotton fabric using chitosan and/or glutaraldehyde as stabilizing agent opening new strategies for the development of dye-free coloration of textiles.This work is supported by FEDER funding on the COMPETE program and by national funds through Portuguese Foundation for Science and Technology (FCT) within the scope of the project POCI-01-0145- FEDER- 007136 and UID/CTM/00264. A. Zille also acknowledge funding from FCT within the scope of the contract IF/00071/2015.info:eu-repo/semantics/publishedVersio

A flow system with in-line blank correction applied to the spectrophotometric determination of total iron and chromium (VI) in wastewaters

A flow system using the sample as the carrier with a propulsion device located after the detector is presented. This approach allows the correction of the intrinsic color of the sample, as it provides baseline adjustment for each sample. A confluence situated just after the selection valve allows the sample composition to be adjusted for the colorimetric measurement. The developed methodology was applied to the colorimetric determination of total Fe and Cr (VI) in wastewaters at 0.1–6.0 mg L–1 and 0.03–1.0 mg L–1, respectively. RSDs lower than 3% and a sampling rate of approximately 40 h–1 were obtaine

Use of a single air segment to minimise dispersion and improve mixing in sequential injection: turbidimetric determination of sulphate in waters

In this work, we propose the use of an air segment in a sequential injection system to simultaneously improve the overlapping of the stacked zones and minimise dispersion. This strategy was developed for the determination of sulphate in natural and wastewaters. Barium chloride was used as a precipitating agent and the turbidity of the suspension formed was measured at 420 nm. Analysis was performed without sample pre-treatment and the system was able to monitor sulphate concentration at a rate of at least 20 determinations per hour. Slightly different analytical sequences were developed for natural and wastewaters in order to minimise specific interferences. Direct determination of sulphate was possible within a concentration range of 10–100 and 16–100 mg SO42− L−1 for natural and wastewaters, respectively. Results obtained were comparable with those of the reference method with relative deviations lower than 5%. Relative standard deviations between 1.6% and 3.3% were found

Properties and controlled release of chitosan microencapsulated limonene oil

Chitosan microcapsules containing limonene essential oil as active ingredient were prepared by coacervation using three different concentrations of NaOH (0.50, 1.00, 1.45 wt%) and fixed concentrations of chitosan and surfactant of 0.50 wt%. The produced microcapsules were fully characterized in their morphology and chemical composition, and the kinetic release analysis of the active ingredient was evaluated after deposition in a non-woven cellulose fabric. The concentration of 1.00 and 1.45 wt% clearly show the best results in terms of dimension and shape of the microcapsules as well as in the volatility results. However, at the concentration of 1 wt% a higher number of microcapsules were produced as confirmed by FTIR and EDS analysis. Free microcapsules are spherical in size with disperse diameters between 2 and 12 μm. Immobilized microcapsules showed sizes from 4 to 7 μm, a rough surface and loss of spherical shape with pore formation in the chitosan walls. SEM analysis confirms that at higher NaOH concentrations, the larger the size of the microcapsules. This technique shows that by tuning NaOH concentration it is possible to efficiently control the release rate of encapsulated active agents demonstrating great potential as insect repellent for textiles.JMS and ALC acknowledge CAPES Foundation, the Ministry of Education of Brazil, Proc. no 8976/13-9 e Proc. No 1071/13-0, respectively, and the Department of Textile Engineering of the University of Minho, Portugal. J. Molina is grateful to the Conselleria d'Educacio, Formacio i Ocupacio (Generalitat Valenciana) for the Programa VALi+D Postdoctoral Fellowship. AZ (C2011-UMINHO-2C2T-01) acknowledges funding from Programa Compromisso para a Ciencia 2008, Portugal. Shafagh Dinparast Tohidi would like to thank the Portuguese Foundation of Science and Technology for providing the PhD grant SFRH/BD/94759/2013

On the constraints violation in forward dynamics of multibody systems

It is known that the dynamic equations of motion for constrained mechanical multibody systems are frequently formulated using the Newton-Euler’s approach, which is augmented with the acceleration constraint equations. This formulation results in the establishment of a mixed set of partial differential and algebraic equations, which are solved in order to predict the dynamic behavior of general multibody systems. The classical resolution of the equations of motion is highly prone to constraints violation because the position and velocity constraint equations are not fulfilled. In this work, a general and comprehensive methodology to eliminate the constraints violation at the position and velocity levels is offered. The basic idea of the described approach is to add corrective terms to the position and velocity vectors with the intent to satisfy the corresponding kinematic constraint equations. These corrective terms are evaluated as function of the Moore-Penrose generalized inverse of the Jacobian matrix and of the kinematic constraint equations. The described methodology is embedded in the standard method to solve the equations of motion based on the technique of Lagrange multipliers. Finally, the effectiveness of the described methodology is demonstrated through the dynamic modeling and simulation of different planar and spatial multibody systems. The outcomes in terms of constraints violation at the position and velocity levels, conservation of the total energy and computational efficiency are analyzed and compared with those obtained with the standard Lagrange multipliers method, the Baumgarte stabilization method, the augmented Lagrangian formulation, the index-1 augmented Lagrangian and the coordinate partitioning method.The first author expresses his gratitude to the Portuguese Foundation for Science and Technology through the PhD grant (PD/BD/114154/2016). This work has been supported by the Portuguese Foundation for Science and Technology with the reference project UID/EEA/04436/2013, by FEDER funds through the COMPETE 2020 – Programa Operacional Competitividade e Internacionalização (POCI) with the reference project POCI-01-0145-FEDER-006941.info:eu-repo/semantics/publishedVersio

A História da Alimentação: balizas historiográficas

Os M. pretenderam traçar um quadro da História da Alimentação, não como um novo ramo epistemológico da disciplina, mas como um campo em desenvolvimento de práticas e atividades especializadas, incluindo pesquisa, formação, publicações, associações, encontros acadêmicos, etc. Um breve relato das condições em que tal campo se assentou faz-se preceder de um panorama dos estudos de alimentação e temas correia tos, em geral, segundo cinco abardagens Ia biológica, a econômica, a social, a cultural e a filosófica!, assim como da identificação das contribuições mais relevantes da Antropologia, Arqueologia, Sociologia e Geografia. A fim de comentar a multiforme e volumosa bibliografia histórica, foi ela organizada segundo critérios morfológicos. A seguir, alguns tópicos importantes mereceram tratamento à parte: a fome, o alimento e o domínio religioso, as descobertas européias e a difusão mundial de alimentos, gosto e gastronomia. O artigo se encerra com um rápido balanço crítico da historiografia brasileira sobre o tema

Sequential injection standard addition system with a mixing chamber: determination of orthophosphate in waters

A sequential injection system based on the standard addition method using a single standard solution was developed. Successive additions of known amounts of analyte are made to the sample in a mixing chamber placed in a side port of the selection valve; other in-line sample treatments were also performed in the mixing chamber. The proposed method was evaluated by performing experiments with the bromothymol blue dye, and subsequently applied to the spectrophotometric determination of orthophosphate in wastewater, micro algae medium and fish farming water samples. The sample concentration is obtained after plotting a linear graph of analytical signal as a function of the standard mass added to the sample. For the determination of orthophosphate, relative standard deviations were lower than 4 % and the results were in agreement with those obtained by the reference metho

A double-line sequential injection system for the spectrophotometric determination of copper, iron, manganese, and zinc in waters

A double-line sequential injection system was developed for the spectrophotometric determination of several metal ions in waters. The proposed double-line configuration was used to enable adding sample and chromogenic reagents as merging zones. The methodology was applied to the spectrophotometric determination of copper, iron, manganese, and zinc in samples of diverse origins at the range of 0.15–5.00, 0.10–10.0, 0.48–4.00, and 0.11–5.00 mg/L, respectively. Different chromogenic reagents and detection wavelengths were used. The chromogenic reagents for iron and manganese were 1,10-phenanthroline and formaldoxime, respectively. Copper and zinc were both determined using the analytical reagent zincon. Analytical characteristics of the methodology, such as manifold parameters, buffer pH, and reagent concentrations were optimized, and interference of some of the metal ions commonly present in water sample was assessed. Results of the analysis were in agreement with those obtained by atomic absorption spectrometry. Repeatability, expressed as the relative standard deviation for 10 consecutive injections of water samples, was lower than 6%. The determination rate was approximately 36/h