Estrutura e algumas propriedades ópticas de difenilfosfinatos de terras-raras

Coordination compounds of trivalent lanthanides cations with diphenylphosphinate are originated from direct reaction between a lanthanide salt and diphenylphosphinic acid. These complexes have peculiar and intriguing features, as (i) quickly obtainment through wet process precipitation, (ii) appreciable thermal stability, similar to inorganic phosphates, (iii) polymeric structure, and consequently, (iv) low solubility in both polar and non-polar solvents. Nowadays, coordination polymers are classified as coordination networks or, in case of porous materials, as metal-organic frameworks (MOFs). By this study, we aim to determine some optical properties of rare-earth diphenylphosphinate (RE = La3+, Eu3+, Gd3+, Lu3+) and conduct an updated classification of these compounds, bringing more details of its structure and the possible proposal of new materials with applications in lighting, detection of ionizing radiation and magnetism. The complexes of trivalent rare-earth cation with diphenylphosphinate were prepared by direct mixture of diphenylphosphinic acid with rare-earth metal chloride, both in ethanolic solution. The solution of diphenylphosphinic acid was kept in a beaker under constant stirring with pH measurements of the solution and gadolinium chloride solution was then dripped slowly with the aid of a burette until its complete addition; the following metal:ligand molar ratios were tested: 1:1, 1:2, 1:3, 2:1 e 3:1. The compounds were characterized by spectroscopic and structural techniques. By Fourier Transform Infrared Spectroscopy (FT-IR), it was possible to check the total ionization of diphenylphosphinic acid in synthesized complexes, confirmed by the absence of the band type A, B, C related to ѵ(O-H) of the acid (2663 cm-1, 2168 cm-1, 1684 cm-1), as well as the disappearance of ѵ(P-OH)=961 cm-1. Furthermore, the occurrence of bands shifts of ѵ(POO-) [symmetrical and asymmetrical] of...

Relação entre a composição de condicionadores capilares e a formação de cristais líquidos

O Brasil é o terceiro maior consumidor de cosméticos no mundo, representando a segunda colocação em produtos de higiene capilar. Tal colocação está relacionada aos nossos padrões de cuidados estéticos capilares, que muitas vezes, provocam agressões físicas e químicas, deixando os cabelos danificados e quebradiços. Os condicionadores capilares tornam-se uma ferramenta interessante, devido aos inúmeros benefícios protetores oferecidos às superfícies dos fios. A presença de tensoativos catiônicos e álcoois graxos de cadeia longa, unidos à temperatura de fusão dos materiais, velocidade de agitação imposta e resfriamento adequado do produto, podem ser os responsáveis pela formação de cristais líquidos. Tais estruturas conferem estabilidade, viscosidade, melhorias na aparência estética e sensorial do produto e, devido a estas qualidades estão ganhando espaço no mercado cosmético. Assim, o objetivo do trabalho foi desenvolver e formular condicionadores capilares variando-se as concentrações e/ou os tensoativos catiônicos e álcoois graxos, visando obter estruturas líquido-cristalinas associadas aos condicionadores, através da técnica de microscopia de luz polarizada (MLP), caracterização das estruturas pela técnica de espalhamento de raios-X a baixo ângulo (SAXS) e analise do perfil de textura (TPA) das formulações. Foram manipuladas 14 emulsões O/A, variando-se os álcoois graxos de cadeia longa (16 a 18C) e ceras auto emulsionantes catiônicas. Os resultados da MLP foram, em sua maioria, positivos para a presença de estruturas na forma de cruz de malta. A técnica de SAXS confirmou os sistemas sugeridos pela MLP caracterizando a estrutura líquida cristalina do tipo lamelar. A TPA inferiu que a alta estabilidade física apresentada por estas emulsões, e seu particular desempenho no deslizamento dos cabelos, pode estar relacionada à presença de tal organização estrutural nas formulações...

Obtenção e caracterização de nanocelulose a partir de fibras de Chorisia speciosa St. Hil

Natural fibers have been highlighted as a renewable material that can replace materials from oil and its derivatives. In this context, Brazil becomes the perfect setting because of the diversity of fibers found in its territory, such as sugarcane, sisal, rice, cotton, coconut, pineapple, among others. The paineiras (Chorisia speciosa St. Hil) are typically Brazilian trees, which produce paina as fruit. These fruits are still little studied as a source of lignocellulose by research groups. This project aimed obtaining and characterization of cellulose nanofibers from the fibers from the paina fibers. Obtaining nanocellulose is practically made through simplified chemical processes. First, was performed out pre-treatments to removal of waxes, lignin and hemicellulose. The first stage of pre-treatment was carried out by alkaline aqueous solution of sodium hydroxide (NaOH) at 5wt%, where the fibers were under constant agitation for 1h at 70°C. Through alkali treatment it was possible to remove most of the lignin, hemicellulose, waxes and extractives. After the alkaline treatment was done bleaching with an aqueous solution of sodium hydroxide (NaOH) to 4wt% and hydrogen peroxide (H2O2) to 24wt% 1:1 during 2h with constant stirring to 50 °C. Through bleaching was possibe to remove residual lignin, and got cellulose with 72% of crystallinity. Nanocellulose of paina fibers was extracted using different conditions of acid hydrolysis with sulfuric acid (H2SO4) to 50wt%. After acid hydrolysis, the suspensions were centrifuged during 30 min and dialyzed in water to remove excess acid until neutral pH (6-7). Then the suspensions were passed by ultrasonification in an ultrasound 20 kHz during 1h in an ice bath. Untreated, alkalinized and bleached fibers as well as cellulose nanoparticles were characterized by the techniques of thermogravimetry ... (Complete abastract click electronic access below)

Avaliação histológica e funcional do enxerto de neotraqueia de coelho desenvolvido por bioengenharia

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)