On the use of standards for microarray lossless image compression

The interest in methods that are able to efficiently compress microarray images is relatively new. This is not surprising, since the appearance and fast growth of the technology responsible for producing these images is also quite recent. In this paper, we present a set of compression results obtained with 49 publicly available images, using three image coding standards: lossless JPEG2000, JBIG, and JPEG-LS. We concluded that the compression technology behind JBIG seems to be the one that offers the best combination of compression efficiency and flexibility for microarray image compression.     

A three-state model for DNA protein-coding regions

It is known that the protein-coding regions of DNA are usually characterized by a three-base periodicity. In this paper, we exploit this property, studying a DNA model based on three deterministic states, where each state implements a finite-context model. The experimental results obtained confirm the appropriateness of the proposed approach, showing compression gains in relation to the single finite-context model counterpart. Additionally, and potentially more interesting than the compression gain on its own, is the observation that the entropy associated to each of the three base positions of a codon differs and that this variation is not the same among the organisms analyzed.     

Glass transition improvement in epoxy/graphene composites

Graphene oxide nanoplatelets (GO) were prepared from expanded graphite (EG) and functionalized with triethylenetetramine (GO-TETA). The GO-TETA consisted of a few layers of graphene (~4–6 layers), as determined by atomic force microscopy and Raman spectroscopy. X-ray photoelectron spectroscopy showed that the TETA was covalently linked to the GO in the GO-TETA sample. Epoxy composites based on the diglycidyl ether of bisphenol A with TETA as a hardener and with 0.5–3.0 wt% additions of EG and GO-TETA were investigated. The results showed that the addition of the nanofillers led to an increase of ~20 °C in the glass transition temperature. A slight increase in the ratio of the elastic modulus/hardness of the nanocomposites was observed by nanoindentation tests carried out at a depth range of 300 nm–1.3 μm; these tests indicated a tendency of increased fracture toughness. Microindentation had an enhancement of 40 % in hardness for the 1 wt% composite with GO-TETA relative to the corresponding value for the neat epoxy.     

微波等离子体化学气相沉积法在硅片上同时生长碳化硅和金刚石

研究了衬底温度、核化密度、衬底表而预处理等工艺参数对微波等离子体化学气相沉积法在硅片上同时生长碳化硅和金刚石的影响.采用扫描电镜、X-射线衍射、喇曼光谱和红外光谱对样品进行了表征.结果表明:从高核化密度生长的金刚石膜中探测不到碳化硅;不论对硅衬底进行抛光预处理还是未抛光预处理,从低核化密度牛长的金刚石厚膜中总能探测到碳化硅.碳化硅生长在硅衬底上未被金刚石覆盖的地方,或者是在金刚石晶核之间的空洞处.碳化硅形成和金刚石生长是同时发生的两个竞争过程.此研究结果为制备金刚石和碳化砟复合材料提供了一种新的方法.     

The influence of different zeolitic supports on hydrogen production and waste degradation

The photocatalyst composition affects the chemical–physical properties and directly impacts photocatalytic activity, both in the hydrogen production and degradation of organic contaminants. In this work, the influence of zeolitic structures NaA, NaY, and ZSM-5 combined with a 10% active phase, TiO₂ catalyst doped with 1% copper, and cobalt cocatalysts was tested to mineralize the reactive blue dye (CI250) and to produce hydrogen by photocatalysis under ultraviolet radiation. The band gap energy was affected mainly by the cocatalyst, while the Brunauer-Emmett-Teller method (BET) area was affected by the zeolite structure as well as the X-ray diffraction (XRD). The most active catalyst was the Cu@TiO₂/NaY, which promoted a hydrogen production rate of 240 μmolH₂gcat⁻¹ using 10% ethanol (v/v) aqueous solution as a sacrificial agent and mineralization of 53% of the organic dye, followed by the catalysts impregnated on ZSM-5 zeolites, which had discolouration up to 50% and hydrogen evolution of 92.6 and 109.7 μmolH₂gcat⁻¹ for the catalyst doped with Cu and Co, respectively.     

Electrospun polymeric membranes: Potential removal of endocrine disrupting compounds using solid membrane extraction and filtration processes

The present study aims to prepare polymeric membranes by electrospinning to apply in the removal of estrone (E1), 17β-estradiol (E2), and 17α-ethinylestradiol (EE2) in aqueous samples. Polymeric membranes of polyamide-6 (PA6), polycaprolactone (PCL), polylactic acid (PLA), and poly (butylene adipate-co-terephthalate) (PBAT) were obtained, characterized, and tested as sorbent material in processes of solid membrane extraction (SME) and membrane filtration. The efficiencies of the membranes after washing and/or conditioning processes were compared. The characterizations showed membranes with nanometer-diameter threads (between 250 and 1200 nm, on average). The four membranes' morphology, chemical composition, and thermal stability were like previous works. PBAT membranes were considered the most effective SME technique as a differential, with 44%–71% removal. For the membrane filtration process, the highest removal values were obtained for the PBAT membrane (82%–91%), which was also efficient in filtering a surface water sample from River Guaíba. PBAT polymeric membrane effectively removes and recovers the studied hormones, lowering production costs and allowing internal and external modifications. These aspects demonstrate that the obtained membranes offer an efficient material in extracting E1, E2, and EE2, of high simplicity, low cost, and green chemistry.     

Effects of Grafting Maleic Anhydride onto Poly-ɛ-caprolactone on Facilitative Enzymatic Hydrolysis

Plastic waste is a global issue because it causes overflowing landfills and pollution, leading to environmental concerns. To address this crisis, materials that can be decomposed in the natural environment are introduced to replace conventional plastics. Poly-ɛ-caprolactone (PCL) is a commonly used plastic that can degrade in natural environments. However, owing to its hydrophobicity, its natural decomposition rate is low. In this study, PCL is modified with maleic anhydride (MA) (PCL-g-MA) to increase hydrophilicity and amorphous region for faster decomposition. To assess the hydrolysis in seawater, lipase hydrolysis is performed to compare the decomposition of PCL-g-MA and PCL. Consequently, in a Pseudomonas lipase-containing PBS solution, it takes 72 and 120 h for complete hydrolyze of PCL-g-MA and PCL, respectively. MA grafted onto PCL increases the amorphous region, where lipase can easily diffuse into PCL-g-MA. Morphological (FESEM and POM images), thermal (TGA and DSC), and structural (FTIR, XRD, and XPS) analyzes support the hydrolysis reaction. The mechanisms proposed in this study confirm that lipase hydrolysis starts in the amorphous regions and then transfers to the crystal regions. This hydrolysis progress is expected to facilitate the creation of eco-friendly low-cost PCL-g-MA composites with high-rate hydrolysis, such as bio-plastics and bio-fibers.