Influence of Alkaline Additives and Buffers on Mineral Trapping of CO2 under Mild Conditions

Carbon dioxide (CO₂) gas is the main contributor to climate change. CO₂ storage in underground brines and oil‐field brines by mineral trapping has been considered as a promising alternative in order to reduce CO₂ emissions. However, permanent storage of CO₂ in stable carbonate minerals is greatly dependent on brine pH, being favored over an alkaline pH. The effect of alkaline additives (NaOH, KOH, CaO) and buffer solutions (NaHCO₃/NaOH, Na₂HPO₄/NaOH, NH₄Cl/NH₄OH) on the mineral trapping of CO₂ under mild conditions using a synthetic brine is investigated. The results indicate that both NaOH+NH₄Cl/NH₄OH and KOH+NH₄Cl/NH₄OH mixtures promote precipitation mainly of calcium carbonate (CaCO₃).     

Synthesis and characterization of polyurethane/titanium dioxide nanocomposites obtained by in situ polymerization

The development of new polymeric and polymeric based materials is fundamental to meet the market demands. This work aims the synthesis and characterization of polyurethane/titanium dioxide nanocomposite, using low cost commercial raw materials. Nanocomposites were synthesized by in situ polymerization reactions in which titanium dioxide were added in the following proportions, by weight, in relation to the mass obtained from the pure polymer: 0.5, 1.0, 2.0, 3.0, 5.0, 7.0, and 10.0 %. These reactions were based in poli (ε-caprolactone) and 1,6-diisocyanatohexane. The materials were characterized by infrared spectroscopy Fourier transform, scanning electron microscopy, differential scanning calorimetry analysis, thermogravimetric analysis, dynamic mechanical thermal analysis, and UV–Vis spectroscopy. Based on the obtained results it was concluded that the nanocomposites synthesized by in situ polymerization presented, in general, thermal properties (degradation temperature) and mechanical properties higher than the pure polymer.     

Direct synthesis of dimethyl carbonate with supercritical carbon dioxide: Characterization of a key organotin oxide intermediate

The direct synthesis of dimethyl carbonate (DMC) using carbon dioxide as solvent and reagent for its fixation to methanol was explored with di-n-butyldimethoxystannane in order to get insight into the reaction mechanism for activity improvement. Catalytic runs including recycling experiments allowed isolation and characterization by NMR, IR, and single-crystal X-ray diffraction of a new tin complex containing 10 tin atoms. This compound could be prepared independently and is considered as a resting species. The yield of DMC is highest under 20 MPa pressure that fits with a monophasic supercritical medium in agreement with fluid phase equilibria calculations. In line, preliminary kinetics and initial rate determination show a positive order in carbon dioxide and a first-order dependence on the stannane. The initial rates were lower with the deca-tin complex than with the stannane precursor, but the turnover numbers (TONs) were higher. Water, the co-product of the reaction, was found to reversibly poison the active centers. Its in situ trapping had a beneficial effect. This study provides new mechanistic clues as to the reactive species and DMC formation. Further kinetics work is in progress to determine the rate-limiting step(s) at the initial stage of the reaction for more active catalyst design.     

Synthesis and characterization of waterborne polyurethane/ZnO composites

Waterborne polyurethane (WPU) is receiving great attention in recent decades mainly due to the possibility of the replacement of organic solvents by the water. However, this change causes a decrease in the properties (mechanical, thermal, adhesion, among others) of the films obtained by this technique. Therefore, studies have been carried out in the development of polymeric matrix with the incorporation of inorganic fillers. This work presents the synthesis by the in situ polymerization technique and the characterization of waterborne polyurethane/ZnO composites. These composites were based on isophorone diisocyanate, 2,2-bis(hydroxymethyl) propionic acid and a polyester diol (MM = 1,000 g/mol). The filler–polymer interaction, chemical structure, morphology, thermal and mechanical properties of the WPU/ZnO composites were investigated by Fourier transform infrared spectroscopy, Ultraviolet–visible spectroscopy, Thermogravimetric analysis, Differential scanning calorimetry, Scanning electron microscopy and Tensile testing. The results showed an improvement in thermal and mechanical properties of the PU/ZnO composites when compared with pure PU as well as good homogeneity of the filler into the polymer matrix.     

Synthetic Ni‐talc as filler for producing polyurethane nanocomposites

New synthetic Ni‐talc was used as filler in the synthesis of polyurethane (PU) nanocomposites by in situ polymerization and to emphasize the contribution of the new material compared with natural talc. Good dispersion of Ni‐talc was supported by homogeneous green coloration observed in the polymer matrix. X‐ray diffraction (XRD) analyses indicate the intercalation of polymeric matrix into the filler layers by the increase in d₀₀₁‐spacing value of the Ni‐talc for the nanocomposites when compared to the pristine filler. The nanocomposites obtained with synthetic talc showed an improvement in the crystallization temperature and in thermal stability when compared to pure PU and the composite obtained with natural talc. The young modulus of PU/talc materials containing both Ni‐talc and natural talc were slight higher than pure PU. As shown by scanning electron microscope (SEM), Ni‐talc fillers were well dispersed into the polymeric matrix probably due to the good compatibility of both phases filler/polymer mainly achieved by the filler OH interaction with the urethane group of the polymeric chain. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41854.     

Serum CA 242: the search for a valid marker of pancreatic cancer

As experience with peritoneal dialysis (PD) has improved and peritonitis rates have decreased, more patients are surviving for long periods on PD. Associated with this has been the recognition that there are unique complications of PD, specifically sclerosing syndromes and membrane failure that are most common in the long-term patient. Although anecdotal data would suggest that the long-term exposure to "bio-incompatable" fluids and or the occurrence of severe episodes of peritonitis are contributory in the pathogenesis of these diseases, cause and effect have not been proven. Normal peritoneal structure, changes that occur over time, and how the normal resident immune defense systems are altered with PD are reviewed. It is known that the continued loss of macrophages in the PD fluid results in an ever increasing percentage of immature cells in the peritoneum, which paradoxically are more reactive in terms of cytokine generation and less effective in host defense. The potential harmful effects of glucose and advanced glycosylation end products are also explored. The review concludes stating that further research is needed to better link the clinical syndromes with alterations in membrane structure/function.     

Investigation of degradation of polypropylene in soil using an enzymatic additive

Polypropylene (PP) has been widely used industrially in several sectors, mainly in the use of packaging of different products. Thus, this has been accumulated in our environment due to the incorrect disposal and its high resistance toward degradation, causing an array of environmental impacts. With this, one alternative that has been explored to minimize the problems intensified by these residues is the use of pro-degrading additives. Therefore, the aim of this work is to evaluate the degradation process of PP blends in soil using enzymatic additive. The soil degradation experiment was done for 6 months; monthly collected samples were checked for alterations on the material properties during that time. The extent of PP degradation with enzymatic additive was compared to an organic additive by techniques of FTIR, TGA, DSC, carbonyl index (CI), and crystallinity. From the obtained results it was observed that the additives influenced the degradation of PP. In addition, the enzymatic additive caused more significant changes in the CI (increase of 3693%), crystallinity (variation of 18.7%), and structural characteristics, indicating a greater influence on the degradation process in relation to the organic additive. In this way, this work has had an important role in the research and development of biodegradable materials with the aim of minimizing the effects induced by plastic waste in the environment.

     

Space anthropology: physical and cultural adaptation in outer space

Humans are the product of biologic and cultural adaptation to our Planet achieved over million years of Primates and Hominids species evolution which has led us to a specific development of intelligence, speech, and manual capability. Interface usability mainly depends on human characteristics that are also modified by variations in the environment. In outer space, body shapes may be different, things may not be in the expected place and models of conventional social relationships may be hardly transferred to prolonged missions. The process known as exaptation, according to which traits developed by a species as a response to a specific need are later “recycled” with new functions in a different environment, will be considered. Biologic and cultural built-in mechanisms belonging to our past cannot be left out in the analysis of design and man–machine interface in the Outer Space.     

Kinetic study of polyurethane synthesis using different catalytic systems of Fe,Cu, Sn,and Cr

This work presents a comparative study between alternative catalytic systems, metal‐β‐diketones complexes (iron, copper, chromium, and tin), and the commercial catalyst dibutyltin dilaurate, DBTDL, in the polyurethanes synthesis obtained from isophorone diisocyanate (IPDI) and polyols as polypropyleneglycol/diethyleneglycol and 1,6‐hexanodiol polyadipate (polyester A‐Mn = 2000 g/mol and polyester B‐Mn = 1000 g/mol) reactions. The polyurethanes synthesis was followed by the IPDI consumption in time, verified by infrared spectroscopy (FTIR) through the decrease of free NCO characteristic band at 2300–2200 cm^?1. The FTIR data was used to determine the polyurethanes formation kinetic behavior. It was verified that for the reactions with polyethers excess, DBTDL catalyst was more effective when compared to metal‐β‐diketones complexes, while for the reactions with polyester, A and B, the metal‐β‐diketones complexes were more effective. © 2009 Wiley Periodicals, Inc. JAppl Polym Sci, 2010     

Water treatment and monitor disinfection

Water treatment system and dialysis monitors are susceptible to microbial contaminations and periodical disinfection procedures are mandatory to obtain results requested from international standards and guidelines. Several chemical germicides or some physical treatments are on the market validated by device manufacturer according to medical device directives. With time, interfering substances from dialysis device or water are able to modify disinfection efficiency. Simulating-use testing is not a common procedure to validate disinfectants and recent data document as biofilm represents the most important cause of disinfection inefficacy. Some international standards include tests in the presence of various interfering substances but their use is not widespread. When using a disinfectant, residue toxicity, material compatibility and potential risks for the staff also have to be considered. A quality assurance program has to be implemented to obtain adequate performances and to improve results on patients.