The mantle mass flow interconnected with the process of Glacial Isostatic Adjustment (GIA) and the reformation of the Earth’s crust constantly perturbs the observed gravity field towards a hypothetic isostatic state. We analyse the temporal changes of the gravity field from the GRACE data, using different mathematical and/or statistical methods to detect the GIA amidst other gravity signals. A number of gravimetric post-glacial land uplift rate (LUR) modelling methods are investigated and compared with the data from a total number of 515 GPS stations and preferred GIA forward models in Fennoscandia and North America. We investigate three mathematical methods, namely regression, principal component, and independent component analysis (ICA) to extracting the GIA signal from the GRACE monthly geoid heights. We use some regularization techniques to exploit the GRACE monthly data to their maximum spatial resolution and to increase the Signal to Noise Ratio of their short wavelengths. Near the centres of the study areas the gravimetric LUR model using the fast-ICA algorithm of Hyvärinen and Oja (2000) is shown to be in a complete agreement with the GPS data and the predictions of the GIA forward models, and for the whole areas, subject to epeirogeny movement of the two regions, their discrepancies reach to the extrema at -1.8 and +3.3, and -4.5 and +7.5 mm/a, respectively. We show that the largest discrepancies between the gravimetric model using the ICA method and the GIA forward model, occur for the sub-regions likely collocated with strong ice mass change signals.

Poly(hydroxyalkanoates) (PHAs) are currently considered competent candidates to replace traditional plastics in several market sectors. However, commercial PHA grades exhibit unsatisfactory smell that can negatively affect the quality of the final product. The cause of this typical rancid odour is attributed to oxidized cell membrane glycolipids, coming from Gram negative production strains, which remain frequently attached to PHAs granules after extraction. The aim of this research is the development of customised PHA nano-biocomposites for industrial applications containing organo-modified nanoclays with high adsorption properties able to capture volatile compounds responsible of the displeasing fragrance in PHAs. To this end, a methodology for the detection and identification of the key volatiles released due to oxidative degradation of PHAs has been established using a headspace solid-phase microextraction technique. We report the development of nine nano-biocomposite materials based on three types of commercial PHA matrices loaded with three species of nanoclays which represent a different polar behaviour. It has been demonstrated that although the reached outcome effect depends on the volatile nature, natural sepiolite (T2) might result in the most versatile candidate for all PHA matrices selected.

The extent of micro-phase separation in polyurethanes (PUs) depended on the molecular weight, the chemical nature and the structure of the polyol/soft segments. Balanced properties in PUs were obtained by using blends of polyols during synthesis. No previous studies have been devoted to understand the interactions between the soft segments that affect the properties of the PUs. In this study, different blends of two polyols of different nature (polyester – PE - and polycarbonate diol - CD) and similar molecular weight were prepared and their structural, thermal, surface, viscoelastic and self-adhesion properties were assessed. PE showed larger number of structural repeating units and higher number of polar groups than CD, but the carbonate-carbonate interactions in CD were stronger than the ester-ester interactions in PE. The blending of CD and PE imparted synergic structural properties, particularly in the ones containing less than 50 % PE, they were associated to the disrupt of carbonate-carbonate interactions in CD and the formation of new ester-carbonate and hydroxyl-carbonate interactions. Therefore, higher glass transition temperatures, a new diffraction peak at 2θ = 24°, one additional thermal degradation at 426-436 °C, and less steeper decline of the storage moduli to lower temperature were found in CD+PE blends with less than 50 wt.% PE. Furthermore, the different interactions between the polyol chains in the blends were also evidenced on their surface properties, and all CD+PE blends showed self-adhesion property which seemed related to the existence of ester-carbonate and carbonate-carbonate interactions.

Remotely sensed data acquired by multispectral sensors can be used to monitor soil moisture (SM) across a larger land area than in situ monitoring alone. Although there have been wide-ranging applications of remote sensing tools in SM estimation on many ecosystems, there is a limited understanding of their accuracy in restored wetlands. The objective of this study was to examine the potential of remotely sensed data from Landsat-9, Sentinel-1A SAR, and Blackswift E2 Uncrewed Aircraft Systems (UAS) in predicting SM in a restored wetland complex in the Gunnison Basin of Colorado. We tested two response variables, gravimetric SM and volumetric SM, to determine which indicator of SM was better predicted with remotely sensed data. We also tested the accuracy of remotely sensed data in predicting SM at different soil depths. Overall, satellite and UAS indices predicted gravimetric SM better than volumetric SM. The Normalized Difference Red Edge (NDRE) index from Blackswift E2 UAS had the best prediction of GSM at the depth of 0 to 5 cm (R2 = 0.86, RMSE = 7.41). Results from the study provide information on the accuracy of remotely sensed data for SM monitoring on restored wetlands.

In this study, the gravimetric characterization and analysis of the solubilized extract of the organic fraction of Urban Household Solid Waste (RSDU) from the municipality of Belém do Pará was carried out in order to obtain the composition of the collected materials and the characteristics of the liquid resulting from the solubilization of these materials . The waste used to carry out this research was collected door-to-door, in which the points and neighborhoods served were determined through the sectorization of these locations and representative statistical sampling. For the sectorization of neighborhoods, family income values ​​were considered as the main parameter. After collecting the solid waste, the material was sent to the facilities of the Federal University of Pará (FUPa), where the waste was classified into paper, cardboard, tetrapak, rigid plastic, soft plastic, metals, glass, organic matter, waste toilets, fabrics and others. The organic fraction of solid waste was separated and sent to the drying, crushing and packaging processes. Subsequently, the solubilized extract of the organic fraction of solid waste was obtained, following the methodology recommended by NBR standard nº 10.006/2004, of the Brazilian Association of Technical Standards and the values ​​obtained were compared with Ordinance GM/MS nº 888/2021 and CONAMA Resolution nº 357/2005, in addition to results obtained by other authors. After carrying out the gravimetric characterization, it was possible to obtain the average proportions of 5.09% paper, 3.20% cardboard, 0.94% tetrapak, 3.58% rigid plastic, 9.97% soft plastic, 2.00% metals, 55.57% organic matter, 1.86% glass, 14.26% sanitary waste, 3.23% fabrics and 3.00% other waste. High values ​​of organic residues were found in the gravimetric composition, which can be explained by the collection method used and the high humidity of the organic solid residues. In the analyzes of the solubilized extract, values ​​of Hp (3.69 to 4.92), Turbidity (791 to 1,733 uT), Apparent Color (8,500 to 12,500 uC), True Color (6,000 to 14,000 uC), Total Dissolved Solids (5,330 to 8,040 mg/L), Total Nitrogen (201.80 to 359.90 mg/L), Ammoniacal Nitrogen (161 to 289 mg/L), Nitrate (10 to 40 mg/L), Total Phosphorus (52.30 to 166.80 mg/L) and Chemical Oxygen Demand (28,701 mg/L to 38,608 mg/L), in addition to other measured parameters, in which such information makes it possible to check the similarities of the waste solubilization conditions to that of leachates from landfills, in addition to not being in compliance with environmental and health legislation, demonstrating risks to the local environment and public health.

This study determined the temporal variation of PM2.5 in ambient air in Thohoyandou and further assessed the associated health risks. The levels of PM2.5 were quantified for a period of 1 year (April 2017-April 2018) using the gravimetric method. There was no significant difference (P-value = 0.18) in concentrations of both PM2.5 samples collected during weekdays (11.29 µg.m-3) and weekends (9.86 µg.m-3). However, higher concentrations of PM2.5 were measured in spring and the lowest was measured in summer. The cancer risk obtained for PM2.5 (2.21 × 10−5, 3 × 10-4, and 5 × 10-4 for infants, children, and adults respectively) in the outdoor air of Thohoyandou has exceeded the limit values by the USEPA and WHO, implying a significant risk for the whole population. For non-carcinogenic risks, the HQ values were 2.60, 4.81, and 2.60 for infants, children, and adults respectively. The HQ value >1 indicates a non-carcinogenic risk to the residents in Thohoyandou and a higher risk to children. Moreover, PM2.5 in Thohoyandou is responsible for 0.15% and 0.13% of deaths resulting from cardiovascular disease and lung cancer respectively for adults above 30 years. PM2.5 is causing adverse health effects in Thohoyandou as deduced from the health risk assessment. Therefore, it is recommended that further epidemiological studies be conducted in Thohoyandou to estimate the burden of disease due to exposure to particulate matter and suitable controlling policies be arranged to reduce particulate matter.