A degradation study of polyamide 11/vermiculite nanocomposites under accelerated UV test

Accelerated photooxidation under ultraviolet (UV) test of polyamide 11 (PA11) films filled with unmodified vermiculite clay at 5 wt% was investigated up to 600 h. Film samples of ~60‐μm thick were prepared by melt compounding using a cast extruder and exposed to UV light irradiation at λ > 295 nm. Fourier transform infrared (FTIR) spectra indicated similar structural changes occurring in both PA11 and PA11/unmodified vermiculite nanoclay (UVMC) nanocomposite along the photooxidation process, resulting in imides and carboxylic acids as the main carbonyl products. It was however observed that the formation rate of carbonyls in the PA11/UVMC nanocomposite was slower than neat PA11. This behavior is consistent with the yellowing index evolution determined by ultraviolet–visible (UV–vis) spectroscopy. Further, the photooxidation stability of the samples was also evaluated by the onset oxidation temperature determined by differential scanning calorimetry. The results indicated a better stability of the nanocomposite film than neat PA11, corroborating well the data obtained by FTIR and UV–vis techniques. POLYM. ENG. SCI., 59:2449–2457, 2019. © 2019 Society of Plastics Engineers     

Preparation of chitosan‐g‐poly(acrylamide)/montmorillonite superabsorbent polymer composites: Studies on swelling,thermal, and antibacterial properties

Superabsorbent composites based on chitosan‐g‐poly(acrylamide) and montorillonite (CTS‐g‐PAAm/MMT) were synthesized through in situ radical polymerization by grafting of crosslinked acrylamide onto chitosan backbone in presence of MMT at different contents. The formation of the grafted network was confirmed by attenuated total reflectance Fourier transform infrared spectroscopy (ATR‐FTIR), thermogravimetric analysis (TGA), and differential scanning calorimetery (DSC). The obtained porous structure was observed by scanning electron microscope (SEM). The presence of clay and its interaction with chitosan‐g‐poly(acrylamide) (CTS‐g‐PAAm) matrix was evidenced by ATR‐FTIR analysis. The morphology was investigated by both X‐ray diffraction (XRD) and SEM analyses. It was suggested the formation of mostly exfoliated structures with more porous structures. Besides, the thermal stability of these composites, observed by TGA analysis, was slightly affected by the clay loading as compared to the matrix. These hydrogel composites were also hydrolyzed to achieve anionic hydrogels with ampholytic properties. Swelling behaviors were examined in doubly distilled water, 0.9 wt % NaCl solution and buffer solutions. The water absorbency of all superabsorbent composites was enhanced by adding clay, where the maximum was reached at 5 wt % of MMT. Their hydrolysis has not only greatly optimized their absorption capacity but also improved their swelling rate and salt‐resistant ability. The hydrolyzed superabsorbent showed better pH‐sensitivity than the unhydrolyzed counterparts. The results of the antibacterial activity of these superabsorbents composites against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli), assayed by the inhibitory zone tests, have showed moderate inhibition of the bacteria growth. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39747.     

Effect of cloisite 30B on the thermal and tensile behavior of poly(butylene adipate-co-terephthalate)/poly(vinyl chloride) nanoblends

Ternary PBAT/PVC/C30B nanoblends were successfully prepared via melt blending process at 130 °C and characterized by different techniques. The properties of the elaborated PBAT/PVC/C30B nanoblends were compared with those of the nonfilled PBAT/PVC blends to examine the C30B effects on the structure and properties of PBAT/PVC/C30B nanoblends. FTIR spectra revealed the presence of specific interactions between C=O of PBAT and acidic hydrogen of PVC, supporting the formation of miscible nanoblends. The PBAT/PVC/C30B morphology was investigated by both X-ray diffraction and transmission electron microscopy analyses. It was suggested the formation of mixed intercalated/partially exfoliated structures. Differential scanning calorimetry thermograms of PBAT/PVC/C30B nanoblends exhibited a single T _g and a full disappearance of the PBAT melting endotherm, confirming the complete compatibilization between PVC and PBAT. It was found that the T _g of the nanoblends were higher than those of the pristine blends due to their mixed intercalated/partially exfoliated structures. PBAT and PVC chains would be confined in a same C30B gallery causing a reduction of the chain mobility. Nanoblends showed a reduction of their thermal stability compared to their pristine blends, as a result of the catalytic effect of the C30B in the thermal degradation process. Tensile measurements displayed an improvement of mechanical properties for the ternary PBAT/PVC/C30B nanoblends relative to their virgin blends due to the insertion of clay particles into composite matrix.     

Transition metal nanoparticles doped carbon paper as a cost-effective anode in a microbial fuel cell powered by pure and mixed biocatalyst cultures

The poor wettability and high cost of the carbonaceous electrodes materials prohibited the practical applications of microbial fuel cells (MFCs) on large scale. Here, a novel nanoparticles of metal sheathed with metal oxide is electrodeposited on carbon paper (CP) to introduce as high-performance anodes of microbial fuel cell (MFC). This thin layer of metal/metal oxide significantly enhance the microbial adhesion, the wettability of the anode surface and decrease the electron transfer resistance. The investigation of the modified CP anodes in an air-cathode MFCs fed by various biocatalyst cultures shows a significant improving in the MFC performance. Where, the generated power and current density was 140% and 210% higher as compared to the pristine CP. Mixed culture of exoelectrogenic microorganism in wastewater exhibited good performance and generated higher power and current density compared to yeast as pure culture. The excellent capacitance with a distinctive nanostructure morphology of the modified-CP open an avenues for practical applications of MFCs.     

Interannual vineyard crop variability in the Castilla–La Mancha region during the period 1991–1996 with Landsat Thematic Mapper images

The vineyard crop is considered an indicator of vegetation cover processes in the Castilla–La Mancha region, as the crop has undergone far-reaching changes in the last ten years: abandonment, removal of vineyards and replacement with other crops such as cereal. The so-called ‘Change detection’ is a process that allows identification of differences in the state of the vineyard by observing it at different times. Essentially, it involves the ability to quantify temporal effects using multi-temporal datasets.

The aim of this study is to analyse the vineyard variability during the period 1991–1996 using different Landsat-5 Thematic Mapper (TM) images belonging to an identified period that highlights differences in the vegetation phenology changes. The images were firstly georeferenced and radiometrically normalized for the change detection purpose. The study area is located in central Spain and involves five councils belonging to the Castilla–La Mancha region: Mota del Cuervo, Las Mesas, Tomelloso, Socuellamos and Villarrobledo, with a surface area of 174?040?ha. This area is especially cultivated by the vineyard crop. Moreover, the study area was classified with the images acquired in 1991, using the multi-temporal masking techniques for the vineyard inventory.

The changes experimented by the vineyard have been grouped in three categories: cereal (CE), abandoned vineyard (AB) and bare soil (BS). Therefore, two methods of Normalized Difference Vegetation Index (NDVI) image difference and NDVI Change Vector Analysis (CVA) were used to map these categories of change. The results indicate that 28.4% of vineyard area undergoes changes during the period 1991–1996. The results have been checked with the ground data and all information is highly conformed.     

Interpolymer‐specific interactions and miscibility in poly(styrene‐co‐acrylic acid)/poly(styrene‐co‐N,N‐dimethylacrylamide) blends

The miscibility or complexation of poly(styrene‐co‐acrylic acid) containing 27 mol % of acrylic acid (SAA‐27) and poly(styrene‐co‐N,N‐dimethylacrylamide) containing 17 or 32 mol % of N,N‐dimethylacrylamide (SAD‐17, SAD‐32) or poly(N,N‐dimethylacrylamide) (PDMA) were investigated by different techniques. The differential scanning calorimetry (DSC) analysis showed that a single glass‐transition temperature was observed for all the mixtures prepared from tetrahydrofuran (THF) or butan‐2‐one. This is an evidence of their miscibility or complexation over the entire composition range. As the content of the basic constituent increases as within SAA‐27/SAD‐32 and SAA‐27/PDMA, higher number of specific interpolymer interactins occurred and led to the formation of interpolymer complexes in butan‐2‐one. The qualitative Fourier transform infrared (FTIR) spectroscopy study carried out for SAA‐27/SAD‐17 blends revealed that hydrogen bonding occurred between the hydroxyl groups of SAA‐27 and the carbonyl amide of SAD‐17. Quantitative analysis carried out in the 160–210°C temperature range for the SAA‐27 copolymer and its blends of different ratios using the Painter–Coleman association model led to the estimation of the equilibrium constants K₂, K_A and the enthalpies of hydrogen bond formation. These blends are miscible even at 180°C as confirmed from the negative values of the total free energy of mixing ΔG_M over the entire blend composition. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1011–1024, 2007     

Interpolymer interactions and miscibility in poly(n‐butyl methacrylate‐co‐methacrylic acid)/poly(styrene‐co‐N,N‐dimethyl acrylamide) blends

The miscibility of poly(n‐butyl methacrylate‐co‐methacrylic acid) containing 18 mol % methacrylic acid (BMAM‐18) and poly(styrene‐co‐N,N‐dimethyl acrylamide) containing 17 mol % N,N‐dimethyl acrylamide (SAD‐17) was investigated with viscometry, differential scanning calorimetry (DSC), and Fourier transform infrared (FTIR) spectroscopy. The DSC analysis showed a single glass‐transition temperature for all the blends, indicating that these copolymers were miscible over the entire composition range. The glass‐transition temperatures of these blends were higher than those calculated with the additivity rule. This was characteristic of the presence of specific interactions. The interactions between BMAM‐18 and the tertiary amide of SAD‐17 were studied with FTIR spectroscopy, which revealed that hydrogen‐bonding interactions occurred between the hydroxyl groups of BMAM‐18 and the carbonyl amide of SAD‐17. A new band characterizing these interactions appeared around 1613 cm^?1. The quantitative results showed that the fraction of the associated amide increased with an increase in the amount of the acidic BMAM‐18 copolymer. Although BMAM‐18 and SAD‐17 led to homogeneous solutions in butan‐2‐one, as the concentration of N,N‐dimethyl acrylamide increased to 32 mol % [as within the poly(styrene‐co‐N,N‐dimethyl acrylamide) containing 32 mol % N,N‐dimethyl acrylamide], complexation occurred when this latter compound was mixed with BMAM‐18 in butan‐2‐one. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 2717–2724, 2006     

Enhanced collective detection for GNSS weak signals acquisition in Rayleigh channel

Global navigation satellite system applications based on high sensitivity and weak‐signal acquisition is a difficult task and has become an important research area. Algorithms and techniques are proposed, principally those associated to cases of limited global navigation satellite system signal availability. Collective detection is a new technique that seems to offer better solutions in a such situation. This paper presents a performance analysis of GPS L₁ noncoherent acquisition via collective detection based on the systematic and efficient collective acquisition algorithm in the Rayleigh fading channel, firstly in the case of a fixed threshold detection and secondly in the case of adaptive threshold detection based on a constant false alarm rate. To compare these methods with traditional acquisition schemes, we develop detection and false alarm probability analytic expressions.     

Effective MgO‐doped TiO2 nanoaerogel coating for crystalline silicon solar cells improvement

This study looks at investigating the influence of high surface area TiO₂ and MgO‐doped TiO₂ aerogel nanomaterials to improve the photovoltaic performance of monocrystalline silicon (mono‐Si) solar cells. TiO₂ and MgO‐doped TiO₂ anatase nanoaerogels were synthesized via a single‐step colloidal homogeneous precipitation sol‐gel method in a compact high‐pressure hydrogen reactor. TiO₂‐based nanoparticles were encapsulated in ethylene vinyl acetate resins, and the obtained composite solutions were screen printed on the textured surface of the cells. The specific surface area, microstructural, composition, and optical properties of the nanoaerogels were characterized by Brunaur‐Emmett‐Teller, X‐ray powder diffractometer, energy‐dispersive X‐ray spectroscopy, field emission transmission electron microscope, field emission scanning electron microscope, and ultraviolet‐visible spectrophotometry. We observed that the MgO‐doped TiO₂ (2% mol) nanoaerogel exhibited a much superior specific surface area (231 m²/g) compared with the undoped TiO₂ (154 m²/g). Experimental results showed that the calculated relative power conversion efficiency increased by 4.6% for the MgO‐doped TiO₂ coating and 3.4% for the undoped TiO₂ under a simulated one‐sun illumination.