Low Dispersion Research Articles

Divergent lineages in a young species: The case of datilillo (Yucca valida), a broadly distributed plant from the Baja California Peninsula.

Globally, barriers triggered by climatic changes have caused habitat fragmentation and population allopatric divergence. Across North America, oscillations during the Quaternary have played important roles in the distribution of wildlife. Notably, diverse plant species from the Baja California Peninsula in western North America, isolated during the Pleistocene glacial-interglacial cycles, exhibit strong genetic structure and highly concordant divergent lineages across their ranges. A representative plant genus of the peninsula is Yucca, with Y. valida having the widest range. Although a dominant species, it has an extensive distribution discontinuity between 26° N and 27° N, suggesting restricted gene flow. Moreover, historical distribution models indicate the absence of an area with suitable conditions for the species during the Last Interglacial, making it an interesting model for studying genetic divergence. We assembled 4411 SNPs from 147 plants of Y. valida throughout its range to examine its phylogeography to identify the number of genetic lineages, quantify their genetic differentiation, reconstruct their demographic history and estimate the age of the species. Three allopatric lineages were identified based on the SNPs. Our analyses support that genetic drift is the driver of genetic differentiation among these lineages. We estimated an age of less than 1 million years for the common ancestor of Y. valida and its sister species. Habitat fragmentation caused by climatic changes, low dispersal, and an extensive geographical range gap acted as cumulative mechanisms leading to allopatric divergence in Y. valida.

Highly Selective O-Phenylene Bisurea Catalysts for ROP: Stabilization of Oxyanion Transition State by a Semiflexible Hydrogen Bond Pocket.

Organocatalyzed ring-opening polymerization (ROP) is a versatile technique for synthesizing biodegradable polymers, including polyesters and polycarbonates. We introduce o-phenylene bisurea (OPBU) (di)anions as a novel class of organocatalysts that are fast, easily tunable, mildly basic, and exceptionally selective. These catalysts surpass previous generations, such as thiourea, urea, and TBD, in selectivity (kp/ktr) by 8 to 120 times. OPBU catalysts facilitate the ROP of various monomers, achieving high conversions (>95%) in seconds to minutes, producing polymers with precise molecular weights and very low dispersities (Đ ≈ 1.01). This performance nearly matches the ideal distribution expected from living polymerization (Poisson distribution). Density functional theory (DFT) calculations reveal that the catalysts stabilize the oxyanion transition state via a hydrogen bond pocket similar to the "oxyanion hole" in enzymatic catalysis. Both experimental and theoretical analyses highlight the critical role of the semirigid o-phenylene linker in creating a hydrogen bond pocket that is tight yet flexible enough to accommodate the oxyanion transition state effectively. These new insights have provided a new class of organic catalysts whose accessibility, moderate basicity, excellent solubility, and unparalleled selectivity and tunability open up new opportunities for controlled polymer synthesis.

Photochemical [2 + 2] Cycloaddition Enables the Synthesis of Highly Thermally Stable and Acid/Base-Resistant Polyesters from a Nonpolymerizable α,β-Conjugated Valerolactone.

We report a simple strategy to transform a nonpolymerizable six-membered α,β-conjugated lactone, 5,6-dihydro-2H-pyran-2-one (DPO), into polymerizable bicyclic lactones via photochemical [2 + 2] cycloaddition. Two bicyclic lactones, M1 and M2, were obtained by the photochemical [2 + 2] cycloaddition of tetramethylethylene and DPO. Ring-opening polymerization (ROP) of M1 and M2 catalyzed by diphenyl phosphate (DPP), La[N(SiMe3)2]3, and 1-tert-butyl-4,4,4-tris(dimethylamino)-2,2-bis[tris (dimethylamino) phosphoranylide-namino]-2λ5, 4λ5-catenadi(phosphazene) (tBu-P4) were conducted. M1 is highly polymerizable, either DPP or La[N(SiMe3)2]3 could catalyze its living ROP under mild conditions, affording the well-defined PM1 with a predictable molar mass and low dispersity. M2 could only be polymerized with tBu-P4 as the catalyst, also generating the same polymer PM1. PM1 has high thermal stability, with a Td,5% being up to 376 °C. Ring-opening copolymerization (ROcP) of M1 and δ-valerolactone (δ-VL) catalyzed by La[N(SiMe3)2]3 afforded a series of random copolymers with enhanced thermal stabilities. Both PM1 and the copolymer containing 10 mol % M1 exhibited excellent resistance to acidic and basic hydrolysis. Our results demonstrate that direct photochemical [2 + 2] cycloaddition of α,β-conjugated valerolactone is not only a strategy to tune its polymerizability, but also allows for the synthesis of highly thermally stable aliphatic polyesters, inaccessible by other methods.

Study on Mechanical and Electrical Properties of High Content CNTs/Cu Composites.

It is expected that composites made of carbon nanotubes (CNT) and copper (Cu) display both mechanical and electrical properties, but the low damage dispersion and high-quality composite of high-content CNTs have always been research difficulties. In this paper, high-content CNTs/Cu composites were prepared. The effects of the sintering method, sintering temperature, directional rolling and the CNTs' content on the relative density, hardness and electrical conductivity of the composites were studied. The uniform dispersion of high-content CNTs in Cu matrix was achieved by ball milling, sintering and rolling, and the processes did not cause more damage to the CNTs. The properties of composites prepared by spark plasma sintering (SPS) and vacuum hot pressing sintering (HPS) were compared, and the optimum process parameters of SPS were determined. When the CNTs' content is 2 wt.%, the hardness is 134.9 HBW, which is still 2.3 times that of pure Cu, and the conductivity is the highest, reaching 78.4%IACS. This study provides an important reference for the high-quality preparation and performance evaluation of high-content CNTs/Cu composites.

Multi-stage evolution of the monzonitic Larvik Plutonic Complex (Oslo Rift, Norway) and its implications for the formation of the Kodal Fe-Ti-P(−REE) deposit

The Larvik Plutonic Complex is a monzonitic complex that was emplaced early during the formation of the Permian Oslo Rift (southern Norway). It extends across its entire width (around 50 km), and is made up of a majority of larvikite (augite monzonite) and lardalite (nepheline monzogabbro to nepheline syenite) distributed in ten successive intrusive units that partially intersect each other. The Larvik Plutonic Complex also hosts occurrences of singular Fe-Ti-P-rich rocks of magmatic origin, including the Kodal deposit. These are mainly composed of titanomagnetite, ilmenite, titanaugite and apatite, the latter also featuring rare earth elements (REE) enrichment. Here, we aim to unravel the conditions that allowed the Kodal deposit to form, and determine why other mineralized bodies are not seen elsewhere in the Larvik Plutonic Complex. We compared the petrography and elemental and isotope (Sr, Nd and Hf) geochemistry of both the Kodal mineralization and the neighboring larvikite, in order to provide evidence of their petrogenetic relationship. Both lithologies share the same isotopic ratios (87Sr/86Sr(i): 0.7035–0.7043; εNd(i): +2.37 − +3.48; εHf(i): +3.39 − +9.16), which would suggest a single homogeneous source. The very low dispersion of our isotopic data also suggests that crustal contamination levels in the area were low to negligible. Normalized trace diagrams of larvikite in several localities of the Larvik Plutonic Complex also show enrichments in most incompatible elements, which becomes more prevalent towards the Kodal deposit. Elements like Sr and Eu(2+) follow an opposite trend, because of their compatibility in plagioclase. We therefore infer that the region around the Kodal deposit hosts more fractionated larvikite due to the previous crystallization of successive plagioclase cumulates. We deduce that the Kodal lobe corresponds to a more evolved intrusion, which is no part of Pluton V per se, as considered in the literature until now, but instead derives at least from a monzonitic magma at the origin of the plutons V to VIII). This also implies that the formation of Fe-Ti-P mineralization at Kodal was most likely a consequence of enrichment of the residual melt in alkaline elements and incompatible elements. These conditions support an early hypothesis of formation by silicate-liquid immiscibility, along with petrographic evidence of disequilibrium at the mineralogical scale. However, further analyses would be required to test the hypotheses of silicate-liquid immiscibility against an accumulation of the Fe-Ti-P mineralization from an evolved intermediate magma.

Structural changes and grading mechanism of lignin during solid alkali-active oxygen extraction and grading

Cooking with active oxygen and solid alkali (CAOSA) is an efficient pretreatment method for biomass. For better grading of the lignin yellow liquor, the different lignin fractions and the recovered solid alkali were obtained using a simultaneous acid-alkali graded separation method. The results indicated that the recovery rate of solid alkali was 67.25 %, and the grading of lignin components was characterized by smaller dispersion coefficients, and more stable properties and structure. Lignin fractions with low dispersion coefficients possess more key structures, including the Phenol hydroxyl group (ArOH), Methoxy (OMe), and β-aryl ether (β-O-4), and have better thermal properties. The low molecular weight L4 has the highest ArOH content (2.1 mmol/g), which provides better antioxidant properties. The CAOSA process destroyed the S-unit and prevented lignin from condensation. Furthermore, the CAOSA process protected carbohydrates, which could effectively prevent them from dehydrating and re-polymerizing into pseudo-lignin. This allowed the pulp to remain natural, which was beneficial for subsequent transformation and utilization. Overall, the efficient separation of biomass components and lignin grading method proposed by combining the CAOSA process with the acid-alkali grading separation method has a strong application prospect and provides a theoretical basis for the high-value utilization of biomass and lignin.

A Review of Whey Protein-Based Bioactive Delivery Systems: Design, Fabrication, and Application.

The efficacy of many edible bioactive agents is limited by their low water dispersibility and chemical instability in foods, as well as by their poor bioaccessibility, low absorption, and metabolism within the human gastrointestinal tract. Whey proteins are amphiphilic molecules that can be used to construct a variety of edible carrier systems that can improve the performance of bioactive ingredients. These carrier systems are being used by the food and biomedical industries to encapsulate, protect, and deliver a variety of bioactive agents. In this article, we begin by providing an overview of the molecular and functional characteristics of whey proteins, and then discuss their interactions with various kinds of bioactive agents. The ability of whey proteins to be used as building blocks to assemble different kinds of carrier systems is then discussed, including nanoparticles, hydrogels, oleogels, bigels, nanofibers, nanotubes, and nanoemulsions. Moreover, applications of these carrier systems are highlighted. Different kinds of whey protein-based carriers can be used to encapsulate, protect, and deliver bioactive agents. Each kind of carrier has its own characteristics, which make them suitable for different application needs in foods and other products. Previous studies suggest that whey protein-based carriers are particularly suitable for protecting chemically labile bioactive agents and for prolonging their release profiles. In the future, it is likely that the applications of whey protein-based carriers in the food and pharmaceutical fields will expand.

Detailed chemical abundances of the globular cluster Terzan 6 in the inner bulge

We used near-infrared spectroscopy at medium-high resolution (R = 8000 − 25 000) to perform the first comprehensive chemical study of the intermediate luminosity bulge globular cluster Terzan 6. We derived detailed abundances and abundance patterns of 27 giant stars, likely members of Terzan 6, based on their accurate Hubble Space Telescope proper motions and line-of-sight radial velocities. From the spectral analysis of these stars, we determined an average heliocentric radial velocity of 143.3 ± 1.0 km s−1 with a velocity dispersion of 5.1 ± 0.7 km s−1 and an average [Fe/H] = −0.65 ± 0.01 and a low 1σ dispersion of 0.03 dex. We also measured some depletion of [Mn/Fe] with respect to the solar-scaled values and enhancement of for [Ca/Fe], [Si/Fe], [Mg/Fe], [Ti/Fe], [O/Fe], [Al/Fe], [Na/Fe], and, to a lower extent, for [K/Fe], consistent with previous measurements of other bulge globular clusters and favoring the scenario of a rapid bulge formation and chemical enrichment. Some spread in the light element abundances suggest the presence of first- and second-generation stars, typical of genuine globulars. Finally, we measured some depletion of carbon and low 12C/13C isotopic ratios, as in previous studies of field and cluster bulge giants, indicating that extra-mixing mechanisms should be at work during the post main sequence evolution in the high metallicity regime as well.

Host Galaxies for Four Nearby CHIME/FRB Sources and the Local Universe FRB Host Galaxy Population

We present the host galaxies of four apparently nonrepeating fast radio bursts (FRBs), FRB 20181223C, FRB 20190418A, FRB 20191220A, and FRB 20190425A, reported in the first Canadian Hydrogen Intensity Mapping Experiment (CHIME/FRB) catalog. Our selection of these FRBs is based on a planned hypothesis testing framework where we search all CHIME/FRB Catalog-1 events that have low extragalactic dispersion measure (<100 pc cm−3), with high Galactic latitude (∣b∣ > 10°) and saved baseband data. We associate the selected FRBs with galaxies with moderate to high star formation rates located at redshifts between 0.027 and 0.071. We also search for possible multimessenger counterparts, including persistent compact radio and gravitational-wave sources, and find none. Utilizing the four FRB hosts from this study, along with the hosts of 14 published local Universe FRBs (z < 0.1) with robust host association, we conduct an FRB host demographics analysis. We find all 18 local Universe FRB hosts in our sample to be spirals (or late-type galaxies), including the host of FRB 20220509G, which was previously reported to be elliptical. Using this observation, we scrutinize proposed FRB source formation channels and argue that core-collapse supernovae are likely the dominant channel to form FRB sources. Moreover, we infer no significant difference in the host properties of repeating and apparently nonrepeating FRBs in our local Universe FRB host sample. Finally, we find the burst rates of these four apparently nonrepeating FRBs to be consistent with those of the sample of localized repeating FRBs observed by CHIME/FRB. Therefore, we encourage further monitoring of these FRBs with more sensitive radio telescopes.

2‐Azetine Derivatives as a Class of New Monomers for Controlled Ring‐Opening Metathesis Polymerization towards Polyenamides†

Comprehensive SummaryNitrogen‐containing polymers have found a wide myriad of applications in materials science and other different areas, and have attracted much attention towards the development of new synthetic methods. Ring‐opening metathesis polymerization represents an area of great versatility and potential for the synthesis of highly functionalized polymers with low dispersity and control over molecular weight and architecture complexity. Expanding the scope of monomers through the incorporation of nitrogen atoms would further expand their utilities. In this work, a controlled synthesis of polymers with in‐chain enamide moiety through ring‐opening metathesis polymerization was developed by utilizing azetine derivatives as the monomers. Relatively short synthetic routes were designed and generated a panel of five monomers. The polymerization exhibited living characteristics, as linear relationship between molecular weights and degrees of polymerization and relatively narrow molar mass distributions were observed, which was further confirmed by successful diblock copolymers formation through sequential addition of two monomers. The resulting polymers that contain the enamide moiety within the backbone exhibited good stability and underwent facile degradation under acidic conditions.

Two distinct molecular cloud populations detected in massive galaxies

ABSTRACT We present new ALMA observations of CO, CN, CS, HCN, and HCO$^{+}$ absorption seen against the bright and compact radio continuum sources of eight galaxies. Combined with archival observations, they reveal two distinct populations of molecular clouds, which we identify by combining CO emission and absorption profiles to unambiguously reveal each cloud’s direction of motion and likely location. In galaxy discs, we see clouds with low velocity dispersions, low line-of-sight velocities, and a lack of any systemic inflow or outflow. In galactic cores, we find high velocity dispersion clouds inflowing at up to 550 km s−1. This provides observational evidence in favour of cold accretion on to galactic centres, which likely contributes to the fuelling of active galactic nuclei. We also see a wide range in the CO(2-1)/CO(1-0) ratios of the absorption lines. This is likely the combined effect of hierarchical substructure within the molecular clouds and continuum sources which vary in size with frequency.

Al nanowire-embedded silicon for broadband optical modulation: Forming mechanism and optical performance

In recent decades, silicon has been widely used in light regulation devices, owing to its wideband high refractive index and low dispersion. To meet the increasing demands for various applications, optical modulation techniques appear of great potential to enhance the optical performance of Si-based devices. However, challenges still remain in achieving precise control over the band structure and resonance modes without introducing complex artificial structures. In this study, a composite film composed of silicon embedded with high fraction aluminum nanowires was developed by magnetron sputtering. It was revealed that the formation of aluminum nanowires was attributed to the spontaneous phase separation between silicon and aluminum, which was strongly dependent on the filling fraction and surface diffusion length of the aluminum during the co-sputtering process. The composite microstructure was precisely regulated by manipulating adatom diffusion and reevaporation through ion bombardment, thereby modifying its broadband optical properties. Moreover, exceptional electromagnetic properties were achieved by incorporating aluminum nanowires into silicon, as evidenced by the metallic behaviors in the short-wavelength regime and dielectric properties in the infrared spectrum range.

Encapsulation and controlled delivery of curcumin by self-assembled cyclodextrin succinate/chitosan nanoparticles

Low aqueous dispersibility and poor stability severely restrict the bioaccessibility of curcumin in health-related products. Constructing highly effective delivery carriers is essential to overcome the limitation. In this study, a novel and simple self-assembly process driven by electrostatic interaction was developed to prepare cyclodextrin succinate/chitosan (SACD/CS) nanoparticles. Spherical SACD/CS nanoparticles were obtained by adjusting the ratio of SACD:CS to obtain an average size and ζ-potential of around 500 nm and 20 mV, respectively. By analyzing the intermolecular interactions and crystalline structure of SACD/CS nanoparticles, it is indicated that SACD could act as crosslinking nodes, and contributed to transformation of molecular arrangement in the nanoparticles. The noncytotoxic SACD/CS nanoparticles were further used as curcumin carriers and showed significant improvement on curcumin stability, with the retention index of curcumin under physiological conditions increased from 19% to 62%. Moreover, the Cur-SACD/CS nanoparticles displayed controlled release behavior of curcumin during in vitro digestion, with 9%, 22%, and 44% of curcumin released at the end of the oral, stomach, and small intestine stage, respectively. This study developed a novel and effective strategy for oral delivery of curcumin, showing promising potential for improving the bioaccessibility and bioavailability of bioactive compounds like curcumin.

A double sampling multivariate GLR control charting method for joint monitoring of process mean vector and covariance matrix under additive covariate model

A process is in its stable state when it has sufficient precision and accuracy. The accuracy is expressed as the deviation of the process mean from its target while the low dispersion indicates the high process precision. Therefore, joint monitoring of multivariate process mean and variability ensures a high rate of producing items. This study proposes a multivariate generalized likelihood ratio scheme called DS-MGLR with two features: (1) considering the effect of imprecise observations, and (2) enhancing the chart sensitivity in reacting to process disturbances. Since the shift magnitude in the distribution parameters is not known in advance, the expected average run length is also calculated for both the MGLR and DS-MGLR charts. To reduce the impact of measurement errors, an improved version of the DS-MGLR chart based on multiple measurement approach is developed. Three comparative studies are presented to indicate the importance of the properties of the developed charts. The first study confirms the efficiency of the double sampling strategy, while the second study indicates the error effect. The third one shows the effectiveness of the multiple measurement approach in compensating for the error contamination. Finally, the applicability of the proposed chart is highlighted using a real data example.

Design and Performance Analysis of Compact Printed Ridge Gap Waveguide Phase Shifters for Millimeter-Wave Systems.

This paper introduces compact Printed Ridge Gap Waveguide (PRGW) phase shifters tailored for millimeter-wave applications, with a focus on achieving wide operating bandwidth, and improved matching and phase balance compared to single-layer technology. This study proposes a unique approach to achieve the required phase shift in PRGW technology, which has not been previously explored. This study also introduces a novel analytical approach to calculate the cutoff frequency and propagation constant of the PRGW structure, a method not previously addressed. Furthermore, the utilization of multi-layer PRGW technology enables the realization of multi-layer beamforming networks without crossing, thereby supporting wideband operation in a compact size. The proposed design procedure enables the realization of various phase shift values ranging from 0∘ to 135∘ over a broad frequency bandwidth centered at 30 GHz. A 45-degree phase shifter is fabricated and tested, demonstrating a 10 GHz bandwidth (approximately 33% fractional bandwidth) from 25 GHz to 35 GHz. Throughout the operating bandwidth, the phase balance remains within 45 ± 5∘, with a deep matching level of -20 dB. The proposed phase shifter exhibits desirable characteristics, such as compactness, low loss, and low dispersion, making it a suitable choice for millimeter-wave applications, including beyond 5G (B5G) and 6G wireless communications.

About Polycondensation, Disproportionation, and Cyclization of Acetylated Poly(L‐Lactide) Esters

AbstractL‐lactide (LA) is polymerized with ethyl L‐lactate or trifluoroethanol as initiators (LA/In = 30/1), and the resulting poly(L‐lactide) esters are acetylated with acetic anhydride. The acetylated PLA esters are mixed with SnOct2, dibutyltin bis(4‐chlorophenoxide), or dibutyltin bis(pentafluorophenoxide) in solution and crystallized at 120 °C. The doped crystals are annealed at 140 °C or at 160 °C for 7, 14, and 28 days, and the chemical modifications that occurred in the solid state are monitored by matrix‐assisted laser desorption/ionization time‐of‐flight (MALDI TOF) mass spectrometry, gel permeation chromatography (GPC), and differential scanning calorimetry (DSC) measurements. All catalysts promoted polycondensation, while no significant formation of cycles is observed. However, in the presence of SnOct2, disproportionation of chains occurred upon annealing at 120 or 140 °C, and crystallites consisting of extended chains with Mn values ≈3500 – 3600 and low dispersities (Ð &lt; 1.5) are formed.

A morphogenetic characterisation of a potentially dominant African marine species in Europe

Studying the early stages of the introduction of non-indigenous species (NIS) is crucial as it allows immediate management actions aimed at preventing NIS spread at a time when these actions are more likely to be effective. Recent species introductions present unique opportunities to study key aspects of the invasion process. However, comprehensive information on how and when NIS are first introduced remains rare. We assessed the characteristics of the introduction of a member of the widespread Pyura stolonifera species group (Chordata, Tunicata) in Europe. These ascidians are important bioengineer species that can attain amongst the highest benthic biomass per surface area ever reported. We collected introduced individuals on the coast of the northwestern Iberian Peninsula, an area with high shipping traffic and one of the world’s most important mussel farming regions. The specimens were analysed using taxonomic and genetic tools. Both field surveys and taxonomic analysis showed that one of the African members of the species group, Pyura herdmani, has recently been introduced to Europe and, although it does not yet form the large aggregates found in the native range, it is already well-established. Genetic data revealed that only the northwest African lineage of P. herdmani has been introduced to Europe. Considering the low dispersal capabilities of the early life-history stages of P. herdmani, the introduction of this species into Europe can only be explained via human mediated transport of NIS. In order to prevent any detrimental effects on both native biota and/or economically-important anthropogenic activities, regular monitoring of recent NIS introductions is urgently required.

Enhancing the efficacy of fluconazole against Leishmania major: Formulation and evaluation of FLZ-nanoemulsions for topical delivery

BackgroundCutaneous Leishmaniasis (CL) remains a significant public health concern, particularly in the tropical and subtropical regions. Present treatment options for CL such as Fluconazole (FLZ) face limitations, including low solubility and bioavailability. This study aimed to address these challenges by investigating the use of nano-emulsions (NEs) to enhance the efficacy of FLZ against Leishmania major(L.major). Materials and methodsFLZ-NEs were formulated with oleic acid, Tween-20, and ethanol using low-energy emulsification at various surfactant/co-surfactant ratios. Subsequently, a comprehensive analysis was conducted to assess the physicochemical characteristics of the samples. This analysis encompassed stability, zeta potential, pH, viscosity, refractive index, and droplet size. We then studied the anti-parasitic properties of these optimized FLZ-NEs both in vitro and in vivo. ResultsThe selected nano-emulsion (NE) formulation (2 % oleic acid, 20 % Tween 20, 10 % ethyl alcohol) showcased desirable properties like small droplet size (10.51 ± 0.24 nm), low dispersity (0.19 ± 0.03), and zeta potential value (- 0.41 ± 0.17 mV), key for stability and targeted drug delivery. This optimal formulation translated into remarkable efficacy. In vitro, FLZ-NEs demonstrated a threefold increase in their ability to combat promastigotes and a remarkable thirtyfold increase in their ability to combat amastigotes. Additionally, they demonstrated a ninefold advantage in their ability to specifically target parasites within infected macrophages, thereby attacking the infection site. These promising in vitro results translated into improved outcomes in vivo. Compared to other chemicals studied, FLZ-NE-treated mice showed decreased disease severity, weight growth, and quicker ulcer healing. It was further supported by histopathological research, which showed reduced tissue damage linked to Leishmania infection. ConclusionThese findings show the potential of nanotechnology-based drug delivery in improving anti-leishmanial treatment.

Social media marketing strategies: an empirical study in the hotel sector

The objective of this study is to analyze the use of the social network Facebook by clients of the Hotel RZR, located in the city of Cúcuta, Colombia. The study is quantitative, follows a cross-sectional design and the questionnaire was applied to a sample of 102 hotel guests. The descriptive statistics reflect a standard deviation of 0.579, which indicates that there is a low dispersion of the data with respect to the average value. The results show that age, the level of study and gender are aspects related to customers' preferences in the use of Facebook. It is concluded that Facebook's social network has become a valuable digital marketing tool and the RZR Hotel must innovate in the network, to boost communication with customers and exploit other benefits offered by Facebook, such as segmentation, branding, online reputation and traffic generation.

Bio-based non-isocyanate poly(urea)-PEG hybrids for VOC-free waterborne dispersions and fast UV-curable film application

Poly(urethane)-acrylate hybrids are often used to yield high-performing fast UV-curable coatings thanks to their highly reactive acrylate moieties. However, they are usually manufactured from toxic and petro-based isocyanate (e.g. isophorone diisocyanate, hexamethylene diisocyanate) monomers and are dispersed in water using toxic volatile neutralization agent (e.g. triethylamine). To tackle those issues, hydrophobic and bio-based non-isocyanate poly(urea) (NIPUrea) blocks have been synthesized and coupled with hydrophilic poly(ethylene glycol) diacrylate (PEGdA) via aza-Michael reaction to yield VOC-free non-ionic waterborne NIPUrea-acrylate dispersions. Those amphiphilic NIPUrea-PEG hybrids enabled the development of low particle-size waterborne dispersions for fast UV curable films (curing time < 1 min) with high gel content (>98 %) and tunable mechanical properties.