High Molecular Weight Research Articles

Functional and physicochemical characterization of marine exopolysaccharide derived from the novel bacterium Algoriphagus sp. K5R and its application towards biomineralization of gold and silver

AbstractThe widespread use of synthetic polymers in various industries has raised worldwide concerns regarding their ecological impact and effects on human health. As a result, biopolymers have emerged as a promising alternative. Among them, exopolysaccharides (EPSs) produced by microbes from terrestrial niches have been extensively studied. However, recent reports have indicated that microbes from marine environments can also produce unique EPSs that could serve as sustainable substitutes to meet the escalating demand for biopolymers. The present study, for the first time, reports EPS production from novel marine bacterium Algoriphagus sp. K5R for sustainable application development. Interestingly, physicochemical analyses suggest that EPS K5R is a high molecular weight (1190.63 kDa) heteropolysaccharide composed of galacturonic acid, glucose and mannose. To evaluate EPS production, growth and fermentation kinetics were performed, which revealed that it was a primary metabolite having a maximum production of 4.79 ± 0.57 g L−1 with 2% (w/v) glucose. Moreover, EPS K5R exhibits exceptional functional properties, namely high water‐holding capacity (720% ± 80.29%) and oil‐holding capacity (493.33% ± 49.74% for coconut oil and 533.32% ± 17.47% for olive oil), and non‐Newtonian pseudo‐plastic behavior which render it a promising candidate for application in the cosmetics and food industries. In fact, its anti‐oxidant capabilities make it an ideal biological reducing agent for metal nanoparticle synthesis. Overall, this study highlights the potential of marine EPSs for a diverse array of industrial applications. © 2024 Society of Chemical Industry.

Effects of mineral adsorption on the molecular composition of soil dissolved organic matter: Evidence from spectral analyses

The adsorption of soil dissolved organic matter (DOM) by minerals is crucial for long-term carbon storage and has been extensively studied. However, the variations in soil DOM composition resulting from adsorption by different minerals have rarely been investigated from a spectral perspective. This study examined the impact of non‑iron (kaolinite) and iron-bearing (ferrihydrite) minerals on the concentration and characteristics of DOM from dark brown soil during a 60-h-long incubation experiment. Soil dissolved organic carbon was removed more efficiently by ferrihydrite (66.2 %) than by kaolinite (14.8 %). UV–Vis spectroscopic analysis indicated that DOM with high aromaticity and molecular weight exhibited a strong affinity for both ferrihydrite and kaolinite. The fluorescence of soil DOM decreased in the ferrihydrite treatment, with a notable reduction in humic-like fluorescent components identified through fluorescent excitation-emission matrix coupled parallel factor analysis. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy revealed that carboxyl groups were critical in DOM adsorption on ferrihydrite, participating in ligand exchange, hydrogen bonding, and electrostatic attraction. This study highlights the important role of iron-bearing minerals in soil carbon sequestration and demonstrates how different mineral alter soil DOM composition, potentially influencing the cycling of organic carbon in terrestrial systems.

Bimolecular Sandwich Aggregates of Porphyrin Nanorings.

Extended π-systems often form supramolecular aggregates, drastically changing their optical and electronic properties. However, aggregation processes can be difficult to characterize or predict. Here, we show that butadiyne-linked 8- and 12-porphyrin nanorings form stable and well-defined bimolecular aggregates with remarkably sharp NMR spectra, despite their dynamic structures and high molecular weights (12.7 to 26.0 kDa). Pyridine breaks up the aggregates into their constituent rings, which are in slow exchange with the aggregates on the NMR time scale. All the aggregates have the same general two-layer sandwich structure, as deduced from NMR spectroscopy experiments, including 1H DOSY, 1H-1H COSY, TOCSY, NOESY, and 1H-13C HSQC. This structure was confirmed by analysis of residual dipolar couplings from 13C-coupled 1H-13C HSQC experiments on one of the 12-ring aggregates. Variable-temperature NMR spectroscopy revealed an internal ring-on-ring rotation process by which two π-π stacked conformers interconvert via a staggered conformation. A slower dynamic process, involving rotation of individual porphyrin units, was also detected by exchange spectroscopy in the 8-ring aggregates, implying partial disaggregation and reassociation. Molecular dynamics simulations indicate that the 8-ring aggregates are bowl-shaped and highly fluxional, compared to the 12-ring aggregates, which are cylindrical. This work demonstrates that large π-systems can form surprisingly well-defined aggregates and may inspire the design of other noncovalent assemblies.

Insights on influence of polymer molecular weight on gas sorption, transport and plasticization in glassy 6FDA-DAM polyimide membranes

It is well-known that spinning of defect-free asymmetric polyimide hollow fibers is promoted by using high polymer molecular weight. On the other hand, effects of polymer molecular weight on microstructure and separation performance of dense film 6FDA-based polyimide membranes relevant to sheath layers of composite membranes are less well-explored. In this work, gas sorption, diffusion and permeation of CO2, N2 and CH4 for 6FDA-DAM dense films are considered for 45 kDa and 176 kDa weight average molecular weights. Such molecular weights are relevant for practical hollow fiber spinning of membranes. Earlier results for polystyrene samples show similar trends in dual mode sorption model results like those noted here for the 6FDA-DAM polyimide case; however, effects on permeation like those considered here were not addressed for the polystyrene case. Here we also address actual pure and mixed gas CO2 and CH4 permeation and show higher free volumes, higher gas permeability but lower 50:50 CO2/CH4 selectivity associated with the higher molecular weight sample. Analysis using the self-consistent dual-mode sorption and transport models help understand the observed trends. Our results suggest denser packing of polymer segments exists in the Henry's law environment of the low molecular weight sample. Moreover, the higher polymer segmental packing in the Henry's law environment suppresses CO2 plasticization with a dual-mode microstructure controlling separation performance and plasticization behavior for this important member of the 6FDA polyimide family. We show evidence of effects of charge transfer complexes as possible main features in these trends. These dense film results help guide future work on dense sheath layers on composite hollow fiber membranes.

A quantitative comparison of economic viability, volatile organic compounds, and particle-bound carbon emissions from a diesel engine fueled with biodiesel blends

Despite the environmental advantages of biofuel blends, detailed studies on emissions of polycyclic aromatic hydrocarbons (PAHs), n-alkanes, and particle-bound carbon from diesel engines, particularly when fueled with biodiesel, remain limited. This study addresses these gaps by analyzing biodiesel blends from neem, linseed, and jatropha oils produced via mechanical extraction and assessing their impact on volatile organic compounds and particle-bound carbon emissions in diesel engine. Economic evaluations of production costs, engine modifications, and payback periods are also conducted. The result shows that jatropha biodiesel exhibits a calorific value of 35.7 MJ/kg, while neem biodiesel shows superior oxidative stability due to its low iodine value. Additionally, linseed biodiesel displays favorable cold flow properties due to its high density and cetane value. Compared to D100, the N10 and N30 blend notably reduced high molecular weight PAH emissions by 10.7 % and 38.4 %, respectively, with the N30 blend achieving a remarkable 76 % reduction in formaldehyde emissions. Conversely, the J10 blend increased specific PAHs, while the J30 blend reduced PAHs by 21.3 %. Both L10 and L30 blends showed reduced naphthalene emissions, with the J30 blend notably reducing elemental carbon (EC) by 31.4 %, although organic carbon (OC) slightly increased. In contrast, the N30 blend decreased both EC and OC emissions, demonstrating a dose-dependent relationship between biodiesel concentration and emissions reduction. Overall, Jatropha biodiesel blends offer the best balance of economic efficiency and emission reductions, resulting in shorter payback periods and lower carcinogenic risks. Neem and linseed blends also provide environmental benefits but with varying economic implications, highlighting the trade-offs between production costs and long-term sustainability.

A membrane fouling control strategy based on a combination of pre-treatment mitigation and in-situ membrane surface regulation using a composite coagulant

Ultrafiltration technology (UF) is efficient in surface water treatment, but its development and widespread application are limited by membrane fouling. Herein, an efficient and stable polymerized ferric titanium coagulant (PFTC) was synthesized and used as a UF pretreatment agent in actual lake water treatment. The control mechanism of PFTC on membrane fouling was investigated from the perspective of organic removal efficiency and in-situ membrane surface regulation. PFTC demonstrated a remarkable affinity for soluble metabolic intermediates and hydrophilic proteins through complexation and hydrogen bonding force, achieving removal efficiencies of 66.4 % for UV254 and 81.3 % for DOC, respectively. The hydrophilic pollutants with high molecular weight and non-saturated structure could be preferentially removed by PFTC due to its diverse hydrolysates including positively charged Fe-based hydrolysates, amorphous Ti-based hydrolysates, and highly polymerized Fe-Ti copolymers. The flocs generated by PFTC exhibited strong hydrophilicity, allowing for the formation of a loose porous cake layer on the ultrafiltration membrane, which acted as a hydrophilic layer to enhance the anti-fouling performance of ultrafiltration membrane. With its dual function of contaminant removal and in-situ membrane surface regulation, PFTC alleviated 98.9 % of membrane fouling. This study provides new insights into membrane fouling control by coagulation pretreatment and efficient treatment of surface water.

Determination of aconitum alkaloids in acute poisoning case by electromembrane extraction

In this work, electromembrane extraction (EME) was used for the first time to separate aconitine (AC), mesaconitine (Mes-AC) and hypaconitine (Hyp-AC) from biological samples and Chinese herbal medicines. Efficient EME of polar and high molecular weight aconitine alkaloids from different sample matrices was achieved with the solvent of 1-ethyl-2-nitrobenzene (ENB). Under the optimal EME conditions, EME provided recoveries for all targets in the range of 72%–74 %, 85%–103 % and 92%–94 % for whole blood, urine and aqueous samples. The proposed EME systems combined with LC-MS/MS and HPLC-UV were evaluated using different sample matrices, and the methods displayed satisfactory analytical characteristic including negligible matrix effect. The LOD and LOQ of AC, Mes-AC, and Hyp-AC by EME-LC-MS/MS were in the range of 0.002–0.068 ng/mL and 0.005–0.228 ng/mL respectively. The LOD and LOQ of AC, Mes-AC, and Hyp-AC by EME-HPLC-UV were in the range of 0.06–0.26 μg/mL and 0.20–0.86 μg/mL, respectively. The coefficient of determination, R2-value was ≥0.9926 for all cases, and the accuracy in the linear ranges was in the range of 91%–111 %. Finally, the method was successfully applied for the qualitative and quantitative analysis of AC and Mes-AC in the whole blood and herbal medicine dreg samples from an actual forensic case, and poisoning by aconitum alkaloids was identified as the cause of death. Therefore, we believe that EME could be a powerful tool to identify poisoning, and EME has great potential for efficient separation of polar and high molecular weight substances. These are of great importance in the fields of but not limited to forensic science, Traditional Chinese Medicine and clinics.

Dissolution of denim waste in N-methyl morpholine-N-oxide monohydrate for fabrication of regenerated cellulosic film: Experimental and simulation study

Despite the significant amount of denim waste and its potential as a cellulose source, its use has been neglected. This study uses N-methyl morpholine-N-oxide, an eco-friendly solvent, to dissolve denim (including 100 % cotton) and create a denim film. Achieving a 10 % denim record solubility, a cellulosic film was also fabricated for comparison. Characterisation techniques were applied, and molecular dynamics simulations explored intramolecular interactions and the influence of indigo dye on dissolution process. FTIR spectra indicated no chemical reactions during dissolution and regeneration, though a shift in OH stretching suggested a change in crystallinity, confirmed by XRD results showing decreased crystallinity and a structural shift from cellulose I to cellulose II. 13C NMR analysis revealed disruptions in interchain hydrogen bonds after regeneration. TGA results showed lower decomposition temperatures for both films compared to the powders. Testing mechanical properties showed the denim film had higher elongation at break but lower tensile strength than the cellulose film. MD simulations indicated indigo dye did not significantly affect fundamental interactions but decreased denim solubility by reducing the diffusion coefficient. Rheological tests supported the simulation results, showing higher viscosity and molecular weight for the denim solution compared to cellulose.

Enhanced human activities since 20th century in pearl river delta, southern China: Evidence from high-resolution sedimentary records of polycyclic aromatic hydrocarbons and synthetic musks

To understand the environmental impact of anthropogenic activities, the high-resolution temporal and compositional variations of polycyclic aromatic hydrocarbons (PAHs), oxygenated PAHs, and synthetic musks, related to human activities were investigated in a sediment core taken from the Pearl River Estuary, southern China. The temporal trend of the target compounds was evidence of the considerable impact of anthropogenic activities in the Pearl River Delta. Two significant increases of the target compounds levels in the sediment core were aligned with two nodes of key periods of economic development in China, namely, the foundation of People's Republic of China (1950s) and China's accession to the World Trade Organization (2000s). Subsequently, the significant decline of the target compounds in sediments from the 2010s indicated the successful regulation of pollutant discharges and pollution control measures. The increase in the contribution of higher molecular weight PAHs suggested a potential transition from agricultural activities to industrial activities.

Review of Polycyclic Aromatic Hydrocarbons Pollution Characteristics and Carcinogenic Risk Assessment in Global Cooking Environments.

In recent years, research on air pollution in cooking environments has gained increasing attention, particularly studies related to polycyclic aromatic hydrocarbons (PAHs) pollution. Hence, it is crucial and urgent to conduct a comprehensive review of research findings and further evaluate their carcinogenic risks. This study adopts a comprehensive literature review approach, systematically integrating and deeply analyzing the conclusions and data from 62 selected relevant studies. It focuses on the impact of different factors on PAHs concentrations, considers the indoor-outdoor PAHs concentration ratio, and conducts carcinogenic risk assessments for PAHs. The results show that Africa has the highest average PAHs pollution concentration globally at 14.74μg/m³, exceeding that of other continents by 1.5 to 160.9 times. Among various influencing factors, fuel type has the most significant impact on PAHs concentrations. Existing research data indicate that cooking with charcoal as fuel produces the highest PAHs concentration at 223.52μg/m³, with high molecular weight PAHs accounting for 58.16%, significantly higher than when using clean energy. Furthermore, efficient ventilation systems have been proven to substantially reduce PAHs concentrations, with a reduction rate of up to 88.1%. However, cooking methods and food types also have a small but non-negligible impact on PAHs production. Using mild cooking methods such as steaming and selecting low-fat foods can also reduce PAHs to some extent. Additionally, through the analysis of the Indoor/Outdoor ratio, it was found that cooking is the primary source of indoor pollution, and the average concentration of PAHs in cooking environments in Asia and Africa is much higher than in Europe and America. The Total Incremental Lifetime Cancer Risk (TILCR) exceeds 10⁻⁴, indicating a high level of carcinogenic risk.

The dissolution of galactomannans in type II/III deep eutectic solvents: Effect of polysaccharide structure and interaction mechanism

Deep eutectic solvents (DESs) have garnered increasing attention as sustainable solvents for natural polysaccharides. Galactomannans (especially guar and locust bean gums) are abundant natural compounds used in food, medicine, agriculture and daily chemical products, whereas their high molecular weight and randomly distributed non-linear structures remain a huge challenge in solubilization and high value-added utilization. In this study, the dissolution of galactomannans in type II/III DESs was comprehensively investigated using density functional theory (DFT) calculation, experimental results, and molecular dynamics simulation (MD). The results indicated that immense anionic and neutral H-bonds supported by type II DESs (consisting of a quaternary ammonium salt and a metal chloride hydrate) could break and rebuild galactomannan H-bond networks, thereby exhibiting remarkable physical solubilization. A large number of active acid sites in type III DESs (consisting of a quaternary ammonium salt and a hydrogen bond donor) greatly improved solubility and cleaved the glycosidic bond, enabling the recovery of polysaccharides with a target molecular weight. Furthermore, significant correlations between solubility and the structure of galactomannans had been established, which meant that high molecular weight and rich galactose side-chains produced repulsive interactions with DESs, directly hindering dissolution. Overall, this work not only offered a framework for enhancing the dissolution of polysaccharides, but also proposed a promising strategy for development of task specific DESs promoting green chemistry and the use of sustainable bioresources.

Use of Renewable Alcohols in Autocatalytic Production of Aspen Organosolv Lignins.

This study aimed to investigate the intrinsic efficiency of renewable alcohols, applied under autocatalytic conditions, for removing lignin from aspen and hot-water-extracted aspen while substantially preserving the lignin structure so as to facilitate various valorization strategies. Ethylene glycol (EG), propylene glycol (PG), 1,4-butanediol (BDO), ethanol (EtOH), and tetrahydrofurfuryl alcohol (THFA) were evaluated based on their lignin solubilization ability, expressed as the relative energy difference (RED) following the principles of the Hansen solubility theory. The findings indicate that alcohols with a higher lignin solubilization potential lead to increased delignification, almost 90%, and produce a lignin with a higher content of β-O-4 bonds, up to 68% of those found in aspen milled wood lignin, thereby indicating their potential for valorization through depolymerization. However, these alcohols also produce lignin with a higher content of β-β and β-5 bonds, resulting in a higher molecular weight and polydispersity, due to readily occurring homolytic reactions. Hot-water extraction (HWE) conducted prior to alcohol treatment reduced the delignification efficiency and resulted in a lignin with a lower β-O-4 bond content. The lignins produced in these experiments exhibited a superior UV-A absorption capacity compared with synthetic benzophenone, as well as a greater radical quenching ability than synthetic butylated hydroxytoluene, indicating their potential for use in the protection of polymers against degradation.

Evaluation of morphology, physical and mechanical properties of hyaluronic acid matrices of various molecular weights by atomic force microscopy

Using atomic force microscopy the morphology of 1 and 2 % sodium hyaluronate solutions matrix with low molecular weight (LM) and high molecular weight (HM) hyaluronic acid (HA) fabricated by bioenzymatic synthesis was evaluated. The presence of a proteoglycan aggregate with processes of the core protein in the absence of sulfated glycosaminoglycans was established. The effect of irradiation with a light flux on the ordering of the HA matrix was observed. Intermolecular consolidation of high molecular HA was established. The elastic modulus of the matrix with LM and HM HA has also been determined.

Effect of branch length of cluster dextrin on the textural and rheological properties of κ-carrageenan emulsion gels

In this paper, a range of novel cluster dextrins (CDs) with high molecular weight (∼105 g/mol) and narrow molecular weight distribution were fabricated by α-amylase and branching enzyme (BE, EC 2.4.1.18). The influence of CDs on the physicochemical properties of κ-carrageenan (KC) emulsion gels was investigated. The average particle size of the composite emulsion gels containing CD was decreased by 7.85–12.66 μm, and the gel network was more uniform and denser, owing to stronger non-covalent interactions in the composite sample system. Textural results demonstrated that the composite emulsion gels exhibited higher hardness and springiness, but lower cohesiveness. CDs hindered the formation and aggregation of KC double helices, as evidenced by reducing the intensity of the sulfate group peak at 1223 cm−1. Furthermore, CDs increased the apparent viscosity, storage modulus (G'), and melting temperature (Tm) of emulsion gels, based on rheological results. CDs with longer branch lengths were more prone to entangle with KC chains to optimize the gel structure, exhibiting a more significant effect on the physicochemical properties of emulsion gels. The present study provided a new insight for constructing a new energy delivery system.

Valorization of lignin-rich solid residues from different eucalyptus wood conversion processes as oil structurants via electrospinning

The growing demand for sustainable materials has been driving research towards the use of biopolymers from natural resources. This study explores the valorization of lignin-rich solid residues derived from different eucalyptus wood conversion processes, specifically autohydrolysis (AHL), steam-explosion (SEL), and kraft pulping (EKL), via electrospinning. The potential of these electrospun nanostructures as eco-friendly oil structurant is investigated for lubricant applications. Solutions of AHL, SEL, and EKL fractions in a 3:1 v/v trifluoroacetic acid (TFA)/N,N-dimethylformamide (DMF) binary solvent were prepared at concentrations of 0.015, 0.03, and 0.05 g/mL. AHL and SEL samples exhibited superior spinnability due to higher carbohydrate content and molecular weight and lower ash content. Increasing the solution concentration to 0.05 g/mL resulted in the consecution of larger average fiber diameters (up to 0.44 and 0.39 μm, for AHL and SEL, respectively) and reduced bead formation. Stable oleo-dispersions were achieved solely with electrospun homogeneous nanofiber mats, while nanostructures predominantly composed of electrosprayed particles, like those obtained with EKL produced physically unstable dispersions from which the oil readily separates. The rheological response and microstructure of oleo-dispersions were significantly affected by both the conversion process of eucalyptus wood and the spinning solution concentration. The rheological properties of the oleo-dispersions can be tailored by modifying the spinning solution concentration, with G′ values ranging from 5·102 to 5·104 Pa and consistency and flow indices roughly ranging from 90 to 990 Pa sn and from 0.06 to 0.19, respectively, depending on the nature of the lignin-rich fraction and the type of electrospun nanostructure employed. These results highlight the potential of electrospun nanostructures obtained from lignin-rich solid residues in advanced materials applications, promoting the valorization of waste streams derived from different biorefinery processes, as well as the development of novel environmentally friendly lubricants.

Retrospective controlled study of the efficacy of very high molecular weight hyaluronic acid (VHMWHA) noncross-linked as a dermabooster for the improvement of elasticity in the skin.

Hyaluronic acid HA, regardless of its molecular weight, presentation and route of administration, is currently among the products most in-demand by our clients for the prevention and treatment of skin ageing in aesthetic medicine clinics.

Biodegradable thermoplastic elastomers synthesized from C7–C10 aliphatic dicarboxylic acids, 2-methyl-1,3-propanediol, and L-lactide

Elastic materials with high biodegradability should replace those with low biodegradability in some applications. We previously reported biodegradable thermoplastic elastomers (TPEs) composed of poly(l-lactide) (PLLA) as a hard segment and aliphatic polyesters from 2-methyl-1,3-propanediol (MP) and short aliphatic dicarboxylic acids as soft segments. In this study, we synthesized the biodegradable thermoplastic elastomers using longer aliphatic dicarboxylic acids to develop the TPEs with lower glass-transition temperature (Tg) and high biodegradability. A series of aliphatic polyesters were prepared by polycondensation of MP and aliphatic dicarboxylic acids bearing 7–10 carbons. Among them, poly(2-methyl-1,3-propylene azelate) (PMP9) was found to have lower Tg, amorphous nature, and high biodegradability in seawater. The ring-opening polymerization of l-lactide (LLA) using PMP9 as a macroinitiator afforded triblock copolymers, PLLA-b-PMP9-b-PLLA (TPE9). The successive addition of LLA to in-situ generated PMP9 resulted in the successful one-pot synthesis of high molecular weight TPE9. The TPE9s showed both low Tg of the PMP9 segment and high melting temperature of the PLLA segment. The TPE9s exhibited elastic behavior showing elongation at break of up to 2500 % in tensile tests and also high biodegradability in seawater. Thus, we developed potentially practical TPE with tunable physical properties and high biodegradability obtainable from easily available and renewable starting materials.

Abatement of algal extracellular organic matter by vacuum ultraviolet: Effect of dissolved oxygen and role of in-situ formed reactive oxygen species

Algal extracellular organic matter (EOM) in water produced during the outbreak of algal blooms is difficult to be effectively removed by conventional water treatment processes. Compared with ultraviolet (UV), vacuum ultraviolet (VUV) can additionally radiate 185 nm photons, and VUV can split water to produce reactive oxygen species (ROS) in-situ. Herein, abatement and characteristic variation of EOM under VUV irradiation and the mechanism were investigated. Results indicated that EOM abatement by VUV irradiation were significantly higher than that by UV irradiation. The mineralization rate constant of EOM under VUV was 2.25 times of that under UV. Besides, under VUV irradiation, the abatement efficiency of EOM was promoted with the increased dissolved oxygen (DO), and EOM with a lower initial concentration had a higher abatement efficiency. Intensities of characteristic fluorescence peaks of EOM decreased obviously after VUV irradiation, and removal rates of specific fluorescent organic components were ≥ 74.4%. Under VUV irradiation, organic matter in EOM with higher molecular weight was transformed into that with lower molecular weight. Moreover, hydroxyl radical (•OH) generated in-situ by VUV dissociating water with different DO was directly identified by fluorescence molecular probe technology, and the higher DO caused the higher production of •OH. Furthermore, the mechanism of EOM abatement by VUV was proposed. DO and the produced ROS enhanced the abatement efficiency of EOM, and they played important roles in EOM abatement. This study disclosed abatement characteristics of EOM under VUV irradiation and provided great value for expanding the utilization of VUV in water treatment.

Synthesis of High-Molecular-Weight Polypropylene Elastomer by Propylene Polymerization Using α-Diimine Nickel Catalysts.

The α-diimine late transition metal catalyst represents a new strategy for the synthesis of atactic polypropylene elastomer. Taking into account the properties of the material, enhancing the molecular weight of polypropylene at an elevated temperature through modifying the catalyst structure, and further increasing the activity of α-diimine catalyst for propylene polymerization, are urgent problems to be solved. In this work, two α-diimine nickel(II) catalysts with multiple hydroxymethyl phenyl substituents were synthesized and used for propylene homopolymerization. The maximum catalytic activity was 5.40 × 105 gPP/molNi·h, and the activity was still maintained above 105 gPP/molNi·h at 50 °C. The large steric hindrance of catalysts inhibited the chain-walking and chain-transfer reactions, resulting in polypropylene with high molecular weights (407~1101 kg/mol) and low 1,3-enchainment content (3.57~16.96%) in toluene. The low tensile strength (0.3~1.0 MPa), high elongation at break (218~403%) and strain recovery properties (S.R. ~50%, 10 tension cycles) of the resulting polypropylenes, as well as the visible light transmittance of approximately 90%, indicate the characteristics of the transparent elastomer.

Full Face Tailored Treatments Using Hyaluronan Dermal Fillers: Biophysical Characterization for Safe and Effective Approaches

Hyaluronic acid (HA)-based dermal fillers are among the most popular non-invasive facial aesthetic treatments. To ensure an effective and safe treatment experience, knowledge of their biophysical and rheological characteristics, such as: HA concentration, molecular weight (MW), G′, and the degree of cross-linking is essential. Products with a higher MW, G′, and degree of cross-linking are more suitable for promoting volume and lift. Dermal fillers with a lower MW, G′, and degree of cross-linking can produce a soft filling effect that regulates hydration and elasticity. This review discusses how these rheological characteristics can inform treatment choice and their effects on clinical outcomes. The Aliaxin® line of HA dermal fillers, which are tailored to different clinical applications due to their rheological characteristics, highlights that extensive knowledge of the product can provide very safe and effective procedures for patients, whilst respecting their natural facial aesthetics. This review discusses studies using Aliaxin® dermal fillers for volumizing and hydrating treatments and fillers that can be used for lip augmentation. Treatment with Aliaxin® was overall very effective, with no reported adverse events. A full facial treatment using tailored dermal fillers may be a future approach to achieve an effective and safe harmonized and natural aesthetic.