Synthesis of Biobased Poly(butylene Furandicarboxylate) Containing Polysulfone with Excellent Thermal Resistance Properties.

A synthetic biopolymer derived from furandicarboxylic acid monomer and hydroxyethyl-terminated poly(ether sulfone) is presented. The synthesis involves 4,4'-dichlorodiphenyl sulfone and 4,4-dihydroxydiphenyl sulfone, resulting in poly(butylene furandicarboxylate)-poly(ether sulfone) copolyesters (PBFES) through melt polycondensation with titanium-catalyzed polymerization. This facile method yields segmented polyesters incorporating polysulfone, creating a versatile group of high-temperature thermoplastics with adjustable thermomechanical properties. The PBFES copolyesters demonstrate an impressive tensile modulus of 2830 MPa and a tensile strength of 84 MPa for PBFES55. Additionally, the poly(ether sulfone) unit imparts a relatively high glass transition temperature (Tg), ranging from 36.6 °C for poly(butylene 2,5-furandicarboxylate) to 112.3 °C for PBFES62. Moreover, the complete amorphous film of PBFES exhibits excellent transparency and solvent resistance, making it suitable for applications, such as food packaging materials.

Identification and characterization of GLYCEROLIPASE A1 for wound-triggered JA biosynthesis in Nicotiana benthamiana leaves.

Although many important discoveries have been made regarding the jasmonate signaling pathway, how jasmonate biosynthesis is initiated is still a major unanswered question in the field. Previous evidences suggest that jasmonate biosynthesis is limited by the availability of fatty acid precursor, such as ⍺-linolenic acid (⍺-LA). This indicates that the lipase responsible for releasing α-LA in the chloroplast, where early steps of jasmonate biosynthesis take place, is the key initial step in the jasmonate biosynthetic pathway. Nicotiana benthamiana glycerol lipase A1 (NbGLA1) is homologous to N. attenuata GLA1 (NaGLA1) which has been reported to be a major lipase in leaves for jasmonate biosynthesis. NbGLA1 was studied for its potential usefulness in a species that is more common in laboratories. Virus-induced gene silencing of both NbGLA1 and NbGLA2, another homolog, resulted in more than 80% reduction in jasmonic acid (JA) biosynthesis in wounded leaves. Overexpression of NbGLA1 utilizing an inducible vector system failed to increase JA, indicating that transcriptional induction of NbGLA1 is insufficient to trigger JA biosynthesis. However, co-treatment with wounding in addition to NbGLA1 induction increased JA accumulation several fold higher than the gene expression or wounding alone, indicating an enhancement of the enzyme activity by wounding. Domain-deletion of a 126-bp C-terminal region hypothesized to have regulatory roles increased NbGLA1-induced JA level. Together, the data show NbGLA1 to be a major lipase for wound-induced JA biosynthesis in N. benthamiana leaves and demonstrate the use of inducible promoter-driven construct of NbGLA1 in conjunction with its transient expression in N. benthamiana as a useful system to study its protein function.

Electrocatalytic hydrogenation of indigo by NiMoS: energy saving and conversion improving.

An NiMo alloy bonded with sulfur (NiMoS) exhibits enhanced surface affinity toward water and organic molecules, thereby enhancing electrocatalytic hydrogenation (ECH) reactions through synergistic effects. In industrial processes, indigo, an ancient dye employed in the denim industry, is typically chemically reduced using sodium dithionite. However, this process generates an excess of toxic sulfide, which heavily contaminates the environment. ECH is a sustainable alternative for indigo reduction due to its reduced reliance on chemicals and energy consumption. In this study, carbon-felt (CF)-supported NiMoS was synthesized in a two-step process. First, the NiMo alloy was electrodeposited onto the CF surface, followed by sulfidation in an oven at 600 °C. NiMoS exhibits a larger electrochemically active surface area and a smaller charge transfer resistance compared to pure Ni and NiMo. Furthermore, NiMoS demonstrates excellent thermodynamic and kinetic properties for water splitting in strong alkaline solutions (1.0 M KOH). Additionally, optimal reaction conditions for the ECH of indigo were explored. Under the conditions of a 1.0 M KOH hydroxide medium with 10% methanol (v/v), an indigo concentration of 5 g L-1, a reaction temperature of 70 °C, and a current density of 10 mA cm-2, NiMoS/CF achieved remarkable improvements in both conversion (99.2%) and Faraday efficiency (38.1%). The results of this experimental work offer valuable insights into the design and application of novel catalytic materials for the ECH of vat dyes, opening up new possibilities for sustainable and environmentally friendly processes in the dye industry.

Hybrid hemp/glass fiber reinforced high-temperature shape memory photopolymer with mechanical and flame-retardant analysis.

Cultivated natural fibers have a huge possibility for green and sustainable reinforcement for polymers, but their limited load-bearing ability and flammability prevent them from wide applications in composites. According to the beam theory, normal stress is the maximum at the outermost layers but zero at the mid-plane under bending (with (non)linear strain distribution). Shear stress is the maximum at the mid-plane but manageable for most polymers. Accordingly, a laminated composite made of hybrid fiber-reinforced shape memory photopolymer was developed, incorporating strong synthetic glass fibers over a weak core of natural hemp fibers. Even with a significant proportion of natural hemp fibers, the mechanical properties of the hybrid composites were close to those reinforced solely with glass fibers. The composites exhibited good shape memory properties, with at least 52% shape fixity ratio and 71% shape recovery ratio, and 24 MPa recovery stress. After 40 s burning, a hybrid composite still maintained 83.53% of its load carrying capacity. Therefore, in addition to largely maintaining the load carrying capacity through the hybrid reinforcement design, the use of shape memory photopolymer endowed a couple of new functionalities to the composites: the plastically deformed laminated composite beam can largely return to its original shape due to the shape memory effect of the polymer matrix, and the flame retardancy of the polymer matrix makes the flammable hemp fiber survive the fire hazard. The findings of this study present exciting prospects for utilizing low-strength and flammable natural fibers in multifunctional load-bearing composites that possess both flame retardancy and shape memory properties.

Acetic acid positively modulates proline metabolism for mitigating PEG-mediated drought stress in Maize and Arabidopsis.

Introduction: Osmotic imbalance is one of the major consequences of drought stress, negatively affecting plant growth and productivity. Acetic acid has modulatory roles in osmotic balance in plants; however, the mechanistic insights into acetic acid-mediated osmotic adjustment under drought stress remains largely unknown. Methods: Here, we investigated how seed priming and seedling root treatment with acetic acid enabled maize plants overcoming polyethylene glycol (PEG)-induced drought effects. Results: Maize seeds primed with acetic acid showed better growth performance when compared with unprimed seeds under PEG application. This growth performance was mainly attributed to improved growth traits, such as fresh weight, dry weight, length of shoots and roots, and several leaf spectral indices, including normalized difference vegetation index (NDVI) and chlorophyll absorption in reflectance index (MCARI). The levels of oxidative stress indicators hydrogen peroxide (H2O2) and malondialdehyde (MDA) did not alter significantly among the treatments, but proline content as well as the expression of proline biosynthetic gene, Δ1-PYRROLINE-5-CARBOXYLATE SYNTHETASE 1 (P5CS1) was significantly elevated in plants receiving acetic acid under PEG-treatments. On the other hand, treating the seedlings root with acetic acid led to a significant recovery of maize plants from drought-induced wilting. Although growth traits remained unchanged among the treatments, the enhancement of leaf water content, photosynthetic rate, proline level, expression of P5CS1, and antioxidant enzyme activities along with reduced level of H2O2 and MDA in acetic acid-supplemented drought plants indicated a positive regulatory role of acetic acid in maize tolerance to drought. Moreover, the high expression of P5CS1 and the subsequent elevation of proline level upon acetic acid application were further validated using wild type and proline biosynthetic mutant p5cs1 of Arabidopsis. Results showed that acetic acid application enabled wild type plants to maintain better phenotypic appearance and recovery from drought stress than p5cs1 plants, suggesting a crosstalk between acetic acid and proline metabolism in plants under drought stress. Discussion: Our results highlight the molecular and intrinsic mechanisms of acetic acid conferring plant tolerance to drought stress.

Boron supply restores aluminum-blocked auxin transport by the modulation of PIN2 trafficking in the root apical transition zone.

The supply of boron (B) alleviates the toxic effects of aluminum (Al) on root growth; however, the mechanistic basis of this process remains elusive. This study filled this knowledge gap, demonstrating that boron modifies auxin distribution and transport in Al-exposed Arabidopsis roots. In B-deprived roots, treatment with Al induced an increase in auxin content in the root apical meristem zone (MZ) and transition zone (TZ), whereas in the elongation zone (EZ) the auxin content was decreased beyond the level required for adequate growth. These distribution patterns are explained by the fact that basipetal auxin transport from the TZ to the EZ was disrupted by Al-inhibited PIN-FORMED 2 (PIN2) endocytosis. Experiments involving the modulation of protein biosynthesis by cycloheximide (CHX) and transcriptional regulation by cordycepin (COR) demonstrated that the Al-induced increase of PIN2 membrane proteins was dependent upon the inhibition of PIN2 endocytosis, rather than on the transcriptional regulation of the PIN2 gene. Experiments reporting on the profiling of Al3+ and PIN2 proteins revealed that the inhibition of endocytosis of PIN2 proteins was the result of Al-induced limitation of the fluidity of the plasma membrane. The supply of B mediated the turnover of PIN2 endosomes conjugated with indole-3-acetic acid (IAA), and thus restored the Al-induced inhibition of IAA transport through the TZ to the EZ. Overall, the reported results demonstrate that boron supply mediates PIN2 endosome-based auxin transport to alleviate Al toxicity in plant roots.

Organelles and phytohormones: a network of interactions in plant stress responses.

Phytohormones are major signaling components that contribute to nearly all aspects of plant life. They constitute an interconnected communication network to fine-tune growth and development in response to the ever-changing environment. To this end, they have to coordinate with other signaling components, such as reactive oxygen species and calcium signals. On the one hand, the two endosymbiotic organelles, plastids and mitochondria, control various aspects of phytohormone signaling and harbor important steps of hormone precursor biosynthesis. On the other hand, phytohormones have feedback actions on organellar functions. In addition, organelles and phytohormones often act in parallel in a coordinated matter to regulate cellular functions. Therefore, linking organelle functions with increasing knowledge of phytohormone biosynthesis, perception, and signaling will reveal new aspects of plant stress tolerance. In this review, we highlight recent work on organelle-phytohormone interactions focusing on the major stress-related hormones abscisic acid, jasmonates, salicylic acid, and ethylene.

Constitutive expression of JASMONATE RESISTANT 1 induces molecular changes that prime the plants to better withstand drought.

In this study, we investigated Arabidopsis thaliana plants with altered levels of the enzyme JASMONATE RESISTANT 1 (JAR1), which converts jasmonic acid (JA) to jasmonoyl-l-isoleucine (JA-Ile). Analysis of a newly generated overexpression line (35S::JAR1) revealed that constitutively increased JA-Ile production in 35S::JAR1 alters plant development, resulting in stunted growth and delayed flowering. Under drought-stress conditions, 35S::JAR1 plants showed reduced wilting and recovered better from desiccation than the wild type. By contrast, jar1-11 plants with a strong reduction in JA-Ile content were hypersensitive to drought. RNA-sequencing analysis and hormonal profiling of plants under normal and drought conditions provided insights into the molecular reprogramming caused by the alteration in JA-Ile content. Especially 35S::JAR1 plants displayed changes in expression of developmental genes related to growth and flowering. Further transcriptional differences pertained to drought-related adaptive systems, including stomatal density and aperture, but also reactive oxygen species production and detoxification. Analysis of wild type and jar1-11 plants carrying the roGFP-Orp1 sensor support a role of JA-Ile in the alleviation of methyl viologen-induced H2 O2 production. Our data substantiate a role of JA-Ile in abiotic stress response and suggest that JAR1-mediated increase in JA-Ile content primes Arabidopsis towards improved drought stress tolerance.

Recent Developments of Tin (II) Sulfide/Carbon Composites for Achieving High-Performance Lithium Ion Batteries: A Critical Review.

The ever-increasing worldwide energy demand and the limited resources of fossil have forced the urgent adoption of renewable energy sources. Additionally, concerns over CO2 emissions and potential increases in fuel prices have boosted technical efforts to make hybrid and electric vehicles more accessible to the public. Rechargeable batteries are undoubtedly a key player in this regard, especially lithium ion batteries (LIBs), which have high power capacity, a fast charge/discharge rate, and good cycle stability, while their further energy density improvement has been severely limited, because of the relatively low theoretical capacity of the graphite anode material which is mostly used. Among various high-capacity anode candidates, tin (II) sulfide (SnS2) has been attracted remarkable attention for high-energy LIBs due to its enormous resource and simplicity of synthesis, in addition to its high theoretical capacity. However, SnS2 has poor intrinsic conductivity, a big volume transition, and a low initial Coulombic efficiency, resulting in a short lifespan. SnS2/carbon composites have been considered to be a most promising approach to addressing the abovementioned issues. Therefore, this review summarizes the current progress in the synthesis of SnS2/carbon anode materials and their Li-ion storage properties, with special attention to the developments in Li-based technology, attributed to its immense current importance and promising prospects. Finally, the existing challenges within this field are presented, and potential opportunities are discussed.

Bioreduction (AuIII to Au0) and stabilization of gold nanocatalyst using Kappa carrageenan for degradation of azo dyes.

Colloidal gold nanoparticles (AuNPs) have been used in high technology applications due to their optical and electronic properties. Unfortunately, these broader applications are severely hampered by their agglomeration tendency and instability. Therefore, in this study, highly stable and aggregation resistant AuNPs were synthesized using Kappa carrageenan (κ-car) media (as a reducing and stabilizing agent) by a green synthesis protocol. The effect of different factors of reaction such as the concentration of κ-car (Cκ-car %), reaction time (t), temperature (T), and solution pH (here after simply define to 'reaction parameters') was studied by one-variable-at-a-time technique to optimize the yield production of AuNPs. The characterization of AuNPs synthesized at optimum conditions revealed that the particles are spherical in shapes, smaller in size (13.5 ± 5.1 nm) with a narrow distribution, highly crystalline (d-spacing = 0.230 nm) in nature, well stabilized (zeta potential = -22.1 mV) by coating by a thin layer of κ-car carbohydrate. The synthesized AuNPs reveal excellent catalytic function in the degradation (up to 99%) of azo-dyes. The kinetics study in the degradation reaction revealed that the technique could be extended to real wastewater treatment applications.

Simple Amphoteric Charge Strategy to Reinforce Superhydrophilic Polyvinylidene Fluoride Membrane for Highly Efficient Separation of Various Surfactant-Stabilized Oil-in-Water Emulsions.

Long-term efficient separation of highly emulsified oily wastewater is challenging. Reported herein is the preparation of a reinforced superhydrophilic, underwater superoleophobic membrane with demulsification properties using active iron nanoparticles in situ generated on a polydopamine (PDA)/polyethylenimine (PEI)-modified polyvinylidene fluoride (PVDF) membrane surface. A stable zwitterionic structure is fabricated on the membrane surface and provides it with an excellent capability of binding a hydration layer, leading to enhanced superhydrophilic/underwater superoleophobic properties. The interaction between the membrane surface and water is quantified using the relaxation time of water. After iron nanoparticles in situ anchoring, the superhydrophilic, underwater superoleophobic PDA/PEI modified PVDF membrane shows more stable flux behaviors, higher oil separation efficiency, demulsification, and excellent antioil-fouling properties for various anionic, nonionic, and cationic surfactant-stabilized oil-in-water emulsions in a crossflow filtration system. The reinforced hydration layer and the amphoteric charged demusification properties of the membrane play important roles in enhancing the membrane separation performance. The reinforced membrane also exhibits excellent cleaning and reusability performance in long-term operations. The outstanding separation performance, as well as the simple and cost-effective fabrication process of the membrane with various favorable properties, highlight its promise in practical emulsified oily water applications.

Graphene oxide modified membrane for highly efficient wastewater treatment by dynamic combination of nanofiltration and catalysis.

Stacked graphene oxide (GO) nano-sheets with plentiful nanopores incorporated onto polymeric membrane are promising for water purification. However, maintaining high water permeability without sacrificing separation efficiency remains a challenge. Delamination of the GO layer from the membrane surface is another bottleneck affecting the efficiency of the material. To solve those problems, we immobilized a chemically crosslinked GO composite layer with enlarged interlayer space on the surface of a novel catalytic membrane, which served as the support. The modified GO nanosheets-coated catalytic membranes showed excellent separation robustness with withstanding strong lateral shear force during 6 h filtration in a crossflow model. The as-prepared membrane showed high removal efficiencies to Congo red and Basic blue (99 % and 96 %, respectively) due to the surface-coated GO composite layer. Furthermore, while launching the catalytic function of the membrane with a trace amount of reducing agent (NaBH4), the GO-coated composite membrane successfully purified 50 ppm Methyl orange, 50 ppm Methylene blue, 50 ppm Rhodamine B and 0.272 mmol/L 4-Nitrophenol to break through the membrane rejection limitation of 500 Mw. Combining nano-filtration and catalysis, the GO-coated composite membranes showed great potential for the continuous purification of chemically contaminated water.

Hierarchically Active Poly(vinylidene fluoride) Membrane Fabricated by In Situ Generated Zero-Valent Iron for Fouling Reduction.

Sodium hypochlorite (NaClO) solution is a typical cleaning agent for membrane fouling. However, it can damage membrane chemical structures and produce toxic disinfection byproducts, which in turn reduces the membrane performance. This study focuses on the fabrication of active membranes thereby overcoming the limitations of chemical cleaning. A hierarchical active poly(vinylidene fluoride) membrane with polydopamine/polyethyleneimine (PEI) co-supported iron nanoparticle (Fe NP) catalysts was successfully constructed and denoted as a Fe-HP-membrane. The Fe-HP-membrane exhibited excellent advanced oxidation activity with maximum flux recoveries (∼85% with bovine serum albumin [BSA] and ∼95% with humic acid [HA] solutions). After the static experiment of ∼30 days, the BSA proteins and HA successfully desorbed from the membrane surface. Especially, with a trace amount of hydrogen peroxide (H2O2) flowing over the surface of the Fe-HP-membrane, highly exposed active sites were observed. Membrane cleaning showed that the "outside-to-in" active surfaces generated considerable amounts of •OH radicals at the interface of BSA or HA and the fouled membrane. As a result, the unwanted foulants were successfully removed from the membrane interface, enabling multiple use of the Fe-HP-membrane. Therefore, backwashing with a small amount of H2O2 (0.33 wt %) covered ∼20% of the flux. In contrary, backwashing with NaClO (1 wt %) can only achieve a flux recovery of ∼10% after six consecutive BSA filtration cycles. The Fe-HP-membrane exhibited better HA foulant removal (a flux recovery of ∼51%) after backwashing with H2O2 than using NaClO (a flux recovery of ∼43%). Our findings demonstrate a new platform for water treatment and regeneration of fouled membranes.

A Novel Coloration of Polyester Fabric through Green Silver Nanoparticles (G-AgNPs@PET).

This paper reports a novel route for the coloration of polyester fabric with green synthesized silver nanoparticles (G-AgNPs@PET) using chitosan as a natural eco-friendly reductant. The formation of AgNPs was confirmed by UV-visible spectroscopy. The morphologies and average particles size of G-AgNPs was investigated by transmission electron microscope (TEM) analysis. The uniform deposition of G-AgNPs on the PET fabric surface was confirmed with scanning electron microscopy (SEM) and Fourier transform infrared (FT-IR) spectroscopy. The thermal properties were investigated using a thermogravimetric analyzer (TGA). The coloration and fastness properties of fabric were found to be significantly improved, a result related to the surface plasmon resonance of G-AgNPs. The antibacterial properties of fabric were also found to be excellent as more than 80% bacterial reduction was noticed even after 10 washing cycles. Overall, the proposed coating process using green nanoparticles can contribute to low-cost production of sustainable textiles.