Polymeric materials were evaluated with regard to their spinnability and respective fibre diameters. A modified single fibre spinning device was firstly used to derive a novel generalised model, utilising process parameters (die diameter, throughput, and stretching relevant take-up pressures) and material properties (zero shear viscosity) to predict the diameter of polymeric fibres on the basis of four different polymers. Further evaluation of the resulting power law dependence was conducted on filaments produced via conventional melt spinning and meltblown processes. Fibres produced on the pilot machines showed close agreement with the model equation with only the need to adjust an easily calculable device dependent factor. The outcome of the presented work is a user-friendly model of high practical relevance, which can be used to predict the diameter of amorphous and semicrystalline polymeric fibres, independent of material and machine used with sufficient accuracy for fast estimations.

Vinyl acetate (VAc) was polymerized to about 90% conversion in 9 h at 40°C from the colloidal microstructure of the VAc/fumed silica/cetyltrimethylammonium bromide (CTAB) system. The glass transition () of poly(vinyl acetate) (PVAc) polymerized in these emulsion gels with silica was higher () than those of PVAc made from bulk polymerization at 60°C () and the weight average molar mass () was also larger ( about 300 kg/mol) than those from bulk polymerization (). Increased , , and lowered processing temperature for these composites could facilitate new applications for PVAc.

Salt water exposure conditions relevant to carbon-fibre-reinforced polymer (CFRP) prestressed concrete structures in marine environments are investigated. The diffusion into relatively small diameter CFRP tendons can be a lengthy process so the prediction of the long-term moisture uptake using short-term experiments on thin films of epoxy would be advantageous. However, the fibre inclusions within a composite introduce complexities, and factors are typically required for correlation with pure epoxy specimens. Diffusion parameters based on moisture uptake result from CFRP tendons exposed to salt water solution at 20°C and 60°C are compared with those obtained using equivalent thin film specimens. The higher temperature is selected to accelerate the moisture uptake. It is found that the measured ratios of tendon and epoxy diffusivity were temperature dependent, and the combination of the higher temperature and salt solution leads to an increased propensity for moisture uptake in the tendon. Existing analytical models to predict the CFRP tendon diffusivity from that of a thin film of epoxy did not appear to capture the observed trends. However, predictions using a unit cell with a fibre interface zone suggest that this may be due to an increased diffusivity in the interphase region.

In this study, both polyvinyl chloride (PVC) and polyacrylonitrile (PAN) were dissolved in dimethyl formaldehyde (DMF) with 8 wt. % concentrations at 25 : 75, 50 : 50, and 75 : 25 of PVC: PAN blending. For the investigation of the homogeneity and compatibility of mixture polymer solutions, it is examined by rheological properties such as viscosity, shear stress, shear rate, and calculation of the flow behavior index, while the investigation of the stability and high density of nanofibers without beads used field-emission scanning electron microscopy (FE-SEM), Fourier transform near-infrared spectroscopy (FT-NIR), X-ray diffraction (XRD), and differential scanning calorimetry-thermogravimetric analysis (DSC-TGA). The results show that blending of PAN with PVC leads to improving of the electro spun ability of PVC with more stability, and the mean nanofiber diameter was at 25 : 75 PVC: PAN. Moreover, mechanical properties are ultimate tensile strength and modulus of elasticity decreasing with decreasing the blending ration from pure PVC to 75 : 25 PVC: PAN nanofibers by 71% and 83%, respectively, while the elongation at break increases by 79%, and decomposition temperatures decreased from 451.96 to 345.38°C when changing the PVC content from pure PVC to 25 : 75 PVC: PAN. On the other hand, changing of the nanofiber behavior from hydrophobicity to hydrophilic increased the PAN content in PVC: PAN blends. Furthermore, the low interaction between the chains of polymers and the crystallinity (%) and crystalline size (nm) of blend nanofibers slightly decreased compared to the pure polymers. According to all tests, the 25: 75 PVC: PAN was the best blending ratio, which gave a more stable nanofiber produced at low concentrations and more compatible between the PVC and PAN.

Composites that were made stronger with jute fiber and glass fiber were used to test the performance of filament wound abaca fiber composites. Tensile, bending, and dynamic mechanical analyses were used to figure out the mechanical properties of the composites. Fiber composites and glass-fiber composites were found to have higher density and mechanical properties than abaca fiber-based composites. This is because resin did not get into the cell cavity of the fiber’s inner tissue structure. The abaca fiber composites that worked the worst were those in which the fibers were pulled out while the fibers on the surface were torn. The fiber-reinforced epoxy circumferential composite interface junction in the twisting abaca fiber circumferential composite was found to be more flexible and have a higher glass transition temperature than any of the other composites (6000 MPa). We found that twisting abaca fiber-naval ordnance laboratory and twisting abaca fiber-prepared circumferential composite had the lowest frequency dependence and performance variability. To improve composite properties, both the outside and inside structures of twisting abaca fiber need to be fixed. There is also a rise in fiber-to-resin contact and a rise in fiber surface area. The diameter of the fibers also gets smaller.

A unique orthogonal crosslinker-induced hydrogel, whose mechanical strength can be tunable by the crosslinker topology upon thermal treatment, is described herein. The crosslinker containing cationic moieties and crosslinkable styrenyl groups was employed for the preparation of orthogonally crosslinked hydrogels having ionic and covalent characteristics. The manipulation of the orthogonal crosslinkers topology and the ionic bond strength between cationic and anionic moieties facilitated the control of the mechanical properties. Short-term temporal modulation of hydrogel moduli, a key factor of the substrates for cell development, was demonstrated and could provide dynamic microenvironment for biological process. In addition, on-demand control of the elastic properties of the hydrogels by application of a thermal stimulus provides new avenues to regulate cell growth. Furthermore, the orthogonality of the crosslinkers allowed molecular functionalization of a wide range of molecules of interest to the hydrogels by thiol-ene Michael addition (nucleophilic addition of sulfhydryl and carbon-carbon double bonds) in a friendly manner as demonstrated in our work.

This study investigates the mechanical and thermal properties of biocomposite in relation to their hybridization. Compression moulding was utilised to produce hybrid biocomposites composed of polyester resin reinforced with kenaf, jute, and three distinct combinations of kenaf/jute fibers. To increase the bonding of kenaf and jute fibers with polyester resin, a 5 percent NaOH solution was administered to them. The following stacking sequences were used to manufacture a total of five different types of laminates: polyester resin 80 wt%/kenaf fiber 20 wt%, polyester resin 80 wt%/jute fiber 20 wt%), polyester resin 80 wt%/kenaf fiber 5 wt%/jute fiber 15 wt%, polyester resin 80 wt%/kenaf fiber 10 wt%/jute fiber 10 wt%, and polyester resin 80 wt%/kenaf fiber 15 wt%/jute fiber 5 wt%. In the mechanical and thermal tests, it was discovered that the polyester resin 80 wt%/jute fiber 20 wt% biocomposites had increased strength compared to the other hybrid biocomposites investigated.

Biodegradable and eco-friendly composite adsorbent was synthesized from modified jute fiber and gelatin and evaluated its efficacy in removing cadmium (Cd2+), lead (Pb2+), and chromium (Cr3+) ions from an aqueous solution. The prepared sample was characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, and energy dispersive X-ray analyses, which revealed that gelatin successfully intercalated into the microcrystalline cellulose matrix. In batch adsorption studies, the effects of pH, adsorbent dosage, initial metal ions concentration, and temperature on the removal of heavy metal ions were investigated. The adsorption capacity of the composite varied with changing parameters, and the maximum removal efficiency obtained for Cd2+, Pb2+, and Cr3+ was 95%, 88%, and 70%, respectively, at pH 6 with 60 ppm of each metal ions concentration and an adsorbent dosage of 1.0 g L−1. Different functional groups in composite adsorbent facilitated heavy metal ions adsorption. Five error analysis methods were used to evaluate the fit the goodness of the data. The equilibrium adsorption and kinetic data were well-fitted with the Langmuir isotherm model and pseudo-second-order, respectively. Moreover, the thermodynamic study showed that the adsorption was spontaneous, chemisorption, and endothermic. Our work offers a sustainable and biodegradable composite synthesized from modified jute fiber and gelatin for multimetal ions removal from an aqueous, which is an eco-friendly alternative to conventional nonbiodegradable adsorbents with potential environmental risks.

Drilling in synthetic fiber-reinforced polymer composites is facing challenges due to their anisotropic, inhomogeneity, and abrasive machining behavior. The joining of composite parts using fasteners is commonly done by the drilling, and the generated heat is one of the main causes to damage the drilled hole in the composite. Moreover, the quality of drilled hole is crucial for joining parts effectively. The paper presents the design, fabrication, and drilling of a hybrid fiber-reinforced polymer (HFRP) based on insulative coating. These composites were fabricated using vacuum infusion molding (VIM) and coated with different thicknesses to investigate the influence of drilling parameters and associated damages. Cutting speed, feed rate, and coating thicknesses were varied, and a full factorial design of the experiment was formulated. High-speed steel (HSS) twist drill bit was used to drill the coated composite and test samples, and delamination factor and surface roughness were measured. ANOVA and full factorial response optimizer were used to evaluate the influence and optimum drilling parameters. The delamination factor (DF) at the entry and surface roughness were found to decrease with the increasing cutting speed. However, the DF at the exit showed the opposite. Coating thickness influenced the delamination at the entry whereas delamination at the exit has been found insignificant. For drilling HFRP composite with 1 mm coating thickness, 3000 RPM spindle speed and 0.08 mm/rev feed rate were found optimum parameters in minimizing surface roughness and delamination damage. However, 6000 RPM and 0.02 mm/rev were found optimum parameters for drilling HFRP composite with 1.5 mm coating thickness.

Graft modifications of PVDF fluoropolymers have been identified as the efficient route to improve the properties and expand the applications. Taking advantage of C-F and C-Cl bonds in the repeat units, atom transfer radical polymerizations (ATRP) were widely used for graft modification. Recently, photoinduced ATRP has shown good spatial and temporal control over the polymerization process in contrast to thermal activation mode. This minireview highlights the progress in PVDF-based fluoropolymer modifications by using photoinduced Cu(II)-mediated ATRP and organocatalyzed ATRP. The challenges and opportunities are proposed with the aim at advancing the development of synthesis and applications of fluoropolymer.

Mine tires are an essential and expensive component of heavy mining machinery. This study explored the grounding characteristics and temperature field distribution of mining tires during driving as well as the relationships between the maximum temperature and tire inflation pressure, load, and speed. Two-dimensional and three-dimensional finite element models of mine tires were established. Steady-state rolling simulation analysis was conducted based on inflation and static load simulations. Temperature field simulation analysis was conducted with the tire section as a research object. The accuracy of the finite element model was verified. Analysis results demonstrated that the grounding contact area decreased with an increase in charging pressure and increased with an increase in load. With an increase in inflation pressure, the maximum normal grounding stress increased in the middle part of the tread and decreased near the shoulder. The maximum normal grounding stress continuously deviated in the shoulder direction with an increase in load. Temperature field analysis indicated that the tire had the maximum temperature at the binder position, where the first belt layer was connected to the second belt layer, which corresponds to the maximum stress position in the steady-state rolling simulations. Tire temperature increased with driving speed. The maximum temperature increased with an increase in tire deflection, whereas the deflection decreased with an increase in inflation pressure and increased with an increase in load. Speed had the greatest influence on the maximum temperature, followed by load, with inflation pressure having the smallest influence. The results of this research can be used to improve the service life of mine tires to improve productivity and reduce costs.

To manage the polycotton textile-waste fabric (PCWF), a modified alkaline hydrolysis method is used for decolorization and separation of polyester as terephthalic acid (TPA). The effects of optimum conditions on TPA yield (%) have been determined to be . Dye degradations and K/S values are measured by UV-visible spectrophotometer. K/S value of PCWF is 37.06 and separated cotton fabric (SCF) is 0.035, respectively. The chemical functionalities and crystallinity of PCWF, SCF, and TPA are determined by using FTIR and XRD. FTIR peak values are 1684 cm-1, 1574 cm-1, 1512 cm-1, 1280 cm-1, and 1425 cm-1 that prove transformation of polyester to TPA. XRD peaks confirm polyester conversion to TPA, and the values are 17.4, 25.13, 28.12, 29.09, and 38.7. TGA, SEM, and EDX data showed the thermal stability, morphology, and elemental composition of TPA.

The catalyst synthesis of salicylaldimine Ni(II) complexes with bulky imide moieties, ethylene polymerization, and characterization of synthesized polyethylenes are described in this paper. These Ni(II) complexes are designed to bear 2-aminobiphenyl and 4-tritylaniline. Results confirmed relatively high activity (up to g PE mol Ni-1 h-1) of these catalysts in ethylene polymerization. Moreover, Ni(II) complexes demonstrated enhanced thermal stability, maintaining activity level up to 80°C. The generated polyethylenes possess moderate branching density and high melting temperatures. Less bulky 2-aminobiphenyl group resulted in higher branch content, while in Ni(II) complexes bearing 4-tritylaniline, more linear structure was observed. These semicrystalline polyethylenes showed mechanical properties similar to thermoplastics.

Superabsorbent polymer (SAP) is a new water-retaining and nutrient-holding material with the potential to improve soil properties and promote crop growth in arid and semiarid areas. This study investigated the effects of multifunctional SAP on the sandy soil properties and maize productivity in Yanghuang irrigated area of Ningxia where residue incorporation was a common agricultural practice, we tested multifunctional SAP at different doses of 0, 30, 60, 90, and 120 kg ha–1 under the residue incorporation to the field. The soil bulk density in the 0–0.40 m layer was significantly lower by 6.2–8.2% under SAP at 60–120 kg ha–1 compared with no SAP, but the total soil porosity was improved significantly by 8.5–11.2%, where the SAP at 90 and 120 kg ha–1 had the greatest effects. The applications of SAP at 60 and 90 kg ha–1 significantly improved soil organic matter, and available and contents in the 0–0.40 m soil layer. The soil water storage (0–1.0 m) under SAP at 60–120 kg ha–1 was significantly increased by 17.1–18.7% compared with no SAP throughout the whole maize growing season. The SAP at 60–90 kg ha–1 significantly promoted crop growth and maize yield formation, and increased grain yield, whereas the net income were the highest with applying SAP at 30–60 kg ha–1. In combination with the soil physicochemical property, crop productivity and economic benefit comprehensive analysis of this two-year study, we recommended that the application of multifunctional SAP at 30–60 kg ha–1 under residue incorporation significantly improved the sandy soil properties, as well as increasing maize growth, crop productivity, and obtain the higher net income for farmers in Yanghuang irrigation area of Ningxia, China.

This work shows the possibility to employ sulfonated tetrafluoroethylene-based fluoropolymer-copolymer, commercially known as Nafion, as a sensible layer on sensors to detect organic solvents such as ketones. The detection and evaluation of ketone corpuses is very important for multiple applications on medicine, specially to detect and evaluate diabetes mellitus from the breath of patients. Nafion is a very stable copolymer, easily available and relatively inexpensive. This allows us to envision the possibility of having cheap and reliable sensors to detect vapors of these substances based on this copolymer. The main result of the present work is that Nafion can protonate gaseous ions from organic solvents, such as acetone and similar substances, which modify its electrical properties, presenting a differentiated behavior according to the chemical nature of these substances, which could lead to their identification, designing an electrical nose, because each behavior is a fingerprint of the substance to detect. Then, this material can be used in the design of electrical sensors, which can be inexpensive, reliable, and chemically stable, representing an excellent alternative to ceramic sensors.

Wet blue leather is a waste produced by the leather industry. It is a difficult waste product to dispose of, and if not disposed of properly, it will affect the environment and cause toxicity. Therefore, recycling was considered as an alternative to waste disposal. In this study, polymer composites were prepared from two types of polymers, poly(butylene adipate-co-terephthalate) (PBAT) and poly(butylene succinate) (PBS), and wet blue leather (WBL). A twin screw extruder and injection molding were used to prepare the composites. The effect of polymer type and WBL content (5, 10, and 15 wt%) on mechanical properties, thermal properties, flammability, MFI, water absorption, and morphology was investigated. All the polymer composites showed an increase in tensile and flexural strength, Young’s modulus, and water absorption but decreased in elongation at break, impact strength, and flammability compared to neat polymers.

In this study, a series of polyoxymethylene copolymers are synthesized by bulk cationic ring-opening polymerization by 1,3,5-trioxane (TOX) with 1,3-dioxolane (DOX), octamethylcyclotetrasiloxane (D4), and cyclohexane oxide (CHO) as the second monomer using phosphotungstic acid (PTA) as an initiator. The polymer products were characterized by hydrogen nuclear magnetic resonance (1H-NMR), infrared spectroscopy (IR), thermogravimetry (TG), and differential scanning calorimetry (DSC). And the copolymerization energy barrier was calculated at the b3lyp/6-31g(d) calculation level using density functional theory (DFT) to explore the copolymerization ability of the second monomer with 1,3,5-trioxane. The results showed that CHO as the second monomer more easily participated in the copolymerization reaction, and the copolymers showed better thermal stability.

Recovery of fat-and-oil production wastes will reduce the technogenic impact on the environment, as well as involve them in a new production cycle as a secondary material resource. As part of solving this problem, the possibilities of using fat-and-oil production wastes in the production of a tyre reclaim and a modified tyre reclaim are considered. In the course of the studies, the fat-and-oil industry wastes’ sorption characteristics are determined, and in relation to oils in static and dynamic conditions, the spent reagent reclamation ways are determined. The authors obtained a tyre reclaim and a modified tyre reclaim using the fat-and-oil industry wastes (soap stock, diatomite, bleaching clay, and fatty acids isolated from soap stock). In this work, the authors studied the possibility of using the fat-and-oil industry wastes in the formulations of a tyre reclaim and a modified tyre reclaim. Extended physical and mechanical tests of experimental rubbers led to the conclusion that it is most expedient to use the fat-and-oil industry wastes in the formulation of rubber compounds for production of sleeper pads for railroad tracks, since when using a tyre reclaim and a modified tyre reclaim, the indicators of rubber properties practically do not change and comply with control standards.

The effects of prepolymerization, temperature, and hydrogen concentration on propylene bulk polymerization with a commercial Ziegler-Natta catalyst were investigated, and the apparent polymerization rate constants were estimated by varying reaction temperatures, hydrogen partial pressures, and polymerization methods. It was shown that prepolymerization has different effects on the polymerization rate and isotacticity of the polymer; without prepolymerization, the polymerization rate and isotacticity reach their maximum at 70°C and 80°C, respectively, whereas the polymerization rate and isotacticity with prepolymerization increase with the polymerization temperature in the range of 50-80°C. Moderate prepolymerization time reduced the fine fraction while increasing polymerization rate and isotacticity. Appropriate prepolymerization technique can increase mass transfer performance and fragmentation, which is a promising way to improve polymerization rate, isotacticity index, and fine fraction. Otherwise, insufficient prepolymerization or excessive prepolymerization causes prepolymer particle fragmentation.

The unique attributes, biodegradability, biocompatibility, perfect accessibility, and low production costs led to the use of natural gums in a different section of our lives. Among them, we can mention gums obtained from microorganisms (xanthan gum and gellan gum), plant tissues (Arabic gum and gum tragacanth), seeds (konjac gum and guar gum), seaweeds (alginates, agar gum, and carrageenans). Gums have essential applications in the medical and pharmaceutical, food, biotechnology, and critical agricultural industries. Encapsulation is one of the new methods to increase the stability of bioactive compounds during processing and storage. Encapsulation technology using natural gums is a new way to improve the performance of microbial agents in various sciences, especially agriculture, which represents a bright future in this field.