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The purpose of this paper is to prepare amphiphilic block copolymers polyethylene adipate-block-polyethylene glycol (PEA-b-PEG)s and study their performance as plasticizers in rotogravure ink formulations.

Series of amphiphilic block copolymers (PEA-b-PEG1), (PEA-b-PEG2), (PEA-b-PEG3), (PEA-b-PEG4) and (PEA-b-PEG5) were prepared by the reaction of adipic acid, ethylene glycol and polyethylene glycol of different molecular weights (300, 1,000, 2,000, 10,000 and 20,000 g/mol), respectively. Full characterization of the prepared copolymers was achieved using Fourier Transfer Infrared Spectroscopy (FTIR), 1H NMR, thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC). The performance of the prepared copolymers as plasticizers for neat nitrocellulose resin were studied in different formulations, namely, R1, R2, R3, R4 and R5 containing copolymers (PEA-b-PEG1), (PEA-b-PEG2), (PEA-b-PEG3), (PEA-b-PEG4) and (PEA-b-PEG5), respectively. In addition to formula R0 that contains acetyl tributyl citrate (ATBC) as a commercial plasticizer. The mechanical properties, thermal analysis (DSC, TGA) and optical properties of the prepared formulations films were investigated. Theses amphiphilic block copolymers were then applied as plasticizers in different rotogravure ink formulations (F1, F2, F3, F4 and F5) and compared with commercial rotogravure ink formula (F0). The color measurements and optical properties of all formulations were achieved.

It was found that the performance of the prepared copolymers as plasticizers in different formulations based on nitro cellulose resin gives better gloss, adhesion for R1 compared with the other samples and color strength for F1 compared with F0. Finally, all the samples gave excellent plasticizing effect.

The authors believe that type of these materials open the way for a new class of plasticizers that upon application or even degradation gives small ecofriendly molecules (adipic acid and or ethylene glycol moieties) taking into consideration the simplicity of the rout of the synthesis process.

The prepared ecofriendly (PEA-b-PEG)s could be successfully used as plasticizers instead of commercial plasticizer ATBC.

The research provides that the prepared (PEA-b-PEG)s with different molecular weights can act as plasticizers in rotogravure ink formulations, and their performance was acceptable and available.

This paper aims to fabricate a polymer-based polyethylene glycol (PEG) coating with acrylic resin as a binder that can show antiviral activity against the feline coronavirus (FCov) on the glass substrate.

The PEG/acrylic coating systems of different weight percentages were coated on the glass substrates using the spray-coating method and cured at room temperature for 24 h.

The coating system containing 20 Wt.% of PEG exhibits the highest antiviral activities as high as 99.9% against FCov compared with other samples.

Findings will be useful in the development of antiviral coating for PPE fabrics by using the simple synthesis method.

Application of PEG as an antiviral agent in the antiviral coating system with high antiviral activities about 99.9%.

This study aims to synthesize polyethylene glycol (PEG)-rosin derivatives from rosin and PEG for the production of solid soldering fluxes. The PEG-rosin derivatives would be water soluble, and the resulting solid soldering fluxes would have reasonable wetting ability when combined with a low-halide-content activator.

This paper presents a synthetic process for PEG-rosin derivatives. The reaction conditions (including catalyst type, catalyst concentration, reaction temperature and PEG type) were optimized for the synthesis of PEG-rosin derivatives. The chemical and physical properties of PEG-rosin derivatives were characterized by Fourier transform infrared spectroscopy, carbon-13 nuclear magnetic resonance spectrometry, differential scanning calorimetry and gel permeation chromatography. The production and characteristics of water-soluble rosin fluxes (WSRFs) were studied according to the standards of the Japanese Industrial Standards (JIS) Committees.

WSRs were successfully synthesized from rosin and PEG using 2 per cent ZnO as a catalyst, with a 2:1 molar ratio of rosin:PEG at 250°C over 9 h. The resulting WSRs were completely soluble in water. As the PEG3000-rosin had the highest melting point (55.2°C), it was chosen for the preparation of the WSRFs. Activators such as succinic acid, glutaric acid, ethylamine hydrochloride and diethylamine hydrobromide were selected for use in the production of the fluxes. It was found that WSRF 09 and WSRF 04 gave the best performance with the lead-free Sn-0.7Cu solder alloy in terms of good solderability, low halide content (less than 1,500 ppm), high insulation resistance and low corrosion. These fluxes were applied to produce solder pastes with Sn-3.0Ag-0.5Cu alloy and they passed the performance tests as expected for solder paste.

Further studies are necessary on large-scale production and to compare the performance of these fluxes to those from conventional water-soluble fluxes currently available in the market. Application of these fluxes on low-temperature solder alloys such as SnZn and SnBi (Ren et al., 2016) worth further study.

The classification of flux systems according to the JIS 3283 standard does not specify PEG-rosin derivatives in the flux; nevertheless, ranking of the flux systems based on the halide content and corrosion properties of activators would be useful information when selecting flux systems for electronics soldering in water-washable applications. The application of these fluxes in solder paste gave very promising results and is worth investigating into more detail, as well as field test.

This paper aim to comparatively study of mechanical properties of gamma radiation treated raw and polyethylene glycol modified bleached jute reinforced polyester composite. The natural fiber-reinforced composite has been a wide area of research, and it is the preferred choice due to its superior physical and mechanical properties like low density, stiffness and light weight. Among several natural fibers, jute is one that has good potential as reinforcement in polymer composite. Jute fibers biodegradability, low cost and moderate mechanical properties make it as a preferable reinforcement material in the development of polymer matrix composites.

In the present work, raw jute fabrics-reinforced polyester composite (as RJPC) and polyethylene glycol (PEG)-modified bleached jute fabrics-reinforced polyester composite (as MBJPC) were fabricated by the heat-press molding technique at 120°C for 5 min at a pressure of 5 tons. Prior to the composite formulation, low lignin content bleached jute fabrics were chemically modified with PEG for the better compatibility of the fabrics with the polyester matrix and enhancing elongation properties. All the composites irradiated with different gamma radiation dose in the range of 2 to 14 kGy.

The irradiated composites showed highest improved of mechanical properties at the 10 kGy γ-radiation dose. However, the hard and sunlight-sensitive high lignin content γ-RJPC showed higher mechanical properties except elongation properties compared to that of low lignin content γ-MBJPC.

After the γ-ray irradiation, both the γ-RJPC and γ-MBJPC developed high degree of cross-linking among the polyester molecules and thereto fabrics with the consequence of significant changed of surface morphology as observed by atomic force microscopy.

The purpose of this paper is to investigate the effect of polyethylene glycol (PEG), polyvinylpyrrolidone (PVP) and blended formulations on the corrosion inhibition of aluminium in HCl solutions at 30-60°C and to study the mechanism of action.

The inhibitive effect of the homopolymers and polymer blend was assessed using weight loss and hydrogen evolution methods at 30 and 60°C. The morphology of the corroding aluminium surface without and with the additives was visualized using atomic force microscopy. The trend of inhibition efficiency with temperature was used to propose the mechanism of inhibition and type of adsorption.

Results obtained show that inhibition efficiency (η%) increases with increase in concentration of the polymers but decreases with increase in temperature. The inhibition efficiency of the homopolymers and their blends decreased with rise in temperature. Inhibition efficiency was found to be synergistically enhanced on blending the two homopolymers with highest inhibition efficiency obtained for (PEG:PVP) blending ratio of 1:3. The phenomenon of physical adsorption is proposed from the trend of inhibition efficiency with temperature.

The mechanistic aspect of the corrosion inhibition can be better understood using electrochemical studies such as potentiodynamic polarization and electrochemical impedance spectroscopy.

Studies involving the use of polymer blends/mixtures as corrosion inhibitor for metals in corrosive environments are scarce. The results suggest that the mixture could find practical application in corrosion control in aqueous acidic environment. The data obtained would form part of database on the use of polymer–polymer mixtures to control acid-induced corrosion of metal.

The purpose of this paper is to conduct the synthesization of LiFePO₄-C (LFP-C) with fine particle size and enhanced electrochemical performance as the positive electrode material for Li-ion capacitors (LICs) with neutral aqueous electrolyte.

LFP-C was prepared by using polyethylene glycol (PEG) as a grain growth inhibitor, and the effects of the calcination temperature and PEG content on the structure and morphology of LFP-C were investigated. LICs using environment-friendly, safe and low-cost LiNO₃ aqueous electrolyte were assembled with LFP-C as the positive electrode and active carbon as the negative electrode. The electrochemical performances of LFP-C and LICs were studied.

The results show that the particle size of LFP-C decreases significantly through the introduction of PEG. Cyclic voltammetry results show that the LFP-C prepared at 550°C with 1.0 g PEG exhibits the highest C_pe of 725 F/g at the scanning rate of 5 mA/s. Compared to LFP prepared without PEG, the electrochemical performance of optimized LFP-C dramatically increases due to the decrease of the particle size. Moreover, the LIC assembled with the optimized LFP-C exhibits excellent electrochemical performances. The LIC maintains about 91.3 per cent of its initial C_ps after 200 cycles which shows a good cycling performance.

The LFP-C is the suitable positive electrode material for LICs with neutral aqueous electrolyte. LICs can be used in the field of automobiles and can solve the problems of energy shortage and environmental pollution.

Both the LFP-C with fine particle size and its optimal LIC using environment-friendly, safe and low-cost LiNO₃ aqueous electrolyte own good electrochemical performances.

Optimal conditions for condensation of equimolar ratios of stearic acid (St) and polyethylene glycol (PEG) 400, i.e. 180°C, 8hrs and H₂SO₄, 4g/kg (reactants mixture), were utilized to condensate the equimolar ratio of stearic (St), palmitic (Pa) or myristic (My) acid with PEG 300, 400, 600, 2000 or 6000. Each of the fifteen condensates was formed by total conversion (83.5 to 84.1 %). Monoester–diester ratios of the condensates ranged from 4:1 to 49:1. FT – IR spectroscopy and hydrophilic lipohilic balances (HLB) of the condensates were also examined. The condensates had softening and hydrophilic properties of cotton fabric with no yellowing at concentrations of 30 and 50g/l in the presence or absence of DMDHEU (50g/l). The presence of DMDHEU improved the fabric resiliency.

However, the softening and hydrophilic properties of the fabric were inferior in the presence of DMDHEU rather than the absence. In comparison with a commercial softener, PEG 2000- or 6000-based condensates were higher in fabric wettability and pliability but lower in smoothness. Regarding CRA, only My-2000 was comparable to that of the commercial softener in terms of effect.

This study examines solvent extract conductivity (SEC) testing, e.g., Ionograph or Omega Meter testing, which measures ionic cleanliness of printed wiring boards (PWBs). SEC has been a quality control (QC) monitor to assure product electrical reliability. Typical SEC measurements occur after wave soldered products have been solvent‐cleaned. This study concerns SEC testing on new wave soldering processes that involve no solvent cleaning, i.e., inert gas soldering with ‘no clean’ fluxes. Results show ionic residues from ‘no clean’ fluxes may have other characteristics that make QC testing for ionic cleanliness inappropriate. However, SEC may be appropriate as a process control monitor after soldering with these fluxes. An Ionograph measured SEC response for the following chemicals: NaCl, NaF, NaBr, KCl, MgCl2, CaCl2, HCl, succinic acid, malic acid, glutaric acid, adipic acid and ethylene glycol. The list includes inorganic salts, strong electrolytes, which may arise from manufacturing or PWB materials. The list also includes weak organic acids (WOAs) common to ‘no clean’ fluxes. One non‐ionic hygroscopic chemical, ethylene glycol, was studied. Ionograph response was measured via (i) direct injection of aqueous solutions and (ii) immersion of PWBs with individual chemicals as surface deposits. All ionisable compounds, including all WOAs, produced substantial SEC response. Surface conductivity was measured at 35°C/90% relative humidity (RH) with controlled amounts of the above chemicals deposited on clean PWB test circuits. Surface loadings corresponded to the molar‐ionic equivalent of 2.0 ?g/cm2 NaCl. In addition, NaCl, adipic acid and polyethylene glycol (PEG 400) were examined as a function of concentration. Several ionisable chemicals including all WOAs produced no measurable effect, i.e., surface conductivities were indistinguishable on clean and deposited specimens. Surface conductivity increased for ionic contaminants with critical RH below ∼80% and for the non‐ionic hygroscopic glycol. SEC measurements and surface conductivities were compared. The latter is more directly related to electrical reliability. Although all ionic compounds including the WOAs showed a SEC response, not all enhanced surface conductivity. Achievement of critical RH appears to be the important factor. Adipic acid required the presence of hygroscopic glycol to enhance surface conductivity. Therefore, SEC can be a misleading QC test for electrical reliability when WOA flux residues are present.

To amend the efficiency of engineering processes and electronic devices, it is very urgent to assess the irreversibility in the term entropy generation (EG). The efficiency of energy transportation in a system can be improved by minimization of the rate of EG. In this context, the aim of the present study is to estimate irreversible losses of an unsteady magnetohydrodynamic (MHD) flow of a viscous incompressible electrically conducting non-Newtonian molybdenum disulfide-polyethylene glycol Casson nanofluid past a moving vertical plate with slip condition under the influence of Hall current, thermal radiation, internal heat generation/absorption and first-order chemical reaction. Molybdenum disulfide (MoS₂) nanoparticles are dispersed in the base fluid polyethylene glycol (PEG) to make Casson nanofluid. Casson fluid model is considered to characterize the rheology of the non-Newtonian fluid, whereas Rosseland approximation is adopted to simulate the thermal radiative heat flux in the energy equation.

The closed-form solutions are obtained for the model equations by using the Laplace transform method (LTM). Graphs and tables are prepared to examine the impact of pertinent flow parameters on the pertinent flow characteristics. The energy efficiency of the system via the Bejan number is studied extensively.

Analysis reveals that Hall current has diminishing behavior on entropy production of the thermal system. Strengthening of the magnetic field declines the velocity components and prop-ups the rate of EG. Adding nanoparticles into the base fluid reduces the EG, whereas there are an optimum volume fraction of nanoparticles for which the EG is minimized. Further, the rate of decay of EG is prominent in molybdenum disulfide-polyethylene glycol in comparison to PEG.

The results of this study would benefit the industrial sector in achieving the maximum heat transfer at the cost of minimum irreversibilities with an optimal choice of embedded thermophysical parameters. In view of this agenda, this study would be adjuvant in powder technology, polymer dynamics, metallurgical process, manufacturing dynamics of nano-polymers, petroleum industries, chemical industries, magnetic field control of material processing, synthesis of smart polymers, etc.

The novelty of this study is to encompass the analytical solution by using the LTM. Such an exact solution of non-Newtonian fluid flow is rare in the literature. Limited research articles are available in the field of EG analysis during the flow of non-Newtonian nanoliquid subject to a strong magnetic field.

This paper aims to study the physical and chemical characteristics of inkjet titanium dioxide inks for cotton fabric digital printing.

Different dispersing agents through the reaction of glycerol monooleate and toluene diisocyanate were prepared and then performed by using three different polyols (succinic anhydride-modified polyethylene glycol PEG 600, EO/PO Polyether Monoamine and p-chloro aniline Polyether Monoamine), to obtain three different dispersing agents for water-based titanium dioxide inkjet inks. The prepared dispersants were characterized using FTIR to monitor the reaction progress. Then the prepared dispersants were formulated in titanium dioxide inkjet inks formulation and characterized by particle size, dynamic surface tension, transmission electron microscopy, viscosity and zeta potential against commercial dispersants. Also, the study was extended to evaluate the printed polyester by using the prepared inks according to washing and crock fastness.

The obtained results showed that p-chloro aniline Polyether Monoamine (J) and succinic anhydride modified polyethylene glycol PEG 600 (H) dispersants provided optimum performance as compared to commercial standards especially, particle size distribution data while EO/PO Polyether Monoamine based on dispersant was against and then failed with the wettability and dispersion stability tests.

These ink formulations could be used for printing on cotton fabric by DTG technique of printing and can be used for other types of fabrics.

The newly prepared ink formulation for digital textile printing based on synthesized polyurethane prepolymers has the potential to be promising in this type of printing inks, to prevent clogging of nozzles on the printhead and to improve the print quality on the textile fiber.