Electro-conductive modification of polyethylene terephthalate fabric with nano carbon black and washing fastness improvement by dopamine self-polymerized layer

Modification of textiles with new applications target such as electroconductive fabrics has recently attracted researchers. In this article, carbon black nanoparticles (CB NPs) were applied to polyester fabric through two separate high temperature (HT) exhaustion processing with NaOH and cetyltrimethylammonium bromide (CTAB) as alkali hydrolysis catalyst and dispersing agents. To improve the stability of CB NPs on the fabric a self-polymerized compound, dopamine (DA) was used in a simple dipping method at room temperature for 24 h to form a thin layer of PDA on CB NPs-treated fabric. Field emission scanning electron microscopy (FESEM) was used to study the morphology of the fabrics confirming presence of CB NPs. EDX and mapping patterns showed the percentage and distribution of carbon, nitrogen, and oxygen elements on the fabric surface. The treated fabric indicated an electrical resistance of 14 kΩ turns a LED device on with a 10 V power supply. Self-polymerized DA on the fabric surface led to more nitrogen and oxygen caused higher CB NPs stability. Furthermore, the tensile strength results revealed a 25.8% lower tenacity on the treated fabric. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48035.     

Aqueous reactive polyurethane prepolymer with poly(ethylene oxide) monomethyl ether side chains for the hydrophilic finishing of poly(ethylene terephthalate) fabrics

In this study, a series of aqueous polyurethane (PU) prepolymers were synthesized with 4,4‐methylene bis(isocyanatocyclohexane), poly(ethylene glycol) or polycaprolactone diol (PCL), methyl ethyl ketoxime, and dispersing centers produced by isophorone diisocyanate, N‐diethanol amine, and poly(ethylene oxide) monomethyl ether (PEO), containing different hydrophobic groups (? CH₃ and ? C₆H₄C₉H₁₉) at the end. The thermal properties of the prepolymers and the characteristics of poly(ethylene terephthalate) (PET)‐treated fabrics were investigated. The glass‐transition temperature was the highest in the CC prepolymer containing a benzene ring (? C₆H₄C₉H₁₉) and a long PEO side chain, and it was the lowest in the CA prepolymer having a longer PEO side chain. The CB prepolymer containing a shorter PEO side chain did not produce a melting point of PEO, although a heat endothermic peak of the PCL crystal appeared. The melting point and enthalpy from PEO of the CA prepolymer were larger than those of the CC prepolymer. With respect to the hydrophilic finishing effects of aqueous PU prepolymers for PET fabrics, the fabric treated with the CB prepolymer had higher add‐on and washing durability than the fabrics treated with the CA prepolymer, which was followed by the CC prepolymer with the lowest, but the opposite trend was found for the hydrophilic properties. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

An investigation into surface modification of polyethylene films for hydrophilicity enhancement by catalytic ozonation

For a conventional polyethylene film, ozonation was conducted to increase its surface hydrophilicity. Copper sulfate was found effective as a catalyst in aqueous ozonation to increase the generation of surface peroxides significantly, which is the essential step for hydrophilicity enhancement. The percentage increase in peroxide generation could range from 41% to 58% by aqueous catalytic ozonation over its noncatalyzed gaseous counterpart. The optimum concentration of copper sulfate was found to be 0.05 g/L. After adding the catalyst, the length of ozonation could be significantly reduced so that the bulk mechanical strength of the films, represented by tensile strength, could be well preserved after ozonation. A novel kinetic model for the aqueous ozonation was proposed. This model was developed by combing the reaction mechanism of gaseous ozonation of polyethylene films with that of ozone self‐decomposition in water. The peroxide generation also increased with the applied ozone dose. The surface morphology and contact angle of the film were all examined before and after ozonation. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Polyaniline/poly(ethylene terephthalate) conducting composite fabric with improved fastness to washing

In this article, we report a novel method for the design and development of a polyaniline (PANI)/poly(ethylene terephthalate) (PET) conducting composite fabric based on in situ polymerization. With the aim of improving fabric–PANI adhesion and good fastness to washing, we took some special steps: the alkali reduction pretreatment of the PET fabric before the polymerization of aniline onto the fabric, the introduction of squeezing the laboratory padder on the fabric to push the reagent into the inner part of the fabric, and short immersion time of the aniline‐absorbed fabric in oxidant solution. Factors affecting the conductivity and fastness to washing, including the alkali reduction percentage, the wet pickup of the reagent‐absorbed fabric, the immersion time in oxidant solution, and the reaction time, are discussed. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5775–5780, 2006     

Solid‐state hydrolysis of postconsumer polyethylene terephthalate after plasma treatment

Plasma treatments were applied on the surface of postconsumer polyethylene terephthalate (PET) bottles to increase their wettability and hasten the subsequent hydrolysis process. Sixty‐four treatments were tested by varying plasma composition (oxygen and air), power (25–130 W), pressure (50–200 mTorr), and time (1 and 5 min). The best treatment was the one applied in air plasma at 130 W and 50 mTorr for 5 min, as it provided the lowest contact angle, 9.4°. Samples of PET before and after the optimized plasma condition were subjected to hydrolysis at 205°C. Although the treatment changed only a thin surface layer, its influence was evident up to relatively high conversion rates, as the treated samples presented more than 40% higher conversion rates than the untreated ones after 2 h of reaction. Infrared spectroscopy showed that the terephthalic acid obtained from 99% of depolymerization was similar to the commercial product used in PET synthesis. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

聚对苯二甲酸乙二醇酯的改性及其发泡材料的最新进展

综述了聚对苯二甲酸乙二醇酯(PET)的改性方法及其发泡工艺的研究进展,其中改性方法主要包括固相缩聚、原位共聚和扩链改性,发泡工艺主要有釜压法、模压法、挤出法等.最后,简要介绍了我国PET发泡材料的工业化现状,并指出未来研究和发展的方向.     

Photochemical surface modification of polymers for improved adhesion

A method using photoactivatable reagents is described to modify organic polymer surfaces without changing the bulk properties of the material. The reagents contain a benzophenone or other photoactivatable group which, when exposed to light of appropriate wavelength, generates highly reactive intermediates that covalently bond with nearly any organic material. Some general surface characteristics that can be achieved by this approach, on a wide range of materials, are good wettability, good lubricity, passivation, and priming for either adhesion or immobilization of other molecules. This technology provides tremendous flexibility for tailoring surface characteristics for a broad range of applications. Some materials that have desirable bulk properties for specific applications, however, have surface characteristics that make bonding them to other materials difficult. By photocoupling water-soluble polymers onto the surfaces of such materials, the surface properties can be modified to achieve greatly increased bond strengths with conventional adhesives. For example, using such techniques, the strength of bonding two pieces of high-density polyethylene to each other using a cyanoacrylate adhesive was increased by about 17-fold. Similarly, in preliminary experiments, the bond strengths of silicone rubber to polyvinyl chloride, using cyanoacrylate adhesive, were increased by more than 18-fold. This technology offers great potential for surface modification for improved adhesion.     

Ultraviolet protection of recycled polyethylene terephthalate

Polyethylene terephthalate (PET) is commonly used for food packaging due to its high clarity, high resistance to water vapor, oxygen and carbon dioxide permeation, and good mechanical properties. However, its high transmittance in the ultraviolet‐A (UVA) region leaves food susceptible to UV‐induced degradation reactions. Incorporating post‐consumer recycled (PCR) PET into virgin PET increased UVA absorption 100% when utilizing 100% PCR‐PET, thus, increasing the protection potential of food packaging by reducing UVA‐induced degradation reactions. Comparison of the current data with previous work demonstrated the reproducibility of UVA protection independent of the PC flake source. The thickness‐normalized absorbance at 350 nm was a reliable predictor of the UVA protection potential regardless of composition and manufacture date. Raman, fluorescence, and attenuated total reflectance‐Fourier transform infrared spectroscopy analyses provided support that the UVA absorbing moiety was a quinone derivative formed during degradation reactions that are known to occur during melt processing/re‐processing. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45181.     

Facile fabrication of polyester filament fabric with highly and durable hydrophilic surface by microwave‐assisted glycolysis

Poly(ethylene terephthalate) (PET) fabric with highly and durable hydrophilic surface was fabricated using microwave‐assisted glycolysis. Sodium hydroxide (NaOH) as a catalyst was proven to be suitable for PET glycolysis under assistance of microwave. The modified PET fabric (0.5% NaOH, irradiation 120 s) showed high surface hydrophilicity with a contact angle of 17.4 ° and a wicking length of 19.36 mm. The exposure of the carboxyl‐ and hydroxyl‐end groups on the surface of PET and the introduction of etches were confirmed by Methylene Blue staining and field emission scanning electron microscopy (FESEM), receptively. Although the strength of PET fabric decreased after modification, it was still high enough for textile applications. The thermal properties of the modified PET fabrics were well maintained. The high hydrophilicity and its original properties of PET could be controlled by changing the irradiation time from 60 s to 120 s and adjusting the content of sodium hydroxide from 0.2% to 0.5%. These results suggest microwave‐assisted glycolysis with sodium hydroxide is an effective method for PET hydrophilic finishing. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44069.     

Surface modification of poly(ethylene terephthalate) fibers via controlled radical graft polymerization

Functional chemical modifications on poly(ethylene terephthalate) (PET) fibers via radical graft polymerization could be controlled by managing mutual interactions and affinities between different components in the grafting reaction system. Hansen solubility parameters was used as a tool to quantify affinities of related agents and the polymer, and provided reliable results. The latest results proved the practicality of using Hansen solubility parameters in controlling radical graft polymerizations on surface modifications of PET fibers. Four different monomers with different hydrophilic properties in different solvent and initiator systems were examined, and results confirmed that interactions of initiator‐PET, initiator‐solvent, monomer‐PET, monomer‐solvent, and monomer‐initiator play important roles in determining the grafting reaction efficiency. Results revealed that for the selected grafting systems studied, hydrophilic monomers presented overall favoring affinities toward PET leading to higher grafting yields compared to hydrophobic monomers. The results have instructive impact to commercial applications. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45990.     

Influence of low‐temperature plasma conditions on wicking properties of PA/PU knitted fabric

Plasma surface treatment has been extensively applied in the textile industry for the modification of polymer materials. In this study low‐temperature plasma (LTP) is used for surface treatment of polyamide/polyurethane (PA/PU) knitted fabric. The envisaged plasma effect is an increase in the surface energy of the treated textile, leading toward improved hydrophilic properties. The knitted fabric was treated by LTP using three non polymerizing gases: oxygen, air, and carbon dioxide. After plasma treatment, wettability of samples was tested through their wicking properties measuring capillary rise after water bath contact. The PA/PU knitted fabric samples treated with different plasma gases exhibited different hydrophilic performances. The influence of plasma variables (discharge power, time, pressure) was investigated. Although the chemical characteristics of elastan (PU) and nylon (PA) threads are different, the study has demonstrated that plasma treatment can in the same time alter the surface‐wetting behavior of both the components of the knitted fabric. It was also shown how these treatments can be regulated to produce the desired level of hydrophilicity dependently on the request application. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

Improving the oxygen barrier properties of polyethylene terephthalate by graphite nanoplatelets

Enhancement of the oxygen gas barrier properties of polyethylene terephthalate (PET), used in the packaging industry, is the main objective here. For this purpose, nanocomposites of PET containing graphite nanoplatelets (GNPs) were prepared by melt compounding. The effects of the nanocomposites' structural morphology on oxygen gas permeability were analyzed using a range of thermal, microscopic, and mechanical characterization techniques. The investigated nanocomposite films exhibited GNP exfoliated morphology and good mixing with PET, as well as uniform dispersion within the polymer. All nanocomposite films were shown to possess superior oxygen barrier properties and improved thermal and dimensional stability compared with the plain PET films. In the best case, for 1.5 wt % GNP, the oxygen permeation was reduced by more than 99%. The improved barrier properties are attributed to the direct effect of the GNPs and to their induced increase of degree of crystallinity. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Bonding characteristics of recycled polyethylene terephthalate (PET) fibers coated with maleic anhydride grafted polypropylene in cement‐based composites

In this study, we sought to enhance the bond performance between recycled polyethylene terephthalate(PET) fibers and cement‐based composites using a hydrophilization treatment with hydrophilic maleic anhydride grafted polypropylene (mPP). The bond performance was evaluated with bone‐shaped specimens after the hydrophilization treatment. The effects of the concentration of mPP in the solution in which the PET fibers were immersed (0, 5, 10, 15, and 20%) and the three types of shapes on the surface energy of the recycled PET fibers were evaluated. The pullout behavior, bond strength, and interfacial energy all increased with the concentration of mPP to 15% but decreased at 20%. This occurred because 15% mPP coated the recycled PET fiber thoroughly, whereas a 20% mPP coating resulted in partial cracks, which led to fractures on application of a pullout load. Of the fiber shapes, the embossed fibers demonstrated the best bond behavior. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Impact modification of poly(ethylene terephthalate)

The tensile and impact resistance of impact‐modified poly(ethylene terephthalate) (PET) is investigated. The impact modifiers are polyolefin‐based elastomers or elastomer blends containing glycidyl methacrylate moieties to improve the adhesion with the polyester. The tensile properties are measured on injection molded specimens at room temperature while the Izod impact strength is measured from ?40 to 20°C. The blend morphology is observed by scanning electron microscopy and the dispersed phase average diameter is determined by image analysis. The relation between the impact resistance and the phase morphology is discussed, and the critical ligament size for PET is determined. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2919–2932, 2003     

Butanol alcoholysis reaction of polyethylene terephthalate using acidic ionic liquid as catalyst

The alcoholysis reaction of polyethylene terephthalate (PET) and n‐butanol to produce dibutyl terephthalate (DBTP) and ethylene glycol (EG) was investigated in the presence of a Brönsted–Lewis acidic ionic liquid (IL). It was found that a synergetic effect of Brönsted and Lewis acid sites enhanced the IL catalytic performance, and (3‐sulfonic acid) propyltriethylammonium chlorozincinate [HO₃S‐(CH₂)₃‐NEt₃]Cl‐ZnCl₂ (molar fraction of ZnCl₂ (x) was 0.67) was a good catalyst for the reaction. The conversion of PET was 100%, and the yields of DBTP and EG were 95.3% and 95.7% at 205°C for 8 h, respectively. The reusability of IL was good and after it was used seven times, PET conversion and the yields of DBTP and EG did not significantly decrease. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1840–1844, 2013     

Reactive modification of polyethylene terephthalate with polyepoxides

In attempts to produce modified poldified polyethlene terephthalate (PET) ressins with improved rheology for applications requiring high viscosity and elasticity (e.g., lowdensity extrusion foaming, extrusion blow molding), a novel dimidodiepoxide of low molecular weight was evaluated aschain extender/branching ageent. Its reactivity was compared with that of an ethylene/glycidy1 methacrylate copolymer. The diepoxide showed higher reactivity than the copolymer and could be used at muchlower concentrations. The complex chain extension/degradation reactions occurring in the melt were followed in a batch mixer by torque changes, and by analyzing the prouducts for residual carboxy1 and hydroxy1 content, intrinsic viscosity, insoluble content and melt viscoelastic properties. The perliminary results of this work indicated an overall decrease in carboxy1 content, increase in hydroxy1 content, increase in intrinsic viscosity ans melt viscosity and storage modulus values depending on mixing time and the type and concentration of the additive. It is shown that under certain conditions. reaction of PET with less than 1 wt% diimidodiepoxide may produce materials with rheological characteristics similar to thouse of PET grades that are extrusion foamable by gas injection to low densities.     

Kinetics of hydrolysis of polyethylene terephthalate pellets in nitric acid

The hydrolysis of polyethylene terephthalate (PET) pellets in nitric acid was investigated to determine the kinetic parameters. Experiments were conducted with cylindrical shaped pellets in 13M nitric acid at 80, 90, and 100°C respectively. Also, an experiment was conducted with a waste PET bottle sheet in 9.5M nitric acid at 100°C. The kinetics of the reaction was explained by the shrinking core model with surface chemical reaction as rate controlling step and accounting for surface area reduction due to the deposition of the product terephathalic acid (TPA) on the reaction surface. The activation energy for the reaction was found to be 135 kJ/mol. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87:1781–1783, 2003     

Effect of nanoclay type on dyeability of polyethylene terephthalate/clay nanocomposites

Polyethylene terephthalate (PET)-based nanocomposites containing three differently modified clays were prepared by melt compounding. The influence of type of clay on disperseability, thermal, and dyeing properties of the resultant nanocomposite was investigated by various analytic techniques, namely, X-ray diffraction, optical microscopy (OPM), differential scanning calorimetry, thermal gravimetric analysis, dynamical mechanical thermal analysis, contact angle measurement (CAM), reflectance spectroscopy, and light fastness. OPM images illustrated formation of large-sized spherulites in pure PET, while only small-sized crystals appeared in PET/clay nanocomposites. Decreased glass transition temperatures for all PET/clay nanocomposites indicate that the amorphous regions of such composites become mobile at lower temperatures than those in pure PET. CAMs on the resultant PET composites demonstrated that the wettability of such composites depends on hydrophilicity of the nanoclay particles. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Improving the hydrophilic properties of wool fabrics via corona discharge and hydrogen peroxide treatment

Corona discharge has been widely applied to modify the surfaces of polymers. In this study, corona discharge was combined with a hydrogen peroxide treatment to improve the hydrophilic properties of wool fabric. Scanning electron microscopy photographs showed that the tip of wool scales was etched after corona discharge and that parts of the scales were peeled off after the hydrogen peroxide treatment. The surface hydrophilic properties of the wool fabric were improved greatly by corona discharge. Increases in the discharge voltage and the number of treatment passages enhanced the hydrophilic properties dramatically, but the improved properties deteriorated with increases in the number of washing cycles and storage time. The hydrogen peroxide treatment could improve the hydrophilic properties and especially the wicking properties of the wool fabric. The fabric became weaker and flexible with an average weight loss of 3% after the hydrogen peroxide treatment. A combination of corona discharge treatment and the hydrogen peroxide treatment made the wool fabric absolutely hydrophilic; the water penetration time of the treated fabric was less than 1 s even when the fabric was washed for several cycles or stored for 6 months. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

PET用抗静电剂的研究进展

综述了目前常用于聚对苯二甲酸乙二醇酯（PET）的抗静电剂,如表面活性剂型、亲水性高分子型、纳米材料型,以及其他导电填充材料等的发展现状及研究进展,分析比较了各自的优缺点,并简要介绍了抗静电原理及未来的发展方向。