Surface modification of polyester and polyamide fabrics by low frequency plasma polymerization of acrylic acid

In this study, the surface characteristics of polyester and polyamide fabrics were changed by plasma polymerization technique utilizing acrylic acid as precursor. This monomer was used to produce hydrophilic materials with extended absorbency. The hydrophilicity, total wrinkle recovery angle (WRA°) and breaking strength of the fabrics were determined prior and after plasma polymerization treatment. The modification of surfaces was carried out at low pressure (<100 Pa) and low temperature (<50°C) plasma conditions. The effects of exposure time and discharge power parameters were optimized by comparing properties of the fabrics before and after plasma polymerization treatments. It was shown that two sides of polyester fabric samples were treated equally and homogeneously in plasma reactor. For polyester fabrics, the minimum wetting time, 0.5 s, was observed at two plasma processing parameters of 10 W–45 min and 10 W–20 min, where untreated fabric has a wetting time of 6 s. For polyester fabrics, the maximum value was obtained at 60 W–5 min with the wrinkle recovery angle of 306° where the untreated fabric has 290°. The optimum plasma conditions for polyamide fabrics were determined as 30 W–45 min where 2 s wetting time was observed. Wrinkle recovery angle of untreated polyamide fabric was 264°. In this study, after plasma polymerization of acrylic acid, wrinkle recovery angle values were increased by 13%. No significant change was observed in breaking strength of both fabrics after plasma treatment. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 2318–2322, 2007     

Surface modification of textiles by glow discharge technique: Part II: Low frequency plasma treatment of wool fabrics with acrylic acid

In this study, wool fibers are modified by low frequency plasma polymerization of acrylic acid regarding to its' hydrophobic character due to cuticular cells at their surfaces. Variables of the plasma glow discharge processes were power (40–100 W) and exposure time (5–45 min). The effect of plasma modification in the performance properties of wool were investigated on the basis of hydrophilicity of wool, average wrinkle recovery angle, and breaking strength. The surface chemical structures of fabrics were examined with x‐ray photoelectron spectroscopy. The hydrophobic wool fabric became hydrophilic after all plasma treatments except one (40W–5 min). Average wrinkle recovery angle of the treated fabrics were between 157 and 178°, while that of untreated fabric was 180°. The treated fabrics had a little bit lower angles according to the untreated fabric. However, even the lowest value as 157° means that the fabric has a good crease resistance property. The breaking strengths of fabrics were increased up to 26% after the plasma treatments. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Effects of aging on the adhesive properties of poly(lactic acid) by atmospheric air plasma treatment

The aim of this study was to analyze the durability of a plasma treatment on the surface of poly(lactic acid) (PLA). We used atmospheric‐plasma treatment with air to improve the wettability of PLA by evaluating the aging effect under controlled conditions of relative humidity (RH) and temperature (25% RH and 25°C). We studied the durability of the atmospheric‐plasma treatment by measuring the contact angle, calculating the surface energy, and observing changes in the resistance of the PLA–PLA adhesive bonds. These techniques allowed us to evaluate the hydrophobic recovery phenomenon that the PLA surface suffered as a consequence of the aging process. The results provide the maximum storage time of PLA treated with atmospheric plasma at which the sample retained its good adhesion properties; this time was lower than 3 days under normal atmospheric conditions. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43040.     

Durability study of recycled glass-fiber-reinforced polyamide 66 in a service-related environment

A study of the mechanical properties in an accelerated service-related environment of recycled glass-fiber-reinforced polyamide 66 is reported. Material reinforced with 30 wt % of short fibers was reground and remolded up to seven times. Thermal aging in air at 140°C for up to 3000 h and coolant aging at 110°C for up to 1000 h showed no significant differences in behavior pattern. In addition to mechanical testing, the fiber length measured directly and the matrix stability measured by differential scanning calorimetry (DSC) were used to determine the influence of process-induced degradation on the durability of recycled samples compared with that of virgin samples. The results indicate that fiber length controls the initial properties. The differences in tensile strength and modulus between recycled and virgin samples were similar within the examined times of aging and could be explained by process-induced fiber shortening. The onset of embrittlement during both aging conditions is revealed first in a decrease in tensile elongation at break. Because of a lower degree of fiber reinforcement, the elongation at break of recycled samples was always as good as that of virgin reference samples. However, increasing the number of molding operations up to four to five times resulted in a faster deterioration rate in elongation at break of recycled samples. Further processing had less effect on the deterioration rate. The oxidative stability of the matrix as determined by DSC decreased as a result of repeated processing. The results suggest that matrix stability is related to changes occurring in elongation at break during accelerated aging of samples remolded up to about four times. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65:1631–1641, 1997     

Oil-resistance studies of dynamically vulcanized poly(vinyl chloride)/epoxidized natural rubber thermoplastic elastomer

Dynamically vulcanized poly(vinyl chloride)/epoxidized natural rubber (PVC/ENR) thermoplastic elastomers (TPEs) were prepared with a Brabender plasticorder coupled with a mixing attachment by melt mixing. The blends were prepared at 150°C at a rotor speed of 50 rpm. Curatives concentration was steadily increased from 0 to 1 phr in order to study the vulcanization effect on the plasticized blend. The effectiveness of the dynamic vulcanization was indicated by the Brabender plastograms. The properties investigated include mass swell, tensile strength, elongation at break, modulus at 100% elongation (M100), tear strength, and hardness. The PVC/ENR samples were exposed to two types of environments, namely, air and oil under otherwise identical conditions. The effect of oil and thermooxidative aging on the mechanical properties were characterized at room temperature and 100°C. It was found that at ambient temperature the samples immersed in oil possessed similar properties to those that were exposed to air. Significant enhancement in mechanical properties were observed for both environments at 100°C. This has been attributed to the increase in crosslink density which was manifested by a steady reduction in percent mass swell with increased sulfur loading. The excellent mechanical behavior of the PVC/ENR TPEs even after immersing the samples in oil at 100°C has provided a good indication of the oil resistance of the materials. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 1357–1366, 1998     

Aging studies on flame retardant treated lignocellulosic fibers

The study deals with chemical and flame retardant (FR) treatment of flax fabric. Sheets of flax fabric were subjected to chemical treatments using NaOH and silane coupling agents. A phosphate‐based flame retardant (DAP) was also applied to improve the flammability of the fabric. The effects of the chemical treatments and FR treatments on flax fabric were investigated using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and vertical flame resistance test. Aging studies were carried out by exposing the samples in an environmental chamber at specified conditions for two weeks. The mechanical properties of the fabric, before and after environmental aging, were investigated. Flammability of flax fabric was improved after FR treatment. Thermal studies revealed a shift of decomposition temperature to lower temperatures and an increase in char residue after FR treatment. Despite treatment of the fabric with NaOH and silane, the tensile strength of FR‐treated flax fabric declined by more than 90% after aging for two weeks at 90 °C and 50% RH. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44175.     

聚乙烯纺粘非织造布生产技术初探

采取高温纺丝和较低的侧吹风速度冷却,在聚丙烯(PP)纺粘生产线上生产聚乙烯(PE)纺粘非织造布,探讨了其生产工艺。结果表明:采用熔融指数(每10min)20g的PE为原料,选择纺丝温度250℃,侧吹风速度1.5～1.8m/s,侧吹风温度16～18℃,气流速度5000m/min,生产的PE纺粘非织造布单丝线密度2.16dtex,断裂强度0.68～1.61cN/dtex,断裂伸长率150%～165%。     

XLA包芯纱-棉交织物试织研究

以XLA-棉包芯纱为经纱、纯棉纱为纬纱,在Y002S型小样织机上试织了4种XLA包芯纱-棉交织物,并测试了织物的断裂强力、断裂伸长率、耐磨性和褶皱回复性。测试结果表明:相同经纱密度下,斜纹组织织物的断裂强力和断裂伸长率大于平纹组织的;经纱密度越大,织物的耐磨性和褶皱回复性越好。     

Effect of damp‐heat aging on the structures and properties of ethylene‐vinyl acetate copolymers with different vinyl acetate contents

We reported herein the damp‐heat aging of ethylene‐vinyl acetate copolymers (EVA) with different vinyl acetate (VAc) contents simultaneously for weeks. The aging was carried out under temperature of 40°C and relative humidity of 93% in air atmosphere. The changes of copolymers' structures and properties were investigated by means of FTIR, wide angle X‐ray diffraction (WAXD) and differential scanning calorimetry (DSC) and mechanical tests. CI values derived from ATR‐FTIR spectra have a decrease when aging time is 1 week and then increase during damp‐heat aging process which suggests the first loss then incorporation of O?C group. WAXD infer that the narrowing trend of FWHM and increase of crystal sizes may attribute to the melting and re‐crystallization of secondary crystallization, which is also confirmed by DSC results. Mechanical tests including Shore A and Shore D hardness, modulus at 100%, tensile strength and elongation at break, are all depending on the primary crystallization and influenced little by damp‐heat aging. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effects of prior aging at 288°C in air and in argon environments on creep response of PMR‐15 neat resin

The creep behavior of PMR‐15 neat resin, a polyimide thermoset polymer, aged in air and in argon environments at 288°C for up to 1000 h was evaluated. Creep tests were performed at 288°C at creep stress levels of 10 and 20 MPa. Creep periods of at least 25‐h in duration were followed by 50‐h periods of recovery at zero stress. Prior isothermal aging increased the elastic modulus and significantly decreased the polymer's capacity to accumulate creep strain. The aging environment had little influence on creep and recovery behaviors. However, aging in air dramatically degraded the tensile strength of the material. Dynamic mechanical analysis revealed an increase in the glass transition temperature from ∼330°C to ∼336°C after 1000 h in argon or in air at 288°C. The rise in the glass transition temperature with aging time is attributed to an increase in the crosslink density of the PMR‐15 polyimide. Increase in the crosslink density due to aging in both air and argon environments is likely behind the changes in the elastic modulus and the decreased capacity for inelastic straining. A visibly damaged surface layer of ∼0.16 mm thickness was observed in specimens aged in air for 1000 h. Results indicate that the unoxidized core material governs the overall mechanical response, whereas the oxidized surface layer causes a decrease in tensile strength by acting as a crack initiation site and promoting early failures. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Design and synthesis of organosoluble and transparent polyimides containing bulky substituents and noncoplanar structures

A new diamine monomer, 3,3′‐diisopropyl‐4,4′‐diaminophenyl‐4″‐phenyltouene, was designed, synthesized, and then polymerized with five commercial dianhydrides to obtain a series of novel polyimides via a one‐step method. The obtained polymers showed excellent solubility in most common solvents, even in low‐boiling solvents, such as chloroform, dichloromethane, and tetrahydrofuran. They exhibited a high thermal stability with the glass‐transition temperature in the range 262–318°C and 10% weight loss temperatures in the range 464–488°C under a nitrogen atmospheres. Meanwhile, these polymer films also displayed a high optical transparency with a cutoff wavelength in the range 305–365 nm; prominent mechanical properties with a tensile strength of 65.6–94.9 MPa, a Young's modulus of 1.6–2.8 GPa, and an elongation at break of 9.3–13.7%; a low dielectric constant in the range of 2.91–3.18 at 1 MHz; and an outstanding hydrophobicity with a contact angle above 90.6°. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43266.     

Effect of thermal-oxidative aging on mechanical,chemical, and thermal properties of recycled polyamide 66

This article addresses the effect of thermal aging on unreinforced and glass-reinforced recycled polyamide 66. As an accelerated test, injection-molded test bars were aged at 110, 140, and 170°C for up to 4000 h in air to simulate service life. FTIR spectroscopy demonstrated that the oxidative degradation primarily occurred between the surface and a depth of 0.5 mm. Furthermore, the degradation in the surface region was more pronounced with recycled as well as unstabilized materials. Reprocessing resulted in a faster increase of carbonyl groups, a decrease in melting peak temperature, and elongation at break during subsequent aging. Because of process-induced fiber shortening, however, the elongation at break of recycled reinforced samples was always at least as high as that of virgin samples for up to 4000 h of aging at 140°C. The decrease in melting peak temperature as determined by differential scanning calorimetry (DSC) indicated that the surface or boundary regions of the crystallites in the material are affected by aging. The loss in elongation at break for the reinforced material was shown to correlate with the reduction in melting peak temperature of material taken from the surface region of aged samples. The contribution of the degraded surface region to the properties was studied by removal of surface layers prior to testing. The degradation in the surface region was the sole cause, even of glass fiber-reinforced polyamide, for the embrittlement of aged samples. Furthermore, aging-induced changes in tensile strength and modulus were independent of the removal of the surface region, indicating that these properties are controlled by changes occurring in the bulk of the material. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65:1619–1630, 1997     

Degradation and life prediction of a natural rubber engine mount compound

To assess and predict the functional life of a natural rubber engine mount compound, the mechanical property changes were determined under accelerated aging conditions. The rubber was aged at temperatures ranging from 70 to 110°C for times ranging from 1 h to 5 weeks. Tensile and fatigue measurements were used to characterize the aging trends and mechanisms of the engine mount compound. With the time–temperature superposition approach, the activation energy was found to be about 98 kJ/mol for the elongation at break, 93 kJ/mol for the tensile strength, and 60 kJ/mol for the fatigue life. The tensile strength after aging for 13 weeks at 50°C was predicted to be 18.73 MPa, which was very close to the experimental value of 19.04 ± 2.25 MPa. With a 50% reduction in the tensile strength used as the failure criterion, it was predicted that the tensile strength of the engine mount compound would take 80 days to decrease by 50% at 70°C. At 23°C, it would last approximately 140 times (31 years) its lifetime at 70°C. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Fabrication of continuous nanofiber yarn using novel multi‐nozzle bubble electrospinning

A novel multi‐nozzle bubble electrospinning apparatus, including spinning unit, metering pump, constant flow pump, metal funnel and yarn winder, was designed for the preparation of continuous twisted polyacrylonitrile nanofiber yarns, and the principle of nanofiber yarn spinning was studied. An innovative spinning unit consisting of nozzle and air chamber was used to improve the production of nanofibers. Double conjugate electrospinning was developed using two pairs of oppositely charged spinning units to neutralize the charges. The effects of applied voltage, air flow rate, overall solution flow rate and funnel rotary speed on the fiber diameter, production rate and mechanical properties of the nanofiber yarns were analyzed. Nanofibers could be aggregated stably and bundled continuously, then twisted into nanofiber yarns uniformly at an applied voltage of 34 kV, air flow rate of 1200 mL min^?1 and overall solution flow rate of 32 mL h^?1. With an increase in the funnel rotary speed, the twist angle of the nanofiber yarns gradually increased when the take‐up speed was constant. The yarn tensile strength and elongation at break showed an increasing trend with increasing twist angle. Nanofiber yarns obtained using this novel method could be produced at a rate from 2.189 to 3.227 g h^?1 with yarn diameters ranging from 200 to 386 µm. Nanofiber yarns with a twist angle of 49.7° showed a tensile strength of 0.592 cN dtex^?1 and an elongation at break of 65.7%. © 2013 Society of Chemical Industry     

Surface and adhesion properties of poly(ethylene glycol) on polyester(polyethylene terephthalate) fabric surface: Effect of air‐atmospheric plasma treatment

The surface and adhesion properties of different molecular weight poly(ethylene glycol) (PEG) (400, 1500, and 3000 g/mol) on untreated and air‐atmospheric plasma‐treated PET woven fabrics were studied, with the aim of developing durable hydrophilic PET fibrous structures. PEG application was carried out by padding of the PET fabric in aqueous solution of PEG followed by curing and drying. The surface properties of the PEG‐coated PET fabrics were then characterized using wicking test to measure the water contact angle (θ°) and capillary weight (W_c), and using atomic force microscopy (AFM) images in the tapping mode. Results showed that without a prior air‐atmospheric plasma treatment of the PET fabric, the water contact angle decreased and capillary weight increased with the three PEGs, implying an increase in the hydrophilicity of both inner and outer PET fabric fiber surface. Air‐plasma treatment of the PET fabrics before PEG coating increases further the hydrophilicity of the inner fabric fiber surface: the capillary weight was almost doubled in the case of the three PEGs. Best results were obtained with PEG 1500: water contact angle decreasing from 82° to 51°, and the capillary weight increasing from 11 mg to 134 mg. Moreover, wash fastness test at room temperature and at 80°C confirms improved adhesion of PEG‐1500 to the plasma‐treated PET woven fabric surface, while under the same conditions the plasma‐treated PET without PEG loses completely its hydrophilic character. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

1 100 dtex涤纶帘子线直捻机加捻工艺探讨

采用1 100 dtex涤纶工业丝,在K3501型直捻机上加捻生产涤纶帘子线,锭速8 000 r／min,捻度 440 T／m,外纱张力65％,超喂比5％,防叠角(20±1)°,生产的复捻线断裂强力大于145 N,断裂强力及断裂伸长不匀率均小于1％。同两步法加捻相比,产晶质量和经济效益均明显提高。     

Structure and physical properties of silk fibroin/polyacrylamide blend films

This article deals with the characterization of blend films obtained by mixing silk fibroin (SF) and polyacrylamide (PAAm). The DSC curves of SF/PAAm blend films showed overlapping of the main thermal transitions characteristic of the individual polymers. The exothermic peak at 218°C, assigned to the β‐sheet crystallization of silk fibroin, slightly shifted to a lower temperature by blending. The weight‐retention properties (TG) of the blend films were intermediate between those of the two constituents. The TMA response was indicative of a higher thermal stability of the blend films, even at low PAAm content (≤25%), the final breaking occurring at about 300°C (100°C higher than pure SF film). The peak of dynamic loss modulus of silk fibroin at 193°C gradually shifted to lower temperature in the blend films, suggesting an enhancement of the molecular motion of the fibroin chains induced by the presence of PAAm. Changes in the NH stretching region of silk fibroin were detected by FTIR analysis of blend films. These are attributable to disturbance of the hydrogen bond pattern of silk fibroin and formation of new hydrogen bonds with PAAm. The values of strength and elongation at break of blend films slightly improved at 20–25% PAAm content. A sea–island structure was observed by examining the air surface of the blend films by scanning electron microscopy. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1563–1571, 1999     

气流拉伸聚苯硫醚纤维的制备与表征

对聚苯硫醚(PPS)切片性能进行了研究,利用纺粘无纺布实验机进行了气流拉伸PPS纤维的制备,并对其进行表征。结果表明:PPS切片熔点为280.8℃;在315℃时,PPS熔体流动性最好,熔体流动指数每10 min为158.7 g;PPS纤维直径最细可到30.5μm,随拉伸气流强度增大,纤维断裂强度和取向度都先增大后减小,断裂伸长率则相反,结晶度在小范围内有增大趋势;当拉伸气流强度为40 Hz时,PPS纤维断裂强度达3.28 cN/dtex。     

Effect of hot air aging on the properties of ethylene‐vinyl acetate copolymer and ethylene‐acrylic acid copolymer blends

The aim of this investigation is to evaluate the effect of hot air aging on properties of ethylene‐vinyl acetate copolymer (EVA, 14 wt % vinyl acetate units), ethylene‐acrylic acid copolymer (EAA, 8 wt % acrylic acid units), and their blends. Attenuated total reflection‐Fourier transform infrared spectroscopy, differential scanning calorimeter (DSC), wide angle X‐ray diffraction, and mechanical tests are employed to investigate the changes of copolymer blends' structures and properties. Increase of carbonyl index derived from ATR measurements with aging time suggests the incorporation of oxygen into the polymeric chain. By DSC measurements, the enthalpy at low temperature endothermic peak (T_m2) of EAA becomes less and disappears after 8 weeks aging, but enthalpy at T_m2 of EVA is not influenced by the hot air aging and remains stable despite of the aging time. For various proportions of EAA and EVA blends, enthalpy at T_m2 decreases as the EAA proportion increases when aging time is 8 weeks; after several weeks of hot air aging, the various blends appear a same new peak just over the aging temperature 70°C which is due to the completion of crystals which are not of thermodynamic equilibrium state. Mechanical tests show that increase of crystallinity and hot air aging deterioration both have influence on the hardness, tensile strength, and elongation at break. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

纺丝条件对干纺氨纶性能的影响

通过改变干纺时的纺丝条件并对所得产品的断裂强力、断裂伸长率及均一性进行测试,发现氨纶的断裂强力随着热风的温度升高、风量增大及纺丝速度的提高而增大,断裂伸长率随着风温升高而增大,但随着风量及纺速的增大而减小,双导丝器的使用对于改善氨纶的均一性有利。