Cutinase treatment of cotton fabrics

Our study proposes an enzymatic scouring method for cotton fabrics using the enzyme cutinase. We established cutinase treatment conditions for cotton fabrics from their relative activity at different pH levels, temperatures, enzyme concentrations, and treatment times. Weight loss, moisture regain, K/S value, tensile strength, and SEM micrographs of cotton fabrics were analyzed. We determined the optimum cutinase treatment conditions to be as follows: pH of 9.0, temperature of 50°C, cutinase concentration of 100 %, and a treatment duration time of 60 min. We discovered that this cutinase treatment hydrolyzed the cuticle of cotton fabrics. The cutinase treatment did not decrease the moisture regain and the K/S value. The optimum concentrations of Triton X-100 and calcium chloride, which were used as auxiliaries for cutinase treatment, were found to be 0.5 % (v/v) and 70 mM, respectively. Some cracks were observed on the surface of the cotton fibers; however, the tensile strength did not decrease.     

Optimization of enzymatic treatment of polyester fabrics by lipase from <Emphasis Type="Italic">Porcine Pancreas</Emphasis>

The aim of this study was to provide the optimum condition for improving the hydrophilicity of PET fabrics by lipase treatment. The lipase hydrolytic activity, moisture regain, and wettability of PET fabrics were measured at different pH, temperature, reaction time, and concentration. The hydrolytic activity of lipase was evaluated by the number of carboxylic groups, using the titration method. Each treatment condition was controlled by measuring the hydrolytic activity, moisture regain, and wettability. The lipase treatment condition was controlled at pH 7.5, temperature 40 °C, treatment time 90 min, and concentration 6.25 g/l. Lipase treatment was an effective method to improve the moisture regain and wettability of PET fabrics because lipase hydrolysis formed hydrophilic groups on the surface of PET fabrics. The surface of the lipase-treated PET fabrics showed cracks and voids, largely responsible for the increase in the PET’s water-related properties. The nitrogen contents of the lipase-treated PET fabrics were measured at only 0.072 %. Thus, the improvement of the surface wettability of the lipase-treated PET surface was associated with the hydrolytic action of lipase rather than with protein absorption.     

Lipase treatment of polyester fabrics

The aim of this paper is to improve moisture regain of PET fabrics using a lipase treatment. Effects of nine lipase sources, lipase activator and nonionic surfactant on moisture regain of PET fabrics are examined. Moisture regains of lipase-treated samples improve by two times in average compared with untreated and buffer-treated samples. Alkaline treatment creates larger pitting by more aggressive attack into fiber which is proved by SEM and water contact angle measurement. Moisture regain by alkaline treatment (0.568 % ± 0.08) does not improve. However, lipase-treatment (L2 treatment) improves moisture regain up to 2.4 times (1.272 % ± 0.05). Although lipase treatment is more moderate than alkaline treatment, lipase hydrolysis on PET fabrics improves moisture regain, efficiently. K/S values improved confirm that carboxyl and hydroxyl groups are produced on the surface of PET fabrics by lipase hydrolysis. Moisture regain and dyeability improve by lipase hydrolysis on PET fabrics.     

Improvement of hydrophilicity of polylactic acid (PLA) fabrics by means of a proteolytic enzyme from <Emphasis Type="Italic">Bacillus licheniformis</Emphasis>

Polylactic acid (PLA) has received considerable attention as a biomass material for the textile industry. To use a PLA fabric in the textile industry, suitable postprocessing that can promote hydrophilicity of such fabrics is required. Here, hydrolytic action of a proteolytic enzyme (alcalase from Bacillus licheniformis) on PLA fibers was evaluated. In addition, the effects of an additive on the enzymatic hydrolysis were analyzed. The results revealed that the optimal enzymatic-hydrolysis conditions for this alcalase are pH 9.5, temperature 60 °C, enzyme concentration 50 % on weight of fabric (owf), and Lcysteine concentration of 3 mM. PLA fabrics were hydrolyzed effectively, however; there was no damage to these fabrics judging by tensile strength and surface observations. X-ray diffractometry identified a new peak (at 2θ=18.5 °), implying a morphological change caused by the treatment. Moreover, hydrophilic properties such as moisture regain and dyeing properties were enhanced by this proteolytic enzymatic hydrolysis. Therefore, according to this study, enzymatic hydrolysis is a suitable finishing method for improvement of hydrophilicity of PLA fabrics.     

Optimization of papain treatment for improving the hydrophilicity of polyester fabrics

The goal of this study was to establish optimal conditions for improving the hydrophilicity of polyester fabrics. The hydrolytic activity of papain was determined by measuring the number of carboxylic groups in the treatment solution. Papain treatment conditions-such as pH, temperature, treatment time, and enzyme concentration-were optimized by measuring hydrolytic activity, moisture regain, and wettability. Optimal papain treatment conditions were identified as a pH of 7.5, temperature of 30 °C, treatment time of 60 min, and papain concentration of 100 %(o.w.f.). The moisture regain for polyester fabrics treated with papain improved to 1.28±0.02 %, a 2.7-fold increase compared to that of untreated polyester fabrics. As the hydrolytic activity increased, the moisture regain and wettability of the treated fabrics improved. L-cysteine and sodium sulfite did not affect the moisture regain of papain-treated polyester fabrics.     

Optimization of enzymatic treatment of polyamide fabrics by bromelain

In this study, we investigated the effects of enzymatic hydrolysis on polyamide fabrics by using bromelain as an enzyme. The hydrolytic activity of bromelain was evaluated on the basis of the number of carboxylic groups formed on the surface of the polyamide fabrics, and it was measured using the reactive dye absorbance. In addition, 2,4,6-trinitrobenzenesulfonic acid was added as an indicator to measure the number of amino groups released into the treatment liquid by the changes in color of the liquid. The optimum treatment conditions were bromelain pH of 6.0, treatment time of 120 min, temperature of 50 °C, concentration of 10 % (owf), and L-cysteine concentration of 70 mM. The weight loss in the fabric after treatment with bromelain facilitated by L-cysteine significantly improved; however, the tensile strengths of the polyamide fabrics did not show any differences. Bromelain hydrolysis of the polyamide fabrics thus improved hydrophilicity without damaging the fabrics’ strength.     

A new model substrate for cutinase hydrolyzing polyethylene terephthalate

This study aimed at comparatively investigating the enzymatic hydrolysis of a new model substrate water-soluble polyester (WSP) and polyethylene terephthalate (PET) with cutinase. The changes of WSP solution properties were investigated by measuring pH value, alkali consumption, and specific viscosity. The results indicated that pH value of enzymatically treated WSP solution was decreased, causing an increase in alkali consumption. The decreases in specific viscosity and the glass transition temperature (T _g ) of WSP treated with cutinase indicate the decrease in its molecular weight as demonstrated in gel permeation chromatography analysis (GPC). Cutinase treatment resulted in an improvement of the hydrophilicity of PET fabrics, which was determined by dye uptake and water contact angle.     

Development of superhydrophobic polyester fabrics using alkaline hydrolysis and coating with fluorinated polymers

Alkaline hydrolysis is one of the most classic fiber finishing methods, however, its potential as tuning surface superhydrophobicity in mass scale has not been studied much. In this research, fine roughness was formed on the polyester fiber surfaces by alkaline hydrolysis at room temperature and fluorinated polymer mixtures were further coated. The developed superhydrophobic fabrics were evaluated in terms of structural changes, mechanical properties, surface hydrophobicity, and permeability for practical applications. As alkaline hydrolysis treatment time increased, surface roughness was increased as a lot of nano-craters were generated with the decrease of fabrics weight and tensile strength as well. As air pockets formed through nano-craters on the fiber surfaces, static contact angle increased, and shedding angle tended to decrease. In this study, the sample treated with alkaline hydrolysis for 20 minutes showed the highest static contact angle of 167.8±1.3° and lowest shedding angle of 4.4±2.3°. Considering tensile strength loss, however, the 15-minute alkaline hydrolyzed fabrics which showed static contact angle of 162.2±2.7° and shedding angle of 8.8±0.2° was selected as the optimal condition for practical application. The newly developed superhydrophobic fabrics were found to have higher water vapor and air permeability than those of untreated samples. At the same time, fluoropolymer coating played a certain role for tensile strength and water vapor permeability demonstrating the importance of understanding and designing proper fluorinated-compound treatment processes.     

The combined use of cutinase,keratinase and protease treatments for wool bio-antifelting

A combined treatment method of cutinase, keratinase, and protease was applied in the wool processing to modify the wool properties. The results demonstrated that individual protease treatment did not obviously improve the wettability and anti-felting property of wool fabrics. The combined process of cutinase and protease seemed more efficient than the keratinase-protease method, the obtained wettability and anti-felting ability of wool fabric were more encouraging. The combined use of cutinase, keratinase, and protease treatments endowed wool with more satisfactory properties compared to other methods. The contact angle of the protease-treated wool fabric reduced to 66 ° and the area shrinkage decreased to 5.2 % with an acceptable strength loss of 14 %. Reaction mechanism of the three-step enzymatic process was proposed in this paper. The data from amino acid analysis revealed the cooperative actions of cutinase, keratinase, and protease treatments during the combined enzymatic processing.     

Environmentally benign alternatives: Plasma and enzymes to improve moisture management properties of knitted PET fabrics

Effects of enzymatic and atmospheric plasma treatments individually and their combinations on knitted PET fabrics were investigated in terms of hydrophilicity, surface modification and moisture management properties. Cutinase from Humicola Insolens, lipase from Candida SP and atmospheric plasma with air and argon gases were applied to PET fabrics. To evaluate results, moisture management tester (MMT) and scanning electron microscopy (SEM) were utilized. Wicking heights of samples were measured by wicking test method. Improved moisture management properties were observed with environmentally benign processes compared to the untreated ones. Especially combined treatments have given the same or slightly better results than those of conventional alkaline treatments. Fabrics treated with plasma and then followed by enzymatic incubations have significantly improved the wetting time, absorption rates and spreading speed results.     

Dyeing and fastness properties of a reactive disperse dye on PET, nylon, silk and N/P fabrics

Dyeing and color fastness properties of a reactive disperse dye containing an acetoxyethylsulphone group on PET, Nylon, silk and N/P fabrics were examined. The reactive disperse dye exhibited almost the same dyeing properties on PET fabric as a conventional disperse dye except the level of dye uptake. The most appropriate pH and dyeing temperature for the dyeing of Nylon fabric were 7 and 100°C respectively. The build-up on Nylon fabric was good and various color fastnesses were good to excellent due to the formation of the covalent bond. Application of the reactive disperse dye on silk fabric at pH 9 and 80°C yielded optimum color strength. The rate of dyeing on Nylon fabric was faster than that on PET fabric when both fabrics were dyed simultaneously in a dye bath, accordingly color strength of the dyed Nylon was higher. The reactive disperse dye can be applied for one-step and one-bath dyeing of N/P mixture fabric with good color fastness.     

Helium/oxygen atmospheric pressure plasma treatment on poly(ethylene terephthalate) and poly(trimethylene terephthalate) knitted fabrics: Comparison of low-stress mechanical/surface chemical properties

Helium-oxygen plasma treatments were conducted to modify poly(trimethylene terephthalate)(PTT) and poly(ethylene terephthalate) (PET) warp knitted fabrics under atmospheric pressure. Lubricant and contamination removals by plasma etching effect were examined by weight loss (%) measurements and scanning electron microscopy (SEM) analysis. Surface oxidation by plasma treatments was revealed by x-ray photoelectron spectroscopy (XPS) analyses, resulting in formation of hydrophilic groups and moisture regain (%) enhancement. Low-stress mechanical properties (evaluated by Kawabata evaluation system) and bulk properties (air permeability and bust strength) were enhanced by plasma treatment. Increasing interfiber and interyarn frictions might play important roles in enhancing surface property changes by plasma etching effect, and then changing low-stress mechanical properties and bulk properties for both fabrics.     

Dyeing properties of nylon,PET, and N/P mixture fabric with reactive-disperse dyes having a sulfatoethylsulfone group

The dyeing and color fastness properties of two reactive-disperse dyes containing a sulfatoethylsulfone group on nylon, PET and N/P mixture fabrics were examined. The rate of dyeing on nylon fabric was greatly dependent upon dye bath pH. The final dye uptakes at all pH, however, were as high as 97 %. Color strength of the dyed nylon fabric linearly increased up to 0.5 %owf and then slowed down over 1 %owf dyeing. Washing and rubbing fastness of the dyed nylon fabric were excellent, but grade of light fastness was moderate. Dyeability of the reactive-disperse dyes on PET fabric was not much affected by pH, and K/S values of PET fabric dyed at pH 5–8 were lower than those of nylon fabric at all pH examined. Buildup and color fastnesses properties on PET fabric showed the same tendency with nylon fabric. The rate of dyeing of the reactive-disperse dyes on nylon fabric was faster than on PET fabric when both fabrics were dyed simultaneously in the same dye pot, resulting in higher color strength of nylon than PET. The reactive-disperse dyes were found to be adequate to the one-bath, one-step dyeing of N/P mixture fabric when applied at pH 5 and 120 °C.     

Effect of mercerization on mechanical, thermal and degradation characteristics of jute fabric-reinforced polypropylene composites

Jute fabric reinforced polypropylene composites were fabricated by compression molding technique. Fiber content in the composites was optimized at 45 % by weight of fiber by evaluating the mechanical parameters such as tensile strength, tensile modulus, bending strength, bending modulus. Surface treatment of jute fabrics was carried out by mercerizing jute fabrics with aqueous solutions of NaOH (5, 10 and 20 %) at different soaking times (30, 60 and 90 mins) and temperatures (0, 30 and 70 °C). The effect of mercerization on weight and dimension of jute fabrics was studied. Mechanical properties of mercerized jute-PP composites were measured and found highest at 20 % NaOH at 0 °C for 60 min soaking time. Thermal analytical data from thermogravimetric and differential thermal analysis showed that mercerized jute-PP composite achieved higher thermal stability compared to PP, jute fabrics and control composite. Degradation characteristics of the composites were studied in soil, water and simulated weathering conditions. Water uptake of the composites was also investigated.     

Sound absorbent,flame retardant warp knitting spacer fabrics: Manufacturing techniques and characterization evaluations

This study proposes a combination for reciprocal reinforcement between warp knitting spacer fabrics and PU foams. PET/Kevlar nonwoven fabrics are made with an 80:20 ratio and an incorporation of various needle-punching speed of 100, 150, 200, 250, and 300 needles/min. Ascribing to having an optimal bursting strength, sound absorption coefficient, and limited oxygen index (LOI), the PET/Kevlar nonwoven fabric that is made by 200 needles/min are selected to be combined with a glass-fiber fabric by applying needle punch in order to form a surface layer. Next, warp knitting spacer fabrics and the nonwoven fabrics are laminated, followed by being combined with polyurethane (PU) foam that are featured with different densities of 200, 210, 220, 230, and 240 kg/m³ in order to form spacer fabric/PU foam composites with multiple functions. The composites are then tested with a drop-weight test, a compression test, a bursting strength test, a sound absorption test, and a horizontal burning test. The test results indicate that all spacer fabric/PU foam composites reach a horizontal burning level of HF1, and their sound absorption coefficients at 2500-4000 Hz also suggest a satisfactory sound absorption. In particular, the optimal residual stress and compressive strength are present when the composites contain 210 kg/m³ PU foam. Similarly, the optimal bursting strength of the composites occurs when they are composed of 230 kg/m³ PU foam. The spacer fabric/PU foam composites are proven to have high strengths, sound absorption, and fire retardant, and thus have promising potentials for use as construction materials and light weight composite planks.     

Structural Transformation and Dyeing Performance of Poly(Ethylene Terephthalate) Filament Using Dicationic Imidazolium Ionic Liquid

3,3'-[1,2-ethanediylbis (oxy-2,1-ethanediyl)]-bis[1-methyl-imidazolium]-dibromide (DImDBr), a gemini imidazolium ionic liquid, was synthesized for the modification and dyeing promotion of poly(ethylene terephthalate) (PET) filaments. The results showed that parameters such as treatment temperature, time, and DImDBr concentration played a critical role on the tensile strength and tensile strength retention of modified PET filaments. The optimal treatment parameters of the PET filaments were 120 °C for 90 min with addition of 6 % ionic liquid. The influence of disperse dyeing parameters (temperature, time, and dye concentration) on DImDBr modified PET filaments were also studied. The disperse dyed PET filaments (after treatment with DImDBr) exhibited a desirable color strength (K/S value), excellent soap washing fastness, light fastness, and rubbing fastness. Furthermore, the native PET filaments and DImDBr treated PET filaments were characterized by FT-IR, XRD, DSC, TGA, and SEM. Density functional theory (DFT) simulation showed the presence of two kinds of hydrogen bonds (C-H/O and O-H/Br) and eight strong hydrogen bonds in the DImDBr/cis-PET monomers, while only three hydrogen bonds were found in the DImDBr/trans-PET monomers. The structural transformation from the crystalline phase to the amorphous phase (FT-IR, XRD, and DFT simulation) after DImDBr modification confirmed the dyeing promotion of PET filaments at lower temperature.     

The effect of a new setting agent for wool

Pleated wool fabrics were prepared by the treatment with ethylenediamine (EDA) at 90°C for 30 min. The degree of set, tensile property and dyeing of the treated fabrics have been discussed in relation to the concentration of EDA in the treatment system. No significant decreases in tensile strength and elongation, and great increases of exhaustion of synthetic and natural dyes were observed. Pleat and flat set were successfully attained in a wide range of the concentration of EDA. Excellent dyeability and setability of the fabrics obtained were considered to be associated with the existence of new crosslink, β-N-(2-aminoethyl)alanino-β-aminoalanine and the pendant group, β-N-(2-aminoethyl) aminoalanine produced by the reaction of EDA with dehydroalanine intermediate.     

Development of moisture transition ability on porous complex structured woven fabric with convergence of pattern,porosity, and plasma technology

A porous complex structured woven fabric was manufactured to maximize the moisture transition ability of the prepared fabric by increasing the absorptive property of the fabric through surface modification using plasma, which is a dry modification method. Porous single and complex structured woven fabrics were produced by applying pattern, porosity, and plasma technology, including fabric patterning based on the sheath/core complex structure, the formation of porosity by removing the weft thread or warp thread, and hydrophilic surface treatment using plasma and the improvement in water absorption of different fabrics by the porous and plasma treatment was investigated. Therefore, two different types of fabrics were prepared. One is the porous single structured FAB-SINGLE fabric which was taken out in the direction of the Polyester (PET) warp thread of a general single structure to form a porous. Another is FAB-COMPLEX fabrics that the water-soluble polylactic acid (PLA) yarns with a 1.7 to 2.0 times longer absorption distance than that of PET yarns were inserted into the weft threads, and the PLA yarns were dissolved in a solvent to form the porous complex fabric. And then the physical properties and water absorption of the two types of fabric were compared after the plasma treatment. The results showed that when the FAB-SINGLE fabric, which has porosity induced by the removal of the warp threads in a certain gap, was plasma treated for 5 min, the contact angle was decreased to the extent that a measurement of the contact angle was impossible, whereas the fabric that had not undergone a plasma treatment had a contact angle of 123.6 o. The contact angle of the FABCOMPLEX with porosity caused by the dissolution of the PLA yarns was reduced from 76.8 o to 0 o after 3 minutes of a lowtemperature plasma treatment, indicating that the hydrophilic property was increased. In addition, the water absorption measurements showed that the absorption height was increased from 2.3 cm of the fabric sample that had not been treated with plasma to the highest absorption height of 8.3 cm, suggesting that the water absorption also increased with the improvements in moisture transition ability by the plasma treatment. The physical tensile strength of the fabrics was not changed by the plasma treatment, despite the changes on the fabric surface, suggesting that the combination of double complex structures and the plasma treatment helped improve the water absorption.     

Effectiveness of flavourzyme treatment on polyamide fabric

We characterized the effectiveness of Flavourzyme treatment in the hydrolysis of amide bonds in polyamide fabric by quantitating the ionic groups released into the treatment liquid and those formed on the fabric surface. On the basis of hydrolytic activity, we demonstrated that Flavourzyme effectively hydrolyzed amide bonds in polyamide (PA) fabric. The optimal treatment conditions were found to be pH 7.0, temperature 40 °C, treatment time 120 min, and Flavourzyme concentration 10 % based on weight of fiber. PA fabric treated with Flavourzyme exhibited increased numbers of amino and carboxyl groups, as evaluated by zeta potential and color strength. As the amounts of ionic groups formed by Flavourzyme hydrolysis increased, the water contact angle and water absorbency time decreased.     

A study of physical modification on grey cotton by laser irradiation

The surface morphology of the CO₂ laser treated grey cotton fabrics was studied which showed a characteristics sponge-like structure on cotton fibres after treating with CO₂ laser irradiation. The laser treatment parameters ranging from 100 to 150 pixel time and 40 to 70 dot per inch (dpi) were irradiated on the grey cotton fabrics directly and the degree of physical modifications, such as surface morphology, wettability and fabric strength, were changed accordingly with various laser treatment parameters. The surface morphology, wettability and tensile strength of cotton fibre treating with laser were evaluated using different instruments, such as Scanning Electron Microscope (SEM), contact angle meter and tensile strength machine. In spite of creating a sponge-like structure on fibre surface after treating with laser, the wettability of the samples was highly improved but the tensile strength was decreased.