Surface modification of polyester fabrics by enzyme treatment

In this study, the effect of enzymatic hydrolysis using lipase and cutinase on poly(ethyleneterephthalate) (PET) fabrics was investigated in an attempt to improve the hydrophilicity of these fabrics. The hydrolytic activity of the enzymes was expressed for variations in pH levels, temperatures, enzyme concentrations, and treatment times. The effects of using a nonionic surfactant were examined by measuring moisture regain and surface wettability. Finally, the fabric characteristics that were affected by enzyme treatment were evaluated by tensile strength and scanning electron microscopy. The optimal treatment conditions for lipase were determined to be a pH of 4.2, a temperature of 50 °C, a lipase concentration of 100 %, and a treatment time of 90 min; those for cutinase were determined to be a pH of 9.0, a temperature of 50 °C, a cutinase concentration of 100 %, and a treatment time of 60 min. At optimal enzymatic treatment conditions, we got the significant results of increase on the moisture regain and the water contact angle (WCA) and water absorbency effectively decreased. Triton X-100 facilitated cutinase hydrolysis on PET fabrics; however, it was ineffective for lipase. With enzymatic treatment, the tensile strength did not decrease.     

Pervaporation separation of dimethyl carbonate/methanol binary mixtures with poly(vinyl alcohol)-perfluorslulfonic acid/poly(acrylonitrile) hollow fiber composite membranes

Using poly(vinyl alcohol) (PVA) and perfluorslulfonic acid (PFSA) as coating materials, poly(acrylonitrile) (PAN) hollow fiber ultrafiltration membrane as substrate, PVA-PFSA/PAN composite membranes were fabricated by dip-coating method. The fabricated composite membranes were used to the separation of dimethyl carbonate (DMC)/methanol (MeOH) binary mixtures by pervaporation process. SEM images verify that the coated layer is well combined with substrate and the thickness nearly linearly increases with the coating solution concentration. The separation factor increases but at cost of the decline of permeation flux when the concentration of the coating solution or its PVA mass fraction increase. The permeation flux increases and separation factor slightly increases with the feed temperature increasing at 30–60 °C. The increase of feed MeOH concentration leads to an improvement of permeation flux and a decline of separation factor.     

Microwave-mediated rapid tailoring of PET fabric surface by using environmentally-benign,biodegradable Urea-Choline chloride Deep eutectic solvent

Deep eutectic solvent, urea-choline chloride (URC), was used to control surface of poly(ethylene terephthalate) (PET) fabric under microwave irradiation with or without sodium hydroxide (NaOH) for hydrophilic-hydrophobic properties. Wicking and contact angle evaluations indicated that the URC-treated PET fabric drastically changed its surface characteristics from highly hydrophobic to highly hydrophilic (or vice versa) by carefully adjusting alkali concentration and microwave irradiation time. For instance, an instant wicking was achieved on URC-treated PET with 1 % NaOH at 60 s of microwave irradiation, whereas highly hydrophobic PET surface with 2600 s wicking time and 135.6 ° contact angle was acquired by adding 5 % NaOH at the same microwave irradiation. Methylene Blue staining and FTIR analyses suggested that a minimal hydrolysis occurred through URC-treatment with NaOH under microwave irradiation and hydrophilicity was mainly achieved by physical disruption of the fiber. The treated fabrics were further analyzed by DSC, TGA, and SEM. Therefore, a rapid control of hydrophilic-hydrophobic surface of PET fabric was achieved with a little side reaction by using environmentally-benign, biodegradable URC deep eutectic solvent.     

Synthesis,analysis and simulation of carbonized electrospun nanofibers infused carbon prepreg composites for improved mechanical and thermal properties

This paper reports the fabrication, characterization and simulation of electrospun polyacrylonitrile (PAN) nanofibers into pre-impregnated (prepreg) carbon fiber composites for different industrial applications. The electrospun PAN nanofibers were stabilized in air at 270 °C for one hour and then carbonized at 950 °C in an inert atmosphere (argon) for another hour before placing on the prepreg composites as top layers. The prepreg carbon fibers and carbonized PAN nanofibers were cured together following the prepreg composite curing cycles. Energy dispersive X-ray spectroscopy (EDX) was carried out to investigate the chemical compositions and elemental distribution of the carbonized PAN nanofibers. The EDX results revealed that the carbon weight % of approximately 66 (atomic % 72) was achieved in the PAN-derived carbon nanofibers along with nitrogen and lower amounts of nickel, oxygen and other impurities. Thermomechanical analysis (TMA) exhibited the glass transition regions in the prepreg nanocomposites and the significant dependence of coefficient of thermal expansion on the fiber directions. The highest value of coefficient of thermal expansion was observed in the temperature range of 118-139 °C (7.5×10^-8 1/°C) for 0 degree nanocomposite scheme. The highest value of coefficient of thermal expansion was observed in the temperature range of 50-80 °C (37.5×10^-6 1/°C) for 90 degree nanocomposite scheme. The test results were simulated using ANSYS software. The test results may be useful for the development of structural health monitoring of various composite materials for aircraft and wind turbine applications.     

Heat resistance,impact strength,and transparency of PET copolymer containing fluorenylidene bis(2-phenoxyethanol)

Poly(ethylene terephthalate) (PET) copolymers containing fluorenylidene bis(2-phenoxyethanol) (FBPE) were prepared. The glass transition temperature of copolymers increased continuously with the composition of FBPE. The glass transition temperature of PET/FBPE copolymer at loading of 15 mol% FBPE was 107 °C, which was 35 °C higher than that of PET. The melting temperature of PET/FBPE copolymers was decreased with the composition of FBPE, and it disappeared above 6 mol% of FBPE. The heat deflection temperature of copolymers increased from 60.7 °C for PET to 89.9 °C for the copolymer containing 15 mol% of FBPE. The values of optical transmittance of copolymers were 89-90 % at 550 nm, and no significant change was observed with the FBPE composition. The impact strength value of copolymer at loading of 10 mol% FBPE was 26 J/m, which was 20 J/m higher than that of PET.     

Superhydrophobic PET fabrics achieved by silica nanoparticles and water-repellent agent

We report herein a superhyrodrophobic poly(ethylene terephthalate) (PET) fabric prepared through a biomimetic method of the Lotus effect. To attain the Lotus effect on the PET fabrics, physical roughness and chemical hydrophobicity were controlled by adopting silica nanoparticles and a commercial water-repellent agent, respectively. For this, narrow-size distributed silica nano-particles were prepared by a sol-gel process. The water contact angle on PET fabric treated with both silica nanoparticles and water-repellent agent reached 158°, which was much higher than 137° reached by the fabric treated with the water-repellent agent only.     

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.     

Influence of storage temperature on rate of potato tuber tissue infection caused byPhytophthora infestans (mont.) de bary estimated by digital image analysis

Summary Potato tubers were inoculated with two biotypes ofPhytophthora infestans then stored at 3,7, 10 and 15°C. Image analysis quantified average reflective intensity (ARI) of diseased tissue from cut surfaces of sample tubers. Tuber tissue infection and infection rate were measured by calculating Mean ARI of samples. Average tuber tissue infection and infection rate was minimal at 3°C (P.i.-US8 orP.i.-US1). Tuber tissue infection increased at temperatures >3°C, from 220 Mean ARI seven days after inoculation (dai) to 190–150 Mean ARI 50 dai (depending on cultivar and biotype ofP. infestans). Rate of tuber tissue infection caused byP.i.-US1 at 7°C was about zero in cv. Snowden but greater than −0.2 ARI day⁻¹ (cvs Russet Burbank and Superior). Rate of late blight infection in tuber tissue generally increased with temperature from −0.2 ARI day⁻¹ (at 7°C) in all cultivars to a maximum of −0.8 ARI day⁻¹ (10°C).     

Acrylamide/potassium 3-sulfopropyl methacrylate/sodium alginate/bentonite hybrid hydrogels: Synthesis,characterization and its application in lauths violet removal from aqueous solutions

In this report, it was to investigate that the swelling and dye sorption properties of a series of novel hybrid composite hydrogel sorbent systems containing polysaccharide/clay polyelectrolyte based on acrylamide/potassium 3-sulfopropyl methacrylate and sodium alginate, and clay such as bentonite were synthesized with free radical solution polymerization by using ammonium persulfate/N,N,N’,N’-tetramethylethylenediamine as redox initiating pair in presence of poly(ethylene glycol) diacrylate as a crosslinker. Swelling experiments were performed in water at 25 °C, gravimetrically. The hydrogels, the semi-interpenetrating polymer networks, and the hybrid composite hydrogel systems that synthesized in this study have showed high water absorbency. Some swelling and diffusion properties were calculated, and they were discussed for the hybrid hydrogel systems prepared under various formulations. The equilibrium percentage swelling degree of highly swollen hybrid composite hydrogel systems ranges are 718-2055 %. FT-IR analysis and SEM technique were applied for characterization. For sorption of water-soluble cationic dye such as lauths violet into the hydrogel systems was studied by batch sorption technique at 25 °C. For equilibrium sorption studies, dye sorption percentage, dye uptake performance, and partition coefficient of the hydrogel systems have been investigated. The values of dye sorption percentage of the hydrogels were changed among 87.11-96.39 %. Consequently, the hydrogel systems developed in this study could serve as a potential device for water and dye sorbent.     

Functinalization of poly(ethylene terephthalate) fibers by grafting of maleic acid/methacrylamide monomer mixture

Functionalized poly(ethylene terephthalate) (PET) fibers were synthesized by grafting of maleic acidmethacrylamide (MAA-MAAm) monomer mixtures by using benzoylperoxide as initiator onto PET fibers in an aqueous medium. The functionalized fibers were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimeter, and scanning electron microscopy. The effects of reaction conditions, such as monomer mixture ratio, monomer mixture and initiator concentration, polymerization time, and temperature on grafting were investigated. In alone grafting of MAA, grafting was not observed. However, the use of MAAm as a comonomer increased the amount of MAA inserted to the PET fiber up to 40.7 %. An increase in the temperature between 75 and 95 °C and also, increase in monomer mixture concentration between 0.50 and 1.00 M increased the grafting rate and saturation graft yield. The graft yield has shown an increase up to an initiator concentration of 1.0×10⁻² M and decreased afterwards. The grafting increased the dyeability with disperse, acidic and basic dyes, and water absorption capacity but decreased the thermal stability of the fibers.     

Thermal and mechanical properties of modified CaCO3 filled poly (ethylene terephthalate) nanocomposites

Poly(ethylene terephthalate) (PET)/CaCO₃ and PET/modified-CaCO₃ (m-CaCO₃) nanocomposites were prepared by melt blending. The morphology indicated that m-CaCO₃ produced by reacting sodium oxalate and calcium chloride, was well dispersed in PET matrix and showed good interfacial interaction with PET compared to CaCO₃. No significant differences in the thermal properties such as, glass transition, melting and degradation temperatures, of the nanocomposites were observed. The thermal shrinkage of PET at 120 °C was 10.8 %, while those of PET/CaCO₃ and PET/m-CaCO₃ nanocomposites were 2.9–5.2 % and 1.2–2.8 %, respectively depending on filler content. The tensile strength of PET/CaCO₃ nanocomposite decreased with CaCO₃ loading, whereas that of PET/m-CaCO₃ nanocomposites at 0.5 wt% loading showed a 17 % improvement as compared to neat PET. The storage modulus at 120 °C increased from 1660 MPa for PET to 2350 MPa for PET/CaCO₃ nanocomposite at 3 wt% loading, and 3230 MPa for PET/m-CaCO₃ nanocomposite at 1 wt% loading.     

Electrospun form-stable phase change composite nanofibers consisting of capric acid-based binary fatty acid eutectics and polyethylene terephthalate

The four binary fatty acid eutectics of capric-lauric acid (CA-LA), capric-myristic acid (CA-MA), capric-palmitic acid (CA-PA), and capric-stearic acid (CA-SA) were firstly prepared as solid-liquid phase change materials (PCMs); then, the composite phase change nanofibers consisting of CA-based binary fatty acid eutectic and polyethylene terephthalate (PET) were fabricated by electrospinning for thermal energy storage. The maximum mass ratios of fatty acid eutectics versus PET in the nanofibers could reach up to 2/1. The FE-SEM images revealed that the composite nanofibers possessed smooth and cylindrical morphological structure having diameters of about 100–300 nm. The fatty acid eutectic could be uniformly distributed in the three-dimension network structure of the PET nanofibers. The FT-IR results indicated that the fatty acid eutectic and PET had no chemical reaction and exhibited good compatibility with each other. The DSC measurements showed that the prepared composite nanofibers had appropriate phase transition temperatures (about 5–38 °C) based upon climatic requirement, whilst the phase change temperatures and the enthalpy values of the composite nanofibers could be adjusted by changing the contents and the types of binary fatty acid eutectics in the nanofibers. The TGA results suggested that the onset thermal degradation temperatures and charred residues at 700 °C of the composite nanofibers were lower than those of pure PET nanofibers, but higher than those of fatty acid eutectic, which were caused by the fact that the PET had better thermal stability than fatty acid eutectic.     

Copolymerization of benzyl methacrylate and a methacrylate bearing benzophenoxy and hydroxyl side groups: Monomer reactivity ratios,thermal studies and dielectric measurements

Statistical copolymers of 2-hydroxy-3-benzophenoxy propyl methacrylate (HBPPMA) and benzyl methacrylate (BzMA) in different feed ratios were synthesized by free radical copolymerization method at 60 °C in presence of AIBN initiator. The compositions of copolymer were estimated from ¹H-NMR technique. The monomer reactivity ratios of HBPPMA and BzMA were calculated as r₁ (r_HBPPMA)=0.51±0.076 and r₂ (r_BzMA)=1.07±0.140 for Kelen-Tüdos method, and was estimated as r₁=0.37±0.0006 and r₂=0.64±0.0485 according to Fineman Ross equation. The average values estimated from the two methods showed that monomer reactivity ratio of benzyl methacrylate was a slightly high in comparison to HBPPMA. The copolymer system showed an azeotropic point, which is equal to M _BzMA =m _BzMA =0.43. DSC measurements showed that the T_g’s of poly(HBPPMA) and poly(BzMA) were 84 °C and 73 °C, respectively. The T_g in the copolymer system decreased with increase in benzyl methacrylate content. The decomposition temperature of poly(BzMA) and poly(HBPPMA) occurs in a single stage at about 207 °C and 260 °C, respectively. Those of HBPPMA-BzMA copolymer systems are between decomposition temperatures of two homopolymers. The dielectric constant, dielectric loss factor and electrical conductivity were investigated depend on the frequency of the copolymers. The highest dielectric constants depending on all the studied frequencies were recorded for the poly(HBPPMA) and the copolymer containing the highest HBPPMA unit. The dielectric constant for P(HBPPMA) and P(BzMA) at 1 kHz are 6.56 and 3.22, respectively. Also, those of copolymer systems were estimated between these two values. Similarly, poly(HBPPMA) and copolymers, which are prepared under the same conditions show the dissipation factor and conductivity as well.     

Depositon of ZnO on polyacrylonitrile fiber by thermal solvent coating

In this study, the surface functionalization of polyacrylonitrile (PAN) fibers was achieved by depositing ZnO nanoparticles using thermal solvent coating. surface morphology, crystalline structure, surface chemistry, thermal stability and washing stability of the ZnO coated PAN fibers were investigated by scanning electron microscope (SEM), X-ray diffractometer (XRD), Fourier transform Infra red spectroscopy (FT-IR), Thermo-gravimetric analyses (TGA) and washing stability test, respectively. In addition, the weight changes after coating and washing were studied at different coating and washing conditions. The SEM images revealed that the ZnO was well coated on the surface of the PAN fibers and the coating was obviously affected by the experimental temperature. The FT-IR spectra indicated the chemical features of the deposited ZnO nanostructures. The XRD patterns showed that there was a typical crystalline structure of ZnO nanogains formed on the PAN fibers after coating. The TGA results revealed that the thermal stability of the PAN fibers was improved by the ZnO coating. The experimental results of washing stability revealed the effect of temperature on the washing stability. Weight measurements indicated that the amount of ZnO deposited on PAN fibers increased with the increasing of coating temperature from 60 to 70 °C. Weight measurements also revealed that the weight of the ZnO coating on fibers decreased with the increase in washing temperature and washing time.     

Influences of organic-modified Fe-montmorillonite on structure, morphology and properties of polyacrylonitrile nanocomposite fibers

The Fe-montmorillonite (Fe-MMT) combined catalysis effects of Fe ion with barrier effects of silicate clays, was firstly synthesized by hydrothermal method, and then was modified by cetyltrimethyl ammonium bromide (CTAB). The organic-modified Fe-montmorillonite (Fe-OMT) was dispersed in the N, N-dimethyl formamide (DMF) and then compounded with polyacrylonitrile (PAN) solution which was dissolved in DMF. The composite solutions were electrospun to form PAN/Fe-OMT nanocomposite fibers. The influences of the Fe-OMT on the structure, morphology, thermal, flammability and mechanical properties of PAN nanocomposite fibers were respectively characterized by X-ray diffraction (XRD), High-resolution transmission electron microscopy (HRTEM), Scanning electron microscopy (SEM), Thermogravimetric analyses (TGA), Micro Combustion Calorimeter (MCC) and Electronic Single Yarn Strength Tester. It was found from XRD curves that there was not observable diffraction peak of silicate clay, indicating that the silicate clay layers were well dispersed within the PAN nanofibers. The HRTEM image indicated that the multilayer stacks of nanoclays could be found within the nanofibers and were aligned almost along the axis of the nanofibers. The SEM images showed that the diameters of nanocomposite fibers were decreased with the loading of the Fe-OMT. The TGA analyses revealed that the onset temperature of thermal degradation and charred residue at 700°C of PAN nanocomposite fibers were notably increased compared with the pure PAN nanofibers, contributing to the improved thermal stability properties. It was also observed from MCC analyses that the decreased peak of heat release rate (PHRR) of the PAN nanocomposite fibers reduced the flammability properties. The loadings of Fe-OMT increased the tensile strength of PAN nanocomposite fibers, but the elongation at break of PAN nanocomposite fibers was lower than that of the PAN nanofibers.     

Production of carbon fibers modified with ceramic powders for medical applications

Carbon fibers and precursor polyacrylonitrile (PAN) fibres that contain either silica or hydroxyapatite particles, imbedded during the spinning process, were studied in this paper. The modified PAN fibers were thermally stabilized using a multi-stage process in the temperature range between 150 to 280 °C in an oxidative environment. Subsequent carbonization leading to obtain carbon fibers was carried on at 1000 °C in an argon atmosphere. The changes of properties of composite precursor fibers taking place during stabilization and carbonization processes were investigated by the combination of Differential Scanning Calorimetry, Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy equipped with energy dispersive X-ray spectrometer and ultrasonic methods. Mechanical properties, such as tensile strength, static Young’s modulus, elongation at fracture were analyzed at each stage of thermal stabilization process. Additionally some traditional measurements like fiber diameter and mass were studied. Ceramic powders added to the spinning solution were present also in composites fibers after stabilization and carbonization process. Such modification allows to avoid the post-treatment operations, for example by coating or covering with films, which were usually necessary in order to obtain bioactive character of implants. Modification of carbon fibers using calcium phosphate or silica can lead to the development of a new materials for the manufacturing of implants which can establish direct chemical bonds with bone tissue after implantation.     

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.     

Modeling and differential evolution optimization of PAN carbon fiber production process

In this research, results of an experimental and artificial neural network fuzzy interface system (ANFIS) modeling of operating parameters on tensile strength of the carbon fibers are investigated. To do these experiments, the commercial polyacrylonitrile (PAN) fiber of Polyacryl Iran Corporation (PIC) was used as the precursors. The results show that increasing all of parameters improves tensile strength performance. ANFIS was applied to predict tensile strength of carbon fibers as a function of stabilization temperature at first stage (STFIS), stabilization temperature at second stage (STSS), stabilization temperature at third stage (STTS), stabilization temperature at fourth stage (STFOS), and carbonization temperature (CT). The optimum levels of influential factors, determined for tensile strength are STFIS 200 °C, STSS 225 °C, STTS 240 °C, STFOS 260 °C, CT, and 1400 °C. The modeling results showed that there is an excellent agreement between the experimental data and the predicted values. Furthermore, the fiber process is optimized applying differential evolution (DE) algorithm as an effective and robust optimization method.     

Preparation and characterization of poly(methylmethacrylate-coglycidyl methacrylate)/n-hexadecane nanocapsules as a fiber additive for thermal energy storage

The interest to innovative products with high added values and processes in textile field has been rapidly increasing among the other industrial fields. One of innovations in this field is to produce of innovative textiles containing phase change material (PCMs) that have thermal storage and thermo-regulation properties. This study deals with preparation and characterization of poly(methylmethacrylate-co-glycidyl methacrylate)/n-hexadecane nanocapsules containing nhexadecane as phase change material for thermal energy storage. The chemical characterization of poly(methylmethacrylateco-glycidyl methacrylate)/n-hexadecane nanocapsules was made by fourier transform infrared (FT-IR) spectroscopy method as particle size and its distribution (PSD) were studied by scanning electron microscopy (SEM). Thermal properties of nanoencapsulated n-hexadecane were determined using differential scanning calorimetry (DSC). The melting and freezing temperatures of the nanoencapsulated n-hexadecane were 17.23 and 14.85 °C respectively as the latent heats of melting and crystallization were 148.05 and −147.63 J/g respectively. Produced nanocapsules were applied to polyacrylonitrile (PAN) by means of electrospinning and surface morphology of the fibers was investigated by SEM analysis. Based on the results, it can be considered that the nanoencapsulated n-hexadecane in poly(methylmethacrylate-co-glycidyl methacrylate) have good energy storage potential to be used in fibers.     

The effect of storage environment on the infection of potato tubers byAlternaria solani

Manipulation of storage environment to provide favorable conditions for wound healing immediately after harvest reducedAlternaria solani tuber infection. Prestorage of tubers at 15.6°C for three weeks before final storage at 10°C normally maintained for commercial storage of potato chip stocks resulted in fewer and smaller lesions than constant storage at 10°C or 4.4°C or prestorage for varying periods at these temperatures. Prestorage of potatoes at a low temperature (4.4°C) for 1–3 months resulted in moreA. solani infection suggesting that low temperatures may inhibit the wound healing process more than they reduce rates ofA. solani infection or disease development. Variations in relative humidities above 75% did not have an appreciable effect on the wound healing process nor onA. solani infection.