Michał Puchalski

Chemically Driven Printed Textile Sensors Based on Graphene and Carbon Nanotubes

The unique properties of graphene, such as the high elasticity, mechanical strength, thermal conductivity, very high electrical conductivity and transparency, make them it an interesting material for stretchable electronic applications. In the work presented herein, the authors used graphene and carbon nanotubes to introduce chemical sensing properties into textile materials by means of a screen printing method. Carbon nanotubes and graphene pellets were dispersed in water and used as a printing paste in the screen printing process. Three printing paste compositions were prepared—0%, 1% and 3% graphene pellet content with a constant 3% carbon nanotube mass content. Commercially available materials were used in this process. As a substrate, a twill woven cotton fabric was utilized. It has been found that the addition of graphene to printing paste that contains carbon nanotubes significantly enhances the electrical conductivity and sensing properties of the final product.

Influence of the calender temperature on the crystallization behaviors of polylactide spun-bonded non-woven fabrics:

In this paper the influence of calender temperature on the crystallization behavior of polylactide (PLA) non-woven fabrics during their manufacturing by the spun-bonding technique is described. Non-woven samples were studied by wide-angle X-ray diffraction, differential scanning calorimetry and birefringence. In addition, physical–mechanical properties of the non-woven fabrics were determined. The results are discussed in terms of structural changes of PLA and meso-phase content during the calendering process in the temperature range 70–130℃. The rebuilding of the supermolecular structure of the investigated samples of PLA fabrics under the influence of increasing calender temperature is observed in terms of the disorder-to-order phase transition (ά to α form) during heating around 110℃, and increased degree of crystallinity up to 100℃. The presented structural rebuild of PLA explains observed changes of physical–mechanical properties of the non-woven fabrics obtained at different calendering temperatures. During calendering above 100℃, thermal degradation of PLA occurs at the point of contact between the non-woven fabrics and the calender rollers.

Application of melt-blown technology in the manufacturing of a solvent vapor-sensitive, non-woven fabric composed of poly(lactic acid) loaded with multi-walled carbon nanotubes

We evaluated a solvent vapor-sensitive, non-woven fabric made from a biodegradable, poly(lactic acid) (PLA) polymer loaded with multi-walled carbon nanotubes. The sensory properties of the fabric were obtained by optimizing the process parameters for manufacturing the melt-blown, non-woven fabric composed of 98% PLA 4060D (Nature Works) and 2% multi-walled carbon nanotubes (Nanocyl®). The diffusion of polar and non-polar solvent molecules influenced the electron flow between the separated carbon nanotubes in percolation paths built into the PLA, resulting in an increase of the resistance of the melt-blown, non-woven fabrics. The statistically significant differences between the mean values of electrical resistance before and after the influence of the tested solvent vapors were achieved for the non-woven fabrics manufactured at high air velocity and low extruder screw speed, taking the values of 30 m3/h and 20 rpm, respectively. The results obtained for the non-woven fabric manufactured in the optimal conditions show that methanol vapor response has the lowest amplitude of 15%, whereas for benzene, acetone and toluene sensitivity reaches values of 60%, 40%, and 35%, respectively. The values of the relative resistance amplitude correspond with Flory–Huggins interaction parameters κPLA\benzene < κPLA\acetone < κPLA\toluene < κPLA\methanol.

Effect of processing variables on the thermal and physical properties of poly(L-lactide) spun bond fabrics

In this paper, the influence of the take-up velocity (Vt–u) of fibers on the molecular ordering and ά – α form transition of polylactide (PLA) non-woven fabrics during their manufacturing by spun-bonding is described. Non-woven samples were studied by wide-angle X-ray diffraction, differential scanning calorimetry and Fourier transform infrared spectroscopy. In addition, the physical and mechanical properties of the non-woven fabrics were determined. The results are discussed in terms of the structural changes of the PLA and the meso-phase content during the spun-bonded non-woven fabric forming process. This technological process includes preliminary molecular ordering of the PLA fibers in a downstream spinning block and crystallization on a calender system at a temperature higher than the glass transition. The molecular ordering of the investigated PLA fabric samples under different technological conditions was observed as follows: creation of the meso-phase and a disorder-to-order phase transition (ά to α form) during heating to approximately 110℃ and an increase in the degree of crystallinity for take-up velocities higher than 1400 m/min. The structural changes of the PLA explain the observed changes in the physical and mechanical properties of the non-woven fabrics obtained under different technological conditions.

Investigation of the Influence of PLA Molecular Structure on the Crystalline Forms (α’ and α) and Mechanical Properties of Wet Spinning Fibres

In this paper, the influence of the molecular structure of polylactide (PLA)—characterised by its molar mass and content of d-lactide isomer—on the molecular ordering and α’–α form transition during fibre manufacturing by the wet spinning method is described. Fibres were studied by wide-angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC). Additionally, the physical and mechanical properties of the fibres were determined. This study also examines the preliminary molecular ordering and crystallisation of PLA fibres at various draw ratios. The performed experiments clearly show the dependence of the molecular ordering of PLA on the molar mass and d-lactide content during the wet spinning process. The fibres manufactured from PLA with the lowest content of d-lactide and the lowest molar mass were characterised by a higher tendency for crystallisation and a higher possibility to undergo the disorder-to-order phase transition (α’ to α form). The structural changes in PLA explain the observed changes in the physical and mechanical properties of the obtained fibres.

Antibacterial properties of polypropylene textiles modified by poly(2-(N,N-dimethyloamino ethyl) methacrylate)

Polypropylene nonwoven fabrics samples were modified using poly(2-(N,N-dimethyloamino ethyl) methacrylate) (PDAMA) and silver-containing layers. The structure of the material after modification was confirmed using scanning electron mocroscope, energy-dispersive X-ray spectroscopy, Fourier Transfer Infrared Spectroscopy (FTIR), and electro-kinetic measurements. It was found that samples with external PDAMA layers have excellent activity against Staphylococcus aureus under dynamic contact conditions. In contrast, samples finished with deposited silver showed little antimicrobial effect. Antibacterial tests conducted under static conditions showed no antibacterial activity irrespective of the deposited layers.

N,N,N-trimethyl chitosan as an efficient antibacterial agent for polypropylene and polylactide nonwovens

Abstract The paper presents a method of depositing N,N,N-trimethyl chitosan (TMC) layers onto polypropylene and polylactide nonwovens. A two-step modification procedure is applied: first, grafting the nonwovens with acrylic acid and next layer-by-layer deposition. Turbidimetric measurements confirm the creation of polycomplexes between grafted poly(acrylic acid) and deposited TMC. The created material structure is evaluated using gravimetric analysis, reflectance Fourier transform infrared spectroscopy, scanning electron microscopy, energy dispersive spectroscopy measurements and pH-metric titration. The modified material exhibits good antibacterial properties against Gram-positive bacteria Staphylococcus aureus.

Ozone treatment of jute fibers

Oxidation of cellulosic materials is required in many fields such as textile processing, natural fiber composites, medical utilization, and so on. The present study was designed to explore the possibility of ozone treatment as a greener oxidation process for jute fibers. Ozone gas was used for the treatment of waste jute fibers for different time periods in a humid atmosphere. Several characterization techniques, namely physical appearance, fiber mechanical properties, the copper number, Fourier transform infrared spectroscopy, wide-angle X-ray diffraction, scanning electron microscopy, moisture regain percentage and lightness values (L), were used to assess the effect of treatment on jute fibers. Results showed that fiber tensile properties weaken gradually as a function of treatment time, and surface functional groups alter accordingly. Changes in crystallinity after ozone treatment were also observed. Physically the fiber bundles were split into brittle single fibers, and the L value increased from a brownish shade to lighter color.

Antimicrobial properties of silver nanoparticles against biofilm formation by Pseudomonas aeruginosa on archaeological textiles

The aims of this work were to: (i) microscopically analyse the pre- and post-Columbian archaeological textiles using Scanning Electron Microscopy with Energy Dispersive X-Ray Analysis (SEM-EDX); (ii) microbiologically analyse the archaeological textiles (from the Southern Andean Area, La Plata Museum); (iii) determine the ability of Pseudomonas sp. isolates from archaeological textiles to biofilm formation by SEM; (iv) assess the anti-biofilm properties of AgNPs protecting cotton against Pseudomonas sp. Results showed the presence of bacteria with proteolytic and lipolytic activities on archaeological textiles, including Clostridium sp. and Pseudomonas aeruginosa. Two nucleotide sequences of 16S ribosomal RNA gene of P. aeruginosa strains were deposited in GeneBank NCBI database with accession numbers: KP842564 (strain 1) and KP842565 (strain 2). Those strains exhibited different morphological and growth characteristics: strain 1 with ability to form biofilms on archaeological textiles was rod-shaped, produced bluish-green pigment, and smaller than strain 2; and strain 2 was pleomorphic and produced brown pigment. The use of silver nanoparticles (90 ppm, φ 10–80 nm) allowed to protecting textiles against P. aeruginosa growth by 63%–97%, depending on the strain and exposition time.

Molecular and Supramolecular Changes in Polybutylene Succinate (PBS) and Polybutylene Succinate Adipate (PBSA) Copolymer during Degradation in Various Environmental Conditions

In this paper, the influence of the various degradation conditions, on the molecular and supramolecular structure of polybutylene succinate (PBS) and polybutylene succinate adipate (PBSA) copolymer during degradation is described. The experiment was carried out by the use of injection molded samples and normalized conditions of biodegradation in soil, composting and artificial weathering. Materials were studied by size-exclusion chromatography (SEC) coupled with multiangle laser light scattering (MALLS) detection and wide-angle X-ray diffraction (WAXD). Additionally, the physical and mechanical properties of the samples were determined. The performed experiments clearly show difference impacts of the selected degradation conditions on the macroscopic, supramolecular and molecular parameters of the studied aliphatic polyesters. The structural changes in PBS and PBSA explain the observed changes in the physical and mechanical properties of the obtained injection molded samples.