Sandra Paszkiewicz

Influence of intercalated organoclay on the phase structure and physical properties of PTT–PTMO block copolymers

Poly(trimethylene terephthalate-block-tetramethylene oxide) (PTT–PTMO) copolymer/organoclay nanocomposites were prepared by in situ polymerization. They showed an intercalated silicate structure, as determined by X-ray diffraction and transmission electron microscopy. The influence of intercalated organoclay on the two-phase structure and mechanical properties of PTT–PTMO block copolymer was examined by using DSC and tensile tests. The DSC results imply that the silicate layers (Nanofil 32) in PTT–PTMO act as nucleation agents and accelerate the crystallization of PTT hard phase during the cooling down process from the melt. The introduction of silicate layers does not have great effect on the glass transition temperature of PTMO-rich soft phase, melting temperature of PTT hard phase, and degree of crystallinity of the nanocomposites. As the organoclay loading in the nanocomposites increase, the enhanced tensile modulus and yield stress was observed. The cyclic tensile tests showed that obtained nanocomposites have values of permanent set comparable to the neat PTT–PMO copolymer.

Detailed study on interfacial interactions in epoxy composites cured with 1-buthylimidazole containing functionalized carbon nanotubes

This work provides a detailed information on the preparation process and characterization of functionalized multiwalled carbon nanotubes/Epidian 6 nanocomposites using ARES rheometer, TGA, and DSC measurements, with the imidazole derivative as a curing agent. Scanning electron microscopy of the fracture surfaces of the composites with a total nanofiller concentration below 0.5 wt.% reveals a uniform dispersion of MWCNT with only some minor agglomerates. At the same time, the TEM analysis of the composite with a total concentration of MWCNT–COOH higher than 0.5 wt.% confirmed the presence of carbon nanotube aggregates along with a large number of places without any presence of nanoparticles in the whole volume of the epoxy matrix. Mechanical tests (bending as well as dynamic mechanical analysis) show that compared with the neat epoxy resin, the bending strength of the composite was improved by about 30 and 21% after incorporating as little as only 0.1 and 0.2 wt.% MWCNT–COOH, respectively. The work presented hereby is a continuation of a previous study on epoxy-based nanocomposites with different types of multiwalled carbon nanotubes and it is a part of a wider project on precise charting of the influence of carbon nanotubes (particularly multiwalled carbon nanotubes) in the system of epoxy resin with 1-buthylimidazole, as a curing agent.

Influence of expanded graphite (EG) and graphene oxide (GO) on physical properties of PET based nanocomposites

Abstract This work is the continuation and refinement of already published communications based on PET/EG nanocomposites prepared by in situ polymerization1, 2. In this study, nanocomposites based on poly(ethylene terephthalate) with expanded graphite were compared to those with functionalized graphite sheets (GO). The results suggest that the degree of dispersion of nanoparticles in the PET matrix has important effect on the structure and physical properties of the nanocomposites. The existence of graphene sheets nanoparticles enhances the crystallization rate of PET. It has been confirmed that in situ polymerization is the effective method for preparation nanocomposites which can avoid the agglomeration of nanoparticles in polymer matrices and improve the interfacial interaction between nanofiller and polymer matrix. The obtained results have shown also that due to the presence of functional groups on GO surface the interactions with PET matrix can be stronger than in the case of exfoliated graphene (EG) and matrix.

Phase Separation and Elastic Properties of Poly(Trimethylene Terephthalate)-block-poly(Ethylene Oxide) Copolymers

A series of poly(trimethylene terephthalate)-block-poly(ethylene oxide) (PTT-b-PEOT) copolymers with different compositions of rigid PTT and flexible PEOT segments were synthesized via condensation in the melt. The influence of the block length and the block ratio on the micro-separated phase structure and elastic properties of the synthesized multiblock copolymers was studied. The PEOT segments in these copolymers were kept constant at 1130, 2130 or 3130 g/mol, whereas the PTT content varied from 30 up to 50 wt %. The phase separation was assessed using differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA). The crystal structure of the synthesised block copolymers and their microstructure on the manometer scale was evaluated by using WAXS and SAXS analysis. Depending on the PTT/PEOT ratio, but also on the rigid and flexible segment length in PTT-b-PEO copolymers, four different domains were observed i.e.,: a crystalline PTT phase, a crystalline PEO phase (which exists for the whole series based on three types of PEOT segments), an amorphous PTT phase (only at 50 wt % content of PTT rigid segments) and an amorphous PEO phase. Moreover, the elastic deformability and reversibility of PTT-b-PEOT block copolymers were studied during a cyclic tensile test. Determined values of permanent set resultant from maximum attained stain (100% and 200%) for copolymers were used to evaluate their elastic properties.

Thermoplastic elastomers containing 2D nanofillers: montmorillonite, graphene nanoplatelets and oxidized graphene platelets

Abstract This paper presents a comparative study on which type of platelets nanofiller, organic or inorganic, will affect the properties of thermoplastic elastomer matrix in the stronger manner. Therefore, poly(trimethylene terephthalate-block-poly(tetramethylene oxide) copolymer (PTT-PTMO) based nanocomposites with 0.5 wt.% of clay (MMT), graphene nanoplatelets (GNP) and graphene oxide (GO) have been prepared by in situ polymerization. The structure of the nanocomposites was characterized by transmission electron microscopy (TEM) in order to present good dispersion without large aggregates. It was indicated that PTT-PTMO/GNP composite shows the highest crystallization temperature. Unlike the addition of GNP and GO, the introduction of MMT does not have great effect on the glass transition temperature of PTMO-rich soft phase. An addition of all three types of nanoplatelets in the nanocomposites caused the enhancement in tensile modulus and yield stress. Additionally, the cyclic tensile tests showed that prepared nanocomposites have values of permanent set slightly higher than neat PTT-PTMO.

Nanocomposites based on polymer blends: enhanced interfacial interactions in polycarbonate/ethylene-propylene copolymer blends with multi-walled carbon nanotubes

Abstract In this article, the phase separation in the melt blended polycarbonate (PC) and ethylene propylene copolymer (EPC) has been studied with dynamic mechanical thermal analysis (DMTA) and scanning electron microscopy (SEM). Two glass transition temperatures on the tan δ curves were detected. This confirms the immiscibility of PC and EPC phases. Different content of multi-walled carbon nanotubes (MWCNTs) were added to the PC/EPC blends and the interfacial adhesion between MWCNTs and PC/EPC blend were shown using transmission electron microscopy (TEM). The MWCNTs were located in the PC phase and at the interfaces of PC and EPC phases. Moreover, the storage modulus (E′) of polymer blends was changed by the increasing content of EPC elastomer and MWCNTs. The value of E′ of PC decreased with an incorporation of EPC. While, along with an addition of MWCNTs in the PC/EPC blends an increase of E′ was visible. The strong interfacial interactions between the matrix and MWCNTs played the main role in increasing the values of the E′ of the nanocomposites.

Oxygen barrier properties and melt crystallization behavior of poly(ethylene terephthalate)/graphene oxide nanocomposites

Poly(ethylene terephthalate) nanocomposites with low loading (0.1-0.5 wt%) of graphene oxide (GO) have been prepared by using in situ polymerization method. TEM study of nanocomposites morphology has shown uniform distribution of highly exfoliated graphene oxide nanoplatelets in PET matrix. Investigations of oxygen permeability of amorphous films of nanocomposites showed that the nanocomposites had better oxygen barrier properties than the neat PET. The improvement of oxygen permeability for PET nanocomposite films over the neat PET is approximately factors of 2-3.3. DSC study on the nonisothermal crystallization behaviors proves that GO acts as a nucleating agent to accelerate the crystallization of PET matrix. The evolution of the lamellar nanostructure of nanocomposite and neat PET was monitored by SAXS during nonisothermal crystallization from the melt. It was found that unfilled PET and nanocomposite with the highest concentration of GO (0.5 wt%) showed almost similar values of the long period (L = 11.4 nm for neat PET and L = 11.5 nm for PET/0.5GO).

Electrically and Thermally Conductive Low Density Polyethylene-Based Nanocomposites Reinforced by MWCNT or Hybrid MWCNT/Graphene Nanoplatelets with Improved Thermo-Oxidative Stability

In this paper, the electrical and thermal conductivity and morphological behavior of low density polyethylene (LDPE)/multi-walled carbon nanotubes (MWCNTs) + graphene nanoplatelets (GNPs) hybrid nanocomposites (HNCs) have been studied. The distribution of MWCNTs and the hybrid of MWCNTs/GNPs within the polymer matrix has been investigated with scanning electron microscopy (SEM). The results showed that the thermal and electrical conductivity of the LDPE-based nanocomposites increased along with the increasing content of carbon nanofillers. However, one could observe greater improvement in the thermal and electrical conductivity when only MWCNTs have been incorporated. Moreover, the improvement in tensile properties and thermal stability has been observed when carbon nanofillers have been mixed with LDPE. At the same time, the increasing content of MWCNTs and MWCNTs/GNPs caused an increase in the melt viscosity with only little effect on phase transition temperatures.

Interfacial interactions in PTT–PTMO/polyhedral oligomeric silsesquioxane (POSS) nanocomposites and their impact on mechanical, thermal, and dielectric properties

Poly(trimethylene terephthalate–block–tetramethylene oxide) (PTT–PTMO)/polyhedral oligomeric silsesquioxane (POSS) nanocomposites, synthesized by in situ polymerization, are characterized in detail in terms of interfacial interactions between functional groups on the surface of POSS and polymer chains. The impact of POSS incorporation on the molecular mobility is investigated by means of dielectric spectroscopy. It is found that PTT–PTMO/POSS nanocomposites exhibit higher values of stress at strain of 100% that in comparison with neat PTT–PTMO might result from the influence of POSS particles on the molecular mobility of polymer chains, which is probably due to the interfacial interactions between functional groups on the surface of POSS particles with the polymer matrix. Moreover, it is found that there is no variation of the segmental relaxation for the nanocomposite investigated and there is an increase in the interfacial polarization induced by the presence of POSS as seen in the increment of the real part of the dielectric permittivity.

Modification of substandard EPDM with amorphous thermoplastic polyesters (PETG and PEF): microstructure and physical properties

Abstract The phase morphology, thermal behavior and mechanical properties of two series of polymer blends based on ethylene/propylene/diene rubber (EPDM) and amorphous homologues of poly(ethylene terephthalate), i.e. glycol modified poly(ethylene terephthalate) (PETG) and poly(ethylene furanoate) (PEF), were investigated. The morphology of the blends shows a two phase structure in which the minor phase (amorphous polyester) is dispersed as domains in the major (EPDM) continuous matrix phase. Differential calorimetry studies confirmed that both systems were immiscible and exhibits two glass transitions. The melting peak area of EPDM in the blends decreased as the amount of the other component increased. The values of stress at strain of 100% were improved upon the increasing content of PETG in EPDM system, while only slight decrease of this value was observed. Moreover, the strong improvement of hardness and thermo-oxidative stability along with an increasing content of amorphous polyester phase was reported.