‘Unfolding the self through time’: travels of memory and twists of identity in the works of Irena F. Karafilly, Lisa Appignanesi and Anne Michaels

2008-2009Il lavoro approfondisce, attraverso le opere di F. Karafilly, Lisa Appianesi ed Anne Michaels, il rapporto tra nmemoria e identità, sia sul piano umano sia su quello artistico. Il primo capitolo si incentra sull'analisi dell'interrelazione tra storia, memoria e identità nell'opera 'Ashes and Miracles' della scrittrice Irena Friedman Katafilly. Vengono quindi discusse le ambiguità della memoria nel processo di decostruzione e di ricostruzione dell'identità dell'immigrato e anlizzato l'approccio e le considerazioni dell'autrice sul pregiudizio, la tolleranza e la riconciliazione nella società multietnica. Nel secondo capitolo l'analisi si focalizza sull'opera 'The Stranger in a Plumed Hat' esull'analisi dell'impatto della malattia cerebrale di Alzheimer, che aveva colpito la madre della scrittrice sulla memoria e la relativa percezione. Il terzo capitolo riprende l'analisi del rapporto tra memoria e identità sulla scia della guerra, attraverso l'esame dell'opera 'Losing the Dead' di Lisa Appignanesi, scrittrice canadese di origine polacco-ebrea. si esamina, quindi, il gioco delle identità coinvolte nella sopravvivenza della propria famiglia alle atrocità della guerra. La quarta parte del lavoro esamina le opere dell'Appignanesi che riflettoo sul legame tra l'identità, la memoria, la psicoanalisi e l'arte, considerando i vari approcci critici al mito femminile. L'ultimo capitolo analizza il romanzo 'Fugitive Pieces' dei Anne Michaels, in cui viene raccontata la tragedia della Shoa.VIII n.s

Bio-Based Polyurethane Networks Derived from Liquefied Sawdust

The utilization of forestry waste resources in the production of polyurethane resins is a promising green alternative to the use of unsustainable resources. Liquefaction of wood-based biomass gives polyols with properties depending on the reagents used. In this article, the liquefaction of forestry wastes, including sawdust, in solvents such as glycerol and polyethylene glycol was investigated. The liquefaction process was carried out at temperatures of 120, 150, and 170 °C. The resulting bio-polyols were analyzed for process efficiency, hydroxyl number, water content, viscosity, and structural features using the Fourier transform infrared spectroscopy (FTIR). The optimum liquefaction temperature was 150 °C and the time of 6 h. Comprehensive analysis of polyol properties shows high biomass conversion and hydroxyl number in the range of 238–815 mg KOH/g. This may indicate that bio-polyols may be used as a potential substitute for petrochemical polyols. During polyurethane synthesis, materials with more than 80 wt% of bio-polyol were obtained. The materials were obtained by a one-step method by hot-pressing for 15 min at 100 °C and a pressure of 5 MPa with an NCO:OH ratio of 1:1 and 1.2:1. Dynamical-mechanical analysis (DMA) showed a high modulus of elasticity in the range of 62–839 MPa which depends on the reaction conditions.The authors would like to thank the National Science Centre of Poland (No. 2018/02/X/ST5/02784) for financial support

Predicted Studies of Branched and Cross-Linked Polyurethanes Based on Polyhydroxybutyrate with Polycaprolactone Triol in Soft Segments

The number of cross-links in the non-linear polyurethane structure is the basic factor affecting its properties. Selected properties of aliphatic polyurethanes with soft segments made of different amounts of polycaprolactonetriol, polycaprolactonediol and synthetic, telechelic poly([R,S]-3-hydroxybutyrate) were determined. On the basis of changes in polyurethane properties, the correlation between these properties and the construction of soft segments was found. The structure of polyurethanes, their morphology, hydrophilicity, thermal and mechanical properties were examined. These properties were changed linearly up to 15% content of polycaprolactonetriol in soft segments. A further increase in the amount of triol causes that these properties are mainly determined by the high number of cross-links.This research was founded by the National Science Center Miniatura 2 project no. 2018/02/X/ST5/02005 and partially by the UMG research project no. WPiT/2020/PZ/01

Highly hydrophobic cellulose acetate mats modified with poly(ethylene oxide-b-propylene oxide-b-ethylene oxide) triblock copolymer and TiO2 nanoparticles by electrospinning

Cellulose acetate (CA) mats modified with poly(ethylene oxide-b-propylene oxide-b-ethylene oxide) (PEO-b-PPO-b-PEO or EPE) and sol–gel synthesised titanium oxide (TiO2) nanoparticles were successfully fabricated by using electrospinning technique. Under the same preparation conditions, higher spinnability was achieved for EPE triblock copolymers modified mats. All fabricated mats showed a micrometric multilayer structure, which enabled layer-by-layer peeling. The addition of TiO2 nanoparticles facilitated the peeling process. The diameter of the fibres was ~ 3 times lower after the incorporation of sol–gel synthesised TiO2 nanoparticles. TEM images confirmed that under electrospinning conditions the PPO block domains were able to microphase separated from the PEO block/CA phase. Additionally, the introduction of sol–gel synthesised TiO2 nanoparticles led to an inorganic network formation with nanoparticle size equal to ~ 8 nm in diameter. Moreover, the addition of TiO2 nanoparticles increased the hydrophobicity of the mats and their self-cleaning ability, being more effective for TiO2/CA than for TiO2-EPE/CA due to the partial absorption of water by EPE triblock copolymer. Young’s modulus of fabricated mats improved drastically with the addition of TiO2 nanoparticles, as well as their physical integrity in polar and nonpolar solvents. Fabricated mats with enhanced spinnability, which maintain CA mat features as well as the properties associated with sol–gel synthesised TiO2 nanoparticles, can find a wide range of applications.Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. This work was founded by Spanish Ministry of Science, Innovation and Universities and European Union (MICINN/FEDER and UE) in the frame of PGC2018-097699-B-I00 and PID2021-126417NB-I00 projects, and by Basque Government in frame of PIBA19-0044. J.G.-H.-de-M. thanks Basque Government for PhD Fellowship (PRE_2021_2_0044)

Degradability of Polyurethanes and Their Blends with Polylactide, Chitosan and Starch

One of the methods of making traditional polymers more environmentally friendly is to modify them with natural materials or their biodegradable, synthetic equivalents. It was assumed that blends with polylactide (PLA), polysaccharides: chitosan (Ch) and starch (St) of branched polyurethane (PUR) based on synthetic poly([R,S]-3-hydroxybutyrate) (R,S-PHB) would degrade faster in the processes of hydrolysis and oxidation than pure PUR. For the sake of simplicity in the publication, all three modifiers: commercial PLA, Ch created by chemical modification of chitin and St are called bioadditives. The samples were incubated in a hydrolytic and oxidizing environment for 36 weeks and 11 weeks, respectively. The degradation process was assessed by observation of the chemical structure as well as the change in the mass of the samples, their molecular weight, surface morphology and thermal properties. It was found that the PUR samples with the highest amount of R,S-PHB and the lowest amount of polycaprolactone triol (PCLtriol) were degraded the most. Moreover, blending with St had the greatest impact on the susceptibility to degradation of PUR. However, the rate of weight loss of the samples was low, and after 36 weeks of incubation in the hydrolytic solution, it did not exceed 7% by weight. The weight loss of Ch and PLA blends was even smaller. However, a significant reduction in molecular weight, changes in morphology and changes in thermal properties indicated that the degradation of the samples should occur quickly after this time. Therefore, when using these polyurethanes and their blends, it should be taken into account that they should decompose slowly in their initial life. In summary, this process can be modified by changing the amount of R,S-PHB, the degree of cross-linking, and the type and amount of second blend component added (bioadditives).This research was founded by the National Science Center Poland Miniatura 2 project no. 2018/02/X/ST5/02005 and partially by the UMG research project no. WZNJ/2021/PZ/02

Modified ‘one amino acid-one codon’ engineering of high GC content TaqII-coding gene from thermophilic Thermus aquaticus results in radical expression increase

BACKGROUND: An industrial approach to protein production demands maximization of cloned gene expression, balanced with the recombinant host’s viability. Expression of toxic genes from thermophiles poses particular difficulties due to high GC content, mRNA secondary structures, rare codon usage and impairing the host’s coding plasmid replication. TaqII belongs to a family of bifunctional enzymes, which are a fusion of the restriction endonuclease (REase) and methyltransferase (MTase) activities in a single polypeptide. The family contains thermostable REases with distinct specificities: TspGWI, TaqII, Tth111II/TthHB27I, TspDTI and TsoI and a few enzymes found in mesophiles. While not being isoschizomers, the enzymes exhibit amino acid (aa) sequence homologies, having molecular sizes of ~120 kDa share common modular architecture, resemble Type-I enzymes, cleave DNA 11/9 nt from the recognition sites, their activity is affected by S-adenosylmethionine (SAM). RESULTS: We describe the taqIIRM gene design, cloning and expression of the prototype TaqII. The enzyme amount in natural hosts is extremely low. To improve expression of the taqIIRM gene in Escherichia coli (E. coli), we designed and cloned a fully synthetic, low GC content, low mRNA secondary structure taqIIRM, codon-optimized gene under a bacteriophage lambda (λ) P( R ) promoter. Codon usage based on a modified ‘one amino acid–one codon’ strategy, weighted towards low GC content codons, resulted in approximately 10-fold higher expression of the synthetic gene. 718 codons of total 1105 were changed, comprising 65% of the taqIIRM gene. The reason for we choose a less effective strategy rather than a resulting in high expression yields ‘codon randomization’ strategy, was intentional, sub-optimal TaqII in vivo production, in order to decrease the high ‘toxicity’ of the REase-MTase protein. CONCLUSIONS: Recombinant wt and synthetic taqIIRM gene were cloned and expressed in E. coli. The modified ‘one amino acid–one codon’ method tuned for thermophile-coded genes was applied to obtain overexpression of the ‘toxic’ taqIIRM gene. The method appears suited for industrial production of thermostable ‘toxic’ enzymes in E. coli. This novel variant of the method biased toward increasing a gene’s AT content may provide economic benefits for industrial applications

Compatibility of Sustainable Mater-Bi/poly(ε-caprolactone)/cellulose Biocomposites as a Function of Filler Modification

Despite their popularity and multiplicity of applications, wood–polymer composites (WPCs) still have to overcome particular issues related to their processing and properties. The main aspect is the compatibility with plant-based materials which affects the overall performance of the material. It can be enhanced by strengthening the interfacial adhesion resulting from physical and/or chemical interactions between the matrix and filler, which requires introducing a compatibilizer or a proper modification of one or both phases. Herein, the impact of cellulose filler modifications with varying contents (1–10 wt%) of hexamethylene diisocyanate (HDI) on the compatibility of Mater-Bi/poly(ε-caprolactone) (PCL)-based biocomposites was evaluated. An analysis of surface wettability revealed that the filler modification reduced the hydrophilicity gap between phases, suggesting compatibility enhancement. It was later confirmed via microscopic observation (scanning electron microscopy (SEM) and atomic force microscopy (AFM)), which pointed to the finer dispersion of modified particles and enhanced quality of the interface. The rheological analysis confirmed increased system homogeneity by the reduction in complex viscosity. In contrast, thermogravimetric analysis (TGA) indicated the efficient modification of filler and the presence of the chemical interactions at the interface by the shift of thermal decomposition onset and the changes in the degradation course.This work was supported by the National Science Centre (NCN, Poland) in the frame of SONATINA 2 project 2018/28/C/ST8/00187—Structure and properties of lignocellulosic fillers modified in situ during reactive extrusion. The study was partially co-funded under project with grants for education allocated by the Ministry of Science and Higher Education in Poland executed under the subject of No 0613/SBAD/4820

The Redox Imbalance and the Reduction of Contractile Protein Content in Rat Hearts Administered with L-Thyroxine and Doxorubicin

Oxidative stress and disorders in calcium balance play a crucial role in the doxorubicin-induced cardiotoxicity. Moreover, many cardiotoxic targets of doxorubicin are regulated by iodothyronine hormones. The aim of the study was to evaluate effects of tetraiodothyronine (0.2, 2 mg/L) on oxidative stress in the cardiac muscle as well as contractility and cardiomyocyte damage markers in rats receiving doxorubicin (1.5 mg/kg) once a week for ten weeks. Doxorubicin was administered alone (DOX) or together with a lower (0.2T4 + DOX) and higher dose of tetraiodothyronine (2T4 + DOX). Two groups received only tetraiodothyronine (0.2T4, 2T4). Coadministration of tetraiodothyronine and doxorubicin increased the level of lipid peroxidation products and reduced RyR2 level when compared to untreated control and group exposed exclusively to doxorubicin. Insignificant differences in SERCA2 and occasional histological changes were observed. In conclusion, an increase of tetraiodothyronine level may be an additional risk factor of redox imbalance and RyR2 reduction in anthracycline cardiotoxicity

Isothermal Crystallization Kinetics and Morphology of Double Crystalline PCL/PBS Blends Mixed with a Polycarbonate/MWCNTs Masterbatch

In this work, the 70/30 and 30/70 w/w polycaprolactone (PCL)/polybutylene succinate (PBS) blends and their corresponding PCL/PBS/(polycarbonate (PC)/multiwalled carbon nanotubes (MWCNTs) masterbatch) nanocomposites were prepared in a twin-screw extruder. The nanocomposites contained 1.0 and 4.0 wt% MWCNTs. The blends showed a sea-island morphology typical of immiscible blends. For the nanocomposites, three phases were formed: (i) The matrix (either PCL- or PBS-rich phase depending on the composition), (ii) dispersed polymer droplets of small size (either PCL- or PBS-rich phase depending on the composition), and (iii) dispersed aggregates of tens of micron sizes identified as PC/MWCNTs masterbatch. Atomic force microscopy (AFM) results showed that although most MWCNTs were located in the PC dispersed phase, some of them migrated to the polymer matrix. This is due to the partial miscibility and intimate contact at the interfaces between blend components. Non-isothermal differential scanning calorimetry (DSC) scans for the PCL/PBS blends showed an increase in the crystallization temperature (Tc) of the PCL-rich phase indicating a nucleation effect caused by the PBS-rich phase. For the nanocomposites, there was a decrease in Tc values. This was attributed to a competition between two effects: (1) The partial miscibility of the PC-rich and the PCL-rich and PBS-rich phases, and (2) the nucleation effect of the MWCNTs. The decrease in Tc values indicated that miscibility was the dominating effect. Isothermal crystallization results showed that the nanocomposites crystallized slower than the neat blends and the homopolymers. The introduction of the masterbatch generally increased the thermal conductivity of the blend nanocomposites and affected the mechanical properties.Thandi P. Gumede was financially supported by the National Research Foundation and the Sasol Inzalo Foundation in South Africa, while the POLYMAT/UPV/EHU team was funded by the following projects: “UPV/EHU Infrastructure: INF 14/38”; “Mineco/FEDER: SINF 130I001726XV1/Ref: UNPV13–4E–1726” and MINECO MAT2017-83014-C2-1-P. The publication of this article was funded by the Qatar National Library