14 research outputs found
Modelling The Volatility of Frankfurt Stock Exchange (DAX) Returns Using hybrid Models
Recently, the interest of researchers in the use of hybrid models in the process of analyzing model time series with fluctuations and forecasting fluctuations in financial time series has increased significantly. Hybrid ARMA-GARCH models were created for medium- and long-term forecasts of time series of financial market index prices: ARMA models are used to analyze their linear component, which is a combination of autoregressive models and moving average models, and GARCH models are used to analyze the nonlinear component. which are generalized autoregressive models that depend on the nonconstancy of variance models. Hybrid ARMA-GARCH models eliminate the weaknesses and gaps that exist in each group of models (ARMA and GARCH) separately, which increases their forecasting accuracy and reliability, so they have already been successfully applied to model and forecast daily stock returns for three standard indices in the USA. The purpose of this article is to investigate which of the hybrid ARMA-GARCH models is optimal for forecasting the return of the DAX index, which is the most important stock index of the German securities market. It is the German equivalent of the American Dow Jones Index, has been calculated since 1988 by Deutsche Börse AG and reflects the total return on capital of the largest stock companies listed on the Frankfurt Stock Exchange (currently 40; by 2021 â 30): calculated as a weighted average of capitalization of the value of Free Float share prices on the Xetra electronic exchange, and also takes into account dividends on shares, assuming that the dividend is reinvested in the share on which it was accrued. The database of this study consisted of the daily closing prices of the DAX index presented on the official website of the Frankfurt Stock Exchange during the period from 01.01.2018 to 09.30.2023 (altogether about 1,500 observations), the stability of the time series was assessed using Expanded Dickey Fuller Liquidity (ADF). The article proposes 7 hybrid models, from which the one that is best suited for modeling the volatility of the DAX index is selected. It is an ARMA (2,3)-EGARCH (1,1) model because it captures volatility and leverage effects on DAX returns and its expected returns more than other models. The selection of the best alternative from the developed array of hybrid models was carried out according to the following criteria: AIC (Akaike Information Criterion), BIC (Bayesian Information Criterion), H-QIC (Hannan-Quinn Information Criterion)
Analyse numérique et expérimentale du comportement des éléments de structures en bois renforcés par des tissus composites(CFRP)
Le renforcement des structures en bĂątiment, par des matĂ©riaux composites Ă base de fibre de carbone CFRP, est une technique connue de rĂ©habilitation. Dans le cadre de cette Ă©tude nous analyserons des structures bois, et plus prĂ©cisĂ©ment le confinement des poteaux par un polymĂšre renforcĂ© de fibres de carbone. La prĂ©sentation dâune approche numĂ©rique de modĂ©lisation du comportement des cylindres en bois enveloppĂ©s et confinĂ©s par un tissu CFRP reprĂ©sente lâobjectif principal de ce travail. Une mĂ©thodologie numĂ©rique de prĂ©diction du comportement mĂ©canique de ce composite est mise en place, En particulier, on sâintĂ©resse Ă lâĂ©tude du comportement plastique anisotrope du matĂ©riau bois avec effet du renforcement. Les aspects thĂ©oriques et numĂ©riques du modĂšle proposĂ© sont dĂ©taillĂ©s. LâintĂ©gration numĂ©rique des Ă©quations constitutives du modĂšle utilisant un schĂ©ma implicite itĂ©ratif basĂ© sur la technique des corrections radiale est discutĂ©e. La rĂ©solution du problĂšme dâĂ©quilibre global est assurĂ©e par un schĂ©ma Dynamique Explicite. Lâapplication est ensuite faite Ă la simulation des Ă©prouvettes circulaires en bois renforcĂ©es par CFRP. Des comparaisons avec les rĂ©sultats expĂ©rimentaux sont rĂ©alisĂ©es et discutĂ©es
Modélisation du comportement non-linéaire des poteaux en bois renforcés par la fibre de carbone
Lâobjectif principal de cet article est la mise au point dâune mĂ©thodologie numĂ©rique de
prĂ©vision du comportement local dâun procĂ©dĂ© de renforcement des poteaux en bois par la
fibre de carbone. En particulier, on sâintĂ©resse Ă lâĂ©tude du comportement
élasto-plastique du matériau bois avec effet du renforcement. Une modélisation basée sur
la thermodynamique des processus irrĂ©versibles avec variables dâĂ©tat est utilisĂ©e pour
traduire le couplage entre le comportement plastique Ă Ă©crouissage isotrope et lâeffet du
renforcement. Les aspects théoriques et numériques de cette formulation sont décrits en
dĂ©tail. La rĂ©solution du problĂšme dâĂ©quilibre global est assurĂ©e par un schĂ©ma Dynamique
Explicite. La validation de la procédure de calcul implémentée dans ABAQUS/Explicit est
faite sur la simulation dâun essai de compression des Ă©prouvettes circulaires en bois
renforcées par la fibre de carbone. Les résultats des simulations sont confrontés à ceux
de lâexpĂ©rience
Fast IR-Actuated Shape-Memory Polymers Using in Situ Silver Nanoparticle-Grafted Cellulose Nanocrystals
In recent years, shape-memory polymers (SMPs) have gained a key position in the realm of actuating applications from daily life products to biomedical and aeronautic devices. Most of these SMPs rely mainly on shape changes upon direct heat exposure or after stimulus conversion (e.g. magnetic field and light) to heat, but this concept remains significantly limited when both remote control and fine actuation are demanded. In the present study, we propose to design plasmonic silver nanoparticles (AgNPs) grafted onto cellulose nanocrystals (CNCs) as an efficient plasmonic system for fast and remote actuation. Such CNC-g-AgNPs "nanorod-like" structures thereby allowed for a long-distance and strong coupling plasmonic effect between the AgNPs along the CNC axis, thus ensuring a fast photothermal shape-recovery effect upon IR light illumination. To demonstrate the fast and remote actuation promoted by these structures, we incorporated them at low loading (1 wt %) into poly(Ï”-caprolactone) (PCL)-based networks with shape-memory properties. These polymer matrix networks were practically designed from biocompatible PCL oligomers end-functionalized with maleimide and furan moieties in the melt on the basis of thermoreversible Diels-Alder reactions. The as-produced materials could find application in the realm of soft robotics for remote object transportation or as smart biomaterials such as self-tightening knots with antibacterial properties related to the presence of the AgNPs.SCOPUS: ar.jinfo:eu-repo/semantics/publishe
A multilayer coating with optimized properties for corrosion protection of Al
International audienceA barrier multilayer coating comprising of a plasma polymer film, a grafted layer and a mechanically reinforced acrylic layer is reported in this work
Preparation of Cellulose Nanocrystal-Reinforced Poly(lactic acid) Nanocomposites through Noncovalent Modification with PLLA-Based Surfactants
Cellulose
nanocrystal (CNC)-reinforced polyÂ(lactic acid) (PLA)
nanocomposites were prepared by twin-screw extrusion followed by injection-molding
using a masterbatch approach. Noncovalent modification of CNCs was
performed with two different polyÂ(l-lactide) (PLLA)-based surfactants to improve the
filler/matrix compatibility. They both have a PLLA block that is expected
to improve the compatibility with the PLA matrix and differ by the
polar head. It consists of either a polyÂ(ethylene glycol) (PEG) block
(PEG-<i>b</i>-PLLA) or an imidazolium group (Im-PLLA), that
is able to interact with the surface of
the CNCs. The morphological, structural, thermal, rheological, and
mechanical properties of the nanocomposites were investigated. The
different modes of interaction of the polar head of the surfactant
lead to different properties. However, the global decrease in the
molecular weight of PLA, induced by the short PLLA blocks from the
surfactants and the possible degradation during melt processing, results
in a plasticization effect and impacts the crystallization of the
matrix
Supramolecular Approach for Efficient Processing of Polylactide/Starch Nanocomposites
All-biobased and
biodegradable nanocomposites consisting of polyÂ(l-lactide)
(PLLA) and starch nanoplatelets (SNPs) were prepared
via a new strategy involving supramolecular chemistry, i.e., stereocomplexation
and hydrogen-bonding interactions. For this purpose, a polyÂ(d-lactide)-<i>b</i>-polyÂ(glycidyl methacrylate) block copolymer
(PDLA-<i>b</i>-PGMA) was first synthesized via the combination
of ring-opening polymerization and atom-transfer radical polymerization.
NMR spectroscopy and size-exclusion chromatography analysis confirmed
a complete control over the copolymer synthesis. The SNPs were then
mixed up with the copolymer for producing a PDLA-<i>b</i>-PGMA/SNPs masterbatch. The masterbatch was processed by solvent
casting for which a particular attention was given to the solvent
selection to preserve SNPs morphology as evidenced by transmission
electron microscopy. Near-infrared spectroscopy was used to highlight
the copolymerâSNPs supramolecular interactions mostly via hydrogen
bonding. The prepared masterbatch was melt-blended with virgin PLLA
and then thin films of PLLA/PDLA-<i>b</i>-PGMA/SNPs nanocomposites
(ca. 600 ÎŒm) were melt-processed by compression molding. The
resulting nanocomposite films were deeply characterized by thermogravimetric
analysis and differential scanning calorimetry. Our findings suggest
that supramolecular interactions based on stereocomplexation between
the PLLA matrix and the PDLA block of the copolymer had a synergetic
effect allowing the preservation of SNPs nanoplatelets and their morphology
during melt processing. Quartz crystal microbalance and dynamic mechanical
thermal analysis suggested a promising potential of the stereocomplex
supramolecular approach in tuning PLLA/SNPs water vapor uptake and
mechanical properties together with avoiding PLLA/SNPs degradation
during melt processing
Free Radical Generation and Concentration in a Plasma Polymer: The Effect of Aromaticity
Plasma
polymer films (PPF) have increasing applications in many fields due
to the unique combination of properties of this class of materials.
Among notable features arising from the specifics of plasma polymerization
synthesis, a high surface reactivity can be advantageously used when
exploited carefully. It is related to the presence of free radicals
generated during the deposition process through manifold molecular
bond scissions in the energetic plasma environment. In ambient atmosphere,
these radicals undergo autoxidation reactions resulting in undesired
polymer aging. However, when the reactivity of surface radicals is
preserved and they are put in direct contact with a chemical group
of interest, a specific surface functionalization or grafting of polymeric
chains can be achieved. Therefore, the control of the surface free
radical density of a plasma polymer is crucially important for a successful
grafting. The present investigation focuses on the influence of the
hydrocarbon precursor type, aromatic vs aliphatic, on the generation
and concentration of free radicals on the surface of the PPF. Benzene
and cyclohexane were chosen as model precursors. First, in situ FTIR
analysis of the plasma phase supplemented by density functional theory
calculations allowed the main fragmentation routes of precursor molecules
in the discharge to be identified as a function of energy input. Using
nitric oxide (NO) chemical labeling in combination with X-ray photoelectron
spectroscopy analysis, a quantitative evaluation of concentration
of surface free radicals as a function of input power has been assessed
for both precursors. Different evolutions of the surface free radical
density for the benzene- and cyclohexane-based PPF, namely, a continuous
increase versus stabilization to a plateau, are attributed to different
plasma polymerization mechanisms and resulting structures as illustrated
by PPF characterization findings. The control of surface free radical
density can be achieved through the stabilization of radicals due
to the proximity of incorporated aromatic rings. Aging tests highlighted
the inevitable random oxidation of plasma polymers upon exposure to
air and the necessity of free radical preservation for a controlled
surface functionalization