Residual stability of polyurethane automotive coatings measured by chemiluminescence and equivalence of Xenotest and Solisi ageing tests

Degradation of poly(ester-urethanes) and poly(acrylic-urethanes), as a base for automotive paintings in interior applications, has been studied by chemiluminescence. The samples were clearcoat and black-pigmented paints, unstabilised and stabilized with HALS Tinuvin 292 and UV absorber Tinuvin 1130, exposed to various doses of artificial weathering in Xenotest and Solisi equipment. Chemiluminescence has appeared a powerful tool to evaluate the oxidation stability of various polyurethane systems. From the dependences of oxidation onset temperature on heating rate, the kinetic parameters describing the dependence of induction periods on temperature have been obtained. The kinetic parameters enabled us to calculate the length of the induction period for a chosen temperature, the protection factors of various additives and the residual stability of the polymer after an artificial ageing stress. It has been found that the loss of residual stability with ageing dose obeys a first-order relationship. Equivalence between the two methods of artificial ageing has been determined. The results indicate that the equivalence depends on the polymer composition. The procedure presented here can also be applied for the determination of equivalence of accelerated and field tests so contributing to establishing a reliable correlation between them.     

Physicochemical and antibacterial properties of polyurethane coatings modified by ZnO

The synthesis of polyurethane nanocomposite coatings containing 1% to 5% suitably dispersed ZnO by 1‐stage polyaddition process in the bulk using 4,4′‐methylenebis(cyclohexyl isocyanate), poly(ε‐caprolactone)diol, and 1,4‐butanediol was performed. Infrared and nuclear magnetic resonance spectra confirmed the structure of obtained polyurethanes. Scanning electron microscope and energy dispersive X‐ray analyzer methods showed randomly distributed ZnO in a polyurethane matrix. The differential scanning calorimetry and wide‐angle X‐ray diffraction patterns were used for the microstructural assessment of the obtained materials. Antimicrobial properties of ZnO and the effect of this modifier on the hydrophobicity of the coatings were demonstrated. The obtained coatings were characterized in terms of the mechanical properties and changes during incubation in a Baxter saline solution.     

Thermal stability evaluation of doping compounds before GC-MS analysis by DSC

The Medical Commission of the International Olympic Committee forbids the use of anabolic androgenic steroids, β-agonists, stimulant and narcotic compounds to improve athletic performance. In this work, we evaluated the thermal stability of 17 compounds by the use of the DSC for their potential GC-MS analysis either under free form or under TMS derivative form. In DSC, esterified and unesterified anabolic steroids were characterized by a true melting peak, followed by a large exothermic peak at about 251–316°C due to oxidative degradation. They could be analysed by GC-MS mainly under TMS derivatives. Hydroxylated and unhydroxylated stimulant compounds (xanthines) seemed to be more stable at high temperature. As unhydroxylated xanthines were not silylated with BSTFA - TMCS, their GC analysis would be done under their free forms. TMS derivatisation of albuterol hemisulfate and codeine phosphate is preferable. In our conditions, to analyse by GC-MS all 17 doping compounds in the same GC-MS run, the optimal silylation temperature and best column initial temperature were determined at both 60°C.     

Use of chemiluminescence to the study of photostability of automotive coatings

Chemiluminescence (CL) imaging has been used to study the photodegradation of two automotive coatings, a melamine-crosslinked acrylic resin and an acrylic Polyurethane, as a function of artificial weathering time. Characteristics of the CL emission from coatings, the influence of light stabilizers and different types of sample were studied. The results indicate that the method is highly sensitive and can be used to measure photodegradation in unstabilized and stabilized coatings after only 48 h and 100–200 h of exposure, respectively. Measurements can be carried out on free clearcoats or on clearcoats applied on metallic panels. It is also possible to assess the degradation of individual layers in multiple-layer coating systems. Extrapolation to the failure time of coatings by CL is not yet achievable, but results show that the technique is useful for rapidly screening the relative performance of new coating formulations or light stabilizers added to clearcoats.     

Thermal stability of bovine serum albumin DSC study

A calorimetric study of thermal denaturation of bovine serum albumin in aqueous solutions has shown essential differences in stability of fatty acid containing and defatted albumin. The first one shows a single endotherm peak in DSC curve near 69°C with enthalpy change about 1000 kJ mol^-1. Defated albumin melts in two different temperature ranges: near 56 and 69°C with enthalpy changes about 300 and 200 kJ mol^-1 respectively. Deconvolution analysis shows that the single endotherm is well approximated as the sum of three independent two-state transitions. Two transitions of bimodal DSC curve for defatted albumin are not of a two-state type. This molecule melts probably as two structurally independent parts. This revised version was published online in July 2006 with corrections to the Cover Date.     

Surface free energy of polyurethane coatings with improved hydrophobicity

The polarity of polyurethane coats was studied on the basis of the goniometric method for determination of wetting angle values, on the basis of calculated surface free energy (SFE) values by the van Oss-Good and Owens-Wendt methods, and on the basis of polarity measurements with the use of the (1)H NMR spectra. Test polyurethanes were synthesised in the reaction of methylene diphenyl 4,4'-diisocyanate (MDI) or 3-izocyanatomethyl -3,5,5- trimethylcyclohexyl isocyanate (IPDI) and polyoxyethylene glycols or polyesters poly(ε-caprolactone) diols and poly(ethyleneadipate) diol with different molecular weights, and some diols as chain extenders, in dioxane. The type of raw material was found to significantly affect the phase structure of the obtained polyurethane elastomers and to control physical interactions within those structures, thus influencing the SFE values. Fundamental reduction in the SFE value of a coating below 28?mJ/m(2) was achieved by the use of 2,2,3,3-tetrafluoro-1,4-butanediol as the urethane prepolymer chain extender.     

Synthesis and characterization of hyperbranched polyesters and polyurethane coatings

Polyurethane (PU) coatings are widely used for variety of high‐performance applications in today's coating technology. The emerging hyperbranched polymers having three‐dimensional morphology have opened a new avenue to tailor the architecture of PU coatings. The methodology followed here is based on preparation of PU coatings from hyperbranched polyester. Initially, different hyperbranched polyester polyols (HPs) were synthesized by varying the hydroxyl‐terminated precursors that is, pentaerythritol, trimethylol propane or glycerol and keeping the diacid that is, adipic acid quantity constant at various mole ratios of 1:0.6, 1:0.8, 1:0.9, and 1:1, respectively. The obtained HPs were characterized by nuclear magnetic resonance (NMR) spectroscopy, matrix‐assisted laser desorption/ionization time‐of‐flight (MALDI‐TOF)‐mass spectrometry, and Fourier transform‐infrared (FTIR) spectroscopy. The degree of branching and the quantity of different structural units present in the various HPs were calculated by integrating the quaternary carbon and carbonyl zone in ¹³C NMR spectroscopy. The extent of condensation in different HPs was also calculated from ¹H NMR spectra. Later on, NCO‐terminated PU prepolymers (NCO‐PU) were synthesized by reacting HPs with isophorone diisocyanate (IPDI) at NCO/OH ratio of 1.6:1. In the third step, the excess NCO content in the NCO‐capped PU prepolymers were reacted with atmospheric moisture and hyperbranched polyurethane (HPU) coatings were formed. The coating films were analyzed by FTIR and dynamic mechanical thermal analysis instruments. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 2673–2688, 2007     

Effects of spice extracts on lipid fraction oxidative stability of cookies investigated by DSC

The addition of natural antioxidants to the bakery products containing fats can extend their shelf life, and it may be more attractive to consumers. In this research, the antioxidant effect of spice extracts and synthetic antioxidant on oxidative stability of fat extracted from cookies was evaluated by differential scanning calorimetry (DSC). The results revealed that addition of spice extracts to the cookies in comparison to cookies without additives reduced the oxidation as evidenced by higher the onset oxidation temperature (t _ON) of antioxidant-treated samples. Using the Ozawa–Flynn–Wall method, the activation energies (E _a/kJ mol^?1) and pre-exponential factors (Z/min^?1) and then induction times (τ/min) were calculated and also used for evaluation of antioxidants efficiency. After baking, cookies were also subjected to sensory studies and to instrumental measurements of colour changes. Among the samples studied, cookies with 0.02 % of rosemary or 0.2 % thyme extracts showed good sensorial acceptability. Cookies fortified with spice extracts also characterised greater lightness compared to the control sample.     

Evaluation of thermodynamic properties of irreversible protein thermal unfolding measured by DSC

Summary We assessed the applicability of the extrapolation procedure at infinite scanning rate to differential scanning calorimetry (DSC) data related to irreversible protein unfolding. To this aim, an array of DSC curves have been simulated on the basis of the Lumry-Eyring model N↔U→F. The results obtained confirmed that when the apparent equilibrium constant K_{app (T=T1/2)} is lower than 3, the application of the extrapolation procedure provides accurate thermodynamic parameters. Although this procedure applies only to monomeric proteins for which the Lumry-Eyring model is a reasonable approximation, it will hopefully contribute to increase the potential of DSC in obtaining reliable thermodynamic information regarding the folding/unfolding equilibrium.     

Improvement of the thermo-oxidative stability of low-density polyethylene films by organic-inorganic hybrid coatings

LDPE films have been coated with single or bi-layer hybrid coatings formed through sol-gel reactions in order to improve their thermo-oxidative resistance. Different chemical compositions of the coating were investigated which differ either in the amount of the inorganic phase (silica deriving from tetraethoxysilane) or in the organic component (either alkoxy silane functionalized polyethylene-poly(ethylene glycol) diblock copolymers or poly(vinyl alcohol)). The thermo-oxidative stability of the coated films thus obtained has been assessed by means of isothermal differential scanning calorimetry (DSC) and isothermal thermo-gravimetric analysis (TGA) under accelerated conditions, i.e. at high temperatures in pure oxygen flow. Conventional ageing in air at lower temperature, slightly above the in-service one, has also been carried out. The obtained data show: a) a general improvement of the thermal-resistance for the coated LDPE samples; b) a particularly high thermal-resistance for LDPE coated with a bi-layer coating with pure silica in the top layer; c) the effectiveness of the accelerated techniques in qualitatively assessing the thermo-oxidative resistance of the coated polymeric systems.     

Synthesis and thermal properties of soybean oil-based waterborne polyurethane coatings

Waterborne polyurethane coatings were prepared by a polyaddition reaction using toluene diisocyanate (TDI), 2,2-di(hydroxy-methyl) propionic acid, soy-based polyols with different hydroxyl values, plus 2-hydroxyethyl methacrylate (HEMA) as chain termination agent, triethylamine as neutralization agent, and DBTDL as catalyst. Six soybean oil-based polyols were used in this study with hydroxyl values of 100, 115, 128, 140, 155, and 164 mg KOH g⁻¹, respectively. The molar ratio of polyol hydroxyl to DMPA was varied from 1.6 to 2.6. The storage stability of the waterborne polyurethane coatings was greater than 6 months. The thermal properties of the coating films were investigated by TG and DCS. The results show that the soy-based polyurethane films decomposed in three stages. The glass transition temperatures, T _g, of the soy-based polyurethane films increased with the hydroxyl number of the soy-based polyol.     

Influence of containing moisture on hydrothermal stability of modified collagen thermal characteristics analysis by DSC

The thermal stability of sheepskin collagen cross-linked with chrome sulfate and mimosa (MI)–oxazolidine (OZ), respectively, had been researched in this experiment. All samples’ shrinkage temperatures (T _s) are determined by a special T _s-testing-apparatus and denaturation temperatures (T _d) are determined by the differential scanning calorimetry. The relations between the modified collagens containing moisture and their hydrothermal stability, T _s or T _d, were studied. The results show that the cross linking agents can enhance the thermal stability of modified collagen whose T _s are 109.8 and 110.6 °C for collagen treated with chrome and MI–OZ, respectively. When the samples contain 25–71.9% moisture for chrome leather and 20–71.1% for leather treated with MI–OZ, the hydrothermal stability will decrease with the increase of moisture. It was found that the difference between T _s and T _d of collagen modified by chrome is more obvious than that of collagen modified with MI–OZ. And when the moisture of chrome leather exceeds 55%, T _d cannot express thermal stability of modified collagen as a substitute for T _s, and the moisture is 40% for leather tanned with MI–OZ.     

DSC study of the deposition reactions of zinc pack coatings up to 550°C

Zn pack coating formation takes place in three steps as differential scanning calorimetry shows. The initial step (at 193.9°C) is endothermic and involves the transformation of α-NH₄Cl to β-NH₄Cl and the NH₄Cl decomposition to NH₃ and HCl. During the second step (at 248.6°C), which is exothermic, Zn²⁺ salts are formed and most probably ZnCl₂. Finally at 264.1°C (endothermic reaction) it seems that ZnCl2 is decomposed to form Zn that is deposited on the ferrous substrate. The as-cast Zn diffuses in the iron substrate forming the gamma and delta phase of the Fe–Zn phase diagram. Al₂O₃ is not involved in the above-mentioned mechanism and acts only as filler.     

Application of the DSC analysis of thermoplastic polyurethane elastomers to a comparative study of their technological properties

The fusion and crystallization enthalpies, dynamic viscosity of melts and tensile properties of a series of commercially available thermoplastic polyurethane elastomers (TPU) were estimated. The DSC analysis has been proved as useful to prediction of the processability and tensile properties of TPU's with a similiar hard segment content.

---

Zusammenfassung Schmelz- und Erstarrungsenthalpie, die dynamische Viskosität der Schmelze und Zugdehnungseigenschaften bei einer Reihe von im Handel erhältlichen thermoplastischen Polyurethanelastomere (TPU) wurden ermittelt. DSC-Anaiyse erwies sich als ein geeignetes Mittel zur Vorhersage der Verarbeitungsfähigkeit und der Zugdehnungseigenschaften von TPU mit ähnlichem Hartsegmentanteil.

     

Oxidation stability of polymeric materials dynamic DSC/DTA method

The dynamic DSC/DTA method was observed to give better selectivity and reproducibility than the isothermal method when estimating relative oxidation stability of plastics materials. The dynamic DSC/DTA method is in this survey exposed to a round robin test. Results of various instruments and test stations are compared, and their compatibility is unexpectedly good. Subsequently the dynamic DSC/DTA method was chosen as the quality control method and will be published as Finnish standard SFS 3449.

---

Zusammenfassung Bei der Bestimmung der relativen Oxydationsbeständigkeit plastischer Materialien wurden mit der dynamischen DSC/DTA-Methode eine bessere Selektivität und Reproduzierbarkeit als mit der isothermen Variante beobachtet. Die dynamische Methode wurde in verschiedenen Laboratorien getestet. Die mit verschiedenartigen Geräten in verschiedenen Laboratorien erhaltenen Testergebnisse stimmen überraschend gut überein. Die dynamische DSC/DTA-Methode wurde deshalb als Qualitätskontrollmethode gewählt und wird als finnische Norm SFS 3449 herausgegeben.

---

, / , . . , . , . / SFS 3449.

---

---

Thanks are due to the Finnish Plastics Industries Federation and its member companies for the helpful interest in the course of this survey.     

New aromatic oligoesters and their use in the synthesis of heat-resistant polyurethane coatings

For manufacturing new varnish polyurethane coatings with high hardness and elasticity at maintaining adhesion and strength properties oligoester diols were synthesized based on hydroxyethylated diphenylpropane derivatives and aromatic dicarboxylic acids.