On the compatibility of the IPP/PA6/EPDM blends with and without functionalized IPP I. Thermo-oxidative behaviour

Binary isotactic polypropylene (IPP)/polyamide 6 (PA6) and ternary IPP/PA6/ethylene–propylene diene terpolymer (EPDM) blends in various ratios were obtained in a Haake Rheocord mixer. Processing behaviour was changed in the presence of IPP functionalized with bismaleimide (BMI), maleic anhydride (MA) and acrylic acid (AA) as reactive compatibilizing agents. The thermal and thermo-oxidative behaviour of blends was studied by differential scanning calorimetry and thermogravimetry. The functionalized IPPs modify the crystallinity degree and the decomposition behaviour of both IPP and PA6 as a result of chemical reactions of functional groups with those of the PA6. The changes depend on the IPP/PA6 or IPP/PA6/EPDM ratio, the chemical nature and amount of the functionalized IPP. On the basis of the processing and thermal data one can conclude that the compatibilizing agent effect increases in the following order: IPP-AA 相似文献   

Thermo-oxidative degradation of some elastomers with a high content of 3,4 isoprene units

New elastomers with high content of 3,4 isoprene units have been developed during the last decades in an attempt to ensure superior performances of the final products and the present study is devoted to the investigation of some peculiarities of their ageing behaviour. On thermo-oxidative degradation, 3,4 isoprene units are less affected in comparison to cis-1, 4 and trans-1, 4 isoprene units. The degradation process consists mainly in splitting of the main chains at temperatures of 80–100 °C while at higher temperatures (120–130 °C) branching becomes a significant modification and this reaction is enhanced for the polymers containing preponderantly 3,4 units. Such behaviour leads to the fact that the processability of polymers containing high amounts of 1,2 and 1,3 isoprene units is less affected by thermo-oxidative degradation in comparison with cis-1, 4-polyisoprene, which could be explained by the fact that large amounts of double bonds are not present in the backbone of macromolecules but in the pendent groups.     

Hexachloroantimonate(V) mit Nitroderivaten als Liganden, 3. Mitt.: Komplexe Verbindungen mit dreiwertigen Metallen

Complex compounds of trivalent metal chlorides (AlCl₃, CrCl₃, FeCl₃) are described, which had been obtained in a double complexation reaction in CCl₄ as a solvent with nitro compounds and SbCl₅:M ^III(C₆H₅NO₂) _m (SbCl₆)₃ (m=3,6),M ₂ ^III(C₆H₅NO₂)₄(SbCl₆)₄ and Al(-C₁₀H₇NO₂)₃(SbCl₆)₃. Synthesis, analytical results and i.r. spectra are discussed.     

Bioactive Co(II), Ni(II), and Cu(II) Complexes Containing a Tridentate Sulfathiazole-Based (ONN) Schiff Base

New Co(II), Ni(II), and Cu(II) complexes were synthesized with the Schiff base ligand obtained by the condensation of sulfathiazole with salicylaldehyde. Their characterization was performed by elemental analysis, molar conductance, spectroscopic techniques (IR, diffuse reflectance and UV–Vis–NIR), magnetic moments, thermal analysis, and calorimetry (thermogravimetry/derivative thermogravimetry/differential scanning calorimetry), while their morphological and crystal systems were explained on the basis of powder X-ray diffraction results. The IR data indicated that the Schiff base ligand is tridentate coordinated to the metallic ion with two N atoms from azomethine group and thiazole ring and one O atom from phenolic group. The composition of the complexes was found to be of the [ML₂]∙nH₂O (M = Co, n = 1.5 (1); M = Ni, n = 1 (2); M = Cu, n = 4.5 (3)) type, having an octahedral geometry for the Co(II) and Ni(II) complexes and a tetragonally distorted octahedral geometry for the Cu(II) complex. The presence of lattice water molecules was confirmed by thermal analysis. XRD analysis evidenced the polycrystalline nature of the powders, with a monoclinic structure. The unit cell volume of the complexes was found to increase in the order of (2) < (1) < (3). SEM evidenced hard agglomerates with micrometric-range sizes for all the investigated samples (ligand and complexes). EDS analysis showed that the N:S and N:M atomic ratios were close to the theoretical ones (1.5 and 6.0, respectively). The geometric and electronic structures of the Schiff base ligand 4-((2-hydroxybenzylidene) amino)-N-(thiazol-2-yl) benzenesulfonamide (HL) was computationally investigated by the density functional theory (DFT) method. The predictive molecular properties of the chemical reactivity of the HL and Cu(II) complex were determined by a DFT calculation. The Schiff base and its metal complexes were tested against some bacterial strains (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus subtilis). The results indicated that the antibacterial activity of all metal complexes is better than that of the Schiff base.     

Phosphonate mediated surface reaction and reorganization: implications for the mechanism controlling cement hydration inhibition

Vertical scanning interferometry and XPS show the reaction of CaCO3 with the hydration retarder nitrilo-tris-(methylene)phosphonic acid follows a pathway of dissolution of the calcium followed by precipitation of a calcium phosphonate; subsequent surface reorganization/restructuring of the calcium phosphonate exposes the underlying CaCO3 for further hydration.     

New Nucleic Base-Tethered Trithiolato-Bridged Dinuclear Ruthenium(II)-Arene Compounds: Synthesis and Antiparasitic Activity

Aiming toward compounds with improved anti-Toxoplasma activity by exploiting the parasite auxotrophies, a library of nucleobase-tethered trithiolato-bridged dinuclear ruthenium(II)-arene conjugates was synthesized and evaluated. Structural features such as the type of nucleobase and linking unit were progressively modified. For comparison, diruthenium hybrids with other type of molecules were also synthesized and assessed. A total of 37 compounds (diruthenium conjugates and intermediates) were evaluated in a primary screening for in vitro activity against transgenic Toxoplasma gondii tachyzoites constitutively expressing β-galactosidase (T. gondii β-gal) at 0.1 and 1 µM. In parallel, the cytotoxicity in non-infected host cells (human foreskin fibroblasts, HFF) was determined by alamarBlue assay. Twenty compounds strongly impairing parasite proliferation with little effect on HFF viability were subjected to T. gondii β-gal half maximal inhibitory concentration determination (IC₅₀) and their toxicity for HFF was assessed at 2.5 µM. Two promising compounds were identified: 14, ester conjugate with 9-(2-oxyethyl)adenine, and 36, a click conjugate bearing a 2-(4-(hydroxymethyl)-1H-1,2,3-triazol-1-yl)methyl substituent, with IC₅₀ values of 0.059 and 0.111 µM respectively, significantly lower compared to pyrimethamine standard (IC₅₀ = 0.326 µM). Both 14 and 36 exhibited low toxicity against HFF when applied at 2.5 µM and are candidates for potential treatment options in a suitable in vivo model.     

Electrochemical and microgravimetric studies of poly[3,4-ethylenedioxythiophene]-tyrosinase biocomposite material electrodeposited onto gold electrodes by a sinusoidal voltages method

The electrodeposition of poly(3,4-ethylenedioxythiophene)-tyrosinase (PEDOT-Ty) biocomposite material onto gold electrode has been achieved by means of a sinusoidal voltages (SV) method. The SV method consists in the superimposition of a sinusoidal voltage (sin wave) with fixed frequency and amplitude onto a d.c. potential. The influence of electrochemical parameters like frequency and amplitude of SV signal, d.c. potential value, deposition time, on the electrodeposition process has been investigated. The biocomposite material has been prepared as a thin layer onto quartz crystals coated with gold. The frequency change of the quartz crystal during the electrodeposition of the biocomposite material was recorded simultaneously with the measured current response. The morphology of the deposited PEDOT-Ty coatings was investigated by scanning electron microscopy. The electrochemical behavior of the biocomposite material in aqueous solution was studied by cyclic voltammetry and electrochemical impedance spectroscopy. The use of d.c. potential value of 0.6 V revealed the contribution of the SV component to the electrodeposition process. The PEDOT-Ty modified electrode was used as an electrochemical biosensor in the voltammetric determination of dopamine in the presence of hydroquinone. The analytical performances of the prepared biosensors were also investigated.     

On univalence of two integral operators

In this work we consider two integral operators. The integral operators were constructed on the basis of the fact that the number of functions from the composition of the operators is the entire part of a complex number modulus.