Alkyd resins produced from bio-based resources for more sustainable and environmentally friendly coating applications.

Recently, due to the depletion of natural resources and raising environmental and economic concerns regarding petroleum derivatives, the creation of novel ecologically friendly and sustainable materials made from bio-based and renewable resources is gaining popularity. Alkyd resins are synthetic resins in which both renewable (fatty acids, glycerol, oil, etc.) and nonrenewable (maleic anhydride, pentaerythritol, phthalic anhydride, etc.) raw materials are used in their production. Due to their superior performance (good aging, greater weather resistance and high heat resistance, outstanding gloss, etc.) over other resins, easy application, low cost, and varied use, in the coating and paint industries, they are commonly used. This review covers the studies on bio-based monomers used instead of nonrenewable ones in the production of alkyds. The effects of substituted bio-based monomers on the final properties (adhesiveness, drying times, hardness, tackiness, etc.) of produced alkyds and coatings are also discussed in detail.

Polymeric Networks Derived from UV-Curing of Bio-Based Polyesters for Methyl Violet Removal.

In this study, firstly, the syntheses and characterizations of biobased polyesters with different acid values obtained from the condensation reaction of biobased itaconic acid and polyethylene glycol were investigated. Then, UV curing was applied to form polymeric networks as adsorbent material from these polyesters containing different acids. Fourier transform infrared spectrometry (FTIR), Nuclear Magnetic Resonance Spectroscopy (NMR), X-ray Photoelectron Spectroscopy (XPS), Gel Permeation Chromatography (GPC) and scanning electron microscope (SEM) were used for the characterization of polymeric networks. The effects of the parameters of contact time, initial dye concentration, pH, temperature, amount of adsorbent on adsorption were investigated by batch method. In addition, adsorption equilibrium data were analyzed by Langmuir, Freundlich, Tempkin, Elovich, Redlich-Peterson, Harkin-Jura and Jossens adsorption models. Kinetic and thermodynamic studies were performed at 298, 308, 318 and 328 K and desorption studies were also examined. Comparison studies for the effects of the acid values of the adsorbent materials on the removal of methyl violet (MV) organic pollutant from aqueous solutions were analyzed. According to the pseudo-second-order model, the adsorption capacities were found to be ≥ 357.14 mg/g for the adsorbents. From the thermodynamic data, it was determined that the mechanism was exothermic and spontaneous. As a result of the third reuse, it was found that the adsorbents had a removal efficiency of ≥ 72.36%. According to the results observed the increase in the acidities in the chemical structure of bio-based polymeric networks enhances the adsoption properties.

Preparation of rapid (chain-stopped) alkyds by incorporation of gum rosin and investigation of coating properties.

In this study, the synthesis, characterization, and properties of a short oil length chain-stopped(rapid) alkyd resin is investigated. Gum rosin modified alkyd resin (RA-GR) was prepared using soybean oil, phthalic anhydride, glycerin and gum rosin acid. An alkyd modified with benzoic acid (RA-BA) was also prepared for comparison. FTIR analyses and GPC measurements of the alkyds were used for characterization. Other properties such as the viscosity, acid value, and solid content of the final resins were determined. Separately, the synthesized resins were used in paint formulations without any changes in other parameters such as filler, airdrying agents, solvents, etc. Paints were applied to metal and glass surfaces and the effect of gum rosin was investigated by looking at touch and hard drying times, adhesion to metals and gloss changes. Compared to the benzoic acid modified resin (RA-BA), gum rosin modified resin (RA-GR) exhibited remarkable positive effects on the paint with a better adhesion to the metals, and short drying times without any loses in the glosses.

Synthesis of self-curable polysulfone containing pendant benzoxazine units via CuAAC click chemistry.

Synthesis, characterization, and properties of new thermally curable polysulfone containing benzoxazine moieties in the side chain were investigated. First, chloromethylation and subsequent azidation processes were performed to form polysulfone containing pendant clickable azide groups. Independently, antagonist 3,4-dihydro-3-(prop-2-ynyl)-2H-benzoxazine was prepared by using paraformaldehyde, phenol and propargylamine. The following copper(I) catalyzed azide-alkyne cycloaddition click reaction was applied to obtain self-curable polysulfone with pendant benzoxazine units. The polymer and intermediates at various stages were characterized by 1H-NMR, 13C-NMR and FT-IR spectroscopies. The thermal properties and curing behavior of final polymer were investigated by differential scanning calorimetry and thermal gravimetric analysis. Compared to the neat polysulfone, the obtained polymers exhibited thermally more stable polymers.

Novel axially carborane-cage substituted silicon phthalocyanine photosensitizer; synthesis, characterization and photophysicochemical properties.

The novel axially dicarborane substituted silicon (IV) (SiPc-DC) phthalocyanine was synthesized by treating silicon phthalocyanine dichloride SiPc(Cl)2 (SiPc) with o-Carborane monool. The compound was characterized by mass spectrometry, UV-Vis, FT-IR, (1)H and (11)B Nuclear Magnetic Resonance Spectroscopy (NMR). Spectral, photophysical (fluorescence quantum yield) and photochemical (singlet oxygen (ΦΔ) and photodegradation quantum yield (Φd)) properties of the complex were reported in different solutions (Dimethyl sulfoxide (DMSO), Dimethylformamide (DMF) and Toluene). The results of spectral measurements showed that both SiPc and carborane cage can have potential to be used as sensitizers in photodynamic therapy (PDT) and boron neutron capture therapy (BNCT) by their singlet oxygen efficiencies (ΦΔ=0.41, 0.39).

Photochemically prepared polysulfone/poly(ethylene glycol) amphiphilic networks and their biomolecule adsorption properties.

Polysulfone/poly(ethylene glycol) amphiphilic networks were prepared via in situ photo-induced free radical crosslinking polymerization. First, the hydrophobic polysulfone diacrylate (PSU-DA) oligomer was synthesized by condensation polymerization and subsequent esterification processes. Then, the obtained oligomer was co-crosslinked with the hydrophilic poly(ethylene glycol) diacrylate (PEG-DA) or poly(ethylene glycol) methyl ether acrylate (PEG-MA) at different feed ratios. In the case of PEG-MA, the resulting network possessed dangling pendant hydrophilic chains on the crosslinked surface. The structure and the morphology of the membranes were characterized by attenuated total reflection infrared spectroscopy (ATR-IR) and scanning electron microscopy (SEM). The enhancement of surface hydrophilicity was investigated by water contact angle measurements. The biomolecule adsorption properties of these networks were also studied. The biomolecules easily adsorbed on the surface of the hydrophobic polysulfone networks whereas dangling hydrophilic chains on the surface prevented the adsorption of the biomolecules.

Synthesis, characterization and photoinduced curing of polysulfones with (meth)acrylate functionalities.

The UV-curable telechelic polysulfones with (meth)acrylate functionalities were synthesized by condensation polymerization and subsequent esterification. The final polymers and intermediates at various stages were characterized by ¹H NMR, FT-ATR, and GPC. The oligomeric films prepared from the appropriate solutions containing these telechelics and 2,2-dimethoxy-2-phenylacetophenone (DMPA) as the photoinitiator undergo rapid polymerization upon irradiation forming insoluble networks. The photo-curing behavior was investigated by photo-DSC and the effects of the molecular weight of the polysulfone precursor and type of functionality on the rate of polymerization and conversion were evaluated. Thermal properties of the photochemically cured films were studied by differential scanning calorimeter (DSC) and thermal gravimetric analysis (TGA).

Synthesis, characterization and antimicrobial activity of water soluble dendritic macromolecules.

Several families of water soluble dendrimers were synthesized based on poly(propyleneoxide) amines (Jeffamines) (P(1)). P(1)-core and branched units were constructed from both methylacrylate and ethylenediamine (P(2)-P(9), and generations 0-3 with -NH(2), -COOH functionalities). They were characterized by elemental analysis (EA), gel permeation chromatography (GPC), FT-IR, (1)H, and (13)C NMR. The antimicrobial activities of only water soluble compounds (P(1), P(3), P(4), P(6), P(7) and P(9)) were evaluated using disk diffusion method in water as well as the minimal inhibitory concentration (MIC) dilution method against 9 bacteria. The obtained results from disk diffusion method are assessed in side-by-side comparison with those of Penicillin-g, Ampicillin, Cefotaxime, Vancomycin, Oflaxacin, and Tetracycline, well-known antibacterial agents. The results from dilution procedure are compared with Gentamycin as antibacterial and Nystatin as antifungal. The antifungal activities are reported on five yeast cultures namely, Candida albicans, Kluyveromyces fragilis, Rhodotorula rubra, Debaryomyces hansenii, and Hanseniaspora guilliermondii, and the results are referenced with Nystatin, Ketaconazole, and Clotrimazole, commercial antifungal agents. In most cases, the compounds show broad-spectrum (gram-positive and gram-negative bacteria) activities that are comparatively higher or equipotent to the antibiotic and antifungal agents in the comparison tests.