Influence of nanoclay on urea–glyoxalated lignin–formaldehyde resins for wood adhesive

In this research, the influence of nanoclay on urea–glyoxalated lignin–formaldehyde (GLUF) resin properties has been investigated. To prepare the GLUF resin, glyoxalated soda baggase lignin (15 wt%) was added as an alternative for the second urea during the UF resin synthesis. The prepared GLUF resin was mixed with the 0.5%, 1%, and 1.5% nanoclay by mechanically stirring for 5 min at room temperature. The physicochemical properties of the prepared resins were measured according to standard methods. Then the resins were used in particleboard production and the physical and mechanical properties of the manufactured panels were determined. Finally, from the results obtained, the best prepared resin was selected and its properties were analyzed by differential scanning calorimetry (DSC), Fourier transform infrared spectrometry (FTIR), and X-ray diffractometry (XRD). Generally the results indicated that the addition of sodium-montmorillonite (NaMMT) up to 1.5% appears to improve the performance of GLUF resins in particleboards. The results also showed that nanoclays improved mechanical strength (modulus of elasticity (MOE), Modulus of Rupture (MOR), and internal bond (IB) strength) of the panels bonded with GLUF resins. The panels containing GLUF resin and nanoclay yielded lower formaldehyde emission as well as water absorption content than those made from the neat GLUF resins. XRD characterization indicated that NaMMT only intercalated when mixed with GLUF resin. Based on DSC results, the addition of NaMMT could accelerate the curing of GLUF resins. The enthalpy of the cure reaction (ΔH) of GLUF resin containing NaMMT was increased compared with neat GLUF resin. Also the results of FTIR analysis indicated that addition of NaMMT change the GLUF resins structures.     

The effect of soda bagasse lignin modified by ionic liquids on properties of the urea–formaldehyde resin as a wood adhesive

The aim of this research was to investigate the influence of lignin modified by ionic liquids on physical and mechanical properties of plywood panels bonded with the urea–formaldehyde (UF) resin. For this purpose, soda bagasse lignin was modified by the 1-ethyl-3-methylimidazolium acetate ([Emim][OAc]) ionic liquid and then the various contents of unmodified and modified lignins (10, 15, and 20%) were added at pH=7 instead of second urea during the UF resin synthesis. The physicochemical properties of the prepared resins as well as the water absorption, shear strength, and formaldehyde emission of the plywood panels made with these adhesives were measured according to standard methods. According to Fourier Transform Infrared (FTIR) Spectrometry, by treatment of lignin, the C=O, C–C, and C–H bonds decrease while the content of the C–N bond dramatically increases. Based on the finding of this research, the performance of soda bagasse lignin in UF resins dramatically improves by modification by ILs; as the resins with modified lignin yielded lower formaldehyde emission and water absorption when compared to those made from unmodified lignin and commercial UF adhesives, respectively. The shear strength as well as wood failure percentages are lower for the panels produced with modified lignin than for the panels produced with UF resins alone.     

Hydrothermal synthesis of Co3O4 nanosheets and its application in photoelectrochemical water splitting

In this study, Co₃O₄ nanosheets were synthesized through hydrothermal method using cobalt nitrate hexahydrate. X-ray diffraction, diffuse reflectance spectra, Fourier transform infrared spectroscopy, energy-dispersive X-ray spectroscopy, and field emission scanning electron microscopy were applied to investigate the properties of as-synthesized samples. Ultimately, the electrochemical and photoelectrochemical properties were evaluated by Mott–Schottky analysis and measuring photoconversion efficiency of Co₃O₄ nanosheets. The results indicated that Co₃O₄ nanosheets exhibited a maximum efficiency of 0.92% for water electrolysis under simulated 1.5 global sunlight air mass, which further suggests the excellent potential of Co₃O₄ nanosheets for application in hydrogen generation through photocatalytic water splitting.     

Ionic liquid modified lignin-phenol-glyoxal resin: a green alternative resin for production of particleboards

The aim of this research was to evaluate the properties of particleboard panels bonded with ionic liquid treated lignin- phenol- glyoxal (LPG) resin. For this purpose, soda bagasse lignin was modified by 1-ethyl-3-methylimidazolium acetate ([Emim][OAc]) ionic liquid and then various contents of virgin and modified lignin (20, 30 and 40 wt% based on weight of phenol), phenol and glyoxal were used for synthesis of LPG resins. After resin synthesis, thermal and physicochemical properties of the synthesized resins such as curing behavior, gelation time, viscosity, solid content and density were measured. Finally, the resins so prepared were used for laboratory particleboard manufacturing. The panels physical (water absorption, thickness swelling) as well as mechanical (MOE, MOR and internal bond strength) properties were measured according to standard methods. The resins tests indicated that modification of lignin with ionic liquid not only can accelerate the gelation time and increase viscosity, density and solid content of LPG resins but also decrease the temperature required for curing the LPG resins. Based on the results of this work, the mechanical strength and dimensional stability of the particleboards bonded with a LPG resin can be improved by using modified lignin. The particleboards prepared with the LPG resin, using either modified or virgin lignin, presented higher water absorption as well as weaker mechanical strength than those prepared with the control PF resin. However, there does not appear to be any statistically significant difference between the some properties of the panels bonded with the control PF resin and those bonded with the LPG resin containing modified lignin.     

Fourier transform infrared spectroscopic and AC electrical conductivity studies of chitin and its derivatives

The vibrational modes and the purity index of chitin and its derivatives as biopolymers are studied by Fourier transform infrared spectroscopy in the wavenumber range from 4000 to 400 cm^?1. The absorption bands of chitin and its derivatives are assigned. New bands appeared at 1419, 1209, 915, and 800 cm^?1 for chitin derivatives due to the change of vibrational modes. The purity indexes are calculated from the ratio of the absorption band of C = O at 1662 cm^?1 and OH at 3443 cm^?1. Generally, the purity indexes of chitin derivatives are higher than that of chitin, which is due to the decrease of OH. The dielectric properties such as the real part of the dielectric constant (ε′) and loss tangent tan (δ) are measured as a function of temperature at different frequencies ranging from 200 to 2000 kHz. The increase of (ε′) and tan (δ) with increasing temperature is discussed on the basis of increasing polarizability and the decrease with increasing frequency can be attributed to the dielectric dispersion. AC electrical conductivities as a function of the reciprocal of the absolute temperature are also discussed. The mechanism of the charge carrier is discussed as a tunneling model in the temperature range from 300 to 360 K. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 936–943, 2005     

Application of mesoporous magnetic carbon composite for reactive dyes removal: Process optimization using response surface methodology

Discharging the effluents of textile wastewaters into potable water resources can endanger the ecosystem, due to their reactivity, toxicity, and chemical stability. In this research, the application of powder activated carbon modified with magnetite nanoparticles (PAC-MNPs) as an adsorbent for removal of reactive dyes (Reactive black 5 (RB5) and reactive red 120 (RR120)) was studied in a batch system. The adsorption performance was evaluated as a function of temperature, contact time and different adsorbent and adsorbate concentrations. The levels of factors were statistically optimized using Box-Behnken Design (BBD) from the response surface methodology (RSM) to maximize the efficiency of the system. The adsorption process of both dyes was fit with the pseudo-second order kinetic and Langmuir isotherm models. The identified optimum conditions of adsorption were 38.7 °C, 46.3 min, 0.8 g/L and 102 mg/L for temperature, contact time, adsorbent dose, and initial dyes concentration, respectively. According to the Langmuir isotherm, the maximum sorption capacities of 175.4 and 172.4 mg/g were obtained for RB5 and RR120, respectively. Thermodynamics studies indicated that the adsorption process of the reactive dyes was spontaneous, feasible, and endothermic. After five cycles, the adsorption efficiency was around 84 and 83% for RB5 and RR120, respectively. A high value of desorption was achieved, suggesting that the PAC-MNPs have a good potential in regeneration and reusability, and also can be effectively utilized in industrial applications. PAC-MNPs also show a good anti-interference potential for removal of reactive dyes in dye-industry wastewaters.     

Characterization of mechanically sheared edges of dual phase steels

In recent years advanced high strength steels (AHSS) received increased interest for light structures with improved performance, but they are often sensitive to edge cracking during sheet metal forming. In this study mechanically sheared edges were characterized for three dual phase steels (DP600, DP780 and DP980), sheared with three die clearances (5%t, 10%t, 15%t) and along rolling and transverse directions. Microstructures of the materials were provided first, and then the sheared edges were examined by optical microscopy and scanning electron microscopy that reveal the morphology and random feature of the sheared edges. A factorial analysis was performed to reveal the general trends of the processing parameters on four edge zones. A new strain measurement method was used for characterizing strain distribution in the sheared region, which shows the peak strain to be higher than 3. The strain quickly decreases from sheared edge to interior, leaving a shear-affected zone of about 500 μm or 31% of the thickness. The fracture processes and involved mechanisms were discussed.     

Direct Polyamidation in Molten Tetrabutylammonium bromide: Novel and Efficient Green Media

This is the first report of application of molten ionic liquid (MIL) for the synthesis of polyamides (PAs) from the reaction of dicarboxylic acids with diisocyanates. A fairly inexpensive and readily accessible MIL, tetrabutylammonium bromide (TBAB) was used for the synthesis of polymers. Therefore, polycondensation of terephthalic acid with various commercially available diisocyanates was performed in molten TBAB with or without dibutyltin dilaurate (DBTDL) as a catalyst. The polymerization reaction gave similar results in the presence or absence of DBTDL, indicating that, the catalyst was not needed in this process. Various PAs were obtained with high yields and moderate inherent viscosities ranging from 0.36 to 0.71 dL/g. This method was compared with the polymerization reaction in conventional solvent and in the presence of DBTDL as a catalyst. In the case of using TBAB, higher yields and inherent viscosities were obtained. This process is safe and green since toxic and volatile organic solvent such as N-methylpyrrolidone (NMP) was eliminated.     

Platinum(VI) dihydroxo tetramesitylporphyrin; characterization and chemical reactivity

Tetramesitylporphyrin platinum(VI) dihydroxo complex, TMPPt(OH)₂ · 2 benzoate was synthesized by addition of two equivalent of meta-chloroperbenzoic acid molecules to the tetramesitylporphyrin platinum(II). This complex was characterized by X-ray diffraction and spectroscopic methods, and is capable to convert two molecules of triphenylphosphine to triphenylphosphine oxide.     

Microstructural Characterization and Mechanical Properties of Si3N4 Formed by Fused Deposition of Ceramics

We present processing (green and sintered), part shrinkage and warping, microstructural characterization, and mechanical properties of Si₃N₄ made by fused deposition of ceramics (FDC), using optical microscopy, scanning electron microscopy, and X-ray diffraction. The mechanical properties (fracture strength, fracture toughness, and Weibull modulus) are also reported. Proper FDC build parameters resulted in dense, homogeneous, near-net-shape Si₃N₄, with microstructures and mechanical properties similar to conventionally processed material. Mechanical properties are shown to be isotropic, while there is some degree of microstructural texturing (preferred β-Si₃N₄ grain orientation) in sintered components.