Photocatalytic degradation and heat reflectance recovery of waterborne acrylic polymer/ZnO nanocomposite coating

This work aims to clarify the photocatalytic degradation mechanism and heat reflectance recovery performance of waterborne acrylic polymer/ZnO nanocomposite coating. To fabricate the nanocomposite coating, ZnO nanoparticles (nano-ZnO) were dispersed into acrylic polymer matrix at the various concentrations from 1 to 6% (by total weight of resin solids). The photocatalytic degradation of nanocomposite coating under ultraviolet (UV) light irradiation has been investigated by monitoring its weight loss and chemical/microstructural/morphological changes. As the topcoat layer, its heat reflectance recovery has been evaluated under UV/condensation exposure by using an artificial dirty mixture of 85 wt% nanoclay, 10 wt% silica particles (1–5 μm), 1 wt% carbon black, and 2 wt% engine oil. After 108-cycle UV/condensation exposure, infrared spectra and weight loss analysis indicated that the maximal degradation for nanocomposite coating is observed at 1 wt% nano-ZnO. On the other hand, after 96 hr of UV light exposure, the nanocomposite coating with1 wt% nano-ZnO could restore effectively the reflective index of solar-heat reflectance coating (from 58.45 to 80.78%). Finally, the photodegradation mechanism of this waterborne acrylic polymer coating has been proposed as the UV-induced formation of CC CO conjugated double bonds. As a result, its self-cleaning phenomenon can be achieved as the recovery of heat reflectance.     

Simple preparation of ordered mesoporous carbons assisted by an organosilicate as a linking material

Ordered mesoporous carbon materials (OMCs) were prepared from a silica–carbon composite assisted by 3-mercaptopropyltrimethoxysilane (MPTMS) in an aqueous phase. The obtained OMCs have a high surface area, large pore volume and uniform pore structure. MPTMS plays an important role in linking the polymer part with silica part to form a mesoporous structure. Importantly, the amount of MPTMS used is an important determinant in the development of a uniform mesoporosity. The method described herein has some important advantages over existing methods, such as simplified synthesis steps for the preparation of OMCs, the fact that the aqueous phase can be used and that the resulting materials have a high surface area of more than 1700 m²/g.     

Epoxy resins toughened with in situ azide–alkyne polymerized polysulfones

To simultaneously improve the fracture toughness and heat resistance of a cured toughened epoxy resin along with a reduction in its viscosity during the mixing process, two novel polysulfone‐type polymers are synthesized via azide–alkyne polymerization for use as toughening agents. The epoxy resin toughened with these polymers by in situ azide–alkyne polymerization during the cure process, which shows excellent processibility and based on the significantly lower viscosity (61 and 62 cP) during epoxy mixing process than that of commonly commercial polyethersulfone (PES, 127,612 cP). The novel polysulfone‐type polymer toughened epoxy resin showed the advantage in excellent fracture toughness than the PES toughened epoxy. In addition, the glass transition temperature of the novel polysulfone‐type polymer toughened epoxy resin is similar to that of the neat one (～230 °C) and does not decrease, which implies excellent heat resistance of the toughened epoxy. These phenomena can be attributed to the formation of semi‐interpenetrating polymer networks comprising the epoxy network and the linear polysulfone‐type polymers. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45790.     

Oxidative decomposition of naphthalene by supported metal catalysts

A fixed-bed reactor was utilized to investigate the activities of six metal catalysts (1% Pt, 1% Pd, 1% Ru, 5% Co, 5% Mo and 5% W on γ-Al₂O₃ support) in decomposing naphthalene, based on the production of carbon dioxide and the disappearance of naphthalene. The Pt and Pd catalysts were found to exhibit higher naphthalene oxidizing activity than other catalysts tested. The Co catalysts, whose activity is similar to that of the Ru catalysts, are promising for naphthalene oxidation. The kinetic results of naphthalene oxidation over 1% Pt/γ-Al₂O₃ catalysts are reported for the first time. A first-order reaction with respect to P_naphthalene was found, while the reaction order with respect to P_O2 decreased with increasing reaction temperatures. A Langmuir–Hinshelwood model was used to describe the observed kinetic behavior. Oxygen adsorption dominates at higher reaction temperatures (>140 °C), and consequently the oxidation of naphthalene over the Pt catalysts appeared to be insensitive to P_O2.     

Selectively fluorinated analogs reveal differential olfactory reception and inactivation of green leaf volatiles in insects

The role of the alkyl terminus of green leaf volatile (GLV) molecules in olfactory reception and inactivation was examined in three diverse insect species: the beet armyworm,Spodoptera exigua (Lepidoptera); the Colorado potato beetle,Leptinotarsa decemlineata (Coleoptera); and the desert locust,Schistocerca gregaria (Orthoptera), using selectively fluorinated analogs of GLVs and electroantennograms (EAGs). When only the magnitude of the depolarization of the EAG is considered (a measure of reception), the order of effectiveness was 1-hexanol (6:OH)=(Z)-3-6:OH > 5,5,6,6,6-pentafluoro-(Z)-3-6:OH =5,5-difluoro-(Z)-3-6:OH 5,5,6,6,6-pentafluoro-6: OH. Percent recovery of the EAG (a measure of inactivation) was greater for the pentafluoro-(Z)-3-6: OH analog than for the difluoro-(Z)-3-6: OH analog. Our results show that the alkyl end of GLV molecules plays an important role not only in reception, but also inactivation processes in insect olfaction. Furthermore, specificities of these two processes may differ.Research conducted by J.C.D. while on an ARS Fellowship at IPO-DLO.     

A molybdenum dithiolene complex as a potential photosensitiser for photoelectrochemical cells

Molybdenum dithiolene complexes with the general formula [MoTp*(NO)(L)], where Tp* = tris(3,5-dimethylpyrazolyl)hydroborate and L = toluene-3,4-dithiolate (L1), 1,2-benzenedithiolate (L2), or 3,6-dichloro-1,2-benzenedithiolate (L3), were found to exhibit the chemical and physical properties required for a photosensitiser in a photoelectrochemical cell. These complexes were characterised using micro-elemental, spectroscopic (IR and UV–vis) and electrochemical analyses. Cyclic voltammetry (CV) was used to determine the oxidation/reduction potentials and to calculate the energy band gap. All of the complexes had an energy band gap in the range 1.45–1.48 eV, which extends far into the visible light region. A TiO₂ thin film to be used as a photoanode for photoelectrochemical cells was prepared using the paste technique on a Fluorine-doped Tin Oxide (FTO) plate and characterised using scanning electron microscope (SEM) and X-ray diffractometer (XRD). The [MoTp*(NO)(L)]-doped TiO₂ photoanodes were analysed photochemically in a 1.0 M NaOH electrolyte solution using SCE reference and platinum counterelectrodes. The [MoTp*(NO)(L3)]-doped TiO₂ photoanode exhibited an increased photoinduced current compared with the undoped TiO₂ photoanode. The Cl atoms on the dithiolene group offered a better interaction between the photosensitiser molecule and the TiO₂ photocatalyst by providing a means for halogen atom-induced chemical bonding. Based on the band edge calculations and the subsequent photocurrent results, these complexes may be potential photosensitisers for use in the preparation of photoelectrodes for photoelectrochemical cells.     

Temperature and rate dependent debonding behaviors of precision glass molding interface

The glass-to-mold adhesion in precision glass molding could severely degrade the quality of molded optics and shorten the lifespan of the precious molds. Since the consequences of adhesion take effect during the separation between glass and molds, it is important to investigate the debonding behaviors of a typical glass molding interface. To this end, here we perform a probe tack test procedure for borosilicate glass BK7, where debonding is conducted at molding temperature and specific velocity. We fully characterize the debonding behaviors using the peak adhesion stress σ_max and the work of debonding W_deb. Experiments show that when temperature is decreased from 690°C to 655°C at 10 μm/s, σ_max continuously increases, while W_deb first increases but then sharply decreases. When the debonding velocity is increased from 10 to 50 μm/s at 680°C, σ_max also increases while W_deb overall decreases. Therefore, the debonding behaviors are highly temperature and rate dependent. More importantly, depending on the debonding conditions, three debonding types are identified, that is, the cohesive bulk deformation, the cohesive-interfacial transition and the interfacial fracture. The cohesive type can be converted into the interfacial fracture, by either decreasing temperature or increasing the debonding velocity. Based on the W_deb criterion, the three debonding regimes can be clearly distinguished. Finally, analyses on the temperature and velocity experimental results are unified by incorporating the reduced crack velocity a_Tv_c. The dependences of both viscoelasticity and W_deb on a_Tv_c qualitatively explain the transition condition for different debonding types. Concerning these findings, the work of debonding not only supplements the characterization of adhesion strength, but also throws insightful light on revealing the debonding mechanisms.     

Effects of partial hydrogenation, epoxidation, and hydroxylation on the fuel properties of fatty acid methyl esters

The properties of biodiesel depend on the chemical structure of individual fatty acid methyl esters (FAME). In this work the chemical structure of fatty acid chains was modified by catalytic hydrogenation, epoxidation and hydroxylation under controlled conditions. Hydrolysis of ester functionality or oxidation of fatty acid chain was not observed during these reactions. The properties of hydrogenated FAME strongly depend on the hydrogenation time. The total saturated fatty acid (SFA) percentage increased from 29.3% to 76.2% after 2 h of hydrogenation. This hydrogenated FAME showed higher oxidation stability and higher cetane number but poor cold flow properties. Formation of trans FAME was observed during hydrogenation. Both hydroxylation and epoxidation resulted in a decrease of unsaturated fatty acid methyl ester (UFA) fraction. The percentages of total unsaturated FAME decreased 39% in the epoxidation reaction and 44% in the hydroxylation reaction. The addition of hydroxyl groups to the unsaturated regions of the fatty acid chain yields biodiesel with better cold flow properties, increased lubricity and slightly increased oxidative stability. However, epoxy FAME shows some interesting properties such as higher oxidation stability, higher cetane number and acceptable cold flow properties, which met the limits of ASTM D6751 biodiesel specifications.     

Coupled lateral-torsion vibration of asymmetric shear-wall structures

This paper presents an analysis of dynamic performance of asymmetric shear-wall structures. In the analysis, the asymmetric shear-wall structure is replaced by an equivalent thin-walled beam with lateral flexure and warping torsion deformations. Due to the asymmetry of the floor plan, the natural vibration of the structure is a coupled vibration, where lateral flexure vibrations in two orthogonal principal directions couple with a warping torsion vibration. Based on the continuum technique and the D'Alembert's principle, the governing differential equation of natural vibration and the corresponding eigenvalue problem for asymmetric multi-bent wall structures are derived. By employing the Galerkin technique, a method of solution is proposed for analysis of coupled vibration of generally asymmetric shear-wall structures and for estimate of the coupled natural frequencies and associated mode shape in coupled vibration. Results obtained from the proposed method for the example structure show good agreement with those of finite element analysis. It has been shown that the proposed analysis provides an efficient and accurate means of dynamic analysis of asymmetric shear-wall structures in coupled vibration.     

Investigation of assimilable organic carbon (AOC) and bacterial regrowth in drinking water distribution system

This paper investigated the variation of assimilable organic carbon (AOC) concentrations in water from several typical water treatment plants and distribution systems in a northern city of China. It is concluded from this study that: (1) The AOC in most of the product water of the studied water treatment plants and the water from the associated distribution systems could not meet the biostability criteria of 50-100 microg/L. (2) Only 4% of the measured AOC concentrations were less than 100 microg/L. However, about half of the measured AOC values were less than 200 microg/L. (3) Better source water quality resulted in lower AOC concentrations. (4) The variation of AOC concentrations in distribution systems was affected by chlorine oxidation and bacterial activity: the former resulted in an increase of AOC value while the latter led to a reduction in AOC. (5) The variation of AOC concentration followed different patterns in different distribution systems or different seasons due to their respective operational characteristics. (6) Less than 30% of AOC could be removed by a conventional treatment process, whereas 30-60% with a maximum of 50-60% could be removed by granular activated carbon (GAC). (7) The observation via scanning electron microscope (SEM) on distribution pipe tubercle samples demonstrated that the pipe inner wall was not smooth and bacteria multiplied in the crevice as well as in the interior wall of distribution pipes.