Impact of salts on polyacrylamide hydrolysis and gelation: New insights

Polyacrylamide (PAM) and its derivatives are the most commonly used polymers in the preparation of polymeric gels for water control in petroleum reservoirs. This study involved the use of polyethylenimine (PEI) as a crosslinker for PAM. In this study, we investigated PAM alkaline hydrolysis at high temperatures. The effects of salts [sodium chloride (NaCl) and ammonium chloride (NH₄Cl)] on the degree of hydrolysis (DH) of PAM were investigated. These salts were used as retarders to elongate the gelation time of the PAM/PEI system. The data obtained from ¹³C‐NMR was used to understand the retardation mechanisms by salts. We found that NH₄Cl accelerated the extent of hydrolysis more in comparison with NaCl. Moreover, the apparent viscosity of the hydrolyzed samples was measured. PAM hydrolysis in the presence of NH₄Cl resulted in a lower solution viscosity than that in the presence of NaCl. Therefore, NH₄Cl was more effective in shielding negative charges on the carboxylate groups of the partially hydrolyzed polyacrylamide (PHPA) chain. NaCl and NH₄Cl were compatible with the PHPA/PEI system, but sodium carbonate showed a white precipitate. In addition, high‐temperature/high‐pressure elastic modulus data were reported for the first time for this system. Differential scanning calorimetry was coupled with rheology to explain the PAM/PEI crosslinking in the presence of salts. Models were developed to assess the impact of the salts on the PAM DH and the induction period before gelation. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41185.     

Recent Advances in Reactions of Alkylbenzenes Over Novel Zeolites: The Effects of Zeolite Structure and Morphology

Alkylbenzenes form an important segment of petrochemical industry for the manufacture of widely used commodities and specialty products. Since the last review on this topic (8), numerous new zeolite-based catalysts have been synthesized, characterized and evaluated in various transformations of aromatic hydrocarbons. This comprehensive review covers major reactions of mono-, di-, and tri-alkylbenzenes such as disproportionation, alkylation, transalkylation, isomerization, etc., over different zeolite-based acid catalysts. During the last decade, significant progress was made in the synthesis and structure determination of novel zeolites, mesoporous single crystals, hierarchic zeolites and two-dimensional zeolites. These developments have enhanced the understanding of the role of zeolites (effects of structural type, morphology, acid sites, accessibility of acid sites, shape selectivity factors) in transformations of aromatics. In this review, the emphasis is on the influence of the type of acid sites, zeolite topology, and reaction conditions on the activity, selectivity and pathways of these reactions. Thermodynamics and reaction kinetics of transformations of aromatic hydrocarbons are also discussed. This article covers mostly literature published during the period of 2002–2013.     

Synthesis of Dy2O3 nanoparticles via hydroxide precipitation： effect of calcination temperature

This work described the preparation of dysprosium oxide, Dy2O3, nanoparticles using the homogeneous precipitation method. Dy3+ ions were precipitated using NaOH solution. The obtained product was filtered, dried, and then calcined for 1 h at the temperature range of 300–700 °C in static air. The calcination temperature of the Dy-precursor was chosen based on its decomposition as indicated by the TGA analysis. The crystalline structure and surface morphology of the calcined solids were studied by X-ray diffraction(XRD), field emission scanning electron microscopy(FE-SEM), transmission electron microscopy(TEM) and X-ray photoelectron spectroscopy(XPS). The obtained results revealed that Dy2O3 with crystallites size of 11–21 nm was formed at 500 °C. Such value increased to 25–37 nm for the sample calcined at 700 °C.     

Polyvinylidene fluoride and polyetherimide hollow fiber membranes for CO2 stripping in membrane contactor

Porous polyvinylidene fluoride (PVDF) and polyetherimide (PEI) hollow fiber membranes incorporating polyethylene glycol (PEG) were prepared via spinning process for CO₂ membrane stripping. CO₂ loaded diethanolamine solution was used as liquid absorbent while N₂ was used as a strip gas. The characterization study of the fibers was carried out in terms of permeation test, contact angle measurement and liquid entry pressure (wetting pressure). Performance study via membrane contactor stripping was carried out at specific operating condition. The experimental results showed that PVDF membrane have high gas permeation, effective surface porosity and contact angle despite having lower liquid entry pressure in comparison with PEI membrane. PVDF-PEG membrane showed the highest stripping flux of 4.0 × 10⁻² mol m⁻² s⁻¹ at 0.7 ms⁻¹ compared to that of PEI membrane. Although the stripping flux for PEI-PEG membranes was slightly lower than PVDF membrane (e.g. 3.5 × 10⁻² mol m⁻² s⁻¹ at liquid velocity of 0.85 ms⁻¹), the membrane wetting pressure of PEI membrane is higher than hydrophobic PVDF membrane. Long term performance of both membranes showed severe flux reduction but started to level-off after 30 h of operation.     

CFD and experimental investigation of the gas–liquid flow in the distributor of a compact heat exchanger

High performance of compact heat exchangers is conditioned by correct fluid distribution. This is especially true for gas–liquid heat exchangers where a uniform distribution is particularly delicate to obtain and where maldistribution entails significant performance deterioration. Several phenomena can lead to phase distribution problems: the fins may be subject to manufacturing defects or fouling, leading to shortcuts or dead zones. But the first source of maldistribution may be a poor distribution at the outlet of the entrance distributor. This distributor aims at mixing the phases and distributing them across the channels.     

Boosting the performance of visible light‐driven WO3/g‐C3N4 anchored with BiVO4 nanoparticles for photocatalytic hydrogen evolution

In this article, a ternary WO₃/g‐C₃N₄@ BiVO₄ composites were prepared using eco‐friendly hydrothermal method to produce efficient hydrogen energy through water in the presence of sacrificial agents. The prepared samples were characterized by scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), transmission electron microscopy (TEM), X‐ray diffraction (XRD), ultraviolet‐visible (UV‐vis), Brunauer‐Emmett‐Teller (BET) surface area, and photoluminescence spectroscopy (PL) emission spectroscopy. The experimental study envisages the formation of 2‐D nanostructures and observed that such kinds of nanostructures could provide more active sites for photocatalytic reduction of water and their inherent reactive‐species mechanism. The results showed the excellent photocatalytic performance (432 μmol h^?1 g^?1) for 1.5% BiVO₄ nanoparticles in WO₃/g‐C₃N₄ composite when compared with pure WO₃ and BiVO₄. The optical properties and photocatalytic activity measurement confirmed that BiVO₄ nanoparticles in WO₃/g‐C₃N₄ photocatalyst inhibited the recombination of photogenerated electron and holes and enhanced the reduction reactions for H₂ production. The enhanced photocatalytic efficiency of the composite nanostructures may be attributed to wide absorption region of visible light, large surface area, and efficient separation of electrons/holes pairs owing to synergistic effects between BiVO₄ and WO₃/g‐C₃N₄. The prepared samples would be a precise optimal photocatalyst to increase their suppliers for worldwide applications especially in energy harvesting.     

Facile synthesis of cobalt-doped (Zn,Ni)(O,S) as an efficient photocatalyst for hydrogen production

Cobalt-doped (Zn,Ni)(O,S) or Co-(Zn,Ni)(O,S) was facilely synthesized at low temperature below 100 °C with different cobalt precursor contents for photocatalytic hydrogen production. The X-ray pattern and elemental mapping proved that cobalt was successfully doped into zinc sites in the (Zn,Ni)(O,S) host lattice. We found the incorporation with a small amount of cobalt into (ZnNi)(O,S) enhanced its photo activity for hydrogen production. The best hydrogen production was achieved for 2.5% Co-(ZnNi)(O,S) with a rate of 8,527 μmol/g·h during a span of 5 h in a 20% (v/v) ethanol/water solution. Based on the results of optical characterizations, the enhancement of hydrogen production was caused by the slow electron-hole recombination and the low charge transfer resistance. A different photocatalytic kinetic mechanism for hydrogen generation from the conventional one with the simultaneous formation of hydrogen and oxygen gases is proposed, based upon the activated surface oxygen anion to initiate or trigger the key reaction of oxidation for water splitting to proceed. Our strategy in preparing catalyst at low process temperature and in doping to activate catalyst is for weakening the lattice oxygen bonding on the catalyst surface in order to firstly initiate the oxidation reaction and the formation of oxygen vacancies. These freshly formed oxygen vacancies play a critical role to trap the water and weaken its OH bonding to form hydrogen gas through the reduction reaction.