The
polymer gel systems are mostly used for the control of excessive
water production during enhanced oil recovery operations in mature
oil fields. However, these polymer gels are not stable in the high-temperature
and high-salinity reservoir. Keeping these in mind, an attempt was
made to investigate the effect of several parameters on the gelation
time of polymer gels for its suitable application in the oil fields.
In this paper, a polymer gel comprised of partially hydrolyzed polyacrylamide
as a water-soluble polymer and hydroquinone and hexamine as organic
cross-linking agents
of low toxicity was prepared to control excessive water production.
The effect of various parameters such as polymer and cross-linker
concentrations, temperature, pH, and salinity on the gelation time
and gel strength was evaluated using the bottle testing method, and
variations in the performance of the polymer system were analyzed
under different gel compositions and environmental conditions.
During appendicular skeletal development, the bi-potential cartilage anlagen gives rise to transient cartilage, which is eventually replaced by bone, and articular cartilage which caps the ends of individual skeletal elements. While the molecular mechanism that regulates transient cartilage differentiation is relatively better understood, the mechanism of articular cartilage differentiation has only begun to be unraveled. Further, the molecules that coordinate articular and transient cartilage differentiation processes are very poorly understood. Here, we have characterized the regulatory roles of two transcription factors, NFIA and GATA3 in articular cartilage differentiation, maintenance and the coordinated differentiation of articular and transient cartilage. Both NFIA and GATA3 block hypertrophic differentiation. Our results suggest that NFIA is not sufficient but necessary for articular cartilage differentiation. On the other hand, while ectopic activation of GATA3 promotes articular cartilage differentiation, inhibition of GATA3 activity promotes transient cartilage differentiation at the expense of articular cartilage. Finally, we propose a novel transcriptional circuitry involved in embryonic articular cartilage differentiation, maintenance and its cross-talk with transient cartilage differentiation program.
Removal of metals from wastewaters causes a big concern from the environmental point of view due to their extreme toxicity towards aquatic life and humans. Application of As(III) from aqueous solution by ZnO nanorods as adsorbent has been investigated in the present study. The synthesized nanorods were characterized by XRD, FT-IR spectroscopy, SEM, and thermogravimetric analysis. Optimum biosorption conditions were determined with respect to pH, adsorbent dose, contact time, and temperature. The experimental data were examined using the Lagergren's first-order, pseudo-second-order and intraparticle diffusion kinetic models. The results revealed that the pseudo-second-order kinetic model provided the best description of the data. Langmuir and Freundlich isotherm models were applied to the equilibrium data. The maximum As(III) sorption capacity of ZnO nanorods was found to be 52.63 mg/g at pH 7, adsorbent dose 0.4 g, contact time 105 min, and temperature 323 K. The calculated thermodynamic parameters, ΔG o (between − 5.741, − 5.342 and − 4.538 kJ/mol at 303-323 K), ∆H o (13.75 kJ/mol) and ∆S o (0.0616 J/mol K) showed that the sorption of As(III) onto ZnO nanorods was feasible, spontaneous and exothermic, respectively.
Limb skeleton forms through the process of endochondral ossification. This process of osteogenesis proceeds through an intermediate cartilage template and involves several stages of chondrocyte maturation and eventual bone formation. During the process of endochondral ossification, interplay between BMP and WNT signaling regulate simultaneous differentiation of articular and transient cartilage. In this review, we focus on the recent literature which explores the simultaneous differentiation of these two different types of cartilage. We discuss a new paradigm of developmental biology-inspired tissue engineering of bone and cartilage grafts and provide novel insight into treatment of osteoporosis.
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