Synthesis and characterization of CdS quantum dots with carboxylic-functionalized poly (vinyl alcohol) for bioconjugation

In the present research it is reported the synthesis and characterization of CdS nanoparticles (NPs) prepared using carboxylic-functionalized poly (vinyl alcohol) (PVA) as the ligand via aqueous route at room temperature and ambient pressure. Different molar concentrations of carboxylic-PVA and PVA were investigated aiming at producing stable colloidal systems. Carboxylic-PVA was conjugated with BSA (bovine serum albumin) and used as capping ligand in the preparation of CdS nanocrystals. UV-visible spectroscopy, photoluminescence spectroscopy, and transmission electron microscopy were used to characterize the kinetics and the relative stability of polymer-capped CdS nanocrystals. The results have clearly indicated that the carboxylic-functionalized PVA was much more effective on nucleating and stabilizing colloidal CdS nanoparticles in aqueous suspensions compared to PVA. In addition, the CdS nanocrystals were obtained in the so-called “quantum-size confinement regime”, with the calculated average size below 4.0 nm and fluorescent activity. Thus, a novel simple route was successfully developed for synthesizing nanohybrids based on quantum dots and water-soluble chemically functionalized polymers with incorporated carboxylic moiety with the possibility of direct bioconjugation.     

Evaluation of Coupling Agents in Poly(propylene)/Fly Ash Composites: Effect on Processing and Mechanical Properties

Composites containing 50 wt.‐% fly ash in a PP homopolymer were prepared via batch mixing and compression moulding. The following coupling agents were evaluated: Lubrizol Solplus C800, N,N′‐(1,3‐phenylene)dimaleimide, γ‐methacryloxypropyltrimethoxysilane and maleic‐anhydride‐grafted PP. At the filler level investigated, C800 gave the best balance of composite strength and toughness. In the latter case filler‐matrix adhesion appeared weaker relative to γ‐MPS, BMI and m‐PP, all of which gave excessively strong filler‐matrix adhesion leading to a reduction in composite toughness. The unexpected weakness of the C800/fly ash interaction may be related to removal of surface calcium ions from the fly ash via reaction of a single calcium ion with two C800 molecules.

     

Real‐time control of a semi‐industrial fed‐batch evaporative crystallizer using different direct optimization strategies

This article presents a model‐based control approach for optimal operation of a seeded fed‐batch evaporative crystallizer. Various direct optimization strategies, namely, single shooting, multiple shooting, and simultaneous strategies, are used to examine real‐time implementation of the control approach on a semi‐industrial crystallizer. The dynamic optimizer utilizes a nonlinear moment model for on‐line computation of the optimal operating policy. An extended Luenberger‐type observer is designed to enable closed‐loop implementation of the dynamic optimizer. In addition, the observer estimates the unmeasured process variable, namely, the solute concentration, which is essential for the intended control application. The model‐based control approach aims to maximize the batch productivity, as satisfying the product quality requirements. Optimal control of crystal growth rate is the key to fulfill this objective. This is due to the close relation of the crystal growth rate to product attributes and batch productivity. The experimental results suggest that real‐time application of the control approach leads to a substantial increase, i.e., up to 30%, in the batch productivity. The reproducibility of batch runs with respect to the product crystal size distribution is achieved by thorough seeding. The simulation and experimental results indicate that the direct optimization strategies perform similarly in terms of optimal process operation. However, the single shooting strategy is computationally more expensive. © 2010 American Institute of Chemical Engineers AIChE J, 57: 1557–1569, 2011     

Application of ultrasound for start‐up of evaporative batch crystallization of ammonium sulfate in a 75‐L crystallizer

A positive effect of ultrasound on crystallization has been shown for many applications especially on small scale. Predictable scale‐up of sonocrystallization is a challenge due to the inherent dependency of ultrasound on scale. The presented research discusses the experimental application of ultrasound to induce nucleation at low supersaturation for start‐up of evaporative batch‐wise crystallization of ammonium sulfate in a 75‐L draft tube (DT) crystallizer. A comparison is made with a conventional start‐up procedure using primary nucleation or seeding. Ultrasound is applied in two geometrically different vessels of 1.2‐L connected to a 75‐L DT crystallizer. Application of ultrasound for start‐up of a 75‐L DT crystallizer shows that an optimum amount of ground seeds is better capable to suppress nucleation. A challenge for future research is to improve the efficiency of ultrasound to produce a large number of nuclei for start‐up of batch crystallization at larger scale. © 2011 American Institute of Chemical Engineers AIChE J, 2011     

Molecular dynamics simulations as a tool for improving protein stability

Haloalkane dehalogenase (DhlA) was used as a model protein toexplore the possibility to use molecular dynamics (MD) simulationsas a tool to identify flexible regions in proteins that canserve as a target for stability enhancement by introductionof a disulfide bond. DhlA consists of two domains: an     

Preparation of spherical macroporous silica in an aerosol phase

Macroporous silica (MS) and macro/mesoporous silica (MMS) were prepared by spray drying a polystyrene (PS) latex sol containing a silica source, followed by calcination. As a silica source, 3-aminopropyl triethoxysilane (APS) was used for MS while either silica sol (SS) or tetraethoxyothosilicate using P123 templating (P123-TEOS) was used for MMS. Spray drying and calcination could also take place in a once-through aerosol reactor. The transformation of the silicon alkoxides to silica and decomposition of PS occurred at similar temperatures. Therefore, for APS-originated MS, the metal additives such as silver and nickel were required to accelerate the former. In addition, the nickel was well dispersed in the silica matrix during calcination even at 800 °C, in turn to thermally stabilize the porous structures. The wall-preforming additives were unnecessary for PS/SS and PS/P123-TEOS, since the SS drying and P123 templating, respectively, took place at lower temperature than PS decomposition. The porosities of all the porous silica prepared ranged from 0.54 to 0.57, which were close to the volume fraction of PS in the PS-alkoxides mixture solidified right after spray drying.     

Simulation study of the effect of wall roughness on the dynamics of granular flows in rotating semicylindrical chutes

A discrete element model (DEM) is used to investigate the behavior of spherical particles flowing down a semicylindrical rotating chute. The DEM simulations are validated by comparing with particle tracking velocimetry results of spherical glass particles flowing through a smooth semicylindrical chute at different rotation rates of the chute. The DEM model predictions agree well with experimental results of surface velocity and particle bed height evolution. The validated DEM model is used to investigate the influence of chute roughness on the flow behavior of monodisperse granular particles in rotating chutes. To emulate different base roughnesses, a rough base is constructed out of a square close packing of fixed spherical particles with a diameter equal to, smaller, or larger than the flowing particles. Finally, the DEM model is used to study segregation in a binary density mixture for different degrees of roughness of the chute. © 2015 American Institute of Chemical Engineers AIChE J, 61: 2117–2135, 2015     

Application of inline imaging for monitoring crystallization process in a continuous oscillatory baffled crystallizer

In this study, an in situ imaging system has been analysed to characterize the crystal size, the shape and the number of particles during a continuous crystallization process in a Continuous Oscillatory Baffled Crystallizer (COBC). Two image analysis approaches were examined for particle characterization in the suspension containing both small nuclei and larger grown crystals (nonspherical and irregular in shape). The pattern matching approach, in which the particles are approximated to be spherical, did result in an overestimation of the size. Alternatively, a segmentation‐based algorithm resulted in reliable crystal size and shape characteristics. The laser diffraction analysis in comparison to the image analysis overestimated the particle sizes due to the agglomeration of particles upon filtration and drying. The trend in the particle counts during the start of crystallization process, including nucleation, determined by the image analysis probe was comparable with the one measured by FBRM, highlighting the potential of in situ imaging for process monitoring. © 2018 American Institute of Chemical Engineers AIChE J, 64: 2450–2461, 2018     

Clean coal conversion options using Fischer-Tropsch technology

Material and energy balances were prepared for two coal conversion options for the co-production of liquid hydrocarbon products and electricity. The results are compared to the alternative approach of producing liquid hydrocarbons from natural gas. It is concluded that the capital cost for coal conversion must be higher but that cash operating costs may be similar. There are important synergistic effects so that facilities co-producing liquid hydrocarbons and electricity from coal are more efficient than facilities producing these products individually. There may be good strategic reasons to use clean coal conversion plants co-producing liquid hydrocarbons and electricity. Due to the huge capital investments required, some form of government assistance will be needed.     

Coordination‐Assisted Bioorthogonal Chemistry: Orthogonal Tetrazine Ligation with Vinylboronic Acid and a Strained Alkene

Bioorthogonal chemistry can be used for the selective modification of biomolecules without interfering with any other functionality that might be present. Recent developments in the field include orthogonal bioorthogonal reactions to modify multiple biomolecules simultaneously. During our research, we observed that the reaction rates for the bioorthogonal inverse‐electron‐demand Diels–Alder (iEDDA) reactions between nonstrained vinylboronic acids (VBAs) and dipyridyl‐s‐tetrazines were exceptionally higher than those between VBAs and tetrazines bearing a methyl or phenyl substituent. As VBAs are mild Lewis acids, we hypothesised that coordination of the pyridyl nitrogen atom to the boronic acid promoted tetrazine ligation. Herein, we explore the molecular basis and scope of VBA–tetrazine ligation in more detail and benefit from its unique reactivity in the simultaneous orthogonal tetrazine labelling of two proteins modified with VBA and norbornene, a widely used strained alkene. We further show that the two orthogonal iEDDA reactions can be performed in living cells by labelling the proteasome by using a nonselective probe equipped with a VBA and a subunit‐selective VBA bearing a norbornene moiety.