Does living in a poor neighbourhood result in network poverty? A study on local networks,locality-based relationships and neighbourhood settings

This paper examines whether and how living in a poor neighbourhood results in “network poverty”. Through a detailed analysis of the formation of personal networks of people living in a poor neighbourhood and those living in an affluent neighbourhood in Rotterdam, I examine the role of the neighbourhood in the formation of personal networks. I address three issues. First, whether resource-poor people who live in a poor neighbourhood form relationships with fellow-residents to compensate for their otherwise small network. I find that they do not and that their small network is primarily caused by non-participation in settings such as study, work, leisure and associations. Second, I distinguish locally maintained relationships that have originated in other settings from locality-based relationships that originated in the neighbourhood. The study shows that high network localness is more a matter of maintaining relationships in the neighbourhood than forming many new locality-based relationships with fellow-residents. Third, I examine how the neighbourhood facilitates relationship formation and conclude that this happens not in “the neighbourhood” but in neighbourhood settings, which attract a particular segment of a neighbourhood population. I conclude that the problem of network poverty is not in the first place spatial but rather lies in lack of participation in certain settings. Furthermore, social mixing policies can only be successful if they are accompanied by initiatives to draw a mixed population to neighbourhood settings and facilitate routine encounters between resource-rich and resource-poor people.     

Fluidization behavior in a circulating slugging fluidized bed reactor. Part I: Residence time and residence time distribution of polyethylene solids

Square nosed slugging fluidization behavior in a circulating fluidized bed riser using a polyethylene powder with a very wide particle size distribution was studied. In square nosed slugging fluidization the extent of mixing of particles of different size depends on the riser diameter, gas velocity, hold up and solids flux in the riser. Depending on the operating conditions the particle residence time distribution of a riser in the slugging fluidization regime can vary from that of a plug flow reactor to that of a well-mixed system.Higher gas velocities cause shorter particle residence times because of a significant decrease in the hold-up of particles in the riser at higher gas velocities. A higher solids flux also shortens the average residence time. Both influences have been quantified for a given polyethylene-air system.Residence time and residence time distribution were determined for different particle size and the influence of gas velocity, solids flux, hold up and riser diameter was studied. When comparing data from segregation and residence time experiments it is clear that segregation data can predict the spread in residence time as a function of overall residence time, particle size and gas velocity. The differential velocity between small and large particles found in the segregation experiments can predict the spread in residence time as found in the residence time distribution experiments with a powder with a broad particle size distribution. Raining of particles through the slugs was studied as a function of plug length, gas velocity and pulse length. It was found that raining is not the determining mechanism for segregation of particles.     

The Sites of Molecular and Dissociative Hydrogen Adsorption in High-Silica Zeolites Modified with Zinc Ions. III DRIFT Study of H2 Adsorption by the Zeolites with Different Zinc Content and Si/Al Ratios in the Framework

study of dihydrogen adsorbed at 77K by the zinc-modified hydrogen forms of mordenite and ZSM-5 zeolites with the different Si/Al ratios in the framework indicated the existence of several adsorption sites connected with the modifying zinc ions. The fraction of the sites of the strongest perturbation of adsorbed molecular hydrogen with the H–H stretching frequency of ca. 3930–3950 cm^-1 is the highest at the highest Si/Al ratios of 41 or 80. These sites dissociatively adsorb hydrogen at moderately elevated temperatures. Adsorption of hydrogen with the higher H–H stretching frequency of about 3970–4000 cm^-1 predominates at the lower Si/Al ratios. It does not result in the dissociation of adsorbed molecules. It was concluded that the most active sites are most probably connected with the zinc ions, which compensate two distantly separated negatively charged [AlO₄]^- tetrahedra localized in the adjacent five- or six-membered rings on the walls of the large channels of the pentasil's framework. The sites of the weaker perturbation of adsorbed hydrogen are most probably connected with Zn⁺² ions at the conventional exchangeable cationic positions with two aluminum atoms in the same five- or six-membered ring.     

CO2 binding capacity of alkali-activated fly ash and slag pastes

Quantification of the CO₂ binding capacity of reinforced concrete is of high importance for predicting the carbonation potential and service life of concrete structures. Such information is still not available for alkali activated materials that have received extensive attention as a sustainable substitute for ordinary Portland cement (OPC)-based concrete. To address this gap, this paper evaluates the CO₂ binding capacity of ground powders of alkali activated fly ash (FA) and ground granulated blast furnace slag (GBFS) pastes under accelerated carbonation conditions (1% v/v CO₂, 60% RH, 20?°C) for up to 180 days. The CO₂ binding capacity, the gel phase changes, and the carbonate phases are investigated with complementary TG-DTG-MS, FT-IR and QXRD techniques.Five mixtures with different FA/GBFS ratio are considered. CEM I and CEM III/B pastes are also studied to provide a baseline for comparisons. The results showed that the alkali-activated pastes have a lower CO₂ binding capacity in comparison to cement-based pastes. Furthermore, alkali-activated pastes have similar CO₂ binding capacity regardless of the FA/GBFS ratio. It was observed that the silicate functional groups corresponding to the reaction products in the pastes were progressively changing during the first 7 days, after which only carbonate groups changed. It was also found that the CO₂ bound in the alkali-activated pastes occurs to a substantial extent in amorphous form.

Functionalizable composite nanoparticles as a dual magnetic resonance imaging/computed tomography contrast agent for medical imaging

A dual contrast agent for computed tomography (CT) and magnetic resonance imaging (MRI) was synthesized via microemulsion polymerization. This contrast agent consists of Fe₃O₄ particles (d = 7 nm) with an iodine-carrying nanopolymeric shell, with overall particle sizes ranging from 50 to 250 nm. 2-Methacryloyloxyethyl(2,3,5-triiodobenzoate) was used as the monomer. Sodium oleate was used as the surfactant and its amount was varied to control the overall particle size. The composite nanoparticles were mainly characterized via dynamic light scattering, with further analyses using transmission electron microscopy and atomic force microscopy. The particles provided a highly visible contrast in CT and MR images. A template for biomedical applications was created by adding a comonomer and the particles were further functionalized with the somatostatin analogue Tyr³-octreotate. The particles were tested for specific uptake into somatostatin receptor-positive AR42J cells. The additional uptake of the functionalized particles was investigated. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47571.     

Comparison of ras-p21 bound to GDP and GTP: differences in protein and ligand dynamics

This paper documents the first essential dynamics analysis of ras protein ligands and of the protein itself, showing important features of their dynamic properties. Essential dynamics analysis of 300 ps of full solvent molecular dynamics simulations revealed differences in structure and dynamics between GDP- and GTP-bound forms of H-ras-p21. Regions in the protein which exhibited a structural shift correspond to the switch regions described previously. Differences in dynamics between H-ras-p21 GDP and H-ras-p21 GTP may be related to interactions of ras with GAP and its receptor and effector. Molecular dynamics of free GDP (in the absence of protein) were performed in water for 2 ns and analysed using essential dynamics. The conformations of GDP and GTP when bound to the protein were compared with free GDP, revealing that the ligands bind to the protein in an energetically unfavourable conformation. GDP and GTP molecules from various other protein crystal structures were also analysed. These ligands adopt similar conformations to those seen in H-ras-p21.      

Pore functioning of outer membrane protein PhoE of Escherichia coli: mutagenesis of the constriction loop L3

Each monomer of the trimeric outer membrane porin PhoE of Escherichia coli consists of a 16-stranded beta-barrel with short turns at the periplasmic side and large loops at the cell surface. One of these loops, L3, is folded inside the beta-barrel and forms a constriction within the channel. Therefore, it is assumed to play an important role in the permeability properties of this general diffusion pore. Several site-directed mutations were introduced in loop L3 to investigate its function. The loop L3 contains a short alpha-helix and, at the tip of the loop, a highly conserved PEFGG sequence. The alpha-helix was deleted and the two glycines in the PEFGG sequence were either replaced by alanines or deleted. A serine residue, supposed to play an indirect role in the anion selectivity of the pore, was removed. The mutant porins were analysed both in vitro and in vivo. The results suggest that flexibility of the third loop is important for solute passage and that this flexibility is determined by the two glycine residues in the PEFGG sequence. Furthermore, the alpha-helix is probably important for the folding of the protein. The supposed involvement of Ser115 (Ser121A in OmpF nomenclature) in anion selectivity was confirmed.      

Upgrading the AOCS infrared trans method for analysis of neat fats and oils by fourier transform infrared spectroscopy

An automated protocol for the direct, rapid determination of isolated trans content of neat fats and oils by Fourier transform infrared (FTIR) spectroscopy was devised, based on a simple modification of the standard AOCS trans method, eliminating the use of CS₂ and methylation of low trans samples. Through the use of a commercially available, heated transmission flow cell, designed specifically for the analysis of neat fats and oils, a calibration (0–50%) was devised with trielaidin spiked into a certified, trans-free soybean oil. The single-beam spectra of the calibration standards were ratioed against the single-beam spectrum of the base oil, eliminating the spectral interference caused by underlying triglyceride absorptions, facilitating direct peak height measurements as per the AOCS IR trans method. The spectrometer was preprogrammed in Visual Basic to carry out all spectral manipulations, measurements, and calculations to produce trans results directly as well as to provide the operator with a simple interface to work from. The derived calibration was incorporated into the software package, obviating the need for further calibration because the program includes an automatic recalibration/standardization routine that automatically compensates for differences in optical characteristics between instruments, instrument drift over time, and cell wear. The modified AOCS FTIR analytical package was evaluated with Smalley check samples for repeatability, reproducibility, and accuracy, producing SD of ± 0.07, 0.13, and 0.70 trans, respectively, the FTIR predictions being linearly related to the Smalley means (r=0.999; SD=± 0.46), and well within one SD of the Smalley sample means. Calibration transfer was assessed by implementing the calibration on a second instrument and reanalyzing the Smalley check samples in cells of two different pathlengths (25- and 50-μm). There were no statistically significant differences between the FTIR trans predictions obtained for the Smalley samples from the two instruments and two cells, indicating that the software was able to adjust the calibrations to compensate for differences in instrument response and cell pathlength. The FTIR isolated trans analysis protocol developed by the McGill IR Group has the benefit of being based on the principles of an AOCS-approved method, matches its accuracy, and allows the analysis to be performed on both neat fats and oils, producing trans predictions in less than 2 min per sample. It is suggested that this integrated approach to trans analysis, which requires a minimum level of sample manipulation and operator skill, be considered as a modification of the proposed Recommended Practice CD14b-95.     

A quantum-chemical study of hydride transfer in catalytic transformations of paraffins on zeolites. Pathways through adsorbed nonclassical carbonium ions

A quantum-chemical investigation of the hydride transfer reaction in catalytic transformations of hydrocarbons on zeolites has been performed. Ab initio calculations at the MP2/6-31++G^**//HF/6-31G^* level demonstrated that the activated complexes of hydride transfer reaction in catalytic transformations of paraffins on zeolites very much resemble adsorbed nonclassical carbonium ions. However, these transient species are strongly held at the surface active sites by the Coulomb interaction. The calculated activation energies for reactions involving propane and isobutane are in a reasonable agreement with the experimental data. This revised version was published online in July 2006 with corrections to the Cover Date.     

Powder coatings technology: new developments at the turn of the century

The growth of the powder coating business is affected by the toxicological effects of the raw materials used in the coating formulation and the saturation of the present market for powder coatings, being limited to general metal applications only. This has a strong influence on the long-term research programmes at both raw materials suppliers and powder paint producers. In the last decade of the 20th century, we witness appearance of several new types of toxicologically-safe powder coating systems on the commercial scale. At the same time, there is strong evidence of efforts to penetrate new market fields where powder coatings are not typically used. This includes the markets for automotive clear top coatings, can and coil coatings, coatings for industrial wood, plastics and paper. The new developments in the chemistry of powder coatings are followed by changes and improvements in the production technology for powder coatings as well as developments of new application techniques. This paper summarises the research work on chemistry, production and application technology of powder coatings and tries to extrapolate the tendencies in the years to come in order to predict the achievements and the impacts on the paint industry.