Relocation Counselling and Supportive Services as Tools to Prevent Negative Spillover Effects: A Review

This paper aims to review the literature on negative neighbourhood spillovers connected to four voluntary housing mobility programs: Gautreaux 1 and Gautreaux 2 (Chicago), the Moving to Opportunity Fair Housing Demonstration (five cities) and the Baltimore Housing Mobility Program. Although these four programs involve voluntary moves, a great deal may be learned from them because of (1) efforts to forestall community opposition and (2) special counselling and supportive programs provided to ease adjustment into destination neighbourhoods. Unfortunately, the available research often falls short in providing evidence for or against negative spillover effects. Nevertheless, our review indicates that screening out multi-problem families, limiting the number of housing voucher families moving into particular neighbourhoods and providing both pre- and post-relocation counselling to program participants can minimize the risk of negative neighbourhood spillovers.     

Identification of 11,15-octadecadienoic acid from beef and mutton tallow

By means of gas liquid chromatography and thin layer chromatography on Silica gel G/AgNO₃ we isolated some isolinoleic acids from beef and mutton tallow, which by their chromatographical behavior, IR analysis and by double bond determination by ozonolysis are mainly stereo-isomeric 11,15-octadecadienoic acids and in a smaller amount stereo-isomers of 10,15-octadecadienoic acids. 4-Cis- and 4-trans-heptenals, 2-trans,6-cis- and 2-trans,6-trans-nonadienals have been isolated from the DNPH mixture obtained from the volatile decomposition products of an oxidized synthetic mixture of stereo-isomeric 11,15-octadecadienoic acids. Presented in part by G. Hoffmann at the 7th ISF Congress, Hamburg, October 1964.     

Catalyst Deactivation Rate During Hydrogenation of CO2 to Longer-Chained Hydrocarbons Over 6 wt% Potassium-Promoted Co/Al2O3 Catalyst

Catalysis Letters - The deactivation rate of 15%Co-6%K/Al2O3 Fischer–Tropsch catalyst during hydrogenation of CO2 to longer-chained hydrocarbons was investigated. The catalysts used were...     

LCA of second generation bioethanol: A review and some issues to be resolved for good LCA practice

This paper aims at reviewing the life cycle assessment (LCA) literature on second generation bioethanol based on lignocellulosic biomass and at identifying issues to be resolved for good LCA practice. Reviews are carried out on respective LCA studies published over the last six years. We use the classification of lignocellulosic biomass to define system boundaries, so that the comparison among LCA results can be thoroughly assessed based on identified system components. A basis for attributing environmental burden for different biomass feedstocks is also suggested. Despite the non-homogeneous systems, we conclude that second generation bioethanol performs better than fossil fuel at least for the two most studied impact categories, net energy output and global warming. For the latter category, carbon sequestration at the biomass generation stage can even consistently offset the GHG emissions from all parts of the life cycle chains at high ethanol percentage (≥85%). The aspect of biogenic carbon and agrochemical input for energy crops and biomass residues, and the effect of removal of the latter from soil have not been treated consistently. In contrast, the exclusion of upstream chain of biomass waste feedstocks is observed in practice. The bioethanol conversion process is mostly based on simultaneous saccharification and co-fermentation, characterized by high yield and low energy input. In this regard, the LCA results tend to under estimate the real impacts of the current technology. The choice of allocation methods strongly influences the final results, particularly when economic value is used as a reference. Substitution of avoided burden seems to be the most popular allocation method in practice, followed by partition based on mass, energy, and economic values.     

Are alcohol expectancies associations? Comment on Moss and Albery (2009).

Moss and Albery (see record 2009-09537-002) presented a dual-process model of the alcohol–behavior link, integrating alcohol expectancy and alcohol myopia theory. Their integrative theory rests on a number of assumptions including, first, that alcohol expectancies are associations that can be activated automatically by an alcohol-relevant context, and second, that alcohol selectively reduces propositional reasoning. As a result, behavior comes under the control of associative processes after alcohol consumption. We agree with the second but not with the first assumption, based on theoretical and empirical arguments. Although in some cases expectancies may involve a simple association, they are propositional in nature. We demonstrate that this assertion is supported by existing literature cited in Moss and Albery. Moreover, 6 recent studies consistently demonstrated that under circumstances in which executive control is impaired (either as a stable individual difference or under the acute influence of alcohol), associative processes, over and above expectancies, predict alcohol-related behavior. Taken together, the evidence strongly suggests a fundamental distinction between expectancies and associations in memory: Effects of propositional expectancies and executive functions are impaired under the acute influence of alcohol, but memory associations are not. This difference in perspective not only has theoretical implications but also leads to different predictions regarding acute alcohol effects in society. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Current and future trends of additive manufacturing for chemistry applications: a review

Three-dimensional (3-D) printing, also known as additive manufacturing, refers to a method used to generate a physical object by joining materials in a layer-by-layer process from a three-dimensional virtual model. 3-D printing technology has been traditionally employed in rapid prototyping, engineering, and industrial design. More recently, new applications continue to emerge; this is because of its exceptional advantage and flexibility over the traditional manufacturing process. Unlike other conventional manufacturing methods, which are fundamentally subtractive, 3-D printing is additive and, therefore, produces less waste. This review comprehensively summarises the application of additive manufacturing technologies in chemistry, chemical synthesis, and catalysis with particular attention to the production of general laboratory hardware, analytical facilities, reaction devices, and catalytically active substances. It also focuses on new and upcoming applications such as digital chemical synthesis, automation, and robotics in a synthetic environment. While discussing the contribution of this research area in the last decade, the current, future, and economic opportunities of additive manufacturing in chemical research and material development were fully covered.

Graphical abstract

     

pH-independent immediate release polymethacrylate formulations – an observational study

Abstract

Using Eudragit® E PO (EudrE) as a polymethacrylate carrier, the aim of the study was to develop a pH-independent dosage form containing ibuprofen (IBP) as an active compound via chemical modification of the polymer (i.e. quaternization of amine function) or via the addition of dicarboxylic acids (succinic, glutaric and adipic acid) to create a pH micro-environment during dissolution. Biconvex tablets (diameter: 10?mm; height: 5?mm) were produced via hot melt extrusion and injection molding. In vitro dissolution experiments revealed that a minimum of 25% of quaternization was sufficient to partially (up to pH 5) eliminate the pH-dependent effect of the EudrE/IBP formulation. The addition of dicarboxylic acids did not alter IBP release in a pH 1 and 3 medium as the dimethyl amino groups of EudrE are already fully protonated, while in a pH 5 solvent IBP release was significantly improved (cf. from 0% to 92% release after 1?h dissolution experiments upon the addition of 20?wt.% succinic acid). Hence, both approaches resulted in a pH-independent (up to pH 5) immediate release formulation. However, the presence of a positively charged polymer induced stability issues (recrystallization of API) and the formulations containing dicarboxylic acids were classified as mechanically unstable. Hence, further research is needed to obtain a pH-independent immediate release formulation while using EudrE as a polmethacrylate carrier.     

Preparation and physicochemical evaluation of a new tacrolimus tablet formulation for sublingual administration

The aim of this study was to develop a new fast-disintegrating tablet formulation containing 1?mg tacrolimus for sublingual application. First, solid dispersions containing tacrolimus (2.5%, 5% and 10% w/w) incorporated in Ac-Di-Sol(?) and carriers (inulin 1.8?kDa and 4?kDa, and polyvinylpyrrolidone (PVP) K30) were prepared by freeze drying. Subsequently, a tablet formulation composed of a mixture of the solid dispersions, Ac-Di-Sol(?), mannitol, Avicel(?) PH-101 and sodium stearyl fumarate was optimized concerning drug load in the solid dispersions and the type of carrier. Tablet weight was kept constant at 75?mg by adjusting the amount of Avicel(?) PH-101. Differential scanning calorimetry (DSC) and X-ray powder diffraction (XRPD) results indicated the absence of the drug in the crystalline state, which was confirmed by the scanning electron microscopy (SEM). These results suggest that tacrolimus incorporated in all of the solid dispersions was fully amorphous. Dissolution of the tablets containing solid dispersions with a low drug load highly depends on the type of carrier and increased in the order: PVP K30 < inulin 4?kDa < inulin 1.8?kDa. Solid dispersions with a drug load of 10% w/w incorporated in the carriers yielded optimal formulations. In addition, the physicochemical characteristics and the dissolution behavior of the tablet formulation containing inulin 1.8 kDa-based solid dispersions with a drug load of 10% w/w did not change after storage at 20°C/45%RH for 6 months indicating excellent storage stability.