Aluminium Foil as a Food Packaging Material in Comparison with Other Materials

Aluminium foil is an important material in laminates and has wide application in food packaging. Its barrier function against the migration of moisture, oxygen and other gases, and volatile aroma, as well as against the impact of light is generally higher than any plastic laminate material. Therefore, aluminium foil is used in the laminates when insufficient barrier properties are the limiting factor for shelf-life stability of food. The barrier properties of aluminium-coated plastic laminates, which can offer an alternative to aluminium foil laminates, are somewhat less efficient. The use of aluminium foil in rigid, semirigid, and flexible package for in-pack thermal processing allows the selection of package geometries that ensure rapid heating and minimum heat damage during processing. On the tightness of packages, the mechanical stability and quality of sealing is of particular importance. The chemical stability of aluminium foil in contact with food depends on the composition of the food items. With present toxicological knowledge, the use of aluminium in packaging material is considered to be safe, and inner-coating of the foil is recommended in specific cases.     

Carbon Dioxide Evolution and Moisture Evaporation During Roasting of Coffee Beans

ABSTRACT: Evolution of carbon dioxide and water vapor during roasting of coffee was followed in an isothermal high-temperature short-time and a low-temperature long-time roasting process. In addition, CO₂ release during storage of roasted beans was followed. CO₂ and water vapor concentration were assayed in the exhaust air by nondispersive infrared gas analysis. Although CO₂ evolution rates differed in the 2 processes, the final total amount of CO₂ released after 63 d of storage remained equal. CO₂ evolution and differentiation between evaporation of initial water and chemically formed water showed that chemical reactions leading to relevant amounts of CO₂ and water start at ap -proximately 180°C. A mass balance established on the present measurements was able to account fairly well for the gravimetrically measured roast loss.     

Modell eines Roboters aus Formgedächtnismetall

Zusammenfassung Im Fahmen diese Beitrags wird des Modell eines Roboters vorgestellt, der seine Bewegung ohne jegliche elektromotorische oder pneumatische Antriebe aufsührt. Entsprechende Bauelemente sind übedflüszig, da der Werkstoff, aus dem der Raboter gefertigt ist, die Greiffunktion selbst durchführt. Dies geschieht über das Signal einer Temperatur?nderung, so da? die Bauteile lediglich erw?rmt oder abgekühll werden müssen, um die Greifbewegung zu realisieren. Diese Eigenschaft von Werkstoffen nennt man ?Formged?chtnis?: Der Werkstoff erinnert sich bei Temperatur?nderungen an seine vorherige Form und nimmt diese selbst?ndig an. Es handelt sich dabei, um eine v?llig neue Werkstoffeigenschaft, nicht um eine lediglich verbesserte. Der Formged?chtniseffekt ist hinsichtlich seiner Ursachen sehr komplex und neu, so da? zum besseren Verst?ndnis die Grundlagen des Effektes vertieft in diesem Bericht beschrieben werden.     

Rosemary Extract and Precooking Effects on Lipid Oxidation in Heat-Sterilized Meat

The influence of precooking and addition of refined rosemary extract on lipid oxidation during storage of heat-sterilized meat in trays was investigated. Short precooking resulted in increased lipid oxidation, while more extended precooking using peanut oil gave products with higher stability during storage. The addition of a gravy-type sauce (instead of water) to the meat when filling it into trays also resulted in higher storage stability. However, only the application of rosemary extract, especially after precooking, resulted in products with stability similar to those packed with nitrogen flushing.     

Capacities of membrane lipids to accumulate neutral organic chemicals

Lipids have been considered as the predominant components for bioaccumulation of organic chemicals. However, differences in accumulation properties between different types of lipid (e.g., storage and membrane lipids) have rarely been considered. Moreover, in view of toxic effects on organisms, chemical accumulation specifically in biological membranes is of particular importance. In this review article, partition coefficients of 240 neutral organic compounds between liposomes (phospholipid membrane vesicles) and water (K(lipw)), reported in the literature or measured additionally for this work, were evaluated. Values of log K(lipw) and log K(ow) (octanol-water partition coefficients) differ by 0.4 on average. Polyparameter linear free energy relationships (PP-LFERs) can describe the log K(lipw) data even better (standard deviations = 0.28-0.31) than the log K(ow) model. Recent experimental data for highly hydrophobic compounds fit well to the PP-LFERs and do not indicate the existence of a previously postulated "hydrophobicity cutoff". Predictive approaches based only on the molecular structure (KOWWIN, SPARC, COSMOthermX, COSMOmic) were also evaluated for K(lipw) prediction. The PP-LFERs revealed that partition coefficients into membrane lipids can be two log units higher than those into storage lipids for H-bond donor compounds, suggesting that distinguishing between the two lipids is necessary to account for the bioaccumulation of these compounds, and that tissues rich in membrane lipids (e.g., kidneys, liver) instead of fat tissue can be the primary phase for accumulation.     

Recent advances in environmental risk assessment of transformation products

When micropollutants degrade in the environment, they may form persistent and toxic transformation products, which should be accounted for in the environmental risk assessment of the parent compounds. Transformation products have become a topic of interest not only with regard to their formation in the environment, but also during advanced water treatment processes, where disinfection byproducts can form from benign precursors. In addition, environmental risk assessment of human and veterinary pharmaceuticals requires inclusion of human metabolites as most pharmaceuticals are not excreted into wastewater in their original form, but are extensively metabolized. All three areas have developed their independent approaches to assess the risk associated with transformation product formation including hazard identification, exposure assessment, hazard assessment including dose-response characterization, and risk characterization. This review provides an overview and defines a link among those areas, emphasizing commonalities and encouraging a common approach. We distinguish among approaches to assess transformation products of individual pollutants that are undergoing a particular transformation process, e.g., biotransformation or (photo)oxidation, and approaches with the goal of prioritizing transformation products in terms of their contribution to environmental risk. We classify existing approaches for transformation product assessment in degradation studies as exposure- or effect-driven. In the exposure-driven approach, transformation products are identified and quantified by chemical analysis followed by effect assessment. In the effect-driven approach, a reaction mixture undergoes toxicity testing. If the decrease in toxicity parallels the decrease of parent compound concentration, the transformation products are considered to be irrelevant, and only when toxicity increases or the decrease is not proportional to the parent compound concentration are the TPs identified. For prioritization of transformation products in terms of their contribution to overall environmental risk, we integrate existing research into a coherent model-based, risk-driven framework. In the proposed framework, read-across from data of the parent compound to the transformation products is emphasized, but limitations to this approach are also discussed. Most prominently, we demonstrate how effect data for parent compounds can be used in combination with analysis of toxicophore structures and bioconcentration potential to facilitate transformation product effect assessment.     

A screening level fate model of organic contaminants from advanced water treatment in a potable water supply reservoir

Augmentation of potable water sources by planned indirect potable reuse of wastewater is being widely considered to address growing water shortages. Environmental buffers such as lakes and dams may act as one of a series of barriers to potable water contamination stemming from micropollutants in wastewater. In South-East Queensland, Australia, current government policy is to begin indirect potable reuse of water from reverse osmosis equipped advanced water treatment plants (AWTPs) when the combined capacity of its major storages is at 40% capacity. A total of 15 organic contaminants including NDMA and bisphenol A have been publically reported as detected in recycled water from one of South-East Queensland’s AWTPs, while another 98 chemicals were analysed for, but found to be below their detection limit. To assess the natural attenuation in Lake Wivenhoe, a Level III fugacity based evaluative fate model was constructed using the maximum concentrations of these contaminants detected as input data. A parallel aquivalence based model was constructed for those contaminants, such as dichloroacetic acid, dalapon and triclopyr, which are ionised in the environment of Lake Wivenhoe. A total of 247 organic chemicals of interest, including disinfection by-products, pesticides, pharmaceuticals and personal care products, xenoestrogens and industrial chemicals, were evaluated with the model to assess their potential for natural attenuation. Out of the 15 detected chemicals, trihalomethanes are expected to volatilise with concentrations in the outflow from the dam approximately 400 times lower than influent from the AWTPs. Transformation processes in water are likely to be more significant for NDMA and pharmaceuticals such as salicylic acid and paracetamol as well as for caffeine and the herbicides dalapon and triclopyr. For hydrophobic contaminants such as cholesterol and phenolic xenoestrogens such as 4-nonylphenol, 4-t-octylphenol and bisphenol A, equilibrium between water and sediments will not be attained and hence fate processes such as removal in outflow are predicted to become relatively important.     

Natural versus wastewater derived dissolved organic carbon: implications for the environmental fate of organic micropollutants

The interaction of organic micropollutants with dissolved organic carbon (DOC) can influence their transport, degradation and bioavailability. While this has been well established for natural organic carbon, very little is known regarding the influence of DOC on the fate of micropollutants during wastewater treatment and water recycling. Dissolved organic carbon-water partition coefficients (K_DOC) for wastewater derived and reference DOC were measured for a range of micropollutants using a depletion method with polydimethylsiloxane disks. For micropollutants with an octanol-water partition coefficient (log K_OW) greater than 4 there was a significant difference in K_DOC between reference and wastewater derived DOC, with partitioning to wastewater derived DOC over 1000 times lower for the most hydrophobic micropollutants. The interaction of nonylphenol with wastewater derived DOC from different stages of a wastewater and advanced water treatment train was studied, but little difference in K_DOC was observed. Organic carbon characterisation revealed that reference and wastewater derived DOC had very different properties due to their different origins. Consequently, the reduced sorption capacity of wastewater derived DOC may be related to their microbial origin which led to reduced aromaticity and lower molecular weight. This study suggests that for hydrophobic micropollutants (log K_OW > 4) a higher concentration of freely dissolved and thus bioavailable micropollutants is expected in the presence of wastewater derived DOC than predicted using K_DOC values quantified using reference DOC. The implication is that naturally derived DOC may not be an appropriate surrogate for wastewater derived DOC as a matrix for assessing the fate of micropollutants in engineered systems.     

Some thoughts on the aquarius program: A prospective world effort in hydrogen-energy

Increasing discussion of what actions the US, and the world community generally, can take in the sphere of energy is being heard. The tempo is picking up; mention of 'lscrash programme’ possibilities is even made. Now may be the time to bring forward focused ideas, especially those which may make long-term sense. One such idea is that of a ‘hydrogen-energy system’ about which much has been written and spoken, but little yet accomplished in the sense of physical development.The United States is well known for its ability to establish an effective large-scale programme, once the stage of ‘determination’ has been reached, usually late-in-the-day in the sense of our facing up to the basic problem. This paper sketches out a ‘program-matistion’ of the hydrogen-energy concept somewhat in the spirit of the Apollo Program with which there are some parallels. But ‘Aquarius’ would be a much more ambitious and longer termed programme. It would involve practically all US citizens and, hopefully, gain international participation. Expensive? Of course. But the monies spent are with the identical constituency who would profit from the transition from fossil fuels.