Co‐composting an animal fatty‐proteinaceous waste with a solid lignocellulosic by‐product from the olive oil industry (‘alperujo’)

BACKGROUND: The production of biodegradable wastes and their disposal cause a major financial problem in many industrial activities. Co‐composting was thought to be a feasible alternative for disposing of a strongly alkaline waste from the pharmaceutical industry (AW), mainly consisting of animal fats and partially hydrolysed proteins in a stable emulsion. The AW was added gradually, during the early phase of the composting process, to a substrate made up of ‘alperujo’ (AL), the wet, lignocellulosic, solid by‐product of the olive oil industry, and fresh horse manure, which was added to improve the physical structure of the composting substrate. RESULTS: The addition of AW reduced organic matter degradation during composting, enriched the amount of organic compounds in the water‐ and alkali‐soluble fractions and increased mineral salt contents. Thus, significantly higher electrical conductivity, humification indices and contents of organic matter, P, K and Na were recorded in the end‐composts resulting from AW treatments. However, the application of one AW‐based compost led to soil N immobilisation, as revealed by an incubation experiment, which must be considered in order to avoid potential N starvation in the short term. CONCLUSION: According to these results, composting can be used as a disposal alternative for AW, leading to end‐products with potential uses as organic amendments or fertilisers for agricultural systems. In addition, these composts could be used to produce alternative liquid organic fertilisers, based on the extraction of their humic‐like fraction. Copyright © 2009 Society of Chemical Industry     

3D reconstruction of SOFC anodes using a focused ion beam lift-out technique

Improvements to electrode performance are essential to accelerate the commercialisation of SOFC technology. A key metric of performance for SOFC electrodes is the length and distribution of three or triple phase boundaries (TPBs) which provide an indication of electrochemical performance. Techniques that can be used to characterise TPB length are highly valuable; with an increasing knowledge of electrode microstructures, electrochemical performance can be optimised. One such technique for electrode characterisation uses focused ion beams (FIB) to sequentially mill and image an electrode surface, obtaining a sequence of 2D images that may be reconstructed in a 3D space. In this paper we present a technique to maximise the quality of the raw data obtained via ex-situ characterisation of electrode micro-sections based on FIB lift-out. With improved raw data, we have been able to conduct semi-automated image analysis to extract key microstructural information, including the length and distribution of TPBs.Reconstructions have been carried out using both single and dual beam instruments; two reconstructions of Ni-YSZ anode structures are presented here.     

Kinetic investigation of C38 steel corrosion in concentrated perchloric acid solutions

The corrosion behaviour of steel at various concentrations of perchloric acid was studied by weight loss method in temperature range from 298 to 323 K. Results obtained show that corrosiveness of acid increases with its concentration and temperature. The logarithm of corrosion rate was plotted against the acid concentration and values of Hammett H_o and Strehlow R_o(H) acidity functions. The activation energies, enthalpies and entropies of the corrosion process of steel were also determined and fitted against R_o(H).     

Textile injection process characterisation by means of a spiral mould

New developments are being carried out within the injection moulding field, such as gas injection, bi-injection, co-injection, sequential injection, compression injection or textile injection processes. These techniques require new developments as they highly modify design and process conditions. In this work, the influence over the plastic material flow of the introduction of different film textiles into the mould is measured. A specific measurement system consisting of a monitorised spiral mould with pressure sensors has been used to measure the influence of different tissues over the mould pressures. As an application of this measurement system, a viscous model is generated to characterise the rheological behaviour of the thermoplastic and textile joint. The viscous model obtained is applied on a conventional CAE tool for the simulation of textile injection pressure results for the different film textiles analysed.     

Delamination failures of Stellite hardfacing in power plants: a microstructural characterisation study

In recent years, several incidents of cracking and failures have been observed in Stellite (Stellite is a registered trademark of the Deloro-Stellite Corporation) hardfacing used in valves of modern high temperature combined cycle gas fired power plants. These hardfacing layers are applied as an overlay onto a steel substrate, such as CrMo steel (i.e. Grade 22, WC9) or creep strength enhanced ferritic steel (i.e. Grade 91, C12A). Cracking has been observed in valve components at the Stellite/steel interface and in the weld dilution zone formed between the steel and clad. Ultimately, disbonding or delamination of the weld hardfacing from the valve body occurs and has resulted in collateral damage to components in the plant (such as to the turbine) or valve failure. In this study, the microstructure formed near the Stellite/steel interface is investigated. Based on thermodynamic modelling, microstructure formed at these regions is hypothesised and a simple methodology is proposed to predict the occurrence of these failures.     

Synthesis of zeolite beta using silica gel as a source of SiO2

The feasibility of synthesising pure zeolite beta in high yields using silica gel as the source of SiO₂ is demonstrated. The phase-purity and yield of beta is enhanced by using silica gels with high surface area. The influence of various synthesis parameters (Si/Al ratio, alkalinity, dilution level, concentration of the organic base, etc.) on the kinetics of synthesis as well as the quality and yield of the zeolite have been investigated. A correlation between XRD crystallinity of the samples with varying degrees of crystallinity and that estimated from framework IR spectroscopy, differential thermal analysis and adsorption of n-hexane is demonstrated. The dependence of the yield of zeolite beta on SiO₂/Al₂O₃ ratio of the gel is also reported. The results of the present study indicate the feasibility of a cheaper route for the manufacture of zeolite beta.     

A novel methodology in transforming bulk properties of refining streams into molecular information

Stricter and ever increasing environmental legislations and demand for higher quality products are the driving forces for the refiner in an attempt to characterise the refining streams on the molecular basis. The objective of this work is to develop a new methodology to interrelate the bulk properties and molecular information of the refining streams in order for refiners to look at the contribution of each molecular group on the properties of the refining streams.The molecular information of a particular refining stream is presented in the form of MTHS (molecular type homologous series) matrix representation [Peng, B., 1999. Molecular modelling of petroleum processes. Ph.D. Thesis, UMIST]. To enhance the accuracy and usability of the method, structural contribution of each isomer on various properties such as octane number, and reid vapour pressure, etc. are considered. Structural lumping rules are then applied to obtain the physical properties of each homologous series. Databases are set up for the properties and molecular information of typical refining streams. Automatic selection of sample matrices through linear combination is used to predict new composition matrices. The methodology is illustrated for refining streams with gasoline range hydrocarbons. The properties predicted based on the new methodology proves to be within 5-6% error range.     

Permeability of low molecular weight organics through nanofiltration membranes

The removal of natural organic matter (NOM) using nanofiltration (NF) is increasingly becoming an option for drinking water treatment. Low molecular weight (LMW) organic compounds are nevertheless only partially retained by such membranes. Bacterial regrowth and biofilm formation in the drinking water distribution system is favoured by the presence of such compounds, which in this context are considered as the assimilable organic carbon (AOC). In this study, the question of whether NF produces microbiologically stable water was addressed. Two NF membranes (cut-off of about 300 Da) were tested with different natural and synthetic water samples in a cross-flow filtration unit. NOM was characterised by liquid chromatography with organic carbon detection (LC-OCD) using a size-exclusion column in addition to specific organic acid measurements, while AOC was measured in a batch growth bioassay.Similarly to high molecular weight organic compounds like polysaccharides or humic substances that have a permeability lower than 1%, charged LMW organic compounds were efficiently retained by the NF membranes tested and showed a permeability lower than 3%. However, LMW neutrals and hydrophobic organic compounds permeate to a higher extent through the membranes and have a permeability of up to 6% and 12%, respectively. Furthermore, AOC was poorly retained by NF and the apparent AOC concentration measured in the permeated water was above the proposed limit for microbiologically stable water. This indicates that the drinking water produced by NF might be biologically unstable in the distribution system. Nevertheless, in comparison with the raw water, NF significantly reduced the AOC concentration.     

Characterisation of proteolytic enzymes from muscle and hepatopancreas of fresh water prawn (Macrobrachium rosenbergii)

BACKGROUND: Fresh water prawn in Thailand is widely consumed due to its delicacy. During postmortem handling and storage, prawn meat becomes soft and mushy, probably as a result of indigenous proteases. Therefore, an understanding of prawn proteases associated with the degradation of muscle proteins from fresh water prawn could pave the way for prevention of such a phenomenon during extended storage. RESULTS: Proteolytic enzymes in the crude extract (CE) from muscle and hepatopancreas of fresh water prawn (Macrobrachium rosenbergii) were characterised. CE from muscle exhibited the highest hydrolytic activities towards haemoglobin at pH 5 and 50 °C, while that from hepatopancreas had the highest activity on casein at pH 7 and 60 °C. Based on inhibitor study, cysteine protease and serine protease were dominant in CE from muscle and hepatopancreas, respectively. CE from muscle rarely hydrolysed natural actomyosin (NAM), but could not degrade pepsin‐soluble collagen (PSC). Conversely, NAM and PSC were susceptible to hydrolysis by CE from hepatopancreas as evidenced by the marked decreases in band intensity. Activity staining using haemoglobin, casein and gelatin as substrates revealed that no proteolytic or gelatinolytic activity was observed in CE from prawn muscle, while CE from hepatopancreas exhibited pronounced hydrolytic activities towards all substrates. CE from muscle showed calpain and cathepsin L activities but CE from hepatopancreas mainly exhibited tryptic and chymotryptic activities. CONCLUSION: Serine proteases, mainly trypsin‐like or chymotrypsin‐like, from hepatopancreas were probably responsible for the softening of prawn meat during postmortem storage via the degradation of both muscle and connective tissues. Copyright © 2010 Society of Chemical Industry     

Polymeric compounds in activated sludge supernatant -- Characterisation and retention mechanisms at a full-scale municipal membrane bioreactor

In this study, for the first time a full-scale membrane bioreactor (MBR) was investigated with focus on organic compounds in activated sludge over a period of approximately 2 years. Soluble extracellular polymeric substances (EPS) in the sludge supernatant and permeate as well as bound EPS extracted from fouled membranes were determined photospectrometrically and revealed a typical composition of three main components in the order metals>humic acids>carbohydrates>proteins. Results showed an important influence on membrane fouling by soluble humic substances and carbohydrates in complexes with metal cations. It was found that Fe(2+) and Fe(3+) play a decisive role in natural organic matter (NOM) complexation and subsequent membrane blockage. The determination of molar mass distribution in supernatant and permeate by size exclusion chromatography (SEC) revealed a significant retention of macromolecular compounds by the porous membranes in the range of 10-50%.