Hans Saveyn

Bio-deposition of a calcium carbonate layer on degraded limestone by Bacillus species

To obtain a restoring and protective calcite layer on degraded limestone, five different strains of the Bacillus sphaericus group and one strain of Bacillus lentus were tested for their ureolytic driven calcium carbonate precipitation. Although all the Bacillus strains were capable of depositing calcium carbonate, differences occurred in the amount of precipitated calcium carbonate on agar plate colonies. Seven parameters involved in the process were examined: calcite deposition on limestone cubes, pH increase, urea degrading capacity, extracellular polymeric substances (EPS)-production, biofilm formation, ζ-potential and deposition of dense crystal layers. The strain selection for optimal deposition of a dense CaCO3 layer on limestone, was based on decrease in water absorption rate by treated limestone. Not all of the bacterial strains were effective in the restoration of deteriorated Euville limestone. The best calcite precipitating strains were characterised by high ureolytic efficiency, homogeneous calcite deposition on limestone cubes and a very negative ζ-potential.

Accurate particle size distribution determination by nanoparticle tracking analysis based on 2-D Brownian dynamics simulation

A physical model is presented to simulate the average step length distribution during nanoparticle tracking analysis experiments as a function of the particle size distribution and the distribution of the number of steps within the tracks. Considering only tracks of at least five steps, numerical simulation could be replaced by a normal distribution approximation. Based on this model, simulation of a step length distribution allows obtaining a much more reliable estimation of the particle size distribution, thereby reducing the artificial broadening of the distribution, as is typically observed by direct conversion of step length to particle size data. As this fitting procedure also allowed including data from particles that were followed for a relatively low number of steps, the measurement time could be reduced for particles that are known to be monodisperse. Whereas the inversion is less sensitive towards the particle size distribution width, still similar values were obtained for both the average diameter and standard deviation of a polystyrene latex sample irrespective of the track length, provided that the latter included at least five steps.

Virus disinfection in water by biogenic silver immobilized in polyvinylidene fluoride membranes

The development of innovative water disinfection strategies is of utmost importance to prevent outbreaks of waterborne diseases related to poor treatment of (drinking) water. Recently, the association of silver nanoparticles with the bacterial cell surface of Lactobacillus fermentum (referred to as biogenic silver or bio-Ag(0)) has been reported to exhibit antiviral properties. The microscale bacterial carrier matrix serves as a scaffold for Ag(0) particles, preventing aggregation during encapsulation. In this study, bio-Ag(0) was immobilized in different microporous PVDF membranes using two different pre-treatments of bio-Ag(0) and the immersion-precipitation method. Inactivation of UZ1 bacteriophages using these membranes was successfully demonstrated and was most probably related to the slow release of Ag(+) from the membranes. At least a 3.4 log decrease of viruses was achieved by application of a membrane containing 2500 mg bio-Ag(0)(powder) m(-2) in a submerged plate membrane reactor operated at a flux of 3.1 L m(-2) h(-1). Upon startup, the silver concentration in the effluent initially increased to 271 μg L(-1) but after filtration of 31 L m(-2), the concentration approached the drinking water limit ( = 100 μg L(-1)). A virus decline of more than 3 log was achieved at a membrane flux of 75 L m(-2) h(-1), showing the potential of this membrane technology for water disinfection on small scale.

Microalgal bacterial floc properties are improved by a balanced inorganic/organic carbon ratio.

Microalgal bacterial floc (MaB‐floc) reactors have been suggested as a more sustainable secondary wastewater treatment. We investigated whether MaB‐flocs could be used as tertiary treatment. Tertiary influent has a high inorganic/organic carbon ratio, depending on the efficiency of the secondary treatment. In this study, the effect of this inorganic/organic carbon ratio on the MaB‐flocs performance was determined, using three sequencing batch photobioreactors. The MaB‐flocs were fed with synthetic wastewater containing 84, 42, and 0 mg L−1 C‐KHCO3 supplemented with 0, 42, 84 mg L−1 C‐sucrose, respectively, representing inorganic versus organic carbon. Bicarbonate significantly decreased the autotrophic index of the MaB‐flocs and resulted in poorly settling flocs. Moreover, sole bicarbonate addition led to a high pH of 9.5 and significant lower nitrogen removal efficiencies. Sucrose without bicarbonate resulted in good settling MaB‐flocs, high nitrogen removal efficiencies and neutral pH levels. Despite the lower chlorophyll a content of the biomass and the lower in situ oxygen concentration, 92–96% of the soluble COD‐sucrose was removed. This study shows that the inorganic/organic carbon ratio of the wastewater is of major importance and that organic carbon is requisite to guarantee a good performance of the MaB‐flocs for wastewater treatment. Biotechnol. Bioeng. 2011; 108:549–558.

Colloid–membrane interaction effects on flux decline during cross-flow ultrafiltration of colloidal silica on semi-ceramic membranes

In order to investigate colloid–colloid, as well as colloid–membrane interaction effects on the flux decline occurring during membrane processes, filtration tests were performed at different electrolyte concentrations, as well as at different pH values. The surface properties of the colloidal silica particles were determined by electrophoretic light scattering, whereas the surface charge characteristics of the ultrafiltration membranes were derived from streaming potential measurements. From the flux versus transmembrane pressure curves, it was derived that both high and low salt concentrations were preferable to optimise the permeate flux provided that both particles and membrane had similar charge characteristics. At low salt concentration, this behaviour was due to colloid–colloid as well as colloid–membrane repulsive interactions, which largely reduced concentration polarisation. At high salt concentrations, flocculation of the colloidal dispersions gave raise to large, porous flocs. As a consequence of the latter effect, the concentration–polarisation layer became highly permeable. On the other hand, a severe flux decline was observed at pH conditions where the colloidal particles and the ultrafiltration membrane were oppositely charged, giving rise to attractive electrostatic interactions. The results indicate that the performance of ultrafiltration membranes is strongly affected by its interaction with the colloidal particles in the feed. Optimum conditions are obtained if repulsive interactions prevail, which may be accomplished by proper conditioning of the feed.

Relevance of Two-Dimensional Brownian Motion Dynamics in Applying Nanoparticle Tracking Analysis

Nanoparticle Tracking Analysis (NTA) is an image analysis-based technique that deduces the particle size from the changing position of scattering diffusing particles in a sequence of images. It is shown that a basic understanding of the underlying physical principles largely helps to prevent artifacts. In fact, an inappropriate selection of both software parameters, such as maximum particle jump or minimum track length, as well as sample preparation aspects (such as degree of dilution) may give rise to inaccurate or even erroneous results.

A methodological approach for direct quantification of the activated sludge floc size distribution by using different techniques

The activated sludge floc size distribution (FSD) is investigated by using different measurement techniques in order to gain insight in FSD assessment as well as to detect the strengths and limitations of each technique. A second objective was to determine the experimental conditions that allow a representative and accurate measurement of activated sludge floc size distributions. Laser diffraction, Time Of Transition (TOT) and Dynamic Image Analysis (DIA) devices were connected in series. The sample dilution liquid, the dilution factor and hydraulic flow conditions avoiding flocculation proved to be important. All methods had certain advantages and limitations. The MastersizerS has a broader dynamic size range and provides accurate results at high concentrations. However, it suffers from an imprecise evaluation of small size flocs and is susceptible to particle shape effects. TOT suffers less from size overestimation for non-spherical particles. However, care should be taken with the settings of the transparency check. Being primarily a counting technique, DIA suffers from a limited size detection range but is an excellent technique for process visualization. All evaluated techniques turned out to be reliable methods to quantify the floc size distribution. Selection of a certain method depends on the purpose of the measurement.

Quantification of hydrolytic charge loss of DMAEA-Q-based polyelectrolytes by proton NMR spectroscopy and implications for colloid titration

Copolymers of acrylamide and quaternised dimethylaminoethyl acrylate (DMAEA-Q) constitute an economically important range of cationic polyelectrolytes used in sludge conditioning. The latter treatment involves charge neutralisation and bridging induced by these polymers. Since both of these phenomena rely on charge-driven sorption onto the negatively charged colloidal particles, the accurate assessment of their charge density is of primary importance in polyelectrolyte characterisation. The experimental determination of this characteristic generally relies on colloidal charge titration, in which the cationic polymer is titrated against an anionic polymer. Hereby, one of the requirements to have a stoichiometric reaction between the oppositely charged polymers is a sufficiently low polymer concentration. In this study, it is shown that such a low polymer concentration may entail a pronounced hydrolysis effect for DMAEA-Q-based polymers, which leads to a release of the cationic side groups and hence causes considerable errors on the charge titration results. Proton nuclear magnetic resonance spectroscopy was applied to investigate the fast hydrolysis kinetics of DMAEA-Q polymers together with time-dependent charge titration measurements. Diffusion NMR spectroscopy was used to assist in establishing the nature of the hydrolysis compounds. The results from both techniques indicate that a high degree of hydrolysis is reached within minutes after dilution of a concentrated polymer stock solution into aqueous solutions of slightly acidic to neutral pH values. Therefore, a modification to the classic colloid titration procedure is proposed, using a buffered dilution liquid to avoid polymer hydrolysis. It is shown that a buffer pH value of 4.5 avoids not only polymer hydrolysis effects but also possible protonation of the anionic titrant, thereby avoiding overestimation of the charge density. By means of this procedure, reproducible and time-independent charge titration results are obtained.

Determination of charge density and adsorption behaviour of DMAEA-Q-based cationic polymers by fluorimetric analysis

In wastewater and sludge treatment, cationic polymers are applied at large scale. A correct determination of the charge density and adsorption efficiency is of high importance for an economic and ecologically sound operation. Although several analytical techniques exist for charge density and polymer concentration determination, they often suffer from laborious sample pretreatment, complex instrumentation or interference from background components present in sludge. In this work, an alternative method has been studied to determine the charge density of an important series of cationic polymers used in water and sludge treatment, viz. copolymers containing quaternised dimethylaminoethylacrylate (DMAEA-Q). The method is based on the basic hydrolysis of the cationic moiety, resulting in choline chloride, which is measured by a fluorimetric technique based on the enzymatic conversion of choline. It was demonstrated that the new technique ensures a highly reliable determination of the charge density of these polymers, based on a comparison with the traditional charge titration technique and the data supplied by the manufacturer. Moreover, the specificity of the enzymatic conversion method also allows the determination of non-adsorbed polymer in conditioned sludge samples, without interference from other components. As a consequence, it enables the determination of the optimal polymer dose in practical conditioning and dewatering operations.

A method for visualising polyelectrolyte distribution after polyelectrolyte conditioning of a biotic sludge.

Charge neutralisation is an important mechanism in (polyelectrolyte) conditioning of biotic sludges and required for efficient sludge dewatering. Based on results from streaming potential and zeta potential measurements, it has been suggested that charge neutralisation is more complete on the outside of the sludge flocs than on the inside. This paper discusses the development of a technique for assessing the spatial distribution of polyelectrolyte (PE) within sludge flocs. After flocculation with a fluorescently labelled PE, fluorescence microscopy can be used to visualise the distribution of the PE in the sludge flocs. Preliminary results indicate that the PE can penetrate relatively deep into the sludge flocs (and flocculi). Inhomogeneity in the PE distribution arises from differences in exposure to PE in different regions, and from differences in the affinity of the PE for different substances.