High Mass Recovery Research Articles

Phosphorus recycling from waste activated sludge using the hydrothermal platform: Recovery, solubility and phytoavailability

To address the grand challenge of increasing the sustainability of wastewater treatment plants, hydrothermal carbonization was studied as a nutrient recovery platform, transforming sludge into a valuable hydrochar. Carbonization was achieved at different temperatures (200–300 °C) and durations (30–120 min). The highest mass recovery (73%) was observed in the lowest temperature, while the lowest (49%) was obsereved at the highest temperature. Under all reaction conditions, phosphorus recovery values exceeded 80%, with the dominated fraction of inorganic-P in the hydrochar being HCl-extractable. Although HCl-extractable P is considered a moderately labile P fraction, P phytoavailability assays indicate that sewage sludge hydrochar is an excellent source for P, surpassing soluble P, likely due to its slow-release nature. We postulate that polyphosphates constitute a significant portion of this P pool. Overall, we emphasize the benefits of using HTC as a circular economy approach to convert sludge into a valuable hydrochar.

Transport of nanoscale zero-valent iron in saturated porous media: Effects of grain size, surface metal oxides, and sulfidation

Knowledge of the fate and transport of nanoscale zero-valent iron (nZVI) in saturated porous media is crucial to the development of in situ remediation technologies. This work systematically compared the retention and transport of carboxymethyl cellulose (CMC) modified nZVI (CMC-nZVI) and sulfidated nZVI (CMC-S-nZVI) particles in saturated columns packed with quartz sand of various grain sizes and different surface metal oxide coatings. Grain size reduction had an inhibitory effect on the transport of CMC-S-nZVI and CMC-nZVI due to increasing immobile zone deposition and straining in the columns. Metal oxide coatings had minor effect on the transport of CMC-S-nZVI and CMC-nZVI because the sand surface was coated by the free CMC in the suspensions, reducing the electrostatic attraction between the nZVI and surface metal oxides. CMC-S-nZVI displayed greater breakthrough (C/C0 = 0.82–0.90) and higher mass recovery (84.9%–89.3%) than CMC-nZVI (C/C0 = 0.70–0.80 and mass recovery = 70.9%–79.6%, respectively) under the same experimental conditions. A mathematical model based on the advection-dispersion equation simulated the experimental data of nZVI breakthrough curves very well. Findings of this study suggest sulfidation could enhance the transport of CMC-nZVI in saturated porous media with grain and surface heterogeneities, promoting its application in situ remediation.

Groundwater flow numerical model to evaluate the water mass balance and flow patterns in Groundwater Circulation Wells (GCW) with varying aquifer parameters

Groundwater Circulation Wells (GCW) can be an effective in-situ remediation option allowing high mass recovery of contaminants in cases where contamination hotspots are located in saturated soil having low hydraulic conductivity. Traditional treatment options such as Pump&Treat, Air Sparging (AS)/Soil Vapor Extraction (SVE) and Multi Phase Extraction (MPE) typically require long operation times and significant costs for long-term plume management. GCWs induce meaningful changes in the groundwater flow introducing vertical flows both downward and upward, generating a “circulation cell”, which facilitates contaminant desorption from the soil. This study aims to understand the effects of a GCW on an aquifer in terms of both groundwater flow directions and water balance. A groundwater numerical model was built using MODFLOW-2005 to simulate the effect of the hydraulic parameters of the aquifer on the hydraulic circulation pattern of the GCW. The use of particle tracking simulated by MODPATH 7 showed the circulation cells and the impact on groundwater directions induced by different configurations of hydraulic parameters. The water flowing into the cell comes from both the injection well and the surrounding aquifer and the model shows how the hydraulic parameters of the aquifer, in particular the horizontal and vertical hydraulic conductivity, have a paramount influence in determining the shape and dimension of the circulation cell. A water mass balance analysis was carried out. It allowed to predict the groundwater flows exchanges between the GCW system and the surrounding aquifer, and to verify the sensitivity of the water budget to specific aquifer parameters. The results of this study are useful for further understanding the hydraulics of a GCW remediation system in order to support the design and to predict its performance.

Transport of marine tracer phage particles in soil

Marine phages have been applied to trace ground- and surface water flows. Yet, information on their transport in soil and related particle intactness is limited. Here we compared the breakthrough of two lytic marine tracer phages (Pseudoalteromonas phages PSA-HM1 and PSA-HS2) with the commonly used Escherichia virus T4 in soil- and sand-filled laboratory percolation columns. All three phages showed high mass recoveries in the effluents and a higher transport velocity than non-reactive tracer Br−. Comparison of effluent gene copy numbers (CN) to physically-determined phage particle counts or infectious phage counts showed that PSA-HM1 and PSA-HS2 retained high phage particle intactness (Ip > 81%), in contrast to T4 (Ip < 36%). Our data suggest that marine phages may be applied in soil to mimic the transport of (bio-) colloids or anthropogenic nanoparticles of similar traits. Quantitative PCR (qPCR) thereby allows for highly sensitive quantification and thus for the detection of even highly diluted marine tracer phages in environmental samples.

Estimating mean molecular weight, carbon number, and OM∕OC with mid-infrared spectroscopy in organic particulate matter samples from a monitoring network

Abstract. Organic matter (OM) is a major constituent of fine particulate matter, which contributes significantly to degradation of visibility and radiative forcing, and causes adverse health effects. However, due to its sheer compositional complexity, OM is difficult to characterize in its entirety. Mid-infrared spectroscopy has previously proven useful in the study of OM by providing extensive information about functional group composition with high mass recovery. Herein, we introduce a new method for obtaining additional characteristics such as mean carbon number and molecular weight of these complex organic mixtures using the aliphatic C−H absorbance profile in the mid-infrared spectrum. We apply this technique to spectra acquired non-destructively from Teflon filters used for fine particulate matter quantification at selected sites of the Inter-agency Monitoring of PROtected Visual Environments (IMPROVE) network. Since carbon number and molecular weight are important characteristics used by recent conceptual models to describe evolution in OM composition, this technique can provide semi-quantitative, observational constraints of these variables at the scale of the network. For this task, multivariate statistical models are trained on calibration spectra prepared from atmospherically relevant laboratory standards and are applied to ambient samples. Then, the physical basis linking the absorbance profile of this relatively narrow region in the mid-infrared spectrum to the molecular structure is investigated using a classification approach. The multivariate statistical models predict mean carbon number and molecular weight that are consistent with previous values of organic-mass-to-organic-carbon (OM/OC) ratios estimated for the network using different approaches. The results are also consistent with temporal and spatial variations in these quantities associated with aging processes and different source classes (anthropogenic, biogenic, and burning sources). For instance, the statistical models estimate higher mean carbon number for urban samples and smaller, more fragmented molecules for samples in which substantial aging is anticipated.

Field-scale investigation of nanoscale zero-valent iron (NZVI) injection parameters for enhanced delivery of NZVI particles to groundwater

The effects of the injection parameters on delivery of nanoscale zero-valent iron (NZVI) to contaminated groundwater were investigated. The first two NZVI injections (gravity injection at low flow rates) resulted in NZVI being poorly mobile and gave total cumulative mass recoveries at the monitoring wells of 1.07%–2.43%. NZVI reached some wells (KDMW-3, MW-2, MW-4, and MW-7) earlier than the bromide tracer. The dominant travel directions for NZVI and the bromide tracer were very different. The NZVI transport characteristics suggested that targeted NZVI delivery requires preferential groundwater flow paths and local heterogeneity to be considered. In the gravity injection tests, the maximum NZVI concentrations and cumulative NZVI mass recoveries in the wells decreased markedly as the injected NZVI concentration and dose increased. In the third and fourth tests, in which NZVI was injected under pressure at high flow rates, NZVI was effectively delivered to the wells despite the injected NZVI concentration and dose being high. Relatively high cumulative mass recoveries of 26.0% and 74.5% were found for the third and fourth injections, respectively. Controlling the flow rate (pressure) and NZVI concentration and dose simply and effectively controlled NZVI mobility in the groundwater. The colloidal and electrostatic characteristics of the NZVI particles were monitored and modeled, and the results indicated that NZVI particles without Derjaguin–Landau–Verwey–Overbeek energy barriers were successfully delivered to the target zone and that decreased magnetic attractive forces between NZVI particles caused by iron corrosion probably decreased the degree of NZVI particle aggregation and therefore contributed to NZVI being delivered to the target zone.

Silver Recovery from Silver Fluoride Solution Using Electrowinning

As solar technology becomes more popular, more modules with limited lifetimes will be manufactured. By 2050 there are expected to be 78 million tons of waste modules, which are rarely recycled today. Each module contains approximately 6 grams of silver, which is the most precious metal found in silicon modules. Hydrofluoric acid is proposed as the leaching agent to remove silver and other metals from the surface of the silicon, while electrowinning is used to recover the silver from the leachate and plate it onto a cathode. The electrowinning setup uses a three-electrode configuration with a pseudo reference electrode to control the half-cell potential. A silver pseudo-reference electrode was found to be sufficient for achieving a high mass recovery rate. Variable voltage trials were conducted and 0.7 V with reference to silver achieved a high mass recovery rate of 96.4% with a high purity of silver. Current efficiency is below 7% for all the voltages tested, which suggests parasitic reactions in the reaction vessel such as O2(g) + 4H+ + 4e− ⇌ 2H2O. The trials at 0.7 V vs silver in a nitrogen purge environment eliminated corrosion at the vapor-liquid interface on the cathode but did not improve the current efficiency. It is possible that the nitrogen purge environment still contains residual oxygen.

New amino group functionalized porous carbon for strong chelation ability towards toxic heavy metals.

Herein, ethylenediamine functionalized porous carbon (PC-ED/1.5) was synthesized, then characterized by various methods and finally used as a functional material for Cu(ii) and Pb(ii) ion removal from water. XPS revealed the presence of numerous functionalities within the surface of PC including –NH and C–N–C groups. Furthermore, SBET, RS, XRD and FTIR analyses confirmed the changes implemented on the PC surface. Thereafter, a systematic study was implemented to analyze the interactions of the PC-ED/1.5 surface with Cu(ii) and Pb(ii) heavy metal ions. Hence, adsorption experiments showed that the PC-ED/1.5 exhibits maximum adsorption capacities of 123.45 mg g−1 and 140.84 mg g−1 for Cu(ii) and Pb(ii), respectively. Moreover, in situ electrostatic interactions occurring between the divalent cation and the PC-ED/1.5 functional groups was investigated. The mechanism involves chelation processes, electrostatic interactions and mechanical trapping of the metal ions in the adsorbent pores. Interestingly, a synergistic effect of the pores and surface active sites was observed. Finally, by using alginate bio-polymer we prepared membrane films of PC-ED/1.5 which showed long-term stability, regeneration capabilities and high mass recovery.

The use of enrichment ratios to support kinetic studies in flotation

This paper presents the use and evaluation of enrichment ratios (ER) from different batch flotation protocols. Two protocols under flotation time extensions (>20 min) are analysed, which favour steady recoveries to be obtained at the end of the process. Agar’s criterion is used to evaluate the consistency between the maximum recovery obtained by regression and the total measured recoveries. A good agreement is observed under critical flotation times (tcrit) lower than 40% of the total flotation time, where tcrit corresponds to the time at which the incremental concentrate grade equals the feed grade (grinding product).A discretized ER is used as an approximation of instantaneous ER to characterize the evolution of the enrichment along the process. This discrete ER is defined as the ratio between the incremental concentrate grade and the grade of the solid in the flotation cell prior to the respective flotation interval. Discrete ERs greater than 1 along with significant discrete recoveries are feasible, suggesting that further analyses are required to evaluate the process exhaustion. Four size-by-size tests are also studied to assess the distribution of the discrete ERs at long flotation times. Almost all the evaluated classes present discrete ERs greater than 1 in the last flotation intervals. Therefore, the non-selective mechanisms (i.e., entrainment, true flotation of gangue and gangue association) cannot be considered as the predominant contributions to the overall discrete recoveries. Exceptions may be laboratory tests under very fast kinetic responses, high mass recoveries, long flotation times and high content of non-floatable valuable minerals.

High extent mass recovery of alginate hydrogel beads network based on immobilized bio-sourced porous carbon@Fe3O4-NPs for organic pollutants uptake

This work goes inside the understanding of organic pollutants adsorption mechanism over network alginate hydrogel beads based on immobilized bio-sourced PC@Fe3O4-NPs (PC@Fe3O4-NPs@Alginate) and highlights its high extent mass recovery in aqueous media. The samples were successfully synthesized, we previously developed porous carbon (PC), which, was used to elaborate PC@Fe3O4-NPs via simple in situ coprecipitation (PC@ Fe3O4-NPs), which was encapsulated by alginate-Ca2+ via the blend crosslinking method. The structural, textural, chemical and morphological proprieties of as prepared materials were studied by XRD, FTIR, Raman spectroscopy, nitrogen adsorption-desorption, XPS, SEM and TEM. The adsorption kinetic and isotherm data were well fitted to the pseudo-second-order and Langmuir models. Magnetic particles exhibited an excellent ability to adsorb methylene blue (MB) from aqueous solutions with maximum MB adsorption capacity of 180.42 mg g−1 (PC@Fe3O4 NPs powder) and 49.66 mg g−1 (beads based PC@Fe3O4-NPs@Alginate). Response surface methodology was used to optimize the removal efficiency of MB from aqueous solution and optimum parameters were determined. Magnetic beads based PC showed good magnetic propriety, long-term stability, regeneration capabilities and high extent mass recovery.

Isolation of Chavibetol and Methyleugenol from Essential Oil of Pimenta pseudocaryophyllus by High Performance Liquid Chromatography.

A high performance liquid chromatography (HPLC) method was developed for the simultaneous isolation, on a semi-preparative scale, of chavibetol and methyleugenol from the crude essential oil of P. pseudocaryophyllus leaves. The purity of the isolated compounds and their quantifications were developed using GC/FID. Chavibetol was isolated with high purity (98.7%) and mass recovery (94.6%). The mass recovery (86.4%) and purity (85.3%) of methyleugenol were lower than those of chavibetol. Both compounds were identified on the basis of spectral analysis. The results suggest that the method can provide chavibetol with high purity, mass recovery, and productivity from crude essential, which will be used in bioassays against stored insect pests.

Tomographic Reservoir Imaging with DNA-Labeled Silica Nanotracers: The First Field Validation.

This study presents the first field validation of using DNA-labeled silica nanoparticles as tracers to image subsurface reservoirs by travel time based tomography. During a field campaign in Switzerland, we performed short-pulse tracer tests under a forced hydraulic head gradient to conduct a multisource-multireceiver tracer test and tomographic inversion, determining the two-dimensional hydraulic conductivity field between two vertical wells. Together with three traditional solute dye tracers, we injected spherical silica nanotracers, encoded with synthetic DNA molecules, which are protected by a silica layer against damage due to chemicals, microorganisms, and enzymes. Temporal moment analyses of the recorded tracer concentration breakthrough curves (BTCs) indicate higher mass recovery, less mean residence time, and smaller dispersion of the DNA-labeled nanotracers, compared to solute dye tracers. Importantly, travel time based tomography, using nanotracer BTCs, yields a satisfactory hydraulic conductivity tomogram, validated by the dye tracer results and previous field investigations. These advantages of DNA-labeled nanotracers, in comparison to traditional solute dye tracers, make them well-suited for tomographic reservoir characterizations in fields such as hydrogeology, petroleum engineering, and geothermal energy, particularly with respect to resolving preferential flow paths or the heterogeneity of contact surfaces or by enabling source zone characterizations of dense nonaqueous phase liquids.

Different transport behaviors of Bacillus subtilis cells and spores in saturated porous media: Implications for contamination risks associated with bacterial sporulation in aquifer

In this study, we compared the transport characteristics of Bacillus subtilis cells and their spores in saturated porous media. Both the bacteria cells and spores were readily transported under lower ionic strengths (IS) (1mM), featuring high mass recovery rates (>75%). The bacteria cells recovery rate declined to 58.05% when the IS increased to 100mM; but the spores recovery rate remained at 74.54%. Spores appear to be more mobile than bacterial cells over wide range of IS. Surface properties and breakthrough curves analysis of the two bio-particles (cells and spores) indicated that attachment, straining and blocking mechanisms contribute differently to deposition processes. The extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory further indicated that the particles attachment may primarily occurred at the secondary energy minimum. More important, XDLVO calculations showed that the dominant forces changed with IS, altering the efficiency of particles attachment. The electric double layer repulsion mainly controlled particle deposition at 1mM. In contrast, the van der Waals attraction and Lewis acid-base interactions dominated particle deposition at 100mM. This study showed that spores are more mobile than bacteria cells in subsurface environment. Given that spores form under harsh environmental conditions, we must consider spore formation and transport when groundwater microbial contamination occurs.

The preparation of high-capacity boronate affinity adsorbents by surface initiated reversible addition fragmentation chain transfer polymerization for the enrichment of ribonucleosides in serum

Boronate affinity adsorption is uniquely selective for cis-diol-containing molecules. The preparation and application of boronate affinity materials has attracted much attention in recent years. In this work, a high-capacity boronate affinity adsorbent was prepared by surface-initiated reversible addition–fragmentation chain transfer polymerization (SI-RAFT). Commercial aminated poly(glycidyl methacrylate) (PGMA) microspheres were modified with the chain transfer agent (CTA) S-1-dodecyl-S-(α,α-dimethyl-α-acetic acid)trithiocarbonate (DDATC). Boronate-affinity adsorbents were then prepared via SI-RAFT polymerization employing 3-acrylamidophenylboronic acid (AAPBA) as the monomer. The Fourier transform infrared spectroscopy (FT-IR), nitrogen adsorption and desorption measurements have proven the successful grafting of AAPBA on PGMA microspheres surface. The boronate affinity adsorbents thus prepared possess much higher adsorption capacity (99.2 µmol/g of adenosine) and both faster adsorption and desorption speed towards ribonucleosides, the adsorption and desorption could be completed in 2 min. The high selectivity of the adsorbents to ribonucleosides was verified in the presence of a large excess of deoxynucleosides. The boronate affinity adsorbents were then employed for sample pretreatment before HPLC analysis of ribonucleosides in serum. The ribonucleosides were effectively enriched by boronate affinity dispersive solid-phase extraction (BA-DSPE), with high mass recoveries and good precision. The simultaneous determination of uridine and guanosine in calf serum was achieved by utilizing the standard addition method, their contents were determined to be 170 ± 11.6 ng/mL and 39.6 ± 4.4 ng/mL respectively. The results proved that the prepared boronate affinity materials could be applied for sample pretreatment of cis-diol containing molecules in biological samples.

Preparative isolation and characterization of monoterpene isomers present in the citral-rich essential oil of Pectis brevipedunculata

In Brazil, many plant species are known as lemongrass due to the citric fragrance of their volatile compounds. Pectis brevipedunculata is a Brazilian ornamental aromatic grass with a ‘lemongrass odor’. To investigate this native Brazilian plant, fresh aerial parts were subjected to hydrodistillation (HD) and solid phase microextraction (SPME). The major compounds (>91.0%) separated by HD were the aldehydes neral and geranial. The chromatographic profile of volatile SPME fractions showed that monoterpenes were the major components, especially α-pinene and limonene. Countercurrent chromatography was used for the preparative isolation of citral (780 mg, >98.7% purity) and geraniol (8 mg, 86.0% purity). In addition, neral (7 mg, 87.5% purity) and geranial (12 mg, 91.0% purity) were purified by high-speed counter-current chromatography (HSCCC). This work demonstrates that P. brevipedunculata is a potential source of citral and HSCCC is a useful tool for separating essential oil components with high purity and mass recovery.

High pH Solubilization and Chromatography-Based Renaturation and Purification of Recombinant Human Granulocyte Colony-Stimulating Factor from Inclusion Bodies

Recombinant human granulocyte colony-stimulating factor (rhG-CSF) is a very efficient therapeutic protein drug which has been widely used in human clinics to treat cancer patients suffering from chemotherapy-induced neutropenia. In this study, rhG-CSF was solubilized from inclusion bodies by using a high-pH solution containing low concentration of urea. It was found that solubilization of the rhG-CSF inclusion bodies greatly depended on the buffer pH employed; alkalic pH significantly favored the solubilization. In addition, when small amount of urea was added to the solution at high pH, the solubilization was further enhanced. After solubilization, the rhG-CSF was renatured with simultaneous purification by using weak anion exchange, strong anion exchange, and hydrophobic interaction chromatography, separately. The results indicated that the rhG-CSF solubilized by the high-pH solution containing low concentration of urea had much higher mass recovery than the one solubilized by 8M urea when using anyone of the three refolding methods employed in this work. In the case of weak anion exchange chromatography, the high pH solubilized rhG-CSF could get a mass recovery of 73%. The strategy of combining solubilization of inclusion bodies at high pH with refolding of protein using liquid chromatography may become a routine method for protein production from inclusion bodies.

Fast preparation of recombinant human stem cell factor from inclusion bodies using different hydrophobic interaction chromatographic columns

A method was developed to increase the recovery of recombinant human stem cell factor (rhSCF) from inclusion bodies using high performance hydrophobic interaction chromatography (HPHIC). The target protein was first solubilized in 8.0 mol/L urea solution, and was purified and refolded simultaneously by HPHIC with different chromatographic cakes. Experimental conditions, such as the ligand structures of stationary phase and the composition of mobile phase, were optimized. Under the optimal conditions, high mass recoveries and specific activities of rhSCF were acquired, the purities of rhSCF were above 95.5%, and the mass recoveries of rhSCF were above 49.6%. The final product was also verified as monomer by size exclusion chromatography and matrix assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF-MS). These results provided further evidence that HPHIC is an effective tool in the refolding and purification of recombinant proteins.

Isolation of chavibetol from essential oil of Pimenta pseudocaryophyllus leaf by high-speed counter-current chromatography

Counter-current chromatography (CCC) was used to isolate chavibetol from the essential oil of leaves of Pimenta pseudocaryophyllus (Gomes) Landrum. Chavibetol was obtained in high purity (98%) and mass recovery (94.4%). Methyleugenol was also isolated. The CCC biphasic solvent system used was composed of hexane: n-butanol:methanol:water (12:4:4:3, v/v/v/v).

Novel tetrazole-functionalized ion exchanger for weak cation-exchange chromatography of proteins

A new type of weak cation exchanger, tetrazole-functionalized silica, was developed for bioseparation. It was prepared conveniently by modifying silica gel initially with γ-glycidoxypropyltrimethoxysilane, then with 3-hydroxypropionitrile and finally with ammonium-catalyzed (3 + 2) azide–nitrile cycloaddition, which is an element of click chemistry. The prepared stationary phase was characterized and evaluated for its separation performance, protein retention behavior, loading capacity, protein recovery and chemical stability. The results show that the stationary phase developed has excellent performance for protein separations with high mass recoveries, and has long-term stability. Some remarkable differences were observed between this new exchanger and a carboxylic methyl-functionalized ion exchanger, which is typically used in weak cation-exchange chromatography of proteins. The obtained column was also used for the purification of lysozyme from chicken egg white, and the purity and specific bioactivity of the obtained lysozyme were about 90% and 67 IU/mg, respectively.

Hydrophobic Interaction Chromatography of a Fosfomycin-Modified Zirconia Support for Some Basic Proteins

In this study, we explored the use of fosfomycin modified microparticulate zirconia (FZ) as a novel hydrophobic interaction chromatography (HIC) stationary phase for proteins separation. The results showed that on the FZ stationary phase, the basic proteins such as lysozyme, ribonuclease-A, and a-chymotrypsin, presented a retention mechanism that well agreed with the theory of hydrophobic interaction. The undesirable cation exchange and ligand exchange interactions that usually resulted from the complex surface chemistry of zirconia matrix, could be effectively suppressed due to the phosphonate modification and moderately high salt concentration used in the mobile phases. A few basic proteins achieved good separations by the gradient elution mode with decreasing salt concentration, and high mass recoveries, as well as loading capacity for these proteins obtained on the FZ column. This demonstrates that the FZ stationary phase would be a complement for biocompatible HIC materials, especially for basic proteins, and allows zirconia based supports are more useful for bio-separation.