Diatomaceous Earth Particles Research Articles

Tailored chitosan integration in diatomaceous earth particles as a scaffold for fructosyltransferase immobilization in fructo-oligosaccharide production.

Fructo-oligosaccharide (FOS) belongs to the group of short inulin-type fructans and is one of the most important non-digestible bifid-oligosaccharides capable of biotransforming sucrose using fructosyltransferase (FTase). However, there are no immobilized FTase products that can be successfully used industrially. In this study, diatomite was subjected to extrusion, sintering and granulation to form diatomaceous earth particles that were further modified via chitosan aminomethylation for modification. FTase derived from Aspergillus oryzae was successfully immobilized on the modified support via covalent binding. The immobilized enzyme activity was 503 IU g-1 at an enzyme concentration of 0.6 mg mL-1, immobilization pH of 7.0 and contact time of 3 h. Additionally, the immobilization yield was 56.91%. Notably, the immobilized enzyme was more stable under acidic conditions. Moreover, the half-life of the immobilized enzyme was 20.80 and 10.96 times as long as that of the free enzyme at 45 and 60 °C, respectively. The results show good reusability, as evidenced by the 84.77% retention of original enzyme activity after eight cycles. Additionally, the column transit time of the substrate was 35.56 min when the immobilized enzyme was applied in a packed-bed reactor. Furthermore, a consistently high FOS production yield of 60.68% was achieved and maintained over the 15-day monitoring period. Our results suggest that immobilized FTase is a viable candidate for continuous FOS production on an industrial scale. © 2024 Society of Chemical Industry.

Diatomaceous earth as insecticide: physiological and morphological evidence of its underlying mechanism.

Wheat grain containers or silos can be perfect habitats for insects, which generate large economic losses to grain production. Natural alternatives to synthetic insecticides have grown in popularity because of health, economic and ecological issues. Diatomaceous earth is a natural compound that has an insecticide effect by enhancing an insect's dehydration with no toxicity on mammals including humans. The aim of this study is to confirm the effect of diatomaceous earth as an insecticide for the wheat grain pest, the red flour beetle Tribolium castaneum (Coleoptera: Tenebrionidae) and demonstrate its underlying mechanisms as an insecticide by open-flow respirometry and scanning electron microscopy. Survival bioassays of T. castaneum revealed a dose-dependent insecticide effect of diatomaceous earth. Gravimetric measurements showed that 2 days exposure to diatomaceous earth produces a significant increase of mass loss. Open-flow respirometry measurements showed an increase of total water emission rate on insects due to an increase of both, respiratory and cuticular water loss. Our study revealed that diatomaceous earth produces an increase of insect's cuticle permeability, which is responsible for elevated cuticular water loss. Scanning electron microscopy images provided visual evidence of the lipid absorbent properties of diatomaceous earth particles, and showed a tendency for higher, although not significant, damaged area of the cuticle's surface from diatomaceous earth treated insects compared to control ones. With state-of-the art techniques like open-flow respirometry and scanning electron microscopy, we demonstrated the underlying mechanism of diatomaceous earth as an insecticide and provided new cues for understanding the properties of the cuticle and its ecological importance. © 2024 Society of Chemical Industry.

A comprehensive approach to simulation of cartridge filtration using CFD

Household water treatment (HWT) systems are widely used for the provision of potable water in many countries with their low-cost key to attaining universal and equitable access to safe and affordable drinking water, Sustainable Development Goal 6.1. Removal of suspended particles (turbidity) from water sources via cartridge filters is often the first step of a HWT system, with the primary treatment increasing the efficiency of a subsequent disinfection step.Whilst the performance of cartridge filters (removal efficiency and pressure drop) can be determined experimentally in long experiments with high volumes of water, numerical simulation adds fundamental insight to the influence of fluid dynamics on particle deposition and vice versa. In this study, a novel computational fluid dynamic (CFD) model was developed to simulate the fundamental mechanisms underpinning the removal of particles within the widely used 10 in. cartridge filter, informed by and complemented with laboratory validation. The Eulerian approach was used to simulate fluid flow with the Lagrangian approach adopted for particle tracking. Rosin-Rammler distribution was implemented with respect to the particle size distribution of the diatomaceous earth particles used in the experiments. Given particles were non-spherical (disk shape), Wadell’s sphericity was included to account for the effect of particle shape on drag force. A porous domain was implemented to simulate the filter element through addition of a source term to the momentum equations, with the likelihood of particle deposition, detachment and rebound also considered.Laboratory based validation studies confirmed the novel CFD model to accurately model removal of turbidity and predict the pressure drop across the filter with Root Mean Square Percentage Error (RMSPE) of less than 3%. The simulated location of particle deposition on the filter elements closely matched images taken at several stages during filtration experiments with the model aiding understanding of pattern of particle removal along and within the porous filter structure. This novel and comprehensive modelling methodology can be utilized to simulate the filtration process at the macro-scale, permitting evaluation of new filter designs and materials for advanced filtration systems; ultimately improving HWT system performance and reducing costs to users.

Selective separation of dye/salt mixture using diatomite-based sandwich-like membrane

A novel nanofiltration membrane was developed by entrapping a layer of modified diatomaceous earth between two layers of electrospun polysulfone (E-PSf) nanofibers. The diatomaceous earth particles and the fabricated membrane were characterized using FTIR, SEM, EDS, zeta potential, and water contact angle techniques. The static adsorption and dynamic separation of pristine E-PSF and sandwich-like membranes for methylene blue (MB) with/without salt were investigated under different operating conditions. The Langmuir model suited the MB adsorption isotherm data with a linear regression correlation coefficient (R2) >0.9955. As pH increased, both flux and MB rejection of the sandwich-like membrane improved by up to 183.8 LMH and 99.7%, respectively, when operated under gravity. The water flux of the sandwich-like membrane was sharply increased by increasing the pressure up to 19,518.2 LMH at 4.0 bar. However, this came at the expense of MB rejection (10.93%) and reduced its practical impact. At a high salt concentration, the sandwich-like membrane also indicated remarkable dye/salt separation with a higher permeation of salt (<0.2% NaCl rejection) and MB rejection (>99%). The performance of the regenerated diatomaceous material and membrane was maintained during five cycles of operation compared to that of the original ones.

Enhanced oil-spill removal and recovery from water bodies using diatomaceous earth and C18-silane-grafted polyurethane

This research focuses on the novel synthesis of polyurethane (PU) foam surface functionalized with diatomaceous earth (DE) particles and non-fluoro octadecylsilane (C18), for the use in enhanced clean-up of oil spill contaminants from water. The modified PU foam has improved hydrophobicity, wettability, water repellency, and biodegradability, which eliminates some of the drawbacks of PU such as its hygroscopic nature, limited hydrophobicity, ecotoxicity, and less biodegradability. The modified PU foam has been characterized by scanning electron microscopy to understand the microstructural changes during the surface modifications, Fourier transform infrared spectroscopy to track the integration of functional groups, X-ray crystallographic study to indicate the increase in the crystallinity of the resultant foam due to the incorporation of silane, and thermogravimetric analysis to understand the thermal stability and to calculate the thermal mass loss during the chemical modification. Furthermore, to test the enhanced hydrophobicity and oil spill clearance from water, the water contact angle has been measured and crude oil absorption capacity has been tested. The results show increased water repellency attributed to the strong hydrophobicity, and about 2.13 folds of increased crude oil absorption in comparison to the unmodified PU foam. Hence, the results collectively suggest the use of the synthesized surface-modified PU foam with superior hydrophobicity, water repellence, and surface wettability as a potential candidate for enhanced crude oil absorption from water bodies. Graphical abstract

Biobased Castor Oil-Based Polyurethane Foams Grafted with Octadecylsilane-Modified Diatomite for Use as Eco-Friendly and Low-Cost Sorbents for Crude Oil Clean-Up Applications.

Herein we report the synthesis and characterization of novel castor oil-based polyurethane (PU) foam functionalized with octadecyltrichlorosilane (C18)-modified diatomaceous earth (DE) particles, exhibiting superior hydrophobicity and oil adsorption, and poor water absorption, for use in effective clean-up of crude oil spillage in water bodies. High-performance and low-cost sorbents have a tremendous attraction in oil spill clean-up applications. Recent studies have focused on the use of castor oil as a significant polyol that can be used as a biodegradable and eco-friendly raw material for the synthesis of PU. However, biobased in-house synthesis of foam modified with C18-DE particles has not yet been reported. This study involves the synthesis of PU using castor oil, further modification of castor oil-based PU using C18 silane, characterization studies and elucidation of oil adsorption capacity. The FTIR analysis confirmed the fusion of C18 silane particles inside the PU skeleton by adding the new functional group, and the XRD study signified the inclusion of crystalline peaks in amorphous pristine PU foam owing to the silane cross-link structure. Thermogravimetric analysis indicated improvement in thermal stability and high residual content after chemical modification with alkyl chain moieties. The SEM and EDX analyses showed the surface's roughness and the incorporation of inorganic and organic elements into pristine PU foam. The contact angle analysis showed increased hydrophobicity of the modified PU foams treated with C18-DE particles. The oil absorption studies showed that the C18-DE-modified PU foam, in comparison with the unmodified one, exhibited a 2.91-fold increase in the oil adsorption capacity and a 3.44-fold decrease in the water absorbing nature. From these studies, it is understood that this novel foam can be considered as a potential candidate for cleaning up oil spillage on water bodies.

Bio-Based Porous Aerogel with Bionic Structure and Hydrophobic Polymer Coating for Efficient Absorption of Oil/Organic Liquids.

Increasing contamination risk from oil/organic liquid leakage creates strong demand for the development of absorbents with excellent hydrophobicity and absorption capacity. Herein, bagasse was carbonized to form porous char with a special structure of array-style and vertically perforated channels, and then the activation process enlarged the pore volume of the char. With the cooperation of low-surface-energy polydimethylsiloxane and diatomaceous earth particles, the modified activated carbon aerogel (MACA) was fabricated by modifying the surface coating and mastoid structure on the bagasse char. Moreover, the MACA demonstrates high porosity oil-water separation, hydrophobicity, and considerable absorption capacity (4.06-12.31 g/g) for gasoline and various organic solvents. This work converts agricultural waste into an efficient porous adsorbent, offering a scalable and commercially feasible solution to solving the leakages of oil/organic solvents.

Application of nano remediation of mine polluted in acid mine drainage water using machine learning model

Acid mine drainage (AMD) is the term used to describe drainage from coal mines with high sulfur-bearing rocks. The oxidative weathering of metal sulfides leads to AMD. The acidic environment corrodes more harmful compounds in the soil, which is spread throughout the working area. One such significant metal is copper, which is extracted in massive quantities from ores rich in sulfide. A copper-extraction resin might be created by combining diatomaceous earth (DE) particles with polyethyleneimine (PEI), which is shown to have great selectivity and affinity for copper. In this effort, PEI-DE particles’ copper absorption level was examined by using synthetic and actual acid mine drainage samples at varied pH values. The findings of the copper uptake particles have been examined through the Support Vector Machine (SVM) model. Using the n-fold 14 cross-validation approach, the quantities of parameters and C are estimated to be 0.001 and 0.01, respectively. The SVM analysis was correct, and the findings indicated that copper could bind to the material efficiently and preferentially at pH 4. Subsequent water elution studies at a pH value of 1 confirmed the pH-reliant interaction between dissolved Cu and PEI by demonstrating full release of the adsorbed Cu. In this research, the copper absorption of PEI-DE particles from synthetic and genuine AMD specimens was studied based on several pH conditions. The findings suggest that copper may attach to the material effectively and preferentially at pH 4. Studies of filtering water at pH1 later confirmed that all of the adsorbed Cu was released. This shows that the interaction between PEI and dissolved Cu depends on PH.

Diatomaceous earth as a drug-loaded carrier in a glass-ionomer cement

The effect of a natural filler (diatomaceous earth [DE], a promising drug-delivery agent) and its content was investigated on the performance of a model glass-ionomer cement (GIC). Three sample series, differing in DE content (0, 2.5 and 5 wt%), were prepared using a commercial GIC as a matrix (3M Ketac Molar Easymix). The resultant surface microhardness and roughness, wear performance, and compressive strength of the samples were measured after the samples had been stored in deionized water at 37°C for a fixed time. Moreover, the film thickness was tested for the freshly mixed samples. The numerical data was subjected to statistical analysis, in order to test the null hypotheses of the equality of the measured properties between the reference and the DE-modified samples. According to the results, diatomaceous earth particles are uniformly distributed in the GIC matrix, and the cavities of frustules tend to be filled with the GIC. This translates into the observed performance of the DE-loaded GIC. Compared with the reference material (0 wt% DE), the surface microhardness (2.5 wt% DE, p = 0.014; 5 wt% DE, p = 0.005) and roughness (e.g. Ra; 2.5 wt% DE, p = 0.003; 5 wt% DE, p < 0.001) are increased. No effect on the wear performance (p = 0.530 and 0.256, respectively) or compressive strength (p = 0.514) was noticed in the case of DE partially substituting the glass phase. Based on the study results, it is evidenced that diatom frustules are a suitable filler for application in conventional glass-ionomer cements as the glass-substituting drug-loaded carrier. Notably, however, the surface finish method of the DE-filled materials needs development.

Influence of Diatomaceous Earth Particle Size on Mechanical Properties of PLA/Diatomaceous Earth Composites.

The fractionation of diatomaceous earth (DE) using sedimentation made it possible to obtain separate unbroken diatom fractions from broken or agglomerated bodies with a range of particle sizes. The produced filler was used to prepare polylactide (PLA)/diatomaceous earth biocomposite samples containing different particle sizes, which were subjected to mechanical testing (tensile strength, flexural strength, impact strength), colloidal testing (contact angle, color change test, SEM/EDS), and thermal testing (TGA, DSC, DMA). Modification of the PLA containing the smallest particle size with diatomaceous earth (Fraction 5) resulted in a higher impact strength compared to both the pure PLA and the PLA/DE composite that contained base diatomaceous earth. Furthermore, the melt flow rate was improved by more than 80 and 60% for the composite modified with fractionated diatomaceous earth (Fraction 4) compared to pure PLA and base diatomaceous earth, respectively. The elasticity of the composite was also improved from 3.3 GPa for pure polylactide to 4.4 GPa for the system containing the smallest diatomaceous earth particles (Fraction 5).

One‐step fabrication of wear‐resistant superhydrophobic coating based on aminosilane‐functionalized diatomaceous earth

AbstractFacile fabrication of superhydrophobic coatings with excellent mechanical robustness is highly desired in practical application. Herein, a convenient and effective strategy for one‐step fabrication of robust volumetric superhydrophobic coating was developed containing aminosilane‐functionalized cylindrical diatomaceous earth (DE) particles and a polyurethane (PU) resin. Due to the strong chemical cross‐linking between the amino groups and the isocyanates, the superhydrophobic DE particles were strongly anchored to the PU resin, thus improving the wear resistance of the coating. The coating could withstand 20 m sandpaper abrasion under a constant pressure of 2.6 kPa. The wear resistance of the coating improved nearly 471% compared with the superhydrophobic DE/PU composite coating prepared by physical‐blending. Moreover, the coating also demonstrated great self‐cleaning performance, excellent chemical stability and underwater durability. Additionally, the as‐prepared coating could be easily applied to various substrates and exhibited high rigidity (3H‐4H), good adhesion (4B‐5B), and great flexibility (impact resistance of 1 Kg·m).

Novel 3D printing filament composite using diatomaceous earth and polylactic acid for materials properties and cost improvement

There are a large variety of different materials currently used for producing 3D printing filaments. In this paper we are investigating the utilization of diatomaceous earth as a potential component for polylactic acid based 3D printing composite materials. The results clearly show that with only minor deterioration of the basic mechanical properties of the 3D printed material at least 10 wt% of the polylactic acid usage can be reduced and replaced by diatomaceous earth. Our thermal analysis also shows nucleation and chain mobility phenomena in the presence of diatomaceous earth particles. The results also show that we are able to engineer 3D printing surfaces with diatomaceous earth protruding from the composite structure and thus allowing us to create high surface area on the 3D printed objects surface. With this research we have shown for the first time an opportunity for cost reduction compared to using pure polylactic acid filaments and a pathway to immobilizing chemical sensing, antibacterial and antiviral agents on 3D printed objects for many applications such as biomedical.

Amine activated diatom xerogel hybrid material for efficient removal of hazardous dye

The effective removal of organic pollutants from aqueous media is still an eminent challenge. In the present work, naturally available diatomaceous earth (DE) particles was surface modified with mesoporous silica xerogel denotes as diatom xerogel material. Subsequently amine functionality has been successfully introduced on diatom xerogel (DXEA) for the efficient removal of hazardous dye, Eriochrome Black T (EBT). The adsorbents before and after EBT adsorption were characterized using various techniques such as XRD, FE-SEM, FTIR and BET. The adsorption process was conducted by varying many parameters such as pH, dosage, initial concentration of dye and time. The designed adsorbent, DXEA showed increased removal efficiency (∼99 %) in comparison with neat DE (∼58 %) due to the presence of amine functional group, which favours the rapid adsorption of EBT. This study showed that adsorbent DXEA was adequate to remove 50 mg/L and 100 mg/L of aqueous EBT in 5 and 60 min of contact time respectively. The maximum dye adsorption capacity of DXEA was found to be ∼62 mg/g whereas, for DE it was ∼56 mg/g. The dye adsorption kinetics of EBT onto both the DXEA and the DE follow the pseudo-second-order model. Also, DXEA was used for selective removal of EBT in the presence of other dyes and recycle studies were discussed. These studies showed that DXEA is a promising material for EBT removal by adsorption in real sample.

Phosphate removal by iron oxide-coated diatomite: Laboratory test of a new method for cleaning drainage water

Transport of phosphate (P) in drainage water from P rich agricultural fields to freshwaters via drains may cause open water eutrophication. One way to reduce this transport is by installation of P sorbing filters at drain outlets. As drainage water flows and P concentrations can be highly fluctuating, suitable filters must have good hydraulic conductivity and high P sorbing efficiency, i.e. rapid sorption with high affinity and capacity. To fulfill these requirements, we tested a new concept for filter material design comprising porous and stable calcined diatomaceous earth particles (CDE, 2–4 mm) coated with thin layers of high affinity P sorbing amorphous iron oxide. According to NMR and MICP analyses the material had a bimodal pore size distribution with average diameters of around 1 μm and 100 μm. The coating formed a thin film on the CDE internal and external surfaces and markedly increased the P sorption efficiency. Thus, P in 0.1 and 0.5 mg P/L solutions was almost quantitatively sorbed within 1½ min at a solution:solid ratio of 100. SEM-EDX demonstrated that P quickly penetrated into the porous structure of the CDE granules and that all Fe in the coating was active in P bonding. This conceptual investigation demonstrates that porous CDE is a useful host into which Fe oxides can be precipitated resulting in an effective P sorbing material.

Copper removal from acid mine drainage-polluted water using glutaraldehyde-polyethyleneimine modified diatomaceous earth particles

Mine waters and tailings generated from mining and mineral processing activities often have detrimental impact on the local environment. One example is acid mine drainage, in which sulphides in the mining waste react with water and oxygen to produce an acidic environment that subsequently dissolves host rock minerals from the waste containing toxic metals and trace elements. Copper is one such metal of significance, as it is mined at large volumes in sulphide containing ores. It has strong biocidal activity that greatly affects ecosystems. We have previously reported that glutaraldehyde (GA)-crosslinked polyethyleneimine (PEI) has strong affinity and selectivity for copper and that diatomaceous earth (DE) particles can be modified with the material to form a copper-extraction resin. In this study, the copper uptake of GA-PEI-DE particles was investigated from synthetic and real acid mine drainage samples under different pHs and their copper removal performance was compared with that of selected commercial resins. The results revealed that copper could effectively and preferentially bind to the material at pH 4, and that the copper could be completely eluted by lowering of the pH. In addition, effective copper uptake and elution was demonstrated using real legacy acid mine drainage water from Mount Lyell in Tasmania.

Investigation of the effect of mesoporous diatomaceous earth particles on RATRP of styrene and butyl acrylate

Mesoporous diatomite nanoplatelets were employed to prepare various poly (styrene-co-butyl acrylate)/diatomite nanocomposites by in situ reverse atom transfer radical polymerization of styrene and butyl acrylate. Fourier-transform infrared spectroscopy, thermogravimetric analysis (TGA), and nitrogen adsorption/desorption isotherm were employed for evaluating some properties of the pristine diatomite nanoplatelets. Evaluation of pore size distribution and morphological studies were also performed by scanning and transmission electron microscopy. Conversion and molecular weight determinations were carried out using gas and size exclusion chromatography, respectively. Addition of 3 wt% pristine mesoporous diatomite nanoplatelets leads to an increase in conversion from 77% to 92%. Molecular weight of poly (styrene-co-butyl acrylate) chains increases from 17,348 g mol−1 to 21,346 g mol−1 with the addition of 3 wt% pristine mesoporous diatomite nanoplatelets; however, polydispersity index values increases from 1.38 to 1.65. Increasing thermal stability of the nanocomposites is demonstrated by TGA. Differential scanning calorimetry shows an increase in glass transition temperature from 35.5°C to 39.4°C with the addition of 3 wt% mesoporous diatomite nanoplatelets.

Polyethyleneimine functionalized mesoporous diatomite particles for selective copper recovery from aqueous media

To date, the quest for cost-effective methods for removal of dissolved metals from aqueous solutions remains a daunting challenge for many industries. This paper reports on the development of an effective, hybrid adsorbent for selective copper recovery from aqueous solutions under industrially relevant conditions. The work involved (i) purification and functionalization of diatomaceous earth (DE) particles with glutaraldehyde(GA)-crosslinked polyethyleneimine(PEI), (ii) physicochemical characterization of the product and (iii) metal adsorption from solutions containing Cu(II)/Ni(II)/Fe(II)/Ca(II)/Mg(II)/Mn(II)/Al(III)/Na ions and their subsequent elution behaviour. Acid leaching of the pristine DE led to a significant reduction in its metal oxide (e.g., Al2O3, Fe2O3) constituents and a concomitant increase in both SiO2 content and specific surface area. Upon functionalization with GA-crosslinked PEI, the DE particles' interfacial chemistry was completely altered to that of the polymer with no change in specific surface area. Isothermal batch adsorption from saline (15g/dm3 NaCl) and non-saline solutions containing 500 and 1000mg/dm3 of Cu at ~pH4 revealed >97% Cu(II) removal by functionalized DE within 3min in both cases. Subsequent water elution tests at pH1 showed complete release of the adsorbed Cu confirming pH-dependent interaction between dissolved Cu and GA-crosslinked PEI. The preliminary batch adsorption/elution tests involving 1000mg/dm3 solutions of Ni, Ca, Mg, Mn, Fe, Na and Al showed little or negligible affinity of the functionalized DE towards these elements, suggesting good selectivity for Cu. Furthermore, it is shown that the functionalized particles are chemically stable at H2SO4 concentrations up to 2M and may be recycled >10 times without loss in their Cu adsorption/desorption performance.

Chemodosimeter functionalized diatomaceous earth particles for visual detection and removal of trace mercury ions from water

The rhodamine based receptor, P2 has been developed for the detection of environmentally hazardous Hg2+ ions with a limit of detection, 1.5×10−6M. The P2 showed a significant colour change from colourless to pink upon binding with Hg2+ ions. As a result, a new peak at 533nm was observed in UV–vis spectroscopy which was attributed to spirolactum ring opening followed by through bond energy transfer (TBET). In addition, the presence of other competing cations did not interfere the detection of Hg2+ ions. Further, P2 has been successfully immobilized onto the naturally available and highly porous diatomaceous earth particles (P2D) for removal of Hg2+ ions from water. The covalently attached organic molecule in P2D forms complex with Hg2+ ion present in the water and thus traps the Hg2+ ions. Based on this, a proof-of-concept cartridge has been developed for water purification. The cartridge having 450mg of P2D was able to purify 30mL of water containing 1ppm Hg2+ ions. The efficiency of cartridge could be visualized with a colour change from colourless to pink.

Particle morphology dependent superhydrophobicity in treated diatomaceous earth/polystyrene coatings

Superhydrophobic surfaces have been prepared from three different types of diatomaceous earth (DE) particles treated with 3-(heptafluoroisopropoxy)propyltrimethoxysilane (HFIP-TMS) and low molecular mass polystyrene. The untreated particles, consisting of CelTix DE (disk shape), DiaFil DE (rod shape) and EcoFlat DE (irregular), were studied using particle size analysis, bulk density, pore volume and surface area analysis (via Brunauer–Emmett–Teller, BET, methods). The treated particles were characterized with thermogravimetric analysis (TGA), contact angles, scanning electron microscopy, profilometry, and FTIR spectroscopy. The minimum amount of silane coupling agent on the DE surfaces required to obtain superhydrophobicity of the particles was determined and found to be dependent on the particle morphology. In the coatings made from different particles with 2.4wt% HFIP-TMS, the minimum amounts of treated particles (loadings) for superhydrophobicity was determined with the less dense CelTix DE requiring about 30wt%, DiaFil DE requiring about 40wt%, and EcoFlat DE each requiring about 60wt% loading of treated particles.

Glutaraldehyde‐crosslinking for improved copper absorption selectivity and chemical stability of polyethyleneimine coatings

ABSTRACTNano‐thin coatings of glutaraldehyde (GA)‐crosslinked polyethyleneimine (PEI) are extremely selective and effective in binding copper from seawater. Here it was demonstrated that GA‐PEI performs significantly different from PEI. The copper‐selectivity of self‐assembled PEI coatings on silicon substrates was greatly improved by GA‐crosslinking. After submersion in artificial seawater containing 200 ppb copper and equimolar amounts of 11 competing ions only copper and trace amounts of Zn were detected in the GA‐crosslinked coatings, while for non‐crosslinked PEI there was about 30% Zn present relative to copper. The coatings were demonstrated to be highly stable under acidic conditions and retained their copper‐binding selectivity after repeated cycles of binding and acid‐mediated elution. After self‐assembly of the GA‐crosslinked coating on mesoporous diatomaceous earth particles, significant amounts of copper could be extracted from 200 ppb in artificial seawater and eluted under acidic pH. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 43954.