Unraveling the Complex Composition of Produced Water by Specialized Extraction Methodologies.

Produced water (PW), a waste byproduct of oil and gas extraction, is a complex mixture containing numerous organic solubles and elemental species; these constituents range from polycyclic aromatic hydrocarbons to naturally occurring radioactive materials. Identification of these compounds is critical in developing reuse and disposal protocols to minimize environmental contamination and health risks. In this study, versatile extraction methodologies were investigated for the untargeted analysis of PW. Thin-film solid-phase microextraction with hydrophilic-lipophilic balance particles was utilized for the extraction of organic solubles from eight PW samples from the Permian Basin and Eagle Ford formation in Texas. Gas chromatography-mass spectrometry analysis found a total of 266 different organic constituents including 1,4-dioxane, atrazine, pyridine, and PAHs. The elemental composition of PW was evaluated using dispersive solid-phase extraction followed by inductively coupled plasma-mass spectrometry, utilizing a new coordinating sorbent, poly(pyrrole-1-carboxylic acid). This confirmed the presence of 29 elements including rare earth elements, as well as hazardous metals such as Cr, Cd, Pb, and U. Utilizing chemometric analysis, both approaches facilitated the discrimination of each PW sample based on their geochemical origin with a prediction accuracy above 90% using partial least-squares-discriminant analysis, paving the way for PW origin tracing in the environment.

Reversible chelating polymer for determination of heavy metals by dispersive micro solid-phase extraction with ICP-MS.

N-functionalization of pyrrole with carbon disulfide and subsequent chemical polymerization resulted in the development of a new sorbent material for the extraction of metals. The synthesized polymer, poly(pyrrole-N-carbodithioic acid) (PPy-CS2), is an air-stable, granular powder that is insoluble in water. PPy-CS2 combines pH-dependent chelation, extraction, and desorption sorbent properties that are exploited for the selective extraction and sensitive determination of heavy metals in water matrices using ultrasound-assisted dispersive micro solid-phase extraction and inductively coupled plasma mass spectrometry. Excellent removal and recovery of Cd(II), Co(II), Cu(II), Ni(II), Pb(II), and Zn(II) were achieved and compared with unfunctionalized polypyrrole, which demonstrated extraction resulted from chelation of the metal ions. The extraction efficiency of the PPy-CS2 sorbent as a function of pH, amount of sorbent, extraction time, and flow rate of the desorption solution were evaluated. Limits of detection ranged from 0.3 for cadmium to 11.2 ng/L for zinc with linear dynamic ranges from 0.1 to 500 µg/L and relative standard deviations from 2.2 to 6.3%. The sample preparation method was successfully applied for determination of the target metals in raw well water, treated well water, and river water. Validation was performed by analysis of a certified reference standard for trace metals in drinking water. Graphical abstract Schematic representation of the ultrasound-assisted micro solid-phase extraction protocol for the removal and recovery of heavy metals by the air-stable, granular, and reversible chelating polymer, poly (pyrrole-N-carbodithioic acid).

Biomimetic coating of bisphosphonate incorporated CDHA on Ti6Al4V.

Bi-functional coatings of carbonated calcium deficient hydroxyapatite (CDHA) on Ti alloys were developed by using a biomimetic coating process. The bi-functionality was achieved by loading alendonate sodium (AS), an approved bisphosphonate drug used for the treatment of osteoporosis, into the inner layers of CDHA coatings. Three possible methods of loading AS into CDHA coatings were systematically studied and compared. The results indicated that the co-precipitation method had greater benefits and can modify the release profile of AS by incorporating AS in the inner layers of the coatings. As a preliminary study, the influences of applied AS dosage to CDHA coatings were evaluated using XRD and SEM. In vitro tests indicated that the AS content on CDHA coatings played a significant role, and optimum AS content in local area is beneficial for osteoblast cells proliferation. It is expected that the CDHA-AS coatings via the co-precipitation approach have potential for bone tissue engineering applications.

Fused Filament Fabrication (Three-Dimensional Printing) of Amorphous Magnesium Phosphate/Polylactic Acid Macroporous Biocomposite Scaffolds.

The ultimate goal of this paper is to develop novel ceramic-polymer-based biocomposite orthopedic scaffolds with the help of additive manufacturing. Specifically, we incorporate a bioceramic known as amorphous magnesium phosphate (AMP) into polylactic acid (PLA) with the help of the melt-blending technique. Magnesium phosphate (MgP) was chosen as the bioactive component as previous studies have confirmed its favorable biomaterial properties, especially in orthopedics. Special care was taken to develop constant diameter AMP-PLA composite filaments, which would serve as feedstock for a fused filament fabrication (FFF)-based three-dimensional (3D) printer. Before the filaments were used for FFF, a thorough set of characterization protocols comprising of phase analysis, microstructure evaluations, thermal analysis, rheological analysis, and in vitro degradation determinations was performed on the biocomposites. Scanning electron microscopy (SEM) results confirmed a homogenous dispersion of AMP particles in the PLA matrix. Rheological studies demonstrated good printability behavior of the AMP-PLA filaments. In vitro degradation studies indicated a faster degradation rate in the case of AMP-PLA filaments as compared to the single phase PLA filaments. Subsequently, the filaments were fed into an FFF setup, and tensile bars and design-specific macroporous AMP-PLA scaffolds were printed. The biocomposite exhibited favorable mechanical properties. Furthermore, in vitro cytocompatibility results revealed higher pre-osteoblast cell attachment and proliferation on AMP-PLA scaffolds as compared to single-phase PLA scaffolds. Altogether, this study provides a proof of concept that design-specific bioactive AMP-PLA biocomposite scaffolds fabricated by FFF can be potential candidates as medical implants in orthopedics.

Synthesis and Characterization of Poly(pyrrole-1-carboxylic acid) for Preconcentration and Determination of Rare Earth Elements and Heavy Metals in Water Matrices.

Pyrrole was N-functionalized with solid carbon dioxide followed by chemical polymerization to create a new air-stable, granular, and water-insoluble sorbent, poly(pyrrole-1-carboxylic acid) (PPy-CO2). PPy-CO2 exhibited enhanced affinity for the sorption of metal ions compared to unfunctionalized PPy due to the incorporation of carboxylate functional groups directly onto the polymer backbone. As a freestanding sorbent material, immobilization to an additional solid support is not needed. Sorption, and therefore preconcentration, occurs simultaneously to achieve efficient removal and recovery of metal ions by a pH-dependent sorption-desorption mechanism. PPy-CO2 was evaluated on the analytical scale for the solid-phase extraction of a range of metal ions and found to efficiently preconcentrate rare earth elements (REEs), Th, and heavy metals (Cr, Fe, Cd, and Pb), which allowed quantitation by inductively coupled plasma mass spectrometry (ICP-MS). The impact of sorption parameters, such as solution pH, amount of sorbent, and sorption time, and the effect of desorption flow rate for recovery were investigated and optimized using ultrasound-assisted dispersive solid-phase extraction (UAD-SPE) with ICP-MS analysis. Maximum efficiency for sorption and recovery of most metal ions was achieved at a solution pH of 6.0, 10 mg of sorbent, a sorption time of 5 min, and desorption conditions of 1 mL of 2 M nitric acid applied at a flow rate of 0.25 mL min-1. Detection limits for REEs and Th ranged from 0.2-3.4 ng L-1 for REEs and Th and 0.9-5.7 ng L-1 for heavy metals. Linear ranges from 0.1-1000 µg L-1 for REEs and 0.1-500 µg L-1 for heavy metals and Th were also observed. PPy-CO2 successfully preconcentrated and facilitated the determination of the targeted metal ions in water matrices of varying complexity, including tap water, well water, river water, and produced water samples. These results indicate the potential application of PPy-CO2 for larger-scale recovery and removal of valuable or hazardous metal ions.

Improved polymerization and depolymerization kinetics of poly(ethylene terephthalate) by co-polymerization with 2,5-furandicarboxylic acid.

Poly(ethylene terephthalate) (PET), known for its clarity, food safety, toughness, and barrier properties, is a preferred polymer for rigid packaging applications. PET is also one of the most recycled polymers worldwide. In light of climate change, significant efforts are underway to improve the carbon footprint of PET by synthesizing it from bio-based feedstocks. Often times, specific applications demand PET to be copolymerized with other monomers. This work focuses on copolymerization of PET with a bio-based co-monomer, 2,5-furandicarboxylic acid (FDCA) to produce the copolyester (PETF). We report the multifunction of FDCA to influence the esterification reaction kinetics and the depolymerization kinetics (via alkaline hydrolysis) of the copolyester PETF. NMR spectroscopy and titrimetric studies revealed that copolymerization of PET with different levels of FDCA improved the esterification reaction kinetics by enhancing the solubility of monomers. During the alkaline hydrolysis, the presence of FDCA units in the backbone almost doubled the PET conversion and monomer yield. Based on these findings, it is demonstrated that the FDCA facilitates the esterification, as well as depolymerization of PET, and potentially enables reduction of reaction temperatures or shortened reaction times to improve the carbon footprint of the PET synthesis and depolymerization process.

Sustainable Animal Protein-Intermeshed Epoxy Hybrid Polymers: From Conquering Challenges to Engineering Properties.

The presence of highly modifiable chemical functional groups, abundance of functional groups, and their biological origin make proteins an important class of biomaterials from a fundamental science and applied engineering perspective. Hence, the utilization of proteins from the animal rendering industry (animal protein, AP) for high-value, nonfeed, and nonfertilizer applications is intensely pursued. Although this leads to the exploration of protein-derived plastics as a plausible alternative, the proposed methods are energy-intensive and not based on protein in its native form, which leads to high processing and production costs. Here, we propose, for the first time, novel pathways to develop engineered hybrid systems utilizing AP in its native form and epoxy resins with mechanical properties ranging from toughened thermosets to elastic epoxy-based systems. Furthermore, we demonstrate the capability to engineer the properties of epoxy-AP hybrids from high-strength hybrids to elastic films through controlling the interaction, hydrophilicity, as well as the extent of cross-linking and network density. Through the facile introduction of cochemicals, a sevenfold increase in the mechanical properties of the conventional epoxy-AP hybrid is achieved. Similarly, because of better compatibility afforded by the similar hydrophilicity, AP demonstrated higher cross-linking capability with a water-soluble epoxy (WEP) matrix, resulting in an elastic WEP-AP hybrid without any external aid.

Investigation of Thermal and Thermomechanical Properties of Biodegradable PLA/PBSA Composites Processed via Supercritical Fluid-Assisted Foam Injection Molding.

Bio-based polymer foams have been gaining immense attention in recent years due to their positive contribution towards reducing the global carbon footprint, lightweighting, and enhancing sustainability. Currently, polylactic acid (PLA) remains the most abundant commercially consumed biopolymer, but suffers from major drawbacks such as slow crystallization rate and poor melt processability. However, blending of PLA with a secondary polymer would enhance the crystallization rate and the thermal properties based on their compatibility. This study investigates the physical and compatibilized blends of PLA/poly (butylene succinate-co-adipate) (PBSA) processed via supercritical fluid-assisted (ScF) injection molding technology using nitrogen (N2) as a facile physical blowing agent. Furthermore, this study aims at understanding the effect of blending and ScF foaming of PLA/PBSA on crystallinity, melting, and viscoelastic behavior. Results show that compatibilization, upon addition of triphenyl phosphite (TPP), led to an increase in molecular weight and a shift in melting temperature. Additionally, the glass transition temperature (Tg) obtained from the tanδ curve was observed to be in agreement with the Tg value predicted by the Gordon⁻Taylor equation, further confirming the compatibility of PLA and PBSA. The compatibilization of ScF-foamed PLA⁻PBSA was found to have an increased crystallinity and storage modulus compared to their physically foamed counterparts.

Polycaprolactone nanofiber interspersed collagen type-I scaffold for bone regeneration: a unique injectable osteogenic scaffold.

There is an increasing demand for an injectable cell coupled three-dimensional (3D) scaffold to be used as bone fracture augmentation material. To address this demand, a novel injectable osteogenic scaffold called PN-COL was developed using cells, a natural polymer (collagen type-I), and a synthetic polymer (polycaprolactone (PCL)). The injectable nanofibrous PN-COL is created by interspersing PCL nanofibers within pre-osteoblast cell embedded collagen type-I. This simple yet novel and powerful approach provides a great benefit as an injectable bone scaffold over other non-living bone fracture stabilization polymers, such as polymethylmethacrylate and calcium content resin-based materials. The advantages of injectability and the biomimicry of collagen was coupled with the structural support of PCL nanofibers, to create cell encapsulated injectable 3D bone scaffolds with intricate porous internal architecture and high osteoconductivity. The effects of PCL nanofiber inclusion within the cell encapsulated collagen matrix has been evaluated for scaffold size retention and osteocompatibility, as well as for MC3T3-E1 cells osteogenic activity. The structural analysis of novel bioactive material proved that the material is chemically stable enough in an aqueous solution for an extended period of time without using crosslinking reagents, but it is also viscous enough to be injected through a syringe needle. Data from long-term in vitro proliferation and differentiation data suggests that novel PN-COL scaffolds promote the osteoblast proliferation, phenotype expression, and formation of mineralized matrix. This study demonstrates for the first time the feasibility of creating a structurally competent, injectable, cell embedded bone tissue scaffold. Furthermore, the results demonstrate the advantages of mimicking the hierarchical architecture of native bone with nano- and micro-size formation through introducing PCL nanofibers within macron-size collagen fibers and in promoting osteoblast phenotype progression for bone regeneration.

Fabrication aspects of PLA-CaP/PLGA-CaP composites for orthopedic applications: a review.

For several decades, composites made of polylactic acid-calcium phosphates (PLA-CaP) and polylactic acid-co-glycolic acid-calcium phosphates (PLGA-CaP) have seen widespread uses in orthopedic applications. This paper reviews the fabrication aspects of these composites, following the ubiquitous materials science approach by studying "processing-structure-property" correlations. Various fabrication processes such as microencapsulation, phase separation, electrospinning, supercritical gas foaming, etc., are reviewed, with specific examples of their applications in fabricating these composites. The effect of the incorporation of CaP materials on the mechanical and biological performance of PLA/PLGA is addressed. In addition, this paper describes the state of the art on challenges and innovations concerning CaP dispersion, incorporation of biomolecules/stem cells and long-term degradation of the composites.

Elastic properties and morphology of individual carbon nanofibers.

The structural complexity of vapor-grown carbon nanofibers means that they require a method that determines both their elastic properties and their corresponding morphology. A three-point bending test method was developed combining atomic force microscopy, transmission electron microscopy (TEM) and focused ion beam techniques to suspend individual nanofibers and measure their deflection coupled with accurate determinations of inner and outer diameters and morphology using high resolution TEM. This resulted in much improved accuracy and reproducibility of the measured values of the elastic modulus which ranged from 6 to 207 GPa. The data showed two distinct trends, with higher values of the modulus when the outer wall thickness of the nanofibers is larger than that of the inner wall, with the values decreasing with the overall wall thickness. These results suggest that the more ordered layers of the outer wall, closest to the inner wall, are mostly responsible for the nanofiber strength. For large nanofiber wall thicknesses of greater than 80 nm, the elastic modulus becomes independent of the thickness with a value of approximately 25 GPa. The results also demonstrate that this technique can be a standardized one for the detailed study of mechanical properties of nanofibers and their relationship to morphology.