Synthetic Water-soluble Polymers Research Articles

Simultaneous identification and quantification of three water-soluble polymers (PVP, PNVCL and PEI) in wastewater samples by continuous-flow off-line pyrolysis GC/MS

In environmental analysis, the detection of water-soluble synthetic polymers (WSSP) presents considerable challenges. Thus, a precise and reproducible analytical method was developed using continuous-flow off-line pyrolysis with gas chromatography/mass spectrometry (GC/MS) to simultaneously identify multiple water-soluble polymers from a single environmental sample.WSSP are widely used in multiple industries as hydrogels due to their hydrophilic character and potential biocompatibility. This adaptability of hydrogels is reflected in their ability to provide customized formulations for specific needs, such as in the development of personal care products, medicine, and pharmaceuticals.Specifically, polyvinylpyrrolidone (PVP), poly(N-vinylcaprolactam) (PNVCL), and polyethyleneimine (PEI) were targeted for analysis in wastewater, employing unique pyrolysis products for identification. These polymers require careful assessment in wastewater to evaluate potential environmental risks associated with their release.PVP and PNVCL were identified through two pyrolysis products, while six pyrolysis products were utilized for the identification of PEI.The validated method demonstrated very good linearity and reproducibility, with correlation coefficients ranging from 0.94 to 0.99 and relative standard deviation (RSD) values between 3 % and 36 % for the targeted compounds. The limit of quantification (LOQ) for the three polymers ranged from 1 to 10 μg L-1. Moreover, the average recovery rates for these polymers, determined from artificial water samples, were approx. 85 %.Utilizing the validated method, water samples from seven wastewater treatment plants in Germany were successfully analyzed, confirming the presence of these polymers at elevated concentrations in the μg L-1 range. Notably, untreated influent waters exhibited higher polymer levels compared to treated influents and effluents, underscoring their significant contribution to overall polymer content.The developed analytical method provides an efficient tool for the simultaneous identification and quantification of PVP, PNVCL, and PEI in wastewater samples. The results highlighted the prevalent presence of PVP, PNVCL, and PEI in the tested wastewater samples, indicating their significant abundance.

Deciphering polymer degradation chemistry via integrating new database construction into suspect screening analysis.

Water-soluble synthetic polymers and their environmental degradation products are overlooked but important industrial pollutants in wastewater. However, the detection of degradation products is limited to bulk solution chemistry and molecular-level analysis remains unreachable. In this work, we assessed the feasibility of current suspect screening and nontarget workflow using liquid chromatography-high resolution mass spectrometry (LC-HRMS) to elucidate molecular level information about polyacrylamide (PAM) and its degraded products by free radicals. Radical chain scission of PAM (10 kDa) using heat-activated persulfate was conducted to simulate hydraulic fracturing conditions in the deep subsurface. We found that the current workflows in the commercial software generated predicted formulae with low accuracy, due to limited capability of peak picking and formula prediction for high mass and charge features. By modeling literature-reported degradation pathways, we constructed a degradation product database of over 463 000 unique formulae, which improved the accuracy of the predicted formula. For the matched features, the ratio of aldehyde/ketone terminating molecule abundance was found to increase over 24 h degradation time, suggesting increasing content of aldehydes by radical-induced oxidative chain scission of PAM. This is contradictory to previously proposed ratios of carbon-centered radical position on polymer backbone initiated by hydroxyl radicals. Using in silico fragmentation of MS1 features, we identified 11 structures with confidence levels 2b and 3 using their MS2 information. This is the first attempt to resolve complex polymer degradation chemistry using HRMS that can advance our ability to detect water-soluble polymer pollutants and their transformation products in environmental samples.

Electrospun Nanofibrous Mesh Based on PVA, Chitosan, and Usnic Acid for Applications in Wound Healing.

Injuries and diseases of the skin require accurate treatment using nontoxic and noninvasive biomaterials, which aim to mimic the natural structures of the body. There is a strong need to develop biodevices capable of accommodating nutrients and bioactive molecules and generating the process of vascularization. Electrospinning is a robust technique, as it can form fibrous structures for tissue engineering and wound dressings. The best way of forming such meshes for wound healing is to choose two polymers that complement each other regarding their properties. On the one hand, PVA is a water-soluble synthetic polymer widely used for the preparation of hydrogels in the field of biomedicine owing to its biocompatibility, water solubility, nontoxicity, and considerable mechanical properties. PVA is easy to subject to electrospinning and can offer strong mechanical stability of the mesh, but it is necessary to improve its biological properties. On the other hand, CS has good biological properties, including biodegradability, nontoxicity, biocompatibility, and antimicrobial properties. Still, it is harder to electrospin and does not possess as good mechanical properties as PVA. As these structures also allow the incorporation of bioactive agents due to their high surface-area-to-volume ratio, the interesting point was to incorporate usnic acid into the structure as it is a natural and suitable alternative agent for burn wounds treatment which avoids an improper or overuse of antibiotics and other invasive biomolecules. Thus, we report the fabrication of an electrospun nanofibrous mesh based on PVA, chitosan, and usnic acid with applications in wound healing. The obtained nanofibers mesh was physicochemically characterized by Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). In vitro biological assays were performed to evaluate the antimicrobial properties of the samples using the MIC (minimum inhibitory concentration) assay and evaluating the influence of fabricated meshes on the Staphylococcus aureus biofilm development, as well as their biocompatibility (demonstrated by fluorescence microscopy results, an XTT assay, and a glutathione (GSH) assay).

Determination of the water-soluble polymer poly(ethyleneimine) (PEI) in wastewater by continuous-flow off-line pyrolysis GC/MS

Reliable identification and quantification of water-soluble synthetic polymers (WSSP), such as polyethyleneimine (PEI), is crucial for understanding their potential impact on certain ecological environments. Therefore, this study proposes an analytical method combining on-line and off-line pyrolysis GC/MS to investigate the pyrolytic degradation. mechanism of branched PEI and develop a calibration method using specific pyrolysis. products, including methylpyrazine, dimethylpyrazine, ethylmethylpyrazine, trimethylpyrazine, methylpropylpyrazine and ethyldimethylpyrazine, for the. quantification of PEI in environmental wastewater samples. The developed analytical. method shows adequate linearity for all molecular ions of the specific pyrolysis. products, with a determination coefficient ranging from 0.95 to 0.98 for the range of 10–500 μg PEI. The limit of quantification for this method lies between 1 and 10 μg/L of PEI. The accuracy (absolute recovery 71–95%) and reproducibility (RSD < 30%) were. evaluated by multiple spiking/recovery experiments at a PEI level of 500 μg. Using this. method for samples collected from different wastewater treatment plants in Germany. reveals a significant emission of PEI to the aquatic environment with concentrations. ranging from 0.08 mg L-1–0.55 mg L-1, and thus demonstrating its applicability in. environmental studies. To the best of our knowledge, this is the first report on the. occurrence of PEI in environmental samples.

Visible-light photocatalytic degradation of water-soluble polyvinyl alcohol in aqueous solution by Cu2O@TiO2: Optimization of conditions, mechanisms and toxicity analysis

Polyvinyl alcohol (PVA), a water-soluble synthetic polymer, is one of the most prevalent non-native polyvinyl alcohols found in the environment. Due to its inherent invisibility, its potential for causing severe environmental pollution is often underestimated. To achieve efficient degradation of PVA in wastewater, a Cu2O@TiO2 composite was synthesized through the modification of titanium dioxide with cuprous oxide, and its photocatalytic degradation of PVA was investigated. The Cu2O@TiO2 composite, supported by titanium dioxide, facilitated photocarrier separation and demonstrated high photocatalytic efficiency. Under alkaline conditions, the composite exhibited a 98% degradation efficiency for PVA solutions and a 58.7% PVA mineralization efficiency. Radical capture experiments and electron paramagnetic resonance (EPR) analyses revealed that superoxide radicals primarily drive the degradation process within the reaction system. Throughout the degradation process, PVA macromolecules are broken down into smaller molecules, including ethanol, and compounds containing aldehyde, ketone, and carboxylic acid functional groups. Although the intermediate products exhibit reduced toxicity compared to PVA, they still pose certain toxic hazards. Consequently, further research is necessary to minimize the environmental impact of these degradation products.

Degradation of oligo[poly(ethylene glycol) fumarate] hydrogels through stimulus-mediated pendent group cyclization

Hydrogels are of interest for a wide range of applications including drug delivery, regenerative medicine, agriculture, and personal care products. Among the water-soluble synthetic polymers that can be processed to form hydrogels, oligo[poly(ethylene glycol) fumarate] (OPF) has attracted significant attention. The degradation of OPF can be tuned to some extent based on the poly(ethylene glycol) chain length and amount of cross-linker incorporated, but the degradation is generally quite slow, occurring over several months. Here we introduce a new approach to tune and trigger the degradation of OPF. Fumarate alkenes were functionalized to introduce protected pendent amines, that after deprotection could cyclize to 6-membered lactams, thereby cleaving the polymer backbone. Using light as a model stimulus, we demonstrated that the cleavage of an o-nitrobenzyl carbamate protecting group led to more rapid polymer degradation. Remaining unfunctionalized fumarates allowed the functionalized OPF to be cross-linked, forming a hydrogel. Treatment with light led to breakdown of the hydrogels, as indicated by a substantial reduction in the compressive modulus. The functionalization and stimulus-responsive cleavage mechanism should be applicable to other stimuli, providing a versatile approach to control OPF degradation for various applications.

Water-Soluble Synthetic Polymers: Their Environmental Emission Relevant Usage, Transport and Transformation, Persistence, and Toxicity

Water-soluble synthetic polymers (WSPs) are distinct from insoluble plastic particles, which are both critical components of synthetic polymers. In the history of human-made macromolecules, WSPs have consistently portrayed a crucial role and served as the ingredients of a variety of products (e.g., flocculants, thickeners, solubilizers, surfactants, etc.) commonly used in human society. However, the environmental exposures and risks of WSPs with different functions remain poorly understood. This paper provides a critical review of the usage, environmental fate, environmental persistence, and biological consequences of multiple types of WSPs in commercial and industrial production. Investigations have identified a wide market of applications and potential environmental threats of various types of WSPs, but we still lack the suitable assessment tools. The effects of physicochemical properties and environmental factors on the environmental distribution as well as the transport and transformation of WSPs are further summarized. Evidence regarding the degradation of WSPs, including mechanical, thermal, hydrolytic, photoinduced, and biological degradation is summarized, and their environmental persistence is discussed. The toxicity data show that some WSPs can cause adverse effects on aquatic species and microbial communities through intrinsic toxicity and physical hazards. This review may serve as a guide for environmental risk assessment to help develop a sustainable path for WSP management.

A tough conductive hydrogel with triple physical cross-linking, pH-Responsive swelling behaviors, and excellent strain sensitivity

Hydrogels as flexible strain sensors (FSSs) have attracted tremendous interest in the area of human movement monitoring. Such an application is developing rapidly. However, it is still valuable to explore hydrogel-based FSSs with excellent mechanical properties, responsiveness to stimulus, high strain sensitivity, and reliable stability. Herein, a hydrogel with triple physical cross-linking (TPC hydrogel), whose structure also included hydrophobic association-microcrystallinity-ionic coordination, was designed and fabricated. Synthetic water-soluble polymer [poly(vinyl alcohol) (PVA)] and natural polymer [sodium alginate (SA)] were introduced into the hydrogel; PVA induced microcrystal cross-linking, while SA provided ionic conductivity for the hydrogel. TPC hydrogels exhibited high toughness (5.9 MJ/m3) and excellent deformation (2490%). The introduction of SA also endowed the hydrogels with improved capability to ionize, imparting them with excellent pH-responsive swelling behavior. Impressively, TPC hydrogel-based FSSs exhibited reasonable conductivity (0.65–2.47 S/m), high sensitivity (maximum gauge factor = 10.29), and outstanding reliability and stability. This investigation broadens the avenue for the design and fabrication of hydrogels intended as FSSs with low modulus (33–45 kPa, close to human skin), excellent stretchability, and high strain sensitivity and durability.

Phosphorus-Containing Polymers as Sensitive Biocompatible Probes for 31P Magnetic Resonance

The visualization of organs and tissues using 31P magnetic resonance (MR) imaging represents an immense challenge. This is largely due to the lack of sensitive biocompatible probes required to deliver a high-intensity MR signal that can be distinguished from the natural biological background. Synthetic water-soluble phosphorus-containing polymers appear to be suitable materials for this purpose due to their adjustable chain architecture, low toxicity, and favorable pharmacokinetics. In this work, we carried out a controlled synthesis, and compared the MR properties, of several probes consisting of highly hydrophilic phosphopolymers differing in composition, structure, and molecular weight. Based on our phantom experiments, all probes with a molecular weight of ~3-400 kg·mol-1, including linear polymers based on poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC), poly(ethyl ethylenephosphate) (PEEP), and poly[bis(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)]phosphazene (PMEEEP) as well as star-shaped copolymers composed of PMPC arms grafted onto poly(amidoamine) dendrimer (PAMAM-g-PMPC) or cyclotriphosphazene-derived cores (CTP-g-PMPC), were readily detected using a 4.7 T MR scanner. The highest signal-to-noise ratio was achieved by the linear polymers PMPC (210) and PMEEEP (62) followed by the star polymers CTP-g-PMPC (56) and PAMAM-g-PMPC (44). The 31P T1 and T2 relaxation times for these phosphopolymers were also favorable, ranging between 1078 and 2368 and 30 and 171 ms, respectively. We contend that select phosphopolymers are suitable for use as sensitive 31P MR probes for biomedical applications.

Synthesis of Modified Poly(vinyl Alcohol)s and Their Degradation Using an Enzymatic Cascade.

Poly(vinyl alcohol) (PVA) is a water-soluble synthetic vinyl polymer with remarkable physical properties including thermostability and viscosity. Its biodegradability, however, is low even though a large amount of PVA is released into the environment. Established physical-chemical degradation methods for PVA have several disadvantages such as high price, low efficiency, and secondary pollution. Biodegradation of PVA by microorganisms is slow and frequently involves pyrroloquinoline quinone (PQQ)-dependent enzymes, making it expensive due to the costly cofactor and hence unattractive for industrial applications. In this study, we present a modified PVA film with improved properties as well as a PQQ-independent novel enzymatic cascade for the degradation of modified and unmodified PVA. The cascade consists of four steps catalyzed by three enzymes with in situ cofactor recycling technology making this cascade suitable for industrial applications.

Application of Electrospun Water-Soluble Synthetic Polymers for Multifunctional Air Filters and Face Masks.

The worsening of air quality is an urgent human health issue of modern society. The outbreak of COVID-19 has made the improvement of air quality even more imperative, both for the general achievement of major health gains and to reduce the critical factors in the transmission of airborne diseases. Thus, the development of solutions for the filtration of airborne pollutants is pivotal. Electrospinning has gained wide attention as an effective fabrication technique for preparing ultrafine fibers which are specifically tailored for air filtration. Nevertheless, the utilization of harmful organic solvents is the major barrier for the large-scale applicability of electrospinning. The use of water-soluble synthetic polymers has attracted increasing attention as a 'green' solution in electrospinning. We reported an overview of the last five years of the scientific literature on the use of water-soluble synthetic polymers for the fabrication of multifunctional air filters layers. Most of recent studies have focused on polyvinyl alcohol (PVA). Various modifications of electrospun polymers have been also described. The use of water-soluble synthetic polymers can contribute to the scalability of electrospinning and pave the way to innovative applications. Further studies will be required to fully harness the potentiality of these 'greener' electrospinning processes.

Water-Absorbing Bioadhesive Poly(Acrylic Acid)/Polyvinylpyrrolidone Complex Sponge for Hemostatic Agents.

Poly(acrylic acid) (PAA) is a water-soluble synthetic polymer with tissue-adhesive properties. When PAA is mixed with polyvinylpyrrolidone (PVP) in water, it forms a water-insoluble precipitate that neither swells nor adheres to tissues. We developed a novel solid/solution interface complexation method to obtain a water-swellable PAA/PVP complex. First, PAA solution was dried up in a vessel to form a film. The PAA film was then immersed in an aqueous PVP solution to obtain a highly swollen PAA/PVP hydrogel. Heat drying of the hydrogel yielded a transparent film, while freeze-drying the hydrogel provided a soft sponge. Both the PAA/PVP film and sponge could be re-swelled by water to obtain a bioadhesive gel. A relatively larger specific surface area of the sponge than that of the film led to a more rapid swelling and water absorption behavior and quick adhesion to tissues. The addition of hyaluronic acid (HA) improved the mechanical characteristics of the sponges. PAA/PVP/HA sponges had low cytotoxicity, and they exhibited high hemostatic efficiency in clinical studies after dialysis treatment or tooth extraction, even in patients on antithrombotic drugs. Such bioadhesive materials consisting of low-toxicity polymers have a high potential for use in medical hemostatic devices.

Poly(vinyl alcohol) Molecular Bottlebrushes Nucleate Ice.

Ice binding proteins (IBP) have evolved to limit the growth of ice but also to promote ice formation by ice-nucleating proteins (INPs). IBPs, which modulate these seemingly distinct processes, often have high sequence similarities, and molecular size/assembly is hypothesized to be a crucial determinant. There are only a few synthetic materials that reproduce INP function, and rational design of ice nucleators has not been achieved due to outstanding questions about the mechanisms of ice binding. Poly(vinyl alcohol) (PVA) is a water-soluble synthetic polymer well known to effectively block ice recrystallization, by binding to ice. Here, we report the synthesis of a polymeric ice nucleator, which mimics the dense assembly of IBPs, using confined ice-binding polymers in a high-molar-mass molecular bottlebrush. Poly(vinyl alcohol)-based molecular bottlebrushes with different side-chain densities were synthesized via a combination of ring-opening metathesis polymerization (ROMP) and reversible addition-fragmentation chain-transfer (RAFT) polymerization, using "grafting-to" and "grafting-through" approaches. The facile preparation of the PVA bottlebrushes was performed via selective hydrolysis of the acetate of the poly(vinyl acetate) (PVAc) side chains of the PVAc bottlebrush precursors. Ice-binding polymer side-chain density was shown to be crucial for nucleation activity, with less dense brushes resulting in colder nucleation than denser brushes. This bio-inspired approach provides a synthetic framework for probing heterogeneous ice nucleation and a route toward defined synthetic nucleators for biotechnological applications.

Structure–mechanics relationship of hybrid polyvinyl alcohol-collagen composite by molecular dynamics simulations

Polyvinyl alcohol (PVA) is a water-soluble synthetic polymer that can be used to make hydrogels for biomedical applications as well as biodegradable bags and films; however, compared to other plastics currently used for containers, it lacks mechanical strength, thermal stability, and can easily absorb water from humid environments. Although mechanical improvement has been observed by blending PVA with collagen in a hybrid hydrogel, there is a lack of fundamental understanding of the molecular mechanism, and it is not clear whether the improvement is limited to a hydrated state. Here, using classical molecular dynamics simulations based on fully atomistic models, we develop the equilibrated molecular structure of PVA with collagen and characterize its mechanics. We show that by interacting with a collagen molecule, PVA is equilibrated to a more ordered structure with each residue interacting with the near neighbors by forming more hydrogen bonds locally, making the structure stiffer than pure PVA. The structure shows higher thermal stability before melting, as well as higher rigidity in water. Our results provide the mechanism of the mechanical advantages of hybrid PVA-collagen polymer. The study demonstrates that the structure and mechanics of a synthetic polymer can be tuned by a tiny amount of a natural polymer at the molecular interface. Moreover, it may shed light on identifying a way to improve the mechanics of biodegradable polymer materials without adding much cost, which is crucial for environmental safety.Impact statementBlending natural and synthetic polymers (e.g., polyvinyl alcohol [PVA] and collagen in a hybrid hydrogel) has shown advantages in polymer mechanics, but there is a lack of fundamental understanding. Using molecular dynamics (MD) simulations based on fully atomistic models, we develop the equilibrated structure of the PVA with collagen and characterize its mechanics. We show that by interacting with a collagen molecule, PVA is equilibrated to a more ordered structure with each residue interacting with the near neighbors by forming more H-bonds locally and the structure is stiffer than pure PVA. Moreover, the structure shows a higher thermal stability before the melting point of PVA, as well as higher rigidity in water. Our results demonstrate that the structure and mechanics of a synthetic polymer can be tuned by a tiny amount of a natural polymer at the molecular interface. It provides the mechanism of the mechanical advantages as experimentally observed. This study paves the way for the multiscale modeling and mechanical design of the hybrid polymer material. It sheds light on identifying a way to improve the mechanics of biodegradable materials without adding much cost for both material functionality and environmental safety.Graphical abstract

Greener and scalable synthesis of N-methyl imines using a sustainable functional polymer

N-Methyl imines, as simple Schiff bases, could be prepared using a more sustainable and greener system, including a 33 wt.% solution of methylamine in absolute ethanol, and poly(N-vinylimidazole) (PVIm) at room temperature within 45–60 min. PVIm is a biocompatible, biodegradable and water-soluble synthetic solid functional polymer. It was indicated that PVIm can act as a reagent with multiple tasks in this reaction, including (a) reducing activation energy and stabilizing the transition states through hydrogen bond acceptor sites and low acidity of C(2)–H and (b) dehydrating activity through trapping of the released water molecules as the association phase. Inexperienced chemists can handle it easily because it is solid and less toxic than conventional catalysts – that is, piperidine, pyridine or metal- or halogen-containing salts. Additionally, ethanol and PVIm could be recycled and reused in subsequent runs without any further purification. The regenerated PVIm demonstrated stable activity after several recycle runs. No changes were detected in its chemical structure, as confirmed by Fourier transform infrared and nuclear magnetic resonance spectrum analyses.

Beyond microplastics: Water soluble synthetic polymers exert sublethal adverse effects in the freshwater cladoceran Daphnia magna

Plastic pollution is considered one of the causes of global change. However, water soluble synthetic polymers (WSSPs) have been neglected so far, although they are used in several industrial, dietary, domestic and biomedical products. Moreover, they are applied in wastewater treatment plants (WWTPs) as flocculants and coagulant agents. Hence, their presence in the aquatic environment as well as their uptake by aquatic organisms is probable, whereas no data are available regarding their potential adverse effects. Here we show in the freshwater key species D. magna exposed to five different WSSPs life history changes along with an altered level of reactive oxygen species, although acute mortality was not observed. Since daphnids act as keystone species in lake ecosystems by controlling phytoplankton biomass, even sublethal effects such as WSSPs induced changes in life history may result in cascading effects, from lower to higher trophic levels, which in turn could affect the whole food web.

Preparation of a Bioadhesive Poly(Acrylic Acid)/Polyvinylpyrrolidone Complex Gel and Its Clinical Effect on Dental Hemostasis.

Poly(acrylic acid) (PAA) is a water-soluble synthetic polymer that exhibits bioadhesive properties and has been applied in various novel medical devices, such as drug-delivery carriers and hemostatic agents. PAA forms a water-insoluble complex when mixed with polyvinylpyrrolidone (PVP). If PAA and PVP are mixed in water, they form an aggregated precipitate, which neither swells nor adheres to tissues. The formation of the hydrophobic complex was caused by hydrophobic interactions between the main chains of both polymers aligned the same as a zipper. To hinder the zipper-like alignment of the polymer main chains, hyaluronic acid (HA), a macromolecular viscous polysaccharide, was added to the PVP solution prior to complex formation. When the initial concentration of PAA was lower than 0.05%, HA effectively prevented the aggregation of PAA/PVP complexes and resulted in a slightly clouded suspension. Freeze-drying of the mixture yielded a soft white sponge, which could immediately swell in water to form a highly bioadhesive hydrogel. The PAA/PVP complex prepared with HA exhibited high hemostatic efficiency in clinical studies, even in patients on antithrombotic drugs.

Water-soluble fluorescent supramolecular polymer network with sustainable “Fluorescence on” based on AIEgen-containing host-guest interactions

Inspired by miraculous bioluminescence phenomena, many synthetic water-soluble fluorescent supramolecular polymer networks (WFSPNs) have attracted wide attention. Up to now, WFSPNs could be divided into two categories on a basis of aggregation-caused quenching (ACQ) effect or aggregation-induced emission (AIE) effect, respectively. However, these two kinds of WFSPNs could only be emissive at partial crosslinking degrees. Herein, we constructed WFSPNs with sustainable “fluorescence on” property. Firstly, cyanostilbene molecule ZPP with AIE property and cyanostilbene-based polymer 4APEG-ZPP were synthesized. Then γ-CD was added into the aqueous solution of 4APEG-ZPP to self-assemble into WFSPNs. This self-assembled process was based on host-guest interactions driven by the hydrophobic interactions. Upon adding γ-CD into the aqueous solution of 4APEG-ZPP, yellow fluorescence was emitted on account of cyanostilbene groups in 4APEG-ZPP tending to form a “dimer” through intermolecular interactions, like π-π stacking and CN∙∙∙π. Moreover, green fluorescence emitted by WFSPNs could be seen with the larger amount of γ-CD being mixed into the 4APEG-ZPP aqueous solution on account of the increase of crosslinking degrees. Obviously, the fluorescence wassustainable with the concentration of γ-CD increasing. Therefore, this system realized the sustainable “fluorescence on” property during the transformation from polymers to networks.

Photocatalysis and flocculation processes for recycling aquaculture effluent into nutrient-rich irrigation water

Abstract This research aimed to create a novel technique for recovering fertilizers from aquaculture effluent to overcome potential non-renewable fertilizers shortages. There are two steps: a photocatalyst technique for nutrient mobilization, succeeded by solids precipitating with two natural and one synthetic flocculants. The photocatalytic degradation of organonitrogen compounds in batch experiments started under the irradiation of sunlight. Following that, photocatalytic breakdown of organonitrogen compounds produces inorganic nitrogen constituents like NH4+, NO2−, and NO3−, which could be used as manure. It was found that, after 12 h of circulation, the concentration of inorganic nitrogen became NH4+ = 17.2 g/L, NO2− = 18.1 mg/L, and NO3− = 15.9 mg/L. The jar test was adopted to assess the capacity of two natural compounds (tamarind kernel polysaccharide (TKP) and tannin-based substance (TBS)) and synthetic water-soluble polymer cationic polyacrylamide (SWP) to reduce turbidity, total suspended solids (TSS), chemical oxygen demand (COD) and colour. The findings revealed that with a dose of 20 mg/L of TBS, 20 mg/L of TKP, and 50 mg/L of SWP, the maximum turbidity reductions were 95, 93, and 94%, respectively. The TBS was slightly better than TKP and much better than SWP in terms of coagulation activities with TSS, COD and colour maximum removal efficiencies.

Identification of Water-Soluble Polymers through Discrimination of Multiple Optical Signals from a Single Peptide Sensor.

The pollution of water environments is a worldwide concern. Not only marine pollution by plastic litter, including microplastics, but also the spillage of water-soluble synthetic polymers in wastewater have recently gained increasing attention due to their potential risks to soil and water environments. However, conventional methods to identify polymers dissolved in water are laborious and time-consuming. Here, we propose a simple approach to identify synthetic polymers dissolved in water using a peptide-based molecular sensor with a fluorophore unit. Supervised machine learning of multiple fluorescence signals from the sensor, which specifically or nonspecifically interacted with the polymers, was applied for polymer classification as a proof of principle demonstration. Aqueous solutions containing different polymers or multiple polymer species with different mixture ratios were identified successfully. We found that fluorophore-introduced biomolecular sensors have great potential to provide discriminative information regarding water-soluble polymers. Our approach based on the discrimination of multiple optical signals of water-soluble polymers from peptide-based molecular sensors through machine learning will be applicable to next-generation sensing systems for polymers in wastewater or natural environments.