Macromolecular Organic Compounds Research Articles

Bioaugmentation Technology for Treatment of Toxic and Refractory Organic Waste Water Based on Artificial Intelligence.

With the development of modern chemical synthesis technology, toxic and harmful compounds increase sharply. In order to improve the removal efficiency of refractory organic matter in waste water, the method of adding powdered activated carbon (PAC) to the system for adsorption was adopted. Through the analysis of organic matter removal rule before and after waste water treatment, it can be found that PAC is easy to adsorb hydrophobic organic matter, while activated sludge is easy to remove hydrophilic and weakly hydrophobic neutral organic matter. Powdered activated carbon-activated sludge SBR system (PAC-AS) system is obviously superior to AS and PAC system in removing organic matter of hydrophilic and hydrophobic components, that is, biodegradation and PAC adsorption are additive. Compared with the control system, the Chemical Oxygen Demand (COD) removal rate of refractory substances increased by 8.36%, and PAC had a good adsorption effect on small molecular weight organic compounds, but with the increase of molecular weight of organic compounds, the adsorption effect of PAC gradually weakened, and it had no adsorption effect on macromolecular organic compounds. Based on the research of fuzzy control theory, an Agent control system for ozone oxidation process of industrial waste water based on Mobile Agent Server (MAS) theory was established, which was realized by fuzzy control method. The simulation results showed strong stability and verified the feasibility and adaptability of the distributed intelligent waste water treatment system based on MAS theory in the actual control process.

The characteristic of N-nitrosodimethylamine precursor release from algal organic matter and degradation performance of UV/H2O2/O3 technology

Seasonal cyanobacterial blooms in eutrophic water releases algal organic matter (AOM), which contains large amount of dissolved organic nitrogen (DON) and is difficult to be removed effectively by conventional treatment processes (e.g., coagulation and sand filtration) because of its high hydrophilicity. Moreover, N-nitrosodimethylamine (NDMA) can be generated by the reaction of AOM with disinfectants in the subsequent disinfection process. In this study, the formation of NDMA from different AOM components was explored and the control of algal-derived NDMA precursors by UV/H2O2/O3 was evaluated. The results showed that the hydrophilic and polar components of AOM with the low molecular weight had higher NDMA yields. UV-based advanced oxidation process (AOPs) is effective in degrading NDMA precursors, while the removal rate can be affected greatly by UV doses. The removal rate of NDMA precursors by UV/H2O2/O3 is higher than by UV/H2O2 or UV/O3 which can reach 95% at the UV dose of 400 mJ/cm2. An alkaline environment reduces the oxidation efficiency of UV/H2O2/O3 technology, while an acidic environment is conducive to its function. Inorganic anions such as HCO3−, SO42−, Cl− and NO3− are potential to compete with target algal-derived NDMA precursors for the oxidants reaction and inhibit the degradation/removal of these precursors. The degradation of algal-derived NDMA precursors by UV/H2O2/O3 is mainly accomplished by the oxidation of DON with secondary amide groups, and the main degradation mechanism by UV/H2O2/O3 was through the initial decomposition of macromolecular organic compounds such as biopolymers and humic substances and the further degradation of resulting small molecular components.

Understanding the abiotic interaction between phosphate and macromolecular organic compounds in waste activated sludge during anaerobic treatment

The abiotic interaction between ferric phosphate and major macromolecular organics (protein, saccharide, humic substance) in waste activated sludge (WAS) were studied, and the effect of phosphate on protein and the reaction mechanism were discussed in particular. With the addition of ferric phosphate, the concentration of protein was greatly reduced with a removal efficiency of 77.3%, accompanied by a remarkable increment of NH4+-N concentration (13.5 mg/L) when the release efficiency of NH4+-N reached 52.7%, while fulvic acid (FA) and glucose barely changed. PO43‐ was the functional ion dominating the protein decomposition and NH4+-N release. The maximal release efficiency of NH4+-N (66.9%) occurred at pH 7, and the NH4+-N concentration mainly depended on the protein concentration, while the presence of FA and glucose would interfere the decomposition of protein. The analytical results of circular dichroism (CD) suggested that the reaction went through two stages: firstly, the process was relatively stable and phosphate showed a tendency to facilitate the transition from helices to β-sheets; then peptide chains on the helices were broken and deamination of amino acid residues occurred. Due to the loss of hydrophilic groups, hydrophobicity of the residue was further enhanced, resulting in its co-precipitation with protein. The results are applicable to proteins with similar structures to bovine serum albumin (BSA). This study provides a novel insight into the transformation of organic matters and phosphorus (P) in the anaerobic treatments of WAS.

Design of facile technology for the efficient removal of hydroxypropyl guar gum from fracturing fluid.

With the increasing demand for energy, fracturing technology is widely used in oilfield operations over the last decades. Typically, fracturing fluids contain various additives such as cross linkers, thickeners and proppants, and so forth, which makes it possess the properties of considerably complicated components and difficult processing procedure. There are still some difficult points needing to be explored and resolved in the hydroxypropyl guar gum (HPG) removal process, e.g., high viscosity and removal of macromolecular organic compounds. Our works provided a facile and economical HPG removal technology for fracturing fluids by designing a series of processes including gel-breaking, coagulation and precipitation according to the diffusion double layer theory. After this treatment process, the fracturing fluid can meet the requirements of reinjection, and the whole process was environment friendly without secondary pollution characteristics. In this work, the fracturing fluid were characterized by scanning electron microscopy (SEM), Energy dispersive X-ray (EDX), X-ray diffraction (XRD) and Fourier transformed infrared (FTIR) spectroscopy technologies, etc. Further, the micro-stabilization and destabilization mechanisms of HPG in fracturing fluid were carefully investigated. This study maybe opens up new perspective for HPG removal technologies, exhibiting a low cost and strong applicability in both fundamental research and practical applications.

Brush Layer Charge Characteristics of a Biomimetic Polyelectrolyte-Modified Nanoparticle Surface.

Nanoparticle surface charge regulation technology plays an important role in ion rectification, drug delivery, and cell biology. The biomimetic polyelectrolyte can be combined with nanoparticles by nanomodification technology to form a layer of coating, which is called the brush layer of nanoparticles. In this study, based on the Poisson-Nernst-Planck (PNP) equation system, a theoretical model considering a bionic electrolyte brush layer with charge density regulated by a chemical reaction is constructed. The charge properties of brushed nanoparticles are studied by changing the sizes of nanoparticles, the pH value of the solution, background salt solution concentration, and brush layer thickness. The result shows that the charge density of brushed nanoparticles increases with the increase of particle size. The isoelectric point (IEP) of the equilibrium reaction against the brush layer is pH = 5.5. When the pH < 5.5, the charge density of the particle brush layers decreases with the increase of pH, and when the pH > 5.5, the charge density of the particle brush layer increases with the increase of pH. By comparing the charge density of different brush thicknesses, it is found that the larger the brush thickness, the smaller the charge density of the brush layer. This research provides theoretical support for the change of the through pore velocity when macromolecular organic compounds pass through nanopores.

New Illumination and Temperature Constraints of Mercury's Volatile Polar Deposits.

Images from the Mercury Dual Imaging System (MDIS) aboard the MErcury Surface, Space ENvironment, GEochemistry, and Ranging mission reveal low-reflectance polar deposits that are interpreted to be lag deposits of organic-rich, volatile material. Interpretation of these highest-resolution images of Mercury’s polar deposits has been limited by the available topography models, so local high-resolution (125 m pixel−1) digital elevation models (DEMs) were made using a combination of data from the Mercury Laser Altimeter (MLA) and from shape-from-shading techniques using MDIS images. Local DEMs were made for eight of Mercury’s north polar craters; these DEMs were then used to create high-resolution simulated image, illumination, and thermal models. The simulated images reveal that the pixel brightness variations imaged within Mercury’s low-reflectance deposits are consistent with scattered light reflecting off of topography and do not need to be explained by volatile compositional differences as previously suggested. The illumination and thermal models show that these low-reflectance polar deposits extend beyond the permanently shadowed region, more than 1.0 km in some locations, and correspond to a maximum surface temperature of greater than 250 K but less than 350 K. The low-reflectance boundaries of all eight polar deposits studied here show a close correspondence with the surface stability boundary of coronene (C24H12). While coronene should only be viewed as a proxy for the myriad volatile compounds that may exist in Mercury’s polar deposits, coronene’s surface stability boundary supports the idea that Mercury’s low-reflectance polar deposits are composed of macromolecular organic compounds, consistent with the hypotheses of exogenous transport and in situ production.

PLASTIC POLLUTION IS ONE OF THE MAIN ENVIRONMENTAL PROBLEM OF HUMANITY

Тhe article is devoted to the global environmental problem of plastic waste pollution. Now, about 9 billion tons of primary plastic have been produced. Of this amount, 6.3 billion tons is plastic waste, of which 9 % was recycled, 12 % incinerated, and 79 % accumulated in landfills or in the environment. The main feature of plastic materials is their stability. Once in the environment as waste, plastic can be in its original state for more than 450 years. The purpose of the article is to study the current state of production and use of plastics, as well as the field of plastic waste management; identification of perspective methods for solving the problem of plastic pollution. Plastics are organic macromolecular compounds that have high quality characteristics. Due to this, they became widespread. There are different types of plastics: thermoplastics, thermosets, foams and bioplastics. Currently, 40% of plastic is used once, after which it is discarded. Under the influence of various factors in the environment plastic slowly breaks down into small fragments, known as microplastics. Microplastic particles get into the soil, water, and through food chains can enter the human body. Potentially microplastics can negatively affect the human body. To solve the problem of accumulation of plastic waste in the environment, many countries around the world, including Ukraine, are implementing a waste management system based on the European waste management hierarchy. The hierarchy reflects five approaches to waste management: Removal (waste disposal and incineration without energy production), Recovery (waste incineration with energy production), Recycling (waste conversion into secondary raw materials for reuse), Reuse (waste reuse without recycling) and Prevention (waste amount minimization). Disposal is the least efficient way of waste management, and recycling and prevention are the most effective ways. Keywords: plastic, waste, pollution, environment, landfill, recycling.

Impact of monovalent cations on the separation performance of graphene oxide membrane for different organic matters.

Graphene oxide (GO) membrane has become a promising membrane due to its advantages of high flux, good anti-pollution performance, and controllable cost. Since wastewater contains inorganic ions and organic substances, the effect of inorganic ions on the removal of organic matters has attracted attention. This study investigated the impact of monovalent cations (Na+ and K+) on the removal of different organic matters by GO membranes. The results showed that the removal by GO membranes of both macromolecular organic compounds (humic acid, sodium alginate, and bull serum albumin) and small molecular organic substances (new coccine, methyl orange, and methylene blue) were high (>75%). The coexisting Na+ caused the increase in flux and the decrease in removal of small molecular organic matters, while the impact on the removal of macromolecular organic matters was weak. The impact of the coexisting K+ was weaker than Na+. With the crosslinking of ethylenediamine, the structure of GO membrane was more stable. The impacts of Na+ on the flux and separation performance of crosslinked membranes were less than that of non-crosslinked membranes. This suggests that crosslinked GO membrane has more potential for practical wastewater treatment.

Treatment of Produced Water with Photocatalysis: Recent Advances, Affecting Factors and Future Research Prospects

Produced water is the largest byproduct of oil and gas production. Due to the complexity of produced water, especially dissolved petroleum hydrocarbons and high salinity, efficient water treatment technologies are required prior to beneficial use of such waste streams. Photocatalysis has been demonstrated to be effective at degrading recalcitrant organic contaminants, however, there is limited understanding about its application to treating produced water that has a complex and highly variable water composition. Therefore, the determination of the appropriate photocatalysis technique and the operating parameters are critical to achieve the maximum removal of recalcitrant compounds at the lowest cost. The objective of this review is to examine the feasibility of photocatalysis-involved treatment for the removal of contaminants in produced water. Recent studies revealed that photocatalysis was effective at decomposing recalcitrant organic compounds but not for mineralization. The factors affecting decontamination and strategies to improve photocatalysis efficiency are discussed. Further, recent developments and future research prospects on photocatalysis-derived systems for produced water treatment are addressed. Photocatalysis is proposed to be combined with other treatment processes, such as biological treatments, to partially reduce total organic carbon, break down macromolecular organic compounds, increase biodegradability, and reduce the toxicity of produced water.

Competition between fulvic acid and phosphate-mediated surface properties and transport of titanium dioxide nanoparticles in sand porous media

Fulvic acid (FA) is a series of organic macromolecular compounds with many oxygen-containing functional groups and is easy to complex with nanoparticles (NPs) in the environment, thus affecting the stability and mobility of NPs in the water environment. Therefore, it is necessary to investigate the transport behavior of nano titanium dioxide (nTiO2) particles with FA in the presence of phosphate (P). A series of transport experiments were conducted by using nTiO2 suspended in phosphate background electrolyte with and without the addition of FA passing through water-saturated sand columns. The zeta potentials, hydrodynamic radii, and aggregation kinetics were measured, and the extended Derjaguin-Landau-Verwey-Overbeek (DLVO) theory and two-site kinetic attachment model (TSKAM) were employed to explain the underlying mechanism. The experimental results showed that the presence of FA compressed the transport of nTiO2 in phosphate electrolyte due to formation of larger complex via the adsorption of organic FA molecules onto nTiO2, which can strongly compete with phosphate adsorption, leading to reduced electrostatic repulsive forces between nTiO2 and sand. In the absence of FA at low pH (6.0), transport of individual nTiO2 was increased by low phosphate adsorption in response to increased phosphate levels, and then, transport was decreased with the increased number of cations (Na+) from the phosphate (P ≥ 1.0 mM) electrolyte due to the compressed electric double layer. From the goodness-of-fit of the modeling results, the TSKAM provided a good prediction for the retention and transport of nTiO2 in the copresence of FA and phosphate. The compressed transport of nTiO2 in the copresence of FA and phosphate was distinct from the synergistic transport in the copresence of humic acid.

Ancestry and adaptive radiation of Bacteroidetes as assessed by comparative genomics

To date, the phylum Bacteroidetes comprises more than 1,500 described species with diverse ecological roles. However, there is little understanding of archetypal Bacteroidetes traits at a genomic level. In this study, a representative set of 89 Bacteroidetes genomes was compiled, and pairwise reciprocal best-match gene comparisons and gene syntenies were used to identify common traits that allowed Bacteroidetes evolution and adaptive radiation to be traced. The type IX secretion system (T9SS) was highly conserved among all studied Bacteroidetes. Class-level comparisons furthermore suggested that the ACIII-caa3COX super-complex evolved in the ancestral aerobic bacteroidetal lineage, and was secondarily lost in extant anaerobic Bacteroidetes. Another Bacteroidetes-specific respiratory chain adaptation was the sodium-pumping Nqr complex I that replaced the ancestral proton-pumping complex I in marine species. T9SS plays a role in gliding motility and the acquisition of complex macro-molecular organic compounds, and the ACIII-caa3COX super-complex allows effective control of electron flux during respiration. This combination likely provided ancestral Bacteroidetes with a decisive competitive advantage to effectively scavenge, uptake and degrade complex organic molecules, and therefore has played a pivotal role in the successful adaptive radiation of the phylum.

Additives synergy for stable interface formation on rechargeable lithium metal anodes

The attention towards lithium (Li) metal anodes has been rekindled in recent years as it would boost the energy-density of Li batteries. However, notorious safety issues and cycling instability severely hinder their commercialization, especially when cycled in traditional carbonic ester electrolytes that exhibit a wide voltage window and are compatible with most of the cathode materials. Herein, lithium difluorophosphate (LiDFP) and vinylene carbonate (VC) are combined, and demonstrated to be synergistic in constructing in situ a mechanically stable and highly Li-ion conducting surface film on the Li metal anode. This results in uniform and compact Li deposition largely suppressing the formation of Li dendrites, dead lithium and irreversible Li-species as revealed by operando neutron depth profiling (NDP). This enables long-term cycling stability and enhancement of the Coulombic efficiency for rechargeable Li metal anodes. By combining solid state nuclear magnetic resonance (SSNMR) and spectroscopic studies, it is demonstrated that VC slows down the LiDFP reduction, yet promoting the breaking of the P–F bonds, which leads to a protective film. This film is rich in LiF–Li3PO4 inorganic compounds, distributed homogeneously, that is embedded in a matrix of P–O–C species and macromolecular organic compounds like lithium ethylene dicarbonate. This composition is responsible for the improved ionic conductivity and mechanical stability of the protective film during extended cycles. The detailed insight in the additives interaction provides new opportunities for the design of rational surface films necessary for realizing high-performance lithium metal batteries.

Spectral study of humic substance extract from pressurized oxidizing slag of Carlin-typed gold deposit

Carbonaceous matters in Carlin-type gold deposit, especially the humic substance, which have a serious preg-robbing effect on the process of cyanidation. In this paper, the humic acid and fulvic acid were extracted from oxidizing slag via pre-activation alkaline-heat method, and using FTIR and UV-Vis spectra to study the molecular structure of humic acid extract and fulvic acid extract. The FITR spectrum demonstrated that hydroxyl, carboxyl and benzene rings characteristic stretching vibration peaks occurred in spectra of humic acid and fulvic acid, but humic acid extract had a finer molecular structure. The result of UV-Vis spectra analysis showed that the extract contained alkyl-substituted benzene ring structure, and the amount of carboxyl groups and hydroxyl groups in fulvic acid molecule was larger than that of humic acid. The fulvic acid extract contained more chromophores, while humic acid molecules have a higher degree of humification and a higher average molecular weight. Although there were some differences in the molecular structure of the both, they were both complex macromolecular organic compounds with a benzene ring as a basic unit.

Adsorption and fractionation of Pt, Pd and Rh onto inorganic microparticles and the effects of macromolecular organic compounds in seawater

Adsorption and fractionation of Pt, Pd and Rh (defined here as platinum group elements, PGEs) onto the representative inorganic microparticles, including Fe2O3, MnO2, CaCO3, SiO2, Al2O3 and kaolinite in seawater were investigated. The effects of macromolecular organic compounds (MOCs) as the representatives of organic matter, including humic acids (HA), bovine serum albumin (BSA) and carrageenan, on the adsorption were also studied considering that organic matter is ubiquitous in seawater and indispensable to marine biogeochemical cycles. In the absence of MOCs, the representative mineral particles Fe2O3 and MnO2 had the strongest interaction with PGEs. The adsorption of PGEs onto the representative biogenic particles SiO2 and CaCO3 and lithogenic particles Al2O3 and kaolinite was similar or weaker than onto the mineral particles. MOCs inhibited the interaction between PGEs and the particles except for Pt and Pd onto the biogenic particles in artificial seawater. This impediment may be closely related to the interaction between particles, MOCs and elements. The partition coefficient (log Kd) of Pt was similar (∼4.0) in the presence of MOCs, indicating that the complexation between Pt and MOCs was less important than hydrolysis or adsorption onto the acid oxide particle surface. Rh tended to fractionate onto the mineral and lithogenic particles in the presence of HA and carrageenan, while Pd was more likely to fractionate onto the biogenic particles. However, BSA enhanced the fractionation tendency of Pd onto the mineral particles. The results indicate that the adsorption behavior of Pd onto inorganic particles was significantly affected by the composition or the type of MOCs. Hence, the interaction between PGEs and inorganic particles may be greatly affected by the macromolecular organic matter in the ocean.

Adsorption kinetics of platinum group elements onto macromolecular organic matter in seawater

Adsorption kinetics of the interaction between Pt, Pd and Rh (defined here as platinum group elements, PGEs) ions and macromolecular organic compounds (MOCs, >10 kDa), including humic acid, carrageenan and bovine serum albumin, and different cutoff fractions of natural organic matter (>1 kDa and >3 kDa) obtained from seawater using centrifugal ultrafiltration devices were investigated. For a given element, all the adsorption kinetics did not reach equilibrium except the interaction between Pt and >1 kDa cutoff, and between Pd and humic acid. For all the tested MOCs, the adsorption kinetics could be divided into two stages, a rapid adsorption process in the first 8 h and the desorption stage after the first 8 h until the equilibrium. The change trend of partition coefficient (log10Kd) values with experiment time was consistent with that of the kinetic curves. However, in the interaction between PGE ions and natural dissolved organic matter (NDOM), an obvious difference in the change trends of log10Kd and kinetic curves was observed. It indicated that the partition behavior of PGE ions interacting with NDOM in seawater was a combined effect of different organic constituents. The adsorption and log10Kd of PGEs in the >1 kDa NDOM fraction were higher and more stable than those in the >3 kDa NDOM fraction. The results also indicated that the 1–3 kDa NDOM may dominate the interaction between PGEs ions and NDOM. Moreover, no kinetic model could perfectly simulate the adsorption process. It indicated that the colloidal struction and morphology of MOCs or NDOM in seawater might be inhomogeneous. Hence, the interaction between PGE ions and organic matter in seawater was a complicated process and needs further research.

Transformation of organic substances in the conjugate series of surface waters of North Karelia

In this study, compositions of organic matter were investigated in the conjugate series of natural waters, including that from soil water, wetlands, streams, and lakes. In determinations of compositions of aliphatic and benzoic acids and humic substances, humic substances comprised the bulk of dissolved organic carbon, with 28% in lake waters and 57% in waters of wetlands and a weighted average molecular mass of 1 kDa. Aliphatic and benzoic acids comprised ≤ 2% of the total carbon content of water-soluble organic compounds. Transformations of dissolved organic matter occurred in a series of surveyed waters. Specifically, compositions and specific characteristics are dynamic, and increases in the fraction with a molecular weight of &lt; 1 kDa were associated with photo- and bio-degradation of macromolecular organic compounds.

Purification of aqueous media from toxicants carbon-mineral sorbent

To purify aquatic environments from various toxicants, we obtained a carbon-mineral sorbent from the reed stems of the South (Phragmitesaustralis) by carbonization. At the stage of carbonization of the crushed reed, a carcass, containing carbon and silicate constituents, is formed. Depending on the type of feedstock and the carbonization temperature of the organic component, the content of the silicate component varies in the range of 20-30%. The process is carried out until a sorbent containing 70-80% of the carbon component, 29-19% of the silicate component and 1% of water is obtained. The adsorption capacity of the obtained carbon-mineral sorbent towards to medium and macromolecular organic compounds, and heavy metals was studied. As a result, it was established that the carbon-mineral sorbent obtained from the reed stems of the South (Phragmitesaustralis) has moderately distributed sizes of macro- and micropores. The presence of two constituents, carbon and silicate, in the structure of the obtained sorbent promotes the sorption of phenols, hydrocarbons, barbiturates, cholesterol derivatives, aminoglycosides, anthracyclines and other compounds, as well as ions of heavy metals, which makes it possible to use a sorbent in the chemical industry for purification of sewage, natural waters and it can be proposed for the purification of biological fluids.

Behavior and Degradation of Polycyclic Aromatic Hydrocarbons (PAHs) in Coking Wastewater of A/O2 and A/O/H/O Processes

Polycyclic aromatic hydrocarbons (PAHs) are typical organic pollutants found in coking wastewater, and their behavior and reduction can be affected by different treatment processes. Based on these considerations, this study investigated the behaviors of PAHs in coking wastewater under A/O2 and A/O/H/O treatment processes, respectively. In order to evaluate variations in PAH removal under two different treatment processes, samples were taken from different treatment units for quantification of PAHs using gas chromatography-mass spectrometry. Results showed that PAHs were barely degraded in anaerobic tanks of either treatment process and accumulated much higher concentrations than in aerobic and hydrolytic tanks. While low molecular weight PAHs (LMW PAHs) in aqueous phase from anaerobic tanks were degraded effectively in aerobic tanks, high molecular weight PAHs (HMW PAHs) mostly accumulated in the sludge phase; these potentially pose a higher environmental risk and therefore need to be treated separately. Moreover, the A/O/H/O process showed higher degradation of PAHs bioavailability and higher removal effectiveness for PAHs with four or more benzene rings than the A/O2 process; this is attributed to the hydrolytic tank's ability to promote hydrolysis of macromolecular organic compounds and therefore improve biodegradability of PAHs. Comprehensive results from the study indicated that the A/O/H/O process is more advantageous for degradation of PAHs than the A/O2 process.

Macromolecular organic compounds from the depths of Enceladus.

Saturn’s moon Enceladus harbours a global ocean1, which lies under an ice crust and above a rocky core2. Through warm cracks in the crust3 a cryo-volcanic plume ejects ice grains and vapour into space4–7, providing access to materials originating from the ocean8,9. Hydrothermal activity is suspected to be occurring deep inside the water-percolated porous core10–12, powered by tidal dissipation13. So far only simple organic compounds with molecular masses mostly below 50u have been observed in the plume6,14,15. Here we report observations of emitted ice grains containing concentrated, complex, macromolecular organic material with molecular masses above 200u. The data provides key constraints on the macromolecular structure and is suggestive of a thin organic-rich film on top of the oceanic water table. There, organic nucleation cores generated by bubble bursting allow probing of Enceladus’ organic inventory in drastically enhanced concentrations.

Gas Sensors Based on Molecular Imprinting Technology

Molecular imprinting technology (MIT); often described as a method of designing a material to remember a target molecular structure (template); is a technique for the creation of molecularly imprinted polymers (MIPs) with custom-made binding sites complementary to the target molecules in shape; size and functional groups. MIT has been successfully applied to analyze; separate and detect macromolecular organic compounds. Furthermore; it has been increasingly applied in assays of biological macromolecules. Owing to its unique features of structure specificity; predictability; recognition and universal application; there has been exploration of the possible application of MIPs in the field of highly selective gas sensors. In this present study; we outline the recent advances in gas sensors based on MIT; classify and introduce the existing molecularly imprinted gas sensors; summarize their advantages and disadvantages; and analyze further research directions.