Water Stability Research Articles

Research on deicing performance and environmental impact of anti-freezing asphalt mixtures

Snow and ice on pavement surface can cause a significant safety concern for drivers. This research investigates the deicing performance of the asphalt mixtures containing a self-prepared salt-storage additive (SSA), as well as their environmental impacts. A pull-off test was developed to evaluate the adhesion between the ice layer and asphalt mixture surface. The self-prepared SSA was incorporated into the asphalt mixtures by replacing mineral filler at percentages of 0 %, 20 %, 50 %, and 100 % by volume. The influence of self-prepared SSA on the pavement performance of asphalt mixtures was firstly investigated in this study, including the high-temperature stability, low-temperature performance, and water stability. The deicing performance of the asphalt mixtures containing self-prepared SSA and commercial product was determined by using the freezing point tests, ice-melting tests, and self-designed pull-off tests. To evaluate the environmental impacts of those anti-freezing asphalt mixtures, corrosion tests and seed germination tests were also employed in this study. Testing results showed that the addition of self-prepared SSA compromised the pavement performance of asphalt mixtures, but all measured properties met the specified requirements. The self-prepared SSA can effectively reduce the freezing point of the asphalt mixtures and shorten the ice melting time by 30 %, which has a similar or even better deicing effect as compared to the commercial salt-storage additive. Notably, the pull-off tests showed that the self-prepared SSA can significantly reduce the adhesion force between ice layer and asphalt mixture surface. The environmental impacts of asphalt mixtures containing self-prepared SSA were found to be within a reasonable range.

Fabrication of polysaccharide-coated oleanolic acid-curcumin-coassembled nanoparticles (OA/Cur NPs): Enhancement of colloidal stability and water solubility

Natural terpenoid carriers, such as oleanolic acid (OA), can enhance the water solubility and stability of hydrophobic compounds such as curcumin (Cur). However, improving the colloidal stability of nanoparticle emulsions and resolving the redispersion problem of freeze-dried nanoparticle powders remain significant challenges. In this study, we fabricated coassembled oleanolic acid-curcumin nanoparticles (OA/Cur NPs) and applied a polysaccharide surface coating method to improve their colloidal stability and water solubility. The results showed that the optimal ratio of Cur/OA for preparing OA/Cur NPs was 4:10, resulting in a high encapsulation efficiency (EE) of Cur (75.2%). Additionally, TEM, contact angle tests, Turbiscan TOWER optical stability analysis of the polysaccharide-coated OA/Cur NP emulsions and redispersion tests of their lyophilized powders verified the advantages of carboxymethyl chitosan/β-cyclodextrin (CMC/β-CD) coating over other polysaccharides. This study indicated that polysaccharide coating is an effective method for enhancing the colloidal stability, water solubility, and redispersibility of OA/Cur NPs.

Safety of Tap Water in Terms of Changes in Physical, Chemical, and Biological Stability

Monitoring the quality of tap water in the distribution system and the ability to estimate the risk of losing its sanitary safety is an important aspect of managing the collective water supply system. During monitoring, the physical, chemical, and biological stability of water was assessed, which is the main determinant ensuring the appropriate quality of water for consumers. The physicochemical and microbiological quality of water was analyzed for two distribution systems (DSs), including the analysis of heavy metals (Zn, Fe, Mn, Cr, Ni, Cu, Cd, Pb). The tests carried out showed that in both distribution systems, the water supplied to consumers met the guidelines for water intended for human consumption. It can be considered that the risk of uncontrolled changes in water quality in DSs with an average water production of <10,000 m3/d and the length of water pipelines < 150 km is very low. The water introduced into the system differed in the place of water intake and water purification technology, which influenced the final water quality. In DS(II), higher values were recorded for hardness, conductivity, calcium, alkalinity, nitrates, and DOC. It was found that the content of heavy metals during water transport to the consumer increased in the case of DS(I) for Zn, Ni, Cu, Cd, and Pb, and in the case of DS(II) for Fe, Mn, Ni, Cu, Cd, and Pb. The observed differences resulted from the different quality of the intake water as well as from different materials used to build internal installations and their age and technical condition. The analyzed tap water was characterized by physical and chemical stability. However, the water did not meet the guidelines for water biostability due to the increased content of biogenic substances.

Electrochemical Surface Nanostructuring of Ti47Cu38Fe2.5Zr7.5Sn2Si1Ag2 Metallic Glass for Improved Pitting Corrosion Resistance

Ti‐based bulk metallic glasses are envisioned for human implant applications. Yet, while their elevated Cu content is essential for a high glass‐forming ability, it poses biocompatibility issues, necessitating a reduction in near‐surface regions. To address this, surface treatments that simultaneously generate protective and bioactive states, based on nanostructured Ti and Zr‐oxide layers are proposed. An electrochemical pseudo‐dealloying process using the bulk glass‐forming Ti47Cu38Fe2.5Zr7.5Sn2Si1Ag2 alloy is defined. Melt‐spun ribbons are immersed in hot concentrated nitric acid solution, monitoring the anodic polarization behavior. From the current density transient measurements, together with surface studies (field‐emission scanning electron microscopy, transmission electron microscopy, and Auger electron spectroscopy), the surface reactions are described. This nanostructuring process is divided into three stages: passivation, Cu dissolution, and slow oxide growth, leading to homogenous nanoporous and ligament structures. By tuning the applied potential, the pore and ligament sizes, and thickness values are adjusted. According to X‐ray photoelectron spectroscopy, these nanoporous structures are Ti and Zr‐oxides rich in hydrous and nonhydrous states. In a simulated physiological solution, for those treated glassy alloy samples, complete suppression of chloride‐induced pitting corrosion in the anodic regime of water stability is achieved. This high corrosion resistance is similar to that of clinically used cp‐Ti.

Gelatin nanocarriers assembled by a self-immolative cross-linker for targeted cancer therapy

With a number of outstanding properties, gelatin is an ideal candidate for assembling nanoplatforms in biomedical applications. Generally, gelatin nanocarriers are cross-linked by aldehydes to improve their stability in water solution. However, aldehydes could cause multiple toxicities and their cross-linking products are uncontrollable. Here, we first used a self-immolative cross-linker to assemble gelatin nanocarriers for the controlled release of drugs and targeted cancer therapy. The cross-linker contains a disulphide bridge and two symmetrical succinimidyl-esters, endowing it with multiple functions: 1) to cross-link the gelatin nanocarriers and thus improve their stability in water; 2) to conjugate the drug and tumor-targeting ligands with nanocarriers through covalent linkage; 3) to redox-responsively degrade the nanocarriers through hydrolysis of disulphide bridge; and 4) to produce traceless drug molecules through self-immolative reaction. Good biocompatibility and controllable drug release were demonstrated by in vitro experiments. Both qualitative and quantitative analyses confirmed the intracellular uptake of the nanocarriers by using doxorubicin (DOX) as a drug model and phenylboronic acid (PBA) as the targeting ligand. In vivo results demonstrated high therapeutic efficiency and low toxic side effects of the DOX loaded nanocarriers against artificial liver tumors.

Preparation of Conductive Asphalt Concrete Based on the Action Mechanism of Conductive Phase Materials

Carbon fiber powder (CFP) was first applied to conductive asphalt concrete as a conductive phase material, but its action mechanism has not been clarified. In this paper, atomic force microscopy (AFM) and molecular dynamics (MDs) simulation are used to study the carbon fiber powder mechanism of action, guide the preparation of conductive asphalt concrete, and study the electrothermal properties of conductive asphalt concrete. The results show that carbon fiber powder weakens the adhesion property of asphalt mastic, and this weakening further strengthens in the water–temperature coupling, so water stability and conductivity are used as evaluation indicators to determine that the optimal content of carbon fiber powder is 2.0% and that the optimal content of carbon fibers (CFs) is 0.4%. Carbon fiber–carbon fiber powder conductive asphalt concrete with a resistivity of 0.98 Ω·m was finally prepared. In the temperature rise test of the Marshall specimen and rutting slab, its warming effect is obvious, and the heat transformation rate is more than 75%, so it has a very good ability to melt snow and ice.

Evaluation of the effect of different preparation processes on the road performance of thermoplastic resin modified porous asphalt mixtures

In order to evaluate the effects of three preparation processes, namely dry process (DP), wet process (WP) and wet/dry mixing process (MP), and resin high viscosity modifier (RHVM) on the road performance of porous asphalt mixtures, the frequency scanning, multi-stress creep recovery, and bending beam rheometer tests were used to analyze the rheological performance of resin-modified high viscosity asphalt under different processes. Uniaxial compression, Wheel tracking, Semi-circular bending and Freeze-thaw indirect tensile tests were used to test the properties of resin-modified porous asphalt mixtures under different processes. The commonly used TAFPACK-Super (TPS) modifier was a control group. Finally, the changes in the microscopic morphology characteristics and chemical composition were used to illustrate the enhancement mechanism of resin modifiers. The results showed that the high-temperature deformation resistance and low-temperature cracking resistance of RHVM modified asphalt prepared by DP and MP are weaker than that of the WP. Compared to the RHVM(WP), the Jnr(3.2) of RHVM(DP) and RHVM(WP) decreased by 14.3% and 63.8%, the strength modulus of RHVM(DP) and RHVM(MP) increased by 21.5%, 28.0% and the creep rate decreased by 2.37%, 4.45%, respectively. As for the performance of asphalt mixture, compared to the RHVM(WP) asphalt mixture, the dynamic stability of RHVM asphalt mixture prepared by the DP and MP decreased by 17.3–18.2%, σs and εs of RHVM(DP) and RHVM(MP) increased by 15–35% and 21–29%, respectively. The water stability of RHVM(DP) asphalt mixtures was better than that of RHVM(WP) when the mixing time reached 180 s. RHVM(WP) asphalt mixtures have superior low-temperature cracking resistance, comparable water stability, and slightly poorer high-temperature stability than that of TPS(WP) asphalt mixture. Microscopic morphology observation found that some modifier particles and asphalt binder did not realize effective mixing under the DP and MP, and infrared spectroscopy results confirmed that TPS modifiers are mainly physically co-mingled with asphalt, while the tackifier resin in the RHVM reacts with the asphalt to form new functional groups to increase the viscosity of the asphalt.

Systematic assessment of a multi–solid waste cementitious material: Feasibility and environmental impact

This study systematically assessed the feasibility of replacing ordinary Portland cement (OPC) with a multi–solid waste cementitious material (MSC) composed of ground granulated blast furnace slag (GGBS), steel slag (SS), red mud (RM), fly ash (FA), limestone powder (LP), and desulfurized gypsum (DG) in specific proportions of 28%, 25%, 21%, 11.5%, 9%, and 5.5%, respectively. The hydration characteristics were analyzed using hydration heat, XRD, TG–DTG, FTIR, and SEM–EDX tests. The heavy metal content and leaching concentration of the MSC were determined using inductively coupled plasma mass spectrometry (ICP–MS). The unconfined compressive strength (UCS), indirect tensile strength (ITS), and water stability of the MSC-stabilized clayey sand and stone chips were investigated. The results showed that synergistic hydration among multiple solid wastes generated abundant hydration products, including Ca(OH)2, C–(A)–S–H gels, and AFt crystals, which formed dense and compact microstructures. Furthermore, Pb and Cd in the raw material were effectively solidified by MSC hydration, with leaching concentrations as low as 0.181 and 0.002 mg/L, respectively. The contents and leaching concentrations of the other heavy metals were significantly lower than their limits. The pH of the MSC mortar leachate was stable at 11.56 with curing age, which complied with environmental safety standards. Moreover, MSC as a binder demonstrated higher UCS, ITS, and water stability in comparison to OPC. When MSC was added at a 6% dosage to stabilize clayey sand and stone chips, the UCS values measured after 7 days of curing were 2.82 MPa and 4.83 MPa, respectively. Finally, the MSC was successfully applied in practical projects, demonstrating its promising application prospects.

Boosting photoelectrocatalytic oxygen evolution activity of BiVO4 photoanodes via caffeic acid bridged to NiFeOOH

Bismuth vanadate (BiVO4) is a promising n-type photoanode material for photoelectrochemical (PEC) water splitting. However, its activity is impeded by poor charge carrier transport and sluggish oxygen evolution kinetics. In this study, we reports a Fe doping and caffeic acid (CA)/NiFeOOH (NiFe) modification with BiVO4 photoanode (NiFe/CA/Fe-BiVO4) to enhance the PEC water oxidation performance and stability. The modified BiVO4 demonstrates significant advantages in promoting the PEC performance and stability. Specifically, Fe doping via in-situ electro-deposition results in smaller crystal sizes, larger specific surface areas, and more exposed active sites. Furthermore, co-catalyst NiFe connects with Fe-BiVO4 through CA bridge facilitates a more uniform self-assembly distribution of NiFe on BiVO4 surface. The NiFe/CA/Fe-BiVO4 exhibits an excellent photocurrent density of 6.2 mA/cm2 at 1.23 VRHEand demonstrates good stability at 0.8 VRHE. In addition, the composite photoanode shows a high applied bias photon-to-current efficiency (ABPE) value of 2.15% at 0.65 VRHE. EPR and in-situ FTIR confirm the generation of superoxide active species (O2- and ·O2-) during the PEC water oxidation reaction.

Experimental Performance of Filling Material with Modified Red Mud for Roadbed

Cement-modified red mud as roadbed filler was investigated through tests, including compaction, California Bearing Ratio (CBR), modulus of resilience (E0), unconfined compressive strength (UCS), and scanning electron microscopy. Optimum moisture content (ω0), maximum dry density(), CBR, modulus of resilience, UCS, and microscopic characteristics of red mud were analyzed in different modified states. An optimal cement admixture for red mud modification was proposed. Results showed that (1) adding cement significantly improved CBR and modulus of resilience, (2) cement-modified red mud exhibited faster initial strength formation, with 7-day UCS over 65% of 28-day UCS, (3) water stability and frost resistance improved significantly with 4% and 6% cement dosing, (4) recommended cement admixture was 1.1% without adverse conditions, but not less than 6% with water immersion. Modified red mud is unsuitable for seasonal frozen regions. The recommended blending and leaching concentration met regulatory requirements, meeting technical, environmental, and economic goals for roadbed filler in highway construction.

All-natural, hydrophobic, strong paper straws based on biodegradable composite coatings

Plastic-coated paper straws are insufficient to solve the plastic pollution problem because microplastics are formed during their degradation. In this study, upgraded paper straws were prepared by coating with biodegradable sodium alginate/cellulose nanofiber/stearic acid (SA/CNF/STA) on the surface of paper without additional adhesives. The tensile strength of the paper was enhanced synergistically by the coated SA and CNF after cross-linking with Ca2+ ions, reaching a maximum (26.46 MPa) when the mass ratio of SA to CNF was 4:1. The straws were prepared by spirally winding coated paper into tubes. Subsequent STA modification with different concentration (1–40%) improved the water stability of the paper straws. The paper straws exhibited excellent mechanical properties (including 13.45 MPa of flexural strength, 13.30 MPa of compressive strength) and hydrophobicity (103.67° of maximum water contact angle). After 130 days of soil burial, the paper straws were completely degraded. The comprehensive performance of prepared straws exceeds that of commercially available products in the same category, and they are safe and biodegradable. Paper straw in the work is in line with the concept of green and low-carbon development.

Harnessing Pb-S Interactions for Long-Term Water Stability in Cesium Lead Halide Perovskite Nanocrystals.

Lead halide perovskite nanocrystals (LHP NCs) have garnered attention as promising light-harvesting materials for optoelectronics and photovoltaic devices, attributed to their impressive optoelectronic properties. However, their susceptibility to moisture-induced degradation has hindered their practical applications. Despite various encapsulation strategies, challenges persist in maintaining their stability and optoelectronic performance simultaneously. Here, a ligand exchange approach is proposed using (11-mercaptoundecyl)-N,N,N-trimethylammonium bromide (MUTAB) to enhance the stability and dispersibility of CsPbBr3 (CPB) NCs in aqueous environments. MUTAB enables effective surface passivation of the CPB NCs via robust Pb-S interactions at the S-terminal while concurrently directing water molecules through the unbound cationic N-terminal or vice versa, ensuring water dispersibility and stability. Spectroscopic analysis confirms retained structural and optical integrity post-ligand exchange. Crucially, MUTAB-bound CPB NCs exhibit sustained charge transfer properties, demonstrated by aqueous colloidal oxidation reactions. This ligand exchange strategy offers a promising pathway for advancing LHP NCs toward practical optoelectronic and photocatalytic applications.

Replacement of fishmeal by fermented spent coffee ground: Effects on growth performance, feed stability, blood biochemistry, liver, and intestinal morphology of African catfish (Clarias gariepinus)

There has been a consistent interest in the aquaculture industry in the use of plant elements as a substitute for fish meal (FM). The present study aimed to examine the impact of substituting FM with varying proportions of fermented spent coffee grounds (FCG) on the growth performance, feed stability, blood biochemistry, liver, and intestinal histology of African catfish, Clarias gariepinus. Five isonitrogenous diets were formulated with a crude protein content of 32 %. These diets were created with different percentages of FM replacement, specifically 0 % (T1), 10 % (T2), 20 % (T3), 40 % (T4), and 80 % (T5). The fish were then fed these diets for a duration of 70 days. The results showed that fish provided with 10 % FCG (T2) gave the highest improvement (p < 0.05) in growth conditions compared with other treatments. The feed’s physical properties were varying, but floatability and water stability were highest in T2 diets. Total bacteria (TB) in feed and intestine were more elevated in fish fed with 10 % FCG compared to other treatments. The histopathological damage in the intestine and liver morphology was observed when the level of inclusion of FCG was increased in all treatments. In addition, T2 gave the highest value (p < 0.05) in villus length, width, and crypt depth. Some parameters were improved in both blood haematology and blood biochemical parameters, and T2 gave the highest value (p < 0.05) in white blood cells, lymphocytosis, monocytes, red blood cells, haemoglobin, albumin, globulin, total protein, and creatine. In summary, the substitution of 10 % FCG with FM holds potential for application within the aquafeed sector, as it has been observed to contribute to enhanced growth and improved health conditions in African catfish and other freshwater species.

Multilevel Information Encryption Based on Thermochromic Perovskite Microcapsules via Orthogonal Photic and Thermal Stimuli Responses.

Increasing modal variations of stimulus-responsive materials ensure the high capacity and confidentiality of information storage and encryption systems that are crucial to information security. Herein, thermochromic perovskite microcapsules (TPMs) with dual-variable and quadruple-modal reversible properties are designed and prepared on the original oil-in-fluorine (O/F) emulsion system. The TPMs respond to the orthogonal variations of external UV and thermal stimuli in four reversible switchable modes and exhibit excellent thermal, air, and water stability due to the protection of perovskites by the core-shell structure. Benefiting from the high-density information storage TPMs, multiple information encryptions and decryptions are demonstrated. Moreover, a set of devices are assembled for a multilevel information encryption system. By taking advantage of TPMs as a "private key" for decryption, the signal can be identified as the corresponding binary ASCII code and converted to the real message. The results demonstrate a breakthrough in high-density information storage materials as well as a multilevel information encryption system based on switchable quadruple-modal TPMs.

Boron nanoparticles (BNPs) produced by ns-laser ablation in water: synthesis and characterization

Boron nanoparticles (BNPs) are attractive nanomaterials for their employment in many applications, such as neutron detection, boron neutron capture therapy, proton boron capture therapy and nuclear fusion. Depending on the specific application, 10B or 11B isotopes can be used.Nevertheless, there are significant challenges in developing suitable BNPs using both conventional chemical synthesis routes and dry fabrication techniques. In this study we report BNPs directly synthetised in water by pulsed Laser Ablation in Liquid (PLAL). Nanoparticles of elemental boron have been generated by laser ablation of a sintered 10B target in MilliQ water by employing ns laser pulse. The ablation resulted in BNPs and boron target micro-fragments with hydrogen gas and boric acid as by-products. Simple washing steps were used to obtain clean BNPs in water. The BNPs showed a narrow size distribution between 3 and 4 nm and their stability in water was induced by a thin layer of boron oxide surrounds BNPs. The BNPs were fully characterized by the chemical and structural point of view employing several techniques. A discussion on boron chemical reactions during laser ablation in water and after the NPs were released in solution was done.

Postsynthetically Modified Alkoxide‐Exchanged Ni2(OR)2BTDD: Synergistic Interactions of CO2 with Open Metal Sites and Functional Groups

AbstractPostsynthetic modifications (PSMs) of metal–organic frameworks (MOFs) play a crucial role in enhancing material performance through open metal site (OMS) functionalization or ligand exchange. However, a significant challenge persists in preserving open metal sites during ligand exchange, as these sites are inherently bound by incoming ligands. In this study, for the first time, we introduced alkoxides by exchanging bridging chloride in Ni2Cl2BTDD (BTDD=bis (1H‐1,2,3,–triazolo [4,5‐b],–[4′,5′‐i]) dibenzo[1,4]dioxin) through PSM. Rietveld refinement of synchrotron X‐ray diffraction data indicated that the alkoxide oxygen atom bridges Ni(II) centers while the OMSs of the MOF are preserved. Due to the synergy of the existing OMS and introduced functional group, the alkoxide‐exchanged MOFs showed CO2 uptakes superior to the pristine MOF. Remarkably, the tert‐butoxide‐substituted Ni_T exhibited a nearly threefold and twofold increase in CO2 uptake compared to Ni2Cl2BTDD at 0.15 and 1 bar, respectively, as well as high water stability relative to the other exchanged frameworks. Furthermore, the Grand Canonical Monte Carlo simulations for Ni_T suggested that CO2 interacts with the OMS and the surrounding methyl groups of tert‐butoxide groups, which is responsible for the enhanced CO2 capacity. This work provides a facile and unique synthetic strategy for realizing a desirable OMS‐incorporating MOF platform through bridging ligand exchange.

Tuning Surface, Phase, and Magnetization of Superparamagnetic Magnetite by Ionic Liquids: Single-Step Microwave-Assisted Synthesis.

Achieving colloidal and chemical stability in ferrofluids by surface modification requires multiple steps, including purification, ex situ modification steps, and operation at high temperatures. In this study, a single-step microwave-assisted methodology is developed for iron oxide nanoparticle (IONP) synthesis utilizing a series of imidazolium-based ionic liquids (ILs) with chloride, bis(trifluoromethylsulfonyl)imide, and pyrrolide anions as the reaction media, thus eliminating the use of volatile organics while enabling rapid synthesis at 80 °C as well as in situ surface functionalization. The characterized surface functionality, hydrodynamic particle size, magnetization, and colloidal stability of the IONPs demonstrate a strong dependence on the IL structure, ion coordination strength, reactivity, and hydrophilicity. The IONPs present primarily a magnetite (Fe3O4) phase with superparamagnetism with the highest saturation magnetization at 81 and 73 emu/g at 10 and 300 K, respectively. Depending on the IL coating, magnetization and exchange anisotropy decrease by 20 and 2-3 emu/g (at 35 wt % IL), respectively, but still represent the highest magnetization achieved for coated IONPs by a coprecipitation method. Further, the surface-functionalized superparamagnetic magnetite nanoparticles show good dispersibility and colloidal stability in water and dimethyl sulfoxide at 0.1 mg/mL concentration over the examined 3 month period. This study reports on the intermolecular and chemical interactions between the particle surface and the ILs under synthetic conditions as they relate to the magnetic and thermal properties of the resulting IONPs that are well suited for a variety of applications, including separation and catalysis.

Tailoring Charge Flow in Carbon-Defective Cu-MOF with Pd Nanoparticles: A Boost for Visible Light Organic Photoelectrochemical Transistor in Bioanalysis.

The photoactive material was of significant importance in organic photoelectrochemical transistor (OPECT) bioanalysis as it influences the photoinduced voltage and the μC* product, resulting in a varying sensor sensitivity. The utilization of metal-organic frameworks (MOFs) as photoactive materials in OPECT analysis is promising, yet it remains a grand challenge due to the inherently narrow light absorption range and high electron-hole recombination rate. Herein, Pd NPs were encapsulated as electron acceptors into the Cu-MOF using a double-solvent method, followed by pyrolysis at the proper temperature. After pyrolysis, Cu-MOF transformed into a carbon defect-rich composite of CuO and Cu2O while retaining its high porosity and structural morphology. The resulting carbon defect-rich pyrolysis Cu-MOF (p-Cu-MOF) served as an active support, facilitating the separation of electrons and holes. The photoelectrons trigger the electron transfer of adjacent active metal components and the formation of a Schottky junction between Pd and the MOFs. This effect induces the electron donation from the MOFs. Moreover, Pd/pyrolysis Cu-MOF exhibits significantly higher visible light absorption, better water stability, and higher electrical conductivity compared to Cu-MOF and Pd/Cu-MOF. An OPECT sensor was fabricated by utilizing Pd/p-Cu-MOF as the photoactive material and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as the channel material on an integrated laser-etched FTO. The aptamer was used as the recognition element, enabling sensitive and efficient detection of residual isocarbophos.

Highly Specific Sulfadiazine Detection Using a Two-Dimensional Europium-Organic Coordination Polymer.

Sulfadiazine (SFZ) is an inexpensive large-consumption antibiotic used for treat bacterial infections but an excess of residues in food can be harmful. Fast and specific luminescence detection of SFZ is highly challenging because of the interference of structurally similar antibiotics. In this work, we develop a two-dimensional europium-organic coordination polymer with excellent luminescence and water stability for highly specific detection of SFZ in the range of 0-0.2 mM. Structural analysis shows that the high stability of coordination polymer is due to the high coordination number of europium ion and the special chelating coordination structure of ligand. The experiment results revealed that the high selectivity and effectively luminescence quenched behaviour of coordination polymer toward SFZ is caused by highly efficient inner filter effect.

Micro-macro performance evolution behavior of fine-grained porous asphalt mixture exposed to ultraviolet-water-heat-load coupling action

In the Yangtze River Delta of China, porous asphalt pavement is significantly affected by UV radiation, water, heat, and traffic load. Therefore, research on its long-term performance evolution behavior under multi-factor coupling effect contributes to conducting engineering practice. The key pavement performance evolution of fine-grained porous asphalt mixture (PA-13), using SBS/crumb rubber (CR) composite modifier or TPS modifier, with multiple void ratios was studied. The evolution of high-temperature stability, water stability, and meso-drainage performance of PA-13, among the simulated 5-year service process, was respectively evaluated by dynamic creep test, immersion Marshall test, CT scanning and three-dimensional reconstruction. The findings demonstrate that the negative impacts of coupled conditions are mainly concentrated in the later stage of service. Under cyclic effect, the good anti-permanent deformation ability of SBS/CR PA-13 helps to alleviate the attenuation of its void structure and permeability. Besides, the transverse connectivity of void is more obvious than the vertical connectivity throughout the entire service process. In general, SBS / CR PA-13 has better anti-attenuation ability than TPS PA-13 in high temperature stability, water stability and drainage performance, indicating SBS/CR porous asphalt mixture is more suitable for application in high temperature and rainy areas.