Poly Diallyldimethylammonium Chloride Research Articles

Multifunctional composite phase change material with electrostatic self-assembly structure based on carboxylated multi-walled carbon nanotubes

The need for improved thermal regulation in electronic devices and solar thermal energy storage, prompted by the energy crisis, has expedited the advancement of phase change materials (PCMs). Carboxylated multi-walled carbon nanotubes (MWCNT-COOH) were produced by introducing carboxyl functional groups onto MWCNTs utilizing a concentrated acid treatment. The novel composite was engineered through an electrostatic self-assembly process between the negatively charged MWCNT-COOH and the positively charged Poly dimethyl diallyl ammonium chloride (PDDA) solution, filling the structure with the PCM polyethylene glycol (PEG) and incorporating the (magnesium hydrate) Mg(OH)2 to enhance the material's flame resistance at high temperatures. The thermal conductivity of the obtained composites improved significantly from 0.25 W/m·K to 1.183 W/m·K, while maintaining an enthalpy of phase transition of phase change of 135.1 J/g. Owing to the capillary effect of the closely packed MWCNT-COOH tubular structure, the composite material exhibited excellent high-temperature shape retention ability. Additionally, the composite demonstrated high absorption with an absorbance reaching 1.18 L/(g·cm) and composite materials can convert up to 86.8 % of light energy into heat energy.

A cationic polyelectrolyte for enhancing dewatering of montmorillonite-containing coal slime: adsorption and modification mechanism

ABSTRACT In this study, a cationic polyelectrolyte (Poly dimethyl diallyl ammonium chloride, PDADMAC) was introduced as a filter aid to enhance the dewatering effect of montmorillonite (MT)-containing coal slime, and compared with cationic polyacrylamide (CPAM). The dewatering performance of PDADMAC and CPAM was evaluated based on vacuum filtration experiments. The modification mechanism of PDADMAC on Mt particle surface was revealed by filter cake pore distribution, zeta potential, contact angle and Atomic Force Microscopy (AFM). The adsorption difference between PDADMAC and CPAM on Mt surface was studied by Density Functional Theory (DFT). In addition, DLVO theory further explains the mechanism of PDADMAC enhancing dewatering from the perspective of interaction force. The optimal dosage of PDADMAC was 125 g/t, and the filter cake moisture content was reduced by 3%. Compared to CPAM, PDADMAC achieves efficient dewatering at a lower dosage. PDADMAC has a more prominent ability to neutralize charge, and its effect on interparticle interactions was a potential mechanism to promote dehydration.

Synergistic enhancement of dewatering of montmorillonite-containing coal slime by novel combined filter aid: an experimental and simulation study

ABSTRACT The efficient dewatering of montmorillonite (Mt)-containing coal slime is still an urgent problem to be solved in coal preparation plant. In this study, the dewatering effect of poly(o-phenylenediamine)/Poly dimethyl diallyl ammonium chloride (POPD/PDADMAC) combined filter aid on Mt-containing coal slime was studied. The dewatering performance of combined filter aid was investigated by vacuum filtration test. The action mechanism of combined filter aid was revealed by contact angle, zeta potential, cake pore and atomic force microscope (AFM). The co-adsorption principle of the combined filter aid was elucidated based on density functional theory (DFT) and molecular dynamics simulation (MD). Compared to PDADMAC, the combined filter aid has better performance for dewatering of Mt-containing coal slime, and has the advantage of low reagent dosage. The combined filter aid can greatly reduce the Mt potential, increase the Mt contact angle, and increase the porosity of the filter cake. There was a co-adsorption effect between the combined filter aid. Specifically, there were ion–dipole interaction, cation–π interaction and Cl ions bridged electrostatic interaction between POPD and PDADMAC. This study has developed a novel combined filter aid, which provides theoretical and technical support for the high-efficiency pressure filtration dewatering of Mt-containing coal slime in coal preparation plants.

Self-assembled conductive coating and bifacial microstructures Collaboratively Adjusting the sensing performance and high reliability of the flexible pressure sensors

Flexible pressure sensors are being studied intensively for applications such as smart wearables and health monitoring. While ensuring the excellent sensing performance, the reliability (durability and environmental resistance) of the sensors are also key indicators that determine whether they can be used in practice. In this research, a strategy to adjust the sensing performance and high reliability of the flexible pressure sensors by self-assembled conductive coating and bifacial microstructures (BM) is proposed. Polydimethylsiloxane/carbon nanotube films with BM are first modified to reduce the surface contact angle. Then poly(dimethyl diallyl ammonium chloride) (PDAC) and hydroxylated carbon nanotubes/carboxylated cellulose nanofibers/glycerol (CNT-OH/CNF-C/GL) are successively assembled on the BM surface to construct conductive coatings (PCCG). The sensor based on PCCG and BM (the PCCG-BM sensor) shows a high sensitivity (9.97 kPa−1), a wide detection range (0–330 kPa), and a fast response time (59 ms). The PCCG-BM sensor has excellent repeatability, and it still outputs stable current change signals after 240,000 pressure cycles. What’s more, the PCCG-BM sensor is treated with extreme environments such as bending, stretching, washing, and high pressure, and the sensor still maintains excellent performances. This preparation strategy provides a new perspective for the fabrication of high-performance and high-reliability flexible sensors.

Efficient removal of per- and polyfluoroalkyl substances (PFASs) from stored rainwater by composite metal salt /polydimethyldiallylammonium chloride coagulants

Stored rainwater, the primary source of drinking water in the villages and towns of the Loess Plateau in northwest China, has been found to contain per- and polyfluoroalkyl substances (PFASs) and lacks necessary treatment measures. Coagulation is a common water treatment process, and enhancing its efficacy in removing PFASs can significantly improve treatment efficiency, reduce costs, and minimize the environmental and health risks associated with perfluorinated compounds. This study investigated the removal efficiency of perfluorobutanoic acid (PFBA), perfluorobutanesulfonic acid (PFBS), perfluorooctanoic acid (PFOA), and perfluorooctanesulfonic acid (PFOS) using inorganic salt coagulants alone and in combination with polydimethyldiallylammonium chloride (PDMDAAC). The results indicated that the removal efficiencies of the four PFASs by polyferric chloride (PFCl) and polyaluminum chloride (PACl) increased with alkalinity. PDMDAAC significantly enhanced the coagulation removal efficiency of the four PFASs. The removal efficiency of the four PFASs was highest when the raw water pH was near 7. Within the molecular weight range of 0–500,000 for PDMDAAC, the removal efficiency of the four PFASs increased with increasing molecular weight. Charge neutralization is the primary coagulation mechanism for the removal of anionic PFASs. Therefore, this study provides guidance for selecting coagulants to remove PFASs from stored rainwater.

The molecular picture of the local environment in a stable model coacervate.

Complex coacervates play essential roles in various biological processes and applications. Although substantial progress has been made in understanding the molecular interactions driving complex coacervation, the mechanisms stabilizing coacervates against coalescence remain experimentally challenging and not fully elucidated. We recently showed that polydiallyldimethylammonium chloride (PDDA) and adenosine triphosphate (ATP) coacervates stabilize upon their transferto deionized (DI) water. Here, we perform molecular dynamics simulations of PDDA-ATP coacervates in supernatant and DI water, to understand the ion dynamics and structure within stable coacervates. We found that transferring the coacervates to DI water results in an immediate ejection of a significant fraction of small ions (Na+ and Cl-) from the surface of the coacervates to DI water. We also observed a notable reduction in the mobility of thesecounterions incoacervates whenin DI water, both in the cluster-forming and slab simulations, together with a lowered displacement of PDDA and ATP. These results suggest that the initial ejection of the ions from the coacervates in DI water may induce an interfacial skin layer formation, inhibiting further mobility of ionsin the skin layer.

Selective mycobacterial capture with ultraviolet-polymerized poly-dimethyldiallyl chloride functionalized surfaces

Tuberculosis (TB) is the top cause of death from a single infectious pathogen after COVID-19. Despite molecular diagnostic advances, two-thirds of the 10 million annual TB cases are still diagnosed using direct smear microscopy which has ~50% sensitivity. To increase the analytical performance of smear microscopy, we developed and characterized a novel polymer (Polydiallyldimethylammonium chloride [PDADMAC]) engraftment on inexpensive polystyrene (PS) specifically functionalized for mycobacterial capture. Engraftment is achieved via UV photopolymerization of DADMAC monomer on plasma-activated PS. The platform was tested on sputum from presumptive TB cases in Kampala, Uganda (n = 50), with an increased overall sensitivity of 81.8% (27/33) vs. fluorescent smear microscopy 57% (19/33) compared to a molecular (Cepheid GeneXpert MTB/RIF) gold standard. Frugal smear diagnostic innovation that is rapid and does not require dedicated instrumentation may offer an important solution to bridge the TB diagnostic gap.Graphical

Interaction of poly dimethyl diallyl ammonium chloride with sludge components: Anaerobic digestion performance and adaptive changes of anaerobic microbes

The wide utilization of poly dimethyl diallyl ammonium chloride (polyDADMAC) in industrial conditions leads to its accumulation in waste activated sludge (WAS), thereby affecting subsequent WAS treatment processes. This work investigated the interaction between polyDADMAC and WAS components from the perspective of anaerobic digestion (AD) performance and anaerobes adaptability variation. The results showed that polyDADMAC decreased the content of biodegradable organic substrates (i.e., soluble protein and carbohydrate) by binding with the functional groups and then settling to the solid phase, thus impeding the subsequent utilization. Higher concentrations of polyDADMAC prompted an initial protective response of excreting organic substrates into extracellular environment, but its toxicity to archaea was irreversible. Consequently, polyDADMAC inhibited the processes of AD and induced a 30 % reduction in methane production with 0.05 g polyDADMAC/g total suspended solid (TSS) addition. Changes in microbial community structure indicated that archaea involved in methane production (e.g., Anaerolineaceae sp. and Methanosaeta sp.) were inhibited when exposed to polyDADMAC. However, several adaptive bacteria with the ability of utilizing complex organics and participating in nitrogen cycle (e.g., Aminicenantales sp. and Ellin6067 sp.) were enriched with the above dosage. Specifically, the decreased abundance of genes relevant to methane metabolism pathway (i.e., mer and cdh) and increased abundance of genes involved in metabolism of cofactors and vitamins (e.g., nad and thi) indicated the toxicity of polyDADMAC and the irritant response of microflora. Moreover, polyDADMAC underwent degradation in AD system, resulting in a 12 % reduction in 15 days, accompanied by an increase in the -NO2 functional group. In general, this study provided a thorough understanding of the interaction between polyDADMAC and WAS components, raising concerns regarding the elimination of endogenous pollutants during AD.

Identifying Root Origin of Insulating Polymer Mediated Solar Water Oxidation.

Rational construction of high-efficiency photoelectrodes with optimized carrier migration to the ideal active sites, is crucial for enhancing solar water oxidation. However, complexity in precisely modulating interface configuration and directional charge transfer pathways retards the design of robust and stable artificial photosystems. Herein, a straightforward yet effective strategy is developed for compact encapsulation of metal oxides (MOs) with an ultrathin non-conjugated polymer layer to modulate interfacial charge migration and separation. By periodically coating highly ordered TiO2 nanoarrays with oppositely charged polyelectrolyte of poly(dimethyl diallyl ammonium chloride) (PDDA), MOs/polymer composite photoanodes are readily fabricated under ambient conditions. It is verified that electrons photogenerated from the MOs substrate can be efficiently extracted by the ultrathin solid insulating PDDA layer, significantly boosting the carrier transport kinetics and enhancing charge separation of MOs, and thus triggering a remarkable enhancement in the solar water oxidation performance. The origins of the unexpected electron-withdrawing capability of such non-conjugated insulating polymer are unambiguously uncovered, and the scenario occurring at the interface of hybrid photoelectrodes is elucidated. The work would reinforce the fundamental understanding on the origins of generic charge transport capability of insulating polymer and benefit potential wide-spread utilization of insulating polymers as co-catalysts for solar energy conversion.

A green UV-resistant Natural rubber-Polydopamine-TiO2@SiO2 composite with high mechanical properties based on an electrostatic adsorption effect

Abstract Antioxidants are usually added into the natural rubber (NR) to resist the oxidation caused by the ultraviolet (UV) irradiation, while commonly used antioxidans are usually organic and prone to decomposition and migration. The inorganic UV absorbers like titanium dioxide nanoparticles (TiO2) and silicon dioxide (SiO2) can maintain chemical stability under UV radiation, while the hydroxyl radicals from electron-hole pairs in TiO2 would damage NR matrix and the poor compatibility of TiO2 with NR limited the process. Therefore, inert SiO2 is coated on TiO2 (TiO2@SiO2) to reduce its photocatalytic activity, and polydopamine (PDA) is coated on rubber to improve stability. The strong light-absorbing properties of PDA could also improve the UV-resistant ability of NR. Besides, poly (sodium-p-styrenesulfonate) (PSS) coating NR-PDA provides the matrix negative charge, and polydiallyl dimethyl ammonium chloride (PDDA) wrapped around TiO2@SiO2 can give a positive charge, thus moderating the compatibility between the filler and the matrix through electrostatic adsorption. The green UV-resistant natural composite NR-PDA TiO2@SiO2 was fabricated. The composites exhibited strong tensile strength and excellent UV-resistant properties, which particularly extend the service life of rubber products as UV-shielding materials, thus showing significant potential in extreme environments.

Nest-shaped hollow-encapsulated Pd catalyst enhances the catalytic performance of hydrogen peroxide directly synthesizing from hydrogen and oxygen

A well-defined structural morphology can significantly construct a special catalytic micro-reaction environment to enhance the catalytic performance of Pd catalyst in the direct synthesis of hydrogen peroxide from hydrogen and oxygen (DSHP). In this study, SiO2 was used as a rigid template, PdCl2 as the Pd precursor, and dopamine hydrochloride (DA) as the carbon and nitrogen source to synthesize a nest-shaped hollow-encapsulated Pd catalyst named PdMulti@ONHCS. This catalyst was successfully constructed via high-temperature pyrolysis of poly dimethyl diallyl ammonium chloride (PDDA), which generated a blasting effect crucial for this formation. Characterization analysis, catalytic performance evaluation experiment, and molecular dynamics simulation were conducted to explore the structure-performance relationship of PdMulti@ONHCS catalyst in DSHP. Both experimental and simulation results consistently showed that the nest-shaped hollow structure of PdMulti@ONHCS catalyst created a distinctive catalytic microreactor environment with a spatial mass transfer constraint, which was not only conducive to adsorption and enrichment of H2 and O2 at Pd active sites to produce H2O2. In addition, the generated H2O2 can be desorbed from Pd active sites in time and rapidly diffused into the reaction solution, effectively inhibiting the dissociation of species containing OO bonds on the Pd surface, resulting in severe hydrogenation and decomposition side reactions, and improving H2O2 productivity and selectivity.

Optimization of electrostatic seeding technique for wafer-scale diamond fabrication on β-Ga2O3

Integrating diamonds with β-Ga2O3 is a promising solution for addressing the problem of poor thermal conductivity and limited p-type dopability of β-Ga2O3. However, growing diamonds on β-Ga2O3 is challenging, especially without any interfacial layer, and achieving large-scale uniform diamond films is also tricky. This paper explores the vital role of an electrostatic seeding technique involving the use of Polydiallyldimethylammonium chloride (PDDAC) polymer with a positive zeta potential and diamond nano slurries with a negative zeta potential to facilitate the integration of diamond with β-Ga2O3. We conduct a detailed analysis of each step of this seeding technique, adjusting the spinning speed of the polymer coating, spinning period, baking period, and ultrasonication period to understand the underlying mechanisms preventing large-scale diamond growth and to identify strategies for achieving wafer-scale diamond fabrication on single crystal β-Ga2O3 film. This process facilitates the attainment of a uniform dispersion of diamond nanoparticles on β-Ga2O3 at a seeding density of ∼1.82 × 1011 cm−2. The optimized seeding technique has enabled the successful growth of wafer-scale diamond films on β-Ga2O3, as confirmed by scanning electron microscopy (SEM). Additionally, the high quality of the diamond film is affirmed by a quality factor of 96.75 % and a narrow full-width half maximum of 10.28 cm−1 in the T2g peak of the Raman spectra. The X-ray diffraction pattern reinforces the excellent quality of polycrystalline diamond films with minimum stress. In summary, this research provides valuable insights into the polymer-assisted electrostatic seeding technique, paving the way for the uniform growth of wafer-scale diamond films on β-Ga2O3, which is critical for realizing β-Ga2O3-based heterostructure devices.

SERS as a tool for determination of structurally related compounds: The case of sulfanilamide class antibiotics

Analysis of real objects based on surface-enhanced Raman spectroscopy (SERS) often utilizes new SERS substrates and/or complex analysis procedures, and they are optimized for only the determination of a single analyte. Moreover, analysis simplicity and selectivity are often sacrificed for maximum (sometimes unnecessary) sensitivity. Consequently, this trend limits the versatility of SERS analysis and complicates its practical implementation. Thus, we have developed a universal, but simple SERS assay suitable for the determination of structurally related antibiotics (five representatives of the sulfanilamide class) in complex objects (human urine and saliva). The assay involves only mixing of acidified analyzed solution with co-activating agent (polydiallyldimethylammonium chloride – PDDA) and SERS substrate (standard colloidal silver nanoparticles). Acidification promotes the generation of SERS spectra with maximum similarity and intensity, which is explained by the favorable enhancement of the protonated sulfanilamide moiety (a structurally similar part of the studied antibiotics) as a result of its strong electrostatic interaction with the SERS-active surface. Meanwhile, the addition of PDDA improves analysis selectivity by reducing background signal from body fluids, enabling to simplify sample pretreatment (dilution for urine; mucin removal and dilution for saliva). Therefore, the assay allows for rapid (≤10 min), precise, and accurate class-specific determination of sulfanilamides within concentration ranges suitable for non-invasive therapeutic drug monitoring in urine (40–600 μM) and saliva (10–30 μM). We also believe that thorough investigation of structurally related analytes and accompanying effects (e.g., high spectral similarity) is a promising direction to improve the understanding of SERS in general and expand its capabilities as an analytical tool.

Comparative analysis of parent and modified ZSM-5 zeolites: Insights from positron annihilation lifetime spectroscopy

Modified zeolite ZSM-5 samples were prepared by synthesis in the presence of the organics acting as mesoporogens: cationic surfactant, hexadecyltrimethylammonium bromide (CTAB) and cationic polymer, polydiallyldimethylammonium chloride (PDADMAC), as well as by alkali etching of the parent zeolite. Properties of modified zeolites were compared to the parent ZSM-5 zeolite. X-ray diffractograms demonstrate that the obtained modified zeolite ZSM-5 samples in all cases have preserved parent crystalline zeolite framework of the MFI-type. However, scanning electron micrographs of the same samples show morphology variations of the modified samples as compared to the starting zeolite. Thermogravimetric analyses show distinct weight loss curves of the samples. Differences have been also noted in the hydroxyl stretching range of the infrared spectra, and in the results of positron annihilation lifetime spectroscopy (PALS) measurements, which indicated dissimilarities by probing free volume in parent and modified zeolite ZSM-5 samples. In that way, PALS as scarcely used technique in zeolite studies, proved its applicability in structural investigation of this kind.

Enhancing the efficiency of hemp fiber dyeing with natural dyes: Indigo and lac

Hemp fibers dyed with natural dyes are environmentally sustainable, but it is typically difficult to achieve an intense shade and washing durability. In this study, mercerization and cationization using polyelectrolyte, Poly-diallyldimethylammonium chloride (polyDADMAC), were chosen to enhance the dyeing efficiency and mechanical properties. Indigo and lac were chosen as natural dyes due to their widespread use. SEM demonstrated that untreated fibers contained the non-cellulose boundary layer on the surfaces, but after mercerization, the surfaces were smoother, making them suitable for absorbing natural dyes. In agreement with the FT-IR, the spectra of non-cellulose disappeared after mercerizing. Following cationization, the FT-IR spectra confirmed the consequences of using poly-DADMAC. Tensile testing demonstrated that mercerized hemp yarns were 34.1% stronger compared to untreated hemp yarns due to the decrease in non-cellulose content and that the intermolecular attraction of cellulose was not disturbed. The color strength and fastness properties were described by the K/S value. Mercerization considerably affected the K/S of indigo dyeing, while cationization affected lac dyeing significantly. Besides that, both treatments improved fastness properties as well.

Crosslinked Polydiallyldimethylammonium Chloride Adsorbent for the Selective Separation of Rhenium Ions from Pregnant Leach Solutions.

The depletion of valuable mineral reserves has rendered effluents generated from mining and industrial processing activities a promising resource for the production of precious elements. The synthesis and improvement of new adsorbents to extract valuable compounds from industrial wastes and pregnant leach solutions, besides increasing wealth, can play a significant role in reducing environmental concerns. In this work, a new and low-cost adsorbent for the selective extraction of rhenium (perrhenate ions, ReO4-) was synthesized by the free-radical polymerization (FRP) of a diallyl dimethylammonium chloride monomer (quaternary amine) in the presence of a crosslinker. Various methods were employed to characterize the polymeric adsorbent. The results revealed that the designed polymeric adsorbent had a high surface area and pores with nano-metric dimensions and a pore volume of 6.4 × 10-3 cm3/g. Four environments-single, binary, multicomponent, and real solutions-were applied to evaluate the adsorbent's performance in the selective separation of Re. Additionally, these environments were used to understand the behavior of molybdenum ions, the primary competitors of perrhenate ions in the ion exchange process. In competitive conditions, using variations in qe,mix/qe, an antagonism phenomenon (qe,mix/qe < 1) occurred due to the inhibitory effect of surface-adsorbed molybdenum ions on the binding of the perrhenate ions. However, across all conditions, the separation values for Re were higher than those for the other studied elements (Mo, Cu, Fe).

Synthesis of hierarchical ZSM‐5 using polymer macro template for selective C‐alkylation of m‐cresol with tert‐butanol

AbstractThe present study reports nanocrystalline hierarchical zeoite ZSM‐5 as a potential alternative to homogeneous catalysts for the liquid phase tert‐butylation of m‐cresol. Polydiallyldimethylammonium chloride macro‐template was used to develop vacuum‐concentration dual template nano‐precursors by hydrothermal process. The catalytic performance was analyzed for the given reaction and the high percent conversion of reactants with excellent selectivity towards the ortho isomer, 2‐tert‐butyl‐5‐methylphenol was recorded. In contrast, the low activity and selectivity towards the tert‐butylation of m‐cresol, and the selectivity towards the desired product are noticed with the nanocrystalline zeolite ZSM‐5 synthesized without macro‐template. In addition, the catalyst is recoverable due to its robust nature, which indirectly reduces industrial wastage. Various parameters that affect the rate of the reaction were optimized. Kinetic analysis studies showed that the reaction followed first‐order kinetics with respect to tert‐ and the reaction obeyed the Langmuir‐Hinselwood mechanism. The activation energy was determined as 43.0 ± 0.2 kJ/mole. The study reveals that nanocrystalline hierarchical zeolite ZSM‐5 is an efficient, selective, simple, economical and environment‐friendly catalyst for the tert‐butylation of m‐cresol.

Controllable Synthesis of Titanium Silicon Molecular Zeolite Nanosheet with Short b-Axis Thickness and Application in Oxidative Desulfurization.

Titanium silicon molecular zeolite (TS-1) plays an important role in catalytic reactions due to its unique nanostructure. The straight channel on TS-1 was parallel to the orientation of the short b-axis and directly exposed to the aperture of the 10-member ring with a diameter of 0.54 nm × 0.56 nm. This structure could effectively reduce the diffuse restriction of bulk organic compounds during the oxidative desulfurization process. As a kind of cationic polymer electrolyte, polydimethyldiallyl ammonium chloride (PDDA) contains continuous [C8H16N+Cl-] chain segments, in which the Cl- could function as an effective structure-directing agent in the synthesis of nanomaterials. The chain of PDDA could adequately interact with the [0 1 0] plane in the preparation process of zeolite, and then the TS-1 nanosheet with short b-axis thickness (6 nm) could be obtained. The pore structure of the TS-1 nanosheet is controlled by regulating the content of PDDA. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), N2 physical adsorption analysis, infrared absorption spectrum and ultraviolet-visible spectrum were used to determine the TS-1. The thinner nanosheets exhibit excellent catalytic performance in oxidative desulfurization of dibenzothiophene (DBT), in which the removal rate could remain at 100% after three recycles. Here, the TS-1 nanosheet with short b-axis thickness has a promising future in catalytic reactions.

Polyurethane-Encapsulated Biomass Films Based on MXene@Loofah Sponge for Piezoresistive Pressure Sensor Applications.

Multifunctional wearable electronic sensors exhibit significant potential for applications in health management, motion tracking, intelligent healthcare, etc. In this study, we developed a novel assembly method for a polymeric silver nanowire (Ag NW)/transition metal carbide/nitride (MXene) @Loofah device using a facile solution dip-coating technique. During the pretreatment phase, the loofah was conditioned with polydiallyldimethylammonium chloride (PDAC), promoting the self-assembly of MXene layers and bolstering device stability. Then, the Ag NWs/MXene@Loofah was packaged with polyurethane to form a piezoresistive pressure sensor, which demonstrated superior pressure-sensing capabilities and was adept at registering movements of human joints and even subtle pulses. The design strategy presents a novel and rational approach to developing efficient pressure sensors.

Self-healing and corrosion-sensing multifunctional coatings containing pH-sensitive TiO2-based composites

Polyelectrolyte-encapsulated nanocontainers can effectively respond to changes of pH and thus control the on-demand release of corrosion inhibitors. A pH-responsive release system (Phen-Tpp@MTNs-PDDA) was developed based on the cationic polyelectrolyte poly dimethyl diallyl ammonium chloride (PDDA) encapsulated mesoporous TiO2 nanocontainers (MTNs) loaded with 1,10-phenanthroline (Phen) and tripolyphosphate ions (Tpp) corrosion inhibitors. The epoxy coating (EP) embedded with Phen-Tpp@MTNs-PDDA (Phen-Tpp@MTNs-PDDA/EP) demonstrates superior self-healing properties and confers long-term protection on the metal substrate through the cooperative effect of Phen and Tpp. Simultaneously, this hybrid coating is endowed with corrosion sensing capability based on the color development originating from the interaction of Phen and carbon steel. This self-healing and corrosion-sensing multifunctional coating provides an effective strategy for the corrosion protection of metals.