Slow Rate Research Articles

Approaching Ultimate Synthesis Reaction Rate of Ni-Rich Layered Cathodes for Lithium-Ion Batteries

HighlightsA series of layered oxide cathode materials were synthesized by high-temperature shock strategy for the first time.The approaching ultimate solid reaction rate of the layered nickel-rich layered oxide LiNixCoyMnzO2 was investigated for the first time. Ultrafast average reaction rate of phase transition from Ni0.6Co0.2Mn0.2(OH)2 to Li-containing oxides is 66.7 (% s-1), that is, taking only 1.5 s.

Drastically Accelerated Radical Recombination Kinetics of a Hexaarylbiimidazole Derivative.

More than 60 years have passed since the discovery of hexaarylbiimidazole (HABI), which exhibits a characteristic photochromism that produces colored lophyl radicals through a radical dissociation reaction induced by light irradiation and reverts to its original state through a radical recombination reaction in the dark. Lophyl radicals are relatively stable among organic radicals, have low reactivity with oxygen, and have a very slow radical recombination reaction rate. HABI has been used industrially as a photoinitiator to date. However, the guidelines for molecular design to accelerate the thermal reverse reaction of HABI are still unknown and remain a challenge. We found that suppressing the rotation of the phenyl groups attached to the 4- and 5-positions of the imidazole ring of HABI is effective in accelerating the radical recombination reaction. The simple molecular design strategy to accelerate the thermal reverse reaction of HABI is expected to improve the performance of photoinitiators and photoresponsive materials that utilize HABI as a photoresponsive unit.

The relationship of rate and pause features to the communicative participation of people living with ALS.

Many people living with amyotrophic lateral sclerosis (PALS) report restrictions in their day-to-day communication (communicative participation). However, little is known about which speech features contribute to these restrictions. This study evaluated the effects of common speech symptoms in PALS (reduced overall speaking rate, slowed articulation rate, and increased pausing) on communicative participation restrictions. Participants completed surveys (the Communicative Participation Item Bank-short form; the self-entry version of the ALS Functional Rating Scale-Revised) and recorded themselves reading the Bamboo Passage aloud using a smartphone app. Rate and pause measures were extracted from the recordings. The association of various demographic, clinical, self-reported, and acoustic speech features with communicative participation was evaluated with bivariate correlations. The contribution of salient rate and pause measures to communicative participation was assessed using multiple linear regression. Fifty seven people living with ALS participated in the study (mean age = 61.1 years). Acoustic and self-report measures of speech and bulbar function were moderately to highly associated with communicative participation (Spearman rho coefficients ranged from rs = 0.48 to rs = 0.77). A regression model including participant age, sex, articulation rate, and percent pause time accounted for 57% of the variance of communicative participation ratings. Even though PALS with slowed articulation rate and increased pausing may convey their message clearly, these speech features predict communicative participation restrictions. The identification of quantitative speech features, such as articulation rate and percent pause time, is critical to facilitating early and targeted intervention and for monitoring bulbar decline in ALS.

Multiscale Scrutinizing Ion Storage Kinetics in Hollow Ni‐Mn Prussian Blue Analogues for Enhanced Capacitive Deionization

AbstractPrussian blue analogues (PBAs) are a class of promising materials for capacitive deionization. However, the kinetic mismatch between their slow ion storage rate and the demand from short‐time desalination severely limits their desalination performance. Here, a group of structure‐tuneable Ni‐Mn PBAs have been developed by a combination strategy of surface‐protected chemical etching and Ostwald ripening to study their ion storage kinetics. Treating them as demos, the characterizations and investigations, e.g., in situ XRD in a three‐electrode system, dynamic impedance, finite element simulation, and DFT calculations etc., reveal that the slow ion diffusion caused by the severe agglomeration of the nanoparticles and the unsuitable lattice parameter controls the final desalination behavior. Therefore, the correspondingly optimized sample (HC‐t) possessing a microscale hollow structure, nanoscale shell thickness, and expanded lattice, displays a fast ion storage kinetics with the ratio of surface‐controlled current as high as 82% at a scan rate of 20 mV s−1. Consequently, it delivers an impressive desalination capacity of 120.8 mg g−1 (2.06 mmol g−1 Na+) with a fast average desalination rate of 0.25 mg g−1 s−1 (0.004 mmol g−1 s−1) at 1.2 V, competitive with those reported in the literature. Moreover, the elucidation of the structure‐performance correlation provides valuable insights for the development and design of next‐generation PBAs for capacitive deionization (CDI).

Improved Lignin Conversion to High-Value Aromatic Monomers through Phase Junction CdS with Coexposed Hexagonal (100) and Cubic (220) Facets.

Photocatalysis has the potential for lignin valorization to generate functionalized aromatic monomers, but its application has been limited by the slow conversion rate and the low selectivity to desirable aromatic products. In this work, we designed the phase junction CdS with coexposed hexagonal (100) and cubic (220) facets to improve the photogenerated charge carriers' transfer efficiency from (100) facet to (220) facet and the hydrogen transfer efficiency for an enhanced conversion rate of lignin to aromatic monomers. Water is found as a sufficient external hydrogen supplier to increase the yields of aromatic monomers. These innovative designs in the reaction system promoted complete conversion of PP-ol to around 94% of aromatic monomers after 1 h of visible light irradiation, which shows the highest reaction rate and selectivity of target products in comparison with previous works. PP-one is a byproduct from the overoxidation of PP-ol and is usually difficult to be further cleaved to acetophenone and phenol as the desirable aromatic monomers. TEA was first identified in this study as a sacrificial electron donor, a hydrogen source, and a mediator to enhance the cleavage of the Cβ-O bonds in PP-one. With the assistance of TEA, PP-one can be completely cleaved to desirable aromatic monomer products, and the reaction time is reduced from several hours to 10 min of visible light irradiation.

Impact of Size and Distribution of k-Carbides on the Hydrogen Embrittlement and Trapping Behaviors of a Fe-Mn-Al-C Low-Density Steel.

This study compares the hydrogen embrittlement susceptibility of a Fe-30Mn-8Al-1.2C austenitic low-density steel aged at 600 °C for 0 (RX), 1 min (A1) and 60 min (A60), each exhibiting varying sizes and distributions of nano-sized κ-carbides. Slow strain rate tests were conducted to assess hydrogen embrittlement susceptibility, while thermal desorption analysis was applied to investigate hydrogen trapping behaviors. Fracture surface analysis was employed to discuss the associated failure mechanisms. The results suggest that nano-sized κ-carbides with sizes ranging from 2-4 nm play a crucial role in mitigating hydrogen embrittlement, contrasting with the exacerbating effect of coarse grain boundary κ-carbides. This highlights the significance of controlling the sizes and morphology of precipitates in designing hydrogen-resistant materials.

Migration behavior of iron and phosphorus during gas-based reduction for high-phosphorus iron ore

With the depletion of high-grade iron ore, it is necessary to develop low-quality high-phosphorus iron ore through economical and sustainable solutions. In this study, we presented simultaneous enrichment of iron (Fe) and phosphorus (P) to recover P from high-phosphorus iron ore and clarified the migration of P from the original apatite to reduced iron during the direct reduction process. To capture the migration route, gas-based reduction at a relatively slow rate was conducted on two typical iron ores samples (low-grade and high-grade) at different temperatures and times. Results indicate that there are concentration gradients for P and Fe of reaction products in the low-grade iron ore at 1400 °C. The P content continuously increased in the sequence from metallic iron (Fe), wustite (FeO), and fayalite (Fe2SiO4), to apatite (Ca3(PO4)3F). Conversely, the content of Fe gradually decreased. During this process, P dissolved from apatite entered and formed P-bearing fayalite. For the high-grade iron ore, P-bearing fayalite with a metastable structure disappeared as the reduction progressed, and P was released and then reduced to a gaseous state, finally absorbed by metallic iron. Furthermore, when metallic iron was not formed in the initial 60 min at 1300 °C, the P migrated from the apatite to the fayalite and gas phase. As the reduction time increased from 60 min to 240 min, the formed metallic iron provided a site for gasified P, which inhibited the volatilization of P and contributed to Fe and P enrichment.

Active Fabrics with Controllable Stiffness for Robotic Assistive Interfaces.

Assistive interfaces enable collaborative interactions between humans and robots. In contrast to traditional rigid devices, conformable fabrics with tunable mechanical properties have emerged as compelling alternatives. However, existing assistive fabrics actuated by fluidic or thermal stimuli struggle to adapt to complex body contours and are hindered by challenges such as large volumes after actuation and slow response rates. To overcome these limitations, we draw inspiration from biological protective organisms combining hard and soft phases, and propose active assistive fabrics consisting of architectured rigid tiles interconnected with flexible actuated fibers. Through programmable tessellation of target body shapes into architectured tiles and controlling their interactions by the actuated fibers, our active fabrics can rapidly (within seconds) transition between soft compliant configurations and rigid states conformable to the body (> 350 times stiffness change, loading capacity to weight ratio > 50) while minimizing the device volume after actuation. We demonstrate the versatility of our active fabrics as exosuits for tremor suppression and lifting assistance. We also present its potential as body armors for impact mitigation. Electrothermal actuators are integrated for smart actuation with convenient folding capabilities. Our work offers a practical framework for designing customizable active fabrics with shape adaptivity and controllable stiffness, these active fabrics have wide applications in wearable exosuits, haptic devices, and medical rehabilitation systems. This article is protected by copyright. All rights reserved.

Self Nanoelmusifying Drug Delivery System of Rosuvastatin: Bioavailability Evaluation and In vitro - In vivo Correlation.

Rosuvastatin, most commonly used in the form of calcium salt, belongs to the statin groups of synthetic antihyperlipidemic agents. Rosuvastatin possesses high permeability, however, its aqueous solubility is poor, causing a slow dissolution rate in water. Consequently, this dissolution rate has a decisive role in the release and absorption of rosuvastatin in the gastrointestinal tube. The aims of this study were to evaluate the absorption of the drug from the self-nano emulsifying drug delivery system of rosuvastatin (Ros SNEDDS) compared to rosuvastatin substance and to develop a level-A in vitro-in vivo correlation (IVIVC) for Ros SNEDDS. An in-house developed LC-MS/MS method was used to determine the concentrations of rosuvastatin in dog plasma. Six beagle dogs received an intravenous dose, Ros SNEDDS, rosuvastatin substance. In vitro dissolution of the Ros SNEDDS was carried out with different conditions. Correlation models were developed from the dissolution and absorption results of Ros SNEDDS. The results showed a 1.7-fold enhanced oral bioavailability and 2.1-time increase of rosuvastatin Cmax in Ros SNEDDS form, compared to the rosuvastatin substance. A 900 ml dissolution medium of pH of 6.6 has demonstrated its suitability, the in vitro dissolution model was studied and supported by the Weibull equation with a weighting factor of 1/y2 as it presented the lowest values of AIC. Ros SNEDDS demonstrated higher bioavailability of rosuvastatin in comparison to rosuvastatin substance and established a level A IVIVC used in future bioequivalence trials.

Accelerating cell division of Shewanella oneidensis to promote extracellular electron transfer rate for efficient pollution treatment

The slow rate of extracellular electron transfer (EET) of electroactive microorganisms (EAMs) remains a predominate bottleneck that restricts practical applications of bio-electrochemical systems. Cell division has significant effects on cell cycle, morphology, growth and metabolism. However, the relation between cell division and the EET rate of Shewanella oneidensis has not been established. Here, we employed modular engineering strategy to accelerate DNA replication in the C period and divisome formation in the D period of cell cycle, which decreased cellular volume and enhanced the EET efficiency. Assembly of the C and D period modules further decreased the cell volume by 82.0 % and enhanced power density by 3.12-fold. Electrophysiological and transcriptomic analyses synergistically revealed that the programmed cell volume decrease facilitated lactate uptake and cellular metabolism due to the increased specific surface area (SSA), which consequently reinforced intracellular electron generation. Moreover, the reduced cell size facilitated electroactive biofilm formation. Finally, programmed increase in riboflavin biosynthesis and transport further strengthened indirect EET and boosted output power density to 1537.8 ± 116.9 mW m−2, 21.1-fold of that of the WT. The engineered strains exhibited superior abilities for Cr6+ reduction and azo dyes degradation. This study shed light on the underlying mechanism how reduced cell size impacts electrophysiology of EAMs, and indicated accelerating cell division is a promising avenue to increase the EET of EAMs for efficient environmental pollution treatment.

Mechanism of Action of KL-50, a Candidate Imidazotetrazine for the Treatment of Drug-Resistant Brain Cancers.

Aberrant DNA repair is a hallmark of cancer, and many tumors display reduced DNA repair capacities that sensitize them to genotoxins. Here, we demonstrate that the differential DNA repair capacities of healthy and transformed tissue may be exploited to obtain highly selective chemotherapies. We show that the novel N3-(2-fluoroethyl)imidazotetrazine "KL-50" is a selective toxin toward tumors that lack the DNA repair protein O6-methylguanine-DNA-methyltransferase (MGMT), which reverses the formation of O6-alkylguanine lesions. We establish that KL-50 generates DNA interstrand cross-links (ICLs) by a multistep process comprising DNA alkylation to generate an O6-(2-fluoroethyl)guanine (O6FEtG) lesion, slow unimolecular displacement of fluoride to form an N1,O6-ethanoguanine (N1,O6EtG) intermediate, and ring-opening by the adjacent cytidine. The slow rate of N1,O6EtG formation allows healthy cells expressing MGMT to reverse the initial O6FEtG lesion before it evolves to N1,O6EtG, thereby suppressing the formation of toxic DNA-MGMT cross-links and reducing the amount of DNA ICLs generated in healthy cells. In contrast, O6-(2-chloroethyl)guanine lesions produced by agents such as lomustine and the N3-(2-chloroethyl)imidazotetrazine mitozolomide rapidly evolve to N1,O6EtG, resulting in the formation of DNA-MGMT cross-links and DNA ICLs in healthy tissue. These studies suggest that careful consideration of the rates of chemical DNA modification and biochemical DNA repair may lead to the identification of other tumor-specific genotoxic agents.

Exploration of Vitamin B6-Based Redox-Active Pyridinium Salts Towards the Application in Aqueous Organic Flow Batteries.

Pyridoxal hydrochloride, a vitamin B6 vitamer, was synthetically converted to a series of diverse redox-active benzoyl pyridinium salts. Cyclic voltammetry studies demonstrated redox reversibility under basic conditions, and two of the most promising salts were subjected to laboratory-scale flow battery tests involving galvanostatic cycling at 10 mM in 0.1 M NaOH. In these tests, the battery was charged completely, corresponding to the transfer of two electrons to the electrolyte, but no discharge was observed. Both CV analysis and electrochemical simulations confirmed that the redox wave observed in the experimental voltammograms corresponds to a two-electron process. To explain the irreversibility in the battery tests, we conducted bulk electrolysis with the benzoyl pyridinium salts, affording the corresponding benzylic secondary alcohols. Computational studies suggest that the reduction proceeds in three consecutive steps: first electron transfer (ET), then proton-coupled electron transfer (PCET) and finally proton transfer (PT) to give the secondary alcohol. 1H NMR deuterium exchange studies indicated that the last PT step is not reversible in 0.1 M NaOH, rendering the entire redox process irreversible. The apparent reversibility observed in CV at the basic media likely arises from the slow rate of the PT step at the timescale of the measurement.

Mapping the structural configuration of the northern part of the Central Indian Ridge from satellite gravity data using derivatives of the horizontal gradient

This study presents a novel approach to map the structural configuration of the northern part of the Central Indian Ridge from satellite-derived gravity data. The proposed approach is based on a combination of derivatives of the horizontal gradient of gravity anomalies. The robustness of the approach is tested on synthetic gravity examples before applying it to satellite gravity data of the northern part of the Central Indian Ridge. The results obtained from the synthetic examples show that the proposed method can map the structural boundaries more precisely and clearly compared to other techniques, and can avoid producing additional structures in output maps. For real application, the structural features determined from the proposed approach are consistent with the fracture zones that have been identified in the area. The obtained result reveals the prominent lineament trend is in the northeast-southwest direction, which is possibly related to plate movement during the Cenozoic. The result demonstrates a high lineament density that is in agreement with the slow spreading rate of the Central Indian Ridge. My findings also demonstrate that the proposed approach can be considered as a valuable tool in mapping structural boundaries.

Delayed fracture behavior of ultra-high-strength mooring chain steel evaluated by potentiostatic hydrogen-charging combined with SSRT

The influence of hydrogen charging potentials on the hydrogen embrittlement susceptibility of R6 ultra-high strength mooring chain steel was investigated via constant potential hydrogen charging slow strain rate tensile tests combined with thermal desorption analysis. The results reveal that hydrogen charging leads to a 38.94% decrease in elongation, while the impact on tensile strength is relatively minor. Furthermore, the specimens experienced intergranular cracking at the critical potential of −1150 mV, with the size of the brittle region increasing as the negative charging potential becomes more negative. And, hydrogen atoms can cause local embrittlement of materials and increase KAM value.

Synthesis and characterization of a dithiodiglycolic acid-incorporated poly(glycerol sebacate) exhibiting lipase resistance and antibacterial properties

Poly(glycerol sebacate) (PGS), a crosslinked network synthesized by polycondensation of glycerol and sebacic acid, has found successful utilization in various tissue engineering applications because of its biocompatibility, ease of synthesis, surface-erosion biodegradability, rubber-like elasticity, and adjustable mechanical properties. However, its fast in vivo degradation and lack of intrinsic antibacterial activity may be a concern for specific applications. The functional groups of glycerol and sebacic acid can react with those of other monomers, offering unlimited possibilities for generating new crosslinked networks tailored for particular purposes. Herein, we synthesized a series of poly(glycerol sebacate dithiodiglycolate) (PGSDTG) by incorporation of dithiodiglycolic acid (DTG) in the synthesis of PGS. PGSDTG exhibited reduced stiffness, sensitivity to glutathione (GSH), resistance to lipase degradation, and inhibition of bacterial adhesion and growth. The PGSDTG containing 45.6 wt% of DTG exhibited the lowest degradation rate with more than 80 wt% of PGSDTG remained at day 28 and the lowest bacterial inactivation rates of 99.2 ± 0.5 % and 82.5 ± 11.0 % against S. aureus and E. coli, respectively. This study suggested that PGSDTG may serve as a suitable antibacterial scaffold material for repairing or regenerating tissues characterized by a slow healing rate.

Anticipating the lifespan: Predicting the durability of an anode-supported solid oxide fuel cell short stack over 50,000 h

In the present study, the operational lifetime of a solid oxide fuel (SOFC) short stack is predicted by investigating the performance degradation of both the short stack and its cells throughout 1000 ​h at 800 ​°C. The short stack and integral cell voltages are continuously measured during the long-term test, with electrochemical impedance spectroscopy (EIS) conducted every 200 ​h. The short stack voltage decreased rapidly for the initial 200–300 ​h and afterwards, it decreased at a slow rate due to the increase in the Ohmic and polarization resistances in the same manner. Scanning electron microscopy results show that there is no delamination or cracking among constituent layers of the short-stack cells. The single degradation effects of the Ni coarsening in the anode, cation migration and surface segregation in cathode and oxide scale growth in metallic interconnect mesh are successfully integrated into a comprehensive lifetime prediction model. The experimentally measured voltage degradation data of the short stack fits well with the developed mathematical model and allows the successful prediction of the lifetime up to 50,000 ​h.

Drivers of organic carbon distribution and accumulation in the northern Barents Sea

Sedimentary properties and accumulation rates on the continental shelf and in the deep sea reflect temporal oceanographic, biological and chemical processes occurring in the water column and the sediment surface. We used the radionuclides 210Pb, 226Ra, and 137Cs activities to estimate sedimentation rates during the last century at nine stations in the northern Barents Sea region. Elemental (C, N) and stable isotopic composition (δ13C, δ15N) were also analysed from the nine stations sampled in August 2018, and, for five other stations sampled in August and December 2019, and in March and May 2021. Sediment accumulation rates varied between 130 and 1 410 g m−2 y−1. The < 63 μm normalized total organic carbon (TOC63) and the total nitrogen from the sediment surface varied between 0.90–2.56 % and 0.13–0.33 %, respectively. Ice-free shelf stations had higher TOC63 and possibly fresher organic matter (high δ13C, low δ15N) than ice-covered more northern stations. The opposite trend was observed for total inorganic carbon. We found that these trends in biogeochemical parameters were spatially structured by the winter sea ice concentration and biological production differences, and exhibited a south-north separation of the Polar Front region. The low and stable organic carbon accumulation rate (1.7–13.4 g Corg m-2 y−1; ARtoc) is a function of slow sedimentation rates, and high degradation and residence time in the water column and at the sediment–water interface. Overall, the ARtoc has been stable for the past 100 years, with a slight increase from the early 1970s to the present at the shelf and slope stations. Our results highlight that spatial scales of variability of the studied sedimentary parameters are linked to spatial patterns of important environmental variables (e.g., chlorophyll-a, sea ice concentration) in the region. In contrast, no seasonal differences were observed in the sediment parameters of revisited stations, and the dated sediment geochemical profiles did not exhibit substantial longer-term variation. This means that climate-induced changes in variables that modify the sedimentary geochemistry of the environment may affect benthic community activity and structure before leaving a record in ARtoc.

Role of Ti element in the microstructure and corrosion behavior of nickel-based alloy 825

The influence of Ti content on the microstructure and corrosion behavior of nickel-based alloy 825 in acid oil and gas environments was studied. The pitting corrosion behavior and stress corrosion cracking (SCC) behavior of Alloy 825 were investigated using high-temperature and high-pressure immersion tests, electrochemical tests, and slow strain rate tensile tests. Scanning electron microscopy, electron backscatter diffraction, and 3D microscopy were applied to analyze the microstructure and corrosion performance of the samples. The results showed that the number of inclusions and residual strain increased with the increase of Ti content, and strain concentration was found around the inclusions. The rise in inclusions led to lower pitting potential and a narrower passivation interval. In addition, the enhanced SCC susceptibility of the alloy with higher Ti content may also be attributed to the increase in inclusions.

EXTENSION CASE STUDY: WHY PADDY FARMERS ARE NOT INCLINED TO USE A DRONE AS PART OF MECHANISATION FOR PADDY CULTIVATION

Drone technology is emerging as a pivotal component in the agricultural sector, particularly in the context of Agricultural Industrial Revolution 4.0 (IR4.0). Its application, especially in activities such as fertiliser and crop protection chemical spraying in the Kemubu Agricultural Development Authority (KADA) granary areas, can significantly enhance the farmers’ yields. Despite the positive reception of drone technology, there is a growing phenomenon of technology rejection that requires further exploration. This research aims to investigate farmers’ acceptance of drones as a mechanisation tool for paddy cultivation in the Jajahan Bachok, Kelantan granary areas within KADA authority. A structured questionnaire, based on the knowledge, attitude, practice (KAP) model, was administered to 82 farmers surrounding Jajahan Bachok through purposive sampling. Data analysis using SPSS version 26.0 involved Descriptive statistics, Spearman’s Correlation, and Reliability tests. The study reveals that paddy farmers exhibit acceptance of drone technology, albeit with a slow adoption rate. The correlations between knowledge, attitude, and practice with drone mechanisation acceptance are significant but negligible at levels of 0.253, 0.866, and 0.69, respectively. This research is vital for both agency and drone vendors to comprehend the factors influencing drone technology acceptance among paddy farmers. Understanding these factors can contribute to enhance the application and adoption rate of drone as next important mechanisation for paddy farming activities among farmers especially in the KADA granary areas. Keywords: Drone, paddy, acceptance, KAP model, KADA.

Synthesis of polyaniline-doped magnetic iron foam photo catalyst (PANI@mIF) for integrated adsorptive photocatalytic degradation of nicosulfuron

ABSTRACT Nicosulfuron have low volatility and slow biodegradation rate, leading to its long persistency in soil and crops, which further upraised the risk of contamination of nearby water and severe damage to the crop rotation as may be its precursors are more harmful than nicosulfuron itself. In the present work, we performed a degradation study for the efficient removal of nicosulfuron from soil and water using Polyaniline-doped magnetic iron foam (PANI@mIF). The Photo catalyst was synthesised by doping of polyaniline on magnetic iron foam at 70°C and applied for the efficient photocatalytic degradation of nicosulfuron. PANI@mIF was then characterised through FTIR, SEM, EDX and XRD. The degradation of nicosulfuron was investigated under UV radiations and the resulted data were examined by fitting isotherms models. The Langmair model is well fitted to the adsorption data with R2 of 0.925, which demonstrates monolayer adsorption of nicosulfuron on the surface of PANI@mIF. The maximum adsorption capacity and percent degradation of 87% was achieved with PANI@mIF. Comparatively, good adsorption capacity of PANI@mIF is attributed to a large number of H bonding and electrostatic interactions. Kinetic study indicates the adsorption of nicosulfuron by PANI@mIF followed 2nd order kinetics with R2 of 0.958.The negative values of Gibbs free energy (−18294.3, 19543.1,-7530.4, −7307.7 and −7969.8), enthalpy (−1.97 × 10−4) and entropy (−3.54 × 10−3) indicate spontaneous and exothermic nature of the process. The reusable nature of PANI@mIF with 5 batches reflected its inventive photo catalytic behaviour for real sample applications and waste water treatment.