Intravascular Casting Radiopaque Hydrogel Systems for Transarterial Chemo/Cascade Catalytic/Embolization Therapy of Hepatocellular Carcinoma.

This paper introduces catheter-directed intravascular casting hydrogels for transarterial chemo/starvation/chemodynamic embolization (TACSCE) therapy of hepatocellular carcinoma (HCC). Comprising Mn ion-crosslinked hyaluronic acid-dopamine (HD) with glucose oxidase (for glucose decomposition to H2O2 in starvation therapy), doxorubicin (for chemotherapy), and iopamidol (for X-ray imaging), these hydrogels are fabricated for transarterial embolization therapy guided by X-ray fluoroscopy. Mn4+ (from MnO2) demonstrates strong coordination with the catechol group of HD, providing hypoxia relief through O2 generation and cellular glutathione (GSH) consumption, compared to the OH radical generation potential of Mn2+. The gelation time-controlled, catheter-injectable, and rheologically tuned multitherapeutic/embolic gel system effectively reaches distal arterioles, ensuring complete intravascular casting with fewer complications related to organic solvents. Glucose deprivation, cascade reactive oxygen species (ROS) generation, GSH depletion, and sustained release profiles of multiple drug cargos from the hydrogel system are also achieved. The combined chemo/starvation/chemodynamic efficacies of these designed hydrogel systems are confirmed in HCC cell cultures and HCC-bearing animal models. The developed radiopaque/injectable/embolic/sol-to-gel transformable systems for TACSCE therapy may offer enhanced therapeutic efficacies compared to typical transarterial embolization and transarterial chemoembolization procedures for HCC.

One-pot synthesis of sodium alginate-grafted-terpolymer hydrogel for As(III) and V(V) removal: In situ anchored comonomer and DFT studies on structures.

In this work, an optimum sodium alginate (NaAlg)-grafted-[sodium 2-methylenesuccinate-co-sodium 2-((2-(isobutyryloxy)ethoxy)methyl)succinate-co-ethylene glycol methacrylate, i.e., SMS-co-SIBEMS-co-EGMA, i.e., P1], i.e., P2, was selected among twelve hydrogels synthesized by employing variable amounts of synthesis parameters through a facile polymerization of SMS and EGMA monomers. In P1 and P2, SIBEMS third comonomer was strategically anchored in situ. The formation of terpolymer, i.e., P1, rather than generally expected copolymer, i.e., SMS-co-EGMA/ CoP1, was explored via closeness of experimental and simulated excitation energies of P1 and CoP1, measured by using density functional theory (DFT). The grafting of NaAlg into synthetic P1 elevated swelling, crosslink density (CD), network stability, reusability, and adsorption capacity (AC) of semisynthetic hydrogel, i.e., P2. The reusable P2 presenting optimum result among swelling, CD, and mean molar mass was chosen selectively for removals of As(III) and V(V). The structures of P1, P2, and adsorbed P2, i.e., As(III)-P2 and V(V)-P2; NaAlg-grafting; in situ anchored SIBEMS comonomer; reusability; thermostability; and surface properties were explored through XPS-NMR-FTIR-UV-vis, DFT, TG, DLS, XRD, SEM, pHPZC, and network and thermodynamic energies. The ACs of 0.025 g P2 for As(III) and V(V) were 112.24 and 88.89 mg g-1, respectively, at 308 K and within 5-100 mg L-1. The ACs reduced to 67.26, 75.49, 71.42, and 98.25 mg g-1 for As(III) and 40.25, 50.49, 45.37, and 67.88 mg g-1 for V(V) in the presence of Mn(II), Cu(II), Ni(II), and Zn(II), respectively.

Chitosan-grafted tetrapolymer using two monomers: pH-responsive high-performance removals of Cu(II), Cd(II), Pb(II), dichromate, and biphosphate and analyses of adsorbed microstructures.

For circumventing the cumbersome and expensive multifunctional and multipolymer adsorbents for high-performance removals of hazardous water-contaminant(s), chitosan-g-[2-acrylamido-2-methyl-1-propanoic acid (AMPS)-co-2-(3-acrylamidopropanamido)-2-methylpropane-1-sulfonic acid (APAMPS)-co-2-(N-(3-amino-3-oxopropyl)acrylamido)-2-methylpropane-1-sulfonic acid (NAOPAMPS)-co-acrylamide (AM)] (i.e., chitosan-g-tetrapolymer), a multifunctional scalable and reusable hydrogel, was synthesized by grafting of chitosan and in situ attachments of N-H functionalized NAOPAMPS and APAMPS hydrophilic acrylamido-monomers during free-radical solution-polymerization of the two ex situ added AMPS and AM monomers in water. The response surface methodology was employed to synthesize one hydrogel envisaging the optimum balance between swelling and stability for the superadsorption of Cu(II), Cd(II), Pb(II), Cr2O72-, and HPO42-. The in situ attachments of NAOPAMPS and APAMPS, grafting of chitosan into tetrapolymer, structures and properties, pH-responsive abilities, superadsorption mechanism, and reusability were understood via in depth microstructural analyses of adsorbed and/or unadsorbed chitosan-g-tetrapolymer(s) through 1H/13C NMR, FTIR, XPS, TGA, XRD, DLS, and pHPZC. The maximum adsorption capacities of Cd(II), Cu(II), Pb(II), Cr2O72-, and HPO42- were 1374.41, 1521.08, 1554.08, 47.76, and 32.76 mg g-1, respectively.

Changes in plantar load distribution and gait pattern following foot drop correction in leprosy affected patients.

This study was done to compare the changes in plantar load (weight distribution) and gait patterns before and after tibialis posterior transfer surgery in people affected by leprosy. Changes in gait patterns were observed and proportionate changes in plantar load were quantified using data captured by a baropodometer. All the eight patients who underwent tibialis posterior transfer surgery in 2013 in our hospital were included in the study. In addition to the regular pre-operative and post-operative assessments, the patients also underwent baropodometric evaluation. There was a significant change in plantar load at the heel, lateral border and forefoot. Using the foot pressure scan, it was noted that the progression of the centre of mass (displayed graphically as 'the gait line') was also affected by the altered pattern of weight distribution. This study reiterates the importance of tibialis posterior transfer because: it restores the normal gait pattern of 1, 2, 3 (where 1 is heel strike, 2 is mid foot contact and 3 is forefoot contact) and provides a more uniform distribution of planter load.

pH-Responsive Biocompatible Fluorescent Hydrogel for Selective Sensing and Adsorptive Recovery of Dysprosium.

The elevated accumulation of electronic wastes, especially containing Dysprosium ion [i.e., Dy(III)], is emerging as a potential environmental threat. To overcome the deleterious effects of Dy(III), detection and removal of Dy(III) is crucial. Moreover, recovery of high-value Dy(III) is economically beneficial. However, the availability of a single material, capable of sensing Dy(III) in nanomolar concentration and simultaneously adsorbing it with high adsorption capacity (AC), is rare. Therefore, to solve this problem, a pH-responsive fluorescent amino graphene oxide-impregnated-engineered polymer hydrogel (AGO-EPH) has been synthesized, suitable for selective sensing of Dy(III) in nanomolar concentration and adsorbing it from wastewater at ambient temperature. This terpolymeric hydrogel is synthesized from two nonfluorescent monomers, propenoic acid (PNA) and prop-2-enamide (PEAM), along with an in situ generated comonomer (3-acrylamidopropanoic acid/AAPPA) through N-H activation during polymerization. Surface properties and structural details of AGO-EPH are established using NMR, FTIR, XRD, TEM, SEM, EDX, Raman, MALDI-mass, and DLS studies. The AGO-EPH exhibits blue fluorescence with selective turn-off sensing of Dy(III) with the detection limit of 1.88 × 10-7 (M). The maximum AC of AGO-EPH is 41.97 ± 0.39 mg g-1. The developed AGO-EPH shows consistent adsorption-desorption property over five cycles, with more than 90% desorption efficiency per cycle, confirming significant recovery of the valuable Dy(III). From Logic gate calculations, complexation of Dy(III) and AGO-EPH may be the reason behind fluorescence quenching. The AGO-EPH also shows antibacterial action against ∼3 × 108 cells mL-1 of E. coli solution. Overall, the developed pH-responsive engineered hydrogel can be used as a potential low-cost sensing device and reusable adsorbent for Dy(III).

Ligand-selective turn-off sensing, harvesting and post-adsorptive use of Dy(III) and Yb(III) by intrinsically fluorescent flower-shaped Gum Acacia-grafted hydrogels.

Rare earth metals (REMs), such as Dysprosium (Dy) and Ytterbium (Yb), have experienced unprecedented demand in recent times due to their applications in high-end technologies. REMs are found only in select geographic locations placing tremendous economic constraints on their use. In this work, we have developed Gum Acacia-grafted hydrogels (GmAc-FluoroTerPs) that are capable of selective detection and capture of Dy and Yb. The intrinsically blue fluorescent polymer hydrogel GmAc-FluoroTerP has been optimized for Dy(III) and Yb(III) specific quenching, enabling limit of detection of the REMs at 0.13 nM and 60.8 pM, respectively. A comprehensive structural characterization of the fluorescent hydrogel has been performed via NMR, FTIR, XPS, EPR, TGA, XRD, TEM, SEM, EDX, TCSPC, and DLS. In addition to an in situ generated fluorophore, GmAc-FluoroTerP displays a distinctive aggregation induced emission enhancement in mixed solvents. The complexation of Dy(III)/Yb(III) with GmAc-FluoroTerP hydrogel has been characterized by XPS, TCSPC, and logic gate analyses, and the adsorptive capacity for Dy(III) and Yb(III) are found to be best reported till date as 125.57 mg g-1 and 102.27 mg g-1, respectively. Desorption at acidic pH allows recovery of the REMs. We also report semiconducting behaviour of the native fluorescent hydrogel, that is enhanced upon adsorptive capture of Dy(III) and Yb(III), with calculated band gaps at 1.37, 0.77, and 0.49 eV, respectively. The convergent sensing, capture, and reuse of Dy(III) and Yb(III) presented in this work promises a hitherto unreported template for application on other REMs.

Hydrogel design to overcome thermal resistance and ROS detoxification in photothermal and photodynamic therapy of cancer.

Responsive heat resistance (by heat shock protein upregulation) and spontaneous reactive oxygen species (ROS) detoxification have been regarded as the major obstacles for photothermal/photodynamic therapy of cancer. To overcome the thermal resistance and improve ROS susceptibility in breast cancer therapy, Au ion-crosslinked hydrogels including indocyanine green (ICG) and polyphenol are devised. Au ion has been introduced for gel crosslinking (by catechol-Au3+ coordination), cellular glutathione depletion, and O2 production from cellular H2O2. ICG can generate singlet oxygen from O2 (for photodynamic therapy) and induce hyperthermia (for photothermal therapy) under the near-infrared laser exposure. (-)-Epigallocatechin gallate downregulates heat shock protein to overcome heat resistance during hyperthermia and exerts multiple anticancer functions in spite of its ironical antioxidant features. Those molecules are concinnously engaged in the hydrogel structure to offer fast gel transformation, syringe injection, self-restoration, and rheological tuning for augmented photo/chemotherapy of cancer. Intratumoral injection of multifunctional hydrogel efficiently suppressed the growth of primary breast cancer and completely eliminated the residual tumor mass. Proposed hydrogel system can be applied to tumor size reduction prior to surgery of breast cancer and the complete remission after its surgery.

An MXene-Grafted Terpolymer Hydrogel for Adsorptive Immobilization of Toxic Pb(II) and Post-Adsorption Application of Metal Ion Hydrogel.

Toxic metal ions present in industrial waste, such as Pb(II), introduce deleterious effects on the environment. Though the adsorptive removal of Pb(II) is widely reported, there is a dearth of research on the suitable utilization and disposal of the Pb(II)-adsorbed adsorbent. In this work, an MXene-grafted terpolymer (MXTP) hydrogel has been designed for the adsorption of Pb(II) under ambient conditions of pH and temperature. The hydrogel MXTP was synthesized by facile one-pot polymerization in aqueous solvent, and the detailed structural characterization of terpolymer (TP), MXTP, and Pb(II)-loaded MXTP, i.e., Pb(II)-MXTP, was carried out by a combination of proton nuclear magnetic resonance (1H NMR), Fourier-transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffractometric (XRD), thermogravimetric/differential thermogravimetric (TG/ DTG), and field emission scanning electron microscopic (FESEM) analyses. The specific capacitance and conductivities of Pb(II)-MXTP were studied with cyclic voltammetry (CV) and electrical impedance spectroscopy (EIS), which unambiguously indicate successful post-adsorption application. The specific capacitance of MXTP decreased after Pb(II) adsorption, whereas the conductivity increased significantly after Pb(II) adsorption, showing that MXTP can be successfully deployed as a solid electrolyte/anode after Pb(II) adsorption. This study covers the synthesis of a novel MXene-grafted terpolymer hydrogel for adsorptive exclusion of Pb(II) and assessment of the as-adsorbed Pb(II)-loaded hydrogel as a solid electrolyte/anode material and is the first demonstration of such post-adsorptive application.

Alum-tuned hyaluronic acid-based hydrogel with immune checkpoint inhibition for immunophoto therapy of cancer.

Alum-crosslinked hyaluronic acid-dopamine (HD) hydrogel containing indocyanine green (ICG) with anti-programmed cell death-1 (PD-1) antibody (Ab) administration was developed for immunophoto therapy of cancer. Alum modulates the rheological characteristics of hydrogel for enabling syringe injection, shear-thinning feature, and slower biodegradation. In addition, alum in HD-based hydrogel provided CD8+ T cell-mediated immune responses for cancer therapy. ICG in the hydrogel under near-infrared (NIR) light exposure may induce hyperthermia and generate singlet oxygen for selective cancer cell killing. HD/alum/ICG hydrogel injection with NIR laser irradiation elevated PD-1 level in CD8+ T cells. Administration of PD-1 Ab aiming at highly expressed PD-1 in T cells may amplify the anticancer efficacies of HD/alum/ICG hydrogel along with NIR laser. HD/alum/ICG hydrogel with NIR light may have both CD8+ T cell-linked immune responses and ICG-related photodynamic/photothermal effects. Additional injection of immune checkpoint inhibitor can ultimately suppress primary and distant tumor growth by combination with those therapeutic actions.

Manganese Sulfate Nanocomposites Fabricated by Hot-Melt Extrusion for Chemodynamic Therapy of Colorectal Cancer.

The development of metal salts-based nanocomposites is highly desired for the Fenton or Fenton-like reaction-based chemodynamic therapy of cancer. Manganese sulfate (MnSO4)-dispersed nanoparticles (NPs) were fabricated with a hot-melt extrusion (HME) system for the chemodynamic therapy of colorectal cancer in this study. MnSO4 was homogeneously distributed in polyethylene glycol (PEG) 6000 (as a hydrophilic polymer) with the aid of surfactants (Span 80 and Tween 80) by HME processing. Nano-size distribution was achieved after dispersing the pulverized extrudate of MnSO4-based composite in the aqueous media. The distribution of MnSO4 in HME extrudate and the interactions between MnSO4 and pharmaceutical additives were elucidated by Fourier-transform infrared, X-ray diffractometry, X-ray photoelectron spectroscopy, and scanning electron microscopy analyses. Hydroxyl radical generation efficiency by the Fenton-like chemistry capability of Mn2+ ion was also confirmed by catalytic assays. By using the intrinsic H2O2 in cancer cells, MnSO4 NPs provided an elevated cellular reactive oxygen species level, apoptosis induction capability, and antiproliferation efficiency. The designed HME-processed MnSO4 formulation can be efficiently used for the chemodynamic therapy of colorectal cancer.

Synthesis of gum tragacanth-grafted pentapolymer hydrogels for As(III) exclusion: Roles of microwaves, RSM optimization, and DFT studies.

Microwave assisted homogeneous heating, selectivity in radical formation, and the faster polymerization facilitate the synthesis, structures, properties, and the higher branching associated stability of multifunctional multipolymers. Thus, the optimum gum tragacanth (GMTR)-grafted pentapolymer hydrogel/ HG2 was synthesized from three monomers, i.e., cis-butenedioic acid (cBDA), N-hydroxymethylacryalamide (NHMAm), and 2-(methacryloyloxy)ethanol (MAOE), and in situ generated 2-(3-((hydroxymethyl)amino)-3-oxopropoxy)ethyl-2-methylbutanoate (CM1) and 2-hydroxyethyl 3-(N-(hydroxymethyl)-2-methylbutanamido)-2-methylpropanoate (CM2) comonomers through microwave assisted facile polymerization in aqueous medium. Here, twenty-one GMTR-grafted-[cBDA-co-CM1-co-NHMAm-co-CM2-co-MAOE/ HG1] hydrogels were prepared by using variable amounts of synthesis parameters, of which the optimum HG2 was chosen for the scale-up repetitive As(III)-exclusion. RSM was used to measure the optimum power-temperature-time of microwave irradiation. The structures of HG1, HG2, and As(III)-adsorbed HG2/ As(III)-HG2, in situ anchored comonomers, GMTR-grafting, reusability, thermostability, and surface phenomena were comprehended by XPS, NMR, UV-vis, FTIR, TG, XRD, DLS, and SEM analyses; pHPZC; network parameters; and thermodynamic variables. The geometries, electronic structures, and variable coordinations of As(III) with HG2 were investigated through DFT studies of HG2 and As(OH)3-HG2. The highest exclusion efficiency of 25 mg HG2 within 5-100 mg L-1 As(III) and at 298 K was 192.91 mg g-1, which was significantly higher than that of HG1.

Scale-up one-pot synthesis of waste collagen and apple pomace pectin incorporated pentapolymer biocomposites: Roles of waste collagen for elevations of properties and unary/ ternary removals of Ti(IV), As(V), and V(V).

Herein, hazardous solid particulate waste collagenic fibers (SWCFs) of leather industries were incorporated into apple pomace pectin (APPN)-grafted-pentapolymer, i.e., APPN-g-[sodium 2-methylidenebutanedioate(SMBD)-co-N-((3-(isopropylamino)-3-oxopropoxy) methyl) butyramide (CM1)-co-N-(hydroxymethyl)prop-2-enamide (NHMPE)-co-N-(hydroxymethyl)-4-(N-isopropylbutyramido)butanamide (CM2)-co-N-(propan-2-yl)prop-2-enamide NPYPE)/ PENP1], i.e., APPN-g-PENP1/ PENP2, prepared via one-pot facile polymerization of APPN and synthetic monomers, i.e., SMBD, NHMPE, and NPYPE, in aqueous medium, to fabricate an optimum multifunctional hybrid biocomposite adsorbent/ HCOM3. In PENP1, PENP2, and HCOM3, fourth/ CM1 and fifth/ CM2 multifunctional comonomers were anchored in situ. The structures of PENP1, PENP2, HCOM3, CM1, CM2, and metal-ion adsorbed HCOM3; APPN-grafting; SWCF incorporation; and surface properties were analyzed through NMR, XPS, FTIR, XRD, and SEM. The elevated adsorption efficiencies (AEs), reusability, thermostability, swelling, network durability, and crosslink density of HCOM3 were attributed to variable functionalities of SWCF/ APPN, explored by DLS and TGA, swelling, network, and thermodynamic parameters. Compared to SWCF, APPN, PENP1, and PENP2, the elevated AEs and reusability compelled HCOM3 as more suitable for scalable waste management. The maximum AEs, i.e., 171.79, 180.47, and 177.27 mg g-1, for Ti(IV), As(V), and V(V) at pHop = 7.0, 3.0, and 5.0, respectively, within 5-100 mg L-1 and at 298 K for 25 mg HCOM3 deteriorated during ternary adsorption by the antagonistic effects.

New property-performance optimization of scalable alginate-g-terpolymer for Ce(IV), Mo(VI), and W(VI) exclusions.

New property-performance optimization approach of purely-aliphatic scalable-and-reusable multifunctional terpolymer hydrogels envisaging the excellent performance potential has been reported. Accordingly, the optimum potassium alginate (KA)-g-[2-hydroxyethylmethacrylate (HEMA)-co-3-(2-(isobutyryloxy)ethoxy)-2-methylpropanoic acid (IBEMPA)-co-methacrylic acid (MAA)/ 1], i.e., 2, among twelve KA-grafted terpolymer hydrogels has been designed and synthesized via OH functionalized OC/ CC coupled in situ protrusion of third monomer, i.e., IBEMPA, and grafting of KA into 1 in polymerization of two monomers employing variable monomer ratio; pH; amounts of KA, crosslinker, and initiators; and temperatures. The structures of 1/ 2, in situ IBEMPA, grafted-KA, thermal stabilities, surface properties, superadsorption mechanism, and reusability have been explored via 1H/ 13C NMR, FTIR, XPS, TGA, XRD, SEM, DLS, network parameters, pHPZC, %graft-ratio, %gel-content, and thermodynamic-parameters. The maximum adsorption capacities of Ce(IV), Mo(VI), and W(VI) are 1575.57, 1581.32, and 1990.11 mg g-1, respectively, within 500-1000 ppm at 308 K for 0.02 g adsorbent.

Intrinsically Fluorescent Biocompatible Terpolymers for Detection and Removal of Bi(III) and Cell Imaging.

Intrinsically fluorescent biocompatible multifunctional multipurpose terpolymers, i.e., methyl methacrylate-co-methyl 3-(N-isopropylacrylamido)-2-methylpropanoate-co-N-isopropylacrylamide (MMA-co-MNIPAMP-co-NIPAm, 1) and methyl methacrylate-co-methyl 3-(N-hydroxymethylacrylamido)-2-methylpropanoate-co-N-hydroxymethylacrylamide (MMA-co-MNHMAMP-co-NHMAm, 2), were synthesized via in situ-attached acrylamido-ester monomers during polymerization of hydrophobic monomers in water medium. These nonconjugated fluorescent terpolymers presenting aggregation-enhanced emissions (AEEs) were suitable for Bi(III) sensors, Bi(III) removal, cell imaging, and security inks. The fluorescence properties, mechanisms of quenching, interactions of Bi(III) with 1 and 2, and Bi(III) adsorption were explored using theoretical analyses of 1, 2, Bi(III)-1, and Bi(III)-2. Considering the overall properties, 1 was more suitable for diverse prospective applications.

Starch-g-tetrapolymer hydrogel via in situ attached monomers for removals of Bi(III) and/or Hg(II) and dye(s): RSM-based optimization.

Response surface methodology (i.e., RSM)-optimized starch-g-[2-acrylamido-2-methylpropane sulfonic acid (AMPS)-co-[2-(N-(3-(hydroxymethyl)amino)-3-oxopropyl)acrylamido)-2-methylpropane sulfonic acid] (NHMAOAMPS)-co-[2-(3-(N-(hydroxymethyl)acrylamido)propanamido)-2-methylpropane sulfonic acid (NHMAPMPS)]-co-N-(hydroxymethyl)acrylamide (NHMA)] (i.e., starch-g-tetrapolymer) was synthesized via grafting of starch and in situ strategic protrusion of NHMAOAMPS and NHMAPMPS, using optimum ingredients and temperature. This interpenetrating tetrapolymer-hydrogel bearing extraordinary physicochemical properties and recyclability was applied for unary and/or binary removal(s) of Bi(III)-Hg(II) and brilliant green-crystal violet. The N-H-activated in situ allocation of monomers, grafting of starch, thermal stabilities, surface properties, swellability, sustainability, adsorption capacities, and superadsorption were apprehended via microstructural analyses of unadsorbed and/or adsorbed starch-g-tetrapolymer(s) through FTIR-1H-/13C-NMR-UV-vis, TGA-DSC, XRD, SEM-EDX, DLS, and %gel-content-pHPZC-%graft-ratio. The chemisorption data for metal ions best fitted with Langmuir and combined Langmuir-Freundlich isotherm models for unary and binary adsorption, respectively. The unary/binary adsorption capacities were 1005.41/959.25 and 1087.79/758.56 mg g-1 for Bi(III) and Hg(II), respectively, at 293 K, 0.02 g, and within 500-1000 ppm.

Pectin-grafted terpolymer superadsorbent via N-H activated strategic protrusion of monomer for removals of Cd(II), Hg(II), and Pb(II).

Pectin (PC)-g-[methacrylic acid (MAA)-co-3-(N-isopropylacrylamido)-2-methylpropanoic acid (NIPAMPA)-co-N-isopropylacrylamide (NIPA)] (i.e., PC-g-TP), a novel interpenetrating terpolymer network hydrogel of excellent physicochemical properties and reusability, was synthesized via grafting of PC and in situ strategic protrusion of third monomer, i.e., NIPAMPA, during polymerization of MAA and NIPA, using response surface methodology optimized amounts of ingredients and temperature, for superadsorption of hazardous metal ions, such as Cd(II), Hg(II), and Pb(II). The in situ allocation of NIPAMPA via NH activation, grafting of PC into MAA-co-NIPAMPA-co-NIPA matrix, physicochemical properties, and superadsorption mechanism were rationalized via extensive microstructural analyses of unadsorbed and/or adsorbed PC-g-TP through 1H-/13C-NMR, XPS, FTIR,TGA, XRD, FESEM, DLS, %gel content, pHPZC, and %graft ratio. The spontaneous chemisorption data exhibited excellent fitting with Langmuir model. The adsorption capacities (ACs) were 1315.32, 1172.97, and 1269.09 mg g-1 for Cd(II), Hg(II), and Pb(II), respectively, at 293 K, 0.02 g of PC-g-TP, and within 500-1000 ppm.

Collagenic waste and rubber based resin-cured biocomposite adsorbent for high-performance removal(s) of Hg(II), safranine, and brilliant cresyl blue: A cost-friendly waste management approach.

Goat buffing dust (GBD), an abundantly available collagenic-waste and crosslinked styrene butadiene rubber (SBR)-based scalable biocomposite showing excellent physicochemical properties and reusability was synthesized via systematic optimization of torque and time for exclusion(s) of dyes, such as safranine (SF) and brilliant cresyl blue (BCB), and Hg(II). The GBD-aided non-sulfur curing of SBR was attempted via chromane mechanism-based reaction between resin components of GBD and pendant ̶ C=C ̶ of SBR. The decrease in the relative extent of unsaturation in cured-SBRGBD, alteration of crystallinity, surface properties, elevated thermal stabilities, and ligand-selective superadsorption were inferred through extensive microstructural analyses of unadsorbed and/or adsorbed SBRGBD using 13C NMR, O1s-/N1s-/C1s-/Hg4f7/2,5/2-XPS, FTIR, UV-vis, TGA, XRD, FESEM, and EDX. Interactive effects between pHi, temperature, and concentration on adsorption capacities (ACs) were optimized through response surface methodology (RSM). The ionic interaction between SBRGBD and SF, BCB, and Hg(II) was understood through FTIR analyses, fitting of kinetics data to pseudosecond order model, and activation energies. BET and Langmuir isotherms were fitted the best to BCB and SF/Hg(II), respectively. Thermodynamically spontaneous chemisorption showed the maximum ACs of 165.63, 251.18, and 225.56 mg g-1 for SF, BCB, and Hg(II), respectively, at 100 ppm, 303 K, and adsorbent dose = 0.015 g.

Carbohydrate and collagen-based doubly-grafted interpenetrating terpolymer hydrogel via N-H activated in situ allocation of monomer for superadsorption of Pb(II), Hg(II), dyes, vitamin-C, and p-nitrophenol.

Herein, guar gum (GG)-g-(acrylic acid (AA)-co-3-acrylamido propanoic acid (AMPA)-co-acrylamide (AM))-g-cow buffing dust (CBD)/(GGTPCBD), a smart carbohydrate and protein-based doubly-grafted interpenetrating terpolymer hydrogel showing excellent physicochemical properties and recyclability was synthesized by in situ strategic allocation of AMPA during solution polymerization of AA and AM through systematic optimization of the amounts of components and reaction temperature for superadsorption of Hg(II), Pb(II), methyl violet (MV), methylene blue (MB), p-nitrophenol (PNP), and vitamin-C (vit.C). The in situ strategic protrusion of AMPA, grafting of both GG and CBD into AA-co-AMPA-co-AM, and ligand-selective superadsorption was inferred by advanced microstructural analyses of unadsorbed- and/or adsorbed-GGTPCBD using FTIR, 1H/13C NMR, O1s-/N1s-/C1s-/Pb4f7/2,5/2-/Hg4f7/2,5/2-XPS, UV-vis, TGA, DSC, XRD, DLS, SEM, EDX, % gel content, % -COOH, and pHPZC. The prevalence of covalent, ionic, and variegated interactions was rationalized by FTIR, fitting of kinetics data to the pseudosecond order model, and activation energies of adsorption. The BET and Langmuir isotherms fitted the best to MB and Hg(II)/Pb(II)/MV, respectively. Thermodynamically spontaneous chemisorption processes showed the maximum adsorption capacities (ACs) of 976.64, 859.23, 116.80, and 58.52 mg g-1 for Pb(II), Hg(II), MV, and MB, respectively, at 303 K, adsorbent dose = 0.01 g, and initial concentration of metal ions/dyes = 800/30 ppm.

Structures, Properties, and Performances-Relationships of Polymeric Membranes for Pervaporative Desalination.

For the fulfilment of increasing global demand and associated challenges related to the supply of clean-and-safe water, PV has been considered as one of the most attractive and promising areas in desalinating salty-water of varied salinities. In pervaporative desalination, the sustainability, endurance, and structural features of membrane, along with operating parameters, play the dominant roles and impart paramount impact in governing the overall PV efficiency. Indeed, polymeric- and organic-membranes suffer from several drawbacks, including inferior structural stability and durability, whereas the fabrication of purely inorganic membranes is complicated and costly. Therefore, recent development on the high-performance and cost-friendly PV membrane is mostly concentrated on synthesizing composite- and NCP-membranes possessing the advantages of both organic- and inorganic-membranes. This review reflects the insights into the physicochemical properties and fabrication approaches of different classes of PV membranes, especially composite- and NCP-membranes. The mass transport mechanisms interrelated to the specialized structural features have been discussed. Additionally, the performance potential and application prospects of these membranes in a wide spectrum of desalination and wastewater treatment have been elaborated. Finally, the challenges and future perspectives have been identified in developing and scaling up different high-performance membranes suitable for broader commercial applications.

Guar Gum-Grafted Terpolymer Hydrogels for Ligand-Selective Individual and Synergistic Adsorption: Effect of Comonomer Composition.

Grafting of guar gum (GG) and in situ strategic attachment of acrylamidosodiumpropanoate (ASP) via solution polymerization of acrylamide (AM) and sodium acrylate (SA) resulted in the synthesis of a sustainable GG-g-(AM-co-SA-co-ASP)/GGAMSAASP interpenetrating polymer network (IPN)-based smart superadsorbent with excellent physicochemical properties and reusability, through systematic optimization by response surface methodology (RSM) for removal of methyl violet (MV) and/or Hg(II). The relative effects of SA/AM ratios, in situ allocation of ASP, grafting of GG into the AMSAASP terpolymer, ligand-selective superadsorption mechanism, and relative microstructural changes in individually/synergistically-adsorbed MV-/Hg(II)-/Hg(II)-MV-GGAMSAASPs were determined by extensive analyses using Fourier transform infrared (FTIR), proton nuclear magnetic resonance, ultraviolet-visible (UV-vis), and O 1s-/N 1s-/C 1s-/Hg 4f7/2,5/2-X-ray photoelectron spectroscopies, thermogravimetric analysis, differential scanning calorimetry, X-ray diffraction, field emission scanning electron microscopy, and energy-dispersive spectroscopy and were supported by % gel content, pHPZC, and % graft ratio. The ionic/covalent-bonding, monodentate, bidentate bridging, and bidentate chelating coordination between GGAMSAASPs and Hg(II), and MV+-Hg(II) bonding were rationalized by FTIR, UV-vis, fitment of kinetics data to the pseudo-second-order model, and thermodynamic parameters. The maximum adsorption capacities of 49.12 and 53.28 mg g-1 were determined for Hg(II) and MV, respectively, under optimized conditions.