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The plant mediated biogenic synthesis of nanoparticles is of magnificent concern due to its eco-benign and single pot nature. Here, Cinnamomum tamala (C. tamala) aqueous leaf extract was utilised for the silver nanoparticles’ (Ag NPs) synthesis. The phytoconstituents in the leaf extract were analysed by standard methods. These metabolites, especially carbohydrate polymers reduce Ag ions to Ag NPs accompanied by a reddish-brown coloration of the reaction mixture. The visual observation of intense brown colour is the first indication of the formation of Ag NPs. Various spectro-analytical techniques further characterise the Ag NPs. The green synthesised spherical Ag NPs were crystalline with an average size of 38 nm. The Ag NPs were scrutinised for antioxidant, antimicrobial and cytotoxic activity and obtained good results. The free radical scavenging was studied by 2, 2-Diphenyl-l-picrylhydrazyl (DPPH) assay. The antibacterial activity of Ag NPs was assessed against human pathogens, and it shown to have good antibacterial potency against a wide spectrum of bacteria. The cytotoxic activity against HEK-293T (human embryonic kidney) cell line was evaluated by 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) assay. These potent biological activities enable C. tamala capped Ag NPs to be suitable candidates for the future applications in various fields, predominantly clinical and biomedical.

In this study, nanoiron and nanoiron+Au particles were synthesised using aqueous Aegle marmelos extract using a facile and one-pot approach. Lower size non-magnetic nanoiron (~34 nm) and nanoiron (~34 nm) +Au particles (1 to 1.5 µm) were produced from the same medium individually. Nanoparticles suspension behaviour and structural characterisations were carried out by UV-Vis spectroscopy, electron microscopy and by X-ray diffraction techniques. Primarily, for synthesis, a simple bioreduction approach generated amorphous nanoiron particles, which on annealing produced magnetic maghemite, γ-Fe2O3 type nanoparticles with sizes 100 to 1000 nm. Posteriorly, the bioreduction process also produces nanoiron+Au particles and can be used for multifunctional applications. As a model application, catalytic application of the as-prepared nanoiron and nanoiron+Au particles towards methylene blue, a thiazine dye degradation is investigated and found to be effective within 20 min. Langmuir-Hinshelwood kinetic model was exploited to know the degradation behaviour, and the model was found to be fit based on R 2 values with the observed experimental data. We suggest that the formed highly stable nanoiron particles with in situ stabilisation offer benefits like consistency, environmental friendliness and suits well for large-scale applicability.

This review summarizes and broadly classifies all of the major sustainable natural carbohydrate bio-macromolecular manifestations in nature - from botanical (cellulose, starch, and pectin), seaweed (alginate, carrageenan, and agar), microbial (bacterial cellulose, dextran, and pullulan), and animal (hyaluronan, heparin, chitin, and chitosan) sources - that have been contrived into electrospun fibers. Furthermore, a relative study of these biomaterials for the fabrication of nanofibers by electrospinning and their characteristics viz. solution behavior, blending nature, as well as rheological and fiber attributes are discussed. The potential multidimensional applications of nanofibers (filtration, antimicrobial, biosensor, gas sensor, energy storage, catalytic, and tissue engineering) originating from these polysaccharides and their major impacts on the properties, functionalities, and uses of these electrospun fibers are compared and critically examined.

Water could be considered one of the essential natural resources on our planet. However, water contamination has become virtually ubiquitous during the past decades due to several factors, e.g., world population growth, water use in chemical production, and agriculture. Among contaminants, persistent organic pollutants (POPs) were widely spread during the last few decades and are now present all around the world. POPs are connected with several different illnesses, and therefore the removal of these pollutants from water is a challenge for coming years. Cyclodextrins (CDs) are environmentally friendly and cheap pollutant adsorbents due to their peculiar physicochemical properties. Moreover, CDs are relatively easy to use, and many techniques are reported for their functionalization. In addition, several CD derivatives are known and some of them are commercially available. CDs and CD-functionalized materials could be used for removal of different pollutants by using various methods, e.g., adsorption/extraction, soil washing, and electrokinetic/catalytic processes. This is the first review article that provides an overview of CDs/CD-based materials and their use in the remediation of POPs listed under the Stockholm Convention. The mechanisms of the POPs removal by CDs are also discussed.

A novel greener methodology is reported for the synthesis of titanium dioxide (TiO2) nanoparticles (NPs) using gum Arabic (Acacia senegal) and the characterization of the ensuing TiO2 NPs by various techniques such as X-ray diffraction (XRD), Fourier transform infrared, Raman spectroscopy, scanning electron microscopy–energy dispersive X-ray, transmission electron microscopy (TEM), high resolution-TEM, and UV–visible spectroscopy. The XRD analysis confirmed the formation of TiO2 NPs in the anatase phase with high crystal purity, while TEM confirmed the size to be 8.9 ± 1.5 nm with a spherical morphology. The electrode for the electrochemical detection of Pb2+ ions was modified by a carbon paste fabricated using the synthesized TiO2 NPs. Compared to the bare electrode, the fabricated electrode exhibited improved electro–catalytic activity toward the reduction of Pb2+ ions. The detection limit, quantification limit, and the sensitivity of the developed electrode were observed by using differential pulse voltammetry to be 506 ppb, 1.68 ppm, and 0.52 ± 0.01 μA μM–1, respectively. The constructed electrode was tested for the detection of lead content in plastic toys.

The inert nature of most commercial polymers and nanomaterials results in limitations of applications in various industrial fields. This can be solved by surface modifications to improve physicochemical and biological properties, such as adhesion, printability, wetting and biocompatibility. Polymer functionalization allows to graft specific moieties and conjugate molecules that improve material performances. In the last decades, several approaches have been designed in the industry and academia to graft functional groups on surfaces. Here, we review surface decoration of polymers and nanomaterials, with focus on major industrial applications in the medical field, textile industry, water treatment and food packaging. We discuss the advantages and challenges of polymer functionalization. More knowledge is needed on the biology behind cell–polymer interactions, nanosafety and manufacturing at the industrial scale.

Biosynthesis of nanomaterials is gaining attention as a sustainable, environmentally friendly, and reliable method for manufacturing a extensive array of nanostructures, such as metal/metal oxides ...

The use of polymers and nanomaterials has vastly grown for industrial and biomedical sectors during last years. Before any designation or selection of polymers and their nanocomposites, it is vital to recognize the targeted applications which require these platforms to be modified. Surface functionalization to introduce the desired type and quantity of reactive functional groups to target a cell or tissue in human body is a pivotal approach to improve the physicochemical and biological properties of these materials. Herein, advances in the functionalized polymer and nanomaterials surfaces are highlighted along with their applications in biomedical fields, e.g., antimicrobial therapy and drug delivery.

The disposal of natural wastes has become a global problem and the use of lower-grade gums is very limited owing to their impurities as well as sticky nature. Rather than disposing these wastes, nanoporous carbon (nC) has instead been synthesized by carbonization and exfoliation. The synthesized nC exhibits a substantially high surface area along with abundant micro/mesopores. This desirable and useful nature of nC is well-suited for water-driven effective electrical energy conversion, which enables the fast evaporation of water via a capillary action through nanopores. Under asymmetric wetting in a water container and ambient conditions, the nC-based energy harvesters showed high capability of electricity production and reliable output generation, easily turning on a blue light-emitting diode (2.5 V and 20 mA) using a stored power source. In summary, many energy harvesters can be manufactured for the scale-up of electricity, and the suitability of regenerated carbon nanomaterials for green energy harvesting can contribute toward alleviating chronic environmental issues.

To reduce the dependency on petro-based conventional plastics, research focusing on bioplastics derived from biological origin has gained precedence. Herein, we report an ecofriendly and a facile s...

The effect of the zeta potential of nano zero-valent iron (nZVI) and carbocatalyst on the activation of persulfate was investigated. The oxidation experiments were performed on three different compounds, with variously modified nZVI and three distinct carbocatalysts. From the obtained results, an evident linear correlation between nanoparticles’ zeta potential and reaction rate constants of these three compounds oxidation may be observed. This phenomenon is not mechanism-specific and occurs for the radical and non-radical processes. The present work indicates the critical influence of the surface charge of nZVI and carbocatalysts on the persulfate catalytic activation.

Lindane (γ-hexachlorocyclohexane) and its isomers (HCH) are some of the most common and most easily detected organochlorine pesticides in the environment. The widespread distribution of lindane is due to its use as an insecticide, accompanied by its persistence and bioaccumulation, whereas HCH were disposed of as waste in unmanaged landfills. Unfortunately, certain HCH (especially the most reactive ones: γ- and α-HCH) are harmful to the central nervous system and to reproductive and endocrine systems, therefore development of suitable remediation methods is needed to remove them from contaminated soil and water. This paper provides a short history of the use of lindane and a description of the properties of HCH, as well as their determination methods. The main focus of the paper, however, is a review of oxidative and reductive treatment methods. Although these methods of HCH remediation are popular, there are no review papers summarising their principles, history, advantages and disadvantages. Furthermore, recent advances in the chemical treatment of HCH are discussed and risks concerning these processes are given.

An economical and easy one-step method for the biosynthesis of highly stable molybdenum trioxide (MoO3) nanoparticles was developed using gum arabic as a bio-template; ensuing nanoparticles (NP) were characterized by X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, Raman spectroscopy, UV–visible spectroscopy, transmission electron microscopy (TEM) and energy-dispersive X-ray spectroscopy (EDX). The crystallinity and purity of MoO3 nanoparticles in the orthorhombic phase were confirmed by XRD analysis, and their rod-shaped identity (average sizes ranging from 7.5 to 42 nm) were observed by TEM. Cytotoxic effects of the NP were monitored using Hep G2 (human liver cancer) and HEK 293 (human embryonic kidney) cell lines via 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide assays. The results of this study revealed that MoO3 nanoparticles are nontoxic towards Hep G2 cell lines and displayed negligible toxicity, even at very high concentrations (1000 ppm), although had moderate toxicity towards HEK 293 cells. Furthermore, their catalytic activity was evaluated for the reduction of p-nitrophenol to p-aminophenol. Synopsis: Green synthesis of MoO3 nanorods using gum arabic demonstrated as an eco-friendly catalyst for the conversion of p-nitrophenol with negligible toxicity towards Hep G2 cell lines.

In the current paper, the production of homogeneous mixed nanocrystals based on Fe and Cu was successfully accomplished despite these two transition metals exhibiting extremely low miscibility in their phase diagram. The synthesis was carried out by the laser-mediated reduction of metal salts that were dissolved in different kinds of solvents, water, acetone and ethylene glycol. The greatest value of the methodology is that it allows the generation of mixed nanocrystals formed by transition metals with low miscibility in the presence of different solvents, taking metal salts as precursor agents, which are conventionally used in traditional wet synthesis techniques, but in contrast with the most popular approaches, the process requires neither special conditions nor hazardous reducing agents. Therefore, the presented methodology represents a clean and promising alternative for the synthesis of mixed nanocrystals composed of materials with low miscibility.

The food packaging industry explores economically viable, environmentally benign, and non-toxic packaging materials. Biopolymers, including chitosan (CH) and gelatin (GE), are considered a leading replacement for plastic packaging materials, with preferred packaging functionality and biodegradability. CH, GE, and different proportions of silver nanoparticles (AgNPs) are used to prepare novel packaging materials using a simple solution casting method. The functional and morphological characterization of the prepared films was carried out by using Fourier transform infrared spectroscopy (FTIR), UV–Visible spectroscopy, and scanning electron microscopy (SEM). The mechanical strength, solubility, water vapor transmission rate, swelling behavior, moisture retention capability, and biodegradability of composite films were evaluated. The addition of AgNPs to the polymer blend matrix improves the physicochemical and biological functioning of the matrix. Due to the cross-linking motion of AgNPs, it is found that the swelling degree, moisture retention capability, and water vapor transmission rate slightly decrease. The tensile strength of pure CH–GE films was 24.4 ± 0.03, and it increased to 25.8 ± 0.05 MPa upon the addition of 0.0075% of AgNPs. The real-time application of the films was tested by evaluating the shelf-life existence of carrot pieces covered with the composite films. The composite film containing AgNPs becomes effective in lowering bacterial contamination while comparing the plastic polyethylene films. In principle, the synthesized composite films possessed all the ideal characteristics of packaging material and were considered biodegradable and biocompatible food packaging material and an alternate option for petroleum-based plastics.

Polymeric nano-architectures are needed to address many of the critical challenges that we face today in areas such as energy, sustainability, clean water, health care, biotechnology, informatics, defence and security. Tree exudate gums are used in a multitude of applications, especially in the food industry but there are also numerous non-food applications such as biosynthesis and stabilization of metal/metal oxide nanoparticles, production of electrospun fibres, environmental bioremediation, biocatalysis, biosensors, and coordination complexes of metal–hydrogels, and for antimicrobial and biomedical applications. The present chapter reports an ecofriendly, facile synthetic route, biodegradable fibres, and nanoparticles prepared from the combination of tree gums with natural/synthetic materials. The major influencing factors such as biosynthesis protocol, conditions including pH, solvent, temperature, and their effect on physicochemical, structural, mechanical, thermal, and biodegradation of the composite fibres, and nanoparticles are briefly discussed. The developed tree gum-based biogenic nanoparticles, fibres, composites, and films are shown suitable for practical food packaging, energy harvesting, environmental, and biomedical applications.

Nanotechnology is increasingly being promoted to adopt “greener” technology that will improve the environmental performance of existing industries, reduce consumption of resources and energy, and enable the environmentally benign economic expansion. A novel approach in the field of sustainable/green nanotechnology is to develop advanced bio-composite materials with desirable properties using renewable and benign materials as exemplified herein by plant gum-based resources. The present chapter focuses on the fabrication and characterization of bioplastic fibers/films based on plant gums or other natural polymers via electrospinning or solution casting methods. Additionally, the integration of graphene oxide as a potential additive to blend in the plant gum based films/fibers to improve their physicochemical, tensile, thermal and antibacterial properties are investigated. Further, how the green technologies such as plasma, and γ-ray irradiation treatments on plant gum fibers/films have affected the enhancement of their structural, mechanical properties and biodegradability are also epitomized with suitable examples. The bioplastic fibers/films produced from bio-based materials played a noteworthy role in numerous imperative sectors, such as environmental bioremediation, medical, food carrying bags and packaging are appraised. This chapter would be of interest to the broad readership of material scientists, chemists, engineers and researchers associated with the sustainable developments and foresee the progress of economic and ecological products based on plant gums.

The assembly of bio-based macromolecules of gum kondagogu/sodium alginate (KO/SA) was fabricated using glycerol as a plasticiser and their optimum blending ratio was identified based on their physical and chemical, structural, mechanical, barrier, and morphological properties. The attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) analysis show that both biomacromolecules are well organised due to the hydrogen bond interaction between molecular chains involving the hydroxyl, carbonyl, and acetyl groups. Structural identification was performed by recording X-ray diffraction (XRD) spectra. Field emission scanning electron microscopy (FESEM) was used to identify the distinction between the surface of the films of biopolymers, and their conjugates, where the addition of SA increased the surface homogeneity and smoothness. The water contact angle of the blend films reached up to 81°, although the value for pure biomacromolecule films was very low. The blend films also exhibited high tensile strength (up to 24 MPa) compared to the pure biopolymer films. Investigation of film-forming ability, mechanical strength, permeability, transparency, and biodegradability of the developed KO/SA bio-macromolecular association may be established as green and sustainable food packaging films.

Rising concern about emerging and already persisting pollutants in water has urged the scientific community to develop novel remedial techniques. A new group of remediation methods is based on the modification of nanoscale zero-valent iron particles (nZVI), which are well known for treating volatile organic compounds and heavy metals. The properties of nZVI may be further enhanced by modifying their structure or surface using "green" polymers. Herein, nZVI was modified by a β-cyclodextrin polymer (β-CDP), which is considered an environmentally safe and inexpensive adsorbent of contaminants. This composite was used for the first time for the degradation of sulfamethoxazole (SMX). Coating by β-CDP not only enhanced the degradation of SMX (95%, under 10 min) by the nanoparticles in a wide pH range (3-9) and enabled their efficient reusability (for three cycles) but also made the coated nZVI less toxic to the model bioindicator microalga Raphidocelis subcapitata. Moreover, degradation products of SMX were found to be less toxic to Escherichia coli bacteria and R. subcapitata microalga, contrary to the SMX antibiotic itself, indicating a simple and eco-friendly cleaning process. This research aims to further stimulate and develop novel remedial techniques based on nZVI, and provides a potential application in the degradation of antibiotics in a wide pH range. Moreover, the wealth of available cyclodextrin materials used for surface modification may open a way to discover more efficient and attractive composites for environmental applications.

Environmental pollution causes irreversible damage to ecosystems and their structure. Therefore, the development of novel remedial techniques is a must for an effective response to emerging contaminants and those already persisting in the environment. The nanosized zero-valent iron (nZVI) is considered as an important nanostructure for the degradation of toxic compounds. Furthermore, the degradative potential of nZVI may be improved by surface modification. In this work nZVI was functionalized with β-cyclodextrin (β-CD), which is considered to be an environmentally-friendly and cheap adsorbent for toxic pollutants. Such a ‘green’ improvement not only enhances the activity of nZVI but also enables the conversion of 4-nitrophenol to 4-aminophenol, which under standard conditions is persistent and does not significantly react with bare nZVI. This research may help to find a solution to treat persistent organic pollutants (POPs) in aqueous environment.

Non-spherical metal-based and carbon-based nanostructures have found applications in every facet of scientific endeavors, including engineering and biomedical fields. These nanostructures attract attention because of their biocompatibility and negligible cytotoxicity. Chemical and physical methods have been used for synthesizing earlier generations of metal-based and carbon-based nanostructures with variable architectures, including nanorods, nanowires, nanodots and nanosheets. However, these synthesis strategies utilize organic passivators which are toxic to the environment and the human body. Biogenic synthesis of nanoparticles is becoming increasing popular because of the necessity to develop eco-friendly and non-toxic strategies. Nanoparticles synthesized by natural compounds have immense potential in the biomedical arena. The present review focuses on plant-mediated synthesis of metal-based and carbon-based non-spherical nanoarchitectures and the role of green synthesis in improving their activities for biomedical applications.

Electrospinning has garnered significant attention in view of its many advantages such as feasibility for various polymers, scalability required for mass production, and ease of processing. Extensive studies have been devoted to the use of electrospinning to fabricate various electrospun nanofibers derived from carbohydrate gum polymers in combination with synthetic polymers and/or additives of inorganic or organic materials with gums. In view of the versatility and the widespread choice of precursors that can be deployed for electrospinning, various gums from both, the plants and microbial-based gum carbohydrates are holistically and/or partially included in the electrospinning solution for the preparation of functional composite nanofibers. Moreover, our strategy encompasses a combination of natural gums with other polymers/inorganic or nanoparticles to ensue distinct properties. This early established milestone in functional carbohydrate gum polymer-based composite nanofibers may be deployed by specialized researchers in the field of nanoscience and technology, and especially for exploiting electrospinning of natural gums composites for diverse applications.

Wastewater from the textile industry has a substantial impact on water quality. Synthetic dyes used in the textile production process are often discharged into water bodies as residues. Highly colored wastewater causes various of problems for the aquatic environment such as: reducing light penetration, inhibiting photosynthesis and being toxic to certain organisms. Since most dyes are resistant to biodegradation and are not completely removed by conventional methods (adsorption, coagulation-flocculation, activated sludge, membrane filtration) they persist in the environment. Advanced oxidation processes (AOPs) based on hydrogen peroxide (H2O2) have been proven to decolorize only some of the dyes from wastewater by photocatalysis. In this article, we compared two very different photocatalytic systems (UV/peroxydisulfate and UV/H2O2). Photocatalyzed activation of peroxydisulfate (PDS) generated sulfate radicals (SO4&bull, &minus, ), which reacted with the selected anthraquinone dye of concern, Acid Blue 129 (AB129). Various conditions, such as pH and concentration of PDS were applied, in order to obtain an effective decolorization effect, which was significantly better than in the case of hydroxyl radicals. The kinetics of the reaction followed a pseudo-first order model. The main reaction pathway was also proposed based on quantum chemical analysis. Moreover, the toxicity of the solution after treatment was evaluated using Daphnia magna and Lemna minor, and was found to be significantly lower compared to the toxicity of the initial dye.

Heterogeneous catalysis is one of the fastest developing branches of chemistry. Moreover, it is strongly connected to popular environment-related applications. Owing to the very fast changes in this field, for example, numerous discoveries in nanoscience and nanotechnologies, it is believed that an update of the literature on heterogeneous catalysis could be beneficial. This review not only covers the new developments of heterogeneous catalysis in environmental sciences but also touches its historical aspects. A short introduction to the mechanism of heterogeneous catalysis with a small section on advances in this field has also been elaborated. In the first part, recent innovations in the field of catalytic air, water, wastewater and soil treatment are presented, whereas in the second part, innovations in the use of heterogeneous catalysis for obtaining sustainable energy and chemicals are discussed. Catalytic processes are ubiquitous in all branches of chemistry and there are still many unsolved issues concerning them.

A facile and eco-friendly approach is developed for the synthesis of a poly(3-hydroxybutyrate)–chitosan (PHB–chit) polymer conjugate, which is an ideal material for the synthesis of safer gold nanoparticles (nAu). The synthesized products are characterized by various electron-based, optical and spectroscopic techniques including the catalytic activity and the stability/toxicity of nAu. In contrast to the conventional synthesis approaches, the use of PHB–chit results in generation of a highly stable and size-controlled nAu material that exhibits important catalytic activity towards the reduction of 4-nitrophenol (4-NP) to 4-aminophenol, and at the same time shows no toxicity against living bacterial systems such as Escherichia coli or Staphylococcus aureus. The synthesis route reported herein would inspire future developments that circumvent toxicity issues of relevance to living systems while performing common catalytic experimentation.

In the current study, we explore the use of an eco-friendly laser-based methodology to fabricate Ag/TiO nanoparticles (NPs) with a highly controlled chemical composition, which serve to decorate the surface of Polyvinylidenefluoride (PVDF) nanofibrous membranes. Since these NPs can enhance the membranes’ oil–water separation performance and independently act as catalysts with the ability to purify water, we studied the samples’ separation capacity and, in parallel, the NPs pollutant degradation ability. Our findings evidence that membranes decoration by NPs with medium size (6.6 ± 2.2) nm, element composition 93.8 wt% Ti and 6.2 wt% Ag, where Ag locates in the surface, lead to a membranes’ loading of 1.31 ⋅ 1011 particles/cm2 or 0 . 13 μ g /cm2. Such superficial modification provides the membranes super-hydrophilicity resulting in improved oil–water separation performance through time and oil rejection percentage while the membrane’s fouling is negligible. Besides, the unique composition of these NPs brings a highly competitive catalytic activity ( κ c factor) of 2.82 L ⋅ g − 1 ⋅ s−1, implying that their multifunctional nature could expand the cleansing capabilities of nanofibrous membranes by separating water from oily polluted sources and separately catalyze the degradation of water dissolved organic pollutants. Thus, providing a groundwork for future developments in the truly cleansing of oily polluted water.

Peroxydisulfate (PDS) is a commonly used oxidant for in-situ chemical oxidation. There is still a lack of reliable methods for PDS determination, especially in the presence of other strong oxidants or other anions. Therefore, a new method was developed based on the evolution of a stable oxidation product from Acid Blue 40 (AB40) dye. The procedure was assessed in terms of its effectiveness for PDS determination in complex matrices, e.g., containing other oxidants. It was proven that the AB40 molecule selectively reacts with the sulfate radical, generated from PDS by heat activation, whereas it is inert towards other oxidants such as hydrogen peroxide, peroxymonosulfate ion or calcium peroxide. Mass spectrometry analysis, combined with theoretical investigations (density functional theory), confirmed the mechanism of this reaction and the product responsible for the color generation. The effect of AB40 concentration, activation temperature, presence of common anions, pH and other parameters were evaluated and a suitable analytical procedure for the PDS detection has been proposed. The limits of detection and quantification were determined to be 2 μM and 2.5 μM, respectively, which makes this method one of the most sensitive in the scientific literature for PDS determination. It is believed that this method may be very easily (colorimetry), quickly (30 min) and effectively used for groundwater and wastewater that possess complicated matrices.

Tree gums are a class of abundantly available carbohydrate polymers that have not been explored thoroughly in film fabrication for food packaging. Films obtained from pristine tree gums are often brittle, hygroscopic, and lack mechanical strength. This study focuses on the chemical modification of gum kondagogu using long-chain alkenyl groups of dodecenyl succinic anhydride (DDSA), an esterifying agent that introduces a 12-carbon hydrophobic chain to the kondagogu structure. The esterification reaction was confirmed by 1H nuclear magnetic resonance and Fourier-transform infrared spectroscopy. The effect of nano-cellulose as an additive on various film properties was investigated. The developed films were characterized for their mechanical, morphological, optical, barrier, antibacterial, and biodegradable properties. The inclusion of long-chain carbon groups acted as internal plasticizers and resulted in an amorphous structure with better film-forming ability, improved hydrophobicity, and higher elongation at break values. The modified films exhibited antibacterial properties and excellent biodegradability under aerobic conditions.

A facile green synthetic method is proposed for the synthesis of zinc oxide nanoparticles (ZnO NPs) using the bio-template Cinnamomum tamala (C. tamala) leaves extract. The morphological, functional, and structural characterization of synthesized ZnO NPs were studied by adopting different techniques such as energy dispersive X-ray analysis (EDX), high-resolution transmission electron microscopy (HR-TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-Visible spectroscopy, fourier transform infrared (FTIR) spectroscopy, raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The fabricated ZnO NPs exhibit an average size of 35 nm, with a hexagonal nanostructure. Further, the well-characterized ZnO NPs were employed for the photocatalytic degradation of methylene blue (MB) in an aqueous solution. The photocatalytic activity was analyzed by changing the various physicochemical factors such as reaction time, amount of photocatalyst, precursor concentration, and calcination temperature of the ZnO NPs. All the studies suggest that the ZnO synthesized through the green protocol exhibits excellent photocatalytic potency against the dye molecules.

Smart clothes can be described as textiles that change their behavior under some external factors (stimulants). The response of the smart cloth can be passive (just as a sensor) or active (where a combination of sensing and another reaction takes place). The materials involved in these textiles are crucial for many applications, especially for health related applications where the “wearables” can provide instantaneous monitoring and aid to people with certain disabilities. This work consists of two main parts: First it investigates the different materials used in smart clothing for monitoring the vital activities of the human body (e.g. the breathing rates) with an emphasis on piezoresistive structures as they work sensing elements for mechanical strains. Second this work presents the production of functional membrane samples based on synthesized pyrrolinone ester hydrazone dye with a preliminary investigation of their chemical and geometrical parameters, especially their sensitivity for monitoring the presence of ammonia to function as a smart textile based colorimetric chemosensor.

Recently electrospinning has gained significant attention due to unique possibilities to produce novel natural nanofibers and fabrics with controllable pore structure. The present study focuses on the fabrication of electrospun fibres based on gum karaya (GK), a natural tree gum, with polyvinyl alcohol (PVA), and functionalization of the membrane with TiO2 nanoparticles with further methane plasma treatment. The GK/PVA/TiO2 membrane was analyzed with several techniques including: fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX), and water contact angle, in order to characterize its morphological and physicochemical properties. The GK/PVA/TiO2 membrane was further successfully used for the degradation (under UV irradiation) of bisphenol A and diclofenac from aqueous solution. It was also observed that the degradation kinetics of these compounds are faster in comparison to the UV treatment alone.

The recent advances and potential applications of nanoparticles and nanofibres for energy, water, food, biotechnology, the environment, and medicine have immensely conversed. The present review describes a ‘green’ method for the synthesis and stabilization of nanoparticles and ‘green electrospinning’ both using tree gums (arabic, tragacanth, karaya and kondagogu). Furthermore, this review focuses on the impending applications of both gum stabilized nanoparticles and functionalized membranes in remediation of toxic metals, radioactive effluents, and the adsorptive removal of nanoparticulates from aqueous environments as well as from industrial effluents. Besides, the antibacterial properties of gum derivatives, gum stabilized nanoparticles, and functionalized electrospun nanofibrous membranes will also be highlighted. The functionalities of nanofibrous membranes that can be enhanced by various plasma treatments (oxygen and methane, respectively) will also be emphasized.

Gum polysaccharides are derived from renewable sources. They are readily available, inexpensive, non-hazardous and eco-friendly. Depending upon the source, gums may be categorized as microbial gums, plant exudate gums or seed gums. Naturally occurring gum carbohydrates find multiple applications in the biomedical arena, compared with synthetic compounds, because of their unique structures and functionalities. Gums and their biocomposites are preferred for sustained drug delivery because they are safe and edible as well as more susceptible to biodegradation. The present review provides a state-of-the-art conspectus on the industrial and biomedical applications of antimicrobial gum-based biocomposites. Different kinds of gums polysaccharides will first be addressed based on their sources. Metal-, carbon- and organic-based nanostructures that are used in gum nanocomposites will then be reviewed with respect to their industrial and biomedical applications, to provide a backdrop for future research.

This study investigates an environmentally benign approach to generate platinum nanoparticles (Pt NP) supported on the reduced graphene oxide (RGO) by non-edible gum waste of gum kondagogu (GK). The reaction adheres to the green chemistry approach by using an aqueous medium and a nontoxic natural reductant&mdash, GK&mdash, whose abundant hydroxyl groups facilitate in the reduction process of platinum salt and helps as well in the homogenous distribution of ensued Pt NP on RGO sheets. Scanning Electron Microscopy (SEM) confirmed the formation of kondagogu gum/reduced graphene oxide framed spherical platinum nanoparticles (RGO-Pt) with an average particle size of 3.3 &plusmn, 0.6 nm, as affirmed by Transmission Electron Microscopy (TEM). X-ray Diffraction (XRD) results indicated that the Pt NPs formed are crystalline with a face-centered cubic structure, while morphological analysis by XRD and Raman spectroscopy revealed a simultaneous reduction of GO and Pt. The hydrogenation of 4-nitrophenol could be accomplished in the superior catalytic performance of RGO-Pt. The current strategy emphasizes a simple, fast and environmentally benign technique to generate low-cost gum waste supported nanoparticles with a commendable catalytic activity that can be exploited in environmental applications.

Exudate gums are the natural secretions of different tree species and exhibit unique properties encompassing a wide variety of applications in food, pharmaceutical, adhesive, paper, textile, beverage, and other industries. The major exudates gums namely gum Arabic, gum Karaya, gum Tragacanth, gum Kondagogu, and gum Ghatti possess a unique range of functionalities. Biochemically, more than 90% of the gum biomass exists in the form of carbohydrate polymers (polysaccharides). Since these biopolymers are abundant, originate from renewable sources, and are relatively inexpensive and are nontoxic, they are amenable to both chemical and biochemical modifications. The present chapter focuses on “green” methods for the synthesis and stabilization of nanoparticles (NPs), and “green electrospinning” of tree gums to produce nanofibers and membranes. Furthermore, it considers the impending applications of gum fibers, NP-based gum functional materials, and gum electrospun fibers for environmental and biomedical applications.

The present study reports a green and sustainable method for the synthesis of titanium dioxide (TiO2) nanoparticles (NPs) from titanium oxysulfate solution using Kondagogu gum (Cochlospermum gossypium), a carbohydrate polymer, as the NPs formation agent. The synthesized TiO2 NPs were categorized by techniques such as X-Ray Diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy analysis, Raman spectroscopy, scanning electron microscope- Energy-dispersive X-ray spectroscopy (SEM-EDX), Transmission electron microscopy (TEM), High-resolution transmission electron microscopy (HR-TEM), UV-visible spectroscopy, Brunauer-Emmett-Teller (BET) surface area and particle size analysis. Additionally, the photocatalytic actions of TiO2 NPs were assessed with regard to their ability to degrade an organic dye (methylene blue) from aqueous solution in the presence of solar light. Various parameters affecting the photocatalytic activity of the TiO2 NPs were examined, including catalyst loading, reaction time, pH value and calcination temperature of the aforementioned particles. This green synthesis method involving TiO2 NPs explores the advantages of inexpensive and non-toxic precursors, the TiO2 NPs themselves exhibiting excellent photocatalytic activity against dye molecules.

Although the catalytic activation of persulfate by iron is now common in environmental sciences, there are still several obstacles, including the non-selectiveness and high cost of the production of the iron catalyst. Therefore, it is essential to develop fast and easy methods for producing an iron catalyst that exhibits high surface area properties and rapid catalytic activation of persulfate. In the present work, a chitosan-poly(3–hydroxybutyrate) conjugate (CS-PHB) was used to improve the synthesis of nanoscale zero-valent iron (nZVI). CS-PHB possesses among others two functional groups (carbonyl and amine) that are desirable for catalytic applications, including heterogeneous persulfate activation. The produced CS-PHB-nZVI particles showed an extensive surface area (113 m2/g) and, at the same time, superior activity in heterogeneous catalysis, which was tested and compared with others persulfate activation methods (heat, Fe2+, commercial nZVI). The most suitable activation conditions for complete degradation of 0.15 mM of the model pollutant (methyl orange; MO) were determined (i.e., a pH of 7, persulfate and CS-PHB-nZVI concentrations of 2 mM and 50 mg/L, respectively). The role of temperature in MO oxidation was evaluated by the Arrhenius equation, and the results showed that the estimated activation energy (Ea) was 27.1 kJ/mol. The MO degradation may be attributed to the generation of SO4 − in the system as a result of scavenging tests. A magnet can be used to easily separate the remaining catalyst. It is believed that due to it having several advantages over traditionally used nZVI, CS-PHB-nZVI may be successfully applied for catalytic remediation of contaminants that are reactive towards sulfate radicals.

A novel, lightweight (8 mg/cm3), conjugate sponge of karaya gum (Kg) and chitosan (Ch) has been synthesized with very high porosity (~98%) and chemical stability, as a pH-responsive adsorbent material for the removal of anionic and cationic dyes from aqueous solutions. Experimental results showed that Kg-Ch conjugate sponge has good adsorption capacity for anionic dye methyl orange (MO: 32.81 mg/g) and cationic dye methylene blue (MB: 32.62 mg/g). The optimized Kg:Ch composition grants access to the free and pH-dependent ionizable functional groups on the surface of the sponge for the adsorption of dyes. The studies on the adsorption process as a function of pH, adsorbate concentration, adsorbent dose, and contact time indicated that the adsorption capacity of MB was decreased with increasing pH from 5 to 10 and external mass transfer together with intra-particle diffusion. The adsorption isotherm of the anionic dye MO was found to correlate with the Langmuir model (R2 = 0.99) while the adsorption of the cationic MB onto the sponge was better described by the Freundlich model (R2 = 0.99). Kinetic regression results specified that the adsorption kinetics were well represented by the pseudo-second-order model. The H-bonding, as well as electrostatic interaction between the polymers and the adsorption interactions of dyes onto Kg-Ch sponge from aqueous solutions, were investigated using attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy, and the highly wrinkled porous morphology was visualized in depth by field-emission scanning electron microscopy (FE-SEM) analysis. Moreover, the samples could be reused without loss of contaminant removal capacity over six successive adsorption-desorption cycles. The hierarchical three-dimensional sponge-like structure of Kg has not been reported yet and this novel Kg-Ch sponge functions as a promising candidate for the uninterrupted application of organic pollutant removal from water.

Among various natural wastes, gum wastes pose major issues, as they are unusable and hard to be disposed due to their acidic and sticky nature. Herein, a rational synthetic strategy is employed to transform various kinds of gum wastes into micron-sized carbon, which also exhibit high tap density (1.4–1.7 g cm−3) desirable for practical application in lithium-ion batteries (LIBs). Gum karaya (GK) micron-size functional carbon (GKMFC) exhibits the most outstanding electrochemical performance, with a volumetric capacity of 175.4 mAh cm−3 at a current density of 3000 mA g−1 for 5000 cycles, and possesses ultra-stable high-rate cyclability (a capacity decay of only 0.001881% per cycle). Additional electrochemical analyses reveal that GKMFC exhibits stable structural integrity as well as minimal cell resistance even after cycling, showing its practical application as viable electrode for LIBs. This work sheds light on utilizing high tap density carbon from gum wastes for LIBs, which can also be applicable to other natural wastes and carbon.