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The idea of replacing liquid electrolytes with polymer electrolytes has been successful and the development of these electrolytes has provided acceptable results. With the start of using natural polymers in the polymer industry, as well as starch, these materials can be one of the most important candidates for the polymer matrix in electrolytes. In this study, starch has been investigated as a polymer electrolyte, poly[poly(ethylene glycol) methacrylate] (PEGMA) is grafted to the starch by radical polymerization, and synthesized copolymers are used as solid polymer electrolytes (SPEs). Furthermore, by adding N,N'-methylenebisacrylamide (MBA) as a cross-linking agent, gel polymer electrolytes (GPEs) are produced after swelling in the liquid electrolyte. After characterization, the synthesized polymer electrolytes are investigated in terms of electrochemical properties. The best ionic conductivity of 3.8 × 10-5 S cm-1 is obtained for SPEs whereas it is obtained 4.3 × 10-3 S cm-1 for GPEs at room temperature. The ion transfer number in the range of 0.47-0.91 confirms the compatibility between the electrolytes and electrode. Also, the prepared polymer electrolytes present excellent electrochemical properties, including, a wide electrochemical stability window above 4.7 V, good specific capacities in the range of 170-200 mAh g-1 with a storage capacity of more than 92 %, and Coulombic efficiency of about 98 % after 100 cycles at 0.2 C.
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Fontes de Energia Elétrica , Eletrólitos , Géis , Metacrilatos , Polietilenoglicóis , Amido , Eletrólitos/química , Amido/química , Polietilenoglicóis/química , Géis/química , Metacrilatos/química , Lítio/química , Íons/química , Condutividade Elétrica , Polímeros/químicaRESUMO
Self-indicating polymers have emerged as a promising class of smart materials that possess the unique ability to undergo detectable variations in their physical or chemical properties in response to various stimuli. This article presents an overview of the most important mechanisms through which these materials exhibit self-indication, including aggregation, phase transition, covalent and non-covalent bond cleavage, isomerization, charge transfer, and energy transfer. Aggregation is a prevalent mechanism observed in self-indicating polymers, where changes in the degree of molecular organization result in variations in optical or electrical properties. Phase transition-induced self-indication relies on the transformation between different phases, such as liquid-to-solid or crystalline-to-amorphous transitions, leading to observable changes in color or conductivity. Covalent bond cleavage-based self-indicating polymers undergo controlled degradation or fragmentation upon exposure to specific triggers, resulting in noticeable variations in their structural or mechanical properties. Isomerization is another crucial mechanism exploited in self-indicating polymers, where the reversible transformation between the different isomeric forms induces detectable changes in fluorescence or absorption spectra. Charge transfer-based self-indicating polymers rely on the modulation of electron or hole transfer within the polymer backbone, manifesting as changes in electrical conductivity or redox properties. Energy transfer is an essential mechanism utilized by certain self-indicating polymers, where energy transfer between chromophores or fluorophores leads to variations in the emission characteristics. Furthermore, this review article highlights the diverse range of applications for self-indicating polymers. These materials find particular use in sensing and monitoring applications, where their responsive nature enables them to act as sensors for specific analytes, environmental parameters, or mechanical stress. Self-indicating polymers have also been used in the development of smart materials, including stimuli-responsive coatings, drug delivery systems, food sensors, wearable devices, and molecular switches. The unique combination of tunable properties and responsiveness makes self-indicating polymers highly promising for future advancements in the fields of biotechnology, materials science, and electronics.
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Natural polymers as battery components have a number of advantages, including availability, biodegradability, unleakage, stable form, superior process, electrochemical stability, and low cost. In other sides, conductive polymers can improve the electrochemical properties of the battery, such as charge/discharge rates, cycling stability, and overall energy storage capacity. Therefore, the combination of these two materials can provide acceptable features. In this study, polymer electrolytes based on cellulose have been synthesized by solution casting method to prepare a thin polymer film. Then, polypyrrole (PPy) was blended with cellulose in different weight ratios. To prevent electrical conductivity of blends, PPy was used <10 wt%. The electrochemical properties of prepared electrolytes have been investigated by different methods. The results showed that ionic conductivity was increased by addition of PPy to cellulose due to the creation of pores and also due to the high dielectric constant of conductive polymers. All synthesized electrolytes had suitable ionic conductivity (in the range of 10-3 S cm-1), significant charge capacity, stable cyclic performance, excellent electrochemical stability (above 4.8 V), and high cation transfer number (between 0.38 and 0.66 for pure cellulose and the sample containing 10 wt% PPy).
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Celulose , Polímeros , Polímeros/química , Celulose/química , Lítio/química , Pirróis/química , Eletrólitos/química , ÍonsRESUMO
Brain cancers, especially glioblastoma multiforme, are associated with poor prognosis due to the limited efficacy of current therapies. Nanomedicine has emerged as a versatile technology to treat various diseases, including cancers, and has played an indispensable role in combatting the COVID-19 pandemic as evidenced by the role that lipid nanocarrier-based vaccines have played. The tunability of nanocarrier physicochemical properties -including size, shape, surface chemistry, and drug release kinetics- has resulted in the development of a wide range of nanocarriers for brain cancer treatment. These nanocarriers can improve the pharmacokinetics of drugs, increase blood-brain barrier transfer efficiency, and specifically target brain cancer cells. These unique features would potentially allow for more efficient treatment of brain cancer with fewer side effects and better therapeutic outcomes. This review provides an overview of brain cancers, current therapeutic options, and challenges to efficient brain cancer treatment. The latest advances in nanomedicine strategies are investigated with an emphasis on targeted and stimulus-responsive nanocarriers and their potential for clinical translation.
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Neoplasias Encefálicas , Portadores de Fármacos , Nanopartículas , Humanos , Neoplasias Encefálicas/tratamento farmacológico , Portadores de Fármacos/química , Nanopartículas/química , Nanopartículas/uso terapêutico , Nanomedicina/métodos , Barreira Hematoencefálica/metabolismo , COVID-19 , Animais , Sistemas de Liberação de Medicamentos/métodos , SARS-CoV-2 , Antineoplásicos/química , Antineoplásicos/uso terapêutico , Antineoplásicos/farmacologiaRESUMO
An environmentally friendly smart ink was developed by incorporating fluorescein into functionalized poly(methyl methacrylate) (PMMA) nanoparticles synthesized using an emulsifier-free emulsion copolymerization approach. The functional comonomers of 2-(dimethylamino)ethyl methacrylate (DMAEMA), acrylamide, hydroxyethyl methacrylate, and glycidyl methacrylate in 10 wt % with respect to methyl methacrylate were used to obtain the functionalized colloidal PMMA nanoparticles. Functional groups of the latex nanoparticles were characterized by Fourier-transform infrared spectroscopy. Field emission scanning electron microscopy results showed that all of the latex nanoparticles have nearly spherical morphologies with variations in size and surface smoothness due to the presence of different comonomers. Ultraviolet-visible and fluorescence spectra indicated that the fluorescein-doped latex nanoparticles containing the DMAEMA comonomer had the highest absorbance and fluorescence intensity. In the alkaline media, fluorescein turns to a dianion, showing a red shift and increased absorbance in the UV-vis spectroscopy. In addition, the electron inductive characteristics of the tertiary amine groups result in enhancing the conjugation of fluorescein molecules and increasing the fluorescence intensities. Therefore, the colloidal nanoparticles with amine functional groups were used in the formulation of a smart ink with applications in securing documents and fingerprints, encrypting banknotes and money, detecting latent fingerprints, crafting anticounterfeiting paper, and eventually providing optical detection and indication of surface scratches.
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A robust drug delivery system was created by grafting poly(dimethylaminoethyl methacrylate) (PDMAEMA) onto silica nanoparticles with two different lengths using an in situ atom transfer radical polymerization, resulting in the formation of a pH- and temperature-sensitive shell. The high molecular weight PDMAEMA demonstrated effective controlled drug release, and prevented drug release in healthy cells. Drug release occurred through polymer shell protonation at pH 5. The critical temperature of 41 °C facilitated rapid solvation of the shell polymers in the blood, preventing tissue accumulation and reducing toxicity compared to systems with lower critical solution temperatures. Field-emission scanning electron microscopy analysis and nitrogen adsorption/desorption analysis showed that the nanoparticles have a fine network, mesoporous structure, and a mean size of around 17 nm that show their excellent capacity for loading drugs. Fourier-transform infrared spectroscopy showed that all the modification steps and polymerization were successfully implemented. Thermogravimetric analysis showed PDMAEMA chains with two different lengths grafted onto the nanoparticles. Transmission electron microscopy analysis also showed grafted polymer chains on the hybrid nanoparticles. The release profile of model cancer drugs (doxorubicin and methotrexate) varied with pH and temperature, with high molecular weight PDMAEMA shells effectively preventing drug release at neutral pH. In vitro analysis using the HeLa cell line showed minimal toxicity in blank samples and significant release profile in acidic environment.
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Nanopartículas , Dióxido de Silício , Humanos , Temperatura , Células HeLa , Dióxido de Silício/química , Sistemas de Liberação de Medicamentos , Metacrilatos/química , Nanopartículas/química , Polímeros/química , Concentração de Íons de Hidrogênio , Portadores de Fármacos/químicaRESUMO
Imatinib mesylate, an anticancer drug, is prescribed to treat gastrointestinal stromal tumors and chronic myelogenous leukemia. A hybrid nanocomposite of N,S-doped carbon dots/carbon nanotube-poly(amidoamine) dendrimer (N,S-CDs/CNTD) was successfully synthesized and used as a significant modifier to design a new and highly selective electrochemical sensor for the determination of imatinib mesylate. A rigorous study with electrochemical techniques, such as cyclic voltammetry and differential pulse voltammetry, was performed to elucidate the electrocatalytic properties of the as-prepared nanocomposite and the preparation procedure of the modified glassy carbon electrode (GCE). A higher oxidation peak current was generated for the imatinib mesylate on a N,S-CDs/CNTD/GCE surface compared to the GCE and CNTD/GCE. The N,S-CDs/CNTD/GCE showed a linear relationship between the concentration and oxidation peak current of the imatinib mesylate in 0.01-100 µM, with a detection limit of 3 nM. Finally, the imatinib mesylate's quantification in blood-serum samples was successfully performed. The N,S-CDs/CNTD/GCE's reproducibility and stability were indeed excellent.
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Dendrímeros , Nanotubos de Carbono , Mesilato de Imatinib , Nanotubos de Carbono/química , Reprodutibilidade dos Testes , Limite de Detecção , Técnicas Eletroquímicas/métodos , EletrodosRESUMO
Colloidal materials have widely been used to develop innovative anticounterfeiting nanoinks for information encryption. Latex nanoparticles based on methyl methacrylate (MMA) and 2-hydroxyethyl methacrylate (HEMA) bearing hydroxyl functional groups were synthesized via semicontinuous miniemulsion polymerization. The size determination of the nanoparticles and microscopic results showed mostly spherical nanoparticles with a narrow size distribution and a mean size of about 80 nm. Two oxazolidine derivatives were physically doped at the surface of the nanoparticles to prepare photoluminescent polymer nanoparticles. Hydroxyl functional groups at the surface of the nanoparticles led to their hydrogen bonding interactions with the doped luminescent compounds. Optical analysis of the photoluminescent nanoparticles displayed different fluorescence emission and UV-vis absorbance intensities based on the amount of polar groups located at the surface of colloidal nanoparticles. Reducing the particle size to below 100 nm along with increasing the surface area can assist the decrease of the light reflectance and improvement of the latex nanoparticles' efficiency in the anticounterfeiting industry. This preparation methodology can efficiently provide remarkable photoreversible anticounterfeiting nanoinks used in different applications, such as print marking, security encoded tags, labeling, probing, and handwriting.
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Nanopartículas , Polímeros , Tamanho da Partícula , PolimerizaçãoRESUMO
Visual detection of analytes has been a significant challenge in the design and development of optical chemosensors. Sensing of analytes in aqueous solution by organic molecules has encountered some issues, such as poor water solubility and quenching of optical properties. In this study, a new category of smart dendritic macromolecules was designed and synthesized by functionalization of the poly(amidoamine) (PAMAM) dendrimer with spiropyran molecules to afford a photoluminescent dendritic structure (SP-PAMAM). Smart optical sensors were prepared by physical incorporation of four different oxazolidine derivatives containing hydroxyl and nitro substituted groups into the SP-PAMAM structure. Investigation of optical properties demonstrated photoinduced electron transfer (PET) between the spiropyran end group of SP-PAMAM and oxazolidine derivatives (in a concentration of about 0.0002 M), which can result in quenching of fluorescence emission of spiropyran photoswitch in the form of merocyanine (MC). Treatment of the oxazolidine-doped SP-PAMAM samples with metal ions resulted in changes in the PET mechanism (switching on or off), as observed in the case of Fe3+, Pb2+, Cu2+, Zn2+, Cd2+, Co2+, and Ni2+ by different oxazolidine derivatives through various mechanisms (increase or decrease of fluorescence emission). These smart photoluminescent dendritic macromolecules have potential applications for photodetection of metal ions in aqueous media as optical chemosensors. In addition, the smart macromolecules displayed disconnection of PET between MC and oxazolidine and also showed red fluorescence emission under acidic conditions (pH 1-5). It is due to the protonation of the MC to MCH form and demonstrates a remarkable red shift in fluorescence spectra. The pH-responsivity of smart macromolecules was used for designing a paper-based pH indicator for visual detection of spoilage in the food industry, especially in the case of milk. The prepared papers applied on cap of the milk bottles did not show any fluorescence emission in the case of fresh milk; however, a red fluorescence emission was observed after milk spoilage as a result of adsorption of acidic volatile components generated by bacterial degradation and oxidation process on the paper surface. The reported smart papers can serve as optical portable pH indicators for timely detection of spoilage in food materials, which are usable in food packaging as smart indicator tags.
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Elétrons , Nitrocompostos , Benzopiranos , Fluorescência , Indóis , Nitrocompostos/química , Água/químicaRESUMO
Cellulose and its derivatives are highly applicable in advanced applications on the basis of fluorescence phenomena. Carbon dots (CDs) have also appealing properties, such as high photoluminescence, easy synthesis pathway, cheap source materials, chemical stability, and easy functionalization. In this regard, combination of luminescent CDs with natural cellulosic materials could adjust or expand its desirable properties and have advanced applications. This review summarizes chemical and physical incorporation of CDs and graphene quantum dots into different types of cellulosic materials to yield smart fluorescent materials with applications in films, catalysts, bioimaging, drug delivery, anticounterfeiting, and fluorescence chemosensors for sensing pH, temperature, cations, anions, glucose, and aromatic amines. The challenges and future directions in fluorescent materials based on CDs are also briefly discussed. We hope that these studies will provide more consideration and curiosity for chemists, biologists, and materials scientists working in the field of fluorescent and CDs-containing cellulosic materials.
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Carbono , Pontos Quânticos , Carbono/química , Fluorescência , Corantes Fluorescentes/química , Luminescência , Pontos Quânticos/químicaRESUMO
Photochromic polymers, which are prepared by the incorporation of photochromic compounds into polymer matrices, show fluorescence emission along with color change under UV light irradiation. Polymer nanoparticles yield high chromic properties at low chromophore loadings, as they have a large surface area to absorb a high level of light irradiation. Particle size is a significant parameter to control optical properties, where the decrease of particle size results in a high light absorption and efficiency of photochromism and fluorescence emission. Reverse atom transfer radical polymerization was used to synthesize methyl methacrylate homopolymer and its copolymers with different comonomers to yield polymers with a narrow molecular weight distribution. Spiropyran was doped to the polymeric nanoparticles during nanoprecipitation to yield photochromic polymer nanoparticles. Particle size below 100 nm for the photochromic nanoparticles was shown by dynamic light scattering. Morphology investigation with microscopic analysis showed spherical morphology for nanoparticles. The photochromic properties of the polymer nanocarriers were studied in both acidic and alkaline media. The results indicated that the pH of the media as well as the copolymer composition significantly affect the optical properties. Therefore, the photochromic polymer nanoparticles could have potential applications as optical pH chemosensors by colorimetric and fluorometric detection mechanisms. The nanoparticles with hydroxyl- or amine-functional groups were shown to be highly efficient for pH chemosensor applications. Finally, photochromic cellulosic papers prepared from the photochromic polymer nanoparticles were highly applicable in the detection of acid vapors.
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Oxazolidine is a new category of stimuli-chromic organic compounds with unique characteristics in response to polarity, pH changes, water, light, and metal ions that were well-known as solvatochromism, acidochromism, hydrochromism, photochromism, and ionochromism, respectively. Therefore, oxazolidine derivatives have been developed for their potential applications in chemosensors, anticounterfeiting, and rewritable hydrochromic papers. In this study, various oxazolidine derivatives containing hydroxyl and naphthalene substituted groups were synthesized by using two different indolenine compounds. The synthesized oxazolidine derivatives were used for investigation of solvatochromism in different solvents, and also acidochromism in various pHs by using UV-Vis and fluorescence spectroscopies. In addition, the oxazolidine derivatives were coated on cellulosic papers using a layer-by-layer strategy to develop rewritable acidochromic papers for printing of security tags on cellulosic papers by using acidic and alkaline solutions as water-based inks. Therefore, the developed rewritable acidochromic papers could be used as security papers.
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Optical chemosensors and ionochromic cellulosic papers based on oxazolidine chromophores were developed for selective photosensing of metal ions and information encryption as security tags, respectively. The oxazolidine molecules have been displayed highly intense fluorescent emission and coloration characteristics that are usable in sensing and anticounterfeiting applications. Obtained results indicated that oxazolidine molecules can be used for selective detection of pb2+ (0.01 M), and photosensing of Fe3+, Co2+ and Ag+ metal ion solutions by colorimetric and fluorometric mechanisms with higher intensity and sensitivity. Also, oxazolidine derivatives were coated on cellulosic papers via layer-by-layer method to prepare ionochromic papers. Prepared ionochromic papers were used for printing and handwriting of optical security tags by using of metal ion solutions as a new class of anticounterfeiting inks with dual-mode fluorometric and colorimetric securities. The ionochromic cellulosic papers can be used for photodetection of metal ions in a fast and facile manner that presence of metal ions is detectable by naked eyes. Also, key-lock anticounterfeiting technology based on ionochromic papers and metal ion solution as ink is the most significant strategy for encryption of information to optical tags with higher security.
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Functionalization of carbon nanotube (CNT) with polymers has drawn much attention due to its wide range of applications. Polymer-functionalized CNT could exhibit variety of properties, such as responsivity to environmental stimuli, ability of complexation with metal ions, increased dispersibility in different solvents, higher compatibility with polymer matrix, etc. Chemical and physical methods have been developed for the preparation of polymer-functionalized CNT. Polymer chains are chemically bonded to the CNT edge or surface in the chemical methods, which results in highly stable CNT/polymer composites. "Grafting to", "grafting from", and "grafting through" methods are the most common chemical methods for polymer-functionalization of CNT. In "grafting to" method, pre-fabricated polymer chains are coupled with the either functionalized or non-functionalized CNT. In "grafting from" and "grafting through" methods, CNT is functionalized by polymers simultaneously synthesized by in situ polymerization methods. Conventional free radical polymerization (FRP) and also controlled radical polymerization (CRP) are the most promising methods for in situ tethering of polymer brushes onto the surface of CNT due to their control over the grafting density, thickness, and functionality of the polymer brushes. The main focus of this review is on the synthesis of polymer-functionalized CNT via both the "grafting from" and "grafting through" methods on the basis of FRP and CRP routs, which is commonly known as in situ polymerizations. Finally, the most important challenges and applications of the in situ polymer grafting methods are discussed, which could be interesting for the future works.
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HYPOTHESIS: Light-controlling of surface characteristics in polymeric coatings has been a significant research area because of its potential application in development of smart surfaces. Wettability of light-responsive polymeric coatings based on spiropyran photochromic compound could be tuned by light irradiation. This is mainly because of spiropyran isomerization between the hydrophobic and hydrophilic states. EXPERIMENTS: Light-responsive latex nanoparticles containing spiropyran moieties were synthesized by semi-continuous emulsion copolymerization of acrylate monomers, which have different chain flexibility depending on the copolymer composition. Photochromic properties of spiropyran in stimuli-responsive latex nanoparticles displayed dependence of photochromism intensity and its kinetics to flexibility of the polymer chains in addition to the polarity of media. Photoswitchable surface wettability of the spiropyran-containing acrylic copolymer coatings was investigated, where the photo-responsive coatings were prepared by solution casting and electrospinning methods. FINDINGS: The photoswitchable coatings prepared by solution casting and electrospinning methods showed significant differences in their physical characteristics and especially surface wettability. The polymeric coatings displayed water droplet contact angles in the range of 60-93°, which could reversibly be switched to 55-86° upon UV light (365 nm) illumination as a result of isomerization of the hydrophobic spiro form to the zwitterionic merocyanine form. The nanofibrous coatings prepared by electrospinning method displayed higher contact angles in the range of 120-136°, which was switched to 78-105° upon UV light irradiation. The developed photo-responsive coatings displayed highly-efficient photoswitching between the two hydrophobic and hydrophilic states as a response to UV and visible light irradiation. The photoswitchable nanofibrous coatings displayed ultrahydrophobic characteristics, where the colored water droplets were stable on their surface and could easily be adsorbed by a cellulosic tissue. In summary, the photoswitchable nanofibrous coatings could be applied for design and development of ultrahydrophobic materials with the ability of photo-controlling of surface wettability by light irradiation with tunable intensity.
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Counterfeiting and inverse engineering of security and confidential documents, such as banknotes, passports, national cards, certificates, and valuable products, has significantly been increased, which is a major challenge for governments, companies, and customers. From recent global reports published in 2017, the counterfeiting market was evaluated to be $107.26 billion in 2016 and forecasted to reach $206.57 billion by 2021 at a compound annual growth rate of 14.0%. Development of anticounterfeiting and authentication technologies with multilevel securities is a powerful solution to overcome this challenge. Stimuli-chromic (photochromic, hydrochromic, and thermochromic) and photoluminescent (fluorescent and phosphorescent) compounds are the most significant and applicable materials for development of complex anticounterfeiting inks with a high-security level and fast authentication. Highly efficient anticounterfeiting and authentication technologies have been developed to reach high security and efficiency. Applicable materials for anticounterfeiting applications are generally based on photochromic and photoluminescent compounds, for which hydrochromic and thermochromic materials have extensively been used in recent decades. A wide range of materials, such as organic and inorganic metal complexes, polymer nanoparticles, quantum dots, polymer dots, carbon dots, upconverting nanoparticles, and supramolecular structures, could display all of these phenomena depending on their physical and chemical characteristics. The polymeric anticounterfeiting inks have recently received significant attention because of their high stability for printing on confidential documents. In addition, the printing technologies including hand-writing, stamping, inkjet printing, screen printing, and anticounterfeiting labels are discussed for introduction of the most efficient methods for application of different anticounterfeiting inks. This review would help scientists to design and develop the most applicable encryption, authentication, and anticounterfeiting technologies with high security, fast detection, and potential applications in security marking and information encryption on various substrates.
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Counterfeiting of confidential documents has been a costly challenge for banks, companies, and customers. Encryption of invisible security marks, such as barcodes, quick response codes, and logos, in national or international confidential documents by high-security anticounterfeiting inks is the most significant solution for counterfeiting problems. Ecofriendly multi-color photoluminescent anticounterfeiting inks based on highly-fluorescent polymer nanoparticles functionalized with new oxazolidine derivatives were developed for the fast and facile encryption of security labels on cellulosic documents, such as paper currency, passport, and certificate. Depending on the polarity of functionalized polymer nanoparticles, a wide range of colors and fluorescence emissions were observed as a result of polar-polar interactions between the oxazolidine molecules and surface functional groups of the nanoparticles. The fluorescent polymer nanoparticles showed spherical, vesicular, and cauliflower-like morphologies resulted from different surface functional groups. Functional polymer nanoparticles displayed high stability and printability on cellulosic substrates due to hydrogen bonding interactions. The highly-fluorescent polymer nanoparticles were also used to prepare anticounterfeiting inks with different colors and fluorescence emissions. All the ecofriendly polymeric anticounterfeiting inks were loaded to stamps with specific marks, and then applied to different confidential documents. Printed labels displayed highly intense fluorescence emission in different colors (green, orange, pink, and purple depending on the matrix polarity) under UV irradiation (365 nm). These water-based multi-color fluorescent anticounterfeiting inks with highly intense, bright, and sensitive fluorescence emission have potential applications in encryption and authentication of security patterns.
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Photodetection of originality and authentication of security documents such as money, passport, bank note, and national card have been a significant challenge in recent decade. Using of advanced optical systems could remarkably reduce copy and counterfeiting of such national and international documents. Novel ecofriendly multi-color photoluminescent inks were developed for information encryption on cellulosic papers and optical authentication of confidential/original documents by synthesis of water-based latex nanoparticles modified with photoluminescent coumarin (blue emission) and two photochromic spiropyran derivatives (red and orange emissions). Some of the latexes with higher fluorescence emission were formulated to water-based inks, and then loaded to stamps with different marks for printing of quick response code, barcode, finger print, and other marks on cellulosic documents. All of the printed marks display ultra-bright blue, red, and orange fluorescence emissions upon UV irradiation, which have potential applications in encryption, security marking and optical authentication of confidential cellulose substrates.
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A series of hydrogel nanocomposites was fabricated by in situ polymerization of 2-(dimethylamino)ethyl methacrylate (DMAEMA) in presence of different amounts of (amine- and alkyl-modified) nanocrystalline cellulose (NCC). Modification and nanocomposites properties were proved by different analysis methods such as Fourier-transform infrared spectroscopy (FT-IR), dynamic light scattering (DLS), and field emission scanning electron microscopy (FE-SEM). The new hydrogel nanocomposites were applied for removing methyl orange (MO) used as anionic dye and presented in process water at different pH values. The effects of the fabrication process such as modification and content of NCC, contact time, and pH value on swelling ratio (SR), and equilibrium adsorption kinetics were studied. Results showed that the swelling ratio of PDMAEMA-based nanocomposites varied with the different types of nanoparticles showing the significant effect of the modification process. The MO adsorption into the hydrogel nanocomposites was affected by intermolecular and electrostatic interactions between functional groups of hydrogel and dye. The adsorption capacity decreased at high pH value, and it was significantly affected type of nanoparticles introduced into the hydrogel network. The addition of unmodified NCC did not affect adsorption kinetics significantly. Finally, adsorption kinetics was investigated by pseudo-first-order, pseudo-second-order and intraparticle diffusion models where pseudo-first-order model showed the best correlation with experimental results.
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Hidrogéis , Poluentes Químicos da Água , Adsorção , Compostos Azo , Celulose , Concentração de Íons de Hidrogênio , Cinética , Metacrilatos , Nylons , Espectroscopia de Infravermelho com Transformada de Fourier , ÁguaRESUMO
Cross-liked poly(2-hydroxyethyl methacrylate-co-methacrylic acid) seeds with different morphologies such as cauliflower-like, lobed spherical, and spherical were used in seeded emulsion polymerization (SEP) of 2-(dimethylamino)ethyl methacrylate (DMAEMA), 2-hydroxyethyl methacrylate (HEMA), and methacrylic acid (MAA). The morphological structure of produced composite particles was observed using field emission scanning electron microscopy (FE-SEM). The origin of the formation of different morphologies was discussed using various thermodynamic parameters such as solubility parameters and intermolecular forces between polymeric components involved. Also, the effect of the morphology of seed particles on the resultant structures was investigated. Results showed that morphology of fabricated composite particles is induced from morphology of seed particles with larger sizes. Finally, the fabricated composite particles were utilized in the controlled release of DOX. The effect of morphological changes of synthesized composite particles on the cumulative release behavior at acidic environment indicated the pH-sensitive nature of drug release through carriers. The particles with PDMAEMA shell showed the highest release of DOX at pHâ¯=â¯7.4 whereas PMAA shells displayed the least cumulative release. Inversely, the lowest cumulative release at pHâ¯=â¯1.2 was shown by PDMAEMA-coated carriers. Moreover, particles with spherical morphology had better drug release than cauliflower-like ones originated from smart nature of carriers.