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In this study, three PEG-maleated rosin polyesters were produced by reacting between maleated rosin and PEG with different molecular weights and served as surfactants. The surface characteristics of these PEG-maleated rosin polyesters were detected. The conformational transition and adsorption characteristics of these polyesters were analyzed with the reorientation theory on the water–air surface. The surfactant mole fraction at the water–air surface increased as surfactant concentration increased, while the solvent mole fraction was decreased. The amount of surfactant on the water–air surface at state 1 with a maximal molar area appeared one unimodal in distribution and that at state 2 occupying a minimal molar area appeared a sigmoid distribution with П growth. The calculated adsorption free energy from CMC value is lower than calculated micellization energy obtained from molecular area at state 2 indicates the polyethylene glycol-maleated rosin polyesters firstly spread on the water–air surface and then aggregated into micelles. The results lay a foundation for better understand the adsorption and self-assembly processes. The adsorption characteristics and conformational transition of three PEG-maleated rosin polyesters were investigated. Paper title: Adsorption Characteristics and Conformational Transition of Polyethylene Glycol-maleated Rosin Polyesters on the Water–Air Surface

Purpose This study aims to prepare low-cost biomaterials from renewable natural resources (rosin). Design/methodology/approach Preparation of different biomaterials, ethylene glycol maleic rosin (EGMR), glycerol maleic rosin, pentaerythritol maleic rosin and sorbitol maleic rosin (SMR) esters, then evaluated by stability studies, moisture absorption, swelling index parameters, thermogravimetric analysis and skin irritation studies. Findings The prepared rosin derivatives had excellent moisture safety, according to the results. From EGMR to SMR, the swelling indices increase. Research limitations/implications These rosin biomaterials were used in coating, especially in the field of pharmaceutical coating, and good results were obtained in this study. Practical implications As these biomaterials rosin derivatives have excellent moisture resistance, they are recommended for use as coating materials for moisture-sensitive drugs. Originality/value There has recently been a lot of interest in researching the effects of rosin derivatives in various drug delivery systems.

Rosin is renewable biomass with the potential to enhance wood properties. However, its high leaching rate restricts the durability of rosin impregnation. To immobilize rosin in wood structure, poly...

Pyrolysis behavior of resins is essential for their high-temperature application. Herein, the high-temperature stability and pyrolysis kinetics and mechanism of rosin glyceride (RGE), hydrogenated ...

Green renewable resource has become a global hot spot. In this study, naturally occurring resource rosin derivative (RAG) was used to prepared a cationic waterborne polyurethane (WPU) dispersion using n-methyl di-ethanolamine (MDEA) as an ion center and 1,3-bis(3-aminopropyl) tetramethydisiloxane (APTMDS) as a chain extender, and hexamethylene diisocyanate (HDI) as a hard segment. The effects of MDEA and APTMDS contents on the particle size and storage stability of the WPU dispersion was determined, in addition, thermo-mechanical and mechanical properties, and antibacterial property as well as water uptake of the resulting polyurethane films were thoroughly investigated. The results show that an increase in the APTMDS content considerably improved the mechanical properties, surface hydrophobicity and water resistance of the WPU films. Moreover, all WPU films exhibit enhanced antibacterial activity against Escherichia coli and Staphylococcus aureus with the increase in the MDEA and APTMDS contents.

The utilization of rosin to fabricate functional polymers has attracted great attention due to its unique structure and property. Herein, we prepared a new type of carboxyl-containing cross-linked rosin microspheres (CCRMs) using a renewable-resource rosin as the raw material through the suspension polymerization. For comparative purpose, vanillin methacrylate (VMA), styrene (St) and isobornyl methacrylate (IBOMA) were separately used to replace DAGMA as monomer for the preparation of microspheres. Our results indicated that the obtained porous CCRMs showed a broad size distribution ranging from mesopores (3–50 nm) to macropores (> 50 nm), whereas the counterparts derived from VMA, St or IBOMA showed a powder state. Moreover, the CCRMs exhibited moderately high thermal stability. The integration of DAGMA into polymer microspheres provided CCRMs with excellent adsorption ability, which exhibited robust selective cationic dye (e.g., methylene blue (MB) and crystal violet (CV)) adsorption from waste aqueous solution. The adsorption process was fitted well with the Langmuir isotherm and the pseudo-second-order kinetic model. The maximum adsorption capacity was observed to be 602.4 mg/g for CV at 40 °C, and 512.8 mg/g for MB at 20 °C. In general, the high dye adsorption properties suggest that CCRMs may be highly efficient in adsorption selectivity for some cationic dyes.

A series of tung oil-rosin-based polyester (TRP) used as internal sizing agents were prepared using rosin, tung oil, maleic anhydride, and glycerol. TRP structure and properties were examined using Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC) and gel permeation chromatography (GPC). The TRP latexes were subsequently used as internal sizing agents, and the sizing properties were evaluated using a scanning electron microscope (SEM), a video-based dynamic contact angle measuring device and a Cobb absorbency tester. The optimal conditions for preparing the TRP sizing agent were as follows: the hydroxy-carboxyl ratio of the material was 0.25; the maleic anhydride dosage was 20 % of rosin; and the tung oil dosage was 40 % of rosin. Under the best conditions, the sized paper Cobb-60 was 15.6 g / m 2 \text{g}/{\text{m}^{2}} , the tensile index was 45.1 N·m/g, the burst index was 3.1 kPa· m 2 {\text{m}^{2}} /g, and the tear index was 15.6 mN· m 2 {\text{m}^{2}} /g.

Natural chemicals obtained from the renewable resources were widely used in the modification of plant fibers. In this report, in order to develop thermoplasticity of materials, the bamboo powder (BP) after hydrothermal pretreatment (BP-LHW) was efficiently modified with natural rosin acid (BP-LHW-RA) by esterification reaction under heterogeneous condition. The results indicate that the modified BP-LHW-RA presents a strong peak at 1743 cm−1 in the FT-IR spectra, which attributed to the –C = O vibration of the ester group formed by the reaction between rosin acid and the BP-LHW, confirming that BP-LHW was successfully grafted with rosin acid. The C1/C3 ratio of BP-LHW-RA increased 1.35 times as compared with BP-LHW in XPS analysis. Meanwhile, the crystallization index of BP-LHW-RA decreased by 4.62%, and its surface became smooth and full. Moreover, the glass transition temperature of BP-LHW-RA was 200 °C. The work presents a green and feasible route to prepare bio-based materials with desired thermoplasticity by grafting natural rosin onto biomass substrate. The bio-based material with desired thermoplasticity was prepared by grafting natural rosin onto bamboo powder.

The effectiveness of Air entraining agent (AEA) in concrete under low air pressure in the plateau area decreased. A type of new AEA, named MRE was synthesized to increase bubbles` stability in fresh concrete under low air pressure. The performance of MRE solution and concrete with MRE were tested under 60 kPa and 100 kPa compared with commercially gemini AEA (DCC). The test results showed that the foam volume of MRE and DCC solution under 60 kPa was reduced by 3% and 9% than under 100 kPa. The bubble liquid film strength of MRE is 63% higher than that of DCC. For concrete with MRE and DCC under 60 kPa, the air content was 2% and 16% lower, the relative dynamic modulus of concrete reduced by 6% and 15%, and the bubble spacing factor under 60 kPa increased by 17% and 39% respectively compared with that under 100 kPa. MRE can increase the freeze-thaw resistance of concrete under low air pressure without affecting concrete strength and is suitable for high altitude concrete.

Solvent-based polychloroprene (CR) adhesive was formulated using four different types of tackifiers. Wood rosin (WD), coumarone-indene resin (CI), terpene-phenolic resin (TP) and para-tert-butyl ph...

It is known that the tremendous structural units in a polymer chain can result in a larger free volume of the bulk, which can effectively decrease the dielectric constant of the polymer. According to this design strategy, a novel rosin-based BCB monomer containing Si–O and characterized by a symmetrical molecular structure was successfully synthesized. Subsequently, an amorphous cross-linked network, with a dielectric constant of 2.44 and a dielectric loss of 2.02 × 10−3 at 1.0 MHz, was formed after the monomer was polymerized at an appropriate temperature. Additionally, the effects of the rosin skeleton on other properties of the modified BCB resin were studied. Compared with those of a BCB resin without a rosin skeleton, the dielectric properties, thermal stability, mechanical properties, and hydrophobicity of the rosin-modified BCB resin were significantly improved. The improvement of these properties is due to the presence of a hydrogenated phenanthrene ring in rosin, which is difficult to rotate and hinders the movement of the molecular chains in the modified BCB resin. Meanwhile, the rigidity and hydrophobicity of the hydrogenated phenanthrene ring can also improve the properties of the BCB resin. Thus, this study shows that the introduction of a rosin skeleton can significantly and comprehensively improve the properties of BCB materials.

Wood polymer composites (WPCs) were prepared via compression molding technique using wood flour and methacrylic anhydride modified epoxidized soybean oil (MAESO) copolymerized with triallyl maleopimarate (TMPA). Various percentages of TMPA were incorporated into the composite system to compare the properties of the final WPCs. TMPA was synthesized from rosin acid and the chemical structure was characterized by 1H-nuclear magnetic resonance (NMR) and Fourier transform infrared (FTIR) spectroscopy. The interaction between wood flour, MAESO and TMPA were revealed by FTIR and scanning electron microscope (SEM) study. Results demonstrated that TMPA was effective in enhancing the mechanical and thermal properties of the composites. Flame retardancy, biodegradability, chemical resistance, and dimensional stability significantly improved after the incorporation of TMPA into the composites. Wood polymer composites loaded with 30 wt% of TMPA exhibited maximum improvement in properties compared to other systems.

In the current context, the development of bio-based and high-performance materials is one of the main research priorities. This study aims to combine the outstanding properties of cellulose nanofibrils (CNFs) or nanocrystals (CNCs) with those of bio-based poly(lactic acid) (PLA). Three-phase multilayered materials (TMLs) were built up by complexing a dry CNF- or CNC-based film with two PLA sheets, using a heat-pressing process. Before the preparation of the nanocellulosic films, CNFs and CNCs were modified by the adsorption of a rosin-based nanoemulsion. The rosin mixture as a natural compound is of interest because of its low cost, renewability, hydrophobicity, and its antimicrobial and antioxidant properties. After demonstrating the efficiency of the complexing procedure, we investigated the barrier properties of the multilayered materials against both oxygen and water vapor, with highly encouraging results. In fact, the presence of nanocellulose as an inner layer between the two PLA films significantly enhanced the oxygen barrier, with a decrease in oxygen permeability comprised between 84 and 96% and between 44 and 50% for neat nanocelluloses and nanocelluloses with rosins as the inner layer, respectively. On the other hand, the antioxidant properties of the final multilayered materials including rosins were highlighted, with a highly encouraging radical scavenging activity close to 20%. Because of the simplicity and the efficiency of the proposed method, this study paves the way toward the development of hybrid multimaterials that could be highly attractive for food packaging applications.

A novel pH-responsive wormlike micellar viscoelastic solution was constructed by a rosin-based anionic surfactant (Na-MPA-AZO-Na) in the presence of cetyltrimethylammonium bromide (CTAB). The viscoelasticity, aggregate morphology, and pH-responsiveness of the pH-responsive wormlike micelles have been investigated through the method of rheology and cryogenic-transmission electron microscopy. Its corresponding mechanism has been studied using

Abietic acid is one of the main compositions of rosin and tall oil, it has a tricyclic molecular structure, which could be further modified into a branched saturated bicyclic substance with the process of hydro-creaking treatment. Branched decalin and its derivatives are main creaking products from abietic acid, which are promising aviation fuel components since they owe high density, good thermal stability, and low freezing point. In this work, two routes for the target aviation fuel production with abietic acid as raw material were investigated, and their reaction conditions were optimized. Under the optimal conditions, target aviation fuel with a yield of 45.8% saturated bicyclic products was obtained through the route of hydrogenation-cracking process. Meanwhile, a yield of 42.2% was obtained with the route of cracking-hydrogenation process. The branched saturated bicyclic compounds obtained from both processes had excellent fuel properties. Especially, the pour point of the fuel was below −75 °C, which makes the product could be potentially used as bio-aviation fuel in special areas, or as additive to improve low temperature performance of conventional bio-jet fuels. The investigation of this paper provided an efficient and green way for the bio-refinery of rosin or tall oil.

In situ forming matrix (ISM) is an injectable drug delivery system containing a drug-loaded polymeric solution. It was applied for local drug administration such as into a periodontal pocket for periodontitis treatment with an antimicrobial agent. ISM can transform with phase inversion into the solid-like matrix after contact an aqueous environment by solvent exchange mechanism. This study aims to develop ISM which various concentrations of rosin (R) as matrix former dissolved in organic biocompatible and biodegradable solvents such as N-methyl-2-pyrrolidone, dimethyl sulfoxide and 2-pyrrolidone. Physicochemical characterization and matrix formation behavior owing to phase inversion of R ISM were evaluated including pH, density, viscosity, contact angles, surface tension, expelling force through a syringe, matrix formation behavior and morphological change. The density of all R ISM exhibited in the range of 1.03-1.11 g/cm3 and contact angles (9.04-44.13°) indicated a good wetting property. Higher R concentration decreased pH of ISM owing to increased amount of abietic and pimaric acid from R while the viscosity, contact angles and force for expelling a syringe were increased. The viscosity of R ISM in dimethyl sulfoxide was less than that in 2-pyrrolidone; thus, ISM using dimethyl sulfoxide as a solvent exhibited good injectability. ISM comprising R concentration > 30%w/w promoted a faster matrix growth in which the amount of occurred R matrix was enhanced with time and the rate of matrix formation was lower with time. Doxycycline Hyclate (Dx)-loaded 40%w/w ISM in dimethyl sulfoxide (Dx-DR) had pH of 3.70, density of 1.1084 ± 0.0005 g/ml, viscosity of 35.72 ± 0.00 cPs, contact angles of 26.87 ± 2.40°, surface tension of 37.11 ± 0.11 mN/m and expelling force of 23.98 ± 0.18 N. It showed the sustainable Dx release in simulated crevicular fluid and the efficient antimicrobial activity against Staphylococcus aureus and Porphyromonas gingivalis. Thus, this phase inversion induced R ISM using dimethyl sulfoxide as a solvent showed potential as an antimicrobial agent-loaded drug delivery system for periodontitis treatment.

The search for renewable fuels or components which may improve or replace fossil fuels is an important step towards a sustainable future. In particular, the pine oleoresin produced by conifer trees, which is composed by turpentine oil and non-volatile rosin, may be transformed into alternative fuels. In this work, combustion of six molecules which can be obtained from oleoresin either by distillation (i.e., α- and β-pinene) or by further oxyfunctionalization (nopol, terpineol, myrtenol, and borneol) was studied to assess the potential of pine oleoresin as raw material for biofuels. Emission indices of the main pollutants (carbon monoxide-CO, unburned hydrocarbons-UHC, and nitrogen oxides-NOx) were obtained in non-premixed co-flow laminar flames of the oleoresin-derived molecules blended with n-heptane. The main characteristics of the flames (i.e., temperature and height) were also determined. Significant increase in flame temperature and reduction in CO and UHC emissions with respect to n-heptane were observed with nopol, terpineol, and myrtenol, along an increase in NOx emissions, suggesting an improvement in combustion performance. In addition, differences in emission indices, evidenced for these molecules (even between α- and β-pinene), suggest the importance of the molecular structure in the combustion reaction.

Conversion of rosin to its pentaerythritol ester provides a means of improving its water resistance, alkali resistance, and oxidation resistance, thereby increasing its stability. Rosin pentaerythritol ester is much more amenable to industrial applications than the parent compound. To overcome the difficulty of catalyst recovery and its associated high cost during the synthesis of rosin pentaerythritol ester, Fe3O4-supported ZnO catalysts, such as Fe3O4@ZnO and Fe3O4@SiO2–ZnO, have been designed and synthesized. The structures, morphologies, and compositions of the materials have been characterized by TEM, XRD, and XPS. The results of esterification reactions demonstrate that Fe3O4@SiO2–ZnO has excellent catalytic performance and stability. The degree of esterification in the production of rosin pentaerythritol ester reached 87.9%, far exceeding the yields attained with other catalysts. Moreover, the catalyst could be reused five times without incurring a loss of activity. The effects of zinc source, zinc loading, and reaction conditions on the esterification have been investigated in detail. This study provides a class of heterogeneous catalysts with excellent properties for the synthesis of rosin pentaerythritol ester. In our paper, the optimum process conditions for obtaining rosin pentaerythritol ester have been identified as zinc nitrate as the zinc source, a theoretical loading of zinc source of 0.45 g, a reaction temperature of 250 °C, a reaction time of 5 h, and a catalyst loading of 0.2 g, when starting from rosin (15 g) and pentaerythritol (1.7 g). The conversion rate was 87.9%, and the acid value was 25.0 mg KOH g−1. This research provides an improved protocol for the rosin esterification reaction.

Present work focused on synthesis of green hydrogel polymer of gum rosin alcohol/psyllium crosslinked poly (acrylic acid) [(GrA-Psy)-cl-PAA] under vacuum condition. Use of both psyllium and gum rosin alcohols as backbones could lessen the burden on the environment, as more natural aspect is drawn in the hydrogel polymer. The various reaction parameters for the synthesis of hydrogel polymer were systematically optimized as a function of percentage swelling. The optimized ecofriendly hydrogel polymer was characterized using XRD, FTIR, FE-SEM and TGA techniques, which supported the successful formation of crosslinked three-dimensional network structures. (GrA-Psy)-cl-PAA was further studied as an adsorbent for the removal of methylene blue dye from an aqueous solution. Adsorption parameters such as the amount of adsorbent and pH were optimized to obtain the maximum percentage of dye removal. Kinetics of the adsorption process was analyzed using pseudo-first-order, pseudo-second-order and Elovich kinetic models. Adsorption kinetics followed pseudo-second-order model (non-linear) for all the concentrations studied. Non-linear forms of Langmuir, Freundlich and Dubinin-Kaganer-Radushkevich isotherm models were studied for the adsorption process and it was observed that it goes well with both Langmuir and Freundlich isotherms. Thermodynamic parameters were also evaluated which indicated that the adsorption process was exothermic and spontaneous. Furthermore, the candidate polymer retained a reusability tendency for two consecutive cycles of adsorption/desorption. Thus, the synthesized novel material was taken as a potential to act as green adsorbent in treatment of industrial wastewater.

A nonionic surfactant based on chitosan and rosin, i.e. dehydroabietyl glycidyl ether grafted hydroxypropyl chitosan (DAGE-g-HPCS), was synthesized for the first time through reaction between hydroxypropyl chitosan (HPCS) and dehydroabietyl glycidyl ether (DAGE). The surface activities of DAGE-g-HPCS in aqueous solution were investigated via determination of surface tension, and its emulsifying ability was evaluated according to the stability time of emulsion composed of benzene-water with DAGE-g-HPCS as emulsifier; the foam stability was evaluated using the oscillation method. Through modulating the molecular weight of HPCS and the grafting degree (DG) of DAGE-g-HPCS, the emulsion stability and foam stability were surprisingly controllable. Compared to HPCS and specific emulsifier, the stability time of emulsion composed of benzene-water with DAGE-g-HPCS showed a remarkable performance with DG of 16.5% as the emulsifier was 7320 s, and the foam retention of DAGE-g-HPCS with 2.0 g·L-1 was 91.5%. Simultaneously, the critical micelle concentration (CMC) of DAGE-g-HPCS decreased with increased DG, while the emulsifying ability and foam stability exhibited opposite trend. The CMC, emulsifying ability, and foam stability of DAGE-g-HPCS increased with decreased HPCS molecular weight. These results demonstrated that the DAGE-g-HPCS was an excellent surfactant that should be considered as a promising substitute for petrochemical nonionic surfactant.

Rosin and cellulose nanocrystals (CNCs) are easily extracted from agricultural pines/conifers and natural cellulose, and poly(3-hydroxybutyrate- co-3-hydroxyvalerate) (PHBV) are extracted from agri...

As the important part of liquid packaging board, the middle layer is generally produced from a mixed pulp furnish by unbleached softwood kraft pulp and high-yield pulp (HYP). However, the addition of HYP would bring unsatisfactory properties (e.g. hydrophilicity) to liquid packaging board. Herein, in this study, the sizing performance of middle layer of liquid packaging board was evaluated by varying the kraft pulp to HYP ratios of middle layer, the dosage of sizing agent and cationic additives etc. It showed that the edge penetration value and Cobb value of middle layer illustrated a better liquid repellence with the addition of sizing agent. The improved sizing performance of the middle layer of liquid packaging board can be ascribed to the excellent performance of the added cationic additive (polyethyleneimine (PEI), alums) for trapping anionic trash via neutralization/flocculation effects. In addition, a binary cationic additive system (Al2(SO4)3-PEI) was proposed to study the improvement on the sizing performance. It was found that a desirable liquid repellence ability can be successfully achieved at a binary additive system containing 1.5% of Al2(SO4)3 and 0.2% of PEI, even when dosage of rosin sizing agent was reduced to 0.5%. The study put forwards a practical approach to improve the sizing performance, especially the liquid repellence ability of liquid packaging board when containing HYP.

The aim of this study is to estimate antifouling and anticorrosion potential of organic extracts from Pseudoalteromonas piscicida 2202. Field tests of rosin-based experimental paint indicate that butanol extract of P. piscicida 2202 effectively prevents biofouling for 3 months. A protective film forms at the metal/solution interface in the presence of butanol extract, which leads to a decrease in the mild steel corrosion rate. The EIS method has shown that the incorporation of butanol extract in rosin-based paints improves the barrier properties of the coating by reducing the water uptake.

The aim of this work was to investigate a possibility of preparing composite zein/natural resin (shellac and rosin) nanoparticles by antisolvent co–precipitation from their aqueous ethanol solutions. Influence of zein/resin mass ratio (1/0, 0.8/0.2, 0.5/0.5, 0.4/0.6 and 0/1) and pH (2–12) on particle size, d, and zeta potential, , of the prepared particles was studied. The functional properties of zein/rosin composite nanoparticles were evaluated by studying carvacrol encapsulation. It was shown that the antisolvent precipitation can be successfully used to prepare the shellac and rosin nanoparticles, as well as the composite zein/shellac and the zein/rosin nanoparticles. Colloidal properties, d and , of the obtained nanoparticles are influenced by the zein/ /resin mass ratio and the pH of nanoparticles’ dispersions. The isoelectric point of composite nanoparticles can be modulated by varying the zein/resin mass ratio. It was found that the zein/rosin nanoparticles are suitable for carvacrol encapsulation, where carvacrol release is enhanced by increasing the rosin share in the composite zein/rosin nanoparticles. [Project of the Serbian Ministry of Education, Science and Technological Development, Grant no. III 46010/3]

[EN] The present study aims to investigate the effects of gum rosin (GR) microspheres coating over the hydrophobicity of the outer layer of a polypropylene (PP) based surgical face mask. The gum rosin coating was deposited over the surface of the face mask outer layer by electrospraying technique. The deposition of GR microspheres was confirmed by field emission scanning electron microscopy (FESEM) and Fourier transform infrared spectroscopy (FTIR) analysis. The thermal analysis determined a cooperative effect between the microspheres and the mask fibre to increase the maximum degradation rate temperature and the onset degradation temperature. To follow the effect of the GR microspheres coating over the hydrophobicity of the surgical face mask, FESEM and wettability analyses were conducted before and after 3, 6, and 9 h of wearing time. In the FESEM image, it was seen that the microsphere was homogeneously distributed over the nonwoven fibre and its presence increases the roughness of the fibres due to the bulge of microspheres. The wettability measurements suggest that the microspheres coating helps to keep the original hydrophobicity of the outer layer of the surgical face mask even after 6 h of wearing time. Indeed, after 9 h of wearing time, the water contact angle (WCA) of the GR coated face mask is higher than the WCA of the surgical face mask without the coating at 3 h of wearing time. Therefore, the gun rosin microspheres coating improved the hydrophobicity of the surgical face mask which may allow improved protection and/or extended lifetime of use., This research was funded by the Spanish Ministry of Economy and Competitiveness (MINECO), project: PROMADEPCOL (MAT2017-84909-C2-2-R). Cristina Pavon thanks Santiago Grisolía fellowship (GRISOLIAP/2019/113) from Generalitat Valenciana. Miguel Aldas thanks Secretaria de Educación Superior, Ciencia, Tecnología e Innovación (SENESCYT, Ecuador) and Escuela Politécnica Nacional.

The morphology and physicochemical properties of ordered molecular aggregates are closely related to surfactant molecules. Herein, a rosin-based amine oxide surfactant containing a large hydrophobic group (abbreviated R-10-AO) was synthesized from dehydroabietic acid, which is an important derivative of rosin. Cryogenic transmission electron microscopy (cryo-TEM) images and small-angle X-ray scattering (SAXS) showed that at a concentration of ∼5 mM, R-10-AO molecules formed flexible nanobelts with a thickness of only 2–3 nm. The width of these nanobelts was 50–150 nm and the length was more than 1 μm. The formation of the stable nanobelts arose from the strong van der Waals forces of the bulky hydrophobic portions of R-10-AO in solution, facilitating the stability of the asymmetrical aggregates. Rheological tests showed that the formed nanobelts were thermodynamically stable. The entanglement of these nanobelts led to significant viscoelasticity of the solutions. The zero-shear viscosity (η0) of the R-10-AO solution reached 10 Pa s at a concentration of 5 mM, which is much greater than that of most wormlike micellar solutions. This work provides the inspirations of preparing aggregates with novel properties using natural products.

Rosin is an abundantly available natural product. In this paper, for the first time, a rosin derivative is employed as the main monomer for preparation of epoxy vitrimers to improve the mechanical properties of vitrimers. Novel epoxy vitrimer networks with dynamic reversible covalent boronic ester bonds are constructed by a reaction between thiols in 2,2′–(1,4–phenylene)–bis (4–mercaptan–1,3,2–dioxaborolane) (BDB) as a curing agent and epoxy groups in the rosin derivative. The rosin-based epoxy vitrimer networks are fully characterized by Fourier transform infrared spectroscopy (FTIR), an equilibrium swelling experiment, and dynamic mechanical analysis (DMA). The obtained rosin-based epoxy vitrimers possess superior thermostability and good mechanical properties. Due to transesterification of boronic ester bonds, rosin epoxy vitrimer network topologies can be altered, giving welding, recycle, self-healing, and shape memory abilities to the fabricated polymer. Besides, the effects of treating time and temperature on welding capability is investigated, and it is found that the welding efficiency of the 20% C-FPAE sample is &gt, 93% after treatment for 12 h at 160 °C. Moreover, through a hot press, the pulverized samples of 20% C-FPAE can be reshaped several times and most mechanical properties are restored after reprocessing at 200 °C for 60 min. Finally, chemical degradation is researched for the rosin-based epoxy vitrimers.

Rosin is an abundant natural product. In this paper, for the first time, a rosin derivative is employed as a monomer for the preparation of polyurethane vitrimers with improved properties. A novel rosin-based polyurethane vitrimers network was constructed by the reaction between isocyanates (HDI) as curing agent and monomers with alcohol groups modified from rosin. The dynamic rosin-based polyurethane vitrimers were characterized by FTIR and dynamic mechanical analysis. The obtained rosin-based polyurethane vitrimers possessed superior mechanical properties. Due to the dynamic urethane linkages, the network topologies of rosin-based polyurethane vitrimers could be altered, contributing self-healing and reprocessing abilities. Besides, we investigated the effects of healing time and temperature on the self-healing performance. Moreover, through a hot press, pulverized samples of 70%VPUOH could be reshaped several times, and the mechanical properties of the recycled samples were restored, with tensile strength being even higher than the of that of the original samples.

Supramolecular hydrogels have attracted great attention due to their special properties. In this research, bio-based supramolecular hydrogels were conveniently constructed by heating and ultrasounding two components of dehydroabietic acid with a rigid tricyclic hydrophenanthrene skeleton and morpholine. The microstructures and properties of hydrogels were investigated by DSC, rheology, SAXS, CD spectroscopy, and cryo-TEM, respectively. The critical gel concentration (CGC) of the hydrogel was 0.3 mol·L−1 and the gel temperature was 115 °C. In addition, the hydrogel showed good stability and mechanical properties according to rheology results. Cryo-TEM images reveal that the microstructure of hydrogel is fibrous meshes, its corresponding mechanism has been studied using FT-IR spectra. Additionally, oil-in-water gel emulsions were prepared by the hydrogel at a concentration above its CGC, and the oil mass fraction of the oil-in-water gel emulsions could be freely adjusted between 5% and 70%. This work provides a convenient way to prepare bio-based supramolecular hydrogels and provides a new method for the application of rosin.

The poor mechanical properties and disadvantages of catalysts limit the application of self-healing materials. To address these issues, catalyst-free self-healing bio-based polymers (AESO-EMPA polymers) with robust mechanical properties were prepared using epoxidized maleopimaric anhydride (EMPA) and aminated epoxidized soybean oil (AESO). The AESO-EMPA polymers are recyclable and exhibit self-healing and shape memory because of the dual-dynamic network of multiple H-bonds and dynamic ester bonds in the structure. Under the synergistic catalysis of the tertiary amines and hydroxyl groups originated from the polymers, the polymers in this study achieve network rearrangement without the need for additional catalysts. The polymers also exhibit excellent mechanical properties with a tensile strength of 29.1 ± 0.25 MPa and a Tg of 80.2 °C owing to the unique rigid backbone of rosin and the dual-dynamic network. The AESO-EMPA polymers can be used as reusable adhesives and exhibit excellent shear strength and repair rates.

Preparation and application of sustainable polymers derived from renewable resources are of great significance. The aim of this study is to synthesize a kind of sustainable polymeric micelles from rosin and vegetable oils via atom transfer radical polymerization (ATRP) and to investigate the doxorubicin delivery properties of these micelles. Dehydroabietic acid–based poly lauryl methacrylate (DA-PLMA) with narrow PDI of 1.13 was prepared in a well-controlled process using rosin as an ATRP initiator. Thereafter, carboxylic groups were introduced to form poly methacrylic acid (PMAA) moieties in DA-PLMA polymer via acid hydrolysis. The resulted DA-PLMA-PMAA could self-assemble in water to form pH-dependent polymeric micelles with a diameter of ∼65 nm and PDI as low as 0.105. Owing to the existence of rosin, DA-PLMA-PMAA micelles also showed self-fluorescence properties. In addition, Dox-loaded micelles were prepared in aqueous solution with the drug-loading capacity as high as 16.0% and showed sustained-release characteristics. These results demonstrate great promise for designing polymeric micellar from rosin and vegetable oils.

A kind of polymerizable dispersant based on natural rosin was used to disperse single-walled carbon nanotubes (SWNTs) in aqueous solution followed by in situ free-radical polymerization to achieve a controllable SWNTs dispersion, that not only can be controlled by CO2/N2, but can also be recycled and redispersed in CO2-saturated water after drying without sonication.

A feasible method has been developed for the morphology control of ordered supermicroporous silicas by adopting a kind of rosin-based surfactant as the templating agent. By adjusting the molar ratio of sodium silicate (SS) and ethyl acetate (EA), the morphologies of the materials can be changed from hollow sphere to hollow tube, and solid rod, while the degree of ordering of the samples showed a trend of firstly increasing and then decreasing. When the molar ratio of SS/EA was 0.38, an ordered supermicroporous silica with a hollow tubular morphology was obtained. The material had a surface area of 645.5 m2/g, a pore volume of 0.3 cm3/g, and a pore size distribution centered at 1.8 nm. When the molar ratio of SS/EA was increased to 0.46, the resulting sample exhibited a solid-rod morphology with a highly ordered hexagonal supermicroporous structure. This material had a large surface area of 1478.1 m2/g, a high pore volume of 0.7 cm3/g, and a uniform pore size distribution centered at 2.0 nm.

The paper shows that creation of materials with antibacterial and antifungal action presupposes an introduction of additives in them. One of the directions concerning fight against mold fungi is an inclusion of biocide additives having vegetable origin in structure of polymer materials used for manufacturing packing products. The main mission of anti-microbial additives is reduction of microbe amount in product mass and on its surface. Activity of anti-microbial compounds depends on the following parameters: concentration of active component, pH, temperature, polymer type, introduction method (with plasticizer or in melting state) and time period of their contact with polymer. In addition it is necessary to take into account such not unimportant factor as sensitivity of micro-organisms. Modern film polymer materials ensure only a certain level of product protection. They can not targetedly affect biochemical and microbiological changes in a packing product. It is necessary to develop new packing materials with selective permeability that create a barrier on the way of extremely intensive gas and moisture exchange, outside microflora flow, and prevent an evolution of undesired micro-organisms on packing products. Polymers have been selected as a basis for a bactericide packing material. Investigations have shown that composition including PEHP 98% (polyethylene of high pressure) + DGR (disproportionate gum rosin) + DETA (diethylenetriamine) has inhibited (hindered) sufficiently in a good way growth of mold fungi and PEHP composition with additives of tallow pitch and polyethylenepolyamine has demonstrated a rapid deterioration of strength characteristics and an increase in additive of the supposed mixture including pine oleoresin (POR) with DETA and DGR (with DETA more than 2%) hinders rapidly strength material characteristics.

Abietic acid is an abundant renewable natural resource. Pentaerythritol rosin ester (PRE), which is synthesized by esterification of abietic acid and pentaerythritol, is notably environmentally friendly. In our study, we first report PRE as an environmentally friendly multifunctional additive in vegetable oil-based lubricant. The dynamic viscosity, kinematic viscosity, thermal stability and oxidation stability were investigated. The dynamic viscosity of rapeseed oil (RO) and soybean oil (SO) increased by 136.11% and 179.3% at 25 °C when 20 wt% of PRE was added. The viscosity results indicated that PRE can significantly increase the viscosity of RO and SO base oils to expand their range of applications. Moreover, lubricant samples with PRE had higher thermal stability and oxidation stability compared with pure RO and SO. The onset temperature (OT) of oxidation of RO and SO increased by 7.7 °C and 12.6 °C, respectively, when the concentration of PRE was 20 wt%. The oxidation induction time (OIT) of RO and SO increased by 305% and 124%, respectively, when the concentration of PRE was 20 wt%. Therefore, environmentally friendly multifunctional additive of PRE may be a potential alternative to the traditional additives in the preparation of eco-friendly bio-based lubricant.

Mineral adsorbents, such as talc, are materials that are abundant in nature and used as scavengers, binding agents, fillers, etc. Mechanical and physicochemical pretreatment creates new opportunities for the production of highly effective mineral materials with a wide range of destinations. The possibility of using various techniques to enhance the adsorption properties of dispersed talc, namely, enrichment and use in a mixture with another mineral, treatment with various reagents, and changing the temperature and acidity conditions, is demonstrated. Phenomena and trends having an effect on the adsorption ability of talc are considered. Surface modification of talc can significantly increase its technological capability of absorbing resinous components of wood pulp in the manufacture of paper. It is shown that the adsorption and structural characteristics of dispersed talc change significantly after modifying it with organic reagents. The best effect is achieved when pretreating talc with cationic surfactant N-cetylpyridinium chloride. The resulting adsorbent is characterized by a high value of rosin adsorption, reaching 200 mg/g, which is commensurate with the data on the absorption of rosin by talc pretreated with a Penta-416 industrial mixture. Substantial changes in the surface properties due to an increase in the temperature, a change in the acidity, and a shift in the hydrophilic-hydrophobic balance occur when using the accessible, affordable, and safe anionic surfactants. The highest value of adsorption of rosin (160–170 mg/g) is typical for samples of talc modified with sodium oleate and enriched with zinc oxide. The importance of pretreatment of talc with solutions of mineral acids and salts that promote settling of suspensions and the formation of a compact precipitate is shown.

It is of great significance to explore novel applications of renewable resources. In this study, a rosin-based anionic surfactant (abbreviated R-11-2-Na), which contains a large hydrophobic group of 30 carbon atoms, was synthesized. R-11-2-Na forms wormlike micelles in the presence of the equimolar organic salt choline chloride, endowing solutions with strong viscoelasticity. The wormlike micellar solutions were investigated using rheology, small-angle X-ray scattering, and freeze-fracture transmission electron microscopy (FF-TEM) methods at 25 °C. Due to the strong van der Waals interactions caused by the large hydrophobic group contained in R-11-2-Na, the zero-shear viscosity (η0) of solutions showed extremely strong dependence on the concentration with an exponent of 23.4. The cross-sectional diameter of the wormlike micelles in the present system was significantly larger than that of the wormlike micelles formed by surfactants containing conventional alkyl tails. This finding may be attributed to the steric hindrance brought by the bulky and rigid dehydroabietic acid unit in the hydrophobic part. The wormlike micelles also showed high tolerance to the organic salt concentration. The present study reveals the notable qualities of rosin-based derivatives in forming complex fluids and facilitates new utilizations of forest resources.

Biologically derived polymers are a very attractive subject for investigation, due to the strict pro-ecological requirements imposed by developed countries, including zero-waste and zero-carbon policies as well as volatile organic compound (VOC) limits. Synthesis of biologically-derived polyesters from natural rosin and bio-diols, showing softening temperatures suitable for application in VOC-free paints and varnishes, was performed to create a desired, future commercial product, that meet the aforementioned requirements regarding VOC and elimination of petroleum-based raw materials. Prepared polymers were used in the formulation of coating materials whose properties: cross-linking behavior, glass transition temperature, thermal stability, storage modulus, hardness, cupping resistance, adhesion, chemical resistance, gloss, haze, color, and anti-corrosive behavior in the salt chamber were investigated and discussed. As a result, coatings with prepared bio-polyesters contained over 80 wt.% of natural resources and showed competitive/better properties than petroleum-based references. They can be applied in the prototyping of “green” powder paints for the protection of steel substrates from corrosion and aggressive solvents.

The method of transferring graphene to semiconductor substrates based on rosin gradually becomes common in practice. Unlike the previous method (use of polymethacrylate) this procedure does not lead to significant contamination at the end of the transfer. The disadvantage, however, is the need to use two solvents: acetone and banana oil instead of one. The purpose of this article is to investigate, by means of a planned experiment, the influence of rosin solvents conventionally used on the resulting graphene layer contamination. The solvents used were isopropyl alcohol (IPA), ethanol and xylene. It was shown by the measured data using atomic force microscopy (AFM), that the lowest contamination can be achieved using isopropyl alcohol.

[EN] Completely biobased and biodegradable thermoplastic starch (TPS) based materials with a tunable performance were prepared for food packaging applications. Five blends were prepared by blending TPS with 10 wt%. of different pine resins derivatives: gum rosin (GR), disproportionated gum rosin (RD), maleic anhydride-modified gum rosin (CM), pentaerythritol ester of gum rosin (LF), and glycerol ester of gum rosin (UG). The materials were characterized in terms of thermo-mechanical behavior, surface wettability, color performance, water absorption, X-ray diffraction pattern, and disintegration under composting conditions. It was determined that pine resin derivatives increase the hydrophobicity of TPS and also increase the elastic component of TPS which stiffen the TPS structure. The water uptake study revealed that GR and LF were able to decrease the water absorption of TPS, while the rest of the resins kept the water uptake ability. X-ray diffraction analyses revealed that GR, CM, and RD restrain the aging of TPS after 24 months of aging. Finally, all TPS-resin blends were disintegrated under composting conditions during the thermophilic incubation period (90 days). Because of the TPS-resin blend's performance, the prepared materials are suitable for biodegradable rigid food packaging applications., This research was funded by MINECO, with the project: PROMADEPCOL: MAT2017-84909-C2-2-R.

The aim of this study was to get a better understanding of the formulation aspect of a new linseed oil – rosin varnish inspired by the antique violin coating, using heat-treated and non-treated rosin. To do so, the heat treatment effect on rosin was studied on both its thermal properties and some of the varnish properties. The rosin without heat treatment was assigned as the reference. The temperature treatments were: 180 °C, 200 °C and 250 °C. The thermal properties were studied using TMA, DSC, ATG and HPLC. A change due to heat treatment was observed, especially on the softening point and the glass transition, which increase with the temperature. Chemical changes were observed, with the apparition of dehydrogenated and oxidised forms of abietane-based acid, which are not present in the reference rosin. As expected, the amount of turpentine decreases with the heat treatment. The varnish properties are also impacted, with a decrease of brightness and solvent resistance with the temperature. A PCA was made in order to have a statistical analysis of the results. Through this, a clear separation of the four groups was graphically observed, with different representative variables. The variables' influence on each other was also clearly identified, as well as the impact of the chemical changes on thermal and varnish properties.

We report on gelatin films incorporating rosin-grafted cellulose nanocrystals (r-CNCs), which fulfill the most relevant requirements for antimicrobial packaging applications. Transparent gelatin/r-CNCs bionanocomposite films (0.5–6 wt% r-CNCs) were obtained by solution casting and displayed high UV-barrier properties, which were superior to the most used plastic packaging films. The gelatin/r-CNCs films exhibited a moderate water vapor permeability (0.09 g mm/m2 h kPa), and high tensile strength (40 MPa) and Young's modulus (1.9 GPa). The r-CNCs were more efficient in improving the optical, water vapor barrier and tensile properties of gelatin films than conventional CNCs. Grafting of rosin on CNCs resulted in an antimicrobial nanocellulose that inhibited the growth of Staphylococcus aureus and Escherichia coli. The antibacterial properties of r-CNCs were sustained in the gelatin films, as demonstrated by agar diffusion tests and proof-of-principle experiments involving cheese storage. Overall, the incorporation of r-CNCs as active fillers in gelatin films is a suitable approach for producing novel eco-friendly, antimicrobial packaging materials., This research was made possible thanks to the facilities of the Laboratory of Pulp and Paper 479 Science and Graphic Arts (LGP2) that is part of the LabEx Tec 21 (Investissements d'Avenir - grant 480 agreement n°ANR-11-LABX-0030) and of PolyNat Carnot Institute (Investissements d'Avenir - 481 grant agreement n° ANR-16-CARN-0025- 0), and Plant Macromolecule Research Center 482 (CERMAV) for the support to this work. This study was financed in part by CNPq, SISNANO 26 483 (MCTI), FINEP, Embrapa AgroNano research network (Embrapa), Coordenação de 484 Aperfeiçoamento de Pessoal de Nível Superior - Brazil (CAPES) [Finance Code 001] and by the 485 São Paulo Research Foundation (FAPESP) [grant numbers 2016/03080-2, 2017/18725-2 and 486 2018/00278-2, 2018/10899-4, 2018/22214-6, 2018/18953-8]. We would like to thank Berthine 487 Khelifi , Cécile Sillard and Thierry Encinas from Grenoble Institute of Technology for their 488 expertise in providing SEM imaging, XPS and XRD analyses, respectively.

Green nanocomposites from rosin-limonene (Ros-Lim) copolymers based on Algerian organophilic-clay named Maghnite-CTA+ (Mag-CTA+) were prepared by in-situ polymerization using different amounts (1, 5 and 10% by weight) of Mag-CTA+ and azobisisobutyronitrile as a catalyst. The Mag-CTA+ is an organophilic montmorillonite silicate clay prepared through a direct exchange process, the clay was modified by ultrasonic-assisted method using cetyltrimethylammonuim bromide in which it used as green nano-filler.The preparation method of nanocomposites was studied in order to determine and improve structural, morphological, mechanical and thermal properties ofsin.The structure and morphology of the obtained nanocomposites(Ros-Lim/Mag-CTA+) were determined using Fourier transform infrared spectroscopy, X-ray diffraction, scanning electronic microscopy and transmission electronic microscopy. The analyses confirmed the chemical modification of clay layers and the intercalation of rosin-limonene copolymer within the organophilic-clay sheets. An exfoliated structure was obtained for the lower amount of clay (1% wt of Mag-CTA+), while intercalated structures were detected for high amounts of clay (5 and 10% wt of Mag-CTA+). The thermal properties of the nanocomposites were studied by thermogravimetric analysis (TGA) and show a significant improvement inthe thermal stability of the obtained nanocomposites compared to the purerosin-limonene copolymer (a degradation temperature up to 280 &deg, C).

Marine biofouling can cause a biocorrosion, resulting in degradation and failure of materials and structures. In order to prevent sea creatures from attaching to the surface, in this work, a new environmentally friendly antifouling coating by incorporating antibacterial polymers and natural antifouling agents has been designed and synthesized. Surface chemical composition and changes in surface hydrophobicity were studied by FTIR spectroscopy and contact angle measurements, respectively. Measurements of mass loss of antifouling resin were also carried out and the release rate of camphor from antifouling coating was tested by using UPLC. It had been found that the changes in the content of triisopropylsilylacrylate (TIPSA) (from 4% to 12%) and isobornyl methacrylate (IBOMA) (from 50% to 16.7%) did not significantly affect the release of camphor. The content of IBOMA decreased from 50% to 16.7%, the antifouling performance of the resin system appeared slightly reduced. In addition, rosin could help regulate the release rate of the resin system to desorb camphor slowly in water in a controlled manner. Furthermore, the antifouling capability of as-prepared samples was evaluated via algae suppression experiments and marine field tests. This study highlighted the environmentally friendly antifouling coating as a potential candidate and efficient strategy to prohibit biofouling in seawater.

Exploration of novel molecular aggregates that stabilize foam systems is helpful to optimize foam properties. Herein, solutions of a rosin-based low-molecular-weight hydrogelator, abbreviated as R-6-AO, were used to generate foams above the critical gelation temperature (Tgel). The foams with R-6-AO concentrations above the critical gelation concentration were very stable below Tgel. The high stability of the foams under such conditions was attributed to the self-assembly of nanoscale fibers of R-6-AO in the liquid films of the foams, leading to extremely slow drainage of water. The foams showed strong water retention and were classified as very wet foams. For example, the foams generated from 10 mM (0.44 wt%) R-6-AO solution subjected to a fast cooling process contained about 45 vol% trapped water after 2000 min. In comparison, the water volume fraction of a 10 mM sodium dodecyl sulfate (SDS) foam decreased from 20 vol% to 1 vol% within 18 min. Because the growth, elongation, and cross-linking of the assembled nanofibers in the liquid films were affected by the cooling process, the stability of these foams also depended on the initial preparation temperature. The present system reveals the importance of microstructures in regulating foam behavior and serves as a new type of condition-sensitive intelligent foam.