Effect of alkali and ultraviolet (UV) radiation pretreatment on physical and mechanical properties of 1,6‐hexanediol diacrylate–grafted jute yarn by UV radiation

To improve the physicomechanical properties of jute yarn, grafting with 1,6‐hexanediol diacrylate (HDDA) monomer was performed by a UV radiation technique. A series of HDDA solutions of various concentrations in methanol were prepared. A small quantity of photoinitiator (Darocur‐1664) was also added to HDDA solutions. To optimize the conditions for grafting, the effects of monomer concentration, soaking time, and radiation doses were studied by varying the number of soaking times along with variation of monomer concentrations and UV radiation intensities. The extent of polymer loading and the mechanical properties like tensile strength (TS), elongation at break (Eb), and tensile modulus of both treated and untreated jute were investigated. The highest tensile strength, polymer loading, and modulus were achieved with 5% HDDA concentration, 5 min soaking time, and the 4th pass of UV radiation. This set of conditions was selected as optimum and produced enhanced tensile strength (67%), modulus (108%), and polymer loading (11%) over those of virgin fiber. To further improve the mechanical properties the jute yarns were pretreated with alkali (5% NaOH) solution and after that the alkali‐treated yarn were treated under UV radiation of various intensities. The pretreated samples were grafted with optimized monomer concentration (5% HDDA). Increased properties of alkali + UV‐pretreated and grafted samples such as polymer loading (12%), tensile strength (103%), elongation at break (46%), and modulus (114%) were achieved over those of virgin jute yarn. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 18–24, 2004     

Role of Amino Acids on In Situ Photografting of Jute Yarn with Acrylamide Using Ultraviolet Radiation

Abstract

To improve the mechanical performance of jute yarn, grafting with acrylamide (AM) monomer has been performed on in situ UV radiation and optimized; the monomer concentration (30%) and irradiation time (60 min) attained 195% tensile strength with 22% polymer loading (PL). The effect of amino acids (1%) as additives in AM with photografted jute yarn at optimized system has been studied. The PL and tensile properties, such as tensile strength (TS) and elongation at break (Eb), of treated samples were enhanced by incorporation of amino acids, and the highest TS value (270%) and Eb value (300%) with 27% PL value were achieved by the sample treated with L‐arginine (Arg). Weak acid [3% acetic acid (Ace)] and strong acid [1% sulfuric acid (Sul)] were also incorporated in the optimized system of AM grafting to investigate their effect on the mechanical properties of photografted jute yarn. Water absorption and weathering resistance of treated untreated samples (TS₀) were also studied.     

Effect of Pretreatment with Ultraviolet Radiation on the Physicomechanical Properties of Photocured Coir (Cocos nucifera) Fiber with 1-Ethyl-2-Pyrrolidone (1-E-2-P) Monomer

Coir fiber (Cocos nucifera) was modified with 1-ethyl-2-pyrrolidone (1-E-2-P) monomer by photocuring. A series of formulations of different concentration of 1-ethyl-2-pyrrolidone (3, 5, 10, 20, 30, and 70%) in methanol was prepared along with 2% photoinitiator (Darocur-1664). Concentration of 1-E-2-P, soaking time, and radiation doses were optimized and found that 5% 1-E-2-P, 7 min soaking time, and 5th pass of UV radiation was the optimized condition that gave the maximum values as polymer loading (PL) (21%) and 71% higher tensile strength over virgin one. The coir fiber was pretreated with ultraviolet (UV) radiation of various intensities for further improvement of mechanical properties. The mechanical properties, such as TS (tensile strength), Eb (elongation at break), and modulus (σ) of the pretreated fiber, were monitored. Fiber treated with 130th pass of radiation showed the higher TS, Eb, and σ. The fiber irradiated at 130th pass of UV radiation gave the maximum values as PL (35%) and 74% and 18% higher tensile strength and elongation at break, respectively. The fiber, both treated and untreated, was subjected to water absorption. The pretreated and cured coir fiber showed the minimum water uptake behavior.     

Jute composite with MMA by gamma and UV radiations in the presence of additives

Jute yarns treated with MMA + MeOH solutions were irradiated either with Co‐60 gamma source or with UV radiation. In gamma radiation, polymer loading of MMA (methyl methacrylate) onto jute increased quite substantially, but the strength of the composite decreases sharply after 15% polymer loading. The gamma‐treated jute samples were very brittle. On the other hand, jute yarns irradiated in situ under UV radiation was found to be grafted with MMA. The tensile strength of the UV‐cured jute yarn composite increases with an increase of grafting level, in contrast to the behavior observed with the gamma‐irradiated jute composite samples. The tensile properties of the composites can be further enhanced by the incorporation of certain additives and coadditives into MMA + MeOH solutions. This opens diverse applications for jute materials. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 900–906, 1999     

Effect of Mercerization on Surface Modification of Henequen (Agave fourcroydes) Fiber by Photo-Curing with 2-Hydroxyethyl Methacrylate (HEMA)

Abstract

Henequen fibers were cured under ultraviolet (UV) radiation with 2-hydroxyethyl methacrylate (HEMA) in order to improve the mechanical properties and reduce the water absorption. A series of solutions of different HEMA concentration in methanol along with photoinitiator Irgacure 907 was prepared. The radiation dose, monomer (HEMA) concentration and soaking time were optimized with respect to grafting of monomer and mechanical properties of cured fiber. 3% HEMA, 5 min soaking time, at the ninth pass of radiation, produced higher tensile strength (190%) and elongation at break (195%), than those of the virgin fiber, as well as the highest grafting value (4.2%). For further improvement of the mechanical properties, the fibers were treated with an alkali (KOH) solution of various concentrations for 1 h before curing. 10% alkali-treated fibers showed increased properties, such as grafting (5.4%), tensile strength (300%), and elongation at break (290%) over raw fiber. The treated fiber showed lower water uptake than the untreated ones. The grafted fibers were also characterized by IR and it was observed that HEMA deposited on the fiber surface may react with the cellulose backbone of the Henequen fibers.     

Comparison of mechanical and degradation properties of EG and EGDMA grafted gelatin films

Thin films of gelatin were prepared from gelatin granules in aqueous medium by casting and its mechanical properties like tensile strength (TS), tensile modulus (TM), and elongation at break (Eb %) were studied. Gelatin films were procured with two types of monomers such as 5% ethylene glycol (EG) and 5% ethylene glycol dimethacrylate (EGDMA) to increase the mechanical properties. Five percent of monomer solutions were prepared in MeOH along with 2% photoinitiator; Irgacure-651. Soaking time and UV radiation intensities were optimized with the extent of polymer loading (PL) and the mechanical properties of the cured films. Comparing the properties of EG and EGDMA treated gelatin film, EG showed the best performance. The EG-cured gelatin film with 5?min soaking time showed the highest tensile strength (58.6?MPa) and elongation at break (11.2%). The water uptake was determined for raw film (500.1%), EG grafted gelatin film (375.3%), and EGDMA grafted film (412.9%). The degradation properties in water and soil were determined for the raw and cured gelatin films. It was observed that the raw film degrades more than that of the treated films.     

Jute Reinforced Polymer Composite by Gamma Radiation: Effect of Surface Treatment with UV Radiation

Jute (Hessian cloth) reinforced polymer composites were prepared with a mixture of 2-hydroxy ethyl methacrylate (HEMA) and aliphatic urethane diacrylate oligomer (EB-204), and then cured under gamma radiation. Thick pure polymer films (2 mm thickness) were prepared by using the same monomer and oligomer at different weight ratios, and 500 krad of total gamma radiation dose at 600 krad/hr was selected for the curing of all composites. Total radiation dose, jute content, and monomer concentration were optimized with the extent of mechanical properties. Among all resulting composites, the composite of 38% jute content at monomer:oligomer = 50:50 (w/w) ratios showed the better mechanical properties, such as 108% increase in tensile strength (TS), 58% increase in bending strength (BS), 138% increase in tensile modulus (TM), and 211% increase in bending modulus (BM) relative to pure polymer film. The gel content values were also found to increase with the increase of jute content in the composite. But the elongation at break (Eb) for both tensile and bending was found to decrease with increasing jute content. The best mechanical properties were obtained when jute fibers were pre-irradiated with UV radiation, such as 150% increase in TS, 90% increase in BS relative to polymer film, 19% increase in TS, and 15% increase in BS relative to untreated jute-based composites. A water uptake behavior investigation of the resulting composites was also performed and composites based on UV-treated jute showed the minimum water uptake value.     

A comparative study of gamma and ultraviolet radiation on gelatin film with 2-ethylhexyl acrylate

Gelatin films were prepared from gelatin granules in an aqueous medium by casting. Tensile strength (TS) and elongation at break (Eb%) of the films were found to be 29.2?MPa and 4.9%, respectively. Gelatin films were irradiated under gamma and UV radiation with different doses. Gamma treated gelatin films showed higher TS and Eb% over untreated ones, and even higher than that of the UV treated films. A series of gelatin solutions (formulations) was prepared by blending varying percentages (2–10% by wt) of 2-ethylhexyl acrylate (EHA) and then the films were prepared. Some EHA-blended gelatin films were irradiated under gamma radiation at various doses (50–500?krad) and other films were cured under UV radiation at different intensities (10–30 UV passes). EHA-blended?+?gamma treated gelatin films showed the highest mechanical properties than that of the EHA-blended?+?UV treated films. The degradation properties present in the soil were determined for the pure and treated films. It was observed that EHA-blended?+?gamma treated gelatin film degrades more than that of the EHA-blended?+?UV treated films.     

Role of Urea on the Physico-Mechanical and Degradable Properties of Mercerized and Acid Hydrolyzed Coir (Cocos nucifera) Fibers Photocured with 1,6-Hexanediol Diacylate

Abstract

Coir fibers were modified with 1,6-hexanediol diacrylate (HDDA) by using ultraviolet (UV) radiation. Concentration of HDDA, soaking time, and radiation dose were optimized and found to be 30% HDDA in methanol along with photoinitiator Irgacure-500 (2%) and 120 min of soaking time the better performance registered as the optimum conditions, where polymer loading (PL) was 17% and tensile strength (TS) was 50%. Urea of different concentrations (0.5–2%) was incorporated with 30% HDDA to monitor its effect on the properties and 1% urea produced the enhanced PL (25%) and TS (82%). For the improvement of the properties, the fibers were subjected to surface treatment with alkali (5% potassium hydroxide) at various mercerizing times in hot and normal conditions. Among all the mercerized fibers, fibers treated with hot alkali for 6 h and cured under optimized condition demonstrated the maximum enhancement of PL (35.5%) and TS (130%). The fibers were also subjected to acid hydrolysis for different times with different acid (H₂SO₄) concentrations. Again the effect of urea (1%) on the properties of the pretreated fibers was scrutinized. Water uptake and degradable properties of the treated and virgin fibers were performed.     

Mechanical properties development of sodium alginate films with additives by UV‐radiation processing

To improve mechanical properties of polymer films; sodium alginate (SA) films was prepared with ethylene glycol (EG) and photocured. The formulation was prepared at various concentration with EG and photoinitiator (2%) in methanol. The mechanical properties were optimized in case of monomer (EG) concentration, soaking time, and radiation dose of intensities. The highest polymer loading (PL) was 7.1% and tensile strength (TS) of the film was 37.9 MPa were found for 3 min soaking in 5% EG containing formulation at 20th pass of UV radiation; the highest value (22%) of elongation at break (Eb) was obtained at 1 min soaking time at 15th passes of UV doses. The mechanical properties improvement of the films varied acrylic monomers; such as 2‐ethylhexylacrylate (EHA), 1,4‐butanediol diacrylate (BDDA), and trimethylpropane triacrylate (TMPTA) were used as additives (2%) in the optimized formulation. The highest PL (12.7%) and TS (42.2 MPa) of the films are at 5% EG, 2% TMPTA, and 2% photoinitiator in methanol at 3 min soaking time at 20th pass of UV radiation. The highest Eb (25%) was obtained using additives 2% EHA additives in 5% EG and 2% photoinitiator in methanol at 3 min soaking time. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of pretreatment with detergent on mechanical properties of photocured coir (Cocos nucifera) fiber with ethyleneglycol dimethacrylate

Coir fibers were treated with ethylene glycol dimethacrylate (EGDMA) mixed with methanol (MeOH) under UV radiation. A series of solutions of different concentrations of EGDMA in methanol along with a photoinitator, Irgacure‐500 (mixture of 1‐hydroxylcyclohexylphenylketone and benzophenonc), were prepared. Monomer concentration, soaking time, and radiation intensity were optimized in terms of polymer loading (PL) and mechanical properties. EGDMA (50%), 5 min soaking time at the 4th pass of radiation, produced higher PL and tensile strength (TS), and the values of PL is 17% and TS is 1.3 times of the nontreated one. Then, coir fiber was pretreated with detergent and then treated with the optimized monomer formulation, which exhibited a higher PL of 69% and produced TS of the coir fiber of 4.4 times of the nontreated one. Coir fiber pretreated with detergent along with UV radiation showed the highest TS, which is 18.2 times of nontreated one. Water uptake, degradable properties, and simulated weathering of treated and virgin fibers were also monitored, which showed that EGDMA treatment under UV radiation improved the degradable property. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1630–1636, 2006     

Studies on the Mechanical Properties of Gelatin and Its Blends with Vinyltrimethoxysilane: Effect of Gamma Radiation

Gelatin films were prepared by casting. Tensile strength (TS), elongation at break (Eb) and tensile modulus (TM) of the gelatin films were found to be 56 MPa, 6.1% and 1.14 GPa, respectively. Effect of gamma radiation (Co-60) on the mechanical properties of the gelatin films was studied. Vinyltrimethoxysilane (VTMS) was added to the gelatin during casting varying 1–7% by weight and found to increase the TS and TM significantly. Then the films were irradiated and found further increase of TS and TM. Water uptake of the gelatin films and 5% VTMS containing gelatin films were also evaluated.     

Influence of irradiation crosslinking on the flame-retardant properties of polyolefin blends

In the presence of flame retardants and other additives, halogen-free flame retardant (HFFR) shape-memory polymers were prepared using blends of ethylene vinyl acetate, ethylene propylene diene monomer, and low-density polyethylene. The HFFR compounds were irradiated using electron beam up to an absorbed dose of 150 kGy and characterized based on their mechanical, thermal, and electrical properties. Both the tensile strength (TS) and elongation at break (Eb) were found to increase as the levels of irradiation increased. This contrasted fact that, generally, Eb decreases as radiation doses increases because of polymer crosslinking capability. However, both TS and Eb decreased as the flame retardant content increased. The optimum mechanical properties were 13 MPa for TS and 200–350% for Eb. The versatile glass transition temperature greatly influenced the shape-memory impact. Nevertheless, the variable rubbery modulus had no significant influence. The limiting oxygen index was found to increase as the total flame retardant contents increased to values over the range of 30–35%. Hardness was about 92, and the retentions of TS and Eb after thermal aging at 136 °C for 168 h were between 93–112 and 75–93%, respectively. UL94 ratings of V-0 and a volume resistivity of 3.21 × 10¹⁵ to 3.49 × 10¹⁵ Ωcm were obtained using these HFFR compounds. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48649.     

Improvement of physico-mechanical properties of jute yarn by photografting with 3-(trimethoxysilyl) propylmethacrylate

Jute yarns were treated with an alkoxy silane monomer 3-(trimethoxysilyl) propylmethacrylate under UV radiation. The monomer concentration and radiation intensity were optimized with respect to the extent of grafting and mechanical properties of the grafted (silanized) jute yarn. The enhanced tensile strength by 159%, elongation-at-break (237%) and polymer grafting (26.2%) were observed when the yarn was treated at 30 wt% silane in methanol under UV radiation for 30 min. The surfaces of both treated and untreated jute yarns were characterized by X-ray photoelectron spectroscopy (XPS), Fourier-Transform Infrared Spectroscopy (FTIR) and Environmental Scanning Electron Microscopy (ESEM) and it was concluded that the silane reacted or deposited on jute surface as a result of UV radiation. Water uptake and degradation properties of untreated and silanized jute yarn were studied in various conditions such as simulated weathering and in soil containing 25% water. The silanized jute yarn showed lesser water uptake as well as less weight loss and mechanical properties as compared to virgin samples.     

Mechanical and barrier properties of nanocrystalline cellulose reinforced poly(caprolactone) composites: Effect of gamma radiation

Nanocrystalline cellulose (NCC) reinforced poly(caprolactone) (PCL) composites were prepared by compression molding. The NCC content varied from 2 to 10% by weight. NCC played a significant role in improving the mechanical properties of PCL. The addition of 5 wt % NCC caused a 62% improvement of the tensile strength (TS) value of PCL films. Similarly, tensile modulus (TM) values were also improved by NCC reinforcement but elongation at break (Eb) values decreased montonically with NCC content. The water vapor permeability (WVP) of PCL was 1.51 g·mm/m²·day·kPa, whereas PCL films containing 5 wt % NCC showed a WVP of 1.22 g·mm/m²·day·kPa. The oxygen transmission rate (OTR) and carbon dioxide transmission rate (CO₂TR) of PCL decreased by 19 and 17%, respectively, with 5 wt % NCC incorporation. It was found that the mechanical and barrier properties of both PCL and PCL‐NCC composites further improved with 10 kGy gamma irradiation treatment. The combination of NCC and radiation significantly increased the TS, TM, and Eb (by 156, 123, and 80%, respectively, compared to untreated PCL). The WVP, OTR, and CO₂TR decreased by 25–35% with respect to untreated PCL. The surface and interface morphologies of the PCL‐NCC composites were studied by scanning electron microscopy and suggested homogeneous distribution of NCC within the PCL matrix. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Effect of γ-Radiation on the Mechanical Performance of Hybrid Rice Straw/Seaweed-Polypropylene Composites

Hybrid composites of rice straw (Rs)/seaweed (Sw) and polypropylene (PP) were prepared at a fixed filler ratio of 30:70 and variable ratio of the two reinforcements, viz. 30:0, 25:5, 20:10, 10:20, 0:30 by weight. Mechanical properties of the composites such as tensile strength (TS), bending strength (BS), impact strength (IS) and elongation at break (Eb%) were investigated and the composite formulation of 20:10:70 (Rs:Sw:PP) was found to be optimum that showed TS = 2.8 MPa, BS = 68 N/mm², IS = 2.5 kJ/mm² and Eb = 50%. For better compatibility, Rs and Sw were subjected to surface treatment using various intensities of γ-radiation to prepare improved hybrid composites. γ-irradiated filler hybrid composites significantly enhanced mechanical properties and the composite in which fillers were irradiated at 100 krad achieved maximum enhancement with TS = 35 MPa, BS = 75 N/mm², IS = 2.7 kJ/mm² and Eb = 68%. Water absorption capacity of the different composites was also studied and irradiated filler composites showed less water uptake.     

Photoinitiated surface grafting of synthetic fibers,III. Photoinitiated surface grafting of poly(ethylene terephthalate) fibers

Photoinitiated surface grafting of acrylic acid (AA), acrylamide (AM) and 4-vinyl pyridine (VP) onto poly(ethylene terephthalate) (PET) fibers (a commercial textile yarn) has been studied using benzophenone (BP) as photoinitiator. A continuous process as previously described has been applied, which involves presoaking of the PET yarn in a solution of initiator and monomer in acetone and UV irradiation in nitrogen atmosphere. The resulting grafted polymer on the fiber surface has been analyzed by ESCA, titration of carboxy groups (grafted AA), and dye absorption. The relative ESCA intensities (RI) of O1s/C1s and N1s/C1s are used as measure for grafted AA, AM and VP, respectively, after recording the RI-values for ungrafted fibers. For grafting with AA, the RI-values increased from 32.8% (background) to 48.6% after 20 s irradiation time. The amount of carboxy groups measured by titration increased from 0.045 to 0.106 mmol/m². Assuming an even coverage of grafted AA polymer, this means a grafted layer of 4.8 nm thickness. After grafting, the adsorption of the dye Crystal Violet (CV) from aqueous solution increased by about 3 times. With AM as monomer, the RI-values increased from 2.6 (background) to 14.8% and the adsorption of a direct dye Sirius Lichtbordo B-LL increased by about 6 times. With VP as grafted monomer, the RI-values increased from about 2.6 (background) to 5.1% and the adsorption of the direct dye increased by about 4 times.     

Surface Modification of Sisal (Agavae sisalana) Fiber by Photocuring: Effect of Additives

The sisal fiber (Agavae sisalana) was grafted with methacrylonitrile (MAN) under UV radiation in order to modify its mechanical and degradable properties. A number of MAN solutions of different concentrations in methanol (MeOH) along with photoinitiator Darocur-2959 were prepared. The soaking time, radiation dose and monomer concentration were optimized. Sisal fiber soaked for 60 min in 50% MAN and irradiated at 8th UV pass achieved highest values of tensile properties like tensile strength (TS = 140.2 MPa), and elongation at break factor (Ef = 8) with 8% polymer loading (PL). To further improve the properties of sisal fiber, a number of additives (1%) such as urea (U), polyvinylpyrrolidone (PNVP), tripropelene glycol diacrylate (TPGDA), hexanediol diacrylate (HDDA), trimethyl propane triacrylate (TMPTA), ethylene glycol dimethacrylate (EGDMA) were used in the 50% MAN formulation to graft at the optimized condition. Among the additives used, urea has significantly influenced the PL (9%), TS (190 MPa), and Ef (9) values of the treated sisal fiber. Water uptake and accelerated weathering test were also performed.     

Surface modification of henequen (Agave fourcroydes) fibers by ultraviolet curing with 2‐hydroxyethylacrylate and ethylacrylate: Effect of additives on degradable properties

Henequen fibers were grafted with a double impregnating monomer 2‐hydroxyethylacrylate (HEA) and ethylacrylate (EA) to improve the physicomechanical properties. The fibers soaked in different concentration (1–10%) of monomer + MeOH solution along with photoinitiator Irgacure 907 [2%] were cured under ultraviolet (UV) lamp at different UV radiation intensities (2–14 passes). Concentration of monomer at different radiation intensities was optimized with extent of mechanical properties such as polymer loading, tensile strength, and elongation at break. Enhanced tensile strength (268%) and elongation at break (110%) were achieved by the polymer treated fibers than untreated virgin fibers. We observed that, henequen fibers treated by 3% EA showed better physico‐mechanical properties than those treated by 5% HEA. The tensile properties of henequen fibers treated by 3% EA can be enhanced by adding aloxysilane; 3‐(trimethoxysilyl) propylmethacrylate additives with bulk monomer EA (3%). The degradability of the treated and untreated fibers due to accelerated weathering were also studied and it has been found that surface modified henequen fibers produced more resistivity towards different weathering conditions than untreated fibers. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4000–4006, 2006     

Physico-mechanical and degradation properties of biodegradable photografted coir fiber with acrylic monomers

Coir fibers were modified with 2-hydroxyethyl methacrylate (HEMA), methyl methacrylate (MMA) and 2-hydroxyethyl acrylate (2-HEA) solutions under UV radiation. Monomer concentration and radiation dose were optimized in terms of grafting and tensile properties. It was found that 20 % HEMA at 20th UV pass, 30 % MMA at 15th UV pass and 25 % 2-HEA at 20th UV pass of radiation produced higher tensile properties over untreated sample. Urea of different concentrations (0.5–2 %) were incorporated into optimized solutions and 1 % urea showed the best properties of the fiber. Water uptake behavior and simulating weathering degradation properties were also performed.