The effect of alkali pre-treatment on formation and adsorption of silver nanoparticles on cotton surface

This study is an attempt to investigate the feasibility of alkali pre-treatment to activate surface hydroxyl groups of cellulose fibers in order to enhance the deposition efficiency of silver nanoparticles (AgNPs) onto cotton fabrics. Cotton samples were pre-treated with various alkali solutions containing different earth metal hydroxides (LiOH, NaOH, and KOH). The as-prepared samples were then treated with aqueous silver nitrate followed by reduction treatment with aqueous ascorbic acid, which caused in situ formation of AgNPs on fiber surfaces. The surface structure of the fabrics was characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD) analysis, and colorimetric data. The amount of silver was measured by using inductively coupled plasma-optical emission spectrometer (ICP-OES). Antimicrobial activity was measured against Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli bacteria. It was established that alkali pre-treatment had a substantial effect on the formation and adsorption of AgNPs on the fibers. Alkali pre-treated samples were homogeneously coated by AgNPs with high surface coverage. Alkali type had significant effect not only on the amount of AgNPs on the surface but also on its size. High antibacterial activity against both Gram-positive and Gram-negative strains was also demonstrated, even after 10 cycles washing.     

Effect of surface treatment of jute fibers on the interfacial adhesion in poly(lactic acid)/jute fiber biocomposites

Jute fibers have immense potential to be used as natural fillers in polymeric matrices to prepare biocomposites. In the present study jute fibers were surface treated using two methods: i) alkali (NaOH) and ii) alkali followed by silane (NaOH+Silane) separately. Effects of surface treatments on jute fibers surface were characterized using fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM) analyses. Further, the effects of surface treatments on jute fibers properties such as crystallinity index, thermal stability, and tensile properties were analyzed by X-ray diffraction method (XRD), thermo gravimetric analysis (TGA), and single fiber tensile test respectively. The effects of surface treatment of jute fibers on interphase adhesion between of poly(lactic acid) (PLA) and jute fibers were analyzed by performing single fiber pull-out test and was examined in terms of interfacial shear strength (IFSS) and critical fiber length.     

Surface modification of cellulose fibers by layer-by-layer self-assembly of lignosulfonates and TiO2 nanoparticles: Effect on photocatalytic abilities and paper properties

Depositing of TiO₂ nanoparticles on cellulose fiber surface has potential technological applications in the field of photocatalysis. With this motivation, multilayers composed of lignosulfonates (LS) and TiO₂ nanoparticles were constructed on cellulose fiber surface via layer-by-layer (LBL) self-assembly technique. X-ray photoelectron spectroscopy (XPS), zeta potential measurement and atomic force microscopy (AFM) were used to characterize the LS/TiO₂ multilayers on cellulose fiber surface. Moreover, the photocatalytic activities of modified cellulose fibers (decomposition of methyl orange and antibacterial test) were investigated. The decomposition efficiency of methyl orange for a (LS/TiO₂)₅ multilayer modified cellulose fibers was 74.7 % under 5 h UV irradiation. Photocatalytic decomposition efficiency of methyl orange by LS/TiO₂ multilayer modified cellulose fibers under the same UV irradiation time increased linearly with the number of bilayers. Antibacterial tests results revealed that the cellulose fibers modified with LS/TiO₂ multilayers exhibited excellent antibacterial activity against E.coil. The degree of E.coil growth inhibition for a (LS/TiO₂)₅ multilayer modified cellulose fiber reached as high as 93 %. In addition, the effect of LS/TiO₂ multilayers on properties of handsheets made from modified cellulose fibers was also considered. The air permeability of the handsheet prepared from fibers modified with TiO₂/LS multilayers had 6.1–24.3 % higher compared with that of handsheet prepared from original fibers. The wetting properties measurement results demonstrated that the water contact angle of handsheet oscillated with the increasing number of layers depended on building block which was in the outermost layer.     

Surface modification of polyester fibers by thermal reduction with silver carbamate complexes

In this study, the surface of polyester fiber was modified by means of thermal treatment with a silver carbamate complex. We used scanning electron microscopy (SEM), an X-ray diffraction technique (XRD), and X-ray photoelectron spectroscopy (XPS) to allow a detailed characterization of the silver-coated polyethylene terephthalate (PET) fibers. The results revealed remarkable changes in the surface morphology and microstructure of the silver film after thermal reduction. On SEM, the silver nanoparticles (AgNPs) were seen to be uniformly and densely deposited on the fiber surface. The XRD pattern of the silver-coated fiber indicated that the film has a crystalline structure. A continuous layer of AgNPs, between 30 and 100 nm in size, was assembled on the PET fibers. The PET/Ag composite was found to impart high conductivity to the fibers, with an electrical resistivity as low as 0.12 kΩ·cm.     

Effect of surface treatment on the structure and properties of para-aramid fibers by phosphoric acid

The surface of para-aramid fiber was modified by phosphoric acid solutions (H3PO4) based on an orthogonal experimental design and analysis method. Statistical results indicate that treatment temperature is the most significant variable in the modification processing, while treatment time was the least important factor. The structure and morphology of the modified fiber were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction instrument (XRD), and scanning electron microscope (SEM). The results showed that some polar groups were introduced into the molecular structure of aramid fibers and the physical structure of the treated fibers was not etched obviously. The interfacial properties of aramid fiber/epoxy composites were investigated by the single fiber pull-out test (SFP), and the mechanical properties of aramid fibers were investigated by the tensile strength test. The results showed that the interfacial shear strength (IFSS) of aramid/epoxy composites was remarkably improved and the breaking strength of aramid fibers was not affected appreciably after surface modification.     

Effect of monophenyl borate on properties of high-ortho phenolic fibers

A series of monophenyl borate (MPB) modified high-ortho phenolic copolymer fibers (BOPFs) were prepared by melt-spinning of the high-ortho phenol-formaldehyde resins with different content of MPB, and cured in a formaldehyde solution. The solution curing fibers were heated up to 240 °C at elevated temperatures in N₂. The effect of MPB on the structure and properties of the BOPFs was investigated by Fourier transform infrared spectrometer (FTIR), nuclear magnetic resonance spectroscopy (NMR), thermogravimetric analysis (TGA) and scanning electron microscope (SEM). The results show that a B-O linkage inserts into the high-ortho phenolic copolymer molecular chain with the addition of MPB, and increases the crosslinkage and thermal stability. The peak of O/P (ortho/para) value of fiber (1.94) and elongation (5.6 %) were obtained when BOPFs-4 was heat-cured at 240 °C for 2 h.     

Synthesis and characterization of cellulose carbamate by liquid-solid phase method

An efficient and environmentally friendly method for the synthesis of cellulose carbamate from a mixture of cellulose pulp or the activated cellulose pulp and urea was presented in this paper. Cellulose carbamate with a nitrogen content of 1.21 % and 3.29 % were successfully synthesized via esterification reaction in the high-boiling aprotic and polar N-methyl-2-pyrrolidone solvents (hereinafter NMP). The structures of cellulose carbamate were characterized by Fourier transform infrared spectroscopy (FTIR), Kjeldahl analysis, thermo-gravimetric analysis, scanning electron microscopy (SEM), X-ray diffractometry (XRD), and ¹³C-solid-state NMR. The results showed that some functional groups of the alkali cellulose were substituted by amino in the high-boiling aprotic and polar solvents, then the cellulose carbamate was prepared with the reduced crystallinity and thermal decomposition temperature. In addition, the product was prepared with uniform substitution and distribution of carbamate group in the cellulose chain, which guaranteed its good solubility in aqueous alkali as well as its spinnability to produce fiber.     

Modification of polyacrylonitrile precursor fiber with hydrogen peroxide

Polyacrylonitrile (PAN) precursor fibers were modified for different periods of time using hydrogen peroxide aqueous solution. A variety of tests were employed to characterize the fibers. The modification could induce cyclization and oxidation in the precursor fibers, as reflected by the changes in length and diameter of the fibers, and the results of Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Compared with the unmodified fiber, the modified fibers released less heat during a heating process similar to stabilization of PAN precursor fiber. Also, the modified fibers showed lower characteristic temperatures on differential scanning calorimetry (DSC) thermograms, and lower onset temperature of weight loss on thermal gravimetry (TG) curves. The modified fibers had more surface defects and hence exhibited lower tenacity and tensile modulus. Compared with the unmodified fibers, however, the modified fibers had smoother surface and fewer defects after stabilization. The strain decreased with increasing temperature under a constant tension for all the fibers. At the temperatures above 200 °C, the shrinkage of the fibers decreased with the increase of modification time, because a certain degree of cyclization and oxidation occurred in modified fibers, making them shrink less in the temperature range equivalent to stabilization.     

Effect of Chemical Modifications on Surface Morphological,Structural, Mechanical,and Thermal Properties of Sponge-gourd Natural Fiber

Sponge-gourd (SG) natural fibers obtained from Luffa cylindrica plant were chemically treated separately using alkali (5, 10, and 15 wt%), acetic anhydride (5, 10, and 15 wt%), and benzoyl chloride (5, 10, and 15 wt%). Both untreated and chemically treated SG fibers (SGFs) were subsequently characterized using a field emission scanning electron microscope, a Fourier transform infrared spectrometer, an X-ray diffractometer, a universal testing machine, and a thermogravimetric analyzer. Surface analysis by scanning electron microscopy shows that the alkali treatments promote better outer surface layer than other treatments of the SGF with the exposition of inner fibrillar structure, thereby increasing roughness of the fiber surface. Alkali treatment also improves the crystallinity and exhibits new chemical bond formation in the SGF. The tensile strength and Young’s modulus have been analyzed through a two-parameter Weibull distribution model, where a significant increase in mechanical property of benzoylated fibers has been observed. The thermal stability of the modified fibers is also found to increase by acetic anhydride treatment.     

Preparation,structure and properties of boron modified high-ortho phenolic fibers

Boron modified high-ortho phenolic fibers (o-BPFs) were prepared by melt-spinning from boron modified highortho phenolic resins (o-BPRs) with the weight-average molecular weight of 4973 g/mol, followed by being cured in a solution of formaldehyde and hydrochloric, and then heat-treated under high temperature. Gel permeation chromatography (GPC) and nuclear magnetic resonance spectroscopy (NMR) were used to measure the average molecular weight and ortho/para (o/p) ratio of o-BPRs. Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) were used to characterize the chemical and morphological structures of o-BPRs and o-BPFs. Thermogravimetric analysis (TGA) was employed to examine the thermal stability properties of different resins and fibers and the tensile strength of fibers was measured by a tensile tester. It was found that under proper curing and heat-treatment conditions, the tensile strength of o-BPFs reached 213.6 MPa and the char yield in N₂ atmosphere at 800 °C attained 75.4 %. Compared with phenolic fibers (PFs), the decomposition temperatures at 5 % weight loss of o-BPFs in N₂ and air atmospheres were increased by 156.8 °C and 219.0 °C, respectively.     

不同预处理方法对油茶籽种皮成分、结构和抗氧化活性的影响

油茶籽种皮富含多种活性成分,本文通过探讨不同预处理方法对油茶籽种皮成分、结构和抗氧化活性的影响,为实现油茶籽种皮变废为宝和深加工利用提供科学依据.对比了酸法、碱法、亚临界水和离子液体4种预处理方法所得海南油茶籽种皮中的总酚含量、纤维素组成,并运用扫描电镜(SEM)、X-射线衍射(XRD)、傅里叶变换红外光谱(FTIR)...     

Thermal conductivity and thermal expansion behavior of pseudo-unidirectional and 2-directional quasi-carbon fiber/phenolic composites

In the present paper, a variety of fiber reinforcements, for instance, stabilized OXI-PAN fibers, quasi-carbon fibers, commercial carbon fibers, and their woven fabric forms, have been utilized to fabricate pseudo-unidirectional (pseudo-UD) and 2-directional (2D) phenolic matrix composites using a compression molding method. Prior to fabricating quasi-carbon fiber/phenolic (QC/P) composites, stabilized OXI-PAN fibers and fabrics were heat-treated under low temperature carbonization processes to prepare quasi-carbon fibers and fabrics. The thermal conductivity and thermal expansion/contraction behavior of QC/P composites have been investigated and compared with those of carbon fiber/phenolic (C/P) and stabilized fiber/phenolic composites. Also, the chemical compositions of the fibers used have been characterized. The results suggest that use of proper quasi-carbonization process may control effectively not only the chemical compositions of resulting quasi-carbon fibers but also the thermal conductivity and thermal expansion behavior of quasi-carbon fibers/phenolic composites in the intermediate range between stabilized PAN fiber- and carbon fiber-reinforced phenolic composites.     

Modification of enzyme pretreated cotton fabric using acrylonitrile, acrylonitrile/solvent mixture and its characterization

The presented research deals with modifying the chemical structure of the bioscoured cotton fabric by acrylonitrile, acrylonitrile/acetone, and acrylonitrile/ethanol mixture. The modified cellulose was tested for weight gain, shrinkage, and wicking height and characterized by X-ray diffraction (XRD), thermal analysis (TG/DTA), elemental analysis, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The weight gain and shrinkage % show increased value for modified fabrics. The wicking height increases with addition of solvent. The crystallinity and thermal studies show a significant change. FTIR analysis confirms the modification by the occurrence of -C??N stretching and -CONH₂ stretching. The SEM morphology of modified fabric shows uniform swelling of fibers with better smoothness. The AFM topography reveals that the addition of solvent affects the particle size. Clear surface morphology of modified fabric reveals that this processing method can be used for preparation of medical textiles with more swelling.     

Surface treatments of jute fabric: The influence of surface characteristics on jute fabrics and mechanical properties of jute/polyester composites

In this study, jute fabrics were modified by alkali, micro-emulsion silicon (MS) and fluorocarbon based agents (FA) in order to enhance the interfacial adhesion between the polyester matrix and the jute fiber. X-ray photoelectron spectroscopy (XPS) and contact angle measurements were used to characterize fiber surfaces. The effects of various surface treatments on the mechanical and morphological of jute/polyester composites were also studied. All surface treatments were shown to improve the tensile, flexural strengths and interlaminar shear strengths of the composites. Moreover, the maximum improvement in the mechanical properties was obtained for the FA treated jute/polyester composites. SEM micrographs of the tensile fracture surface of jute/unsaturated polyester composites also exhibited improvement of interfacial and interlaminar shear strengths by the alkali, MS and FA treatments of jute fibers.     

菠萝叶纤维素均相酯化改性制备甲醛气体净化材料

以菠萝叶纤维为原料,采用均相酯化取代反应制备了改性纤维素甲醛净化材料。以氯化血红素为催化剂、DMSO/LiCl为溶剂,在均相条件下对菠萝叶纤维素进行酯化取代改性反应。系统考察了反应条件对纤维素酯化效率的影响,改性后的菠萝叶纤维素的酯化效率为15.64%,并且其对甲醛降解效果最好。对改性前后的菠萝叶纤维素进行扫描电镜(SEM)、红外光谱(FT-IR)、热重分析(TGA)和比表面积(BET)分析,发现改性纤维素表面出现大量颗粒状物质;有氯化血红素的吸收峰出现;改性纤维素的比表面积显著提高,有利于吸附甲醛;热分解温度降低、最终残留物比例较高,说明了发生了酯化取代反应。     

Properties of flame-retardant cellulose fibers with ionic liquid

Flame-retardant cellulose fibers were prepared by dissolving cellulose in tetrabutylammonium acetate and dimethyl sulfoxide, and blending with amino silicone oil (ASO). The ASO was used as a novel fabric softener and flame retardant for cellulose fibers. Fourier-transform infrared spectroscopy showed that blending with ASO did not adversely affect the cellulose fibers. The flame retardancy of the cellulose fibers blended with ASO was determined based on the limiting oxygen index (LOI). Cellulose fibers blended with 8 wt% (add-on) ASO gave the best flame retardancy, with an LOI of 28, which was higher than that of the virgin fibers. The thermal properties of the flame-retardant cellulose fibers were investigated using differential scanning calorimetry and thermogravimetric analysis. The results showed that ASO prevented degradation of the cellulose fibers, hindered the formation of volatile species, and favored char formation. The mechanical properties of the flame-retardant cellulose fibers were better than those of virgin cellulose fibers.     

添加酶制剂对饲用苎麻与麦麸混合青贮品质的影响

为了探究酶制剂对苎麻混合青贮品质的影响,本试验在苎麻与麦麸(80%苎麻+18%麦麸+2%蔗糖)混合青贮中分别添加10 mL蒸馏水(对照组)、纤维素酶2 g/kg、纤维素酶2 g/kg+半纤维素酶0.4 g/kg、纤维素酶2 g/kg+半纤维素酶0.4 g/kg+果胶酶0.7 g/kg,30天后开包取样分析各项指标。结果表明,苎麻与麦麸混合青贮发酵品质和营养品质均较好。与对照相比,添加酶制剂显著提高了碳水化合物、干物质和粗蛋白含量(P<0.05),显著降低了中性洗涤纤维、酸性洗涤纤维、粗纤维的含量和氨态氮/总氮比值(P<0.05),但是对pH值、乳酸、乙酸和丙酸含量无显著影响(P<0.05)。本试验条件下,添加酶制剂能够有效提高苎麻混合青贮的品质,单独添加纤维素酶与复合酶制剂无显著性差异,从节约成本角度考虑,单独添加纤维素酶组为最佳选择。     

Effect of kenaf and EFB fiber hybridization on physical and thermo-mechanical properties of PLA biocomposites

Kenaf/empty fruit bunch/polylactic acid (kenaf/EFB/PLA) hybrid biocomposites were prepared using hot press technique. The ratio of fiber to polylactic acid was set at 60:40 with 1:1 ratio between kenaf and empty fruit bunch fibers. Physical, mechanical and thermal properties of hybrid biocomposites were subsequently characterized using Fourier transform infrared spectroscopy, scanning electron microscope, X-ray diffraction, thermogravimetric analysis, differential scanning calorimetry, tensile and water absorption tests. Test results indicated that mechanically stronger fiber was able to support the weaker fiber. Hybrid fiber biocomposite had higher crystallinity as compared to single fiber biocomposite. Water absorption of hybrid composite was higher as compared to single fiber composite. Thermal result revealed that hybridization of fiber was not significantly influence the thermal properties of composites. However, the presence of two different fibers proposed good wettability properties, which could reduce the formation of voids at the fibers-polymer interface and produce composites with high stiffness and strength.     

Surface modifications of natural Kanchipuram silk (pattu) fibers using glow discharge air Plasma

Experimental investigations have been carried out to modify the surface properties of natural Kanchipuram silk (pattu) fibers using a low temperature DC glow discharge air Plasma. Silk is an externally spun fibrous protein secretion formed into fibers. Plasma treatment is an eco-friendly, dry, and clean process over wet chemical method and does not suffer from any environmental and health concerns. Experiments have been performed considering three parameters such as discharge current, treatment time, and working pressure. The structural, thermal, morphological, optical, and mechanical studies of raw and plasma treated silk fibers have been obtained out using attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) spectroscopy, X-ray diffraction (XRD), thermo gravimetric analyzer (TGA), scanning electron microscope (SEM) with energy dispersive spectroscopy (EDS), diffuse absorbance spectroscopy, and tensile test. A comparative study has been done for the untreated and different treated fibers. Various characterization analyses reveal that surface roughness of the plasma treated silk fiber is increased and also crystallite size of treated samples is enhanced, plasma treated silk fibers maintain the whiteness effect and it is observed that UV transmittance region (A & B) is more for the treated fiber which signifies enhanced UV protection.     

Effect of chemically modified date palm leaf fiber on mechanical,thermal and rheological properties of polyvinylpyrrolidone

Polyvinylpyrrolidone/date palm leaf fiber (PVP/DPL) biocomposites were prepared by melt mixing fabrication technique with different weight percentage of fibers. DPL fibers were chemically modified by acrylic acid in order to have better dispersion and compatibility with PVP matrix. The interaction of DPL fibers with PVP matrix was studied by Fourier transforms infrared spectroscopy (FTIR). Field emission scanning electron microscope (FESEM) was used for the study the morphology of chemically modified DPL fibers and PVP/DPL biocomposites. Mechanical properties were improved with fiber loading due to strong interfacial adhesion between PVP and DPL fibers. The storage modulus, loss modulus and tan delta values of PVA/DPL biocomposites were measured by DMTA. The rheological properties were investigated to study the shearing storage and loss modulii along with complex viscosity of biocomposites. The thermal and conducting properties of biocomposites were measured and compared with that of virgin PVP.