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.     

Novel fibers prepared from cellulose in NaOH/thiourea/urea aqueous solution

The regenerated cellulose fibers were prepared by wet-spinning from NaOH/thiourea/urea aqueous solvent system for the first time. The effects of coagulation and stretch conditions on the structure, morphology, and mechanical properties of the prepared fibers were investigated by wide-angle X-ray diffraction (WAXD), scanning electron microscope (SEM), and tensile tester, respectively. When the cellulose spinning dope was coagulated in 10% H₂SO₄/12.5% Na₂SO₄ aqueous solution at 15 °C, the prepared fibers had a typical crystalline structure of cellulose II and circular cross-sectional shapes with smooth surface and slightly high tensile properties to viscose fibers.     

Rheological and thermal properties of acrylonitrile-acrylamide copolymers: Influence of polymerization temperature

An attempt was made to correlate the polymerization temperature and rheological and thermal properties of acrylonitrile (AN)-acrylamide (AM) copolymers. The copolymers were synthesized at different polymerization temperature. The copolymer structure was characterized by gel permeation chromatography (GPC) and Infrared spectrum (IR). The rheological and thermal properties were investigated by a viscometer and differential scanning calorimeter-thermogrametric (DSCTG) analysis, respectively. When the polymerization temperature increased from 41 °C to 65 °C, the molecular weight ([`(M)] <sub>w</sub> )(\overline M _w ) of copolymers decreased from 1,090,000 to 250,000, while its conversion increased from 18% to 63%, and the polymer composition changed slightly. To meet the requirements of carbon fibers, the rheological and thermal properties of products were also investigated. It was found that the relationship between viscosity and [`(M)] _w\overline M _w was nonlinear and the viscosity index (n) decreased from 3.13 to 2.69, when the solution temperature increased from 30 °C to 65 °C. This suggests the dependence of viscosity upon [`(M)] _w\overline M _w is higher at lower solution temperature. According to the result of activation energy, the sensivity of viscosity to solution temperature is higher for AN-AM copolymers synthesized at higher polymerization temperature. The result of thermal analysis shows that the copolymers obtained at higher polymerization temperature are easier to cyclization evidenced from lower initiation temperature. The weight loss behavior changed irregularly with polymerization temperature due to irregular change of liberation heat.     

Modeling and differential evolution optimization of PAN carbon fiber production process

In this research, results of an experimental and artificial neural network fuzzy interface system (ANFIS) modeling of operating parameters on tensile strength of the carbon fibers are investigated. To do these experiments, the commercial polyacrylonitrile (PAN) fiber of Polyacryl Iran Corporation (PIC) was used as the precursors. The results show that increasing all of parameters improves tensile strength performance. ANFIS was applied to predict tensile strength of carbon fibers as a function of stabilization temperature at first stage (STFIS), stabilization temperature at second stage (STSS), stabilization temperature at third stage (STTS), stabilization temperature at fourth stage (STFOS), and carbonization temperature (CT). The optimum levels of influential factors, determined for tensile strength are STFIS 200 °C, STSS 225 °C, STTS 240 °C, STFOS 260 °C, CT, and 1400 °C. The modeling results showed that there is an excellent agreement between the experimental data and the predicted values. Furthermore, the fiber process is optimized applying differential evolution (DE) algorithm as an effective and robust optimization method.     

Synthesis and characterization of boron doped alumina stabilized zirconia fibers

Boron doped PVA/Zr-Al acetate nanofibers were prepared by electrospinning using PVA as a precursor. The effect of calcination temperature on morphology and crystal structure was investigated at 250, 500, and 800 °C. The study also establishes the effect of boron doping on the morphology of PVA/Zr-Al acetate nanofibers at various calcination temperatures. The measurements showed that the conductivity, pH, viscosity and the surface tension of the hybrid polymer solutions have increased with boron doping. In addition, the fibers were characterized by FTIR, DSC, XPS, XRD and SEM techniques. The addition of boron did not only increase the thermal stability of the fibers, but also increased the average fiber diameters, which gave stronger fibers. The DSC results indicated that the melting temperature (Tm) of the fibers was increased from 256 to 270 °C with the addition of boron. XRD peak patterns showed that after further heat treatment at 800 °C, zirconia exists in two phases of tetragonal and monoclinic modifications. Moreover, alumina does not transform into the γ-Al₂O₃ and θ-Al₂O₃ phase at 800 °C. The SEM appearance of the fibers showed that the addition of boron resulted in the formation of crosslinked bright surfaced fibers.     

Copolymerization of benzyl methacrylate and a methacrylate bearing benzophenoxy and hydroxyl side groups: Monomer reactivity ratios,thermal studies and dielectric measurements

Statistical copolymers of 2-hydroxy-3-benzophenoxy propyl methacrylate (HBPPMA) and benzyl methacrylate (BzMA) in different feed ratios were synthesized by free radical copolymerization method at 60 °C in presence of AIBN initiator. The compositions of copolymer were estimated from ¹H-NMR technique. The monomer reactivity ratios of HBPPMA and BzMA were calculated as r₁ (r_HBPPMA)=0.51±0.076 and r₂ (r_BzMA)=1.07±0.140 for Kelen-Tüdos method, and was estimated as r₁=0.37±0.0006 and r₂=0.64±0.0485 according to Fineman Ross equation. The average values estimated from the two methods showed that monomer reactivity ratio of benzyl methacrylate was a slightly high in comparison to HBPPMA. The copolymer system showed an azeotropic point, which is equal to M _BzMA =m _BzMA =0.43. DSC measurements showed that the T_g’s of poly(HBPPMA) and poly(BzMA) were 84 °C and 73 °C, respectively. The T_g in the copolymer system decreased with increase in benzyl methacrylate content. The decomposition temperature of poly(BzMA) and poly(HBPPMA) occurs in a single stage at about 207 °C and 260 °C, respectively. Those of HBPPMA-BzMA copolymer systems are between decomposition temperatures of two homopolymers. The dielectric constant, dielectric loss factor and electrical conductivity were investigated depend on the frequency of the copolymers. The highest dielectric constants depending on all the studied frequencies were recorded for the poly(HBPPMA) and the copolymer containing the highest HBPPMA unit. The dielectric constant for P(HBPPMA) and P(BzMA) at 1 kHz are 6.56 and 3.22, respectively. Also, those of copolymer systems were estimated between these two values. Similarly, poly(HBPPMA) and copolymers, which are prepared under the same conditions show the dissipation factor and conductivity as well.     

Preparation and properties of fibers produced from a cellulose/complex PA solvent system precipitating in diverse coagulants

Ethanol, as the first coagulation bath, and several common organic solvents, as well as aqueous solutions of NH₄Cl, NaHCO₃ and NaOH were explored and demonstrated to be adopted as the second coagulation bath for cellulose/phosphoric acid/tetraphosphoric acid (cellulose/complex PA solvent) solution to produce novel cellulose fibers by two-stage dry-wet spinning in a laboratory scale, and effect of coagulants, cellulose concentration, solvent concentration (P₂O₅ concentration) and coagulation temperature on crystal structure and properties of corresponding fibers were investigated. Surface morphology of regenerated fibers as-spun from different coagulants was observed by scanning electronic microscope (SEM), indicating that methanol and 8 wt% NaOH aqueous solution all rendered cellulose fibers relatively dense and smooth surface. X-ray diffraction (XRD) analysis showed that cellulose fiber precipitated from 8 wt% NaOH aqueous solution had pronounced characteristic peak of cellulose II than those of fibers precipitated from other coagulants, and highest crystallinity and orientation. Meanwhile, those two coagulants referred above also gave cellulose fibers relatively higher tensile strength under the same prerequisite. TGA curves exhibited that fibers were thermally stable produced from two salt aqueous solutions (8 wt% NH₄Cl and NaHCO₃) since they had the relatively higher onset decomposition temperatures. By evaluating the effect of cellulose concentration, P₂O₅ concentration and coagulation temperature on the structure and properties of asprepared fibers, it was preferable to produce cellulose fiber from a solution at 20 wt% cellulose concentration, 73 % P₂O₅ concentration, and coagulating in methanol at coagulation temperature of 60 °C at the second-stage.     

High performance fibers production process using Taguchi experimental design

In this research, results of an experimental interaction effect of operating parameters on tensile strength carbon fibers from a commercial PAN-based precursor are investigated. Ten parameters at two and four levels (L₃₂=2¹×4⁹) were investigated: stabilization temperature at first stage (STFIS), stabilization duration time at first stage (SDTFIS), stabilization temperature at second stage (STSS), stabilization duration time at second stage (SDTSS), stabilization temperature at third stage (STTS), stabilization duration time at third stage (SDTTS), stabilization temperature at fourth stage (STFOS), stabilization duration time at fourth stage (SDTFOS), carbonization temperature (CT), and carbonization duration time (CDT). In this study, Taguchi method was used initially to plan a minimum number of experiments. Statistical analysis, analysis of variance (ANOVA), was also employed to determine the relationship between experimental conditions and yield levels. ANOVA was applied to calculate sum of square, variance, ratio of factor variance to error variance and contribution percentage of each factor on response. The results show that increasing all of parameters improves tensile strength performance. The optimum levels of influential factors, determined for tensile strength are STFIS 200 °C, SDTFIS 120 min, STSS 225 °C, SDTSS 120 min, STTS 240 °C, SDTTS 120 min, STFOS 260 °C, SDTFOS 60 min, CT 1400 °C and CDT 10 min. The results showed that CT and ODTFIS are the most and the less effective factors on response, respectively.     

Heat resistance,impact strength,and transparency of PET copolymer containing fluorenylidene bis(2-phenoxyethanol)

Poly(ethylene terephthalate) (PET) copolymers containing fluorenylidene bis(2-phenoxyethanol) (FBPE) were prepared. The glass transition temperature of copolymers increased continuously with the composition of FBPE. The glass transition temperature of PET/FBPE copolymer at loading of 15 mol% FBPE was 107 °C, which was 35 °C higher than that of PET. The melting temperature of PET/FBPE copolymers was decreased with the composition of FBPE, and it disappeared above 6 mol% of FBPE. The heat deflection temperature of copolymers increased from 60.7 °C for PET to 89.9 °C for the copolymer containing 15 mol% of FBPE. The values of optical transmittance of copolymers were 89-90 % at 550 nm, and no significant change was observed with the FBPE composition. The impact strength value of copolymer at loading of 10 mol% FBPE was 26 J/m, which was 20 J/m higher than that of PET.     

Impact of biodiversity-climate futures on primary production and metabolism in a model benthic estuarine system

Background  

Understanding the effects of anthropogenically-driven changes in global temperature, atmospheric carbon dioxide and biodiversity on the functionality of marine ecosystems is crucial for predicting and managing the associated impacts. Coastal ecosystems are important sources of carbon (primary production) to shelf waters and play a vital role in global nutrient cycling. These systems are especially vulnerable to the effects of human activities and will be the first areas impacted by rising sea levels. Within these coastal ecosystems, microalgal assemblages (microphytobenthos: MPB) are vital for autochthonous carbon fixation. The level of in situ production by MPB mediates the net carbon cycling of transitional ecosystems between net heterotrophic or autotrophic metabolism. In this study, we examine the interactive effects of elevated atmospheric CO₂ concentrations (370, 600, and 1000 ppmv), temperature (6°C, 12°C, and 18°C) and invertebrate biodiversity on MPB biomass in experimental systems. We assembled communities of three common grazing invertebrates (Hydrobia ulvae, Corophium volutator and Hediste diversicolor) in monoculture and in all possible multispecies combinations. This experimental design specifically addresses interactions between the selected climate change variables and any ecological consequences caused by changes in species composition or richness.     

Investigation of the high-amylose maize starch gelatinization behaviours in glycerol-water systems

The effect of glycerol on gelatinization behaviours of high-amylose maize starch was evaluated by confocal laser scanning microscopy (CLSM), scanning electronic microscope (SEM), differential scanning calorimetry (DSC), texture analyzer (TPA) and rheometer. Gelatinization of the high-amylose maize starches with glycerol content of 10% (w/w) began at 95.4 °C (T_o), peaked at 110.3 °C (T_p), and completed at 118.9 °C (T_c). The birefringence began to disappear at around 100 °C and finished at 120 °C which corresponded well to the onset and conclusion temperatures obtained by DSC. The high-amylose maize starch granules maintained original morphological structure at 100 °C and swelled to a great degree at 110 °C. The high-amylose maize starch paste formed at 100 °C showed the lowest hardness (39.92 g), while at 120 and 130 °C, showed the highest hardness (610.89 g and 635.43 g, respectively). It should be noted that in going from 100 °C to 110 °C there is a significant increase in the viscosity of the slurry solution. The identical apparent viscosity was observed when the shear rate exceed 100 s⁻¹, resulting from the high-amylose maize starch granules were completely gelatinized at 120 °C, which was consistent with DSC analysis.     

Thermal degradation behaviors and fire retardant properties of poly(1,3,4-oxadiazole)s (POD) and poly(m-phenylene isophthalamide) (PMIA) fibers

Thermal degradation behaviors and fire retardant properties of poly(1,3,4-oxadiazole)s (POD) and poly(m-phenylene isophthalamide) (PMIA) fibers were investigated. The thermal gravimetric analysis (TGA) demonstrated that POD exhibited higher onset thermal degradation temperature (T_onset) than PMIA, exceeding nearly 80 °C. The thermal degradation kinetics, evaluated by the modified Coats-Redfern method, displayed that the apparent activation energy (E_a) of POD and PMIA fibers was similar when the conversion rate (α) ranges from 0.2 to 0.5, while with the α from 0.6 to 0.8, the E_a of POD was significantly lower than that of PMIA. The fire retardant performance of POD and PMIA fibers were evaluated by cone calorimeter under heat fluxes of 35, 50 and 75 kW/m², during which the temperature of the fibers were monitored by a thermocouple. Surprisingly, POD fibers showed inferior fire retardant performance in comparison with PMIA, with lower time to ignition (TTI) and higher peak heat release rate (PHRR). The origin of the different fire retardant properties of both fibers was revealed by analyzing the residual chars and gaseous products during thermal pyrolysis. The morphology confirmed that stable and compact chars can be formed in PMIA. In addition, the Fourier Transform Infrared Spectroscopy (FTIR) characterization of the residual char revealed that POD can form carbonaceous chars at the heat flux of 50 kW/m², while the heat flux of PMIA was 75 kW/m². The pyrolysis products characterized by pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS) indicated that POD can be pyrolyzed completely at 600 °C, while the temperature of PMIA was 700 °C.     

TEMPO-mediated oxidation of MCC at high temperature: Synthesis and characterization of high-hydrophilic polymer

Microcrystalline cellulose was reacted with catalytic amounts of 2, 2, 6, 6-tetramethyl-1-piperidine oxoammonium salt (TEMPO), sodium hypochlorite and sodium bromide in Na₂CO₃/NaHCO₃ buffer solution at different temperatures (30 °C, 40 °C, 50 °C). The oxidation procedures included first oxidation and second oxidation. The yield of cellouronic acid produced in the second oxidation was higher than the yield of cellouronic acid produced in the first oxidation at the same oxidation temperature. Moreover, an interesting “high-hydrophilic” phenomenon appeared at higher temperature during microcrystalline cellulose second oxidation (30 °C, 40 °C, 50 °C). Properties associated with the chemical characteristics are discussed by XRD, FTIR, ¹³C-NMR and Laser Particle Analyzer in view of its interesting high-hydrophilic effects.     

Spinnability in pre-gelled gel spinning of polyacrylonitrile precursor fibers

The spinnability in pre-gelled gel spinning of polyacrylonitrile (PAN) precursor fibers was investigated. The spinning solutions were aged at 25 °C for different times prior to fiber spinning. The pre-gelled spinning solution aged for 2.5 h was much more strain hardening than the ungelled one, which can increase the spinnability of the solution. The maximum take-up velocity of the first winding roller V _1m, which reflects the spinnability of the spinning solutions, was found to be largest when the aging time was 1.5 h. The spinnability increased with the increase of the air gap length and the lengthdiameter ratio L/D of the spinnerette. Once the L/D increased beyond 15, the spinnability hardly changed. The fibers spun from the spinning solution aged for 1.5 h had the best mechanical properties and favorable structure, showing that good spinnability favors the performance increase of resultant PAN precursor fibers.     

Synthesis of high performance phosphorine antioxidants and their application to mCOC

Cyclic olefin copolymers, mCOC, produced using a metallocene catalyst, have been developed since 1990. Besides their high cost and difficulty of processing, oxidation and degradation are one of the critical problems in commercializing high-T_g mCOC products. In this work, a series of mCOCs whose T_g values were 132 °C, 194 °C and 260 °C were synthesized successfully. Additionally, high-performance phosphorine antioxidants, 1,4-di[6-oxo-dibenz[c,e][1,2] oxaphosphorine] benzene (HPB) and 2,5-di-tert-butyl-1,4-di[6-oxo-dibenz[c,e][1,2] oxaphosphorine]benzene(HTPB) were synthesized. The oxidation induction time (OIT), the carbonyl index (CI) and the yellowness index (YI) were determined by DSC, FTIR and spectrophotometry, respectively. The results indicate that blending phosphorine antioxidants with hindered phenolic antioxidant, increases the OIT from 31.8 to 44.1 mins and causes the synergy to exceed 180 %. The CI variation showed that the embrittlement time could be increased from 100 hrs to over 450 hrs by thermal aging at 140 °C. Finally, the YI dropped from 29.3 to 9.2. Briefly, HTPB and HPB, successfully synthesized herein, exhibit a synergy with hindered phenolic agents in antioxidant performance for mCOC polymer.     

Study of microstructure of oriented PET fibres exposed to supercritical carbon dioxide

Samples of partially oriented yarn (POY) PET fibers were uniaxially drawn at temperatures below, near, and above the glass transition temperature at a constant draw ratio before exposure to supercritical carbon dioxide (scCO₂) in the presence of tension at a temperature of 80 °C and a pressure of 220 bar. The effects of drawing temperature and scCO₂ exposure on structural changes and on mesomorphic transitions, in particular, were investigated using differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and birefringence and density measurements. A good correlation was obtained among the results obtained from various techniques. Results indicated that the development of a transient mesophase structure depended strongly on process temperature. By drawing PET fibers in the samples at temperatures below the glass transition (cold-drawing), a mesophase structure developed in which the highly extended chains played a key role in structural changes incurred. Meanwhile, exposure to scCO₂ led to the plasticization of the samples accompanied by their reduced glass transition and cold crystallization temperatures. This process also gave rise to the appearance of a second melting peak at about 135 °C that is related to the melting of imperfect and thin crystals, thereby inducing structural changes in the treated fibers. In the case of samples subjected to cold drawing and to scCO₂ exposure, the transformation of the mesophase structure into the crystalline phase was found to be strongly affected by scCO₂ exposure, while this same effect was negligible in the case of hot drawn samples.     

Evaluation of the In vitro Anti-hyperglycemic Effect of Cinnamomum cassia Derived Phenolic Phytochemicals,via Carbohydrate Hydrolyzing Enzyme Inhibition

Cinnamomum cassia (cinnamon) proanthocyanidins (PACs) are believed to have anti-hyperglycemic potential via stimulation of insulin sensitivity. The present study investigates the carbohydrate hydrolyzing enzyme inhibition of cinnamon PACs. Five grams of cinnamon bark powder were extracted in 100 mL acetone solution (CAE) (acetone: water: hydrochloric acid, 70:29.9:0.01) for 2 h at room temperature and in 100 mL deionized water for 30 min at 90 °C (CWE). PACs were purified from CAE using LH-20 (CAE-PAC) to be further evaluated. PAC contents were evaluated by 4-Dimethylaminocinnamaldehyde (DMAC) assay and yielded 795, 177 and 123 mg/g, for CAE-PAC, CAE and CWE respectively. The total phenolic contents of CAE and CWE were determined to be 152 and 134 mg/g respectively. All extracts were adjusted to the same PAC content (180, 90, 45 and 20 μg) and the inhibitory activity against rat α-glucosidase was determined. The CAE-PAC fraction had very low rat α-glucosidase inhibitory activity, CAE had the highest (IC₅₀ 0.474 mg/mL total phenolic (TP) basis) followed by CWE (IC₅₀ 0.697 mg/mL TP basis). The specific maltase and sucrase inhibitory activities were determined and CAE (IC₅₀ 0.38 and 0.10 mg/mL TP basis) had higher inhibition than CWE (IC₅₀ 0.74 and 0.37 mg/mL TP basis). Results suggest that the observed bioactivity is not PAC dependent and that CAE has a higher anti-hyperglycemic potential than CWE via inhibition of carbohydrate hydrolyzing enzymes.     

Preparation of regenerated cellulose fiber via carbonation. I. Carbonation and dissolution in an aqueous NaOH solution

Cellulose carbonate was prepared by the reaction of cellulose pulp and CO₂ with treatment reagents, such as aqueous ZnCl₂ (20–40 wt%) solution, acetone or ethyl acetate, at −5–0°C and 30–40 bar (CO₂) for 2 hr. Among the treatment reagents, ethyl acetate was the most effective. Cellulose carbonate was dissolved in 10% sodium hydroxide solution containing zinc oxide up to 3 wt% at −5–0°C. Intrinsic viscosities of raw cellulose and cellulose carbonate were measured with an Ubbelohde viscometer using 0.5 M cupriethylenediamine hydroxide (cuen) as a solvent at 20°C according to ASTM D1795 method. The molecular weight of cellulose was rarely changed by carbonation. Solubility of cellulose carbonate was tested by optical microscopic observation, UV absorbance and viscosity measurement. Phase diagram of cellulose carbonate was obtained by combining the results of solubility evaluation. Maximum concentration of cellulose carbonate for soluble zone was increased with increasing zinc oxide content. Cellulose carbonate solution in good soluble zone was transparent and showed the lowest absorbance and the highest viscosity. The cellulose carbonate and its solution were stable in refrigerator (−5°C and atmospheric pressure).     

TEMPO-mediated oxidation of microcrystalline cellulose: Influence of temperature and oxidation procedure on yields of water-soluble products and crystal structures of water-insoluble residues

A series of microcrystalline cellulose samples were reacted with catalytic amounts of 2, 2, 6, 6-tetramethyl-1-piperidine oxoammonium salt (TEMPO), sodium hypochlorite and sodium bromide in Na₂CO₃/NaHCO₃ buffer solution at different temperature (15 °C, 20 °C, 30 °C, 35 °C, 40 °C, 50 °C). The oxidation procedures included first and second oxidation. The first oxidation was a classical process for activating cellulose for the second oxidation. A substantial increase in the reactivity of the second oxidation cellulose samples was observed in comparison to those in the first oxidation and a relationship between oxidation procedures and accessibility of cellulose primary hydroxyl groups was directly established. For the characterization, we have used several methods, mainly XRD, FTIR. In all samples, the partial primary alcohol groups were selectively oxidized into carboxyl groups. The reaction during the first oxidation procedure mainly occurs in disordered regions of MCC and crystal surface. But the second oxidation procedure took place not only in disordered regions and crystal surface but inside crystalline region of cellulose I.     

Vacuum Drying for Extending Litchi Shelf-Life: Vitamin C,Total Phenolics,Texture and Shelf-Life Assessment

In an attempt to obtain shelf-stable litchi fruit with preserved nutritional quality and good sensory features, quarters of peeled and pitted fruits were vacuum dried at 50, 60 and 70 °C at a constant pressure of 8.0 kPa. The product was assessed for its vitamin C, total phenolics and texture (hardness). In addition, the product with the best texture was assessed for its shelf-life by means of accelerated testing. Results suggest that vacuum dried litchi retained almost 70% of the vitamin C and total phenolics when compared to frozen fruits (control). Vitamin C and phenolic compounds content significantly decreased with drying, while no difference was found between different drying temperatures. Hardness increased with drying temperature. The sample dried at 70 °C presented crispness, which is a desired quality feature in dried fruit products. This sample was subjected to shelf-life evaluation, whose result suggests a shelf-life of eight months at 23 °C. Total color change (CIE ΔE₀₀) was the expiry criterion. Vacuum drying was a suitable technique for producing shelf-stable litchi fruit with good texture while preserving its desirable original nutrients. Consumption of vacuum dried litchi may be beneficial to health due to its remarkable content of phenolic compounds and vitamin C.