scholarly journals Enhancing the Dyeability of Polypropylene Fibers by Melt Blending with Polyethylene Terephthalate

2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Fereshteh Mirjalili ◽  
Siamak Moradian ◽  
Farhad Ameri
Keyword(s):  
Polyethylene Terephthalate ◽  
Tensile Testing ◽  
Disperse Dyes ◽  
Polypropylene Fibers ◽  
Melt Blending ◽  
Thermal And Mechanical Properties ◽  
Scanning Calorimetry ◽  
Dyeing Performance ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Attempts were made to modify polypropylene fibers by melt blending with polyethylene terephthalate in order to enhance the dyeability of the resultant fiber. Five blends of polypropylene/polyethylene terephthalate/compatibilizer were prepared and subsequently spun into fibers. Three disperse dyes were used to dye such modified fibers at boiling and 130°C. The dyeing performance of the blend fibers, as well as the morphological, chemical, thermal, and mechanical properties, of the corresponding blends was characterized by means of spectrophotometry, polarized optical microscopy, scanning electron microscopy (SEM), FT-IR spectroscopy, differential scanning calorimetry (DSC), and tensile testing.

GROWTH AND STUDIES OF PROPERTIES OF COPPER SUCCINATE DIHYDRATE SINGLE CRYSTALS

2013 ◽  
Vol 27 (11) ◽  
pp. 1350073
Author(s):  
M. P. BINITHA ◽  
P. P. PRADYUMNAN
Keyword(s):  
Differential Scanning Calorimetry ◽  
Dielectric Constant ◽  
Single Crystals ◽  
Scanning Calorimetry ◽  
Force Microscopy ◽  
Atomic Force ◽  
Different Temperatures ◽  
Triclinic Structure ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Single crystals of copper succinate dihydrate (CSD) with triclinic structure were grown in silica gel medium. The functional groups in the crystal were analyzed by FT-IR Spectroscopy. Atomic Force Microscopy (AFM) revealed the striations on the surface of grown crystals, which were incorporated during its time of growth. Thermal degradation studies have been carried out by Differential Scanning Calorimetry (DSC). Dielectric constant and AC conductivity have been estimated as a function of frequency at different temperatures.

COLORATION OF POLYETHYLENE TEREPHTHALATE (PET) FILM BY 3MeV PROTON BEAMS

2001 ◽  
Vol 11 (03n04) ◽  
pp. 93-101 ◽  
Author(s):  
S. Matsuyama ◽  
K. Ishii ◽  
H. Yamazaki ◽  
H. Endoh ◽  
H. Yuki ◽  
...  
Keyword(s):  
Polyethylene Terephthalate ◽  
Color Centers ◽  
Sequential Process ◽  
Proton Beams ◽  
Spin Resonance ◽  
Ft Ir ◽  
Absorbance Changes ◽  
Pet Film ◽  
Pet Films ◽  
Ft Ir Spectroscopy

Coloration of polyethylene terephthalate (PET) films by using 3 MeV proton beams was studied by means of absorption spectroscopy, electron spin resonance (ESR) spectroscopy and Fourier transform infrared absorption (FT-IR) spectroscopy. Absorbance of the films increased with the dose and faded in time. Absorbance changes are caused by formation of color centers. The color centers had three components: permanent, long-lived and short-lived. Long-lived and short-lived color centers were formed by reactive species such as radicals. Annealing of color center is well explained by a proposed sequential process.

scholarly journals Characterization of the Spindle Morphology Nanomicelles Assembled from Sericin and Gelatin

2017 ◽  
Vol 2017 ◽  
pp. 1-9
Author(s):  
Xiaozhou Su ◽  
Lei Li ◽  
Weihan Huang
Keyword(s):  
Electron Microscopy ◽  
Protein Concentration ◽  
Scanning Calorimetry ◽  
Force Microscopy ◽  
Atomic Force ◽  
Transmission Electron ◽  
Ft Ir ◽  
And Storage ◽  
Ft Ir Spectroscopy

Complex nanomicelles were prepared by sericin and type A gelatin with molecular weight of 5789 Da and 128664 Da separately. The assembling conditions were as follows: mass ratio (sericin/gelatin) was 1 : 1, protein concentration was 0.5%, temperature was 35°C, and assembling time was 18 hours. Scanning electron microscopy (SEM), atomic force microscopy (AFM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), and dynamic light scattering (DLS) were conducted to observe and characterize the complex nanomicelles. Results showed that the complex sericin/gelatin micelles was a kind of nanospindle micelles. The micelles had high electrochemical stability, thermal stability, antidilution stability, and storage stability.

scholarly journals Influence of Chain-Extension Reaction on Stereocomplexation, Mechanical Properties and Heat Resistance of Compressed Stereocomplex-Polylactide Bioplastic Films

Polymers ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1218 ◽  
Author(s):  
Yodthong Baimark ◽  
Sumet Kittipoom
Keyword(s):  
Mechanical Properties ◽  
Differential Scanning Calorimetry ◽  
Heat Resistance ◽  
Tensile Testing ◽  
Chain Extender ◽  
Chain Extension ◽  
Melt Blending ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Xrd Patterns

Stereocomplex polylactide (scPLA) films were prepared by melt blending of poly(l-lactide) (PLLA) and poly(d-lactide) (PDLA) with and without an epoxy-based chain extender before compression molding. The obtained scPLA films were characterized through differential scanning calorimetry, X-ray diffractometry (XRD), tensile testing and dimensional stability to heat. XRD patterns revealed that all the scPLA films had only stereocomplex crystallites. The obtained results showed that the chain-extension reaction improved mechanical properties of the scPLA films, however, it suppressed stereocomplexation and heat resistance.

scholarly journals Inclusion of the Phytoalexin trans-Resveratrol in Native Cyclodextrins: A Thermal, Spectroscopic, and X-Ray Structural Study

Molecules ◽  
2020 ◽  
Vol 25 (4) ◽  
pp. 998 ◽  
Author(s):  
Laura Catenacci ◽  
Milena Sorrenti ◽  
Maria Cristina Bonferoni ◽  
Lee Hunt ◽  
Mino R. Caira
Keyword(s):  
Inclusion Complexation ◽  
Exothermic Effect ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Physical Mixing ◽  
Ft Ir ◽  
Co Precipitation ◽  
Ft Ir Spectroscopy ◽  
Severe Disorder

The aim of the study was to determine the feasibility of complexation between the antioxidant trans-resveratrol (RSV) and underivatized cyclodextrins (CDs) using a variety of preparative methods, including physical mixing, kneading, microwave irradiation, co-evaporation, and co-precipitation techniques. Products were characterized using differential scanning calorimetry (DSC), simultaneous thermogravimetric/DSC analysis (TGA/DSC), Fourier transform infrared (FT-IR) spectroscopy, and powder X-ray diffraction (PXRD). With α-CD and RSV, sample amorphization was revealed by PXRD and FT-IR, but no definitive inclusion complexation was evident. Similar results were obtained in attempts to complex RSV with β-CD. However, complex formation between γ-CD and RSV was evident from observation of an endo-/exothermic effect appearing in the DSC trace of the product from kneading and was further corroborated by FT-IR and PXRD methods. The latter technique indicated complexation unequivocally as the diffraction peak profile for the product matched that for known isostructural γ-CD complexes. Single crystal X-ray analysis followed, confirming the predicted complex between γ-CD and RSV. A combination of 1H NMR and TGA data yielded the complex formula (γ-CD)3·(RSV)4·(H2O)62. However, severe disorder of the RSV molecules prevented their modeling. In contrast, our previous studies of the inclusion of RSV in methylated CDs yielded crystals with only minor guest disorder.

scholarly journals The plasticizing effect of properties of manganous chloride and glycerin on poly(vinyl alcohol)

2015 ◽  
Vol 17 (2) ◽  
pp. 29-33
Author(s):  
Puyou Jia ◽  
Meng Zhang ◽  
Caiying Bo ◽  
Lihong Hu ◽  
Yonghong Zhou
Keyword(s):  
Vinyl Alcohol ◽  
Poly Vinyl Alcohol ◽  
Thermal And Mechanical Properties ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Elongation At Break ◽  
X Ray ◽  
Ft Ir ◽  
Micro Morphology ◽  
Lower Tensile Strength

Abstract Poly(vinyl alcohol) films were prepared with manganous chloride (MnCl2 · 4H2O) and glycerin as complex plasticizer. The micro morphology of pure PVA film and complex plasticizer plasticized PVA films was observed by scanning electron microscope (SEM). The interaction between complex plasticizer and PVA molecules was investigated by Fourier transform infrared spectroscopy (FT-IR). The influence of complex plasticizer on crystalline, thermal and mechanical properties of PVA films was studied by X-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TG), and tensile testing, respectively. The results showed that the complex plasticizer of MnCl2 · 4H2O/glycerin could interacted with PVA molecular and then effectively destroy the crystals of PVA. PVA films plasticized with complex plasticizer of MnCl2 · 4H2O/glycerin became soft and ductile, with lower tensile strength and higher elongation at break compared with PVA films. This is an important cause of plasticization of the complex plasticizer of MnCl2 · 4H2O/glycerin on PVA films.

Synthesis and Characterization of Triethanolamine Borate

2013 ◽  
Vol 709 ◽  
pp. 28-31
Author(s):  
Cheng Xue Wang ◽  
Tian Tian Liang ◽  
Chun Qiao Wei
Keyword(s):  
Mass Spectrometry ◽  
Differential Scanning Calorimetry ◽  
Synthesis And Characterization ◽  
Spectroscopy Analysis ◽  
Scanning Calorimetry ◽  
Reaction Conditions ◽  
Different Types ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Starting with boric acid and triethanolamine , the effect of the different types of the water-carrying agent on the yield was invested, and influences of dosage of water-carrying agent ,the mole ratio of reactants, reaction time on yield were discussed, the optimized reaction conditions were confirmed. The structure of the product was described by Fourier transform-infrared (FT-IR) spectroscopy, NMR Spectroscopy analysis, mass spectrometry (MS) and thermodynamic properties was analyzed by differential scanning calorimetry (DSC) and thermogravimetry (TG).

scholarly journals THE STUDY OF THERMAL IMPACT ON THE TRANSFORMATION OF ASPEN WOOD AND BARK

2017 ◽  
pp. 53-64 ◽  
Author(s):  
Надежда (Nadezhda) Михайловна (Mikhailovna)) Микова(Mikova) ◽  
Ольга (Ol'ga) Юрьевна (Yur'evna) Фетисова (Fetisova) ◽  
Иван (Ivan) Петрович (Petrovich) Иванов (Ivanov) ◽  
Нина (Nina) Ивановна (Ivanovna) Павленко (Pavlenko) ◽  
Николай (Nikolaj) Васильевич (Vasil'evich) Чесноков (Chesnokov)
Keyword(s):  
Thermal Decomposition ◽  
Thermal Destruction ◽  
Scanning Calorimetry ◽  
Temperature Range ◽  
Air Atmosphere ◽  
Adsorption Of Nitrogen ◽  
Ft Ir ◽  
Loss Of Mass ◽  
Two Temperature ◽  
Ft Ir Spectroscopy

Thermal gravimetry analysis (TGA) and differential scanning calorimetry (DSC), scanning electron microscopy (SEM), FT-IR spectroscopy, and thermal adsorption of nitrogen (BET) methods were used to study the thermal destruction of woody biomass of aspen (bark and wood) in argon and air in the temperature range from 25 to 800 °C. The composition and properties of the products obtained as a result of thermal decomposition of the initial wood biopolymers are characterized. It is established that the main range of thermal decomposition of wood in an inert medium included an interval from 227 to 500 °C, and aspen bark covered a temperature range from 180 to 600 °C. In the air atmosphere, the temperature zone of thermal decomposition narrows, the loss of mass of matter is observed in two temperature intervals of preferential decomposition of the substance with a shift toward a decrease in the maximum rate of decomposition for the bark (~40 °C), and for wood – 34,6 °C.

scholarly journals Swelling Behaviour of Starch-g-Acrylic Acid Hydrogel and its Potential Application in Removal of Rhodamine B and Alkali Blue Dyes

2021 ◽  
Vol 18 (2) ◽  
pp. 98-104
Author(s):  
S. Yahaya ◽  
Z.I.S.G. Adiya ◽  
S. S. Adamu ◽  
H.B. Bature ◽  
I.B. Ibrahim
Keyword(s):  
Ir Spectroscopy ◽  
Acrylic Acid ◽  
Rhodamine B ◽  
Dye Adsorption ◽  
Batch Adsorption ◽  
Scanning Calorimetry ◽  
Adsorption Method ◽  
Ft Ir ◽  
Percentage Removal ◽  
Ft Ir Spectroscopy

Starch-g-acrylic acid hydrogel was prepared by free radical polymerization technique adopting potassium persulphate (KPS) as an initiator and N’N-methylenebisacrylamide (MBA) as a linking agent. The aim of the research is to inspect the potentials of starch-based hydrogel in remediating wastewater. Fourier Transform Infrared (FT-IR) spectroscopy was used to find the formation of hydrogel while Differential Scanning Calorimetry (DSC) and Scanning Electron Microscopy (SEM) were used for the characterization of the hydrogel. The FT-IR spectroscopy confirmed hydrogel formation. The DSC results showed that the generated hydrogel is thermally stable, and the SEM depicts a good porous site for dye adsorption. Batch adsorption for Rhodamine B (RDB) and Alkali blue (AB) dyes under the variation of contact time was 105 minutes for both dyes with percentage removal of 89.80 and 60.32%, adsorbent dose was 0.4 and 0.8 g with percentage removal of 86.42 and 57.95%, concentration was 50 and 30 ppm with percentage removal of 67.01 and 77.18% and pH was 8 for both dyes with percentage removal of 77.43 and 79.13% as the optimum. The results indicates that acrylic acid monomer was efficiently grafted on the starch, and the adsorption method correlated with Freundlich isotherm equation. It was concluded that the starch-based hydrogel is an appropriate adsorbent and can be explored for industrial wastewater treatment.

Mechanochemical synthesis insights and solid-state characterization of quininium aspirinate, a glass-forming drug–drug salt

2021 ◽  
Vol 77 (9) ◽  
Author(s):  
Nehemiah Harris ◽  
Jubilee Benedict ◽  
Diane A. Dickie ◽  
Silvina Pagola
Keyword(s):  
Crystal Structure ◽  
Differential Scanning Calorimetry ◽  
Ir Spectroscopy ◽  
Mechanochemical Synthesis ◽  
Mechanochemical Reaction ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Quinine (an antimalarial) and aspirin (a nonsteroidal anti-inflammatory drug) were combined into a new drug–drug salt, quininium aspirinate, C20H25N2O2 +·C9H7O4 −, by liquid-assisted grinding using stoichiometric amounts of the reactants in a 1:1 molar ratio, and water, EtOH, toluene, or heptane as additives. A tetrahydrofuran (THF) solution of the mechanochemical product prepared using EtOH as additive led to a single crystal of the same material obtained by mechanochemistry, which was used for crystal structure determination at 100 K. Powder X-ray diffraction ruled out crystallographic phase transitions in the 100–295 K interval. Neat mechanical treatment (in a mortar and pestle, or in a ball mill at 20 or 30 Hz milling frequencies) gave rise to an amorphous phase, as shown by powder X-ray diffraction; however, FT–IR spectroscopy unambiguously indicates that a mechanochemical reaction has occurred. Neat milling the reactants at 10 and 15 Hz led to incomplete reactions. Thermogravimetry and differential scanning calorimetry indicate that the amorphous and crystalline mechanochemical products form glasses/supercooled liquids before melting, and do not recrystallize upon cooling. However, the amorphous material obtained by neat grinding crystallizes upon storage into the salt reported. The mechanochemical synthesis, crystal structure analysis, Hirshfeld surfaces, powder X-ray diffraction, thermogravimetry, differential scanning calorimetry, FT–IR spectroscopy, and aqueous solubility of quininium aspirinate are herein reported.

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