Polylactic acid flame-retarded by nano-compound of form II ammonium polyphosphate with montmorillonite

2021 ◽  
pp. 073490412110254
Author(s):  
Yinglin Liu ◽  
Yina Liu ◽  
Rongjie Yang
Keyword(s):  
Polylactic Acid ◽  
Large Scale ◽  
Oxygen Index ◽  
Crystal Form ◽  
Ammonium Polyphosphate ◽  
X Ray Diffraction ◽  
Limited Oxygen Index ◽  
X Ray ◽  
Flame Retarded ◽  
Limited Oxygen

It is reported a convenient method to obtain flame-retardant polylactic acid composite by adding low amount of crystal form II ammonium polyphosphate (APP-II) or nano-compound of crystal form II ammonium polyphosphate with calcium-based montmorillonite. The structures and thermal properties of the crystal form II ammonium polyphosphate and crystal form II ammonium polyphosphate with calcium-based montmorillonite were characterized by X-ray diffraction, Fourier-transform infrared spectroscopy, and thermogravimetric analysis. Crystallography and morphologies of the polylactic acid and its composites with the crystal form II ammonium polyphosphate and crystal form II ammonium polyphosphate with calcium-based montmorillonite were measured through differential scanning calorimeter and scanning electron microscopy. In flame retardancy of the polylactic acid composites, the 5 wt% crystal form II ammonium polyphosphate could make the polylactic acid achieve the UL-94 vertical burning V-0 rating and limited oxygen index 27.3%. When using crystal form II ammonium polyphosphate with calcium-based montmorillonite in flame-retarding polylactic acid, only 3 wt% nano-compound can result in the same V-0 rating level and the limited oxygen index of 28.0%. Meanwhile, polylactic acid with crystal form II ammonium polyphosphate or crystal form II ammonium polyphosphate with calcium-based montmorillonite still keeps the good mechanical properties. The developed systems are environmentally friendly and highly effective flame retarding, which show a promising future in practical large-scale polylactic acid application.

The Effect of Uniaxial Stretching on the Crystallization Behaviors of Polylactic Acid Film

2011 ◽  
Vol 418-420 ◽  
pp. 625-628 ◽  
Author(s):  
Hui Li Xie ◽  
Kai Guo ◽  
Jin Zhou Chen ◽  
Wan Jie Wang ◽  
Ming Jun Niu ◽  
...  
Keyword(s):  
Polylactic Acid ◽  
Crystallization Behavior ◽  
Crystal Form ◽  
Stretch Ratio ◽  
Uniaxial Tensile ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Uniaxial Stretching ◽  
X Ray ◽  
Stretching Ratio

Abstract. The effect of uniaxial stretching of different stretching ratio at 80 °C, 90°C, 100°C, 110 °C and 120°C on the crystallization behavior of polylactic acid (PLA) film was investigated by using differential scanning calorimetry (DSC), wide-angle X-ray diffraction (XRD) and polarizing microscope (POM). The results showed that the crystallinity of PLA film was improved via uniaxial tensile orientation and increased with increasing stretch ratio, and the crystallinity of PLA film reached the maximum under the conditions of 90°C and stretching ratio 300%. Stretched PLA films show α crystal form. The spherulites deform to ellipsoids after stretching.

Flame Retardant Properties of Two Different Synthetic Process of Ammonium Polyphosphates

2013 ◽  
Vol 668 ◽  
pp. 53-56
Author(s):  
Gou Sheng Liu ◽  
Yue Long Liu
Keyword(s):  
Flame Retardant ◽  
Oxygen Index ◽  
Intumescent Flame Retardant ◽  
Ammonium Polyphosphate ◽  
Synthetic Process ◽  
Limited Oxygen Index ◽  
Decomposition Processes ◽  
Ul 94 ◽  
Flame Retardant Properties ◽  
Limited Oxygen

Ammonium polyphosphate (APP) produced by non-P2O5 process and traditional P2O5 process were used in the intumescent flame retardant (IFR) polypropylene (PP) composite (IFR-PP). The composite was tested by limited oxygen index (LOI) and UL-94. TGA and SEM were used to study the decomposition processes. Results showed that when the ratio of APP-II/ pentaerythritol/melamine is 3/1/1, the LOI value is 33.1, and all composite could reach UL-94 V0 rating. The results showed that APP by non-P2O5 process had similar IFR properties as APP of traditional P2O5 process

scholarly journals Born out of Fire and Ice: Polymorph Studies of the Antiviral Famciclovir

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 129
Author(s):  
Liana Vella-Zarb ◽  
Ulrich Baisch
Keyword(s):  
Variable Temperature ◽  
Chemical Properties ◽  
Crystal Form ◽  
X Ray Diffraction ◽  
Crystal Forms ◽  
X Ray ◽  
Physical Chemical ◽  
Diffraction Patterns ◽  
Crystalline Forms

There is much interest and focus on solid forms of famciclovir. However, in spite of the abundance of reported differences in oral bioavailability, compressibility, and other physical–chemical properties of the various crystal forms of this drug, very little precise structural analysis is available in the literature to date. The form used in the commercial formulation is the anhydrous form I. Patents and patent applications report three different anhydrous crystalline forms on the basis of unindexed powder diffraction patterns. Single-crystal and variable-temperature X-ray diffraction experiments using the commercially available anhydrous form of famciclovir were carried out and led not only to the crystal structure determination of the anhydrous form I, but also to discovery of a new crystal form of anhydrous famciclovir from powder data.

Structure and properties of polypropylene/organic rectorite nanocomposites

Clay Minerals ◽  
2009 ◽  
Vol 44 (1) ◽  
pp. 35-50 ◽  
Author(s):  
Yun Huang ◽  
Xiaoyan Ma ◽  
Guozheng Liang ◽  
Hongxia Yan
Keyword(s):  
Loss Modulus ◽  
Polarized Light ◽  
Clay Content ◽  
Crystal Form ◽  
Ammonium Bromide ◽  
Wide Angle ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Monoclinic Crystal ◽  
X Ray

AbstractMelt blending using a twin-screw extruder was used to prepare composites of polypropylene (PP)/organic rectorite (PR). The organic rectorite (OREC) was modified with dodecyl benzyl dimethyl ammonium bromide (1227). Wide-angle X-ray diffraction (WAXD) and transmission electron microscopy were used to investigate the dispersion of OREC in the composites. The d spacings of OREC in PR composites was greater than in OREC itself. The dispersion of OREC particles in the PP polymer matrix was fine and uniform when the clay content was small (2 wt.%). The rheology was characterized using a capillary rheometer. The processing behaviour of the PR system improved as the amount of OREC added increased. Non-isothermal crystallization kinetics were analysed using differential scanning calorimetry. It was shown that the addition of OREC had a heterogeneous nucleation effect on PP, and can accelerate the crystallization. However, only when fine dispersion was achieved, and at lower rates of temperature decrease, was the crystallinity greater. Wide-angle X-ray diffraction and polarized light microscopy were used to observe the crystalline form and crystallite size. The PP in the PR composites exhibited an a-monoclinic crystal form, as in pure PP, and in both cases a spherulite structure was observed. However, the smaller spherulite size in the PR systems indicated that addition of OREC can reduce the crystal size significantly, which might improve the ‘toughness’ of the PP. The mechanical properties (tensile and impact strength) improved when the amount of OREC added was appropriate. Dynamic mechanical analysis showed that the storage modulus (E′) and loss modulus (E″) of the nanocomposites were somewhat greater than those of pure PP when an appropriate amount of OREC was added. Finally, thermogravimetric analysis showed that the PR systems exhibited a greater thermal stability than was seen with pure PP.

Investigation of Residual Stress/Strain and Texture in a Large Dissimilar Metal Weld Using Synchrotron Radiation and Neutrons

2013 ◽  
Vol 772 ◽  
pp. 193-199 ◽  
Author(s):  
Carsten Ohms ◽  
Rene V. Martins
Keyword(s):  
Synchrotron Radiation ◽  
Neutron Diffraction ◽  
Residual Stresses ◽  
Large Scale ◽  
High Energy ◽  
X Ray Diffraction ◽  
Butt Weld ◽  
X Ray ◽  
Component Size ◽  
Thin Slice

Bi-metallic piping welds are frequently used in light water nuclear reactors to connect ferritic steel pressure vessel nozzles to austenitic stainless steel primary cooling piping systems. An important aspect for the integrity of such welds is the presence of residual stresses. Measurement of these residual stresses presents a considerable challenge because of the component size and because of the material heterogeneity in the weld regions. The specimen investigated here was a thin slice cut from a full-scale bi-metallic piping weld mock-up. A similar mock-up had previously been investigated by neutron diffraction within a European research project called ADIMEW. However, at that time, due to the wall thickness of the pipe, stress and spatial resolution of the measurements were severely restricted. One aim of the present investigations by high energy synchrotron radiation and neutrons used on this thin slice was to determine whether such measurements would render a valid representation of the axial strains and stresses in the uncut large-scale structure. The advantage of the small specimen was, apart from the easier manipulation, the fact that measurement times facilitated a high density of measurements across large parts of the test piece in a reasonable time. Furthermore, the recording of complete diffraction patterns within the accessible diffraction angle range by synchrotron X-ray diffraction permitted mapping the texture variations. The strain and stress results obtained are presented and compared for the neutron and synchrotron X-ray diffraction measurements. A strong variation of the texture pole orientations is observed in the weld regions which could be attributed to individual weld torch passes. The effect of specimen rocking on the scatter of the diffraction data in the butt weld region is assessed during the neutron diffraction measurements.

Preparation and Research on the Lateral Elastic Modulus of the MnO2 Nanowires

2013 ◽  
Vol 662 ◽  
pp. 84-87
Author(s):  
Yong Jiang ◽  
Jian Cheng Deng ◽  
Yan Huai Ding ◽  
Jiu Ren Yin ◽  
Ping Zhang
Keyword(s):  
Elastic Modulus ◽  
Crystal Form ◽  
Bending Test ◽  
X Ray Diffraction ◽  
Nanowire Diameter ◽  
X Ray ◽  
Three Point Bending ◽  
Force Microscopy ◽  
Atomic Force ◽  
Mno2 Nanowires

MnO2 nanowires with large aspect ratio were successfully synthesized via a hydrothermal method. In this method, Mn(NO3)2 was as a source of manganese and NH4NO3 as an oxidant. The structure and morphology of the MnO2 nanowires were characterized by X ray diffraction (XRD) and scanning electron microscope (SEM). Their lateral elastic modulus was characterized via a nanoscale three-point bending test by atomic force microscopy (AFM) equipped with picoforce. The results indicate that the crystal form of MnO2 was β-MnO2. The elastic modulus of the nanowires decreased with the increase in nanowire diameter. This elastic modulus was in the range of 33.36-77.84GPa as the diameter ranged from 240 to 185nm.

The Croonian Lecture, 1970 The structural basis of muscular contraction

1971 ◽  
Vol 178 (1051) ◽  
pp. 131-149 ◽  
Keyword(s):  
Large Scale ◽  
Muscular Contraction ◽  
Important Change ◽  
Structural Basis ◽  
X Ray Diffraction ◽  
New Era ◽  
X Ray ◽  
Biology I ◽  
The Times ◽  
Polypeptide Chains

A previous occasion on which the Croonian lecture was directly concerned with the mechanism of muscular contraction was in 1945, when it was delivered by Professor W. T. Astbury. On that occasion he commented that it was a sign of the times that a physicist should be asked to give the Croonian lecture, and went on to say, and I quote: ‘We are at the dawn of a new era, the era of “molecular biology”, as I like to call it, and there is an urgency about the need for more intensive application of physics and chemistry, and specially structural analysis, to biological problems.’ These were very prophetic words, and, as a physicist just entering biology, I was much interested to read them, and to learn about his experiments. The basic experimental finding which Astbury reported (1947) was that there did not seem to be any important change in the wide angle X-ray diagram from muscle upon contraction; hence it followed that muscles did not contract by any process which simply involved the large-scale disorientation of originally well-ordered polypeptide chains, nor by an alteration in chain configuration in the well-ordered parts of the structure. Astbury suggested instead that there might be ‘specifically active foci’ which one could perhaps paraphrase as ‘larger structural units’ (i.e. larger than individual polypeptide chains) concerned in contraction, which might be studied in the electron microscope or by low angle X-ray diffraction.

In-Situ Diffraction Studies of Gas Storage Materials on a Laboratory X-Ray System

2013 ◽  
Vol 1544 ◽  
Author(s):  
Marco Sommariva ◽  
Harald van Weeren ◽  
Olga Narygina ◽  
Jan-André Gertenbach ◽  
Christian Resch ◽  
...  
Keyword(s):  
Large Scale ◽  
Fossil Fuels ◽  
Reaction Chamber ◽  
Hydrogen Gas ◽  
Gas Pressure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Structural Modifications ◽  
Model Studies

ABSTRACTThe sorption processes for hydrogen and carbon dioxide are of considerable, and growing interest, particularly due to their relevance to a society that seeks to replace fossil fuels with a more sustainable energy source. X-ray diffraction allows a unique perspective for studying structural modifications and reaction mechanisms that occur when gas and solid interact. The fundamental challenge associated with such a study is that experiments are conducted while the solid sample is held under a gas pressure. To date in-situ high gas pressure studies of this nature have typically been undertaken at large-scale facilities such as synchrotrons or on dedicated laboratory instruments. Here we report high-pressure XRD studies carried out on a multi-purpose diffractometer. To demonstrate the suitability of the equipment, two model studies were carried out, firstly the reversible hydrogen cycling over LaNi5, and secondly the structural change that occurs during the decomposition of ammonia borane that results in the generation of hydrogen gas in the reaction chamber. The results have been finally compared to the literature. The study has been made possible by the combination of rapid X-ray detectors with a reaction chamber capable of withstanding gas pressures up to 100 bar and temperatures up to 900 °C.

Preparation, Characterization and Hemostatic Properties of Chitosan Caffeates

2019 ◽  
Vol 814 ◽  
pp. 365-371
Author(s):  
Si Tong Lu ◽  
Dong Ying Zhang ◽  
Zhang Hu ◽  
Si Dong Li ◽  
Pu Wang Li
Keyword(s):  
Caffeic Acid ◽  
Freeze Drying ◽  
Water Solubility ◽  
Crystal Form ◽  
Positive Control ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Yunnan Baiyao ◽  
Better Than

In this paper, chitosan and caffeic acid were used as starting materials to prepare chitosan caffeates by reflux-heating and freeze-drying. The structures of chitosan caffeates were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and potentiometric titration. At the same time, the physical properties of chitosan caffeates were tested and the hemostatic properties were evaluated. The results showed that four chitosan caffeates with different mass ratios of chitosan and caffeic acid (1:1, 1:2, 1:4, 1:6) had been successfully prepared, which enhanced the water solubility. FTIR analysis demonstrated that caffeic acid had been successfully grafted onto chitosan chains. XRD showed that the crystal form of chitosan changed to some extent and the chain had some regularity in some directions, but its crystallinity reduced. Chitosan caffeates, particularly mass ratio of 1:1, showed excellent hemostatic properties and even better than chitosan and the positive control (Yunnan Baiyao), which were expected to be developed as an effective biomaterial for hemostasis.

Large-scale and facile fabrication of PbSe nanostructures by selenization of a Pb sheet

2015 ◽  
Vol 08 (05) ◽  
pp. 1550063 ◽  
Author(s):  
Sara Hoomi ◽  
Ramin Yousefi ◽  
Farid Jamali-Sheini ◽  
Abdolhossein Sáaedi ◽  
Mohsen Cheraghizade ◽  
...  
Keyword(s):  
Large Scale ◽  
Chemical Vapor ◽  
Infrared Region ◽  
Photoelectron Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Facile Fabrication ◽  
Higher Temperature ◽  
Set Up ◽  
Lower Temperature

PbSe nanostructures were synthesized by selenization of lead sheets in a chemical vapor deposition (CVD) set-up under a selenium ambiance. The lead sheets were placed in the different temperature zones, between 300°C and 450°C. Field emission scanning electron microscope (FESEM) images showed that, PbSe nanostructures grown on the lead sheets with different morphologies. PbSe nanostructures with flakes shape were grown on the lead sheets that were placed in the lower temperature, while PbSe nanocubes and nanorods, which were grown on the nanocubes, were grown on the lead sheets in the higher temperature. The phase and composition of the product were identified by X-ray diffraction (XRD) pattern and X-ray photoelectron spectra (XPS). The XRD and XPS results showed that, the PbSe phase was started to form after 350°C and completed at 450°C. However, the XPS results showed that the Se concentration was different in the samples. In addition, Raman measurements confirmed the XRD and XPS results and indicated three Raman active modes, which belonged to PbSe phase for the nanostructures. The optical properties of the products were characterized by UV–Vis. The optical characterization results showed a band gap for the PbSe nanostructures in the infrared region.

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