A comparative study on the effect of higher acrylate on cross-linkable PMMA used as environment friendly latexes

2020 ◽  
Vol 32 (2) ◽  
pp. 135-141
Author(s):  
Sweta Shukla

The kinetics of emulsion polymerization of monomers methyl methacrylate (MMA)/ n-butyl methacrylate (BMA) was studied to investigate the effect of cross-linkable monomer poly(propylene glycol diacrylate) (PPGDA). The results showed that by the incorporation of PPGDA rate constant of reaction decreased. Fourier transform infrared spectroscopy and scanning electron microscope were used to characterize the synthesized polymers. The thermal analysis of samples was done by differential scanning calorimetry, and the results were compared by the previous studies with MMA/ n-butyl acrylate (BA) and MMA/2-ethylhexyl acrylate (EHA). The glass transition temperature ( T g) values show that the latexes prepared using BA and EHA as comonomer was suitable for binder purpose, but in the present study the T g is not suitable in case of BMA as higher acrylate comonomer. That may be due to more cross-linking in MMA-BMA-PPGDA. The results conclude that the BA and EHA can be used as the binder, but the use of BMA is limited for the binder in coating applications.

Author(s):  
Aslina Br. Ginting ◽  
Supardjo Supardjo ◽  
Yanlinastuti Yanlinastuti ◽  
Dian Anggraini ◽  
Boybul Boybul

Meningkatnya densitas uranium dari 2,96 gU/cm3 menjadi 5,2 gU/cm3 bahan bakar U3Si2/Al harus diikuti dengan penggunaan kelongsong yang kompatibel. Bahan bakar berdensitas tinggi mempunyai kekerasan yang tinggi, sehingga bila menggunakan paduan AlMg2 sebagai kelongsong dapat menyebabkan terjadi dogbone pada saat perolan. Selain fenomena dogbone, pada saat bahan bakar tersebut digunakan di reaktor dapat terjadi swelling karena meningkatnya hasil fisi maupun burn up. Oleh karena itu, perlu dicari pengganti bahan kelongsong untuk bahan bakar U3Si2/Al densitas tinggi. Pada penelitian ini telah dilakukan karakterisasi paduan AlMgSi sebagai kandidat pengganti kelongsong AlMg2. Karakterisasi yang dilakukan meliputi analisis termal, kekerasan, mikrostruktur dan laju korosi. Analisis termal dilakukan menggunakan DTA (Differential Thermal Analysis) dan DSC (Differential Scanning Calorimetry). Analisis kekerasan menggunakan alat uji kekerasan mikro, mikrostruktur menggunakan SEM (Scanning Electron Microscope) dan analisis laju korosi dilakukan dengan pemanasan pada temperatur 150 oC selama 77 jam di dalam autoclave. Hasil analisis menunjukkan bahwa kelongsong AlMgSi maupun AlMg2 mempunyai kompatibilitas panas dengan bahan bakar U3Si2/Al cukup stabil hingga temperatur 650 oC. Kelongsong AlMgSi mempunyai kekerasan sebesar 115 HVN dan kelongsong AlMg2 sebesar 70,1 HVN. Sementara itu, analisis mikrostruktur menunjukkan bahwa morfologi ikatan antarmuka (interface bonding) kelongsong AlMgSi lebih baik dari kelongsong AlMg2, demikian halnya dengan laju korosi bahwa kelongsong AlMgSi mempunyai laju korosi lebih kecil dibanding kelongsong AlMg2. Hasil karakterisasi termal, kekerasan, mikrostruktur dan laju korosi menunjukkan bahwa PEB U3Si2/Al densitas 5,2 gU/cm3 menggunakan kelongsong AlMgSi lebih baik dibanding PEB U3Si2/Al  densitas 5,2 gU/cm3  menggunakan kelongsong AlMg2.Kata kunci: U3Si2/Al, densitas 5,2 gU/cm3, kelongsong AlMgSi dan AlMg2.


CORD ◽  
2013 ◽  
Vol 29 (1) ◽  
pp. 9
Author(s):  
I.D.K. Anom

Thermal and microstructure analysis of cocofoam made from vulcanized coconut fiber and latex compound were conducted. The cocofoam was produced by blending coconut fiber and latex compound with weight ratio of 10/25 (CF5-1) and 20/55 (CF5-2) at room temperature. The cocofoam characters were then analyzed by Scanning Electron Microscope (SEM), Thermogravimetric Analysis (TGA) and Differential Scanning Calorimetry (DTA) instruments. The result showed that the increase of coconut fiber and latex compound ratio produced a higher density of cocofoam. The highest value density was 0.6920 g/cm3 with flexibility of 90% produced by the CF5-2 sample. The SEM analysis showed that both specimens surface of the CF5-1 and CF5-2 samples have different pores size and the latex compound is not distributed thoroughly in the cocofoam. The thermal analysis showed that the production of cocofoam was largely determined by latex compound that served as fiber binder matrix. Cocofoam started to degrade at the temperature of 90oC and was damaged when it was heated at the temperature of 115oC for 2.5 hours.


Materials ◽  
2021 ◽  
Vol 14 (19) ◽  
pp. 5535
Author(s):  
Piotr Kobędza ◽  
Aleksandra Smejda-Krzewicka ◽  
Krzysztof Strzelec

The purpose of this work was to verify the ability to cross-link the chloroprene rubber (CR) by using copper oxides: copper(I) oxide or copper(II) oxide. The use of copper oxides arises from the need to limit the application of ZnO as a cross-linking agent of CR. The obtained results indicate that CR compositions cross-linked with copper oxides are characterized by good mechanical properties and a high cross-linking degree. The results show that the type and the amount of copper oxides influence the cross-linking of the CR and the properties of the vulcanizates. For compositions containing copper(II) oxide, the properties are linearly dependent on the amount of CuO. Such a relationship is difficult to notice in the case of the use of copper(I) oxide—when analyzing individual parameters, the best results are obtained for different samples. Infrared spectroscopy (IR) studies confirmed the possibility of cross-linking of chloroprene rubber with copper oxides. This is evidenced by the characteristic changes in the intensity of the bands. Structural changes in the material during heating were determined by the thermal analysis—differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Regardless of the type and amount of copper oxide, all compositions exhibit similar characteristics, and there are no significant changes in the glass transition temperature of the material.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Nurul Fatahah Asyqin Zainal ◽  
Jean Marc Saiter ◽  
Suhaila Idayu Abdul Halim ◽  
Romain Lucas ◽  
Chin Han Chan

AbstractWe present an overview for the basic fundamental of thermal analysis, which is applicable for educational purposes, especially for lecturers at the universities, who may refer to the articles as the references to “teach” or to “lecture” to final year project students or young researchers who are working on their postgraduate projects. Description of basic instrumentation [i.e. differential scanning calorimetry (DSC) and thermogravimetry (TGA)] covers from what we should know about the instrument, calibration, baseline and samples’ signal. We also provide the step-by-step guides for the estimation of the glass transition temperature after DSC as well as examples and exercises are included, which are applicable for teaching activities. Glass transition temperature is an important property for commercial application of a polymeric material, e.g. packaging, automotive, etc. TGA is also highlighted where the analysis gives important thermal degradation information of a material to avoid sample decomposition during the DSC measurement. The step-by-step guides of the estimation of the activation energy after TGA based on Hoffman’s Arrhenius-like relationship are also provided.


Author(s):  
Kinga Tamási ◽  
Kálmán Marossy

AbstractThe paper deals with the study of seven selected natural plant oils. Differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA) and thermally stimulated discharge (TSD) methods were used. It has been found that most of the oils tested are in a glassy state at low temperature and have multiple transitions in the low temperature range. DSC shows complex melting-like processes or glass transition. For both DMA and TSD, the scaffold supportive method was used and found as a suitable one. DMA and TSD proved more sensitive than DSC and revealed at least two transitions between − 120 and − 40 °C. In the case of three oils (argan, avocado and sunflower), current reversal was observed by TSD; this symptom cannot be fully explained at the moment.


Polymers ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 270
Author(s):  
Evgeniy V. Belukhichev ◽  
Vera E. Sitnikova ◽  
Evgenia O. Samuylova ◽  
Mayya V. Uspenskaya ◽  
Daria M. Martynova

Polymeric packaging materials are one of the factors of environmental pollution. Reducing the environmental burden is possible by increasing the environmental friendliness of packaging materials. In this work, we study polymer films based on polyvinyl chloride (PVC) with a copolymer of 3-hydroxybutyrate with 3-hydroxyhexanoate P (3-GB) (3-GG) with different component ratios. The process of processing blends in the process of obtaining a packaging film is considered. The optical characteristics of the obtained films are determined. Thermal analysis of the obtained films was carried out using the differential scanning calorimetry (DSC), TGA, and thermomechanical analysis (TMA) methods. The degree of gelling of the resulting mixture was determined. It is shown that PHB has miscibility with PVC.


2021 ◽  
pp. 095400832110055
Author(s):  
Yang Wang ◽  
Yuhui Zhang ◽  
Yuhan Xu ◽  
Xiucai Liu ◽  
Weihong Guo

The super-tough bio-based nylon was prepared by melt extrusion. In order to improve the compatibility between bio-based nylon and elastomer, the elastomer POE was grafted with maleic anhydride. Scanning Electron Microscopy (SEM) and Thermogravimetric Analysis (TGA) were used to study the compatibility and micro-distribution between super-tough bio-based nylon and toughened elastomers. The results of mechanical strength experiments show that the 20% content of POE-g-MAH has the best toughening effect. After toughening, the toughness of the super-tough nylon was significantly improved. The notched impact strength was 88 kJ/m2 increasing by 1700%, which was in line with the industrial super-tough nylon. X-ray Diffraction (XRD) and Differential Scanning Calorimetry (DSC) were used to study the crystallization behavior of bio-based PA56, and the effect of bio-based PA56 with high crystallinity on mechanical properties was analyzed from the microstructure.


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