scholarly journals Hazardous Waste Management of Buffing Dust Collagen

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1498
Author(s):  
Miroslawa Prochon ◽  
Anna Marzec ◽  
Oleksandra Dzeikala

Buffing Dust Collagen (BDC) is a hazardous waste product of chromium tanning bovine hides. The aim of this study was to investigate whether BDC has the desirable properties required of modern fillers. The microstructural properties of BDC were characterized by elemental analysis (N, Cr2O3) of dry residue and scanning electron microscopy (SEM). The BDC was applied (5 to 30 parts by weight) to styrene butadiene rubber (SBR), obtaining SBR-BDC composites. The physicochemical properties of the SBR-BDC composites were examined by Fourier transform infrared analysis, SEM, UV–Vis spectroscopy, swelling tests, mechanical tests, thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The biodegradability of the SBR-BDC composites and their thermo-oxidative aging were also investigated. The filler contributed to increase the cross-link density in the elastomer structure, as evidenced by enhanced mechanical strength. The introduction of a filler into the elastomer structure resulted in an increase in the efficiency of polymer bonding, which was manifested by more favorable rheological and mechanical parameters. It also influenced the formation of stable interfacial bonds between the individual components in the polymer matrix, which in turn reduced the release of compact chromium in the BDC filler. This was shown by the absorption bands for polar groups in the infrared analysis and by imaging of the vulcanization process.

Materials ◽  
2019 ◽  
Vol 12 (10) ◽  
pp. 1684 ◽  
Author(s):  
Mirosława Prochoń ◽  
Anna Marzec ◽  
Bolesław Szadkowski

The purpose of this work was to prepare new biodegradable starch-cellulose composites, with starch, using casein and gelatin as natural nutrients. The physico-chemical properties of the starch films and cellulose fabrics with starch coatings were studied by Fourier transformation infrared analysis, laser confocal scanning microscopy (LCSM), scanning electron microscopy (SEM), UV-Vis spectroscopy, swelling tests, mechanical tests, thermal analysis thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The susceptibility of the starch films to biodegradation was investigated, together with their resistance to thermo-oxidative aging. As a result of the formation of the starch films, both the casein and gelatin macromolecules were able to interact directly with the starch matrix and the fractions of unbranched amylose and branched amylopectin it contained. This interaction was visible as changes in the absorption bands of the polar groups, as revealed by infrared analysis. Spectral analysis of the cellulose fabrics coated with starch films suggests that hydrogen bridges formed between the micelles of long cellulose filaments and the micro and macro-fibers of the starch pectins. An applicative test revealed that when used as a covering for bean cultivation the cellulose-starch composites act as a fertilizing component, contributing to significantly improved growth of Phaseolus vulgaris in comparison to the use of unmodified cellulose.


1970 ◽  
Vol 43 (6) ◽  
pp. 1332-1339 ◽  
Author(s):  
J. K. Clark ◽  
R. A. Scott

Abstract Dissolution of sulfur-cured, carbon black-loaded copolymers and their blends with cis-1,4-polybutadiene (PBD) are brought about by boiling with o-dichlorobenzene which contains a small amount of 2,2′-dibenzamidodiphenyl disulfide. The resulting slurries are subjected to a sequence of separations which include high-speed centrifugation to remove solids, and solvent precipitation followed by filtration to isolate the precipitates. The precipitates are washed with solvent to remove soluble organic materials followed by carbon disulfide washing to dissolve the polymers. Cast films of the polymers are obtained by evaporating the carbon disulfide washings onto sodium chloride discs. The infrared spectra of the cast films of these preparations are very similar to those of their respective polymers prior to loading and curing. Calculations for relative concentrations of bound styrene and PBD micro-structures permit nominal identification of the kinds of styrene-butadiene rubber and the amounts of cis-1,4-PBD used in a cured rubber formulation. Absorption bands used are near 3.35 μ for cis-1,4-PBD, 6.65 μ for bound styrene, 10.35 μ for trans-1,4-PBD; and 11.0 μ for vinyl-1,2-PBD. Efforts are being made to improve the data by using a grating infrared instrument and also to extend the calibrations to include other rubber blends.


2020 ◽  
pp. 009524432093398
Author(s):  
Fuquan Deng ◽  
Hua Jin ◽  
Li Zhang ◽  
Yuxin He

Polymeric foam with lightweight and higher impact strength has been used in many fields due to cost reduction and higher toughness. However, it is often difficult to improve their mechanical property especially tear strength. Here, a double foaming system was designed to increase the tear strength of the foamed ethylene–propylene–diene monomer, styrene–butadiene rubber, and thermoplastic rubber (EPDM/SBR/TPR) materials. The cell size of EPDM/SBR/TPR foam and cell distribution were investigated by scanning electron microscopy, which showed that the cells present a bimodal structure. Besides, the tear strength can reach up to 10 N/mm when the density is about 0.40 g/cm3, which is much superior to those of most engineering plastic foams. Meanwhile, the crystallization property of EPDM/SBR/TPR foams was also demonstrated by X-ray diffraction, thermogravimetric analysis, and differential scanning calorimetry, which indicates that the double foaming system can reduce the crystallization of EPDM/SBR/TPR molecular chains. In addition, the variation of thermal conductivity values depends on the gradual decrease effect of the cell size.


2019 ◽  
pp. 000-000
Author(s):  
Qing-Yuan Han ◽  
Xu Li ◽  
Yu-Chun Li ◽  
You-Ping Wu

ABSTRACT The compatibility between solution polymerized styrene–butadiene rubber (SSBR 2466) and natural rubber (NR) is characterized by differential scanning calorimetry and dynamic mechanical thermal analysis. The single glass transition in the entire temperature range of all NR/SSBR blends and good correlation between Tg and SSBR fraction prove the excellent compatibility between SSBR 2466 and NR. With increasing SSBR content, a reduced Payne effect, more homogeneous dispersion of silica, stronger rubber–filler interaction, and more silica selectively distributed in the SSBR phase were determined via rubber-processing analysis, transmission electron microscopy, bound rubber, and thermogravimetric analysis, respectively. The high vinyl content, low styrene content, and end-functionalized structure of SSBR play vital roles in promoting its compatibility with NR and a stronger rubber–silica linkage. The resulting increased tan δ at 0 °C and low tan δ at 60 °C indicates good wet-skid resistance and low rolling resistance by blending SSBR 2466, and 70/30 NR/SSBR is the best balance for producing a “green tire” tread.


e-Polymers ◽  
2007 ◽  
Vol 7 (1) ◽  
Author(s):  
Mahdi Abdollahi ◽  
Ali Rahmatpour ◽  
Jamal Aalaie ◽  
Homayon Hossein Khanli

AbstractStyrene- butadiene rubber (SBR)/ clay nanocomposites were prepared by mixing the SBR latex with aqueous clay dispersion and co-coagulating the mixture. Tapping mode AFM and XRD were applied to characterize the structure of nanocomposites. It was found that fully exfoliated structure could be obtained by this method only when the low loading of layered silicate (< 10 phr) is used. With increasing the clay content, both non-exfoliated (stacked layers) and exfoliated structures can be observed simultaneously in the nanocomposites. The results of mechanical tests on the vulcanized pure SBR and SBR/ clay nanocomposites showed that the nanocomposites presents better mechanical properties than clayfree SBR vulcanizate. Furthermore, initial modulus, tensile strength, tensile strain at break, hardness (shore A) and tear strength increased with increasing the clay content, indicating the nanoreinforcement effect of clay on the mechanical properties of SBR/ clay nanocomposites. Compared to the clay free SBR vulcanizate, the nanocomposite vulcanizates exhibit a lower tanδ peak value, higher storage modulus and higher tanδ value at the rubbery region (0-60 °C) which indicate that the elastic responses of pure SBR towards deformation are strongly influenced by the presence of nanodisperced natural sodium montmorillonite layers especially completely exfoliated silicate layers.


2016 ◽  
Vol 49 (4) ◽  
pp. 298-314 ◽  
Author(s):  
Sara Estagy ◽  
Saeed Ostad Movahed ◽  
Soheil Yazdanbakhsh ◽  
Majid Karim Nezhad

The market for commercial polymer blends has grown steadily. A good blend should have strong interphases between different parts of the constituted polymers. Lack of strong interphases is a classical problem of the blend industry. Ethylene-propylene-diene monomer rubber (EPDM)/styrene-butadiene rubber (SBR) blends have a very good aging resistance and good compression sets. However, these rubbers are partially miscible. To improve the miscibility of EPDM and SBR in their blends, a Lewis acid, AlCl3, was used to form EPDM–g–SBR copolymer through Friedel–Crafts reactions. The existence of covalent bonds between EPDM and SBR macromolecules was studied by the cure traces of the blends, that is, ΔTorque, Fourier transform infrared spectrums, differential scanning calorimetry (DSC) heat flow curves, thermogravimetric analysis curves, and scanning electron (SEM) micrographs. Subsequently, several blends with EPDM/SBR ratio of 40/60 and with various AlCl3 amounts were prepared and after curing, their mechanical properties were measured and compared. The results showed covalent bonds formed between SBR–EPDM and SBR–SBR macromolecules. An exothermic change in heat flow in the DSC curve was observed around 111.28°C, which can be attributed to the formation of carbocations in Friedel–Crafts reactions. Adding 2 phr AlCl3 had an efficient effect on EPDM–SBR and or SBR–SBR linkages. The mechanical properties of the cured blends, that is, tensile strength were lower when compared with corresponding values for prepared compound with SBR. Excellent compatibility between the two polymers and strong interphases were observed in SEM micrograph of the cured blend with 1 phr AlCl3.


Minerals ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1388
Author(s):  
Kenan Zhang ◽  
Hao Zhang ◽  
Linsong Liu ◽  
Yongjie Yang ◽  
Lihui Liu ◽  
...  

The aim of this work was to investigate the dispersibility of kaolinite-rich coal gangue in rubber matrix, the mechanical properties and thermal stability of coal gangue/styrene butadiene rubber (SBR) composites, and to compare these properties to those of the same coal gangue but had undergone thermal activation and modification. Several experimental techniques, such as X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric-differential scanning calorimetry (TG-DSC), laser-scattering particle analyzer were adopted to characterize the coal gangue particles and then the obtained composites. The results demonstrated the raw coal gangue (RCG) was mainly composed of kaolinite. Calcination led to amorphization of thermal activated coal gangue (ACG), increased hydrophilicity and void volume, and decreased pH. The grain size of ACG became coarser than RCG, but ACG turned loose confirmed by higher degree of refinement after grinding. Modification enhanced the hydrophobicity of the coal gangue and improved its dispersibility than fillers without modification. Calcined samples had better dispersibility than uncalcined fillers. Additionally, the coal gangue treated by calcinating, grinding and modifying (MGA) had the best dispersion in rubber matrix. Either calcination or modification could improve the mechanical properties and thermal stability of coal gangue filled rubber, while the performance of MGA reinforced SBR (MGA-SBR) was the best. The enhanced performance of the MGA-SBR was owed to better dispersion of particles as well as stronger interactions between particles and rubber macromolecules.


Materials ◽  
2021 ◽  
Vol 14 (23) ◽  
pp. 7304
Author(s):  
Chaohua Zhao ◽  
Xiaoyao Jia ◽  
Zhijian Yi ◽  
Hualin Li ◽  
Yi Peng

Polymer-modified cement has found numerous applications due to its excellent tensile strength. When cement was modified with a single polymer, its tensile strength and performance marginally increased. However, when a small amount of the flexible polymer latex was added to cement, the mechanical performance of cement considerably improved. In this study, single-graded copolymer-modified pervious concrete was prepared by mixing styrene-butadiene rubber (SBR) with different acrylate polymers, and its mechanical performance and durability were systematically studied through mechanical tests and theoretical analyses. The main findings are as follows: (1) When a waterborne emulsion was added, the freeze resistance of cement concrete increased, and its mass loss rate decreased. Cement concrete with two latexes had higher sulphate corrosion resistance and substantially lower dry shrinkage strain than ordinary cement concrete. (2) Through scanning electron microscopy, the microstructural changes in the cement binder, ordinary polymer-modified concrete, and the copolymer-modified cement concrete used in this study were observed, and the findings were compared with those reported in the literature. (3) Single-graded copolymer-modified pervious concrete exhibited excellent shrinkage performance. This study showed that single-graded copolymer-modified pervious concrete satisfied the performance requirements for use as a paving material for special cases.


2019 ◽  
Vol 92 (1) ◽  
pp. 69-89 ◽  
Author(s):  
Katarzyna S. Bandzierz ◽  
Louis A. E. M. Reuvekamp ◽  
Jerzy Dryzek ◽  
Wilma K. Dierkes ◽  
Anke Blume ◽  
...  

ABSTRACT Considerable attention is paid to the influence of crosslink density and crosslink structures on the behavior of polymer chains and properties of elastomers. However, a very important parameter seems to be underestimated: the modifications to the polymer chains by curatives, formed by sulfur and fragments of accelerators. We draw attention to this important contribution to performance of spatial networks. The emulsion styrene–butadiene rubber samples, cured with tetramethylthiuram disulfide and sulfur (TMTD/S8) and zinc dialkyl dithiophosphate with sulfur (ZDT/S8), were studied. They were characterized in detail in terms of crosslink density and crosslink structures. Microscale techniques were used to obtain information about the behavior of the polymer chains: positron annihilation lifetime spectroscopy (PALS) to study the free volume structure and differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) to monitor the glass transition process. Properties such as static mechanical performance and thermo-oxidative stability were also evaluated. All of the investigated characteristics were influenced by a combination of crosslink density, crosslink structures, and, to a large extent, by the modifications of the polymer chains. The effect of the modifications is dependent on the amount and the structure of the curatives' molecules. On the basis of the obtained results, the usefulness of the “phr” unit used for calculation of the curatives' amount has been queried. Furthermore, it has been demonstrated that DSC, DMA, and PALS techniques can provide evidence for the presence of the modifications on the polymer chain by curatives.


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