scholarly journals Natural rubber degradation products: Fine chemicals and reuse of rubber waste

2022 ◽  
pp. 111001
Author(s):  
Franciela Arenhart Soares ◽  
Alexander Steinbüchel
2018 ◽  
Vol 51 (7-8) ◽  
pp. 583-602
Author(s):  
Nabil Hayeemasae ◽  
Hanafi Ismail

This article proposes a new type of magnetorheological elastomer (MRE) based on natural rubber (NR) and waste natural rubber gloves (wNRg) blends. The material properties of the MRE samples were investigated with specific focus on the curing and swelling kinetics. Two different series were prepared; the first used carbonyl iron (CI) as the single filler in the MRE, whereas the second hybridized CI with carbon black (CB) to prepare an MRE resistant to solvents. The results show that most properties depend strongly on the nature of both fillers. The higher thermal conductivity of the CI caused a substantial decrease in both the scorch and curing times and the activation energy in the curing process. Based on the diffusion study, a higher volume of fillers in the rubber composites resulted in a greater area of blockage and restricted the penetration of the solvent tested throughout the composites, irrespective of whether CI alone or in combination with CB was used in the composites.


Polímeros ◽  
2013 ◽  
Vol 23 (4) ◽  
pp. 441-450 ◽  
Author(s):  
Alexander FAINLEIB ◽  
Renata V. PIRES ◽  
Elizabete F. LUCAS ◽  
Bluma G. SOARES

2020 ◽  
Vol 86 (15) ◽  
Author(s):  
Jan de Witt ◽  
Sylvia Oetermann ◽  
Mariana Parise ◽  
Doglas Parise ◽  
Jan Baumbach ◽  
...  

ABSTRACT A cAMP receptor protein (CRPVH2) was detected as a global regulator in Gordonia polyisoprenivorans VH2 and was proposed to participate in the network regulating poly(cis-1,4-isoprene) degradation as a novel key regulator. CRPVH2 shares a sequence identity of 79% with GlxR, a well-studied global regulator of Corynebacterium glutamicum. Furthermore, CRPVH2 and GlxR have a common oligomerization state and similar binding motifs, and thus most likely have similar functions as global regulators. Size exclusion chromatography of purified CRPVH2 confirmed the existence as a homodimer with a native molecular weight of 44.1 kDa in the presence of cAMP. CRPVH2 bound to the TGTGAN6TCACT motif within the 131-bp intergenic region of divergently oriented lcp1VH2 and lcpRVH2, encoding a latex clearing protein and its putative repressor, respectively. DNase I footprinting assays revealed the exact operator size of CRPVH2 in the intergenic region (25 bp), which partly overlapped with the proposed promoters of lcpRVH2 and lcp1VH2. Our findings indicate that CRPVH2 represses the expression of lcpRVH2 while simultaneously directly or indirectly activating the expression of lcp1VH2 by binding the competing promoter regions. Furthermore, binding of CRPVH2 to upstream regions of additional putative enzymes of poly(cis-1,4-isoprene) degradation was verified in vitro. In silico analyses predicted 206 CRPVH2 binding sites comprising 244 genes associated with several functional categories, including carbon and peptide metabolism, stress response, etc. The gene expression regulation of several subordinated regulators substantiated the function of CRPVH2 as a global regulator. Moreover, we anticipate that the novel lcpR regulation mechanism by CRPs is widespread in other rubber-degrading actinomycetes. IMPORTANCE In order to develop efficient microbial recycling strategies for rubber waste materials, it is required that we understand the degradation pathway of the polymer and how it is regulated. However, only little is known about the transcriptional regulation of the rubber degradation pathway, which seems to be upregulated in the presence of the polymer. We identified a novel key regulator of rubber degradation (CRPVH2) that regulates several parts of the pathway in the potent rubber-degrader G. polyisoprenivorans VH2. Furthermore, we provide evidence for a widespread involvement of CRP regulators in the degradation of rubber in various other rubber-degrading actinomycetes. Thus, these novel insights into the regulation of rubber degradation are essential for developing efficient microbial degradation strategies for rubber waste materials by this group of actinomycetes.


2013 ◽  
Vol 773 ◽  
pp. 668-672
Author(s):  
Jun Liang Liu ◽  
Ping Liu ◽  
Xiao Qiang Tang ◽  
Dong Zeng ◽  
Xing Kai Zhang ◽  
...  

In this paper, the blends of natural rubber with waste ground rubber powders have been prepared by mechano-chemical activation method. The influences of particle sizes on both processing performances and mechanical properties have been investigated. The results indicated that: the blends with waste ground rubber powders of smaller particle sizes approached to higher surface tensile and easily mechano-chemical activation, which led to the formation of complete homogenous re-vulcanization cross-linking structure and resulted in the improvements of the whole performances of the final products. The tensile strength, the elongation at break and tear strength approached to the highest value of 20.7MPa, 530% and 33.0 kN/m as the 100mesh waste ground rubber powders were used as the starting materials.


2017 ◽  
Vol 81 (3) ◽  
pp. 614-620 ◽  
Author(s):  
Daisuke Kasai ◽  
Shunsuke Imai ◽  
Shota Asano ◽  
Michiro Tabata ◽  
So Iijima ◽  
...  

2021 ◽  
Vol 59 (3) ◽  
pp. 302
Author(s):  
Nguyen Hoang Dung ◽  
Nguyen Thi Thu Trang ◽  
Nguyen Thi Thanh ◽  
Pham Thi Quynh ◽  
Nguyen Tien Thanh ◽  
...  

The accumulation of rubber waste has become a major environmental issue worldwide due to its adverse effects on ecology. Bioremediation is focused to minimize this problem. In this study, the degradation of deproteinized natural rubber (DPNR) using bacterial consortia enriched from Sapa soil was examined. This soil was not history with rubber. The highest 39.16 ± 1.95 % weight loss of DPNR film was detected in the sixth enrichment consortium after 30 days of incubation. The occurrence of hydroxyl group in the film was observed by Fourier Transform Infrared Spectroscopy analysis. The changes in bacterial community in the consortia were determined by metagenomic analysis using 16S rRNA gene sequencing. The dominant phyla in all consortia were Actinobacteria, Bacteroidetes, and Proteobacteria, while the phylum Actinobacteria was key rubber-degraders in the consortia.


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