Pyrolysis of Denim Jeans Waste: Pyrolytic Product Modification by the Addition of Sodium Carbonate.

Quickly changing fashion trends generate tremendous amounts of textile waste globally. The inhomogeneity and complicated nature of textile waste make its recycling challenging. Hence, it is urgent to develop a feasible method to extract value from textile waste. Pyrolysis is an effective waste-to-energy option to processing waste feedstocks having an inhomogeneous and complicated nature. Herein, pyrolysis of denim jeans waste (DJW; a textile waste surrogate) was performed in a continuous flow pyrolyser. The effects of adding sodium carbonate (Na2CO3; feedstock/Na2CO3 = 10, weight basis) to the DJW pyrolysis on the yield and composition of pyrolysates were explored. For the DJW pyrolysis, using Na2CO3 as an additive increased the yields of gas and solid phase pyrolysates and decreased the yield of liquid phase pyrolysate. The highest yield of the gas phase pyrolysate was 34.1 wt% at 800 °C in the presence of Na2CO3. The addition of Na2CO3 could increase the contents of combustible gases such as H2 and CO in the gas phase pyrolysate in comparison with the DJW pyrolysis without Na2CO3. The maximum yield of the liquid phase pyrolysate obtained with Na2CO3 was 62.5 wt% at 400 °C. The composition of the liquid phase pyrolysate indicated that the Na2CO3 additive decreased the contents of organic acids, which potentially improve its fuel property by reducing acid value. The results indicated that Na2CO3 can be a potential additive to pyrolysis to enhance energy recovery from DJW.

Single-Use Disposable Waste Upcycling via Thermochemical Conversion Pathway.

Herein, the pyrolysis of two types of single-use disposable waste (single-use food containers and corrugated fiberboard) was investigated as an approach to cleanly dispose of municipal solid waste, including plastic waste. For the pyrolysis of single-use food containers or corrugated fiberboard, an increase in temperature tended to increase the yield of pyrolytic gas (i.e., non-condensable gases) and decrease the yield of pyrolytic liquid (i.e., a mixture of condensable compounds) and solid residue. The single-use food container-derived pyrolytic product was largely composed of hydrocarbons with a wide range of carbon numbers from C1 to C32, while the corrugated fiberboard-derived pyrolytic product was composed of a variety of chemical groups such as phenolic compounds, polycyclic aromatic compounds, and oxygenates involving alcohols, acids, aldehydes, ketones, acetates, and esters. Changes in the pyrolysis temperature from 500 °C to 900 °C had no significant effect on the selectivity toward each chemical group found in the pyrolytic liquid derived from either the single-use food containers or corrugated fiberboard. The co-pyrolysis of the single-use food containers and corrugated fiberboard led to 6 times higher hydrogen (H2) selectivity than the pyrolysis of the single-use food containers only. Furthermore, the co-pyrolysis did not form phenolic compounds or polycyclic aromatic compounds that are hazardous environmental pollutants (0% selectivity), indicating that the co-pyrolysis process is an eco-friendly method to treat single-use disposable waste.

Achievements in pyrolysis process in E-waste management sector.

Many aspects of modern life of our civilization are associated with using electrical and electronic devices (EEE). Ever-increasing demand for high-performance EEE and accelerated technological development make the replacement of EEE become frequent. This leads to the generation of a tremendous amount of electronic waste (E-waste). Challenges of the management of E-waste have recently arisen out of a dearth of proper technologies to treat E-waste. Pyrolysis process can thermochemically treat waste materials that have a complicated nature and inhomogeneity. This article gives a systematic review as an effort to tackle the challenges in the context of achievements in pyrolysis process in E-waste management sector. Pyrolysis mechanism and types of pyrolysis processes and pyrolysis reactors are first discussed. Various pyrolysis technologies applied to the E-waste treatment are then summarized and compared to each other. Points to be considered for further research and pending challenges of E-waste pyrolysis are also discussed. The pyrolysis treatment of E-waste is not yet fully industrialized mostly because of high costs. However, there should be much room for further developing the E-waste pyrolysis; hence, its industrialization and commercialization is just a matter of time.

Waste-to-Fuels: Pyrolysis of Low-Density Polyethylene Waste in the Presence of H-ZSM-11.

Herein, the pyrolysis of low-density polyethylene (LDPE) scrap in the presence of a H-ZSM-11 zeolite was conducted as an effort to valorize plastic waste to fuel-range chemicals. The LDPE-derived pyrolytic gas was composed of low-molecular-weight aliphatic hydrocarbons (e.g., methane, ethane, propane, ethylene, and propylene) and hydrogen. An increase in pyrolysis temperature led to increasing the gaseous hydrocarbon yields for the pyrolysis of LDPE. Using the H-ZSM-11 catalyst in the pyrolysis of LDPE greatly enhanced the content of propylene in the pyrolytic gas because of promoted dehydrogenation of propane formed during the pyrolysis. Apart from the light aliphatic hydrocarbons, jet fuel-, diesel-, and motor oil-range hydrocarbons were found in the pyrolytic liquid for the non-catalytic and catalytic pyrolysis. The change in pyrolysis temperature for the catalytic pyrolysis affected the hydrocarbon compositions of the pyrolytic liquid more materially than for the non-catalytic pyrolysis. This study experimentally showed that H-ZSM-11 can be effective at producing fuel-range hydrocarbons from LDPE waste through pyrolysis. The results would contribute to the development of waste valorization process via plastic upcycling.

Vitamin A deficiency induces fluid hyposecretion from the airway submucosal glands of mice.

Vitamin A deficiency (VAD) alters the phenotype of airway epithelium and attenuates the epithelial defense system, and many studies have reported the association of VAD with respiratory disease. In this study, we investigated changes in submucosal glands (SMG) in a mouse model of VAD. C57BL/6 mice were fed a vitamin A-devoid diet and the others were fed a control diet (1.2 mg retinol/kg). The areas of serous and mucous cells of SMG were measured in 4-, 8-, and 20-wk-old male mice. The volume and lysozyme concentration of glandular secretions were also measured. The 2 groups did not differ in body weight or general morbidity at 3-10 wk of age, although serum retinol concentrations were greater in the control mice than in the VAD mice after 4 wk. Upon histological evaluation, we found that the areal ratio of serous cells:total SMG cells was significantly lower after 8 wk in the VAD mice compared with the control mice, although the total area of SMG did not differ between groups throughout the 20-wk experiment. The number of secretory bubbles did not differ between the groups, but total secretion volume was reduced by 35% in 8-wk-old VAD mice compared with controls. Furthermore, the concentration of lysozyme in secretions from 8-wk-old VAD mice was also less than in controls, compounding the effect of diminished secretion volume. In this study, we found serous cell hypotrophy/hypoplasia and dysfunction in VAD mice, which may contribute to the susceptibility to airway infection linked to VAD.

Dual oxidase 2 is essential for the toll-like receptor 5-mediated inflammatory response in airway mucosa.

AIMS: Airway mucosa is constantly exposed to various airborne microbes, and epithelial host defense requires a robust innate immunity. Recently, it has been suggested that NADPH oxidase (NOX) isozymes serve functional roles in toll-like receptor (TLR)-mediated innate immune responses. However, the molecular mechanism between TLR and NOX-mediated reactive oxygen species (ROS) production in human airway mucosa has been poorly understood. RESULTS: Here, we show that flagellin-induced ROS generation is dependent on dual oxidase 2 (DUOX2) activation, which is regulated by [Ca(2+)](i) mobilization in primary normal human nasal epithelial (NHNE) cells. Interestingly, we observed that silencing of DUOX2 expression in NHNE cells and nasal epithelium of Duox2 knockout mice failed to trigger mucin and MIP-2? production upon challenging flagellin. INNOVATION: Our observation in this study reveals that flagellin-induced hydrogen peroxide (H(2)O(2)) generation is critical for TLR5-dependent innate immune responses, including IL-8 production and MUC5AC expression in the nasal epithelium. Furthermore, DUOX2-mediated H(2)O(2) generation activated by the flagellin-TLR5 axis might serve as a novel therapeutic target for infectious inflammation diseases in the airway tract. CONCLUSION: Taken together, we propose that DUOX2 plays pivotal roles in TLR5-dependent inflammatory response of nasal airway epithelium.

α-Melanocyte-stimulating hormone inhibits tumor necrosis factor α-stimulated MUC5AC expression in human nasal epithelial cells.

Mucin hypersecretion is an important clinical feature of several respiratory diseases, including asthma, cystic fibrosis, nasal allergy, rhinitis, and sinusitis. It has been shown that α-melanocyte-stimulating hormone (α-MSH), a proopiomelanocortin (POMC)-derived peptide, has immunomodulatory activities by inhibiting NF-κB activation induced by proinflammatory cytokines such as TNF-α. Because MUC5AC expression is known to be up-regulated by TNF-α via NF-κB activation, we evaluated the inhibitory effect of α-MSH on MUC5AC gene expression induced by TNF-α in normal human nasal epithelial (NHNE) cells. Melanocortin-1-receptor (MC-1R) was detected by RT-PCR, Western blotting, and immunofluorescent labeling in NHNE cells. α-MSH suppressed NF-κB/p65 phosphorylation induced by TNF-α as well as IkB-α degradation in a dose-dependent manner, as assessed by Western blotting. In addition, α-MSH inhibited TNF-α-induced nuclear translocation of NF-κB and NF-κB luciferase activity. Real-time quantitative PCR data showed that α-MSH inhibited TNF-α-induced expression of MUC5AC, and this effect of α-MSH was neutralized by knockdown of MC-1R using MC-1R shRNA lentivirus. Analyses using RT-PCR and Western blotting showed the expression of POMC and two key enzymes in the POMC processing, proprotein convertases (PC)1 and PC2, and 7B2, which is required for enzymatic activity of PC2, in normal human nasal mucosa. We conclude that α-MSH down-regulates MUC5AC expression by inhibiting TNF-α-induced NF-κB activity through MC-1R stimulation in NHNE cells and that normal human nasal mucosa possesses the POMC processing machinery. Therefore, α-MSH may be a promising candidate to decrease mucin overproduction initiated by NF-κB activation.

Different signaling and cell death roles of heterotrimeric G protein alpha and beta subunits in the Arabidopsis oxidative stress response to ozone.

Arabidopsis thaliana plants with null mutations in the genes encoding the alpha and beta subunits of the single heterotrimeric G protein are less and more sensitive, respectively, to O3 damage than wild-type Columbia-0 plants. The first peak of the bimodal oxidative burst elicited by O3 in wild-type plants is almost entirely missing in both mutants. The late peak is normal in plants lacking the Gbeta protein but missing in plants lacking the Galpha protein. Endogenous reactive oxygen species (ROS) are first detectable in chloroplasts of leaf epidermal guard cells. ROS production in adjacent cells is triggered by extracellular ROS signals produced by guard cell membrane-associated NADPH oxidases encoded by the AtrbohD and AtrbohF genes. The late, tissue damage-associated component of the oxidative burst requires only the Galpha protein and arises from multiple cellular sources. The early component of the oxidative burst, arising primarily from chloroplasts, requires signaling through the heterotrimer (or the Gbetagamma complex) and is separable from Galpha-mediated activation of membrane-bound NADPH oxidases necessary for both intercellular signaling and cell death.