A Janus Textile with Tunable Heating Modes toward Precise Personal Thermal Management in Cold Conditions.

Passive heating textiles (PHTs) have drawn increasing attention due to the advantages of energy-conservation heating. However, the heating capabilities of current PHTs are typically static and non-tunable, presenting poor adaptation to dynamic winter. Herein, a novel Janus textile with tunable heating modes is developed by constructing a customized structure with asymmetric optical properties. This Janus textile is created by coating one side of a cotton fabric with silver nanowires (AgNWs) and then applying transition metal carbides/nitrides (MXene) to the other side. The MXene side exhibits high solar absorptivity and low mid-infrared emissivity, while the AgNWs side has moderate solar absorptivity and mid-infrared emissivity. This structure ensures that the solar and radiative heating temperatures of the MXene side are 16 °C and 1.7 °C higher than those of the AgNWs side. This distinction allows for on-demand, accurate adjustments in solar and radiative heating capabilities by flipping the textile according to ambient temperature. Furthermore, this innovative design also features desired electric heating, thermal camouflage, self-cleaning and antibacterial properties, electromagnetic interference shielding, durability, and wearability. The Janus textile enables precise thermoregulation of the human body to adapt to variable cold weather, making it essential for optimal personal thermal management and climate change mitigation.

A Scalable and Robust Personal Health Management Textile with Multiple Desired Thermal Functions and Electromagnetic Shielding.

The development of functional textiles combining conventional apparel with advanced technologies for personal health management (PHM) has garnered widespread attention. However, the current PHM textiles often achieve multifunctionality by stacking functional modules, leading to poor durability and scalability. Herein, a scalable and robust PHM textile is designed by integrating electrical, radiative, and solar heating, electromagnetic interference (EMI) shielding, and piezoresistive sensing performance onto cotton fabric. This is achieved through an uncomplicated screen-printing process using silver paste. The conductivity of the PHM textile is ≈1.6  ×  104 S m-1, ensuring an electric heating temperature of ≈134 °C with a low voltage of 1.7 V, as well as an EMI shielding effectiveness of ≈56 dB, and human motion monitoring performance. Surprisingly, the radiative/solar heating capability of the PHM textile surpasses that of traditional warm leather. Even after undergoing rigorous physical and chemical treatments, the PHM textile maintains terrific durability. Additionally, the PHM textile possesses maneuverable scalability and comfortable wearability. This innovative work opens up new avenues for the strategic design of PHM textiles and provides an advantageous guarantee of mass production.

Biosorption and degradation of decabromodiphenyl ether by Brevibacillus brevis and the influence of decabromodiphenyl ether on cellular metabolic responses.

There is global concern about the effects of decabromodiphenyl ether (BDE209) on environmental and public health. The molecular properties, biosorption, degradation, accumulation, and cellular metabolic effects of BDE209 were investigated in this study to identify the mechanisms involved in the aerobic biodegradation of BDE209. BDE209 is initially absorbed by wall teichoic acid and N-acetylglucosamine side chains in peptidoglycan, and then, BDE209 is transported and debrominated through three pathways, giving tri-, hepta-, octa-, and nona-bromodiphenyl ethers. The C-C bond energies decrease as the number of bromine atoms on the diphenyl decreases. Polybrominated diphenyl ethers (PBDEs) inhibit protein expression or accelerate protein degradation and increase membrane permeability and the release of Cl(-), Na(+), NH4 (+), arabinose, proteins, acetic acid, and oxalic acid. However, PBDEs increase the amounts of K(+), Mg(2+), PO4 (3-), SO4 (2-), and NO3 (-) assimilated. The biosorption, degradation, accumulation, and removal efficiencies when Brevibacillus brevis (1 g L(-1)) was exposed to BDE209 (0.5 mg L(-1)) for 7 days were 7.4, 69.5, 16.3, and 94.6 %, respectively.

Biosorption and biodegradation of triphenyltin by Stenotrophomonas maltophilia and their influence on cellular metabolism.

Triphenyltin (TPT), an endocrine disruptor, is polluting the global environment through its worldwide use. However, information concerning the mechanisms of TPT biodegradation and cellular metabolism is severely limited. Therefore, these processes were elucidated through experiments involving TPT biosorption and degradation, intracellular metabolite analysis, nutrient use, ion and monosaccharide release, cellular membrane permeability and protein concentration quantification. The results verified that TPT was initially adsorbed by the cell surface of Stenotrophomonas maltophilia and was subsequently transported and degraded intracellularly with diphenyltin and monophenyltin production. Cl(-), Na(+), arabinose and glucose release, membrane permeability and the extracellular protein concentration increased during TPT treatment, whereas K(+) and PO4(3-) utilization and intracellular protein concentration declined. The biosorption, degradation and removal efficiencies of TPT at 0.5mgL(-1) by 0.3gL(-1) viable cells at 10 d were 3.8, 77.8 and 86.2%, respectively, and the adsorption efficiency by inactivated cells was 72.6%.

Triphenyltin biodegradation and intracellular material release by Brevibacillus brevis.

Triphenyltin (TPT) is an endocrine disruptor that has polluted the global environment, and thus far, information regarding the mechanisms of TPT biodegradation and intracellular material release is limited. Here, TPT biodegradation was conducted by using Brevibacillus brevis. Degradation affecting factors, metabolite formation, ion and protein release, membrane permeability, and cell viability after degradation were investigated to reveal the biodegradation mechanisms. The results showed that TPT could be degraded simultaneously to diphenyltin and monophenyltin, with diphenyltin further degraded to monophenyltin, and ultimately to inorganic tin. During degradation process, B. brevis metabolically released Cl(-) and Na(+), and passively diffused Ca(2+). Protein release and membrane permeability were also enhanced by TPT exposure. pH ranging from 6.0 to 7.5 and relatively high biomass dosage in mineral salt medium improved TPT degradation. Biodegradation efficiency of 0.5 mg L(-1) TPT by 0.3 g L(-1)B. brevis at 25 °C for 5d was up to 80%.

[Enhancing effect of Tween 80 on degradation of triphenyltin by Bacillus thuringiensis].

So far, the information regarding enhanced degradation and biodegradation mechanisms of TPhT, an endocrine disruptor, is severely limited. Whether dearylation during TPhT degradation occurs successively or synchronously is not revealed clearly. To deal with these problems, this study focused on the biodegradation of TPhT and its metabolites by Bacillus thuringiensis through the acceleration of Tween 80. The results showed that Tween 80 obviously increased the TPhT solubility. After degradation by cells in the presence of 80 mg L-1 Tween 80 for 2 d, the residual TPhT at 1 mg L-1 initially was decreased to 48.4%. During the biodegradation process, Tween 80 significantly reduced intracellular Na+, NH+4: and Mg2+ release, and increased extracellular Cl- , PO(3-)4 and K+ utilization. Metabolites analysis revealed that phenyltin biodegradation initially proceeded by cleaving the aromatic ring, not by splitting the covalent bonds between the benzene rings and tin atom. Ring-cleavage reactions in the benzenes of TPhT occurred individually and synchronously, producing diphenyltin, monophenyltin and tin accordingly.

[Characteristic and ion exchanges during Cu2+ and Cd2+ biosorption by Stenotrophomonas maltophilia].

The characteristics of Cu2+ and Cd2+ biosorption by Stenotrophomonas maltophilia (S. maltophilia) under different biomass, metal concentration and glutaraldehyde content were studied and the correlations among metal biosorption, NO3- removal and ion release were analyzed. The mechanism was explored through ion biosorption, exchange, conversion and release. The experimental results demonstrated that S. maltophilia was an efficient strain to remove Cu2+ and Cd2+. The biosorption efficiencies of Cu2+ and Cd2+ achieved 96.3% and 83.9%, respectively after dealing with 0.05 mmol x L(-1) aqueous solutions for 120 min with dry biosorbent dosage of 0.2 g x L(-1). Cu2+ and Cd2+ biosorption by S. maltophilia included surface adsorption, transmembrane active transportation, bioaccumulation of NO3- and reduction of NO3- to NO2-. The intracellular transfer and reduction of NO3- to NO2- during biosorption by S. maltophilia were energy-consuming biological processes. It could also promote the release of Cl-, PO4(3-), SO-4(2-), Na+, NH4+, K+ and Ca2+. From FTIR investigation, involvement of various functional groups like acetylamino, hydroxyl and carboxyl in the binding of Cu2+ and Cd2+ was evident. Moreover, XPS results proved that the valence state of Cu2+ and Cd2+ did not changed by biosorption.