The vertical distribution of 35 volatile organic compounds (VOCs) was investigated in soil columns from two obsolete industrial sites in Eastern China. The total concentrations of ΣVOCs in surface soils (0-20 cm) were 134-1664 ng g-1. Contamination of VOCs in surface soil exhibited remarkable variability, closely related to previous production activities at the sampling sites. Additionally, the concentrations of ΣVOCs varied with increasing soil depth from 0 to 10 m. Soils at depth of 2 m showed ΣVOCs concentrations of 127-47,389 ng g-1. Among the studied VOCs, xylene was the predominant contaminant in subsoils (2 m), with concentrations ranging from n.d. to 45,400 ng g-1. Chlorinated alkanes and olefins demonstrated a greater downward migration ability compared to monoaromatic hydrocarbons, likely due to their lower hydrophobicity. As a result, this vertical distribution of VOCs led to a high ecological risk in both the surface and deep soil. Notably, the risk quotient (RQ) of xylene in subsoil (2 m, RQ up to 319) was much higher than that in surface soil. Furthermore, distinct effects of VOCs on soil microbes were observed under aerobic and anaerobic conditions. Specifically, after the 30-d incubation of xylene-contaminated soil, Ilumatobacter was enriched under aerobic condition, whereas Anaerolineaceae was enriched under anaerobic condition. Moreover, xylene contamination significantly affected methylotrophy and methanol oxidation functions for aerobic soil (t-test, p < 0.05). However, aromatic compound degradation and ammonification were significantly enhanced by xylene in anaerobic soil (t-test, p < 0.05). These findings suggest that specific VOC compound has distinct microbial ecological effects under different oxygen content conditions in soil. Therefore, when conducting soil risk assessments of VOCs, it is crucial to consider their ecological effects at different soil depths.

Xylene exposure is known to induce toxicity in hematopoietic stem and progenitor cells (HSPCs), leading to bone marrow suppression and potential leukemogenesis. However, research on the gene expression profiles associated with xylene-induced toxicity in HSPCs, and effective therapeutic interventions, remains scarce. In our study, we employed single-cell RNA sequencing to capture the transcriptomic shifts within bone marrow HSPCs both prior to and following treatment with coniferyl ferulate (CF) in a mouse model of xylene-induced hematotoxicity. Subsequently, we pinpointed CF as a targeted agent using SPR-LC/MS analysis. This enabled us to confirm the link between the gene Mgst2 and specific cellular subtypes. Our data revealed that CF significantly countered the reduction of both monocyte and neutrophil progenitor cells, which are commonly affected by xylene toxicity. Through targeted analysis, we identified Mgst2 as a direct molecular target of CF. Notably, Mgst2 is preferentially expressed in neutrophil progenitor cells and is implicated in mitochondrial metabolic processes. By selectively inhibiting Mgst2 in bone marrow, we observed amelioration of xylene-induced hematotoxic effects. In summary, our findings suggest that coniferyl ferulate can mitigate the detrimental impact of xylene on hematopoietic stem and progenitor cells by targeting Mgst2, particularly within subpopulations of neutrophil progenitors. This discovery not only advances our comprehension of the cellular response of HSPCs to xenobiotic stressors like xylene but also identifies CF and Mgst2 as potential therapeutic targets for alleviating xylene-induced hematotoxicity.

This work presents the first example of the utilization of polar ester group functionalized pillar[6]arene (P6A-C10-OAc) as a stationary phase for capillary gas chromatographic (GC) separations. The statically coated P6A-C10-OAc column showed a high column efficiency of 5393 plates/m and moderate polar nature. Its resolving capability and retention behaviors were investigated for a mixture of 20 analytes and more than a dozen isomers from apolar to polar in nature. As evidenced, the P6A-C10-OAc column achieved high-resolution separations of all the analytes and good inertness. Importantly, it exhibited distinctly advantageous performance for high resolution of the challenging isomers of xylenes, diethylbenzenes, ethyltoluenes, and halobenzenes over the commercial HP-5 (5% phenyl dimethyl polysiloxane), HP-35 (25% phenyl dimethyl polysiloxane), and PEG-20M (polyethylene glycol) columns.

In this work, a series of clinoptilolite composites decorated with carbon quantum dots (CQDs/clinoptilolite) with hierarchical pore structures was demonstrated that exhibits good photocatalytic performance for the removal of xylene. The technique for the attachment of carbon quantum dots to clinoptilolite was prepared by a hydrothermal method in this study. The structural features were confirmed by SEM, TEM, EDS, XRD, BET, XPS, and solid diffuse reflection measurements, while the degradation mechanism was investigated by adding a trapping agent into the nanocomposites. The introduction of CQDs promoted the separation of photogenerated electrons and holes as well as the generation of reactive radicals, which effectively improved the light utilization and even increased the degradation rate of xylene by 73% at the optimal state. The photocatalytic test was conducted under a different dwell time, catalyst dosage, initial concentration, and illumination intensity. The results showed that the degradation rate of xylene by the CQDs/clinoptilolite catalyst reached 97.4% under the optimal reaction conditions (the catalyst was Catalyst No. 2, the residence time was 90 s, the initial concentration was 2.5 g/m3, the light intensity was three lamps for irradiation, and the catalyst dosage was 0.05 g). In addition, the degradation efficiency of the CQDs/clinoptilolite photocatalyst still reached 78% after eight consecutive catalytic regeneration cycles. This work sheds new light on the degradation of xylene.

Xylene has the potential to cause nervous system disturbances since it is a lipophilic substance with high affinity for lipid-rich tissue, such as the brain. Involvement in the spinal cord, especially long segmental spinal cord lesions that permeate almost the entire cervical and thoracic spinal cord, is extremely rare. We report two cases of occupational exposure to excessive xylene, both of which presented with severe and rapidly progressive numbness and weakness in the limbs that, more importantly, led to poor outcomes: one died and the other was left severely disabled. In both, spinal magnetic resonance imaging showed long segmental lesions in the cervicothoracic spinal cord. These findings may provide some insights into the effects of xylene as an isolated agent on the spinal cord injury.

With the development of the chemical industry, benzene, toluene, ethylbenzene, and xylene (BTEX) have gradually become the major indoor air pollutants. Various gas treatment techniques are widely used to prevent the physical and mental health hazards of BTEX in semi-enclosed spaces. Chlorine dioxide (ClO2) is an alternative to chlorine as a secondary disinfectant with a strong oxidation ability, a wide range of action, and no carcinogenic effects. In addition, ClO2 has a unique permeability which allows it to eliminate volatile contaminants from the source. However, little attention has been paid to the removal of BTEX by ClO2, due to the difficulty of removing BTEX in semi-enclosed areas and the lack of testing methods for the reaction intermediates. Therefore, this study explored the performance of ClO2 advanced oxidation technology on both liquid and gaseous benzene, toluene, o-xylene, and m-xylene. The results showed that ClO2 was efficient in the removal of BTEX. The byproducts were detected by gas chromatography-mass spectrometry (GC-MS) and the reaction mechanism was speculated using the ab initio molecular orbital calculations method. The results demonstrated that ClO2 could remove the BTEX from the water and the air without causing secondary pollution.

Advancing the practical application of catalytic oxidation technology demands for illustrating the synchronous conversion behavior of various volatile organic compounds (VOCs) over catalysts. Here, the mutual effects of benzene, toluene and xylene (BTX) were examined for their synchronous conversion on the surface of the MnO2 nanowire. Competitive adsorption of xylene (absorption energy (Eads): -0.889 eV) facilitated its prior conversion and impeded the oxidization of toluene and benzene over the catalyst. The turnover frequencies were 0.52 min-1 (benzene), 0.90 min-1 (toluene) and 2.42 min-1 (xylene) for mixed BTX conversion over the MnO2. Doping MnO2 with K+, Na+ and Ca2+ could enhance its ability to oxidize the individual VOCs but did not alter the conversion mechanism of mixed BTX over the catalyst. When reducing the competitive effects in the adsorption of BTX, the oxidation performance of catalysts would depend on their ability to oxidize toluene and benzene. K-MnO2 showed superior properties, i.e. specific surface area, highly low-valent Mn species, high lattice oxygen content, and abundant oxygen vacancy, and then exhibited superior performance during long-term operation (90% conversion in 800 min). The present study uncovered the co-conversion mechanism of multiple VOCs and significantly leveraged the catalytic oxidization technology for VOCs removal in practical application.

This article reports a poisoning case after occupational exposure to toluene, xylene, and ethylbenzene for 3 days. The main clinical manifestation of the patient was consciousness disorder. After dehydration, cerebral awakening, anti-epileptic and anti-myoclonic treatment, the patient had secondary epilepsy and cerebellar ataxia for a long time. According to diagnostic criteria, the patient was diagnosed with occupational acute chemical poisoning (severe) , occupational acute chemical poisoning sequelae. It is suggested that the clinical awareness of benzene compound poisoning should be strengthened, early diagnosis and early treatment should be carried out to improve the prognosis of patients.
本文报道1例职业性接触甲苯、二甲苯、乙苯3 d后中毒病例。患者以意识障碍为主要临床表现，经脱水、醒脑、抗癫痫及抗肌阵挛等治疗后，长期遗留有继发性癫痫及小脑共济失调。根据标准诊断患者为职业性急性化学物中毒（重度）、职业性急性化学物中毒后遗症。提示临床应加强对苯类化合物中毒的认识，早诊断、早治疗，以改善患者预后。.

Aiming at the problems of high xylene concentration and difficult removal in heavily polluted areas, high-efficient degrading bacteria of volatile organic compounds (VOCs) xylene in heavily polluted areas were selected and screened from sewage sludge, and their degradation characteristics were studied. The response surface methodology (RSM) optimized the optimal degradation conditions. The results showed that the screened degrading strain was identified as Klebsiella by the 16SrDNA technology and named H-16. During the start-up phase of the reactor, the removal rate of xylene by strain H-16 fluctuated, and it was stable above 71.3% for 150 min. At 40°C, the degradation rate is the highest, reaching 63.25%. With an increasing inoculum amount of strain H-16, the degradation rate of xylene gradually increased, and the degradation rate could reach 86.1% when the inoculation amount was 25%. A neutral environment was more conducive to the degradation and removal of xylene. Through the analysis of the model and RSM, the optimal conditions for the degradation of xylene by H-16 were obtained: 38.89°C, pH 6.94 and 18.07%. GC-MS results showed that the possible degradation pathway of xylene began with demethylation, formation of pentene diacid by benzene ring cleavage, and finally oxidation to generate CO2 and H2O.

CuO/WO3 hierarchical hollow microspheres, assembled from irregular two dimensional (2D) nanosheets, were prepared by ultrasonic-wet chemical etching and pyrolysis in this study. The sensing performance of Micro-Electro-Mechanical System (MEMS) xylene gas sensor based on CuO/WO3 hierarchical structure were evaluated. It was found that the CuO/WO3 MEMS sensors showed an enhanced gas sensing performance compared with pristine WO3 sensor. The CuO/WO3-3 (the mass ratio of CuO to WO3 is 3%) sensor exhibited faster response-recover speed and the highest response value to xylene. Moreover, the CuO/WO3-3 sensor possessed higher selectivity and long-term stability. The good sensing properties can be attributed to the unique three dimensional (3D) hierarchical structure and p-n heterojunction of CuO-WO3. Considering the above advantages, the CuO/WO3-3 sensor has a great potential for the rapid detection and monitoring of xylene.