Surface chemistry of tribochemical reactions explored in ultrahigh vacuum conditions

The thermal decomposition of model extreme-pressure lubricant additives on clean iron was studied in ultrahigh vacuum conditions using molecular beam strategies. Methylene chloride and chloroform react to deposit a solid film consisting of FeCl₂ and carbon, and evolve only hydrogen into the gas phase. No gas-phase products and less carbon on the surface are detected in the case of carbon tetrachloride. Dimethyl and diethyl disulfide react on clean iron to deposit a saturated sulfur plus carbon layer at low temperatures (∼600 K) and an iron sulfide film onto a Fe + C underlayer at higher temperatures (∼950 K). Methane is the only gas-phase product when dimethyl disulfide reacts with iron. Ethylene and hydrogen are detected when diethyl disulfide is used.     

Enzymatic degradation of esters of dichloropropanols: removal of chlorinated glycerides from processed foods

The esters of dichloropropanols from the byproduct of hydrolysates during food processing were degraded by the cell-free extracts of a dichloropropanol-assimilating bacterium of Pseudomonas sp. OS-K-29. 1-Acyloxy-2,3-dichloropropane was hydrolysed into the corresponding carbonic acid and 2,3-dichloropropanol, and then the dichloropropanol was dechlorinated. The esterase activity of the cell-free extracts was effective for the esters of the dichloropropanols and monoacylglycerides, but not for hydrolysing the lipase substrates such as triacylglycerides and Tween 60. A comparative study using a series of octanoyl glycerides and the esters of the dichlopropanols showed that the substrate specificities of the cell-free extracts were similar to the monoacylglyceride lipase from Penicillium camembertii.     

Electrochemical pre-treatment of effluents containing chlorinated compounds using an adsorbent

Electrochemical pre-treatment of industrial wastewater to remove refractory and/or toxic organic components, making them more amenable to biological treatment, is likely to be more cost-effective than using a physical or chemical process for complete organic removal. This paper demonstrates the use of a carbon-based adsorbent material that preferentially removes chlorinated organic compounds. Electrochemical regeneration of the adsorbent is shown to be a quick, easy and cheap process, because the adsorbent is both highly electrically conducting and non-porous. High regeneration rates over a number of cycles were obtained by passing a charge of 25 C g⁻¹ through a bed of adsorbent particles, at a current density of 20 mA cm⁻² for 10 min. The energy required to remove a kg of COD from an industrial wastewater was calculated to be 27 kWh.     

PHASE EQUILIBRIUM FOR TERNARY LIQUID SYSTEMS OF WATER CARBOXYLIC ACID CHLORINATED HYDROCARBON: THERMODYNAMIC MODELING THROUGH SERLAS

Liquid-liquid equilibrium data of the solubility (binodal) curves and tie-line end compositions are presented for mixtures of [water (1) + formic acid, or acetic acid, or propanoic acid (2) + chlorobenzene, or 1,2-dichloroethane (3)] at T = 293.2 K and P = 101.3 ± 0.7 kPa. A log-basis approach, SERLAS (solvation energy relation for liquid-associated system), has been proposed to estimate the properties and liquid-liquid equilibrium (LLE) of associated systems containing proton-donating and -accepting and polar components capable of a physical interaction through hydrogen bonding or dipole-dipole interaction. The tie lines were also correlated using the UNIFAC-original model. The reliability of the models has been analyzed against the LLE data with respect to the distribution coefficient and separation factor. The proposed model appears to be an improvement in data fit for the ternary systems, yielding a mean relative error of 10.1% for all the systems considered.     

氯化聚乙烯接枝马来酸酐胶粘剂的研究

本文介绍了改性聚丙烯（PP）基泡沫材料用的水溶性胶粘剂的研制。该胶粘剂不影响泡沫材料的阻燃性能和吸声性能，并有较好的热稳定性和储存性以及优化的耐水性。     

"胶乳法"氯化天然橡胶薄层干燥影响因素的研究

采用二次回归正交设计方法,对“胶乳法“氯化天然橡胶(CNR)进行薄层干燥试验.分析了热风温度、风速和物料的粒径等因素对干燥速率、干燥后物料性能的影响规律,确定了影响物料薄层干燥速率各因素的主次,提出了较佳的干燥工艺和合理的性能参数.     

Long-term performance of a HDPE geomembrane stabilized with HALS in chlorinated water

A high density polyethylene geomembrane (GMB) stabilized with hindered amine (light) stabilizers (HALS or HAS) is immersed in four chlorinated water solutions with a simulated free chlorine concentration range of 0.5–5 ppm at five different temperatures (25, 40, 65, 75, and 85 °C) for 70 months. Standard and high pressure oxidative induction time (OIT) tests are performed to monitor antioxidants depletion while melt flow index, tensile, and stress crack resistance (SCR) tests are conducted to monitor degradation in physical and mechanical properties. Degradation in the GMB properties occurred shortly after immersion in chlorinated water at all temperatures except at 25 °C. Increasing the free chlorine concentration resulted in faster degradation of the tensile properties and SCR. The predicted time to nominal failure based on SCR ranges between 25 years at 40 °C and 5 years at 85 °C in chlorinated water (with 0.5 ppm free chlorine). A comparison between the degradation in SCR of this GMB and a GMB with a different resin and without HALS shows significant difference in their performance in chlorinated water but not in other incubation media.     

Treatment of Groundwater Contaminated with 1,4-Dioxane,Tetrahydrofuran, and Chlorinated Volatile Organic Compounds Using Advanced Oxidation Processes

Ozonation and four types of advanced oxidation processes, including O₃/H₂O₂, O₃/UV, O₃/H₂O₂/UV, and UV/H₂O₂, were evaluated for the treatment of contaminated groundwater at a Superfund site in Simpsonville, South Carolina using bench-scale, batch ozone and UV apparatuses. Although the contaminants of concern were 1,4-dioxane, 1,1-dichloroethene, and trichloroethene, several other chlorinated organics as well as tetrahydrofuran were found in the groundwater samples. The O₃/H₂O₂ treatment with O₃ and H₂O₂ doses of 6 and 1.5 mg/L, respectively, and the UV/H₂O₂ treatment with UV and H₂O₂ doses of 1,000 mJ/cm and 20 mg/L, respectively, were sufficient to degrade 200 µg/L of 1,4-dioxane, 110 µg/L of 1,1-dichloroethene, and 10 µg/L of trichloroethene below their performance standards of 10, 7, and 4 µg/L, respectively. Due to a high bromide concentration (0.35 mg/L) in the groundwater sample, bromate formation was found to be significant in ozone-based treatment, including O₃/H₂O₂.     

Environmentally friendly phthalocyanine catalysts for water decontamination—Non-photocatalytic systems

Macrocyclic porphyrin-like compounds known as phthalocyanines (Pcs) have been shown to produce singlet oxygen species upon illumination with light of an appropriate wavelength. Singlet oxygen is an effective agent for complete oxidation of common water-soluble pollutants including chlorinated phenols. The most active are, in this respect, phthalocyanines bearing Al, Zn and Si central atoms. Although these compounds were proofed to be virtually non-toxic, the presence of the Al³⁺ and Zn²⁺ ions may contradict this. On the other hand e.g. iron phthalocyanine (FePc) does not represent any danger from this point of view. However, due to the specific coordination of its central metal ion and also because of the number of electrons occupying its valence orbitals, the FePc cannot be effectively activated by the photon flux. Here we report on an alternative system in the dark. It is based on the initial catalytic decomposition of various peroxo substances by metal Pc, producing oxidising species which can decompose chlorinated phenols. A series of Pcs and peroxo substances were compared and the reaction system optimised. It was shown that the highest activity was revealed for the system comprising of FePc and tert-butylhydroperoxide. Iron phthalocyanine was also successfully immobilised on an Al₂O₃ solid matrix, and this heterogeneous system was tested analogously to the homogeneous one. Virtually zero leaching of the anchored complex was detected and the activity was found to be comfortably high.