Recovery efficiency of the hydrofluorocarbon (HFC‐134a) by activated carbons of different physicochemical properties

The adsorption characteristics of 1,1,1,2‐tetrafluoroethane (HFC‐134a) on activated carbon were investigated to evaluate the recovery efficiency of HFC‐134a by six activated carbons (two granular activated carbons (GAC1 and GAC2), one high‐surface area activated carbon (HAC), and three activated carbon fibers (ACF10, ACF15, and ACF20)). HFC‐134a adsorption on the activated carbons increased with increase in the specific surface area and pore volume of the activated carbon. The differential heat of the HFC‐134a adsorption decreased with increase in the percentage of the micropore volume to the total pore volume. The adsorption model of HFC‐134a on the activated carbon could be based on the Langmuir model. The constant a of the Langmuir plot of HAC and ACF20 is smaller than GAC1 or GAC2 and ACF10 or ACF15, respectively. The constant W_s of HAC has the largest value. The constant a was correlated to the heat of adsorption. It is concluded that the largest amount of HFC‐134a was adsorbed on HAC, and the least amount of interaction occurred between HFC‐134a and the HAC. The amount of HFC‐134a adsorbed on the activated carbons over time was applied to the Sameshima equation. The adsorption rate constant of HFC‐134a on HAC was the largest. The HAC could be suitable for the recovery of HFC‐134a.     

Treatment of dye‐containing wastewater by sequencing batch reactor with powdered activated carbon addition

The process involving the combination of powdered activated carbon (PAC) and biomass in the aeration basin of conventional continuous‐flow activated sludge system, known as the PACT process, has proven to be effective for treating toxic pollutants present in industrial wastewaters. In view of the many advantages of sequencing batch reactors (SBR) operationally, the objective of this study is to evaluate the PACT process under SBR operation to treat wastewater containing Acid Blue 25 (AR) and Basic Yellow 2 dyes (BR). The SBR systems were operated with FILL, REACT, SETTLE and DRAW periods in the ratio of 0.25:3.75: 1.0:1.0 for a cycle time of 6 h. The average COD and AR removal efficiencies were 89% and 93%, respectively with PAC addition compared to 76% and 7%, respectively, without PAC addition. In the case of BR, the average removal efficiencies of COD and dye increased from 52% and 9% to 90% and 93%, respectively, with PAC addition. Kinetic study conducted for the REACT period showed that both dyes exhibited a very pronounced inhibitory effect on the activities of the microorganisms. The addition of PAC was capable of reducing the inhibitory effect of only BR but not AR on the microorganisms.     

Transport of butyltins at the water‐air interface and the adsorptive behavior of tributyltin in the surface microlayer

The transfer dynamics and enrichment phenomena of monobutyltin chloride(MBT), dibutyltin chloride(DBT) and tributyltin chloride(TBT) at the water‐surface microlayer (SM) interface were studied. The transport processes of the three compounds at the interface are very fast in the estuarine environment. The mass transfer coefficients are 1.54 m/h for MBT, 2.16 m/h for DBT, 1.56 m/h for TBT. The effect of various factors, including pH, salinity, suspended particulate and temperature, on the adsorptive behavior of TBT in the water's surface microlayer was also studied.     

Effects of the Ellagic acid on the N‐Acetyltransferase activity and Acetylation of 2‐aminofluorene in the rat

The effects of the ellagic acid on the in vitro and in vivo acetylation of 2‐aminofluorene were investigated in male Sprague‐Dawley rats. For in vitro examination, cytosols with or without ellagic acid co‐treatment showed different percentage of 2‐aminofluorene acetylation. For in vivo examination, pre‐treatment of male rats with ellagic acid (10 mg/kg) 24h prior to the administration of 2‐aminofluorene (50 mg/kg) resulted in a 26% and 29%, respectively, decrease in the urinary and fecal recovery of N‐acetyl‐2‐aminofluorene, and a 37% decrease in the metabolic clearance of 2‐aminofluorene to N‐acetyl‐2‐aminofluorene. This is the first demonstration that ellagic acid decrease the N‐acetylation of carcinogens in vitro and in vivo.     

Worldwide effects of non-native species on species–area relationships

Non-native species have invaded most parts of the world, and the invasion process is expected to continue and accelerate. Because many invading non-native species are likely to become permanent inhabitants, future consideration of species-area relationships (SARs) should account for non-native species, either separately or jointly with native species. If non-native species occupy unused niches and space in invaded areas and extinction rate of native species remains low (especially for plants), the resultant SARs (with both native and non-native species) will likely be stronger. We used published and newly compiled data (35 data sets worldwide) to examine how species invasions affect SARs across selected taxonomic groups and diverse ecosystems around the world. We first examined the SARs for native, non-native, and all species. We then investigated with linear regression analyses and paired or unpaired t tests how degree of invasion (proportion of non-native species) affected postinvasion SARs. Postinvasion SARs for all species (native plus non-native) became significantly stronger as degree of invasion increased (r² = 0.31, p = 0.0006), thus, reshaping SARs worldwide. Overall, native species still showed stronger and less variable SARs. Also, slopes for native species were steeper than for non-native species (0.298 vs. 0.153). There were some differences among non-native taxonomic groups in filling new niches (especially for birds) and between islands and mainland ecosystems. We also found evidence that invasions may increase equilibrial diversity. Study of such changing species–area curves may help determine the probability of future invasions and have practical implications for conservation.     

Synthesis and antithyroid activity of 6‐n‐propyl‐5‐arylazo‐2‐thiouracils †

The synthesis of several 6‐n‐propyl‐5‐arylazo‐2‐thiouracil derivatives was achieved. The antithyroid activity of these derivatives has been determined using iodine‐125‐thiocyanate discharge technique in rats, and 6‐n‐propyl‐2‐thiouracil (PTU) as a standard. None of the 5‐arylazo‐2‐thiouracil analogs showed antithyroid activity as compared to PTU. The structure‐activity relationships (SAR) of position 5 in the PTU molecule and the requirements for better binding to the proposed receptor are discussed.     

Photochemical reaction of peroxynitrite and carbon dioxide could account for up to 15 % of carbonate radicals generation in surface waters

The carbonate radical (CO ₃ ^?· ) is a photoinduced transient species occurring in surface waters. The carbonate radical can transform both natural compounds and xenobiotics. For instance, it can react with electron-rich substrates such as anilines, phenols and organic sulfur compounds. Here we used the APEX software to assess photochemical reactions, including the formation rates of transient species, based on water chemistry and depth, under summertime irradiation conditions. We found that the reaction between peroxynitrite and carbon dioxide is a potentially significant source of CO ₃ ^?· in sunlit surface waters, and could account for up to 10–15 % of the total CO ₃ ^?· formation. The peroxynitrite pathway to CO ₃ ^?· would be most significant at pH 7–8 and would be enhanced in waters with elevated nitrate and low alkalinity. Therefore, the proposed process could add to the known photochemical sources of CO ₃ ^?· in surface-water environments.     

Effects of warming on leaf non-structural carbohydrates and carbon and nitrogen isotopes of Cunninghamia lanceolata saplings during different seasons北大核心CSCD

To reveal the response of non-structural carbohydrates (NSC) and carbon and nitrogen isotopes in plant leaves to global warming, we conducted soil warming experiments in the Fujian Sanming Forest Ecosystem and Global Change National Observation and Research Station of China. We designed two treatments: control (CT) and warming (W; cable heating, +4 ℃). Heating cables were installed 20 cm from each other at a depth of 10 cm and were heated in March 2016. In this study, Cunninghamia lanceolata saplings were used to analyze seasonal changes in leaf non-structural carbohydrates, and carbon and nitrogen isotopes. The results showed that (1) warming significantly reduced the soluble sugar, starch, and NSC content of leaves in spring but without any significant difference during other seasons. (2) Leaf δ13C increased significantly in spring and winter after warming, whereas leaf δ15N did not change significantly. (3) No significant correlation was observed between leaf δ13C, δ15N, or NSC content during the warming treatment, but a negative correlation was observed between leaf δ15N, δ13C, and sugar to starch ratio. A positive correlation between leaf δ15N and starch content was identified. In summary, when temperature increases, plants adjust the NSC content during different seasons for osmotic regulation, change the characteristics of the nutrient cycle, and alter the plant water and nutrient use strategies to maintain plant growth. In the future, we should further study the seasonal variation characteristics of NSC content and isotopes and the relationship between NSC content and the carbon and nitrogen cycles in plants under the context of long-term warming. © 2022 Science Press. All rights reserved.     

Generation of new carbon–carbon and carbon–heteroatom bonds mediated by agro-waste extracts: a review

Agro-waste extracts are considered green solvents since they are easy to handle, readily accessible from natural waste feedstock, biodegradable and recyclable. Therefore, the employment of these extracts in reaction media has emerged as the most useful and eco-friendly alternative in modern organic chemistry. Here, we review recent developments for the generation of new carbon–carbon and carbon–heteroatom bonds mediated by agro-waste extracts. We show that these aqueous extracts have great applicability in several transformations, including condensations, oxidations, multicomponent and coupling reactions. The challenges and advantages on the use of water of agro-waste extracts in synthetic methodologies is also detail.

     

Concentrations of polychlorinated dibenzo‐p‐dioxins and dibenzofurans in outdoor air of North‐Rhine‐Westphalia,Germany

Measurements of polychlorinated dibenzo‐p‐dioxins (PCDD) and dibenzofurans (PCDF) in outdoor air of North‐Rhine‐Westphalia were carried out. Fifty‐six samples were taken at different sites in areas of different land use and emission structures. A special filter system allowed analysis of the gas and particle phases separately. It was found that higher chlorinated PCDD/PCDF (7 or 8 chlorine atoms) are collected on glass fiber filter and lower chlorinated PCDD/PCDF (tetra‐ and penta‐CDD/CDF) are absorbed on polyurethane foam. The following isomers were determined: OCDD, OCDF and 11 isomers with chlorine substitution in 2,3,7,8‐position as well as the sum of TCDD, PeCDD, HxCDD, HpCDD, TCDF, PeCDF, HxCDF, HpCDF and the sum of PCDD (4–8) and PCDF (4–8). No 2,3,7,8‐TCDD could be detected but 2,3,7,8‐TCDF was found at 15 sites. Mean concentration in the Rhine‐Ruhr‐District for the sum of PCDD (4–8) and PCDF (4–8) was 3.2pg/m³ and 5.5pg/m³ respectively. Detection limit for TCDD and PCDD/PCDF (5–8) was 0.1–0.2 pg/m³ and 0.005–0.015 pg/m³ respectively. There is no significant indication that 2,3,7,8‐chlorinated isomers of PCDD/PCDF are predominantly decomposed by photochemical reactions in outdoor air.     

Genotoxicity evaluation of surface waters located in urban area of Xi’an City using Vicia faba bioassays

In this study, micronucleus （MCN） and chromosome aberration （CA） tests in Vicia faba root tip cells were carried out in order to assess the water quality and the comprehensive genotoxic potential of surface waters located in the urban area of Xi＇an City, China. For these evaluations, water samples from different surface waters （four rivers, two lakes, two biological treatment plant effluents） were collected, the ultra-pure water and methyl methanesulfonate solution was used as the negative and positive control, respectively. In our results, highly significant differences in MCN perrnillage （average number of micronuclei per 1000 cells）, CA frequencies and PI （pollution index） values were found among three rivers and two WWTP effluents, the tested samples from two rivers caused the decrease of mitotic index over 22% compared with the negative control. No significant changes were observed in micronuclei and chromosome aberrations frequencies at one river and two lakes during the period of test （wet season）. These results point out a poor state of the water quality and genotoxic activity of the main surface waters in Xi＇an City. It is recommended to establish a monitoring program for the presence of genotoxic agents in these surface waters.     

Effects of cucl2 on UV‐mutagenesis and on DNA damage in a restriction fragment of E. Coli gpt∗

CuCl₂ does not cause Trp⁺ reversion in E. coli WP2. However, when the bacteria are exposed to CuCl₂ and UV‐irradiated, a greater than 3‐fold enhancement of mutagenesis (compared to UV alone) is seen at 30 μMCuCl₂, and significant enhancement is seen even at 3 μM. The mechanism for this comutagenic effect was studied using a restriction fragment of the E. coli gpt gene. Whereas UV or CuCl₂ alone caused few strand breaks, UV + CuCl₂ induced breaks at every site. This reaction was blocked by KI, a free radical scavenger. While UV alone induced alkali‐labile sites, UV+ CuCl₂ induced many more such sites and altered the sequence specificity. We suggest that at least some of the comutagenic effect might be due to hydroxyl radical formed via a Fenton reaction.     

Cross‐sectional epidemiological study on the lead burden of children and workers in Greece

Exposure of the general population to lead in the environment is mainly caused by motor traffic exhaust and by industrial pollution. The aim of the study in Greece was to assess lead exposure in children living in point source impacted areas (Lavrion and Aspropyrgos‐Eleusis) using the biological monitoring parameter “blood lead concentration”;.

In addition, workers of a lead smelter, a battery plant and an oil refinery were investigated in these areas at the same time.

Five hundred and thirty‐four children and 105 workers took part in this investigation.

The highest blood lead levels (mean: 24.16 μg/100ml; range: 10.40–60.49 μg/100 ml) were found in children living in a 500m‐area around the lead smelter at Lavrion. Blood lead decreases corresponded to the increasing distance from the emitter. Nevertheless the values of children living in a 1500 m distance to the smelter are significantly higher than those of children living next to other kinds of industrial lead sources.

The mean values of the children living in the two industrial towns were manifold higher than those of the control group.

The blood lead levels of the investigated workers did not exceed the German BAT‐value (Biologischer Arbeitsstoff‐Toleranzwert) of 70 μg/100ml.     

Removal of Cu（ll） ions from aqueous solution by activated carbon impregnated with humic acid

Humic acid （HA） was impregnated onto powdered activated carbon to improve its Cu（II） adsorption capability. The optimum pH value for Cu（II） removal was 6. The maximum adsorption capacity of HAimpregnated activated carbon was up to 5.98mg.g-1, which is five times the capacity of virgin activated carbon. The adsorption processes were rapid and accompanied by changes in pH. In using a linear method, it was determined that the equilibrium experimental data were better represented by the Langmuir isotherm than by the Freundlich isotherm. Surface charges and surface functional groups were studied through zeta potential and FTIR measurements to explain the mechanism behind the humicacid modification that enhanced the Cu（II） adsorption capacity of activated carbon.     

Impacts of inter-sectoral trade on carbon emissions—a case of China in 2007

With the increase in international trade, more attention has been given to quantifying the impacts of international trade on energy use and carbon emissions. Input-output analysis is a suitable tool for assessing resources or pollutants embodied in trade and it has become a critical tool for performing such analysis. This study estimated the national and sectoral carbon emissions embodied in Chinese international trade using the latest available China input-output table of 2007. The results showed that a significant exporting behavior of embodied carbon emissions existed in China??s trade. Over 1/3 of the emissions in Chinese domestic production processes were generated for exports in 2007. The net balance of emissions embodied in exports and imports accounted for nearly 30% of China??s domestic emissions, which means that any policy made to increase the exports would result in a significant growth of China??s domestic emissions. Since over half of China??s export trade is processing trade, the re-exported emissions could not be overlooked; otherwise, it would hard to capture the actual emissions generated abroad to obtain China??s domestic consumption. The enlargement of export scale is a primary driven factor to the rapid growth of China??s exported emissions. It is necessary for China to adjust its economic and industrial structure to reduce the dependence of economic growth on the export trade. However, when adjusting industry structures or making policies on carbon emission reduction, it will be more reasonable to consider the relationship between production and consumption, rather than just focus on the emission values of sectors?? direct production, as a large part of carbon emissions emitted by the principal direct polluters were generated to obtain the products which were required by other sectors.     

Effects of lead and selected pyrethroids/piperonyl butoxide alone and in combination on Na,K‐ATPase

In vitro effects of Pb²⁺, the pyrethroid insecticides cypermethrin, fenvalerate and the syner‐gist piperonyl butoxide on sodium‐potassium‐activated adenosine triphosphatase (Na,K‐ATPase) from dog kidney were determined. Pb²⁺ with an estimated IC50 value of 5.2 μM was found to be a potent inhibitor of Na,K‐ATPase activity, whereas Na,K‐ATPase was less sensitive to the pyrethroids tested and piperonyl butoxide. Investigation with circular dichroism (CD) spec‐troscopy showed that inhibition occurs through conformational changes of the α‐subunit of the enzyme. The kinetic characteristics of inhibition of Na,K‐ATPase with varying substrate (ATP) concentrations as well as with varying Na⁺ concentrations exhibited a competitive type of inhibition with Pb²⁺ in the μM range. With Pb²⁺ alone in the enzyme assay no conformational changes of the protein could be observed which confirmed the assumption that Pb²⁺ can bind to the Na⁺ binding site of the α‐subunit. Uncompetitive type of inhibition occurred with varied K⁺ concentrations demonstrating that this cation binding site is not affected directly by Pb²⁺.

Complete reversal of Pb²⁺ by DTT confirms that a possible target for interaction of this heavy metal ion with Na, K‐ATPase are specific SH groups.

Synergistic effects could only be determined with higher Pb²⁺ concentrations of 3, 5 and 7 μM plus piperonyl butoxide while all other combinations with this heavy metal plus organic substances where of the additive type. With CD spectroscopy also only additive effects were observed. These results demonstrate that higher concentrations of piperonyl butoxide favor the binding of Pb²⁺ to the Na⁺ binding site by conformational changes of the protein.     

Cross‐sectional epidemiological study on arsenic excretion in urine of children and workers in Greece

An investigation was undertaken to study the exposure of children in areas with different air pollution and of adults working in three different plants (lead processing, battery plant, oil refinery) using arsenic in urine as a biological parameter. The arsenic excretion of the children are in agreement with the air pollution in the investigated areas. The workers in the lead processing plant are found to have the highest urine excretion values of the three worker collectives. The mean excretion values is nearly ten times higher than that found in the normal population.     

Study on polychlorinated dibenzo‐p‐dioxins and dibenzofurans in rivers and estuaries in Osaka Bay in Japan

In order to search the source of polychlorinated dibenzo‐p‐dioxins (PCDDs) and dibenzofurans (PCDFs) in blue mussel in Osaka bay, sediments from Osaka bay and from rivers running near an urban municipal incinerator were analysed for PCDDs, PCDFs and PCBs. The river and estuary sediments were all found to be contaminated with PCDDs at average levels of 9.8 and 12ppb on the dry basis, PCDFs of 7.8 and 5.1 ppb, and PCBs of 1600 and 1300ppb, respectively. The two sediments contained similar profiles of specific isomers and congeners of PCDDs and PCDFs with each other. In addition, there was observed positive close correlations between PCDD and PCDF levels in the two specimens as well as fly ash from urban municipal incinerators. These allow the conclusion that the main source of the two chemicals in Osaka bay is fly ash from waste incineration.     

Alkylation of metals and the activity of metal‐alkyls†

The biochemical basis for resistance to metal ion toxicity is emerging though it is complicated by the different resistance mechanisms. Several strategies for resistance to toxic metal ions have been identified:

1. The development of energy driven efflux pumps which keep toxic element levels low in the interior of the cell. Such mechanisms have been described for Cd(II) and As(V).

2. Oxidation (e.g. AsO^2‐ to AsO₄ ^3‐) or reduction (e.g. Hg²⁺ to Hg⁰) can enzymatically and intracellularly convert a more toxic form of an element to a less toxic form.

3. The biosynthesis of intracellular polymers which serve as traps for the removal of metal ions from solution such as traps have been described for cadmium, calcium, nickel and copper.

4. The binding of metal ions to cell surfaces.

5. The precipitation of insoluble metal complexes (e.g. metal sulfides and metal oxides) at cell surfaces.

6. Biomethylation and transport through cell‐membranes by diffusion controlled processes.

In this short review I shall discuss the implications of biomethylation as a detoxification mechanism for microorganisms as well as for certain higher organisms.