Circular economy practices among Chinese manufacturers varying in environmental-oriented supply chain cooperation and the performance implications

The rapidly growing industrial activities in emerging economies such as China have been causing resource depletion and pollution problems. This reality requires China to adopt an integrated management approach to resolve the conflict between industrial development and environmental protection, and the concept of circular economy (CE) serves this purpose. In this paper, we examine if different types of manufacturing enterprises on environmental-oriented supply chain cooperation (ESCC) exist. We also determine if the Chinese manufacturer types varying in ESCC differ in their implementation of the CE practices towards achieving the CE-targeted goals on improving both environmental and economic performance. Our cluster analytic results with multivariate analysis of variance (MANOVA) among the four identified types of Chinese manufacturers varying in environmental-oriented supply chain cooperation highlight the importance to intensify the cooperation with upstream and downstream supply chain partners for a CE initiative to succeed.     

生物法降解养殖场臭气中H_2S的反应器启动

畜禽养殖场臭气成分复杂,完全去除较为困难。生物法是目前应用较广泛的脱臭方法,其中能否将生物膜附着在填料上是影响生物法去除恶臭气体效率的重要因素。本实验采用定时定量投加Na2S的方式驯化活性污泥,并选用MLSS浓度和SO42-浓度增量变化2个指标作为污泥驯化成熟的指标,比传统的以MLSS作为污泥驯化成熟的指标更准确。采用循环污泥的挂膜方式,运行2 d后,通入新鲜的空气和H2S气体,2周后反应器启动成功。     

Suppression of Soot by Metal Additives During the Combustion of Polystyrene

This paper describes an experimental study on the suppression of soot by metal additives during the combustion of polystyrene (PS). A two-dimensional flame generated by using a Wolfhard-Parker type diffusion flame burner was used to simulate practical combustion situations. The PS was continuously fed to the burner and, by controlling the feed rate, the combustion was maintained at a steady state. The additives tested were the salts of Li, Na, K, Mg, Ca, Sr, and Ba, and the combinations of the salts of K and Ca, Sr, or Ba. These additives were added to the flame in the form of small drops of their aqueous solutions generated by an ultrasonic atomizer. Since the flow rate of the carrier gas (air) is very small, this addition causes no noticeable disturbance to the flame. The effectiveness of the alkali metals follows the order of their ease of ionization, i.e., K > Na > Li, and that of the alkaline-earth metals: Ba > Sr > Ca > Mg. At low addition rates, the effectiveness increases with increasing addition rate but becomes unaffected at high addition rates and the maximum percentage of soot suppressed is approximately 50 percent. The combinations of the two metals (i.e., K and Ca, Sr, or Ba) are much more effective than each single metal at the same addition rates and the maximum percentage of soot suppressed reaches approximately 90 percent. It is proposed that the alkaline-earth metals catalyze the ionization of the alkali metals, thus significantly enhancing the effect on soot suppression.     

Duo-molecularly imprinted polymer-coated magnetic particles for class-selective removal of endocrine-disrupting compounds from aqueous environment

The removal of steroid and phenolic endocrine-disrupting compounds (EDCs) from an aqueous environment was investigated using magnetic particles encapsulated by a duo-molecularly imprinted polymer (duo-MIP). The effect of environmental variables on the binding efficiency was studied. Experimental results showed that the amount of EDCs adsorbed was neither affected by up to 10.0 mM NaCl nor significantly interfered by up to 10.0 mg/L humic acid. Negligible influence was observed from pH 3.3 to pH 6.8, but a decrease started at pH 9. Freundlich isotherm parameters indicated binding capacities in the order of DES?>?E2?～?E1?>?BPA. The applicability of class-selective removal was verified using river water samples spiked with these EDCs at 10 μg/L; the binding efficiencies were 90, 90, 88, and 98 % for estrone (E1), 17β-estradiol (E2), bisphenol A (BPA), and diethylstilbestrol (DES), respectively. A reuse investigation verified constant binding capacities exhibiting <2 % reduction after seven cycles of regeneration.     

Mycelial growth and solid-state fermentation of lignocellulosic waste by white-rot fungus Phanerochaete chrysosporium under lead stress

Lignocellulosic biomass is an abundant renewable resource difficult to degrade. Its bioconversion plays important roles in carbon cycles in nature, which may be influenced by heavy metals in environment. Mycelial growth and the degradation of lignocellulosic waste by lignin-degrading fungus Phanerochaete chrysosporium under lead stress were studied. It was shown that P. chrysosporium could grow in liquid media with 400 mg L?1 Pb(II), and mycelial dry weight was reduced by 54% compared to the control. Yellow mycelia in irregular short-strip shape formed in Pb-containing media, whereas the control showed ivory-white regular mycelial pellets. Two possible responses to Pb stress were: dense hyphae, and secretion from mycelia to resist Pb. During solid-state fermentation of straw, fungal colonization capability under Pb stress was positively correlated with the removal efficiency of soluble-exchangeable Pb when its content was higher than 8.2 mg kg?1 dry mass. Carboxymethyl cellulase activity and cellulose degradation were inhibited at different Pb concentrations, whereas low Pb concentrations increased xylanase and ligninolytic enzyme activities and the hemicellulose and lignin degradation. Cluster analyses indicated that Pb had similar effects on the different microbial indexes related to lignin and hemicellulose degradation. The present findings will advance the understandings of lignocellulose degradation by fungi under Pb pollution, which could provide useful references for developing metal-polluted waste biotreatment technology.     

In vitro metabolism of hydroxylated polybrominated diphenyl ethers and their inhibitory effects on 17β-estradiol metabolism in rat liver microsomes

Purpose

Hydroxylated polybrominated diphenyl ethers (OH-PBDEs) have emerged as contaminants of environmental concerns because they pose potential risks to human and animal health. The purpose of this study was to investigate the in vitro metabolism of OH-PBDEs and their potential inhibition against 17??-estradiol (E2) metabolism.

Methods

Rat liver microsomes were used as a source of P450 enzymes in an in vitro metabolism study of OH-PBDEs. Inhibition of E2 metabolism and kinetic study were performed by incubating with rat liver microsomes in the presence of OH-PBDEs.

Results

The obtained data clearly demonstrated that OH-PBDEs, especially those congeners with lower bromination, could be metabolized to bromophenol and diOH-PBDEs. The less metabolic rate of OH-PBDEs was observed with the increasing number of bromine substituents. OH-PBDEs with hydroxyl group and bromine adjacent to the ether bridge showed faster metabolic rates. In addition, the results showed non-competitive inhibition of E2 metabolism by OH-PBDEs with IC₅₀ values in the range from 13.7 to 55.2???M. The most potent OH-PBDE inhibitor was found to be 3??-OH-BDE-100. The inhibitory potencies for OH-PBDEs were significantly higher than those of parent PBDE and methoxylated metabolites, providing the evidence that PBDEs exerted estrogenic activity in part by their hydroxylated metabolites.

Conclusions

OH-PBDEs exhibited large differences in their capacity to be metabolized and to inhibit E2 metabolism in rat liver microsomes. The finding might increase our understanding of healthy risk associated with PBDEs in human and wildlife.     

化学氧化法脱除石油焦中的硫

分别采用硝酸、硝酸-冰醋酸混合液以及王水作氧化剂脱除石油焦中的硫。实验结果表明:石油焦粒径越小,脱硫率越高;随液固比(氧化剂体积与石油焦质量比,mL/g)增大、反应时间延长、反应温度升高,脱硫率先增大,达到极值后保持稳定。王水的脱硫率高于硝酸和硝酸-冰醋酸混合液。王水脱除石油焦中硫的最佳工艺条件为:石油焦粒径0.1mm,液固比20mL/g,反应时间20h,反应温度50℃。在此最佳条件下,脱硫率达42.3%。经王水在最佳脱硫工艺条件下处理后,可有效脱除石油焦中大部分的噻吩类和硫醇类有机硫以及全部的无机硫。     

Effects of sintering atmosphere on cement clinkers produced from chromium-bearing sludge

The purpose of this study was to investigate the effects of sintering atmosphere (oxidizing and reducing) on the polymorphs of dicalcium silicates (Ca2SiO4, C2S) and on the chromium leaching of the belite-rich clinkers made from a chromium-bearing sludge. This sludge was generated in an electroplating factory, and in addition to chromium, it contained nickel, copper and zinc. In the clinker production, air was used as the oxidizing atmosphere, and carbon monoxide, which was produced by burning graphite with an insufficient amount of oxygen, was employed as the reducing atmosphere. Dicalcium silicates were substantially formed under both kinds of sintering atmosphere, but there was some nonhydraulic gamma-C2S in the clinkers produced under the oxidizing atmosphere. In addition, the amount of gamma-C2S decreased with the chromium-bearing sludge addition, whereas that of beta-C2S increased. The clinkers produced under the reducing atmosphere had less residual chromium, a finding that shows that more chromium was evaporated. However, the reducing atmosphere can decrease the proportion of hexavalent chromium (Cr(VI)) in the resulting clinkers. For other heavy metals, the residual amounts of nickel and copper generally increased with the sludge addition, but zinc was absent in most of the clinkers produced under the reducing atmosphere. This implies that the evaporation of zinc is much more significant than that of the other heavy metals under a reducing atmosphere. In the leaching tests, the concentrations of nickel, copper, and zinc were below the detection limits in all the leachates. In terms of chromium, the total leaching concentration was highly related to Cr(VI). The clinkers produced under the oxidizing atmosphere had high leaching concentrations of chromium, and thus failed to meet the regulatory limit. In contrast, the reducing atmosphere was effective in decreasing the chromium leaching, and it therefore makes the resulting cement clinkers more environmentally sound.     

Degradation of 3,3′-iminobis-propanenitrile in aqueous solution by Fe0/GAC micro-electrolysis system

The degradation of 3,3′-iminobis-propanenitrile was investigated using the Fe⁰/GAC micro-electrolysis system. Effects of influent pH value, Fe⁰/GAC ratio and granular activated carbon (GAC) adsorption on the removal efficiency of the pollutant were studied in the Fe⁰/GAC micro-electrolysis system. The degradation of 3,3′-iminobis-propanenitrile was affected by influent pH, and a decrease of the influent pH values from 8.0 to 4.0 led to the increase of degradation efficiency. Granular activated carbon was added as cathode to form macroscopic galvanic cells between Fe⁰ and GAC and enhance the current efficiency of the Fe⁰/GAC micro-electrolysis system. The GAC could only adsorb the pollutant and provide buffer capacity for the Fe⁰/GAC micro-electrolysis system, and the macroscopic galvanic cells of the Fe⁰/GAC micro-electrolysis system played a leading role in degradation of 3,3′-iminobis-propanenitrile. With the analysis of the degradation products with GC–MS, possible reaction pathway for the degradation of 3,3′-iminobis-propanenitrile by the Fe⁰/GAC micro-electrolysis system was suggested.     

Inhalation Transfer Factors for Air Pollution Health Risk Assessment

ABSTRACT

To facilitate routine health risk assessments, we develop the concept of an inhalation transfer factor (ITF). The ITF is defined as the pollutant mass inhaled by an exposed individual per unit pollutant mass emitted from an air pollution source. A cumulative population inhalation transfer factor (PITF) is also defined to describe the total fraction of an emitted pollutant inhaled by all members of the exposed population. In this paper, ITFs and PITFs are calculated for outdoor releases from area, point, and line sources, indoor releases in single zone and multizone indoor environments, and releases within motor vehicles. Typical PITFs for an urban area from emissions outdoors are ~10^-6–10^-3. PITFs associated with emissions in buildings or in moving vehicles are typically much higher, ~10^-3–10^-1.