Decomposition of 2,2',4,4',5,5'-hexachlorobiphenyl with iron supported on an activated carbon from an ion-exchange resin

An activated carbon (AC) containing a high concentration (374 mg g⁻¹) of Fe was prepared by carbonization of an ion-exchange resin. To examine its chemical reactivity as a catalyst to decompose 2,2′,4,4′,5,5′-hexachlorobiphenyl (PCB-153), the decomposition parameters of temperature and time were varied under air or N₂. Decomposition at 350 °C was achieved within 15 min under air and 30 min under N₂, and the efficiency of PCB-153 decomposition was 99.7% and 98.0%, respectively. An analysis of inorganic chloride ions revealed that PCB-153 was mineralized effectively during the decomposition. The Brunauer-Emmett-Teller (BET) surface area and pore volume of the AC were measured to assess the adsorption capacity before and after the decomposition. The differences between decomposition under air and N₂ reflected the differences in the BET surface and pore volume measurements. A decomposition pathway was postulated, and the reactive characteristics of chlorine atoms loaded on the benzene rings followed the order of para > meta > ortho, which agrees with the calculated results from a density functional theory study.     

Sorption of PAHs and PCBs to activated carbon: coal versus biomass-based quality

The addition of activated carbon (AC) is an increasingly popular method for pollutant immobilization, and the AC material can be made of biomass or coal/fossil feedstock. The aim of the present study was to investigate whether there are differences between pollutant sorption to biomass and coal-based AC in the presence and absence of sediment. Through N₂ and CO₂ adsorption to probe surface area and pore size it was shown that the biomass-based AC had a stronger dominance of narrow pores in the size range 3.5-15 Å than the anthracite-based material. In the absence of sediment, sorption isotherms for the probe compounds pyrene and PCB-101 showed stronger sorption for the biomass-based AC (logarithmic Freundlich coefficients 8.15 for pyrene; 9.91 for PCB-101) than for the anthracite-based one (logarithmic Freundlich coefficients 7.20 and 9.70, respectively). In the presence of sediment, the opposite trend was observed, with the stronger sorption for anthracite-based AC. Thus, the presence of competing and/or pore-blocking sediment constituents reduces sorption to a larger extent for biomass-derived AC (factor of 5 for pyrene to almost 100 for PCB-101) than for anthracite-based AC (no reduction for pyrene to factor of 5 for PCB-101). This difference is tentatively attributed to the difference in pore size distribution, narrow pores being more prone to clogging, and could have implications for remediation feasibility with AC from different sources.     

Long-term trends of continental-scale PCB patterns studied using a global atmosphere–ocean general circulation model

Continental-scale distribution and inter-continental transport of four polychlorinated biphenyl (PCB) congeners (28, 101, 153, 180) from 1950 to 2010 were studied using the global multicompartment chemistry transport model MPI-MCTM. Following identical primary emissions for all PCB congeners into air, most of the burden is stored in terrestrial (soil and vegetation) compartments. Thereby, PCB-28, PCB-101 and PCB-153 show a shift of the soil burden maxima from source to remote regions. This shift is downwind with regard to the westerlies for Eurasia and upwind for North America and more prominent for the lighter PCBs than for PCB-153 or PCB-180. In meridional direction, all congeners' distributions underwent a northward migration in Eurasia and North America since the 1950s. Inter-continental transport from Eurasian sources accounts largely for contamination of Alaska and British Columbia and determines the migration of the PCB distribution in soil in North America. Trans-Pacific transport occurs mainly in the gas phase in boreal winter (December-January-February) at 3-4 km altitude and is on a multi-year time scale strongly linked to the atmospheric pressure systems over the Pacific. Inter-continental transport of the lighter, more volatile PCBs is more efficient than for the heavier PCBs.     

Comparison of two reference black carbons using a planar PCB as a model sorbate

In studies assessing sorption of hydrophobic organic compounds (HOCs) in natural systems, the choice of an appropriate reference black carbon, which can represent environmental black carbon (BC), is essential. This study compared isotherms of two commonly available and distinct reference BCs (n-hexane soot (BCRM) and diesel particulate matter (SRM 2975)) and a natural sediment from a source with little black carbon (Lake Hartwell, SC) using 3,3',4-trichlorobiphenyl (IUPAC #35) as a model sorbate. There was greater sorptivity for PCB-35 by BCRM than by SRM 2975. The observed differences in sorption between the two reference black carbons for PCB-35 may be ascribed to the different chemical characteristics of the black carbons. Differences in pore volume distribution at <16A pore width are less likely to be responsible for the observed differences in sorption. The elemental analysis confirmed that BCRM was a pure n-hexane soot because only C, H and O were measured. In contrast, SRM 2975 also contained N and S and a higher O% than BCRM. Compared to the low BC sediment, the two reference BCs had greater pore volume distributions, surface areas, total pore volumes and sorption. The observed nF (i.e., Freundlich exponent) values for PCB indicated greater linearity of the isotherms for the natural sediment than for the reference black carbons. For designing studies of sorption of HOCs in natural systems, in particular, when PCBs are contaminants of concern, results of this study can aid selection of the appropriate reference BCs.     

Spatial variance in multimedia mass balance models: comparison of LOTOS-EUROS and SimpleBox for PCB-153

The aim of this study was to determine whether nested generic box models can be used to predict spatial variance. An inter-comparison study was performed for the nested box model SimpleBox, and the spatially resolved model LOTOS-EUROS, using PCB-153 emissions in Europe as an example. We compared the two models concerning (1) average environmental concentrations, (2) spatial concentration variances, (3) spatial concentration patterns (maps), and (4) agreement with measured concentrations for the air and soil compartments. In SimpleBox, the spatial concentration variances and patterns were calculated subsequently for each separate grid cell surrounded by a regional and a continental shell with homogeneous, averaged circumstances. Average European PCB-153 concentrations calculated by LOTOS-EUROS and SimpleBox for the period 1981-2000 agree well for the air and soil compartments. Moreover, the predicted concentrations of both models are in line with the measured PCB-153 concentrations in Europe during that period. For PCB-153, the prediction of spatial concentration variances with the nested multimedia fate model SimpleBox performs adequately in most cases, except for the lower concentration boundary in the air compartment. It is concluded that SimpleBox can be used to predict the spatial maximum and average concentrations of PCB-153 in the air and soil compartments. The proposed method has to be tested systematically for different types of compounds, emission scenarios, environmental compartments and spatial scales in order to allow conclusions about the general applicability of the method.     

Concentrations of organochlorine pesticides and polychlorinated biphenyls in human serum and their relation with age,gender, and BMI for the general population of Bizerte,Tunisia

Human serum samples (n?=?113) from Bizerte, northern Tunisia, collected between 2011 and 2012 were analyzed for 8 organochlorine pesticides (OCPs) including p,p′-dichlorodiphenyltrichloroethane (DDT) and its metabolites, hexachlorobenzene (HCB), hexachlorocyclohexane isomers, dieldrin, and heptachlor and 12 polychlorinated biphenyls (PCBs) congeners. Concentrations of these residues in serum were determined by gas chromatography with electron capture detector and total cholesterol (CHOL) and triglycerides (TG) levels were evaluated by enzymatic colorimetric method. HCB, p,p′-DDE, PCB-138, PCB-153, and PCB-180, were the most abundant organochlorine compounds (OCs) detected in >95 % of the study subjects. The mean levels of p,p′-DDE and HCB in serum were 168.8 and 49.1 ng?g^?1 lipid, respectively. The sum PCBs concentrations ranged from 37.5 to 284.6 ng?g^?1 lipid in the samples, with mean and median value of 136.1 and 123.2 ng?g^?1 lipid, respectively. The PCB profile consisted of persistent congeners, such as PCB-138, PCB-153, and PCB-180 which contributed for approximately 82.7 % to the ∑PCBs. Statistical analysis showed that most OCs correlated significantly with age, considering all samples together or with gender differentiation. The present study shows that the levels of p,p′-DDE and ∑DDTs were significantly higher in females than in males (p?<?0.05), while PCBs levels were significantly higher in male (p?<?0.05) than in females. No statistically significant association was found between body mass index and concentration of any organochlorine pesticide or PCB congeners 153, 138, 180, or ∑PCBs.     

Iron-mediated reactions of polychlorinated biphenyls in electrochemical peroxidation process (ECP)

A study was conducted to explore some of the basic processes of polychlorinated biphenyl (PCB) destruction by a new technology termed electrochemical peroxidation process (ECP). ECP represents an enhancement of the classic Fenton reaction (H2O2 + Fe2+) in which iron is electrochemically generated by steel electrodes. Focus was on the extent of adsorption of a mixture of Aroclor 1248 on steel electrodes in comparison to iron filings. Commercially available zero-valent iron filings rapidly adsorbed PCBs from an aqueous solution of Aroclor 1248. Within 4 h, all the PCBs were adsorbed at 1%, 5%, and 10% Fe0 (w/v) concentrations. Little difference in adsorption was found between acidic (2.3) and unamended solutions (pH 5.5), even though significant differences in iron oxidation state and Fe2+ concentrations were measured in solution. PCB adsorption also occurs on steel electrodes regardless of the pH or electric current applied (AC or DC), suggesting the combination of oxidizing (free radical-mediated reactions) and reducing (dechlorination reactions) iron-mediated degradation pathways may be possible. Extraction of the iron powder after 48 h of contact time yielded the progressive recovery of biphenyl with increasing Fe mass(from 0.4% to 3.5%) and changes of the PCB congener-specific pattern as a consequence of dechlorination. A variety of daughter congeners similar to those accumulated during anaerobic microbial dechlorination of Aroclor 1248 in contaminated sediments indicate preferential removal of meta- and para-chlorines.     

Uptake, translocation and metabolism of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) in maize (Zea mays L.)

A hydroponic experiment was conducted in the present study to investigate and compare plant uptake, translocation and metabolism of polybrominated diphenyl ethers (PBDEs) of BDE-15, BDE-28 and BDE-47 and polychlorinated biphenyls (PCBs) of PCB-15, PCB-28 and PCB-47 in maize. Root concentrations of BDE-15, BDE-28 and BDE-47 were consistently higher than PCB-15, PCB-28 and PCB-47, respectively. A significantly positive correlation was found between logRCF (root concentration factor) and logKow of these PBDEs and PCBs, suggesting a control role of their partitioning in plant uptake. The translocation factors (TFs, Cstem/Croot) of PBDEs were generally lower than those of PCBs of the same halogen-substitutions, demonstrating easier transport of PCBs than PBDEs. Metabolites mono-, di- and tri-BDEs and PCBs were detected, suggesting the existence of in vivo metabolism of PBDEs and PCBs in maize. Dehalogenation and rearrangement of halogen atoms were identified, and some similarities but also significant differences existed between the PBDEs and PCBs. PBDEs in maize were, in general, more susceptible to metabolism compared with PCBs of the same halogen-substitutions. This is the first comparative report on the uptake, translocation and metabolism of PBDEs and PCBs in plants.     

浸渍-碱性微波法载磁活性炭粉对壬基酚的吸附

利用浸渍-碱性微波法制备载磁粉末活性炭,通过等温吸附实验和动力学吸附实验,研究对比了其与原料活性炭、浸渍载铁活性炭对壬基酚的吸附性能。采用氮气吸附仪、FTIR、XRD、国标(GB/T12496.19-1999)邻菲啰啉分光度法及VSM,分别对3种样品进行了物相结构、表面官能团、铁含量及磁性能的分析,并探讨了吸附机理。结果表明,浸渍-碱性微波法载磁活性炭的总孔容及孔隙率均有较大提高;其吸附等温线符合Freundich方程,吸附动力学过程符合准二级动力学方程与孔道内扩散模型,相关系数R2均大于0.900。原活性炭经一定浓度的铁盐溶液浸渍后,铁含量由2%提高到8%。在碱性、N2气氛条件下微波后,铁系物主要存在形式为零价铁和Fe3O4,制得的载磁活性炭饱和磁化强度为1.12 emu/g。     

Organochlorine pesticides and polychlorinated biphenyl congeners in wild terrestrial mammals and birds from Chubu region, Japan: Interspecies comparison of the residue levels and compositions

In order to understand the residue levels of organochlorine compounds (OCs) and their accumulation patterns in wildlife inhabiting Chubu region, Japan, the concentrations of polychlorinated biphenyls (PCBs), hexachlorocyclohexane isomers (HCHs), DDT compounds (DDTs) and hexachlorobenzene (HCB) were measured in 8 species of terrestrial mammals and 10 species of birds. In view of feeding habits, the contamination levels of OCs were found to be higher in omnivorous mammals than in herbivorous ones, and in fish-eating ones and raptores than in omnivorous birds. In fox and dog, PCB-180 (2, 2′, 3, 4, 4′, 5, 5′-heptachlorobiphenyl) was the most dominant PCB congener, while in the other species PCB-153 (2, 2′, 4, 4′, 5, 5′-hexachlorobiphenyl) was the most persistent. The ratios of lower chlorinated PCB congeners (tri- to tetra-) to total PCBs were larger in fish-eating birds than in the other birds. The results indicate that the compositions of PCB congeners would reflect the differences of feeding habits and xenobiotic metabolizing systems among each species.     

孔结构和表面化学性质对活性炭吸附性能的影响

测定了室温下3种活性炭(GAC-C、GAC-P和GAC-T)对CO2、CH4和N2的吸附性能,并对颗粒活性炭孔结构和表面化学性质进行了表征,探讨了孔结构和表面化学性质对活性炭吸附性能的影响。结果表明:由于吸附机理、孔结构、表面含氧官能团和分子极性的差异,CO2、CH4和N2在活性炭上的饱和吸附量和吸附常数的关系为CO2>CH4>N2;CH4和N2的饱和吸附量主要受活性炭微孔孔容的影响,N2和CO2饱和吸附量的差异分别是由0.572～2.0 nm的微孔和0.4～6 nm的孔引起的;CH4吸附常数主要受较大中孔和大孔影响,N2吸附常数与微孔密切相关,大孔对CO2的吸附常数影响最大。     

Olive tree, Olea europaea L., leaves as a bioindicator of atmospheric PCB contamination

Olive tree leaf samples were collected to investigate their possible use for biomonitoring of lipophilic toxic substances. The samples were analyzed for 28 polychlorinated biphenyls (PCB) congeners. Twelve congeners were detected in the samples. PCB-60, 77, 81, 89, 105, 114, and 153 were the most frequently detected congeners ranging from 32 % for PCB-52 to 97 % for PCB-81. Σ₁₂PCBs concentration varied from below detection limit to 248 ng/g wet weight in the sampling area, while the mean congener concentrations ranged from 0.06 ng/g (PCB-128?+?167) to 64.2 ng/g wet weight (PCB-60). Constructed concentration maps showed that olive tree leaves can be employed for the estimation of spatial distrubution of these congeners.     

Adsorption of phenolics on activated carbon--impact of pore size and molecular oxygen

The impact of pore size of activated carbon fibers (ACFs) on adsorption capacity and on the potential for oligomerization of phenolic compounds on the surface of ACFs in the presence of molecular oxygen has been investigated in this study. Compared with granular activated carbon (GAC), ACFs have unique pore size distributions, suitable to be used to elucidate the effect of pore structure on adsorption. Adsorption isotherm data were collected for o-cresol and 2-ethylphenol on four ACFs (ACC-10, ACC-15, ACC-20, and ACC-25) with different micropore volumes and BET surface area and on one type of GAC bituminous base. These isotherms were collected under anoxic (absence of molecular oxygen) and oxic (presence of molecular oxygen) conditions. No significant impact of the presence of molecular oxygen on adsorption capacity was noted for ACC-10. ACC-10 has an average pore width of 19.2 A and total pore volume of 0.43 cm3g(-1). On the other hand, for the remaining ACFs, which have larger average pore width and larger pore volume, significant increase in the adsorptive capacity had been observed when molecular oxygen was present. The GAC gave the greatest difference between anoxic and oxic conditions when compared to all the ACFs studied. Binary adsorption of o-cresol and 2-ethylphenol on ACFs with the least pore size (ACC-10) also showed no significant differences between oxic and anoxic environment. The binary system under both anoxic and oxic conditions was well predicted by the ideal adsorbed solution theory (IAST).     

活性炭孔隙结构在其甲苯吸附中的作用

选用4种商用活性炭(AC),利用氮气绝热吸附、扫描电子显微镜(SEM)和傅立叶变换红外光谱(FTIR)测试了活性炭的物化性质。以甲苯为吸附质,在温度为298.15 K下进行了静态和动态吸附实验,研究了活性炭孔结构对其吸附性能、吸附行为、表面覆盖率和吸附能的影响。结果表明:活性炭的比表面积和孔容是其吸附性能主要影响因素,孔径在0.8～2.4 nm之间的孔容和甲苯吸附量之间存在较好的线性关系,且线性斜率随甲苯浓度增加而变大。甲苯吸附行为符合Langmuir吸附等温模型和准一阶动力学方程式。活性炭孔结构是甲苯吸附速率的主要制约因素。在甲苯快速吸附阶段,微孔为吸附速率主要制约因素,在甲苯颗粒内扩散阶段,微孔和表面孔为吸附速率的主要制约因素,在吸附末尾阶段,中孔和大孔为吸附速率的主要制约因素。4种活性积炭对甲苯的吸附能随其比表面变大而变大。     

Bioaccumulation of PCBs in Arctic seabirds: influence of dietary exposure and congener biotransformation

Four seabird species and their prey (zooplankton or fish) were collected in the Barents Sea to determine how dietary exposure, cytochrome P450 (CYP) enzyme activities and sex influenced their hepatic PCB concentrations and accumulation patterns. Five males and five females from each seabird species (little auk (Alle alle), Brunnich's guillemot (Uria lomvia), black guillemot (Cepphus grylle) and black-legged kittiwake (Rissa tridactyla)) were analysed. PCB concentrations could not be explained directly by carbon source (delta13C) or trophic position (delta15N), but by a combination of dietary parameters (delta13C, delta15N, migratory pattern, age) and contaminant metabolism. Contrary to previous studies, the PCB pattern differed among seabirds, with a higher proportion of persistent congeners (% of PCB-153, RPCB-153) in black-legged kittiwake than in auks. The PCB pattern also differed among auks, with little auk as the most efficient biotransformer (highest RPCB-153 values of persistent congeners). Based on high RPCB-153 values, Brunnich's guillemot poorly metabolised ortho-meta-unsubstituted congeners, whereas black guillemot poorly metabolised meta-para unsubstituted congeners. Species-specific differences in PCB biotransformation were confirmed by metabolic indices, where PCB patterns in seabirds were adjusted for PCB pattern in prey. The relative contribution of ortho-meta-unsubstituted congeners to SigmaPCBs decreased with increasing EROD activity. There were no differences in PCB concentrations, PCB patterns or cytochrome P450 enzyme activities between males and females. CYP P450 activities (CYP1A- and CYP2B/3A-like: EROD and testosterone 6beta-hydroxylation, respectively) were low and did not correlate with concentrations of non- or mono-ortho Cl-substituted PCBs (NO- and MO-PCBs), or with total toxic equivalent concentrations (TEQs) for dioxin-like effects of NO- and MO-PCBs.     

Concentration levels and congener profiles of polychlorinated biphenyls, pentachlorobenzene, and hexachlorobenzene in commercial pigments

The concentration levels and congener profiles of polychlorinated biphenyls (PCBs), pentachlorobenzene (PeCBz), and hexachlorobenzene (HxCBz) were assessed in commercially available organic pigments. Among the azo-type pigments tested, PCB-11, which is synthesized from 3,3′-dichlorobendizine, and PCB-52, which is synthesized from 2,2′,5,5′-tetrachlorobendizine, were the major congeners detected. It is speculated that these were byproducts of chlorobendizine, which has a very similar structure. The total PCB concentrations in this type of pigment ranged from 0.0070 to 740 mg/kg. Among the phthalocyanine-type pigments, highly chlorinated PCBs, mainly composed of PCB-209, PeCBz, and HxCBz were detected. Their concentration levels ranged from 0.011 to 2.5 mg/kg, 0.0035 to 8.4 mg/kg, and 0.027 to 75 mg/kg, respectively. It is suggested that PeCBz and HxCBz were formed as byproducts and converted into PCBs at the time of synthesizing the phthalocyanine green. For the polycyclic-type pigments that were assessed, a distinctive PCB congener profile was detected that suggested an impact of their raw materials and the organic solvent used in the pigment synthesis. PCB pollution from PCB-11, PCB-52, and PCB-209 pigments is of particular concern; therefore, the monthly variations in atmospheric concentrations of these pollutants were measured in an urban area (Sapporo city) and an industrial area (Muroran city). The study detected a certain level of PCB-11, which is not included in PCB technical mixtures, and revealed continuing PCB pollution originating from pigments in the ambient air.     

Ozonation of activated carbon and its effects on the adsorption of VOCs exemplified by methylethylketone and benzene

Ozonation can modify the surface property of an activated carbon such as specific surface area, pore volume, and functional group. Results indicate that ozonation can increase the specific surface area of an activated carbon from 783+/-51 to 851+/-25 m2/g due in part to increasing micropores (those below 15 A). However, there is no change in macropore and mesopore upon ozonation. The amount of oxygen functional group (OFG) increases from 197+/-4 to 240+/-4 microeq/g, mostly in hydroxyl and carboxyl groups upon ozone treatment. These oxygen-containing functional groups are stable in the temperature range 30-250 degrees C, but begin to decompose when temperature increases beyond 300 and 350 degrees C. When the temperature reaches 1200 degrees C, all OFGs virtually disappear. The effect of ozone treatment on the adsorption of volatile organic carbon (VOC) was exemplified by methylethylketone (MEK) and benzene. The adsorption density of MEK and benzene by ozone treated activated carbon (AC(O3)) are greater than that by the untreated (AC), with MEK being more adsorbable than benzene. Results of factorial analysis indicate that physical characteristics, namely, micropore, BET surface area, pore diameter (PD), micropore volume (MV) play an important role on benzene and MEK adsorption.     

Equilibrium and kinetics of adsorption of phosphate onto iron-doped activated carbon

Purpose

Two series of activated carbons modified by Fe (II) and Fe (III) (denoted as AC/N-Fe^II and AC/N-Fe^III), respectively, were used as adsorbents for the removal of phosphate in aqueous solutions.

Method

The synthesized adsorbent materials were investigated by different experimental analysis means. The adsorption of phosphate on activated carbons has been studied in kinetic and equilibrium conditions taking into account the adsorbate concentration, temperature, and solution pH as major influential factors.

Results

Maximum removals of phosphate are obtained in the pH range of 3.78?C6.84 for both adsorbents. Langmuir isotherm adsorption equation well describes the experimental adsorption isotherms. Kinetic studies revealed that the adsorption process followed a pseudo-second order kinetic model. Results suggest that the main phase formed in AC/N-Fe^II and AC/N-Fe^III is goethite and akaganeite, respectively; the presence of iron oxides significantly affected the surface area and the pore structure of the activated carbon.

Conclusions

Studies revealed that iron-doped activated carbons were effective in removing phosphate. AC/N-Fe^II has a higher phosphate removal capacity than AC/N-Fe^III, which could be attributed to its better intra-particle diffusion and higher binding energy. The activation energy for adsorption was calculated to be 22.23 and 10.89 kJ mol^?1 for AC/N-Fe^II and AC/N-Fe^III, respectively. The adsorption process was complex; both surface adsorption and intra-particle diffusion were simultaneously occurring during the process and contribute to the adsorption mechanism.     

Levels and temporal trends of chlorinated pesticides, polychlorinated biphenyls and brominated flame retardants in individual human breast milk samples from Northern and Southern Norway

Human breast milk samples from primipara women from Northern (Troms?) (N=10) and Southern Norway (Oslo) (N=19) collected in 2000-2001 were analysed with respect to hexachlorobenzene (HCB), hexachlorocyclohexane (HCHs), chlordanes (CHLs), DDTs, mirex, toxaphenes (CHBs), polychlorinated biphenyls (PCBs), polybrominated diphenylethers (PBDEs) and hexabromocyclododecane (HBCD). CHBs, PBDEs and HBCD were only analysed in the Troms? samples. Sum-PCBs and sum-DDTs were the major organochlorines (OCs) (170 and 110 ng g(-1) lipid weight (lw), respectively). Other OCs were found in levels of approximately 10- to 300-fold lower than sum-PCBs. Overall, the concentrations of OCs followed the decreasing order of PCBs>DDTs>HCB>HCHs approximately CHLs>CHBs>mirex. Concentrations of sum-HCHs were significantly higher in breast milk from Oslo compared to Troms? (p<0.05). The PCB profile was dominated by PCB-153, -138 and -180. The PBDE pattern was dominated by PBDE-47 and PBDE-153. The median level of sum-PBDEs was 4.1 ng g(-1) lw. PBDE-209 was detected in all analysed samples (median 0.13 ng g(-1) lw). The estimated daily intake (EDI) for the median (range) of sum mono-ortho (mo) PCBs(8) was 3.7 (1-9) pg TEQ kg(-1) body weight per day for breast fed infants in Norway. This exceeded the TDI by a factor of 1.8 (1-4) based only on intake of mono-ortho PCBs. The present study shows that concentrations of OCs in primipara breast milk have decreased 50-60% since 1991, and that this trend is continuing.     

废活性炭微波再生新工艺的研究

提出用微波加热-二氧化碳活化法再生乙酸乙烯合成用触媒载体废活性炭工艺.采用条件实验法研究了活化时间、二氧化碳流量和微波功率对活性炭碘吸附值,亚甲基蓝吸附值和再生得率的影响,得到微波辐射加热二氧化碳活化再生乙酸乙烯用触媒载体废活性炭的最佳工艺条件为活化时间25 min,二氧化碳流量0.2 L/min,微波功率700 W.在此条件下制得的活性炭碘吸附值为1158.02 mg/g、亚甲基蓝吸附值为240 mg/g、得率为74.19%.并对活性炭进行了比表面积的测定和孔结构的分析,活性炭的比表面积为1308.13 m2/g,总孔容为0.76 mL/g.