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1.
A process was developed to separate fiber from distillers dried grains with solubles (DDGS) in a dry‐grind corn process. Separation of fiber from DDGS would provide two valuable coproducts: 1) DDGS with reduced fiber, increased fat, and increased protein contents; and 2) fiber. The process, called elusieve process, used two separation methods, sieving and elutriation, to separate the fiber. Material carried by air to the top of the elutriation column was called the lighter fraction and material that settled to the bottom of the column was called the heavier fraction. We evaluated the compositions of fractions produced from sieving and elutriation. Two commercial samples of DDGS were obtained from two dry‐grind corn plants. Sieving over four screens (869, 582, 447, and 234 μm openings) created five size categories. The two smallest size categories contained >40% (w/w) of the original DDGS and had reduced fiber and increased protein and fat contents relative to the original DDGS. Elutriation of the remaining three size categories increased protein and fat contents and reduced fiber contents in the heavier fractions. Elutriation at air velocities of 1.59–5.24 m/sec increased the protein content of the heavier fraction by 13–41% and increased the fat content of the heavier fraction by 4–127% compared with the bulk fractions of each size category. This process was effective in separating fiber from both DDGS samples evaluated. Elusieve process does not require changes in the existing dry‐grind process and can be implemented at the end of the dry‐grind process.  相似文献   

2.
Separation of fiber from distillers dried grains with solubles (DDGS) provides two valuable coproducts: 1) enhanced DDGS with reduced fiber, increased fat and increased protein contents and 2) fiber. Recently, the elusieve process, a combination of sieving and elutriation was found to be effective in separating fiber from two commercial samples of DDGS (DDGS‐1 and DDGS‐2). Separation of fiber decreased the quantity of DDGS, but increased the value of DDGS by increasing protein content and produced a new coproduct with higher fiber content. Economic analysis was conducted to determine the payback period, net present value (NPV), and internal rate of return (IRR) of the elusieve process. The dependence of animal foodstuff prices on their protein content was determined. Equipment prices were obtained from industrial manufacturers. Relative to crude protein content of original DDGS, crude protein content of enhanced DDGS was higher by 8.0% for DDGS‐1 and by 6.3% for DDGS‐2. For a dry‐grind plant processing corn at the rate of 2,030 metric tonnes/day (80,000 bushels/day), increase in revenue due to the elusieve process would be $0.4 to 0.7M/year. Total capital investment for the elusieve process would be $1.4M and operating cost would be $0.1M/year. Payback period was estimated to be 2.5–4.6 years, NPV was $1.2–3.4M, and IRR was 20.5–39.5%.  相似文献   

3.
Data are presented for 32 elements (Li, Be, B, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Ge, As, Rb, Sr, Y, Zr, Mo, Ag, Cd, Sb, Cs, Ba, La, Ce, Pr, Nd, Sm, Hf, Tl, Pb, Bi) in organic-rich surface soils in Norway, based on samples from 464 sites. By considering geographical distributions based on isopleths, results from factor analysis, and ANOVA of median values from 12 different geographical regions, the contributions from natural and anthropogenic sources are estimated for each element. Long-range atmospheric transport of pollutants from areas out of Norway is a dominant source for Cd, Sb, Pb, and Bi and also a strongly contributing factor for Zn, As, Mo, and Tl. Also V, Ni, Cu, and Ge are somewhat affected, but other factors dominate for these elements. Local point sources of pollution provide significant contributions to soil concentrations of Ni, Cu, Zn, As, Mo, and Cd. The local bedrock is the overriding source of Li, Be, Ti, V, Cr, Mn, Rb, Zr, Cs, Ba, REE, Hf, and probably of Ge and Ag. Surface enrichment by root uptake in plants and return to the soil surface by decaying plant material is particularly evident for Mn, Zn, Rb, Cs, and Ba. These elements show no clear difference between south and north in the country, indicating that their plant uptake does not depend on latitude. In the case of B and Sr, atmospheric deposition of marine aerosols is an important source. Rb and Ag, and to a less extent Mn, Ga, and Ba, appear to be depleted in soils near the coast presumably due to cation exchange with airborne marine cations.  相似文献   

4.
The multi-element (Ag, Al, Au, Ba, Bi, Ca, Cd, Co, Cr, Cs, Cu, Dy, Er, Fe, Ga, Gd, Ho, In, Ir, La, Lu, Mn, Mo, Nb, Nd, P, Pb, Pd, Pr, Pt, Rb, Re, Rh, Ru, Sb, Sc, Sm, Sn, Sr, Ta, Tb, Th, Ti, Tl, Tm, U, V, Y, Yb, and Zn) concentrations (microg/kg, fresh weight) in potatoes (Solanum tuberosum, Folva) were investigated in this study. The potatoes were grown in two fertilization practices; one with pig slurry and one with calcium ammonium nitrate at three levels of N fertilization (0, 60, and 120 kg of N/ha). The experiment field was located at the Riso National Laboratory Agronomy Farms in Roskilde, Denmark. High-resolution-inductively coupled plasma mass spectrometry (HR-ICPMS) was used for analyses of the samples. The effect of three levels of N fertilization on elemental concentrations of the crop are evaluated by use of discriminant partial least-squares regression (PLS). The results provide useful biological and nutritional information on potatoes.  相似文献   

5.
以北京市土壤重金属背景值为标准,对比分析了农业土壤中Cr、Ni、Cu、Zn、As、Cd、Ph、Hg 8种重金属的含量及累积情况,并采用单因子污染指数法和综合污染指数法进行了土壤重金属污染评价。结果表明,北京市农业土壤存在着一定的Cr、Cu、Zn、As、Cd累积趋势,其含量的平均值分别为53．61、21．95、65．42、9．14、0．125mg·kg^-1,比相应的背景值高79．9％、17．4％、13．8％、28．9％、5．0％;Ni和Pb的累积则不明显,平均值比相应的背景值低7．9％、29．2％,分别为24．84和19．04mg·kg^-1;而Hg含量的平均值与背景值一致,为0．08mg·kg^-1。从单因子评价结果来说,Cr污染指数在1．06-2．93之间,所有的样点都处于轻度或中度污染状态;As、Cu、Zn、Cd的污染指数相对较小,平均值分别为1．29、1．17、1．13、1．05,有50％以上的样点处于轻度污染状态;而Ni、Ph、Hg的污染指数均小于1,有60％以上的样点处于清洁或尚清洁状态,污染较轻。若从综合评价结果来说,综合污染指数处于0．96～2．16之间,平均值为1．45,几乎所有的土壤样点都属于轻度污染状态。  相似文献   

6.
Odor volatiles in three major lychee cultivars (Mauritius, Brewster, and Hak Ip) were examined using gas chromatography-olfactometry, gas chromatography-mass spectrometry, and gas chromatography-pulsed flame photometric detection. Fifty-nine odor-active compounds were observed including 11 peaks, which were associated with sulfur detector responses. Eight sulfur volatiles were identified as follows: hydrogen sulfide, dimethyl sulfide, diethyl disulfide, 2-acetyl-2-thiazoline, 2-methyl thiazole, 2,4-dithiopentane, dimethyl trisulfide, and methional. Mauritius contained 25% and Brewster contained 81% as much total sulfur volatiles as Hak Ip. Cultivars were evaluated using eight odor attributes: floral, honey, green/woody, tropical fruit, peach/apricot, citrus, cabbage, and garlic. Major odor differences in cabbage and garlic attributes correlated with cultivar sulfur volatile composition. The 24 odor volatiles common to all three cultivars were acetaldehyde, ethanol, ethyl-3-methylbutanoate, diethyl disulfide, 2-methyl thiazole, 1-octen-3-one, cis-rose oxide, hexanol, dimethyl trisulfide, alpha-thujone, methional, 2-ethyl hexanol, citronellal, (E)-2-nonenal, linalool, octanol, (E,Z)-2,6-nonadienal, menthol, 2-acetyl-2-thiazoline, (E,E)-2,4-nonadienal, beta-damascenone, 2-phenylethanol, beta-ionone, and 4-vinyl-guaiacol.  相似文献   

7.
Twenty-four Spanish thyme honey samples were analyzed using inductively coupled plasma optical emission spectrometry (ICP-OES). Twenty-four minerals were quantified for each honey. The elements Al, As, Ba, Ca, Cr, Cu, Fe, K, Li, Mg, Mn, Na, P, Pb, S, Se, Si, Sr, and Zn were detected in all samples; seven elements are very abundant (Ca, K, Mg, Na, P, S, and Si), and six are not abundant (Al, Cu, Fe, Li, Mn, and Zn). Eleven of them are trace elements (As, Ba, Cd, Co, Cr, Ni, Mo, Pb, Se, Sr, and V) at <1 mg kg(-)(1). Classification of thyme honeys according to their origin (coast, mountains) was achieved by pattern recognition techniques on the mineral data. By means of principal component analysis, a good separation by geographical origin is obtained when scores for the two first principal components are plotted. Classification functions of 11 metals (Al, As, Cr, Cu, K, Li, Mg, Na, P, S, and V) were obtained using stepwise discriminant analysis and applied to classify correctly approximately 100% of the honey samples.  相似文献   

8.
Bioactivity-guided fractionation of black bean (Phaseolus vulgaris) seed coats was used to determine the chemical identity of bioactive constituents, which showed potent antiproliferative and antioxidative activities. Twenty-four compounds including 12 triterpenoids, 7 flavonoids, and 5 other phytochemicals were isolated using gradient solvent fractionation, silica gel and ODS columns, and semipreparative and preparative HPLC. Their chemical structures were identified using MS, NMR, and X-ray diffraction analysis. Antiproliferative activities of isolated compounds against Caco-2 human colon cancer cells, HepG2 human liver cancer cells, and MCF-7 human breast cancer cells were evaluated. Among the compounds isolated, compounds 1, 2, 6, 7, 8, 13, 14, 15, 16, 19, and 20 showed potent inhibitory activities against the proliferation of HepG2 cells, with EC50 values of 238.8 +/- 19.2, 120.6 +/- 7.3, 94.4 +/- 3.4, 98.9 +/- 3.3, 32.1 +/- 6.3, 306.4 +/- 131.3, 156.9 +/- 11.8, 410.3 +/- 17.4, 435.9 +/- 47.7, 202.3 +/- 42.9, and 779.3 +/- 37.4 microM, respectively. Compounds 1, 2, 3, 5, 6, 7, 8, 9, 10, 11, 14, 15, 19, and 20 showed potent antiproliferative activities against Caco-2 cell growth, with EC50 values of 179.9 +/- 16.9, 128.8 +/- 11.6, 197.8 +/- 4.2, 105.9 +/- 4.7, 13.9 +/- 2.8, 35.1 +/- 2.9, 31.2 +/- 0.5, 71.1 +/- 11.9, 40.8 +/- 4.1, 55.7 +/- 8.1, 299.8 +/- 17.3, 533.3 +/- 126.0, 291.2 +/- 1.0, and 717.2 +/- 104.8 microM, respectively. Compounds 5, 7, 8, 9, 11, 19, 20 showed potent antiproliferative activities against MCF-7 cell growth in a dose-dependent manner, with EC50 values of 129.4 +/- 9.0, 79.5 +/- 1.0, 140.1 +/- 31.8, 119.0 +/- 7.2, 84.6 +/- 1.7, 186.6 +/- 21.1, and 1308 +/- 69.9 microM, respectively. Six flavonoids (compounds 14-19) showed potent antioxidant activity. These results showed the phytochemical extracts of black bean seed coats have potent antioxidant and antiproliferative activities.  相似文献   

9.
The aim of the present study was to estimate the geochemical background and anomaly threshold values of the surface soils in Kavala, northern Greece. In order to reach this goal, a simple and practical procedure was applied. This procedure included the extraction of 42 major and trace elements by analytical grade HNO3 from 65 surface soil samples, analysis by inductively coupled plasma?Coptical emission spectrometry and inductively coupled plasma?Cmass spectrometry, the distribution of the elemental data displayed on probability graphs (Q-Q plots), and the visualization of the results spatially by GIS software. The results indicated that natural factors mostly influence the elevated concentrations of Al, Ca, Fe, K, Mg, Si, B, Ba, Ce, Ga, Ge, La, Li, Mn Rb, Sb, Se, Sn, Sr, Y, and Zr, while anthropogenic activities mostly influence the elevated concentrations of Ag, As, Cd, Co, Cr, Cs, Cu, Hg, Mo, Ni, Pb, Th, Ti, U, V, W, and Zn. Nevertheless, almost all the elements determined showed their elevated concentrations inside the industrial part of Kavala area, which implies that the anthropogenic activities taking place in the study area, influence importantly the spatial distribution of the elements. The methodology followed in this research seems to be an adequate alternative for soil environmental studies.  相似文献   

10.
不同原料好氧发酵产生的臭气物质组分和浓度存在差异。以牛粪和玉米秸秆为原料研究好氧发酵过程挥发性有机物（Volatile Organic Compound，VOCs）的产排特征及主要致臭物质，开展牛粪好氧发酵试验，采用气相色谱-质谱法分析测定发酵升温期、高温期、降温期及腐熟期等不同发酵阶段的VOCs组分和浓度，硼酸溶液吸收，盐酸滴定法测定NH3，便携式检测器（Tion NH3-H2S 300 G）测定H2S，3点比较式臭袋法测定不同发酵阶段臭气浓度。结果表明，牛粪好氧发酵过程中共检出31种VOCs，其中含硫化合物42种，醇类1种，酯类1种，酮类1种，卤代烃4种，苯系物9种，烷烃类8种，烯烃3种；在好氧发酵高温期臭气浓度最高为724（无量纲），VOCs产生与排放主要在高温期。基于恶臭污染排放标准和恶臭物质气味活度值，并结合各物质检出率、GS-MS图谱及相关性分析，发现NH3、H2S、甲硫醚是牛粪好氧发酵过程的主要致臭物质；其次芳香族化合物对臭气浓度贡献也相对较大，应进行重点监测与控制。该研究可为牛粪好氧发酵过程臭气物质减控提供理论支撑。  相似文献   

11.
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12.
Abstract

Periods of maximum hard red spring (HRS) wheat (Triticum aestivum L.) nutrient demand need to be determined in order to develop best nutrient management practices, and to provide data for nutrient uptake modeling. Aerial (aboveground biomass) whole plant samples of irrigated HRS wheat were collected from the field at 16 growth stages and separated into leaves, stems, heads, and grain for dry matter determinations and analyzed for nitrogen (N), phosphorus (P), potassium (K), calcium (Ca), magnesium (Mg), sulfur (S), chloride (Cl), zinc (Zn), manganese (Mn), iron (Fe), and copper (Cu) concentrations. Accumulation curves were computed for each plant part for the growing season from compound cubic polynomial models based on accumulated growing degree units (GDUs). Total aerial accumulations of dry matter, N, P, K, Ca, Mg, S, Cl, Zn, Mn, Fe, and Cu were 14400, 116, 30.8, 103, 9.2, 9.3, 15.2, 32.3, 0.18, 0.58, 2.05, and 0.045 kg/ha, respectively. Grain at maturity accumulated greater than 78% of the total aerial N, P, and Zn, while it contained less than 20% of the aerial accumulated K, Ca, Cl, and Fe. Nitrogen and Fe were rapidly accumulated near 200 GDU, while P, K, Ca, Mg, S, Cl, Zn, Mn, and Cu were most rapidly accumulated near 600 GDU. Accumulation rates were 183, 2.9, 0.90, 0.72, 0.008, 1.41, 0.29, and 0.12 kg/ha/d for dry matter, N, P, K, Ca, Mg, S, and Cl, respectively, and 136, 1.7, 0.48, 0.13, 0.004, 0.78, 0.20, and 0.02 g/ha/d, respectively, during grainfill. This plant information suggests the timing of in‐season nutrient applications and, when integrated with other agronomic practices, could improve overall nutrient management for HRS wheat in the northern Great Plains.  相似文献   

13.
华北某些旱地硫库的组成   总被引：1，自引：0，他引：1  
Soil sulfur fractions,including monocalcium phosphate-extractable S,slowly soluble inorganic S,C-O-S,C-bonded S and unidentified organic S,were analyzed for 48 soils,as representatives of 6 major groups of upland soils,fluvisol,cinnamon soil,loessial soil,chestnut soil,black soil and brown soil,in North china,The contents of total S and monocalcium phosphate-extractalble S in the above 48 soils ranged from 234 to 860 and 5.1to 220.3mg kg^-1,respectively and each of 6 soil groups contained the samples with a low level of phosphate-extractable S.Great differences in the average contents of each fraction of S were observed among the above 6 soil groups.Expressed as average percentage of the total S in soils,fluvisols,cinnamon soils,loessial soils,chestnut soils,black soils and brown soils contained 6.1%,9.5%,5.7%,13.2%,3.5%and 6.8% monocalcium phosphate-extractable S,5.7%,3.0%,9.3%,10.4%,3.2%and 3.1% slowly soluble inorganic S,51.6%,26.7%,17.4%,31.2%,28.9%and 22.7% C-O-S,11.0%,9.1%,6.6%,6.8%,9.7%and 9.4% in C-bonded S,and 25.6%,51.7%,60.8%,38.4%,54.7%and 53.0% unidentifed organic S,respectively,FOr the above 6 groups of soils,the mean C/N ratios were remarkably similar,ranging from 9.7 to 10.7,while the mean N/S ratios ranged from 1.16 to 3.12,The highest ratios of C/N,C/C-O-S and C/C-bonded S were found in black soils.averaging 30.4,104.9and 314.7,respectively,while the lowest ratios arose in chestnut soil,averaging 12.4,39.7 and 183.3,respectively.  相似文献   

14.
Different sample preparation methods were evaluated for the simultaneous multielement analysis of wine samples by inductively coupled plasma optical emission spectrometry (ICP-OES) and inductively coupled plasma mass spectrometry (ICP-MS). Microwave-assisted digestion in closed vessel, thermal digestion in open reactor, and direct sample dilution were considered for the determination of Li, Be, Na, Mg, Al, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Sr, Y, Mo, Cd, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Tl, Pb, and Bi in 12 samples of red wine from Valencia and Utiel-Requena protected designation of origin. ICP-MS allows the determination of 17 elements in most of the samples, and using ICP-OES, a maximum of 15 elements were determined. On comparing the sample pretreatment methodology, it can be concluded that the three assayed procedures provide comparable results for the concentration of Li, Na, Mg, Al, K, Ca, Mn, Fe, Zn, and Sr by ICP-OES. Furthermore, ICP-MS data found for Cu, Pb, and Ba were comparable. Digestion treatment provides comparable values using both total decomposition in open system and microwave-assisted treatment for Cu by ICP-OES and for Cr, Ni, and Zn by ICP-MS. Open vessel total digestion provides excess values for Cr, Mn, Fe, and Zn by ICP-OES and defect values for Se. However, direct measurement of diluted wine samples provided uncomparable results with the digestion treatment for Mn, Cu, Pb, Zn, Ba, and Bi by ICP-OES and for Mg, Cr, Fe, Ni, and Zn by ICP-MS. Therefore, it can be concluded that microwave-assisted digestion is the pretreatment procedure of choice for elemental analysis of wine by ICP-based techniques.  相似文献   

15.
石灰和绿肥对不同种植制度植烟酸性土壤改良效果   总被引：3，自引：1，他引：2  
为寻求酸性植烟土壤可持续改良方法,采用大田试验研究了石灰、石灰+绿肥在烤烟连作、烤烟与玉米轮作方式上对酸性植烟土壤物理特性、主要养分和酸度特征指标的影响,并分析了土壤pH与土壤理化指标的相关性。结果表明:在烤烟连作方式下,施用石灰并结合种植绿肥还田改良酸性土壤比单施石灰效果好,能使土壤容重、水解性酸、交换性酸、交换性氢和交换性铝分别降低11.97%,25.00%,18.46%,21.74%和16.67%,土壤孔隙度、有机质、碱解氮、有效磷、速效钾含量、pH、阳离子交换量、盐基饱和度和土壤缓冲容量分别提高42.26%,57.02%,11.86%,16.39%,50.65%,5.97%,8.05%,13.17%和81.90%。施用石灰并结合种植绿肥对烤烟与玉米轮作方式的酸性土壤修复效果较烤烟连作更好,土壤容重、水解性酸、交换性酸、交换性氢和交换性铝可分别降低4.00%,20.51%,27.92%,10.00%和37.14%,土壤孔隙度、有机质、碱解氮、有效磷、速效钾含量、pH、阳离子交换量、盐基饱和度和土壤缓冲容量可分别提高9.17%,13.97%,7.22%,12.06%,5.08%,5.15%,35.27%,15.44%和28.05%。石灰+绿肥协同改良酸性土壤的效果比单施石灰好,烤烟与玉米轮作较烤烟连作更有利于酸化土壤的修复。研究结果为采用石灰和种植绿肥还田改良酸性土壤提供了理论依据和实践指导。  相似文献   

16.
我国几种土壤中铁锰结核的元素组成和地球化学特点   总被引：7，自引：0，他引：7  
The objective of this research was to isolate a dichlorvos （2,2-dichlorovinyl dimethyl phosphate）-degrading strain of Ochrobactrum sp., and determine its effectiveness in remediation of a dichlorvos-contaminated soil. A dichlorvos-degrading bacterium （strain DDV-1） was successfully isolated and identified as an Ochrobactrum sp. based on its 16S rDNA sequence analysis. Strain DDV-1 was able to utilize dichlorvos as a sole carbon source, and the optimal pH and temperature for its cell growth and degradation were 7.0 and 30 ℃, respectively. Also, the growth and degradation of strain DDV-1 showed the same response to dissolved oxygen. In addition, the soil degradation test indicated that in soil spiked with 100 mg L^-1 or 500 mg L^-1 dichlorvos and inoculated with 0.5% or 1.0% （v/v） strain DDV-1, complete degradation of dichlorvos could be achieved in 24 h. The present study showed that strain DDV-1 was a fast dichlorvos-degrading bacterium in soil. However, further research will be needed to clarify the degradation pathway and the properties of the key enzymes involved in its biodegradation.  相似文献   

17.
Soil samples taken by soil auger to a depth of 150 mm from randomly selected agricultural fields throughout England and Wales were analysed for total As, B, Cd, Co, Cr, Cu, Hg, Ni, Pb, Se and Zn, acetic acid-extractable Cd, Co, Cu, Ni, Pb and Zn, EDTA-extractable Cd, Co, Cu, Ni, Pb, Se and Zn, ammonium oxalate extractable Ni and Mo and hot water-extractable B. Median, log-derived mean and range data are given for each element. Median values are given also by parent material and textural grouping.  相似文献   

18.
基于YOLOv5s的深度学习在自然场景苹果花朵检测中的应用   总被引：5，自引：5，他引：0  
疏花是苹果栽培的重要管理措施,机械疏花是目前最具有发展潜力的疏花方式,花朵的高效检测是疏花机器人高效作业的重要保障。该研究基于机器视觉与深度学习技术,提出了一种基于YOLOv5s深度学习的苹果花朵检测方法,在对田间拍摄得到的苹果花朵图像标注后,将其送入微调的YOLOv5s目标检测网络进行苹果花朵的检测。经测试,模型的精确率为87.70%,召回率为0.94,均值平均精度(mean Average Precision, mAP)为97.20%,模型大小为14.09 MB,检测速度为60.17 帧/s,与YOLOv4、SSD和Faster-RCNN模型相比,召回率分别提高了0.07、0.15、0.07,mAP分别提高了8.15、9.75和9.68个百分点,模型大小减小了94.23%、84.54%、86.97%,检测速度提升了126.71%、32.30%、311.28%。同时,该研究对不同天气、颜色和光照情况下的苹果花朵进行检测,结果表明,该模型对晴天、多云、阴天、小雨天气下苹果花朵的检测精确率分别为86.20%、87.00%、87.90%、86.80%,召回率分别为0.93、0.94、0.94、0.94,mAP分别为97.50%、97.30%、96.80%、97.60%。该模型检测白色、粉色、玫红色和红色花朵的精确率分别为84.70%、91.70%、89.40%、86.90%,召回率分别为0.93、0.94、0.93、0.93,mAP分别为96.40%、97.70%、96.50%、97.90%。该模型检测顺光和逆光条件下苹果花朵的精确率分别为88.20%、86.40%,召回率分别为0.94、0.93,mAP分别为97.40%、97.10%。结果表明YOLOv5s可以准确快速地实现苹果花朵的检测,模型具有较高的鲁棒性,且模型较小,更有利于模型的迁移应用,可为疏花器械的发展提供一定的技术支持。  相似文献   

19.

Purpose

Human exposure to particulate matter emitted from on-road motor vehicles includes complex mixtures of heavy metals from tyres, brakes, part wear, and resuspended road sediment. The purpose of this study was to determine the concentrations of 14 platinum-group and other traffic-related heavy metals in road sediment within the metropolitan area of Guangzhou, China, with a view to identifying their sources and assessing the extent of anthropogenic influence on heavy metal contamination of road sediment.

Materials and methods

Thirty-five samples of road sediment were collected. The concentrations of Cr, Mn, Ni, Cu, Zn, La, Ce, Mo, Cd, Pb, Ba, and Rh were measured by inductively coupled plasma?Cmass spectrometry. Pt and Pd were analyzed by isotopic dilution?Cinductively coupled plasma?Cmass spectrometry. Multivariate statistical analysis and enrichment factor methods were employed to identify the sources of these heavy metals and to assess anthropogenic influences on their occurrence.

Results and discussion

The mean concentrations of Pt, Pd, Rh, Cr, Mn, Ni, Cu, Zn, La, Ce, Mo, Cd, Pb, and Ba in the road sediment samples were 68.24, 93.15, 23.85, 147.5, 712.3, 47.24, 177.5, 1254, 47.50, 96.62, 4.91, 3.00, 198.1, and 641.3?ng?g?1, respectively. Very weak to significant linear positive correlations were found among the various heavy metals. The elemental composition of road sediment was dominated by five principal components. Three clusters were identified through cluster analysis, and enrichment factors were calculated relative to soils in China. The sources and degree of contamination of the heavy metals are discussed based on the results.

Conclusions

The mean concentrations of heavy metals are higher than background values, especially for Pt, Pd, Rh, Cd, and Zn. Four main sources are identified: (1) Pt, Pd, and Rh were derived from traffic sources; (2) La, Ce, Mn, and Ba were derived mainly from natural sources; (3) Cr, Ni, Cu, Mo, Cd, and Pb showed mixed traffic-industry sources; and (4) Zn originated mainly from industrial sources. Enrichment factor analysis supported this source identification and further indicated that contamination of road sediment in Guangzhou is extremely high for Pt, Pd, and Rh; moderate to very high for Cd, Zn, Pb, Cu, and Mo; and minimal for Cr, Ni, La, Ce, and Ba.  相似文献   

20.
The objective of this research was to identify chemical, physical, bacteriological, and viral contaminants, and their sources, which present the greatest health threat in public ground water supplies in the USA; and to classify (prioritize) such contaminants and relative to their health concerns. The developed contaminant prioritization methodology was based on frequency of occurrence and adverse health effects. Adverse health effects were based on carcinogenic potency, toxicity, hazardous chemical priorities and drinking water standards. Application of the methodology for wellhead protection areas, (WHPAs) revealed that approximately 200 different contaminants have been detected in the nation's public ground water supplies. The seven chemical constituents with the highest priority were arsenic, chromium, cadmium, carbon tetrachloride, chloroform, 1, 1-dichloroethylene, and ethylene dibromide. Other contaminants of concern were trichloroethylene, nitrates, barium, 1,1,1-trichloroethane, benzene, tetrachloroethylene, selenium, lead, toluene, mercury, gross alpha radiation, methylene chloride, coliform bacteria, metolachlor, metribuzin, 1, 1, 2, 2-tetrachloroethane, dibromochloroethane, simazine, radium-266, and toxaphene. The contaminant source prioritization methodology was also based on frequency of occurrence. Over 30 categories of sources were evaluated, with the eight with highest priority including agricultural activities, hazardous waste sites, landfills, industrial operations, septic tank systems, oil and gas field activities, urban land use, and underground storage tanks.  相似文献   

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