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1.
采用低温等离子体和絮凝剂协同处理印染废水.结果表明,染料废水脱色率和COD去除率随输入电压增大和放电时间延长而增加;电极间距、废水初始浓度、通入空气流量等因素对印染废水处理效果也有很大影响;气相中放电效果优于液相中放电,阳极电极在液面以上8mm左右时放电效果最好,在其他条件不变情况下随废水初始浓度和通入空气流量增大废水脱色和COD脱除率先增大再减小,有一最佳峰值.印染废水先经过等离子体处理后再加入絮凝剂处理效果优于先加絮凝剂后放电、仅有等离子体放电的过程.在本实验中初始浓度200mg/L(CODCr初始值572)印染废水在外加电压40kV、放电时间20min、电极间距8mm、通入空气流量16L/h条件下,与絮凝剂PAC相互协同作用可达到96%脱色率、63%COD去除率. 相似文献
2.
Birinchi Bora Arun Kumar O. S. Sastry Renu Dahiya Manander Bangar Takumi Takashima 《International Journal of Green Energy》2016,13(6):580-584
The effect of air mass (AM) on the performance of multi-crystalline silicon (m-Si), amorphous silicon (a-Si), and hetero-junction with intrinsic thin layer (HIT)-technology-based photovoltaic (PV) modules are evaluated for representative day of four seasons during the year 2011 for composite climate of India. To find the best performing PV module technology with respect to AM at the site, annual energy yields and performance ratio against different AM bands (AM 1–4.5) are plotted. It is found that HIT modules perform better than m-Si and a-Si at each AM band. Annual energy yields for all three technologies decrease with increasing order of AM bands. The performance ratio for HIT and m-SI modules initially increases and then decreases with increasing order of AM bands. However, for a-Si modules, the performance ratio decreases with increasing order of the AM bands. 相似文献
3.
Iwanaga Takumi 《International Journal of Green Energy》2020,17(14):946-950
ABSTRACT Biodiesel emulsion fuel is reported as one of the most feasible options capable of generating lower NOx emission than that from fossil fuels. However, oil and water in the emulsion fuel are easily separated and unstable. The aim of the present study is to consider the production and stability of biodiesel emulsion fuel by using tetraglycerin ester (CR-310), i.e., one of lipophilic surfactant, polyglycerol polyricinoleate (PGPR) and biodiesel, i.e., Waste cooking Oil Methyl Ester (WOME) produced based on waste cooking oil. The corresponding heat rate, water content, and viscosity are measured. Emphasis is placed on the effects of water content and surfactant on biodiesel emulsions. It is found that: (i) stable emulsion fuel is obtained by adding at least 2.0% of CR-310 and is maintained over 1 month, (ii) there is no effect of water content on stable emulsion fuel if CR-310 is used over 2.0%, and (iii) the viscosity of emulsion fuels is higher than that of the biodiesel fuel and is gradually increased with an increase in the water content. 相似文献
4.
Teru Yamamoto Kazuo Higashino Tamae Abe Takumi Takasuga Hiroaki Takemori Roland Weber Yuko Sasaki 《Environmental science and pollution research international》2018,25(32):31874-31884
Studies on the formation of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) during the electrolysis of sodium chloride solution (brine) using graphite or titanium electrodes were carried out at a laboratory scale. High concentrations of PCDFs but no PCDDs were formed in tests using graphite electrodes. With titanium electrodes, PCDFs were only formed when tar pitch was added and mainly originated from the dibenzofuran present in the tar. For the first time, a detailed assessment of the formation of mono- to octachlorinated PCDD/PCDF from tar pitch was investigated. The assessment included of the chlorination steps proved that PCDFs were formed by successive lateral chlorinated from dibenzofuran to MonoCDFs, DiCDFs, and TriCDFs to form the typical known “chlorine pattern” of TetraCDF to OctaCDF with a dominance of 1,2,7,8- and 2,3,7,8-TetraCDFs, 1,2,3,7,8-PentaCDF, and 1,2,3,4,7,8-HexaCDF as marker congeners. The final homologue distributions depended on reaction time and reaction temperature. In addition, electrolysis with non-chlorinated dibenzo-p-dioxins, dibenzofuran, and biphenyl was carried out. As a result, PCDDs, PCDFs, and PCB were formed at comparable yields. Congener patterns in soil samples from a PCDD/F-contaminated site where chlor-alkali electrolysis had been operated for decades in Japan had identical isomer distribution demonstrating the source and contamination potential and risk of these processes. Therefore, sites where in the past 120 years chlor-alkali electrolysis has been operated or where residues from chlor-alkali production or other chlorine using industries have been disposed should be assessed for their pollution level and exposure relevance. The assessment of total organohalogen content revealed that PCDF is only a small fraction of organohalogens in the contaminated soils. For an appropriate risk assessment, also other chlorinated aromatic compounds such as PCBs or PCNs need to be considered. 相似文献
5.
All-solid-state Z-scheme photocatalysts, containing Cu2O, TiO2 (rutile), and Au as the electron mediator, were prepared and applied to the reduction of Cr(VI) in aqueous solutions. The Cu2O–Au–TiO2 composites were prepared by loading Au core–Cu2O shell hemisphere particles on TiO2 (rutile) nanorods using a two-step photocatalytic deposition process. Under ultraviolet–visible (UV–vis) light illumination, the Cu2O–Au–TiO2 composites exhibited higher photocatalytic Cr(VI) reduction activities than those exhibited by single TiO2 (rutile) and Cu2O. In this reaction, a precipitate containing Cr, which was considered to be Cr(OH)3, was deposited site-selectively on the Au core–Cu2O shell particles of the composites, indicating that the reduction site of the composite was Cu2O, and the reaction proceeded according to the Z-scheme. The Cu2O–Au–TiO2 composites also exhibited photocatalytic activity under visible light illumination. The oxidation state of Cu in the Cu2O–Au–TiO2 composite gradually changed from Cu(I) to Cu(II) during the photocatalytic Cr(VI) reduction. However the composite maintained its high photocatalytic performance even after oxidation. The role of Au in the Cu2O–Au–TiO2 composite was examined by comparing the properties of the Cu2O–Au–TiO2 composite with those of the Cu2O–TiO2 composite prepared via direct Cu2O deposition on TiO2. 相似文献
6.
Kurunthchalam Senthilkumar Naomasa Iseki Sunardi Seiichi Kasuga Takumi Takasuga Shigeki Masunaga 《毒物与环境化学》2013,95(4-6):121-132
Polychlorinated-dibenzo-p-dioxins (PCDDs), -dibenzofurans (PCDFs) and -dioxin-like polychlorinated biphenyls (DLPCBs) were determined in aquatic wildlife of Kasumigaura Lake (KUL), Japan from 1978 to 2001. Two plankton species elucidated several fold greater concentrations (2400–7800) than small tiger fish (310–6500), shrimp (160–1100), and three large fish namely, black bass (120–240), carp (94–120) and mullet (54) on pg/g fat. PCDD homologues were predominant accumulants with >68–<95% contribution and remaining was shared by PCDFs. Accumulation, non-ortho DLPCBs in plankton (3500–9200), shrimp (1600–8600) and small fish (2000–8800) and large fish (1300–3900) on ng/g fat basis were several orders magnitude greater than PCDD/DFs. The mono-ortho DLPCBs in large fish species were 23?000–83?000?ng/g fat and which it is accounted 94.3–95.9% the total dioxin-like PCBs accumulation. Temporal trends of PCDDs, PCDFs, non-ortho PCBs and TEQ in shrimp and small tiger fish were varied. The mullet had minimum toxic equivalency “TEQ” (14?pg?TEQ/g) followed by plankton Neomysis intermedia (25?pg?TEQ/g), small tiger fish (mean: 33, ranges 14–66?pg?TEQ/g), plankton Cyclopus vicinus (34?pg?TEQ/g), carp (mean: 35, ranges 32–38?pg?TEQ/g), shrimp (mean: 38, ranges 11–68?pg?TEQ/g) and black bass (mean: 59, ranges 38–79?pg?TEQ/g) on fat basis. In all the samples, PCDD was predominant TEQ contributor followed by PCDFs and DLPCBs. The contribution of mono-ortho DLPCBs to the total TEQ was 0.52–0.92 in large fish. 相似文献
7.
Anna Kärrman Kouji H. Harada Kayoko Inoue Takumi Takasuga Etsumasa Ohi Akio Koizumi 《Environment international》2009,35(4):712-717
Daily dietary intake of perfluorinated chemicals (PFCs) in relation to serum levels was assessed by determination of nine PFCs including perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) in matched daily diet duplicates and serum samples. Diet and serum were collected in year 2004 from 20 women in Osaka and Miyagi, Japan. Only PFOS and PFOA were detected in the diet samples and no significant difference between cities was seen. After adjusted by water content, diet concentration of PFOA was significantly higher in Osaka. The median daily intake calculated using the measured diet concentrations was 1.47 ng PFOS/kg b.w. and 1.28 ng PFOA/kg b.w. for Osaka, and 1.08 ng PFOS/kg b.w. and 0.72 ng PFOA/kg b.w. for Miyagi. A significant difference between cities was seen for the serum concentrations with median of 31 ng/mL PFOS and PFOA in Osaka, compared to 14 ng/mL PFOS and 4.6 ng/mL PFOA in Miyagi. Carboxylates such as perfluorononanoic acid (PFNA) and perfluoroundecanoic acid (PFUnDA) were also detected in serum at median levels 6.9 ng/mL and 3.2 ng/mL (Osaka), and 2.8 ng/mL and 5.1 ng/mL (Miyagi). Based on one-compartment model under steady state, dietary intake of PFOS and PFOA accounted for only 22.4% and 23.7% of serum levels in Osaka females, and in contrast 92.5% and 110.6% in Miyagi females, respectively. 相似文献
8.
采用等离子体协同改性凹凸棒石催化脱除NOx,研究了等离子体反应器输入电压和凹凸棒石煅烧温度对NO和NOx脱除率的影响规律.结果表明,当反应器输入电压30kV时,NO和NOx脱除率随等离子体输入电压增加而增大.凹凸棒石煅烧温度对催化活性也具有显著影响,当煅烧温度600℃时,部分凹凸棒石被烧结熔融, NO和NOx脱除率都不高;当煅烧温度为400~600℃时,凹凸棒石活性较高, NO和NOx脱除率可达最大值.本实验条件下最佳工艺参数为等离子体输入电压>30kV, 凹凸棒石煅烧温度为400~600℃,NOx最大脱除率可达89.6%. 相似文献
9.
Senthil Kumar K Bowerman WW DeVault TL Takasuga T Rhodes OE Lehr Brisbin I Masunaga S 《Chemosphere》2003,53(2):173-182
Blood of adult and juvenile black and turkey vultures in the Savannah River Site of South Carolina, USA was analyzed for the presence of 2,3,7,8-chlorine substituted polychlorinated dibenzo-p-dioxins (2,3,7,8-PCDDs), dibenzofurans (2,3,7,8-PCDFs), -dioxin-like and -di-ortho polychlorinated biphenyls. Concentration ranges of 2,3,7,8-PCDD/DFs in blood of black and turkey vultures were 14.2-34.6 and 8.7-56.2 pg/ml wet wt., respectively. Dioxin-like PCBs were in the ranges of 815-4627 and 753-3611 pg/ml wet wt. respectively, in black and turkey vultures. Considerable concentrations of two congeners of di-ortho PCBs were noticed in the ranges of 1415-10325 and 663-7500 pg/ml respectively, in black and turkey vultures. Comparatively, greater toxic equivalency (TEQ) were observed in blood of turkey vultures with the ranges of 3.2-20, whereas black vulture contained 1.8-8.4 pgTEQ/ml wet wt. basis. The species-specific accumulation profiles of PCDD/DFs and dioxin-like PCBs may reflect the different feeding habits, ecology, metabolic capacity and migratory movements of these two scavenging species. 相似文献
10.
Speciments of the red frog crab, Ranina ranina, examined in this study were collected off Hachijojima, Japan from 1987–1988 and 1990–1991. Ovigerous females occurred from May to September, and their carapace length ranged from 61.8 to 102.1 mm. Minimum size at the maturity was estimated to be 50 to 60 mm carapace length. The lobule-type ovary had a longitudinal ovarian cavity at the center. Germinal zones were located along the sides of the cavity. Oogenesis was divided into five main and ten detailed stages: proliferation (oogonium); previtellogenesis (bouquet, early chromatin nucleolus, late chromatin nucleolus); primary vitellogenesis (oil globule and yolk granule); secondary vitellogenesis (primary yolk platelet, secondary yolk platelet and prematuration); and maturation (maturation) stages. Vitellogenesis started at the oil globule stage when weakly positive periodic acid-Schiff granules appear in the cytoplasm. Based on the gonadosomatic index and histological changes in ovary, the reproductive cycle was divided into five stages: multiplication, from December to January; developing, from February to March; ripe in April and early May; spawning, from late May to August; and recovery, from August to November. Each crab spawned more than once during the spawning season. 相似文献