现代农业科技
現代農業科技
현대농업과기
XIANDAIHUA NONGYE
2015年
8期
223-224,226
,共3页
康可佳%刘侨博%刘薇%曾红云%曲茉莉
康可佳%劉僑博%劉薇%曾紅雲%麯茉莉
강가가%류교박%류미%증홍운%곡말리
罗丹明B%电芬顿%印染废水
囉丹明B%電芬頓%印染廢水
라단명B%전분돈%인염폐수
rhodamine B%electrolysis fenton process%dyeing wastewater
为考察电芬顿降解罗丹明B的机制,对初始pH值、温度、亚铁浓度的反应动力学进行研究。为测定最佳条件下过氧化氢的含量、羟基自由基的相对含量及罗丹明B随时间的降解产物,开展UV-vis及GC-MS研究。经GC-MS分析,检测出了12种物质,分别为已二酸、丙二酸、丁二酸、领苯二甲酸酐、苯甲氧基胺、乙二醇、2-羟基苯甲酸、苯甲酸、2-羟基戊二酸、邻苯二甲酸、间苯二甲酸、对苯二甲酸,分别提出了可能的降解机制。在最佳条件下,50 min后溶液中的过氧化氢含量为6 mmol/L,过氧化氢与羟基自由基的相对含量变化趋势相同。
為攷察電芬頓降解囉丹明B的機製,對初始pH值、溫度、亞鐵濃度的反應動力學進行研究。為測定最佳條件下過氧化氫的含量、羥基自由基的相對含量及囉丹明B隨時間的降解產物,開展UV-vis及GC-MS研究。經GC-MS分析,檢測齣瞭12種物質,分彆為已二痠、丙二痠、丁二痠、領苯二甲痠酐、苯甲氧基胺、乙二醇、2-羥基苯甲痠、苯甲痠、2-羥基戊二痠、鄰苯二甲痠、間苯二甲痠、對苯二甲痠,分彆提齣瞭可能的降解機製。在最佳條件下,50 min後溶液中的過氧化氫含量為6 mmol/L,過氧化氫與羥基自由基的相對含量變化趨勢相同。
위고찰전분돈강해라단명B적궤제,대초시pH치、온도、아철농도적반응동역학진행연구。위측정최가조건하과양화경적함량、간기자유기적상대함량급라단명B수시간적강해산물,개전UV-vis급GC-MS연구。경GC-MS분석,검측출료12충물질,분별위이이산、병이산、정이산、령분이갑산항、분갑양기알、을이순、2-간기분갑산、분갑산、2-간기무이산、린분이갑산、간분이갑산、대분이갑산,분별제출료가능적강해궤제。재최가조건하,50 min후용액중적과양화경함량위6 mmol/L,과양화경여간기자유기적상대함량변화추세상동。
In order to study the degradation mechanism of rhodamine B by electro-fenton,reaction kinetics was studied in different initial pH value,temperature,concentration of Fe2+. Overall,the degradation followed the first-order reaction. In order to investigate the degradation mechanism of rhodamine B,the GC-MS and UV-vis technologies were applied. The amount of hydrogen peroxide and the relative amount of hydroxyl radicals were determined to get a better understanding of it. From GC-MS analysis,12 kinds of degradation products were detected. They were diacid,malonic acid,succinic acid,led the dimethyl anhydride,methoxy benzene amine,ethylene glycol,2-hydroxy benzoic acid,benzoic acid,2-hydroxy glutaric acid,phthalic acid,isophthalic acid,terephthalic acid. On this basis,possible degradation mechanism was proposed.Under optimal conditions,after 50 min,the hydrogen peroxide content was 6 mmol/L,the relative amounts of hydrogen peroxide and hydroxyl radicals had the same trends.