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1.
采用厌氧——缺氧——SBR微生物生化处理组合工艺,研究了双基(含双基混合酯)球扁药含氮废水处理技术,通过菌种驯化,实现了高盐浓度、高CODCr含量废水经处理后达标排放,CODCr的总去除率达到97.7%,质量浓度降到96mg/L;BOD5总去除率达到了98.O%,质量浓度降到28mg/L;SS的总去除率达到94.4%,质量浓度降到了9mg/L。 相似文献
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用Fenton-UASB-生物接触氧化组合工艺对Fischer-Tropsch合成废水进行处理。实验结果表明,采用Fenton法对废水进行预处理,在pH值为3,H2O2的投加量为30 mL/L,Fe2+投加量为1.2 g/L,反应时间为120 min时,去除了63%的CODCr,有效地提高了废水的可生化性;Fenton预处理出水经UASB厌氧生物处理后,CODCr去除率达90%以上;最后经接触氧化后,出水CODCr达100 mg/L以下,达到了GB8978-1996《污水综合排放标准》中化工类废水的二级排放标准。 相似文献
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Ti/Sb2O5-SnO2/PbO2电极电催化氧化对氨基苯酚 总被引:2,自引:0,他引:2
以电沉积法制备的Ti/Sb2O5-SnO2/PbO2电极作阳极,恒电流电解水溶液中的对氨基苯酚(PAP),利用紫外光谱探讨了对氨基苯酚电催化氧化的反应历程,系统地考察了电解时间、反应温度,pH值、电流密度以及对氨基苯酚初始浓度对COD去除率的影响,提出了电催化氧化对氨基苯酚的最佳条件.结果表明,对氨基苯酚电催化反应为逐级氧化历程,主要中间产物为苯醌、丁烯二酸和草酸,最终产物为CO2和水.20℃,对初始浓度10mg/L的对氨基苯酚水溶液(pH=6),恒定电流密度100mA/cm^2,电解1h,COD去除率可达98.5%.该方法作为废水中对氨基苯酚的最小化处理.具有良好的应用前景. 相似文献
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树脂吸附法处理水杨酸甲酯生产废水的研究 总被引:7,自引:0,他引:7
采用吸附树脂NDA—99处理水杨酸甲酯生产废水,结果表明该树脂时废水中的5磺基水杨酸及水杨酸均具有良好的吸附—脱附性能.废水经预处理和吸附处理后,CODCr由57000-59000mg/L降至6300mg/L左右,去除率接近89%.用IBV8%NaOH 3BVH2O作脱附剂,在温度为60℃、流量为IBV/h的条件下,脱附率接近100%,树脂可重复使用.高浓度脱附液经酸化、浓缩、冷却结晶,可回收5—磺基水杨酸,回收率为95%左右。纯度为78%。 相似文献
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采用热氧化法制备Ti/RuO_2-CoO电极,通过SEM和XRD对电极涂层的表面形貌和晶体结构进行表征;并利用最佳条件制备的电极开展电化学氧化氨氮模拟废水研究。实验研究了电流密度、初始pH值、Cl~-浓度和NH_3-N初始浓度对NH_3-N降解效果的影响。研究结果表明:当n(Ru)/n(Co)=7∶3时Ti/RuO_2-CoO电极对NH_3-N的去除效果较好。随着电流密度的增加,NH_3-N去除率随之升高;初始pH为碱性条件时,NH_3-N去除效果较好;NH_3-N去除率随Cl~-浓度的增加呈现先增大后减小,当Cl~-浓度为3 000 mg/L时,氨氮去除率达到97.95%。当电流密度为70 mA/cm~2、Cl~-浓度为3 000 mg/L、初始pH=9时,经过180 min电解后,氨氮初始浓度从500 mg/L降低至10.25 mg/L,且电化学氧化氨氮的产物主要为氮气和硝酸盐氮。 相似文献
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镀铜铁屑-H_2O_2催化氧化降解含酚废水 总被引:2,自引:0,他引:2
采用镀铜铁屑代替传统Fenton体系中的FeSO4作为催化剂,通过改变H2O2与镀铜铁屑的投加量、溶液的pH值、反应温度、反应时间等条件,研究了该体系对处理苯酚废水的影响。结果表明,常温下处理实际含酚印染废水,在pH值为4~6,30%H2O2 12mL/L,镀铜铁屑5g/L,反应时间为45min时,COD去除率可达96%,其CODCr从5827mg/L降至419mg/L,色度从2000降至30,符合国家三级排放标准。 相似文献
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用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%. 相似文献
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Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction
Laurent Gavara Thomas Boisse Jean-Pierre Hénichart Adam Daïch Philippe Gautret 《Tetrahedron》2010,66(38):7544-5571
In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments. 相似文献
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The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula. 相似文献
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Rebecca J. Burton Mandy L. CrowtherNeal J. Fazakerley Shaun M. FilleryBarry M. Hayter Jason G. KettleCaroline A. McMillan Paula PerkinsPeter Robins Peter M. SmithEmma J. Williams Gail L. Wrigley 《Tetrahedron letters》2013
The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines. 相似文献
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KMnO4-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields. 相似文献
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N. A. Nedolya 《Chemistry of Heterocyclic Compounds》2008,44(10):1165-1219
The review contains a concise historical account and information on the most significant researches undertaken by the staff
at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry
of Heterocyclic Compounds.
Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008. 相似文献
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Regiospecific and direct imidation of the methyl C(sp3)–H bond of thioanisoles is realized under mild and metal-free conditions with N-fluorobis(benzenesulfonyl)imide as an oxidant and nitrogen source. Proposed mechanism suggests that thionium ion intermediates and a Pummerer-type reaction are involved. The imidation has advantages such as high step-economy, excellent functionality tolerance, and regiospecificity, giving structurally diverse imidation products. 相似文献
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《Tetrahedron》2014,70(21):3377-3384
The Rh(II)-catalyzed reaction of 2-carbonyl-substituted 2H-azirines with ethyl 2-cyano-2-diazoacetate or 2-diazo-3,3,3-trifluoropropionate provides an easy access to 2H-1,3-oxazines and 1H-pyrrol-3(2H)-ones. These compounds can be selectively prepared from the same starting material using temperature as the only varied parameter. The 2-azabuta-1,3-diene intermediate, a common precursor for both heterocyclic products, isomerizes into 2H-1,3-oxazine under kinetic control, while 1H-pyrrol-3(2H)-one is the sole product of the reaction at elevated temperatures. According to DFT-calculations a one-atom oxazine ring contraction involving ring-opening to a 2-azabuta-1,3-diene intermediate, followed by a 1,5- and 1,2-prototropic shift leads to the consecutive formation of imidoylketene and azomethine ylide, which then further undergo cyclization to the pyrrole derivative. 相似文献
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Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields. 相似文献