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树脂吸附法处理对硝基酚钠废水的研究 总被引:7,自引:0,他引:7
本文研完了H—103吸附树脂处理对硝基苯乙醚生产过程中产生的含对硝基酚钠废水的最佳工艺条件。实验结果表明,H—103树脂的吸附率达99.9%以上。工作吸附量150~200mg/l,以工业酒精作脱附剂,脱附率达95%以上,对硝基酚钠的回收率达90%,经处理后的废水可达到排放标准,回收的对硝基酚钠质量较好,可作为化工原料用于生产。 相似文献
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树脂吸附法处理DCP生产过程中混合含酚废水的研究 总被引:4,自引:1,他引:3
本文选用南开牌NKA吸附树脂对过氧化二异丙苯(简称DCP)生产过程中的混合含酚废水进行处理,较系统地研究了废水的予处理方法和废水的pH值、浓度、温度、流速以及脱附剂的类型、浓度、流速等对NKA树脂的吸附——脱附性能的影响,并取得了满意的效果。当废水酚含量为1000~2000ppm时,NKA树脂的工作吸附量为50mg/ml左右,吸附率约达100%,以工业酒精为洗脱剂的洗脱率达95%,经处理后的废水酚浓度小于0.5ppm,一次可处理废水30~50BV。 相似文献
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树脂吸附法处理异丙隆生产过程中含异丙隆废水的研究 总被引:3,自引:0,他引:3
本文用CHA—101树脂处理异丙隆生产过程中的含异丙隆废水,控制泄漏点在异丙隆浓度为140mg/l时,树脂可处理废水36BV,树脂工作吸附量约70mg/ml,树脂的吸附率达95%,吸附后废水经试验可完全套用到生产异丙隆工段中去,实现了闭路循环。树脂吸附饱和后,用工业酒精能基本脱附异丙隆。 相似文献
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以大孔吸附树脂对含对硝基苯胺工业废水进行了治理研究。结果表明,CHA-101大孔吸附树脂对该废水的吸附处理效果良好,处理后废水中对硝基苯胺含量可降低至3mg/L以下,去除率达99%以上;树脂脱附再生的同时可回收对硝基苯胺。 相似文献
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将树脂吸附剂应用于焦化废水的深度处理,考察了温度、投加量、初始pH、时间和流速对CODcr和色度去除效果的影响.静态吸附实验确定了最佳吸附树脂为NDA-99型树脂,最佳投加量为3.00g/L,无需调节pH,最佳温度为303K,吸附等温线满足Freundlich方程.通过动态实验确定了最适宜工艺条件为:流速20BV/h,单柱废水处理量为200BV/批;处理后废水中CODcr浓度从199mg/L降到100mg/L以下,色度从98倍降到50倍以下.使用8%的NaOH溶液脱附再生,最佳脱附流速为5BV/h. 相似文献
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树脂吸附法处理五氯酚钠生产废水 总被引:18,自引:2,他引:18
本文用大孔吸附树脂CHA—111处理五氯酚钠(PCP—Na)生产废水,其中PCP—Na含量为10000~15000mg/L,CODcr高达11000mg/L。经中和沉淀-树脂吸附法处理,处理量为12BV,吸附流出液中五氯酚(PCP)含量≤1.1mg/L,PCP去除率>99%,CODcr总去除率≥80%,树脂脱附液经酸化处理,可回收PCP。 相似文献
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Uroš Grošelj Mojca Žorž Amalija Golobič Branko Stanovnik Jurij Svete 《Tetrahedron》2013,69(52):11092-11108
A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives. 相似文献
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The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp3)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp2)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp2)?H and aliphatic 1,5- and 1,6-C(sp3)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp3)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp2)?H insertion. 相似文献
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N-Heterocyclic carbene-palladacyclic complexes 3 were successfully achieved in a one-pot procedure under mild conditions. The structure of 3a was unambiguously confirmed by X-ray single crystal diffraction and it was an active catalyst in the Buchwald-Hartwig amination and α-arylation of ketones even at very low catalyst loadings (0.01?mol%). 相似文献
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Shashikant U. Dighe Surya K. Samanta Shivalinga Kolle Sanjay Batra 《Tetrahedron》2017,73(17):2455-2467
An efficient iodine-mediated oxidative Pictet-Spengler reaction in dimethyl sulphoxide (DMSO) using terminal alkynes as the 2-oxoaldehyde surrogate for the synthesis of aryl (9H-pyrido[3,4-b]indol-1-yl)methanones is described. The scope of the protocol includes the total synthesis of Fascaplysin, Eudistomins Y1 and Y2. The methodology is extended for preparing pyrrolo[1,2-a]-quinoxaline and indolo[1,5-a]quinoxaline derivatives. The utility of 1-aroyl-β-carbolines was demonstrated by performing palladium-catalyzed β-carboline directed ortho-C(sp2)-H functionalization of the phenyl ring with thiomethyl (SMe) group using DMSO as source and for accessing 4-aryl-canthin-6-ones. 相似文献
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In this Letter, we described a facile method for constructing fused bicyclic 1-arylpyrazol-5-one ring system. We employed various methylene-containing carboxylic acids as the substrates and proved that the pyrazolone ring closure requires activated methylene group in intermediate II. Accordingly, a series of structurally diversified, fused bicyclic 1-arylpyrazol-5-ones was prepared in moderate to high yields using the requisite substrates. 相似文献
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Synthesis of substituted pyrrolo[1,2-a]pyrazines and pyrazino[1,2-a]indoles from the Morita-Baylis-Hillman derivatives of acrylates via saponification followed by Curtius reaction is described. 相似文献
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用正丁胺作为碳源,采用射频辉光放电制备碳膜,选用激光染料R6G和聚乙二醇混合液作为蒸气源,采用单源热蒸发,在蒸发室与染料同时沉积得到混合膜,用拉曼光谱和红外光谱分析了碳膜的结构和键合方式,分析表明:碳膜中存在胺基团和氢原子.混合膜的荧光谱测量结果表明,认为正丁胺对染料荧光谱的影响是因为胺基和氢原子的存在. 相似文献
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Jona Mirnik Eva Pušavec Kirar Sebastijan Ričko Uroš Grošelj Amalija Golobič Franc Požgan Bogdan Štefane Jurij Svete 《Tetrahedron》2017,73(24):3329-3337
A series of 20 CuAIAC reactions between eight 4-acylamino substituted pyrazolidine-3-one-1-azomethine imines and four terminal ynones were performed using Cu0 as catalyst. The corresponding fluorescent cycloadducts were obtained in very high yields upon simple workup. Thus, Cu-metal turned out to be a better catalyst than CuI in terms of yield and ease of isolation. Availability of azomethine imines, mild reaction conditions, and simple workup enable a “click” access to libraries of densely substituted 2,3-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-ones. Reactivity of differently substituted dipoles was evaluated experimentally and by quantum chemical methods (DFT). 相似文献
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George E. Magoulas Thomas Garnelis Constantinos M. Athanassopoulos Dionissios Papaioannou George Mattheolabakis Konstantinos Avgoustakis Dimitra Hadjipavlou-Litina 《Tetrahedron》2012,68(35):7041-7049
(E)-4-(Fullerenopyrrolidin-1-yl)-3-methylbut-2-enoic acid and its corresponding succinimidyl ester, readily obtained through Prato-type modification of C60, were used for the selective N-acylation of polyamines. The thus obtained conjugates were evaluated for their antioxidative and anti-inflammatory activity and their cytotoxicity was determined. Members of this family of compounds showed interesting anti-lipid peroxidation, anti-lipoxygenase and anti-inflammatory activity and comparable cytocompatibility to spermidine. 相似文献