羧甲基壳聚糖对染料废水的脱色研究

纺织工业是我国重要的经济部门,也是我国工业废水的排放大户,其中印染废水排放量又占纺织工业废水排放量的80%,已成为我国各大水域的重要污染源。印染废水的两大污染指标是色度和COD,污染的特点和处理的难点是色度高,脱色困难[1-2]。作为一种天然生物高分子,壳聚糖(chitosan,简称CTS)以其独有的絮凝、成膜、吸附、螯合等性能在印染废水脱色研究领域得到广泛应用[3-8]。作为絮凝剂处理废水时,壳聚糖由于水溶性差而需先溶于稀酸,应用受到一定限制,故人们纷纷将其改性制成水溶性的羧甲基壳聚糖(carboxy-methyt chitosan,简称NOCC)。张秋华[…     

GRS大红和弱酸红R混合液的光催化降解模拟研究

近年来,利用半导体材料处理印染废水的光催化氧化技术研究日益受到重视.该技术与传统的污水处理方法相比,具有高效、稳定、无二次污染以及对各类有机污染物(包括难生物降解的有毒污染物)可深度、彻底氧化等突出优点[1-2].目前对该技术研究的关注焦点放在高催化活性的光催化剂的研制上,但近年已有人开始利用已有催化剂如TiO2对印染废水进行光催化降解模拟研究,分析确定降解影响因素,并研究降解条件的优化,从而为该技术的应用奠定基础[3-5].     

一种复合脱色剂在印染废水中的应用研究

以甲醛、双氰胺、醋酸钠、氯化铵、氯化铝等为原料制备了一种印染废水脱色絮凝剂T-1。采用福州某纺织印染有限公司的印染废水为处理对象,以脱色率为主要考核指标,讨论了T-1的投加量、pH值、废水温度等对絮凝效果的影响。实验结果表明,双氰胺-甲醛缩聚物对印染废水具有优良的脱色絮凝效果,当投加量为100mg/L,废水温度为30℃,pH=8时,处理效果最佳,色度去除率达70%,COD去除率为78.3%。而且其絮凝性能明显优于聚合氯化铝(PAC)、聚合硫酸铝(PAS)絮凝剂。     

UV/TiO_2降解丽华实军蓝制衣染料的研究

<正>印染废水是目前主要的难处理的有害工业废水之一[1]。近十几年发展起来的TiO2光催化氧化水处理技术,以其具有光催化活性高、降解彻底、非选择性、无二次污染、常温常压操作、能耗及材料消耗低且TiO2耐酸碱和耐光化学腐蚀、无毒等优点为解决这一难题提供了一种有效的方法,在印染废水处理中受到了广泛关注[2～6]。     

印染废水的植物修复及在线监测技术研究

采用空心莲子草对印染废水进行修复,研究净化效果,并利用在线监测技术对植物修复前后的印染废水中氨氮、COD、TOC指标进行测定。结果表明：在线监测技术成熟,植物修复印染废水可行。     

絮凝-漂白粉催化氧化处理印染废水

采用絮凝-漂白粉催化氧化法,筛选出硫酸镁催化剂,提高难生化处理的印染废水对色度、COD的去除效果。实验结果表明,对COD_(Cr) 592 mg/L、色度625倍、pH 9.82、SS 150 mg/L的某印染废水,当废水p H为6时,投加Al_2(SO_4)_3·18H_2O 400 mg/L、聚丙烯酰胺(PAM)2 mg/L,催化剂硫酸镁80 mg/L,有效氯30%的漂白粉1.0 g/L,CODCr最终去除率达到88.2%,色度去除率98.4%,浊度去除率86.6%,出水pH为6,达到国家二级排放标准。催化氧化的脱色速率提高近一倍,结果对印染废水的处理研究和实际应用具有一定价值。     

复合型高效絮凝脱色剂处理印染废水的研究

选用自制的双氰胺甲醛作为絮凝脱色剂处理高浓度印染废水,并与硫酸铝、三氯化铝作了对比实验。考察了投加量、pH值、反应温度等因素对絮凝效果的影响。实验结果表明在用量较少并且其它操作条件相同的情况下,双氰胺甲醛制备的脱色絮凝剂具有很好的絮凝脱色效果及COD_(Cr)去除率。在最佳的操作条件下(投加量120 mg/L,pH=7,反应温度25℃),此脱色絮凝剂对分散、酸性、活性印染废水的COD_(Cr)去除率分别为79.1%、78.5%、79.0%,对分散、酸性、活性印染废水的脱色率分别为94.0%、97.1%、72.9%,减轻了后续处理难度。在与无机絮凝剂的对比试验中,在相同的条件下有机絮凝剂的处理效果总体比无机絮凝剂的处理效果好。     

二氧化钛纳米微粒的制备及对染料橙黄Ⅱ的光催化氧化

染料废水的处理是受人关注的重要课题之一。而水溶性偶氮染料是印染工业中污染治理的主要对象,由于其色度深,浊度大,分子结构相对稳定,用传统的方法进行处理效果不佳,而近年来发展起来的半导体光催化氧化技术,为人们提供了一种有效的方法[1-3],在常见的半导体光催化剂中,TiO2以     

聚合氯化铝铁与磷酸氢二钠复合絮凝剂的制备及其对印染废水的处理

利用正交试验方法对印染废水的混凝处理最佳试验条件进行了研究。通过聚合氯化铝铁(PAFC)和磷酸氢二钠(NaH2PO4·2H2O)对模拟印染废水处理效果的研究表明,在溶液pH为7、PAFC与NaH2PO4·2H2O投加量比为3∶2、温度为55℃、搅拌时间为15min时,对模拟印染废水处理得到较为满意的效果,COD的去除率为80.45%,经处理后水的吸光度为0.4269。     

印染废水的电化学深度处理及回用研究

针对印染废水水质特性,在PbO₂/Ti阳极、不锈钢板阴极的电解反应器中研究了电化学氧化对印染废水生化出水的处理效果. 试验结果表明,电氧化工艺可以实现化学需氧量（Chemical Oxygen Demand,COD）、氨氮和色度的同步去除. 在电流密度10 mA·cm^-2时电解60 min,废水中COD、氨氮、色度、氯离子浓度以及pH值等指标均可达到GB/T 19923-2005《城市污水再生利用工业用水水质》中工艺与产品用水标准,电流效率达45.6%,吨水能耗4.1 kW·h.     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

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%.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

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.     

Highly regioselective Buchwald–Hartwig amination at C-2 of 2,4-dichloropyridine enabling a novel approach to 2,4-bisanilinopyridine (BAPyd) libraries

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.     

Sulfur-directed metal-free and regiospecific methyl C(sp3)–H imidation of thioanisoles

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.     

Selective syntheses of 2H-1,3-oxazines and 1H-pyrrol-3(2H)-ones via temperature-dependent Rh(II)-carbenoid-mediated 2H-azirine-ring expansion

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.     

Copper catalyzed/mediated synthetic methodology for ebselen and related isoselenazolones

Scope of the copper catalyzed/mediated selenium-nitrogen coupling reaction has been studied for the synthesis of isoselenazolones. It is noticed that the 2-chloro, 2-bromo-, and 2-iodo-aryl amides substrates can be exploited in the selenium-nitrogen coupling reaction by employing 25-100 mol % of CuI/1,10-phenanthroline (L) and potassium carbonate as a base in DMF. Furthermore, electron rich 2-chloro-arylamides also underwent selenium-nitrogen coupling reaction to give biologically important selenium-nitrogen heterocycles. Also, copper-catalyzed selenium-nitrogen coupling reaction has been meticulously applied for the synthesis of diaryl diselenides having methoxy, amine, and amide functionality from respective aryl iodides in the presence of stoichiometric amount of succinimide as an external Se-N coupling partner.     

Knoevenagel condensation catalyzed by novel Nmm-based ionic liquids in water

A series of novel N-methyl morpholine (Nmm) based ionic liquids with 1,2-propanediol group were synthesized and used as catalysts for Knoevenagel condensation at room temperature in water. Under the effect of the catalyst, various aldehydes or aliphatic ketones could react with a wide range of activated methylene compounds well, including malononitrile, alkyl cyanoacetate, cyanoacetamide, β-diketone, barbituric acid, 2-arylacetonitrile and thiazolidinedione. Furthermore, most of the products could be separated just by filtrating and washing with water. Additionally, the catalyst is recyclable and applicable for the large-scale synthesis.     

Construction of polyheterocyclic spirotetrahydrothiophene derivatives via sulfa-Michael/aldol cascade reaction

A series of polyheterocyclic spirotetrahydrothiophene derivatives were obtained in moderate to excellent yields via a catalyst-free sulfa-Michael/aldol cascade reaction of chalcones 1 and commercially available 1,4-dithiane-2,5-diol 2 under mild conditions. We also present the first asymmetric sulfa-Michael/aldol cascade reaction of chalcones 1 and commercially available 1,4-dithiane-2,5-diol 2 with moderate to good enantioselectivities catalyzed by readily available chiral phase-transfer catalysts (PTCs).     

Suzuki-Miyaura reactions of the soluble guanylate cyclase inhibitor NS2028: a non-product specific route to C-8 substituted analogues

Both soluble guanylate cyclase (sGC) inhibitors ODQ 1 and NS2028 2 are synthesized via improved protocols. In the former case treating 3,4-dihydroquinoxalin-2(1H)-one oxime 8, which can be prepared in two steps from 1,2-benzenediamine, with 1,1′-carbonyldiimidazole (CDI) gives the dihydro-ODQ 10 that in the presence of KMnO₄ oxidises to give ODQ 1 in an overall yield of 46% starting from 1,2-benzenediamine. In the latter case, the synthesis affords NS2028 2 from 2-amino-4-bromophenol 3 in three steps with an overall yield of 85% and avoids the need for chromatography. Furthermore, Suzuki-Miyaura reaction conditions are described that enable the preparation of 8-aryl and 8-heteroaryl derivatives of NS2028 directly from NS2028 2. Finally, demethylation of the 8-(methoxyphenyl) substituted analogues afforded the 8-(hydroxyphenyl) derivatives 40-42. All new products are fully characterised.