Removal of fulvic acid from aqueous media by adsorption onto modified vermiculite

Clay minerals are low cost materials that can be structurally modified and exploited for removal of natural organic matter from freshwaters. The present study shows that vermiculites modified by ion exchange with hexadecyltrimethylammonium or intercalation with poly(hydroxy iron) cations are potential adsorbents for removal of fulvic acid, whereas the adsorption on the raw clay mineral is negligible. The efficiency of the modified vermiculite was evaluated by measuring adsorption isotherms by the batch technique using initial fulvic acid concentrations between 2.5 and 50.0 mg L^− 1, with one hour of contact time. At least 94% of the fulvic acid initially present in a 20 mg L^− 1 solution was sorbed onto either the intercalated poly(hydroxy iron) cations or the organically modified vermiculite. Up to an initial concentration of 5.0 mg L^− 1 the adsorption is irreversible, and no quantifiable fulvic acid was measured in the desorption experiments. For initial fulvic acid concentrations between 10.0 and 50.0 mg L^− 1, desorption was between 2.3% and 4.9% for Fe(III) intercalated vermiculite, and between 1.4% and 9.2% for the organoclay. The adsorption percentages on intercalated poly(hydroxy iron) cations increased upon lowering pH and increasing the ionic strength, indicating the occurrence of strong binding mechanisms such as ligand exchange. Adsorption percentage of fulvic acid onto the organoclay also increased with lowering of pH, but in this case the adsorption percentages showed a small decrease at high ionic strength, suggesting that electrostatic attraction plays an important role in the adsorption process.     

In situ polycondensation of amino acid modified liposomes and their properties

Three amphiphilic amino acids based on glutamic acid, i.e. S-[1-carboxy-2-([N-bistetradecyl- -glutamate]carbon-yl)ethyl]cysteine (1), S-[1-carboxy-2-([N-bishexadecyl- -glutamate]carbonyl)ethyl]cysteine (2), S-[1-carboxy-2-([N-bis-octadecyl- -glutamate]carbonyl)ethyl]cysteine (3), were synthesized. The aggregation behavior of them in water or buffer solution was studied. It was found that upon hydration and sonication in water, they could form stable liposomes. This kind of amino acid modified liposome was then polycondensed locally on the liposome surface to form a polypeptide-surfaced liposome and the peptide formation was detected by Fr-IR, GPC, etc. The effect of polycondensation of amino acid on the properties of liposomes were studied by detecting the phase transition temperatures with DSC or measuring the leakage of the encapsulated fluorescent probe from the liposomes. It was observed that the phase transition temperatures of the peptide liposomes moved down and the polycondensation of amino acid moieties obviously increased the leakage of the encapsulated molecules.     

微波辐射对甲苯磺酸催化合成乙酸环己酯

以冰醋酸和环己醇为原料 ,环已烷为带水剂 ,对甲苯磺酸作催化剂 ,采用微波辐射技术 ,在常压下直接合成乙酸环己酯。最适宜反应条件为 :n(环己醇 )∶n(乙酸 ) =1 5∶1 0 ,对甲苯磺酸用量 0 2 0 g ,带水剂用量 5mL ,微波功率 5 95W ,辐射时间 15min ,产率达 97%以上     

焦化废水催化氧化处理的工艺条件实验

利用芬顿(Fenton)试剂的催化氧化性对焦化废水进行初步的处理,使其CODcr值除去率达80%以上,再用活性炭进行深度处理,使其CODcr值<40mg·L-1,总除去率达98%以上.     

2-羟基-3-烯丙氧基丙磺酸钠的合成

采用新方法合成了2-羟基-3-烯丙氧基丙磺酸钠。先由环氧氯丙烷和亚硫酸氢钠合成中间体3-氯-2-羟基丙磺酸钠，然后中间体再与丙烯醇在氢氧化钠催化下生成目标产物2-羟基-3-烯丙氧基丙磺酸钠。2步反应总收率在70％左右，中间体和产物分别进行了光谱表征。     

菲酐-纳米金修饰电极同时检测抗坏血酸、多巴胺和尿酸的研究

多孔结构的3,4,9,10-茈四甲酸二酐（PTCDA）作为骨架,用抗坏血酸做还原剂制备纳米金（GNPs）,制备了高催化活性的PrC—GNPs复合纳米材料。将该材料用于玻碳电极的修饰（GCE）,制得PTC—GNPs复合材料修饰的电极（PTC—GNPs／GCE）。该修饰电极能够同时对尿酸（UA）、多巴胺（DA）和抗坏血酸（AA）进行检测。分别使用循环伏安法（CV）和差分脉冲伏安法（DPV）对UA、DA和AA和在修饰电极上的电化学行为进行研究。实验结果表明,在pH=5．0的PBS缓冲体系中,该修饰电极对UA、DA和AA的线性响应范围分别为0．002～0．462mol／L、0．002～0．352mol／L和0．04～1．54mol／L。该传感在临床医学检测领域具有一定的应用前景。     

含有腐植酸的吸水性树脂在溶液及土壤环境中的性质研究

考察了含有腐植酸的吸水性树脂(HA-MA-AM)在溶液以及土壤环境中的性质。当腐植酸钾用量低于40wt%时,在环境pH值为6～7的条件下,HA-MA-AM的吸水倍率明显高于未添加腐植酸钾的MA-AM型保水剂。实验结果表明,HA-MA-AM具有较好保持水分、抑制水分蒸发的作用。     

微滤法脱除皮革废水中有机物性能的研究

研究了微滤法脱除皮革废水中有机物的性能,并考察了其影响因素,对其主要操作条件进行了优化.试验中以COD指标来表征微滤法对有机物的脱除性能.其对皮革废水中COD去除率约为40%,酸性条件有利于COD去除,最佳操作pH为5,且蛋白质并不是影响皮革废水中COD水平的主导因素.同时比较了微滤法、活性炭吸附、生物吸附、超滤等方法对皮革废水中COD的脱除性能.     

苯酚产需现状及市场分析

2000年世界苯酚总生产能力约为740万t/a,总消费量为636万t/a,主要用于生产双酚A和酚醛树脂。预计世界苯酚需求将以每年4％-5％的速度增长。美国、西欧和日本是世界上3个最主要的苯酚生产国家和地区,北美地区的总生产能力为300万t/a,占世界总产能的40.6％,而德国酚化学公司是世界最大的苯酚生产厂家,其产能为145万t/a,占世界总产能的19.6％。2000年,我国有30家苯酚生产企业,总生产能力为28.9万t/a,总产量为24.94万t/a,主要用于酚醛树脂和水杨酸的生产。在1996-2000年间,中国大陆苯酚的净进口量分别为9.79万t、6.22万t、3.72万t、7.38万t和9.69万t,从2000年9月开始,从中国台湾的苯酚进口量增长很快。为增强市场竞争力,中国大陆苯酚生产企业应提高单套装置的生产能力,采用一体化生产模式。     

Trans FA and solid fat contents of margarines marketed in Turkey

Trans FA (TFA), solid fat contents (SFC), and slip melting points of 12 different tub and stick margarines marketed in Turkey were examined in this study. No trans isomers were found in four margarines, which suggests they were formulated from interesterified or blended fats and oils. The products with no TFA generally had more short-chain saturated FA, which suggests coconut oil-based oil components. TFA content of the other 10 products varied from 7.7 to 37.8%. Compared to the products formulated in North America, Turkish margarines contain more TFA and have higher SFC.