Vital-Fluorochromization of Microorganisms Using 3′,6′-Diacetylfluorescein to Determine Damages of Cell Membranes and Loss of Metabolic Activity by Ozonation

Cell suspensions of Escherichia coli as a model for bacterial populations in wastewaters were treated with ozone as a disinfectant in a continuously operated pilot plant with a plug flow reactor. Suspensions with an initial number of CFU (colony forming units) of 10⁸ mL^?1 were ozonized with ozone concentrations up to 12 mg/L. Metabolic activities and membrane functions break down with increasing ozone concentrations. The fluorochromization using 3′,6′-diacetylfluorescein (FDA) proved to be a suitable method for the detection of an alteration in permeability of the cell membranes and an inactivation of metabolic activity. By fluorescence microscopic and photometric investigations it could be clearly demonstrated that, in the case of disinfection with ozone, inactivation of the cells includes first of all a damage of the cell membranes. In contrast to the determination of the number of CFU, fluorochromization allows the detection of alteration in metabolic activities.     

亲电聚合路线合成聚醚醚酮酮砜的研究

用4,4′-二苯氧基二苯砜(DPODPS)分别与对苯二甲酰氯(TPC)、间苯二甲酰氯(IPC)或2,5-二氯对苯二甲酰氯(DCC)在1,2-二氯乙烷(DCE)中,以无水 AlCl_3为催化剂,在 N-甲基吡咯烷酮(NMP)存在下,通过付-克亲电聚合反应,制得了五种不同结构的聚醚醚酮酮砜(简称PEEKKS)。用红外光谱(IR)、X-射线衍射(XRD)、扫描电镜(SEM)、差示扫描量热(DSC)、热重(TG)及耐溶剂试验,对聚合物进行了表征。结果表明,五种聚合物的对数比浓粘度(η_(inh))均达到0.85以上.具有较低的熔融温度、良好的溶解性能和耐高温性能,PEEKKS 属于非晶态聚合物。     

Photostability of polyetherurethaneureas

Polyetherurethaneureas (PEUUs) were synthesised from polyethylene-glycols (PEGs) of molecular weight 400, 600 and 1000, 4,4′-diphenylmethanediisocyanate (MDI) and aliphatic diamine chain extenders, 1,3-propanediamine (PDA) and 1,6-hexanediamine (HDA). Polymer films were irradiated with 365 nm light at 293 K and the effects of polyether soft segment length and urea hard segment on photo-oxidative stability were studied by following the variation in weight-average molecular weight (M _w), gel formation and stress-strain properties. Changes in ultraviolet and infrared spectroscopy were monitored on photo-oxidation and hydroperoxide content determined. The soft segment length was increased by increasing the molecular weight of PEG from 400 to 1000 and hard segment structure was changed by variation of diamine. It was noted that the structure of urea and polyether soft segment length plays an important role in photostability of PEUUs. PDA chain extended PEUUs were more stable than HDA chain extended PEUUs.     

Optical data storage by novel photoelectrochromic polymer

A novel elastic polymer containing 4,4′-bipyridinium salts with tetrakis[3,5-bis(trifluoromethyl)phenyl]borate as part of the main chain was synthesized. The cast film showed persistent and reversible colour changes due to photoinduced electron transfer upon excitation of an ion-pair charge-transfer band (_ex >365 nm) in vacuo. The lifetime of the coloured state markedly depended on temperature. The optically written data were stored without decay below 0°C and were erased thermally at elevated temperatures. The colour changes were reversibly repeatable for many times.     

Synthesis and characterization of novel diimide–dinaphthols and resulting poly(urethane–imide)s

Novel diols containing imide groups were prepared via condensation of aromatic dianhydrides with 5‐amino‐1‐naphthol. The diimide–dinaphthols prepared were characterized by conventional methods and used to synthesize new poly(urethane–imide)s (PUIs). All the polymers were characterized and their physical properties, such as solubility, solution viscosity, thermal stability, and thermal behaviour were studied. The polymers obtained showed more thermal stability than typical polyurethanes because of the presence of the imide groups. Copyright © 2003 Society of Chemical Industry     

Preparation of High Strength and Toughness Aramid Fiber by Introducing Flexible Asymmetric Monomer to Construct Misplaced-Nunchaku Structure

High performance fibers with high strength and toughness have great potential in composites, but contradiction between tensile strength and elongation at break makes the preparation to become a current challenge. Herein, an asymmetric structure of more flexible diamine, 3,4′-diaminodiphenyl ether (3,4′-ODA), is introduced into heterocyclic aramid (PBIA) fibers to replace rigid symmetric p-phenylenediamine (PDA). By studying the properties of copolymer (mPEBA) fibers with different ratios of diamine, it is found that the mPEBA fiber reached the optimal mechanical properties with the 30% content of 3,4′-ODA. Compared with homopolymerized heterocyclic aramid fibers, the tensile strength and elongation at break of mPEBA fiber are improved by 26.2% and 38.7%, respectively. Results of X-ray diffraction show that the introduction of 3,4′-ODA structure can increase stretchability of mPEBA fibers, improving the orientation degree during hot-drawing. Molecular dynamics simulations confirm that 3,4′-ODA structure undergoes a conformation transformation to form a straightened chain during hot-drawing, while symmetrical 4,4′-diaminodiphenyl ether (4,4′-ODA) cannot form the same conformation. The misplaced-nunchaku structure is formed based on the special meta-para position of 3,4′-ODA, achieving the synergy of high strength and high toughness.     

四异丁氧基镍酞菁的合成及其溶剂效应

4 异丁氧基邻苯二腈与氯化镍在强有机碱 1 ,8 二氮杂双环 (5 ,4,0 )十一碳烯 7催化下反应 ,合成了四异丁氧基镍酞菁 ,产物经FT -IR、元素分析、UV -Vis吸收光谱和1 H NMR表征了结构 ;并研究了其溶剂效应 ,结果表明 :最大吸收峰波数ν与函数 f(n ,ε)存在一定的线性关系 ,线性相关系数为 0 940 2 ,而Bayliss函数项 (n2 - 1 ) /(2n2 +1 )决定了最大吸收波长 (λmax)的位移变化 ;化合物的λmax在不同溶剂中随聚集程度增加 ,发生一定程度的蓝移     

3-氯-4-（2-溴甲基-4-甲基-1，3-二恶戍烷-2-基）苯基-4’-氯苯基醚的合成

3-氯-4-（2-溴甲基-4-甲基-1，3-二恶戍烷-2-基）苯基-4’-氯苯基醚是杀菌剂苯醚甲环唑的一个重要中间体。以2-氯-4-（4-氯苯氧基）-苯乙酮为起始原料，采用溴化和合环同时进行的合成工艺制得该化合物，收率90％．产品含量95％。优化了反应条件，简化了操作。     

N,N′-乙撑双[N(乙磺酸钠)-十二酰胺]的合成与性能评价

以乙二胺、2-氯乙基磺酸钠、月桂酸等为原料合成了N,N′-乙撑双[N(乙磺酸钠)-十二酰胺](简记为DTM-12)。以IR和1HNMR对其结构进行了初步表征。该目标产物水溶液的CMC(0.5 mmol/L)分别是十二烷基硫酸钠和十二烷基磺酸钠的1/16和1/20,γCMC(29.7 mN/m)低8~9 mN/m。DTM-12分别与十二烷基三甲基溴化铵(DTAB)和辛基酚聚乙氧基醚9-10EO(Triton X-100)组成的复配体系在摩尔比为3∶7时,CMC达到0.106和0.049 mmol/L,γCMC达到25.4和31.7 mN/m,优于十二烷基磺酸钠组成的复配体系。DTM-12还具有良好的起泡性和稳泡性。     

双酚单丙烯酸酯类抗氧剂GM的合成

以2,2′-甲撑双(4-甲基-6-特丁基苯酚)(简称2246)、丙烯酸、氯氧化磷等为反应原料,通过酯化反应合成了GM,考察了合成GM的适宜工艺条件。在n(2246)∶n(丙烯酸)∶n(氯氧化磷)=1∶1.25∶0.90、催化剂m(三乙胺)∶m(2246)=1∶1.0X、反应温度105℃、反应时间2.5 h的合成条件下,原料2246转化率大于96.0%;GM产品选择性大于91.0%;GM产品摩尔收率大于83.0%;GM产品的液相色谱纯度大于99.0%。采用该工艺合成抗氧剂GM的特点是将酰卤化过程和脱卤化氢过程合二为一,由2246和丙烯酸直接进行酯化反应合成GM。工艺流程短,产品收率高、质量稳定,有可能便于工业化生产。