一种新型高效水解酸化与低氧生化的组合工艺研究

本文通过对某炼油及乙烯一体化项目中的丙烯腈及丙烯腈-丁二烯-苯乙烯共聚物(ABS)混合污水的预处理工程实例介绍,重点阐述了一种新型高效水解酸化加低氧生化组合工艺的原理和特点,分析其在丙烯腈及ABS混合废水预处理中的适用性和优势,并介绍了该工艺的主要参数与运行情况。

新型分流转向酸化工艺在塔里木油田DH1-H2井的应用

塔里木东河油田砂岩水平井埋藏深度大(平均达5800 m),温度高(达140℃),水平井段长,以筛管完井为主,这些特征制约了多种改造工艺的应用,只能进行笼统酸化。结合目前分流转向酸化工艺技术的发展方向,创新研制了DCF温度降解型颗粒转向剂和用于高温砂岩储层的清洁转向酸体系。DCF颗粒转向剂随主体酸持续或间断注入实现分流转向,达到均匀布酸的效果;砂岩清洁转向酸不含聚合物,其与碳酸盐反应增粘实现长水平井段的高效布酸,并消耗近井碳酸盐成分,更加利于清洁改造。新型分流转向酸化工艺在DH1-H2井的探索性应用取得显著效果。

气浮-水解酸化-高效接触氧化工艺处理汽车废水

对某汽车公司的废水处理系统进行了改造,采用气浮-水解酸化-高效接触氧化工艺对其废水进行了处理,在水解酸化池中使用生物微电解填料,在接触氧化池内使用LK40弹性立体网状生物亲和性组合填料。经该体系处理后,出水水质为pH=6～9、SS<60mg/L、CODCr<90mg/L、BOD5<20mg/L、石油类<5mg/L,达到DB44/26-2001中一级标准,其处理费用为1.91元/m3。

高效水解酸化废水处理技术功效与机理思考

随着我国经济水平的不断提升,各项能源与资源的使用也逐步增加,而在所有资源中,水资源的供应与需求矛盾也日益突出。与此同时,城市每天都会产生大量的废水,在此背景下,我国的水污染不断加剧。用高效水解废水处理技术处理废水,可在一定程度上减少废水的产生,让其达到可以向外排放的标准。

Preliminary Studies on High-performance Liquid Chro-matography Chemiluminescence Determination of theSaturated Fatty Acids(C_(16) C_(18))in Human Serum

The peroxyoxalate chemiluminescence(CL)detection of fatty acids in human se- rum combined with high-performance liquid chromatography (HPLC)is described.Some fatty acids in serum were extracted with a 1 :1(v/v)mixture of chloroform-n-heptane.2-(4-Hydrazinocarbonyl- phenyl)-4,5-diphenylimidazole (HCPI) was used as a fluorescent labelling reagent of the fatty acids. The labelling reaction was carried out at 30℃ for 1 h at pH 6.5 and the resulting reaction mixture was sudjected to HPLC. The labelled fatty acid C_(17)(P-C_(17))was used as the internal standard. The la- belled fatty acids C_(16) and C_(18) were separated within 18 min on an ODS-8OTM column (150 mm× 6 mm ID,5μm,Tosoh Japan).The calibrlation curves of fatty acids from the spiked control serum were Y_1=-0.003 7 + 0.0028X_1,r=0.994 for FA C_( 16) and Y_2=0.00 1 2 + 0.00098X_2,r=0.999 for FA C_( 18),respectively.The average recoveries of facids from the spiked contrl serum were 107.2%(n=8,RSD=4.3%)for FA C_(16) and 97.35%(n=8, RSD=4.0%)for FA C_(18),respectively.The lower detection limits of fatty acids after reaction were 12μmol per 20μl injection for FA C_(16) and 18 μmol per 20μl injection for FA C_(18),respectively(signal to noise ratio, S/N=2).The HPLC/CL method was applied to the determination of FA C_(16) and FA C_(18) in normal human serum and the results showed that the concentrations of fatty acids in normal human serum were 0.134 ± 0.009 μ mol/ml serum(n=5) for FA C_(16) and 0.052±0.028 μmol/ml serum(n=5)for FA C_(18),respectively.

Solid Acid Used as Highly Efficient Catalyst for Esterification of Free Fatty Acids with Alcohols

Anovel solid acid catalyst, which was prepared from sodium alginate (SA) and metal chlorides and characterized with XRD and FT-IR spectrometry, was used for the preparation of biodiesel via esterification reaction. The study results showed that the aluminum-alginate complex prepared in a cheap and easy way exhibited high catalytic activity, and a 92.6% conversion of methyl oleate was obtained in the presence of 4m% of catalyst dosage upon refluxing for 3h of methanol and acid mixed in a molar ratio of 10:1. It should be noted that the catalyst can be applied to the esterification reaction of fatty acids with various carbon chain length on methanol or different short chain alcohols, indicating that the catalyst is suitable for the preparation of biodiesel from waste oils with a high acid value.

Determination of Baicalin in Traditional Chinese Preparation by High Performance Liquid Chromatography with Chemiluminescence Detection

A new method for the determination of baicalin with HPLC-CL was developed. The method was based on the chemiluminescence reaction between KMnO4 and baicalin sensitized from HCHO. The linear range was 3.7?0-6~9.8?0-5 mol/L with detection limit of 1.7?0-6 mol/L and the relative standard deviation was 2.5 % (Cs=6.6?0-5 mol/L, n=5). The method has been applied to the determination of baicalin in oral administration, injection, Scutellariae radix and granules with good results.

Functional Polyethylene Glycol with Carboxyl-supported Platinum as an Efficient Catalysis System for the Hydrosilylation of Alkenes

A series of carboxylated long chain polyethylene glycols(abbreviated as PEGCOOH) has been synthesized and used to support chloroplatinic acid.These supported catalysts were then tested for their efficiency in the hydrosilylation of alkenes.The factors affecting their catalytic properties,e.g.relative molecular mass of polyethylene glycol,reaction temperature,platinum content,and type of alkenes,have been studied.It was found that the activity of the platinum catalyst decreased with increasing length of the polyethylene glycol chain,and increased with reaction temperature.Moreover,these catalysts could be reused several times without a noticeable decrease in activity or selectivity.The reaction pathway leading to excellent selectivity for the β-adduct of hydrosilylation of alkenes with triethoxysilane catalyzed by this catalysis system was discussed.

Efficient Separation of Butyric Acid by an Aqueous Two-phase System with Calcium Chloride

One of the bottlenecks for bioproduction of butyric acid as bulk chemical is the difficulty in separating butyric acid from the fermentation broth,compared with the petroleum-based chemical synthesis method.In the present work,a novel separation methodology was developed based on an aqueous two-phase system with inor-ganic salts.Calcium chloride was screened out for effective separation of butyric acid from butyric acid-water-salt systems.Within appropriate concentration range of butyric acid and salt,butyric acid was enriched in the upper phase and most of calcium ions remained in the lower phase.This"salting out"effect is very efficient to separate butyric acid from the simulated butyrate fermentation broth,which consists of butyric acid and acetic acid with concentration ratio of 4︰1,so that the final ratio of butyric acid/acetic acid in the upper phase is improved to 9.87. The aqueous two-phase system was used to separate butyric acid from the actual fermentation broth with satisfac-tory result.

Microanalysis and preliminary pharmacokinetic studies of a sulfated polysaccharide from Laminariajaponica

A rapid, sensitive and reproducible high performance liquid chromatography （HPLC） method with post-column fluorescence derivatization has been developed to determine the amount of low-molecular- weight sulfated polysaccharide （GFS） in vivo. The metabolism of GFS has been shown to fit a two component model following its administration by intravenous injection, and its pharmacokinetic parameters were determined to be as follows： half-time of distribution phase （t1/2α）=11.2±2.93 min, half-time of elimination phase （tl/2α）=98.20±25.78 min, maximum concentration （Cmax）=110.53 gg/mL and peak time （Tmax）=5 min. The pharmacokinetic behavior of GFS was also investigated following intragastric administration. However, the concentration of GFS found in serum was too low for detection, and GFS could only be detected for up to 2 h after intragastric administration （200 mg/kg body weight）. Thus, the bioavailability of GFS was low following intragastric administration because of the metabolism of GFS. In conclusion, HPLC with post-column derivatization could be used for quantitative microanalysis and pharmacokinetic studies to determine the presence of polysaccharides in the serum following intravenous injection.

Effect of Curing Temperature on Mortar Based on Sustainable Concrete Material＇s and Poly-Carboxylate Superplasticizer

Nowadays, technologies in construction field have offered several kinds of chemical admixtures, which offer different behaviors at the fresh state of the batch and by consequence, it is resulted with different mechanical behaviors at the solid state of the mix. This study focused on the behavior of a new kind of admixture at fresh and solid states. Currently, the concrete material has become a very expensive material because the high price mostly of aggregates, representing the three quarters of the concrete components. By consequence, it costs money and on the other hand, it produces a lot of wastes. The main aspect which guides this study is to make a kind of concrete based mainly on local material and sustainable concrete material （SCM or waste material）, which is one very abundant material in quality and quantity, under the current tendency the results obtained in this study summarize up the importance of the temperature during the development of the mechanical characteristics of mortar, mainly on compressive strength at age of 28 days. This is in the case of the addition of limestone crushed additive by percentage of substitution.

Recent trends in the use of polyoxometalate-based material for efficient water oxidation

Polyoxometalates （POMs）, with their attractive topological and electronic properties, have been demonstrated over the last few decades to be efficient catalysts for many reactions. In a new direction, POMs having a purely inorganic framework are now being explored as efficient catalysts for water oxidation. This review focuses on very recent developments of POM-based catalysts for water oxidation to O2. In the very extensive family of POMs, tetra-core sandwich-type Ru- and Co-containing POM complexes, namely [Ru404（OH）2（H20）4（y-SiW10O36）2]10- and [CO4（H2O）2（a-PWgO34）2]10- exhibit the ability to facilitate water oxidation under electrocatalytic and/or photocatalytic conditions. However, it is concluded that much work still needs to be done to explain the catalytic mechanisms and optimize these catalytic systems. In addition, recent trends in using ionic liquids as media to modify the electrolytic environment and enhance water oxidation are highlighted.

A rapid and simple ultraperformance liquid chromatography coupled to tandem mass spectrometry(UPLC-MS/MS) method for the detection of glucuronic acid-conjugated steroid metabolites

In the present study, we effectively detected 10 steroids and glucuronic acid-conjugated steroid metabolites in 12 min by ultraperformance liquid chromatography coupled to tandem mass spectrometry （UPLC-MS/MS）. Steroids testosterone （T）, 5ct-dihydrotestosterone （DHT）, androsterone （ADT）, etiocholanolone （ETIO）, estradiol （E2） and their glucuronide conjugates were well-separated on an Eclipse Plus C18 column （2.1 mm×50 ram, RRHD 1.8μm）. The mobile phase consisted of a mixture of methanol and ultrapure water （containing I mM ammonium formate） at a ratio of 60：40 （v/v）, and the flow rate was set at 0.25 mL/min. The LC eluate was detected by electrospray ionization （ESI） source in both positive and negative ion modes. Neutral loss （NL of 176, 194, 211 and 229 Da in positive mode） and precursor ion （PI ofm/z 141,159 and 177 in positive mode and 75, 85 and 133 in negative mode） methods were applied for the detection of steroid glucuronides. The multiple reaction monitoring （MRM） transitions were m/z 289.3→97.1,291.3→105, 291.3→199.2, 273.2→145.4 and 255.2→159.1 for T, DHT, ADT, ETIO and E2 in positive mode, respectively; as well as m/z 463.3→85 for T glucuronide （T-G）, m/z 465.3→75 for DHT glucuronide （DHT-G）, ADT glucuronide （ADT-G）, ETIO glucuronide （ETIO-G） and m/z 447.3→271 for E2 glucuronide （Ez-G） in negative mode. In addition, the analytical method was also applied for the detection of steroid glucuronides in pooled human liver microsomes （HLM）, which might serve as a basis for further investigation of steroid metabolism in vivo and in vitro.

Efficient degradation of methyl orange via multilayer films of titanium dioxide and silicotungstic acid

We report layer-by-layer （LbL） assembly of TiO2 and H4SiW12O40 （SiW12） multilayer film on silicon wafers and glass slides for photocatalytic degradation of methyl orange （MO）. The photocatalytic efficiency of the obtained multilayer film increases along with the decrease of pH and salt concentration of the incubation solution. The results show that MO can be almost re- moved in pH 2.0 solution without salt addition in the first 60 min incubation when MO concentration is lower than 15 mg/L. Different salts show an apparent inhibitory effect on photocatalytic degradation of MO with the order of ZnC12〉KCI〉 NaC1〉LiCI. The TiO2/SiW12 multilayer film maintains photocatalytic activity even after five degradation cycles. The reaction of MO photodegradation accords with an apparent first-order dynamics.

A novel catalytic application of heteropolyacids:chemical transformation of major ginsenosides into rare ginsenosides exemplified by Rg1

High performance liquid chromatography coupled with quadruple-time-of-flight mass spectrometry(HPLC-Q-TOF-MS)method was developed for analyzing the hydrolytic mixtures of ginsenoside R_(g1) in acidic conditions(pH 3). Three catalysts, a heteropolyacid(H_4SiW_(12)O_(40), SiW_(12) for short), its complex with γ-CD(SiW_(12)/γ-CD for short) and formic acid, were used for comparison. The chemical transformation products were identified based on the accurate mass measurement and the fragment ions obtained from tandem mass spectrometry. It was concluded that the catalytic efficiency of SiW_(12)(≈SiW_(12)/γ-CD) is ca. 410 times higher than that of formic acid, thus becoming the most efficient catalyst for chemical transformations of ginsenosides.

Highly dispersed Pt species anchored on W_(18)O_(49)nanowires mediate efficient and durable hydrogen evolution in acidic water

Platinum-based material is the most efficient and durable electrocatalyst for motivating the hydrogen evolution reaction(HER)in an acidic electrolyte;however,its low abundance and high cost limit its further application in proton-exchange membrane water electrolysis(PEMWE)technology.Therefore,minimizing the Pt amount while retaining high activity would be desirable.Herein,we use defect-rich W_(18)O_(49)nanowires to anchor well-dispersed,ultrafine Pt species(Pt-W_(18)O_(49))via a freeze-drying method to avoid aggregation,further mediating an efficient and durable HER in acidic water.Density functional theory analyses also demonstrate that the strong electronic interaction between the Pt species and W_(18)O_(49)support greatly improves the HER performance.With a 1/10 Pt loading amount of the commercial 20 wt%Pt/C,the Pt-W_(18)O_(49)catalyst requires the overpotentials of 116 and 743 mV to achieve high current densities of 100 and 1000 mA cm^(−2)in 0.5 mol L^(−1)H_(2)SO_(4),outperforming those of the 20 wt%Pt/C benchmark.More importantly,the Pt-W_(18)O_(49)catalyst can sustain a high-currentdensity HER at 500 mA cm^(−2)for more than 38 h without obvious degradation.This work paves a new avenue for synergistically reducing the Pt amount and retaining high activity for real-world PEMWE.