有机盐酸尾气吸收设备的改造

有机盐酸尾气吸收设备的介质为有机盐酸、游离氯和微量强溶解性有机溶剂,对浸渍石墨和钢衬PE/PO设备都有溶解作用。在不改变工艺设计的情况下,将尾气吸收设备改型为填料式吸收塔,通过改造材料、液体分布器、填料支撑栅板和多孔板结构,有效解决了尾气吸收塔故障率高和使用寿命短的问题,对其在强酸、有机酸和其他恶劣工况下的应用有很好的借鉴、推广意义。

示波极谱滴定法测定有机碱盐酸盐类药物

用示波极谱滴定法测定有机碱盐酸盐类药物,快速、准确,易检测出最终结果,节省药品.所测结果与药典法无显著差异.

氯化铵及有机碱盐酸盐分解反应的影响因素

氯化铵是联合制碱中的一种副产品,为实现氮元素和氯元素的高效利用,从根本上解决联碱工业中副产品过剩与环境污染问题,选择几种不同结构的有机碱,对有机碱作用下的氯化铵分解释放氨气和有机碱盐酸盐分解释放氯化氢的反应过程进行了研究,关联了有机碱碱性、结构及溶剂化作用对分解反应的影响。研究结果表明,有机碱碱性对氯化铵分解以及相应有机碱盐酸盐的分解并没有呈现出完全的正相关性。除碱性的影响外,有机碱对分解反应的影响还与有机碱自身的结构及溶剂化作用有关。三己胺和三辛胺是能够同时实现氯化铵分解和相应有机碱盐酸盐分解的适宜有机碱。溶剂对分解反应影响很大,在三己胺和三辛胺作用下的氯化铵分解反应需要在极性的醇溶剂中进行,而相应有机碱盐酸盐的分解则需要以非极性的烷烃为溶剂。

有机胺盐酸盐/B(C_6F_5)_3催化的酸与炔烃选择性加成反应研究

一直以来寻找直接有效的乙烯基官能化合成方法的研究备受关注.报道了一种新型的有机胺盐酸盐/B(C_6F_5)_3(BCF)体系催化炔烃与氢氯酸或羧酸的加成反应方法,可选择性地在炔烃的C(2)位氯代或羧化.研究了在有机胺盐酸盐/BCF体系催化下,不同取代的炔烃与无机酸HCl的氢氯化加成反应.在2,2,4,4-四甲基哌啶盐酸盐/BCF([TMPH]+[Cl-B(C_6F_5)_3]-)催化下,等物质的量的炔烃和HCl反应时,端基芳炔的C(2)位一加成产物的比例可高达90%以上,而端基烷基炔烃的选择性较芳炔差,叔丁基乙炔的一加成产物只占到67%.报道了非金属催化剂路易斯酸BCF催化的炔烃与羧酸CF_3COOH的烯醇酯化反应,端基芳炔的C(2)位烯醇酯化产率可达95%以上,而二苯基乙炔及非芳香性端基炔的反应活性较低.首次实现了非金属催化剂FLPs参与催化的炔烃与酸的选择性氢氯化和烯醇酯化加成反应.

新型B(C_6F_5)_3/有机胺盐酸盐催化体系的反应研究

近年来,受限路易斯酸碱对(FLPs:Frustrated Lewis Pairs)在小分子的活化以及在催化还原等方面所表现出的独特反应特性,使得有关FLPs化学的研究受到了国内外广泛的关注.设计了一种新型的FLPs催化体系,该体系以三(五氟苯基)硼(BCF)为路易斯酸,以多种不同取代的有机胺盐酸盐替代常规FLPs中的路易斯碱有机胺.发现利用该体系与氢化硅烷反应,不仅可以高产率地制备分离得到相应的伯、仲、叔硼氢化胺盐;而且还可以这一体系作为催化剂,以氢化硅烷作为还原剂,在常温常压下可高选择性地部分或彻底还原大部分含羰基官能团醛酮等有机化合物.由BCF/2,2,6,6-四甲基哌啶(TMP)盐酸盐组成的催化体系在对CO2催化还原为甲烷的反应中,亦较相应的BCF/TMP体系显示更高的活性.还通过核磁共振详细地对比研究了原料有机胺盐酸盐、中间体氯代硼胺盐以及产物氢化硼胺盐中,胺基氮上质子的核磁共振谱信息,发现不仅胺基上取代基的位阻效应会影响到具有电四极矩性的14N磁性核的弛豫效应,而且阴离子基团的配位强弱对胺基氮上质子的化学位移也会产生较大的影响.

Phosphate-Solubilizing and -Mineralizing Abilities of Bacteria Isolated from Soils

Microorganisms capable of solubilizing and mineralizing phosphorus （P） pools in soils are considered vital in promoting P bioavallability. The study was conducted to screen and isolate inorganic P-solubilizing bacteria （IPSB） and organic P-mineralizing bacteria （OPMB） in soils taken from subtropical flooded and temperate non-flooded soils, and to compare inorganic P-solubilizing and organic P-solubilizing abilities between IPSB and OPMB. Ten OPMB strains were isolated and identified as Bacillus cereus and Bacillus megaterium, and five IPSB strains as B. megaterium, Burkholderia caryophyUi, Pseudomonas cichorii, and Pseudomonas syringae. P-solubilizing and -mineralizing abilities of the strains were measured using the methods taking cellular P into account. The IPSB strains exhibited inorganic P-solubilizing abilities ranging between 25.4-41.7 μg P mL^-1 and organic P-mineralizing abilities between 8.2-17.8μg P mL^-1. Each of the OPMB strains also exhibited both solubilizing and mineralizing abilities varying from 4.4 to 26.5 μg P mL^-1 and from 13.8 to 62.8 μg P mL^-1, respectively. For both IPSB and OPMB strains, most of the P mineralized from the organic P source was incorporated into the bacterial cells as cellular P. A significantly negative linear correlation （P 〈 0.05） was found between culture pH and P solubilized from inorganic P by OPMB strains. The results suggested that P solubilization and mineralization could coexist in the same bacterial strain.

Hierarchical cobalt phenylphosphonate nanothorn flowers for enhanced electrocatalytic water oxidation at neutral pH

Cobalt-based phosphate/phosphonates are a class of promising water oxidation catalysts at neutralpH.Herein,we reported a facile hydrothermal synthesis of various nanostructured cobalt phe-nylphosphonates.It is found that the number of hydroxyl group of structure-directing reagent iscrucial for the construction of 3D hierarchical structures including hierarchical nanosheet flow-er-like assemblies and nanothorn microsphere.These samples were characterized by scanningelectron microscopy,transmission electron microscopy,X-ray diffraction,infrared,and X-ray pho-toelectron spectroscopy techniques.They can act as highly efficient electrocatalysts for the oxygenevolution reaction at neutral pH.Among these,hierarchical cobalt phenylphosphonate nanothornflowers present excellent performance,affording a current density of 1 mA cm^-2 required a smalloverpotential of 393 mV.This work offers a new clue to develop high-performance metal phospho-nate/phosphate catalysts toward electrochemical water oxidation.

The Burial of Biogenic Silica, Organic Carbon and Organic Nitrogen in the Sediments of the East China Sea

We sampled the sediments of the East China Sea during 2005 and 2006, and analysed the contents of the biogenic matters: biogenic silica, organic carbon, and organic nitrogen. From the surface distribution we found the contents of these substances to be in the ranges of 0.72%-1.64%, 0.043%-0.82%, and 0.006%-0.11%, respectively. Their distributions were similar to each other, being high inside the Hangzhou Bay and low outside the bay. The vertical variations of the contents were also similar. In order to discuss the relation between them we analysed the variations of content with depth. They increased in the first 7 cm and then decreased with depth. The peaks were found at depths between 20 to 25 cm. The distribution of carbonate showed an opposite trend to that of biogenic matters. The content of total carbon was relatively stable with respect to depth, and the ratio of high organic carbon to carbonate showed a low burial efficiency of carbonate, which means that the main burial of carbon is organic carbon. In order to discuss the source of organic matters, the ratio of organic carbon to organic nitrogen was calculated, which was 8.01 to 9.65, indicating that the organic matter in the sediments was derived mainly from phytoplankton in the seawater.

P Fractions in Drainage Waters from the Broadbalk Continuous Wheat Experiment at Rothamsted

Total P (TP), total participate P (PP), total dissolved P (TDP), molybdatereactive P (MRP) and dissolved organic P (DOP) were determined in waters from pipe-drains (at 65-cmdepth) from the Broadbalk Experiment at Rothamsted Research, UK. Average TPand PP exceeded 1 mgL^(-1) in about half of the 12 plots receiving superphosphate for the 5 measurements taken betweenDecember 2000 and April 2001. Ranging between 33.8% and 87.3% of TP, PP was the largest P fractionin drainage waters, with DOP, ranging from 0.5% to 26.2% of TP, being the smallest fraction Meanproportions of PP, MRP and DOP in TP in drainage waters were 63.4%, 32.5% and 4.1%, respectively.These findings support previous findings that P losses from soil to drainage waters were muchlargerthan previously thought, and could therefore make a significant contribution to eutrophication.

Solvothermal synthesis of Co-substituted phosphomolybdate acid encapsulated in the UiO-66 framework for catalytic application in olefin epoxidation

Hybrid composites of phosphomolybdic acid@UiO-66(PMo12@UiO-66)and Co-substituted phosphomolybdic acid@UiO-66(PMo11Co@UiO-66)were synthesized using the direct solvothermal method.A variety of characterization results demonstrated that phosphomolybdic acid(PMo12)or Co-substituted phosphomolybdate acid(PMo11Co)clusters are uniformly dispersed in the cages of Zr-based metal-organic UiO-66 frameworks.The catalytic properties of these hybrid composites were investigated by applying the epoxidation of olefins with tert-butyl hydroperoxide as the oxidant.Compared to PMo12@UiO-66,PMo11Co@UiO-66 showed a much higher catalytic activity and was simply recovered by filtration and reused for at least ten runs without significant loss of catalytic activity.Particularly,PMo11Co@UiO-66 can efficiently convert cyclic olefins like limonenes to epoxides,and its selectivity to 1,2-limonene oxide reached 91%in the presence of a radical inhibitor such as hydroquinone.The excellent catalytic activity and stability of the hybrid composite PMo11Co@UiO-66 are mainly attributed to the uniform distribution of highly active PMo11Co units within the smaller cages of UiO-66,to the suitable surface polarity of the hybrid composite for facilitating the access of reagents and solvent,and to the strong interface-interactions between the polyoxometalate and the UiO-66 framework.

Synthesis of glycerine-xanthate and its depressing mechanism in separation of marmatite from arsenopyrite

A small molecular organic depressor glycerine-xanthate was synthesized. The effect of glycerine-xanthate on the flotation of sulfide minerals was investigated based on a function of pH value and concentration of glycerine-xanthate through flotation experiments in the presence and absence of Cu^2＋. The results show that glycerinee-xanthate has a strong dressing effect on marmatite at pH〉6 and on arsenopyrite in weak acid and base conditions with butyl-xanthate as collector. In the presence of glycerine -xanthate, marmatite is activated by addition of Cu^2＋, but arsenopyrite cannot be activated and remains unfloatable. So the selective separation can be achieved for two minerals. The depression of glycerine-xanthate on sulfide minerals was discussed based on the radical electronegative calculation and the theory of HSAB. Infrared spectrum shows that there are some -OH and-CSS-in glycedne-xanthate molecule, which competes with butyl-xanthate on the mineral surface. As a result of many hydrophilic groups in glycerine-xanthate, the surfaces of marmatite and arsenopyrite become hydrophilic, thus the flotation of marmatite and arsenopyrite is depressed. The collector is adsorbed preferentially on the surface of marmatite and it shows a better floatability in the presence of Cu^2＋, whereas, the surface of arsenopyrite absorbs glycerine-xanthate and the flotation of arsenopyrite is depressed by glycerine-xanthate.

Phosphate Rock Fertilizer in Acid Soils: Comparing Phosphate Extraction Methods for Measuring Dissolution

Three phosphate extraction methods were used to investigate the dissolution, availability and transformation of Kunyang phosphate rock (KPR) in two surface acid soils. Dissolution was determined by measuring the increase in the amounts of soluble and adsorbed inorganic phosphate fractions, and did not differ significantly among the three methods. Significant correlations were obtained among P fractions got by the three extraction methods. Dissolution continued until the end of the 90 day incubation period. At the end of the period, much of the applied phosphate recovered in both soils were in the Al and Fe P or in the hydroxide and bicarbonate extractable inorganic P fractions. The dissolution of KPR in the two soils was also similar: increased addition of phosphate rock resulted in decreased dissolution. The similarity in the order and extent of dissolution in the two soils was probably due to the similarity in each soil of several factors that are known to influence phosphate rock dissolution, namely low CEC, pH, P level, and base status; and high clay and free iron and aluminum oxide contents. The results suggested that KPR could be an alternative P source in the long, if not the short, term in the soils, provided that those factors influencing P availability in the soils are not limiting.

Studies of Cyclohexane Catalytic Oxidation Processes over Titanium Silicate-1 Zeolite

The catalytic oxidation processes for cyclohexane/H_2O_2/acetone system overthe TS-1 zeolite was studied. Study results have revealed that the cyclohexane conversion was 27%after the reaction proceeded at 100℃ for 2 hours at a cyclohexane/H_2O_2 molar ratio of 0.8. Thecyclohexanol/cyclohexanone molar ratio was 1.3 along with a certain amount of organic acids andesters, the formation of which was closely associated with the oxidation of reaction solvent anddeep oxidation of cyclohexanone and cyclohexanol contained in the reaction products. With respect tothe catalytic oxidation of cyclohexane/H_2O_2 system the selection of appropriate solvent wascritically important.

Indirect Radiative and Climatic Effects of Sulfate and Organic Carbon Aerosols over East Asia Investigated by RIEMS

The indirect radiative and climatic effects of sulfate and organic carbon aerosols over East Asia were investigated using a Regional Integrated Environment Model System (RIEMS) with an empirical aerosol-cloud parameterization.The first indirect radiative forcing was negative and ranged from-9-0 W m-2 in the domain.The maximum cooling,up to-9 W m-2,occurred in the Chongqing District in winter,whereas the cooling areas were larger during summer than in winter.Organic carbon (OC) aerosols were more abundant in winter than in summer,whereas the sulfate concentration during summer was much higher than during winter.The concentrations of sulfate and OC were comparable in winter,and sulfate played a dominant role in determining indirect radiative forcing in summer,whereas in winter,both sulfate and OC were important.The regional mean indirect radiative forcings were-0.73 W m-2 and-0.41 W m-2 in summer and winter,respectively.The surface cooling caused by indirect effects was more obvious in winter than that in summer.The ground temperature decreased by ～1.2 K in most areas of eastern China in winter,whereas in summer,the temperature decreased (～-1.5 K) in some regions,such as the Yangtze River region,but increased (～0.9 K) in the areas between the Yellow and Yangtze Rivers.In winter,the precipitation decreased by 0-6 mm in most areas of eastern China,but in summer,alternating bands of increasing (up to 80 mm) and decreasing (～-80 mm) precipitation appeared in eastern China.

Peroxymonosulfate activation by Mn_3O_4/metal-organic framework for degradation of refractory aqueous organic pollutant rhodamine B

An environmentally friendly Mn‐oxide‐supported metal‐organic framework(MOF),Mn3O4/ZIF‐8,was successfully prepared using a facile solvothermal method,with a formation mechanism proposed.The composite was characterized using X‐ray diffraction,scanning electron microscopy,transmission electron microscopy,X‐ray photoelectron microscopy,and Fourier‐transform infrared spectroscopy.After characterization,the MOF was used to activate peroxymonosulfate(PMS)for degradation of the refractory pollutant rhodamine B(RhB)in water.The composite prepared at a0.5:1mass ratio of Mn3O4to ZIF‐8possessed the highest catalytic activity with negligible Mn leaching.The maximum RhB degradation of approximately98%was achieved at0.4g/L0.5‐Mn/ZIF‐120,0.3g/L PMS,and10mg/L initial RhB concentration at a reaction temperature of23°C.The RhB degradation followed first‐order kinetics and was accelerated with increased0.5‐Mn/ZIF‐120and PMS dosages,decreased initial RhB concentration,and increased reaction temperature.Moreover,quenching tests indicated that?OH was the predominant radical involved in the RhB degradation;the?OH mainly originated from SO4??and,hence,PMS.Mn3O4/ZIF‐8also displayed good reusability for RhB degradation in the presence of PMS over five runs,with a RhB degradation efficiency of more than96%and Mn leaching of less than5%for each run.Based on these findings,a RhB degradation mechanism was proposed.

Microbial Solubilization of Phosphorus from Nano Rock Phosphate

Phosphorus （P） is a major growth-limiting nutrient, and unlike the case of nitrogen （N）, there is no large atmospheric source that can be made biologically available. Moreover, P governs crucial role in plant as it stimulates root development and growth, gives plant rapid and vigorous start leading to better tillering and essential for many metabolic processes for seed formation. Soil microbes play very important role in bio-weathering and biodegradation. The microorganisms produce low molecular mass organic acids, which attack the phosphate structure and transform phosphorus from non-utilizable to the utilizable for the plants form. The test of the relative efficiency of isolated strains is carried out by selecting the microorganisms that are capable of producing a halo/clear zone on a plate owing to the production of organic acids into the surrounding medium. It is a well-known fact that as the particle size of rock phosphate decreases, the microbe mediated solubilization of rock phosphate increases in soil. In the present investigation, microbial solubilization of nano rock phosphate （〈 100 nm） particles was studied. Experimental results revealed that Pseudomonas striata solubilized 11.45% of the total P after 24 h of incubation from nano rock phosphate particles while 28.95% and 21.19% of the total P was solubilized by Aspergillus niger （black pigmented） and Aspergillus niger （green pigmented）, respectively. It was also observed that Aspergillus niger has the higher ability to dissolve Udaipur rock phosphate than Pseudomonas striata.

A comparative effect of 3 disinfectants on heterotrophic bacteria, iron bacteria and sulfate-reducing bacteria

The disinfection effect of chlorine dioxide, chlorine and their mixture on heterotrophic bacteria, iron bacteria and sulfate-reducing bacteria in circulating cooling water was studied. The results of the test indicated that high purity chlorine dioxide was the most effective biocide in the 3 disinfectants, and with a dosage of 0.5 mg/L, chlorine dioxide could obtain perfect effect. High purity chloride dioxide could have the excellent effect with the pH value of 6 to 10, and could keep it within 72 h. Chlorine and their mixture couldn’t reach the effect of chlorine dioxide.

Toxic Effects of Phthalates on Ocean Algae

This article discusses the interaction of phthalates and ocean algae based on the standard appraisal method of chemical medicine for algae toxicity. Through the experiments on the toxic effects of dimethyl (o-) phthalate (DMP), diethyl (o-) phthalate (DEP), dibutyl (o-) phthalate (DBP) on ocean algae, the 50 % lethal concentration of the three substances in 48 h and 96 h for plaeodectylum tricornutum, platymonas sp, isochrysis galbana, and skeletonema costatum is obtained. Tolerance limits of the above ocean algae of DMP, DEP, and DBP are discussed.

Recovery of Gold from Aqueous Solution Containing Au（Ⅲ） by Silicon Organic Polymer

The silicon organic polymer containing PSOT-3 （dioxothiocarbamide groups） has been synthesized and characterized, and the adsorption of Au（III） on PSOT-3 was investigated. The results showed that PSOT-3 had good adsorption capacity for Au（III）, and the adsorption of Au（III） was found to be the most effective in 0.1-0.3 mol/dm^3 hydrochloric acid solution. The adsorption is physical and the process is endothermic, and Freundlich isotherm fits the data better than the Langmuir isotherm. The adsorption can be generally described by electrostatic interaction （Coulomb＇s force） between the adsorbent and the adsorbate. The high adsorption capacity of this sorbent has significant potential for gold recovery from aqueous solutions.

Pedogenic Carbonate and Soil Dehydrogenase Activity in Response to Soil Organic Matter in Artemisia ordosica Community

Little attention has been paid to the role of soil organic matter （OM） in the formation of pedogenic carbonate in desert soils. The relationships among soil OM, soil dehydrogenase activity （DHA）, and soil CaCO3 in a plant community dominated by Artemisia ordosica, located on the eastern boundary of Tcngger Desert in the Alxa League, Inner Mongolia, China, were studied to understand whether OM was directly involved in the formation of pedogenic carbonate. The results showed that DHA and CuCO3 positively correlated with OM content, and DHA, OM, and CaCO3 were correlated with each other in their spatial distribution, indicating that abundant OM content contributed to the formation of CaCO3. Therefore, the formation of pedogenic CaCO3 was a biotic process in the plant community dominated by A. ordosica.