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双语推荐:硝化纤维

选取机体Cu(Ⅱ)浓度,运用衰减全反射傅立叶变换红外光谱(ATR-FTIR)、SDS-PAGE电泳和冯克劳斯法,分析了Cu(Ⅱ)对过氧亚硝酸根介导的硝化反应中纤维蛋白原二级结构和凝聚活性的影响。结果显示:随着 Cu(Ⅱ)浓度的增加,硝化纤维蛋白原中110 kDa新增条带越来越清晰;二级结构中α-螺旋比例下降,β-折叠比例上升;凝聚活性逐渐降低;当Cu(Ⅱ)浓度为1.66 mmol·L-1时,硝化纤维蛋白原中的α-螺旋比例由最初的32.29%减少到25.15%,β-折叠比例从35.66%升高到44.47%;冯克劳斯法检测硝化纤维蛋白原失去凝聚能力,但 SDS-PAGE电泳表明其依然可以释放纤维蛋白单体。表明,Cu(Ⅱ)能显著影响硝化反应中纤维蛋白原的二级结构,抑制其凝聚活性,促进硝化损伤。
The concentration of Cu(Ⅱ)was selected in biomimetic system to analyze the influence of Cu(Ⅱ) on secondary structure changes and aggregation activity of fibrinogen in nitration reaction by peroxynitrite with the aid of ATR-FTIR,SDS-PAGE and Von Clauss method.The results showed that with the increase of Cu(Ⅱ) concentration,a 110 kDa band became more and more clearer,theα-helix proportion declined whileβ-fold pro-portion increased in the secondary structure of nitration fibrinogen,and aggregation activity decreased gradual-ly.When Cu(Ⅱ)concentration increased to 1.66 mmol·L-1,theα-helix proportion decreased from initial 32.29% to 25.15%,whileβ-fold proportion increased from 35.66% to 44.47%.The nitration fibrinogen lost aggregation activity as detected by Von Clauss method,though SDS-PAGE showed that it still could release fi-brin monomer.The research demonstrated that Cu(Ⅱ)could significantly influence the fibrinogen secondary structure changes during nitration react

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利用磷酸、硅烷偶联剂、硝化/还原改性剂等对芳纶纤维进行改性,再以改性后的芳纶纤维配抄芳纶纸,探讨芳纶纤维表面改性及其对芳纶纸物理性能的影响。结果表明,上述3种改性方法均可以改善芳纶纤维与芳纶浆粕界面的结合,从而提高芳纶纸的强度。
Phosphoric acid with different concentration ,silane coupling agent ,and nitration reduction were used in modifying of aramid fiber .The aramid fiber treated with different ways was mixed with aramid pulp to manufacture aramid paper sheets .Modification of ar-amid fiber and its effect on aramid paper properties were studied .Results show that above mentioned ways could significantly improve the interface of aramid fiber and pulp ,thus opti-mize the mechanical properties of aramid paper .

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以加拿大针叶木为原料、采用硝硫混酸和HNO3/CH2Cl2两种硝化剂分别制备了A、B、C、D级硝化纤维素(NC)样品,通过偏光显微镜分析测试了其含氮量及氮量分布(硝化均匀性)。同时采用不同的高压闪爆预处理条件,对针叶木进行预处理,比较了闪爆对高氮量B、低氮量D级NC的含氮量及氮量分布,系统研究了硝化剂体系组成及原料预处理条件对NC的含氮量及其分布影响规律。结果表明,在同样氮量级别,HNO3/CH2Cl2硝化体系比HNO3/H2SO4/H2O得到的NC氮量分布更均匀,A、B、C与D级NC的均匀性分别提高17.46%、16.98%、16.77%和25.79%;同一硝化剂体系,闪爆有利于硝化剂向软木纤维纤维束内部扩散,能提高NC含氮量及氮量分布均匀性,B级NC,其均匀性提高6.06%,D级NC则提高7.56%。
Nitrocellulose samples(NC)with A,B,C,and D grade were synthesized by nitrating Canadian softwood in HNO3/H2 SO4/H2 O and HNO3/CH2 Cl2 ,respectively. The nitrogen content and nitrogen content distribution( uniformity of nitration)of nitrocellulose were analyzed by a polarizing microscope. Using high-pressure steam explosion technology,soft wood was treated before processing. The effect of steam explosion treatment on the nitrogen content distribution of high nitrogen B and low nitrogen D grade NC was discussed. Results show that the nitrogen content distribution of nitration product from HNO3/CH2Cl2 is more u-niform than that of product from HNO3/H2 SO4/H2 O under the same nitrogen content condition. Uniformities of nitration indica-tors of NC of A,B,C and D grade improve by 16. 9%、17. 5%、16. 8% and 25. 7%,respectively. Steam explosion preprocess can improve nitrogen content and uniformity of product in the same nitrification system because the efficiency of nitration agents
随着硝酸盐氮的污染问题日益严重,人们对水质的要求也逐渐提高,寻求高效且经济的方法来去除水中的硝酸盐氮成为了一个重要的课题。本研究以此出发,研究了建立在电极生物膜反应器中的氢自养反硝化去除水中硝酸盐的方法。本实验采用碳棒作为阳极,活性炭纤维毡为微生物载体,水被电解后在阴极表面产生氢气,供固定在阴极表面的反硝化细菌直接利用进行氢自养反硝化作用。无需外加有机碳源,即可去除水中的硝酸盐氮,具有处理费用低、无二次污染、剩余污泥少等特点。
When the problem of drinking water poluted by the nitrate nitrogen is becoming more and more serious, and people require beter quality water, it is important to find an efficient and economic method to remove the nitrate nitrogen. In this thesis, a method of hydrogenotrophic denitrification ba- sed on bio-electrochemical reactor has been studied. The car- bon electrode is used as anode, and the cathode, which could be acted as the carrier for the bacteria, is activated carbon fiber. Water was electrolysed and gave off the hydrogen in the cat- hode, the denitrifying bacteria fixed in the cathode would ma- ke use of the hydrogen to process the hydrogenotrophic deni- trification. During the reaction, the bacteria could remove the nitrate nitrogen without organic carbon source. So this method had a lot of advantages like low cost, litle residual sludge and no secondary polution.

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为了确定硝化纤维(含氮量11.89%~13.5%)的热物性参数,进行热分析计算,揭示其反应动力学机制,采用激光闪射法和差示扫描量热法对含氮量12%的硝化纤维的热物性参数进行了测量。给出了其熔点以下25~140℃的热扩散率、比热容及热导率的数值。结果表明,随着温度的升高,比热容逐渐增大,而热导率和热扩散率有所减小,但变化幅度并不显著。在热分析计算时,这些参数可近似为一组平均值:c p=1.131 J·g-1·K-1,D=0.413 mm2·s-1,λ=0.142 W·m-1·K-1。
In order to obtain the thermal physical parameters of nitrocellulose (nitrogen content 11.89%~13.5%) to make the thermal analysis calculations and reveal the reaction dynamics mechanism, laser flash method and differential scanning calorimetric (DSC) method were used to measure the thermal physical parameters of nitrocellulose with nitrogen content 12%(NC(12%N)). The values of thermal diffusivity, specific heat capacity, and thermal conductivity were obtained at temperature ranging from 25℃to 140 ℃.Results show that with the increase of temperature, the specific heat capacity increases, while the thermal conductivity and thermal diffusivity decrease.But the changes are not obvious.So these parameters can be determinatal as:in the calculation of thermal analysis:cp =1.131 J? g-1? K-1 ,D=0.413 mm2? s-1 ,λ=0.142 W? m-1? K-1 .
硝化厌氧甲烷氧化(DAMO)过程可以由一种称为Methylomirabilis oxyfera的DAMO细菌在有或者没有DAMO古菌下完成.已经报道的DAMO过程的菌群富集时间长(一般需要7~18月),且DAMO体系反硝化速率低.利用中空纤维膜生物反应器(HFMB)提高甲烷的传质来试图实现快速启动DAMO反应,结果发现HFMB在不到3个月时间内就表现出DAMO反应,其反硝化速率达到50 mg·L-1·d-1硝酸盐氮.二代测序显示,HFMB中微生物以Anaerolineaceae,Azospira,CL500-3占绝对优势,分别为39.08%,13.68%和11.54%,而DAMO细菌(Methylomirabilis)和与厌氧甲烷氧化有关的古菌Methanosarcina分别占0.02%和0.13%,因此推测在HFMB中DAMO过程是由一群新的菌群主导完成.
The process of denitrifying anaerobic methane oxidation (DAMO) can be catalyzed by DAMO bacteria called Methylomirabilis oxyfera with or without the involvement of DAMO archaea .Enrichment of DAMO microbes often takes a long time (7 ~ 18 months) to show a faint denitrification function in reported DAMO process .This study aimed to fast enrich DAMO microbes in a hollow fiber membrane bioreactor (HFMB) as the special structure of hollow fiber can increase the mass transfer of methane .It is found that HFMB shows DAMO activity in a shorter period of time (<3 months) and the denitrificationrate reaches 50 mg · L -1 · d-1 NO3 -‐N .The next‐generation DNA sequencing on the microbes in HFMB shows that Anaerolineaceae ,Azospira,CL500‐3 are dominant with 39.08% ,13.68% and 11.54% of the total microbes , respectively . Meanwhile , Methylomirabilis (DAMO bacteria ) and Methanosarcina (DAMO archaea) are only 0.02% and 0.13% ,respectively .It is speculated therefore that the DAMO pro

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文章以硝酸盐溶液为阴极的电子受体,在阴极室中分别接种活性污泥混合菌和纯反硝化单菌株,构成生物阴极微生物燃料电池(microbial fuel cell ,简称MFC)A-MFC和B-MFC。实验结果表明:在外接电阻为100Ω情况下,A-MFC和B-M FC最大输出电压分别为119.6 mV和117.2 mV ,硝酸盐在B-M FC阴极室的平均反硝化速率为2.19 mg/(L&#183;d),比A-MFC中的平均反硝化速率1.86 mg/(L&#183;d)略高;扫描电镜观察到A-MFC和B-M FC的阴极碳布纤维丝表面形貌存在差异,A-MFC中碳布被孔状结构物覆盖,而B-M FC阴极碳布被片层状结构物所覆盖;同时发现A-MFC的阴极碳布循环伏安法CV曲线上均出现了明显的还原峰,表明A-MFC阴极碳布上的微生物进行了催化还原反应,而且阴极溶液均出现1对明显的氧化还原电对,说明阴极溶液中确实存在氧化还原介体进行微生物与电极间传递电子。
With the nitrate solution as the electron acceptor ,mixed bacteria from activated sludge and pure denitrifying bacteria were inoculated in the cathode chamber ,and two kinds of biocathode micro-bial fuel cells(MFCs) named A-MFC B-MFC were built .The experimental results showed that the maximum output voltages of A-MFC and B-MFC were 119.6 mV and 117.2 mV respectively when the external resistance was 100 Ω .The average denitrification rate in B-MFC was 2.19 mg/(L · d) and the average denitrification rate in A-MFC was 1.86 mg/(L · d) .The cathode carbon cloth surface morphology of A-MFC was different from that of B-MFC according to scanning electron microscope observation ,and the carbon cloth in A-MFC was covered by macroporous structure ,however the car-bon cloth in B-MFC was covered by lamellar structure .It was also found that there were an obvious reduction peak in the cyclic voltammetry(CV) curve of A-MFC cathode carbon cloth and an oxidation-reduction pair in the cath

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