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1.
In this study, parenchyma cellulose, which was extracted from maize stalk pith as an abundant source of agricultural residues, was applied for preparing cellulose nanoparticles (CNPs) via an ultrasound-assisted etherification and a subsequent sonication process. The ultrasonic-assisted treatment greatly improved the modification of the pith cellulose with glycidyltrimethylammonium chloride, leading to a partial increase in the dissolubility of the as-obtained product and thus disintegration of sheet-like cellulose into nanoparticles. While the formation of CNPs by ultrasonication was largely dependent on the cellulose consistency in the cationic-modified system. Under the condition of 25% cellulose consistency, the longer sono-treated duration yielded a more stable and dispersible suspension of CNP due to its higher zeta potential. Degree of substitution and FT-IR analyses indicated that quaternary ammonium salts were grafted onto hydroxyl groups of cellulose chain. SEM and TEM images exhibited the CNP to have spherical morphology with an average dimeter from 15 to 55 nm. XRD investigation revealed that CNPs consisted mainly of a crystalline cellulose Ι structure, and they had a lower crystallinity than the starting cellulose. Moreover, thermogravimetric results illustrated the thermal resistance of the CNPs was lower than the pith cellulose. The optimal CNP with highly cationic charges, good stability and acceptable thermostability might be considered as one of the alternatively renewable reinforcement additives for nanocomposite production.  相似文献   
2.
INTRODUCTIONToday, the world's industry is utilizing less than 10% of biomass of raw materials from plantation [1]. Agricultural residues, such as cereal straws are important and abundant renewable organic resources of energy and production of a diversity of chemicals, including ethanol production [2], activated carbon [3] and ion exchangers [4]. Many other applications for Cereal straws are in the process of being developed.In china, wheat, maize and sorghum are the three major crops, w…  相似文献   
3.
A new sample business survey for agriculture, the REA survey, and a project of integration with the FADN network (RICA in Italy) have significantly changed the production of statistical information nowadays available with reference to the agricultural sector. On the basis of this relevant information, new economic analyses are being developed on farms’ performance, agricultural households’ income and the Common Agricultural Policy (CAP). In this paper the authors estimate the relationship between the levels of variables of interest and their sampling errors using models in order to improve the accessibility of the information on estimates accuracy to the final users (agricultural analysts, policy makers). The paper is the result of a joint research of the three authors. Sections 1–3 and 6 by Pizzoli, Sects. 4 and 5 by Rondinelli, Sect. 7 by Filiberti, conclusions joint to the three authors.  相似文献   
4.
This Review discusses the synthesis and characterization by our Group of new antibiotics belonging to the class of penicillins, cephalosporins and rifamycins with ferrocenyl and 1, 1′-ferrocenilene residues in the molecule. As reactants for 6-aminopenicillanic acid (6-APA) and 7-aminocephalosporanic acid (7-ACA) the following were used: 1, 1-bis(chlorocarbonyl)ferrocene, ferrocenyl sulfochloride, 1, 1′-ferrocenylenedisulfochloride and thioglycolic acids S-modified with ferrocene. In the synthesis of rifamycins, the hydrazides of the thioglycolic acids, S-modified with ferrocene, were employed as nucleophilic agents. The synthesized intermediates were characterized by elemental analysis, TLC, IR, UV and 1H NMR spectra. The characterization of new antibiotics was made by TLC, IR and UV spectral analysis. Biological activity was tested on Gram-negative and Gram-positive bacteria. Good activity is reported towards Gram-positive bacteria in the case of derivatives containing residues of thioglycolic acid S-modified with ferrocene, the antibacterial activity being similar to that of amoxicillin, carbenicillin and cephalothin. All compounds are inactive towards Gram-negative bacteria.  相似文献   
5.
Many natural products contain carbohydrate moieties that contribute to their biological activity. Manipulation of the carbohydrate domain of natural products through multiple glycosylations to identify new derivatives with novel biological activities has been a difficult and impractical process. We report a practical one‐pot enzymatic approach with regeneration of cosubstrates to synthesize analogues of vancomycin that contain an N‐alkyl glucosamine, which exhibited marked improvement in antibiotic activity against a vancomycin‐resistant strain of Enterococcus.  相似文献   
6.
本文综述了农业机械化投资行为的一般理论,探讨了影响农业机械化投资行为的内外部环境因素,研究了农业机械化投资行为的形成机制及其演变过程,并结合实际情况提出了农业机械化投资行为不平衡性的一般规律。  相似文献   
7.
泡沫分离,带溶剂萃取和沉淀法提取庆大霉素   总被引:1,自引:0,他引:1  
研究了用文题法从水相中分离砂大霉素的各种操作因素对分离过程的影响。在最适条件下,种方法对庆大霉素配制液的收率分别为72%,88%,87%,无机盐能使沉淀收率提高。将上述3法用于发酵液时,泡沫法和萃取法的收率均有显著降低,而沉淀法依然能达到很高的收率,ψ=捍沉淀率约为100%.  相似文献   
8.
在现有方法基础上对沉积物中磺胺类、喹诺酮类、大环内脂类和四环素类抗生素的提取、富集、净化以及仪器分析方法进行了优化。以EDTA-Mcllvaine缓冲溶液与乙腈(V:V,1:1)混合液作为提取液,利用超声波细胞破碎仪进行超声提取,串联强阴离子交换柱(SAX)和HLB固相萃取柱进行固相萃取(SPE),通过超高效液相/串联质谱(UPLC-MS/MS)测定沉积物中抗生素的含量。抗生素基质加标回收率在56.4%~110%,相对标准偏差为1.1%~24.3%,方法检出限0.0055~0.716 ng/g。本方法有效地提高了沉积物中抗生素的提取效率,并应用于实际样品的测定中。  相似文献   
9.
建立了固相萃取-高效液相色谱-串联质谱(SPE-HPLC-MS/MS)同时检测表层水中5类40种抗生素的分析方法。水样经过滤、固相萃取柱富集净化后,以乙腈-0.2%(v/v)甲酸水溶液为流动相进行梯度洗脱,采用电喷雾电离源,在多反应监测、正离子模式进行定性定量分析。结果显示,40种抗生素在1~200 μg/L水平下线性关系良好,平均加标回收率为41.3%~112.6%。采用该方法对长江南京段表层水体进行检测,共检出13种抗生素,含量为13.4~780.5 ng/L,其中喹诺酮类抗生素恩诺沙星检出率达100%,大环内酯类抗生素克林霉素最高检出水平达739.4 ng/L。该法高效、灵敏、可靠,可用于实际水样中多种抗生素的分析。  相似文献   
10.
Yuan L  Wei H  Li SF 《Electrophoresis》2005,26(1):196-201
A simple and fast method was developed to determine non-UV active compounds directly without derivatization. The usefulness of the method was demonstrated by detecting the major components in aminoglycoside antibiotic mixtures using capillary zone electrophoresis with potential gradient detection. Under optimized separation conditions (0.2 mM cetyltrimethylammonium bromide (CTAB), 1 mM ammonium citrate, pH 3.5), gentamicin was separated into three major peaks (C1, C1a, and C2+C2a) within 15 min. This method showed better sensitivity than other capillary electrophoresis (CE) methods for determining underivatized gentamicin. The linear range was from 10 to 500 ppm. Because of its good repeatability and simplicity, this new method could be a good alternative for the current assays given by US Pharmacopoeia and European Pharmacopoeia.  相似文献   
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