苯胺在碱性溶液中的电化学聚合和聚合物的性质

苯胺在碱性溶液中电化学氧化时，阳极上形成深黄色的聚苯胺，其氧化峰电位为０．７Ｖ（ｖｓ．Ａｇ／ＡｇＣｌ含饱和ＫＣｌ溶液），比在酸性溶液中氧化约低０．３Ｖ，环一盘电极实验结果表明，在碱性溶液中，苯胺氧化时生成两种可溶性的中间物，形成的聚合物颜色不随电位和ｐＨ值而变化，在空气和碱性溶液中具有很高的稳定性，在紫外－可见光谱图上，聚合物的吸收峰出现在５００ｍ左右。     

食品中砷允许含量和人体容许摄入量

我国规定每公斤粮食中含砷量不应超过０．７毫克,食用植物油不超过０．１毫克,酱、味精、井盐、矿盐和冷饮食品均不应超过０．５毫克,酱油和醋每升不应超过０．４５毫克。 体内微量的砷对健康无甚影响,世界卫生组织暂定人体每日容许摄入量为：每公斤体重不超过０．０５毫克。砷的摄入量在此范围内是安全的。 近来有些报道还认为,砷是动物和人体的必需微量元素。据报道,均匀饮食极微量的砷可使人体强健,肌肤更光润白嫩。食品中砷允许含量和人体容许摄入量     

环氧化植物油的制备

天然油脂在无溶剂加压（约０．１５ＭＰａ）条件下，经甲酸（８５％）、双氧水（５０％）环氧化，一步合成增塑剂兼稳定剂环氧化油脂，得微黄色油状透明液体；环氧大豆油和环氧葵子油的环氧值均在６．２％～６．６％，环氧玉米油的环氧值６．０％～６．４％；碘值小于３ｍｇ／ｇ；精油转化率１０４％～１０８％。     

浅论绿茶与乌龙茶氟含量对人体健康的影响

分别用重蒸水和自来水，通过蒸煮法和浸泡法制出不同浓度的绿茶液和乌龙茶液，对比测定研究茶液中氟含量，结果表明，茶液中的氟含量随茶叶浓度增加而增加，且乌龙茶高于绿茶，当茶叶浓度超过１０．０ｇ／Ｌ时，茶液中的氟含量即超过国家饮水卫生标准，提示人们饮用水茶液浓度在５．０ｇ／Ｌ左右为宜。     

石墨炉原子吸收光谱法测定尿镉

采用磷酸作为基体改进剂，石墨炉原子吸收光谱法测定了尿镉，其检测限为０．０７μｇ／Ｌ，标准曲线线性范围０．０－５．０μｇ／Ｌ回收率９９．９１％，方法准确、简便、快速、污染少。     

β—环糊粗富集固相反射分光光度法测定钯

研究了用自制的β－环糊精交联聚合物树脂包结吸附，固相反射散射分光光度法对钯的测定。结果表明，最大吸收峰位于５７４ｎｍ处，钯含量在０～８μｇ／１０ｍＬ范围内，有良好的线性关系，检出限为１５μｇ／Ｌ，测定５μｇＰｄ１１次，其相对标准偏差为１．５５％。用于地质矿样分析，结果与推荐值相符。     

环境和生物样品中多来宝残留量的气相色谱分析方法研究

 湿性样品中的多来宝残留物用丙酮（水样和干样用石油醚）提取，提取液经石油醚再萃取、浓缩后，用被石油醚饱和的乙腈分配，过硅胶氧化铝混合柱净化，室温下与（ＣＨ３）３ＳｉＩ衍生化反应，生成３－苯氧基苄基碘，用ＧＣ检测。当添加浓度为０．０５，０．１０，１．００μｇ／ｇ时，样品的平均回收率为８０．７％～１１０．０％，方法最小检出量为０．０１ｎｇ，样品最小检出浓度是：水０．００１ｍｇ／Ｌ，稻米和土壤０．０１μｇ／ｇ，稻草、谷壳、水浮莲和罗非鱼为０．００８μｇ／ｇ。     

环境和生物样品中多来宝残留量的气相色谱分析方法研究

湿性样品中的多来宝残留物用丙酮（水样和干样用石油醚）提取，提取液经石油醚再萃取、浓缩后，用被石油醚饱和的乙腈分配，过硅胶氧化铝混合柱净化，室温下与（ＣＨ３）３ＳｉＩ衍生化反应，生成３－苯氧基苄基碘，用ＧＣ检测。当添加浓度为０．０５，０．１０，１．００μｇ／ｇ时，样品的平均回收率为８０．７％～１１０．０％，方法最小检出量为０．０１ｎｇ，样品最小检出浓度是：水０．００１ｍｇ／Ｌ，稻米和土壤０．０１μｇ／ｇ，稻草、谷壳、水浮莲和罗非鱼为０．００８μｇ／ｇ。     

焙烧富集分离—氢化物原子荧光法测定地质物料中痕量硒

本文研究了一种焙烧富集分离，氢化物－原子荧光法测定地质物料中痕量Ｓｅ方法。系统地了Ｓｅ富集分离条件，考查了３０多种元素在焙烧前后对测定Ｓｅ的影响。在选定的最佳实验条件下，方法检出下限为０．０１μｇ／ｇ和０．０８９μｇ／ｇ，线性范围０．００１－０．３μｇ／ｍＬ。样品中Ｓｅ含量水平为０．０３６μｇ／ｇ和０．０８９μｇ／ｇ时的测量精度（ＲＳＤ）分别为１０％和５．８％。加标回收率为９７－９９％。采用本方法     

饮料食品中Ge－132和Ge~（4＋）含量测定研究

本文报告了在０．０１ｍｏｌ／ＬＣＴＡＢ体系中，以Ｆ－为掩蔽剂、苯芴酮显色、用分光光度法测定饮料食品中Ｇｅ－１３２含量，最低检测限０．０５４μｇ／ｍＬ；线性范围０．５４～２７．１４μｇ／ｍＬ；回收率９６．３％～１０１．５％，并确定了Ｇｅ－１３２摩尔吸收系数（ε）３．３９×１０４。用本法测定了康寿茶、矿泉水和博士奶中Ｇｅ－１３２含量，灵敏度高、重现性和准确度好。用盐酸化本体系，研究了二氧化锗（Ｇｅ~（４＋））的含量测定，其最低检测限０．０２１μｇ／ｍＬ；线性范围１．０～２１．０μｇ／ｍｌ；回收率９５．８％～１０２．８％，Ｇｅ－１３２不干扰。饮料食品中同时存在Ｇｅ－１３２和Ｇｅ（４＋）时，本体系可分别测定两者含量。     

Evaluation of the Effect of Elite Jojoba Lines on the Chemical Properties of their Seed Oil

Jojoba oil (JO) extracted from seeds has outstanding properties, including anti-inflammatory, antioxidant, and antibacterial activities, and can be stored forlong periodsof time. The unique properties of jojoba oil depend on its chemical composition; therefore, the effect of the jojoba genotype on the chemical properties and active components of the seed oil was evaluated in this study. Oil samples were collected from 15 elite Egyptian jojoba lines. The chemical composition, such as moisture, crude fiber, crude oil, ash, and crude protein of elite lines’ seeds was determined to investigate the variation among them based on the jojoba genotype. In addition, the iodine value was obtained to measure the degree of jojoba oil unsaturation, whereas the peroxide number was determined as an indicator of the damage level in jojoba oil. Fatty acid composition was studied to compare elite jojoba lines. Fatty acid profiles varied significantly depending on the jojoba genotype. Gadoleic acid exhibited the highest percentage value (67.85–75.50%) in the extracted jojoba oil, followed by erucic acid (12.60–14.81%) and oleic acid (7.86–10.99%). The iodine value, peroxide number, and fatty acid composition of the tested elite jojoba lines were compared withthose reported by the International Jojoba Export Council (IJEC). The results showed that the chemical properties of jojoba oils varied significantly, depending on the jojoba genotype.     

Recovery Techniques Enabling Circular Chemistry from Wastewater

In an era where it becomes less and less accepted to just send waste to landfills and release wastewater into the environment without treatment, numerous initiatives are pursued to facilitate chemical production from waste. This includes microbial conversions of waste in digesters, and with this type of approach, a variety of chemicals can be produced. Typical for digestion systems is that the products are present only in (very) dilute amounts. For such productions to be technically and economically interesting to pursue, it is of key importance that effective product recovery strategies are being developed. In this review, we focus on the recovery of biologically produced carboxylic acids, including volatile fatty acids (VFAs), medium-chain carboxylic acids (MCCAs), long-chain dicarboxylic acids (LCDAs) being directly produced by microorganisms, and indirectly produced unsaturated short-chain acids (USCA), as well as polymers. Key recovery techniques for carboxylic acids in solution include liquid-liquid extraction, adsorption, and membrane separations. The route toward USCA is discussed, including their production by thermal treatment of intracellular polyhydroxyalkanoates (PHA) polymers and the downstream separations. Polymers included in this review are extracellular polymeric substances (EPS). Strategies for fractionation of the different fractions of EPS are discussed, aiming at the valorization of both polysaccharides and proteins. It is concluded that several separation strategies have the potential to further develop the wastewater valorization chains.     

On the direct reduction of arsonic acids to arsenoso compounds: mechanisms and preparations†

By using a variety of reducing agents, either alone or in the presence of iodide as a catalyst, the reduction of arsonic acids to arsenoso compounds and/or arsonous acids has been studied. The solvent and temperature are important for a clean reduction. The mechanism of the reduction involves prior protonation of the  AsO₃H₂ group, and can be rationalized in the framework of the ‘hard and soft acids and bases’ principle, which is used to predict other reducing systems and to explain other literature data. For preparative purposes, triphenylphosphine/iodine, hexamethylphosphorous triamide/iodine and ascorbic acid/iodine give flexibility of choice depending on the substrate. The first two of these systems decompose arsonic acids with a weak C–As bond but the last system is sufficiently mild towards the same arsonic acids. Copyright © 2000 John Wiley & Sons, Ltd.     

Sorption of cesium and strontium ions on hydrous titanium dioxide from chloride medium

Epiboron instrumental neutron activation analysis (EINAA) using flexible boron as thermal neutron filter, has been used to analyze several salt samples obtained from various markets in Ghana for iodine. The method involves the irradiation of samples in boron carbide-lined polyethylene vials at the outer irradiation site of the Ghana Research Reactor-1 (GHARR-1). The samples were then counted directly without any pre-treatment on a Canberra N-type HPGe detector. The qualitative and quantitative analyses were done using the 443 keV photopeak of ¹²⁸I. The precision and accuracy of the method have been evaluated and the detection limits of the various samples were calculated. The values of iodine determined in the iodized salt range between 10.0 and 210 ppm. For non-iodinated salts, iodine levels were below 500 ppb. The values obtained show great variations among the salt samples, sample collection time and from market to market. This results show that the method can be successfully applied in the determination of trace amount of iodine in salt samples without any chemical separation.     

Effect of iodine on small-angle X-ray diffraction from drawn poly(ethylene terephthalate) film

The effect of iodine sorption on the small-angle x-ray diffraction intensity is discussed in terms of the distribution of iodine sorbed in the amorphous regions of polymers. The change in the intensity of the peak corresponding to long periods is measured as a function of the iodine uptake in drawn, and annealed poly(ethylene terephthalate) films. A linear relation with slope K is observed between the square root of relative intensity and iodine uptake. The slope K varies with annealing conditions. Theoretical values calculated for models of the distribution of iodine in amorphous regions, are compared with the observed K. Results can be interpreted on the basis of a “concave” distribution of iodine, i.e., with sorption sites more numerous near a crystal surface than in the interior of an amorphous region.     

Ascorbic Acid/Iodine and Triphenylphosphine/Iodine as Reducing Agents for the As(V)[dbnd]O Group

The scope of ascorbic acid/iodine and triphenylphosphine/iodine in methanol for the direct reduction of arsenic(V) compounds having the As[dbnd]O group has been investigated. Ascorbic acid/iodine reduces arsonic acids, diphenylarsinic acid (but not dimethylarsinic acid), and triphenylarsine oxide. The rates of reduction depend on the electronic effects of the ligands bound to arsenic and on the hydrogen-bonding strength of the species, when present. When the As(V) compound has an [sbnd]NH ₂ or an [sbnd]NH ₃ ⁺ group, the reduction product reacts with a ketonic form of dehydroascorbic acid, giving condensation product(s). Triphenylphosphine/iodine reduced slowly the zwitterionic o-aminophenylarsonic acid but reduced faster the hydrochloric acid salt of the same acid. It reduced dimethylarsinic acid as well because the powerful electron-withdrawing Ph ₃ P ⁺coordinated to As[dbnd]O seems to outweigh the electronic and hydrogen bonding effects.     

Biodegradable polymers derived from natural fatty acids

A new class of polyanhydrides synthesized from nonlinear hydrophobic fatty acid esters, based on ricinoleic, maleic acid, and sebacic acid, possessed desired physico-chemical and mechanical properties for use as drug carriers. The polymers were synthesized by melt condensation to yield film-forming polymers with molecular weights exceeding 100,000. Their rate of elimination from rats in the course of about 2 months was faster than that found for similar polyanhydrides previously tested. In vitro studies showed that these polymers underwent rapid degradation in the first 10 days. The drug release followed first-order kinetics, showing a rapid drug release rate in the first 10 days which correlated with the degradation of the polymers. The fatty acid ester monomers underwent in vitro enzymatic degradation to the natural starting acids. Tests in rats demonstrated their toxicological inertness and biodegradability. © 1995 John Wiley & Sons, Inc.     

Analysis of Fatty Acids,Amino Acids and Volatile Profile of Apple By-Products by Gas Chromatography-Mass Spectrometry

Apple industrial by-products are a promising source of bioactive compounds with direct implications on human health. The main goal of the present work was to characterize the Jonathan and Golden Delicious by-products from their fatty acid, amino acid, and volatile aroma compounds’ point of view. GC-MS (gas chromatography-mass spectrometry) and ITEX/GC-MS methods were used for the by-products characterization. Linoleic and oleic were the main fatty acids identified in all samples, while palmitic and stearic acid were the representant of saturated ones. With respect to amino acids, from the essential group, isoleucine was the majority compound identified in JS (Jonathan skin) and GS (Golden skin) samples, lysine was the representant of JP (Jonathan pomace), and valine was mainly identified in GP (Golden pomace). A total number of 47 aroma volatile compounds were quantified in all samples, from which the esters groups ranged from 41.55–53.29%, aldehydes 29.75–43.99%, alcohols from 4.15 to 6.37%, ketones 4.14–5.72%, and the terpenes and terpenoids group reached values between 2.27% and 4.61%. Moreover, the by-products were valorized in biscuits manufacturing, highlighting their importance in enhancing the volatile aroma compounds, color, and sensorial analysis of the final baked goods.     

Synthesis,characterization, optical,thermal and electrical properties of polybenzimidazoles

The variation of dielectric constant and dielectric loss of two novel polybenzimidazole (PBI) were studied at constant temperature with variable frequency. The polymers have shown maximum dielectric constant at low applied frequency 50 Hz at 393 K due to the space charge polarization. The AC conductivity and activation energy of polymers were arrived from dielectric constant and dielectric loss values. PBIs were synthesized by the oxidative polycondensation of benzimidazole monomers, 2-(1H-benzo [d] imidazole-2-yl)-4-bromophenol (BIBP), and 2-(1H-benzo [d] imidazole-2-yl)-6-methoxyphenol (BIMP) in an aqueous alkaline medium using NaOCl as oxidant. The monomers and polymers were characterized by various spectroscopic techniques. Fluorescence spectra of monomers and polymers showed their λ _max emission in the region of 472–479 and 463–472 nm respectively. The electrical conductivities of iodine doped polybenzimidazoles were measured by four-point probe technique and it increases with increase in iodine vapour contact time. The electrical conductivity values were correlated with the charge density on imidazole nitrogen obtained from Huckel calculation method. Both the PBI are having reasonably good thermal stability and are shown by high carbines residues of around 40% at 500°C in thermogravimetric analysis.     

Synthesis and characterization of a new dyestuff polymer soluble in alkaline aqueous media

Novel dyestuff polymers were successfully obtained through oxidative polymerization technique. The synthesized Schiff base and its polymer were soluble in alkaline＇aqueous medium and they have various colors in different solutions. Also, it can be said that the synthesized compounds are suitable as coloring agent （dyestuff） for textile applications. Fluorescence properties of the compounds were determined in DMF with different concentrations （mg/L）. Poly-tris（4- aminophenyl）methanol （P-TAPM） has quite high emission and excitation intensity values. Optical and electrochemical band gaps of the polymers were lower than those of the monomers indicating the more conjugated structure of the polymers. The oxidized states of the novel dyestuff compounds were examined by cyclic voltammetry （CV） technique. The solid state conductivity measurements showed that the synthesized polymers were semiconductors when exposed to the iodine vapour their conductivities could be increased. P-TAPM had the highest undoped conductivity. Thermal characterizations of the synthesized compounds were carried out by TG-DTA and DSC methods.