一种植物油中苯并（a）芘含量测定的固相萃取前处理方法

为了建立一种准确性高、成本低的植物油中苯并(a)芘测定的样品前处理方法，基于GB 5009.7—2016以自制氧化铝柱为固相萃取柱，采用单因素试验对称样量、洗脱剂量、洗脱流速、吸附剂存放时间、吸附剂量这5个影响植物油中苯并（a）芘洗脱的因素进行研究，优化前处理条件，并对测定方法进行考察。结果表明：优化的前处理条件为称样量0.100 0 g、洗脱剂量120 mL、吸附剂（氧化铝）量22 g、洗脱流速1滴/2 s、吸附剂存放时间少于12周；方法检出限为0.2 μg/L，样品加标回收率为94.23%～100.00%，RSD为1.20%～7.36%；同一样品测定结果与SGS测定值接近，相对平均偏差为2.36%～3.50%。说明本试验方法测定结果准确，可应用于油脂企业植物油中痕量苯并（a）芘的测定。     

Synthesis and characterization of SrFeOx hetero-film resistance-switching device with low operation voltage

As a critical topological phase transition material, SrFeO_x could play an essential role in the field of resistive memory. How to implement resistance-switching more softly and ensure the stability of materials has always been a relevant research hotspot. Regulating the oxygen environment during the deposition process of the films can effectively control the stoichiometry of the functional layer and then improve the resistance-switching characteristics of the device. In this paper, a SrFeO_x hetero-film was prepared by oxygen pretreatment on the SrRuO₃ surface before SrFeO_x deposition, and the as-assembled micrometer-scale device exhibits a low set operating voltage of 0.6 V and favorable cycling characteristics. The SrFeO_x hetero-film reveals a vertical brownmillerite superlattice-like structure with ～20 nm perovskite buffer layer, which benefits the connection and rupture of conductive filament. Additionally, XPS and UV–vis were used to analyze the bonding energy and band gap of SrFeO_x hetero-film, and offers the experimental basis for the explanation of the conductive mechanism. Therefore, the device based on SrFeO_x hetero-film with low operation voltage provides a reference for low power consumption research on topological phase transition material.     

Improvement of thermal,microwave and ultrasonication pretreatment on the production of antioxidant peptides from sweet potato protein via in vitro gastrointestinal digestion

Effects of thermal (boiling, steaming and autoclaving), microwave and ultrasonication pretreatments on the production of sweet potato protein hydrolysates (SPPH) through in vitro gastrointestinal digestion (GID) were investigated. All pretreatments significantly increased the degree of hydrolysis (DH), antioxidant activities and molecular weight (MW) <3 kDa peptide fractions contents of SPPH in the order of autoclaving > microwave, steaming > boiling > ultrasonication (P < 0.05). Correlation analysis between peptides content and antioxidant activity suggested that antioxidant activity of SPPH mainly attributed to MW <3 kDa peptides. Diverse peptides ranged from 487.24 to 1477.74 Da with 7–13 amino acids were identified in the MW <3 kDa peptides fraction with autoclaving pretreatment and matched sporamins A, A precursor and B sequences from LC–QTOF–MS/MS analysis. Conformational structures of nine peptides were predicted with well-known antioxidant amino acids. There is a high potential for SPPH used as a functional supplement in food system.     

离子色谱-电导法检测酱油中氯化钠的含量

该研究采用灰化预处理+离子色谱-电导法检测酱油中食盐的含量，并与莫尔法、电位滴定法进行比较。结果表明，莫尔法存在滴定过量问题，电位滴定法对温度等外界环境条件和仪器操作要求苛刻，而离子色谱-电导法具有操作简便快速并具有较好的准确度和精密度。实验结果表明，氯化钠含量处于11.56～11.61 g/100 mL之间，回收率实验结果为96.00%～102.10%，相对标准偏差为0.089%。干扰实验对结果无明显影响，且能同时测定多种离子，可用于成品酱油中氯化钠含量的检验。     

汽车涂装废水处理技术的研究进展

汽车涂装中产生大量的工业废水，主要包括脱脂废水、磷化废水、电泳废水和喷漆废水等,其典型污染物为重金属离子、表面活性剂、油漆颗粒、磷酸盐等，是一类复杂及难处理的高浓度工业废水。依据废水中所含污染物的不同，对涂装各工序废水进行分质预处理可有效地去除磷酸盐、重金属离子、悬浮固体、油类物质等污染物，有利于减轻后续生物或高级处理单元的负荷，提高整个处理系统的效率。本文综述近年来汽车涂装废水处理方面的研究成果或实践，旨在总结预处理工艺及主体处理工艺的优点及存在的不足，希望为汽车涂装废水处理达标排放及循环回用提供一些借鉴。     

微波耦合铁碳微电解预处理石化废水的试验

采用微波耦合铁碳微电解技术对石化废水进行预处理,并对预处理前后水样中有机物的变化进行分析。结果表明,原水CODCr为10 500 mg/L,在废水pH值为3、铁碳投加量为20%、微波功率为700 W,经微波辐射5 min处理后,出水CODCr为2 370 mg/L左右,COD去除率稳定在77%左右,提高了废水的可生化性。GC-MS和三维荧光分析结果均表明,微波耦合铁碳微电解处理后,试验废水中有机物的数量及浓度大幅降低。结合后续生化处理,可以达到三级污水综合排放标准(GB 8978-1996)。微波耦合铁碳微电解可作为石化废水的有效预处理方法。     

甘油预处理蔗渣的木质素分离提取及结构表征

以甘油分别对甘蔗渣进行常压甘油自催化（AGO）预处理和常压甘油碱催化（al-AGO）预处理。利用酸沉法分别从预处理液中得到自催化甘油木质素（AGOL）和碱催化甘油木质素（al-AGOL）。利用单因素实验和正交实验得到最佳木质素提取工艺为转速8000r/min、离心时间15min、甘油混合液pH为3、甘油混合液浓度10%，在该条件下木质素AGOL和al-AGOL提取率分别达到72%和76%。采用扫描电镜（SEM）、元素分析、紫外光谱（UV）、凝胶色谱（GPC）、核磁共振¹H谱、热重分析以及抗氧化活性分析等技术手段对提取得到的木质素进行结构表征。结果表明：从甘蔗渣中提取的球磨甘蔗木质素（MBL）、AGOL和al-AGOL主要呈现出球形特征；AGOL和al-AGOL具有相似的活性特点，与MBL相比，AGOL和al-AGOL的分子量更小、分布更窄、均一性更好，热稳定性和抗氧化活性更高，有望成为重要的工业原料。     

Insights into biological delignification of rice straw by Trametes hirsuta and Myrothecium roridum and comparison of saccharification yields with dilute acid pretreatment

Rice straw is the most abundant agricultural residue on a global scale and is widely available as feedstock for cellulosic fuel production. However, it is highly recalcitrant to biochemical deconstruction and also generates inhibitors that affect enzymatic saccharification. Rice straw from eastern Arkansas was subjected to dilute acid pretreatment (160 °C, 48 min and 1.0% sulfuric acid) and solid-state fermentation with two lignocellulolytic fungi, Trametes hirsuta and Myrothecium roridum, and their saccharification efficacies were compared. T. hirsuta and M. roridum were tested separately; pretreatment of rice straw with either strain for seven days resulted in 19 and 70% enrichment of its holocellulose content, respectively. However, liquid chromatography analysis of the alkali extracts showed significant differences in cell wall degradation by T. hirsuta and M. roridum. T. hirsuta removed 15% more phenolic compounds and 38% more glucan than M. roridum, while M. roridum removed 77% more xylan than T. hirsuta. Fungal and dilute acid pretreated biomass was then hydrolyzed using Accellerase^® 1500, a saccharification cocktail. Saccharification efficiency of M. roridum was 37% higher than that of dilute acid pretreatment of rice straw, requiring 8% lower enzyme loading and 50% shorter enzymatic hydrolysis duration. Alkali extraction of fungal pretreated biomass also yielded 10–15 g kg⁻¹ of acid precipitable polymeric lignin (APPL), which is a valuable co-product for biorefineries. In comparison to dilute acid pretreatment, fungal pretreatment could be a cost-effective alternative for the degradation of recalcitrant biomass, such as rice straw.     

Improvement of corrosion protective performance of organic coating on low carbon steel by PEO pretreatment

Employing pretreatment is a pressing need for preparing anticorrosive coatings on carbon steels. However, conventional pretreatments are usually based on Cr, P and some other toxic elements, which are harmful to human body. For this reason, green and environmental techniques attract more and more attention. In this paper, plasma electrolytic oxidation (PEO) process was used as a pretreatment to fabricate an underlayer for the organic coating on low carbon steel. The anticorrosive performance of the organic coated samples with and without PEO pretreatment was studied by potentiodynamic polarization, ac/dc/ac electrochemical impedance spectroscopy, salt spray and immersion tests, respectively. Results show that the PEO process produces an oxide layer with porous and rough surface structure on the low carbon steel substrate. The porous and rough PEO layer is beneficial for enhancing the adhesion strength and thickness of the organic topcoatings. The organic coated sample with PEO pretreatment exhibits improved corrosion resistance and longer service life in corrosive environment compared to that without PEO pretreatment.