Metabolites identification of oil palm roots infected with Ganoderma boninense using GC–MS-based metabolomics

An approach to metabolomics profiling of non-infected and Ganoderma boninense (G. boninsense) infected oil palm roots crude extracts that utilize gas chromatography-mass spectrometry (GC–MS) and multivariate statistics of principal component analysis (PCA) have been tested. This combination has provided a rapid approach in investigating the changes in the metabolite variations of non-infected and infected oil palm roots at 14 and 30 days post-infection. The extracts were prepared by using 80% (v/v) of methanol. In identifying the metabolites responsible for each differentiation, PCA model was generated in loading bi-plot. Dimethyl benzene-1,4-dicarboxylate, methyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate, ergost-5-en-3-ol, (3β), stigmast-5-en-3-ol, (3β), stigmasterol, methyl hexadecanoate, methyl (9Z,12Z)-octadeca-9,12-dienoate, methyl octadecanoate, 2-(hydroxymethyl)-2-nitropropane-1,3-diol, methyl (Z)-octadec-6-enoate and (E)-icos-5-ene were found more abundant in G. boninense infected roots than in non-infected roots. Steroidal compounds and fatty acid derivatives which has been determined in the non-infected and G. boninense infected roots regulate a variety of responses to the G. boninense. The abundant of these metabolites in G. boninense infected roots are due to the crucial roles in pathogen defence.     

Modelling of Dewatering and Desalting Processes for Large-capacity Oil Treatment Technology

This paper is devoted to analysis of oil treatment technology in the case of complex industrial process realization and further selection of technological mode. Mathematical modelling method is used to improve the efficiency of dewatering and desalting processes. The simulation system based on module modelling principle is developed. Every module is described in terms of appropriate combination of phenomena and processes. Problems of oil treatment analysis of complex structured technological scheme and searching of effective dewatering and desalting processes technological modes are solved.     

Investigation and optimization of the recovery of coal fines using oil agglomeration process: Use of waste oils from different sectors

The high cost of the bridging liquid subdues the implementation and commercialization of oil agglomeration process. To overcome this problem, waste oils from different sectors were used in this present study. The performance of the process was assessed based on the responses like ash rejection and organic matter recovery. The aim of the present study was to investigate the usage of waste oils from different sectors and to optimize and analyze the behavioral pattern showcased by different variables (pulp density, oil dosage, agglomeration time and oil type) using response surface methodology (Box-Behnken design). Experimental investigation shows that the optimum pulp density, oil dosage, agglomeration time and oil type condition obtained as 3%, 15%, 15?min and waste engine oil, respectively. At optimum condition, the % ash rejection and % organic matter recovery obtained as 63.94% and 81.8%, respectively.     

Gas chromatographic determination of carbonyl compounds in biological and oil samples by headspace single-drop microextraction with in-drop derivatisation

A suitable method for the gas chromatographic determination of 10 characteristic carbonyls in biological and oil samples based on the in-drop formation of hydrazones by using 2,4,6-trichlorophenylhydrazine (TCPH), has been developed. The derivatisation-extraction procedure was optimized separately for aqueous and oil samples with respect to the appropriate organic drop solvent, drop volume, in-drop TCPH concentration, sample stirring rate, temperature during single-drop microextraction (SDME), reaction time and headspace-to-sample volume ratio. The optimization showed differentiation of optimum values between the studied matrices. The limits of detection were found to range from 0.001 to 0.003 μg mL⁻¹ for the aqueous biological samples and from 0.06 to 0.20 μg mL⁻¹ for the oil samples. The limits of quantification were in the range of 0.003-0.010 μg mL⁻¹ and 0.020-0.059 μg mL⁻¹ for aqueous and oil samples, respectively. The overall relative standard deviations of the within-day repeatability and between-day reproducibility were <4.4% and <8.2% for the aqueous biological samples and <3.9% and <7.4% for the oxidized oil samples.     

Effect of weighting materials on carbonation of oil well cement-based composites under high temperature and CO2-rich environment

As an indispensable part of cement slurry for high temperature and high pressure oil and gas wells, weighting materials have a significant impact on the carbon dioxide corrosion of oil well cement-based composites.This paper studied the carbonation process of cement with three weighting agents, and evaluated the compressive strength and carbonation depth of cement at 150 ℃. XRD, SEM and MIP were used to study the carbonation mechanism of cement. When 21 days of carbonation, the carbonation depth growth rate of hausmannite cement was 0.21 mm/d, hematite cement was 0.24 mm/d, and barite cement was 0.31 mm/d. The compressive strength of cement decreased after carbonation,and the carbonation had a minor influence on the compressive strength of hausmannite cement and the most significant impact on barite cement. The carbonation product of oil well cement was mainly calcite. Unstable vaterite mainly existed in the barite cement sample, indicating that the barite cement sample was the most serious corrosion. In the carbonation zone, the number of pores smaller than 10 nm increased the most in the hausmannite cement sample. Pores with a diameter greater than 100 nm accounted for 1.9 % in the hausmannite cement, 3.0 % in hematite cement, and 4.8 % in barite cement. The result shows that hausmannite is the most conducive to the corrosion resistance of oil well cement.     

Non-linear mechanical behaviour and bio-composite modelling of oil palm mesocarp fibres

Understanding the non-linear mechanical behaviour of oil palm mesocarp fibres (OPMF) is important for bio-composite application. The mechanical characterisation of this fibre is challenging due to the microstructure of the fibres consisting of silica bodies on the surface and cellular structures within the cross section. In this work, we proposed a constitutive material model for OPMF by including a stress-softening function into the large strain viscoelastic model. The model shows agreement with loading–unloading and stress relaxation tensile tests. The model was then used for micro-scale finite element modelling of the fibre–silica body–matrix (resin) interface to simulate sliding of a bio-composite material. A multi-particles model was also developed to check the effect of the constitutive model towards the mechanics of a bio-composite system. Modelling results suggested that under the micro-scale level (~50 μm), silica body plays a major role in improving the mechanical behaviour of the bio-composite system. On the other hand, under the macro-scale level (~0.18 mm), a single fibre model is sufficient to simulate a bio-composite multi-fibres material.     

Fast and effective low‐temperature freezing extraction technique to determine organotin compounds in edible vegetable oil

Most organotin compounds that have been widely used in food packaging materials and production process show serious toxicity effects to human health. In this study, a simple and low‐cost method based on high‐performance liquid chromatography with inductively coupled plasma mass spectrometry for the simultaneous determination of four organotins in edible vegetable oil samples was developed. Four organotins including dibutyltin dichloride, tributyltin chloride, diphenyltin dichloride, and triphenyltin chloride were simultaneously extracted with methanol using the low‐temperature precipitation process. After being concentrated, the extracts were purified by matrix solid‐phase dispersion using graphitized carbon black. The experimental parameters such as extraction solvent and clean‐up material were optimized. To evaluate the accuracy of the new method, the recoveries were investigated. In addition, a liquid chromatography with tandem mass spectrometry method was also proposed for comparison. The procedures of extracting and purifying samples for the analysis were simple and easy to perform batch operations, also showed good efficiency with lower relative standard deviation. The limits of detection of the four organotins were 0.28–0.59 μg/L, and the limits of quantification of the four organotins were 0.93–1.8 μg/L, respectively. The proposed method was successfully applied to the simultaneous analysis of the four organotins in edible vegetable oil. Some analytes were detected at the level of 2.5–28.8 μg/kg.     

聚偏氟乙烯接枝甲基丙烯酸甲酯油水分离膜的研究

使用四乙基氢氧化铵(TEAH)液相本体改性聚偏氟乙烯(PVDF),以过氧化苯甲酰(BPO)为引发剂,将甲基丙烯酸甲酯(MMA)接枝到改性PVDF骨架上,合成聚偏氟乙烯接枝聚甲基丙烯酸甲酯(PVDF-gPMMA)共聚物,通过浸没沉淀法制备PVDF-g-PMMA亲水性油水分离膜.通过傅里叶红外光谱(FTIR)、扫描电镜(SEM)和过滤试验分析了膜的结构和性能.同时研究了TEAH浓度和改性时间对PVDF-g-PMMA膜表面接触角的影响.结果表明,TEAH使PVDF脱去HF产生碳碳双键且MMA成功接枝到改性的PVDF骨架上,膜内外孔隙分布均匀;PVDF-g-PMMA膜的接触角随着TEAH浓度的增加、改性时间的加长而减小.TEAH浓度为2.0 wt%,改性20 min制备的PVDF-g-PMMA膜,接枝率为27.1%,孔隙度为71.6%,平均孔径为78.9 nm,接触角降至55.9°,且在50 s内降为0;纯水通量提高到665.34 L/(m2·h),截留率和水通量恢复率分别达到95.6%和90.1%.与纯PVDF膜相比,PVDF-g-PMMA膜的分离性能显著提高.     

Tensile Properties and Morphology of Oil Palm Empty Fruit Bunch Regenerated Cellulose Biocomposite Films

The regenerated cellulose (RC)biocomposite films were prepared using casting method where oil palm empty fruit bunch (OPEFB) and microcrystalline cellulose (MCC) were dissolved in N-dimethylacetamide/lithium chloride (DMAc/LiCl)solution. The increasing of OPEFB contents up to 2 wt% increased the tensile strength and modulus of elasticity of RC biocomposite films while the elongation at break decreased. However, at 3 and 4 wt% of OPEFB content, the tensile strength and modulus of elasticity decreased with increases OPEFB content, but elongation at break increased. The increment of tensile strength and modulus of elasticity at 2 wt% is due to the OPEFB fiber that partially dissolved and dispersed with the OPEFB matrix. The morphology studies illustrate that at 2 wt% of OPEFB content of biocomposite films surface consists less voids and agglomerations than at 4 wt%. This can be considered the RC filler was partially dispersed with the RC matrix in the biocomposite films.     

大口径离轴凸非球面的加工和检测

将光学系统波像差检验技术与子孔径拼接测试技术相融合提出了凸非球面系统拼接检测方法,对该方法的原理和实现步骤进行了分析和研究,并建立了合理的子孔径拼接数学模型.依次利用计算机控制光学表面成形技术和磁流变抛光技术对一包含大口径凸非球面的离轴三反光学系统的各反射镜进行加工,并对整个系统进行装调和测试.测定光学系统各视场的波像差分布,通过综合优化子孔径拼接算法和全口径面形数据插值求解得到大口径凸非球面全口径的面形信息.结合工程实例,对一口径为292mm×183 mm的离轴非球面次镜进行了系统拼接测试和加工,其最终面形分布的均方根值为0.017λ(λ=632.8 nm).