An Efficient Extraction-Free Method for Oxidative Desulfurization of Model Fuels Employing Cross-Linked Polyionic Liquid Phosphotungstate Catalysts

An efficient extraction-free oxidative desulfurization(ODS)process using a series of cross-linked polyionic liquid phosphotungstate(CLPIL-PW)catalysts is reported.The cross-linked PILs were prepared with DVB and 1-n-alkyl-3-vinyl imidazole hydrobromide(alkyl=ethyl,butyl,octyl,dodecyl),and were then assembled with phosphotungstic acid(H_(3)PW_(12)O_(40))to form the catalysts.The CLPIL-PWs have been applied to the oxidative removal of dibenzothiophene(DBT)from model oil with H_(2)O_(2) as an oxidant.The effects of ionic liquid(IL)cationic species,varying the DVB/IL molar ratio in the polymerization process,and varying operating conditions were investigated.The CLPIL-PWs were characterized by inductively coupled plasma(ICP)mass spectrometry,elemental analysis,scanning electron microscopy(SEM),Fourier transform infra-red(FTIR)spectroscopy,X-ray diffraction(XRD),^(13)C and^(31)P nuclear magnetic resonance(NMR)spectroscopy.The polydivinylbenzene-co-1-n-octyl-3-vinyl imidazole phosphotungstate(P(DVB-OVIm)PW)exhibited the highest DBT removal efficiency(99.9%)and remarkable recyclability,and could be reused eight times without reducing its activity.Finally,an extraction-free ODS mechanism is proposed.

Insights into the swelling process and drug release mechanisms from cross-linked pectin/high amylose starch matrices

Cross-linked pectin/high amylose mixtures were evaluated as a new excipient for matrix tablets formulations,since the mixing of polymers and cross-linking reaction represent rational tools to reach materials with modulated and specific properties that meet specific therapeutic needs.Objective:In this work the influence of polymer ratio and cross-linking process on the swelling and the mechanism driving the drug release from swellable matrix tablets prepared with this excipient was investigated.Methods:Cross-linked samples were characterized by their micromeritic properties(size and shape,density,angle of repose and flow rate)and liquid uptake ability.Matrix tablets were evaluated according their physical properties and the drug release rates and mechanisms were also investigated.Results:Cross-linked samples demonstrated size homogeneity and irregular shape,with liquid uptake ability insensible to pH.Cross-linking process of samples allowed the control of drug release rates and the drug release mechanism was influenced by both polymer ratio and cross-linking process.The drug release of samples with minor proportion of pectin was driven by an anomalous transport and the increase of the pectin proportion contributed to the erosion of the matrix.Conclusion:The cross-linked mixtures of high amylose and pectin showed a suitable excipient for slowing the drug release rates.

Nephelometric Performance Evaluation of Oxidized Starch in the Treatment of Coal Washery Effluent

This study investigated the coag-flocculation performance of oxidized starch coagulant (OSC) and its blends with alum and FeCl3 in removing turbidity from coal washery effluent at room temperature. A conventional laboratory bench-scale jar test apparatus was employed for the experiments. Coag-flocculation parameters such as reaction order α, rate constant K, coagulation time τ, etc. were determined. The optimum pH was observed at 4.0, while the blend of 30.0 mg/L FeCl3 and 250.0 mg/L OSC achieved the optimum turbidity removal. Turbidity removal efficiency was recorded between 96.0% and 99.9% for various dosages and pH studied. The coagulation rate constants, K recorded range from 9.393 × 10-5 L/mg.min to 8.294 × 10-1 min-1, while coagulation periods τ, range from 3.8 s to 235.7 s for various dosages and pH studied. The use of OSC blended with FeCl3 showed high level of efficiency, for the treatment of coal washery effluent.

An industrialized preparation technique of oxidized corn starch

An industrialized technique of preparation for oxidized com starch using oxygen as oxidant was investigated in this paper. The industrialized preparation parameters were optimized as follows： reaction temperature 85-95 ℃, oxygen flow rate 8-12 L/min, reaction time 210 min, the ratio of starch to water 1：5, 3.5 wt% of NaOH and 0.1 wt% of catalyst. The experimental results show that the concentration of hydrolysate-oxidaton product is 16-18 wt%. The powdered products were gained through dehydrated and powdered process using quadruple-effect evaporator, spray drying tower and guide shell mixer. The composting test indicates that the degradability of the oxidized corn starch can reach 76.4%. The complexation capacity of calcium ions reaches 108.5 mg per gram oxidized starch, and the detergency ratio （P） reaches 1.30 as builder.

A Facile Route for the Large Scale Fabrication of Graphene Oxide Papers and Their Mechanical Enhancement by Cross-linking with Glutaraldehyde

A facile route for the large scale production of graphene oxide(GO) papers and their mechanical enhancement has been presented in this work. The novel paper-like GO made from individual GO sheets in aqueous suspension can be achieved in large scale by a simple drop casting method on hydrophobic substrates.Significant enhancement in mechanical stiffness(341%) and fracture strength(234%) of GO paper have been achieved upon modification with a small amount(less than 10 wt%) of glutaraldehyde(GA). The cross-linking reaction takes place between hydroxyl groups on the surface of GO and aldehyde groups of GA, through forming hemiacetal structure, which can result in distinct mechanical enhancement of the GO papers.

Study on Various Compositions of Polyvinyl Alcohol and Starch Blends by Cross-Linking with Glyoxal

The aim of this study is to analyze the various compositions of polyvinyl alcohol (PVA) and starch blends. The blends have been cross-linked with glyoxal to enhance its properties. The hydroxyl groups of PVA and starch react with glyoxal via formation of acetal bonds;hence crosslinking could take place. The cross-linking of glyoxal is observed in various analytical methods such as DSC and FTIR. The cross-linked blends showed better thermal and mechanical properties. Viscosity, tensile shear strength, pencil hardness and ultimate stress were evaluated to estimate the changes due to cross-linking. It was observed that the cross-linking is directly proportional to starch, since the starch hydroxyl groups are easily accessible for reacting. The cross-linked blend showed better cohesion between its chains, thereby increasing glass transition temperature. It was reflected in the subsequent increase in tensile strength properties.

Cross-linked polyelectrolyte reinforced SnO_(2)electron transport layer for robust flexible perovskite solar cells

SnO_(2)electron transport layer(ETL)is a vital component in perovskite solar cells(PSCs),due to its excellent photoelectric properties and facile fabrication process.In this study,we synthesized a water-soluble and adhesive polyelectrolyte with ethanolamine(EA)and poly-acrylic acid(PAA).The linear PAA was crosslinked by EA,forming a 3D network that stabilized the SnO_(2)nanoparticle dispersion.An organic–inorganic hybrid ETL is developed by introducing the cross-linked PAA-EA into SnO_(2)ETL,which prevents nano particle agglomeration and facilitates uniform SnO_(2)film formation with fewer defects.Additionally,the PAA-EA-modified SnO_(2)facilitated a uniform and compact perovskite film,enhancing the interface contact and carrier transport.Consequently,the PAA-EA-modified PSCs exhibited excellent PCE of 24.34%and 22.88%with high reproducibility for areas of 0.045 and 1.00 cm~2,respectively.Notably,owing to structure reinforce effect of PAA-EA in SnO_(2)ETL,flexible device demonstrated an impressive PCE of 23.34%while maintaining 90.1%of the initial PCE after 10,000 bending cycles with a bending radius of 5 mm.This successful approach of polyelectrolyte reinforced hybrid organic–inorganic ETL displays great potential for flexible,large-area PSCs application.

Cross-Linking of Sago Starch with Furan and Bismaleimide via the Diels-Alder Reaction

This research paper describes the synthesis of thermo-reversible cross-linking of sago starch by grafting a furan pendant group(methyl 2-furoate)onto the starch backbone,followed by a Diels-Alder(DA)reaction of the furan functional group with 1,1′-(methylenedi-4,1-phenylene)bismaleimide(BM).The proof of principles was provided by FTIR and 1H-NMR analyses.The relevant FTIR peaks are the carbonyl peak(υC=O sym)at 1721 cm^(−1);the two peaks appeared after DA cross-linking,i.e.,at 1510 cm^(−1)(corresponding toυCH=CH BM aromatic rings,stretching vibrations),and at 1173 cm^(−1)(assigned to cycloadduct(C-O-C,δDA ring))while the^(1)H-NMR result shows evidence for the presence of a furan ring in the starch matrices(in the range ofδ6.3-7.5 ppm).The crosslinked starch product is indeed thermally reversible,as is evident from the appearance of exothermal(DA,temperature range of 50℃-70℃)and endothermal(retro DA,temperature range of 125℃-150℃)transitions in the DSC thermograms.This paper not only proves the thermal reversibility but also demonstrates that the final product properties(chemical,morphology,and thermal stability)can be tuned by varying the annealing temperature,BM intake,and reaction time.

5-Hexylidene-4-propylamino-1,5-dihydroimidazol-2-one formed from Cu-catalyzed oxidation with implication for the structure of a His-Lys cross-link

Cu-catalyzed oxidation of 5-hexyl-1,3-dihydroimidazo-2-one (1) in the presence of propylamine, as surrogates for the oxidized His side chain and Lys side chain, was investigated. 5-Hexylidene-4-propylamino-1,5-dihydroimidazol-2-one (2), a model His-Lys cross-link product, was isolated and structurally characterized by NMR and mass spectrometry.

Cross-linkedα-amylase aggregates on Fe3O4 magnetic nanoparticles modified with polydopamine/polyethyleneimine for efficient hydrolysis of starch

In this workα-amylase was immobilized on magnetic Fe3O4 nanoparticles with polyethylenimine(PEI)/polydopamine(PDA)coating or 3-aminopropyl triethoxysilane(APTES)for the first time via adsorption–precipitation–cross-linking.Compared with the freeα-amylase,the resultant magnetic cross-linkedα-amylase aggregates(PEI/PDA-M-CLEAs and N-M-CLEAs)exhibited excellent thermal and storage stability as well as pH stability.After storage at 25°C for 60 days,freeα-amylase only retained 60%of its initial activity,while PEI/PDA-M-CLEAs and N-M-CLEAs retained 80%and 78%of their initial activities,respectively.Furthermore,N-M-CLEAs and PEI/PDA-M-CLEAs showed good reusability.After 6 repeated uses,PEI/PDA-M-CLEAs and N-M-CLEAs still maintained 65%and 62%of their initial activities,respectively.Especially,PEI/PDA-M-CLEAs and N-M-CLEAs exhibited higher starch hydrolysis efficiency than freeα-amylase.The maximum dextrose equivalent(DE)values of starch hydrolysis by PEI/PDA-M-CLEAs and N-M-CLEAs reached 29.24%and 28.79%within 90 min,respectively.However,the maximum DE values of starch hydrolysis by the freeα-amylase was only 27.89%even in 150 min.The magnetic cross-linkedα-amylase aggregates could be introduced as effective biocatalyst for industrial applications in production of maltose syrups.

Starch-Based Adhesives for Wood/Wood Composite Bonding: Review

Increasing global energy crisis and scarcity of petroleum resources has shifted focus of chemical industries to look for alternative raw material resources. The main focus of raw materials in wood adhesives, such as petroleum and natural gas [1] [2], would be gradually replaced by renewable biopolymers. Starch is a relatively inexpensive and renewable product from abundant plants, easy processing and it has been extensively used as binders, sizing materials, glues and pastes [3], but its bonding capacity is not strong enough to glue wood [4]. Extensive research has been carried out on improving the cohesive properties, especially water resistance, of starch-based adhesives. In starch-based wood adhesive many new approaches have come forward for effective use it in wood/wood composite adhesive giving comparable performance as synthetic adhesives. This review of starch-based adhesives is made with the focus on starch modification methods for improving properties of starch-based adhesives.

Heterogeneous Reactions between Starch and AKD under Solvent-free Conditions

Oxidized starch powder and cationic starch solution were reacted with alkyl ketene dimer(AKD) under heterogeneous conditions at 70℃ for 12 h.The AKD molecules reacted with starch hydroxyl groups to form β-keto ester linkages under the above conditions.The reaction products were separated into CHCl_3-soluble and CHCl_3-insoluble fractions.FT-IR spectroscopy,SEM,Xray diffraction,and TG-DTA analyses of the CHCl_3-insoluble fraction indicated that β-keto ester substituents were introduced to hydroxyl groups on the starch surfaces.The results indicated that hydrogen bonds between the starch molecules were disrupted under heterogeneous conditions upon heating.The activity and accessibility of hydroxyl groups were enhanced,as a result of which β-keto ester bonds were produced between AKD and starch.Based on these results,we speculate that the β-keto esters which existed in the sheets sized by AKD emulsions were generated by the reaction between AKD and starch.

Modified-starch Consolidation of Alumina Ceramics

The alumina ceramics with the homogeneous microstructure and the higher density were fabricated via the modified-starch consolidation process by 1.0 wt% of a modified starch as a consolidator/ binder. The swelling behavior of the modified oxidized tapioca starch was analyzed by optical microscope, and two other corn starches （common corn starch and high amylose corn starch） were also analyzed for comparison. The modified starch used as a binder for the consolidation swelled at about 55 ℃, began to gelatinize at 65 ℃ and then was completely gelatinized at 75 ℃. But the corn starches could not be completely gelatinized even at 80 ℃ for 1 h. The high-strength green bodies （10.6 MPa） with the complex shapes were produced. The green bodies were sintered without any binder burnout procedure at 1 700 ℃ and a relative density of 95.3% was obtained for the sintered bodies, which is similar to that of the sintered sample formed by conventional slip casting. In addition, the effect of temperature on the apparent viscosity of the starch/alumina slurry in the process was investigated, and the corresponding mechanism for the starch consolidation was discussed.

Selective Oxidation of Aldehyde over Hydroxymethyl Group Catalyzed by Gold Nanoparticles in Aqueous Phase

A protocol for selectively oxidizing aldehyde over hydroxymethyl group is developed, using biomass starch protected gold nanoparticles (NPs) as catalyst. The Au NPs show high selectivity that aldehyde is oxidized into carboxylic acid while alcoholic hydroxyl group stays intact in selective oxidation of 4-(hydroxymethyl)-benzaldehyde. The heterogeneous catalysis system is composed of soluble catalysts and insoluble substrate. The gold catalyst is prepared, preserved and applied for catalytic oxidation all in water. After reaction conditions are optimized, H2O2 is found to be the best oxidizing agent with complete conversion.Besides, the gold catalyst displays good versitility for aldehyde derivatives. After reaction completes, organic components are extracted by organic solvent and gold NPs in water are separated and recycled.

Small molecule interfacial cross-linker for highly efficient two-dimensional perovskite solar cells

The nonradiative recombination of charge carriers at the hole transport layer(HTL)/perovskite interface generally induces remarkable performance loss of the inverted two-dimensional perovskite solar cells(2D PSCs). Herein, a cross-linkable small molecule of 2-mercaptoimidazole(2-MI) was introduced into the nickel oxide(NiO_(x))/2D perovskite interface. Experiments have confirmed the formation of Ni-N covalent bond by N atom in the 2-MI and Ni in the NiO_(x) and the coordinating between S atom of 2-MI and under-coordinated Pb^(2+) near to the NiO_(x)/perovskite interface, which contributes to creating a crosslinking between NiO_(x)/perovskite interface to restrain charge carrier recombination and enhance the extraction of hole carriers at the interface. Besides, the 2-MI modification layer is also beneficial for promoting the crystallinity of 2D perovskite. Consequently, the inverted 2D PSCs with 2-MI modification achieved the best power conversion efficiency of 15%. This paves a route to acquire highly efficient 2D PSCs by constructing a cross-linking at the NiO_(x)HTL/2D perovskite interface.

Synthesis and Excellent Antibacterial Activity of Ag_(2)O-Loaded Carboxymethyl Starch Nanocomposites

Carboxymethyl starch/silver oxide nanocomposites(CMS-Ag_(2)O NCs)were successfully fabricated by modifying carboxymethyl starch(CMS)with Ag_(2)O obtained from an aqueous AgNO_(3)solution as silver source.Ag_(2)O nanoparticles(NPs)formed on the surface of CMS by ion exchange.Based on SEM images,the diameters of Ag_(2)O NPs were determined to be between 50 and 100 nm.From the XRD spectra of CMS-Ag_(2)O NCs,the new diffraction peaks appeared at 33.88°and 38.08°,which were attributed to the Ag_(2)O NPs.According to the XPS analysis,Ag 3d_(5/2)and Ag 3d_(3/2)peaks in CMS-Ag_(2)O NCs were fitted into two main peaks centered at 367.6 eV and 373.6 eV,which were attributed to Ag^(+).The antibacterial efficiencies of CMS-Ag_(2)O NCs against Escherichia coli,Staphylococcus aureus,Pseudoalteromonas tetraodonis,Micrococcus luteus,and Shewanella putrefaciens were determined to be 99.6%,99.7%,99.4%,99.5%,and 99.6%,respectively.The antibacterial efficiencies of CMS-Ag_(2)O NCs against the bacterial species were all greater than 99%.Therefore,these results indicated that CMS-Ag_(2)O NCs was highly effective as a bactericidal agent against multiple bacterial species.CMS-Ag_(2)O NCs can be further applied to antifouling coating.

氧化淀粉交联改性聚乙烯醇表面施胶剂的制备与性能研究

采用氧化交联法制备“氧化淀粉交联改性聚乙烯醇(PVA)表面施胶剂”。结果显示,氧化淀粉交联改性聚乙烯醇表面施胶剂合成的最佳工艺条件是玉米淀粉用量是20g,H_(2)O_(2)和硼砂相对淀粉质量分数分别是6%和2.0%,熬胶时间是60min。当氧化剂用量为单一变量且其数值为6%,纸页强度性能参数抗张指数达到66.67N.m/g、耐破指数4.10kPa.m^(2)/g和环压指数10.64N.m/g,效果相对最佳,同时,施胶度30.8g/m^(2),数值最低,抗水性最好。纸页涂布氧化淀粉胶、聚乙烯醇胶和氧化淀粉交联聚乙烯醇胶后的厚度分别增加0.03mm、0.06mm和0.12mm。结论:“氧化淀粉交联聚乙烯醇胶”后纸页的厚度增加最多,说明氧化淀粉与聚乙烯醇交联改性后的纸页表面施胶剂能有效地防止聚乙烯醇向原纸内的渗透,能进一步强化其提高纸页抗水性和纸页强度等方面的性能。

氧化玉米淀粉/明胶复合胶囊壳的制备与表征

目的:采用改性淀粉与明胶共混制备胶囊壳,降低胶囊壳制备成本。方法:以玉米原淀粉为原料,采用15%用量的过氧化氢氧化制备氧化玉米淀粉,与明胶共混,分别通过流延法和浸渍法制备了氧化玉米淀粉/明胶复合胶囊膜和胶囊壳,并采用傅里叶变换红外光谱(FT-IR)、X射线衍射(XRD)、扫描电子显微镜(SEM)对其进行表征。结果:当氧化玉米淀粉与明胶质量比为5∶5,制备的氧化玉米淀粉/明胶复合胶囊壳的干燥失重在13.0%~15.0%,在蒸馏水和模拟人工胃液中的崩解时限在10 min以内,脆碎度不超过5粒。结论:采用氧化玉米淀粉与明胶共混制备的复合胶囊壳性能符合《中国药典》(2020)要求。

蝶豆花提取物-马铃薯氧化羟丙基淀粉/果胶指示标签的制备及应用

为实现冷鲜牛肉新鲜度的无损、实时及可视化监测,以马铃薯氧化羟丙基淀粉(potato oxidized hydroxypropyl starch,POHS)和果胶(pectin,P)作为成膜基材,添加蝶豆花提取物(Clitoria ternatea extract,CT)制备智能指示标签(P/POHS/CT),并将该标签应用于冷鲜牛肉的货架期检测。结果表明,CT添加量为1.0%(体积分数)的标签性能最佳,其拉伸强度为16.62 MPa,溶胀度为367.68%,显著高于其他组(P<0.05),含水率为10.42%,水蒸气渗透率为1.32×10^(-7)g/(m·s·Pa),显著低于其他组(P<0.05),扫描电镜结构紧密,红外光谱显示各组分间相容性较好。在贮藏过程中,随着贮藏时间延长,冷鲜牛肉的pH值、挥发性盐基氮含量、硫代巴比妥酸反应物值及菌落总数均显著升高(P<0.05),贮藏第4天时为次级新鲜度,第7天时腐败,智能指示标签的色泽对应的从紫色变为蓝色、绿色。结果表明,适量CT的添加可以改善智能标签的性能,且该标签对冷鲜牛肉新鲜度的变化响应能力强,具有作为预测冷鲜牛肉新鲜度变化的智能包装材料的潜质。

烟用接装纸原纸非挥发性物质总迁移量影响因素分析

针对各卷烟材料厂提出烟用接装纸原纸中非挥发性物质总迁移量的要求,比对分析四台纸机生产的烟用接装纸原纸中非挥发性物质总迁移量以及生产工艺的差异,结果表明:表面施胶对其影响最大,不进行表面施胶时非挥发性物质总迁移量值最低,使用表面施胶时,CMC对其影响要高于氧化淀粉,针对不同客户要求,要设定不同的施胶量标准,以保证能够完全满足客户要求,提高产品市场竞争力。