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    25 June 2020, Volume 40 Issue 3 Previous Issue    Next Issue
    Research Progress in Biosynthesis of Anthocyanins
    Qian XU,Chen ZHANG,Jiawei WU,Jia OUYANG
    2020, 40 (3):  1-11.  doi: 10.3969/j.issn.0253-2417.2020.03.001
    Abstract ( 2670 )   HTML ( 1967701126 )   PDF (3662KB) ( 1474 )   Save

    Anthocyanin is a kind of flavonoid which mainly exists in plants. It has strong biological activities such as anti-cancer and anti-oxidation, and is widely used in the field of nutrition and health care. Most anthocyanins are extracted directly from plants by physical or chemical means, but the yield is low, and the extracted anthocyanins are mostly mixtures due to the restrictions of time, region and season. Biosynthesis of anthocyanins have attracted much attention by researchers worldwide in recent years. As the biosynthesis of anthocyanins can be controlled artificially and the purity of the obtained products is high, it has been widely studied. Anthocyanins cannot exist stably in the environment, and need to be modified by glycosylation, acylation and methylation to increase their stability. The modified anthocyanins can be synthesized by microorganisms and significant color changes can be seen in the medium. The biosynthesis and modification of anthocyanins were reviewed in this paper, and the preparation technology of anthocyanin synthesis from plants and microorganisms was briefly introduced, the factors affecting anthocyanin synthesis were analyzed, and finally the future research direction of anthocyanin was predicted.

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    A Review of Deep Eutectic Solvents for Lignin Isolation
    Lei ZHONG,Chao WANG,Gaojin LYU,Xingxiang JI,Guihua YANG,Jiachuan CHEN
    2020, 40 (3):  12-22.  doi: 10.3969/j.issn.0253-2417.2020.03.002
    Abstract ( 1869 )   HTML ( 1193765908 )   PDF (1494KB) ( 1464 )   Save

    Lignin is the most abundant renewable aromatic polymer in nature, which complex structure and compact connection with cellulose and hemicellulose through covalent bond and hydrogen bond make it difficult to be separated efficiently. Deep eutectic solvents (DES) is a novel kind of green ionic liquid, which has been successfully applied to lignin isolation due to its unique physical and chemical properties. The research progress of dissolution and extraction of lignin by deep eutectic solvents (DES) is reviewed in detail. From the point of view of the mechanism of dissolving lignin by DES, the effects of different factors(composition, proportion, pH value, functional groups of DES, water content of system, raw material, reaction time, temperature, catalyst, co-solvent, and so on) on lignin removal were emphatically expounded. Based on the research progress of DES in lignin extraction, the research progress and futuer application of lignin extraction were summarized and prospected.

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    Preparation and Properties of Cellulose-based Integrated Sandwich Structure Supercapacitor
    Yumeng HU,Minjie HOU,Miaojun XU,Bin LI
    2020, 40 (3):  23-30.  doi: 10.3969/j.issn.0253-2417.2020.03.003
    Abstract ( 782 )   HTML ( 1377870869 )   PDF (14583KB) ( 594 )   Save

    A cellulose-based highly conductive film (RGO/CNF/RGO(RCR)) was prepared using graphene oxide (GO) and cellulose nanofiber (CNF). Graphene oxide@polypyrrole (GO@PPy) active material was deposited on both sides of the film, then an integrated flexible film with conductive anisotropy and good flexibility was acquired. Furthermore, the liquid electrolyte was infiltrated into the composite film, and the copper foil was used as the current collector to prepare the integrated sandwich structure supercapacitor(SC). The morphology and surface elements of the film were analyzed by scanning electronic microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Afterwards, the electrochemical performance of integrated capacitor was compared with stacked capacitor and gel capacitor. The results showed that PPy was wrapped on the surface of GO and deposited on the surface of RCR film in the form of GO@PPy, and a pseudo-capacitive layer of about 400 nm was formed. When the scanning rate was 5 mV/s, the area specific capacitances of integrated, stacked and gel capacitor reached the maximum, which were 28.5, 28.1 and 33.8 mF/cm2, respectively. When the scanning rate increased to 200 mV/s, the area specific capacitances decreased to 4.6, 3.2 and 1.1 mF/cm2, respectively. It could be seen that the integrated capacitor has higher stability. The tight and seamless connection of the integrated capacitor could effectively avoid the relative displacement and shedding between the adjacent components, and effectively reduce the resistance of electron/ion transfer. At the same time, the integrated capacitor also showed better flexibility, and its electrical performance remained stable after bending test. When the current density was 0.2 mA/cm2, the area and volume specific capacitance of the integrated capacitor could reach 64.8 mF/cm2 and 31.0 F/cm3, respectively, showing excellent electrochemical performance. The preparation of the integrated supercapacitor provides a new method for development of wearable electronic devices.

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    Analysis of Monosaccharide in Sesbania cannabina Seed Enzymatic Hydrolysate by Pre-column Derivatization Reversed-phase High Performance Liquid Chromatography
    Qiannan ZHANG,Fangmin XU,Zhina LIAN,Xin LI,Qiang YONG
    2020, 40 (3):  31-38.  doi: 10.3969/j.issn.0253-2417.2020.03.004
    Abstract ( 428 )   HTML ( 5 )   PDF (775KB) ( 513 )   Save

    To establish a pre-column derivatization reversed-phase high performance liquid chromatography for the determination of mannose, glucose, galactose and xylose in the enzymatic hydrolysate of Sesbania cannabina seed, the pre-column derivatization was carried out by using 1-phenyl-3-methyl-5-pyrazolone (PMP) as derivatization reagent, and the effects of different chromatographic conditions were investigated. The experimental results showed that when the mobile phase was acetonitrile/potassium dihydrogen phosphate buffer solution (0.02 mol/L, pH value 6.5) and the derivatization conditions were PMP dosage 150 μL, reaction time 80 min, reaction temperature 60℃ and chloroform extraction for 3 times, the peak area of each monosaccharide component was larger and the separation effect was better. The methodological study verified that the R2 values of standard curves of four monosaccharide were over 0.999 4, the recovery rates were 96.9%-104.8%, the RSD values were lower than 0.56%, and the results repeatability, stability and precision tests were good, which indicated that the established method under these conditions was effective and convincible. The mass ratio of mannose, glucose, galactose and xylose was 1:0.44:1.92:0.53. In summary, pre-column derivatization high performance liquid chromatography provided a quantitative method with simple operation, accuracy, high resolution and good reproducibility for analyzing monosaccharide composition and content of the enzymatic hydrolysate of S. cannabina seed.

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    Effect of Pore Structure on HCN Defence Performance of Activatied Carbon Supported Metallic Oxide Catalyst
    Hao SUN,Dali ZHAO,Yanren JIN,Yanyan LIU,Jianchun JIANG,Haoyang XING
    2020, 40 (3):  39-44.  doi: 10.3969/j.issn.0253-2417.2020.03.005
    Abstract ( 493 )   HTML ( 39 )   PDF (3372KB) ( 554 )   Save

    A series of coal activated carbon supported metallic oxide were preparedby incipient-wetness impregnation method with cuprammonium complex and so on.The pore structure, metal distribution and morphology of activated carbon before and after loading of metal sites were analyzed by N2 adsorption-desorption, scanning electron microscope, energy dispersive spectroscopy and transmission electron microscope.The HCN defence time of carbon catalyst was also tested. Hence, the effect of pore size distribution of activated carbon supportor on the HCN defence performance of catalyst was demonstrated.The effective pore size distribution of activated carbon for adsorbing cuprammonium complex was 1.2-2.1 nm, which facilitated the penetration of cuprammonium complex inside the carbon supportor and formation of the active sites for dispersing Cu2O and enhancement of HCN defence time. However, the mesopores(>2.1 nm) of carbon supportor would result in the severe accumulation of the active particles, reduction of metal dispersion and thus decreasing the HCN defence performance of carbon catalysts.The HCN defence time of activated carbon supported catalyst was longer than 30 min, as the pore volume of activated carbon with the pore size of 1.2-2.1 nm was over 0.142 4 cm3/g and the pore volume with the pore size of >2.1 nm was less than 0.082 4 cm3/g.

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    Preparation and Compression-resilience Property of Soybean Protein/Polyacrylamide Composite Hydrogels
    Jingya NAN,Gaitong ZHANG,Lijun WANG,Fuxiang CHU,Chunpeng WANG
    2020, 40 (3):  45-51.  doi: 10.3969/j.issn.0253-2417.2020.03.006
    Abstract ( 754 )   HTML ( 10547201 )   PDF (3693KB) ( 729 )   Save

    A novel soybean protein/polyacrylamide (SPI/PAAm) composite hydrogel was synthesized, in which soybean protein (SPI) and acrylamide (AAm) were used as raw materials, ammonium persulfate (APS) was used as the initiator, N, N'-methylenebisacrylamide (MBAA) was used as the covalent crosslinker, CaCl2 was used as the ionic crosslinker and N, N, N', N'-tetramethylethylenediamine (TEMED) was used as the accelerator. The structure and mechanical properties of the obtained hydrogels were analyzed, and the mechanical mechanism was then investigated. The results suggest that the obtained hydrogel had a double-network structure, including ionically-crosslinked soybean protein network and covalently-crosslinked polyacrylamide network. For the double-network hydrogel, the ionically-crosslinked network dispersed the applied stress and dissipated the energy, and the covalently-crosslinked network contributed to the shape retention. The synergistic effect resulting fromdouble networks endowed the hydrogel with high elasticity, high compressibility and fatigue resistance.The morphology analysis revealed that the obtained hydrogel showed a uniform cell structure, and the soybean protein was uniformly distributed within the hydrogel. The mechanical analysis indicated that the obtained hydrogel exhibited high compression-resilience property and elasticity, which could rapidly recover to its original shape upon 80% compressive strain without structural collapse or damage during 10 successive uniaxial compression cycles. More encouragingly, the obtained hydrogel possessed outstanding toughness and fatigue resistance, which could remain shape intact after undergoing 100 compression cycles at 20%, 50% and 80% strain, respectively.After 100 compression cycles at 20%, 50% and 80% strain, the corresponding stress remaining rates were 90%, 95% and 104%, the corresponding plastic deformation rates were 3.1%, 5.9%and 8.4%, and all the energy loss coefficients were below 0.3.

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    Preparation and Characterization of Lignocellulosic Aerogel with High Liquid Absorbability
    Jinxiu WU,Yong DONG,Jianyu XIA,Yan CHEN,Yunfeng CAO,Zhulan LIU
    2020, 40 (3):  52-60.  doi: 10.3969/j.issn.0253-2417.2020.03.007
    Abstract ( 481 )   HTML ( 5 )   PDF (3899KB) ( 557 )   Save

    Ethylenediamine (EDA) pretreated soybean pretreated with ethylenediamine (EDA) stem was dissolved in LiCl/DMSO with different mass fractions (1%, 2%, 3% and 4%), then was gelated in ethanol and freeze-dried to prepare lignocellulose aerogels (SBS-AG-1-SBS-AG-4) with high liquid absorption capacity, and the microstructure, porosity and absorption of these aerogels were tested and characterized in detail. The results showed that if the lignocellulose was dissolved with relatively higher mass fraction (4%), the aerogel could be fabricated with larger specific surface area and better mechanical strength, but formed the denser fiber interwoven network structure, smaller aperture and lower absorbability, its specific surface area, compression strength and energy storage modulus were 198.52 m2/g, 135.56 kPa(50%strain) and 798.91 kPa(shear stress 100 Pa), and the adsorption rates for water, diesel and silicone oil within 30s were 8.45, 5.77 and 6.39 g/g, respectively. While, for the obtained aerogels obtained with containing lower lignocellulose mass fraction (1%), their looser internal network structure and larger pore size could help to improve liquid absorption capacity, Moreover, SBS-AG-1 could achieve equilibrium adsorption of water, diesel and silicone oil within 30 s, and its their adsorption rates were as high as 22.63, 18.57 and 21.53 g/g.

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    Synchronous Synthesis of Carbon Nanodots Formed on Pre-hydrolysis of Lignocellulose
    Shunli LI,Yu LIU,Fei HUANG,Kai LIU,Honglei CHEN
    2020, 40 (3):  61-68.  doi: 10.3969/j.issn.0253-2417.2020.03.008
    Abstract ( 419 )   HTML ( 13 )   PDF (3537KB) ( 571 )   Save

    During the process of hot water pre-hydrolysis of eucalyptus wood chips, a tiny amounts of urea was added to obtain the hot water pre-hydrolysis liquor.The produced pre-hydrolysis liquor(PHL) showed excellent fluorescence with the properties of concentration quenching and excitation wavelength dependence. The existence of graphite carbon structure in the pre-hydrolysis liquor was confirmed by X-ray diffraction (XRD) and Raman spectroscopy. The analysis of transmission electron microscopy (TEM) and atomic force microscopy (AFM) confirmed that graphite carbon existed in the form of carbon nanodots (CNDs) and the quantum yield was 19.43%. Furthermore, the structure and composition of CNDs were characterized by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR). The results showed that the surface of CNDs was rich in functional groups such as hydroxyl, carboxyl and amino groups, CNDs were successfully doped with N element, and the fluorescence intensity of CNDs was relatively stable when the pH value was 3.67-9.42.The average life of CNDs was 3.07 ns.

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    Synthesis of Aluminum Phosphate with Dehydroabietylamine as Structure Directing Agent
    Chen YANG,Guihua ZHU,Yaming WANG,Zhihua LIU,Lihong JIANG,Pei HE
    2020, 40 (3):  69-75.  doi: 10.3969/j.issn.0253-2417.2020.03.009
    Abstract ( 440 )   HTML ( 9 )   PDF (1908KB) ( 517 )   Save

    Aluminum phosphate was synthesized through microwave-assisted solvothermal method with dehydroabietylamine as the structure directing agent and pinene as the solvent. The products were characterized by X-ray diffraction, nitrogen adsorption-desorption, scanning electron microscope, transmission electron microscope, thermal gravimetric analysis and temperature-programmed infrared. The results indicated that the reaction temperature and duration showed significant effect on the phase and porosity of the aluminum phosphate, and the product with good porosity was obtained under the conditions of temperature 170℃ and duration 4 h or more. The typical sample possessed "sticky" morphology with amorphous structure, and micro- and meso-porous with the BET specific surface area of 272.00 m2/g, average pore size of 3.01 nm and huge pore volume of 0.69 cm3/g. The results also confirmed the existence of dehydroabietylamine in the as-synthesized aluminum phosphate, which confirmed the structure-directing property of the dehydroabietylamine.

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    Synthesis and Herbicidal Activity of Citral-based Thiosemicarbazone Compounds
    Yun HE,Wengui DUAN,Guishan LIN,Bo CEN,Junwen BU,Fuhou LEI
    2020, 40 (3):  76-84.  doi: 10.3969/j.issn.0253-2417.2020.03.010
    Abstract ( 557 )   HTML ( 15 )   PDF (923KB) ( 566 )   Save

    Twenty-six novel citral-based thiosemicarbazone compounds 2a-2m (thirteen pairs of (2Z, 1E)/(2E, 1E)-isomers) were designed and synthesized in an attempt to develop potent herbicidal agents. The structures of the target compounds were characterized by FT-IR, NMR, and ESI-MS. The herbicidal activities of the target compounds were preliminarily evaluated in vitro against Brassica campestris and Echinochloa crusgalli. The bioassay results indicated that compounds (2Z, 1E)-2a (R=Me), (2E, 1E)-2a (R=Me), (2Z, 1E)-2b (R=Et), (2E, 1E)-2b (R=Et), and (2E, 1E)-2c (R=i-Pr) displayed inhibition rates of 82.6%, 88.7%, 80.2%, 80.5% and 82.0%, respectively, against the root-growth of rape (Brassica campestris) at the concentration of 100 mg/L. They were much better herbicidal activity than the commercial herbicide flumioxazin. It was found that the herbicidal activity of the compounds with aliphatic groups (R) was much better than that of the compounds with aromatic groups (R), and the (2E, 1E)-isomers bearing aliphatic groups (R) exhibited better inhibition activity than corresponding (2Z, 1E)-isomers, whereas the (2Z, 1E)-isomers bearing aromatic groups (R) showed better inhibition activity than their (2E, 1E)-isomers. The electrostatic potential and the frontier molecular orbitals of the best activity compound (2E, 1E)-2a were calculated and analyzed. This implied that the thiourea moiety was critical for the bioactive performance and the small R group was favorable for bioactivity.

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    Chemical Component and Inhibition Activity Against Candida albicans of Sapindus mukorossi Peel Extract
    Jindan QIU,Lu LI,Minping WEI,Yunfei XIE,Hang YU,Weirong YAO
    2020, 40 (3):  85-91.  doi: 10.3969/j.issn.0253-2417.2020.03.011
    Abstract ( 630 )   HTML ( 2085 )   PDF (2705KB) ( 716 )   Save

    The pericarp of Sapindus mukorossi was extracted by water fermentation extract and ethanol extract and two kinds of extracts were obtained, with the comparative analysis of the chemical composition of two methods.The results showed that the purity of total saponins in water fermentation extract(WFE) (80.23%) was higher than that of ethanol extract(EE)(75.50%). Based on HPLC-DAD/MS, a total of 13 saponins were identified including 6 kinds of sesquiterpene glycosides and 7 kinds of triterpenoid saponins.WFE and EE both contained 12 saponins, of which triterpenoid saponins accounted for 66.07% and 80.39%, respectively. The MIC and MBC were used to compare in vitro antifungal activities. It was found that the WFE and EE all had significant antifungal activities, the MIC values were 62.50 and 31.25 mg/L and the MBC values were 250 and 125 mg/L, respectively. A mouse model of vulvovaginal candidiasis(VVC)was established to examine in vivo inhibitory effects. Compared with the negative group, the WFE significantly reduced (P < 0.05) the fungal burden and inflammatory factor (IL-6, IL-8). Both WFE and EE could improve VVC histopathology (P < 0.05). Therefore, S.mukorossi pericarp extracts had antifungal activity against Candida albicans in vitro and in vivo, and the treatment effect of the WFE was better.

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    Preparation and Properties of Non-ionic Self-emulsified Waterborne Epoxy Curing Agents Derived from Tung Oil
    Xiaohua YANG,Haiyang DING,Shouhai LI,Lina XU,Yamei LIN,Mei LI
    2020, 40 (3):  92-98.  doi: 10.3969/j.issn.0253-2417.2020.03.012
    Abstract ( 578 )   HTML ( 14 )   PDF (1124KB) ( 719 )   Save

    The adduct of eleostearic acid methyl ester and maleic anhydride(TMA), was carried out the amidation reaction with triethylenetetra mine were performed to achieve polyamide curing agent derived from tung oil (TMAPA). Then, ring-opening addition of TMAPA with polyethylene glycol diglycidyl ether, followed by termination reaction between paraformaldehyde and primary amine, by which non-ionic waterborne epoxy curing agents derived from tung oil(TMAWCA) was obtained. The chemical structure of the intermediates and the targeted products were confirmed by Fourier transform infrared spectroscopy (FT-IR) and proton nuclear magnetic resonance (1H NMR). The result showed that the targeted products could emulsify hydrophobic liquid epoxy resin. It was found that the overall properties were best when the mass ratio of hydrophobic bisphenol F epoxy resin NPEF-170 and TMAWCA was 1.5:2 and the curing temperature was 25℃/4 h+60℃/4 h+80℃/2 h. The properties of the two-component film of NPEF-170/TMAWCA were as follows:adhesion level 1, flexibility 1 mm, pencil hardness H, impact resistance 50 kg/cm, water resistance>7 d, and water contact angle 85°.

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    In vitro Metabolism Process of Oxidative Degradation Products from Gleditsia microphylla Galactomannan
    Xinchun WANG,Wei XU,Jianxin JIANG,Liwei ZHU
    2020, 40 (3):  99-107.  doi: 10.3969/j.issn.0253-2417.2020.03.013
    Abstract ( 449 )   HTML ( 148 )   PDF (678KB) ( 581 )   Save

    The 0.3%, 0.6%, 1.5%, 3.0% and 4.5% H2O2 solutions were used to pretreat the Gleditsia microphylla galactomannan (GMG). The obtained products (GMG-0.3, GMG-0.6, GMG-1.5, GMG-3.0 and GMG-4.5) were used to simulate the metabolism of distal cecum and investigate the in vitro metabolism of GMG by intestinal microflora of SD rats. The results showed that after pretreatment with different mass fractions of H2O2, the relative molecular weights of GMG were significantly different. The molecular weight decreased from 1 039 400 to 32 060 after treatment with 4.5% H2O2; and the infrared spectroscopy analysis found that the pretreatment with H2O2 did not change the structure of GMG. By analyzing the pH value, total sugar consumption rate, reducing sugar, and short-chain fatty acid (SCFAs) and branched-chain fatty acid (BCFAs) concentrations in the metabolism broth during 48 hours, the utilization of galactomannan by the intestinal microflora was calculated. The results showed that the metabolism of the pretreated GMG experimental groups was significantly better than that of the blank control group and the non-pretreated GMG experimental group, and the metabolism of GMG-0.6 experimental group was the best. The higher concentration of acetic acid produced by metabolism was 25.36 mmoL/L, the total SCFAs concentration was 45.05 mmol/L, the consumption rate of total sugar was (52.86±3.11)%, and the mass concentration of reducing sugar first increased and then decreased to (0.002±0.003) g/L. The experimental results showed that oxidative degradation of GMG could be used as a functional food additive to decrease blood glucose, regulate insulin secretion and improve intestinal health.

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    Extraction of Dihydrofisetin from Rhus punjabensis var. sinica Rehd. Fruit by Supercritical CO2 and Its Antioxidant Activity in vitro
    Aiwen DONG,Weixin LI,Huan WANG,Yake ZOU
    2020, 40 (3):  108-114.  doi: 10.3969/j.issn.0253-2417.2020.03.014
    Abstract ( 444 )   HTML ( 19 )   PDF (572KB) ( 626 )   Save

    Rhus punjabensis var. sinica Rehd. fruit was superfinely crushed at 0-10℃ and degreased with petroleum ether (60-90℃), and then the dihydrofisetin was extracted from fruit powder by supercritical CO2 extraction. The suitable entrainer was chosen, and the extraction conditions were optimized by orthogonal experiment. The total antioxidant capacity of the obtained dihydrofisetin and its scavenging effects on DPPH·, superoxide anion radicals (O2-·) and hydroxyl radicals (·OH) were investigated. The results showed that the particle size of R. punjabensis var. sinica fruit powder could be up to 0.1-1 μm after ultrafine-pulverization and cell-wall breaking ratio was over 95%; the suitable entrainer was ethanol with volume fraction of 70%, the optimal conditions for the extraction were solid-liquid ratio 5:3(g:mL), extraction pressure 30 MPa, extraction temperature 55℃, extraction time 2 h, separating axeⅠtemperature 55℃ and pressure 10 MPa, separating axeⅡtemperature 40℃ and pressure 5 MPa. Under these conditions, the yield of dihydrofisetin was 0.46%, the purity was 80.26%. The dihydrofisetin had strong antioxidant activity, and the half-clearance concentration(IC50) of DPPH·, O2-· and ·OH were 6.93, 59.63 and 9.05 mg/L, respectively. The radical scavenging abilities on DPPH· and O2-· were close to those of VC. The scavenging capacity of ·OH and total antioxidant capacity were better than those of VC.

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    Optimization of Design of Lignin-based Activated Carbon Based on Response Surface Methodology
    Xinglong HOU,Qi GUO,Xiaopeng JIAN,Dichao WU,Wei XU,Junli LIU
    2020, 40 (3):  115-122.  doi: 10.3969/j.issn.0253-2417.2020.03.015
    Abstract ( 601 )   HTML ( 1580 )   PDF (667KB) ( 680 )   Save

    Lignin-based activated carbon was prepared from corn cob lignin by using phosphoric acid activation method.Taking methylene blue adsorption value (MB) as the index, the interaction during the preparation of activated carbon were explored by Plackett-Burman design, the steepest climbing test, and the center composite design method.The results showed that the three most important factors obtained by Plackett-Burman design were immersion ratio, activation temperature, and activation time.The best center region was determined through the steepest climbing test.The optimal process conditions obtained by the center composite design (CCD) and response surface analysis (RSM) were impregnation ratio 3:1(g:g), activation temperature 563℃, and activation time 2.75 h. The verification experiment was performed under the above optimized process of 60% phosphoric acid mass fraction, 12 h immersion time, 90℃ immersion temperature. The pore size of the lignin-based activated carbon was mainly concentrated at 2-10 nm, the BET specific surface area was 1 436 m2/g, total pore volume was 1.041 cm3/g, the micropore pore volume was 0.385 6 cm3/g and the methylene blue adsorption value (MB)was 240 mg/g.

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    Synthesis of 1, 2, 4-Thiadiazole-3, 5-dione Derivatives of Trimethoxy GallicAcid and Its Inhibition of HL60 Cell Line Proliferation
    Zhiwen QI,Hao ZHOU,Xingying XUE,Yangyang YAN,Chengzhang WANG
    2020, 40 (3):  123-129.  doi: 10.3969/j.issn.0253-2417.2020.03.016
    Abstract ( 346 )   HTML ( 6 )   PDF (635KB) ( 507 )   Save

    A series of 1, 2, 4-thiadiazole-3, 5-dione derivatives of trimethoxy gallic acid (4a-4e) were synthesized, and the intermediate products 2, 3 and the target compounds 4a-4e were tested against the proliferation of acute leukemia HL60 by MTT method.The inhibition of cell proliferation, and the synergistic effects of 4b and 4c and the positive control TDZD-8 on the proliferation inhibition of HL60 cells were investigated. The results showed that compounds 2-4 had a certain inhibitory effect on the proliferation of HL60 cells. Among them, compounds 4b and 4c had better inhibitory effects, and their half inhibitory concentrations (IC50) were 10.60 and 6.31 μmol/L, respectively and the IC50 value of TDZD-8 on HL60 cells was 0.30 mmol/L. In addition, 4b and 4c cooperated with TDZD-8 had better proliferation inhibitory effect on the acute leukemia cell line HL60. When the concentrations of 4b and TDZD-8 were 5.0 and 0.34 μmol/L, the synergistic inhibition rate of them was 94.45%, and the collaborative index(CI) value of the synergy index was 0.58; when the concentrations of 5c and TDZD-8 were 5.0 and 0.34 μmol/L, the synergistic inhibition rate was 98.76% and the CI value was 0.31. It could be seen that the new gallic acid 1, 2, 4-thiadiazole-3, 5-dione derivative could potentially act as the drug leader for treating human acute leukemia.

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    Preparation of Self-bonding Granular Activated Carbon by Alkali/Urea Dissolution System
    Xuan YANG,Chenlu HE,Yongzhi XIONG,Guanfeng LIN,Yandan CHEN,Biao HUANG
    2020, 40 (3):  130-134.  doi: 10.3969/j.issn.0253-2417.2020.03.017
    Abstract ( 517 )   HTML ( 132 )   PDF (438KB) ( 568 )   Save

    Based on the dissolution mechanism of cellulose macromolecules in alkali/urea system, self-bonding granular activated carbon was prepared with Chinese fir as raw material. The effects of different activation temperature, alkali/urea ratio and freezing conditions on the abrasion resistance and adsorption performance of granular activated carbon were discussed. The results showed that as the activation temperature increased the abrasion resistance and adsorption performance of activated carbon increased. Under the combination effect of alkali and urea, freezing process was beneficial to promote the development of activated carbon pore structure and improve the adsorption performance. Under the optimal conditions of the activation temperature 900℃, the alkali/urea mass ratio 14:36 and freezing time for 12 h, the abrasion resistance, iodine adsorption value, methylene blue adsorption value, specific surface area, total pore volume and average pore diameter of granular activated carbon were 99.12%, 1 204 mg/g, 232 mg/g, 1 365 m2/g, 0.86 cm3/g, and 2.46 nm.

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