The repairing effect of poly(N-vinylpyrrolidone-co-methacrylic acid)on permed or bleached damaged hair was studied.The combing and tensile strength of permed and bleached hair before and after treatment with the copol...The repairing effect of poly(N-vinylpyrrolidone-co-methacrylic acid)on permed or bleached damaged hair was studied.The combing and tensile strength of permed and bleached hair before and after treatment with the copolymer solution were tested,and the effects of the mass fraction of copolymer solution and immerseing time on the combing and tensile strength for permed or bleached damaged hair were investigated.The repair mechanism of permed or bleached damaged hair was also explored.The results show that when the immersing time is 3 hours,the tensile strength of the permed hair increases with the mass fraction of the copolymer solution Tensile strength within 0%-0.3%,but no obvious change is observed when250 Yield strength the mass fraction is over 0.3%.Therefore,the optimal mass 200 fraction of the copolymer solution for repairing the permed hair(cN/dtex)is 0.3%.Similarly,the optimal mass fraction of the copolymer 150strength/solution for repairing the bleached hair is 0.5%.Furthermore,the effects of immersing time on the tensile strength of the100Tensile damaged hair fibers were compared between the permed and90 bleached hair before and after treatment with the copolymer500.40.30.500.10.2 solution.Coincidentally,the optimal immersion time for permedw(P(NVP-co-MAA))/%or bleached damaged hair is both 2 hours.The tensile strength of the permed and bleached hair soaked in 0.3%and 0.5%copolymer solutions for 2 hours increases by 15.55%and 18.12%,respectively,compared to untreated hair.Through infrared spectroscopy analysis,it is found that the amide II band in hair fibers shifted to the blue after repair,with the wave number shift of 11.12 and 11.09 cm^(-1),which confirm the formation of hydrogen bonds in the hair samples.Additionally,the urea hydrogen bond disruption experiment demonstrates that urea does not disrupt the hydrogen bonds in untreated hair fibers,but prevents the formation of new hydrogen bonds in damaged hair fibers.It further validates that the improvement of the tensile strength of the copolymer treated damaged hair fibers is mainly due to the formation of hydrogen bonds.After treatment with the copolymer,the dry and wet combing friction decrease by 30.73%and 28.55%for the permed hair,and decrease by 28.55%and 24.83%for the bleached hairs,respectively.The scanning electron microscope shows that the copolymer can flatten the cuticle and fill the space between the raised cuticles.展开更多
Terephthalic acid(PTA) is practically one of the main materials of polyester. Its corresponding solid-liquid equilibrium data will provide essential support for industry design and further theoretical studies. In this...Terephthalic acid(PTA) is practically one of the main materials of polyester. Its corresponding solid-liquid equilibrium data will provide essential support for industry design and further theoretical studies. In this work,solid-liquid equilibriums of terephthalic acid in four solvents, N,N-dimethylformamide, N,N-dimethylacetamide,dimethylsulphoxide and N-methyl-2-ketopyrrolidene, were determined in the temperature range from 293.15 K to 364.6 K by dynamic method. All these data were regressed by λh model, Wilson model and NRTL model, average absolute relative deviations of which are 1.25%, 15.02% and 7.22% respectively. It indicates that λh model is mostsuitable for description of the solid-liquid equilibrium containing PTA.展开更多
Highly efficient asymmetric transcyanation of acetyltrimethylsilane with acetone cyanohydrin in an aqueous/organic biphasic system catalyzed with （R）-oxynitrilase from defatted Prunus Japonica seed meal for the prep...Highly efficient asymmetric transcyanation of acetyltrimethylsilane with acetone cyanohydrin in an aqueous/organic biphasic system catalyzed with （R）-oxynitrilase from defatted Prunus Japonica seed meal for the preparation of optically active （R）-2-trimethylsilyl-2-hydroxyl-propionitrile was successfully carried out for the first time. For better understanding of the reaction, various influential variables were examined with respect to the initial reaction rate, the substrate conversion and the product enantiomeric excess （e.e.）. Diisopropyl ether was found to be the best organic phase for this reaction among all the organic solvents tested. The optimal concentrations of Prunus Japonica seed meal powder, acetyltrimethylsilane and acetone cyanohydrin, volume ratio of aqueous phase to organic phase, buffer pH value and the reaction temperature were 34.5g·L^-1 and 14mmol· L^-1, 28mmol· L^-1, 13% （by volume）, 5.0 and 30℃, respectively, while the initial reaction rate, the substrate conversion and the product enantiomeric excess were 1.34 mmol·L^-1·h^-1, 99.0% and 99.0%, respectively. The comparative study demonstrated that silicon atom in substrate showed great effect on the reaction and acetyltrimethylsilane was a much better substrate for （R）-hydroxynitrile lyase from Prunus Japonica seed than its carbon analogue 3,3-dimethyl-2-butanone.展开更多
Improvement of coking properties of sub-bituminous coal （A） and bituminous coal （B） was done using blended organic solvents, namely, n-methyl-2-pyrrolidinone （NMP） and ethylenediamine （EDA）. Various solvent bl...Improvement of coking properties of sub-bituminous coal （A） and bituminous coal （B） was done using blended organic solvents, namely, n-methyl-2-pyrrolidinone （NMP） and ethylenediamine （EDA）. Various solvent blends were employed for the coal extraction under the total reflux condition. A low-cost ceramic membrane was fabricated using industrial waste iron ore slime of M/s TATA steel R＆D, Jamshedpur （India） to separate out the dissolved coking fraction from the solvent-coal mixture. Membrane separations were carried out in a batch cell, and around 75 % recovered NMP was reused. The fractionated coal properties were determined using proximate and ultimate analyses. In the case of bituminous coal, the ash and sulfur contents were decreased by 99.3 % and 79.2 %, respectively, whereas, the carbon content was increased by 23.9 % in the separated coal fraction. Three different cleaning agents, namely deionized water, sodium dodecyl sulphate and NMP were used to regain the original membrane permeability for the reusing.展开更多
文摘The repairing effect of poly(N-vinylpyrrolidone-co-methacrylic acid)on permed or bleached damaged hair was studied.The combing and tensile strength of permed and bleached hair before and after treatment with the copolymer solution were tested,and the effects of the mass fraction of copolymer solution and immerseing time on the combing and tensile strength for permed or bleached damaged hair were investigated.The repair mechanism of permed or bleached damaged hair was also explored.The results show that when the immersing time is 3 hours,the tensile strength of the permed hair increases with the mass fraction of the copolymer solution Tensile strength within 0%-0.3%,but no obvious change is observed when250 Yield strength the mass fraction is over 0.3%.Therefore,the optimal mass 200 fraction of the copolymer solution for repairing the permed hair(cN/dtex)is 0.3%.Similarly,the optimal mass fraction of the copolymer 150strength/solution for repairing the bleached hair is 0.5%.Furthermore,the effects of immersing time on the tensile strength of the100Tensile damaged hair fibers were compared between the permed and90 bleached hair before and after treatment with the copolymer500.40.30.500.10.2 solution.Coincidentally,the optimal immersion time for permedw(P(NVP-co-MAA))/%or bleached damaged hair is both 2 hours.The tensile strength of the permed and bleached hair soaked in 0.3%and 0.5%copolymer solutions for 2 hours increases by 15.55%and 18.12%,respectively,compared to untreated hair.Through infrared spectroscopy analysis,it is found that the amide II band in hair fibers shifted to the blue after repair,with the wave number shift of 11.12 and 11.09 cm^(-1),which confirm the formation of hydrogen bonds in the hair samples.Additionally,the urea hydrogen bond disruption experiment demonstrates that urea does not disrupt the hydrogen bonds in untreated hair fibers,but prevents the formation of new hydrogen bonds in damaged hair fibers.It further validates that the improvement of the tensile strength of the copolymer treated damaged hair fibers is mainly due to the formation of hydrogen bonds.After treatment with the copolymer,the dry and wet combing friction decrease by 30.73%and 28.55%for the permed hair,and decrease by 28.55%and 24.83%for the bleached hairs,respectively.The scanning electron microscope shows that the copolymer can flatten the cuticle and fill the space between the raised cuticles.
基金Supported by China Petroleum & Chemical Corporation(No.200049).
文摘Terephthalic acid(PTA) is practically one of the main materials of polyester. Its corresponding solid-liquid equilibrium data will provide essential support for industry design and further theoretical studies. In this work,solid-liquid equilibriums of terephthalic acid in four solvents, N,N-dimethylformamide, N,N-dimethylacetamide,dimethylsulphoxide and N-methyl-2-ketopyrrolidene, were determined in the temperature range from 293.15 K to 364.6 K by dynamic method. All these data were regressed by λh model, Wilson model and NRTL model, average absolute relative deviations of which are 1.25%, 15.02% and 7.22% respectively. It indicates that λh model is mostsuitable for description of the solid-liquid equilibrium containing PTA.
文摘Highly efficient asymmetric transcyanation of acetyltrimethylsilane with acetone cyanohydrin in an aqueous/organic biphasic system catalyzed with （R）-oxynitrilase from defatted Prunus Japonica seed meal for the preparation of optically active （R）-2-trimethylsilyl-2-hydroxyl-propionitrile was successfully carried out for the first time. For better understanding of the reaction, various influential variables were examined with respect to the initial reaction rate, the substrate conversion and the product enantiomeric excess （e.e.）. Diisopropyl ether was found to be the best organic phase for this reaction among all the organic solvents tested. The optimal concentrations of Prunus Japonica seed meal powder, acetyltrimethylsilane and acetone cyanohydrin, volume ratio of aqueous phase to organic phase, buffer pH value and the reaction temperature were 34.5g·L^-1 and 14mmol· L^-1, 28mmol· L^-1, 13% （by volume）, 5.0 and 30℃, respectively, while the initial reaction rate, the substrate conversion and the product enantiomeric excess were 1.34 mmol·L^-1·h^-1, 99.0% and 99.0%, respectively. The comparative study demonstrated that silicon atom in substrate showed great effect on the reaction and acetyltrimethylsilane was a much better substrate for （R）-hydroxynitrile lyase from Prunus Japonica seed than its carbon analogue 3,3-dimethyl-2-butanone.
文摘Improvement of coking properties of sub-bituminous coal （A） and bituminous coal （B） was done using blended organic solvents, namely, n-methyl-2-pyrrolidinone （NMP） and ethylenediamine （EDA）. Various solvent blends were employed for the coal extraction under the total reflux condition. A low-cost ceramic membrane was fabricated using industrial waste iron ore slime of M/s TATA steel R＆D, Jamshedpur （India） to separate out the dissolved coking fraction from the solvent-coal mixture. Membrane separations were carried out in a batch cell, and around 75 % recovered NMP was reused. The fractionated coal properties were determined using proximate and ultimate analyses. In the case of bituminous coal, the ash and sulfur contents were decreased by 99.3 % and 79.2 %, respectively, whereas, the carbon content was increased by 23.9 % in the separated coal fraction. Three different cleaning agents, namely deionized water, sodium dodecyl sulphate and NMP were used to regain the original membrane permeability for the reusing.
