Light emitting diodes(LEDs)have accounted for most of the lighting market as the technology matures and costs continue to reduce.As a new type of e-waste,LED is a double-edged sword,as it contains not only precious an...Light emitting diodes(LEDs)have accounted for most of the lighting market as the technology matures and costs continue to reduce.As a new type of e-waste,LED is a double-edged sword,as it contains not only precious and rare metals but also organic packaging materials.In previous studies,LED recycling focused on recovering precious and strategic metals while ignoring harmful substances such as organic packaging materials.Unlike crushing and other traditional methods,hydrothermal treatment can provide an environment-friendly process for decomposing packaging materials.This work developed a closed reaction vessel,where the degradation rate of plastic polyphthalamide(PPA)was close to 100%,with nano-TiO_(2)encapsulated in plastic PPA being efficiently recovered,while metals contained in LED were also recycled efficiently.Besides,the role of water in plastic PPA degradation that has been overlooked in current studies was explored and speculated in detail in this work.Environmental impact assessment revealed that the proposed recycling route for waste LED could significantly reduce the overall environmental impact compared to the currently published processes.Especially the developed method could reduce more than half the impact of global warming.Furthermore,this research provides a theoretical basis and a promising method for recycling other plastic-packaged e-waste devices,such as integrated circuits.展开更多
Microplastics are persistent anthropogenic pollutants that have become a global concern due to their widespread distribution and unfamiliar threat to the environment and living organisms. Conventional technologies are...Microplastics are persistent anthropogenic pollutants that have become a global concern due to their widespread distribution and unfamiliar threat to the environment and living organisms. Conventional technologies are unable to fully decompose and mineralize plastic waste. Therefore, there is a need to develop an environmentally friendly, innovative and sustainable photocatalytic process that can destroy these wastes with much less energy and chemical consumption. In photocatalysis, various nanomaterials based on wide energy band gap semiconductors such as TiO2 and ZnO are used for the conversion of plastic contaminants into environmentally friendly compounds. In this work, the removal of plastic fragments by photocatalytic reactions using newly developed photocatalytic composites and the mechanism of photocatalytic degradation of microplastics are systematically investigated. In these degradation processes, sunlight or an artificial light source is used to activate the photocatalyst in the presence of oxygen.展开更多
A plastic may degrade in response to a trigger.The kinetics of degradation have long been characterized by the loss of weight and strength over time.These methods of gross characterization,however,are misleading when ...A plastic may degrade in response to a trigger.The kinetics of degradation have long been characterized by the loss of weight and strength over time.These methods of gross characterization,however,are misleading when plastic degrades heterogeneously.Here,we study heterogeneous degradation in an extreme form:the growth of a crack under the combined action of chemistry and mechanics.An applied load opens the crack,exposes the crack front to chemical attack,and causes the crack to outrun gross degradation.We studied the crack growth in polylactic acid(PLA),a polyester in which ester bonds break by hydrolysis.We cut a crack in a PLA film using scissors,tore it using an apparatus,and recorded the crack growth using a camera through a microscope.In our testing range,the crack velocity was insensitive to load but was sensitive to humidity and pH.These findings will aid the development of degradable plastics for healthcare and sustainability.展开更多
[Objective] This study aimed to solve the mulch plastic film pollution problems in Xinjiang, in order to provide reliable theoretical basis for the research on the degradation mechanism of biodegradable plastic films....[Objective] This study aimed to solve the mulch plastic film pollution problems in Xinjiang, in order to provide reliable theoretical basis for the research on the degradation mechanism of biodegradable plastic films. [Method] The effect of illumination intensity on the decomposition of decomposable mulching films was investigated through simulating the field condition in laboratory. Regression analysis was employed to fit the processes of film decompositions. [Result] The weight loss ratios of different types of plastic films were closely related with the illumination. There was no sundry produced during the degradation process, but the weight was reduced, indicating that degradation produced gas, thus, ultraviolet rays had destructive effect on mulch plastic films. Different types of plastic films showed significant differences in the degradation speeds, and under the same conditions, the degradation speed of S4# with the induction period of 30 d was the fastest. With the extension of uv illumination time, the degradation became cumulative degradation process. [Conclusion] Under the uv rays, the weight loss ratio and illumination hours is regarded as a positive correlation relationship. The significant inspection shows that the data fitted degradation model can be described by the logistic model of Y = a/(1+b×e -ct), and all the parameters show significant differences (P0.01).展开更多
Due to the increasing demand for modified polylactide(PLA)meeting“double green”criteria,the research on sustainable plasticizers for PLA has attracted broad attentions.This study reported an open-ring polymerization...Due to the increasing demand for modified polylactide(PLA)meeting“double green”criteria,the research on sustainable plasticizers for PLA has attracted broad attentions.This study reported an open-ring polymerization method to fabricate cellulose(MCC)-g-PCL(poly(ε-caprolactone))copolymers with a fully sustainable and biodegradable component.MCC-g-PCL copolymers were synthesized,characterized,and used as green plasticizers for the PLA toughening.The results indicated that the MCC-g-PCL derivatives play an important role in the compatibility,crystallization,and toughening of the PLA/MCC-g-PCL composites.The mechanical properties of the fully bio-based PLA/MCC-g-PCL composites were optimized by adding 15 wt%MCC-g-PCL,that is,the elongation at break was 22.6%(~376%higher than that of neat PLA),the tensile strength was 47.3 MPa(comparable to that of neat PLA),and the impact strength was 26 J/m(~130%higher than that of neat PLA).DSC results indicated that MCC-g-PCL reduced the Tg of the PLA blend.When the addition amount was 15 wt%,the Tg of the blend was 58.4°C.Compared with MCC,MCC-g-PCL polyester plasticizer has better thermal stability,T5%(°C)can still be maintained above 300°C.The rheological results showed that MCC-g-PCL acted as a plasticizer,the introduction of PCL flexible chain increased the mobility of PLA molecular chain,and decreased the complex viscosity,storage modulus and loss modulus of PLA blends.The MCC-g-PCL derivatives,as a new green plastic additive,have shown an interesting prospect to prepare fully bio-based composites.展开更多
A promising strategy to counteract the progressing plastic pollution of the environment can involve the replacement of persistent plastics with biodegradable materials.Biodegradable polymers are enzymatically degradab...A promising strategy to counteract the progressing plastic pollution of the environment can involve the replacement of persistent plastics with biodegradable materials.Biodegradable polymers are enzymatically degradable by various hydrolytic enzymes.However,these materials can reach the environment in the same way as conventional plastics.Therefore,they are accessible to terrestrial,freshwater,and marine biota.Once ingested by marine organisms,highly active enzymes in their digestive tracts may break down biodegradable compounds.We incubated microparticles of five different biodegradable plastics,based on polylactictic acid(PLA),polybutylene succinate(PBS),polybutylene adipate terephthalate(PBAT)and polyhydroxybutyrate-co-valerate(PHBV),in-vitro with the gastric fluid of the edible crab Cancer pagurus and evaluated the hydrolysis rates by pH Stat titration.A plastic blend of PLA with PBAT showed the highest hydrolysis rate.The enzymes in the gastric fluid of crabs were separated by anion exchange chromatography.Fractions with carboxylesterase activity were identified using fluorescent methylumbelliferyl(MUF)-derivatives.Pooled fractions with high carboxylesterase activity also hydrolyzed a PLA/PBAT plastic blend.Carboxylesterases showed molecular masses of 40–45 kDa as determined by native gel electrophoresis(SDS-PAGE).Our study demonstrated that digestive carboxylesterases in the gastric fluid of C.pagurus exhibit a high potential for hydrolyzing certain biodegradable plastics.Since esterases are common in the digestive tract of organisms,it seems likely that other invertebrates possess the ability to hydrolyze biodegradable plastics.展开更多
Plasticizers are essential additives in the processing of polyvinyl chloride(PVC),with phthalate plasticizers being widely used.However,these conventional plasticizers have been shown to be harmful to human health and...Plasticizers are essential additives in the processing of polyvinyl chloride(PVC),with phthalate plasticizers being widely used.However,these conventional plasticizers have been shown to be harmful to human health and environmentally unfriendly,necessitating the exploration of eco-friendly bio-based alternatives.In this study,Camellia oleifera seed oil,a specialty resource in China,was utilized as a raw material and reacted with 4,4′-Methylenebis(N,N-diglycidylaniline)(AG-80)to synthesize Phenyl Camellia seed Oil Ester(PCSOE).PCSOE was employed as a plasticizer to prepare modified PVC films with varying concentrations,with the conventional plasticizer dioctyl phthalate(DOP)serving as a control.Experimental results demonstrate that PSCOE-plasticized PVC films exhibit enhanced hydrophilicity,tensile strength,and thermal stability compared to DOP-modified PVC films.The contact angle of PSCOE-plasticized PVC films ranges from 66.26°to 78.48°,which is generally lower than the contact angle of DOP-modified PVC films at 78.40°,indicating improved hydrophilicity due to the modification with PCSOE.The tensile strength of PSCOE-plasticized PVC films ranges from 17.73 to 20.17 MPa,all surpassing the value of 16.41 MPa for DOP-modified PVC films.Moreover,the temperatures corresponding to 5%,10%,and 50%weight loss for PVC samples modified with PCSOE are higher than those for DOP.Hence,PCSOE presents a viable alternative to DOP as a plasticizer for PVC materials.展开更多
Polypropene (PP) plastics can be effectively degraded by natural volatile con- stituents from Ledum palustre catalyzed by atmospheric air dielectric barrier (DBD) plasma. The electron spin resonance (ESR) result...Polypropene (PP) plastics can be effectively degraded by natural volatile con- stituents from Ledum palustre catalyzed by atmospheric air dielectric barrier (DBD) plasma. The electron spin resonance (ESR) result indicates that the volatile constituents produce radicals in aerobic condition energized by power sources such as light, UV, plasma and so on. The degradation is a novel chemically oxidative way and it is initiated by a series of radical reactions. Lots of active cud oxidative species, radicals, products cud high euergy electromagnetic field in plasma aggravate the degradation process. The results about PP maximum tensile strength (Crbmax) confirm this conclusion. PP plastic heavily loses its extensibility, mechanical integrity and strength in a short time after suffering a synergetic treatment of the herb extract and air DBD plasma with no toxic residues left. The components of herb extract keep almost unchanged and may be reused. This study offers a new approach to manage and recycle typical plastics.展开更多
Degradable plastic mulch is being used to overcome the negative environmental impacts of burning and landfilling agricultural plastic waste. In this study P. ostreatus was used to model the capacity of a vegetal speci...Degradable plastic mulch is being used to overcome the negative environmental impacts of burning and landfilling agricultural plastic waste. In this study P. ostreatus was used to model the capacity of a vegetal species to degrade conventional and degradable plastic films. Plastics studied were oxo-degradable polyethylene (OXO-PE), UV-irradiated oxo-degradable polyethylene (UV-OXO-PE), polylactic acid (PLA) and conventional polyethylene (C-PE). The cultivation of P. ostreatus resulted in a reduction in the median of weight (78.2% - 80.2%) and volume (56.1% - 60.1%) of the substrate (wheat straw). Degradation of the plastics embodied was evidenced by a reduction in the median of the elongation at break (OXO-PE 475% to 109%, UV-OXO-PE 23% to 8%, PLA 596% to 398% and C-PE 505% to 304%) and an increase in the median of the carbonyl index (OXO-PE 0.062 to 0.114, UV-OXO-PE 0.098 to 0.145 and PLA 0.024 to 0.034). The Kruskal-Wallis test found no statistical difference (p = 0.384) between the medians of the biological efficiency for substrates containing plastics and the substrate without plastic. In conclusion, plastics embodied in the substrates used for cultivation of P. ostreatus are degraded and the degradation of these plastics does not affect the short term growth of P. ostreatus.展开更多
Polystyrene (PS) waste plastic to renewable energy or naphtha grade fuel production through fractional distillation process was applied and PS liquefaction temperature range was 250?C - 430?C and fractional column tem...Polystyrene (PS) waste plastic to renewable energy or naphtha grade fuel production through fractional distillation process was applied and PS liquefaction temperature range was 250?C - 430?C and fractional column temperature was 110?C - 135?C for naphtha grade fuel separation. The thermal degradation of PS waste plastic to renewable energy or naphtha grade chemical production was without adding any kind of cracking catalyst and without vacuum system. Polystyrene waste plastic is not bio-degradable and its can remain long period of landfill and creating gas emission for that reason its major cause climate change. For experimental purpose raw sample was use 1 kg of PS waste plastic and experiment was performed under Labconco fume hood and experiment was fully closed system, whole experiment was performed into stainless steel reactor. Produced fuel was analysis by gas chromatography and mass spectrometer, FT-IR and DSC. Analysis result indicate for fuel compounds chemical structure, compound band energy and enthalpy, delta H value. Produced fuel sulfur content less then environmental protection agency (EPA) level and fuel could be use for chemical feedstock refinery for further modification. By using this technology can reduce some foreign oil dependency and boost up renewable energy sector all over the world.展开更多
In this study,as the plasticizer,Camellia oleifera seed-oil-based cyclohexyl ester(COSOCE)was prepared by the reaction of cyclohexene oxide and refined C.oleifera seed oil(RCOSO)obtained by acidification hydrolysis af...In this study,as the plasticizer,Camellia oleifera seed-oil-based cyclohexyl ester(COSOCE)was prepared by the reaction of cyclohexene oxide and refined C.oleifera seed oil(RCOSO)obtained by acidification hydrolysis after saponification.In addition,the structure of the target product was confirmed by Fourier transform infrared(FTIR)spectroscopy,nuclear magnetic resonance(NMR)spectroscopy,and Raman spectroscopy.COSOCE was used as plasticizer-modified polyvinyl chloride(PVC)membranes.The structure of the COSOCE-modified PVC membranes were characterized by Raman spectroscopy and scanning electron microscopy(SEM).The properties of the COSOCE-modified PVC membrane were characterized by contact angle measurements,universal testing machine,thermogravimetric analysis(TGA),and differential scanning calorimetry(DSC).The results revealed that(1)The COSOCE-modified PVC membranes exhibit a good microscopic morphology.Combined with energy-dispersive X-ray spectroscopy(EDS)and contact angle measurement results,the COSOCE-modified PVC membranes are confirmed to be a hydrophilic material.(2)The modified PVC membrane with 60%COSOCE exhibited the best mechanical properties.The tensile strength reached 23.56±2.94 MPa.(3)COSOCE-modified PVC material exhibited better thermal stability,with a loss rate of less than 75%at the end of the first decomposition stage.Compared with that of the dioctyl-phthalate(DOP)-modified PVC membrane,the initial decomposition temperature of PVC was increased by 1.17°C–8.17°C,and the residual rate was increased by 0.67%–5.75%.The carbon–carbon double bond in the COSOCE molecular structure can remove the free radicals generated during the degradation of PVC material and slow down the decomposition rate of PVC.In addition,the double bond can be cross-linked partially with the PVC molecular chain containing the conjugated polyene structure,thereby increasing the movement resistance of the PVC molecular chain segment.Hence,COSOCE can replace DOP as a PVC plasticizer.展开更多
Aviation fuel is in great demand globally. The increased demand and high price for energy sources are driving efforts to convert natural non-renewable organic compounds into useful hydrocarbon fuel materials such as i...Aviation fuel is in great demand globally. The increased demand and high price for energy sources are driving efforts to convert natural non-renewable organic compounds into useful hydrocarbon fuel materials such as in form of aviation fuel. Alternate sources to these non-renewable hydrocarbon fuels are important and necessary. Much of these alternative sources are focused on biomass however, there are strong benefits of deriving fuels from waste plastic materials. Thermal processes can be used to convert waste plastics into hydrocarbon fuels like aviation fuel, which have unlimited applications in airline industries, as well as in transportation and power generation industries. These thermal processes are used to break down the long carbon chains found in plastics into the shorter chains in a temperature range from 300-450 ℃. This method has been carried out in succession in previous experiments. This simple and economically viable process has been developed to convert the hydrocarbon polymers of waste plastics into the short and medium chain hydrocarbons of liquid fuels. Based on the initial characterization, a fractionated portion of the developed fuel shows properties similar to some of the commercially available aviation fuels.展开更多
基金supported by the National Natural Science Foundation of China(52270132).
文摘Light emitting diodes(LEDs)have accounted for most of the lighting market as the technology matures and costs continue to reduce.As a new type of e-waste,LED is a double-edged sword,as it contains not only precious and rare metals but also organic packaging materials.In previous studies,LED recycling focused on recovering precious and strategic metals while ignoring harmful substances such as organic packaging materials.Unlike crushing and other traditional methods,hydrothermal treatment can provide an environment-friendly process for decomposing packaging materials.This work developed a closed reaction vessel,where the degradation rate of plastic polyphthalamide(PPA)was close to 100%,with nano-TiO_(2)encapsulated in plastic PPA being efficiently recovered,while metals contained in LED were also recycled efficiently.Besides,the role of water in plastic PPA degradation that has been overlooked in current studies was explored and speculated in detail in this work.Environmental impact assessment revealed that the proposed recycling route for waste LED could significantly reduce the overall environmental impact compared to the currently published processes.Especially the developed method could reduce more than half the impact of global warming.Furthermore,this research provides a theoretical basis and a promising method for recycling other plastic-packaged e-waste devices,such as integrated circuits.
文摘Microplastics are persistent anthropogenic pollutants that have become a global concern due to their widespread distribution and unfamiliar threat to the environment and living organisms. Conventional technologies are unable to fully decompose and mineralize plastic waste. Therefore, there is a need to develop an environmentally friendly, innovative and sustainable photocatalytic process that can destroy these wastes with much less energy and chemical consumption. In photocatalysis, various nanomaterials based on wide energy band gap semiconductors such as TiO2 and ZnO are used for the conversion of plastic contaminants into environmentally friendly compounds. In this work, the removal of plastic fragments by photocatalytic reactions using newly developed photocatalytic composites and the mechanism of photocatalytic degradation of microplastics are systematically investigated. In these degradation processes, sunlight or an artificial light source is used to activate the photocatalyst in the presence of oxygen.
基金The work at Harvard University,USA was supported by National Science Foundation(NSF)Materials Research Science and Engineering Centers(MRSEC)(DMR-2011754)X.Yang was a visiting student at Harvard University supported by the China Scholarship Council.J.Steck acknowledges support from the NSF Graduate Research Fellowship(DGE1745303).
文摘A plastic may degrade in response to a trigger.The kinetics of degradation have long been characterized by the loss of weight and strength over time.These methods of gross characterization,however,are misleading when plastic degrades heterogeneously.Here,we study heterogeneous degradation in an extreme form:the growth of a crack under the combined action of chemistry and mechanics.An applied load opens the crack,exposes the crack front to chemical attack,and causes the crack to outrun gross degradation.We studied the crack growth in polylactic acid(PLA),a polyester in which ester bonds break by hydrolysis.We cut a crack in a PLA film using scissors,tore it using an apparatus,and recorded the crack growth using a camera through a microscope.In our testing range,the crack velocity was insensitive to load but was sensitive to humidity and pH.These findings will aid the development of degradable plastics for healthcare and sustainability.
基金Supported by the National Key Technology R&D Program (2007BAC20B01)the Fund for Postgraduate of Tarim University (TDZKSS06004)~~
文摘[Objective] This study aimed to solve the mulch plastic film pollution problems in Xinjiang, in order to provide reliable theoretical basis for the research on the degradation mechanism of biodegradable plastic films. [Method] The effect of illumination intensity on the decomposition of decomposable mulching films was investigated through simulating the field condition in laboratory. Regression analysis was employed to fit the processes of film decompositions. [Result] The weight loss ratios of different types of plastic films were closely related with the illumination. There was no sundry produced during the degradation process, but the weight was reduced, indicating that degradation produced gas, thus, ultraviolet rays had destructive effect on mulch plastic films. Different types of plastic films showed significant differences in the degradation speeds, and under the same conditions, the degradation speed of S4# with the induction period of 30 d was the fastest. With the extension of uv illumination time, the degradation became cumulative degradation process. [Conclusion] Under the uv rays, the weight loss ratio and illumination hours is regarded as a positive correlation relationship. The significant inspection shows that the data fitted degradation model can be described by the logistic model of Y = a/(1+b×e -ct), and all the parameters show significant differences (P0.01).
基金supported by the National Natural Science Foundation of China(21574030,52063007,51863004)Guizhou Province High-Level Innovative Talents Fund([2020]6024)+1 种基金Guizhou Provincial Science and Technology Projects(Grant No.[2022]024)and the Science and Technology Project of Baiyun District,Guiyang City(Grant No.[2020]26)the authors gratefully acknowledge the financial support from the National Engineering Research Center for Compounding and Modification of Polymeric Materials(Guizhou Material Industrial Technology Institute).
文摘Due to the increasing demand for modified polylactide(PLA)meeting“double green”criteria,the research on sustainable plasticizers for PLA has attracted broad attentions.This study reported an open-ring polymerization method to fabricate cellulose(MCC)-g-PCL(poly(ε-caprolactone))copolymers with a fully sustainable and biodegradable component.MCC-g-PCL copolymers were synthesized,characterized,and used as green plasticizers for the PLA toughening.The results indicated that the MCC-g-PCL derivatives play an important role in the compatibility,crystallization,and toughening of the PLA/MCC-g-PCL composites.The mechanical properties of the fully bio-based PLA/MCC-g-PCL composites were optimized by adding 15 wt%MCC-g-PCL,that is,the elongation at break was 22.6%(~376%higher than that of neat PLA),the tensile strength was 47.3 MPa(comparable to that of neat PLA),and the impact strength was 26 J/m(~130%higher than that of neat PLA).DSC results indicated that MCC-g-PCL reduced the Tg of the PLA blend.When the addition amount was 15 wt%,the Tg of the blend was 58.4°C.Compared with MCC,MCC-g-PCL polyester plasticizer has better thermal stability,T5%(°C)can still be maintained above 300°C.The rheological results showed that MCC-g-PCL acted as a plasticizer,the introduction of PCL flexible chain increased the mobility of PLA molecular chain,and decreased the complex viscosity,storage modulus and loss modulus of PLA blends.The MCC-g-PCL derivatives,as a new green plastic additive,have shown an interesting prospect to prepare fully bio-based composites.
基金This work was supported by the European Union's Horizon 2020 research and innovation program(grant agreement number 860407).
文摘A promising strategy to counteract the progressing plastic pollution of the environment can involve the replacement of persistent plastics with biodegradable materials.Biodegradable polymers are enzymatically degradable by various hydrolytic enzymes.However,these materials can reach the environment in the same way as conventional plastics.Therefore,they are accessible to terrestrial,freshwater,and marine biota.Once ingested by marine organisms,highly active enzymes in their digestive tracts may break down biodegradable compounds.We incubated microparticles of five different biodegradable plastics,based on polylactictic acid(PLA),polybutylene succinate(PBS),polybutylene adipate terephthalate(PBAT)and polyhydroxybutyrate-co-valerate(PHBV),in-vitro with the gastric fluid of the edible crab Cancer pagurus and evaluated the hydrolysis rates by pH Stat titration.A plastic blend of PLA with PBAT showed the highest hydrolysis rate.The enzymes in the gastric fluid of crabs were separated by anion exchange chromatography.Fractions with carboxylesterase activity were identified using fluorescent methylumbelliferyl(MUF)-derivatives.Pooled fractions with high carboxylesterase activity also hydrolyzed a PLA/PBAT plastic blend.Carboxylesterases showed molecular masses of 40–45 kDa as determined by native gel electrophoresis(SDS-PAGE).Our study demonstrated that digestive carboxylesterases in the gastric fluid of C.pagurus exhibit a high potential for hydrolyzing certain biodegradable plastics.Since esterases are common in the digestive tract of organisms,it seems likely that other invertebrates possess the ability to hydrolyze biodegradable plastics.
基金funded by the Scarce and Quality Economic Forest Engineering Technology Research Center(2022GCZX002)the Key Lab.of Biomass Energy and Material,Jiangsu Province(Grant No.JSBEM-S-202305).
文摘Plasticizers are essential additives in the processing of polyvinyl chloride(PVC),with phthalate plasticizers being widely used.However,these conventional plasticizers have been shown to be harmful to human health and environmentally unfriendly,necessitating the exploration of eco-friendly bio-based alternatives.In this study,Camellia oleifera seed oil,a specialty resource in China,was utilized as a raw material and reacted with 4,4′-Methylenebis(N,N-diglycidylaniline)(AG-80)to synthesize Phenyl Camellia seed Oil Ester(PCSOE).PCSOE was employed as a plasticizer to prepare modified PVC films with varying concentrations,with the conventional plasticizer dioctyl phthalate(DOP)serving as a control.Experimental results demonstrate that PSCOE-plasticized PVC films exhibit enhanced hydrophilicity,tensile strength,and thermal stability compared to DOP-modified PVC films.The contact angle of PSCOE-plasticized PVC films ranges from 66.26°to 78.48°,which is generally lower than the contact angle of DOP-modified PVC films at 78.40°,indicating improved hydrophilicity due to the modification with PCSOE.The tensile strength of PSCOE-plasticized PVC films ranges from 17.73 to 20.17 MPa,all surpassing the value of 16.41 MPa for DOP-modified PVC films.Moreover,the temperatures corresponding to 5%,10%,and 50%weight loss for PVC samples modified with PCSOE are higher than those for DOP.Hence,PCSOE presents a viable alternative to DOP as a plasticizer for PVC materials.
基金supported by National Natural Science Foundation of China (No.20706060)Specialized Research Fund for the Doctoral Program of Higher Education of China (No.20070425515)+1 种基金Natural Science Foundation of Shandong Province,China (No.Q2007B06)PetroChina Innovation Foundation (No.07E1022)
文摘Polypropene (PP) plastics can be effectively degraded by natural volatile con- stituents from Ledum palustre catalyzed by atmospheric air dielectric barrier (DBD) plasma. The electron spin resonance (ESR) result indicates that the volatile constituents produce radicals in aerobic condition energized by power sources such as light, UV, plasma and so on. The degradation is a novel chemically oxidative way and it is initiated by a series of radical reactions. Lots of active cud oxidative species, radicals, products cud high euergy electromagnetic field in plasma aggravate the degradation process. The results about PP maximum tensile strength (Crbmax) confirm this conclusion. PP plastic heavily loses its extensibility, mechanical integrity and strength in a short time after suffering a synergetic treatment of the herb extract and air DBD plasma with no toxic residues left. The components of herb extract keep almost unchanged and may be reused. This study offers a new approach to manage and recycle typical plastics.
文摘Degradable plastic mulch is being used to overcome the negative environmental impacts of burning and landfilling agricultural plastic waste. In this study P. ostreatus was used to model the capacity of a vegetal species to degrade conventional and degradable plastic films. Plastics studied were oxo-degradable polyethylene (OXO-PE), UV-irradiated oxo-degradable polyethylene (UV-OXO-PE), polylactic acid (PLA) and conventional polyethylene (C-PE). The cultivation of P. ostreatus resulted in a reduction in the median of weight (78.2% - 80.2%) and volume (56.1% - 60.1%) of the substrate (wheat straw). Degradation of the plastics embodied was evidenced by a reduction in the median of the elongation at break (OXO-PE 475% to 109%, UV-OXO-PE 23% to 8%, PLA 596% to 398% and C-PE 505% to 304%) and an increase in the median of the carbonyl index (OXO-PE 0.062 to 0.114, UV-OXO-PE 0.098 to 0.145 and PLA 0.024 to 0.034). The Kruskal-Wallis test found no statistical difference (p = 0.384) between the medians of the biological efficiency for substrates containing plastics and the substrate without plastic. In conclusion, plastics embodied in the substrates used for cultivation of P. ostreatus are degraded and the degradation of these plastics does not affect the short term growth of P. ostreatus.
文摘Polystyrene (PS) waste plastic to renewable energy or naphtha grade fuel production through fractional distillation process was applied and PS liquefaction temperature range was 250?C - 430?C and fractional column temperature was 110?C - 135?C for naphtha grade fuel separation. The thermal degradation of PS waste plastic to renewable energy or naphtha grade chemical production was without adding any kind of cracking catalyst and without vacuum system. Polystyrene waste plastic is not bio-degradable and its can remain long period of landfill and creating gas emission for that reason its major cause climate change. For experimental purpose raw sample was use 1 kg of PS waste plastic and experiment was performed under Labconco fume hood and experiment was fully closed system, whole experiment was performed into stainless steel reactor. Produced fuel was analysis by gas chromatography and mass spectrometer, FT-IR and DSC. Analysis result indicate for fuel compounds chemical structure, compound band energy and enthalpy, delta H value. Produced fuel sulfur content less then environmental protection agency (EPA) level and fuel could be use for chemical feedstock refinery for further modification. By using this technology can reduce some foreign oil dependency and boost up renewable energy sector all over the world.
基金Funding Statement:The authors express their gratitude for the financial support from the National Natural Science Foundation of China(32101475)the Yuemu Technology Plan Project(YMKJ202201).
文摘In this study,as the plasticizer,Camellia oleifera seed-oil-based cyclohexyl ester(COSOCE)was prepared by the reaction of cyclohexene oxide and refined C.oleifera seed oil(RCOSO)obtained by acidification hydrolysis after saponification.In addition,the structure of the target product was confirmed by Fourier transform infrared(FTIR)spectroscopy,nuclear magnetic resonance(NMR)spectroscopy,and Raman spectroscopy.COSOCE was used as plasticizer-modified polyvinyl chloride(PVC)membranes.The structure of the COSOCE-modified PVC membranes were characterized by Raman spectroscopy and scanning electron microscopy(SEM).The properties of the COSOCE-modified PVC membrane were characterized by contact angle measurements,universal testing machine,thermogravimetric analysis(TGA),and differential scanning calorimetry(DSC).The results revealed that(1)The COSOCE-modified PVC membranes exhibit a good microscopic morphology.Combined with energy-dispersive X-ray spectroscopy(EDS)and contact angle measurement results,the COSOCE-modified PVC membranes are confirmed to be a hydrophilic material.(2)The modified PVC membrane with 60%COSOCE exhibited the best mechanical properties.The tensile strength reached 23.56±2.94 MPa.(3)COSOCE-modified PVC material exhibited better thermal stability,with a loss rate of less than 75%at the end of the first decomposition stage.Compared with that of the dioctyl-phthalate(DOP)-modified PVC membrane,the initial decomposition temperature of PVC was increased by 1.17°C–8.17°C,and the residual rate was increased by 0.67%–5.75%.The carbon–carbon double bond in the COSOCE molecular structure can remove the free radicals generated during the degradation of PVC material and slow down the decomposition rate of PVC.In addition,the double bond can be cross-linked partially with the PVC molecular chain containing the conjugated polyene structure,thereby increasing the movement resistance of the PVC molecular chain segment.Hence,COSOCE can replace DOP as a PVC plasticizer.
文摘Aviation fuel is in great demand globally. The increased demand and high price for energy sources are driving efforts to convert natural non-renewable organic compounds into useful hydrocarbon fuel materials such as in form of aviation fuel. Alternate sources to these non-renewable hydrocarbon fuels are important and necessary. Much of these alternative sources are focused on biomass however, there are strong benefits of deriving fuels from waste plastic materials. Thermal processes can be used to convert waste plastics into hydrocarbon fuels like aviation fuel, which have unlimited applications in airline industries, as well as in transportation and power generation industries. These thermal processes are used to break down the long carbon chains found in plastics into the shorter chains in a temperature range from 300-450 ℃. This method has been carried out in succession in previous experiments. This simple and economically viable process has been developed to convert the hydrocarbon polymers of waste plastics into the short and medium chain hydrocarbons of liquid fuels. Based on the initial characterization, a fractionated portion of the developed fuel shows properties similar to some of the commercially available aviation fuels.