Biodegradation Behavior of PLA/PBS Blends

2013 ◽  
Vol 821-822 ◽  
pp. 937-940 ◽  
Author(s):  
Shi Jie Zhang ◽  
Yi Wen Tang ◽  
Li Hua Cheng

Poly (butylene succinate) (PBS) was mixed with Poly (lactic acid) (PLA) in the melt state. The PLA/PBS blends with different constitution were produced. The samples were buried in laterite. Samples were dug out of soil after the burial for 10, 20, 30, 40, 50 and 60 days, respectively. The weight loss and molecular weight of the sample were tested. The analysis showed that the nearly exponential decrease in average molecular weight as a function of degradation time. The PLA and PBS have the similar degradation behavior in the soil.

2013 ◽  
Vol 821-822 ◽  
pp. 941-944
Author(s):  
Shi Jie Zhang ◽  
Yi Wen Tang ◽  
Li Hua Cheng

Poly (butylene succinate) (PBS) was mixed with Poly (lactic acid) (PLA) through Haake Reomix, a new type of biodegradable materials can be obtained. With the increasing addition of PBS and the raise of the solution basicity, the degradation rate of blends increase sharply. The GPC analysis can approve the reduction of molecular weight in the degradation process of PLA/PBS blends.


Author(s):  
Mujtahid Kaavessina ◽  
Chitra Husnabilqis ◽  
Meylani Tri Hardiyanti

<p>Poly lactic acid is a polymer that has been developed as an alternative to substitution of conventional polymers. The properties of this polymer are biodegradable in nature and non-toxic substances. These polymers potentially can be used as a matrix for urea carries. The aim of this research was to synthesize poly lactic acid in a low molecular weight. This product can be used as a matrix that urea release controller during the process of fertilization. The methodology consisted of two stages. The first stage was polycondensation of lactic acid and degradability test. Lactic acid was mixed with SnCl2 catalyst 0.1% and heated to 138oC for 24 hours. The second stage was producing in the form of Smart Urea Controlled Release Nitrogen Fertilizer (CRNF). Urea was dissolved in poly lactic acid through a heating process at 150°C to dissolve urea with variation in urea concentration weight of  0.5%; 0.1%; 0.15%; 0.2%; 0.25%; 0.3% and CRNF granulation processes. Finally, the mixture was granulated in ambient temperature. Chemical analysis was done the molecular weight of poly lactic acid. The relationship between intrinsic viscosity  and  molecular  weight  was  used.  The  IR  spectra  (FTIR)  was  used  to  fine molecular structure. The release testing of urea from the matrix of poly lactic acid uses UV-VIS Spectrophotometer. The results showed that the average molecular weight of poly lactic acid is 1149.49 g /gmol. FTIR spectra of CRNF with variation in urea concentration weight showed the presence of groups owned by poly lactic acid and urea. The peaks are</p><p>1627.03 to 1629.92 cm-1 for the -NH group and 3478.77 to 3498.06 cm-1 for group -OH. The existence of these groups proves the existence of urea in CRNF. The release of urea from poly lactic acid occurs by diffusion. It can be seen, when urea in CRNF form immersed in water, the concentration of urea in water increase as well as the increasing immersed time.</p>


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Chenguang Liu ◽  
Yuliang Jia ◽  
Aihua He

High molecular weight poly (lactic acid) (PLA) was obtained by chain extending with hexamethylene diisocyanate (HDI). The influences of the amount of chain extender, reaction time, and molecular weight changes of prepolymers on the poly(lactic acid) were investigated. PLA prepolymer with a viscosity, average molecular weight (Mη) of 2 × 104 g/mol was synthesized froml-lactide using stannous octoate as the catalyst. After 20 min of chain extension at 175°C, the resulting polymer hadMwof 20.3 × 104 g/mol andMnof 10.5 × 104 g/mol. Both FT-IR and1H-NMR verified that the structure of PLA did not change either before chain extending or after. The optically active characterized that the chain extending-product was left handed. DSC and XRD results showed that both theTgand the crystallinity of PLA were lowered by chain-extension reaction. The crystalline transformation happened in PLA after chain extending, crystallineα′form toαform.


2011 ◽  
Vol 410 ◽  
pp. 337-340
Author(s):  
Suek Songprateepkul ◽  
Suriyan Rakmae ◽  
C. Deeprasertkul ◽  
Nitinat Suppakarn ◽  
Pranee Chumsamrong

In this work, hydroxyl-terminated lactic acid prepolymer was firstly prepared by adding diethylene glycol in the condensation of lactic acid. Molecular weight, acid value and structure of prepolymer were characterized. The results showed that the prepolymer was hydroxyl-terminated with weight average molecular weight (MW) of 10,000 g/mol. After that, the chain linking polymerization of the prepolymer was carried out in a glass tube at 160 °C for 1 h employing 1,6-hexamethylene diisocyanate (HMDI) as a chain extender. By varying the hydroxyl/isocyanate ratio, it was found that the OH/NCO ratio of 1:2 seemed to be the most suitable ratio which gave PLA with the maximum MW of 93,000 g/mol.


2018 ◽  
Vol 6 (2) ◽  
pp. 626
Author(s):  
Irwan Noezar ◽  
V.S. Praptowidodo ◽  
R. Nugraheni ◽  
M.H. Nasution

The objective of this research is to learn and to make the biodegradable polymer, Poly(lactic acid), from lactic acid by condensation polymerization without catalyst. Poly(lactic acid) that will be produced in this research should have the molecular weight between 3000-5000 grams/mole. The scopes of this research are the_purification of lactic acid, purity analysis, polymerization reaction, and polymer's characteristic analysis. The method of lactic acid purification is distillation in nitrogen atmosphere. Polymerization reaction which is used in this research is the condensation polymerization without catalyst. The polymer's characteristics that will be analyzed are molecular weight and  degradation time Molecular weight is analyzed by viscosimetry method and Gel Permeation Chromatography. Degradation time is analyzed by landfill method Based on this research, purification of D,L-lactic acid (91%-weight) reaches 98%-weight and for L-lactic acid (93%-weight) reaches 96%-berat. Molecular weight of D,L-lactic acid between 450-3600 grams/mole and L-lactic acid between 4200-8500 grams/mole.  The degradation time of polymer is 5 weeks.Keywords: Poly(lactic acid), polymer,  biodegradable AbstrakPenelitian ini bertujuan untuk mempelajari dan mensintesis biodegradable polymer, Poly(lactic acid) dari asam laktat melalui reaksi polimerisasi kondensasi tanpa katalis. Poly(lactic acid) yang dihasilkan dalam penelitian ini diharapkan memiliki berat molekul antara 3000-5000 gram/mol. Ruang lingkup penelitian meliputi pemurnian asam laktat, analisa kemurnian asam laktat, reaksi polimerisasi kondensasi dan karakterisasi polimer. Pemurnian asam laktat dilakukan melalui distilasi pada atmosfer nitrogen dan tekanan 1 atmosfer. Reaksi polimerisasi dilakukan melalui polimerisasi kondensasi tanpa katalis dengan variasi waktu reaksi pengadukan mekanik dan laju pemanasan. Karakteristik polimer yang dianalisis adalah berat molekul dan waktu degradasi. Berat molekul dianalisis dengan metode GPC (Gel Permeation Chromatography) dan viskosimetri. Degradasi polimer dilakukan secara landfill. Berdasarkan hasil percobaan, pemurnian asam laktat untuk monomer D,L-Lacticacid (91%-berat) mencapai 98%-berat sedangkan untuk monomer L-Lactic acid (93%-berat) mencapai 96%-berat. Berat molekul yang dihasilkan untuk monomer D,L-Lactic acid adalah 450 - 3600 gram/mol sedangkan untuk monomer L-Lactic acid adalah 4200- 8500 gram/mol. Waktu degradasi polimer secara landfill adalah 5 minggu.Kata kunci : Poly(lactic acid), polimer, biodegradable


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1822
Author(s):  
Evangelia Balla ◽  
Vasileios Daniilidis ◽  
Georgia Karlioti ◽  
Theocharis Kalamas ◽  
Myrika Stefanidou ◽  
...  

Environmental problems, such as global warming and plastic pollution have forced researchers to investigate alternatives for conventional plastics. Poly(lactic acid) (PLA), one of the well-known eco-friendly biodegradables and biobased polyesters, has been studied extensively and is considered to be a promising substitute to petroleum-based polymers. This review gives an inclusive overview of the current research of lactic acid and lactide dimer techniques along with the production of PLA from its monomers. Melt polycondensation as well as ring opening polymerization techniques are discussed, and the effect of various catalysts and polymerization conditions is thoroughly presented. Reaction mechanisms are also reviewed. However, due to the competitive decomposition reactions, in the most cases low or medium molecular weight (MW) of PLA, not exceeding 20,000–50,000 g/mol, are prepared. For this reason, additional procedures such as solid state polycondensation (SSP) and chain extension (CE) reaching MW ranging from 80,000 up to 250,000 g/mol are extensively investigated here. Lastly, numerous practical applications of PLA in various fields of industry, technical challenges and limitations of PLA use as well as its future perspectives are also reported in this review.


Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2531
Author(s):  
Rodion Kopitzky

Sugar beet pulp (SBP) is a residue available in large quantities from the sugar industry, and can serve as a cost-effective bio-based and biodegradable filler for fully bio-based compounds based on bio-based polyesters. The heterogeneous cell structure of sugar beet suggests that the processing of SBP can affect the properties of the composite. An “Ultra-Rotor” type air turbulence mill was used to produce SBP particles of different sizes. These particles were processed in a twin-screw extruder with poly(lactic acid) (PLA) and poly(butylene succinate) (PBS) and fillers to granules for possible marketable formulations. Different screw designs, compatibilizers and the use of glycerol as a thermoplasticization agent for SBP were also tested. The spherical, cubic, or ellipsoidal-like shaped particles of SBP are not suitable for usage as a fiber-like reinforcement. In addition, the fineness of ground SBP affects the mechanical properties because (i) a high proportion of polar surfaces leads to poor compatibility, and (ii) due to the inner structure of the particulate matter, the strength of the composite is limited to the cohesive strength of compressed sugar-cell compartments of the SBP. The compatibilization of the polymer–matrix–particle interface can be achieved by using compatibilizers of different types. Scanning electron microscopy (SEM) fracture patterns show that the compatibilization can lead to both well-bonded particles and cohesive fracture patterns in the matrix. Nevertheless, the mechanical properties are limited by the impact and elongation behavior. Therefore, the applications of SBP-based composites must be well considered.


2015 ◽  
Vol 133 (8) ◽  
pp. n/a-n/a ◽  
Author(s):  
Weraporn Pivsa-Art ◽  
Kazunori Fujii ◽  
Keiichiro Nomura ◽  
Yuji Aso ◽  
Hitomi Ohara ◽  
...  

2017 ◽  
Vol 872 ◽  
pp. 165-170
Author(s):  
Shi Chao Lu ◽  
Yang Chuan Ke ◽  
Qian Zhou ◽  
Zhao Rui Meng ◽  
Guo Liang Zhang ◽  
...  

The carboxyl terminated poly (L-lactic acid) (PLLA) prepolymers were prepared via polycondensation of L-lactic acid and 1,6-adipic acid (end capping agent) under the catalyst of stannous octoate. The effects of synthetic condition, such as reaction temperature, amount of catalyst, content of the end capping agent, etc, on the molecular weight of PLLA were discussed. Fourier transform infrared and 1H nuclear magnetic resonance were used to characterize the PLLA prepolymers. The results indicated that the polycondensation was performed under an optimum reaction condition as following: the amount of the catalyst was 500 ppm based on the mass of lactic acid, the amount of the end capping agent was 1% (the molar amount of the lactic acid), and the polymerization temperature was 170 °C. The viscosity-average molecular weight of the product reached 2.826×104 at this polymerization temperature and the yield was 73.34%.


2016 ◽  
Vol 19 (4) ◽  
pp. 58-65
Author(s):  
Ha Thi Thai La

In this research, the PLA-diol were synthesized from lactic acid (LA) and 1.4 butanediols (BD) with a tin octoate Sn(Oct)2 catalyst at a temperature of 180 °C and the pressure 5 mmHg. The structure and properties of PLA-diol are analyzed by the following methods: GPC, 1H-NMR and DSC. As a result, with the change in the content of Sn (Oct)2 from 0.1 to 1.0%, the molecular weight Mn of PLA - diol increased gradually from 4.119,2 to 7.359,6 g / mol . In addition, the BD content increased from 2.0% to 5.0%, the average molecular weight of the product decreased gradually from 7.536,9 g / mol to 4.735 g / mol, respectively. This change will affect the ability to use PLA-diol in the next denaturation research to apply in the field of biodegradable polymer such as copolymer with polyurethane, copolymer with polyethylene glycol diacid, or chain extension with other polymer in a chain reaction,...


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