scholarly journals Smart-Urea-Controlled-Release-Nitrogen-Fertilizer Menggunakan Plastik Biodegradable Poli Asam Laktat Sebagai Carrier

2017 ◽  
Vol 1 (2) ◽  
Author(s):  
Mujtahid Kaavessina ◽  
Chitra Husnabilqis ◽  
Meylani Tri Hardiyanti
Keyword(s):  
Molecular Weight ◽  
Lactic Acid ◽  
Controlled Release ◽  
Nitrogen Fertilizer ◽  
Average Molecular Weight ◽  
Urea Concentration ◽  
Poly Lactic Acid ◽  
Heating Process ◽  
Toxic Substances ◽  
The Matrix

<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>

Biodegradation Behavior of PLA/PBS Blends

2013 ◽  
Vol 821-822 ◽  
pp. 937-940 ◽  
Author(s):  
Shi Jie Zhang ◽  
Yi Wen Tang ◽  
Li Hua Cheng
Keyword(s):  
Molecular Weight ◽  
Weight Loss ◽  
Lactic Acid ◽  
Average Molecular Weight ◽  
Poly Lactic Acid ◽  
Degradation Behavior ◽  
Butylene Succinate ◽  
Exponential Decrease ◽  
Degradation Time

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.

scholarly journals Preparation of Higher Molecular Weight Poly (L-lactic Acid) by Chain Extension

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Chenguang Liu ◽  
Yuliang Jia ◽  
Aihua He
Keyword(s):  
Molecular Weight ◽  
Lactic Acid ◽  
Average Molecular Weight ◽  
Hexamethylene Diisocyanate ◽  
Chain Extension ◽  
Poly Lactic Acid ◽  
Weight Changes ◽  
H Nmr ◽  
Left Handed ◽  
Ft Ir

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.

The Preparation of Poly(lactic acid) via Chain Linked Hydroxy-Terminated Lactic Acid Prepolymer

2011 ◽  
Vol 410 ◽  
pp. 337-340
Author(s):  
Suek Songprateepkul ◽  
Suriyan Rakmae ◽  
C. Deeprasertkul ◽  
Nitinat Suppakarn ◽  
Pranee Chumsamrong
Keyword(s):  
Molecular Weight ◽  
Lactic Acid ◽  
Average Molecular Weight ◽  
Glass Tube ◽  
Acid Value ◽  
Chain Extender ◽  
Hexamethylene Diisocyanate ◽  
Poly Lactic Acid ◽  
Weight Average Molecular Weight ◽  
A Chain

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.

scholarly journals Poly(lactic Acid): A Versatile Biobased Polymer for the Future with Multifunctional Properties—From Monomer Synthesis, Polymerization Techniques and Molecular Weight Increase to PLA Applications

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1822
Author(s):  
Evangelia Balla ◽  
Vasileios Daniilidis ◽  
Georgia Karlioti ◽  
Theocharis Kalamas ◽  
Myrika Stefanidou ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Lactic Acid ◽  
Chain Extension ◽  
Poly Lactic Acid ◽  
Plastic Pollution ◽  
Practical Applications ◽  
Decomposition Reactions ◽  
Melt Polycondensation ◽  
Polymerization Conditions ◽  
Molecular Weight Increase

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.

Study on the Preparation and Characterization of Carboxyl Terminated Poly(L-Lactic Acid) (PLLA) Prepolymers

2017 ◽  
Vol 872 ◽  
pp. 165-170
Author(s):  
Shi Chao Lu ◽  
Yang Chuan Ke ◽  
Qian Zhou ◽  
Zhao Rui Meng ◽  
Guo Liang Zhang ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Lactic Acid ◽  
Average Molecular Weight ◽  
Polymerization Temperature ◽  
Capping Agent ◽  
Molar Amount ◽  
Optimum Reaction ◽  
Catalyst Content ◽  
End Capping

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%.

scholarly journals Synthesis of polylactic acid-diol (PLA-diol) from lactic acid and 1,4-butanediol

2016 ◽  
Vol 19 (4) ◽  
pp. 58-65
Author(s):  
Ha Thi Thai La
Keyword(s):  
Molecular Weight ◽  
Lactic Acid ◽  
Polyethylene Glycol ◽  
1H Nmr ◽  
Biodegradable Polymer ◽  
Average Molecular Weight ◽  
Chain Extension ◽  
Structure And Properties ◽  
Chain Reaction ◽  
A Chain

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,...

scholarly journals Release of Graphene and Carbon Nanotubes from Biodegradable Poly(Lactic Acid) Films during Degradation and Combustion: Risk Associated with the End-of-Life of Nanocomposite Food Packaging Materials

Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2346 ◽  
Author(s):  
Stanislav Kotsilkov ◽  
Evgeni Ivanov ◽  
Nikolay Vitanov
Keyword(s):  
Risk Assessment ◽  
Carbon Nanotubes ◽  
Lactic Acid ◽  
Food Packaging ◽  
Safety Concern ◽  
Barrier Properties ◽  
Nanocomposite Films ◽  
Poly Lactic Acid ◽  
Qualitative Risk Assessment ◽  
The Matrix

Nanoparticles of graphene and carbon nanotubes are attractive materials for the improvement of mechanical and barrier properties and for the functionality of biodegradable polymers for packaging applications. However, the increase of the manufacture and consumption increases the probability of exposure of humans and the environment to such nanomaterials; this brings up questions about the risks of nanomaterials, since they can be toxic. For a risk assessment, it is crucial to know whether airborne nanoparticles of graphene and carbon nanotubes can be released from nanocomposites into the environment at their end-life, or whether they remain embedded in the matrix. In this work, the release of graphene and carbon nanotubes from the poly(lactic) acid nanocomposite films were studied for the scenarios of: (i) biodegradation of the matrix polymer at the disposal of wastes; and (ii) combustion and fire of nanocomposite wastes. Thermogravimetric analysis in air atmosphere, transmission electron microscopy (TEM), atomic force microscopy (AFM) and scanning electron microscope (SEM) were used to verify the release of nanoparticles from nanocomposite films. The three factors model was applied for the quantitative and qualitative risk assessment of the release of graphene and carbon nanotubes from nanocomposite wastes for these scenarios. Safety concern is discussed in respect to the existing regulations for nanowaste stream.

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