Synthesis and properties of novel aliphatic polycarbonate from carbon dioxide with 1,2-butylene oxide and ε-caprolactone

A new degradable aliphatic poly(butylene-co-e-caprolactone carbonate) (PBCL) was synthesized through the terpolymerization of carbon dioxide, 1,2-butylene oxide (BO) and e-caprolactone (CL), a polymer supported bimetallic complex (PBM) was used as a catalyst. The terpolymers prepared were characterized by FT-IR,1H NMR, 13C NMR, WXRD and DSC. The hydrolysis tests were carried out to appraise the degradability of the copolymers.

An Experimental Study of Bulge-Forming Polycarbonate (PC)Semisphere Shell Parts

In this paper, a new bulge-forming technology is described to manufacture a polycarbonate semisphere shell. Some experiments have been done, and the experimental results show that this technique is feasible to form polycarbonate part. But the wall thickness distribution of the bulged specimen by this method is not so even.

Polycarbonate/Polypropylene/Fibrillar Silicate Ternary Nanocomposites: Morphology and Mechanical Properties

Polycarbonate （pc）/polypropylene （pp）/silicate attapulgite （AT） ternary nanocomposites were first prepared via the two-step melt blending process. Phase structure of the ternary composites was characterized by transmission electron microscopy （TEM） and dynamic mechanical analysis （DMA）, in which the morphology of encapsulation of AT by PP in the PC matrix were observed. The mechanical properties of the ternary composites were investigated using the tensile tester and Izod impact tester. The results show that encapsulation of AT by PP in PC enhances the toughness of the matrix effectively and give the best tensile and impact strength.

Preparation of Indium Tin Oxide Films on Polycarbonate substrates by Radio-frequency Magnetron Sputtering

Indium tin oxide（ITO）thin films（100±10nm）were deposited on PC（polycarbonate）and glass substrates by rf（radio-frequency）mannetron spuutering.The oxygen content of the ITO films was changed by variation of the sputtering gas composition.All the other deposition parameters were kept constant.The sheet resistance.optical transmittance and microstructure of ITO films were investigated using a four-point probe.spectrophotometer,X-ray diffractometer（XRD）and atomic force microscope（AFM）.Sheet resistances for the ITO films with optical transmittance more than 75% on PC substrates varied from 40Ω/cm^2 to more than 104 Ω/cm^2 with increasing oxygen partial pressure from O to about 2%.The same tendeney of sheet resistances increasing with increasing oxygen partial pressure was observed on glass substrates.The X-ray diffraction data indicated polycrystalline filns with grain orientations predominantly along（440）and （422）directions.The intensities of （440）and （422）peaks increased slightly with the increase of oxygen partial pressure both on PC and glass substrates.The AFM images show that the ITO films on PC substrates were dense and uniform.The average grain size of the films was about 40nm.

STUDIES ON MISCIBILITY OF POLY (ε-CAPROLACTONE) AND ALIPHATIC POLYCARBONATE BLENDS AND DETERMINATION OF THEIR INTERACTION PARAMETER

In this paper the miscibility of poly (ε-caprolactone) (PCL) and aliphatic polycarbonate (APC) is studied by using DSC. The results show that PCL and APC are miscible in all ranges of composition. The interaction parameter between the polymers is calculated from the melting point depression data. Using optical microscope, the shapes of the PCL spherulites in the blends are observed.

NMR IMAGING OF ACETONE DIFFUSION PROCESS IN POLYCARBONATE

Acetone diffusion in polycarbonate was investigated by spin-echo ~1H NMR imaging method at room temperature. The result shows that the diffusion process satisfies Case Ⅱ diffusion. The velocity of diffusion front is 13.8nm sec^(-1)(0.05mm/h).

Differential Scanning Calorimetry Study of Polyamide 6/Polycarbonate

Blends of polyamide 6 and polycarbonate were prepared by a Brabender mixer （ PLV- 151） at 240 ℃ with 30 rpm for time 15, 8 and 6 minutes respectively. The thermal properties of blends with constituent ratio of 100/0, 60/40 and 20/80 are examined by Differential scanning calorimetry. DSC measures the temperatures and heat flow associated with transitions in materials as a function of time and temperature. The melting point temperature （Tm）, crystalline temperature （Tc）, and glass transition temperature （Tg） are observed.

Rheological properties of novel thermo-responsive polycarbonates aqueous solutions

Thermo-responsive multiblock polycarbonates were facilely synthesized by covalently binding poly(ethylene glycol)(PEG) and poly(propylene glycol)(PPG) blocks,using triphosgene as coupling agent and pyridine as catalyst.The aqueous solutions of thermo-responsive polycarbonates were investigated by rheological measurements.Steady-state shear measurements reveal that the polycarbonate solutions exhibit shear-thinning behavior and the hydrophilic content has a pronounced effect on the flow behavior of the polycarbonates aqueous solutions.The shear viscosity decreases with increasing poly(ethylene oxide)(PEO) composition.The increase of viscosity with increasing concentration is probably attributed to the formation of stronger network owing to interchain entanglement of PEO block at higher concentration.When the flow curves are fitted to the power law model,flow index is obtained to be less than 1,as exhibiting typical pesudoplastic fluid.The viscoelastic properties of the system also show close dependence on the composition of polycarbonates.Temperature sweep confirms that the multiblock polycarbonates exhibit thermo-responsive properties.For 7% aqueous solution of polycarbonate with composition ratio of EO to PO of 1/1,the sol-gel transition occurs at 37 ℃,which makes the system suitable as an injectable drug delivery system.

Morphology and Compatibility of Compatibilized Polyethersulfone and Polycarbonate Blends

A PES-PC （polyethersulfone-polycarbonate） multi block random copolymer was synthesized with two oligomers, polyethersulfone and polycarbonate. The effects of the copolymer, as a compatibilizer, on the morphology and compatibility of the PES-PC blends were investigated. It was found that the addition of this copolymer to the PES-PC blends could improve their compatibility.

Synthesis and Characterization of Novel Aliphatic Polycarbonates Bearing Pendant Allyl Ether Groups

A new six-membered cyclic carbonate monomer, 5-allyloxytrimethylene carbonate （ATMC）, was synthesized starting from glycerol, and the corresponding polycarbonates, poly（5-allyloxytrimethylene carbonate）（PATMC） were further synthesized by ring-opening polymerization in bulk at 150℃ using stannous octanoate as an initiator. The structures of the monomer and the polymers were confirmed by IR, IH-NMR, 13C-NMR, and GPC analysis.

Study of Flame Retardation of Polycarbonate Modified by Polyhedral Oligomeric Silsesquioxane and Caged Bicyclic Phosphate

The flame-retarded polycarbonate（PC） has been made with octaphenyl polyhedral silsesquioxane（OPS） and/or caged bicyclic phosphate（Trimer）.Thermal gravimetric analysis（TGA）,Fourier-transform infrared（FTIR）,TGA-FTIR,limiting oxygen index（LOI）,and mechanical tests have been employed to characterize the modified PC.The additives of OPS and Trimer in PC have been proved to be effective flame-retardants because of the synergistic interaction between the elements of P and Si.The role of OPS and Trimer in PC degradation are different：OPS participates in the charring of PC,while Trimer makes PC degrade in advance.In addition,OPS and Trimer induced obvious differences in the mechanical properties of PC.

Research on relationship between geometrical dimensions and elongation of Polycarbonate tensile specimen

To provide convenience for the translation among specimens,orthogonal experimental method was used to research the relationship between geometrical dimensions(length,width and thickness) and total elongation of polycarbonate sheet,and simulations of tensile specimens with different geometrical dimensions had been conducted by the finite element method,then regression analysis method was used to create the relationship formula between geometrical dimensions and total elongation.It was found that:the shorter the length of specimen is,the better the plasticity is,and they had the power exponent relationship;the larger the width and thickness are,the better the plasticity is,and they had the direct proportion relationship with the total elongation.

MODIFICATION OF SURFACE MECHANICAL PROPERTIES OF POLYCARBONATE BY B^+ AND O^+ IONS IMPLANTATION

By implanting B+ and O+ ions respectively into polycarbonate (PC) plates, the surface mechanical properties of PC have been improved. Measurement by Nano Indenter II showed that the hardness of samples increased 7-25 times than that before implantation; and the modulus of elasticity raised 2-5 times. The wear-resistance was tested by ball crusher; the width and depth of the wear-streak decreased by 1/3-1/2 or even more. The structure, deformation and appearance were analyzed by using Micro-FTIR Spectra, ESCA method and the steps instrument. These analyses showed that the structure of PC had been modified: a series of new cross-linking yielded, it depends on the Linear Energy Transition (LET) of implanted ions in the high polymer compounds.

Unveiling chain–chain interactions in CO2-based crystalline stereocomplexed polycarbonates by solid-state NMR spectroscopy and DFT calculations

CO2-based stereocomplexed polycarbonates derived from the intermolecularly interlocked interaction between the enantiopure polymers with the opposite configuration exhibit high crystallinity, excellent thermal and mechanical stabilities. Deep insights into the mechanism of stereocomplexation are of particular importance to the design and manufacture of new promising and sustainable polycarbonates with enhanced physicochemical properties. Our solid-state NMR experiments linking with DFT computations clearly reveal the specific chain-chain interactions in a typical stereocomplexed poly（4,4-dimethyl-3,5,8-trioxabicyclo[5.1.0] octane carbonate）（PCXC）.13C CP/MAS NMR,1H DUMBO MAS NMR and 13C/1H relaxation-time measurements indicate that the formation of stereocomplex reduces the local mobilities of carbonyl, methine and methylene groups in each chain of PCXC significantly. Through a combination of two-dimensional 1H-13C HETCOR NMR and DFT calculation analysis, the cis-/trans-conformations and packing models of PCXC chains in the amorphous, enantionpure isotactic and stereocomplexed polycarbonates are identified. The splitting of 13C and 1H NMR chemical shifts of methine groups in the backbone carbon region demonstrates the ordered interlock interactions between the R-and S-chain in the stereocomplexed PCXC.

Metal-free synthesis of amphiphilic functional polycarbonates

Amphiphilic block copolymers of poly（5-benzyloxy trimethylene carbonate） （PBTMC） and poly（ethylene glycol） （PEG） were synthesized through enzymatic polymerization using immobilized porcine pancreas lipase （IPPL）. The obtained copolymers with different compositions were characterized by GPC and IH NMR. The copolymer composition was in agreement with the feed ratio. The molecular weight of the copolymers showed an increasing trend with the decrease of PEG contents. MiceUes of the copolymers were formed by dialysis procedure, and characterized by transmission electron microscopy （TEM）.

Enzymatic Synthesis and Characterization of Novel Polycarbonates Derived from 5-Allyloxy-1, 3-dioxan-2-one and 5, 5-Dimethvl-1.3-dioxan-2-one

Novel polycarbonates from 5-allyloxy-1, 3-dioxan-2-one （ATMC） with 5, 5-dimethyl- 1, 3-dioxan-2-one （DTC） were successfully synthesized for the first time using immobilized porcine pancreas lipase （IPPL） as catalyst. The resulting copolymers were characterized by IR, ^1H NMR, ^13C NMR and GPC. The molecular weight （Mn） of the copolymer with molar feed ratio of 10：90 （ATMC：DTC） was 9300 and the polydispersity was 1.31, while the Mn increased to 14300 and polydispersity of 1.25 with the feed ratio of 50：50. Moreover, the composition of the copolymers agreed well with the monomer feed.

Frequency dependence of the electrical conductivity and dielectric constants of polycarbonate (Makrofol-E) film under the effects of γ-radiation

Irradiation effects of γ-radiation on the physical and electrical properties of polycarbonate (Makrofol-E( film has been studied to be able to investigate the dielectric response of irradiated polymers for a wide range of fluence and frequency. The dielectric constant (ε') The loss tangent (tanδ), dielectric loss factor (ε''), the a.c electrical conductivity (σ) and the relaxation time (τ), were measured in the frequency range from (40) Hz to (4) MHz. These samples were irradiated by means of γ-rays from 10 up to 200 KGy. The change in different properties as a function of absorbed dose was studied. Degradation of the polymers leading to amorphisation was observed by increasing the absorbed γ- dose. The induced changes in the electrical conductivity due to γ-rays irradiation of Makrofol-E provide a better method for γ -dose measurements. A semi-empirical equation was developed to use Makrofol-E as a dielectric dosimeter. Furthermore, Makrofol-E has much greater resistance to radiation damage;the attained results suggested strongly the applicability of Makrofol-E to be used in medical products applications.

A Generic Polycarbonate Based Microfluidic Tool to Study Crystal Nucleation in Microdroplets

Crystal nucleation is important to control the product properties in industrial crystallization processes. To investigate crystallization phenomena, methods which rely on microscopic volumes have gained relevance over the last decade. Microfluidic devices are suitable for carrying out crystallization experiments based on a large set of individual droplets in the nanoliter range. In this work, we propose a simple method to manufacture such devices from polycarbonate as an alternative to conventional chips made of poly (dimethylsiloxane). The microfluidic device consists of two main functional parts: A T-junction for droplet generation and a section for storage and observation of up to 400 individual droplets. Using these manufactured devices, it is easy to produce and store highly monodisperse droplets of substances that require either a hydrophilic or hydrophobic surface of the microchannel. Since crystal nucleation is a stochastic process which depends on the sample volume, a reproducible droplet volume is of great importance for crystallization experiments. The versatile applicability of the manufactured devices is demonstrated for substances which are used in different crystallization applications, for example, solution crystallization (aqueous potassium nitrate solution) and melt crystallization (ethylene glycol distearate). Finally, we demonstrate that the manufactured microfluidic devices in our experimental setup can be used to conduct crystal nucleation measurements. Based on these measurements we discuss our results with respect to state-of-the-art nucleation models.