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"Penggunaan plastik terus meningkat, menghasilkan peningkatan limbah plastik. Pada 2015, limbah dari industri pengemasan menghasilkan 141 juta ton. Pada tahun yang sama, produksi berjumlah hingga 381 juta ton, naik 3,6% dari 2014, dari 367 juta ton. Maka itu, diusulkan agar plastik sachet, yang terbuat dari polypropylene (PP), digunakan sebagai sumber karbon alternative untuk sintesis carbon nanotube (CNT). Sebelum melanjutkan dengan sintesis carbon nanotubes (CNT) menggunakan plastic sachet, sangat penting untuk menghilangkan warna dari limbah PP. Penghilangan warna dilakukan dengan merendam plastik sachet di dalam reagen hidrogen peroksida (H2O2). Sintesis CNT dengan sintesis nyala dicoba. Sintesis memanfaatkan SS 316 sebagai substrat katalis, setelah mengalami perlakuan panas oksidatif, selama 30 menit pada suhu 800oC, sebagai metode pra-perlakuan katalis. Hasil karakterisasi dari XRD, SEM-EDS dan TEM, menggambarkan bahwa PP yang tidak berwarna tidak dapat disintesis menjadi CNT, menunjukkan pertumbuhan CNT yang tidak lengkap dengan diameter 38,89 nm. Ini memiliki hasil rendah 4,206% dibandingkan dengan hasil CNT disintesis dari serpih biru dan SR, yang masing-masing mencapai nilai 8,966% dan 11,167%.The study on the suitability of plastic sachet, mainly made of polypropylene (PP), as an alternative source of carbon for the synthesis of carbon nanotubes will be greatly emphasised. Before proceeding with the synthesis of carbon nanotubes (CNT) using plastic sachet, it is imperative to remove the colours that are embedded on them. The removal of colour is done by submerging plastic sachets into hydrogen peroxide (H2O2). H2O2 is readily available and an economically favourable chemical oxidant. CNT production by flame synthesis was attempted. The synthesis makes use of SS 316 as the catalyst substrate, after having undergone oxidative heat treatment, for 30 minutes under 800oC, as the catalyst pre-treatment method. The characterization results of the CNT via XRD, SEM-EDS and TEM, implied that decoloured PP (clear PP) is incapable of being synthesised to CNT. This was further supported with the depiction of incomplete growth of CNT with an average diameter of 38.89nm through its resulting TEM imaging. It produces a low yield of 4.206% in comparison with CNT synthesised from blue and SR flakes, that reaches a value of 8.966% and 11.167% respectively."

"[Dioksin merupakan senyawa berbahaya yang dapat menyebabkan gangguan kulit, hati, hingga menimbulkan kanker. Degradasi dioksin dapat dilakukan oleh mikroorganisme seperti kapang yang menghasilkan enzim ligninolitik. Penelitian bertujuan untuk mendapatkan kapang yang memiliki enzim ligninolitik sehingga berpotensi dalam mendegradasi dioksin. Aktivitas enzim ligninolitik terlihat dari penghilangan warna pada Remazol Brilliant Blue R (RBBR) dan Poly S-119. Metode penelitian meliputi seleksi pada medium padat dan cair, pengukuran aktivitas enzim ligninolitik, serta identifikasi isolat. Seleksi kapang pada medium padat dilakukan dengan medium yang mengandung RBBR dan Poly S-119. Seleksi cair dilakukan dengan mengukur degradasi warna dan aktivitas enzim ligninolitik (lakase, mangan peroksidase, dan lignin peroksidase). Isolat hasilseleksi diidentifikasi molekular 28S rRNA menggunakan primer NL-1 dan NL-4. Hasil seleksi padat menunjukkan sembilan isolat dengan zona degradasi, yaitu FIG- KT-540.1; F-IG-KT-539.2; F-IG-PT-6.3; F-IG-PT 1.16; F-IG-PT-2.14; F-IGPT- 2.5; F-IG-PT-2.7; F-IG-PT-3.1; dan F-IG-PT-2.11. Hasil seleksi cair menunjukkan dua isolat memiliki kemampuan mendegradasi warna tinggi yaitu FIG- KT-540.1 sebesar 59% mendegradasi warna RBBR dan F-IG-PT 1.16 sebesar 85% mendegradasi warna Poly S-119. Isolat F-IG-KT-540.1 dan F-IG-PT 1.16 memiliki aktivitas MnP yang tinggi sebesar 0,0132 dan 0,0186 ΔOD/ml sampel/menit. Identifikasi kedua isolat menunjukkan isolat F-IG-KT-540.1 adalah Aspergillus oryzae dengan nilai bootstrap 99 dan isolat F-IG-PT 1.16 adalah Penicillium charlesii dengan nilai bootstrap 98. Kesimpulan yaitu isolat F-IG-KT-540.1 dan F-IG-PT 1.16 yang memiliki kemampuan tinggi mendegradasi warna berpotensi mendegradasi dioksin. Penelitian lebih lanjut perlu dilakukan untuk mengetahui sinergi antara kedua isolat dalam mendegradasi dioksin.

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Dioxins are harmful compounds which can damage skin, liver, and cause cancer. It can be degraded by microorganisms such as fungi with its ligninolytic enzymes. The research aim was to obtain fungi that has ligninolytic enzymes which potentially degrade dioxin. Activity of ligninolytic enzymes was showed from decolorization of Remazol Brilliant Blue R and Poly S-119 dye. Methods of the research include selection on solid medium and liquid medium, measurement of ligninolytic activity, and identification of fungal isolates. Selection on solid medium was carried out using RBBR and Poly S-119 dye. Selection on liquid medium was carried out through measurement on the color degradation and activity of ligninolytic enzymes (laccase, manganese peroxidase, and lignin peroxidase). The potential isolates in liquid selection medium were identified on 28S rRNA with NL-1 and NL-4 primers. The result showed that nine isolates have

the degradation zone in a solid medium. They were F-IG-KT-540.1; F-IG-KT- 539.2; F-IG-PT-6.3; F-IG-PT 1:16; F-IG-PT-2:14; F-IG-PT-2.5; F-IG-PT-2.7; FIG- PT-3.1; and F-IG-PT-2.11. In liquid selection medium, F-IG-KT-540.1 and FIG-

PT 1.16 isolates showed high capability to degrade dyes. Percentage of RBBR degradation in isolate F-IG-KT-540.1 was 59% and percentage of Poly S-119 degradation in isolate F-IG-PT-1.16 was 85%. Both F-IG-KT-540.1 and F-IG-PT 1.16 isolate have high activity of MnP. Activity of MnP of those isolate were 0,0132 and 0,0186 ΔOD/ml/minutes respectively. The result of identification showed that F-IG-KT-540.1 isolate was Aspergillus oryzae with value of

bootstrap 99 and F-IG-PT-1.16 isolate was Penicillium charlesii with value of bootstrap 98. From this research, F-IG-KT-540.1 and F-IG-PT 1.16 isolates which have capability to degrade dyes potential for degrading dioxin. Further research is needed to determine the synergy between isolates F-IG-KT-540.1 and F-IG-PT- 1.16 to degrade dioxin., Dioxins are harmful compounds which can damage skin, liver, and cause cancer.

It can be degraded by microorganisms such as fungi with its ligninolytic enzymes.

The research aim was to obtain fungi that has ligninolytic enzymes which

potentially degrade dioxin. Activity of ligninolytic enzymes was showed from

decolorization of Remazol Brilliant Blue R and Poly S-119 dye. Methods of the

research include selection on solid medium and liquid medium, measurement of

ligninolytic activity, and identification of fungal isolates. Selection on solid

medium was carried out using RBBR and Poly S-119 dye. Selection on liquid

medium was carried out through measurement on the color degradation and

activity of ligninolytic enzymes (laccase, manganese peroxidase, and lignin

peroxidase). The potential isolates in liquid selection medium were identified on

28S rRNA with NL-1 and NL-4 primers. The result showed that nine isolates have

the degradation zone in a solid medium. They were F-IG-KT-540.1; F-IG-KT-

539.2; F-IG-PT-6.3; F-IG-PT 1:16; F-IG-PT-2:14; F-IG-PT-2.5; F-IG-PT-2.7; FIG-

PT-3.1; and F-IG-PT-2.11. In liquid selection medium, F-IG-KT-540.1 and FIG-

PT 1.16 isolates showed high capability to degrade dyes. Percentage of RBBR

degradation in isolate F-IG-KT-540.1 was 59% and percentage of Poly S-119

degradation in isolate F-IG-PT-1.16 was 85%. Both F-IG-KT-540.1 and F-IG-PT

1.16 isolate have high activity of MnP. Activity of MnP of those isolate were

0,0132 and 0,0186 ΔOD/ml/minutes respectively. The result of identification

showed that F-IG-KT-540.1 isolate was Aspergillus oryzae with value of

bootstrap 99 and F-IG-PT-1.16 isolate was Penicillium charlesii with value of

bootstrap 98. From this research, F-IG-KT-540.1 and F-IG-PT 1.16 isolates which

have capability to degrade dyes potential for degrading dioxin. Further research is

needed to determine the synergy between isolates F-IG-KT-540.1 and F-IG-PT-

1.16 to degrade dioxin.]"

"PET (Polietilena Tereftalat) merupakan kemasan botol plastik berwarna dengan tingkat konsumsi terbesar keempat di dunia. Konsumsi PET di Indonesia meningkat mencapai 7% per tahun hal ini dapat menyebabkan dampak terhadap lingkungan. Penelitian ini bertujuan untuk mendaur ulang limbah PET dengan menggunakan proses sederhana dalam menghilangkan warna dari limbah PET. Hasil penghilangan warna limbah PET akan digunakan sebagai alternatif sumber karbon untuk sintesis carbon nanotube (CNT). Warna limbah PET yang digunakan adalah biru dan hijau. Agen penghilang warna yang terpilih adalah hidrogen peroksida (H­2O2) karena merupakan reagen yang ekonomis dan ramah lingkungan. Limbah PET berwarna dan H2O2 akan dipanaskan ke dalam sistem oil bath pada suhu 110oC dan tekanan 1 atm.Hasil waktu penghilangan warna untuk limbah PET biru lebih cepat dibandingkan limbah PET hijau yaitu 72 dan 115 menit per 15 gram limbah PET. Kualitas penghilangan warna limbah PET biru lebih baik dibanding hasil penghilangan warna limbah PET hijau karena memiliki nilai reflektansi lebih dekat dengan limbah PET tidak berwarna. Proses sintesis CNT dari plastik limbah PET biru yang sudah dihilagkan warnanya menghasilkan yield sebesar 8,58%. Diameter rata rata kristal CNT yang dihasilkan dari proses ini diperoleh sebesar 37 nm. Hal ini menunjukkan bahwa plastik limbah PET yang sudah dihilangkan warnanya dapat digunakan sebagai sumber karbon dalam sintesis CNT.

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The level consumption of Polyethylene Terephthalate (PET) as a packaging of colored beverage bottles occupies the fourth largest in the world. In Indonesia, PET consumption increased reaches 7% per year so that it can cause environmental impacts. This study aims to process the recycling PET waste by obtaining a simple potential process to remove the color from PET waste. The decolorized PET waste will be an alternative carbon source for Carbon Nanotube (CNT) synthesis. The colors of PET waste are blue and green bottles. The selected color removal agent is hydrogen peroxide (H2O2) because it is inexpensive reagent and has lower toxicity to environment. The colored PET waste and H2O2 will be heated in the oil bath system at temperature 110oC and pressure 1 atm.

The result showed that color removal time for blue PET waste faster than the green PET waste, 72 and 115 minutes per 15 grams PET waste. The quality of color removal of blue PET waste is better than the result of color removal of green PET waste because it has a reflectance value closer to colorless PET waste. The CNT synthesis process from plastic blue PET waste which has been color-treated yields a yield of 8.58%. The average diameter of CNT crystals produced from this process is obtained at 37 nm. This shows that PET waste plastic which has been discolored can be used as a carbon source in CNT synthesis."